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JPS6230063B2 - - Google Patents
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JPS6230063B2 - - Google Patents

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Publication number
JPS6230063B2
JPS6230063B2 JP54102175A JP10217579A JPS6230063B2 JP S6230063 B2 JPS6230063 B2 JP S6230063B2 JP 54102175 A JP54102175 A JP 54102175A JP 10217579 A JP10217579 A JP 10217579A JP S6230063 B2 JPS6230063 B2 JP S6230063B2
Authority
JP
Japan
Prior art keywords
weight
parts
sand
powder
granular
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
Application number
JP54102175A
Other languages
Japanese (ja)
Other versions
JPS5626654A (en
Inventor
Yutaka Hatano
Shunichi Arikawa
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Artience Co Ltd
Original Assignee
Toyo Ink Mfg Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Toyo Ink Mfg Co Ltd filed Critical Toyo Ink Mfg Co Ltd
Priority to JP10217579A priority Critical patent/JPS5626654A/en
Publication of JPS5626654A publication Critical patent/JPS5626654A/en
Publication of JPS6230063B2 publication Critical patent/JPS6230063B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は鋳型砂崩壊剤改良に関するものであ
る。 水ガラス系鋳型やセメント系鋳型は成型が容易
で材料費も安価であることから鋳物製造における
利用度は極めて高いが、鋳型に注湯(金属の溶解
したものを湯と云い、その湯を鋳型え流し込むこ
と)して凝固させた後、鋳型を破壊して製品を取
り出す時に鋳型砂の崩壊性が悪く、砂落し作業に
手間がかかり、ニユーマチツクハンマーや、大ハ
ンマー等を利用して作業をするため作業者の疲労
も大きく作業に多大の労力を要し、又ハンマーの
衝撃によつて鋳物にひび割れが入り不良品になる
等、そのため時には生産性を阻害する。これは水
ガラス系鋳型やセメント系鋳型の最大の欠点であ
り、この欠点を改良するために糖密、蔗糖、ブド
ウ糖、澱粉等水溶性補助粘結剤や、木粉、ピツチ
コークス粉、石炭粉等を崩壊剤として使用してい
るが崩壊性改良の面で顕著な結果が得られていな
い。これは木粉等粉体の崩壊剤を多用すれば崩壊
性は向上するが粉体の表面積が多くなるため粘結
剤の水ガラスやセメントの結合力が低下し、常温
での鋳型の強度が弱くなり、鋳型の表面安定性も
悪く、取り扱いが困難となる。蔗糖等水溶性補助
粘結剤は水ガラスに含まれている水に溶かされて
砂の粘結力が強くなり、砂の流動性が悪くなつて
成型に手間がかかる。又水ガラスは水溶性補助粘
結剤に水分を取られるため混練砂の乾燥が早くな
り砂の可使用時間が短かく、CO2ガス型砂の場合
混練砂の貯蔵が出来ない。セメント鋳型の場合糖
蜜を使用するが、砂が発熱して木型(鋳型を造る
模型)の損耗が大きく、又不快な臭いを発生す
る。蔗糖、ブドウ糖は液糖になると崩壊剤として
の効果が減退する、鋳型砂の混練中又は混練後に
吸水した崩壊剤等は脱水が困難で、その残留水分
のために鋳型は強度が低下して表面安定性も悪く
なる。そのため蔗糖、ブドウ糖、澱粉等は粉、粒
状の状態で鋳型砂砂粒間に点在させて、注湯の際
高温の湯によつて加熱され燃焼して炭化し、鋳物
が凝固する過程において発生する圧縮力を吸収す
る緩衝効果を発揮するが、水に溶けたものはこの
緩衝効果が低下するため鋳型砂は締つけられて崩
壊性が悪くなる。特に中子(鋳物の内側の鋳型)
はその傾向が大きい。又水溶性補助粘結剤を使用
した鋳型は吸湿性があり、鋳型の乾燥を充分にし
てないと鋳物にガス欠陥が発生する。これまで崩
壊剤を多用すれば崩壊性は向上するが材料費が高
くなり、鋳型強度や表面安定性が劣下し注湯の際
に可燃物の燃焼によるガス発生が多くなり、鋳物
はガス欠陥による不良が多発する。従来水ガラス
系鋳型砂やセメント系鋳型砂は安価のため使い捨
られていたが産業廃棄物処理の規制が厳しくなる
にしたがつて廃棄物処理費用が鋳物製造原価に占
める割合が大きくなり、砂の回収再生利用が急務
となつて再製装置の設置が広く行なわれるように
なつたが、崩壊性の悪い砂は砂粒表面に硬化した
結合剤が多く固着し、砂粒が固く結合して大きな
砂塊となり、これを破砕機にかけて砕き、砂粒表
面に固着した異物は砂粒精磨機にかけて除去する
等多くの手間がかかるわりに砂粒が破砕されて回
収率が悪く、切角再生しても半数の砂は産業廃棄
物として処理されている。粉、粒状の石油系ワツ
クス、粉、粒状の植物系ワツクス、粉、粒状の動
物系ワツクス(以後上記各種ワツクスを総称して
粉、粒状のワツクスと表現する場合がある)、
粉、粒状の低分子量ポリオレフイン樹脂、粉、粒
状のアタクチツクポリプロピレン樹脂、粉、粒状
の化学構造不明の所謂釜残樹脂状物(以後上記各
種樹脂及び樹脂状物を総称して粉、粒状のポリオ
レフイン樹脂等と表現する場合がある)の1種又
は2種以上からなる鋳型砂崩壊剤は顕著な崩壊性
を発揮し、砂の再製副用率も高いが軟質のため混
練中に圧しつぶされて混練機に附着したり、夏期
や作業場の室温の高い所では軟化するため取り扱
いに手間がかかり、又注湯の際燃焼して不快な臭
いを発生するため作業環境を悪くする。 本発明は鋳型砂崩壊剤として顕著な効果のある
粉、粒状の石油系ワツクス、粉、粒状の植物系ワ
ツクス、粉、粒状の動物系ワツクス、粉、粒状の
低分子量ポリオレフイン樹脂、粉、粒状のアタク
チツクポリプロピレン樹脂、粉、粒状の化学構造
不明の所謂釜残樹脂状物の硬度を高め、不快な臭
いの消臭剤として粉、粒状の黒鉛、木粉、籾殻の
粉、粒状の粉砕物、穀類の粉、粒状の粉砕物、
粉、粒状の澱粉(以後上記各種消臭剤を総称して
消臭剤と表現する場合がある)の1種又は2種以
上を添加混合するものである。 本発明の特長とするところは粉、粒状の石油系
ワツクス、粉、粒状の植物系ワツクス、粉、粒状
の動物系ワツクス、粉、粒状の低分子量ポリオレ
フイン樹脂、粉、粒状のアタクチツクポリプロピ
レン樹脂、粉、粒状の化学構造不明の所謂釜残樹
脂状物の1種又は2種以上を粉、粒状の黒鉛、木
粉、籾殻の粉、粒状の粉砕物、穀類の粉、粒状の
粉砕物、粉、粒状の澱粉の1種又は2種以上から
なる消臭剤の表面に塗布して防水被膜を施したも
のを水ガラス系鋳型砂やセメント系鋳型砂に添加
する。その新しく開発された鋳型砂崩壊剤を添加
した鋳型砂は、砂の流動性が良くなり、鋳型砂の
搗き固め作業が軽減されて成型が容易に出来る、
又吸水性の物質は防水加工を施してあるから粘結
剤に必要な水分を吸着しないため混練砂の可使用
時間も長く、常温における鋳型の表面安定性も良
好で、水ガラス系鋳型砂の場合には水ガラスの添
加量を従来の水ガラス系鋳型砂よりも少なくする
ことが出来る。砂粒間に分散して点在する鋳型砂
崩壊剤は注湯の際高温の湯に熱せられて鋳型砂が
膨脹する前に融解溶出し、その流動性は極めて良
く砂粒間の間隙に広く流出分散し、特に水ガラス
系鋳型砂の場合には硬化した水ガラスが高温高圧
下で軟化する前に砂粒や結合剤の表面に炭化膜を
形成して結合剤の粘着を防止する。この鋳型砂崩
壊剤が溶出した跡には小さい空洞が出来て鋳型を
多孔質化し、湯温によつて膨脹する砂や、鋳物が
凝固する過程において発生する圧縮力の緩衝部と
なり、圧縮力を吸収して鋳型の破壊を防止する。
鋳型は鋳込後の残留熱量の大きいほど鋳型砂崩壊
剤の溶出炭化範囲が広くなり、極めて顕著な崩壊
性を示す。消臭剤は砂粒間に分散して点在し、注
湯の際高温の湯で熱せられて黒鉛以外の物質は炭
化する。この炭化物は湯温によつて膨脹する砂
や、鋳物が凝固する過程において発生する圧縮力
を吸収する緩衝材となり崩壊性向上の補助的効果
を発揮するばかりでなく、粉、粒状のワツクスや
粉、粒状の低分子量ポリオレフイン樹脂等が燃焼
する時に発生する不快な臭いは、消臭剤の添加混
合によつて融点が高くなるにしたがつて燃焼温度
も高温側へ移行し、高温燃焼させることによつて
消臭する、この消臭作用は作業環境を良くする重
要な役割りを果す。 本発明を更に詳細に説明するならば、消臭剤と
して添加される粉、粒状の黒鉛、木粉、籾殻の
粉、粒状の粉砕物、穀類の粉、粒状の粉砕物、
粉、粒状の澱粉の1種又は2種以上を粉、粒状の
石油系ワツクス、粉、粒状の植物系ワツクス、
粉、粒状の動物系ワツクス、粉、粒状の低分子量
ポリオレフイン樹脂、粉、粒状のアタクチツクポ
リプロピレン樹脂、粉、粒状の化学構造不明の所
謂釜残樹脂状物の1種又は2種以上に5〜100重
量部の範囲内が望ましい、この消臭剤の防水加工
はヘンシエルミキサーを用いた、ヘンシエルミキ
サーは撹拌部の外壁に冷却水用のジヤケツトを備
え、このミキサーに粉、粒状のワツクス又は粉、
粒状の低分子量ポリオレフイン樹脂等の内の1種
又は2種以上を100重量部と、消臭剤の内の1種
又は2種以上を5〜100重量部の範囲内を同時に
入れて撹拌すると混練中に粉、粒状のワツクスや
粉、粒状の低分子量ポリオレフイン樹脂等と消臭
剤は摩擦によつて50℃前后の熱を持ち、この熱に
よつて粉、粒状のワツクスや粉、粒状の低分子量
ポリオレフイン樹脂等は軟化して消臭剤の表面に
附着して防水被膜を形成する。防水被膜を施した
消臭剤はヘンシエルミキサーの冷却水用ジヤケツ
トに送水して撹拌しながら冷却し、粉、粒状のワ
ツクスや粉、粒状の低分子量ポリオレフイン樹脂
等と消臭剤とが固りになつたり、消臭剤の防水被
膜の剥離を防止し、流動性の良好な鋳型砂崩壊剤
を得ることが出来る。この防水加工を施す撹拌機
は、ヘンシエルミキサーに限らず、撹拌中に粉、
粒状のワツクスや粉、粒状の低分子量ポリオレフ
イン樹脂等及び消臭剤が粉砕されたり、圧しつぶ
されることがなく、摩擦熱によつて粉、粒状のワ
