Fire extinguishing composition comprising alcohol phenol compound and derivative thereof

Information

  • Patent Grant
  • 10035033
  • Patent Number
    10,035,033
  • Date Filed
    Wednesday, March 11, 2015
    9 years ago
  • Date Issued
    Tuesday, July 31, 2018
    6 years ago
Abstract
The present invention relates to a fire-extinguishing composition containing an alcohol/phenol compound and its derivative. The fire-extinguishing composition releases a great quantity of active fire-extinguishing particles by making use of the heat generated from combustion of a pyrotechnic agent. The fire-extinguishing composition containing an alcohol/phenol compound and its derivative in the present invention reacts at a high temperature to generate a great quantity of nanoscale active fire-extinguishing particles, takes reaction with one or more of O-, OH-, H-free radicals necessary for a chain combustion reaction, so as to cut off the chain combustion reaction and take physical and chemical inhibiting effects to jointly achieve a fire extinguishing effect at the same time. Meanwhile, it takes a synergistic interaction effect with pyrotechnic agent to further raise the fire extinguishing efficiency of the fire extinguishing agent and greatly shorten the effective fire extinguishing time.
Description
RELATED APPLICATIONS

This application is the U.S. National Stage of International Application No. PCT/CN2015/074045, filed Mar. 11, 2015, which designates the U.S., published in Chinese, and claims priority under 35 U.S.C. §§ 119 or 365(c) to China (PRC) Application No. CN 201410014330.6, filed Jan. 13, 2014. The entire teachings of the above applications are incorporated herein by reference.


FIELD OF THE INVENTION

The present invention pertains to the technical field of aerosol fire distinguishing, particularly to a thermal aerosol fire-extinguishing composition.


BACKGROUND OF THE INVENTION

Since the specific target of each country for substitution of Halon fire extinguishing agents was put forth in Canadian Montreal Convention in 1987, all countries in the world have been committed to the research of new fire extinguishing techniques. Fire extinguishing techniques with high fire extinguishing efficiency and no environmental pollution are aims of our effort.


A gas fire extinguishing system, a powder extinguishing system and, a water fire extinguishing system and the like are harmless to environment, so they are selected as substitutes of Halon fire extinguishing agents and are widely used. The fire extinguishing mechanism of the fire extinguishing systems of carbon dioxide, IG541 and inert gases mainly relies on physical fire extinguishing. The fire is put out by lowering the concentration of oxygen in the firing area. This fire extinguishing method would easily threaten human safety. The powder extinguishing system puts out a fire by spraying powder under the action of pressurized gas to contact flame and realize physical and chemical suppression effect. A water mist fire extinguishing system achieves the objects of controlling, suppressing and putting out a fire through triple actions of cooling, smothering, and isolation of thermal radiation by using water mist.


However, all these fire extinguishing systems need high pressure storage. Not only the volume is large but also there is a risk of physical explosion during storage. A document “Safety Analysis of Gas Fire Extinguishing System” (Fire Science and Technology 2002 21(5)) analyzes the risk of a gas fire extinguishing system and enumerates the safety accidents triggered by the stored pressure gas fire extinguishing system during use.


The existing thermal aerosol fire extinguishing agents are mainly type S and type K fire extinguishing agents. The comprehensive analysis of their performance and features indicates that their fire extinguishing mechanism is that the thermal aerosol fire extinguishing agents take a redox reaction through agent combustion to release a great quantity of gas and active particles and the goal of integrated chemical and physical fire extinguishing is realized through the chain scission reaction of the active particles and covering and smothering of a great quantity of gas. The disadvantage of the thermal aerosol fire extinguishing agents is that the thermal aerosol fire extinguishing agent will release a great quantity of heat while it takes the combustion reaction to release the thermal aerosol, which may cause a secondary combustion. In order to effectively reduce the temperature of the device and aerosol and avoid the secondary fire, a cooling system needs to be added. The cooling materials of the existing thermal aerosol fire extinguishing units can reduce the temperature of products, but they also greatly weaken the fire extinguishing performance of the products. In order to make up the loss on the fire extinguishing performance caused by the cooling system, many products either lower the fire extinguishing level or continuously increase the mass of the actual fire extinguishing agent, rendering the increase of product volume and the decrease of use efficiency, which results in a complex and cumbersome structure of the device, a complex technological process, a high cost, and a high nozzle temperature, which would easily cause injury to fire fighters.


SUMMARY OF THE INVENTION

Regarding the current situation of existing fire extinguishing devices, particularly the inherent defects of an aerosol fire extinguishing system, an object of the present invention is to provide a safer and more efficient fire-extinguishing composition.


