JPS6240949A - Resin composition for coated sand - Google Patents

Resin composition for coated sand

Info

Publication number
JPS6240949A
JPS6240949A JP18090385A JP18090385A JPS6240949A JP S6240949 A JPS6240949 A JP S6240949A JP 18090385 A JP18090385 A JP 18090385A JP 18090385 A JP18090385 A JP 18090385A JP S6240949 A JPS6240949 A JP S6240949A
Authority
JP
Japan
Prior art keywords
resin
sand
coated sand
casting
furan
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
JP18090385A
Other languages
Japanese (ja)
Other versions
JPH0647143B2 (en
Inventor
Shunsaku Tachibana
俊作 橘
Mitsuo Yokoi
横井 満雄
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.)
KOBE RIKAGAKU KOGYO KK
Original Assignee
KOBE RIKAGAKU KOGYO KK
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 KOBE RIKAGAKU KOGYO KK filed Critical KOBE RIKAGAKU KOGYO KK
Priority to JP60180903A priority Critical patent/JPH0647143B2/en
Publication of JPS6240949A publication Critical patent/JPS6240949A/en
Publication of JPH0647143B2 publication Critical patent/JPH0647143B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Mold Materials And Core Materials (AREA)
  • Polyethers (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

PURPOSE:To obtain a resin compsn. for coated sand for a shell mold method which has a good collapsing property of a core during low-temp. casting and obviates the generation of casting defects arising from the generation of gaseous nitrogen in a casting stage by using a furan resin having specific structure as an essential component. CONSTITUTION:The resin compsn. for coated sand for a casting essentially consisting of the furan resin including >=2, more preferably 2-4 furan rings in one molecule adequately contains 30-100wt% above-mentioned furan resin. The above-mentioned furan resin is obtd. by polymerizing furfuryl alcohol alone or furfuryl alcohol and aldehyde in the presence of an acidic catalyst such as phosphoric acid or xylene sulfonic acid. The above-mentioned resin compsn. is thrown into the heated molding sand at about 0.8-8wt% by 100pts.wt. molding sand and the mixture is thoroughly agitated by a mixer to uniformly stick the resin compsn. on the surface of the molding sand. The coated sand is thus obtd.

Description

【発明の詳細な説明】 産業上の利用分野 本発明はシェルモールド法に用いられるコーテツドサン
ド用樹脂組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a resin composition for coated sand used in shell molding.

従来技術 従来、一般にシェルモールド法に用いるコーテツドサン
ド用樹脂組成物としては、フェノール類とホルムアルデ
ヒド類を触媒の存在下で反応したノボラック型フェノー
ル樹脂と硬化剤としてのへギサメヂレンテトラミンから
成る組成物が知られ、この混合物を鋳物用砂粒と混合し
てシェルモールド用レジンコーテツドサンドが作られて
いる。
Conventional technology Conventionally, resin compositions for coated sand generally used in the shell molding method are composed of a novolac type phenolic resin obtained by reacting phenols and formaldehydes in the presence of a catalyst, and hegisamidetetramine as a curing agent. Compositions are known and this mixture is mixed with foundry sand grains to make resin-coated sand for shell molds.

しかしながら、従来のフェノール樹脂を用いたコーテツ
ドサンドより作られたシェル鋳型(J1造型時の焼成中
にヘキサメチレンテトラミンが分解してアンモニア臭を
発生し、作業環境を悪くする欠点がある。また注湯時に
おいてもヘキサメチレンテトラミンの熱分解によって発
生する窒素ガスが鋳物に悪影響を及ぼすという欠点もあ
る。
However, shell molds made from coated sand using conventional phenolic resin have the disadvantage that hexamethylenetetramine decomposes during firing during J1 molding and generates an ammonia odor, which worsens the working environment. There is also the drawback that nitrogen gas generated by thermal decomposition of hexamethylenetetramine has an adverse effect on castings even when hot water is used.

