JPS5961546A - Binder material for casting mold curable by hot wind - Google Patents
Binder material for casting mold curable by hot windInfo
- Publication number
- JPS5961546A JPS5961546A JP17052482A JP17052482A JPS5961546A JP S5961546 A JPS5961546 A JP S5961546A JP 17052482 A JP17052482 A JP 17052482A JP 17052482 A JP17052482 A JP 17052482A JP S5961546 A JPS5961546 A JP S5961546A
- Authority
- JP
- Japan
- Prior art keywords
- mold
- casting mold
- resin
- hot wind
- binder material
- 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
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
- B22C1/16—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents
- B22C1/20—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents
- B22C1/22—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents of resins or rosins
- B22C1/2233—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents of resins or rosins obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- B22C1/226—Polyepoxides
-
- 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
- B22C1/16—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents
- B22C1/20—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents
- B22C1/22—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents of resins or rosins
- B22C1/2233—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents of resins or rosins obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- B22C1/2246—Condensation polymers of aldehydes and ketones
- B22C1/2253—Condensation polymers of aldehydes and ketones with phenols
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Mold Materials And Core Materials (AREA)
Abstract
Description
【発明の詳細な説明】
本舶明は幼規lシ゛1型の襄嚢方法に用いろ11ゐ饅風
硬化性υJ型用粘桁拐科Vこ関1゛る。DETAILED DESCRIPTION OF THE INVENTION The present invention has a 11-year-old steam-hardening υJ-type viscous frame removal method that can be used for the sac method of the 1st type.
従来から水力ラス(珪酸ソーダ)を炭酸ガスで仮;化さ
ぜるものか広く使わ7している。こ11け。Traditionally, hydraulic lath (sodium silicate) has been widely used as a method of temporarily oxidizing it with carbon dioxide gas. This is 11.
力1」熱の必νかないこと、戻敵カス吹き込み後。Power 1: There is no need for heat, and after blowing back enemy dregs.
的ちに抜型−(さゐなどの利点ケもっていめ。しかし、
粘粕駒科か無僚物−Cあるため炉焼性がlく駒造波の1
.1型り崩截性刀3悪く又多αF時には釣型會放置する
こと(/!−より、強1貌が低下するという欠点會廟し
ている。水ガラス−炭酸ガス法の鋳型の崩壊性を改良す
るため、水力ラスにデキス) l)ン、木粉、せfi!
j、樹脂などを冷加した粘粕拐科か11茶さ71てい、
6が、cILらはいず1′1−も水ガラスリ皿甘を阻害
し、粘結力全低下さゼ注陽後の鋳型の崩敵性改善を鋳型
強IWケ両立させるのに十分とけばえなかった。Take advantage of cutting dies and other benefits. However,
Komazoha's 1 has low kiln-firing properties due to the presence of lees-komaceae or infidels-C.
.. 1 mold has a disadvantage of deterioration, and in the case of multi-αF, the strength of the sword is reduced. In order to improve the hydraulic lath) l) N, wood powder, sefi!
j, 11-tea 71-tei, which is made by cooling resin etc.
6, cIL et al. 1'1- also inhibit water glazing, completely reduce the caking force, and are not sufficient to improve mold collapsibility after injection and strengthen mold IW. Ta.
一方M磯物紮粘粕材料としたも(lJにフェノール樹脂
を使用し加熱して鋳型とするシールモールド法鋳型や、
2ラン樹刀旨會酸で硬化さぜゐ自硬性鋳型が卸らnて2
r)鋳型の崩壊性に勝Iしているが、カロ熱會心安とし
πり、常編で固化する1でに長時lt+]かかるなどの
欠点ケもっている。On the other hand, there are molds made from M rock lees (seal mold molds that use phenolic resin for lJ and heat them to form molds,
A self-hardening mold that hardens with 2-run synthetic acid is released.
r) Although it is superior to the disintegrability of the mold, it has drawbacks such as being unstable in heating and requiring a long time to solidify in a regular process.
