JPH0233464B2 - IMONOZUNASOSEIBUTSU - Google Patents
IMONOZUNASOSEIBUTSUInfo
- Publication number
- JPH0233464B2 JPH0233464B2 JP3523283A JP3523283A JPH0233464B2 JP H0233464 B2 JPH0233464 B2 JP H0233464B2 JP 3523283 A JP3523283 A JP 3523283A JP 3523283 A JP3523283 A JP 3523283A JP H0233464 B2 JPH0233464 B2 JP H0233464B2
- Authority
- JP
- Japan
- Prior art keywords
- foundry sand
- inorganic
- mold
- free
- 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 - Lifetime
Links
- 239000004576 sand Substances 0.000 claims description 22
- 239000000203 mixture Substances 0.000 claims description 15
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- 230000001066 destructive effect Effects 0.000 claims description 12
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 6
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims description 5
- 235000011941 Tilia x europaea Nutrition 0.000 claims description 5
- 239000004571 lime Substances 0.000 claims description 5
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 4
- 239000011575 calcium Substances 0.000 claims description 4
- 229910052791 calcium Inorganic materials 0.000 claims description 4
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims description 4
- 239000000395 magnesium oxide Substances 0.000 claims description 3
- 239000011505 plaster Substances 0.000 claims 1
- 238000005266 casting Methods 0.000 description 17
- 239000011230 binding agent Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 6
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000005011 phenolic resin Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000002245 particle Substances 0.000 description 4
- 229920001568 phenolic resin Polymers 0.000 description 4
- 239000000126 substance Substances 0.000 description 3
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000004568 cement Substances 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003110 molding sand Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052925 anhydrite Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 239000011396 hydraulic cement Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C1/00—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
- B22C1/02—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by additives for special purposes, e.g. indicators, breakdown additives
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Mold Materials And Core Materials (AREA)
Description
【発明の詳細な説明】
産業上の利用分野
本発明は鋳物鋳造用鋳型の製造に使用する鋳物
砂組成物に関するものであり、特に鋳造後不要に
なつた鋳型の破壊を容易に行うことができる鋳物
砂組成物に関するものである。[Detailed Description of the Invention] Industrial Application Field The present invention relates to a foundry sand composition used for manufacturing foundry casting molds, and in particular can easily destroy molds that are no longer needed after casting. The present invention relates to a foundry sand composition.
従来技術
鋳物鋳造用鋳型を製造する場合には、その材料
である鋳物砂に、熱硬化性樹脂(例えば、フエノ
ール樹脂、尿素樹脂、フラン系結合樹脂等)を主
成分とする粘結剤或はにかわやポリビニルアルコ
ールを主成分とする粘結剤を混合して使用するこ
とが一般的である。これは鋳物砂に成型性を賦与
すると共に鋳造物を型から取り出すため鋳造後鋳
型の破壊を容易にするためである。鋳物砂に上記
した有機系粘結剤を混ぜてつくつた鋳型を、たと
えば鋳鉄鋳物のように鋳造温度の高い鋳物(1300
〜1400℃)の製造に適用すると、有機系粘結剤は
完全に熱分解して鋳型の機械的強度は著るしく低
下する。この結果小さな外力で鋳型を容易に破壊
することができる。しかしながら、アルミニウム
鋳造のように鋳造温度が650〜750℃と比較的低い
温度の鋳物の製造に適用した場合には、鋳型の外
型は振動その他の比較的小さな外力によつて破壊
することができても、中子は容易には破壊するこ
とができない。これは中子が溶湯に包まれるため
酸素が供給されず、有機系粘結剤が十分分解せ
ず、炭化する結果、中子の機械的強度が十分に低
下しないからである。このため通常は400〜500℃
の温度で4〜10時間いわゆる砂焼きを行つて中子
の機械的強度を低下させるという余分な工程が必
要とされていた。Prior Art When manufacturing molds for casting, a binder or binder whose main component is a thermosetting resin (for example, phenol resin, urea resin, furan-based binding resin, etc.) is added to the foundry sand as the material. It is common to use a mixture of glue and a binder whose main component is polyvinyl alcohol. This is to impart moldability to the foundry sand and to facilitate the destruction of the mold after casting in order to take out the cast product from the mold. A mold made by mixing foundry sand with the organic binder described above is used for castings with high casting temperatures, such as cast iron castings (1300
When applied to production at temperatures up to 1400°C), the organic binder is completely thermally decomposed and the mechanical strength of the mold is significantly reduced. As a result, the mold can be easily destroyed with a small external force. However, when applied to the manufacture of castings where the casting temperature is relatively low (650 to 750°C), such as aluminum casting, the outer mold of the mold can be destroyed by vibration or other relatively small external forces. However, the core cannot be easily destroyed. This is because oxygen is not supplied to the core because it is surrounded by molten metal, and the organic binder is not sufficiently decomposed and carbonized, resulting in insufficient reduction in the mechanical strength of the core. For this reason, it is usually 400 to 500℃.
