JP3087112B2 - Fireproof insulation panel - Google Patents

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a fireproof and heat-insulating panel which is lightweight, high-strength, excellent in heat insulation and fire resistance, and is particularly suitable for use in the outer walls of buildings or structures and in prefabricated refrigerated warehouses. It is.

[0002]

2. Description of the Related Art Panels used for buildings such as office buildings and public facilities or outer walls of the structures are described below.
According to the Building Standards Law, it is stipulated that the building should have a fireproof structure or a fireproof structure according to the size of the building, the purpose of use and whether the area is a fireproof area, and the fireproof test of JIS A 1304 or the fireproof test of the Ministry of Construction Notification No. 1675. It is required that the panel be a refractory panel that has passed the requirements.

Conventionally, in such a fire resistance test, a panel that can pass the fire resistance test for one hour mainly includes:
Panels using lightweight cellular concrete (hereinafter referred to as ALC) or sandwich panels in which ALC, calcium silicate, asbestos perlite plate, etc. are sandwiched between asbestos slate plates have been known.

However, the specific gravity of the ALC plate and the asbestos slate plate is high, and the plate thickness is large. Therefore, a dedicated sash is required, not only is the transportation cost high, but also labor is required during the construction, and the use of a crane or the like requires There was a problem that the construction cost also became high.

To solve this problem, several proposals have been made on lightweight panels having fire resistance. For example, JP-A-1-268944 discloses a vinyl chloride resin containing an inorganic filler or a chlorinated resin. A semi-combustible heat insulating core material made of a foam mainly composed of a vinyl chloride resin, and a skin material mainly composed of cement or mortar reinforced with an inorganic fiber reinforcing material on the outer surface side of the semi-combustible heat insulating core material; On the inner surface side of the semi-combustible heat insulating core material, a fire-resistant panel composed of a semi-combustible material or a plate material having incombustibility equal to or more than that is disclosed, and further, a fire-resistant panel similar to this, JP-A-2-26641 and JP-A-4-3
No. 53140 also discloses.

Japanese Patent Application Laid-Open No. Hei 2-273230 discloses that
In a sandwich panel in which an inorganic lightweight aggregate is finely packed as a core material between metal plates serving as front and back materials, a mixture of a urea resin prepolymer and a melamine resin prepolymer contains Na, P inside the front and back materials. , Al, Si, Zn, C
a thin layer of a mixed solution containing a powder of r, Mg, Fe or the like is provided, and the core material is bound with a polyisocyanurate resin foam or a phenol resin foam, and
There has been disclosed a fire-resistant composite panel in which the above-mentioned resin foam is filled in the gaps between the respective aggregates and these components are integrally formed. A similar fire-resistant composite panel is disclosed in Japanese Patent Application Laid-Open No. 2-273232. This is also disclosed in the official gazette.

Further, Japanese Patent Application Laid-Open No. 5-77348 discloses that
In a composite board in which a separation layer is interposed between a non-combustible base material and a resol type phenol resin foam serving as a core material, the separation layer is formed of a nonwoven fabric having a thickness of 0.1 mm or more made of heat-resistant synthetic fiber. Then, an adhesive layer of a component that reacts with water is interposed between the nonwoven fabric and the non-combustible substrate, and the nonwoven fabric is impregnated with an adhesive to be integrated. A composite plate characterized by self-adhesion at the time of foam formation and fixation by impregnation thereof is disclosed, and a similar sandwich plate is also disclosed in JP-A-5-96675.

Further, in Japanese Patent Application Laid-Open No. 7-1631,
A core material foam-hardened by mixing an inorganic material such as aluminum hydroxide, ammonium polyphosphate, graphite, calcium silicate or calcium carbonate into the resole type phenol resin foam between the face materials is integrally formed. A fire-resistant composite plate characterized by the above is disclosed, and a fire-resistant composite plate similar to this is also disclosed in JP-A-7-1632, JP-A-7-1633, and JP-A-7-1637. I have.

As described above, a conventional lightweight composite panel having fire resistance is made of a resin foam which is flame-retardant or self-extinguishing, such as a phenol resin foam, a vinyl chloride resin foam, a polyisocyanurate resin foam. Using the body as a core material,
Further, an inorganic filler is mixed in the resin foam, or a non-combustible skin material is used.

[0010]

However, although phenolic resin foams are flame-retardant, they have high friability,
Lack of adhesiveness to the skin material, peeling after construction may be a problem, and this is considered to be caused by the water generated during the foam hardening of the phenolic resin foam, which causes the foam structure to be roughened. In order to solve this problem, see, for example,
No. 348 discloses that a nonwoven fabric made of a heat-resistant fiber is provided between a skin material and a phenol resin foam,
A function to diffuse water generated during curing is given to this,
Furthermore, using an adhesive, a skin material, a nonwoven fabric as a separation layer,
A method for improving the adhesiveness of a phenolic resin foam is described.

When the phenolic resin foam is used as the core material of the panel as described above, it is preferable to perform a process for improving the adhesiveness between the skin material and the core material. Is complicated, and a problem of economic efficiency may occur.

The resole type phenol resin is p-
Although an organic acid such as toluenesulfonic acid is used as a curing catalyst, since the acid remains in the foam, there is a problem that corrosion of a metal in contact and discoloration of wood are caused. As described in JP-A-58-120644), the remaining organic acid is reacted with the epoxy resin and collected, thereby preventing the remaining acid from affecting other materials and modifying the foam. It is necessary.

However, since the epoxy resin is inferior in flame retardancy and low smoke generation property to the phenol resin, in order to maintain the flame retardancy of the foam, the amount of the epoxy resin added at the time of reforming is reduced. However, as a result, there is a problem that the collection of the organic acid becomes insufficient, and the effect of the remaining acid on other materials cannot be completely prevented.

Further, even if a vinyl chloride resin foam is used as a core material, a step of forming the foam first and then bonding the foam to the skin material is necessary. There are cases where complications and economic problems arise.

On the other hand, in consideration of the strength as the core material and the adhesion to the skin material, polyurethane resin foam or polyisocyanurate resin foam is preferable, but these have inferior fire resistance performance as compared with phenol resin foam. ,For this reason,
Even if flame retardants such as aluminum hydroxide, ammonium polyphosphate, graphite, etc. are added, a considerable amount of addition is required to satisfy the above fire resistance performance, so that the foam expands to a predetermined size. Or the cells in the foam are destroyed, and the heat insulating property and the adhesion to the skin material are reduced.

