JPS6370B2 - - Google Patents
Info
- Publication number
- JPS6370B2 JPS6370B2 JP57229177A JP22917782A JPS6370B2 JP S6370 B2 JPS6370 B2 JP S6370B2 JP 57229177 A JP57229177 A JP 57229177A JP 22917782 A JP22917782 A JP 22917782A JP S6370 B2 JPS6370 B2 JP S6370B2
- Authority
- JP
- Japan
- Prior art keywords
- fire
- tempura oil
- fire extinguishing
- extinguishing
- 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
- 239000003795 chemical substances by application Substances 0.000 claims description 31
- 239000000203 mixture Substances 0.000 claims description 20
- 239000003513 alkali Substances 0.000 claims description 16
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 14
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 239000002562 thickening agent Substances 0.000 claims description 4
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 2
- 229920000615 alginic acid Polymers 0.000 claims description 2
- 235000010443 alginic acid Nutrition 0.000 claims description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims description 2
- 150000004676 glycans Chemical class 0.000 claims description 2
- 229920001282 polysaccharide Polymers 0.000 claims description 2
- 239000005017 polysaccharide Substances 0.000 claims description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 2
- 239000003921 oil Substances 0.000 description 32
- 235000019198 oils Nutrition 0.000 description 32
- 239000006260 foam Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
- 239000007788 liquid Substances 0.000 description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical group [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
- 239000002075 main ingredient Substances 0.000 description 5
- 238000007127 saponification reaction Methods 0.000 description 5
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- -1 monobromide monochloride difluoride methane Chemical compound 0.000 description 3
- 229910000027 potassium carbonate Inorganic materials 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 2
- 244000144972 livestock Species 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- GEHMBYLTCISYNY-UHFFFAOYSA-N Ammonium sulfamate Chemical compound [NH4+].NS([O-])(=O)=O GEHMBYLTCISYNY-UHFFFAOYSA-N 0.000 description 1
- MRCUIHOYPYOMEL-UHFFFAOYSA-N C.F.F.F.Br Chemical compound C.F.F.F.Br MRCUIHOYPYOMEL-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- FZQSLXQPHPOTHG-UHFFFAOYSA-N [K+].[K+].O1B([O-])OB2OB([O-])OB1O2 Chemical compound [K+].[K+].O1B([O-])OB2OB([O-])OB1O2 FZQSLXQPHPOTHG-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000007798 antifreeze agent Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical group 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- WUUHFRRPHJEEKV-UHFFFAOYSA-N tripotassium borate Chemical compound [K+].[K+].[K+].[O-]B([O-])[O-] WUUHFRRPHJEEKV-UHFFFAOYSA-N 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Landscapes
- Fire-Extinguishing Compositions (AREA)
Description
本発明は、圧力容器より噴霧状で放射する安全
で速消性を有する消火剤組成物に関する。
近年、家庭でのてんぷら油火災が激増してい
る。このてんぷら油は、グリセリンと多種の飽和
