JPS5930543B2 - Composite panel with fire resistance - Google Patents

Composite panel with fire resistance

Info

Publication number
JPS5930543B2
JPS5930543B2 JP14439280A JP14439280A JPS5930543B2 JP S5930543 B2 JPS5930543 B2 JP S5930543B2 JP 14439280 A JP14439280 A JP 14439280A JP 14439280 A JP14439280 A JP 14439280A JP S5930543 B2 JPS5930543 B2 JP S5930543B2
Authority
JP
Japan
Prior art keywords
inorganic
composite panel
fire resistance
grains
foam
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP14439280A
Other languages
Japanese (ja)
Other versions
JPS5658851A (en
Inventor
尭 石川
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to JP14439280A priority Critical patent/JPS5930543B2/en
Publication of JPS5658851A publication Critical patent/JPS5658851A/en
Publication of JPS5930543B2 publication Critical patent/JPS5930543B2/en
Expired legal-status Critical Current

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  • Building Environments (AREA)

Description

【発明の詳細な説明】 本発明は高温にさらされる複合パネルにおいて、その表
面材の背面に耐火層を安定な状態で敷設することによつ
て可燃な合成樹脂発泡体層を高温から護りラる耐火性を
有する複合パネルに関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention protects a combustible synthetic resin foam layer from high temperatures by stably laying a fireproof layer on the back side of the surface material in a composite panel exposed to high temperatures. The present invention relates to a composite panel having fire resistance.

一般に合成樹脂発泡体、例えばポリウレタン樹脂の耐熱
性は通常における連続使用で100℃位といわれている
。しかし、このような低耐熱性にも拘らず、その優れた
物性、例えば軽量であること、自己接着性があり、かつ
加工性を有している等の理由から建材の芯材として汎用
されている。そして、この耐熱性を改善する方法が現在
まで多数公開実施されている、しかし、これら改善方法
に共通する欠点としては、1樹脂発泡倍率の低下を招く
こと。所謂、比重、嵩、形状の異なる異質物の添加、あ
るいは難燃剤の添加によつて樹脂単体のときの発泡倍率
より大幅に低下せしめられる。換言すれば、これら異質
物へのフォーム原料の付着量の増大と反応、発泡が僅か
、1〜3分間の間に液状態から固体に変化するフォーム
原料に上記のような異質物を悪影響を与えずに添加する
ことが不可能なため、有効発泡倍率への寄与の度合低下
を免れ得ないこと、2耐火物の添加、フォーム原料であ
る樹脂の使用量の増加に伴うコストアップを招くこと、
3耐火材の混入により可燃物の樹脂体を無理に難燃化す
るため発煙量が増加すること、4前記のような異質物は
合成樹脂発泡体中に平均に分散せしめることが比重、嵩
、大きさの関係で困難であり、逆に不均一分布は耐火性
の弱点部を大きくする。従つて全体の耐火性は低下する
ことになり、これらの解決が急務となつていた。また複
合パネルにおいて、その顔とも言うべき表面材の化粧面
に表面材ロール成形時に残留応力等により発生するオイ
ルキヤン(ペコツキ)が多数存在し、外観の低下あるい
は不良品率の増大を招く不利もあつた。本発明は、この
ような諸問題を簡単に解決せんと鋭意研究したものであ
る。
In general, the heat resistance of synthetic resin foams, such as polyurethane resins, is said to be around 100° C. under normal continuous use. However, despite its low heat resistance, it is widely used as a core material for building materials due to its excellent physical properties, such as being lightweight, self-adhesive, and processable. There is. Many methods for improving this heat resistance have been published to date, but a common drawback of these methods is that they lead to a decrease in the expansion ratio of the resin. By adding so-called foreign substances having different specific gravity, bulk, and shape, or by adding a flame retardant, the expansion ratio can be significantly lowered than that of the resin alone. In other words, the increase in the amount of foam raw material adhering to these foreign materials, the reaction, and the foaming is slight, and the above foreign materials have an adverse effect on the foam raw material, which changes from a liquid state to a solid within 1 to 3 minutes. Since it is impossible to add the foam without adding it, the degree of contribution to the effective expansion ratio inevitably decreases, and the addition of two refractories causes an increase in cost due to the increase in the amount of resin used as a foam raw material.
3. Mixing refractory materials forces the resin body of combustible materials to become flame-retardant, which increases the amount of smoke generated; 4. Distributing the above-mentioned foreign substances evenly in the synthetic resin foam increases specific gravity, bulk, This is difficult due to the size, and conversely, uneven distribution increases weak points in fire resistance. Therefore, the overall fire resistance is reduced, and there is an urgent need to solve these problems. In addition, in composite panels, there are many oil cans (pekotsuki) that occur on the decorative surface of the surface material, which can be called the face, due to residual stress etc. during roll forming of the surface material, which is disadvantageous because it deteriorates the appearance and increases the rate of defective products. It was hot. The present invention is the result of extensive research aimed at easily solving these problems.

