• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The present invention relates to a composite system capable of protecting a substrate from jet fires, comprising a lower layer of active fire protection material and an upper layer of fire protection material. The upper layer forms an open cell matrix when exposed to a jet fire, allowing gas from the lower layer to pass around. The upper layer contains a refractory filler and protects the system during initial exposure to high temperature conditions. The upper layer expands upon exposure to high temperature conditions, but expands less than the lower layer.
    公开号:KR20040018321A
    申请号:KR10-2003-7008479
    申请日:2001-12-21
    公开日:2004-03-03
    发明作者:테일러에드워드더블유.；펠드만루빈；쥬니어 립프제임스에이
    申请人:누-켐 인코포레이티드；
    IPC主号:
    专利说明:

    COMPOSITE THERMAL PROTECTIVE SYSTEM AND METHOD
    [2] Various compositions are known to provide protection against fire and other thermal extremes. Currently, such compositions generally comprise a polymeric binder and form char when exposed to fire or high temperature conditions. Charcoal forming compositions can function by a variety of modalities. Several char forming, fire resistant coatings are described in US Pat. No. 5,591,791 to Deogon. In summary, these coatings are flux type coatings that expand to less than two times their initial thickness when exposed to fire or other thermal extremes, and US Pat. No. 2,680,077 to expand to produce charcoal at least five times the initial thickness of the coating. Intumescent coatings, such as those described in Nielsen et al, US Pat. No. 3,284,216 (Kaplan) or US Pat. No. 4,529,467 (Ward et al), and undergo exothermic phase changes and expand two to five times their initial thickness. Sublimable char forming coatings of the type described in US Pat. No. 3,849,178 (Feldman) to form a continuous pore matrix. Intumescent sublimable coatings represent “active” heat protective coatings. In addition, a coating is sometimes applied to the intermediate structure, which is then applied to the substrate as described in US Pat. No. 4,493,945 (Feldman).
    [3] The time required for a given temperature rise, depending on the predetermined thickness of the composition under certain heat flux, environmental and temperature conditions, is a measure of the efficiency of the composition that provides thermal protection for the underlying substrate.
    [4] Eventually, char is extinguished by oxidizing by physical corrosion and chemical processes such as oxygen in the air and free radicals produced by the coating, or else in the fire environment, and protection is almost reduced. Before the charcoal is completely extinguished, the charcoal layer deteriorates and is left broken, and lacks the force necessary to maintain it, which can be destroyed by blowdown or by simple descent (crushing).
    [5] In addition, various methods and structures have been used or suggested for applying these thermal protective coating materials. The most frequent approach is to apply the material directly to the substrate without additional structures. However, in many applications, reinforcements such as fiber glass fabrics, graphite fabrics or wire meshes are embedded in the coating material to reinforce the material and hinder the crushing or dropping of the substrate under conditions of spark or thermal extremes. Examples of such approaches are described in US Pat. No. 3,022,190 (Feldman), US Pat. No. 3,913,290 (Billing et al), US Pat. No. 3,915,777 (Kaplan) and US Pat. No. 4,069,075 (Billing et al). have. Occasionally, the material is first applied to a reinforcing structure, such as a flexible tape or a flexible wire mesh, and the bonded structure is applied to the substrate. Examples of this approach include U.S. Patent 3,022,190 (Feldman), U.S. Patent 4,018,962 (Pedlow), U.S. Patent 4,064,359 (Peterson et al), U.S. Patent 4,276,332 (Castle) and U.S. Patent 4,292,358 (Fryer). et al). In this last mentioned system, the purpose of the reinforcing structure may be to reinforce the resulting composite and to apply the uncured coating material to the substrate without spraying, troweling or painting directly onto the substrate. have. In any previous method and structure, multilayers are often applied to a substrate to provide additional protection.
