CA2348644A1 - Fire extinguishing aerosol forming means - Google Patents
Fire extinguishing aerosol forming means Download PDFInfo
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- CA2348644A1 CA2348644A1 CA002348644A CA2348644A CA2348644A1 CA 2348644 A1 CA2348644 A1 CA 2348644A1 CA 002348644 A CA002348644 A CA 002348644A CA 2348644 A CA2348644 A CA 2348644A CA 2348644 A1 CA2348644 A1 CA 2348644A1
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- burning
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- feafm
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- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D1/00—Fire-extinguishing compositions; Use of chemical substances in extinguishing fires
- A62D1/06—Fire-extinguishing compositions; Use of chemical substances in extinguishing fires containing gas-producing, chemically-reactive components
Abstract
The fire extinguishing aerosol forming means includes a flame suppressing agent, a fuel-binder, a source of carbon, a stabilizer, a modifier of burning and technological additives, it contains as the flame suppressing agent nitrates or alkaline metals or mixture thereof with complex compositions of alkaline metals, as the source of carbon - carbon as such, aliphatic or aromatic alcohols, or mixture thereof, as the modifier of burning it additionally contains a cooling agent, and as the technological additives it additionally contains compositions chosen from the class of glycoles or glycerin. As the cooling agent there could be used either individual substances, or a composition including a heat absorbing component, binding and additives. All fire extinguishing devices using the proposed agent can work in automatic and manual-operated modes, are designed for long service life (up to 10 years and longer), do not require additional service, are always ready for use and for wide purposes.
Description
Fire extinguishing aerosol forming means Summary of the invention The present invention relates to the field of extinguishing a fire, in particular, to a fire extinguishing aerosol forming means (FEAFM).
Fire extinguishing aerosol forming means have presently wide application as an effective volumetric fire extinguishing means because they are characterized by fast emitting of the fire extinguishing aerosol and fast filling the protected volume therewith, entering even into difficult places, in result the fire will be practically instantly liquidated (PCT/RU 93/00025 of Jan. 28,1993, A
62D 1/00; EP 0560095 of Jan. 25,1995, A 62D 1/00).
Extinguishing a fire with use of FEAFM is based on a principally new mechanism consisting in burning of the means with formation of gaseous and highly dispersed condensed products having inhibiting properties and suppressing the chain reaction of burning and, as result, extinguishing the flame. Aerosol formed at burning of such means has fire extinguishing properties due to the presence of alkaline metals ions therein. Potassium nitrate or a mixture thereof with potassium perchlorate is most frequently used as a source of alkaline metals ions in FEAFM. For the rest, the known FEAFM differ, as a rule, by type of binder and contain of additives of various purpose (Patents RU No.2105581 A 62C 3/00 and No.2091106 A 62D
1/00).
Variety of types of fire dangerous materials and objects, their dimensions, degree of uptightness and other features of the protected volumes dictate variety of aerosol fire extinguishing devices and as a consequence of this, large enough variety of FEAFM having a set of certain properties which could be relate to the following:
- high fire extinguishing efficiency, that could be expressed in low FEAFM fire extinguishing concentration;
- absence of negative influence on the atmosphere ozone layer and environment, i.e. ecological cleanliness of FEAFM combustion products, their low toxicity;
- reduced temperature of FEAFM combustion products;
- possibility of wide range regulation of burning. speed, i.e. speed of emitting of the fire extinguishing aerosol;
- acceptable operational characteristics (mechanical reliability, thermal-resistance, safety etc.).
The practical application conditions of FEAFM in fire extinguishing devices set forward contradictory requirements to parameters of aerosol forming: fire extinguishing efficiency and aerosol forming speed should be rather high, and temperature of the fire extinguishing aerosol should be low. In practice, high speed of aerosol forming corresponds to increased temperature of the aerosol, and significant reduction of the aerosol temperature results in loss in fire extinguishing efficiency thereof.
As the majority of FEAFM in industrial application have high temperature of burning and, hence, form a high-temperature aerosol, reduction of temperature of FEAFM
combustion products, alongside with increasing of efficiency thereof, with the purpose of creation an economic and highly effective aerosol forming firs extinguishing devices is an actual problem.
Closest to the claimed technical decision is aerosol forming fire extinguishing composition described in the Patent of the Russian Federation No.2091106, A 62D 1/00, comprising the following components, in mass ~:
potassium nitrate 45.0 - 75.0;
carbon 4.0 -.11.0;
centralyte and/or diphenylamine 0.5 - 2.0;
industrial or instrumental oil 0.5 - 2.5;
zinc and/or sodium stearate, or mixture thereof with sulforicinate and gelatin 0.02-0.5;
burning catalyst and/or inhibitor 0.5 - 20.0;
plasticized derivative of cellulose, or mixture thereof with additional binder the rest As the burning catalyst FEAFM comprises compounds chosen from the sequence including oxides of metals of variable valence or metals of the II group (oxides of iron, copper, nickel, cobalt, manganese, chrome and zinc, or mixture thereof), their organic or inorganic compositions or mixture thereof (salicylates, phthalates, acetylacetolates or oxalates of copper, nickel, cobalt, iron, manganese, zinc or calcium; carbonates of. these metals, except calcium carbonate).
As the burning inhibitor FEAFM comprises compounds chosen from the sequence including inorganic and organic phosphor containing compounds, inorganic and organic nitrogen containing compounds, hydraxides, carbonates, basic carbonates, borates of metals or trioxide of aluminum and/or mixtures thereof.
Introduction in FwAFM inhibitor or a mixture thereof with catalyst even in maximum quantity does not provide stability of the process conversion flame burning of FEAFM
in flameless gasification.
With increasing of FEAFM weight or obstruction of heat removal the process of flameless gasification changes over in flame burning again, that restricts application of FF.AFM
in fire extinguishing devices.
The modern fire extinguishing means based on use of aerosol forming compositions provide, as a rule, presence of various agents ensuring cooling of the fire extinguishing aerosol: cooling liquids (water, water solutions of salts), air ejectors, chemical thermally decomposing powders or compositions.
In the Patent of the Russian Federation No.2086278 A
62D 1/00 it is described a composition for cooling of the fire extinguishing aerosol, containing as a binder cellulose nitrate, plasticized by a low-volatile plasticizer, diphenylamine, polyvinyl acetate, carbon, iron oxide, as a filler basic manganese carbonate, or ammonium oxalate, or basic magnesium phosphate; and technological additives: industrial or instrumental ail, sodium or zinc stearate, graphite, paraffin and water at the following contents of the components, mass $:
Fire extinguishing aerosol forming means have presently wide application as an effective volumetric fire extinguishing means because they are characterized by fast emitting of the fire extinguishing aerosol and fast filling the protected volume therewith, entering even into difficult places, in result the fire will be practically instantly liquidated (PCT/RU 93/00025 of Jan. 28,1993, A
62D 1/00; EP 0560095 of Jan. 25,1995, A 62D 1/00).
Extinguishing a fire with use of FEAFM is based on a principally new mechanism consisting in burning of the means with formation of gaseous and highly dispersed condensed products having inhibiting properties and suppressing the chain reaction of burning and, as result, extinguishing the flame. Aerosol formed at burning of such means has fire extinguishing properties due to the presence of alkaline metals ions therein. Potassium nitrate or a mixture thereof with potassium perchlorate is most frequently used as a source of alkaline metals ions in FEAFM. For the rest, the known FEAFM differ, as a rule, by type of binder and contain of additives of various purpose (Patents RU No.2105581 A 62C 3/00 and No.2091106 A 62D
1/00).
Variety of types of fire dangerous materials and objects, their dimensions, degree of uptightness and other features of the protected volumes dictate variety of aerosol fire extinguishing devices and as a consequence of this, large enough variety of FEAFM having a set of certain properties which could be relate to the following:
- high fire extinguishing efficiency, that could be expressed in low FEAFM fire extinguishing concentration;
- absence of negative influence on the atmosphere ozone layer and environment, i.e. ecological cleanliness of FEAFM combustion products, their low toxicity;
- reduced temperature of FEAFM combustion products;
- possibility of wide range regulation of burning. speed, i.e. speed of emitting of the fire extinguishing aerosol;
- acceptable operational characteristics (mechanical reliability, thermal-resistance, safety etc.).
The practical application conditions of FEAFM in fire extinguishing devices set forward contradictory requirements to parameters of aerosol forming: fire extinguishing efficiency and aerosol forming speed should be rather high, and temperature of the fire extinguishing aerosol should be low. In practice, high speed of aerosol forming corresponds to increased temperature of the aerosol, and significant reduction of the aerosol temperature results in loss in fire extinguishing efficiency thereof.
