JPS5829473A - Foam fire fighting agent - Google Patents

Foam fire fighting agent

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Publication number
JPS5829473A
JPS5829473A JP12907181A JP12907181A JPS5829473A JP S5829473 A JPS5829473 A JP S5829473A JP 12907181 A JP12907181 A JP 12907181A JP 12907181 A JP12907181 A JP 12907181A JP S5829473 A JPS5829473 A JP S5829473A
Authority
JP
Japan
Prior art keywords
water
fire extinguishing
extinguishing agent
foam
foam fire
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.)
Granted
Application number
JP12907181A
Other languages
Japanese (ja)
Other versions
JPS6019254B2 (en
Inventor
幸次 井上
高橋 良次
種山 洋一
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.)
JNC Corp
Original Assignee
Chisso Corp
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 Chisso Corp filed Critical Chisso Corp
Priority to JP12907181A priority Critical patent/JPS6019254B2/en
Publication of JPS5829473A publication Critical patent/JPS5829473A/en
Publication of JPS6019254B2 publication Critical patent/JPS6019254B2/en
Expired legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は木材などの一般火災(A火災)に対して極めて
鵡い消火能力を保持し低温及び高温においても、安定な
#l#I火薬剤(わしくは水成膜7形1m性能機械−消
火毫剤(以下總消火鵜剤ということがある)に関するも
のである。
Detailed Description of the Invention The present invention uses a #1 #I explosive (preferably aqueous This relates to membrane 7 type 1m performance machine fire extinguishing agent (hereinafter sometimes referred to as fire extinguishing agent).

近年、泡消火薬剤として泡沫拳威能力と共に餉mに水成
展形成能力を有するフッ素系界面活性剤を含有する組成
物の消火薬剤が開発され実用化されている。このフッ素
系界面活性剤は、フ身オhカルボンjllAヒフルオル
スルホン鐵の誘導体でC,F、、C00I(、C,F、
800Hの如自ものが使用されている。通常の巻金、市
販の水成膜泡消火薬剤(フッ素系界面活性剤)3容量チ
又は6容量−含有する水溶液として消火器に充填し使用
されていゐ。該水溶液は、消火Kllては、放射によp
池床の形成と共に油′FjiK水成捩を形成することに
より可燃性液体に対する消火能力は優れたものであるが
、水が主成分であるため一般火災に対する消火能力は劣
夛、凝固点も水の氷点に近いため寒冷地での使用は不可
能である・これに対して不aI液や消火効力のある化合
物などの各種添加剤を使用するのが常道の対策であるが
、この場合これらの添加剤を含めた組成物の安定性が極
めて重要となる。すなわち、添加剤により界面活性剤の
懸濁、分IIIToゐいは添加剤の影響による発泡性の
減少などがおこることなく性能及び水溶液としての安定
性が保持できることが必要である。消火器用消火薬剤と
して使用する場合、低温安定性と共に常温以上の高温で
の安定性に優れていることが%に重要である。夏期にお
ける屋外など40℃以上に加温されるようなことがしば
しばあるが、このような場合も懸濁、凝固、層分離の生
じない安定な組成物であることが必要である。
In recent years, fire extinguishing foam compositions have been developed and put into practical use as foam extinguishing agents, which contain a fluorine-based surfactant that has the ability to form water formation in addition to the ability to form foam. This fluorine-based surfactant is a derivative of fluorocarboxylic acid, C,F,,C00I(,C,F,
800H is used. It is used by filling a fire extinguisher as an aqueous solution containing 3 volumes or 6 volumes of a commercially available aqueous film-forming foam fire extinguishing agent (fluorosurfactant). The aqueous solution is extinguished by radiation.
It has excellent extinguishing ability against flammable liquids due to the formation of oil and water formation along with the formation of the pond bed, but since water is the main component, its extinguishing ability against general fires is poor, and its freezing point is also similar to that of water. It is impossible to use in cold regions because the temperature is close to the freezing point. ・The usual countermeasure for this is to use various additives such as anti-Al liquid and compounds with fire extinguishing effect, but in this case, these additives The stability of the composition, including the agent, is extremely important. That is, it is necessary that the performance and stability as an aqueous solution can be maintained without suspension of the surfactant caused by the additive, or a decrease in foaming properties due to the influence of the additive. When used as a fire extinguishing agent for fire extinguishers, it is important to have excellent stability at low temperatures as well as at high temperatures above room temperature. The composition is often heated to 40° C. or higher, such as outdoors in the summer, and even in such cases, it is necessary that the composition is stable and does not undergo suspension, coagulation, or layer separation.

