JP2000102842A - Mold molding composition and mold molding method - Google Patents
Mold molding composition and mold molding methodInfo
- Publication number
- JP2000102842A JP2000102842A JP10274707A JP27470798A JP2000102842A JP 2000102842 A JP2000102842 A JP 2000102842A JP 10274707 A JP10274707 A JP 10274707A JP 27470798 A JP27470798 A JP 27470798A JP 2000102842 A JP2000102842 A JP 2000102842A
- Authority
- JP
- Japan
- Prior art keywords
- mold
- weight
- water
- mold molding
- parts
- 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.)
- Pending
Links
Landscapes
- Mold Materials And Core Materials (AREA)
Abstract
Description
【産業上の利用分野】本発明は、常温ガス硬化鋳型造型
法において、鋳型造型時の作業環境を改善し、かつ高強
度で高品質な鋳型が得られる、鋳型造型用組成物及び鋳
型造型方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a room temperature gas-curing mold molding method, which improves the working environment during mold molding and provides a high-strength, high-quality mold. About.
【従来の技術】従来、鋳造用鋳型の製造方法として、ポ
リオール化合物とポリイソシアネート化合物を粒状耐火
性骨材と混合し、これを型枠内に導入して成型した後、
第三級アミンガスを通気して硬化させ、鋳型を得る、い
わゆるアミンコールドボックス法がある。この方法で
は、製造に際して加熱を必要としない為にエネルギー消
費の点で有利であり、また、造型サイクルが短く生産性
が高いという利点がある。しかしながら、従来技術では
触媒としてアミンガスを大量に使用しなくてはならず、
これが作業環境を悪化させている。また、アミン量を少
なくすると、鋳型強度が大きく低下し、十分なハンドリ
ング強度が得られず、さらに、鋳型の品質も悪くなり、
そのため鋳物欠陥が発生してしまうという欠点がある。2. Description of the Related Art Conventionally, as a method of manufacturing a casting mold, a polyol compound and a polyisocyanate compound are mixed with a granular refractory aggregate, and the mixture is introduced into a mold and molded.
There is a so-called amine cold box method in which a tertiary amine gas is aerated and cured to obtain a mold. This method is advantageous in terms of energy consumption because heating is not required for production, and has the advantage that the molding cycle is short and the productivity is high. However, in the prior art, a large amount of amine gas must be used as a catalyst,
This is deteriorating the working environment. In addition, when the amount of amine is reduced, the strength of the mold is greatly reduced, sufficient handling strength is not obtained, and the quality of the mold is deteriorated.
Therefore, there is a drawback that casting defects occur.
【課題を解決するための手段】上記のような欠点を解消
するべく、鋭意研究した結果、第三級アミン、アルコー
ル類及び/又は水の混合ガスを使用することにより、ア
ミン使用量を大幅に低減し、なおかつ高い鋳型強度を有
する鋳型を得ることに成功し、本発明を完成するに至っ
た。従来技術では、キュアリング時、水蒸気の混入は強
度劣化を招くために避けるべきであるとされてきた。し
かし、本発明の技術を用いれば、逆に鋳型強度を大幅に
向上させることが可能である。すなわち、アミンガス通
気時、同時にアルコール類及び/又は水の混合ガスを通
気する事により、フェノール樹脂とイソシアネート樹脂
の硬化反応が促進され、鋳型強度は向上する。以下、本
発明を詳細に記述する。本発明は、ポリオール化合物、
ポリイソシアネート化合物を含む粘結剤により被覆され
た粒状耐火性骨材を型枠内に導入して成型し、次いで前
記型枠内に硬化促進剤をガス化して導入し硬化させる鋳
型の製造方法において、使用される効果促進剤が第三級
アミンとアルコール類及び/又は水を含有した混合溶液
であることを特徴とする鋳型造型用組成物、及び硬化促
進ガスが第三級アミンとアルコール類及び/又は水を含
有した混合ガスであることを特徴とする、鋳型造型方法
である。本発明で用いられるアルコール類としては、メ
タノール、エタノール、プロパノール、ブタノール等が
ある。第三級アミンとしては、トリエチルアミン、ジメ
チルエチルアミン等を用いることができる。第三級アミ
ン、アルコール類及び水の混合割合は任意であるが、ア
ミンの低減と鋳型の高強度化の両立の観点から、混合ガ
ス中のアルコール類及び/又は水の合計の濃度が20〜
95重量%であることがより好ましい。Means for Solving the Problems As a result of intensive studies to solve the above-mentioned drawbacks, the use of a mixed gas of tertiary amine, alcohols and / or water has greatly reduced the amount of amine used. The inventors succeeded in obtaining a mold having reduced mold strength and high mold strength, and completed the present invention. In the prior art, it has been suggested that during curing, the incorporation of water vapor should be avoided to cause deterioration in strength. However, by using the technique of the present invention, it is possible to greatly improve the strength of the mold. That is, by simultaneously passing the mixed gas of alcohols and / or water when the amine gas is passed, the curing reaction between the phenol resin and the isocyanate resin is promoted, and the mold strength is improved. Hereinafter, the present invention will be described in detail. The present invention provides a polyol compound,
