Mold-forming binder composition

JP2026144272APending Publication Date: 2026-09-09KAO CORP
View PDF 1 Cites 0 Cited by

Patent Information

Application Number
JP2025031455
Authority / Receiving Office
JP · JP
Patent Type
Applications
Current Assignee / Owner
Filing Date
2025-02-28
Publication Date
2026-09-09

AI Technical Summary

Benefits of technology

【0008】 本発明によれば、低温(例えば5℃以下)環境下での鋳型造型用組成物の充填性の悪化を抑制することができ、かつ、鋳型強度を維持できる鋳型造型用粘結剤組成物、及びそれを含有する鋳型造型用組成物を提供することができる。

✦ Generated by Eureka AI based on patent content.

Smart Images

  • Figure 2026144272000001
    Figure 2026144272000001
  • Figure 2026144272000002
    Figure 2026144272000002
  • Figure 2026144272000003
    Figure 2026144272000003
Patent Text Reader

Abstract

To provide a mold-forming binder composition that can suppress deterioration of the filling properties of the mold-forming composition in a low-temperature environment (e.g., below 5°C) and maintain mold strength. [Solution] It contains alkali phenol resin and cardanol, A mold-forming binder composition wherein the mass ratio of the alkali phenol resin to the cardanol (mass of cardanol / mass of alkali phenol resin) is 0.01 to 0.40.
Need to check novelty before this filing date? Find Prior Art

Description

Technical Field

[0001] The present invention relates to a binder composition for mold making.

Background Art

[0002] A mold making method is known in which a phenol resin is used as a binder and the phenol resin is cured with an organic ester, carbon dioxide gas or amine gas (for example, Patent Document 1).

Prior Art Documents

Patent Documents

[0003]

Patent Document 1

Summary of the Invention

Problem to be Solved by the Invention

[0004] Binders containing an alkaline phenol resin experience increased viscosity under low temperature environments (e.g., 5°C or lower), which leads to problems such as deteriorated fluidity and fillability into molds of the mold-making composition containing the binder and refractory particles. When the fillability of the mold-making composition is poor, unevenness may occur on the surface of the obtained mold, or the surface strength of the mold may decrease, and casting defects such as sand inclusion, burning-on, penetration and veining may occur in the obtained casting.

[0005] To solve the above problem, adding a large amount of a solvent such as water is conceivable, but increasing the amount of solvent reduces the solid content of the binder, which may lead to decreased mold strength.

[0006] The present invention provides a binder composition for mold making that can suppress deterioration of fillability of a mold-making composition under low temperature environments (e.g., 5°C or lower) and maintain mold strength, and a mold-making composition containing the same.

Means for Solving the Problem

[0007] The present invention It contains alkali phenol resin and cardanol, This is a mold-forming binder composition in which the mass ratio of the alkali phenol resin to the cardanol (mass of cardanol / mass of alkali phenol resin) is 0.01 to 0.40. [Effects of the Invention]

[0008] According to the present invention, it is possible to provide a mold-forming binder composition that can suppress deterioration of the filling properties of a mold-forming composition in a low-temperature environment (e.g., 5°C or below) and maintain mold strength, and a mold-forming composition containing the same. [Modes for carrying out the invention]

[0009] <Bonding agent composition for mold making> The mold-forming binder composition of this embodiment (hereinafter also simply referred to as the binder composition) is It contains alkali phenol resin and cardanol, The mass ratio of the alkali phenol resin to the cardanol (mass of cardanol / mass of alkali phenol resin) is 0.01 to 0.40.

[0010] The binder composition of this embodiment can suppress the deterioration of the fillability of the mold-making composition in low-temperature environments (e.g., below 5°C) and maintain mold strength, and provides a binder composition that can do this. The reason why the binder composition of this embodiment exhibits such effects is not entirely clear, but it is thought to be as follows.

[0011] It is believed that the hydrophobic groups of the added cardanol are oriented at the gas-liquid interface, lowering the surface tension, and at the same time, they strongly interact with the alkali-phenol resin through π-π stacking, reducing intermolecular friction, thereby suppressing the deterioration of the filler properties of the mold-making composition at low temperatures.

