JPH03281202A - Preparation of particle board - Google Patents
Preparation of particle boardInfo
- Publication number
- JPH03281202A JPH03281202A JP8103890A JP8103890A JPH03281202A JP H03281202 A JPH03281202 A JP H03281202A JP 8103890 A JP8103890 A JP 8103890A JP 8103890 A JP8103890 A JP 8103890A JP H03281202 A JPH03281202 A JP H03281202A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- urea
- amino resin
- core layer
- parts
- 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.)
- Granted
Links
Landscapes
- Dry Formation Of Fiberboard And The Like (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、アミノ樹脂を用いて製造されるパティクルボ
ートの製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a method for manufacturing a particle boat manufactured using an amino resin.
さらに詳しくは、生産性向上をLI的とし、熱圧時間短
縮可能な、71液型アミノ樹脂を用いて製造されるパー
ティクルボーFの製造方法に関する。More specifically, the present invention relates to a method for producing Particle Bo F using a 71-liquid amino resin that improves productivity and shortens heat-pressing time.
従来、パーティクルボー )は、多層配合してなるパー
ティクルボードの多層におiJる、配合された樹脂の硬
化時間は、同一樹脂の配合成分の割合や硬化剤の添加量
等を変えることによって調製されている。Conventionally, the curing time of the compounded resins in the multilayer particle board is adjusted by changing the proportion of the compounded components of the same resin, the amount of curing agent added, etc. ing.
例えば3層パーティクルボードの表裏層部の木材質チッ
プのアミノ樹脂の配合は、直接熱盤に接するために熱劣
化を防止する目的で硬化剤を無添加にしたり、更には、
アルカリ触媒や有機アミノ触媒を添加し、硬化時間の遅
延を行ない熱劣化の防止を行なっていた。For example, when blending the amino resin in the wood chips on the front and back layers of a three-layer particle board, no curing agent is added in order to prevent thermal deterioration since the wood chips are in direct contact with the heating plate.
Alkali catalysts and organic amino catalysts have been added to delay curing time and prevent thermal deterioration.
また、芯層配合は表裏層部に反して伝熱速度が遅く、伝
熱時間の遅延を補うために硬化剤添加量を硬化促進させ
る最大量を配合して表裏層部との硬化速度の調整を行な
っていた。In addition, the heat transfer rate of the core layer is slower than that of the front and back layers, so in order to compensate for the delay in heat transfer time, the curing speed with the front and back layers is adjusted by adding the maximum amount of curing agent that will accelerate curing. was doing.
このように表裏層部と芯層部の木材質チップのアミノ樹
脂に同一樹脂を用い、配合成分によって硬化時間を調製
する方法では、年々ユーザーからの要望が高まるパーテ
ィクルホーl−の生産性向上に対処できなくなった。In this way, the method of using the same resin for the amino resin of the wood chips in the front and back layers and the core layer and adjusting the curing time depending on the blended components can improve the productivity of particle holes, which are becoming increasingly requested by users year by year. I couldn't cope anymore.
即ち、熱圧時間短縮を目的とし熱板温度を上昇させた場
合に表裏層部の熱劣化、芯層部の速硬化に対応出来ず目
的を果すことが困難であった。That is, when the temperature of the hot plate is raised for the purpose of shortening the hot pressing time, it is difficult to achieve the objective because it cannot cope with thermal deterioration of the front and back layer parts and rapid hardening of the core layer part.
本発明者は、このような問題を解決し、熱圧時間を短縮
し、生産性を大幅に向上せしめたものである。The present inventor has solved these problems, shortened the hot pressing time, and significantly improved productivity.
即ち、各々独自の特性をイリ与させた、二液型のアミノ
樹脂接着剤を、表裏層部及び芯層部に使い分けることで
表裏層部の熱劣化を防ぎ、なおかつ、芯層部の速硬化性
を有することを見出し、前記の問題を解決したものであ
る。In other words, by using two-component amino resin adhesives, each with unique properties, for the front and back layers and the core layer, thermal deterioration of the front and back layers can be prevented, and the core layer can harden quickly. The above-mentioned problem was solved.
〔課題を解決するだめの手段]
本発明者は上記状況に鑑み、従来行なわれていた一液型
樹脂を用いて、表裏層部及び芯層部の木材質チップに吹
き付は塗布せしむる方法では、もはや熱圧時間の短縮は
期待出来ないことが判った。[Means to Solve the Problem] In view of the above situation, the present inventors sprayed the wood chips on the front and back layers and the core layer using a conventional one-component resin. It was found that this method could no longer be expected to shorten the heat-pressing time.
