JP2893038B1 - Fire extinguisher - Google Patents
Fire extinguisherInfo
- Publication number
- JP2893038B1 JP2893038B1 JP10361198A JP10361198A JP2893038B1 JP 2893038 B1 JP2893038 B1 JP 2893038B1 JP 10361198 A JP10361198 A JP 10361198A JP 10361198 A JP10361198 A JP 10361198A JP 2893038 B1 JP2893038 B1 JP 2893038B1
- Authority
- JP
- Japan
- Prior art keywords
- fire extinguishing
- halon
- coch
- fire
- extinguishing agent
- 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
Links
Abstract
【要約】
【課題】 オゾン層を破壊することがなく、また比較的
に分解しやすいことから地球温暖化に対する影響が少な
く、規制ハロンの消火能力に匹敵する代替消火薬剤を提
供する。
【解決手段】 下記一般式(1)
【化1】
(式中、nは4〜8の数を示し、mは0又は1の数を示
し、R1はメチル基又はエチル基を示す)で表される含
フッ素ケトンを主成分として用いることを特徴とする消
火薬剤。The present invention provides an alternative fire extinguishing agent that does not destroy the ozone layer and is relatively easy to decompose, has little effect on global warming, and is comparable to the fire extinguishing ability of regulated halon. SOLUTION: The following general formula (1): (Wherein, n represents a number of 4 to 8, m represents a number of 0 or 1, and R 1 represents a methyl group or an ethyl group). And extinguishing agents.
Description
【0001】[0001]
【発明の属する技術分野】本発明は含フッ素ケトンを主
成分とした消火薬剤に関するものである。さらに詳しく
は、本発明は、オゾン層を破壊する物質として使用が規
制されているハロン消火薬剤の代替品として使用される
含フッ素ケトンを主成分とした消火薬剤に関するもので
ある。TECHNICAL FIELD The present invention relates to a fire extinguishing agent containing a fluorinated ketone as a main component. More specifically, the present invention relates to a fire extinguishing agent containing a fluorine-containing ketone as a main component, which is used as a substitute for a halon fire extinguishing agent whose use is regulated as a substance that destroys the ozone layer.
【0002】[0002]
【従来の技術】従来使用されてきたフロンは、化学的に
極めて安定なため、対流圏での寿命が長く、拡散して成
層圏に達し、ここで紫外線により光分解して塩素ラジカ
ルを発生する。この塩素ラジカルが成層圏オゾンと連鎮
反応を起し、オゾン層を破壊することから、その生産が
1996年より禁止及び消費について規制が実施されて
いる。フロンの代替品としては化合物中に水素原子を導
入することにより、適当な分解性を付与したヒドロフル
オロカーボン(HFC)やヒドロクロロフルオロカーボ
ン(HCFC)が開発されている。消火薬剤としては、
従来よりハロン1301(CF3Br)、ハロン121
1(CF2BrCl)、ハロン2402(CF2BrCF
2Br)が使用されているが、消火作用に臭素が重要な
役割をはたすことから、ハロン分子中における臭素の存
在は高性能の消火作用を付与させるためには必須のもの
と考えられてきた。しかし、その中に含まれている臭素
原子がオゾン層を破壊することから、特定フロンととも
にハロンも全廃の対象となっている。近年、ハロン代替
品が開発されているが、それらは規制ハロンと比較する
と消火性能や生体に対する安全性の点においてかなり劣
るために、高度の消火能力が必要とされる航空機やコン
ピュータールームなどのような場所では規制ハロンに頼
らざるを得ない。しかし、オゾン層破壊物質であるハロ
ンはその使用が規制されている。そこでオゾン層を破壊
せず、規制ハロンと同等以上の消火性能、生体に対する
安全性などをもつ代替ハロンが必要とされている。含フ
ッ素ケトンは熱的、化学的に安定であり、生体に対する
安全性も高い。一般的には対応するペルフルオロカルボ
ン酸とグリニャール試薬との反応により合成される。含
フッ素ケトンとペルフルオロ炭化水素との化学反応性を
比較すると、前者は含有する水素原子とその構造内にも
つカルボニル結合のためにペルフルオロ炭化水素が反応
しないような条件下でも反応性を示すことが知られてい
る。すなわち、含フッ素ケトンはペルフルオロ炭化水素
と比較すると、分解性の付与された化合物であり、環境
中での寿命は短い。2. Description of the Related Art Freon, which has been conventionally used, is extremely stable chemically, has a long life in the troposphere, diffuses into the stratosphere, where it is photolyzed by ultraviolet rays to generate chlorine radicals. These chlorine radicals cause a continuous reaction with stratospheric ozone and destroy the ozone layer. Therefore, the production of the chlorine radical has been banned since 1996, and its consumption has been regulated. Hydrofluorocarbons (HFCs) and hydrochlorofluorocarbons (HCFCs) that have been given appropriate decomposability by introducing hydrogen atoms into compounds have been developed as substitutes for CFCs. As a fire extinguishing agent,
Halon 1301 (CF 3 Br) and Halon 121
1 (CF 2 BrCl), Halon 2402 (CF 2 BrCF)
