JP2003034608A - Flash heating-type phosphate investment for dental use - Google Patents
Flash heating-type phosphate investment for dental useInfo
- Publication number
- JP2003034608A JP2003034608A JP2001253636A JP2001253636A JP2003034608A JP 2003034608 A JP2003034608 A JP 2003034608A JP 2001253636 A JP2001253636 A JP 2001253636A JP 2001253636 A JP2001253636 A JP 2001253636A JP 2003034608 A JP2003034608 A JP 2003034608A
- Authority
- JP
- Japan
- Prior art keywords
- phosphate
- investment material
- dental
- based investment
- rapid heating
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 229910019142 PO4 Inorganic materials 0.000 title claims abstract description 45
- 239000010452 phosphate Substances 0.000 title claims abstract description 44
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 title claims abstract description 43
- 238000010438 heat treatment Methods 0.000 claims abstract description 41
- 239000000395 magnesium oxide Substances 0.000 claims abstract description 17
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims abstract description 17
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims abstract description 17
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000000463 material Substances 0.000 claims description 71
- 239000002245 particle Substances 0.000 claims description 28
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 27
- 238000005266 casting Methods 0.000 claims description 26
- 238000004898 kneading Methods 0.000 claims description 13
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 12
- 239000008119 colloidal silica Substances 0.000 claims description 10
- 239000007788 liquid Substances 0.000 claims description 9
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 claims description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 4
- 239000005350 fused silica glass Substances 0.000 claims description 3
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 claims description 2
- 229910052863 mullite Inorganic materials 0.000 claims description 2
- 150000003016 phosphoric acids Chemical class 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 abstract description 13
- 239000002184 metal Substances 0.000 abstract description 13
- 239000003015 dental casting investment Substances 0.000 abstract description 2
- 235000021317 phosphate Nutrition 0.000 description 34
- 238000000034 method Methods 0.000 description 22
- 230000035939 shock Effects 0.000 description 12
- 239000004254 Ammonium phosphate Substances 0.000 description 9
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 9
- 235000019289 ammonium phosphates Nutrition 0.000 description 9
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 9
- 239000010440 gypsum Substances 0.000 description 9
- 229910052602 gypsum Inorganic materials 0.000 description 9
- 229910045601 alloy Inorganic materials 0.000 description 7
- 239000000956 alloy Substances 0.000 description 7
- 239000011230 binding agent Substances 0.000 description 6
- 229910052906 cristobalite Inorganic materials 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 150000002739 metals Chemical class 0.000 description 6
- 239000000470 constituent Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- ZOMBKNNSYQHRCA-UHFFFAOYSA-J calcium sulfate hemihydrate Chemical compound O.[Ca+2].[Ca+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O ZOMBKNNSYQHRCA-UHFFFAOYSA-J 0.000 description 4
- 235000012239 silicon dioxide Nutrition 0.000 description 4
- 239000010425 asbestos Substances 0.000 description 3
- 238000009933 burial Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000010453 quartz Substances 0.000 description 3
- 239000011819 refractory material Substances 0.000 description 3
- 229910052895 riebeckite Inorganic materials 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 229940099259 vaseline Drugs 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- -1 calcium phosphate compound Chemical class 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- 238000005498 polishing Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- 235000012255 calcium oxide Nutrition 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 210000004268 dentin Anatomy 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000005495 investment casting Methods 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000002694 phosphate binding agent Substances 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 229910021332 silicide Inorganic materials 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- GBNXLQPMFAUCOI-UHFFFAOYSA-H tetracalcium;oxygen(2-);diphosphate Chemical compound [O-2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GBNXLQPMFAUCOI-UHFFFAOYSA-H 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 239000001226 triphosphate Substances 0.000 description 1
- 235000011178 triphosphate Nutrition 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
- RUDFQVOCFDJEEF-UHFFFAOYSA-N yttrium(III) oxide Inorganic materials [O-2].[O-2].[O-2].[Y+3].[Y+3] RUDFQVOCFDJEEF-UHFFFAOYSA-N 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
Landscapes
- Dental Preparations (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は高融点の金属を鋳造
する歯科用リン酸塩系埋没材に関する。特に、埋没後2
0〜30分後に埋没したリングを800〜1000℃の
ファーネスに直接投入する急速加熱型のリン酸塩系埋没
材に関する。TECHNICAL FIELD The present invention relates to a dental phosphate-based investment material for casting a metal having a high melting point. Especially after burial 2
The present invention relates to a rapid heating type phosphate-based investment material in which a ring buried after 0 to 30 minutes is directly put into a furnace at 800 to 1000 ° C.
【0002】[0002]
【従来の技術】陶材焼き付け用合金として用いられる高
融点の金属を鋳造するためにはリン酸塩系埋没材を用い
られてきた。リン酸塩系埋没材の組成は、結合材として
酸化マグネシウムと第1リン酸アンモニウム、耐火材
(骨材)としてシリカ、アルミナ、ジルコン等を含むも
のであり、専用液としてコロイダルシリカで練和するこ
とも特徴的でである。この埋没材の利点として、専用液
のコロイダルシリカの濃度を調節することにより、様々
な金属の鋳造収縮に見合った総合膨張を得ることがる。
たとえば、金を主体とするプレシャス合金からニッケ
ル、コバルトを主体とするノンプレシャス合金まで幅広
く使用できる。2. Description of the Related Art Phosphate-based investment materials have been used for casting high melting point metals used as porcelain baking alloys. The composition of the phosphate-based investment material includes magnesium oxide and primary ammonium phosphate as a binder, silica, alumina, zircon as a refractory material (aggregate), and is mixed with colloidal silica as a dedicated liquid. That is also characteristic. As an advantage of this investment material, by adjusting the concentration of colloidal silica in the dedicated liquid, it is possible to obtain a total expansion that matches casting shrinkage of various metals.
