JP2016107275A - Mold wash composition for lost foam pattern - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a mold wash composition for a lost foam pattern having high safely, and capable of suppressing furthermore residual defects; and to provide a manufacturing method of a cast.SOLUTION: There are provided a mold wash composition for a lost foam pattern including a refractory aggregate and amorphous cellulose, and a manufacturing method of a lost foam pattern for a cast having a coating film around the lost foam pattern. The manufacturing method of a lost foam pattern for a cast has a step for forming a coating film by attaching a mold wash composition for a lost foam pattern to the periphery of the lost foam pattern.SELECTED DRAWING: Figure 1

Description

  The present invention relates to a coating agent composition for disappearance model to be attached around the disappearance model.

  The vanishing model casting method is a casting method in which a synthetic resin foam model of the same shape as the product is replaced with molten metal (hereinafter also referred to as “molten metal”). No core or complicated work such as mold matching is required. This casting method has been attracting attention in recent years because it has many advantages such as easy delivery and quick delivery. In this casting method, the synthetic resin foam is thermally decomposed by the cast molten metal, so that there is a defect that a residue defect occurs in the casting due to a large amount of generated pyrolysis gas and residue. In particular, when polystyrene is used as the synthetic resin foam, the casting surface is deteriorated by the carbonized component.

  In the disappearance model casting method, the disappearance model coating agent has “residue defects” caused by thermal decomposition of the synthetic resin foam model, and “baking defects” in which the molten metal breaks the coating film and leaks into the sand mold. Used to prevent.

  Residual defects are a phenomenon in which, when the synthetic resin foam model is replaced with molten metal, when the pyrolysis gas is insufficiently discharged, it becomes a pyrolysis residue and is caught in the upper part of the product. In order to prevent the “residue defect”, it is required to efficiently discharge the pyrolysis gas of the synthetic resin foam model to the mold side. About "baking defects", it is required to keep the film as a strong film until the solidification of the molten metal is completed.

  As a conventional disappearance model coating composition, for example, Patent Document 1 discloses a nitrocellulose that is insoluble in water and soluble in a hydrophilic organic solvent. The disappearance model coating composition is a water-hydrophilic organic solvent system that selects a substance that is finely dispersed in white turbidity, and finely disperses nitrocellulose in the coating liquid to reduce residual defects. is there. Patent Document 2 describes a coating agent composition that contains organic particles to reduce residual defects.

Japanese Patent Laid-Open No. 3-180244 Japanese Patent Laid-Open No. 2001-1104

  However, the conventional disappearance model coating composition has not been sufficiently prevented from residual defects, and further improvement has been demanded. Moreover, since the coating agent composition for disappearance models according to Patent Document 1 uses nitrocellulose, there is a problem in safety.

  This invention provides the coating agent composition for disappearance models which is high in safety and can further suppress residue defects.

  The disappearance model coating composition of the present invention contains a fireproof aggregate and amorphous cellulose.

  ADVANTAGE OF THE INVENTION According to this invention, the coating agent composition for disappearance models which can be highly safe and can suppress a residue defect more can be provided.

It is the schematic of the vanishing model used for evaluation of an Example.

<Coating agent composition for disappearance model>
The vanishing model coating composition of the present embodiment (hereinafter also simply referred to as “coating composition”) contains a refractory aggregate and amorphous cellulose. According to the vanishing model coating agent composition of the present embodiment, there is an effect that safety is high and residue defects can be further suppressed. The reason for such an effect is not clear, but is considered as follows.

  In order to prevent residue defects, it is important to efficiently discharge the pyrolysis gas of the synthetic resin foam model from the coating film until the casting is completed. In the coating composition according to the present embodiment, since the non-crystalline cellulose is contained in the refractory aggregate of the coating composition, the non-crystalline cellulose is dispersed in the coating film. Since the amorphous cellulose burns and disappears due to heat at the time of casting, the portion where the amorphous cellulose is present becomes a void. This void becomes a gas hole, and the pyrolysis gas of the synthetic resin foam can be efficiently discharged, so that it is considered that residual defects can be reduced.

  Hereinafter, the components contained in the disappearance model coating agent composition of the present embodiment will be described.

