JPH082771B2 - Rapid heating type investment material composition - Google Patents
Rapid heating type investment material compositionInfo
- Publication number
- JPH082771B2 JPH082771B2 JP15141993A JP15141993A JPH082771B2 JP H082771 B2 JPH082771 B2 JP H082771B2 JP 15141993 A JP15141993 A JP 15141993A JP 15141993 A JP15141993 A JP 15141993A JP H082771 B2 JPH082771 B2 JP H082771B2
- Authority
- JP
- Japan
- Prior art keywords
- mold
- weight
- parts
- material composition
- investment material
- 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 - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims description 17
- 239000000463 material Substances 0.000 title claims description 16
- 238000010438 heat treatment Methods 0.000 title claims description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 45
- 239000010453 quartz Substances 0.000 claims description 16
- 229910052906 cristobalite Inorganic materials 0.000 claims description 14
- 239000011819 refractory material Substances 0.000 claims description 12
- 239000011230 binding agent Substances 0.000 claims description 11
- 229910052905 tridymite Inorganic materials 0.000 claims description 11
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 8
- 238000005266 casting Methods 0.000 description 6
- 239000010440 gypsum Substances 0.000 description 5
- 229910052602 gypsum Inorganic materials 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 4
- 239000008119 colloidal silica Substances 0.000 description 4
- 239000000395 magnesium oxide Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 229910001020 Au alloy Inorganic materials 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 239000003353 gold alloy Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229910000623 nickel–chromium alloy Inorganic materials 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000005495 investment casting Methods 0.000 description 1
- 238000005058 metal casting Methods 0.000 description 1
- 235000019837 monoammonium phosphate Nutrition 0.000 description 1
- 239000006012 monoammonium phosphate Substances 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
Landscapes
- Dental Preparations (AREA)
- Dental Prosthetics (AREA)
- Mold Materials And Core Materials (AREA)
Description
【0001】[0001]
【産業上の利用分野】この発明は、歯科用鋳型の成型に
使用される埋没材組成物に関し、上記鋳型の急速加熱を
可能にするものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an investment material composition used for molding a dental mold, which enables rapid heating of the mold.
【0002】[0002]
【従来の技術】歯科用鋳型の成型に使用される埋没材組
成物として、耐火材に石英やクリストバライトを単独で
または混合して使用し、結合材に石膏またはリン酸塩系
のものを使用したものが知られており、上記のクリスト
バライトや石英は、その熱膨張率が大きく、金属の鋳造
収縮を補償することができるという特長を備えているた
め、広く使用されている。2. Description of the Related Art As an investment material composition used for molding a dental mold, quartz or cristobalite is used alone or in a mixture as a refractory material, and a plaster or phosphate-based material is used as a binder. Cristobalite and quartz are widely used because they have a large coefficient of thermal expansion and can compensate for metal casting shrinkage.
【0003】[0003]
【発明が解決しようとする課題】しかしながら、石英
は、573℃でα型からβ型に転移するため、この温度
で熱膨張率が急上昇し、そのため石英を耐火材とする鋳
型を用いて融点が1000℃以上の金属、合金を鋳造す
る場合に、ワックスパターンの焼却および上記鋳型の予
熱を目的として鋳型を温度が700℃以上の電気炉に直
接入れて迅速に加熱しようとすると、鋳型に亀裂が発生
し、これを防ぐためには、2〜4時間の長時間をかけて
常温から700℃までゆっくり昇温させる必要があり、
きわめて非能率的であった。また、クリストバライト
は、220℃に転移点を有し、この温度で熱膨張率が急
上昇するため、上記の石英と同様の欠点を有していた。However, since quartz changes from α-type to β-type at 573 ° C., the coefficient of thermal expansion sharply rises at this temperature. Therefore, the melting point of quartz is increased by using a mold made of quartz as a refractory material. When casting a metal or alloy of 1000 ° C. or higher, if the mold is directly put into an electric furnace having a temperature of 700 ° C. or higher for the purpose of incineration of the wax pattern and preheating of the mold, and a rapid heating is performed, cracks are generated in the mold. In order to prevent this, it is necessary to slowly raise the temperature from room temperature to 700 ° C. over a long period of 2 to 4 hours,
It was extremely inefficient. Further, cristobalite has a transition point at 220 ° C., and the coefficient of thermal expansion sharply increases at this temperature, so that it has the same drawbacks as the above-mentioned quartz.
