JPS6049830A - Production of casting mold - Google Patents

Production of casting mold

Info

Publication number
JPS6049830A
JPS6049830A JP15935283A JP15935283A JPS6049830A JP S6049830 A JPS6049830 A JP S6049830A JP 15935283 A JP15935283 A JP 15935283A JP 15935283 A JP15935283 A JP 15935283A JP S6049830 A JPS6049830 A JP S6049830A
Authority
JP
Japan
Prior art keywords
sand
mold
resin
resol
bisphenol
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
JP15935283A
Other languages
Japanese (ja)
Other versions
JPS6261375B2 (en
Inventor
Masae Kuroda
黒田 正栄
Takeshi Sumi
武志 澄
Yukio Yoshimura
幸雄 吉村
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 JP15935283A priority Critical patent/JPS6049830A/en
Publication of JPS6049830A publication Critical patent/JPS6049830A/en
Publication of JPS6261375B2 publication Critical patent/JPS6261375B2/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
    • B22C1/20Compositions 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
    • B22C1/22Compositions 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
    • B22C1/2233Compositions 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
    • B22C1/2273Polyurethanes; Polyisocyanates

Abstract

PURPOSE:To improve the collapsing property of a casting mold by heating the coated sand on which a compsn. contg. a block isocyanate compd. and a resol type phenolic resin is coated to cure said sand and to have the urethane bond resulting from the reaction of methyrol group and hydroxyl group, etc. generated by such curing. CONSTITUTION:The resulting product of addition reaction of a polyisocyanate compd. and an isocyanate block agent is used as a block isocyanate compd. A resol resin for which a bisphenol or the like is used for the purpose of maintaining the dry strength of the sand is used as a resol type phenolic resin. Said resin is obtd. by bringing 1.5-4.0mol formaldehyde into reaction with 1mol bisphenol A. The heating temp. in the stage of manufacturing the casting mold is 150-350 deg.C.

Description

【発明の詳細な説明】 本発明は鋳湯の製造方法に関丁るものでめり特に王にア
ルミニウム鋳物、合金鋳物など比較的鋳込温匿の低い鋳
物に用いられゐ鋳込÷俵の鋳型の崩壊性′!l:著しく
改良した鋳型の製造方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing casting metal, and is particularly applicable to castings with relatively low casting temperature, such as aluminum castings and alloy castings. Degradability of the mold! 1: This relates to a significantly improved method of manufacturing a mold.

従来から制量の製造方法にn狸々のプロセスがあるが甲
でもフェノール樹脂會用いにシェルモールド法は鋳型の
寸法安矩性に優れ、鋳型の肌もよ硬化速吸も速いため自
動車産業を中心に広く使用さnていゐ。しかしアルミ鋳
物のような鋳込み湯度の低い鋳型に用いた場合には,鋳
型の崩壊性が悪く500℃位の面部で6〜12時間も力
I]熱処坤を必按としており鋳込み候の砂落し作業に非
常に太@な費用と労力が必要となっている。そこで鋳型
の崩壊性忙改良丁るkめに鋳物川砂にポリイソシアネー
トとポリオールを配会しアミンカスで硬化ざ一+!:ゐ
方法が一発ざれlcがアミンカスのa性や英気対策に問
題がある。又鋳物川砂にポリインシアネートとアミン系
ボリオールを配会し、目映化性の崎型R埴刀砧が開発さ
れ′fcが級化すゐ′まで長時間たかる問題がある。
Conventionally, there have been numerous processes for manufacturing limited quantities, but the shell molding method has been used in the automobile industry for phenolic resins because it has excellent dimensional stability of the mold, good mold skin, and quick curing. Widely used in the center. However, when used in a mold with a low pouring temperature such as an aluminum casting, the mold has poor disintegration properties and requires heat treatment for 6 to 12 hours at a surface temperature of about 500°C, which prevents the mold from pouring. Sand removal work requires a huge amount of cost and labor. Therefore, in order to improve the disintegration of the mold, polyisocyanate and polyol were added to the foundry river sand, and it was hardened with amine scum! :2 The method is one shot, and LC has a problem with Aminekasu's agility and energy countermeasures. Furthermore, a highly visible Saki-type R Hanito-Kinto was developed in which polyincyanate and amine-based polyol were added to foundry river sand, but there was a problem in that it took a long time until the ``fc'' was graded.

