Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPS6015417B2 - Coated sand composition for light alloy casting - Google Patents
[go: Go Back, main page]

JPS6015417B2 - Coated sand composition for light alloy casting - Google Patents

Coated sand composition for light alloy casting

Info

Publication number
JPS6015417B2
JPS6015417B2 JP4383483A JP4383483A JPS6015417B2 JP S6015417 B2 JPS6015417 B2 JP S6015417B2 JP 4383483 A JP4383483 A JP 4383483A JP 4383483 A JP4383483 A JP 4383483A JP S6015417 B2 JPS6015417 B2 JP S6015417B2
Authority
JP
Japan
Prior art keywords
coated sand
light alloy
parts
sand
alloy casting
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
Application number
JP4383483A
Other languages
Japanese (ja)
Other versions
JPS59189030A (en
Inventor
恭介 松藤
永治 錦織
俊忠 尾野田
道法 八坂
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.)
Matsuda KK
Original Assignee
Matsuda KK
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 Matsuda KK filed Critical Matsuda KK
Priority to JP4383483A priority Critical patent/JPS6015417B2/en
Publication of JPS59189030A publication Critical patent/JPS59189030A/en
Publication of JPS6015417B2 publication Critical patent/JPS6015417B2/en
Expired 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
    • B22C1/2246Condensation polymers of aldehydes and ketones
    • B22C1/2253Condensation polymers of aldehydes and ketones with phenols

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)

Description

【発明の詳細な説明】 本発明は、鋳造鋳型として使用される表面に樹脂を被覆
したコーテッドサンド、特に軽合金鋳物用のコーテッド
サンド組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a coated sand whose surface is coated with a resin to be used as a casting mold, and particularly to a coated sand composition for light alloy casting.

例えば、エンジンのシリンダヘツド等の内部構造の複雑
な製品を鋳造する場合に使用される中子は、注湯時には
湯の圧力に十分耐えられるだけの強度を維持し、且つ鋳
込み後における崩壊性が良好でなければならない。
For example, the cores used when casting products with complex internal structures, such as engine cylinder heads, must maintain sufficient strength to withstand the pressure of the hot metal during pouring, and be resistant to collapse after pouring. Must be in good condition.

そこで、この種の中子としては従来からコーテッドサン
ドと称せられる鋳物砂が使用されている。これは、鋳物
砂の表面を、粘緒剤として用いられるフェノール樹脂等
によってコーティングしたものである。しかし、従来の
コーテッドサンドは、鏡込温度の高い鋳鉄等の場合にお
いては比較的良好な崩壊性を示すものの、アルミニウム
やアルミニウム合金等の錆込温度の低い金属で鋳造する
場合は、崩壊性が充分でなく、鋳込み後の砂落し、特に
中子の排出に手間取るという欠点を有していた。
Therefore, foundry sand called coated sand has conventionally been used as this type of core. This is made by coating the surface of foundry sand with a phenol resin or the like used as a sticky agent. However, although conventional coated sand shows relatively good disintegration properties when cast iron has a high mirroring temperature, it has poor disintegration properties when cast with metals with low rusting temperatures such as aluminum and aluminum alloys. It was not sufficient and had the disadvantage that it took time to remove sand after casting, especially to eject the core.

このような実情に対処するものとしては、例えば特開昭
57一149043号に開示された「軽合金鋳造用のシ
ェルモールド鋳型材料」に関する発明が存在する。これ
は、鋳物砂100重量部を基準として、フェノール樹脂
0.3〜7重量部と、加熱することによりBrもしくは
Br化合物を分裂するBr含有有機化合物0.001〜
7重量部とからなる組成物を上記鋳物砂に被覆すること
を特徴とするもので、臭素含有有機化合物の添加によっ
て低温での崩壊性を改善したものである。しかし、この
発明による鋳型材料には、臭素含有有機化合物そのもの
が低温度(300〜40000)で分解し、その分解生
成物がャニとなって金型に附着堆積するため、シェル中
子の離型を困難にしたり、中子セットの寸法をくるわせ
るという欠点がある。また、添加物として塩化亜鉛を用
いたコーテッドサンドの組成物も提案されているが、こ
れには、その添加物中の塩素が強力な酸化作用を有する
ため金型を腐食させ易い欠点がある。本発明は、従来に
おける上記のような問題に対処するもので、コーテツド
サンドの崩壊剤として臭化亜鉛等の臭素化無機化合物を
用いる。
To address this situation, for example, there is an invention related to "shell mold mold material for casting light alloy" disclosed in Japanese Patent Application Laid-Open No. 57-149043. This is based on 100 parts by weight of foundry sand, 0.3 to 7 parts by weight of phenolic resin, and 0.001 to 7 parts by weight of Br-containing organic compound that splits Br or Br compounds by heating.
This method is characterized by coating the foundry sand with a composition consisting of 7 parts by weight, and has improved disintegration properties at low temperatures by adding a bromine-containing organic compound. However, in the mold material according to the present invention, the bromine-containing organic compound itself decomposes at low temperatures (300 to 40,000 ℃), and the decomposition products become sticky and deposit on the mold, so the shell core cannot be separated. There are disadvantages in that it makes molding difficult and the dimensions of the core set vary. A coated sand composition using zinc chloride as an additive has also been proposed, but this has the disadvantage that the chlorine in the additive has a strong oxidizing effect and tends to corrode the mold. The present invention addresses the above-mentioned conventional problems and uses a brominated inorganic compound such as zinc bromide as a disintegrant for coated sand.

