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JPS6124099B2 - - Google Patents
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JPS6124099B2 - - Google Patents

Info

Publication number
JPS6124099B2
JPS6124099B2 JP59107348A JP10734884A JPS6124099B2 JP S6124099 B2 JPS6124099 B2 JP S6124099B2 JP 59107348 A JP59107348 A JP 59107348A JP 10734884 A JP10734884 A JP 10734884A JP S6124099 B2 JPS6124099 B2 JP S6124099B2
Authority
JP
Japan
Prior art keywords
mold
material mixture
resin
mold material
curing
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP59107348A
Other languages
Japanese (ja)
Other versions
JPS60250853A (en
Inventor
Hideaki Oota
Naomi Hayashi
Shozo Fujii
Yasushi Sakaguchi
Mitsuo Ninomya
Kimisada Hori
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
National Institute of Advanced Industrial Science and Technology AIST
Original Assignee
Agency of Industrial Science and Technology
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology
Priority to JP10734884A priority Critical patent/JPS60250853A/en
Publication of JPS60250853A publication Critical patent/JPS60250853A/en
Publication of JPS6124099B2 publication Critical patent/JPS6124099B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22CFOUNDRY MOULDING
    • B22C9/00Moulds or cores; Moulding processes
    • B22C9/12Treating moulds or cores, e.g. drying, hardening

