JPS5926203A - Surface treating method for wood - Google Patents

Surface treating method for wood

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Publication number
JPS5926203A
JPS5926203A JP13576582A JP13576582A JPS5926203A JP S5926203 A JPS5926203 A JP S5926203A JP 13576582 A JP13576582 A JP 13576582A JP 13576582 A JP13576582 A JP 13576582A JP S5926203 A JPS5926203 A JP S5926203A
Authority
JP
Japan
Prior art keywords
weight
wood
emulsion
latex
coating film
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
Application number
JP13576582A
Other languages
Japanese (ja)
Inventor
伊藤 孝顕
卓弘 後藤
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.)
Mitsubishi Petrochemical Co Ltd
Original Assignee
Mitsubishi Petrochemical Co Ltd
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 Mitsubishi Petrochemical Co Ltd filed Critical Mitsubishi Petrochemical Co Ltd
Priority to JP13576582A priority Critical patent/JPS5926203A/en
Publication of JPS5926203A publication Critical patent/JPS5926203A/en
Pending legal-status Critical Current

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  • Application Of Or Painting With Fluid Materials (AREA)
  • Chemical And Physical Treatments For Wood And The Like (AREA)

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】 本発明はパレットのデツキボード、壁拐、橋桁月等に用
いる木材の表面処理方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for surface treatment of wood used for pallet deck boards, wall coverings, bridge girders, etc.

ドラム罐、コンテナー等をフ{−クリットで移送するの
にパレットが使用されており、このノくレッ1・とじて
は木製のものが主流を占めている。
Pallets are used to transport drums, containers, etc. using pallets, and the majority of these pallets are made of wood.

木製パレットは摩擦係数が大きく、積まれた荷物が滑シ
落ち難いこと及び利用価値がなくなった後の焼却が容易
であること等の利点を有する反面、防水性に乏しく、雨
水によって腐ったり、乾燥によって木質中に含まれてい
た水分が過剰に逸散してデツキボードが反ったり、ひび
割れを生ずる欠点があり、その寿命は2〜3年である。
Wooden pallets have the advantage of having a large coefficient of friction, making it difficult for loaded cargo to slip off, and making it easy to incinerate once they are no longer useful. This has the disadvantage that the moisture contained in the wood is excessively dissipated, causing the deck board to warp or crack, and its lifespan is only 2 to 3 years.

このような木製パレットの欠点を改良したものとして、
鉄材補強発泡プラスチック製パレットが市販されておシ
、この鉄材補強発泡グラスチック製のものは耐水性及び
耐薬品性に優れているが、焼却性の問題と高価格なため
、硫酸等の化学薬品分野等、特殊な分野にのみ使用され
ているのが現状であって、その需要が伸び悩んでいるの
が実情である。
As an improvement on the shortcomings of wooden pallets,
Pallets made of steel-reinforced foamed plastic are commercially available. Although pallets made of steel-reinforced foamed plastic have excellent water and chemical resistance, they have problems with incineration and are expensive, so they cannot be used with chemicals such as sulfuric acid. The reality is that they are only used in special fields, such as fields, and the demand for them is sluggish.

そこで、木材に耐水性を付与したり、水分の乾燥を防止
する目的で木材表面に塗料を塗布含浸させ、加熱乾燥し
て塗膜を形成する方法(例えば、特開昭49−1348
04号公報や特開昭51− 76405号公報)である
とか、木材に重合性ビニル単量体や不飽和ポリエステル
樹脂を含浸させ、加熱重合させる方法が提案されている
。 ところが、これらの溶剤型の塗料や油性の重合性j
l’t ’n3体を用いる方法では含浸に長時間を必要
とする欠点がある。
Therefore, in order to impart water resistance to wood or prevent water from drying out, there is a method of applying paint to the wood surface, impregnating it, and heating and drying it to form a coating film (for example, Japanese Patent Application Laid-Open No. 49-1348
04 and JP-A-51-76405), a method has been proposed in which wood is impregnated with a polymerizable vinyl monomer or unsaturated polyester resin and then heated and polymerized. However, these solvent-based paints and oil-based polymerizable paints
The method using l't'n3 bodies has the disadvantage that impregnation requires a long time.

