JPS6042008B2 - Manufacturing method for synthetic resin treated wood - Google Patents
Manufacturing method for synthetic resin treated woodInfo
- Publication number
- JPS6042008B2 JPS6042008B2 JP932380A JP932380A JPS6042008B2 JP S6042008 B2 JPS6042008 B2 JP S6042008B2 JP 932380 A JP932380 A JP 932380A JP 932380 A JP932380 A JP 932380A JP S6042008 B2 JPS6042008 B2 JP S6042008B2
- Authority
- JP
- Japan
- Prior art keywords
- wood
- synthetic resin
- formula
- treated wood
- weight
- 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
Links
- 229920003002 synthetic resin Polymers 0.000 title claims description 22
- 239000000057 synthetic resin Substances 0.000 title claims description 22
- 239000010875 treated wood Substances 0.000 title claims description 15
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 239000002023 wood Substances 0.000 claims description 22
- 150000002148 esters Chemical class 0.000 claims description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 6
- 150000003440 styrenes Chemical class 0.000 claims description 6
- 239000000178 monomer Substances 0.000 claims description 5
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 4
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 3
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 238000005299 abrasion Methods 0.000 description 13
- 150000001875 compounds Chemical class 0.000 description 10
- 238000005336 cracking Methods 0.000 description 5
- 238000005470 impregnation Methods 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- -1 2- Ethylene oxide Chemical compound 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000003505 polymerization initiator Substances 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- 229940095095 2-hydroxyethyl acrylate Drugs 0.000 description 2
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000008602 contraction Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000003827 glycol group Chemical group 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- MMSLOZQEMPDGPI-UHFFFAOYSA-N p-Mentha-1,3,5,8-tetraene Chemical compound CC(=C)C1=CC=C(C)C=C1 MMSLOZQEMPDGPI-UHFFFAOYSA-N 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 239000011120 plywood Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- FVQMJJQUGGVLEP-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOOC(C)(C)C FVQMJJQUGGVLEP-UHFFFAOYSA-N 0.000 description 1
- HGOUNPXIJSDIKV-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)butyl 2-methylprop-2-enoate Chemical compound CCC(CO)(CO)COC(=O)C(C)=C HGOUNPXIJSDIKV-UHFFFAOYSA-N 0.000 description 1
- SYENVBKSVVOOPS-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)butyl prop-2-enoate Chemical compound CCC(CO)(CO)COC(=O)C=C SYENVBKSVVOOPS-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
- GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- APZPSKFMSWZPKL-UHFFFAOYSA-N [3-hydroxy-2,2-bis(hydroxymethyl)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(CO)(CO)CO APZPSKFMSWZPKL-UHFFFAOYSA-N 0.000 description 1
- ZCZFEIZSYJAXKS-UHFFFAOYSA-N [3-hydroxy-2,2-bis(hydroxymethyl)propyl] prop-2-enoate Chemical compound OCC(CO)(CO)COC(=O)C=C ZCZFEIZSYJAXKS-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 230000005865 ionizing radiation Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000007717 redox polymerization reaction Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229920006305 unsaturated polyester Polymers 0.000 description 1
- 210000001215 vagina Anatomy 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Chemical And Physical Treatments For Wood And The Like (AREA)
Description
【発明の詳細な説明】
Lマιn口・ ・ れ−・・・ィーナzえトμm1デ
/ れ、4トヨ号媚■云力几P狙木材の製造法に関する
。[Detailed description of the invention]
/ Re: 4 Toyo No. 4 Concerning the method of manufacturing Toyo P target lumber.
木材は入手しやすいこと。Wood is easy to obtain.
