JPH10120747A - Woody fiber board and its production - Google Patents
Woody fiber board and its productionInfo
- Publication number
- JPH10120747A JPH10120747A JP27613096A JP27613096A JPH10120747A JP H10120747 A JPH10120747 A JP H10120747A JP 27613096 A JP27613096 A JP 27613096A JP 27613096 A JP27613096 A JP 27613096A JP H10120747 A JPH10120747 A JP H10120747A
- Authority
- JP
- Japan
- Prior art keywords
- formaldehyde
- fiber board
- wood fiber
- wood
- woody fiber
- 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
Links
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、フェノール類樹脂
を用いて製造する、木質繊維板およびその製造方法に関
する。さらに詳しくは、板状、片状、繊維状、粉状の木
質繊維をバインダーで接着し板状に成型した物であっ
て、多層から構成された木質繊維板で、かつ耐水性良好
で、木質繊維板からの放出ホルマリン量の極めて少ない
木質繊維板およびその製造方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a wood fiberboard produced using a phenolic resin and a method for producing the same. More specifically, it is a plate-like, flake-like, fibrous, powdery wood fiber bonded to a binder and molded into a plate shape, and is a wood fiber board composed of multiple layers, and has good water resistance, and The present invention relates to a wood fiberboard that emits very little formalin from a fiberboard and a method for producing the same.
【0002】[0002]
【従来の技術】従来、これら木質繊維板を接着成型する
場合、耐水性を有する木質繊維板を得るために、フェノ
ール樹脂等のホルムアルデヒド系樹脂等が主に用いられ
ている。2. Description of the Related Art Conventionally, when these wood fiber boards are bonded and formed, a formaldehyde resin such as a phenol resin is mainly used to obtain a water-resistant wood fiber board.
【0003】しかしホルムアルデヒド系樹脂を用いた木
質繊維板は、原料の一部にホルムアルデヒドが使われて
おり、熱圧による硬化時に未反応のホルムアルデヒドが
木質繊維板の中に残留するほか、硬化物も加水分解や縮
合反応の進行によってホルムアルデヒドを遊離する。こ
れらのホルムアルデヒドが木質繊維板の表面へ移動し板
面や側面から放出することになる。これがいわゆるホル
マリン臭で、刺激と不快感をもたらす原因となってい
る。これらホルムアルデヒドの問題点を解消するため
に、樹脂のホルムアルデヒド低減対策は種々検討されて
いる。[0003] However, wood fiberboard using formaldehyde resin uses formaldehyde as a part of the raw material, and unreacted formaldehyde remains in the wood fiberboard when cured by heat and pressure. Formaldehyde is released by the progress of hydrolysis and condensation reaction. These formaldehyde move to the surface of the wood fiber board and are released from the board surface and side surfaces. This is the so-called formalin odor, which causes irritation and discomfort. In order to solve these problems of formaldehyde, various measures for reducing formaldehyde in resins have been studied.
【0004】しかしながら、放出ホルムアルデヒドと耐
水性などの性能面とのバランスが取りにくく完全なもの
ではない。また、合板を通風のよい場所に保管し経日に
より拡散させる方法、成型後の木質繊維板表面にホルム
アルデヒドと反応し得る化合物を塗布する方法、アンモ
ニアガスチャンバー中で成型後の繊維板を処理する方法
等が提案されているが、後工程が複雑化し、ホルムアル
デヒド低減効果の持続性も不十分である。However, it is difficult to achieve a good balance between the formaldehyde emission and the performance such as water resistance, and it is not perfect. In addition, a method of storing plywood in a well-ventilated place and diffusing it over time, a method of applying a compound capable of reacting with formaldehyde to the surface of the molded wood fiber board, and treating the formed fiber board in an ammonia gas chamber Although methods and the like have been proposed, the post-process is complicated and the sustainability of the formaldehyde reduction effect is insufficient.
【0005】さらに、塗装仕上げをする方法等ホルムア
ルデヒドの放出量を減少させる方法が考えられるが実用
面において困難な場合もあるが、一時対処的であり根本
的な対処ではない。ゆえにホルムアルデヒドをまったく
含まないウレタン樹脂、水性ビニルウレタン樹脂等の使
用も考えられるが実用上汎用樹脂として使用することは
困難で大巾なコストアップになることは明らかである。[0005] Furthermore, a method of reducing the amount of formaldehyde emission such as a method of finishing the paint can be considered, but it is sometimes difficult in practical use, but it is a temporary measure and not a fundamental measure. Therefore, it is conceivable to use a urethane resin containing no formaldehyde at all, an aqueous vinyl urethane resin, or the like. However, it is obviously difficult to use it as a general-purpose resin in practice, and it will greatly increase the cost.
