JPH0626622B2 - Fire spread inhibitor - Google Patents
Fire spread inhibitorInfo
- Publication number
- JPH0626622B2 JPH0626622B2 JP62211304A JP21130487A JPH0626622B2 JP H0626622 B2 JPH0626622 B2 JP H0626622B2 JP 62211304 A JP62211304 A JP 62211304A JP 21130487 A JP21130487 A JP 21130487A JP H0626622 B2 JPH0626622 B2 JP H0626622B2
- Authority
- JP
- Japan
- Prior art keywords
- water
- fire
- heat
- gel
- gel layer
- 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 - Lifetime
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- Fireproofing Substances (AREA)
Description
【発明の詳細な説明】 本発明は、火災時に燃焼物からの接炎及び放射熱によっ
て影響を受ける面に、粉粒体のヒドロキシプロピルメチ
ルセルロース、ヒドロキシエチルメチルセルロース等の
非イオン性の水溶性セルロースエーテル等に粉粒体のア
クリル酸重合物ナトリウム塩、デンプン−アクリル酸グ
ラフト共重合体等の高吸水性樹脂を添加混合させた薬剤
を用い、これに吸水させ生成されたゲルを燃焼物からの
接炎及び放射熱による影響を受ける面に付着させると、
ゲル内の温度が上昇し、ゲル内に含有されているヒドロ
キシプロピルメチルセルロース、ヒドロキシエチルメチ
ルセルロース等の非イオン性の水溶性セルロースエーテ
ル等が熱ゲル化し、より強固なゲル層となり、ガラス等
の表面が滑らかな垂直面にも容易にゲル層を形成させる
ことができることを特徴とした延焼抑制剤である。DETAILED DESCRIPTION OF THE INVENTION The present invention provides a nonionic water-soluble cellulose ether such as granular hydroxypropylmethyl cellulose and hydroxyethylmethyl cellulose on the surface which is affected by flame contact and radiant heat from a combustion product at the time of fire. , Etc., and a highly water-absorbing resin such as sodium salt of acrylic acid polymer in the form of granules, starch-acrylic acid graft copolymer, etc. were mixed and used, and the gel produced by absorbing water was contacted with the combusted material. When attached to the surface affected by flames and radiant heat,
The temperature inside the gel rises, and nonionic water-soluble cellulose ethers such as hydroxypropylmethylcellulose and hydroxyethylmethylcellulose contained in the gel are thermally gelled, forming a stronger gel layer, and the surface of glass etc. It is a fire spread inhibitor characterized in that a gel layer can be easily formed on a smooth vertical surface.
(従来の技術) 従来、火災時に燃焼物からの接炎、及び放射熱による延
焼を抑制する一般的に行われている手段としては、燃焼
物からの接炎及び輻射熱の影響を受ける面に、断続的ま
たは継続的な注水を行って冷却し、延焼を抑制している
ところである。(Prior Art) Conventionally, as a generally-used means for suppressing flame contact from a combustion product at the time of a fire and spread of heat by radiant heat, a surface affected by the flame contact from the combustion product and radiant heat, We are injecting water intermittently or continuously to cool and suppress the spread of fire.
また、注水させた水が放射熱によって気化することを遅
延させ延焼を防止する方法として、水とアクリル酸重合
体、または水とアクリル酸とメタクリル酸との共重合体
のアルカリ中和物からなる水ゲルによる方法が提案(特
開昭48−079951参照)されている。In addition, as a method for delaying the vaporization of the injected water by radiant heat to prevent the spread of fire, it is composed of an alkali neutralized product of water and an acrylic acid polymer or a copolymer of water, acrylic acid and methacrylic acid. A method using a water gel has been proposed (see JP-A-48-079951).
この水ゲルによる方法においては、建物等の外壁や天井
面に付着させることは容易にできるが、放射熱を受けて
水ゲルの温度が上昇すると粘度が下がり、ガラス等の表
面が滑らかな垂直面にゲル層を形成させようとしても、
滑り落ちてしまうため、延焼抑制の面で十分なゲル層を
形成させることが困難な状況であった。In this water gel method, it can be easily attached to the outer wall or ceiling surface of a building, etc., but when the temperature of the water gel rises due to radiant heat, the viscosity decreases, and the surface of glass, etc. is a smooth vertical surface. Even if you try to form a gel layer on
Since it slips off, it has been difficult to form a gel layer sufficient in terms of suppressing the spread of fire.