The technical scheme of the present invention is:


A fire-extinguishing composition containing an alcohol/phenol compound and its derivative, wherein the fire-extinguishing composition contains an alcohol/phenol compound and its derivative; the fire-extinguishing composition releases a great quantity of active fire-extinguishing particles by making use of combustion of a pyrotechnic agent.


Further, the mass content of the alcohol/phenol compound in the fire-extinguishing composition is 30% or above.


Further, the alcohol/phenol compound and its derivative comprise one or more of a monohydric alcohol/phenol compound and its derivative, a dihydric alcohol/phenol compound and its derivative, and a polyhydric alcohol/phenol compound and its derivative.


Further, the monohydric alcohol/phenol compound and its derivative comprise: 3-aminobenzyl alcohol, 2,3,5-trimethylphenol, magnesium ethoxide, benzilic acid, benzhydrol, 4-hydroxy-3-methoxybenzyl alcohol, octadecanol, 2-(4-hydroxyphenyl) ethanol, 2-nitrobenzyl alcohol, 2-(β-ethoxy) amino-5-nitro, phenoxyethanol, 2,2-dimethyl-1-propanol, 1-adamantanol, lithium tert-butoxide, cholesterol, 2,6,7-trioxa-1-phosphabicyclo (2,2,2) octane-4-methanol-1 (pentaerythritol octahydrogen tetraphosphate), 3-(3,5-di-tert-butyl-4-hydroxyphenyl) propanoic acid octadecyl ester, 5-indanol, β-sitosterol, piroctone olamine, 4-methylbenzyl alcohol, sodium methoxide, sodium trimethylsilanolate, triphenylcarbinol, potassium tert-butoxide, sodium tert-butoxide, tetramethyl piperidinol, tebuconazole, ethanolamine hydrochloride, potassium ethoxide, sodium glycollate, 2.3-dimethylphenol, 2.5-dimethylphenol, 2-amino-5-chlorophenol, 2-amino-5-nitrophenol, 2,6-dichlorophenol, 2-aminophenol, 2,4,6-trimethylphenol, 2,4,6-tribromophenol, 2,4-di-tert-butyl-6-(5-chloro-2H-benzotriazole-2-yl) phenol, 2,4-di-tert-butylphenol, 2,4-di-tert-butylphenol, 2 phenylphenol, 2,5-dichlorothiophenol, 2,6-di-tert-butyl-p-cresol, 2,6-tert-butyl-4-cresol, 2-methyl-3-nitrophenol, 2-methyl-5-aminophenol, 2-chloro-4-fluorophenol, 2-chloro-4-methoxyphenol, 2-chloro-4-bromophenol, 2-naphthol, 2-naphthol, 2-hydroxypyridine, 2-tert-butyl-5-cresol, 2-bromo-4-cresol, 2-bromo-p-cresol, 1-amino-7-naphthol, 1-naphthol, 1-bromo-2-naphthol, 2-(2H-benzotriazole-2-yl)-4,6-di-tert-pentylphenol, 2-(5-bromo-2-pyridine) azo-5-(diethylamino)phenol, 2,2′-diphenol, 2,2′-binaphthol, 2,2-methylenebis [6-benzotriazole-2-yl]-4-tert-octylphenol, 2,3,5-trimethylphenol, 2,3,6-trimethylphenol, 2,3-dichlorophenol, 2-nitroso-1-naphthol, 2-ethoxy-5-(1-propenyl) phenol, 2-ethoxyphenol, 2-isopropylephenol, 3,4-xylenol, 3,4-dimethylphenol, 3,4-dimethoxyphenol, 4-bromo-2,6-di-tert-butyl phenol, 4-bromo-2-fluorophenol, 4-bromo-3,5-dimethylphenol, 4-cumylphenol, 4-cumylphenol, 4-bromophenol, 4-acetaminophen, 4-isopropylephenol, 5-(N-ethoxy) amino-o-cresol, 6-amino-m-cresol, 6-methoxy-2-naphthol, 6-chloro-5-amino-o-cresol, 6-bromo-2-naphthol, 7-bromo-2-naphthol, N,N-diethyl-3-aminophenol, thymol, thymolphthalein, thymol crystals, sudan IV, p-hydroxybenzoic acid, 4-methoxyphenol, 4-chloro-1-naphthol, 4-chloro-3,5-dimethylphenol, 4-chloro-3-ethylphenol, 3,5-dimethylphenol, 3,5-dimethoxyphenol, 3,5-dihydroxytoluene, 3,5-dimethylphenol, 3-aminophenol, 3-methyl salicylic acid, 4-amino-2-fluorophenol, 4-amino-3-cresol, 4-aminophenol, 4-fluorophenol, p-tert-butylphenol, p-tert-amylphenol, m-cresol, pentabromophenol, o-phenylphenol, o-hydroxyacetanilide, o-isopropylephenol, cardanol, 3-chloro-4-fluorophenol, 4,6-dinitro-o-sec-butylphenol, 4-amino-2,6-dichlorophenol and 4-(4-nitrobenzeneazo)-1-naphthol.


