JPS5843169B2 - Resin coated sand - Google Patents
Resin coated sandInfo
- Publication number
- JPS5843169B2 JPS5843169B2 JP12919575A JP12919575A JPS5843169B2 JP S5843169 B2 JPS5843169 B2 JP S5843169B2 JP 12919575 A JP12919575 A JP 12919575A JP 12919575 A JP12919575 A JP 12919575A JP S5843169 B2 JPS5843169 B2 JP S5843169B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- sand
- coated
- shell
- coated sand
- 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
- 229920005989 resin Polymers 0.000 title claims description 58
- 239000011347 resin Substances 0.000 title claims description 58
- 239000004576 sand Substances 0.000 title claims description 44
- 229920002554 vinyl polymer Polymers 0.000 claims description 12
- 239000002245 particle Substances 0.000 claims description 11
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 11
- 229920001187 thermosetting polymer Polymers 0.000 claims description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 49
- 238000000034 method Methods 0.000 description 18
- 238000005266 casting Methods 0.000 description 15
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- 229910000838 Al alloy Inorganic materials 0.000 description 6
- 229910045601 alloy Inorganic materials 0.000 description 6
- 239000000956 alloy Substances 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000010112 shell-mould casting Methods 0.000 description 2
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- 229910001208 Crucible steel Inorganic materials 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 150000001241 acetals 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
- 230000000694 effects Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000005350 fused silica glass Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 1
- 239000004312 hexamethylene tetramine Substances 0.000 description 1
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 1
- 238000005495 investment casting Methods 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052609 olivine Inorganic materials 0.000 description 1
- 239000010450 olivine Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 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
Landscapes
- Mold Materials And Core Materials (AREA)
Description
【発明の詳細な説明】
本発明は、レジンコーテツドサンドに係わり、耐火物粒
子の表面をビニル系樹脂、熱硬化性樹脂の順に二層に被
覆し、鋳込み後の崩壊性のすぐれたシェルモールド法用
のレジンコーテツドサンドに関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to resin-coated sand, in which the surface of refractory particles is coated with two layers of vinyl resin and thermosetting resin in that order, thereby forming a shell mold with excellent disintegration properties after casting. This relates to resin-coated sand for legal use.
シェルモールド法は、第二次犬戦中にドイツで発明され
た一種の精密鋳造法であるが、当初、造型材料として砂
と粉末レジンの混合物が使用されていた。The shell molding method is a type of precision casting method invented in Germany during the Second War, and initially a mixture of sand and powdered resin was used as the molding material.
この混合物は、砂とレジンの比重が異なるため、圧縮空
気を使って該混合物をコアボックスの中に吹き込むと両
者が分離し、特にコアボックスと接する中子表面部のレ
ジン濃度が異常に上昇するため、コアボックスからの中
子の離型が容易でないばかりでなく、鋳造品にガス欠陥
の発生を見ることもしばしばあった。In this mixture, sand and resin have different specific gravity, so when the mixture is blown into the core box using compressed air, the two will separate and the resin concentration will increase abnormally, especially on the surface of the core that contacts the core box. Therefore, not only was it not easy to release the core from the core box, but gas defects often occurred in the cast product.
これらの欠陥を取り除いたものが、砂粒子の表面をレジ
ンにより被覆したレジンコーテツドサンドである。Resin-coated sand, in which the surface of sand particles is coated with resin, has these defects removed.
レジンコーテツドサンドは、レジン被覆前の耐火物粒子
に匹敵ないしはこれを凌駕する流動性を有し、中空中子
の成型並びに薄肉のシェルモールドないしはシェル中子
を容易に成型することができる。Resin-coated sand has fluidity comparable to or exceeding that of refractory particles before being coated with resin, and can be easily molded into hollow cores and thin shell molds or shell cores.
レジンコーテツドサンド製のシェルモールド並びにシェ
ル中子は、砂粉末しジン混合物製のシェルモールド並び
にシェル中子に比べて、強度が著しく強いので、砂に対
するレジンの添加比率を重量比でほぼ半減させることが
できる。Shell molds and shell cores made of resin-coated sand are significantly stronger than shell molds and shell cores made of sand powder and resin mixtures, so the ratio of resin to sand added can be reduced by almost half by weight. be able to.