[0012] [Alkali phenolic resin] The aforementioned alkali-phenol resin is generally obtained by polycondensation of a phenol compound and an aldehyde compound under alkaline conditions. The phenol compound can be a mixture of one or more of various phenol compounds, including phenol, bisphenol A, bisphenol F, cresol, 3,5-xylenol, resorcinol, catechol, nonylphenol, p-tert-butylphenol, isopropenylphenol, phenylphenol, and other substituted phenols. The aldehyde compound can be a mixture of one or more of formaldehyde, acetaldehyde, furfural, glyoxal, etc. These compounds can be used as aqueous solutions as needed. Furthermore, monomers that can condense with aldehyde compounds, such as urea, melamine, and cyclohexanone, as well as monohydric aliphatic alcohol compounds such as methanol, ethanol, isopropyl alcohol, n-propyl alcohol, and butyl alcohol, and water-soluble polymers such as polyacrylates, cellulose derivative polymers, polyvinyl alcohol, and lignin derivatives may also be mixed with these. From the viewpoint of improving the filling properties of the mold-forming composition in low-temperature environments and suppressing the reduction in mold strength, preferably the phenol compound is 95 mol% or more, more preferably substantially 100 mol% or more, and even more preferably 100 mol%. In this specification, "substantially" means that an amount equivalent to an impurity may be present.

[0013] Examples of alkali catalysts used in the synthesis of the alkali-phenol resin include alkali metal hydroxides such as LiOH, NaOH, and KOH, with NaOH and / or KOH being particularly preferred. Alternatively, these alkali catalysts may be mixed with the binder composition. The alkali metal hydroxide is preferably used in an amount of 0.01 to 6 moles, more preferably 0.5 to 2.5 moles, per mole of phenol.

[0014] Generally, the alkali phenol resin is used in aqueous solution form. The alkali phenol resin content in the aqueous alkali phenol resin solution (solid mass after drying the aqueous alkali phenol resin solution at 105°C for 3 hours) is preferably 30% by mass or more, and more preferably 50% by mass or more, from the viewpoint of improving mold strength. The alkali phenol resin content in the aqueous alkali phenol resin solution is preferably 85% by mass or less, and more preferably 75% by mass or less, from the viewpoint of improving mold strength and workability. Furthermore, the alkali phenol resin content in the aqueous alkali phenol resin solution is preferably 30 to 85% by mass, and more preferably 50 to 75% by mass, from the viewpoint of improving mold strength and workability.

[0015] The weight-average molecular weight (Mw) of the alkali phenol resin is preferably 500 or more, more preferably 800 or more, and even more preferably 1200 or more, from the viewpoint of improving mold strength. The weight-average molecular weight (Mw) of the alkali phenol resin is preferably 8000 or less, more preferably 5000 or less, and even more preferably 3000 or less, from the viewpoint of improving mold strength and workability. Furthermore, the weight-average molecular weight (Mw) of the alkali phenol resin is preferably 500 to 8000, more preferably 800 to 5000, and even more preferably 1200 to 3000, from the viewpoint of improving mold strength and workability. The weight-average molecular weight of the alkali phenol resin is measured by the method described in the examples.

[0016] From the viewpoint of improving mold strength, the content of the alkali phenol resin in the binder composition is preferably 10% by mass or more, more preferably 20% by mass or more, even more preferably 25% by mass or more, and even more preferably 30% by mass or more. From the viewpoint of suppressing thickening of the binder composition during storage and improving the fluidity of the mold-making composition, the content of the alkali phenol resin in the binder composition is preferably 70% by mass or less, more preferably 60% by mass or less, even more preferably 55% by mass or less, and even more preferably 50% by mass or less. Furthermore, from the viewpoint of improving mold strength, suppressing thickening of the binder composition during storage and improving the fluidity of the mold-making composition, the content of the alkali phenol resin in the binder composition is preferably 10 to 70% by mass, more preferably 20 to 60% by mass, even more preferably 25 to 60% by mass, even more preferably 30 to 60% by mass, even more preferably 30 to 55% by mass, and even more preferably 30 to 50% by mass.