このような含浸の欠点を改仰する目的で、例えば、特開
昭55−71501号公報に見られる如く、sBRラテ
ックスまだはエチレン・酢酸ビニル共重合体水性エマル
ション等の最低造膜温度が0〜40℃の水性分散液を木
材表面に塗布含浸させ、常温で乾燥させて木材表面に水
蒸気透過率が1日当り10〜100 ’/、、/ノ塗膜
を設ける方法が提案されている。 この方法で得られた
処理木(」は干し割れの発生が少ない利点を有するが、
パレットのデツキボードとして用いたときには機械的強
度が乏しく、積載される荷物との摩擦によって塗膜が摩
滅し易いといった欠点がある。 更にまだ、ゴムラテッ
クスまたはエマルションのコムないし樹脂の種類によっ
ては、得られる塗膜力積1薬品性に乏しいといった問題
がある。
In order to overcome these drawbacks of impregnation, for example, as seen in JP-A-55-71501, sBR latex and ethylene-vinyl acetate copolymer aqueous emulsions have a minimum film-forming temperature of 0 to 0. A method has been proposed in which a wood surface is coated with an aqueous dispersion at 40 DEG C. and then dried at room temperature to form a coating film having a water vapor transmission rate of 10 to 100'/day/day. The treated wood obtained by this method has the advantage of less occurrence of drying cracks, but
When used as a pallet deck board, the mechanical strength is poor, and the coating film is easily worn away by friction with loaded cargo. Furthermore, depending on the type of rubber latex or emulsion comb or resin, there are problems such as poor coating force and poor chemical properties.

本発明は、従来のゴムラテックスまたは樹脂水性エマル
ジョンの上記欠点を全面的に解消し、面1摩滅性及び耐
薬品性に富んだ塗膜を表面に形成できる木材の表面処理
方法の提供を企図したものであって、その要旨とすると
ころは、ゴムラテックスと加硫剤と樹脂水性エマルジョ
ンを含有する水性分散液を木材表面に塗布した後、乾燥
させ、次いで加熱して加硫反応を行なわせて、木材表面
上に塗膜を形成することにある。
The present invention aims to provide a wood surface treatment method that completely eliminates the above-mentioned drawbacks of conventional rubber latex or resin aqueous emulsions and can form a coating film on the surface that is highly abrasion resistant and chemical resistant. The gist of this is that an aqueous dispersion containing rubber latex, a vulcanizing agent, and an aqueous resin emulsion is applied to the wood surface, dried, and then heated to cause a vulcanization reaction. , to form a coating film on the wood surface.

本発明の適用される木材としては、米っが、ラワン、チ
ーク、マホガニー、杉及び松等が挙げられ、その木材形
状はパレットのデツキボード用には板状体が好ましいが
、用途によっては角柱状や丸棒状でもよい。 パレット
のデツキボードとしては、一般にラワン、集成材及び米
っが等の板状体が使用される。 この木材の表面に塗布
含浸される水性分散液はゴムラテックスと該ゴムラテッ
クス中のゴムを加硫する加硫剤と樹脂水性エマルジョン
を少なくとも含有することが要件である。
Wood to which the present invention can be applied include rice bran, lauan, teak, mahogany, cedar, and pine, and the shape of the wood is preferably a plate for pallet deck boards, but depending on the use, it may be prismatic. It may also be in the shape of a round bar. Generally, plate-shaped materials such as lauan, laminated wood, and rice cake are used as deck boards for pallets. The aqueous dispersion applied and impregnated onto the surface of the wood must contain at least rubber latex, a vulcanizing agent for vulcanizing the rubber in the rubber latex, and an aqueous resin emulsion.