2 Br) is used, but since bromine plays an important role in fire-extinguishing, the presence of bromine in halon molecules has been considered to be indispensable for imparting high-performance fire-extinguishing. . However, since the bromine atoms contained therein destroy the ozone layer, halon as well as specified CFCs have been completely eliminated. In recent years, halon substitutes have been developed, but they are considerably inferior in fire extinguishing performance and safety to living organisms as compared with regulated halon, so they are used in aircraft and computer rooms where advanced fire extinguishing capabilities are required. In places where there is no choice but to rely on the regulation Ha Long. However, the use of halon, an ozone depleting substance, is regulated. Therefore, there is a need for an alternative halon that does not destroy the ozone layer and has fire-extinguishing performance equal to or higher than that of regulated halon and safety for living bodies. Fluorinated ketones are thermally and chemically stable and highly safe for living organisms. Generally, it is synthesized by reacting the corresponding perfluorocarboxylic acid with a Grignard reagent. Comparing the chemical reactivity of fluorinated ketones with perfluorohydrocarbons, the former shows reactivity under conditions where the perfluorohydrocarbons do not react due to the contained hydrogen atom and the carbonyl bond in the structure. Are known. That is, the fluorinated ketone is a compound provided with decomposability as compared with the perfluorohydrocarbon, and has a short life in the environment.
【0003】[0003]
【発明が解決しようとする課題】本発明は、オゾン層を
破壊することがなく、また比較的に分解しやすいことか
ら地球温暖化に対する影響が少なく、規制ハロンの消火
能力に匹敵する代替消火薬剤を提供することにある。DISCLOSURE OF THE INVENTION The present invention relates to an alternative fire extinguishing agent which does not destroy the ozone layer and has relatively little effect on global warming because it is relatively easily decomposed, and which is comparable to the fire extinguishing ability of regulated halon. Is to provide.
【0004】[0004]
【課題を解決するための手段】本発明者らは代替消火薬
剤として含フッ素ケトンを使用することによりその目的
を達成し得ることを見出し、本発明を完成するに至っ
た。すなわち、本発明によれば、下記一般式(1)Means for Solving the Problems The present inventors have found that the object can be achieved by using a fluorinated ketone as an alternative fire extinguishing agent, and have completed the present invention. That is, according to the present invention, the following general formula (1)
【化1】 (式中、nは4〜8の数を示し、mは0又は1の数を示
し、R1はメチル基又はエチル基を示す)で表される含
フッ素ケトンを主成分として用いることを特徴とする消
火薬剤が提供される。Embedded image (Wherein, n represents a number of 4 to 8, m represents a number of 0 or 1, and R 1 represents a methyl group or an ethyl group). Is provided.
【0005】[0005]
【発明の実施の形態】本発明で消火薬剤として用いる含
フッ素ケトンを例示すると、CF3CF2CF2CF2CO
CH3、CF3CF2CF2CF2CF2COCH3、(C
F3)2CFCF2CF2COCH3、CF3CF2CF2CF
2CF2CF2COCH3、CF3CF2CF2CF2CF2C
F2CF2COCH3、CF3CF2CF2CF2CF2CF2
CF2CF2COCH3などの化合物が挙げられるが、好
ましくはCF3CF2CF2CF2COCH3、CF3CF2
CF2CF2CF2COCH3または、(CF3)2CFCF
2CF2COCH3が用いられる。これらのものは、その
2種以上の化合物同士を混合して使用することも可能で
ある。また、所望により、HFC−245fa等のハイ
ドロフルオロカーボンを20重量%以下の割合で混合す
ることも可能である。BEST MODE FOR CARRYING OUT THE INVENTION The fluorinated ketone used as a fire extinguishing agent in the present invention is exemplified by CF 3 CF 2 CF 2 CF 2 CO
CH 3 , CF 3 CF 2 CF 2 CF 2 CF 2 COCH 3 , (C
F 3 ) 2 CFCF 2 CF 2 COCH 3 , CF 3 CF 2 CF 2 CF
2 CF 2 CF 2 COCH 3 , CF 3 CF 2 CF 2 CF 2 CF 2 C
F 2 CF 2 COCH 3 , CF 3 CF 2 CF 2 CF 2 CF 2 CF 2
Compounds such as CF 2 CF 2 COCH 3 are mentioned, and preferably, CF 3 CF 2 CF 2 CF 2 COCH 3 , CF 3 CF 2
CF 2 CF 2 CF 2 COCH 3 or (CF 3 ) 2 CFCF
2 CF 2 COCH 3 is used. These can also be used by mixing two or more compounds. If desired, a hydrofluorocarbon such as HFC-245fa can be mixed at a ratio of 20% by weight or less.
