JPH08134424A - Binder for structural composite - Google Patents

Binder for structural composite

Info

Publication number
JPH08134424A
JPH08134424A JP27115294A JP27115294A JPH08134424A JP H08134424 A JPH08134424 A JP H08134424A JP 27115294 A JP27115294 A JP 27115294A JP 27115294 A JP27115294 A JP 27115294A JP H08134424 A JPH08134424 A JP H08134424A
Authority
JP
Japan
Prior art keywords
binder
structural composite
mol
phenol
resin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP27115294A
Other languages
Japanese (ja)
Inventor
Taisei Omura
大成 大村
Tadao Kobayashi
忠生 小林
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.)
SHIN NIPPON GIKEN KK
Original Assignee
SHIN NIPPON GIKEN KK
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 SHIN NIPPON GIKEN KK filed Critical SHIN NIPPON GIKEN KK
Priority to JP27115294A priority Critical patent/JPH08134424A/en
Publication of JPH08134424A publication Critical patent/JPH08134424A/en
Pending legal-status Critical Current

Links

Landscapes

  • Dry Formation Of Fiberboard And The Like (AREA)
  • Phenolic Resins Or Amino Resins (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

PURPOSE: To provide a binder for a structural composite which can improve the strengths of a structural composite. CONSTITUTION: The binder is obtd. by reacting 1mol of phenol with 1-2mol of formaldehyde in the presence of a catalyst comprising 0.05-0.2mol of caustic soda and 0.01-0.1mol of ammonia and has a number average mol.wt. of 300-600.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、構造用複合材の製造に
用いるバインダーに関するものである。ここで構造用複
合材とは、例えばパーティクルボードと称される複合材
のように、木粉や木質小片等のマトリックス材に接着剤
としての役目を果すバインダーを混ぜ合わせて加熱加圧
し板状や角棒状に成形された材料をいい、用途としては
床板や壁板,野地板などの建築構築用材料として用いら
れたり、運搬・保管用パレットを構成する材料(天板及
び桁材)として用いられる。
FIELD OF THE INVENTION The present invention relates to a binder used in the production of structural composite materials. Here, the structural composite material, for example, like a composite material called particle board, a matrix material such as wood powder or wood chips is mixed with a binder serving as an adhesive, heated and pressed to form a plate or It is a material shaped like a square rod, and is used as a building construction material such as floor boards, wall boards, and ground boards, and as a material that constitutes a pallet for transportation and storage (top board and girder material). .

【0002】[0002]

【従来の技術】この種構造用複合材の製造に用いるバイ
ンダーとしては、従来からアルカリレゾール型の液状フ
ェノール樹脂が多く使用されている。しかし乍ら、従来
からパーティクルボード等の構造用複合材の製造に使用
されているフェノール樹脂は、モノ・メチロール・フェ
ノールやジメチロール・フェノールが主体の低分子(数
平均分子量150前後)のレゾール型であるため、木質
小片中に含浸されやすく接着界面である木質小片表層の
樹脂量が少なくなる傾向にあり、従って構造用複合材と
しての強度を上げるためには使用する樹脂量を増加させ
る必要が生じ、コスト高となる不具合があった。しか
も、係る低分子のフェノール樹脂をバインダーとして使
用した場合、硬化した樹脂の硬度は有るがやや脆弱とな
る傾向があるため、構造用複合材としての強度が劣る不
具合があった。
2. Description of the Related Art Alkali resol type liquid phenol resins have been widely used as a binder for the production of this type of structural composite material. However, the phenolic resin that has been conventionally used for the production of structural composite materials such as particle board is a resol type of low molecular weight (number average molecular weight around 150) mainly composed of mono-methylol-phenol and dimethylol-phenol. Therefore, it tends to be impregnated into the wood chips and the amount of resin in the surface layer of the wood chips, which is the adhesive interface, tends to decrease.Therefore, it is necessary to increase the amount of resin used to increase the strength as a structural composite material. However, there was a problem that the cost was high. Moreover, when such a low molecular weight phenolic resin is used as a binder, the cured resin tends to be slightly fragile, but the strength of the structural composite material is poor.