又は不飽和脂肪酸とで構成されるエステルを一般
組成とするもので、通常の使用温度である170〜
190℃では種火を近づけても引火する惧れは全く
ない。しかしながら、約260℃の引火点以上に加
熱すると、表面からてんぷら油の蒸気や分解ガス
が出てくるため、種火を近づけると容易に引火す
るようになり、更に約360℃の発火点を超えると、
てんぷら油の蒸気や分解ガスが多量に発生し、種
火がなくても着火して火災を起すようになる。
ところで、従来の消火剤には、大別してガス系
のもの、蒸発性液体系のもの、粉末系のもの、水
系のもの、泡系のものがあり、これらは夫々の特
性により火災対象物に応じて適宜使い分けされて
いるが、いずれの消火剤も、てんぷら油が発火点
以上で燃焼している場合には、以下に述べるよう
に満足な消火を行なうことが困難である。
即ち、炭酸ガス消火剤などのガス系の消火剤
や、一臭化三フツ化メタン、一臭化一塩化二フツ
化メタン、二臭化四フツ化エタンなどの蒸発性液
体系の消火剤は、その放射中はてんぷら油火災を
消火できるが、てんぷら油の温度を発火点以下に
下げる冷却作用がなく、且つてんぷら油からの可
燃性蒸気の放出を抑制する作用もないため、消火
剤の放射を止めると直ちに再着火し、消火不能で
ある。
また、重炭酸アルカリ塩や、重炭酸アルカリ塩
と尿素との反応生成物などを主剤とする粉末系の
消火剤は、てんぷら油をわずかにケン化しててん
ぷら油の表面に薄い皮膜を形成するが、この皮膜
によつててんぷら油からの可燃性蒸気の放出を抑
制するまでには至らず、しかも上記のガス系消火
剤や蒸発性液体系消火剤と同様に冷却作用がない
ため、再着火を防止するには相当量の粉末が必要
であり、通常家庭で使用される消火器に充填され
る量では不充分である。
更に、たん白泡消火剤、合成界面泡消火剤、水
成膜泡消火剤などによつて代表される泡系の消火
剤は、てんぷら油の冷却作用や可燃性蒸気の抑制
作用にはすぐれているが、泡放射時に火をあおつ
たり(フラツシユオーバー現象)、てんぷら油を
飛散させたりするので非常に危険である。
上記4種の消火剤に較べ、水系の消火剤の代表
例の一つである炭酸カリウムを主剤とする強化液
消火剤は、主剤の炭酸カリウムが重炭酸アルカリ
塩よりは強アルカリ性でケン化作用が若干強く可
燃性蒸気の放出をある程度抑制することが可能で
あり、且つてんぷら油の冷却作用も有するところ
から、てんぷら油火災には比較的有効と考えられ
ているが、この強化液消火剤とても、再着火を完
全に防止するには可燃性蒸気の抑制作用がまだま
だ不充分であり、しかも炭酸カリウムを30重量%
以上も含有した濃厚溶液でPH12.4以上とアルカリ
性が強く人畜に危険を及ぼすところから、消火剤
として充分満足し得るものとは到底言い難い。
本発明は斯る事情に鑑みてなされたもので、消
防法に定めるA火災(普通火災)、B火災(油火
災)及びC火災(電気火災)を有効に消火するこ
とはもとより、近年多発しているてんぷら油火災
を安全且つ迅速に消火してその再着火を充分に防
止できる弱アルカリ性の消火剤組成物を提供しよ
うとするものである。
即ち、本発明の消火剤組成物は、重炭酸アルカ
リ塩6〜15重量%とホウ酸塩2〜10重量%が主剤
として水に溶解せしめられたもので、火災発生時
に圧力容器から噴霧状で放射することにより、消
火を行なうものである。
重炭酸アルカリ塩を単独で水等の溶媒に溶解し
た溶液は弱アルカリ性であり、既述したようにて
んぷら油をわずかにケン化しててんぷら油の表面
に薄い皮膜を形成するが、てんぷら油からの可燃
性蒸気の放出を完全に抑制できる丈夫で耐久性の
ある泡をてんぷら油の表面に形成する働きはな
く、且つてんぷら油の温度を発火点以下に下げる
働きもない。また、ホウ酸塩の単独溶液の場合
も、上記の働きはない。
然るに、本発明のように重炭酸アルカリ塩6〜
15重量%とホウ酸塩2〜10重量%を混合して水に
溶かした消火剤組成物であれば、噴霧状で少量放
射するだけで、発火点以上の高温で燃焼している
てんぷら油の表面に丈夫で耐久性のある泡を急速
に形成し、てんぷら油火災を瞬時に消火すると共
にてんぷら油からの可燃性蒸気の放出を抑制し、
放射後の再着火を充分に防止することができるの
である。このことは本発明者が種々研究を重ねた
結果、初めて見出した知見であつて、おそらく
は、重炭酸アルカリ塩によるてんぷら油のケン化
作用が共存するホウ酸塩によつて著しく促進され
るために、可燃性蒸気の放出を完全に抑制するに
足る丈夫で耐久性のある泡が急速に形成されるも
のと推察される。
本発明に用いる重炭酸アルカリ塩としては、例
えば重炭酸カリウム、重炭酸ナトリウム等の水溶
性重炭酸アルカリ塩が好適であり、また、ホウ酸
塩としては、一般式M2O・mB2O3〔但し、式中M
はアルカリ金属をあらわし、mは1から4の間の
値をとる〕で示される。例えばホウ酸カリウム、
ホウ酸ナトリウム、四ホウ酸カリウム等の水溶性
ホウ酸塩が好適である。そして、これらの含有率
は、後述の実施例で示すように、重炭酸アルカリ
塩が約6〜15重量%、ホウ酸塩が約2〜10重量%
の範囲となるようにする。これは、重炭酸アルカ
リ塩が6重量%に満たず、ホウ酸塩が2重量%に
満たない場合は、重炭酸アルカリ塩が不足すると
共にホウ酸塩によるケン化促進作用も顕著に行な
われないため、てんぷら油の表面に充分な量の泡
を形成させることが困難となり、逆に重炭酸アル
カリ塩が15重量%を超え、ホウ酸塩が10重量%を
超える場合は、過剰量の泡が形成される無駄があ
ると共に消火剤自体のアルカリ性も幾分かは強く
なるという不都合が生じるからである。
本発明の消火剤組成物は、上記のように重炭酸
アルカリ塩とケン化促進作用を行なうホウ酸塩と
を主剤とするものであるが、望ましくは、これら
主剤間の化学反応を惹起しない、カルボキシメチ
ルセルロース、ポリビニルアルコール、多糖類、
アルギン酸塩よりなる群から選ばれる一種又は二
種以上の増粘剤を更に添加してやるのがよい。斯
る増粘剤を添加すると、てんぷら油の表面に形成
される泡の層がより丈夫で耐久性のよいものとな
るからである。なお、斯る増粘剤は1重量%未満
の極く少量を添加するだけで充分である。
更に本発明消火剤組成物は、凝固点を下げる目
的で尿素等の不凍剤を添加したり、或は消防法に
定めるA火災の消火能力を高める目的で硫酸アン
モニウムやスルフアミン酸アンモニウム及びリン
酸アンモニウムを添加したり、或は消防法に定め
るB火災の消火能力を高める目的でクエン酸、酢
酸、酒石酸等の有機酸のアルカリ塩やハロゲン化
アルカリ塩を添加したりすることも勿論可能であ
る。これらの添加剤はいずれもケン化作用や消火
力を低下させる惧れのないものであるから、夫々
の目的に応じて自由に添加量を決定することがで
きる。
次に実施例を挙げて本発明消火剤組成物を説明
する。
実施例 1〜6
下記第1表に示す組成割合の6種の消火剤組成
物を調製し、各組成物をエアゾール式簡易消火具
に300gづつ充填して液化ガスで加圧し、次の要
領でてんぷら油火災の消火試験を行なつた。
