JPH07126596A - Adhesive for wood materials - Google Patents

Adhesive for wood materials

Info

Publication number
JPH07126596A
JPH07126596A JP27153793A JP27153793A JPH07126596A JP H07126596 A JPH07126596 A JP H07126596A JP 27153793 A JP27153793 A JP 27153793A JP 27153793 A JP27153793 A JP 27153793A JP H07126596 A JPH07126596 A JP H07126596A
Authority
JP
Japan
Prior art keywords
formaldehyde
adhesive
resin
aminoplast resin
amount
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
JP27153793A
Other languages
Japanese (ja)
Inventor
Gakushi Kageyama
学史 蔭山
Kyoshi Kiritooshi
京士 切通
Kazuaki Yamada
和明 山田
Hiroyuki Kaigaishi
博之 貝ケ石
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 JP27153793A priority Critical patent/JPH07126596A/en
Publication of JPH07126596A publication Critical patent/JPH07126596A/en
Pending legal-status Critical Current

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  • Adhesives Or Adhesive Processes (AREA)

Abstract

PURPOSE:To obtain an adhesive for a wooden material which can suppress the released of formaldehyde, can maintain rapid curability, and can keep water resistance of the adhesiveness under the ordinary condition for using an aminoplast resin. CONSTITUTION:This adhesive is prepd. by adding 0.2-20 pts.wt. glyoxal to 100 pts.wt. water-soluble aminoplast resin wherein formaldehyde is a main component. By using this adhesive, a wooden product wherein, even when the content of free formaldehyde in the water-soluble aminoplast resin is reduced to at most 1wt.%, it is unnecessary to prolong the curing time or to sacrifice the productivity, and the physical properties and water resistance can be kept and the amt. of the released aldehyde is small can be obtd.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は合板、パーチクルボー
ド、MDF、等の木質材料の製造に使用する接着剤に関
するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an adhesive used for manufacturing wood materials such as plywood, particle board and MDF.

【0002】[0002]

【従来の技術】従来、木質材用接着剤としては水溶性尿
素樹脂、メラミン樹脂、フェノール樹脂等の水溶性アミ
ノプラスト樹脂が広く用いられている。しかし、これら
の樹脂中には遊離ホルムアルデヒドが含有されており、
硬化を早めるために更にホルムアルデヒドを添加するこ
ともある。従って使用時のホルムアルデヒド臭気が強
く、又製品木質材中にも、遊離ホルムアルデヒドが残留
するため、ホルムアルデヒドガスが放出され、家屋内の
板材、家具等に用いた場合ホルムアルデヒド臭気が問題
となり、人体への衛生上の見地からも思わしくない。
2. Description of the Related Art Conventionally, water-soluble aminoplast resins such as water-soluble urea resins, melamine resins and phenol resins have been widely used as adhesives for wood materials. However, these resins contain free formaldehyde,
Further formaldehyde may be added to accelerate the curing. Therefore, the formaldehyde odor during use is strong, and free formaldehyde remains in the wood material of the product, so formaldehyde gas is released, and when it is used for indoor board materials, furniture, etc., the formaldehyde odor becomes a problem, From a hygiene standpoint, it doesn't look good.

【0003】しかしながら、使用時のホルムアルデヒド
臭気や製品中の遊離ホルムアルデヒドを低減するには、
接着剤中の残存ホルムアルデヒドの量を低減させること
が必要であるが、残存ホルムアルデヒドを低減する為に
はアミノプラスト樹脂合成時にアミノ基に対するホルム
アルデヒド量を少なくしたり、尿素、メラミン各種アミ
ン等のホルムアルデヒド捕捉剤をアミノプラスト樹脂に
配合したりする方法をとることになる。
However, in order to reduce formaldehyde odor during use and free formaldehyde in products,
It is necessary to reduce the amount of residual formaldehyde in the adhesive, but in order to reduce the amount of residual formaldehyde, the amount of formaldehyde with respect to amino groups during aminoplast resin synthesis should be reduced, and formaldehyde such as urea and melamine amine should be captured. The method is to mix the agent with the aminoplast resin.