【0004】この発明は、熱膨張率が比較的小さいた
め、埋没材には不適当とされていたトリジマイトを上記
の耐火材に混用することにより、歯科用鋳型の急速加熱
を可能にし、鋳造時におけるワックスパターンの焼却お
よび鋳型の予熱に要する時間を大幅に短縮するものであ
る。In the present invention, since the thermal expansion coefficient is relatively small, tridymite, which has been considered unsuitable as an investment material, is mixed with the above refractory material, which enables rapid heating of the dental mold, and at the time of casting. The time required for incineration of the wax pattern and preheating of the mold in step 1 is greatly shortened.
【0005】[0005]
【課題を解決するための手段】すなわち、この発明は、
耐火材と結合材とからなり、上記耐火材が石英およびク
リストバライトの少なくとも一方にトリジマイトを添加
したものであることを特徴とする急速加熱型埋没材組成
物である。That is, the present invention provides:
A rapid heating type investment material composition comprising a refractory material and a binder, wherein the refractory material is obtained by adding tridymite to at least one of quartz and cristobalite.
【0006】この発明で使用する結合材は、石英やクリ
ストバライト等の耐火材に使用されているものと同様の
ものであり、マグネシアクリンカと第1リン酸アンモニ
ウムとの混合物等のリン酸塩系のもの、および石膏が好
適である。そして、上記結合材の配合量は、耐火材およ
び結合材の合計重量の10〜25%が好ましい。また、
トリジマイトの配合量は、耐火材および結合材の合計重
量の5〜50%が好ましい。The binder used in the present invention is the same as that used for refractory materials such as quartz and cristobalite, and is based on a phosphate-based material such as a mixture of magnesia clinker and monoammonium phosphate. The thing and gypsum are suitable. And, the compounding amount of the binder is preferably 10 to 25% of the total weight of the refractory material and the binder. Also,
The blending amount of tridymite is preferably 5 to 50% of the total weight of the refractory material and the binder.
【0007】[0007]
【作用】この発明の埋没材組成物は、結合材に石膏を使
用した場合は、水で練和して鋳型に成型される。また、
結合材にリン酸塩系のものを使用した場合は、コロイダ
ルシリカで練和して鋳型に成型される。しかして、この
発明で添加するトリジマイトは、熱膨張率が石英やクリ
ストバライトに比して小さく、かつ117℃および16
3℃の2点に転移点を有し、熱膨張率の上昇曲線が緩や
かであるため、鋳型を急速加熱する際の急激な熱膨張が
抑制され、亀裂の発生が防止される。ただし、トリジマ
イトの配合量が耐火材および結合材の合計重量の5%未
満の場合は、添加の効果がなく、反対に50%を超えた
場合は、鋳型全体の熱膨張が不足し、金属の鋳造収縮に
対する補償が不十分になる。When the investment material composition of the present invention uses gypsum as the binder, it is kneaded with water and molded into a mold. Also,
When a phosphate-based binder is used as the binder, it is kneaded with colloidal silica and molded into a mold. Thus, the tridymite added in the present invention has a smaller coefficient of thermal expansion than quartz and cristobalite, and has a temperature of 117 ° C and 16 ° C.
Since it has two transition points at 3 ° C. and the rising curve of the coefficient of thermal expansion is gentle, rapid thermal expansion at the time of rapidly heating the mold is suppressed, and cracks are prevented from occurring. However, if the blending amount of tridymite is less than 5% of the total weight of the refractory material and the binder, there is no effect of the addition. On the contrary, if it exceeds 50%, the thermal expansion of the entire mold is insufficient and the amount of metal Insufficient compensation for casting shrinkage.