As the majority of FEAFM in industrial application have high temperature of burning and, hence, form a high-temperature aerosol, reduction of temperature of FEAFM
combustion products, alongside with increasing of efficiency thereof, with the purpose of creation an economic and highly effective aerosol forming firs extinguishing devices is an actual problem.
Closest to the claimed technical decision is aerosol forming fire extinguishing composition described in the Patent of the Russian Federation No.2091106, A 62D 1/00, comprising the following components, in mass ~:
potassium nitrate 45.0 - 75.0;
carbon 4.0 -.11.0;
centralyte and/or diphenylamine 0.5 - 2.0;
industrial or instrumental oil 0.5 - 2.5;
zinc and/or sodium stearate, or mixture thereof with sulforicinate and gelatin 0.02-0.5;
burning catalyst and/or inhibitor 0.5 - 20.0;
plasticized derivative of cellulose, or mixture thereof with additional binder the rest As the burning catalyst FEAFM comprises compounds chosen from the sequence including oxides of metals of variable valence or metals of the II group (oxides of iron, copper, nickel, cobalt, manganese, chrome and zinc, or mixture thereof), their organic or inorganic compositions or mixture thereof (salicylates, phthalates, acetylacetolates or oxalates of copper, nickel, cobalt, iron, manganese, zinc or calcium; carbonates of. these metals, except calcium carbonate).
As the burning inhibitor FEAFM comprises compounds chosen from the sequence including inorganic and organic phosphor containing compounds, inorganic and organic nitrogen containing compounds, hydraxides, carbonates, basic carbonates, borates of metals or trioxide of aluminum and/or mixtures thereof.
Introduction in FwAFM inhibitor or a mixture thereof with catalyst even in maximum quantity does not provide stability of the process conversion flame burning of FEAFM
in flameless gasification.
With increasing of FEAFM weight or obstruction of heat removal the process of flameless gasification changes over in flame burning again, that restricts application of FF.AFM
in fire extinguishing devices.
The modern fire extinguishing means based on use of aerosol forming compositions provide, as a rule, presence of various agents ensuring cooling of the fire extinguishing aerosol: cooling liquids (water, water solutions of salts), air ejectors, chemical thermally decomposing powders or compositions.
In the Patent of the Russian Federation No.2086278 A
62D 1/00 it is described a composition for cooling of the fire extinguishing aerosol, containing as a binder cellulose nitrate, plasticized by a low-volatile plasticizer, diphenylamine, polyvinyl acetate, carbon, iron oxide, as a filler basic manganese carbonate, or ammonium oxalate, or basic magnesium phosphate; and technological additives: industrial or instrumental ail, sodium or zinc stearate, graphite, paraffin and water at the following contents of the components, mass $:
.
cellulose nitrate ~ 5.0 - 12.5;
low-volatile plasticizer 5.0 - 12,5;
diphenyl amine 0.1 - 0.5;
polyvinyl acetate 0.2 - 1,5;
carbon 0.1 - 0.5;
iron oxide 0.3 -~2.5;
basic manganese carbonate of ammonium oxalate or basic magnesium phosphate 25.0 - 45.0;
industrial or instrumental oil 0.5 - 5.0;
sodium or zinc stearate 0.1 - 3.0;
graphite 0.1 - 1.5;
paraffin 0.1 - 1.5;
water the rest.
This composition for cooling of aerosol is insufficiently effective because of low contents of the heat absorbing component (25-45 weight %). Furthermore, rheological, physical and mechanical properties. of the composition limit the forms of joint application thereof directly with aerosol forming compositions.
It is proposed a fire extinguishirig aerosol forming means including flame suppressing agent, fuel-binder, source of carbon, stabilizer, modifier of burning and technological additives, and as the flame suppressing agent it contains nitrates of alkaline metals or mixture thereof with complex compositions of alkaline metals, as the source of carbon - carbon as it or aliphatic or aromatic alcohols, or mixture thereof, as the modifier of burning it additionally contains a cooling agent, and as the technological additives it additionally contains compositions chosen from the class of glycoles or glycerin.
cellulose nitrate ~ 5.0 - 12.5;
low-volatile plasticizer 5.0 - 12,5;
diphenyl amine 0.1 - 0.5;
polyvinyl acetate 0.2 - 1,5;
carbon 0.1 - 0.5;
iron oxide 0.3 -~2.5;
basic manganese carbonate of ammonium oxalate or basic magnesium phosphate 25.0 - 45.0;
industrial or instrumental oil 0.5 - 5.0;
sodium or zinc stearate 0.1 - 3.0;
graphite 0.1 - 1.5;
paraffin 0.1 - 1.5;
water the rest.
This composition for cooling of aerosol is insufficiently effective because of low contents of the heat absorbing component (25-45 weight %). Furthermore, rheological, physical and mechanical properties. of the composition limit the forms of joint application thereof directly with aerosol forming compositions.
It is proposed a fire extinguishirig aerosol forming means including flame suppressing agent, fuel-binder, source of carbon, stabilizer, modifier of burning and technological additives, and as the flame suppressing agent it contains nitrates of alkaline metals or mixture thereof with complex compositions of alkaline metals, as the source of carbon - carbon as it or aliphatic or aromatic alcohols, or mixture thereof, as the modifier of burning it additionally contains a cooling agent, and as the technological additives it additionally contains compositions chosen from the class of glycoles or glycerin.
Main ingredients of the means are contained therein in the following ratio, mass parts:
flame suppressing agent 35 - 80;
fuel-binder 12 - 40;
source of carbon 3. - 15;
stabilizer 0.5 - 2,5;
modifier of burning 1 - 250;
technological additives 0.5 - 7.5.
Nitrates of alkaline metals or mixture thereof with complex compositions of alkaline metals are used as the flame suppressing agent.
The included in the structure complex compositions of alkaline metals comprise compositions having temperature of chemolysis of approximately 200pC, that is commensurable with the surface temperature of burning FEAFM. As these compositions it is preferable to use potassium or sodium dipyrocatechol, potassium hexanitrocobaltate, potassium ferrocyanide or potassium ferricyanide, or mixture thereof.
Products formed at decomposition of the complexes have superfluous energy and are active accelerators of reactions taking place in the surface layer -of FEAFM. This results in increasing of completeness of potassium nitrate decomposition. The products of chemolysis of the complex compositions of alkaline metals are also capable to break off the chain reactions of oxidation at burning process and, together with decomposition products of potassium nitrate, form a mixture effectively inhibiting process of burning.
Furthermore, using of complex compositions of alkaline metals allows to reduce essentially the lower limit of carbon contents in FEAFM, providing thus reduction of carbon monoxide contents in the products of FE_~FM
flame suppressing agent 35 - 80;
fuel-binder 12 - 40;
source of carbon 3. - 15;
stabilizer 0.5 - 2,5;
modifier of burning 1 - 250;
technological additives 0.5 - 7.5.
Nitrates of alkaline metals or mixture thereof with complex compositions of alkaline metals are used as the flame suppressing agent.
The included in the structure complex compositions of alkaline metals comprise compositions having temperature of chemolysis of approximately 200pC, that is commensurable with the surface temperature of burning FEAFM. As these compositions it is preferable to use potassium or sodium dipyrocatechol, potassium hexanitrocobaltate, potassium ferrocyanide or potassium ferricyanide, or mixture thereof.
Products formed at decomposition of the complexes have superfluous energy and are active accelerators of reactions taking place in the surface layer -of FEAFM. This results in increasing of completeness of potassium nitrate decomposition. The products of chemolysis of the complex compositions of alkaline metals are also capable to break off the chain reactions of oxidation at burning process and, together with decomposition products of potassium nitrate, form a mixture effectively inhibiting process of burning.
Furthermore, using of complex compositions of alkaline metals allows to reduce essentially the lower limit of carbon contents in FEAFM, providing thus reduction of carbon monoxide contents in the products of FE_~FM
combustion, that, in turn, leads to decreasing toxicity of the fire extinguishing aerosol itself.
Plasticized derivatives of cellulose or mixture thereof with other binder is used as a fuel-binder. It is preferred to use such compositions, as cellulose ethers, e.g.
nitrocellulose, cellulose methyl-, ethylacetates or mixtures thereof.
As plasticizers of cellulose derivatives there are used ethers of carboxylic or mineral acids and alcohols, e.g., triacetin, diethylene glycol propionate, triethylene glycol dipropionate, dibutyl phthalate, dioctyl sebacate, diethylene glycol dinitrate or triethylene glycol dinitrate or mixture thereo=.
rFEAFM can contain polyvinyl acetate, or polyvinyl alcohol, or mixture thereof as an additional binder.
