JPH01232976A - Fire extinguishant and method for using same for dangerous material difficult to extinguishment - Google Patents
Fire extinguishant and method for using same for dangerous material difficult to extinguishmentInfo
- Publication number
- JPH01232976A JPH01232976A JP5958588A JP5958588A JPH01232976A JP H01232976 A JPH01232976 A JP H01232976A JP 5958588 A JP5958588 A JP 5958588A JP 5958588 A JP5958588 A JP 5958588A JP H01232976 A JPH01232976 A JP H01232976A
- Authority
- JP
- Japan
- Prior art keywords
- component
- fire
- powder
- boron oxide
- suffocating
- 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
Links
- 238000000034 method Methods 0.000 title claims description 13
- 239000000463 material Substances 0.000 title abstract description 12
- 239000000843 powder Substances 0.000 claims abstract description 80
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 47
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 claims abstract description 33
- 229910052810 boron oxide Inorganic materials 0.000 claims abstract description 30
- 238000002844 melting Methods 0.000 claims abstract description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 26
- 230000008018 melting Effects 0.000 claims abstract description 25
- 239000007788 liquid Substances 0.000 claims abstract description 19
- 238000001816 cooling Methods 0.000 claims abstract description 15
- 230000005496 eutectics Effects 0.000 claims abstract description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 78
- 230000000694 effects Effects 0.000 claims description 38
- 239000000377 silicon dioxide Substances 0.000 claims description 30
- 239000002245 particle Substances 0.000 claims description 25
- 239000000126 substance Substances 0.000 claims description 21
- 206010003497 Asphyxia Diseases 0.000 claims description 19
- 239000011148 porous material Substances 0.000 claims description 18
- 239000000383 hazardous chemical Substances 0.000 claims description 15
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical group [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 14
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 13
- 239000004576 sand Substances 0.000 claims description 11
- 230000004888 barrier function Effects 0.000 claims description 9
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 8
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 8
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 claims description 8
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 7
- 239000010453 quartz Substances 0.000 claims description 7
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 7
- 239000011780 sodium chloride Substances 0.000 claims description 7
- 229910001634 calcium fluoride Inorganic materials 0.000 claims description 6
- 239000005995 Aluminium silicate Substances 0.000 claims description 4
- 235000012211 aluminium silicate Nutrition 0.000 claims description 4
- 229910021538 borax Inorganic materials 0.000 claims description 4
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 4
- 239000013056 hazardous product Substances 0.000 claims description 4
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 4
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 claims description 4
- 239000001095 magnesium carbonate Substances 0.000 claims description 4
- 229910000021 magnesium carbonate Inorganic materials 0.000 claims description 4
- 239000001103 potassium chloride Substances 0.000 claims description 4
- 235000011164 potassium chloride Nutrition 0.000 claims description 4
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 claims description 3
- 239000010451 perlite Substances 0.000 claims description 3
- 235000019362 perlite Nutrition 0.000 claims description 3
- 239000004328 sodium tetraborate Substances 0.000 claims description 3
- 235000010339 sodium tetraborate Nutrition 0.000 claims description 3
- 235000010216 calcium carbonate Nutrition 0.000 claims description 2
- SHFGJEQAOUMGJM-UHFFFAOYSA-N dialuminum dipotassium disodium dioxosilane iron(3+) oxocalcium oxomagnesium oxygen(2-) Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[Na+].[Na+].[Al+3].[Al+3].[K+].[K+].[Fe+3].[Fe+3].O=[Mg].O=[Ca].O=[Si]=O SHFGJEQAOUMGJM-UHFFFAOYSA-N 0.000 claims description 2
- 239000011777 magnesium Substances 0.000 description 19
- 229910052751 metal Inorganic materials 0.000 description 18
- 239000002184 metal Substances 0.000 description 18
- 238000002485 combustion reaction Methods 0.000 description 13
- 239000007787 solid Substances 0.000 description 13
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 10
- 238000005507 spraying Methods 0.000 description 10
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 8
- 229910052796 boron Inorganic materials 0.000 description 8
- 235000002639 sodium chloride Nutrition 0.000 description 8
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 7
- 239000007789 gas Substances 0.000 description 7
- 230000005484 gravity Effects 0.000 description 7
- 229910052749 magnesium Inorganic materials 0.000 description 7
- 239000005997 Calcium carbide Substances 0.000 description 6
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
- 239000010935 stainless steel Substances 0.000 description 6
- 229910001220 stainless steel Inorganic materials 0.000 description 6
- CLZWAWBPWVRRGI-UHFFFAOYSA-N tert-butyl 2-[2-[2-[2-[bis[2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl]amino]-5-bromophenoxy]ethoxy]-4-methyl-n-[2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl]anilino]acetate Chemical compound CC1=CC=C(N(CC(=O)OC(C)(C)C)CC(=O)OC(C)(C)C)C(OCCOC=2C(=CC=C(Br)C=2)N(CC(=O)OC(C)(C)C)CC(=O)OC(C)(C)C)=C1 CLZWAWBPWVRRGI-UHFFFAOYSA-N 0.000 description 6
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 125000005234 alkyl aluminium group Chemical group 0.000 description 5
- 230000004927 fusion Effects 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- 239000011593 sulfur Substances 0.000 description 5
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- 239000000155 melt Substances 0.000 description 4
- 229920004449 Halon® Polymers 0.000 description 3
- 241001085205 Prenanthella exigua Species 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 239000000292 calcium oxide Substances 0.000 description 3
- 235000012255 calcium oxide Nutrition 0.000 description 3
- 239000001569 carbon dioxide Substances 0.000 description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 description 3
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 3
- 238000004880 explosion Methods 0.000 description 3
- 150000004756 silanes Chemical class 0.000 description 3
- 229910000861 Mg alloy Inorganic materials 0.000 description 2
- VKCLPVFDVVKEKU-UHFFFAOYSA-N S=[P] Chemical compound S=[P] VKCLPVFDVVKEKU-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- -1 alkyl lithium Chemical compound 0.000 description 2
- 230000000903 blocking effect Effects 0.000 description 2
- WASQWSOJHCZDFK-UHFFFAOYSA-N diketene Chemical compound C=C1CC(=O)O1 WASQWSOJHCZDFK-UHFFFAOYSA-N 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 235000014380 magnesium carbonate Nutrition 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 239000002075 main ingredient Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 235000017550 sodium carbonate Nutrition 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- OBSZRRSYVTXPNB-UHFFFAOYSA-N tetraphosphorus Chemical compound P12P3P1P32 OBSZRRSYVTXPNB-UHFFFAOYSA-N 0.000 description 2
- 230000003313 weakening effect Effects 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 238000003723 Smelting Methods 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910000085 borane Inorganic materials 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000009970 fire resistant effect Effects 0.000 description 1
- 239000010436 fluorite Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003779 heat-resistant material Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910001562 pearlite Inorganic materials 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- ZDHXKXAHOVTTAH-UHFFFAOYSA-N trichlorosilane Chemical compound Cl[SiH](Cl)Cl ZDHXKXAHOVTTAH-UHFFFAOYSA-N 0.000 description 1
- 239000005052 trichlorosilane Substances 0.000 description 1
- UORVGPXVDQYIDP-UHFFFAOYSA-N trihydridoboron Substances B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 1
- 230000002747 voluntary effect Effects 0.000 description 1
- 229910001845 yogo sapphire Inorganic materials 0.000 description 1
Landscapes
- Fire-Extinguishing Compositions (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、難消火性危険物の消火剤及びこれを使用する
消火方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a fire extinguishing agent for difficult-to-extinguish dangerous substances and a fire extinguishing method using the same.
