JPS58202947A - Production of casting mold - Google Patents

Production of casting mold

Info

Publication number
JPS58202947A
JPS58202947A JP8677582A JP8677582A JPS58202947A JP S58202947 A JPS58202947 A JP S58202947A JP 8677582 A JP8677582 A JP 8677582A JP 8677582 A JP8677582 A JP 8677582A JP S58202947 A JPS58202947 A JP S58202947A
Authority
JP
Japan
Prior art keywords
mold
alcohol
hydroxide
water
refractory particles
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.)
Granted
Application number
JP8677582A
Other languages
Japanese (ja)
Other versions
JPS615817B2 (en
Inventor
Shigeo Sase
佐瀬 茂雄
Masae Kuroda
黒田 正栄
Yukio Yoshimura
幸雄 吉村
Susumu Koarai
古新居 進
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.)
Resonac Corp
Original Assignee
Hitachi Chemical 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 Hitachi Chemical Co Ltd filed Critical Hitachi Chemical Co Ltd
Priority to JP8677582A priority Critical patent/JPS58202947A/en
Publication of JPS58202947A publication Critical patent/JPS58202947A/en
Publication of JPS615817B2 publication Critical patent/JPS615817B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22CFOUNDRY MOULDING
    • B22C1/00Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
    • B22C1/16Compositions 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
    • B22C1/167Mixtures of inorganic and organic binding agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Inorganic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Molds, Cores, And Manufacturing Methods Thereof (AREA)
  • Mold Materials And Core Materials (AREA)

Abstract

PURPOSE:To accelerate curing and to improve productivity by mulling a binding material consisting of an alcohol soluble phenolic resin, hydroxide or oxide of polyvalent metals, water, and hydroxide of alkali metals and refractory particles, putting the mixture into a pattern, permeating compressed air therethrough and permeating CO2 through the casting mold after cooling then removing the mold. CONSTITUTION:A binding material for a casting mold to be cured by gaseous CO2 consisting of an alcohol soluble phenolic resin, hydroxide or oxide of polyvalent metals, or both, water, hydroxide of alkali metals and, if necessary, polyhydric alcohol and lower monohydric alcohol is prepd. The binding material and refractory particles are mulled to produce system sand which is then molded. Compressed air is permeated through the obtained sand mold to cool the same, whereafter CO2 is permeated through the mold to cure the same and the mold is removed.

Description

【発明の詳細な説明】 本発明に炭酸ガスr(工V硬化さゼる#型CtJ製造方
f&に関するものである。 a)アルコール溶性フェノ
ール性樹脂とb)多価金属の水酸化物お1ひ/またにそ
Q)M化物とC)水とのアルカリ金属の水酸化物とC)
必資に応じてQkIIlbアルコールとf)必資に応じ
て低級111111アルコールからなる粘顧材料と耐火
物粒子を混螺したtのに炭酸ガスを通気する仁とvtt
v&化させ#1型を製造する方法かあるか、時に夏場に
鋳型強度か低下するという欠点かあり、大qms型や複
雑な鋳型の製造か困難であ−)た0本発明a轡朧強度の
低下上防止する鋳型の製造方法V(関するものであるQ
本@曲に迅速Ka造でき王に夏場に%鋳at強度(tJ
低下t#なわない鋳銅り喪慮方法を提供するもりでめる
◇ 次々tJJl場と両型強度の低下する原因會鋭意慣肘し
fc和未以下υことがわかり本発明rt至った。耐アル
コール溶性フェノール性樹脂とb)多価金^O水酸化物
2Lび/1だにその欧化物とC)水とのアルカリ金mυ
水酸化物とe)必Ji!に応じて多価アルコールとf)
必資に応じて低級−価アルコールからなるM型枯軸材料
と耐火智粒子VC混練した%ctJに炭皺ガス會周気す
ると鋳型粘 ゝ・軸材料(IJ酸成分あるアルコール浴
性フェノール性@脂多勧金属及びアルカリ雀属か炭酸ガ
スυ剋気に19アルコール−性フェノール性(I[l庸
の多価金属塩と炭酸アルカリを生叙す/)礪せr(中和
熱か生じ鋳型の渦紋が上昇する。炭酸ガス通気による#
I8型の編匿差に鋳型の大きさ、鋳型粘結材料の配付1
tあるい0戻酸ガス@VtLって異なり通常0〜40℃
ぐらいでめゐ。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing #-type CtJ that cures carbon dioxide. Q) M compound and C) alkali metal hydroxide with water and C)
QkIIlb alcohol depending on the required amount and f) a mixture of adhesive material made of lower 111111 alcohol and refractory particles depending on the required amount, and a vtt for aerating carbon dioxide gas.
Is there a way to manufacture the #1 mold by converting it into v&?It has the drawback that the mold strength sometimes decreases in the summer, and it is difficult to manufacture large qms molds or complicated molds. Mold manufacturing method V (related to Q
% casting strength (tJ
◇ The cause of the decrease in tJJl field and the strength of both molds has been studied and it has been found that the fc sum is less than υ, which led to the present invention. Alkali gold mυ of alcohol-resistant phenolic resin, b) polyvalent gold^O hydroxide 2L/1 and its European compound, and C) water.
Hydroxide and e) Necessary Ji! f) with polyhydric alcohol depending on
Depending on the requirements, M-type dead shaft material consisting of lower-hydric alcohol and refractory particles VC kneaded with %ctJ are exposed to a charcoal gas atmosphere to create mold viscosity. 19 Alcohol-based phenolic (I [l] produces polyvalent metal salts and alkali carbonates in the presence of carbon dioxide gas or alkali metal salts). The vortex rises. # due to carbon dioxide aeration
I8 type compaction difference, mold size, distribution of mold caking material 1
t or 0 return acid gas @VtL is different, usually 0 to 40℃
That's about it.