(Fireproof aggregate)
The mold agent composition according to the present embodiment contains a refractory aggregate. As the refractory aggregate, a refractory aggregate that has been conventionally used according to the purpose of casting can be used. Examples of refractory aggregates include mica, obsidian, pearlite, pinestone, orthofeldspar, feldspar, leucite, aragonite, silica, alumina, mullite, shaft banquet, diaspore, spinel, magnesia, olivine, talc , Calcined zircon, kaolin, silimanite, andalusite, kyanite, gibbsite, black sandstone, decaitite, anorthite, graphite bauxite, and the like. The said fireproof aggregate can be used by said 1 type, or 2 or more types.

  The average particle diameter of the refractory aggregate is preferably 20 μm or more, more preferably 40 μm or more, and still more preferably 50 μm or more from the viewpoint of preventing residual defects. The average particle size of the refractory aggregate is preferably 400 μm or less, more preferably 200 μm or less, and even more preferably 150 μm or less from the viewpoint of preventing seizure defects. Moreover, 20-400 micrometers is preferable, as for the average particle diameter of a refractory aggregate, 40-200 micrometers is more preferable, and 50-150 micrometers is still more preferable. In addition, the average particle diameter of the said refractory aggregate is measured by the method as described in an Example.

  The content of the fireproof aggregate in the coating composition of the present embodiment is preferably 30% by mass or more, and more preferably 40% by mass or more, from the viewpoint of preventing coating film defects such as drying property and cracks. The content of the refractory aggregate in the coating composition of the present embodiment is preferably 80% by mass or less, and more preferably 70% by mass or less, from the viewpoint of application workability. Moreover, 30-80 mass% is preferable and, as for content of the refractory aggregate of the coating agent composition of this embodiment, 40-70 mass% is more preferable.

[Amorphized cellulose]
The non-crystallized cellulose is cellulose in which the crystal structure of cellulose, which is a carbohydrate (polysaccharide) represented by the molecular formula (C ₆ H ₁₀ O ₅ ) n, is amorphized.

  In the present specification, non-crystalline cellulose means cellulose having a crystallinity of 33% or less.

In this specification, the crystallinity of cellulose is cellulose I-type crystallinity calculated by the Segal method from the diffraction intensity value by the X-ray diffraction method, and is defined by the following calculation formula (A).
Cellulose type I crystallinity (%) = [(I _22.6 -I _18.5 ) / I _22.6 ] × 100 (A)
_{Wherein, I 22.6} is a diffraction intensity of the lattice plane in X-ray diffraction (002 plane) (diffraction angle 2θ = 22.6 _{°), I 18.5} is amorphous portion (angle of diffraction 2 [Theta] = 18.5 (Shows the diffraction intensity of °)

  Here, the cellulose I type crystallinity is determined by the diffraction angle 22.6 ° (peak corresponding to the 002 plane representing crystallinity) and 18.5 ° (12.5 °) of the X-ray diffraction pattern as shown in the above calculation formula (A). The peak intensity I of the peak corresponding to the amorphous part is used. As amorphization progresses, I22.6 <I18.5 may eventually be obtained (that is, a negative value is calculated according to this definition), while the upper limit of cellulose I-type crystallinity is 100%. The cellulose type I is a natural cellulose crystal form.

  From the viewpoint of suppressing residual defects, the crystallinity is preferably 30% or less, more preferably 25% or less, and still more preferably 20% or less. The crystallinity is preferably −30% or more, more preferably −20% or more, and still more preferably −10% or more from the viewpoint of the cost of the amorphous treatment. The crystallinity is preferably −30% to 30%, more preferably −20% to 25%, and still more preferably −10% to 20%.

  Two or more kinds of celluloses having different crystallinity levels may be used in combination. In this case, the crystallinity degree of cellulose means a crystallinity degree determined by a weighted average of the cellulose used, and the value is It is preferable to be within the range.

  In order to form gas holes after the cellulose dispersed in the coating film is burnt out, the gas holes are burned out at 250 to 400 ° C., which is the temperature of the gas layer at the time of casting, and exist until the casting is finished. It is necessary. For this reason, amorphous cellulose that decomposes at 250 to 400 ° C. and has a low residual carbon ratio and low ash content after decomposition is preferable.