【0006】[0006]
【実施例】次に本発明を実施例によりさらに詳細に説明
する。 実施例1 消火性能の評価は、20cm×20cm×20cmの試
験箱(アクリル製)で行った。試験箱の上部には消火剤
の導入用の小窓があり、また底部には空気導入用の小窓
が設けられた。まず、試験箱の中に置いた金属シャーレ
(直径5cm×深さ1cm)に、n−ヘプタン3mlを
入れ、7秒間予備燃焼させた。予備燃焼の間は空気導入
用の小窓を開けて、火災が十分に大きくなるようにし
た。次に予混合の消火剤を導入し、完全に消火されるま
での時間を測定することにより行った。n−C4F9CO
CH3、n−C5F11COCH3、ブロモトリフルオロメ
タン(ハロン1301)の場合の結果を表1に示す。Next, the present invention will be described in more detail with reference to examples. Example 1 Fire extinguishing performance was evaluated in a test box (made of acrylic) of 20 cm × 20 cm × 20 cm. There was a small window for the introduction of fire extinguisher at the top of the test box and a small window for the introduction of air at the bottom. First, 3 ml of n-heptane was put into a metal petri dish (diameter 5 cm × depth 1 cm) placed in a test box, and pre-burned for 7 seconds. During pre-combustion, a small window for air introduction was opened to ensure that the fire was sufficiently large. Next, a premixed extinguishing agent was introduced, and the time until the fire was completely extinguished was measured. n-C 4 F 9 CO
Table 1 shows the results in the case of CH 3 , nC 5 F 11 COCH 3 , and bromotrifluoromethane (Halon 1301).
【0007】[0007]
【表1】 ─────────────────────────── 消火剤 (vol%) 消火時間(sec) ─────────────────────────── n−C4F9COCH3 5.7 0.90 3.8 1.6 2.6 8.0 n−C5F11COCH3 3.6 0.90 2.8 7.8 CF3Br 3.6 1.0 1.1 10.0 ─────────────────────────── 表1においてフルオロケトン類は3〜5vol%の範囲
においてハロン1301と同程度で消火が可能であり、
優れた消火性能をもつことが明らかとなった。また、消
火後の試験箱内の混合気の刺激臭も少なく、ハロン13
01の場合と同程度であった。[Table 1] 火 Fire extinguisher (vol%) Fire extinguishing time (sec) ──────── N nC 4 F 9 COCH 3 5.7 0.90 3.8 1.6 1.6 2.6 8.0 nC 5 F 11 COCH 3 3.6 0.90 2.8 7.8 CF 3 Br 3.6 1.0 1.1 10.0}に お い て In Table 1, fluoroketones can extinguish fire in the same range as Halon 1301 in the range of 3-5 vol%,
It was found that it had excellent fire extinguishing performance. In addition, the irritating odor of the air-fuel mixture in the test box after the fire was extinguished was small.
01 was almost the same.
【0008】実施例2 層流燃焼速度の測定を行った。層流燃焼速度の測定に
は、内径20.0cm、高さ30.0cmの円筒型燃焼
容器を使用した。容器内に予混合気(試料混合気:9.
