JPS6216654B2 - - Google Patents
Info
- Publication number
- JPS6216654B2 JPS6216654B2 JP52138473A JP13847377A JPS6216654B2 JP S6216654 B2 JPS6216654 B2 JP S6216654B2 JP 52138473 A JP52138473 A JP 52138473A JP 13847377 A JP13847377 A JP 13847377A JP S6216654 B2 JPS6216654 B2 JP S6216654B2
- Authority
- JP
- Japan
- Prior art keywords
- fire extinguishing
- foam
- surfactant
- silica
- weight
- 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
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 61
- 239000006260 foam Substances 0.000 claims description 44
- 239000000377 silicon dioxide Substances 0.000 claims description 25
- 239000004094 surface-active agent Substances 0.000 claims description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 18
- 239000000843 powder Substances 0.000 claims description 15
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims description 14
- 235000012239 silicon dioxide Nutrition 0.000 claims description 14
- 239000002245 particle Substances 0.000 claims description 13
- 150000008282 halocarbons Chemical class 0.000 claims description 10
- 238000002156 mixing Methods 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 4
- 238000005187 foaming Methods 0.000 description 22
- 239000006185 dispersion Substances 0.000 description 11
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 7
- 229910002016 Aerosil® 200 Inorganic materials 0.000 description 6
- 239000003945 anionic surfactant Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- JLGADZLAECENGR-UHFFFAOYSA-N 1,1-dibromo-1,2,2,2-tetrafluoroethane Chemical compound FC(F)(F)C(F)(Br)Br JLGADZLAECENGR-UHFFFAOYSA-N 0.000 description 2
- 229910002012 Aerosil® Inorganic materials 0.000 description 2
- -1 Polyoxyethylene Polymers 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 239000011882 ultra-fine particle Substances 0.000 description 2
- RNMDNPCBIKJCQP-UHFFFAOYSA-N 5-nonyl-7-oxabicyclo[4.1.0]hepta-1,3,5-trien-2-ol Chemical compound C(CCCCCCCC)C1=C2C(=C(C=C1)O)O2 RNMDNPCBIKJCQP-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- LRMHFDNWKCSEQU-UHFFFAOYSA-N ethoxyethane;phenol Chemical compound CCOCC.OC1=CC=CC=C1 LRMHFDNWKCSEQU-UHFFFAOYSA-N 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Description
本発明は泡消火剤に関し、詳言すれば水と界面
活性剤とから成る界面活性剤系泡消火剤の改良に
関する。
一般に、ガソリン、重油等の大規模な油火災に
対しては蛋白系泡消火剤が用いられているが、こ
の泡消火剤は原液貯蔵安定性や起泡性等があまり
良くない。
そこで、この蛋白系泡消火剤の欠点を改善する
ために合成界面活性剤系(以下単に界面活性剤系
という)泡消火剤が開発された。ところが、この
界面活性剤系泡消火剤は原液貯蔵安定性、起泡性
等は良好であるものの水と界面活性剤とから成る
ために耐熱性に劣り、このため消火能力が不十分
であり広く使用されるまでには至つていない。
上述の如き実情に鑑み、本発明は界面活性剤系
泡消火剤の耐熱性を向上すべく種々研究の結果完
成したものであり、その構成は、粒子径が50mμ
以下の極微粒子状のシリカ、界面活性剤及び水を
混合して成ることを特徴とし、更に粒子径が50m
μ以下の極微粒子状のシリカ、ハロゲン化炭化水
素、界面活性剤及び水を混合してなることを特徴
とする。
本発明に係る泡消火剤を実施例を参照して以下
詳細に説明する。先づ、本発明に係る第1の泡消
火剤は粒子径が50mμ以下の極微粒子状のシリカ
と界面活性剤を水と混合して成る。シリカは成可
く粒度の小さいものを用いるものが望ましく、通
常は無水ケイ酸粉末又は含水ケイ酸粉末を用いる
のが適当である。配合量は0.1wt%以上とするの
が良いが、10wt%以上としてもそれほど消火能
力が増大しないので通常は0.1〜10wt%が適当で
あり、好ましくは0.5〜5wt%とする。また、界面
活性剤は従来の界面活性剤系泡消火剤に使用され
ていたものを用いて良く、アニオン系、両性イオ
ン系、ノニオン系の何れを用いても良い。配合量
も従来の泡消火剤の場合と同等で良く、即ち1〜