さらに、鉄のごとき高融点金属を鋳造する際フェノール
樹脂を用いたコーテッドザンドシエル鋳型を用いると、
鋳型が高温にさらされ、フェノール樹脂が熱分解し、鋳
型は崩壊する。しかしながら、アルミニウムのような低
融点の軽金属を注湯した場合、シェル鋳型の内部温度が
300〜500°Cという低温にとどまる。このため、
フェノール樹脂の熱分解が不十分となり、崩壊性が悪く
、中子を鋳物より取り出すのが著しく困難となる場合が
ある。このため、シェル中子を取り出すには、鋳物を焼
成炉でいわゆる砂焼きと称する長時間加熱をして中子を
崩壊させろ方法がとられている。このことは、エネルギ
ーの無駄と生産性の低下につながり、改良が望まれてい
る。
Furthermore, when casting high-melting point metals such as iron, using coated sandshell molds made of phenolic resin,
The mold is exposed to high temperatures, the phenolic resin thermally decomposes, and the mold collapses. However, when a light metal with a low melting point such as aluminum is poured, the internal temperature of the shell mold remains at a low temperature of 300 to 500°C. For this reason,
Thermal decomposition of the phenolic resin may be insufficient, resulting in poor collapsibility, and it may be extremely difficult to remove the core from the casting. For this reason, in order to remove the shell core, a method is used in which the casting is heated in a kiln for a long period of time in a so-called sand firing process to cause the core to collapse. This leads to wasted energy and reduced productivity, and improvements are desired.

一方、フルフラールやフルフリルアルコールを主成分と
し、これに尿素、ホルムアルデヒド、フェノールなどを
配合し、酸触媒を用いて重合させて得られろ液状の初期
硬化物(通常、フラン樹脂と称されている)が、ポット
ボックス用等の鋳物砂川粘結剤として用いられている。
On the other hand, a filtrate-like initial cured product (usually called furan resin) is obtained by polymerizing furfural or furfuryl alcohol as a main component with urea, formaldehyde, phenol, etc. using an acid catalyst. ) is used as a foundry Sunagawa binder for pot boxes, etc.

しかし、これらのフルフリルアルコールを主成分とする
樹脂は、フルフリルアルコールがモノマーかフラン環を
分子中に1つしか含まない低分子物質であるため、常温
で液体であり、鋳物用砂粒と混合しても、ウェットな状
態にとどまり、シェルモールド用のさらさらとした流動
性のよいコーテツドサンドを得ることはできない。
However, these resins whose main component is furfuryl alcohol are liquid at room temperature because furfuryl alcohol is a monomer or a low-molecular substance containing only one furan ring in the molecule, and cannot be mixed with foundry sand grains. However, the coated sand remains wet and smooth and fluid coated sand for shell molding cannot be obtained.

特公昭40−28443号公報に(jl シェルモール
ド用粘結剤にフルフリルアルコール変性尿素ホルムアル
デヒド樹脂の初期縮合物を用いろ提案がされている。こ
の技術(」、従来のフラン樹脂が低粘度でシェルモール
ド用コーティング砂を得るには不適当であったため、そ
の粘度をあげかつ速硬性とするためウレイドとしたもの
であり、低温鋳造時における中子の崩壊性を向」−させ
る等の技術は全く示唆されていない。
Japanese Patent Publication No. 40-28443 proposes the use of an initial condensate of furfuryl alcohol-modified urea formaldehyde resin as a binder for shell molds. Since it was unsuitable for obtaining coating sand for shell molds, it was made with ureid to increase its viscosity and make it harden quickly. Not suggested at all.

発明が解決しようとする問題点 本発明は従来シェルモールド用コーテヅドザンド用粘結
剤として用いられていた、フェノール系樹脂の欠点であ
るアルミニウム鋳型のごとき低温鋳造時における中子の
分解不良や、硬化剤(ヘキザメヂレンテトラミン)に起
因するアンモニウム臭ならびに熱分解によって生ずる窒
素ガスにもとづく鋳物欠陥等を生じないコーテツドサン
ド用樹脂組成物を提供する。
Problems to be Solved by the Invention The present invention addresses the drawbacks of phenolic resins conventionally used as binders for coated sand for shell molds, such as poor decomposition of cores during low-temperature casting such as aluminum molds, and hardening agents. To provide a resin composition for coated sand that does not cause casting defects due to ammonium odor caused by (hexamedylenetetramine) and nitrogen gas generated by thermal decomposition.

