JPS588938B2 - Manufacturing method of resin-coated sand for molds - Google Patents
Manufacturing method of resin-coated sand for moldsInfo
- Publication number
- JPS588938B2 JPS588938B2 JP55002240A JP224080A JPS588938B2 JP S588938 B2 JPS588938 B2 JP S588938B2 JP 55002240 A JP55002240 A JP 55002240A JP 224080 A JP224080 A JP 224080A JP S588938 B2 JPS588938 B2 JP S588938B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- sand
- coated
- polyvinyl alcohol
- molds
- 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
Landscapes
- Mold Materials And Core Materials (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
【発明の詳細な説明】
本発明は、鋳造鋳型として使用する鋳物砂、とくに、表
面に樹脂を被覆した鋳型用樹脂被覆砂の製造法に関する
ものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing molding sand used as a casting mold, particularly resin-coated sand for molding whose surface is coated with a resin.
一般に、鋳物砂は、注湯前にあっては必要な強度を維持
し、鋳込後は崩壊性が良好なものが好ましい。Generally, foundry sand is preferably one that maintains the necessary strength before pouring and has good disintegration properties after pouring.
このため、従来、粘結剤としてフェノール樹脂等を用い
、砂の表面をフェノール樹脂等で被覆し、鋳込の際には
、必要な強度を維持しうるようにした鋳型用樹脂被覆砂
が提案されている。For this reason, resin-coated sand for molds has been proposed, which uses phenolic resin as a binder and coats the surface of the sand with phenolic resin to maintain the necessary strength during casting. has been done.
しかしながら、この種の樹脂被覆砂は、鋳込温度の高い
鋳鉄等の場合には、比較的良好な崩壊性を示すものの、
鋳込温度の低いアルミ等の鋳造の場合には、崩壊性が充
分でな《、鋳込後の鋳物の砂落し特に中子の排出に手間
取るといった問題があった。However, although this type of resin-coated sand shows relatively good disintegration properties when used with cast iron, etc., which has a high casting temperature,
When casting materials such as aluminum, which have a low casting temperature, there are problems in that the disintegrability is insufficient and it takes time to remove sand from the casting after casting, especially to eject the core.
かかる問題を解消するため、特公昭54−120229
号公報には、「フェノールホルムアルデヒド樹脂に2〜
20重量%のポリブタジエンおよび/またはポリビニル
アルコールを相溶させた樹脂で砂を被覆」するようにし
たものが提案されている。In order to solve this problem, Special Publication No. 54-120229
The publication states that ``phenol formaldehyde resin contains 2~
It has been proposed that the sand be coated with a resin in which 20% by weight of polybutadiene and/or polyvinyl alcohol are mixed.
しかしながら、かかる樹脂被覆砂では、樹脂被膜中に崩
壊性を改良するポリブタジエンやポリビニルアルコール
が混合した状態で存在することとなるため、崩壊性が向
上する反面、鋳込時に必要な強度、と《に必要な熱間強
度が得られないといった問題が生じ、鋳物砂として必要
十分な特性を有するとは言い難い問題がある。However, in such resin-coated sand, polybutadiene and polyvinyl alcohol, which improve disintegration properties, are present in the resin coating, so while the disintegration properties are improved, the strength required during casting is There is a problem that the necessary hot strength cannot be obtained, and it is difficult to say that it has necessary and sufficient properties as foundry sand.
また、特開昭52−53723号公報には、「耐火物粒
子の表面をまずビニル系樹脂により被覆し、その上に更
に熱硬化性樹脂によって被覆した」被覆砂が開示されて
いるが、かかる構造のものは、フェノール樹脂等の熱硬
化性樹脂でビニル系樹脂層をさらに被覆する際、両者が
相溶もしくは混合されるため、上記と同様、所期の目的
を有効に達成することができない。Furthermore, JP-A-52-53723 discloses coated sand in which "the surface of refractory particles is first coated with a vinyl resin, and then further coated with a thermosetting resin." With the structure, when the vinyl resin layer is further coated with a thermosetting resin such as phenolic resin, the two become compatible or mixed, so the intended purpose cannot be effectively achieved, similar to the above. .
本発明は、かかる問題に鑑みてなされたものであって、
砂を被覆する樹脂被膜を互いに相溶化させることな《相
互の独立性を保持しうるように2層化し、表層によって
粘結性を保証するとともに、内層側を崩壊性を有する層
とすることによって、熱間強度を保証し、さらに、その
内層によって鋳込後の良好な崩壊性を保証することがで
きる鋳型用樹脂被覆砂の製造法を提案するものである。The present invention has been made in view of such problems, and includes:
The resin coatings that cover the sand are not made to be compatible with each other; they are made into two layers so as to maintain their independence from each other, and the surface layer guarantees caking properties, while the inner layer is made to have disintegrability. The present invention proposes a method for producing resin-coated sand for molds, which can guarantee hot strength and also ensure good disintegration properties after casting due to its inner layer.
