JPS58222173A - Adhesive composition - Google Patents

Adhesive composition

Info

Publication number
JPS58222173A
JPS58222173A JP10552982A JP10552982A JPS58222173A JP S58222173 A JPS58222173 A JP S58222173A JP 10552982 A JP10552982 A JP 10552982A JP 10552982 A JP10552982 A JP 10552982A JP S58222173 A JPS58222173 A JP S58222173A
Authority
JP
Japan
Prior art keywords
urea
hcho
plywood
resin
formaldehyde
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
JP10552982A
Other languages
Japanese (ja)
Inventor
Heijiro Yanagi
柳 平次郎
Toshiaki Mutsutani
六谷 敏明
Masaru Odagiri
小田桐 勝
Kazuaki Yamada
和明 山田
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 JP10552982A priority Critical patent/JPS58222173A/en
Publication of JPS58222173A publication Critical patent/JPS58222173A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE:To provide an adhesive composition which emits only a small amount of free HCHO and has high temporary adhesive strength and bonding power and excellent water resistance, prepared by adding HCHO, urea and a specified inorganic metal salt to an amino resin. CONSTITUTION:1-10pts.wt. HCHO, uea in such an amount that the molar ratio of HCHO to urea may be 1.0-1.5, and 1-20pts.wt. inorganic metal salt excluding alkali metal halide (e.g. Na2SO4) are added to 100pts.wt. (on a solid basis) amino resin (e.g. melamine resin). EFFECT:The adhesive composition shows a high initial bonding strength and minimizes cold pressing time in the manufacture of plywood which may employ veneers with a high water content of 20-25%, thus producing plywood, particle board, etc. which emit only a small amount of HCHO without lowering the water resistance of the products.

Description

【発明の詳細な説明】 本発明は放出ホルムアルデヒド針の少い合板、パーティ
クルボード及びファイバーボード等の製造に使用される
接着剤組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to adhesive compositions for use in the manufacture of plywood, particleboard, fiberboard, etc., which have low formaldehyde emission needles.

近年合板、パーティクルボード及びファイバーボードか
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により夫々合板お
よびパーティ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, particleboard, and fiberboard on the human body, and the amount of formaldehyde emitted from plywood and particleboard is regulated by the Japanese Agricultural Standards and the Japanese Industrial Standards, respectively.

合板およびパーティ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なくとも1
種とホルムアルデヒドを主原料とムアルデヒド量を規制
する為には、尿素系化合物、フェノール系化合物、メラ
ミンに対するホルムアルデヒドのモル比を低くする必要
があるが、これでは合板製造時における冷圧後の初期接
着力が小さくなり、得られる合板およびパーティクルボ
ードの接着力および耐水性が低下する問題がある。
For the production of plywood and particleboard, at least one of urea compounds, phenolic compounds and melamine is used.
Seeds and formaldehyde are the main raw materials, and in order to control the amount of formaldehyde, it is necessary to lower the molar ratio of formaldehyde to urea compounds, phenolic compounds, and melamine. There is a problem that the force is reduced and the adhesive strength and water resistance of the resulting plywood and particle board are reduced.

合板製造時における冷圧後の初期接着力(以下仮接着と
略す)を向上させるにはポリビニルアルコールおよびポ
リアクリルアミドの様なビニル系高分子化合物を添加す
る方法が公知であるが、得られる接着剤が増粘したり、
耐水性をさらに低下させる等の欠点がある。
In order to improve the initial adhesion strength after cold pressing during plywood production (hereinafter referred to as temporary adhesion), it is known to add vinyl polymer compounds such as polyvinyl alcohol and polyacrylamide, but the resulting adhesive becomes thicker,
There are drawbacks such as further deterioration of water resistance.

また耐水性を維持する為には、アミン樹脂中のメラミン
量、フェノール量などを増加させる方法が考えられるが
、これでは接着剤両路を大巾に高くする欠点がある。
In order to maintain water resistance, it is possible to increase the amount of melamine, phenol, etc. in the amine resin, but this has the disadvantage of making the width of both adhesive paths significantly higher.