そこで鋳物莱界〃・らシェルモールド法と隣1様Zl’
f条c/)できかつ鋳型の崩壊性が凌扛ていゐ躯テ〃の
製電方法の開発が強く俊望されている。
Therefore, the casting Raikai shell mold method and the next one Zl'
There is a strong demand for the development of a method for producing electricity that can be produced using the following methods:

本発明、tl−は鈎込み俊加熱処理ケ低減し容易にし。In the present invention, TL- reduces and facilitates heat treatment.

崩壊ぢかつ現行のシェルモールド法とI’JQ’Pの作
条のできる鋳型の製社方法について鋭意検討した結朱鋳
物用砂にブロックイン/アネート化合物とンゾール型フ
ェノール樹脂を含有する組成物を伝堕しに薮恨砂をカD
熱により級化させて駒型?ll″装迫丁ゐことにより鋳
込み俊の崩壊性が著しく改善芒れ、刀為つ現行のシェル
モールド法と回等の11−菜(砂の流動性、硬化速度)
ができゐことを見い出した。
A composition containing a block-in/anate compound and a resin-type phenolic resin was added to the foundry sand, which was developed by intensively studying the current shell mold method and the manufacturing method of molds that can produce I'JQ'P strips. Kad Yabusa for the downfall
Is it graded by heat and shaped into pieces? The disintegration properties of the cast molding have been significantly improved by using the molding method, and the current shell molding method and 11-item (fluidity of sand, hardening speed)
I discovered that it is possible.

丁なわち不発明によれは上記がらな;bi3物用樹脂破
6を砂を150℃〜650 ℃に加熱δ扛だ金型に元J
IXちせゐと、ブロックィンンアイ・−ト化合物のブロ
ック沖」がル41#lルし1発生丁ゐインシアネート化
合9勿とレン°−ル型フェノール1m(Mkのメチロー
ル基及び水酸基等が反応しウレタン結合により鋳型が強
固[なり抜型可能な強度に堰丁ゐ。又鋳型の崩壊性が著
しく同上する。Cれは鋳型の形成にウレタン結合を用い
ているためと思われる。
In other words, according to the invention, the above is the same; sand is heated to 150°C to 650°C, and the mold is heated to 650°C.
IX chisei and the block oki of the block-in-a-to compound are 41 #1 generated in cyanate compound 9, and 1 m of lene-type phenol (the methylol group and hydroxyl group of Mk are The mold becomes strong due to the urethane bond that reacts and becomes strong enough to be removed from the mold.Also, the mold collapses significantly.It is thought that the cracking is due to the use of the urethane bond in forming the mold.

本発明に用いる組成物のブロックイソシアネート化合物
とじてはポリインンアネート化合吻とインシアネートブ
ロックハリとの付加反応生成物が用いられゐ。ポリイン
シアネート化合′吻としてFI[米公知のインシアネー
トか〒2個以上有丁ゐインシアネート化合物のいずれも
使用することがでさ、又、これらのポリイソシアイ・−
ト化合物とエチレングリコール、グロビレングリーy−
ル、ト!jメテロールプロハ/、グリセリン、ポリエー
テルポリオール耕などの活性水素化付物などと1反比−
させた末端インシアネート基貧有化合物なども用いられ
る。
The block isocyanate compound used in the composition used in the present invention is an addition reaction product of a polyinyanate compound and an incyanate block. As the polyisocyanate compound, FI [any of the incyanate compounds known in the United States or the incyanate compounds having two or more atoms can be used, and these polyisocyanates -
compounds and ethylene glycol, globylene glycol
Le, to! 1 opposite ratio to active hydrogenated adducts such as metherol proha/, glycerin, and polyether polyol.
Compounds containing terminal incyanate groups may also be used.

