JPH043721B2 - - Google Patents

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Publication number
JPH043721B2
JPH043721B2 JP59097566A JP9756684A JPH043721B2 JP H043721 B2 JPH043721 B2 JP H043721B2 JP 59097566 A JP59097566 A JP 59097566A JP 9756684 A JP9756684 A JP 9756684A JP H043721 B2 JPH043721 B2 JP H043721B2
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JP
Japan
Prior art keywords
plywood
veneer
adhesive
moisture content
layer
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.)
Expired - Lifetime
Application number
JP59097566A
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Japanese (ja)
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JPS60242001A (en
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Filing date
Publication date
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Priority to JP9756684A priority Critical patent/JPS60242001A/en
Publication of JPS60242001A publication Critical patent/JPS60242001A/en
Publication of JPH043721B2 publication Critical patent/JPH043721B2/ja
Granted legal-status Critical Current

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  • Veneer Processing And Manufacture Of Plywood (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は合板の製造法に関するものである。 〔従来技術〕 通常、合板は表裏第1層の単板はその繊維方向
を合板の長手方向に平行に、第2層は第1層に直
交するように、第3層は第2層に直交するように
(すなわち第1層には平行に)、第4層は第3層に
直交(第2層に平行に)するように、隣接する単
板同士直交するように構成されている。第1層,
第3層,第5層……など奇数層の単板は繊維方向
の長さが長いので良質の長尺原木を使用するが、
高価なためなるべく薄く剥板し使用する。逆に偶
数層の単板は低質材を厚く剥板し、合板の厚みの
うちなるべく偶数層単板が多く占めるように配慮
される。従つて、ドライヤで単板を乾燥させる場
合、奇数層の単板は薄いため乾燥は容易である
が、偶数層単板は厚いため当然ドライヤの運転ス
ピードを大幅に低下させる必要があり、工場全体
の生産性に悪影響を及ぼしている。工場設備中最
も高価なドライヤの大型化は大きい出費と必然的
にボイラーの能力アツプ、煙突の大型化、排煙脱
硫防塵等公害防止設備の大型化などが必要になり
容易なことではない。また原価的にみると、合板
原価に占める原木のウエイトは原木の価格、石油
の価格などに左右されるので一定ではないが、近
年70%前後を占めるため原木から合板への歩留り
をいかに向上させるかが最大のポイントになつて
いる。このための手段として高性能ロータリー
レースの導入による原木の単板化率の向上(剥芯
が細くなるまで剥板する)、小巾単板の集約的
使用、単板の乾燥度を減少させることにより熱
エネルギコストの削減、ドライヤ稼動率の向上を
図り、乾燥収縮を減少させ、乾燥によるワレ、カ
ケ、オドリを減少し、合わせて大幅に単板から合
板への転化率を向上させる、などが考えられる。 このように、高含水率単板を有効に利用できれ
ば極めて大きなメリツトが生まれるが、現状では
単板含水率を高くした時に生じる汚染、パンク、
表面ワレの問題が解決されていないため、普通含
水率18%以下、好ましくは12%以下で使用されて
いる。例えば合板を構成する単板を含水率20%以
上でユリア系、メラミン系、ユリア・メラミン
系、ユリア・フエノール系、メラミン・ユリア・
フエノール系、メラミン・フエノール系などアミ
ノ系樹脂接着剤を用いて合板を生産すると、接
着剤層の水分が単板の方に移行しないため、接着
剤の濃縮化がなされず硬化反応が著しく遅延し、
プレス開締時単板間の接着力が不充分で接着力が
水蒸気の圧力以下の部分がすべてパンクし、また
接着剤が接着剤中の高温水により洗い流され広範
囲の欠膠部分を発生し、各層単板がバラバラにな
るなど満足な接着が得られない。表、裏のそれ
ぞれ第1層単板が多くの水分を含んだ状態でホツ
トプレスのスチール製熱板に直接接触するため、
タンニン−鉄反応により合板表面が全面的に黒変
し、合板としての商品価値を著しく低下してしま
う。ホツトプレスから取り出した時、表裏のそ
れぞれ第1層単板の表面に熱収縮や脱水収縮によ
る無数のワレを生じ、塗装、プリント紙貼り、ツ
キ板貼りなどの2次加工性を不可能にするほど表
面品質を低下させる。ウレタン系、エポキシ系
など湿気硬化や湿潤接着可能な接着剤を使用すれ
ば前記の問題はないが著しく高価(接着剤価格
で4〜5倍以上)であり、また前記,の問題
はまぬがれないし、ホツトプレス時の硬化はアミ
ノ系樹脂接着剤に較べて著しく遅い。ウレタン
系、エポキシ系の接着剤を使用し、常温接着すれ
ば前記の問題はないが、硬化に著しく長時間を
要し、生産性が致命的に悪化してしまう。例えば
3mm3プライ合板を製造する場合アミノ系接着剤
では、110℃、60秒のホツトプレスでよいが、ウ
レタン系、エポキシ系接着剤による常温プレスで
は3〜12時間必要である。 〔発明の目的〕 本発明者等はアミノ系樹脂接着剤にイソシアネ
ート化合物を多量に併用すること、及び表裏の第
1層に乾燥単板を用いることにより前記各問題点
をすべて解消出来ることを見出し、本発明を完成
させるに至つた。 〔発明の構成〕 本発明は、アミノ系樹脂接着剤を用いて合板を
生産する方法に於いて、表及び裏のそれぞれ第
1層の単板として含水率18%以下のものを使用す
ること、表及び裏から偶数番目の単板として含
水率20%以上のものを使用すること、水性アミ
ノ系樹脂接着剤100部に対し、イソシアネート化
合物8部以上を含有する配合物を接着剤として使
用することを特徴とする合板の製造方法である。 次に本発明を更に詳しく説明する。 単板はドライヤで乾燥するにつれ含水率が低下
して行くが、繊維飽和点までは収縮せず、これ以
下になつて収縮がはじまる。収縮に伴い歩留が低
下するだけでなく単板はどんどんもろくなり、ワ
レ、カケが急に増大傾向を示し始め、単板周辺部
のオドリも増大して来る。従つて、含水率が少し
でも多い単板で合板を生産することが歩留向上や
