JPH01271054A - Production of casting - Google Patents

Production of casting

Info

Publication number
JPH01271054A
JPH01271054A JP9750588A JP9750588A JPH01271054A JP H01271054 A JPH01271054 A JP H01271054A JP 9750588 A JP9750588 A JP 9750588A JP 9750588 A JP9750588 A JP 9750588A JP H01271054 A JPH01271054 A JP H01271054A
Authority
JP
Japan
Prior art keywords
casting
mold
carbon film
carbon
organic binder
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
JP9750588A
Other languages
Japanese (ja)
Other versions
JP2905205B2 (en
Inventor
Hitoshi Funada
等 船田
Kazuhiko Kiuchi
一彦 木内
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.)
Kao Corp
Original Assignee
Kao Corp
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 Kao Corp filed Critical Kao Corp
Priority to JP63097505A priority Critical patent/JP2905205B2/en
Publication of JPH01271054A publication Critical patent/JPH01271054A/en
Application granted granted Critical
Publication of JP2905205B2 publication Critical patent/JP2905205B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To prevent roughening surface on the casting surface even if facing agent is saved by pouring the specific temp. of molten metal into a mold manufactured with binder containing organic binder as main component, developing carbon film having the specific characteristic on interface and casting. CONSTITUTION:The molten metal having 1200-1800 deg.C is poured into the mold with the binder, and by developing the carbon film having the undermentioned characteristic on the interface between the mold and the casting, it is cast. (1) Raman spectrum of the carbon film has bends at 1330-1390cm<-1> and 1550-1630cm<-1> and relative intensity is 0.5-2.0. (2) Face interval in (002) face of carbon with X ray diffraction of the carbon film is 3.35-4.25Angstrom . The relative intensity for two bands is the ratio (B/A) of 1330-1390cm<-1> band height B from the base line to 1550-1630cm<-1> band height A. The organic binder uses fran resin, phenol resin and is desirable to add pitch, tar, etc. By this method, the roughening surface of the casting surface without using heat resistant film on the mold surface, that is, the facing agent, can be prevented.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、無塗型で平滑な鋳肌を得る鋳物製造法に関す
る。更に詳しくは、鋳型と鋳物の界面に炭素膜を形成さ
せることにより塗型を全く必要としないか、あるいはほ
とんど必要としないで平滑な鋳肌を得る鋳物製造法に関
するものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a casting manufacturing method for obtaining a smooth casting surface using an uncoated mold. More specifically, the present invention relates to a casting manufacturing method that obtains a smooth casting surface with no or little need for coating by forming a carbon film at the interface between the mold and the casting.

〔従来の技術〕[Conventional technology]

鋳造用鋳型に対しては、従来から溶融金属が鋳型を形成
する砂粒子の間隙中に浸入し、鋳物表面が粗面化するの
を防止するために鋳型を造型してから塗型剤を塗布して
いた。これらの塗型剤は刷毛塗り、スプレー、浸漬など
の方法によって塗布されている。
Conventionally, for casting molds, a coating agent is applied after the mold is formed to prevent molten metal from penetrating into the gaps between the sand particles forming the mold and roughening the surface of the casting. Was. These coating agents are applied by methods such as brushing, spraying, and dipping.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

塗型剤の塗布方法としては、−船釣には刷毛塗り、スプ
レーが比較的多く用いられているが、何れも塗型の膜厚
を均一にすることが困難であり、鋳物表面に刷毛目ある
いは凹凸ができたりする。また、この塗型作業は作業能
率向上の点からも好ましくなく、また鋳型製作費のコス
トアップにつながるという問題があった。
As for the coating method, - Brushing and spraying are relatively often used for boat fishing, but in both cases it is difficult to make the film thickness of the coating uniform, and brush marks appear on the surface of the casting. Or it may become uneven. Further, this mold coating operation is not preferable from the viewpoint of improving work efficiency, and there is also a problem in that it leads to an increase in mold manufacturing costs.

〔課題を解決するための手段〕[Means to solve the problem]

本発明者らは上記の課題を解決するために、塗型を全く
必要としないか、あるいはほとんど必要としない鋳物製
造法を提供することを目的とし鋭意研究を行った結果、
鋳造時に鋳型と鋳物の界面に特定の物性を有する炭素膜
を形成させることにより前記の課題を解決し得ることを
見出し、本発明を完成するに到った。
In order to solve the above problems, the present inventors conducted extensive research with the aim of providing a casting manufacturing method that does not require coating molds at all or hardly requires them.
The inventors have discovered that the above-mentioned problems can be solved by forming a carbon film having specific physical properties at the interface between the mold and the cast material during casting, and have completed the present invention.

