JPS62298350A - Production of calcium phosphate crystallized glass tooth crown - Google Patents
Production of calcium phosphate crystallized glass tooth crownInfo
- Publication number
- JPS62298350A JPS62298350A JP61141443A JP14144386A JPS62298350A JP S62298350 A JPS62298350 A JP S62298350A JP 61141443 A JP61141443 A JP 61141443A JP 14144386 A JP14144386 A JP 14144386A JP S62298350 A JPS62298350 A JP S62298350A
- Authority
- JP
- Japan
- Prior art keywords
- glass
- calcium phosphate
- abutment
- crown
- tooth
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000011521 glass Substances 0.000 title claims description 37
- 239000001506 calcium phosphate Substances 0.000 title claims description 11
- 229910000389 calcium phosphate Inorganic materials 0.000 title claims description 11
- 235000011010 calcium phosphates Nutrition 0.000 title claims description 11
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 title claims description 11
- 210000000332 tooth crown Anatomy 0.000 title claims description 9
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 238000002425 crystallisation Methods 0.000 claims description 14
- 230000008025 crystallization Effects 0.000 claims description 14
- 239000011575 calcium Substances 0.000 claims description 5
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 2
- 239000010440 gypsum Substances 0.000 claims 2
- 229910052602 gypsum Inorganic materials 0.000 claims 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims 1
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 claims 1
- GVALZJMUIHGIMD-UHFFFAOYSA-H magnesium phosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GVALZJMUIHGIMD-UHFFFAOYSA-H 0.000 claims 1
- 239000004137 magnesium phosphate Substances 0.000 claims 1
- 229910000157 magnesium phosphate Inorganic materials 0.000 claims 1
- 229960002261 magnesium phosphate Drugs 0.000 claims 1
- 235000010994 magnesium phosphates Nutrition 0.000 claims 1
- 239000002694 phosphate binding agent Substances 0.000 claims 1
- 239000000377 silicon dioxide Substances 0.000 claims 1
- 229910052845 zircon Inorganic materials 0.000 claims 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 claims 1
- 239000000463 material Substances 0.000 description 20
- 238000000034 method Methods 0.000 description 13
- 239000001993 wax Substances 0.000 description 11
- 238000005266 casting Methods 0.000 description 8
- 239000004575 stone Substances 0.000 description 7
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 239000011574 phosphorus Substances 0.000 description 4
- 239000002002 slurry Substances 0.000 description 4
- 229910019142 PO4 Inorganic materials 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 239000011819 refractory material Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 238000009750 centrifugal casting Methods 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 230000002093 peripheral effect Effects 0.000 description 2
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 206010011878 Deafness Diseases 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 238000009933 burial Methods 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 208000002925 dental caries Diseases 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000001035 drying Methods 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
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 210000000214 mouth Anatomy 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 238000007517 polishing process Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000005488 sandblasting Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000004017 vitrification Methods 0.000 description 1
Landscapes
- Dental Prosthetics (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
3、発明の詳細な説明
(腫業上の利用分野)
本発明はリン酸カルシウム系結晶化ガラス歯冠の製造方
法、特に変形のない高精度の結晶化ガラス歯冠を得る方
法に係るものである。Detailed Description of the Invention 3. Detailed Description of the Invention (Field of Tumor Application) The present invention provides a method for manufacturing a calcium phosphate-based crystallized glass dental crown, and in particular provides a highly accurate crystallized glass dental crown without deformation. It is related to the method.
(従来の技術)
近年歯の欠損部を補う材料としてリン酸カルシウム系ガ
ラスを渦造成形した仮、結晶化する方法により天然歯に
類似した外貌を待ち、硬度や熱伝導度等の特性も天然肉
に近いものを得ることが提案されている。(Conventional technology) In recent years, calcium phosphate glass has been used as a material to fill in tooth defects by swirl-forming and crystallizing it to create an appearance similar to that of natural teeth, and properties such as hardness and thermal conductivity that are similar to those of natural meat. It is suggested to get something close.