For example, it can be widely used from precious alloys mainly composed of gold to non-precious alloys mainly composed of nickel and cobalt.
【0003】ノンプレシャス合金の鋳造収縮を補うには
2.5%以上の総合膨張を必要とする。通常のリン酸塩
系埋没材としては、熱膨張量を1.5%以上上げること
が難しいことから、専用液から得られる硬化膨張を期待
しなければならない。専用液のみで練和したときに、リ
ン酸塩系埋没材の熱膨張量に加え、硬化膨張を1.5%
以上を膨張させる様に調整し、金属の膨張・収縮量に合
わせて希釈して用いるのが通法である。A total expansion of 2.5% or more is required to compensate for the casting shrinkage of the non-precious alloy. Since it is difficult to increase the thermal expansion amount by 1.5% or more for a normal phosphate-based investment material, it is necessary to expect a hardening expansion obtained from a dedicated liquid. When kneaded only with the dedicated liquid, the thermal expansion amount of the phosphate-based investment material plus the hardening expansion of 1.5%
It is customary to adjust the above so that it expands and dilute it according to the amount of expansion and contraction of the metal.
【0004】この他に代表的な埋没材として石こう系埋
没材があり、これは高温で分解するために高温では使用
できない。しかし、比較的安価であるため、低融点(1
000〜1100℃)の金属には石こう系埋没材が用い
られ、高融点(1100℃以上)の金属にはリン酸塩系
埋没材を用いるのが通例である。近年、石こう系埋没材
は短時間鋳造法すなわち急速加熱型と呼ばれる埋没材が
主流となりつつある。通常であれば、石こう系埋没材は
ノーマル加熱鋳造法により行われる。In addition to this, a typical investment material is a gypsum investment material, which cannot be used at high temperatures because it decomposes at high temperatures. However, since it is relatively inexpensive, it has a low melting point (1
It is customary to use a gypsum-based investment material for metals of 000 to 1100 ° C. and a phosphate-based investment material for metals of high melting point (1100 ° C. or higher). In recent years, as the gypsum-based investment material, a short-time casting method, that is, an investment material called a rapid heating type is becoming mainstream. Normally, the gypsum-based investment material is produced by the normal heating casting method.
【0005】ノーマル加熱鋳造法とは埋没終了後、1時
間程度放置し、それからファーネスに入れ室温から1.
5〜2時間かけて700℃の温度に達するように加熱
し、30分係留してから鋳造するものである。ところ
が、最近短時間鋳造法(以下急速加熱鋳造法と呼ぶ)と
呼ばれる鋳造法が主流となってきた。急速加熱鋳造法と
は技工作業の大幅な短縮を目的として、埋没後20〜3
0分後に700℃のファーネスにリングを直接投入する
方法のことである。近年、石こう系埋没材においても、
急速加熱型の技術が発展しており、数々の問題点を克服
しており、短時間で強度を有するように設計され、急硬
化性を付与されるようになった。What is the normal heating casting method? After the burial is completed, it is left for about 1 hour, then put in a furnace and from room temperature to 1.
It is heated for 5 to 2 hours to reach a temperature of 700 ° C., moored for 30 minutes, and then cast. However, recently, a casting method called a short time casting method (hereinafter referred to as a rapid heating casting method) has become mainstream. The rapid heating casting method is used for the purpose of drastically shortening the technical work, and it is 20 ~ 3
It is a method of directly inserting the ring into the furnace at 700 ° C. after 0 minutes. In recent years, even in gypsum-based investment materials,
Rapid heating type technology has been developed, overcomes various problems, is designed to have strength in a short time, and has been rapidly hardened.
【0006】表面性状においては、石こう系埋没材の場
合、結合材は半水石こうを主成分としているため主に水
和反応により凝固反応が生じる。したがって埋没材を短
時間で熱衝撃を加えても水和反応を急激に促進するだけ
であるため、鋳造体の鋳肌荒れを生じることはあまり問
題にならなかった。Regarding the surface properties, in the case of a gypsum-based investment material, the binder mainly contains hemihydrate gypsum, so that a solidification reaction mainly occurs by a hydration reaction. Therefore, even if a heat shock is applied to the investment material for a short time, the hydration reaction is only accelerated rapidly, so that the roughening of the casting surface of the cast body is not a serious problem.
【0007】一方、リン酸塩系埋没材は従来のノーマル
加熱鋳造法がまだ多いものの、急速加熱鋳造法が急速に
普及しつつある。リン酸塩系埋没材のノーマル加熱とは
埋没終了後、1時間程度放置し、それからファーネスに
入れ室温から1.5〜2時間かけて800〜900℃の
温度に達するように加熱し、30分係留してから鋳造す
るものである。On the other hand, as for the phosphate-based investment material, although there are still many conventional normal heating casting methods, the rapid heating casting method is rapidly becoming popular. Normal heating of phosphate-based investment material is left for about 1 hour after the investment is completed, then put in a furnace and heated from room temperature to 800-900 ° C over 1.5-2 hours, 30 minutes It is moored and then cast.