即ち、本発明は、有機粘結剤を主成分とする粘結剤によ
り造型された鋳型に1200°C〜1800°Cの溶湯
を注入し、鋳型と鋳物との界面に下記特性を有する炭素
膜を生成させながら鋳造することを特徴とする鋳物製造
法。
That is, in the present invention, a molten metal at 1200°C to 1800°C is poured into a mold formed using a binder mainly composed of an organic binder, and a carbon film having the following characteristics is formed at the interface between the mold and the casting. A casting manufacturing method characterized by casting while producing.

(1)炭素膜のラマン分光スペクトルが1330〜13
90cm−’と1550〜1630ca+−’にバンド
を持ち、その相対強度が0.5〜2.01好ましくは0
.8〜1.3である。
(1) The Raman spectrum of the carbon film is 1330-13
It has bands at 90 cm-' and 1550 to 1630 ca+-', and its relative intensity is 0.5 to 2.01, preferably 0.
.. It is 8 to 1.3.

(2)炭素膜のX線回折による炭素の(002)面の面
間隔が3.35〜4.25人、好ましくは3.40〜3
.90人である。
(2) The interplanar spacing of the (002) plane of carbon as determined by X-ray diffraction of the carbon film is 3.35 to 4.25, preferably 3.40 to 3.
.. There are 90 people.

本発明において、鋳型と鋳物との界面に生成させる上記
の如き特性を有する炭素膜は、部分的に結晶化した炭素
の連続薄層であり、かかる薄層の生成により上記の如き
本発明の目的が達成される。
In the present invention, the carbon film having the above-mentioned characteristics formed at the interface between the mold and the casting is a continuous thin layer of partially crystallized carbon, and the formation of such a thin layer achieves the above-mentioned objects of the present invention. is achieved.

尚、本発明において、ラマン分光スペクトルの2つのバ
ンドの相対強度とは、第1図の如く1000〜1800
cm−’にかけてのベースラインからの1330〜13
90cm−’バンドの高さ(B)の1550〜1630
cm−’バンドの高さ(A)に対する比(B/A)であ
る。
In addition, in the present invention, the relative intensity of two bands of the Raman spectroscopic spectrum is 1000 to 1800 as shown in Figure 1.
1330-13 from baseline over cm-'
90cm-' band height (B) 1550-1630
cm-' is the ratio (B/A) to the height (A) of the band.

ラマン分光スペクトルは、日本分光社製レーザーラマン
スペクトル測定装置を用い、レーザー源に20抛−15
14,5n11のアルゴンレーザーを使用して測定した
Raman spectra were measured using a laser Raman spectrum measurement device manufactured by JASCO Corporation, with a laser source of 20-15 mm.
Measurements were made using a 14,5n11 argon laser.

また本発明において、炭素の(002)面の面間隔とは
、002回折線の回折角から、次の式(1)に示すブラ
ックの式で求めた値である。
Further, in the present invention, the interplanar spacing of the (002) plane of carbon is a value determined from the diffraction angle of the 002 diffraction line using Black's equation shown in the following equation (1).

2dsinθ−λ ・(1) (式中、dは面間隔、θは回折角、λはX線の波長であ
る。) 本発明において、X線回折は、理学社製薄膜X線回折装
置(TFDシステム)を用い、Cuα線を用い、入射角
0.2°、管電圧50kV、管電流100+*Aにて測
定した。
2dsinθ−λ ・(1) (In the formula, d is the interplanar spacing, θ is the diffraction angle, and λ is the wavelength of the X-ray.) In the present invention, X-ray diffraction is performed using a thin film X-ray diffraction device (TFD) manufactured by Rigakusha. Measurement was carried out using Cuα rays at an incident angle of 0.2°, a tube voltage of 50 kV, and a tube current of 100+*A.

本発明に用いられる有機粘結剤は、フラン樹脂、フェノ
ール樹脂などの粘結剤が使用されるが、高周波誘導加熱
法、例えばキューリーポイントパイロライザ(日本分析
工業■製)により、不活性ガス、例えばヘリウムガス雰
囲気下1000〜1050°Cに急速加熱した時に、ベ
ンゼンやトルエン、エチルベンゼン、エチルトルエン、
キシレン、クレゾール、キシレノール等のメチル基ある
いはエチル基などで置換された芳香族化合物を多く発生
するような有機粘結剤が好ましい。
The organic binder used in the present invention is furan resin, phenol resin, etc., but it is possible to use an inert gas, For example, when rapidly heated to 1000-1050°C in a helium gas atmosphere, benzene, toluene, ethylbenzene, ethyltoluene, etc.
Organic binders that generate a large amount of aromatic compounds substituted with methyl groups or ethyl groups, such as xylene, cresol, and xylenol, are preferred.