[0017] [Cardanol] Cardanol is a component found in the shell of cashew nuts and is a compound represented by the following general formula (1). [ka] (In the above general formula (1), R is -(CH2) 14 CH3, -(CH2)6CH=CH(CH2)6CH3, -(CH2)6CH=CHCH2CH=CH(CH2)3CH3, or -(CH2)6CH=CHCH2CH=CH(CH2)2CH=CH2.

[0018] From the viewpoints of improving the fillability of the composition for mold making under low-temperature environment and suppressing a decrease in mold strength, the content of said cardanol in said binder composition is preferably 1% by mass or more, more preferably 3% by mass or more, still more preferably 5% by mass or more, and even more preferably 7% by mass or more. From the viewpoint of suppressing a decrease in mold strength, the content of said cardanol in said binder composition is preferably 20% by mass or less, more preferably 15% by mass or less, still more preferably 13% by mass or less, and even more preferably 10% by mass or less. Furthermore, from the viewpoints of suppressing an increase in viscosity of the composition for mold making under low-temperature environment to improve fluidity and suppressing a decrease in mold strength, the content of said cardanol in said binder composition is preferably 1 to 20% by mass, more preferably 3 to 15% by mass, still more preferably 5 to 13% by mass, and even more preferably 7 to 10% by mass.

[0019] From the viewpoints of improving the fillability of the composition for mold making under low-temperature environment and suppressing a decrease in mold strength, the mass ratio of said alkali phenol resin to said cardanol (mass of said cardanol / mass of said alkali phenol resin) is 0.01 or more, preferably 0.05 or more, more preferably 0.10 or more, still more preferably 0.15 or more, even more preferably 0.20 or more, and still further more preferably 0.25 or more. From the viewpoint of suppressing a decrease in mold strength, the mass ratio of said alkali phenol resin to said cardanol is 0.40 or less, preferably 0.38 or less, and more preferably 0.35 or less. Furthermore, from the viewpoints of improving the fillability of the composition for mold making under low-temperature environment and suppressing a decrease in mold strength, the mass ratio of said alkali phenol resin to said cardanol is 0.01 to 0.40, preferably 0.05 to 0.40, more preferably 0.10 to 0.38, still more preferably 0.15 to 0.38, even more preferably 0.20 to 0.35, and still further more preferably 0.25 to 0.35.

[0020] [Water] The binder composition may further contain water. From the viewpoints of suppressing thickening of the binder composition during storage and improving the fluidity of the mold making composition, the content of water in the binder composition is preferably 10% by mass or more, more preferably 20% by mass or more, and still more preferably 25% by mass or more. From the viewpoints of improving mold strength, suppressing thickening of the binder composition during storage, and improving the fluidity of the mold making composition, the content of water in the binder composition is preferably 60% by mass or less, more preferably 50% by mass or less, still more preferably 45% by mass or less, and even more preferably 40% by mass or less. Further, from the viewpoints of suppressing thickening of the binder composition during storage, improving the fluidity of the mold making composition, and improving mold strength, the content of water in the binder composition is preferably 10 to 60% by mass, more preferably 20 to 50% by mass, still more preferably 25 to 45% by mass, and even more preferably 25 to 40% by mass.

[0021] The mass ratio of the alkaline phenol resin to water in the binder composition (mass of water / mass of alkaline phenol resin) is preferably 0.3 or more, more preferably 0.4 or more, and still more preferably 0.5 or more, from the viewpoints of suppressing thickening of the binder composition during storage and improving the fluidity of the mold making composition. From the viewpoints of improving mold strength, suppressing thickening of the binder composition during storage, and improving the fluidity of the mold making composition, the mass ratio of the alkaline phenol resin to water in the binder composition is preferably 1.5 or less, more preferably 1.3 or less, and still more preferably 1.2 or less. Further, the mass ratio of the alkaline phenol resin to water in the binder composition is preferably 0.3 to 1.5, more preferably 0.4 to 1.3, and still more preferably 0.5 to 1.2, from the viewpoints of suppressing thickening of the binder composition during storage, improving the fluidity of the mold making composition, and improving mold strength.

[0022] [Other Components] The binder composition may further contain additives such as silane coupling agents, aluminates, and oxyanion compounds, to an extent that does not hinder the effects of this embodiment.