    [6] However, currently known materials and methods are not as effective as is reasonable with respect to the length of protection for a given weight of protective material. In particular, efficiency is important because the weight or volume is critically limited in many applications. Moreover, coating materials loaded with flame retardants will severely impair their physical properties, otherwise they will limit their suitability as a coating, for example by limiting their film forming characteristics or their water resistance properties.
    [7] Under some extreme fire conditions, all of these known systems require excessive thickness and weight to provide adequate protection. One of the environments in which such extreme fire conditions can occur is near the delivery pipes that transport flammable compressed gases or liquids, typically hydrocarbons from one location to another. Bursts in pipes or breakage of valves or joints can result in high temperatures, high heat fluxes, high speed flames (commonly referred to as "jet fires"). If the pressure difference through rupture or opening is greater than 2: 1, a choked flow condition is produced in the hole and a supersonic flow of gas is created downstream of the hole. The heat flux of this high velocity gas belongs to 300 to 320 KW per m 2, and the temperature is typically from 1,000 ° C. to 1500 ° C. There have been standards that define test procedures for defining jet fires and analyzing the effectiveness of protective coating systems. An important standard is identified as OTI 95 634 "Jet Fire Resistance Test Of Passive Fire Protection Materials" (Health and Safety Executive (UK), Offshore Technology Report, 1996). This document is incorporated herein by reference.
    [8] When exposed to temperature, thermal flux and aerodynamic shear forces of jet fires, currently known coating systems are corroded, quickly extinguished, crushed and applied. Flux coatings tend to produce high density char with good physical and chemical resistance, but in standard jet fire tests, they have been found to allow the underlying substrate to reach critical temperatures in a very short time. In the case of active coatings that expand when exposed to thermal extremes, degradation is usually present in the form of cracks formed in the char as a result of differential thermal stresses created by high thermal gradients and rapid corrosion caused by shear forces.
    [9] In order to increase the strength of the charcoal layer during exposure to thermal extremes, and to limit crushing and cracking, the fabric has been intestinally incorporated into the coating material. As described in US Pat. No. 5,622,774 to Feldman et al, fiberglass fabrics are inexpensive, easy to install, and provide reinforcement in many high temperature applications. However, a jet fire raises the fabric to a temperature above the softening point of the glass (around 870 ° C.), so that the fiber glass fabric collapses. Thus, different fabrics are needed. As previously taught in US Pat. No. 5,622,774 (Feldman et al), and US Pat. No. 5,580,648 (Castle et al), US Pat. No. 5,433,991 (Boyd et al) and US Pat. No. 5,401,793 (Kobayashi et al). The same graphite deposition is one choice. Graphite deposits can generally be pure carbon or precursor materials, as is well known in the art. Also refractory materials, such as quartz (Refrasil) fabrics are used. Metal mesh is inexpensive and widely used, but heavy and difficult to install. However, when reinforced with fiber or mesh, known protection systems are not very effective in protecting against jet fires, requiring a thick and heavy coating to provide limited protection.
    [10] All patents mentioned in this specification are incorporated herein by reference.
    [11] Summary of the Invention
    [12] One of the objectives of one embodiment of the present invention is to provide a thermal protection system which is more effective in protection against jet fires than currently known systems.
    [13] Other objects will be apparent to those skilled in the art from the following.
    [14] According to one aspect of the present invention, there is generally provided a composite system capable of protecting a substrate from a jet fire, the composite system comprising a lower layer of active fire protection material and an upper layer of flux fire protection material; The flux material forms an open cell matrix when exposed to a jet fire, allowing gas from the lower layer to pass around.
    [15] According to another aspect of the invention, generally, a lower layer of active fire protection material that expands when exposed to fire or other high temperature conditions and an upper layer of active fire protection material that expands when exposed to fire or other high temperature conditions. Wherein the upper layer is less expandable than the lower layer, and the upper layer includes a refractory filler that constitutes at least about 7% by weight of the upper layer.
