WO2011078849A1 - Fire retardant composition and fire suppression apparatus - Google Patents

Fire retardant composition and fire suppression apparatus Download PDF

Info

Publication number
WO2011078849A1
WO2011078849A1 PCT/US2009/069145 US2009069145W WO2011078849A1 WO 2011078849 A1 WO2011078849 A1 WO 2011078849A1 US 2009069145 W US2009069145 W US 2009069145W WO 2011078849 A1 WO2011078849 A1 WO 2011078849A1
Authority
WO
WIPO (PCT)
Prior art keywords
particles
recited
flame retardant
fire
substrate
Prior art date
Application number
PCT/US2009/069145
Other languages
French (fr)
Inventor
Treese Hugener-Campbell
Jose L. Santana
Original Assignee
Utc Fire & Security Corporation
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Utc Fire & Security Corporation filed Critical Utc Fire & Security Corporation
Priority to PCT/US2009/069145 priority Critical patent/WO2011078849A1/en
Publication of WO2011078849A1 publication Critical patent/WO2011078849A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A62LIFE-SAVING; FIRE-FIGHTING
    • A62DCHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
    • A62D1/00Fire-extinguishing compositions; Use of chemical substances in extinguishing fires
    • A62D1/0007Solid extinguishing substances
    • A62D1/0014Powders; Granules
    • AHUMAN NECESSITIES
    • A62LIFE-SAVING; FIRE-FIGHTING
    • A62DCHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
    • A62D1/00Fire-extinguishing compositions; Use of chemical substances in extinguishing fires
    • A62D1/0028Liquid extinguishing substances
    • A62D1/005Dispersions; Emulsions

