JPH10151608A - Manufacture of woody board - Google Patents

Manufacture of woody board

Info

Publication number
JPH10151608A
JPH10151608A JP32768196A JP32768196A JPH10151608A JP H10151608 A JPH10151608 A JP H10151608A JP 32768196 A JP32768196 A JP 32768196A JP 32768196 A JP32768196 A JP 32768196A JP H10151608 A JPH10151608 A JP H10151608A
Authority
JP
Japan
Prior art keywords
resin
adhesive
board
weight
pts
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.)
Withdrawn
Application number
JP32768196A
Other languages
Japanese (ja)
Inventor
Koji Higuchi
晃司 樋口
Michitaka Ikeyama
道高 池山
Yoshiharu Imanishi
恵施 今西
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.)
Eidai Co Ltd
Original Assignee
Eidai Co Ltd
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 Eidai Co Ltd filed Critical Eidai Co Ltd
Priority to JP32768196A priority Critical patent/JPH10151608A/en
Publication of JPH10151608A publication Critical patent/JPH10151608A/en
Withdrawn legal-status Critical Current

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  • Dry Formation Of Fiberboard And The Like (AREA)

Abstract

PROBLEM TO BE SOLVED: To improve the strength and water resistance of a woody board by preventing the precure of an adhesive from occurring during a process of manufacturing the woody board. SOLUTION: As a blending method, 3 pts.wt. of methanol, 2.5 pts.wt. of a resol resin having 40% of a resin content and 2.5 pts.wt. of an aqueous solution having 20% of ammonium chloride are addeted to 200 pts.wt. of a melamine resin adhesive having 50% of a resin content, and they are stirred. The above- mentioned adhesive thus prepared is applied to wet wood fibers at the rate of 15% of the resin in terms of solid content, and the wood fibers are allowed to pass through a flash dryer to be dried to a level of at most 20% of the moisture content. Then, the above-mentioned wood fibers are formed into a mat shape, and the formed mat is pressed for three minutes under the hot- pressing condition that a temperature is 200 deg.C and pressure is 25kgf/cm<2> , thereby manufacturing a medium-duty fiber board having 7mm in thickness.

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、パ−ティクルボ−
ドや中質繊維板、配向性ボ−ドなど木質ボ−ドの製造方
法に係る。
BACKGROUND OF THE INVENTION 1. Field of the Invention
The present invention relates to a method for producing a wooden board such as a board, a medium fiber board, and an oriented board.

【0002】[0002]

【従来の技術】尿素樹脂や尿素メラミン樹脂、メラミン
樹脂、メラミンフェノ−ル樹脂等、アミノ系樹脂を用い
る木質ボ−ド、例えば中質繊維板(略してMDF)やパ
−ティクルボ−ド(略してPB)、配向性ボ−ド(略し
てOSB)などは、製造工程中においてプレキュア(前
硬化)によって接着力が低下する恐れがある。
2. Description of the Related Art Wood boards using amino resins such as urea resins, urea melamine resins, melamine resins, melamine phenol resins, etc., such as medium fiberboard (MDF for short) and particle boards (abbreviated for short). PB), orienting boards (abbreviated to OSB), etc., may have a reduced adhesive strength due to pre-curing (pre-curing) during the manufacturing process.

【0003】例えば、PBの場合木材チップに上記樹脂
を塗布した後、マット状に積層して熱圧成形することに
なるが、フォ−ミングマットがホットプレスによって所
定の厚みに圧縮されるまで数十秒の時間を必要とするた
め、常に熱盤に接しているマット表面では表層用チップ
に塗布されている接着剤がプレキュアを起こしてその部
分の接着剤の流動性を悪化させ、その結果PB表面付近
の木材チップの接着力が弱くなるという欠点があった。
[0003] For example, in the case of PB, the above resin is applied to a wood chip, then laminated in a mat shape and subjected to hot-press molding. However, it takes several hours until the forming mat is compressed to a predetermined thickness by a hot press. Since a time of 10 seconds is required, the adhesive applied to the surface layer chip causes pre-curing on the mat surface which is always in contact with the hot platen, thereby deteriorating the fluidity of the adhesive in that portion. There was a disadvantage that the adhesive strength of the wood chip near the surface was weakened.