The present invention solves the above-mentioned problems of the prior art, and is lightweight, high-strength, excellent in heat insulation and fire resistance, and is especially used for the outer wall of a building or a building and a prefabricated refrigerated refrigerator. The purpose of the present invention is to provide a fire-resistant insulation panel suitable for use in such applications.

[0017]

Means for Solving the Problems In order to achieve the above-mentioned object, the structure of the fire-resistant heat-insulating panel adopted by the present invention is a fire-resistant heat-insulating panel in which a core material made of a resin foam is covered with a skin material. The resin foam comprises an epoxy resin having two or more epoxy groups in a molecule and at least one selected from phosphoric acid, polyphosphoric acid and phenylphosphonic acid.
A composition comprising a kind of phosphoric acid, a foaming agent, and a foam stabilizer, wherein the ratio of the number of hydroxyl groups of the phosphoric acid to the number of epoxy groups of the epoxy resin is 0.4 to 1.0. And the aldehyde-based condensable resin is selected from among metal hydroxides and metal oxide hydrates in an amount of 5 to 200 parts by weight based on 100 parts by weight of the epoxy resin. At least one flame retardant is contained in an amount of 10 to 300 parts by weight based on 100 parts by weight of the epoxy resin.

In order to achieve the above object, the present invention also provides a fire-resistant heat insulating panel comprising a core material made of a resin foam, the surface of which is covered with a skin material. An epoxy resin having two or more epoxy groups in a molecule thereof, at least one phosphoric acid selected from phosphoric acid, polyphosphoric acid and phenylphosphonic acid, and a phosphate and a phosphoric acid having a hydroxyl group bonded to a phosphorus atom A composition comprising a mixture of at least one phosphoric acid compound selected from acid esters, a foaming agent, and a foam stabilizer is prepared by adding the phosphoric acid and the hydroxyl group of the phosphoric acid compound to the number of epoxy groups of the epoxy resin. A resin skeleton which is reacted at a usage ratio of 0.4 to 1.0, and the aldehyde-based condensable resin is mixed with the epoxy resin 100 And 5-200 parts by weight relative to the amount unit,
At least one flame retardant selected from a metal hydroxide and a metal oxide hydrate is contained in an amount of 10 to 300 parts by weight based on 100 parts by weight of the epoxy resin.

[0019]

BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail with reference to specific examples.

The epoxy resin for producing a resin foam in the present invention is a compound having two or more epoxy groups in a molecule, and a compound which can be cured by reacting with a curing agent for epoxy resin. In other words, this compound is a compound also referred to as a main component of an epoxy resin or a polyepoxide.

As the epoxy resin, a compound having a glycidyl group as an epoxy group is preferable, and a glycidyl ether-based epoxy resin is particularly preferable. However, the epoxy resin is not limited thereto. For example, a cycloaliphatic epoxy resin, glycidyl ester Epoxy resin, heterocyclic aliphatic epoxy resin, linear aliphatic epoxy resin, etc. (these epoxy resins may be oligomeric)
May be used, and one of these epoxy resins may be selected, or two or more thereof may be used in combination.

The epoxy resin is preferably a liquid at room temperature in view of the ease of mixing with the flame retardant and the fluidity at the time of foaming.
Glycidyl ether epoxy resins such as bisphenol A diglycidyl ether epoxy resin, bisphenol F diglycidyl ether epoxy resin, resorcin diglycidyl ether epoxy resin, phenol novolak polyglycidyl ether epoxy resin, cresol novolac polyglycidyl ether epoxy resin Glycidyl ester epoxy resins such as hexidyl phthalate epoxy resin and dimer acid glycidyl ester epoxy resin; 3,4-epoxy-6-methylcyclohexylmethyl carboxylate and 3,4-epoxycyclohexylmethyl carboxylate And other cyclic aliphatic epoxy resins.

The phosphoric acid for producing the resin foam in the present invention comprises at least one selected from phosphoric acid, polyphosphoric acid and phenylphosphonic acid, and the phosphoric acid reacts with the epoxy resin. In addition to forming the skeleton of the resin foam, it is also a component that imparts flame retardancy to the resin foam.

Among the above phosphoric acids, phosphoric acid is not particularly limited.
%, 85%, or 89%.

Various grades of polyphosphoric acid are commercially available depending on the content of P ₂ O ₅ .
It can be used without particular limitation, and there is no limitation on phenylphosphonic acid.

As the phosphoric acids, at least one of phosphoric acid, polyphosphoric acid and phenylphosphonic acid may be used, but two or more of them may be used. still,
Since phenylphosphonic acid among the above is a solid, it is preferable to use it in combination with phosphoric acid or polyphosphoric acid, which is a liquid, in order to easily flow during foaming and curing.

It is considered that the above-mentioned phosphoric acid reacts with the epoxy group of the epoxy resin and is taken into the molecular skeleton of the epoxy resin. Therefore, the phosphoric acid is obtained by controlling the amount of the phosphoric acid to an appropriate amount. Phosphoric acids can be prevented from remaining as free acids in the resulting foam. Therefore, by performing such control, even when the epoxy resin foam used as the core material of the fire-resistant insulation panel of the present invention is bonded to other materials such as metal and wood, for example, corrosion to the metal and discoloration to the wood are prevented. No need for neutralizing agents to prevent.

On the other hand, since phosphoric acid reacts rapidly with the epoxy group of the epoxy resin, as described later, both can react by simply mixing to form a foam. However, in some cases, the calorific value due to a rapid reaction with an epoxy group becomes too large, and foaming (vaporization) occurs at once depending on the type of a foaming agent, so that a dense foam may not be formed. In such a case, at least one type of phosphoric acid selected from a phosphate having a hydroxyl group bonded to a phosphorus atom and a phosphoric acid ester is used together with the phosphoric acid in order to control the reaction and suppress the heat generation. It is preferable to use a compound (hereinafter, sometimes simply referred to as a phosphoric acid compound) in combination.

In the present invention, by using the above phosphoric acid compound in combination, the reaction with the epoxy group is controlled to suppress the calorific value, and a good foam can be produced. Since it is also a component that imparts flame retardancy to the resin foam, even if it is used in a relatively large amount with respect to the phosphoric acids, there is little risk of lowering the flame retardancy of the obtained resin foam.

In the above phosphoric acid compound, at least one hydroxyl group bonded to a phosphorus atom is required to react with the epoxy group of the epoxy resin. At least one of them may be used, but two or more of them may be used.

