JPS60166140A - Thermal expandability imparting agent for embedding material - Google Patents

Thermal expandability imparting agent for embedding material

Info

Publication number
JPS60166140A
JPS60166140A JP59022498A JP2249884A JPS60166140A JP S60166140 A JPS60166140 A JP S60166140A JP 59022498 A JP59022498 A JP 59022498A JP 2249884 A JP2249884 A JP 2249884A JP S60166140 A JPS60166140 A JP S60166140A
Authority
JP
Japan
Prior art keywords
imparting agent
embedding material
expandability
thermal expansion
calcia
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
Application number
JP59022498A
Other languages
Japanese (ja)
Other versions
JPH0155063B2 (en
Inventor
Fuminobu Kubo
久保 文信
Kazuyoshi Fujiwara
藤原 和能
Kazuhiko Kamiara
上新 和彦
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
TAISEI SHIKA KOGYO KK
Original Assignee
TAISEI SHIKA KOGYO KK
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by TAISEI SHIKA KOGYO KK filed Critical TAISEI SHIKA KOGYO KK
Priority to JP59022498A priority Critical patent/JPS60166140A/en
Publication of JPS60166140A publication Critical patent/JPS60166140A/en
Publication of JPH0155063B2 publication Critical patent/JPH0155063B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22CFOUNDRY MOULDING
    • B22C1/00Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
    • B22C1/02Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by additives for special purposes, e.g. indicators, breakdown additives
    • B22C1/08Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by additives for special purposes, e.g. indicators, breakdown additives for decreasing shrinkage of the mould, e.g. for investment casting

Abstract

PURPOSE:To compensate shrinkage of an alloy during casting only by the thermal expansion concerning precision casting of a dental casting by adding a thermal expandability imparting agent consisting of molten calcium or calcia clinker to an embedding material. CONSTITUTION:A thermal expandability imparting agent consisting of molten calcium or calcia clinker is added to, for example, a phosphate embedding material. The embedding material mixed with such imparting agent is kneaded by water or colloidal silica soln. and is packed in a ring, then the material is heated by the conventional method. The embedding material has a high rate of thermal expansion with substantially no expansion on hardening. The shrinkage of the alloy during casting is thus compensated by only the thermal expansion.

Description

【発明の詳細な説明】 (産業上の利用分野) この発明は、歯科用鋳造品の精密鋳造に使用する埋没材
に混合して埋没材の加熱膨張性を向上させるための加熱
膨張性イ1与剤である。
Detailed Description of the Invention (Field of Industrial Application) The present invention provides a heat-expandable material 1 for improving the heat-expandability of the investment material by mixing it with the investment material used for precision casting of dental castings. It is a drug.

(従来技術) 金属冠やインレーなどの歯科用鋳造品の精密鋳造におい
て、埋没材の成型空所に注入された合金の溶湯が冷却固
化される際に、合金が約1.4〜2.3%収縮するため
に上記成型空所をあらかじめ膨張させておく必要があり
、この膨張は埋没材の硬化時および加熱時に生ずる膨張
によって行なわれている。しかしながら硬化膨張の大き
い埋没材を使用すると鋳造体が変形するので、合金の収
縮の補償は埋没材の加熱膨張のみを利用すべきであるこ
とが要望されている。
(Prior art) In precision casting of dental castings such as metal crowns and inlays, when the molten alloy injected into the molding cavity of the investment material is cooled and solidified, the alloy becomes approximately 1.4 to 2.3 % shrinkage, it is necessary to expand the molding cavity beforehand, and this expansion is carried out by the expansion that occurs during curing and heating of the investment material. However, if an investment material with a large hardening expansion is used, the cast body will be deformed, so it is desired that only the heating expansion of the investment material be used to compensate for the shrinkage of the alloy.

