JPS5912982A - Adhesive composition - Google Patents

Adhesive composition

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Publication number
JPS5912982A
JPS5912982A JP12221182A JP12221182A JPS5912982A JP S5912982 A JPS5912982 A JP S5912982A JP 12221182 A JP12221182 A JP 12221182A JP 12221182 A JP12221182 A JP 12221182A JP S5912982 A JPS5912982 A JP S5912982A
Authority
JP
Japan
Prior art keywords
urea
component
formaldehyde
amount
added
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
JP12221182A
Other languages
Japanese (ja)
Inventor
Kiyoji Sugiura
杉浦 喜代治
Toshiaki Mutsutani
六谷 敏明
Masaru Odagiri
小田桐 勝
Hideaki Saito
英明 斉藤
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
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 Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP12221182A priority Critical patent/JPS5912982A/en
Publication of JPS5912982A publication Critical patent/JPS5912982A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

PURPOSE:The titled composition having improved storage stability, pot life of paste blended with an adhesive, initial bond strength after cold pressurizing, and bond strength resistant to warm water, obtained by blending an amino resin with specific amounts of polyacrylamide, polyvalent metallic compound, formaldehyde and urea. CONSTITUTION:(A) 100pts.wt. amino resin such as urea resin, urea-melamine co- condensation resin, etc. is blended with (B) 0.1-10pts.wt. nonionic polyacrylamide, (C) 0.1-5pts.wt. polyvalent metallic compound, preferably aluminum sulfate, etc., (D) formaldehyde (the preferable amount added is an amount equimolar with the component B when it is previously reacted with the component B and 1-10pts.wt. excess amount calculated as pure component D based on the component A when the component A is added in its use), and (E) urea (preferably amount is an amount to give a molar ratio of it to the component D added of 1.0-1.5), to give the desired composition. USE:Useful for preparing plywood, particle board, etc. with a low content of released formaldehyde.

Description

【発明の詳細な説明】 本発明は放出ホルムアルデヒド量の少い合板、パーチク
ルボードおよびハードボード等の製造に1吏用される接
着剤組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an adhesive composition for use in the production of plywood, particle board, hardboard, etc., which releases a small amount of formaldehyde.

近年、合板およびパーチクルボード等から放出されるホ
ルムアルデヒドの人体への影響が懸念され、日本農林規
格および日本工業規格の改正が行なわれ、合板およびパ
ーチクルボードより放出するホルムアルデヒド量が規制
されている。
In recent years, there has been concern about the effects of formaldehyde emitted from plywood, particle boards, etc. on the human body, and the Japanese Agricultural Standards and Japanese Industrial Standards have been revised to regulate the amount of formaldehyde emitted from plywood and particle boards.

合板およびパーチクルボードの製造には、尿素系化合物
、フェノール系化合物およびメラミンの少くとも1種と
ホルムアルデヒドとを主原料として製造される初期縮合
物が最も汎用されているシよ、合板およびパーチクルボ
ルドより放出されるホルムアルデヒド量を規制するため
には、尿素系化合物、フェノール系化合物、またはメラ
ミンに対するホルムアルデヒドのモル比を15以下にす
る必要があるが、これでは得られるアミン樹脂の貯蔵安
定性が悪く、また合板製造時における冷圧後の初期接着
力が小さく、得られる合板およびパーチクルボードの耐
温水接着力も低い。
In the production of plywood and particle board, the most commonly used initial condensate is a urea compound, a phenol compound, and at least one of melamine, and formaldehyde. In order to control the amount of formaldehyde produced, it is necessary to keep the molar ratio of formaldehyde to urea compounds, phenolic compounds, or melamine to 15 or less, but this results in poor storage stability of the resulting amine resin, and The initial adhesive strength after cold pressing during plywood production is low, and the hot water resistant adhesive strength of the resulting plywood and particle board is also low.

上記した従来法の欠点を改良するため、特公昭36−7
537および特公昭5’5−22519にはポリビニル
アルコール、ポリアクリルアマイドおよびポリ耐酸ビニ
ールのようなビニール系高分子化合物を添加し、貯蔵安
定性および初期接着力 を改善する/ 方法が開示されている。
In order to improve the above-mentioned drawbacks of the conventional method,
537 and Japanese Patent Publication No. 5'5-22519 disclose a method for improving storage stability and initial adhesive strength by adding vinyl polymer compounds such as polyvinyl alcohol, polyacrylamide, and polyacid-resistant vinyl. .

