JP2964371B2 - Release agent for mold casting - Google Patents
Release agent for mold castingInfo
- Publication number
- JP2964371B2 JP2964371B2 JP29630892A JP29630892A JP2964371B2 JP 2964371 B2 JP2964371 B2 JP 2964371B2 JP 29630892 A JP29630892 A JP 29630892A JP 29630892 A JP29630892 A JP 29630892A JP 2964371 B2 JP2964371 B2 JP 2964371B2
- Authority
- JP
- Japan
- Prior art keywords
- wax
- release agent
- silicate
- mold
- magnesium
- 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 - Fee Related
Links
- 238000005266 casting Methods 0.000 title claims description 20
- 239000001993 wax Substances 0.000 claims description 31
- -1 silicate compound Chemical class 0.000 claims description 29
- 239000003795 chemical substances by application Substances 0.000 claims description 23
- 239000002245 particle Substances 0.000 claims description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 claims description 8
- 239000000391 magnesium silicate Substances 0.000 claims description 8
- 229910052919 magnesium silicate Inorganic materials 0.000 claims description 8
- 235000019792 magnesium silicate Nutrition 0.000 claims description 8
- 239000007787 solid Substances 0.000 claims description 8
- 229910052582 BN Inorganic materials 0.000 claims description 7
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- 239000006082 mold release agent Substances 0.000 claims description 7
- 239000000725 suspension Substances 0.000 claims description 7
- 239000000454 talc Substances 0.000 claims description 7
- 229910052623 talc Inorganic materials 0.000 claims description 7
- 239000010439 graphite Substances 0.000 claims description 6
- 229910002804 graphite Inorganic materials 0.000 claims description 6
- 239000004698 Polyethylene Substances 0.000 claims description 5
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 claims description 5
- 229920000573 polyethylene Polymers 0.000 claims description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 4
- 239000002270 dispersing agent Substances 0.000 claims description 4
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 3
- 235000013871 bee wax Nutrition 0.000 claims description 3
- 239000012166 beeswax Substances 0.000 claims description 3
- SKKNACBBJGLYJD-UHFFFAOYSA-N bismuth magnesium Chemical compound [Mg].[Bi] SKKNACBBJGLYJD-UHFFFAOYSA-N 0.000 claims description 3
- 239000008119 colloidal silica Substances 0.000 claims description 3
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 claims description 3
- 229910052982 molybdenum disulfide Inorganic materials 0.000 claims description 3
- 239000012188 paraffin wax Substances 0.000 claims description 3
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims description 3
- 239000004810 polytetrafluoroethylene Substances 0.000 claims description 3
- 235000019353 potassium silicate Nutrition 0.000 claims description 3
- 239000004166 Lanolin Substances 0.000 claims description 2
- 240000007594 Oryza sativa Species 0.000 claims description 2
- 235000007164 Oryza sativa Nutrition 0.000 claims description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 2
- 239000000378 calcium silicate Substances 0.000 claims description 2
- 229910052918 calcium silicate Inorganic materials 0.000 claims description 2
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 claims description 2
- 239000004203 carnauba wax Substances 0.000 claims description 2
- 235000013869 carnauba wax Nutrition 0.000 claims description 2
- 229910052634 enstatite Inorganic materials 0.000 claims description 2
- 235000019388 lanolin Nutrition 0.000 claims description 2
- BBCCCLINBSELLX-UHFFFAOYSA-N magnesium;dihydroxy(oxo)silane Chemical compound [Mg+2].O[Si](O)=O BBCCCLINBSELLX-UHFFFAOYSA-N 0.000 claims description 2
- ZQKXQUJXLSSJCH-UHFFFAOYSA-N melamine cyanurate Chemical compound NC1=NC(N)=NC(N)=N1.O=C1NC(=O)NC(=O)N1 ZQKXQUJXLSSJCH-UHFFFAOYSA-N 0.000 claims description 2
- QLOAVXSYZAJECW-UHFFFAOYSA-N methane;molecular fluorine Chemical compound C.FF QLOAVXSYZAJECW-UHFFFAOYSA-N 0.000 claims description 2
- 239000010445 mica Substances 0.000 claims description 2
- 229910052618 mica group Inorganic materials 0.000 claims description 2
- 239000004200 microcrystalline wax Substances 0.000 claims description 2
- 235000019808 microcrystalline wax Nutrition 0.000 claims description 2
- 235000019809 paraffin wax Nutrition 0.000 claims description 2
- 235000019271 petrolatum Nutrition 0.000 claims description 2
- 235000009566 rice Nutrition 0.000 claims description 2