本発明にかかる鋳型用樹脂被覆砂の製造法においては、
まず、平均重合度400以下のポリビニルアルコール溶
液もし《はポリ酢酸ビニル溶液を用意し、これを珪砂に
対し、固形分で0.1重量%以上珪砂と混練し、珪砂表
面にポリビニルアルコールもし《はポリ酢酸ビニルを被
覆する。In the method for producing resin-coated sand for molds according to the present invention,
First, prepare a polyvinyl acetate solution with an average degree of polymerization of 400 or less, mix it with silica sand at a solid content of 0.1% by weight or more, and apply polyvinyl alcohol to the surface of the silica sand. Coat polyvinyl acetate.
このポリビニルアルコールもしくはポリ酢酸ビニルは、
平均重合度400以下好ましくは300以下の低い重合
度のものを用いる。This polyvinyl alcohol or polyvinyl acetate is
A polymer having a low average polymerization degree of 400 or less, preferably 300 or less is used.
低重合度のものは、熱間強度の低下を防止するうえで有
効である。Those with a low degree of polymerization are effective in preventing a decrease in hot strength.
市販のポリビニルアルコール、ポリ酢酸ビニルは平均重
合度が高く、そのままで使用すると溶液の粘度が高くな
り、珪砂表向を均一に被覆することが困難となって被覆
不良を生じ、その結果、崩壊性が悪化する。Commercially available polyvinyl alcohol and polyvinyl acetate have a high average degree of polymerization, and when used as is, the viscosity of the solution increases, making it difficult to uniformly coat the surface of silica sand, resulting in poor coating, and as a result, disintegration. becomes worse.
したがって、市販のポリビニルアルコール、ポリ酢酸ビ
ニルは、珪砂と混練する以前に解重合し、必要な程度に
まで粘性を低下させる。Therefore, commercially available polyvinyl alcohol and polyvinyl acetate are depolymerized before being kneaded with silica sand to reduce their viscosity to the required level.
良好な被覆性を得るためには、50重量%濃度の溶液で
、粘度が50〜3000cpの範囲となるような重合度
とすることが好ましい。In order to obtain good coverage, the degree of polymerization is preferably such that the viscosity is in the range of 50 to 3000 cp in a 50% by weight solution.
解重合剤としては、酸素、オゾン、過酸化水素、硝酸カ
リウム、硫酸、重クロム酸カリウム、過マンガン酸カリ
ウム、塩素酸カリウム、サラン粉等を用いることができ
るが、取扱い上過酸化水素を用いることが好ましい。As a depolymerization agent, oxygen, ozone, hydrogen peroxide, potassium nitrate, sulfuric acid, potassium dichromate, potassium permanganate, potassium chlorate, saran powder, etc. can be used, but hydrogen peroxide should be used for handling reasons. is preferred.
ホリビニルアルコールおよびポリ酢酸ヒニルは、夫々単
独で用いることもできるが、ポリ酢酸ビニルの部分ケン
化物を用いることもできる。Although polyvinyl alcohol and polyvinyl acetate can be used alone, a partially saponified product of polyvinyl acetate can also be used.
珪砂に混合するポリビニルアルコールまたはポリ酢酸ビ
ニルは、固形分にして、珪砂に対し0.1重量%以上、
好ましくは0.2〜1.0重量%添加する。The polyvinyl alcohol or polyvinyl acetate to be mixed with the silica sand has a solid content of 0.1% by weight or more based on the silica sand,
Preferably it is added in an amount of 0.2 to 1.0% by weight.
上記のように、珪砂をポリビニルアルコールまたはポリ
酢酸ビニルで被覆したのちには、その被膜をほう素化合
物とアルカリ溶液を添加することによりゲル化させる。As described above, after coating silica sand with polyvinyl alcohol or polyvinyl acetate, the coating is gelled by adding a boron compound and an alkaline solution.
このゲル化処理は、この層とこの層の上に被覆するフェ
ノール樹脂層との相溶を防止し、被膜の熱間強度を向上
させるうえで有効である。This gelling treatment is effective in preventing compatibility between this layer and the phenol resin layer coated on this layer and improving the hot strength of the coating.
ゲル化促進剤としては、ほう酸、ほう酸ソーダ、過ほう
酸、ほう酸亜鉛等のほう素化合物を用いることができる
。As the gelling promoter, boron compounds such as boric acid, sodium borate, perboric acid, and zinc borate can be used.