これにより、低温での崩壊性がよく、しかもヤニの発生
や金型の腐食等を来たさない軽合金鋳物用として通した
コーテッドサンドの組成物を実現することを目的とする
。即ち、本発明に係るコーテツドサンドの組成物は、珪
砂等の耐火物粒子10碇部‘こ対してフェノール樹脂1
〜3部、臭化亜鉛等の臭素化無機化合物の少なくとも一
種を0.01〜1.0部の割合で添加混合してなること
を特徴とする。
The purpose of this is to realize a coated sand composition that has good disintegration properties at low temperatures and is suitable for use in light alloy castings without causing tar generation or corrosion of molds. That is, the coated sand composition according to the present invention contains 1 part of phenolic resin for every 10 parts of refractory particles such as silica sand.
~3 parts, and at least one kind of brominated inorganic compound such as zinc bromide is added and mixed in a ratio of 0.01 to 1.0 parts.

このような組成によれば、低温での崩壊性がよく、しか
もャニの発生や金型の腐食等を来たさない軽合金鋳物用
として適したコーテッドサンドを得ることができる。尚
、上記臭素化無機化合物は、0.01部より少ないと崩
壊性改良の効果がなく、1.0部より多いと強度の低下
が大きく実用上問題がある。好ましくは、0.05〜0
.5部である。次に実施例に基づいて本発明を説明する
With such a composition, it is possible to obtain a coated sand that has good disintegrability at low temperatures and is suitable for light alloy castings, which does not cause mold formation or mold corrosion. It should be noted that if the amount of the brominated inorganic compound is less than 0.01 part, there is no effect of improving the disintegration property, and if it is more than 1.0 part, the strength will be greatly reduced, which is a practical problem. Preferably 0.05-0
.. There are 5 parts. Next, the present invention will be explained based on examples.

実施例 1 実験用スピードマラー中に、150℃に加熱した*珪砂
10k9を入れ、固形ノボラック型フェノール樹脂を2
00タ添加して、4頂砂混練した後へキサメチレンテト
ラミン30夕と水150肌とからなる硬化水を添加し、
然る後、下記量の臭化亜鉛と水50のととらなる崩壊剤
を添加した。
Example 1 In an experimental speed maller, 10k9*silica sand heated to 150°C was placed, and 2 kg of solid novolac type phenolic resin was added.
After adding 0.00 g of sand and kneading 4 top sand, hardened water consisting of 30 g of hexamethylenetetramine and 150 g of water was added,
Thereafter, a disintegrant consisting of the following amounts of zinc bromide and 50 parts water was added.

そして、塊状物が解かれた後、ステアリン酸カルシウム
10夕を添加し、その1の酸・後に筋分け、冷却し、コ
ーテッドサンドを得た。このようにして得られたコーテ
ッドサンドは、臭化亜鉛の添加料に応じて第1表に記す
ような性能を示した。
After the lumps were loosened, 10 pieces of calcium stearate were added, and after the first acid, the mixture was divided into stripes and cooled to obtain coated sand. The coated sand thus obtained exhibited the properties listed in Table 1, depending on the zinc bromide additive.

満、比較例として、添加物なしの場合(比較例1)、臭
素含有有機化合物を珪砂に対して0.2%添加した場合
(比較例2、3)、及び塩素含有無機化合物を同じく0
.2%添加した場合(比較例4、5)の結果を同時に示
す。
As comparative examples, there are cases in which no additives are used (Comparative Example 1), cases in which 0.2% of bromine-containing organic compounds are added to silica sand (Comparative Examples 2 and 3), and cases in which 0.2% of bromine-containing inorganic compounds are added to silica sand.
.. The results for the cases where 2% was added (Comparative Examples 4 and 5) are shown at the same time.

