JPH04371343A - Binder composition for sand core for high-pressure casting - Google Patents
Binder composition for sand core for high-pressure castingInfo
- Publication number
- JPH04371343A JPH04371343A JP14873791A JP14873791A JPH04371343A JP H04371343 A JPH04371343 A JP H04371343A JP 14873791 A JP14873791 A JP 14873791A JP 14873791 A JP14873791 A JP 14873791A JP H04371343 A JPH04371343 A JP H04371343A
- Authority
- JP
- Japan
- Prior art keywords
- binder composition
- formalin
- weight
- sand core
- resin
- 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 32
- 239000011230 binding agent Substances 0.000 title claims abstract description 26
- 238000005266 casting Methods 0.000 title claims abstract description 22
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Natural products O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims abstract description 17
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 10
- 238000004512 die casting Methods 0.000 claims abstract description 9
- 229910001234 light alloy Inorganic materials 0.000 claims abstract description 8
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 8
- 238000004898 kneading Methods 0.000 claims abstract description 5
- 238000010438 heat treatment Methods 0.000 claims abstract description 4
- 229920005989 resin Polymers 0.000 claims description 15
- 239000011347 resin Substances 0.000 claims description 15
- 238000004519 manufacturing process Methods 0.000 claims description 8
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinyl group Chemical group C1(O)=CC(O)=CC=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 5
- 239000002516 radical scavenger Substances 0.000 claims description 5
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 claims description 4
- 150000002576 ketones Chemical class 0.000 claims description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 3
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 claims description 2
- 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 claims description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 2
- 239000004793 Polystyrene Substances 0.000 claims description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 claims description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical group C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 2
- 239000004202 carbamide Substances 0.000 claims description 2
- 229930003836 cresol Natural products 0.000 claims description 2
- 229920005610 lignin Polymers 0.000 claims description 2
- 239000003208 petroleum Substances 0.000 claims description 2
- 229920002223 polystyrene Polymers 0.000 claims description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 claims description 2
- 125000002256 xylenyl group Chemical class C1(C(C=CC=C1)C)(C)* 0.000 claims description 2
- 239000004576 sand Substances 0.000 abstract description 14
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 abstract description 6
- 150000003839 salts Chemical class 0.000 abstract description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 47
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 238000000465 moulding Methods 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 230000009970 fire resistant effect Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- 229910052845 zircon Inorganic materials 0.000 description 3
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 3
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
- XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000006087 Silane Coupling Agent Substances 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- RJDOZRNNYVAULJ-UHFFFAOYSA-L [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[F-].[F-].[Mg++].[Mg++].[Mg++].[Al+3].[Si+4].[Si+4].[Si+4].[K+] Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[F-].[F-].[Mg++].[Mg++].[Mg++].[Al+3].[Si+4].[Si+4].[Si+4].[K+] RJDOZRNNYVAULJ-UHFFFAOYSA-L 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000008119 colloidal silica Substances 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- -1 heterocyclic hydrocarbons Chemical class 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 235000013379 molasses Nutrition 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- FPZWZCWUIYYYBU-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl acetate Chemical compound CCOCCOCCOC(C)=O FPZWZCWUIYYYBU-UHFFFAOYSA-N 0.000 description 1
- NQBXSWAWVZHKBZ-UHFFFAOYSA-N 2-butoxyethyl acetate Chemical compound CCCCOCCOC(C)=O NQBXSWAWVZHKBZ-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- WHFKYDMBUMLWDA-UHFFFAOYSA-N 2-phenoxyethyl acetate Chemical compound CC(=O)OCCOC1=CC=CC=C1 WHFKYDMBUMLWDA-UHFFFAOYSA-N 0.000 description 1
- ZYAASQNKCWTPKI-UHFFFAOYSA-N 3-[dimethoxy(methyl)silyl]propan-1-amine Chemical compound CO[Si](C)(OC)CCCN ZYAASQNKCWTPKI-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
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 235000001727 glucose Nutrition 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 238000010112 shell-mould casting Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 150000005846 sugar alcohols Polymers 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
- 238000003466 welding Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、高圧で軽合金を鋳造す
るダイカストにおいてアンダーカット部に適用される砂
中子を製造する際に用いられる組成物に関するものであ
る。更に詳しくは、数10kg/cm2 〜数 100
kg/cm2 の圧力で軽合金を鋳造するダイカストに
おいてアンダーカット部に適用される砂中子を、耐火性
粒状骨材に硬化剤と粘結剤組成物を添加混練したものを
100℃以上に保持された金型に充填して加熱硬化し
て製造する際に用いられる高圧鋳造砂中子用粘結剤組成
物に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a composition for use in manufacturing sand cores to be applied to undercut portions in die casting for casting light alloys under high pressure. More specifically, several 10 kg/cm2 to several 100
A sand core applied to the undercut part in die casting for casting light alloys at a pressure of kg/cm2 is made by adding and kneading a hardening agent and a binder composition to refractory granular aggregate and keeping it at 100℃ or higher. The present invention relates to a binder composition for high-pressure casting sand cores, which is used when manufacturing sand cores by filling it into molds and curing with heat.