Examples of the phosphate include ammonium dihydrogen phosphate, diammonium hydrogen phosphate, sodium dihydrogen phosphate, disodium hydrogen phosphate, potassium dihydrogen phosphate, dipotassium hydrogen phosphate, and phosphoric acid Examples thereof include calcium dihydrogen, calcium monohydrogen phosphate, aluminum dihydrogen phosphate, and dialuminum hydrogen phosphate. Examples of the phosphate include, for example, monomethyl phosphate, dimethyl phosphate, monoethyl phosphate, diethyl phosphate, monopropyl phosphate, monoisopropyl phosphate, monobutyl phosphate, monolauryl phosphate, monostearyl phosphate, mono-2-ethylhexyl phosphate. And monoisodecyl phosphate.

In the present invention, the phosphoric acid is used in such an amount that the ratio of the number of hydroxyl groups of the phosphoric acid to the number of epoxy groups of the epoxy resin is 0.4 to 1.0. When the amount used is less than 0.4 in the above ratio, the reaction heat generated by the reaction with the epoxy resin is small, the foaming (vaporization) of the foaming agent becomes insufficient, and the foam having a desired foaming ratio is obtained. It is difficult to obtain. When the amount of the phosphoric acid exceeds 1.0 in the above ratio, the phosphoric acid often becomes excessive and the ratio of remaining as a free acid in the foam becomes high. The foaming state of the body deteriorates, and when the foam comes into contact with metal or wood, the risk of corrosion and discoloration of the foam increases.

The amount of the phosphoric acid used is preferably adjusted to a more appropriate amount depending on the use of the foam, the production method, the production conditions, etc., and the workability during foaming, the mechanical strength of the foam, and the heat insulation properties From the uniformity of the above, the above ratio is 0.4 to 0.1.
More preferably, an amount of 8 is used.

When the above phosphoric acid compound is used in combination,
The total amount of the phosphoric acid and the phosphoric acid compound is such that the ratio of the total number of the hydroxyl groups of the phosphoric acid and the phosphoric acid compound to the number of the epoxy groups of the epoxy resin is 0.4 to 1.0.

The amount of the phosphoric acid compound to be used with respect to the phosphoric acids can be selected in accordance with the use of the foam, the production method, the production conditions and the like in the same manner as described above. It can be adjusted appropriately so as to obtain the curing time. Although not particularly limited, the ratio of the phosphoric acid to the total amount of the phosphoric acid and the phosphoric acid compound is preferably 40% by weight or more, and when the amount of the phosphoric acid is too small, the reactivity with the epoxy resin is insufficient. May occur.

When a solid phosphoric acid compound is used, it is preferable to use it in combination with a liquid phosphoric acid or polyphosphoric acid in order to facilitate the flow during foaming and curing.

In the present invention, the ratio of the number of hydroxyl groups of the phosphoric acid to the number of epoxy groups of the epoxy resin is a value obtained by dividing the number of hydroxyl groups of the phosphoric acid by the number of epoxy groups of the epoxy resin. The number of epoxy groups in the epoxy resin is the value obtained by dividing the amount of the epoxy resin used by the epoxy equivalent of the epoxy resin.When two or more epoxy resins are used, the It means the sum of the values obtained by dividing the amount used by the epoxy equivalent of each epoxy resin, and the number of hydroxyl groups of phosphoric acids is the value obtained by dividing the amount of phosphoric acid used by the hydroxyl equivalent of phosphoric acids. Yes, when two or more phosphoric acids are used, this is the total value obtained by dividing the amount of each phosphoric acid used by the hydroxyl equivalent of each phosphoric acid. If the same is true.

Here, the epoxy equivalent is a value obtained by dividing the average molecular weight of the epoxy resin by the number of epoxy groups per molecule, and the hydroxyl equivalent is the formula weight of the phosphoric acid or the phosphoric acid compound bonded to the phosphorus atom. It is the value divided by the number of hydroxyl groups.

The aldehyde-based condensable resin used in the present invention is a compound in which a methylol group in a molecule is condensed by heating or the like to crosslink and cure, and for example, has one or more methylol groups in the molecule. A resole type phenol resin or amino resin can be mentioned.

The resole type phenol resin includes:
For example, phenol, cresol, xylenol, 1 mole of phenols such as resorcinol, 1 to 3 moles of a compound obtained by adding formaldehyde can be mentioned,
Further, a resol type phenol resin obtained by precondensing the nucleus by precondensation can be used without any problem if it is in the B-stage state.

Examples of the amino resin include urea, melamine, benzoguanamine, acetoguanamine,
For 1 mol of glycouril, spiroganamin, etc.,
Compounds obtained by adding 1 to 3 mol of formaldehyde can be used.

However, even in the case of an amino resin, a compound obtained by adding formaldehyde to urea or the like and then etherifying a methylol group, for example, a compound such as hexamethoxymethylated melamine or the like can be used in combination with an epoxy resin described later and phosphoric acid. In some cases, the curing reaction may not easily proceed with the reaction heat of the reaction described above, and methanol generated from hexamethoxymethylated melamine or the like during the curing reaction may adversely affect the foaming state of the foam. It is preferable to avoid using amino resins whose groups have been etherified.

Further, among the aldehyde-based condensable resins, those in a liquid state contain an organic solvent or water as a solvent, and when the organic solvent has an adverse effect on the foaming state of the foam, or when the water contains Since the curing reaction may be hindered, it is preferable to use a solid or powdery aldehyde-based condensable resin containing no organic solvent or water.

In the present invention, the aldehyde-based condensable resin is used in an amount of 5 to 200 parts by weight per 100 parts by weight of the epoxy resin.
Although it is used in the range of parts by weight, in order to prevent water generated in the course of the condensation curing reaction of the aldehyde-based condensable resin from adversely affecting the foaming state of the foam, it is preferably 30 to 30 parts by weight.
Preferably, it is used in the range of 100 parts by weight.

When the amount of the aldehyde-based condensable resin is 5
When the amount is less than 10 parts by weight, the effect of improving the flame retardancy of the foam by adding the aldehyde-based condensable resin is insufficient. The effect of improving the properties is not so large relative to the addition amount, and rather, the fluidity of the epoxy resin or the like at the time of foaming may be reduced, and a foam having a desired size may not be obtained.