As a source of carbon the means contains carbon as such, aliphatic or aromatic alcohols (e. g., sorbitol, xylitol, pirocathechol, hydroquinone or a-naphthol) or mixture thereof.
Centralyte and/or diphenylamine are mostly used as a stabilizer.
The means contains a catalyst and/or an inhibitor of burning, and a cooling agent as a modifier of burning. It is desirable for regulation of FEAFM burning characteristics to the required level.
The catalysts of burning are used for increasing of Spec''d of burning and maintenance oL burning stability at low pressure. The catalysts accelerate achievement of thermodynamic balance of oxidation reactions, those as 2N0 + 2C0 =2COz + Nz; C + 2N0 =C02 + NZ; CO + HZO =COZ + H2;
etc.
Plasticized derivatives of cellulose or mixture thereof with other binder is used as a fuel-binder. It is preferred to use such compositions, as cellulose ethers, e.g.
nitrocellulose, cellulose methyl-, ethylacetates or mixtures thereof.
As plasticizers of cellulose derivatives there are used ethers of carboxylic or mineral acids and alcohols, e.g., triacetin, diethylene glycol propionate, triethylene glycol dipropionate, dibutyl phthalate, dioctyl sebacate, diethylene glycol dinitrate or triethylene glycol dinitrate or mixture thereo=.
rFEAFM can contain polyvinyl acetate, or polyvinyl alcohol, or mixture thereof as an additional binder.
As a source of carbon the means contains carbon as such, aliphatic or aromatic alcohols (e. g., sorbitol, xylitol, pirocathechol, hydroquinone or a-naphthol) or mixture thereof.
Centralyte and/or diphenylamine are mostly used as a stabilizer.
The means contains a catalyst and/or an inhibitor of burning, and a cooling agent as a modifier of burning. It is desirable for regulation of FEAFM burning characteristics to the required level.
The catalysts of burning are used for increasing of Spec''d of burning and maintenance oL burning stability at low pressure. The catalysts accelerate achievement of thermodynamic balance of oxidation reactions, those as 2N0 + 2C0 =2COz + Nz; C + 2N0 =C02 + NZ; CO + HZO =COZ + H2;
etc.
resulting in increasing of proportion of products of complete oxidation in FEAFM burning praducts and decreasing of contents of toxic substances, in particular, carbon and nitrogen monoxides.
As the catalyst, as a rule, there used compositions of metals of variable valence, e.g., oxides of iron, copper, nickel, cobalt, manganese, chrome; organic or inorganic compositions of same metals or mixtures thereof. The catalysts are added in FEAFM in quantity from 0.5 ~to 10 mass parts, preferably 1-5 mass parts.
Inhibitors of burning are added in FEAFM for reduction oz their speed of burning, decreasing of temperature of surface burning and flame zone. Damping of chemical reactions of burning is achieved either due to blocking the active centers of flame (gas) reactions by inhibitors or products of their decomposition, or due to intensification of reactions of carbonization, resulting in forming on the surface of burning of dense and hard carbon carcass changing conditions of mass- and heat exchange on the border of gaseous and condensed phases. Due to the reaction 2n CO = Cn + n COz contents of the toxic monoxide in gaseous products is decreased.
It is reasonable to use as the inhibitor of burning compositions chosen from classes: inorganic and organic phosphor- and/or nitrogen- containing composition, borates or carbonates of metals or hydroxides of metals of the III
group or mixtures thereof.
E.g., from phosphor- and nitrogen- containing inhibitors it is preferable to use phosphates of potassium, calcium, iron of any degree of displacement; triphenyl phosphate; ammonium phosphates, ferric-ammonium phosphate, ammonium oxalate, ferric-ammonium oxalate; amides-carbamide, triazine and its derivatives, dicyanamide; among borates of metals - borates of potassium, sodium, calcium, magnesium, barium, zinc.
Quantity of entered inhibitor comprises 5-30 mass parts, preferably 15-25 mass parts.
The cooling agents are added in FEAFM for change of its thermal balance of burning. Additional reduction of temperature on the surface, and cooling of products of burning of FEAFM occurs due to physical removing of heat which is spent on heating of particles of the entered cooling agent, its endothermic decomposition, and also due to shielding of the thermal flow directed from the zone of flame reactions to the burning surface.
As the cooling agent there are used oxides and hydroxides of metals of the II group, aluminosilicates, nepheline, metal shavings or mixtures thereof, or a heat-absorbing composition.
Incombustible products of disintegration of the composition dilute products of FEAFM burning in the flame zone of reaction, reduce temperature of the flame and with it decrease return thermal flow to the surface of burning.
Interaction of FEAFM combustion products with products of disintegration of the heat-absorbing composition results in "freezing" thereof, possibility of their further interaction is eliminated, in result, it is generated a cooled aerosol. Heat-absorbing composition includes the following ingredients, mass parts:
heat-absorbing component 50-80 binder 10-35, additives 1-7, thus, as the heat-absorbing component there are mainly used carbonates or basic carbonates, phosphates of metals of the II group; crystal hydrides thereof, hydroxides of metals of the III group or mixtures thereof; as the binder -derivatives of cellulose, e.g., nitrocellulose, plasticized by a low-volatile plasticizes , e.g., triacetin and/or dibutil phthalate, and polyvinyl acetate or polyvinyl a alcohol; as the additive it is used lubricant oil, potassium or zinc stearate, organosilicon compositions and oleic acid.
Depending on the purpose and application of FEAFM in a particular fire extinguishing device, quantity of the cooling agent can vary over a wide range from 0.5 to 250 mass harts.
Lubricant oil, composition chosen from the class of glycoles, or glycerin, salt of a fatty acid, e.g., potassium or zinc stearate or mixture thereof with sulforicinate and gelatin are used in F1;AFM as the technological additives.
Introduction in F>;AFM of compositions from the class of glycoles such as diethylene glycol, triethylene glycol, or glycerin is caused by their lubricating action. Therefore they are used in quantities from 0.1 to 2 mass parts as additional technological additives lowering external friction and the phenomenon of sticking to the technological equipment during manufacturing of FEAFM and processing thereof in various products (aerosol forming elements). The best efficiency is shown with the technological additive including a triple mixture of:
lubricant oil, diethylene glycol (triethylene glycol or glycerin) and a salt of a fatty acid.
Diethylene glycol or triethylene glycol serves simultaneously as a plasticizes for cellulose derivatives, in particular, for nitrocellulose, and as an additive in _ small quantities (2-5 mass parts) to the base plasticizer it improves process of plasticization of nitrocellulose.
Manufacturing of FEAFM is carried out by mixing of all components in required proportions in an apparatus having an agitator using a dry method or in water environment (for water insoluble nitrate plasticizers) at temperature 10-55°C with subsequent forming from the received mixture of elements of necessary sizes and configuration at temperature 50-80°C. In case of in-water manufacturing of FEAFM the fire extinguishing agent is added to the mixture pressed out of water. In case of using as the cooling agent of heat-absorbing composition manufacturing thereof and forming of dements is carried out by the same way; in this case F~ArM is produced without cooling agent, and then it is performed mixing thereof or elements are used in layers.
The main characteristic of FEAFM is its fire extinguishing efficiency (FEE), i.e. minimal weight of rFEAFM, ensuring suppression of the fire in 1 m3 of protected volume.
FEE of FEAFM compositions was extensively examined in laboratory and testing stand conditions at suppression of inflammable liquids (acetone, petrol, ethyl and isopropyl alcohols, mixture of diesel fuel wit.h~ petrol) and was confirmed by tests of aerosol generators on their basis.
Laboratory technique of FEE estimation consist in following. In an exhaust hood under a glass cap of 10 1 capacity there was placed a burning alcohol-lamp or a melting-pot with inflammable liquid and a certain weight Sample Of FEAFM, connected with a Nichrome spiral. Using electric current with about 12 V voltage supplied to the Nichrome spiral it was set fire the sample of FEAFM and the process of suppression of the flame of the alcohol-limp (or inflammable liquid) was observed through the transparent glass of the cap. The result was considered to be positive if the flame was suppressed during period no longer than 5 s after burning away the sample of FEAFM. Minimal fire extinguishing concentration was determined by interpolation on two nearest points. For comparison it was carried out a check experiment on burning an alcohol-lamp (or inflammable liquid in a melting-pot) under the closed cap. Time of natural dying of the alcohol-lamp flame, due to consumption of oxygen of air enclosed under the cap, was 75 s.
American Standard UL 1058 was laid in base of testing stand technique of examination of FEAFM fire extinguishing efficiency.
