JPS60221146A - Resin-coated sand for casting - Google Patents

Resin-coated sand for casting

Info

Publication number
JPS60221146A
JPS60221146A JP7657184A JP7657184A JPS60221146A JP S60221146 A JPS60221146 A JP S60221146A JP 7657184 A JP7657184 A JP 7657184A JP 7657184 A JP7657184 A JP 7657184A JP S60221146 A JPS60221146 A JP S60221146A
Authority
JP
Japan
Prior art keywords
resin
sand
stearic acid
mold
mold release
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
JP7657184A
Other languages
Japanese (ja)
Inventor
Hitoshi Kimura
均 木村
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.)
Nissan Motor Co Ltd
Original Assignee
Nissan Motor 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 Nissan Motor Co Ltd filed Critical Nissan Motor Co Ltd
Priority to JP7657184A priority Critical patent/JPS60221146A/en
Publication of JPS60221146A publication Critical patent/JPS60221146A/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
    • B22C1/20Compositions 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 of organic agents
    • B22C1/22Compositions 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 of organic agents of resins or rosins
    • B22C1/2233Compositions 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 of organic agents of resins or rosins obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • B22C1/2266Polyesters; Polycarbonates

Landscapes

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

Abstract

PURPOSE:To improve the releasability from a molded metallic mold consisting of resin-coated sand by using a binder resin compsn. prepd. by adding a small amt. of silicone oil and stearic acid (metallic salt) to an unsatd. polyester resin. CONSTITUTION:The unsatd. polyester resin is used as an essential binder and is welded to molding sand; further the silicone oil which is a mold releasing agent is added in a heated state to the main binder at 1-3wt% by the weight thereof under agitation. >=1 kinds of the mold releasing agents consisting of the stearic acid and metallic salt of the stearic acid are in succession added at >=2% thereto and the mixing and agitation are continued to form the resin-coated sand. Such coated sand has good sand removability after casting and improves the releasability from the metallic mold when used as core sand.

Description

【発明の詳細な説明】 (発明の関連する技術分野) この発明は、アルミニウムに代表される低融点金属鋳物
の中子砂として使用される、鋳込み後、砂焼きを必要と
せず排砂可能な、易崩壊性の鋳物用樹脂被覆砂に関する
ものである。
Detailed Description of the Invention (Technical field to which the invention relates) The present invention is directed to a method of sand removal, which is used as core sand for casting low melting point metals such as aluminum, and which can be removed after casting without the need for sand baking. , relating to easily disintegrating resin-coated sand for foundry use.

(従来技術) 従来の易崩壊性の鋳物樹脂被覆砂としては、例えば特開
昭54−80284号、同54−162622号、同5
5−165250号、同55−165251号、同65
−165252号、同57−11’5988号公報に開
示されているような不飽和ポリエステ/I/w脂を主バ
インダーとして用いた樹脂組成物により被覆されたもの
がある。かかる儒脂組成物で被覆された樹脂被覆砂にあ
っては、樹脂の熱分解性が極めて高いため、アルミニウ
ム等の低融点金属鋳物の中子砂として使用した場合、鋳
込み後の排砂性が極めて良好であり、砂焼きを全く行な
わず、はぼ100チの排砂が可能なものである。
(Prior art) As conventional easily disintegrating foundry resin coated sand, for example, JP-A-54-80284, JP-A-54-162622, JP-A-5
No. 5-165250, No. 55-165251, No. 65
-165252 and No. 57-11'5988, which are coated with resin compositions using unsaturated polyester/I/w resin as the main binder. In resin-coated sand coated with such a Confucian fat composition, the thermal decomposition of the resin is extremely high, so when it is used as core sand for casting low-melting point metals such as aluminum, the sand dischargeability after casting is poor. It is very good, and it is possible to remove about 100 inches of sand without performing any sand burning.

しかしながら不飽和ポリエステル樹脂を主バインダーと
する樹脂組成物で被覆された樹脂被覆砂は、いずれも、
中子を成形する際、金型よりの脱型時に破損し、成形歩
留りが悪いという問題点を有していた。
However, resin-coated sand coated with a resin composition containing an unsaturated polyester resin as the main binder,
When molding the core, there was a problem in that it was damaged when removed from the mold, resulting in poor molding yield.