【0003】[0003]

【発明が解決しようとする課題】本発明はこの様な従来
の不具合に鑑みてなされたものであり、レゾール型フェ
ノール樹脂の分子量を大きくして難水溶性とすることに
より、木質小片への含浸を抑えて接着界面である木質小
片表層の樹脂量が多くなるようにし、構造用複合材とし
ての強度を向上させることが出来る構造用複合材用バイ
ンダーを提供せんとするものである。
DISCLOSURE OF THE INVENTION The present invention has been made in view of such a conventional problem, and impregnates wood chips by increasing the molecular weight of the resol-type phenol resin to make it poorly water-soluble. It is intended to provide a binder for a structural composite material capable of suppressing the increase in the amount of resin in the surface layer of the small wood piece which is an adhesive interface and improving the strength of the structural composite material.

【0004】[0004]

【課題を解決するための手段】斯る目的を達成する本発
明の構造用複合材用バインダーは、フェノール1モルに
対してホルムアルデヒドを1〜2モル加えると共に、触
媒としてカセイソーダ0.05〜0.2モルとアンモニ
ア0.01〜0.1モルを加え、数平均分子量を300
〜600とした事を特徴としたものである。
The binder for structural composite material of the present invention which achieves the above object is obtained by adding 1 to 2 moles of formaldehyde to 1 mole of phenol and caustic soda 0.05 to 0. Add 2 mol and 0.01 to 0.1 mol of ammonia to give a number average molecular weight of 300.
It is characterized in that it is set to ~ 600.

【0005】[0005]

【実施例】以下、本発明の実施例を説明するが、本発明
はこれらの実施例に限定されるものではない。
EXAMPLES Examples of the present invention will be described below, but the present invention is not limited to these examples.

【0006】本発明に使用されるフェノールとしては、
市販されている通常の合成フェノールを用い、そのフェ
ノール1モルに対してホルムアルデヒドを1〜2モル加
えると共に、触媒としてカセイソーダ0.05〜0.2
モルとアンモニア0.01〜0.1モルを加えて反応さ
せる。
The phenol used in the present invention includes:
Using commercially available ordinary synthetic phenol, 1 to 2 mol of formaldehyde was added to 1 mol of the phenol, and caustic soda 0.05 to 0.2 as a catalyst.
Mol and 0.01 to 0.1 mol of ammonia are added and reacted.

【0007】又、本発明に使用されるホルムアルデヒド
としては、その水溶液である37%ホルマリンが好まし
く、重合物であるパラホルムアルデヒドを使用しても良
い。この場合、濃度の差と反応速度等を考慮して反応条
件を設定すれば充分目的を達成することができる。
As the formaldehyde used in the present invention, 37% formalin which is an aqueous solution thereof is preferable, and paraformaldehyde which is a polymer may be used. In this case, the purpose can be sufficiently achieved by setting the reaction conditions in consideration of the difference in concentration, the reaction rate, and the like.

【0008】ここで、フェノールに対するホルムアルデ
ヒドの量を、フェノール1モルに対して1〜2モルとす
ることが好ましい。何故なら、フェノール1モルに対し
てホルムアルデヒドの量が1モル以下では、木粉や木質
小片等のマトリックス材に混ぜ合わせて加熱加圧して成
形する際に硬化時間が長くなってしまい、2モル以上で
はホルムアルデヒド臭が強くなるだけでなく、残留ホル
ムアルデヒドが多くなるため加熱加圧して成形する際の
ガス発生量が多くなって構造用複合材としての強度が低
下してしまうからである。
It is preferable that the amount of formaldehyde with respect to phenol is 1 to 2 mol per mol of phenol. The reason is that if the amount of formaldehyde is 1 mol or less relative to 1 mol of phenol, the curing time becomes long when the mixture is mixed with a matrix material such as wood powder or wood chips and heated and pressed to form a mixture of 2 mol or more. In addition to the strong formaldehyde odor, the amount of residual formaldehyde increases, so that the amount of gas generated during heating and pressurizing and molding increases and the strength of the structural composite material decreases.