また硬化反応には寄与しないが、ピッチ、タールなどを
添加することも好ましい。尚、有機粘結剤の添加量は1
00重量部の耐火性粒状材料に対して0.5〜6重量部
が好ましい。
It is also preferable to add pitch, tar, etc., although they do not contribute to the curing reaction. The amount of organic binder added is 1
0.5 to 6 parts by weight per 00 parts by weight of refractory granular material are preferred.

また、上記有機粘結剤を硬化させる方法としては、自硬
性及びガス硬化性コールドボックス等がある。自硬性鋳
型法の硬化剤としては、パラトルエンスルホン酸、キシ
レンスルホン酸等の有機スルホン酸や、リン酸、硫酸等
の無機酸やこれらの混合物が使用される。また、酸硬化
性コールドボックス法の過酸化物としては、ケトン系、
芳香族系等の有機過酸化物及び過酸化水素等の無機過酸
化物が使用される。これらの硬化剤及び過酸化物の添加
量は100重量部の有機粘結剤に対して、10〜70重
量部が好ましい。
Furthermore, methods for curing the organic binder include self-hardening and gas-hardening cold boxes. As the hardening agent for the self-hardening mold method, organic sulfonic acids such as para-toluenesulfonic acid and xylene sulfonic acid, inorganic acids such as phosphoric acid and sulfuric acid, and mixtures thereof are used. In addition, peroxides for the acid-curing cold box method include ketones,
Organic peroxides such as aromatic ones and inorganic peroxides such as hydrogen peroxide are used. The amount of these curing agents and peroxides added is preferably 10 to 70 parts by weight per 100 parts by weight of the organic binder.

本発明に用いられる鋳型を構成する耐火性粒状材料とし
ては、石英質を主成分とする珪砂の他、ジルコン砂、ク
ロマイト砂等が使用される。
As the refractory granular material constituting the mold used in the present invention, silica sand containing quartz as a main component, zircon sand, chromite sand, etc. are used.

また、鋳物の平滑性を得る目的以外の機能を付与するた
めに、Mg’O,CaC0a等の浸硫防止剤、鋳型強度
を向上させる為に、γ−アミノプロピルトリメトキシシ
ラン等の公知の各種シランカップリング剤などの添加剤
を鋳型中へ混合することも可能である。
In addition, in order to provide functions other than the purpose of obtaining smoothness of castings, sulfurization inhibitors such as Mg'O and CaC0a are used, and various known agents such as γ-aminopropyltrimethoxysilane are used to improve mold strength. It is also possible to mix additives into the mold, such as silane coupling agents.

更に、従来より鋳型の構成を溶湯に接触する肌砂部とそ
の内部の裏砂部に分割し、肌砂に粒度の細かい耐火骨材
を用い、塗型工程を省略する鋳型・鋳物製造法が知られ
ているが、本発明における炭素膜をこの肌砂に形成させ
ることにより、更に鋳肌の平滑性を向上させることも、
またより粒度の粗い骨材の使用を可能ならしめることも
出来る。本発明においては上記のようにして造型された
比較的多量の炭素源を含む鋳型に1200〜1800°
Cの溶湯を注入する際の熱により炭素源が分解し、鋳型
と鋳物の界面に、一部活晶化した炭素膜が生成すると考
えられる。
Furthermore, conventional methods of manufacturing molds and castings have been developed in which the structure of the mold is divided into a skin sand part that comes into contact with the molten metal and a back sand part inside the mold, and fine-grained refractory aggregate is used for the skin sand, and the mold coating process is omitted. Although it is known, by forming a carbon film on this skin sand in the present invention, it is also possible to further improve the smoothness of the casting surface.
It also allows the use of coarser aggregates. In the present invention, the mold containing a relatively large amount of carbon source formed as described above is heated at 1200 to 1800°.
It is thought that the heat generated when pouring the molten C decomposes the carbon source, and a partially activated crystallized carbon film is generated at the interface between the mold and the casting.

〔実施例〕〔Example〕

以下に実施例及び比較例を挙げて本発明を具体的に説明
するが、本発明はこれらの実施例のみに限定されるもの
ではない。又、実施例、比較例中、「部」とあるのはす
べて重量部である。
EXAMPLES The present invention will be specifically explained below with reference to Examples and Comparative Examples, but the present invention is not limited only to these Examples. Furthermore, in Examples and Comparative Examples, "parts" are all parts by weight.