(発明の開示) この発明は、このような従来の問題点に着目してなされ
たもので、中子強度を上げるという従来の考え方とは全
く異なり、不飽和ポリエステル樹脂i主バインダーとし
て用いた、ホットメA/ト法による樹脂被覆砂作製時に
おいて、バインダー樹脂にシリコンオイル好ましくはジ
メチルシリコンオイル、ジフェニルシリコンオイルおよ
びメチルフェニルシリコンオイル(以下シリコン系離型
剤と称す)から成る群から選ばれた少くとも1種とステ
アリン酸およびステアリン酸金属塩(以下ステアリン酸
系離型剤と称す)から成る群から選ばれた少くとも1種
を添加して成るバインダー樹脂組成物を用いることによ
り、樹脂被覆砂の成形金型よりの離型性を改善せしめ上
記問題点を解決することを目的としている。
(Disclosure of the Invention) This invention was made by focusing on such conventional problems, and is completely different from the conventional idea of increasing core strength. When producing resin-coated sand by the hot metal A/T method, silicone oil, preferably a small amount selected from the group consisting of dimethyl silicone oil, diphenyl silicone oil and methylphenyl silicone oil (hereinafter referred to as silicone mold release agent), is added to the binder resin. By using a binder resin composition containing at least one selected from the group consisting of stearic acid and stearic acid metal salts (hereinafter referred to as stearic acid mold release agents), resin-coated sand can be produced. The purpose of this invention is to improve the mold releasability from the molding die and solve the above problems.

ホットメルト法により樹脂被覆砂を作成する場合、砂粒
同志のすべりを向上させ、砂づまりを良くするとともに
、金型よりの離型性を向上させることを目的として、ス
テアリン酸系離型剤を添加することが一般に行なわれて
いる。この離型機構は、加熱硬化時、ステアリン酸系離
型剤が溶融し、カルボン酸またはカルボン酸金属塩が金
型面に配向し、極性の低いステアリン酸のメチレン骨格
が・鋳型面に配向することによると推定される。ホット
メルト法に通常使用されるフェノール樹脂をノくインダ
ーとした場合は、ステアリン酸系離型剤とフェノール樹
脂の相溶性が乏しいため、加熱硬化時、ステアリン酸系
離型剤が、樹脂より遊離し金型面に配向し易いため、充
分な離型性を得ることができる。ところが、不飽和ポリ
エステル樹脂の場合、その骨格中に、エステル結合を有
している為、ステアリン酸系離型剤との相溶性が良好で
あり、加熱硬化時に、ステアリン酸系離型剤が樹脂より
遊離しに<<、充分に金型面に配向できず、充分な離型
性を得ることができない。一方樹脂成形体を作成する場
合、金型よりの離型性が特にめられる場合、シリコン系
離型剤を内添する方法は一般に良く知られている。樹脂
成形体の場合、樹脂層が連続しているため、比較的深い
層からも離型剤が金型面へ移行できるため、樹脂に対し
て少ない添加量で充分離型性を得ることが可能である。
When creating resin-coated sand using the hot melt method, a stearic acid-based mold release agent is added to improve the slippage between sand grains, improve sand clogging, and improve mold release from the mold. This is commonly done. This mold release mechanism is such that during heat curing, the stearic acid-based mold release agent melts, carboxylic acid or carboxylic acid metal salts are oriented to the mold surface, and the methylene skeleton of stearic acid, which has low polarity, is oriented to the mold surface. It is estimated that it is possible. When a phenolic resin, which is commonly used in the hot-melt method, is used as an inder, the stearic acid mold release agent and the phenolic resin have poor compatibility, so the stearic acid mold release agent is released from the resin during heat curing. Since it is easily oriented on the mold surface, sufficient mold releasability can be obtained. However, in the case of unsaturated polyester resin, it has ester bonds in its skeleton, so it has good compatibility with stearic acid-based mold release agents, and the stearic acid-based mold release agent is released into the resin during heat curing. If the particles are more loose than <<, they cannot be sufficiently oriented on the mold surface and sufficient mold releasability cannot be obtained. On the other hand, when producing a resin molded article, and when releasability from a mold is particularly important, a method of internally adding a silicone-based mold release agent is generally well known. In the case of resin moldings, since the resin layer is continuous, the mold release agent can migrate to the mold surface even from a relatively deep layer, so it is possible to obtain sufficient separability with a small amount added to the resin. It is.