(従来の技術とその問題点) 難消火性危険物には大別して次のような物質がある。(Conventional technology and its problems) Dangerous substances that are difficult to extinguish are classified into the following types:
■金属粉−−−Mg粉、AI粉、Zn粉、TI粉、Zr
粉、Fe粉等
■アルカリ金属・・・Na、に、Li等■禁水物質・・
・炭化カルシウム、りん化石灰、生石灰等 。■Metal powder---Mg powder, AI powder, Zn powder, TI powder, Zr
powder, Fe powder, etc. ■Alkali metals...Na, Li, etc. ■Water-inhibited substances...
・Calcium carbide, lime phosphide, quicklime, etc.
■可燃性固体・・・赤りん、黄りん、硫黄、硫化りん、
マグネシウム等
■難消火性液体・・・アルキルアルミニウム、アルキル
リチウム、塩化シラン、
ジケテン等
まず■のMg、 AI、 TI等の金属粉は可燃性で、
しばしば火災および重大な爆発を起こすことがある。■Flammable solids: red phosphorus, yellow phosphorus, sulfur, phosphorus sulfide,
Magnesium, etc. ■ Fire-resistant liquids: alkyl aluminum, alkyl lithium, chlorinated silane, diketene, etc. First of all, metal powders such as Mg, AI, TI, etc. are flammable.
May cause fire and serious explosion.
これらの金属粉は高温において水と反応して、水素を発
生し、注水すると水蒸気爆発を起こし、燃焼金属粉を飛
散させることもあるので、注水は絶対に避けなければな
らない。従来よく使われる炭酸ガス、ハロン及び粉末消
火剤では消火が不可能で、わずかに乾燥砂や塩化ナトリ
ウム、炭酸ナトリウムのような特殊粉末を散布して火勢
を抑制する方法ぐらいしか手段がなかった。しかしこれ
らの方法では多量の消火剤を消費し、またこれらの特殊
粉末を散布しても内部には高温になった金属の燗が残り
、長時間、時として30分〜60分間もそのまま放置し
ておかなければならず、また条件によっては再燃焼する
という危険があった。These metal powders react with water at high temperatures to generate hydrogen, and when water is injected, it may cause a steam explosion and scatter the burning metal powder, so water injection must be avoided at all costs. It was impossible to extinguish the fire with the commonly used carbon dioxide gas, halon, and powder extinguishing agents, and the only way to suppress the fire was to spray dry sand, special powders such as sodium chloride, and sodium carbonate. However, these methods consume a large amount of extinguishing agent, and even after spraying these special powders, hot metal remains inside the fire, leaving the fire unattended for a long time, sometimes even for 30 to 60 minutes. There was a risk of re-combustion depending on the conditions.
つぎに■のナトリウム、カリウム等のアルカリ金属は、
水と作用して発熱し、水素を発生して自然発火する危険
性がある。したがってこの場合も注水は不可であり、し
かも水以外の公知の消火剤、炭酸ガス、ハロン及び粉末
消火剤でも消火は不可能である。わずかに乾燥砂か塩化
ナトリウム、炭酸ナトリウム等の特殊粉末を散布する方
法もあるが、これらは緩慢な窒息、冷却作用による消火
であるため、完全消火に長時間を要するばか多量の消火
剤を消費する等の難点があった。Next, the alkali metals such as sodium and potassium in ■ are
There is a risk of spontaneous combustion due to the interaction with water, which generates heat and generates hydrogen. Therefore, in this case as well, water injection is not possible, and furthermore, it is impossible to extinguish the fire with known fire extinguishing agents other than water, such as carbon dioxide gas, halon, and powder fire extinguishing agents. There is also a method of spraying a small amount of dry sand or special powder such as sodium chloride or sodium carbonate, but these methods use slow suffocation and cooling effects to extinguish the fire, so it takes a long time to completely extinguish the fire and consumes a large amount of extinguishing agent. There were some difficulties, such as:
■の炭化カルシウム、生石灰などの禁水物質の固体は水
と作用して発熱したり、可燃性ガスを発生して燃焼する
。これらのものは、禁水物質といわれる危険物であり、
また水以外の他の公知の消火剤とも反応するので適応不
可であり、とくに効果のある消火方法がなかった。僅か
に乾燥砂による窒息消火が適応可となっていたが、実際
的には多量の乾燥砂を必要とする上に中々消火が困難で
あった。Solid water-prohibiting substances such as calcium carbide and quicklime (2) interact with water to generate heat or flammable gas and burn. These substances are dangerous substances called water-restricted substances.
Furthermore, it is not applicable because it reacts with other known extinguishing agents other than water, and there has been no particularly effective extinguishing method. Suffocating fire extinguishing with dry sand was slightly applicable, but in practice it required a large amount of dry sand and was difficult to extinguish.
−■の可燃性固体である黄りん、赤りん、硫黄は比較的
低温で着火し易い危険物である。しかも燃焼速度が早い
固体であり、有毒なもの、あるいは燃焼のとき有毒ガス
を発生するものもある。そのため消火が面倒である。-■ Flammable solids such as yellow phosphorus, red phosphorus, and sulfur are dangerous substances that easily ignite at relatively low temperatures. Furthermore, they are solids that burn quickly, and some are toxic or emit toxic gases when burned. Therefore, extinguishing the fire is troublesome.
■の難消火性液体のうち、アルキルアルミニウム、塩化
シランは水と接触すると爆発的に反応するめで、これら
危険物の消火に注水は絶対に避けなければならない。ま
た炭酸ガス、ハロンや従来の粉末消火剤では消火が困難
ないし不可能であった。Among the non-extinguishing liquids listed in (2), alkyl aluminum and chlorinated silane react explosively when they come into contact with water, so it is absolutely necessary to avoid pouring water to extinguish these dangerous substances. It was also difficult or impossible to extinguish the fire with carbon dioxide, halon, or conventional powder fire extinguishers.
(問題点を解決するための手段)
本発明者は、かかる消火困難な難消火性危険物の消火に
ついて種々検討を重ねた結果、前記金属粉およびアルカ
リ金属の金属火災には、酸化はう素粉末の散布がきわめ
て効果的であり、従来の金属火災用消火剤の欠点を解消
できることを見出しこれについて特許出願したが(昭和
62年12月28日付、特願昭62−335,445)
、さらに種々検討を重ねた結果、金属以外の難消火性
危険物の消火にも酸化ホウ素粉末が適用可能であり、多
種類を対象とする難消火性危険物の消火効果が更に改善
されることを見出し、本発明を完成した。(Means for Solving the Problems) As a result of various studies on extinguishing such difficult-to-extinguish and difficult-to-extinguish dangerous materials, the present inventor found that boronic oxide He discovered that spraying powder was extremely effective and could eliminate the drawbacks of conventional extinguishing agents for metal fires, and filed a patent application for this (Patent Application No. 335,445, December 28, 1988).
Further, as a result of various studies, it was found that boron oxide powder can be applied to extinguishing difficult-to-extinguish dangerous materials other than metals, and the extinguishing effect of many kinds of difficult-to-extinguish dangerous materials can be further improved. They discovered this and completed the present invention.