物に夏場(lJよりに気硯り簡い揚台にtJ、炭酸ガス
通気前で鋳型温度に40℃ぐらいとなりj!VL戻酸ガ
スによる発熱でM型の−kが40〜80℃VLなること
%1ある。こりよりな礪せにt1絢型υ枯粕材++が熱
に工V蒸さn九状態となるため枯粕材料の主成分である
アルコール耐性フェノール性w脂が軟化現象奮起こし鋳
型強度低下の原因でtbることかわかっ1ζ0 して冷却し、その後炭酸ガスを通気して脱脂丁ゐことV
t工9炭酸ガス3+!!1.、一時の反応熱VL Lる
アルコール溶性フェノール性樹脂υ軟化を防止し鋳型の
癩度會向土させ、迅速VC鋳型を製造できるようにした
もυであるoIE紬9気を通気するυは気化熱t−奪い
組型内部1でM効に冷却できるからである。
Especially in the summer (tJ is easier to take care of than IJ), the mold temperature is about 40℃ before carbon dioxide gas ventilation, and the -k of M type becomes 40~80℃VL due to the heat generated by the returning acid gas. This is %1.Due to stiffness, the T1-type dried lees material becomes steamed due to heat, which causes the alcohol-resistant phenolic fat, which is the main component of the dried lees material, to soften. It was found that tb was the cause of the decrease in mold strength.The mold was heated to 1ζ0, cooled, and then degreased by passing carbon dioxide gas through it.
T-work 9 carbon dioxide gas 3+! ! 1. , the alcohol-soluble phenolic resin υ prevents the temporary reaction heat VL L from softening, reduces the leukemia of the mold, and enables rapid production of VC molds. This is because the heat t-scavenging type interior 1 can provide M-effect cooling.

1丸空′Aを通気するとfs型の通気性がよくなり、後
から通すCO−か鋳型の全体にしくゆきわたる様になり
CO鱈O節約VL %なる。
By ventilating 1 round 'A', the air permeability of the fs mold will be improved, and the CO passed through later will be properly distributed throughout the mold, resulting in CO cod O saving VL%.

又鋳型O崗度に強制冷却にLり40℃以下、更に050
℃以下と低いはと好ましく、かつ短時間rcg却する方
か好ましい。低くするはど両型の強直低下を抑えるCと
ができる。
In addition, the mold temperature is forced to cool to 40℃ or less, and further to 050℃.
It is preferable that the temperature is as low as ℃ or less, and it is preferable that the rcg temperature be cooled for a short time. By lowering the C, it is possible to suppress the decline in both types of tonicity.

