JP2008074943A - Combustion-stopping composition, combustion-stopping prepreg and incombustible decorative laminated sheet - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a combustion-stopping composition, a combustion-stopping prepreg, and an incombustible decorative laminated sheet. <P>SOLUTION: The combustion-stopping prepreg is produced by compounding a thermosetting resin as an organic resin component of a binder component, a silane coupling agent, an inorganic phosphoric acid ammonium salt or an inorganic phosphoric acid metal compound and a layered inorganic material, impregnating slurry composed of the organic resin as the binder component and a water-free inorganic material to a fiber sheet, drying the impregnation product, impregnating or applying the above composition to the dried prepreg and drying the product. A core layer composed of a prepreg obtained by impregnating a fiber sheet with slurry composed of an organic resin as a binder component and a water-free inorganic material and drying the product is laminated to a decorative layer interposing a combustion-stopping sheet and the laminate is hot-pressed. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

  The present invention relates to a flameproofing composition, a prepreg for flameproofing, and an incombustible decorative board.

  Conventional brominated flame retardants and halogenated flame retardants used as flame retardants have a large amount of smoke generated during combustion, causing problems such as generation of toxic gases during combustion and the cause of metal corrosion. Therefore, a flame retardant composition combining a phosphorus-based flame retardant and a nitrogen-containing resin has been studied. For example, as a method for making a synthetic resin flame retardant, a technique of blending a phosphoric flame retardant, particularly, an ammonium polyphosphate that is particularly inexpensive and has high flame retardancy is widely known.

On the other hand, a decorative board having functions such as fire prevention and noncombustibility has been known so far, and a resin-impregnated decorative paper in which a decorative liquid for a decorative board is impregnated with a resin liquid mainly composed of a thermosetting resin. And inorganic fiber nonwoven fabric with phenol resin or melamine resin as binder component, prepreg impregnated with slurry containing metal hydroxide such as aluminum hydroxide or magnesium hydroxide is used as core layer, both are laminated and hot pressed It was.
JP 2005-264052 JP 2005-264053 A

  However, if an attempt is made to impregnate a fiber sheet with a conventional flame retardant, a large amount of the active ingredient penetrates into the fiber sheet, and the flame retardant effect cannot be fully exhibited by the heat from the surface. It was not suitable as.

  On the other hand, the prepreg used in the core layer for the nonflammable decorative board has a limit in the amount of the organic resin component as a binder component for the purpose of ensuring nonflammability, and if the organic resin content is large, the nonflammability is poor. When the amount of the organic resin is small, adhesion between the prepregs is poor, and since there is a large amount of inorganic filler on the surface of the prepreg, delamination occurs, heat resistance is greatly reduced, and puncture may occur.

  In addition, metal hydroxides such as aluminum hydroxide and magnesium hydroxide impart incombustibility due to the endothermic action when releasing crystal water, but since the incombustible effect is small with a small amount of compounding, it can be used as an organic resin component. Compared to this, a large amount must be blended, resulting in inferior machinability and workability, such as a decrease in the adhesion of the core layer and damage to the blade.

The present invention has been studied in view of such circumstances, and a fiber sheet is impregnated with a slurry composed of an organic resin as a binder component and a non-hydrous inorganic substance, and dried, and further, an organic resin component as a binder component, and A flame retardant prepreg impregnated or coated with a flame retardant composition comprising an inorganic phosphoric acid ammonium salt or a metal compound of inorganic phosphoric acid, a layered inorganic material, and a silane coupling agent. Is arranged at least directly below the resin-impregnated decorative paper.
As a result, it has nonflammability, excellent strength, small dimensional change, and further increases the organic resin content contained in the prepreg used for the core layer to such an extent that delamination does not occur. It is intended to improve.