【0004】また、MDFの場合木材ファイバ−に上記
接着剤を塗布した後、高温のフラッシュドライヤ−に木
材ファイバ−を通して乾燥させていたので、加熱乾燥に
よる接着剤のプレキュアが生じて接着剤の流動性を悪化
させボ−ド全体の接着力が低下していた。
In the case of MDF, since the wood fiber is coated with the adhesive and then dried by passing the wood fiber through a high-temperature flash dryer, the adhesive is pre-cured by heating and drying, and the adhesive flows. And the adhesive strength of the entire board was reduced.

【0005】上記欠点を解消するために接着剤中にアン
モニア、ヘキサミン、苛性ソ−ダ等のアルカリ性物質ま
たはアルカリ性レゾ−ル型フェノ−ル樹脂(略してレゾ
−ル樹脂)を添加してPH値を高め、接着剤の硬化を遅
らせてプレキュアを抑制させる試みは既に行われてい
た。
In order to solve the above-mentioned drawbacks, an alkaline substance such as ammonia, hexamine, caustic soda or an alkaline resole type phenol resin (abbreviated as resole resin) is added to the adhesive to adjust the pH value. Attempts have been made to increase the stiffness and slow the curing of the adhesive to suppress precure.

【0006】しかしながら、アンモニア水やヘキサミ
ン、苛性ソ−ダ等は、製造工程中の加熱によって本来の
作用をなさずPH値が下がる傾向にあり、硬化遅延能力
は十分でなかった。また、レゾ−ル樹脂のみの添加では
硬化遅延能力は優れているものの、熱圧中の硬化速度が
必要以上に遅く熱圧時間が長くなり、製造コストや製造
効率の面で問題があった。
[0006] However, ammonia water, hexamine, caustic soda, etc., tend to lower their PH value due to heating during the production process without effecting their original function, and their curing retarding ability was not sufficient. In addition, although the addition of only a resin alone has an excellent curing delay ability, the curing speed during the application of heat and pressure is slower than necessary and the heat and pressure time is prolonged, which is problematic in terms of production cost and production efficiency.

【0007】[0007]

【上記欠点を解消するための手段】請求項1の発明は、
PB、MDF、OSBなど木質ボ−ドを製造する方法で
あり、木材チップや木材ストランド等の木削片や木材フ
ァイバ−に水性のアミノ系樹脂接着剤を塗布・撹拌しマ
ットを形成し所定厚さに熱圧成形し木質ボ−ドを製造す
るにあたり、上記アミノ接着剤に硬化遅延能力の優れた
アルカリ性レゾ−ル型フェノ−ル樹脂(略してレゾ−ル
樹脂)と硬化促進能力のある塩化アンモニウム等の硬化
促進剤、さらに親水性かつ親油性の有する溶媒を添加す
ることを特徴とする木質ボ−ドの製造方法を提供する。
[Means for solving the above disadvantages]
This is a method for manufacturing woody boards such as PB, MDF, OSB, etc., by applying and stirring an aqueous amino resin adhesive to wood chips and wood fibers such as wood chips and wood strands and wood fibers to form a mat having a predetermined thickness. In order to produce a wood board by hot-press molding, the amino adhesive has an alkaline resole type phenol resin (abbreviated as resole resin) having an excellent curing retarding ability and a chloride having a curing accelerating ability. Disclosed is a method for producing a wooden board, which comprises adding a curing accelerator such as ammonium and a solvent having hydrophilicity and lipophilicity.