10wt%好ましくは2〜6wt%とする。更に、各成
分を混合する場合極微粒子状のシリカは水に離溶
性であるから予め適当量の水と混合して水分散液
を調製し、このシリカの水分散液に界面活性剤を
必要に応じ溶液として混合するようにすると良
い。
上記泡消火剤は従来の泡消火剤に比べて消火能
力が優れ、消火所要時間が短かく、且つ再着火時
間が長い。この理由は明らかではないが、シリカ
が極微粒子状であるために発泡時泡膜中にシリカ
が分散して保持されることにより泡が補強される
ためであると推測される。
次に、上記の第1の泡消火剤にハロゲン化炭化
水素を配合すると更に消火能力が増大する。即
ち、この本発明に係る第2の泡消火剤は極粒子状
のシリカ、ハロゲン化炭化水素、界面活性剤及び
水を混合して成り、消火所要時間が著しく短縮さ
れる。シリカ及び界面活性剤は第1の泡消火剤の
場合と同様のものを用い、ハロゲン化炭化水素は
種々のものが使用可能であるが通常はC2Br2F4、
CBrF3、CBrClF2などを用いると良い。配合量
は、シリカが0.5〜10wt%、好ましくは1〜5wt
%、界面活性剤が1〜10wt%好ましくは3〜8wt
%、ハロゲン化炭化水素は0.5乃至数+wt%、好
ましくは0.5〜10wt%とするのが良い。更に、各
成分を混合する場合は前述した様に予めシリカの
水分散液を調製しておくと良く、また使用する場
合は発泡用ノズルから放出するが、この場合予め
混合したものをノズルへ送給しても或いは配管中
に乱流等を起こして輸送中に混合したりノズル内
で混合したりしても良い。また、通常は空気を用
いて発泡させるが、気体状のハロゲン化炭化水素
を使用する場合はこのハロゲン化炭化水素により
発泡させても良い。
次に実施例を挙げて本発明を更に詳細に説明す
る。なお、各測定値は特に記さない限り次の様に
して測定した。
(i) 発泡倍率
泡消火剤を流量3/min、放出圧5Kg/cm2で
発泡用ノズルから放出したときの発泡倍率を測定
する。
(ii) 消火所要時間
77.5cm×77.5cm×30cmのオイルピツトに水を深
さ12cm、ガソリンを深さ3cmになるよう注入して
点火し、1分間経過後泡消火剤を流量3/
min、放出圧5Kg/cm2で発泡用ノズルから発泡さ
せて一定個所に放出し消火するまでに要する時間
を測定する。
(iii) 再着火時間
27cm×33cm×14cmのオイルピツトに水を深さ4
cm、n―ヘプタンを深さ3cmになるよう注入する
一方該オイルピツトの中央部に直径54mm、高さ
100mm、厚み3.5mmのステンレスパイプを直立させ
て該ステンレスパイプの外側のn―ベプタンに点
火し、1分間経過後泡消火剤を流量3/min、
放出圧5Kg/cm2で発泡用ノズルから発泡させて放
出し消火する。次に、消火から3分後ステンレス
パイプ内の泡消火剤を除去して点火し、この点火
時からパイプ外側のn―ヘプタンに再着火するま
での時間を測定する。
<実施例 1>
極微粒子状シリカとして無水ケイ酸粉末又は含
水ケイ酸粉末を用い、これらの水分散液にアニオ
ン系界面活性剤を加え混合して種々の組成の泡消
火剤を調製しその発泡倍率、消火所要時間及び再
着火時間を測定する。無水ケイ酸粉末は日本アエ
ロジル株式会社製の商品名アエロジル―200(粒
子径12mμ、比表面積200m2/g)、含水ケイ酸粉
末は日本シリカ工業株式会社製の商品名ニプシル
ーLP(粒子径16mμ、比表面積230m2/g)、界
面活性剤は東邦化学株式会社製の商品名アルスコ
ープLE―213を夫々使用した。なお、比較例とし
て極微粒子状シリカを配合しないもの、或いはシ
リカとして粒子径の大きい沈降シリカ(粒子径57
μ、比表面積510m2/g)又は粉砕シリカ(粒子
径12μ、比表面積2300cm2/g)を使用したものに
ついても測定した。結果を第1表に示す。
第1表の結果から、本発明に係る泡消火剤はシ
リカを含まないもの、或いは粗粒子状シリカを含
むものに比べて非常に消火能力が優れていること
が判り、また、無水ケイ酸粉末を用いた場合は、
2wt%、含水ケイ酸粉末を用いた場合は5wt%ま
で著しく消火能力が増大しそれ以上の配合量にす
ると徐々に増大することが判る。なお本実施例で
は極微粒子状シリカとしてアエロジル―200又は
ニプシル―LP、界面活性剤としてアルスコープ
LE―213を用いたが、
The present invention relates to fire extinguishing foam, and more specifically to improvements in surfactant-based fire extinguishing foam consisting of water and a surfactant. Generally, protein-based fire extinguishing foam is used for large-scale oil fires caused by gasoline, heavy oil, etc., but this foam fire extinguishing agent does not have very good stock solution storage stability or foaming properties. Therefore, in order to improve the drawbacks of this protein-based fire extinguishing foam, a synthetic surfactant-based (hereinafter simply referred to as surfactant-based) foam fire extinguishing agent was developed. However, although this surfactant-based fire extinguishing foam has good stock stability and foaming properties, it has poor heat resistance because it is composed of water and a surfactant, and therefore has insufficient fire extinguishing ability and is not widely used. It has not yet been used. In view of the above-mentioned circumstances, the present invention was completed as a result of various studies to improve the heat resistance of surfactant-based fire extinguishing foam.