すなわち本発明は、B、03含有量90重量%以上、水
分含有量2重量%以下で、かつ粒子直径5〜1000μ
mの酸化はう素粉末を主成分とし、燃焼物体に該主成分
と共融し融点を低下させて窒息、冷却作用を発揮する第
1成分、該物体上に強度の大なる窒息遮断層を形成する
第2成分および液状の該物体を吸液して除去、窒息作用
を発揮する第3成分のいずれか一種もしくはそれらの任
意組合せを副成分としてなる難消火性危険物用消火剤を
要旨とし、さらにこれを使用する消火方法に関するもの
である。That is, in the present invention, the B, 03 content is 90% by weight or more, the moisture content is 2% by weight or less, and the particle diameter is 5 to 1000μ.
The main component is boron oxide powder, which is eutectic with the main component to lower the melting point of the burning object to exert a suffocation and cooling effect, and a strong suffocation barrier layer is formed on the object. The gist is a fire extinguishing agent for refractory hazardous materials, which contains as subcomponents any one of the second component to form and a third component that absorbs and removes the liquid substance and exhibits a suffocation effect, or any combination thereof. , and further relates to a fire extinguishing method using the same.
以下本発明をさらに詳しく説明する。The present invention will be explained in more detail below.
本発明における消火剤の主成分はB2O3の含有量90
重量%以上でかつ水分含有量は2重量%以下、好ましく
は0.5重量%以下の酸化はう素であることが必要であ
る。今日市販されている酸化はう素は、試薬一級品でB
2O3の含有量85重量%、水分含有量(はう酸の形で
含有)10重量%程度であるが、この程度の品位の酸化
はう素は本発明の消火剤としては不適当である。試薬一
級品の酸化はう素をさらに精製した試薬特級量は、B2
O3含有量97重量%、水分含有量2重量%程度となる
。このような品位になると、本発明の消火剤としてなん
とか使用することが可能となるがまだ充分ではない。こ
の試薬特級量をさらに160℃で2時間程度加熱すると
水分含有量が0,5%以下となり、消火性能がいちじる
しく改善される。The main component of the fire extinguishing agent in the present invention is B2O3 content of 90
It is necessary that the oxidized boron is at least 2% by weight and has a moisture content of 2% by weight or less, preferably 0.5% by weight or less. The boronic oxide that is commercially available today is a first-class reagent and is B.
The content of 2O3 is about 85% by weight and the water content (contained in the form of ferrous acid) is about 10% by weight, but oxidized boron of this grade is inappropriate as the fire extinguishing agent of the present invention. The special grade reagent, which is further purified from the first grade reagent oxidized boron, is B2.
The O3 content is about 97% by weight and the water content is about 2% by weight. Although such a quality makes it possible to use it as a fire extinguishing agent according to the present invention, it is still not sufficient. When this special grade reagent is further heated at 160° C. for about 2 hours, the water content becomes 0.5% or less, and the fire extinguishing performance is significantly improved.
本発明で用いる酸化はう素線束の粒子径は5μm〜to
ooμmである0粒子径が5〜200μmの微粉末は消
火器への充填に通し、200〜1000μmのものは、
スコップ、バケツ等で散布するのに適している。粒子径
が5μm未満の微粉末は散布時に周囲へ飛散し易いので
本発明の難消火性危険物の消火剤としては不向きである
。また粒子径が1000μmより大きいものは、融解に
時間がかかるほか、消火に多量の粉末を消費するので好
ましくない。The particle diameter of the oxide wire bundle used in the present invention is 5 μm to
Fine powder with a particle diameter of 5 to 200 μm (ooμm) is passed through filling into a fire extinguisher, and one with a particle size of 200 to 1000 μm is
Suitable for spraying with shovels, buckets, etc. Fine powder with a particle size of less than 5 μm is unsuitable as a fire extinguisher for difficult-to-extinguish dangerous substances according to the present invention because it easily scatters to the surroundings when sprayed. Particles with a particle size larger than 1000 μm are not preferred because they take a long time to melt and require a large amount of powder to extinguish fires.
つぎに上記主成分に添加する副成分とそれらがもつ作用
を述べる。Next, the subcomponents added to the above main ingredients and their effects will be described.
(1)比較的低融点のため、酸化はう素と共融して、窒
息作用と冷却作用を発揮する第1成分。(1) The first component has a relatively low melting point and thus eutectics with boron oxide to exert suffocation and cooling effects.
:塩化ナトリウム、塩化カリウム、炭酸ナトリウム、炭
酸マグネシウム、四ほう酸ナトリウム(無水)。: Sodium chloride, potassium chloride, sodium carbonate, magnesium carbonate, sodium tetraborate (anhydrous).
(2)酸化はう素と共融して、強度の大きな空気遮断層
を形成して消火作用を完全にする第2成分。(2) A second component that is eutectic with the oxidized boron to form a strong air barrier layer and complete the fire extinguishing effect.
:けい砂、けい石粉、石英粉、弗化カルシウム(3)液
状の燃焼高温物体に対し吸液、除去作用と溶融酸化はう
素の窒息、冷却作用を併用する第3成分。: Silica sand, silica powder, quartz powder, calcium fluoride (3) A third component that has a liquid absorption and removal effect on liquid burning high-temperature substances, and a suffocation and cooling effect of molten oxidation boron.
ニジリカ系多孔質体・シリカ・アルミナ系、多孔質体、
カオリン、炭酸カルシウム、パーライト第1成分は何れ
も融点が700〜900℃の範囲で、比較的低く、燃焼
中の高温物体に触れて融解しやすく、酸化はう素と混合
していると共融点が上記融点よりも下がって、燃焼表面
をよく覆う作用を示す。またこれら成分は融解熱が比較
的大きいので、融解時に周囲から、融解熱を吸収して、
冷却効果も発揮して消火作用を行う。Rainbow silica based porous material, silica/alumina based porous material,
The melting points of kaolin, calcium carbonate, and the first component of pearlite are all in the range of 700 to 900°C, which is relatively low, and they easily melt when they come into contact with a hot object that is being burned, and when mixed with boron oxide, they reach a eutectic point. is lower than the above melting point, showing the effect of covering the burning surface well. In addition, these components have a relatively large heat of fusion, so when they melt, they absorb the heat of fusion from the surroundings,
It also has a cooling effect and extinguishes fire.
適応する難消火性危険物:金属粉、アルカリ金属、可燃
性固体、
第2成分のうちシソ左系のけい砂、けい石粉、石英粉は
いずれも5i02を主成分とし、公知のように耐熱ガラ
スの重要原料であるが、酸化はう素にこれらの粉末を添
加したものは、燃焼中の高温物体に触れてシリカの融点
(1680℃)よりも低い温度で融解して、燃焼表面に
ガラス状の強固な空気遮断層を形成し消火を確実なもの
とする作用がある。Applicable fire-retardant hazardous materials: metal powder, alkali metals, flammable solids, and among the second ingredients, silica sand, silica powder, and quartz powder all have 5i02 as their main ingredient, and heat-resistant glass as well-known When these powders are added to boronic oxide, they melt at a temperature lower than the melting point of silica (1,680°C) when they come into contact with a burning object, leaving a glassy surface on the burning surface. It has the effect of forming a strong air barrier layer and ensuring fire extinguishment.
また弗化カルシウムも耐熱性が高く、金属製錬の際の融
剤として知られ、酸化はう素と混合し溶融温度を下げる
ことができる。Calcium fluoride also has high heat resistance and is known as a fluxing agent in metal smelting, and can be mixed with boron oxide to lower the melting temperature.