しかしながら、上記した従来技術では、熱可塑性のビ・
ニール系高分子化合物を添加するためN初期接着力は改
善されるものの耐温水接着力は低下し、又、高分子化合
物を添加するため、得られる接着剤が増粘し貯蔵安定性
が悪化したり、接着剤配合糊の可使時間が短かく逆に貯
蔵安定性を悪化させないためにはビニール系高分子化合
物は微量しか添加できず、結局、初期接着力の向上は望
めなかった。
However, in the above-mentioned conventional technology, thermoplastic plastic
Although the initial adhesion of N is improved due to the addition of a Neil-based polymer compound, the hot water resistant adhesive strength is reduced.Additionally, the addition of a polymer compound increases the viscosity of the resulting adhesive and deteriorates its storage stability. In addition, the pot life of the adhesive-containing paste is short, and in order to avoid deteriorating the storage stability, only a small amount of the vinyl-based polymer compound can be added, and as a result, no improvement in the initial adhesive strength can be expected.

本発明は、貯蔵安定性の改良および、接着剤配合糊の可
使時間冷圧後の初期接着力並びに耐温水接着力の増大を
目的とするものである。
The object of the present invention is to improve the storage stability and to increase the initial adhesive strength and hot water resistant adhesive strength after cold pressing during the pot life of the adhesive-containing paste.

本発明者らは、これ等の課題を達成するために鋭意研究
の結果、アミン樹脂に特定緻のポリメチロールアクリル
アマイドおよび多価金属化合物を加えることにより、初
期接着力、および耐温水接着力の増大をもたらし、接着
剤組成物の貯蔵安定性が良好で接着剤配合糊の可使時間
が延長され、又、高含水率単板およびチップ使用時のパ
ンク防止効果が大きいことを見出して本発明を完成した
As a result of intensive research to achieve these goals, the present inventors have found that by adding a specific amount of polymethylol acrylamide and a polyvalent metal compound to the amine resin, the initial adhesive strength and hot water resistant adhesive strength can be improved. The present invention was based on the discovery that the storage stability of the adhesive composition is good, the pot life of the adhesive compounded paste is extended, and the puncture prevention effect is large when using high moisture content veneers and chips. completed.

即ち、本発明は、アミノ樹脂100重量部に、a)、0
1〜10重量部のポリアクリルアマイド、b)01〜5
重量部の多価金属化合物、C)ホルムアルデヒドおよび
d)尿素を添加したことを特徴とする接着剤組成物であ
る。
That is, in the present invention, a), 0
1-10 parts by weight of polyacrylamide, b) 01-5
An adhesive composition characterized in that parts by weight of a polyvalent metal compound, C) formaldehyde, and d) urea are added.

本発明において使用されるアミン樹脂としては、尿素樹
脂、メラミン樹脂、ベンゾグアナミン樹脂、アセトグア
ナミン樹脂、チオ尿素樹脂またはこれらの混合物、もし
くは共縮合樹脂が挙げられ、捷だそれら人の樹脂とフェ
ノール樹脂、レゾルシノール樹脂、トルエン樹脂および
キシレン樹脂との共縮合樹脂が含まれる。而して上記し
た樹脂に、ポリビニールアルコールまたはセルロース系
の増粘剤を添加することは差支えない。
Amine resins used in the present invention include urea resins, melamine resins, benzoguanamine resins, acetoguanamine resins, thiourea resins, mixtures thereof, or co-condensation resins, and these resins and phenolic resins may be used. Includes co-condensation resins with resorcinol resins, toluene resins and xylene resins. There is no problem in adding polyvinyl alcohol or cellulose-based thickener to the above-mentioned resin.

本発明においては、接着剤使用時に、アミン樹脂にポリ
アクリルアマイドとホルムアルデヒド水を混合又は反応
させ、ついでアミノ樹脂に添加して本発明の接着剤組成
物として使用しても良い。
In the present invention, when using the adhesive, polyacrylamide and formaldehyde water may be mixed or reacted with the amine resin, and then added to the amino resin to be used as the adhesive composition of the present invention.