又、フェノール樹脂とインシア不−)f王枯結材とし、
アミンガスを吹き込む乙とにエリ室硯で直ちに硬化抜型
できる鋳型用枯幀材料が開発さILπが使用するアミ/
ガス(/J毒性や英気り対策に問題がある。In addition, phenolic resin and insea non-)f king-bearing material are used,
In addition to blowing amine gas, a dry material for molds that can be immediately hardened and cut out with an inkstone was developed.
Gas (/JThere are problems with toxicity and energy measures.
不発明は上記欠点會改筈丁/8目的でlきfL7ζもの
で4f機物ケ王安粘結材として用い褥性(/J7iい熱
風ケ吹き込んで直ちに抜型でき注湯後の崩壊性がMr+
かつ多湿時の鋳型強度を改善した鋳型金与える鋳型用粘
結材料全提供丁ゐものでめる0
不発明Ha) フェノール性樹脂とb)水とC)アル
カリ金属の水酸化物とd)エポキシ樹脂とe)必をvこ
応じ°Cアルコール類からなる熱風硬化性@型狗科に関
し、cnと耐火物粒子からなる鋳型用組成物lグ毒性の
ない空気ケ加黙した熱Kを吹き込んで硬化させることか
出さ直ちに抜型i3J酢となる0史VC放直により側)
Jhの硬化反応か進み多湿時の防型強度低下を改舌した
鋳型ケ製珀する0とができ^0又王粘結材は有伎物であ
り注尚俊C/J鉤型り崩壊性も優r1ている。The non-invention is that the above-mentioned disadvantages can be modified for the purpose of /8, and it is used as a binder for 4f machines.
We also provide a complete set of bonding materials for molds that provide molds with improved mold strength in high humidity conditions. Regarding hot air curable @ molds made of resin and e) required °C alcohols, mold compositions made of cn and refractory particles were blown with non-toxic air and silenced heat K. After hardening, the cutting mold becomes i3J vinegar as soon as the VC is left undisturbed)
As the hardening reaction of Jh progresses, it is possible to make a mold that improves the deterioration of the mold proofing strength in high humidity conditions.In addition, the King's caking material is a unique material and has the same disintegration properties as the C/J hook shape. There is a good r1.
硬化CLJ1か構1′I熱風ヶ吹き込むことによI2.
(+)粘結材中の水分が除去さIL粘結材がp〜枯し固
化す/、J。(2)史に鋳型會放直う−ゐことにエリフ
ェノール1生水酸基とエポキシ但j脂中すエボキシ基が
粘鯖制中のアルカリ金属の触媒作用[L、lj硬化反応
が進み鋳)(す強度全向上させ7:Iりめと考えらfL
る。Harden CLJ1 by blowing hot air into the structure I2.
(+) Moisture in the caking agent is removed and the IL caking agent dries up and solidifies/, J. (2) When the molding process is resumed, the catalytic action of the alkali metals during the viscosity control [L, lj hardening reaction progresses and the casting process] is caused by the hydroxyl groups of Eliphenol 1 and the epoxy groups in the epoxy resin. Totally improves strength 7: I think fL
Ru.
本発明で用いらnるフェノール性412(脂とじてにい
わゆるフェノールホルムアルデヒド糸柄脂だけでなくフ
ニノール笈性キシレン位1月β、フェノール変性トルエ
ン初脂、カシュー樹脂、 DFK(頁岩曲)樹脂°など
そ(/、J高分子骨格の中に多価金属と増を形欲し、エ
ポキシ〃;と反応丁ゐ)、ノール性水酸基をもつでいる
樹脂であt′Lはよい。The phenolic 412 used in the present invention includes not only so-called phenol-formaldehyde thread fat, but also phenol-based xylene-based fat, phenol-modified toluene fat, cashew resin, DFK (shale bend) resin, etc. Therefore, t'L is good for resins that have a norlic hydroxyl group in the J polymer skeleton and react with epoxy.
又フェノール性樹脂にレゾール型、ノボラック型、Nメ
チレン型レゾール、ジメチレンエーテル型レゾール、ホ
ルマー/L/型しゾール等樹脂し/J結せ形式に曲伸l
〈不目的に使用丁ゐことかで酢、−ml 脂台成原料で
あるフェノールiVこついてもフェノールたけてl〈ク
レゾール、ブチルフェノール、ビスフェノール、ノニル
フェノール、カテコール、レゾルシノール7CトW 用
丁なことができる。In addition, resins such as resol type, novolak type, N-methylene type resol, dimethylene ether type resol, Former/L/type sol etc. are applied to phenolic resins, and bending and stretching are applied to the J-binding type.