適応する難消火性危険物:金属粉、マグネシウム固体、
特にタンクその他の複雑な構造物で垂直壁を有するもの
が下部から発火した場合、消火剤は低温で溶融して垂直
壁に付着し、しかも粘度が高いため強固な空気遮断層と
なって壁を覆い効果的な消火能力をもつ。したがってマ
グネシウムやマグネシウム合金を多量に使っている航空
機の立体火災の消火にきわめてすぐれた効果を発揮する
。Suitable non-extinguishable hazardous materials: metal powder, magnesium solids, especially when a tank or other complex structure with vertical walls ignites from the bottom, the extinguishing agent melts at low temperatures and adheres to the vertical walls; Due to its high viscosity, it forms a strong air barrier that covers walls and has effective fire extinguishing capabilities. Therefore, it is extremely effective in extinguishing multi-dimensional fires on aircraft that use large amounts of magnesium and magnesium alloys.
第3成分のような耐熱性の高い多孔質粉末および耐熱性
の高い微粉末は、難消火性液状危険物もしくは、低融点
可燃性固体の火災に散布すると、燃焼している液状物質
を吸収し、可燃物の除去効果が発揮される。さらに高温
度になると主成分である酸化はう素が溶融して窒息、冷
却作用が発揮される。When highly heat-resistant porous powders and heat-resistant fine powders such as the third component are sprayed on fires containing refractory liquid hazardous materials or low-melting combustible solids, they absorb the burning liquid substances. , the effect of removing combustibles is exhibited. At even higher temperatures, the main component, boron oxide, melts, causing suffocation and cooling effects.
また、水と接触して発熱発火する炭化カルシウムのよう
な禁水性危険物の火災は水分が原因となっているので、
これら多孔質粉末および耐熱性微粉末を散布すると水分
を吸収し、結果として火勢を弱める効果も発揮される。In addition, water is the cause of fires with water-resistant hazardous materials such as calcium carbide, which generate heat and ignite when it comes into contact with water.
When these porous powders and heat-resistant fine powders are sprinkled, they absorb moisture and, as a result, have the effect of weakening the fire force.
適応する難消火性危険物
■禁水物質・・・炭化カルシウム、生石灰等■可燃性固
体・・・赤りん、硫黄、硫化りん等(融点が低いので、
融けた状態で
燃焼する)
■難消火性液体・・・アルキルアルミニウム、塩化シラ
ン、ジケテン等
これら副成分粉末の具備すべき要件はつぎのとおりであ
る。Applicable fire-retardant hazardous materials ■Water-inhibited substances: calcium carbide, quicklime, etc. ■Flammable solids: red phosphorus, sulfur, phosphorus sulfide, etc. (because of their low melting point,
(Burns in a molten state) ■Refractory liquid: Alkylaluminium, chlorinated silane, diketene, etc. The requirements for these subcomponent powders are as follows.
■シリカ系多孔質体
Sin、を80重量%以上含み、細孔直径o、i〜10
0μI、嵩比重0.2〜0.5、粒子径5μ田〜100
0μmのシリカ系多孔質体。■ Contains 80% by weight or more of silica-based porous material Sin, pore diameter o, i ~ 10
0 μI, bulk specific gravity 0.2 to 0.5, particle size 5 μ to 100
Silica-based porous material with a diameter of 0 μm.
■シリカ・アルミナ系多孔質体
5in2およびAl2O3の両成分の和を90重量%以
上含み、細孔直径0.1〜1000μm、嵩比重0.3
〜0.7 、粒子径5μm〜1000μmのシリカ・ア
ルミナ系多孔質体。真珠岩から作られるパーライトもこ
れに含まれる。■Silica-alumina porous material Contains 90% or more of the sum of both components of 5in2 and Al2O3, pore diameter 0.1-1000μm, bulk specific gravity 0.3
~0.7, a silica/alumina porous material with a particle size of 5 μm to 1000 μm. This also includes perlite, which is made from nacre.
■けい砂
Sin、90重量%以上を含み、真比重2.5〜2.7
粒子径1μm〜500μmの天然けい砂及びその加工品
。■Contains silica sand Sin, 90% by weight or more, true specific gravity 2.5 to 2.7
Natural silica sand with a particle size of 1 μm to 500 μm and its processed products.
■けい石粉
5in293重量%以上を含み、真比重2.5〜2.6
55粒子径1m〜500 pmのけい石粉。■ Contains 5 inches of silica powder 293% by weight or more, true specific gravity 2.5-2.6
55 Silica powder with a particle size of 1 m to 500 pm.
■石英粉
5i0295重量%以上を含み、真比重2.6〜2.6
5粒子径1μfil〜500μmの石英粉で、石英(水
晶)を人工的に粉砕加工して得られる。■Contains 5i0295% or more of quartz powder by weight, true specific gravity 2.6-2.6
5 Quartz powder with a particle size of 1 μfil to 500 μm, obtained by artificially crushing quartz (crystal).
■カオリン
耐火度が高く、真比重2.55〜2.65、平均粒子径
0.3μm〜5μIのものが適する。(2) Kaolin having a high refractoriness, a true specific gravity of 2.55 to 2.65, and an average particle diameter of 0.3 μm to 5 μI is suitable.
■塩化ナナトリウ
ムaC1分98重量%以上で、Mg塩分を極力少なくし
て吸湿性を防ぐことが望ましく、防湿のための加工をし
て固化防止をしたものが好ましいが、有機物を添加した
ものは、本発明の用途には不適当である。粒子径は5μ
m〜500μmの範囲のものが適当である。融点は80
1℃。■ Sodium chloride aC 1 min 98% by weight or more, it is desirable to reduce Mg salt as much as possible to prevent hygroscopicity, and it is preferable to use moisture-proof processing to prevent solidification, but those with organic substances added , is unsuitable for the use of the present invention. Particle size is 5μ
A suitable range is from m to 500 μm. Melting point is 80
1℃.
■塩化カリウム
KCI分98重量%以上で、Mg塩分を極力少なくした
ものが、吸湿、固化防止の点で好ましい。又固化防止剤
を少量添加することもできる。粒子径は5μffl〜5
00μmの範囲のものが適当である。融点は776℃。(2) Potassium chloride KCI content of 98% by weight or more and Mg salt content as low as possible are preferred from the viewpoint of moisture absorption and prevention of solidification. It is also possible to add a small amount of anti-caking agent. Particle size is 5 μffl ~ 5
A value in the range of 00 μm is suitable. Melting point is 776℃.
■炭酸ナトリウム
無水物でNa2CO,分99重量%以上、粒子径5μI
11〜500μmのものが用いられる。■Sodium carbonate anhydride, Na2CO, 99% by weight or more, particle size 5μI
Those with a diameter of 11 to 500 μm are used.
[相]炭酸カルシウム
CaC05分98重量%以上、粒子径1μm〜200μ
mの範囲のものが用いられる。[Phase] Calcium carbonate CaC05 min 98% by weight or more, particle size 1 μm to 200 μm
A range of m is used.
■炭酸マグネシウム
Mg003分97重量%以上、粒子径は1μm〜200
μmの範囲ものが用いられる。■Magnesium carbonate Mg003 min 97% by weight or more, particle size 1 μm ~ 200
A range of .mu.m is used.
@弗化カルシウム
蛍石の主成分であり、CaF2分98分量8重量%以上
径1μm〜500μm1融点1360℃で極めて安定で
ある。@Calcium fluoride is the main component of fluorite, and is extremely stable with a diameter of 1 μm to 500 μm and a melting point of 1360° C., with an amount of 8% by weight or more.
@四ほう酸ナトリウム(無水)
無水物Na2B40.分99%以上、粒子径5μ■〜1
000μ国、真比重2.36、融点741℃のもの。@Sodium tetraborate (anhydrous) Anhydrous Na2B40. min.99% or more, particle size 5μ■~1
000μ country, true specific gravity 2.36, melting point 741℃.