コストダウンに大きく貢献するが、前述の如く多
くの問題を惹起する。従つて、現状では止むを得
ず、全体的に平均して単板含水率18%以下で使用
されている。本発明の方法は表裏第1層単板は含
水率18%以下にするが単板厚味の厚い偶数層単板
は20%以上の高含水率で使用することを可能に
し、大いに歩留り効果を期待出来るものとした。
更に言えば、表裏第1層以外の奇数層単板は含水
率18%以下としてもよいが、好ましい条件さえ見
出せば表裏第1層以外のすべての単板を20%以上
で使用することも出来る極めて有用な方法を提供
するものである。 本発明において、水性アミノ系樹脂接続剤と
は、ユリア、メラミン、ユリア・メラミン、ユリ
ア・フエノール、メラミン・ユリア・フエノー
ル、メラミン・フエノールなどアミノ系化合物を
含む、ホルムアルデヒドと反応性のある化合物と
ホルムアルデヒドとの反応によつて得られた縮合
物からなる水性接着剤である。 本発明で言うイソシアネート化合物とはTDI,
MDI、クルードMDIなど分子中にイソシアネー
ト基を2基以上もつ化合物をいう。TDI,MDI,
クルードMDIなどのように分子量に対しイソシ
アネート基の割合の多いものは比較的少量の添加
で効果があるが、各種プレポリマー、例えばGA
−704(住友ベークライト製、エチレンオキサイ
ド、プロピレンオキサイド系ポリエーテルと
MDIとの反応により得られた両末端イソシアネ
ート基のプレポリマー)では比較的多く添加する
ことが好ましい。コスト、入手の容易さ、保存安
定性などの面からクルードMDIが最も好ましい。
イソシアネート化合物の添加量は水性接着剤の架
橋用には1〜5%が一般的であるが、本発明の場
合は8%以上好ましくは15〜30%がよく8%以下
では顕著な効果はない。 〔発明の効果〕 本発明は表裏第1層単板の含水率を18%以下
として表面汚染を回避し、安価な水性アミノ系
樹脂接着剤に8%以上のイソシアネート化合物を
添加した配合物を使用することにより、高含水率
単板の仮接着と接着を可能にし、偶数層単板を
20%以上の高含水率にすることにより合板の歩留
り、生産性、経済性を大巾に向上し得た工業上有
用な合板の生産方法である。 なお、ユリア系、メラミン系接着剤使用の場
合、クルイン、カチヤ、アピトン、ニアトー、ラ
ミン、ケンパス、エリマ、シナ、ニレ材等は難接
着材とされ、充分な接着力を示さないことが多い
が、本発明のイソシアネート化合物を配合したア
ミノ系接着剤を使用すればラワン同様の良好な接
着力を示すことがわかつた。 〔実施例〕 次に実施例について説明する。 実施例 1 厚み1.4mmと4.0mmのラワン単板につき第1表の
合板No.に従い含水率をそれぞれ調整し、合板素材
を準備した。次にユリア系接着剤ヰゲタライム
UA−126(住友ベークライト製一般市販品種:50
%樹脂水溶液)及びメラミン系接着剤ヰゲタライ
ムMA−204(住友ベークライト製一般市販品種:
53%樹脂水溶液)を第2表のA,Cの通り配合
し、更にB,Dの通りUA,MAの15%相当量の
クルードMDIを配合した。第1表の各種含水率
の合板素材に第2表の配合接着剤を1グルーライ
ン当り200g/m2の割合で表第2層及び裏第2層
の単板(4.0mm単板)の表裏に塗布し、15分間冷
圧の後10Kg/cm2の圧力下、110℃、180秒間ホツト
プレスし、12mm合板を作成した。配合A,Bを使
用した合板はJASタイプ2規格テストにより、
C,Dを使用した合板はJASタイプ1規格により
接着力テストを実施し、第3表に示すように合格
(〇印)、再試験(△印)、不合格(×印)等の結
果を示した。AとB、CとDの比較によりイソシ
アネート化合物の添加が高含水率単板の接着を可
能にすることがわかる。但し、合板No.7,8は表
裏第1層単板の含水率が高いため、接着の可否に
かかわらず表裏単板は黒色に着色し、商品価値の
著しく劣るものになつた。また配合A,Cの場合
高含水率単板では冷圧中に仮接着状態に至らず、
ホツトプレスの自動挿入設備が使用出来なかつ
た。これは工場生産上大きな問題であることを示
している。B,Dは完壁の仮接着性を示し実用上
極めて良好であることがわかる。
[Industrial Application Field] The present invention relates to a method for manufacturing plywood. [Prior art] Normally, the fiber direction of the first layer of plywood is parallel to the longitudinal direction of the plywood, the second layer is orthogonal to the first layer, and the third layer is orthogonal to the second layer. The fourth layer is configured to be perpendicular to the third layer (parallel to the second layer), and the adjacent veneers are configured to be perpendicular to each other. 1st layer,
For odd-numbered layers such as the 3rd layer, 5th layer, etc., the length in the fiber direction is long, so high-quality long logs are used.
Since it is expensive, it is used by stripping it as thinly as possible. On the other hand, for even-numbered veneers, low-quality material is peeled thickly so that the even-numbered veneers account for as much of the plywood thickness as possible. Therefore, when drying veneers in a dryer, the odd-numbered veneers are thin and easy to dry, but the even-layered veneers are thick, so naturally the dryer operating speed must be significantly reduced, and the entire factory is having a negative impact on productivity. Enlarging the size of the dryer, which is the most expensive piece of factory equipment, is not an easy task as it requires a large expense and necessarily increases the capacity of the boiler, increases the size of the chimney, and increases the size of pollution prevention equipment such as flue