(Vinegar used for unintended purposes, -ml) Phenol iV, which is a raw material for making fats, does not contain phenol (cresol, butylphenol, bisphenol, nonylphenol, catechol, resorcinol 7C) .
アルデヒド類についてもホルマリン、パラホルム、ヘキ
サミン、アセトアルテヒドなどが使用でさゐ〇
水はフェノール性4111脂及びアルカリ金属の水酸化
物が耐火物粒子へ均一に被保さnるπめに心安である。Regarding aldehydes, formalin, paraform, hexamine, acetaldehyde, etc. are used.Water is safe because the phenolic 4111 fat and alkali metal hydroxide are uniformly coated on the refractory particles. be.
又、多丁き゛ると熱風による硬化が遅くなる。フェノー
ル性樹脂100止童部に対して5〜500里鼠部、好1
しくに50〜200厘童部用いらn/S。Also, if the number of sheets is too large, curing by hot air will be delayed. Phenolic resin: 5 to 500 feet per 100 feet, good 1
In particular, 50 to 200 children use n/S.
アルカリ金属の水酸化物に、フェノール性水酸基と親水
性の基音つくり水酸基の極性音強め、耐火物粒子と(/
J接眉力會人きくし更にフェノール性樹脂とエポキシ樹
脂との反応の触媒として働くものと考えらILる。たと
えは水酸化ナトリウム、水酸化カリウム、水酸化リチウ
ムCt、J1m1kに混81勿が用いらfL、親水性の
程度から水酸化ナトリウムが好ブしい。アルカリ金納の
水酸化物C/J配付狽は、フェノール性樹脂100皇翔
Sに対して1〜100連魅都好1しくに10〜6011
垣都用いら1[る。多丁さ゛ゐと熱j虱による硬化が遅
くなり少な丁き゛ゐとエポキシ樹脂との反応速度も遅<
z リ鋳型強度も小さくなる。Alkali metal hydroxide, phenolic hydroxyl group, hydrophilic fundamental sound creation, polar sound reinforcement of hydroxyl group, refractory particles and (/
It is also thought that the phenolic resin acts as a catalyst for the reaction between the phenolic resin and the epoxy resin. For example, sodium hydroxide, potassium hydroxide, lithium hydroxide Ct, and J1m1k may be mixed with fL, but sodium hydroxide is preferable from the degree of hydrophilicity. The distribution of hydroxide C/J in alkali metal is 1 to 100 times per phenolic resin 100 to 10 to 6011 times.
Kakito user 1 [ru. If there is a large amount of wood, the curing due to heat lice will be slowed down, and the reaction rate between the epoxy resin and the epoxy resin will also be slow.
z The mold strength also decreases.
エポキシ!射)3kllD、7 cノール性水酸基とエ
ポキシ基が反応し分子量が人きくなり疎水性が大となり
鋳型強度を向上させるものであめ。a)フェノール性樹
脂とb)水とC)アルカリ金h4(/、)水酸化物とd
)心安に応じてアルコール類からlる粘結材料は熱風[
Lll)硬化し鋳型用粘結材料として使用できるが、多
湿##fには水ガラス−炭酸ガス鋳型と同じ工9にv:
1型り強度が低下する欠点がある。C(L)欠点を改岩
丁々πめVこエポキシ樹脂ケ人rIるOとにニリンエノ
ール性水敵基とエポキシ基か反応し1分子量が人きくな
り疎水性が大となり多湿時の鋳型強度の低下を防ぐもの
と考えらILゐ0
ここでいうエポキシ樹脂と1町−股に分子内&lLエポ
キシ基會含む化名物であり肌常エホキシ樹脂と称さrL
/bものすべて上官み、エボキ7当童及びグリシジルエ
ーテル型、クリシジルエステル型、脂環型骨り樹脂構誼
に制限烙ILない。又樹JJiiC/、I形状にも制限
さ′i′Lない。一般には耐火物粒子に附子ゐ被板効果
ヶ人さく丁ゐたの低粘性のものが好1しく、史に好1し
くに低分子化合物でエポキシ当MUJ小式なものがよい
。Epoxy! 3kllD, 7cNol hydroxyl group and epoxy group react to increase molecular weight, increase hydrophobicity, and improve mold strength. a) Phenolic resin b) Water C) Alkali gold h4(/,) hydroxide and d
) Depending on your safety, the caking material from alcohol can be hot air [
Lll) It can be hardened and used as a caking material for molds, but for high humidity, use the same process as water glass-carbon dioxide molds.