In a method for producing a mold, a granular refractory aggregate coated with a binder containing a polyisocyanate compound is introduced into a mold and molded, and then a curing accelerator is gasified and introduced into the mold and cured. Wherein the effect accelerator used is a mixed solution containing a tertiary amine and an alcohol and / or water, and the curing accelerator gas is a tertiary amine and an alcohol; And / or a mixed gas containing water. The alcohols used in the present invention include methanol, ethanol, propanol, butanol and the like. As the tertiary amine, triethylamine, dimethylethylamine and the like can be used. The mixing ratio of the tertiary amine, the alcohol and the water is arbitrary, but from the viewpoint of reducing the amine and increasing the strength of the template, the total concentration of the alcohol and / or water in the mixed gas is from 20 to
More preferably, it is 95% by weight.
【実施例】以下、実施例をあげて本発明に係る鋳型造型
方法を更に詳しく説明する。但し、本発明は、下記実施
例に限定されるものではなく、その要旨の範囲内で種々
変形実施が可能である。 [実施例1]フェノール800重量部、86%ホルムア
ルデヒド445重量部、トルエン200重量部を還流脱
水装置を備えたセパラブルフラスコに仕込み、次いで酢
酸亜鉛を8重量部加え、100〜130℃の温度範囲に
て還流脱水反応を4時間続けた。更にその後、真空下で
縮合水及び溶剤を除去し、冷却した。生成物をIR及びNM
Rで分析したところ、ベンジリックエーテル型フェノー
ル樹脂であることを確認した。反応生成物にエチレング
リコールジアセテートと芳香族溶剤(丸善石油化学株式
会社製 商品名スワゾール)との1:1の混合溶剤15
79重量部を添加混合して、ポリオール化合物溶液27
70重量部を得た。次に、ジフェニルメタンジイソシア
ネート2216重量部にスワゾール554重量部を添加
混合し、ポリイソシアネート化合物溶液2770重量部
を得た。次に、トリエチルアミン200重量部とイソプ
ロパノール100重量部、水200重量部を混合し、硬
化促進溶液500重量部を得た。次に、飯豊F6号珪砂1
000重量部に対し上記のポリオール化合物溶液10重
量部、ポリイソシアネート化合物溶液10重量部を混練
し、混練砂を得た。該混練砂を20×20×150mmの
テストピース5個取り金型にブロー圧2kgf/cm2で吹き
込んだ後、上記硬化促進溶液を混練砂に対し1.5重量
部気化させて金型内に導入させ、硬化鋳型を得た。この
時、硬化直後及び24時間後の抗折力を測定した。ま
た、造型機の周囲5mの範囲にパネラー10人を配置し
造型時の臭気の官能試験を実施した。結果を表1に示
す。 [実施例2]トリエチルアミン200重量部とメタノー
ル50重量部、水250重量部を混合し、硬化促進溶液
500重量部を得た。次に、実施例1で得られた混練砂
を実施例1と同様に金型内に吹き込み、上記硬化促進溶
液を混練砂に対し1.5重量部気化させて金型内に導入
させ、硬化鋳型を得た。実施例1と同様の試験を実施し
た。 [実施例3]実施例1で得られた混練砂を実施例1と同
様に金型内に吹き込み、実施例1で得られた硬化促進溶
液を混練砂に対し1.0重量部気化させて金型内に導入
させ、硬化鋳型を得た。実施例1と同様の試験を実施し
た。 [比較例1]実施例1で得られた混練砂を実施例1と同
様に金型内に吹き込み、トリエチルアミンを混練砂に対
し1.5重量部気化させて金型内に導入させ、硬化鋳型
を得た。実施例1と同様の試験を実施した。EXAMPLES Hereinafter, the mold making method according to the present invention will be described in more detail with reference to examples. However, the present invention is not limited to the following embodiments, and various modifications can be made within the scope of the gist. [Example 1] 800 parts by weight of phenol, 445 parts by weight of 86% formaldehyde and 200 parts by weight of toluene were charged into a separable flask equipped with a reflux dehydrator, and then 8 parts by weight of zinc acetate was added. The reflux dehydration reaction was continued for 4 hours. Thereafter, the condensed water and the solvent were removed under vacuum, and the mixture was cooled. IR and NM products
Analysis by R confirmed that the resin was a benzylic ether type phenol resin. A 1: 1 mixed solvent of ethylene glycol diacetate and an aromatic solvent (manufactured by Maruzen Petrochemical Co., Ltd. under the trade name Swazole) as the reaction product 15
79 parts by weight of the polyol compound solution 27 were mixed.