このゲル化処理に際して、アルカリ溶液をほう素化合物
に加えるようにすると、第1表に示す実験データから明
らかなように、ほう素化合物の添加量を少量化すること
ができることが判明した。It has been found that by adding an alkaline solution to the boron compound during this gelation treatment, the amount of boron compound added can be reduced, as is clear from the experimental data shown in Table 1.
被膜をゲル化した珪砂は、通常の方法により、フェノー
ル樹脂で被覆し、最終的に鋳型用樹脂被覆砂を得る。The silica sand with a gelled coating is coated with a phenol resin by a conventional method to finally obtain resin-coated sand for molds.
この場合、内層としての被膜はゲル化してあるので、フ
ェノール樹脂が内層と相溶することはない。In this case, since the coating as the inner layer is gelled, the phenol resin will not be compatible with the inner layer.
本発明方法に係る鋳型用樹脂被覆砂は、したがって、内
層としてゲル化した低重合度のポリビニルアルコールも
し《はポリ酢酸ビニルの被膜を有し、ゲル化した内層に
相溶せず内層とは独立した層として形成した表層として
フェノール樹脂被膜を有し、表層としてのフェノール樹
脂被膜は、必要な粘結性を与えるとともに、内層として
のゲル化層は、必要な熱間強度を保証し、鋳込時、高熱
にさらされると、粘結部が皆無となって、極めて良好な
崩壊性を示す。Therefore, the resin-coated sand for molds according to the method of the present invention has a coating of gelled polyvinyl alcohol with a low degree of polymerization or polyvinyl acetate as an inner layer, and is not compatible with the gelled inner layer and is independent from the inner layer. The surface phenolic resin coating provides the necessary caking properties, and the inner gelled layer guarantees the necessary hot strength and prevents casting. When exposed to high heat, there is no caking and exhibits extremely good disintegration properties.
本発明方法にかかる樹脂被覆砂は、その良好な崩壊性の
ゆえに、形状が複雑で熱影響の比較的小さい中子にも有
利に適用でき、また、比較的鋳込温度の低い軽合金の鋳
型に有利に適用でき、注湯後、何んらの処理を要するこ
とな《、容易に砂落しをすることができる。Because of its good collapsibility, the resin-coated sand according to the method of the present invention can be advantageously applied to cores with complex shapes and relatively small thermal effects, and can also be advantageously applied to molds of light alloys whose casting temperature is relatively low. It can be advantageously applied to molten metal, and sand can be easily removed without requiring any treatment after pouring.
さらに、本発明方法によれば、フェノール樹脂を用いた
表層の被覆に先立って内層をゲル化するので、フェノー
ル樹脂が内層と相溶することかな《、内層および表層の
機能を夫々独立に維持することができる。Furthermore, according to the method of the present invention, the inner layer is gelled before coating the surface layer with the phenolic resin, so the phenolic resin is compatible with the inner layer (the functions of the inner layer and the surface layer are maintained independently). be able to.
また、本発明方法では、ゲル化処理に際してアルカリ溶
液を用いるので、使用するほう素化合物の量を少量とす
ることができる。Furthermore, in the method of the present invention, since an alkaline solution is used during the gelling treatment, the amount of boron compound used can be reduced.
次に、本発明の実施例を説明する。Next, examples of the present invention will be described.
ケン化度88%、平均重合度600のポリ酢酸ビニルの
部分ケン化物1000gに対し、35%の過酸化水素を
500g、水1675gを加え、95℃で6時間、三つ
口ビーカ中で攪拌して解重合させ、20℃の粘度が2
2 0 CPのポリ酢酸ビニルの部分ケン化物を得た。To 1000 g of partially saponified polyvinyl acetate with a degree of saponification of 88% and an average degree of polymerization of 600, 500 g of 35% hydrogen peroxide and 1675 g of water were added, and the mixture was stirred at 95°C for 6 hours in a three-necked beaker. The viscosity at 20°C is 2.
A partially saponified product of 20 CP polyvinyl acetate was obtained.
次に、150℃に加熱した珪砂10kgに対し、上記ポ
リ酢酸ビニルiooyを添加し、混練機で60秒混練し
た後、ほう酸5gと6 N − Na OH 8 ru
lと水150ml!どの混合物を加えてさらに60秒混
練した後、固形物65%の液状シエルモールド用フェノ
ール樹脂3007を添加し、さばけた後に、ステアリン
酸カルシュウム10グを加えて樹脂被覆砂を得た。Next, the polyvinyl acetate iooy was added to 10 kg of silica sand heated to 150°C, and after kneading for 60 seconds with a kneader, 5 g of boric acid and 8 ru of 6N-NaOH were added.
l and 150ml of water! After which mixture was added and kneaded for an additional 60 seconds, liquid phenol resin 3007 for shell molding with a solid content of 65% was added, and after stirring, 10 g of calcium stearate was added to obtain resin-coated sand.