インシアネートブロックAllとしては、従来より用い
ら扛ていゐものは吟ず牡も使用′Tゐことができ、フェ
ノール、クレゾール、キシレノール、ノニルフェノール
等の7エ/−ルXtt−ブチルアルコール等の第6殺ア
ルコール知、アセナルアセトン、マロン醒ジエステルな
どの活性メチレン化舎*、メナルアニリン、ジンエニル
アばンlどの芳香族アミン類、フタル販イミドなとのイ
ミド湘、ε−カブロシクタムなどのラクタム類、エチレ
ンイミンなどのイミン類。
As the incyanate block, it is possible to use not only those that have not been used conventionally, but also seven alcohols such as phenol, cresol, xylenol, and nonylphenol. Active methylene compounds such as alcoholic acid, acenaracetone, and malonated diesters, aromatic amines such as menalaniline and ginylamine, phthalate imides, lactams such as ε-cabrocyctam, and ethylene imine. imines such as

尿索殖、オキシム鎚、産血饋敵塩頬、ホウ酸類などがあ
る。不発明にハjいゐブロックィソンアネート化合q/
Jは上記イソシアネート化曾1勿と1ンシアネートブロ
ソク化納とt促米公知の方法によ!ll戊応芒ぜて侍ら
tゐ。
There are urinary tracts, oxime hammers, urinary tracts, and boric acids. Blockison anate compound q/
J is obtained by the above-mentioned isocyanate conversion method, the isocyanate conversion process, and the known method. The samurai will respond.

父1本発明に用いるVゾール型フェノール伺脂としては
砂の&悪注保付のためビスフェノール漬を用いたレゾー
ル化j)財が好ましく丈に布齢で固形のものが好ましい
0レゾールυフエノールうη(8旨としては、メチロー
ル基tもっ7j 7 、r−ノール)lE jD、fで
あ扛はいずれでも使用丁ゐことができ又レゾール型フェ
ノール伺廁の合成についても府に限定しないがフェノー
ル、クレゾール。
Father 1 The V-sol type phenol resin used in the present invention is preferably a resol using bisphenol pickling for sand & dirt retention. η (for example, methylol group 7j 7 , r-nol) lE jD, f can be used in any form, and the synthesis of resol-type phenol is not limited to phenol. , cresol.

ビスフェノールA1 ビスフェノールS、ビスフェノー
ルF=4.のフェノール頬とホルムアルデヒドをNaO
H,Ba(OHル、アンモニア、トリメチルアミン等の
合成触媒を用いて反比1δぜ促米公知の方法によりイ4
らオする0レゾール型ビスフェノールiD、(ahとじ
てげ、ビスフェノールへ、ヒスフェノールS1 ビスフ
ェノールF号のビスフェノール類とホルムアルデヒド’
z lNaOH,Ba(OH%アンモニア、トリメチル
アミン寺の触媒τ用いて反応さぜゐことにより伯られゐ
憫bbが用いらf′Lゐ0 レゾール型ビスフェノール側j財としてビスフェノール
A1壬ルVC均してホルムアルデヒドは1.5〜4.0
モルを反応はせて侍られ勾4LljIIばか好1しく用
いら7シイ。ホルムアルデヒドか1.5モル未満である
とメチロール産が少なく191II!!化速反が遅くl
り、又ホルムアルデヒドが4.0モル全越えると砂型の
)JD熱映化時eCホルムアルテヒド臭が強くなり好ま
しくない。
Bisphenol A1 Bisphenol S, Bisphenol F = 4. Phenol cheeks and formaldehyde of NaO
Using a synthetic catalyst such as H, Ba (OH, ammonia, trimethylamine, etc.)
0 resol-type bisphenol iD, (ah tojitege, to bisphenol, hisphenol S1 bisphenol F No. bisphenol and formaldehyde)
z lNaOH, Ba (OH% ammonia, trimethylamine) is reacted using a catalyst τ. Formaldehyde is 1.5-4.0
The mole is reacted and served, and the gradient 4LljII is preferably used. If formaldehyde is less than 1.5 mol, methylol production will be low and 191II! ! The rate of reaction is slow
Furthermore, if the total amount of formaldehyde exceeds 4.0 moles, the odor of formaldehyde will become strong during JD thermal imaging of the sand mold, which is not preferable.