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Mold Materials And Core Materials (AREA)
  • Molds, Cores, And Manufacturing Methods Thereof (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は酸硬化性樹脂を粘結剤とし、強酸と弱
塩基物質から成る塩を硬化剤とした鋳型材混合物
を空気等の高温ガスで急速に硬化させる鋳型製造
法に関するものである。 一般に樹脂を粘結剤とした鋳型は、シエルモール
ド法のように、あらかじめ耐火性粒状物より成る
鋳物砂中に樹脂と触媒を加えておき、この鋳型材
混合物を金型を介して加熱硬化させたり、自硬性
鋳型法のように鋳物砂中に樹脂と常温で反応硬化
する触媒を加えておき、十分に反応時間を与えて
硬化させる方法等が採用されている。しかし前者
の方法は熱に耐える金型が必要であるため、高額
の型製造費がかかり非量産鋳物の製造には適用し
がたいことと、後者の方法は硬化を早くするため
には可使時間が短く、逆に可使時間を長くすると
硬化させるのに長時間を必要とし、生産性が悪い
という欠点がある。そのため、ガスの吹き込みに
よつて急速に硬化する方法の開発が要望されてい
る。 これまでのところ、ウレタン樹脂を粘結剤とし
た鋳型材をアミンガスの吹き込みで硬化させる方
法と、酸硬化性樹脂を粘結剤とし、さらにメチル
エチルケトンパーオキサイドのような過酸化物を
加えた鋳型材を亜硫酸ガスの吹き込みで硬化させ
る方法等が考案されている。しかるにアルミンガ
スや亜硫酸ガスは人体に有害であるために、使用
にあたつては作業場にガスが漏れないようにする
ことと、中和処理をして放出すること等が必要で
設備的負担が大きい。 本発明は有害ガスに代えて、空気等の無害なガ
スを高温にして使用するもので、特別な設備を必
要をしないほか、木型が使用でき、鋳型材混合物
の可使時間は十分にあり、鋳型の生産性もよいも
のである。 以下に本本発明を詳細に説明する。 本発明に使用する粘結剤はフラン樹脂、フエノ
ール樹脂等の酸硬化性樹脂で、今日自硬性鋳型に
使用されている酸硬化性樹脂はそのまま使用でき
る。硬化触媒は強酸と弱塩基物質から成る塩で、
例えば硫酸水素アンモニウムや過硫酸アンモニウ
ムを使用すると高温のガスで容易に分解し、弱塩
基物であるアンモニウムを放出して強酸を残し、
酸硬化性樹脂を急速に硬化させる。しかもこれら
の塩は酸硬化性樹脂と混ぜ合せても容易には分解
せず、鋳型材混合物として十分な可使時間があ
る。 従来より鋳型材混合物中の樹脂を高温のガスで
固める方法は種々試みられてきたが、従来のもの
は、酸硬化性樹脂に低濃度の酸を適用したり、弱
酸を適用して可使時間を長くし、昇温効果によつ
て反応を促進するか、比較的飛散しやすい有機機
溶剤を用いた樹脂を使用して、溶剤を飛散させて
硬化させる方法のいずれかであつて、高温ガスに
よる硬化性は十分でなかつた。 本発明は触媒として強酸と弱塩基物質から成る
塩を用い、鋳型材混合物で鋳型を造型した後高温
のガスの吹き込みによつて強酸に変え、急速に硬
化させるという新しい方式にもとずくもので、鋳
型材混合物の可使時間は十分に長く、高温のガス
による硬化性も従来の方式をはるかに凌駕するも
のである。 また大きな鋳型は、高温のガスの侵透が不十分
であつたり、鋳型中を通過する間に温度が低下
し、部分的に硬化性が悪い場合があるが、そのよ
うな場合、模型定盤にベントホールを設けて、鋳
型材砂粒子間の空気を吸引したり、模型定盤にバ
イブレータを取りつけるなどして、微振動を与
え、模型と鋳型材混合物間に微細な隙間を設けつ
つ高温のガスを吹き込めば硬化性を改善できる。 以下実施例により本発明を具体的に説明する。 〔実施例 1〕 硫酸水素アンモニウム100gと水100gを容器に
入れ、撹拌して濃度50%の硬化触媒を作成した。 次いでけい砂10Kgに硬化触媒50gを添加して約
30秒間混合したのち、フラン樹脂100gを添加し
て1分間混合し、鋳型材混合物を得た。ここで鋳
型材混合物を一定時間経過ごとに、直径50mm、高
さ50mmの空胴3ケを有する割型に充填し、その底
部に設けたベントホールから鋳型材混合物間の空
気を吸引しつつ、上部へ温風器により高温の空気
を約2分間に渡つて吸きつけた。ここで得られた
鋳型の通気直後の強度並びに翌日の強度を鋳型材
混合物を準備した後の経過時間との関係で示すと
次の通りである。
The present invention relates to a mold manufacturing method in which a mold material mixture using an acid-curing resin as a binder and a salt made of a strong acid and a weak base substance as a hardening agent is rapidly hardened with a high-temperature gas such as air. Generally, molds using resin as a binder are made by adding resin and catalyst to molding sand made of refractory granules in advance, and then heating and hardening this mold material mixture through a mold, as in the shell mold method. Alternatively, methods such as the self-hardening mold method, in which a catalyst that reacts with the resin and hardens at room temperature is added to the molding sand, and a sufficient reaction time is given to harden the resin, have been adopted. However, the former method requires a mold that can withstand heat, resulting in high mold manufacturing costs and is difficult to apply to manufacturing non-mass-produced castings. If the pot life is short and the pot life is long, it will take a long time to harden, resulting in poor productivity. Therefore, there is a demand for the development of a method for rapidly curing by blowing gas. So far, two methods have been developed: a mold material using urethane resin as a binder and curing by blowing amine gas, and a mold material using acid-curing resin as a binder and adding peroxide such as methyl ethyl ketone peroxide. A method of curing by blowing sulfur dioxide gas has been devised. However, since aluminous gas and sulfur dioxide gas are harmful to the human body, when using them, it is necessary to prevent the gas from leaking into the workplace and to neutralize it before releasing it, which places a burden on equipment. big. The present invention uses a harmless gas such as air at a high temperature instead of a harmful gas.In addition to not requiring special equipment, a wooden mold can be used, and the mold material mixture has a sufficient pot life. , mold productivity is also good. The present invention will be explained in detail below. The binder used in the present invention is an acid-curing resin such as a furan resin or a phenolic resin, and the acid-curing resins currently used in self-hardening molds can be used as they are. The curing catalyst is a salt consisting of a strong acid and a weak base.
For example, when ammonium hydrogen sulfate or ammonium persulfate is used, it easily decomposes in hot gas, releases ammonium, which is a weak base, and leaves behind a strong acid.
Rapidly cures acid-curing resins. Furthermore, these salts do not easily decompose even when mixed with acid-curing resins, and have a sufficient pot life as a molding material mixture. Various methods have been tried in the past to harden the resin in the mold material mixture with high-temperature gas, but conventional methods involve applying a low concentration of acid to acid-curing resins, or applying weak acids to shorten the pot life. This method is either a method of curing by increasing the temperature and accelerating the reaction by increasing the temperature, or using a resin containing an organic solvent that is relatively easy to scatter, and curing by scattering the solvent. The curing properties were not sufficient. The present invention is based on a new method in which a salt consisting of a strong acid and a weak base substance is used as a catalyst, and after molding a mold material mixture, the mixture is converted into a strong acid by blowing high-temperature gas and hardened rapidly. The pot life of the mold material mixture is sufficiently long, and the curing properties with high-temperature gas far exceed those of conventional methods. In addition, with large molds, the penetration of high temperature gas may be insufficient, or the temperature may drop while passing through the mold, resulting in poor hardening in some areas. Vent holes are provided in the mold material to suck the air between the sand particles of the mold material, or a vibrator is attached to the model surface plate to apply slight vibrations, creating a fine gap between the model and the mold material mixture while creating a high temperature. Curing properties can be improved by blowing gas. The present invention will be specifically explained below using Examples. [Example 1] 100 g of ammonium hydrogen sulfate and 100 g of water were placed in a container and stirred to prepare a curing catalyst with a concentration of 50%. Next, add 50g of curing catalyst to 10kg of silica sand and make approximately
After mixing for 30 seconds, 100 g of furan resin was added and mixed for 1 minute to obtain a mold material mixture. Here, the mold material mixture is filled into a split mold having three cavities each having a diameter of 50 mm and a height of 50 mm at regular intervals, and air between the mold material mixture is sucked through a vent hole provided at the bottom of the mold. High-temperature air was sucked into the upper part using a hot air blower for about 2 minutes. The strength of the mold obtained here immediately after ventilation and the strength the next day are shown in relation to the elapsed time after preparing the mold material mixture as follows.