An extra step was required to reduce the mechanical strength of the core by performing so-called sand firing for 4 to 10 hours at a temperature of .
このような理由から、従来より鋳造後破壊性容
易な中子をつくるため種々の試みが行われてい
る。たとえば、フエノール樹脂粘結剤に硝酸カリ
ウムや硝酸ナトリウムを併用し、鋳造時の温度で
これらの物質を熱分解して酸素を発生させ、フエ
ノール樹脂の燃焼を助ける方法、フエノール樹脂
の代りに変性フエノール樹脂を用いる方法、ある
いはイソシアネートを用いるアシユランド法など
がある。しかしながら、これらのいずれの方法も
十分な効果は得られず、未だ実用化されるに至つ
ていない。 For these reasons, various attempts have been made to create cores that are easily broken after casting. For example, a method that uses potassium nitrate or sodium nitrate in combination with a phenolic resin binder and thermally decomposes these substances at the casting temperature to generate oxygen to help the combustion of the phenolic resin, and a method that uses modified phenolic resin instead of phenolic resin. or the Ashyland method using isocyanate. However, none of these methods achieves sufficient effects and has not yet been put into practical use.
さらにまた上記した有機系粘結剤の代りに水ガ
ラスや水硬性セメントのような無機物質を用いる
方法もある。このような無機系粘結剤は鋳造作業
時に悪臭や有毒ガスを発生させないという優れた
特長がある反面、鋳造後の鋳型の破壊性が小さい
という欠点がある。 Furthermore, there is also a method of using an inorganic substance such as water glass or hydraulic cement instead of the above-mentioned organic binder. Such inorganic binders have the advantage of not emitting bad odor or toxic gas during casting operations, but have the disadvantage that they are less likely to destroy the mold after casting.
発明の目的
したがつて、本発明の目的は鋳造後の鋳物鋳造
用鋳型、特に中子の破壊性を高めた鋳物砂を提供
することにある。OBJECT OF THE INVENTION Accordingly, an object of the present invention is to provide a mold for casting a cast product, particularly a foundry sand with improved breakability of the core.
発明の構成
本発明者は、上記の目的に沿つて鋭意研究を重
ねた結果、鋳物砂に対して無機系破壊剤を1.0な
いし、30.0重量パーセント混合してなる組成物
に、従来使用されている各種の粘結剤を使用して
つくつた鋳型は鋳造後水中に浸漬又は水を散布す
ることによつて容易に破壊することができること
を見出し、本発明を完成した。Composition of the Invention As a result of extensive research in line with the above objectives, the present inventor has discovered that the present inventors have developed a composition comprising 1.0 to 30.0 weight percent of an inorganic destructive agent mixed with foundry sand. The present invention was completed based on the discovery that molds made using various binders can be easily destroyed by immersing them in water or spraying them with water after casting.
本発明において無機系破壊剤とは、水和反応に
ともなう水和物結晶の生成と成長によつて岩石、
コンクリート等のぜい性体を破壊に至らしめる程
の十分な膨張圧を引き起す無機化合物を主要化合
物として含有する薬剤を指称し、セメントコンク
リートの分野ではすでにセメント膨張剤として実
用に供されている。本発明の目的のためには、
(i) カルシウムサルホアルミネート(3CaO・
3Al2O3 CaSO4、以下C3A3CaSo4と略称する)
−遊離石灰−遊離無水せつこう系、
(ii) カルシウムアルミノフエライト(4CaO・
Al2O3・Fe2O3・以下C4AFと略称)−遊離石灰
−遊離マグネシア系、
(iii) アリツト(3CaO・SiO2に少量のAl2O3、
Fe2O3・MgO等が固溶したもの)−遊離石灰−
遊離無水せつこう系、の無機系破砕剤が好まし
く使用される。 In the present invention, the inorganic destructive agent refers to the formation and growth of hydrate crystals associated with hydration reactions, resulting in
It refers to a chemical that contains as a main compound an inorganic compound that causes sufficient expansion pressure to cause the destruction of brittle materials such as concrete, and is already in practical use as a cement expansion agent in the field of cement concrete. . For the purposes of the present invention, (i) calcium sulfoaluminate (3CaO.
