JPS582814B2 - Nannensei Hatsupouzaino Seizouhouhou - Google Patents
Nannensei Hatsupouzaino SeizouhouhouInfo
- Publication number
- JPS582814B2 JPS582814B2 JP753279A JP327975A JPS582814B2 JP S582814 B2 JPS582814 B2 JP S582814B2 JP 753279 A JP753279 A JP 753279A JP 327975 A JP327975 A JP 327975A JP S582814 B2 JPS582814 B2 JP S582814B2
- Authority
- JP
- Japan
- Prior art keywords
- foam
- raw material
- resin
- pearlite
- added
- 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
Links
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
Description
【発明の詳細な説明】
本発明は、耐火、耐熱性に富むパーライト粒を温度によ
ってその反応速度等が触媒のごとく大きく影響を受ける
独立気泡組織のポリウレタンフォームを形成する原料に
、その反応を阻害することなしに添加して、難燃性を改
善したポリウレタンフォームの製造方法に関する。Detailed Description of the Invention The present invention utilizes pearlite grains, which are highly fire and heat resistant, as a raw material for forming polyurethane foam with a closed cell structure, the reaction rate of which is greatly affected by temperature, like a catalyst. The present invention relates to a method for producing polyurethane foam with improved flame retardancy by adding the polyurethane foam without adding any additives.
ポリウレタン樹脂からなる発泡体(以下、単にフォーム
という)は、易燃性であると共に、化学反応が急激で、
かつ反応系は温度に極めて敏感な物質であることが知ら
れている。Foamed materials made of polyurethane resin (hereinafter simply referred to as foam) are easily flammable and undergo rapid chemical reactions.
It is also known that the reaction system is a substance that is extremely sensitive to temperature.
特に発泡剤としてフレオン11、クレオン12等を用い
た独立気泡組織を形成するフォームの原料はより敏感で
ある。In particular, raw materials for foams that form closed cell structures using Freon 11, Creon 12, etc. as blowing agents are more sensitive.
また、この種樹脂は超断熱性を発揮すること、および基
材等の形状に関係なく注入、吐出が容易なことなどのた
めに建材等に多用されつつある。In addition, this type of resin is increasingly being used for building materials and the like because it exhibits super-insulating properties and is easy to inject and discharge regardless of the shape of the base material.
そして、フォームの難燃化を図る為には耐火、耐熱性の
パーライト粒を添加することが行なわれている。In order to make the foam flame retardant, fire-resistant and heat-resistant pearlite grains are added.
しかしながら、ポリウレタン樹脂は温度の影響が発熱、
反応系において触媒のように作用するため、その反応途
中に単なるパーライト粒、所謂外気温のパーライト粒を
添加すると当然に種々の不利が生ずる。However, polyurethane resin is affected by temperature and generates heat.
Since it acts like a catalyst in the reaction system, if mere pearlite particles, so-called ambient temperature pearlite particles, are added during the reaction, various disadvantages will naturally occur.
すなわち、■外気温状態のパーライト粒を反応途中の原
料にその3割以上(重量比)を添加した場合には反応速
度、粘度、発泡タイミングを所期の設定に対し大きく変
化させる間題がある。In other words, if more than 30% (by weight) of pearlite particles at ambient temperature are added to the raw material in the middle of reaction, there is a problem that the reaction rate, viscosity, and foaming timing will change significantly from the intended settings. .
特に厳寒の冬では、パーライト粒が屋内でも通常5〜1
0℃であり、反応途中の原料が30〜40℃であるため
反応がパーライト粒添加部分だけ部分的に冷却し、反応
速度を不均一にすると共に発泡前の発泡剤における気化
のタイミングと粘度とをも乱し、発泡組織をひどく荒ら
す。Especially in the bitterly cold winter, perlite grains are usually 5 to 1 even indoors.
Since the temperature of the raw material during the reaction is 30 to 40°C, the reaction only partially cools the area where the pearlite particles are added, making the reaction rate uneven, and also affecting the timing and viscosity of vaporization of the blowing agent before foaming. It also disturbs the foam structure and severely damages the foam structure.
従って、フォームはバラバラな発泡密度となり、ボイド
の発生、連通化により発泡倍率が低下すると共に、発泡
組織が一部破壊される。Therefore, the foam has a varying density, the foaming ratio decreases due to the generation and communication of voids, and the foam structure is partially destroyed.
