JPH0631708A - Light-weight particle board - Google Patents
Light-weight particle boardInfo
- Publication number
- JPH0631708A JPH0631708A JP21566692A JP21566692A JPH0631708A JP H0631708 A JPH0631708 A JP H0631708A JP 21566692 A JP21566692 A JP 21566692A JP 21566692 A JP21566692 A JP 21566692A JP H0631708 A JPH0631708 A JP H0631708A
- Authority
- JP
- Japan
- Prior art keywords
- particle board
- synthetic resin
- specific gravity
- weight
- less
- 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
- 239000002245 particle Substances 0.000 title claims abstract description 95
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 37
- 239000000057 synthetic resin Substances 0.000 claims abstract description 37
- 230000005484 gravity Effects 0.000 claims abstract description 29
- 230000006835 compression Effects 0.000 claims abstract description 15
- 238000007906 compression Methods 0.000 claims abstract description 15
- 239000006260 foam Substances 0.000 claims description 31
- 239000002023 wood Substances 0.000 claims description 20
- 239000004793 Polystyrene Substances 0.000 claims description 4
- 229920002223 polystyrene Polymers 0.000 claims description 4
- 238000005452 bending Methods 0.000 abstract description 13
- 239000000203 mixture Substances 0.000 abstract description 5
- 239000010410 layer Substances 0.000 description 14
- 239000000853 adhesive Substances 0.000 description 11
- 230000001070 adhesive effect Effects 0.000 description 11
- 239000002344 surface layer Substances 0.000 description 10
- 238000005187 foaming Methods 0.000 description 8
- 238000007731 hot pressing Methods 0.000 description 8
- 239000011324 bead Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 5
- 229920001807 Urea-formaldehyde Polymers 0.000 description 5
- -1 isocyanate compound Chemical class 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000013585 weight reducing agent Substances 0.000 description 4
- 241000218645 Cedrus Species 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920006248 expandable polystyrene Polymers 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- 239000004566 building material Substances 0.000 description 2
- 239000004794 expanded polystyrene Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000012856 packing Methods 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- 241000208140 Acer Species 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 240000007182 Ochroma pyramidale Species 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 240000002871 Tectona grandis Species 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 230000006837 decompression Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000010097 foam moulding Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Landscapes
- Dry Formation Of Fiberboard And The Like (AREA)
- Laminated Bodies (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は建築材料および家具材料
等の使用に好適な密度が0.5g/cm3 以下の軽量パーテ
ィクルボードに関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a lightweight particle board having a density of 0.5 g / cm3 or less, which is suitable for use in building materials and furniture materials.
【0002】[0002]
【従来の技術】木材チップから製造されるパーティクル
ボードは、木材資源の利用度が高いこと、均一な長大製
品の製造が可能なこと等の特徴があり建築材料、家具材
料等広範に利用されている。しかしながら、一般に市販
されているパーティクルボードは高比重で重く、実用上
作業性に欠けるという問題があった。低比重のパーティ
クルボードは原理的には木質チップの使用重量を減少さ
せることによって容易に製造できるが、曲げ強度、剥離
強度が大幅に低下するので実用的ではなかった。2. Description of the Related Art Particleboard manufactured from wood chips is characterized by high utilization of wood resources and the ability to manufacture uniform long products, and is widely used in building materials, furniture materials, etc. There is. However, generally commercially available particle boards have a high specific gravity and are heavy, and there is a problem in that they lack practical workability. In principle, a low specific gravity particle board can be easily manufactured by reducing the weight of wood chips used, but it is not practical because the bending strength and peeling strength are significantly reduced.
【0003】これらの欠点を改良するものとして、例え
ばチップに熱可塑性樹脂を塗布し、その上に更に熱硬化
性樹脂接着剤を塗布後、熱圧して接着剤のチップへの浸
透を抑えて剥離強度を高める方法(特公昭58−411
92号公報)が提案されている。しかしながら、この方
法はボードの軽量化と剥離強度の改善には効果があるが
曲げ強度は十分とはいえないものであった。また、含水
チップと水発泡性のウレタン系樹脂を使用し、樹脂が硬
化する前に解圧して所定の厚みに発泡成形する方法(特
公昭61−3678号公報)、揮発性液体を内蔵する熱
可塑性合成樹脂カプセルを混合する方法(特公平3−3
1567号公報)等が提案されている。これらは、いず
れも熱圧成形中に内部で発泡させて軽量化をはかるもの
であるが、前者は樹脂の硬化速度が含水率の大小、温度
差、木質チップの差や木質チップに混在する不純物など
により影響を受けやすく、得られたパーティクルボード
の厚みや密度のばらつきが大きくなり、後者は発泡状態
が不均一になりやすく、解圧後の厚みのもどりが著しい
ため、表面の平滑性が損なわれやすいという欠点を有す
る。In order to improve these drawbacks, for example, a chip is coated with a thermoplastic resin, a thermosetting resin adhesive is further applied thereon, and then hot pressing is performed to prevent the adhesive from penetrating into the chip and peeling. Method to increase strength (Japanese Patent Publication No. 58-411)
No. 92) is proposed. However, this method was effective in reducing the weight of the board and improving the peel strength, but the bending strength was not sufficient. Further, a method of using a water-containing chip and a water-foaming urethane resin, decompressing the resin to cure it and foam-molding it to a predetermined thickness (Japanese Patent Publication No. 61-3678), heat containing a volatile liquid. Method of mixing plastic synthetic resin capsules (Japanese Patent Publication No. 3-3
No. 1567) has been proposed. All of these are intended to reduce the weight by foaming inside during thermocompression molding, but the former is such that the curing rate of the resin is high or low in water content, temperature difference, difference in wood chips or impurities mixed in wood chips. The resulting particle board has a large variation in the thickness and density of the particle board, and the latter tends to have a non-uniform foaming state, and the thickness of the particle board after the depressurization remarkably decreases, resulting in impaired surface smoothness. It has the drawback of being easily damaged.
