JP2006225931A - Flame-proofing panel - Google Patents

Flame-proofing panel Download PDF

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JP2006225931A
JP2006225931A JP2005039681A JP2005039681A JP2006225931A JP 2006225931 A JP2006225931 A JP 2006225931A JP 2005039681 A JP2005039681 A JP 2005039681A JP 2005039681 A JP2005039681 A JP 2005039681A JP 2006225931 A JP2006225931 A JP 2006225931A
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sheet
core material
flame
foaming
foam
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JP4921716B2 (en
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Fumitake Nagamori
文剛 永森
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Sekisui Chemical Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a flame-proofing panel excellent in light weight and capable of achieving both a satisfactory flame-proofing property and a satisfactory property to be pinned up. <P>SOLUTION: In a core material 3, face materials for suppressing a foaming force in in-plane directions, which occurs when foaming sheet raw fabric of a polyolefin-based resin foam is heated and foamed, are layered on both surfaces of a polyolefin-based resin foam in which individual bubbles are oriented in thickness directions. Metal sheets 21 and 22 (preferably aluminum sheets) and/or flame-proofing face materials 1 are layered on at least one surface of the core material 3. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

本発明は、防炎パネルに関し、より詳細には、軽量で且つピンナップ性と防炎性を兼ね備えた防炎パネルに関する。   The present invention relates to a flameproof panel, and more particularly, to a lightweight flameproof panel having both pinup and flameproof properties.

従来、展示会などに使用される間仕切り用パネルや展示パネルは一般的に可燃性の木質系及びスチレンフォームなどの発泡樹脂等の可燃性パネルを芯材としたものが多く使用されてきた。近年、防火上の問題から芯材自体に不燃、難燃処理を施したものや表層の化粧面材に同じく不燃、難燃処理を施したものを芯材に積層したものが使用されつつある。   2. Description of the Related Art Conventionally, partition panels and display panels used in exhibitions and the like have been used in many cases with flammable wood and flammable panels such as styrene foam as core materials. In recent years, due to fire prevention problems, those obtained by subjecting the core material itself to incombustibility and flame retardancy, and those obtained by laminating the surface layer decorative face material that has been subjected to the same incombustibility and flame retardancy treatment to the core material are being used.

しかし、木質系のパネルを芯材に用いた場合、重量が大きく施工上の障害が発生しやすくなる。また、発泡樹脂系の素材の場合には、所謂ピンナップ性が阻害され、展示物をピンにてパネルに固定することに支障が出ることがある。   However, when a wood-based panel is used as a core material, the weight is large, and it becomes easy to cause an obstacle in construction. In the case of a foamed resin material, the so-called pin-up property is hindered, and it may be difficult to fix the exhibit to the panel with pins.

上記の様な課題を解決する手段として、例えば特許文献1には、ハニカム材や合成樹脂発泡体等の芯材の両面に、繊維板、合板及び木材等の可燃性で、かつピンナップ性に優れた基材を接合し、各々の基材の表面側にケイ酸カルシウム紙を難燃剤を混入させた接着剤により接着するとともに、各々のケイ酸カルシウム紙の表面側に防炎加工されたシート状装飾材を難燃剤を混入させた接着剤により接着したことを特徴とする防炎パネルなどが開示されている。   As means for solving the above-mentioned problems, for example, Patent Document 1 discloses that both sides of a core material such as a honeycomb material and a synthetic resin foam are flammable, such as fiberboard, plywood and wood, and have excellent pinup properties. The base material is bonded to each other, and the surface of each base material is bonded with calcium silicate paper with an adhesive mixed with a flame retardant. A flameproof panel characterized by adhering a decorative material with an adhesive mixed with a flame retardant is disclosed.

しかし上記の場合、ハニカム材や合成樹脂発泡体等の比重の軽い芯材に対しピンナップ性を保持する為に木質系パネルを積層する構成であるために、重量が大きくなるなどの施工・組立て上の問題とともに、製造上のコストアップが懸念される。   However, in the above case, the construction is such that the weight increases because the wood panel is laminated in order to maintain pinup properties on the core material with a low specific gravity such as honeycomb material or synthetic resin foam. In addition to this problem, there is a concern about an increase in manufacturing costs.

また、樹脂発泡体を芯材として、防炎処理を施したり防炎効果が期待できるシートを積層させることで、構成全体としての防炎機能を付与できたとしても、一般的に5倍以下の発泡倍率の場合は、表面層が固くピンを刺す際に支障が出やすくなる。反面、樹脂発泡体が5倍以上の発泡倍率の場合は、ピンを刺すことはできるが、ピンの固定が不安定になりやすく、展示用パネル等の掲示物を固定するのに有効なピンナップ性が阻害される傾向にある。   Moreover, even if the flameproofing function as a whole structure can be provided by laminating sheets that can be subjected to a flameproofing treatment or expected to have a flameproofing effect using the resin foam as a core material, generally it is 5 times or less. In the case of the expansion ratio, the surface layer is hard, and it becomes easy to cause trouble when the pin is inserted. On the other hand, if the resin foam has a foaming ratio of 5 times or more, the pin can be stabbed, but pin fixing is likely to be unstable, and pin-up properties that are effective for fixing displays such as display panels. Tends to be inhibited.

特開平8−199705号公報JP-A-8-199705

本発明の目的は、上記の問題を解決し、軽量性に優れたポリオレフィン系硬質発泡体を用いつつも、良好なピンナップ性と防炎性を発揮し得る防炎パネルを提供することにある。   An object of the present invention is to solve the above problems and provide a flameproof panel that can exhibit good pinup properties and flameproofness while using a polyolefin-based rigid foam excellent in lightness.