かかる状況から本発明者らは、表裏層部用樹脂及び芯層
部用樹脂の二液型のアミン樹脂とし、各々に独自の特性
を付与させ、表裏層部の熱劣化を防ぎ、なおかつ、芯層
部に速硬化性をもたせ、熱圧時間短縮を可能ならしめる
二液型のアミノ樹脂としたものである。In view of this situation, the present inventors developed a two-component amine resin for the front and back layer parts and the core layer part, giving each of them unique characteristics, preventing thermal deterioration of the front and back layers, and still maintaining the core layer. It is a two-component amino resin that has quick curing properties in the layered parts and can shorten the heat-pressing time.
即ち、本発明は木材質チップをパーティクルボードの製
造に用いるに際し、表裏層部用及び芯層部用の木材質チ
ップの各々に、アミン樹脂を吹き付けながら攪拌・混合
し、均一に満遍なく塗布し、裏層部、芯層部及び表層部
の順序で順次積層し、積層体を得、該積層体を加熱・圧
縮し、パーティクルボードを製造する方法において、該
表裏層部用木材質チップに遅延硬化型のアミノ樹脂を、
芯層部用木材質チップに速硬化型のアミノ樹脂を用いる
パーティクルボードの製造方法であって、該遅延硬化型
アミノ樹脂の樹脂分が45〜5Qw t%であり、主成
分である尿素(U)とホルムアルデヒi′(F) ノモ
ル比(r’/U)が、 1.0〜1.5の尿素樹脂で、
該速硬化型アミノ樹脂の樹脂分が60〜70w t%で
あり、主成分である尿素(U)とホルムアルデヒド(F
)のモル比(F/11)が1.2〜2.0の尿素樹脂で
あることを特徴とするものである。さらに、遅延硬化型
アミノ樹脂および速硬化型のアミノ樹脂のメラミン(M
) とホルムアルデヒド(1’)のモル比(F/M )
が5.0〜20.0の尿素〜メラミン共縮合樹脂である
ことを特徴とするパーティクルボードの製造方法である
。That is, when using wood chips for the production of particle board, the present invention sprays amine resin on each of the wood chips for the front and back layers and the core layer while stirring and mixing, and applies the resin evenly and evenly. A method for producing particle board by sequentially laminating a back layer, a core layer, and a surface layer to obtain a laminate, and heating and compressing the laminate, wherein the wood chips for the front and back layers are delayed hardened. mold amino resin,
A method for producing a particle board using a fast-curing amino resin as a wood chip for the core layer, wherein the resin content of the slow-curing amino resin is 45 to 5 Qwt%, and the main component is urea (U). ) and formaldehyde i'(F) urea resin with a nomolar ratio (r'/U) of 1.0 to 1.5,
The resin content of the fast-curing amino resin is 60 to 70 wt%, and the main components are urea (U) and formaldehyde (F).
) is characterized by being a urea resin having a molar ratio (F/11) of 1.2 to 2.0. Furthermore, melamine (M
) and formaldehyde (1') molar ratio (F/M)
5.0 to 20.0 of the urea-melamine cocondensation resin.
本発明の詳細な説明する。The present invention will be described in detail.
本発明の遅延硬化型のアミノ樹脂接着剤は樹脂分45〜
604%(以下、wt%は単に%と記す)で主成分であ
る尿素(U)とホルムアルデヒド(F)のモル比(F/
U)が1.0〜1.5の尿素樹脂が用いられる。The delayed curing amino resin adhesive of the present invention has a resin content of 45 to
The molar ratio (F/
A urea resin having U) of 1.0 to 1.5 is used.
さらにメラミン(Vl’) とホルムアルデヒl”(
+’)のモル比(F/M)が5.0〜20.0の尿素−
メラミン共縮合樹脂が用いられることもある。In addition, melamine (Vl') and formaldehyde
+') molar ratio (F/M) of 5.0 to 20.0 -
Melamine cocondensation resins may also be used.
また、速硬化型のアミノ樹脂接着剤は樹脂分60〜70
wt%で主成分である尿素(ロ)とホルムアルデヒド(
F)のモル比(F/U)が1.2〜2.0の尿素樹脂が
用いられる。さらにメラミン(M)とホルムアルデヒド
(F)のモル比(P/M)が5.0〜20.0の尿素メ
ラミン共縮合樹脂が用いられることもある。In addition, fast-curing amino resin adhesives have a resin content of 60 to 70.
The main components are urea (b) and formaldehyde (wt%).
A urea resin having a molar ratio (F/U) of F) of 1.2 to 2.0 is used. Furthermore, a urea-melamine cocondensation resin having a molar ratio (P/M) of melamine (M) and formaldehyde (F) of 5.0 to 20.0 may be used.