直径30cm、深さ7.5cmの中華鍋に700mlの大豆油
(発火点が360〜370℃の範囲のもの)を入れ、ガ
スコンロで400℃まで加熱して大豆油を燃焼させ、
ガスコンロの火を消してから消火具又はエアゾー
ル式簡易消火具より消火剤組成物を噴霧状で放射
を開始し、消火終了後さらに5秒間連続放射した
後、再着火の有無とてんぷら油の表面の状態を観
察した。
この消火試験の結果を下記第2表に示す。
更に、各消火剤組成物を3型消火器に充填
し、消防法に定めるA―1単位及びB―2単位の
消火試験をしたところ、いずれの組成物も合格で
あつた。
比較例 1〜3
下記第1表に示す組成割合の3種の消火剤組成
物について、上記実施例と同じ要領でてんぷら油
火災の消火試験を行なつた。その結果を下記第2
表に併せて示す。
The present invention relates to a safe and quickly extinguishing fire extinguishing agent composition that is emitted in spray form from a pressure vessel. In recent years, the number of tempura oil fires in homes has increased dramatically. This tempura oil has a general composition of esters consisting of glycerin and various saturated or unsaturated fatty acids, and has a normal usage temperature of 170 -
At 190℃, there is no risk of ignition even if a pilot flame is brought close. However, when heated above the flash point of approximately 260 degrees Celsius, steam and decomposition gas from the tempura oil will come out from the surface, which will easily ignite when brought close to the pilot flame, and will further exceed the ignition point of approximately 360 degrees Celsius. and,
A large amount of steam and decomposed gas from the tempura oil is generated, which can ignite and cause a fire even without a pilot flame. By the way, conventional extinguishing agents can be roughly divided into gas-based, evaporative liquid-based, powder-based, water-based, and foam-based, and these have their own characteristics depending on the object of fire. However, when tempura oil burns above its ignition point, it is difficult for any of these extinguishing agents to satisfactorily extinguish the fire, as described below. In other words, gas-based extinguishing agents such as carbon dioxide extinguishing agents, and evaporative liquid-based extinguishing agents such as monobromide trifluoride methane, monobromide monochloride difluoride methane, dibromide tetrafluoride ethane, etc. , it is possible to extinguish a tempura oil fire while it is being radiated, but it does not have the cooling effect of lowering the temperature of tempura oil below its ignition point, nor does it have the effect of suppressing the release of flammable vapor from tempura oil. If the fire is stopped, the fire will re-ignite immediately and cannot be extinguished. In addition, powder-based fire extinguishers whose main ingredients are alkali bicarbonate or the reaction product of alkali bicarbonate and urea slightly saponify the tempura oil and form a thin film on the surface of the tempura oil. However, this film does not go so far as to suppress the release of flammable vapor from the tempura oil, and like the gas-based extinguishing agents and evaporative liquid-based extinguishing agents mentioned above, it does not have a cooling effect, so it does not prevent re-ignition. A considerable amount of powder is required to prevent this, and the amount normally filled in a fire extinguisher used at home is insufficient. Furthermore, foam-based fire extinguishing agents, such as protein foam fire