請求項1記載の防炎パネルは、個々の気泡が厚み方向に配向しているポリオレフィン系樹脂発泡体の両面に、前記ポリオレフィン系樹脂発泡体の発泡性シート原反を加熱発泡する際に生じる面内方向の発泡力を抑制する為の面材が積層されてなる芯材の少なくとも片面に、金属シート及び/又は防炎処理が施された面材が積層されてなることを特徴とする。   The flameproof panel according to claim 1 is a surface generated when the foamable sheet raw material of the polyolefin resin foam is heated and foamed on both surfaces of the polyolefin resin foam in which individual bubbles are oriented in the thickness direction. A metal sheet and / or a face material that has been subjected to a flameproof treatment are laminated on at least one surface of a core material that is laminated with a face material for suppressing the foaming force in the inward direction.

請求項2記載の防炎パネルは、請求項1記載の防炎パネルであって、金属シートがアルミニウムシートであることを特徴とする。   The flameproof panel according to claim 2 is the flameproof panel according to claim 1, wherein the metal sheet is an aluminum sheet.

以下、本発明を詳細に説明する。   Hereinafter, the present invention will be described in detail.

本発明における芯材は、個々の気泡が厚み方向に配向している、ポリオレフィン系樹脂発泡体の両面に、前記ポリオレフィン系樹脂発泡体の発泡性原反シートを加熱発泡する際に生じる面内方向の発泡力を抑制する為の面材が積層されてなるものである。   The core material in the present invention is an in-plane direction generated when the foamable raw sheet of the polyolefin resin foam is heated and foamed on both surfaces of the polyolefin resin foam, in which individual bubbles are oriented in the thickness direction. The face material for suppressing the foaming force is laminated.

上記芯材の製造方法としては、特に限定されないが、例えば、ポリオレフィン系樹脂およびジオキシム化合物、ビスマレイミド、ジビニルベンゼン、アリル系多官能モノマー、(メタ)アクリル系多官能モノマーおよびキノン化合物から選択される少なくとも1種類の変性用モノマーと溶融混和して得られる変性ポリオレフィン100重量部に対して、アゾジカルボンアミド等の熱分解型化学発泡剤を2〜20重量部を分散させ、これを一旦シート状に成形して発泡性シート原反とした後、得られた発泡性シート原反の両面に面材を融着させ、原反を熱分解型化学発泡剤の分解温度以上に加熱して、該面材によって面内方向に生じる発泡力を抑制しつつこれを厚み方向にのみ発泡させる方法が挙げられる。   The method for producing the core material is not particularly limited. For example, the core material is selected from polyolefin resins and dioxime compounds, bismaleimide, divinylbenzene, allyl polyfunctional monomers, (meth) acrylic polyfunctional monomers, and quinone compounds. 2 to 20 parts by weight of a thermal decomposable chemical foaming agent such as azodicarbonamide is dispersed in 100 parts by weight of a modified polyolefin obtained by melt-mixing with at least one type of modifying monomer. After forming the foamable sheet raw fabric by molding, the surface material is fused to both sides of the obtained foamable sheet raw fabric, and the raw fabric is heated to a temperature equal to or higher than the decomposition temperature of the thermal decomposition type chemical foaming agent. There is a method of foaming only in the thickness direction while suppressing foaming force generated in the in-plane direction by the material.

ポリオレフィン系樹脂を上記のように変性させることで、成形された発泡性シート原反は架橋度が低いにも拘らず、これを常圧で発泡させ、さらに発泡方向に異方性を持たせることが可能となる。   By modifying the polyolefin resin as described above, it is possible to foam the foamed sheet at normal pressure and have anisotropy in the foaming direction even though the molded foam sheet has a low degree of crosslinking. Is possible.

ここで架橋度が低いとはゲル分率が25%以下であることをいう。一般的にゲル分率の測定は、サンプルの初期重量と、サンプルを120℃の熱キシレン中で24時間で溶解させたもののゲル分を乾燥させたものとの重量比で表現する。   Here, the low degree of crosslinking means that the gel fraction is 25% or less. In general, the measurement of the gel fraction is expressed by a weight ratio between the initial weight of the sample and the sample obtained by dissolving the sample in hot xylene at 120 ° C. for 24 hours and drying the gel.

本発明におけるポリオレフィン系樹脂とは、オレフィン性モノマーの(共)重合体であり、特に限定されるものではないが、例えば、低密度ポリエチレン、高密度ポリエチレン、直鎖状低密度ポリエチレン等のポリエチレン、ホモタイプポリプロピレン、ランダム
タイプポリプロピレン、ブロックタイプポリプロピレン等のポリプロピレン、ポリブテン、エチレン−プロピレン共重合体、エチレン−プロピレン−ジエン三元共重合体、エチレン−ブテン共重合体、エチレン−酢酸ビニル共重合体、エチレン−アクリル酸エステル共重合体等のエチレンを主成分とする共重合体などから選ばれる1種もしくは2種以上の単体および混合物を意味する。尚、ここで言う「(共)重合体」とは「重合体」または「共重合体」を意味する。
The polyolefin-based resin in the present invention is a (co) polymer of an olefinic monomer and is not particularly limited. For example, polyethylene such as low density polyethylene, high density polyethylene, and linear low density polyethylene, Homotype polypropylene, random type polypropylene, block type polypropylene and other polypropylene, polybutene, ethylene-propylene copolymer, ethylene-propylene-diene terpolymer, ethylene-butene copolymer, ethylene-vinyl acetate copolymer, It means one or more simple substances and mixtures selected from ethylene-based copolymers such as ethylene-acrylic acid ester copolymers. The “(co) polymer” mentioned here means “polymer” or “copolymer”.

上記ポリオレフィン系樹脂には30重量%を下回る範囲で、他の樹脂、例えば、ポリスチレン、スチレン系エラストマーなどがブレンドされていても良い。しかし30重量%を上回るとポリオレフィンの特徴(軽量、耐薬品性、柔軟性、弾性等)が発揮できないばかりか、発泡に必要な溶融粘度を確保することが困難となる場合がある。本発明でのポリオレフィン系樹脂としては、特にポリエチレンやポリプロピレンの1種もしくは2種以上が好適に用いられる。   The polyolefin-based resin may be blended with other resins such as polystyrene and styrene-based elastomer within a range of less than 30% by weight. However, if it exceeds 30% by weight, not only the characteristics of the polyolefin (light weight, chemical resistance, flexibility, elasticity, etc.) cannot be exhibited, but it may be difficult to ensure the melt viscosity necessary for foaming. As the polyolefin-based resin in the present invention, one or more of polyethylene and polypropylene are particularly preferably used.