【0004】一方、チップに合成樹脂発泡体又は軽量充
填材を混合してなる低比重ボード(実公昭57−593
25号公報、実開昭61−74406号公報)も提案さ
れているが、合成樹脂発泡体や軽量充填材は熱圧成形時
の圧力で変形しやすく、その場合解圧すると厚みもどり
を生じたり、表面の平滑性が損なわれやすかった。ま
た、木質チップに比べて部分的な圧締不足が生じやすく
所望の曲げ強度が得られないという問題点もあった。On the other hand, a low specific gravity board formed by mixing a chip with a synthetic resin foam or a lightweight filler (Jitsuko Sho 57-593).
No. 25 and Japanese Utility Model Laid-Open No. 61-74406) have been proposed, but synthetic resin foams and lightweight fillers are easily deformed by the pressure during thermocompression molding. The surface smoothness was easily impaired. Further, there is also a problem that a desired bending strength cannot be obtained because partial insufficient clamping tends to occur as compared with a wood chip.
【0005】[0005]
【発明が解決しようとする課題】本発明は、実用上なん
ら問題ない曲げ強度、剥離強度を有しかつ密度0.5g/
cm3 以下の低密度な軽量パーティクルボードを提供する
ものである。DISCLOSURE OF THE INVENTION The present invention has a bending strength and a peeling strength with no practical problems and has a density of 0.5 g /
It provides lightweight particle board with low density of less than cm3.
【0006】[0006]
【課題を解決するための手段】本発明によれば、3層パ
ーティクルボードの中層が、木質チップ100重量部及
び見かけ比重が0.3以下、圧縮弾性率が30kg/cm2以
上の合成樹脂発泡粒5〜30重量部からなることを特徴
とする軽量パーティクルボードが提供され、更に、比重
が0.5未満の木質チップを使用することを特徴とする
前記軽量パーティクルボードが提供され、更にまた、前
記合成樹脂発泡粒がポリスチレンよりなることを特徴と
する前記軽量パーティクルボードが提供される。According to the present invention, the middle layer of three-layer particle board has 100 parts by weight of wood chips, an apparent specific gravity of 0.3 or less, and a compression modulus of 30 kg / cm 2 or more of synthetic resin foam particles. There is provided a lightweight particle board characterized by comprising 5 to 30 parts by weight, and further provided is the lightweight particle board characterized by using a wood chip having a specific gravity of less than 0.5. There is provided the lightweight particle board, wherein the synthetic resin foam particles are made of polystyrene.
【0007】即ち、木質チップと見かけ比重が0.3以
下、圧縮弾性率が30kg/cm2以上の合成樹脂発泡粒の混
合物をパーティクルボードの中層に使用すると熱圧時の
圧締不足や熱圧後の厚みもどり、あるいは表面の平滑性
が悪くなること等がない機械的強度に優れた密度0.5
g/cm3 以下のパーティクルボードが得られることを見い
だした。That is, when a mixture of wood chips and synthetic resin foam particles having an apparent specific gravity of 0.3 or less and a compression elastic modulus of 30 kg / cm 2 or more is used for the middle layer of the particle board, insufficient compression during hot pressing or after hot pressing The density is 0.5, which has excellent mechanical strength and does not cause the thickness of the product to return or the surface smoothness to deteriorate.
It was found that a particle board of g / cm3 or less can be obtained.
【0008】本発明の軽量パーティクルボードに用いる
木質チップとしては、通常供給される木質チップが制限
なく使用できるが、例えば比重が0.5を超えるラワ
ン、カポール、マカンバ、チーク、アピトン、カエデな
ど、及び比重が0.5未満の杉、ファルカタ、バルサな
どのチップが挙げられ、これらは混合チップとして使用
されるのが一般的である。特に、杉、ファルカタ等比重
が0.5未満の比較的低比重の樹木よりなるチップを使
用するのが曲げ強度等の機械的強度を高くする上で好ま
しい。また、これらのチップは細かいチップと荒いチッ
プに分級して、細かいチップは表層に、荒いチップは中
層に使用するのが望ましい。As the wood chips used in the lightweight particle board of the present invention, wood chips that are normally supplied can be used without limitation, but for example, Lauan, Kapole, Macamba, Teak, Apito, maple, etc. having a specific gravity of more than 0.5 can be used. And chips such as cedar, falcata, and balsa having a specific gravity of less than 0.5, which are generally used as mixed chips. In particular, it is preferable to use a chip made of a tree having a relatively low specific gravity such as cedar or falcata having a specific gravity of less than 0.5 in order to increase mechanical strength such as bending strength. Further, it is desirable to classify these chips into fine chips and rough chips, and use the fine chips in the surface layer and the rough chips in the middle layer.