これらは不活性で耐熱性のある粉体中の含有水分は5重
量%以下好ましくは2重量%以下であることが、本発明
の目的達成に必要な条件である。A necessary condition for achieving the object of the present invention is that the water content in these inert and heat-resistant powders is 5% by weight or less, preferably 2% by weight or less.
従来、粉末消火剤の防湿性(疎水性)付与と、流動性改
善のために用いられているシリコーン油などの表面処理
、あるいはステアリン酸マグネシウムなどの有機物の添
加は難消火性危険物の消火性能をいちじるしく阻害する
ので避けなければならない。Conventionally, surface treatments such as silicone oil, which are used to impart moisture resistance (hydrophobicity) to dry powder fire extinguishers and improve fluidity, or the addition of organic substances such as magnesium stearate, improve the fire extinguishing performance of difficult-to-extinguish hazardous materials. It must be avoided as it significantly inhibits
(作用)
一般に消火のために必要な作用効果として、(1)除去
効果(可燃物を燃焼の原系から除去する)(2)窒息効
果(酸素供給源を遮断する)(3)冷却効果(燃焼熱を
吸収冷却して着火温度以に下げて燃焼を抑制する)
(4)抑制効果(燃焼の連鎖反応を抑制阻止する)の四
つが知られている。これらの効果は単独よりもむしろ相
乗的に作用することが多い。(Function) In general, the functions and effects necessary for extinguishing a fire include (1) removal effect (removes combustible materials from the source of combustion), (2) suffocation effect (blocks off the oxygen supply source), and (3) cooling effect ( There are four known effects: (4) Suppressing effect (suppressing and preventing chain reactions of combustion). These effects often act synergistically rather than independently.
本発明による消火剤を通用する難消火性危険物のうち固
体状の燃焼部に本発明の消火剤の主成分である水分の少
ない高純度酸化はう素粉末を散布すると、燃焼している
高温の固体危険物の表面近傍で軟化が始まり(B203
の軟化温度約320℃)、粒子と粒子がたがいに付着し
始めてアイスバーン状になり、ついで融解しくB2O3
の融点は450℃で耐熱物質としては著しく低い)、粉
末はたがいに融合し、ついにガラス状となり透明化する
。しかも酸化はう素は700〜1100℃以上において
も高い粘度を保つ特異な性質があるので流れ出すような
こともなく、また水飴状であって粘着力が著しく強いの
で、燃焼部の表面を完全に覆って空気を遮断し、窒息効
果が最大限に発揮されて完全消火にいたるのである。さ
らに酸化はう素の沸点は2250℃と極めて高いので、
これら難消火性危険物の消火時に蒸気化することもない
ので、きわめて優れた消火能力を発揮する。When spraying high-purity oxidized boron powder with low water content, which is the main component of the fire extinguishing agent of the present invention, on the solid combustion part of the hard-to-extinguish dangerous materials that can be used with the fire extinguishing agent of the present invention, the high temperature of the combustion occurs. Softening begins near the surface of the solid hazardous material (B203
(softening temperature of approximately 320°C), particles begin to adhere to each other and form an ice burn shape, and then melt and form B2O3.
Its melting point is 450°C, which is extremely low for a heat-resistant material), and the powders fuse together, eventually becoming glass-like and transparent. Furthermore, boron oxide has the unique property of maintaining a high viscosity even at temperatures above 700 to 1100°C, so it does not flow out, and since it is starch syrup-like and has extremely strong adhesive strength, it completely covers the surface of the burning part. By covering the fire and blocking air, the suffocation effect is maximized and the fire is completely extinguished. Furthermore, since the boiling point of boron oxide is extremely high at 2250℃,
Since it does not vaporize when extinguishing these difficult-to-extinguish dangerous substances, it exhibits extremely excellent extinguishing ability.
金属酸化物を高温、真空又は不活性雰囲気中で還元する
ような場合を除き、これら難消火性危険物の火災は、酸
化性雰囲気(通常は空気中)で起こるので、燃焼部が著
しく高温であっても、酸化はう素が還元されて、かえっ
て高熱を発生するようなおそれはない。Fires of these refractory hazardous materials occur in oxidizing atmospheres (usually in air), unless the metal oxide is reduced at high temperatures, in vacuum, or in an inert atmosphere. Even if there is, there is no risk that the oxidized boron will be reduced and generate high heat.
また、酸化はう素の融解熱は75.7cal/gと氷の
融解熱<79.7cal/g)に匹敵するほど大きいの
で、固体の燃焼部に散布された消火剤が融解する際に、
周囲から融解熱を吸収し、大きな冷却効果があられれ、
火勢を弱める方向に作用する。In addition, the heat of fusion of boron oxide is 75.7 cal/g, which is comparable to the heat of fusion of ice (79.7 cal/g), so when the extinguishing agent sprayed on the solid combustion part melts,
It absorbs the heat of fusion from the surrounding area and has a great cooling effect.
It acts in the direction of weakening the fire force.
(実施例1)
直径30cmのステンレス製の浅い皿に、代表的な可燃
性固体危険物である赤りんおよび硫黄をそれぞれ20g
載せ、ガストーチで点火して、全体を20秒間予備燃焼
させる。この時本発明の消火剤を散布した結果を第1表
に示す。(Example 1) In a shallow stainless steel dish with a diameter of 30 cm, 20 g each of red phosphorus and sulfur, which are typical flammable solid hazardous materials, were placed.
Place it on top, ignite it with a gas torch, and let it pre-burn for 20 seconds. Table 1 shows the results of spraying the fire extinguishing agent of the present invention at this time.
赤りん、硫黄のような低融点可燃性物質は燃焼に先立ち
−たん融解し液状になってから燃焼する性質があり、水
分の少ない高純度酸化はう素に少量のシリカ系多孔質体
を添加すると、消火性能が改善され、1・0〜b
シリカ系多孔質体の代りにシリカ・アルミナ系多孔質体
を添加しても同じ効果が得られる。Low-melting combustible substances such as red phosphorus and sulfur have the property of melting and becoming liquid before burning, so a small amount of silica-based porous material is added to high-purity oxidized boron with little moisture. As a result, the fire extinguishing performance is improved, and the same effect can be obtained even if a silica/alumina porous material is added in place of the 1.0~b silica porous material.
(実施例2)
直径10cm、深さ6cmのステンレス容器に、炭化カ
ルシウム20gをとり水10a+1を加えてアセチレン
ガスを発生させて点火、予備燃焼20秒経過後に本発明
の消火剤を散布した結果を第2表に示す。(Example 2) In a stainless steel container with a diameter of 10 cm and a depth of 6 cm, 20 g of calcium carbide was taken, 10 a+1 of water was added thereto, acetylene gas was generated, ignited, and after 20 seconds of pre-combustion, the fire extinguishing agent of the present invention was sprayed. Shown in Table 2.
このように水分の少ない高純度酸化はう素の粉末に少量
のシリカ系多孔質体を添加すると消火性能が改善される
。このように多孔質粉末を併用すると炭化カルシウムの
火災の原因となっている水分を吸収し、結果として火勢
を弱め消火時間も短かくなる。In this way, when a small amount of silica-based porous material is added to high-purity borium oxide powder with low water content, the fire extinguishing performance is improved. In this way, when porous powder is used in combination, it absorbs the moisture that causes calcium carbide fires, and as a result, the fire intensity is weakened and the extinguishing time is shortened.