実施例1 フルフリルアルコール39部に0−タレゾールノボラッ
クのグリシジルエーテル(住友化学■製「スミエポキシ
ESCN−220−10J )49部及び1゜2.4−
トリメリット酸トリアリルエステル11部を加え溶解し
て有機粘結剤とした。
Example 1 39 parts of furfuryl alcohol, 49 parts of glycidyl ether of 0-talesol novolak (Sumi Epoxy ESCN-220-10J manufactured by Sumitomo Chemical) and 1°2.4-
11 parts of trimellitic acid triallyl ester was added and dissolved to obtain an organic binder.

鋳物砂(フラタリー砂)100重量部に対し、上記有機
粘結剤を2部と60%−キシレンスルホン酸0.2部を
2分間撹拌し、鋳型を製作した。
To 100 parts by weight of foundry sand (flattery sand), 2 parts of the above organic binder and 0.2 part of 60% xylene sulfonic acid were stirred for 2 minutes to produce a mold.

この鋳型に1350℃の溶湯(FC−20相当)を注入
して得た鋳物の表面粗さを測定し、形成した炭素膜の分
析を行った。
A 1350°C molten metal (equivalent to FC-20) was poured into this mold, and the surface roughness of the casting obtained was measured, and the formed carbon film was analyzed.

その結果を表−1に示した。尚、表面粗さは鋳物各部1
4点の中心線平均粗さ(Ra)の平均をとった。
The results are shown in Table-1. In addition, the surface roughness of each part of the casting 1
The center line average roughness (Ra) of the four points was averaged.

実施例2 有機粘結剤として、フルフリルアルコール80部にアセ
ナフチレン20部を加え溶解したものを用いた以外は実
施例1と同様にして鋳型を製作し、実施例1と同様に鋳
込みを行って鋳物を得た。
Example 2 A mold was produced in the same manner as in Example 1, except that a solution of 20 parts of acenaphthylene added to 80 parts of furfuryl alcohol was used as the organic binder, and casting was performed in the same manner as in Example 1. I got a casting.

得られた鋳物の表面粗さの測定及び炭素膜の分析を実施
例1と同様に行った。
Measurement of the surface roughness of the obtained casting and analysis of the carbon film were carried out in the same manner as in Example 1.

結果を表−1に示す。The results are shown in Table-1.

実施例3 キシレン39部に0−タレゾールノボラックのグリシジ
ルエーテル(住友化学■製「スミエポキシESCN−2
20−10」)49部及び1,2.4− トリメリット
酸トリアリルエステル11部を加え溶解したものを有機
粘結剤として用い、60%−キシレンスルホン酸の代わ
りにクメンハイドロパーオキサイド0.3部を用い、S
O□ガスをガツシングする以外は実施例1と同様にして
鋳型を製作し、実施例1と同様に鋳込みを行って鋳物を
得た。
Example 3 Glycidyl ether of 0-talesol novolak ("Sumiepoxy ESCN-2" manufactured by Sumitomo Chemical ■) was added to 39 parts of xylene.
20-10'') and 11 parts of 1,2.4-trimellitic acid triallyl ester were added and dissolved and used as an organic binder, and 0.0% of cumene hydroperoxide was added instead of 60%-xylene sulfonic acid. Using 3 parts, S
A mold was manufactured in the same manner as in Example 1 except for gassing O□ gas, and casting was performed in the same manner as in Example 1 to obtain a casting.

得られた鋳物の表面粗さ測定及び炭素膜の分析を実施例
1と同様に行った。
The surface roughness measurement of the obtained casting and the analysis of the carbon film were carried out in the same manner as in Example 1.

結果を表−1に示す。The results are shown in Table-1.

比較例1及び2 鋳物砂(フラタリー砂)100重量部に対し、一般のフ
ラン樹脂(花王りエーカー鞠製r340B、 )1.2
部、60%−キシレンスルホン酸0.48部ヲ有機粘結
剤として用いる以外は実施例1と同様にして鋳型を製作
したものを比較例1、またその鋳型に塗型を塗布したも
のを比較例2とし、実施例1と同様に鋳込みを行って鋳
物を得た。
Comparative Examples 1 and 2 1.2 parts of general furan resin (R340B manufactured by Kao Acre Mari) was added to 100 parts by weight of foundry sand (flattery sand).
In Comparative Example 1, a mold was prepared in the same manner as in Example 1 except that 0.48 part of 60%-xylene sulfonic acid was used as the organic binder. As Example 2, casting was performed in the same manner as in Example 1 to obtain a casting.

