JPH0557393A - Moldrelease agent for green sand used for casting - Google Patents

Moldrelease agent for green sand used for casting

Info

Publication number
JPH0557393A
JPH0557393A JP21562991A JP21562991A JPH0557393A JP H0557393 A JPH0557393 A JP H0557393A JP 21562991 A JP21562991 A JP 21562991A JP 21562991 A JP21562991 A JP 21562991A JP H0557393 A JPH0557393 A JP H0557393A
Authority
JP
Japan
Prior art keywords
acid
sand
mold
casting
water
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.)
Granted
Application number
JP21562991A
Other languages
Japanese (ja)
Other versions
JP3094115B2 (en
Inventor
Shugyo Uehara
主行 上原
Kiyoshi Shinkai
潔 新開
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.)
Individual
Original Assignee
Individual
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Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to JP03215629A priority Critical patent/JP3094115B2/en
Publication of JPH0557393A publication Critical patent/JPH0557393A/en
Application granted granted Critical
Publication of JP3094115B2 publication Critical patent/JP3094115B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To provide moldrelease agent for green sand used for casting, which has excellent mold releasing property and stability, etc., and can be efficiently cast. CONSTITUTION:The moldrelease agent for green sand used to casting, is colloid solution prepared by stirring and mixing mixed liquid containing surfactant, fatty acid, amine and water into basic oil composed or mineral oil and/or petroleum solvent.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、鋳造する際に使用する
生砂型の成型に用いる離型剤に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a release agent used for molding a green sand mold used for casting.

【0002】[0002]

【従来技術とその問題点】一般に鋳造における鋳型には
砂型が最も多く用いられており、その砂型の造型作業に
際しては模型と生砂との脱型性を良くし、模型の摩耗を
少なくする必要がある。つまり、上記模型には金型、木
型、樹脂型等の種類があり、金型材料としては鋳鉄、ア
ルミニウム、合金等、木型材料としては杉、檜等、樹脂
型材料としてはエポキシ樹脂等がそれぞれ用いられてい
る。これらの模型は造型される際に生砂と擦れ合うた
め、摩耗が大きく且つ連続使用する場合には初期設計寸
法が変化し、精度ある製品を得ることが困難となる。ま
た、模型と生砂との密着により「型おち」や「脱型不
良」が生じる。そこで模型と生砂との密着を防ぎ、滑り
を良くするために離型剤が利用されている。
2. Description of the Related Art Generally, a sand mold is most often used as a mold in casting, and it is necessary to improve the demolding property between the model and the fresh sand and reduce the wear of the model during the molding work of the sand mold. There is. That is, there are types of molds, wood molds, resin molds, etc. in the model, the mold material is cast iron, aluminum, alloy, etc., the wood mold material is cedar, cypress, etc., and the resin mold material is epoxy resin, etc. Are used respectively. Since these models rub against raw sand when they are molded, they are greatly worn and the initial design dimensions change when continuously used, making it difficult to obtain accurate products. In addition, the close contact between the model and the green sand causes “mold bottom” and “demolding failure”. Therefore, a release agent is used to prevent the model from sticking to the green sand and to improve the slip.

【0003】このような鋳物生砂型用の離型剤に要求さ
れる基本的な性能は、1)模型と生砂との密着を防ぐため
に適度で均一な膜を成形すること。2)模型上へ生砂が均
一に流れるように生砂の滑りを良くすること。3)成型さ
れた砂型に鋳物の溶湯を流し込んだ際に多量のガスを発
生したり、砂型の通気性及び強度に悪影響を与えないこ
と。4)模型が腐食したり、溶解しないこと。5)安価であ
ること。等が挙げられる。
The basic performance required for such a mold release agent for a green mold for casting is 1) forming a proper and uniform film to prevent the model and the green sand from sticking to each other. 2) To improve the smoothness of the raw sand so that it flows evenly onto the model. 3) Do not generate a large amount of gas when pouring the molten metal of the casting into the molded sand mold, and do not adversely affect the air permeability and strength of the sand mold. 4) The model should not corrode or dissolve. 5) Be inexpensive. Etc.