gas desulfurization and dust control. In terms of cost, the weight of raw wood in the plywood cost is not constant as it depends on the price of raw wood, the price of oil, etc., but in recent years it has accounted for around 70%, so it is important to consider how to improve the yield from raw wood to plywood. That is the biggest point. As a means of achieving this, we have introduced high-performance rotary laces to improve the rate of veneerization of raw wood (stripping until the core becomes thin), intensive use of narrow veneers, and reduced dryness of veneers. This reduces thermal energy costs, improves dryer operation rate, reduces drying shrinkage, reduces cracks, chips, and looseness caused by drying, and significantly improves the conversion rate from veneer to plywood. Conceivable. In this way, if high moisture content veneer could be used effectively, it would bring extremely great benefits, but at present, the pollution, punctures, etc. that occur when the moisture content of veneer is increased are
Since the problem of surface cracking has not been solved, it is usually used at a moisture content of 18% or less, preferably 12% or less. For example, if the veneer that makes up plywood has a moisture content of 20% or more, urea type, melamine type, urea/melamine type, urea/phenol type, melamine/urea type, etc.
When plywood is produced using amino-based resin adhesives such as phenol-based, melamine/phenol-based, etc., moisture in the adhesive layer does not transfer to the veneer, so the adhesive does not become concentrated and the curing reaction is significantly delayed. ,
When the press was opened and closed, the adhesive force between the veneers was insufficient, causing punctures in all areas where the adhesive force was less than the pressure of water vapor, and the adhesive was washed away by the high temperature water in the adhesive, causing a wide range of non-stick areas. Satisfactory adhesion cannot be obtained as each layer of veneer falls apart. Because the first layer of veneer on the front and back sides contains a lot of moisture and comes into direct contact with the hot press steel heating plate,
The tannin-iron reaction causes the entire plywood surface to turn black, significantly reducing the commercial value of the plywood. When taken out from the hot press, numerous cracks appeared on the surface of the first layer veneer on both the front and back sides due to heat shrinkage and dehydration shrinkage, making secondary processing such as painting, printing paper pasting, veneer pasting impossible. Reduces surface quality. If moisture curing or wet bonding adhesives such as urethane or epoxy adhesives are used, the above problems will not occur, but they are extremely expensive (more than 4 to 5 times the adhesive price), and the above problems cannot be avoided. Curing during hot pressing is significantly slower than that of amino resin adhesives. If a urethane-based or epoxy-based adhesive is used and bonded at room temperature, the above-mentioned problem will not occur, but curing will take an extremely long time, resulting in a fatal decline in productivity. For example, when manufacturing 3 mm 3-ply plywood, hot pressing at 110° C. for 60 seconds is sufficient when using an amino adhesive, but room temperature