3Al 2 O 3 CaSO 4 (hereinafter abbreviated as C 3 A 3 CaSo 4 )
−Free lime−Free anhydrous gypsum system, (ii) Calcium aluminoferrite (4CaO・
Al 2 O 3・Fe 2 O 3・hereinafter abbreviated as C 4 AF) - free lime - free magnesia system, (iii) Alizto (3CaO ・SiO 2 with a small amount of Al 2 O 3 ,
Solid solution of Fe 2 O 3 , MgO, etc.) - Free lime -
Inorganic crushing agents of the free anhydrous gypsum type are preferably used.
無機系破壊剤の混合割合が30.0重量パーセント
を越えると、製造される鋳型の抗折力が小さくな
り鋳型の取扱中あるいは鋳造作業中に鋳型が破損
するおそれがある(通常30Kg/cm2の抗折力を必要
とする)。また、それが1.0重量パーセントより少
ないと十分な破壊効果が得られない。 If the mixing ratio of the inorganic destructive agent exceeds 30.0% by weight, the transverse rupture strength of the manufactured mold will decrease and there is a risk that the mold will break during handling or casting operations (normally, the transverse rupture strength of the mold is 30.0 kg/ cm2 ). ). Moreover, if it is less than 1.0 weight percent, a sufficient destructive effect cannot be obtained.
実施例
以下、本発明を実施例に基づいて説明する。鋳
型の中子の製造に使用されている市販の鋳物砂
に、粒度調整(粒度及び粒径分布を鋳物砂のもの
と整合させること)した無機系破壊剤を添加混合
(添加量:1.0、10.0、20.0、30.0%)して種種の
鋳物砂組成物を調製した。これらの組成物100重
量部に対して3重量部の液状フエノール樹脂を80
℃以上の加熱状態で該組成物にコートし、さらに
これを内寸法10×10×60mmの金型に詰め、300℃
の温度に保つた電気炉に3分間保持して硬化させ
た。これと同時に比較のため無機系破壊剤を含ま
ない鋳物砂を同様な方法によつて成形し硬化させ
た。Examples Hereinafter, the present invention will be explained based on examples. Commercially available foundry sand used for manufacturing mold cores is mixed with an inorganic destructive agent whose particle size is adjusted (to match the particle size and particle size distribution with that of the foundry sand) (addition amount: 1.0, 10.0 , 20.0, 30.0%) to prepare various foundry sand compositions. For each 100 parts by weight of these compositions, 3 parts by weight of liquid phenolic resin was added to 80 parts by weight.
The composition was coated while heated to a temperature of 300°C or above, then packed into a mold with internal dimensions of 10 x 10 x 60 mm, and heated at 300°C.
It was kept in an electric furnace kept at a temperature of 3 minutes to harden it. At the same time, for comparison, molding sand containing no inorganic destructive agent was molded and hardened using the same method.
脱型して得られた試験片を水中に所定時間浸漬
した後取り出し、これをJIS−Z−2602で規定す
る粒度試験方法において使用されるロータツプ形
ふるい分け機械の4メツシユふるいに入れ、下に
受皿を配して5分間ふるい分けを行い、このとき
の試験片の崩壊量を測定した。この試験の結果を
第1図A〜C及び第2図A〜Cに示す。これらの
図において、第1図は後述する試料記号X−1の
鋳物砂、第2図は試料記号X−2の鋳物砂のデー
タに関し、さらにA,B及びC図はそれぞれ試験
片の水中浸漬時間2時間、5時間及び21時間のデ
ータを表わす。また、図中の「崩壊量」は、試験
片の重量に対する上記受皿への落下物の割合(重
量パーセント)を以つて表わした。 The test piece obtained by demolding is immersed in water for a predetermined period of time, then taken out, placed in a 4-mesh sieve of a rotorp type sieving machine used in the particle size testing method specified in JIS-Z-2602, and placed in a saucer underneath. The sample was screened for 5 minutes, and the amount of disintegration of the test piece at this time was measured. The results of this test are shown in Figures 1A-C and 2A-C. In these figures, Figure 1 relates to data for foundry sand with sample code X-1, which will be described later, Figure 2 relates to data on molding sand with sample code Data for times 2 hours, 5 hours and 21 hours are presented. Further, the "amount of collapse" in the figure is expressed as the ratio (weight percent) of the fallen objects to the receiving tray with respect to the weight of the test piece.