【0004】従来からの離型剤としては、通常は石油系
溶剤に脂肪酸、ワックス、エステル、油脂、界面活性剤
等を溶解させた油性系離型剤が使用されている。しかし
ながら、上記石油系溶剤は主として灯油が使用されてい
るが、灯油は一般に粘度が1〜3cSt程度(40℃)
と低いため、模型に噴霧した際に薄い油膜か形成され
ず、生砂を入れて圧縮した場合には更に油膜が薄くなる
傾向があり、模型と生砂が密着し易くなる。このため、
一回の離型剤の塗布で造型できる回数(連続造型回数)
は少なくなる。また樹脂型や模型の摩耗防止のために硬
質クロムメッキされた型のように、その表面が緻密であ
る場合或いは砂の温度上昇に伴い塗膜粘度が低下した場
合等には離型性能は低下するおそれがある。さらに灯油
は引火点が通常 50℃程度と低いので、引火の危険性
を伴い、消防法の規制も受け、使用に際して細心の注意
が必要となる。一方、これら欠点を改善する方法として
粘度及び引火点の高い石油系鉱油の使用も考えられる
が、これらは一般に油膜の粘着性が高いために「型落
ち」が生じる。
As a conventional release agent, an oil-based release agent prepared by dissolving a fatty acid, a wax, an ester, a fat and an oil, a surfactant and the like in a petroleum solvent is usually used. However, although kerosene is mainly used as the petroleum solvent, the viscosity of kerosene is generally about 1 to 3 cSt (40 ° C).
Therefore, when sprayed on the model, a thin oil film is not formed, and when the fresh sand is put and compressed, the oil film tends to be further thinned, and the model and the raw sand tend to adhere to each other. For this reason,
Number of times molding can be performed with a single release agent application (continuous molding times)
Will be less. In addition, the mold release performance decreases when the surface is dense, such as a resin mold or a mold plated with hard chrome to prevent abrasion of the model, or when the viscosity of the coating film decreases as the sand temperature rises. May occur. Furthermore, since kerosene has a low flash point, which is usually around 50 ° C, there is a risk of ignition, and it is subject to the regulations of the Fire Service Law, so it is necessary to exercise extreme caution when using it. On the other hand, use of petroleum-based mineral oil having a high viscosity and a high flash point can be considered as a method for improving these drawbacks, but these generally cause "mold loss" due to the high tackiness of the oil film.

【0005】上記離型剤のもつ問題を解決するために油
中水形エマルション離型剤(特公昭63−29625
号)が提案され、利用されている。これは前記油性離型
剤のうち引火点が55℃以上の油溶性離型剤を主成分と
し、必要に応じ界面活性剤を用いて水を10〜60%加
え、攪拌混合することにより油中水形エマルションとし
た離型剤である。
In order to solve the problem of the above-mentioned mold release agent, a water-in-oil emulsion mold release agent (Japanese Patent Publication No. 63-29625).
No.) has been proposed and used. This is because the main component is the oil-soluble mold release agent having a flash point of 55 ° C. or higher among the above oily mold release agents, and if necessary, 10 to 60% of water is added using a surfactant, and the mixture is stirred and mixed in the oil. It is a release agent in the form of a water-based emulsion.

【0006】しかしながら、上記離型剤では次に示すよ
うな問題点がある。
However, the above releasing agent has the following problems.

【0007】1)エマルション化されているため、温度
変動によってエマルション粒子の安定性が低下し、長期
保存の場合には分離してしまうおそれがある。
1) Since the emulsion is emulsified, the stability of the emulsion particles is lowered due to temperature fluctuation, and there is a risk of separation during long-term storage.

【0008】2)使用する石油系溶剤と水の密度差があ
るため、製造時にエマルションの均一化を図る必要があ
り、プロペラ攪拌のような簡単な方法では充分な攪拌が
行なえず、ホモヂナイザー等の装置が必要となる。尚プ
ロペラ攪拌による場合には3時間以上の攪拌を行なわな
いと均一なエマルションが得られない。エマルション粒
子の大きさが均一でない場合には上層と下層で粒子径分
布が異なる傾向になり、均一な性能が得難くなる。
2) Since there is a difference in the density of the petroleum solvent used and water, it is necessary to make the emulsion uniform during production, and sufficient stirring cannot be performed by a simple method such as propeller stirring. Equipment is required. In the case of stirring with a propeller, a uniform emulsion cannot be obtained unless stirring is performed for 3 hours or more. If the size of the emulsion particles is not uniform, the particle size distribution tends to differ between the upper layer and the lower layer, and it becomes difficult to obtain uniform performance.

