JPH04118150A - Binder composition for molding sand - Google Patents
Binder composition for molding sandInfo
- Publication number
- JPH04118150A JPH04118150A JP23641490A JP23641490A JPH04118150A JP H04118150 A JPH04118150 A JP H04118150A JP 23641490 A JP23641490 A JP 23641490A JP 23641490 A JP23641490 A JP 23641490A JP H04118150 A JPH04118150 A JP H04118150A
- Authority
- JP
- Japan
- Prior art keywords
- alcohol
- binder composition
- mold
- 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 27
- 239000011230 binding agent Substances 0.000 title claims abstract description 25
- 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 14
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 10
- 125000003118 aryl group Chemical group 0.000 claims abstract description 3
- 239000004576 sand Substances 0.000 claims description 22
- 150000001298 alcohols Chemical class 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000004615 ingredient Substances 0.000 claims 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 abstract description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract description 5
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 abstract description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 abstract description 4
- 229940035429 isobutyl alcohol Drugs 0.000 abstract description 2
- 239000000463 material Substances 0.000 abstract description 2
- 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
- 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
- 238000005266 casting Methods 0.000 description 5
- 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
- 238000004898 kneading Methods 0.000 description 4
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 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
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 3
- 238000010367 cloning Methods 0.000 description 3
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- -1 octylphenol Chemical compound 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- OOCCDEMITAIZTP-QPJJXVBHSA-N (E)-cinnamyl alcohol Chemical compound OC\C=C\C1=CC=CC=C1 OOCCDEMITAIZTP-QPJJXVBHSA-N 0.000 description 2
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
- GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical compound CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 2
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- 239000006087 Silane Coupling Agent Substances 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- 239000001087 glyceryl triacetate Substances 0.000 description 2
- 235000013773 glyceryl triacetate Nutrition 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 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
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 229960002622 triacetin Drugs 0.000 description 2
- KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 2
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
- UMPSXRYVXUPCOS-UHFFFAOYSA-N 2,3-dichlorophenol Chemical compound OC1=CC=CC(Cl)=C1Cl UMPSXRYVXUPCOS-UHFFFAOYSA-N 0.000 description 1
- CJWNFAKWHDOUKL-UHFFFAOYSA-N 2-(2-phenylpropan-2-yl)phenol Chemical compound C=1C=CC=C(O)C=1C(C)(C)C1=CC=CC=C1 CJWNFAKWHDOUKL-UHFFFAOYSA-N 0.000 description 1
- WCASXYBKJHWFMY-NSCUHMNNSA-N 2-Buten-1-ol Chemical compound C\C=C\CO WCASXYBKJHWFMY-NSCUHMNNSA-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
- 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
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- MEEKGULDSDXFCN-UHFFFAOYSA-N 2-pentylphenol Chemical compound CCCCCC1=CC=CC=C1O MEEKGULDSDXFCN-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- OOCCDEMITAIZTP-UHFFFAOYSA-N allylic benzylic alcohol Natural products OCC=CC1=CC=CC=C1 OOCCDEMITAIZTP-UHFFFAOYSA-N 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
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 125000000853 cresyl group Chemical group C1(=CC=C(C=C1)C)* 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- XCIXKGXIYUWCLL-UHFFFAOYSA-N cyclopentanol Chemical compound OC1CCCC1 XCIXKGXIYUWCLL-UHFFFAOYSA-N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 1
- WCASXYBKJHWFMY-UHFFFAOYSA-N gamma-methylallyl alcohol Natural products CC=CCO WCASXYBKJHWFMY-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
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- PHQOGHDTIVQXHL-UHFFFAOYSA-N n'-(3-trimethoxysilylpropyl)ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCN PHQOGHDTIVQXHL-UHFFFAOYSA-N 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 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
- TVDSBUOJIPERQY-UHFFFAOYSA-N prop-2-yn-1-ol Chemical compound OCC#C TVDSBUOJIPERQY-UHFFFAOYSA-N 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
- 239000002904 solvent Substances 0.000 description 1
- 238000009987 spinning Methods 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
- 229940057402 undecyl alcohol Drugs 0.000 description 1
- 125000002256 xylenyl group Chemical class C1(C(C=CC=C1)C)(C)* 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鋳物砂用粘結
剤組成物に関するものである。More specifically, the present invention relates to an improved organic ester-curing binder composition for molding sand used in a mold making method in which a water-soluble phenol resin is used as a binder and the resin is cured 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]
有機自硬性鋳型造型法及びガス硬化性鋳型造型法に用い
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58454433号公報
や特開昭58−154434号公報により公知である。[Problem to be solved by the invention] As a binder composition used in an organic self-hardening mold making method and a gas hardening mold making method, a water-soluble phenol-formaldehyde resin aqueous solution is used as a binder, and this is mixed with an organic ester. 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. 58454433, and Japanese Patent Application Laid-open No. 154434/1982.
