JPH0347647A - Continuous production of sand mold for casting - Google Patents
Continuous production of sand mold for castingInfo
- Publication number
- JPH0347647A JPH0347647A JP17724989A JP17724989A JPH0347647A JP H0347647 A JPH0347647 A JP H0347647A JP 17724989 A JP17724989 A JP 17724989A JP 17724989 A JP17724989 A JP 17724989A JP H0347647 A JPH0347647 A JP H0347647A
- Authority
- JP
- Japan
- Prior art keywords
- sand
- resin
- mold
- solvent
- 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.)
- Pending
Links
- 239000004576 sand Substances 0.000 title claims abstract description 153
- 238000005266 casting Methods 0.000 title abstract 5
- 238000010924 continuous production Methods 0.000 title description 4
- 239000011347 resin Substances 0.000 claims abstract description 65
- 229920005989 resin Polymers 0.000 claims abstract description 65
- 239000002904 solvent Substances 0.000 claims abstract description 52
- 239000011230 binding agent Substances 0.000 claims abstract description 14
- 239000005011 phenolic resin Substances 0.000 claims abstract description 11
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 8
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 8
- 238000004519 manufacturing process Methods 0.000 claims description 30
- 150000001875 compounds Chemical class 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 238000011437 continuous method Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 24
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 abstract description 5
- -1 etc. Substances 0.000 abstract description 5
- 229920001568 phenolic resin Polymers 0.000 abstract description 5
- 238000012856 packing Methods 0.000 abstract description 4
- 239000004848 polyfunctional curative Substances 0.000 abstract 2
- 238000007664 blowing Methods 0.000 description 10
- 239000003208 petroleum Substances 0.000 description 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 150000002576 ketones Chemical class 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- MUXOBHXGJLMRAB-UHFFFAOYSA-N Dimethyl succinate Chemical compound COC(=O)CCC(=O)OC MUXOBHXGJLMRAB-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical group C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethylcyclohexane Chemical compound CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 description 2
- 150000008282 halocarbons Chemical class 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- YUXIBTJKHLUKBD-UHFFFAOYSA-N Dibutyl succinate Chemical compound CCCCOC(=O)CCC(=O)OCCCC YUXIBTJKHLUKBD-UHFFFAOYSA-N 0.000 description 1
- VIZORQUEIQEFRT-UHFFFAOYSA-N Diethyl adipate Chemical compound CCOC(=O)CCCCC(=O)OCC VIZORQUEIQEFRT-UHFFFAOYSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- UDSFAEKRVUSQDD-UHFFFAOYSA-N Dimethyl adipate Chemical compound COC(=O)CCCCC(=O)OC UDSFAEKRVUSQDD-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 235000014676 Phragmites communis Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 229960002097 dibutylsuccinate Drugs 0.000 description 1
- WYACBZDAHNBPPB-UHFFFAOYSA-N diethyl oxalate Chemical compound CCOC(=O)C(=O)OCC WYACBZDAHNBPPB-UHFFFAOYSA-N 0.000 description 1
- XTDYIOOONNVFMA-UHFFFAOYSA-N dimethyl pentanedioate Chemical compound COC(=O)CCCC(=O)OC XTDYIOOONNVFMA-UHFFFAOYSA-N 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003759 ester based solvent Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 238000007528 sand casting Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Mold Materials And Core Materials (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野]
本発明は、樹脂被覆砂の可使時間を伸ばすことにより、
高強度の鋳物用砂型を連続的かつ大量に製造する方法に
関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention provides a method for increasing the pot life of resin-coated sand.
This invention relates to a method for continuously manufacturing high-strength foundry sand molds in large quantities.
〔従来の技術J
従来、高強度の鋳物用砂型の工業的製造方法としては、
その製造に際し樹脂被覆砂の加熱を必要としないためエ
ネルギー消費の点で有利なアシュランド法(例えば、コ
ールドボックス法、ノーベーク法)が知られていた。[Conventional Technology J Conventionally, as an industrial manufacturing method for high-strength foundry sand molds,
The Ashland method (for example, cold box method, no-bake method) is known, which is advantageous in terms of energy consumption because it does not require heating of the resin-coated sand during its production.
例として、アシ1ランドコールドボツクス法による鋳物
用砂型の製造方法について具体的に説明すると次の通り
である。As an example, a method for manufacturing a foundry sand mold by the reed 1 land cold box method will be specifically explained as follows.
