Patent Grant
8329819
1. Field of the Invention
The invention relates to organic/inorganic composites showing excellent fire resistant performance and a fire-resistant plate containing the organic/inorganic composite.
2. Description of the Related Art
Fire resistant or fire retardant materials can be used as architectural or decorative materials. Architecture materials disclosed in Taiwan Patent Nos. 583,078 and 397,885 primarily comprise a stacked layer, serving as a fire resistant layer of nonflammable inorganic materials such as pearlite (or perlite), MgCl2, MgO, CaCO3 or cement. In addition, a stiff fire resistant laminate can be obtained from flexible substrates of fibers or nonwovens blended with flame retardants, foaming agents and 50˜80 inorganic materials by weight.
Fire resistant coatings, serving as decorative materials, disclosed in Taiwan Patent Nos. 442,549, 499,469 and 419,514 comprise a combination of foaming and intumescent agents, carbonization agents, flame retardants, and adhesives which foam and intumesce when exposed to fire. U.S. Pat. No. 5,723,515 discloses a fire-retardant coating material comprising a fluid intumescent base material having a foaming agent, a blowing agent, a charring agent, a binding agent, a solvent, and a pigment, increasing resistance to cracking and shrinking. A compound disclosed in U.S. Pat. No. 5,218,027 is manufactured from a composition of a copolymer or terpolymer, a low modulus polymer, and a synthetic hydrocarbon elastomer. The fire retardant additive comprises a group I, group II or group III metal hydroxide with the proviso that at least 1% by weight of the composition is in the form of an organopolysiloxane. U.S. Pat. No. 6,262,161 relates to filled interpolymer compositions of ethylene and/or alpha-olefin/vinyl or vinylidene monomers, showing improved performance under exposure to flame or ignition sources, and articles fabricated therefrom. The articles can be in the form of a film, sheet, multilayered structure, floor, wall, or ceiling covering, foams, fibers, electrical devices, or wire and cable assemblies. Conventional flame retardant polymer compositions are obtained by physical bending of organic polymer and inorganic flame retardant, wherein coupling agents or surfactants are typically incorporated to improve the dispersity of inorganic flame retardant. However, because the organic polymer does not react with inorganic component to form a well-structured composite by the formation of chemical bonds, the conventional flame retardant compositions easily melt, ignite, or produce flaming drops under exposure to flame or ignition sources.
Specifically, as shown in
In view of the problems in conventional technology, the invention utilizes a fire resistant composite material comprising various inorganic particles fully dispersed in a polymer, copolymer, or oligomer having reactive functional groups. The inorganic particles also contain reactive functional groups, originally or after surface modification, that can react with the corresponding reactive functional groups of the organic component to form organic/inorganic composite materials. Through the reaction between organic and inorganic components, the mechanical and fire resistant properties of the organic polymer are strengthened and enhanced. As a well-structured composite is provided by the formation of chemical bonds, the char layer formed on the surface is firm and can maintain its structural integrity without peeling or cracking, effectively preventing direct heat transfer to the interior.
The organic/inorganic composite of the invention comprises a polymer, copolymer, or oligomer having a first reactive functional group; and inorganic particles having a second reactive functional group; wherein the inorganic particles are chemically bonded to the polymer, copolymer, or oligomer via a reaction between the first and second reactive functional groups.
The invention further provides a fire-resistant plate comprising the disclosed composite.
A detailed description is given in the following embodiments with reference to the accompanying drawings.
The invention can be more fully understood by reading the subsequent detailed description and examples with references made to the accompanying drawings, wherein:
a-1d show conventional intumescent fire resistant materials subjected to a flame test;
The following description is of the best-contemplated mode of carrying out the invention. This description is made for the purpose of illustrating the general principles of the invention and should not be taken in a limiting sense. The scope of the invention is best determined by reference to the appended claims.
When the organic/inorganic composite material is burned or exposed to fire, the organic component forms a char layer and the inorganic particles radiate absorbed heat. The inorganic particles also strengthen the mechanical properties of the structure through the reaction between inorganic and organic materials, so that char layer formed on the surface is firm and can maintain its structural integrity without peeling or cracking, effectively preventing direct heat transfer to the interior. The fire resistant material is not only flame retardant but also protective of interior materials. As a result, the duration of fire resistant ability is tremendously improved.
In the invention, inorganic particles having reactive functional groups, originally or after surface modification, are well dispersed in and reacted with an organic component such as polymer, monomer, oligomer, prepolymer, or copolymer to enhance the fire resistant and mechanical properties. In general, the organic/inorganic composite may comprise 10-90% by weight of the organic component, and 90-10% by weight of the inorganic particle. Preferably, the organic/inorganic composite comprises 30-70% by weight of the organic component, and 70-30% by weight of the inorganic particle, and more preferably 40-60% by weight of the organic component, and 60-40% by weight of the inorganic particle.