(イ) 試料記号X−1:日鉄商事(株)J−30コーテイ
ツドサンド
(ロ) 試料記号X−2:(株)トウチユウRP−20N−
コーテイツドサンド
〔無機系破壊剤〕
(イ) 試料記号S−1:C3A3CaSO440%、
CaSO430%、CaO30%、粉末度ブレーン値1050
cm2/g
(ロ) 試料記号S−2:CaO90%、C4AF7%、
MgO1%、C3S2%、粉末度ブレーン値1050cm2/
g
(ハ) 試料記号S−3:CaO90%、C4AF7%、
MgO1%、C3S2%、粉末度ブレーン値1250cm2/
g
(ニ) 試料記号S−4:CaO90%、C4AF7%、
MgO1%、C3S2%、粉末度ブレーン値1550cm2/
g
(ホ) 試料記号S−5:CaO60%、C3S30%、
CaSO410%、粉末度ブレーン値1550cm2/g
発明の効果
第1図及び第2図のグラフから、本発明に係る
鋳物砂組成物からつくつた鋳型は、水中に浸漬す
るだけで、小さな外力で容易に破壊することがで
きることが判る。
(a) Sample code X-1: Nippon Steel Corporation J-30 coated sand (b) Sample code X-2: Tochiyu Co., Ltd. RP-20N-
Coated sand [Inorganic destructive agent] (a) Sample code S-1: C 3 A 3 CaSO 4 40%,
CaSO4 30%, CaO30%, fineness Blaine value 1050
cm 2 /g (b) Sample code S-2: CaO90%, C 4 AF7%,
MgO1%, C3S2 %, fineness Blaine value 1050cm2 /
g (c) Sample code S-3: CaO90%, C 4 AF7%,
MgO1%, C3S2 %, fineness Blaine value 1250cm2 /
g (d) Sample code S-4: CaO90%, C 4 AF7%,
MgO1%, C3S2 %, fineness Blaine value 1550cm2 /
g (E) Sample code S-5: CaO60%, C3S30 %,
CaSO 4 10%, Blaine fineness value 1550 cm 2 /g Effects of the Invention From the graphs in Figures 1 and 2, it can be seen that the mold made from the foundry sand composition according to the present invention can resist a small external force by simply immersing it in water. It turns out that it can be easily destroyed.
第1図及び第2図は鋳物砂組成物中の無機系破
壊剤の含有量と、この組成物からつくつた成形体
を水中処理したときの崩壊量の関係を示すグラフ
である。
FIGS. 1 and 2 are graphs showing the relationship between the content of an inorganic destructive agent in a foundry sand composition and the amount of disintegration when a molded article made from this composition is treated in water.
Claims (1)
機系破壊剤を混合してなる鋳物砂組成物。 2 無機系破壊剤がカルシウムサルホアルミネー
ト、遊離石灰、遊離無水せつこうからなる特許請
求の範囲第1項記載の鋳物砂組成物。 3 無機系破壊剤がカルシウムアルミノフエライ
ト、遊離石灰及び遊離マグネシアからなる特許請
求の範囲第1項記載の鋳物砂組成物。 4 無機系破壊剤がアリツト、遊離石灰、遊離無
水せつこうからなる特許請求の範囲第1項記載の
鋳物砂組成物。[Claims] 1. A foundry sand composition comprising foundry sand mixed with 1.0 to 30.0% by weight of an inorganic destructive agent. 2. The foundry sand composition according to claim 1, wherein the inorganic destructive agent comprises calcium sulfoaluminate, free lime, and free anhydrous plaster. 3. The foundry sand composition according to claim 1, wherein the inorganic destructive agent comprises calcium aluminoferrite, free lime, and free magnesia. 4. The foundry sand composition according to claim 1, wherein the inorganic destructive agent comprises Aritz, free lime, and free anhydrous gypsum.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3523283A JPH0233464B2 (en) | 1983-03-05 | 1983-03-05 | IMONOZUNASOSEIBUTSU |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3523283A JPH0233464B2 (en) | 1983-03-05 | 1983-03-05 | IMONOZUNASOSEIBUTSU |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59163046A JPS59163046A (en) | 1984-09-14 |
| JPH0233464B2 true JPH0233464B2 (en) | 1990-07-27 |
Family
ID=12436090
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3523283A Expired - Lifetime JPH0233464B2 (en) | 1983-03-05 | 1983-03-05 | IMONOZUNASOSEIBUTSU |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0233464B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4633604B2 (en) * | 2005-08-31 | 2011-02-16 | 有限会社Acreco | Adsorbent production method, adsorbent, adsorbent granule, and adsorbent granule production method |
-
1983
- 1983-03-05 JP JP3523283A patent/JPH0233464B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59163046A (en) | 1984-09-14 |
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