フェノール樹脂と溶剤からなる第1成分溶液。A first component solution consisting of a phenolic resin and a solvent.
ポリイソシアネート化合物と溶剤からなる第1!成分溶
液及び鋳物川砂をミキサーで混合することによって樹脂
被覆砂を調製し、これをサンドマガジン(砂貯留槽)に
貯留する。サンドマガジンは、砂型造型時に造型用金型
の上方に配置され、その上部からエアーをブローするこ
とによって、P!4脂被覆被覆砂型内に吹き込まれる。The first one consists of a polyisocyanate compound and a solvent! Resin-coated sand is prepared by mixing the component solution and foundry river sand in a mixer, and is stored in a sand magazine (sand storage tank). The sand magazine is placed above the mold during sand mold making, and by blowing air from the top of the sand magazine, P! 4. Blow into the coated sand mold.
吹き込まれた樹脂被覆砂は、その後アミン等の硬化剤を
透過させることにより常温で硬化し鋳物用砂型が形成さ
れる。The blown resin-coated sand is then hardened at room temperature by passing through a hardening agent such as amine to form a foundry sand mold.
サンドマガジン内に貯留される樹脂被覆砂の量は、従来
の方法によれば金型容量の数十倍から数百倍の範囲内で
あったが、砂型生産効率の観点がらはこの倍率は多けれ
ば多いほど好ましい、しかし、貯留される樹脂被覆砂の
量が増すと、砂型造型時に樹脂被覆砂中にエアーを吹き
込む回数が増えまた樹脂被覆砂の待機時間も長くなるこ
とによって、溶剤が失なわれて、I#l脂被覆被覆砂動
性が低下する。その結果、樹脂被覆砂の金型への充填密
度が下がり、製造した砂型の強度も低下する。According to conventional methods, the amount of resin-coated sand stored in the sand magazine was in the range of several tens to hundreds of times the mold capacity, but from the viewpoint of sand mold production efficiency, this multiplier is not large enough. However, as the amount of resin-coated sand to be stored increases, the number of times air is blown into the resin-coated sand during sand mold making increases, and the waiting time for the resin-coated sand also increases, making it difficult to lose the solvent. As a result, the sand movement of the I#l oil coating is reduced. As a result, the packing density of the resin-coated sand into the mold decreases, and the strength of the manufactured sand mold also decreases.
そこで高強度の鋳物用砂型を効率よく製造するための可
使時間の長い鋳造用樹脂被覆砂の製造方法として、フェ
ノール樹脂とポリイソシアネート化合物とからなる粘結
剤を砂に被覆する前に予め有機溶剤で砂を被覆する方法
が知られていた(特公昭5B−46376号公報参照)
。Therefore, in order to efficiently produce high-strength foundry sand molds, we have developed a method for manufacturing resin-coated sand with a long pot life. A method of coating sand with a solvent was known (see Japanese Patent Publication No. 5B-46376).
.
しかしながら、特に、■サンドマガジン内の貯留量に対
して時間あたりの砂使用量が少ない場合■吹き込み回数
に対して砂の使用量が少ない場合■砂FM右よび湿度の
高い環境などでは、前記従来の鋳造用樹脂被覆砂を使用
する鋳物用砂型の製造方法によっても、サンドマガジン
内に貯留される樹脂被覆砂の量を増やすと依然として樹
脂被覆砂の充填密度が下がり砂型の強度が低下し、実用
的な鋳物用砂型を大量に連続製造することができないと
いう問題があった。However, in particular, ■ When the amount of sand used per hour is small compared to the amount stored in the sand magazine ■ When the amount of sand used per hour is small compared to the number of times of blowing ■ When the sand FM right or in a high humidity environment Even with the manufacturing method of foundry sand molds using resin-coated foundry sand, increasing the amount of resin-coated sand stored in the sand magazine still lowers the packing density of the resin-coated sand and reduces the strength of the sand mold, making it impractical for practical use. There was a problem in that it was not possible to continuously manufacture large quantities of foundry sand molds.
本発明は、前記従来の鋳物用砂型の連続的製造方法の問
題点を解決したもので、高強度の鋳物用砂型を連続的か
つ大量に製造する方法を提供することを目的とする。The present invention solves the problems of the conventional continuous manufacturing method of foundry sand molds, and aims to provide a method for continuously manufacturing high-strength foundry sand molds in large quantities.
