JPS5844944A - Casting sand - Google Patents

Casting sand

Info

Publication number
JPS5844944A
JPS5844944A JP14250281A JP14250281A JPS5844944A JP S5844944 A JPS5844944 A JP S5844944A JP 14250281 A JP14250281 A JP 14250281A JP 14250281 A JP14250281 A JP 14250281A JP S5844944 A JPS5844944 A JP S5844944A
Authority
JP
Japan
Prior art keywords
sand
water glass
aggregate
casting
foundry
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
Application number
JP14250281A
Other languages
Japanese (ja)
Inventor
Koji Matsuoka
宏治 松岡
Toshio Kai
貝 敏雄
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.)
Mitsubishi Heavy Industries Ltd
Original Assignee
Mitsubishi Heavy Industries 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 Mitsubishi Heavy Industries Ltd filed Critical Mitsubishi Heavy Industries Ltd
Priority to JP14250281A priority Critical patent/JPS5844944A/en
Publication of JPS5844944A publication Critical patent/JPS5844944A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22CFOUNDRY MOULDING
    • B22C1/00Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
    • B22C1/16Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents
    • B22C1/167Mixtures of inorganic and organic binding agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Inorganic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Mold Materials And Core Materials (AREA)

Abstract

PURPOSE:To decrease residual compressive strength and burning by coating water glass on the surfaces of refractory aggregate or adding an org. binder to old sand of water glass base and mixing both materials. CONSTITUTION:Molding sand prepd. by coating water glass on the surfaces of refractory aggregate (silica sand, zircon sand, chromite sand) or using old sand of water glass base as aggregate, adding an org. binder (phenolic resin, alkyd resin) which cures even with alkalinity to said sand and mixing both materials. Such molding sand has low residual compressive strength and causes less burning, thus preventing casting defects such as high temp. cracking of castings.

Description

【発明の詳細な説明】 本発明は、従来の水ガラスを粘結材とする鋳物砂と、7
ラン樹脂のような有機系粘結材を用いた鋳物砂の長所t
そのまま残し、しかもそれぞれの欠点を解消した鋳物砂
に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides foundry sand using conventional water glass as a caking agent, and 7
Advantages of foundry sand using organic binder such as orchid resin
This relates to foundry sand that remains as it is and eliminates its respective drawbacks.

鋳鋼や大物鋳鉄用鋳型は、骨材(耐火材)として珪砂、
ジルコン砂、クロマイト砂等が使用され、粘結材として
は水ガラスが多用されて−るが、最近は7ラン樹脂を使
用することが増加して−る。
Cast steel and large cast iron molds use silica sand as aggregate (refractory material).
Zircon sand, chromite sand, etc. are used, and water glass is often used as a caking agent, but recently 7-run resin has been increasingly used.

これらの粘結材を使用した鋳型は、次のような欠点があ
る。
Molds using these binders have the following drawbacks.

(1)水ガラスを粘結材とする鋳物砂は、流動性が悪く
(粘性が高く)、鋳mt−造溢する時間が多くなる。
(1) Foundry sand using water glass as a caking agent has poor fluidity (high viscosity) and takes a long time to overflow during casting.

(2)  水ガラスを粘結材とする鋳物砂で造型された
鋳型は、鋳込時の熱で水ガラスと骨材が焼結し、鋳型の
崩壊性が悪くなp鋳物の砂落し工数が増加する。
(2) Molds made with foundry sand that uses water glass as a caking agent are sintered by the water glass and aggregate due to the heat during casting, resulting in poor mold disintegration and reducing the number of sand removal steps required for P castings. To increase.

(3)  水ガラスを粘結材とする鋳型から回収された
古?(水ガラス系古砂)Fi、再生処理が困難なため、
再度使用する場合、骨材表面に残留する水lラスと新た
に添加された水ガラスによって耐火性が低下し、中子や
肌砂としては使用できなめ。
(3) Ancient material recovered from molds using water glass as a binding agent? (Water glass old sand) Fi, because it is difficult to recycle,
When used again, the fire resistance decreases due to the water glass remaining on the surface of the aggregate and the newly added water glass, making it impossible to use it as core or skin sand.