本発明は、接着剤価格を大巾に高める車なく1]つ仮接
着、接着力および耐水性に問題を与える事なく、放出ホ
ルムアルデヒドの少ない合板およびパーティクルボード
の製造に適した接着剤組成物を提供する事を目的とする
ものである。
The present invention provides an adhesive composition suitable for the production of plywood and particleboard that releases less formaldehyde and does not pose problems in temporary adhesion, adhesion strength and water resistance, without significantly increasing the cost of adhesives. The purpose is to provide.

本発明者は、これ等の課題を達成する為に観音研究の結
果本発明に到達した。
The present inventor has arrived at the present invention as a result of research on Kannon in order to accomplish these problems.

すなわち本発明は、アミン樹脂に、(a)ホルムアルデ
ヒド、(b)尿素、及び(C)アルカリ金属・・ロゲン
化物を除く無機金属塩類を添加する串を特徴とする接着
剤組成物である。
That is, the present invention is an adhesive composition characterized by a skewer in which (a) formaldehyde, (b) urea, and (C) inorganic metal salts other than alkali metal chlorides are added to an amine resin.

本発明におけるアミノ樹脂とは尿素樹脂、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及
びそれらとフェノール樹脂、レゾルシノールItJ]L
  )ルエン樹脂、ギシレン樹脂等との混合物または共
縮合樹脂が含まれる1、また上記樹脂にポリビニルアル
コールやセルロース系増粘剤を添加してもよい。
Amino resins in the present invention include urea resins, melamine resins, benzoguanamine resins, acetoguanamine resins, thiourea resins, or mixtures thereof, or cocondensation resins with them, phenolic resins, resorcinol ItJ]L
1) Contains a mixture or co-condensation resin with a luene resin, a cylene resin, etc. Polyvinyl alcohol or a cellulose thickener may be added to the above resin.

本発明において用いられるホルムアルデヒドは液状のホ
ルマリンでも固体のパラホルムアルデヒドでも良く、添
加量はアミノ樹脂固型分100重量部に対してホルムア
ルデヒド純分として1〜10重量部である事が好ましい
。添加量が1重量部未満の場合は効果が期待出来ず、1
0重量部を越える場合には放出ホルムアルデヒド量への
影響が大きく実用的ではない。
The formaldehyde used in the present invention may be liquid formalin or solid paraformaldehyde, and the amount added is preferably 1 to 10 parts by weight as a pure formaldehyde content per 100 parts by weight of the amino resin solid content. If the amount added is less than 1 part by weight, no effect can be expected;
If it exceeds 0 parts by weight, the amount of formaldehyde released will be greatly affected and is not practical.

本発明におけるアルカリ金属ノ・ロゲン化物を除く無機
金属塩類としては、カルシウム、銅、マグネシウム、佃
鉛、アルミニウム等のアルカリ金属以外の金属の硫酸塩
、硝酸塩、燐酸塩、炭酸塩、酸化物、ハロゲン化物、ナ
トリウムおよびカリウムなどのアルカリ金属の硫酸塩、
硝酸塩、燐酸塩、炭酸塩、酸化物があるが、望ましくは
硫酸す) IJウノ1、硫酸アルミニウム、塩化カルシ
ウム等があげられる。
Inorganic metal salts other than alkali metal halides in the present invention include sulfates, nitrates, phosphates, carbonates, oxides, and halogens of metals other than alkali metals such as calcium, copper, magnesium, lead, and aluminum. oxides, sulfates of alkali metals such as sodium and potassium,
Examples include nitrates, phosphates, carbonates, and oxides, preferably sulfuric acid, IJ Uno 1, aluminum sulfate, and calcium chloride.

これらの無機金属塩類の添加量は、アミン樹脂固形分1
00亜酸部に対し、1〜20貫量部である事が好ましい
。添加量が1重量部未満の場合にはその効果が期待出来
ず、20重量部を越える場合には接着力および奸]水性
が低下する。
The amount of these inorganic metal salts added is based on the solid content of amine resin 1
It is preferably 1 to 20 parts by weight per 00 parts by weight. If the amount added is less than 1 part by weight, no effect can be expected, and if it exceeds 20 parts by weight, the adhesive strength and water resistance will decrease.

無機金属塩類として塩化ナトリウムの様なアルカリ金属
ハロゲン化物を用いる場合には、仮接着および耐水性等
において本発明で言う様な効果は期待出来ない。
When an alkali metal halide such as sodium chloride is used as the inorganic metal salt, the effects mentioned in the present invention cannot be expected in terms of temporary adhesion, water resistance, etc.