Further, the dihydric alcohol/phenol compound and its derivative comprise: 2,5-dimethyl-2,5-hexanediol, ethylene glycol bis (2-aminoethyl) tetraacetic acid, 1,4-butynediol, neopentyl glycol, polyvinyl butyral, phthalide, p-tolyldiethanolamine, 1,10-decanediol, 2,5-dimethyl-3-hexyne-2,5-diol, poly (neopentylene glycol succinate), 1,4-cyclohexanediol, 1,12-dodecanediol, (+) 2,3-pinanediol, 1,2-propylene glycol monomethyl ether acetate, colloidal dispersion, 1,4-phenyldimethanol, 1,4-cyclohexanedimethanol, 1,4-bis (2-hydroxyethoxy) benzene, 1,8-octanediol, 2,2,3-trimethyl-1,3-pentanediol, 2,2,4-trimethyl-1,3-pentanediol, 2-amino-1-[4-(methylthio) phenyl]-1,3-propanediol, 2-butyne-1,4-diol, 3,6-dithio-1,8-octanediol, N-phenyldiethanolamine, diglycolic acid, polybutylene terephthalate, polyethylene terephthalate, saligenin, ethylene glycol monostearate, isosorbide, 4,4-dihydroxy diphenyl sulfone, 2-bromopyrocatechol, 2,7-dihydroxynaphthalene, hydroquinone, 2,5-dichlorophen, 2,5-di-tert-butylhydroquinone, 2,6-dihydroxytoluene, 2,6-dihydroxynaphthalene, 1,4-benzenediol, 1,4-dimethoxy benzene, 1,4-cyclohexanediol, 1,5-dihydroxynaphthalene, 1,6-dibromo-2-naphthol, 1.3-dihydroxynaphthalene, 2,3-dihydroxynaphthalene, 3,4-dihydroxytoluene, 2,5-xylenol, 4-methylcatechol, 4-chlororesorcinol, catechol, 3,3′,5,5′-tetrabromobisphenol-A, 4-tert-butyl catechol, p-tert-butyl catechol, resorcinol, tert-butylhydroquinone, bisphenol-S, bisphenol-A epoxy resin, bisphenol-F resin, tetrabromobisphenol-A bis (2-ethoxy) ether, bromothymol blue, 4-(4-nitrobenzeneazo) resorcinol, 4,4-(1,3-dimethylbutylidene) diphenol, 4,4-(2-ethylhexylidene) diphenol and 4,6-dichlororesorcinol.


Further, the polyhydric alcohol/phenol compound and its derivative comprise: mannitol, octadecanol, tri (hydroxymethyl) propane, aluminum isopropoxide, triethanolamine hydrochloride (XZ), mannitol fermentation medium, D-sorbitol, pyridoxine hydrochloride, 4-tert-butylcyclohexanol, inositol, tri (hydroxymethyl) aminomethane, maltitol, triisopropanolamine, piperitol, sodium phytate, DL-menthol, maltol, erythritol, dipentaerythritol, pentaerythritol resin, pentaerythritol octahydrogen tetraphosphatepolyhydric, pentaerythritol tetra-(3,5-di-tert-butyl-4-hydroxyphenyl) propionate, polyethylene glycol, methoxypolyethylene glycol, polyvinyl alcohol 30,000-70,000, ammonium alcohol polyvinyl phosphate, xylitol, tri (hydroxymethyl) nitromethane, tripentaerythritol, triisopropanolamine cyclic borate, sorbitol, dulcitol, ethylene cellulose, phloroglucinol, pyrogallic acid, hydroxynaphthol blue disodium salt and tribromophenol.


Further, the fire-extinguishing composition comprises an auxiliary fire-extinguishing material.


Further, the auxiliary fire-extinguishing material comprises: chlorinated flame retardants, organophosphorus flame retardants, phosphorus-halogen flame retardants, nitrogen flame retardants, phosphorus-nitrogen flame retardants, inorganic flame retardants or any of their combinations.