extinguishing agents, synthetic interfacial foam fire extinguishing agents, and aqueous film-forming foam fire extinguishing agents, have excellent cooling effects on tempura oil and suppressing flammable vapors. However, it is extremely dangerous as it can fan the flames (flashover phenomenon) and scatter tempura oil when emitting foam. Compared to the above four types of extinguishing agents, a reinforced liquid extinguishing agent whose main agent is potassium carbonate, which is one of the representative examples of water-based extinguishing agents, has a saponification effect because the main agent potassium carbonate is more alkaline than alkali bicarbonate. This enhanced liquid fire extinguisher is considered to be relatively effective against tempura oil fires because it is somewhat strong and can suppress the release of flammable vapor to some extent, and also has the cooling effect of tempura oil. However, the suppressing effect on flammable vapors is still insufficient to completely prevent re-ignition, and the potassium carbonate content is 30% by weight.
It is a concentrated solution containing the above, with a pH of 12.4 or higher, which is highly alkaline and poses a danger to humans and livestock, so it is far from satisfactory as a fire extinguisher. The present invention has been made in view of the above circumstances, and is effective in extinguishing fires A (ordinary fire), fire B (oil fire), and fire C (electrical fire) stipulated in the Fire Service Act, as well as fires that have been occurring frequently in recent years. The present invention aims to provide a weakly alkaline fire extinguishing agent composition that can safely and quickly extinguish tempura oil fires and sufficiently prevent re-ignition. That is, the fire extinguishing composition of the present invention has 6 to 15% by weight of an alkali bicarbonate and 2 to 10% by weight of a borate dissolved in water as main ingredients, and is sprayed from a pressure vessel in the event of a fire. It extinguishes fire by emitting radiation. A solution prepared by dissolving alkaline bicarbonate alone in a solvent such as water is weakly alkaline, and as mentioned above, it slightly saponifies tempura oil and forms a thin film on the surface of tempura oil. It does not work to form strong and durable bubbles on the surface of the tempura oil that can completely suppress the release of flammable vapors, nor does it work to lower the temperature of the tempura oil below its ignition point. Furthermore, a solution of borate alone does not have the above effect. However, as in the present invention, alkali bicarbonate 6~
A fire extinguishing agent composition made by mixing 15% by weight and 2 to 10% by weight of borate and dissolving it in water can be used to destroy tempura oil burning at a high temperature above the ignition point by just emitting a small amount in spray form. Rapidly forms strong and durable foam on the surface, instantly extinguishing tempura oil fires and suppressing the release of flammable vapors from tempura oil.