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、砂再住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 residing 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ア
ルコール類の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 more specific alcohols are added to the water-soluble phenol resin. It has been discovered that mold strength can be significantly improved by using a binder composition for foundry sand in combination, and the present invention has been completed.
即ち本発明は、水溶性フェノール樹脂とアルコール類の
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 alcohols as essential components.
本発明において用いられるアルコール類としては、炭素
数3〜12の1価アルコール、又は分子中に芳香環を少
なくとも1個有するアルコールが好ましい。The alcohols used in the present invention are preferably monohydric alcohols having 3 to 12 carbon atoms or alcohols having at least one aromatic ring in the molecule.
本発明において用いられるアルコール類として具体的に
は、次の様なものが挙げられる。Specifically, the alcohols used in the present invention include the following.
プロピルアルコール、イソプロピルアルコール、ブチル
アルコール、イソブチルアルコール5ec−ブチルアル
コール、tert−ブチルアルコール、n−アミルアル
コール、イソアミルアルコール、ヘキシルアルコール、
ヘプチルアルコール、オクチルアルコール、カプリルア
ルコール、ノニルアルコール、デシルアルコール、ウン
デシルアルコール、ラウリルアルコール、アリルアルコ
ール、クロチルアルコール、プロパギルアルコール、シ
クロペンタノール、シクロヘキサノール、ベンジルアル
コール、シンナミルアルコール、フルフリルアルコール
等である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。Propyl alcohol, isopropyl alcohol, butyl alcohol, isobutyl alcohol, 5ec-butyl alcohol, tert-butyl alcohol, n-amyl alcohol, isoamyl alcohol, hexyl alcohol,
Heptyl alcohol, octyl alcohol, caprylic alcohol, nonyl alcohol, decyl alcohol, undecyl alcohol, lauryl alcohol, allyl alcohol, crotyl alcohol, propargyl alcohol, cyclopentanol, cyclohexanol, benzyl alcohol, cinnamyl alcohol, furfuryl alcohol The reason why mold strength can be significantly improved by using the binder composition of the present invention, which is as follows, is presumed to be as follows.
即ち、上記の如きアルコール類の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。That is, the presence of one or more of the above alcohols induces surface hydrogen bonding between the refractory granular material and the water-soluble phenolic resin, thereby chemically improving surface properties such as improving interfacial adhesion. physical improvement and modification of properties such as permeability and diffusivity to the composition interface of the hardened mold, i.e. solid-liquid, liquid-liquid interface, and cohesive force for refractory particles. This is thought to be due to the improvement in
水溶性フェノール樹脂と上記の如きアルコール類の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。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。The water-soluble phenol resin and one type or a mixture of two or more of the above-mentioned alcohols may be used together, and may be contained in the water-soluble phenol resin or an aqueous solution.
They may be stirred and mixed into the organic ester, or they may be added separately to the refractory granular material. 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重量部及びアル
コール類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 binder composition for foundry sand of the present invention, 100 parts by weight of the refractory granular material is mixed with 0.00 parts by weight of the organic ester as a hardening agent. 0.05 to 9 parts by weight, preferably 0.1 to 5 parts by weight, based on the solid content of the water-soluble phenol resin aqueous solution.
4 to 15 parts by weight, preferably 0.6 to 5 parts by weight, and 0.01 to 5 parts by weight, preferably 0.05 to 3 parts by weight of alcohol.
A mold can be manufactured by kneading the weight parts 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
アルコール類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, preferably 0.05 parts by weight of the alcohol.
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 9 parts by weight of organic ester in gaseous or aerosol form is blown into the phenolic resin mixture. A mold is produced by curing.