(実施例3)
直径30cmのステンレス製の浅い皿にMg粉末20g
を載せ、ガストーチで点火、Mg粉の全表面に火が着い
たとき、燃焼部分をかき混ぜるとMg粉は白く輝く炎を
伴い、強い熱を出しながら、激しく燃焼した。この時点
で本発明の副成分として比較的低融点の粉末(第1成分
)を低水分高純度酸化はう米粉末に添加した消火剤を散
布した結果を第3表に示す。(Example 3) 20g of Mg powder was placed in a shallow stainless steel dish with a diameter of 30cm.
When the entire surface of the Mg powder was ignited, the burning part was stirred and the Mg powder combusted violently, producing a bright white flame and emitting strong heat. At this point, a fire extinguishing agent prepared by adding a relatively low melting point powder (first component) as a subcomponent of the present invention to a low moisture, high purity oxidized rice powder was sprayed, and Table 3 shows the results.
このように高純度酸化ほう素粉末に、比較的低融点の不
活性無機物の粉末を少量添加したものは、高純度酸化ほ
う素粉末単独の場合と比較し、金属火災の燃焼部分に散
布すると更に高温部にとどまらず、半融状態となって燃
焼表面の比較的低温部にまで広がり、消火をより完全に
する。In this way, high-purity boron oxide powder with a small amount of inert inorganic powder with a relatively low melting point added has an even greater effect when sprayed on the burning part of a metal fire, compared to high-purity boron oxide powder alone. It does not remain in the high-temperature area, but becomes semi-molten and spreads to the relatively low-temperature area on the combustion surface, making the fire extinguishing more complete.
(実施例4)
直径30cmのステンレス製の浅い皿にMg粉末20g
を載せ、ガストーチで点火、Mg粉の全表面に火が着い
たとき、燃焼部分をかき混ぜるとMg粉は白く輝く炎を
伴い、強い熱を出しながら激しく燃焼した。(Example 4) 20g of Mg powder was placed in a stainless steel shallow dish with a diameter of 30cm.
When the entire surface of the Mg powder was ignited, the burning part was stirred and the Mg powder combusted violently, producing a bright white flame and producing strong heat.
この時点で本発明の副成分として、比較的高融点の不活
性、耐熱性のある粉末 (第2成分)を低水分高純度酸
化ほう素粉末に添加した消火剤を散布した結果を第4表
に示す。At this point, Table 4 shows the results of spraying a fire extinguishing agent prepared by adding an inert, heat-resistant powder with a relatively high melting point (second component) to low-moisture, high-purity boron oxide powder as a subcomponent of the present invention. Shown below.
このように酸化はう素よりもはるかに融点の高いシリカ
(融点1680℃)粉および弗化カルシウム(融点13
60℃)粉を少量添加した消火剤は金属火災の高温部に
触れると半融もしくは溶融状態となって、酸化はう素を
単独に用いた場合に較べ燃焼表面を覆うより強固な殻を
形成し、空気を完全に遮断して、容易に鎮火に至らしめ
る。In this way, silica powder (melting point 1680°C), which has a much higher melting point than boron oxide, and calcium fluoride powder (melting point 13
When a fire extinguishing agent containing a small amount of powder (60℃) comes into contact with the high temperature part of a metal fire, it becomes semi-molten or molten, forming a stronger shell covering the burning surface than when boron oxide is used alone. The fire can be extinguished easily by completely blocking air.
(実施例5)
直径10cm、深さ8cmのステンレス容器に、難消火
性液状危険物の代表的な物質アルキルアルミニウム20
m1およびトリクロロシラン50m1をそれぞれとり、
点火して30秒予備燃焼させた後、本発明の副成分であ
るシリカ系多孔質体(第3成分)を低水分高純度酸化ほ
う素粉末に添加した消火剤を散布した結果を第5表に示
す。(Example 5) In a stainless steel container with a diameter of 10 cm and a depth of 8 cm, alkyl aluminum 20, a representative material of a non-extinguishable liquid dangerous substance, was placed.
ml and 50 ml of trichlorosilane, respectively,
After igniting and pre-combusting for 30 seconds, a fire extinguishing agent prepared by adding a silica-based porous material (third component), which is a subcomponent of the present invention, to a low-moisture, high-purity boron oxide powder is shown in Table 5. Shown below.
このように難消火性の液状危険物についても、高純度酸
化ほう素粉末とシリカ系多孔質体の粉末を混合した消火
剤を散布して、消火することができる。In this way, liquid hazardous materials that are difficult to extinguish can be extinguished by spraying a fire extinguishing agent that is a mixture of high purity boron oxide powder and silica-based porous material powder.
なおアルキルアルミニウムのように燃焼熱の大きな液状
危険物の消火では、まず、シリカ系多孔質体のような不
活性固体粉末を散布して、液体を吸収させ、散布された
シリカ系多孔質体の表面が高温になった後に、低水分高
純度酸化ほう素粉末を散布して表層部に溶融酸化はう素
の空気遮断層を形成させると容易に完全鎮火させること
ができる。When extinguishing a liquid hazardous material that generates a large amount of combustion heat, such as an alkyl aluminum, first, an inert solid powder such as a porous silica material is sprayed to absorb the liquid, and then the sprayed porous silica material absorbs the liquid. After the surface reaches a high temperature, low-moisture, high-purity boron oxide powder is sprinkled on the surface to form an air-blocking layer of molten boron oxide on the surface, making it easy to completely extinguish the fire.
(実施例6)
厚さ5IllIl+、幅10cn+、高さ30cmのマ
グネシウム板を耐火れんがの側面にほぼ垂直に立てかけ
、ガストーチでマグネシウム板に点火し、マグネシウム
板の面積の約半分が激しく燃焼するようになってから消
火剤を散布した結果を第6表に示す。(Example 6) A magnesium plate with a thickness of 5IllIl+, a width of 10cn+, and a height of 30cm was placed almost vertically on the side of a refractory brick, and the magnesium plate was ignited with a gas torch so that about half of the area of the magnesium plate was combusted violently. Table 6 shows the results of spraying fire extinguishing agent after the explosion occurred.
このように、はぼ垂直な面における金属火災では、従来
法の金属火災用消火剤の粉末は殆んど燃焼面に付着する
ことなく落下してしまい、消火が不能であったのに対し
、本発明による消火剤粉末はほぼ垂直な燃焼面にも付着
し、高温部の熱によって速やかに溶融して空気遮断層を
形成し、短時間に消火することができた。In this way, when a metal fire occurs on a nearly vertical surface, the powder of the conventional metal fire extinguishing agent falls without adhering to the burning surface, making it impossible to extinguish the fire. The fire extinguishing powder according to the present invention also adhered to the almost vertical combustion surface, and was rapidly melted by the heat of the high temperature part to form an air barrier layer, thereby extinguishing the fire in a short time.
これは本発明法による消火剤の主成分である低水分高純
度酸化はう素の見掛は固有抵抗(25℃の固有抵抗2.
6x 10I6Ωcm)および粒子径が適切であるため
に、空気中での散布もしくは密閉容器から空気中への噴
射によって容易に帯電して、燃焼金属面に付着し、加え
てその低融点(450℃)のために少しの加熱によって
、溶融しガラス化するものと説明できる。しかも高純度
酸化はう素は1100℃以上の高温度においても高い粘
性を保つため、高温の燃焼金属表面(実質的には酸化物
となっている)に粘着し、消火活動中及び鎮火後に剥離
又は落下するようなことは全く認められなかった。This is due to the apparent resistivity (specific resistance at 25°C of 2.5%) of low moisture, high purity borosilicate oxide, which is the main component of the fire extinguishing agent produced by the method of the present invention.