その第一の目的は耐火性のグレードアップ、第二の目的
は上記した1〜4を最小限にくいとめることであり、第
三の目的は表面材のオイルキャンの抑制とパネルの機械
強度の改善である。以下に図面を用いて、本発明に係る
複合パネルについて詳細に説明する。
The first purpose is to upgrade the fire resistance, the second purpose is to minimize the problems 1 to 4 above, and the third purpose is to suppress oil can on the surface material and improve the mechanical strength of the panel. It is. The composite panel according to the present invention will be explained in detail below using the drawings.

第1図は本発明に係る複合パネルの横断面略図を示す。
図において、1は表面材で例えば表面処理鋼板、アルミ
ニウム板、銅板、ステンレス板等の金属薄板からなり、
その化粧面2に多数の凹凸3を成形する。
FIG. 1 shows a schematic cross-sectional view of a composite panel according to the invention.
In the figure, 1 is a surface material made of a thin metal plate such as a surface-treated steel plate, an aluminum plate, a copper plate, a stainless steel plate, etc.
A large number of irregularities 3 are formed on the decorative surface 2.

この凹凸の形状は第2図に拡大して示すように半球(図
示)、長方形、四角形、円形、その他不規則な形状等(
図示せず)であり、これらの一種以上をアトランダムに
あるいはシステマテツクに配設する。上記凹凸は耐火性
粒状物を安定した位置に確実に存在せしめると共に、オ
イルキヤンの見掛け上の抑制をも兼ねて配設したもので
ある。さらに凹凸状を形成した表面材は加工硬化による
剛性の増大と断面係数が大きくなることによる曲げ応力
の上昇が得られる。換言すると機械強度(曲げ強度、せ
ん断強さ)は平板状物より強くなり、長尺(12尺)に
なつた際は座屈に対しても強くなる。なお、この凹凸は
高低差が約1cfrL程度までであり、好ましくは0.
3〜0.7mm位である。4は耐火層で断熱性と耐火性
の向上および化粧面に対するバツクアツプ材として機能
する。
As shown in the enlarged view in Figure 2, the shape of this unevenness can be a hemisphere (as shown), a rectangle, a square, a circle, or other irregular shapes (
(not shown), and one or more of these may be arranged randomly or systematically. The above-mentioned irregularities are provided to ensure that the refractory granules are present in a stable position, and also to apparently suppress the oil can. Furthermore, the surface material with the uneven shape can increase the rigidity due to work hardening and increase the bending stress due to the increase in the section modulus. In other words, the mechanical strength (bending strength, shear strength) is stronger than that of a flat plate, and when it becomes long (12 shaku), it becomes strong against buckling. Note that the height difference of this unevenness is up to about 1 cfrL, preferably 0.
It is about 3 to 0.7 mm. 4 is a fireproof layer that improves heat insulation and fire resistance and functions as a backup material for decorative surfaces.

