JPS6234645A - Production of sand mold for casting - Google Patents
Production of sand mold for castingInfo
- Publication number
- JPS6234645A JPS6234645A JP17524685A JP17524685A JPS6234645A JP S6234645 A JPS6234645 A JP S6234645A JP 17524685 A JP17524685 A JP 17524685A JP 17524685 A JP17524685 A JP 17524685A JP S6234645 A JPS6234645 A JP S6234645A
- Authority
- JP
- Japan
- Prior art keywords
- sand
- maleic anhydride
- hydrolyzate
- butadiene
- sand mold
- 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
【発明の詳細な説明】
3、発明の訂Illな説明
[産業上の利用分野]
本発明は鋳物川砂をの製造法に関する。更に詳しくはp
H5以下のブタジェン/無水マレイン酸共重合体の加水
分解物のアルカリまたはアルカリ土類金属塩の水溶液を
、鋳物砂100重量部に対して該加水分解物の金属塩が
0.1〜5重量部となるように鋳物砂と混合して、成形
後加熱乾燥して硬化せしめることを特徴とする鋳物川砂
をの製造法に関する。Detailed Description of the Invention 3. Revised Description of the Invention [Field of Industrial Application] The present invention relates to a method for producing river sand for casting. For more details, see p.
An aqueous solution of an alkali or alkaline earth metal salt of a hydrolyzate of a butadiene/maleic anhydride copolymer of H5 or less is mixed with 0.1 to 5 parts by weight of the metal salt of the hydrolyzate per 100 parts by weight of foundry sand. The present invention relates to a method for producing foundry river sand, which is characterized in that it is mixed with foundry sand so as to have the following properties, and then heated and dried after molding to harden it.
[従来技術とその問題点]
従来、鋳物用の砂型を製造するには、ケイ砂などの鋳物
砂に無機物質あるいは有機物質のバインダーを配合し、
成形、硬化させて行なっている。[Prior art and its problems] Conventionally, in order to manufacture sand molds for foundries, an inorganic or organic binder is mixed with foundry sand such as silica sand,
This is done by molding and curing.
その際、これらの各種のバインダーには、それぞれ一長
一短がある。In this case, each of these various binders has advantages and disadvantages.
例えば水ガラスの場合、使用済みの砂型を廃棄すると、
砂の表面に固着している水ガラスがアルカリ性のため、
廃棄周辺の土壌を汚染することがある。このような公害
上の問題から、水ガラスに代る鋳物砂川バインダーの開
発が要望されている。For example, in the case of water glass, if you discard the used sand mold,
Because the water glass that adheres to the sand surface is alkaline,
It may contaminate the soil around the disposal. Due to such pollution problems, there is a demand for the development of a cast iron Sunagawa binder to replace water glass.
その一つの解決策として、自硬性のフラン樹脂あるいは
フェノール樹脂を原料とする有機バインダーが注目され
ている。これらの有機バインダーは使用後に砂を粉砕、
摩擦あるいは燃焼することにより、有機バインダーが除
去されるので、鋳物砂が再利用できる利点がある。しか
しながら粉砕、摩擦などによる操作は面倒であり、また
燃焼時に悪臭を発するなどの欠点がある。さらに鋳物砂
の性質、含水量、温度、湿度、硬化剤として使用する酸
の種類、およびその11度などの要因によりバインダー
の硬化速度、砂型の機械的強度が著しく異なり取扱いが
困難である。またバインダー原料は保存中に次第に重合
が促進されるので、製造後−年以内に潤賀しな【プれば
ならないという欠点があった。有機バインダーとしてこ
のほかにイソブチレンなどのα−オレフィンと無水マレ
イン酸との共重合体も提案されている。このような無水
マレイン酸などを用いた水溶性ポリマーは、上述の欠点
を解消するだけでなく、鋳型再生の容易さ、種々の他の
ポリマーとの混合の容易さなどの点からイj望祝されて
いる。しかしながら、上記の共重合体からなるバインダ
ーを用いる方法では、大きな強度を右づ゛る砂型は得ら
れず、高品質・高精度の鋳物が要求されている現在、中
形や大型の砂型、J3よび高い精度を要求される鋳物用
の砂型には、上述の欠点の改良を望みつつ、あえてフラ
ン樹脂等の自硬性の有機バインダーが用いられている。As one solution to this problem, organic binders made from self-hardening furan resins or phenolic resins are attracting attention. These organic binders crush the sand after use,
Since the organic binder is removed by friction or combustion, there is an advantage that the foundry sand can be reused. However, operations such as crushing and friction are troublesome, and they also have drawbacks such as emitting a bad odor when burned. Furthermore, the hardening speed of the binder and the mechanical strength of the sand mold vary significantly depending on factors such as the properties of the foundry sand, water content, temperature, humidity, type of acid used as a hardening agent, and its temperature of 11 degrees, making handling difficult. Furthermore, since the polymerization of the binder raw material is gradually accelerated during storage, it has the disadvantage that it must be washed within a year after production. Copolymers of α-olefins such as isobutylene and maleic anhydride have also been proposed as organic binders. Such water-soluble polymers using maleic anhydride and the like not only eliminate the above-mentioned drawbacks, but also are desirable because they are easy to regenerate molds and are easy to mix with various other polymers. has been done. However, with the method of using a binder made of the copolymer described above, it is not possible to obtain a sand mold with great strength.Nowadays, when high-quality and high-precision castings are required, medium-sized and large-sized sand molds, J3 In sand molds for castings, which require high precision, self-hardening organic binders such as furan resins are intentionally used in hopes of improving the above-mentioned drawbacks.