【0006】[0006]
【発明が解決しようとする課題】本発明は木質繊維板に
煩雑な処理を行うことなく、また、木質繊維板の諸強度
や耐水性を失うことなく、過酷な使用環境下にあって
も、極めて低い放散ホルムアルデヒド量の少ない木質繊
維板およびその製造方法を提供することにある。DISCLOSURE OF THE INVENTION The present invention does not require complicated treatment of a wood fiber board, does not lose various strengths and water resistance of the wood fiber board, and can be used in a severe use environment. It is an object of the present invention to provide a wood fiber board having a very low amount of emitted formaldehyde and a method for producing the same.
【0007】[0007]
【課題を解決するための手段】本発明者らは、これらの
課題を達成するために、鋭意検討した結果、多層構成の
木質繊維板において、特定組成のフェノール樹脂をバイ
ンダーとして用い、かつ木質繊維にホルムアルデヒドと
反応しうる捕捉剤を混合しすることにより、耐水性良好
で、過酷な条件下においても長期間放散ホルムアルデヒ
ド量を制御させうることを見出だすに至った。Means for Solving the Problems The present inventors have conducted intensive studies in order to achieve these objects, and as a result, using a phenolic resin having a specific composition as a binder in a multi-layered wood fiber board, It has been found that by mixing a scavenger which can react with formaldehyde into water, the water resistance is good and the amount of emitted formaldehyde can be controlled for a long period even under severe conditions.
【0008】すなわち、本発明はホルムアルデヒド
(F)とフェノール類(P)のモル比(F/P)が1.
0〜3.0であるフェノール樹脂と、木質繊維板の表裏
層部及び芯層部の全層又は何れかの層にホルムアルデヒ
ド捕捉剤を用いてなる耐水性良好、かつ放出ホルマリン
量の極めて少ない木質繊維板及び木質繊維にフェノール
樹脂を混合し、木質繊維板を製造する方法において、該
フェノール樹脂のホルムアルデヒド(F)とフェノール
類(P)のモル比(F/P)を1.0〜3.0に調製
し、木質繊維に混合し、該木質繊維板の表裏層部及び芯
層部の全層又は何れかの層の木質繊維にホルムアルデヒ
ド捕捉剤を該アミノ樹脂を混合する前または後に混合し
て、加圧、成形することを特徴とする耐水性良好、かつ
放出ホルマリン量の極めて少ない木質繊維板の製造方法
に関する。That is, in the present invention, the molar ratio (F / P) of formaldehyde (F) to phenols (P) is 1.
A phenolic resin of 0 to 3.0 and a woody material having good water resistance and a very small amount of released formalin by using a formaldehyde scavenger in all or any of the front and back layers and the core layer of the wood fiberboard In a method for producing a wood fiber board by mixing a phenol resin with a fiber board and wood fiber, the molar ratio (F / P) of formaldehyde (F) to phenols (P) of the phenol resin is 1.0 to 3. 0, mixed with wood fibers, and mixed with a formaldehyde scavenger before or after mixing the amino resin with wood fibers in all or any of the front and back layers and the core layer of the wood fiber board. The present invention also relates to a method for producing a wood fiber board having good water resistance and an extremely small amount of released formalin, characterized by being pressed and molded.
【0009】[0009]
【発明の実施の形態】以下に、本発明を詳細に説明す
る。本発明にいう木質繊維とは、木材や、禾本科、椰子
科等の茎等が列示できる。木質繊維を、板状、片状、繊
維状、粉状とし、接着剤により板状に成型したものを本
発明では木質繊維板と称し、厚み方向に多層に構成され
ているものを対象とする。DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below in detail. The wood fibers referred to in the present invention include wood, stems of Graminaceae, coconut family and the like. In the present invention, a wood fiber is formed into a plate shape, a piece shape, a fiber shape, a powder shape, and formed into a plate shape with an adhesive. .