上記ゴムラテックスとしては、天然ゴムラテックス、ニ
トリルゴムラテックス、ブチルゴムラテックスの他に、
脂肪族共役ジオ2フ1フ25〜フ5重量%とこれと他の
嘔量体、例えばアルケニル芳香族単量体、エチレン性不
飽和J%L、 g体との共重合体のゴム質の水性分散液
を用いることができる。
In addition to natural rubber latex, nitrile rubber latex, and butyl rubber latex, examples of the above-mentioned rubber latex include
A rubbery copolymer of 25 to 5% by weight of aliphatic conjugated di-2F1 and other polymers, such as alkenyl aromatic monomers, ethylenically unsaturated J%L, and Aqueous dispersions can be used.

そして、脂肪族共役ジオレフィンとしてはブタジェン、
イソブチレン、クロロプレン等が、アルケニル芳香族単
量体としてはスチレン、ジビニルベンゼン、メチルスチ
レン等が、また、エチレン性不飽和単量体としてはアク
リル酸メチル、アクリル酸プロピル、アクリル酸n・ブ
チル、アクリル酸t・ブチル、アクリル酸2−エチルヘ
キシル、メタクリル酸メチル、メタクリル酸エチル、ア
クリロニトリル、メタクリレートリル、塩化ビニル、塩
化ビニリデン、酢酸ビニル、アクリル酸、メタクリル酸
・エチレン等であって、具体的には、スチレン・ブタジ
ェン系共重体ラテックス(例えばブタジェン33重量%
、スチレン65重量%、アクリル酸2重量%よりなる共
重合体ラテックス)、アクリロニトリル・ブタジェン系
共重合体ラテックス(例えばアクリロニトリル38重1
%、ブタシェフ62重量%よりなる共重合体ラテックス
)、メチルメタクリレート・ブタジェン系共重合体ラテ
ックス(例えばメチルメタクリレート42重量%、ブタ
ジェン58重量%よりなる共重合体ラテックス)、その
他ポリイソブチレン系共重合体ラテックス、ポリクロロ
プレン系共重合体ラテックス等の合成ゴム系共重合体が
挙げられる。
And as aliphatic conjugated diolefins, butadiene,
Isobutylene, chloroprene, etc., alkenyl aromatic monomers include styrene, divinylbenzene, methylstyrene, etc., and ethylenically unsaturated monomers include methyl acrylate, propyl acrylate, n-butyl acrylate, acrylic. t-butyl acid, 2-ethylhexyl acrylate, methyl methacrylate, ethyl methacrylate, acrylonitrile, methacrylate trile, vinyl chloride, vinylidene chloride, vinyl acetate, acrylic acid, methacrylic acid/ethylene, etc., specifically, Styrene-butadiene copolymer latex (e.g. butadiene 33% by weight)
, copolymer latex consisting of 65% by weight of styrene and 2% by weight of acrylic acid), acrylonitrile-butadiene copolymer latex (e.g., 38% by weight of acrylonitrile, 1% by weight of acrylonitrile)
%, copolymer latex consisting of 62% by weight of Butashev), methyl methacrylate/butadiene copolymer latex (for example, copolymer latex consisting of 42% by weight of methyl methacrylate and 58% by weight of butadiene), and other polyisobutylene copolymers. Examples include synthetic rubber copolymers such as latex and polychloroprene copolymer latex.

次に加硫剤としては、硫黄、チオグリコール酸、ジクミ
ルパーオキザイド、キノンジオキシム、無水マレイン酸
、亜鉛華、或いはメチロールメラミン樹脂等を用いるこ
とができる。 そして、上記加硫剤の配合量はゴムラテ
ックス中のゴム質の二重結合の数に依存するが、通常は
ゴムラテックスの固形分の1〜20重量%、好ましくは
5〜10重重%の割合で用いる。
Next, as the vulcanizing agent, sulfur, thioglycolic acid, dicumyl peroxide, quinone dioxime, maleic anhydride, zinc white, or methylolmelamine resin can be used. The amount of the vulcanizing agent added depends on the number of rubbery double bonds in the rubber latex, but it is usually 1 to 20% by weight, preferably 5 to 10% by weight of the solid content of the rubber latex. used in

