JPH0318531B2 - - Google Patents
Info
- Publication number
- JPH0318531B2 JPH0318531B2 JP62325456A JP32545687A JPH0318531B2 JP H0318531 B2 JPH0318531 B2 JP H0318531B2 JP 62325456 A JP62325456 A JP 62325456A JP 32545687 A JP32545687 A JP 32545687A JP H0318531 B2 JPH0318531 B2 JP H0318531B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- mold
- parts
- sand
- binder composition
- 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.)
- Expired - Lifetime
Links
- 229920005989 resin Polymers 0.000 claims description 16
- 239000011347 resin Substances 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 15
- 239000011230 binding agent Substances 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 10
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 10
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims description 8
- 150000002895 organic esters Chemical class 0.000 claims description 8
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 6
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 4
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 claims description 4
- 239000011134 resol-type phenolic resin Substances 0.000 claims description 4
- GGNQRNBDZQJCCN-UHFFFAOYSA-N benzene-1,2,4-triol Chemical compound OC1=CC=C(O)C(O)=C1 GGNQRNBDZQJCCN-UHFFFAOYSA-N 0.000 claims description 2
- 229940079877 pyrogallol Drugs 0.000 claims description 2
- 239000003513 alkali Substances 0.000 claims 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 claims 1
- 239000007809 chemical reaction catalyst Substances 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 229910000000 metal hydroxide Inorganic materials 0.000 claims 1
- 150000004706 metal oxides Chemical class 0.000 claims 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 21
- 239000004576 sand Substances 0.000 description 17
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 15
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
- 239000005011 phenolic resin Substances 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
- 229920003987 resole Polymers 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- 238000005266 casting Methods 0.000 description 5
- 229960001755 resorcinol Drugs 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 4
- 150000002989 phenols Chemical class 0.000 description 4
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229920001568 phenolic resin Polymers 0.000 description 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920001228 polyisocyanate Polymers 0.000 description 2
- 239000005056 polyisocyanate Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 2
- JIRHAGAOHOYLNO-UHFFFAOYSA-N (3-cyclopentyloxy-4-methoxyphenyl)methanol Chemical compound COC1=CC=C(CO)C=C1OC1CCCC1 JIRHAGAOHOYLNO-UHFFFAOYSA-N 0.000 description 1
- JTXMVXSTHSMVQF-UHFFFAOYSA-N 2-acetyloxyethyl acetate Chemical compound CC(=O)OCCOC(C)=O JTXMVXSTHSMVQF-UHFFFAOYSA-N 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229930188620 butyrolactone Natural products 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
- 239000007849 furan resin Substances 0.000 description 1
- 150000002240 furans Chemical class 0.000 description 1
- 235000013773 glyceryl triacetate Nutrition 0.000 description 1
- 239000001087 glyceryl triacetate Substances 0.000 description 1
- 229960004337 hydroquinone Drugs 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052609 olivine Inorganic materials 0.000 description 1
- 239000010450 olivine Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
Description
〔産業上の利用分野〕
本発明は、常温硬化型鋳型造形法に用いる鋳型
強度の優れた粘結剤組成物に関する。
〔従来技術〕
常温硬化型鋳型造形法には、有機系又は無機系
の各種粘結剤を用いる方法がある。
無機系粘結剤を用いた鋳型は鋳込み後の砂の崩
壊性が悪く、かつ砂の回収が困難である。
有機系粘結剤を用いる造形法として尿素変性フ