本発明において尿素は、添加するホルムアルデヒドとの
モル比がホルムアルデヒド/尿素=10〜15である事
が好ましい。モル比が10未満の場合には接肘力Hよひ
而・l水性の低下が懸念され、15を越える場合には合
板およびパーティクルボードからの放出ホルムアルデヒ
ドが増す。
In the present invention, it is preferable that the molar ratio of urea to formaldehyde to be added is formaldehyde/urea = 10 to 15. If the molar ratio is less than 10, there is a concern that the elbow contact force will decrease in aqueous properties, and if it exceeds 15, formaldehyde released from plywood and particle board will increase.

本発明において、上記したポルノ・アルデヒド、尿素お
よびアルカリ金属ハロゲン化物を除<無情金属塩類をア
ミノ樹脂に添加する方法は、王者を別々に添加しても、
三者の中の王者を予め混合し2て冷加し残りの一考を別
に添加しても、三者を予め混合してから添加してもその
効果は変らない。
In the present invention, the above-mentioned pornographic aldehyde, urea and alkali metal halide can be removed.
Even if the king of the three is mixed in advance, cooled, and the remaining ingredients are added separately, or if the three are mixed in advance and then added, the effect remains the same.

またこの中で尿素とホルムアルデヒドを予め共存させる
場合、それぞれが七ツマ−のまま存在していて尿素ホル
ムアルデヒド非樹脂状縮合物とじて存在1−でいてもそ
の効果は変らない。
Furthermore, when urea and formaldehyde are allowed to coexist in advance, the effect does not change even if each exists as a 7-mer and 1- as a urea-formaldehyde non-resinous condensate.

本発明の構成要件のうち、(a)ホルムアルデヒド、(
1))尿素および(C)アルカリ金属ハロゲン化物を除
く無機金属塩類のどの成分が欠けても本発明でいう効果
は期待出来ず、例えば(a)ホルムアルデヒドが欠ける
と接着力、耐水性の点で不充分であり、(1))尿素が
欠けると放出ホルムアルデヒドが増加してしまう。また
(c)アルカリ金属ハロゲン化物を除く無機金属塩類が
欠けると接着力および耐水性が不安定どなる。これに対
l一本発明の構成要件の3者がアミン樹脂と共存する事
より初めて接着剤価格を大巾に高める事なく、仮接着、
接着力および耐水性に問題を与える事なく放出ホルムア
ルデヒドの少ない合板およびパーティクルボードを製造
する事が可能となる。
Among the constituent elements of the present invention, (a) formaldehyde, (
1)) If any component of the inorganic metal salts other than urea and (C) alkali metal halides is missing, the effect referred to in the present invention cannot be expected. For example, if (a) formaldehyde is missing, adhesive strength and water resistance will be affected. (1) Lack of urea results in increased formaldehyde release. Furthermore, if (c) inorganic metal salts other than alkali metal halides are missing, the adhesive strength and water resistance become unstable. In contrast, the coexistence of the three constituent elements of the present invention with the amine resin makes it possible to achieve temporary adhesion without significantly increasing the adhesive price.
It becomes possible to produce plywood and particle board that emit less formaldehyde without causing problems in adhesive strength and water resistance.

本発明の実施においては、従来より用いられている増量
剤とし切手麦粉の他に大麦粉、米粉、木粉、タルク、ク
レー等を用いたり仮接着向上を目的とするポリビニルア
ルコール等の化合物、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、撥水性向上
の為に用いられているワックスエマルジョン等を併用す
る事は何ら差支えない。
In the practice of the present invention, barley flour, rice flour, wood flour, talc, clay, etc. may be used as extenders in addition to the conventionally used stamp flour, and compounds such as polyvinyl alcohol for the purpose of improving temporary adhesion may be used. There is no problem in using together blood meal, soybean flour, corn flour, which are used as a countermeasure for high moisture content veneers, and wax emulsion, which is used to improve water repellency.