以上の如く油火災(B火災という)に対して顕看1効力
を持つフッ素系昇−#1性剤の性能を保持しながら、A
火災に対しても動力が大で低温及び?#3龜にも安定な
泡消火薬剤が要望されているが、A火災に対す為消火総
力を大とし、凝固点が低く寒冷地で使用するものについ
てはすでに水系消火剤において樵々提案されている。
As mentioned above, A
Powerful enough to withstand fires and low temperatures? #3 There is a demand for a stable foam fire extinguishing agent for fires, but woodcutters have already proposed a water-based fire extinguishing agent that increases the total extinguishing force for A fires and has a low freezing point and can be used in cold regions. .

例えば■リン酸、アンモニア、モノエタノールアミンの
壇を用いてそのりン酸塩構成成分の七身比を調節するこ
とによシ、凝固点が一20℃以下で消火能力が3AA−
4のものが得られる(公開特許公報餡55−67995
入■硫酸アンモニウムと尿素、少量のリン酸3ナトリウ
ムにより凝固点−20℃51に−2の消火総力を有する
ものが得られる(公関特許公報昭52−56896)、
また、フッ素系界面活性剤を使用した消火電画に関して
も、■9ン酸モノエタノールアミンを使用し、凝固点−
20℃以下SL人−2の消火総力のものを得ることがで
きる(公開%杵公報昭55−14058  )、■硫酸
アンモニウム及び尿素、ポリビニールアルコールを用い
て凝固点−15t:以下、3tム−1のものを得ること
ができる(公lIl譬許公報@50−27598 )、
などが提案されている。
For example, by adjusting the ratio of the phosphate components using a mixture of phosphoric acid, ammonia, and monoethanolamine, the fire extinguishing ability can be increased to 3AA-3AA when the freezing point is below -20°C.
4 can be obtained (Publication Patent Publication No. 55-67995)
By using ammonium sulfate, urea, and a small amount of trisodium phosphate, a product having a freezing point of -20℃51 and a total extinguishing power of -2 can be obtained (Kokoku Patent Publication No. 56896/1989).
In addition, regarding fire extinguishing electrical painting using fluorine-based surfactants, we use
It is possible to obtain a total fire extinguishing force of 20℃ or less SL person-2 (Published % Pestle Bulletin Showa 55-14058), ■ Using ammonium sulfate, urea, and polyvinyl alcohol, freezing point -15t: Below, 3t μm-1 You can get things (public license publication @50-27598),
etc. have been proposed.

水系消火剤前記例について水成膜形成機械泡消火薬剤へ
の応用を試みるとフッ素系界面活性剤として市販の水成
膜泡消火薬剤を混合した場合は、常温でI!濁状態と彦
シ放置すると層分離をおこし使用不可能となった。又、
フッ素系界面活性剤を使用した消火薬剤として提案され
ている前記■、■の例の場合、フッ素系界面活性剤とし
て市販の水成膜泡消火薬剤を使用した結果、室温で懸濁
物が生じ65 CK加温後放冷すると層分離をおこした
。このように市販の水成Il&池消大基剤を水成膜形成
機械泡消火薬剤に使用して実用性の高いものとするには
かかる問題点の解決が必要である。
Water-Based Fire Extinguishing Agent Regarding the above example, an attempt is made to apply it to a water film forming mechanical foam fire extinguishing agent.If a commercially available water film forming foam fire extinguishing agent is mixed as a fluorosurfactant, I! If left in a cloudy state, layer separation occurred and it became unusable. or,
In the case of examples (1) and (2) above, where a fire extinguishing agent using a fluorine-based surfactant is proposed, suspensions are formed at room temperature as a result of using a commercially available water-forming foam extinguishing agent as a fluorine-based surfactant. When 65CK was heated and allowed to cool, layer separation occurred. As described above, it is necessary to solve these problems in order to make the commercially available aqueous Il and pond extinguishing bases highly practical for use in aqueous film-forming mechanical foam fire extinguishing agents.