【0004】[0004]

【発明が解決しようとする課題】しかし、かかる手段に
よるアミノプラスト樹脂を使用して合板、パーチクルボ
ード、MDFを製造した場合、樹脂の硬化時間が大幅に
遅れると同時に、硬化した製品は接着強度が低く、用途
が制限されてしまう。したがって従来のアミノプラスト
樹脂の硬化速度を落とすことなく、接着耐水性能も維持
して、かつ、ホルムアルデヒド臭気のない木質材用接着
剤が求められてきた。
However, when plywood, particle board and MDF are produced by using the aminoplast resin by such means, the curing time of the resin is significantly delayed and the cured product has a low adhesive strength. , The use is limited. Therefore, there has been a demand for an adhesive for wood materials which does not reduce the curing speed of the conventional aminoplast resin, maintains the adhesive water resistance, and has no formaldehyde odor.

【0005】[0005]

【課題を解決するための手段】本発明者らは上記問題点
につき鋭意検討を行った結果、アミノプラスト樹脂の通
常使用条件下で放出ホルムアルデヒドを少なく抑え、か
つ生産性を落とさぬよう速硬化特性を維持し、接着耐水
性能も維持向上出来る木質材用接着剤を得ることが出来
た。
Means for Solving the Problems As a result of intensive studies on the above problems, the present inventors have found that the formaldehyde released under the normal use conditions of aminoplast resin is small, and the rapid curing property is maintained so as not to reduce the productivity. It was possible to obtain an adhesive for wood materials that maintains the above-mentioned properties and maintains and improves the adhesive water resistance.

【0006】即ち、本発明の木質材用接着剤はホルムア
ルデヒドを主剤とする水溶性アミノプラスト樹脂100
重量部に対して、グリオキザールを0.2〜20重量部
添加したことを特徴とするものである。従来において
は、硬化時間短縮のためアミノプラスト樹脂にアンモニ
ウム塩や強酸硬化剤を通常用いる以上に用いると、残存
ホルムアルデヒドが1.0wt%以上のアミノプラスト
樹脂に於いてはゲルタイムの短縮効果は大きいが放出ホ
ルムアルデヒド量の低減効果はなく、さらに成形前にプ
レゲルのトラブルも有り得た。
That is, the adhesive for wood materials of the present invention is a water-soluble aminoplast resin 100 containing formaldehyde as a main component.
It is characterized in that 0.2 to 20 parts by weight of glyoxal is added to parts by weight. Conventionally, if an ammonium salt or a strong acid curing agent is used in the aminoplast resin in order to shorten the curing time more than usual, the effect of shortening the gel time is great in the aminoplast resin having residual formaldehyde of 1.0 wt% or more. There was no effect of reducing the amount of formaldehyde released, and there could have been problems with the pregel before molding.

【0007】また残存ホルムアルデヒド量が1.0wt
%以下、特に0.5wt%以下になると、アルデヒド臭
を減少させることは出来るが、アンモニウム塩や強酸硬
化剤を通常以上用いても大幅な硬化短縮効果がないと同
時に、接着耐水性も悪くなるので、残存ホルムアルデヒ
ドを低減させることが難しく、従って放出ホルムアルデ
ヒドも期待するほど低減できない。ところが、グリオキ
ザールを樹脂に添加してやると、硬化剤の添加量を多く
することなく通常硬化剤量で速硬化になり、かつ、硬化
剤の添加量も少ないので成形前のプレゲルもない。更に
残留ホルムアルデヒド1.0wt%以下の樹脂にしても
硬化時間を延長する必要無く、生産性を犠牲にせずにす
み物性、耐水性を保持し、かつ、放出ホルムアルデヒド
量の少ない合板、パーチクルボード等の木質製品を得る
ことが出来る。
The residual formaldehyde content is 1.0 wt.
% Or less, especially 0.5 wt% or less, it is possible to reduce the aldehyde odor, but even if an ammonium salt or a strong acid curing agent is used more than usual, there is no significant effect of shortening the curing and, at the same time, the adhesive water resistance deteriorates. Therefore, it is difficult to reduce the residual formaldehyde, and therefore the emitted formaldehyde cannot be reduced as expected. However, when glyoxal is added to the resin, the amount of the curing agent does not increase, and the curing agent usually cures rapidly with the amount of the curing agent, and since the amount of the curing agent added is small, there is no pregel before molding. Further, even if the residual formaldehyde is 1.0 wt% or less, it is not necessary to extend the curing time, and the wood properties such as plywood and particle board that retain the physical properties and water resistance without sacrificing the productivity and emit a small amount of formaldehyde. You can get the product.