従って、フォームの機械強度はひどく低下する。The mechanical strength of the foam is therefore severely reduced.
もちろん、パーライト粒が僅少量の場合は無視できるが
、難燃性を得る程の量が添加されたときは上記のような
結果を免れ得なかった。Of course, if the pearlite particles are in a small amount, they can be ignored, but when they are added in an amount sufficient to provide flame retardance, the above results cannot be avoided.
■また、反応速度が部分的に狂わされるため樹脂の反応
状態もバラバラになり、接着性度合が不斎一になって全
体としての接着性が劣化される。(2) Furthermore, since the reaction rate is partially disturbed, the reaction state of the resin becomes inconsistent, and the degree of adhesion becomes unsatisfactory, resulting in a deterioration of the overall adhesion.
■パーライト粒を樹脂の反応熱で樹脂の反応温度と同等
まで上昇せしめるには相当の熱量が必要であり、樹脂の
性状の急速な変化にパーライト粒表面の加温が追従でき
ず、逆に反応速度を狂わすことになる。■It takes a considerable amount of heat to raise the pearlite grains to the same level as the reaction temperature of the resin, and the surface heating of the pearlite grains cannot keep up with the rapid changes in the properties of the resin, causing the reaction to occur in the opposite direction. It will slow you down.
■パーライト粒は吸油性が有りパーライト粒を例えば二
液反応型の未発泡のポリウレタン樹脂に混合せしめると
、その吸油性によって樹脂分が大幅に減少する。(2) Pearlite particles have oil absorption properties, and when pearlite particles are mixed with, for example, a two-component reaction type unfoamed polyurethane resin, the resin content is significantly reduced due to its oil absorption properties.
従つて、供給された樹脂分に比して発泡倍率が低下する
ことになる。Therefore, the foaming ratio will be lower than the resin content supplied.
これは、ポリウレタン樹脂A1B原液を混合した状態で
は油性であり、これに吸油性の強い多数の気孔を表面に
有するパーライト粒を添加、混合すると、パーライト粒
により低粘度で流動性に富む樹脂が多数の気孔から吸収
されるためである。This is oily when mixed with the polyurethane resin A1B stock solution, and when pearlite grains with a large number of highly oil-absorbing pores on the surface are added and mixed, the pearlite grains create a large number of resins with low viscosity and high fluidity. This is because it is absorbed through the pores of the body.
なお、吸収される量を予め付加した原料吐出としなけれ
ばならない不利がある。Note that there is a disadvantage that the amount of material to be absorbed must be added beforehand to the discharged material.
しかも、この種原料は高価であり、このことが製品のコ
ストアップに直接影響するものである。Moreover, this kind of raw material is expensive, which directly affects the increase in the cost of the product.
勿論吐出量を低減すれば、フォームに種々の凹凸、収縮
が生じ、とても製品になり得ない。Of course, if the discharge rate is reduced, various irregularities and shrinkage will occur in the foam, making it impossible to produce a product.
■また、このような欠点を除去せんとして、触媒を使用
した場合は、これ自体高価であり、かつ前記したような
反応が部分的であるため、殆んど無駄になる。(2) Furthermore, if a catalyst is used in an attempt to eliminate such drawbacks, it is expensive in itself, and the reaction described above is only partial, so it is almost useless.
■フォームの発泡組織が実用不可能の状態で難燃化を図
っても意味がない。■There is no point in trying to make the foam flame retardant when the foam structure is impractical.
■特にフォームに対しこの種パーライト粒を大量に添加
するとフォームの断熱性がひどく低下すると共に、樹脂
の使用量が増加する等の欠点があった。(2) In particular, when a large amount of pearlite particles of this kind are added to a foam, there are drawbacks such as a severe decrease in the insulation properties of the foam and an increase in the amount of resin used.