本発明に用いられる鋳物用クチ脂被核砂に、90〜18
0℃に加陥されにμj物用用砂固形あるいIrl m 
a(1)ブロックインシアネート化合物とレゾール型フ
、ノール仙j脂(1−攪拌混合せしめ、この重付工程中
に必貴VC応し俗媒τ蒸発ぜしめゐことによりイむら扛
ゐ。鋳物砂の温度が180’Cを悲えるとプロソタイソ
シアネート化合’IyAの解離が鮒なりa’j勿月〕位
」用イ仮イ艮侠のライフが短かぐなりijかりT″なく
砂型の頻度も低1し好なしくない。又温度が90℃未満
の揚台、樹脂の扱軸が不十分となったり浴媒の魚介〃・
不十分となりη物用@脂扱抜妙の1独7一点か低くなり
プロノキングズ匙こ丁ので好ましくない。
90 to 18
When heated to 0°C, μj material sand solid or Irl m
a(1) Blocked incyanate compound and resol-type resin (1) are stirred and mixed, and during this weighting step, the necessary VC and the common medium τ are evaporated to increase the uniformity.Casting. When the temperature of the sand reaches 180'C, the dissociation of the prosotysocyanate compound 'IyA' becomes a carp, and the life of the character is shortened and the frequency of sand molding is reduced. Also, the temperature is lower than 90℃, the handling axis of the resin is insufficient, and the bath medium is not good.
It's not good enough, and it's 1, 7, or 1 point, which is unfavorable for Prono Kings.

又用いるブロックインシア子−ト化合物とレン゛−ル邪
フェノール4fl I!旨の凸己台割合(厘童比)(り
95:57111ら5:95の馳凸で用いら扛好葦しく
は85:、157)−ら5〇ニア0の単巳四でハ」いら
れる。ブロックイソシアネート化合物か多丁さゐと硬化
が遅くなり又レゾール型フェノール側j4μか多丁きる
と砂型のノリj壊性か恋(なゐ。
Also used are blocked incyate compounds and phenol 4fl I! The convex ratio of the ratio (Rindou ratio) (R95:57111 and 5:95 is used in the hase convexity is 85:, 157) - 50 near 0 in the single-legged four. It will be done. If the block isocyanate compound is used too many times, the curing will be slow, and if the resol type phenol side is used with 4 μm or more, the sand mold glue will be destroyed.

父病型をIR迫する時の加熱温区は150’C;〜65
0℃でφゐ。150℃未64″′Cψ心と組成の硬化が
遅くなり、650℃ビ越えゐと鉄4の強要が低下し1ζ
り$b席の肌か悲〈なゐ弄の入点がめゐ0 砂と混付し扱復丁な組成物子のプロツタ1ソシア不−ト
化合物とレゾール型フェノール側(11百〇付酎童は鋳
物川砂に対して乙0〜0.6里炬ジbでりり好’EL(
は6.0〜0.5皿け%でりゐ。6加すゐ梗脂台計童が
7%ケ越えるとし゛、j物製足吋のカス欠陥の原因とな
るだけでなく 1+ft+伯も市(な9よくない。又0
,5%木滴でめゐと砂型の頻度か低くなV実用Vc1針
えない。
The heating temperature range when applying IR for the father's disease type is 150'C; ~65
φゐ at 0℃. Below 150℃, the hardening of the 64''Cψ core and the composition slows down, and above 650℃, the coercive force of iron 4 decreases and 1ζ
The skin of the $b seat is a shame. is 0 to 0.6 ri for casting river sand.
The percentage is 6.0 to 0.5%. 6. If the amount of 6% added to the fat base exceeds 7%, it will not only cause defects in the foot of the product, but also cause 1 + ft + weight (9 not good. Also 0
, With 5% wood droplets, the frequency of sand molding is low, and Vc1 needles cannot be used for practical purposes.