In a chamber of 1 m3 volume (2.08 x 0.8 x 0.6) , having a flat screen of 0.25 m width in the middle part on whole height of the chamber, there were placed 5 sources of inflammable liauid (capacities of 75 mm in diameter, 125 mm in height with 500 ml of petrol in each of them), which were placed on four corners of the chamber and one source was placed behind the screen. Above each source of inflammable liquid in the cover of chamber there were formed small windows made of organic glass for visual observation for suppression of the fire.
The tested sample of FEAFM was placed in a metal housing and was fixed in the central part of the side wall of the chamber. Initiation of ignition of the FEAFM sample was performed using a fuse or a source of electric current located outside of the testing chamber. Petrol or another inflammable liquid in capacities was ignited, the cover of testing chamber was closed. After steady burning of inflammable liquid during 30 s it was initiated ignition of the FEAFM sample. And after 1 more minute the cover of chamber was opened and the chamber was inspected after dispersion of aerosol. Suppression or burning of inflammable liquid was defined with help of decoded oscillogramme records or visually through the windows in the chamber cover.
The result was considered to be positive in case of suppression of all sources of fire within no longer than one minute after the end of burning of the FEAFM sample.
Method of FEAFM manufacturing is illustrated by the following examples, not limiting the scope of the present invention.
Example 1.
FEAFM has the following structure of components (mass parts):
Flame suppressing agent: potassium nitrate 58.0 potassium dipyrocatechol borate 10.0 Source of carbon: highly dispersed carbon 2.0 Stabilizer of chemical stability: centralite 0.3 diphenyl-amine 0.7 Technological Additives: diethylene glycol 1.0 lubricant (industrial) oil 1.0 sodium (zinc) stearate 0.1 Fuel-binder nitrocellulose 12.4 triacetine 9.0 polyvinyl acetate 2.0 Modifier of burning:
- catalyst: ferric oxide 1.5 - cooling agent: hydrated magnesium oxide 1.0 All loose components in specified proportions except potassium nitrate and stabilizer are entered in an apparatus of "Beken" type at environment temperature, mixed, and liquid components are added with dissolved centralite and diphenyl amine therein, mixed. At last, for the safety reasons, the apparatus is loaded with potassium nitrate and mixed not less than 30 mines. The obtained mixture is unloaded from the apparatus, is rolled and formed into elements of required sizes on a hydraulic or an auger-press at temperature 60-70'C.
Fire extinguishing efficiency of FEAFM according to the laboratory method of estimation comprises 10 g/m3 and in testing stand conditions according to the Standard UL 1058 - 25 g/m3.
Example 2.
F=.AFM has the following structure of components (mass parts):
rFlame suppressing agent: potassium nitrate 58.0 potassium ferrocyanide 10.0 Source of carbon: highly dispersed carbon . 2.0 Stabilizer: centralite 0.3 diphenyl-amine 0.7 Technological additives: diethylene glycol 1.0 lubricant (industrial) oil 1.0 sodium stearate 0.1 Fuel-binder nitrocellulose 11.9 triacetine 9.0 polyvinyl acetate 2.0 Modifier of burning: cobalt acetylacetonate , 2.0 magnesium hydroxide 1.0 This FEAFM was prepared similarly to example 1. Fire extinguishing efficiency the FIrAFM according to the laboratory method of estimation comprises 10 g/m3 and in testing stand conditions according to the Standard UL 1058 - 25 g/m3.
Example 3.
Preparation of the means was carried out according to the method of example 1.
Data on structure and efficiency i.s presented in the --table.
Example 4.
FEAFM has the following structure ~of components (mass parts):
rlame suppressing agent: potassium nitrate 50.0 potassium dipyrocatechol borate 5.0 Source of carbon: highly dispersed carbon 4.5 sorbitol 5.0 Stabilizer: centralite 0.5 Biphenyl-amine 0.5 Technological Additives: diethylene glycol 0.5 lubricant (industrial) oil 1.0 zinc stearate 0.07 sulforicinate 0.1 gelatin 0.03 ruel-binder nitrocellulose 13.8 mixture of diethylene glycol dinitrate with triethylene glycol dinitrate (7:3) 16.0 Modifier of burning: ferric oxide 2.0 hydrated magnesium oxide 1.0 Mixture of all components, except the flame suppressing agent and sorbitol, is performed in a mixer in a water environment at M 1:5 without additional heating of the equipment. To the mixer it is added nitrocellulose, technological additives (lubricant oil, diethylene glycol, zinc stearate) and. modifiers of burning. It is prepared separately emulsion of mixture of plasticizers with stabilizers of chemical stability (centralite and diphenyl-amine) with addition of emulsifier - sulforicinate and emulsion stabilizer - gelatin. The emulsion is added into the mixer and contents of the mixer is mixed for 18-24 hours. Then the received mixture is squeezed out of water on a squeezing apparatus up to humidity of 10-16 mass ~ and further in an apparatus without mechanical mixers is mixed with the flame suppressing agent and sorbitol during 20-30 minutes. The ready mix is rolled and is formed into elements of required size in a hydraulic or an auger-press at temperature 60-80°C.
Examples 5-6.
Preparation of the means was carried out according to the method of example 1.
Data on structure and efficiency is presented in the table.
Example 7.
Structure of FEAFM components, mass parts:
Flame suppressing agent: potassium nitrate 58.0 potassium dipyrocatechol 10.0 borate Source of carbon: carbon 2.0 Stabilizer: centralite 0.5 diphenyl-amine 0.5 Technological Additives: diethylene glycol 1.0 lubricant (industrial) oil 1.0 zinc stearate 0.1 Fuel-binder nitrocellulose 12.4 triacetine g.0 polyvinyl acetate 2.0 Modifier of burning:
- catalyst: ferric oxide 1.5 - cooling agent: heat-absorbing composition nitrocellulose 12.0 triacetine 9.8 polyvinyl acetate 2.0 basic magnesium ' carbonate 67.0 lubricant (industrial) oil 2.0 sodium stearate 0.2 oligoethyl dihydride siloxane 2.7 oleic acid 1.3 balance water 3.0 All components, except the cooling agent, are mixed in the "Beken" type apparatus similar to the used in example 1. The obtained mixture is rolled and is formed into elements or products also similar to 'example 1. Heat-absorbing composition is prepared separately. Mixing of all components in required proportions is carried out in the "Beken" type apparatus. Basic magnesium carbonate is initially processed by water emulsion of silicon-organic composition, oleic acid is added and mixed during 20-30 minutes, then, obtained emulsion is filtered up to humidity 50-70~. All liquid components are entered into mixing apparatus, mixed not less than 30 mines.
The obtained mixture is rolled at temperature 90-120°C
and formed on an auger-press into elements of required form and size. The obtained thus components of the means are mixed in the abovementioned ratio. Data on efficiency is specified in the table.
Example 8.
Preparation of the means was carried out according to the method of example 7.
Data on structure and efficiency is represented in the table.
The table Influence of structure of the proposed agent on efficiency thereof Structure of the means according to the present examples Contents of the Rus-t 2 3 4 5 6 7 8 components, sian mass parts Pa-tent No.
1 ~ 2 3 ~ 4 ~ 6 7 8 9 10 Flame 45-75 suppressing agent:
Potassium S8 58 53,9 50 54 64 59 40,5 nitrate Potassium 10 5 10 .10 5 dipyrocatechol borate potassium 10 ferrocyanide Potassium S
hexanitro cobaltate Source of 4-11 carbon:
Carbon ~ ~ 2 2 4 4,5 2 7,5 2 5 Sorbitol ~ 9 5 ~
Stabilizer: 0.5-2.0 Mixture of 1 1 1 1 0,5 1 1 1 centralite and diphenyl-amine Technological 0.52 additives: -3.0 Diethylene 1 2 0,1 0,5 1 0,5 1 1 glycol Lubricant oil ~ 1 1 1 1 1 1 1 1 Sodium (zinc) stearate 0.1 0.1 0.1 0.2 0.2 0.1 0.1 0,1 Fuel-binder 12-41, Nitrocellulose 12.4 11.9 12.4 13,8 12,4 12.4 12.4 12,4 Triacetine ~ 9 9 9 g g g g Plasticizer 16 LD-70*
Polyvinyl 2 2 2 2 2 2 2 acetate Modifier of 0.5-burning: 20 catalyst 1.5 2 1.5 2 2 1,5 1.5 3 inhibitor 20 cooling 1 1 1 1 5 1 100 5 agent Efficiency of the agent, 15- 10 20 10 8 20 12 40 35 g~m3 54 ~L1,-m - mixture of diethylene glycol nitrate with triethylene glycol dinitrate (7:3) It is clear from the presented tables, that in comparison with the known art, the lower level of fire extinguishing concentration is reduced, i.e. fire extinguishing efficiency is increased. In variants of FEAFM
embodiments, which have fire extinguishing efficiency at the level of the prior art, e.g., sample No. S, the fire extinguishing aerosol is characterized by lowered contents of toxic monoxide owing to the low contents of carbon therein. In embodiments according to samples 8 and 7 FEAFM
includes inhibitor and/or cooling agent in sufficient quantity and does not require to use additional cooling mans in case of using them in fire extinguishing devices.