問題点を解決するための手段 −3〜 本発明は1分子中にフラン環を2個以」二含むフラン樹
脂を主成分とする鋳物用コーテツドサンド用樹脂組成物
に関する。
Means for Solving the Problems - 3~ The present invention relates to a resin composition for coated sand for foundries, the main component of which is a furan resin containing two or more furan rings in one molecule.

本発明に用いるフラン樹脂はフルフリルアルコールまた
はフルフリルアルコールとアルデヒド類とを酸触媒の存
在下に反応させて得られる重合度2〜IO1特に2〜4
の樹脂である。
The furan resin used in the present invention is obtained by reacting furfuryl alcohol or furfuryl alcohol with an aldehyde in the presence of an acid catalyst and has a polymerization degree of 2 to IO1, particularly 2 to 4.
It is a resin.

フルフリルアルコール単独あるいはフルフリルアルコー
ルとアルデヒド類を反応させるための酸性触媒としては
、リン酸、硫酸、塩酸等の無機酸水溶液、またキシレン
スルポン酸、トルエンスルポン酸、ベンゼンスルホン酸
、蓚酸、乳酸等の有機酸を用いることもできる。反応後
、反応液を中和して未反応フルフリルアルコール、未反
応アルデヒド類、縮合水を除去するため減圧下で脱水操
作を行い、1分子中にフラン環を2個以上含むように重
合反応を進める。反応物を水で洗浄してから脱水操作を
してもよい。
Acidic catalysts for reacting furfuryl alcohol alone or with furfuryl alcohol and aldehydes include inorganic acid aqueous solutions such as phosphoric acid, sulfuric acid, and hydrochloric acid, as well as xylene sulfonic acid, toluene sulfonic acid, benzenesulfonic acid, oxalic acid, Organic acids such as lactic acid can also be used. After the reaction, dehydration is performed under reduced pressure to neutralize the reaction solution and remove unreacted furfuryl alcohol, unreacted aldehydes, and condensed water, and the polymerization reaction is performed so that one molecule contains two or more furan rings. proceed. The reaction product may be washed with water and then dehydrated.

また本発明において、アルデヒド類としてはホルムアル
デヒド、アセトアルデヒド、グリオキザ一部等を使用す
ることができる。本発明は必らずしもアルデヒド類を用
いなくても良いが、用いない場合に比べ、一般に樹脂の
反応を速く進めることができる。
In the present invention, formaldehyde, acetaldehyde, a portion of glyoxa, etc. can be used as aldehydes. Although the present invention does not necessarily require the use of aldehydes, the reaction of the resin can generally proceed more quickly than when aldehydes are not used.

本発明の樹脂成分として、フェノール類、例えばフェノ
ール、クレゾール、ビスフェノール等を一部配合しても
よいが、これらを配合すると一般に樹脂粘度は低下する
As the resin component of the present invention, a portion of phenols such as phenol, cresol, bisphenol, etc. may be blended, but when these are blended, the resin viscosity generally decreases.

本発明樹脂組成物は一般に常温で固体であるが、これを
微粉砕するか、あるいは塊状のまま加熱した鋳物砂中に
投入し、ミキサーで十分攪拌することにより、鋳物砂表
面に均一に付着させる。
The resin composition of the present invention is generally solid at room temperature, but it can be made to adhere uniformly to the surface of the foundry sand by pulverizing it or putting it into heated foundry sand in the form of a lump, and thoroughly stirring it with a mixer. .

鋳物砂100重量部に対し、本発明樹脂組成物0.8〜
8重量部、特に1〜5重量部を配合する。
0.8 to 100 parts by weight of the resin composition of the present invention per 100 parts by weight of foundry sand
8 parts by weight, especially 1 to 5 parts by weight.