(4)7ラン樹脂を粘結材とする鋳物砂は、熱膨談が大
きく、tた高温域で可縮性(クッション性)がtk%A
ため、ペーニング、鋳着、鋳物の高温割れ等の鋳造欠陥
が生じる。
(4) Foundry sand that uses 7-run resin as a caking agent has a large thermal expansion, and its compressibility (cushioning properties) in the high temperature range is tk%A.
As a result, casting defects such as paning, adhesion, and hot cracking of the casting occur.

一方、上記鋳物?(鋳11)には、次のような長所があ
る。
On the other hand, the above casting? (Cast 11) has the following advantages.

(1)  水ガラスを粘結材とする鋳物砂は、高温域で
可縮性(可撓性)があり、ベーニングや高温割れのよう
な鋳造欠陥が少ない。
(1) Foundry sand that uses water glass as a caking agent is compressible (flexible) in a high temperature range and has few casting defects such as veining and hot cracking.

(2)  フラン樹脂を粘結材とする鋳物砂は、流動性
が良好であり、造型時間が少ない。
(2) Foundry sand using furan resin as a caking agent has good fluidity and requires less molding time.

(3)7ラン樹脂を粘結材とする鋳型は、崩壊性が良好
でToシ、鋳物の砂落し工数が少な10(4)7ラン樹
脂を粘結材とする鋳物砂は、回収裏生処理が容易であ夛
、鋳物砂が繰返し使用できる。
(3) Molds using 7-run resin as a binder have good collapsibility and require less man-hours for removing sand from castings. It is easy to process and the foundry sand can be used repeatedly.

以上のように、鋳鋼や大物鋳鉄用鋳型の粘結材は、鋳物
砂の造型性、古砂の再使用の容易さの点から、水ガラス
よりフラン樹脂へ徐々に移行しつつある。しかし、7ラ
ン樹脂を粘結材とした鋳物砂は、高温斌で可縮性がなく
、骨材の膨張が直接鋳物に作用するため、鋳型の膨張に
よるベーニング、ベーニングに起因する燐層、あるiは
鋳物の凝固収縮が鋳型の膨張によって拘束される結果と
して生じる高温割れ等の鋳造欠陥が、水ガラスを粘結材
とするものよりも多く発生している。
As described above, the binder for molds for cast steel and large cast iron is gradually shifting from water glass to furan resin due to the moldability of foundry sand and the ease of reusing old sand. However, molding sand using 7-run resin as a binder is not compressible at high temperatures, and the expansion of the aggregate acts directly on the casting. In the case of i, casting defects such as hot cracking caused by the solidification shrinkage of the casting being restricted by the expansion of the mold occur more frequently than in those using water glass as the caking agent.

とのような問題を解決するために多くの試みが1にされ
ておシ、例えば、 (1)  粘結材添加量を極力少くして鋳型の高温強度
を低下させる方法、 (2)  木粉中ポリスチレン勢ポリマの粉末を添加し
、鋳込時の熱で消失畜せて鋳型に可縮性を付与する方法
、 (3)鋳着O発・生じ易%/%部分に不純物の多i低級
骨材を使用して骨材の軟化、溶融による可縮性會付与す
る方法、 等がある。
Many attempts have been made to solve these problems, such as: (1) reducing the high-temperature strength of the mold by minimizing the amount of binder added; (2) wood flour. A method of adding medium polystyrene-based polymer powder and making it disappear in the heat during casting to give the mold flexibility. There are methods such as using aggregate to soften and melt the aggregate to make it compressible.

しかし、このような方法にも、 (1)の場合は、常温強度の点で添加量の減少に1限R
があシ、 (2)の場合は、粉末の増加により粘結材の添加量t%
増加させなければならず、 (3)の場合は、再生による繰返し使用により低級砂が
蓄積し、全体の耐火性が低下する、郷の問題がある。
However, even with this method, in the case of (1), there is a limit of R for reducing the addition amount in terms of room temperature strength.
In the case of (2), the amount of caking agent added is t% due to the increase in powder.
In the case of (3), there is a problem in that low-grade sand accumulates due to repeated use through recycling, reducing the overall fire resistance.

従って、現在抹、ペーニングおよび鋳着防止対策として
、膨張の小さいクロマイト砂あるiはジルコン砂が鋳型
の一@I/C使用されているが、砂のコストが高−こと
、および再生砂中に蓄積した場合の影響が不明である仁
とが問題である。
Therefore, currently, chromite sand with low expansion and zircon sand are used as a measure to prevent molding, paning, and adhesion.However, the cost of sand is high, and recycled sand is The problem is that the effects of accumulation are unknown.