〔課題を解決するための手段1
本発明によれば、フェノール樹脂、ポリイソシアネート
化合物、及び溶剤を含む粘結剤溶液と砂とからなる樹脂
被覆砂の一部を砂型製造用金型に導入し、次に硬化剤を
前記金型内に導入する諸工程を繰り返し行なっT成る鋳
物用砂型の連続的製造方法において、前記樹脂被覆砂の
残部に粘結剤用溶剤を適宜追加すること、を特徴とする
flii記方法が提供される。[Means for Solving the Problems 1] According to the present invention, a part of resin-coated sand made of sand and a binder solution containing a phenol resin, a polyisocyanate compound, and a solvent is introduced into a mold for sand mold production. , a continuous method for manufacturing a foundry sand mold comprising repeating various steps of introducing a curing agent into the mold, characterized in that a binder solvent is appropriately added to the remainder of the resin-coated sand. A flii notation method is provided.
本発明において使用される粘結剤溶液は、フェノール樹
脂、ポリイソシアネート化合物及び溶剤を含んで成るも
のである。The binder solution used in the present invention comprises a phenolic resin, a polyisocyanate compound and a solvent.
ここで、フェノール樹脂は、ベンジルエーテル基をその
分子内に有するフェノール、ノボラックあるいはこれら
から誘導される樹脂である。Here, the phenol resin is a phenol having a benzyl ether group in its molecule, a novolak, or a resin derived from these.
ポリイソシアネート化合物としては、例えば、ジフェニ
ルメタンジイソシアネート、ヘキサメチレンジイソシア
ネート、4.4′−ジシクロヘキシルメタンジイソシア
ネートを挙げることができる。Examples of the polyisocyanate compound include diphenylmethane diisocyanate, hexamethylene diisocyanate, and 4,4'-dicyclohexylmethane diisocyanate.
粘結剤用の溶剤としては、アシュランド法における樹脂
被覆砂の調製において使用される溶剤はいずれも本発明
において使用することができる。As the solvent for the binder, any solvent used in the preparation of resin-coated sand in the Ashland process can be used in the present invention.
具体的には、脂肪族炭化水素系、脂環式炭化水素系、芳
香族炭化水素系、ハロゲン化炭化水素系。Specifically, aliphatic hydrocarbons, alicyclic hydrocarbons, aromatic hydrocarbons, and halogenated hydrocarbons.
ケトン系、エステル系、エーテル系、アルコール系等の
有機溶剤を単独でまたは混合して使用することができる
。hA脂脂層覆砂び砂型の製造工程中の温度あるいは溶
剤の毒性、臭気、経済性等の点からは、比較的高沸点(
例λば、180’C以上)の、脂肪族炭化水素系、脂環
式炭化水素系、芳香族炭化水素系、エステル系、ケトン
系の有機溶剤を単独であるいはこれらを混合して使用す
るのが好ましい。Organic solvents such as ketones, esters, ethers, and alcohols can be used alone or in combination. From the viewpoint of the temperature during the manufacturing process of the hA fat-covered sand mold, the toxicity of the solvent, odor, economic efficiency, etc., a relatively high boiling point (
For example, using an aliphatic hydrocarbon-based, alicyclic hydrocarbon-based, aromatic hydrocarbon-based, ester-based, or ketone-based organic solvent with a temperature of 180'C or higher) alone or in combination. is preferred.
具体的には脂肪族炭化水素系溶剤としては。Specifically, as an aliphatic hydrocarbon solvent.
n−ヘキサン、n−へブタン、イソオクタン等の伯に、
灯油、軽油、重油、石油スピリット、石油エーテル、石
油ベンジン等を挙げることができる。脂環式炭化水素系
溶剤としては、シクロヘキサン、エチルシクロヘキサン
等を挙げることができる。芳香族炭化水素系溶剤として
は、ベンゼン、トルエン、キシレン、エチルベンゼン等
を挙げることができる。ハロゲン化炭化水素系溶剤とし
ては、トリクレン、クロルベンゼン等を挙げることがで
きる。ケトン系溶剤としては、メチルエヂルケトン、メ
チルイソブチルケトン、イソホロン、シクロヘキサノン
等を挙げることができる。For example, n-hexane, n-hebutane, isooctane, etc.