ツクスや粉、粒状の低分子量ポリオレフイン樹脂
等が融解しなければ、どのような型の撹拌機でも
よく、又冷却は冷却水を用いなくてもよい。この
場合には防水加工完了した鋳型砂崩壊剤を撹拌機
から取り出して、常温下で拡散して放置するか、
送風機を用いてゆるやかな風で冷却してもよく冷
風を用いて強制冷却してもよい。消臭剤は防水加
工を施してないものも使用することが出来る。こ
の場合は粉、粒状のワツクス又は粉、粒状の低分
子量ポリオレフイン樹脂等の内の1種又は2種以
上と消臭剤の内の1種又は2種以上を混合したも
のを鋳型砂に添加するか、又は鋳型砂に粉、粒状
のワツクス又は粉、粒状の低分子量ポリオレフイ
ン樹脂等の内の1種又は2種以上と消臭剤の内の
1種又は2種以上を同時に添加して撹拌する。消
臭剤に防水加工を施してない鋳型砂崩壊剤を添加
混練した鋳型砂は、粉、粒状のワツクス又は粉、
粒状の低分子量ポリオレフイン樹脂等の内の1種
又は2種以上と消臭剤の内の1種又は2種以上と
の混合比が同一の場合、防水加工を施した消臭剤
を使用した鋳型砂崩壊剤より消臭効果は劣り、混
練砂の可使用時間も短くなるが、鋳型砂の混練は
連続混練機を使用すれば、可使用時間が短かくて
も鋳型の成型は容易に出来る。 次に本発明の鋳型砂崩壊剤の崩壊性を実施例に
より説明する。この測定に使用した試料はJIS所
定の50φ×50長さのものを用い、測定内容は表面
安定性試験、常温強度試験、各加熱温度における
残留強度試験を行ない、その結果は第1表及び第
2表に示す。又これに使用した鋳型砂崩壊剤の配
合は、 鋳型砂崩壊剤―1 粉、粒状の石油系ワツクス100重量部と粉、粒
状のフアーネスカーボン45重量部との混合物。 鋳型砂崩壊剤―2 粉、粒状の石油系ワツクス100重量部と粉、粒
状のチヤンネルカーボン45重量部との混合物。 鋳型砂崩壊剤―3 粉、粒状の石油系ワツクス100重量部と木粉45
重量部との混合物。 鋳型砂崩壊剤―4 粉、粒状の石油系ワツクス100重量部と籾殻の
粉、粒状の粉砕物45重量部との混合物。 鋳型砂崩壊剤―5 粉、粒状の石油系ワツクス100重量部と米の
粉、粒状の粉砕物45重量部との混合物。 鋳型砂崩壊剤―6 粉、粒状の石油系ワツクス100重量部と粉、粒
状の澱粉45重量部との混合物。 鋳型砂崩壊剤―7 粉、粒状の植物系ワツクス(カルナウバワツク
ス)100重量部と木粉45重量部との混合物。 鋳型砂崩壊剤―8 粉、粒状の植物系ワツクス(綿ワツクス)100
重量部と木粉45重量部との混合物。 鋳型砂崩壊剤―9 粉、粒状の動物系ワツクス(ミツワツクス)
100重量部と木粉45重量部との混合物。 鋳型砂崩壊剤―10 粉、粒状の動物系ワツクス(羊毛ワツクス)
100重量部と木粉45重量部との混合物。 鋳型砂崩壊剤―11 粉、粒状の低分子量ポリオレフイン樹脂100重
量部と木粉45重量部との混合物。 鋳型砂崩壊剤―12 粉、粒状のアタクチツクポリプロピレン樹脂
100重量部と木粉45重量部との混合物。 鋳型砂崩壊剤―13 粉、粒状の化学構造不明の所謂釜残樹脂状物
100重量部と木粉45重量部との混合物。 実施例 1 自硬性鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―1 1.2重量部 水ガラス(モル比2.5、42B―) 6重量部 硬化剤(ダイカル粉) 2重量部 実施例 2 自硬性鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―2 1.2重量部 水ガラス(モル比2.5、42B―) 6重量部 硬化剤(ダイカル粉) 2重量部 実施例 3 自硬性鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―3 1.2重量部 水ガラス(モル比2.5、42B―) 6重量部 硬化剤(ダイカル粉) 2重量部 実施例 4 自硬性鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―4 1.2重量部 水ガラス(モル比2.5、42B―) 6重量部 硬化剤(ダイカル粉) 2重量部 実施例 5 自硬性鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―5 1.2重量部 水ガラス(モル比2.5、42B―) 6重量部 硬化剤(ダイカル粉) 2重量部 実施例 6 自硬性鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―6 1.2重量部 水ガラス(モル比2.5、42B―) 6重量部 硬化剤(ダイカル粉) 2重量部 実施例 7 自硬性鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―7 1.2重量部 水ガラス(モル比2.5、42―) 6重量部 硬化剤(ダイカル粉) 2重量部 実施例 8 自硬性鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―8 1.2重量部 水ガラス(モル比2.5、42―) 6重量部 硬化剤(ダイカル粉) 2重量部 実施例 9 自硬性鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―9 1.2重量部 水ガラス(モル比2.5、42―) 6重量部 硬化剤(ダイカル粉) 2重量部 実施例 10 自硬性鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―10 1.2重量部 水ガラス(モル比2.5、42―) 6重量部 硬化剤(ダイカル粉) 2重量部 実施例 11 自硬性鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―11 1.2重量部 水ガラス(モル比2.5、42―) 6重量部 硬化剤(ダイカル粉) 2重量部 実施例 12 自硬性鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―12 1.2重量部 水ガラス(モル比2.5、42―) 6重量部 硬化剤(ダイカル粉) 2重量部 実施例 13 自硬性鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―13 1.2重量部 水ガラス(モル比2.5、42―) 6重量部 硬化剤(ダイカル粉) 2重量部 実施例1〜実施例13は試料を採取成型して常温
下で放置して硬化完了後測定を行なつた。 実施例 14 CO2ガス鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―1 1.2重量部 水ガラス(モル比2.3、50―) 6重量部 実施例 15 CO2ガス鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―3 1.2重量部 水ガラス(モル比2.3、50―) 6重量部 実施例 16 CO2ガス鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―8 1.2重量部 水ガラス(モル比2.3、50―) 6重量部 実施例 17 CO2ガス鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―10 1.2重量部 ガラス(モル比2.3、50―) 6重量部 実施例 18 CO2ガス鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―11 1.2重量部 水ガラス(モル比2.3、50―) 6重量部 実施例14〜実施例18は試料を採取成型後CO2
スを30秒間通して硬化させた後測定を行なつた。 実施例 19 セメント鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―1 1.2重量部 ポルトランドセメント 8重量部 水 8重量部 実施例 20 セメント鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―3 1.2重量部 ポルトランドセメント 8重量部 水 8重量部 実施例 21 セメント鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―8 1.2重量部 ポルトランドセメント 8重量部 水 8重量部 実施例 22 セメント鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―10 1.2重量部 ポルトランドセメント 8重量部 水 8重量部 実施例 23 セメント鋳型砂 けい砂(鋳物用6号) 100重量部 鋳型砂崩壊剤―11 1.2重量部 ポルトランドセメント 8重量部 水 8重量部 実施例19〜実施例23は試料を採取成型して常温
下で放置して硬化完了後測定を行なつた。
The present invention relates to an improved mold sand disintegrator. Water glass molds and cement molds are extremely popular in casting manufacturing because they are easy to mold and the material costs are low. After the sand has solidified and the mold is destroyed to take out the product, the molding sand has poor collapsibility and it takes time to remove the sand, which requires a pneumatic hammer, a large hammer, etc. This causes worker fatigue and requires a great deal of effort, and the impact of the hammer can cause cracks in the casting, resulting in defective products, which sometimes impedes productivity. This is the biggest drawback of water glass-based molds and cement-based molds. has been used as a disintegrant, but no significant results have been obtained in terms of improving disintegration. This is because if a large amount of powder disintegrants such as wood flour are used, the