6x 10I6Ωcm) and a suitable particle size, it easily becomes electrically charged when dispersed in the air or injected into the air from a closed container, and adheres to the burning metal surface, as well as its low melting point (450°C). It can be explained that it melts and becomes vitrified with a little heating. In addition, high-purity boron oxide maintains high viscosity even at high temperatures of 1,100°C or higher, so it sticks to the surface of hot burning metal (which is essentially an oxide) and peels off during and after fire extinguishment. Or falling was not observed at all.
本発明の消火剤は、このように優れた特性があるので、
今日マグネシウム又はマグネシウム合金を多量に使って
いる航空機の立体火災の消火にも適用することが可能で
ある。Because the fire extinguishing agent of the present invention has such excellent properties,
It can also be applied to extinguish multi-dimensional fires in aircraft, which use large amounts of magnesium or magnesium alloys today.
(実施例7)
直径50c+aのステンレス製の浅い皿に、Mg粉末1
.0 kgを広げ、ガストーチで点火、Mg粉の全表面
に火がまわったとき、全体をかき混ぜるとMg粉は、白
く輝く炎を伴ない激しく燃焼した。この時点で酸化はう
素の主成分に第2成分の副成分を添加した消火剤を充填
した携帯型消火器(20型)を用いて消火した結果と従
来法の市販の金属火災用消火剤で消火した結果を第7表
に示す。(Example 7) In a stainless steel shallow dish with a diameter of 50c+a, 1 Mg powder was added.
.. 0 kg was spread out, ignited with a gas torch, and when the entire surface of the Mg powder was ignited, the whole was stirred and the Mg powder combusted violently with a bright white flame. At this point, the fire was extinguished using a portable fire extinguisher (type 20) filled with a fire extinguishing agent consisting of the main component of boron oxide and a second component, and a conventional commercially available extinguishing agent for metal fires. Table 7 shows the results of extinguishing the fire.
また、同時に行なわれた実験で、酸化はう素単独のケー
スと比較されたが、消火に20秒を要し、天然シリカの
効果が認められた。Additionally, in a simultaneous experiment, oxidation was compared with the case of using borine alone, but it took 20 seconds to extinguish the fire, demonstrating the effectiveness of natural silica.
(発明の効果)
以上詳細に述べたように本発明によれば、(1)難消火
性危険物の火災を容易かつ速やかに抑制し、短時間に鎮
火することができる。(Effects of the Invention) As described above in detail, according to the present invention, (1) a fire of a non-extinguishable hazardous material can be easily and quickly suppressed and extinguished in a short time.
(2)従来の乾燥砂や塩化ナトリウム、炭酸ナトリウム
等の特殊粉末消火剤に比べて、粉末散布時に音や煙の発
生も殆んどなく、又臭いや粉末の周囲への飛散も皆無で
、消火活動が容易である。(2) Compared to conventional powder extinguishing agents such as dry sand, sodium chloride, and sodium carbonate, there is almost no noise or smoke when spraying the powder, and there is no odor or powder scattering to the surrounding area. Fire extinguishing activities are easy.
(3)従来の消火剤に比べて、消火効果が確実でしかも
消火剤の所要量も少なくて済む。(3) Compared to conventional extinguishing agents, the extinguishing effect is reliable and the amount of extinguishing agent required is small.
(4)本発明の消火剤は、水平面火災はもちろのこと、
垂直面火災にも卓越した効果をもつので立体的な金属火
災にも有効である。(4) The extinguishing agent of the present invention can be used not only for horizontal fires, but also for horizontal fires.
It is also effective against vertical fires, so it is also effective against three-dimensional metal fires.
(5)難消火性危険物の燃焼表面を強固な層で完全に被
覆するので、鎮火後の後処理が容易で、周囲を汚染する
こともない。(5) Since the combustion surface of refractory hazardous materials is completely covered with a strong layer, post-treatment after extinguishing the fire is easy and the surrounding area is not contaminated.
(6)本発明の消火剤粉末は、消火器に充填して使用す
ることも、また容器に収容してバケツ、スコップ等で散
布することもできる等種々の卓越した効果を有する。(6) The fire extinguishing agent powder of the present invention has various outstanding effects, such as being able to be used by filling it into a fire extinguisher, or by storing it in a container and dispersing it with a bucket, shovel, etc.
手続補正書(自発)
R消火性危険物用消火剤及びこれを使用する消火方法3
、補正をする者
事件との関係 特許出願人
名称 信越半導体株式会社
4、代理人
6、補正の内容
l) 明細書の特許請求の範囲を別紙のとおりに補正す
る。Procedural amendment (voluntary) R Extinguishing agent for extinguishing hazardous materials and extinguishing method using it 3
, Relationship with the case of the person making the amendment Name of patent applicant: Shin-Etsu Semiconductor Co., Ltd. 4, Agent 6, Contents of amendment 1) The scope of claims in the specification is amended as shown in the attached sheet.
2)明細書第6頁第13行の「酸化ホウ素」を、「酸化
はう素」と補正する。2) "Boron oxide" on page 6, line 13 of the specification is corrected to "boron oxide."
3)明細書第15頁下から第2行のr700〜1100
℃以上に」を、rlloo℃あるいはそれ以上の温度に
」と補正する。3) r700-1100 on page 15 of the specification, second line from the bottom
``Above ℃'' should be corrected to ``at a temperature of rlloo ℃ or higher.''
以上
(別紙)
特許請求の範囲
1、 B、O,含有量90重量%以上、水分含有量2
重量%以下で、かつ粒子直径5〜1000.の酸化はう
素粉末を主成分とし、燃焼物体に該主成分と共融し融点
を低下させて窒息、冷却作用を発揮する第1成分、該物
体上に強度の大なる窒息遮断層を形成する第2成分およ
び液状の該物体を吸液して除去。Above (attached sheet) Claim 1, B, O, content 90% by weight or more, water content 2
% by weight or less, and the particle diameter is 5 to 1000. The first component is oxidized boron powder, which is eutectic with the main component and lowers the melting point of the burning object to exert a suffocation and cooling effect, forming a strong suffocation barrier layer on the object. The second component and the liquid substance are absorbed and removed.
窒息作用を発揮する第3成分のいずれか一種もしくはそ
れらの任意組合せを副成分としてなる難消火性危険物用
消火剤。A fire extinguishing agent for non-extinguishable hazardous materials, which contains as a subcomponent any one of the third components that exerts a suffocation effect or any combination thereof.
2、 前記第1成分が、塩化ナトリウム、塩化カリウム
、炭酸ナトリウム、炭酸マグネシウム、四ほう酸ナトリ
ウム(無水)からなる群より選ばれる少なくとも一種で
ある請求項1記載の消火剤。2. The extinguishing agent according to claim 1, wherein the first component is at least one selected from the group consisting of sodium chloride, potassium chloride, sodium carbonate, magnesium carbonate, and sodium tetraborate (anhydrous).
3、前記第2成分が、けい砂、けい石粉、石英粉、弗化
カルシウムからなる群より選ばれる少なくとも一種であ
る請求項1記載の消火剤。3. The fire extinguisher according to claim 1, wherein the second component is at least one selected from the group consisting of silica sand, silica powder, quartz powder, and calcium fluoride.
