JP3131790B2 - Green mold for casting and method for producing the same - Google Patents

Green mold for casting and method for producing the same

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Publication number
JP3131790B2
JP3131790B2 JP03183855A JP18385591A JP3131790B2 JP 3131790 B2 JP3131790 B2 JP 3131790B2 JP 03183855 A JP03183855 A JP 03183855A JP 18385591 A JP18385591 A JP 18385591A JP 3131790 B2 JP3131790 B2 JP 3131790B2
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JP
Japan
Prior art keywords
reduced
mold
casting
green
green 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.)
Expired - Lifetime
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JP03183855A
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Japanese (ja)
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JPH057976A (en
Inventor
要二郎 岩垣
和昭 加藤
Original Assignee
東和化成工業株式会社
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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、鋳物用生型及びその製
造方法に関する。
The present invention relates to a green mold for castings and a method for producing the same.

【0002】[0002]

【従来の技術】鋳物を製造する際に最も広汎に使用され
る鋳型としては、鋳物の外側を形成させる主型に多用さ
れる生型と、鋳物の空洞部分を形成させる中子に多用さ
れる自硬性鋳型がある。
2. Description of the Related Art Molds that are most widely used in the production of castings are often used in a green mold that is frequently used as a main mold for forming the outside of the casting and a core that is used to form a hollow portion of the casting. There is a self-hardening mold.

【0003】自硬性鋳型は、ケイ砂等の砂の他に粘結剤
としてセメントや水ガラス等の無機物、あるいは乾性
油、熱硬化性樹脂等の有機物が一般的に用いられるが、
特殊な方法として、特公昭51−46482号に紹介さ
れているように、ソルビトールと水溶性金属化合物及び
水を加えて硬化させる方法もある。
[0003] Self-hardening molds are generally made of inorganic substances such as cement and water glass, or organic substances such as drying oil and thermosetting resin, as binders, in addition to sand such as silica sand.
As a special method, there is a method in which sorbitol, a water-soluble metal compound and water are added and cured as introduced in JP-B-51-46482.

【0004】しかし、主型は特に高い硬度を要求されな
い場合が多く、硬度の高い自硬性砂型は使用前に硬化さ
せるための時間が長いことが作業上の支障になり、使用
後の粉砕等、再処理が必要になることもあって、安価な
ことと簡便なことの方が強く要求される主型には自硬性
鋳型があまり採用されず、より簡便な生型が多く採用さ
れている。
[0004] However, the main mold often does not require a particularly high hardness, and a self-hardening sand mold having a high hardness has a long working time for hardening before use, which hinders the work, and causes a problem such as grinding after use. Due to the need for reprocessing, self-hardening molds are rarely used for main molds that are more demanding for inexpensiveness and simplicity, and simpler green molds are often used.

【0005】生型は、自動車等に用いられる機械の鋳造
品を作る場合に用いられる最も簡便な主型で、一般的に
使用されている鋳型であり、古くは、粘土を含んだ山砂
に水を加えて使用されていたが、現在は、けい砂等の骨
材、粘土、水及び添加剤で構成されることが多い。
[0005] The green mold is the simplest main mold used for making a casting of a machine used for an automobile or the like, and is a commonly used mold. It was used with the addition of water, but at present it is often composed of aggregates such as silica sand, clay, water and additives.

【0006】主型として生型が広く使用されているの
は、生型が(1)造型した鋳型から直ちに模型を抜きと
り、中子を納め、上型と下型の型合わせを行って、その
まま注湯できること、(2)鋳物が比較的容易に取り出
せること、(3)崩された型砂は繰り返して使用するこ
とが可能で、且つ再生処理が簡単にできること、(4)
鋳型の材料費が安く、有毒ガス等の発生がないこと、な
どの利点を持っているためである。
[0006] A green mold is widely used as a main mold because (1) a green mold is immediately taken out of a molded mold, a core is put in, and an upper mold and a lower mold are matched. (2) The casting can be taken out relatively easily, (3) The broken mold sand can be used repeatedly, and the regeneration treatment can be easily performed, (4)
This is because the material cost of the mold is low and no toxic gas is generated.