【0002】0002
【従来の技術及び発明が解決しようとする課題】従来、
中空製品あるいはアンダーカット製品を圧力鋳造で製造
する場合、製品を分割して鋳造した後、溶接その他の工
法で組み立てる方法で行われている。しかし、崩壊性砂
中子が使用できれば複雑な形状の製品の一体成型鋳造が
可能になり、鋳物品質の向上及びコスト・メリットが期
待できる。このような崩壊性砂中子の一部としては塩中
子が使用されているが、塩中子は複雑な形状の中子の成
型が難しく、更には、専用の金型及び成型機が必要であ
るためコスト高になり、省エネルギー、合理化のために
も代替する崩壊性砂中子が要求されている。砂中子成型
プロセスとしては、耐火性粒状骨材にフェノールノボラ
ック樹脂を被覆した、所謂レジンコーテッドサンドを成
型して熱硬化させるシェルモールド法が幅広く使用され
ている。このプロセスは設備的に簡便であり、作業的に
使用しやすい等の利点があるが、シェル砂中子は崩壊性
が悪く、バラシ工程で砂型を取り出すために熱処理を施
す必要があり、また、このプロセスは 250〜300
℃で焼成硬化させるのが通常で、それに起因して、鋳
型の歪み、変形による鋳物の寸法不良、作業環境等種々
の難点があり、これらの大幅な改善が望まれていた。[Prior art and problems to be solved by the invention] Conventionally,
When manufacturing hollow products or undercut products by pressure casting, the product is cast in parts and then assembled by welding or other construction methods. However, if a collapsible sand core can be used, it will be possible to integrally cast products with complex shapes, and improvements in casting quality and cost benefits can be expected. Salt cores are used as part of these collapsible sand cores, but salt cores are difficult to mold into cores with complex shapes, and furthermore, special molds and molding machines are required. Therefore, the cost is high, and a collapsible sand core is required as an alternative for energy saving and rationalization. As a sand core molding process, a shell molding method is widely used in which so-called resin-coated sand, in which fire-resistant granular aggregate is coated with a phenol novolac resin, is molded and thermally cured. This process has the advantage of being simple in terms of equipment and easy to use, but the shell sand core has poor collapsibility and requires heat treatment to take out the sand mold in the disassembly process. This process takes 250-300
It is common practice to bake and harden the castings at a temperature of 0.degree. C., which causes various problems such as distortion of the mold, poor dimensions of the casting due to deformation, and a working environment, and there has been a desire to significantly improve these problems.
【0003】そこで、これらの問題に対処するため、過
去数多くの研究がなされた。それらの中の1つとして、
特公昭61−29816 号公報が開示されたが、これ
は耐火性粒状骨材、酸硬化性樹脂、及び低級脂肪族スル
ホン酸又は芳香族スルホン酸と弱塩基との塩からなる触
媒の混合物を用いることにより、 150〜200 ℃
の低温で加熱硬化する所謂ウォームボックス法である。
これにより、温度による鋳型の歪み、変形による鋳物の
寸法精度や作業環境等が大幅に改善され、鋳鉄分野を中
心に広まっている。しかしながら、更に広範囲に適用で
きる造型システムとして、鋳型の物性向上、鋳物品質の
向上、作業環境等の改善が望まれている。[0003] In order to deal with these problems, many studies have been conducted in the past. As one of them,
Japanese Patent Publication No. 61-29816 has been disclosed, which uses a mixture of a refractory granular aggregate, an acid-curing resin, and a catalyst consisting of a salt of a lower aliphatic sulfonic acid or an aromatic sulfonic acid with a weak base. Possibly 150~200℃
This is the so-called warm box method, which heats and hardens at a low temperature. This has greatly improved the dimensional accuracy and work environment of castings due to temperature-induced distortion and deformation of the mold, and has become widespread mainly in the cast iron field. However, as a molding system that can be applied to a wider range of applications, improvements in the physical properties of molds, the quality of castings, and the working environment are desired.