  The flame retardant prepreg of the present invention is an inorganic fiber sheet because an active ingredient such as an ammonium salt of inorganic phosphate or a metal compound of inorganic phosphate in the flame retardant composition is inserted between layers of the layered inorganic substance. It does not penetrate to the inside, exists on the surface, forms a strong non-combustible heat insulating layer, and flame resistance is remarkably improved. Moreover, heat resistance improves by mix | blending a silane coupling agent as Table 3 and 4 of an evaluation result show. Further, since no metal hydroxide is used for the filler, the finished product has good cutting properties and does not damage the blade. Further, since a non-halogen flame retardant is used, no harmful and toxic gas or smoke is generated, and the molding machine is not corroded. Hereinafter, the present invention will be described in detail.

The base material of the core layer used in the present invention is a woven or non-woven fabric of inorganic fibers, and examples of the inorganic fibers include glass fibers, rock wool, carbon fibers, and the basis weight of the base material is 10 to 200 g / The range of m ² is suitable, and it is particularly preferable to use glass fibers that have excellent slurry impregnation properties.

  The slurry impregnated in the base material is a slurry containing only an organic resin and calcium carbonate as a filler, and the organic resin is a product in which a thermosetting resin such as amino-formaldehyde resin or phenol-formaldehyde resin is finished. An amino-formaldehyde resin that can be suitably used because it is excellent in various physical properties such as heat resistance and dimensional change, and is particularly excellent in heat resistance.

  The amino-formaldehyde resin is obtained by reacting an amino compound such as melamine, urea, benzoguanamine, acetoguanamine and formaldehyde.

  Phenol-formaldehyde resin is composed of 1 to 3 moles of formaldehyde with respect to 1 mole of phenolic hydroxyl groups of phenols such as phenol, cresol, xylenol, octylphenol, phenylphenol, bisphenol A, bisphenol S, and bisphenol F. It can be obtained by reacting under a basic catalyst such as sodium oxide or triethylamine.

  There is no restriction | limiting in particular as calcium carbonate, Heavy calcium carbonate, light calcium carbonate (precipitation calcium carbonate), etc. can be used. Heavy calcium carbonate having an average particle size of 0.05 to 10 μm, more preferably 1 to 5 μm is preferable. If the lower limit is not reached, secondary aggregation tends to occur and agglomeration tends to occur, and impregnation suitability tends to deteriorate. The surface of the decorative resin decorative board is not smooth, resulting in poor appearance. Light calcium carbonate refers to calcium carbonate that is chemically produced by firing limestone, and heavy calcium carbonate refers to finely powdered calcium carbonate prepared by dry or wet pulverization of white crystalline limestone.

  The blending ratio of the organic resin component and calcium carbonate is preferably 1: 5 to 15 in terms of solid content. If the calcium carbonate is less than the lower limit, the warp of the decorative plate is large, and if the upper limit is exceeded, the water resistance of the decorative plate is increased. Strength will fall. More preferably, a plurality of types having different average particle sizes are preferably used for closest packing, for example, those having an average particle size of 1-2 μm and those having an average particle size of 4-5 μm are 80-50: 20- When used at a ratio of 50, the filling rate is improved, the core layer becomes strong, and the moisture-proof performance is improved. Other than this blending ratio, aggregation occurs between the calcium carbonate particles, and the impregnation property to the inorganic fiber base material is lowered.

  The impregnation rate of the slurry to the base material is preferably 500 to 3000% by the calculation method represented by the formula 1, and when the impregnation rate exceeds the upper limit, the solid content drops off and is difficult to handle, and if the lower limit is not reached Delamination easily occurs.

The content of the organic resin component in the prepreg is preferably 3 to 50% according to the calculation method shown in Formula 2, and if it does not reach the lower limit, the heat resistance deteriorates, and if it exceeds the upper limit, the strength and adhesion are inferior. It becomes easy.

  In addition, a silane coupling agent is blended in the slurry to improve adhesion to the resin-impregnated decorative paper described later, and reacts with the methylol group of the amino-formaldehyde resin, the hydroxyl group of the phenol-formaldehyde resin, and the glass fiber. It is firmly bonded in three dimensions. The blending ratio of the organic resin component and the silane coupling agent is preferably 1: 0.02 to 0.3 in terms of solid content. If the silane coupling agent is less than the lower limit, sufficient adhesion with the surface design layer is achieved. If it exceeds the upper limit, the viscosity is remarkably increased and impregnation becomes difficult.

