[go: up one dir, main page]

JPS62142048A - Production of acid curing type organic self-curing sand - Google Patents

Production of acid curing type organic self-curing sand

Info

Publication number
JPS62142048A
JPS62142048A JP28049985A JP28049985A JPS62142048A JP S62142048 A JPS62142048 A JP S62142048A JP 28049985 A JP28049985 A JP 28049985A JP 28049985 A JP28049985 A JP 28049985A JP S62142048 A JPS62142048 A JP S62142048A
Authority
JP
Japan
Prior art keywords
acid
sand
curing
binder
molding sand
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
JP28049985A
Other languages
Japanese (ja)
Other versions
JPH0571335B2 (en
Inventor
Jiyouji Saitou
斎藤 乗史
Isao Kai
勲 甲斐
Kazuo Tamemoto
為本 和雄
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.)
Asahi Yukizai Corp
Original Assignee
Asahi Organic Chemicals Industry Co Ltd
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 Asahi Organic Chemicals Industry Co Ltd filed Critical Asahi Organic Chemicals Industry Co Ltd
Priority to JP28049985A priority Critical patent/JPS62142048A/en
Publication of JPS62142048A publication Critical patent/JPS62142048A/en
Publication of JPH0571335B2 publication Critical patent/JPH0571335B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Mold Materials And Core Materials (AREA)

Abstract

PURPOSE:To prevent casting defects, to reduce the cost of casting and to improve working environment by adding and mixing an acid curing agent to and with org. binder-coated molding sand formed by adding the org. binder to the molding sand. CONSTITUTION:This process is applied to the acid curing type org. self-curing sand of >=5ml/50g, more preferably 10ml/50g acid consumption. A phenolic resin, modified phenolic resin, furan resin or modified furan resin which cures at a room temp. when mixed together with the acid curing agent is used for the org. binder and such binder is added to the molding sand to coat the molding sand. The acid curing agent prepd. by adding a methanol or ethanol to an aq. soln. of an inorg. acid or arom. sulfonic acid is then added and mixed to and with such molding sand. The cost of casting and casting defects are reduced by producing the molding sand in the above-mentioned manner.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は鋳型の作製に用いられる酸硬化型有機自硬性砂
の製造方法に関するものである。さらに詳しくいえば、
本発明は、特に酸消費量の多い鋳物砂の使用において、
硬化性能を大幅に改善した酸硬化型有機自硬性砂を製造
する方法特許するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a method for producing acid-curing organic self-hardening sand used for making molds. In more detail,
The present invention is particularly advantageous when using foundry sand that consumes a large amount of acid.
The company patents a method for producing acid-curing organic self-hardening sand that has significantly improved hardening performance.

従来の技術 従来、常温における鋳型の作製に用いられる酸硬化型有
機自硬性砂としては、通常鋳物砂と、フェノール系LQ
 脂、7ラン系樹脂、フルフリルアルコールなどの有機
系粘結剤と、リン酸や芳香族系スルホン酸などの酸性硬
化剤とを主成分とするものが用いられており、またその
製造については、例えばまず鋳物砂と酸性硬化剤とを充
分に混合し、次いでこの混合物に有機系粘結剤を添加混
合して被覆する方法、あるいは鋳物砂に有機系粘結剤及
び酸性硬化剤を同時に添加混合して被覆する方法などが
一般に採用されている。
Conventional technology Conventionally, acid-curing organic self-hardening sands used for making molds at room temperature are usually foundry sand and phenolic LQ.
The main ingredients used are organic binders such as fat, 7-run resin, and furfuryl alcohol, and acidic curing agents such as phosphoric acid and aromatic sulfonic acids. For example, first, molding sand and an acidic hardener are thoroughly mixed, and then an organic binder is added to this mixture for coating, or an organic binder and an acidic hardener are simultaneously added to the foundry sand. A method of mixing and coating is generally adopted.