【0010】本発明でのフェノール類樹脂とは、通常、
フェノール、レゾルシノール、クレゾール、キシレノー
ル、ビスフェノールA等のフェノール類一種若しくは二
種以上と、ホルムアルデヒド等のアルデヒド類とを反応
させたオリゴマーおよび/またはポリマーをいう。該フ
ェノール樹脂はホルムアルデヒドとフェノール類のモル
比(F/P)が1.0〜3.0である。モル比が1.0
未満ではホルムアルデヒド放散量低減という目的にはよ
り有利であるが、バインダーとして硬化させた場合、硬
化が遅いばかりか、硬化反応後三次元的な架橋構造をと
りにくく、硬化物の強度や耐水性が低くなり、ひいては
木質繊維板の生産性、強度、耐水性を失う可能性があ
る。また、3.0を超えると、もはや生産性、強度、耐
水性がより以上向上する可能性は低く、むしろホルムア
ルデヒド放散量増大が問題となりやすい。フェノール樹
脂は二種類以上のフェノール類を混合して用いてもよ
い。In the present invention, the phenolic resin is usually
An oligomer and / or polymer obtained by reacting one or more phenols such as phenol, resorcinol, cresol, xylenol, and bisphenol A with an aldehyde such as formaldehyde. The phenol resin has a molar ratio of formaldehyde to phenols (F / P) of 1.0 to 3.0. The molar ratio is 1.0
If it is less than the value, it is more advantageous for the purpose of reducing the amount of formaldehyde emission, but when it is cured as a binder, not only the curing is slow, but it is difficult to take a three-dimensional crosslinked structure after the curing reaction, and the strength and water resistance of the cured product are low. The wood fiberboard may lose its productivity, strength and water resistance. On the other hand, if it exceeds 3.0, it is unlikely that the productivity, strength and water resistance will be further improved, and the increase in the amount of formaldehyde emission tends to be a problem. The phenol resin may be a mixture of two or more phenols.
【0011】また、フェノール樹脂製造時種々の特性を
付与させるためポリビニルアルコール、セルロース誘導
体等他のポリマー類と混合してもよいし、使用に際し必
要に応じて、硬化剤、発水剤、難燃剤、防虫剤、防腐剤
等と混合使用してもよい。The phenolic resin may be mixed with other polymers such as polyvinyl alcohol and cellulose derivatives in order to impart various properties during the production of the phenolic resin. If necessary, a curing agent, a water-producing agent, a flame retardant, etc. , An insecticide, a preservative and the like.
【0012】また、本発明に用いるフェノール類樹脂の
製造方法や性状は、特に限定するものではなく、通常適
用される製造方法を用いてよい。フェノール類樹脂は、
多層で構成される木質繊維板のバインダーとして、表裏
層、芯層用として使用できる。該フェノール樹脂は触媒
の使用または、加熱により高分子化し部分的に架橋した
硬化物を形成し高硬度の接着層となるため得られる木質
繊維板の曲げ強度や剛性が高くなり望ましい。The production method and properties of the phenolic resin used in the present invention are not particularly limited, and a production method generally applied may be used. Phenolic resins are
As a binder for a wood fiber board composed of multiple layers, it can be used for the front and back layers and the core layer. The phenol resin is preferable because it uses a catalyst or forms a cured product which is polymerized by heating and partially crosslinked to form a high-hardness adhesive layer because the bending strength and rigidity of the obtained wood fiber board are increased.
【0013】本発明のホルムアルデヒドと反応しうる捕
捉剤とは、ホルムアルデヒドと反応する物質であれば、
特に限定するものではない。木質繊維板製造工程で、揮
散したり変質しホルムアルデヒドとの反応性を失うよう
なものは、ホルムアルデヒド低減機能が劣るため望まし
いものではない。また、ホルムアルデヒドとの反応速度
が遅いものも望ましいものではない。かかる観点から、
アンモニウム塩類、分子内にアミノ基、アミド基、イミ
ノ基を有する化合物、および/または亜硫酸塩または重
亜硫酸塩の一種または二種以上を用いることが望まし
い。The scavenger capable of reacting with formaldehyde of the present invention is a substance which reacts with formaldehyde.
There is no particular limitation. In the wood fiberboard manufacturing process, those which volatilize or deteriorate and lose their reactivity with formaldehyde are not desirable because of their poor formaldehyde reducing function. Further, those having a low reaction rate with formaldehyde are not desirable. From this perspective,
It is preferable to use one or more of ammonium salts, a compound having an amino group, an amide group, or an imino group in a molecule, and / or a sulfite or a bisulfite.