熱分解型化学発泡剤は、加熱により分解ガスを発生するもので有れば特に限定されるものではなく、次ぎのものが例示される。アゾジカルボンアミド、ベンゼンスルホニルヒドラジド、ジニトロソペンタメチレンテトラミン、トルエンスルホニルヒドラジド、4,4−オキシビス(ベンゼンスルホニルヒドラジド)。これらは単独であるいは2種以上が混合されて用いられる。その中でもアゾジカルボンアミドが好適に用いられる。   The pyrolytic chemical foaming agent is not particularly limited as long as it generates a decomposition gas by heating, and the following are exemplified. Azodicarbonamide, benzenesulfonyl hydrazide, dinitrosopentamethylenetetramine, toluenesulfonyl hydrazide, 4,4-oxybis (benzenesulfonyl hydrazide). These may be used alone or in admixture of two or more. Of these, azodicarbonamide is preferably used.

発泡性シート原反の賦形方法としては、押出成形の他、プレス成形、ブロー成形、カレンダリング成形、射出成形など、プラスチックの成形加工で一般的に行われる方法が適用可能である。しかしスクリュー押出機より吐出する発泡性樹脂組成物を直接賦形する方法が、生産性の観点から好ましい。この場合は、一定寸法幅の連続発泡性シートを得ることができる。   As a method for shaping the foamable sheet material, methods generally used in plastic molding, such as press molding, blow molding, calendering, injection molding, etc., can be applied in addition to extrusion molding. However, the method of directly shaping the foamable resin composition discharged from the screw extruder is preferred from the viewpoint of productivity. In this case, a continuous foam sheet having a constant width can be obtained.

発泡性シート原反の両面に面材を積層する方法は特に限定されるものではないが、例えば、(イ)一旦冷却固化した発泡性シートに面材を加熱しながら貼付する方法、(ロ)発泡性シートを溶融状態になるまで加熱しておき、これを面材に熱融着する方法、(ハ)発泡性シートに面材を接着剤で貼り合わせる方法などが挙げられる。   The method of laminating the face material on both surfaces of the original foam sheet is not particularly limited. For example, (a) a method of applying the face material to the foam sheet once cooled and solidified while heating, (b) Examples thereof include a method of heating the foamable sheet until it is in a molten state and thermally fusing it to the face material, and (c) a method of attaching the face material to the foamable sheet with an adhesive.

発泡性複合シートすなわち芯材の厚み精度を確保するには方法(イ)または(ハ)が最も好ましい。方法(ロ)の熱融着法としては、例えば、Tダイから押し出された直後の溶融状態の発泡性シート原反の少なくとも片面に面材を軽く積層した状態で、これらを対向状の冷却ロール間を通過させ、ロールの押圧力で両者を一体化する方法が好ましい。なお、上記のように発泡性シート原反と面材を積層して一体化するとは、原反と面材を両者の界面において剥離しようとした場合に、高い割合で材料破壊が生じる程度に両者が固着されている状態を意味するものとする。   In order to ensure the thickness accuracy of the foamable composite sheet, that is, the core material, the method (a) or (c) is most preferable. Examples of the method (b) of heat fusion include, for example, in a state where a face material is lightly laminated on at least one surface of a molten foam sheet immediately after being extruded from a T-die, and these are opposed cooling rolls. A method in which the two are passed through and integrated with the pressing force of the roll is preferable. In addition, when the original sheet and the face material are laminated and integrated as described above, when both the raw material and the face material are peeled at the interface between the two, both materials are broken to such a degree that material destruction occurs at a high rate. Means a state in which is fixed.

ポリオレフィン系樹脂発泡性シート原反の発泡方向を規制するのに使用される面材は、厚さ1mm未満のシート材である。その具体例は以下のものがある。   The face material used to regulate the foaming direction of the polyolefin resin foam sheet is a sheet material having a thickness of less than 1 mm. Specific examples are as follows.

1)ガラスクロス
ガラスクロスの代表例は、ガラス繊維を抄造して得られるサーフェイスマット、ガラスロービングが織られて作成されるものである。サーフェイスマットは、ガラス短繊維同士を結着するためのバインダーを含んでいてもよい。該バインダーは、面材の引張強度が上記範囲を満たすものであれば特に限定されず、例えば、ポリビニルアルコール、飽和ポリエステル、アクリル系樹脂などの熱可塑性樹脂や、エポキシ樹脂、不飽和ポリエステルなどの熱硬化性樹脂が挙げられる。
1) Glass cloth A typical example of a glass cloth is one produced by weaving a surface mat or glass roving obtained by making glass fibers. The surface mat may contain a binder for binding the short glass fibers. The binder is not particularly limited as long as the tensile strength of the face material satisfies the above range. For example, thermoplastic resins such as polyvinyl alcohol, saturated polyester, and acrylic resin, and heat such as epoxy resin and unsaturated polyester are used. A curable resin is mentioned.

2)カーボンマット
3)織布、不織布、寒冷紗、ニードルパンチ
これらを構成する有機繊維としてはポリエステル繊維、アクリル繊維、ナイロン繊維、炭素繊維、アラミド繊維等が挙げられる。また、綿やケナフ等の天然繊維等がある。
2) Carbon mat 3) Woven fabric, non-woven fabric, cold water, needle punch Examples of organic fibers constituting these include polyester fiber, acrylic fiber, nylon fiber, carbon fiber, and aramid fiber. There are also natural fibers such as cotton and kenaf.