本発明者らは、これらの問題点について種々検討な重ね
た結果、スルファミン酸塩を用いることにより問題点を
解決できることな見出し、本発明に至った。以上で明ら
かなごとく、本発明の目的は、ム火災に対して^い消火
能力を保持し、低温および高温においても、安定な水成
J[形成高性能機械泡消火薬剤を提供することである。
As a result of various studies on these problems, the present inventors discovered that the problems could be solved by using sulfamate, and arrived at the present invention. As is clear from the above, an object of the present invention is to provide a high-performance mechanical fire extinguishing foam that maintains high fire extinguishing ability against fires and is stable even at low and high temperatures. .

本発明の泡消火薬剤は、スルファミン酸アンモニウムと
尿素を主成分とし、フッ素系界面活性剤を含有する水溶
液であることを特徴とする。
The fire extinguishing foam of the present invention is characterized in that it is an aqueous solution containing ammonium sulfamate and urea as main components and a fluorosurfactant.

本発明における消火薬剤100−のスルファイン酸アン
モニウムの含有ili#i、5〜40fであり、スルフ
ァミン酸アンモニク、ムと尿素の合計含有量は、15f
以上でるる。また、スルファイン酸アンモニウムに対す
る尿素の重量比は。
The content of ammonium sulfate in the fire extinguishing agent 100 in the present invention is 5 to 40 f, and the total content of ammonium sulfamate, mu and urea is 15 f.
That's all. Also, what is the weight ratio of urea to ammonium sulfate?

0.5〜10である。It is 0.5-10.

本発明の泡消火薬剤は、水溶性rミンを酪加して処理で
れることにより、更に安定性の高いものとなる。その方
法はスルファミン酸アンモ二tム水溶液に水溶性アきン
を加えて攪拌又は加熱梳拌する(とにより、発生するア
ンモニアガスを追出して後、尿素、フッ素糸界面活性剤
、水などを混合する方法。スルファミン酸アンモエクム
、尿素、7ツ票系昇WI活性剤、などから1にる水S*
に水溶性アミンを添加し親会することによ夕夷生するア
ンモニアガスを除去する方法。水溶性アンンとスルファ
ンン酸な反応させて後、スルファずン酸アンモニウム1
m、7ツS*昇面活性剤、を混合す為方法、スルファ電
ン駿アンン、スルファ電ン酸アンモニクム。
The foam fire extinguishing agent of the present invention becomes even more stable by adding water-soluble rmin to the treatment. The method is to add a water-soluble aqueous solution to an aqueous solution of ammonium sulfamate and stir or heat and comb (to expel the generated ammonia gas, then mix urea, fluorine thread surfactant, water, etc.) Method: Water S* made from ammoecium sulfamate, urea, 7-base WI activator, etc.
A method of removing ammonia gas produced by adding a water-soluble amine to the mixture. After reacting water-soluble ammonium with sulfanoic acid, ammonium sulfazunate 1
Method for mixing m, 7 S* surface active agents, sulfaelectron, ammonicum sulfaelectroate.

尿素、フッ素系界面活性剤を混合する方法碌どかある。There are many ways to mix urea and fluorosurfactants.

本発明における水溶性アインの処理によって、スルファ
建ン酸アンモニウムの1部又は大部分な水溶性アミンの
塩KRき換わシ、更に安定性の高いll11iI火薬剤
となる。
By the treatment of water-soluble eine in the present invention, part or most of the water-soluble ammonium sulfanophosphate is converted to the water-soluble amine salt KR, resulting in a more stable ll11iI explosive.

水S性ア電ンとして使用されるものとしては、メチルア
しヘエチルア建ン、グチ^アをンなどのアルキルアイン
(ただし毫)、ジオトリの各1ルキ身アZンも含む)、
エタノールアンン。
Those used as aqueous alkyl amines include alkylaines such as methyl amines, glutinous amines, etc.;
Ethanol ann.

