JPH04118146A - Binder composition for molding sand - Google Patents
Binder composition for molding sandInfo
- Publication number
- JPH04118146A JPH04118146A JP23641090A JP23641090A JPH04118146A JP H04118146 A JPH04118146 A JP H04118146A JP 23641090 A JP23641090 A JP 23641090A JP 23641090 A JP23641090 A JP 23641090A JP H04118146 A JPH04118146 A JP H04118146A
- Authority
- JP
- Japan
- Prior art keywords
- mold
- binder composition
- phosphoric
- weight
- parts
- 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
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 24
- 239000011230 binding agent Substances 0.000 title claims abstract description 23
- 239000003110 molding sand Substances 0.000 title abstract description 5
- 239000005011 phenolic resin Substances 0.000 claims abstract description 19
- 150000002895 organic esters Chemical class 0.000 claims abstract description 12
- 150000005691 triesters Chemical class 0.000 claims abstract description 5
- 239000004576 sand Substances 0.000 claims description 20
- 150000002148 esters Chemical class 0.000 abstract description 3
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 abstract description 2
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 abstract 1
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 description 26
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 25
- 238000004519 manufacturing process Methods 0.000 description 8
- -1 phosphoric acid triesters Chemical class 0.000 description 8
- 229920001568 phenolic resin Polymers 0.000 description 7
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 239000008187 granular material Substances 0.000 description 6
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 5
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 5
- 229910019142 PO4 Inorganic materials 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
- 238000005266 casting Methods 0.000 description 4
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 4
- 239000010452 phosphate Substances 0.000 description 4
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 4
- 229930185605 Bisphenol Natural products 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
- 238000010367 cloning Methods 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 239000006087 Silane Coupling Agent Substances 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 235000013773 glyceryl triacetate Nutrition 0.000 description 2
- 239000001087 glyceryl triacetate Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- IXQGCWUGDFDQMF-UHFFFAOYSA-N o-Hydroxyethylbenzene Natural products CCC1=CC=CC=C1O IXQGCWUGDFDQMF-UHFFFAOYSA-N 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 229960002622 triacetin Drugs 0.000 description 2
- JTXMVXSTHSMVQF-UHFFFAOYSA-N 2-acetyloxyethyl acetate Chemical compound CC(=O)OCCOC(C)=O JTXMVXSTHSMVQF-UHFFFAOYSA-N 0.000 description 1
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 1
- HXDLWJWIAHWIKI-UHFFFAOYSA-N 2-hydroxyethyl acetate Chemical compound CC(=O)OCCO HXDLWJWIAHWIKI-UHFFFAOYSA-N 0.000 description 1
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- VEZXCJBBBCKRPI-UHFFFAOYSA-N beta-propiolactone Chemical compound O=C1CCO1 VEZXCJBBBCKRPI-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 125000000853 cresyl group Chemical group C1(=CC=C(C=C1)C)* 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000009970 fire resistant effect Effects 0.000 description 1
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229960004337 hydroquinone Drugs 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 229960001553 phloroglucinol Drugs 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 238000005987 sulfurization reaction Methods 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
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Mold Materials And Core Materials (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、自硬性鋳型及びガス硬化性鋳型造型法に用い
られる鋳物砂用粘結剤組成物に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a binder composition for foundry sand used in self-hardening molds and gas-hardening mold making methods.
更に詳しくは、水溶性フェノール樹脂を粘結剤として用
い、これを有機エステルにより硬化させる鋳型造型法に
用いられる改良された有機エステル硬化型跡物砂用粘結
剤組成物に関するものである。More specifically, the present invention relates to an improved binder composition for organic ester-cured trace sand used in a mold making method that uses a water-soluble phenol resin as a binder and cures it with an organic ester.
有機粘結剤を用いて主型や中子のような鋳型を製造する
造型法として、自硬性鋳型法、コールドボックス鋳型法
、クローニング法(シェル法)は公知である。特に有機
自硬性鋳型造型法は機械鋳物分野を中心に生産性、鋳物
品質、安全衛生上の観点から無機系に代わって既に汎用
的な造型法となっている。The self-hardening mold method, the cold box mold method, and the cloning method (shell method) are known as molding methods for producing molds such as main molds and cores using organic binders. In particular, organic self-hardening mold making methods have already become a general-purpose molding method, replacing inorganic ones, from the viewpoints of productivity, quality of castings, and safety and health, mainly in the field of mechanical casting.