【0009】接着剤としてはフェノール樹脂、ユリア−
メラミン樹脂、ユリア樹脂、多官能性イソシアネート化
合物系接着剤等パーティクルボードの製造に通常使用す
る接着剤がそのままなんら限定することなく使用でき
る。As the adhesive, phenol resin, urea-
Adhesives usually used for producing particle boards such as melamine resins, urea resins, and polyfunctional isocyanate compound-based adhesives can be used as they are without any limitation.
【0010】見かけ比重が0.3以下、圧縮弾性率が3
0kg/cm2以上の合成樹脂発泡粒としては、ポリスチレ
ン、ポリエチレン、ポリプロピレン、塩化ビニル樹脂、
アクリル樹脂、ナイロン等の熱可塑性樹脂及びウレタン
樹脂、フェノール樹脂、尿素樹脂、エポキシ樹脂、シリ
コーン樹脂等の熱硬化性樹脂の発泡粒が挙げられる。合
成樹脂発泡粒の見かけ比重が0.3を超えるとパーティ
クルボードの軽量化にほとんど効果がなく、一方合成樹
脂発泡粒の見かけ比重が低いと軽量化には効果的である
が、あまり低いと圧縮弾性率も低く、熱圧成形時の圧力
によって該発泡粒が変形して厚みもどりを生じたり、破
壊して圧締不足を生じたりして所望の物性が得られなく
なる。したがって、合成樹脂の種類にもよるが見かけ比
重は0.02〜0.3が好ましく、0.05〜0.3が
特に好ましい。また、圧縮弾性率が30kg/cm2未満の場
合も熱圧成形時に発泡粒が変形して圧締不足となり曲げ
強度などが低下するので好ましくない。したがって、上
記見かけ比重と圧縮弾性率を同時に満たす合成樹脂発泡
粒を使用することが必要である。一般に合成樹脂発泡粒
の発泡倍率は4〜50倍が選択される。Apparent specific gravity is 0.3 or less, compression elastic modulus is 3
The synthetic resin foam particles of 0 kg / cm2 or more include polystyrene, polyethylene, polypropylene, vinyl chloride resin,
Examples include thermoplastic resin such as acrylic resin and nylon, and foamed particles of thermosetting resin such as urethane resin, phenol resin, urea resin, epoxy resin and silicone resin. If the apparent specific gravity of the synthetic resin foam particles exceeds 0.3, there is little effect on weight reduction of the particle board, while if the apparent specific gravity of the synthetic resin foam particles is low, it is effective for weight reduction, but if it is too low, compression occurs. The elastic modulus is also low, and the foamed particles are deformed by the pressure at the time of thermocompression to cause a thickness reversion, or they are broken to cause insufficient compression and the desired physical properties cannot be obtained. Therefore, the apparent specific gravity is preferably 0.02 to 0.3, and particularly preferably 0.05 to 0.3, though it depends on the kind of the synthetic resin. Also, if the compressive elastic modulus is less than 30 kg / cm @ 2, the foamed particles are deformed during thermocompression molding, resulting in insufficient compression and bending strength, etc., which is not preferable. Therefore, it is necessary to use synthetic resin foam particles that simultaneously satisfy the apparent specific gravity and the compression elastic modulus. Generally, the expansion ratio of synthetic resin foam particles is selected to be 4 to 50 times.
【0011】本発明においては、ポリスチレンよりなる
合成樹脂発泡粒が常温において硬質であり、吸水率、透
湿率が小さいこと、軟化温度が75〜90℃と低いので
熱圧圧締時に木質チップが接触している部分は充分に軟
化し、木質チップ表面の凹部へ浸透し、熱融着すること
から物理的に木質チップとの固着力に優れていること、
更に独立発泡構造により高度な断熱性能を有するため発
泡粒の内部まで軟化、溶融することなく独立発泡構造を
維持できること等の利点を有し曲げ強度、剥離強度、木
ねじ保持力などの各強度が比較的高強度に発現するので
特に好ましい。In the present invention, the synthetic resin foam particles made of polystyrene are hard at room temperature, have a low water absorption rate and a low moisture permeability, and the softening temperature is as low as 75 to 90 ° C., so that the wood chips come into contact with each other during hot pressing. The part that is softened sufficiently penetrates into the concave part of the wood chip surface, and because it is heat-sealed, it has excellent physical adhesion with the wood chip,
In addition, since it has a high degree of heat insulation performance due to the independent foam structure, it has the advantage that it can maintain the independent foam structure without softening and melting even inside the foamed granules.Comparing each strength such as bending strength, peeling strength, wood screw holding power, etc. It is particularly preferable because it is expressed with extremely high strength.