【0008】上記レゾ−ル樹脂と硬化促進剤を配合した
場合、PH低下のためレゾ−ル樹脂が水不溶性となって
析出し、ポットライフが短くなるという問題があるの
で、親水性かつ親油性の有する溶媒すなわち、メチルア
ルコ−ルやエチルアルコ−ル等の水溶性アルコ−ルまた
はアセトン、ジメチルホルムアミド(DMF)、ジメチ
ルスルフォオキシド(DMSO)などをさらに添加し、
レゾ−ル樹脂の溶解性を上げることにより上記析出の問
題を解決する。
When the above-mentioned resole resin and a curing accelerator are blended, there is a problem that the resole resin becomes water-insoluble and precipitates due to a decrease in pH, and the pot life is shortened. , A water-soluble alcohol such as methyl alcohol or ethyl alcohol or acetone, dimethylformamide (DMF), dimethylsulfoxide (DMSO) or the like is further added.
The problem of the above precipitation is solved by increasing the solubility of the resin.

【0009】また、上記硬化促進剤として他に、硝酸ア
ンモニウムや硫酸アンモニウムなどの強酸と弱アルカリ
の塩、酢酸メチルや酢酸エチル、ギ酸エチルなどのエス
テルが挙げられる。さらにアミノ系接着剤として尿素樹
脂、尿素メラミン樹脂、メラミン樹脂、またはメラミン
フェノ−ル樹脂などが適している。なお、上記接着剤の
配合時のPH値は、8〜13のアルカリ性範囲であるこ
とが望ましい。
Other examples of the curing accelerator include salts of strong acids and weak alkalis such as ammonium nitrate and ammonium sulfate, and esters such as methyl acetate, ethyl acetate and ethyl formate. Further, urea resin, urea melamine resin, melamine resin, melamine phenol resin and the like are suitable as the amino adhesive. The PH value at the time of blending the adhesive is desirably in the alkaline range of 8 to 13.

【0010】さらに、請求項2の発明は、アミノ系接着
剤に添加するものとして請求項1の発明における添加剤
のほかPH調整剤、すなわちアンモニア、ヘキサミンま
たは苛性ソ−ダなどアルカリ性化合物を添加することを
特徴とする木質ボ−ドの製造方法を提供する。接着剤配
合時のPH値は、8〜13の範囲が望ましい。
Further, in the invention of claim 2, a pH adjuster, that is, an alkaline compound such as ammonia, hexamine or caustic soda is added to the amino-based adhesive in addition to the additive of the invention of claim 1. A method for producing a wooden board is provided. The PH value at the time of mixing the adhesive is preferably in the range of 8 to 13.

【0011】このように接着剤のPH値を上げることに
よりポットライフが長くプレキュアを防ぎ、かつ熱圧時
間を延長せずに木質ボ−ドの物性すなわち強度や耐水性
に優れた木質ボ−ドの製造方法を提供する。
[0011] By increasing the PH value of the adhesive in this manner, the pot life is long, precure is prevented, and the wood board having excellent physical properties, ie, strength and water resistance, without prolonging the hot pressing time. And a method for producing the same.

【0012】[0012]

【作用】請求項1の発明ではレゾ−ル樹脂の溶解性を高
め、木質ボ−ド製造工程中の接着剤のプレキュアを抑制
する。
According to the first aspect of the present invention, the solubility of the resin is enhanced, and the precuring of the adhesive during the wood board manufacturing process is suppressed.

【0013】請求項2の発明ではPH調整剤をさらに添
加することにより、いっそうレゾ−ル樹脂の溶解性を高
め、上記プレキュアをいっそう抑制する。
According to the second aspect of the present invention, by further adding a pH adjuster, the solubility of the resin is further enhanced, and the precure is further suppressed.

【0014】[0014]

【発明の実施の形態】接着剤の配合方法として樹脂分5
0%の水性アミノ系接着剤、例えばメラミン樹脂接着
剤、および親水性かつ親油性を有する溶媒、例えばメタ
ノ−ル、およびレゾ−ル樹脂、および硬化促進剤として
塩化アンモニウム水溶液を各々添加撹拌し接着剤を調整
する。
BEST MODE FOR CARRYING OUT THE INVENTION A resin content of 5
0% aqueous amino adhesive, for example, melamine resin adhesive, hydrophilic and lipophilic solvent, for example, methanol and resole resin, and ammonium chloride aqueous solution as a curing accelerator are added, stirred, and adhered. Adjust the agent.