It is characterized by being made by mixing the following ultrafine particulate silica, surfactant and water, and further has a particle size of 50m.
It is characterized by being made by mixing silica in the form of ultrafine particles of micron size or less, a halogenated hydrocarbon, a surfactant, and water. The fire extinguishing foam according to the present invention will be described in detail below with reference to Examples. First, the first fire extinguishing foam according to the present invention is made by mixing ultrafine silica particles with a particle size of 50 mμ or less and a surfactant with water. It is desirable to use silica that can be easily formed and has a small particle size, and it is usually appropriate to use anhydrous silicic acid powder or hydrated silicic acid powder. The blending amount is preferably 0.1 wt% or more, but even if it is 10 wt% or more, the fire extinguishing ability will not increase significantly, so 0.1 to 10 wt% is usually appropriate, and preferably 0.5 to 5 wt%. Moreover, the surfactant used in conventional surfactant-based fire extinguishing foams may be used, and any of anionic, amphoteric, and nonionic surfactants may be used. The blending amount may be the same as that for conventional fire extinguishing foam, i.e. 1 to
10 wt%, preferably 2 to 6 wt%. Furthermore, when mixing each component, since ultrafine silica is dissolvable in water, it is necessary to mix it with an appropriate amount of water in advance to prepare an aqueous dispersion, and add a surfactant to this aqueous silica dispersion. It is best to mix it as a solution. The above foam fire extinguishing agent has superior fire extinguishing ability compared to conventional foam fire extinguishing agents, requires a shorter extinguishing time, and has a longer re-ignition time. Although the reason for this is not clear, it is presumed that since silica is in the form of ultrafine particles, the silica is dispersed and retained in the foam membrane during foaming, thereby reinforcing the foam. Next, when a halogenated hydrocarbon is added to the first fire extinguishing foam, the fire extinguishing ability is further increased. That is, the second fire extinguishing foam according to the present invention is a mixture of extremely particulate silica, a halogenated hydrocarbon, a surfactant, and water, and the time required for fire extinguishing is significantly shortened. The same silica and surfactant as in the first fire extinguishing foam are used, and various halogenated hydrocarbons can be used, but usually C 2 B r2 F 4 ,
It is preferable to use CB r F 3 , CB r ClF 2 , etc. The blending amount is 0.5 to 10 wt% silica, preferably 1 to 5 wt%.
%, surfactant is 1-10wt%, preferably 3-8wt%
%, and the halogenated hydrocarbon is 0.5 to several + wt%, preferably 0.5 to 10 wt%. Furthermore, when mixing each component, it is best to prepare an aqueous dispersion of silica in advance as described above, and when using it, it is discharged from a foaming nozzle, but in this case, the pre-mixed silica is sent to the nozzle. Alternatively, they may be mixed during transportation by creating turbulent flow in piping, or may be mixed within a nozzle. Further, although air is usually used for foaming, if a gaseous halogenated hydrocarbon is used, the halogenated hydrocarbon may be used for foaming. Next, the present invention will be explained in more detail with reference to Examples. In addition, each measurement value was measured as follows unless otherwise noted. (i) Foaming ratio Measure the foaming ratio when the fire extinguishing foam is discharged from the foaming nozzle at a flow rate of 3/min and a discharge pressure of 5Kg/cm 2 . (ii) Time required for fire extinguishing Pour water to a depth of 12 cm and gasoline to a depth of 3 cm into an oil pit measuring 77.5 cm x 77.5 cm x 30 cm, ignite it, and after 1 minute, pour fire extinguishing foam at a flow rate of 3/3 cm.