【0012】上記合成樹脂発泡粒は市販の発泡性ビーズ
を加熱発泡処理してから使用するか、又はフォーム状の
発泡体を粉砕、破砕して使用することができる。発泡性
ビーズ、例えば発泡性ポリスチレンビーズは100〜1
20℃、10〜30分加熱発泡し完全発泡状態とした
後、放冷にて熟成、養生して使用される。発泡条件が1
00℃、10分以下の時は完全発泡していないので、熱
圧圧締した後に発泡して厚みのもどりが生じて表面の平
滑性が損なわれたり強度低下を招きやすく、発泡条件が
120℃、30分以上の時は、過熱発泡状態となり該発
泡性ポリスチレンビーズ中のペンタン、ヘキサン、ヘプ
タンなどの揮発性発泡剤が揮発し、収縮するため、所望
の軽量化が得られないので好ましくない。The above-mentioned synthetic resin expanded beads can be used after heat-expanding commercially available expandable beads, or can be used by crushing and crushing a foam-like foam. 100 to 1 for expandable beads, for example expandable polystyrene beads
After heat-foaming at 20 ° C. for 10 to 30 minutes to obtain a completely foamed state, it is aged and cured by allowing it to cool. Foaming condition is 1
Since it is not completely foamed at 00 ° C for 10 minutes or less, foaming occurs after hot-pressing to cause a thickness reversion, which tends to impair the surface smoothness or reduce the strength. When it is more than 30 minutes, it is in an overheated foaming state and the volatile foaming agent such as pentane, hexane, heptane in the expandable polystyrene beads volatilizes and shrinks, so that the desired weight reduction cannot be obtained, which is not preferable.
【0013】本発明の軽量パーティクルボードは例えば
以下の方法で製造される。まず、木質チップを細かいチ
ップと荒いチップに分級して、細かいチップを表層に用
いる。一方、荒いチップは該チップ100重量部に対し
て5〜30重量部の上記合成樹脂発泡粒と混合して中層
に用いる。合成樹脂発泡粒の配合量が5重量部未満の場
合、軽量化効果がほとんどなく、30重量部を超えると
中層中の合成樹脂発泡粒の占める体積が大きくなりすぎ
て安定した熱圧ができなくなるので好ましくない。これ
らのチップ及びチップと合成樹脂発泡粒の混合物に上記
した接着剤を通常の方法で塗布し、熱圧成形する。熱圧
条件は合成樹脂発泡粒の添加量、見かけ比重、接着剤の
種類等に応じて調節すべきであるが、例えばユリア樹脂
を接着剤として用いた場合は140〜160℃、フェノ
ール樹脂の場合には180〜200℃の温度で、圧力1
0〜35kg/cm2の範囲で熱圧圧締を行う。ついで、得ら
れた板状物の表面をベルトサンダー、プレーナーなどの
研削機械によりプレキュア状態の結合力の弱い表面層の
除去を行い、表面を平滑に研磨することにより本発明の
軽量パーティクルボードが得られる。The lightweight particle board of the present invention is manufactured, for example, by the following method. First, the wood chips are classified into fine chips and rough chips, and the fine chips are used for the surface layer. On the other hand, the rough chip is mixed with 5 to 30 parts by weight of the synthetic resin foam particles with respect to 100 parts by weight of the chip and used as an intermediate layer. When the compounded amount of the synthetic resin foamed particles is less than 5 parts by weight, there is almost no weight reduction effect, and when it exceeds 30 parts by weight, the volume occupied by the synthetic resin foamed particles in the middle layer becomes too large and stable heat pressing cannot be performed. It is not preferable. The above-mentioned adhesive is applied to these chips and a mixture of the chips and the foamed synthetic resin particles by a usual method, and thermocompression molding is performed. The heat and pressure conditions should be adjusted depending on the amount of synthetic resin foam particles added, the apparent specific gravity, the type of adhesive, etc. For example, when urea resin is used as the adhesive, 140 to 160 ° C. At a temperature of 180-200 ° C and a pressure of 1
Hot pressing is performed in the range of 0 to 35 kg / cm2. Then, the surface layer of the obtained plate-like material is removed by a grinding machine such as a belt sander or a planer to remove the surface layer having a weak bonding force in a pre-cure state, and the surface is polished to obtain a lightweight particle board of the present invention. To be
【0014】[0014]
【作用】図1に示したように、このようにして得られる
本発明の軽量パーチィクルボード1は中層部分3に木質
チップ5と内部が中空で見かけ比重の小さい合成樹脂発
泡粒4を有しているので軽量で、また該合成樹脂発泡粒
4の圧縮弾性率が高いため十分な圧締が可能となる。し
たがって表層部2が十分圧縮されるので曲げ強度、剥離
強度等の機械的強度を発揮できるのである。また、圧締
時に合成樹脂発泡粒4があまり変形しないので解圧後の
厚みもどりもなく平滑な表面のパーティクルボード1が
得られる。As shown in FIG. 1, the thus obtained lightweight particle board 1 of the present invention has a wood chip 5 in the middle layer portion 3 and a synthetic resin foam particle 4 having a hollow inside and a small apparent specific gravity. Therefore, the synthetic resin foam particles 4 have a high compression elastic modulus and can be sufficiently compressed. Therefore, since the surface layer portion 2 is sufficiently compressed, mechanical strength such as bending strength and peeling strength can be exhibited. Further, since the synthetic resin foam particles 4 do not deform so much at the time of compression, the particle board 1 having a smooth surface with no thickness after decompression can be obtained.