【0009】3)水が10〜60%と多量であるため、
鋳鉄の模型の場合には残留水分の影響により錆が発生す
る。
3) Since the amount of water is as large as 10 to 60%,
In the case of cast iron model, rust occurs due to the effect of residual moisture.

【0010】4)造型用砂型に用いる生砂は主に砂(山
砂、川砂、浜砂、けい砂等)、結合剤(粘土、ベントナ
イト等)、及び添加剤(石炭粉、ピッチ粉、コークス
粉、黒鉛粉末等)からなっている。この中の結合剤につ
いては、粘結力を上げるために水を添加しているが、水
の添加量が多い場合には砂型の必要条件である通気性や
強度が低下する傾向にあり、それ故に含有水分量は2〜
8%程度が適切とされている。しかし、この油中水形エ
マルションタイプの水分量では模型と生砂との境界面で
過水分となり易く、粘結剤の結合力が低下し、鋳物成型
不良にまでは至らなくとも模型表面に生砂が残る傾向が
ある。また、これを解決するためには塗布量をできるだ
け少なくする必要が生じ、噴霧量を調節するのに手間が
かかり、さらに粘結剤に水分が吸収されない工夫も要求
される。
4) The raw sand used in the molding sand mold is mainly sand (mountain sand, river sand, beach sand, silica sand, etc.), binders (clay, bentonite, etc.), and additives (coal powder, pitch powder, coke powder). , Graphite powder, etc.). Regarding the binder in this, water is added to increase the cohesive strength, but when the amount of water added is large, the air permeability and strength, which are the necessary conditions for the sand mold, tend to decrease. Therefore, the water content is 2
About 8% is considered appropriate. However, with this water-in-oil emulsion type water content, excess water is likely to occur at the interface between the model and the green sand, the binding force of the binder decreases, and even if casting molding defects do not occur, the water will form on the model surface. There is a tendency for sand to remain. Further, in order to solve this, it is necessary to reduce the amount of application as much as possible, it takes time and effort to adjust the amount of spraying, and a device is required to prevent the binder from absorbing water.

【0011】従って、現在では上記の問題を解消できる
新規な離型剤の開発が切望されている。
Therefore, at present, there is a strong demand for the development of a new release agent that can solve the above problems.

【0012】[0012]

【問題点を解決するための手段】本発明は、優れた脱型
性、安定性等を有し、効率良く鋳造することができる鋳
物生砂用離型剤を提供することを目的とする。
DISCLOSURE OF THE INVENTION It is an object of the present invention to provide a mold releasing agent for molding raw sand which has excellent demolding property, stability and the like and can be efficiently cast.

【0013】本発明者らは、上記問題を解決すべく鋭意
研究を重ねた結果、特定組成を有するコロイド溶液によ
り上記目的を達成できることを見出し、本発明を完成す
るに至った。
As a result of intensive studies to solve the above problems, the present inventors have found that the above object can be achieved by a colloidal solution having a specific composition, and have completed the present invention.

【0014】即ち、本発明は、鉱油及び/又は石油系溶
剤からなる基油に界面活性剤、脂肪酸、アミン及び水を
含有させた混合液を攪拌・混合してなるコロイド溶液で
あることを特徴とする鋳物生砂用離型剤に係るものであ
る。
That is, the present invention is a colloidal solution obtained by stirring and mixing a mixed solution of a base oil comprising a mineral oil and / or a petroleum solvent with a surfactant, a fatty acid, an amine and water. The present invention relates to a mold release agent for green sand.

【0015】以下、本発明について詳細に説明する。The present invention will be described in detail below.

【0016】本発明の基油は、鉱油又は石油系溶剤の単
独のもの、或いは両者を併用したものを用いる。上記鉱
油としては公知のものが使用でき、例えばマシン油、ニ
ュートラルオイル(高級潤滑油基油)等の各種鉱油が例
示でき、また上記石油系溶剤についても灯油、軽油等の
公知の各種石油軽質油が例示できる。尚、基油は噴霧性
及び脱型性の見地よりその動粘度が10cSt以下であ
るものが好ましい。
As the base oil of the present invention, a mineral oil or a petroleum solvent is used alone, or both are used in combination. As the mineral oil, known mineral oils can be used, for example, various mineral oils such as machine oil and neutral oil (high-grade lubricating base oil) can be exemplified, and the petroleum-based solvent can also be known various petroleum light oils such as kerosene and light oil. Can be illustrated. The base oil preferably has a kinematic viscosity of 10 cSt or less from the viewpoint of sprayability and demoldability.