【0014】アンモニウム塩類としては、硝酸アンモニ
ウム、硫酸アンモニウム、塩酸アンモニウム、燐酸アン
モニウム、炭酸アンモニウム、酢酸アンモニム等が例示
できる。また、分子内にアミノ基、アミド基、イミノ基
を有する化合物としては、尿素、チオ尿素、メラミン、
ジシアンジアミド、ベンゾグアナミン等が例示できる。
さらに、亜硫酸塩または重亜硫酸塩としては、亜硫酸ナ
トリウム、亜硫酸水素ナトリウム、亜硫酸アンモニウ
ム、亜硫酸水素アンモニウム等が例示できる。Examples of the ammonium salts include ammonium nitrate, ammonium sulfate, ammonium hydrochloride, ammonium phosphate, ammonium carbonate, and ammonium acetate. Examples of the compound having an amino group, an amide group, and an imino group in the molecule include urea, thiourea, melamine,
Dicyandiamide, benzoguanamine and the like can be exemplified.
Furthermore, examples of the sulfite or bisulfite include sodium sulfite, sodium bisulfite, ammonium sulfite, and ammonium bisulfite.
【0015】これらの化合物は、表裏層あるいは、最内
層あるいは、表裏層、最内層の木質繊維に添加すること
ができる。ホルムアルデヒド捕捉剤の添加は、フェノー
ルを混合する前または後の何れに混合してもよい。ま
た、添加量は木質繊維のバインダーとして用いるフェノ
ール類樹脂の固形分に対し、5〜40重量%が好まし
く、更に好ましくは10〜30重量%が好適である。These compounds can be added to the front and back layers, the innermost layer, or the wood fibers of the front and back layers and the innermost layer. The addition of the formaldehyde scavenger may be added before or after mixing the phenol. The amount of addition is preferably 5 to 40% by weight, more preferably 10 to 30% by weight, based on the solid content of the phenolic resin used as the binder for the wood fiber.
【0016】[0016]
【実施例】以下、実施例を挙げて本発明を詳述するが、
本発明はこれら実施例に限定されるものではない。ま
た、部または%は特にことわりのない限り重量部または
重量%を表す。 実施例1 撹拌機、還流コンデンサー、および温度計を備えた反応
容器に、フェノール類としてフェノール636部、ホル
ムアルデヒドとしてパラホルムアルデヒド(ホルムアル
デヒド含有量80%)380部をいれ、触媒として濃度
48%苛性ソーダ水溶液150部と水100部を加え反
応温度80℃で2時間反応させた後、冷却しフェノール
樹脂を得た(以下A1と略す)。A1は、ホルムアルデ
ヒドとフェノールのモル比(F/P)は1.5であっ
た。また、不揮発分は50%に調製した。Hereinafter, the present invention will be described in detail with reference to Examples.
The present invention is not limited to these examples. Parts and% represent parts by weight or% by weight unless otherwise specified. Example 1 A reaction vessel equipped with a stirrer, a reflux condenser, and a thermometer was charged with 636 parts of phenol as phenol and 380 parts of paraformaldehyde (formaldehyde content of 80%) as formaldehyde. And 100 parts of water were added and reacted at a reaction temperature of 80 ° C. for 2 hours, and then cooled to obtain a phenol resin (hereinafter abbreviated as A1). For A1, the molar ratio of formaldehyde to phenol (F / P) was 1.5. The nonvolatile content was adjusted to 50%.