[0023] [Silane coupling agent] The binder composition preferably contains a silane coupling agent from the viewpoint of improving mold strength. Examples of the silane coupling agent include γ-(2-amino)propylmethyldimethoxysilane, γ-aminopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, γ-glycidoxypropyltrimethoxysilane, and N-β-(aminoethyl)γ-aminopropylmethyldimethoxysilane. The content of the silane coupling agent in the binder composition is preferably 0.1 to 5% by mass, more preferably 0.3 to 1% by mass, from the viewpoint of improving mold strength.

[0024] [Aluminate] The binder composition preferably contains an aluminate from the viewpoint of improving mold strength. Examples of the aluminate include alkali metal salts of aluminic acid. From the viewpoint of improving mold strength, sodium aluminate is preferred. From the viewpoint of improving mold strength, the content of the aluminate in the binder composition is preferably 0.1% by mass or more, more preferably 0.5% by mass or more, and even more preferably 1% by mass or more. From the viewpoint of improving mold strength, the content of the aluminate in the binder composition is preferably 10% by mass or less, more preferably 5% by mass or less, and even more preferably 3% by mass or less. Furthermore, from the viewpoint of improving mold strength, the content of the aluminate in the binder composition is preferably 0.1 to 10% by mass, more preferably 0.5 to 5% by mass, and even more preferably 1 to 3% by mass.

[0025] [Oxyanionic compounds] When curing the binder composition with carbon dioxide, it is preferable to include an oxyanion compound from the viewpoint of improving mold strength and improving the curing speed of the mold. This is because it is thought that the oxyanion compound forms an ionomer and polymerizes the alkali phenol resin only after absorbing carbon dioxide. Examples of the oxyanion compound include boric acid and borate compounds. Examples of borates include sodium tetraborate decahydrate (borax), potassium tetraborate decahydrate, sodium metaborate, sodium pentaborate, and potassium pentaborate. From the viewpoint of improving mold strength and improving the curing speed of the mold, sodium tetraborate decahydrate (borax) is preferred.

[0026] The content of the oxyanion compound in the binder composition is preferably 1% by mass or more, more preferably 3% by mass or more, even more preferably 5% by mass or more, and even more preferably 6% by mass or more, from the viewpoint of improving mold strength and improving the curing speed of the mold. The content of the oxyanion compound in the binder composition is preferably 30% by mass or less, more preferably 20% by mass or less, even more preferably 15% by mass or less, and even more preferably 10% by mass or less, from the viewpoint of improving mold strength and improving the fluidity of the mold-making composition. Furthermore, the content of the oxyanion compound in the binder composition is preferably 1 to 30% by mass, more preferably 3 to 20% by mass, even more preferably 5 to 15% by mass, and even more preferably 6 to 10% by mass, from the viewpoint of improving mold strength, improving the curing speed of the mold and improving the fluidity of the mold-making composition.

[0027] <Method for manufacturing molds> In the mold manufacturing method of this embodiment, the mold can be manufactured by using the conventional mold manufacturing process as is. A preferred mold manufacturing method includes a mixing step of mixing at least refractory particles and the binder composition to obtain a mold-forming composition, and a curing step of filling the mold-forming composition into a mold and curing the mold-forming composition.

[0028] [Mixing process] [Fire-resistant particles] The refractory particles usable in the mold manufacturing method of this embodiment include conventionally known materials such as silica sand, chromite sand, zircon sand, olivine sand, alumina sand, mullite sand, synthetic mullite sand, and alumina ball sand. Recycled sand obtained by recovering and recycling used refractory particles can also be used. The refractory particles can be used individually or in combination of two or more types.

[0029] The average particle size of the refractory particles is preferably greater than 50 μm, more preferably 70 μm or more, even more preferably 120 μm or more, and even more preferably 150 μm or more, from the viewpoint of improving mold strength and economic efficiency. From the same viewpoint, it is preferably 600 μm or less, more preferably 400 μm or less, even more preferably 300 μm or less, and even more preferably 250 μm or less. In this specification, the average particle size is measured by the method described in the examples.

