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JPH06687B2 - Denture base molding material - Google Patents

Denture base molding material

Info

Publication number
JPH06687B2
JPH06687B2 JP61182646A JP18264686A JPH06687B2 JP H06687 B2 JPH06687 B2 JP H06687B2 JP 61182646 A JP61182646 A JP 61182646A JP 18264686 A JP18264686 A JP 18264686A JP H06687 B2 JPH06687 B2 JP H06687B2
Authority
JP
Japan
Prior art keywords
denture base
mold
weight
gypsum
calcium carbonate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP61182646A
Other languages
Japanese (ja)
Other versions
JPS6339806A (en
Inventor
嘉宏 斉藤
雅樹 田村
充也 坂本
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.)
Ube Corp
Original Assignee
Ube Industries Ltd
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 Ube Industries Ltd filed Critical Ube Industries Ltd
Priority to JP61182646A priority Critical patent/JPH06687B2/en
Publication of JPS6339806A publication Critical patent/JPS6339806A/en
Publication of JPH06687B2 publication Critical patent/JPH06687B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

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  • Curing Cements, Concrete, And Artificial Stone (AREA)
  • Dental Preparations (AREA)

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、熱可塑性樹脂を用いて義歯床を成形する際の
成形型に関する。
TECHNICAL FIELD The present invention relates to a molding die for molding a denture base using a thermoplastic resin.

[従来技術およびその問題点] 従来、義歯床はアクリルポリマー製のものが多い。これ
はアクリルモノマーとポリマーとの混合物を、石膏型内
で室温あるいは比較的低温に加熱し、重合させることに
より形成される。
[Prior Art and its Problems] Conventionally, most denture bases are made of acrylic polymer. It is formed by heating a mixture of an acrylic monomer and a polymer in a gypsum mold at room temperature or a relatively low temperature to polymerize the mixture.

熱可塑性樹脂を用いて義歯床を圧縮成形する際には、成
形型内で樹脂を軟化変形させるため、成形型を200〜
350℃にも昇温する必要がある。この昇温により石膏
型の圧縮強度が大きく低下し、成形圧に耐えられなくな
り損壊する。さらに、結晶水を失なって激しく収縮する
ため、義歯床の口腔印象への適合性が不良となる。
When a denture base is compression-molded using a thermoplastic resin, in order to soften and deform the resin in the molding die,
It is necessary to raise the temperature to 350 ° C. Due to this temperature rise, the compressive strength of the gypsum mold is greatly reduced, and it cannot withstand the molding pressure and is damaged. Furthermore, since the water of crystallization is lost and the water shrinks violently, the compatibility of the denture base with the oral impression becomes poor.

特開昭59−195561号公報には、石膏と酸化珪素
との混合物からなる成形型が、200〜400℃の加熱
によっても圧縮強度の低下および収縮を生じないことが
開示されている。しかし、酸化珪素としてクリストバラ
イトを使用した場合、このものが250〜300℃の温
度範囲で著しい体膨張を生ずるため、250℃以下で成
形した場合と300℃以上で成形した場合とで型の寸法
が大きく異なる。そのため使用する熱可塑性樹脂の軟化
温度に従って石膏とクリストバライトとの割合を調整す
る必要がある。また、酸化珪素として石英を使用した場
合、その体膨張係数が小さいため、降温時の熱可塑性樹
脂の熱収縮による体積減少を、型の容積膨張が補償し得
ず、義歯床の口腔印象への適合性が不良となる。この場
合、コロイダルシリカの濃度を高め、型の容積膨張を大
とすれば、口腔印象への適合性は改善されるが、加熱に
より型に亀裂が発生するという新たな問題が生ずる。
Japanese Patent Application Laid-Open No. 59-195561 discloses that a mold made of a mixture of gypsum and silicon oxide does not cause reduction in compressive strength and shrinkage even when heated at 200 to 400 ° C. However, when cristobalite is used as the silicon oxide, it causes significant body expansion in the temperature range of 250 to 300 ° C. Therefore, the size of the mold varies depending on whether it is molded at 250 ° C. or lower and at 300 ° C. or higher. to differ greatly. Therefore, it is necessary to adjust the ratio of gypsum and cristobalite according to the softening temperature of the thermoplastic resin used. Further, when quartz is used as the silicon oxide, since its body expansion coefficient is small, the volume expansion of the mold cannot compensate for the volume decrease due to the thermal contraction of the thermoplastic resin at the time of temperature decrease, and the oral impression of the denture base is The compatibility is poor. In this case, if the concentration of colloidal silica is increased and the volume expansion of the mold is increased, the conformity to the oral impression is improved, but there is a new problem that the mold is cracked by heating.

さらに、石膏とクリストバライトとを混合した場合、両
者の比重がかなり異なっているため、振動などにより成
分が分離する場合もある。
Furthermore, when gypsum and cristobalite are mixed, the components may be separated due to vibration or the like because the specific gravities of the two are quite different.