工作が容易てあること、比重が小さいこと、強度が大き
いこと、熱伝導度が小さいこと、比熱が大きいこと、音
や機械振動の吸収性能が良好てあること等、他の材料て
は得られない特有な性質を有している。反面、水分の吸
収や乾燥により膨張や収縮をするためにそりやひずみが
生じたり、また耐摩耗性に劣る等の欠点を有している。
このような木材の持つている吸湿性に伴う膨張、収縮を
改善して寸法安定性を付与するとともに耐摩耗性および
強度を向上させる手段として、従来よりスチレン、メチ
ルメタクリレート、不飽和ポリエステル等のラジカル重
合性化合物を木材に含浸あるいは塗布したのち重合・さ
せて木材の性質を改良する合成樹脂処理木材の製造法は
公知である。合成樹脂の含浸あるいは塗布により木材の
性質は強度、寸法安定性、耐摩耗性、耐腐朽性が改良さ
れ、さらに重量感、美観等の二次的な特徴が付与される
。しかしながら、こフれら諸特徴を有する合成樹脂処理
木材の大きな欠点は、経年変化でクラックが発生し、さ
らにこのクラックの発生は寒暖の差が大きな条件下で助
長されることである。このクラックの発生は、合成樹脂
の含浸あるい5は塗布による木材中の内部応力の増加が
原因とえられるところから、合成樹脂処理木材の宿命的
性質と従来より考えられており、適切なりラック発生防
止方法は今まで見いだされていなかつた。It is easy to work with, has low specific gravity, high strength, low thermal conductivity, high specific heat, and has good absorption performance for sound and mechanical vibration, etc., which cannot be obtained with other materials. It has unique properties. On the other hand, it has drawbacks such as warpage and distortion due to expansion and contraction due to moisture absorption and drying, and poor abrasion resistance.
Radicals such as styrene, methyl methacrylate, and unsaturated polyester have traditionally been used as a means of improving the expansion and contraction caused by the hygroscopicity of wood, giving it dimensional stability, and improving its abrasion resistance and strength. A method for producing synthetic resin-treated wood is known, in which wood is impregnated or coated with a polymerizable compound and then polymerized to improve the properties of the wood. Impregnation or coating with synthetic resins improves the properties of wood, such as strength, dimensional stability, abrasion resistance, and rot resistance, and also imparts secondary characteristics such as weight and aesthetics. However, a major drawback of synthetic resin-treated wood having these characteristics is that cracks occur due to aging, and the occurrence of cracks is further aggravated under conditions with large temperature differences. The occurrence of cracks is thought to be caused by an increase in internal stress in the wood due to impregnation or application of synthetic resin, and has traditionally been considered to be a fateful property of synthetic resin-treated wood. Until now, no method has been found to prevent this from occurring.
ただ一部において、合成樹脂の含浸または塗布量を重量
増加率で10ないし2唾量%程度の少量にすることによ
つてクラック発生を防止する方法が試みられているが、
この方法ではクラックの発生はある程度防止できても、
合成樹脂の含浸または塗布量が少ないため、合成樹脂処
理木材に本来要求される強度、寸法安定性および耐摩耗
性が不十分てある。本発明者らは前記のような欠点を改
良した合成樹脂処理木材の製造法について鋭意研究を行
なつた結果、スチレン誘導体、モノアクリル酸エステル
またはモノメタクリル酸エステルにポリオキシアルキレ
ングリコール鎖をもつビニル系単量体を配合した処理液
を木材に含浸させたのち硬化させることによつて、合成
樹脂処理木材本来の特性をそこなうことなくクラックの
発生が防止されることを見いた七、本発明にいたつた。However, some attempts have been made to prevent the occurrence of cracks by reducing the amount of synthetic resin impregnated or applied to a small amount of about 10 to 2% by weight increase rate.
Although this method can prevent cracks to some extent,
Because the amount of synthetic resin impregnated or applied is small, the strength, dimensional stability, and abrasion resistance originally required of synthetic resin-treated wood are insufficient. The present inventors have conducted intensive research on a method for producing synthetic resin-treated wood that improves the above-mentioned drawbacks, and as a result, we have found that vinyl having polyoxyalkylene glycol chains in styrene derivatives, monoacrylic esters, or monomethacrylic esters has been developed. It was found that by impregnating wood with a treatment solution containing a series monomer and then curing it, the occurrence of cracks can be prevented without impairing the inherent properties of synthetic resin-treated wood. It was it.