Foam is generated from a foaming nozzle at a discharge pressure of 5 kg/cm 2 , and the time required to extinguish the fire is measured. (iii) Re-ignition time: Pour water into a 27cm x 33cm x 14cm oil pit to a depth of 4.
cm, n-heptane to a depth of 3 cm, and a diameter of 54 mm and a height of 54 mm to the center of the oil pit.
A stainless steel pipe of 100mm and 3.5mm thickness is stood upright, and the n-beptane outside the stainless steel pipe is ignited, and after 1 minute, fire extinguishing foam is applied at a flow rate of 3/min.
Foam is discharged from the foaming nozzle at a discharge pressure of 5 kg/cm 2 to extinguish the fire. Next, 3 minutes after extinguishing the fire, the foam extinguishing agent inside the stainless steel pipe is removed and ignited, and the time from the time of ignition until the n-heptane outside the pipe is re-ignited is measured. <Example 1> Using anhydrous silicic acid powder or hydrated silicic acid powder as ultrafine particulate silica, anionic surfactants were added and mixed to an aqueous dispersion of these to prepare fire extinguishing foams of various compositions, and the foaming was performed. Measure the magnification, extinguishing time and re-ignition time. The anhydrous silicic acid powder is manufactured by Nippon Aerosil Co., Ltd. under the trade name Aerosil-200 (particle size 12 mμ, specific surface area 200 m 2 /g), and the hydrated silicic acid powder is manufactured by Nippon Silica Kogyo Co., Ltd. under the trade name Nipsiru LP (particle size 16 mμ, Specific surface area: 230 m 2 /g), and the surfactant used was Alscope LE-213 (trade name, manufactured by Toho Chemical Co., Ltd.). Comparative examples include those that do not contain ultrafine particulate silica, or precipitated silica with a large particle size (particle size 57).
µ, specific surface area 510 m 2 /g) or those using crushed silica (particle size 12 µ, specific surface area 2300 cm 2 /g) were also measured. The results are shown in Table 1. From the results in Table 1, it can be seen that the fire extinguishing foam according to the present invention has extremely superior fire extinguishing ability compared to those that do not contain silica or those that contain coarse particulate silica. If you use
It can be seen that the fire extinguishing ability increases significantly up to 2wt% and 5wt% when using hydrated silicic acid powder, and gradually increases when the amount is increased beyond that. In this example, Aerosil-200 or Nipsil-LP was used as the ultrafine particulate silica, and Arscope was used as the surfactant.
I used LE-213, but
【表】
粒子径50mμ以下の他の極微粒子状シリカや他の
界面活性剤を使用した場合も略同様な結果が得ら
れた。
<実施例 2>
実施例1で使用した無水ケイ酸粉末(アエロジ
ル―200)、含水ケイ酸粉末(ニプシル―LP)及
び界面活性剤(アルスコープLE―213)を用い、
更にハロゲン化炭化水素を配合して泡消火剤を調
製しその消火所要時間を測定した(第2表参
照)。なお、C2Br2F4を使用する場合は各成分の
混合分散液を発泡用ノズルから発泡させて放出
し、またCBrF3、CBrClF2の場合はシリカ及び界
面活性剤の混合分散液とCBrF3、CBrClF2とを
別々に発泡用ノズルから発泡室へ放出し、CBrF3
の場合は空気を導入せず、CBrClF2の場合は空気
を導入して発泡させた。
第2表の結果から、極微粒子状シリカとハロゲ
ン化炭化水素を配合すると消火所要時間が著しく
短縮されることが判る。[Table] Almost the same results were obtained when other ultrafine particulate silica with a particle size of 50 mμ or less and other surfactants were used. <Example 2> Using the anhydrous silicic acid powder (Aerosil-200), hydrated silicic acid powder (Nipsil-LP) and surfactant (Arscope LE-213) used in Example 1,
Furthermore, a halogenated hydrocarbon was blended to prepare a fire extinguishing foam, and the time required for extinguishing the foam was measured (see Table 2). In addition, when using C 2 B r 2 F 4 , the mixed dispersion of each component is foamed and discharged from a foaming nozzle, and when using CB r F 3 and CB r ClF 2 , silica and surfactant are mixed. The dispersion liquid, CB r F 3 and CB r ClF 2 are separately discharged from a foaming nozzle into a foaming chamber, and CB r F 3
In the case of CB r ClF 2 , air was introduced to cause foaming. From the results in Table 2, it can be seen that when ultrafine particulate silica and halogenated hydrocarbon are blended, the time required for extinguishing is significantly shortened.