[0030] In the aforementioned mixing process, known methods can be used to mix each raw material. For example, methods include adding and kneading each raw material using a batch mixer, or supplying each raw material to a continuous mixer and kneading it.

[0031] The ratio of the refractory particles to the binder composition can be set as appropriate, but from the viewpoint of improving mold strength and economic efficiency, the content of the binder composition per 1000 parts by mass of the refractory particles is preferably 5 parts by mass or more, more preferably 10 parts by mass or more, preferably 100 parts by mass or less, more preferably 80 parts by mass or less, even more preferably 50 parts by mass or less, and even more preferably 40 parts by mass or less. Furthermore, the alkali phenol resin per 1000 parts by mass of the refractory particles is preferably 3 parts by mass or more, more preferably 5 parts by mass or more, preferably 80 parts by mass or less, even more preferably 50 parts by mass or less, even more preferably 30 parts by mass or less, and even more preferably 25 parts by mass or less.

[0032] Furthermore, a mold-making composition can be obtained by mixing refractory particles, an aqueous alkali phenol resin solution, a binder composition that does not contain cardanol, and cardanol. In this case, the amount of cardanol used is the same as the amount described in the binder composition.

[0033] Furthermore, a mold-making composition can also be obtained by separately mixing the refractory particles, the aqueous alkali phenol resin solution, the cardanol, and other components used in the binder composition. In this case, the alkali phenol resin content is preferably 3 parts by mass or more, and preferably 80 parts by mass or less, per 1000 parts by mass of refractory particles. The amounts of the cardanol and other components used in the binder composition are the same as those described in the binder composition.

[0034] When the cardanol is mixed separately from the binder composition as described above, the cardanol is a mold-making additive. The mold-making additive of this embodiment contains the cardanol. The preferred embodiment of the cardanol in the mold-making additive of the present invention is the same as the preferred embodiment of the cardanol in the binder composition.

[0035] [Curing process] In the curing step, the mold-forming composition is packed into a mold and cured. A commonly known method can be used to cure the mold-forming composition. One method for curing the mold-forming composition is curing it with a curing agent. Examples of curing agents include organic ester compounds and carbon dioxide.

[0036] As the aforementioned organic ester compounds, lactones having 3 to 10 carbon atoms, organic esters derived from monohydric or polyhydric alcohols having 1 to 10 carbon atoms and organic carboxylic acids having 1 to 10 carbon atoms, or alkylene carbonates having 1 to 8 carbon atoms can be used alone or in combination. In the self-hardening mold molding method, it is preferable to use γ-butyrolactone, propionactone, ε-caprolactone, ethyl formate, ethylene glycol diacetate, ethylene glycol monoacetate, triacetin, ethylene carbonate, propylene carbonate, etc.

[0037] When an organic ester is used as the curing agent, the amount of the organic ester is preferably 10 parts by mass or more, more preferably 15 parts by mass or more, and more preferably 35 parts by mass or less, and more preferably 30 parts by mass or less, per 100 parts by mass of the binder composition, from the viewpoint of improving mold strength, improving curing speed, and economic efficiency.

[0038] When an organic ester is used as the curing agent, the amount of organic ester is preferably 20 parts by mass or more, more preferably 30 parts by mass or more, and more preferably 70 parts by mass or less, and more preferably 60 parts by mass or less, per 100 parts by mass of phenolic resin, from the viewpoint of improving mold strength, improving curing speed, and economic efficiency.

[0039] When carbon dioxide is used as the curing agent, the flow rate of the carbon dioxide should be such that, from the viewpoint of improving the strength of the mold, the mold is 100 cm 3 The flow rate is preferably 0.2 L / min or more, more preferably 1 L / min or more, even more preferably 5 L / min or more, even more preferably 10 L / min or more, and even more preferably 15 L / min or more, and from the viewpoint of economy, a mold of 100 cm 3The flow rate is preferably 30 L / min or less, more preferably 25 L / min or less. The carbon dioxide flow time is preferably 10 seconds or more, more preferably 20 seconds or more, and even more preferably 25 seconds or more, from the viewpoint of improving mold strength, and preferably 90 seconds or less, more preferably 70 seconds or less, even more preferably 50 seconds or less, and even more preferably 40 seconds or less, from the viewpoint of economic efficiency. The curing temperature is preferably -5°C or higher, more preferably 5°C or higher, and even more preferably 10°C or higher, from the viewpoint of improving mold strength, and preferably 45°C or lower, more preferably 40°C or lower, and even more preferably 35°C or lower, from the viewpoint of economic efficiency.