5%メタン−0.5%添加剤−90.0%空気;混合気
温度:室温;混合気圧力:1atm)を充填した後、中
心で火花点火し、火炎の伝播速度をイオンプローブによ
り測定した。火炎は初期段階においてほぼ定圧で伝播す
るので、層流燃焼速度Suと火炎伝播速度Sbとの間に
次式が成立する。 Su=κSb(ρb/ρu)=κSb(TuMb)/
(TbMu) ρ:密度、T:温度、M:平均モル質量、κ:補正係数 (添字 u:未燃側、b:既燃側) Tbには断熱火炎温度、Mbには各化学種の平衡濃度か
ら得られた値をそれぞれ用い、κ=1としてSuを求め
た。テトラフルオロメタン、ブロモトリフルオロメタン
(ハロン1301)、n−C4F9COCH3、n−C5F
11COCH3を添加した場合のメタンの平均層流燃焼速
度を表2に示した。Example 2 A laminar combustion velocity was measured. For the measurement of the laminar combustion velocity, a cylindrical combustion vessel having an inner diameter of 20.0 cm and a height of 30.0 cm was used. A premixed gas (sample mixture: 9.
After charging 5% methane-0.5% additive-90.0% air; mixture temperature: room temperature; mixture pressure: 1 atm), spark ignition was performed at the center, and the flame propagation speed was measured by an ion probe. . Since the flame propagates at a substantially constant pressure in the initial stage, the following equation is established between the laminar combustion speed Su and the flame propagation speed Sb. Su = κSb (ρb / ρu) = κSb (TuMb) /
(TbMu) ρ: density, T: temperature, M: average molar mass, κ: correction coefficient (subscript u: unburned side, b: burned side) Tb is adiabatic flame temperature, Mb is equilibrium of each chemical species Using the values obtained from the concentrations, Su was determined with κ = 1. Tetrafluoromethane, bromotrifluoromethane (Halon 1301), n-C 4 F 9 COCH 3, n-C 5 F
Table 2 shows the average laminar burning velocity of methane when 11 COCH 3 was added.
【0009】[0009]
【表2】 ───────────────────────── 添加剤 平均層流燃焼速度/cm.S-1 CF4 37.2±1.7 CF3Br 22.9±1.0 n−C4F9COCH3 27.0±1.0 n−C5F11COCH3 25.0±1.0 ───────────────────────── 表2の結果より、含フッ素ケトンは臭素原子をもつハロ
ン1301に次ぐ優秀な消火性能をもつことが明らかと
なった。Table 2 添加 Additives Average laminar flow rate / cm. S -1 CF 4 37.2 ± 1.7 CF 3 Br 22.9 ± 1.0 n-C 4 F 9 COCH 3 27.0 ± 1.0 n-C 5 F 11 COCH 3 25.0 ± 1 0.0 よ り From the results in Table 2, the fluorinated ketone has the best fire-extinguishing performance next to Halon 1301 having a bromine atom. It became clear to have.
【0010】[0010]
【発明の効果】本発明の含フッ素系消火薬剤は、分子内
に水素原子及びカルボニル結合をもつために、ペルフル
オロ炭化水素よりも大気寿命が短く、またオゾン層破壊
の原因となる臭素原子を含まないために規制ハロンの代
替消火剤として好適である。また含フッ素ケトンは低表
面エネルギー性をもつので、粉末消火剤に添加すること
により、微粉末の消火薬剤の凝縮防止作用をもたせるな
どの効果も有している。The fluorine-containing fire extinguishing agent of the present invention has a shorter atmospheric life than a perfluorohydrocarbon and also contains a bromine atom which causes ozone layer destruction because it has a hydrogen atom and a carbonyl bond in the molecule. Since it is not available, it is suitable as an alternative fire extinguishing agent for regulated halon. Further, since the fluorine-containing ketone has a low surface energy property, by adding it to the powder fire extinguishing agent, it also has an effect of preventing condensation of the fine powder fire extinguishing agent.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 田窪 征司 東京都文京区本郷2−40−17本郷若井ビ ル6階 財団法人地球環境産業技術研究 機構 新規冷媒等プロジェクト室内 (72)発明者 鈴田 哲也 東京都文京区本郷2−40−17本郷若井ビ ル6階 財団法人地球環境産業技術研究 機構 新規冷媒等プロジェクト室内 (72)発明者 関屋 章 茨城県つくば市東1丁目1番 工業技術 院物質工学工業技術研究所内 審査官 伊藤 陽 (56)参考文献 特開 平4−187163(JP,A) 特開 平5−49711(JP,A) 特開 平8−24362(JP,A) 特表 平6−501629(JP,A) 特表 平6−501628(JP,A) (58)調査した分野(Int.Cl.6,DB名) A62D 1/00 ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Seiji Takubo 6th floor of Hongo Wakai Building, 2-40-17 Hongo, Bunkyo-ku, Tokyo New Refrigerant Project Room, etc. (72) Inventor Tetsuya Suzuda 6-floor Hongo Wakai Building, Hongo 2-40-17, Bunkyo-ku, Tokyo New Research Project Room for New Refrigerants, etc. (72) Inventor Akira Sekiya 1-1-1, Higashi, Tsukuba, Ibaraki Pref. Examiner in the Technical Research Institute Youto Itoh (56) References JP-A-4-187163 (JP, A) JP-A-5-49711 (JP, A) JP-A-8-24362 (JP, A) 501629 (JP, A) Table 6 6-501628 (JP, A) (58) Fields investigated (Int. Cl. 6 , DB name) A62D 1/00
Claims (2)
し、R1はメチル基又はエチル基を示す)で表される含
フッ素ケトンを主成分として用いることを特徴とする消
火薬剤。[Claim 1] The following general formula (1) (Wherein, n represents a number of 4 to 8, m represents a number of 0 or 1, and R 1 represents a methyl group or an ethyl group). And extinguishing agents.