Examples include kerosene, light oil, heavy oil, petroleum spirit, petroleum ether, petroleum benzene, and the like. Examples of the alicyclic hydrocarbon solvent include cyclohexane and ethylcyclohexane. Examples of the aromatic hydrocarbon solvent include benzene, toluene, xylene, and ethylbenzene. Examples of the halogenated hydrocarbon solvent include trichlene and chlorobenzene. Examples of the ketone solvent include methyl edyl ketone, methyl isobutyl ketone, isophorone, and cyclohexanone.
エステル系溶剤としては、酢酸エチル、アジピン酸ジメ
チル、アジピン酸ジエチル、グルタル酸ジメチル、コハ
ク酸ジメチル、コハク酸ジブチル、シュウ酸ジエチル、
フタル酸ジエチル等を挙げることができる。エーテル系
溶剤としては、イソプロピルエーテル、1.4−ジオキ
サン等を挙げることができる、アルコール系溶剤として
は、エタノール、エチレングリコール、イソプロパツー
ル、フルフリルアルコール等を挙げることができる。Ester solvents include ethyl acetate, dimethyl adipate, diethyl adipate, dimethyl glutarate, dimethyl succinate, dibutyl succinate, diethyl oxalate,
Examples include diethyl phthalate. Examples of the ether solvent include isopropyl ether and 1,4-dioxane, and examples of the alcohol solvent include ethanol, ethylene glycol, isopropanol, and furfuryl alcohol.
粘結剤溶液は、所望により劣化防止剤、乾燥防止剤等の
他の成分を含むことができる。The binder solution may contain other components such as anti-deterioration agents and anti-drying agents, if desired.
本発明において使用される砂は、微粉状の砂。The sand used in the present invention is finely powdered sand.
粘度質の砂、再生砂等を含むあらゆる種類の砂であるが
、通常の鋳物砂が好ましく、50〜600μ程度の砂が
特に好ましい。Although all kinds of sand including viscous sand, recycled sand, etc. are used, ordinary foundry sand is preferable, and sand of about 50 to 600 μm is particularly preferable.
フェノール樹脂、ポリイソシアネート化合物あるいは溶
剤各々の砂に対する配合割合は、砂型の強度の点から、
それぞれ砂に対し全て0.01〜10重量%の範囲が好
ましく、特に0.1〜5.0重量%の範囲が好ましい。The proportion of phenol resin, polyisocyanate compound, or solvent to sand is determined based on the strength of the sand mold.
Preferably, each content is in the range of 0.01 to 10% by weight, particularly preferably 0.1 to 5.0% by weight, based on the sand.
樹脂被覆砂の調製は、例えばフェノール樹脂、ポリイソ
シアネート化合物及び溶剤から成る粘結剤溶液と砂とを
、好ましくは一10〜50℃の範囲の温度で、ミキサー
により四成分が均一に混合するように十分に混練するこ
とによって行なうことができる。Preparation of resin-coated sand involves, for example, mixing sand and a binder solution consisting of a phenolic resin, a polyisocyanate compound, and a solvent, preferably at a temperature in the range of -10 to 50°C, using a mixer so that the four components are uniformly mixed. This can be done by thoroughly kneading the mixture.
粘結剤γ8液は、あらかじめフェノール樹脂溶液とイン
シアネート化合物溶液とを調製しておき、砂と混線時に
両者を砂に添加することが特に好ましい。It is particularly preferable that the binder γ8 liquid is prepared in advance as a phenol resin solution and an incyanate compound solution, and that both are added to the sand at the time of crosstalk with the sand.
調製した樹脂被覆砂をサンドマガジン内に貯留し、例え
ば、エアーによる吹き込みによって所望量の樹脂波I砂
を砂型製造用金型内に導入し1次に、塩基、アミン、金
属イオン等のアシ五ランド法において通常使用される硬
化剤を砂型が硬化するに十分な量だけ、前記金型内に導
入することによって鋳物用砂型を製造する。The prepared resin-coated sand is stored in a sand magazine, and a desired amount of resin-coated sand is introduced into a sand mold manufacturing mold by, for example, blowing with air. A foundry sand mold is manufactured by introducing into the mold a curing agent commonly used in the land method in an amount sufficient to harden the sand mold.