【0004】0004
【課題を解決するための手段】本発明者らは、上記課題
を解決すべく鋭意研究の結果、本発明を完成するに到っ
たものである。即ち、数10kg/cm2 〜数100
kg/cm2 の圧力で軽合金を鋳造するダイカスト
においてアンダーカット部に適用される砂中子を耐火性
粒状骨材に硬化剤と粘結剤組成物を添加混練した後加熱
硬化して製造する際に用いられる粘結剤組成物であって
、フルフリルアルコール、フルフリルアルコール−ホル
マリン、尿素−ホルマリンの少なくとも1種の共縮合物
又は混合物を主成分とし、更に下記の(a) 〜(k)
から選ばれた熱可塑性樹脂の少なくとも1種:
(a) クマロン樹脂
(b) ケトン樹脂
(c) 酢酸ビニル樹脂
(d) ポリスチレン
(e) ポリビニルアルコール
(f) 石油樹脂
(g) ジシクロペンタジエン樹脂
(h) ロジン
(i) オルガノソルボリシス−リグニン(j) ビス
フェノールA残渣
(k) レゾルシン残渣
と、ホルマリン捕捉剤とを含有することを特徴とする高
圧鋳造砂中子用粘結剤組成物に係るものである。[Means for Solving the Problems] The present inventors have completed the present invention as a result of intensive research to solve the above problems. That is, several 10 kg/cm2 to several 100
When manufacturing a sand core applied to the undercut part in die casting for casting light alloys under a pressure of kg/cm2, the sand core is added to the fire-resistant granular aggregate and kneaded with a curing agent and a binder composition, then heated and hardened. A binder composition used in
At least one thermoplastic resin selected from: (a) Coumarone resin (b) Ketone resin (c) Vinyl acetate resin (d) Polystyrene (e) Polyvinyl alcohol (f) Petroleum resin (g) Dicyclopentadiene resin ( h) rosin (i) organosorvolysis-lignin (j) bisphenol A residue (k) resorcinol residue, and a formalin scavenger. be.
【0005】本発明の粘結剤組成物中の主成分としては
、フルフリルアルコール、フルフリルアルコール−ホル
マリン、尿素−ホルマリンの少なくとも1種の共縮合物
又は混合物が、鋳込み後の砂中子の崩壊性を更に改善す
るために使用され、それに併用される(a) 〜(k)
の熱可塑性樹脂の含有量は3〜30重量%が好ましい
。本発明の粘結剤組成物中の熱可塑性樹脂含有量が3重
量%未満では砂中子の初期強度を向上する効果が非常に
小さく、30重量%を越えると系の粘度が高くなり、混
練砂の流動性が悪く、砂中子強度が低下する。熱可塑性
樹脂の重量平均分子量としては、 300〜50,00
0のものが砂中子の初期強度を大幅に向上するので好ま
しい。重量平均分子量 300未満では初期強度を向上
させる効果が非常に小さく、50,000を越えると系
の粘度が高くなり、混練砂の流動性が悪く、砂中子強度
が低下する。[0005] The main component in the binder composition of the present invention is at least one co-condensate or mixture of furfuryl alcohol, furfuryl alcohol-formalin, and urea-formalin. (a) to (k) used to further improve disintegration properties and used in combination therewith
The content of the thermoplastic resin is preferably 3 to 30% by weight. If the thermoplastic resin content in the binder composition of the present invention is less than 3% by weight, the effect of improving the initial strength of the sand core will be very small, and if it exceeds 30% by weight, the viscosity of the system will increase and the kneading The fluidity of the sand is poor and the strength of the sand core is reduced. The weight average molecular weight of the thermoplastic resin is 300 to 50,00.