  Among the silane coupling agents, epoxy silane coupling agents are particularly preferable from the viewpoint of adhesion. For example, β- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, γ-glycidyloxypropyltrimethoxysilane, γ- Examples thereof include glycidyloxypropylmethyldiethoxysilane and glycidoxypropyltrimethoxysilane.

  The prepreg for flame retardancy of the present invention contains an organic resin component as a binder component, an inorganic phosphate compound, a layered inorganic substance, and a silane coupling agent in a prepreg obtained by impregnating and drying the slurry. It is impregnated or coated with a flameproofing composition and dried, and expands by heating to form a heat insulating layer during combustion, thereby inhibiting combustion.

  The impregnation or coating amount of the flame retardant composition is preferably 30 to 400 parts by weight based on 100 parts by weight of the organic resin component in the slurry in the prepreg obtained by drying, If it is less than the lower limit, sufficient non-combustible heat insulating effect cannot be obtained, and non-combustible performance cannot be obtained. When the upper limit is exceeded, the impregnation property and the coating property are deteriorated. Moreover, water resistance and heat resistance are also lowered.

  As the organic resin as the binder component, the aforementioned amino-formaldehyde resin or phenol-formaldehyde resin is used. The binder component is preferably 50 to 300 parts by weight with respect to 100 parts by weight of the inorganic phosphate compound, and the silane coupling agent is preferably 0.5 to 10 parts by weight with respect to 100 parts by weight of the inorganic phosphate compound. If the agent is less than the lower limit, the adhesion to the core layer, the resin-impregnated decorative paper and the flame retardant composition is likely to be inferior, and the heat resistance is also lowered.

  The inorganic phosphate compound blended in the slurry is decarburized by phosphorus when it receives heat from combustion and becomes a carbonized layer. Ammonium salt of inorganic phosphate or metal salt of inorganic phosphate is used. .

  The ammonium salt of inorganic phosphoric acid generates condensed phosphoric acid by deammonification when the decomposition temperature is reached by heating. This condensed phosphoric acid acts as a dehydration catalyst for organic matter and carbonizes the organic matter. As a result, a carbonized layer is formed, and the ammonia gas generated at this time acts as a foaming agent and has a function of expanding the resin composition. Specific examples include monoammonium phosphate, diammonium phosphate, triammonium phosphate, ammonium phosphite, ammonium hypophosphite, and ammonium polyphosphate.

  The metal salt of inorganic phosphoric acid reacts with the generated self-condensed water in the heating environment to generate gas, and also acts as a dehydration catalyst, and forms a nonflammable inorganic phosphoric acid coating itself. For example, aluminum phosphite is preferable because it has foamability.

  Layered silicate or layered graphite is used as the layered inorganic material, but as the layered silicate, for example, montmorillonite, saponite, hectorite, beidellite, stevensite, nontronite and other smectite clay minerals, vermiculite, halloysite, Swelling mica etc. are mentioned and 2 or more types may be used together. Laminar graphite is a natural graphite, scaly graphite washed with strong acid, sintered in alkali at high temperature, pretreated with oxidizing agents such as nitric acid and potassium permanganate, sulfide type, nitrogen type, organic acid The one in which the chemical of the system is inserted is used. These layered inorganic materials expand by heating and hold inorganic ammonium phosphate, inorganic metal phosphate or amino-formaldehyde resin between the crystal layers, making the carbonized layer stronger and heat insulating. It is thought that the effect improves and a synergistic effect appears.

  The layered inorganic material is preferably added in an amount of 0.05 to 20 parts by weight with respect to 100 parts by weight of the inorganic phosphoric acid compound. If the lower limit is not reached, sufficient heat insulation effect cannot be obtained, and incombustible performance cannot be obtained. . If the upper limit is exceeded, the slurry aggregates, the slurry is remarkably thickened, and impregnation and coating properties are reduced.