本発明はこのような欠点を除去するため、パーライト粒
を加温、例えば原料の加温温度以上に加温して添加し、
このパーライト粒が反応途中の樹脂との出合いにおいて
、その熱によりパーライト粒表面に付着した樹脂分を急
激に反応膨脹せしめて樹脂粘度を短時間の間に上昇せし
め、パーライト粒の吸油性を遮断し、かつ他周囲への温
度の悪影響を阻止して所期の反応速度、発泡倍率を得る
と共に難燃性をも改善したフォームの製造方法を提案す
る。In order to eliminate such drawbacks, the present invention adds pearlite grains by heating them, for example, heating them to a temperature higher than the heating temperature of the raw material,
When these pearlite particles encounter resin during the reaction, the heat causes the resin adhering to the surface of the pearlite particles to react and expand rapidly, increasing the resin viscosity in a short period of time, blocking the oil absorption of the pearlite particles. The present invention proposes a method for producing foam that achieves the desired reaction rate and expansion ratio by preventing the adverse effects of temperature on other surroundings, and also improves flame retardancy.
以下に図面を用いて本発明に係る難燃性フォームの製造
方法について詳細に説明する。EMBODIMENT OF THE INVENTION Below, the manufacturing method of the flame retardant foam based on this invention is demonstrated in detail using drawing.
第1図は上記発明の実施に供する装置の→りを示す側面
図であり、1はフォーム、2,3は上、下の型部材で無
端の金属板あるいは無端帯に多数の分割型部片を連結し
て発泡体1を対面して挾持し、一定厚さの型4を形成す
る。FIG. 1 is a side view of the apparatus used for carrying out the above invention, in which 1 is a form, 2 and 3 are upper and lower mold members, and an endless metal plate or an endless band is made up of a large number of divided mold parts. are connected and sandwiched with the foam 1 facing each other to form a mold 4 having a constant thickness.
なお、型の高さは前記フォームの自然発泡高さより小さ
い間隙に設定する。Note that the height of the mold is set to a gap smaller than the natural foaming height of the foam.
56は案内輪、?,8は駆動輪で上記上下型部材を巻掛
するものであり、9,10は補助輪で型40部分で上下
に向い合った型部材2,3を支持する。56 is a guide wheel, ? , 8 are drive wheels that wrap around the upper and lower mold members, and 9 and 10 are auxiliary wheels that support the mold members 2 and 3 facing each other vertically at the mold 40 portion.
11,12は温度制御装置で上記各型部材2,3に向っ
て加熱空気を吹付けるダクトを備え、樹脂原料の養生を
短時間に行なうものである。Reference numerals 11 and 12 denote temperature control devices which are equipped with ducts for blowing heated air toward the respective mold members 2 and 3, thereby curing the resin raw material in a short time.
13は例えばキャタピラ式の成形機で、上記型部材2,
3、案内輪5,6、駆動輪7,8、補助輪9,10、温
度制御装置11,12から構成されている。13 is a caterpillar type molding machine, for example, and the mold members 2,
3, guide wheels 5, 6, drive wheels 7, 8, auxiliary wheels 9, 10, and temperature control devices 11, 12.
なお下型部材3は図から明らかなように型4が移動する
方向と逆方向(図では左)に延びている。As is clear from the figure, the lower die member 3 extends in a direction opposite to the direction in which the die 4 moves (to the left in the figure).
14はフォーム原料供給機で型40入口に対し前方の適
所に設置する。Reference numeral 14 denotes a foam raw material feeder, which is installed at a suitable location in front of the mold 40 entrance.
この供給機はその原料であるポリイソシアネートとポリ
オールとを独立して収容した槽15,16を混合機17
に連結してなる。This feeder connects tanks 15 and 16 that separately contain polyisocyanate and polyol, which are the raw materials, to a mixer 17.
It becomes connected to.
18はパイブレータ、ミキサーなどのパーライト粒散布
機でその上部に加温装置19が連結されている。Reference numeral 18 denotes a perlite grain dispersing machine such as a pipebrator or a mixer, and a heating device 19 is connected to the upper part thereof.
この加温装置19はヒータあるいは円筒体に火炎雰囲気
を作りこの中を短時間通過することにより約20〜80
℃に骨材を加温するものである。This heating device 19 creates a flame atmosphere in a heater or a cylindrical body and passes through it for a short period of time.
This heats the aggregate to ℃.
20は例えばパーライト粒、シラスバルーン、バーミキ
ュライトなどからなり、合成樹脂原料100重量部に対
し30〜200重量部添加する。20 is made of pearlite grains, shirasu balloons, vermiculite, etc., and is added in an amount of 30 to 200 parts by weight per 100 parts by weight of the synthetic resin raw material.