4)紙類
紙類としては、パルプ系(セルロース含有量90%以上)等がある。
4) Papers Examples of papers include pulp (cellulose content of 90% or more).

面材の目付重量は好ましくは10〜300g/mmである。目付重量が10g/mm未満であると、ピンナップ性が得られ難くなることがあり、300g/mmを超えると、面材の柔軟性が損なわれ、これを芯材に連続的に貼り付けることが困難となり、また面材を介して発泡性シートを加熱することが難しくなるため面材と発泡性シートが均一に融着せず剥離等により気泡構造が不均一となる。 The basis weight of the face material is preferably 10 to 300 g / mm 2 . If the weight per unit area is less than 10 g / mm 2 , pinup properties may be difficult to obtain. If it exceeds 300 g / mm 2 , the flexibility of the face material is impaired, and this is continuously pasted to the core material. In addition, since it becomes difficult to heat the foamable sheet through the face material, the face material and the foamable sheet are not fused uniformly, and the cell structure becomes non-uniform due to peeling or the like.

発泡性シート原反の発泡は、通常、熱分解型化学発泡剤の分解温度以上、熱可塑性樹脂の熱分解温度以下の温度範囲で行われる。特に連続式発泡装置としては、加熱炉の出口側で発泡体を引き取りながら発泡させる引き取り式発泡器の他、ベルト式発泡器、縦型または横型発泡炉、熱風恒温槽など、あるいは熱浴中で発泡を行うオイルバス、メタルバス、ソルトバスなどが使用される。   Foaming of the original foamable sheet is usually performed in a temperature range not lower than the decomposition temperature of the pyrolytic chemical foaming agent and not higher than the thermal decomposition temperature of the thermoplastic resin. In particular, as a continuous foaming device, in addition to a take-off foamer that foams while taking out the foam on the outlet side of the heating furnace, a belt-type foamer, a vertical or horizontal foaming furnace, a hot air thermostat, etc., or in a hot bath Foaming oil baths, metal baths, salt baths, etc. are used.

上記方法で製造された発泡体は、気泡径の長軸が厚み方向に配列しており、圧縮強度に優れた物性を示す。   The foam produced by the above-described method has the long axis of the cell diameter arranged in the thickness direction and exhibits physical properties excellent in compressive strength.

上記発泡体の発泡倍率としては、特に限定されないが、軽量性とピンアップ性のバランスの点で、5〜30倍であることが好ましい。   Although it does not specifically limit as an expansion ratio of the said foam, It is preferable that it is 5 to 30 times from the point of the balance of lightweight property and pinup property.

本発明においては、上記芯材が用いられることで、ピンナップ性に優れたものとなる。ここでピンナップ性とは、ピンをパネル類に刺し固定する機能を指す。一般的に発泡スチロールやウレタン系の高倍率発泡体ではピンナップ性が劣る傾向がある。インシュレーションボードやコルク、バルサ材など繊維を含む素材は、通常良好なピンナップ性が得られる、これは、指したピンに繊維層が絡むことで固定保持機能が発生することに起因していると考えられる。樹脂プレートや無機系ボードでは堅すぎて通常ピンを刺すことは困難である。   In this invention, it becomes what was excellent in pinup property by using the said core material. Here, the pinup property refers to a function of inserting and fixing a pin in a panel. Generally, the pinup property tends to be inferior in the foamed polystyrene or urethane-based high-magnification foam. Insulation boards, corks, balsa materials, and other materials that contain fibers usually have good pinup properties. This is due to the fact that the fiber layer is entangled with the pin that is pointed to cause a fixed holding function. Conceivable. Resin plates and inorganic boards are too hard to puncture normally.

本発明においては、上記のような気泡が厚み方向に配向している、ポリオレフィン系樹脂発泡体の両面に、前記ポリオレフィン系樹脂発泡体の発泡性シート原反を加熱発泡する際に生じる面内方向の発泡力を抑制する為の面材が積層されてなる芯材を用いることで、表面に積層された面材によりピンの固定保持性を向上する効果、及び、ポリオレフィン系樹脂発泡体の面材に接する部分に密度の高いスキン層が形成されることによりピンの固定保持性を向上する効果などが発揮されるためと推定される。   In the present invention, the above-mentioned air bubbles are oriented in the thickness direction, and the in-plane direction generated when the foamable sheet raw fabric of the polyolefin resin foam is heated and foamed on both surfaces of the polyolefin resin foam. By using a core material in which a face material for suppressing the foaming force of the material is laminated, the effect of improving pin fixing and holding performance by the face material laminated on the surface, and the face material of the polyolefin resin foam It is presumed that the effect of improving the pin fixing and retaining property is exhibited by forming a skin layer having a high density in a portion in contact with the pin.

従って、ポリオレフィン系樹脂発泡体の発泡倍率を高くしても、良好なピンナップ性が得られるので、芯材の比重を合板の1/3以下にすることも可能である。   Therefore, even if the foaming ratio of the polyolefin resin foam is increased, good pinup properties can be obtained, so that the specific gravity of the core material can be 1/3 or less of the plywood.

本発明の防炎パネルは、上記芯材の少なくとも片面に、金属シート及び/又は防炎処理が施された面材が積層されてなるものである。   The flameproof panel of the present invention is formed by laminating a metal sheet and / or a flameproofed surface material on at least one surface of the core material.

上記金属シートとしては、特に限定されないが、アルミニウムシートが軽量性と防炎性のバランスに優れている点で好ましい。
上記アルミニウムシートを単独で用いる場合にはその厚みは5〜80μmが好ましい。
厚みが5μm未満の場合には、防炎性が不十分となり、50μmを超えるとピンアップ性及び軽量性が損なわれるからである。
Although it does not specifically limit as said metal sheet, An aluminum sheet is preferable at the point which is excellent in the balance of lightweight and flameproofness.
When the aluminum sheet is used alone, the thickness is preferably 5 to 80 μm.
This is because when the thickness is less than 5 μm, the flameproofness is insufficient, and when it exceeds 50 μm, the pin-up property and the lightness are impaired.