CF2COCH3、CF3CF2CF2CF2CF2COCH3
及び(CF3)2CFCF2CF2COCH3の中から選ば
れる少なくとも1種の含フッ素ケトンである請求項1の
消火薬剤。2. The fluorinated ketone is CF 3 CF 2 CF 2
CF 2 COCH 3 , CF 3 CF 2 CF 2 CF 2 CF 2 COCH 3
And (CF 3) 2 CFCF 2 CF 2 at least one fire extinguishing agent according to claim 1 is a fluorinated ketone selected from among COCH 3.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10361198A JP2893038B1 (en) | 1998-03-31 | 1998-03-31 | Fire extinguisher |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10361198A JP2893038B1 (en) | 1998-03-31 | 1998-03-31 | Fire extinguisher |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2893038B1 true JP2893038B1 (en) | 1999-05-17 |
JPH11276634A JPH11276634A (en) | 1999-10-12 |
Family
ID=14358580
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10361198A Expired - Lifetime JP2893038B1 (en) | 1998-03-31 | 1998-03-31 | Fire extinguisher |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2893038B1 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001005468A3 (en) * | 1999-07-20 | 2002-09-12 | 3M Innovative Properties Co | Use of fluorinated ketones in fire extinguishing compositions |
WO2004014490A1 (en) * | 2002-08-07 | 2004-02-19 | Solvay Fluor Und Derivate Gmbh | Fire extinction and fire prevention method |
EP1362619A3 (en) * | 1999-07-20 | 2004-07-21 | 3M Innovative Properties Company | Fire extinguishing composition |
US6780220B2 (en) | 2000-05-04 | 2004-08-24 | 3M Innovative Properties Company | Method for generating pollution credits while processing reactive metals |
RU2809284C1 (en) * | 2023-02-17 | 2023-12-11 | Общество с ограниченной ответственностью научно-производственное объединение "ПиМ-Инвест" (ООО НПО "ПиМ-Инвест") | Method for producing polyfluoralkylmethyl ketones |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3360107B2 (en) * | 2000-03-31 | 2002-12-24 | 独立行政法人産業技術総合研究所 | Azeotropic and azeotropic compositions comprising fluorinated ketones and alcohols |
JP2009160387A (en) * | 2007-12-11 | 2009-07-23 | Vision Development Co Ltd | Microencapsulated fire extinguisher and manufacturing method thereof, and fire extinguishing composite material |
-
1998
- 1998-03-31 JP JP10361198A patent/JP2893038B1/en not_active Expired - Lifetime
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001005468A3 (en) * | 1999-07-20 | 2002-09-12 | 3M Innovative Properties Co | Use of fluorinated ketones in fire extinguishing compositions |
EP1362619A3 (en) * | 1999-07-20 | 2004-07-21 | 3M Innovative Properties Company | Fire extinguishing composition |
US6780220B2 (en) | 2000-05-04 | 2004-08-24 | 3M Innovative Properties Company | Method for generating pollution credits while processing reactive metals |
WO2004014490A1 (en) * | 2002-08-07 | 2004-02-19 | Solvay Fluor Und Derivate Gmbh | Fire extinction and fire prevention method |
RU2809284C1 (en) * | 2023-02-17 | 2023-12-11 | Общество с ограниченной ответственностью научно-производственное объединение "ПиМ-Инвест" (ООО НПО "ПиМ-Инвест") | Method for producing polyfluoralkylmethyl ketones |
Also Published As
Publication number | Publication date |
---|---|
JPH11276634A (en) | 1999-10-12 |
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