pressing using a urethane or epoxy adhesive requires 3 to 12 hours. [Object of the Invention] The present inventors have discovered that all of the above problems can be solved by using a large amount of an isocyanate compound in an amino resin adhesive and by using a dry veneer for the first layer on the front and back sides. , we have completed the present invention. [Structure of the Invention] The present invention provides a method for producing plywood using an amino-based resin adhesive, in which a veneer with a moisture content of 18% or less is used as the first layer veneer on each of the front and back sides; Use a moisture content of 20% or more as the even-numbered veneer from the front and back, and use a compound containing 8 parts or more of an isocyanate compound per 100 parts of aqueous amino resin adhesive as an adhesive. This is a method for manufacturing plywood characterized by the following. Next, the present invention will be explained in more detail. As the veneer dries in a dryer, its moisture content decreases, but it does not shrink until it reaches the fiber saturation point, and begins to shrink below this point. Not only does the yield decrease with shrinkage, but the veneer becomes more and more brittle, cracks and chips suddenly begin to increase, and the number of dents around the veneer also increases. Therefore, producing plywood using veneers with even a slightly higher moisture content greatly contributes to improving yields and reducing costs, but it causes many problems as described above. Therefore, at present it is unavoidable that veneers are used at an average moisture content of 18% or less overall. The method of the present invention allows the first layer veneer on the front and back sides to have a moisture content of 18% or less, but thick even-numbered veneers can be used with a moisture content of 20% or more, which greatly improves yield. It was something to look forward to.
Furthermore, odd-numbered veneers other than the first layer on the front and back sides may have a moisture content of 18% or less, but if favorable conditions are found, all veneers other than the first layer on the front and back sides can be used with a moisture content of 20% or more. This provides an extremely useful method. In the present invention, the aqueous amino resin connecting agent refers to compounds reactive with formaldehyde, including amino compounds such as urea, melamine, urea melamine, urea phenol, melamine urea phenol, and melamine phenol. This is an aqueous adhesive consisting of a condensate obtained by a reaction with The isocyanate compounds referred to in the present invention are TDI,
Refers to compounds with two or more isocyanate groups in the molecule, such as MDI and crude MDI. TDI, MDI,
Products with a high proportion of isocyanate groups relative to their molecular weight, such as crude MDI, are effective when added in relatively small amounts, but various prepolymers, such as GA
−704 (manufactured by Sumitomo Bakelite, ethylene oxide, propylene oxide polyether and
In the case of a prepolymer (prepolymer having isocyanate groups at both ends obtained by reaction with MDI), it is preferable to add a relatively large amount. Crude MDI is most preferred in terms of cost, ease of availability, storage stability, etc.
