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JPH04123836A - Binder composition for molding sand - Google Patents

Binder composition for molding sand

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Publication number
JPH04123836A
JPH04123836A JP24072590A JP24072590A JPH04123836A JP H04123836 A JPH04123836 A JP H04123836A JP 24072590 A JP24072590 A JP 24072590A JP 24072590 A JP24072590 A JP 24072590A JP H04123836 A JPH04123836 A JP H04123836A
Authority
JP
Japan
Prior art keywords
acid
resin
salt
composition
aldehyde
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
JP24072590A
Other languages
Japanese (ja)
Other versions
JP2831826B2 (en
Inventor
Hajime Murayama
肇 村山
Minoru Maeda
実 前田
Shigeo Nakai
茂夫 仲井
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.)
Kao Corp
Original Assignee
Kao Corp
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 Kao Corp filed Critical Kao Corp
Priority to JP24072590A priority Critical patent/JP2831826B2/en
Publication of JPH04123836A publication Critical patent/JPH04123836A/en
Application granted granted Critical
Publication of JP2831826B2 publication Critical patent/JP2831826B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To drastically improve the smoothness of casting surface by specifying the composition of acid-setting resin used for binder for molding sand. CONSTITUTION:The binder composition for molding sand is composed of the acid-setting resin and strong acidic salt and weak basic salt and used at the time of forming a mold by kneading this with refractoriness granular aggregate and heat-setting this, and having the following characteristic composition in the acid-setting resin (a) 20-35wt% resol type phenol resin, (b) 40-65wt% furfuryl alcohol or furan resin, (c) 15-30wt% keton resin composed of at least one kind of cyclohexanone, cyclopentanone or aromatic keton and aldehyde and 1:1-1:3mol ratio of the keton to the aldehyde.

Description

【発明の詳細な説明】 (産業上の利用分野〕 本発明は加熱硬化製造法によって鋳型を製造する際に用
いられる鋳物砂川粘結剤組成物に関するものである。更
に詳しくは、酸硬化性樹脂と硬化剤からなり、耐火性粒
状骨材に混練してこれを加熱硬化させて鋳型を得る際に
用いられる鋳物砂川粘結剤組成物に関するものである。
Detailed Description of the Invention (Industrial Field of Application) The present invention relates to a foundry Sunagawa binder composition used when manufacturing molds by a heat curing manufacturing method. The present invention relates to a casting Sunagawa binder composition, which consists of a hardening agent and a refractory granular aggregate, and is used to obtain a casting mold by kneading it into a refractory granular aggregate and curing it by heating.

〔従来の技術及びその課題〕[Conventional technology and its problems]

従来、加熱硬化鋳型の製造法としては、耐火性粒状骨材
にフェノールノボラック樹脂を被覆し、ヘキサメチレン
テトラミンを触媒として加熱硬化せしめる、所謂フェル
モード法がある。
Conventionally, as a method for producing heat-cured molds, there is a so-called Fermode method in which a refractory granular aggregate is coated with a phenol novolak resin and heated and cured using hexamethylenetetramine as a catalyst.

この加熱硬化法は設備的に簡便であり、作業的に使用し
易い等の利点により現在加熱硬化鋳型製造法としては最
も多く使用されている。しかしながら、硬化時間が長く
、硬化温度が高い為、金型の歪み、鋳型の歪みが多く、
鋳型のハリ取り作業が欠かせず、また寸法精度も不充分
であった。更に硬化温度が高い事による作業環境の劣悪
さ、及びフェノール樹脂とへキサメチレンテトラミンの
熱分解臭気による作業環境の汚染も著しく、これらの大
幅な改善が望まれていた。
This heat-curing method is currently the most commonly used method for producing heat-curing molds because of its simple equipment and ease of use. However, due to the long curing time and high curing temperature, there is a lot of distortion in the mold and mold.
It was necessary to remove the tension from the mold, and the dimensional accuracy was also insufficient. Furthermore, the working environment is poor due to the high curing temperature, and the working environment is extremely polluted due to the odor of thermal decomposition of the phenol resin and hexamethylenetetramine, and a drastic improvement in these conditions has been desired.