Definitions

  • Inorganic salts such as those composed of phosphate anions are known and used to extinguish or retard thermal events, such as fires.
  • particles of the monoammonium phosphate may be included in a fire extinguisher that projects the material onto the fire to be extinguished.
  • additives may be combined or added to the particles of monoammonium phosphate to facilitate the use or flow thereof.
  • additive particles of silica may aid the flow of the material and other types of inorganic salts, such as ammonium sulfate may be added to the mixture.
  • An exemplary fire retardant composition for use in a fire suppression apparatus includes a powdered material having a plurality of substrate particles and flame retardant particles disposed on surfaces of the plurality of substrate particles.
  • An example fire suppression apparatus includes a container and a fire retardant material within the container.
  • the fire retardant material includes a powdered material having a plurality of substrate particles and flame retardant particles dispersed on surfaces of the plurality of substrate particles.
  • An exemplary method of producing a fire retardant composition for use in a fire suppression apparatus includes depositing flame retardant particles onto surfaces of a plurality of substrate particles of a powdered material.
  • Figure 1 illustrates a powdered material having a fire retardant composition.
  • Figure 2 illustrates a fire suppression apparatus that includes the powdered material illustrated in Figure 1.
  • Figure 1 illustrates selected portions of an example fire retardant powdered material 20 for use in a fire suppression apparatus, such as a fire extinguisher.
  • the powdered material 20 is of a composition that utilizes a flame retardant material dispersed mainly on the surface of a substrate particle, such as an additive particle.
  • the powdered material 20 thereby utilizes less flame retardant material than prior known compositions and is therefore more efficient in extinguishing a flame.
  • the powdered material 20 includes a plurality of substrate particles 22 that each includes flame retardant particles 24 disposed on surfaces 26 of the substrate particles 22.
  • the substrate particles 22 may be selected among mica, silica, diatomaceous earth, and combinations thereof. That is, all of the substrate particles 22 may be one of the designated types of materials or a mixture of any two or more of these materials.
  • the substrate particles 22 may have a surface area of around 400 m 2 /g or less.
  • the relatively high surface area provides a corresponding greater surface to deposit flame retardant particles 24 that will in turn higher exposure to a flame.
  • a greater amount of the flame retardant particles 24 are exposed to the flame than if the flame retardant particles were provided as individual particles of lower surface area rather than deposited onto the substrate particles 22.
  • the disclosed arrangement of the powdered material 20 provides a more efficient and effective flame extinguishing property.
  • the substrate particles 22 may be selected to have an average particle size within a desired range to provide a targeted surface area.
  • a substrate particle 22 may have an average particle size of up to about 50 micrometers.
  • the average particle size may be about 1-20 micrometers. If the substrate particles 22 are mica, an average particle size toward the higher end of the range at approximately 20 micrometers may have a surface area of approximately 5 m 2 /g. On the other hand, an average particle size toward the other end of a given range at one micrometer for a particle of silica may have an average surface area of around 350 m 2 /g.
  • the flame retardant particles 24 may additionally deposit between the layered sheets of the material and also on the outer surfaces of the material. That is, for any given type of substrate particle 22, the flame retardant particles may be deposited primarily on the outer surfaces or also within pores or interlayer between sheets if the given type of substrate particle 22 includes such features.
  • the flame retardant particles may be particles of monoammonium phosphate (NH 4 H 2 PO 4 ).
  • the monoammonium phosphate may be deposited onto the substrate particles 22 in any of a variety of different techniques.
  • monoammonium phosphate is soluble in water and may thereby be mixed with water or other type of carrier liquid to form a solution.
  • Other additives may be added to the solution to openly facilitate flow of the fire retardant composition or in part other properties thereto.
  • silica particles may be added to the composition mixture solution as a flow aid. The substrate particles 22 may then be added to the solution and mixed therewith.
  • the solution infiltrates any pores in the substrate particles 22 or in the case of a layered material between the sheets.
  • infiltration of the pores or sheets may depend upon chemical interactions between the solution and the substrate particles 22.