【0017】界面活性剤としてはノニオン系界面活性
剤、アニオン系界面活性剤、カチオン系界面活性剤、両
性界面活性剤等の公知のものが使用できるが、特にノニ
オン系界面活性剤、アニオン系界面活性剤が良く、ノニ
オン系界面活性剤としては例えば高級アルコールアルキ
レンオキサイド付加物、ノニルフェノールアルキルオキ
サイド付加物、脂肪酸アルキレンオキサイド付加物、グ
リセリン脂肪酸エステル、ポリアルキレングリコール脂
肪酸エステル、ソルビタン脂肪酸エステル、ソルビタン
脂肪酸エステルのアルキレンオキサイド付加物、脂肪酸
アマイド、脂肪酸アマイドのアルキレンオキサイド付加
物、ポリエチレン−ポリオキシプロピレン縮合物等が挙
げられる。またアニオン系界面活性剤としては例えば高
級脂肪酸、ナフテン酸、アルキルスルホン酸、アルキル
ナフタリンスルホン酸、石油スルホン酸、アルキルベン
ゼンフォスフォン酸のアルカリ塩、アルキルベンゼンフ
ォスフォン酸のアミン塩、アルキルベンゼンフォスフォ
ン酸のアンモニア塩、アルキルベンゼンフォスフォン酸
のアルキル硫酸エステル、硫酸化油、硫酸化脂肪族モノ
グリセライド、硫酸化アルカノールアミド、硫酸化エー
テル、アルキルリン酸エステル等が挙げられる。これら
界面活性剤の添加量は2〜10重量%とするのが好まし
い。2重量%を下回るとコロイド溶液が充分に得られ
ず、10重量%を上回ると粘度が上昇し、粘着性が発現
されるために充分な脱型性が得られない。
As the surfactant, known ones such as nonionic surfactants, anionic surfactants, cationic surfactants and amphoteric surfactants can be used, but especially nonionic surfactants and anionic surfactants. Activators are good, and examples of nonionic surfactants include higher alcohol alkylene oxide adducts, nonylphenol alkyl oxide adducts, fatty acid alkylene oxide adducts, glycerin fatty acid esters, polyalkylene glycol fatty acid esters, sorbitan fatty acid esters, and sorbitan fatty acid esters. Examples thereof include alkylene oxide adducts, fatty acid amides, alkylene oxide adducts of fatty acid amides, and polyethylene-polyoxypropylene condensates. Examples of the anionic surfactant include higher fatty acid, naphthenic acid, alkylsulfonic acid, alkylnaphthalenesulfonic acid, petroleum sulfonic acid, alkali salt of alkylbenzenephosphonic acid, amine salt of alkylbenzenephosphonic acid, and ammonia of alkylbenzenephosphonic acid. Examples thereof include salts, alkyl sulfates of alkylbenzenephosphonic acid, sulfated oils, sulfated aliphatic monoglycerides, sulfated alkanolamides, sulfated ethers and alkyl phosphates. The addition amount of these surfactants is preferably 2 to 10% by weight. If it is less than 2% by weight, a colloidal solution cannot be obtained sufficiently, and if it exceeds 10% by weight, the viscosity increases and the tackiness is exhibited, so that sufficient demolding property cannot be obtained.