【0008】本発明の木質材用接着剤において、グリオ
キザールの添加量を変えて配合した尿素樹脂の硬化時間
及び合板にしたときの接着強度、放出ホルムアルデヒド
及びパーチクルボードにしたときの放出ホルムアルデヒ
ド、曲げ強度、耐水性につき、従来の尿素樹脂、低臭気
尿素樹脂との比較をしてみると、尿素樹脂は汎用タイプ
に於いてはグリオキザールの添加量に伴い硬化時間の著
しい短縮効果がみられる。一方従来の低臭気尿素樹脂例
えば残存ホルムアルデヒド0.48%、0.25%のも
のを各々調べると、元の樹脂中の残存ホルムアルデヒド
量が少なくなると硬化時間の伸び傾向が著しく、生産性
が落ちるだけでなく、合板にしたときの強度、耐水性の
低下が著しい。
In the adhesive for wood materials of the present invention, the curing time of the urea resin compounded by changing the addition amount of glyoxal, the adhesive strength when formed into plywood, the released formaldehyde and the released formaldehyde when formed into a particle board, the bending strength, Regarding the water resistance, when comparing the conventional urea resin and the low-odor urea resin, the urea resin in the general-purpose type shows a remarkable shortening effect of the curing time with the addition amount of glyoxal. On the other hand, conventional low odor urea resins such as residual formaldehyde of 0.48% and 0.25% were examined, respectively. When the amount of residual formaldehyde in the original resin was reduced, the curing time tended to increase remarkably and the productivity was reduced. Not only that, the strength and water resistance of plywood are significantly reduced.

【0009】然るにグリオキザールを添加または一部反
応させることにより硬化時間の短縮効果が大きく、生産
性の向上になると同時に合板の残存ホルムアルデヒド量
を低減させて、放出ホルムアルデヒド量を低く維持しつ
つ強度、耐水性が著しく改善できる。この傾向はパーチ
クルボード、MDFを成形した場合にも同じである。グ
リオキザールの添加量は0.2重量部より低いと硬化時
間短縮効果、曲げ強度発現が弱く、20重量部以上は添
加しても硬化時間短縮効果、接着強度発現効果が飽和し
コスト高で使用しにくい。
However, by adding or partially reacting glyoxal, the curing time is greatly shortened and the productivity is improved. At the same time, the amount of residual formaldehyde in the plywood is reduced and the amount of formaldehyde released is kept low, while the strength and water resistance are kept low. Remarkably improved in sex. This tendency is the same when molding a particle board or MDF. If the addition amount of Glyoxal is less than 0.2 parts by weight, the curing time shortening effect and the flexural strength expression are weak, and if 20 parts by weight or more, the curing time shortening effect and the adhesive strength expression effect are saturated and the cost is high. Hateful.

【0010】本発明に於ける水溶性アミノプラスト樹脂
としては尿素樹脂、尿素・メラミン共縮合樹脂、尿素樹
脂、メラミン樹脂の混合体のみでなく、フェノール樹脂
を配合して使用することもできる。配合量は前記アミノ
プラスト樹脂100部に対し30部まで可能である。こ
れらアミノプラスト樹脂を木質材用接着剤として用いる
場合、通常用いる充填剤や増量剤を配合して用いること
もできる。充填剤や増量剤としては、小麦粉、米粉、大
麦粉、脱脂大豆粉、脱脂とうもろこし粉、こんにゃく粉
等の各種穀類粉末、木粉、タルク、クレー等の無機粉末
等一種または二種以上を用いることが出来る。
As the water-soluble aminoplast resin in the present invention, not only a urea resin, a urea / melamine co-condensation resin, a urea resin and a melamine resin mixture, but also a phenol resin may be blended and used. The compounding amount can be up to 30 parts with respect to 100 parts of the aminoplast resin. When these aminoplast resins are used as an adhesive for wood materials, it is also possible to mix and use fillers and extenders that are usually used. As the filler and extender, wheat flour, rice flour, barley flour, defatted soybean flour, defatted corn flour, various cereal powders such as konjac flour, wood flour, talc, use of one or more inorganic powders such as clay, etc. Can be done.