Further, the fire-extinguishing composition comprises an additive and the content of the additive is 0.1-10%.


Further, the additive is a mold release agent, adhesive, catalyst or additive with other performances, such as: one or more of stearate, graphite, sodium silicate, phenolic resin, shellac, starch, dextrin, rubber, epoxy resin, acetal adhesive and hydroxypropyl methyl cellulose.


In addition to the substances listed above, all other organic or inorganic substances that can realize the foregoing functions may be used as substitutes of additives in the fire-extinguishing composition of the present invention.


Further, the components of the fire-extinguishing composition and their mass percentages are:

















the alcohol/phenol compound and its derivative
35%-90%



the auxiliary fire-extinguishing material
 5%-60%



the additive
 1%-10%.









Further, the components of the fire-extinguishing composition and their mass percentages are:

















the alcohol/phenol compound and its derivative
55%-90%



the auxiliary fire-extinguishing material
 5%-40%



the additive
 1%-5%.









The fire-extinguishing composition of the present invention adopts the following flame suppression mechanism:


During use, the pyrotechnic agent is used as a source of heat and a source of power. The heat released from ignition and combustion of the pyrotechnic agent makes the alcohol/phenol compound and its derivative react at a high temperature to generate free radical alkyl, free radical hydroxy, free radical hydrogen, and other active fire-extinguishing particles. These active fire-extinguishing particles react with one or more of O-, OH-, H-free radicals necessary for the chain combustion reaction, thereby cutting off the chain combustion reaction. Meanwhile, they take a synergistic interaction effect with the pyrotechnic agent to further raise the fire extinguishing efficiency of the fire extinguishing agent and greatly shorten the effective fire extinguishing time.


As compared with the existing thermal aerosol fire extinguishing agents, the fire-extinguishing composition of the present invention has the following advantages:

  • 1. The fire-extinguishing composition of the present invention reacts at a high temperature to generate various kinds of free radicals that can effectively put out a fire, to cut off the combustion reaction chain, and work together with the reaction products of the thermal aerosol generating agent to jointly play a fire extinguishing effect, further raise the fire extinguishing efficiency of the fire extinguishing agent and shorten the effective fire extinguishing time.
  • 2. The fire-extinguishing composition of the present invention makes use of the heat generated from the combustion of the aerosol generating agent to take the endothermic reaction fast, thereby absorbing the heat released from the combustion of the pyrotechnic agent and reducing the temperature at a nozzle of the fire extinguishing device. Therefore, the fire-extinguishing composition is safer, would not do harm to fire fighters and also avoids secondary fires.
  • 3. An aerosol fire extinguishing device adopting the fire-extinguishing composition of the present invention does not need a cooling system with a complex structure and a large volume, so it has the characteristics of a handy structure, a simple technological process and good economy.







DETAILED DESCRIPTION OF THE EMBODIMENTS

Below are embodiments of the present invention for illustrating a technical scheme for solving the technical problems in this application document and helping those skilled in the art understand the content of the present invention, however, the realization of the technical scheme of the present invention is not limited to these embodiments.


Take the fire-extinguishing composition of the present invention in proportion, add a specific amount of additive as required, use water as a solvent, pelletize by using a 20-mesh sieve, then add a specific amount of mold release agent, and after mixing the same, the mixture is sieved by a 15-mesh sieve and molded into a shape of ball, slice, strip, block or honeycomb through adopting pelleting, mould pressing, extruding or other processes; add 50 g of the mixture to a fire extinguishing unit filled with 50 g of a type K aerosol generating agent, and a fire extinguishing experiment is performed according to a fire extinguishing experiment model.


Comparative Example 1

Use a fire extinguishing device sample containing 50 g of a K salt type aerosol fire extinguishing agent and perform a fire extinguishing experiment according to the fire extinguishing experiment model.


Comparative Example 2

Use a fire extinguishing device sample containing 50 g of a type S aerosol fire extinguishing agent and perform a fire extinguishing experiment according to the fire extinguishing experiment model.


The fire extinguishing experiment model is an oil tray fire extinguishing experiment:


Experimental model: The oil tray is a round tray as mentioned in GA86-2009 8B (diameter: 570 mm; internal depth: 150 mm; approximate area: 0.25 m2).


Test method: Add 50 mm of water in the oil tray, add 22 mm of 93# motor gasoline, pre-burn for 1 min and then start fire extinguishing.