ラン樹脂又はレゾール型フエノール樹脂をキシレ
ンスルホン酸等の強酸性物質を硬化剤として使用
する方法がある。この方法は鋳込み後の鋳型の崩
壊性は良好であるが、硬化剤中のスルホン酸基が
鋳込み時に分解し、亜硫酸ガス等を発生するため
作業環境を悪化させる欠点がある。
有機系粘結剤を用いる別の方法として、ベンジ
リツクエーテル型フエノール樹脂とポリイソシア
ネート液とをアミン類により硬化させる造形法は
造形時間が短く、作業性も良いが、ポリイソシア
ネートに起因する窒素分が鋳込み時に窒素ガスと
なり、鋳物にピンホールを発生させやすい。
また、窒素を含まない方法として、レゾール型
フエノール樹脂と有機エステルを粘結剤とした鋳
型造形法が特公昭61−43132及び特公昭61−37032
に示されている。しかし、この方法では、得られ
た鋳型は強度が極めて低いため、粘結剤を多く必
要とし、用途が制限されるという問題がある。
〔発明の目的〕
本発明者は有機エステルを硬化触媒として用い
る鋳型造形法用フエノール樹脂について種々研究
した結果、多価フエノールを用いて得られるレゾ
ール型多価フエノール樹脂が強度の優れた鋳型を
得るのに特に有効との知見を得た。
更に、この知見に基づいて検討を進め、本発明
を完成するに至つたものである。
〔発明の構成〕
本発明は、樹脂と有機エステルとを使用する常
温硬化型鋳型造形法に用いる粘結剤組成物におい
て、前記樹脂がレゾール型多価フエノール樹脂で
あることを特徴とする鋳型用粘結剤組成物、であ
る。
ここでレゾール型多価フエノール樹脂とは、多
価フエノールとホルムアルデヒドとをアルカリ性
触媒により反応して得られる液状樹脂である。
多価フエノール類とは、2個以上の水酸基を有
するフエノールであり、カテコール、レゾルシ
ン、ハイドロキノン、ピロガロール、オキシハイ
ドロキノン、フロログリシン等であり、これらを
単独又は混合して使用することができる。
ホルムアルデヒドは通常ホルマリンの形で用い
られる。ホルムアルデヒドの多価フエノール類に
対する使用比率はモル比で0.5〜3.0である。
触媒として使用されるアルカリ性物質は通常水
酸化カリウム、水酸化ナトリウム、水酸化リチウ
ム、水酸化カルシウム等のアルカリ金属又はアル
カリ土類金属の水酸化物又は酸化物であり、多価
フエノールに対してモル比で0.2〜2.0の割合で使
用される。
また、γ−グリシドオキシ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
ン等のシランカツプリング剤を樹脂に対して0.2
〜3.0重量%添加混合することにより更に高強度
の鋳型が得られる。
本発明のレゾール型多価フエノール樹脂は単独
で、又は通常のレゾール型フエノール樹脂と併用
して使用することができる。
硬化触媒として用いる有機エステルは、蟻酸メ
チル、蟻酸エチル、蟻酸プロピル、ブチロラクト
ン、エチレングリコールジアセテート、トリアセ
チンなどである。有機エステルは、砂と樹脂との
混合時に添加する方法、あるいは砂と樹脂との混
合物にガス化して添加する方法のいずれも可能で
ある。
有機エステルのフエノール樹脂に対する割合は
重量比で0.1〜0.5が適当である。0.1未満ではフエ
ノール樹脂の硬化が不十分となり、0.5を越えて
も硬化の程度は大きくならない。
鋳物砂は、珪砂、ジルコン砂、クロマイト砂、
オリビン砂及びこれらの再生砂などが使用でき
る。樹脂及び有機エステルの鋳物砂に対する使用
量は重量比で各々0.005〜0.04及び0.001〜0.02が
適当である。
〔発明の効果〕
本発明に従うと、高強度でかつガス欠陥の少な
い鋳型が得られるので、工業的な鋳型造形方法と
して極めて好適である。
[実施例]
以下、本発明を実施例により説明する。本発明
は実施例によつて限定されるものではない。ま
た、実施例、比較例、応用例で示されている
「部」および「%」はすべて重量部及び重量%で
ある。
実施例 1
冷却器及び攪拌器の付いた反応容器にレゾルシ
ン1000部及び37%ホルマリン1474部を仕込み60℃
に加熱した。
次いで、50%水酸化カリウム水溶液610部を30
分かけて添加した。反応液の温度を75〜80℃に高
め、樹脂粘度が2.5〜3.0ポイズ/25℃になるまで
反応を行つた。
所定の粘度に到達した後、速やかに30℃以下に
冷却して、γ−アミノプロピルトリエトキシシラ
ン30部を添加混合し、粘度3.0ポイズ/25℃のレ
ゾール型レゾルシン樹脂3030部を得た。
実施例 2
実施例1において、レゾルシン500部及びカテ
コール500部を用いた以外は実施例1と同様に反
応を行い、粘度3.2ポイズ/25℃のレゾール型レ
ゾルシン・カテコール樹脂3040部を得た。
比較例
冷却器及び攪拌器の付いた反応容器にフエノー
ル1000部及び37%ホルマリン1725部を仕込み60℃
に加熱した。
次いで、50%水酸化カリウム水溶液715部を30
分かけて添加した。反応液の温度を75〜80℃に高
め、樹脂粘度が0.8〜1.2ポイズ/25℃になるまで
反応を行つた後、70Torrの減圧下で250部の水を
除去した。
その後、速やかに30℃以下に冷却して、γ−ア
ミノプロピルトリエトキシシラン32部を添加混合
し、粘度3.0ポイズ/25℃のレゾール型フエノー
ル樹脂3200部を得た。
応用例
品川式卓上型混合機にフリーマントル珪砂3000
部及びトリアセチン15部を投入し、30秒間混合
後、実施例1、実施例2又は比較例の樹脂を各々
60部添加し、60秒間混合して配合砂を調製した。
混合直後の配合砂を径50mm、高さ50mmの造形部
を有する木型に入れてプラスチツクハンマーで3
回たたいた後、余分の砂を除去して造形された配
合砂上面を平滑にした。
木型内で配合砂の硬化後、鋳型を取り出し圧縮
強度を測定した。
その結果を第1表に示す。
[Industrial Field of Application] The present invention relates to a binder composition that has excellent mold strength and is used in a cold-curing mold forming method. [Prior Art] Room temperature curing mold forming methods include methods using various organic or inorganic binders. A mold using an inorganic binder has poor sand disintegration properties after casting, and it is difficult to recover the sand. As a modeling method using an organic binder, there is a method in which a urea-modified furan resin or a resol type phenol resin is used with a strong acidic substance such as xylene sulfonic acid as a hardening agent. Although this method has a good disintegration property of the mold after casting, it has the disadvantage that the sulfonic acid group in the hardening agent decomposes during casting and generates sulfur dioxide gas, etc., which worsens the working environment. Another method using an organic binder is a modeling method in which a benzyl ether type phenol resin and a polyisocyanate liquid are cured with amines. This method shortens the modeling time and has good workability, but it is difficult to use because of the nitrogen content caused by the polyisocyanate. becomes nitrogen gas during casting, which tends to cause pinholes in the casting. In addition, as a method that does not contain nitrogen, a mold molding method using resol type phenolic resin and organic ester as a binder is published in Japanese Patent Publication No. 61-43132 and Japanese Patent Publication No. 61-37032.