又圧縮空気(tJI!!度に低い方が好ましく又圧力1
j藺い方が好ましい0史PC木型等のパターンにベント
η(−ルを取りつけガスの21!I気を工くする方が良
い。
Also, compressed air (tJI!! It is preferable that the pressure is lower than 1 degree)
It is better to attach a vent η (-) to a pattern such as a 0-history PC wooden mold, which is preferable to be smooth, and to take care of the gas.

不発明でいうアルコール溶性フェノール性樹脂とげ1ン
工ノール性樹脂七重貢で10倍賃の水と25′Cで十分
yc攪拌した礪せでも、肉眼で判別−〇きるPCごり音
生ずる工うな非水溶性の樹::、・・1≧、。
Even if the alcohol-soluble phenolic resin thorn 1 and the alcohol-soluble resin 7-layer compound is sufficiently stirred at 25'C with 10 times the amount of water, it can be determined with the naked eye. Water-insoluble tree::,...1≧,.

脂をいう。丁なわ 水混和度が10以下の樹脂tいう0
そして樹脂中に両部水溶性樹脂を言んでいICとして%
使用さILる樹脂全体として上述の性質?:有していn
ばよい。
Refers to fat. Ding rope Resin with water miscibility of 10 or less
And both parts of the resin are water-soluble resins and are expressed as IC%.
Does the IL resin used have the above-mentioned properties as a whole? : have n
Bye.

本発明で用いらnるアルコール溶性フェノール性樹脂と
してaいわゆるアルコール溶性フェノールホルムアルデ
ヒド系樹脂だけでなくフェノール変性キシレン樹脂、フ
ェノール変性トルエン樹脂、カシェ−樹脂、DFK(j
ll抽油6M脂などそL)^分子骨格υ中に多価金輌と
塩を形成するフェノール性水酸基t%っているW脂であ
nに=い。
The alcohol-soluble phenolic resins used in the present invention include not only so-called alcohol-soluble phenol formaldehyde resins, but also phenol-modified xylene resins, phenol-modified toluene resins, cachet resins, and DFK (j
It is a W fat that has t% of phenolic hydroxyl groups that form salts with polyvalent metals in its molecular skeleton υ.

丸とえFiミツエノールホルムアルデヒド41 Jim
 Kついてい見は、−収Vt水醪性2エノールホルムア
ルデヒド4U旨とアルコール溶性ンエノールホルムアル
デヒド樹脂とに大別さnる0水溶性2工ノールホルムア
ルデヒド4M傘にフェノールとホルマリンtアルカリ触
媒下でMA1!r反応をおこない′m甘せか水漏性を失
う以前に冷却にLり反応を停止場ぜ7t%ので、七の1
1曾物に28ノ一ル三核体以下を主成分とする平均分子
量か200程度の低分子υ@hぽである・こnに対して
アルコール溶性フェノールホルムアルデヒド側鹿0s6
分子の樹脂である◎水浴性の2エノール性樹側0樹脂の
分子1/kが小さく粘性も低いため型込めして炭酸ガス
を吹き込んだ揚台のIM友か低く。
Marutoe Fi Mitsuenol Formaldehyde 41 Jim
Regarding K, it can be roughly divided into - yield Vt water soluble 2 enol formaldehyde 4U and alcohol soluble enol formaldehyde resin 0 water soluble 2 enol formaldehyde 4M umbrella phenol and formalin t MA1 under alkaline catalyst ! If the reaction is carried out, the reaction must be stopped by cooling before it loses its water leakage property.
1. It is a low molecular weight υ@hpo with an average molecular weight of about 200, which is mainly composed of 28 nor trinuclear bodies.For this, the alcohol-soluble phenol formaldehyde side is 0s6.
Molecule resin ◎Water bath property 2 enol tree side 0 The molecule 1/k of the resin is small and the viscosity is low, so it is an IM friend of the lifting platform where carbon dioxide gas is blown into the mold.

且つ放置俊IZJ強直も低い・従って本発明で用いらn
るフェノール性樹脂にその多価金属塩か水に111階で
、〃為つ十分な粘幀力に%たぜるため、分子′IILo
篇いもqJか工く、数平均分子量が好筐しくoaoo以
上、さらに好1しくに500以上、さらに好ましくα8
00以上υものかLい。
In addition, the IZJ tonicity of neglected children is also low.Therefore, they are not used in the present invention.
In order to give the phenolic resin its polyvalent metal salt or water 111% to give it sufficient viscosity, the molecule 'IILo
The number average molecular weight is preferably oaoo or more, more preferably 500 or more, and even more preferably α8.
00 or more υ or L.