【0015】高含水率の湿潤ファイバ−に上記調整した
接着剤を塗布し、フラッシュドライヤ−を通し、ファイ
バ−の含水率を20%以下にして乾燥させマット状にフ
ォ−ミングする。次いで200℃、26kgf/c
2、数分の熱圧条件でホットプレスを行い、所定厚
さ、所定比重の木質ボ−ド(MDF)を製造する。
The above-prepared adhesive is applied to the wet fiber having a high water content, passed through a flash dryer, dried with the fiber having a water content of 20% or less, and formed into a mat form. Then, at 200 ° C, 26 kgf / c
Hot pressing is performed under a heat pressure of m 2 for several minutes to produce a wood board (MDF) having a predetermined thickness and a specific gravity.

【0016】このようにして得られたMDFは、塩化ア
ンモニウムのみを配合に用いた接着剤を使って得られた
MDFよりも曲げ強度における残存率およびはく離強度
ともに高く、MDF内層の硬化が進んでいることがわか
る。
The MDF obtained in this manner has a higher residual ratio in flexural strength and a higher peeling strength than the MDF obtained by using an adhesive containing only ammonium chloride, and the hardening of the MDF inner layer proceeds. You can see that there is.

【0017】[0017]

【実施例】さらに本発明の実施例を4つ詳しく説明す
る。実施例1〜2および比較例1はMDF、実施例3〜
4および比較例2はPBを用いた場合の例である。
EXAMPLES Four examples of the present invention will be further described in detail. Examples 1 and 2 and Comparative Example 1 are MDF, Examples 3 to
4 and Comparative Example 2 are examples using PB.

【0018】(実施例1)配合方法として樹脂分50%
のメラミン樹脂接着剤200重量部にメタノ−ル3重量
部、樹脂分40%レゾ−ル樹脂2.5重量部、20%塩
化アンモニウム水溶液2.5重量部添加し撹拌して調整
した。湿潤ファイバ−に上記調整した接着剤を樹脂固形
分で15%塗布し、フラッシュドライヤ−を通し、含水
率20%以下に乾燥させる。次いでファイバ−をマット
状にフォ−ミングして200℃、26kgf/cm2
熱圧条件で3分間プレスを行った。この時の設定厚さ7
mm、設定比重0.75とした。このようにして得られ
たMDFは、塩化アンモニウムのみを配合に用いた場合
や塩化アンモニウムとヘキサミン(アルカリ物質)を添
加した場合に比して常態強度こそ僅少差であるが、残存
率やはく離強度ともに高くMDF内層の硬化が進んでい
た。
(Example 1) As a compounding method, a resin content of 50% was used.
3 parts by weight of methanol, 2.5 parts by weight of a 40% resin resin component, and 2.5 parts by weight of a 20% ammonium chloride aqueous solution were added to 200 parts by weight of the melamine resin adhesive of Example 1 to adjust the mixture by stirring. The above-prepared adhesive is applied to the wet fiber at a resin solid content of 15%, passed through a flash dryer, and dried to a water content of 20% or less. Next, the fiber was formed into a mat shape and pressed at 200 ° C. for 3 minutes under a heat and pressure condition of 26 kgf / cm 2 . Set thickness 7 at this time
mm and the set specific gravity 0.75. The MDF thus obtained has a slight difference in normal strength as compared with the case where only ammonium chloride is used in the compounding or the case where ammonium chloride and hexamine (alkali substance) are added, but the residual ratio and peeling strength are small. In both cases, the MDF inner layer was hardened.