【0018】脂肪酸としては、炭素数8以上の高級脂肪
酸が好ましく、例えばカプリル酸、ペラルゴン酸、カプ
リン酸、ウンデシル酸、ラウリン酸、ミリスチン酸、パ
ルミチン酸、ステアリン酸、アラキッド酸、ベーエン酸
等の直鎖飽和脂肪酸、カプロレイン酸、ウンデシレン
酸、ラウロレイン酸、ミリストレイン酸、パルミトレイ
ン酸、オレイン酸、エライジン酸等の直鎖不飽和脂肪
酸、イソオクタン酸、イソノナン酸、イソステアリン酸
等の分枝脂肪酸、ワックス等を酸化して得られる有機
酸、アビエチン酸等の樹脂酸、カプリン二酸等のダイマ
ー酸及びトリマー酸等の各種公知の脂肪酸が挙げられ
る。その添加量は0.5〜2重量%とするのが好まし
い。0.5重量%未満では添加効果がなく、「型落ち」
が発生し、充分な脱型性が得られず、一方2重量%を超
える場合は粘着性が過度に高くなり、この場合にも充分
な脱型性が得られなくなる。本発明における脂肪酸は、
脱型性を向上させる役割を果たす。
As the fatty acid, a higher fatty acid having 8 or more carbon atoms is preferable, and for example, a direct fatty acid such as caprylic acid, pelargonic acid, capric acid, undecyl acid, lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid, behenic acid, etc. Chain unsaturated fatty acids, caproleic acid, undecylenic acid, lauroic acid, myristoleic acid, palmitoleic acid, oleic acid, linear unsaturated fatty acids such as elaidic acid, branched fatty acids such as isooctanoic acid, isononanoic acid, isostearic acid, wax, etc. Examples thereof include organic acids obtained by oxidation, resin acids such as abietic acid, dimer acids such as capric diacid, and various known fatty acids such as trimer acid. The added amount is preferably 0.5 to 2% by weight. If it is less than 0.5% by weight, there is no addition effect and "mold loss"
Occurs, and sufficient releasability cannot be obtained. On the other hand, when it exceeds 2% by weight, tackiness becomes excessively high, and in this case also sufficient releasability cannot be obtained. The fatty acid in the present invention is
It plays a role of improving demolding property.

【0019】アミンとしては、公知の各種アミン類を用
いることができ、例えばモノエタノールアミン、ジエタ
ノールアミン、トリエタノールアミン、モノイソプロパ
ノールアミン、ミックスイソプロパノールアミン、n−
プロパノールアミン、トリイソプロパノールアミン等の
アルカノールアミン類、モルホリン、n−アミノプロピ
ルモルホリン、n−アルキルモルホリン等のモルホリン
系アミン化合物類、ピロリジン、n−メチル−2ヒドロ
キシエチルピロリジン、2−ヒドロキシメチルピロリジ
ン等のピロリジン系アミン化合物類、ピペラジン、1−
アミノ−4メチルピペラジン等のピペラジン系アミン化
合物類、ヘキサヒドロ1,3,5トリ(2−ヒドロキシ
エチル)S−トリアジン、ヘキサヒドロ1,3,5トリ
エチルS−トリアジン、6−フェニル−2,4−ジアミ
ノ−トリアジン等のトリアジン系アミン化合物類、シク
ロヘキシルアミン、ジシクロヘキシルアミン等の環状ア
ミン類、ジイソプロピルアミン、n−ブチルアミン、イ
ソブチルアミン、イソアミルアミン、メチルヘキシルア
ミン等の脂肪族アミン類等が挙げられる。その添加量は
混合液100重量部に対して0.02〜1重量部とする
のが好ましい。0.02重量部未満では充分なコロイド
溶液が得られず、1重量部を上回ると脂肪酸との反応に
より粘着性が増大し、充分な脱型性が発揮されないので
好ましくない。アミンの添加により安定性に優れたコロ
イド溶液が得られる。尚、本発明でいうコロイド溶液と
はボシュロム式分光光度計による透過率測定において波
長524nmで蒸留水を100%とした場合に10%以上
の透過率を示すものを意味する。
As the amine, various known amines can be used, for example, monoethanolamine, diethanolamine, triethanolamine, monoisopropanolamine, mixed isopropanolamine, n-.
Alkanolamines such as propanolamine and triisopropanolamine, morpholine-based amine compounds such as morpholine, n-aminopropylmorpholine and n-alkylmorpholine, pyrrolidine, n-methyl-2hydroxyethylpyrrolidine, 2-hydroxymethylpyrrolidine and the like. Pyrrolidine-based amine compounds, piperazine, 1-
Amino-4methylpiperazine and other piperazine amine compounds, hexahydro 1,3,5 tri (2-hydroxyethyl) S-triazine, hexahydro 1,3,5 triethyl S-triazine, 6-phenyl-2,4-diamino Examples include triazine-based amine compounds such as triazine, cyclic amines such as cyclohexylamine and dicyclohexylamine, and aliphatic amines such as diisopropylamine, n-butylamine, isobutylamine, isoamylamine, and methylhexylamine. The addition amount thereof is preferably 0.02 to 1 part by weight with respect to 100 parts by weight of the mixed solution. If it is less than 0.02 part by weight, a sufficient colloidal solution cannot be obtained, and if it exceeds 1 part by weight, the reaction with fatty acid increases the tackiness and sufficient demolding property is not exhibited, which is not preferable. Addition of amine gives a colloidal solution with excellent stability. The colloidal solution referred to in the present invention means a solution showing a transmittance of 10% or more when the distilled water is taken as 100% at a wavelength of 524 nm in the transmittance measurement by a Bausch & Lomb type spectrophotometer.