4莞明rL用いられるアルコール心性フェノール社倒繍
にレゾール型3ノボ2ツク麿、Nメチレンレゾール、ジ
メチレンエーテル誠レゾール。
4 Guanming rL is used for resol type 3 novo 2 tsukumaro, N methylene resol, dimethylene ether resol for the alcohol-based phenol company embroidery.

ホルマール盟しゾール等#脂のMせ形式vc関係なくア
ルコール層性2エノール注IM脂であnば本目的yt1
j!!用することかで1!%樹脂曾或原料で6るフェノ
ールailKついて%2エノールだけでなくクレゾール
、ブチル2エノール、ビス2エノール、ノニルフェノー
ル、カテコール、レゾルシノールなど使用することがで
きる・アルデヒド類についてもホルマリン、パ2ホルA
、へキT<ン、アセトアルデヒドなどの低級アルデヒド
tW用したフェノール系樹脂が使用で@ 4 。
Formal and sol, etc. # Fat M type VC Regardless of alcohol layer 2 enol injection IM fat, this purpose yt1
j! ! 1 because you can use it! Regarding the 6% resin and raw materials, not only 2enol but also cresol, butyl2enol, bis2enol, nonylphenol, catechol, resorcinol, etc. can be used.For aldehydes, formalin, pa2forA, etc. can be used.
, hexane, phenolic resins containing lower aldehydes such as acetaldehyde are used.

多価金属の水酸化物お工ひ/筐fc0その酸化物として
* Cae Mgl At、 Zn、 13a、 Fe
、 Ni、 Ti。
Hydroxide production of polyvalent metals/Casing fc0 As its oxide * Cae Mgl At, Zn, 13a, Fe
, Ni, Ti.

Si、Sn などの水酸化物5M化吻が使用で!!るか
、フェノール性樹脂との反応性、水との親和性から好筐
しくにアルカリ生金j14v水酸化智おLび/またに濠
化物が用いらn%特にCm、 Ba。
5M hydroxides such as Si and Sn can be used! ! However, alkaline raw metals are preferably used due to their reactivity with phenolic resins and affinity with water, especially Cm and Ba.

造(Li水量化物2工び/1九にそυ酸化管か好ましい
。Ca以外Vアルカリ土金属の水酸化物。
Preferably, a Li hydroxide (Li hydrated 2/19 oxidation tube) is used. Hydroxides of V alkaline earth metals other than Ca.

酸化物に水酸化カルシウム、酸化カルシウムと併用する
ことlc L 9効果的に用いらnるO配合itにアル
コ−に冶注フェノール社廟脂100重it s tit
対して好’! t、<010〜5001its、用いら
3る0 水にアルコール層性′2エノール性樹脂100重量奄に
対して好ましくに5゛0〜5001童部用いらrする0 アルカリ金属としてに水酸化ナトリウム、水壷化カリウ
ム、水酸化リチウムか用いらas !1水性の8度から
水酸化ナトリウムが針筒しいOアルカリ金属の便用ii
 rJ 7 s)−ル性@珈10Omjli部に対して
好ましくに10〜100ム倉都用いらjL 4 。
Calcium hydroxide and calcium oxide can be used in conjunction with LC L 9. It can be effectively used in combination with alcohol.
I like it! t, <010~5001its, using 30% alcohol layer in water and preferably using 500~5001% per 100 weight units of enolic resin0 as alkali metal, sodium hydroxide, Potassium water, lithium hydroxide, etc. are used as! 1 Aqueous 8 degrees to sodium hydroxide is acrylic O alkaline metal toilet ii
rJ 7 s) - preferably 10 to 100 μL 4 to 10 Omjli portion.

多価アルコールとしてエチレングリコール。Ethylene glycol as a polyhydric alcohol.

プロピレングリコール、グリセリン、ジエチレングリコ
ール、ジプロピレンクリコール、トリメチロールプロパ
ン、トリメチロールエタン。
Propylene glycol, glycerin, diethylene glycol, dipropylene glycol, trimethylolpropane, trimethylolethane.