なお、上、下限を設定したのは、添加量が少量の場合そ
れほど悪影響を与えず、かつ難燃性も殆んど期待できな
いことになる。Note that the upper and lower limits are set because if the amount added is small, it will not have much of an adverse effect and almost no flame retardancy can be expected.
また、上限は樹脂量があまり少ないと、嵩の大きいパー
ライト粒を平均に混合できにくくなるためである。Further, the upper limit is set because if the amount of resin is too small, it becomes difficult to evenly mix large pearlite particles.
21は下側用基材(表面材)で金属板、石膏板、22は
上側用基材(裏面材)で例えばアルミ箔、防水紙、合成
樹脂フイルムなどからなる。21 is a base material for the lower side (surface material), such as a metal plate or a plaster board; 22 is a base material for the upper side (rear surface material), which is made of, for example, aluminum foil, waterproof paper, or synthetic resin film.
次に、本願発明の製造方法を説明すると、いま成形機1
3が矢印方向に回転し、左側から基材221が送給され
、下型部材3に載置されたと仮定する。Next, to explain the manufacturing method of the present invention, the molding machine 1
3 is rotated in the direction of the arrow, and the base material 221 is fed from the left side and placed on the lower mold member 3.
そこで基材21が混合機17の下に到来するとその平面
上に樹脂混合物23が散布(吐出)される。When the base material 21 arrives under the mixer 17, the resin mixture 23 is spread (discharged) onto the plane thereof.
この面が骨材散布機18の下に到来すると例えば25〜
80℃に加温装置19によって加温されたパーライト粒
が落下、散布(バラマキもありうる)される。When this surface arrives under the aggregate spreader 18, for example, 25~
Pearlite grains heated to 80° C. by the heating device 19 are dropped and scattered (sometimes scattered).
なお、100℃以上になると樹脂自体の反応にスコーチ
等の悪影響が考えられる。Note that if the temperature exceeds 100°C, there may be an adverse effect such as scorch on the reaction of the resin itself.
次にこの上に基材22が載置され成形機13を経て型4
の出口から難燃性フォームとして送出される。Next, a base material 22 is placed on top of this and passed through a molding machine 13 into a mold 4.
from the outlet as flame retardant foam.
そこで、このフォームを切断し、観察したところ、■発
泡組織が荒れておらず、独立気泡の均質セル構造が形成
されていた。Then, when this foam was cut and observed, it was found that (1) the foam structure was not rough and a homogeneous cell structure of closed cells was formed.
■パーライト粒は殆んど樹脂を吸油せず、かつその表皮
に樹脂の急激な反応発泡でうすいスキン層が形成された
跡が見られた。■The pearlite grains hardly absorbed any resin, and there were signs that a thin skin layer had been formed on the surface of the pearlite particles due to rapid reaction foaming of the resin.
しかし、その周りの発泡組織への影響は見られなかった
。However, no effect on the surrounding foam structure was observed.
■発泡倍率は原料単体の発泡より幾分低下するほどであ
り、加温しないで添加した場合に比し、はるかに高かっ
た。(2) The expansion ratio was slightly lower than that of the raw material alone, and was much higher than when it was added without heating.
また難燃性は難燃3級程度の性能が得られた。In addition, flame retardancy was approximately 3rd class flame retardant.
■機械強度は従前に比し、向上した。■Mechanical strength has improved compared to before.
■フォームには欠陥部位(ボイド)が認められなかった
。■No defective areas (voids) were observed in the foam.
ここで、これらをより明確にするため実施例を示す。Here, an example will be shown to make these more clear.
実施例1
配合比
ポリウレタン樹脂 100重量部パーラ
イト粒(平均粒径3mmφ) 30重量部そこでポ
リウレタン樹脂原料(ポリオールとポリイソシアネート
)を各々20℃に加温し、1:1の割合で混合して加温
された型上に吐出する。Example 1 Compounding ratio Polyurethane resin 100 parts by weight Pearlite grains (average particle size 3 mmφ) 30 parts by weight Then, polyurethane resin raw materials (polyol and polyisocyanate) were each heated to 20°C, mixed at a ratio of 1:1, and heated. Dispense onto warmed molds.