次いで、サンドマガジン内に残留している未使用の樹脂
被覆砂にオイラーなどにより連続的に溶剤蒸気を追加さ
れ均一全体に浸透された所望量の樹脂被覆砂を砂型製造
用金型内に導入し次に硬化剤を導入する諸工程をくり返
すことによって、連続的に鋳物用砂型を製造することが
できる。Next, solvent vapor is continuously added to the unused resin-coated sand remaining in the sand magazine using an oiler, etc., and the desired amount of resin-coated sand is introduced into the sand mold manufacturing mold. Next, by repeating the steps of introducing a hardening agent, foundry sand molds can be manufactured continuously.
ここで使用する溶剤は、前記の粘結剤用の溶剤ど同じ種
類のものであるが、樹脂被覆砂の調製の際に使用した溶
剤と同じものであっても異なるものであっても良い。The solvent used here is of the same type as the binder solvent described above, but it may be the same or different from the solvent used in preparing the resin-coated sand.
鋳物用砂型の連続的製造の随意の時点において残留して
いる樹脂mru砂中における溶剤の量は。The amount of solvent in the resin MRU sand remaining at any point in the continuous production of foundry sand molds is:
使用される溶剤の種類、砂型製造工程中の温度、操作方
法、製造される砂型の重量等の諸条件により種々異なる
ため、それに合わせて添加する溶剤の量を調節する必要
がある。樹脂被覆砂の可使時間の延長及び砂をの強度の
確保の点からは1例えば、250gの砂型300個製造
あたり、樹脂被覆砂の調製直後における溶剤含有量(す
なわち樹脂被覆砂中における瀉剤の初期含有ff1)の
10〜80%の潰の溶剤を、連続的砂型製造工程におい
て樹脂被覆砂に均等に追加するのが好ましく。Since it varies depending on various conditions such as the type of solvent used, the temperature during the sand mold manufacturing process, the operating method, and the weight of the sand mold to be manufactured, it is necessary to adjust the amount of solvent added accordingly. From the point of view of extending the pot life of resin-coated sand and ensuring the strength of the sand, for example, the solvent content immediately after preparation of resin-coated sand (i.e., the amount of diaphragm in resin-coated sand is Preferably, 10 to 80% of the initial content ff1) of solvent is added evenly to the resin-coated sand in a continuous sand casting process.
15〜50%の量の溶剤を追加するのが特に好ましい。Particular preference is given to adding solvent in an amount of 15 to 50%.
残留している樹脂被覆砂に溶剤を添加する方法としては
、サンドマガジンの上部の口から樹脂1t1)′I!砂
にスプレーにより直接溶剤を吹き付ける方法、樹脂被覆
砂を金型に導入する際に溶剤蒸気又は霧化溶剤を含有さ
せたエアーを使用する方法等がある。A method of adding a solvent to the remaining resin-coated sand is to add resin 1t1)'I! from the opening at the top of the sand magazine. There are methods such as spraying the solvent directly onto the sand, and using air containing solvent vapor or atomized solvent when introducing the resin-coated sand into the mold.
鋳物用砂型の製造工程中で、樹脂被覆砂中の溶剤が失な
われると、その流動性が損なわれる。During the manufacturing process of foundry sand molds, when the solvent in the resin-coated sand is lost, its fluidity is impaired.
そこで、砂型の連続的製造における2個目以降の鋳物用
砂型の製造において樹脂被覆砂に溶剤を適宜追加すると
、樹脂′IIrH砂の調製直後におけるその流動性がほ
ぼ確保される。そのため、金型内に十分な充填密度で樹
脂被覆砂が導入され、キユアリングにより高強度の鋳物
用砂型が製造されることになる。Therefore, if a solvent is appropriately added to the resin-coated sand in the production of the second and subsequent foundry sand molds in the continuous production of sand molds, the fluidity of the resin 'IIrH sand immediately after its preparation is almost ensured. Therefore, the resin-coated sand is introduced into the mold at a sufficient packing density, and a high-strength foundry sand mold is manufactured by curing.
すなわち、鋳物用砂型の連続的製造において樹脂被覆砂
に溶剤を追加することにより、−度に多量に調製した樹
脂被覆砂を砂型の連続大量製造に使用することのできる
時間を、著るしく延長することが可能となった。That is, by adding a solvent to the resin-coated sand in the continuous production of foundry sand molds, the time during which the resin-coated sand prepared in large quantities at one time can be used for the continuous mass production of sand molds is significantly extended. It became possible to do so.