  The shape of the non-crystallized cellulose is not particularly limited, and a fibrous or particulate shape can be used. From the viewpoint of coating workability, a particulate shape is preferable.

  When the amorphous cellulose has a particulate shape, the average particle size of the amorphous cellulose is preferably 50 μm or more, more preferably 80 μm or more, from the viewpoint of reducing residual defects. In addition, the average particle size of the amorphous cellulose is preferably 500 μm or less, and more preferably 200 μm or less, from the viewpoint of reducing the deposition defects. Moreover, 50-500 micrometers is preferable and, as for the average particle diameter of the said amorphous cellulose, 80-200 micrometers is more preferable. In addition, in this specification, an average particle diameter is measured by the method as described in an Example.

  When the amorphous cellulose has a fibrous shape, the fiber length of the amorphous cellulose is preferably 50 μm or more, more preferably 80 μm or more, and still more preferably 120 μm or more from the viewpoint of reducing residual defects. In addition, the fiber length of the amorphous cellulose is preferably 600 μm or less, and more preferably 300 μm or less, from the viewpoint of reducing seizure defects. The fiber length of the amorphous cellulose is preferably 50 to 600 μm, more preferably 80 to 300 μm, and still more preferably 120 to 300 μm.

  When the amorphous cellulose has a fibrous shape, the fiber diameter of the amorphous cellulose is preferably 10 μm or more, more preferably 20 μm or more from the viewpoint of reducing residual defects. Moreover, the fiber diameter of the amorphous cellulose is preferably 80 μm or less from the viewpoint of applicability to a synthetic resin foam model. Further, the fiber diameter of the amorphous cellulose is preferably 10 to 80 μm, and more preferably 20 to 80 μm.

  The content of amorphous cellulose in the coating composition according to the present embodiment is 1 mass from the viewpoint of reducing residual defects, that is, from the viewpoint of securing voids serving as gas holes, with respect to 100 parts by mass of the refractory aggregate. Part or more, preferably 3 parts by weight or more, more preferably 4 parts by weight or more. In addition, the content of the non-crystalline cellulose in the coating composition according to the present embodiment is 12 parts by mass or less from the viewpoint of seizure defects (coating strength during heating) with respect to 100 parts by mass of the refractory aggregate. Preferably, 10 parts by mass or less is more preferable, and 7 parts by mass or less is still more preferable. Moreover, 1-12 mass parts is preferable with respect to 100 mass parts of refractory aggregates, 3-10 mass parts is more preferable, and, as for content of the non-crystalline cellulose of the coating composition which concerns on this embodiment, 4- 7 parts by mass is more preferable.

  The method for producing the non-crystalline cellulose is not particularly limited. For example, JP-A-62-2126999, JP-A-62-2127000, JP-A-62-2236801, JP-A-2003-64184. JP-A-2004-331918, JP-A-4160108, JP-A-4160109, JP-A-2011-1547, and the like.

[Dispersion medium]
In the disappearance model casting method of the present embodiment, since the voids after the non-crystalline cellulose is burnt and disappeared by heat at the time of casting are gas holes, when a dispersion medium that dissolves the non-crystalline cellulose is used, the gas It is difficult to form voids that become holes. Therefore, the dispersion medium preferably does not dissolve the amorphous cellulose.

  As the dispersion medium, for example, alcohols or water can be used.

  In the case of an alcoholic coating composition, lower alcohols such as methanol, ethanol and isopropyl alcohol are preferred, and ethanol is more preferred from the viewpoint of drying properties. In the case of an alcoholic coating composition, an aromatic solvent or a hydrocarbon solvent may be used as an auxiliary dispersion medium.

  The amount of the dispersion medium in the alcoholic coating composition can be appropriately changed depending on the type of the dispersion medium used. As an example, when the said dispersion medium is a lower alcohol, 20 mass parts or more are preferable with respect to 100 mass parts of refractory aggregates, and 70 mass parts or more are more preferable from a viewpoint of application workability. In the case of a lower alcohol, the amount of the dispersion medium in the alcohol-based coating agent composition is preferably 120 parts by mass or less with respect to 100 parts by mass of the refractory aggregate, from the viewpoint of preventing coating defects such as drying properties and cracks. 110 parts by mass or less is more preferable. Moreover, if the amount of the dispersion medium in the alcoholic coating composition is a lower alcohol, it is 20 to 120 masses with respect to 100 parts by mass of the refractory aggregate from the viewpoint of forming the coating workability and a sound coating film. Part is preferable, and 70 to 110 parts by mass are more preferable.