  • the mixture may then be stirred for a desired amount of time, such as 30 minutes before removal of the carrier liquid.
  • the carrier liquid may be removed by vacuum and/or elevated temperatures.
  • the carrier liquid is removed through rotary evaporation such that the mixture is continually mixed during removal.
  • the mixture may be spray dried in a known manner to deposit the flame retardant particles 24 onto the surfaces of the substrate particles 22.
  • the spray drying may include providing two feeds that are blown into a heated vacuum chamber.
  • One of the feeds may be the solution of the carrier liquid and the monoammonium phosphate and any other additives that will be used and other feed may be the substrate particles 22.
  • the liquid carrier evaporates when blown into the chamber, the remaining monoammonium phosphate deposits onto the substrate particles 22 to thereby form the powdered material 20.
  • temperatures of around 100-120°C may be used. Of course, the selected temperature may depend upon the type of carrier liquid that is used.
  • Additional methods of preparation include heating the monoammonium phosphate and the rapidly mixing a substrate and additive while keeping the monoammonium phosphate in the molten state.
  • a further method of preparation includes the high friction mixing of the monoammonium phosphate salt onto to the substrate and additive components. High friction mixing would take advantage of the much lower melting point of the monoammonium phosphate ( ⁇ 190°C) and ideally disperse the phosphate salt onto the substrate and additive particles as described in the other methods of preparation.
  • the composition of the flame retardant particle 24 relative to the total combined weight of the flame retardant particles 24 and the substrate particles 22 may be adjusted as desired during the fabrication process.
  • the composition of the powdered material 20 may include up to about 45 wt.% of the flame retardant particles 24.
  • the composition may include 15-40 wt.% of the flame retardant particles 24 or even 20-24 wt.%.
  • flame retardant such as monoammonium phosphate are commonly used in much higher percentages, the disclosed examples and fabrication techniques allow effective use of lower amounts of the monoammonium phosphate.
  • the amount of flame retardant particles 24 and the final composition depends upon the amount used in the solution to make the powdered material 20.
  • a slightly higher amount relative to weight percent may be required in the solution than is desired in the final composition due to the loss of some of the monoammonium phosphate in the process.
  • the amount of monoammonium phosphate in the preparation solution may correspond closely to the amount in the final product.
  • there may be some variation in the process that may or may not influence the final composition.
  • rotary evaporation of an amount of about 26 wt.% of the monoammonium phosphate relative to the total combined amount of monoammonium phosphate and substrate particles in the mixture was used to produce a final composition of the powdered material 20 that had approximately 24 wt.% of the flame retardant particles 24.
  • the process may be more efficient such that the mixture more closely corresponds to the amount of flame retardant particles in the final composition.
  • the powdered material 20 may undergo a grinding step after removal of the carrier liquid. For instance, the grinding may break up any agglomerates that formed during the fabrication process. In one example, the powdered material 20 may be ground for a relatively short time such as five minutes to break up any agglomerates and thereby avoid forming other agglomerates that generally broaden the particle size distribution.
  • Figure 2 illustrates an example fire suppression apparatus 40 that the powdered material 20 may be used within.
  • the fire suppression apparatus 40 includes a container 42 and the powdered material 20 within the container as a fire retardant material.
  • the fire retardant material includes the plurality of substrate particles 22 and the flame retardant particles 24 disposed on surfaces of the substrate particles 22.
  • a release tube 44 extends within the container 42 and includes an opening 46 near the bottom of the container 42.
  • the release tube 44 extends upwards from the end 46 and terminates at a nozzle section 48 for releasing the flame retardant material.
  • the powdered material 20 flows upwards through the release tube 44 and opening 46 towards the nozzle 48.
  • the fire retardant material may be pressurized such that a user may manually open the nozzle 48 to release a discharge or spray of the fire retardant material.
  • the fire suppression apparatus 40 shown in the illustrated example may also include other features or components and is not limited to the particular arrangement shown.
  • the powdered material 20 may be used in other types of fire extinguishing devices or arrangements that are not specifically shown here.