シリカなどの耐火材に、第1リン酸アンモニウムおよび
酸化マグネシウムを結合材として混合したリン酸塩系埋
没材は、耐熱性が大きく、鋳造時の強度が大きいので、
ニッケル・クロム合金、コバルト・クロム合金などの比
較的融点の高い合金の鋳造に広く使用されているが、こ
の埋没材の加熱膨張率は1%程度であって、加熱膨張の
みで合金の収縮を十分に補償することはできない、リン
酸塩系埋没材の加熱膨張率の向上について種々の研究が
されているが、硬化膨張がほとんどなくて加熱膨張のみ
が大きい埋没材は未だ知られていなし)。
Phosphate-based investment materials, which are made by mixing refractory materials such as silica with monoammonium phosphate and magnesium oxide as binders, have high heat resistance and high strength when cast.
It is widely used for casting alloys with relatively high melting points, such as nickel-chromium alloys and cobalt-chromium alloys, but the thermal expansion coefficient of this investment material is about 1%, so heating expansion alone does not cause the alloy to shrink. Although various studies have been conducted on improving the coefficient of thermal expansion of phosphate-based investment materials, which cannot fully compensate, there is still no known investment material that exhibits almost no curing expansion and only large thermal expansion.) .

一方、カルシア(酸化カルシウムCab)を高温にて加
熱して溶融し、溶融状態で細粒化し、急速に凝固させた
溶融カルシアは、溶鋼の精練剤、もしくは耐火材料とし
て使用されている。またカルシアにMn0g、Ti1t
、 Fe20g、 Cr20B、CaFz、^IFgな
どの化合物の1種または2種以上を添加し、この混合物
を1200〜1600℃で焼結し、冷却後粉砕したカル
シアクリンカ−は、耐消化性が優れたものとしてや金柑
に広く使用されている。しかしながら溶融カルシアおよ
びカルシアクリンカ−を埋没材の加熱膨張性付与剤とし
て使用することは未だ知られていなかった。
On the other hand, molten calcia, which is obtained by heating and melting calcia (calcium oxide Cab) at a high temperature, making the particles fine in the molten state, and solidifying them rapidly, is used as a refining agent for molten steel or as a refractory material. Also, Calcia has 0g of Mn and 1t of Ti.
, Fe20g, Cr20B, CaFz, ^IFg, and other compounds are added to the calcia clinker, which is sintered at 1200-1600℃, cooled, and then crushed. Calcia clinker has excellent digestion resistance. It is widely used as a vegetable and for kumquats. However, it has not yet been known to use molten calcia and calcia clinker as a thermal expansion agent for investment materials.

(発明の目的) この発明は、上記溶融カルシアまたはカルシアクリンカ
−を埋没材に添加することによって、埋没材の硬化膨張
がほとんどなく加熱膨張が大きくなる加熱膨張性付与剤
を提供することを目的とするものである。
(Object of the invention) An object of the present invention is to provide a heat-expandability imparting agent that causes almost no curing expansion of the investment material and increases thermal expansion by adding the above-mentioned molten calcia or calcia clinker to the investment material. It is something to do.

(発明の構成) この発明は、溶融カルシアまたはカルシアクリンカ−か
らなることを特徴とする埋没材用加熱膨張性付与剤であ
る。
(Structure of the Invention) The present invention is a heat-expandability imparting agent for investment materials, characterized by comprising molten calcia or calcia clinker.

溶融カルシアはCa098%以上にして不純物としてM
gO,5i02、A120g、Fe20gなどを少量含
んだものであり、溶鋼の精練剤として一般に市販されて
いる。またカルシアクリンカ−はCa090%以上にし
て上記TiO+、Fe2O2などの化合物を添加して焼
結したものであり、耐消化性が優れたや金柑として一般
に使用されている。このカルシアクリンカ−は、上記化
合物を添加することによって焼成温度が低下するのでそ
の製造が比較的に容易である。
The molten calcia has Ca098% or more and M as an impurity.
It contains small amounts of gO, 5i02, 120 g of A, 20 g of Fe, etc., and is generally commercially available as a refining agent for molten steel. Calcia clinker is made by adding compounds such as TiO+ and Fe2O2 and sintering the Ca content to 90% or more, and is generally used as a kumquat with excellent digestion resistance. This calcia clinker is relatively easy to manufacture because the calcination temperature is lowered by adding the above compound.