更に、樹脂水性エマルジョンとしては、前記アルケニル
芳香族単量体もしくはエチレン性不飽和単量体のホモ重
合体、或いはこれら二種以上の単量体の共重合体、また
はこれら単量体とイタコン酸、無水マレイン酸、フマル
酸等の不飽和多塩基酸との共重合体等の熱可塑性樹脂の
水性エマルジョンを用いることができる。 そして、具
体的にハ、酢酸ビニル重合体エマルジョン、エチレン・
酢酸ビニル系共重合体エマルジョン、アクリル酸エステ
ル系共重合体エマルジョン、スチレン0アクリル酸工ス
テル系共重合体エマルジョン、その他アクリル酸エステ
ル・酢酸ビニル系共重合体エマルジョン、塩化ビニル重
合体エマルジョン、塩化ビニル・塩化ビニリデン系共重
合体エマルジョン、スチレン・アクリル酸n・ブチル−
イタコン酸共重合体エマルジョン等が挙げられる。
Furthermore, the aqueous resin emulsion may be a homopolymer of the alkenyl aromatic monomer or ethylenically unsaturated monomer, a copolymer of two or more of these monomers, or a combination of these monomers and itaconic acid. An aqueous emulsion of a thermoplastic resin such as a copolymer with an unsaturated polybasic acid such as , maleic anhydride, or fumaric acid can be used. Specifically, c) vinyl acetate polymer emulsion, ethylene/vinyl acetate polymer emulsion,
Vinyl acetate copolymer emulsion, acrylic ester copolymer emulsion, styrene-0 acrylic ester copolymer emulsion, other acrylic ester/vinyl acetate copolymer emulsion, vinyl chloride polymer emulsion, vinyl chloride・Vinylidene chloride copolymer emulsion, styrene/n-butyl acrylate-
Examples include itaconic acid copolymer emulsion.

本発明で用いるゴムラテックスは、塗布乾燥後、加熱さ
れ、機械的強度の高い、かつ、滑り市め効果の塗膜を形
成する上に役立ち、一方、樹脂水性エマルジョンは塗膜
に可撓性、耐#Ri撃性及び耐候性を伺与する。 しか
して、ゴムラテックスと樹脂水性エマルジョンの配合割
合は、固形分重量比あって、し3未満であると、得られ
る塗膜が衝撃に脆く、かつ、滑り易くなるし、逆に′:
+1を越えると、滑り止め効果は十分であるが、塗膜が
傷つき易く、かつ、耐候性及び木材との密着性が悪くな
る。 また、樹脂水性エマルジョンの濃度は固形分換算
で10〜65重量%、好ましくは25〜50重量%であ
シ、その最低造膜温度は乾燥性の面から0〜30℃が好
ましい。
The rubber latex used in the present invention is heated after application and drying, and is useful for forming a coating film with high mechanical strength and a sliding effect, while the aqueous resin emulsion gives the coating film flexibility and Investigates #Ri impact resistance and weather resistance. However, if the blending ratio of rubber latex and aqueous resin emulsion is less than 3 based on the solid content weight ratio, the resulting coating film will be brittle and slippery against impact;
If it exceeds +1, the anti-slip effect will be sufficient, but the coating will be easily damaged and the weather resistance and adhesion to wood will deteriorate. Further, the concentration of the aqueous resin emulsion is 10 to 65% by weight, preferably 25 to 50% by weight in terms of solid content, and the minimum film forming temperature thereof is preferably 0 to 30°C from the viewpoint of drying properties.