積層体とは、表裏層部用及び芯層部用の木材質チップの
各々に、アミノ樹脂を吹き付けながら攪拌・混合し、均
一に満遍なく塗布し、裏層部、芯層部及び表層部の順序
で順送積層し、3層を形成(1、加熱・圧縮する1程に
移行するiスfのものをいつ。The laminate is made by spraying amino resin on each of the wood chips for the front and back layers and for the core layer, stirring and mixing them, applying them evenly and evenly, and then applying the amino resin to the wood chips for the front and back layers and the core layer in the order of the back layer, core layer, and surface layer. Laminate them progressively to form 3 layers (1. When to heat and compress the 1st step).
通常、パーう一イクルボー 1を製造する際に用いら才
jる接着剤は−・成型で、該接着剤の樹脂分は通常60
〜70%のものか使用される。これは同一の接rj剤を
用いて表裏層部及び芯層部の木材1jチツプに吹きイ」
けするアミノ樹脂として共有される。Usually, the adhesive used to manufacture Percycle Ball 1 is molded, and the resin content of the adhesive is usually 60%.
~70% is used. This is done by spraying the wood chips on the front and back layers and the core layer using the same glue.
It is commonly used as an amino resin for
、v、面部に吹付られた樹脂配合組成物はパーティクル
ボードの加熱成型時に犀!tJI硬化が求められ、また
、接着力が発現する以Ailに内部温度上昇により、発
生ずる蒸気圧による接着層の破壊(通常「バンク」と呼
ばれている)を防止するために配合組成物中の水分量を
極力城らし2、しかも吹き付は塗、l′1jiIJ能な
粘度と°する必要があり、通常60〜70%の樹脂分6
ごなるように設定されている。, v, The resin compound composition sprayed on the surface part is used during heat molding of particle board! tJI curing is required, and in order to prevent the adhesive layer from being destroyed (commonly called a "bank") due to the vapor pressure generated due to the internal temperature rise after the adhesive strength is developed, It is necessary to maintain the moisture content as much as possible, and also to maintain a viscosity that is suitable for spraying, and usually has a resin content of 60 to 70%.
It is set up to suit your needs.
従って、表裏層部用接着剤は同一樹脂分の接着剤を用い
加熱成型11.1の熱てノ9化防11,1と、芯層部−
・の〃)伝導の促進をト1的乙こ木+A質チップに塗?
−jざ杓たあとの全体の水分量(マント含水率と呼ばれ
ている)を芯層よりも高くする為に、 ・般に配合組成
物中の水分添加fitt多くする必要がある。Therefore, the adhesive for the front and back layer parts is the same resin content as the heat molding part 11.1 and the core layer part.
・No〃) Apply conduction promotion to To1 Otokogi + A quality chip?
In order to make the total water content after ladle (called mantle water content) higher than that of the core layer, it is generally necessary to increase the amount of water added to the blended composition.
年々高まりをみせている生産性向」二を目的とした熱圧
時間短縮の要望に応えるために、熱板温度の上昇、樹脂
接着剤の速硬化に対応するには同の樹脂接着剤では難し
くなってきているのは前述した通りである。In order to meet the demand for shortening heat pressing time with the aim of increasing productivity every year, it has become difficult for resin adhesives to respond to the rise in hot plate temperature and the rapid curing of resin adhesives. What is happening is as mentioned above.
本発明は表裏層部用については、樹脂分は45〜60%
であり、尿素(U)とホルムアルデヒl’(1’)のモ
ル比(F/U)が1.0〜1.5の尿素樹脂を用い、な
おかつ、メラミン01)とホルムアルデヒド(F)のモ
ル比(F/M)が50〜20,0の尿素−メラミン共縮
合樹脂を用いることが熱圧時間の遅延に効果があること
を見出した。In the present invention, for the front and back layers, the resin content is 45 to 60%.
Using a urea resin with a molar ratio (F/U) of urea (U) and formaldehyde l'(1') of 1.0 to 1.5, and a molar ratio of melamine 01) and formaldehyde (F) It has been found that using a urea-melamine cocondensation resin having an F/M ratio of 50 to 20.0 is effective in delaying the hot pressure time.
樹脂分45%以下でGJ表裏層部の熱硬化後の曲げ強度
、曲げヤング率、表面ヱIJ離強度他、諸物性の低下を
招き、また、60%以−ヒでは、硬化遅延効果が乏しく
好ましくない。特にパーティクルホー1−製造時の熱圧
温度が年々高くなりつつある現状下、熱劣化を防止する
には、60%以十の樹脂分接着剤では上記諸物性を満足
することは難しいことが判明し7だ6
本発明は樹脂分60%以七で製造された#Al1Fi接
着中にたた?iiζ2て水を)jI+え、樹脂分を表裏
16部用に45〜(i0%Qこ誹1整し7ても、目的と
する表裏層部用の遅延硬化型の樹脂を得ることl、Jで
きないことが判明した。こわの理由は定か−Cはないか
、同し縮合率(同号Y¥分1(i)で製造された45〜
60%樹脂接着剤とでは加熱 硬化■、−に於ける構造
か異なるためと考えらね【】。If the resin content is less than 45%, various physical properties such as the bending strength, bending Young's modulus, and surface IJ separation strength after thermosetting of the GJ front and back layers will decrease, and if it is more than 60%, the curing retardation effect will be poor. Undesirable. Particularly in the current situation where the heat pressure temperature during production of Particle Ho 1 is increasing year by year, it has been found that it is difficult to satisfy the above physical properties with an adhesive with a resin content of 60% or more in order to prevent thermal deterioration. 7.6 The present invention can be used to bond #Al1Fi manufactured with a resin content of 60% or more. ii ζ 2 and water) j I + E, and the resin content is 45 to 45 for the front and back 16 parts (i 0% It turned out that it could not be done.Is the reason for the stiffness certain?-Is there no C?The same condensation rate (45-
I don't think this is because the structure in heat curing is different for 60% resin adhesive.