4、前記第3成分が、シリカ系多孔質体、シリカ・アル
ミナ系多孔質体、カオリン、炭酸カルシウム、パーライ
トからなる群より選ばれる少なくとも一種である請求項
1記載の消火剤、・
5、 B、O,含有量90重量%以上、水分含有量2
重量%以下で、かつ粒子直径5〜1000.の酸化はう
素粉末を主成分とし、燃焼物体に該主成分と共融し融点
を低下させて窒息、冷却作用を発揮する第1成分、該物
体上に強度の大なる窒息遮断層を形成する第2成分およ
び液状の該物体を吸液して除去、窒息作用を発揮する第
3成分のいずれか一種もしくはそれらの任意組合せを副
成分としてなる消火剤を燃焼物体の消火に使用すること
を特徴とする芝消火性危険物の消火方法。4. The fire extinguishing agent according to claim 1, wherein the third component is at least one member selected from the group consisting of a silica-based porous material, a silica-alumina-based porous material, kaolin, calcium carbonate, and perlite. , O, content 90% by weight or more, water content 2
% by weight or less, and the particle diameter is 5 to 1000. The first component is oxidized boron powder, which is eutectic with the main component and lowers the melting point of the burning object to exert a suffocation and cooling effect, forming a strong suffocation barrier layer on the object. A fire extinguishing agent containing any one of a second component that absorbs and removes the liquid object and a third component that exerts a suffocation effect or any combination thereof as subcomponents is used to extinguish a burning object. Features: Grass extinguishing method for extinguishing hazardous materials.
6、前記燃焼物体が地面に対し急傾斜側面をもつか、ま
たは地面に対峙する底面を有する請求項5記載の消火方
法。6. The fire extinguishing method according to claim 5, wherein the combustion object has a side surface steeply inclined to the ground or a bottom surface facing the ground.
Claims (1)
重量%以下で、かつ粒子直径5〜1000μの酸化ほう
素粉末を主成分とし、燃焼物体に該主成分と共融し融点
を低下させて窒息、冷却作用を発揮する第1成分、該物
体上に強度の大なる窒息遮断層を形成する第2成分およ
び液状の該物体を吸液して除去、窒息作用を発揮する第
3成分のいずれか一種もしくはそれらの任意組合せを副
成分としてなる難消火性危険物用消火剤。 2、前記第1成分が、塩化ナトリウム、塩化カリウム、
炭酸ナトリウム、炭酸マグネシウム、四ほう酸ナトリウ
ム(無水)からなる群より選ばれる少なくとも一種であ
る請求項1記載の消火剤。 3、前記第2成分が、けい砂、けい石粉、石英粉、弗化
カルシウムからなる群より選ばれる少なくとも一種であ
る請求項1記載の消火剤。 4、前記第3成分が、シリカ系多孔質体、シリカ・アル
ミナ系多孔質体、カオリン、炭酸カルシウム、パーライ
トからなる群より選ばれる少なくとも一種である請求項
1記載の消火剤。 5、B_2O_3含有量90重量%以上、水分含有量2
重量%以下で、かつ粒子直径5〜1000μmの酸化ほ
う素粉末を主成分とし、燃焼物体に該主成分と共融し融
点を低下させて窒息、冷却作用を発揮する第1成分、該
物体上に強度の大なる窒息遮断層を形成する第2成分お
よび液状の該物体を吸液して除去、窒息作用を発揮する
第3成分のいずれか一種もしくはそれらの任意組合せを
副成分としてなる消火剤を燃焼する燃焼物体の消火に使
用することを特徴とする難消火性危険物の消火方法。 6、燃焼物体が地面に対し急傾斜側面をもつか、または
地面に対峙する底面を有する請求項1記の消火方法。[Claims] 1. B_2O_3 content 90% by weight or more, water content 2
A first component which contains boron oxide powder as a main component and has a particle diameter of 5 to 1000 μm and which is eutectic with the main component and lowers the melting point of the burning object to exert a suffocating and cooling effect on the object; a second component that forms a strong suffocation barrier layer on the body, and a third component that absorbs and removes the liquid substance and exerts a suffocation effect, or any combination thereof as subcomponents. Extinguishing agent for hazardous materials. 2. The first component is sodium chloride, potassium chloride,
The extinguishing agent according to claim 1, which is at least one selected from the group consisting of sodium carbonate, magnesium carbonate, and sodium tetraborate (anhydrous). 3. The fire extinguisher according to claim 1, wherein the second component is at least one selected from the group consisting of silica sand, silica powder, quartz powder, and calcium fluoride. 4. The extinguishing agent according to claim 1, wherein the third component is at least one selected from the group consisting of a silica-based porous material, a silica-alumina-based porous material, kaolin, calcium carbonate, and perlite. 5, B_2O_3 content 90% by weight or more, moisture content 2
A first component whose main component is boron oxide powder with a particle diameter of 5 to 1000 μm and which is eutectic with the main component and lowers the melting point of the burning object to exert a suffocating and cooling effect on the object; A fire extinguishing agent comprising as subcomponents any one or any combination thereof, a second component that forms a strong suffocation barrier layer on the body, and a third component that absorbs and removes the liquid object and exerts a suffocation effect. A method for extinguishing a hazardous material that is difficult to extinguish and is characterized by being used to extinguish a combustible object that burns. 6. The fire extinguishing method according to claim 1, wherein the burning object has side surfaces steeply inclined to the ground or a bottom surface facing the ground.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5958588A JPH062168B2 (en) | 1988-03-14 | 1988-03-14 | Fire-extinguishing agent for fire-retardant hazardous materials and fire-extinguishing method using the same |
DE88403337T DE3885078T2 (en) | 1987-12-28 | 1988-12-27 | Process for fire extinguishing dangerous substances that are difficult to extinguish. |
EP88403337A EP0323350B1 (en) | 1987-12-28 | 1988-12-27 | Method for fire extinguishment of hardly extinguishable dangerous material |
US07/291,046 US4915853A (en) | 1987-12-28 | 1988-12-28 | Method for fire extinguishment of hardly extinguishable dangerous material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5958588A JPH062168B2 (en) | 1988-03-14 | 1988-03-14 | Fire-extinguishing agent for fire-retardant hazardous materials and fire-extinguishing method using the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01232976A true JPH01232976A (en) | 1989-09-18 |
JPH062168B2 JPH062168B2 (en) | 1994-01-12 |
Family
ID=13117453
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5958588A Expired - Lifetime JPH062168B2 (en) | 1987-12-28 | 1988-03-14 | Fire-extinguishing agent for fire-retardant hazardous materials and fire-extinguishing method using the same |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH062168B2 (en) |
Cited By (1)
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CN116421922A (en) * | 2023-03-21 | 2023-07-14 | 连云港贺尔文科技材料有限公司 | Solid extinguishing agent for spontaneous combustion coal seam or oil field and preparation method thereof |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102018008491A1 (en) * | 2018-10-30 | 2020-04-30 | Franz Wilhelm Cremer | Protective agents for electrochemical energy stores, in particular for energy stores that contain lithium |
-
1988
- 1988-03-14 JP JP5958588A patent/JPH062168B2/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116421922A (en) * | 2023-03-21 | 2023-07-14 | 连云港贺尔文科技材料有限公司 | Solid extinguishing agent for spontaneous combustion coal seam or oil field and preparation method thereof |
CN116421922B (en) * | 2023-03-21 | 2024-04-26 | 连云港贺尔文科技材料有限公司 | Solid extinguishing agent for spontaneous combustion coal seam or oil field and preparation method thereof |
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Publication number | Publication date |
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JPH062168B2 (en) | 1994-01-12 |
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