Evaluation standard: If no reburning takes place 1 min after the flame is put out and there is gasoline remaining in the oil tray, it is considered that fire extinguishing is successful. Experiment is performed for three times for each formula. Fire extinguishing effects, fire extinguishing time and nozzle temperatures are recorded. The experimental results are shown in Tables 1-6:









TABLE 1







Comparison of fire extinguishing experimental results of single alcohol/phenol component











Embodiment component content (mass percentage %)
Comparative
Comparative


















Component
1
2
3
4
5
6
7
8
9
example 1
example 2





















Commercial













type K aerosol













Commercial













type S aerosol













Benzhydrol
100












2,6-di-tert-

93











butyl-p-cresol













2-naphthol


95










1-naphthol



92









Thymol




96








4-methoxy





96







phenol













4-aminophenol






98






p-hydroxy







90





benzoic acid













Octadecanol








94




Magnesium

2
2
4
2
2
1
5
2




stearate













Hydroxypropyl

5
3
4
2
2
1
5
4




methyl cellulose













Nozzle
716
669
802
813
704
598
812
657
713
1211
1305


temperature ° C.













8B fire extinguishing
Full
Full
Full
2 Extinc-
Full
Full
Full
Full
Full
No
No


performance
Extinc-
Extinc-
Extinc-
tions
Extinc-
Extinc-
Extinc-
Extinc-
Extinc-
Extinc-
Extinc-



tions
tions
tions
out of 3
tions
tions
tions
tions
tions
tions
tions


Fire extinguishing
4
3
5
4
5
3
5
5
5




time s
















TABLE 2







Comparison of various components and ingredients and comparison of fire extinguishing test results thereof











Embodiment component content (mass percentage)
Comparative
Comparative
















Component
10
11
12
13
14
15
16
example 1
example e2



















Commercial











type K aerosol











Commercial











type S aerosol











4-aminophenol
50



43

45




Benzhydrol

66









2,6-di-tert-


70








butyl-p-cresol











2-naphthol



41







1-naphthol



35
42






Thymol





90





4-methoxyphenol






48




Melamine
46
30









polyphosphatee











Aluminum


26








hydroxide











Magnesium



20







hydroxide











Ammonium




14






chloride











Melamine





6





cyanurate











Zinc borate






5




Magnesium
2
2
2
2
0.5
2
1




stearate











Hydroxypropyl
2
2
2
2
0.5
2
1




methyl cellulose











Nozzle
467
566
590
602
654
588
634
1211
1305


temperature ° C.











Fire extinguishing
2 Extinc-
Full
Full
Full
Full
Full
Full
No
No


performance
tions
Extinc-
Extinc-
Extinc-
Extinc-
Extinc-
Extinc-
Extinc-
Extinc-



out of 3
tions
tions
tions
tions
tions
tions
tions
tions


Fire extinguishing
5
3
5
5
5
3
4




time s
















TABLE 3







Comparison of fire extinguishing experimental results of single alcohol/phenol component











Embodiment component content (mass percentage %)
Comparative
Comparative

















Component
17
18
19
20
21
22
23
24
example 1
example 2




















Commercial












type K aerosol












Commercial












type S aerosol












Polyvinyl butyral
96











1,12-dodecane

96










diol












4,4 dihydroxy


96









diphenyl sulfone












2,5-di-tert-



96








butylhydroquinone












Catechol




96







Resorcinol





96






1,4-benzenediol






96





p-tert-butyl







96




catechol












Magnesium
2
3
2
2
1
2
2
0.5




stearate












Hydroxypropyl
2
1
2
2
3
2
2
3.5




methyl cellulose












Nozzle
682
701
812
765
689
701
713
798
1211
1305


temperature ° C.












8B fire extinguishing
Full
Full
Full
2 Extinc-
Full
Full
Full
Full
No
No


performance
Extinc-
Extinc-
Extinc-
tions
Extinc-
Extinc-
Extinc-
Extinc-
Extinc-
Extinc-



tions
tions
tions
out of 3
tions
tions
tions
tions
tions
tions


Fire extinguishing
4
5
4
5
3
5
5
5




time s
















TABLE 4







Comparison of various components and ingredients and comparison of fire extinguishing test results thereof











Embodiment component content (mass percentage %)
Comparative
Comparative

















Component
25
26
27
28
29
30
31
32
example 1
example 2




















Commercial












type K aerosol












Commercial












type S aerosol












Polyvinyl
55











butyral












1,12-dodecane

66










diol












4,4 dihydroxy


72









diphenyl sulfone












2,5-di-tert-



78


45





butylhydroquinone












Catechol




45







Resorcinol




35
85






1,4-benzenediol






45





p-tert-butyl







90




catechol












Melamine
41
30





5




polyphosphate












Aluminum


24









hydroxide












Magnesium



18








hydroxide












Ammonium




16







chloride












Melamine





11






cyanurate












Zinc borate






5





Magnesium
1
2
2
2
2
2
2
2




stearate












Hydroxypropyl
3
2
2
2
2
2
3
3




methyl cellulose












Nozzle
498
455
670
697
652
675
686
754
1211
1305


temperature ° C.