[0040] When carbon dioxide is used as the curing agent, the amount of carbon dioxide is preferably 25 parts by mass or more, more preferably 30 parts by mass or more, and preferably 100 parts by mass or less, and more preferably 75 parts by mass or less, per 100 parts by mass of the binder composition, from the viewpoint of improving mold strength, improving curing speed, and economic efficiency.

[0041] When carbon dioxide is used as the curing agent, the amount of carbon dioxide is preferably 50 parts by mass or more, more preferably 60 parts by mass or more, and more preferably 200 parts by mass or less, and more preferably 150 parts by mass or less, per 100 parts by mass of alkali phenolic resin, from the viewpoint of improving mold strength, improving curing speed, and economic efficiency.

[0042] <Mold making composition> The mold-making composition of this embodiment contains the refractory particles and the binder composition. That is, the mold-making composition of this embodiment contains the refractory particles, the alkali phenol resin and the cardanol.

[0043] The content of the binder composition is as described in the mixing step of the mold manufacturing method with respect to the refractory particles.

[0044] The content of the alkali phenol resin is as described in the mixing step of the mold manufacturing method with respect to the refractory particles. The content of the cardanol is as described in the binder composition with respect to the alkali phenol resin. [Examples]

[0045] The following describes specific examples illustrating the present invention.

[0046] <Method for evaluating raw materials> [Weight-average molecular weight (Mw) of alkali phenolic resin] The weight-average molecular weight (Mw) of the alkali phenol resin was measured by GPC (gel permeation chromatography) under the following conditions. (a) Sample preparation: An equal weight of deionized water was added to the sample, and neutralization was performed by adding 0.1% by mass of H2SO4. The resulting precipitate was filtered, washed with water, and dried. This was dissolved in tetrahydrofuran (THF) to prepare the sample for GPC. (b) Columns: One Guard Column TSX (manufactured by Toyo Soda Industries Co., Ltd.) HXL (6.5 mmφ × 4 cm), one TSK3000HXL (7.8 mmφ × 30 cm), and one TSK2500HXL (7.8 mmφ × 30 cm) were used. The columns were connected in the order of Guard Column TSX HXL - TSK3000HXL - TSK2500HXL from the injection port side. (c) Standard material: Monodisperse polystyrene with known weight-average molecular weight (manufactured by Toyo Soda Co., Ltd.) (d) Eluent: THF (flow rate: 1cm 3 / min) (e) Column temperature: 25℃ (f) Detector: Ultraviolet spectrophotometer (quantification at the wavelength of the maximum peak of ultraviolet absorption of phenol) (g) Splitting method for molecular weight calculation: Time splitting (2 sec)

[0047] [Average particle size] (For particles larger than 53 μm) Based on the method specified in Annex 2 of JIS Z2601 (1993) "Test Methods for Foundry Sand," measurements were taken using sieves of 850, 600, 425, 300, 212, 150, 106, 75, and 53 μm, and the particle size at 50% mass accumulation was taken as the average particle size. (For particles smaller than 53 μm) This is the average particle diameter at 50% volume cumulative, measured using a laser diffraction particle size distribution analyzer (LA-920, Horiba, Ltd.). The analysis conditions are as follows: • Measurement method: Flow method • Dispersion medium: Ion-exchanged water • Dispersion method: stirring, built-in ultrasonic for 3 minutes • Sample concentration: 2 mg / 100 cc

[0048] <Preparation of alkaline phenolic resin aqueous solution> In a 2-liter glass container equipped with a thermometer and stirrer, 344.0 g of phenol, 128.3 g of 48% potassium hydroxide aqueous solution, 242.4 g of water, and 238.7 g of 92% paraformaldehyde were mixed and reacted at 80°C to obtain an alkaline phenol resin aqueous solution. The alkali phenol resin content (solid content concentration) in the alkaline phenol resin aqueous solution was 65.6% by mass. The weight-average molecular weight (Mw) of the alkali phenol resin was 2176.