本発明の方法によれば、合板およびパーティクルボード
からの放出ホルムアルデヒドを低くする為にアミノ樹脂
としてホルムアルデヒドと尿素、メラミン等のアミン化
合物とのモル化の低いものを用いても、合板製造時の初
期接着力が高く、冷用圧締時間が短かくて済み、又20
〜25%といった高含水率単板を使用する事が可能であ
り、合板パーティクルボードの耐水性を低下させる事な
く、放出ホルムアルデヒドの低い製品を製造する事が可
能である。
According to the method of the present invention, in order to reduce formaldehyde released from plywood and particleboard, even if an amino resin with a low molar ratio of formaldehyde and amine compounds such as urea and melamine is used, it is possible to High adhesive strength, short cold pressing time, and 20
It is possible to use veneers with high moisture content, such as ~25%, and it is possible to produce products with low formaldehyde emissions without reducing the water resistance of plywood particleboard.

さらに本発明の方法によれば、上記目的以外にも高含水
率単板チップを使用した時の合板パーティクルボード、
ファイバーボードのパンク防止がはかれる。
Further, according to the method of the present invention, in addition to the above-mentioned purposes, plywood particle board when using high moisture content veneer chips,
The fiberboard is protected from punctures.

この様に本発明は、ホルムアルデヒド放散の低い合板お
よびパーティクルボードの製造において実用上の価値は
高い。
As described above, the present invention has high practical value in the production of plywood and particle board with low formaldehyde emission.

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係は木破率および吸水厚さ膨
張率に関する係以外はすべて重量部を示す。又、部は重
量部を示す。
Next, the present invention will be specifically explained using Examples and Comparative Examples. All terms in the text below refer to parts by weight, except for those relating to wood breakage rate and water absorption thickness expansion rate. Moreover, parts indicate parts by weight.

実施例1 尿素樹脂(三井東圧化学株製、商品名U−701、樹脂
分52%)100部に対して硫酸ナトリウム4部、37
%ホルマリン7部、尿素2部を加え、さらに小麦粉20
部、水16部、塩化アンモニウム1部を加え攪拌して合
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。合板の性能を表−1に示した。
Example 1 4 parts of sodium sulfate, 37 parts per 100 parts of urea resin (manufactured by Mitsui Toatsu Chemical Co., Ltd., trade name U-701, resin content 52%)
Add 7 parts formalin, 2 parts urea, and add 20 parts flour.
1 part, 16 parts of water, and 1 part of ammonium chloride were added and stirred to obtain an adhesive compounded paste for plywood, and plywood was manufactured using the compounded paste under the following bonding conditions. The performance of plywood is shown in Table 1.

単板1−i’7成: 0.6 + 1.3 + 0.6
−+、/−ノ各厚ミカらなるラワン3プライ構成 単板含水率:原板中板共7〜10係 塗付量: 25g7900m 堆積時間=20旗η 冷圧条件: 、、1′;、2幻/7、ISO?+1虎熱
圧条件: 10 kq/cl、 120°0,50Jシ
O実施例2 尿素樹脂U−701(前出)100部に苅して、予め硫
酸ナトリウム4部、67係ホルマリン7部、尿素2部、
水10部を加熱混合してお℃・たものを加え、さらに小
麦粉20部、水6部、塩化アンモニウム1部を加え、攪
拌混合して合板用接着剤配合糊を得た。
Veneer 1-i'7 composition: 0.6 + 1.3 + 0.6
-+, /- thickness lauan 3-ply veneer composition Moisture content: 7 to 10 for both original plate and middle plate Coating amount: 25 g 7900 m Deposition time = 20 flags η Cold pressure conditions: ,, 1';, 2 Illusion/7, ISO? +1 heat and pressure conditions: 10 kq/cl, 120° 0.50 J SiO Example 2 100 parts of urea resin U-701 (mentioned above) was coated with 4 parts of sodium sulfate, 7 parts of formalin 67, and urea. 2nd part,
10 parts of water was heated and mixed and heated to a temperature of 0.degree. C., and further 20 parts of wheat flour, 6 parts of water, and 1 part of ammonium chloride were added and mixed with stirring to obtain an adhesive compound paste for plywood.

実施例1と同一の接着条件で合板を製造した。Plywood was manufactured under the same bonding conditions as in Example 1.

その性能を表−1に示l〜だ1、 実施例3 尿素樹脂の代りに、尿素メラミン共縮合樹脂(三井東圧
化学■製、商品名、u−350)を、イ1iii酸ナト
リウムの代りに硫酸アルミニウムを用いて実施例1と同
一の条件で合板を製造し、その性能を表−1に示した。
Its performance is shown in Table 1. Example 3 Instead of urea resin, urea melamine cocondensation resin (manufactured by Mitsui Toatsu Chemical Co., Ltd., trade name, U-350) was used instead of sodium iliiiate. Plywood was manufactured using aluminum sulfate under the same conditions as in Example 1, and its performance is shown in Table 1.