The organic component in the resulting composite may comprise polymer, copolymer or oligomer. For the purposes of the invention, the term “polymer” or “copolymer” refers to compounds having number average molecular weights in the range from 1500 to over 1,00,000 Daltons, while “oligomer” refers to compounds having number average molecular weights in the range of from 200 to 1499 Daltons.
In the organic/inorganic composite, the organic component and the inorganic particles are chemically bonded via reactions of corresponding reactive functional groups. The reactive functional groups of the organic component and inorganic particles include, but are not limited to, —OH, —COOH, —NCO, —NH3, —NH2, —NH, and epoxy groups. For example, an organic component having —COOH or —NCO groups (e.g., organic acid or reactive polyurethane) can be employed to react with inorganic particles having —OH groups (e.g., metal hydroxide). In addition, an organic component having epoxy groups can be employed to react with inorganic particles having —NH2 groups. Alternatively, an organic component having —OH groups (e.g., polyvinyl alcohol) may react with inorganic particles having —COOH or —NCO groups, and an organic component having —NH2 groups may react with inorganic particles having epoxy groups.
Organic components suitable for use herein include any monomer, oligomer, monopolymer, copolymer, or prepolymer that contains the above-mentioned reactive functional groups. The reactive functional groups may reside in backbone or side chain of the polymer. Preferred organic components include polyoragnic acid, polyurethane, epoxy, polyolefin, and polyamine. The polyorganic acid includes momopolymers or copolymers that contain carboxylic or sulfonic acids such as poly(ethylene-co-acrylic acid and poly(acrylic acid-co-maleic acid). Illustrative examples of epoxy include bis(3,4-epoxy-6-methylcyclohexylmethyl) adipate, vinylcyclohexene dioxide, diglycidyl tetrahydrophthalate, diglycidyl hexahydrophthalate, bis(2,3-epoxycyclopentyl) ether resin, glycidyl ethers of polyphenol epoxy resin. Polyamines suitable for use include polyamine and polyimide. Illustrative examples of polyamine include nylon 6 ((NH(CH2)5CO)n), nylon 66 ((NH(CH2)6—NH—CO(CH2)4CO)n), and nylon 12 ((NH(CH2)11CO)n). The polyimide includes diamine such as 4,4-oxydianiline, 1,4-bis(4-aminophenoxy)benzene, or 2,2-bis[4-(4-aminophenoxy)phenyl]propane; and also includes polyimide synthesized by the diamine and dianhydride such as oxydiphthalic anhydride, pyromellitic dianhydride, or benzophenone tetracarboxylic dianhydride. Polyolefins suitable for use include copolymers of an olefin monomer and a monomer having the above reactive functional groups. It should be noted that the organic component also includes monomer, oligomer, copolymer and prepolymer of the above illustrative polymers. In addition, the organic components may be used alone or in admixture of two or more.
Inorganic particles suitable for use herein are those having corresponding functional groups, originally or after surface modification, that can react with the functional groups of the organic component. Preferred inorganic particles include hydroxide, nitride, oxide, carbide, metal salt, and inorganic layered material. Hydroxides include metal hydroxide such as Al(OH)3 or Mg(OH)2. Nitrides include, for example, BN and Si3N4. Carbides include, for example, SiC. Metal salts include, for example, CaCO3. Inorganic layered materials include, for example, clay, talc, and layered double hydroxide (LDH), wherein the clay can be smectite clay, vermiculite, halloysite, sericite, saponite, montmorillonite, beidellite, nontronite, mica, or hectorite. The inorganic particles can also be used in admixture of two or more. For example, a clay having reactive functional groups can be used in combination with metal hydroxide. Suitable inorganic particles include micro-sized particles and nano-sized particles. Nano-sized particles having diameters between 1 and 100 nm are particularly preferred because the smaller particle size the greater the surface area per unit weight.
The organic component and the inorganic particles can be directly mixed for reaction to form covalent bonds or ionic bonds, or the reaction can be carried out in various solvates (e.g., water, ethanol, or methyl ethyl ketone). The reaction temperature is generally from room temperature to about 150° C. and the reaction time may vary from 10 minutes to few days, depending on the starting materials used.
The organic/inorganic composite of the invention can be molded into fire-resistant plates, flakes, or films by various methods. Note that while the term “fire-resistant plate” is used throughout the specification for the sake of simplicity, it will be understood to include films having a thickness of less than 0.5 mm, flakes having a thickness between 0.5 and 2 mm, or plates having a thickness exceeding 2 mm. Suitable molding methods include conventional compression molding, injection molding, extrusion molding, calender molding, and the like. The sample can be oven-dried or kept at room temperature until molding.