しかしなから、鋳物砂として、酸消費量が5 m(!/
S Og(JACT試験法S−4、鋳物砂の酸消費量試
験法)以上のものを用いる場合、前記方法に従って製造
した有機自硬性砂は、硬化速度か極端に遅くなるため、
これを用いて鋳型を作製する場合特に鋳型内部の硬化不
足に伴う造型不良や生産性の低下などの不都合を生じる
However, as foundry sand, the acid consumption is 5 m (!/
When using S Og (JACT Test Method S-4, Acid Consumption Test Method for Foundry Sand), organic self-hardening sand produced according to the above method has an extremely slow curing speed.
When a mold is produced using this, in particular, problems such as poor molding and decreased productivity occur due to insufficient hardening of the inside of the mold.

したがって、このような問題を解決するために、通常酸
性硬化剤を増量したり、あるいはより強酸性の硬化剤を
使用するなどの方法が試みられているが、これらの方法
においても、鋳型コストの上昇や鋳物への浸硫による鋳
造欠陥あるいは酸性硬化剤の熱分解に伴うSO,ガスに
よる作業環境の悪化などの問題は避けられないのが現状
である。
Therefore, in order to solve this problem, methods such as increasing the amount of acidic curing agent or using a stronger acidic curing agent have been tried, but these methods also reduce mold cost. At present, problems such as casting defects due to rising and sulfurization of the casting, and deterioration of the working environment due to SO and gas due to thermal decomposition of the acidic hardening agent are unavoidable.

発明が解決しようとする問題点 本発明の目的は、このような事情に鑑み、酸消費量5 
ml−/ S Og以上の鋳物砂の使用に伴う硬化速度
の低下か効果的(二防止された酸硬化型有磯自硬特許を
提供する二とによって、鋳型の造型不良や生産性の低下
を改善するとともに、鋳型コストの」1昇、浸硫による
鋳造欠陥、SO□ガスによる作業環境の悪化を伴わない
方法を提供することである。
Problems to be Solved by the Invention In view of the above circumstances, the purpose of the present invention is to reduce the amount of acid consumed by 5.
The reduction in hardening speed associated with the use of foundry sand of ml-/S It is an object of the present invention to provide a method that does not involve an increase in mold cost, casting defects due to sulfurization, and deterioration of the working environment due to SO□ gas.

問題点を解決するための手段 本発明者らは前記目的を達成すべく鋭意研究を重ねた結
果、酸硬化型右磯自硬特許を製造するに際し、あらかし
め鋳物砂を有機系粘結剤で被覆し、次いでこれに酸性硬
化剤を配合することにより、その目的を達成しうろこと
を見出し、この知見に基づいて本発明を完成するに至っ
た。
Means for Solving the Problems The inventors of the present invention have conducted intensive research to achieve the above-mentioned object, and as a result, when manufacturing acid-curing type Uiso Jiko Patent, we used pre-coated foundry sand with an organic binder. It was discovered that the objective could be achieved by coating and then adding an acidic curing agent thereto, and based on this knowledge, the present invention was completed.

十なわ九、本発明は、酸消費量5 pi/ 50 g以
上の鋳物砂、有機系粘結剤及1j酸性硬化剤を主成分と
する酸硬化型有(代自硬特許を製造するに当り、まず鋳
物砂に有機系粘結剤を加えて有(幾系粘結剤で被覆した
鋳物砂を形成させ、次いでこれに酸性硬化剤を添加混合
することを特徴とする酸硬化型有磯自硬特許の!!遣方
法を提供するものである。
Nineteenth, the present invention is an acid-curing type molding sand whose main components are foundry sand with an acid consumption of 5 pi/50 g or more, an organic binder, and a 1J acid hardener (in the process of manufacturing the Daijiko patent). , Acid-curing type Aisoji, which is characterized by first adding an organic binder to foundry sand to form foundry sand coated with an organic binder, and then adding and mixing an acid hardener to this. It provides a method for distributing hard patents.

本発明方法1こおいて用いられる鋳物砂は、(社)鋳造
技術普及協会シェルモード部分て・制定された鋳物砂の
酸消費量試験法IAcTAc法5−4)に従って測定さ
れる酸消費量が5 、zn/ 50 g以上、好ましく
は110lN150以上の乙のであり、Sx1150g
未満のものでは本発明の効果は認められない。
The foundry sand used in Method 1 of the present invention has an acid consumption rate measured according to the foundry sand acid consumption test method IAcTAc method 5-4) established by the Foundry Technology Promotion Association Shell Mode Division. 5, zn/ 50g or more, preferably 110lN150 or more, Sx1150g
If it is less than that, the effect of the present invention will not be recognized.