レジンコーテツドサンド製のシェルモールドまたはシェ
ル中子に銅合金、鋳鉄、鋼など融点の高い金属または合
金を鋳込むと、レジンが熱分解し、続いて燃焼するため
、シェルモールドまたはシェル中子は崩壊性が非常にす
ぐれている。If a metal or alloy with a high melting point, such as copper alloy, cast iron, or steel, is cast into a shell mold or shell core made of resin-coated sand, the resin will thermally decompose and subsequently burn, causing the shell mold or shell core to It has excellent disintegration properties.
しかし、シェルモールドまたはシェル中子を使ってアル
ミニウム合金など低融点の金属または合金を鋳造すると
レジンがほとんど熱分解せず燃焼もしないため、特に中
子の崩壊性が悪く、′砂焼き“などと称して中子を内蔵
する製品を500℃前後で数時間加熱する作業が一般的
に行なわれており、省力並びに省エネルギ′−を進める
うえでの隘路となっている。However, when casting low melting point metals or alloys such as aluminum alloys using shell molds or shell cores, the resin hardly thermally decomposes or burns, so the core has particularly poor collapsibility, resulting in problems such as 'sand firing'. It is common practice to heat products containing a core at around 500 DEG C. for several hours, which is a bottleneck in efforts to save labor and energy.
アルミニウム合金など融点の低い合金を鋳造する際のシ
ェルモールド、特にシェル中子の鋳込み後の崩壊性を改
善するために、種種の発明がなされている。Various inventions have been made to improve the collapsibility of shell molds, especially shell cores, after casting when casting alloys with low melting points such as aluminum alloys.
たとえば、過マンガン酸カリウムや硝酸カリウムなどの
無機塩類を助燃剤としてレジンコーテツドサンドに添加
する方法が提案されているが、上記助燃剤が粉末状であ
るため、シェルモールド並びにシェル中子の強度低下を
きたし、鋳込み後の崩壊性も前記の砂焼きを廃止すると
ころまで改善されるに至らない。For example, a method has been proposed in which inorganic salts such as potassium permanganate and potassium nitrate are added to resin-coated sand as combustion improvers, but since the combustion improvers are in powder form, the strength of the shell mold and shell core is reduced. However, the disintegration properties after casting have not been improved to the point where the sand baking process is abolished.
耐火物粒子に対するレジンの被覆量を減らし、逆に該レ
ジンに対するヘキサミンの添加量を増しても崩壊性が改
善されるといわれているが、この方法によっても砂焼き
を廃止することはできない。It is said that collapsibility can be improved by reducing the amount of resin coated on the refractory particles and conversely increasing the amount of hexamine added to the resin, but sand baking cannot be abolished even with this method.
本発明者らは、レジンコーテツドサンド製のシェル中子
を使ってアルミニウム合金などの低融点の金属または合
金を鋳造する際の鋳込み後の崩壊性を改善するため、種
種検討した結果、満足すべき新規なレジンコーテツドサ
ンドを得た。The present inventors investigated various methods to improve the disintegration after casting when casting low melting point metals or alloys such as aluminum alloys using a shell core made of resin coated sand, and as a result, they were satisfied. We obtained a new resin-coated sand.
本発明の目的は、通常のレジンコーテツドサンドに匹敵
する流動性を有し、シェルモールド成型後の強度は通常
のレジンコーテツドサンド製のシェルモールドより強く
、しかも、アルミニウム合金などの低融点の金属または
合金を鋳込んだ後の崩壊性のすぐれたレジンコーテツド
サンドを提供することにある。The object of the present invention is to have fluidity comparable to that of ordinary resin coated sand, have stronger strength after shell molding than ordinary shell molds made of resin coated sand, and have low melting point materials such as aluminum alloys. An object of the present invention is to provide resin-coated sand with excellent collapsibility after casting metal or alloy.
本発明に係わるレジンコーテツドサンドは、耐火物粒子
の表面をまずビニル系樹脂により被覆し、その上を更に
熱硬化性樹脂によって被覆したことを特徴とする。The resin-coated sand according to the present invention is characterized in that the surface of the refractory particles is first coated with a vinyl resin, and then further coated with a thermosetting resin.
本発明に使用するビニル系樹脂は、ポリビニルアセテー
ト、ポリビニルアルコール、ポリビニルアセタール類、
ポリスチレンなどである。Vinyl resins used in the present invention include polyvinyl acetate, polyvinyl alcohol, polyvinyl acetals,
such as polystyrene.
本発明に使用する熱硬化性樹脂は、レジンコーテツドサ
ンドの製造に通常使われている熱硬化性樹脂ならばどれ
でもよく、特に制限はない。The thermosetting resin used in the present invention is not particularly limited and may be any thermosetting resin commonly used in the production of resin coated sand.