ソルビット、マ′ンニット、ズルシット等が単独又tユ
山付して用いらnる0 ◆画アルコールと共に必要に応じて低級1価アルコール
を併用することも用層である・低級1価アルコールとし
てメタノール、エタノール。
Sorbit, mannit, zurcit, etc. can be used alone or in combination. ◆It is also possible to use lower monohydric alcohol in combination with painting alcohol if necessary. ・Methanol is used as a lower monohydric alcohol. ,ethanol.

nプロピルアルコール、イソ10ビルアルコール、tブ
チルアルコール等が用いらn40多愉アルコール、低級
11iii+アルコールの使用態にそCぞ几アルコー1
.ル浴性フェノール性樹脂1003に電郁に対して好ま
しくに1〜100真        1゜iii郁用い
らnる0 本発明rc用いらr′Ldb耐火豐粒子にMffiU顧
造yt遡常用いら几るtQJなら使用できゐO几とえば
シリカ砂、ジルコン砂、オリピン砂、クロマイト砂等が
用いらnる0 又グラファイト粉、コールダス)sum加物1に両型用
組成一に硲〃口TるCと% bJ馳で660粘細材料の
耐火物粒子への混付力法a特r(規足丁4%すで口ない
が、搗曾憤としてはスピードミキサー、連杭ミキサー、
マー2など連線性Oめるものが好I L、い、。
N-propyl alcohol, iso-10 alcohol, t-butyl alcohol, etc. are used.
.. Preferably, 1 to 100% of electric current is applied to the bath-based phenolic resin 1003. For example, silica sand, zircon sand, oripin sand, chromite sand, etc. can be used. % bJ 660 viscous material mixed into refractory particles a special method (required 4%) Although it is too much to say, as a speed mixer, a continuous pile mixer,
I like things that have continuity, such as Mar 2.

本発明rcよる粘組材朴を耐火物粒子l(6訓混練し7
t#I!&型用組成物σ密閉谷器に株存することが好ま
しいが、Ikf筐しくα混省佐なるべく速やかV(使用
する0 硬化に使用する炭絃ガスについてに必ずしも100%C
Omである必要になく炭酸ガスを富む気体であnI/i
工く、樹脂その他を配合した耐火物粒子を型込めした際
にその粒子間を通遍丁クリr(必要な圧力、流速t−4
つた炭酸ガスでめytは工い〇 炭酸ガスの菫に気菌が20℃以下のMe rc繭誠が硬
化し木型等のパターンから抜型できるtr吹き込めば艮
い0通常なガス圧081〜iokg/(1”t’3〜1
20秒h rt u良く、鉤mu大きさ。
Refractory particles l (kneaded 6 times and 7 times
t#I! It is preferable that the mold composition σ be present in a closed valley vessel, but the Ikf case and α should be mixed as quickly as possible.
It is not necessary that Om is a gas rich in carbon dioxide, but nI/i
When the refractory particles mixed with resin and other ingredients are placed in a mold, the particles are passed through the hole (necessary pressure, flow rate t-4
It is possible to make it with carbon dioxide gas 〇The air bacteria in the violet of carbon dioxide gas is hardened and can be cut out from patterns such as wooden molds.Normally gas pressure 081 ~ iokg /(1”t'3~1
20 seconds hrt u good, hook mu size.

