JP2001026406A - Amorphous powder - Google Patents

Abstract

PROBLEM TO BE SOLVED: To obtain a starting material of a material improved in bending strength without deteriorating processability and productivity by specifying the ratio of Al, Si and Ca in terms of their oxides i.e., Al2O3, SiO2 and CaO and the specific surface area of porous powder containing Al, Si and Ca. SOLUTION: Amorphous powder comprising porous inorganic amorphous bodies is formed by solid solution formation, hydration reaction or the like of an oxide containing Al, Si and Ca. This amorphous powder contains Al, Si and Ca and has 0.2-7.9 CaO/SiO2 ratio and 0.2-12.5 Cab/Al2O3 ratio in terms of oxides of Al, Si and Ca, 1.6-200 m2/g specific surface area and preferably around 1-100 μm average particle diameter. A light weight composite hardened body excellent in compressive strength and bending strength is obtained by hardening this amorphous powder using a binder without deteriorating processability and productivity. The composite hardened body is used suitably as a core material for a building material for making it lightweight.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an amorphous powder which can be used as a raw material for various industrial materials, a composite cured product using the same, and a composite building material.

[0002]

2. Description of the Related Art Effective utilization of various industrial wastes has been studied in recent years from the viewpoint of protecting the global environment. For example, in the construction industry, which has consumed a large amount of forest resources until now, new construction materials are required for industrial waste,
In addition to suppressing the consumption of forest resources, the conventional inorganic boards, for example, calcium silicate board, perlite board, slag gypsum board, wood chip cement board, gypsum board, etc., realize low cost and high functionality. Suggestions have been made for it.

For example, Japanese Patent Application Laid-Open No. 7-41350 discloses that pulp residue (scum) generated after the production of paper is effectively used as a building panel. In this technique, an inorganic substance such as silica or alumina obtained by firing a scum is mixed with cement, fiber and water, and pressed against a porous iron plate. Also, Japanese Patent Laid-Open No. 10-21
No. 8643 discloses a cement admixture containing waste molten slag.

[0004]

However, Japanese Patent Application Laid-Open No.
In the technique disclosed in Japanese Patent No. 41350, there is a problem that the workability is poor because the iron plate and the cement are used, and that the cement requires curing, so that the productivity is reduced. In addition, the fired product of the disclosed scum is crystalline because it is heated at 800 to 1000 ° C., and the cement using such a fired product has a problem that bending strength and impact resistance are poor. Become.

The technique disclosed in Japanese Patent Application Laid-Open No. 10-218643 has a specific surface area of 2000 to 15000 cm ² / g, and when such a powder having a small specific surface area is solidified with a binder, the compressive strength and bending strength are reduced. Was low. That is, in order to use industrial waste as a pillar or a plate, it is necessary to increase the bending strength.

[0006] Furthermore, since any technique uses cement, nails or the like cannot be hit, and if forcedly hit, there is a disadvantage that cracks may be generated.

Therefore, the present invention solves the above-mentioned problems and, without impairing workability and productivity, a composite cured product having particularly improved bending strength and a composite building material using the composite cured product. And an amorphous powder suitable for those raw materials.

[0008]

The gist of the present invention is as follows.
It is as follows. (1) A porous powder containing an inorganic amorphous material, having a specific surface area of 1.6 to 200 m ² / g.

(2) A porous powder containing an amorphous body composed of two or more oxides, having a specific surface area of 1.6.
An amorphous powder characterized by having a particle size of ²⁰⁰ m ² / g.

(3) A composite cured product comprising the amorphous powder described in (1) or (2) and a binder.

(4) A composite cured product comprising the amorphous powder described in (1) or (2) above, a binder and a fibrous material.

(4) The composite cured product according to (4), wherein the fibrous material is oriented. Here, that the fibrous material is oriented means that the longitudinal direction of each fiber is aligned in a specific direction.

(5) A composite building material in which a reinforcing layer is formed on at least one surface of a core material, wherein the core material has
(5) A composite building material obtained by applying the composite cured product according to any of (5).

[0014]

BEST MODE FOR CARRYING OUT THE INVENTION The amorphous powder of the present invention basically contains an amorphous material composed of two or more oxides. Here, an amorphous body composed of two or more oxides refers to an oxide (1) -oxide (2)... -Oxide (n) (where n is a natural number and (1), oxide (2),... Oxide (n) are different oxides).

Although it is difficult to accurately define such an amorphous substance, it is an amorphous compound which is formed by a solid solution or hydration reaction of two or more oxides. Conceivable. Such an amorphous compound is analyzed by X-ray fluorescence analysis to determine the elements (Al, Si, C
a, Na, Mg, P, S, K, Ti, Mn, Fe and Zn), and a halo was found in the range of 2θ: 15 ° to 40 ° in the analysis chart by X-ray diffraction. Can be seen. This halo is a gradual undulation of the intensity of the X-ray, and is observed as a broad swell on the X-ray chart. The halo has a half width of 2θ: 2 °.
That is all.

It is important that the amorphous powder containing this amorphous material is porous and has a specific surface area of 1.6 to 200 m ² / g. That is, as described later, the amorphous powder is hardened with a binder to form a composite cured body, and is provided, for example, as a core material of a building material. If the material is of high quality, the unevenness of the powder is large, so that the adhesiveness with the binder is increased. As a result, the strength of the composite cured product after solidification can be improved. Further, when the amorphous powder is porous, the bulk density of the composite cured body can be reduced, and a lightweight composite cured body, that is, a core material for building materials can be obtained. You.

In particular, the specific surface area of the amorphous powder is 1.6 to 2
Advantageously, it is 00 m ² / g. This is because, when a composite cured product is produced by solidifying amorphous powder with a binder, if the specific surface area of the powder is less than 1.6 m ² / g, the contact area between the binder and the powder is too small. This is because the compression strength and bending strength of the obtained composite cured body are reduced, and when it exceeds 200 m ² / g, the powder becomes too fine, and the compression strength and bending strength are also reduced. Therefore, by adjusting the specific surface area of the amorphous powder within the above range, a composite cured product having excellent compressive strength and bending strength can be obtained.

By hardening the above-mentioned amorphous powder with a binder, a composite hardened body 2 to which the amorphous powder 1 is bonded is obtained as shown in FIG. This composite cured body 2
Is that since the amorphous powder 1 has higher strength and toughness than the crystalline body, it becomes an effective strength-expressing substance, so that the compressive strength and the bending strength value are improved. And a homogeneous cured product can be obtained. Furthermore, since it is an amorphous body, there is an advantage that sufficient strength can be obtained at a low density, and a light composite cured body can be obtained by hardening with a binder or the like.

As shown in FIG. 2, it is possible to improve the fracture toughness value of the composite cured product 2 by further mixing a fibrous material 3 with the composite cured product 2 shown in FIG. . Here, it is preferable to use the amorphous powder 1 having an average particle diameter of 1 to 100 μm for the composite cured body 2. This is because if the average particle size is outside the above range, a composite cured product having sufficient strength and toughness cannot be obtained.

The reason why the above-mentioned amorphous material becomes a strength-expressing substance is not clear, but it is presumed that it is because the progress of cracks is inhibited as compared with the crystalline structure. Further, since the fibrous material is more easily dispersed uniformly in the amorphous state than in the crystalline state, it is considered that the fracture toughness value is also improved. As a result, even if a nail is driven or a through hole is provided,
Since cracks do not occur, it is optimal for materials that require processing, such as building materials.

Here, as the oxide, a metal and / or nonmetal oxide can be used, and Al ₂ O ₃ , SiO _{2
2, CaO, Na 2 O,} MgO, P 2 O 5, SO 3, K
It is desirable to be selected from ₂ O, TiO ₂ , MnO, Fe ₂ O ₃ and ZnO. In particular, Al ₂ O ₃ —Si
O ₂ —CaO-based or Al ₂ O ₃ —SiO ₂ —CaO—
The most suitable is an oxide-based amorphous material or a composite of these amorphous materials. The oxide in the latter amorphous body is at least one kind of metal and / or non-metal oxide except Al ₂ O ₃ , SiO ₂ and CaO.

First, the amorphous body composed of Al ₂ O ₃ —SiO ₂ —CaO system is composed of Al ₂ O ₃ , SiO ₂ and CaO.
Is a compound having an amorphous structure in which all or a part of each component is formed by solid solution or hydration reaction with each other. That is, Al ₂ O ₃ and SiO ₂ , SiO ₂ and Ca
O, Al ₂ O ₃ and CaO, and Al ₂ O ₃ , SiO ₂
It is considered to include any of the compounds formed by causing a solid solution or a hydration reaction or the like with a combination of CaO and CaO. In such an inorganic amorphous compound, Al, Si, and Ca are confirmed by fluorescent X-ray analysis, and a halo is seen in the range of 2θ: 15 ° to 40 ° in an analysis chart by X-ray diffraction.

Also, Al ₂ O ₃ , SiO ₂ and CaO
Other than at least one oxide, ie, Al
_The amorphous body composed of ₂ O ₃ —SiO ₂ —CaO—oxide system includes, in addition to the combination of the above Al ₂ O ₃ —SiO ₂ —CaO system, Al ₂ O ₃ and oxide, and SiO ₂ and oxide , C
aO and oxide, Al ₂ O ₃ and SiO ₂ and oxide, SiO
₂ and CaO and an oxide, Al ₂ O ₃ and CaO and an oxide, or a compound formed by performing a solid solution or hydration reaction with a combination of Al ₂ O ₃ and SiO ₂ and CaO and an oxide. It is considered to include.

Incidentally, the number of the oxides is two or more, that is, Al
₂ O ₃ —SiO ₂ —CaO—oxide (1)... Oxide (n), if it is an amorphous substance (n is a natural number of 2 or more), these oxides, for example, oxide ( 1), oxide (2) ... oxide (n) (n is a natural number of 2 or more, and oxide (n) means different oxides if the value of n is different, and Al ₂ O ₃ , excluding SiO ₂ and CaO).
A compound produced by performing a solid solution or hydration reaction or the like in a combination of species, a compound produced by performing a solid solution or hydration reaction in at least two kinds of combinations selected from Al ₂ O ₃ , SiO ₂ and CaO, Further, at least one selected from oxides (1), oxides (2)... Oxides (n) (n is a natural number of 2 or more),
It is considered to include any of the compounds formed by solid solution or hydration reaction in combination with at least one selected from Al ₂ O ₃ , SiO ₂ and CaO.

Such an inorganic amorphous compound has a fluorescent X
According to the line analysis, in addition to Al, Si and Ca, the elements (Na, Mg, P, S, K, Ti, Mn, F
e, at least one selected from Zn) is confirmed. According to the analysis chart by X-ray diffraction, 2θ: 15 ° to
Halos can be seen in the range of 40 °.

Here, Al ₂ O ₃ , SiO ₂ and Ca
Oxides to be combined with O are one kind or two or more kinds, and are metals other than Al ₂ O ₃ , SiO ₂ and CaO and / or
Alternatively, non-metal oxides can be used, such as Na ₂ O, M
gO, P ₂ O ₅ , SO ₃ , K ₂ O, TiO ₂ , MnO,
It can be selected from Fe ₂ O ₃ and ZnO. This selection can be made based on the characteristics expected of the composite cured product.