本発明樹脂組成物には必要により、カップリング剤(例
え、ばジメトキシシラン)、滑剤(スlテアリン酸カル
シウム)等を配合してもよい。
The resin composition of the present invention may contain a coupling agent (for example, dimethoxysilane), a lubricant (calcium stearate), etc., if necessary.

さらに本発明によるコーテツドサンド用樹脂組成物を用
いて、鋳物用砂粒と混合してコーテツドサンドを作製す
る方法において、滑剤として脂肪酸アマイド類、脂肪酸
カルシウム類、ワックス類を添加して流動性を改良して
もよい。これらはあらかじめ樹脂組成物に内添して用い
てもよい。また、強度改良剤としてシラン化合物を樹脂
組成物に内添するか、あるい(Jコ−テッドサンド作製
時に添加してもよい。
Furthermore, in a method of producing coated sand by mixing the resin composition for coated sand according to the present invention with foundry sand grains, fatty acid amides, fatty acid calcium, and waxes are added as lubricants to improve fluidity. May be improved. These may be used by being added internally to the resin composition in advance. In addition, a silane compound may be added internally to the resin composition as a strength improver, or may be added at the time of producing the J-coated sand.

本発明をさらに効果的にならしめろ方法として、コーテ
ツドサンドを作製する場合、蓚酸、ザリチル酸、マレイ
ン酸、ホウ酸、パラトルエンスルポン酸等の常温で固形
の酸を樹脂組成物に対して05〜10重重%添加するこ
とにより、コーテツドサンドの焼成温度を低くしたり、
焼成時間を短くすることができる。
As a more effective conditioning method of the present invention, when producing coated sand, an acid that is solid at room temperature such as oxalic acid, salicylic acid, maleic acid, boric acid, paratoluene sulfonic acid, etc. is added to the resin composition. By adding 05 to 10% by weight, the firing temperature of coated sand can be lowered,
Firing time can be shortened.

以下、実施例を挙げて本発明を説明する。The present invention will be explained below with reference to Examples.

夾施%j+ 四ツ目フラスコにフルフリルアルコール300g、水1
50g、反応触媒として20%りん酸4gを添加して1
)T(2,0とした。徐々に温度をあげて、反応温度9
5℃で9時間反応させた。
Concentration %j+ 300g furfuryl alcohol, 1 water in a four-eye flask
50g, 4g of 20% phosphoric acid was added as a reaction catalyst, and 1
)T(2,0. Gradually raise the temperature until the reaction temperature is 9.
The reaction was carried out at 5°C for 9 hours.

反応後、20%水酸化ナトリウム水溶液により反応液を
中和して1)H6,5とした。その後、減圧度−600
mmHgで樹脂温度り月05℃になるまで脱水した。
After the reaction, the reaction solution was neutralized with a 20% aqueous sodium hydroxide solution to obtain 1) H6.5. After that, the degree of decompression is -600
The resin was dehydrated at mmHg until the resin temperature reached 05°C.

次に、200°Cに加熱したフラタリーザンド4kgを
スピードミギザーに投入して、」二記の樹脂組成物12
0gを添加し、混合物がブロッキングを始めた時にステ
アリン酸カルシウム4gを加えて冷却し、コーテツドサ
ンドを作製した。流動性のあるコーテツドサンドを得た
。このコーテツドサンドの抗折力を測定した。結果を表
1に示す。
Next, 4 kg of Flatarisand heated to 200°C was put into the Speed Migizer, and the resin composition 12 of "2.
When the mixture started blocking, 4 g of calcium stearate was added and cooled to prepare coated sand. A fluid coated sand was obtained. The transverse rupture strength of this coated sand was measured. The results are shown in Table 1.

また、このコーテツドサンドを用いたシェル鋳型でアル
ミニウム鋳物AC−40を鋳込んだところ、フェノール
樹脂を用いたシェル鋳型に比べ、崩壊性が非常に良好で
あった。
Furthermore, when an aluminum casting AC-40 was cast using a shell mold using this coated sand, the collapsibility was very good compared to a shell mold using a phenol resin.