耐火物粒子0通気性によって異つてくる◎′X発明vC
Lる枯紬材料に劇大物粒子に添加1甘して#勘用組II
L物として使用さrする・耐大物粒子へり踊加山付に均
一に混甘さnていゐことか好1しく、耐火物粒子rC均
勢に被覆さKしていることか史V(針筒しい。粘粕材料
υ使用輩a」火啼柁子toox’it部に対して好1し
くに0.5〜20飄IIL部ざらに好ましくに1〜10
ム菖部用いらiLる。耐火物粒子への添加方法に特に規
厘するものでにないが、粘帖材料QJ各成分υ一部また
に全部′Ikあらかじめ混合粉末とすることt1水、+
SS剤に浴力為して浴液状、乳化状、懸濁状として添加
し粘粕材料とすることができる◇好1しくにめらかじめ
アルコール溶性2エノール性樹脂のアルカリ金属水密液
と′4価アルコール又に多価アルコールと低級1価アル
コールり山付物の1曾溶液をつくっておき、耐火物粒子
にこnと多価金属の水酸化物νLび/箇たσ−tの酸化
物を混性して鋳型用組成物とする。
Refractory particles 0 Varies depending on breathability ◎'X invention vC
L Karatsumugi material is added to the large particles 1 and #kanyo group II
When used as a refractory material, it is preferable that the refractory particles have an evenly mixed sweetness on the edge of the refractory material, and that the refractory particles are evenly coated. The sticky material υ is preferably 0.5 to 20 for the toox'it part, and preferably 1 to 10 for the IIL part.
I use the irises. There are no particular restrictions on the method of addition to the refractory particles, but each component of the viscous material QJ may be partially or completely mixed into a powder in advance.t1 Water, +
It can be added to the SS agent in the form of a bath liquid, emulsion, or suspension to form a slime material.◇Preferably, an alkali metal watertight liquid of a smooth, moist, alcohol-soluble di-enol resin. Prepare a solution of tetrahydric alcohol or polyhydric alcohol and lower monohydric alcohol, and oxidize the hydroxides of polyvalent metals νL and σ−t on the refractory particles. The materials are mixed to form a molding composition.

こυL5に丁nは2エノール性樹脂に水浴液中で児全y
cアルカリ金属の親水性塩とな9.炭酸ガス通気俊、2
エノール性樹脂O多価金属塩の生成か容易となる〇 以下本発明會東施倒に1って灸に詐しく胱明するか、粘
細材料成分の種類および童に1うてに1本発明r[1p
Jら制限を受けない。
This υL5 is a mixture of two enolic resins in a water bath solution.
c Hydrophilic salts of alkali metals9. Carbon dioxide gas ventilation, 2
Enolic resin O facilitates the formation of polyvalent metal salts 〇 Below, the present invention will be applied to the present invention, and the moxibustion will be falsely revealed, depending on the type of viscous material component and one bottle per child. Invention r[1p
No restrictions apply to J et al.

以下実施?!It不丁◇ 冷却器1攪押装置kを備えた四ツ目フラスコにフェノー
ル940g、80%バラホルムアルテヒド280g&L
ひ’/sつ# 28 g t−人R4&jし還流龜度(
100〜105℃)で5時間加熱しyc盪脱水1111
4し、軟化点85℃υノボ2ツク型フェノール倒脂會得
た◎上記方法で侍らnycノボラック型フェノール樹:
・1M75gと水100gとNaOH10gとグリセリ
ン50gとメタノール15gjりなる樹脂溶液とCm(
OH)* 75 gt遠州鉄工製スピードξ中サすにて
6見6号し5kgと2分間混線し配合砂を得た。こり配
合砂1200grlOOφxtoommhの試IjIk
胸木型r(造型し圧#!!気にて冷却処理を行いその後
251 / m1n(iZ炭鈑ガス′に80秒通気した
・そ&J幀果會表−1に示した・我中−のa従来法であ
る。F’l&l■■に不発tp3yt本発明に希づくも
のである・ 六−11■釆 *圧m彊贋α炭酸ガス通気後60秒後に幽足した。
Will the following be implemented? ! It's incorrect ◇ In a four-eye flask equipped with a condenser and a stirrer k, 940 g of phenol and 280 g of 80% rose formaldehyde are added.
hi'/s #28 g t-person R4&j and reflux degree (
Heat at 100-105℃ for 5 hours and dehydrate by yc
4, a novolak type phenol resin with a softening point of 85℃υ was obtained. ◎The samurai nyc novolak type phenol resin was obtained by the above method:
・Cm (
OH) * 75 gt was mixed with 5 kg for 2 minutes using a No. 6 speed sander manufactured by Enshu Iron Works for 2 minutes to obtain mixed sand. Trial of stiff mixed sand 1200grlOOφxtoommhIjIk
Breast wood mold R (molded and cooled under pressure #!! air, then vented to 251/m1n (iZ coal board gas' for 80 seconds) a Conventional method.F'l&l■■Failure to erupt tp3ytThis is a method unique to the present invention.6-11■Bottle*Pressure m 彊falseαFailure to occur 60 seconds after carbon dioxide gas ventilation.