- 239000011435 rock Substances 0.000 claims description 2
- ITRNXVSDJBHYNJ-UHFFFAOYSA-N tungsten disulfide Chemical compound S=[W]=S ITRNXVSDJBHYNJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000002023 wood Substances 0.000 claims description 2
- FKHIFSZMMVMEQY-UHFFFAOYSA-N talc Chemical compound [Mg+2].[O-][Si]([O-])=O FKHIFSZMMVMEQY-UHFFFAOYSA-N 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 description 13
- 239000002184 metal Substances 0.000 description 13
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 238000009413 insulation Methods 0.000 description 7
- 239000011777 magnesium Substances 0.000 description 7
- 238000007711 solidification Methods 0.000 description 7
- 230000008023 solidification Effects 0.000 description 7
- 229910052749 magnesium Inorganic materials 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 230000007547 defect Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- PGZIKUPSQINGKT-UHFFFAOYSA-N dialuminum;dioxido(oxo)silane Chemical compound [Al+3].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O PGZIKUPSQINGKT-UHFFFAOYSA-N 0.000 description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 3
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical group [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 150000004760 silicates Chemical class 0.000 description 3
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000004512 die casting Methods 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000004705 High-molecular-weight polyethylene Substances 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- GANNOFFDYMSBSZ-UHFFFAOYSA-N [AlH3].[Mg] Chemical compound [AlH3].[Mg] GANNOFFDYMSBSZ-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 1
- 239000012164 animal wax Substances 0.000 description 1
- 150000001621 bismuth Chemical class 0.000 description 1
- 229940104825 bismuth aluminate Drugs 0.000 description 1
- 229940049676 bismuth hydroxide Drugs 0.000 description 1
- TZSXPYWRDWEXHG-UHFFFAOYSA-K bismuth;trihydroxide Chemical compound [OH-].[OH-].[OH-].[Bi+3] TZSXPYWRDWEXHG-UHFFFAOYSA-K 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000012669 compression test Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 150000002681 magnesium compounds Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005649 metathesis reaction Methods 0.000 description 1
- 239000012184 mineral wax Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000012165 plant wax Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
Landscapes
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Mold Materials And Core Materials (AREA)
Description
【0001】[0001]
【産業上の利用分野】この発明は、アルミニウムの金型
鋳造のうち、スクイズダイキャストなどのように、溶湯
を射出する速度が遅く、溶湯が冷え易い鋳造方法におい
て、かつ、長尺形状や大型で複雑な形状のものの鋳造な
どのように、離型性が厳しく要求される場合に好適に使
用することができる、断熱性(保温性)と離型性のよい
離型剤に関するものである。BACKGROUND OF THE INVENTION The present invention relates to a casting method in which the speed of injecting molten metal is low and the molten metal is easy to cool, such as squeeze die casting, among aluminum die castings. The present invention relates to a release agent having good heat insulating properties (heat retention properties) and good releasability, which can be suitably used in cases where mold release properties are strictly required, such as in casting of complicated shapes.
【0002】[0002]
【従来の技術】溶湯の射出速度が遅い(低速鋳込み)金
型鋳造法は、鋳造品へのガスの巻き込みがなく、高強度
の鋳造品を得ることができる。従って、このような鋳造
品は、自動車の軽量化指向に伴うアルミニウム部品の製
造に広く採用されている。従来、金型鋳造の際に用いら
れる離型剤は、黒鉛が主流であったが、黒色で周囲を汚
損するため、タルク、セリサイト、ろう石などの天然鉱
物、あるいは窒化硼素、PTFE(ポリテトラフルオロ
エチレン)等の白色離型剤が多く用いられている。これ
らの離型剤粒子は、カルボキシメチルセルロース(CM
C)等の分散剤を含む水中に懸濁させた塗料の形態で加
熱された鋳型に塗布し被膜を形成する。2. Description of the Related Art In a mold casting method in which a molten metal is injected at a low speed (low-speed casting), a high-strength cast product can be obtained without involving gas in the cast product. Therefore, such castings are widely used in the production of aluminum parts accompanying the trend toward reducing the weight of automobiles. Conventionally, graphite has been mainly used as a mold release agent at the time of mold casting. However, since it is black and stains the surroundings, natural minerals such as talc, sericite, and limestone, or boron nitride, PTFE (polyethylene) are used. White release agents such as tetrafluoroethylene) are often used. These release agent particles are made of carboxymethylcellulose (CM
The composition is applied to a heated mold in the form of a paint suspended in water containing a dispersant such as C) to form a film.