Aerosol forming fire extinguishing composition according to the prior art is used in fire extinguishing devices together with a cooling agent with the purpose of obtaining a cooled flameless aerosol. Use of a cooling agent reduces efficiency (increases fire extinguishing concentration) due to settling of the aerosol in the layer of cooling agent. Fire extinguishing concentration in this case increases till 50-54 g/m3 and more.
Introduction into proposed FEAFM of~an inhibitor or a mixture thereof with a catalyst and/or a cooling agent in quantity more than 20 mass parts provides steady flameless gasification of FEAFM. Gasification character of FEAFM and large potential thereof for operational safety allows to use it as elements with highly developed surface, e.g., in the form of granules, that contributes to intensification of emitting of aerosol and faster filling the protected volume thereby, furthermore it is also economically favorable.
To eliminate getting through the flame in the FEAFM
granules layer it is reasonable to include a cooling agent in FEAFM in form of, e.g., metal shaving or minute elements of heat-absorbing composition, forming a mechanical mixture. The cooling agent in this case promotes formation of more loose structure of FEAFM, facilitating heat dissipation and simultaneously taking away additional amount of heat for self heating.
The cooling agent amount is determined by chemical composition, size of used FEAFM elements, feature of application thereof and a number of other factors.
In FEAFM without inhibitor the cooling agent contents can be high. Depending on the required purpose, e.g., on using oz FEAFM in devices intended for explosion and fire protection of objects, it is reasonable to use the generated tire extinguishing aerosol in cold condition, i.e. temperature thereof should be below than temperature of self-ignition of explosive mixtures, therefore quantity of the cooling agent in FEAFM can make up to 250 mass parts. The proposed FEAFM depending on structure and the quantities of the modifier of burning are characterized by wide spectrum of variability of characteristics thereof. By changing the ratio catalyst-inhibitor-cooling agent it is possible to adjust the process of thermal decomposition of FEAFM from flame burning till grading thereof into flameless gasification. As a rule, high-temperature aerosol has the most fine-disperse structure and is characterized by higher fire extinguishing efficiency and speed of aerosol generation. Flameless low-temperature aerosol has in some degree lesser tire extinguishing efficiency and lower speed of aerosol generation. Each of variants has, however, own advantages which could be realized in practice. High speed of aerosol generation promotes fast filling of protected volume and fast creation of fire extinguishing concentration therein, that allows to use fire extinguishing devices on basis of such FEAFM in untight, ventilated or extended objects, e.g., in vehicles engine compartments, cable channels etc. To protect tight volumes, in order to prevent sharp increase of pressure, it is reasonable to use fire extinguishing devices on the basis of FEAFM with lowered speed of aerosol generation.
The proposed invention considerably expands area of application of FEAFM due to the possibility of wide regulation of temperature of the generated fire extinguishing aerosol and speed of aerosol generation thereof, and can be used in various fire extinguishing devices, both with application of the cooling agent, and without it, which is a result of creation of FEAFM
embodiments with steady flameless gasification not requiring additional cooling of the aerosol.
The last circumstance considerably simplifies design of the apparatus, makes them less metal containing, simple in production, reliable in use. The aerosol generated by FEAFM, reliably extinguishes fires of various classes, provides retardation of dust-gas-air explosive mixtures.
Level of the basic characteristics of FEAFM
(physicochemical, mechanical, technological etc.) allows to manufacture elements of the various sizes and forms therefrom and to use them in fire extinguishing means.
The area of application of the proposed FEAFM in fire extinguishing devices is characterized by the widest spectrum: all kinds of automobile-, railroad, aviation-, water transport, underground railway, warehouses of inflammable liquids and fuels and lubricants, enterprises of various branches of industry, including objects with explosive dust-gas-air environment and extended communication network of power supply, ventilation, etc.
All devices using FEAFM can work in automatic and manual-operating modes, are designed for long service life (up to 10 years and longer), do not require additional service, are always ready to action. The means has low toxic level, is ozone safe, does not cause corrosion of metals, does not have destroying effect to material objects.
Thus FEAFM according to the present invention solves the stipulated problems completely.
As the catalyst, as a rule, there used compositions of metals of variable valence, e.g., oxides of iron, copper, nickel, cobalt, manganese, chrome; organic or inorganic compositions of same metals or mixtures thereof. The catalysts are added in FEAFM in quantity from 0.5 ~to 10 mass parts, preferably 1-5 mass parts.
Inhibitors of burning are added in FEAFM for reduction oz their speed of burning, decreasing of temperature of surface burning and flame zone. Damping of chemical reactions of burning is achieved either due to blocking the active centers of flame (gas) reactions by inhibitors or products of their decomposition, or due to intensification of reactions of carbonization, resulting in forming on the surface of burning of dense and hard carbon carcass changing conditions of mass- and heat exchange on the border of gaseous and condensed phases. Due to the reaction 2n CO = Cn + n COz contents of the toxic monoxide in gaseous products is decreased.
It is reasonable to use as the inhibitor of burning compositions chosen from classes: inorganic and organic phosphor- and/or nitrogen- containing composition, borates or carbonates of metals or hydroxides of metals of the III
group or mixtures thereof.
E.g., from phosphor- and nitrogen- containing inhibitors it is preferable to use phosphates of potassium, calcium, iron of any degree of displacement; triphenyl phosphate; ammonium phosphates, ferric-ammonium phosphate, ammonium oxalate, ferric-ammonium oxalate; amides-carbamide, triazine and its derivatives, dicyanamide; among borates of metals - borates of potassium, sodium, calcium, magnesium, barium, zinc.
Quantity of entered inhibitor comprises 5-30 mass parts, preferably 15-25 mass parts.
The cooling agents are added in FEAFM for change of its thermal balance of burning. Additional reduction of temperature on the surface, and cooling of products of burning of FEAFM occurs due to physical removing of heat which is spent on heating of particles of the entered cooling agent, its endothermic decomposition, and also due to shielding of the thermal flow directed from the zone of flame reactions to the burning surface.
As the cooling agent there are used oxides and hydroxides of metals of the II group, aluminosilicates, nepheline, metal shavings or mixtures thereof, or a heat-absorbing composition.
Incombustible products of disintegration of the composition dilute products of FEAFM burning in the flame zone of reaction, reduce temperature of the flame and with it decrease return thermal flow to the surface of burning.
Interaction of FEAFM combustion products with products of disintegration of the heat-absorbing composition results in "freezing" thereof, possibility of their further interaction is eliminated, in result, it is generated a cooled aerosol. Heat-absorbing composition includes the following ingredients, mass parts:
heat-absorbing component 50-80 binder 10-35, additives 1-7, thus, as the heat-absorbing component there are mainly used carbonates or basic carbonates, phosphates of metals of the II group; crystal hydrides thereof, hydroxides of metals of the III group or mixtures thereof; as the binder -derivatives of cellulose, e.g., nitrocellulose, plasticized by a low-volatile plasticizes , e.g., triacetin and/or dibutil phthalate, and polyvinyl acetate or polyvinyl a alcohol; as the additive it is used lubricant oil, potassium or zinc stearate, organosilicon compositions and oleic acid.
Depending on the purpose and application of FEAFM in a particular fire extinguishing device, quantity of the cooling agent can vary over a wide range from 0.5 to 250 mass harts.
Lubricant oil, composition chosen from the class of glycoles, or glycerin, salt of a fatty acid, e.g., potassium or zinc stearate or mixture thereof with sulforicinate and gelatin are used in F1;AFM as the technological additives.
Introduction in F>;AFM of compositions from the class of glycoles such as diethylene glycol, triethylene glycol, or glycerin is caused by their lubricating action. Therefore they are used in quantities from 0.1 to 2 mass parts as additional technological additives lowering external friction and the phenomenon of sticking to the technological equipment during manufacturing of FEAFM and processing thereof in various products (aerosol forming elements). The best efficiency is shown with the technological additive including a triple mixture of:
lubricant oil, diethylene glycol (triethylene glycol or glycerin) and a salt of a fatty acid.
Diethylene glycol or triethylene glycol serves simultaneously as a plasticizes for cellulose derivatives, in particular, for nitrocellulose, and as an additive in _ small quantities (2-5 mass parts) to the base plasticizer it improves process of plasticization of nitrocellulose.