【0015】[0015]
【実施例】以下実施例により、本発明を更に詳しく説明
する。なお、実施例中の密度、曲げ強度、剥離強度はJ
IS−A5908に準拠して測定した。また、使用した
原材料は以下の通りである。 <表層用接着剤> ユリア樹脂 100.0重量部 20% 塩化アンモニウム水溶液 0.2重量部 25% アンモニア水溶液 0.2重量部 水 10.0重量部 <中層用接着剤> ユリア樹脂 100.0重量部 20% 塩化アンモニウム水溶液 3.0重量部 25% アンモニア水溶液 0.5重量部The present invention will be described in more detail with reference to the following examples. The density, bending strength, and peel strength in the examples are J
It was measured according to IS-A5908. The raw materials used are as follows. <Adhesive for surface layer> Urea resin 100.0 parts by weight 20% Ammonium chloride aqueous solution 0.2 parts by weight 25% Aqueous ammonia solution 0.2 parts by weight Water 10.0 parts by weight <Adhesive for middle layer> Urea resin 100.0 parts by weight 20% ammonium chloride aqueous solution 3.0 parts by weight 25% ammoniacal aqueous solution 0.5 parts by weight
【0016】参考例1 発泡倍率20倍のポリスチレンの発泡性ビーズを110
℃で18分処理して粒径3〜5mmの完全発泡した合成
樹脂発泡粒Aを得た。この発泡粒の見かけ比重は0.0
5、圧縮弾性率は38kg/cm2であった。Reference Example 1 110 expandable polystyrene beads having an expansion ratio of 20 were used.
Treatment at 18 ° C. for 18 minutes gave fully foamed synthetic resin foam particles A having a particle size of 3 to 5 mm. The apparent specific gravity of these foamed particles is 0.0
5, the compression elastic modulus was 38 kg / cm 2.
【0017】実施例1、2及び比較例1、2 比重が0.5未満の杉、ファルカタをフレーカー、リフ
ァイナー等の粉砕機で粉砕して得られた混合チップを分
級して細かいチップを表層に、荒いチップは中層に使用
することとした。ついで、荒いチップ100重量部に対
して参考例1で得られた合成樹脂発泡粒Aを表1に示す
量(単位:重量部)配合して混合し、表層用チップ及び
中層用混合物に接着剤をそれぞれ200g/m2塗布して、
設定密度が0.45(表層:中層は重量比で1:1)に
なるように秤量した後、フォーミングしてから160℃
で5分間、25kg/cm2の圧力で熱圧圧締することにより
パーティクルボードを製造した。得られたパーティクル
ボードの諸性質を同じく表1に示す。Examples 1 and 2 and Comparative Examples 1 and 2 Mixed chips obtained by crushing cedar and falcata having a specific gravity of less than 0.5 with a crusher such as a flaker or a refiner are classified to form fine chips on the surface layer. , Decided to use rough chips for the middle layer. Next, 100 parts by weight of the rough chips were mixed with the synthetic resin foam particles A obtained in Reference Example 1 in an amount (unit: parts by weight) shown in Table 1 and mixed to form an adhesive for the surface layer chips and the intermediate layer mixture. 200g / m2 each,
After weighing so that the set density is 0.45 (weight ratio of surface layer: middle layer is 1: 1), after forming, 160 ° C.
A particle board was manufactured by hot pressing at a pressure of 25 kg / cm @ 2 for 5 minutes. Various properties of the obtained particle board are also shown in Table 1.
【0018】[0018]
【表1】 [Table 1]
【0019】実施例3 比重が0.6を超えるラワン、カポールのチップの混合
物を使用した以外は実施例1と同様にしてパーティクル
ボードを製造した。得られたパーティクルボードの密度
は0.45g/cm3 であり、曲げ強度110.5kg/cm2、
剥離強度3.7kg/cm2と十分な機械的強度を示した。ま
た外観は良好で表面の凹凸はなかった。Example 3 A particle board was manufactured in the same manner as in Example 1 except that a mixture of chips of Lauan and Kapole having a specific gravity of more than 0.6 was used. The density of the obtained particle board is 0.45 g / cm3, the bending strength is 110.5 kg / cm2,
The peel strength was 3.7 kg / cm @ 2, which was a sufficient mechanical strength. The appearance was good and there were no surface irregularities.