【0003】[0003]
【発明が解決しようとする課題】前記の金型鋳造法は、
金型内に溶湯を完全に充填する前に溶湯温度が下ると、
湯回りが悪くなり、湯じわ、湯境、あるいは欠肉などの
品質上の欠陥を起こし易いという欠点が潜在している。
さらに長尺形状や大型で複雑な形状の部品については、
凝固時の収縮により、離型性が悪くなり、製品に歪が生
じたり、製品が離型できなくなる場合もある。従来の離
型剤は熱伝導率が高いため、鋳造欠陥が比較的出難い単
純な形状の小形部品用としては好適であったが、大形で
複雑な形状あるいは薄肉の部品の場合には、湯回り不良
による品質欠陥が発生し易いという問題点があった。こ
の発明は、以上のような事情に鑑み、溶湯が冷え難いと
いう効果を示す断熱性(保温性)を有し、低速鋳込み鋳
造法において品質欠陥を起こすことなく、かつ大型部品
においても良好な離型性を示す離型剤を提供することを
目的とするものである。SUMMARY OF THE INVENTION
If the temperature of the molten metal drops before the molten metal is completely filled in the mold,
There is a potential drawback that the running of the hot water deteriorates and quality defects such as hot water lines, hot water borders, and underfill are easily caused.
For parts with long shapes or large and complicated shapes,
Due to shrinkage during solidification, the releasability deteriorates, and the product may be distorted or the product may not be released. Conventional release agents have high thermal conductivity and are suitable for small parts with simple shapes where casting defects are relatively difficult to appear.However, in the case of large and complicated shapes or thin parts, There is a problem that quality defects due to poor running of the molten metal easily occur. In view of the circumstances described above, the present invention has a heat insulating property (heat retention property) that has an effect that a molten metal is hardly cooled, does not cause a quality defect in a low-speed casting method, and has a good separation even in a large part. It is an object of the present invention to provide a release agent having moldability.
【0004】[0004]
【課題を解決するための手段】上記の課題を解決するた
めに、この発明の金型鋳造用離型剤は、分散剤を含む水
中に懸濁させる離型剤粒子として、ワックスと多孔質で
比表面積が40m2/g以上の合成珪酸化合物粒子とを用
いることを特徴とするものである。この場合に、ワック
スは、木ろう、蜜ろう、ライスワックス、カルナバワッ
クス、羊毛ろう、パラフィンワックス、マイクロクリス
タリンワックスおよびポリエチレンワックスの少なくと
も1種であり、合成珪酸化合物は、珪酸アルミン酸マグ
ネシウム、メタ珪酸アルミン酸マグネシウム、珪酸アル
ミニウム、珪酸マグネシウム、珪酸アルミン酸マグネシ
ウムビスマスおよび珪酸カルシウムの少なくとも1種で
あることを特徴としている。また、前記ワックスおよび
合成珪酸化合物からなる離型剤粒子の他に、固形分とし
て90重量%未満のタルク、セリサイト、ろう石、窒化
硼素、二硫化モリブデン、二硫化タングステン、マイ
カ、エンスタタイト、炭酸カルシウム、弗化黒鉛、PT
FE、メラミンシアヌレートおよび黒鉛のうち少なくと
も1種を含有することを特徴とする。更に、これらの離
型剤懸濁液中に、水ガラスまたはコロイド状シリカを含
有することを特徴とするものである。SUMMARY OF THE INVENTION In order to solve the above problems, a mold release agent for mold casting according to the present invention comprises a wax and a porous material as release agent particles suspended in water containing a dispersant. It is characterized by using synthetic silicate compound particles having a specific surface area of 40 m 2 / g or more. In this case, the wax is at least one of wood wax, beeswax, rice wax, carnauba wax, wool wax, paraffin wax, microcrystalline wax and polyethylene wax, and the synthetic silicate compound is magnesium aluminate silicate, metasilicate It is characterized in that it is at least one of magnesium aluminate, aluminum silicate, magnesium silicate, magnesium bismuth silicate and calcium silicate. Further, in addition to the wax and the release agent particles composed of the synthetic silicate compound, talc, sericite, rock, boron nitride, molybdenum disulfide, tungsten disulfide, mica, enstatite having a solid content of less than 90% by weight, Calcium carbonate, fluorinated graphite, PT
It is characterized by containing at least one of FE, melamine cyanurate and graphite. Further, the release agent suspension is characterized by containing water glass or colloidal silica.