上記防炎処理が施された面材としては、特に限定されず、例えば、水酸化アルミニウム及びガラス繊維等の無機物を配合した不燃紙などが挙げられが、中でも、水酸化アルミニウム及びガラス繊維等の無機物を配合した不燃紙が好ましい。これは、火炎が不燃紙に達し、燃焼開始温度に達すると配合されている水酸化アルミニウムと酸素が反応し吸熱反応を開始し、その際、酸化反応により水が析出され自己消化作用が発生する。従って、不燃紙自体の延焼をとどめる効果が発生するとともに、表層の延焼が食い止められることで、雰囲気温度の上昇を抑えかつ不燃紙から発生した水分により芯材の延焼も最低限にとどめる効果が期待されるためである。
上記面材の目付重量は好ましくは30g/m以上、さらに好ましくは50〜300g/mである。目付重量が少なすぎると防炎性が不十分となり、多すぎると芯材へ積層しづらくなるからである。
The face material subjected to the above flameproofing treatment is not particularly limited, and examples thereof include non-combustible paper containing an inorganic substance such as aluminum hydroxide and glass fiber. Among them, aluminum hydroxide and glass fiber are particularly preferable. Non-combustible paper containing an inorganic substance is preferred. This is because when the flame reaches the non-combustible paper and the combustion start temperature is reached, the compounded aluminum hydroxide reacts with oxygen to start an endothermic reaction. At this time, water is precipitated by the oxidation reaction and self-digestion occurs. . Therefore, the effect of suppressing the spread of the non-combustible paper itself is generated, and by suppressing the spread of the surface layer, it is expected to suppress the increase in the ambient temperature and minimize the spread of the core material due to moisture generated from the non-combustible paper. Because it is done.
Weight per unit area of the surface material is preferably 30 g / m 2 or more, more preferably from 50 to 300 g / m 2. This is because if the weight per unit area is too small, the flameproofness becomes insufficient, and if it is too large, it is difficult to laminate the core material.

上記において、防炎性が施された面材と芯材との間に金属シートを介在させた場合には、芯材表面への直接的な火炎が芯材へ接することを食いとどめる他に、燃焼を発生させる酸素の供給を遮断する効果が期待され、この場合には更に防炎効果が向上する点で好ましい。   In the above, when a metal sheet is interposed between the face material and the core material subjected to flameproofness, in addition to stopping the direct flame to the core material surface from contacting the core material, The effect of blocking the supply of oxygen that generates combustion is expected, and in this case, it is preferable in that the flameproofing effect is further improved.

上記金属シート及び/又は防炎処理が施された面材の積層構成としては特に限定されず、単層でもよいし複層であっても良い、また、各々が交互に積層されたものであってもよい。   The laminated structure of the metal sheet and / or the face material subjected to the flameproofing treatment is not particularly limited, and may be a single layer or multiple layers, and each layer is alternately laminated. May be.

本発明の防炎パネルは、個々の気泡が厚み方向に配向している、ポリオレフィン系樹脂発泡体の両面に、前記ポリオレフィン系樹脂発泡体の発泡性シート原反を加熱発泡する際に生じる面内方向の発泡力を抑制する為の面材が積層されてなる芯材の少なくとも片面に、金属シート及び/又は防炎処理が施された面材が積層されてなることを特徴とするので、軽量で且つピンナップ性と防炎性を兼ね備えた防炎パネルを提供することができる。   The flameproof panel of the present invention has an in-plane generated when the foamed sheet raw fabric of the polyolefin resin foam is heated and foamed on both surfaces of the polyolefin resin foam in which individual bubbles are oriented in the thickness direction. Lightweight because it is characterized in that a metal sheet and / or a flameproofed surface material is laminated on at least one side of a core material in which a surface material for suppressing the foaming force in the direction is laminated In addition, it is possible to provide a flameproof panel having both pinup and flameproof properties.

金属シートがアルミニウムシートである場合には、軽量性と防炎性のバランスが向上し、上記効果は更に確実なものとなる。   In the case where the metal sheet is an aluminum sheet, the balance between lightness and flameproofness is improved, and the above effect is further ensured.

本発明を実施例によってより具体的に説明する。尚、本発明は下記実施例のみに限定されるものではない。   The present invention will be described more specifically with reference to examples. In addition, this invention is not limited only to the following Example.

(実施例1)
i)発泡性樹脂組成物の製造
(1)変性ポリオレフィン系樹脂の調製
変性用スクリュー押出機として、BT40(プラスチック工学研究所社製)同方向回転2軸スクリュー押出機を用いた。これはセルフワイピング2条スクリューを備え、そのL/Dは35、Dは39mmである。シリンダーバレルは押出機の上流から下流側へ第1〜4バレルからなり、ダイは3穴ストランドダイであり、揮発分を回収するため第4バレルに真空ベントが設置されている。
Example 1
i) Production of Expandable Resin Composition (1) Preparation of Modified Polyolefin Resin BT40 (manufactured by Plastic Engineering Laboratories) Co-rotating twin screw extruder was used as a modification screw extruder. This is equipped with a self-wiping double thread, L / D is 35 and D is 39 mm. The cylinder barrel is composed of first to fourth barrels from the upstream side to the downstream side of the extruder, the die is a three-hole strand die, and a vacuum vent is installed in the fourth barrel to collect volatile components.

操作条件は下記の通りである。   The operating conditions are as follows.

・シリンダーバレル設定温度:第1バレル;180℃
第2バレル;220℃
第3バレル;220℃
第4バレル;220℃
ダ イ;220℃
・スクリュー回転数:150rpm
・ Cylinder barrel set temperature: 1st barrel; 180 ℃
2nd barrel; 220 ° C
3rd barrel; 220 ° C
4th barrel; 220 ° C
Die: 220 ° C
・ Screw rotation speed: 150rpm

上記構成の変性用スクリュー押出機に、まず、ポリオレフィン系樹脂およびジオキシム化合物をその後端ホッパーから別々に投入し両者を溶融混和し、変性樹脂を得た。このとき、押出機内で発生した揮発分は真空ベントにより真空引きした。   First, a polyolefin resin and a dioxime compound were separately charged from the rear end hopper into the modification screw extruder having the above configuration, and both were melted and mixed to obtain a modified resin. At this time, the volatile matter generated in the extruder was evacuated by a vacuum vent.