しかし、樹脂被覆砂の場合、バインダー樹脂は、砂に対
して通常5重量−以下という少ない蓋7で使用され、樹
脂層は非連続であり、沸点の極め・て高いシリコン系離
型剤の場合には、金型に接した砂粒に被覆された極めて
少ない樹脂中に含まれる離型剤以外は、離型性に寄与し
ない。従って、樹脂被覆砂においては、シリコン系離型
剤のみを添加した場合には、殆んど離型性に効果が無い
という結果が得られる。
However, in the case of resin-coated sand, the binder resin is used in a small amount, usually less than 5% by weight relative to the sand, and the resin layer is discontinuous. In this case, only a very small amount of the mold release agent contained in the resin that coats the sand grains in contact with the mold contributes to mold releasability. Therefore, in the case of resin-coated sand, when only a silicone-based mold release agent is added, the result is that there is almost no effect on mold release properties.

しかるに驚くべきことには、この発明においてシリコン
系離型剤とステアリン酸系離型剤を組み合せて使用する
と、シリコン系離型剤によりステアリン酸系離型剤と不
飽和ポリエステルの相溶性が減ぜられ、この効果によっ
てステアリン酸系離型剤が金型表面に配向し易くなり、
本来の離型効果を充分に発揮させることができる。不飽
和ポリエステル樹脂へのシリコン系離型剤とステアリン
酸系離型剤の添加は、ステアリン酸系離型剤を前もって
添加すると、樹脂との相溶物を形成してしまい、非極性
のシリコン系離型剤がその外側をつつみこむ形となり、
本来の離型効果を示さなくなるので、シリコン系離型剤
は、ステアリン酸系離次にこの発明においてシリコン系
離型剤は、樹脂に対して1〜8重量重量油添加。1重量
−未満では、非相溶層の形成が充分でなく、このため離
型性向上の目的が達成されず、一方8重量%を越える場
合には、樹脂被覆時硬粒間で滑りを生じ、樹脂が砂表面
に均一に被覆される為の力がかかりにくくなる結果、硬
化後の鋳型強度が低下し、成形歩留りが悪くなり好まし
くない。ステアリン酸系離型剤は、後述の実施例で示す
ように樹脂に対して2重量%以上添加すればよく、上限
は特に限定されないが、一般には、10重量%以下で用
いられるのが普通である。
However, surprisingly, when a silicone-based mold release agent and a stearic acid-based mold release agent are used in combination in this invention, the silicone-based mold release agent reduces the compatibility between the stearic acid-based mold release agent and the unsaturated polyester. This effect makes it easier for the stearic acid-based mold release agent to align on the mold surface.
The original mold release effect can be fully exhibited. When adding a silicone-based mold release agent and a stearic acid-based mold release agent to unsaturated polyester resin, if the stearic acid-based mold release agent is added in advance, it will form a compatible solution with the resin, resulting in non-polar silicone-based mold release agents. The mold release agent wraps around the outside,
Since the silicone-based mold release agent no longer exhibits the original mold-releasing effect, the stearic acid-based silicone-based mold release agent is used.In the present invention, the silicone-based mold release agent is added to the resin by 1 to 8% oil by weight. If the amount is less than 1% by weight, the formation of an incompatible layer will not be sufficient and therefore the objective of improving mold releasability will not be achieved, while if it exceeds 8% by weight, slipping will occur between the hard particles during resin coating. This is undesirable because it becomes difficult to apply force to uniformly coat the resin on the sand surface, resulting in a decrease in mold strength after curing and poor molding yield. As shown in the examples below, the stearic acid-based mold release agent may be added in an amount of 2% by weight or more based on the resin, and the upper limit is not particularly limited, but it is generally used in an amount of 10% by weight or less. be.

この発明で用いられる不飽和ポリエステル樹脂としては
、例えばフマル酸、マレイン酸、無水マレイン酸等の不
飽和の二塩基酸を主とし、要すれば一部を無水フタル酸
等の飽和二塩基酸とし、エチレンf IJコール、プロ
ピレングリコール等のジオールとの間の重縮合反応によ
り得られる樹脂などを使用することができる。この際、
常温で固体である樹脂を用いたほうが、I#I脂被覆被
覆砂タつ、きが少なく、エアーブローにより金型に被覆
砂を詰めこむ場合、砂詰まりが良いため望ましいと言え
る。
The unsaturated polyester resin used in this invention is mainly composed of unsaturated dibasic acids such as fumaric acid, maleic acid, and maleic anhydride, and if necessary, contains a part of saturated dibasic acids such as phthalic anhydride. A resin obtained by a polycondensation reaction with a diol such as , ethylene f IJ col, propylene glycol, etc. can be used. On this occasion,
It is preferable to use a resin that is solid at room temperature because the I#I fat-coated sand is less likely to tack and scratch, and when the mold is filled with the sand coated by air blowing, the sand is more likely to clog.