【0009】また、本発明では、触媒としてカセイソー
ダ0.05〜0.2モルとアンモニア0.01〜0.1
モルを加える。この場合、カセイソーダが0.05モル
以下では反応速度が遅く製造に時間がかかるため実用的
でなくなり、0.2モル以上では逆に反応が速すぎて分
子量の調整が困難となってしまう。同様に、アンモニア
が0.01モル以下では目的とする高分子量を得ること
が困難となり、0.1モル以上では高分子化が速すぎて
分子量の調整が困難となる。
Further, in the present invention, 0.05 to 0.2 mol of caustic soda and 0.01 to 0.1 of ammonia are used as catalysts.
Add moles. In this case, if the amount of caustic soda is less than 0.05 mol, the reaction rate will be slow and the production will take time, so that it will not be practical, and if it is more than 0.2 mol, the reaction will be too fast to control the molecular weight. Similarly, if the amount of ammonia is 0.01 mol or less, it will be difficult to obtain the desired high molecular weight, and if it is 0.1 mol or more, the polymerization will be too fast and the adjustment of the molecular weight will be difficult.

【0010】而して、本発明に係る構造用複合材用バイ
ンダーの製造に際しては、フェノール及びホルムアルデ
ヒドを夫々計量して撹拌機付で大気開放コンデンサーを
備えたステンレス製反応缶に投入し、撹拌しながら30
℃〜40℃に保持させ、次に上記反応缶の撹拌を継続さ
せながら所定量のカセイソーダ水溶液を徐々に加えて、
内温を45℃に保持させる。そして最後に、所定量のア
ンモニアを加えて、大気圧下において80℃〜100℃
に保ちながら1〜4時間反応させる。反応終了後、必要
に応じて、50℃〜60℃に保ちながら600〜750
mmHgに減圧して脱水濃縮し、固形分%を増加させる
ことができる。そうして、上記反応缶内の内容物を適量
採取し、25℃に急冷してその粘度を測定し、目標粘度
まで反応を継続させる。目標粘度に達したら、反応缶内
の内容物(バインダー)を35℃まで急冷させた後、所
定の容器に移す。
In the production of the structural composite binder according to the present invention, phenol and formaldehyde are weighed and charged into a stainless steel reaction can equipped with a stirrer and equipped with an atmosphere open condenser, and stirred. While 30
C. to 40.degree. C., and then a predetermined amount of caustic soda aqueous solution is gradually added while continuously stirring the reaction can,
The internal temperature is maintained at 45 ° C. And finally, a predetermined amount of ammonia is added, and at 80 ° C to 100 ° C under atmospheric pressure.
The reaction is carried out for 1 to 4 hours while maintaining the above. After completion of the reaction, if necessary, while maintaining the temperature at 50 ° C to 60 ° C, 600 to 750
The solid content can be increased by reducing the pressure to mmHg and dehydrating and concentrating. Then, an appropriate amount of the content in the reaction can is sampled, rapidly cooled to 25 ° C., the viscosity thereof is measured, and the reaction is continued to the target viscosity. When the target viscosity is reached, the contents (binder) in the reaction can are rapidly cooled to 35 ° C. and then transferred to a predetermined container.

【0011】次に、本発明の具体的な実施例を説明す
る。 [実施例1]市販されているフェノール1,000gと
37%ホルマリン1,290gを撹拌機と水冷式コンデ
ンサーを備えた3リットルの三ツ口フラスコに入れ、こ
れに40%カセイソーダ水溶液200gと25%アンモ
ニア水50gを触媒として加え、85℃〜95℃の湯浴
中にて加熱し、内温を90℃に保ちながら2時間反応さ
せた。然る後、常温まで冷却してレゾール型フェール樹
脂(バインダー)を2500g得た。
Next, specific examples of the present invention will be described. [Example 1] 1,000 g of commercially available phenol and 1,290 g of 37% formalin were placed in a 3 liter three-necked flask equipped with a stirrer and a water-cooled condenser, and 200 g of 40% caustic soda aqueous solution and 25% ammonia water were added to the flask. 50 g was added as a catalyst, and the mixture was heated in a hot water bath at 85 ° C to 95 ° C and allowed to react for 2 hours while keeping the internal temperature at 90 ° C. Then, the mixture was cooled to room temperature to obtain 2500 g of resol type fail resin (binder).