さらに、熱目二時間の遅延を行な−)ために、モル比(
1・/IJ)をト−げる方策や配合時に尿素やメラミン
及びその他アルカ11金属塩、アミン類を添加づること
も硬化遅延としてこの機能を付与ずろことは出来るが、
何れも前記のパーう−イクルホー1物性の低下をきたし
2問題がある。In addition, a two-hour delay was carried out to increase the temperature of the molar ratio (
1/IJ) and the addition of urea, melamine, other alkali-11 metal salts, and amines at the time of formulation can also provide this function as curing retardation.
In either case, the above-mentioned per-cycle properties (1) deteriorate and there are (2) problems.
従って、パーティクルホーl物性の最適を求め、パー)
−イクルポー用・からの放出ポルJ−、ア月−)何二1
・を最適の条件にずろにはモル比(F/Ll)は1.0
〜1.5が々fましい6モル比が1.0以干ては曲げ強
度、曲げA・〉′グ率、表面711離強度−9の著しい
低重を招き、1.5以上ではパーティクルホー1からの
放出ホルムアルデヒドが日本農林規格のF−2規格(5
p四以下)を満足するご七が出来ないので好ましくない
。Therefore, we seek the optimum physical properties of particle holes, and par)
- For Ikurupo / Released from Pol J -, Azuki -) What 21
・The molar ratio (F/Ll) is 1.0 under the optimal conditions.
~ 1.5 If the molar ratio is too high, more than 1.0 will result in a significantly low bending strength, bending A・〉'g ratio, and surface 711 separation strength of -9, and if it is more than 1.5, particles will be generated. Formaldehyde released from Ho 1 meets the Japanese Agricultural Standards F-2 standard (5
This is not desirable because it is impossible to create a model that satisfies the requirements (p4 or less).
また、メラミン粉末の添加は硬化遅延にかなりの効果が
あるものの、水への溶解性が悪いために配合組成物中で
沈殿を起ごず恐れがあるので好ましくない。さらに、ア
ルカリ金属塩はアンダキュア(未硬化)を招き易く可使
時間の調整が11常に難しい。Further, although the addition of melamine powder has a considerable effect on curing delay, it is not preferable because it has poor solubility in water and may not precipitate in the blended composition. Furthermore, alkali metal salts tend to cause undercuring, making it difficult to adjust pot life.
パーティクルホーISには多くの場合、耐水性が要求さ
れる。該耐水1づを保持するためtこはメラミンとホル
ムアルデヒドのモル比(F/M)が15.0〜20.0
のモル比が好まり、<、5.0モル以下では上記諸物性
の性能低Jをきたし、20.0モル以十では経済的に不
利になるので好ましくない。Particle Ho IS is often required to be water resistant. In order to maintain the water resistance, the molar ratio (F/M) of melamine and formaldehyde is 15.0 to 20.0.
A molar ratio of less than 5.0 moles results in poor performance of the above-mentioned physical properties, and a molar ratio of more than 20.0 moles is not preferred because it is economically disadvantageous.
芯層部用樹脂接着剤は速硬化性を付+ノさ−iJるため
にモル比(F / 11 )は1.2〜2.0が好まし
く、さら乙こ好ましくは1.3〜1.6である。1.2
以Fではバケイクルボ−1・のIVみ1m/I11に対
する熱圧11.5間を0
15秒以下にすることが出来ない。また、2.0以上で
はパーティクルボードの放出ホルムアルデヒドがF−2
規格に満足することが困難である。The resin adhesive for the core layer portion preferably has a molar ratio (F/11) of 1.2 to 2.0, more preferably 1.3 to 1.0, in order to provide fast curing properties. It is 6. 1.2
In the following F, it is not possible to make the thermal pressure 11.5 seconds or less for the IV diameter 1 m/I11 of the Bakkeikurubo-1. In addition, if the particle board is over 2.0, the formaldehyde released by the particle board is F-2.