【0011】アミノプラスト樹脂の硬化剤としては、通
常公知な硬化剤を用いることが出来る。硬化剤としては
塩化アンモニウム等のアンモニウム塩、塩酸、酢酸、パ
ラトルエンスルホン酸、硫酸アルミニゥム、塩化アルミ
ニウムがあげられる。
As the curing agent for the aminoplast resin, a generally known curing agent can be used. Examples of the curing agent include ammonium salts such as ammonium chloride, hydrochloric acid, acetic acid, paratoluenesulfonic acid, aluminum sulfate, and aluminum chloride.

【0012】[0012]

【実施例】以下実施例により本発明を説明する。なお実
施例中の全ての部は、重量部である。また、評価試験法
は表1の方法による。
The present invention will be described with reference to the following examples. All parts in the examples are parts by weight. The evaluation test method is based on the method shown in Table 1.

【0013】[0013]

【表1】 [Table 1]

【0014】実施例1、2、3、7、8、及び比較例
4、5 所定量の尿素の一部、および37%ホルマリンの所定量
を仕込みアルカリ性にて加熱溶解し、一次反応を90℃
で30分間実施した後、酸性下にて80℃で尿素の残量
を遂時仕込み4時間反応させる。中和冷却後、所定量の
グリオキザールを添加し中和後製品とする。グリオキザ
ール添加前の樹脂中残存ホルムアルデヒド量を測定す
る。各々の樹脂で試験法Aにより100℃のゲルタイム
タイムを測定する。つぎに試験法Bにて配合糊を作り合
板を作成し、合板の接着力、放出ホルムアルデヒド量を
測定する。結果を表2に示す。
Examples 1, 2, 3, 7, 8 and Comparative Examples 4, 5 A predetermined amount of a portion of urea and a predetermined amount of 37% formalin were charged and dissolved by heating under alkaline conditions, and the primary reaction was carried out at 90 ° C.
After carrying out the reaction for 30 minutes at 80 ° C. under acidic condition, the remaining amount of urea is charged at room temperature and the reaction is carried out for 4 hours. After cooling by neutralization, a predetermined amount of glyoxal is added to neutralize the product. Measure the amount of formaldehyde remaining in the resin before adding glyoxal. The gel time time at 100 ° C. is measured according to test method A for each resin. Next, a compounding paste is prepared by Test Method B to prepare plywood, and the adhesive strength of the plywood and the amount of formaldehyde released are measured. The results are shown in Table 2.

【0015】実施例4、5、6 実施例1〜3に対応して同じく尿素、37%ホルマリン
を仕込みアルカリ性にて所定量加熱溶解し、一次反応を
90℃で30分実施後、酸性下にて80℃で尿素の所定
量を遂時仕込み、4時間反応させる。冷却時60℃にて
実施例1〜3に対応した所定量のグリオキザールを添加
30分放置後中和して製品とする。各々の樹脂で試験法
Aによりゲルタイムタイムを測定する。つぎに試験法B
にて配合糊を作り合板を作成し、合板の接着力、放出ホ
ルムアルデヒドを測定する。結果を表2に示す。
Examples 4, 5 and 6 Corresponding to Examples 1 to 3, similarly, urea and 37% formalin were charged and dissolved by heating in a predetermined amount under alkaline conditions, and the primary reaction was carried out at 90 ° C. for 30 minutes and then under acidic condition. Then, a predetermined amount of urea is charged at 80 ° C. and reacted for 4 hours. Upon cooling, at 60 ° C., a predetermined amount of glyoxal corresponding to Examples 1 to 3 was added, and the mixture was left for 30 minutes and neutralized to obtain a product. Gel time is measured according to Test Method A for each resin. Next, test method B
Make a compounded paste to make a plywood, and measure the adhesive strength of the plywood and the formaldehyde emission. The results are shown in Table 2.

【0016】比較例1〜3 実施例1〜3に対応して同じく尿素、37%ホルマリン
を仕込みアルカリ性にて所定量加熱溶解し、一次反応
90℃で30分実施後、酸性下にて80℃で尿素の所定
量を遂時仕込み、4時間反応させる。中和後冷却製品と
する。試験法Aの方法で実施例1〜3によりゲルタイム
タイム、残留ホルムアルデヒドを測定する。つぎに試験
法Bにて配合糊を作り合板を作成し、合板の接着力、放
出ホルムアルデヒド量を測定する。結果を表2に示す。
Comparative Examples 1 to 3 In the same manner as in Examples 1 to 3, urea and 37% formalin were charged, and a predetermined amount was heated and dissolved in an alkaline solution to carry out the primary reaction.
After carrying out at 90 ° C. for 30 minutes, a predetermined amount of urea is charged at 80 ° C. under acidic condition and reacted for 4 hours. Cooled product after neutralization. Gel time and residual formaldehyde are measured according to Examples 1 to 3 by the method of Test Method A. Next, a compounding paste is prepared by Test Method B to prepare plywood, and the adhesive strength of the plywood and the amount of formaldehyde released are measured. The results are shown in Table 2.