One drawback is that the strength of the mold is reduced. C (L) The defect is corrected by the rock, and the epoxy resin reacts with the niline enol water group and the epoxy group, and the 1 molecular weight increases, and the hydrophobicity becomes large, and the mold strength in high humidity increases. It is thought that it prevents the deterioration of IL20.The epoxy resin referred to here is a chemical product that contains an epoxy group in the molecule and is commonly referred to as epoxy resin.
/b are all superior, and there are no restrictions on the structure of the EBOKI 7 and the glycidyl ether type, cricidyl ester type, and alicyclic type resin structure. It is also not limited to the tree JJiiC/, I shape. In general, it is preferable to use a low viscosity material that has a refractory coating effect, and a low-molecular-weight compound such as epoxy or MUJ type is generally preferable.
又υ1粘性あるいにtied型りもりに醪剤會ざ5加し
゛てもよい。この溶媒についてはエポキシ化合物全浴
解するものであILは例でも良く、通常rJアセトン、
メチルエテルケトン、シクロヘキサノン等θケトン知、
トルエン、シクロヘキサノンナフサ旬・が使用さILる
〇
又ム桁1エエボキシ樹脂も使用できる。You may also add 5 parts of a mulch to 1 part of the viscosity or tied consistency. This solvent is one that completely dissolves the epoxy compound, and IL may be used as an example, and is usually rJ acetone,
Theta ketones such as methyl ether ketone and cyclohexanone,
Toluene and cyclohexanone naphtha are used, but epoxy resin can also be used.
エポキシ樹脂の配付にはフェノール性樹脂100虚菫部
に、対してQ、7〜200及亀瀬が好ましい。多丁さ々
と熱ノ虱による硬化速度が遅くなり、少々すさると効果
がない。For distributing the epoxy resin, it is preferable to use a phenolic resin of 100 violet parts and Q, 7 to 200 parts and Kamise. The curing speed slows down due to excessive heating and heat lice, and if it cools down a little, it becomes ineffective.
本発明の枯帖相科VこiJ必要に応じてアルコール類を
配付することがで@る。Alcohol can be distributed as needed to the present invention.
アルコール類としては低級−1曲アルコールと多価アル
コールが使用できる。As alcohols, lower-1 alcohols and polyhydric alcohols can be used.
低級−価アルコールな、フェノール性衝脂り耐火物粒子
へQ−)波覆性を良くシ、更に熱J虱による粘結材料C
lJ堀粘會促進し、粘結カを向上さゼる効果がある。又
多価アルコールは釣型強役を高め鋳型の肌を艮〈する効
果がある。アルコール類とじては、メタノール、エタノ
ール、 n −グロビルアルコール、イン7゛ロビル
アルコール、t−ブチルアルコール、エチレングリコー
ル、グロビレングリコール、グリセリン、ジエチレンp
’ +) コール、ジグロビレンクリコール、トリメテ
ロールグロバン、トリメチロールエタン、ソルビット、
マンニット、ズル7ツド等り一槙又VJ重付物が用いら
nlそ(/J使用tiL&ユフェノール住樹脂400及
倉部に対しで60Q電i部以下が好ましい。多丁き゛る
と熱風vL L /b硬化か悲くなる欠点がある。Lower-hydric alcohol, phenolic fat refractory particles Q-) Good wave-breaking properties, and also caking material C by heat
It has the effect of promoting lJhori adhesion and improving caking force. Polyhydric alcohol also has the effect of enhancing the strength of the fishing mold and giving the skin of the mold a distinct appearance. Alcohols include methanol, ethanol, n-globyl alcohol, in7-globyl alcohol, t-butyl alcohol, ethylene glycol, globylene glycol, glycerin, diethylene p
'+) Cole, diglobylene glycol, trimetherolgloban, trimethylolethane, sorbitol,
When VJ-heavy materials such as Mannit, Zuru 7, etc. are used, it is preferable to use 60Q electric parts or less for 400 parts and 400 parts of tiL & euphenol resin used. b There is a drawback that it is hard and sad.