また、250°C付近で耐火性粒状骨材にフェノールレ
ゾール樹脂やフラン分の少ないフェノール又は尿素/ホ
ルマリン変成フラン樹脂等の酸硬化性樹脂と、塩化アン
モニウム、ンユウ酸等の硬化触媒との混合物を加熱硬化
させる、所謂ポットボックス法が有る。これは硬化時間
もシェルモールド法よりは短く、温度による歪み、寸法
精度や熱的作業環境の面でも改善されるが、更に硬化時
間の短縮、鋳型の物性向上、作業環境の改善が望まれて
いる。
In addition, a mixture of acid-curing resins such as phenol resol resin, phenol with low furan content, or urea/formalin-modified furan resin, and a curing catalyst such as ammonium chloride or sulfuric acid is added to the refractory granular aggregate at around 250°C. There is a so-called pot box method in which the material is cured by heating. This method also has a shorter curing time than the shell mold method, and improves distortion due to temperature, dimensional accuracy, and thermal working environment, but it is desired to further shorten the curing time, improve the physical properties of the mold, and improve the working environment. There is.

これらに対して耐火性粒状骨材に酸硬化性樹脂及び硬化
剤としての強酸と弱塩基の塩からなる粘結剤を混合した
混合物を200°C付近の比較的低温で加熱硬化させる
、所謂ウオームボックス法は前記の難点を解決する方法
として近年急速に注目を集めている。
In contrast, a so-called worm method is a method in which a mixture of fire-resistant granular aggregate, an acid-curable resin, and a binder consisting of a salt of a strong acid and a weak base as a hardening agent is heated and hardened at a relatively low temperature of around 200°C. The box method has been rapidly attracting attention in recent years as a method for solving the above-mentioned difficulties.

〔発明が解決しようとする課題] ウオームボックス法は、鋳型製造時の省エネルギー効果
が高いこと、鋳型製造速度が速いこと、製造された鋳型
の品質が優れること、製造された鋳物の内部欠陥が少な
いこと等、従来のシェルモールド法、ホントボックス法
より優れた数々の特徴を有するが、製造された鋳物の表
面粗度、所謂鋳肌がやや劣っており、この点を改善する
ことが望まれている。
[Problems to be solved by the invention] The warm box method has a high energy saving effect during mold manufacturing, a fast mold manufacturing speed, excellent quality of the manufactured molds, and few internal defects in the manufactured castings. However, the surface roughness of the manufactured castings, the so-called casting surface, is somewhat inferior, and it is desired to improve this point. There is.

本発明は、ウオームボックス法の特徴を生かしつつ、製
造された鋳物の表面粗度、所謂鋳肌の改善が達成される
鋳物用粘結剤組成物を提供することを目的とする。
An object of the present invention is to provide a binder composition for castings that can improve the surface roughness, so-called casting surface, of manufactured castings while taking advantage of the characteristics of the warm box method.

ウオームボックス法において鋳肌の滑らかさを左右する
要因としては、 ■ 鋳型の充填密度などの造粒技術面での要因■ 使用
する耐火性粒状骨材の粒度・材質等の要因 ■ 鋳物用粘結剤組成物が熱分解時に発生するガス組成
などの粘結剤面での要因 等が挙げられる。
The factors that affect the smoothness of the casting surface in the warm box method include: ■ Factors related to granulation technology such as the packing density of the mold ■ Factors such as the particle size and material of the refractory granular aggregate used ■ Caking for castings Factors related to the binder include the gas composition generated when the agent composition is thermally decomposed.

これらの要因のうち、造型技術面においては種々検討が
なされているが、鋳型や造型機の違いによる制約も多く
、実用化は困難である。また、骨材面では粒度、材質が
鋳物の鋳肌以外の諸性質にも大きな影響を与える等の制
約があり、やはり実用化は難しい。それ故、上記課題に
対し、粘結剤面からの改善が強く要望されているのが現
状である。
Among these factors, various studies have been made in terms of molding technology, but there are many restrictions due to differences in molds and molding machines, making it difficult to put them into practical use. Furthermore, in terms of aggregate, there are restrictions such as particle size and material that have a large effect on various properties other than the casting surface of castings, so it is still difficult to put it into practical use. Therefore, in order to solve the above problem, there is currently a strong demand for improvement from the viewpoint of binders.