(発明の実施例) 次にこの発明を実施例、比較例および試験例により説明
する。
(Examples of the Invention) Next, the present invention will be explained with reference to Examples, Comparative Examples, and Test Examples.

実施例1〜8.比較例1〜10 万能混合攪拌式5 DWM (品用工業所製)に、17
0’Cに加熱した日光珪砂5号1000gを投入した後
、攪拌しながら、10メツシユ以下に粉砕した不飽和ポ
リエステル樹脂ニスターN +3000(三井東圧化学
(株)製)25gを加えて混合溶融させ、砂の表面に融
着させた。更に砂温180℃の状態で、n−ヘキサン5
gに、tert−ブチルパーオキシベンゾエート0.3
9 、シクロヘキサノンパーオキサイドo、s9、α−
メタクリルオキシプロピルトリメチルシラン(日本ユニ
カー(株) 製A −174) 0.59および第1表
に示すシリコン系離型剤を所定量溶解したものを混合し
、攪拌を続け、砂温70°Cになった時点で第1表に示
すステアリン酸系離型剤を添加し、各樹脂被覆砂を得た
Examples 1-8. Comparative Examples 1 to 10 Universal mixing stirring type 5 DWM (manufactured by Shinyo Kogyo Co., Ltd.), 17
After adding 1000 g of Nikko silica sand No. 5 heated to 0'C, while stirring, add 25 g of unsaturated polyester resin Nister N +3000 (manufactured by Mitsui Toatsu Chemical Co., Ltd.) crushed to 10 mesh or less and mix and melt. , fused to the sand surface. Furthermore, with the sand temperature at 180°C, 5
g, tert-butyl peroxybenzoate 0.3
9, cyclohexanone peroxide o, s9, α-
Methacryloxypropyltrimethylsilane (A-174 manufactured by Nippon Unicar Co., Ltd.) 0.59 and a predetermined amount of the silicone-based mold release agent shown in Table 1 were mixed and stirred, and the sand temperature was raised to 70°C. At this point, a stearic acid-based mold release agent shown in Table 1 was added to obtain each resin-coated sand.

比較例11〜】4 万能混合攪拌m 5 DWM (品用工業所製)に、1
70°Cに加熱した日光珪砂5号1000gを投入し、
攪拌しなから1oメツシユ以下に粉砕した不飽和ポリエ
ステル樹脂N8000 21と、第1表に示すステアリ
ン酸系離型剤の所定量を同時に加えて混合溶融させ、砂
の表面に融着させた。更に砂温180℃の状態で、n−
ヘキサン5gにtert −ブチルパーオキシベンゾエ
ート0.8g、シクロヘキサノンパーオキサイドo、a
 g 、α−メタクリルオキシプロピルトリメチルシラ
ン(日本:s−二カー (株)製、A −174) 0
.59および第1表に示すシリコン系離型剤を所定量溶
解したものを混合し、砂温70°C以下まで攪拌を続け
、樹脂被覆砂を得た。
Comparative Example 11 ~] 4 Universal mixing stirring m 5 DWM (manufactured by Shinyo Kogyo Co., Ltd.), 1
Add 1000g of Nikko silica sand No. 5 heated to 70°C,
Without stirring, unsaturated polyester resin N8000 21 pulverized to 10 mesh or less and a predetermined amount of a stearic acid mold release agent shown in Table 1 were simultaneously added, mixed and melted, and fused to the surface of the sand. Furthermore, at a sand temperature of 180℃, n-
0.8 g of tert-butyl peroxybenzoate in 5 g of hexane, cyclohexanone peroxide o, a
g, α-methacryloxypropyltrimethylsilane (Japan: S-Nika Co., Ltd., A-174) 0
.. A predetermined amount of the silicone-based mold release agent shown in Table 1 and No. 59 was mixed and stirred until the sand temperature reached 70° C. or lower to obtain resin-coated sand.