disintegration properties will improve, but as the surface area of the powder increases, the binding force of the binder water glass and cement will decrease, and the strength of the mold at room temperature will decrease. It becomes weak and the surface stability of the mold is poor, making it difficult to handle. Water-soluble auxiliary binders such as sucrose are dissolved in the water contained in the water glass, increasing the binding power of the sand, reducing the fluidity of the sand, and making molding time-consuming. In addition, water glass absorbs water into the water-soluble auxiliary binder, so the kneaded sand dries quickly and the usable life of the sand is shortened, and in the case of CO 2 gas type sand, the kneaded sand cannot be stored. In the case of cement molds, molasses is used, but the sand generates heat, which causes a lot of wear and tear on the wooden mold (the model used to make the mold) and produces an unpleasant odor. When sucrose and glucose become liquid sugar, their effectiveness as disintegrants decreases.Disintegrants that absorb water during or after the mixing of molding sand are difficult to dehydrate, and due to the residual water, the strength of the mold decreases and the surface of the mold deteriorates. Stability also deteriorates. Therefore, sucrose, glucose, starch, etc. are scattered in the form of powder or granules between the grains of sand in the mold, and when poured, they are heated by hot water, burnt, and carbonized, and are generated during the process of solidifying the casting. It exerts a buffering effect by absorbing compressive force, but when dissolved in water, this buffering effect decreases, causing the molding sand to tighten and become less collapsible. Especially the core (the inner mold of the casting)
This tendency is strong. Furthermore, molds using water-soluble auxiliary binders are hygroscopic, and if the molds are not sufficiently dried, gas defects will occur in the castings. Up until now, using too many disintegrants has improved disintegration, but it has also increased material costs, deteriorated mold strength and surface stability, and increased gas generation due to combustion of combustible materials during pouring, resulting in castings with gas defects. Many defects occur due to Traditionally, water glass-based molding sand and cement-based molding sand were disposable because they were cheap, but as regulations on industrial waste disposal became stricter, the cost of waste disposal became a larger proportion of the manufacturing cost of castings. As the recovery and recycling of sand has become an urgent need, recycling equipment has become widely installed. However, with poorly collapsible sand, a lot of hardened binder sticks to the surface of the sand grains, and the sand grains are tightly bound together, forming large sand blocks. This takes a lot of time and effort, such as crushing it using a crusher and removing foreign matter stuck to the surface of the sand grains using a sand grain polisher, but the sand grains are crushed and the recovery rate is poor. It is treated as industrial waste. Powder, granular petroleum-based wax, powder, granular plant-based wax, powder, granular animal-based wax (hereinafter, the above various waxes may be collectively referred to as powder or granular wax),
Powder, granular low molecular weight polyolefin resin, powder, granular atactic polypropylene resin, powder, granular chemical structure unknown so-called kettle residue resin (hereinafter, the above various resins and resin-like substances are collectively referred to as powder, granular polyolefin) Molding sand disintegrants consisting of one or more types of resins (sometimes expressed as resins, etc.) exhibit remarkable disintegrability and have a high rate of sand reuse, but because they are soft, they are crushed during kneading. It adheres to the kneading machine and softens in the summer or at high temperatures in the workplace, making it difficult to handle, and it also burns during pouring, creating an unpleasant odor, which makes the working environment worse. The present invention uses powders, granular petroleum waxes, powders, granular vegetable waxes, powders, granular animal waxes, powders, granular low molecular weight polyolefin resins, powders, granular Atactic polypropylene resin, powder, granular chemical structure unknown so-called kettle residue resin material to increase the hardness and use as an unpleasant odor deodorizer powder, granular graphite, wood powder, rice husk powder, granular crushed material, Grain flour, ground granules,