【0020】比較例3 合成樹脂発泡粒を使用しない以外は実施例1と同様にし
てパーティクルボードを製造した。得られたパーティク
ルボードの諸性質を表2に示す。表2からも明らかなよ
うに合成樹脂発泡粒を用いずに製造した低比重のパーテ
ィクルボードの機械的強度は曲げ、剥離強度がいずれも
低く実用上不十分であった。Comparative Example 3 A particle board was manufactured in the same manner as in Example 1 except that synthetic resin foam particles were not used. Table 2 shows various properties of the obtained particle board. As is clear from Table 2, the mechanical strength of the particle board having a low specific gravity produced without using the synthetic resin foamed particles was low in both bending and peeling strength and was not practically sufficient.
【0021】比較例4 合成樹脂発泡粒を使用しない以外は実施例3と同様にし
てパーティクルボードを製造した。得られたパーティク
ルボードの諸性質を表2に示す。表2からも明らかなよ
うに合成樹脂発泡粒を用いずに製造した低比重のパーテ
ィクルボードの機械的強度は曲げ、剥離強度がいずれも
低く実用上不十分であった。Comparative Example 4 A particle board was manufactured in the same manner as in Example 3 except that synthetic resin foam particles were not used. Table 2 shows various properties of the obtained particle board. As is clear from Table 2, the mechanical strength of the particle board having a low specific gravity produced without using the synthetic resin foamed particles was low in both bending and peeling strength and was not practically sufficient.
【0022】[0022]
【表2】 [Table 2]
【0023】参考例2 緩衝材として使用されていた発泡ポリスチレンを粉砕機
で粉砕して粒径3〜5mmの合成樹脂発泡粒Bを得た。
この発泡粒の見かけ比重は0.02、圧縮弾性率は1
5.2kg/cm2であった。Reference Example 2 Expanded polystyrene used as a cushioning material was crushed by a crusher to obtain synthetic resin foamed particles B having a particle size of 3 to 5 mm.
The apparent specific gravity of the foamed particles is 0.02, and the compression elastic modulus is 1.
It was 5.2 kg / cm2.
【0024】比較例5 参考例2で得られた合成樹脂発泡粒Bを20重量部使用
した以外は実施例1と同様にしてパーティクルボードを
製造したが、熱圧圧締後の厚みもどりが大きくパンク状
態となって諸性質の測定はできなかった。Comparative Example 5 A particle board was produced in the same manner as in Example 1 except that 20 parts by weight of the synthetic resin foam particles B obtained in Reference Example 2 were used, but the thickness after hot pressing was large and the puncture was large. In this state, various properties could not be measured.
【0025】参考例3 ジフェニルメタンジイソシアネート(日本ポリウレタン
工業製、商品名MR−100)87重量部とポリオール
(日本ポリウレタン製、商品名DRN−1202)10
0重量部をラボミキサーで5000〜6000rpm/mi
n.、10分間攪拌混合して見かけ比重0.25の発泡ウ
レタンフォームを得た。これを粉砕機で粉砕して粒径
0.3〜5.0mmの合成樹脂発泡粒Cを得た。この発
泡粒の圧縮弾性率は133.5kg/cm2であった。Reference Example 3 87 parts by weight of diphenylmethane diisocyanate (manufactured by Nippon Polyurethane Industry, trade name MR-100) and polyol (manufactured by Nippon Polyurethane, trade name DRN-1202) 10
0 part by weight with a lab mixer 5000-6000 rpm / mi
n. Stir-mixed for 10 minutes to obtain a urethane foam having an apparent specific gravity of 0.25. This was crushed with a crusher to obtain synthetic resin foam particles C having a particle size of 0.3 to 5.0 mm. The compression modulus of the foamed granules was 133.5 kg / cm 2.
【0026】実施例4 参考例3で得られた合成樹脂発泡粒Cを20重量部使用
した以外は実施例1と同様にしてパーティクルボードを
製造した。得られたパーティクルボードの密度は0.4
1g/cm3 であり、機械的強度は曲げ強度が157.2kg
/cm2、剥離強度が5.2kg/cm2と良好であった。また、
熱圧成形時の圧締不足、熱圧成形後の厚みもどりもなく
外観も良好であった。Example 4 A particle board was manufactured in the same manner as in Example 1 except that 20 parts by weight of the synthetic resin foam particles C obtained in Reference Example 3 were used. The density of the obtained particle board is 0.4
1g / cm3, mechanical strength is flexural strength 157.2kg
/ cm2, peel strength was as good as 5.2 kg / cm2. Also,
The appearance was good with no insufficient tightening during hot-press forming and no thickness after hot-press forming.
【0027】参考例4 発泡倍率20倍の発泡性ポリエチレンビーズを140℃
で約20分間加熱して完全発泡させた後、一晩放冷して
熟成、養生して粒径3〜5mmの発泡ポリエチレン粒D
を得た。この発泡粒の見かけ比重は0.03、圧縮弾性
率は48.3kg/cm2であった。Reference Example 4 Expandable polyethylene beads having an expansion ratio of 20 times are placed at 140 ° C.
After heating for about 20 minutes to complete foaming, let it cool overnight, age and cure, and foam polyethylene particles D with a particle size of 3-5 mm.