【0005】上記ワックスには、化粧品に用いられる蜜
ろう等の動・植物ろう、食品包装に用いられるパラフィ
ンワックス等の鉱物性ワックスおよびポリエチレンワッ
クス等の合成ワックスがある。合成ワックスのうち、例
えばポリエチレンワックスはエチレンの高圧重合、低圧
(チーグラー型触媒)重合、または高分子量ポリエチレ
ンの熱分解によって製造される。前記の8種類のワック
スは、現在比較的入手し易い物質であるが、これらと類
似する各種の誘導体も作用および効果は同様であると推
察される。The above waxes include animal and plant waxes such as beeswax used for cosmetics, mineral waxes such as paraffin wax used for food packaging, and synthetic waxes such as polyethylene wax. Among the synthetic waxes, for example, polyethylene wax is produced by high-pressure polymerization of ethylene, low-pressure (Ziegler-type catalyst) polymerization, or thermal decomposition of high-molecular-weight polyethylene. The above-mentioned eight types of waxes are relatively easily available at present, but it is presumed that various derivatives similar to these have similar functions and effects.
【0006】また、上記合成珪酸化合物は、医薬品の酸
吸着剤として用いられているものと同様に、化学的に合
成される化合物であり、多孔質で、比表面積は40m2/
g以上で、粒度は0.01〜30μm程度である。この
合成珪酸化合物は、例えば珪酸アルミン酸マグネシウム
の場合、珪酸ソーダ、アルミン酸ソーダおよび塩化マグ
ネシウムの複分解により得られる。また、珪酸アルミン
酸マグネシウムビスマスの場合には、アルミニウム塩の
水溶液に炭酸マグネシウム等の塩基性マグネシウム化合
物の希薄溶液を加えて塩基性アルミニウム塩を沈澱さ
せ、これにビスマス塩の酸性水溶液を加えて反応させ、
塩基性アルミニウムマグネシウム塩と水酸化ビスマスと
を結合させて調製することができる。また、前記の6種
類の合成珪酸化合物は、現在入手し易い物質であるが、
これらと類似する各種の誘導体も作用および効果は同様
であると推察される。[0006] The above-mentioned synthetic silicate compound is a compound that is chemically synthesized similarly to the one used as an acid adsorbent for pharmaceuticals, and is porous and has a specific surface area of 40 m 2 / m 2 .
g or more, the particle size is about 0.01 to 30 μm. For example, in the case of magnesium silicate, this synthetic silicate compound is obtained by metathesis of sodium silicate, sodium aluminate and magnesium chloride. In the case of magnesium bismuth aluminate silicate, a basic aluminum salt is precipitated by adding a dilute solution of a basic magnesium compound such as magnesium carbonate to an aqueous solution of an aluminum salt, and an acidic aqueous solution of a bismuth salt is added thereto for reaction. Let
It can be prepared by combining a basic aluminum magnesium salt with bismuth hydroxide. Further, the above-mentioned six types of synthetic silicate compounds are substances that are easily available at present,
It is presumed that various derivatives similar to these have similar actions and effects.
【0007】前記の多孔質とは、粒子表面部または粒子
全体が多孔質であるもの、および微細な一次粒子が約1
μm前後の凝集粒子を形成して多孔質状になっているも
のを包含する。断熱性試験を行った結果によれば、比表
面積が40m2/gより小さい合成珪酸化合物は断熱性が
劣っている。また、比表面積の大きいものとしては、工
業上は400m2/g程度のものがあり、これも勿論使用
できる。[0007] The above-mentioned porous material means that the surface of the particle or the whole particle is porous, and that the fine primary particles are about 1%.
Includes those that are formed into porous particles by forming aggregated particles of about μm. According to the result of the heat insulation test, the synthetic silicate compound having a specific surface area of less than 40 m 2 / g is inferior in heat insulation. In addition, a material having a large specific surface area is industrially about 400 m 2 / g, which can be used as a matter of course.
