JPS6124097B2 - - Google Patents
Info
- Publication number
- JPS6124097B2 JPS6124097B2 JP7673780A JP7673780A JPS6124097B2 JP S6124097 B2 JPS6124097 B2 JP S6124097B2 JP 7673780 A JP7673780 A JP 7673780A JP 7673780 A JP7673780 A JP 7673780A JP S6124097 B2 JPS6124097 B2 JP S6124097B2
- Authority
- JP
- Japan
- Prior art keywords
- mold
- coating
- weight
- molds
- 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.)
- Expired
Links
- 238000000576 coating method Methods 0.000 claims description 34
- 239000011248 coating agent Substances 0.000 claims description 30
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 23
- 239000011230 binding agent Substances 0.000 claims description 14
- 239000000463 material Substances 0.000 claims description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 8
- 239000011347 resin Substances 0.000 claims description 8
- 229920005989 resin Polymers 0.000 claims description 8
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 claims description 6
- 239000010410 layer Substances 0.000 claims description 6
- 239000000377 silicon dioxide Substances 0.000 claims description 6
- RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 claims description 5
- 239000003085 diluting agent Substances 0.000 claims description 5
- 239000011247 coating layer Substances 0.000 claims description 4
- 239000002244 precipitate Substances 0.000 claims 1
- 239000004576 sand Substances 0.000 description 11
- 238000005266 casting Methods 0.000 description 9
- 230000000694 effects Effects 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- 239000002245 particle Substances 0.000 description 7
- 235000019441 ethanol Nutrition 0.000 description 5
- 239000005011 phenolic resin Substances 0.000 description 5
- 230000035515 penetration Effects 0.000 description 4
- 230000035699 permeability Effects 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 229910001208 Crucible steel Inorganic materials 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000007849 furan resin Substances 0.000 description 3
- 230000000149 penetrating effect Effects 0.000 description 3
- 238000004062 sedimentation Methods 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- -1 ascent Chemical compound 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 230000000573 anti-seizure effect Effects 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229910052596 spinel Inorganic materials 0.000 description 1
- 239000011029 spinel Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
Description
本発明は焼着防止効果の大なる塗型に関するも
のである。
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同志の空隙中に浸入し、型
ばらしの際に砂落ちが悪くなるのを防止するこ
と、および良好な鋳肌を有する鋳造金属を得るこ
とを目的として塗型が塗布される。従来の塗型で
は、鋳鋼用には、粘結剤としてフエノール樹脂や
コロフオニウム(天然ロジン)が、また溶剤とし
てアルコールが通常使用されており、これらアル
コール系塗型は鋳型表面に刷毛塗りやスプレー塗
布される。
従来の塗型に粘結剤として使用されているフエ
ノール樹脂やコロフオニウムは、塗布厚さ1.0mm