【0007】[0007]

【発明が解決しようとする課題】しかし、従来の生型
は、前記のような利点を持ってはいるものの、一方で
は、(1)生型成形後の型及び内面が不安定であり、鋳物
の表面に凹凸が生じやすい、(2)乾燥時に生型の強度が
著しく低下しがちである、(3)注湯時に砂の巻き込みが
生じ易い、等の欠点があるので、それらの欠点を解消で
きるような、生型及びその製造方法の改善が期待されて
きた。
However, although the conventional green mold has the above advantages, on the other hand, (1) the mold and the inner surface after green molding are unstable, and (2) The strength of the green mold tends to be remarkably reduced during drying, (3) Sand is easily entangled during pouring, etc. It has been expected to improve the green mold and its manufacturing method as much as possible.

【0008】[0008]

【課題を解決するための手段】本発明者等は、前記諸々
の課題を解決するために、生型とその製造工程中の添加
剤及び得られる鋳物の関係を詳細に研究した。
Means for Solving the Problems In order to solve the above-mentioned various problems, the present inventors have studied in detail the relationship between a green mold, additives in a manufacturing process thereof and a casting obtained.

【0009】その結果、生型の製造工程中に、ある種の
糖アルコール、即ち、エリスリトール、ペンタエリスリ
トール、キシリトール、マンニトール、還元麦芽糖、還元
乳糖、還元澱粉加水分解物、還元キシロオリゴ糖から成
る群から選ばれる糖アルコールの一種又は二種以上の混
合物を添加して生型を製造することによって、鋳型の水
分が低く、かつコンパクタビリティが低いにも拘らず、
砂噛が起こりにくく、顕著に鋳肌の美しい鋳物を得るこ
とに成功し、本発明を完成するに至った。
As a result, during the green manufacturing process, certain sugar alcohols, namely erythritol, pentaerythritol, xylitol, mannitol, reduced maltose, reduced lactose, reduced starch hydrolysates, reduced xylo-oligosaccharides, By adding one or a mixture of two or more of the selected sugar alcohols to produce a green mold, the water content of the mold is low, and despite the low compactability,
The present invention succeeded in obtaining a casting in which sand biting hardly occurs and the casting surface was remarkably beautiful, and the present invention was completed.

【0010】即ち、本発明は第1に、エリスリトール、
ペンタエリスリトール、キシリトール、マンニトール、
還元麦芽糖、還元乳糖、還元澱粉加水分解物、還元キシ
ロオリゴ糖から成る群から選ばれる一種又は二種以上の
混合物を含有する、鋳物用生型である。
That is, the present invention firstly provides erythritol,
Pentaerythritol, xylitol, mannitol,
It is a raw casting mold containing one or a mixture of two or more selected from the group consisting of reduced maltose, reduced lactose, reduced starch hydrolyzate, and reduced xylo-oligosaccharide.

【0011】第2に、生型の製造工程中に、エリスリト
ール、ペンタエリスリトール、キシリトール、マンニト
ール、還元麦芽糖、還元乳糖、還元澱粉加水分解物、還
元キシロオリゴ糖から成る群から選ばれる一種又は二種
以上の混合物を添加して製造することを特徴とする、鋳
物用生型の製造方法である。
Secondly, one or more selected from the group consisting of erythritol, pentaerythritol, xylitol, mannitol, reduced maltose, reduced lactose, reduced starch hydrolyzate, and reduced xylo-oligosaccharide during the production process of the green mold. A method for producing a green mold for a casting, characterized by producing the mixture by adding a mixture of