(発明が解決しようとする問題点) 上記注水による延焼抑制方法は、水の冷却作用によるも
のであるが、水は流動性が高いため、注水量に比較して
付着量が少なく、放射熱を受けるとすぐに気化してしま
うため、断続的または継続的に注水する必要がある。(Problems to be Solved by the Invention) The method for suppressing the spread of fire by pouring water is based on the cooling action of water, but since water has high fluidity, the amount of adhesion is small compared to the amount of pouring water and radiant heat is not generated. Since it vaporizes immediately after receiving it, it is necessary to inject water intermittently or continuously.
また、放射熱による気化を遅延させ、冷却による延焼抑
制効果を持続させるためには、水をゲル化させてゲル層
を形成させる方法があるが、建物火災の場合、ガラス等
の表面が滑らかな垂直面にも容易にゲル層を形成でき、
さらに、高温度の放射熱を受けても、容易に脱落しない
ゲル層を形成させることが必要である。In addition, in order to delay the vaporization by radiant heat and maintain the effect of suppressing the spread of fire by cooling, there is a method of gelating water to form a gel layer, but in the case of a building fire, the surface of glass etc. is smooth. A gel layer can be easily formed on a vertical surface,
Furthermore, it is necessary to form a gel layer that does not easily fall off even when it receives radiant heat at a high temperature.
(問題点を解決するための手段) 本発明は、火災時における上記の問題点を解決するた
め、付着性に優れ受熱によって熱ゲル化する性状を有す
る、粉粒体のヒドロキシプロピルメチルセルロース、ヒ
ドロキシエチルメチルセルロース等の非イオン性の水溶
性セルロースエーテル等に粉粒体のアクリル酸重合物ナ
トリウム塩、デンプン−アクリル酸グラフト共重合体等
の高吸水性樹脂を添加混合したもので、その目的とする
ところは、粉粒体のヒドロキシプロピルメチルセルロー
ス、ヒドロキシエチルメチルセルロース等の非イオン性
の水溶性セルロースエーテルを主体として吸水させた場
合、放射熱を受けない常温の状態では流動性のあるゾル
状であり、ゲル層を形成させることができない。(Means for Solving Problems) In order to solve the above problems at the time of a fire, the present invention has a property of being excellent in adhesiveness and having a property of being thermally gelated by receiving heat, hydroxypropylmethylcellulose, hydroxyethyl in the form of powder or granules. A nonionic water-soluble cellulose ether such as methyl cellulose and the like, which are added and mixed with a super absorbent polymer such as sodium salt of acrylic acid polymer in the form of granules, starch-acrylic acid graft copolymer, and the like. Is a fluid sol at room temperature that does not receive radiant heat when water is mainly absorbed by nonionic water-soluble cellulose ethers such as powdered hydroxypropylmethylcellulose and hydroxyethylmethylcellulose. No layers can be formed.
そこで、放射熱を受けない常温の状態においても、前記
記載の非イオン性の水溶性セルロースエーテル等をその
場合に留め、かつ、火災等の燃焼物からの放射熱を受け
る前においても、ゲル層を形成させるための手段とし
て、吸水・保水能力の高いアクリル酸重合物ナトリウム
塩、デンプン−アクリル酸グラフト共重合体等の高吸水
性樹脂を添加したものである。Therefore, even in a room temperature state where radiant heat is not received, the nonionic water-soluble cellulose ether or the like described above is retained in that case, and even before receiving radiant heat from a combustion product such as a fire, the gel layer As a means for forming the polymer, a highly water-absorbent resin such as sodium salt of acrylic acid polymer having high water absorption / water retention ability and starch-acrylic acid graft copolymer is added.