Examples of the flame retardant used in the present invention include metal hydroxides such as aluminum hydroxide, calcium hydroxide, zirconium hydroxide, cerium hydroxide and magnesium hydroxide, and calcium aluminate and silica. Calcium oxide, zinc silicate or montmorillonite, wollastonite, willemite, hectorite, saponite, talc, pyrophyllite, vermiculite, mica, at least selected from metal oxide hydrates including clay minerals such as dawsonite One type can be mentioned, but among these, aluminum hydroxide is preferably used because of its large endothermic effect.

In the present invention, the flame retardant is used in the range of 10 to 300 parts by weight with respect to 100 parts by weight of the epoxy resin. However, the moldability, flame retardancy, fire resistance and mechanical properties of the resulting foam are obtained. 30 from the viewpoint of balance of target strength
More preferably, it is used in the range of 250 parts by weight.

If the amount of the flame retardant is less than 10 parts by weight, the flame retardancy and fire resistance of the foam cannot be improved. The fluidity of the mixture at the time decreases, so that a foam of a predetermined shape cannot be obtained, and the density of the foam increases and the weight increases. However, the heat-insulating property cannot be improved, and rather, the heat insulation performance is deteriorated due to the destruction of the cells of the foam, embrittlement and poor adhesion to the skin material are caused.

Further, the flame retardant has an average particle diameter of 1 to 3.
The thickness is preferably 5 μm from the viewpoint of easy kneading to the resin and uniform dispersion in the foam.
More preferably, the thickness is 00 μm.

If the average particle size of the above-mentioned flame retardant is less than 1 μm, the bulk becomes so high that the handleability and the kneading to the resin may be poor, and the fluidity at the time of foaming is lacking. The problem may arise. On the other hand, when the average particle size is 30
If it exceeds 0 μm, the formation of cells of the foam may be hindered, the closed cell ratio may decrease, the thermal conductivity may increase, and the heat insulating property may decrease. or it refers to a value [50% value of the cumulative distribution] of been D ₅₀ measured by a dry sieve analysis.).

In the production of the epoxy resin foam described below, a part of the flame retardant is incorporated into the resin skeleton of the epoxy resin foam, and the remainder is dispersed in the epoxy resin foam. It is thought that there is.

Examples of the foaming agent for producing the resin foam of the present invention include known ones such as halogenated hydrocarbons and hydrocarbons. Halogenated hydrocarbons are preferred, and halogenated hydrocarbons which are liquid at room temperature are particularly preferred. These foaming agents can be used alone or as a mixture of two or more.

The halogenated hydrocarbons include, for example, chlorinated hydrocarbons such as methylene chloride and trichloroethylene; 2,2-dichloro-1,1,1-trifluoroethane (HCFC123), 1,1-dichloro -11-fluoroethane (HCFC141b), 1,1-dichloro-2,2,3,3,3-pentafluoropropane (HC
FC225ca), 1,3-dichloro-1,1,2,2
2,3-pentanefluoropropane (HCFC225c
b) chlorinated fluorinated hydrocarbons such as 1,1,1,2,2
3,3-hexafluoropropane (HFC236e
a) and fluorinated hydrocarbons such as 1,1,1,3,3-pentafluoropropane (HFC245fa).

[0054] Hydrocarbons such as pentane and cyclohexane, and ethers such as petroleum ether and isopropyl ether can also be used as the foaming agent. It is not preferable to use a flammable foaming agent as described above.

In the present invention, the foaming agent is preferably used in a range of 1 to 50 parts by weight based on 100 parts by weight of the epoxy resin. If the amount is less than 1 part by weight, the foaming is insufficient. When the content exceeds 50 parts by weight, the number of open cells increases, the closed cell ratio decreases, and the rigidity and heat insulation of the foam decrease.

Further, since the expansion ratio and density of the foam are changed by increasing or decreasing the amount of the foaming agent used, the amount of the foaming agent is adjusted so that the foam density required according to the use of the foam is obtained. Adjustment is preferred.

Examples of the foam stabilizer for producing the resin foam in the present invention include known ones used for producing various resin foams such as polyurethane resin foam and phenol resin foam. be able to.

The foam stabilizer is preferably a surfactant, and more preferably a nonionic surfactant. These foam stabilizers may be used alone or in combination of two or more.

Examples of the nonionic surfactant which can be used as the above-mentioned foam stabilizer include sorbitan esters such as sorbitan monostearate, sorbitan monooleate, polyoxyethylene sorbitan monostearate, and polyoxyethylene sorbitan monooleate. Polyethylene glycol esters such as polyethylene glycol monostearate, polyethylene glycol monosoleate, polyethylene glycol distearate, and polyethylene glycol dioleate; polyoxyethylene alkyl ethers other than those described above; polyoxyethylene alkyl esters; polyoxyethylene Alkylphenyl ethers; polyoxyethylene alkylphenyl esters, dimethylpolysiloxane polyoxyalkylene copolymers, etc. It can gel.

In the present invention, it is desirable to use the foam stabilizer in an amount of 0.01 to 10 parts by weight, more preferably 0.5 to 5 parts by weight, based on 100 parts by weight of the epoxy resin. If the amount is less than 0.01 part by weight, the effect of uniformizing the size and distribution of foam after foaming is lacking, and if it exceeds 10 parts by weight, it acts as a plasticizer and reduces the rigidity of the foam. Would.

In producing the epoxy resin foam of the present invention, in addition to the above-mentioned flame retardants, fillers, pigments, etc. are used for the purpose of adjusting the fluidity at the time of foaming hardening and for economical effects. These may be mixed with an epoxy resin or the like according to a standard method and used.

Since a composition containing an epoxy resin and phosphoric acid or the like usually reacts at room temperature, the method for producing an epoxy resin foam used as a core material of a fire-resistant and heat-insulating panel of the present invention requires an epoxy resin and a phosphorous-containing material. It is preferable that a mixture of an acid or a mixture of a phosphoric acid and a phosphoric acid compound (hereinafter, sometimes simply referred to as phosphoric acid or the like) is mixed at room temperature to form a reactive composition. In such a case, the mixing of the epoxy resin and phosphoric acid or the like can be performed under heating.

The aldehyde-based condensable resin, the flame retardant, the foaming agent and the foam stabilizer can be mixed with these at the same time when they are mixed. , A flame retardant, a foaming agent and a foam stabilizer can be mixed in advance, and if mixed in advance, the mixture is mixed with a component containing an epoxy resin to obtain a premix from the ease of mixing. And a component containing phosphoric acid or the like are preferably mixed to form a reactive composition.