【0008】この発明の離型剤のうち、ワックスおよび
珪酸化合物粒子からなる離型剤は、金型への被膜形成性
が比較的弱いが、潤滑性および断熱性が良いため、鋳造
品が単純な形状のものから凝固時の収縮率の大きい長尺
形状のものまで広範囲に適している。鋳造品が複雑な形
状の場合には、ワックスおよび珪酸化合物粒子のみの離
型剤よりも、前記のタルク、セリサイト、窒化硼素、弗
化黒鉛などの固体潤滑剤粒子を添加して、潤滑性を維持
しつつ、金型への被膜形成性を向上させたものが適して
いる。この場合、合成珪酸化合物粒子の量は固形分とし
て10重量%以上である。合成珪酸化合物粒子の量がこ
れより少ないと断熱性があまり向上しない。またワック
スの量は、固形分として0.1〜20重量%が好まし
い。0.1重量%未満では潤滑性の向上にあまり効果が
なく、20重量%を超えるとガス発生量が多くなり、鋳
造品内部へのガスの巻き込みによる鋳造欠陥が生じ易く
なる。また、上記の固体潤滑剤粒子のうち黒鉛と二硫化
モリブデンは黒灰色であるから、用いる場合は少量にす
ることが好ましい。[0008] Among the release agents of the present invention, the release agent composed of wax and silicate compound particles has relatively poor film-forming properties on a mold, but has good lubricity and heat insulation properties, so that a cast product is simple. It is suitable for a wide range of products from various shapes to long shapes having a large shrinkage rate during solidification. When the casting has a complicated shape, solid lubricant particles such as talc, sericite, boron nitride, graphite fluoride, etc. are added rather than a release agent consisting of only wax and silicate compound particles to improve lubricity. It is suitable that the film forming property on the mold is improved while maintaining the above. In this case, the amount of the synthetic silicate compound particles is 10% by weight or more as a solid content. If the amount of the synthetic silicate compound particles is less than this, the heat insulating properties are not significantly improved. The amount of the wax is preferably 0.1 to 20% by weight as a solid content. If the amount is less than 0.1% by weight, the lubricating property is not significantly improved. If the amount exceeds 20% by weight, the amount of generated gas increases, and casting defects due to entrainment of gas into the casting are liable to occur. In addition, among the solid lubricant particles, graphite and molybdenum disulfide are black-gray, so that when they are used, it is preferable to use a small amount.
【0009】鋳物品の形状や寸法によって、金型面への
離型剤塗膜の接着性が必要な場合には、懸濁液中に水ガ
ラスまたはコロイド状シリカを添加することができる。
その量は固形分として約2〜15重量%程度が好まし
い。When adhesion of the release agent coating to the mold surface is required depending on the shape and size of the cast article, water glass or colloidal silica can be added to the suspension.
The amount is preferably about 2 to 15% by weight as a solid content.
【0010】なお、この発明に係る離型剤懸濁液は、調
合時には固形分の濃度を高くしておき、通常、使用時に
金型の寸法、形状、塗布条件に合わせて適宜の濃度に水
で希釈して用いる。The release agent suspension according to the present invention has a high solid content at the time of preparation, and usually has an appropriate concentration of water at the time of use according to the size, shape and application conditions of the mold. Dilute with and use.
【0011】[0011]
【作用】従来から用いられているタルク等の天然鉱物や
窒化硼素などは、結晶性の単一粒子からなり、粒子自体
は熱伝導性がよい。このような材料の離型剤を金型面に
塗布し被膜を形成して溶湯を注ぎ込むと、溶湯の熱は容
易に金型に伝わり放熱されるから、溶湯温度の低下が著
しく、湯流れが悪化する。合成珪酸化合物は、多孔質粒
子であるから、塗膜を形成した場合に、塗膜中に細かに
分散した空隙により優れた断熱性を示し、これによって
溶湯の冷えを抑制するため、湯回り性が向上する。これ
にワックスを加えると、合成珪酸化合物の間に入り込ん
だワックスが、鋳造時に液状でまたは蒸発して合成珪酸
化合物粒子同士の流動性を向上させ、実質的に潤滑性お
よび離型性の良好な離型剤となる。また、合成珪酸化合
物およびワックスは、白色または淡黄色の物質であるか
ら作業環境を悪化させない。The natural minerals such as talc and boron nitride which are conventionally used are composed of single crystalline particles, and the particles themselves have good thermal conductivity. When a mold release agent made of such a material is applied to the mold surface to form a coating and the molten metal is poured, the heat of the molten metal is easily transmitted to the mold and radiated. Getting worse. Since the synthetic silicate compound is a porous particle, when a coating film is formed, it exhibits excellent heat insulating properties due to finely dispersed voids in the coating film, thereby suppressing cooling of the molten metal. Is improved. When wax is added to the wax, the wax that has entered between the synthetic silicate compounds is liquid or evaporates during casting to improve the fluidity between the synthetic silicate compound particles, and has substantially good lubricity and releasability. It becomes a release agent. Further, since the synthetic silicate compound and the wax are white or pale yellow substances, they do not deteriorate the working environment.