The amount of isocyanate compound added is generally 1 to 5% for crosslinking water-based adhesives, but in the case of the present invention, it is 8% or more, preferably 15 to 30%, and if it is less than 8%, there is no noticeable effect. . [Effects of the Invention] The present invention avoids surface contamination by setting the moisture content of the front and back first layer veneers to 18% or less, and uses a formulation in which 8% or more of an isocyanate compound is added to an inexpensive water-based amino resin adhesive. This enables temporary adhesion and adhesion of high moisture content veneers, and even-layered veneers.
This is an industrially useful plywood production method that greatly improves the yield, productivity, and economic efficiency of plywood by increasing the moisture content to 20% or more. In addition, when using urea-based or melamine-based adhesives, materials such as Kluin, Katya, Apitone, Nyato, Ramin, Kempas, Elima, China, and Elm are considered to be difficult to adhere to and often do not exhibit sufficient adhesive strength. It has been found that the use of an amino adhesive containing the isocyanate compound of the present invention exhibits good adhesive strength similar to that of lauan. [Example] Next, an example will be described. Example 1 For 1.4 mm and 4.0 mm thick lauan veneers, the moisture content was adjusted according to the plywood numbers in Table 1, and plywood materials were prepared. Next is the urea adhesive Vigetalime.
UA-126 (manufactured by Sumitomo Bakelite, commercially available type: 50
% resin aqueous solution) and melamine adhesive Vigetalime MA-204 (commercially available product manufactured by Sumitomo Bakelite:
A 53% resin aqueous solution) was blended as shown in A and C in Table 2, and crude MDI equivalent to 15% of UA and MA was blended as shown in B and D. Apply the compounded adhesive shown in Table 2 to plywood materials with various moisture contents shown in Table 1 at a rate of 200 g/m 2 per glue line on the front and back sides of the veneer (4.0 mm veneer) for the front second layer and the back second layer. After cold pressing for 15 minutes, hot pressing was carried out at 110° C. for 180 seconds under a pressure of 10 kg/cm 2 to produce 12 mm plywood. Plywood using combinations A and B was tested according to the JAS Type 2 standard.
Plywood using C and D was subjected to an adhesion test according to the JAS Type 1 standard, and as shown in Table 3, the results were passed (○ mark), retested (△ mark), failed (x mark), etc. Indicated. A comparison of A and B and C and D shows that the addition of an isocyanate compound enables adhesion of high moisture content veneers. However, since the moisture content of the first layer of plywood No. 7 and 8 was high, the front and back veneers were colored black regardless of whether they were bonded or not, resulting in significantly inferior commercial value. In addition, in the case of formulations A and C, high moisture content veneers do not reach temporary adhesion during cold pressing,
The automatic insertion equipment of the hot press could not be used. This indicates a major problem in factory production. It can be seen that B and D exhibit perfect temporary adhesion and are extremely good in practical use.

