JPH11156820A - Production of particle board - Google Patents

Production of particle board

Info

Publication number
JPH11156820A
JPH11156820A JP32297997A JP32297997A JPH11156820A JP H11156820 A JPH11156820 A JP H11156820A JP 32297997 A JP32297997 A JP 32297997A JP 32297997 A JP32297997 A JP 32297997A JP H11156820 A JPH11156820 A JP H11156820A
Authority
JP
Japan
Prior art keywords
melamine
urea resin
resin
urea
reaction
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
JP32297997A
Other languages
Japanese (ja)
Inventor
Takeshi Kikuchi
丈志 菊地
Atsushi Ito
敦 伊藤
Koji Matsunaga
幸治 松永
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 Chemicals Inc
Original Assignee
Mitsui 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 Chemicals Inc filed Critical Mitsui Chemicals Inc
Priority to JP32297997A priority Critical patent/JPH11156820A/en
Publication of JPH11156820A publication Critical patent/JPH11156820A/en
Pending legal-status Critical Current

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  • Dry Formation Of Fiberboard And The Like (AREA)

Abstract

PROBLEM TO BE SOLVED: To increase curing speed of a particle board excellent in water resistance and strength with the use of a melamine resin adhesive, and to improve productivity. SOLUTION: A urea resin and a liquid melamine urea resin adhesive obtained by reacting a mixture of formaldehyde/melamine/urea/methanol in a mole ratio of 2.2-6.0/1/0.1-1.0/0.05-1.0 are mixed in a ratio of 8/2-3/7, the mixture is added with wood chips to be hot-pressed. In this way, a particle board which indicates only a small variation of curing time in a blend ratio and does not require the change of press conditions and the amount of a curing agent.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、メラミン樹脂と尿
素樹脂による接着剤を木質チップに添加し加熱圧締する
ことによりパーティクルボードを製造する方法に関する
ものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a particle board by adding an adhesive made of a melamine resin and a urea resin to a wood chip and heating and compressing the chip.

【0002】[0002]

【従来の技術】木材の薄板,小片,繊維等を接着してな
るパーティクルボード、合板、木質繊維板等の木質系ボ
ードは,木質系資源の有効利用に役立っていることは周
知の事実である。特に、パーティクルボードは、年間約
1000万立方メートルも生じる木質系建築廃材を焼却
処分せずにリサイクルして有効利用しているので極めて
有用である。これら木質系ボードは、多くの場合アミノ
系接着剤、すなわち、メラミン樹脂やメラミン尿素樹
脂、尿素樹脂等を接着剤として使用している。メラミン
尿素系接着剤の製法には、メラミンと尿素を反応釜に同
時にまたは逐次添加でホルムアルデヒドと反応させて製
造する方法と、別々に調整したメラミン樹脂と尿素樹脂
を混合する方法がある。後者の方法により製造したメラ
ミン尿素系接着剤によれば、例えば、JIS A 59
08−1994 Mタイプの規格をクリアするパーティ
クルボードを製造する場合において、原料となる木質系
廃材からなるチップの混入割合及び廃材の比重分布、さ
らにはユーザー独自の要求品質、耐水性強度等に対応す
べく、メラミン樹脂と尿素樹脂の混合比を任意に変更す
ることが可能となる。
2. Description of the Related Art It is a well-known fact that woody boards such as particleboard, plywood, and wood fiberboard obtained by bonding thin boards, small pieces, fibers and the like of wood are useful for effective use of woody resources. . In particular, particle board is extremely useful because it recycles wood-based building waste, which is generated by about 10 million cubic meters per year, without incineration and effectively uses it. These wooden boards often use an amino adhesive, that is, a melamine resin, a melamine urea resin, a urea resin, or the like as the adhesive. As a method for producing a melamine urea-based adhesive, there are a method of producing melamine and urea by reacting them with formaldehyde simultaneously or sequentially in a reaction vessel, and a method of mixing melamine resin and urea resin separately prepared. According to the melamine urea adhesive manufactured by the latter method, for example, JIS A 59
08-1994 When manufacturing particle board that meets the M-type standard, it supports the mixing ratio of chips made of wood-based waste material and the specific gravity distribution of the waste material, as well as the user's unique required quality and water-resistant strength. Thus, the mixing ratio between the melamine resin and the urea resin can be arbitrarily changed.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、ユーザ
ーからの種々の要求グレードを満足するボードを効率よ
く製造するにあたり、例えば、耐水性を強化するには、
メラミン系接着剤のブレンド比率を上げることで種々の
耐水性グレードに対応することは周知の事実であるが、
ブレンド比によってはブレンド後の硬化時間がもとの硬
化時間の2倍近くまで遅延するという原因不明の現象が
生じ、ブレンド比率によってその都度製造条件を変更し
なければならない。また、近年社会問題となっている放
出ホルマリンに関する対応として、ホルマリンの反応モ
ル比を押さえた樹脂が製造されているが、このホルマリ
ンの低モル品といわれるものほどブレンド後の硬化時間
の遅延が著しいという問題がある。
However, in order to efficiently manufacture boards satisfying various grades required by users, for example, in order to enhance water resistance,
It is a well-known fact that by increasing the blend ratio of the melamine-based adhesive, it is possible to correspond to various water-resistant grades.
Depending on the blend ratio, an unexplained phenomenon occurs in which the curing time after blending is delayed to nearly twice the original curing time, and the production conditions must be changed each time depending on the blend ratio. In addition, as a response to released formalin, which has become a social problem in recent years, resins with a reduced molar ratio of formalin have been manufactured, but the lower the molar ratio of this formalin, the longer the curing time after blending is significantly delayed. There is a problem.