本発明において使用されるポリアクリルアマイドとして
は、ノニオン性のポリアクリルアマイド、カチオン性の
マンニッヒ化ポリアクリルアマイド、ビニルラクタム−
アクリルアマイド共重合体、アニオン性のアクリル酸ノ
ーグーアクリルアマイド共重合体等をあげることができ
る。
Examples of the polyacrylamide used in the present invention include nonionic polyacrylamide, cationic Mannich polyacrylamide, and vinyllactam polyacrylamide.
Examples include acrylamide copolymers, anionic acrylic acid no-goo acrylamide copolymers, and the like.

本発明の接着剤組成物におけるポリアクリルアマイドの
添加量:は、アミン樹脂100重量部に対し、01〜1
0重隈部、好ましくは01〜5重量部の範r、fllで
添加することが必要である。添加量が0,1重置部より
低い場合は、初期接着力の効果は得られず、又10重量
部より多い場合はえられる接着剤組成物の貯蔵安定性が
低下する。
The amount of polyacrylamide added in the adhesive composition of the present invention is 01 to 1 with respect to 100 parts by weight of the amine resin.
It is necessary to add 0 parts by weight, preferably in the range of 01 to 5 parts by weight. If the amount added is less than 0.1 parts by weight, no effect on initial adhesive strength will be obtained, and if it is more than 10 parts by weight, the storage stability of the resulting adhesive composition will be reduced.

ホルムアルデヒドの添加量は、前記のようにポリアクリ
ルアマイドと反応させておくためには、ポリアクリルア
マイドと当量で良いが、使用時にアミン系樹脂に加える
場合および単にアクリルアマイドとホルムアルデヒドと
を混合する場合は、当−以」二1.すなわちアミン樹脂
に対してホルムアル。
The amount of formaldehyde added may be equivalent to the amount of polyacrylamide in order to react with the polyacrylamide as described above, but when adding it to the amine resin at the time of use or when simply mixing acrylamide and formaldehyde. 21. i.e. formal versus amine resin.

テヒド純分として通常1〜10重量部過剰に添加するこ
とが心安である。上記したホルムアルデヒドの添加によ
り、合板およどびパーチクルホード等から放出されるホ
ルムアルデヒドの針を減らすため尿素を加えることが必
要である。尿素の添加量は上記したホルムアルデヒドの
添加量に対してモル比で1.0〜15に調整することが
望ましい。
It is safe to add usually 1 to 10 parts by weight of pure tehyde. Due to the addition of formaldehyde mentioned above, it is necessary to add urea to reduce the formaldehyde needles emitted from plywood and particle hoards, etc. The amount of urea added is desirably adjusted to a molar ratio of 1.0 to 15 with respect to the amount of formaldehyde mentioned above.

本発明における多価金属化合物とは、周期律表第2属か
ら第8属の金属および遷移金属のうち、2価以上の多価
金属の酸化物及び塩であり、前者としてはたとえばカル
シウム、マグネシウム、亜鉛、バリウム、カドミウム、
鉛、銅、アルミニウム、鉄、ジルコニウムおよびクロム
などがあげられ、またこれらの酸化物の構成成分となっ
ているベントナイト、クレー、タルク〆もこれらに準す
るものとしてあげられる。
The polyvalent metal compounds in the present invention are oxides and salts of polyvalent metals of divalent or higher valence among metals from Groups 2 to 8 of the periodic table and transition metals, and examples of the former include calcium, magnesium, etc. , zinc, barium, cadmium,
Examples include lead, copper, aluminum, iron, zirconium, and chromium, as well as bentonite, clay, and talc, which are constituent components of these oxides.

また多価金属塩としては、上記多価金属の炭酸塩、硫酸
塩、硝酸塩、酢酸塩、塩化物およびケイ酸塩などの塩が
あげられる。
Examples of polyvalent metal salts include carbonates, sulfates, nitrates, acetates, chlorides, and silicates of the above-mentioned polyvalent metals.