The fire-resistant plate of the invention can be mounted onto the surfaces of flammable or inflammable articles by adhesives or mechanical tools (e.g., screws, nails, or clamps) to improve the fire resistance. Furthermore, the fire-resistant plate can be fabricated into a multilayer structure with or without other flammable or inflammable plates. When the organic/inorganic composite of the invention is burned or exposed to fire, the polymer forms a char layer and the inorganic particles radiate absorbed heat. The inorganic particles also strengthen the mechanical properties of the structure through the reaction between inorganic and organic materials, so that the formed char layer is firm and can maintain its structural integrity without peeling or cracking, effectively preventing direct heat transfer to the interior. The fire-resistant plate is not only flame retardant but also protective of interior materials. As a result, fire resistance is extended significantly. In preferred embodiments, the fire-resistant plate is capable of withstanding flame temperatures between 1000 and 1200° C. for more than 3 minutes. Because the organic component and the inorganic particles are chemically bonded (compared to the conventional physical bending products), the fire-resistant composite of the invention does not melt, ignite or produce flaming drops under exposure to flame or ignition sources.
The fire-resistant plate of the invention has a wide range of application. For example, it is suitable in fire-resistant spacer plates, or fire-resistant wallpaper. Further, it can be fabricated into flexible fire-resistant plates. Accordingly, those of ordinary skill in the art may incorporate various additives depending on the specific application. For example, flame retardant such as melamine phosphates, red phosphorus, and phosphorus-based flame retardant may be present to improve the flame retardancy. Silane (such as TEOS or TEVS) or siloxane may be present to strengthen structural integrity and facilitate curing. Glass sand and glass fiber may be present to improve the heat resistance and strengthen structural integrity. The amount of these additives is typically between 0.1 and 20 parts by weight, based on 100 parts by weight of the organic/inorganic composite.
Poly(ethylene-co-acrylic acid) containing R—COOH was dissolved or dispersed in water. Subsequently, inorganic particles Al(OH)3 with reactive functional groups M-OH were added to the polymer solution, and the mixture was stirred at 70˜90° C. for 20 minutes. 1 mm-thick mixture slurry was coated on a teflon sheet, and then placed in an oven, dried at 60° C. for 60 minutes, 80° C. for 60 minutes, 100° C. for 60 minutes, 120° C. for 30 minutes, 140° C. for 30 minutes, 160° C. for 30 minutes, 180° C. for 30 minutes, and finally, molded at 200° C. for 240 minutes.
As shown in
According to this embodiment, the duration of fire resistance was more than 3 minutes due to the strengthened sample layer, i.e. R—COOH of poly(ethylene-co-acrylic acid) reacted with M-OH of Al(OH)3 to form chemical bonds rather than physical blending.
Poly(ethylene-co-acrylic acid) containing R—COOH was dissolved or dispersed in water. Subsequently, inorganic particles Mg(OH)2 with reactive functional groups M-OH were added to the polymer solution, and the mixture was stirred at 70-90° C. for 20 minutes. 1 mm-thick mixture slurry was coated on a teflon sheet, and then placed in an oven, dried at 60° C. for 60 minutes, 80° C. for 60 minutes, 100° C. for 60 minutes, 120° C. for 30 minutes, 140° C. for 30 minutes, 160° C. for 30 minutes, 180° C. for 30 minutes, and finally, molded at 200° C. for 240 minutes.
As shown in
According to this embodiment, the duration of fire resistance was more than 3 minutes due to the strengthened sample layer, i.e. R—COOH of poly(ethylene-co-acrylic acid) reacted with M-OH of Mg(OH)2 to form chemical bonds rather than physical blending.
Poly(acrylic acid-co-maleic acid) containing R—COOH was dissolved or dispersed in water. Subsequently, inorganic particles Al(OH)3 with reactive functional groups M-OH were added to the polymer solution, and the mixture was stirred at 70-90° C. for 20 minutes. 1 mm-thick mixture slurry was coated on a teflon sheet, and then placed in an oven, dried at 60° C. for 60 minutes, 80° C. for 60 minutes, 100° C. for 60 minutes, 120° C. for 30 minutes, 140° C. for 30 minutes, 160° C. for 30 minutes, 180° C. for 30 minutes, and finally, molded at 200° C. for 240 minutes.
As shown in
According to this embodiment, the duration if fire resistant ability was more than 3 minutes due to the strengthened sample layer, i.e. R—COOH of poly(acrylic acid-co-maleic acid) reacted with M-OH of Al(OH)3 to form chemical bonds rather than physical blending.
Polyurethane containing R—NCO was dissolved or dispersed in hexane. Subsequently, inorganic particles Al(OH)3 with reactive functional groups M-OH were added to the polymer solution, and the mixture was stirred at room temperature for 20 minutes. 1 mm-thick mixture slurry was coated on a teflon sheet, and then placed in an oven, molded at 60° C. for 120 minutes.
As shown in
According to this embodiment, the duration of fire resistance was more than 3 minutes due to the strengthened sample layer, i.e. R—NCO of polyurethane reacted with M-OH of Al(OH)3 to form chemical bonds rather than physical blending.