【0012】[0012]
【実施例】以下、実施例により説明する。分散剤として
2重量%のCMCを水に溶解した液に、各種の無機粉体
20重量%を、凝集塊が生じないように徐々に添加し、
十分に撹拌して無機粉体懸濁液を調製した。次に10重
量%の乳化剤(ポリオキシエチレンアルキルエーテル)
に20重量%の各種ワックスを加え、よく撹拌した。こ
れに70重量%の水を徐々に加え、ホモジナイザーによ
り十分に撹拌し分散させてワックス乳化液を調製した。
上記2液を必要な比率で混合し撹拌して試料とした。表
1に無機粉体の種類とそれぞれの比表面積を示す。表1
のタルク、セリサイト、窒化硼素および黒鉛は、従来の
離型剤に含まれている無機粉体であり、一方珪酸アルミ
ン酸マグネシウム、珪酸アルミニウムおよび珪酸マグネ
シウムはこの発明に係る合成珪酸化合物である。また、
表2および表3に、無機粉体およびワックスの全量を1
00重量%とする各材料の配合量と、離型剤を塗布した
被膜の断熱性および摩擦係数を試験した結果とを示す。
なお、表2および表3において、材料欄の「珪酸Al・M
g」、「珪酸Al」および「珪酸Mg」はそれぞれ表1の
E、F、Gすなわち、合成珪酸アルミン酸マグネシウ
ム、合成珪酸アルミニウムおよび合成珪酸マグネシウム
を示す。Embodiments will be described below with reference to embodiments. To a liquid in which 2% by weight of CMC was dissolved in water as a dispersant, 20% by weight of various inorganic powders were gradually added so as not to cause agglomerates,
The mixture was sufficiently stirred to prepare an inorganic powder suspension. Next, 10% by weight of an emulsifier (polyoxyethylene alkyl ether)
Was added with 20% by weight of various waxes, followed by thorough stirring. 70% by weight of water was gradually added thereto, and the mixture was sufficiently stirred and dispersed by a homogenizer to prepare a wax emulsion.
The two liquids were mixed at a required ratio and stirred to obtain a sample. Table 1 shows the types of the inorganic powders and the respective specific surface areas. Table 1
Talc, sericite, boron nitride and graphite are inorganic powders contained in conventional mold release agents, while magnesium silicate, aluminum silicate and magnesium silicate are synthetic silicate compounds according to the present invention. Also,
Tables 2 and 3 show that the total amount of inorganic powder and wax is 1
The amounts of the respective materials to be set to 00% by weight and the results of tests on the heat insulating properties and the coefficient of friction of the coating applied with the release agent are shown.
In Tables 2 and 3, "Material Silicate Al
“g”, “Al silicate” and “Mg silicate” represent E, F, and G in Table 1, that is, synthetic magnesium aluminate, synthetic aluminum silicate, and synthetic magnesium silicate, respectively.
【0013】[0013]
【表1】 [Table 1]
【0014】[0014]
【表2】 [Table 2]
【0015】[0015]
【表3】 [Table 3]
【0016】離型剤被膜の断熱性は、下記の方法による
溶湯の凝固時間で評価した。金型は、20mm×200
mmで深さ200mmのキャビティを有し、厚さは20
mmである。また、上方に湯口と、キャビティ中央の温
度を測定する熱電対とを備え、縦割りに二分割されてボ
ルトで組み立てられる構造を有している。この金型を分
解して約150℃に加熱し、前記各懸濁液試料を水で1
0倍に希釈したものを金型内面に噴霧して、厚さ約5μ
mの塗膜を形成し、金型を組み立てた後、240℃に昇
温して、温度720℃のアルミニウム(AC4C)の溶
湯を注入し、凝固までの時間を測定した。The heat insulating property of the release agent film was evaluated by the solidification time of the molten metal according to the following method. The mold is 20mm x 200
mm cavity with a depth of 200 mm and a thickness of 20 mm
mm. Further, a gate and a thermocouple for measuring the temperature at the center of the cavity are provided at the upper part, and the structure is divided vertically into two parts and assembled by bolts. The mold was disassembled and heated to about 150 ° C., and each of the suspension samples was diluted with water for 1 hour.