Abstract

A fire retardant composition for use in a fire suppression apparatus includes a powdered material having a plurality of substrate particles and flame retardant particles disposed on surfaces of the plurality of substrate particles.

Description

FIRE RETARDANT COMPOSITION
AND FIRE SUPPRESSION APPARATUS
BACKGROUND
[0001] Inorganic salts, such as those composed of phosphate anions are known and used to extinguish or retard thermal events, such as fires. For instance, particles of the monoammonium phosphate may be included in a fire extinguisher that projects the material onto the fire to be extinguished. Various types of additives may be combined or added to the particles of monoammonium phosphate to facilitate the use or flow thereof. For instance, additive particles of silica may aid the flow of the material and other types of inorganic salts, such as ammonium sulfate may be added to the mixture.
SUMMARY
[0002] An exemplary fire retardant composition for use in a fire suppression apparatus includes a powdered material having a plurality of substrate particles and flame retardant particles disposed on surfaces of the plurality of substrate particles.
[0003] An example fire suppression apparatus includes a container and a fire retardant material within the container. The fire retardant material includes a powdered material having a plurality of substrate particles and flame retardant particles dispersed on surfaces of the plurality of substrate particles.
[0004] An exemplary method of producing a fire retardant composition for use in a fire suppression apparatus includes depositing flame retardant particles onto surfaces of a plurality of substrate particles of a powdered material.
[0005] The various features and advantages of disclosed examples will become apparent to those skilled in the art from the following detailed description. The drawings that accompany the detailed description can be briefly described as follows.
BRIEF DESCRIPTION OF THE DRAWINGS
[0006] Figure 1 illustrates a powdered material having a fire retardant composition.
[0007] Figure 2 illustrates a fire suppression apparatus that includes the powdered material illustrated in Figure 1. DETAILED DESCRIPTION
[0008] Figure 1 illustrates selected portions of an example fire retardant powdered material 20 for use in a fire suppression apparatus, such as a fire extinguisher. In this case, the powdered material 20 is of a composition that utilizes a flame retardant material dispersed mainly on the surface of a substrate particle, such as an additive particle. As will be described in further detail, the powdered material 20 thereby utilizes less flame retardant material than prior known compositions and is therefore more efficient in extinguishing a flame.
[0009] In the illustrated example, the powdered material 20 includes a plurality of substrate particles 22 that each includes flame retardant particles 24 disposed on surfaces 26 of the substrate particles 22.
[0010] The following examples will illustrate a few options for selecting the type of flame retardant particles 24 and substrate particles 22. However, it is to be understood that this disclosure is not limited to the examples herein and, given this disclosure, one of ordinary skill in the art will be able to select other types of materials to suit their particular needs. In this case, the substrate particles 22 may be selected among mica, silica, diatomaceous earth, and combinations thereof. That is, all of the substrate particles 22 may be one of the designated types of materials or a mixture of any two or more of these materials. To give examples provide the benefit of having a relatively high surface area for deposition of the frame retardant particles 24. For instance, the substrate particles 22 may have a surface area of around 400 m2/g or less. The relatively high surface area provides a corresponding greater surface to deposit flame retardant particles 24 that will in turn higher exposure to a flame. In comparison, a greater amount of the flame retardant particles 24 are exposed to the flame than if the flame retardant particles were provided as individual particles of lower surface area rather than deposited onto the substrate particles 22. In this regard, the disclosed arrangement of the powdered material 20 provides a more efficient and effective flame extinguishing property.
[0011] In a further example, the substrate particles 22 may be selected to have an average particle size within a desired range to provide a targeted surface area. For instance, a substrate particle 22 may have an average particle size of up to about 50 micrometers. In a further example, the average particle size may be about 1-20 micrometers. If the substrate particles 22 are mica, an average particle size toward the higher end of the range at approximately 20 micrometers may have a surface area of approximately 5 m2/g. On the other hand, an average particle size toward the other end of a given range at one micrometer for a particle of silica may have an average surface area of around 350 m2/g. Although such smaller particles have a greater surface area, there may be other considerations in selecting an appropriate particle size for a particle use such as flow characteristics of the particles. Additionally, for a layered type of substrate such as mica, the flame retardant particles 24 may additionally deposit between the layered sheets of the material and also on the outer surfaces of the material. That is, for any given type of substrate particle 22, the flame retardant particles may be deposited primarily on the outer surfaces or also within pores or interlayer between sheets if the given type of substrate particle 22 includes such features.