    [16] According to another aspect of the present invention, there is provided a method of applying a layer of a first active thermal protection composition to a substrate, followed by a second step of applying a top layer of a second active thermal protection composition onto the first layer. Wherein the second composition comprises a refractory filler that constitutes at least about 7% by weight of the second composition. Both the first composition and the second composition preferably comprise a polymeric binder and a gas former, and the second composition preferably comprises less gas former (by weight) than the first composition.
    [17] In some embodiments, hot mesh or fabric reinforcement is embedded in the composite system. The reinforcement can be a variety of materials. In one embodiment it is graphite. In another embodiment, it is a metal, such as galvanized steel. In another embodiment, various glass fibers; High temperature polymers such as polyimides, polybenzoimidazoles or polyamides (eg Kevlar); Ceramics such as silica or zirconia; silicon; Or a combination of these materials. Other mesh or fabric reinforcements may also be used, which may be free floating in the composite or pinned to the underlying substrate. In some embodiments, the mesh or fabric is applied to the lower layer before or after the lower layer is substantially cured. When the lower layer is substantially cured, the adhesive layer may be attached to the lower layer, preferably in the form of a thin uncoated upper layer, and the mesh or fabric is embedded in the adhesive layer. In another embodiment, the mesh or fabric is embedded in the top layer. In another embodiment, the mesh or fabric is embedded in the underlying layer. In other embodiments, especially when the mesh is pinned to the substrate and the thickness of the system is small, the mesh can extend through both layers of the system. In another embodiment, the amount and size of the fibers in the form of pieces in the upper layer is selected to replace the mesh or fabric. In other embodiments, no mesh or fabric reinforcement is needed due to the requirements of the system. In other embodiments, meshes or fabrics are used to make the system stand out from the substrate as in US Pat. No. 4,493,945 (Feldman).
    [18] In a preferred embodiment of the composite system, the underlayer is applied directly to the substrate and adhered to the substrate. In order to assist the adhesion, it is generally understood that the primer is first applied to the substrate in accordance with generally accepted conventions.
    [19] In a preferred embodiment, the thickness of the underlayer is about 1 to 25 mm. In one embodiment, the thickness of the underlayer is less than 15 mm. In another embodiment, the thickness of the underlayer is from about 3 mm to about 10 mm.
    [20] The lower layer expands to more than twice its original thickness to cope with high heat conditions. In some embodiments, the underlayer expands from about 2 times to about 5 times the thickness when applied. In another embodiment, the underlayer expands 5 to 100 times its original thickness. The lower layer preferably comprises about 30% to about 65% polymer resin and at least 30% blowing agent (gas former). Various formulations which can be used are known in the art, for example some of which are disclosed in the patents mentioned above. Others are disclosed in US Pat. No. 5,487,946 to McGinniss et al. Others are commercially available, for example Chartek 7 (Akzo Novel / International Paint, Ltd.), Albi Clad800 (Albi Manufacturing division of Stanchem. Inc.) or Thermo-Lag 3000, Thermo-Lag 2000, Thermo-Lag 440, Thermo-Lag 330 or Thermo-Lag 220 (Nu-Chem, Inc.).
    [21] In a preferred embodiment, the thickness of the upper layer is about 1 to 25 mm. In one embodiment, the thickness of the upper layer is less than 15 mm. In another embodiment, the thickness of the top layer is between about 2 mm and about 6 mm. If a mesh or fabric reinforcement is used, the thickness of the upper layer is preferably about 2.5 mm or more.
    [22] The upper layer composition forms part of the present invention as a combination with the lower layer and by itself. That is, according to another aspect of the present invention, there is provided a thermal protective composition comprising a polymeric binder, 5% to 30% blowing agent that turns a solid into a gas at high temperatures to which the composition can be exposed, and at least 7% refractory filler do.