One or more types of powder and granular starch (hereinafter, the above various deodorants may be collectively referred to as deodorants) are added and mixed. The features of the present invention include powder, granular petroleum wax, powder, granular vegetable wax, powder, granular animal wax, powder, granular low molecular weight polyolefin resin, powder, granular atactic polypropylene resin, Powder, granular graphite, wood flour, rice husk powder, granular pulverized product, grain powder, granular pulverized product, powder A deodorizing agent made of one or more types of granular starch is coated on the surface to form a waterproof coating and then added to water glass molding sand or cement molding sand. The newly developed molding sand with the addition of a molding sand disintegrant has improved sand fluidity, reduces the work of pounding and hardening the molding sand, and makes molding easier.
In addition, since the water-absorbing substance is waterproofed, it does not adsorb the moisture required for the binder, so the usable life of the kneaded sand is long, and the surface stability of the mold at room temperature is also good, making it easier to use water glass-based molding sand. In some cases, the amount of water glass added can be smaller than that of conventional water glass molding sand. The mold sand disintegrating agent, which is scattered between the sand grains, is heated by high-temperature water during pouring and melts and dissolves before the mold sand expands, and its fluidity is extremely good, allowing it to flow out and disperse widely in the gaps between the sand grains. However, especially in the case of water glass-based molding sand, before the hardened water glass is softened under high temperature and pressure, a carbonized film is formed on the surface of the sand grains and the binder to prevent the binder from sticking. Small cavities are formed in the area where this mold sand disintegrator dissolves, making the mold porous and acting as a buffer for the sand that expands with the temperature of the water and the compressive force generated during the solidification process of the casting. Absorbs and prevents mold destruction.
The greater the amount of residual heat after casting, the wider the range of carbonization in which the mold sand disintegrator elutes, and the mold exhibits extremely remarkable collapsibility. The deodorant is dispersed and dotted between the sand grains, and when poured, it is heated with high-temperature water, and all substances other than graphite are carbonized. This carbide acts as a buffer material that absorbs the sand that expands with the temperature of the water and the compressive force generated during the solidification process of castings, and not only has an auxiliary effect on improving collapsibility, but also acts as a material for powder, granular wax, and powder. The unpleasant odor that occurs when granular low-molecular-weight polyolefin resins are burned is caused by the addition of deodorizing agents, which increases the melting point and causes the combustion temperature to shift to a higher temperature side, resulting in high-temperature combustion. This deodorizing effect plays an important role in improving the working environment. To explain the present invention in more detail, powder added as a deodorant, granular graphite, wood flour, rice husk powder, granular pulverized product, grain powder, granular pulverized product,
Powder, granular petroleum-based wax, powder, granular vegetable-based wax,
Powder, granular animal wax, powder, granular low molecular weight polyolefin resin, powder, granular atactic polypropylene resin, powder, granular one or more of so-called kettle residue resin-like substances of unknown chemical structure, 5 to 5 The amount is preferably within 100 parts by weight.This deodorant is waterproofed using a Henschel mixer.The Henschel mixer is equipped with a jacket for cooling water on the outer wall of the stirring section, and powder, granular wax, or powder,
When 100 parts by weight of one or more granular low molecular weight polyolefin resins and 5 to 100 parts by weight of one or more deodorants are simultaneously added and stirred, the mixture is mixed. The powder, granular wax, powder, granular low molecular weight polyolefin resin, etc. and the deodorant heat up to around 50℃ due to friction, and this heat causes the powder, granular wax, powder, granular low molecular weight polyolefin resin, etc. Molecular weight polyolefin resin and the like soften and adhere to the surface of the deodorant to form a waterproof coating. The deodorizer coated with a waterproof coating is fed into the cooling water jacket of the Henschel mixer and cooled while stirring, and the powder, granular wax, powder, granular low molecular weight polyolefin resin, etc. and the deodorant solidify. It is possible to obtain a mold sand disintegrating agent with good fluidity by preventing the deodorizing agent's waterproof coating from peeling off. This waterproof stirrer is not limited to Henschel mixers;