本発明に使用する耐火物粒子は、通常の鋳型用の耐火物
、たとえば、ケイ砂、オリビンサンド、クロマイトサン
ド、ジルコンサンド、溶融石英粒、アルミナ粒などであ
る。The refractory particles used in the present invention are ordinary refractories for molds, such as silica sand, olivine sand, chromite sand, zircon sand, fused silica grains, and alumina grains.
前記ビニル系樹脂による耐火物粒子の被覆は、通常のレ
ジンコーテツドサンドと同様、ホットプロセスによって
もセミホットプロセスによってもあるいはコールドプロ
セスによっても行なうことができる。The coating of the refractory particles with the vinyl resin can be carried out by a hot process, a semi-hot process, or a cold process, as in the case of ordinary resin-coated sand.
ビニル系樹脂の被覆量は、重量比で0.1〜3.0%、
好ましくは0.3〜1.5%である。The coating amount of vinyl resin is 0.1 to 3.0% by weight,
Preferably it is 0.3 to 1.5%.
被覆量の下限を重量比で0.1%としたのは、これを下
まわると折角被覆しても、鋳込み後の崩壊性を改善する
効果が認められないからである。The reason why the lower limit of the coating amount is set to 0.1% by weight is that if the coating amount is less than this, no effect of improving the collapsibility after casting will be observed even if the coating is applied at all costs.
被覆量の上限を重量比で3%としたのは、これ以上被覆
量を増しても材料費のみ上昇してそれに見合う崩壊性の
改善が期待されないばかりでなく、鋳造品にガス欠陥の
発生を見るに至るからである。The reason for setting the upper limit of the coating amount to 3% by weight is that increasing the coating amount beyond this will not only increase the material cost and not improve the collapsibility commensurately, but also cause gas defects to occur in the cast product. Because you will see it.
ビニル系樹脂により表面を被覆した耐火物粒子に対する
熱硬化樹脂による被覆は、通常のレジンコーテツドサン
ドと同様、ホットプロセスによっても、セミホットプロ
セスによっても、あるいはコールドプロセスによっても
行なうことができる。The refractory particles whose surfaces are coated with a vinyl resin can be coated with a thermosetting resin by a hot process, a semi-hot process, or a cold process, as in the case of ordinary resin-coated sand.
耐火物粒子の表面をまずビニル系樹脂によって被覆し、
その上を更に熱硬化性樹脂によって被覆した本発明のレ
ジンコーテツドサンドによるシェルモールド並びにシェ
ル中子の造型は、通常のレジンコーテツドサンドによる
場合と全く同様の方法で行なうことができる。The surface of the refractory particles is first coated with vinyl resin,
Molding of shell molds and shell cores using the resin-coated sand of the present invention, which is further coated with a thermosetting resin, can be carried out in exactly the same manner as when using ordinary resin-coated sand.
このようにして造型したシェルモールド並びにシェル中
子、特にシェル中子は、アルミニウム合金のように融点
の低い金属または合金を鋳込んでも、ビニル系樹脂が熱
分解して気化するため、崩壊性が非常にすぐれている。Shell molds and shell cores formed in this way, especially shell cores, are not easily disintegrated even when metals or alloys with low melting points such as aluminum alloys are cast, as the vinyl resin thermally decomposes and vaporizes. Very good.
以下好ましい実施例について詳述する。Preferred embodiments will be described in detail below.
実施例 1
ケイ砂100重量部の表面を1重量部のポリビニルアル
コールをもってコールドプロセスにより被覆し、溶剤を
完全に蒸発させた後、その表面を更に2.5重量部のフ
ェノールレジンをもってコールドプロセスにより被覆し
、溶剤を完全に蒸発させてレジンコーテツドサンドを製
造した。Example 1 The surface of 100 parts by weight of silica sand was coated with 1 part by weight of polyvinyl alcohol in a cold process, and after the solvent was completely evaporated, the surface was further coated with 2.5 parts by weight of phenol resin in a cold process. Then, the solvent was completely evaporated to produce resin coated sand.
該レジンコーテツドサンドによってシェルモールドの抗
折力試験片(o 10m1X 60mm)を成型し、同
試験片を中子1としてガス型に納め、該鋳型にアルミニ
ウム合金(AC2B)を鋳込んで第1図に示す鋳物2を
鋳造した。A shell mold transverse rupture strength test piece (o 10 m 1 x 60 mm) was molded using the resin coated sand, and the test piece was placed in a gas mold as core 1. Aluminum alloy (AC2B) was then cast into the mold. A casting 2 shown in the figure was cast.