【0012】第3に、生型の製造工程中に、エリスリト
ール、ペンタエリスリトール、キシリトール、マンニト
ール、還元麦芽糖、還元乳糖、還元澱粉加水分解物、還元
キシロオリゴ糖から成る群から選ばれる一種又は二種以
上の混合物を、0.1〜7.0重量%添加して製造するこ
とを特徴とする、鋳物用生型の製造方法である。
Third, one or more selected from the group consisting of erythritol, pentaerythritol, xylitol, mannitol, reduced maltose, reduced lactose, reduced starch hydrolyzate, and reduced xylo-oligosaccharide during the production process of the green mold. A mixture of 0.1 to 7.0% by weight to produce a green mold for casting.

【0013】第4に、生型の製造工程中に、エリスリト
ール、ペンタエリスリトール、キシリトール、マンニト
ール、還元麦芽糖、還元乳糖、還元澱粉加水分解物、還元
キシロオリゴ糖から成る群から選ばれる一種又は二種以
上の混合物を、0.1〜7.0重量%添加し、骨材、水、
並びに粘土を含有させて製造することを特徴とする、鋳
物用生型の製造方法である。
Fourth, one or more selected from the group consisting of erythritol, pentaerythritol, xylitol, mannitol, reduced maltose, reduced lactose, reduced starch hydrolyzate, and reduced xylo-oligosaccharide during the production process of the green mold. Was added in an amount of 0.1 to 7.0% by weight, and aggregate, water,
And a method for producing a green mold for casting, characterized by comprising a clay.

【0014】本発明に使用するエリスリトール、ペンタ
エリスリトール、キシリトール、マンニトール、還元麦
芽糖、還元乳糖、還元澱粉加水分解物、還元キシロオリ
ゴ糖から成る群から選ばれる一種又は二種以上の混合物
の原料由来は、特に制限する必要はなく、その純度等の
品質も、未還元物が多量に含まれていたり、ガスを発生
するような不純成分が含まれていたりしない限り、前記
の成分が主成分であれば、それ以上の詳細な制約を加え
る必要は無い。
The raw material of one or a mixture of two or more selected from the group consisting of erythritol, pentaerythritol, xylitol, mannitol, reduced maltose, reduced lactose, reduced starch hydrolyzate, reduced xylo-oligosaccharide used in the present invention is as follows: It is not particularly necessary to limit the quality, such as its purity, as long as the above components are the main components as long as the unreduced substances are contained in a large amount or an impurity component that generates gas is not contained. There is no need to add further detailed restrictions.

【0015】また、その状態も、水溶液、粉末、顆粒、
塊状のいずれでも用いることができるが、前記糖アルコ
ールを用いる場合には、比較的短い時間内にベントナイ
トや骨材等と均一に混合する必要がある等の理由から、
濃度70%前後の水溶液状であることが最も好ましい。
[0015] In addition, the state is, aqueous solution, powder, granules,
Any of the lumps can be used, but in the case of using the sugar alcohol, it is necessary to uniformly mix with the bentonite or aggregate within a relatively short time,
Most preferably, the aqueous solution has a concentration of about 70%.

【0016】本発明を実施する上で、エリスリトール、
ペンタエリスリトール、キシリトール、マンニトール、
還元麦芽糖、還元乳糖、還元澱粉加水分解物、還元キシ
ロオリゴ糖から成る群から選ばれる一種又は二種以上の
混合物は、本発明の効果を充分に発揮するためと云う理
由の他、安価であることや砂の再生が容易であること、
硫黄や窒素を含んだガスや有毒ガスの発生が無いこと等
の生型本来の特徴を失わないためにも、生型の重量に対
して0.1〜7重量%の範囲で添加することが好まし
い。
In practicing the present invention, erythritol,
Pentaerythritol, xylitol, mannitol,
One or a mixture of two or more selected from the group consisting of reduced maltose, reduced lactose, reduced starch hydrolyzate, and reduced xylo-oligosaccharides is inexpensive in addition to the reason that the effects of the present invention are sufficiently exhibited. The sand and sand are easy to regenerate,
In order not to lose the original characteristics of the raw type such as no gas containing sulfur or nitrogen or generation of toxic gas, it may be added in the range of 0.1 to 7% by weight based on the weight of the raw type. preferable.