【0017】実施例9 メラミンおよび46%ホルマリンを表3に示した量を仕
込み、アルカリ性下にて90℃で4時間反応させ、真空
にて固形分62wt%にして冷却後グリオキザールを表
通り添加し製品とする。試験法Cにてゲルタイムを測定
する。つぎに試験法Dにてパーチクルボードを作成し物
性および放出ホルムアルデヒド量を測定した。結果を表
3に示す。
Example 9 Melamine and 46% formalin in the amounts shown in Table 3 were charged, reacted under alkaline conditions at 90 ° C. for 4 hours, cooled to a solid content of 62 wt% under vacuum, and glyoxal was added as shown after cooling. And Gel time is measured by Test Method C. Next, a particle board was prepared by Test Method D, and the physical properties and the amount of formaldehyde released were measured. The results are shown in Table 3.

【0018】比較例6 メラミンおよび46%ホルマリンを表3に示した量を仕
込みアルカリ性下にて90℃で4時間反応させ真空にて
固形分60wt%にして冷却製品とする。試験法C、D
にてゲルタイムを測定し次にパーチクルボードを作成し
同じ試験法にて物性、放出ホルムアルデヒド量、及び物
性試験を行った。結果を表3に示す。
Comparative Example 6 Melamine and 46% formalin were added in the amounts shown in Table 3 and reacted under alkaline conditions at 90 ° C. for 4 hours to give a solid content of 60 wt% under vacuum to obtain a cooled product. Test method C, D
Then, the gel time was measured, then a particle board was prepared, and the physical properties, the amount of formaldehyde released, and the physical properties were tested by the same test method. The results are shown in Table 3.

【0019】実施例10 比較例3の尿素樹脂70部と比較例4のメラミン樹脂3
0部を配合してグリオキザールを表3に示す量添加す
る。試験法C、試験法Dにて、ゲルタイム、物性、放出
ホルムアルデヒドを測定した。結果を表3に示す。
Example 10 70 parts of urea resin of Comparative Example 3 and melamine resin 3 of Comparative Example 4
0 parts are compounded and glyoxal is added in the amount shown in Table 3. Gel time, physical properties, and released formaldehyde were measured by Test Method C and Test Method D. The results are shown in Table 3.

【0020】比較例7 比較例3の尿素樹脂70部と比較例4のメラミン樹脂3
0部を配合して、試験法C、試験法Dにて、ゲルタイ
ム、物性、放出ホルムアルデヒドを測定する。結果を表
3に示す。
Comparative Example 7 70 parts of the urea resin of Comparative Example 3 and the melamine resin 3 of Comparative Example 4
0 parts are blended, and gel time, physical properties, and released formaldehyde are measured by Test Method C and Test Method D. The results are shown in Table 3.

【0021】実施例11 比較例4のメラミン樹脂80部とフェノール樹脂(三井
東圧化学製 ユーロイド883P)を15部配合して表
3に示す量のグリオキザールを添加する。試験法C、試
験法Dにて樹脂のゲルタイム、パーチクルボードの物
性、放出ホルムアルデヒドを測定した。結果を表3に示
す。
Example 11 80 parts of the melamine resin of Comparative Example 4 and 15 parts of a phenol resin (Euroid 883P manufactured by Mitsui Toatsu Chemicals Inc.) were mixed and the amount of glyoxal shown in Table 3 was added. In Test Method C and Test Method D, the gel time of the resin, the physical properties of the particle board, and the released formaldehyde were measured. The results are shown in Table 3.