[0012] In the above examples, the flame retardant particles may be particles of monoammonium phosphate (NH4H2PO4). In this case, the monoammonium phosphate may be deposited onto the substrate particles 22 in any of a variety of different techniques. For instances, monoammonium phosphate is soluble in water and may thereby be mixed with water or other type of carrier liquid to form a solution. Other additives may be added to the solution to openly facilitate flow of the fire retardant composition or in part other properties thereto. For instance, silica particles may be added to the composition mixture solution as a flow aid. The substrate particles 22 may then be added to the solution and mixed therewith. Such step that the solution infiltrates any pores in the substrate particles 22 or in the case of a layered material between the sheets. Of course, infiltration of the pores or sheets may depend upon chemical interactions between the solution and the substrate particles 22. The mixture may then be stirred for a desired amount of time, such as 30 minutes before removal of the carrier liquid. As an example, the carrier liquid may be removed by vacuum and/or elevated temperatures. In one example, the carrier liquid is removed through rotary evaporation such that the mixture is continually mixed during removal. In another example technique, the mixture may be spray dried in a known manner to deposit the flame retardant particles 24 onto the surfaces of the substrate particles 22. For instance, the spray drying may include providing two feeds that are blown into a heated vacuum chamber. One of the feeds may be the solution of the carrier liquid and the monoammonium phosphate and any other additives that will be used and other feed may be the substrate particles 22. As the liquid carrier evaporates when blown into the chamber, the remaining monoammonium phosphate deposits onto the substrate particles 22 to thereby form the powdered material 20. In either of the above exemplary techniques, temperatures of around 100-120°C may be used. Of course, the selected temperature may depend upon the type of carrier liquid that is used. [0013] Additional methods of preparation include heating the monoammonium phosphate and the rapidly mixing a substrate and additive while keeping the monoammonium phosphate in the molten state. A further method of preparation includes the high friction mixing of the monoammonium phosphate salt onto to the substrate and additive components. High friction mixing would take advantage of the much lower melting point of the monoammonium phosphate (~190°C) and ideally disperse the phosphate salt onto the substrate and additive particles as described in the other methods of preparation.
[0014] The composition of the flame retardant particle 24 relative to the total combined weight of the flame retardant particles 24 and the substrate particles 22 may be adjusted as desired during the fabrication process. As an example, the composition of the powdered material 20 may include up to about 45 wt.% of the flame retardant particles 24. In further examples, the composition may include 15-40 wt.% of the flame retardant particles 24 or even 20-24 wt.%. Whereas flame retardant such as monoammonium phosphate are commonly used in much higher percentages, the disclosed examples and fabrication techniques allow effective use of lower amounts of the monoammonium phosphate. In some cases, the amount of flame retardant particles 24 and the final composition depends upon the amount used in the solution to make the powdered material 20. For instance, a slightly higher amount relative to weight percent may be required in the solution than is desired in the final composition due to the loss of some of the monoammonium phosphate in the process. In other examples, the amount of monoammonium phosphate in the preparation solution may correspond closely to the amount in the final product. Thus, there may be some variation in the process that may or may not influence the final composition. In one example rotary evaporation of, an amount of about 26 wt.% of the monoammonium phosphate relative to the total combined amount of monoammonium phosphate and substrate particles in the mixture was used to produce a final composition of the powdered material 20 that had approximately 24 wt.% of the flame retardant particles 24. In other techniques, such as spray drying, the process may be more efficient such that the mixture more closely corresponds to the amount of flame retardant particles in the final composition.
[0015] In the above examples, the powdered material 20 may undergo a grinding step after removal of the carrier liquid. For instance, the grinding may break up any agglomerates that formed during the fabrication process. In one example, the powdered material 20 may be ground for a relatively short time such as five minutes to break up any agglomerates and thereby avoid forming other agglomerates that generally broaden the particle size distribution. [0016] Figure 2 illustrates an example fire suppression apparatus 40 that the powdered material 20 may be used within. In this example, the fire suppression apparatus 40 includes a container 42 and the powdered material 20 within the container as a fire retardant material. As described above, the fire retardant material includes the plurality of substrate particles 22 and the flame retardant particles 24 disposed on surfaces of the substrate particles 22. In this case, a release tube 44 extends within the container 42 and includes an opening 46 near the bottom of the container 42. The release tube 44 extends upwards from the end 46 and terminates at a nozzle section 48 for releasing the flame retardant material. In operation, the powdered material 20 flows upwards through the release tube 44 and opening 46 towards the nozzle 48. In this regard, the fire retardant material may be pressurized such that a user may manually open the nozzle 48 to release a discharge or spray of the fire retardant material. It is to be understood that the fire suppression apparatus 40 shown in the illustrated example may also include other features or components and is not limited to the particular arrangement shown. In this regard, the powdered material 20 may be used in other types of fire extinguishing devices or arrangements that are not specifically shown here.
[0017] The preceding description is exemplary rather than limiting in nature. Variations and modifications to the disclosed examples may become apparent to those skilled in the art that do not necessarily depart from the scope of legal protection given to this invention, which can only be determined by studying the following claims.