その具体例は第2図a−dに一部を拡大して示すように
一層あるいは二層以上(図示せず)設ける。すなわち、
a図は耐火層4が耐火性粒状物5の1種、無機質多孔粒
5aと無機材6の1種である加熱により発泡する無機材
6aとから構成した場合、b図は耐火層4が無機質多孔
粒5aおよび特殊パーライト粒5b、所謂耐火性粒状物
5と上記無機材6aとから構成した場合、c図は耐火層
4が無機質多孔粒5aと無機材6の1種であるガラス繊
維6bとから構成した場合、d図は耐火層4がb図に示
す耐火層4にさらにガラス繊維6bを混在させた場合で
ある。なお、加熱により発泡する無機材6a、ガラス繊
維6bは無機質多孔粒5a、または特殊パーライト粒5
b間にのみ介在させ、後記する樹脂の反応にあまり悪影
響を与えないように介在させる。さらに詳説すると、無
機質多孔粒5aはパーライト粒、焼成バーミキュラィト
、シラスバルーンからなり、特殊パーライト粒5bは上
記無機質多孔粒5aの表面あるいは内部空隙に高温下で
発泡する無機材、発泡しない無機材の一種以上を含浸、
半含浸、充填したもの、もしくはこれら表面にPVA.
CMC、アクリル樹脂、アルキツド樹脂、パラフイン等
の樹脂コーティングした粒状物である。さらに説明する
と、加熱により発泡する無機材6aとしては硅酸ソーダ
粉末、メタ硅酸ソーダ、硼酸ソーダ、メタ硼酸ソーダ、
硼砂およびこれらの一種以上を混合した水化物、または
これらの中間生成混合物である。なお、中間生成混合物
とはXNa2O・YB263・ZH2Oの三成分を適宜
に組合せたものである。また、x、Y.zは係数である
。この種無機材は、高温にさらされると結晶水を放出す
ると共に、次第に発泡膨脹して無機質発泡層を形成し、
可燃な合成樹脂を保護する。また、発泡しない無機材と
しては炭酸ナトリウム、重炭酸ナトリウム、硫酸カルシ
ウム、水酸化カルシウム、水酸化アルミニウム、ミヨウ
バン、硼酸亜鉛、ケイソー土、カオリンクレ一等であり
、この物質は高温下における結晶水の補給、無機質多孔
粒5aの変動防止、所謂、合成樹脂原料の反応、発泡時
に比重0.3程度の軽量物は通常合成樹脂原料の発泡圧
によつて大幅に移動するし、嵩の増大を抑制するが、軽
量物の移動を無機材によつて適当におさえて耐火粒状物
、無機材を添加した割に軽量化を図つたものである。な
お、この種物質を無機質多孔粒に含浸、半含浸、充填す
るには、100℃以下で溶融する物質あるいは、水に溶
ける物質は溶融状態にして多孔粒の表面、気孔および気
孔を通つて内部空隙に存在させる。また、目的に応じて
含浸、半含浸、充填を行う。そして含浸とは、無機質多
孔粒5aの表面の気孔部等にのみ付着したコーテイング
状態のものを意味し、半含浸とは無機質多孔粒5aの内
部空隙の半分程度まで前記物質が存在する状態である。
また充填とは、無機質多孔粒5aの全空隙に前記物質を
存在せしめた状態のものを意味する。7は合成樹脂発泡
体層で、合成樹脂原料が発泡の際に、その自己接着性を
介して構成物を一体に固着する。
A specific example thereof is provided with one layer or two or more layers (not shown), as partially enlarged in FIGS. 2a to 2d. That is,
Figure a shows a case where the fireproof layer 4 is composed of one type of refractory granules 5, inorganic porous particles 5a, and an inorganic material 6a that foams when heated, which is a type of inorganic material 6. Figure b shows a case where the fireproof layer 4 is composed of an inorganic material. When composed of porous grains 5a and special pearlite grains 5b, so-called refractory granules 5, and the above-mentioned inorganic material 6a, Fig. c shows that the refractory layer 4 is composed of inorganic porous grains 5a and glass fiber 6b which is one type of inorganic material 6. Figure d shows the case where the fireproof layer 4 shown in figure b is further mixed with glass fibers 6b. In addition, the inorganic material 6a and the glass fiber 6b that foam when heated are inorganic porous particles 5a or special pearlite particles 5.
It is interposed only between b and in such a way that it does not have too much of an adverse effect on the reaction of the resin, which will be described later. More specifically, the inorganic porous grains 5a are made of pearlite grains, fired vermiculite, and shirasu balloons, and the special pearlite grains 5b are inorganic materials that foam at high temperatures or non-foaming materials on the surface or internal voids of the inorganic porous grains 5a. impregnated with one or more of
Semi-impregnated, filled, or coated with PVA.
It is a granular material coated with resin such as CMC, acrylic resin, alkyd resin, paraffin, etc. To explain further, examples of the inorganic material 6a that foams upon heating include sodium silicate powder, sodium meta-silicate, sodium borate, sodium meta-borate,
Borax, a hydrated mixture of one or more of these, or an intermediate mixture thereof. Note that the intermediate product mixture is an appropriate combination of three components: XNa2O, YB263, and ZH2O. Also, x, Y. z is a coefficient. When this type of inorganic material is exposed to high temperatures, it releases crystal water and gradually foams and expands to form an inorganic foam layer.
Protect flammable synthetic resin. In addition, non-foaming inorganic materials include sodium carbonate, sodium bicarbonate, calcium sulfate, calcium hydroxide, aluminum hydroxide, alum, zinc borate, diatomaceous earth, and kaolin clay, which are used to replenish crystallized water at high temperatures. , Prevention of fluctuation of the inorganic porous particles 5a, so-called reaction of the synthetic resin raw material, lightweight materials with a specific gravity of about 0.3 during foaming usually move significantly due to the foaming pressure of the synthetic resin raw material, and suppress the increase in bulk. However, the movement of lightweight materials is appropriately suppressed using inorganic materials, and the weight is reduced despite the addition of refractory granules and inorganic materials. In addition, in order to impregnate, semi-impregnate, or fill inorganic porous particles with this kind of substance, substances that melt at 100°C or less or substances that are soluble in water should be melted and passed through the surface, pores, and pores of the porous particles to the interior of the porous particles. exist in the void. Also, impregnation, semi-impregnation, and filling are performed depending on the purpose. Impregnated means a state of coating that adheres only to the pores on the surface of the inorganic porous grains 5a, and semi-impregnated means a state in which the substance is present up to about half of the internal voids of the inorganic porous grains 5a. .
Moreover, filling means a state in which the substance is present in all the voids of the inorganic porous particles 5a. Reference numeral 7 denotes a synthetic resin foam layer, which fixes the components together through its self-adhesive properties when the synthetic resin raw material is foamed.