The powder, granular wax, powder, granular low molecular weight polyolefin resin, etc. will not be crushed or crushed, and the powder, granular wax, powder, granular low molecular weight polyolefin resin, etc. will not be crushed or crushed by frictional heat. Any type of stirrer may be used as long as it does not melt, and cooling may not require the use of cooling water. In this case, take out the mold sand disintegrator that has been waterproofed from the stirrer and leave it to disperse at room temperature, or
Cooling may be performed by gentle wind using a blower, or forced cooling may be performed using cold air. Deodorants can be used even if they are not waterproof. In this case, a mixture of powder, granular wax, powder, granular low molecular weight polyolefin resin, etc., and one or more deodorizers is added to the molding sand. Alternatively, one or more of powder, granular wax or powder, granular low-molecular-weight polyolefin resin, etc. and one or more of deodorants are simultaneously added to the molding sand and stirred. . Mold sand made by adding and kneading a mold sand disintegrant without waterproofing to a deodorizer is powder, granular wax or powder,
If the mixing ratio of one or more of the granular low molecular weight polyolefin resins, etc. and one or more of the deodorants is the same, molds using waterproofed deodorizers Although the deodorizing effect is inferior to that of sand disintegrants, and the usable life of the kneaded sand is shortened, if a continuous kneader is used to knead the molding sand, molds can be easily formed even if the usable time is short. Next, the disintegrating properties of the mold sand disintegrating agent of the present invention will be explained using examples. The sample used for this measurement was a JIS-specified 50φ x 50 length, and the measurements included a surface stability test, room temperature strength test, and residual strength test at each heating temperature.The results are shown in Table 1 and It is shown in Table 2. The composition of the mold sand disintegrant used here is: Mold sand disintegrator-1 A mixture of 100 parts by weight of powdered or granular petroleum wax and 45 parts by weight of powdered or granular furnace carbon. Mold sand disintegrant - 2 A mixture of 100 parts by weight of powdered or granular petroleum wax and 45 parts by weight of powdered or granular channel carbon. Mold sand disintegrant - 3 100 parts by weight of powdered or granular petroleum wax and 45 parts by weight of wood powder
Mixture with parts by weight. Mold sand disintegrator-4 A mixture of 100 parts by weight of powdered or granular petroleum-based wax and 45 parts by weight of rice husk powder or pulverized granules. Mold sand disintegrant - 5 A mixture of 100 parts by weight of powdered or granular petroleum-based wax and 45 parts by weight of rice flour or granular crushed material. Mold sand disintegrant - 6 A mixture of 100 parts by weight of powdered or granular petroleum wax and 45 parts by weight of powdered or granular starch. Mold sand disintegrant - 7 A mixture of 100 parts by weight of powdered or granular vegetable wax (carnauba wax) and 45 parts by weight of wood flour. Mold sand disintegrant - 8 Powder, granular vegetable wax (cotton wax) 100
A mixture of parts by weight and 45 parts by weight of wood flour. Mold sand disintegrant - 9 Powder, granular animal wax (Mitsuwa wax)
A mixture of 100 parts by weight and 45 parts by weight of wood flour. Mold sand disintegrant - 10 Powder, granular animal wax (wool wax)
A mixture of 100 parts by weight and 45 parts by weight of wood flour. Mold sand disintegrant - 11 A mixture of 100 parts by weight of powder or granular low molecular weight polyolefin resin and 45 parts by weight of wood flour. Mold sand disintegrant - 12 Powder, granular atactic polypropylene resin
A mixture of 100 parts by weight and 45 parts by weight of wood flour. Mold sand disintegrant - 13 Powder, granular, so-called pot residue resinous material with unknown chemical structure