【0017】つぎに、A1を用い以下に示す方法、条件
で木質繊維板を作成した。木質繊維としてラワン剤をフ
レーカーで木片とし、水分4%まで乾燥した。つぎに、
目開き1mmの篩で篩分けし、篩下の物を表裏層用木質
繊維とし、篩上の物を芯層用木質繊維とした。つぎに、
準備したA1樹脂300部、50%ワックスエマルショ
ン10部、水50部を混合し、表裏層用木質繊維104
0部にスプレー塗布した。A1の絶乾燥木質繊維への吹
き付け率は15%となった。塗布後の木質繊維から45
0部ずつ分取し、表層、裏層用とした。つぎに、芯層用
木質繊維1040部、粉末尿素15部を均一に混合し芯
層用木質繊維とした。それに、準備したA1樹脂150
部、50%ワックスエマルション10部、水20部を混
合したものを芯層用木質繊維にスプレー塗布した。A1
の絶乾燥木質繊維への吹き付け率は7.5%となった。
また、粉末尿素の混合比率はA1固形分換算20%とな
った。塗布後の木質繊維から1100部採取し、芯層用
とした。つぎに、38cm角の枠内に裏層用木質繊維を
均一に塗布し、続けて芯層用、さらに表層用を散布し堆
積した繊維マットを、180℃の熱板に挟んで、30K
gf/cm2の圧力で6分間圧締し、厚み20mm、密
度750kg/m3の木質繊維板を得た。物性評価結果
を表1に示す。Next, a wood fiberboard was prepared using A1 under the following method and conditions. As a wood fiber, a lauan agent was made into a piece of wood using a flaker and dried to a moisture content of 4%. Next,
The mixture was sieved with a sieve having an opening of 1 mm, the material under the screen was used as the wood fibers for the front and back layers, and the material on the screen was used as the wood fibers for the core layer. Next,
300 parts of the prepared A1 resin, 10 parts of a 50% wax emulsion, and 50 parts of water were mixed, and the wood fibers 104 for the front and back layers were mixed.
0 parts were spray applied. The spraying rate of A1 on the absolutely dry wood fiber was 15%. 45 from wood fiber after application
0 parts were separated and used for the surface layer and the back layer. Next, 1040 parts of the core layer wood fiber and 15 parts of powdered urea were uniformly mixed to obtain a core layer wood fiber. In addition, prepared A1 resin 150
The mixture obtained by spraying 10 parts of a 50% wax emulsion and 20 parts of water was spray-coated on the wood fiber for the core layer. A1
Spray rate on the absolutely dry wood fiber was 7.5%.
The mixing ratio of the powdered urea was 20% in terms of A1 solid content. 1100 parts were collected from the wood fibers after application and used as a core layer. Next, the wood fiber for the back layer was uniformly applied in a frame of 38 cm square, and the fiber mat for the core layer and the surface layer was further sprayed and deposited.
It was pressed at a pressure of gf / cm 2 for 6 minutes to obtain a wood fiber board having a thickness of 20 mm and a density of 750 kg / m 3 . Table 1 shows the physical property evaluation results.
【0018】実施例2 フェノールを477部、48%苛性ソーダ水溶液を11
2部、水80部に変更した以外は、実施例1と同様にフ
ェノール樹脂を得た(以下A2と略す)。A2のモル比
(F/P)は2.0であった。また、不揮発分は50%
に調製し、実施例1と同様に木質繊維板を得た。物性評
価結果を表1に示す。Example 2 477 parts of phenol and 11% of 48% aqueous sodium hydroxide solution
A phenol resin was obtained in the same manner as in Example 1 except that the amount was changed to 2 parts and water to 80 parts (hereinafter abbreviated as A2). The molar ratio (F / P) of A2 was 2.0. Non-volatile content is 50%
And a wood fiber board was obtained in the same manner as in Example 1. Table 1 shows the physical property evaluation results.
【0019】実施例3 フェノール樹脂はA2を用い、表裏層用木質繊維104
0部、粉末尿素30部を均一に混合し、表裏層用木質繊
維とし芯層用木質繊維の粉末尿素を除いた以外は実施例
1と同様に木質繊維板を得た。物性評価結果を表1に示
す。Example 3 A2 is used as the phenol resin, and the wood fibers 104 for the front and back layers are used.
0 parts and 30 parts of powdered urea were uniformly mixed to obtain a wood fiber board in the same manner as in Example 1 except that the wood fiber for the front and back layers was used and the wood fiber for the core layer was not powdered urea. Table 1 shows the physical property evaluation results.
【0020】実施例4 フェノールを381部、48%苛性ソーダ水溶液を90
部、水60部に変更した以外は、実施例1と同様にフェ
ノール樹脂を得た(以下A3と略す)。A3のモル比
(F/P)は2.5であった。また、不揮発分は50%
に調製し、実施例1と同様に木質繊維板を得た。物性評
価結果を表1に示す。Example 4 381 parts of phenol and 90% of 48% aqueous sodium hydroxide solution
Phenolic resin was obtained in the same manner as in Example 1 except that the amount of phenolic resin was changed to 60 parts by weight (hereinafter abbreviated as A3). The molar ratio (F / P) of A3 was 2.5. Non-volatile content is 50%
And a wood fiber board was obtained in the same manner as in Example 1. Table 1 shows the physical property evaluation results.