【0004】硬化時間遅延の対策としては硬化剤量の増
量、プレス時間の延長等の方法が採られるが、硬化剤量
を一定量以上増量しても硬化時間を短縮するのには限度
があり、極端に増量するとパーティクルボードが加水分
解を起こしやすくなるため耐久性に問題が生じてしま
う。また、プレス時間の延長を行うと生産性が低下し、
現実的ではない。したがって、JIS A 5908
Mタイプボードの製造において、メラミン尿素樹脂と尿
素樹脂を任意にブレンド比を変更しながらの製造方法は
確立されていなく、使用に適したメラミン尿素樹脂はな
かった。
As a countermeasure against the delay of the curing time, methods such as increasing the amount of the curing agent and extending the press time are adopted. However, even if the amount of the curing agent is increased by a certain amount or more, there is a limit in shortening the curing time. If the amount is extremely increased, the particle board is liable to be hydrolyzed, causing a problem in durability. Also, extending the press time reduces productivity,
Not realistic. Therefore, JIS A 5908
In the production of the M type board, a production method of arbitrarily changing the blend ratio of the melamine urea resin and the urea resin has not been established, and there is no melamine urea resin suitable for use.

【0005】[0005]

【課題を解決するための手段】本発明者は、メラミン尿
素樹脂と尿素樹脂の混合使用における硬化時間を少なく
するため鋭意検討の結果、通常の尿素樹脂と硬化性の高
い特定のメラミン樹脂とをブレンドすることにより、硬
化時間の延長のない、強度に優れたメラミン尿素樹脂を
得ることが可能となることを見出し、これを用いてパー
ティクルボードを製造する本発明を完成した。即ち、本
発明のパーティクルボードの製造方法は、尿素樹脂と、
ホルムアルデヒド:メラミン:尿素:メタノールのモル
比が(2.2〜6.0):(1):(0.1〜1.
0):(0.05〜1.0) で反応させて得られた液状
メラミン尿素樹脂を8:2〜3:7の割合で混合して木
質チップに添加し、加熱圧締することを特徴とするもの
である。
Means for Solving the Problems The present inventors have conducted intensive studies to reduce the curing time in the mixed use of a melamine urea resin and a urea resin. It has been found that by blending, it is possible to obtain a melamine urea resin having excellent strength without prolonging the curing time, and the present invention for producing a particle board using the melamine urea resin has been completed. That is, the method for producing a particle board of the present invention comprises the steps of:
The molar ratio of formaldehyde: melamine: urea: methanol is (2.2-6.0) :( 1) :( 0.1-1.
0): The liquid melamine urea resin obtained by the reaction of (0.05 to 1.0) is mixed at a ratio of 8: 2 to 3: 7, added to the wood chips, and heated and pressed. It is assumed that.