For example, since Na ₂ O or K ₂ O can be removed with an alkali or the like, if the removal treatment is performed prior to the plating treatment, the surface to be plated on the surface of the composite hardened body becomes rough and acts as an anchor for plating. be able to. Mg
O forms a solid solution with Al ₂ O ₃ , SiO ₂ , and CaO to contribute to strength development, and greatly improves bending strength and impact resistance. P
₂ O ₅ is particularly advantageous when used for biomaterials (artificial roots, artificial bones) to aid adhesion with bone. SO ₃
Has a bactericidal action and is suitable for antibacterial building materials. TiO
₂ is a white colorant and also acts as a photo-oxidation catalyst, so it can forcibly oxidize attached organic pollutants and can be cleaned only by irradiating light. Has a unique effect that it can be used as a reaction catalyst. MnO is useful as a dark colorant, Fe ₂ O ₃ is useful as a light colorant, and ZnO is useful as a white colorant. In addition, these oxides
Each may exist alone in the amorphous body.

The composition of the above-mentioned amorphous material is Al ₂ O
₃ , in terms of SiO ₂ and CaO, Al ₂ O ₃ : 5 to 51% by weight based on the total weight of the amorphous powder, SiO ₂ :
8 to 53% by weight based on the total weight of the amorphous powder and Ca
O: 10 to 63% by weight based on the total weight of the amorphous powder,
And it is preferable to contain them in a range where the total does not exceed 100% by weight.

The reason is that the content of Al ₂ O ₃ is 5% by weight.
Less than or exceeds 51 wt%, strength of the composite cured product formed by using the amorphous powder is reduced and also, SiO ₂
If the content is less than 8% by weight or exceeds 53% by weight, the strength of the composite cured product is reduced. Further, even if the content of CaO is less than 10% by weight or exceeds 63% by weight, the strength of the composite cured product also decreases.

Further, in terms of oxide, CaO / SiO
Adjusting the ratio of ₂ to 0.2 to 7.9 and the ratio of CaO / Al ₂ O ₃ to 0.2 to 12.5 is advantageous for obtaining a composite cured body having high strength.

Further, Al ₂ O ₃ , SiO ₂ and CaO
Oxides other than Na ₂ O, MgO, P ₂ O ₅ , S
O ₃ , K ₂ O, TiO ₂ , MnO, Fe ₂ O ₃ and Z
When one or more of nO is contained, the preferred content of each component is as follows. It goes without saying that the total amount of these oxides does not exceed 100% by weight. Na ₂ O: 0.1 to 2.4% by weight based on the total weight of the amorphous powder MgO: 0.3 to 22.0% by weight based on the total weight of the amorphous powder P ₂ O ₅ : 0.1 to 14.6% by weight based on the total weight of the amorphous powder SO ₃ : 0.1 to 7.0% by weight based on the total weight of the amorphous powder K ₂ O: Amorphous 0.1 to 2.4 relative to the total weight of the Shitsukotai wt% TiO _2: 0.1 to 17.4 wt% MnO, relative to the total weight of the amorphous powder: all of the amorphous powder 0.1 to 3.0 wt% Fe ₂ O ₃ by weight: 0.2 to 35.6 wt% ZnO based on the total weight of the amorphous powder: relative to the total weight of the amorphous powder The reason for limiting the content of these oxides to the above range is that if the content deviates from the above range, the strength as a composite cured body is reduced.

It should be noted that whether or not the structure is amorphous can be confirmed by X-ray diffraction. That is, 2θ: 15 ° by X-ray diffraction
If a halo is observed in the region of ４０40 °, it can be confirmed that it has an amorphous structure. In the present invention, in addition to those having a completely amorphous structure, Hydrogen Aluminum Silicate, Kaolinite, Zeolit
e, Gehlenite, syn, Anorthite, Melitite, Gehlenit
e-synthetic, tobermorite, xonotlite, ettringite
Or SiO ₂ , Al ₂ O ₃ , CaO, Na ₂ O, Mg
O, P ₂ O ₅ , SO ₃ , K ₂ O, TiO ₂ , MnO, F
oxides such as e ₂ O ₃ and ZnO, and CaCO ₃
Crystals such as (Calcite) may be mixed. These crystals are not considered to be the strength-expressing substances themselves, but are considered to have, for example, effects such as increasing the hardness and density to improve the compressive strength and suppressing the progress of cracks. The content of the crystal is desirably 0.1 to 50% by weight based on the total weight of the amorphous powder. This is because if the number of crystals is too small, the above effect cannot be obtained, and if the number is too large, the strength is reduced.

Incidentally, the above Al ₂ O ₃ —SiO ₂ type crystalline compound is selected from the group consisting of Hydrogen Aluminum Silicate and Kaolini.
te, Zeolite, Al ₂ O ₃ —CaO based crystalline compounds are Calcium Aluminate, CaO—SiO ₂ based crystalline compounds are Calcium Silicate, Al ₂ O ₃ —SiO ₂ —Ca
O-type crystalline compounds are Gehlenite, syn and Anorthite, and Al ₂ O ₃ —SiO ₂ —CaO—MgO-type crystalline compounds are Melitite and Gehlenite-synthetic.

Further, a crystal containing Ca is desired.
Best, Gehlenite, syn (Ca_Two Al_Two O₇ ), Meliti
te-synthetic @ Ca_Two (Mg_0.5 Al_0.5 ) (Si_1.5 
Al _0.5 O₇ )｝, Gehlenite-synthetic ｛Ca_Two (M
g_0.25Al_0.75) (Si_1.25Al_0.75O₇ )｝, Anorth
ite, ordered (Ca_Two Al_Two Si_Two O₈ ), Carbonated carbon
It may contain calcium (Calcite).

In the amorphous powder of the present invention, a halogen may be added to an amorphous body composed of at least two oxides. The halogen serves as a catalyst for a solid solution or hydrate formation reaction and also acts as a combustion suppressing substance. Its content is 0.1% based on the total weight of the amorphous body.
~ 1.2% by weight is desirable. This is because if it is less than 0.1% by weight, the strength is low, and if it exceeds 1.2% by weight, harmful substances are generated by combustion. As the halogen, chlorine, bromine and fluorine are desirable.

Similarly, calcium carbonate (Calcite) may be added. Calcium carbonate itself is not a strength-expressing substance, but it is thought that by surrounding the calcium carbonate with an amorphous body, it contributes to strength improvement by actions such as inhibiting the progress of cracks. The content of calcium carbonate is desirably 48% by weight or less based on the total weight of the amorphous body. The reason for this is that if it exceeds 48% by weight, the bending strength is reduced. 0.1% by weight
The above is desirable. If the content is less than 0.1% by weight, it does not contribute to the improvement in strength.

Here, when the specific gravity of the amorphous powder is less than 2.2, the hardness and strength become low, while when it exceeds 3.0, it becomes brittle, which also leads to a decrease in strength.
It is preferably in the range of 3.0 to 3.0.

The above amorphous powders are used in various industries, for example, fillers for decorative boards, raw materials for inorganic boards, filter materials, column packing materials for chromatography, catalyst carriers, artificial bone materials, artificial limb materials. It can be applied to a resin filler for sealing electronic parts, a filler for a resist composition, and the like.

As the amorphous powder, a powder obtained by firing industrial waste is recommended, and a powder obtained by firing paper sludge (scum) is most preferable. That is,
Papermaking sludge is a pulp residue containing an inorganic substance, which is low in cost because industrial waste is used as a raw material, and contributes to solving environmental problems.

This papermaking sludge has a temperature of 300.degree.
It is desirable to fire at a temperature lower than ℃. That is, 800 ° C
This is because the above tends to be crystalline, and if the temperature is lower than 300 ° C., the pulp is only carbonized and powder cannot be obtained. Also,
An amorphous structure can also be obtained by firing papermaking sludge at 300 to 1500 ° C and then quenching.

Further, in order to make the amorphous powder porous and have a specific surface area of 1.6 to 200 m ² / g, it is desirable to treat the surface with an alkaline aqueous solution or the like.

In the papermaking sludge, in addition to pulp, Al, Si, Ca, Na, Mg, P, S, K, T
An oxide, a hydroxide or a precursor thereof, such as i, Mn, Fe and Zn, or a sol thereof, or a composite thereof, at least one selected from halogen and calcium carbonate, and water. , In general. In particular, waste paper of high quality paper contains a large amount of calcium-based crystals such as kaolin and calcium carbonate. Therefore, paper sludge containing a large amount of waste paper is suitable.

The water content in the papermaking sludge is from 20 to
Desirably, it is 80% by weight. This is because if the water content is less than 20% by weight, it becomes too hard and molding becomes difficult, while if it exceeds 80% by weight, it becomes a slurry and molding becomes difficult.

By the way, various techniques using papermaking sludge can be found, but all of them have different technical contents from the present invention. That is, JP-A-49-86438 discloses that
A hot-pressed mixture of pulp scum (cellulose component) and lime scum is disclosed, but pulp scum means cellulose and uses the inorganic component in papermaking sludge as in the present invention. However, it is not a dispersion of fibers in inorganic amorphous. For this reason, fracture at the grain boundaries of limescale or crack propagation cannot be prevented, and problems remain in bending strength and compressive strength. Moreover, the limescale is
Crystalline substance (calcium oxide) burned from paper pulp
Which is clearly distinguished from the amorphous body of the present invention.

Also, JP-A-7-47537 and JP-A-7-6
9701, 6-293546 and 5-270
No. 872 discloses a technique of combining cement and inorganic reinforcing fibers, and JP-A-10-15923 discloses a technique of mixing pulp sludge with crystalline gypsum.
Japanese Patent Application Laid-Open No. 9-2880 discloses a technique which focuses only on fibers in pulp waste, and Japanese Patent Application Laid-Open No. 53-81388 discloses a fiber in pulp waste (20% fiber, 0.01% earth and sand).
Each of the techniques described above is different from a technique in which a fibrous substance is dispersed in an inorganic amorphous material as in the present invention.

Furthermore, Japanese Patent Application Laid-Open No. 51-30088 describes a technique for forming baked ash of pulp waste and a lightweight inorganic material, but does not describe calcination conditions and the like. Cannot be obtained. JP-A-8-2
No. 46400 discloses a technique in which waste paper pulp itself is used instead of papermaking sludge. JP-A-48-443
No. 49 discloses a technique in which a pulp waste containing an organic substance and an inorganic substance is mixed with a polymer emulsion or the like. The term "inorganic" refers to silicon oxide, aluminum oxide and iron oxide. And two or more metal oxides as in the present invention are different from those constituting a complex amorphous system. And, JP
JP-A-99524 discloses a ceramic (polycrystalline) base material, which is different from an amorphous base material as in the present invention.

Next, the composite cured product of the present invention will be described. As described above, the composite cured product of the present invention is characterized by adding an amorphous powder, a binder, and, if necessary, a fibrous material. The binder used here is desirably composed of one or both of a thermosetting resin and an inorganic binder. As the thermosetting resin, one or more resins selected from phenol resins, melamine resins, epoxy resins and urea resins are desirable.
As the inorganic binder, at least one selected from the group consisting of sodium silicate, silica gel and alumina sol is desirable. Furthermore, unfired papermaking sludge can be used as a binder.

The fibrous material mixed in the composite cured product may be either organic or inorganic. As the organic fibrous material, at least one selected from synthetic fibers such as vinylon, polypropylene, and polyethylene, and organic fibrous materials composed of polysaccharides can be used, and organic fibrous materials composed of polysaccharides are preferable. . This is because OH groups exist in polysaccharides, and Al ₂
This is because it is easy to bond with various compounds of O ₃ , SiO ₂ or CaO.