14〕 たエラに砂−型を冷却した後炭駿左ス七通気することに
エクiRJ澁時U鋳型強度の低下管改醤することかでき
7t。
14] After cooling the sand mold in the gills, the left side of the charcoal was vented to reduce the strength of the U mold.

Claims (1)

【特許請求の範囲】[Claims] 1、a)アルコール溶性フェノール性樹脂とb)多価金
属の水酸化物2工び/ま7trIその酸化物とC)水と
Φアルカリ金属の水酸化物とC)修景に応じて多価アル
コールとf)必要に応じて低級1fIJアルコールから
なる炭絨ガス硬化用鈎型粘粕材料と耐火物粒子とを混練
し沈配廿砂を造型して得らn沈砂型に圧締、空気を通気
して冷却し、そり後炭酸ガスを通気し脱型することを特
徴とするwaa!!の製造方法。
1. a) alcohol-soluble phenolic resin, b) polyvalent metal hydroxide, C) water and Φ alkali metal hydroxide, and C) polyvalent metal depending on the landscape. Alcohol and (f) charcoal gas made of lower 1f IJ alcohol if necessary.Knead the hook-shaped viscous material for hardening and refractory particles, mold the precipitated sand, press it into a precipitated mold, and blow air. Waa! is characterized by ventilation and cooling, and after warping, carbon dioxide gas is vented and demolded. ! manufacturing method.
JP8677582A 1982-05-21 1982-05-21 Production of casting mold Granted JPS58202947A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8677582A JPS58202947A (en) 1982-05-21 1982-05-21 Production of casting mold

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8677582A JPS58202947A (en) 1982-05-21 1982-05-21 Production of casting mold

Publications (2)

Publication Number Publication Date
JPS58202947A true JPS58202947A (en) 1983-11-26
JPS615817B2 JPS615817B2 (en) 1986-02-21

Family

ID=13896124

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8677582A Granted JPS58202947A (en) 1982-05-21 1982-05-21 Production of casting mold

Country Status (1)

Country Link
JP (1) JPS58202947A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017152589A1 (en) * 2016-03-08 2017-09-14 沈阳汇亚通铸造材料有限责任公司 Method for producing mould and core through curing sodium silicate sand for casting by blowing

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03113493U (en) * 1990-03-06 1991-11-20

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017152589A1 (en) * 2016-03-08 2017-09-14 沈阳汇亚通铸造材料有限责任公司 Method for producing mould and core through curing sodium silicate sand for casting by blowing

Also Published As

Publication number Publication date
JPS615817B2 (en) 1986-02-21

Similar Documents

Publication Publication Date Title
WO2010117022A1 (en) Curing agent composition
JP2011520615A (en) Methanesulfonic acid-containing catalyst in acid curing process
CN103059505B (en) CO2 cured alkaline phenolic resin and preparation method thereof
JPH02500753A (en) Modifier for aqueous base solution of phenolic resol resin
WO2012005213A1 (en) Manufacturing method of casting mold
JPS58202947A (en) Production of casting mold
JP6019046B2 (en) Organic binder for mold, foundry sand composition obtained using the same, and mold
JP2015123479A (en) Manufacturing method for self-curing mold, molding binder kit, and molding composition
US4113916A (en) Shell sand with improved thermal shock resistance
JP3453485B2 (en) Method for treating casting sand and method for producing mold
JPS6312700B2 (en)
CN114163210B (en) Self-hardening curing agent and preparation method thereof
CH659077A5 (en) TWO-COMPONENT COMPOSITION.
JP3250926B2 (en) Mold composition and method for producing mold
JPS5942581B2 (en) Self-hardening foundry sand composition
JP2018140438A (en) Binder composition for cast molding
JP7303680B2 (en) Binder composition for mold making
DE3639233A1 (en) COLD-HARDENING MOLD BINDING AGENT AND THE USE THEREOF
JPS6125451B2 (en)
JP2542144B2 (en) Binder composition for organic ester-curable foundry sand and method for producing mold using the same
JPS58202946A (en) Production of casting mold
JP3248825B2 (en) Mold production method
JP2020082185A (en) Additive for mold
JPH01166853A (en) Bond composition for mold
JP3250930B2 (en) Binder composition for mold, mold composition and method for producing mold