すなわち、本発明はつぎの一般式
(ここて、Rは水素原子またはメチル基、mは2ないし
4の整数、nは2ないし20の整数である。That is, the present invention is based on the following general formula (where R is a hydrogen atom or a methyl group, m is an integer of 2 to 4, and n is an integer of 2 to 20.
)で示されるポリオキシアルキレングリコールモノアク
リレートおよびポリオキシアルキレン5グリコールモノ
メタクリレートから選ばれた1種または2種以上を30
ないし6呼量%、スチレン誘導体、〔1〕式以外のモノ
アクリル酸エステル、およびモノメタクリル酸エステル
から選ばれた1種または2種以上を40ないし7呼量%
含有する処3理液を木材に含浸させたのち硬化させるこ
とを特徴とする合成樹脂処理木材の製造法である。〔1
〕式化合物は、アクリル酸、メタクリル酸、2−ヒドロ
キシエチルアクリレート、2−ヒドロキシエチルメタク
レート、2−ヒドロキシプ4口ビルアクリレート、2−
ヒドロキシプロピルメタクリレート等に、三フッ化ホウ
素、四塩化スズ等のカチオン系化合物の存在下、エチレ
ンオキシド、プロピレンオキシド、ブチレンオキシド、
テトラヒドロフラン等のアルキレンオキシドの1種また
は2種以上を付加重合させるか、アクリル酸あるいはメ
タクリル酸とポリエチレングリコール、ポリプロピレン
グリコール、ポリブチレングリコール等のポリアルキレ
ングリコールとをエステル化反応させて得られる。〔1
〕式化合物のアルキレンオキシドの付加モル数を2ない
し20モルに限定したのは、20モルを越えると〔1〕
式化合物が高分子量化するために)木材への含浸率が低
下して硬化させた場合にその効果を期待できず、さらに
ポリオキシアルキレングリコール鎖の可塑剤的効果によ
り強度および耐摩耗性が低下することによる。) One or more selected from polyoxyalkylene glycol monoacrylate and polyoxyalkylene 5-glycol monomethacrylate shown in 30
40 to 7% by volume of one or more selected from styrene derivatives, monoacrylic esters other than formula [1], and monomethacrylic esters.
This is a method for producing synthetic resin-treated wood, which is characterized by impregnating wood with the three treatment solutions contained therein and then curing it. [1
] Compounds of the formula include acrylic acid, methacrylic acid, 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, 2-hydroxypterobyl acrylate, 2-
Ethylene oxide, propylene oxide, butylene oxide,
It can be obtained by addition polymerizing one or more alkylene oxides such as tetrahydrofuran, or by esterifying acrylic acid or methacrylic acid with a polyalkylene glycol such as polyethylene glycol, polypropylene glycol, or polybutylene glycol. [1
] The reason why the number of moles of alkylene oxide added in the formula compound is limited to 2 to 20 moles is that if it exceeds 20 moles, [1]
Due to the high molecular weight of the formula compound), the impregnation rate into wood decreases and the effect cannot be expected when hardened, and furthermore, the strength and abrasion resistance decrease due to the plasticizer effect of the polyoxyalkylene glycol chain. By doing.