It is difficult to meet standards.
芯層周部樹脂分については、60〜70%が好ましく、
60%以下では、配合組成中の水分比率が高くなり、バ
ンクと呼ばれる芯層部からの層破壊が生じ易くなり好ま
しくない。また、70%以上では諸物性を保持しうるア
ミノ樹脂の縮合率からのて吹(=J可能な樹脂粘度に管
理することが出来ないので好ましくない。The resin content of the peripheral portion of the core layer is preferably 60 to 70%,
If it is less than 60%, the water content in the composition becomes high, and layer destruction from the core layer portion called a bank tends to occur, which is not preferable. Moreover, if it is 70% or more, it is not preferable because the resin viscosity cannot be controlled to a level that is higher than the condensation rate of the amino resin that can maintain various physical properties.
本発明における接着剤は、メラミンとの共縮合は耐水性
、中核剥離強度の物性面で有利である。Co-condensation of the adhesive with melamine in the present invention is advantageous in terms of physical properties such as water resistance and core peel strength.
ホルムアルデヒド(F)とメラミン(M)のモル比(F
/門)は5.0〜20.0が好ましく、さらに好ましく
は、10.0〜15.0である。5.0以下では耐水性
能低下をきたし、20,0以上では硬化速度を遅らす働
きがあるためにアンダーキュアーによる強度低下をきた
す恐れがあるので好ましくない。Molar ratio of formaldehyde (F) and melamine (M) (F
/gate) is preferably 5.0 to 20.0, more preferably 10.0 to 15.0. If it is less than 5.0, the water resistance performance will deteriorate, and if it is more than 20.0, it will slow down the curing speed, which may lead to a decrease in strength due to undercuring, which is not preferable.
以下実施例により本発明の詳細な説明する。 The present invention will be explained in detail below with reference to Examples.
1
実施例1
ホルムアルデヒド(lリ と尿素(U) とメラミン(
M)のモル比がI:0.8:0.05で樹脂分55%の
尿素−メラミン共縮合樹脂接着剤100部にワックスエ
マルジョン(固型分40%)1部を添加混合した後、水
3部を加えて接着剤組成物を得た。1 Example 1 Formaldehyde (L), urea (U) and melamine (
After adding and mixing 1 part of wax emulsion (solid content 40%) to 100 parts of a urea-melamine cocondensation resin adhesive with a molar ratio of I:0.8:0.05 and a resin content of 55%, water 3 parts were added to obtain an adhesive composition.
この接着剤組成物を木材質チップ(含水率3.0%)1
00部に対し13部吹き付け、塗付して表裏層部用チッ
プを得た。This adhesive composition was applied to wood chips (moisture content 3.0%) 1
A chip for the front and back layers was obtained by spraying and coating 13 parts to 00 parts.
同様にホルムアルデヒド(F) と尿素(11)とメラ
ミン(M)のモル比がI:0.75:0.旧で樹脂分6
5%の尿素−メラミン共縮合樹脂接着剤100部にワッ
クスエマルジョン(固型分40%)2部及び塩化アンモ
ニウム1部及び25%アンモニア水0.5部を加えた芯
層部用接着剤組成物を木材質アンダ(含水率7.0%)
100部に対し8部吹き付は塗付し芯層部用チップを得
た。Similarly, the molar ratio of formaldehyde (F), urea (11) and melamine (M) is I:0.75:0. Old resin content 6
Adhesive composition for the core layer part prepared by adding 2 parts of wax emulsion (solid content 40%), 1 part of ammonium chloride, and 0.5 part of 25% aqueous ammonia to 100 parts of a 5% urea-melamine cocondensation resin adhesive. Wood underlay (moisture content 7.0%)
A core layer chip was obtained by spraying 8 parts to 100 parts.
以」二のようにして得た表裏層部用チップと芯層部用チ
ップを交互に積層して三層構造のマツ1〜に構成した後
、ホットプレスを用い温度170°C1圧2
力30kg/ cnlで3分間圧縮し、厚さ15mmの
パーティクルボードを製造した。このパーティクルボー
ドの諸物性試験結果を第1表に示した。The chips for the front and back layers and the chips for the core layer obtained as described above were laminated alternately to form a three-layer structure of pine 1, and then a hot press was used at a temperature of 170°C, a pressure of 2, and a force of 30 kg. / cnl for 3 minutes to produce particle board with a thickness of 15 mm. Table 1 shows the results of various physical property tests of this particle board.
実施例2
ホルムアルデヒド(F) と尿素(U) とメラミン(
M)のモル比が]:0.7:0.01で樹脂分52%の
尿素−メラミン共縮合樹脂接着剤100部にワックスエ
マルジョン(固型分40%)1部を添加混合した後、水
1部を加えて接着剤組成物を得た。Example 2 Formaldehyde (F), urea (U) and melamine (
After adding and mixing 1 part of wax emulsion (solid content 40%) to 100 parts of a urea-melamine cocondensation resin adhesive with a resin content of 52% and a molar ratio of M) of ]:0.7:0.01, water was added. 1 part was added to obtain an adhesive composition.