【0012】[実施例2]前記実施例1と同じ配合割合
のものを同じ条件で反応させた後、内温を50℃〜60
℃に保ちながらアスピレーターで600〜750mmH
gに減圧して内部の水分を沸騰溜出させ、15分間脱水
濃縮してレゾール型フェール樹脂(バインダー)を23
00g得た。
Example 2 After reacting the same proportion as in Example 1 under the same conditions, the internal temperature was 50 ° C. to 60 ° C.
600-750mmH with an aspirator while keeping at ℃
Reduce the pressure to g to evaporate the internal water by boiling, and dehydrate and concentrate for 15 minutes to remove the resol-type fail resin (binder) to 23
00g was obtained.

【0013】次に、本発明に係る構造用複合材用バイン
ダーの性能を確めるために、板材を成形した。即ち、自
動車用タイヤ(の廃材)を粉砕機で粒径2ミリ以下に粉
砕してなる加硫ゴムチップ500gと、直径2ミリ以
下,長さ6ミリ以下に破砕した松材チップ1,000g
とを混ぜ合わせ、これに前記実施例1並びに実施例2で
作成したバインダーを各々固形分換算で200g加え
て、品川式混合機で4分間混合した。次いで、この混合
物を80℃〜100℃の熱風で15分間乾燥して、水分
を8〜12%に調整した後、150℃に加熱せしめた金
型に入れ、35kg/cm2 の圧力で10分間加圧し
て、長さ200ミリ,幅200ミリ,厚さ15ミリの板
材を成形した。
Next, in order to confirm the performance of the binder for structural composite material according to the present invention, a plate material was formed. That is, 500 g of vulcanized rubber chips obtained by crushing (waste materials of) automobile tires with a crusher to a particle size of 2 mm or less and pine wood chips of 1000 g crushed to a diameter of 2 mm or less and a length of 6 mm or less.
Were mixed, and 200 g of each of the binders prepared in Example 1 and Example 2 was added in terms of solid content, and mixed for 4 minutes with a Shinagawa mixer. Then, this mixture is dried with hot air of 80 ° C to 100 ° C for 15 minutes to adjust the water content to 8 to 12%, and then placed in a mold heated to 150 ° C, and at a pressure of 35 kg / cm 2 for 10 minutes. By pressing, a plate material having a length of 200 mm, a width of 200 mm, and a thickness of 15 mm was formed.

【0014】[比較例]比較のために、市販フェノール
1,000gに37%ホルマリン1,290gと40%
カセイソーダ水溶液200gを加えて、前記実施例1で
使用した反応装置を用いて内温65℃で2時間反応さ
せ、レゾール型フェノール樹脂を得た。そして、得られ
たフェノール樹脂を用いて前記と同様の条件で同じ大き
さの板材を成形した。
Comparative Example For comparison, 1,000 g of commercially available phenol, 37% formalin, 1,290 g and 40% were added.
200 g of an aqueous caustic soda solution was added, and the reaction was performed at the internal temperature of 65 ° C. for 2 hours using the reaction apparatus used in Example 1 to obtain a resol-type phenol resin. Then, using the obtained phenol resin, a plate material having the same size was formed under the same conditions as above.

【0015】斯くして、前記実施例1及び実施例2と比
較例で得られた構造用複合材用バインダー(フェノール
樹脂)の性状を表1に、そして前記実施例1及び実施例
2と比較例で得られたバインダー(フェノール樹脂)を
用いて成形した各板材について物性値を測定した結果を
表2に、夫々まとめて示す。
Thus, the properties of the structural composite binder (phenolic resin) obtained in Examples 1 and 2 and Comparative Example are shown in Table 1 and compared with those of Examples 1 and 2. Table 2 shows the results of measuring the physical properties of each plate material molded using the binder (phenol resin) obtained in the example.