【0008】これに対し、急速加熱鋳造法は埋没後20
〜30分後に800〜900℃のファーネスにリングを
直接投入するものである。しかし、リン酸塩系埋没材は
先に述べた酸化マグネシウムと第1リン酸アンモニウム
を結合材としているため、短時間でファーネスに投入す
るには短時間で硬化させる必要がある。リン酸塩系埋没
材を急速加熱した場合、表面性状は通常加熱した場合よ
りも滑沢でないことが問題であった。On the other hand, in the rapid heating casting method, 20 hours after burial
After about 30 minutes, the ring is directly put into the furnace at 800 to 900 ° C. However, since the phosphate-based investment material uses the above-described magnesium oxide and the first ammonium phosphate as a binder, it needs to be hardened in a short time in order to put it in the furnace in a short time. When the phosphate-based investment material was rapidly heated, there was a problem that the surface texture was less smooth than when it was normally heated.
【0009】また、結合材を減少させた場合、硬化膨張
量が減少してしまい、ノンプレシャス合金の鋳造収縮を
補うことが難しい状態であった。今までのリン酸塩など
の無機塩を用いる方法は反応性に問題があり、急速加熱
を行った場合、表面性状が悪くなることやヒートショッ
クに弱いという問題を抱えていた。Further, when the amount of the binder is reduced, the amount of hardening expansion is reduced, and it is difficult to compensate the casting shrinkage of the non-precious alloy. The conventional methods using inorganic salts such as phosphates have problems in reactivity, and when rapid heating is performed, they have problems in that the surface properties deteriorate and they are weak against heat shock.
【0010】表面性状を改善する方法と耐火度を上げる
方法は代表的には特開昭59−181203に公開され
ており、半水石こうをベースとして、これに酸性リン酸
アルミニウムを加えることによって解決している。しか
し、硬化性が悪く、急速加熱をすると亀裂、クラックを
生じ、ヒートショックに弱いという問題点を抱えてい
た。A method for improving the surface properties and a method for increasing the fire resistance are typically disclosed in JP-A-59-181203, which is solved by adding hemihydrate gypsum as a base and adding acidic aluminum phosphate. is doing. However, it has a problem that it is poor in curability, cracks and cracks are formed when it is rapidly heated, and it is susceptible to heat shock.
【0011】高い総合膨張を得ることを目的とする方法
が特開昭63−141906に公開されており、半水石
こうもしくはリン酸塩系の結合材をベースとして、耐火
度を上げる耐火材を加え、膨張材として天然でんぷん及
び周期律表第IV、V、VI族の遷移金属の炭化物、窒
化物、硼化物、珪化物、硫化物を加える方法がある。し
かし、でんぷんの添加は膨張が不安定になるという問題
点を抱えていた。A method aiming at obtaining a high total expansion is disclosed in Japanese Patent Laid-Open No. 63-141906, and a refractory material for increasing the fire resistance is added based on a hemihydrate gypsum or phosphate binder. There is a method of adding natural starch as an expansive material and carbides, nitrides, borides, silicides and sulfides of transition metals of Groups IV, V and VI of the Periodic Table. However, the addition of starch has a problem that the expansion becomes unstable.
【0012】耐熱性と滑沢な表面性状を得る方法が特開
平2−207010に公開されており、カルシウムとリ
ンのモル比が1.5〜2.0であるリン酸カルシウム化
合物をα型リン酸三カルシウムとリン酸四カルシウムを
結合材として用いる。しかし、この方法でも硬化性が悪
く、急速加熱では亀裂が入るという問題点を抱えてい
た。A method for obtaining heat resistance and a smooth surface property is disclosed in JP-A-2-207010, and a calcium phosphate compound having a molar ratio of calcium to phosphorus of 1.5 to 2.0 is used as an α-type triphosphate. Calcium and tetracalcium phosphate are used as binders. However, even with this method, the curability is poor, and there is a problem in that cracks are formed by rapid heating.
【0013】表面への金属の焼き付きの克服方法が特開
平4−327514に公開されており、通常のリン酸塩
系埋没材に酸化アルミニウムを加え、なおかつクリスト
バライト及び酸化アルミニウムの平均粒径が2〜40μ
mであることで解決している。しかし、表面の焼き付き
は防止できるが、表面性状の向上は十分ではなかった。A method for overcoming the seizure of metal on the surface is disclosed in JP-A-4-327514, and aluminum oxide is added to a usual phosphate-based investment material, and the average particle size of cristobalite and aluminum oxide is 2 to. 40μ
It is solved by being m. However, although the seizure of the surface can be prevented, the improvement of the surface property was not sufficient.
【0014】石こう系埋没材においては石こうの熱分解
ガスを防止することにより高融点の金属を鋳造できるよ
う試みられた方法が特開平9−220638に公開され
ている。しかし、半水石こうをベースとして耐火度を上
げる方法は、十分な硬化膨張が得られず、高融点の金属
の溶解状態により表面性状が悪くなるという問題点があ
った。また、熱分解ガスを防止する得策を多種試みられ
ているが、未だ通常の使用に到る解決には到っていない
のが現状である。Japanese Unexamined Patent Publication No. 9-220638 discloses a method of casting a high melting point metal in a gypsum-based investment material by preventing pyrolysis gas of the gypsum. However, the method of increasing the fire resistance based on hemihydrate gypsum has a problem that sufficient hardening expansion cannot be obtained and the surface quality is deteriorated due to the molten state of the metal having a high melting point. In addition, various attempts have been made to prevent thermal decomposition gas, but the present situation is that it has not been solved yet for normal use.
【0015】熱膨張においては、練和液で調整するた
め、ある程度適した熱膨張を有する埋没材が望まれてい
るが、リン酸塩系埋没材においては、他の要望を同時に
解決された埋没材は報告されていない。更にリン酸塩系
埋没材で急速加熱型の技術は発展しておらず、数々の問
題点を抱えており、ヒートショックや、ヒビ割れ、表面
性状などを同時に解決できるものは無かった。特に表面
性状が安定した鋳造体を得る方法においては、解決する
ことは容易でないことである。In the thermal expansion, an investment material having a certain degree of suitable thermal expansion is desired because it is adjusted by a kneading liquid, but in the case of the phosphate-based investment material, an investment material which has solved other needs at the same time. No timber has been reported. Furthermore, the rapid heating type technology of phosphate-based investment materials has not been developed and has various problems, and there is no one that can simultaneously solve heat shock, cracking, surface texture and the like. In particular, it is not easy to solve the problem in a method of obtaining a cast body having stable surface properties.