【0019】(実施例2)配合方法として樹脂分50%
のメラミン樹脂接着剤200重量部にメタノ−ル6重量
部、樹脂分40%のレゾ−ル樹脂5重量部、20%塩化
アンモニウム水溶液5重量部添加し、さらに20%アン
モニア水1重量部加え撹拌して調整した。湿潤ファイバ
−に上記調整した接着剤を樹脂固形分で15%塗布し、
フラッシュドライヤ−を通し、含水率20%以下に乾燥
させた。次いでファイバ−をマット状にフォ−ミングし
て200℃、26kgf/cm2の熱圧条件で3分間プ
レスを行った。この時の設定厚さ7mm、設定比重0.
75とした。このようにして得られたMDFは実施例1
よりもさらに内層の硬化が進んでおり、湿潤時曲げ強度
やはく離強度、耐水性ともに向上した。
Example 2 As a compounding method, a resin content of 50% was used.
6 parts by weight of methanol, 5 parts by weight of a resin resin having a resin content of 40%, and 5 parts by weight of a 20% aqueous ammonium chloride solution were added to 200 parts by weight of a melamine resin adhesive, and further 1 part by weight of 20% aqueous ammonia was added and stirred. And adjusted. Applying the above-prepared adhesive to the wet fiber at a resin solid content of 15%,
It was dried through a flash dryer to a water content of 20% or less. Next, the fiber was formed into a mat shape and pressed at 200 ° C. for 3 minutes under a heat and pressure condition of 26 kgf / cm 2 . At this time, the set thickness is 7 mm, and the set specific gravity is 0.
75. The MDF obtained in this manner was obtained in Example 1.
The hardening of the inner layer has progressed further, and the bending strength when wet, the peeling strength, and the water resistance have all been improved.

【0020】(比較例1)配合方法として樹脂分50%
のメラミン樹脂接着剤に樹脂固形分に対して塩化アンモ
ニウム1%、ヘキサミン1%を添加して接着剤を調整し
た。湿潤ファイバ−に上記調整した接着剤を塗布した後
は、実施例1と同じである。なお、設定厚さ7mm、設
定比重0.75とした。
Comparative Example 1 Resin content 50%
1% of ammonium chloride and 1% of hexamine with respect to the resin solid content were added to the melamine resin adhesive of No. 1 to prepare the adhesive. After applying the above-prepared adhesive to the wet fiber, the procedure is the same as in Example 1. The set thickness was 7 mm and the set specific gravity was 0.75.

【0021】(実施例3)樹脂分50%の尿素樹脂接着
剤200重量部に、樹脂分40%レゾ−ル樹脂5重量
部、エタノ−ル10重量部、粉末塩化アンモニウム1重
量部を添加し撹拌し表層用接着剤を調整した。この接着
剤を絶乾木材チップ100重量部に対し樹脂固形分で1
2重量部塗布して表層用チップとした。また、樹脂分5
0%の尿素接着剤200重量部に塩化アンモニウム2重
量部添加し撹拌し内層用接着剤を調整した。この接着剤
を絶乾木材チップ100重量部に対し樹脂固形分で7重
量部塗布して内層用チップとした。このように表層用チ
ップと内層用チップを交互に積層して3層マットを構成
しホットプレスに挿入し、170℃、25kgf/cm
2の熱圧条件で3分間プレスし、厚さ12mm、設定比
重0.73のPBを成形した。得られたPBはサンダ−
がけしても、従来見られたプレキュア層による表面ザラ
ザラの凹凸感がほとんどなく平滑性が保持された。曲げ
強度も225kgf/cm2と従来のPBの曲げ強度よ
り高かった。
Example 3 To 200 parts by weight of a urea resin adhesive having a resin content of 50%, 5 parts by weight of a resin containing 40% resin, 10 parts by weight of ethanol, and 1 part by weight of powdered ammonium chloride were added. The mixture was stirred to prepare a surface layer adhesive. This adhesive is applied in a resin solid content of 1 to 100 parts by weight of a dry wood chip.
Two parts by weight were applied to obtain a surface layer chip. In addition, resin content 5
2 parts by weight of ammonium chloride was added to 200 parts by weight of a 0% urea adhesive and stirred to prepare an inner layer adhesive. This adhesive was applied at a resin solid content of 7 parts by weight to 100 parts by weight of a dry wood chip to obtain an inner layer chip. In this way, the surface layer chips and the inner layer chips are alternately laminated to form a three-layer mat, which is inserted into a hot press at 170 ° C. and 25 kgf / cm.
Pressing was performed for 3 minutes under the hot pressure conditions of 2 to form PB having a thickness of 12 mm and a specific gravity of 0.73. The obtained PB is sander
Even when the surface was peeled off, there was almost no unevenness of the surface due to the precured layer, which was conventionally seen, and the smoothness was maintained. The bending strength was 225 kgf / cm 2 , which was higher than that of the conventional PB.