  In the case of an aqueous coating composition, the amount of water in the aqueous coating composition is preferably 20 parts by mass or more, and 70 parts by mass or more with respect to 100 parts by mass of the refractory aggregate from the viewpoint of application workability. More preferred. In the case of an aqueous coating composition, the amount of water in the aqueous coating composition is preferably 150 parts by mass or less and more preferably 130 parts by mass or less with respect to 100 parts by mass of the refractory aggregate from the viewpoint of drying. preferable. In the case of an aqueous coating composition, the amount of water in the aqueous coating composition is preferably 20 to 150 parts by mass with respect to 100 parts by mass of the refractory aggregate from the viewpoint of application workability and drying properties. 70 to 130 parts by mass is more preferable.

[Binder]
The coating composition of the present embodiment may contain a binder as commonly used. Examples of the binder include water-soluble polymers such as sodium polyacrylate, starch, methyl cellulose, polyvinyl alcohol, sodium alginate, and gum arabic and various resin emulsions in aqueous systems. In addition, in the case of an alcohol type, it is preferable from the viewpoint of coating film strength to add various resins that are soluble or dispersed in alcohol. The content of the binder is preferably 0.5 parts by mass or more and preferably 30 parts by mass or less with respect to 100 parts by mass of the refractory aggregate from the viewpoint of coating film strength and economy. Moreover, the content of the binder is preferably 0.5 to 30 parts by mass with respect to 100 parts by mass of the refractory aggregate from the viewpoints of coating film strength and economy.

[Sintering agent]
The coating agent composition of the present embodiment may contain a sintering agent as commonly used. Examples of the sintering agent include bentonites such as sodium bentonite and calcium bentonite, clays such as kibushi clay, and ethyl silicate. Among them, bentonite is preferable because it plays a role as a sintering agent in a high temperature region in addition to a role as a binder. The addition amount of the sintering agent is preferably 0.5 parts by mass or more and more preferably 1.0 part by mass or more with respect to 100 parts by mass of the refractory aggregate from the viewpoint of coating strength at high temperatures. Moreover, the addition amount of the sintering agent is preferably 30 parts by mass or less and more preferably 15 parts by mass or less with respect to 100 parts by mass of the refractory aggregate from the viewpoint of coating strength at high temperatures. Moreover, 0.5-30 mass parts is preferable with respect to 100 mass parts of refractory aggregates, and, as for the addition amount of a sintering agent, 1.0-15 mass parts is more preferable from a viewpoint of the coating-film intensity | strength at the time of high temperature.

[Other ingredients]
Examples of other components that can be blended in the coating composition of the present embodiment include surfactants, dispersants, thixotropic agents, and the like.

  The coating composition of the present embodiment can be suitably used as a coating composition that is attached around the disappearance model.

<Manufacturing method of vanishing model for casting>
In the manufacturing method of the disappearance model for castings of this embodiment, the conventional manufacturing method of the disappearance model for castings can be applied. The method for producing a casting disappearance model of the present embodiment is a method for producing a casting disappearance model having a coating film around the disappearance model, and the disappearance model coating composition is disposed around the disappearance model. A step of forming a coating film by adhering.

  As the disappearance model to which the coating composition of the present embodiment is attached, the same model of a synthetic resin foam as usual can be used. As the synthetic resin foam, a foam such as polystyrene, polymethyl methacrylate, or a copolymer thereof is used. When the disappearance model to which the coating agent composition of this embodiment is attached is foamed polystyrene, the effect of the coating agent composition of this embodiment is further obtained. The method of forming the coating film by attaching the coating agent composition to the disappearing model is any of conventionally known methods such as flow coating (bukkake method), dipping (dipping method), brush coating, spray coating, etc. But it ’s okay.

  The disappearance model for casting obtained by the method for manufacturing the disappearance model for casting of the present embodiment can be suitably used for a method for manufacturing a mold by the disappearance model casting method.