0 is preferable because it greatly improves the initial strength of the sand core. If the weight average molecular weight is less than 300, the effect of improving the initial strength will be very small, and if it exceeds 50,000, the viscosity of the system will increase, the fluidity of the kneaded sand will be poor, and the strength of the sand core will decrease.
【0006】本発明における粘結剤組成物中のホルマリ
ン捕捉剤の含有量は1.0 〜10.0重量%が好まし
い。含有量が 1.0重量%未満では砂中子を加熱硬化
して製造する際のホルマリン臭に起因する環境改善効果
が非常に小さく、10.0重量%を越えると、砂中子を
加熱硬化した後の樹脂の高分子量化が進まず、また架橋
密度も低下し、砂中子強度が低下する。ホルマリン捕捉
剤としては、尿素、フェノール、クレゾール、キシレノ
ール又はレゾルシンが好ましい。本発明における粘結剤
組成物は耐火性粒状骨材1000重量部に対して5〜5
0重量部の割合で使用するのが好ましい。5重量部未満
では充分な砂中子強度が得られず、50重量部を越える
と混練砂の流動性に悪影響を与える。本発明の粘結剤組
成物を用いて鋳型を製造する場合は、耐火性骨材と硬化
剤と共に混練して、100 ℃以上に保持された金型に
充填して、加熱硬化を行う。The content of formalin scavenger in the binder composition of the present invention is preferably 1.0 to 10.0% by weight. If the content is less than 1.0% by weight, the effect of improving the environment due to formalin odor during production by heating and hardening the sand core will be very small, and if it exceeds 10.0% by weight, the sand core will not be heated and hardened. After this, the polymerization of the resin does not progress, and the crosslinking density also decreases, resulting in a decrease in the strength of the sand core. Preferred formalin scavengers are urea, phenol, cresol, xylenol or resorcinol. The binder composition in the present invention is 5 to 5 parts by weight per 1000 parts by weight of the fire-resistant granular aggregate.
Preferably, it is used in a proportion of 0 parts by weight. If it is less than 5 parts by weight, sufficient sand core strength cannot be obtained, and if it exceeds 50 parts by weight, it will adversely affect the fluidity of the kneaded sand. When manufacturing a mold using the binder composition of the present invention, it is kneaded together with a refractory aggregate and a curing agent, filled into a mold kept at 100° C. or higher, and heat-cured.
【0007】本発明に使用される硬化剤組成物としては
弱塩基と低級脂肪族スルホン酸又は芳香族スルホン酸と
の塩を主成分とするものが使用され、通常耐火性粒状骨
材1000重量部に対して1〜30重量部の割合で使用
される。1重量部未満では充分な初期強度が得られず、
30重量部を越えると過度に硬化することになり、砂中
子の表面安定性が著しく低下する。一般に、硬化剤組成
物は粘結剤組成物100 重量部に対して15〜80重
量部の割合で使用するのが好ましい。尚、本発明におけ
る硬化剤組成物は通常、水や溶剤の溶液として使用され
る。この硬化剤組成物中に、澱粉、コーンスターチ、グ
ルコース、デキストリン等の糖類及びその誘導体等を含
有してもよい。The curing agent composition used in the present invention is one whose main component is a salt of a weak base and a lower aliphatic sulfonic acid or an aromatic sulfonic acid, and usually contains 1000 parts by weight of fire-resistant granular aggregate. It is used in a proportion of 1 to 30 parts by weight. If it is less than 1 part by weight, sufficient initial strength cannot be obtained,
If it exceeds 30 parts by weight, excessive hardening will result, and the surface stability of the sand core will be significantly reduced. Generally, it is preferable to use the curing agent composition in an amount of 15 to 80 parts by weight based on 100 parts by weight of the binder composition. Incidentally, the curing agent composition in the present invention is usually used as a solution of water or a solvent. This curing agent composition may contain saccharides such as starch, corn starch, glucose, dextrin, derivatives thereof, and the like.