The polysaccharide is desirably at least one compound selected from amino sugars, uronic acids, starch, glycogen, inulin, lichenin, cellulose, chitin, chitosan, hemicellulose and pectin.
As the organic fibrous material composed of these polysaccharides, pulp, pulp grounds, and crushed waste paper such as newspapers and magazines are advantageously suited.

On the other hand, as the inorganic fibrous material, at least one selected from alumina whiskers, SiC whiskers, silica-alumina-based ceramic fibers, glass fibers, carbon fibers, and metal fibers can be used.

The content of the fibrous material is desirably 2 to 75% by weight based on the total weight of the composite cured product. The reason for this is that if the amount is less than 2% by weight, the strength of the composite cured body is reduced, and if it exceeds 75% by weight, the fire protection performance, water resistance, dimensional stability and the like may be reduced. Further, the average length of the fibrous material is desirably 10 to 3000 μm. If the average length is too short, no entanglement occurs, and if the average length is too long, voids are formed, and the strength of the inorganic cured product tends to decrease.

On the other hand, the content of the amorphous powder in the composite cured product is preferably 10 to 90% by weight based on the total weight of the composite cured product. This is because if the content of the amorphous powder is out of the above range, the desired strength cannot be obtained.

Further, in addition to the amorphous powder, an inorganic powder may be added to the composite cured product. Specifically, at least one selected from calcium carbonate, calcium hydroxide, shirasu, shirasu balloon, perlite, aluminum hydroxide, silica, alumina, talc, calcium carbonate, kaolinite and industrial waste powder can be used. In particular, as the industrial waste powder, it is desirable to use at least one type of industrial waste powder selected from calcined powder of papermaking sludge, grinding dust of glass, and crushed silica sand. This is because by using these industrial waste powders, cost reduction can be realized and furthermore, it can contribute to solving environmental problems.

The above-mentioned composite hardened materials are used in various industries and include medical materials for artificial limbs, artificial bones and artificial roots, including new building materials replacing calcium silicate plates, perlite boards, plywood, gypsum boards and the like. It can be used for electronic materials such as a core substrate of a printed wiring board and an interlayer resin insulating layer.

Next, as one application example of the composite cured product,
The composite building material will be described below. That is, FIG.
In a composite building material in which a reinforcing layer 5 is formed on at least one surface of the core material 4 and on both surfaces in the illustrated example, as shown in FIG. Features. That is, by using the core 4 as the composite cured body 2 of the present invention, even when a tensile force is applied to the core, the core itself has excellent bending strength.
In addition, the reinforcing layer is provided on the surface of the core material, so that the structure is not easily broken. Also,
Even if pressure is locally applied to the surface, no dent or depression occurs.

Further, the composite building material of the present invention is provided with a decorative layer such as a coating, a decorative plate and a decorative veneer on the reinforcing layer 5 upon its use. Scratches such as dents are less likely to occur, and the decorative surface is not distorted by the scratches and the design is not degraded.

The reinforcing layer 5 has a structure in which the fiber base material 5b is embedded in the resin 5a. It is particularly desirable to use a thermosetting resin for the resin 5a. That is, unlike a thermoplastic resin, a thermosetting resin has excellent fire resistance and does not soften even at a high temperature, so that the function as a reinforcing layer is not lost. As the thermosetting resin, a phenol resin, a melamine resin, an epoxy resin, a polyimide resin, a urea resin and the like are suitable. In order to impart sufficient rigidity, impact resistance, and even higher fire resistance to the reinforcing layer, the content of the thermosetting resin in the reinforcing layer is desirably in the range of 10% by weight to 65% by weight.

On the other hand, it is desirable to use inorganic fibers for the fiber base material 5b. This is because the strength of the reinforcing layer 5 can be improved and the coefficient of thermal expansion can be reduced. It is preferable to use glass fiber, rock wool, and ceramic fiber as the inorganic fiber because they are low in cost and have excellent heat resistance and strength. This fiber base material is a material obtained by molding a discontinuous fiber into a mat shape, or a material obtained by cutting continuous long fibers into a mat shape by cutting into 3 to 7 cm (a so-called chopped strand mat), and dispersing in water to form a sheet. A material obtained by piling up, a continuous long fiber spirally laminated to form a mat, or a continuous long fiber woven is applicable.

Further, the thickness of the reinforcing layer is from 0.2 mm to
It is desirable to be 3.5 mm. This is because, if it is set in this range, sufficient rigidity and impact resistance can be obtained, and high workability can be maintained. The reinforcing layer may contain a flame retardant such as aluminum hydroxide and magnesium hydroxide, and a commonly used inorganic binder such as silica sol, alumina sol, and water glass.

The method for producing the amorphous powder, the composite cured product and the composite building material of the present invention will be described below. First, a method for producing an amorphous powder is as follows. First, paper sludge is prepared as a raw material. This papermaking sludge includes pulp production processes for producing printing and information paper, kraft paper, titanium paper, tissue paper, dust paper, toilet paper, sanitary products, towel paper, industrial hybrid paper, household hybrid paper, and raw materials. It is desirable to use papermaking sludge discharged from a processing step, a papermaking step, and the like. As commercially available papermaking sludge, “raw sludge” handled by Maruto Kiln Co., Ltd. can be used.

After the papermaking sludge is dewatered, it is calcined at 300 ° C. or more and less than 800 ° C. for 30 minutes to 10 hours. Can be obtained.

Next, a method for producing a composite cured product will be described.
That is, the amorphous powder is mixed with a binder and, if necessary, a fibrous material to prepare a raw material mixture. Here, when unfired papermaking sludge is used, since the sludge contains an inorganic substance and pulp, the binder and the fibrous material can be mixed at the same time, which is advantageous. The raw material mixture is poured into a desired mold, or into a mold provided with a filter, and then pressed to remove moisture, or formed into a slurry by mixing the raw material mixture. After this molding, drying and curing are performed at a heating temperature of 20 to 160 ° C. to obtain a composite cured product. In addition, if the heating temperature is too high, deformation or cracks are generated, and if it is too low, it takes a long time for drying, and productivity is lowered, which is not preferable.

In particular, in order to form the composite cured product into a plate shape,
The papermaking sludge is formed into a sheet by a known method such as circular net forming, fourdrinier forming, dewatering press forming, extrusion forming, etc. And dried, and the sheet-shaped molded body is pressed while being heated at a heating temperature of 80 to 160 ° C.,
It is formed into a plate-shaped core material. The pressure at that time is 1 to 120 kg
f / cm ² is appropriate.

Here, the term "pressing" refers to maintaining the pressure applied. Then, the fibrous material is oriented in a direction crossing the pressing direction by the pressure applied at the time of pressing, so that the bending strength of the core material can be improved. In addition, the pressurization removes moisture and suppresses the progress of crystallization, which is advantageous for forming an amorphous body.

Further, the inorganic powder can be dispersed in the composite cured product by adding and mixing the inorganic powder to the papermaking sludge, followed by heating and curing.

In addition to the papermaking sludge, metal alkoxides and metal hydroxides can be used as raw materials. For example, a mixture of alkoxides and hydroxides of Al, Si and Ca and a crushed material obtained by crushing waste paper are mixed, and the mixture is hydrolyzed and polymerized in the presence of an acid or alkali to form a sol. May be gelled. Such gels result in Al ₂ O ₃ , SiO ₂ , Ca
O, Na ₂ O, MgO, P ₂ O ₅ , SO ₃ , K ₂ O, T
It is presumed to be the same as a compound obtained by solid solution or hydration reaction of an oxide such as iO ₂ , MnO, Fe ₂ O ₃ and ZnO.

The composite building material is manufactured as follows. First, the papermaking sludge is formed into a sheet by a known method such as circular net forming, fourdrinier forming, dewatering press forming, and extrusion forming, and dried, or while the sludge is conveyed by a conveyor, the sheet is pressed by a roll. It is a shaped body. On the other hand, the fiber base material is impregnated with a resin, heated at 25 to 70 ° C., and dried to obtain a reinforcing sheet. Next, the sheet-shaped molded body and the reinforcing sheet are laminated, and pressed while heating,
It is molded into a composite building material consisting of a core material (composite cured body) and a reinforcing layer. It is appropriate that the heating temperature here is 80 to 200 ° C. and the pressure is about 1 to ²⁰ kgf / cm ² .

Instead of the above method, a mat of inorganic fibers is impregnated with a resin composition, dried, heated and pressed, and the thermosetting resin is cured to form a reinforcing layer.
A method of attaching this reinforcing layer to a core material which has been cured in advance with an adhesive may be used. Further, a thermosetting resin, for example, at least one thermosetting resin selected from phenol resin, melamine resin, epoxy resin, urea resin and urethane resin may be applied to the surface of the core material 4.

Further, the surface of glass fiber, rock wool or ceramic fiber is coated with a thermosetting resin such as phenol resin in a different configuration, and a fiber base made of these fibers is laminated on a sheet-like molded body. And hot pressing. This method of coating the fiber surface with a thermosetting resin in a separate step is advantageous because the adhesion to the impregnated resin is improved, the fibers are easily bonded to each other, and the resin impregnation rate can be further improved. . As a method of such coating, a method of impregnating the fiber base material with an uncured thermosetting resin and drying,
Alternatively, there is a method in which a raw material melt of glass fiber, rock wool or ceramic fiber is discharged from a nozzle, fiberized by a blowing method or a centrifugal method, and a solution of a thermosetting resin such as a phenol resin is sprayed simultaneously with the fiberization. .

When glass fiber, rock wool, or ceramic fiber is used as a constituent material of the fiber base material, it is preferable to coat a silane coupling agent. The surface of the composite building material obtained in this way,
The back surface can be painted, or a decorative plate or a decorative veneer can be attached with an adhesive or the like. The coating is performed by printing and spraying various pigments, inks, and the like. The decorative board is a three-layer decorative board including a phenol resin-impregnated core layer, a melamine resin-impregnated pattern layer, and a melamine resin-impregnated overlay layer, a melamine resin-impregnated backer layer, a phenol resin-impregnated core layer, and a melamine resin-impregnated pattern layer. And a decorative plate having a four-layer structure composed of an overlay layer impregnated with a melamine resin. In particular, in the case of a decorative board having a phenolic resin-impregnated core layer as the core layer, the surface strength is significantly increased, so that it can be applied to flooring materials and the like. In addition, high quality wood such as cedar and cypress can be used as the decorative veneer.

[0071]

EXAMPLES (Example 1) Unfired papermaking sludge ("raw sludge" handled by Maruto Kiln Co., Ltd .: solid content 34% by weight, moisture 66)
% By weight) is dried at 80 ° C. while stirring,
After the obtained dried body was calcined at 780 ° C. for 5 hours, it was immediately exposed to room temperature and rapidly cooled. Further, the fired product was ball-milled for 5 hours to obtain 248 g of amorphous powder.