一方、従来、中、高速で鋳型を製造するにはフェノール
樹脂を粒状耐火物に被覆した、いわゆるコーテツドサン
ドを加熱硬化して鋳型を製造するクローニング法が幅広
く使用されている。On the other hand, conventionally, in order to manufacture molds at medium to high speeds, a cloning method has been widely used in which molds are manufactured by heating and hardening so-called coated sand, in which granular refractories are coated with phenolic resin.
しかし、鋳型製造時の省エネルギー、鋳型生産速度、更
に鋳型、鋳物の品質を改善するために、ガス状又はエロ
ゾル状物質で常温硬化させるコールドボックス鋳型法が
クローニング法を代替する鋳型の製造法として鋳物業界
で真剣に導入が試みられてきている。However, in order to save energy during mold manufacturing, mold production speed, and improve the quality of molds and castings, the cold box molding method, in which gaseous or aerosol substances are used to cure at room temperature, has replaced the cloning method. The industry is seriously trying to introduce it.
〔発明が解決しようとする課題し
有機自硬性鋳型造型法及びガス硬化性鋳型造型性に用い
られる粘結剤組成物として、水溶性フェノール−ホルム
アルデヒド樹脂水溶液を粘結剤とし、これを有機エステ
ルで硬化せしめる鋳物砂用粘結剤組成物が、特開昭50
−130627号公報、特開昭58−154433号公
報や特開昭58−154434号公報により公知である
。[The problem to be solved by the invention is to use a water-soluble phenol-formaldehyde resin aqueous solution as a binder as a binder composition used in an organic self-hardening mold making method and a gas hardening mold making method, and to use an organic ester as a binder composition. A hardening binder composition for foundry sand was published in Japanese Patent Application Laid-Open No. 1985.
It is publicly known from Japanese Patent Application Laid-open No. 130627, Japanese Patent Application Laid-Open No. 58-154433, and Japanese Patent Application Laid-open No. 154434-1987.
この粘結剤を用いた鋳型造型法は粘結剤中に硫黄原子を
含まないため酸硬化性樹脂を用いた鋳型造型法に比較し
て浸硫の傾向が小さい等の長所を有するが、反面酸硬化
性鋳型造型法に比較して、鋳型強度が低い、可使時間が
短い、砂再生性が劣るなどの欠点を有しており、更にそ
の改良が望まれている。This mold making method using a binder does not contain sulfur atoms in the binder, so it has the advantage of being less prone to sulfurization than the mold making method using acid-curing resins. Compared to the acid-curing mold making method, this method has disadvantages such as low mold strength, short pot life, and poor sand regeneration properties, and further improvements are desired.
本発明者らは上記問題点を解決すべく鋭意研究の結果、
水溶性フェノール樹脂を粘結剤とし、これを有機エステ
ルにより硬化させる鋳型造型法に用いられる鋳物砂用粘
結剤組成物において、水溶性フェノール樹脂に特定のリ
ン酸エステル類の1種又は2種以上を併用してなる鋳物
砂用粘結剤組成物を使用することにより、鋳型強度を大
幅に向上させることを見出し、本発明を完成するに到っ
た。As a result of intensive research by the present inventors to solve the above problems,
In a binder composition for foundry sand used in a mold making method in which a water-soluble phenol resin is used as a binder and the binder is hardened with an organic ester, one or two specific phosphate esters are added to the water-soluble phenol resin. The present inventors have discovered that mold strength can be significantly improved by using a binder composition for foundry sand that uses the above components in combination, and have completed the present invention.
即ち本発明は、水溶性フェノール樹脂とリン酸トリエス
テル類の1種又は2種以上とを必須成分とすることを特
徴とする有機エステル硬化型鋳物砂用粘結剤組成物に関
するものである。That is, the present invention relates to an organic ester-curable binder composition for foundry sand, which contains a water-soluble phenol resin and one or more kinds of phosphoric triesters as essential components.
本発明において用いられるリン酸トリエステル類として
、具体的には次の様なものが挙げられる。Specifically, the phosphoric acid triesters used in the present invention include the following.
リン酸トリメチルエステノベ リン酸トリエチルエステ
ル、リン酸トリブチルエステル、リン酸トリブトキシエ
チルエステノベリン酸トリフェニルエステノペ リン酸
トリスイソプロピルフェニルエステル、リン酸トリクレ
ジノベ リン酸トリ2−エチルヘキシル等である。Trimethyl ester phosphate, tributyl phosphate, tributoxyethyl ester phosphate, triphenylestenoperic acid, trisisopropylphenyl ester, tricrezino phosphate, tri2-ethylhexyl phosphate, and the like.