Got The apparent specific gravity of the foamed particles was 0.03, and the compressive elastic modulus was 48.3 kg / cm 2.
【0028】実施例5 参考例4で得られた合成樹脂発泡粒Dを10重量部使用
した以外は実施例1と同様にしてパーティクルボードを
製造した。得られたパーティクルボードの密度は0.4
3g/cm3 であり、機械的強度は曲げ強度が132.9kg
/cm2、剥離強度が4.3kg/cm2と良好であった。また、
熱圧成形時の圧締不足、熱圧成形後の厚みもどりもなく
外観も良好であった。Example 5 A particle board was produced in the same manner as in Example 1 except that 10 parts by weight of the synthetic resin foam particles D obtained in Reference Example 4 were used. The density of the obtained particle board is 0.4
3g / cm3, mechanical strength is flexural strength 132.9kg
/ cm2, and the peel strength was as good as 4.3 kg / cm2. Also,
The appearance was good with no insufficient tightening during hot-press forming and no thickness after hot-press forming.
【0029】[0029]
【効果】本発明によれば密度0.5g/cm3 以下の軽量パ
ーティクルボードが容易に、安定して安価に製造でき
る。また、機械的強度及び表面の平滑性も良好で、通常
のパーティクルボードと同等の化粧紙、化粧板等の貼着
や塗装も可能である。更に、得られた軽量パーティクル
ボードを従来のパーティクルボードの代替品として使用
した場合、家具の梱包使用の簡略化、梱包材料費や運賃
等のコストダウンがはかれる。また、廃棄された発泡ポ
リスチレン等も熱処理、加圧処理を施して使用すること
もできるので、世界的環境問題にも少なからず貢献でき
るものである。[Effect] According to the present invention, a lightweight particle board having a density of 0.5 g / cm 3 or less can be easily, stably and inexpensively manufactured. Further, it has good mechanical strength and smoothness on the surface, and it can be attached or coated with a decorative paper, a decorative plate or the like, which is the same as an ordinary particle board. Furthermore, when the obtained lightweight particle board is used as a substitute for the conventional particle board, the use of furniture for packing can be simplified, and costs such as packing materials and freight can be reduced. Further, since discarded expanded polystyrene and the like can also be used after being subjected to heat treatment and pressure treatment, it can contribute to the global environmental problem to some extent.
【図1】本発明の軽量パーティクルボードの中層を説明
する拡大断面図である。FIG. 1 is an enlarged cross-sectional view illustrating an intermediate layer of the lightweight particle board of the present invention.
1 軽量パーティクルボード 2 軽量パーティクルボードの表層部分 3 軽量パーティクルボードの中層部分 4 合成樹脂発泡粒 5 中層部の木質チップ 6 空隙 1 Lightweight particle board 2 Surface layer of light weight particle board 3 Middle layer of light weight particle board 4 Foamed synthetic resin particles 5 Wood chips of middle layer 6 Void
Claims (3)
ップ100重量部及び見かけ比重が0.3以下、圧縮弾
性率が30kg/cm2以上の合成樹脂発泡粒5〜30重量部
からなることを特徴とする軽量パーティクルボード。1. The middle layer of three-layer particle board is composed of 100 parts by weight of wood chips and 5 to 30 parts by weight of synthetic resin foam particles having an apparent specific gravity of 0.3 or less and a compression elastic modulus of 30 kg / cm 2 or more. And lightweight particle board.
ことを特徴とする請求項1記載の軽量パーティクルボー
ド。2. The lightweight particle board according to claim 1, wherein wood chips having a specific gravity of less than 0.5 are used.