本発明を実施する場合には、主要3成分であるゴムラテ
ックス、加硫剤、樹脂水性エマルジョンの他に酸化チタ
ン、カーボンブランク、弁から等の顔料、クレイ、炭酸
カルシウム等の充填剤、レベリング剤、紫外線吸収剤等
を上記主要3成分よりなる水性分散液に配合してもよく
、この水性分散液を木材表面上に塗布含浸させる手段と
しては浸漬法、ロール法、ブレード法またはスプレー法
等が用いられ、これらの方法は木材の形状や水性分散液
の塗布量に応じて選択される。
When carrying out the present invention, in addition to the three main components of rubber latex, a vulcanizing agent, and an aqueous resin emulsion, titanium oxide, carbon blank, pigments such as valves, clay, fillers such as calcium carbonate, and leveling agents are used. , ultraviolet absorbers, etc. may be blended into the aqueous dispersion consisting of the above three main components, and methods for coating and impregnating the surface of the wood with this aqueous dispersion include dipping, roll, blade, and spray methods. These methods are selected depending on the shape of the wood and the amount of aqueous dispersion applied.

水性分散液の塗布量は80〜1000〜(固形分換算)
、好ましくは150〜600へであり、この水性分散液
が塗布含浸された木材は0〜65℃で乾燥され、次いで
100〜170℃に加熱されてコ゛ムの加硫反応が行な
われ、木材表面上に連続塗膜を形成できる。 この塗膜
が表面に形成された木材は耐水性、耐衝撃性、耐候性、
耐摩滅性に優れ、かつ、滑す摩擦が大きいので、特にパ
レットのデ・ツキボードとして用いた場合の効果は顕著
である。
The amount of aqueous dispersion applied is 80~1000~ (solid content equivalent)
, preferably from 150 to 600°C, and the wood coated and impregnated with this aqueous dispersion is dried at 0 to 65°C, then heated to 100 to 170°C to perform a vulcanization reaction of the comb, and the wood surface is coated with Can form a continuous coating film. Wood with this coating formed on its surface has water resistance, impact resistance, weather resistance,
Because it has excellent abrasion resistance and high sliding friction, it is particularly effective when used as a de-push board for pallets.

以下、実施例により本発明を更に詳細に説明する。Hereinafter, the present invention will be explained in more detail with reference to Examples.

実施例1 ブタジェン33重量部、メチレフ65重計部、アクリル
酸2レフ部、過硫酸ナトリウム0.7重量部、イオン交
換水100重量部、ドデシベンゼンスルホン酸ナトリウ
ム1.0重計部および−・ドデシルメルカプタン0.2
重険部の混合物をオートクレーブ中で80℃で6時間乳
化共重合させた後、苛性ソーダでP H6,0に調整し
、ラテックス固形分を部重量%に調整してSBRラテッ
クスを得た。 別に、スチレン52重量部、アクリル酸
t・ブチル45重量部、イタコン酸3 重i部、ドデ7
ルベンゼンスルポン酸l@計部、過硫酸力’) 15 
爪歇部および水110重に部の混合物を75℃で2時間
、85℃で3時間乳化重合して約48重量%のスチレン
−アクリル酸t・ブチル−イタコン酸共重合体の樹脂水
性エマルジョンを得た。
Example 1 33 parts by weight of butadiene, 65 parts by weight of methyleph, 2 parts by weight of acrylic acid, 0.7 parts by weight of sodium persulfate, 100 parts by weight of ion-exchanged water, 1.0 parts by weight of sodium dodecybenzenesulfonate, and -・Dodecyl mercaptan 0.2
After emulsion copolymerizing the mixture in the heavy part in an autoclave at 80° C. for 6 hours, the pH was adjusted to 6.0 with caustic soda, and the solid content of the latex was adjusted to % by weight to obtain SBR latex. Separately, 52 parts by weight of styrene, 45 parts by weight of t-butyl acrylate, 3 parts by weight of itaconic acid, 7 parts by weight of dode.
Rubenzenesulfonic acid l@meter, persulfuric acid power') 15
A mixture of the nail part and 110 parts by weight of water was emulsion polymerized at 75°C for 2 hours and at 85°C for 3 hours to obtain a resin aqueous emulsion of about 48% by weight of styrene-t-butyl acrylate-itaconic acid copolymer. Obtained.