そして、この原料が反応、例えばクリームタイム時に6
0℃に加温されたパーライト粒を添加し、フリー発泡さ
せた。Then, this raw material reacts, for example, at cream time, 6
Perlite particles heated to 0° C. were added to allow free foaming.
この場合のカサ比重は0.0480g/cm3、なおこ
の配合でパーライトの温度を10℃、25℃、80℃に
変化した場合のカサ比重をグラフで示すと第2図におげ
る■のようになる。In this case, the bulk specific gravity is 0.0480 g/cm3, and the graph of the bulk specific gravity when the pearlite temperature is changed to 10℃, 25℃, and 80℃ with this mixture is shown in Figure 2. become.
実施例2
配合比
ポリウレタン樹脂 100重量部パーラ
イト粒(平均粒径3mmφ) 50重量部これを実
施例1と同一条件でフォームを製造した。Example 2 Compounding ratio: Polyurethane resin: 100 parts by weight Perlite particles (average particle size: 3 mmφ): 50 parts by weight A foam was produced using this under the same conditions as in Example 1.
この場合も実施例1と同じようにパーライト粒の温度を
変化したときのカサ比重を第2図@に示す。In this case, as in Example 1, the bulk specific gravity when the temperature of the pearlite grains is varied is shown in FIG. 2@.
比較例1
配合比
ポリウレタン樹脂 1oo重量部パーラ
イト粒(平均粒径3mmφ) 10重量部この成分を
実施例1と同じように添加混合し、フリー発泡体を製造
した。Comparative Example 1 Compounding ratio Polyurethane resin 10 parts by weight Perlite grains (average particle size 3 mmφ) 10 parts by weight These components were added and mixed in the same manner as in Example 1 to produce a free foam.
この場合もパーライト粒の添加温度を変化せしめたとき
のカサ比重の特性を第2図θに示す。In this case as well, the characteristics of the bulk specific gravity when the addition temperature of pearlite grains is varied are shown in FIG. 2 θ.
第2図から明らかなように、パーライト粒の添加量が少
ない場合はそれほどカサ比重を低減せしめないが、増加
するに従って顕著に影響することが解る。As is clear from FIG. 2, when the amount of pearlite grains added is small, the bulk specific gravity is not reduced so much, but as it increases, the effect becomes more pronounced.
以上説明したのは本発明の一実施例にすぎず、その他の
無機粉粒物、例えば硼砂、メタ硼酸ソーダなどの硼酸化
合物、硅酸化合物、炭酸塩などをパーライト粒供給機1
90前後に設置したりすることもできる。What has been described above is only one embodiment of the present invention, and other inorganic powder and granules such as borax, boric acid compounds such as sodium metaborate, silicic acid compounds, carbonates, etc.
It is also possible to set it around 90.
上述したように、本発明に係る難燃性フォームの製造方
法によれば、添加物表面の熱によって熱に敏感に反応す
るフォーム原料を直ちに発泡させ、吸油性のパーライト
粒の表面を包囲し、発泡倍率に悪影響を与える吸油性を
最小範囲内で遮断し、最良の発泡倍率で難燃性フォーム
を安価に製造できる大きな特徴がある。As described above, according to the method for producing flame-retardant foam according to the present invention, the foam raw material that reacts sensitively to heat is immediately foamed by the heat on the surface of the additive, and the surface of the oil-absorbing pearlite grains is surrounded. A major feature of this method is that oil absorption, which adversely affects the expansion ratio, can be blocked to a minimum extent, and flame-retardant foam can be manufactured at low cost with the best expansion ratio.
また樹脂反応発泡状態を阻害することなしに加温された
パーライト粒を添加するため従前の如き高価な触媒を使
用する必要がなくコストを大幅に低減できる。Furthermore, since the heated pearlite particles are added without inhibiting the resin reaction foaming state, there is no need to use an expensive catalyst as in the past, and costs can be significantly reduced.
また本発明によれば、均質な発泡組織を得ることができ
る特徴がある。Further, according to the present invention, a homogeneous foamed structure can be obtained.