【0020】水は、3〜10重量%加えるのが望まし
い。3重量%を下回ると塗膜強度が低下し、脱型性能が
油性離脱剤と同程度となり、充分な効果が得られない。
10重量%を上回ると生砂の含有水分量より多くなり過
ぎるため、粘土の粘結力に影響を与え、模型に生砂が残
留する原因となる。さらに混合液がコロイド溶液になり
にくく、エマルション状態となり好ましくない。
Water is preferably added in an amount of 3 to 10% by weight. If the amount is less than 3% by weight, the strength of the coating film is lowered, and the demolding performance is almost the same as that of the oil-based releasing agent, and a sufficient effect cannot be obtained.
If it exceeds 10% by weight, the content of water in the raw sand will be too much, which will affect the caking force of the clay and cause the raw sand to remain in the model. Furthermore, it is not preferable that the mixed liquid becomes a colloidal solution and becomes an emulsion state.

【0021】また、上記の各成分の他に必要に応じて香
料等の各種添加剤を加えても良い。本発明離型剤の調製
方法は、その一例としてまず基油に脂肪酸及び界面活性
剤を所定量加えてプロペラ攪拌にて均一になるように混
合し、次いでこれに所定量の水を加えて均一に混合でき
たところで所定量のアミンを添加すれば本発明離型剤が
得られる。この場合、混合温度は常温で溶解するものに
ついては常温で調製できるが、例えば常温で固形の添加
剤で加温を必要とするものについては任意の温度で加温
して調製する。また攪拌時間は、各成分を配合した後、
通常約10分〜1時間行なえば本発明のコロイド溶液が
得られる。攪拌方法はホモヂナイザーにより行なうのが
好ましいが、従来の油中水形エマルションを製造する場
合と異なりプロペラ攪拌のような簡単な方法でも同様の
効果が得られる。
In addition to the above components, various additives such as fragrances may be added if necessary. As an example of the method for preparing the release agent of the present invention, first, a predetermined amount of a fatty acid and a surfactant are added to a base oil and mixed so as to be homogeneous by propeller stirring, and then a predetermined amount of water is added to the mixture to make a uniform mixture. When a predetermined amount of amine is added when it has been mixed, the release agent of the present invention can be obtained. In this case, the mixing temperature can be prepared at room temperature if it dissolves at room temperature, but, for example, if the additive is solid at room temperature and requires heating, it is prepared at any temperature. In addition, the stirring time is
Usually, the colloidal solution of the present invention can be obtained after about 10 minutes to 1 hour. The stirring method is preferably performed with a homogenizer, but unlike the conventional case of producing a water-in-oil emulsion, the same effect can be obtained by a simple method such as propeller stirring.

【0022】本発明離型剤の使用に際しては、例えば、
通常のハンドスプレー又は自動噴霧装置を用い、生砂型
の成型に用いる模型に噴霧すれば良い。
In using the release agent of the present invention, for example,
A normal hand sprayer or an automatic spraying device may be used to spray the model used for molding the green sand mold.

【0023】[0023]

【発明の効果】本発明の鋳物生砂用離型剤は、従来の油
中水形エマルション離型剤に比して、優れた脱型性を達
成できるのはもとより、それ自体簡単なプロペラ攪拌で
調製することができ、また微細な粒子からなるために製
品の品質が一定であり安定性、噴霧性等に優れている。
さらに水分含有量が少ないために錆の発生が有効に抑制
できる。
INDUSTRIAL APPLICABILITY The mold releasing agent of the present invention for casting raw sand can achieve excellent demolding property as compared with the conventional water-in-oil type emulsion mold releasing agent, and it itself has a simple propeller stirring. The product quality is constant because it is composed of fine particles, and stability and sprayability are excellent.
Furthermore, since the water content is low, the generation of rust can be effectively suppressed.