本発明に用いらnる耐火物粒子に鋳型り製逅に通常用い
ら1するもりlら使用−〇きる。たとえはシリカ砂、ジ
ルコン砂、オリピン砂、クロマイト砂等か用いらfL/
b0
又グラファイト粉、コールダスト等(’J li5’;
i力19勿t@型用組成物VC象加することも可能であ
4〕。The refractory particles used in the present invention are prepared using a mortar normally used in mold making. Examples include silica sand, zircon sand, oripin sand, chromite sand, etc. fL/
b0 Also graphite powder, cold dust, etc. ('J li5';
Of course, it is also possible to add VC to the @-type composition 4].
粘結材料の耐火物粒子への重付方法に裏付に規足するも
のではないが、ン昆@磯とじてはスピードミキサー、連
続ミキサー、マー2lど連線性υあるものが好ましい。Although there are no particular restrictions on the method of applying weight to the refractory particles with the caking material, it is preferable to use a speed mixer, a continuous mixer, a mer 2l, etc. that have continuity υ.
本発明ICJ:6粘結材料ケ耐火物粒子に硲カロ混練し
/ζ胸型用ホ1【成吻a蜜閉谷器に保イチするCとが好
ましいが、好1しくはン昆@俊l/8べく迷や力・に使
用する〇
熱風の温度vCついては50℃〜200 ’CQもので
艮く粘結材料中の水分を除去できT’Lは良い。ICJ of the present invention: 6 Caking material is kneaded with refractory particles / ζ Breast-shaped ho 1 [C which is kept in a proboscis occlusion device is preferable, but preferred is Nkon @ Shun 〇The temperature of the hot air VC used is 50°C to 200'CQ, which can remove moisture from the caking material and has a good T'L.
又佃)」iその他を配付した銅火物粒子會型込めした除
にその粒子間ケ辿過1−るのVこ必要l圧力、流迷紫も
っん熱風でめfLばよい。In addition to the copper refractory particles distributed in the mold, the pressure required to trace between the particles is sufficient with hot air.
熱風の宿は鋳型か硬化し木型等のパターンから抜型でき
る強度に達する葦で吹き込めは良い。It is best to blow hot air into molds or reeds that have hardened and are strong enough to be cut out from patterns such as wooden molds.
通常な圧力to 0.1〜5.0 kg/cmで0.5
〜5分あIL秩良く、鋳型の大きさ、耐火物粒子の通気
性によって異ってくる。0.5 at normal pressure to 0.1-5.0 kg/cm
It takes about 5 minutes, depending on the size of the mold and the air permeability of the refractory particles.
本発明VこLる粘結材料に耐火物粒子にざ≦加重付して
り1型用M成物として使用さILる。耐火物粒子へ(/
J姉加混宙は均一に混合さfしていることが好1しく、
耐火物粒子に均等に被覆さnていることが史に好ブしい
。粘結材料の使用量に耐火物粒子100df童部に対し
て好’El、<Uo、5〜20車市部さらに好1しくに
1〜10M量部用いらIIる。耐火物粒子への冷力1方
法は特に規定するものでにないが、粘結相■の各成分の
一部または全部tめらかじめ重付丁ゐことも、水、アル
コール類に浴かして浴液状、乳化状、懸濁状として添加
し粘結材料とすることができゐ〇好1しくけあらかじめ
フェノール性制御iEのアルカリ金属水浴液と必殺に応
じてアルコール類の8!58物の混合浴液をつくってお
き、耐火物粒子に(−11,とエポキシ樹脂ケ重付しで
鋳型用組成物とする。The caking material of the present invention is loaded with refractory particles and used as a type 1 M composition. To refractory particles (/
It is preferable that the J sister mixture is uniformly mixed,
It is preferable that the refractory particles be coated evenly. The amount of caking material used is preferably 5 to 20 parts, more preferably 1 to 10 M parts per 100 df of refractory particles. Cooling force on refractory particles 1 The method is not particularly prescribed, but some or all of the components of the viscous phase may be cooled to a smooth, damp, heavy layer, or immersed in water or alcohol. It can be added as a bath liquid, emulsion, or suspension to form a caking material. A mixed bath liquid is prepared, and a molding composition is prepared by adding an epoxy resin to the refractory particles (-11).