実施例4〜9 アミン樹脂、ホルムアルデヒド、無機金属塩および尿素
を表−1に示す割合で撹拌混合し、合板用接着剤組成物
を得た。
Examples 4 to 9 Amine resin, formaldehyde, inorganic metal salt, and urea were stirred and mixed in the ratios shown in Table 1 to obtain adhesive compositions for plywood.

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, and its performance is shown in Table 1.

比較例1〜8 アミン樹脂に対してホルムアルデヒド、無機金属塩、尿
素を表−1に示す割合で攪拌混合し或いは添加せずに、
合板用接着剤配合糊を得た。
Comparative Examples 1 to 8 Formaldehyde, inorganic metal salt, and urea were stirred and mixed with the amine resin in the proportions shown in Table 1, or without addition.
An adhesive compounded paste for plywood was obtained.

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, and its performance is shown in Table 1.

実施例10 尿素樹脂(ヨ井東圧化学株製、商品名U755、樹脂分
65チ)、硫酸ナトリウム37係ホルマリン、尿素、水
、塩化アンモニウムを用いて以下の様なパーティクルボ
ード用配合糊を得た。
Example 10 Using urea resin (manufactured by Yoi Toatsu Kagaku Co., Ltd., trade name U755, resin content 65%), sodium sulfate formalin, urea, water, and ammonium chloride, the following compounded glue for particle board was obtained. .

硫酸ナトリウム        55 37%ホルマリン       88 尿  素             55水     
          52      25塩化アンモ
ニウム        05       1」二記配
合糊を使用して下記接着条件にてパーティクルボードを
製造した。パーティクルボードの+′1能を表−2に示
した。
Sodium sulfate 55 37% formalin 88 Urea 55 Water
52 25 Ammonium Chloride 05 1" Particle board was manufactured using the compounded glue described in "2" under the following bonding conditions. Table 2 shows the +'1 ability of particle board.

機種構成  : ラワンチップを用いた6層(II′]
′成比   重   二07 板  J享  :13mm チップ含水率 二 表層、丈層共に3%樹脂吹付率  
: (表層)12係、(た層)7係マツト含水率 = 
(表層)20%、(毛屑)10チ熱圧条件  : 15
0°0.4 mLr+Lr側11 実施例10の樹脂吹伺率を2係ずつ真らしく表層)10
受、(止層)5係とし、他の接看条件は変わらないよう
にしてパーティクルボードを製造した。その時の配合及
びパーティクルボードの性能を表−2に示した。
Model configuration: 6 layers using lauan chip (II')
207 Plate J: 13mm Chip moisture content 2 3% resin spraying rate for both surface layer and length layer
: (Surface layer) 12th layer, (top layer) 7th layer pine moisture content =
(Surface layer) 20%, (hair waste) 10 pieces Heat and pressure conditions: 15
0°0.4 mLr+Lr side 11 Increase the resin blowing rate of Example 10 by 2 factors (surface layer) 10
Particleboard was produced with five receiving and (stopping) layers and other viewing conditions unchanged. The formulation and performance of the particle board at that time are shown in Table 2.

実施例12 尿素41,1脂の代りに尿素メラミン樹脂(三井東圧化
学株製、商品名U 775、樹脂分65俸)を、又、硫
酸ナトリウムの代りに硫酸アルミニウムを用いて実施例
10と同一の条件でパーティフルボ1 一ドを製造した。パーティクルボード9性能を衣−2に
示した。
Example 12 Example 10 was performed using urea melamine resin (manufactured by Mitsui Toatsu Chemical Co., Ltd., trade name U 775, resin content 65 yen) in place of urea 41,1 fat, and aluminum sulfate in place of sodium sulfate. Partifrucon 1 was produced under the same conditions. Particle board 9 performance is shown in Cloth-2.