〔課題を解決するための手段〕[Means to solve the problem]

本発明者らは、鋭意研究の結果、ウオームボックス法に
おいて、用いられる粘結剤にシクロヘキサノン、シクロ
ペンタノン及び芳香族ケトンから選ばれた少なくとも1
種のケトンとアルデヒドからなりケトン対アルデヒドの
モル比が1:1〜1:3のケトン樹脂を含有させること
で、製造される鋳物の鋳肌が大幅に改善されることを見
出し、本発明を完成するに至った。
As a result of intensive research, the present inventors have found that at least one binder selected from cyclohexanone, cyclopentanone, and aromatic ketone is used in the warm box method.
It was discovered that the casting surface of manufactured castings was significantly improved by incorporating a ketone resin consisting of a ketone and an aldehyde with a molar ratio of ketone to aldehyde of 1:1 to 1:3, and the present invention was developed based on this discovery. It was completed.

即ち、本発明は、酸硬化性樹脂、及び強酸と弱塩基の塩
からなり、耐火性粒状骨材に混練してこれを加熱硬化さ
せることにより鋳型を成型する際に用いられる鋳物砂川
粘結剤組成物であって、前記酸硬化性樹脂が下記の組成
を有することを特徴とする鋳物砂川粘結剤組成物を提供
するものである。
That is, the present invention is a foundry Sunagawa binder, which is made of an acid-curable resin and a salt of a strong acid and a weak base, and is used when molding a mold by kneading it into a fire-resistant granular aggregate and curing it by heating. The present invention provides a foundry Sunagawa binder composition, wherein the acid-curable resin has the following composition.

(a)レゾール型フェノール樹脂  20〜35重量%
(b)フルフリルアルコール又はフラン樹脂40〜65
重量% (c)シクロヘキサノン、シクロペンタノン又は芳香族
ケトンの少なくとも1種とアルデヒドからなりケトン対
アルデヒドのモル比が1:1〜1:3のケトン樹脂  
  15〜30重量%木発明に用いられる酸硬化性樹脂
はレゾール型フェノール樹脂、フルフリルアルコール又
はフラン樹脂、並びにシクロヘキサノン、シクロペンタ
ノン及び芳香族ケトンから選ばれた少なくとも1種のケ
トンとアルデヒドがらなリケトン対アルデヒドのモル比
が1:1〜1:3のケトン樹脂を含有する。
(a) Resol type phenolic resin 20-35% by weight
(b) Furfuryl alcohol or furan resin 40-65
Weight % (c) A ketone resin comprising at least one of cyclohexanone, cyclopentanone, or an aromatic ketone and an aldehyde and having a molar ratio of ketone to aldehyde of 1:1 to 1:3.
15 to 30% by weight The acid-curing resin used in the wood invention is a resol type phenolic resin, furfuryl alcohol or furan resin, and at least one ketone selected from cyclohexanone, cyclopentanone, and aromatic ketone and an aldehyde. The ketone resin contains a lyketone to aldehyde molar ratio of 1:1 to 1:3.

レゾール型フェノール樹脂としてはフェノール系樹脂、
例えばフェノール、クレゾール、キシレノール、レゾル
シン、アルキルフェノール、フェニルフェノール、ビス
フェノールA等の少なくとも一種と、アルデヒドを縮合
せしめたレゾール型樹脂が挙げられる。
As resol type phenolic resin, phenolic resin,
Examples include resol type resins in which aldehyde is condensed with at least one of phenol, cresol, xylenol, resorcin, alkylphenol, phenylphenol, bisphenol A, and the like.

フラン系樹脂としては尿素、メラミン、尿素/アルデヒ
ド重縮合物、メラミン/アルデヒド重縮合物、アルデヒ
ドの少なくとも一種とフルフリルアルコールを混合また
は共縮合せしめた樹脂が用いられる。
As the furan resin, a resin prepared by mixing or co-condensing at least one of urea, melamine, urea/aldehyde polycondensate, melamine/aldehyde polycondensate, and aldehyde with furfuryl alcohol is used.