又、本発明で侍らtした防吻用但j狛扱楓砂に便米公刈
のブロックインシア子・−ト化合物の屏陥肛殊のいずれ
も反相できジブチルチンジラウレート、塩化第2スズ、
ナンテンばコバルト咎を硲ガロしてもよ(崩好の一7I
II払に捌廂薗形分に対しo、 0 + 〜1.0 生
w%−cある。
In addition, in the present invention, the anti-proboscis used in the treatment of maple sand can be used to block infiltration of the compound of dibutyl tin dilaurate, stannic chloride, etc. ,
Nanten, even if you blame Cobalt, please (Kurokoichi 7I)
In II payment, there is o, 0 + ~ 1.0 raw w%-c for the part of the kanji.

又、 胸管ノ用佃」1」旨扱gイレi’(: Ui;動
1土足すと女すにするために7エルモールド法で刀jい
られているステアリンを波カルシウムのよ′)な滑AI
Jt師加しても又、鋳吻用倒脂被榎砂台装這簿挟丁ゐ除
に。
In addition, the thoracic tube's use of ``1'' is treated as ``1'' (: Ui; the stearin that is used in the 7 Hermold method to make it a woman's body is a wave of calcium). Nalu AI
Even if Jt is added, it will also be necessary to remove the sand plate mounting plate for casting proboscis.

フロックインシアネート化合9勿とレゾール型フェノー
ル樹脂の混合方法は特に限定するものでなく、砂と撹拌
混合丁ゐ前に両奴分て予め混合していても父、混脅時に
別々に投入してもよい。
There are no particular restrictions on the method of mixing the flocked incyanate compound 9 and the resol type phenolic resin. Good too.

又本発明で用いる鋳物川砂としては通常νj物用に使用
しているものはいずれでもよくジルコン砂、オリピン砂
も1更用でさる。
The foundry river sand used in the present invention may be any of those normally used for νj materials, and zircon sand and oripin sand can also be used in one step.

以下不発明の冥hIII例を示す。An example of the uninvented Mei hIII is shown below.

実施例1 (レゾール型フェノール樹脂の合flC)還流冷却器奢
916見つけた4つロフラスコにビスフェノールA22
80g57%ホルマリン1620gを投入し20%Na
OH水ai40gを姉加し還流温度で2時間反応させた
俊脱水磯粗ケ行ない固状樹脂が侍し扛だ〇 (鋳物用・萌脂扱恒砂の製迫法) 混線機に160℃に力ロ熱したフッタ1ノー珪砂8kg
Kコロネー)APステーブル(H本ボ1ノウレタン社製
、フエ・ノールでマスクされたイソシアネート化合物、
軟化点的100”C)120gと上記で倚らtたレゾー
ル型フェノール側+1illTb40gを力pえて砂が
崩壊丁/)丘で撹拌ン昆合丁ゐ0その佼ステアリン威カ
ルシウム8g’、L’7JDχ史に20秒間混合し餉物
用側崩複核砂か侍られた0砂型吋性を堀−I VC示す
0 実施例2 ?M、1aeK’110°Cic 7JD PA シf
c 771 !J *e8kgにコロネートAPステー
プル100gとアセトン60gからなゐ浴液と実施例1
で1好られたレゾ−ル型フェノール側 ン60gからな/)浴液を力【1χて砂が崩壊丁ゐ筐で
攪拌混合する0その俊ステアリン醒カルシウム8gを加
え具に20秒間混合し、錫)’IIIJ用イ立■ハu′
fL榎砂が得られた0砂型特注ケ表−1にが丁0実施?
l15 混#l[160℃に加熱したフラタ1ノー珪砂8 kg
 K りL/ 5ンクロスリンキングエイジエント・U
T(住人バイエルウレタン社製、ε−カプロラクタムで
マスクされたインシアネート化合物、軟化点朽+ 00
℃) 100 gk7JVLc40秒m件混合した候失
施例1で傅ら′t′したレゾール型フz / −k4A
4ノj’# 60 gとメタノール30gZ+aらZゐ
浴液を力nえて砂が崩壊Tるまで侃件混合丁ゐ。
Example 1 (Synthesis of resol type phenolic resin) Bisphenol A22 was placed in a four-bottle flask with a reflux condenser 916.
Add 80g 57% formalin 1620g and 20% Na
Add 40 g of OH water and react at reflux temperature for 2 hours to obtain a solid resin. Powerfully heated footer 1 no silica sand 8kg
K Coronet) AP Stable (manufactured by H Honbo 1 Urethane Co., Ltd., isocyanate compound masked with phenol,
Softening point: 100" Mixed for 20 seconds and mixed for 20 seconds, the 0 sand type sand was mixed with Hori-I VC.
c771! J*e 8 kg, 100 g of Coronate AP staples, and a bath solution consisting of 60 g of acetone and Example 1
1. Add 8 g of dissolved calcium stearin and mix the bath solution for 20 seconds with stirring in a container until the sand collapses. Tin) 'IIIJ for I stand ■ Ha'
Is the 0 sand mold custom made table 1 where fL Enoki sand was obtained?
l15 Mixed #l [8 kg of flata 1-no silica sand heated to 160°C
K Ri L / 5 N cross linking agent U
T (manufactured by Bayer Urethane GmbH, incyanate compound masked with ε-caprolactam, softening and disintegration + 00
℃) 100 gk7JVLc40 secondsm mixed defect Example 1 resol type fuz / -k4A
Mix 4 pieces of 60 g of methanol and 30 g of methanol with the bath liquid until the sand collapses.