第1図は本発明の実施に供する装置を示す側面図、第2
図は本発明に係る製造方法によって製造した際の発泡体
のカサ比重を示す特性線図である。
1・・・・・・発泡体、2,3・・・・・・型部材、4
・・・・・・型、13・・・・・・成形機、17・・・
・・・混合機、18・・・・・・パーライト散布機、1
9・・・・・・加熱装置、20・・・・・・骨材、21
,22・・・・・・基材。Fig. 1 is a side view showing an apparatus for carrying out the present invention;
The figure is a characteristic diagram showing the bulk specific gravity of a foam produced by the production method according to the present invention. 1... Foam, 2, 3... Mold member, 4
...Mold, 13...Molding machine, 17...
... Mixer, 18 ... Perlite spreader, 1
9... Heating device, 20... Aggregate, 21
, 22...Base material.
Claims (1)
ウレタン樹脂原料にパーライト粒を添加し、上記原料を
反応、発泡せしめて所定形状の独立気泡組織からなる難
燃性ポリウレタンフォームを製造するに当り、前記原料
がクリームタイム状態のときに原料100重量部に対し
て約25〜80℃に加温したパーライト粒を30重量部
以上添加したことを特徴とする難燃性ポリウレタンフォ
ームの製造方法。1. When producing a flame-retardant polyurethane foam consisting of a closed cell structure of a predetermined shape by adding pearlite particles to a polyurethane resin raw material whose reaction rate and viscosity rapidly change depending on temperature, and causing the raw material to react and foam, the above-mentioned A method for producing flame-retardant polyurethane foam, characterized in that 30 parts by weight or more of perlite particles heated to about 25 to 80°C are added to 100 parts by weight of the raw material when the raw material is in a cream time state.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP753279A JPS582814B2 (en) | 1974-12-27 | 1974-12-27 | Nannensei Hatsupouzaino Seizouhouhou |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP753279A JPS582814B2 (en) | 1974-12-27 | 1974-12-27 | Nannensei Hatsupouzaino Seizouhouhou |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5177667A JPS5177667A (en) | 1976-07-06 |
| JPS582814B2 true JPS582814B2 (en) | 1983-01-18 |
Family
ID=11552971
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP753279A Expired JPS582814B2 (en) | 1974-12-27 | 1974-12-27 | Nannensei Hatsupouzaino Seizouhouhou |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS582814B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60500085A (en) * | 1982-12-22 | 1985-01-24 | シユミツト,ジヨン | Building materials for building elements and their manufacturing methods and manufacturing equipment |
-
1974
- 1974-12-27 JP JP753279A patent/JPS582814B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5177667A (en) | 1976-07-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3274046A (en) | Combined fiber and cellular article | |
| JPH10502415A (en) | Extruded polymer foam with filler particles and method | |
| US5798064A (en) | Process and apparatus for fabrication of flexible foam | |
| JP2000302565A (en) | Foamed mineral building and structural material, production of mineral foamed body, and apparatus for executing the method | |
| JPS582814B2 (en) | Nannensei Hatsupouzaino Seizouhouhou | |
| US4900759A (en) | Phenolic foams | |
| US2576911A (en) | Method of making cellular thermoplastic products | |
| KR101851691B1 (en) | Sound absorbing material for interlayer noise | |
| CN203808270U (en) | Polyurethane heat-insulating material | |
| JP2004090647A (en) | Manufacturing method of fireproof board | |
| JPS5821653B2 (en) | Method for manufacturing flame-retardant cold-curing plastic foam | |
| KR100940946B1 (en) | Manufacturing method of flameproof interior using waste styrofoam | |
| US4522954A (en) | Method for producing a low density foamed polyester resin | |
| JPH0114003B2 (en) | ||
| JPS61113629A (en) | Foamable composition and foamed material produced therefrom | |
| JPS6144046B2 (en) | ||
| JPS5930745B2 (en) | Fillers for fire-resistant building materials and compositions for fire-resistant building materials | |
| JPS593263B2 (en) | Molding equipment for fire-resistant foam material | |
| JPS5825374B2 (en) | Foaming agent for synthetic resin compounding | |
| JPS6234526B2 (en) | ||
| JPS606413Y2 (en) | Fire-resistant, heat-resistant synthetic resin foam | |
| JPS5947984B2 (en) | Fire-resistant, heat-resistant fiber laminate | |
| JPH0255573B2 (en) | ||
| JPS6141304B2 (en) | ||
| JPS5845464B2 (en) | Taikari Yuushi Oyobi Soreimochiitaika Taikari Taikari |