In particular, since the flame retardant is a powder, it is preferable to mix it with a component containing an epoxy resin in advance in order to improve the fluidity of the composition during foaming and dispersion in the foam. These can be mixed using a kneader, a mixing roll, a Henschel mixer or the like.

A reactive composition containing an aldehyde-based condensable resin such as an epoxy resin, phosphoric acid, etc., a flame retardant, a foaming agent and a foam stabilizer can initiate a reaction at room temperature, and the reaction is accompanied by heat generation. As the foaming progresses, the foaming agent vaporizes and foams, reacts and cures to form an epoxy resin-based foam. Examples of a device for mixing and discharging such a component and ejecting the composition include a polyurethane resin foam and the like. It is preferred to use a mixing device called a multi-component mixing foaming machine as is usually used for the production of.

In the fire-resistant and heat-insulating panel of the present invention, a metal plate, an inorganic board, or the like can be used as the skin material. Examples of the metal plate that can be used as the skin material include a steel plate, an aluminum plate, and the like. . The metal plate may be subjected to painting or surface treatment for improving the appearance and preventing corrosion. Further, as the inorganic board, a gypsum board, an asbestos cement board, a calcium silicate board, a slag gypsum board, an ALC board, and the like can be used. Among these skin materials, the fire resistance of the panel is secured, and A steel plate is preferably used in that the thickness of the skin material is reduced to reduce the weight.

As a method for coating the resin foam with the skin material, an epoxy resin, phosphoric acid, or the like is provided between the two skin materials in the same manner as in a conventional sandwich panel manufacturing method using a polyurethane resin foam. A method of injecting a reactive composition containing an aldehyde-based condensable resin, a flame retardant, a foaming agent and a foam stabilizer, bonding the skin material and the foam at the same time as foaming and curing, and the reactive composition There is a method in which a board-shaped epoxy resin foam is manufactured by foaming and curing in advance, and then bonded to a skin material using a thermosetting adhesive or a hot melt adhesive. To achieve this, the former method is preferable.

The thickness of the fire-resistant and heat-insulating panel of the present invention is not particularly limited, and is preferably set appropriately according to the purpose of use and the structure of the building or building. That is, for example, if used in a prefabricated refrigerated warehouse, 50-
The thickness is preferably 150 mm, and when used as an outer wall of a building or a building, the thickness is preferably 25 to 100 mm in consideration of workability during construction. When the thickness of the fire-resistant insulation panel of the present invention is less than 25 mm, it tends to be difficult to maintain the performance that passes the fire resistance of one hour in the fire resistance test of JIS A 1304.

Next, an example of the method for manufacturing the fire-resistant and heat-insulating panel of the present invention will be specifically described.

First, a powdery or solid aldehyde-based condensable resin 5 to 100 parts by weight of an epoxy resin was used.
200 parts by weight and 10 to 300 parts by weight of a flame retardant having an average particle size of 1 to 300 μm are added and mixed with stirring. At this time, when the average particle diameter is relatively large, the apparent viscosity of the mixture may increase or the flame retardant may settle,
On the other hand, these can be prevented by using an ammonium salt or an amide-based surfactant as a dispersant, or by previously treating the surface of the flame retardant with stearic acid or a silane coupling agent. When the surfactant is used in an amount of 5 parts by weight or less, or when a surface-treated flame retardant is used, it does not affect foaming and curing of the resin foam at all, but the surface-treated flame retardant is used. More preferred.

Next, 0.01 to 10 parts by weight of a foam stabilizer and 1 to 50 parts by weight of a foaming agent are mixed. The apparatus used at this time is preferably a closed stirring tank provided with a cooling tower and capable of further cooling. The cooling tower is necessary to collect and cool the vaporized foaming agent to liquefy it by cooling, and to return the mixture back into the mixture.In addition to cooling the stirring layer, the cooling tower is used to vaporize the foaming agent due to heat generated during stirring and mixing. Useful to prevent loss. That is, considering the viscosity of the mixture and the vaporization of the foaming agent, the temperature of the stirring tank during stirring and mixing is 25 to 3
It is more preferable to control the temperature in the range of 0 ° C.

Usually, when handling epoxy resin, 40
Heating to ５０50 ° C. to improve the fluidity and transfer from the container to the stirring tank is performed, but this is not preferred in the present invention. This is because, when cooled in the stirring tank, the portion close to the tank is cooled immediately, but the viscosity increases and the stirring becomes insufficient, causing a phenomenon that the center part is not cooled. This is because there is a possibility of vaporization.

In order to easily mix the epoxy resin and the flame retardant, the epoxy resin and the foaming agent are mixed first,
A method of adding a flame retardant after lowering the viscosity of the epoxy resin may be selected.

The mixture obtained here is placed as a component X in a raw material tank of a multi-component mixing and foaming machine. Then, in order to adjust the foaming and curing time of the resin foam, a predetermined ratio of phosphoric acid is set. And a phosphoric acid compound as a Y component into another raw material tank.

Next, a frame, a spacer, and a skin material are pre-assembled, a sandwich panel frame provided with several injection ports is prepared, and a nozzle head of a multi-component mixing and foaming machine is inserted into the injection ports, and the X component and the Y component are inserted. Are mixed at a predetermined mixing ratio and simultaneously injected into the sandwich panel frame. At this time, it is not necessary to heat the sandwich panel frame, and by heating it in the opposite direction, the foaming agent may evaporate before the reaction between the epoxy resin and phosphoric acid, and a dense foam cannot be obtained. There are cases.

After completion of the foaming and curing, it is more preferable to cure the resin foam after foaming and curing by utilizing the reaction heat of the resin foam. And stress can be eliminated,
The adhesion between the skin material or the frame and the resin foam is further improved.

Further, one skin material is continuously supplied, and a reactive composition obtained by mixing the X component and the Y component at a predetermined ratio is applied to the back surface of the skin material by a multi-component mixing foaming machine. Immediately after that, the other skin material is supplied at a predetermined interval to sandwich the composition, the foam is continuously foamed between the two skin materials, and after the curing is completed, a method of cutting to a predetermined size with a cutter may also be selected. it can.

[0078]

The composition of the epoxy resin and phosphoric acid reacts rapidly at room temperature to generate heat. By utilizing the heat of reaction for vaporizing the foaming agent, the epoxy resin used in the present invention can be used. The system foam can be produced by easily and quickly curing a composition of an epoxy resin and phosphoric acids at room temperature without heating.