付近までとかなり厚く塗布することができ、塗布
後の塗型の常温強度を確保する点では優れている
が、これらの樹脂は耐熱性が不十分なため、溶融
金属、特に鋳鋼を鋳造した際には塗型膜に亀裂が
生じ溶湯が浸入しやすく、また従来の塗型は鋳型
への浸透性が小さいため塗型による砂粒子間隙の
目つぶし効果が小さく、上記のように塗型層を通
過した溶湯は鋳型の砂粒子間隙に容易に浸入する
ので、焼着防止効果が不十分であるという欠点が
あつた。
本発明者等は上記の溶湯による焼着に対して十
分な焼着防止効果を示す塗型を提供すべく研究を
重ねた結果、焼着、特に浸透性焼着を防止するに
は鋳型表面の砂粒子間隙を埋めることが最も必要
と考え、浸透性の優れた焼結層を形成しやすい塗
型を下塗りとし、その上にこの塗型焼結層が鋳物
表面から分離しやすいように、従来から使用され
ている有機樹脂を含む塗型を塗布し、それぞれ役
目を異にする塗型を二重塗りする本発明に到達し
たものである。本発明における下塗り塗型として
は、耐熱性が優れた高温強度の高いシリカ分を形
成するエチル・シリケート加水分解液を粘結剤と
して用い、またこの下塗り塗型によつて鋳型の砂
粒子間隙が充填されやすいよう、即ち、塗型が鋳
型表面から2mm以上、浸透するように、塗型にお
ける基材と、粘結剤を含む希釈剤との割合を基材
50〜90重量%、希釈材50〜10重量%とするもので
ある。この下塗り塗型の浸透深さは、種々検討し
た結果、最低2mm以上が必要と判断されたが、塗
型の基材が多くなるほど塗型の浸透深さは浅くな
るので90重量%までに抑える必要があり、一方、
基材の割合が低下すると浸透性は向上するが、塗
布時の作業性、特に刷毛塗り時の塗型の伸び性が
低下するので基材の下限を50重量%とするもので
ある。基材としてはジルコン粉末、アルミナ
(Al2O3)、スピネル(MgO・Al2O3)、酸化クロム
(Cr2O3)などが用いられる。希釈剤中の粘結剤と
しては上記の如くシリカ分を形成するエチル・シ
リケート加水分解液を用い、また塗型の懸濁性を
保持し、沈降性を低減するためにコロフオニウム
(天然ロジン)を添加する。エチルシリケート加
水分解液のゲル化防止、塗型の沈降防止および注
湯時のガス欠陥の防止の観点から、シリカ分0.15
〜0.75重量%、コロフオニウム0.5〜2.5重量%
で、シリカ分:コロフオニウム=3:10のものが
特によいことが判明した。溶剤としてはエチルア
ルコール、イソプロピルアルコール、ブタノール
等アルコール類を主溶剤として用い、これに助溶
剤として酢酸エチル、酢酸ブチル、アセント、ト
ルエンなどを添加使用することができる。
上塗り塗型は通常、用いられる塗型を用いれば
よいが、主湯時に焼結した下塗り塗型が鋳物から
分離しやすいように下塗り塗型に比較して鋳型表
面に厚く塗布できるものがよく、粘結剤としてフ
エノール樹脂、コロフオニウム等の有機樹脂粘結
剤を(上記した下塗り塗型の粘結剤に含まれるエ
チルシリケート加水分解液は含まれない)を、溶
剤としてアルコールを用いたものが適しており、
塗型の保存性(懸濁性)の確保のためにベントナ
イト等を添加することもできる。コロフオニウム
は塗型基材の粘結作用と沈降防止作用の両機能を
有し、基材がゲル化しやすい下塗り塗型では沈降
防止作用を、またゲル化しやすいものが含まれて
いない上塗り塗型では粘結作用を利用しているも
のである。
本発明の鋳型用塗型は、鉄系および非鉄系金属
を鋳造する際に発生ししやすい浸透性焼着の防止
に有効であり、鋳型としてはベントナイトを粘結
剤とする生型、フエノール樹脂を粘結剤とするシ
エル型、フエノール樹脂、ポリイソシアネート樹
脂を粘結剤とするコールド・ボツクス、その他リ
ノキユア型、ペツブセツト型など有機樹脂を粘結
剤とした鋳型等種々のものに適しているが、特に
砂の再生回収が容易なため近年、鋳鋼用鋳型とし
ても広く導入かれてきているフラン鋳型に適した
塗型である。
添付の図面に、本発明の塗型を塗布した鋳型の
断面を示す。鋳型は砂粒子1で構成され、下塗り
塗型2は浸透性が優れているため、上塗り塗型3
層の4倍(2mm以上)程度、砂粒子間隙に浸入
し、砂粒子間隙を充填している。
例
フラン樹脂鋳型(珪砂100%に、フラン樹脂1.0
%、触媒としてパラトルエンスルホン酸をフラン
樹脂に対して40%添加)に、下塗り塗型として第
1表に示す例1、例2の塗型を浸透深さ各々約
2.5mm、4.0mmで塗布し、着火乾燥した。下塗り塗
型の乾燥法はどのようなものでもよいが、この着
火乾燥によれば、上塗り塗型が直ちに塗布できる
ので塗型塗布工程が短縮され、また着火乾燥した
残熱で上塗り塗型の乾燥時間が短縮される。
The present invention relates to a coating mold that has a large anti-seizing effect. Conventionally, for casting molds, it has been necessary to prevent molten metal from penetrating into the voids between the sand particles that form the mold, preventing sand from falling off when the mold is disassembled, and to maintain a good casting surface. A mold is applied with the aim of obtaining a cast metal with a In conventional coating molds for cast steel, phenolic resin or collophonium (natural rosin) is usually used as a binder, and alcohol is used as a solvent, and these alcohol-based coatings are applied by brushing or spraying onto the mold surface. be done. Phenol resin and colophonium, which are used as binders in conventional coating molds, have a coating thickness of 1.0 mm.