Re-ignition after radiation can be sufficiently prevented. This was the first discovery made by the inventor after various studies, and is probably because the saponification of tempura oil by alkali bicarbonate is significantly accelerated by the coexisting borate. It is assumed that a foam strong and durable enough to completely suppress the release of flammable vapors would form rapidly. As the alkali bicarbonate salt used in the present invention, water-soluble alkali bicarbonate salts such as potassium bicarbonate and sodium bicarbonate are suitable . [However, M in the formula
represents an alkali metal, and m takes a value between 1 and 4. For example, potassium borate,
Water-soluble borates such as sodium borate and potassium tetraborate are preferred. As shown in the examples below, the content of these is approximately 6 to 15% by weight for alkali bicarbonate and approximately 2 to 10% by weight for borate.
be within the range of This is because if the amount of alkali bicarbonate is less than 6% by weight and the amount of borate is less than 2% by weight, there will be a shortage of alkali bicarbonate and the borate will not have a significant saponification promoting effect. Therefore, it becomes difficult to form a sufficient amount of bubbles on the surface of tempura oil. Conversely, if the alkali bicarbonate content exceeds 15% by weight and the borate content exceeds 10% by weight, an excessive amount of bubbles may form. This is because there is a disadvantage that there is waste formed and the alkalinity of the extinguishing agent itself becomes somewhat stronger. The fire extinguishing agent composition of the present invention contains an alkali bicarbonate and a borate that promotes saponification as main ingredients as described above, but desirably does not cause a chemical reaction between these main ingredients. Carboxymethyl cellulose, polyvinyl alcohol, polysaccharides,
It is preferable to further add one or more thickeners selected from the group consisting of alginates. This is because when such a thickener is added, the foam layer formed on the surface of tempura oil becomes stronger and more durable. Incidentally, it is sufficient to add such a thickening agent in a very small amount of less than 1% by weight. Furthermore, the fire extinguishing composition of the present invention may contain an antifreeze agent such as urea for the purpose of lowering the freezing point, or may contain ammonium sulfate, ammonium sulfamate, and ammonium phosphate for the purpose of increasing the ability to extinguish A fires stipulated in the Fire Service Act. Of course, it is also possible to add an alkali salt of an organic acid such as citric acid, acetic acid, or tartaric acid or an alkali halide salt for the purpose of increasing the ability to extinguish B fires specified in the Fire Service Act. Since all of these additives are free from the risk of reducing the saponification effect or fire extinguishing power, the amount to be added can be freely determined depending on the purpose. Next, the fire extinguishing agent composition of the present invention will be explained with reference to Examples. Examples 1 to 6 Six types of fire extinguishing agent compositions having the composition ratios shown in Table 1 below were prepared, and 300 g of each composition was filled into an aerosol type simple fire extinguisher, pressurized with liquefied gas, and heated in the following manner. We conducted a fire extinguishing test for a tempura oil fire. Pour 700ml of soybean oil (with an ignition point in the range of 360 to 370℃) into a wok with a diameter of 30cm and a depth of 7.5cm, heat it to 400℃ on a gas stove, and burn the soybean oil.
After extinguishing the fire on the gas stove, start spraying a fire extinguishing agent composition from a fire extinguisher or a simple aerosol fire extinguisher, and after extinguishing the fire, continue spraying for another 5 seconds, and then check whether there is any re-ignition and the surface of the tempura oil. I observed the condition. The results of this fire extinguishing test are shown in Table 2 below. Furthermore, when each of the fire extinguishing agent compositions was filled into a Type 3 fire extinguisher and subjected to the A-1 unit and B-2 unit fire extinguishing tests stipulated in the Fire Service Act, all compositions passed. Comparative Examples 1 to 3 A test for extinguishing a tempura oil fire was carried out in the same manner as in the above example for three types of fire extinguishing agent compositions having the composition ratios shown in Table 1 below. The results are shown in the second section below.