この方法は従来の金、l14鋳造の場合と同僚に1、愚
者から取りな支台H!俣型の上で成形したワックスパタ
ーンをもとに遠心鋳造法によりガラスの成形を行うこと
がoT能である。しかし、このままではガラスは透明で
天然歯と外表上の相異があり、又脆く且波折した場合に
鋭い破口が形成されて口腔内を傷つける虞れがあるので
好ましくない。This method is for traditional gold, l14 casting and colleague 1, take it from the fool H! OT technology involves forming glass using a centrifugal casting method based on a wax pattern formed on a mold. However, as it is, glass is not preferable because it is transparent and has a different external surface from natural teeth, and is also brittle and, when broken, may form a sharp break and cause damage to the inside of the oral cavity.
そこで所定の温度迄加熱して結晶化を行ない、結晶化ガ
ラスとすることによシこれらの欠点を防止することが出
来る。Therefore, these defects can be prevented by heating to a predetermined temperature to effect crystallization to obtain crystallized glass.
M晶化の方法は、′A型の中でそのまま行なう手段と、
鋳型から取り出して行なう手段がある。The method of M crystallization is to perform it as it is in the 'A type,
There is a way to remove it from the mold.
(発明の解決しようとする問題点)
しかしながら、前者の手段にあっては鋳型材料とガラス
が鋳造時に反応して固着するため結晶化石垣のときに型
とガラス間に機械的応力が生じ、それが結晶化ガラスに
残留応力を発生させて機械的強度を劣化させたり、歯冠
の変形を起したりする。又、結晶核の生成が不均一とな
り、均質を結晶化ガラスが得遣かったり、湯道の部分が
歯冠部に着いた状態で結晶化を行なう為、歯冠我面にd
I通の痕跡が残る等の問題点がある。(Problem to be solved by the invention) However, in the former method, the mold material and the glass react and stick together during casting, so mechanical stress is generated between the mold and the glass when forming a crystalline stone wall. This generates residual stress in the crystallized glass, deteriorating its mechanical strength and causing deformation of the tooth crown. In addition, the generation of crystal nuclei becomes uneven, and crystallized glass is preferable for homogeneity, and crystallization is performed with the runner part attached to the crown of the tooth.
There are problems such as traces of I-mail remaining.
他方、後者の手段においては、前述の様な問題点は生じ
ないものの、結晶化時にガラスが軟化し、自重による変
形や六回張力により周縁部が丸く変形する。歯冠材料の
場合、周縁部は歯質を削除した部分を封鎖して二次カリ
エスを防ぐ!IK床で特に寸法精度を要求される部分で
あり、この部分の変形は重要な問題でるる。On the other hand, in the latter method, although the above-mentioned problems do not occur, the glass softens during crystallization, and the peripheral edge becomes rounded due to deformation due to its own weight and six-fold tension. In the case of dental crown materials, the periphery seals off the area where tooth structure has been removed to prevent secondary caries! This is the part of the IK floor that requires particularly high dimensional accuracy, and deformation of this part poses an important problem.
(問題点を′S決するための手段)
本発明者は、成形されたガラスを鋳型から取り出して結
晶化を行なうに冷し、冥質的に変形を生ずることなく、
寸法精度の高い状態を保持する手段を見出すことを目的
として槌々研究、検討した結果、特定の支持台を用いて
結晶化を行なうことにより前記目的を達成し得ることを
見出した。(Means for resolving the problem) The present inventor took the molded glass out of the mold and cooled it to the point where it crystallized, without causing any substantive deformation.
As a result of extensive research and examination with the aim of finding a means to maintain a state with high dimensional accuracy, it was discovered that the above object could be achieved by performing crystallization using a specific support stand.
かくして本発明は、歯冠の形状に鋳造成形したリン酸カ
ルシウム系ガラスの内面を、支台歯の形状をしたs o
o ’a以下の温度で変形しない耐火物の外面に密着
するように鉄層して結晶化を行なうことを特徴とするリ
ン酸カルシウム系、結晶化ガラス歯冠の製造方法を提供
するにある。Thus, in the present invention, the inner surface of calcium phosphate glass cast in the shape of a tooth crown is used as an abutment tooth shaped so.
To provide a method for manufacturing a calcium phosphate-based crystallized glass dental crown, which is characterized in that crystallization is performed by forming an iron layer so as to be in close contact with the outer surface of a refractory that does not deform at temperatures below o'a.