第1表 その結果、臭化亜鉛を用いた場合、崩壊性が著しく向上
され、しかも、臭素含有有機化合物を添加した場合のよ
うな多量のャニ発生がなく、また塩素含有無機化合物よ
り金型の錆が軽微であることが判明した。
Table 1 As a result, when zinc bromide was used, the disintegration properties were significantly improved, and there was no generation of large amounts of gunk, unlike when bromine-containing organic compounds were added, and mold molding was better than that of chlorine-containing inorganic compounds. It was found that the rust was slight.

尚、第1表中、各項目の測定は各々下記のような試験法
又は測定法によって行った。
In addition, each item in Table 1 was measured by the following test method or measurement method.

融着点:JACT試験法C−1 抗折力:1′4″×1″×2″のテストピース(金型温
度250℃で6頂砂間焼成したもの)の両端を支持し、
その中央に荷重を加えてテストピースが折れたときの荷
重を、テストピースの断面積で除したときの値 ペンド:JACT試験法SM−3 崩壊性:図面に示す如き円筒状金型A(700×70)
、下型B(平板中央に150×20の丸陣をセットした
もの)にテスト用中子C(500×50)をセットして
、700q○のアルミニウムDを注湯する。
Fusion point: JACT test method C-1 Transverse rupture strength: Supporting both ends of a 1'4" x 1" x 2" test piece (fired between 6 tops of sand at a mold temperature of 250°C),
Value obtained by dividing the load when the test piece breaks by applying a load to its center by the cross-sectional area of the test piece Pend: JACT test method SM-3 Collapse property: Cylindrical mold A (700 ×70)
, Test core C (500 x 50) is set in lower mold B (150 x 20 circles set in the center of the flat plate), and 700q○ of aluminum D is poured into it.

その後30分放冷した後、金型枠からアルミニウム鋳物
を取り出し、これをエアー圧3kg′流のエアーハンマ
ーで9硯砂間打撃し、その際150の穴から出た崩壊物
の重量を測定して下記の式により求めた。
After cooling for 30 minutes, the aluminum casting was taken out from the mold frame and hit with an air hammer at 3 kg' of air pressure through 9 inkstone sands, and the weight of the collapsed material that came out of the 150 holes was measured. It was calculated using the following formula.

(崩壊物の重量/150)×100 ャニ発生量:上記抗折力の測定で用いたテストピース2
0夕を既知重量のアルミ箔で1重に包み、これを700
00の温度に設定された電気炉の中に入れて、9分間加
熱した放冷後、** アルミ箔に附着たヤニの量を
秤量し、これをャニ発生量とした。
(Weight of collapsible material/150) x 100 Amount of crab generated: Test piece 2 used in the above transverse rupture strength measurement
Wrap the aluminum foil in a single layer of aluminum foil of known weight, and add 700
The aluminum foil was placed in an electric furnace set at a temperature of 0.00, heated for 9 minutes, and left to cool.**The amount of tar adhering to the aluminum foil was weighed, and this was taken as the amount of tar generated.

金型の錆:上記崩壊性試験の下型Bを大気中に24時間
放置した後、中央部の普通鉄丸樺(150)の表面を倍
率3M音のルーペで観察し、鈴の発生度をみた。
Mold rust: After leaving the lower mold B of the above disintegration test in the air for 24 hours, the surface of the ordinary iron round birch (150) in the center was observed with a loupe with a magnification of 3M, and the degree of occurrence of bells was determined. saw.

実施例 ロ 臭化亜鉛以外の臭素化無機化合物を崩壊剤として添加し
た結果、第2表に示すような性能のコーテッドサンドが
得られた。
Example As a result of adding a brominated inorganic compound other than zinc brobromide as a disintegrant, coated sand with the performance shown in Table 2 was obtained.

ここで、臭素化無機化合物の珪砂に対する割合は0.2
%であり、またコーテツドサンドの製造方法及び効果の
測定方法は、実施例1と同じである。尚、第2表中には
、実施例1の所で述べた臭化亜鉛(珪砂に対する割合が
0.2%のもの)を用いた場合のコーテツドサンドの性
能を比較のため再記してある。第2表 この結果、臭化カルシウムが臭化亜鉛と同様に崩壊性が
優れ、且つャニ、錆の発生量が少ないことが判明した。
Here, the ratio of brominated inorganic compound to silica sand is 0.2
%, and the method for producing the coated sand and the method for measuring the effect are the same as in Example 1. In Table 2, the performance of coated sand using zinc bromide (0.2% of silica sand) as described in Example 1 is rewritten for comparison. . Table 2 As a result, it was found that calcium bromide, like zinc bromide, had excellent disintegration properties, and also produced less gunk and rust.