[問題点を解決するための手段] 本発明は、熱可塑性樹脂を用いて、口腔印象への適合性
が優れた義歯床を、容易に成形可能な成形型に関する。
[Means for Solving Problems] The present invention relates to a molding die that can easily mold a denture base excellent in adaptability to an oral impression using a thermoplastic resin.

本発明は、30〜70重量%の石膏と70〜30重量%
の炭酸カルシウムとからなる混合物100重量部に対
し、18〜40重量部のコロイダルシリカが混合された
熱可塑性樹脂製義歯床成形型材料に関する。
The present invention is 30-70 wt% gypsum and 70-30 wt%
The present invention relates to a denture base molding material made of a thermoplastic resin in which 18 to 40 parts by weight of colloidal silica is mixed with 100 parts by weight of a mixture of calcium carbonate.

本発明の成形型は、加熱により過大に収縮することがな
く、また、加熱後も成形圧に耐え得る高い圧縮強度を保
持される。そのため成形が容易で確実であり、得られた
義歯床は口腔印象への適合性が優れている。
The mold of the present invention does not excessively shrink due to heating, and also maintains high compressive strength capable of withstanding the molding pressure even after heating. Therefore, molding is easy and reliable, and the obtained denture base has excellent compatibility with the oral impression.

石膏としては、α型またはβ型結晶構造であって、1/2
分子の結晶水を有しているα型半水石膏あるいはβ型半
水石膏が使用される。
As gypsum, it has an α-type or β-type crystal structure,
Α-type hemihydrate gypsum or β-type hemihydrate gypsum having molecular water of crystallization is used.

α型半水石膏は、石膏の主原料である二水石膏を湿式加
熱することにより得られる。また、β型半水石膏は、二
水石膏を乾式加熱することにより得られる。
The α-type hemihydrate gypsum is obtained by wet-heating gypsum dihydrate, which is the main raw material of gypsum. The β-type hemihydrate gypsum can be obtained by dry heating gypsum dihydrate.

炭酸カルシウムとしては、石灰岩などを粉砕して製造さ
れる重質炭酸カルシウム、石灰乳に二酸化炭素を焼き込
んで製造される軽質炭酸カルシウムなどを使用できる。
炭酸カルシウムの粒径は100μ以下、特に50μ以下
の比較的粒径の小さいものが好ましい。
As the calcium carbonate, heavy calcium carbonate produced by crushing limestone or the like, light calcium carbonate produced by baking lime milk with carbon dioxide, or the like can be used.
The calcium carbonate preferably has a particle size of 100 μm or less, particularly 50 μm or less, and a relatively small particle size.

コロイダルシリカは別名シルカゾルともいわれ、無水珪
素の超微粒子をコロイダル溶液として、利用し易く安定
な状態としたものである。二酸化珪素の含有量は20〜
50重量%のものが一般的である。通常粒径が5〜90
mμ程度の超微粒子であるため、微細な空隙へも容易に
浸透する。外観は透明な乳白色あるいは乳白色のコロイ
ド液である。pHが11.5以上ではゲル化し易く、pH2〜
11で安定であるが、弱酸性の方が取り扱い上好まし
い。中性もしくはアルカリ性では、石膏と二酸化珪素の
混合時に固化し易く操作性に難点がある。
Colloidal silica, which is also called as silcasol, is an ultrafine particle of anhydrous silicon that is used as a colloidal solution in a stable and easy-to-use state. The content of silicon dioxide is 20-
It is generally 50% by weight. Normal particle size is 5 to 90
Since it is an ultrafine particle of about mμ, it easily penetrates into minute voids. Appearance is a transparent milky white or milky white colloidal liquid. If the pH is 11.5 or higher, it easily gels, and
It is stable at 11, but weakly acidic is preferable in terms of handling. If it is neutral or alkaline, it tends to solidify when gypsum and silicon dioxide are mixed, and there is a problem in operability.

石膏と炭酸カルシウムとの組成割合は、石膏30〜70
重量%、炭酸カルシウム70〜30重量%、特に石膏4
0〜70重量%、炭酸カルシウム60〜30重量%であ
ることが好ましい。石膏が30重量%未満である場合
は、型が硬く脆くなり、成形圧により型が破損する。石
膏が70重量%を越える場合は、昇温により型の圧縮強
度が低下し、型が破損する。また、型が激しく収縮し、
義歯床の口腔印象への適合性が不良となる。
The composition ratio of gypsum and calcium carbonate is 30-70 gypsum.
% By weight, 70-30% by weight calcium carbonate, especially gypsum 4
It is preferably 0 to 70% by weight and calcium carbonate 60 to 30% by weight. If the amount of gypsum is less than 30% by weight, the mold becomes hard and brittle, and the mold is damaged by the molding pressure. If the amount of gypsum is more than 70% by weight, the compressive strength of the mold is lowered by the temperature rise and the mold is broken. Also, the mold shrinks violently,
The denture base has poor compatibility with the oral impression.