上記加熱膨張性付与剤を混合した埋没材は、水またはコ
ロイダルシリカ溶液によって混練されてリングに充填さ
れ、常法によって加熱される。
The investment material mixed with the heat-expandability imparting agent is kneaded with water or a colloidal silica solution, filled into a ring, and heated by a conventional method.

(実施例) 実施例1 Si0280重量部、N1(41(2P0.10重量部
、Mg010重量部からなるリン酸塩系埋没材100重
量部に、各種加熱膨張性付与剤3重量部を混合し、この
混合理没材の加熱膨張率を測定し、加熱膨張率と温度と
の関係を第1図のグラフに示した。
(Example) Example 1 100 parts by weight of a phosphate-based investment material consisting of 280 parts by weight of Si0, 0.10 parts by weight of N1(41(2P), and 10 parts by weight of Mg) were mixed with 3 parts by weight of various thermal expandability imparting agents, The thermal expansion coefficient of this mixed sinking material was measured, and the relationship between the thermal expansion coefficient and temperature is shown in the graph of FIG.

グラフ&lの加熱膨張性付与剤は、タテホ化学工業社製
溶融カルシアFC^−8Aである。&2の加熱膨張性付
与剤は、Ca095重量部、Fe20B5重量部の混合
物を約200kg/cdの圧力を加えて成形し、140
0℃、4時間焼成し、冷却後200メツシユ以上に微粉
砕したカルシアクリンカ−であり、Nn 3の加熱膨張
性付与剤は、Ca092重量部、Fe20B 5重量部
およびTiO23重量部の混合物を、上記Nα2と同様
に焼成、粉砕したカルシアクリンカ−である。なおNα
4は加熱膨張性付与剤を添加しない比較餌である。
The heat expandability imparting agent of Graf&l is Fused Calcia FC^-8A manufactured by Tateho Chemical Industry Co., Ltd. The heat expandability imparting agent &2 is obtained by molding a mixture of 95 parts by weight of Ca0 and 5 parts by weight of Fe20B by applying a pressure of about 200 kg/cd.
Calcia clinker is calcined at 0°C for 4 hours, cooled, and then finely pulverized to 200 meshes or more. This is calcia clinker that has been calcined and crushed in the same way as Nα2. Note that Nα
No. 4 is a comparison bait to which no heat-expandability imparting agent was added.

加熱膨張率は、筆本秀和著報文[試作無膨張理没材を用
いての鋳造体の変形について」 (補綴誌第29巻第2
号、1980年、165〜185頁)中に記載されてい
る方法に準じて測定した。
The coefficient of thermal expansion is based on a report written by Hidekazu Fudemoto [About the deformation of cast bodies using prototype non-expandable sinking materials] (Prosthetics Journal Vol. 29, No. 2)
No., 1980, pp. 165-185).

第1図のグラフでみられるように、この発明の加熱膨張
性付与剤を添加したNα1.2.3は、無添加のNa 
4に比べて加熱膨張率が大きく、鋳造時の合金の収縮を
十分に補償できるものである。また加熱膨張率は温度1
50〜200℃で急激に上昇される。なお、上記混合理
没材の硬化膨張率はほとんど0であった。
As seen in the graph of Figure 1, Na1.2.3 to which the heat expandability imparting agent of the present invention is added is different from that of unadded Na.
It has a larger thermal expansion coefficient than No. 4, and can sufficiently compensate for the shrinkage of the alloy during casting. Also, the coefficient of thermal expansion is temperature 1
It is rapidly raised between 50 and 200°C. In addition, the hardening expansion coefficient of the mixed sinking material was almost 0.

実施例2 上記実施例1の溶融カルシア混合の埋没材において溶融
カルシアの混合率を変化した場合の加熱膨張率を測定し
、その結果を第2図のグラフに示した。加熱膨張性付与
剤の混合率を大きくすると加熱膨張率が大きくなるので
加熱膨張性付与剤の混合率を調節することによって所望
の加熱膨張率が得られる。
Example 2 The thermal expansion coefficient was measured when the mixing ratio of molten calcia was changed in the investment material mixed with molten calcia of Example 1, and the results are shown in the graph of FIG. Since increasing the mixing ratio of the heat-expandability imparting agent increases the heat-expansion coefficient, a desired heat-expansion coefficient can be obtained by adjusting the mixing ratio of the heat-expandability imparting agent.