ることを特徴とする請求項1記載の軽量パーティクルボ
ード。3. The lightweight particle board according to claim 1, wherein the synthetic resin foam particles are made of polystyrene.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21566692A JPH0631708A (en) | 1992-07-20 | 1992-07-20 | Light-weight particle board |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21566692A JPH0631708A (en) | 1992-07-20 | 1992-07-20 | Light-weight particle board |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0631708A true JPH0631708A (en) | 1994-02-08 |
Family
ID=16676164
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP21566692A Pending JPH0631708A (en) | 1992-07-20 | 1992-07-20 | Light-weight particle board |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0631708A (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH07133663A (en) * | 1993-11-10 | 1995-05-23 | Rinyachiyou Shinrin Sogo Kenkyusho | Vibration absorbable woody board |
JP2001293706A (en) * | 2000-04-14 | 2001-10-23 | Matsushita Electric Works Ltd | Particle board |
WO2007116676A1 (en) | 2006-03-31 | 2007-10-18 | Kuraray Kuraflex Co., Ltd. | Molded object having nonwoven fibrous structure |
EP1914052A1 (en) * | 2006-10-19 | 2008-04-23 | Basf Se | Lightweight wooden material |
US7781052B2 (en) * | 2004-05-31 | 2010-08-24 | Sumitomo Forestry Co., Ltd. | Method for making particle board |
US20100311854A1 (en) * | 2007-10-19 | 2010-12-09 | Bernard Thiers | Board, methods for manufacturing boards, and panel which comprises such board material |
US8187709B2 (en) | 2007-09-19 | 2012-05-29 | Basf Se | Light wood-based materials having good mechanical properties and low formaldehyde emission |
JP2012518563A (en) * | 2009-02-26 | 2012-08-16 | クロノテック・アーゲー | Induction wood board and method for producing induction wood board |
JP2015506284A (en) * | 2011-12-23 | 2015-03-02 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | Lignocellulosic material having lignocellulosic fibers in the outer layer and expanded plastic particles present in the core, and methods and uses thereof |
CN104786342A (en) * | 2015-04-24 | 2015-07-22 | 东北林业大学 | Wood composite board with low-density sandwich-type structure and preparation method thereof |
WO2017072220A1 (en) * | 2015-10-27 | 2017-05-04 | Synbra Technology B.V. | A process for preparing a wood chip board |
-
1992
- 1992-07-20 JP JP21566692A patent/JPH0631708A/en active Pending
Cited By (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH07133663A (en) * | 1993-11-10 | 1995-05-23 | Rinyachiyou Shinrin Sogo Kenkyusho | Vibration absorbable woody board |
JP2001293706A (en) * | 2000-04-14 | 2001-10-23 | Matsushita Electric Works Ltd | Particle board |
US7781052B2 (en) * | 2004-05-31 | 2010-08-24 | Sumitomo Forestry Co., Ltd. | Method for making particle board |
WO2007116676A1 (en) | 2006-03-31 | 2007-10-18 | Kuraray Kuraflex Co., Ltd. | Molded object having nonwoven fibrous structure |
US9758925B2 (en) | 2006-03-31 | 2017-09-12 | Kuraray Co., Ltd. | Molded object having nonwoven fibrous structure |
WO2008046890A3 (en) * | 2006-10-19 | 2008-06-12 | Basf Se | Light wood-based materials |
EP2319670A1 (en) * | 2006-10-19 | 2011-05-11 | Basf Se | Lightweight wooden material |
WO2008046890A2 (en) * | 2006-10-19 | 2008-04-24 | Basf Se | Light wood-based materials |
WO2008046892A3 (en) * | 2006-10-19 | 2008-08-21 | Basf Se | Light wood-based materials |
DE202006020503U1 (en) | 2006-10-19 | 2008-10-09 | Basf Se | Light wood materials |
JP2010506757A (en) * | 2006-10-19 | 2010-03-04 | ビーエーエスエフ ソシエタス・ヨーロピア | Lightweight wood material |
JP2010506758A (en) * | 2006-10-19 | 2010-03-04 | ビーエーエスエフ ソシエタス・ヨーロピア | Light weight wood material with good mechanical properties |
EA013665B1 (en) * | 2006-10-19 | 2010-06-30 | Басф Се | Light wood-based materials |
EA013666B1 (en) * | 2006-10-19 | 2010-06-30 | Басф Се | Light wood-based material |
WO2008046891A1 (en) * | 2006-10-19 | 2008-04-24 | Basf Se | Light wood materials with good mechanical characteristics |
EP1914052A1 (en) * | 2006-10-19 | 2008-04-23 | Basf Se | Lightweight wooden material |
WO2008046892A2 (en) * | 2006-10-19 | 2008-04-24 | Basf Se | Light wood-based materials |
US9089991B2 (en) | 2006-10-19 | 2015-07-28 | Basf Se | Light wood-based materials |
US8304069B2 (en) | 2006-10-19 | 2012-11-06 | Basf Se | Light wood-based materials |
US8187709B2 (en) | 2007-09-19 | 2012-05-29 | Basf Se | Light wood-based materials having good mechanical properties and low formaldehyde emission |
US20100311854A1 (en) * | 2007-10-19 | 2010-12-09 | Bernard Thiers | Board, methods for manufacturing boards, and panel which comprises such board material |
US10118311B2 (en) * | 2007-10-19 | 2018-11-06 | Flooring Industries Limited, Sarl | Board, methods for manufacturing boards, and panel which comprises such board material |
US11292151B2 (en) | 2007-10-19 | 2022-04-05 | Flooring Industries Limited, Sarl | Methods for manufacturing boards, and profiled element for manufacturing boards |
JP2012518563A (en) * | 2009-02-26 | 2012-08-16 | クロノテック・アーゲー | Induction wood board and method for producing induction wood board |
JP2015506284A (en) * | 2011-12-23 | 2015-03-02 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | Lignocellulosic material having lignocellulosic fibers in the outer layer and expanded plastic particles present in the core, and methods and uses thereof |
CN104786342A (en) * | 2015-04-24 | 2015-07-22 | 东北林业大学 | Wood composite board with low-density sandwich-type structure and preparation method thereof |
WO2017072220A1 (en) * | 2015-10-27 | 2017-05-04 | Synbra Technology B.V. | A process for preparing a wood chip board |
NL2015667B1 (en) * | 2015-10-27 | 2017-05-29 | Synbra Tech B V | A process for preparing a wood chip board. |
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