【0017】この数値は特に臨界的なものではないが、
添加量が0.1重量%未満の場合には本発明の効果であ
る、砂噛み頻度の低下、表面安定性等が充分に得られな
いことが多くなるので好ましくなく、7重量%を超えて
添加した場合には、添加量の増大に効果の増大が伴わな
いことがあるので経済的に意味が薄く、更に、極端に添
加量が多い場合には、生型の湿態強度が使用に耐えない
程度まで低下することもあるので好ましくない。
Although this value is not particularly critical,
When the addition amount is less than 0.1% by weight, the effects of the present invention, such as a decrease in the frequency of sand biting and surface stability, are often not sufficiently obtained. When added, the increase in the amount of addition may not be accompanied by an increase in the effect, so it is economically insignificant. In addition, when the amount is extremely large, the wet strength of the raw type can withstand use. It is not preferred because it may be reduced to an unacceptable level.

【0018】また、本発明を実施するにあたって、使用
する他の鋳型成分の種類や量については特に通常の生型
製造時の範囲と異なった制約を設ける必要は無く、通常
の処方の例を挙げれば、前記添加剤を0.1〜7重量%
使用する場合には、砂100重量部前後、粘土7重量部
前後、水5重量部前後配合された素材が有利に使用され
る。
In practicing the present invention, there is no need to impose any restrictions on the types and amounts of other mold components used, which are different from the ranges used during normal green mold production. 0.1 to 7% by weight of the additive
When used, a material mixed with about 100 parts by weight of sand, about 7 parts by weight of clay, and about 5 parts by weight of water is advantageously used.

【0019】本発明には、山砂に限らず、川砂も海浜か
ら採取された砂も珪砂も使用可能であり、その砂は必ず
しも新砂でなくとも使用可能で、一度鋳型として使用後
再生した、いわゆる戻り砂であっても構わない。
In the present invention, not only mountain sand, but also river sand, sand collected from the beach, and quartz sand can be used, and the sand can be used even if it is not necessarily new sand. It may be so-called return sand.

【0020】また、本発明に使用する粘土としては、通
常の生型製造用粘土が全て採用可能であり、例えば、蛙
目粘土、木節粘土、ベントナイト、カオリン等がある。
As the clay used in the present invention, all ordinary clays for green mold production can be adopted, and examples thereof include frog-eye clay, kibushi clay, bentonite and kaolin.

【0021】更に、本発明を実施するに際して、従来か
ら使用されている各種添加剤、例えば、石炭粉、澱粉等
を使用することは任意に可能であり、本発明で使用する
添加剤との間に相乗的な効果を期待できる場合もある。
Further, in carrying out the present invention, it is arbitrarily possible to use various additives conventionally used, for example, coal powder, starch and the like. In some cases, a synergistic effect can be expected.

【0022】[0022]

【実施例】以下に実施例を掲げて本発明の内容を更に具
体的に説明するが、本発明は以下の実施例により制限さ
れるものではない。
EXAMPLES The content of the present invention will be described more specifically with reference to the following examples, but the present invention is not limited to the following examples.

【0023】[0023]

【実施例1】砂として鹿島産6号珪砂87.0重量部、
粘土としてベントナイト(ピロリン酸ソーダ法によるメ
チレンブルー吸着量が45〜50ml/0.5gのボルクレ
イ)6.5重量部、その他の添加剤として石炭粉[旭コ
ークス製、シーコール・15]2.5重量部及びα−澱粉
[日本食品化工(株)製、アルスター(B)]1.0重量部
が配合された素材を、2分間混練した。
Example 1 As a sand, 87.0 parts by weight of Kashima No. 6 silica sand,
6.5 parts by weight of bentonite (volclay having a methylene blue adsorption amount of 45 to 50 ml / 0.5 g by sodium pyrophosphate method) as a clay, 2.5 parts by weight of coal powder [Asahi Coke Co., Ltd., Seacol 15] as other additives and A raw material containing 1.0 part by weight of α-starch [manufactured by Nippon Shokuhin Kako Co., Ltd., Ulster (B)] was kneaded for 2 minutes.