【0016】総合膨張特に熱膨張量を確保することが難
しく、ヒートショックにより割れやひびが入ることが多
かった。ある程度、調整がされたものであっても膨張が
不安定になり、安定して使用できないものであった。亀
裂、クラックを生じることが多くそれらを解決するもの
はなかった。要望により、これらの問題点を解決するだ
けでなく、短時間で硬化させる必要があるが硬化性のよ
いものはなかった。表面の焼き付けを防止する事と表面
性状が良好であることを兼ね備えることは解決されてい
ない。Total expansion It is difficult to secure a particular amount of thermal expansion, and cracks and cracks often occur due to heat shock. Even if it was adjusted to some extent, the expansion became unstable and it could not be used stably. There were many cracks and cracks, and there was no solution to them. In addition to solving these problems, it was necessary to cure them in a short time, but none of them had good curability. It has not been solved to prevent the surface from being baked and to have a good surface property.
【0017】[0017]
【発明が解決しようとする課題】本発明は、十分な膨張
が得られ、表面に金属の焼き付きが起こる危険性が無
く、リン酸塩系埋没材の表面性状を向上させ、高い総合
膨張を得られ、かつ急速加熱を可能にすることが課題で
ある。リン酸塩系埋没材において、表面性状を向上させ
ることや、十分な硬化膨張を得られることが望まれてい
る。なおかつ、急速加熱をしても亀裂やクラックのない
ヒートショックに強い歯科用急速加熱型リン酸塩系埋没
材は開発されていない。DISCLOSURE OF THE INVENTION According to the present invention, sufficient expansion is obtained, there is no risk of metal sticking to the surface, the surface properties of the phosphate-based investment material are improved, and a high overall expansion is obtained. And to enable rapid heating. In a phosphate-based investment material, it is desired to improve the surface properties and obtain sufficient curing expansion. Moreover, no rapid-heating dental phosphate-based investment material for dental use, which is resistant to heat shock without cracks or cracks even when rapidly heated, has not been developed.
【0018】更にまた、精密な鋳造体を短時間で鋳造で
き、ヒートショックに強く、大きな総合膨張を得ること
が望まれており、より幅広い金属に使用でき、表面性状
が滑沢な鋳造体を得ることができる埋没材は、従来はな
く、これらの課題を解決することが望まれている。従来
の埋没材の利点に加え、硬化性がよく、急速加熱を可能
にし、表面性状が安定した鋳造体を得られ、膨張量を確
保し、ヒートショックにより割れやひびが無く、膨張が
安定に発現し、亀裂、クラックを生じることなく、練和
後、鋳型の形態付与後は、短期間で硬化し形態が安定
し、表面の焼き付けが発生せず、表面性状が良好である
ことを兼ね備えることを課題とする。また、本発明は急
速加熱を行うのに適当な硬化時間を有し、鋳造時には高
い圧縮強度を有し、鋳造後は掘り出しやすい埋没材を創
製することである。Furthermore, it is desired that a precision cast body can be cast in a short time, it is resistant to heat shock, and a large total expansion is obtained. It can be used for a wider range of metals and has a smooth surface property. There is no investment material that can be obtained, and it is desired to solve these problems. In addition to the advantages of conventional investment materials, it has a good hardening property, enables rapid heating, can obtain a cast product with stable surface properties, secures an expansion amount, does not crack or crack due to heat shock, and has a stable expansion It develops, cracks, and without kneading, after kneading, after imparting the morphology of the mold, the morphology is stable in a short period of time, the morphology is stable, surface baking does not occur, and it also has a good surface property. Is an issue. Further, the present invention is to create an investment material that has an appropriate curing time for performing rapid heating, has high compressive strength during casting, and is easy to dig after casting.
【0019】[0019]
【課題の解決手段】これらの課題について本発明者らは
鋭意研究の結果、本発明に到ることができた。本発明
は、歯科鋳造用埋没材であって、(a)酸化マグネシウ
ム、(b)第1リン酸アンモニウム(c)骨材を含むリ
ン酸塩系埋没材において、(a)平均粒径が10〜40
μmである酸化マグネシウム(b)第1リン酸アンモニ
ウムの内25μm以下が全第1リン酸アンモニウムに対
して10〜45重量%であることを特徴とする歯科用急
速加熱型リン酸塩系埋没材である。Means for Solving the Problems As a result of earnest research on these problems, the present inventors were able to reach the present invention. The present invention relates to a dental casting investment material, which is (a) magnesium oxide, (b) a first ammonium phosphate (c) a phosphate-based investment material containing an aggregate, wherein (a) the average particle size is 10: ~ 40
The rapid heating type phosphate-based investment material for dental use, wherein 25 μm or less of the magnesium oxide (b) monobasic ammonium phosphate having a diameter of 10 μm is 10 to 45% by weight with respect to the total ammonium phosphate. Is.