このような目的から構成された薬剤を用いて生成された
ゲルは、常温においてもガラス等の表面が滑らかな垂直
面へも容易にゲル層を形成でき、さらに、このゲル層が
放射熱を受けると、ゲル内に含有されている非イオン性
の水溶性セルロースエーテル等が熱ゲル化し、より強固
なゲル層が形成され、放射熱の影響によるゲル層の脱落
等を遅延させる効果を有しているため、高吸水性樹脂を
主体としたゲルと比較して、延焼抑制効果を持続させる
ことが可能となる。A gel produced using a drug configured for such a purpose can easily form a gel layer on a vertical surface having a smooth surface such as glass even at room temperature, and the gel layer receives radiant heat. And, the nonionic water-soluble cellulose ether contained in the gel is thermally gelled to form a stronger gel layer, which has the effect of delaying the falling of the gel layer due to the effect of radiant heat. Therefore, it is possible to maintain the effect of suppressing the spread of fire as compared with a gel containing a super absorbent polymer as a main component.
本発明における粉粒体の非イオン性の水溶性セルロース
エーテル等の条件としては、吸水後に受熱した場合、容
易に熱分解せず熱ゲル化し、付着性を損なわないこと、
さらに、水に速く均一に溶解することがあげられる。The conditions such as the nonionic water-soluble cellulose ether of the granular material in the present invention, when receiving heat after absorbing water, thermal gelation without thermal decomposition easily, not to impair the adhesiveness,
Further, it can be dissolved in water quickly and uniformly.
また、この粉粒体の非イオン性の水溶性セルロースエー
テル等に添加混合する高吸水性樹脂の条件としては、多
量の水を速く吸水し、吸水した水を離さない保水性のよ
いこと、付着性が高いこと及び取扱上人体に毒性の無い
ことがあげられる。Further, the condition of the superabsorbent resin to be added to and mixed with the nonionic water-soluble cellulose ether or the like of this granular material is that it absorbs a large amount of water quickly, does not separate the absorbed water, and has good water retention. It is highly effective and has no toxicity to the human body in handling.
これらの条件を満たした、非イオン性の水溶性セルロー
スエーテル等と高吸水性樹脂からなる延焼抑制剤を、水
と混合させ生成されたゲルは、高粘性かつ付着性に優れ
ており、さらに、受熱によって熱ゲル化するため、高吸
水性樹脂のみで生成したゲルと異なり、ガラス等の表面
が滑らかな垂直面へ容易に遮熱効果の高いゲル層を形成
することができ、燃焼物からの接炎、または放射熱を受
けても熱ゲル化によって、遮熱効果が持続するため、従
来のように受熱面に断続的または継続的な注水を行って
冷却しなくても、延焼を抑制する効果が得られる。Satisfying these conditions, a non-ionic water-soluble cellulose ether or the like and a fire spread inhibitor consisting of a superabsorbent resin, a gel produced by mixing with water is highly viscous and excellent in adhesiveness, Since it heat-gelates by receiving heat, unlike a gel produced only with superabsorbent resin, it is possible to easily form a gel layer with a high heat-shielding effect on a vertical surface where the surface of glass etc. is smooth. Even if it receives flame contact or radiant heat, the heat-shielding effect will continue due to thermal gelation, so the spread of heat will be suppressed even if cooling is not performed by intermittent or continuous water injection on the heat-receiving surface as in the past. The effect is obtained.
(実施例) この延焼抑制剤を用いて生成されたゲル層の熱ゲル化状
況、及び遮熱効果を確認するため、上記の非イオン性の
水溶性セルロースエーテル等として、化学名:ヒドロキ
シプロピルメチルセルロース、品名:ハイ・メトローズ
〔信越化学工業株式会社製〕、これに添加混合させる高
吸水性樹脂として、組成:アクリル酸重合物ナトリウム
塩、品名:スミカゲルN−100〔住友化学工業株式会
社製〕を用いて、下記の割合で水と混合させ生成した、
ゲルの延焼抑制効果に関する実施例を説明する。(Example) In order to confirm the thermal gelation state of the gel layer produced by using this fire spread inhibitor, and the heat shield effect, the chemical name: hydroxypropylmethylcellulose was used as the above nonionic water-soluble cellulose ether. Product name: Hi-Metroze (manufactured by Shin-Etsu Chemical Co., Ltd.), as superabsorbent resin to be added and mixed with it, composition: acrylic acid polymer sodium salt, product name: Sumikagel N-100 (manufactured by Sumitomo Chemical Co., Ltd.) It was produced by mixing with water in the following proportions,
An example of the effect of suppressing the spread of the gel will be described.