【0008】酸硬化性樹脂に、鋳型強度や取り扱い易さ
を向上させるために、他の性能に悪影響を与えない範囲
内で希釈剤を混合しても差し支えない。その配合量は2
0重量%以下であることが好ましい。使用できる希釈剤
を具体的に例示すれば、ベンゼン、キシレン等の芳香族
炭化水素や、メタノール、エタノール、フルフリルアル
コール等のアルコール類や、ジエチルエーテル、アニソ
ール、アセタール等のエーテル類や、アセトン、メチル
エチルケトン等のケトン類や、テトラヒドロフラン、ジ
オキサン等の複素環炭化水素や、酢酸メチル、酢酸エチ
ル等のエステル類や、エチレングリコール、グリセリン
等の多価アルコール類や、2−メトキシエタノール、2
−エトキシエタノール等のセロソルブ類や、2−メトキ
シエチルアセテート、2−エトキシエチルアセテート、
2−ブトキシエチルアセテート、2−フェノキシエチル
アセテート等のセロソルブアセテート類や、ジエチレン
グリコールモノエチルエーテルアセテート等のカルビト
ールアセテート類等が挙げられる。更に、鋳型強度をよ
り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。シランカップリング剤としては、例えば、
γ−(2−アミノ)アミノプロピルメチルジメトキシシ
ラン、γ−アミノプロピルトリメトキシシラン、γ−ア
ミノプロピルトリエトキシシラン、γ−メルカプトプロ
ピルトリメトキシシラン、γ−グリシドキシプロピルト
リメトキシシラン等が挙げられる。本発明のシステムで
砂中子を製造する際の耐火性粒状骨材としては、石英質
を主成分とする珪砂の他、ジルコンサンド、クロマイト
サンド等が使用される。[0008] In order to improve mold strength and ease of handling, a diluent may be mixed with the acid-curable resin within a range that does not adversely affect other properties. Its blending amount is 2
It is preferably 0% by weight or less. Specific examples of diluents that can be used include aromatic hydrocarbons such as benzene and xylene, alcohols such as methanol, ethanol, and furfuryl alcohol, ethers such as diethyl ether, anisole, and acetal, acetone, Ketones such as methyl ethyl ketone, heterocyclic hydrocarbons such as tetrahydrofuran and dioxane, esters such as methyl acetate and ethyl acetate, polyhydric alcohols such as ethylene glycol and glycerin, 2-methoxyethanol, 2-methoxyethanol, etc.
- Cellosolves such as ethoxyethanol, 2-methoxyethyl acetate, 2-ethoxyethyl acetate,
Examples include cellosolve acetates such as 2-butoxyethyl acetate and 2-phenoxyethyl acetate, and carbitol acetates such as diethylene glycol monoethyl ether acetate. Furthermore, a silane coupling agent may be added for the purpose of further improving mold strength. As the silane coupling agent, for example,
Examples include γ-(2-amino)aminopropylmethyldimethoxysilane, γ-aminopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, γ-mercaptopropyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, etc. . As the refractory granular aggregate used to produce sand cores in the system of the present invention, silica sand containing quartz as a main component, zircon sand, chromite sand, etc. are used.
【0009】また、上記の様にして製造された砂中子は
、表面に従来一般に知られている表面被覆剤、即ちジル
コンフラワー、合成雲母、コロイダルシリカ等の耐火物
及び糖蜜、ヘントナイト等のバインダー成分を水、低級
アルコール等に混合して成る表面被覆剤を塗布・乾燥せ
しめて皮膜を形成した後に、金型内にセットし、数10
kg/cm2 〜数100 kg/cm2 の圧力で軽
合金をダイカスト機で鋳造する。[0009] Furthermore, the sand core produced as described above is coated with conventionally known surface coating agents, such as refractories such as zircon flour, synthetic mica, and colloidal silica, and binders such as molasses and hentonite. After coating and drying a surface coating agent made by mixing ingredients with water, lower alcohol, etc. to form a film, it is placed in a mold and
A light alloy is cast using a die-casting machine at a pressure of from kg/cm2 to several 100 kg/cm2.
【0010】0010
【実施例】以下本発明を実施例により詳細に説明するが
、本発明はこれらの実施例により制限されるものではな
い。
実施例1〜11及び比較例1〜6
オーストラリア産フラタリー硅砂1000重量部に対し
、硬化剤組成物(トルエンスルホン酸−銅塩:40重量
%、メタノール:40重量%、水:20重量%) 4.