本発明に用いられるリン酸カルシウム系ガラスとしては
、リン酸カルシウム質を70重量−以上含有し、リンに
対するカルシウムの原子比Ca/Pが0.35〜0.7
の範囲にあるものは適度な溶融畠度と鋳造が容易なd液
粘性を有し1局い機械的強度と化学昨耐久性を有し、且
天然歯に近似した外観及び硬度を示すので好ましい。The calcium phosphate glass used in the present invention contains at least 70 parts by weight of calcium phosphate, and has an atomic ratio of calcium to phosphorus, Ca/P, of 0.35 to 0.7.
Those within this range are preferable because they have appropriate melt hardness and d liquid viscosity that makes casting easy, have mechanical strength and chemical durability, and exhibit an appearance and hardness similar to natural teeth. .
Ca/Pが0.7を超えるとガラス化が困4となり、逆
に0.35に満たない場合には均一な結晶化が起りにく
くなるのみならず、リン成分が過剰となり、耐久性が低
下するので1c’lれも好ましくない。If Ca/P exceeds 0.7, vitrification will be difficult, while if it is less than 0.35, not only will uniform crystallization be difficult to occur, but the phosphorus component will be excessive and durability will decrease. Therefore, 1c'l is not preferable either.
本発明においては、先づガラス浴l@智を歯科用金属材
料の崎遺用MWに金属材料の鋳造と同様に鋳造成形され
る。即ち、先づ形成した支台歯から印象を採取し、これ
をもとに石膏で支台歯の模型を作成する。In the present invention, first, a glass bath is cast into a metal MW for dental use in the same manner as casting a metal material. That is, an impression is first taken from the formed abutment tooth, and based on this, a model of the abutment tooth is created using plaster.
次に、この石積模型の上にパラフィンワックスな歯冠の
形状に盛り上げて聾を作る。Next, on top of this stone masonry model, we build up paraffin wax in the shape of a tooth crown to create a deaf ear.
こノ型に円柱状パラフィンワックスを用いて湯道を設け
、周dにスラリー状の埋没材を注入する。埋没材の硬化
後、500〜800°Cで熱処理してワックスを焼却し
、−運用の型を作成する。かかる埋没材はスラリー状、
侭から乾燥f化学反応に工り硬化し、しかもその硬化体
が500〜800℃の温度で鋳造成形を行なっても崩癲
しない強度を有するものであればよく、例えばリン酸塩
糸、エチルシリケート系、石・は系等が用いI−)t″
Lる。鋳造は、咳剖型を500〜800℃に保持し、浴
融したガラスを遠心鋳造法、圧迫調造法、真窒圧迫鋳造
法等の方法が法用される。崎這麦、ガラスは鋳型内に入
れたまま急冷を避けなから盟温迄冷却される。A runner is provided in this mold using cylindrical paraffin wax, and a slurry-like investment material is injected around the periphery d. After the investment material has hardened, it is heat treated at 500 to 800°C to burn off the wax and create an operational mold. This investment material is in the form of a slurry,
Any material can be used as long as it is hardened by drying through a chemical reaction and the hardened product has a strength that does not collapse even when cast at a temperature of 500 to 800°C, such as phosphate thread, ethyl silicate, etc. I-)t''
L. For casting, methods such as the centrifugal casting method, compression conditioning method, true nitrogen compression casting method, etc. are used to maintain the mold at 500 to 800° C. and melt the glass in a bath. The glass is kept in the mold and cooled down to the temperature required to avoid rapid cooling.
埋没材からのガラスの取り出しは、爾科技工用ドリルや
ビンセット等を用いて行なわれるが、結鵡化前のガラス
はかなり脆いのでガラスビーズを4に9/−程度の圧力
で吹きつけるサンドブラスト法を用いるのが好ましい。Glass is removed from the investment material using a technical drill or a bottle set, but since glass before it hardens is quite brittle, sandblasting, in which glass beads are blown at a pressure of about 4 to 9, is used. Preferably, the method is used.
。.
久いでガラスの゛産道部分を切断し、−短形状を藍える
。しかし、所望によシ湯道は切断しなくてもよい。After a while, I cut the birth canal part of the glass and dyed it into a rectangular shape. However, the runners may not be cut if desired.
成形されたガラスはその内面が支台歯の形状をした耐火
物の外面に街着するように被せることにより、変形を防
ぎながらR6化せしめる。The molded glass is placed on the outside of the refractory whose inner surface is in the shape of an abutment tooth, thereby preventing deformation and making it R6.