[0049] <Examples and Comparative Examples> [Example 1 (Preparation of binder composition)] A binder composition according to Example 1 was obtained using 51.0% by mass of the alkali phenol resin aqueous solution (33.4% by mass of alkali phenol resin), 2.0% by mass of cardanol, 26.4% by mass of a 48% by mass potassium hydroxide aqueous solution, 10.5% by mass of triethylene glycol monoethyl ether, 2.9% by mass of a 50% by mass sodium aluminate aqueous solution, 6.5% by mass of sodium tetraborate decahydrate (borax), and 0.7% by mass of 3-glycidoxypropyltrimethoxysilane (KBM-403, manufactured by Shin-Etsu Chemical Co., Ltd.) as a silane coupling agent. The composition of the obtained binder composition is shown in Table 1.

[0050] [Examples 2-4 (Preparation of binder composition)] Except for changing the mass percentages of the alkali phenol resin aqueous solution and cardanol, the same procedure as in Example 1 was followed to obtain the binder compositions according to Examples 2 to 4. The compositions of the obtained binder compositions are shown in Table 1.

[0051] [Example 5 (Preparation of binder composition)] A binder composition according to Example 5 was obtained using 64.5% by mass of the alkali phenol resin aqueous solution (42.3% by mass of alkali phenol resin), 3.0% by mass of cardanol, 9.2% by mass of a 48% by mass sodium hydroxide aqueous solution, 22.3% by mass of water, 0.2% by mass of a 50% by mass sodium aluminate aqueous solution, and 0.8% by mass of 3-glycidoxypropyltrimethoxysilane (KBM-403, manufactured by Shin-Etsu Chemical Co., Ltd.) as a silane coupling agent. The composition of the obtained binder composition is shown in Table 2.

[0052] [Comparative Examples 1 and 2 (Preparation of Binding Agent Compositions)] The procedure was carried out in the same manner as in Example 1, except that the mass percentages of the alkali phenol resin aqueous solution and cardanol were changed, to obtain the binder compositions for Comparative Examples 1 and 2. The compositions of the obtained binder compositions are shown in Table 1.

[0053] [Comparative Example 3 (Preparation of Binding Agent Composition)] The procedure was carried out in the same manner as in Example 5, except that the mass percentages of the alkali phenol resin aqueous solution and cardanol were changed, to obtain the binder composition according to Comparative Example 3. The composition of the obtained binder composition is shown in Table 2.

[0054] <Evaluation Method> [Examples 1-4, Comparative Examples 1 and 2] [Evaluation of filling properties] Under conditions of 5°C and 55% RH, 1000 parts by mass of refractory particles cooled to 5°C and 30 parts by mass of the binder composition were added to a kitchen mixer "Kenmix Aiko Chef" (manufactured by Aikosha Seisakusho Co., Ltd.) equipped with an aluminum beater stirring blade. The mixture was mixed at a rotation speed of 300 rpm for 2 minutes to obtain a mold-making composition. The obtained mold-making composition was filled into a 50 mmΦ × 300 mm test tube from the top to the top end, and the mass was measured. A larger mass indicates better filling performance. The refractory particles used were silica sand ("Mikawa Silica Sand R Grade No. 6," manufactured by Mikawa Silica Co., Ltd.). The average particle size of the refractory particles was 181 μm. The evaluation results are shown in Table 1.

[0055] [Evaluation of mold strength] Under conditions of 5°C and 55%RH, 1000 parts by mass of refractory particles cooled to 5°C and 30 parts by mass of the binder composition were added to a kitchen mixer "Kenmix Aiko Chef" (manufactured by Aikosha Seisakusho Co., Ltd.) equipped with an aluminum beater stirring blade, and mixed at a rotation speed of 300 rpm for 2 minutes to obtain a mold-making composition. The obtained mold-making composition was filled into a wooden mold for a test piece measuring 50 mmΦ × 50 mm, and carbon dioxide gas was passed through it at a flow rate of 20 L / min at 25°C for 30 seconds to obtain an evaluation test piece. After 30 seconds had elapsed since carbon dioxide gas passage, the mold compressive strength of the test piece was measured using a compressive strength evaluation tester ("SDW-020F" manufactured by Imada Seisakusho Co., Ltd.) at a speed of 5 mm / min. The evaluation results are shown in Table 1.