その欽ステアリ7ばカルシウム81Zf1:)Mえ史ニ
20秒向混付し駒吻用倒脂被し砂が得られた。
The mixture was mixed in the same direction for 20 seconds to obtain sand covered with fat.

砂型特性を表−1Vc示す。Table 1Vc shows the characteristics of the sand mold.

実施例4 ジブチルチンジラウレート 以外は実施例6とIO2様にて勿物用街カa被様砂が得
らfした。砂型特性7表−1に示す。
Example 4 Except for dibutyltin dilaurate, sand was obtained using the same methods as Example 6 and IO2. Sand mold characteristics 7 are shown in Table-1.

比較例1 (ノボンック型フェノールイ17J I釘の8171 
)層流冷却器を備えつけた4つロンラスコにフェノール
1880g。57%ホルマリン244g.80%パラホ
ルムアルデヒド488gを投入しシュウ酸4g?r硲〃
口し還。11菱で5時間反応させに俊脱水り#縮を行な
い固状tiLI脂が傅ら扛た0 (鋳物用樹脂被恨砂の製造) 混練機に160℃VC加熱したフラタリー址砂8kgに
上B已で倚らnlcノホラック披フェノール側脂樹脂0
g全力口えて40秒li−iI撹拌混会した俵へキサメ
チレンテトラミン24gと7XdOg77為らなゐ浴液
を力口χて砂が崩敲丁ゐまで偉拌混台丁ゐ0その俊ステ
アリン敵カルシウム8gτ加え史[20秒間混付し餉物
用側胎扱後砂炉憎られた。砂型物性を表−IK示す。
Comparative Example 1 (Novok type phenol 17J I nail 8171
) 1880 g of phenol in a 4-long lasco equipped with a laminar flow condenser. 57% formalin 244g. Add 488g of 80% paraformaldehyde and 4g of oxalic acid? r 硲〃
Talk back. After reacting for 5 hours in a No. 11 machine, the solid TiLI fat was removed by quick dehydration and #condensation. NLC Noholac Phenolic Resin 0
Stir with all your might for 40 seconds, pour 24g of xamethylenetetramine and 7XdOg77 into the mixed bales, and mix vigorously until the sand crumbles. Add 8 g of calcium and mix for 20 seconds. Table IK shows the physical properties of the sand mold.

比較例2 混練イ女VC160℃に力1熱した)2タリ一珪伏8k
gVCコロネートAP,z.テーブル100gと比較例
1で侍らnπノボラック型フェノール街脂60gケカロ
えて砂が崩壊丁ゐまで1に件混台丁ゐ。
Comparative Example 2 Kneading VC (heated to 160℃)
gVC Coronate AP, z. Using 100g of table and Comparative Example 1, 60g of nπ novolac type phenol street resin was mixed until the sand collapsed and the mixture was mixed.