ケトン樹脂の成分である芳香族ケトンとしては、アセト
フェノン系ケトン、プロピオフェノン系ケトン、ヘンシ
フエノン系ケトン等が挙げられる。また、アルデヒドと
しては、ホルムアルデヒド(バラホルムアルデヒド及び
トリオキサンのような重合体形態のものを包含する)、
アセトアルデヒド、プロピオンアルデヒド、フチルアル
デヒド、アクロレイン、クロトンアルデヒド、トリグル
アルデヒド、ヘンズアルデヒト、サリチルアルデヒド、
シンナムアルデヒド、グリオキサール等が挙げられるが
、これらに限定されるものではない。アルデヒドとして
は特にホルムアルデヒドが好ましい。
Examples of the aromatic ketone that is a component of the ketone resin include acetophenone ketones, propiophenone ketones, hesiphenone ketones, and the like. Aldehydes also include formaldehyde (including polymeric forms such as paraformaldehyde and trioxane);
Acetaldehyde, propionaldehyde, phthylaldehyde, acrolein, crotonaldehyde, triglyaldehyde, henzaldehyde, salicylaldehyde,
Examples include, but are not limited to, cinnamaldehyde and glyoxal. Formaldehyde is particularly preferred as the aldehyde.

酸硬化性樹脂中のレゾール型フェノール樹脂が20重量
%より少ないと鋳物表面粗度が悪化したり、硬化速度が
遅くなったりする。また35重量%よりも多いとやはり
鋳物表面粗度が悪化したり、可使時間が短くなり使い勝
手が悪くなったりする。また、酸硬化性樹脂中のフルフ
リルアルコール又はフラン樹脂が40重量%よりも少な
いと鋳型強度が低下し、65重量%よりも多いと鋳物表
面粗度が悪化する。更に酸硬化性樹脂中のケトン樹脂が
15重量%よりも少ないと鋳物表面粗度が悪化し、30
重量%よりも多いと鋳型強度が極端に低下する。
If the resol type phenolic resin in the acid-curable resin is less than 20% by weight, the surface roughness of the casting may deteriorate or the curing speed may become slow. If the amount is more than 35% by weight, the surface roughness of the casting may deteriorate, the pot life may be shortened, and the usability may become poor. Furthermore, if the content of furfuryl alcohol or furan resin in the acid-curable resin is less than 40% by weight, the mold strength will decrease, and if it is more than 65% by weight, the surface roughness of the casting will deteriorate. Furthermore, if the ketone resin in the acid-curing resin is less than 15% by weight, the surface roughness of the casting deteriorates,
If the amount is more than 1% by weight, the mold strength will be extremely reduced.

本発明において強酸と弱塩基の塩は粘結剤中の硬化剤と
して作用し、低級脂肪族スルホン酸又は芳香族スルホン
酸のような強酸、具体的には、メチルスルホン酸、エチ
ルスルホン酸、ベンゼンスルホン酸、トルエンスルホン
酸、キシレンスルホン酸、フェノールスルボン酸等の酸
の少なくとも一種とアルミニウム、銅、亜鉛、鉄等の少
なくとも一種との塩を用いるのが好ましい。弱塩基とし
ては、Cu(OH)z、Zn(011)z、Fe (O
H) 2、A I (OH) 3等が挙げられる。
In the present invention, the salt of a strong acid and a weak base acts as a curing agent in the binder, and is used as a hardening agent in the binder, and is used as a hardening agent in the binder. It is preferable to use a salt of at least one of acids such as sulfonic acid, toluenesulfonic acid, xylene sulfonic acid, and phenolsulfonic acid and at least one of aluminum, copper, zinc, iron, and the like. Weak bases include Cu(OH)z, Zn(011)z, Fe(O
H) 2, A I (OH) 3, and the like.

本発明の鋳物砂川粘結剤組成物における酸硬化性樹脂と
強酸と弱塩基の塩の配合比率は、酸硬化性樹脂100重
量部に対して強酸と弱塩基の塩を5〜50重量部、好ま
しくは10〜30重量部である。また、本発明の鋳物砂
川粘結剤組成物は耐火性粒状骨材100重量部に対して
0.5〜4重足部、好ましくは0.8〜2.5重量部使
用される。
The blending ratio of the acid curable resin and the salt of a strong acid and a weak base in the casting Sunagawa binder composition of the present invention is 5 to 50 parts by weight of the salt of a strong acid and a weak base to 100 parts by weight of the acid curable resin. Preferably it is 10 to 30 parts by weight. The casting Sunagawa binder composition of the present invention is used in an amount of 0.5 to 4 parts, preferably 0.8 to 2.5 parts by weight, per 100 parts by weight of the refractory granular aggregate.