このような鋳物砂としては、例えばグリーンサンドを含
む再生砂、アルカリ性塗型処理中子砂を含む再生砂、C
02砂を含む再生砂、発熱スリーブ残渣を含む再生砂、
ジルコンナンド再土砂、タロマイトサンド再生砂、コー
ルドボックス再生砂、ペプセント再生砂、オリビンサン
ド゛、ツーカー砂などを挙げることができる。
Examples of such foundry sand include recycled sand containing green sand, recycled sand containing alkaline coated core sand, and C.
Recycled sand containing 02 sand, recycled sand containing heat generating sleeve residue,
Examples include recycled zirconand sand, recycled taromite sand, recycled cold box sand, recycled pepcent sand, olivine sand, and Zuker sand.

本発明方法において用いる有機系粘結剤については、酸
性硬化剤とともに混合することによって待(こ加熱する
ことなしに室温で硬化するものであ7tは特に制限はな
く、例えば7エ7−ル樹脂やフラン変性7エ/−ル樹脂
、尿素変性フェノール樹脂、メラミン変性フェノール(
3(脂などの変性フェノールLQ 脂、フラン(31脂
やフェノール変性フラン樹脂、尿素変性7ラン11脂な
どの変性フラン樹脂、フルフリルアルコール、尿素樹脂
及びこれらの混合131脂などの液状樹脂あるいはモア
マーか用いられる。また、該粘結剤には接着性及び耐湿
性を向トさせるためのシリコーン系やナタネート系、あ
るいはその池のカンプリング剤、脂肪酸アマイドなどの
離型剤、尿素やグアニジノなどのホルムアルデヒド捕捉
剤などの公知物質を添加することができる。
The organic binder used in the method of the present invention is one that cures at room temperature without heating by mixing with an acidic curing agent. Furan-modified 7-el resin, urea-modified phenol resin, melamine-modified phenol (
3 (modified phenol LQ such as fat) fat, furan (31 fat, phenol-modified furan resin, modified furan resin such as urea-modified 7 run 11 fat, furfuryl alcohol, urea resin, and liquid resin such as 131 fat, a mixture of these fats, etc.) In addition, the binder may contain silicone-based or nathanate-based camping agents, mold release agents such as fatty acid amide, urea, guanidino, etc. to improve adhesiveness and moisture resistance. Known substances such as formaldehyde scavengers can be added.

本発明方法において用いる酸硬化剤としては、例えばリ
ン酸、硫酸、ルイス酸などの無機酸、パラトルエンスル
ホン酸、ベンセ′ン又ルホン酸、フェノールスルホン酸
、キシレンスルホン酸などの芳香族スルホン酸、又はこ
れらの混合物などを挙げることができる。このような酸
硬化剤は通常、水溶液又は水溶液(こメタノールやエタ
ノールなどを適当量加えた混合溶液として使用される。
Examples of acid curing agents used in the method of the present invention include inorganic acids such as phosphoric acid, sulfuric acid, and Lewis acids; aromatic sulfonic acids such as p-toluenesulfonic acid, benzene or sulfonic acid, phenolsulfonic acid, and xylene sulfonic acid; or a mixture thereof. Such acid curing agents are usually used as an aqueous solution or a mixed solution containing an appropriate amount of methanol, ethanol, etc.

また、本発明における酸硬化型有[幾自硬特許には、前
記成分以外に必要に応して従来一般的に使用されている
添加剤、例えば硬化促進剤、砂鉄、ベン〃う、木粉など
を配合することらできる。前記硬化促進剤としては、例
えばレゾルシノール、キシレ/−ル、カテコール、クレ
ゾール、ビス7エ7−ルF、ビスフェ/−ルへなどか用
いられる。
In addition to the above-mentioned ingredients, additives commonly used in the past, such as curing accelerators, iron sand, benzene, and wood flour, are also included in the acid-curing type patent of the present invention. It is also possible to combine the following. Examples of the curing accelerator include resorcinol, xylene/ol, catechol, cresol, bis-7er-F, and bispherol.