Poly(ethylene-co-acrylic acid) containing R—COOH was dissolved or dispersed in water. Subsequently, unmodified inorganic particles SiO2 were added to the polymer solution, and the mixture was stirred at 70˜90° C. for 20 minutes. 1 mm-thick mixture slurry was coated on a teflon sheet, and then placed in an oven, dried at 60° C. for 60 minutes, 80° C. for 60 minutes, 100° C. for 60 minutes, 120° C. for 30 minutes, 140° C. for 30 minutes, 160° C. for 30 minutes, 180° C. for 30 minutes, and finally, molded at 200° C. for 240 minutes.
As shown in
According to this comparative example, the duration of fire resistance was less than 2 minutes because R—COOH of poly(ethylene-co-acrylic acid) did not react with unmodified SiO2 to form a well-structured composite by the formation of chemical bonds.
Poly(acrylic acid-co-maleic acid) containing R—COOH was dissolved or dispersed in water. Subsequently, unmodified inorganic particles Al2O3 were added to the polymer solution, and the mixture was stirred at 70˜90° C. for 20 minutes. 1 mm-thick mixture slurry was coated on a teflon sheet, and then placed in an oven, dried at 60° C. for 60 minutes, 80° C. for 60 minutes, 100° C. for 60 minutes, 120° C. for 30 minutes, 140° C. for 30 minutes, 160° C. for 30 minutes, 180° C. for 30 minutes, and finally, molded at 200° C. for 240 minutes.
As shown in
According to this comparative example, the duration of fire resistance was less than 2 minutes because R—COOH of poly(acrylic acid-co-maleic acid) did not react with unmodified Al2O3 to form a well-structured composite by the formation of chemical bonds.
Polyurethane containing R—NCO was dissolved or dispersed in hexane. Subsequently, unmodified inorganic particles SiO2 were added to the polymer solution, and the mixture was stirred at room temperature for 20 minutes. 1 mm-thick mixture slurry was coated on a teflon sheet, and then placed in an oven and molded at 60° C. for 120 minutes.
As shown in
According to this comparative example, the duration of fire resistance was about 2 minutes because R—NCO of polyurethane did not react with unmodified SiO2 to form a well-structured composite by the formation of chemical bonds.
Poly(vinyl alcohol) containing R—OH was dissolved or dispersed in water. Subsequently, inorganic particles Al(OH)3 were added to the polymer solution, and the mixture was stirred at 70-90° C. for 20 minutes. 1 mm-thick mixture slurry was coated on a teflon sheet, and then placed in an oven, dried at 60° C. for 60 minutes, 80° C. for 60 minutes, 100° C. for 60 minutes, 120° C. for 30 minutes, 140° C. for 30 minutes, 160° C. for 30 minutes, 180° C. for 30 minutes, and finally, molded at 200° C. for 240 minutes.
As shown in
According to this comparative example, the duration of fire resistance was less than 2 minutes because R—OH of poly(vinyl alcohol) did not react with the M-OH of Al(OH)3 to form a well-structured composite by the formation of chemical bonds.
Due to the chemical bonding between the corresponding reactive functional groups of the organic polymer and the inorganic particles, the formed char layer on the surface is firm with excellent structural integrity and does not easily crack or peel, effectively preventing direct heat transfer to the interior. The fire resistant material is not only flame retardant but also protective of interior materials. As a result, the fire resistance is significantly extended.
10 g of poly(ethylene-co-acrylic acid) was charged in a reactor, preheated to melt at 80-120° C. and then stirred at 300 rpm. 10.8 g of deionized water and 10.8 g of aqueous ammonia were added to the reactor, giving a white emulsion after stirring for 10 minutes. Subsequently, 10 g of aluminum hydroxide powder was added to the reactor, giving a white slurry after stirring for 10 minutes. The slurry was charged in a 100*100*2 mm teflon mold and then placed in an oven, dried at 60° C. for 60 minutes, 80° C. for 60 minutes, 100° C. for 60 minutes, 120° C. for 30 minutes, 140° C. for 30 minutes, 160° C. for 30 minutes, 180° C. for 30 minutes, and finally, molded at 200° C. for 240 minutes.
A 2 mm-thick molded plate was removed from the teflon mold, and placed on a piece of A4 size paper. A flame test was conducted on the surface of the fire-resistant plate by butane gas torch with flame temperature of 1000-1200° C. for 30 seconds to 3 minutes. The result of the burning phenomenon of the piece of A4 size paper is summarized in Table 2. No scorching was observed on the piece of A4 size paper after heating for 30, 60 and 120 seconds while it became slightly scorched after heating for 180 seconds.
According to this example, the duration of fire resistance was more than 3 minutes due to the strengthened sample layer, i.e. R—COOH of poly(ethylene-co-acrylic acid) reacted with M-OH of Al(OH)3 to form chemical bonds rather than physical blending.