【0024】そして、該素材に対し、水2.0重量部、
アマルティ[東和化成工業(株)製の還元麦芽糖の名称]
1.0重量部を添加し、これを発明区1としたのち、さ
らに15分間混練し、本発明品の生型を得た。
Then, 2.0 parts by weight of water,
Amalti [Name of reduced maltose manufactured by Towa Chemical Industry Co., Ltd.]
After adding 1.0 part by weight and setting this as Invention Zone 1, kneading was further performed for 15 minutes to obtain a green mold of the product of the present invention.

【0025】また、上記素材に対し、水2.0重量部、
PO−40[東和化成工業(株)製の還元澱粉加水分解
物]1.0重量部を添加し、これを発明区2としたの
ち、さらに15分間混練し、成形して本発明品の生型を
得た。
In addition, 2.0 parts by weight of water,
1.0 part by weight of PO-40 [reduced starch hydrolyzate manufactured by Towa Kasei Kogyo Co., Ltd.] was added thereto, and this was designated as Invention Zone 2. Then, the mixture was kneaded for another 15 minutes, molded and molded to obtain the product of the present invention. I got the mold.

【0026】なお、上記素材に対し、水2.5重量部を
用いたものを対照区1とし、各発明区と同様に、さら
に、15分間混練し、成形して対照品の生型を得た。
The above-mentioned material was used as a control group 1 using 2.5 parts by weight of water, and kneaded and molded for 15 minutes in the same manner as in each invention section to obtain a green mold of a control product. Was.

【0027】発明区1、発明区2、対照区1の配合割合
を表1に示す。
Table 1 shows the proportions of Invention Section 1, Invention Section 2 and Control Section 1.

【0028】[0028]

【表1】 [Table 1]

【0029】上記で得た三通りの生型と同様の成形前混
練品を、JIS−Z2603に規定する試験片つき固め
機(内径50mm、長さ150mmの円筒形枠)を用い
て、各区について8個の生型試験片をそれぞれ調製し
た。
The same kneaded product before molding as the three types of green molds obtained above was used for each section using a compacting machine with a test piece (a cylindrical frame having an inner diameter of 50 mm and a length of 150 mm) specified in JIS-Z2603. Eight raw test pieces were prepared.

【0030】発明区1、発明区2、対照区1について、
成形前混練品を用いて、JIS−Z2605にて水分
を、JIS−Z2604にて抗圧力を測定し、生型試験
片を用いて日本鋳物協会東海支部試験方法により表面安
定度及びコンパクタビリティーを、それぞれ測定した。
For Invention Zone 1, Invention Zone 2, and Control Zone 1,
Using the kneaded product before molding, the water content was measured according to JIS-Z2605, and the coercive pressure was measured according to JIS-Z2604. The surface stability and compactability were determined using the green casting test pieces according to the Japan Casting Association Tokai Branch Test Method. , Respectively.

【0031】なお、測定に当たっては、型成形直前の各
条件の混練品についての水分及びコンパクタビリテイ−
を測定した。
In the measurement, the water content and compactability of the kneaded product under each condition immediately before molding were determined.
Was measured.

【0032】また、抗圧力及び表面安定度については、
成形直後、成形後1時間、成形後3時間、成形後24時
間に、それぞれ測定した。
Further, regarding the coercive pressure and the surface stability,
The measurement was performed immediately after molding, 1 hour after molding, 3 hours after molding, and 24 hours after molding.