かかる;耐火物としては、支台Aの形状に成形可能で且
s o o ’o以下で安定なものであれば舟に制限は
ないが、支台歯の形状に成形が容易な鋳造用埋没材が′
4に好ましく、例えばリン酸塩系埋没材、エチルシリケ
ート糸埋没材、石′薩系4没材等が挙げられる。又支台
歯保型用の硬質石骨も好適である。There is no restriction on the refractory material as long as it can be molded into the shape of the abutment A and is stable at less than s o o 'o, but there are no restrictions on the refractory material, but there are no restrictions on the refractory material, as long as it can be molded into the shape of the abutment A and is stable at less than s o o 'o. The material is
Preferred examples include phosphate-based investment materials, ethyl silicate thread investment materials, and stone-based investment materials. Hard stone bone for the abutment tooth retainer is also suitable.
本発明に用いられる債晶化用支台の作成は、例えば以下
の様に行なわれる。The preparation of the abutment for debt crystallization used in the present invention is performed, for example, as follows.
先づ支台歯の印求を課者から直接、或は石材作業模型か
ら床る。First, the impression of the abutment tooth is made directly from the imprinter or from the stone working model.
印未材としては1.患者から直接印象する場合には通常
のアルギン酸4糸、ラバー系、寒天系等が、又石ヰ模型
から印象する場合には上記印象材も用い得るが、鋳造用
ワックスを用いると印tUから結晶化用支台な取り外す
のにワックスを焼却するだけで済むので特に好ましい。1. When making an impression directly from the patient, ordinary alginate 4 threads, rubber type, agar type, etc. can be used, and when making an impression from a stone model, the above impression materials can be used, but when casting wax is used, crystals from the mark tU can be used. This is particularly preferred since the wax can be removed by simply burning off the wax.
かくして得た印象に、耐火物スラリーを流し込み硬化せ
しめる。耐火物スラリーの硬化後、印象型から支台な取
り外す。しかし前述の如くワックスで印象型を、採った
場合はこの操作を省くことが出来る。A refractory slurry is poured into the impression thus obtained and allowed to harden. After the refractory slurry has hardened, remove the abutment from the impression mold. However, if an impression mold is made with wax as mentioned above, this operation can be omitted.
そのdk堀&材を処方に従って焼成し、十分な強度を持
たせて支台を形成する。The dk moat & lumber is fired according to the recipe to give it sufficient strength and form the support.
かくして得られた支台にガラス歯冠を披せ、熱処理して
結晶化せしめる。The glass dental crown is placed on the abutment thus obtained and heat treated to crystallize it.
このとき−Ji7cfの内面は支台と接触する為、支台
の表−状態を反映して光沢のない面となるが、内面だけ
なので審美性に何ら影・−を与えず、逆に湊着するとき
の接着強度が制められる利点がある。尚、ガラス歯冠の
成形時に用いた埋没材を全て外すことなく、歯冠の内側
の埋没材を安し、これを支台耐大物として用いることも
出来、本発明はかかる悪J5Rをも含むものである。−
他方、(至)冠の外面は結晶化時のガラスの軟化に伜な
い、表面う長刀lこより囃めて光沢のある平滑な表面と
なり、通常行なわれる研帽、艶出しの工程が省略出来る
利点がある。At this time, since the inner surface of Ji7cf comes into contact with the abutment, it becomes a matte surface reflecting the surface condition of the abutment, but since it is only the inner surface, it does not affect the aesthetics at all; This has the advantage of controlling the adhesive strength when bonding. Incidentally, without removing all the investment material used when molding the glass crown, the investment material inside the crown can be made cheap and used as a large abutment, and the present invention also includes such a bad J5R. It is something that −
On the other hand, the outer surface of the crown has the advantage that it does not soften the glass during crystallization and has a smooth, glossy surface due to the surface elongation, which eliminates the usual grinding and polishing processes. There is.
(実施列)
実m互12す1
支台歯の石・q作業模型からワックスパターンをと9、
これをリン酸塩系埋没材(偲山コ違社製ブルーペスト)
K埋没後、a o o ’o迄加熱してワックスを焼却
して鋳型を作成した。次にこの型に1300’Oで加、
4PR@aしたCI!L025重量%、P2O574劃
0、ム12031g量−の組成を有するリンはカルシウ
ム系ガラスを遠心A造した。(Implementation row) Actual m 12 s 1 A wax pattern is drawn from the abutment tooth stone q work model and 9.