is shown. However, this method has the problem that the obtained mold has extremely low strength, requires a large amount of binder, and its uses are limited. [Purpose of the Invention] As a result of various studies on phenolic resins for mold making using organic esters as curing catalysts, the present inventor found that resol-type polyphenolic resins obtained using polyvalent phenols can produce molds with excellent strength. We found that it is particularly effective for Furthermore, based on this knowledge, we proceeded with the study and completed the present invention. [Structure of the Invention] The present invention provides a binder composition for use in a room-temperature curing mold forming method using a resin and an organic ester, wherein the resin is a resol type polyphenolic resin. A binder composition. Here, the resol type polyhydric phenol resin is a liquid resin obtained by reacting polyhydric phenol and formaldehyde using an alkaline catalyst. Polyhydric phenols are phenols having two or more hydroxyl groups, such as catechol, resorcinol, hydroquinone, pyrogallol, oxyhydroquinone, and phloroglycin, and these can be used alone or in combination. Formaldehyde is usually used in the form of formalin. The molar ratio of formaldehyde to polyhydric phenols is 0.5 to 3.0. The alkaline substances used as catalysts are usually hydroxides or oxides of alkali metals or alkaline earth metals such as potassium hydroxide, sodium hydroxide, lithium hydroxide, calcium hydroxide, etc. Used at a ratio of 0.2 to 2.0. In addition, apply a silane coupling agent such as γ-glycidoxypropyltrimethoxysilane or γ-aminopropyltriethoxysilane to the resin at a rate of 0.2
By adding and mixing ~3.0% by weight, a mold with even higher strength can be obtained. The resol type polyhydric phenol resin of the present invention can be used alone or in combination with a normal resol type phenol resin. Organic esters used as curing catalysts include methyl formate, ethyl formate, propyl formate, butyrolactone, ethylene glycol diacetate, triacetin, and the like. The organic ester can be added at the time of mixing the sand and resin, or it can be gasified and added to the mixture of sand and resin. The ratio of organic ester to phenolic resin is suitably 0.1 to 0.5 in terms of weight ratio. If it is less than 0.1, the curing of the phenolic resin will be insufficient, and if it exceeds 0.5, the degree of curing will not increase. Foundry sand includes silica sand, zircon sand, chromite sand,
Olivine sand and recycled sand can be used. Appropriate weight ratios of the resin and organic ester to the foundry sand are 0.005 to 0.04 and 0.001 to 0.02, respectively. [Effects of the Invention] According to the present invention, a mold with high strength and few gas defects can be obtained, so it is extremely suitable as an industrial mold making method. [Example] Hereinafter, the present invention will be explained with reference to Examples. The invention is not limited by the examples. Further, "parts" and "%" shown in Examples, Comparative Examples, and Application Examples are all parts by weight and weight %. Example 1 1000 parts of resorcinol and 1474 parts of 37% formalin were placed in a reaction vessel equipped with a cooler and a stirrer and heated to 60°C.