10 g of poly(ethylene-co-acrylic acid) was charged in a reactor, preheated to melt at 80-120° C. and then stirred at 300 rpm. Subsequently, 10 g of aluminum hydroxide powder was added to the reactor, giving a white slurry after stirring for 10 minutes. The slurry was charged in a 100*100*2 mm teflon mold and then placed in an oven, dried at 60° C. for 60 minutes, 80° C. for 60 minutes, 100° C. for 60 minutes, 120° C. for 30 minutes, 140° C. for 30 minutes, 160° C. for 30 minutes, 180° C. for 30 minutes, and finally, molded at 200° C. for 240 minutes.
A 2 mm-thick molded plate was removed from the teflon mold, and placed on a piece of A4 size paper. A flame test was conducted on the surface of the fire-resistant plate by butane gas torch with flame temperature of 1000-1200° C. for 30 seconds to 3 minutes. The result of the burning phenomenon of the piece of A4 size paper is summarized in Table 2. No scorching was observed on the piece of A4 size paper after heating for 30, 60 and 120 seconds while it became slightly scorched after heating for 180 seconds.
According to this example, the duration of fire resistance was more than 3 minutes due to the strengthened sample layer, i.e. —COOH of poly(ethylene-co-acrylic acid) reacted with —OH of Al(OH)3 to form chemical bonds rather than physical blending.
20 g of poly(acrylic acid-co-maleic acid) (50 wt % solid content) was charged in a reactor, preheated at 80-90° C. and then stirred at 300 rpm. 10 g of aqueous ammonia were added to the reactor and stirred for 10 minutes. Subsequently, 10 g of aluminum hydroxide powder was added to the reactor, giving a yellow slurry after stirring for 10 minutes. The slurry was charged in a 100*100*2 mm teflon mold and then placed in an oven, dried at 60° C. for 60 minutes, 80° C. for 60 minutes, 100° C. for 60 minutes, 120° C. for 30 minutes, 140° C. for 30 minutes, 160° C. for 30 minutes, 180° C. for 30 minutes, and finally, molded at 200° C. for 240 minutes.
A 2 mm-thick molded plate was removed from the teflon mold, and placed on a piece of A4 size paper. A flame test was conducted on the surface of the fire-resistant plate by butane gas torch with flame temperature of 1000-1200° C. for 30 seconds to 3 minutes. The result of the burning phenomenon of the piece of A4 size paper is summarized in Table 2. No scorching was observed on the piece of A4 size paper after heating for 30, 60 and 120 seconds while it became slightly scorched after heating for 180 seconds.
According to this example, the duration of fire resistance was more than 3 minutes due to the strengthened sample layer, i.e. —COOH of poly(acrylic acid-co-maleic acid) reacted with —OH of Al(OH)3 to form chemical bonds rather than physical blending.
50 g of reactive polyurethane containing 8% reactive isocyanate groups was charged in a reactor and stirred at 300 rpm. Subsequently, 50 g of aluminum hydroxide powder was added to the reactor, giving a white slurry after stirring for 5 minutes. The slurry was charged in a 100*100*2 mm teflon mold and then dried at room temperature for 24 hours.
A 2 mm-thick molded plate was removed from the teflon mold, and placed on a piece of A4 size paper. A flame test was conducted on the surface of the fire-resistant plate by butane gas torch with flame temperature of 1000-1200° C. for 30 seconds to 3 minutes. The result of the burning phenomenon of the piece of A4 size paper is summarized in Table 2. No scorching was observed on the piece of A4 size paper after heating for 30, 60 and 120 seconds while it became slightly scorched after heating for 180 seconds.
According to this example, the duration of fire resistance was more than 3 minutes due to the strengthened sample layer, i.e. —NCO of reactive polyurethane reacted with —OH of Al(OH)3 to form chemical bonds rather than physical blending.
50 g of reactive polyurethane containing 8% reactive isocyanate groups was charged in a reactor and stirred at 300 rpm. Subsequently, 45 g of magnesium hydroxide powder and 5 g of modified nanoclay containing —OH groups (Cloisite 30B from Southern Clay Product Corp.) were added to the reactor, giving a white slurry after stirring for 5 minutes. The slurry was charged in a 100*100*2 mm teflon mold and then dried at room temperature for 24 hours.
A 2 mm-thick molded plate was removed from the teflon mold, and placed on a piece of A4 size paper. A flame test was conducted on the surface of the fire-resistant plate by butane gas torch with flame temperature of 1000-1200° C. for 30 seconds to 3 minutes. The result of the burning phenomenon of the piece of A4 size paper is summarized in Table 2. No scorching was observed on the piece of A4 size paper after heating for 30, 60 and 120 seconds while it became slightly scorched after heating for 180 seconds.
According to this example, the duration of fire resistance was more than 3 minutes due to the strengthened sample layer, i.e. —NCO of reactive polyurethane reacted with —OH of Mg(OH)3 and nanoclay to form chemical bonds rather than physical blending.