70 parts by weight were obtained. Next, 554 parts by weight of swazole was added to 2216 parts by weight of diphenylmethane diisocyanate and mixed to obtain 2770 parts by weight of a polyisocyanate compound solution. Next, 200 parts by weight of triethylamine, 100 parts by weight of isopropanol, and 200 parts by weight of water were mixed to obtain 500 parts by weight of a curing acceleration solution. Next, Iide F6 quartz sand 1
10 parts by weight of the above polyol compound solution and 10 parts by weight of the polyisocyanate compound solution were kneaded with respect to 000 parts by weight to obtain kneaded sand. The kneading sand was blown into a mold for taking five test pieces of 20 × 20 × 150 mm at a blow pressure of 2 kgf / cm 2 , and then the hardening accelerating solution was vaporized to 1.5 parts by weight with respect to the kneading sand. And a cured mold was obtained. At this time, the transverse rupture force was measured immediately after curing and 24 hours later. In addition, 10 panelists were placed in a range of 5 m around the molding machine, and a sensory test of odor during molding was performed. Table 1 shows the results. [Example 2] 200 parts by weight of triethylamine, 50 parts by weight of methanol and 250 parts by weight of water were mixed to obtain 500 parts by weight of a curing acceleration solution. Next, the kneaded sand obtained in Example 1 was blown into a mold in the same manner as in Example 1, and the hardening promoting solution was vaporized to 1.5 parts by weight with respect to the kneaded sand, introduced into the mold, and cured. A mold was obtained. The same test as in Example 1 was performed. [Example 3] The kneaded sand obtained in Example 1 was blown into a mold in the same manner as in Example 1, and the hardening accelerating solution obtained in Example 1 was vaporized to 1.0 part by weight with respect to the kneaded sand. It was introduced into a mold to obtain a cured mold. The same test as in Example 1 was performed. [Comparative Example 1] The kneaded sand obtained in Example 1 was blown into a mold in the same manner as in Example 1, and 1.5 parts by weight of triethylamine was vaporized with respect to the kneaded sand, and introduced into the mold. I got The same test as in Example 1 was performed.
【表1】 [Table 1]
【発明の効果】上述のように、本発明の鋳型造型用組成
物及び鋳型造型方法を用いることにより、鋳型造型時の
作業環境を改善し、かつ高強度で高品質な鋳型を得るこ
とができる。As described above, by using the composition for mold making and the method for mold making of the present invention, the working environment at the time of mold making can be improved, and a high-strength, high-quality mold can be obtained. .
───────────────────────────────────────────────────── フロントページの続き (72)発明者 糸澤 利明 群馬県高崎市宿大類町700番地 群栄化学 工業株式会社内 (72)発明者 栗本 好章 群馬県高崎市宿大類町700番地 群栄化学 工業株式会社内 Fターム(参考) 4E092 AA23 AA31 AA32 AA55 BA04 BA12 CA03 ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Toshiaki Itozawa 700 Shukudaidaicho, Takasaki City, Gunma Prefecture Inside Gunei Chemical Industry Co., Ltd. Co., Ltd. F-term (reference) 4E092 AA23 AA31 AA32 AA55 BA04 BA12 CA03
Claims (5)
合物を含む粘結剤により被覆された粒状耐火性骨材を型
枠内に導入して成型し、次いで前記型枠内に硬化促進剤
をガス化して導入し硬化させる鋳型の製造方法におい
て、使用される効果促進剤が第三級アミンとアルコール
類及び/又は水を含有した混合溶液であることを特徴と
する、鋳型造型用組成物。1. A particulate refractory aggregate coated with a binder containing a polyol compound and a polyisocyanate compound is introduced into a mold and molded, and then a curing accelerator is gasified and introduced into the mold. A method for producing a mold, wherein the effect accelerator used is a mixed solution containing a tertiary amine, alcohols and / or water.