作用 本発明方法により得られる酸硬化型有機自硬性砂におい
ては、酸消費量5zN150g以上の鋳物砂を用いてい
るにもかかわらず、硬化阻害が防止される特徴を有して
いる。この硬化阻害防止のメカニズムについては必ずし
も明確ではないが、次のように推察される。
Function The acid-curing type organic self-hardening sand obtained by the method of the present invention has the characteristic that hardening inhibition is prevented even though foundry sand with an acid consumption of 5 zN or more is used. Although the mechanism of preventing this curing inhibition is not necessarily clear, it is inferred as follows.

すなわち、前記鋳物砂は本発明方法に従ってまず有機系
粘結剤で被覆されて、該鋳物砂の表面に該粘結剤の薄膜
か形成されるため、次に添加される酸性硬化剤との接触
が防止され、その結果、該硬化剤と該鋳物砂表面ないし
はそれに含有される塩基性成分との中和反応が阻害され
て、該硬化剤が消貸されないことから、健全な硬化機能
が付与されるものと考えられる。
That is, the foundry sand is first coated with an organic binder according to the method of the present invention, and a thin film of the binder is formed on the surface of the foundry sand, which prevents contact with the acidic curing agent added next. As a result, the neutralization reaction between the hardening agent and the surface of the foundry sand or the basic components contained therein is inhibited, and since the hardening agent is not used up, a sound hardening function is imparted. It is considered that

実施例 次に実施例及び比較例によl)本発明をさらに詳細に説
明する。なお、ここに記載されている「部」及び「%」
は特に断りのないかぎりすべて重量基準である。
EXAMPLES Next, the present invention will be explained in further detail with reference to Examples and Comparative Examples. In addition, "part" and "%" written here
All values are by weight unless otherwise specified.

実施例1及び比較例1〜2 カルサイカー焙焼法によって再生したノルコン再生砂(
酸消費量25zN150i?粒度指数(八FS)100
)3000部とフェノールフラン樹脂、AVライトII
P100OF(旭有磯材工業(株)製)54部を品用式
卓上ミキサーに入れ、30秒間かきまぜ混合して樹脂被
覆砂とし、引続と酸性硬化剤として芳香族系スルホン酸
水;3液AVライ) I”13−20(旭有磯材工業(
株)製)22部を添加し、さらに30秒間混合してから
取り出す本発明方法に従って常温自硬性混練砂を調製し
た。
Example 1 and Comparative Examples 1 and 2 Norcon recycled sand (
Acid consumption 25zN150i? Particle size index (8FS) 100
) 3000 parts and phenolfuran resin, AV Light II
Put 54 parts of P100OF (manufactured by Asahi Ariisozai Kogyo Co., Ltd.) into a tabletop mixer, stir and mix for 30 seconds to obtain resin-coated sand, and then add aromatic sulfonic acid water as an acidic curing agent; 3-part AV Rai) I”13-20 (Asahi Ariisozai Kogyo (
A room-temperature self-hardening kneaded sand was prepared according to the method of the present invention, in which 22 parts of (manufactured by) Co., Ltd.) were added, mixed for an additional 30 seconds, and then taken out.

得られた前記混練砂は、ただちに多数の抗圧力試験片(
径50Il!I×高さ5ozjI)を同時に作製可能な
木型に手込め充填して室温に放置した。その後、所定経
過時間ごとに抜型してその強度(抗圧力)を測定し、硬
化挙動については、初期強度(経過時間0.5〜3時間
)の挙動により、また鋳型の終結強度については24時
間経過後の強度によって優劣を判定した。
The obtained kneaded sand was immediately subjected to a large number of anti-pressure test pieces (
Diameter 50Il! I×height 5 oz. Thereafter, the mold was removed at predetermined elapsed time intervals and its strength (resistance pressure) was measured.The hardening behavior was measured based on the behavior of the initial strength (elapsed time 0.5 to 3 hours), and the final strength of the mold was measured after 24 hours. Superiority or inferiority was determined based on the strength after the test.