本発明は、以上の諸点に鑑み、有機系粘結材特有の鋳物
砂の流動性と鋳型の崩壊性および再生処理のし易さを残
しながら、水ガラス6高温域での可縮、性を利用して、
前記のフラン砂に見られるペーニング、燐層、鋳物の高
温割れのな一鋳物砂會提供するものである。
In view of the above points, the present invention has been developed to improve the shrinkability and properties of water glass 6 at high temperatures while maintaining the fluidity of foundry sand, the collapsibility of molds, and the ease of recycling that are unique to organic binders. Take advantage of
The present invention provides a foundry sand that eliminates the panning, phosphorus layer, and hot cracking of castings found in the above-mentioned Fran sand.

す表わち本発明は、珪砂、クロマイト砂、ジルーン砂等
の耐火性骨材の表面に可縮性付与のタメに水ガラスを着
接してコーティングナンドとし、該コーティングサンド
または水ガラス系古砂を骨材としてアルカリ中でも硬化
する有機系粘結材を添加混練した鋳物砂に関するもので
ある。
In other words, the present invention provides coating sand by adhering water glass to the surface of refractory aggregate such as silica sand, chromite sand, and Jirune sand to impart shrinkability, and coating sand or water glass-based old sand. The present invention relates to foundry sand made by adding and kneading an organic binder that hardens even in alkali as an aggregate.

本発明鋳物砂は、先ず、上記の通常の耐火性骨材に水ガ
ラスを添加混合してコーティングサンドとするのである
が、この場合の水jラスの添加量は、1重量%未満であ
ると本発明で目的とする鋳型の可縮性が得られず、また
10重量it越えると鋳型の耐火度が低下し、燐層等の
鋳型欠陥が発生するので、1〜10重量%とするのが好
ましい。
The foundry sand of the present invention is made by first adding and mixing water glass to the above-mentioned ordinary fire-resistant aggregate to form a coating sand. In this case, the amount of water glass added is less than 1% by weight. The desired mold shrinkability of the present invention cannot be obtained, and if the weight exceeds 10 weight it, the fire resistance of the mold decreases and mold defects such as a phosphorus layer occur, so it is recommended to set the amount to 1 to 10 weight %. preferable.

なお、本発’lにjIP−では、上記のコーティングサ
ンドの代プに、水ガラス系の古砂を用−ることもてきる
In addition, in the present invention, water glass-based old sand can be used as a substitute for the above-mentioned coating sand.

次iで、上記Oコーティングサンドtたは水ガラス系古
砂(以下、;−ティングサンドと称す)K添加搗練する
有機系粘結材としては、通常のフェノール樹脂、アルキ
ッド樹脂等のように水ガラスのアルカリ中でも硬化し得
るものが使用でき、そO添加量は砂の性状(粒度分布、
粒形% P1’%温度、比重尋)や気温勢によって変化
するが、余シ少な過ぎても鋳’INK必要な強度が得ら
れず、tた余り多過ぎても過剰強度となって各種のガラ
ス欠陥が発°生ずるため、通常はO,S〜2.0重量−
とするのが好ましい。
In the next step, the above-mentioned O-coating sand or old water glass sand (hereinafter referred to as ;-ting sand) can be used as the organic binder to be mixed with K, such as ordinary phenolic resin, alkyd resin, etc. Water glass that can be hardened even in alkali can be used, and the amount of O added depends on the properties of the sand (particle size distribution,
Particle shape % P1'% (temperature, specific gravity) and temperature change, but if there is too little, the required strength of the casting will not be obtained, and if there is too much, it will result in excessive strength and various types of Because glass defects occur, it is usually O,S~2.0wt.
It is preferable that

また、本発明鋳物砂にお−では、通常の硬化材、促進材
t−着干量添加混合することもできる。
In addition, the foundry sand of the present invention may be mixed with ordinary hardening agents and accelerators in dry amounts.

以下、実施例t−あげて本発明鋳物砂の作用、効果を具
体的に説明する。
Hereinafter, the functions and effects of the foundry sand of the present invention will be specifically explained using Example t.