【0024】一方、従来の油性系離型剤に比して、一定
の水分を含有しているので引火が起こりにくく、しかも
基油の引火点が80℃以上の場合には引火点が実質的に
認められず、安全面においても優れた効果を発揮する。
On the other hand, since it contains a certain amount of water as compared with the conventional oil-based mold release agent, it is less likely to catch fire, and when the base oil has a flash point of 80 ° C. or higher, the flash point is substantially It is not recognized in the above, and exerts an excellent effect in terms of safety.

【0025】[0025]

【実施例】以下に実施例を示し、本発明の特徴とすると
ころをより一層明瞭にする。但し、本発明は実施例のみ
に限定されない。
EXAMPLES Examples will be shown below to further clarify the characteristics of the present invention. However, the present invention is not limited to the examples.

【0026】尚、実施例及び比較例中の%はすべて重量
%を示す。
All percentages in the examples and comparative examples are% by weight.

【0027】実施例1〜10 第1表に示すような各成分を用い、混合・攪拌すること
によりコロイド溶液とし、本発明離型剤を調製した。
Examples 1 to 10 The components shown in Table 1 were used and mixed and stirred to prepare a colloidal solution, to prepare the release agent of the present invention.

【0028】得られた本発明離型剤の安定性、摩擦係
数、透過率、防錆性及び離型性能について物性試験を行
なった。その結果も第1表に示す。尚、物性試験及びは
下記の測定方法により行なった。
The physical properties of the obtained releasing agent of the present invention were tested for stability, friction coefficient, transmittance, rustproofing property and releasing performance. The results are also shown in Table 1. The physical property test and the measurement were carried out by the following measuring methods.

【0029】a)安定性試験…200mlビーカーに試料
として離型剤200mlを入れ、室温下で24時間放置し
た後、上層部と下層部をスポイトで採取し、粘度を測定
し、下層粘度/上層粘度の値により評価した。
A) Stability test: 200 ml of a mold release agent was put into a 200 ml beaker as a sample and left at room temperature for 24 hours. Then, the upper layer part and the lower layer part were sampled with a dropper, and the viscosity was measured. Lower layer viscosity / upper layer It was evaluated by the value of viscosity.

【0030】b)摩擦係数…室温下で振子式油性試験機
I型を用いて測定した。
B) Friction coefficient: Measured at room temperature using a pendulum type oiliness tester type I.

【0031】c)透過率…ボシュロム式分光光度計を用
い、波長524nmにおける透過率を蒸留水で100%と
し、試料の透過率を測定した。また外観についても観察
した。 d)防錆試験…テストピース(FC−20、20mm×7
0mm×5mm)を試料に一旦全部浸漬した後、試料50ml
を入れた100mlのビーカーにテストピースを半浸漬の
状態に入れ、湿度90%温度50℃に保持した恒温恒湿
槽内に1時間静置し、その気相部及び液相部における錆
の発生状態を確認した。評価基準は以下の通りである。
C) Transmittance: Using a Bausch & Lomb type spectrophotometer, the transmittance at a wavelength of 524 nm was adjusted to 100% with distilled water, and the transmittance of the sample was measured. The appearance was also observed. d) Anticorrosion test: Test piece (FC-20, 20mm × 7
(0 mm x 5 mm) is completely immersed in the sample and then 50 ml of the sample
Put the test piece in a 100 ml beaker containing the water in a semi-immersed state, and leave it in a constant temperature and humidity chamber at a humidity of 90% and a temperature of 50 ° C for 1 hour to generate rust in the gas phase and the liquid phase. I confirmed the condition. The evaluation criteria are as follows.

【0032】 (気相部)A…10%以下の薄い錆が発生 B…30%以下の薄い錆が発生 C…30%未満の濃い錆が発生 D…30%以上の濃い錆が発生 (液相部)A…変色及び錆の発生なし B…灰色の変色 C…黒色の変色 D…赤褐色の変色(錆発生) e)離型性能試験…下記I〜III の試験を行なった。模
型への生砂の残留や型落ち等の造型不良が認められない
場合を造型可能とし、表中にはその連続造型回数を示
す。
(Vapor portion) A ... 10% or less thin rust occurs B ... 30% or less thin rust C ... less than 30% thick rust D ... 30% or more thick rust occurs (liquid Phase part) A ... No discoloration and rust generation B ... Gray discoloration C ... Black discoloration D ... Reddish brown discoloration (rust generation) e) Releasing performance test: The following tests I to III were performed. Molding is allowed when no molding defect such as residual sand on the model or mold drop is observed, and the number of continuous molding is shown in the table.