[0056] [Example 5, Comparative Example 3] [Evaluation of filling properties] Under conditions of 5°C and 55% RH, 1000 parts by mass of refractory particles cooled to 5°C, 15 parts by mass of the binder composition, and 3.0 parts by mass of triacetin were added to a kitchen mixer "Kenmix Aiko Chef" (manufactured by Aikosha Seisakusho Co., Ltd.) equipped with an aluminum beater stirring blade. The mixture was then mixed at a rotation speed of 300 rpm for 2 minutes to obtain a mold-making composition. The obtained mold-making composition was filled into a 50 mmΦ × 300 mm test tube from the top to the top of the tube, and the mass was measured. A larger mass value indicates better filling performance. The refractory particles used were silica sand ("Mikawa Silica Sand R Grade No. 6," manufactured by Mikawa Silica Co., Ltd.). The average particle size of the refractory particles was 181 μm. The evaluation results are shown in Table 2.

[0057] [Evaluation of mold strength] Under conditions of 5°C and 55% RH, 1000 parts by mass of refractory particles cooled to 5°C, 15 parts by mass of the binder composition, and 3.0 parts by mass of triacetin were added to a kitchen mixer "Kenmix Aiko Chef" (manufactured by Aikosha Seisakusho Co., Ltd.) equipped with an aluminum beater stirring blade. The mixture was then mixed at a rotation speed of 300 rpm for 2 minutes to obtain a mold-making composition. The obtained mold-making composition was filled into a wooden mold for a test piece measuring 50 mmΦ × 50 mm, and left to stand at 25°C for 30 minutes to obtain an evaluation test piece. The test piece was evaluated using a compressive strength evaluation tester ("SDW-020F" manufactured by Imada Seisakusho Co., Ltd.) at a speed of 5 mm / min to measure the mold compressive strength of the test piece. The evaluation results are shown in Table 2.

[0058] [Table 1]

[0059] [Table 2]

Claims

1. It contains alkali phenol resin and cardanol, A mold-forming binder composition wherein the mass ratio of the alkali phenol resin to the cardanol (mass of cardanol / mass of alkali phenol resin) is 0.01 to 0.

40.

2. The aforementioned alkali phenol resin is obtained by polycondensing a phenol compound and an aldehyde compound under alkaline conditions. The mold-forming binder composition according to claim 1, wherein 95 mol% or more of the phenol compound is phenol.

3. The mold-forming binder composition according to claim 1, wherein the content of the alkali phenol resin in the mold-forming binder composition is 10% by mass or more and 70% by mass or less.

4. The mold-forming binder composition according to claim 1, wherein the cardanol content in the mold-forming binder composition is 1% by mass or more and 20% by mass or less.

5. The mold-forming binder composition according to claim 1, wherein it contains water and the mass ratio of the alkali phenol resin to the water (mass of water / mass of alkali phenol resin) is 0.3 to 1.

5.

6. A mold-making composition containing a mold-making binder composition and refractory particles according to any one of claims 1 to 5.

7. A method for manufacturing a mold, comprising a mixing step of mixing refractory particles and a mold-forming binder composition according to any one of claims 1 to 5 to obtain a mold-forming composition, and a curing step of filling a mold-forming composition into a mold and curing the mold-forming composition.

8. The method for producing a mold according to claim 7, wherein the curing agent used to cure the mold-making composition in the curing step is an organic ester compound or carbon dioxide.

9. A mold-making additive containing cardanol.

10. It contains fire-resistant particles, alkali phenol resin, and cardanol. A mold-making composition wherein the mass ratio of the alkali phenol resin to the cardanol (mass of cardanol / mass of alkali phenol resin) is 0.01 to 0.40.

Citation Information

Patent Citations

  • Organic binding agent for mold, and molding sand composition and mold obtained by using the same

    JP2006192477A