また、アルキレンオキシドの付加モル数が2モル未満で
は十分なりラック発生防止能が図れないためである。ス
チレン誘導体、〔1〕式以外のモノアクリル酸エステル
およびモノメタクリル酸エステルとしては、たとえば、
スチレン、α−メチルスチレン、p−メチルーα−メチ
ルスチレン、グリシジルアクリレート、グリシジルメタ
クリレート、メチルアクリレート、メチルメタクリレー
ト、エチルアクリレート、エチルメタクリレート、ブチ
ルアクリレート、ブチルメタクリレート、2−エチルヘ
キシルアクリレート、2−エチルヘキシルメタクリレー
ト、2−ヒドロキシエチルアクリレート、2−ヒドロキ
シエチルメタクリレート、2一ヒドロキシプロピルアク
リレート、2−ヒドロキシプロピルメククリレート、ト
リメチロールプロパンモノアクリレート、トリメチロー
ルプロパンモノメタクリレート、ペンタエリスリトール
モノアクリレート、ペンタエリスリトールモノメタクリ
レート等がある。Further, if the number of moles of alkylene oxide added is less than 2 moles, it is insufficient and the ability to prevent rack generation cannot be achieved. Examples of styrene derivatives, monoacrylic esters and monomethacrylic esters other than formula [1] include:
Styrene, α-methylstyrene, p-methyl-α-methylstyrene, glycidyl acrylate, glycidyl methacrylate, methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, butyl acrylate, butyl methacrylate, 2-ethylhexyl acrylate, 2-ethylhexyl methacrylate, 2 -Hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl acrylate, 2-hydroxypropyl meccrylate, trimethylolpropane monoacrylate, trimethylolpropane monomethacrylate, pentaerythritol monoacrylate, pentaerythritol monomethacrylate, and the like.
木材に含浸させる処理液における〔1〕式化合物の含有
率は30ないし6呼量%てあり、3呼量%未満ではクラ
ック発生防止能が小さく、6呼量%を越えるとクラック
発生防止能は期待てきても合成樹脂処理木材に要求され
る耐摩耗性および硬度が期待できない。The content of the compound of formula [1] in the treatment solution to be impregnated into wood is 30 to 6% by weight, and if it is less than 3% by weight, the ability to prevent cracking is small, and if it exceeds 6% by weight, the ability to prevent cracking is poor. Despite our high expectations, we cannot expect the abrasion resistance and hardness required of synthetic resin treated wood.
木材に含浸させた〔1〕式化合物を30ないし60重量
%含有する処理液を硬化させるためには、含浸した木材
を50′C以上に加熱して処理液を熱重合させたり、電
離放射線、電子線、紫外線等で重合させて硬化すること
も可能であるが、通常は重合開始剤を用いて重合させる
ことが好ましい。In order to cure the treatment liquid containing 30 to 60% by weight of the compound of formula [1] impregnated into wood, the impregnated wood is heated to 50'C or higher to thermally polymerize the treatment liquid, or ionizing radiation, Although it is possible to polymerize and cure with electron beams, ultraviolet rays, etc., it is usually preferable to polymerize using a polymerization initiator.
この楊合に用いる重合開始剤としては、ビニル基を重合
させる能力を有する過酸化物や、過酸化物と還元剤を組
み合わせたレドックス系重合開始剤がある。さらに必要
であれば、アミン、金属セッケン等に代表される公知の
重合促進剤を加えて硬化させることも可能である。本発
明に用いる〔I〕式化合物を30なι化6喧量%とスチ
レン誘導体、〔I〕式以外のアクリル酸エステルおよび
メタクリル酸エステルから選ばれた単量体の1種または
2種以上を40〜7鍾量%含有する処理液は、木の種類
や木材の形態(材木、単板、合板等)を問わず、あらゆ
る木材に適用てきる。Examples of the polymerization initiator used in this reaction include peroxides having the ability to polymerize vinyl groups and redox polymerization initiators that are a combination of peroxides and reducing agents. Furthermore, if necessary, it is also possible to add a known polymerization accelerator such as amine, metal soap, etc. for curing. The compound of the formula [I] used in the present invention is mixed with 6% of a 30-N compound and one or more monomers selected from styrene derivatives, acrylic esters and methacrylic esters other than those of the formula [I]. A treatment liquid containing 40 to 7% by weight can be applied to all kinds of wood, regardless of the type of wood or the form of the wood (timber, veneer, plywood, etc.).
本発明の方法て得られる合成樹脂処理木材は、強度とク
ラック発生のないことがとくに要求される高級建築用木
材、外壁用木材、床材、スポーツ用品用材料等に利用す
ることができる。The synthetic resin-treated wood obtained by the method of the present invention can be used as high-grade architectural wood, wood for exterior walls, flooring materials, materials for sports equipment, etc., which particularly require strength and no cracking.