A mixture of 100 parts by weight and 45 parts by weight of wood flour. Example 1 Self-hardening mold sand Silica sand (No. 6 for foundries) 100 parts by weight Molding sand disintegrant-1 1.2 parts by weight Water glass (molar ratio 2.5, 42B- e ) 6 parts by weight Hardening agent (Dical powder) 2 parts by weight Example 2 Self-hardening mold sand Silica sand (No. 6 for foundries) 100 parts by weight Molding sand disintegrant-2 1.2 parts by weight Water glass (molar ratio 2.5, 42B- e ) 6 parts by weight Hardening agent (Dical powder) 2 parts by weight Example 3 Self-hardening mold sand Silica sand (No. 6 for foundries) 100 parts by weight Molding sand disintegrant-3 1.2 parts by weight Water glass (molar ratio 2.5, 42B- e ) 6 parts by weight Hardening agent (Dical powder) 2 parts by weight Example 4 Self-hardening mold sand Silica sand (No. 6 for foundries) 100 parts by weight Molding sand disintegrant-4 1.2 parts by weight Water glass (molar ratio 2.5, 42B- e ) 6 parts by weight Hardening agent (Dical powder) 2 parts by weight Example 5 Self-hardening mold sand Silica sand (No. 6 for foundries) 100 parts by weight Molding sand disintegrant-5 1.2 parts by weight Water glass (molar ratio 2.5, 42B- e ) 6 parts by weight Hardening agent (Dical powder) 2 parts by weight Example 6 Self-hardening mold sand Silica sand (No. 6 for foundries) 100 parts by weight Molding sand disintegrant-6 1.2 parts by weight Water glass (molar ratio 2.5, 42B- e ) 6 parts by weight Hardening agent (Dical powder) 2 parts by weight Example 7 Self-hardening mold sand Silica sand (No. 6 for foundries) 100 parts by weight Molding sand disintegrant-7 1.2 parts by weight Water glass (molar ratio 2.5, 42- e ) 6 parts by weight Hardening agent (Dical powder) 2 parts by weight Example 8 Self-hardening mold sand Silica sand (No. 6 for foundries) 100 parts by weight Molding sand disintegrant-8 1.2 parts by weight Water glass (molar ratio 2.5, 42- e ) 6 parts by weight Hardening agent (Dical powder) 2 parts by weight Example 9 Self-hardening mold sand Silica sand (No. 6 for foundries) 100 parts by weight Molding sand disintegrant-9 1.2 parts by weight Water glass (molar ratio 2.5, 42- e ) 6 parts by weight Hardening agent (Dical powder) 2 parts by weight Example 10 Self-hardening mold sand Silica sand (No. 6 for foundries) 100 parts by weight Molding sand disintegrant-10 1.2 parts by weight Water glass (molar ratio 2.5, 42- e ) 6 parts by weight Hardening agent (Dical powder) 2 parts by weight Example 11 Self-hardening mold sand Silica sand (No. 6 for foundries) 100 parts by weight Molding sand disintegrant-11 1.2 parts by weight Water glass (molar ratio 2.5, 42- e ) 6 parts by weight Hardening agent (Dical powder) 2 parts by weight Example 12 Self-hardening mold sand Silica sand (No. 6 for foundries) 100 parts by weight Molding sand disintegrant-12 1.2 parts by weight Water glass (molar ratio 2.5, 42- e ) 6 parts by weight Hardening agent (Dical powder) 2 parts by weight Example 13 Self-hardening mold sand Silica sand (No. 6 for foundries) 100 parts by weight Molding sand disintegrant-13 1.2 parts by weight Water glass (molar ratio 2.5, 42- e ) 6 parts by weight Hardening agent (Dical powder) 2 parts by weight In Examples 1 to 13, samples were collected, molded, left at room temperature, and measured after curing was completed. Example 14 CO 2 gas molding sand Silica sand (No. 6 for foundries) 100 parts by weight Molding sand disintegrant-1 1.2 parts by weight Water glass (molar ratio 2.3, 50- e ) 6 parts by weight Example 15 CO 2 gas molding sand Silica sand (No. 6 for foundries) 100 parts by weight Molding sand disintegrator-3 1.2 parts by weight Water glass (molar ratio 2.3, 50- e ) 6 parts by weight Example 16 CO 2 gas molding sand Silica sand (No. 6 for foundries) 100 parts by weight Mold sand disintegrant - 8 1.2 parts by weight Water glass (molar ratio 2.3, 50 - e ) 6 parts by weight Example 17 CO 2 gas mold sand silica sand (No. 6 for foundries) 100 parts by weight Mold sand disintegrant - 10 1.2 parts by weight Glass (molar ratio 2.3, 50- e ) 6 parts by weight Example 18 CO 2 gas mold sand silica sand (No. 6 for foundries) 100 parts by weight Molding sand disintegrant - 11 1.2 parts by weight Water glass (molar ratio 2.3, 50- e ) 6 parts by weight In Examples 14 to 18, samples were collected, molded, and then cured by passing CO 2 gas through them for 30 seconds before measurement. Example 19 Cement molding sand silica sand (No. 6 for foundry use) 100 parts by weight Molding sand disintegrant-1 1.2 parts by weight Portland cement 8 parts by weight Water 8 parts by weight Example 20 Cement molding sand silica sand (No. 6 for foundry use) 100 Parts by weight Mold sand disintegrant - 3 1.2 parts by weight Portland cement 8 parts by weight Water 8 parts by weight Example 21 Cement mold sand silica sand (No. 6 for foundries) 100 parts by weight Mold sand disintegrant - 8 1.2 parts by weight Portland cement 8 parts by weight Part water 8 parts by weight Example 22 Cement molding sand silica sand (No. 6 for casting) 100 parts by weight Molding sand disintegrant - 10 1.2 parts by weight Portland cement 8 parts by weight Water 8 parts by weight Example 23 Cement molding sand silica sand (for casting 6) 100 parts by weight Mold sand disintegrant - 11 1.2 parts by weight Portland cement 8 parts by weight Water 8 parts by weight In Examples 19 to 23, samples were collected, molded, left at room temperature, and measured after hardening was completed. I did it.