(発明の効果) この発明の加熱膨張性付与剤は、リン酸塩系埋没材の加
熱膨張率を従来より向上させることができかつ硬化膨張
はほとんどないので鋳造時の合金の収縮を加熱膨張のみ
によって補償することが可能となる。また加熱膨張性付
与剤の混合量を変化することによって所望の加熱膨張率
が得られる。
(Effects of the Invention) The heat-expandability imparting agent of the present invention can improve the heat-expansion coefficient of phosphate-based investment materials compared to the conventional one, and has almost no hardening expansion, so the shrinkage of the alloy during casting is limited to heating expansion. It becomes possible to compensate by Further, a desired coefficient of thermal expansion can be obtained by changing the amount of the thermal expansion imparting agent mixed.

さらに加熱膨張性付与剤は従来溶鋼の精練用などに使用
されていたものであるから容易に入手することができる
Further, the heat-expandability imparting agent is one that has been conventionally used for refining molten steel and is therefore easily available.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は実施例1の加熱膨張率と温度との関係を示すグ
ラフ、第2図は実施例2の加熱膨張率と温度との関係を
示すグラフである。 第1図 温 度(’C) 第2図 温 度(0C)
FIG. 1 is a graph showing the relationship between the thermal expansion coefficient and temperature in Example 1, and FIG. 2 is a graph showing the relationship between the thermal expansion coefficient and temperature in Example 2. Figure 1 Temperature ('C) Figure 2 Temperature (0C)

Claims (1)

【特許請求の範囲】[Claims] (1)溶融カルシウムまたはカルシアクリンカ−からな
ることを特徴とする埋没材用加熱膨張性付与剤。
(1) A heat-expandability imparting agent for investment materials, characterized by comprising molten calcium or calcia clinker.
JP59022498A 1984-02-08 1984-02-08 Thermal expandability imparting agent for embedding material Granted JPS60166140A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59022498A JPS60166140A (en) 1984-02-08 1984-02-08 Thermal expandability imparting agent for embedding material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59022498A JPS60166140A (en) 1984-02-08 1984-02-08 Thermal expandability imparting agent for embedding material

Publications (2)

Publication Number Publication Date
JPS60166140A true JPS60166140A (en) 1985-08-29
JPH0155063B2 JPH0155063B2 (en) 1989-11-22

Family

ID=12084405

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59022498A Granted JPS60166140A (en) 1984-02-08 1984-02-08 Thermal expandability imparting agent for embedding material

Country Status (1)

Country Link
JP (1) JPS60166140A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4702304A (en) * 1986-11-03 1987-10-27 General Motors Corporation Foundry mold for cast-to-size zinc-base alloy

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS492655B1 (en) * 1970-12-30 1974-01-22
JPS5215442B2 (en) * 1974-08-24 1977-04-30
JPS572421B2 (en) * 1974-09-14 1982-01-16

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS492655A (en) * 1972-04-24 1974-01-10
FR2318656A1 (en) * 1975-07-25 1977-02-18 Comex Cie Maritime Expertises Underwater welding in submerged chamber - by welders who need no breathing masks due to purificn. of breathing gas mixt.
JPS572421A (en) * 1980-06-04 1982-01-07 Honda Motor Co Ltd Internal combustion engine

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS492655B1 (en) * 1970-12-30 1974-01-22
JPS5215442B2 (en) * 1974-08-24 1977-04-30
JPS572421B2 (en) * 1974-09-14 1982-01-16

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4702304A (en) * 1986-11-03 1987-10-27 General Motors Corporation Foundry mold for cast-to-size zinc-base alloy

Also Published As

Publication number Publication date
JPH0155063B2 (en) 1989-11-22

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