Claims

CLAIMS What is claimed is:
1. A fire retardant composition for use in a fire suppression apparatus, comprising:
a powdered material having a plurality of substrate particles; and flame retardant particles dispersed on surfaces of the plurality of substrate particles.
2. The fire retardant composition as recited in claim 1, wherein the plurality of substrate particles are mica.
3. The fire retardant composition as recited in claim 1, wherein the flame retardant particles are monoammonium phosphate.
4. The fire retardant composition as recited in claim 1, wherein the substrate particles are mica and the flame retardant particles are monoammonium phosphate.
5. The fire retardant composition as recited in claim 4, wherein the mica has an average particle size of up to 50 micrometers.
6. The fire retardant composition as recited in claim 5, wherein the average particle size is 1-20 micrometers.
7. The fire retardant composition as recited in claim 1, including 5-45 wt.% of the flame retardant particles relative to a total combined weight of the flame retardant particles and the plurality of substrate particles.
8. The fire retardant composition as recited in claim 7, including 15-40 wt.% of the flame retardant particles relative to the total combined weight.
9. The fire retardant composition as recited in claim 8, including 20-24 wt.% of the flame retardant particles relative to the total combined weight.
10. The fire retardant composition as recited in claim 1, wherein the plurality of substrate particles are selected from a group consisting of mica, silica, diatomaceous earth, and combinations thereof.
11. The fire retardant composition as recited in claim 1 , wherein the plurality of substrate particles have a surface area of 400 m2/g or less.
12. A fire suppression apparatus comprising:
a container; and
a fire retardant material within the container, the fire retardant material including a powdered material having a plurality of substrate particles and flame retardant particles dispersed on surfaces of the plurality of substrate particles.
13. The fire suppression apparatus as recited in claim 12, wherein the plurality of substrate particles are mica and the flame retardant particles are monoammonium phosphate.
14. The fire suppression apparatus as recited in claim 13, wherein the mica has an average particle size of up to 15 micrometers.
15. The fire suppression apparatus as recited in claim 12, wherein the plurality of substrate particles is selected from a group consisting of mica, silica, diatomaceous earth, and combinations therein, and the flame retardant particles are monoammonium phosphate.
16. A method of producing a fire retardant composition for use in a fire suppression apparatus, comprising:
depositing flame retardant particles onto surfaces of a plurality of substrate particles of a powdered material.
17. The method as recited in claim 16, further including preparing a solution that includes monoammonium phosphate in a carrier liquid and then mixing the solution with the powdered material to deposit the monoammonium phosphate as the flame retardant particles.
18. The method as recited in claim 17, further including removing the carrier liquid such that the monoammonium phosphate deposits as the flame retardant particles onto surfaces of the plurality of substrate particles.
19. The method as recited in claim 17, including spray drying the mixture to deposit the flame retardant particles.
20. The method as recited in claim 17, wherein the solution includes up to about 50 wt. of the flame retardant particles.
21. The method as recited in claim 16, further including grinding the powdered material.
PCT/US2009/069145 2009-12-22 2009-12-22 Fire retardant composition and fire suppression apparatus WO2011078849A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PCT/US2009/069145 WO2011078849A1 (en) 2009-12-22 2009-12-22 Fire retardant composition and fire suppression apparatus

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US2009/069145 WO2011078849A1 (en) 2009-12-22 2009-12-22 Fire retardant composition and fire suppression apparatus

Publications (1)

Publication Number Publication Date
WO2011078849A1 true WO2011078849A1 (en) 2011-06-30

Family

ID=44196069

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2009/069145 WO2011078849A1 (en) 2009-12-22 2009-12-22 Fire retardant composition and fire suppression apparatus

Country Status (1)

Country Link
WO (1) WO2011078849A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2878344A4 (en) * 2012-07-25 2016-04-27 Yamakawa Michiko Fire-extinguishing agent and fire-extinguishing apparatus