Referring to
According to this example, the duration of fire resistance was remarkably improved due to the strengthened sample layer, i.e. —NCO of reactive polyurethane reacted with —OH of Mg(OH)3 and nanoclay to form chemical bonds rather than physical blending.
50 g of reactive polyurethane containing 7.6% reactive isocyanate groups was charged in a reactor and stirred at 300 rpm. Subsequently, 50 g of modified titanium dioxide powder which carried —OH functional groups on the surface was added to the reactor, giving a white slurry after stirring for 5 minutes. The slurry was charged in a 100*100*2 mm teflon mold, dried at room temperature for 24 hours, and finally molded in an oven at 80° C. for 24 hours.
A 2 mm-thick molded plate was removed from the teflon mold, and placed on a piece of A4 size paper. A flame test was conducted on the surface of the fire-resistant plate by butane gas torch with flame temperature of 1000-1200° C. for 30 seconds to 3 minutes. The result of the burning phenomenon of the piece of A4 size paper is summarized in Table 2. No scorching was observed on the piece of A4 size paper after heating for 30, 60 and 120 seconds while it became slightly scorched after heating for 180 seconds.
According to this example, the duration of fire resistance was more than 3 minutes due to the strengthened sample layer, i.e. —NCO of reactive polyurethane reacted with —OH of modified TiO2 to form chemical bonds rather than physical blending.
40 g of reactive polyurethane containing 7.6% reactive isocyanate groups was charged in a reactor and stirred at 300 rpm. 50 g of modified titanium dioxide powder which carried —OH functional groups on the surface was added to the reactor and stirred for 3 minutes. Subsequently, 10 g of PPG 400 (polypropylene glycol; Mw=400) was added to the reactor, giving a white slurry after stirring for 2 minutes. The slurry was charged in a 100*100*2 mm teflon mold, dried at room temperature for 24 hours, and finally molded in an oven at 80° C. for 24 hours.
A 2 mm-thick molded plate was removed from the teflon mold and placed on a piece of A4 size paper. The plate had excellent flexibility, exhibiting a radius of curvature of about 3 cm. A flame test was conducted on the surface of the fire-resistant plate by butane gas torch with flame temperature of 1000-1200° C. for 30 seconds to 3 minutes. The result of the burning phenomenon of the piece of A4 size paper is summarized in Table 2. No scorching was observed on the piece of A4 size paper after heating for 30, 60 and 120 seconds while it became slightly scorched after heating for 180 seconds.
According to this example, the duration of fire resistance was more than 3 minutes due to the strengthened sample layer, i.e. —NCO of reactive polyurethane reacted with —OH of modified TiO2 to form chemical bonds rather than physical blending.
40 g of reactive polyurethane containing 8% reactive isocyanate groups was charged in a reactor and stirred at 300 rpm. Subsequently, 45 g of modified titanium dioxide powder which carried —OH functional groups on the surface and 5 g of modified nanoclay containing —OH groups (Cloisite 30B from Southern Clay Product Corp.) were added to the reactor and stirred for 3 minutes. Next, 10 g of PPG 400 (polypropylene glycol; Mw=400) was added to the reactor, giving a light yellow slurry after stirring for 2 minutes. The slurry was charged in a 100*100*2 mm teflon mold, dried at room temperature for 24 hours, and finally molded in an oven at 80° C. for 24 hours.
A 2 mm-thick molded plate was removed from the teflon mold and placed on a piece of A4 size paper. The plate had excellent flexibility, exhibiting a radius of curvature of about 3 cm. A flame test was conducted on the surface of the fire-resistant plate by butane gas torch with flame temperature of 1000-1200° C. for 30 seconds to 3 minutes. The result of the burning phenomenon of the piece of A4 size paper is summarized in Table 2. No scorching was observed on the piece of A4 size paper after heating for 30, 60 and 120 seconds while it became slightly scorched after heating for 180 seconds.
According to this example, the duration of fire resistance was more than 3 minutes due to the strengthened sample layer, i.e. —NCO of reactive polyurethane reacted with —OH of nanoclay and modified TiO2 to form chemical bonds rather than physical blending.
20 g of 3,4-epoxycyclohexyl methyl-3,4-epoxycyclohexane carboxylate (E4221, epoxy resin from Union Carbide) was charged in a reactor and stirred at 300 rpm, followed by addition of an excess amount (8 g, equivalence ratio of E4221/MeHHPA=1/1.14) of MeHHPA (hexahydro-4-methylphthalic anhydride) as curing agent and 0.1 g of BDMA (N,N-dimethyl benzylamine) as catalyst. After stirring for 5 minutes, 48.1 g of aluminum hydroxide powder was added to the reactor, giving a white slurry after stirring for 10 minutes. The slurry was charged in 100*100*2 mm and 100*100*4 mm teflon mold, dried at 120° C. for 1 hours.