本発明の粘結剤組成物を用いることにより、鋳型強度を
大幅に改善し得る理由は次の如く推定される。即ち、上
記の如きリン酸トリエステル類の1種又は2種以上を存
在させることにより、耐火性粒状材料と水溶性フェノー
ル樹脂との表面水素結合を誘起して、界面接着性の改善
等の表面特性を化学的に向上せしめたこと、また硬化鋳
型の組成物界面、即ち固体−液体、液体−液体界面への
浸透性及び拡散性と耐火性粒子に対する凝集力等の特性
とを物理的に改善、改質し、向上せしめたことによると
考えられる。The reason why mold strength can be significantly improved by using the binder composition of the present invention is presumed to be as follows. That is, the presence of one or more of the above-mentioned phosphoric acid triesters induces surface hydrogen bonding between the fire-resistant granular material and the water-soluble phenolic resin, thereby improving surface adhesion, etc. Chemically improved properties, as well as physically improved properties such as permeability and diffusivity to composition interfaces, i.e., solid-liquid and liquid-liquid interfaces, and cohesive strength for refractory particles, of the hardened mold. This is thought to be due to the fact that it has been modified and improved.
水溶性フェノール樹脂と上記の如きリン酸トリエステル
類の1種又は2種以上の混合物とを併用する形態として
は、水溶性フェノール樹脂又は水溶液中に含有させても
よいし、有機エステル中に攪拌混合せしめてもよいし、
或いはそれらと別途に耐火性粒状材料に添加してもよい
。When using a water-soluble phenol resin and one type or a mixture of two or more of the above-mentioned phosphoric acid triesters, they may be contained in the water-soluble phenol resin or an aqueous solution, or they may be stirred into the organic ester. It may be mixed,
Alternatively, they may be added separately to the refractory granular material.
またこの際、周知の溶媒に希釈して混練性を高めて添加
することもできる。In addition, at this time, it can be diluted with a well-known solvent to improve kneadability and then added.
゛本発明の有機エステル硬化型鋳物砂用粘結剤組成物を
用いて鋳物用砂型を自硬性鋳型造型法によって製造する
には、耐火性粒状材料100重量部に、硬化剤である有
機エステル0.05〜9重量部、好ましくは0.1〜5
重量部、水溶性フェノール樹脂水溶液を固形分として0
.4〜15重量部、好ましくは0.6〜5重量部及びリ
ン酸トリエステル類0.01〜5重量部、好ましくは0
.05〜3重量部を周知の方法で混練し、従来の自硬性
鋳型製造プロセスをそのまま利用して鋳型を製造するこ
とができる。゛In order to manufacture a foundry sand mold by the self-hardening mold making method using the organic ester hardening type molding sand binder composition of the present invention, 0 parts by weight of the organic ester as a hardening agent is added to 100 parts by weight of the refractory granular material. .05 to 9 parts by weight, preferably 0.1 to 5 parts by weight
Parts by weight, solid content of water-soluble phenol resin aqueous solution: 0
.. 4 to 15 parts by weight, preferably 0.6 to 5 parts by weight and 0.01 to 5 parts by weight, preferably 0
.. A mold can be manufactured by kneading 05 to 3 parts by weight by a well-known method and using the conventional self-hardening mold manufacturing process as is.
また、本発明において、鋳物用砂型をガス硬化性鋳型造
型法によって製造するには、まず耐火性粒状材料100
重量部に、水溶性フェノール樹脂水溶液を固形分として
0.4〜15重量部、好ましくは0.6〜5重量部及び
リン酸トリエステル類0.01〜5重量部、好ましくは
0.05〜3重量部を加えた混練砂を手込め、もしくは
加圧空気でのブローイングにより模型中に充填し、次い
でガス状もしくはエロゾル状の有機エステル0.05〜
9重量部を吹き込んでフェノール樹脂混合物を硬化させ
ることにより、鋳型を製造する。In addition, in the present invention, in order to manufacture a foundry sand mold by a gas hardening mold making method, first, 100 pieces of refractory granular material are used.
The solid content of the water-soluble phenol resin aqueous solution is 0.4 to 15 parts by weight, preferably 0.6 to 5 parts by weight, and 0.01 to 5 parts by weight of phosphoric acid triesters, preferably 0.05 to 5 parts by weight. Mixed sand containing 3 parts by weight is filled into the model by hand or by blowing with pressurized air, and then 0.05 to 0.05 parts by weight of organic ester in gaseous or aerosol form is added.