この合成樹脂としては、熱硬化性、好ましくはポリウレ
タン樹脂の如き常温硬化型である。8は裏面材でシート
状物、例えばアルミ箔、紙と金属箔をラミネートしたも
の、石綿紙、石綿紙とアルミ箔をラミネートしたシート
状物等である。
This synthetic resin is thermosetting, preferably room temperature curing type such as polyurethane resin. Reference numeral 8 denotes a sheet-like backing material, such as aluminum foil, a laminate of paper and metal foil, asbestos paper, a sheet-like material made of a laminate of asbestos paper and aluminum foil, and the like.

次に実施例につき説明する。実施例 1 ポリウレタン樹脂 100重量部 無機質多孔粒(パーライト粒、平 ,。Next, an example will be explained. Example 1 polyurethane resin 100 parts by weight Inorganic porous grains (pearlite grains, flat,.

重量部均粒径3mmφ)無機材(硼砂、平均150メツ
シ ゛ 20重量部 ユ) そこで鉄板(0,3mTIL)の上に、第2図に示す如
き半球状凹凸(深さ0.7mm)を形成し、その上にパ
ーライト粒5aおよびパーライト粒5a間の空隙に硼砂
6aを介在して耐火層を第2図aに示すように形成する
Inorganic material (borax, average grain size 3 mmφ) (borax, average particle size 150 mesh, 20 parts by weight) Therefore, hemispherical irregularities (depth 0.7 mm) as shown in Fig. 2 were formed on an iron plate (0.3 m TIL). Then, a refractory layer is formed thereon by interposing pearlite grains 5a and borax 6a in the spaces between the pearlite grains 5a, as shown in FIG. 2a.