これらの中では、たとえば炭酸ジルコニウム、硫酸アル
ミニウム、硝酸クロム、酢酸ジルコニウム、塩化アルミ
ニウム、塩化第1鉄および塩化第2鉄等の酸性塩の利用
が望ましい。而してこれらの金属塩、酸化物は、このう
ちの1種のみを用いてもよいし、また2種以上を同時に
用いてもよい。
Among these, it is desirable to use acidic salts such as zirconium carbonate, aluminum sulfate, chromium nitrate, zirconium acetate, aluminum chloride, ferrous chloride, and ferric chloride. These metal salts and oxides may be used alone or in combination of two or more.

これらの多価金属化合物の添加量は、アミン樹脂性は悪
く、高含水率単板使用時のパンク防止効果がとぼしく、
又、5重量部より多いと初期接着力及び耐水接着力が低
下する。
The amount of these polyvalent metal compounds added results in poor amine resin properties and poor puncture prevention effect when using high moisture content veneer.
Furthermore, if the amount is more than 5 parts by weight, the initial adhesive strength and water-resistant adhesive strength will decrease.

本発明の実施においては、従来より用いられている増量
剤としての小麦粉の他に、大麦粉、米粉、木粉、タルク
、クレー等を用いたシ、仮接着向上を目的とするポリビ
ニールアルコール等の化合物および従来高含水率単板対
策として用いられている血粉、大豆粉、とうもろこし粉
等を併用することはさしつかえない。
In carrying out the present invention, in addition to wheat flour as a bulking agent conventionally used, barley flour, rice flour, wood flour, talc, clay, etc. may be used, and polyvinyl alcohol for the purpose of improving temporary adhesion may be used. It is permissible to use the compound in combination with blood meal, soybean meal, corn meal, etc., which have been conventionally used as a countermeasure for high moisture content veneers.

本発明の方法によれば、接着剤の貯蔵安定性は、高分子
化合物を添加しであるにもかかわらず良好であり、接着
剤組成物の可使時間も充分長く、実用上問題はない。
According to the method of the present invention, the storage stability of the adhesive is good despite the addition of a polymer compound, and the pot life of the adhesive composition is sufficiently long, so that there are no practical problems.

またポリアクリルアマイドの粘着力により、合板製造時
の初期接着力が高く、冷圧圧締時間が短かくてすみ、又
、20〜25重量%のような高含水率単板を使用するこ
とも可能である。
In addition, due to the adhesive strength of polyacrylamide, the initial adhesive strength during plywood production is high, and the cold pressing time is short, and it is also possible to use high moisture content veneer such as 20 to 25% by weight. It is.

本発明の方法によれば、ポリアクリルアマイドのような
熱可塑性樹脂を使用しているにもがかわらず、ホルムア
ルデヒドと多価金属化合物を仲立ちとしてアミン樹脂と
架橋するため、耐湯水接着力が低下せず、接着力が安定
し且つ放出ホルムアルデヒドの少い合板、パーチクルボ
ードおよびハードボードを製造することが可能となり、
まだ高含水率の単板およびチップを使用した時の合板、
パーチクルボード並びにハードボードのパンク防止がは
かれる。
According to the method of the present invention, although a thermoplastic resin such as polyacrylamide is used, it is crosslinked with an amine resin using formaldehyde and a polyvalent metal compound as an intermediary, resulting in a decrease in hot water resistant adhesive strength. It is now possible to produce plywood, particle board, and hardboard that have stable adhesive strength and emit less formaldehyde.
Plywood when using veneers and chips that still have high moisture content,
Particle board and hardboard can be prevented from punctures.

て実用上の価値は高い。It has high practical value.

次に、実施例および比較例により、本発明を具体的に説
明する。後述する文中におけるチは木破率に関するチ以
外は重量%を示し部は重量部を示す。
Next, the present invention will be specifically explained using Examples and Comparative Examples. In the following text, except for those related to the percentage of wood breakage, "chi" indicates weight %, and "part" indicates parts by weight.