5重量部、表1に示す粘結剤組成物15重量部を添加混
練した砂混合物をフランウォームボックス用垂直割造型
機に空気圧 4.0Kg/cm2にて吹き込み硬化温度
180℃で30秒間焼成し、砂の振出し性評価用砂中
子を成型した。シェルの砂中子はレジンコーテッドサン
ド(Resin Coated Sand,RCS)を
シェル用垂直割造型機に空気圧 1.5Kg/cm2に
て吹き込み、硬化温度 300℃で1分間焼成して成型
した。成型した砂中子にジルコンフラワー70重量部、
合成雲母20重量部、コロイダルシリカ10重量部、ヘ
ントナイト5重量部、糖蜜2重量部及び水40重量部よ
り成る表面被覆剤を塗布・乾燥せしめて皮膜を形成した
後に、金型内にセットし、 100kg/cm2 の圧
力でアルミニウム合金(材質AC−4C)をダイカスト
機で鋳造し砂の振出し性を評価した。その結果を表1及
び表2に示す。また、同様に25×25×250m/m
の曲げ強度測定用砂中子を硬化温度 180℃で20
秒間焼成し、焼成後15秒後の曲げ強度を測定した。そ
の結果を表1及び表2に示す。EXAMPLES The present invention will be explained in detail below with reference to Examples, but the present invention is not limited to these Examples. Examples 1 to 11 and Comparative Examples 1 to 6 Hardening agent composition (toluenesulfonic acid-copper salt: 40% by weight, methanol: 40% by weight, water: 20% by weight) based on 1000 parts by weight of Australian flattery silica sand 4 ..
A sand mixture prepared by adding and kneading 5 parts by weight and 15 parts by weight of the binder composition shown in Table 1 was blown into a vertically split molding machine for furan worm boxes at an air pressure of 4.0 kg/cm2 and baked at a hardening temperature of 180°C for 30 seconds. A sand core was molded for evaluation of sand shakeout performance. The sand core of the shell was molded by blowing resin coated sand (RCS) into a vertical molding machine for shells at an air pressure of 1.5 kg/cm 2 and baking at a hardening temperature of 300° C. for 1 minute. 70 parts by weight of zircon flour in the molded sand core.
A surface coating agent consisting of 20 parts by weight of synthetic mica, 10 parts by weight of colloidal silica, 5 parts by weight of hentonite, 2 parts by weight of molasses and 40 parts by weight of water was applied and dried to form a film, and then set in a mold, An aluminum alloy (material: AC-4C) was cast using a die-casting machine at a pressure of 100 kg/cm2, and the ability to shake out sand was evaluated. The results are shown in Tables 1 and 2. Similarly, 25 x 25 x 250 m/m
A sand core for measuring bending strength was cured at a temperature of 180°C for 20
It was fired for seconds, and the bending strength was measured 15 seconds after firing. The results are shown in Tables 1 and 2.
【0011】[0011]
【表1】[Table 1]
【0012】0012
【表2】[Table 2]
【0013】[0013]
【発明の効果】高圧で軽合金を鋳造するダイカストにお
いてアンダーカット部に適用される砂中子を製造する際
に、本発明の粘結剤組成物を用いることにより、鋳型の
物性向上と、鋳物品質の向上と、作業環境等の改善とが
可能となる。Effects of the Invention: By using the binder composition of the present invention when manufacturing sand cores that are applied to undercut parts in die casting for casting light alloys under high pressure, the physical properties of the mold can be improved and the castings can be improved. It is possible to improve quality and work environment.