コロイダルシリカは、上記石膏と炭酸カルシウムとの混
合物100重量部にたいし、18〜40重量部混合され
る。コロイダルシリカの配合量が、18重量部未満では
混合物の粘度が過大であって練和不能であり、40重量
部を越える場合は、義歯床成形型材料の強度が不充分と
なる。
Colloidal silica is mixed in an amount of 18 to 40 parts by weight with respect to 100 parts by weight of the mixture of gypsum and calcium carbonate. If the amount of the colloidal silica is less than 18 parts by weight, the viscosity of the mixture is too high to be kneaded, and if it exceeds 40 parts by weight, the strength of the denture base molding material becomes insufficient.

本発明の材料には、材料本来の強度および熱的特性など
を損なわない範囲で、必要に応じて、硬化時間を調節す
るための促進剤あるいは遅延剤、型に自然な色を与える
ための着色剤などを添加してもよい。
The material of the present invention contains, as necessary, an accelerator or a retarder for adjusting the curing time, and a coloring for giving a natural color to the mold, as long as the original strength and thermal properties of the material are not impaired. Agents and the like may be added.

本発明の材料を得るための方法は、特に限定されるもの
ではなく、通常実施されている震盪法あるいは機械的混
合法などが適用できる。
The method for obtaining the material of the present invention is not particularly limited, and a commonly used shaking method or mechanical mixing method can be applied.

義歯床を成形する熱可塑性樹脂には、 (1)成形時に熱劣化を起こさない。The thermoplastic resin used to mold the denture base has (1) no thermal deterioration during molding.

(2)適度な粘度を有し、賦形性が良好である。(2) It has an appropriate viscosity and good shapeability.

(3)歯肉に近似した色に着色が可能である。(3) It can be colored in a color similar to gingiva.

(4)適度な剛性と耐湿性を有し、使用時の耐環境応力亀
裂性が良好である。
(4) It has appropriate rigidity and moisture resistance, and has good environmental stress crack resistance during use.

などの特性が要求される。Such characteristics are required.

この様な樹脂としては、ポリスチレン、ポリメチルメタ
アクリレート、ポリメチルペンテン−1、ポリアミド、
ポリエステル、ポリカーボネート、ABS樹脂、ポリサ
ルホンなどが挙げられる。特に、ポリサルホン、ポリエ
ーテルサルホンなどのポリサルホン系樹脂が耐湿性、剛
性、耐環境応力亀裂性などが優れていて好ましい。
Such resins include polystyrene, polymethylmethacrylate, polymethylpentene-1, polyamide,
Examples thereof include polyester, polycarbonate, ABS resin, polysulfone and the like. In particular, polysulfone resins such as polysulfone and polyether sulfone are preferable because they have excellent moisture resistance, rigidity, environmental stress crack resistance, and the like.

本発明の義歯床成形型材料は、300℃、1時間以上の
加熱処理を実施しても、200kg/cm2以上の高い圧縮
強度を保持し得る。また、熱可塑性樹脂の熱収縮による
体積減少を補償し得る容積膨張を示す。特に、石膏40
〜70重量%、炭酸カルシウム60〜30重量%の組成
では、コロイダルシリカの濃度に依存して0.4〜0.9%の
容積膨張を示し、150〜350℃の広い温度範囲で0.
07〜0.15%の安定した熱膨張係数を有する。そのた
め、熱可塑性樹脂の加熱軟化条件に影響されない優れた
成形寸法性が得られる。また、本発明の義歯床成形型材
料は、急加熱によっても亀裂を生ずることがなく、形状
安定性および強度の優れた義歯床成形型が得られる。さ
らに、炭酸カルシウムの室温付近での比重は2.71で、
石膏の比重2.75に極めて近いため、振動などによって
成分分離を生ずることなく、均一な型が得られる。
The denture base molding material of the present invention can maintain a high compressive strength of 200 kg / cm 2 or more even if it is subjected to heat treatment at 300 ° C. for 1 hour or more. Further, it shows a volume expansion capable of compensating for the volume decrease due to the thermal contraction of the thermoplastic resin. Especially plaster 40
In the composition of ~ 70 wt% and calcium carbonate of 60-30 wt%, the volume expansion of 0.4-0.9% is shown depending on the concentration of colloidal silica, and in a wide temperature range of 150-350 ° C.
It has a stable coefficient of thermal expansion of 07-0.15%. Therefore, excellent molding dimensional properties that are not affected by the heating and softening conditions of the thermoplastic resin can be obtained. Further, the denture base molding material of the present invention does not cause cracks even by rapid heating, and a denture base molding die having excellent shape stability and strength can be obtained. Furthermore, the specific gravity of calcium carbonate near room temperature is 2.71,
Since the specific gravity of gypsum is very close to 2.75, a uniform mold can be obtained without causing component separation due to vibration.