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3673088A (en) * 1969-05-14 1972-06-27 Atomic Energy Authority Uk Fire extinguishing powders comprising a cellulose ether additive
US3985538A (en) * 1974-10-24 1976-10-12 Tennessee Valley Authority Pipe reactor-continuous ammoniator process for production of granular phosphates
US4168175A (en) * 1978-04-26 1979-09-18 Vitrofil Corporation Fire retardant compositions
US4346012A (en) * 1979-05-15 1982-08-24 Dainippon Ink & Chemicals, Inc. Powdery fire-extinguishing agent, and process for its preparation
US5472922A (en) * 1993-10-25 1995-12-05 Mobil Oil Corporation Manufacture of improved catalyst

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3673088A (en) * 1969-05-14 1972-06-27 Atomic Energy Authority Uk Fire extinguishing powders comprising a cellulose ether additive
US3985538A (en) * 1974-10-24 1976-10-12 Tennessee Valley Authority Pipe reactor-continuous ammoniator process for production of granular phosphates
US4168175A (en) * 1978-04-26 1979-09-18 Vitrofil Corporation Fire retardant compositions
US4346012A (en) * 1979-05-15 1982-08-24 Dainippon Ink & Chemicals, Inc. Powdery fire-extinguishing agent, and process for its preparation
US5472922A (en) * 1993-10-25 1995-12-05 Mobil Oil Corporation Manufacture of improved catalyst

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2878344A4 (en) * 2012-07-25 2016-04-27 Yamakawa Michiko Fire-extinguishing agent and fire-extinguishing apparatus
JPWO2014016915A1 (en) * 2012-07-25 2016-07-07 通子 山川 Extinguishing media and extinguishers

Similar Documents

Publication Publication Date Title
US4450184A (en) Hollow sphere ceramic particles for abradable coatings
US10828521B2 (en) Fire extinguishing composition
US10335625B2 (en) Phosphate fire-extinguishing composition
Liu et al. Combination intumescent and kaolin‐filled multilayer nanocoatings that reduce polyurethane flammability
Zheng et al. Co‐microencapsulation of ammonium polyphosphate and aluminum hydroxide in halogen‐free and intumescent flame retarding polypropylene
CN105778694B (en) A kind of expansion type facing fire retardant coating
US20210340384A1 (en) Intumescent polyacrylic acid compositions
CN107841049A (en) A kind of polypropene composition of heat discoloration and its preparation method and application
JP2010229804A (en) In-place foaming method for rigid cellular polyurethane insulating layer, and fire preventive coating agent
WO2011078849A1 (en) Fire retardant composition and fire suppression apparatus
KR102454923B1 (en) Fire extinguishing powder for suppression of metal and metal-ion batteries and manufacturing method thereof
KR101543958B1 (en) Method for manufacturing insulating material with expanded perlite
CN104845465A (en) Safe pollution-free fireproof coating
Smith et al. Bio‐Sourced Intumescent Nanocoating
CN115011147B (en) Composite material and preparation method thereof, non-stick cooker and manufacturing method thereof
CN106871179B (en) Grill and its spraying method and micro-wave oven
CN103696134A (en) Flame-retardant non-woven fabric sound-absorbing cotton and preparation method thereof
CN105484055A (en) Polyurethane dry method intermediate layer, as well as polyurethane synthetic leather and preparation method thereof
CN108815787A (en) A kind of core-shell structure extinguishing chemical and preparation method thereof for metallic sodium fire
CN111217551A (en) Inorganic mineral polymeric fiber crystal halogen-free flame retardant powder
JP2016104837A (en) Aqueous flame retardant treatment liquid and flame retardant wood using the same
KR102342633B1 (en) Eco-friendly non-flammable paint composition for coating heating equipment and method of manufacturing the same
CN104497361A (en) New environmentally-friendly rubber flame retardant
CN108467671A (en) A kind of heat insulating function coating material and preparation method thereof
CN108893032A (en) A kind of steel structural traverse formula and preparation process

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 09852674

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 09852674

Country of ref document: EP

Kind code of ref document: A1