実7(i+j例13 尿素樹脂の代りに尿素メラミン樹脂U755(前出)を
又、硫酸ナトリウムの代りに硫酸アルミニウムを用いて
実施例11と同一の条件でパーティクルボードを製造し
た。パーティクルボードの性能を表−2に示した。
Example 7 (i+j Example 13 Particle board was manufactured under the same conditions as Example 11 using urea melamine resin U755 (described above) instead of urea resin and aluminum sulfate instead of sodium sulfate. Performance of particle board are shown in Table-2.

比較例9〜12 アミン樹脂に対してホルムアルデヒド、無機金属塩、尿
素を表−2に示す割合で攪拌混合し、或いは添加せずに
パーティクルボード用配合糊を得た。これを用いて実施
例10と同一条件でパーティクルボードを製造した。パ
ーティクルボードの性能を表−2に示した。
Comparative Examples 9 to 12 Formaldehyde, inorganic metal salt, and urea were stirred and mixed with amine resin in the ratios shown in Table 2, or a compounded paste for particle board was obtained without adding them. Using this, a particle board was manufactured under the same conditions as in Example 10. The performance of particle board is shown in Table 2.

2 (注釈) 表−1 (1)合板製造工程中の冷圧終了後の構成単板の接着状
態の事である。
2 (Notes) Table 1 (1) This refers to the adhesion state of the constituent veneers after cold pressing during the plywood manufacturing process.

(2)普通合板の日本農林規格(以下、JASと略す)
に従った。に)内の数値は木破率を示す。これは耐水接
着力についても同様。
(2) Japanese Agricultural Standards for Ordinary Plywood (hereinafter abbreviated as JAS)
I followed. Figures in ) indicate the wood breakage rate. The same applies to water-resistant adhesive strength.

(3)実施例345はJASの魚沸操返し試1験を行い
、それ以外は温冷水浸漬試、験を行った。
(3) Example 345 was subjected to one JAS fish boiling test, and the other samples were subjected to hot and cold water immersion tests.

(4)JASに定められたデシケータ−法で行った。(4) The desiccator method specified by JAS was used.

表−2 (1)性能試験は日本農林規格JIS −A 5908
の方法に従う。
Table 2 (1) Performance test is based on Japanese Agricultural Standards JIS-A 5908
Follow the method.

但し70°02Jrの吸水厚さ膨張率は、湿潤曲げ試恢
片を用いて両足した。
However, the water absorption thickness expansion coefficient of 70°02Jr was measured using a wet bending specimen.

特許出願人 三井東圧化学株式会社 6Patent applicant Mitsui Toatsu Chemical Co., Ltd. 6

Claims (1)

【特許請求の範囲】[Claims] (1)アミン樹脂に、(a)ホルムアルデヒド、(b)
尿素及び(C)アルカリ金属ハロゲン化物を除く無機金
属塩類、を添加する事を特徴とする接着剤組成物。 項記載の接着剤組成物。
(1) Amine resin, (a) formaldehyde, (b)
An adhesive composition characterized by adding urea and (C) inorganic metal salts other than alkali metal halides. The adhesive composition described in .
JP10552982A 1982-06-21 1982-06-21 Adhesive composition Pending JPS58222173A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10552982A JPS58222173A (en) 1982-06-21 1982-06-21 Adhesive composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10552982A JPS58222173A (en) 1982-06-21 1982-06-21 Adhesive composition

Publications (1)

Publication Number Publication Date
JPS58222173A true JPS58222173A (en) 1983-12-23

Family

ID=14410112

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10552982A Pending JPS58222173A (en) 1982-06-21 1982-06-21 Adhesive composition

Country Status (1)

Country Link
JP (1) JPS58222173A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0249747A2 (en) * 1986-05-17 1987-12-23 BASF Aktiengesellschaft Hardening composition for the hardening of an urea-formaldehyde adhesive, and its use in the glueing of chipboard
US7235613B2 (en) * 2001-10-18 2007-06-26 Akzo Nobel N.V. Method of gluing wood based materials

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0249747A2 (en) * 1986-05-17 1987-12-23 BASF Aktiengesellschaft Hardening composition for the hardening of an urea-formaldehyde adhesive, and its use in the glueing of chipboard
US7235613B2 (en) * 2001-10-18 2007-06-26 Akzo Nobel N.V. Method of gluing wood based materials
US7452442B2 (en) 2001-10-18 2008-11-18 Akzo Nobel N.V. Gluing wood based materials with melaminic amino resin and resorcinol or tannin resin

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