【0033】そして、成形直前の水分とコンパクタビリ
ティーの測定結果を表2に、成形後の経過時間と抗圧力
及び表面安定度を表3に、それぞれ示す。
Table 2 shows the measurement results of water content and compactability immediately before molding, and Table 3 shows the elapsed time, coercive pressure and surface stability after molding.

【0034】なお、表3中、抗圧力の単位はkg/cm2
表面安定度は%で表わした。
In Table 3, the unit of the coercive pressure is kg / cm 2 ,
The surface stability was expressed in%.

【0035】[0035]

【表2】 [Table 2]

【0036】[0036]

【表3】 [Table 3]

【0037】表2、表3から、還元麦芽糖又は還元澱粉
加水分解物を添加した本発明区の生型は、成形後の抗圧
力、表面安定度が共に対照区の生型よりも優れているこ
とが明らかである。
Tables 2 and 3 show that the green mold of the present invention to which the reduced maltose or the reduced starch hydrolyzate was added was superior to the green mold of the control group in both the pressure resistance and the surface stability after molding. It is clear that.

【0038】[0038]

【実施例2】砂として三河産6号珪砂200重量部、粘
度としてベントナイト(ピロリン酸ソーダ法によるメチ
レンブルー吸着量が45〜50ml/0.5gのボルクレイ)
14重量部が配合された素材を、2分間混練した。
Example 2 200 parts by weight of Mikawa No. 6 silica sand as sand and bentonite as viscosity (Volclay with methylene blue adsorption of 45 to 50 ml / 0.5 g by sodium pyrophosphate method)
The material containing 14 parts by weight was kneaded for 2 minutes.

【0039】そして、該素材に対し、表4に示すように
水とアマルティ[東和化成工業(株)製の還元麦芽糖の名
称]液との割合を変えて添加して発明区3〜発明区6と
し、また表5に示すように水とミルヘン[東和化成工業
(株)製の還元乳糖の名称]液との割合を変えて添加して
発明区7〜発明区10とし、更に表6に示すように水とエ
リスリトールとの割合を変えて添加して発明区11〜発明
区14としたのち、それぞれの発明区を、さらに15分間
混練し、成形して本発明品の生型を、それぞれ得た。
Then, as shown in Table 4, the ratio of water and Amalti (name of reduced maltose manufactured by Towa Kasei Kogyo Co., Ltd.) solution was changed to the raw material and added to the material, and the invention zone 3 to the invention zone 6 were added. And as shown in Table 5, water and mil hen [Towa Chemical Industry
[Name of reduced lactose manufactured by Co., Ltd.] The ratio of the solution to the invention was changed to be added to make invention zone 7 to invention zone 10, and as shown in Table 6, the ratio of water and erythritol was changed to add the invention zone. After setting the invention section to the invention section 14, each invention section was further kneaded for 15 minutes and molded to obtain a green mold of the product of the present invention.

【0040】なお、各糖アルコールは全て70%水溶液
にして用いた。
Each of the sugar alcohols was used as a 70% aqueous solution.

【0041】また、上記素材に対し、水3.3重量部を
用いたものを対照区2とし、各発明区と同様に、さら
に、15分間混練し、成形して対照品の生型を得た。
Further, the above-mentioned material, which was obtained by using 3.3 parts by weight of water, was used as a control group 2 and kneaded and molded for 15 minutes in the same manner as in each invention section to obtain a green mold of a control product. Was.

【0042】[0042]

【表4】 [Table 4]

【0043】[0043]

【表5】 [Table 5]

【0044】[0044]

【表6】 [Table 6]

【0045】上記で得た各区の生型と同様の成形前混練
品を、JIS−Z2603に規定する試験片つき固め機
(内径50mm、長さ150mmの円筒形枠)を用い、
各区について11個の生型試験片をそれぞれ調製した。
The same kneaded product before molding as the green mold of each section obtained above was compacted using a compacting machine with a test piece (a cylindrical frame having an inner diameter of 50 mm and a length of 150 mm) specified in JIS-Z2603.
Eleven raw test pieces were prepared for each section.