(重量%) ハイ・メトローズ 0.5 スミカゲルN−100 0.5 水 99.0 上記組成のゲルを生成し、合板及び普通板ガラスに平均
0.5cmの厚さに付着させたものと、1分間注水したも
のを試験体として用い、両試験体に受熱させた場合の遮
熱効果の相違を調べた。(% By weight) High Metroze 0.5 Sumikagel N-100 0.5 Water 99.0 A gel having the above composition was produced and adhered to plywood and ordinary plate glass to a thickness of 0.5 cm on average for 1 minute. The water-poured sample was used as a test body, and the difference in the heat-shielding effect when heat was applied to both test bodies was examined.
実験方法は、第1図に示す加熱試験炉を用いて、その前
面に試験体を置き、合板においては受熱面の表面温度、
普通板ガラスにおいては裏面温度を計測するとともに、
その状況変化を観測した。The experimental method is as follows. The heating test furnace shown in FIG. 1 is used, a test piece is placed on the front surface, and the surface temperature of the heat receiving surface in plywood,
For ordinary flat glass, while measuring the backside temperature,
The situation change was observed.
なお、加熱試験炉にあっては、建築用防火戸の防火試験
方法(JIS A1311−1975)に定める炉を用
い、炉面温度をほぼ800℃になるように設定した。As the heating test furnace, a furnace specified by the fireproof test method for building fire doors (JIS A1311-1975) was used, and the furnace surface temperature was set to approximately 800 ° C.
合板の実験では、第2図に示すように1分間注水した合
板と、高粘性かつ付着性の高いゲル層を形成させた合板
の表面温度上昇変化を比較した場合、高粘性かつ付着性
の高いゲル層を形成させた合板は、1分間注水した合板
に比べ、温度上昇が緩やかであった。In the experiment of plywood, as shown in Fig. 2, when comparing the change in the surface temperature of plywood that has been injected with water for 1 minute and the plywood that has formed a gel layer with high viscosity and high adhesiveness, it has high viscosity and high adhesiveness. The temperature rise of the plywood on which the gel layer was formed was slower than that of the plywood that was filled with water for 1 minute.
1分間注水した合板では、加熱してから8分過ぎに50
0℃に達し、試験体全面が黒色になった。しかしなが
ら、高粘性かつ付着性の高いゲル層を形成させた合板の
表面温度は、10分経過後も70℃であり、この時点の
高粘性かつ付着性の高いゲル層の状態は、非イオン性の
水溶性セルロースエーテル等が熱ゲル化し、白濁してい
るのが確認された。For plywood that has been infused with water for 1 minute, 50 minutes after 8 minutes from heating
The temperature reached 0 ° C., and the entire surface of the test body became black. However, the surface temperature of the plywood on which the highly viscous and highly adherent gel layer was formed was 70 ° C. even after 10 minutes, and the state of the highly viscous and highly adherent gel layer at this point was nonionic. It was confirmed that the water-soluble cellulose ether and the like of (1) became a heat gel and became cloudy.
実験後のゲル層の下の合板表面の状態は、実験開始前の
状態と変わらなかった。The state of the plywood surface under the gel layer after the experiment was the same as the state before the start of the experiment.
さらに、普通板ガラスの実験では、第3図に示すよう
に、1分間注水した普通板ガラスと、高粘性かつ付着性
の高いゲル層を形成させた普通板ガラスの裏面温度変化
を比較した。Further, in the experiment of the ordinary plate glass, as shown in FIG. 3, the backside temperature change between the ordinary plate glass which was poured with water for 1 minute and the ordinary plate glass on which a gel layer having high viscosity and high adhesiveness was formed was compared.
この実験における結果としては、高粘性かつ付着性の高
いゲル層を形成させた普通板ガラスは、1分間注水した
普通板ガラスに比べ温度上昇が緩やかであった。As a result of this experiment, the temperature of the ordinary plate glass on which the gel layer having high viscosity and high adhesiveness was formed was slower than that of the ordinary plate glass which was water-poured for 1 minute.