実施例 1 上記配合のうち、先ず、珪砂と水ガラス會混練した後1
05±5℃で乾燥して水ガラス;−ティング砂とし、こ
の砂に対してフェノール樹脂組成物を混練し、更にポリ
イソシアネート組成物とピリジン誘導体組成°゛−の混
合物を添加混合した。得られた鋳物砂を鋳物砂1とする
Example 1 Among the above formulations, first, after kneading silica sand and water glass, 1
The sand was dried at 05.+-.5.degree. C. to obtain water glass sand, a phenol resin composition was kneaded into the sand, and a mixture of a polyisocyanate composition and a pyridine derivative composition was added and mixed. The obtained foundry sand is referred to as foundry sand 1.

実施例 2 上記配合の混線方法は、実施例1と同様とした。得られ
た鋳物−を鋳物Tip2とする。
Example 2 The cross-wire method for the above formulation was the same as in Example 1. The obtained casting is referred to as casting Tip 2.

以上の鋳物砂1,2のはかに、比較のために珪砂(新砂
)t−骨材とし水ガラスを粘結材とする鋳物砂(比較#
!1とする)と、珪砂(新砂)を骨材とし7ラン樹脂會
粘結材とする鋳物砂(比較妙2とする)tIII製した
。これら鋳物砂1.2と比較砂1,2と管用いて11×
2インチのI11試験片(鋳m>と50φ版5ON−の
第2試験片(鋳m)’を調製し、膨張特性と崩壊性を調
べた。
In addition to the above foundry sands 1 and 2, for comparison, foundry sand with silica sand (new sand) T-aggregate and water glass as caking agent (comparison #
! 1) and foundry sand (comparatively designated 2) using silica sand (new sand) as an aggregate and a 7-run resin caking agent. Using these foundry sand 1.2 and comparative sand 1,2 and pipe 11×
A 2-inch I11 test piece (cast m>) and a second test piece (cast m)' of a 50φ plate 5ON- were prepared, and the expansion characteristics and collapsibility were examined.

(1)膨張特性: 上記lit試験片會1150℃の炉中(舅鵞雰囲気)へ
挿入し、急熱膨張の経時変化音測定した。結果は、第1
図に示す通シであった。
(1) Expansion characteristics: The above lit test piece was inserted into a furnace at 1150° C. (inner atmosphere), and the sound of rapid thermal expansion over time was measured. The result is the first
It was the same as shown in the figure.

蚊図中、1は比較砂1の、2は比較砂2の、5は本発明
による鋳物#1の測定結果を示す。
In the mosquito diagram, 1 indicates the measurement results of comparative sand 1, 2 indicates the measurement results of comparative sand 2, and 5 indicates the measurement results of casting #1 according to the present invention.

なお、本発明による鋳物砂2も鋳物砂1とほぼ同様の結
果が得られてiる。
It should be noted that almost the same results as foundry sand 1 were obtained with foundry sand 2 according to the present invention.

第1図から明らかなように、水ガラスを粘結材とする比
較砂1の場合、加熱初期には骨材の膨張虻よって鋳型が
膨張するが、水ガラスが軟化すると鋳型が収縮する。従
って、比較砂1による鋳型を用−て鋳造する場合は、水
ガラス軟化時の鋳型の収縮が鋳型の部分的な膨張や鋳物
の凝固収縮を吸収して、ペーニンダ、高温割れ等の鋳造
欠陥を防止するのである。
As is clear from FIG. 1, in the case of comparative sand 1 using water glass as a caking agent, the mold expands due to the expansion of the aggregate at the initial stage of heating, but when the water glass softens, the mold contracts. Therefore, when casting using a mold made of Comparative Sand 1, the shrinkage of the mold during the softening of water glass absorbs the partial expansion of the mold and the solidification shrinkage of the casting, thereby preventing casting defects such as peninda and hot cracking. It is to prevent it.

これに対し、7ラン樹脂を粘結材とする比職砂2の場合
、811図から明らかなように、加熱初期は比較砂1と
同様に膨張するが、その後も緩やかではあるが膨張を続
ける。従って、比較砂2による鋳mを用めて鋳造する場
合は、鋳型の割れ→ベーニング、溶融金属の侵透、ある
いは鋳物の凝固収縮を拘束して高温割れが発生するので
ある。
On the other hand, in the case of Hishoku Sand 2, which uses 7-run resin as a binder, as is clear from Figure 811, it expands in the same way as Comparative Sand 1 at the initial stage of heating, but continues to expand after that, albeit slowly. . Therefore, when casting is performed using the casting m made of Comparative Sand 2, hot cracking occurs due to cracking of the mold → vening, penetration of molten metal, or restraint of solidification shrinkage of the casting.