heated to. Next, add 610 parts of 50% potassium hydroxide aqueous solution to 30
Added in portions. The temperature of the reaction solution was raised to 75-80°C, and the reaction was carried out until the resin viscosity reached 2.5-3.0 poise/25°C. After reaching a predetermined viscosity, the mixture was quickly cooled to 30°C or lower, and 30 parts of γ-aminopropyltriethoxysilane were added and mixed to obtain 3030 parts of a resol-type resorcinol resin with a viscosity of 3.0 poise/25°C. Example 2 A reaction was carried out in the same manner as in Example 1 except that 500 parts of resorcin and 500 parts of catechol were used to obtain 3040 parts of a resol type resorcin/catechol resin having a viscosity of 3.2 poise/25°C. Comparative example: 1,000 parts of phenol and 1,725 parts of 37% formalin were placed in a reaction vessel equipped with a cooler and a stirrer, and the temperature was heated to 60°C.
heated to. Next, add 715 parts of 50% potassium hydroxide aqueous solution to 30
Added in portions. The temperature of the reaction solution was raised to 75-80°C, and the reaction was carried out until the resin viscosity reached 0.8-1.2 poise/25°C, and then 250 parts of water was removed under reduced pressure of 70 Torr. Thereafter, the mixture was quickly cooled to 30°C or lower, and 32 parts of γ-aminopropyltriethoxysilane were added and mixed to obtain 3200 parts of a resol type phenolic resin having a viscosity of 3.0 poise/25°C. Application example: Fremantle silica sand 3000 in Shinagawa tabletop mixer
After mixing for 30 seconds, the resin of Example 1, Example 2 or Comparative Example was added.
60 parts were added and mixed for 60 seconds to prepare mixed sand. Immediately after mixing, the mixed sand was placed in a wooden mold with a 50 mm diameter and 50 mm height mold and was hammered with a plastic hammer.
After pounding, excess sand was removed to smooth the top surface of the shaped mixed sand. After the mixed sand had hardened in the wooden mold, the mold was removed and the compressive strength was measured. The results are shown in Table 1.
【表】
第1表に示すように、本発明の鋳型用粘結剤組
成物は強度の大きい鋳型を提供するものである。[Table] As shown in Table 1, the mold binder composition of the present invention provides a mold with high strength.
Claims (1)
を使用する常温硬化型鋳型造型方法に用いる粘結
剤組成物において、前記樹脂は、フエノールとし
て多価フエノールを使用し、反応触媒としてアル
カリ金属又はアルカリ土類金属の水酸化物又は酸
化物を前記多価フエノールに対してモル比で0.2
〜2.0の割合で使用して得られたレゾール型フエ
ノール樹脂であることを特徴とする鋳型用粘結剤
組成物。 2 前記多価フエノールが、カテコール、レゾル
シン、ハイドロキノン、ピロガロール、オキシハ
イドロキノン、フロログリシンから選ばれた一種
以上であることを特徴とする特許請求の範囲第1
項記載の鋳型用粘結剤組成物。[Scope of Claims] 1. In a binder composition used in a room temperature curing mold making method using a resol type phenolic resin and an organic ester, the resin uses a polyhydric phenol as the phenol and an alkali as a reaction catalyst. The molar ratio of metal or alkaline earth metal hydroxide or oxide to the polyhydric phenol is 0.2.
A binder composition for molds, characterized in that it is a resol type phenolic resin obtained by using the resin at a ratio of ~2.0. 2. Claim 1, wherein the polyvalent phenol is one or more selected from catechol, resorcinol, hydroquinone, pyrogallol, oxyhydroquinone, and phloroglycin.
The binder composition for molds as described in 2.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32545687A JPH01166853A (en) | 1987-12-24 | 1987-12-24 | Bond composition for mold |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32545687A JPH01166853A (en) | 1987-12-24 | 1987-12-24 | Bond composition for mold |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01166853A JPH01166853A (en) | 1989-06-30 |
JPH0318531B2 true JPH0318531B2 (en) | 1991-03-12 |
Family
ID=18177070
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP32545687A Granted JPH01166853A (en) | 1987-12-24 | 1987-12-24 | Bond composition for mold |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01166853A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2162837T3 (en) * | 1993-01-05 | 2002-01-16 | Kao Corp | LIGHT COMPOSITION FOR MOLDS AND MOLD PRODUCTION METHODS. |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56102343A (en) * | 1980-01-18 | 1981-08-15 | Hitachi Chem Co Ltd | Production of mold |
-
1987
- 1987-12-24 JP JP32545687A patent/JPH01166853A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56102343A (en) * | 1980-01-18 | 1981-08-15 | Hitachi Chem Co Ltd | Production of mold |
Also Published As
Publication number | Publication date |
---|---|
JPH01166853A (en) | 1989-06-30 |
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