Further, since phosphoric acids and the like react and are taken into the resin skeleton constituting the epoxy resin foam used in the present invention, the phosphoric acids and the like function in the same manner as the reactive flame retardant, and It is possible to obtain an epoxy resin-based foam having high property.

Further, since a part of the flame retardant reacts with phosphoric acid or the like and is incorporated into the resin skeleton constituting the epoxy resin foam, the flame retardant and the residual flame retardant which have not been incorporated are taken into account. Has good wettability, and a larger amount of a flame retardant can be dispersed in a foam without destroying cells as compared with a conventional resin foam.

The flame retardancy of the resin foam can be further enhanced by combining an aldehyde-based condensable resin having low flammability among organic materials with an epoxy resin. Since it also acts as a curing catalyst for the resin, the curing reaction of the aldehyde-based condensable resin proceeds sufficiently without heating due to the heat of reaction between the epoxy resin and phosphoric acids.

By using the epoxy resin foam having the above-mentioned characteristics as a core material of a fire-resistant heat insulating panel, the heat insulating property is high, and the adhesive property of the epoxy resin is high by utilizing the adhesive property of the epoxy resin. A fire-resistant insulation panel can be obtained. Furthermore, when the fire-resistant insulation panel is exposed to a high temperature due to a flame or the like, the flame retardant absorbs heat by dehydrating or releasing water of crystallization at around 200 to 500 ° C. The temperature rise of the heat insulating panel and the heat transfer to the opposite surface can be suppressed.

Further, phosphoric acids and the like incorporated in the resin skeleton constituting the epoxy resin foam used in the present invention also act as a dehydration and carbonization accelerator when exposed to the above high temperatures. Promotes the release of water from the resin skeleton,
Since the non-combustible heat-insulating layer is formed by the carbonized cells, heat transfer to the opposite surface of the refractory heat-insulating panel can be suppressed even after being exposed to a high temperature.

By the above operation, the insulated fireproof panel of the present invention provides a fireproof structure test (JIS A 13) for building structural parts.
04) One hour of fire resistance can be provided.

[0085]

The present invention will be described in more detail with reference to the following examples.

Example 1 100 parts by weight of a phenol novolak polyglycidyl ether epoxy resin having an epoxy equivalent of 175 g / eq and a molecular weight of about 600, 1,1-dichloro-1- as a foaming agent
15 parts by weight of fluoroethane, and 3 parts by weight of a dimethylpolysiloxane polyoxyalkylene copolymer as a foam stabilizer were put into a stirring tank equipped with a cooling tower, and thoroughly stirred and mixed.
50 parts by weight of an amino resin as an aldehyde-based condensable resin obtained by adding 2.2 mol of formaldehyde to 1 mol of melamine, and an average particle diameter of 30 μm as a flame retardant
Was added and mixed. This mixture was designated as X component and put in a raw material tank of a multi-component mixed foaming machine. Next, 89% phosphoric acid for industrial use was used as the Y component and placed in another raw material tank.

On the other hand, two color steel plates each having a thickness of 0.4 mm as a skin material and four aluminum frames each having a thickness of 2 mm and a height of 50 mm were assembled, and 1000 mm × 1000 mm having injection holes provided at four corners. A sandwich panel frame of × 50 mm was prepared. Subsequently, the respective components X and Y were fed into the mixing head of the multi-component mixing and foaming machine at a total flow rate of 3 kg / min at a discharge weight ratio of X: Y = 100: 6.3. This corresponds to 0.8 in the ratio of the number of hydroxyl groups of phosphoric acid to the number of epoxy groups of the epoxy resin. 7,500 g of this reactive composition was immediately injected into the above sandwich panel frame at room temperature from an injection port and foamed. Foaming started 45 seconds after injection and foam hardening was completed 5 minutes later. After that, the panel was left to cool naturally.

Example 2 100 parts by weight of a phenol novolak polyglycidyl ether-based epoxy resin having an epoxy equivalent of 175 g / eq and a molecular weight of about 600, and 1,1-dichloro-1- as a foaming agent
15 parts by weight of fluoroethane, and 3 parts by weight of a dimethylpolysiloxane polyoxyalkylene copolymer as a foam stabilizer were put into a stirring tank equipped with a cooling tower, and thoroughly stirred and mixed.
50 parts by weight of a resole-type phenol resin as an aldehyde-based condensable resin obtained by adding 2.5 moles of formaldehyde to 1 mole of phenol, and 120 parts by weight of bentonite having an average particle diameter of 80 μm as a flame retardant were added and mixed. did. This mixture was designated as X component and put in a raw material tank of a multi-component mixed foaming machine. Next, 89% phosphoric acid for industrial use was used as the Y component and placed in another raw material tank.

On the other hand, two color steel plates each having a thickness of 0.4 mm as a skin material and four aluminum frames each having a thickness of 2 mm and a height of 50 mm were assembled, and 1000 mm × 1000 mm having injection holes provided at four corners. A sandwich panel frame of × 50 mm was prepared. Subsequently, the respective components X and Y were fed into the mixing head of the multi-component mixing and foaming machine at a total flow rate of 3 kg / min at a discharge weight ratio of X: Y = 100: 6.3. This corresponds to 0.8 in the ratio of the number of hydroxyl groups of phosphoric acid to the number of epoxy groups of the epoxy resin. 7,500 g of this reactive composition was immediately injected into the above sandwich panel frame at room temperature from an injection port and foamed. Foaming started 40 seconds after injection, and foam hardening was completed 3 minutes later. After that, the panel was left to cool naturally.

Example 3 100 parts by weight of a phenol novolak polyglycidyl ether epoxy resin having an epoxy equivalent of 175 g / eq and a molecular weight of about 600, and 1,1-dichloro-1 as a foaming agent
-15 parts by weight of fluoroethane and dimethylpolysiloxane polyoxyalkylene copolymer 3 as a foam stabilizer
After putting parts by weight into a stirring tank with a cooling tower and mixing well,
50 parts by weight of an amino resin as an aldehyde-based condensable resin obtained by adding 2.2 mol of formaldehyde to 1 mol of melamine, and an average particle diameter of 60 μm as a flame retardant
Of bentonite was added and mixed. This mixture was designated as X component and put in a raw material tank of a multi-component mixed foaming machine. Next, a mixture of industrial 89% phosphoric acid and monoethyl phosphate at a molar ratio of 1: 1 and a weight ratio of 0.7: 1 was used as the Y component and placed in another raw material tank.