【0006】[0006]

【発明の実施の形態】以下、本発明について具体的に説
明する。本発明における液状メラミン尿素樹脂接着剤
は、つぎのような3工程の反応で得られる。まず、1次
反応としてホルムアルデヒド、メラミン、尿素、メタノ
ールを(2.2〜6.0):(1.0):(0〜1.
0):(0.05〜1.0)のモル比で反応させる。反
応温度は65〜90℃が望ましく、モノマーが溶解後1
0〜30分間程度反応させる。1次反応の初期pHは
6.5から9が望ましく、6.5未満では反応のコント
ロールが難しい。初期pHとは尿素及びメラミンを添加
前のホルマリンのpHである。
BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described specifically. The liquid melamine urea resin adhesive according to the present invention is obtained by the following three-step reaction. First, formaldehyde, melamine, urea, and methanol were used as primary reactions at (2.2 to 6.0): (1.0): (0 to 1.
0): The reaction is performed at a molar ratio of (0.05 to 1.0). The reaction temperature is preferably from 65 to 90 ° C.
The reaction is performed for about 0 to 30 minutes. The initial pH of the primary reaction is preferably from 6.5 to 9, and if it is less than 6.5, it is difficult to control the reaction. The initial pH is the pH of formalin before adding urea and melamine.

【0007】2次反応は、反応系にさらに尿素及び又は
メラミンを一度にまたは分割してまたは連続して添加し
行われる。反応温度は65〜85℃であり、反応pHは
7.5〜9.0である。反応終点は白濁法にて判定す
る。2次反応の終点は20〜35℃/10倍である。反
応が不十分の場合は0℃における保存安定性が低下す
る。尿素及び又はメラミン添加後の反応モル比はホルム
アルデヒド、メラミン、尿素、メタノールを(2.2〜
3.5):(1.0):(0.1〜1.0):(0.0
5〜0.6)とする。
[0007] The secondary reaction is carried out by adding urea and / or melamine to the reaction system all at once, dividedly or continuously. The reaction temperature is 65-85 ° C, and the reaction pH is 7.5-9.0. The reaction end point is determined by the cloudiness method. The end point of the secondary reaction is 20 to 35 ° C / 10 times. If the reaction is insufficient, the storage stability at 0 ° C. decreases. The reaction molar ratio after the addition of urea and / or melamine is as follows: formaldehyde, melamine, urea, methanol
3.5): (1.0): (0.1 to 1.0): (0.0
5 to 0.6).

【0008】続く3次反応は、反応モル比をそのままで
反応系のpHをNaOH、KOH等の触媒で10〜1
1.5に調整して行われる。3次反応の終点は白濁法で
30〜55℃/5倍であり、望ましくは40〜50℃/
5倍である。所定の縮合度まで反応を進めた後、樹脂液
のpHを9.5〜11.0に調整し、冷却して本発明の
透明な液状メラミン尿素樹脂が得られる。この樹脂は年
間を通じ2週間以上の安定性を有し、異常な増粘はな
い。最終のpH調整は夏季の保存安定性に大きく影響す
る。各反応工程のpH及び反応終点は正確にコントロー
ルされなければならない。また、白濁法とは、樹脂液を
水で5倍または10倍に希釈した後に徐々に冷却し樹脂
液が白濁を始める温度で樹脂の縮合度を判定する方法で
ある。
In the subsequent tertiary reaction, the pH of the reaction system is adjusted to 10 to 1 with a catalyst such as NaOH or KOH while maintaining the reaction molar ratio.
Adjusted to 1.5. The end point of the tertiary reaction is 30 to 55 ° C / 5 times by the cloudiness method, preferably 40 to 50 ° C /
5 times. After the reaction has proceeded to a predetermined degree of condensation, the pH of the resin solution is adjusted to 9.5 to 11.0 and cooled to obtain the transparent liquid melamine urea resin of the present invention. The resin has a stability of more than 2 weeks throughout the year and has no abnormal thickening. The final pH adjustment greatly affects the storage stability in summer. The pH and reaction endpoint of each reaction step must be precisely controlled. The cloudiness method is a method of diluting a resin solution 5 or 10 times with water and then gradually cooling the solution to determine the degree of condensation of the resin at a temperature at which the resin solution starts clouding.