次に、その上に上記原料を吐出積層し、その上に0.3
m77!厚の不燃シート状物(アスベスト紙とアルミニ
ウム箔からなるもの)を重ね、それをキヤタピラ式の成
形機(図示せず)を介して加温、加圧して、第1図に示
す如き断面に形成し、その厚さが10mmのパネルに製
造した。
Next, the above raw material is discharged and laminated on top of it, and 0.3
m77! Thick noncombustible sheet materials (made of asbestos paper and aluminum foil) are stacked and heated and pressurized using a caterpillar type molding machine (not shown) to form the cross section shown in Figure 1. A panel with a thickness of 10 mm was manufactured.

そこで、このパネルの鉄板面を火炎に向けて準不燃(J
IS−A一1321)の表面試験を行なつたところ合格
する特性を得た。実施例 2 配合比 これら構成材を第2図eの構造に配設した。
Therefore, we aimed the steel plate side of this panel toward the flame and
When the surface test of IS-A-11321) was conducted, the characteristics were found to pass. Example 2 Mixing Ratio These components were arranged in the structure shown in FIG. 2e.

なお、パーライト粒5aと、特殊パーライト粒5bは混
在し、その粒状物間にガラス繊維6bを介在したもので
ある。そこで、これを実施例1と同様に火炎にさらした
ところ準不燃材に合格する性能を示した。しかも、この
場合はパーライト粒5bに含浸したメタ硼酸ソーダが5
4℃位から溶融してパーライト粒5aから流出し始める
Note that the pearlite grains 5a and special pearlite grains 5b are mixed, and glass fibers 6b are interposed between the grains. Therefore, when this was exposed to flame in the same manner as in Example 1, it exhibited performance that passed the test as a quasi-noncombustible material. Moreover, in this case, the sodium metaborate impregnated into the pearlite grains 5b is
It melts from about 4° C. and begins to flow out from the pearlite grains 5a.

そして不燃ガス(水蒸気)を大量に放出すると共に、次
第に粘稠になり、120〜160℃で発泡し始めパーラ
イト粒5a間をガラス繊維を補強材として混入した無機
質発泡層で橋絡し、鉄板と樹脂発泡層間に断熱不燃の耐
火発泡層を形成し、十分な耐火性能を示した。なお、実
施例1、2と従来例のJIS−A−1321における特
性を下表に示す。また、従来例とはポリウレタンフオー
ム内にパーライト5aのみを20重量部平均に分散した
フオームを芯材とする複合パネルである。以上説明した
のは、本発明の一実施例にすぎず、接着剤を塗布し、そ
の後で耐火性粒状物を敷設してもよい。
Then, as a large amount of non-flammable gas (water vapor) is released, it gradually becomes viscous and begins to foam at 120 to 160°C, and the pearlite grains 5a are bridged with an inorganic foam layer mixed with glass fiber as a reinforcing material, and the iron plate and A heat-insulating, non-combustible, fire-resistant foam layer was formed between the resin foam layers, demonstrating sufficient fire-resistance performance. The characteristics of Examples 1 and 2 and the conventional example according to JIS-A-1321 are shown in the table below. The conventional example is a composite panel whose core material is a polyurethane foam in which only pearlite 5a is dispersed in an average amount of 20 parts by weight. What has been described above is only one embodiment of the present invention, and the adhesive may be applied and then the refractory granules may be laid down.