    [23] The refractory filler preferably comprises particles or fibers, or both. The filler preferably comprises glass, graphite, or ceramic fibers and particles (granules). The glass can be in various forms. Ceramics include, for example, metal oxides such as silica, alumina, mullite, magnesium oxide, titanium dioxide and zirconia; Metal carbides such as silicon carbide, aluminum carbide, boron carbide and zirconium carbide; Metal nitrides such as silicon nitride, boron nitride and aluminum nitride; Metal silicates such as aluminum silicate, cordierite, zircon and steatite; And metal borides such as silicon tetraboride, tungsten boride and zirconium boride. Graphite may be in the form of substantially pure carbon or may be a precursor material that is converted to substantially pure carbon in a fire state. Any fiber should be limited to less than about 7 mm in length for use in existing spray applicators, but if the top layer is applied by other methods such as trowelling, brushing, rolling, forming, Longer fibers can also be used. In one embodiment, the filler comprises at least about 15% by weight of the composition. In other embodiments, they comprise about 20% to about 30% by weight of the composition. In other embodiments, they comprise at least 25% by weight of the composition. Inert fillers increase the corrosion resistance of the system and significantly increase its efficacy. The inert filler is preferably selected to re-radiate (such as by reflection) heat from a high temperature fire more effectively than the top layer containing no filler.
    [24] A small amount of gaseous composition is introduced into the upper layer to ensure the formation of an open porous matrix in the fire state. In one embodiment, the gas former comprises less than 30% by weight of the top layer composition. In another embodiment, the gas former comprises about 10% to about 25% by weight of the top layer composition. The top layer composition is formulated to swell less than the bottom layer, preferably to about 10% to 100% of its initial thickness in a fire state. The upper layer inhibits the expansion of the lower layer but does not interfere with the expansion of the lower layer.
    [25] In presently preferred embodiments, the top layer is modified with a softening agent to increase flexibility and elasticity. In the presently most preferred embodiment, the top layer comprises about 35% to about 65% epoxy resin. In order to increase its flexibility and elasticity, it is preferable to modify the resin, for example using polysulfide. Preference is given to curing with amines. Other resins such as polyamides, polyimides, acrylics, urethanes, polyisocyanurates and the like can also be used. The polysulfide and amine curable components of the presently preferred resins can impart sufficient flexibility to the upper layer to form an open porous matrix that is gas permeable upon heating and can also expand the lower layer, especially the lower layer of the highest heating site. Only a portion of the gas from the lower layer will penetrate through the upper layer. The other part will induce limited expansion of the lower layer. The upper layer is also resistant to high temperature stresses caused by the temperature of the layer surface being significantly higher and the temperature below it much lower.
    [26] Alternatively, additives may be added to the upper layer to improve the properties of the upper layer. For example, boron or zinc can be added in elemental or combined form. Coloring agents, radiation regulating agents, rheology modifiers, plasticizers and the like can also be added.
    [27] The upper layer also provides an advantage to the system when not exposed to excessive heat or fire. It makes the system more resistant to environmental conditions such as water, salt, radiation and corrosion, and also more resistant to physical abrasion. One embodiment of the present invention successfully tested both with and without top coat using the deposition / freeze / dry cycle test program described in the NORSOK M-501 standard (revised Dec. 4, 1999). A 60-minute hydrocarbon fire endurance test (Norway Petroleum Bureau Standard NS 3904) was performed on the tested (non-scribed) and uncirculated test programs. This standard is incorporated herein by reference.
    [28] Unlike traditional top coats, the upper layer of the present invention has a substantial thickness of at least 1 mm, preferably at least 2 mm, and is compatible with the composition of the underlying layer. In a preferred embodiment of the present invention, the upper and lower layers comprise similar resin systems, but differ in the amount of gas forming material and the amount of refractory filler in them.
    [29] While the present invention is not desirable in many applications where it is applied, in some applications, such as for protective pipes that do not require long-term durable protection from fire or other high temperature conditions, the upper layer can be used without a lower layer.
    [30] The composites of the present invention, in the standard jet fire test procedure, provide 30% or more longer term protection than the protection provided by a system comprising only the top or bottom composition, even when applied to the full thickness of the composite system. Confirmed. Preferred systems of the present invention provide at least 50% longer term protection, sometimes longer than 100%.