ール類及び/又は水の合計の濃度が20〜95重量%で
あることを特徴とする、請求項1記載の鋳型造型用組成
物。2. The composition according to claim 1, wherein the curing accelerator has a total concentration of alcohols and / or water in the solution of 20 to 95% by weight.
合物を含む粘結剤により被覆された粒状耐火性骨材を型
枠内に導入して成型し、次いで前記型枠内に硬化促進ガ
スを導入して硬化させる鋳型の製造方法において、前記
硬化促進ガスが第三級アミンとアルコール類及び/又は
水を含有した混合ガスであることを特徴とする、鋳型造
型方法。3. A granular refractory aggregate coated with a binder containing a polyol compound and a polyisocyanate compound is introduced into a mold, molded, and then cured by introducing a curing accelerating gas into the mold. A method for producing a mold, wherein the curing-acceleration gas is a mixed gas containing a tertiary amine, an alcohol, and / or water.
アルコール類及び/又は水の合計の濃度が20〜95重
量%であることを特徴とする、請求項3記載の鋳型造型
方法。4. The method according to claim 3, wherein the total concentration of alcohols and / or water in the mixed gas is 20 to 95% by weight.
合物を含む粘結剤により被覆された粒状耐火性骨材を型
枠内に導入して成型し、次いで前記型枠内に硬化促進ガ
スを導入して硬化させる鋳型の製造方法において、前記
硬化促進ガスが第三級アミンとアルコール類及び/又は
水を含有した混合溶液をガス化することにより得られる
ことを特徴とする、鋳型造型方法。5. A granular refractory aggregate coated with a binder containing a polyol compound and a polyisocyanate compound is introduced into a mold, molded, and then cured by introducing a curing accelerating gas into the mold. A method for producing a mold, wherein the curing accelerating gas is obtained by gasifying a mixed solution containing a tertiary amine and an alcohol and / or water.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10274707A JP2000102842A (en) | 1998-09-29 | 1998-09-29 | Mold molding composition and mold molding method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10274707A JP2000102842A (en) | 1998-09-29 | 1998-09-29 | Mold molding composition and mold molding method |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2000102842A true JP2000102842A (en) | 2000-04-11 |
Family
ID=17545450
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10274707A Pending JP2000102842A (en) | 1998-09-29 | 1998-09-29 | Mold molding composition and mold molding method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2000102842A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7517922B2 (en) * | 2001-10-30 | 2009-04-14 | Wyman Ransome J | Roadway repair and maintenance |
-
1998
- 1998-09-29 JP JP10274707A patent/JP2000102842A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7517922B2 (en) * | 2001-10-30 | 2009-04-14 | Wyman Ransome J | Roadway repair and maintenance |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101199982A (en) | Low sulfur curing agent for furan resin casting | |
WO2009150983A1 (en) | Manufacturing method for phenolic novolac resin and resin‑coated sand | |
FI90020B (en) | Foundry resin | |
CN110079049A (en) | A kind of sheet molding material resin composition, sheet molding compound and preparation method thereof | |
US4224201A (en) | Foundry binders | |
CN110252939A (en) | A kind of sand mold mould regenerating resin sand and its preparation process | |
JP2000102842A (en) | Mold molding composition and mold molding method | |
JPS583779B2 (en) | Manufacturing method for water-soluble molds | |
JP3698445B2 (en) | Catalytic curing agent for resin and method for producing the same | |
US3839265A (en) | Polymeric composition and method | |
US4066588A (en) | Cold-curing binder for foundry sand cores and molds | |
US20040051078A1 (en) | Reactive amine catalysts for use in PUCB foundry binder | |
JPH09234540A (en) | Binder coated sand grain for mold | |
JPS6114042A (en) | Production of casting mold | |
JPS5846377B2 (en) | Binder composition for foundry sand | |
US20050176845A1 (en) | Core material | |
CS210647B2 (en) | Foundry mould or core,manufactured from quocksetting sand mixture | |
JP3169456B2 (en) | Mold production method | |
CN113388088A (en) | Polyurethane material for antistatic plate for electronic test | |
US1146388A (en) | Process for making sound-records. | |
CN101544506B (en) | Raw material formula of tundish insulating board and preparation method for tundish insulating board | |
JPS6114043A (en) | Resin-coated sand curable by heating for casting and its production | |
JPH04294839A (en) | Binder for molding sand and its manufacture | |
JPS57206549A (en) | Binder composition for molding sand | |
JPH06328189A (en) | Production of casting mold |