  Each component of the organic resin component, inorganic phosphate compound, and layered inorganic substance prevents the penetration into the prepreg and is present on the sheet surface, so that a scaly inorganic substance is blended to improve the flame-retardant effect. Is more preferable. Examples of the scale-like inorganic substance include mica such as muscovite, phlogopite, synthetic mica, metal oxide-coated mica, talc, kaolin, bentonite, sepiolite, graphite, glass flake, plate-like iron oxide pigment, metal powder, etc. Examples of the metal powder include iron oxide and aluminum powder.

  The scale-like inorganic substance has an average flake diameter of 100 μm or less, preferably 50 μm or less, and has a weight average aspect ratio (average flake diameter / average thickness) of 10 or more, preferably 20 or more. That's fine. The amount of the scale-like inorganic substance is desirably 25 to 500 parts by weight with respect to 100 parts by weight of the inorganic phosphate compound, and is tough when the ratio of the scale-like inorganic substance is less than the lower limit. A foam layer cannot be obtained. On the other hand, if the upper limit is exceeded, the slurry will remarkably thicken, so applicability will be significantly reduced. Moreover, foaming is suppressed and adhesiveness is inferior.

  A carbonized layer forming agent is blended as a component for forming a carbonized layer, and the carbonized layer forming agent is composed of carbon, oxygen, hydrogen, such as polyhydric alcohol, water-soluble polysaccharides, phenols, and expandable graphite. Can be used. The blending amount of the carbonized layer forming agent is desirably 3 to 70 parts by weight with respect to 100 parts by weight of the inorganic phosphate compound. When the ratio of the scale-like inorganic substance is less than the lower limit, tough foaming No layer is obtained. On the other hand, if the upper limit is exceeded, the slurry will remarkably thicken, so workability will be significantly reduced. Moreover, foaming is suppressed and adhesiveness is inferior.

  Examples of the polyhydric alcohol include monopentaerythritol, dipentaerythritol, tripentaerythritol, polypentaerythritol, tris (2-hydroxyethyl) isocyanate, triethylene glycol, sorbitol, resorcinol, glycerin, trimethylol methane, trimethylol propane. , Diethylene glycol, propylene glycol, hexamethylene glycol, inositol and the like.

  The water-soluble polysaccharide refers to one that dissolves at 1% by weight or more at room temperature, acts as a gelling agent, exhibits high gas barrier properties after gelation, and blocks the combustible gas of the core layer made of prepreg. Specific examples include starch, cellulose, dextrin or derivatives thereof. In particular, cellulose and dextrin are easily modified chemically, and are adjusted to have a hydrophilic structure portion and a hydrophobic structure portion in the molecule. It is easy to use suitably. It can also serve as a binder for coating impregnation, and is 5 to 60 parts by weight, preferably 10 to 50 parts by weight. Examples of cellulose or a derivative thereof include hydrated cellulose, carboxymethyl cellulose or a sodium derivative thereof, cellulose ester, cellulose ether, and the like, and cellulose ether is particularly preferable.

  Cellulose ether is a compound in which all or part of hydrogen atoms of three hydroxyl groups of monosaccharide units constituting cellulose are substituted with alkyl groups (including substituted alkyl groups). Specifically, methyl cellulose (MC), ethyl cellulose (EC), carboxymethyl cellulose (CMC), hydroxyethyl cellulose (HEC), hydroxypropyl cellulose (HPC), diethylaminoethyl cellulose, 1,3-dihydroxypropyl cellulose, and substituted with two or more types of alkyl groups Examples of mixed ethers of cellulose include carboxymethyl hydroxyethyl cellulose, hydroxyethyl methyl cellulose (HEMC), hydroxypropyl methyl cellulose (HPMC), and hydroxybutyl methyl cellulose. Loin (HBMC), include ethyl hydroxyethyl cellulose (EHEC) and 2-hydroxyethyl-1-hydroxyethyl cellulose.