    [31] Various systems can be protected using the system of the present invention. In particular, it is useful for protecting hydrocarbon recovery or treatment facilities, for example steel structures of deep sea drilling platforms and petroleum treatment plants. In addition, the systems of the present invention can be used to protect the leading edges of other substrates, such as other metals, plastics, pipes, flanges, pins, bulkheads, tanks, rocket launchers, and supersonic aircraft.
    [32] Other aspects of the invention will be better understood from the following description.
    [33] Best Mode for Carrying Out the Invention
    [34] The invention is illustrated below by way of non-limiting examples. Those skilled in the art will be able to practice and use the present invention through the description of the examples, and the described examples include several embodiments, applications, modifications, alternatives, etc., in addition to what are presently considered to be the best embodiments for practicing the present invention. It is.
    [1] The present invention relates to a heat protective coating. In particular, it is useful for protecting the substrate from very high strength, high speed and high temperature conditions by applying it to a coating applied to the substrate.
    [35] Example 1
    [36] Compositions for use as removable top layers include 35% to 65% by weight of flexible polymer resins (such as modified epoxy resins, in particular epoxy polysulfide resins), gas formers (polyol spumifices) ), Amine blowing agents and phosphate acid formers). 5% to 30% by weight and about 10% to about 40% fire resistant filler. The composition exemplified above is a two component modified epoxy having the following nominal composition:
    [37] weight% Melamine5 Ammonium polyphosphate10 Pentaerythritol5 Epoxy Resin (Bisphenol A)25 Polysulfide and Amine Curing Agent25 Fiberglass (chopped)5 Ceramic particles25
    [38] Example 2
    [39] Lower layer active thermal protective compositions may comprise from 30% to 70% by weight of polymer resins (such as modified epoxy resins, in particular epoxy polysulfide resins) and gas formers (polyol spumifixes, amine blowing agents and phosphate acid formers). For example) to 20 to 50% by weight. The composition for use in the following tests is an epoxy-based thermally activated two-component coating, which volatilizes at a fixed temperature when exposed to sparks or thermal extremes, and slightly increases in volume through the formation of an open cell matrix (2 of initial thickness). More than twice) and absorbs and blocks heat to protect the substrate. The composition is composed of bis- (ethylene oxy) methane containing a multifunctional alcohol, 1,3,5-triazine-2,4,6-triamine, an epoxy resin and a disulfide bond and a curable terminal thiol group (polysulfide) Polymers.
    [40] The composition exemplified above is a modified two component epoxy having the following nominal composition:
    [41] weight% Melamine5 Ammonium polyphosphate25 Pentaerythritol10 Epoxy resin30 Polysulfide20 glass fiber5 catalyst5
    [42] In general, test articles as described in OTI 95634 (1996) were sprayed 3 mm thick using the underlayer composition.
    [43] The graphite fabric was pressed into the lower layer prior to curing. The lower layer was cured for 17 hours and the upper layer composition of Example 1 was sprayed to the lower layer at 3 mm. The composite was cured at 30 ° C. for 1 month.
    [44] Example 3
    [45] Test articles prepared according to Example 2 were exposed to jet fire following the procedure described in OTI 95634 (1996). As a result of the test, the composite structure was protected for about 60 minutes under test conditions.
    [46] Smaller test results showed that the composite system provided a much longer protective effect than the protection provided by only the upper or lower layers of thickness equal to the total thickness of the composite. The test results are summarized in Table 3 below.