以下に実施例および比較例によって本発明を詳しく説明
する。
The present invention will be described in detail below with reference to Examples and Comparative Examples.

実施例1 α半水石膏60重量%、重質炭酸カルシウム40重量%
とを機械的に充分混合した後、この混合物100重量部
に対し、20重量部の粉液比0.22のコロイダルシリ
カ液で練和し、ろう義歯の埋没を行い、以下、歯科の通
例に従って義歯成形用の割型を作成した。上下型を乾燥
した後、下型上でポリサルホンを軟化させ、上型を圧着
して義歯床を成形した。冷却後取り出したポリサルホン
義歯床は、口腔印象に忠実であり、型の割れも認められ
なかった。
Example 1 60% by weight of alpha hemihydrate gypsum, 40% by weight of ground calcium carbonate
After mechanically and thoroughly mixing with 100 parts by weight of this mixture, 20 parts by weight of a colloidal silica solution having a powder-liquid ratio of 0.22 was kneaded to embed the wax denture. A split mold for forming a denture was created. After the upper and lower molds were dried, the polysulfone was softened on the lower mold and the upper mold was crimped to form a denture base. The polysulfone denture base taken out after cooling was faithful to the impression of the oral cavity and no mold crack was observed.

実施例2 粉液比0.18のコロイダルシリカ液で練和した他は実施
例1と同様にして義歯床を成形した。
Example 2 A denture base was molded in the same manner as in Example 1 except that the powder was mixed with a colloidal silica liquid having a ratio of 0.18.

得られたポリサルホン義歯床は、口腔印象に忠実であ
り、型の割れも認められなかった。
The obtained polysulfone denture base was faithful to the oral impression, and no mold crack was observed.

比較例1 α半水石膏のみを用いた以外は実施例1と同様にして義
歯床を製造した。得られたポリサルホン義歯床は、型に
割れが生じたことを示しており、また、口腔印象との適
合性が不良であった。
Comparative Example 1 A denture base was manufactured in the same manner as in Example 1 except that only α hemihydrate gypsum was used. The resulting polysulfone denture base showed cracks in the mold and was poorly compatible with the oral impression.

比較例2 α半水石膏40重量%、クリストバライト60重量%を
混合したものを用いた以外は、実施例1と同様にして型
を作成した。下型の温度が220〜250℃の範囲でポ
リカーボネート義歯床を製造したところ、良好な製品が
得られた。しかし、同じ型を用いて下型温度が320℃
になる様にしてポリサルホン義歯床を製造したところ、
口腔印象よりも大きな粘膜面を持つ義歯床が得られ、下
型加熱温度条件による組成調製の必要性が認められた。
Comparative Example 2 A mold was prepared in the same manner as in Example 1 except that 40% by weight of α-hemihydrate gypsum and 60% by weight of cristobalite were used. When a polycarbonate denture base was manufactured at a lower mold temperature of 220 to 250 ° C., a good product was obtained. However, using the same mold, the lower mold temperature was 320 ° C.
When a polysulfone denture base was manufactured as follows,
A denture base with a mucosal surface larger than the oral impression was obtained, and the necessity of composition preparation under lower mold heating temperature conditions was recognized.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】30〜70重量%の石膏と70〜30重量
%の炭酸カルシウムとからなる混合物100重量部に対
し、18〜40重量部のコロイダルシリカが混合された
熱可塑性樹脂製義歯床成形型材料。
1. A thermoplastic resin denture base molding in which 18 to 40 parts by weight of colloidal silica is mixed with 100 parts by weight of a mixture of 30 to 70% by weight of gypsum and 70 to 30% by weight of calcium carbonate. Mold material.
JP61182646A 1986-08-05 1986-08-05 Denture base molding material Expired - Fee Related JPH06687B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61182646A JPH06687B2 (en) 1986-08-05 1986-08-05 Denture base molding material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61182646A JPH06687B2 (en) 1986-08-05 1986-08-05 Denture base molding material

Publications (2)

Publication Number Publication Date
JPS6339806A JPS6339806A (en) 1988-02-20
JPH06687B2 true JPH06687B2 (en) 1994-01-05

Family

ID=16121944

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61182646A Expired - Fee Related JPH06687B2 (en) 1986-08-05 1986-08-05 Denture base molding material

Country Status (1)

Country Link
JP (1) JPH06687B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3389212B2 (en) * 2000-09-14 2003-03-24 株式会社ノリタケカンパニーリミテド Method for manufacturing dental investment material and dental mold

Also Published As

Publication number Publication date
JPS6339806A (en) 1988-02-20

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