【0020】好ましい本発明の歯科用急速加熱型リン酸
塩系埋没材は、(a)酸化マグネシウムが平均粒径20
〜30μmであり、且つ100μm以上の粒子が1%以
内であり、(b)第1リン酸アンモニウムが60μm以
下であり、且つ25μm以下が全第1リン酸アンモニウ
ムに対して20〜35重量%であることを特徴とする歯
科用急速加熱型リン酸塩系埋没材である。好ましい本発
明は歯科用急速加熱型リン酸塩系埋没材であって、
(a)酸化マグネシウムが5〜15重量%(b)第1リ
ン酸アンモニウム10〜20重量%である歯科用急速加
熱型リン酸塩系埋没材である。The preferred dental rapid heating phosphate-based investment material of the present invention comprises (a) magnesium oxide having an average particle size of 20.
˜30 μm and 100 μm or more of particles are 1% or less, (b) ammonium monophosphate is 60 μm or less, and 25 μm or less is 20 to 35% by weight with respect to the total ammonium monophosphate. A rapid-heating dental phosphate-based investment material for dental use. The present invention is preferably a dental rapid heating phosphate-based investment material,
(A) 5 to 15% by weight of magnesium oxide (b) 10 to 20% by weight of ammonium monobasic phosphate, which is a rapid heating phosphate-type investment material for dental use.
【0021】本発明は歯科用急速加熱型リン酸塩系埋没
材であって(c)骨材がジルコニア、ケイ酸ジルコニウ
ム、溶融石英、ムライト、アルミナから選ばれた1種以
上を含むことを特徴とする歯科用急速加熱型リン酸塩系
埋没材である。更に、本発明は歯科用急速加熱型リン酸
塩系埋没材を練和する専用液としてコロイダルシリカ溶
液を用い、そのコロイダルシリカの平均粒径が70〜1
00nmである歯科用急速加熱型リン酸塩系埋没材であ
ることが好ましい。The present invention is a rapid heating phosphate-type investment material for dental use, wherein the aggregate (c) contains at least one selected from zirconia, zirconium silicate, fused silica, mullite and alumina. It is a rapid heating type phosphate-based investment material for dentistry. Further, the present invention uses a colloidal silica solution as a dedicated liquid for kneading a dental rapid heating phosphate-based investment material, and the average particle size of the colloidal silica is 70 to 1
It is preferably a rapid heating type phosphate-based investment material for dentin having a size of 00 nm.
【0022】[0022]
【発明の実施の形態】以下に本発明に係る歯科用急速加
熱型リン酸塩系埋没材について具体的に説明する。例示
されるものに関しては特に限定されるものではない。本
発明の(a)構成要件である酸化マグネシウムである
が、一般に歯科用で用いられる酸化マグネシウムは、純
度は高い方が好ましく、微細化してある方が好ましい。
100μm以上の粒子は粒度分布において1%以内であ
ることが好ましい。更に好ましくは100μm以上の粒
子を含まないことである。また、平均粒径は10〜40
μmであることが好ましく、20〜30μmであること
が更に好ましい。リン酸塩系埋没材全体への配合量は、
5〜15重量%あることが好ましい。BEST MODE FOR CARRYING OUT THE INVENTION The dental rapid heating type phosphate-based investment material according to the present invention will be specifically described below. The exemplified ones are not particularly limited. Regarding the magnesium oxide which is the constituent factor (a) of the present invention, the purity of magnesium oxide generally used for dentistry is preferably high, and it is preferable that it is finely divided.
Particles of 100 μm or more preferably have a particle size distribution of 1% or less. More preferably, it does not contain particles of 100 μm or more. The average particle size is 10-40
The thickness is preferably μm, more preferably 20 to 30 μm. The compounding amount in the whole phosphate-based investment material is
It is preferably 5 to 15% by weight.
【0023】次に、本発明の(b)構成要件である第1
リン酸アンモニウムであるが、第1リン酸アンモニウム
は可溶性であるが、埋没材の結合材で用いる場合、最大
粒径は小さいことが好ましい。リン酸塩系埋没材の表面
滑沢性より60μm以上の粒径のものが無いことが好ま
しい。さらに60μm以下の粒子の内、25μm以下の
粒子が10〜45重量%であることが好ましく、20〜
35重量%であることが更に好ましい。リン酸塩系埋没
材全体への配合量は、10〜20重量%あることが好ま
しい。Next, the first feature which is the (b) constituent requirement of the present invention
Although it is ammonium phosphate, the first ammonium phosphate is soluble, but when it is used as a bonding material for an investment material, it is preferable that the maximum particle size is small. Due to the surface lubricity of the phosphate-based investment material, it is preferable that there is no particle having a particle size of 60 μm or more. Further, of the particles of 60 μm or less, the amount of particles of 25 μm or less is preferably 10 to 45% by weight, and 20 to 20%
More preferably, it is 35% by weight. The content of the phosphate-based investment material in the whole is preferably 10 to 20% by weight.
【0024】次に、本発明の好ましい(a)構成要件と
(b)構成要件の配合比は重量比で(a)/(b)=
0.3〜1.0であることが好ましい。さらに好ましく
は、(a)/(b)=0.4〜0.8である。Next, the preferable composition ratio of (a) constituents and (b) constituents of the present invention is (a) / (b) = weight ratio.
It is preferably 0.3 to 1.0. More preferably, (a) / (b) = 0.4 to 0.8.
【0025】次にこれらの結合材を配合する(c)構成
要件である骨材であるが、歯科鋳造用の埋没材に使用さ
れる耐火材であればよく、具体的には石英、クリストバ
ライト、溶融石英、アルミナ、ジルコニア、ケイ酸ジル
コニウム、カルシア、イットリアなどがある。ジルコニ
ア、ケイ酸ジルコニウム、石英、クリストバライトが特
に好ましい。Next, the aggregate (c), which is a constituent of the binder, is a refractory material used as an investment material for dental casting. Specifically, quartz, cristobalite, Examples include fused silica, alumina, zirconia, zirconium silicate, calcia, and yttria. Zirconia, zirconium silicate, quartz and cristobalite are particularly preferred.