なお、上記シエルモールド用フェノール樹脂は、フェノ
ールioooyにホルマリン776グ、しゆう酸52を
加えて、95℃で、4.5時間反応させたのち、減圧脱
水し、メタノールを適量加えて生成した。The above phenol resin for shell molds was produced by adding 776 grams of formalin and 52 grams of oxalic acid to phenol iooooy, reacting at 95° C. for 4.5 hours, dehydrating under reduced pressure, and adding an appropriate amount of methanol.
上記方法によって得られた樹脂被覆砂の諸性質を従来の
樹脂被覆砂との比較で第2表に示す。Table 2 shows the properties of the resin-coated sand obtained by the above method in comparison with conventional resin-coated sand.
Claims (1)
ルコールもし《はポリ酢酸ビニルの粘度50〜3000
cpの溶液を固形分で0.1重量%以上添加して混練し
、珪砂表面にポリビニルアルコールもし《はポリ酢酸ビ
ニルを被覆し、次いでほう素化合物とアルカリ溶液を加
えて上記被覆物をゲル化し、その後フェノール樹脂を添
加混練して表面にフェノール樹脂を被覆し、珪砂表面に
ポリビニルアルコールもしくはポリ酢酸ビニルおよびフ
ェノール樹脂を被覆した砂粒を製造することを特徴とす
る鋳型用樹脂被覆砂の製造法。 2 ポリビニルアルコールもし《はポリ酢酸ビニル10
0部に対し、過酸化水素20〜60部加えて解重合させ
たことを特徴とする特許請求の範囲第1項記載の鋳型用
樹脂被覆砂の製造法。 3 ポリビニルアルコールあるいはポリ酢酸ビニルが部
分ケン化物からなることを特徴とする特許請求の範囲第
1項記載の鋳型用樹脂被覆砂の製造法。[Claims] 1. Polyvinyl alcohol with an average degree of polymerization of 400 or less for silica sand;
A solution of 0.1% by weight or more of cp in terms of solid content is added and kneaded, the surface of the silica sand is coated with polyvinyl alcohol or polyvinyl acetate, and then a boron compound and an alkaline solution are added to gel the above coating. A method for producing resin-coated sand for molds, which comprises: adding and kneading a phenol resin to coat the surface with the phenol resin, and producing sand grains with the surface of the silica sand coated with polyvinyl alcohol or polyvinyl acetate and the phenol resin. 2 Polyvinyl alcohol Moshi《Polyvinyl acetate 10
2. The method for producing resin-coated sand for molds according to claim 1, wherein 20 to 60 parts of hydrogen peroxide are added to 0 parts to cause depolymerization. 3. The method for producing resin-coated sand for molds according to claim 1, wherein polyvinyl alcohol or polyvinyl acetate is partially saponified.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55002240A JPS588938B2 (en) | 1980-01-12 | 1980-01-12 | Manufacturing method of resin-coated sand for molds |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55002240A JPS588938B2 (en) | 1980-01-12 | 1980-01-12 | Manufacturing method of resin-coated sand for molds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5699045A JPS5699045A (en) | 1981-08-10 |
| JPS588938B2 true JPS588938B2 (en) | 1983-02-18 |
Family
ID=11523829
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP55002240A Expired JPS588938B2 (en) | 1980-01-12 | 1980-01-12 | Manufacturing method of resin-coated sand for molds |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS588938B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101805554B (en) | 2009-02-16 | 2012-05-30 | 中国科学院金属研究所 | A kind of boron phenolic-titanium nano-composite temperature-resistant and pressure-resistant heavy-duty anti-corrosion coating and its preparation method |
| CN108136485A (en) * | 2015-11-18 | 2018-06-08 | 花王株式会社 | Making molds adhesive composition |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5143969B2 (en) * | 1973-08-17 | 1976-11-25 | ||
| JPS5843169B2 (en) * | 1975-10-29 | 1983-09-26 | 日立金属株式会社 | Resin coated sand |
| JPS5842772B2 (en) * | 1978-03-16 | 1983-09-21 | マツダ株式会社 | Mold manufacturing method |
-
1980
- 1980-01-12 JP JP55002240A patent/JPS588938B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5699045A (en) | 1981-08-10 |
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