以下本発明CtJ実施例を示す。Examples of CtJ of the present invention are shown below.
実施例1
フェノール性柚j脂(a)clJ製造法冷却器、(“ジ
拌装匝全備えIC四つロフラスコVこフェノール940
g、37%ホルムアルデヒド240g、80%パラホル
ムアルテヒド190g、及びIN塩酸4gを入fL還流
幅度(102°C)T:2 hr及尾、させた後脱水濃
縮し軟化点85°Cす(ノボラック型)フェノール樹脂
(a)を得lこ O
v、J型用粘tier11配付砂の製造法遠州鉄工製ス
ピードミキサー(5kg容量)才用い石見6号珪砂4k
gケ入11、上記で侍たフェノール性II脂(a) 6
0 gと水60gと水酸化ナトリウム+Ogとメタノー
ル30gよりなるイ■脂俗故とエビコー)828(油化
シェルエポキシ社製、エポキシ当布184〜194、分
子量約580、ビスフェノールA型、エポキシ[1刀W
、)20gを冷加し2分間重付し粘鮎拐料配付砂會侍た
。Example 1 Phenolic citron fat (a) clJ production method Cooler (Four IC four-roof flask with full stirring capacity V-phenol 940
g, 240 g of 37% formaldehyde, 190 g of 80% paraformaldehyde, and 4 g of IN hydrochloric acid. Type) Obtain phenolic resin (a) Ov, method for producing viscous tier 11 distributed sand for J type Speed mixer made by Enshu Tekko (5 kg capacity) 4k Iwami No. 6 silica sand
g 11, Phenolic II fat (a) mentioned above 6
0 g, water 60 g, sodium hydroxide + Og, and methanol 30 g. Katana W
, ) 20g was cooled and weighed for 2 minutes, and served at a sand party where the sweetfish was distributed.
圧縮強度側ボ用試験片(/−J製造法
侍ら11−1ζ粘粕拐料配6砂155gを50φυ木型
に人II−ランマーτ用いてつさ固め50φ×50mm
高さり試1灰片會成型し120℃(IJ熱1戦を3、
[J kg / cm” (/J正圧力5分間通気し圧
縮強度試駁片倉僧た。C(/J試馳片會用いて抜型1分
体り圧縮強度25℃、65%RH(/J雰囲気中に24
hr放置抜の圧縮強度お工ひ抜型俊丁ぐに25°C1
水張りデシケータ中に24hr放随佐の圧動強度を測ボ
し’fc。Test piece for compressive strength side (/-J manufacturing method Samurai et al. 11-1 ζ lees filtered 6 sand 155 g was made into a 50φυ wooden mold using a human II-rammer τ to make a 50φ×50mm
Height test 1 ash piece molding at 120℃ (IJ heat 1 match 3,
[J kg/cm" (/J Positive pressure for 5 minutes to test the compressive strength. 24 inside
Compressive strength after leaving for hr 25°C1
The pressure force was measured for 24 hours in a desiccator filled with water.