〔実施例]
以下、実施例及び比較例により本発明をさらに詳細に説
明する。以下、「部」は全て「重量部」を「%」は全て
「重量%」を意味する。[Example] Hereinafter, the present invention will be explained in more detail with reference to Examples and Comparative Examples. Hereinafter, all "parts" mean "parts by weight" and all "%" mean "% by weight".
X血廻ユ
保土谷化学工業(掬製ベンジルエーテル基含有フェノー
ル樹脂52.0%、コハク酸ジメチルエステル17.5
%、石油系溶剤(丸首石油■製5W−1800)30.
5%から成る溶液を調製して第!成分溶液とした。X Kekaiyu Hodogaya Chemical Industry (Kiku made benzyl ether group-containing phenol resin 52.0%, succinic acid dimethyl ester 17.5%
%, petroleum solvent (5W-1800 manufactured by Marukubi Sekiyu ■) 30.
Prepare a solution consisting of 5% and proceed! A component solution was prepared.
Bll Lこ、ジフェニルメタンジイソシアネート(日
本ポリウレタン工業■製MR−200)75.0%1石
油系溶剤(出光興産■製IP−150)25.0%から
成る溶液を調製して第1)成分溶液とした。Prepare a solution consisting of 75.0% diphenylmethane diisocyanate (MR-200, manufactured by Nippon Polyurethane Industries) and 25.0% petroleum solvent (IP-150, manufactured by Idemitsu Kosan), and add the first) component solution. did.
鋳物用の水洗した遠州砂280000部に前記第■成分
溶液3080部及び前記第1I成分溶液3080部を添
加しながら、品用式ミキサーで14 Or、p、mにて
60秒間混練りして樹脂被覆砂286160部を調製し
た。調製した樹脂被覆砂をサンドマガジン内に移した。Adding 3080 parts of the above No. 1 component solution and 3080 parts of the above 1I component solution to 280000 parts of water-washed Enshu sand for foundry, the mixture was kneaded for 60 seconds at 14 Or, p, m using a grade mixer to obtain a resin. 286,160 parts of coated sand were prepared. The prepared resin-coated sand was transferred into a sand magazine.
サンドマガジン内に3.0kg/crn”のゲージ圧で
エアーを2秒間ずつ2回ブローして、樹脂被覆砂をカム
シャフト中子製造用金型内に吹き込んだ、この工程を計
4分間実施して、樹脂被覆砂を60個のカムシャフト中
子製造用金型内に吹き込んだ0次に、2.5k g /
c rn’のゲージ圧で1秒間トリエチルアミンをジ
ェネレーターによりガツシングし前記金型内に透過させ
てキユアリングした後、3.0kg/crrl”のゲー
ジ圧でエアーパージして、250gの川Mのカムシャフ
ト中子砂型を計60個製造した。なお作業温度、砂の温
度は共に約20℃、相対湿度は56%であり、使用機械
は新東工業■製コールドボックスマシンである。Air was blown into the sand magazine at a gauge pressure of 3.0 kg/crn twice for 2 seconds each, and the resin-coated sand was blown into the mold for manufacturing the camshaft core. This process was carried out for a total of 4 minutes. Then, resin-coated sand was blown into 60 molds for manufacturing camshaft cores at a rate of 2.5 kg/
After gassing triethylamine with a generator for 1 second at a gauge pressure of crn' and permeating it into the mold for curing, air purging was performed at a gauge pressure of 3.0 kg/crrl, and a camshaft of 250 g was poured into the camshaft. A total of 60 child sand molds were manufactured.The working temperature and the sand temperature were both approximately 20°C, the relative humidity was 56%, and the machine used was a cold box machine manufactured by Shinto Kogyo ■.
金を内への樹脂被覆砂の吹き込み、キユアリング等の一
連の前記工程を、順次、樹脂被覆砂調製の30分後、6
0分後、80分擾、100分後、120分後、140分
後に各60回、計420回連続的に繰り返して、最初の
砂型の製造から140分間で、250gのff1flの
カムシャフト中子砂をを総計420個製造した。なお、
ここで樹脂>1)1)砂の金型内への吹き込み工程(前
記140分間)において、エアーは石油系溶剤(丸首石
油■製5W−1800及び出光興産■製IP−150)
の入ったオイラーを通過させて本溶剤を霧状にして含有
させたエアーを使用し、樹脂被覆砂調製後、その30分
後、60分後、80分後、100分後、120分後に各
90部、合計で540部の前記溶剤が樹脂被覆砂に均等
に添加されるようにして一連の前記連続工程を実施した
。A series of the above steps such as blowing the resin-coated sand into the gold and curing were carried out 30 minutes after the preparation of the resin-coated sand.