8B fire extinguishing
Full
Full
2 Extinc-
Full
Full
Full
2 Extinc-
Full
No
No


performance
Extinc-
Extinc-
tions
Extinc-
Extinc-
Extinc-
tions
Extinc-
Extinc-
Extinc-



tions
tions
out of 3
tions
tions
tions
out of 3
tions
tions
tions


Fire extinguishing
4
5
4
4
3
5
5
5




time s
















TABLE 5







Comparison of fire extinguishing experimental results of single alcohol/phenol component











Embodiment component content (mass percentage %)
Comparative
Comparative

















Component
33
34
35
36
37
38
39
40
example 1
example 2




















Commercial












type K aerosol












Commercial












type S aerosol












Mannitol
96











Triethanolamine

96










hydrochloride












Pyridoxine


96









hydrochloride












Inositol



96








Tri(hydroxy-




96







methyl)amino-












methane












Sorbitol





96






Ethylene






96





cellulose












Pyrogallic







96




acid












Magnesium
2
2
2
2
2
2
2
2




stearate












Hydroxypropyl
2
2
2
2
2
2
2
2




methyl cellulose












Nozzle
817
765
689
704
764
657
671
703
1211
1305


temperature ° C.












8B fire extinguishing
Full
Full
Full
2 Extinc-
Full
Full
Full
Full
No
No


performance
Extinc-
Extinc-
Extinc-
tions
Extinc-
Extinc-
Extinc-
Extinc-
Extinc-
Extinc-



tions
tions
tions
out of 3
tions
tions
tions
tions
tions
tions


Fire extinguishing
4
5
4
4
3
5
5
5




time s
















TABLE 6







Comparison of various components and ingredients and comparison of fire extinguishing test results thereof











Embodiment component content (mass percentage %)
Comparative
Comparative

















Component
41
42
43
44
45
46
47
48
example 1
example 2




















Commercial












type K aerosol












Commercial












type S aerosol












Mannitol
56











Octadecanol

35










Triethanolamine


72









hydrochloride












Pyridoxine



45








hydrochloride












Inositol

30


82







Tri(hydroxyl





84






methyl)amino-












methane












Sorbitol






90





Pyrogallic



31



90




acid












Melamine
44
31










polyphosphate












Aluminum


24









hydroxide












Magnesium



20








hydroxide












Ammonium




14







chloride












Melamine





12






cyanurate












Zinc borate






6
5




Magnesium

2
2
2
2
2
2
2




stearate












Hydroxypropyl

2
2
2
2
2
2
3




methyl cellulose












Nozzle
602
589
576
632
675
704
679
652
1211
1305


temperature ° C.












8B Fire extinguishing
Full
Full
Full
Full
Full
Full
Full
Full
No
No


performance
Extinc-
Extinc-
Extinc-
Extinc-
Extinc-
Extinc-
Extinc-
Extinc-
Extinc-
Extinc-



tions
tions
tions
tions
tions
tions
tions
tions
tions
tions


Fire extinguishing
4
5
4
4
3
5
5
5




time s









The foregoing embodiments are merely explanations to the preferred schemes of the present invention, and are not the limitation to the present invention. All changes and modifications to the foregoing embodiments within the essential spirit scope of the present invention should fall within the scope of protection of the claims of the present application.