[問題点を解決する手段]
本発明の目的は、上述した従来提案の鋳物用砂型の製造
法の欠点を解消した新規な方法を提案でることにある。[Means for Solving the Problems] An object of the present invention is to propose a new method that eliminates the drawbacks of the above-mentioned conventional methods for manufacturing foundry sand molds.
すなわら本発明によって得られる砂型は、従来提案され
てきた無水マレイン酸系共重合体などを用いた砂型の長
所を兼ね備え、勝れた乾燥強度を有し、高品質・高精度
の鋳物の訪造に使用できる。In other words, the sand mold obtained by the present invention has the advantages of conventionally proposed sand molds using maleic anhydride copolymers, etc., has excellent dry strength, and is suitable for high-quality, high-precision castings. Can be used for visiting.
以下に本発明を更に詳しく説明する。The present invention will be explained in more detail below.
本発明は、1116以下のブタジェン/無水マレイン酸
共重合体の加水分解物のアルカリまたはアルカリ土類金
属塩の水溶液を、鋳物砂100重砥1に対して該加水分
解物の金属塩が0.1〜5重量部となるように鋳物砂と
註合し、成型後加熱乾燥して硬化せしめることを特徴と
した鋳物用砂型の製造法に関するものである。In the present invention, an aqueous solution of an alkali or alkaline earth metal salt of a hydrolyzate of a butadiene/maleic anhydride copolymer of 1116 or less is mixed with 0.0. The present invention relates to a method for manufacturing a foundry sand mold, characterized in that it is mixed with foundry sand in an amount of 1 to 5 parts by weight, and after molding, it is heated and dried to harden it.
本発明のブタジェン/無水マレイン酸共重合体は、無水
マレイン酸単位をほぼ50モル%右するものであって、
その製造は例えば、アセトン、メヂルエチルケトン、シ
クロヘキサノン、ヂオキサン、デメチルホルムアミド等
の極性溶媒、ベンビン等の非極性溶媒、またはこれらの
混合物等の溶媒中で、ブタジェンと無水マレイン酸とを
、過酸化ベンゾイル、アゾビスイソブチロニトリル等の
ラジカル重合開始剤を用いて、溶液重合、スラリー重合
などの方法により共重合さヒることにより行なわれる。The butadiene/maleic anhydride copolymer of the present invention contains approximately 50 mol% maleic anhydride units, and
Its manufacture is, for example, by combining butadiene and maleic anhydride in a polar solvent such as acetone, methyl ethyl ketone, cyclohexanone, dioxane, demethylformamide, a non-polar solvent such as benvin, or a mixture thereof. Copolymerization is carried out by a method such as solution polymerization or slurry polymerization using a radical polymerization initiator such as benzoyl oxide or azobisisobutyronitrile.