この接着剤組成物を本材質チップ(含水率2.5%)1
00部に対し13部塗付して表裏層部用チップを得た。This adhesive composition was applied to this material chip (moisture content 2.5%) 1
A chip for the front and back layers was obtained by applying 13 parts to 00 parts.
同様にホルムアルデヒド(F)と尿素(U)とメラミン
(M)のモル比が1:0.7:0.03で樹脂分65%
の尿素−メラミン共縮合樹脂接着剤100部にワックス
エマルジョン(固型分40%)2部及び塩化アンモニウ
ム2部を加えた芯層部用接着剤組成物を木材質チップ(
含水率5.0%)100部に対し8部吹付塗付し芯層部
用チップを得た。Similarly, the molar ratio of formaldehyde (F), urea (U), and melamine (M) is 1:0.7:0.03, and the resin content is 65%.
A core layer adhesive composition prepared by adding 2 parts of wax emulsion (solid content 40%) and 2 parts of ammonium chloride to 100 parts of the urea-melamine cocondensation resin adhesive was mixed with wood chips (
A core layer chip was obtained by spraying 8 parts to 100 parts (water content: 5.0%).
このチップを用いて実施例1と同様な方法で厚3 さ1.5mmのパーティクルボードを得た。Using this chip, a thickness of 3 A particle board with a diameter of 1.5 mm was obtained.
このパーティクルボードの諸物性試験結果を第1表に示
した。Table 1 shows the results of various physical property tests of this particle board.
実施例3
ホルムアルデヒド(+’)と尿素(U)とメラミン(M
)のモル比が1.:0.85:0.05で樹脂分58%
の尿素−メラミン共縮合樹脂接着剤100部にワックス
エマルジョン(固型分40%)1部を添加・混合した後
、水5部を加えて接着剤組成物を得た。Example 3 Formaldehyde (+'), urea (U) and melamine (M
) has a molar ratio of 1. :0.85:0.05, resin content 58%
After adding and mixing 1 part of wax emulsion (solid content 40%) to 100 parts of the urea-melamine cocondensation resin adhesive, 5 parts of water was added to obtain an adhesive composition.
この接着剤組成物を木材質チップ(含水率3.5%)1
00部に対し13部吹付塗付して表層用アンダを得た。This adhesive composition was applied to wood chips (water content 3.5%) 1
A surface layer underlayer was obtained by spraying 13 parts to 00 parts.
同様に実施例1に準じて芯層部用チップを得た。Similarly, a core layer chip was obtained according to Example 1.
このチップを用いて表裏層部用チップと芯層部用チップ
を交互に積層して三層構造のマットに構成した後、ホッ
トプレスを用い温度170°C1圧力30kg/ c+
flで3分間圧縮し厚さ15mmのパーティクルボドを
製造した。このパーティクルボードの諸物性試験結果を
第1表に示した。Using this chip, chips for the front and back layers and chips for the core layer were alternately laminated to form a three-layered mat, and then hot pressed at a temperature of 170°C and a pressure of 30kg/c+.
A particle board having a thickness of 15 mm was produced by compressing it for 3 minutes using fl. Table 1 shows the results of various physical property tests of this particle board.
比較例1
4
)1部脂分6501′lのし’Q 3< tAf脂接着
剤10Q部にリンラス−1ン、′J1・・−3ン(固ヤ
1分・10%)1部添加混合し7た後7にε(部を加え
て接着剤組成物を得た。Comparative Example 1 4) 1 part fat content 6501'l, 'Q 3 < tAf fat adhesive 10Q part, 1 part Rin Las-1, 'J1...-3 N (hard resin 1 min, 10%) added and mixed After 7 hours, ε (parts) was added to 7 to obtain an adhesive composition.
′の接ri /f’l N口成物を木月質ナツプ(含水
率3.50<)+、oo部に灯し133部吹1J塗付し
、て表裏層部用チップ4+ iニー1だ。Apply 133 parts of N mouth composition to Kizuki nap (moisture content 3.50 <) + 0 part, spray 1J, and apply 1J of 133 parts, and then apply 1J of 133 parts to the front and back layers of chip 4 + i knee 1. is.
同I・Lに樹脂分65%の尿素樹脂接着剤100部に対
し、塩化−?ン千ニウj、1部及び25%アンモニア水
0.5部を和えた芯層部用接着剤を木材j1チ・プ(含
水’4: 7.0%) 100部Qこ対し8部吹きイt
jt 塗伺(−1疋、面部用十・ブを得た。In the same I/L, chloride -? Spray 8 parts of adhesive for the core layer mixed with 1 part of 1,000 ml of wood and 0.5 parts of 25% ammonia water to 100 parts of 100 parts of wood (water content: 7.0%). t
jt Nurikin (-1 hiki, I got 10 bu for the face part.