一方、本発明による鋳物砂1の場合、纂1図から明らか
なように、比較砂1と同様の膨張、収縮の傾向を示す。
On the other hand, in the case of the foundry sand 1 according to the present invention, as is clear from Fig. 1, it exhibits the same tendency of expansion and contraction as the comparative sand 1.

これは45図(6)(常温の状態)、@(加熱後゛の状
態)K模式的に示すように、加熱によって骨材150表
肉に被覆した水ガラス12が軟化し、骨材1sの膨張を
吸収することによるものである。従って、本発明による
鋳物砂を用いた鋳型での鋳造の場合、水ガラスを粘結材
とする比較砂1と同様に高温割れ勢の鋳造欠陥が発生し
ないOである。なお、第3図(4)中の11は有機系粘
結材を、!51E103)中の11′はその炭化物を示
す。
As shown schematically in Figure 45 (6) (state at room temperature) @ (state after heating), the water glass 12 coated on the surface of the aggregate 150 is softened by heating, and the aggregate 1s is This is by absorbing expansion. Therefore, in the case of casting with a mold using the foundry sand according to the present invention, no casting defects due to high temperature cracking occur, similar to Comparative Sand 1 using water glass as a caking agent. Note that 11 in Figure 3 (4) is an organic binder! 11' in 51E103) represents the carbide.

(2)崩壊性二 上記第2試験片をアルミ箔に包んで所定の温度に保った
炉中へ挿入し、1時間加熱した後炉冷して残留圧縮強度
を測定した。結果は第2図に示す通シであった。第2図
中1は比較砂1の、2#′i比較砂2の、5は本発明に
よる鋳物砂2の結果を示す。なお、本発明による鋳物砂
1も鋳物砂2と同様の結果が得られて−る。
(2) Collapsibility 2 The above second test piece was wrapped in aluminum foil and inserted into a furnace kept at a predetermined temperature, heated for 1 hour, then cooled in the furnace and the residual compressive strength was measured. The results were as shown in Figure 2. In FIG. 2, 1 indicates the results for comparative sand 1, 2#'i for comparative sand 2, and 5 for foundry sand 2 according to the present invention. Note that the same results as foundry sand 2 were obtained with foundry sand 1 according to the present invention.

崩壊性は、残留圧縮強度が低い程、良1とされている。The lower the residual compressive strength, the better the disintegration property.

第2図から明らかなように、比較砂1の場合、800〜
1000℃に加熱されると水ガラスが軟化し骨材を焼結
させて残留圧縮強度が高くなり、これが崩壊性不良の原
因となるのに対し、比較砂2の場合は、800℃以上に
加熱されると樹脂が炭化して強度が失われ、これが崩壊
性を良好とする原因となる。
As is clear from Figure 2, in the case of comparative sand 1, 800~
When heated to 1000°C, the water glass softens and sinters the aggregate, increasing the residual compressive strength, which causes poor collapsibility, whereas Comparative Sand 2 was heated to over 800°C. If this happens, the resin will carbonize and lose its strength, which will cause the disintegration to be good.

一方、本発明による鋳物砂2の場合、第2図から明らか
なように1水ガラスを使用してiるにもかかわらず、8
00℃以上の残留圧縮強度が低く、崩壊性が良好である
。これは第5図(4)、03)の模式図によって説明す
ると、骨材1sの表面の水ガラス12が高温で軟化溶融
しても、その周囲KN機系粘結材11の残渣炭化物11
′があるため、骨材1sの焼結が妨げられることによる
ものと推測される。
On the other hand, in the case of the foundry sand 2 according to the present invention, as is clear from FIG.
It has low residual compressive strength at temperatures above 00°C and has good disintegration properties. This can be explained using the schematic diagram in FIG. 5 (4), 03). Even if the water glass 12 on the surface of the aggregate 1s is softened and melted at high temperature, the residual carbide 11 of the surrounding KN mechanical caking material 11 remains.
It is presumed that this is because sintering of the aggregate 1s is hindered because of the presence of .