2 mm and 4 mm-thick molded plates were removed from the teflon molds and placed on a piece of A4 size paper. A flame test was conducted on the surface of the fire-resistant plates by butane gas torch with flame temperature of 1000-1200° C. for 30 seconds to 3 minutes. The result of the burning phenomenon of the piece of A4 size paper is summarized in Table 2. For 2 mm-thick molded plate, no scorching was observed on the piece of A4 size paper after heating for 30 and 60 while it became slightly scorched after heating for 120 seconds, and scorched after heating for 180 seconds. For 4 mm-thick molded plate, no scorching was observed on the piece of A4 size paper after heating for 30, 60 and 120 seconds while it became slightly scorched after heating for 180 seconds.
According to this example, the duration of fire resistance was more than 3 minutes due to the strengthened sample layer, i.e. anhydride groups of epoxy resin (derived from excess MeHHPA) reacted with —OH groups of Al(OH)3 to form chemical bonds rather than physical blending.
50 g of reactive polyurethane containing 8% reactive isocyanate groups was charged in a reactor and stirred at 300 rpm. Subsequently, 50 g of unmodified silicon dioxide powder was added to the reactor, giving a white slurry after stirring for 5 minutes. The slurry was charged in a 100*100*2 mm teflon mold, then dried at room temperature for 24 hours, and finally molded in an oven at 80° C. for 24 hours.
A 2 mm-thick molded plate was removed from the teflon mold, and placed on a piece of A4 size paper. A flame test was conducted on the surface of the fire-resistant plate by butane gas torch with flame temperature of 1000-1200° C. for 30 seconds to 3 minutes. The result of the burning phenomenon of the piece of A4 size paper is summarized in Table 2. When the flame contacted the surface of the sample layer, the composite rapidly melted within several seconds and then charred irregularly in 30 seconds. The nonuniform char had lost its structural integrity due to the formation of cracks. A piece of A4 size paper became slightly scorched after heating for 30 seconds; scorched after heating for 60 seconds. Finally, the paper burned after heating for 120 seconds because of the majority of cracks.
According to this comparative example, the plate could not withstand a flame temperature of 1000-1200° C. because the unmodified SiO2 surfaces failed to react with —NCO of polyurethane to form a well-structured composite by the formation of chemical bonds.
50 g of polyurethane containing no reactive isocyanate group was charged in a reactor and stirred at 300 rpm. Subsequently, 50 g of aluminum hydroxide powder was added to the reactor, giving a white slurry after stirring for 5 minutes. The slurry was charged in a 100*100*2 mm teflon mold, then dried in an oven at 60° C. for 120 minutes, 80° C. for 120 minutes, 100° C. for 120 minutes, and finally molded at 120° C. for 360 minutes.
A 2 mm-thick molded plate was removed from the teflon mold, and placed on a piece of A4 size paper. A flame test was conducted on the surface of the fire-resistant plate by butane gas torch with flame temperature of 1000-1200° C. for 30 seconds to 3 minutes. The result of the burning phenomenon of the piece of A4 size paper is summarized in Table 2. When the flame contacted the surface of the sample layer, the composite rapidly melted within several seconds and then charred irregularly in 30 seconds. The nonuniform char had lost its structural integrity due to the formation of cracks. A piece of A4 size paper became scorched after heating for 30 seconds. Finally, the paper burned after heating for 60 seconds because of the majority of cracks.
According to this comparative example, the plate could not withstand a flame temperature of 1000-1200° C. because the polyurethane had no reactive functional group to react with —OH of aluminum hydroxide to form a well-structured composite by the formation of chemical bonds.
50 g of poly(vinyl alcohol) containing —OH groups was dissolved in water and then stirred at 300 rpm. Subsequently, 50 g of aluminum hydroxide powder was added to poly(vinyl alcohol), giving a white slurry after stirring at 70-90° C. for 20 minutes. The slurry was charged in a 100*100*2 mm teflon mold and then placed in an oven, dried at 60° C. for 60 minutes, 80° C. for 60 minutes, 100° C. for 60 minutes, 120° C. for 30 minutes, 140° C. for 30 minutes, 160° C. for 30 minutes, 180° C. for 30 minutes, and finally, molded at 200° C. for 240 minutes.
A 2 mm-thick molded plate was removed from the teflon mold, and placed on a piece of A4 size paper. A flame test was conducted on the surface of the fire-resistant plate by butane gas torch with flame temperature of 1000-1200° C. for 30 seconds to 3 minutes. The result of the burning phenomenon of the piece of A4 size paper is summarized in Table 2. When the flame contacted the surface of the sample layer, the composite rapidly melted within several seconds and then charred irregularly in 30 seconds. The nonuniform char had lost its structural integrity due to the formation of cracks. A piece of A4 size paper became slightly scorched after heating for 30 seconds; scorched after heating for 60 seconds. Finally, the paper burned after heating for 120 seconds because of the majority of cracks.
According to this comparative example, the plate could not withstand a flame temperature of 1000-1200° C. because —OH groups of aluminum hydroxide could not react with —OH groups of poly(vinyl alcohol) to form a well-structured composite by the formation of chemical bonds.