併せて本発明方法と対照比較のため、フェノールフラン
樹脂と酸性硬化剤の添加順序を逆にする以外は前記実施
例1に従った従来方法Aを比較例1とし、またフェノー
ルフラン樹脂と酸性硬化剤を同時に添加混合する以外は
上記実施例1に従った池の従来方法Bを比較例2とした
。その結果を第1表に併せ記載する。
In addition, for comparison with the method of the present invention, conventional method A according to Example 1 was used as Comparative Example 1, except that the order of addition of the phenol furan resin and the acidic curing agent was reversed, and the phenolfuran resin and the acidic curing agent were Comparative Example 2 was the conventional method B of the pond according to Example 1 except that the agent was added and mixed at the same time. The results are also listed in Table 1.

第1表 (注)混合方法 (イ)発明方法 粘結剤 (ロ)従来方法A 硬化剤 (ハ)従来方法B 砂十粘結剤+硬化剤 実施例2〜4及び比較例3〜10 第2表の配合欄に記載される鋳物砂、有機系粘結剤及び
酸性硬化剤を用いる以外は、それぞれ実施例1、比較例
1又は比較例2に従って常温自硬性混練砂を調製したの
ち、前記方法によって該混練砂の硬化挙動及び鋳型の終
結強度を求めた。その結果を第2表に記載する。
Table 1 (Note) Mixing method (a) Inventive method Binder (b) Conventional method A Curing agent (c) Conventional method B Binder + curing agent Examples 2 to 4 and Comparative Examples 3 to 10 Room-temperature self-hardening kneaded sand was prepared according to Example 1, Comparative Example 1, or Comparative Example 2, respectively, except for using the foundry sand, organic binder, and acid hardener listed in the formulation column of Table 2. The hardening behavior of the mixed sand and the final strength of the mold were determined by the method. The results are listed in Table 2.

発明の効果 以上の説明から明らかなように、酸消費量が5m/11
50g以上の鋳物砂を用いて酸硬化型有磯自硬消費を製
造するに際し、本発明方法に従えば、その硬化性能が大
幅に向上するために、鋳型内部の硬化不足に伴う造型不
良や生産性の低下が防止され、また、酸性硬化剤を増量
したり、あるいはより強酸性の硬化剤を使用したりする
必要がなくなるため、鋳型コストの上昇、浸硫による鋳
物の鋳造欠陥、SO。ガスによる作業環境の悪化などの
諸問題を解決することができる。
Effects of the invention As is clear from the above explanation, acid consumption is 5 m/11
When manufacturing acid-cured Aiso self-hardened moldings using 50g or more of foundry sand, if the method of the present invention is followed, the curing performance will be greatly improved, thereby reducing molding defects and production due to insufficient hardening inside the mold. In addition, it is not necessary to increase the amount of acidic curing agent or use a stronger acidic curing agent, which eliminates the need for increased mold costs, casting defects in castings due to sulfurization, and SO. Various problems such as deterioration of the working environment due to gas can be solved.

Claims (1)

【特許請求の範囲】[Claims] 1 酸消費量5ml/50g以上の鋳物砂、有機系粘結
剤及び酸性硬化剤を主成分とする酸硬化型有機自硬性砂
を製造するに当り、まず鋳物砂に有機系粘結剤を加えて
、有機系粘結剤で被覆した鋳物砂を形成させ、次いでこ
れに酸性硬化剤を添加混合することを特徴とする酸硬化
型有機自硬性砂の製造方法。
1. When producing acid-curing organic self-hardening sand whose main components are foundry sand with an acid consumption of 5 ml/50 g or more, an organic binder, and an acidic hardener, first add an organic binder to the foundry sand. 1. A method for producing acid-curing organic self-hardening sand, which comprises forming foundry sand coated with an organic binder, and then adding and mixing an acid curing agent thereto.
JP28049985A 1985-12-13 1985-12-13 Production of acid curing type organic self-curing sand Granted JPS62142048A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP28049985A JPS62142048A (en) 1985-12-13 1985-12-13 Production of acid curing type organic self-curing sand

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP28049985A JPS62142048A (en) 1985-12-13 1985-12-13 Production of acid curing type organic self-curing sand

Publications (2)

Publication Number Publication Date
JPS62142048A true JPS62142048A (en) 1987-06-25
JPH0571335B2 JPH0571335B2 (en) 1993-10-07

Family

ID=17625937

Family Applications (1)