反応終了後溶媒を除去すれば共重合体が得られる。本発
明におけるブタジェン/無水マレイン酸の共重合体の分
子はは通常3,000〜300.000程度である。こ
の共重合体を水に溶解させると、!!I無水塁が開裂し
て、カルボキシル基となり加水分解物が得られる。実用
上は溶液重合の場合、反応溶媒の除去をスチームストリ
ッピングにより行なうと、溶媒の除去と同時に加水分解
物の水溶液が得られるので都合がよい。しかしながら、
加水分解物の水溶液を得るには、上述の方法により得た
共重合体を単離してあらためて水に溶解してもよい。こ
の水溶液にアルカリまたはアルカリ土類金属の酸化物ま
たは水酸化物などのアルjJり性を示す金属化合物、例
えば、水酸化ナトリウム、水酸化カリウム、水酸化マグ
ネシウム、酸化マグネシウム等を加えて中和すれば目的
とする水溶液が1uられる。ただしこのとき得られた水
溶液の1)11は6以下でなければならない。pHが6
より大きいと十分な乾燥強度が現われない。本発明のブ
タジェン/無水マレイン酸共重合体の加水分解物の金属
塩の水溶液は、その11!が5〜50%、好ましくは1
5〜40重量%であるものを使用するのが好ましい。5
重間%未満では硬化強度が不足し、また熱硬化に時間を
要するなどの理由で好ましくない。また、50E:Ql
1%を超える多聞の固形分では該水溶液が粘稠となりす
ぎて操作が困難になり、やはり好ましくない。After the reaction is completed, the solvent is removed to obtain a copolymer. The butadiene/maleic anhydride copolymer in the present invention usually has a molecular weight of about 3,000 to 300,000. When this copolymer is dissolved in water,! ! I anhydrous base is cleaved to become a carboxyl group and a hydrolyzate is obtained. Practically speaking, in the case of solution polymerization, it is convenient to remove the reaction solvent by steam stripping because an aqueous solution of the hydrolyzate can be obtained simultaneously with the removal of the solvent. however,
To obtain an aqueous solution of the hydrolyzate, the copolymer obtained by the above method may be isolated and redissolved in water. This aqueous solution is neutralized by adding metal compounds exhibiting alkaline properties such as alkali or alkaline earth metal oxides or hydroxides, such as sodium hydroxide, potassium hydroxide, magnesium hydroxide, and magnesium oxide. For example, 1 u of the desired aqueous solution is added. However, 1) 11 of the aqueous solution obtained at this time must be 6 or less. pH is 6
If it is larger, sufficient dry strength will not appear. The aqueous solution of the metal salt of the hydrolyzate of the butadiene/maleic anhydride copolymer of the present invention is No. 11! is 5 to 50%, preferably 1
Preferably, 5 to 40% by weight is used. 5
If the weight is less than % by weight, curing strength is insufficient and heat curing takes time, which is not preferable. Also, 50E:Ql
If the solid content exceeds 1%, the aqueous solution becomes too viscous and difficult to operate, which is also not preferred.
本発明の水溶液はその固形分が鋳物砂100咀♀部に対
して0.1〜5、好ましくは0.3〜3重聞部になる伍
を鋳物砂に添加湿練し、型に入れた後、加熱乾燥して硬
化せしめて鋳物用砂型を!li造する。The aqueous solution of the present invention has a solid content of 0.1 to 5 parts, preferably 0.3 to 3 parts per 100 parts of foundry sand, and is moistened with foundry sand and placed in a mold. After that, heat and dry to harden and create a foundry sand mold! li build.
0.1重石部より少ないと硬化強度が不足して好ましく
ない。If the amount is less than 0.1 part, the curing strength will be insufficient, which is not preferable.
また51吊部より多く使用しても特に硬化の増大は望め
ず、不経済となるだりである。Further, even if more than 51 hanging parts are used, no particular increase in hardening can be expected, which may be uneconomical.
本発明においては、鋳物砂と上記水溶液を混合後、型に
充填し硬化させる。成型俊、型に入れたまま、すなわら
脱型せずに、加熱乾燥することもできる。また加圧もし
くは圧縮成型後、脱型し、加熱乾燥してもよい。この場
合、湿態強度を向上°させる為に、従来公知の添加剤、
例えばでんぷん、しゅう酸、過ホウ素酸ナトリウムなど
を適宜の吊混合して用いることもできる。In the present invention, after mixing foundry sand and the aqueous solution, the mixture is filled into a mold and hardened. It is also possible to heat and dry the product while it is in the mold, without removing it from the mold. Further, after pressurization or compression molding, the mold may be removed and dried by heating. In this case, in order to improve the wet strength, conventionally known additives,
For example, starch, oxalic acid, sodium perborate, etc. may be appropriately mixed and used.