【0021】比較例1 実施例1の粉末尿素15部を除いた以外は実施例1と同
様に行った。その物性評価結果を表2に示す。Comparative Example 1 The procedure of Example 1 was repeated except that 15 parts of the powdered urea were omitted. Table 2 shows the physical property evaluation results.
【0022】比較例2 実施例2の粉末尿素15部を除いた以外は実施例1と同
様に行った。その物性評価結果を表2に示す。Comparative Example 2 The procedure of Example 1 was repeated except that 15 parts of powdered urea were removed. Table 2 shows the physical property evaluation results.
【0023】比較例3 実施例4の粉末尿素15部を除いた以外は実施例1と同
様に行った。その物性評価結果を表2に示す。Comparative Example 3 The procedure of Example 1 was repeated except that 15 parts of powdered urea were removed. Table 2 shows the physical property evaluation results.
【0024】比較例4 フェノールを1059部、48%苛性ソーダ水溶液を9
0部、水200部に変更した以外は、実施例1と同様に
フェノール樹脂を得た(以下B1と略す)。B1のモル
比(F/P)は0.9であった。また、不揮発分は50
%に調製し、実施例1と同様に木質繊維板を得た。物性
評価結果を表2に示す。Comparative Example 4 1059 parts of phenol and 9% of 48% aqueous sodium hydroxide solution
A phenol resin was obtained in the same manner as in Example 1 except that the amount was changed to 0 parts and water was changed to 200 parts (hereinafter abbreviated as B1). The molar ratio (F / P) of B1 was 0.9. The non-volatile content is 50
%, And a wood fiberboard was obtained in the same manner as in Example 1. Table 2 shows the physical property evaluation results.
【0025】比較例5 フェノールを298部、48%苛性ソーダ水溶液を70
部、水40部に変更した以外は、実施例1と同様にフェ
ノール樹脂を得た(以下B2と略す)。B2のモル比
(F/P)は3.2であった。また、不揮発分は50%
に調製し、実施例1と同様に木質繊維板を得た。物性評
価結果を表2に示す。Comparative Example 5 298 parts of phenol and 70% of 48% aqueous sodium hydroxide solution
Phenol resin was obtained in the same manner as in Example 1 except that the amount was changed to 40 parts by weight and water was changed to 40 parts (hereinafter abbreviated as B2). The molar ratio (F / P) of B2 was 3.2. Non-volatile content is 50%
And a wood fiber board was obtained in the same manner as in Example 1. Table 2 shows the physical property evaluation results.
【0026】[0026]
【表1】 [Table 1]
【0027】[0027]
【表2】 [Table 2]
【0028】[0028]
【発明の効果】本発明では、従来技術では達成されなか
った、木質繊維板において、極めて過酷な使用条件にお
いても、特定組成のフェノール樹脂バインダーとホルム
アルデヒドと反応しうる捕捉剤を用いることにより、耐
水性良好で、過酷な条件下においても長期間放散ホルム
アルデヒド量を制御させうる、木質繊維板を得ることが
可能となった。According to the present invention, even in extremely severe use conditions, the use of a phenolic resin binder having a specific composition and a scavenger capable of reacting with formaldehyde in a wood fiberboard, which has not been achieved by the prior art, makes it possible to obtain a water-resistant material. It has become possible to obtain a wood fiber board which has good properties and can control the amount of formaldehyde emitted for a long period of time even under severe conditions.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 古藤 信彦 山口県下関市彦島迫町七丁目1番1号 三 井東圧化学株式会社内 ──────────────────────────────────────────────────の Continuing on the front page (72) Inventor Nobuhiko Koto 7-1-1, Hikoshimasako-cho, Shimonoseki-shi, Yamaguchi Pref.
Claims (4)
類(P)のモル比(F/P)が1.0〜3.0であるフ
ェノール樹脂と、木質繊維板の表裏層部及び芯層部の全
層又は何れかの層にホルムアルデヒド捕捉剤を用いてな
る耐水性良好、かつ放出ホルマリン量の極めて少ない木
質繊維板。1. A phenol resin having a molar ratio (F / P) of formaldehyde (F) to phenols (P) of from 1.0 to 3.0, and a total of front and back layers and a core layer of a wood fiber board. A wood fiber board which has good water resistance and a very small amount of released formalin, using a formaldehyde scavenger for one or any of the layers.