Application Number Title Priority Date Filing Date
JP28049985A Granted JPS62142048A (en) 1985-12-13 1985-12-13 Production of acid curing type organic self-curing sand

Country Status (1)

Country Link
JP (1) JPS62142048A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101992260A (en) * 2010-11-05 2011-03-30 中国第一汽车集团公司 Furan self-hardening resin sand mold for producing integral casting axle case
CN105108045A (en) * 2015-08-11 2015-12-02 安徽省胜峰机械有限公司 Chopped carbon fiber containing and reinforced type modified furan resin sand for steel casting and preparation method of resin sand
CN105108032A (en) * 2015-08-11 2015-12-02 安徽省胜峰机械有限公司 High-plasticity modified furan resin sand for steel casting and preparation method of high-plasticity modified furan resin sand
CN105499497A (en) * 2015-12-30 2016-04-20 青岛博泰美联化工技术有限公司 V-method casting process
JP2017100162A (en) * 2015-12-02 2017-06-08 ダイハツ工業株式会社 Sand mold manufacturing method and sand mold
CN110290886A (en) * 2017-02-28 2019-09-27 大发工业株式会社 The manufacturing method and molding sand of molding sand

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101992260A (en) * 2010-11-05 2011-03-30 中国第一汽车集团公司 Furan self-hardening resin sand mold for producing integral casting axle case
CN105108045A (en) * 2015-08-11 2015-12-02 安徽省胜峰机械有限公司 Chopped carbon fiber containing and reinforced type modified furan resin sand for steel casting and preparation method of resin sand
CN105108032A (en) * 2015-08-11 2015-12-02 安徽省胜峰机械有限公司 High-plasticity modified furan resin sand for steel casting and preparation method of high-plasticity modified furan resin sand
JP2017100162A (en) * 2015-12-02 2017-06-08 ダイハツ工業株式会社 Sand mold manufacturing method and sand mold
CN105499497A (en) * 2015-12-30 2016-04-20 青岛博泰美联化工技术有限公司 V-method casting process
CN110290886A (en) * 2017-02-28 2019-09-27 大发工业株式会社 The manufacturing method and molding sand of molding sand
EP3590626A4 (en) * 2017-02-28 2020-11-18 Daihatsu Motor Co., Ltd. Method for producing casting sand, and casting sand
US11590561B2 (en) 2017-02-28 2023-02-28 Daihatsu Motor Co., Ltd. Method of producing sand mold comprising curing a resin and a binder by the same curing agent

Also Published As

Publication number Publication date
JPH0571335B2 (en) 1993-10-07

Similar Documents

Publication Publication Date Title
JPH02500753A (en) Modifier for aqueous base solution of phenolic resol resin
JPS62142048A (en) Production of acid curing type organic self-curing sand
JP2008023529A (en) Furan resin composition for making casting mold
US4766949A (en) Hot box process for preparing foundry shapes
JP2013107135A (en) Elimination of odors in shell sand encapsulation
JPS6131737B2 (en)
US3138836A (en) Foundry molds and cores and process for making same
CN114163210B (en) Self-hardening curing agent and preparation method thereof
JPS5948062B2 (en) How to cure binder
JP2542144B2 (en) Binder composition for organic ester-curable foundry sand and method for producing mold using the same
JPH02299741A (en) Improvement of fluidity of resin-coated sand
JP3131640B2 (en) Binder composition for mold production and method for producing mold
SU1572737A1 (en) Sand for making cores and moulds with hot hardening
JP3131639B2 (en) Binder composition for heat-curing mold and method for producing mold
JPH02197348A (en) Resin coated sand particles for hot box
JP2593332B2 (en) Resin-coated sand composition for hot box
JP3457188B2 (en) Hardener composition for mold production
JP2000102840A (en) Casting mold manufacturing method
JPS60145238A (en) Peroxide composition for casting mold
JPS5832539A (en) Composition for molding sand
JPH06179044A (en) Binder composition for gas curing casting mold and production of casting mold
JPS6142449A (en) Molding method of sand mold
RU1799658C (en) Clad mixture for manufacture of casting molds and cores
JPS61245937A (en) Compound for casting mold material
SU876256A1 (en) Binder for making cores and moulds