実施例2 実施例1の合成法で37%ホルマリン80gを添加する
他は実施例1を繰返した。このコーテツドサンドを用い
て抗折力を測定したところ表=1に示す結果が得られた
Example 2 Example 1 was repeated using the synthesis method of Example 1 except that 80 g of 37% formalin was added. When the transverse rupture strength was measured using this coated sand, the results shown in Table 1 were obtained.

また、このコーテツドサンドを用いたシェル鋳型でアル
ミニウム鋳物AC1Cを鋳込んだところ、フェノール樹
脂を用いたシェル鋳型に比べ崩壊性が非常に良好であっ
た。
Furthermore, when an aluminum casting AC1C was cast using a shell mold using this coated sand, the collapsibility was very good compared to a shell mold using a phenol resin.

実施週4一 実施例2において合成した樹脂にジメトキシノランを樹
脂に対し0.5重量%添加した。
Week 4 - Dimethoxynolan was added to the resin synthesized in Example 2 in an amount of 0.5% by weight based on the resin.

実施例1と同様にして、」二記の樹脂を使用してコーテ
ツドサンドを作製した。
Coated sand was prepared in the same manner as in Example 1 using the resin described in "2".

該コーテツドサンドを用いて得られた砂型の試験結果を
表−Iに示す。
Table I shows the test results of sand molds obtained using the coated sand.

実施例4 実施例2において合成した樹脂にメヂレンビスステアリ
ン酸アミドを対樹脂3%添加した。
Example 4 To the resin synthesized in Example 2, methylene bisstearic acid amide was added in an amount of 3% based on the resin.

実施例1と同方法により、上記の樹脂を使用してコーテ
ツドサンドを作製した。
Coated sand was produced using the above resin in the same manner as in Example 1.

」二記コーテツドサンドから得られた砂型の試験結果を
表−1に示す。
Table 1 shows the test results of sand molds obtained from the coated sand mentioned above.

実施例5 実施例1で作製したフランコーテツドサンドに硬化促進
剤として固体酸性物質(ザリチル酸)を鋳物砂に対し0
.1重量%添加した。
Example 5 A solid acidic substance (salicylic acid) was added as a hardening accelerator to the Francoated sand produced in Example 1 to foundry sand.
.. 1% by weight was added.

表−1に実施例1〜5において作製したフランコーテツ
ドサンドを用いた砂型の試験結果を示す。
Table 1 shows the test results of sand molds using Franco-coated sand produced in Examples 1 to 5.

表−1 [単  位:  Kg/cm’、金型保持時間60秒]
[曲げ強さ:  JIS  K6910により測定]発
明の効果 本発明コーテツドサンド用樹脂組成物を被覆した鋳物砂
をアルミニウム等の低温鋳造(内部温度300〜500
℃)用中子に用いると、鋳造後、中子は容易に崩壊して
簡単に取り除くことができる。従って、従来のフェノー
ル系樹脂のごとき高温での砂焼を必要とせず、鋳造工程
を簡略化し、時間を短縮できる。また、ヘキザメチレン
テトラミンのごとき硬化剤を必要としないため、鋳造工
程での窒素ガスの発生がなく、従って、窒素ガスにもと
づく鋳造欠陥を生じない。
Table-1 [Unit: Kg/cm', mold holding time 60 seconds]
[Bending strength: Measured according to JIS K6910] Effects of the invention The foundry sand coated with the resin composition for coated sand of the present invention is used for low-temperature casting of aluminum etc. (internal temperature 300-500
When used in cores for 300 °C), the cores easily disintegrate and can be easily removed after casting. Therefore, unlike conventional phenolic resins, high-temperature sand firing is not required, which simplifies the casting process and shortens the time. Furthermore, since a hardening agent such as hexamethylenetetramine is not required, no nitrogen gas is generated during the casting process, and therefore no casting defects due to nitrogen gas occur.