【0026】また、これら骨材の配合量であるが、急速
加熱型のリン酸塩系埋没材では、クリストバライトの配
合量は少ない方が良い。クリストバライトの配合量は1
5〜45%が好ましく、25〜35%が特に好ましい。
ジルコニア、ケイ酸ジルコニウムの配合量は5〜15%
が好ましい。Regarding the content of these aggregates, it is preferable that the content of cristobalite be small in the rapid heating type phosphate investment material. The amount of cristobalite is 1
5 to 45% is preferable, and 25 to 35% is particularly preferable.
The amount of zirconia and zirconium silicate is 5 to 15%
Is preferred.
【0027】さらに、これらの埋没材としての粉材を練
和する液材であるが、コロイダルシリカ水溶液が上げら
れる。本発明を達せしめるためには高い硬化膨張と急速
加熱を並立するため、大粒径コロイダルシリカを用いる
ことが好ましい。コロイダルシリカの平均粒径は10n
m〜120nmが好ましく、70nm〜100nmが特
に好ましい。また、コロイダルシリカ濃度は20〜50
重量%が好ましく、35〜45重量%が特に好ましい。Further, a colloidal silica aqueous solution is a liquid material for kneading these powder materials as an investment material. In order to achieve the present invention, it is preferable to use a large particle size colloidal silica because high curing expansion and rapid heating are performed in parallel. The average particle size of colloidal silica is 10n
m-120 nm is preferable and 70 nm-100 nm is especially preferable. The colloidal silica concentration is 20 to 50.
%, Preferably 35 to 45% by weight.
【0028】本発明により得られる効果としては、30
分以内で800℃〜1000℃のファーネスに直接投入
でき、硬化膨張が1.5%以上得られ、なおかつ表面性
状が滑沢なものが得られる。The effect obtained by the present invention is 30
Within a minute, it can be directly put into a furnace at 800 to 1000 ° C., curing expansion of 1.5% or more can be obtained, and smooth surface properties can be obtained.
【0029】[0029]
【実施例】以下に、本発明を実施例によって説明するが
本発明はこれら実施例に限定されるものではない。な
お、酸化マグネシウムの粒度測定は、日機装製マイクロ
トラックHRA型を用い、第1リン酸アンモニウムの篩
いはJISの標準篩いを用いた。EXAMPLES The present invention will be described below with reference to examples, but the present invention is not limited to these examples. In addition, the particle size of magnesium oxide was measured using a Nikkiso Microtrac HRA type, and the first ammonium phosphate sieve was a JIS standard sieve.
【0030】試料1の調整
酸化マグネシウム原料を粉砕し、分級して、平均粒径が
25μm、100μm以上の粒子の頻度を1%以内に調
整した。Preparation of Sample 1 The magnesium oxide raw material was pulverized and classified to adjust the frequency of particles having an average particle diameter of 25 μm and 100 μm or more within 1%.
【0031】試料2の調整
第1リン酸アンモニウムを粉砕し、250メッシュ(6
0μm)を全通し、25μm(500メッシュ)篩い下
の粒子が30重量%になるように調整した。Preparation of Sample 2 The first ammonium phosphate was crushed to obtain 250 mesh (6
0 μm) was passed through, and the amount of particles under a 25 μm (500 mesh) sieve was adjusted to 30% by weight.
【0032】試料3の調整
酸化マグネシウムの粉砕
酸化マグネシウム原料を粉砕し、分級して、平均粒径が
45μm、100μm以上の粒子の頻度を1%以内に調
整した。Preparation of Sample 3 Magnesium Oxide Grinding A magnesium oxide raw material was crushed and classified to adjust the frequency of particles having an average particle diameter of 45 μm and 100 μm or more within 1%.
【0033】試料4の調整
第1リン酸アンモニウムを粉砕し、125メッシュ(1
25μm)を全通し、25μm(500メッシュ)篩い
下の粒子が5重量%になるように調整した。Preparation of Sample 4 First ammonium phosphate was pulverized to 125 mesh (1
25 μm), and the particles under a 25 μm (500 mesh) sieve were adjusted to be 5% by weight.
【0034】試料5の調整
第1リン酸アンモニウムを粉砕し、125メッシュ(1
25μm)を全通し、25μm(500メッシュ)篩い
下の粒子が50重量%になるように調整した。Preparation of Sample 5 First ammonium phosphate was pulverized to 125 mesh (1
25 μm), and the amount of particles under a 25 μm (500 mesh) sieve was adjusted to 50% by weight.
【0035】クリストバライト(200メッシュ(77
μm)全通)、石英(200メッシュ(77μm)全
通)、ケイ酸ジルコニウム(200メッシュ(77μ
m)全通)、ジルコニア(200メッシュ(77μm)
全通)及び試料1〜5を以下の組成にて配合した。Cristobalite (200 mesh (77
μm) all through), quartz (200 mesh (77 μm) all through), zirconium silicate (200 mesh (77 μm)
m) all through), zirconia (200 mesh (77 μm)
All) and Samples 1 to 5 were blended in the following composition.