<Manufacturing method of casting>
In the mold manufacturing method by the vanishing model casting method of the present embodiment, the mold manufacturing method by the conventional vanishing model casting method can be applied. The mold manufacturing method of the present embodiment is a casting manufacturing method using the casting disappearance model obtained by the casting disappearance model manufacturing method, wherein the casting disappearance model is embedded in foundry sand; And a step of casting molten metal into the casting disappearance model embedded in the foundry sand.

  As the foundry sand used in the step of burying the disappearance model for foundries in foundry sand, new sand or reclaimed sand such as zircon sand, chromite sand and synthetic ceramic sand is used in addition to quartz sand mainly composed of quartz. Casting sand can be used without adding a binder. In that case, the filling property is good, but when a high-strength mold is required, a conventionally known binder is added and cured with a curing agent. It is preferable to do so.

  The method for producing a mold according to the present embodiment relating to the case of adding the binder is a method for producing a casting using the disappearance model for casting obtained by the method for producing the disappearance model for casting, wherein the binder is added to the foundry sand. And a step of adding a curing agent for curing the binder and kneading to prepare a mixture, a step of embedding the casting disappearance model in the mixture, and casting a molten metal into the casting disappearance model embedded in the mixture. Including a process.

  As the binder, a binder that is usually used can be used. As the binder, for example, water-soluble polymers such as sodium polyacrylate, starch, methyl cellulose, polyvinyl alcohol, sodium alginate, gum arabic, and various resin emulsions can be used in the aqueous system. In the case of alcohols, it is preferable from the viewpoint of mold strength to add various resins that are soluble or dispersed in alcohol. The content of the binder is preferably 0.4 parts by mass or more, and more preferably 0.5 parts by mass or more with respect to 100 parts by mass of foundry sand, from the viewpoint of mold strength and economy. Moreover, 1.2 mass parts or less are preferable with respect to 100 mass parts of foundry sand, and, as for content of the said binder, from a viewpoint of casting_mold | template strength and economical efficiency, 0.8 mass parts or less are more preferable. In addition, the content of the binder is preferably 0.4 to 1.2 parts by mass, more preferably 0.5 to 0.8 parts by mass with respect to 100 parts by mass of foundry sand, from the viewpoint of mold strength and economy. .

  In the mold manufacturing method of the present embodiment, the casting temperature varies depending on the metal to be used, but is generally 1330 to 1410 ° C. in the case of cast iron, and generally 700 to 750 ° C. in the case of aluminum. The case is generally 1450-1500 ° C. In particular, the disappearance model casting method of the present embodiment can further reduce residual defects generated in the cast iron system.

  When castings are produced using the vanishing model coating composition, castings with few residual defects and seizure defects and a beautiful casting surface are obtained, so a complex structure and a beautiful casting surface are required. It is suitable for what is used. Specific examples of castings include members, parts, and the like used for automobile dies, machine tools, hydraulic valves for construction machines, motors, engine frames, building members, and the like.

  In relation to the above-described embodiment, the present invention further discloses the following composition, production method, or application.

<1> A vanishing model coating composition containing a refractory aggregate and amorphous cellulose.