【0008】[0008]
【実施例】実施例1 石英60重量部、クリストバライト10重量部、トリジ
マイト10重量部および石膏20重量部からなる埋没材
組成物100gにつき水32ccを加えて練和し、歯冠用
の鋳型を成型し、この鋳型を700℃の電気炉に入れ、
30分後に取出したところ、亀裂は全く認められなかっ
た。次いで、上記の鋳型に融点1000℃の金合金を注
いで鋳造し、精度の良好な歯冠を得た。Example 1 32 g of water was added to 100 g of an investment material composition consisting of 60 parts by weight of quartz, 10 parts by weight of cristobalite, 10 parts by weight of tridymite and 20 parts by weight of gypsum, and kneaded to form a mold for a crown. Then, put this mold in an electric furnace at 700 ° C,
When it was taken out after 30 minutes, no crack was observed. Then, a gold alloy having a melting point of 1000 ° C. was poured into the above-mentioned mold and cast to obtain a crown with good accuracy.
【0009】実施例2 石英60重量部、クリストバライト10重量部、トリジ
マイト10重量部、マグネシアクリンカ10重量部およ
び第1リン酸アンモニウム10重量部からなる埋没材組
成物100gにつきコロイダルシリカ20ccを加えて練
和し、歯冠用の鋳型を成型し、この鋳型を800℃の電
気炉に入れ、30分後に取出したところ、亀裂は全く認
められなかった。次いで、上記の鋳型に融点1300℃
のニッケルクロム合金を注いで鋳造し、精度の良好な歯
冠を得た。Example 2 20 cc of colloidal silica was added to 100 g of an investment material composition consisting of 60 parts by weight of quartz, 10 parts by weight of cristobalite, 10 parts by weight of tridymite, 10 parts by weight of magnesia clinker and 10 parts by weight of ammonium primary phosphate, and kneaded. When the mixture was soaked and a crown crown mold was molded, and the mold was put in an electric furnace at 800 ° C. and taken out after 30 minutes, no crack was observed at all. Then, the above-mentioned mold has a melting point of 1300 ° C.
A nickel-chromium alloy was poured and cast to obtain a highly accurate crown.
【0010】実施例3 石英60重量部、トリジマイト20重量部および石膏2
0重量部からなる埋没材組成物100gにつき水32cc
を加えて練和し、実施例1と同様に歯冠用の鋳型を成型
し、700℃の電気炉に入れて30分後に取出し、亀裂
が皆無の鋳型を得、融点1000℃の金合金からなる良
好な歯冠を鋳造した。Example 3 Quartz 60 parts by weight, tridymite 20 parts by weight and gypsum 2
32 cc of water per 100 g of investment material composition consisting of 0 parts by weight
Was added and kneaded, and a mold for a crown was molded in the same manner as in Example 1, put in an electric furnace at 700 ° C. and taken out after 30 minutes to obtain a mold without cracks. A gold alloy having a melting point of 1000 ° C. A good dental crown was cast.
【0011】実施例4 クリストバライト40重量部、トリジマイト40重量
部、マグネシアクリンカ10重量部および第1リン酸ア
ンモニウム10重量部からなる埋没材組成物100gに
つきコロイダルシリカ20ccを加えて練和し、実施例2
と同様に歯冠用の鋳型を成型し、800℃の電気炉に入
れて30分後に取出し、亀裂が皆無の鋳型を得、融点1
300℃のニッケルクロム合金からなる良好な歯冠を鋳
造した。Example 4 20 g of colloidal silica was added to 100 g of an investment material composition consisting of 40 parts by weight of cristobalite, 40 parts by weight of tridymite, 10 parts by weight of magnesia clinker and 10 parts by weight of ammonium primary phosphate, and kneaded. Two
Mold a dental crown mold in the same manner as in, place it in an electric furnace at 800 ° C and take it out after 30 minutes to obtain a mold without cracks, melting point 1
A good crown made of nickel-chromium alloy at 300 ° C was cast.