【0036】[0036]
【表1】 [Table 1]
【0037】[0037]
【表2】 [Table 2]
【0038】[0038]
【表3】 [Table 3]
【0039】練和液は、日産化学製スノーテックスZL
(無水ケイ酸40重量%、平均粒子径90nm)、及び
日産化学製スノーテックス30(無水ケイ酸30重量
%、平均粒子径30nm)を用いた。鋳型の試験方法は
日本工業規格「歯科鋳造用石こう系埋没材」T6601
−1998に準拠した。すなわち硬化時間、圧縮強さは
これに準拠し、熱膨張については800℃まで昇温さ
せ、その数値を読みとった。埋没材練和方法は混液比2
2mL/100g粉でスノーテックスZLを練和液Aと
し、スノーテックス30を練和液Bとした。真空攪拌器
は松風パワーリフトミキサーを用い、練和時間は30秒
とした。The kneading solution is Snowtex ZL manufactured by Nissan Kagaku.
(Silica anhydride 40% by weight, average particle diameter 90 nm), and Nissan Chemical's Snowtex 30 (silicic acid anhydride 30% by weight, average particle diameter 30 nm) were used. The test method of the mold is Japanese Industrial Standards "Gypsum-based investment material for dental casting" T6601.
-1998. That is, the curing time and the compressive strength complied with this, and the thermal expansion was raised to 800 ° C., and the numerical values were read. Mixing method for investment materials is 2
Snowtex ZL was made into a kneading liquid A and Snowtex 30 was made into a kneading liquid B with 2 mL / 100 g of powder. A Matsukaze power lift mixer was used as the vacuum stirrer, and the kneading time was 30 seconds.
【0040】硬化膨張の試験
リング径高さ40mm、内径40mmのリングに松風ノ
ンアスベストを内張りしてワセリン塗布した。リングに
練和泥を流し込み、ガラス板を載せ、縦型ダイヤルゲー
ジ(1/100mm読みとり)にて硬化膨張値を読みと
り、膨張率を計算する。総合膨張とは、熱膨張に硬化膨
張を加えた膨張量のことである。Curing expansion test ring A ring having a diameter of 40 mm and an inner diameter of 40 mm was lined with Matsukaze non-asbestos and applied with vaseline. The kneading mud is poured into the ring, a glass plate is placed on the ring, the hardening expansion value is read with a vertical dial gauge (1/100 mm reading), and the expansion coefficient is calculated. The total expansion is an expansion amount obtained by adding hardening expansion to thermal expansion.
【0041】ヒートショック試験
リング径高さ55mm、内径40mmのリングに松風ノ
ンアスベストを内張りしてワセリン塗布した。リングに
練和泥を流し込み、練和開始から20分後に800℃に
昇温したファーネスに入れ、クラックの発生を確認し
た。鋳造不可能な場合は×とし、クラックが発生してい
るものは△とし、全くクラックが無いものは○とした。Heat Shock Test Ring A ring having a diameter height of 55 mm and an inner diameter of 40 mm was lined with Matsukaze non-asbestos and applied with vaseline. The kneaded mud was poured into the ring, and 20 minutes after the kneading was started, the kneaded mud was put into a furnace heated to 800 ° C., and cracking was confirmed. When casting was impossible, it was marked with X, when cracks were found, it was marked with Δ, and when there were no cracks, it was marked with ◯.
【0042】鋳造面の確認
リング径高さ55mm、内径40mmのリングに松風ノ
ンアスベストを内張りしてワセリン塗布した。リングに
練和泥を流し込み、練和開始から20分後に800℃に
昇温したファーネスに入れ、30分係留後、松風ユニメ
タルを鋳造し、その表面性状を確認した。表面研磨の必
要のないものを○とし、表面を研磨して使用可能なもの
を△とし、鋳造体表面に著しい突起物がある場合を×と
した。Confirmation of Cast Surface A ring having a ring diameter of 55 mm and an inner diameter of 40 mm was lined with Matsukaze non-asbestos and coated with vaseline. The kneaded mud was poured into the ring, and 20 minutes after the kneading was started, the kneaded mud was put into a furnace heated to 800 ° C., and after 30 minutes of mooring, Matsukaze unimetal was cast, and its surface properties were confirmed. Those that did not require surface polishing were marked with ◯, those that could be used after polishing the surface were marked with Δ, and those with significant protrusions on the surface of the casting were marked with x.
【0043】[0043]
【表4】 [Table 4]
【0044】[0044]
【効果】上記結果のように、本発明により、プレシャス
合金からノンプレシャス合金まで幅広く鋳造でき、表面
性状がよく、急速加熱を行ってもヒートショックに強
く、亀裂やクラックが入ることがない歯科用急速加熱型
リン酸塩系埋没材を得ることができた。[Effects] As described above, according to the present invention, it is possible to cast a wide range of materials from precious alloys to non-precious alloys, has good surface properties, is resistant to heat shock even when subjected to rapid heating, and is free from cracks and cracks. A rapid heating type phosphate investment material could be obtained.
【0045】本発明により、リン酸塩系埋没材におい
て、表面性状を向上させ、十分な硬化膨張を得られ、な
おかつ急速加熱をしても亀裂やクラックのないヒートシ
ョックに強い歯科用急速加熱型リン酸塩系埋没材を得る
ことができた。本発明は、精密な鋳造体を短時間で鋳造
でき、ヒートショックに強く、大きな総合膨張を得るこ
とにより幅広い金属に使用でき、表面性状が滑沢な鋳造
体を得ることができる埋没材を創製することである。ま
た、本発明を利用することにより、鋳造時には十分な圧
縮強度を有し、鋳造体を掘り出しやすいものが得られ
た。According to the present invention, in a phosphate-based investment material, a rapid heating type for dental use, which has improved surface properties, sufficient curing expansion, and is resistant to heat shock without cracks or cracks even when rapidly heated. A phosphate-based investment material could be obtained. The present invention creates an investment material that can cast a precision casting in a short time, is resistant to heat shock, can be used for a wide range of metals by obtaining a large total expansion, and can obtain a casting with smooth surface properties. It is to be. Further, by utilizing the present invention, a product having sufficient compressive strength during casting and easily digging out a cast body was obtained.