ポリオレフィン系樹脂はポリプロピレンランダム共重合体(三菱化学製「EG8」、MI;0.8g/10分、密度;0.9g/cm)であり、その供給量は10kg/hとした。 The polyolefin resin was a polypropylene random copolymer (“EG8” manufactured by Mitsubishi Chemical Corporation, MI; 0.8 g / 10 min, density: 0.9 g / cm 3 ), and the supply amount was 10 kg / h.

変性用モノマーはp−キノンジオキシム(大内新興化学社製「バルノックGM−P」)であり、その供給量はポリオレフィン系樹脂100重量部に対して0.75重量部とした。   The modifying monomer was p-quinonedioxime (“Barunok GM-P” manufactured by Ouchi Shinsei Chemical Co., Ltd.), and the amount supplied was 0.75 parts by weight with respect to 100 parts by weight of the polyolefin resin.

ポリオレフィン系樹脂とジオキシム化合物の溶融混和によって得られた変性樹脂を、ストランドダイから吐出し、水冷し、ペレタイザーで切断して、変性樹脂のペレットを得た。   The modified resin obtained by melt-blending the polyolefin resin and the dioxime compound was discharged from a strand die, cooled with water, and cut with a pelletizer to obtain modified resin pellets.

(2)発泡性樹脂組成物の調製と複合シートの調製
発泡剤混練用スクリュー押出機はTEX−44型(日本製鋼所社製)同方向回転2軸スクリュー押出機であり、これはセルフワイピング2条スクリューを備え、そのL/Dは45.5、Dは47mmである。シリンダーバレルは押出機の上流から下流側へ第1〜12バレルからなり、成形ダイは出口幅500mm、出口隙間3.5mmのTダイである。
(2) Preparation of foamable resin composition and preparation of composite sheet The screw extruder for kneading the foaming agent is a TEX-44 type (manufactured by Nippon Steel Co., Ltd.) co-rotating twin screw extruder, which is self-wiping 2 A strip screw is provided, and the L / D is 45.5 and D is 47 mm. The cylinder barrel is composed of first to twelfth barrels from the upstream side to the downstream side of the extruder, and the forming die is a T die having an outlet width of 500 mm and an outlet gap of 3.5 mm.

温度設定区分は下記の通りである。   The temperature setting categories are as follows.

第1バレルは常時冷却
第1ゾーン;第2〜4バレル
第2ゾーン;第5〜8バレル
第3ゾーン;第9〜12バレル
第4ゾーン;ダイおよびアダプター部
The first barrel is always cooled
1st zone; 2-4 barrels
2nd zone; 5-8 barrels
3rd zone; 9th to 12th barrels
Zone 4; die and adapter section

発泡剤を供給するために第6バレルにサイドフィーダーが設置され、揮発分を回収するため第11バレルに真空ベントが設置されている。   A side feeder is installed in the sixth barrel for supplying the foaming agent, and a vacuum vent is installed in the eleventh barrel for recovering volatile components.

操作条件は下記の通りである。   The operating conditions are as follows.

・シリンダーバレル設定温度:第1バレル;150℃
第2バレル;170℃
第3バレル;180℃
第4バレル;160℃
・スクリュー回転数:40rpm
・ Cylinder barrel set temperature: 1st barrel; 150 ℃
Second barrel: 170 ° C
3rd barrel; 180 ° C
4th barrel; 160 ° C
-Screw rotation speed: 40rpm

上述のようにして得られた変性樹脂を反応用スクリュー押出機から発泡剤混練用スクリュー押出機に供給した。変性樹脂の供給量は20kg/hとした。また、同押出機にそのサイドフィーダーから発泡剤を供給し、分散させた。発泡剤はアゾジカルボンアミド(ADCA)であり、その供給量は1.2kg/hとした。   The modified resin obtained as described above was supplied from the reaction screw extruder to the blowing agent kneading screw extruder. The supply amount of the modified resin was 20 kg / h. Moreover, the foaming agent was supplied to the same extruder from the side feeder and dispersed. The blowing agent was azodicarbonamide (ADCA), and the supply amount was 1.2 kg / h.

こうして変性樹脂と発泡剤の混練によって得られた発泡性樹脂組成物を、Tダイから押し出し、3本冷却ロールに通す際に、発泡性樹脂組成物シートの表面、裏面の両面に、面材として、ポリエチレンテレフタレート製の不織布(東洋紡績社製、「スパンポンドエクーレ6301A」、目付重量30g/m、引張り強度:縦1.6kg/cm、横1.2kg/cm)を熱融着し、幅460mm、厚さ3.4mmのポリオレフィン系樹脂発泡性複合シートを得た。 When the foamable resin composition thus obtained by kneading the modified resin and the foaming agent is extruded from a T-die and passed through three cooling rolls, it is used as a face material on both the front and back surfaces of the foamable resin composition sheet. , A non-woven fabric made of polyethylene terephthalate (manufactured by Toyobo Co., Ltd., “Spunpond Ecule 6301A”, basis weight 30 g / m 2 , tensile strength: length 1.6 kg / cm, width 1.2 kg / cm), A polyolefin resin foamable composite sheet having a width of 460 mm and a thickness of 3.4 mm was obtained.