Use this as a phosphate-based investment material (Blue Pest, manufactured by Keishan Kowaisha).
After K burial, the wax was burnt off by heating to ao o 'o to create a mold. Next, add 1300'O to this mold,
4PR@a CI! Phosphorus having a composition of 25% by weight of L0, 574% of P2O, and 12031g of phosphorus was prepared by centrifugation A of calcium-based glass.
これを鋳型ごと500 ’Oに保った電気炉に入れ、1
時間保持した麦、50’O/時の速度で室温迄冷却した
。This was placed together with the mold in an electric furnace maintained at 500'O, and
The barley was kept for a period of time and cooled to room temperature at a rate of 50'O/hr.
次いでガラスピーズな4に9/−の圧力で吹きつけ、前
記ガラス員造体を埋没材から取り出した。そして湯道部
を切断し、グラインダーで形を整え、パリや突起、気泡
の巻き込みのないことを確認した。Next, it was blown onto glass beads 4 at a pressure of 9/-, and the glass member structure was taken out from the investment material. The runner was then cut and shaped using a grinder, making sure that there were no cracks, protrusions, or air bubbles.
次に、ワックスパターン作成時に使用した作業模型の支
台歯にワックスを盛り上げ、支台歯の型を取り、これに
シリカの骨材にリン酸マグネ7ウムの結合材を配合した
耐火物(徳山d遍社製ブルーペスト)のスラリーを流し
込み、硬化m800’o迄加熱してワックスを・焼却し
、結晶化用支台を得た。Next, wax was applied to the abutment teeth of the working model used to create the wax pattern, a mold was taken of the abutment teeth, and a refractory (Tokuyama A slurry of Blue Pesto (manufactured by d Hensha) was poured in and heated to a hardening temperature of 800'o to incinerate the wax to obtain a support for crystallization.
これに前述のガラス歯冠を、その円囲が支台の外題にt
i層する工つに被せて電気炉に入れ、3oO℃/時の速
度で700℃迄昇温し、その温匿に4時間保持して結晶
化を行なった。結晶化後、歯冠は支台から容易に取り外
せた。The above-mentioned glass tooth crown is attached to this, and its circumference is the outer diameter of the abutment.
The material was placed over the i-layer and placed in an electric furnace, heated to 700° C. at a rate of 300° C./hour, and kept at that temperature for 4 hours to effect crystallization. After crystallization, the crown was easily removed from the abutment.
借られた歯冠は均一に結晶化して分り、外観上のムラは
認められず、又外面は平1′#で5F若の必要Vユなか
った。又内@は支普我lとの接触で光沢はなかったが、
大@な凹凸riなかった。The borrowed tooth crown was found to be uniformly crystallized, no unevenness was observed in appearance, and the outer surface was flat 1'# and did not have the necessary V-shape of 5F. Matauchi @ was not shiny due to contact with Shifuga l,
There were no major irregularities.
歯冠の周縁部の最大直径を測定して元の模型からの寸法
変化を測定した績釆を辰1に示し之。衣lには支台ば模
型に歯冠を被せたときの適合性及び外表の様子も併せて
示した。The results of measuring the maximum diameter of the peripheral part of the tooth crown and measuring the dimensional change from the original model are shown in Figure 1. Clothes 1 also shows the compatibility and external appearance when the crown is placed on the abutment model.
実施例2〜7
実施例1と同様にして成形したガラスを、櫨々の支台用
耐火物上で実施例1と同様に結晶化を行なった。Examples 2 to 7 Glass molded in the same manner as in Example 1 was crystallized in the same manner as in Example 1 on a refractory for an abutment.
結晶化後の歯冠について夫々周縁部の最大直径の寸法変
化、支台歯の模型に対する適合性、外殼を夫々戒1に示
した。Regarding the crowns after crystallization, dimensional changes in the maximum diameter of the periphery, compatibility with the abutment tooth model, and outer shell are shown in Precept 1.
比較例
実施例1と同様に鋳造成形したガラスを埋没材から堀り
出した麦、平らな耐火物上にのせて実施例1と同様の熱
処理を行なった。Comparative Example A glass molded by casting in the same manner as in Example 1 was placed on a flat refractory made of wheat excavated from the investment material, and heat treated in the same manner as in Example 1.