グ■パノーhア建ン、ゲタノールア電ンなどリアルカッ
−ルアギン(ただし、モノ、ジ、)νの各アルカノール
アミンを含む)、メトキシグミビルアミン、エトキシプ
ロピルアミンなどの7x’3キシアミンなどの各種アミ
ンである。
Various amines such as realkalkanolamines (including mono-, di-, and)-v alkanolamines such as panolamine, getanolamine, etc., 7x'3xyamines such as methoxygumiviramine, and ethoxypropylamine. It is.

本Ji@において使J1されふ水S性1ζノの量は、低
温及び高温における安定性?I−保つための最少量で十
分であル、1%以下でも効果を発揮で蟲る。又、水溶性
アミンの使用量を多くすることにより低温及び高温にお
ける安定性な−JIljll&<できるが水溶性有機ア
ミンは可tAaであるので消火効果を妨げない程度の量
としなければならない七の量は消火薬剤全体の3096
以下ll1ILに保つことが必畳である。通常の使用量
としては1チから15%程度が好着しい。
Is the amount of water S property 1ζ used in this book J1 stable at low and high temperatures? The minimum amount needed to maintain I- is sufficient, but even less than 1% is effective. In addition, by increasing the amount of water-soluble amine used, stability at low and high temperatures can be improved, but since water-soluble organic amines are tAa, the amount must be kept at a level that does not impede the fire extinguishing effect. is 3096 of all fire extinguishing agents
It is essential to keep it at 11IL below. The amount usually used is preferably about 1 to 15%.

本抛明の辱消火薬剤の調製は、所定のものを混合、攪拌
すれφよく、いかなる方法でもよい。
The fire extinguishing agent of this invention may be prepared by any method as long as the prescribed ingredients are mixed and stirred.

攪拌は、iui、加熱(10口℃以下)いずれでもよい
。また、必′IsK応じて他の添加剤【加えてlil製
してもよい。
Stirring may be performed by IUI or by heating (at 10 °C or less). In addition, other additives may be added as required.

そり添加剤としては、酢酸カリウ^、鯵駿アンモエクム
、プはピオン駿ナトツウ五などの低級脂訪鐵のア身力V
塩、エチレングリ;−ル。
As a warping additive, potassium acetate, horse mackerel ammoekum, puwa pion shun natotsuugo, etc.
Salt, ethylene glycol.

10ビレンダツコール、グリ竜リン、トリエチレングリ
コ−J−などの多価1声コール、アルギン酸ナトリウム
、ポリアクリル酸及びそのナトリウム塩などの水溶性高
分子、塩化!グネシクム、塩化ナトリウム、塩化アンモ
ニウムなどの水溶性無機塩を単独又は複数組み合せたも
のなどをあけることができる。これらの添加剤を加える
ことにより、なお、一層広い温度範1iにおいて安定性
を増したものを得ることがで龜る。
10 Birendatucol, Glyryurin, triethylene glycol-J- and other polyvalent monophonic coals, sodium alginate, polyacrylic acid and its sodium salt, and other water-soluble polymers, chloride! Water-soluble inorganic salts such as gnesicum, sodium chloride, and ammonium chloride may be used alone or in combination. By adding these additives, it is still possible to obtain products with increased stability over a wider temperature range 1i.

本発明9フッ素系界面活性剤を含有する機械泡消火薬剤
は、A火災、B火實共に41めて禍い請人能力を保持し
、かつ低温および高温時の安定性が極めて大で例えば−
20℃以下、+70℃以上でも安定なものも得ることが
できる。又、本発明の泡消火薬剤をM濁物の生ずる湿灰
以上にm温してl5tI#倫を発生基せても放冷し温度
を下げm濁物が止じたii*以下とすると層分離するこ
となく再び透明な水溶液にもどろので夾用土支#t−き
たすことはない。
The mechanical foam extinguishing agent containing the 9 fluorine-based surfactant of the present invention maintains the ability to fight both fires A and B, and has extremely high stability at low and high temperatures, such as -
Stable products can also be obtained at temperatures below 20°C and above +70°C. In addition, even if the foam fire extinguishing agent of the present invention is heated to a temperature higher than the wet ash at which M turbidity is generated and 15tI#Lin is generated, if it is allowed to cool and the temperature is lowered to below ii* where mturbidity has stopped, the layer It will not cause any damage as it will turn back into a clear aqueous solution without separating.