On the other hand, two color steel plates each having a thickness of 0.4 mm as a skin material and four aluminum frames each having a thickness of 2 mm and a height of 50 mm were assembled, and 1000 mm × 1000 mm having injection holes at four corners. A sandwich panel frame of × 50 mm was prepared. Subsequently, the respective components X and Y were fed into the mixing head of the multi-component mixed foaming machine at a total flow rate of 3 kg / min at a discharge weight ratio of X: Y = 100: 9.6. This corresponds to a ratio of the number of hydroxyl groups of phosphoric acid and monoethyl phosphate to the number of epoxy groups of the epoxy resin of 1.0. 7,500 g of this reactive composition was immediately injected into the above sandwich panel frame at room temperature from an injection port and foamed. Foaming is 45 after injection
Starting in seconds, the foam hardening was complete after 5 minutes. After that, the panel was left to cool naturally.

Example 4 A phenol novolak polyglycidyl ether-based epoxy resin having an epoxy equivalent of 175 g / eq and a molecular weight of about 600 and a bisphenol F diglycidyl ether-based epoxy resin having an epoxy equivalent of 175 g / eq in a weight ratio of 4: 1.
100 parts by weight of the mixed resin mixed with 1,
15 parts by weight of 1-dichloro-2,2,3,3,3-pentafluoropropane and 2 parts by weight of polyoxyethylene sorbitan monostearate as a foam stabilizer were put into a stirring tank equipped with a cooling tower and mixed well. Thereafter, 2.5 mol of formaldehyde was added to 1 mol of phenol, 100 parts by weight of a resol type phenol resin as an aldehyde-based condensable resin, and an average particle diameter of 10 μm subjected to a surface treatment with stearic acid as a flame retardant. Of aluminum hydroxide was added and mixed. This mixture is X
The components were placed in a raw material tank of a multi-component mixed foaming machine. Next, a mixture of industrial 85% phosphoric acid and phenylphosphonic acid in a molar ratio of 2: 1, and a weight ratio of 1: 0.69 was added to Y.
Ingredients were placed in separate ingredient tanks.

On the other hand, two color steel plates each having a thickness of 0.4 mm as a skin material and four aluminum frames each having a thickness of 2 mm and a height of 100 mm were assembled, and 1000 mm × 1000 mm having inlets at four corners. A 100 mm sandwich panel frame was prepared. Subsequently, the respective components X and Y were added to a mixing head of a multi-component mixing and foaming machine at a discharge weight ratio of X: Y = 100: 10.5, for a total of 3 kg / mi.
n, and the reactive composition was discharged. Incidentally, this is a ratio of the number of hydroxyl groups of phosphoric acid and phenylphosphonic acid to the number of epoxy groups of the epoxy resin is 1.0 to 1.0.
Is equivalent to 10000 g of this reactive composition was immediately injected into the above sandwich panel frame at room temperature from an injection port and foamed. Foaming started 45 seconds after injection and foam hardening was completed 5 minutes later. Thereafter, the panel was left to cool naturally to cool.

Comparative Example 1 100 parts by weight of a phenol novolak polyglycidyl ether-based epoxy resin having an epoxy equivalent of 175 g / eq and a molecular weight of about 600, 1,1-dichloro-1-as a foaming agent
15 parts by weight of fluoroethane, and 3 parts by weight of a dimethylpolysiloxane polyoxyalkylene copolymer as a foam stabilizer were put into a stirring tank equipped with a cooling tower, and thoroughly stirred and mixed.
50 parts by weight of an amino resin as an aldehyde-based condensable resin obtained by adding 2.2 mol of formaldehyde to 1 mol of melamine, and an average particle diameter of 30 μm as a flame retardant
Of aluminum hydroxide was added and mixed. This mixture was designated as X component and put in a raw material tank of a multi-component mixed foaming machine. Next, 89% phosphoric acid for industrial use was used as the Y component and placed in another raw material tank.

On the other hand, two color steel plates each having a thickness of 0.4 mm as a skin material and four aluminum frames each having a thickness of 2 mm and a height of 50 mm were assembled, and 1000 mm × 1000 mm having injection holes at four corners. A sandwich panel frame of × 50 mm was prepared. Subsequently, the respective components X and Y were fed into the mixing head of the multi-component mixed foaming machine at a flow rate of 3 Kg / min at a discharge weight ratio of X: Y = 100: 2.7. This corresponds to 0.35 in the ratio of the number of hydroxyl groups of phosphoric acid to the number of epoxy groups of the epoxy resin. 7,500 g of this reactive composition was immediately injected into the above sandwich panel frame at room temperature from an injection port and foamed. Foaming started 60 seconds after injection and ended 7 minutes later. However, the foam was insufficiently cured, and was a sandwich panel that easily deformed when a part of the skin material was pressed.

Comparative Example 2 100 parts by weight of a phenol novolak polyglycidyl ether epoxy resin having an epoxy equivalent of 175 g / eq and a molecular weight of about 600, and 1,1-dichloro-1- as a foaming agent
15 parts by weight of fluoroethane, and 3 parts by weight of a dimethylpolysiloxane polyoxyalkylene copolymer as a foam stabilizer were put into a stirring tank equipped with a cooling tower, and thoroughly stirred and mixed.
250 parts by weight of an amino resin as an aldehyde-based condensable resin obtained by adding 2.2 mol of formaldehyde to 1 mol of melamine, and an average particle diameter of 30 μm as a flame retardant
and 100 parts by weight of aluminum hydroxide. This mixture was designated as X component and put in a raw material tank of a multi-component mixed foaming machine. Next, 89% phosphoric acid for industrial use was used as the Y component and placed in another raw material tank.

On the other hand, two color steel plates each having a thickness of 0.4 mm as a skin material and four aluminum frames each having a thickness of 2 mm and a height of 50 mm were assembled, and 1000 mm × 1000 mm having injection holes at four corners. A sandwich panel frame of × 50 mm was prepared. Subsequently, the respective components X and Y were fed into the mixing head of the multi-component mixing and foaming machine at a total flow rate of 3 kg / min at a discharge weight ratio of X: Y = 100: 3.6. This corresponds to 0.8 in the ratio of the number of hydroxyl groups of phosphoric acid to the number of epoxy groups of the epoxy resin. 7,500 g of this reactive composition was immediately injected into the above sandwich panel frame at room temperature from an injection port and foamed. Foaming started 60 seconds after the injection, and once foamed to a predetermined size, the foam as the core material shrunk with time, and a sandwich panel having voids in the frame was obtained.