試験例 実施例1〜8.比較例1〜14の樹脂被覆砂を、JIS
K 6910−1964に準じ、曲げ強度測定に供した
。この際、試験片作製用金型を予め280″Cに加熱し
ておき、そこへ上記樹脂被覆砂を充填し〜280°Cで
70秒間放置して硬化を完了させた後、直ちに曲げ強度
を測定した。温時曲げ強度また金型離型性を測定する目
的で、テーパー付円筒状金型(高さ一5Qu+、上端部
内径b−28,4III+1下端部内径C−80,21
111)に、樹脂被覆砂を充填し、210″Cで70秒
間放置し硬化させた後、高滓製作所製万能引張試験機(
オートグラフ)にて、小口径側より荷重をかけ、鋳型を
離型するに要した荷重を測定した。得られた「抜き抵抗
」結果を第1表に併記する。
Test Examples Examples 1-8. The resin-coated sand of Comparative Examples 1 to 14 was
It was subjected to bending strength measurement according to K 6910-1964. At this time, the mold for preparing the test piece was preheated to 280"C, the resin-coated sand was filled into it, and the resin-coated sand was left at ~280°C for 70 seconds to complete curing, and then the bending strength was immediately measured. In order to measure the bending strength at temperature and the mold releasability, a tapered cylindrical mold (height 15 Qu+, upper end inner diameter B-28, 4III+1 lower end inner diameter C-80, 21
111) was filled with resin-coated sand, left to harden at 210"C for 70 seconds, and then tested using a universal tensile tester manufactured by Takashi Seisakusho (
Autograph), a load was applied from the small diameter side and the load required to release the mold was measured. The obtained "pull resistance" results are also listed in Table 1.

(発明の効果) 以上説明してきたように、この発明の鋳物用樹脂被覆砂
は、不飽和ポリエステル樹脂にシリコン糸離型剤とステ
アリン酸系離型剤を添加して成るバインダー樹脂組成物
で被覆されているため、中子砂として使用した場合、鋳
込み後の排砂性が良好なることは勿−のこと、金型より
の離型性が改善され成形歩留りが良好であるという効果
が得られる。
(Effects of the Invention) As explained above, the resin-coated sand for foundries of the present invention is coated with a binder resin composition made by adding a silicone thread mold release agent and a stearic acid mold release agent to an unsaturated polyester resin. Therefore, when used as core sand, it not only improves the sand removal performance after casting, but also improves the releasability from the mold and improves the molding yield. .

特許出願人 日産自動車株式会社Patent applicant: Nissan Motor Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] L 不飽和ポリエステル樹脂を主バインダーとして用い
、このバインダー樹脂に対して、シリコンオイ/l/1
〜8重量%添加し、次いでステアリン酸およびステアリ
ン酸金属塩から成る群から選ばれた少くとも1種を2重
量−以上添加して成るバインダー樹脂組成物により被覆
されたことを特徴とする鋳物用樹脂被覆砂。
L Unsaturated polyester resin is used as the main binder, and silicone oil/l/1 is added to this binder resin.
- 8% by weight, and then at least 2% by weight of at least one selected from the group consisting of stearic acid and metal stearate. Resin coated sand.
JP7657184A 1984-04-18 1984-04-18 Resin-coated sand for casting Pending JPS60221146A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7657184A JPS60221146A (en) 1984-04-18 1984-04-18 Resin-coated sand for casting

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7657184A JPS60221146A (en) 1984-04-18 1984-04-18 Resin-coated sand for casting

Publications (1)

Publication Number Publication Date
JPS60221146A true JPS60221146A (en) 1985-11-05

Family

ID=13608917

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7657184A Pending JPS60221146A (en) 1984-04-18 1984-04-18 Resin-coated sand for casting

Country Status (1)

Country Link
JP (1) JPS60221146A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100704126B1 (en) 2006-04-21 2007-04-09 지주건설 주식회사 Releasing agent for color concrete and production method
CN103551493A (en) * 2013-11-13 2014-02-05 中国石油集团济柴动力总厂成都压缩机厂 Resin sand for casting shape and sand core of natural gas power cylinder body
CN104325065A (en) * 2014-10-08 2015-02-04 吴江市液铸液压件铸造有限公司 Coated sand and preparation method thereof
CN108296421A (en) * 2017-10-27 2018-07-20 柳州市柳晶科技股份有限公司 Precoated sand for 3D printing
CN108772534A (en) * 2018-06-26 2018-11-09 重庆长江造型材料(集团)股份有限公司 A kind of precoated sand and preparation method thereof

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100704126B1 (en) 2006-04-21 2007-04-09 지주건설 주식회사 Releasing agent for color concrete and production method
CN103551493A (en) * 2013-11-13 2014-02-05 中国石油集团济柴动力总厂成都压缩机厂 Resin sand for casting shape and sand core of natural gas power cylinder body
CN104325065A (en) * 2014-10-08 2015-02-04 吴江市液铸液压件铸造有限公司 Coated sand and preparation method thereof
CN108296421A (en) * 2017-10-27 2018-07-20 柳州市柳晶科技股份有限公司 Precoated sand for 3D printing
CN108772534A (en) * 2018-06-26 2018-11-09 重庆长江造型材料(集团)股份有限公司 A kind of precoated sand and preparation method thereof

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