以下に本発明荀実施告、比較例で説明する。The present invention will be described below with reference to practical implementation and comparative examples.

高温での安定性の評1優方法として履濁物が生ずる亀*
Va*として表現し以下に記す測定方法によって測定し
、高温でのIfk*!!を評価した。
Tortoise that produces turbidity as an excellent method for stability at high temperatures *
Expressed as Va* and measured by the measurement method described below, Ifk*! at high temperature! ! was evaluated.

凝禰点 「消火17h、m大電画の検定11JIIJに基づいて
測定した。
Condensation point "Extinguishing 17 hours, m Daidenga's certification 11JIIJ was measured.

′消火試験 「消大器の技術上の規格を定める省令J Kmづ龜ム火
災及びB大笑の試験を行った。
``Fire extinguishing test ``Ministerial ordinance that stipulates technical standards for fire extinguishers J Km zumu fire and B large fire tests were conducted.

画点 試料鞠100−をビーカーに採敗し、ゆっ(9と麹を立
てないように攪拌しながら、外部より加熱、昇温する。
Pour the image sample ball 100- into a beaker, and slowly heat and raise the temperature from the outside while stirring to prevent the koji from standing up.

加熱昇温によシ液が濁ったら加熱を中止しつぎに!2!
冷しなからsgpcの消え為温度を測定しこの温度を曇
点とする。
If the liquid becomes cloudy due to heating, stop heating and try again! 2!
After cooling, the sgpc disappears, so the temperature is measured and this temperature is taken as the cloud point.

実膣fi1〜4 スルファミン酸アンモエクム、尿素、グルピレングリフ
−身、およびフッ嵩M界面活性剤の所定量(j1!i)
に水を加えて攪拌混合し1oLの水溶液とし、水成腹影
成機械抱消火薬剤なり〈つた。
Real vagina fi1-4 Predetermined amounts of ammoecium sulfamate, urea, glupylene glyph, and fluoro-bulk M surfactant (j1!i)
Water was added to the mixture and mixed with stirring to make a 10L aqueous solution, which was then used as a water extinguishing agent.

#泡消火薬剤の物性の測定結果を表1に示す。# Table 1 shows the measurement results of the physical properties of the foam fire extinguishing agent.

実施例1,3.4で得られた泡消火薬剤を65CK加熱
後、放冷すると、画点以下で透明となった。
When the fire extinguishing foam obtained in Examples 1 and 3.4 was heated for 65 CK and then allowed to cool, it became transparent below the image point.

表  1 本2)                      
  I 5%本5)                
      l”C−200比較例1,2 実施例3のスルファミン酸アンモニウムの代わDKil
駿アンモニウム(比較例1)、または、リン酸1アンモ
ニウムとリンl112アンモニウムの1=1混合物(比
較例2)を使用し、他は同様にして表2の配合で行った
が、攪拌、混合によシ懸濁、不溶物が止じて、静置後、
層分離ををおこした。それ放物性値/Ii測定できなか
った。
Table 1 Book 2)
I 5% Book 5)
l”C-200 Comparative Examples 1 and 2 DKil instead of ammonium sulfamate in Example 3
Shun ammonium (Comparative Example 1) or a 1=1 mixture of 1 ammonium phosphate and 112 ammonium phosphorus (Comparative Example 2) was used, and the other formulations were the same as shown in Table 2. After the suspension and insoluble matter have stopped and it is allowed to stand still,
Layer separation occurred. It was not possible to measure the parabolic value/Ii.

比較例3 実施例3において、〆Xを便用せず、スルフ7<ン酸ア
ンモニウムv、/sbとし、他は同様に行った。結果を
表2に示す。
Comparative Example 3 The same procedure as in Example 3 was carried out except that 〆X was omitted and ammonium sulfur 7< phosphate v,/sb was used. The results are shown in Table 2.