その後ステアリン戚カルシウム8gt7IIJえ史に2
0秒間混合し、鋳物用便舶被薇砂が侍らnた。
After that, stearin relative calcium 8gt7IIJ Eshini 2
Mix for 0 seconds and pour out the foundry sand.

砂型物性を表−IK挙丁。The physical properties of the sand mold are listed below.

比較例6 混練機に110℃に加熱したンラタリー珪砂 本8 K
g ic :y oネートAPステープ#10[1gと
ア七トン60gからなる溶液とサンニソクス)] S−
20y’(三洋化成工栗社表,シュクローズ糸ポリオー
ル粘度約7 0 PI3 5℃)sagとア七トン5 
0 g77・らl/)俗l灰を加えて6分1dJ混台し
π妙ステアリン敵カルシウムBgk)JDχ更に20秒
曲混合し鋳物用樹脂扱榎砂が侍らtL 7c (。
Comparative Example 6 Nratari silica sand heated to 110°C in a kneader 8K
g ic:yonate AP tape #10 [a solution consisting of 1g and 60g of acetone and sannisox)] S-
20y' (Sanyo Kasei Kokuri Co., Ltd., Sucrose yarn polyol viscosity approximately 70 PI3 5℃) sag and A7ton 5
0 g77・ra l/) Add ash and mix for 1 dJ for 6 minutes. π Stearin Enemy Calcium Bgk) JDχ Mix for another 20 seconds.

砂型特性勿軟−1に示す〇 *・ *1 曲け”jMe ’ J I S K 6 9 1
 0法Vc テ#4w*2 融治点 二JACT法にて
徂1]泥GQ− 6 砂型崩壊i:250℃に加熱し7j30φX5om
nlHの金型に鋳物用便Bk僚稙砂を入れ400”C電
気炉中で6分間硬化させテストピースを作成する。無散
系状匹に仙ζった500’Cにカロ熱しに金型に刺入し
500℃炉中で20分間焼成した俊放冷丁ゐ。
Sand mold characteristics: Softness - 1 as shown in 〇*・ *1 Bending"jMe' JIS K 6 9 1
0 method Vc Te#4w*2 Melting point 2 JACT method 1] Mud GQ-6 Sand mold collapse i: Heated to 250℃ 7j30φX5om
A test piece is prepared by putting foundry sand in a NLH mold and curing it for 6 minutes in a 400"C electric furnace. Heat the mold to 500'C in a non-dispersible state. Shunpō Reitōi is baked in a 500°C oven for 20 minutes.

このテストピースを28メツシユのフルイにのせロータ
ツブ2ルイ振とシ慎葡用いて1分IijJ振と9しその
減少足から次式により崩駁率勿求めた04 ベンド :
副定渦l建にセットした平板金型70X1 4 0 [
111+1J:頃工=ヨJ金讃内寸5 0 X 1 2
 QInJ[1δ5mmt直さ一Jす勿用位J脂扱俵砂
釦光塙したものt炉筒650℃内ic40秒放直しその
鋏と9出し10秒後に支点間距離IQQm+nの付臭上
に直さ500g向里をかけたときのたわみ量を測足しk
O低繍でたわ4倉の少ないものは級化が速いことt慧味
する。
This test piece was placed on a 28-mesh sieve, and the rotor tab was used for 1 minute of IijJ and 9 strokes using a rotor tube of 2 and 2.
Flat plate mold 70X140 set in sub-constant vortex l building
111+1J: Koroku = YoJ Kinsan inner dimension 5 0 X 1 2
QInJ [1 δ 5 mmt Straighten 1 J Suitable position J Fat handling bale Sand button light sill t Furnace cylinder 650℃ IC 40 seconds and then scissors 9 out After 10 seconds, straighten 500 g on the odor with distance between fulcrums IQQm + n Measure the amount of deflection when multiplied by k
It is advantageous that items with low embroidery and a small number of weights and weights are quickly graded.