本発明の粘結剤組成物は酸硬化性樹脂、強酸と弱塩基の
塩及び必要に応じて用いられる添加剤を別々に耐火性粒
状骨材に混合するのが好ましく、特に強酸と弱塩基の塩
、添加剤、酸硬化性樹脂の順に混合するのが好ましい。
The binder composition of the present invention is preferably prepared by separately mixing an acid-curing resin, a salt of a strong acid and a weak base, and additives used as necessary, into a fire-resistant granular aggregate. It is preferable to mix the salt, additive, and acid-curable resin in this order.

本発明の鋳物砂用粘結剤組成物には必要に応じて、通常
この分野で用いられる変性剤等の添加剤を併用すること
ができる。
If necessary, the binder composition for foundry sand of the present invention may contain additives such as modifiers commonly used in this field.

本発明の鋳物砂川粘結剤組成物に併用できるものとして
は、クマロン・インデン樹脂、石油樹脂、ポリビニルア
ルコール、ポリブタジェン、キシレン樹脂、スチレン樹
脂等のポリマー及びオリゴマー、リグニン、ロジン、エ
ステルガム等の天然物、希釈剤としてヘンゼン、キシレ
ン等の芳香族炭化水素やメタノール、エタノール等の1
価アルコール等が挙げられる。また、鋳型強度を向上さ
せる目的でシランカンブリング剤を加えても差し支えな
い。シランカンプリング剤としては、例えばγ−(2−
アミン)アミノプロピルメチルジメトキシシラン、γ−
アミノプロピルトリメトキシシラン、γ−アミノプロピ
ルトリエトキシシラン、γ−メルカプトプロピルトリメ
トキシシラン、γ−グリシドキシプロピルトリメトキシ
シラン等が挙げられる。
Polymers and oligomers such as coumaron/indene resin, petroleum resin, polyvinyl alcohol, polybutadiene, xylene resin, and styrene resin, natural materials such as lignin, rosin, and ester gum can be used in combination with the foundry Sunagawa binder composition of the present invention. As a diluent, aromatic hydrocarbons such as Hensen and xylene, methanol, ethanol, etc.
Alcohols and the like can be mentioned. Furthermore, a silane cambling agent may be added for the purpose of improving mold strength. Examples of silane camping agents include γ-(2-
amine) aminopropylmethyldimethoxysilane, γ-
Examples include aminopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, γ-mercaptopropyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, and the like.

これらを併用する場合、酸硬化性樹脂と混合して添加し
ても、別に耐火性粒状骨材と混合しても差し支えない。
When these are used together, they may be added together with the acid-curing resin, or may be mixed separately with the fire-resistant granular aggregate.

〔発明の効果〕〔Effect of the invention〕

本発明の鋳物砂川粘結剤組成物によって成型された鋳型
を用いて製造される鋳物の鋳肌の滑らかさは大幅に向上
される。
The smoothness of the casting surface of a casting manufactured using a mold formed using the foundry Sunagawa binder composition of the present invention is greatly improved.

[実施例〕 以下、実施例にて本発明を説明するが、本発明はこれら
の実施例に限定されるものではない。
[Examples] The present invention will be explained below with reference to Examples, but the present invention is not limited to these Examples.

尚、例中の部は何れも重量基準である。Note that all parts in the examples are based on weight.

(1)ケトン樹脂の調製 常法により、シクロへキサノン1モルに対し、ホルムア
ルデヒド2モルをKO)l触媒を用いて反応温度90°
Cで3時間反応させ、軟化点90°Cのケトン樹脂を得
た。
(1) Preparation of ketone resin According to a conventional method, 2 moles of formaldehyde are added to 1 mole of cyclohexanone using a KO)l catalyst at a reaction temperature of 90°C.
C. for 3 hours to obtain a ketone resin with a softening point of 90.degree.