また樹脂に周知の触媒、難燃剤等を添加することができ
る。その他、前記した特殊パーライト粒5bには必要に
より有機物質を含浸させることもできる。この有機物質
としてはPVA(ポリビニルアルコール)、CMC(カ
ルボキシメチルセルロース)、でんぷん等であり、前記
発泡する無機材、発泡しない無機材の含浸、充填量を目
的に応じて調節するものである。さらにこの有機物質は
、これら無機材の結晶水等の水分の低下を抑制する。上
述したように、本発明に係る耐火性を有する複合パネル
によれば、不燃基材に機械的補強と耐火・囲粒状物を安
定に支持するために凹凸を設けたため、見かけ上はオイ
ルキヤンによる不良率が勿んど無くなつた。
Furthermore, well-known catalysts, flame retardants, etc. can be added to the resin. In addition, the special pearlite grains 5b described above may be impregnated with an organic substance if necessary. The organic substances include PVA (polyvinyl alcohol), CMC (carboxymethylcellulose), starch, etc., and the impregnation and filling amount of the foaming inorganic material and non-foaming inorganic material are adjusted depending on the purpose. Furthermore, this organic substance suppresses a decrease in water content such as crystal water of these inorganic materials. As described above, according to the fire-resistant composite panel of the present invention, the unevenness is provided on the non-combustible base material in order to provide mechanical reinforcement and to stably support the fire-resistant/surrounding granular material, so that it appears that the oil can The defective rate has naturally disappeared.

また、耐火性粒状物を物理的に確実に固設して耐火層を
形成して可燃な樹脂発泡体の溶融、燃焼を抑制する。も
ちろん、耐火層を発泡体内に設けたため、これが増量材
、骨材的な作用効果をなし、芯材を高密度となし、可撓
性を抑制して剛性を相乗的作用によつて向上せしめ、オ
イルキャン発生原因の除去にも寄与している。
In addition, the refractory granules are physically firmly fixed to form a refractory layer, thereby suppressing melting and combustion of the flammable resin foam. Of course, since the fireproof layer is provided inside the foam, it functions as a filler and aggregate, making the core material high-density, suppressing flexibility and improving rigidity through a synergistic effect. It also contributes to eliminating the cause of oil can.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明に係る複合パネルの一実施例を示す断面
図、第2図a−dは第1図において4印で示した部分を
各別にそれぞれ抽出し、拡大して示す説明図である。 1・・・・・・表面材、3・・・・・・凹凸、4・・・
・・・耐火層、6・・・・・・無機材、8・・・・・・
裏面材。
FIG. 1 is a cross-sectional view showing an embodiment of the composite panel according to the present invention, and FIGS. 2 a to 2 d are explanatory diagrams showing the parts indicated by 4 marks in FIG. 1 separately and enlarged. be. 1...Surface material, 3...Irregularities, 4...
...Fireproof layer, 6...Inorganic material, 8...
Back material.

Claims (1)

【特許請求の範囲】[Claims] 1 金属板の少なくとも化粧面に小さな凹凸を形成した
表面材と、該化粧面の背面凹凸に一部埋没した状態に敷
設した耐火性粒状物および該粒状物間にのみ介在させる
無機材とからなる耐火層と、該粒状物の上に積層すると
共に不燃性基材からなる裏面材および上記表面材、粒状
物をその自己接着性により一体に固着してなる合成樹脂
発泡体層とから構成したことを特徴とする耐火性を有す
る複合パネル。
1 Consisting of a surface material with small irregularities formed on at least the decorative surface of a metal plate, refractory granules laid partially buried in the irregularities on the back surface of the decorative surface, and an inorganic material interposed only between the granules. It is composed of a fireproof layer, a synthetic resin foam layer that is laminated on the granular material and is made of a backing material made of a noncombustible base material, and the surface material and the granular material are fixed together by their self-adhesive properties. A composite panel with fire resistance.
JP14439280A 1980-10-17 1980-10-17 Composite panel with fire resistance Expired JPS5930543B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14439280A JPS5930543B2 (en) 1980-10-17 1980-10-17 Composite panel with fire resistance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14439280A JPS5930543B2 (en) 1980-10-17 1980-10-17 Composite panel with fire resistance

Publications (2)

Publication Number Publication Date
JPS5658851A JPS5658851A (en) 1981-05-22
JPS5930543B2 true JPS5930543B2 (en) 1984-07-27

Family

ID=15361075

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14439280A Expired JPS5930543B2 (en) 1980-10-17 1980-10-17 Composite panel with fire resistance

Country Status (1)

Country Link
JP (1) JPS5930543B2 (en)

Also Published As

Publication number Publication date
JPS5658851A (en) 1981-05-22

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