This amorphous powder was converted into a fluorescent X-ray analyzer (Ri
Analysis using GIX RIX2100) revealed that the composition was as follows in terms of oxide. The specific surface area was measured according to JIS R-1626 (BET method: one-point method of flow method). SiO ₂ : 34.1% by weight, Fe ₂ O ₃ : 1.6% by weight CaO: 32.1% by weight, TiO ₂ : 1.0% by weight Al ₂ O ₃ : 20.7% by weight, SO ₃ : 0.5 wt% MgO: 5.9 wt%, Cl: 0.2% by weight P ₂ O _5: 2.8 wt%, ZnO: 0.1 wt% Others: trace average particle size: 11.0 .mu.m true specific gravity : 2.756 Specific surface area: 19.0 m ² / g

Further, the crystal structure was confirmed by X-ray diffraction. FIG. 4 shows a chart of the X-ray diffraction. Note that X
The line diffraction used Rigaku MiniFlex and targeted Cu. A gentle undulation (halo) is observed around 2θ: 22 °, and a peak indicating a crystal structure is also observed, indicating that the crystal structure is mixed in the amorphous structure. From the peak, Gehlenite, syn, Melitite
-synthetic, Gehlenite-synthetic, Anorthite, orde
red has been identified. The amount of crystals present is about 2
It was 0% by weight.

Next, the thus obtained amorphous powder 24
8 parts by weight and 1512 parts by weight of unfired papermaking sludge are kneaded, and while the kneaded material is conveyed on a conveyor, 35 kg
While applying a pressure of f / cm ² , a sheet-shaped molded body having a thickness of 10 mm was obtained. This sheet-like molded body was heated at 100 ° C. to obtain a plate-shaped composite cured body.

Incidentally, the side surface of the composite cured product was examined with an optical microscope (5
(0x), the fibers were oriented in a direction perpendicular to the pressing direction.

(Example 2) The fired product obtained in Example 1 was ball-milled for 10 hours to obtain 248 g of an amorphous powder. This amorphous powder is converted into a fluorescent X-ray analyzer (Rigaku
RIX2100), the composition was as follows. SiO ₂ : 34.1% by weight, Fe ₂ O ₃ : 1.6% by weight CaO: 32.1% by weight, TiO ₂ : 1.0% by weight Al ₂ O ₃ : 20.7% by weight, SO ₃ : 0.5 wt% MgO: 5.9 wt%, Cl: 0.2% by weight P ₂ O _5: 2.8 wt%, ZnO: 0.1 wt% Others: trace average particle size: 6.6 [mu] m true specific gravity : 2.756 Specific surface area: 31.7 m ² / g

Next, the thus obtained amorphous powder 24
8 parts by weight and 1512 parts by weight of unfired papermaking sludge are kneaded, and while the kneaded material is conveyed on a conveyor, 35 kg
While applying a pressure of f / cm ² , a sheet-shaped molded body having a thickness of 10 mm was obtained. This sheet-like molded body was heated at 100 ° C. to obtain a plate-shaped composite cured body.

Example 3 The calcined product obtained in Example 1 was ball-milled for 3 hours to obtain 248 g of an amorphous powder. This amorphous powder is converted into a fluorescent X-ray analyzer (Rigaku
RIX2100), the composition was as follows. SiO ₂ : 34.0 wt%, Fe ₂ O ₃ : 12.6 wt% CaO: 32.1 wt%, TiO ₂ : 1.0 wt% Al ₂ O ₃ : 20.7 wt%, SO ₃ : 0.5 wt% MgO: 6.0 wt%, Cl: 0.2% by weight P ₂ O _5: 2.7 wt%, ZnO: 0.1 wt% Others: trace average particle size: 17.6Myuemu true specific gravity : 2.756 Specific surface area: 4.8 m ² / g

Next, the thus obtained amorphous powder 24
8 parts by weight and 1512 parts by weight of unsintered papermaking sludge are kneaded, and while the kneaded material is conveyed on a conveyor, 50 kg
While applying a pressure of f / cm ² , a sheet-shaped molded body having a thickness of 10 mm was obtained. This sheet-like molded body was heated at 100 ° C. to obtain a plate-shaped composite cured body.

Example 4 The amorphous powder obtained by ball milling in Example 1 was further ball milled for 30 hours to obtain 248 g of amorphous powder. When this amorphous powder was analyzed using an X-ray fluorescence analyzer (Rigaku RIX2100), it was converted to oxide and had the following composition. SiO ₂ : 34.0 wt%, Fe ₂ O ₃ : 12.6 wt% CaO: 32.1 wt%, TiO ₂ : 1.0 wt% Al ₂ O ₃ : 20.7 wt%, SO ₃ : 0.5 wt% MgO: 6.0 wt%, Cl: 0.2% by weight P ₂ O _5: 2.7 wt%, ZnO: 0.1 wt% Others: trace average particle size: 1.5 [mu] m true specific gravity : 2.756 Specific surface area: 139 m ² / g

Next, the thus obtained amorphous powder 24
8 parts by weight and 1512 parts by weight of unfired papermaking sludge are kneaded, and while the kneaded material is conveyed on a conveyor, 3 kgf
/ Cm ² while applying a pressure of 10 mm / cm ² to obtain a sheet-shaped molded body having a thickness of 10 mm. This sheet-like molded body was heated at 100 ° C. to obtain a plate-shaped composite cured body.

(Comparative Example 1) The amorphous powder obtained by ball milling in Example 1 was further ball milled for 48 hours to obtain 248 g of amorphous powder. When this amorphous powder was analyzed using an X-ray fluorescence analyzer (Rigaku RIX2100), it was converted to oxide and had the following composition. SiO ₂ : 34.0 wt%, Fe ₂ O ₃ : 12.6 wt% CaO: 32.1 wt%, TiO ₂ : 1.0 wt% Al ₂ O ₃ : 20.7 wt%, SO ₃ : 0.5 wt% MgO: 6.0 wt%, Cl: 0.2% by weight P ₂ O _5: 2.7 wt%, ZnO: 0.1 wt% Others: trace average particle diameter: 0.98 .mu.m true specific gravity : 2.756 Specific surface area: 213 m ² / g

Next, the thus obtained amorphous powder 24
8 parts by weight and 1512 parts by weight of unfired papermaking sludge are kneaded, and while the kneaded material is conveyed on a conveyor, 3 kgf
/ Cm ² while applying a pressure of 10 mm / cm ² to obtain a sheet-shaped molded body having a thickness of 10 mm. This sheet-like molded body was heated at 100 ° C. to obtain a plate-shaped composite cured body.

(Comparative Example 2) The fired product obtained in Example 1 was ball-milled for 10 minutes to obtain 248 g of an amorphous powder. This amorphous powder is converted into a fluorescent X-ray analyzer (Rigaku
RIX2100), the composition was as follows. SiO ₂ : 34.0 wt%, Fe ₂ O ₃ : 12.6 wt% CaO: 32.1 wt%, TiO ₂ : 1.0 wt% Al ₂ O ₃ : 20.7 wt%, SO ₃ : 0.5 wt% MgO: 6.0 wt%, Cl: 0.2% by weight P ₂ O _5: 2.7 wt%, ZnO: 0.1 wt% Others: trace average particle size: 232Myuemu true specific gravity: 2 .756 Specific surface area: 0.9 m ² / g

Next, the thus obtained amorphous powder 24
8 parts by weight and 1512 parts by weight of unfired papermaking sludge are kneaded, and while the kneaded material is conveyed on a conveyor, 3 kgf
/ Cm ² while applying a pressure of 10 mm / cm ² to obtain a sheet-shaped molded body having a thickness of 10 mm. This sheet-like molded body was heated at 100 ° C. to obtain a plate-shaped composite cured body.

(Example 5) 248 parts by weight of the amorphous powder obtained in Example 1 and 62 parts by weight of a phenol resin were kneaded, and the kneaded product was conveyed on a conveyor at 3 kgf / kg.
While applying a pressure of ² cm ² , a sheet-shaped molded product having a thickness of 10 mm was obtained. The sheet-shaped molded body was pressed at a temperature of 180 ° C. and a pressure of 28 kgf / cm ^{2 for} 20 minutes to obtain a composite cured body.

(Example 6) A sheet-like glass fiber was impregnated with a phenol resin solution containing a curing agent (45% in terms of solid content in terms of impregnation amount), and then dried at a temperature of 80 ° C for 20 minutes to obtain a reinforcing sheet. Obtained. Next, a sheet-like molded body was produced in the same manner as in Example 1. Then, the reinforcing sheet is placed on the front and back surfaces of the sheet-shaped molded body, and pressed at a temperature of 110 ° C. for 20 minutes at a pressure of 7 kgf / cm ² , and a reinforcing layer having a thickness of 1 mm and a reinforcing layer having a thickness of 10 mm are formed on both sides. A composite building material consisting of a core material was manufactured. Further, a decorative veneer of cedar board having a thickness of 0.2 mm was attached to the surface of the composite building material via a vinyl acetate adhesive.

(Comparative Example 3) A slurry was prepared by mixing 60 parts by weight of fired scum fired at 1000 ° C, 36 parts by weight of water, 100 parts by weight of cement, and 0.3 parts by weight of vinylon fiber for 3 minutes by a forced stirring mixer. The slurry was poured into a mold, pressurized at 150 to 180 kgf / cm ² , and then demolded. When X-ray diffraction measurement was performed on the powder collected from the plate-like body, Gehlenite, syn, Melitite-synth
Only etic, Gehlenite-synthetic, Anorthite, and ordered peaks were observed.

Comparative Example 4 A lime-based sewage sludge molten slag (manufactured by Osaka City Sewerage Corporation, whose main chemical component is as follows) was fired at 1500 ° C., and the fineness was 3500 cm ² / blaine in a ball mill. g, 5 parts by weight, and 95 parts by weight of ordinary Portland cement (made by Chichibu Onoda) are mixed.
_The mixed cement composition was manufactured by adjusting with natural gypsum so that the amount of ₃ became 2% by weight. This cement and sand:
The mixture was mixed at a ratio of 3 and left for 3 days. Serial SiO _2: 33.4 wt%, MgO: 2.4 wt% Al ₂ O _3: 14.2 wt%, P ₂ O _5: 7.0 wt% Fe ₂ O _3: 5.0 wt%, NaO : 0.7% by weight CaO: 33.9% by weight, K ₂ O: 0.7% by weight

The cured composites or the composite building materials obtained in the above Examples and Comparative Examples were tested for flexural strength, compressive strength, workability, and nailability. Table 1 shows the results.
Shown in The test method was such that the bending strength was JIS A69.
01, and the compressive strength was measured according to the method specified in JISA 5416, respectively. The workability is
Cutting was performed with a circular saw for woodworking, and workability was determined. Further, regarding the nailing property, a diameter of 4 mm and a length of 50 mm
The nail was hit and the depth of nail penetration and the presence or absence of cracks were examined.

[0091]

[Table 1]

[0092]

As described above, the composite cured product produced using the amorphous powder of the present invention is an inexpensive material having excellent workability and productivity, particularly having high bending strength. It can be applied advantageously in various fields, and in particular, because it is possible to drive nails, it is possible to provide a material optimal for building materials at low cost.

[Brief description of the drawings]

FIG. 1 is a schematic cross-sectional view of a composite cured product of the present invention.

FIG. 2 is a schematic cross-sectional view of a composite cured product of the present invention.

FIG. 3 is a schematic sectional view of the composite building material of the present invention.

FIG. 4 is a chart of X-ray diffraction of the amorphous powder of Example 1.