得られた結晶化ガラスは均一で平滑な表面が得られたが
、形状は全く変形してしまい、元の石積模型に適合させ
ることは不可能であった。Although the obtained crystallized glass had a uniform and smooth surface, the shape was completely deformed and it was impossible to fit it into the original masonry model.
これについても物性を表1に示した。The physical properties of this material are also shown in Table 1.
Claims (1)
スの内面を、支台歯の形状をした800℃以下の温度で
変形しない耐火物の外面に密着するように装着して結晶
化を行なうことを特徴とするリン酸カルシウム系結晶化
ガラス歯冠の製造方法。 2、耐火物は石膏系、エチルシリケート系、リン酸マグ
ネシウム系、リン酸アルミニウムの結合材により、シリ
カ、アルミナ、ジルコンの骨材を結合したもの或は硬質
石膏である請求の範囲(1)の製造方法。 3、リン酸カルシウム系ガラスは、リン酸カルシウム質
を70重量%以上含有し、Ca/Pの原子比が0.35
〜0.7の組成を有する請求の範囲(1)の製造方法。[Claims] 1. The inner surface of calcium phosphate glass cast in the shape of a tooth crown is attached so as to be in close contact with the outer surface of a refractory that is shaped like an abutment tooth and does not deform at temperatures below 800°C. A method for producing a calcium phosphate-based crystallized glass tooth crown, which comprises performing crystallization. 2. The refractory is one in which aggregates of silica, alumina, and zircon are bound by a gypsum-based, ethyl silicate-based, magnesium phosphate-based, or aluminum phosphate binder, or hard gypsum. Production method. 3. Calcium phosphate glass contains 70% by weight or more of calcium phosphate and has a Ca/P atomic ratio of 0.35.
The manufacturing method according to claim (1), having a composition of ˜0.7.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61141443A JPS62298350A (en) | 1986-06-19 | 1986-06-19 | Production of calcium phosphate crystallized glass tooth crown |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61141443A JPS62298350A (en) | 1986-06-19 | 1986-06-19 | Production of calcium phosphate crystallized glass tooth crown |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62298350A true JPS62298350A (en) | 1987-12-25 |
Family
ID=15292055
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61141443A Pending JPS62298350A (en) | 1986-06-19 | 1986-06-19 | Production of calcium phosphate crystallized glass tooth crown |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62298350A (en) |
-
1986
- 1986-06-19 JP JP61141443A patent/JPS62298350A/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6400748B2 (en) | Dental restoration material, method for producing the same, and ingot | |
DE69529037D1 (en) | Impregnated ceramic network for the production of dental molds and restorations | |
JPH0234615B2 (en) | ||
JP3389212B2 (en) | Method for manufacturing dental investment material and dental mold | |
JPS6287427A (en) | Mold material | |
JPS62298350A (en) | Production of calcium phosphate crystallized glass tooth crown | |
JPH0193439A (en) | Production of crystallized glass for dental material and embedding material | |
WO2013109491A1 (en) | Investment composition material having a reducing agent | |
US2195452A (en) | Method of making articles of porcelain | |
US4662924A (en) | Method for molding calcium phosphate type glass | |
JP3193555B2 (en) | Manufacturing method of glass ceramic crown | |
US2341998A (en) | All ceramic denture and method of producing same | |
US3234607A (en) | Method of forming an investment mold with potassium sulfate additive | |
JP4288491B2 (en) | Recycling method of dental casting investment | |
CN106798598A (en) | Base plate wax application process in oral cavity is fixed and repaired | |
JP3677760B2 (en) | Manufacturing method of ceramic crown | |
JPH04330006A (en) | Dental investment and mold for dental investment | |
JPH0787848B2 (en) | Mold for molding | |
JPS6187543A (en) | Production of dental cast product | |
CN1278798C (en) | Special investment for oral cast titanium and its shaping preparation method | |
JPS59166340A (en) | Casting method of titanium product | |
JPS63310737A (en) | Mold material for molding | |
JPS61147943A (en) | Hardener liquid of molding material for dental purpose | |
JPS60131835A (en) | Manufacture of calcium phosphate cast body | |
JP2725027B2 (en) | Embedding material for calcium phosphate glass crystallization |