実施例1 尿素樹脂(三井東圧(割裂、ニーロイドU−701、商
品名)100部にあらかじめポリアクリルアマイド(三
井すイpナミツド■製アコーフロックN−10部8商品
名)1部と67%ホルムアルデヒド溶′ti、3部、尿
素2部、硫酸アルミニウム6部を加え接着剤組成物をえ
た。それにさらに、小麦粉15部、水20部、塩化アン
モニウム1部を加え、撹拌混合して、合板用接着剤配合
糊を得、該配合糊を使用して下記接着条件にて合板を製
造した。
Example 1 100 parts of urea resin (Mitsui Toatsu (Warisaki, Nyroid U-701, trade name)) was preliminarily mixed with 1 part of polyacrylamide (Mitsui Suipunamitsu ■, Acofflock N-10 part 8 trade name) and 67%. An adhesive composition was obtained by adding 3 parts of formaldehyde solution, 2 parts of urea, and 6 parts of aluminum sulfate.Furthermore, 15 parts of wheat flour, 20 parts of water, and 1 part of ammonium chloride were added and mixed by stirring. An adhesive compounded paste was obtained, and plywood was manufactured using the compounded glue under the following bonding conditions.

接着剤組成物、配合糊、合板の性能を表1に示した。Table 1 shows the performance of the adhesive composition, blended paste, and plywood.

一接着条件一 単板構成  0.6+13+o6”7mの各厚みからな
るラワン単板の3層構成 単板含水率 原板、中板共7〜10% 塗伺量   25 fi’ / 900 cni堆積時
間  20分 冷圧条件 ’ 12 Kg/Cwt、60分熱圧条件 
 1o kg / cnl、120℃、50秒/枚舛初
期接着力は冷圧解圧20分後の状態をみた。
- Adhesion conditions - Veneer composition: 3-layer composition of lauan veneer with each thickness of 0.6 + 13 + O6” 7m Veneer moisture content: 7-10% for both original and intermediate boards Coverage: 25 fi' / 900 cni Deposition time: 20 minutes Cold pressure condition '12 Kg/Cwt, 60 minutes hot pressure condition
10 kg/cnl, 120°C, 50 seconds/sheet Initial adhesion strength was measured 20 minutes after cold decompression.

実施例2 尿素樹脂(三井東圧■製、ニーロイドU −701、商
品名)100部にあらかじめポリアクリルアマイド(三
井すイアナミツド■製、アコ−フロレフN−1008、
商品名)2部と、67%ホルムアルデヒド水溶液5部、
尿素6部、塩化アルミニウム2部、水10部を加熱混合
したものを加え、さらに□小麦粉20部、水11部、塩
化アンモニウム1部を加え、撹拌混合して合板用接着剤
配合糊をえた。
Example 2 100 parts of urea resin (manufactured by Mitsui Toatsu ■, Niroid U-701, trade name) was preliminarily added with polyacrylamide (manufactured by Mitsui Toatsu ■, Aco-Floref N-1008,
Product name) 2 parts, 5 parts of 67% formaldehyde aqueous solution,
A heated mixture of 6 parts of urea, 2 parts of aluminum chloride, and 10 parts of water was added, and further 20 parts of wheat flour, 11 parts of water, and 1 part of ammonium chloride were added and mixed with stirring to obtain a paste containing an adhesive for plywood.

単板含水率を16〜20%にした以外は実施例1と同一
の接着条件で合板を製造し、その性能を表1に示した。
Plywood was manufactured under the same bonding conditions as in Example 1, except that the moisture content of the veneer was set to 16 to 20%, and its performance is shown in Table 1.

実施例5 尿素樹脂の代わシに尿素−メライン共縮合樹脂(三井東
圧(割裂、ニーロイドU −350、商品名)を、又1
.塩化アルミニウムの代わりに塩化第2鉄曾用いて実施
例2と同一の条件で合板を製造し、その性能を表1に示
した。
Example 5 In place of the urea resin, a urea-melain cocondensation resin (Mitsui Toatsu (Warisaki, Niroid U-350, trade name)) was used.
.. Plywood was manufactured under the same conditions as in Example 2 using ferric chloride instead of aluminum chloride, and its performance is shown in Table 1.

実施例4〜7 アミノ樹脂、ポリアクリルアマイド、多価金属化合物、
37係ホルムアルデヒド水溶液、尿素を表1に示す割合
で撹打混合し、合板用接着剤配合糊をえた。実施例1と
同一の接着条件で合板を製造し、その性能を表1に示し
た。
Examples 4 to 7 Amino resin, polyacrylamide, polyvalent metal compound,
A formaldehyde aqueous solution of Section 37 and urea were stirred and mixed in the proportions shown in Table 1 to obtain a paste containing an adhesive for plywood. Plywood was manufactured under the same bonding conditions as in Example 1, and its performance is shown in Table 1.