【0009】本発明では、上記の反応で得られる液状メ
ラミン尿素樹脂を尿素樹脂と混合して木質チップの接着
剤として用いる。本発明で使用する尿素樹脂とは、とく
に限定されず、通常の水系の尿素樹脂接着剤であり、合
板やパーティクルボードの製造に供されものである。ま
た、液状メラミン尿素樹脂と尿素樹脂との混合割合は、
重量比で8:2〜3:7であり、液状メラミン尿素樹脂
の割合が、重量比で8を超えるとコストアップとなり、
また3未満では耐水性が不十分となり、好ましくない。
液状メラミン尿素樹脂と尿素樹脂との混合は、液状メラ
ミン尿素樹脂製造直後及び使用直前に攪拌装置の付いた
調整槽、タンク内で攪拌しながら混合を行うか、または
配管中に設置されたラインミキサー等で混合する。混合
後、ブレンダー内のチップに吹き付けるか、または、各
樹脂を個別ラインによりブレンダー内に同時に吹き付け
るような方法で混合した後、熱圧してパーティクルボー
ドを得ることが出来る。このように、液状メラミン尿素
樹脂接着剤とイソシアネート系接着剤を混合後または別
個に、木材チップ、木材ファイバーまたは単板等に付着
させた後に加熱圧締して木質ボードを得る。
In the present invention, the liquid melamine urea resin obtained by the above reaction is mixed with a urea resin and used as an adhesive for wood chips. The urea resin used in the present invention is not particularly limited, and is an ordinary water-based urea resin adhesive, which is provided for the production of plywood and particle board. The mixing ratio of the liquid melamine urea resin and the urea resin is
If the weight ratio is 8: 2 to 3: 7, and the ratio of the liquid melamine urea resin exceeds 8, the cost increases,
If it is less than 3, the water resistance becomes insufficient, which is not preferable.
The liquid melamine urea resin is mixed with the urea resin immediately after the liquid melamine urea resin is manufactured and immediately before use by mixing while stirring in a regulating tank or tank equipped with a stirrer, or a line mixer installed in a pipe. And mix. After mixing, the particles can be sprayed onto chips in the blender, or mixed in such a manner that each resin is simultaneously sprayed into the blender through individual lines, and then heated and pressed to obtain a particle board. As described above, after mixing the liquid melamine urea resin adhesive and the isocyanate-based adhesive or separately attaching them to a wood chip, a wood fiber, a veneer or the like, they are heated and pressed to obtain a wood board.

【0010】本発明の方法では、使用する接着剤は、ポ
ットライフ及び粘性が従来アミノ樹脂と同様であるの
で、木材チップ、木材ファイバーまたは単板等に付着さ
せる工程は既存の設備で容易に行う事ができる。さらに
接着剤の硬化性も従来のアミノ樹脂と同等以上であるの
で、既存の熱圧プレスを使用することができる。硬化条
件は、従来のメラミン樹脂等とほば同一の条件を採用で
きる。硬化剤量は、接着剤に対して、表層で0.5〜1
wt%、芯層で1〜3%程度であり、接着剤の添加量
は、木材チップ、木材ファイバーまたは単板等に対し
て、表層で9〜12wt%、芯層で3〜9wt%が望ま
しい。さらに、撥水剤としてパラフインワックス等を添
加しても何ら問題ない。
In the method of the present invention, since the adhesive used has the same pot life and viscosity as the conventional amino resin, the step of adhering it to wood chips, wood fibers or veneers can be easily carried out with existing equipment. Can do things. Further, since the curability of the adhesive is equal to or higher than that of the conventional amino resin, an existing hot press can be used. As the curing conditions, almost the same conditions as those of a conventional melamine resin or the like can be adopted. The amount of the curing agent is 0.5 to 1 in the surface layer with respect to the adhesive.
wt%, about 1 to 3% for the core layer, and the addition amount of the adhesive is preferably 9 to 12 wt% for the surface layer and 3 to 9 wt% for the core layer with respect to the wood chip, wood fiber or veneer. . Furthermore, there is no problem even if paraffin wax or the like is added as a water repellent.