Comparative Example 3 100 parts by weight of a resole type phenol resin, 20 parts by weight of 1,1-dichloro-1-fluoroethane as a foaming agent,
And 2 parts by weight of polyoxyethylene sorbitan monostearate as a foam stabilizer was put into a stirring tank equipped with a cooling tower and mixed well, and then the average particle diameter as a flame retardant was 30 μm.
Of aluminum hydroxide was added and mixed. This mixture was designated as X component and put in a raw material tank of a multi-component mixed foaming machine. Next, a 60% aqueous solution of phenylphosphonic acid was charged into another raw material tank as a Y component.

On the other hand, two color steel plates each having a thickness of 0.4 mm as a skin material and four aluminum frames each having a thickness of 2 mm and a height of 50 mm were assembled, and 1000 mm × 1000 mm having injection holes provided at four corners. A sandwich panel frame of × 50 mm was prepared. Subsequently, each of the X and Y components was fed into the mixing head of the multi-component mixing and foaming machine at a discharge flow ratio of X: Y = 100: 15 at a total flow rate of 3 kg / min. 7,500 g of this mixture was immediately injected into the above sandwich panel frame at room temperature from the injection port, and heated to 60 ° C. to foam. Foaming started 3 minutes and 30 seconds after heating, and foaming hardening was completed 10 minutes later. However, the obtained sandwich panel, during the fire resistance test, the skin material on the flame side and the core material peeled off, and the back surface temperature sharply rises at the boundary, which is the upper limit of the back surface temperature in the fire resistance test 260 It was rejected over ℃. Further, when the panel was disassembled after the fire resistance test, cracks were observed in the portion of the core material peeled off from the skin material.

Comparative Example 4 A sandwich panel was obtained in the same manner as in Comparative Example 3, except that the amount of the mixture to be injected into the sandwich panel frame from the multi-component foaming machine was 10,000 g.

Examples 1 to 4 and Comparative Examples 1, 3, and 4
The sandwich panel obtained in the above was evaluated for its thickness, core material density, heat conductivity of the core material, and fire resistance. Table 1 shows the results. In addition, the density and thermal conductivity of the core material are based on a method according to JIS A 9511, and
The fire resistance of the panel was evaluated according to JIS A 1304.

[0102]

[Table 1]

[0103]

As shown in the above embodiments, the fire-resistant insulation panel of the present invention can easily and quickly foam and harden an epoxy resin foam used as a core material at room temperature without using an adhesive. Since the material can be bonded to the skin material, the production is simple and the productivity is good.

The epoxy resin foam used as the core material of the fire-resistant heat-insulating panel of the present invention has phosphoric acid and the like incorporated in the resin skeleton constituting the foam, and has an aldehyde-based condensation property with the epoxy resin. It is a combination of a resin and a combination of a flame retardant and phosphoric acid, so that the wettability between the epoxy resin and the flame retardant is improved.
There is no breakage of the cells of the foam due to the flame retardant, and since the flame retardant releases dehydration or water of crystallization by heating, the heat-insulating fireproof panel using this foam as the core material has excellent heat insulation and fire resistance. .

────────────────────────────────────────────────── ─── Continuation of the front page (56) References JP-A-11-13166 (JP, A) JP-A-8-82021 (JP, A) (58) Fields investigated (Int. Cl. ⁷ , DB name) E04B 1/74-1/98 B32B 1/00-35/00

Claims (7)

(57) [Claims] 1. A fire-resistant and heat-insulating panel in which a core material made of a resin foam is covered with a skin material, wherein the resin foam has an epoxy resin having two or more epoxy groups in a molecule, and a phosphoric acid. A composition comprising at least one phosphoric acid selected from polyphosphoric acid and phenylphosphonic acid, a foaming agent, and a foam stabilizer; a ratio of the number of hydroxyl groups of the phosphoric acid to the number of epoxy groups of the epoxy resin. Is 0.4
A resin skeleton which is reacted at a usage amount of ~ 1.0, and further comprises 5-200 parts by weight of an aldehyde-based condensable resin based on 100 parts by weight of the epoxy resin, a metal hydroxide and a metal oxide. A fire-resistant and heat-insulating panel comprising: at least one flame retardant selected from hydrates; 10 to 300 parts by weight based on 100 parts by weight of the epoxy resin. 2. A fire-resistant and heat-insulating panel in which a core material made of a resin foam is covered with a skin material, wherein the resin foam has an epoxy resin having two or more epoxy groups in a molecule, and a phosphoric acid. A mixture of at least one phosphoric acid selected from polyphosphoric acid and phenylphosphonic acid, and at least one phosphoric acid compound selected from phosphate and phosphate having a hydroxyl group bonded to a phosphorus atom;
A composition comprising a foaming agent and a foam stabilizer is used in an amount such that the ratio of the total number of hydroxyl groups of the phosphoric acids and the phosphoric acid compound to the number of epoxy groups of the epoxy resin is 0.4 to 1.0. Having a resin skeleton obtained by the reaction, and further comprising 5 to 200 parts by weight of the aldehyde-based condensable resin based on 100 parts by weight of the epoxy resin, and at least one selected from metal hydroxides and metal oxide hydrates. A fire-resistant and heat-insulating panel, comprising one kind of flame retardant in an amount of 10 to 300 parts by weight based on 100 parts by weight of the epoxy resin. 3. The fire-resistant and heat-insulating panel according to claim 1, wherein the epoxy resin is at least one selected from a glycidyl ether epoxy resin, a glycidyl ester epoxy resin and a cycloaliphatic epoxy resin. 4. The fire-resistant and heat-insulating panel according to claim 1, wherein the aldehyde-based condensable resin is in a solid or powder form. 5. The flame retardant has an average particle size of 1 to 300.
The fire-resistant and heat-insulating panel according to claim 1, wherein the panel has a thickness of μm. 6. The method according to claim 1, wherein the foaming agent is used in an amount of 1 to 50 parts by weight based on 100 parts by weight of the epoxy resin.
A fire-resistant insulation panel according to claim 1. 7. The method according to claim 1, wherein the foam stabilizer is used in an amount of 0.01 to 10 parts by weight based on 100 parts by weight of the epoxy resin.
Or the fire-resistant insulation panel according to 2.