衣−1に試験片の測定値?示しπ0
実施例2
フェノール樹B盲に実施例1で倚らrl、た樹脂(a)
を用いに0粘結相科配付砂に珪砂(石見6号)4kgに
対してよ8ピで侍らn次フェノール性樹脂(a) 60
gと水80gと水酸化ナトリウム3[]gとクリセリ
ン20gよりなる小H月行m液とエヒ゛コ−)+001
(?li化シエルエホギシ社製一点68°C1エポキシ
当倉450〜500、分子量約900のエポキシ樹脂)
40g′(!−アセトン20gに溶解芒せた鶴1刀旨浴
欣ケ硝力11し2分1u4混甘しイ4すた。実施?!I
+と同じ方法で試験片を作成し測足ホ占朱全表−IV
C−w、L、友0
比較1タリ
フエノール性桓(脂に夾万出秒jl lで倚らIした1
劇刀百會用いた。枯粕拐科配台砂は芙施鉋11と同じ方
法でエヒ゛コート828會尚a口しないで製造しπ0実
施例1と同じ方法で試験片を作JJy、L、測定帖来ケ
表−1に示し7?:。Measurement value of test piece on cloth-1? Indication π0 Example 2 Phenolic resin B blinded in Example 1, resin (a)
Using 4 kg of silica sand (Iwami No. 6), distribute n-order phenolic resin (a) 60 to 4 kg of silica sand (Iwami No. 6) using 8 pi.
g, 80 g of water, 3 g of sodium hydroxide, and 20 g of chrycerin.
(One point 68°C 1 epoxy resin made by Ili Chemical Co., Ltd. 450-500, molecular weight approximately 900)
40g' (! - Dissolved in 20g of acetone 1 Tsuru 1 sword salt bath 11 pieces of water and 2 minutes 1 u 4 mixed with 4 pieces. Implementation?! I
A test piece was prepared in the same manner as + and the test piece was measured.
C-w, L, friend 0 Comparison 1 Tarifenolic acid (added to fat) 1
I used Gekito Hyakukai. The dried lees-carrying sand was manufactured in the same manner as Fusei Plane 11 without applying an air coat. Show 7? :.
表−1測定精米 注1)直後941度に抜ηj後凰分放散して側翼した。Table-1 Measured milled rice Note 1) Immediately after, at 941 degrees, the aircraft ejected ηj and dispersed its tail and flew to the side.
注21 (B)/囚は多歯時の鋳型強ルニ低下の6テ
価方法とした。Note 21 (B)/Concept is a 6-value method for reducing mold strength when there are many teeth.
又実施?IJ+、2及び比較Vすで用いた粘縮材料配付
砂で中子ケつくり鋳鉄を納込み砂洛ち性r峻祭したとこ
ろいずスLも良好な鋳型の崩♂性會もっていることを確
認し?c。Implemented again? IJ+, 2 and Comparison V When we delivered the core-making cast iron using the cohesive material distribution sand used previously and tested it for sand lubricity, we found that Izusu L also had good mold crumbling properties. Confirmed? c.
Claims (1)
リ金属の水酸化物とd)エホキシ位1脂とe)必要1f
C応じてアルコール類からなる熱風硬化性鋳型粘結材料
。 2、 アルカリ金属υ水酸化!IJか水酸化ナトl)ラ
ムでめるt1守罰#jI求の孕r力j身↓1歩m1戦の
熱ノ虱イ辺2化性釣型粘鮎拐料。1.8) Phenolic ff1f fat, b) water, C) alkali metal hydroxide, d) epoxy position 1 fat, and e) necessary 1f.
A hot air-curable mold caking material made of alcohol according to C. 2. Alkali metal υ hydroxide! IJ or sodium hydroxide l) Ram t1 defense punishment #jI request's impregnating power j body ↓ 1 step m1 match's heat lice, side 2 conversion fishing type sticky sweetfish killing fee.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17052482A JPS5961546A (en) | 1982-09-29 | 1982-09-29 | Binder material for casting mold curable by hot wind |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17052482A JPS5961546A (en) | 1982-09-29 | 1982-09-29 | Binder material for casting mold curable by hot wind |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS5961546A true JPS5961546A (en) | 1984-04-07 |
Family
ID=15906532
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17052482A Pending JPS5961546A (en) | 1982-09-29 | 1982-09-29 | Binder material for casting mold curable by hot wind |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5961546A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110280713A (en) * | 2019-08-02 | 2019-09-27 | 承德北雁新材料科技有限公司 | Bonding agent and its preparation method and application, resin-coated sand shell mould and preparation method thereof |
-
1982
- 1982-09-29 JP JP17052482A patent/JPS5961546A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110280713A (en) * | 2019-08-02 | 2019-09-27 | 承德北雁新材料科技有限公司 | Bonding agent and its preparation method and application, resin-coated sand shell mould and preparation method thereof |
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