Claims (4)
グネシウム、(b)第1リン酸アンモニウム、(c)骨
材を含むリン酸塩系埋没材において、(a)平均粒径が
10〜40μmである酸化マグネシウム(b)第1リン
酸アンモニウムのうち、25μm以下が全第1リン酸ア
ンモニウムに対して10〜45重量%であることを特徴
とする歯科用急速加熱型リン酸塩系埋没材。1. An investment material for dental casting, comprising: (a) magnesium oxide, (b) ammonium phosphate monobasic, and (c) a phosphate-based investment material containing aggregate, wherein (a) average particle size. Of 10 to 40 μm of magnesium oxide (b) monobasic ammonium phosphate, 25 μm or less is 10 to 45% by weight based on the total ammonium monobasic phosphate, dental rapid heating phosphoric acid Salt-based investment material.
系埋没材であって、(a)酸化マグネシウムが5〜15
重量%(b)第1リン酸アンモニウム10〜20重量%
であることを特徴とする歯科用急速加熱型リン酸塩系埋
没材。2. The dental rapid heating phosphate-based investment material according to claim 1, wherein (a) magnesium oxide is 5 to 15.
% By weight (b) 10 to 20% by weight of primary ammonium phosphate
A rapid heating type phosphate-based investment material for dentistry.
酸塩系埋没材であって(c)骨材がジルコニア、ケイ酸
ジルコニウム、溶融石英、ムライト、アルミナから選ば
れた1種以上を含むことを特徴とする歯科用急速加熱型
リン酸塩系埋没材。3. The dental rapid heating type phosphate-based investment material according to claim 1, wherein the aggregate (c) is one selected from zirconia, zirconium silicate, fused silica, mullite and alumina. A rapid-heating dental phosphate-based investment material for dental use, which comprises the above.
酸塩系埋没材を練和する専用液としてコロイダルシリカ
溶液を用い、そのコロイダルシリカの平均粒径が70〜
100nmである歯科用急速加熱型リン酸塩系埋没材。4. A colloidal silica solution is used as a dedicated liquid for kneading the rapid-heating dental phosphate-based investment material according to any one of claims 1 to 3, and the average particle diameter of the colloidal silica is 70 to 70.
Dental rapid heating phosphate-based investment material with a thickness of 100 nm.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001253636A JP4786080B2 (en) | 2001-07-19 | 2001-07-19 | Dental rapid heating phosphate investment |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001253636A JP4786080B2 (en) | 2001-07-19 | 2001-07-19 | Dental rapid heating phosphate investment |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2003034608A true JP2003034608A (en) | 2003-02-07 |
| JP4786080B2 JP4786080B2 (en) | 2011-10-05 |
Family
ID=19081929
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001253636A Expired - Lifetime JP4786080B2 (en) | 2001-07-19 | 2001-07-19 | Dental rapid heating phosphate investment |
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| Country | Link |
|---|---|
| JP (1) | JP4786080B2 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20150018888A (en) | 2012-06-18 | 2015-02-24 | 요시노 셋고 가부시키가이샤 | Casting investment composition and casting process using same |
| US9834480B2 (en) | 2012-04-27 | 2017-12-05 | Yoshino Gypsum Co., Ltd. | Gypsum-based embedding material composition for casting |
| EP3403639A2 (en) | 2017-05-17 | 2018-11-21 | Shofu Inc. | Phosphate-based dental investment material |
| CN115624494A (en) * | 2022-03-31 | 2023-01-20 | 沈阳建筑大学 | Preparation method of dental phosphate embedding material, embedding material and application |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS50111890A (en) * | 1974-02-12 | 1975-09-02 | ||
| JPH06234612A (en) * | 1993-02-09 | 1994-08-23 | Taisei Shika Kogyo Kk | Mold material for dental use |
| JPH0812415A (en) * | 1994-06-24 | 1996-01-16 | Taisei Shika Kogyo Kk | Dental refractory mold material |
-
2001
- 2001-07-19 JP JP2001253636A patent/JP4786080B2/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS50111890A (en) * | 1974-02-12 | 1975-09-02 | ||
| JPH06234612A (en) * | 1993-02-09 | 1994-08-23 | Taisei Shika Kogyo Kk | Mold material for dental use |
| JPH0812415A (en) * | 1994-06-24 | 1996-01-16 | Taisei Shika Kogyo Kk | Dental refractory mold material |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9834480B2 (en) | 2012-04-27 | 2017-12-05 | Yoshino Gypsum Co., Ltd. | Gypsum-based embedding material composition for casting |
| KR20150018888A (en) | 2012-06-18 | 2015-02-24 | 요시노 셋고 가부시키가이샤 | Casting investment composition and casting process using same |
| US9718121B2 (en) | 2012-06-18 | 2017-08-01 | Yoshino Gypsum Co., Ltd. | Casting investment composition and casting process using same |
| EP3403639A2 (en) | 2017-05-17 | 2018-11-21 | Shofu Inc. | Phosphate-based dental investment material |
| JP2018193320A (en) * | 2017-05-17 | 2018-12-06 | 株式会社松風 | Dental phosphate-based buried material |
| US10945927B2 (en) | 2017-05-17 | 2021-03-16 | Shofu Inc. | Phosphate-based dental investment material |
| CN115624494A (en) * | 2022-03-31 | 2023-01-20 | 沈阳建筑大学 | Preparation method of dental phosphate embedding material, embedding material and application |
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| Publication number | Publication date |
|---|---|
| JP4786080B2 (en) | 2011-10-05 |
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