【表】【table】

【表】【table】

【表】 ○:合格 △:再試験 ×:不合格
実施例 2 単板構成及び単板含水率を第1表の合板No.4と
同じとし単板種類を難接着材6種、、接着剤配合
を第2表のA,B,C,Dとして実施例1と同様
にして合板を作成し、実施例1と同じくJASタイ
プ2、タイプ1規格による接着力テストを行い第
4表に示す結果を得た。これよりユリア系、メラ
ミン系などアミノ系樹脂接着剤では難接着材に対
しても本発明のイソシアネート化合物配合接着剤
が有効なことを示した。
[Table] ○: Pass △: Retest ×: Fail Example 2 The veneer composition and moisture content are the same as plywood No. 4 in Table 1, and the veneer types are 6 types of difficult-to-adhesive materials, adhesives Plywood was made in the same manner as in Example 1 using the compositions A, B, C, and D in Table 2, and the adhesion test was conducted according to the JAS Type 2 and Type 1 standards as in Example 1, and the results are shown in Table 4. I got it. This indicates that the isocyanate compound-containing adhesive of the present invention is effective even for materials that are difficult to bond with amino-based resin adhesives such as urea-based and melamine-based adhesives.

【表】 ○:合格 ×:不合格
[Table] ○: Pass ×: Fail

Claims (1)

【特許請求の範囲】[Claims] 1 アミノ樹脂接着剤を用いて合板を生産する方
法に於いて、表及び裏のそれぞれ第1層の単板
として含水率18%以下のものを使用すること、
表及び裏から偶数番目の単板として含水率20%以
上のものを使用すること、水性アミノ系樹脂接
着剤100部に対し、イソシアネート化合物8部以
上を含有する配合物を接着剤として使用するこ
と、を特徴とする合板の製造方法。
1. In the method of producing plywood using amino resin adhesive, use a veneer with a moisture content of 18% or less as the first layer of veneer on each of the front and back sides,
Use a moisture content of 20% or more as the even-numbered veneer from the front and back, and use a compound containing 8 parts or more of an isocyanate compound per 100 parts of aqueous amino resin adhesive as an adhesive. A method for manufacturing plywood, characterized by:
JP9756684A 1984-05-17 1984-05-17 Manufacture of flitch Granted JPS60242001A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9756684A JPS60242001A (en) 1984-05-17 1984-05-17 Manufacture of flitch

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9756684A JPS60242001A (en) 1984-05-17 1984-05-17 Manufacture of flitch

Publications (2)

Publication Number Publication Date
JPS60242001A JPS60242001A (en) 1985-12-02
JPH043721B2 true JPH043721B2 (en) 1992-01-24

Family

ID=14195779

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9756684A Granted JPS60242001A (en) 1984-05-17 1984-05-17 Manufacture of flitch

Country Status (1)

Country Link
JP (1) JPS60242001A (en)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4930429A (en) * 1972-07-04 1974-03-18
JPS5893766A (en) * 1981-11-30 1983-06-03 Nippon Urethane Service:Kk Adhesive composition consisting of self-emulsifiable polyisocyanate and formalin condensation resin
JPS58185669A (en) * 1982-04-22 1983-10-29 Eidai Co Ltd Preparation of adhesive
JPS58191140A (en) * 1982-04-30 1983-11-08 Eidai Co Ltd Manufacturing method of particle board

Also Published As

Publication number Publication date
JPS60242001A (en) 1985-12-02

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