(2)レゾール型フェノール樹脂の調製常法により、フ
ェノール1モルに対し、ホルムアルデヒド1.3モルを
KOH触媒を用いて反応温度80°Cで6時間反応させ
、25°Cにおいて粘度5000cpsのレゾール型フ
ェノール樹脂を得た。
(2) Preparation of resol type phenolic resin By a conventional method, 1 mole of phenol is reacted with 1.3 mole of formaldehyde using a KOH catalyst at a reaction temperature of 80°C for 6 hours, and the resol type has a viscosity of 5000 cps at 25°C. A phenolic resin was obtained.

実施例1〜6及び比較例1〜5 上記で得られたケトン樹脂、レゾール型フェノール樹脂
及びフルフリルアルコールを表−1に示す量混合し、7
0°Cで加熱攪拌して酸硬化性樹脂を得た。
Examples 1 to 6 and Comparative Examples 1 to 5 The ketone resin, resol type phenol resin, and furfuryl alcohol obtained above were mixed in the amounts shown in Table 1, and 7
The mixture was heated and stirred at 0°C to obtain an acid-curable resin.

この酸硬化性樹脂等を用いて鋳型の最終抗折力及び鋳物
表面の粗度を以下の方法で評価した。
Using this acid-curable resin, etc., the final transverse rupture strength of the mold and the roughness of the surface of the casting were evaluated by the following method.

即ち、島根県産浮選珪砂(AFS粒度指数56) 10
0部に対し、酸硬化性樹脂2部、硬化剤としてpトルエ
ンスルホン酸銅塩の水−メタノール溶液(濃度40重量
%)を0.6部及び鋳型強度を向上する目的で花王りエ
ーカー■より市販されている商標名「カオーライトナー
J−20J O,1部を混合し、混練砂組成物を得た。
That is, flotation silica sand from Shimane Prefecture (AFS particle size index 56) 10
0 parts, 2 parts of acid-curing resin, 0.6 parts of a water-methanol solution (concentration 40% by weight) of p-toluenesulfonic acid copper salt as a curing agent, and Kao Riacre ■ for the purpose of improving mold strength. One part of commercially available kaolite toner J-20J O was mixed to obtain a kneaded sand composition.

この混練砂組成物を空気により200”Cに加熱された
金型内に吹き込み、20秒間加熱した後取り出し、22
.4mm X22.4mm X 180mmの試験片を
得、これを1時間放置後、ジョージ・フィッシャー社製
万能強度試験器で最終抗折力を測定した。
This kneaded sand composition was blown into a mold heated to 200"C by air, heated for 20 seconds, and then taken out.
.. A test piece of 4 mm x 22.4 mm x 180 mm was obtained, and after being left for 1 hour, the final transverse rupture strength was measured using a universal strength tester manufactured by George Fisher.

また、混練砂組成物を空気により200°Cに加熱され
た金型内に吹き込み、90秒間加熱した後取り出し、階
段状試験片用鋳型を得、この鋳型内に材質FC−25の
溶湯を注湯温度1420°C1注湯所要時間7秒間で注
湯し、冷却して第1図のような階段状試験片を得た。こ
の階段状試験片の上面6ケ所を触針式表面粗度測定器に
より測定し、その平均値を鋳物表面粗度とした。
In addition, the kneaded sand composition was blown into a mold heated to 200°C by air, heated for 90 seconds, and then taken out to obtain a mold for a step-like test piece, and a molten metal of material FC-25 was poured into this mold. The hot water was poured at a temperature of 1420° C. for a pouring time of 7 seconds, and cooled to obtain a stepped test piece as shown in FIG. Six locations on the upper surface of this stepped test piece were measured using a stylus type surface roughness measuring device, and the average value was taken as the casting surface roughness.

以上の結果を表−1に示す。The above results are shown in Table-1.

table

【図面の簡単な説明】[Brief explanation of drawings]

第1図(a)は実施例で用いた階段状試験片の平面図、
第1図(b)はその側面図である。尚、図中寸法単位は
mmである。
FIG. 1(a) is a plan view of the stepped test piece used in the example;
FIG. 1(b) is a side view thereof. Note that the dimensional unit in the figure is mm.