以1の様にし7て得た表裏層部用チップと芯層部用手・
・プを交7Tに積層して[−層構造の751に構成りま
た俊、ホノ1へプレスを用い温度150 ’C1圧力3
0kg/+(dで、i分[1旧下縮したものと、温度1
70°C1圧カニ(OkIN7’ (・品で3分間圧縮
し7たものの2種類の各+719さ15mm+2) ・
< 、−う−イクルボ−1を製1jM u ry。The chips for the front and back layers and the chips for the core layer obtained in step 7 as described in 1.
・Layer the layers in a 7T cross layer to form a layered structure of 751.
0 kg/+ (at d, i min [1 previous shrinkage and temperature 1
70°C 1 pressure crab (OkIN7' (2 types of crabs compressed for 3 minutes and 7 times + 719 x 15mm + 2)
< 1jMury produced - U-Ikurubo-1.
このバーデイクルJζ−1の1渚物性試験結果全第1
表01=jくし た。This Verdykle Jζ-1's physical property test results are the first in all.
Table 01 = j kushita.
比較例2
ボルムアルデヒ1(F) と尿素([+)とメラミン(
M)のモル比が1:0.75:0.旧で樹脂分65%の
尿素−メラミン共縮合樹脂接着剤100部にワンクスエ
マルン」ン(固型分40%)1部を添加混合した後、水
8部を加えて接着剤組成物を得た。Comparative Example 2 Bormaldehy 1 (F), urea ([+) and melamine (
The molar ratio of M) is 1:0.75:0. After adding and mixing 1 part of Wanx Emulsion (solid content 40%) to 100 parts of a urea-melamine cocondensation resin adhesive with a resin content of 65%, 8 parts of water was added to obtain an adhesive composition.
この接着剤組成物を木4.(質チップ(含水率3.5%
)100部に対し13部吹イク]塗(=t シて表裏層
部用千ノブを得た。。4. Apply this adhesive composition to wood. (Quality chips (moisture content 3.5%)
) 13 parts per 100 parts] coated (=t) to obtain 1,000 knobs for the front and back layers.
同様に樹脂分65%の尿素樹脂接着剤100部に対し塩
化アンモニウム1部及び25%アンモニア水0.5部を
加えた芯層部用接着剤を木材竹子ノブ(含水率7.0%
)100部に対し8部吹き付LJ塗イ・1し芯層部用デ
ツプを得た。Similarly, a core layer adhesive prepared by adding 1 part of ammonium chloride and 0.5 parts of 25% ammonia water to 100 parts of a urea resin adhesive with a resin content of 65% was applied to a wood bamboo knob (water content 7.0%).
) Sprayed 8 parts to 100 parts LJ coating A.1 to obtain a core layer depth.
該本材質チップを用いて比較例1と同様の条件乙こてパ
ーティクルボードを製造した。A trowel particle board was manufactured under the same conditions as in Comparative Example 1 using the chips made of this material.
7
弔
表
17−
〔発明の効果〕
本発明は、前記した様に多層パーティクルボーj・の製
造に際し、表裏層部用に遅延硬化型のアミノ樹脂接着剤
を、芯層部用に速硬化型のアミン樹脂接着剤を配合し、
吹き付け’124し、使用するという従来の装造方法に
何ら変わることのない節jJiな方法で、各々アミノ樹
脂接着剤に独自の特性を付与させ、二液型樹脂接着剤を
使用するという特徴を有するものである。7 Condolence Table 17 - [Effects of the Invention] As described above, the present invention, when producing a multilayer particle board, uses a slow-curing amino resin adhesive for the front and back layers and a fast-curing amino resin adhesive for the core layer. Contains amine resin adhesive of
Using a simple method that does not change in any way from the traditional installation method of spraying and using, each amino resin adhesive has unique characteristics, and the characteristic of using a two-component resin adhesive is that It is something that you have.
従来、問題であったパーティクルボー)の表裏層部の木
材質チ・ンブの熱板による劣化で)変質を接着剤の特性
により防止出来るのである。The properties of the adhesive can prevent deterioration of the wood-based chimney on the front and back layers of Particleboard, which has been a problem in the past due to the deterioration caused by the hot plate.
従って、接着強度他諸物性の低下もなく、熱圧時間が短
縮できるために生産性を著しく向トさ−けることが出来
るので、パーティクルボーF業界に与える、効果は犬な
るもなかある。Therefore, there is no decrease in adhesive strength or other physical properties, and the hot pressing time can be shortened, resulting in a significant increase in productivity, so the effects on the particle bow F industry are immense.