    [47] Small scale jet fire simulation Temperature approximately 1100 degrees Celsius Heat flux about 300 KW / m 2Coating Composition A = Bottom Coating, B = Top Coating Test article coating composition time to 400 ℃ Flat plate 6 "x6" x1 / 4 "A 3 mm and B 3 mm 44 minutes 6 "x6" x1 / 4 "A 3 mm 27 min pipe 4 "B 5 mm diameter 10 minutes 4 "diameter A 3 mm and B 3 mm 26 minutes (Wall thickness: 3/8 ")
    [48] Example 4
    [49] Full range testing of the composite system according to the invention was carried out in accordance with OffShow Technology Report OTI 95 634. The upper and lower compositions were formed as shown in Example 1 (Table 1) and Example 2 (Table 2). Test pieces were primed with epoxy primer and coated with a nominal 3 mm top layer composition and a nominal 3 mm top layer composition reinforced with a sized carbon fiber fabric having about 2.3 openings per cm 2 . The fabric weight was about 105 g per 1 m 2 and the tie layers of the fabric were overlapped. The total thickness of the composite system was 6 mm, with individual measurements ranging from 5 mm to 7 mm.
    [50] At the end of 30 minutes, the average box temperature rose 250 ° C. above ambient and the average web temperature rose to 239 ° C. After 75 minutes, the average box temperature rose 327 ° C above ambient and the average web temperature rose to 382 ° C. The maximum rises at 30 minutes were 428 ° C and 265 ° C, respectively, and at 75 minutes the maximum rises were 450 ° C and 411 ° C, respectively.
    [51] In addition, tests were performed according to the Osher Technology Report OTI 95 634 for systems comprising only the top layer composition (Example 1, Table 1). The test piece was primed with an epoxy primer and the top layer composition coated with a nominal thickness of 12 mm on the back side of the box and 16 mm on the web. The entire structure was reinforced with a carbon fiber woven sized about 8 mm from the box and web surface. Additional fabric layers were used at nominal 12 mm from the web surface only on the web. The fabric had about 2.3 openings per cm 2 , weighed about 105 g per m 2 , and the tie layers of the fabric overlapped. The measured average thickness of the system was 12.7 mm (10.5-16 mm) on the back of the box and 15.2 mm (13-17 mm) on the web of test specimens.
    [52] At the end of 30 minutes, the average box temperature rose 121 ° C. above ambient and the average web temperature rose to 175 ° C. After 70 minutes, the average box temperature rose 180 ° C. above ambient and the average web temperature rose to 347 ° C. After 120 minutes, the average box temperature rose 207 ° C above ambient and the average web temperature rose to 474 ° C. The maximum rises were 140 ° C. and 225 ° C. at 30 minutes, the maximum rises were 210 ° C. and 462 ° C. at 70 minutes, and 239 ° C. and 628 ° C. at 120 minutes, respectively. After 120 minutes, all the fabrics were intact and the metal substrate was not exposed to a jet fire.
    [53] In addition, the tests were performed according to the Osher Technology Report OTI 95 634 for two systems comprising only the bottom layer composition (Example 2, Table 2). The test piece was primed with an epoxy primer and coated with a lower layer composition (test A) having a nominal thickness of 5 mm and a lower layer composition with a nominal thickness of 11 mm (test B). In each test, the entire structure was reinforced with a 19-gauge wire mesh with a 12.7 x 12.7 mm opening pinned to the substrate. In test A, the measured average thickness of the system was 4 mm (2.5-5 mm) on the back side of the box and 4.7 mm (3-7 mm) on the web of the test piece. In test B, the measured average thickness of the system was 11 mm (9-14 mm) on the back of the box and 11.4 mm (9-13 mm) on the web of the test piece.
    [54] At the end of 30 minutes, the average box temperature of test A rose 352 ° C above ambient and the average web temperature rose to 473 ° C.
    [55] At the end of 30 minutes, the average box temperature of Test B rose 200 ° C. above ambient and the average web temperature rose to 180 ° C. After 74 minutes, the average box temperature rose 318 ° C above ambient and the average web temperature rose to 325 ° C. Maximum rises at 74 minutes were 604 ° C and 376 ° C. Metal mesh and metal substrates were exposed by jet fire.
    [56] Through the above description, it can be seen that several objects and advantages of the present invention are realized, and other beneficial results can be obtained.