【0033】(試験I)ジョルトスクイズ造型機を用
い、継手の鋳鉄製模型に1秒間スプレー塗布した後、連
続して造型を行なった。
(Test I) Using a Jolt squeeze molding machine, a cast iron model of a joint was spray-coated for 1 second and then continuously molded.

【0034】(試験II)試験Iの方法で3秒間スプレー
塗布した後、連続して造型を行なった。
(Test II) After spray coating for 3 seconds by the method of Test I, continuous molding was performed.

【0035】(試験 III)ジョルトスクイズ造型機を用
い、切削機具の樹脂製模型に1秒間スプレー塗布した
後、連続して造型を行なった。
(Test III) A Jolt squeeze molding machine was used to spray-apply a resin model of a cutting machine tool for 1 second, followed by continuous molding.

【0036】[0036]

【表1】 [Table 1]

【0037】[0037]

【表2】 [Table 2]

【0038】比較例1〜2 第2表に示すような成分を用いて実施例と同様にして離
型剤を調製し、その物性試験を行なった。その結果も第
2表に示す。
Comparative Examples 1-2 A mold release agent was prepared in the same manner as in Examples using the components shown in Table 2, and its physical properties were tested. The results are also shown in Table 2.

【0039】比較例3 市販の油性系鋳物生砂用離型剤を用いて実施例と同様に
物性試験を行なった。その結果を第2表に示す。
Comparative Example 3 A physical property test was conducted in the same manner as in the examples using a commercially available mold release agent for oil-based foundry sand. The results are shown in Table 2.

【0040】[0040]

【表3】 [Table 3]

【0041】以上の結果より、本発明の離型剤は従来の
ものに比して極めて優れた性能を発揮していることがわ
かる。
From the above results, it can be seen that the releasing agent of the present invention exhibits extremely excellent performance as compared with the conventional one.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】鉱油及び/又は石油系溶剤からなる基油に
界面活性剤、脂肪酸、アミン及び水を含有させた混合液
を攪拌・混合してなるコロイド溶液であることを特徴と
する鋳物生砂用離型剤。
1. A casting raw material, which is a colloidal solution obtained by stirring and mixing a mixed solution of a base oil comprising a mineral oil and / or a petroleum solvent with a surfactant, a fatty acid, an amine and water. Release agent for sand.
JP03215629A 1991-08-27 1991-08-27 Mold release agent for green sand Expired - Fee Related JP3094115B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP03215629A JP3094115B2 (en) 1991-08-27 1991-08-27 Mold release agent for green sand

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP03215629A JP3094115B2 (en) 1991-08-27 1991-08-27 Mold release agent for green sand

Publications (2)

Publication Number Publication Date
JPH0557393A true JPH0557393A (en) 1993-03-09
JP3094115B2 JP3094115B2 (en) 2000-10-03

Family

ID=16675572

Family Applications (1)

Application Number Title Priority Date Filing Date
JP03215629A Expired - Fee Related JP3094115B2 (en) 1991-08-27 1991-08-27 Mold release agent for green sand

Country Status (1)

Country Link
JP (1) JP3094115B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5626656A (en) * 1992-12-28 1997-05-06 Tetra Co., Ltd. Stock solution of release agent for green sand mold forming
WO2015064506A1 (en) * 2013-10-28 2015-05-07 トヨタ自動車株式会社 Mold release agent for water glass-containing sand mold molding

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5626656A (en) * 1992-12-28 1997-05-06 Tetra Co., Ltd. Stock solution of release agent for green sand mold forming
WO2015064506A1 (en) * 2013-10-28 2015-05-07 トヨタ自動車株式会社 Mold release agent for water glass-containing sand mold molding
JP6018318B2 (en) * 2013-10-28 2016-11-02 トヨタ自動車株式会社 Mold release agent for sand mold making containing water glass

Also Published As

Publication number Publication date
JP3094115B2 (en) 2000-10-03

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