【0011】[0011]

〔メラミン尿素樹脂の製造〕(Production of melamine urea resin)

製造例1(新メラミン尿素樹脂の製造) まず、1次反応は、ホルムアルデヒド、メラミン、尿
素、メタノールを(7):(1.0):(1.13):
(0.5)のモル比反応させる。反応温度は80℃
で、モノマーが溶解後20分間反応させる。1次反応の
初期pHは8.0である。2次反応は、反応系にさらに
尿素及びメラミンをホルムアルデヒド:メラミン:尿素
が(2.52):(1.0):(0.5):(0.5)
のモル比になるようにメラミン及び尿素を一括して添加
する。反応温度は70℃で、2次反応の終点は白濁法で
25℃/10倍である。続く3次反応は反応系をpHを
11.5にNaOHを用いて調製した後、反応温度は7
0℃で白濁法45℃/5倍まで反応を進め、樹脂液のp
Hを10.5に蟻酸を用いて調整した後、冷却して透明
なメラミン尿素樹脂接着剤が得られる。本樹脂は0〜3
5℃で2週間以上良好な流動性を有した。本樹脂の樹脂
特性値としては、固形分65%、比重1.29、pH1
0.5、粘度180cp、遊離ホルマリン値0.3%以
下である。
Production Example 1 (Production of New Melamine Urea Resin) First, the primary reaction was performed using formaldehyde, melamine, urea, and methanol as (7): (1.0): (1.13):
The reaction is performed at a molar ratio of (0.5). Reaction temperature is 80 ° C
And react for 20 minutes after the monomer is dissolved. The initial pH of the primary reaction is 8.0. In the secondary reaction, urea and melamine are further added to the reaction system by formaldehyde: melamine: urea (2.52) :( 1.0) :( 0.5) :( 0.5)
Melamine and urea are added all at once such that the molar ratio is as follows. The reaction temperature is 70 ° C, and the end point of the secondary reaction is 25 ° C / 10 times by the cloudiness method. In the subsequent tertiary reaction, the reaction system was adjusted to pH 11.5 using NaOH, and the reaction temperature was adjusted to 7
At 0 ° C, the reaction was advanced to 45 ° C / 5 times in the cloudiness method.
After adjusting H to 10.5 using formic acid, the mixture is cooled to obtain a transparent melamine urea resin adhesive. This resin is 0-3
It had good flowability at 5 ° C for more than 2 weeks. The resin characteristic values of this resin are as follows: solid content 65%, specific gravity 1.29, pH 1
0.5, viscosity 180 cp, free formalin value 0.3% or less.

【0012】製造例2(従来メラミン尿素樹脂の製造) ホルムアルデヒド、メラミン、尿素、メタノールを
(2.52):(1):(0.2):(1.33)のモ
ル比で反応させる。反応温度は80℃。初期pHは規定
量のNaOHを添加し、pH12で反応を進める。反応
終点は水混和性にて判定し、白濁法で7〜8倍/20℃
である。その後、樹脂液のpHを蟻酸を用いて11.0
に調整した後冷却して透明なメラミン尿素樹脂接着剤が
得られる。
Production Example 2 (Conventional Production of Melamine Urea Resin) Formaldehyde, melamine, urea and methanol are reacted in a molar ratio of (2.52) :( 1) :( 0.2) :( 1.33). Reaction temperature is 80 ° C. For the initial pH, a specified amount of NaOH is added, and the reaction proceeds at pH 12. The end point of the reaction was determined by water miscibility, and 7 to 8 times / 20 ° C by the cloudiness method.
It is. Thereafter, the pH of the resin solution was adjusted to 11.0 with formic acid.
After cooling, a transparent melamine urea resin adhesive is obtained.