【0012】比較例1 クリストバライト80重量部および石膏20重量部から
なる埋没材組成物100gにつき水32ccを加えて練和
し、歯冠用の鋳型を成型し、この鋳型を700℃の電気
炉に入れて30分後に取出したところ、亀裂が発生して
使用不可能であった。ただし、常温から700℃まで2
時間以上の時間をかけてゆっくり昇温させた場合は、亀
裂の発生がなく、鋳造可能であった。Comparative Example 1 32 g of water was added to 100 g of an investment material composition consisting of 80 parts by weight of cristobalite and 20 parts by weight of gypsum and kneaded to form a mold for a crown, and the mold was placed in an electric furnace at 700 ° C. When it was taken out 30 minutes after being put in, it was unusable due to cracking. However, from room temperature to 700 ° C 2
When the temperature was slowly raised over the time, it was possible to cast without cracking.
【0013】比較例2 石英40重量部、クリストバライト40重量部、マグネ
シアクリンカ10重量部および第1リン酸アンモニウム
10重量部からなる埋没材組成物100gにつきコロイ
ダルシリカ20ccを加えて練和し、歯冠用の鋳型を成型
し、この鋳型を800℃の電気炉に入れて30分後に取
出したところ、亀裂が発生して使用不可能であった。そ
して、同様に成型した鋳型に亀裂を発生させないために
は、2時間以上の時間をかけてゆっくり昇温させる必要
があった。Comparative Example 2 20 cc of colloidal silica was added to 100 g of an investment composition consisting of 40 parts by weight of quartz, 40 parts by weight of cristobalite, 10 parts by weight of magnesia clinker and 10 parts by weight of ammonium monobasic phosphate, and kneaded to prepare a crown. A casting mold was molded, and the mold was put in an electric furnace at 800 ° C. and taken out after 30 minutes. As a result, a crack was generated and it was unusable. Then, in order to prevent cracks from being generated in the similarly molded mold, it was necessary to slowly raise the temperature over 2 hours or more.
【0014】[0014]
【発明の効果】上記のとおり、この発明の埋没材組成物
は、金属の鋳造収縮を補償する性能に優れた石英やクリ
ストバライトの一部を熱膨張率が比較的小さく、かつ温
度上昇に伴う熱膨張率の急激上昇がないトリジマイトで
置換したものであるから、上記の埋没材組成物で鋳型を
成型した場合、高温の電気炉に直接入れて急速に加熱し
ても亀裂の発生が無く、そのため鋳造に際し、鋳型の予
熱を兼ねたワックスパターンの焼却に要する時間を従来
の1/4以下に大幅に短縮することができ、しかも石英
やクリストバライト等の耐火材が備えている上記の補償
性能を損なうことがなく、高精度の鋳造が可能である。INDUSTRIAL APPLICABILITY As described above, the investment material composition of the present invention has a relatively small coefficient of thermal expansion of quartz and cristobalite, which is excellent in the capability of compensating the casting shrinkage of the metal, and has a thermal expansion coefficient which is accompanied by a temperature rise Since it is replaced with tridymite that does not have a rapid increase in expansion coefficient, when molding a mold with the above-mentioned investment material composition, there is no occurrence of cracks even if it is directly heated in a high-temperature electric furnace and rapidly heated. During casting, the time required to incinerate the wax pattern, which also serves to preheat the mold, can be greatly reduced to less than 1/4 of the conventional time, and the above compensation performance of the refractory material such as quartz and cristobalite is impaired. And high-precision casting is possible.