The incombustible decorative board of the present invention comprises a laminate of a plurality of prepregs obtained by impregnating a slurry into a substrate and drying, a resin-impregnated decorative paper as a decorative layer, and, if necessary, a resin-impregnated surface paper, The flame retardant prepreg is disposed immediately below the decorative layer, and is obtained by hot pressing with a flat plate press, a continuous press or the like. The hot pressure conditions may be a temperature of 120 to 140 ° C. and a pressure of 40 to 70 kgf / cm ² .

The resin-impregnated decorative paper is obtained by impregnating a decorative liquid for decorative board of 80 to 160 g / m ^{2 with} a resin liquid composed of a thermosetting resin and drying it. As the thermosetting resin, the amino-formaldehyde described above is used. Resins are preferably used because of their excellent heat resistance and wear resistance.

The resin-impregnated surface paper is used for the purpose of improving the abrasion resistance when printing paper is used as decorative paper, and is made of a thermosetting resin on the surface paper that becomes transparent after impregnation of 20 to 40 g / m ^2. As the thermosetting resin, an amino-formaldehyde resin is preferably used as in the case of decorative paper.

  EXAMPLES Hereinafter, although an Example is given and demonstrated in detail, this invention is shown more concretely and is not specifically limited. In addition, the part in an Example and a comparative example shows solid content.

Core layer 100 g / m ² of glass fiber nonwoven fabric, 12 parts of phenol-formaldehyde resin, 60 parts of calcium carbonate with an average particle diameter of 2 μm, 27.5 parts of calcium carbonate with an average particle diameter of 5 μm, glycidoxypropyltrimethoxy A slurry containing 0.5 part of silane (SH-6040: manufactured by Toray Dow Corning Co., Ltd.) was impregnated so that the impregnation ratio shown in Formula 1 was 1000% to obtain a prepreg. In this case, the weight of the solid content after impregnation with the slurry is 1100 g / m ² from Equation ¹ , and the slurry content is 1000 g / m ² by subtracting the weight of the glass fiber nonwoven fabric from 1100 g / m ² .

Furthermore, 1000 g / m ² includes 12 parts of phenol resin, 87.5 parts of calcium carbonate, and 0.5 part of silane coupling agent, so that the organic resin component is 120 g / m ² and calcium carbonate is 875 g / m ^2. It is.

Therefore, the content (%) of the organic resin component in the prepreg calculated from Equation 2 is 11.0% by 120 / (100 + 120 + 875) × 100.
Flame Retardant Prepreg The flame retardant composition shown in Table 1 was applied to the surface of the prepreg so that the coating amount was 80 g / m ² and dried to obtain a flame retardant sheet.

Decorative layer A plain paper decorative paper having a basis weight of 120 g / m ² was impregnated with a melamine-formaldehyde resin so that the impregnation ratio represented by the formula 1 was 100% to obtain a melamine resin-impregnated decorative paper.

Non-combustible decorative board In order from the bottom, 1 sheet of melamine resin impregnated decorative paper, 3 sheets of prepreg, 1 sheet of flame retardant prepreg, 1 sheet of melamine resin impregnated decorative paper, 140 ° C using a flat finish plate , 100 kg / cm ² , and hot pressing under the condition of 90 minutes, to obtain a non-combustible decorative board of Example 1.

  The flame retardant composition shown in Table 1 was applied and dried in the same manner as in Example 1.

  The flame retardant composition shown in Table 1 was applied and dried in the same manner as in Example 1.

  The flame retardant composition shown in Table 1 was applied and dried in the same manner as in Example 1.

Comparative Example 1 (when the silane coupling agent is 0)
The composition shown in Table 1 was applied and dried in the same manner as in Example 1.

Comparative Example 2 (when the silane coupling agent is less than the lower limit)
The composition shown in Table 1 was applied and dried in the same manner as in Example 1.