【表】 表面安定性の測定は、鋳物砂ふるい分け機(ロ
タツプ型)に試料を入れて篩上で2分間振動し、
測定前試料重量と測定後試料重量の比を%で表わ
した。
[Table] To measure the surface stability, place the sample in a foundry sand sieve (rotap type) and vibrate it on the sieve for 2 minutes.
The ratio of the sample weight before measurement to the sample weight after measurement was expressed in %.

【表】 第2表中従来の自硬性鋳型砂及びセメント鋳型
砂の配合は下記の通りである。 自硬性鋳型砂 けい砂(鋳物用6号) 100重量部 水ガラス(モル比2.5、42B―) 6重量部 硬化剤(ダイカル粉) 2重量部 セメント鋳型砂 けい砂(鋳物用6号) 100重量部 ポルトランドセメント 8重量部 ピーチコークス粉 1.5重量部 水 8重量部 従来の自硬性鋳型砂やセメント鋳型砂の残留強
度に比較して、1100℃における本発明の実施例1
〜23の残留強度は極めて低く優れている。又この
鋳型砂崩壊剤―1〜13は、けい砂に限らずオリビ
ンサンド、ジルコンサンドえの添加も可能で、そ
れに使用する粘結剤の水ガラスはCO2ガス鋳型砂
用低モル比水ガラスから高モル比水ガラスまで
と、結合剤のセメントは普通ポルトランドセメン
トから超早強ポルトランドセメントまでの使用が
可能である。 以上のように本発明の鋳型砂崩壊剤は鋳型砂に
添加するだけでその鋳型の崩壊性を良好にする。
この鋳型砂崩壊剤使用に際しては砂の混練設備や
鋳型成型方法等従来の水ガラス系鋳型法やセメン
ト系鋳型法と全く変ることなく、砂の管理及び取
り扱いも容易である。この新しい鋳型砂崩壊剤の
使用によつて吸湿性がなく、成型も容易で放置後
の常温強度及び表面安定性も良好で、可燃物の燃
焼により発生するガスによる鋳物の欠陥をともな
はない鋳型砂で鋳造された鋳物は、砂落し作業に
おいて極めて顕著な崩壊性を発揮し、作業が迅速
に進展して生産性が向上し、作業者の疲労の度合
も僅少である。本発明の鋳型砂崩壊剤に添加され
る消臭剤の中には産業廃棄物として処理されるも
のもあり、その再生利用の向上とあいまつて省資
源効果も大きく、本発明によつて崩壊性の極めて
優秀な鋳型砂崩壊剤の提供により、鋳造業界に多
大の利益をもたらすことが出来る。
[Table] The compositions of conventional self-hardening molding sand and cement molding sand in Table 2 are as follows. Self-hardening molding sand Silica sand (No. 6 for foundry use) 100 parts by weight Water glass (molar ratio 2.5, 42B- e ) 6 parts by weight Hardening agent (Dical powder) 2 parts by weight Cement molding sand Silica sand (No. 6 for foundry use) 100 Parts by weight Portland cement 8 parts by weight Peach coke powder 1.5 parts by weight Water 8 parts by weight Compared to the residual strength of conventional self-hardening molding sand and cement molding sand, Example 1 of the present invention at 1100°C
The residual strength of ~23 is extremely low and excellent. In addition, these molding sand disintegrants 1 to 13 are not limited to silica sand, but can also include olivine sand and zircon sand, and the water glass used as a binder is a low molar ratio water glass for CO 2 gas molding sand. to high molar ratio water glass, and binder cements ranging from ordinary Portland cement to ultra-early strength Portland cement can be used. As described above, the mold sand disintegrant of the present invention improves the disintegrability of the mold simply by adding it to mold sand.
When using this mold sand disintegrant, the sand kneading equipment and mold forming method are completely unchanged from the conventional water glass molding method or cement molding method, and the management and handling of the sand is easy. By using this new mold sand disintegrant, there is no hygroscopicity, easy molding, good strength at room temperature and surface stability after storage, and there are no defects in castings caused by gases generated by combustion of combustible materials. Castings cast with molding sand exhibit extremely remarkable collapsibility during sand removal work, the work progresses quickly, productivity is improved, and the degree of worker fatigue is minimal. Some of the deodorants added to the molding sand disintegrating agent of the present invention are treated as industrial waste, and together with the improvement of their recycling, the resource saving effect is also significant. By providing an extremely excellent mold sand disintegrator, the foundry industry can bring great benefits.