【0013】〔樹脂硬化時間の測定〕各メラミン尿素樹
脂と尿素樹脂の各混合比率における硬化時間の測定を行
った。ポリカップにメラミン尿素樹脂と尿素樹脂を8:
2〜2:8の各比率にて添加し攪拌機にて混合攪拌す
る。混合後の樹脂有り姿100部に対して25%アンモ
ニア水1部、塩化アンモニウム1部を添加し、5分間混
合攪拌する。試験管に樹脂液5gを量り取り、100℃
の温水中に浸けて、JISに基づいて時間を測定した。
結果を図1に示す。
[Measurement of Curing Time of Resin] Curing time was measured at each mixing ratio of each melamine urea resin and urea resin. Melamine urea resin and urea resin in a polycup 8:
It is added at a ratio of 2-2: 8 and mixed and stirred by a stirrer. 1 part of 25% ammonia water and 1 part of ammonium chloride are added to 100 parts of the resin after mixing, and mixed and stirred for 5 minutes. Weigh 5 g of the resin solution in a test tube,
Immersed in warm water and measured the time based on JIS.
The results are shown in FIG.

【0014】〔パーティクルボードの製造〕 パーティクルボードの製造条件 ボード様式:3層ボード 使用チップ:(表層)ラワン、(芯層)ラワン チップ構成比:(表層:芯層=1:2) 樹脂吹付け前チップ含水率;表層4%、芯層2% 樹脂吹付け後チップ含水率;表層18%、芯層8% 樹脂吹付け率:表層13%、芯層7% 設定ボード厚み;16mm 設定ボード比重;0.76 熱圧温度;185℃ 熱圧時間;2分30秒、3分、3分30秒、4分、4分
30秒 硬化剤:実施例1及び2で製造した接着剤の有り姿10
0部に対して塩化アンモニウム1部、25%アンモニア
水1部を添加した。
[Manufacture of Particle Board] Manufacturing conditions of particle board Board style: 3-layer board Chip used: (surface layer) Rawan, (core layer) Rawan Chip composition ratio: (surface layer: core layer = 1: 2) Resin spraying Before chip moisture content: Surface layer 4%, core layer 2% Resin sprayed chip moisture content: Surface layer 18%, core layer 8% Resin spray rate: surface layer 13%, core layer 7% Set board thickness; 16mm Set board specific gravity 0.76 hot-press temperature; 185 ° C hot-press time: 2 minutes 30 seconds, 3 minutes, 3 minutes 30 seconds, 4 minutes, 4 minutes 30 seconds Curing agent: appearance of adhesive prepared in Examples 1 and 2 10
One part of ammonium chloride and one part of 25% aqueous ammonia were added to 0 parts.

【0015】上記条件を基本条件とし、各メラミン尿素
樹脂接着剤と尿素樹脂の各混合比率においてパーティク
ルボードを製造し、試験した結果を図2、図3、図4に
示す。残存率とは常態曲げ強さの値を100とした場合
の、湿潤曲げ強さの値を%で表したものである。ボード
試験はJIS A5908−1994に準じ評価を行な
った。
Under the above conditions as basic conditions, particle boards were manufactured at various mixing ratios of each melamine urea resin adhesive and urea resin, and the results of the tests are shown in FIGS. 2, 3 and 4. The residual ratio is the value of the wet bending strength expressed in% when the value of the normal bending strength is 100. The board test was performed according to JIS A5908-1994.