<2> The average particle size of the refractory aggregate is preferably 20 μm or more, more preferably 40 μm or more, further preferably 50 μm or more, preferably 400 μm or less, more preferably 200 μm or less, still more preferably 150 μm or less, and further preferably 20 to 400 μm. The disappearing model coating composition according to <1>, wherein 40 to 200 μm is more preferable, and 50 to 150 μm is more preferable.
<3> The content of the refractory aggregate is preferably 30% by mass or more, more preferably 40% by mass or more, preferably 80% by mass or less, more preferably 70% by mass or less, and preferably 30 to 80% by mass, The coating agent composition for disappearance model according to <1> or <2>, wherein 40 to 70% by mass is more preferable.
<4> The degree of crystallinity of the non-crystalline cellulose is preferably 30% or less, more preferably 25% or less, still more preferably 20% or less, preferably -30% or more, more preferably -20% or more, -10 % Or more is more preferable, −30% to 30% is preferable, −20% to 25% is more preferable, and −10% to 20% is more preferable, and the disappearance model according to any one of the above items <1> to <3> Coating agent composition.
<5> The vanishing model coating composition according to any one of <1> to <4>, wherein the amorphous cellulose is preferably in the form of fibers and / or particles, and more preferably in the form of particles.
<6> The average particle diameter of the amorphous cellulose is preferably 50 μm or more, more preferably 80 μm or more, preferably 500 μm or less, more preferably 200 μm or less, preferably 50 to 500 μm, and more preferably 80 to 200 μm. 5> The coating agent composition for disappearance models.
<7> The fiber length of the amorphous cellulose is preferably 50 μm or more, more preferably 80 μm or more, further preferably 120 μm or more, preferably 600 μm or less, more preferably 300 μm or less, more preferably 50 to 600 μm, and preferably 80 to 300 μm. Is more preferable, 120-300 micrometers is still more preferable The coating agent composition for disappearance models as described in said <5>.
<8> The fiber diameter of the amorphous cellulose is preferably 10 μm or more, more preferably 20 μm or more, preferably 80 μm or less, preferably 10 to 80 μm, and more preferably 20 to 80 μm. <5> or <7> The disappearance model coating composition as described.
<9> The content of the amorphous cellulose is preferably 1 part by mass or more, more preferably 3 parts by mass or more, still more preferably 4 parts by mass or more, and 12 parts by mass or less with respect to 100 parts by mass of the refractory aggregate. Preferably, 10 parts by mass or less, more preferably 7 parts by mass or less, further preferably 1 to 12 parts by mass, more preferably 3 to 10 parts by mass, and still more preferably 4 to 7 parts by mass. 8> The disappearance model coating composition according to any one of the above.
<10> The vanishing model coating composition according to any one of <1> to <9>, further comprising a dispersant, wherein the dispersant does not dissolve the amorphous cellulose.
<11> The coating agent composition for disappearance model according to <10>, wherein the dispersion medium is preferably a lower alcohol, and more preferably ethanol.
<12> The content of the dispersion medium is preferably 20 parts by mass or more, more preferably 70 parts by mass or more, preferably 120 parts by mass or less, more preferably 110 parts by mass or less, with respect to 100 parts by mass of the refractory aggregate. 20-120 mass parts is preferable, 70-110 mass parts is more preferable The coating agent composition for disappearance models as described in said <11>.
<13> The vanishing model coating agent composition according to <10>, wherein the dispersion medium is preferably water.
<14> The dispersion medium is preferably 20 parts by mass or more, more preferably 70 parts by mass or more, preferably 150 parts by mass or less, more preferably 130 parts by mass or less, with respect to 100 parts by mass of the refractory aggregate. The disappearance model coating composition according to <13>, wherein the mass part is preferable, and 70 to 130 parts by mass is more preferable.
<15> Further, it contains a binder, and the content of the binder is preferably 0.5 parts by mass or more, preferably 30 parts by mass or less, and 100 to 100 parts by mass of the refractory aggregate. The disappearing model coating composition according to any one of <1> to <14>, wherein 30 parts by mass is preferable.
<16> Further, a sintering agent is contained, and the addition amount of the sintering agent is preferably 0.5 parts by mass or more, more preferably 1.0 part by mass or more, with respect to 100 parts by mass of the fireproof aggregate. Part or less, preferably 15 parts by weight or less, more preferably 0.5 to 30 parts by weight, and even more preferably 1.0 to 15 parts by weight for the disappearance model according to any one of the above items <1> to <15>. Coating agent composition.
<17> The vanishing model coating agent composition according to <16>, wherein the sintering agent is preferably calcium bentonite.
<18> A method for producing a casting disappearance model having a coating film around the disappearance model, wherein the disappearance model coating composition according to any one of <1> to <17> is used. A method for producing a disappearance model for castings, comprising a step of forming a coating film by adhering to the periphery.
<19> The method for producing a disappearance model for castings according to <18>, wherein the disappearance model is preferably foamed polystyrene.
<20> A casting manufacturing method using the casting disappearance model obtained by the casting disappearance model manufacturing method according to <18> or <19>, wherein the casting disappearance model is embedded in foundry sand. The manufacturing method of a casting which has a process and the process of casting a molten metal in the said disappearance model for castings embed | buried in the said foundry sand.
<21> A casting manufacturing method using the casting disappearance model obtained by the casting disappearance model manufacturing method according to any one of <18> or <19>, wherein the binder and the binder are added to the casting sand. A step of adding a curing agent that cures and preparing a mixture by kneading, a step of embedding the disappearance model for casting in the mixture, a step of casting molten metal into the disappearance model for casting embedded in the mixture, A method for producing a casting, comprising:
<22> Use of the coating composition for disappearance model according to any one of <1> to <17> as a coating agent for the disappearance model.