It is also shown in the table.
【表】【table】
【表】【table】
【表】
上記第1表を見れば、本発明の消火剤組成物は
重炭酸アルカリ塩とホウ酸塩を主剤とする低濃度
溶液であり、従来の酸カリウム濃厚溶液の強化液
消火剤(比較例3)に較べると遥かにアルカリ性
が弱く、人畜に危険を及ぼす惧れの少ないもので
あることが判る。そして第2表を見れば、約200
g以下の少ない使用量であるにも拘らず、数秒の
うちに消火しててんぷら油の表面に厚い泡の層を
形成し、てんぷら油からの可燃性蒸気の放出を抑
制して再着火を完全に防止する、消火能力及び再
着火防止能力に優れた消火剤組成物であることが
判る。[Table] Looking at Table 1 above, it can be seen that the fire extinguishing agent composition of the present invention is a low concentration solution containing alkali bicarbonate and borate as main ingredients, and the conventional reinforced liquid extinguishing agent of concentrated acid potassium solution (compared to It can be seen that it is far less alkaline than Example 3) and is less likely to pose a danger to humans and livestock. And if you look at Table 2, about 200
Even though the amount used is small (less than 1 gram), it extinguishes the fire within seconds and forms a thick layer of foam on the surface of the tempura oil, suppressing the release of flammable vapor from the tempura oil and completely preventing re-ignition. It can be seen that the fire extinguishing agent composition has excellent fire extinguishing ability and re-ignition prevention ability.
Claims (1)
〜10重量%が主剤として水に溶解せしめられてい
ることを特徴とする消火剤組成物。 2 カルボキシメチルセルロース、ポリビニルア
ルコール、多糖類、アルギン酸塩よりなる群から
選ばれた一種又は二種以上の増粘剤を含有せしめ
た特許請求の範囲第1項記載の消火剤組成物。[Scope of Claims] 1. 6 to 15% by weight of alkali bicarbonate and borate 2.
A fire extinguishing agent composition characterized in that ~10% by weight is dissolved in water as a main agent. 2. The fire extinguishing composition according to claim 1, which contains one or more thickeners selected from the group consisting of carboxymethyl cellulose, polyvinyl alcohol, polysaccharides, and alginates.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22917782A JPS59115061A (en) | 1982-12-23 | 1982-12-23 | Fire extinguishing composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22917782A JPS59115061A (en) | 1982-12-23 | 1982-12-23 | Fire extinguishing composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59115061A JPS59115061A (en) | 1984-07-03 |
JPS6370B2 true JPS6370B2 (en) | 1988-01-05 |
Family
ID=16887996
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP22917782A Granted JPS59115061A (en) | 1982-12-23 | 1982-12-23 | Fire extinguishing composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59115061A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3901537B2 (en) * | 2001-02-16 | 2007-04-04 | ミヤケ・エンジニアリング株式会社 | Building with fire extinguishing method and fire extinguishing equipment unit |
JP4630682B2 (en) * | 2005-02-07 | 2011-02-09 | 二夫 馬場 | Fire extinguisher, fire extinguisher and flame retardant, flame proof sheet, flame retardant fiber |
JP5481033B2 (en) * | 2008-02-27 | 2014-04-23 | 能美防災株式会社 | Bubble fire extinguishing equipment |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5122298A (en) * | 1974-08-20 | 1976-02-21 | Kadota Mitsushige | Shokaekino seizoho |
-
1982
- 1982-12-23 JP JP22917782A patent/JPS59115061A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5122298A (en) * | 1974-08-20 | 1976-02-21 | Kadota Mitsushige | Shokaekino seizoho |
Also Published As
Publication number | Publication date |
---|---|
JPS59115061A (en) | 1984-07-03 |
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