また、1分間注水した普通板ガラスの方は、加熱してか
ら3分後に200℃に達し、亀裂が入り部分的に落下し
た。In addition, the ordinary flat glass that had been water-poured for 1 minute reached 200 ° C. 3 minutes after heating and cracked and partially dropped.
一方、高粘性かつ付着性の高いゲル層を形成させた普通
板ガラスは、加熱してから6分後まで実験開始前の状態
と変わらなかった。On the other hand, the ordinary plate glass on which the highly viscous and highly adherent gel layer was formed did not change from the state before the start of the experiment until 6 minutes after heating.
この高粘性かつ付着性の高いゲルに添加されている、ハ
イ・メトローズの熱ゲル化温度は、本実験では、60〜
70℃前後の温度が最適であるという結果が得られた
が、炉面温度がほぼ800℃という悪条件にもかかわら
ず、高吸水性樹脂によって保水している水の気化によ
り、実験開始から10分後においても、ゲル層内の温度
は70℃を保っており、この結果においても高吸水性樹
脂の持つ保水性と、非イオン性の水溶性セルロースエー
テル等の熱ゲル化の相乗効果により、長時間の遮熱効果
が得られた。In the present experiment, the thermal gelation temperature of High-Metroze added to this highly viscous and highly adherent gel is 60-
The optimum temperature was about 70 ° C. However, despite the bad condition that the furnace surface temperature was about 800 ° C, the evaporation of the water retained by the superabsorbent resin caused 10 Even after the minute, the temperature in the gel layer was kept at 70 ° C. Even in this result, due to the synergistic effect of the water retention of the highly water-absorbent resin and the thermal gelation of the nonionic water-soluble cellulose ether, A long-term heat shield effect was obtained.
この一連の実験結果から、本延焼抑制剤を用いて生成し
た、高粘性かつ付着性の高いゲルを、燃焼物からの接炎
及び輻射熱の影響を受け、延焼するおそれのある物体に
付着させた場合、従来の注水による延焼抑制方法と比較
し、顕著な延焼抑制効果があることが確認された。From the results of this series of experiments, a highly viscous and highly adherent gel produced using the main flame retardant was adhered to an object that is susceptible to flame spread under the influence of flame contact and radiant heat from combustion products. In this case, it was confirmed that there was a remarkable effect of suppressing the spread of fire as compared with the conventional method of suppressing the spread of fire.
(発明の効果) 本発明は、以上述べたように延焼抑制剤を用いて生成し
たゲルは、高粘性かつ付着性が高く、ガラス等の表面が
滑らかな垂直面にも容易にゲル層を形成させることがで
き、さらに、受熱によっても熱ゲル化し、遮熱効果が持
続され、延焼を抑制することができる。(Effect of the invention) As described above, according to the present invention, the gel produced by using the flame retardant has a high viscosity and a high adhesive property, and easily forms a gel layer even on a vertical surface having a smooth surface such as glass. In addition, heat gelation occurs even when heat is received, the heat shield effect is maintained, and fire spread can be suppressed.
したがって、火災時に延焼を抑制するための消防活動に
おいて、本発明の延焼抑制剤を用いて、延焼危険の大き
い部分へ使用すれば、従来の注水による延焼抑制方法と
比べ、少ない水量で有効な延焼抑制効果をあげることが
できる特徴を有するものである。Therefore, in a fire fighting activity for suppressing the spread of fire during a fire, if the spread inhibiting agent of the present invention is used for a portion with a high risk of spread of fire, compared to the conventional method of suppressing the spread of fire by water injection, an effective spread of fire is achieved with a small amount of water. It has a feature that the suppression effect can be enhanced.