以上説明したように本発明鋳物砂によれば、(1)  
有機系粘結材を使用しt鋳型に水ガラスによる可縮性(
クッション性)を付与することによ〕、崩壊性を損うこ
となく、ペーニング、ベー二ングに起因する部層および
鋳物の高温割れ等の鋳造欠陥が防止でき、 (2)水ガラス′を着接した骨材の代シに、水クラス系
古砂を使用しても、同様の作用効果が得られ、これまで
裏砂和しか使用できなかった古#を中子としても使用す
ることができる。
As explained above, according to the foundry sand of the present invention, (1)
Using an organic binder, the mold is made of water glass (
By imparting cushioning properties], casting defects such as hot cracking of parts and castings caused by panning and vaning can be prevented without impairing collapsibility. Similar effects can be obtained by using water-class old sand as a substitute for the contacting aggregate, and old sand can also be used as a core, whereas until now only the back sand could be used. .

等の効果1mすることができる。The effect of 1m can be achieved.

【図面の簡単な説明】[Brief explanation of drawings]

$1111は各鋳物砂による鋳型の急熱膨張の経時変化
の実測値を示す図表、Wl、2図は各鋳物砂による鋳型
の各温度での加熱後炉冷した場合の残留圧縮強度の実測
値を示す凶表、第3−は本発明鋳物砂の構成を模式的に
示す因で、(6)が常温での状態、(6)が加熱後の状
態である。 11、理人萩原亮− 矛1図 加虱時向(剣
$1111 is a chart showing the actual measured value of the change in rapid thermal expansion of the mold with each molding sand over time, Wl, Figure 2 is the actual measured value of the residual compressive strength when the mold with each molding sand is heated at each temperature and then cooled in the furnace. Table 3 shows the structure of the foundry sand of the present invention, and (6) shows the state at room temperature and (6) shows the state after heating. 11. Rijin Ryo Hagiwara - Spear 1 Illustration Kagou Tokimuki (Sword

Claims (1)

【特許請求の範囲】[Claims] 耐火性骨材の表面に水ガラスを被橿したコーティングサ
ンドまたは水ガラス系古砂に有機系粘結材を添加混線し
てなる鋳物砂。   ゛
Coated sand with water glass coated on the surface of refractory aggregate, or foundry sand made by mixing old water glass sand with an organic caking agent added.゛
JP14250281A 1981-09-11 1981-09-11 Casting sand Pending JPS5844944A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14250281A JPS5844944A (en) 1981-09-11 1981-09-11 Casting sand

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14250281A JPS5844944A (en) 1981-09-11 1981-09-11 Casting sand

Publications (1)

Publication Number Publication Date
JPS5844944A true JPS5844944A (en) 1983-03-16

Family

ID=15316826

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14250281A Pending JPS5844944A (en) 1981-09-11 1981-09-11 Casting sand

Country Status (1)

Country Link
JP (1) JPS5844944A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012076115A (en) * 2010-10-01 2012-04-19 Lignyte Co Ltd Binder-coated refractory, casting mold, method for producing the casting mold
CN103272989A (en) * 2013-04-16 2013-09-04 繁昌县恒鑫汽车零部件有限公司 Molding sand manufactured from chromite sand as main material and manufacturing method thereof
CN104525842A (en) * 2014-12-01 2015-04-22 繁昌县恒鑫汽车零部件有限公司 Facing sand for casting of gray cast iron cylinder bodies and preparation method thereof
CN112775390A (en) * 2020-12-19 2021-05-11 郑州煤机格林材料科技有限公司 Mixed sand process replacing pure chromium ore sand

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012076115A (en) * 2010-10-01 2012-04-19 Lignyte Co Ltd Binder-coated refractory, casting mold, method for producing the casting mold
CN103272989A (en) * 2013-04-16 2013-09-04 繁昌县恒鑫汽车零部件有限公司 Molding sand manufactured from chromite sand as main material and manufacturing method thereof
CN104525842A (en) * 2014-12-01 2015-04-22 繁昌县恒鑫汽车零部件有限公司 Facing sand for casting of gray cast iron cylinder bodies and preparation method thereof
CN112775390A (en) * 2020-12-19 2021-05-11 郑州煤机格林材料科技有限公司 Mixed sand process replacing pure chromium ore sand

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