After 0 minutes, 80 minutes, 100 minutes, 120 minutes, and 140 minutes, the process was repeated 60 times each, for a total of 420 times.A 250g ff1fl camshaft core was produced in 140 minutes from the initial sand mold production. A total of 420 pieces of sand were manufactured. In addition,
Here, resin>1) 1) In the step of blowing sand into the mold (140 minutes), the air is petroleum-based solvent (5W-1800 manufactured by Marukubi Sekiyu and IP-150 manufactured by Idemitsu Kosan).
After preparing the resin-coated sand, 30 minutes, 60 minutes, 80 minutes, 100 minutes, and 120 minutes have passed through an oiler containing this solvent. The series of successive steps was carried out such that 90 parts of the solvent, 540 parts in total, were added evenly to the resin-coated sand.
製造してlO゛分後における砂型の引張り強度は、42
0個全個全ついて6.6〜17.2kgf/ c rr
i″の範囲内であり、いずれも実用上の基準6.0kg
r/cm’をこえており充分実用的であった。The tensile strength of the sand mold after 10 minutes of manufacture is 42
6.6 to 17.2 kgf/c rr with all 0 pieces
i'', both of which are within the practical standard of 6.0 kg.
r/cm' and was sufficiently practical.
実Uヱ
樹脂被覆砂の金型内への吹き込み工程において1石油系
溶剤を霧状にして含有させたエアーを、樹脂被覆砂調製
の30分後、60分後、80分後、100分後、120
分後、140分後。In the process of blowing resin-coated sand into the mold, air containing atomized petroleum solvent was applied 30 minutes, 60 minutes, 80 minutes, and 100 minutes after preparing the resin-coated sand. , 120
Minutes later, 140 minutes later.
160分後、180分後、200分後、220分後、2
40分後に各125部1合計で1375部の前記溶剤が
樹脂被覆砂に均等に添加されるようにした以外は実施例
1と同様にして、樹脂被覆砂の吹き込み、キユアリング
等の一連の前記連続工程を実施して、250gの重量の
カムシャフト中子砂型を総計720個製造した。製造し
て10分後における砂型の引っ張り強度は、720個全
Irついて1O32〜16.5kgf/cばの範囲内で
あり、いずれも実用上の基準6.0kgf’/crn’
をはるかに越λており十分実用的であった。After 160 minutes, after 180 minutes, after 200 minutes, after 220 minutes, 2
A series of the above-mentioned continuous steps such as blowing and curing of the resin-coated sand were carried out in the same manner as in Example 1, except that 125 parts each (1375 parts in total) of the solvent was added evenly to the resin-coated sand after 40 minutes. The process was carried out to produce a total of 720 camshaft core sand molds weighing 250 g. The tensile strength of the sand mold 10 minutes after manufacturing was within the range of 1O32 to 16.5 kgf/c for all 720 Ir pieces, both of which met the practical standard of 6.0 kgf'/crn'.
It was far beyond λ and was sufficiently practical.
X胤拠旦
樹脂FtLm砂の金型内への吹き込み工程において、石
油系溶剤を霧状にして含有させたエアーを、樹脂mm砂
調製の30分後、60分後、80分後、100分後、1
20分後、140分後、160分後、180分後に各2
25部1合計で1800部の前記溶剤が樹脂被覆砂に均
等に添加されるようにした以外は実施例1と同様にして
、樹脂被覆砂の吹き込み、キユアリング等の一連の前記
連続工程を実施して、250gのlTlff1のカムシ
ャフト中子砂をを総計540個製造した。製造して10
分後における砂型の引っ張り強度は、540個全Irつ
いて8.5〜18.6kgf/Cゴの範囲内であり、い
ずれも実用上の基準6.0kgf/crr/をはるかに
越えており十分実用的であった。In the process of blowing the resin FtLm sand into the mold, air containing atomized petroleum solvent was applied for 30 minutes, 60 minutes, 80 minutes, and 100 minutes after preparing the resin mm sand. After, 1
2 each after 20 minutes, 140 minutes, 160 minutes, and 180 minutes.