Claims (1)

【特許請求の範囲】[Claims] 1 粉、粒状の黒鉛、木粉、籾殻の粉、粒状の粉
砕物、穀類の粉、粒状の粉砕物、粉、粒状の澱粉
の1種又は2種以上5〜100重量部を、粉、粒状
の石油系ワツクス、粉、粒状の植物系ワツクス、
粉、粒状の動物系ワツクス、粉、粒状の低分子量
ポリオレフイン樹脂、粉、粒状のアタクチツクポ
リプロピレン樹脂の1種又は2種以上100重量部
で表面処理してなる鋳型砂崩壊剤。
1. 5 to 100 parts by weight of one or more of powder, granular graphite, wood flour, rice husk powder, pulverized granules, grain powder, pulverized granules, flour, and granular starch, into powder, granular petroleum-based wax, powder, granular vegetable-based wax,
A mold sand disintegrator obtained by surface treatment with 100 parts by weight of one or more of powdered or granular animal wax, powdered or granular low molecular weight polyolefin resin, or powdered or granular atactic polypropylene resin.
JP10217579A 1979-08-13 1979-08-13 Mold sand collapsing agent Granted JPS5626654A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10217579A JPS5626654A (en) 1979-08-13 1979-08-13 Mold sand collapsing agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10217579A JPS5626654A (en) 1979-08-13 1979-08-13 Mold sand collapsing agent

Publications (2)

Publication Number Publication Date
JPS5626654A JPS5626654A (en) 1981-03-14
JPS6230063B2 true JPS6230063B2 (en) 1987-06-30

Family

ID=14320342

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10217579A Granted JPS5626654A (en) 1979-08-13 1979-08-13 Mold sand collapsing agent

Country Status (1)

Country Link
JP (1) JPS5626654A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5711744A (en) * 1980-06-26 1982-01-21 Hatano Yoshiyo Molding sand collapsing agent
JPS63177939A (en) * 1987-01-17 1988-07-22 Idemitsu Kosan Co Ltd Additive for casting sand mold

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4920455A (en) * 1972-06-20 1974-02-22

Also Published As

Publication number Publication date
JPS5626654A (en) 1981-03-14

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