    [57] Since various modifications may be made to the above constructions without departing from the scope of the present invention, it is understood that all technical contents of the present application including the drawings are intended to be interpreted as non-limiting examples.
    权利要求:
    Claims (44)
    [1" claim-type="Currently amended] A composite system that protects a substrate from fire or other high temperature conditions, the system comprising a lower layer of active fire protection material and an upper layer of flux fire protection material, wherein the flux material is an open cell matrix when exposed to high temperature conditions. And form gas to allow gas from the lower layer to pass through.
    [2" claim-type="Currently amended] The system of claim 1, wherein the top layer comprises at least about 7% by weight of inert filler.
    [3" claim-type="Currently amended] The system of claim 1, wherein the top layer comprises at least 15% by weight of inert filler.
    [4" claim-type="Currently amended] The system of claim 1, wherein the top layer comprises at least 20% by weight of inert filler.
    [5" claim-type="Currently amended] The system of claim 2, wherein the inert filler is selected from the group comprising glass, graphite, and ceramics.
    [6" claim-type="Currently amended] The system of claim 2, wherein the inert filler increases reradiation of heat by the top layer.
    [7" claim-type="Currently amended] The system of claim 1, wherein the system is capable of protecting against jet fire for at least 30% more time than protection provided by coatings of the same thickness on the upper or lower layers.
    [8" claim-type="Currently amended] The system of claim 1, further comprising a mesh or fabric reinforcement embedded in the system.
    [9" claim-type="Currently amended] The system of claim 1, wherein the underlayer is about 1 to about 25 mm in thickness.
    [10" claim-type="Currently amended] The system of claim 1, wherein the underlayer is about 2 to about 15 mm in thickness.
    [11" claim-type="Currently amended] The system of claim 10, wherein the top layer is about 2 to about 6 mm thick.
    [12" claim-type="Currently amended] The system of claim 1, wherein the top layer is about 1 to about 25 mm thick.
    [13" claim-type="Currently amended] The system of claim 1, wherein the top layer is about 1 to about 6 mm thick.
    [14" claim-type="Currently amended] A composite system capable of protecting a substrate from jet fires, the system comprising a lower layer of active fire protection material that expands when exposed to fire or other high temperature conditions, and an active fire that expands when exposed to fire or other high temperature conditions. A top layer of protective material, the top layer less expanding than the bottom layer, wherein the top layer comprises a filler of a refractory material that constitutes at least about 7% by weight of the top layer.
    [15" claim-type="Currently amended] The system of claim 14, wherein the top layer comprises at least 15% by weight of the refractory material.
    [16" claim-type="Currently amended] The system of claim 14, wherein the inert filler is selected from the group comprising glass, graphite, and ceramics.
    [17" claim-type="Currently amended] 15. The system of claim 14, wherein the system is capable of protecting against jet fire for at least 30% more time than protection provided by coatings of the same thickness on the upper or lower layers.
    [18" claim-type="Currently amended] The system of claim 14, further comprising a mesh or fabric reinforcement embedded within the system.
    [19" claim-type="Currently amended] The system of claim 14, wherein the underlayer is about 1 to about 25 mm in thickness.
    [20" claim-type="Currently amended] The system of claim 14, wherein the underlayer is about 2 to about 6 mm in thickness.
    [21" claim-type="Currently amended] The system of claim 20, wherein the top layer is about 2 to about 6 mm in thickness.
    [22" claim-type="Currently amended] The system of claim 14, wherein the top layer is about 1 to about 25 mm thick.
    [23" claim-type="Currently amended] The system of claim 1, wherein the top layer is about 1 to about 6 mm thick.
    [24" claim-type="Currently amended] A first step of applying a layer of a first active thermal protection composition to the substrate, and then a second step of applying a top layer of a second active thermal protection composition to the first layer, wherein the second composition comprises: 2 A method of protecting a substrate from high heat conditions, comprising a filler of a refractory material that constitutes at least about 7% by weight of the composition.