A mold is made by curing the phenolic resin mixture by blowing in 9 parts by weight.
本発明に用いられる有機エステルとしては、ラクトン類
或いは炭素数1〜10の一価又は多価アルコールと炭素
数1〜10の有機カルボン酸より誘導される有機エステ
ルの単独もしくは混合物が用いられるが、自硬性鋳型造
型法ではT−ブチロラクトン、プロピオンラクトン、ε
−カプロラクトン、ギ酸エチノペエチレングリコールジ
アセテート、エチレングリコールモノアセテート、トリ
アセチン等を用いるのが好ましく、ガス硬化性鋳型造型
法ではギ酸メチルを用いるのが好ましい。As the organic ester used in the present invention, organic esters derived from lactones or monohydric or polyhydric alcohols having 1 to 10 carbon atoms and organic carboxylic acids having 1 to 10 carbon atoms may be used alone or in mixtures. In the self-hardening mold making method, T-butyrolactone, propionolactone, ε
- It is preferable to use caprolactone, ethinope formate, ethylene glycol diacetate, ethylene glycol monoacetate, triacetin, etc., and it is preferable to use methyl formate in the gas-curable mold making method.
本発明に用いられる水溶性フェノール樹脂とは有機エス
テルで硬化可能な樹脂であり、例えばフエノーノペクレ
ゾーノペレゾルシノーノヘキシレノール、ビスフェノー
ルA1クミルフエノーノペノニルフエノーノベブチルフ
エノーノベフエニルフエノーノベエチルフエノール、オ
クチルフエノーノペアミルフェノーノペナフトール、ビ
スフェノールF1ビスフエノール01カテコーノベハイ
ドロキノン、ピロガロール、フロログルシン、リグニン
、ビスフェノールA残渣、クレゾール残渣、クロロフェ
ノール、ジクロロフェノーノベその他の置換フェノール
を含めたフェノール類と、ホルムアルデヒド、アセトア
ルデ巳ド、フルフラールアルデヒド及びアルデヒドの混
合物等との反応によって得られるフェノール樹脂が挙げ
られる。これらのフェノール樹脂の縮合に用いられる適
当なアルカリ性物質は水酸化ナトリウム、水酸化カリウ
ム、水酸化リチウム及びこれらの混合物であるが、水酸
化カリウムが最も好ましい。The water-soluble phenolic resin used in the present invention is a resin that can be cured with an organic ester, such as phenonopecresonoperesorcinonohexylenol, bisphenol A1 cumylphenonopenonylphenonobebutylphenonobephenyl. Including phenonobe ethylphenol, octylphenonopea milphenonopenaphthol, bisphenol F1 bisphenol 01 catechonobe hydroquinone, pyrogallol, phloroglucin, lignin, bisphenol A residue, cresol residue, chlorophenol, dichlorophenonobe and other substituted phenols. Examples include phenolic resins obtained by reacting phenols with formaldehyde, acetaldehyde, furfuraldehyde, a mixture of aldehydes, and the like. Suitable alkaline materials used in the condensation of these phenolic resins are sodium hydroxide, potassium hydroxide, lithium hydroxide and mixtures thereof, with potassium hydroxide being most preferred.
耐火性粒状材料としては、石英質を主成分とする珪砂の
他、クロマイト砂、ジルコン砂、オリピン砂、アルミナ
サンド等の無機耐火性粒状材料が使用されるが、特に限
定されるものではない。As the refractory granular material, inorganic refractory granular materials such as chromite sand, zircon sand, oripin sand, alumina sand, etc., as well as silica sand containing quartz as a main component, are used, but are not particularly limited.
また、更に鋳型強度を向上させる目的でシランカップリ
ング剤を加えても差し支えない。好ましいシランカップ
リング剤としては、T−アミノプロピルトリエトキシシ
ランやT−(2アミノエチル)アミノプロピルトリメト
キシシラン等が挙げられる。Furthermore, a silane coupling agent may be added for the purpose of further improving mold strength. Preferred silane coupling agents include T-aminopropyltriethoxysilane and T-(2-aminoethyl)aminopropyltrimethoxysilane.
以下、実施例をもって本発明の詳細な説明するが、本発
明はこれらの実施例のみに限定されるものではない。Hereinafter, the present invention will be explained in detail with reference to Examples, but the present invention is not limited only to these Examples.
実施例1〜6及び比較例1
自硬性鋳型造型法における鋳型強度の経時変化を評価し
た。Examples 1 to 6 and Comparative Example 1 Changes in mold strength over time in a self-hardening mold making method were evaluated.