  Examples and the like specifically showing the present invention will be described below.

<Evaluation method>

[Cellulose type I crystallinity]
Cellulose type I crystallinity was calculated based on the above formula by measuring the X-ray diffraction intensity of the sample under the following conditions using a trade name “Rigaku RINT 2500VC X-RAY diffractometer” manufactured by Rigaku Corporation. . In addition, the sample for a measurement produced by compressing the pellet of area 320mm < ² > x thickness 1mm.
・ X-ray source: Cu / Kα-radiation
Tube voltage: 40 kv Tube current: 120 mA
Measurement range: Diffraction angle 2θ = 5-45 ° Scan speed: 10 ° / min

[TG decomposition start temperature]
Using “TG-8110” manufactured by Rigaku Corporation, the measurement was performed under the conditions of alumina pan φ5 mm × 2.5 H, AIR flow 500 ml / min, and heating rate 5 ° C./min. The temperature at the start of TG reduction was taken as the decomposition start temperature.

[Average particle size]
An average particle diameter is an average particle diameter of 50% of volume accumulation measured using the laser diffraction type particle size distribution measuring apparatus (LA-920 by Horiba, Ltd.). The analysis conditions are as follows.
・ Measurement method: Flow method ・ Dispersion medium: Ion exchange water ・ Dispersion method: Stirring, built-in ultrasonic wave 3 minutes ・ Sample concentration: 2 mg / 100 cc

[Method for evaluating residual defects]
The disappearance model 1 having the shape shown in FIG. 1 was prepared using expanded polystyrene (expanding ratio 50 times). A coating composition to be described later was adhered to the periphery of the disappearance model (dry film thickness: 1.4 mm) to prepare a disappearance model for casting. And 0.2 mass part of organic sulfonic-acid hardening | curing agents (the Kao Quaker make, C-14) are added to 100 mass parts of Fremantle quartz sand (No. 5), these are knead | mixed, Then, furan resin (the Kao Quaker make, EF) -5302) was mixed with 0.5 parts by mass with respect to 100 parts by mass of the silica sand. The above-mentioned disappearance model for casting is embedded in the obtained kneaded sand and cast from the weir at a speed that does not overflow the molten metal (cast iron: FC-250, casting temperature: 1400 ° C.). After 24 hours, the mold is released. The casting was taken out. About the obtained casting, the residual area (%) which generate | occur | produced on two 400 * 100 side surfaces of TP side surface was measured by image analysis.

[400 ° C air permeability evaluation method]
About the coating agent shown in Table 1 below, after the test piece is completed, it is heated in an oven that can be maintained at 400 ° C. ± 10 ° C. for 30 minutes and cooled to room temperature. The air permeability was measured according to “5. Air permeability test method” of “Test method of casting mold agent (March 1996)”. “400 ° C. air permeability change (6/60 min ratio)” is the measurement of the air permeability after 6 minutes and 60 minutes in an oven that can be maintained at 400 ° C. ± 10 ° C., and after 6 minutes / 60 minutes. It calculated in back x100. That is, it is an index indicating the air permeability at the initial stage of heating. A larger value indicates higher air permeability at the initial stage of heating.

[Solid content 65% viscosity]
About the coating agent shown in following Table 1, ion-exchange water was added and it adjusted so that it might become 65% of solid content. Thereafter, the viscosity (mPa · s) after a history of 60 seconds was measured with a rheometer under the conditions of (condition: parallel cone, 20 ° C., clearance 1 mm) at a shear rate of 10 s ⁻¹ .