【0016】[0016]

【発明の効果】本発明の方法によれば、ブレンド比にお
ける硬化時間の変動が少なく、プレス条件、硬化剤量の
変更を要しないでパーティクルボードを製造することが
出来、使用チップの状態及び目的とする規格の製造に併
せて任意に接着剤のブレンド比の変更が可能であり、従
来の様に、ブレンド比により硬化時間が遅延し、同一硬
化剤量、同一プレス時間でも硬化不足にならないため、
生産性が向上する。また、本発明で使用するメラミン樹
脂は反応性が高く、従来のメラミン尿素樹脂と比較し
て、物性面で高い強度が得られるためメラミン樹脂の添
加比率を下げることが可能となり、強度維持のままでコ
ストダウンが可能である。
According to the method of the present invention, the variation of the curing time in the blend ratio is small, and the particle board can be manufactured without changing the pressing conditions and the amount of the curing agent. It is possible to arbitrarily change the blend ratio of the adhesive in accordance with the manufacture of the standard, and as in the past, the curing time is delayed by the blend ratio, and the curing does not become insufficient even with the same amount of the curing agent and the same pressing time ,
Productivity is improved. In addition, the melamine resin used in the present invention has high reactivity and, compared with the conventional melamine urea resin, can obtain a high strength in terms of physical properties, so that the addition ratio of the melamine resin can be reduced, and the strength is maintained. The cost can be reduced.

【図面の簡単な説明】[Brief description of the drawings]

【図1】 尿素樹脂/メラミン樹脂の混合比率と硬化時
間の関係を示す図である。
FIG. 1 is a diagram showing the relationship between the mixing ratio of urea resin / melamine resin and the curing time.

【図2】 現行メラミン尿素樹脂と尿素樹脂とのブレン
ド比による常態曲げ強度の比較を示す図である。
FIG. 2 is a graph showing a comparison of normal bending strength according to a blend ratio of a current melamine urea resin and a urea resin.

【図3】 新規メラミン尿素樹脂と尿素樹脂とのブレン
ド比による常態曲げ強度の比較を示す図である。
FIG. 3 is a graph showing a comparison of a normal bending strength according to a blend ratio of a novel melamine urea resin and a urea resin.

【図4】 現行及び新規メラミン尿素樹脂使用による残
存率の比較を示す図である。
FIG. 4 is a diagram showing a comparison of the residual ratio between a current melamine urea resin and a new melamine urea resin.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】尿素樹脂と、ホルムアルデヒド:メラミ
ン:尿素:メタノールのモル比が(2.2〜6.0):
(1):(0.1〜1.0):(0.05〜1.0) で
反応させて得られた液状メラミン尿素樹脂接着剤を、
8:2〜3:7の割合で混合して木質チップに添加し、
加熱圧締することを特徴とするパーティクルボードの製
造方法。
1. A urea resin having a formaldehyde: melamine: urea: methanol molar ratio of (2.2 to 6.0):
(1): The liquid melamine urea resin adhesive obtained by reacting with (0.1-1.0) :( 0.05-1.0)
Mix at a ratio of 8: 2 to 3: 7 and add to the wood chips,
A method for producing a particle board, comprising heating and pressing.
JP32297997A 1997-11-25 1997-11-25 Production of particle board Pending JPH11156820A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP32297997A JPH11156820A (en) 1997-11-25 1997-11-25 Production of particle board

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP32297997A JPH11156820A (en) 1997-11-25 1997-11-25 Production of particle board

Publications (1)

Publication Number Publication Date
JPH11156820A true JPH11156820A (en) 1999-06-15

Family

ID=18149794

Family Applications (1)

Application Number Title Priority Date Filing Date
JP32297997A Pending JPH11156820A (en) 1997-11-25 1997-11-25 Production of particle board

Country Status (1)

Country Link
JP (1) JPH11156820A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115820178A (en) * 2022-12-20 2023-03-21 巴中建丰新材料有限公司 Glue for F4 star-grade shaving board, shaving board and preparation method of shaving board

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115820178A (en) * 2022-12-20 2023-03-21 巴中建丰新材料有限公司 Glue for F4 star-grade shaving board, shaving board and preparation method of shaving board

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