While the invention has been described by ways of examples and in terms of preferred embodiment, it is to be understood that the invention is not limited thereto. To the contrary, it is intended to cover various modifications and similar arrangements (as would be apparent to those skilled in the art). Therefore, the scope of the appended claims should be accorded the broadest interpretation so as to encompass all such modifications and similar arrangements.
| Number | Date | Country | Kind |
|---|---|---|---|
| 94146503 A | Dec 2005 | TW | national |
This application is a Continuation-In-Part of application Ser. No. 11/410,913, filed on Apr. 26, 2006, which claims priority to Taiwan Patent Application no. 94146503, filed on Dec. 26, 2005.
| Number | Name | Date | Kind |
|---|---|---|---|
| 3714047 | Marion et al. | Jan 1973 | A |
| 4150207 | Cenker et al. | Apr 1979 | A |
| 4376840 | Moriwaki et al. | Mar 1983 | A |
| 4748195 | Hackl et al. | May 1988 | A |
| 4876291 | Dallavia et al. | Oct 1989 | A |
| 5218027 | Smith et al. | Jun 1993 | A |
| 5418272 | Kawabata et al. | May 1995 | A |
| 5670748 | Gingue et al. | Sep 1997 | A |
| 5723515 | Gottfried | Mar 1998 | A |
| 5853809 | Campbell et al. | Dec 1998 | A |
| 6020419 | Bock et al. | Feb 2000 | A |
| 6262161 | Betso et al. | Jul 2001 | B1 |
| 6599631 | Kambe et al. | Jul 2003 | B2 |
| 6646205 | Hase et al. | Nov 2003 | B2 |
| 6815489 | Fischer et al. | Nov 2004 | B1 |
| 7053145 | Tasaka et al. | May 2006 | B1 |
| 20040054035 | Hallissy et al. | Mar 2004 | A1 |
| 20060014880 | Zhong et al. | Jan 2006 | A1 |
| 20060036006 | Heschke et al. | Feb 2006 | A1 |
| 20070149675 | Huang et al. | Jun 2007 | A1 |
| 20070149676 | Hu et al. | Jun 2007 | A1 |
| 20070149677 | Huang et al. | Jun 2007 | A1 |
| 20070179235 | Huang et al. | Aug 2007 | A1 |
| Number | Date | Country |
|---|---|---|
| 1262698 | Aug 2000 | CN |
| 1341141 | Mar 2002 | CN |
| 2854898 | Dec 1978 | DE |
| 2854898 | Jun 1980 | DE |
| 237758 | Jul 1986 | DE |
| 19941181 | May 2000 | DE |
| 1 100 093 | May 2001 | EP |
| 1 215 238 | Jun 2002 | EP |
| 1 215 685 | Jun 2002 | EP |
| 1384752 | Jan 2004 | EP |
| 1457523 | Sep 2004 | EP |
| 47-44351 | Nov 1972 | JP |
| 51022799 | Feb 1976 | JP |
| 57-92037 | Jun 1982 | JP |
| 59-42779 | Mar 1984 | JP |
| 61272222 | Dec 1986 | JP |
| 62-201934 | Sep 1987 | JP |
| 2-210717 | Aug 1990 | JP |
| 02202907 | Aug 1990 | JP |
| 4-55454 | Feb 1992 | JP |
| 04202587 | Jul 1992 | JP |
| 5-239281 | Sep 1993 | JP |
| 08113682 | May 1996 | JP |
| 09059509 | Mar 1997 | JP |
| 9-204824 | Aug 1997 | JP |
| 10029278 | Feb 1998 | JP |
| 10-120948 | May 1998 | JP |
| 10147707 | Jun 1998 | JP |
| 10-245456 | Sep 1998 | JP |
| 11080538 | Mar 1999 | JP |
| 11-306873 | Nov 1999 | JP |
| 11-310720 | Nov 1999 | JP |
| 2001-2840 | Jan 2001 | JP |
| 2002-179857 | Jun 2002 | JP |
| 2002-324442 | Nov 2002 | JP |
| 2003-96306 | Apr 2003 | JP |
| 2004254407 | Sep 2004 | JP |
| 2005-60675 | Mar 2005 | JP |
| 2005-162931 | Jun 2005 | JP |
| 2005-213480 | Aug 2005 | JP |
| 2005-232264 | Sep 2005 | JP |
| 442549 | Sep 1987 | TW |
| 397885 | Jul 1988 | TW |
| 499469 | Feb 1989 | TW |
| 583078 | Jun 1990 | TW |
| 419514 | Jan 2001 | TW |
| 200415235 | Aug 2004 | TW |
| 263628 | Oct 2006 | TW |
| WO-9927015 | Jun 1999 | WO |
| WO 2004035711 | Sep 2004 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 20070179235 A1 | Aug 2007 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 11410913 | Apr 2006 | US |
| Child | 11642627 | US |