しかし、臭化亜鉛或いは臭化カルシウムに比較すると、
臭化アンモニウム及び臭化アルミニウムを用いた場合は
、錆の発生が多いこと、また臭化カリウム及び臭化ナト
リウムを用いた場合は、崩壊性が低いことなどがわかっ
た。以上のように、本発明によれば、低温での崩壊性が
良く、しかもャニの発生や金属の腐食が少なく、従って
エンジンのシリンダヘッド等の軽合金鋳物用として最適
のコーテッドサンドの組成物が得られる。
However, compared to zinc bromide or calcium bromide,
It was found that rust occurred frequently when ammonium bromide and aluminum bromide were used, and that disintegration was low when potassium bromide and sodium bromide were used. As described above, according to the present invention, the coated sand composition has good disintegration properties at low temperatures, and has little generation of mold and metal corrosion, and is therefore optimal for use in light alloy castings such as engine cylinder heads. is obtained.

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

図面は、崩壊性の確認に使用した装置の概略図である。 The drawing is a schematic diagram of the apparatus used to confirm collapsibility.

Claims (1)

【特許請求の範囲】 1 珪砂等の耐火物粒子100重量部に対し、フエノー
ル樹脂1〜3重量部、臭素化無機化合物0.01〜1.
0重量部の割合で混合してなることを特徴とする軽合金
鋳物用コーテツドサンド組成物。 2 臭素化無機化合物が臭化亜鉛であることを特徴とす
る特許請求の範囲第1項記載の軽合金鋳物用コーテツド
サンド組成物。
[Claims] 1. 1 to 3 parts by weight of a phenol resin and 0.01 to 1.0 parts by weight of a brominated inorganic compound per 100 parts by weight of refractory particles such as silica sand.
A coated sand composition for light alloy casting, characterized in that it is mixed in a proportion of 0 parts by weight. 2. The coated sand composition for light alloy casting according to claim 1, wherein the brominated inorganic compound is zinc bromide.
JP4383483A 1983-03-15 1983-03-15 Coated sand composition for light alloy casting Expired JPS6015417B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4383483A JPS6015417B2 (en) 1983-03-15 1983-03-15 Coated sand composition for light alloy casting

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4383483A JPS6015417B2 (en) 1983-03-15 1983-03-15 Coated sand composition for light alloy casting

Publications (2)

Publication Number Publication Date
JPS59189030A JPS59189030A (en) 1984-10-26
JPS6015417B2 true JPS6015417B2 (en) 1985-04-19

Family

ID=12674774

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4383483A Expired JPS6015417B2 (en) 1983-03-15 1983-03-15 Coated sand composition for light alloy casting

Country Status (1)

Country Link
JP (1) JPS6015417B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2504638B2 (en) * 1990-07-05 1996-06-05 花王株式会社 Curable mold manufacturing additive and method for manufacturing mold
DE69130141T2 (en) * 1990-07-05 1999-02-25 Kao Corp., Tokio/Tokyo Process for the production of casting molds
US5646199A (en) * 1991-07-22 1997-07-08 Kao Corporation Composition for mold

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5588452U (en) * 1978-12-15 1980-06-18
JPS58173227A (en) * 1982-04-01 1983-10-12 Kazuhiko Kono Key for manhole cover

Also Published As

Publication number Publication date
JPS59189030A (en) 1984-10-26

Similar Documents

Publication Publication Date Title
JP4610679B2 (en) Manufacturing procedures for ferrules for molds, other feeding heads and feeding elements, and compositions for the production of said ferrules and elements
US4767800A (en) Exothermic compositions
US6372032B1 (en) Foundry exothermic assembly
JP2013514179A (en) Casting sand mold and / or core manufacturing method and binder composition
US4877078A (en) Pattern for use in lost pattern foundry process
US5180759A (en) Exothermic compositions
JPS6015417B2 (en) Coated sand composition for light alloy casting
US4131476A (en) Additive for green molding sand
US3216078A (en) Process for casting steel and compositions of matter for use therein
US4636262A (en) Additive for green molding sand
CN109641261B (en) Foundry coating composition for non-permanent molds or cores for iron and steel casting
US2380201A (en) Manufacture of castings
US1888441A (en) Mold part
JPS61245938A (en) Compound for casting mold
US3110943A (en) Production of metal ingots, castings and the like
JP4714932B2 (en) Additive for disappearance model
JP3170870B2 (en) Sand core manufacturing method
JPS6039450B2 (en) Resin-coated sand grains for molding
US1919939A (en) Casting freely oxidizable metal
SU265381A1 (en) MIXTURE FOR FORMS AND ROD CASTING
RU2238168C1 (en) Additive for molding sands
JPS60108138A (en) Mold composition for casting
US1572382A (en) Metallic alloy
JP2001286977A (en) Mold and method of manufacturing mold
JPS62244546A (en) Coating agent for chilling cast steel castings