【0046】各区について、成形前混練品を用いて水分
及びコンパクタビリティーを測定し、その他の項目は、
成形後の試験片を用いて測定したが、その方法は、JI
S−Z2605にて水分を、JIS−Z2604にて湿
態強度を、日本鋳物協会東海支部試験方法により表面安
定度及びコンパクタビリティーを、JIS−Z2603
にて通気度を、日本鋳物協会東海支部試験方法により充
填密度を、また、丹治法により爆熱亀裂発生時間をそれ
ぞれ測定した。
For each section, the moisture and compactability were measured using the kneaded product before molding.
The measurement was performed using a test piece after molding.
S-Z2605: moisture, JIS-Z2604: wet strength, Japan Foundry Association Tokai Branch test method: surface stability and compactability, JIS-Z2603
, The packing density was measured by the Japan Casting Association Tokai Branch Test Method, and the explosion heat crack initiation time was measured by the Tanji Method.

【0047】なお、測定に当たっては、型成形直前に各
条件の混練品についての水分及びコンパクタビリテイ−
を測定した。
In the measurement, the water content and compactability of the kneaded product under each condition were measured immediately before the molding.
Was measured.

【0048】また、抗圧力及び表面安定度については、
成形直後、成形後1時間、成形後3時間、成形後24時
間に、それぞれ測定した。
As for the coercive pressure and the surface stability,
The measurement was performed immediately after molding, 1 hour after molding, 3 hours after molding, and 24 hours after molding.

【0049】そして、アマルティ液を添加した発明区
(発明区3〜発明区6)の測定結果を表7に、ミルヘン
液を添加した発明区(発明区7〜発明区10)の測定結果
を表8に、エリスリトールを添加した発明区(発明区11
〜発明区14)の測定結果を表9に、対照区2の測定を結
果を表10にそれぞれ示す。
Table 7 shows the measurement results of the invention sections to which the Amalti solution was added (invention section 3 to invention section 6), and the measurement results of the invention section to which the milchen solution was added (invention section 7 to invention section 10). 8, the invention zone to which erythritol was added (invention zone 11
Table 9 shows the measurement results of the invention group 14), and Table 10 shows the measurement results of the control group 2).

【0050】[0050]

【表7】 [Table 7]

【0051】[0051]

【表8】 [Table 8]

【0052】[0052]

【表9】 [Table 9]

【0053】[0053]

【表10】 [Table 10]

【0054】表7〜表10から、還元麦芽糖、還元乳糖
又はエリスリトールを使用した発明区の生型は、コンパ
クタビリティーが極端に大きく成らないにも拘らず、通
気度が比較的に高く、成形後の湿態強度、表面安定度、
爆熱亀裂発生時間について、対照区2に較べ優れている
ことが明らかになっている。
From Tables 7 to 10, it can be seen that the green mold of the invention using reduced maltose, reduced lactose or erythritol has a relatively high air permeability, despite the fact that the compactability does not become extremely large. After wet strength, surface stability,
It is clear that the explosion heat crack initiation time is superior to that of the control section 2.

【0055】[0055]

【発明の効果】本発明によると、生型成形後の型及び内
面が安定しているので、鋳物の表面に凹凸が生じ難く、
また、乾燥時に生型の強度が著しく低下せず、注湯時に
砂の巻き込みが生じ難い。
According to the present invention, since the mold and the inner surface after green molding are stable, irregularities are hardly generated on the surface of the casting.
In addition, the strength of the green mold is not significantly reduced during drying, and sand is hardly caught during pouring.