These resins can be applied fairly thickly, up to almost 300 ml, and are excellent in ensuring the strength of the coated mold at room temperature after application. However, these resins have insufficient heat resistance, so when casting molten metal, especially cast steel, Cracks occur in the coating film, making it easy for molten metal to infiltrate, and because conventional coatings have low permeability into the mold, the effect of closing the gaps between sand particles by the coating is small, and as shown above, the molten metal can easily penetrate through the coating layer. Since the molten metal easily penetrates into the gaps between the sand particles in the mold, the anti-seizing effect is insufficient. The present inventors have conducted extensive research in order to provide a coating mold that has a sufficient anti-seizing effect against the above-mentioned molten metal-induced seizing. Considering that it is most necessary to fill the gaps between sand particles, we use a coating that is easy to form a sintered layer with excellent permeability as an undercoat, and apply conventional coatings on top of that to make it easier for the sintered layer to separate from the casting surface. The present invention has been achieved by applying a coating mold containing an organic resin, which has been used since then, and applying a double coat of coating molds each having a different role. The undercoat mold in the present invention uses as a binder an ethyl silicate hydrolyzed solution that forms a silica component with excellent heat resistance and high temperature strength. The ratio of the base material and the diluent containing the binder in the coating mold is adjusted so that it is easy to fill, that is, the coating penetrates 2 mm or more from the mold surface.
The content is 50 to 90% by weight, and the diluent is 50 to 10% by weight. After various studies, it was determined that the penetration depth of this undercoating mold should be at least 2 mm or more, but the more base materials there are in the coating mold, the shallower the penetration depth of the coating mold becomes, so it should be kept to 90% by weight. On the other hand, there is a need
As the percentage of the base material decreases, the permeability improves, but the workability during application, especially the elongation of the coating mold during brush application, decreases, so the lower limit of the base material is set at 50% by weight. As the base material, zircon powder, alumina (Al 2 O 3 ), spinel (MgO.Al 2 O 3 ), chromium oxide (Cr 2 O 3 ), etc. are used. As the binder in the diluent, an ethyl silicate hydrolyzate that forms a silica component is used as described above, and colophonium (natural rosin) is used to maintain the suspendability of the coating mold and reduce sedimentation. Added. Silica content: 0.15 from the viewpoint of preventing gelation of the ethyl silicate hydrolyzed solution, prevention of sedimentation of the coating mold, and prevention of gas defects during pouring.
~0.75 wt%, Corophonium 0.5-2.5 wt%
It was found that a material with a silica content: colophonium ratio of 3:10 was particularly good. As the solvent, alcohols such as ethyl alcohol, isopropyl alcohol, and butanol are used as the main solvent, and to this, ethyl acetate, butyl acetate, ascent, toluene, etc. can be added as a co-solvent. For the topcoat mold, it is sufficient to use the mold that is normally used, but it is better to use one that can be applied thicker to the mold surface compared to the undercoat mold so that the undercoat mold sintered during the main melting can be easily separated from the casting. It is suitable to use an organic resin binder such as phenol resin or colophonium as a binder (the ethyl silicate hydrolyzate contained in the above-mentioned undercoat type binder is not included) and alcohol as a solvent. and
Bentonite or the like may also be added to ensure the preservability (suspendability) of the coating mold. Corophonium has both a caking effect and an anti-sedimentation effect on the coating base material, and it acts as an anti-settling effect in the undercoat type where the base material tends to gel, and in the top coat type that does not contain materials that easily gel. It utilizes caking effect. The coating mold for molds of the present invention is effective in preventing penetrating seizure that tends to occur when casting ferrous and non-ferrous metals, and the molds can be green molds with bentonite as a binder, phenolic resins, etc. It is suitable for a variety of molds, including shell molds that use organic resin as a binder, cold boxes that use phenol resins and polyisocyanate resins as a binder, and molds that use organic resins as a binder, such as linokure molds and pebble molds. In particular, it is a coating mold suitable for flan molds, which have been widely introduced as molds for casting steel in recent years because sand can be easily recycled and recovered. The accompanying drawing shows a cross-section of a mold coated with the coating of the invention. The mold is composed of sand particles 1, and the undercoat mold 2 has excellent permeability, so the topcoat mold 3
It penetrates into the gaps between sand particles to a depth of about four times the layer (more than 2 mm) and fills the gaps between sand particles. Example: Furan resin mold (100% silica sand, 1.0 furan resin)
%, para-toluenesulfonic acid was added as a catalyst to the furan resin at a rate of 40%), and the coating molds of Examples 1 and 2 shown in Table 1 were applied as undercoat molds to a penetration depth of approximately
It was applied at 2.5mm and 4.0mm and dried by ignition. Any method can be used to dry the undercoat mold, but with this ignition drying method, the topcoat mold can be applied immediately, which shortens the coating process, and the remaining heat from ignition drying can dry the topcoat mold. Time is reduced.