【0022】(実施例4)樹脂分50%の尿素樹脂接着
剤200重量部に樹脂分40%のレゾ−ル樹脂8重量
部、メタノ−ル15重量部、粉末塩化アンモニウム2重
量部添加し、さらに25%のヘキサミン水を1重量部添
加し表層用接着剤を調整した。この接着剤を絶乾木材チ
ップ100重量部に対し、樹脂固形分で15重量部塗布
して表層用チップとした。また、樹脂分50%の尿素メ
ラミン樹脂接着剤200重量部に塩化アンモニウム2重
量部添加し撹拌し内層用接着剤を調整した。この接着剤
を絶乾木材チップ100重量部に対し樹脂固形分で10
重量部塗布して内層用チップとした。このようにして得
られた表層用チップと内層用チップを交互に積層して3
層マットを構成しホットプレスに挿入し、170℃、2
5kgf/cm2の熱圧条件で3.5分間プレスし、厚
さ15mm、設定比重0.73のPBを成形した。得ら
れたPBはサンダ−がけしても、実施例3と同じように
表面の平滑性は保持された。曲げ強度も230kgf/
cm2と従来のPBの曲げ強度より高かった。
Example 4 To 200 parts by weight of a urea resin adhesive having a resin content of 50%, 8 parts by weight of a resin containing 40% of resin, 15 parts by weight of methanol, and 2 parts by weight of powdered ammonium chloride were added. Further, 1 part by weight of 25% aqueous hexamine was added to prepare a surface layer adhesive. This adhesive was applied to 100 parts by weight of absolutely dry wood chips at a resin solid content of 15 parts by weight to obtain a surface layer chip. Also, 2 parts by weight of ammonium chloride was added to 200 parts by weight of a urea melamine resin adhesive having a resin content of 50%, and the mixture was stirred to prepare an inner layer adhesive. This adhesive is applied in a resin solid content of 10 parts by weight to 100 parts by weight of a dry wood chip.
Parts by weight were applied to obtain inner layer chips. The chip for the surface layer and the chip for the inner layer obtained in this manner are alternately laminated to obtain 3
Construct layer mat and insert into hot press, 170 ° C, 2
Pressing was performed for 3.5 minutes under a heat and pressure condition of 5 kgf / cm 2 to form PB having a thickness of 15 mm and a specific gravity of 0.73. Even when the obtained PB was sanded, the surface smoothness was maintained as in Example 3. The bending strength is 230kgf /
cm 2 , higher than the bending strength of conventional PB.

【0023】(比較例2)配合方法として樹脂分50%
の尿素樹脂接着剤に樹脂固形分に対して表層用の場合、
塩化アンモニウム1%、ヘキサミン1%を添加し、内層
用の場合、塩化アンモニウム1%添加し、接着剤を調整
した。その他の製造工程は実施例4と同じようにした。
このようにして得られたPBは厚さ15mm、設定比重
0.73とした。
(Comparative Example 2) As a compounding method, a resin content of 50%
In the case of urea resin adhesive for surface layer with respect to resin solid content,
1% of ammonium chloride and 1% of hexamine were added, and for the inner layer, 1% of ammonium chloride was added to adjust the adhesive. Other manufacturing steps were the same as in Example 4.
The PB thus obtained had a thickness of 15 mm and a specific gravity of 0.73.