以下、実施例により本発明を説明する。The present invention will be explained below with reference to Examples.
実施例
〔I〕式化合物を含有する処理液および従来から使われ
ている処理液を用いて木材の処理を行なつた。Example [I] Wood was treated using a treatment solution containing the compound of formula [I] and a conventional treatment solution.
第1表に用いた処理液の組成を示す。Table 1 shows the composition of the treatment liquid used.
第1表
木材の合成樹脂処理試験片の調製:基材となる木材は厚
さ0.6顛、比重0.44ないし0.47、繊維方向の
長さ30C7n1直角方向の長さWOの米松製単板を用
いた。Table 1: Preparation of synthetic resin treated wood specimens: The base wood is made of Yonematsu with a thickness of 0.6 mm, a specific gravity of 0.44 to 0.47, a length in the fiber direction of 30C7N1 and a length in the right angle direction of WO. A veneer was used.
この単板を1%の有機過酸化物(tーブチルパーオキシ
ー2−エチルヘキサノエート)を含む処理液中に浸漬し
て約10k9/C!lの圧力下で10分間含浸処理を行
なつたのち、圧力を常圧にもどしてから単板を含浸液よ
り引き上けた。単板表面の含浸液がたれなくなつてから
、単板をアルミニウムホイルでつつみ、100らCで3
紛間硬化処理を行なつた。この合成樹脂処理単板をエリ
ア樹脂接着剤を均一に塗布したラワン製クプライ合板上
に接着し、120℃、10k9/Cliの条件下で2分
間熱圧して試験片を調製した。合成樹脂処理単板の重量
増加率:つぎの式により求めた。This veneer was immersed in a treatment solution containing 1% organic peroxide (t-butylperoxy-2-ethylhexanoate) and the result was approximately 10k9/C. After impregnation treatment was carried out for 10 minutes under a pressure of 1 liter, the pressure was returned to normal pressure and the veneer was lifted out of the impregnating solution. After the impregnation liquid on the surface of the veneer stops dripping, wrap the veneer with aluminum foil and heat it at 100 °C for 3
A dust hardening treatment was performed. This synthetic resin-treated veneer was adhered to Lauan's Cuply plywood to which an area resin adhesive was evenly applied, and hot-pressed for 2 minutes at 120° C. and 10k9/Cli to prepare a test piece. Weight increase rate of synthetic resin treated veneer: Calculated using the following formula.
W1:未処理単板の重量
W2:合成樹脂処理単板の重量
調製した試験片について、クラック発生試験、摩耗試験
および硬度試験を行なつた。W1: Weight of untreated veneer W2: Weight of synthetic resin-treated veneer The prepared test pieces were subjected to a crack generation test, an abrasion test, and a hardness test.
クラック発生試験:調製した試験片を繊維方向の長さ5
cmに切断したものを用い、寒熱サイクル3テストによ
り行なつた。Crack generation test: The length of the prepared test piece in the fiber direction is 5
The sample was cut into cm pieces and subjected to 3 cold/heat cycle tests.
すなわち、−20℃で2橋間、ついて80行C0Cで2
楊間の静置を1サイクルとし、クラックが発生するまで
のサイクル数を求めた。摩耗試験:調製した試験片を1
0C77!×10C77!の大き,さに切断したものを
用い、テーベ摩耗試験機により実施した。That is, 2 bridges at -20℃, then 2 at 80 lines C0C.
The number of cycles until cracking was determined was determined by allowing one cycle to stand between the paper towels. Abrasion test: The prepared test piece was
0C77! ×10C77! The test was carried out using a Thebe abrasion tester using a piece cut to the size of .