表  2 本6) 常温微温 実施例5〜12 表3の配合で混合、攪拌して10Lの水溶液とし、水成
膜形成機械泡消火薬剤をつくった。
Table 2 Book 6) Room Temperature and Low Temperature Examples 5 to 12 The formulations shown in Table 3 were mixed and stirred to form a 10 L aqueous solution to produce a water film forming mechanical foam fire extinguishing agent.

その物性の掬定結果を表3に示す。Table 3 shows the results of determining the physical properties.

比較f14〜7 表4の配合で混合、攪拌したが、常温で懸濁し、低温で
は透明にならなかった。65℃加熱後、層分離を起した
。それ故、物性は測定できなかった。
Comparison f14-7 Although the mixture was mixed and stirred according to the formulation shown in Table 4, it was suspended at room temperature and did not become transparent at low temperature. After heating to 65°C, layer separation occurred. Therefore, physical properties could not be measured.

Claims (1)

【特許請求の範囲】 41)ス身ファiン酸アンモニクムと尿素を主g分とし
、フッ素系界面活性剤を含有する水溶液であることを特
徴とすみ水成m形成機械泡消火薬剤。 (2)水@1lvc水濤性アミンを添加して!A11さ
れた特許請求の範i1m $1 (1)項記載の泡消火
薬剤。 (3)水筒性アミンでI&型されたスルファミン駿アン
モニクムを特徴とする特許請求の範囲嬉(1)項記載の
泡消火薬剤。 (4)水S法ア建ンとスにファンン駿を反応させて添加
された特許請求のll1ll蕗(1)項記載の泡消火薬
剤。 優)水11性アンンを消火薬剤全体の30重量−以下に
なゐよ5に添加ぢれた特許請求の範sM(2)項ないし
第(4)項記載の池消火鶴剤。 (6)低級脂肪酸のアルカリ塩、多価アルコール、水#
!!に高分子化合物、および水溶性無機塩から選ばれた
1櫨または2種以上のものを含む特許請求の範囲III
 (1)項ないし菖俤)項記載の1消火薬剤。
[Scope of Claims] 41) A mechanical foam fire extinguishing agent which is characterized in that it is an aqueous solution containing ammonium fernate and urea as main components and a fluorine surfactant. (2) Add water @ 1 lvc water-borne amine! A11 Claim i1m $1 The foam fire extinguishing agent described in item (1). (3) The fire extinguishing foam agent according to claim (1), which is characterized by sulfamine ammonicum which is I& type with a canteen amine. (4) The foam fire extinguishing agent according to claim (1), which is added by reacting fannshun to water S method Aken and Su. Excellent) A pond fire extinguishing agent according to claims sM(2) to (4), wherein water is added to an amount of less than 30% by weight of the entire extinguishing agent. (6) Alkaline salts of lower fatty acids, polyhydric alcohols, water #
! ! Claim III containing one or more selected from a polymer compound and a water-soluble inorganic salt.
1. Extinguishing agent described in (1) to (1) to (1).
JP12907181A 1981-08-18 1981-08-18 fire extinguishing foam Expired JPS6019254B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12907181A JPS6019254B2 (en) 1981-08-18 1981-08-18 fire extinguishing foam

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12907181A JPS6019254B2 (en) 1981-08-18 1981-08-18 fire extinguishing foam

Publications (2)

Publication Number Publication Date
JPS5829473A true JPS5829473A (en) 1983-02-21
JPS6019254B2 JPS6019254B2 (en) 1985-05-15

Family

ID=15000357

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12907181A Expired JPS6019254B2 (en) 1981-08-18 1981-08-18 fire extinguishing foam

Country Status (1)

Country Link
JP (1) JPS6019254B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008132655A (en) * 2006-11-28 2008-06-12 Sankyo:Kk Method and device for binding paper sheet
DE102013111142A1 (en) * 2013-10-09 2015-04-09 Jens Volker Habermann Method for increasing the efficiency of a fire-extinguishing liquid

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008132655A (en) * 2006-11-28 2008-06-12 Sankyo:Kk Method and device for binding paper sheet
DE102013111142A1 (en) * 2013-10-09 2015-04-09 Jens Volker Habermann Method for increasing the efficiency of a fire-extinguishing liquid

Also Published As

Publication number Publication date
JPS6019254B2 (en) 1985-05-15

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