Claims (4)
g/cm2 の圧力で軽合金を鋳造するダイカストにお
いてアンダーカット部に適用される砂中子を、耐火性粒
状骨材に硬化剤と粘結剤組成物を添加混練した後、加熱
硬化して製造する際に用いられる粘結剤組成物であって
、フルフリルアルコール、フルフリルアルコール−ホル
マリン、尿素−ホルマリンの少なくとも1種の共縮合物
又は混合物を主成分とし、更に下記の(a) 〜(k)
から選ばれた熱可塑性樹脂の少なくとも1種とホルマ
リン捕捉剤とを含有することを特徴とする高圧鋳造砂中
子用粘結剤組成物。 (a) クマロン樹脂 (b) ケトン樹脂 (c) 酢酸ビニル樹脂 (d) ポリスチレン (e) ポリビニルアルコール (f) 石油樹脂 (g) ジシクロペンタジエン樹脂 (h) ロジン (i) オルガノソルボリシス−リグニン(j) ビス
フェノールA残渣 (k) レゾルシン残渣[Claim 1] Several 10 kg/cm2 to several 100 k
A sand core that is applied to the undercut part in die casting for casting light alloys at a pressure of g/cm2 is manufactured by adding a curing agent and a binder composition to refractory granular aggregate, kneading it, and then heating and curing it. A binder composition used in the production of a binder containing at least one co-condensate or mixture of furfuryl alcohol, furfuryl alcohol-formalin, and urea-formalin as a main component, and further comprising the following (a) to ( k)
A binder composition for high-pressure casting sand cores, comprising at least one thermoplastic resin selected from the following and a formalin scavenger. (a) Coumarone resin (b) Ketone resin (c) Vinyl acetate resin (d) Polystyrene (e) Polyvinyl alcohol (f) Petroleum resin (g) Dicyclopentadiene resin (h) Rosin (i) Organosorvolysis-lignin (j ) Bisphenol A residue (k) Resorcinol residue
びホルマリン捕捉剤の含有率が、粘結剤組成物中各々3
〜30重量%及び1.0 〜10.0重量%である請求
項1記載の高圧鋳造砂中子用粘結剤組成物。2. The thermoplastic resin and formalin scavenger (a) to (k) each have a content of 3% in the binder composition.
30% by weight and 1.0 to 10.0% by weight of the binder composition for high-pressure casting sand cores according to claim 1.
〜50000 である請求項1記載の高圧鋳造砂中子用
粘結剤組成物。[Claim 3] The average molecular weight of the thermoplastic resin is 300.
50,000. The binder composition for high-pressure casting sand cores according to claim 1.
、クレゾール、キシレノール又はレゾルシンである請求
項1及び2記載の高圧鋳造砂中子用粘結剤組成物。4. The binder composition for high-pressure casting sand cores according to claims 1 and 2, wherein the formalin scavenger is urea, phenol, cresol, xylenol or resorcinol.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14873791A JPH04371343A (en) | 1991-06-20 | 1991-06-20 | Binder composition for sand core for high-pressure casting |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14873791A JPH04371343A (en) | 1991-06-20 | 1991-06-20 | Binder composition for sand core for high-pressure casting |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04371343A true JPH04371343A (en) | 1992-12-24 |
Family
ID=15459491
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14873791A Pending JPH04371343A (en) | 1991-06-20 | 1991-06-20 | Binder composition for sand core for high-pressure casting |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04371343A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006070247A (en) * | 2004-08-06 | 2006-03-16 | Kao Corp | Furan resin composition for casting mold manufacturing |
JP2012255129A (en) * | 2010-10-25 | 2012-12-27 | Sekisui Chem Co Ltd | Production method of furfuryl alcohol-formaldehyde copolymer |
JP2017519886A (en) * | 2014-06-27 | 2017-07-20 | テウォン ファーム カンパニー リミテッド | Method for producing spherical furan resin particles |
CN108299787A (en) * | 2018-01-12 | 2018-07-20 | 苏州兴业材料科技股份有限公司 | A kind of preparation method of the water soluble phenol resin composite material of casting |
-
1991
- 1991-06-20 JP JP14873791A patent/JPH04371343A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006070247A (en) * | 2004-08-06 | 2006-03-16 | Kao Corp | Furan resin composition for casting mold manufacturing |
US8124719B2 (en) | 2004-08-06 | 2012-02-28 | Kao Corporation | Furan resin composition for production of molds |
JP2012255129A (en) * | 2010-10-25 | 2012-12-27 | Sekisui Chem Co Ltd | Production method of furfuryl alcohol-formaldehyde copolymer |
JP2017519886A (en) * | 2014-06-27 | 2017-07-20 | テウォン ファーム カンパニー リミテッド | Method for producing spherical furan resin particles |
CN108299787A (en) * | 2018-01-12 | 2018-07-20 | 苏州兴业材料科技股份有限公司 | A kind of preparation method of the water soluble phenol resin composite material of casting |
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