比較例1〜5 アミン樹脂、ポリアクリルアマイド、多価金属化合物、
67%ホルムアルデヒド水溶液および尿素を表2に示す
割合で撹拌混合し、合板用接着剤配合糊をえた。更に実
施例1と同一の接着条件で合板を製造し、その性能を表
2に示した。
Comparative Examples 1 to 5 Amine resin, polyacrylamide, polyvalent metal compound,
A 67% formaldehyde aqueous solution and urea were stirred and mixed in the proportions shown in Table 2 to obtain a paste containing an adhesive for plywood. Furthermore, plywood was manufactured under the same bonding conditions as in Example 1, and its performance is shown in Table 2.

参考例1〜4 アミン樹脂、ポリアクリルアマイド、多価金属化合物、
67%ホルムアルデヒド水溶液および尿素を表6に示す
割合で撹拌混合し、合板用接着剤配合糊をえた。更に、
実施例1と同一の接着条件で合板を製造し、その性能を
表6に示した。
Reference Examples 1 to 4 Amine resin, polyacrylamide, polyvalent metal compound,
A 67% formaldehyde aqueous solution and urea were stirred and mixed in the proportions shown in Table 6 to obtain a paste containing an adhesive for plywood. Furthermore,
Plywood was manufactured under the same bonding conditions as in Example 1, and its performance is shown in Table 6.

〔註〕[Note]

≠1) U P :尿素樹脂、UMF:尿素・メラミン
樹脂、MPF:メラミン、フェノール樹脂H2)PAM
:ポリアクリルアマイド −X3)三井妾イアナミッド■製 アコ−フロック  
0−2535 ¥4)実施例6,4以外は、日本農林規格温冷水浸せき
試験による。
≠1) UP: urea resin, UMF: urea/melamine resin, MPF: melamine, phenolic resin H2) PAM
: Polyacrylamide -
0-2535 ¥4) Except for Examples 6 and 4, the test was conducted according to the Japanese Agricultural Standards hot and cold water immersion test.

実施例6,4は、日本農林規格煮沸くり返し試験による
Examples 6 and 4 were based on the repeated boiling test according to the Japanese Agricultural Standards.

XS)三井サイアナミツド側製 アコ−フロック  A
−110
XS) Mitsui Cyanamitsu Aco-Flock A
-110

Claims (1)

【特許請求の範囲】 旬 アミノ樹脂100重量部に、a)01〜10重量部
のポリアクリルアマイド、b)01〜5重量部の多価金
属化合物、c)ホルムアルデヒド及びd)尿素を添加し
たことを特徴とする接着剤組成物。 2)多価金属化合物が酸性塩である特許請求の範囲第1
項記載の接着剤組成物。
[Scope of Claims] Shun To 100 parts by weight of amino resin, a) 01 to 10 parts by weight of polyacrylamide, b) 01 to 5 parts by weight of a polyvalent metal compound, c) formaldehyde, and d) urea are added. An adhesive composition characterized by: 2) Claim 1 in which the polyvalent metal compound is an acid salt
The adhesive composition described in .
JP12221182A 1982-07-15 1982-07-15 Adhesive composition Pending JPS5912982A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12221182A JPS5912982A (en) 1982-07-15 1982-07-15 Adhesive composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12221182A JPS5912982A (en) 1982-07-15 1982-07-15 Adhesive composition

Publications (1)

Publication Number Publication Date
JPS5912982A true JPS5912982A (en) 1984-01-23

Family

ID=14830295

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12221182A Pending JPS5912982A (en) 1982-07-15 1982-07-15 Adhesive composition

Country Status (1)

Country Link
JP (1) JPS5912982A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6489392B1 (en) * 1998-03-09 2002-12-03 Dynea Chemicals Oy Foamed resin adhesive and the use thereof of glueing wood based panels and boards

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6489392B1 (en) * 1998-03-09 2002-12-03 Dynea Chemicals Oy Foamed resin adhesive and the use thereof of glueing wood based panels and boards

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