【表】
<実施例 3>
実施例1で用いた粒子径12mμの極微粒子状無
水ケイ酸粉末(日本アエロジル株式会社製アエロ
ジルー200)2重量部と水95重量部から成る分散
液にポリオキシエチレンアルキルフエノールエー
テル硫酸ソーダ塩(アニオン系界面活性剤)を3
重量部加えて混合し泡消火剤を調製した。この泡
消火剤の発泡倍率は9倍、消火所要時間は50秒、
再着火時間は14分であつた。
<実施例 4>
実施例1で用いたアエロジル―200、2重量部
と水95重量部から成る分散液にポリオキシエチレ
ンノニルフエノールエーテル(ノニオン系界面活
性剤)3重量部を加えて混合し泡消火剤を調製し
た。この泡消火剤の発泡倍率は9倍、消火所要時
間は58秒、再着火時間は14分であつた。なお、本
実施例においては消火所要時間をガソリンの代り
にn―ヘプタンを用いて測定した。
<実施例 5>
実施例1で用いたアエロジル―200、2重量部
と水95重量部から成る分散液に日産化学工業株式
会社製の商品名スノーラツプ―H(アニオン系界
面活性剤)を3重量部加えて混合し泡消火剤を調
製した。この泡消火剤の発泡倍率は10倍、消火所
要時間は60秒、再着火時間は11分であつた。
<実施例 6>
実施例1で用いたアエロジル―200、2重量部
と水92重量部から成る分散液に実施例5で用いた
スノーラツプHを3重量部、ジブロモテトラフル
オロエタン(C2Br2F4)を3重量部加えて乳化分
散し泡消火剤を調製した。この泡消火剤の発泡倍
率は9倍、消火所要時間は28秒、再着火時間は10
分であつた。
<実施例 7>
実施例1で用いた粒子径16mμの極微粒子状含
水ケイ酸粉末(日本シリカ工業株式会社製ニプシ
ル―LP)3重量部と水94重量部から成る分散液
に三愛石油株式会社製の商品名スーパーフオーム
(アエオン系界面活性剤)を3重量部加えて混合
し泡消火剤を調製した。この泡消火剤の発泡倍率
は10倍、消火所要時間は62秒、再着火時間は10分
であつた。
<実施例 8>
実施例1で用いたニプシル―LP3重量部と水91
重量部から成る分散液に実施例7で用いたスーパ
ーフオームを3重量部、ジブロモテトラフルオロ
エタン(C2Br2F4)を3重量部加えて乳化分散し
泡消火剤を調製した。この泡消火剤の発泡倍率は
8倍、消火所要時間は30秒、再着火時間は11分で
あつた。[Table] <Example 3> Polyoxyethylene was added to a dispersion consisting of 2 parts by weight of ultrafine silicic anhydride powder with a particle size of 12 mμ (Aerogil 200 manufactured by Nippon Aerosil Co., Ltd.) used in Example 1 and 95 parts by weight of water. Alkyl phenol ether sulfate sodium salt (anionic surfactant)
Parts by weight were added and mixed to prepare a fire extinguishing foam. The foaming ratio of this fire extinguishing foam is 9 times, and the time required for extinguishing is 50 seconds.