【表】
次いで上塗り塗型として第2表に示す塗型を
0.3〜0.5mm塗布して、鋳鋼(SC 42)を1570℃で
鋳込んだ。[Table] Next, use the coating type shown in Table 2 as the top coating type.
Cast steel (SC 42) was cast at 1570°C with a coating of 0.3-0.5mm.
【表】
その結果、鋳込重量1000Kgまでの鋳物では、例
1、例2とも浸透性の焼着は全く発生せず、しか
ほ砂の型ばらしも極めて良好であつた。鋳込重量
が1000Kgを超える場合は、例2のように浸透深さ
を4mm程度まで深くする方が、焼着防止効果が安
定していた。[Table] As a result, in both Examples 1 and 2, in the case of castings with a casting weight of up to 1000 kg, no penetrating seizure occurred at all, and the mold release of the sand was very good. When the cast weight exceeds 1000 kg, increasing the penetration depth to about 4 mm as in Example 2 resulted in a more stable anti-seizure effect.
添付図面は本発明の塗布した鋳型の断面を示
す。
The accompanying drawing shows a cross-section of a coated mold according to the invention.
Claims (1)
重量%とからなり、該希釈剤が粘結剤としてシリ
カ分を0.15〜0.75重量%析出するエチルシリケー
ト加水分解液、コロフオニウム0.5〜2.5重量%、
及び残部アルコールからなる、アルコール系塗型
を鋳型表面から浸透させて形成した下塗り塗型
層、その上に第2層として、有機樹脂粘結剤を含
み、エチルシリケート加水分解液を含まないアル
コール系塗型を塗布した上塗り塗型層、の2種類
の塗型層からなる塗型。1 The first layer contains 50-90% by weight of the base material and 50-10% by weight of the diluent.
an ethyl silicate hydrolyzate in which the diluent acts as a binder and precipitates 0.15 to 0.75% by weight of silica; 0.5 to 2.5% by weight of colophonium;
and the remainder alcohol, an undercoat layer formed by permeating an alcohol-based coating mold from the mold surface, and on top of that, a second layer containing an alcohol-based coating containing an organic resin binder and not containing an ethyl silicate hydrolyzate. A coating mold that consists of two types of coating layers: a top coat coating layer and a coating coating layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7673780A JPS574353A (en) | 1980-06-09 | 1980-06-09 | Mold coating material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7673780A JPS574353A (en) | 1980-06-09 | 1980-06-09 | Mold coating material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS574353A JPS574353A (en) | 1982-01-09 |
JPS6124097B2 true JPS6124097B2 (en) | 1986-06-09 |
Family
ID=13613899
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7673780A Granted JPS574353A (en) | 1980-06-09 | 1980-06-09 | Mold coating material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS574353A (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60114286A (en) * | 1983-11-26 | 1985-06-20 | 株式会社平和 | Chicket publication machine of pinball machine |
JPS62104648A (en) * | 1985-10-30 | 1987-05-15 | Sadaji Nagabori | Production of sand mold for casting |
JPS62296931A (en) * | 1986-06-18 | 1987-12-24 | Ryobi Ltd | Production of breakable core for high pressure casting |
KR101199857B1 (en) | 2011-01-20 | 2012-11-09 | 주식회사 성일터빈 | A Mold and A Mold Manufacturing Method By Dual-Coating Process |
KR101287146B1 (en) * | 2011-01-20 | 2013-07-17 | 현대메티아 주식회사 | A Bead, A Mold, A Product manufactured by A Mold, A Bead Manufacturing Method and A Mold Manufacturing Method by Dual-coating Process |
-
1980
- 1980-06-09 JP JP7673780A patent/JPS574353A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS574353A (en) | 1982-01-09 |
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