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γブチロラクトン、プロピオンラクトン、ε−
カプロラクトン、ギ酸エチル、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, γ-butyrolactone, propionolactone, ε-
It is preferable to use caprolactone, ethyl 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、例えばフェノール、クレ
ゾール、レゾルシノール、キシレノール、ビスフェノー
ルA、クミルフェノール、ノニルフェノール、ブチルフ
ェノール、フェニルフェノール、エチルフェノール、オ
クチルフェノール、アミルフェノール、ナフトール、ビ
スフェノールF、ビスフェノールC1カテコール、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、ジクロロフェノール、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
ルデヒド、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7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 phenol, cresol, resorcinol, xylenol, bisphenol A, cumylphenol, nonylphenol, butylphenol, phenylphenol, ethylphenol, octylphenol, amylphenol, etc. Phenols, including phenol, naphthol, bisphenol F, bisphenol C1 catechol, hydroquinone, pyrogallol, phloroglucin, lignin, bisphenol A residue, cresol residue, chlorophenol, dichlorophenol, and other substituted phenols, as well as formaldehyde, acetaldehyde, furfuraldehyde, and Examples include phenolic resins obtained by reaction with mixtures of aldehydes and the like. Suitable alkaline materials used in the condensation of these phenolic resins are sodium hydroxide, potassium hydroxide, lithium heptahydroxide, 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、γ−アミノプロピルトリエトキシシ
ランやγ−(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 γ-aminopropyltriethoxysilane and γ-(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1〜7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 7 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に示す各種アルコール類を0.15重量部添加混
練してなる混合物を、直径が50mmで高さが50mm
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 obtained by adding and kneading 25 parts by weight, 1.5 parts by weight of a water-soluble phenol resin, and 0.15 parts by weight of various alcohols shown in Table 1 was prepared into a mixture having a diameter of 50 mm and a height of 50 mm.
The mixture was filled into a test piece model, 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8〜14及び比較例2
ガス硬化性鋳型造型法における紡型強度の経時変化を評
価した。Table Examples 8 to 14 and Comparative Example 2 Changes in spinning mold strength over time in the gas hardening mold making method were evaluated.
即ち、珪砂1003!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
す各種アルコール類を0.2重量部添加混練してなる混
合物を、直径が5oIllI11で高さが50sua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, silica sand 1003! A mixture obtained by adding and kneading 2.0 parts by weight of a water-soluble phenol resin with a solid content of 50% by weight and 0.2 parts by weight of various alcohols shown in Table 2 was mixed with a diameter of 5oIllI11 and a high It was filled into a gas curing test piece model having a diameter of 50 sua. 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, it is possible to reduce the amount of binder used, making it easier to recover molding sand, and also reducing the amount of gas generated from the mold during casting, thereby suppressing the occurrence of gas defects. Sound castings can be produced and are useful for practical purposes.
Claims (1)
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 アルコール類が炭素数3〜12の1価アルコールで
ある請求項1記載の鋳物砂用粘結剤組成物。 3 アルコール類が分子中に少なくとも1個の芳香環を
有する請求項1又は2記載の鋳物砂用粘結剤組成物。 4 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. One or two water-soluble phenol resins and alcohols.
An organic ester hardening type binder composition for foundry sand, characterized in that the organic ester hardening type binder composition contains at least one of the above essential ingredients. 2. The binder composition for foundry sand according to claim 1, wherein the alcohol is a monohydric alcohol having 3 to 12 carbon atoms. 3. The binder composition for foundry sand according to claim 1 or 2, wherein the alcohol has at least one aromatic ring in the molecule. 4. 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 |
---|---|---|---|
JP23641490A JP2892471B2 (en) | 1990-09-05 | 1990-09-05 | Binder composition for foundry sand |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23641490A JP2892471B2 (en) | 1990-09-05 | 1990-09-05 | Binder composition for foundry sand |
Publications (2)
Publication Number | Publication Date |
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JPH04118150A true JPH04118150A (en) | 1992-04-20 |
JP2892471B2 JP2892471B2 (en) | 1999-05-17 |
Family
ID=17000406
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Cited By (1)
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---|---|---|---|---|
CN115741908A (en) * | 2022-11-22 | 2023-03-07 | 广东东方广厦模块化建筑有限公司 | Corrosion-resistant plywood and preparation method thereof |
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1990
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Cited By (1)
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CN115741908A (en) * | 2022-11-22 | 2023-03-07 | 广东东方广厦模块化建筑有限公司 | Corrosion-resistant plywood and preparation method thereof |
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