即ち、珪砂100重量部に対して、トリアセチンを0.
25重量部、水溶性フェノール樹脂を1.5重量部及び
表−1に示すリン酸トリエステル類を0.15重量部添
加混練してなる混合物を、直径が53mmで高さが5Q
mmであるテストピース用模型に充填し、混練後の圧縮
強度の経時変化を測定した。That is, 0.0% triacetin was added to 100 parts by weight of silica sand.
A mixture of 25 parts by weight, 1.5 parts by weight of water-soluble phenol resin, and 0.15 parts by weight of the phosphoric acid triesters shown in Table 1 was kneaded into a mold with a diameter of 53 mm and a height of 5Q.
The mixture was filled into a test piece model having a diameter of 1 mm, and the change in compressive strength over time after kneading was measured.
結果を表−1に示す。The results are shown in Table-1.
表
実施例7〜12及び比較例2
ガス硬化性鋳型造型法における鋳型強度の経時変化を評
価した。Table Examples 7 to 12 and Comparative Example 2 Changes in mold strength over time in the gas hardening mold making method were evaluated.
即ち、珪砂100重量部に対し、固形分50重量%であ
る水溶性フェノール樹脂を2.0重量部、表−2に示す
各種リン酸トリエステル類を0.2重量部添加混練して
なる混合物を、直径が50mmで高さが5Qmmである
ガス硬化用テストピース模型に充填した。この模型中に
3.0重量部のガス状のギ酸メチルを注入し、注入後の
圧縮強度の経時変化を測定した。That is, a mixture obtained by adding and kneading 2.0 parts by weight of a water-soluble phenol resin having a solid content of 50% by weight and 0.2 parts by weight of various phosphoric triesters shown in Table 2 to 100 parts by weight of silica sand. was filled into a gas curing test piece model having a diameter of 50 mm and a height of 5 Q mm. 3.0 parts by weight of gaseous methyl formate was injected into this model, and the change in compressive strength over time after the injection was measured.
結果を表−2に示す。The results are shown in Table-2.
表
〔発明の効果〕
上記の実施例で明白なように、本発明の製造方法によれ
ば、従来の製造方法によって得られる鋳型に比べ高強度
の鋳型が得られる。Table [Effects of the Invention] As is clear from the above examples, according to the manufacturing method of the present invention, a mold having higher strength can be obtained than a mold obtained by a conventional manufacturing method.
その結果、粘結剤の使用量の低減が可能となるため、鋳
物砂の回収が容易となり、また、鋳込時の鋳型から発生
するガス量を減少し得るので、ガス欠陥の発生を抑制し
健全な鋳物が製造でき、実用上有益なものとなる。As a result, the amount of binder used can be reduced, making it easier to recover molding sand, and the amount of gas generated from the mold during pouring can be reduced, suppressing the occurrence of gas defects. Sound castings can be produced, which is useful for practical purposes.
Claims (1)
種又は2種以上とを必須成分とすることを特徴とする有
機エステル硬化型鋳物砂用粘結剤組成物。 2 有機エステルがガス状であることを特徴とする請求
項1記載の鋳物砂用粘結剤組成物。[Claims] 1. 1. Water-soluble phenol resin and phosphoric triester.
An organic ester-curing binder composition for foundry sand, characterized in that it contains one or more species as essential components. 2. The binder composition for foundry sand according to claim 1, wherein the organic ester is gaseous.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23641090A JP2892468B2 (en) | 1990-09-05 | 1990-09-05 | Binder composition for foundry sand |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23641090A JP2892468B2 (en) | 1990-09-05 | 1990-09-05 | Binder composition for foundry sand |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04118146A true JPH04118146A (en) | 1992-04-20 |
JP2892468B2 JP2892468B2 (en) | 1999-05-17 |
Family
ID=17000346
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP23641090A Expired - Fee Related JP2892468B2 (en) | 1990-09-05 | 1990-09-05 | Binder composition for foundry sand |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2892468B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009126958A (en) * | 2007-11-26 | 2009-06-11 | Sumitomo Bakelite Co Ltd | Resol type phenolic resin composition and abrasive cloth and paper using the same |
-
1990
- 1990-09-05 JP JP23641090A patent/JP2892468B2/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009126958A (en) * | 2007-11-26 | 2009-06-11 | Sumitomo Bakelite Co Ltd | Resol type phenolic resin composition and abrasive cloth and paper using the same |
Also Published As
Publication number | Publication date |
---|---|
JP2892468B2 (en) | 1999-05-17 |
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