【0022】比較例8 比較例4のメラミン樹脂80部とフェノール樹脂(三井
東圧化学製 ユーロイド883P)を20部配合して試
験法C、試験法Dにて樹脂のゲルタイム、パーチクルボ
ードの物性、放出ホルムアルデヒドを測定する。結果を
表3に示す。
Comparative Example 8 80 parts of the melamine resin of Comparative Example 4 and 20 parts of a phenol resin (Euroid 883P manufactured by Mitsui Toatsu Kagaku Co., Ltd.) were mixed and the gel time of the resin, the physical properties of the particle board and the release were measured by Test Method C and Test Method D. Measure formaldehyde. The results are shown in Table 3.

【0023】[0023]

【表2】 [Table 2]

【0024】[0024]

【表3】 [Table 3]

【0025】[0025]

【発明の効果】本発明の接着剤組成物によると、残留ホ
ルムアルデヒドを低く抑えながらゲルタイムを短く維持
して生産性を向上でき、且つ、接着強度、曲げ強度等の
物性も向上させ、耐水物性も維持できるので産業に利す
るところ極めて大である。
EFFECTS OF THE INVENTION According to the adhesive composition of the present invention, it is possible to improve the productivity by keeping the gel time short while keeping the residual formaldehyde low, and also improve the physical properties such as adhesive strength and bending strength, and also the water resistance. Since it can be maintained, it is extremely beneficial to the industry.

フロントページの続き (72)発明者 貝ケ石 博之 大阪府高石市高砂1丁目6番地 三井東圧 化学株式会社内Front page continuation (72) Inventor Hiroyuki Kaigaishi 1-6 Takasago, Takaishi-shi, Osaka Mitsui Toatsu Chemical Co., Ltd.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】ホルムアルデヒドを主剤とする水溶性アミ
ノプラスト樹脂100重量部に対して、グリオキザール
を0.2〜20重量部添加したことを特徴とする木質材
用接着剤。
1. An adhesive for wood materials, characterized in that 0.2 to 20 parts by weight of glyoxal is added to 100 parts by weight of a water-soluble aminoplast resin containing formaldehyde as a main component.
【請求項2】ホルムアルデヒを主剤とするアミノプラス
ト樹脂の他方の主剤であるアミノ化合物が、尿素単独ま
たはメラミン単独または尿素とメラミン併用である請求
項1記載の木質材用接着剤。
2. The adhesive for wood materials according to claim 1, wherein the amino compound which is the other main component of the aminoplast resin containing formaldehyde as the main component is urea alone, melamine alone or urea and melamine in combination.
【請求項3】水性アミノプラスト樹脂の含有遊離ホルム
アルデヒドを1wt%以下とした、請求項1記載の木質
材用接着剤。
3. The adhesive for wood materials according to claim 1, wherein the content of free formaldehyde contained in the aqueous aminoplast resin is 1 wt% or less.
JP27153793A 1993-10-29 1993-10-29 Adhesive for wood materials Pending JPH07126596A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP27153793A JPH07126596A (en) 1993-10-29 1993-10-29 Adhesive for wood materials

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27153793A JPH07126596A (en) 1993-10-29 1993-10-29 Adhesive for wood materials

Publications (1)

Publication Number Publication Date
JPH07126596A true JPH07126596A (en) 1995-05-16

Family

ID=17501450

Family Applications (1)

Application Number Title Priority Date Filing Date
JP27153793A Pending JPH07126596A (en) 1993-10-29 1993-10-29 Adhesive for wood materials

Country Status (1)

Country Link
JP (1) JPH07126596A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015032458A1 (en) * 2013-09-04 2015-03-12 Fraunhofer-Gesellschaft Zur Forderung Der Angewandten Forschung E.V. Wood product or natural fiber composite material product and use of a formaldehyde-free aminoplast resin for the production thereof
WO2015032733A1 (en) * 2013-09-04 2015-03-12 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e. V. Formaldehyde-free amino or amide resins based on a reactive protective group and a di- or trialdehyde as a crosslinking agent

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015032458A1 (en) * 2013-09-04 2015-03-12 Fraunhofer-Gesellschaft Zur Forderung Der Angewandten Forschung E.V. Wood product or natural fiber composite material product and use of a formaldehyde-free aminoplast resin for the production thereof
WO2015032733A1 (en) * 2013-09-04 2015-03-12 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e. V. Formaldehyde-free amino or amide resins based on a reactive protective group and a di- or trialdehyde as a crosslinking agent
DE102013014641B4 (en) 2013-09-04 2018-07-12 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Wood product or natural fiber composite product and use of a formaldehyde-free aminoplast resin for their preparation

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