[1000 ° C coating strength]
Regarding the coating agents shown in Table 1, according to “6. Fracture strength measurement method” of “Testing method for disappearance model casting coating agent (March 1996)” issued by Kansai branch of Japan Foundry Engineering Society. The film strength was measured. In addition, about 1000 degreeC heat processing, in order to set it as non-oxidizing atmosphere, the scaly graphite with an average particle diameter of 60 micrometers was filled in the crucible of (PHI) 50, and the test piece was embed | buried in the inside. Thereafter, the sample was heated for 1 hour in a muffle furnace capable of being maintained at 1000 ° C. ± 30 ° C., cooled to room temperature, and measured. In addition, it measured according to "6. Folding force measuring method" except a heating process.

<Production of amorphous cellulose>
As a cellulose-containing raw material, a sheet-like wood pulp (“HV-10” manufactured by Tenbeck Co., Ltd.) was cut through a sheet pelletizer (“SG (E) -220” manufactured by Horai Co., Ltd.). The obtained pulp was dried using shelf drying (manufactured by Advantech Co., Ltd., vacuum constant temperature dryer “DRV320DA”) so that the pulp after drying was 1.0% by mass. The pulp obtained by the drying process was put into a batch type vibration mill (manufactured by Chuo Kako Co., Ltd., “MB-1”), and the processing time was adjusted to produce spherical samples having different crystallinity. The sample was sieved to obtain amorphous cellulose having an average particle size shown in Table 1. Incidentally, the crystallinity of 17% was processed for 10 minutes, 4% for 20 minutes, and -15% for 30 minutes. For particle size adjustment, 28 mesh (aperture 589 μm) was sieved, and the amount passing through the sieve was collected. As for the coarse particles, 300 μm was further sieved with 100 mesh, and the sieve residue was collected. For 800 μm, a 28 mesh sieve residue was collected.

<Preparation of coating agent composition>
[Examples 1 to 9 and Comparative Examples 1 and 2]
Table 1 shows 100 parts by weight of refractory aggregate (silica (60% by mass, average particle size 80 μm), obsidian (20% by mass, average particle size 93 μm), graphite (20% by mass, average particle size 79 μm)). A nonionic surfactant (Kao Co., Ltd., Emulgen 106) 3.0 parts by weight, calcium bentonite 2.0 parts by weight, polyvinyl alcohol 2.0 parts by weight, and ion-exchanged water 40 parts by weight. Parts were mixed to prepare a coating composition. The unit of the addition amount described in Table 1 is part by mass. The concentration of the coating agent was determined by the following operation.

[Determination method of coating agent concentration]
A 300 × 150 (mm) expanded polystyrene model is set at the top at an elevation angle of 30 ° and a surface of 150 mm, and a half-round flow coating is performed. After drying at 50 ° C. for 1 hour, the same operation is applied twice and dried. The paint film was peeled off cleanly, four locations were measured with calipers, and the concentration was determined by adjusting the amount of water so that the average value was in the range of 1.4 mm ± 0.1.

Claims (8)

  A vanishing model coating composition containing a refractory aggregate and amorphous cellulose.   The disappearance model coating composition according to claim 1, wherein the crystallinity of the amorphous cellulose is 30% or less.   The vanishing model coating agent composition according to claim 1 or 2, wherein the amorphous cellulose is in the form of particles.   The vanishing model coating composition according to claim 3, wherein the amorphous cellulose has an average particle diameter of 50 to 500 μm.   The vanishing model coating composition according to any one of claims 1 to 4, wherein the content of the amorphous cellulose is 1 to 12 parts by mass with respect to 100 parts by mass of the refractory aggregate.   Furthermore, the coating agent composition for disappearance models according to any one of claims 1 to 5, further comprising a dispersant, wherein the dispersant does not dissolve the amorphous cellulose. A method for producing a casting disappearance model having a coating film around the disappearance model,
The manufacturing method of the disappearance model for casting which has the process of making the coating agent composition for disappearance models of any one of Claims 1-6 adhere to the circumference | surroundings of the said disappearance model, and forming a coating film. A casting manufacturing method using the casting disappearance model obtained by the casting disappearance model manufacturing method according to claim 7,
Burying the disappearance model for casting in foundry sand;
And a step of casting molten metal into the casting disappearance model embedded in the foundry sand.

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