得られた鋳物の表面粗さを実施例1と同様に測定した。The surface roughness of the obtained casting was measured in the same manner as in Example 1.

結果を表−1に示す。The results are shown in Table-1.

尚、比較例1及び2においては炭素膜は生成していなか
った。
Note that in Comparative Examples 1 and 2, no carbon film was formed.

表  −1 〔発明の効果〕 従来は、鋳型表面に耐熱性皮膜、即ち塗型を塗布し、鋳
型を形成する砂粒子の間隙中への溶融金属の浸入あるい
は骨材等の鋳型成分との融着により発生する鋳物表面の
粗面化を防止している。
Table 1 [Effects of the Invention] Conventionally, a heat-resistant film, that is, a coating mold, was applied to the surface of the mold to prevent molten metal from penetrating into the gaps between the sand particles forming the mold or fusion with mold components such as aggregate. This prevents the casting surface from becoming rough due to adhesion.

しかしながら、本発明により、上記塗型を全くあるいは
ほとんど省略しても鋳物の表面の粗面化を防止あるいは
改善することができ、鋳造工程の大幅な改善が可能とな
る。
However, according to the present invention, roughening of the surface of the casting can be prevented or improved even if the coating mold is completely or almost completely omitted, and the casting process can be significantly improved.

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

第1図は炭素膜のラマン分光スペクトル図である。 出願人代理人  古 谷   馨 第  1  図 波  数(帰−工) FIG. 1 is a Raman spectrogram of a carbon film. Applicant's agent Kaoru Furutani Figure 1 Number of waves (return)

Claims (1)

【特許請求の範囲】 1、有機粘結剤を主成分とする粘結剤により造型された
鋳型に1200℃〜1800℃の溶湯を注入し、鋳型と
鋳物との界面に下記特性を有する炭素膜を生成させなが
ら鋳造することを特徴とする鋳物製造法。 (1)炭素膜のラマン分光スペクトルが1330〜13
90cm^−^1と1550〜1630cm^−^1に
バンドを持ち、その相対強度が0.5〜2.0である。 (2)炭素膜のX線回折による炭素の(002)面の面
間隔が3.35〜4.25Åである。 2、炭素膜のラマン分光スペクトルの1330〜139
0cm^−^1と1550〜1630cm^−^1の各
バンドの相対強度が0.8〜1.3である請求項1記載
の製造法。
[Claims] 1. Molten metal at 1200°C to 1800°C is poured into a mold made with a binder mainly composed of an organic binder, and a carbon film having the following characteristics is formed at the interface between the mold and the casting. A casting manufacturing method characterized by casting while producing. (1) The Raman spectrum of the carbon film is 1330-13
It has bands at 90 cm^-^1 and 1550 to 1630 cm^-^1, and their relative intensities are 0.5 to 2.0. (2) The interplanar spacing of the (002) plane of carbon as determined by X-ray diffraction of the carbon film is 3.35 to 4.25 Å. 2. Raman spectrum of carbon film 1330-139
The manufacturing method according to claim 1, wherein the relative intensity of each band of 0 cm^-^1 and 1550 to 1630 cm^-^1 is 0.8 to 1.3.
JP63097505A 1988-04-20 1988-04-20 Casting manufacturing method Expired - Fee Related JP2905205B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63097505A JP2905205B2 (en) 1988-04-20 1988-04-20 Casting manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63097505A JP2905205B2 (en) 1988-04-20 1988-04-20 Casting manufacturing method

Publications (2)

Publication Number Publication Date
JPH01271054A true JPH01271054A (en) 1989-10-30
JP2905205B2 JP2905205B2 (en) 1999-06-14

Family

ID=14194118

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63097505A Expired - Fee Related JP2905205B2 (en) 1988-04-20 1988-04-20 Casting manufacturing method

Country Status (1)

Country Link
JP (1) JP2905205B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100422244B1 (en) * 1997-08-13 2004-03-10 나노-프로프리어터리, 인크. A carbon film for field emission devices

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5948062A (en) * 1982-09-10 1984-03-19 Maruichi Suisan Kk Apparatus for processing shrimp for sushi topping
JPS6228041A (en) * 1985-07-29 1987-02-06 Kao Corp Binder composition for casting

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5948062A (en) * 1982-09-10 1984-03-19 Maruichi Suisan Kk Apparatus for processing shrimp for sushi topping
JPS6228041A (en) * 1985-07-29 1987-02-06 Kao Corp Binder composition for casting

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100422244B1 (en) * 1997-08-13 2004-03-10 나노-프로프리어터리, 인크. A carbon film for field emission devices

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