上記三元共重合体の樹脂水性エマルジョン100重量部
に上記SBRラテックス100重量部、および加硫剤と
して住友化学■製メチロールメラミン樹脂気メラミンM
31F(商品名)5重量部、酸化チタン10重量部、カ
ーボンブラック0.05重量部を配合して最低造膜温度
が約18℃の水性分散液を調製した。 次いで、この水
性分散液を肉厚20+n+n、縦200 mm 、横2
001+II++のラワン板の力面上に肉厚が300ミ
クロンの塗膜が形成できるようにロールコータ−を用い
て塗布した後、温度20℃、湿度55RH%の恒温室で
24時間保存して乾燥し、塗膜をラワン板の全表面に形
成させ、このラワン板を130℃で1時間加熱してSB
Rラテックスの加硫を行なった。 そして、ラワン板上
に形成された塗膜の静摩擦係数(:r x s z −
0606−1982すべり試験で求めたすベシ角から換
算した値)は0.65 であることを確認した。
100 parts by weight of the aqueous resin emulsion of the above terpolymer, 100 parts by weight of the above SBR latex, and methylolmelamine resin gas Melamine M manufactured by Sumitomo Chemical ■ as a vulcanizing agent.
31F (trade name), 10 parts by weight of titanium oxide, and 0.05 parts by weight of carbon black were blended to prepare an aqueous dispersion having a minimum film forming temperature of about 18°C. Next, this aqueous dispersion was prepared into a mold with a wall thickness of 20+n+n, a length of 200 mm, and a width of 2
After applying the coating using a roll coater to form a coating film with a thickness of 300 microns on the force side of the lauan board of 001+II++, it was stored for 24 hours and dried in a constant temperature room at a temperature of 20°C and a humidity of 55RH%. , a coating film was formed on the entire surface of the lauan board, and the lauan board was heated at 130°C for 1 hour to form SB.
Vulcanization of R latex was performed. Then, the static friction coefficient of the coating film formed on the lauan board (: r x s z −
0606-1982 sliding test) was confirmed to be 0.65.

上記の如く、表面処理されたラワン板を試料片として、
耐候試験機内に300時間(屋外試験の1年分に相当)
および900時間(屋外試験の3年分に相当)保存した
後、この試料片を取り出して、外観(塗膜のひび割れ、
ピンホールの有無、ラワン板のそりの有無)、静摩擦係
数、耐落下衝撃性(試料片を高さ1mよりモルタル面上
に落下させた時の塗膜およびラワン板のひび割れの有無
)、耐候性試験後の吸水試験による重量増加率等を調べ
だ。 その結果は後記衣2と表3に本発明の他の実施例
および本発明に対する比較例のそれとイフ1せて示す。
As mentioned above, a surface-treated lauan plate was used as a sample piece,
300 hours in a weather test machine (equivalent to one year of outdoor testing)
After storage for 900 hours (equivalent to 3 years of outdoor testing), the specimen was taken out and the appearance (paint film cracks,
(presence or absence of pinholes, presence or absence of warpage of lauan board), static friction coefficient, drop impact resistance (presence or absence of cracks in the coating film and lauan board when a sample piece is dropped from a height of 1 m onto the mortar surface), weather resistance After the test, the weight increase rate, etc. was determined by the water absorption test. The results are shown in Table 3 below, together with those of other examples of the present invention and comparative examples for the present invention.

実施例■及び■と比較例1及び■ コノ・ラテックス、加硫剤、樹脂水性エマルジョンの種
類および量を下記表1のように変え、かつ、加硫温度と
時間を同表に示すように変える他は、実施例Iと同様に
実施して、塗膜を表面に有するラワン板を得、これを評
価した。
Examples ■ and ■ and Comparative Examples 1 and ■ The types and amounts of Kono latex, vulcanizing agent, and aqueous resin emulsion were changed as shown in Table 1 below, and the vulcanization temperature and time were changed as shown in the same table. The rest was carried out in the same manner as in Example I to obtain a lauan plate having a coating film on the surface, and this was evaluated.