Comparative Example 3 (when the silane coupling agent exceeds the upper limit)
The composition shown in Table 1 was applied and dried in the same manner as in Example 1.

Comparative Example 4 (when the layered inorganic material is less than the lower limit)
The composition shown in Table 1 was applied and dried in the same manner as in Example 1.

Comparative Example 5 (when the layered inorganic material exceeds the upper limit)
The composition shown in Table 1 was applied and dried in the same manner as in Example 1.

Comparative Example 6 (when the binder component is less than the lower limit)
The composition shown in Table 1 was applied and dried in the same manner as in Example 1.

Comparative Example 7 (when binder component exceeds upper limit)
The composition shown in Table 1 was applied and dried in the same manner as in Example 1.

Comparative Examples 8 to 10 (when the coating amount of the flame retardant composition is changed)
Example coating amount of阻燃of composition 1 was the 80 g / ^{m 2} in an organic resin component 120 g / ^{m 2,} respectively compared Example ^{8,9,10 0g / m 2, 30g /} m 2 The same procedure was performed except that 600 g / m ^{2 was} applied.

Inorganic phosphate compound Ammonium polyphosphate (AP462, manufactured by Clariant Japan Co., Ltd.)
Inorganic material 1: Layered silicate Montmorillonite (Kunipia F, Kunimine Industry Co., Ltd.)
Inorganic matter 2: Layered graphite scaly inorganic substance Mica (A21 manufactured by Yamaguchi Mica Industry Co., Ltd.)
Organic substance 1: Carbonized layer forming agent Tripentaerythritol Organic substance 2: Organic resin binder Melamine-formaldehyde resin Organic substance 3: Organic resin binder Phenol-formaldehyde resin silane coupling agent: Glycidoxypropyltrimethoxysilane (SH-6040: Toray Dow Corning Co., Ltd.)

The evaluation results are shown in Tables 3 and 4.

  The evaluation method was as follows.

Non-flammability: Total heat generation is 8 MJ / m ² or less in a 20-minute exothermic test / evaluation method using a cone calorimeter compliant with ISO 5660, and the maximum heat generation rate exceeds 200 kW / m ² continuously for 10 seconds or more. If there is no crack, crack or the like penetrating to the back surface of the test specimen after the test

  Adhesiveness: Insert a crosscut into the decorative layer with a cutter knife until it reaches the core layer, affix the cellophane tape, peel off rapidly, ○ if there is no peeling of the decorative layer, × if there is peeling It was.

  Also, after being immersed in boiling water for 2 hours, left in a constant temperature bath at 80 ° C. for 24 hours, where there was no peeling of the decorative layer, and there was no significant crack between the core layer and the decorative layer. What was there was marked as x.

  Applicability: For the prepreg, ◯ indicates that the composition could be applied for the target application amount, and x indicates that the composition could not be controlled by agglomeration.

  Heat resistance test: A sample having no change for 10 minutes in a state of contact with a heat source at 200 ° C. was evaluated as “◯”, and a sample in which swelling or puncture was generated was evaluated as “X”.

FIG. 2 is a structural cross-sectional view of the incombustible decorative board of the present invention.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 Resin impregnated decorative paper layer 2 Prepreg 3 Core layer 5 Flameproofing prepreg 7 Noncombustible decorative board

Claims (3)

A composition for flame retarding, comprising an organic resin component as a binder component, an ammonium salt of inorganic phosphoric acid or a metal compound of inorganic phosphoric acid, a layered inorganic substance, and a silane coupling agent. The fiber sheet is impregnated with a slurry composed of an organic resin as a binder component and a non-hydrous inorganic substance and dried, and the prepreg is further impregnated with, or coated with, and dried. A prepreg for flameproofing. A non-combustible decorative board having a decorative layer formed on at least one side of a core layer, the core layer being a prepreg impregnated and dried with a slurry comprising an organic resin as a binder component and a non-hydrous inorganic substance in a fiber sheet A non-combustible decorative board, wherein the flame-retardant prepreg is disposed at least immediately below the decorative layer.

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