〔実施例 2〕[Example 2]

実施例1と同じように鋳型材混合物を作成した
のち、あらかじめ準備した振動テーブル上に模型
定盤と鋳枠を乗せ、その鋳枠中へ約8Kgの鋳型材
混合物を投入し、軽くつき固めた後、微振動を与
えつつ、模型面にとりつけたベントホールを通し
て鋳型材粒子間の空気を吸引し、鋳型背面をバー
ナで約2分間あぶつた。その後ただちに抜型し、
硬度計で模型に接した鋳型表面の硬度を測定し
た。その結果は硬度97以上で、鋳型内部も十分に
硬化していた。この結果より本鋳物砂混合物は十
分な硬化性をそなえていることが認められた。
After creating a mold material mixture in the same manner as in Example 1, the model surface plate and casting flask were placed on a vibrating table prepared in advance, and approximately 8 kg of the mold material mixture was poured into the flask and lightly tamped. Thereafter, while applying slight vibrations, the air between the particles of the mold material was sucked through a vent hole attached to the model surface, and the back surface of the mold was heated with a burner for about 2 minutes. Then immediately cut out the mold,
The hardness of the mold surface in contact with the model was measured using a hardness meter. The hardness was over 97, and the inside of the mold was also sufficiently hardened. From this result, it was confirmed that this foundry sand mixture had sufficient hardenability.

Claims (1)

【特許請求の範囲】 1 鋳物砂にフラン樹脂、フエノール樹脂等の酸
硬化性樹脂と、強酸と弱塩基物質からなる塩を加
えて鋳型材混合物を作り、鋳型を造型したのち、
高温ガスを通気して、急速に硬化させることを特
徴とする鋳型の製造法。 2 上記鋳型材混合物で鋳型を造型したのち、模
型面にとりつけたベントホールを通して、鋳型材
粒子間の空気を吸引し、鋳型背面より供給する高
温のガスの通気をよくして硬化させる特許請求の
範囲第1項記載の鋳型の製造法。 3 上記鋳型材混合物で鋳型を造型したのち、模
型定盤を微振動させ、高温のガスを通気して硬化
させる特許請求の範囲第1項記載の鋳型の製造
法。
[Claims] 1. A molding material mixture is prepared by adding an acid-curing resin such as a furan resin or a phenolic resin and a salt consisting of a strong acid and a weak basic substance to foundry sand, and after forming a mold,
A mold manufacturing method characterized by rapid hardening by aeration of high-temperature gas. 2. After forming a mold using the above mold material mixture, the air between the mold material particles is sucked through a vent hole attached to the model surface, and the hot gas supplied from the back of the mold is cured by improving ventilation. A method for manufacturing a mold according to scope 1. 3. The method of manufacturing a mold according to claim 1, wherein after molding a mold with the mold material mixture, a model surface plate is slightly vibrated and a high temperature gas is passed through to harden the mold.
JP10734884A 1984-05-25 1984-05-25 Production of casting mold by high-temperature gas Granted JPS60250853A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10734884A JPS60250853A (en) 1984-05-25 1984-05-25 Production of casting mold by high-temperature gas

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10734884A JPS60250853A (en) 1984-05-25 1984-05-25 Production of casting mold by high-temperature gas

Publications (2)

Publication Number Publication Date
JPS60250853A JPS60250853A (en) 1985-12-11
JPS6124099B2 true JPS6124099B2 (en) 1986-06-09

Family

ID=14456774

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10734884A Granted JPS60250853A (en) 1984-05-25 1984-05-25 Production of casting mold by high-temperature gas

Country Status (1)

Country Link
JP (1) JPS60250853A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20230081794A (en) * 2021-11-29 2023-06-08 한국생산기술연구원 Cellulose nanofiber based carbon nanomaterial nanowire exothermic coating flexible heating film and manufacturing method thereof

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5986457B2 (en) 2011-08-31 2016-09-06 花王株式会社 Self-hardening binder composition for mold making
CN104985109A (en) * 2015-07-06 2015-10-21 安徽三联泵业股份有限公司 Modified casting sand used for casting pump body and adopting furan resin loaded with carbon nanometer fibers

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54112329A (en) * 1978-02-22 1979-09-03 Mitsubishi Heavy Ind Ltd Hardening promotion of furan sand casting mold
US4317763A (en) * 1980-03-24 1982-03-02 The Quaker Oats Company Catalysts and binder systems for manufacturing sand shapes

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20230081794A (en) * 2021-11-29 2023-06-08 한국생산기술연구원 Cellulose nanofiber based carbon nanomaterial nanowire exothermic coating flexible heating film and manufacturing method thereof

Also Published As

Publication number Publication date
JPS60250853A (en) 1985-12-11

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