[Explanation of symbols]

 DESCRIPTION OF SYMBOLS 1 Amorphous body 2 Composite hardened body 3 Fibrous material 4 Core material 5 Reinforcement layer

────────────────────────────────────────────────── ───

[Procedure amendment]

[Submission Date] August 7, 2000 (2000.8.7)

[Procedure amendment 1]

[Document name to be amended] Statement

[Correction target item name] Full text

[Correction method] Change

[Correction contents]

[Document Name] Statement

[Title of the Invention] Amorphous powder

[Claims]

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an amorphous powder which can be used as a raw material for various industrial materials.

[0002]

2. Description of the Related Art Effective utilization of various industrial wastes has been studied in recent years from the viewpoint of protecting the global environment. For example, in the construction industry, which has consumed a large amount of forest resources until now, new construction materials are required for industrial waste,
In addition to suppressing the consumption of forest resources, the conventional inorganic boards, for example, calcium silicate board, perlite board, slag gypsum board, wood chip cement board, gypsum board, etc., realize low cost and high functionality. Suggestions have been made for it.

For example, Japanese Patent Application Laid-Open No. 7-41350 discloses that pulp residue (scum) generated after the production of paper is effectively used as a building panel. In this technique, an inorganic substance such as silica or alumina obtained by firing a scum is mixed with cement, fiber and water, and pressed against a porous iron plate. Also, Japanese Patent Laid-Open No. 10-21
No. 8643 discloses a cement admixture containing waste molten slag.

[0004]

However, Japanese Patent Application Laid-Open No.
In the technique disclosed in Japanese Patent No. 41350, there is a problem that the workability is poor because the iron plate and the cement are used, and that the cement requires curing, so that the productivity is reduced. In addition, the fired product of the disclosed scum is crystalline because it is heated at 800 to 1000 ° C., and the cement using such a fired product has a problem that bending strength and impact resistance are poor. Become.

The technique disclosed in Japanese Patent Application Laid-Open No. 10-218643 has a specific surface area of 2000 to 15000 cm ² / g, and when such a powder having a small specific surface area is solidified with a binder, the compressive strength and bending strength are reduced. Was low. That is, in order to use industrial waste as a pillar or a plate, it is necessary to increase the bending strength.

[0006] Furthermore, since any technique uses cement, nails or the like cannot be hit, and if forcedly hit, there is a disadvantage that cracks may be generated.

Therefore, the present invention can solve the above-mentioned problems and can improve the bending strength without impairing the workability and productivity, and is particularly suitable for raw materials of various industrial materials such as building materials. It is intended to provide a crystalline powder.

[0008]

That is, the present invention provides:
It comprises a porous inorganic amorphous material containing Al, Si and Ca, and has a CaO / SiO ₂ ratio of 0.2 to 7.9 and C in terms of Al ₂ O ₃ , SiO ₂ and CaO.
An amorphous powder characterized in that the ratio of aO / Al ₂ O ₃ is 0.2 to 12.5 and the specific surface area is 1.6 to 200 m ² / g.

[0009]

BEST MODE FOR CARRYING OUT THE INVENTION The amorphous powder of the present invention comprises Al,
Basically contains Si and Ca. Such an amorphous body is an amorphous compound which is difficult to define precisely, but is formed by causing a solid solution or hydration reaction of an oxide containing at least Al, Si and Ca. it is conceivable that. Such an amorphous compound has a fluorescent X
According to the line analysis, the elements constituting the oxide (at least A
l, Si and Ca) are confirmed, and a halo is observed in the range of 2θ: 15 ° to 40 ° in the analysis chart by X-ray diffraction. This halo is a gradual undulation of the intensity of the X-ray, and is observed as a broad swell on the X-ray chart. The halo has a half width of 2θ: 2 ° or more.

It is important that the amorphous powder containing the amorphous material is porous and has a specific surface area of 1.6 to 200 m ² / g. That is, as described later, the amorphous powder is hardened with a binder to form a composite cured body, and is provided, for example, as a core material of a building material. If the material is of high quality, the unevenness of the powder is large, so that the adhesiveness with the binder is increased. As a result, the strength of the composite cured product after solidification can be improved. Further, when the amorphous powder is porous, the bulk density of the composite cured body can be reduced, and a lightweight composite cured body, that is, a core material for building materials can be obtained. You.

In particular, the specific surface area of the amorphous powder is 1.6 to 2
Advantageously, it is 00 m ² / g. This is because, when a composite cured product is produced by solidifying amorphous powder with a binder, if the specific surface area of the powder is less than 1.6 m ² / g, the contact area between the binder and the powder is too small. This is because the compression strength and bending strength of the obtained composite cured body decrease, and when it exceeds 200 m ² / g, the powder becomes too fine, and the compression strength and bending strength also decrease. Therefore, by adjusting the specific surface area of the amorphous powder to the above range, a composite cured product having excellent compressive strength and bending strength can be obtained.

By hardening the above-mentioned amorphous powder with a binder, for example, as shown in FIG. 1, a composite cured body 2 to which the amorphous powder 1 is bonded can be obtained. The composite hardened body 2 has the strength and toughness of the amorphous powder 1 higher than that of the crystalline body, so that it becomes an effective strength-expressing substance. As a result, the compressive strength and the bending strength are improved. A homogeneous cured product without anisotropy can be obtained. Furthermore, since it is an amorphous body, there is an advantage that sufficient strength can be obtained at a low density, and a light composite cured body can be obtained by hardening with a binder or the like.

As shown in FIG. 2, it is possible to improve the fracture toughness value of the composite cured body 2 by further mixing the fibrous material 3 with the composite cured body 2 shown in FIG. . Here, it is preferable to use the amorphous powder 1 having an average particle diameter of 1 to 100 μm for the composite cured body 2. This is because if the average particle size is outside the above range, a composite cured product having sufficient strength and toughness cannot be obtained.

[0014] The reason why the above-mentioned amorphous material becomes a strength-expressing substance is not clear, but is presumed to be because the progress of cracks is inhibited as compared with the crystalline structure. Further, since the fibrous material is more easily dispersed uniformly in the amorphous state than in the crystalline state, it is considered that the fracture toughness value is also improved. As a result, even if a nail is driven or a through hole is provided,
Since cracks do not occur, it is optimal for materials that require processing, such as building materials.

Here, the oxide is Al_Two O_Three , S
iO_Two And CaO, metal and / or non-gold
Oxides of the genus_Two O, MgO, P_Two O_Five ,
SO _Three , K_Two O, TiO_Two , MnO, Fe_Two O_Three and
It is desirable to be selected from ZnO. In particular, Al_Two 
O_Three -SiO_Two -CaO-based or Al_Two O_Three -SiO _Two 
-CaO-oxide-based amorphous material, or these
A composite of an amorphous body is optimal. In addition, the latter amorphous body
The oxide in is Al_Two O_Three , SiO_Two And CaO
At least one of metal and / or nonmetal oxides except
is there.

First, an amorphous body composed of Al ₂ O ₃ —SiO ₂ —CaO system includes Al ₂ O ₃ , SiO ₂ and CaO.
Is a compound having an amorphous structure in which all or a part of each component is formed by solid solution or hydration reaction with each other. That is, Al ₂ O ₃ and SiO ₂ , SiO ₂ and Ca
O, Al ₂ O ₃ and CaO, and Al ₂ O ₃ , SiO ₂
It is considered to include any of the compounds formed by causing a solid solution or a hydration reaction or the like with a combination of CaO and CaO. In such an inorganic amorphous compound, Al, Si, and Ca are confirmed by fluorescent X-ray analysis, and a halo is seen in the range of 2θ: 15 ° to 40 ° in an analysis chart by X-ray diffraction.

Further, Al ₂ O ₃ , SiO ₂ and CaO
Other than at least one oxide, ie, Al
_The amorphous body composed of ₂ O ₃ —SiO ₂ —CaO—oxide system includes, in addition to the combination of the above Al ₂ O ₃ —SiO ₂ —CaO system, Al ₂ O ₃ and oxide, and SiO ₂ and oxide , C
aO and oxide, Al ₂ O ₃ and SiO ₂ and oxide, SiO
₂ and CaO and an oxide, Al ₂ O ₃ and CaO and an oxide, or a compound formed by performing a solid solution or hydration reaction with a combination of Al ₂ O ₃ and SiO ₂ and CaO and an oxide. It is considered to include.

It is to be noted that the oxide is two or more, that is, Al
₂ O ₃ —SiO ₂ —CaO—oxide (1)... Oxide (n), if it is an amorphous substance (n is a natural number of 2 or more), these oxides, for example, oxide ( 1), oxide (2) ... oxide (n) (n is a natural number of 2 or more, and oxide (n) means different oxides if the value of n is different, and Al ₂ O ₃ , excluding SiO ₂ and CaO).
A compound formed by performing a solid solution or a hydration reaction or the like in a combination of species with Al ₂ O ₃ , SiO ₂ and CaO
Compounds formed by solid solution or hydration reaction, etc. in combination with Oxide (1), Oxide (2).
..Oxide (n) (n is a natural number of 2 or more) formed by performing a solid solution or hydration reaction with a combination of at least one selected from the group consisting of Al ₂ O ₃ , SiO ₂ and CaO. It is believed to include any of the compounds.

Such an inorganic amorphous compound has a fluorescent X
According to the line analysis, in addition to Al, Si and Ca, the elements (Na, Mg, P, S, K, Ti, Mn, F
e, at least one selected from Zn) is confirmed. According to the analysis chart by X-ray diffraction, 2θ: 15 ° to
Halos can be seen in the range of 40 °.

Here, Al ₂ O ₃ , SiO ₂ and Ca
Oxides to be combined with O are one kind or two or more kinds, and are metals other than Al ₂ O ₃ , SiO ₂ and CaO and / or
Alternatively, non-metal oxides can be used, such as Na ₂ O, M
gO, P ₂ O ₅ , SO ₃ , K ₂ O, TiO ₂ , MnO,
It can be selected from Fe ₂ O ₃ and ZnO. This selection can be made based on the characteristics expected of the composite cured product.

For example, since Na ₂ O or K ₂ O can be removed with an alkali or the like, if the removal treatment is performed prior to the plating treatment, the surface to be plated on the surface of the composite hardened body becomes rough and acts as an anchor for plating. be able to. Mg
O forms a solid solution with Al ₂ O ₃ , SiO ₂ , and CaO to contribute to strength development, and greatly improves bending strength and impact resistance. P
₂ O ₅ is particularly advantageous when used for biomaterials (artificial roots, artificial bones) to aid adhesion with bone. SO ₃
Has a bactericidal action and is suitable for antibacterial building materials. TiO
₂ is a white colorant and also acts as a photo-oxidation catalyst, so it can forcibly oxidize attached organic pollutants and can be cleaned only by irradiating light. Has a unique effect that it can be used as a reaction catalyst. MnO is useful as a dark colorant, Fe ₂ O ₃ is useful as a light colorant, and ZnO is useful as a white colorant. In addition, these oxides
Each may exist alone in the amorphous body.

The composition of the amorphous body is Al ₂ O, respectively.
₃ , in terms of SiO ₂ and CaO, Al ₂ O ₃ : 5 to 51% by weight based on the total weight of the amorphous powder, SiO ₂ :
8 to 53% by weight based on the total weight of the amorphous powder and Ca
O: 10 to 63% by weight based on the total weight of the amorphous powder,
And it is preferable to contain them in a range where the total does not exceed 100% by weight.