Claims (1)

【特許請求の範囲】 1 酸硬化性樹脂、及び強酸と弱塩基の塩からなり、耐
火性粒状骨材に混練してこれを加熱硬化させることによ
り鋳型を成型する際に用いられる鋳物砂用粘結剤組成物
であって、前記酸硬化性樹脂が下記の組成を有すること
を特徴とする鋳物砂用粘結剤組成物。 (a)レゾール型フェノール樹脂20〜35重量% (b)フルフリルアルコール又はフラン樹脂40〜65
重量% (c)シクロヘキサノン、シクロペンタノン及び芳香族
ケトンから選ばれた少なくとも1種のケトンとアルデヒ
ドからなりケトン対アルデヒドのモル比が1:1〜1:
3のケトン樹脂15〜30重量% 2 強酸と弱塩基の塩が、低級脂肪族スルホン酸又は芳
香族スルホン酸の少なくとも1種と弱塩基の塩である請
求項1記載の鋳物砂用粘結剤組成物。 3 低級脂肪族スルホン酸又は芳香族スルホン酸と弱塩
基の塩が、ベンゼンスルホン酸、フェノールスルホン酸
、トルエンスルホン酸、キシレンスルホン酸及び低級ア
ルキルスルホン酸からなる群より選ばれる少なくとも1
種とアルミニウム、銅、亜鉛及び鉄からなる群より選ば
れる少なくとも1種との塩である請求項2記載の鋳物砂
用粘結組成物。
[Scope of Claims] 1 A clay for foundry sand that is made of an acid-curable resin and a salt of a strong acid and a weak base, and is used when molding a mold by kneading it into refractory granular aggregate and curing it by heating. A binder composition for foundry sand, characterized in that the acid-curable resin has the following composition. (a) Resol type phenolic resin 20-35% by weight (b) Furfuryl alcohol or furan resin 40-65%
Weight% (c) Comprising at least one ketone selected from cyclohexanone, cyclopentanone, and aromatic ketones and an aldehyde, and the molar ratio of ketone to aldehyde is 1:1 to 1:
2. The binder for foundry sand according to claim 1, wherein the salt of a strong acid and a weak base is a salt of a weak base and at least one of lower aliphatic sulfonic acids or aromatic sulfonic acids. Composition. 3. At least one salt of a lower aliphatic sulfonic acid or an aromatic sulfonic acid and a weak base is selected from the group consisting of benzenesulfonic acid, phenolsulfonic acid, toluenesulfonic acid, xylene sulfonic acid, and lower alkylsulfonic acid.
The caking composition for foundry sand according to claim 2, which is a salt of a seed and at least one member selected from the group consisting of aluminum, copper, zinc, and iron.
JP24072590A 1990-09-11 1990-09-11 Binder composition for foundry sand Expired - Fee Related JP2831826B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP24072590A JP2831826B2 (en) 1990-09-11 1990-09-11 Binder composition for foundry sand

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP24072590A JP2831826B2 (en) 1990-09-11 1990-09-11 Binder composition for foundry sand

Publications (2)

Publication Number Publication Date
JPH04123836A true JPH04123836A (en) 1992-04-23
JP2831826B2 JP2831826B2 (en) 1998-12-02

Family

ID=17063776

Family Applications (1)

Application Number Title Priority Date Filing Date
JP24072590A Expired - Fee Related JP2831826B2 (en) 1990-09-11 1990-09-11 Binder composition for foundry sand

Country Status (1)

Country Link
JP (1) JP2831826B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101927319A (en) * 2010-04-29 2010-12-29 苏州市兴业铸造材料有限公司 Adhesive applicable for manufacturing casting mold and use thereof
CN113560485A (en) * 2021-06-23 2021-10-29 宁波日月精华精密制造有限公司 Copper salt catalyzed resin sand and sand shooting forming process thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101927319A (en) * 2010-04-29 2010-12-29 苏州市兴业铸造材料有限公司 Adhesive applicable for manufacturing casting mold and use thereof
CN113560485A (en) * 2021-06-23 2021-10-29 宁波日月精华精密制造有限公司 Copper salt catalyzed resin sand and sand shooting forming process thereof

Also Published As

Publication number Publication date
JP2831826B2 (en) 1998-12-02

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