Spray the solution diluted 0-fold onto the inner surface of the mold to obtain a thickness of about 5μ.
After forming a coating film of m and assembling a mold, the temperature was raised to 240 ° C., a molten aluminum (AC4C) at a temperature of 720 ° C. was poured, and the time until solidification was measured.
【0017】離型剤被膜の潤滑性は、リング圧縮試験法
により求めた摩擦係数で評価した。金型は、直径60m
m、高さ50mmを有し、材質はSKD61であり、こ
れを2個用いる。この金型を約160℃に加熱し、前記
各懸濁液試料を水で10倍に希釈したものを金型面に噴
霧して、厚さ約5μmの塗膜を均一に形成させた。その
後400℃に加熱した試験片(材質AC4C、外径20
mm、内径10mm、高さ5mm)を2つの金型の塗膜
形成面ではさみ、アムスラー型試験機により圧縮率40
%で圧縮した。試験片の圧縮率と内径変化率より摩擦係
数を算出した。The lubricity of the release agent film was evaluated based on the coefficient of friction obtained by the ring compression test method. The mold is 60m in diameter
m, height 50 mm, the material is SKD61, and two of them are used. The mold was heated to about 160 ° C., and each suspension sample diluted 10-fold with water was sprayed on the mold surface to uniformly form a coating film having a thickness of about 5 μm. Thereafter, the test piece (material AC4C, outer diameter 20) heated to 400 ° C.
mm, inner diameter 10 mm, height 5 mm) between the coating surfaces of the two molds, and a compression ratio of 40 using an Amsler type testing machine.
% Compressed. The friction coefficient was calculated from the compressibility and the change in inner diameter of the test piece.
【0018】表2に示すように、窒化硼素、タルク、セ
リサイトおよび黒鉛のみの試料1〜4は、凝固時間が1
20秒以下であり、断熱効果が低い。珪酸アルミン酸マ
グネシウム、珪酸アルミニウム、珪酸マグネシウムの多
孔質粒子を用いた試料5〜7は、凝固時間が190秒前
後を示しており、断熱効果が優れているが、摩擦係数は
0.40以上の高い値を示し、潤滑性の点でやや劣るこ
とが判る。これに比し、合成珪酸化合物とワックスを組
み合わせた本発明の試料9〜14は、凝固時間が180
〜191秒と良好な断熱性を示し、 摩擦係数は0.03
〜0.10と低く潤滑性も良好であることが判る。ま
た、本発明の成分に従来の無機粉体を加えた試料15〜
20においても、断熱効果と潤滑性が共に良好な値を示
していることが判る。珪酸アルミン酸マグネシウムおよ
びワックスの混合割合と断熱性および摩擦係数との関係
は、試料5、9、10および11の比較により知ること
ができる。すなわち、珪酸アルミン酸マグネシウムのみ
の試料5は断熱性が最も良いが、摩擦係数は高く潤滑性
は良くない。これにワックスを5、10および15重量
%(それぞれ試料9、10および11)と添加すること
により、断熱効果を大きく阻害することなく、摩擦係数
が大幅に低下し、潤滑性が向上していることが判る。As shown in Table 2, Samples 1-4 containing only boron nitride, talc, sericite and graphite had a solidification time of 1
20 seconds or less, the heat insulation effect is low. Samples 5 to 7 using porous particles of magnesium aluminate, aluminum silicate, and magnesium silicate show a solidification time of about 190 seconds and have an excellent heat insulating effect, but have a friction coefficient of 0.40 or more. It shows a high value, indicating that the lubricity is slightly inferior. In contrast, Samples 9 to 14 of the present invention, in which a synthetic silicate compound and a wax were combined, had a solidification time of 180
It shows good heat insulation of ~ 191 seconds, and friction coefficient is 0.03
It can be seen that the lubricating property is good, being as low as about 0.10. Samples 15 to 15 obtained by adding a conventional inorganic powder to the components of the present invention
20 also shows that both the heat insulation effect and the lubricity show good values. The relationship between the mixing ratio of magnesium aluminate silicate and wax and the heat insulating properties and the coefficient of friction can be found by comparing Samples 5, 9, 10 and 11. That is, the sample 5 containing only magnesium aluminate silicate has the best heat insulating property, but has a high friction coefficient and poor lubricity. By adding the wax to 5, 10 and 15% by weight (samples 9, 10 and 11, respectively), the friction coefficient is greatly reduced and the lubricity is improved without greatly impairing the heat insulating effect. You can see that.