The reason is that the content of Al ₂ O ₃ is 5% by weight.
Less than or exceeds 51 wt%, strength of the composite cured product formed by using the amorphous powder is reduced and also, SiO ₂
If the content is less than 8% by weight or exceeds 53% by weight, the strength of the composite cured product is reduced. Further, even if the content of CaO is less than 10% by weight or exceeds 63% by weight, the strength of the composite cured product also decreases.

Further, in terms of oxide, CaO / SiO
_It is important to adjust the ratio of ₂ to 0.2 to 7.9 and the ratio of CaO / Al ₂ O ₃ to 0.2 to 12.5 in order to obtain a composite cured body (material) having high strength. .

Further, Al ₂ O ₃ , SiO ₂ and CaO
Oxides other than Na ₂ O, MgO, P ₂ O ₅ , S
O ₃ , K ₂ O, TiO ₂ , MnO, Fe ₂ O ₃ and Z
When one or more of nO is contained, the preferred content of each component is as follows. It goes without saying that the total amount of these oxides does not exceed 100% by weight. Na ₂ O: 0.1 to 2.4% by weight based on the total weight of the amorphous powder MgO: 0.3 to 22.0% by weight based on the total weight of the amorphous powder P ₂ O ₅ : 0.1 to 14.6% by weight based on the total weight of the amorphous powder SO ₃ : 0.1 to 7.0% by weight based on the total weight of the amorphous powder K ₂ O: Amorphous 0.1 to 2.4 relative to the total weight of the Shitsukotai wt% TiO _2: 0.1 to 17.4 wt% MnO, relative to the total weight of the amorphous powder: all of the amorphous powder 0.1 to 3.0 wt% Fe ₂ O ₃ by weight: 0.2 to 35.6 wt% ZnO based on the total weight of the amorphous powder: relative to the total weight of the amorphous powder The reason for limiting the content of these oxides to the above range is that if the content deviates from the above range, the strength as a composite cured body is reduced.

It should be noted that the presence or absence of an amorphous structure can be confirmed by X-ray diffraction. That is, 2θ: 15 ° by X-ray diffraction
If a halo is observed in the region of ４０40 °, it can be confirmed that it has an amorphous structure. In the present invention, in addition to those having a completely amorphous structure, Hydrogen Aluminum Silicate, Kaolinite, Zeolit
e, Gehlenite, syn, Anorthite, Melitite, Gehlenit
e-synthetic, tobermorite, xonotlite, ettringite
Or SiO ₂ , Al ₂ O ₃ , CaO, Na ₂ O, Mg
O, P ₂ O ₅ , SO ₃ , K ₂ O, TiO ₂ , MnO, F
oxides such as e ₂ O ₃ and ZnO, and CaCO ₃
Crystals such as (Calcite) may be mixed. These crystals are not considered to be the strength-expressing substances themselves, but are considered to have, for example, effects such as increasing the hardness and density to improve the compressive strength and suppressing the progress of cracks. The content of the crystal is desirably 0.1 to 50% by weight based on the total weight of the amorphous powder. This is because if the number of crystals is too small, the above effect cannot be obtained, and if the number is too large, the strength is reduced.

Incidentally, the Al ₂ O ₃ —SiO ₂ based crystalline compound is selected from the group consisting of Hydrogen Aluminum Silicate and Kaolini.
te, Zeolite, Al ₂ O ₃ —CaO based crystalline compounds are Calcium Aluminate, CaO—SiO ₂ based crystalline compounds are Calcium Silicate, Al ₂ O ₃ —SiO ₂ —Ca
O-type crystalline compounds are Gehlenite, syn and Anorthite, and Al ₂ O ₃ —SiO ₂ —CaO—MgO-type crystalline compounds are Melitite and Gehlenite-synthetic.

Further, a crystal containing Ca is desired.
Best, Gehlenite, syn (Ca_Two Al_Two O₇ ), Meliti
te-synthetic @ Ca_Two (Mg_0.5 Al_0.5 ) (Si_1.5 
Al _0.5 O₇ )｝, Gehlenite-synthetic ｛Ca_Two (M
g_0.25Al_0.75) (Si_1.25Al_0.75O₇ )｝, Anorth
ite, ordered (Ca_Two Al_Two Si_Two O₈ ), Carbonated carbon
It may contain calcium (Calcite).

In the amorphous powder of the present invention, Al,
Halogen may be added to the amorphous body containing Si and Ca. The halogen serves as a catalyst for a solid solution or hydrate formation reaction and also acts as a combustion suppressing substance. Its content is desirably 0.1 to 1.2% by weight based on the total weight of the amorphous body. This is because if it is less than 0.1% by weight, the strength is low, and if it exceeds 1.2% by weight, harmful substances are generated by combustion. As the halogen, chlorine, bromine and fluorine are desirable.

Similarly, calcium carbonate (Calcite) may be added. Calcium carbonate itself is not a strength-expressing substance, but it is thought that by surrounding the calcium carbonate with an amorphous body, it contributes to strength improvement by actions such as inhibiting the progress of cracks. The content of calcium carbonate is desirably 48% by weight or less based on the total weight of the amorphous body. The reason for this is that if it exceeds 48% by weight, the bending strength is reduced. 0.1% by weight
The above is desirable. If the content is less than 0.1% by weight, it does not contribute to the improvement in strength.

Here, when the specific gravity of the amorphous powder is less than 2.2, the hardness and strength become low, while when it exceeds 3.0, it becomes brittle, which also leads to a decrease in strength.
It is preferably in the range of 3.0 to 3.0.

The above amorphous powders are used in various industries, for example, fillers for decorative boards, raw materials for inorganic boards, filter materials, column packing materials for chromatography, catalyst carriers, artificial bone raw materials, artificial limb materials It can be applied to a resin filler for sealing electronic parts, a filler for a resist composition, and the like.

As the amorphous powder, a powder obtained by firing industrial waste is recommended, and a powder obtained by firing paper sludge (scum) is most preferable. That is,
Papermaking sludge is a pulp residue containing an inorganic substance, which is low in cost because industrial waste is used as a raw material, and contributes to solving environmental problems.

This papermaking sludge has a temperature of 300.degree.
It is desirable to fire at a temperature lower than ℃. That is, 800 ° C
This is because the above tends to be crystalline, and if the temperature is lower than 300 ° C., the pulp is only carbonized and powder cannot be obtained. Also,
An amorphous structure can also be obtained by firing papermaking sludge at 300 to 1500 ° C and then quenching.

Further, in order to make the amorphous powder porous and have a specific surface area of 1.6 to 200 m ² / g, it is desirable to treat the surface with an alkaline aqueous solution or the like.

In the papermaking sludge, in addition to pulp, Al, Si, Ca, Na, Mg, P, S, K, T
An oxide, a hydroxide or a precursor thereof, such as i, Mn, Fe and Zn, or a sol thereof, or a composite thereof, at least one selected from halogen and calcium carbonate, and water. , In general. In particular, waste paper of high quality paper contains a large amount of calcium-based crystals such as kaolin and calcium carbonate. Therefore, paper sludge containing a large amount of waste paper is suitable.

The water content in the papermaking sludge is from 20 to
Desirably, it is 80% by weight. This is because if the water content is less than 20% by weight, it becomes too hard and molding becomes difficult, while if it exceeds 80% by weight, it becomes a slurry and molding becomes difficult.

By the way, various techniques using papermaking sludge can be found, but all of them have different technical contents from the present invention. That is, JP-A-49-86438 discloses that
A hot-pressed mixture of pulp scum (cellulose component) and lime scum is disclosed, but pulp scum means cellulose and uses the inorganic component in papermaking sludge as in the present invention. However, it is not a dispersion of fibers in inorganic amorphous. For this reason, fracture at the grain boundaries of limescale or crack propagation cannot be prevented, and problems remain in bending strength and compressive strength. Moreover, the limescale is
Crystalline substance (calcium oxide) burned from paper pulp
Which is clearly distinguished from the amorphous body of the present invention.

Further, JP-A-7-47537 and JP-A-7-6
9701, 6-293546 and 5-270
No. 872 discloses a technique of combining cement and inorganic reinforcing fibers, and JP-A-10-15923 discloses a technique of mixing pulp sludge with crystalline gypsum.
Japanese Patent Application Laid-Open No. 9-2880 discloses a technique which focuses only on fibers in pulp waste, and Japanese Patent Application Laid-Open No. 53-81388 discloses a fiber in pulp waste (20% fiber, 0.01% earth and sand).
Each of the techniques described above is different from a technique in which a fibrous substance is dispersed in an inorganic amorphous material as in the present invention.

Furthermore, Japanese Patent Application Laid-Open No. 51-30088 describes a technique for forming baked ash of pulp waste and a lightweight inorganic material, but does not describe calcination conditions and the like. Cannot be obtained. JP-A-8-2
No. 46400 discloses a technique in which waste paper pulp itself is used instead of papermaking sludge. JP-A-48-443
No. 49 discloses a technique in which a pulp waste containing an organic substance and an inorganic substance is mixed with a polymer emulsion or the like. The term "inorganic" refers to silicon oxide, aluminum oxide and iron oxide. And two or more metal oxides as in the present invention are different from those constituting a complex amorphous system. And, JP
JP-A-99524 discloses a ceramic (polycrystalline) base material, which is different from an amorphous base material as in the present invention.

Next, a composite cured product prepared from the amorphous powder of the present invention will be described. As described above, the composite cured product using the amorphous powder of the present invention is preferably prepared by adding the amorphous powder, a binder, and if necessary, a fibrous material. The binder used here is desirably composed of one or both of a thermosetting resin and an inorganic binder. As the thermosetting resin, one or more resins selected from phenol resins, melamine resins, epoxy resins and urea resins are desirable. As the inorganic binder, at least one selected from the group consisting of sodium silicate, silica gel and alumina sol is desirable. Furthermore, unfired papermaking sludge can be used as a binder.

The fibrous material mixed in the composite cured product may be either organic or inorganic. As the organic fibrous material, at least one selected from synthetic fibers such as vinylon, polypropylene, and polyethylene, and organic fibrous materials composed of polysaccharides can be used, and organic fibrous materials composed of polysaccharides are preferable. . This is because OH groups exist in polysaccharides, and Al ₂
This is because it is easy to bond with various compounds of O ₃ , SiO ₂ or CaO.

The polysaccharide is desirably at least one compound selected from amino sugars, uronic acids, starch, glycogen, inulin, lichenin, cellulose, chitin, chitosan, hemicellulose and pectin.
As the organic fibrous material composed of these polysaccharides, pulp, pulp grounds, and crushed waste paper such as newspapers and magazines are advantageously suited.

On the other hand, as the inorganic fibrous material, one or more selected from alumina whiskers, SiC whiskers, silica-alumina-based ceramic fibers, glass fibers, carbon fibers, and metal fibers can be used.

The content of the fibrous material is desirably 2 to 75% by weight based on the total weight of the composite cured product. The reason for this is that if the amount is less than 2% by weight, the strength of the composite cured body is reduced, and if it exceeds 75% by weight, the fire protection performance, water resistance, dimensional stability and the like may be reduced. Further, the average length of the fibrous material is desirably 10 to 3000 μm. If the average length is too short, no entanglement occurs, and if the average length is too long, voids are formed, and the strength of the inorganic cured product tends to decrease.

On the other hand, the content of the amorphous powder in the composite cured product is preferably 10 to 90% by weight based on the total weight of the composite cured product. This is because if the content of the amorphous powder is out of the above range, the desired strength cannot be obtained.