第1図は、本発明の延焼抑制剤の効果を確認するための
実験方法の概要を示す。 第2図は、合板を加熱試験炉の前において測定した、表
面温度変化及び炉面温度変化を示す。 第3図は、普通板ガラスを加熱試験炉の前に置いて測定
した、裏面温度変化及び炉面温度変化を示す。 1……加熱試験炉、2……試験体(合板50cm×30cm
×3mm)、普通板ガラス70cm×30cm×3mm)、3…
…加熱試験炉前面から試験体までの距離60cm、4……
炉面温度変化、5……1分間注水した合板の温度変化、
6……高粘性かつ付着性の高いゲルを付着させた合板の
温度変化、7……炉面温度変化、8……1分間注水した
普通板ガラスの温度変化、9……高粘性かつ付着性の高
いゲルを付着させた普通板ガラスの温度変化。FIG. 1 shows an outline of an experimental method for confirming the effect of the fire spread inhibitor of the present invention. FIG. 2 shows the surface temperature change and the furnace surface temperature change of the plywood measured in front of the heating test furnace. FIG. 3 shows the back surface temperature change and the furnace surface temperature change measured by placing the ordinary plate glass in front of the heating test furnace. 1 ... Heating test furnace, 2 ... Test body (plywood 50 cm x 30 cm
× 3mm), ordinary plate glass 70cm × 30cm × 3mm), 3 ...
… Distance from the front of the heating test furnace to the test piece 60 cm, 4 ……
Temperature change of furnace surface, 5 ... Temperature change of plywood poured with water for 1 minute,
6 …… Change in temperature of plywood with highly viscous and highly adherent gel attached, 7 …… Change in surface temperature of furnace, 8 …… Change in temperature of ordinary plate glass poured with water for 1 minute, 9 …… High viscous and adherent Temperature change of ordinary flat glass with high gel attached.
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭56−157479(JP,A) 特開 昭56−49167(JP,A) ─────────────────────────────────────────────────── --Continued from the front page (56) References JP-A-56-157479 (JP, A) JP-A-56-49167 (JP, A)
Claims (1)
ース、ヒドロキシエチルメチルセルロース等の非イオン
性の水溶性セルロースエーテル等に粉粒体のアクリル酸
重合物ナトリウム塩、デンプン−アクリル酸グラフト共
重合体等の高吸水性樹脂を添加混合させた薬剤で、これ
に吸水させ生成されたゲルは、火災等の放射熱を受ける
と、受熱によってヒドロキシプロピルメチルセルロー
ス、ヒドロキシエチルメチルセルロース等の非イオン性
の水溶性セルロースエーテル等が熱ゲル化し、より強固
なゲル層を形成させることができることを特徴とする延
焼抑制剤。Claims: 1. Nonionic water-soluble cellulose ethers such as hydroxypropylmethylcellulose and hydroxyethylmethylcellulose in the form of powder and granular acrylic acid polymer sodium salt, starch-acrylic acid graft copolymer and the like A water-absorbent resin is added and mixed, and the resulting gel absorbs water, and when it receives radiant heat from a fire, etc., it receives non-ionic water-soluble cellulose ethers such as hydroxypropylmethylcellulose and hydroxyethylmethylcellulose. Is a heat-gelable product, which can form a stronger gel layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62211304A JPH0626622B2 (en) | 1987-08-27 | 1987-08-27 | Fire spread inhibitor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62211304A JPH0626622B2 (en) | 1987-08-27 | 1987-08-27 | Fire spread inhibitor |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6456070A JPS6456070A (en) | 1989-03-02 |
JPH0626622B2 true JPH0626622B2 (en) | 1994-04-13 |
Family
ID=16603726
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62211304A Expired - Lifetime JPH0626622B2 (en) | 1987-08-27 | 1987-08-27 | Fire spread inhibitor |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0626622B2 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2778878B2 (en) * | 1991-09-12 | 1998-07-23 | 株式会社日本触媒 | Method for producing ethylene oxide |
US20030038272A1 (en) | 2001-08-24 | 2003-02-27 | Figiel Edmund W. | Fire retardant foam and gel compositions |
JP2014230579A (en) * | 2013-05-28 | 2014-12-11 | 信越化学工業株式会社 | Aqueous solution of fire spreading inhibitor |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5649167A (en) * | 1979-09-26 | 1981-05-02 | Miyata Ind | Fireeextinguishing substanse |
JPS56157479A (en) * | 1980-04-10 | 1981-12-04 | Jiyon Enu Shiyuwaatsuman | Water-barrier gel synthetic matter and fireproofing method |
-
1987
- 1987-08-27 JP JP62211304A patent/JPH0626622B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPS6456070A (en) | 1989-03-02 |
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