───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) B22C 1/00 - 3/00 ──────────────────────────────────────────────────続 き Continuation of front page (58) Field surveyed (Int. Cl. 7 , DB name) B22C 1/00-3/00

Claims (4)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 エリスリトール、ペンタエリスリトー
ル、キシリトール、マンニトール、還元麦芽糖、還元乳
糖、還元澱粉加水分解物、還元キシロオリゴ糖から成る
群から選ばれる一種又は二種以上の混合物を含有する、
鋳物用生型。
1. A composition comprising one or a mixture of two or more selected from the group consisting of erythritol, pentaerythritol, xylitol, mannitol, reduced maltose, reduced lactose, reduced starch hydrolyzate, and reduced xylo-oligosaccharide.
Raw mold for casting.
【請求項2】 生型の製造工程中に、エリスリトール、
ペンタエリスリトール、キシリトール、マンニトール、
還元麦芽糖、還元乳糖、還元澱粉加水分解物、還元キシ
ロオリゴ糖から成る群から選ばれる一種又は二種以上の
混合物を添加して製造することを特徴とする、鋳物用生
型の製造方法。
2. An erythritol,
Pentaerythritol, xylitol, mannitol,
A method for producing a green mold for casting, characterized by adding one or a mixture of two or more selected from the group consisting of reduced maltose, reduced lactose, reduced starch hydrolyzate, and reduced xylo-oligosaccharide.
【請求項3】 生型の製造工程中に、エリスリトール、
ペンタエリスリトール、キシリトール、マンニトール、
還元麦芽糖、還元乳糖、還元澱粉加水分解物、還元キシロ
オリゴ糖から成る群から選ばれる一種又は二種以上の混
合物を、生型の重量に対して0.1〜7.0重量%添加し
て製造することを特徴とする、鋳物用生型の製造方法。
3. An erythritol,
Pentaerythritol, xylitol, mannitol,
One or more mixtures selected from the group consisting of reduced maltose, reduced lactose, reduced starch hydrolysates, and reduced xylo-oligosaccharides are added in an amount of 0.1 to 7.0% by weight based on the weight of the raw mold. A method for producing a green mold for castings.
【請求項4】 生型の製造工程中に、エリスリトール、
ペンタエリスリトール、キシリトール、マンニトール、
還元麦芽糖、還元乳糖、還元澱粉加水分解物、還元キシロ
オリゴ糖から成る群から選ばれる一種又は二種以上の混
合物を、生型の重量に対して0.1〜7.0重量%添加し、
骨材、水、並びに粘土を含有させて製造することを特徴
とする、鋳物用生型の製造方法。
4. An erythritol,
Pentaerythritol, xylitol, mannitol,
One or more mixtures selected from the group consisting of reduced maltose, reduced lactose, reduced starch hydrolyzate, and reduced xylo-oligosaccharides are added in an amount of 0.1 to 7.0% by weight based on the weight of the raw mold ,
A method for producing a green mold for casting, characterized by comprising an aggregate, water and clay.
JP03183855A 1991-06-28 1991-06-28 Green mold for casting and method for producing the same Expired - Lifetime JP3131790B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP03183855A JP3131790B2 (en) 1991-06-28 1991-06-28 Green mold for casting and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP03183855A JP3131790B2 (en) 1991-06-28 1991-06-28 Green mold for casting and method for producing the same

Publications (2)

Publication Number Publication Date
JPH057976A JPH057976A (en) 1993-01-19
JP3131790B2 true JP3131790B2 (en) 2001-02-05

Family

ID=16143005

Family Applications (1)

Application Number Title Priority Date Filing Date
JP03183855A Expired - Lifetime JP3131790B2 (en) 1991-06-28 1991-06-28 Green mold for casting and method for producing the same

Country Status (1)

Country Link
JP (1) JP3131790B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014018851A (en) * 2012-07-23 2014-02-03 Asahi Tec Corp Method of producing core and core

Also Published As

Publication number Publication date
JPH057976A (en) 1993-01-19

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