【0024】以上4つの実施例および2つの比較例で製
造されたMDF、PBの試験片についてJIS規格に示
されている曲げ強度試験、湿潤時曲げ強度B試験、およ
びはく離強度試験を行った。その試験結果を表1および
表2に示す。
The MDF and PB test pieces manufactured in the above four examples and two comparative examples were subjected to a bending strength test, a wet bending strength B test, and a peel strength test specified in JIS standards. The test results are shown in Tables 1 and 2.

【0025】[0025]

【表1】 [Table 1]

【0026】[0026]

【表2】 [Table 2]

【0027】なお、上記試験方法として曲げ強度試験で
は、所定厚さ(mm)、幅50mm、長さ200mm、
スパン長150mmの試験片を準備し、この試験片表面
中央から荷重を加えその最大荷重を測定した。湿潤時曲
げ強度B試験では、所定厚さ(mm)、幅50mm、長
さ200mm、スパン長150mmの試験片を沸騰水中
に2時間浸漬、さらに常温水中に1時間浸漬した後、濡
れたままの状態で上記した試験方法で同じように行っ
た。はく離強度試験では、所定厚さ(mm)、幅50m
m、長さ50mmの試験片をはく離試験治具に取り付
け、試験片の内部はく離試験を行って内部はく離力を求
め、その値を試験片面積25cm2で割って1cm2当た
りの内部はく離応力(kgf/cm2)を求めた。上記
曲げ強度(kgf/cm2)は3PL/2bt2 であり、
ここでPは最大荷重、Lはスパン長、bは試験片の幅、
tは同厚さである。また表の中、残存率(%)は湿潤時
曲げ強度B(kgf/cm2)を曲げ強度(kgf/c
2)で割って100を乗じた値であり、耐水性の度合
いを示す。
The above-mentioned test method is a bending strength test.
Is a predetermined thickness (mm), width 50 mm, length 200 mm,
A test piece with a span length of 150 mm was prepared, and the surface of the test piece was prepared.
A load was applied from the center and the maximum load was measured. Song when wet
In the strength B test, the specified thickness (mm), width 50 mm, length
200mm long, 150mm span test piece in boiling water
After immersion for 2 hours in water at room temperature for 1 hour,
Perform the same procedure with the test method
Was. In the peel strength test, predetermined thickness (mm), width 50m
Attach a 50 mm long test piece to a peeling jig
Internal peel test of the test piece to determine the internal peel force.
And the value is 25 cmTwoDivided by 1cmTwoHit
Internal peeling stress (kgf / cmTwo). the above
Flexural strength (kgf / cmTwo) Is 3PL / 2btTwo And
Where P is the maximum load, L is the span length, b is the width of the test piece,
t is the same thickness. Also, in the table, the residual rate (%)
Bending strength B (kgf / cmTwo) Is the bending strength (kgf / c)
mTwo) And multiplied by 100 to determine the degree of water resistance.
Indicates that

【0028】(考察)上記表1から明らかなように、各
々実施例の試験片は比較例の試験片に比べて常態曲げ強
度および湿潤時曲げ強度Bは高くなっている。さらに、
表2から明らかなように、曲げ強度やはく離強度が比較
例に比べて高いことから、表層のプレキュアが抑制さ
れ、内層まで硬化が進んでいることがわかる。
(Consideration) As is apparent from Table 1 above, the test piece of each example has a higher normal bending strength and wet bending strength B than the test piece of the comparative example. further,
As is clear from Table 2, since the bending strength and the peeling strength are higher than those of the comparative examples, it can be seen that the precure of the surface layer is suppressed and the curing is progressing to the inner layer.