Manufacturing of FEAFM is carried out by mixing of all components in required proportions in an apparatus having an agitator using a dry method or in water environment (for water insoluble nitrate plasticizers) at temperature 10-55°C with subsequent forming from the received mixture of elements of necessary sizes and configuration at temperature 50-80°C. In case of in-water manufacturing of FEAFM the fire extinguishing agent is added to the mixture pressed out of water. In case of using as the cooling agent of heat-absorbing composition manufacturing thereof and forming of dements is carried out by the same way; in this case F~ArM is produced without cooling agent, and then it is performed mixing thereof or elements are used in layers.
The main characteristic of FEAFM is its fire extinguishing efficiency (FEE), i.e. minimal weight of rFEAFM, ensuring suppression of the fire in 1 m3 of protected volume.
FEE of FEAFM compositions was extensively examined in laboratory and testing stand conditions at suppression of inflammable liquids (acetone, petrol, ethyl and isopropyl alcohols, mixture of diesel fuel wit.h~ petrol) and was confirmed by tests of aerosol generators on their basis.
Laboratory technique of FEE estimation consist in following. In an exhaust hood under a glass cap of 10 1 capacity there was placed a burning alcohol-lamp or a melting-pot with inflammable liquid and a certain weight Sample Of FEAFM, connected with a Nichrome spiral. Using electric current with about 12 V voltage supplied to the Nichrome spiral it was set fire the sample of FEAFM and the process of suppression of the flame of the alcohol-limp (or inflammable liquid) was observed through the transparent glass of the cap. The result was considered to be positive if the flame was suppressed during period no longer than 5 s after burning away the sample of FEAFM. Minimal fire extinguishing concentration was determined by interpolation on two nearest points. For comparison it was carried out a check experiment on burning an alcohol-lamp (or inflammable liquid in a melting-pot) under the closed cap. Time of natural dying of the alcohol-lamp flame, due to consumption of oxygen of air enclosed under the cap, was 75 s.
American Standard UL 1058 was laid in base of testing stand technique of examination of FEAFM fire extinguishing efficiency.
In a chamber of 1 m3 volume (2.08 x 0.8 x 0.6) , having a flat screen of 0.25 m width in the middle part on whole height of the chamber, there were placed 5 sources of inflammable liauid (capacities of 75 mm in diameter, 125 mm in height with 500 ml of petrol in each of them), which were placed on four corners of the chamber and one source was placed behind the screen. Above each source of inflammable liquid in the cover of chamber there were formed small windows made of organic glass for visual observation for suppression of the fire.
The tested sample of FEAFM was placed in a metal housing and was fixed in the central part of the side wall of the chamber. Initiation of ignition of the FEAFM sample was performed using a fuse or a source of electric current located outside of the testing chamber. Petrol or another inflammable liquid in capacities was ignited, the cover of testing chamber was closed. After steady burning of inflammable liquid during 30 s it was initiated ignition of the FEAFM sample. And after 1 more minute the cover of chamber was opened and the chamber was inspected after dispersion of aerosol. Suppression or burning of inflammable liquid was defined with help of decoded oscillogramme records or visually through the windows in the chamber cover.
The result was considered to be positive in case of suppression of all sources of fire within no longer than one minute after the end of burning of the FEAFM sample.
Method of FEAFM manufacturing is illustrated by the following examples, not limiting the scope of the present invention.
Example 1.
FEAFM has the following structure of components (mass parts):
Flame suppressing agent: potassium nitrate 58.0 potassium dipyrocatechol borate 10.0 Source of carbon: highly dispersed carbon 2.0 Stabilizer of chemical stability: centralite 0.3 diphenyl-amine 0.7 Technological Additives: diethylene glycol 1.0 lubricant (industrial) oil 1.0 sodium (zinc) stearate 0.1 Fuel-binder nitrocellulose 12.4 triacetine 9.0 polyvinyl acetate 2.0 Modifier of burning:
- catalyst: ferric oxide 1.5 - cooling agent: hydrated magnesium oxide 1.0 All loose components in specified proportions except potassium nitrate and stabilizer are entered in an apparatus of "Beken" type at environment temperature, mixed, and liquid components are added with dissolved centralite and diphenyl amine therein, mixed. At last, for the safety reasons, the apparatus is loaded with potassium nitrate and mixed not less than 30 mines. The obtained mixture is unloaded from the apparatus, is rolled and formed into elements of required sizes on a hydraulic or an auger-press at temperature 60-70'C.
Fire extinguishing efficiency of FEAFM according to the laboratory method of estimation comprises 10 g/m3 and in testing stand conditions according to the Standard UL 1058 - 25 g/m3.
Example 2.
F=.AFM has the following structure of components (mass parts):
rFlame suppressing agent: potassium nitrate 58.0 potassium ferrocyanide 10.0 Source of carbon: highly dispersed carbon . 2.0 Stabilizer: centralite 0.3 diphenyl-amine 0.7 Technological additives: diethylene glycol 1.0 lubricant (industrial) oil 1.0 sodium stearate 0.1 Fuel-binder nitrocellulose 11.9 triacetine 9.0 polyvinyl acetate 2.0 Modifier of burning: cobalt acetylacetonate , 2.0 magnesium hydroxide 1.0 This FEAFM was prepared similarly to example 1. Fire extinguishing efficiency the FIrAFM according to the laboratory method of estimation comprises 10 g/m3 and in testing stand conditions according to the Standard UL 1058 - 25 g/m3.
Example 3.
Preparation of the means was carried out according to the method of example 1.
Data on structure and efficiency i.s presented in the --table.
Example 4.
FEAFM has the following structure ~of components (mass parts):
rlame suppressing agent: potassium nitrate 50.0 potassium dipyrocatechol borate 5.0 Source of carbon: highly dispersed carbon 4.5 sorbitol 5.0 Stabilizer: centralite 0.5 Biphenyl-amine 0.5 Technological Additives: diethylene glycol 0.5 lubricant (industrial) oil 1.0 zinc stearate 0.07 sulforicinate 0.1 gelatin 0.03 ruel-binder nitrocellulose 13.8 mixture of diethylene glycol dinitrate with triethylene glycol dinitrate (7:3) 16.0 Modifier of burning: ferric oxide 2.0 hydrated magnesium oxide 1.0 Mixture of all components, except the flame suppressing agent and sorbitol, is performed in a mixer in a water environment at M 1:5 without additional heating of the equipment. To the mixer it is added nitrocellulose, technological additives (lubricant oil, diethylene glycol, zinc stearate) and. modifiers of burning. It is prepared separately emulsion of mixture of plasticizers with stabilizers of chemical stability (centralite and diphenyl-amine) with addition of emulsifier - sulforicinate and emulsion stabilizer - gelatin. The emulsion is added into the mixer and contents of the mixer is mixed for 18-24 hours. Then the received mixture is squeezed out of water on a squeezing apparatus up to humidity of 10-16 mass ~ and further in an apparatus without mechanical mixers is mixed with the flame suppressing agent and sorbitol during 20-30 minutes. The ready mix is rolled and is formed into elements of required size in a hydraulic or an auger-press at temperature 60-80°C.
Examples 5-6.
Preparation of the means was carried out according to the method of example 1.
Data on structure and efficiency is presented in the table.
Example 7.
Structure of FEAFM components, mass parts:
Flame suppressing agent: potassium nitrate 58.0 potassium dipyrocatechol 10.0 borate Source of carbon: carbon 2.0 Stabilizer: centralite 0.5 diphenyl-amine 0.5 Technological Additives: diethylene glycol 1.0 lubricant (industrial) oil 1.0 zinc stearate 0.1 Fuel-binder nitrocellulose 12.4 triacetine g.0 polyvinyl acetate 2.0 Modifier of burning:
- catalyst: ferric oxide 1.5 - cooling agent: heat-absorbing composition nitrocellulose 12.0 triacetine 9.8 polyvinyl acetate 2.0 basic magnesium ' carbonate 67.0 lubricant (industrial) oil 2.0 sodium stearate 0.2 oligoethyl dihydride siloxane 2.7 oleic acid 1.3 balance water 3.0 All components, except the cooling agent, are mixed in the "Beken" type apparatus similar to the used in example 1. The obtained mixture is rolled and is formed into elements or products also similar to 'example 1. Heat-absorbing composition is prepared separately. Mixing of all components in required proportions is carried out in the "Beken" type apparatus. Basic magnesium carbonate is initially processed by water emulsion of silicon-organic composition, oleic acid is added and mixed during 20-30 minutes, then, obtained emulsion is filtered up to humidity 50-70~. All liquid components are entered into mixing apparatus, mixed not less than 30 mines.