Claims (1)
に際し、表裏層部用及び芯層部用の木材質チップの各々
に、アミノ樹脂を吹き付けながら撹拌・混合し、均一に
満遍なく塗布し、裏層部、芯層部及び表層部の順序で順
次積層し、積層体を得、該積層体を加熱・圧縮し、パー
ティクルボードを製造する方法において、該表裏層部用
木材質チップに遅延硬化型のアミノ樹脂を、芯層部用木
材質チップに速硬化型のアミノ樹脂を用いるパーティク
ルボードの製造方法。 2)遅延硬化型アミノ樹脂の樹脂分が45〜60wt%
であり、主成分である尿素(U)とホルムアルデヒド(
F)のモル比(F/U)が、1.0〜1.5の尿素樹脂
である特許請求の範囲第1項記載のパーティクルボード
の製造方法。 3)速硬化型アミノ樹脂の樹脂分が60〜70wt%で
あり、主成分である尿素(U)とホルムアルデヒド(F
)のモル比(F/U)が1.2〜2.0の尿素樹脂であ
る特許請求の範囲第1項記載のパーティクルボードの製
造方法。 4)遅延硬化型アミノ樹脂および速硬化型のアミノ樹脂
のメラミン(M)とホルムアルデヒド(F)のモル比(
F/M)が5.0〜20.0の尿素−メラミン共縮合樹
脂である特許請求の範囲第1項〜第3項記載のパーティ
クルボードの製造方法。[Claims] 1) When wood chips are used to manufacture particle board, amino resin is sprayed on each of the wood chips for the front and back layers and the core layer while stirring and mixing, so that the wood chips are uniformly and evenly distributed. A method of manufacturing particle board by coating the particle board, sequentially laminating the back layer, core layer and surface layer to obtain a laminate, and heating and compressing the laminate, the wood chips for the front and back layers. A method for manufacturing particle board using a slow-curing amino resin for the core layer and a fast-curing amino resin for the wood chips for the core layer. 2) Resin content of delayed curing amino resin is 45 to 60 wt%
The main components are urea (U) and formaldehyde (
The method for producing particle board according to claim 1, wherein the urea resin has a molar ratio (F/U) of F) of 1.0 to 1.5. 3) The resin content of the fast-curing amino resin is 60 to 70 wt%, and the main components are urea (U) and formaldehyde (F).
2. The method for producing particle board according to claim 1, wherein the urea resin has a molar ratio (F/U) of 1.2 to 2.0. 4) Molar ratio of melamine (M) and formaldehyde (F) in slow-curing amino resin and fast-curing amino resin (
The method for producing particle board according to claims 1 to 3, wherein the urea-melamine cocondensation resin has a F/M) of 5.0 to 20.0.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2081038A JPH0716927B2 (en) | 1990-03-30 | 1990-03-30 | Particle board manufacturing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2081038A JPH0716927B2 (en) | 1990-03-30 | 1990-03-30 | Particle board manufacturing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03281202A true JPH03281202A (en) | 1991-12-11 |
| JPH0716927B2 JPH0716927B2 (en) | 1995-03-01 |
Family
ID=13735281
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2081038A Expired - Lifetime JPH0716927B2 (en) | 1990-03-30 | 1990-03-30 | Particle board manufacturing method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0716927B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6368528B1 (en) * | 1998-10-30 | 2002-04-09 | Masonite Corporation | Method of making molded composite articles |
| KR102298779B1 (en) * | 2020-03-03 | 2021-09-07 | 대한민국 | Wood fiber insulation with multilayer structure |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57152944A (en) * | 1981-03-18 | 1982-09-21 | Sanyo Kokusaku Pulp Co | Manufacture of dry type molded board |
| JPS5925656A (en) * | 1982-07-30 | 1984-02-09 | House Food Ind Co Ltd | Preparation of roux |
| JPS6124183A (en) * | 1984-07-12 | 1986-02-01 | 富士ゼロックス株式会社 | Corotron discharger |
-
1990
- 1990-03-30 JP JP2081038A patent/JPH0716927B2/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57152944A (en) * | 1981-03-18 | 1982-09-21 | Sanyo Kokusaku Pulp Co | Manufacture of dry type molded board |
| JPS5925656A (en) * | 1982-07-30 | 1984-02-09 | House Food Ind Co Ltd | Preparation of roux |
| JPS6124183A (en) * | 1984-07-12 | 1986-02-01 | 富士ゼロックス株式会社 | Corotron discharger |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6368528B1 (en) * | 1998-10-30 | 2002-04-09 | Masonite Corporation | Method of making molded composite articles |
| KR102298779B1 (en) * | 2020-03-03 | 2021-09-07 | 대한민국 | Wood fiber insulation with multilayer structure |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0716927B2 (en) | 1995-03-01 |
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