Claims
  • 1. An aerosol fire-extinguishing composition comprising: i) 35%-90% by mass of one or more of a compound selected from the group consisting of:3-aminobenzyl alcohol, 2,3,5-trimethylphenol, magnesium ethoxide, benzilic acid, benzhydrol, 4-hydroxy-3-methoxybenzyl alcohol, octadecanol, 2-(4-hydroxyphenyl)ethanol, 2-nitrobenzyl alcohol, 2-(β-ethoxy) amino-5-nitro, phenoxyethanol, 2,2-dimethyl-1-propanol, 1-adamantanol, lithium tert-butoxide, cholesterol, 2,6,7-trioxa-1-phosphabicyclo (2,2,2) octane-4-methanol-1 (pentaerythritol octahydrogen tetraphosphate), 3-(3,5-di-tert-butyl-4-hydroxyphenyl) propanoic acid octadecyl ester, 5-indanol, β-sitosterol, piroctone olamine, 4-methylbenzyl alcohol, sodium methoxide, sodium trimethylsilanolate, triphenylcarbinol, potassium tert-butoxide, sodium tert-butoxide, tetramethyl piperidinol, tebuconazole, ethanolamine hydrochloride, potassium ethoxide, sodium glycollate, 2.3-dimethylphenol, 2.5-dimethylphenol, 2-amino-5-chlorophenol, 2-amino-5-nitrophenol, 2,6-dichlorophenol, 2-aminophenol, 2,4,6-trimethylphenol, 2,4,6-tribromophenol, 2,4-di-tert-butyl-6-(5-chloro-2H-benzotriazole-2-yl)phenol, 2,4-di-tert-butylphenol, 2,4-di-tert-butylphenol, 2-phenylphenol, 2,5-dichlorothiophenol, 2,6-di-tert-butyl-p-cresol, 2,6-tert-butyl-4-cresol, 2-methyl-3-nitrophenol, 2-methyl-5-aminophenol, 2-chloro-4-fluorophenol, 2-chloro-4-methoxyphenol, 2-chloro-4-bromophenol, 2-naphthol, 2-hydroxypyridine, 2-tert-butyl-5-cresol, 2-bromo-4-cresol, 2-bromo-p-cresol, 1-amino-7-naphthol, 1-naphthol, 1-bromo-2-naphthol, 2-(2H-benzotriazole-2-yl)-4,6-di-tert-pentylphenol, 2-(5-bromo-2-pyridine)azo-5-(diethylamino)phenol, 2,2′-diphenol, 2,2′-binaphthol, 2,2-methylenebis[6-benzotriazole-2-yl]-4-tert-octylphenol, 2,3,5-trimethylphenol, 2,3,6-trimethylphenol, 2,3-dichlorophenol, 2-nitroso-1-naphthol, 2-ethoxy-5-(1-propenyl) phenol, 2-ethoxyphenol, 2-isopropylephenol, 3,4-xylenol, 3,4-dimethylphenol, 3,4-dimethoxyphenol, 4-bromo-2,6-di-tert-butyl phenol, 4-bromo-2-fluorophenol, 4-bromo-3,5-dimethylphenol, 4-cumylphenol, 4-bromophenol, 4-acetaminophen, 4-isopropylephenol, 5-(N-ethoxy) amino-o-cresol, 6-amino-m-cresol, 6-methoxy-2-naphthol, 6-chloro-5-amino-o-cresol, 6-bromo-2-naphthol, 7-bromo-2-naphthol, N,N-diethyl-3-aminophenol, thymol, thymolphthalein, thymol crystals, sudan IV, p-hydroxybenzoic acid, 4-methoxyphenol, 4-chloro-1-naphthol, 4-chloro-3,5-dimethylphenol, 4-chloro-3-ethylphenol, 3,5-dimethylphenol, 3,5-dimethoxyphenol, 3,5-dihydroxytoluene, 3,5-dimethylphenol, 3-aminophenol, 3-methyl salicylic acid, 4-amino-2-fluorophenol, 4-amino-3-cresol, 4-aminophenol, 4-fluorophenol, p-tert-butylphenol, p-tert-amylphenol, m-cresol, pentabromophenol, o-phenylphenol, o-hydroxyacetanilide, o-isopropylephenol, cardanol, 3-chloro-4-fluorophenol, 4,6-dinitro-o-sec-butylphenol, 4-amino-2,6-dichlorophenol, 4-(4-nitrobenzeneazo)-1-naphthol;ii) 5%-60% by mass of an auxiliary fire-extinguishing material; andiii) 1%-10% by mass of an additive,wherein the auxiliary fire-extinguishing material is one or more of: a chlorinated flame retardant, an organophosphorus flame retardant, a phosphorus-halogen flame retardant, a nitrogen flame retardant, a phosphorus-nitrogen flame retardant, and an inorganic flame retardant.
  • 2. The aerosol fire-extinguishing composition according to claim 1, wherein the additive is one or more of stearate, graphite, sodium silicate, phenolic resin, shellac, starch, dextrin, rubber, epoxy resin, acetal adhesive and hydroxypropyl methyl cellulose.
  • 3. The aerosol fire-extinguishing composition according to claim 1, wherein the composition comprises: a) 55%-90% by mass of the one or more of compounds of i);b) 5%-40% by mass of the auxiliary fire-extinguishing material; andc) 1%-5% by mass of the additive.