しかしながら本発明における鋳物砂と上記水溶液の混合
物は従来品に比べ流動性が良いので、手込め、あるいは
加圧振動、真空吸引圧などを利用した造型装置による成
型もできる。また、加熱操作は任意の方法で行なうこと
ができ、例えば真空加熱乾燥づる方法、加熱炉を利用す
る方法、温度50〜200℃、時間0.5〜10分の熱
風乾燥を利用する方法、あるいはマイクロ波加熱、誘電
加熱などを用いる方法などいずれの方法もとることがで
きる。特に熱風乾燥、マイクロ波加熱や誘電加熱による
加熱操作が、乾燥強度、硬化速度が良く好ましい。However, since the mixture of foundry sand and the above-mentioned aqueous solution in the present invention has better fluidity than conventional products, it can be molded by hand or by a molding device using pressurized vibration, vacuum suction pressure, etc. Further, the heating operation can be performed by any method, such as vacuum heating drying method, method using a heating furnace, method using hot air drying at a temperature of 50 to 200°C for 0.5 to 10 minutes, or Any method such as a method using microwave heating, dielectric heating, etc. can be used. In particular, heating operations using hot air drying, microwave heating, or dielectric heating are preferred because of their good dry strength and curing speed.
[発明の効果]
本発明によって得られる砂型は乾燥強度が大きく、高品
質、高精度の鋳物の鋳造に使用できる。[Effects of the Invention] The sand mold obtained by the present invention has high dry strength and can be used for casting high-quality, high-precision castings.
また有機バインダーの固形分としての使用量が少なくて
も十分な乾燥強度が得られるので経済的である。本発明
における有機バインダーの水溶液と鋳物砂との混合物は
、従来品に比べて流動性が良いので、容易でかつ十分な
型込めができる。すなわち、手込め、あるいは加圧lt
2勅、真空吸引圧などを利用した造型装置による成型も
できる。この場合、時に高圧力の加圧など必要がないの
で、木型など耐圧性の低い模型による成型でも複雑かつ
高精度の砂型ができる。Furthermore, sufficient dry strength can be obtained even if the amount of organic binder used as a solid content is small, so it is economical. The mixture of the organic binder aqueous solution and foundry sand in the present invention has better fluidity than conventional products, so it can be easily and sufficiently molded. In other words, manual or pressurized
Molding can also be performed using a molding device that uses vacuum suction pressure. In this case, there is no need for high pressure, so complex and highly accurate sand molds can be made even when molded using a model with low pressure resistance, such as a wooden mold.
本発明によって得られる砂型の残留強度(鋳造後)が適
当であるので、使用後(鋳造後)の砂型を破壊するのが
容易であるうえ、使用済みの砂の再使用ができる。Since the residual strength (after casting) of the sand mold obtained by the present invention is appropriate, it is easy to destroy the sand mold after use (after casting), and the used sand can be reused.
また、使用済みの砂による公害問題、例えば土壌汚染、
燃焼時の臭気の問題を起こずこともない。In addition, pollution problems caused by used sand, such as soil contamination,
It does not cause odor problems during combustion.
[実 施 例] 次に実施例により本発明を更に詳しく説明する。[Example] Next, the present invention will be explained in more detail with reference to Examples.
実施例 1
(バインダーの調製)
ラジカル触tIR(アゾビスイソブチロニトリル)によ
りアセトン中で、ブタジェンと無水マレイン酸を反応さ
せ、ブタジェン/無水マレイン酸共重合体のアセトン溶
液を得た。共重合体の分子量は約3万であり、また共重
合体中の無水マレイン酸単位の含有量は約50E−ル%
であった。Example 1 (Preparation of binder) Butadiene and maleic anhydride were reacted in acetone using radical catalytic tIR (azobisisobutyronitrile) to obtain an acetone solution of a butadiene/maleic anhydride copolymer. The molecular weight of the copolymer is approximately 30,000, and the content of maleic anhydride units in the copolymer is approximately 50E-le%.
Met.