該鋳物が常温に怜却した後、第2図に示す方法で中子の
崩壊性試験を行なった。After the casting had cooled to room temperature, a core disintegration test was conducted using the method shown in FIG.
すなわち、鋳物からの高さ450mmの位置より3に9
の重錘3を自由落下させ、衝撃により中子砂を落し、完
全に中子砂が除去されるまでの重錘3落下回数により崩
壊性の程度を表示した。In other words, from the height of 450 mm from the casting, 3 to 9
The weight 3 was allowed to fall freely, the core sand was dropped by impact, and the degree of collapsibility was expressed by the number of times the weight 3 was dropped until the core sand was completely removed.
レジンコーテツドサンドの製造法並びに得られた結果を
第1表に示す。The method for producing the resin coated sand and the results obtained are shown in Table 1.
実施例 2
前記実施例1では、ケイ砂100重量部の表面を1重量
部のポリビニルアルコールをもってコールドプロセスに
より被覆し、溶剤を完全に蒸発させた後、その表面を更
に2.5重量部のフェノールレジンをもってコールドプ
ロセスにより被覆し、溶剤を完全に蒸発させてレジンコ
ーテツドサンドを製造したが、本実施例2では、2層目
を1.5重量部のフェノールレジンをもってコールドプ
ロセスにより被覆し、溶剤を完全に蒸発させてレジンコ
ーテツドサンドを製造した。Example 2 In Example 1, the surface of 100 parts by weight of silica sand was coated with 1 part by weight of polyvinyl alcohol by a cold process, and after the solvent was completely evaporated, the surface was further coated with 2.5 parts by weight of phenol. Resin-coated sand was produced by coating with resin in a cold process and completely evaporating the solvent. In this Example 2, the second layer was coated with 1.5 parts by weight of phenol resin in a cold process, and the solvent was completely evaporated to produce resin coated sand.
該レジンコーテツドサンドについて実施例1と全く同様
の方法により崩壊性試験を行なった。A disintegration test was conducted on the resin coated sand in exactly the same manner as in Example 1.
レジンコーテツドサンドの製造法並びに得られた結果を
第2表に示す。The method of manufacturing the resin coated sand and the results obtained are shown in Table 2.
上述のように本発明のレジンコーテツドサンドは、耐火
物粒子の表面をまず熱分解温度の低いビニル系樹脂によ
り一様に被覆しているため、アルミニウム合金のような
溶融点の低い金属または合金と接してもビニル系樹脂が
容易に熱分解してすぐれた崩壊性を与え、鋳造作業後の
後処理を容易にすると共に、美麗な鋳肌の鋳物を得るこ
とができる等工業上の効果が多大である。As mentioned above, in the resin coated sand of the present invention, the surface of the refractory particles is first uniformly coated with a vinyl resin with a low thermal decomposition temperature. The vinyl resin easily thermally decomposes even when in contact with other materials, giving it excellent disintegrability, facilitating post-processing after casting work, and providing industrial benefits such as the ability to obtain castings with beautiful casting surfaces. It's a huge amount.
第1図は鋳造試験片を示し、第2図は崩壊性の試験方法
を示す図である。FIG. 1 shows a cast test piece, and FIG. 2 shows a collapsibility test method.
Claims (1)
、その上を更に熱硬化性樹脂によって被覆したことを特
徴とするレジンコーテツドサンド。1. A resin-coated sand characterized in that the surface of refractory particles is first coated with a vinyl resin, and then further coated with a thermosetting resin.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12919575A JPS5843169B2 (en) | 1975-10-29 | 1975-10-29 | Resin coated sand |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12919575A JPS5843169B2 (en) | 1975-10-29 | 1975-10-29 | Resin coated sand |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5253723A JPS5253723A (en) | 1977-04-30 |
| JPS5843169B2 true JPS5843169B2 (en) | 1983-09-26 |
Family
ID=15003483
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12919575A Expired JPS5843169B2 (en) | 1975-10-29 | 1975-10-29 | Resin coated sand |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5843169B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS588938B2 (en) * | 1980-01-12 | 1983-02-18 | マツダ株式会社 | Manufacturing method of resin-coated sand for molds |
-
1975
- 1975-10-29 JP JP12919575A patent/JPS5843169B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5253723A (en) | 1977-04-30 |
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