【0019】[0019]
【発明の効果】以上説明したように、本発明の離型剤は
断熱性と潤滑性に優れているため、金型内に充填される
アルミニウム溶湯の冷却速度を遅らせることができるの
で、低速射出鋳造に適用すれば、湯回り、湯流れ性が良
くなり、しかも摩擦係数を低減することができるので離
型性が著しく向上する。以上のような効果により、複雑
な形状の高品質のアルミ鋳物を生産することが可能とな
る。As described above, the release agent of the present invention is excellent in heat insulation and lubricity, so that the cooling rate of the aluminum melt filled in the mold can be slowed, so that low-speed injection can be achieved. If the present invention is applied to casting, the flow of the molten metal and the flowability of the molten metal are improved, and the coefficient of friction can be reduced. With the above effects, it is possible to produce a high-quality aluminum casting having a complicated shape.
Claims (5)
上の多孔質合成珪酸化合物からなる離型剤粒子を、分散
剤を含有する水に懸濁させたことを特徴とする金型鋳造
用離型剤。1. A mold casting mold release agent characterized in that wax and a release agent particle comprising a porous synthetic silicate compound having a specific surface area of 40 m 2 / g or more are suspended in water containing a dispersant. Mold.
スワックス、カルナバワックス、羊毛ろう、パラフィン
ワックス、マイクロクリスタリンワックスおよびポリエ
チレンワックスの少なくとも1種であることを特徴とす
る請求項1に記載の金型鋳造用離型剤。2. The wax according to claim 1, wherein the wax is at least one of wood wax, beeswax, rice wax, carnauba wax, wool wax, paraffin wax, microcrystalline wax and polyethylene wax. Release agent for mold casting.
マグネシウム、メタ珪酸アルミン酸マグネシウム、珪酸
アルミニウム、珪酸マグネシウム、珪酸アルミン酸マグ
ネシウムビスマスおよび珪酸カルシウムの少なくとも1
種であることを特徴とする請求項1または2に記載の金
型鋳造用離型剤。3. The synthetic silicate compound comprises at least one of magnesium silicate, magnesium metasilicate, magnesium silicate, aluminum silicate, magnesium silicate, magnesium bismuth silicate and calcium silicate.
The mold release agent for mold casting according to claim 1 or 2, which is a seed.
量%未満のタルク、セリサイト、ろう石、窒化硼素、二
硫化モリブデン、二硫化タングステン、マイカ、エンス
タタイト、炭酸カルシウム、弗化黒鉛、PTFE、メラ
ミンシアヌレートおよび黒鉛のうち少なくとも1種を含
有することを特徴とする請求項1から3のいずれかに記
載の金型鋳造用離型剤。4. The release agent particles wherein the solid content is less than 90% by weight of talc, sericite, rock, boron nitride, molybdenum disulfide, tungsten disulfide, mica, enstatite, calcium carbonate, graphite fluoride. The mold release agent according to any one of claims 1 to 3, comprising at least one of PTFE, PTFE, melamine cyanurate and graphite.
またはコロイド状シリカを含有することを特徴とする請
求項1から4のいずれかに記載の金型鋳造用離型剤。5. The release agent for mold casting according to claim 1, wherein the suspension of the release agent particles contains water glass or colloidal silica.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP29630892A JP2964371B2 (en) | 1992-10-07 | 1992-10-07 | Release agent for mold casting |
| US08/084,172 US5409531A (en) | 1992-07-01 | 1993-07-01 | Releasing agent for die casting |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP29630892A JP2964371B2 (en) | 1992-10-07 | 1992-10-07 | Release agent for mold casting |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH06114494A JPH06114494A (en) | 1994-04-26 |
| JP2964371B2 true JP2964371B2 (en) | 1999-10-18 |
Family
ID=17831870
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP29630892A Expired - Fee Related JP2964371B2 (en) | 1992-07-01 | 1992-10-07 | Release agent for mold casting |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2964371B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3866896B2 (en) | 2000-03-17 | 2007-01-10 | 日華化学株式会社 | Aqueous mold release agent for low speed injection mold casting. |
-
1992
- 1992-10-07 JP JP29630892A patent/JP2964371B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH06114494A (en) | 1994-04-26 |
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