Claims (1)

【特許請求の範囲】 1、1分子中にフラン環を2個以上含むフラン樹脂を主
成分とする鋳物用コーテッドサンド用樹脂組成物。 2、フラン樹脂がフルフリルアルコールの単独重合体で
ある第1項記載の樹脂組成物。 3、フラン樹脂がフルフリルアルコールとアルデヒドと
の重合体である第1項記載の樹脂組成物。 4、1分子中にフラン環を2〜4個有する第1項記載の
樹脂組成物。 5、フラン樹脂を30〜100重量%含有する第1項記
載の樹脂組成物。
[Claims] 1. A resin composition for coated sand for foundries, the main component of which is a furan resin containing two or more furan rings in each molecule. 2. The resin composition according to item 1, wherein the furan resin is a homopolymer of furfuryl alcohol. 3. The resin composition according to item 1, wherein the furan resin is a polymer of furfuryl alcohol and aldehyde. 4. The resin composition according to item 1, having 2 to 4 furan rings in one molecule. 5. The resin composition according to item 1, containing 30 to 100% by weight of furan resin.
JP60180903A 1985-08-16 1985-08-16 Resin composition for coated sand Expired - Lifetime JPH0647143B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60180903A JPH0647143B2 (en) 1985-08-16 1985-08-16 Resin composition for coated sand

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60180903A JPH0647143B2 (en) 1985-08-16 1985-08-16 Resin composition for coated sand

Publications (2)

Publication Number Publication Date
JPS6240949A true JPS6240949A (en) 1987-02-21
JPH0647143B2 JPH0647143B2 (en) 1994-06-22

Family

ID=16091320

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JPH0647143B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011089008A (en) * 2009-10-22 2011-05-06 Sekisui Chem Co Ltd Method for producing curable resin composition
WO2012124491A1 (en) * 2011-03-17 2012-09-20 旭有機材工業株式会社 Method for producing spherical furfuryl alcohol resin particles, spherical furfuryl alcohol resin particles produced thereby, spherical carbon particles and spherical activated carbon particles
CN103600024A (en) * 2013-11-28 2014-02-26 吴江市液铸液压件铸造有限公司 Precoated sand mixing process
CN105108033A (en) * 2015-08-11 2015-12-02 安徽省胜峰机械有限公司 High-breathability shell powder-contained modified furan resin sand for steel castings and preparation method thereof

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Cited By (7)

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JP2011089008A (en) * 2009-10-22 2011-05-06 Sekisui Chem Co Ltd Method for producing curable resin composition
WO2012124491A1 (en) * 2011-03-17 2012-09-20 旭有機材工業株式会社 Method for producing spherical furfuryl alcohol resin particles, spherical furfuryl alcohol resin particles produced thereby, spherical carbon particles and spherical activated carbon particles
JP2012193299A (en) * 2011-03-17 2012-10-11 Asahi Organic Chemicals Industry Co Ltd Method for producing spherical furfuryl alcohol resin particle, spherical furfuryl alcohol resin particle produced thereby, spherical carbon particle, and spherical activated carbon particle
CN103443164A (en) * 2011-03-17 2013-12-11 旭有机材工业株式会社 Method for producing spherical furfuryl alcohol resin particles, spherical furfuryl alcohol resin particles produced thereby, spherical carbon particles and spherical activated carbon particles
US9040656B2 (en) 2011-03-17 2015-05-26 Asahi Organic Chemicals Industry Co., Ltd. Process for producing spherical particles of furfuryl alcohol resin, spherical particles of furfuryl alcohol resin produced by the process, spherical carbon particles and spherical activated carbon particles
CN103600024A (en) * 2013-11-28 2014-02-26 吴江市液铸液压件铸造有限公司 Precoated sand mixing process
CN105108033A (en) * 2015-08-11 2015-12-02 安徽省胜峰机械有限公司 High-breathability shell powder-contained modified furan resin sand for steel castings and preparation method thereof

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