(3) 発泡
得られたポリオレフィン系樹脂発泡複合シートを加熱ゾーンを有する連続発泡機にて、230℃で約8分間加熱発泡させ、厚さ7mmの複合発泡体を得た。得られた複合発泡体を構成するポリオレフィン系樹脂発泡体は、気泡が厚み方向に配向し、発泡倍率は10倍であった。
(3) Foaming The obtained polyolefin-based resin foam composite sheet was heated and foamed at 230 ° C. for about 8 minutes using a continuous foaming machine having a heating zone to obtain a composite foam having a thickness of 7 mm. In the polyolefin resin foam constituting the obtained composite foam, the bubbles were oriented in the thickness direction, and the expansion ratio was 10 times.

得られた複合発泡体を芯材とし、図1に示すように、防炎処理が施された面材(以下、「不燃紙」ともいう)1、アルミニウムシート21(厚み7μm)、芯材3、アルミニウムシート22(厚み7μm)、普通紙4(目付重量60g/m)、がこの順に積層された防炎パネル5を作成した。尚、不燃紙1としては、水酸化アルミニウム及びガラス繊維等の無機物を配合した不燃紙(リンテック社製、「セラフォームW−135AF」、目付重量135g/m)を用いた。 The obtained composite foam is used as a core material, and as shown in FIG. 1, a face material (hereinafter also referred to as “non-combustible paper”) 1 subjected to a flameproof treatment, an aluminum sheet 21 (thickness 7 μm), and a core material 3 A flameproof panel 5 was prepared in which an aluminum sheet 22 (thickness 7 μm) and plain paper 4 (weight per unit area 60 g / m 2 ) were laminated in this order. As the non-combustible paper 1, non-combustible paper (“Cerafoam W-135AF”, weight per unit area 135 g / m 2 , manufactured by Lintec Co., Ltd.) containing inorganic substances such as aluminum hydroxide and glass fiber was used.

積層方法としては、不燃紙1とアルミニウムシート21とをポリエチレン系フィルムを介して熱ラミネート成形したものにロールコーターを用いてウレタン系反応型ホットメルト接着剤を塗布した後、芯材3の上面に加熱加圧して積層し、また、普通紙4とアルミニウムシート22とをポリエチレン系フィルムを介して熱ラミネート成形したものにロールコーターを用いてウレタン系反応型ホットメルト接着剤を塗布した後、芯材3の下面に加熱加圧して積層した。   As a laminating method, a non-flammable paper 1 and an aluminum sheet 21 are heat-laminated through a polyethylene film, a urethane coat type hot melt adhesive is applied using a roll coater, and then the upper surface of the core material 3 is applied. After laminating by heating and pressurizing, and applying a urethane-based reactive hot melt adhesive using a roll coater to a laminate of plain paper 4 and aluminum sheet 22 via a polyethylene film, a core material The lower surface of 3 was laminated by heating and pressing.

(実施例2)
不燃紙1として、水酸化アルミニウム及びガラス繊維等の無機物を配合した不燃紙(リンテック社製、「セラフォームHC−180A」、目付重量180g/m)を用いたこと以外は実施例1と同様にして防炎パネルを作成した。
(Example 2)
Example 1 is the same as Example 1 except that non-combustible paper (Made by Lintec, “Cerafoam HC-180A”, weight per unit area 180 g / m 2 ) containing inorganic substances such as aluminum hydroxide and glass fiber is used as non-combustible paper 1. A flameproof panel was made.

(実施例3)
不燃紙1として、水酸化アルミニウム及びガラス繊維等の無機物を配合した不燃紙(三善製紙社製、「サンウォール」、目付重量120g/m)を用いたこと以外は実施例1と同様にして防炎パネルを作成した。
(Example 3)
Except that non-combustible paper 1 (non-combustible paper made by Miyoshi Paper Co., Ltd., “Sunwall”, weight per unit area 120 g / m 2 ) was used as non-combustible paper 1 in the same manner as in Example 1. A fireproof panel was created.

(実施例4)
アルミニウムシートを用いなかったこと以外は実施例1と同様にして防炎パネルを作成した。
Example 4
A flameproof panel was prepared in the same manner as in Example 1 except that the aluminum sheet was not used.

(比較例1)
芯材3の両面に、不燃紙1(リンテック社製、「セラフォームW−135AF」、目付重量135g/m)を積層した防炎パネルを作成した。
(Comparative Example 1)
A flameproof panel in which non-combustible paper 1 (manufactured by Lintec Corporation, “Cerafoam W-135AF”, basis weight 135 g / m 2 ) was laminated on both surfaces of the core material 3 was prepared.

(比較例2)
発泡スチロール(厚み7mm、発泡倍率30倍)の両面に不燃紙(リンテック社製、「セラフォームW−135AF」、目付重量135g/m)が積層された防炎パネルを作成した。
(Comparative Example 2)
A flameproof panel in which non-combustible paper (manufactured by Lintec, “Cerafoam W-135AF”, weight per unit area 135 g / m 2 ) was laminated on both sides of polystyrene foam (thickness 7 mm, expansion ratio 30 times) was prepared.

(比較例3)
芯材3として発泡スチロール(厚み7mm、発泡倍率30倍)を用いたこと以外は実施例2と同様にして防炎パネルを作成した。
(Comparative Example 3)
A flameproof panel was prepared in the same manner as in Example 2 except that foamed polystyrene (thickness 7 mm, foaming ratio 30 times) was used as the core material 3.

上記実施例及び比較例について、防炎性能、ピンナップ性を評価した。尚、防炎性能は45°メッケルバーナー法(防炎協会における展示パネル用防炎試験に準拠)により評価した。評価結果は表1に示した。   About the said Example and comparative example, flameproof performance and pinup property were evaluated. The flameproof performance was evaluated by the 45 ° Meckel burner method (based on the flameproof test for display panels in the Flameproof Association). The evaluation results are shown in Table 1.

Figure 2006225931
Figure 2006225931

表1より明らかなように、本発明の防炎パネルは、高い防炎性能を有しつつも、軽量でピンナップ性に優れることが判明した。   As is clear from Table 1, the flameproof panel of the present invention was found to be lightweight and excellent in pinup properties while having high flameproof performance.