Further, in addition to the amorphous powder, an inorganic powder may be added to the composite cured product. Specifically, at least one selected from calcium carbonate, calcium hydroxide, shirasu, shirasu balloon, perlite, aluminum hydroxide, silica, alumina, talc, calcium carbonate, kaolinite and industrial waste powder can be used. In particular, as the industrial waste powder, it is desirable to use at least one type of industrial waste powder selected from calcined powder of papermaking sludge, grinding dust of glass, and crushed silica sand. This is because by using these industrial waste powders, cost reduction can be realized and furthermore, it can contribute to solving environmental problems.

The above-mentioned composite hardened materials are used in various industries and include medical materials for artificial limbs, artificial bones and artificial roots, including new building materials replacing calcium silicate plates, perlite boards, plywood, gypsum boards and the like. It can be used for electronic materials such as a core substrate of a printed wiring board and an interlayer resin insulating layer.

Next, as one application example of this composite cured product,
The composite building material will be described below. That is, FIG.
In a composite building material in which a reinforcing layer 5 is formed on at least one surface of the core material 4 and on both surfaces in the illustrated example, as shown in FIG. Features. That is, by using the core 4 as the composite cured body 2 of the present invention, even when a tensile force is applied to the core, the core itself has excellent bending strength.
In addition, the reinforcing layer is provided on the surface of the core material, so that the structure is not easily broken. Also,
Even if pressure is locally applied to the surface, no dent or depression occurs.

Further, the composite building material of the present invention is provided with a decorative layer such as a coating, a decorative panel and a decorative veneer on the reinforcing layer 5 upon its use. Scratches such as dents are less likely to occur, and the decorative surface is not distorted by the scratches and the design is not degraded.

The reinforcing layer 5 has a structure in which the fiber base material 5b is embedded in the resin 5a. It is particularly desirable to use a thermosetting resin for the resin 5a. That is, unlike a thermoplastic resin, a thermosetting resin has excellent fire resistance and does not soften even at a high temperature, so that the function as a reinforcing layer is not lost. As the thermosetting resin, a phenol resin, a melamine resin, an epoxy resin, a polyimide resin, a urea resin and the like are suitable. In order to impart sufficient rigidity, impact resistance, and even higher fire resistance to the reinforcing layer, the content of the thermosetting resin in the reinforcing layer is desirably in the range of 10% by weight to 65% by weight.

On the other hand, it is desirable to use inorganic fibers for the fiber base material 5b. This is because the strength of the reinforcing layer 5 can be improved and the coefficient of thermal expansion can be reduced. It is preferable to use glass fiber, rock wool, and ceramic fiber as the inorganic fiber because they are low in cost and have excellent heat resistance and strength. This fiber base material is a material obtained by molding a discontinuous fiber into a mat shape, or a material obtained by cutting continuous long fibers into a mat shape by cutting into 3 to 7 cm (a so-called chopped strand mat), and dispersing in water to form a sheet. A material obtained by piling up, a continuous long fiber spirally laminated to form a mat, or a continuous long fiber woven is applicable.

Further, the thickness of the reinforcing layer is from 0.2 mm to
It is desirable to be 3.5 mm. This is because, if it is set in this range, sufficient rigidity and impact resistance can be obtained, and high workability can be maintained. The reinforcing layer may contain a flame retardant such as aluminum hydroxide and magnesium hydroxide, and a commonly used inorganic binder such as silica sol, alumina sol, and water glass.

The method for producing the amorphous powder of the present invention, and the method for producing the composite cured product and the composite building material will be described below. First, a method for producing an amorphous powder is as follows. First, paper sludge is prepared as a raw material. This papermaking sludge includes printing and information paper,
Kraft paper, titanium paper, tissue paper, dust paper,
It is desirable to use papermaking sludge discharged from a pulp manufacturing process, a raw material processing process, a papermaking process, and the like when manufacturing toilet paper, sanitary products, towel paper, industrial hybrid paper, and household hybrid paper. As commercially available papermaking sludge, “raw sludge” handled by Maruto Kiln Co., Ltd. can be used.

After the papermaking sludge is dewatered, it is calcined at 300 ° C. or more and less than 800 ° C. for 30 minutes to 10 hours, and the calcined sludge is pulverized with a ball mill or a mixer. Can be obtained.

Next, a method for producing a composite cured product will be described.
That is, the amorphous powder is mixed with a binder and, if necessary, a fibrous material to prepare a raw material mixture. Here, when unfired papermaking sludge is used, since the sludge contains an inorganic substance and pulp, the binder and the fibrous material can be mixed at the same time, which is advantageous. The raw material mixture is poured into a desired mold, or into a mold provided with a filter, and then pressed to remove moisture, or formed into a slurry by mixing the raw material mixture. After this molding, drying and curing are performed at a heating temperature of 20 to 160 ° C. to obtain a composite cured product. In addition, if the heating temperature is too high, deformation or cracks are generated, and if it is too low, it takes a long time for drying, and productivity is lowered, which is not preferable.

In particular, to mold the composite cured product into a plate shape,
The papermaking sludge is formed into a sheet by a known method such as circular net forming, fourdrinier forming, dewatering press forming, extrusion forming, etc. And dried, and the sheet-shaped molded body is pressed while being heated at a heating temperature of 80 to 160 ° C.,
It is formed into a plate-shaped core material. The pressure at that time is 1 to 120 kg
f / cm ² is appropriate.

Here, the term "pressing" refers to maintaining the pressure applied. Then, the fibrous material is oriented in a direction crossing the pressing direction by the pressure applied at the time of pressing, so that the bending strength of the core material can be improved. In addition, the pressurization removes moisture and suppresses the progress of crystallization, which is advantageous for forming an amorphous body.

Further, the inorganic powder can be dispersed in the composite cured product by adding and mixing the inorganic powder to the papermaking sludge and then heating and curing the mixture.

In addition to the papermaking sludge, metal alkoxides and metal hydroxides can be used as raw materials. For example, a mixture of alkoxides and hydroxides of Al, Si and Ca and a crushed material obtained by crushing waste paper are mixed, and the mixture is hydrolyzed and polymerized in the presence of an acid or alkali to form a sol. May be gelled. Such gels result in Al ₂ O ₃ , SiO ₂ , Ca
O, Na ₂ O, MgO, P ₂ O ₅ , SO ₃ , K ₂ O, T
It is presumed to be the same as a compound obtained by solid solution or hydration reaction of an oxide such as iO ₂ , MnO, Fe ₂ O ₃ and ZnO.

The composite building material is manufactured as follows. First, the papermaking sludge is formed into a sheet by a known method such as circular net forming, fourdrinier forming, dewatering press forming, and extrusion forming, and dried, or while the sludge is conveyed by a conveyor, the sheet is pressed by a roll. It is a shaped body. On the other hand, the fiber base material is impregnated with a resin, heated at 25 to 70 ° C., and dried to obtain a reinforcing sheet. Next, the sheet-shaped molded body and the reinforcing sheet are laminated, and pressed while heating,
It is molded into a composite building material consisting of a core material (composite cured body) and a reinforcing layer. It is appropriate that the heating temperature here is 80 to 200 ° C. and the pressure is about 1 to ²⁰ kgf / cm ² .

Instead of the above method, a mat of inorganic fibers is impregnated with a resin composition, dried, heated and pressed, and the thermosetting resin is cured to form a reinforcing layer.
A method of attaching this reinforcing layer to a core material which has been cured in advance with an adhesive may be used. Further, a thermosetting resin, for example, at least one thermosetting resin selected from phenol resin, melamine resin, epoxy resin, urea resin and urethane resin may be applied to the surface of the core material 4.

Further, the surface of glass fiber, rock wool or ceramic fiber is coated with a thermosetting resin such as a phenol resin in another configuration, and a fiber base made of these fibers is laminated on a sheet-like molded body. And hot pressing. This method of coating the fiber surface with a thermosetting resin in a separate step is advantageous because the adhesion to the impregnated resin is improved, the fibers are easily bonded to each other, and the resin impregnation rate can be further improved. . As a method of such coating, a method of impregnating the fiber base material with an uncured thermosetting resin and drying,
Alternatively, there is a method in which a raw material melt of glass fiber, rock wool or ceramic fiber is discharged from a nozzle, fiberized by a blowing method or a centrifugal method, and a solution of a thermosetting resin such as a phenol resin is sprayed simultaneously with the fiberization. .

When a glass fiber, rock wool, or ceramic fiber is used as a constituent material of the fiber base material, it is preferable to coat a silane coupling agent. The surface of the composite building material obtained in this way,
The back surface can be painted, or a decorative plate or a decorative veneer can be attached with an adhesive or the like. The coating is performed by printing and spraying various pigments, inks, and the like. The decorative board is a three-layer decorative board including a phenol resin-impregnated core layer, a melamine resin-impregnated pattern layer, and a melamine resin-impregnated overlay layer, a melamine resin-impregnated backer layer, a phenol resin-impregnated core layer, and a melamine resin-impregnated pattern layer. And a decorative plate having a four-layer structure composed of an overlay layer impregnated with a melamine resin. In particular, in the case of a decorative board having a phenolic resin-impregnated core layer as the core layer, the surface strength is significantly increased, so that it can be applied to flooring materials and the like. In addition, high quality wood such as cedar and cypress can be used as the decorative veneer.

[0065]

EXAMPLES (Example 1) Unfired papermaking sludge ("raw sludge" handled by Maruto Kiln Co., Ltd .: solid content 34% by weight, moisture 66)
% By weight) is dried at 80 ° C. while stirring,
After the obtained dried body was calcined at 780 ° C. for 5 hours, it was immediately exposed to room temperature and rapidly cooled. Further, the fired product was ball-milled for 5 hours to obtain 248 g of amorphous powder.

This amorphous powder was converted into a fluorescent X-ray analyzer (Ri
Analysis using GIX RIX2100) revealed that the composition was as follows in terms of oxide. The specific surface area was measured according to JIS R-1626 (BET method: one-point method of flow method). SiO ₂ : 34.1% by weight, Fe ₂ O ₃ : 1.6% by weight CaO: 32.1% by weight, TiO ₂ : 1.0% by weight Al ₂ O ₃ : 20.7% by weight, SO ₃ : 0.5 wt% MgO: 5.9 wt%, Cl: 0.2% by weight P ₂ O _5: 2.8 wt%, ZnO: 0.1 wt% Others: trace average particle size: 11.0 .mu.m true specific gravity : 2.756 Specific surface area: 19.0 m ² / g

Further, the crystal structure was confirmed by X-ray diffraction. FIG. 4 shows a chart of the X-ray diffraction. Note that X
The line diffraction used Rigaku MiniFlex and targeted Cu. A gentle undulation (halo) is observed around 2θ: 22 °, and a peak indicating a crystal structure is also observed, indicating that the crystal structure is mixed in the amorphous structure. From the peak, Gehlenite, syn, Melitite
-synthetic, Gehlenite-synthetic, Anorthite, orde
red has been identified. The amount of crystals present is about 2
It was 0% by weight.

Next, the thus obtained amorphous powder 24
8 parts by weight and 1512 parts by weight of unfired papermaking sludge are kneaded, and while the kneaded material is conveyed on a conveyor, 35 kg
While applying a pressure of f / cm ² , a sheet-shaped molded body having a thickness of 10 mm was obtained. This sheet-like molded body was heated at 100 ° C. to obtain a plate-shaped composite cured body.