The obtained mixture is rolled at temperature 90-120°C
and formed on an auger-press into elements of required form and size. The obtained thus components of the means are mixed in the abovementioned ratio. Data on efficiency is specified in the table.
Example 8.
Preparation of the means was carried out according to the method of example 7.
Data on structure and efficiency is represented in the table.
The table Influence of structure of the proposed agent on efficiency thereof Structure of the means according to the present examples Contents of the Rus-t 2 3 4 5 6 7 8 components, sian mass parts Pa-tent No.
1 ~ 2 3 ~ 4 ~ 6 7 8 9 10 Flame 45-75 suppressing agent:
Potassium S8 58 53,9 50 54 64 59 40,5 nitrate Potassium 10 5 10 .10 5 dipyrocatechol borate potassium 10 ferrocyanide Potassium S
hexanitro cobaltate Source of 4-11 carbon:
Carbon ~ ~ 2 2 4 4,5 2 7,5 2 5 Sorbitol ~ 9 5 ~
Stabilizer: 0.5-2.0 Mixture of 1 1 1 1 0,5 1 1 1 centralite and diphenyl-amine Technological 0.52 additives: -3.0 Diethylene 1 2 0,1 0,5 1 0,5 1 1 glycol Lubricant oil ~ 1 1 1 1 1 1 1 1 Sodium (zinc) stearate 0.1 0.1 0.1 0.2 0.2 0.1 0.1 0,1 Fuel-binder 12-41, Nitrocellulose 12.4 11.9 12.4 13,8 12,4 12.4 12.4 12,4 Triacetine ~ 9 9 9 g g g g Plasticizer 16 LD-70*
Polyvinyl 2 2 2 2 2 2 2 acetate Modifier of 0.5-burning: 20 catalyst 1.5 2 1.5 2 2 1,5 1.5 3 inhibitor 20 cooling 1 1 1 1 5 1 100 5 agent Efficiency of the agent, 15- 10 20 10 8 20 12 40 35 g~m3 54 ~L1,-m - mixture of diethylene glycol nitrate with triethylene glycol dinitrate (7:3) It is clear from the presented tables, that in comparison with the known art, the lower level of fire extinguishing concentration is reduced, i.e. fire extinguishing efficiency is increased. In variants of FEAFM
embodiments, which have fire extinguishing efficiency at the level of the prior art, e.g., sample No. S, the fire extinguishing aerosol is characterized by lowered contents of toxic monoxide owing to the low contents of carbon therein. In embodiments according to samples 8 and 7 FEAFM
includes inhibitor and/or cooling agent in sufficient quantity and does not require to use additional cooling mans in case of using them in fire extinguishing devices.
Aerosol forming fire extinguishing composition according to the prior art is used in fire extinguishing devices together with a cooling agent with the purpose of obtaining a cooled flameless aerosol. Use of a cooling agent reduces efficiency (increases fire extinguishing concentration) due to settling of the aerosol in the layer of cooling agent. Fire extinguishing concentration in this case increases till 50-54 g/m3 and more.
Introduction into proposed FEAFM of~an inhibitor or a mixture thereof with a catalyst and/or a cooling agent in quantity more than 20 mass parts provides steady flameless gasification of FEAFM. Gasification character of FEAFM and large potential thereof for operational safety allows to use it as elements with highly developed surface, e.g., in the form of granules, that contributes to intensification of emitting of aerosol and faster filling the protected volume thereby, furthermore it is also economically favorable.
To eliminate getting through the flame in the FEAFM
granules layer it is reasonable to include a cooling agent in FEAFM in form of, e.g., metal shaving or minute elements of heat-absorbing composition, forming a mechanical mixture. The cooling agent in this case promotes formation of more loose structure of FEAFM, facilitating heat dissipation and simultaneously taking away additional amount of heat for self heating.
The cooling agent amount is determined by chemical composition, size of used FEAFM elements, feature of application thereof and a number of other factors.
In FEAFM without inhibitor the cooling agent contents can be high. Depending on the required purpose, e.g., on using oz FEAFM in devices intended for explosion and fire protection of objects, it is reasonable to use the generated tire extinguishing aerosol in cold condition, i.e. temperature thereof should be below than temperature of self-ignition of explosive mixtures, therefore quantity of the cooling agent in FEAFM can make up to 250 mass parts. The proposed FEAFM depending on structure and the quantities of the modifier of burning are characterized by wide spectrum of variability of characteristics thereof. By changing the ratio catalyst-inhibitor-cooling agent it is possible to adjust the process of thermal decomposition of FEAFM from flame burning till grading thereof into flameless gasification. As a rule, high-temperature aerosol has the most fine-disperse structure and is characterized by higher fire extinguishing efficiency and speed of aerosol generation. Flameless low-temperature aerosol has in some degree lesser tire extinguishing efficiency and lower speed of aerosol generation. Each of variants has, however, own advantages which could be realized in practice. High speed of aerosol generation promotes fast filling of protected volume and fast creation of fire extinguishing concentration therein, that allows to use fire extinguishing devices on basis of such FEAFM in untight, ventilated or extended objects, e.g., in vehicles engine compartments, cable channels etc. To protect tight volumes, in order to prevent sharp increase of pressure, it is reasonable to use fire extinguishing devices on the basis of FEAFM with lowered speed of aerosol generation.
The proposed invention considerably expands area of application of FEAFM due to the possibility of wide regulation of temperature of the generated fire extinguishing aerosol and speed of aerosol generation thereof, and can be used in various fire extinguishing devices, both with application of the cooling agent, and without it, which is a result of creation of FEAFM
embodiments with steady flameless gasification not requiring additional cooling of the aerosol.
The last circumstance considerably simplifies design of the apparatus, makes them less metal containing, simple in production, reliable in use. The aerosol generated by FEAFM, reliably extinguishes fires of various classes, provides retardation of dust-gas-air explosive mixtures.
Level of the basic characteristics of FEAFM
(physicochemical, mechanical, technological etc.) allows to manufacture elements of the various sizes and forms therefrom and to use them in fire extinguishing means.
The area of application of the proposed FEAFM in fire extinguishing devices is characterized by the widest spectrum: all kinds of automobile-, railroad, aviation-, water transport, underground railway, warehouses of inflammable liquids and fuels and lubricants, enterprises of various branches of industry, including objects with explosive dust-gas-air environment and extended communication network of power supply, ventilation, etc.
All devices using FEAFM can work in automatic and manual-operating modes, are designed for long service life (up to 10 years and longer), do not require additional service, are always ready to action. The means has low toxic level, is ozone safe, does not cause corrosion of metals, does not have destroying effect to material objects.
Thus FEAFM according to the present invention solves the stipulated problems completely.
Claims (10)
1, The fire extinguishing aerosol forming means including a frame suppressing agent, a fuel-binder, a source of carbon, a stabilizer, a modifier of burning and technological additives, characterized in that, said means contains nitrates of alkaline metals or mixture thereof with complex compositions of alkaline metals as the flame suppressing agent, carbon as such, aliphatic or aromatic alcohols, or mixture thereof as the source of carbon, it additionally contains a cooling agent oxides and hydroxides of metals of the II group, aluminosilicates, nepheline or metal shaving or mixture thereof as the modifier of burning, or a heat absorbing composition, and it additionally contains compositions chosen from the class of glycoles or glycerin as the technological additives.
2. The means according to claim 1, characterized in that, it contains ingredients in the following ratio, mass parts:
flame suppressing agent ~40 - 80;
fuel-binder~~~12 - 40;
source of carbon~~1 - 15;
stabilizer~~~0.5 - 2.5;
modifier of burning~~1 - 250;
technological additives~~0.5 - 7.5.
flame suppressing agent ~40 - 80;
fuel-binder~~~12 - 40;
source of carbon~~1 - 15;
stabilizer~~~0.5 - 2.5;
modifier of burning~~1 - 250;
technological additives~~0.5 - 7.5.
3. The means according to claim 1, characterized in that, it contains a lubricant oil, a salt of a greasy acid, e.g., sodium or zinc stearate, or a mixture of the salt with sulforicinate and gelatin as the technological additives.
4. The means according to claim 1, characterized in that, it contains a catalyst and/or an inhibitor as the modifier of burning and the cooling agent.
5. The means according to claim 4, characterized in that, the heat absorbing composition includes a heat-absorbing component, a binder and additives in the following ratio, mass parts:
heat-absorbing component~~50 - 80;
binder~~~~~10 - 35;
additives~~~~1 - 7.
heat-absorbing component~~50 - 80;
binder~~~~~10 - 35;
additives~~~~1 - 7.