本発明の防炎パネルの一例を示す模式断面図である。It is a schematic cross section which shows an example of the flameproof panel of this invention.

符号の説明Explanation of symbols

1 防炎処理が施された面材(不燃紙)
21,22 金属シート(アルミニウムシート)
3 芯材
4 普通紙
5 防炎パネル
1 Face material (incombustible paper) that has been subjected to flameproofing
21, 22 Metal sheet (aluminum sheet)
3 Core material 4 Plain paper 5 Flameproof panel

Claims (2)

個々の気泡が厚み方向に配向しているポリオレフィン系樹脂発泡体の両面に、前記ポリオレフィン系樹脂発泡体の発泡性シート原反を加熱発泡する際に生じる面内方向の発泡力を抑制する為の面材が積層されてなる芯材の少なくとも片面に、金属シート及び/又は防炎処理が施された面材が積層されてなることを特徴とする防炎パネル。   In order to suppress the foaming force in the in-plane direction generated when the foamed sheet raw fabric of the polyolefin resin foam is heated and foamed on both surfaces of the polyolefin resin foam in which individual bubbles are oriented in the thickness direction A flameproof panel comprising a metal sheet and / or a flameproofed face material laminated on at least one surface of a core material obtained by laminating face materials. 金属シートがアルミニウムシートであることを特徴とする請求項1記載の防炎パネル。
The flameproof panel according to claim 1, wherein the metal sheet is an aluminum sheet.
JP2005039681A 2005-02-16 2005-02-16 Pinup flameproof panel Expired - Fee Related JP4921716B2 (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010053577A (en) * 2008-08-28 2010-03-11 Koyo Sangyo Co Ltd Flame retardant panel
JP2014102277A (en) * 2012-11-16 2014-06-05 Dow Chemical Company Flame-proof panel for exhibition

Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50140991U (en) * 1974-05-11 1975-11-20
JPS5444414Y2 (en) * 1974-05-27 1979-12-20
JPS58147440A (en) * 1982-02-26 1983-09-02 Asahi Chem Ind Co Ltd Foamed article of flame retardant thermoplastic resin
JPS6032989Y2 (en) * 1980-03-25 1985-10-02 株式会社ブリヂストン insulation board
JPH0611185Y2 (en) * 1988-05-21 1994-03-23 東洋ゴム工業株式会社 Flame retardant composite insulation board
JPH07214715A (en) * 1994-01-28 1995-08-15 Kanegafuchi Chem Ind Co Ltd Heat insulating panel
JPH08199704A (en) * 1995-01-30 1996-08-06 Okamura Corp Flameproof panel
JPH08199705A (en) * 1995-01-30 1996-08-06 Okamura Corp Flameproof panel
JPH08199709A (en) * 1995-01-30 1996-08-06 Okamura Corp Flameproof panel for partition
JPH11291425A (en) * 1997-10-29 1999-10-26 Sekisui Chem Co Ltd Manufacture of polyolefin resin foamable composite sheet and composite foam
JP2000218650A (en) * 1999-02-02 2000-08-08 Sekisui Chem Co Ltd Manufacture of flame-retardant composite foam
JP2001293829A (en) * 2000-02-10 2001-10-23 Sekisui Chem Co Ltd Polyolefinic resin composite laminate
JP2001310432A (en) * 2000-04-27 2001-11-06 Sekisui Chem Co Ltd Laminated composite foam
JP2002047795A (en) * 2000-08-03 2002-02-15 Sekisui Chem Co Ltd Plastic concrete form
JP2005156858A (en) * 2003-11-25 2005-06-16 Dow Kakoh Kk Flame-proof panel for exhibition
JP2005238573A (en) * 2004-02-25 2005-09-08 Sekisui Chem Co Ltd Polyolefinic resin composite foam

Patent Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50140991U (en) * 1974-05-11 1975-11-20
JPS5444414Y2 (en) * 1974-05-27 1979-12-20
JPS6032989Y2 (en) * 1980-03-25 1985-10-02 株式会社ブリヂストン insulation board
JPS58147440A (en) * 1982-02-26 1983-09-02 Asahi Chem Ind Co Ltd Foamed article of flame retardant thermoplastic resin
JPH0611185Y2 (en) * 1988-05-21 1994-03-23 東洋ゴム工業株式会社 Flame retardant composite insulation board
JPH07214715A (en) * 1994-01-28 1995-08-15 Kanegafuchi Chem Ind Co Ltd Heat insulating panel
JPH08199709A (en) * 1995-01-30 1996-08-06 Okamura Corp Flameproof panel for partition
JPH08199705A (en) * 1995-01-30 1996-08-06 Okamura Corp Flameproof panel
JPH08199704A (en) * 1995-01-30 1996-08-06 Okamura Corp Flameproof panel
JPH11291425A (en) * 1997-10-29 1999-10-26 Sekisui Chem Co Ltd Manufacture of polyolefin resin foamable composite sheet and composite foam
JP2000218650A (en) * 1999-02-02 2000-08-08 Sekisui Chem Co Ltd Manufacture of flame-retardant composite foam
JP2001293829A (en) * 2000-02-10 2001-10-23 Sekisui Chem Co Ltd Polyolefinic resin composite laminate
JP2001310432A (en) * 2000-04-27 2001-11-06 Sekisui Chem Co Ltd Laminated composite foam
JP2002047795A (en) * 2000-08-03 2002-02-15 Sekisui Chem Co Ltd Plastic concrete form
JP2005156858A (en) * 2003-11-25 2005-06-16 Dow Kakoh Kk Flame-proof panel for exhibition
JP2005238573A (en) * 2004-02-25 2005-09-08 Sekisui Chem Co Ltd Polyolefinic resin composite foam

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010053577A (en) * 2008-08-28 2010-03-11 Koyo Sangyo Co Ltd Flame retardant panel
JP2014102277A (en) * 2012-11-16 2014-06-05 Dow Chemical Company Flame-proof panel for exhibition

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