本発明による鋳型の裟迄刀法ケ用いることによ、す、シ
ェルモールド法と同等の砂のvit 5tJJ a s
砂型の硬化速度がありかつ鋳型の崩敬性に優れた躯!ム
リか侍られゐ0 一1武q−
By using the molding method according to the present invention, it is possible to create a sand mold equivalent to the shell mold method.
A structure that has the hardening speed of a sand mold and has excellent mold collapse resistance! Is it impossible to serve you?0 11 Takeq-

Claims (1)

【特許請求の範囲】 1、鋳物川砂にブロックインシアネート化会物とレゾー
ル型フェノール伺脂を含有丁ゐ#i底物を複核した鋳物
用樹脂被核砂をカロ熱により硬化させることt%敬とす
る鋳型の#愈万び。 26 レゾールmフェノール樹脂がレゾール〃ビスフェ
ノール御脂であることt脣畝とする府でホルムアルデヒ
ド1.5〜4.C1モルを反応ざぜて倚らtゐイ釘脂で
あること全特徴とする付r[請求の範囲第1項又は第2
墳gt載の鋳型の製造方法。 4、加熱の自[が150℃〜550 ℃であることをL
Ff倣と′Tる脣許請求の範囲第1項記載の@型の製造
方法。
[Scope of Claims] 1. Hardening of foundry resin enucleated sand containing block incyanate compound and resol-type phenol resin in foundry river sand using Calothermal heat. #Yumanbi of the mold. 26 The resol m phenolic resin must be a resol bisphenol oil with a formaldehyde content of 1.5 to 4. [Claim 1 or 2]
A method for manufacturing a mold for mounting a tomb. 4. Make sure that the heating temperature is between 150℃ and 550℃.
A method for manufacturing an @-type according to claim 1, which includes Ff copying.
JP15935283A 1983-08-31 1983-08-31 Production of casting mold Granted JPS6049830A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15935283A JPS6049830A (en) 1983-08-31 1983-08-31 Production of casting mold

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15935283A JPS6049830A (en) 1983-08-31 1983-08-31 Production of casting mold

Publications (2)

Publication Number Publication Date
JPS6049830A true JPS6049830A (en) 1985-03-19
JPS6261375B2 JPS6261375B2 (en) 1987-12-21

Family

ID=15691965

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15935283A Granted JPS6049830A (en) 1983-08-31 1983-08-31 Production of casting mold

Country Status (1)

Country Link
JP (1) JPS6049830A (en)

Also Published As

Publication number Publication date
JPS6261375B2 (en) 1987-12-21

Similar Documents

Publication Publication Date Title
CN106046283B (en) High ortho position benzylic ether phenolic resin, preparation method and applications are in the method for cold-box binder
WO2009150983A1 (en) Manufacturing method for phenolic novolac resin and resin‑coated sand
US3838095A (en) Foundry sand coated with a binder containing novolac resin and urea compound
US2856381A (en) Foundry sand binder composition containing at least three phenol-formaldehyde resins
JPS6049830A (en) Production of casting mold
EP0007686A1 (en) A method for preparing a novolak phenol-formaldehyde resin, a method for making resin coated granules for foundry moulding and a foundry mould component made from the granules
US3944510A (en) ABS-formaldehyde novolak
US3644269A (en) Collapsible mold and molding compositions
US4370463A (en) Process for no-bake foundry application utilizing polyurethanes based on amine polyols
WO1988008763A1 (en) Hot box process for preparing foundry shapes
CA1203439A (en) Shell-molding resin coated sand
JPS63101038A (en) Production of resin coated sand grain for shell mold
JPS5846377B2 (en) Binder composition for foundry sand
JP5549830B2 (en) Resin coated sand using phenolic novolac resin
US4459375A (en) Resin coated sand for shell foundry process
US3816558A (en) Filled aldehyde condensates having improved heat resistance
JPS6049829A (en) Resin-coated molding sand curable by heating and its production
JPS6114043A (en) Resin-coated sand curable by heating for casting and its production
JPS62151240A (en) Production of resin for casting curable by heating
JPS6116213B2 (en)
US2915491A (en) Phenolic resins and their use in moulding processes
JPS6114042A (en) Production of casting mold
US1717614A (en) Phenolic resin and process of making the same
JPS6055543B2 (en) Thermosetting phenolic resin composition
JPS6393442A (en) Resin binder for shell mold