【0016】[0016]

【表1】 [Table 1]

【0017】上記の表1に示したデータから解るよう
に、実施例1及び実施例2に係るバインダーの粘度が比
較例と比較して桁違いに高く、数平均分子量は比較例の
約3.5倍程高分子となっている。
As can be seen from the data shown in Table 1 above, the viscosities of the binders of Examples 1 and 2 are orders of magnitude higher than those of Comparative Examples, and the number average molecular weight is about 3. It is about 5 times more polymer.

【0018】[0018]

【表2】 [Table 2]

【0019】上記の表2に示した結果では、実施例1及
び実施例2のものの方が比較例のものと比較して、曲げ
強さ並びに曲げヤング率が20%以上も向上しているこ
とが理解される。また、板材の木質小片表面を肉眼で観
察したところ、実施例1及び実施例2のものは比較例の
ものよりも樹脂量が多いように見えた。
From the results shown in Table 2 above, the bending strength and bending Young's modulus of Examples 1 and 2 are improved by 20% or more as compared with those of Comparative Example. Is understood. Further, when the surface of the wooden piece of the plate material was observed with the naked eye, the resin of Examples 1 and 2 seemed to have a larger amount of resin than the resin of Comparative Example.

【0020】[0020]

【発明の効果】本発明に係る構造用複合材用バインダー
は斯様に、従来のこの種バインダーよりも分子量が2〜
4倍程大きく難水溶性とすることにより、木質小片への
含浸を抑えて接着界面である木質小片表層の樹脂量が多
くなって、構造用複合材を製造する際に、加熱加圧成形
時にマトリックス材との密着性が良くなり、その結果、
構造用複合材用のバインダーとして強度を向上させるこ
とができる。
The binder for structural composite materials according to the present invention thus has a molecular weight of 2 to 2 as compared with the conventional binders of this kind.
By making it about 4 times as large as water-insoluble, the amount of resin in the surface layer of the wood chips, which is the adhesive interface, is suppressed by suppressing the impregnation into the wood chips, and when heat-press molding is performed during the production of the structural composite material. Adhesion with the matrix material is improved, and as a result,
Strength can be improved as a binder for structural composite materials.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 フェノール1モルに対してホルムアル
デヒドを1〜2モル加えると共に、触媒としてカセイソ
ーダ0.05〜0.2モルとアンモニア0.01〜0.
1モルを加え、数平均分子量を300〜600としてな
る事を特徴とする構造用複合材用バインダー。
1. Addition of 1 to 2 mol of formaldehyde to 1 mol of phenol, 0.05 to 0.2 mol of caustic soda as catalyst and 0.01 to 0.
A binder for structural composite material, wherein 1 mol is added and the number average molecular weight is 300 to 600.
JP27115294A 1994-11-04 1994-11-04 Binder for structural composite Pending JPH08134424A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP27115294A JPH08134424A (en) 1994-11-04 1994-11-04 Binder for structural composite

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27115294A JPH08134424A (en) 1994-11-04 1994-11-04 Binder for structural composite

Publications (1)

Publication Number Publication Date
JPH08134424A true JPH08134424A (en) 1996-05-28

Family

ID=17496064

Family Applications (1)

Application Number Title Priority Date Filing Date
JP27115294A Pending JPH08134424A (en) 1994-11-04 1994-11-04 Binder for structural composite

Country Status (1)

Country Link
JP (1) JPH08134424A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009084467A (en) * 2007-10-01 2009-04-23 Aica Kogyo Co Ltd Adhesive composition suitable for two-part separate coating use, and method for producing laminated form using the same, and the resultant laminated form
JP2010208133A (en) * 2009-03-10 2010-09-24 Dic Corp Method of manufacturing high-strength particle board

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009084467A (en) * 2007-10-01 2009-04-23 Aica Kogyo Co Ltd Adhesive composition suitable for two-part separate coating use, and method for producing laminated form using the same, and the resultant laminated form
JP2010208133A (en) * 2009-03-10 2010-09-24 Dic Corp Method of manufacturing high-strength particle board

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