次に、上記のアセトン溶液に、水蒸気を吹込み、アセト
ンを留去させるとともに共重合体中の酸無水基を開裂さ
せることによりブタジェン/無水マレイン酸共重合体の
加水分解物水溶液を得た。なお、IR分析などによると
、共重合体中の酸無水基は、はぼ全て開裂し、カルボキ
シル基になっていた。この水溶液に向性ソーダを加えて
カルボキシル基の一部を中和し、DH3,5の、ブタジ
ェン/無水マレイン酸共重合体の加水分解物のナトリウ
ム塩の水溶液を得た。Next, water vapor was blown into the above acetone solution to distill off the acetone and cleave the acid anhydride groups in the copolymer, thereby obtaining an aqueous solution of a hydrolyzate of a butadiene/maleic anhydride copolymer. According to IR analysis, almost all of the acid anhydride groups in the copolymer were cleaved to become carboxyl groups. A tropic soda was added to this aqueous solution to neutralize a portion of the carboxyl groups to obtain an aqueous solution of the sodium salt of a hydrolyzate of a butadiene/maleic anhydride copolymer with a DH of 3.5.
(バインダーの試験)
上記の如くして得られた加水分解物のナトリウム塩の水
溶液の濃度を、25重量%に調整して、次表に示す固形
分割合いでけい砂と混練した。この混合物は流動性があ
った。(Binder Test) The concentration of the aqueous solution of the sodium salt of the hydrolyzate obtained as described above was adjusted to 25% by weight, and the solution was kneaded with silica sand at the solid proportions shown in the following table. This mixture was fluid.
次に、SOWφX 50jlNの鋳型試験片作成用のを
に流し込んで充填、成型し、脱型せずに型ごと電子レン
ジ(0,5kw)で10分間加熱乾燥させた。加熱乾燥
後、試験片を取出し、乾燥強度を測定した。結果を次表
に示した。Next, a SOWφX 50 jlN mold for preparing a test piece was poured into a mold, filled and molded, and the mold was heated and dried in a microwave oven (0.5 kw) for 10 minutes without demolding. After heating and drying, the test piece was taken out and its dry strength was measured. The results are shown in the table below.
実施例1と同様にして得られたブタジェン/無水マレイ
ン酸共重合体の加水分解物水溶液に荷性ソーダを加えて
中和し、pH7,0とした。この水溶液で、実施例1と
同様にバインダーの試験を行なったところ、けい砂10
0Φ吊部に対して、固形分1.0重量部使用しても、試
験片の乾燥強度は0.5Kg/ cta稈度に過ぎなか
った。Loading soda was added to an aqueous solution of a hydrolyzate of a butadiene/maleic anhydride copolymer obtained in the same manner as in Example 1 to neutralize the solution to pH 7.0. Using this aqueous solution, a binder test was conducted in the same manner as in Example 1.
Even if 1.0 part by weight of solids was used for the 0Φ hanging part, the dry strength of the test piece was only 0.5 Kg/cta culm degree.
Claims (1)
水分解物のアルカリまたはアルカリ土類金属塩の水溶液
を、鋳物砂100重量部に対して該加水分解物の金属塩
が0.1〜5重量部となるように鋳物砂と混合し、成形
後加熱乾燥して硬化せしめることを特徴とする鋳物用砂
型の製造法。An aqueous solution of an alkali or alkaline earth metal salt of a hydrolyzate of a butadiene/maleic anhydride copolymer having a pH of 6 or less is mixed with 0.1 to 5 parts by weight of the metal salt of the hydrolyzate per 100 parts by weight of foundry sand. A method for producing a foundry sand mold, which comprises mixing the foundry sand with foundry sand so as to give the following properties, and heating and drying it after molding to harden it.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17524685A JPS6234645A (en) | 1985-08-09 | 1985-08-09 | Production of sand mold for casting |
| US06/888,010 US4691759A (en) | 1985-07-24 | 1986-07-22 | Binder for dry sand mold and method of its usage |
| EP86110222A EP0209906B1 (en) | 1985-07-24 | 1986-07-24 | Binder for dry sand mold and method of its usage |
| DE8686110222T DE3681763D1 (en) | 1985-07-24 | 1986-07-24 | BINDING AGENT FOR MOLDED SAND AND METHOD FOR ITS USE. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17524685A JPS6234645A (en) | 1985-08-09 | 1985-08-09 | Production of sand mold for casting |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS6234645A true JPS6234645A (en) | 1987-02-14 |
Family
ID=15992814
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17524685A Pending JPS6234645A (en) | 1985-07-24 | 1985-08-09 | Production of sand mold for casting |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6234645A (en) |
-
1985
- 1985-08-09 JP JP17524685A patent/JPS6234645A/en active Pending
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