試験結果は試験片の全摩耗損失量で示す。試験条件
1摩耗試験紙:ーS−33サンドベーパーー2荷重:片
側500g1全荷重1000g3摩耗回数:500回硬
度試験:調製した試験片を繊維方向の長さ50に切断し
たものを用い、JIS−Z−2117−63木材のかた
さ試験方法に準じて実施した。The test results are expressed as the total abrasion loss of the test piece. Test conditions 1 Abrasion test paper: - S-33 Sand Vapor - 2 Load: 500 g on each side 1 Total load 1000 g 3 Number of wear: 500 times Hardness test: Using the prepared test piece cut into lengths in the fiber direction, JIS- The test was carried out according to Z-2117-63 wood hardness test method.
試験結果フは3個の測定値の平均を示す。試験結果を第
2表に示す。The test results show the average of three measurements. The test results are shown in Table 2.
試験慟.8〜10(本発明例)は試験?.1〜7に比較
して、それぞれクラック発生までのサイクル数が大きく
てクラックを発生しにくいことを示して.いる。Examination vagina. 8 to 10 (invention examples) are tests? .. Compared to No. 1 to No. 7, each number of cycles until cracking is larger, indicating that cracks are less likely to occur. There is.
全摩耗損失と硬度の低下はわずかであり、合成樹脂処理
木材として適している。〔1〕式化合物を多く使用した
試験NOl2〜13は、クラックは発生しにくいが全摩
耗損失が大きくて合成樹脂処理木材として不適当てある
。Total abrasion loss and hardness decrease are small, making it suitable for synthetic resin treated wood. Test Nos. 2 to 13, in which a large amount of the compound of the formula [1] was used, were less likely to cause cracks, but the total abrasion loss was large, making them unsuitable for use as synthetic resin-treated wood.
Claims (1)
〕(ここで、Rは水素原子またはメチル基、mは2ない
し4の整数、nは2ないし20の整数である。 )で示されるポリオキシアルキレングリコールモノアク
リレートおよびポリオキシアルキレングリコールモノメ
タクリレートから選ばれた1種または2種以上30ない
し60重量%とスチレン誘導体、〔 I 〕式以外のモノ
アクル酸エステルおよびモノメタクリル酸エステルから
選ばれた単量体の1種または2種以上40ないし70重
量%とを含有する処理液を木材に含浸させたのち硬化さ
せることを特徴とする合成樹脂処理木材の製造法。2
スチレン誘導体、〔 I 〕式以外のモノアクリル酸およ
びモノメタクリル酸エステルから選ばれた単量体がメチ
ルアクリレート、メチルメタクリレートまたはスチレン
である特許請求の範囲第1項記載の合成樹脂処理木材の
製造法。[Claims] 1. General formula▲There are mathematical formulas, chemical formulas, tables, etc.▼・・・・・・〔I
] (wherein R is a hydrogen atom or a methyl group, m is an integer of 2 to 4, and n is an integer of 2 to 20.) selected from polyoxyalkylene glycol monoacrylate and polyoxyalkylene glycol monomethacrylate represented by 30 to 60% by weight of one or more monomers selected from styrene derivatives, monoacrylic esters and monomethacrylic esters other than formula [I], and 40 to 70% by weight of one or more monomers selected from 1. A method for producing synthetic resin-treated wood, which comprises impregnating wood with a treatment solution containing and then curing the wood. 2
The method for producing synthetic resin-treated wood according to claim 1, wherein the monomer selected from styrene derivatives, monoacrylic acids and monomethacrylic esters other than formula [I] is methyl acrylate, methyl methacrylate, or styrene. .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP932380A JPS6042008B2 (en) | 1980-01-31 | 1980-01-31 | Manufacturing method for synthetic resin treated wood |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP932380A JPS6042008B2 (en) | 1980-01-31 | 1980-01-31 | Manufacturing method for synthetic resin treated wood |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56106809A JPS56106809A (en) | 1981-08-25 |
| JPS6042008B2 true JPS6042008B2 (en) | 1985-09-19 |
Family
ID=11717257
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP932380A Expired JPS6042008B2 (en) | 1980-01-31 | 1980-01-31 | Manufacturing method for synthetic resin treated wood |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6042008B2 (en) |
-
1980
- 1980-01-31 JP JP932380A patent/JPS6042008B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56106809A (en) | 1981-08-25 |
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