Incidentally, the side surface of the composite cured product was examined with an optical microscope (5
(0x), the fibers were oriented in a direction perpendicular to the pressing direction.

(Example 2) The fired product obtained in Example 1 was ball-milled for 10 hours to obtain 248 g of an amorphous powder. This amorphous powder is converted into a fluorescent X-ray analyzer (Rigaku
RIX2100), the composition was as follows. SiO ₂ : 34.1% by weight, Fe ₂ O ₃ : 1.6% by weight CaO: 32.1% by weight, TiO ₂ : 1.0% by weight Al ₂ O ₃ : 20.7% by weight, SO ₃ : 0.5 wt% MgO: 5.9 wt%, Cl: 0.2% by weight P ₂ O _5: 2.8 wt%, ZnO: 0.1 wt% Others: trace average particle size: 6.6 [mu] m true specific gravity : 2.756 Specific surface area: 31.7 m ² / g

Next, the thus obtained amorphous powder 24
8 parts by weight and 1512 parts by weight of unfired papermaking sludge are kneaded, and while the kneaded material is conveyed on a conveyor, 35 kg
While applying a pressure of f / cm ² , a sheet-shaped molded body having a thickness of 10 mm was obtained. This sheet-like molded body was heated at 100 ° C. to obtain a plate-shaped composite cured body.

Example 3 The calcined product obtained in Example 1 was ball-milled for 3 hours to obtain 248 g of an amorphous powder. This amorphous powder is converted into a fluorescent X-ray analyzer (Rigaku
RIX2100), the composition was as follows. SiO ₂ : 34.0 wt%, Fe ₂ O ₃ : 12.6 wt% CaO: 32.1 wt%, TiO ₂ : 1.0 wt% Al ₂ O ₃ : 20.7 wt%, SO ₃ : 0.5 wt% MgO: 6.0 wt%, Cl: 0.2% by weight P ₂ O _5: 2.7 wt%, ZnO: 0.1 wt% Others: trace average particle size: 17.6Myuemu true specific gravity : 2.756 Specific surface area: 4.8 m ² / g

Next, the thus obtained amorphous powder 24
8 parts by weight and 1512 parts by weight of unsintered papermaking sludge are kneaded, and while the kneaded material is conveyed on a conveyor, 50 kg
While applying a pressure of f / cm ² , a sheet-shaped molded body having a thickness of 10 mm was obtained. This sheet-like molded body was heated at 100 ° C. to obtain a plate-shaped composite cured body.

Example 4 The amorphous powder obtained by ball milling in Example 1 was further ball milled for 30 hours to obtain 248 g of amorphous powder. When this amorphous powder was analyzed using an X-ray fluorescence analyzer (Rigaku RIX2100), it was converted to oxide and had the following composition. SiO ₂ : 34.0 wt%, Fe ₂ O ₃ : 12.6 wt% CaO: 32.1 wt%, TiO ₂ : 1.0 wt% Al ₂ O ₃ : 20.7 wt%, SO ₃ : 0.5 wt% MgO: 6.0 wt%, Cl: 0.2% by weight P ₂ O _5: 2.7 wt%, ZnO: 0.1 wt% Others: trace average particle size: 1.5 [mu] m true specific gravity : 2.756 Specific surface area: 139 m ² / g

Next, the thus obtained amorphous powder 24
8 parts by weight and 1512 parts by weight of unfired papermaking sludge are kneaded, and while the kneaded material is conveyed on a conveyor, 3 kgf
/ Cm ² while applying a pressure of 10 mm / cm ² to obtain a sheet-shaped molded body having a thickness of 10 mm. This sheet-like molded body was heated at 100 ° C. to obtain a plate-shaped composite cured body.

Comparative Example 1 The amorphous powder obtained by ball milling in Example 1 was further ball milled for 48 hours to obtain 248 g of amorphous powder. When this amorphous powder was analyzed using an X-ray fluorescence analyzer (Rigaku RIX2100), it was converted to oxide and had the following composition. SiO ₂ : 34.0 wt%, Fe ₂ O ₃ : 12.6 wt% CaO: 32.1 wt%, TiO ₂ : 1.0 wt% Al ₂ O ₃ : 20.7 wt%, SO ₃ : 0.5 wt% MgO: 6.0 wt%, Cl: 0.2% by weight P ₂ O _5: 2.7 wt%, ZnO: 0.1 wt% Others: trace average particle diameter: 0.98 .mu.m true specific gravity : 2.756 Specific surface area: 213 m ² / g

Next, the thus obtained amorphous powder 24
8 parts by weight and 1512 parts by weight of unfired papermaking sludge are kneaded, and while the kneaded material is conveyed on a conveyor, 3 kgf
/ Cm ² while applying a pressure of 10 mm / cm ² to obtain a sheet-shaped molded body having a thickness of 10 mm. This sheet-like molded body was heated at 100 ° C. to obtain a plate-shaped composite cured body.

Comparative Example 2 The fired product obtained in Example 1 was ball-milled for 10 minutes to obtain 248 g of an amorphous powder. This amorphous powder is converted into a fluorescent X-ray analyzer (Rigaku
RIX2100), the composition was as follows. SiO ₂ : 34.0 wt%, Fe ₂ O ₃ : 12.6 wt% CaO: 32.1 wt%, TiO ₂ : 1.0 wt% Al ₂ O ₃ : 20.7 wt%, SO ₃ : 0.5 wt% MgO: 6.0 wt%, Cl: 0.2% by weight P ₂ O _5: 2.7 wt%, ZnO: 0.1 wt% Others: trace average particle size: 232Myuemu true specific gravity: 2 .756 Specific surface area: 0.9 m ² / g

Next, the thus obtained amorphous powder 24
8 parts by weight and 1512 parts by weight of unfired papermaking sludge are kneaded, and while the kneaded material is conveyed on a conveyor, 3 kgf
/ Cm ² while applying a pressure of 10 mm / cm ² to obtain a sheet-shaped molded body having a thickness of 10 mm. This sheet-like molded body was heated at 100 ° C. to obtain a plate-shaped composite cured body.

(Example 5) 248 parts by weight of the amorphous powder obtained in Example 1 and 62 parts by weight of a phenol resin were kneaded, and while this kneaded product was conveyed on a conveyor, 3 kgf /
While applying a pressure of ² cm ² , a sheet-shaped molded product having a thickness of 10 mm was obtained. The sheet-shaped molded body was pressed at a temperature of 180 ° C. and a pressure of 28 kgf / cm ^{2 for} 20 minutes to obtain a composite cured body.

Example 6 After a sheet-like glass fiber was impregnated with a phenol resin solution obtained by adding a curing agent (impregnation amount: 45% in terms of solid content), it was dried at a temperature of 80 ° C. for 20 minutes to obtain a reinforcing sheet. Obtained. Next, a sheet-like molded body was produced in the same manner as in Example 1. Then, the reinforcing sheet is placed on the front and back surfaces of the sheet-shaped molded body, and pressed at a temperature of 110 ° C. for 20 minutes at a pressure of 7 kgf / cm ² , and a reinforcing layer having a thickness of 1 mm and a reinforcing layer having a thickness of 10 mm are formed on both sides. A composite building material consisting of a core material was manufactured. Further, a decorative veneer of cedar board having a thickness of 0.2 mm was attached to the surface of the composite building material via a vinyl acetate adhesive.

(Comparative Example 3) A slurry was prepared by mixing 60 parts by weight of fired scum fired at 1000 ° C, 36 parts by weight of water, 100 parts by weight of cement, and 0.3 parts by weight of vinylon fiber for 3 minutes with a forced stirring mixer. The slurry was poured into a mold, pressurized at 150 to 180 kgf / cm ² , and then demolded. When X-ray diffraction measurement was performed on the powder collected from the plate-like body, Gehlenite, syn, Melitite-synth
Only etic, Gehlenite-synthetic, Anorthite, and ordered peaks were observed.

(Comparative Example 4) A lime-based sewage sludge molten slag (manufactured by Osaka City Sewerage Corporation, whose main chemical component is as follows) was fired at 1500 ° C, and the fineness was 3500 cm ² / blaine in a ball mill. g, 5 parts by weight, and 95 parts by weight of ordinary Portland cement (made by Chichibu Onoda) are mixed.
_The mixed cement composition was manufactured by adjusting with natural gypsum so that the amount of ₃ became 2% by weight. This cement and sand:
The mixture was mixed at a ratio of 3 and left for 3 days. Serial SiO _2: 33.4 wt%, MgO: 2.4 wt% Al ₂ O _3: 14.2 wt%, P ₂ O _5: 7.0 wt% Fe ₂ O _3: 5.0 wt%, NaO : 0.7% by weight CaO: 33.9% by weight, K ₂ O: 0.7% by weight

The cured composites or composite building materials obtained in the above Examples and Comparative Examples were tested for flexural strength, compressive strength, workability and nailability. Table 1 shows the results.
Shown in The test method was such that the bending strength was JIS A69.
01, and the compressive strength was measured according to the method specified in JISA 5416, respectively. The workability is
Cutting was performed with a circular saw for woodworking, and workability was determined. Further, regarding the nailing property, a diameter of 4 mm and a length of 50 mm
The nail was hit and the depth of nail penetration and the presence or absence of cracks were examined.

[0085]

[Table 1]

[0086]

As described above, the composite cured product produced using the amorphous powder of the present invention is an inexpensive material having excellent workability and productivity, particularly having high bending strength. It can be applied advantageously in various fields, and in particular, can be driven into nails, so that it is possible to provide low-cost raw materials optimal for building materials.

[Brief description of the drawings]

FIG. 1 is a schematic cross-sectional view of a composite cured product manufactured using the amorphous powder of the present invention.

FIG. 2 is a schematic cross-sectional view of a composite cured product manufactured using the amorphous powder of the present invention.

FIG. 3 is a schematic sectional view of a composite building material manufactured using the amorphous powder of the present invention.

FIG. 4 is a chart of X-ray diffraction of the amorphous powder of Example 1.

[Description of Signs] 1 Amorphous body 2 Composite cured body 3 Fibrous material 4 Core material 5 Reinforcement layer

 ──────────────────────────────────────────────────続 き Continuing from the front page (72) Inventor Kenji Sato 1- 1 north of Ibigawa-cho, Ibi-gun, Gifu Prefecture Inside the Ogaki-kita Plant (72) Inventor Toshihiro Nomura 1- 1 north of Ibigawa-cho, Ibi-gun, Gifu F Term in Ogaki Kita Factory (reference) AG44 AG95 AG99 AH37 BF02 BG04 EA17 FA13 FA20 GA21 GA38

Claims (6)

[Claims] 1. A porous powder containing an inorganic amorphous material, having a specific surface area of 1.6 to 200 m ² / g. 2. A porous powder containing an amorphous body composed of two or more oxides, having a specific surface area of 1.6 to 2.
An amorphous powder characterized by being 200 m ² / g. 3. A composite cured product comprising the amorphous powder according to claim 1 and a binder. 4. A composite cured product comprising the amorphous powder according to claim 1 and a binder and a fibrous material. 5. The composite cured product according to claim 4, wherein the fibrous material is oriented. 6. A composite building material in which a reinforcing layer is formed on at least one surface of a core material, wherein the core material is provided with a reinforcing layer.
A composite building material characterized by applying the composite cured product according to any one of the above.