Claims (1)
が石英およびクリストバライトの少なくとも一方にトリ
ジマイトを添加したものであることを特徴とする急速加
熱型埋没材組成物。1. A rapid heating type investment material composition comprising a refractory material and a binder, wherein the refractory material is obtained by adding tridymite to at least one of quartz and cristobalite.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15141993A JPH082771B2 (en) | 1993-05-27 | 1993-05-27 | Rapid heating type investment material composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15141993A JPH082771B2 (en) | 1993-05-27 | 1993-05-27 | Rapid heating type investment material composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH06336409A JPH06336409A (en) | 1994-12-06 |
JPH082771B2 true JPH082771B2 (en) | 1996-01-17 |
Family
ID=15518211
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15141993A Expired - Lifetime JPH082771B2 (en) | 1993-05-27 | 1993-05-27 | Rapid heating type investment material composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH082771B2 (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3529523B2 (en) * | 1995-11-17 | 2004-05-24 | 株式会社ジーシー | Dental phosphate investment composition |
JP3524293B2 (en) * | 1995-11-17 | 2004-05-10 | 株式会社ジーシー | Dental gypsum investment composition |
GB2379628A (en) * | 2001-08-08 | 2003-03-19 | Micro Metalsmiths Ltd | Investment casting |
JP4294037B2 (en) | 2006-06-13 | 2009-07-08 | 大成歯科工業株式会社 | Phosphate-based dental investment |
JP5276147B2 (en) * | 2011-07-15 | 2013-08-28 | キヤノンプレシジョン株式会社 | Automated traveling vehicle and automated traveling system |
CN104245184A (en) | 2012-04-27 | 2014-12-24 | 吉野石膏株式会社 | Gypsum-based embedding material composition for casting |
JP6125500B2 (en) | 2012-06-18 | 2017-05-10 | 吉野石膏株式会社 | Casting investment composition and casting method using the same |
-
1993
- 1993-05-27 JP JP15141993A patent/JPH082771B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH06336409A (en) | 1994-12-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR101632543B1 (en) | Casting investment composition and casting process using same | |
CA1146782A (en) | Dental appliance and method of manufacture | |
JPH082771B2 (en) | Rapid heating type investment material composition | |
US9834480B2 (en) | Gypsum-based embedding material composition for casting | |
US6291378B1 (en) | Dental restorations | |
JP2857872B2 (en) | Dental investment | |
US3647488A (en) | Dental prosthesis model base composition containing calcium fluoride | |
JP3447769B2 (en) | Dental investment composition | |
US1962764A (en) | Investment | |
US1932202A (en) | Investment | |
JP3114055B2 (en) | Dental investment material and dental mold | |
JP2578076B2 (en) | Dental refractory profile | |
JP2003034608A (en) | Flash heating-type phosphate investment for dental use | |
JP4195546B2 (en) | Plaster investment for dental casting | |
JPS5992144A (en) | Composition of embedding material for precision casting | |
SU993942A1 (en) | Composition for casting dentures | |
JPS6382653A (en) | Calcium phosphate-based investment material for glass casting | |
JPH06191925A (en) | Method for forming formed ceramic article | |
JPH04327514A (en) | High temperature investment material | |
SU1017317A1 (en) | Composition for casting tooth prosthesises | |
JPS6293041A (en) | Molding material for casting pure titanium or titanium alloy | |
JPH0429617B2 (en) | ||
JPH0437435A (en) | Investment for dentistry casting | |
JPS60208902A (en) | Dental casting investment material composition with large coefficient of thermal expansion | |
JPS61147943A (en) | Hardener liquid of molding material for dental purpose |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20080117 Year of fee payment: 12 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20090117 Year of fee payment: 13 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20090117 Year of fee payment: 13 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20100117 Year of fee payment: 14 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20100117 Year of fee payment: 14 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110117 Year of fee payment: 15 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110117 Year of fee payment: 15 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20120117 Year of fee payment: 16 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20120117 Year of fee payment: 16 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20130117 Year of fee payment: 17 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20140117 Year of fee payment: 18 |
|
EXPY | Cancellation because of completion of term |