A series of continuous steps such as blowing the resin-coated sand and curing were carried out in the same manner as in Example 1, except that a total of 1,800 parts of the solvent was added evenly to the resin-coated sand. A total of 540 camshaft core sands of 250 g of lTlff1 were produced. Manufacture 10
The tensile strength of the sand mold after 10 minutes was within the range of 8.5 to 18.6 kgf/C for all 540 Ir pieces, far exceeding the practical standard of 6.0 kgf/crr/, and sufficient for practical use. It was a target.
比較10゜
樹脂被覆砂の金型内への吹き込み工程に右いて、エアー
中に溶剤を含(1せしめないで、それ以外の点は実施例
1と同様にして、250gのfftffiのカムシャフ
ト中子砂型を連続的に製造した。Comparison 10: During the process of blowing resin-coated sand into the mold, the air was not mixed with a solvent (1), and the other points were the same as in Example 1. Child sand molds were manufactured continuously.
その結果、製造して10分後における砂型の引張強度が
6.0kgf/crn’以上の実用的な砂型を、最初の
砂型の製造から約80分の時点で。As a result, a practical sand mold with a tensile strength of 6.0 kgf/crn' or more after 10 minutes of manufacture was obtained at about 80 minutes from the time of manufacture of the first sand mold.
180個製造することができた。しかし、最初の砂型の
製造から約80分を越えて製造したものは、その引張り
強度が極めて低く、実用には供することができないもの
であった。We were able to manufacture 180 pieces. However, sand molds manufactured more than 80 minutes after the initial sand mold manufacture had extremely low tensile strength and could not be put to practical use.
〔発明の効果1
以上説明した通り1本発明の方法により、樹脂被覆砂の
可使時間を大幅に伸ばすことができたため、高強度の鋳
物用砂型を簡易かつ経済的に連続して大量に製造するこ
とが可能となり、その実用的意義は極めて大きい。[Effects of the invention 1 As explained above, 1 The method of the present invention makes it possible to significantly extend the usable life of resin-coated sand, making it possible to easily and economically continuously produce large quantities of high-strength foundry sand molds. This makes it possible to do this, and its practical significance is extremely large.
Claims (1)
溶剤を含む粘結剤溶液と砂とからなる樹脂被覆砂の一部
を砂型製造用金型に導入し、次に硬化剤を前記金型内に
導入する諸工程を繰り返し行なって成る鋳物用砂型の連
続的製造方法において、前記樹脂被覆砂の残部に粘結剤
用溶剤を適宜追加すること、を特徴とする前記方法。(1) A portion of resin-coated sand consisting of sand and a binder solution containing a phenol resin, a polyisocyanate compound, and a solvent is introduced into a sand mold manufacturing mold, and then a curing agent is introduced into the mold. 1. A continuous method for producing foundry sand molds comprising repeating various steps, characterized in that a binder solvent is appropriately added to the remainder of the resin-coated sand.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17724989A JPH0347647A (en) | 1989-07-11 | 1989-07-11 | Continuous production of sand mold for casting |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17724989A JPH0347647A (en) | 1989-07-11 | 1989-07-11 | Continuous production of sand mold for casting |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0347647A true JPH0347647A (en) | 1991-02-28 |
Family
ID=16027768
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP17724989A Pending JPH0347647A (en) | 1989-07-11 | 1989-07-11 | Continuous production of sand mold for casting |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0347647A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5849246A (en) * | 1994-08-24 | 1998-12-15 | Otsuka Pharmaceutical Factory, Inc. | Apparatus for spray sterilization and method therefor |
JP2019502768A (en) * | 2015-10-30 | 2019-01-31 | アーエスカー ケミカルズ エルエルシー | Polyurethane binder containing alcohol solvent |
-
1989
- 1989-07-11 JP JP17724989A patent/JPH0347647A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5849246A (en) * | 1994-08-24 | 1998-12-15 | Otsuka Pharmaceutical Factory, Inc. | Apparatus for spray sterilization and method therefor |
JP2019502768A (en) * | 2015-10-30 | 2019-01-31 | アーエスカー ケミカルズ エルエルシー | Polyurethane binder containing alcohol solvent |
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