木質繊維板を製造する方法において、該フェノール樹脂
のホルムアルデヒド(F)とフェノール類(P)のモル
比(F/P)を1.0〜3.0に調製し、木質繊維に混
合し、該木質繊維板の表裏層部及び芯層部の全層又は何
れかの層の木質繊維にホルムアルデヒド捕捉剤を該アミ
ノ樹脂を混合する前または後に混合して、加圧、成形す
ることを特徴とする耐水性良好、かつ放出ホルマリン量
の極めて少ない木質繊維板の製造方法。2. A wood fiber mixed with a phenolic resin,
In the method for producing a wood fiber board, a molar ratio (F / P) of formaldehyde (F) and phenols (P) of the phenol resin is adjusted to 1.0 to 3.0, mixed with wood fiber, and mixed. A formaldehyde scavenger is mixed with or before and after mixing the amino resin with the wood fibers of all or any of the front and back layer portions and the core layer portion of the wood fiber board, followed by pressing and molding. A method for producing a wood fiber board having good water resistance and an extremely small amount of released formalin.
ム塩、アミノ基、アミド基、イミノ基を含む化合物およ
び/または亜硫酸塩類または重亜硫酸塩類の少なくとも
1種または2種以上からなる請求項2記載の木質繊維板
の製造方法。3. The wood fiber board according to claim 2, wherein the formaldehyde scavenger comprises at least one or more of ammonium salts, compounds containing an amino group, an amide group and an imino group and / or sulfites or bisulfites. Manufacturing method.
繊維板。4. The wood fiberboard produced in claim 2.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27613096A JPH10120747A (en) | 1996-10-18 | 1996-10-18 | Woody fiber board and its production |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27613096A JPH10120747A (en) | 1996-10-18 | 1996-10-18 | Woody fiber board and its production |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH10120747A true JPH10120747A (en) | 1998-05-12 |
Family
ID=17565213
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27613096A Pending JPH10120747A (en) | 1996-10-18 | 1996-10-18 | Woody fiber board and its production |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH10120747A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007204624A (en) * | 2006-02-02 | 2007-08-16 | Dainippon Ink & Chem Inc | Aqueous phenolic resin composition and binder |
-
1996
- 1996-10-18 JP JP27613096A patent/JPH10120747A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007204624A (en) * | 2006-02-02 | 2007-08-16 | Dainippon Ink & Chem Inc | Aqueous phenolic resin composition and binder |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4282119A (en) | Manufacture of chipboard having high strength and reduced formaldehyde emission, using a minor amount of protein in combination with low formaldehyde:urea resins | |
US4362827A (en) | Manufacture of chipboard | |
US5637658A (en) | Modified phenol-aldehyde resin and binder system | |
JP2007521163A (en) | Oriented strand board | |
JP2000280208A (en) | Wood fiber plate and its manufacture | |
CA2244667C (en) | Bonding agent composition, its use as well as a process for the production of particle board | |
JPH10119010A (en) | Wooden fiber board and manufacture thereof | |
CA1298942C (en) | Wood treatment composition and process | |
JPH1076505A (en) | Wooden fiber board and its manufacture | |
WO2003093339A1 (en) | Melamine-urea-formaldehyde resins modified with cyclic urea prepolymer and sodium metabisulfite | |
JPH10120747A (en) | Woody fiber board and its production | |
JP2001038707A (en) | Manufacture of wood fiberboard | |
EP0259442A1 (en) | Fire retardant composition | |
EP0915141B1 (en) | Phenol-melamine-urea-formaldehyde copolymer resin compositions, method of making and curing catalysts thereof | |
JP3979705B2 (en) | Manufacturing method of wooden board | |
JPH11172219A (en) | Wood fiberboard and its preparation | |
JP2000117708A (en) | Manufacture of woody board | |
JP2002127113A (en) | Wood fiber board and its manufacturing method | |
JP2000006117A (en) | Woody fiber board and its manufacture | |
JPH1180694A (en) | Resin composition | |
JPH10109381A (en) | Water-resisting lignocellulose board and manufacture thereof | |
JP3898320B2 (en) | Production method of wood | |
JPS5817547B2 (en) | Catalyst for amino resin polycondensation | |
JP2000280209A (en) | Woody fiberboard and manufacture thereof | |
JP2000001600A (en) | Wood fiber board and its production |