Priority Claims (1)
Number Date Country Kind
2014 1 0014330 Jan 2014 CN national
PCT Information
Filing Document Filing Date Country Kind
PCT/CN2015/074045 3/11/2015 WO 00
Publishing Document Publishing Date Country Kind
WO2015/104007 7/16/2015 WO A
US Referenced Citations (15)
Number Name Date Kind
4665993 Balassa May 1987 A
5520826 Reed, Jr. et al. May 1996 A
8257607 Johnson Sep 2012 B1
8778213 Guo et al. Jul 2014 B2
8871110 Guo et al. Oct 2014 B2
9662522 Liu May 2017 B2
20020137875 Reed et al. Sep 2002 A1
20030010508 Greiner Jan 2003 A1
20090069496 Sortwell Mar 2009 A1
20130221264 Guo et al. Aug 2013 A1
20140183399 Yao et al. Jul 2014 A1
20140374641 Liu et al. Dec 2014 A1
20160332015 Zhang et al. Nov 2016 A1
20160332016 Yao et al. Nov 2016 A1
20170043196 Wu et al. Feb 2017 A1
Foreign Referenced Citations (20)
Number Date Country
102179027 Sep 2011 CN
102824715 Dec 2012 CN
102861409 Jan 2013 CN
102949802 Mar 2013 CN
102949803 Mar 2013 CN
102993626 Mar 2013 CN
103111035 May 2013 CN
103170082 Jun 2013 CN
103736236 Apr 2014 CN
103736237 Apr 2014 CN
103736239 Apr 2014 CN
103785130 May 2014 CN
20060092192 Aug 2006 KR
WO 2009032587 Mar 2009 WO
WO 2012034492 Mar 2012 WO
2012154768 Nov 2012 WO
WO 2015104004 Jul 2015 WO
WO 2015104005 Jul 2015 WO
WO 2015104006 Jul 2015 WO
WO 2015104007 Jul 2015 WO
Non-Patent Literature Citations (14)
Entry
English abstract of KR 20060092192 A (2006).
PCT/CN2015/074033 English Translation of the International Preliminary Report on Patentability dated Jul. 19, 2016 entitled “Fire Extinguishing Composition Comprising Carboxylic Acid Derivative.”
PCT/CN2015/074033 English Translation of the International Search Report dated May 29, 2015 entitled “Fire Extinguishing Composition Comprising Carboxylic Acid Derivative.”
PCT/CN2015/074033 English Translation of the Written Opinion dated May 29, 2015 entitled “Fire Extinguishing Composition Comprising Carboxylic Acid Derivative.”
PCT/CN2015/074043 English Translation of the International Preliminary Report on Patentability dated Jul. 19, 2016 entitled “Fire Extinguishing Composition Comprising Heterocyclic Compounds.”
PCT/CN2015/074043 English Translation of the International Search Report dated May 27, 2015 entitled “Fire Extinguishing Composition Comprising Heterocyclic Compounds.”
PCT/CN2015/074043 English Translation of the Written Opinion dated May 27, 2015 entitled “Fire Extinguishing Composition Comprising Heterocyclic Compounds.”
PCT/CN2015/074044 English Translation of the International Preliminary Report on Patentability dated Jul. 19, 2016 entitled “Fire Extinguishing Composition Comprising Aldoketones Compound.”
PCT/CN2015/074044 English Translation of the International Search Report dated May 29, 2015 entitled “Fire Extinguishing Composition Comprising Aldoketones Compound.”
PCT/CN2015/074044 English Translation of the Written Opinion dated May 29, 2015 entitled “Fire Extinguishing Composition Comprising Aldoketones Compound.”
PCT/CN2015/074045 English Translation of the International Preliminary Report on Patentability dated Jul. 19, 2016 entitled “Fire Extinguishing Composition Comprising Alcohol Phenol Compound and Derivative Thereof.”
PCT/CN2015/074045 English Translation of the International Search Report dated Jun. 17, 2015 entitled “Fire Extinguishing Composition Comprising Alcohol Phenol Compound and Derivative Thereof.”
PCT/CN2015/074045 English Translation of the Written Opinion dated Jun. 17, 2015 entitled “Fire Extinguishing Composition Comprising Alcohol Phenol Compound and Derivative Thereof.”
Chemspider, The free chemical database, “Benzophenone”, Oct. 23, 2012.
Related Publications (1)
Number Date Country
20160332014 A1 Nov 2016 US