なお、」−記表1において、へ、T S R0592”
 (商品名)は日本合成ゴム■製のSBRラブックス、
’ButakonML−507”(商品名)はIOI社
製のメシルメタクリレート(42重置火)−フタジエン
共重合体ラテックスであり、また、EVAエマルジョン
は酢酸ビニル(40重量%)−エブレン(60重量%)
共重合体にポリビニルアルコール5重量部を添加した樹
脂水性エマルジョン、Th、4−デコート T19U1
−1 〃(商品名)は日本ペイント■製の水性エマルジ
ョン塗料である。
In addition, in Table 1, TSR0592
(Product name) is SBR Lovex manufactured by Japan Synthetic Rubber.
'Butakon ML-507' (trade name) is a mesyl methacrylate (42-fold)-phtadiene copolymer latex manufactured by IOI, and the EVA emulsion is vinyl acetate (40% by weight)-Eblene (60% by weight).
Aqueous resin emulsion prepared by adding 5 parts by weight of polyvinyl alcohol to a copolymer, Th, 4-Decoat T19U1
-1 (Product name) is a water-based emulsion paint manufactured by Nippon Paint ■.

なお、表2及び表3に示した車酔増加率は、試別ハを2
5℃の水に24時間浸漬し、取り出した後の試別11の
Htt増加分を6分比で表わしたものである。
Note that the car sickness increase rates shown in Tables 2 and 3 are based on the trial
The increase in Htt of sample No. 11 after being immersed in water at 5° C. for 24 hours and taken out is expressed as a 6-minute ratio.

本発明は上記の如くであって、表2及び表3で明らかな
ように極めて優れた塗膜を水利表面に形成でき、水利の
耐久性を著しく向上できる利点がある1゜ 特πF出願人 三菱油化株式会社
The present invention is as described above, and as is clear from Tables 2 and 3, it has the advantage of being able to form an extremely excellent coating film on the surface of the irrigation system and significantly improving the durability of the irrigation system.Applicant: Mitsubishi Yuka Co., Ltd.

Claims (2)

【特許請求の範囲】[Claims] (1)  ゴムラテックスと加硫剤と樹脂水性エマルジ
ョンを含有する水性分散液を木材表面に塗布した後、乾
燥させ、次いで加熱して加硫反応を行なわせて木材表面
上に塗膜を形成させ、ることを特徴とする木材の表面処
理方法。
(1) After applying an aqueous dispersion containing rubber latex, a vulcanizing agent, and an aqueous resin emulsion to the wood surface, it is dried, and then heated to cause a vulcanization reaction to form a coating film on the wood surface. A method for surface treatment of wood, characterized by:
(2)水性分散液のゴムラテックスと樹脂水性エマルジ
ョンの固形分の重量比がV3〜hであることを特徴とす
る特許 材の表面処理方法。
(2) A method for surface treatment of a patented material, characterized in that the weight ratio of the solid content of the rubber latex in the aqueous dispersion and the solid content of the aqueous resin emulsion is V3 to h.
JP13576582A 1982-08-05 1982-08-05 Surface treating method for wood Pending JPS5926203A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13576582A JPS5926203A (en) 1982-08-05 1982-08-05 Surface treating method for wood

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13576582A JPS5926203A (en) 1982-08-05 1982-08-05 Surface treating method for wood

Publications (1)

Publication Number Publication Date
JPS5926203A true JPS5926203A (en) 1984-02-10

Family

ID=15159336

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13576582A Pending JPS5926203A (en) 1982-08-05 1982-08-05 Surface treating method for wood

Country Status (1)

Country Link
JP (1) JPS5926203A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0554262U (en) * 1991-12-20 1993-07-20 株式会社イノアックコーポレーション Tray for carrying goods

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0554262U (en) * 1991-12-20 1993-07-20 株式会社イノアックコーポレーション Tray for carrying goods

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