    [25" claim-type="Currently amended] The composite system of claim 24, wherein the first composition and the second composition comprise a polymeric binder and a gas former, wherein the second composition comprises less gas former than the first composition, wherein the method is applied to a substrate. To provide.
    [26" claim-type="Currently amended] 27. The method of claim 25, further comprising embedding a hot mesh or fiber reinforcement in the composite system.
    [27" claim-type="Currently amended] The method of claim 26, wherein the reinforcement comprises a graphite fabric.
    [28" claim-type="Currently amended] 27. The method of claim 26, wherein the reinforcement comprises a metal mesh.
    [29" claim-type="Currently amended] The method of claim 24, wherein the underlayer is applied at a curing thickness of about 1 to about 25 mm.
    [30" claim-type="Currently amended] The method of claim 29, wherein the underlayer is less than 15 mm in thickness.
    [31" claim-type="Currently amended] The method of claim 24, wherein the underlayer responds to high thermal conditions by expanding to at least twice the initial thickness.
    [32" claim-type="Currently amended] The method of claim 24, wherein the top layer is applied at a curing thickness of about 1 to about 15 mm.
    [33" claim-type="Currently amended] The method of claim 32, wherein the top layer is less than about 6 mm in thickness.
    [34" claim-type="Currently amended] The method of claim 24, wherein the top layer responds to high thermal conditions by expanding to an average thickness of less than twice the initial thickness.
    [35" claim-type="Currently amended] A thermal protective composition comprising a polymeric binder, from 5% to 30% of a blowing agent and from at least 7% of a refractory filler, which changes from solid to gas at the high temperatures encountered by the composition.
    [36" claim-type="Currently amended] 36. The composition of claim 35, wherein the refractory filler comprises both particles and fabrics.
    [37" claim-type="Currently amended] 36. The composition of claim 35, wherein the filler comprises ceramic particles and glass fibers.
    [38" claim-type="Currently amended] 36. The composition of claim 35, wherein the filler comprises at least one material selected from the group consisting of glass, graphite, and ceramics.
    [39" claim-type="Currently amended] The composition of claim 35, wherein the filler comprises at least about 15% by weight of the composition.
    [40" claim-type="Currently amended] The composition of claim 35, wherein the filler comprises about 20% to 30% by weight of the composition.
    [41" claim-type="Currently amended] 36. The composition of claim 35, wherein the blowing agent comprises 10% to 30% by weight of the composition.
    [42" claim-type="Currently amended] 36. The composition of claim 35, comprising a flexible agent.
    [43" claim-type="Currently amended] 36. The composition of claim 35, wherein the composition comprises about 35% to about 65% modified epoxy resin.
    [44" claim-type="Currently amended] The composition of claim 43 wherein the epoxy resin is modified with polysulfide and cured with amine.
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    同族专利:
    公开号 | 公开日
    CN1487981A|2004-04-07|
    US20020119717A1|2002-08-29|
    WO2002055615A9|2003-11-13|
    RU2003121310A|2005-02-27|
    NO20032819L|2003-08-18|
    CN1276956C|2006-09-27|
    US6855401B2|2005-02-15|
    EP1345998A2|2003-09-24|
    RU2303617C2|2007-07-27|
    WO2002055615A3|2003-05-01|
    WO2002055615A2|2002-07-18|
    US20050171242A1|2005-08-04|
    NO20032819D0|2003-06-19|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    2000-12-22|Priority to US25813800P
    2000-12-22|Priority to US60/258,138
    2001-12-21|Application filed by 누-켐 인코포레이티드
    2001-12-21|Priority to PCT/US2001/049912
    2004-03-03|Publication of KR20040018321A
    优先权:
    申请号 | 申请日 | 专利标题
    US25813800P| true| 2000-12-22|2000-12-22|
    US60/258,138|2000-12-22|
    PCT/US2001/049912|WO2002055615A2|2000-12-22|2001-12-21|Composite thermal protective system and method|
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