6. The means according to claim 5, characterized in that, it contains a derivative of cellulose, a low-volatile plasticizer and polyvinyl acetate or polyvinyl alcohol as the binder in the following ratio of the ingredients, mass parts:
derivative of cellulose and low-volatile plasticizer~~~9 - 34;
polyvinyl acetate or polyvinyl alcohol~~1 - 5.
derivative of cellulose and low-volatile plasticizer~~~9 - 34;
polyvinyl acetate or polyvinyl alcohol~~1 - 5.
7. The means according to claim 5, characterized in that, it contains carbonates, basic carbonates or phosphates of metals of the II group, crystal hydrides thereof or hydroxides of metals of the III group or mixtures thereof as the heat absorbing component.
8. The means according to claim 5, characterized in that, it contains a lubricant oil, a sodium or zinc stearate, organosilicon compositions, an oleic acid as the additives.
9. The means according to claim 4, characterized in that, it contains a composition chosen from the sequence including oxides of metals of variable valence, their organic or inorganic compositions, or mixture thereof as the catalyst.
10. The means according to claim 4, characterized in that, it contains a composition chosen from the sequence including inorganic and organic phosphorus-and/or nitrogen- containing compositions, hydroxides of metals of the III
group, borates or carbonates of metals or mixture thereof as an inhibitor.
group, borates or carbonates of metals or mixture thereof as an inhibitor.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| RU98117411/12A RU2146546C1 (en) | 1998-09-11 | 1998-09-11 | Fire-extinguishing aerosol-generating agent |
| RU98117411 | 1998-09-11 | ||
| PCT/RU1999/000269 WO2000015305A1 (en) | 1998-09-11 | 1999-08-03 | Fire extinguishing aerosol forming means |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2348644A1 true CA2348644A1 (en) | 2000-03-23 |
Family
ID=20210583
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002348644A Abandoned CA2348644A1 (en) | 1998-09-11 | 1999-08-03 | Fire extinguishing aerosol forming means |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP1109601B1 (en) |
| CN (1) | CN1150046C (en) |
| AT (1) | ATE231018T1 (en) |
| AU (1) | AU754475B2 (en) |
| BR (1) | BR9913567A (en) |
| CA (1) | CA2348644A1 (en) |
| DE (1) | DE69904950T2 (en) |
| MY (1) | MY133539A (en) |
| RU (1) | RU2146546C1 (en) |
| WO (1) | WO2000015305A1 (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7337856B2 (en) | 2003-12-02 | 2008-03-04 | Alliant Techsystems Inc. | Method and apparatus for suppression of fires |
| US20050115721A1 (en) | 2003-12-02 | 2005-06-02 | Blau Reed J. | Man-rated fire suppression system |
| WO2010137933A1 (en) * | 2009-05-26 | 2010-12-02 | Boris Jankovski | Gas generating charges for aerosol fire suppression devices and their production technology |
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| CN101757760B (en) * | 2010-01-19 | 2012-06-27 | 陕西坚瑞消防股份有限公司 | Catalytic chemical coolant for hot aerosol and preparation method thereof |
| US8939225B2 (en) | 2010-10-07 | 2015-01-27 | Alliant Techsystems Inc. | Inflator-based fire suppression |
| CN102949802B (en) * | 2011-08-16 | 2016-04-06 | 西安坚瑞安全应急设备有限责任公司 | A kind of fire-extinguishing composite containing organic acid compound |
| CN102949804A (en) * | 2011-08-25 | 2013-03-06 | 丁一 | Pollution-free gaseous extinguishant |
| US8967284B2 (en) | 2011-10-06 | 2015-03-03 | Alliant Techsystems Inc. | Liquid-augmented, generated-gas fire suppression systems and related methods |
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| CN103170084B (en) * | 2011-12-20 | 2016-04-06 | 西安坚瑞安全应急设备有限责任公司 | A kind of metal-carbonyl fire-extinguishing composite |
| CN102772877A (en) * | 2012-07-10 | 2012-11-14 | 启东市中勇机电工具有限公司 | Fire extinguishing agent |
| CN102824715A (en) | 2012-09-21 | 2012-12-19 | 陕西坚瑞消防股份有限公司 | Phosphate fire extinguishing composition |
| CN103990246B (en) * | 2014-04-25 | 2017-04-19 | 深圳市鸿海盛特种消防科技有限公司 | Extinguishing agent, engine compartment extinguishing apparatus using it, and engine compartment extinguishing method |
| CN108785911B (en) * | 2018-06-22 | 2019-08-09 | 国网湖南省电力有限公司 | A kind of transformer oil extinguishing chemical and fire extinguishing system |
| CN113939346B (en) * | 2019-06-19 | 2023-10-27 | 塞拉诺瓦有限公司 | Aerosol-forming composition for fire extinguishing |
| CN112675462A (en) * | 2020-01-20 | 2021-04-20 | 湖北及安盾消防科技有限公司 | Pulse type fire extinguishing device and electrical equipment |
| CN112521916A (en) * | 2020-12-14 | 2021-03-19 | 北京星日消防技术有限公司 | Chemical compound type coolant for aerosol fire extinguishing product and preparation method thereof |
| CN114129948A (en) * | 2021-11-16 | 2022-03-04 | 湖北及安盾消防科技有限公司 | Aerosol composition, method for producing the same, and fire extinguishing agent |
| CN116159276A (en) * | 2023-02-27 | 2023-05-26 | 湖北及安盾消防科技有限公司 | Self-cooling flameless hot aerosol fire extinguishing agent and preparation method thereof |
| CN116328246B (en) * | 2023-03-16 | 2024-03-12 | 湖北及安盾消防科技有限公司 | Combined type hot aerosol fire extinguishing agent and preparation method thereof |
| CN116492632A (en) * | 2023-05-11 | 2023-07-28 | 北京菲思拓新材料股份有限公司 | Aerosol fire extinguishing agent |
| CN116943090A (en) * | 2023-06-13 | 2023-10-27 | 湖北及安盾消防科技有限公司 | Chemical coolant and application thereof in K-type aerosol fire extinguishing agent |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2006239C1 (en) * | 1992-02-21 | 1994-01-30 | Люберецкое научно-производственное объединение "Союз" | Aerosol-forming fire-extinguishing composition |
| DE69206399T2 (en) * | 1992-03-19 | 1996-07-04 | Spectronix Ltd | Fire extinguishing process. |
| RU2105581C1 (en) * | 1995-04-07 | 1998-02-27 | Зиновий Петрович Пак | Composition for fire extinguishing |
| RU2086278C1 (en) * | 1995-06-26 | 1997-08-10 | Люберецкое научно-производственное объединение "Союз" | Composition for cooling fire-extinguishing aerosol and method of manufacture thereof |
| DE19531130A1 (en) * | 1995-08-24 | 1997-02-27 | Bayern Chemie Gmbh Flugchemie | Granulated or pelleted gas generating substance, suitable for use in airbags |
| RU2091106C1 (en) * | 1996-04-26 | 1997-09-27 | Федеральный центр двойных технологий "Союз" | Aerosol forming fire-extinguishing compound |
-
1998
- 1998-09-11 RU RU98117411/12A patent/RU2146546C1/en not_active IP Right Cessation
-
1999
- 1999-08-03 EP EP99938680A patent/EP1109601B1/en not_active Expired - Lifetime
- 1999-08-03 AT AT99938680T patent/ATE231018T1/en not_active IP Right Cessation
- 1999-08-03 CA CA002348644A patent/CA2348644A1/en not_active Abandoned
- 1999-08-03 BR BR9913567-1A patent/BR9913567A/en not_active IP Right Cessation
- 1999-08-03 WO PCT/RU1999/000269 patent/WO2000015305A1/en active IP Right Grant
- 1999-08-03 AU AU53110/99A patent/AU754475B2/en not_active Ceased
- 1999-08-03 CN CNB998119849A patent/CN1150046C/en not_active Expired - Fee Related
- 1999-08-03 DE DE69904950T patent/DE69904950T2/en not_active Expired - Lifetime
- 1999-08-11 MY MYPI99003441A patent/MY133539A/en unknown
Also Published As
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| EP1109601B1 (en) | 2003-01-15 |
| DE69904950D1 (en) | 2003-02-20 |
| AU754475B2 (en) | 2002-11-14 |
| MY133539A (en) | 2007-11-30 |
| CN1323236A (en) | 2001-11-21 |
| BR9913567A (en) | 2001-05-22 |
| EP1109601A1 (en) | 2001-06-27 |
| AU5311099A (en) | 2000-04-03 |
| WO2000015305A1 (en) | 2000-03-23 |
| DE69904950T2 (en) | 2003-11-06 |
| CN1150046C (en) | 2004-05-19 |
| RU2146546C1 (en) | 2000-03-20 |
| ATE231018T1 (en) | 2003-02-15 |
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