Reignition time was 14 minutes. <Example 4> 3 parts by weight of polyoxyethylene nonylphenol ether (nonionic surfactant) was added to a dispersion of 2 parts by weight of Aerosil-200 used in Example 1 and 95 parts by weight of water, and the mixture was mixed to form foam. A fire extinguishing agent was prepared. The foaming ratio of this fire extinguishing foam was 9 times, the time required for extinguishing was 58 seconds, and the time for re-ignition was 14 minutes. In this example, the time required for extinguishing the fire was measured using n-heptane instead of gasoline. <Example 5> 3 weights of Snowrap-H (trade name, anionic surfactant) manufactured by Nissan Chemical Industries, Ltd. were added to a dispersion consisting of 2 parts by weight of Aerosil-200 used in Example 1 and 95 parts by weight of water. 1 part and mixed to prepare fire extinguishing foam. The foaming ratio of this fire extinguishing foam was 10 times, the time required for extinguishing was 60 seconds, and the time for re-ignition was 11 minutes. <Example 6> To a dispersion consisting of 2 parts by weight of Aerosil-200 used in Example 1 and 92 parts by weight of water, 3 parts by weight of Snowlap H used in Example 5 and dibromotetrafluoroethane (C 2 B r2 A fire extinguishing foam was prepared by adding 3 parts by weight of F 4 ) and emulsifying and dispersing it. The foaming ratio of this fire extinguishing agent is 9 times, the extinguishing time is 28 seconds, and the re-ignition time is 10 times.
It was hot in minutes. <Example 7> San-ai Oil Co., Ltd. was added to a dispersion consisting of 3 parts by weight of ultrafine hydrated silicic acid powder (Nipsil-LP manufactured by Nippon Silica Kogyo Co., Ltd.) with a particle size of 16 mμ used in Example 1 and 94 parts by weight of water. A fire extinguishing foam was prepared by adding and mixing 3 parts by weight of SUPERFOAM (Aeon-based surfactant) manufactured by KK. The foaming ratio of this fire extinguishing foam was 10 times, the time required for extinguishing was 62 seconds, and the time for re-ignition was 10 minutes. <Example 8> Nipsil-LP3 parts by weight used in Example 1 and 91 parts by weight of water
A fire extinguishing foam was prepared by adding 3 parts by weight of the superfoam used in Example 7 and 3 parts by weight of dibromotetrafluoroethane (C 2 B r2 F 4 ) to a dispersion consisting of parts by weight and emulsifying and dispersing them. The foaming ratio of this fire extinguishing foam was 8 times, the time required for extinguishing was 30 seconds, and the time for re-ignition was 11 minutes.
Claims (1)
界面活性剤及び水を混合してなる泡消火剤。 2 シリカが無水ケイ酸粉末又は含水ケイ酸粉末
である特許請求の範囲第1項記載の泡消火剤。 3 粒子径が50mμ以下の極微粒子状のシリカ、
ハロゲン化炭化水素、界面活性剤及び水を混合し
て成る泡消火剤。 4 シリカが無水ケイ酸粉末又は含水ケイ酸粉末
である特許請求の範囲第3項記載の泡消火剤。[Claims] 1. Ultrafine silica particles with a particle size of 50 mμ or less,
A fire extinguishing foam made by mixing a surfactant and water. 2. The fire extinguishing foam according to claim 1, wherein the silica is anhydrous silicic acid powder or hydrated silicic acid powder. 3 Ultrafine silica particles with a particle size of 50 mμ or less,
A fire extinguishing foam made of a mixture of halogenated hydrocarbon, surfactant and water. 4. The fire extinguishing foam according to claim 3, wherein the silica is anhydrous silicic acid powder or hydrated silicic acid powder.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13847377A JPS5471900A (en) | 1977-11-18 | 1977-11-18 | Foam fire-extinguishing agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13847377A JPS5471900A (en) | 1977-11-18 | 1977-11-18 | Foam fire-extinguishing agent |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5471900A JPS5471900A (en) | 1979-06-08 |
JPS6216654B2 true JPS6216654B2 (en) | 1987-04-14 |
Family
ID=15222872
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13847377A Granted JPS5471900A (en) | 1977-11-18 | 1977-11-18 | Foam fire-extinguishing agent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5471900A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5518638A (en) * | 1991-02-05 | 1996-05-21 | Buil; Jurgen | Fire extinguishing and protection agent |
US5607787A (en) * | 1993-05-04 | 1997-03-04 | Programme 3 Patent Holdings | High temperature storage battery |
DE102014005711A1 (en) * | 2014-04-22 | 2015-10-22 | Franz Wilhelm Cremer | Material preparations and devices for securing batteries and batteries during operation and transport, as well as during charging, storage and collection |
CN108096758A (en) * | 2017-12-06 | 2018-06-01 | 常州环际商贸有限公司 | A kind of protein foam extinguishing agent |
-
1977
- 1977-11-18 JP JP13847377A patent/JPS5471900A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5471900A (en) | 1979-06-08 |
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