【0029】また、表1から明らかなように、耐水性や
はく離強度においても比較例のそれに比べて高い値を示
しており、この結果からボ−ドの内層まで硬化が進んで
おり、フラッシュドライヤ−通過時でのプレキュアによ
る接着不良等が抑制されたものと思われる。
Further, as is clear from Table 1, the water resistance and the peel strength are higher than those of the comparative example, and from this result, the curing is progressing to the inner layer of the board, and the flash dryer is used. -It is considered that poor adhesion due to pre-curing at the time of passage was suppressed.

【0030】[0030]

【発明の効果】請求項1の発明によれば木質ボ−ドの製
造工程中、接着剤のプレキュアを抑制することで、木質
ボ−ド中の木削片間やファイバ−間を結合する接着剤の
接着力が従来より高まり、木質ボ−ドの曲げ強度やはく
離強度、耐水性の向上が見られた。
According to the first aspect of the present invention, by suppressing the pre-curing of the adhesive during the manufacturing process of the wood board, the bonding between the wood chips and the fibers in the wood board is achieved. The adhesive strength of the agent was higher than before, and the bending strength, peeling strength and water resistance of the wooden board were improved.

【0031】請求項2の発明によれば、さらに上記接着
剤にPH調整剤を添加することによって、請求項1の発
明よりもレゾ−ル樹脂の溶解度を高め、その結果PH値
を高め、ポットライフがボ−ド製造に支障を起こさない
ように保持される。したがって、プレキュアがいっそう
抑制され、木質ボ−ドの強度、耐水性も向上した。
According to the second aspect of the present invention, by further adding a pH adjuster to the adhesive, the solubility of the resole resin is increased as compared with the first aspect of the present invention, and as a result, the PH value is increased. Life is maintained so as not to interfere with board manufacture. Therefore, the precure was further suppressed, and the strength and water resistance of the wooden board were also improved.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 木材チップや木材ストランド等の木削片
または木材ファイバ−にアミノ系接着剤を塗布しフォ−
ミングマットを形成して後、所定厚みに熱圧成形して木
質ボ−ドを製造する方法において、上記接着剤にレゾ−
ル型フェノ−ル樹脂、硬化促進剤および親水性かつ親油
性を有する溶媒を添加することを特徴とする木質ボ−ド
の製造方法。
1. An amino-based adhesive is applied to wood chips or wood fibers such as wood chips and wood strands to form
In a method of manufacturing a wooden board by forming a mining mat and then hot pressing to a predetermined thickness, a resin is applied to the adhesive.
A method for producing a wood board, comprising adding a phenolic resin, a curing accelerator and a hydrophilic and lipophilic solvent.
【請求項2】 前記アミノ系接着剤にレゾ−ル型フェノ
−ル樹脂、硬化促進剤および親水性かつ親油性を有する
溶媒のほか、さらにPH調整剤を添加することを特徴と
する請求項1記載の木質ボ−ドの製造方法。
2. The amino-based adhesive further comprises a pH adjuster in addition to a resol-type phenolic resin, a curing accelerator and a hydrophilic and lipophilic solvent. A method for producing the woody board described.
JP32768196A 1996-11-22 1996-11-22 Manufacture of woody board Withdrawn JPH10151608A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP32768196A JPH10151608A (en) 1996-11-22 1996-11-22 Manufacture of woody board

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP32768196A JPH10151608A (en) 1996-11-22 1996-11-22 Manufacture of woody board

Publications (1)

Publication Number Publication Date
JPH10151608A true JPH10151608A (en) 1998-06-09

Family

ID=18201796

Family Applications (1)

Application Number Title Priority Date Filing Date
JP32768196A Withdrawn JPH10151608A (en) 1996-11-22 1996-11-22 Manufacture of woody board

Country Status (1)

Country Link
JP (1) JPH10151608A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014031019A (en) * 2013-10-04 2014-02-20 Noda Corp Woody fiber board

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014031019A (en) * 2013-10-04 2014-02-20 Noda Corp Woody fiber board

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