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JPH0541585B2 - - Google Patents
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JPH0541585B2 - - Google Patents

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Publication number
JPH0541585B2
JPH0541585B2 JP58069743A JP6974383A JPH0541585B2 JP H0541585 B2 JPH0541585 B2 JP H0541585B2 JP 58069743 A JP58069743 A JP 58069743A JP 6974383 A JP6974383 A JP 6974383A JP H0541585 B2 JPH0541585 B2 JP H0541585B2
Authority
JP
Japan
Prior art keywords
weight
molding
denture base
mixture
hemihydrate gypsum
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
Application number
JP58069743A
Other languages
Japanese (ja)
Other versions
JPS59195561A (en
Inventor
Tatsuo Goto
Teruo Tsumato
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP58069743A priority Critical patent/JPS59195561A/en
Publication of JPS59195561A publication Critical patent/JPS59195561A/en
Publication of JPH0541585B2 publication Critical patent/JPH0541585B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は熱可塑性樹脂を用い、圧縮成形法によ
り義歯床を成形する場合に使用するための石こう
型材料に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a plaster mold material for use in molding a denture base by compression molding using a thermoplastic resin.

従来、圧縮成形法による義歯床の製造法として
は、アクリル系のモノマーとポリマーの混合物を
用いて成形後、室温または加熱重合する方法が知
られているが、熱可塑性樹脂を用いた圧縮成形法
については知られていない。本発明者は該圧縮成
形法を開発し、さきに特許出願を行つた(特願昭
56−99892号)。
Conventionally, methods for manufacturing denture bases using compression molding methods include molding using a mixture of acrylic monomers and polymers, followed by polymerization at room temperature or under heating; however, compression molding methods using thermoplastic resins is not known about. The present inventor developed the compression molding method and filed a patent application earlier.
56-99892).

その方法は、下部フラスコ内の石こう型の上に
義歯床用熱可塑性樹脂をのせ、恒温加熱槽に入
れ、熱風で軟化させた後、上部フラスコ内の石こ
う型を合わせ圧縮成形を行ない、義歯床を得る方
法である。
The method is to place the thermoplastic resin for the denture base on the plaster mold in the lower flask, place it in a constant temperature heating tank, soften it with hot air, then fit it with the plaster mold in the upper flask and perform compression molding. This is the way to obtain.

従来のアクリル系のモノマーとポリマーの混合
物を用いる圧縮成形法では、餅状の混合レジンを
準備された型に填入し、フラスコの上下盒を閉
じ、フラスコ・プレスに挾んで、加圧成形後、室
温もしくは加熱により重合させるが、アクリルモ
ノマーの沸点が100℃であるため、通常100℃以下
で重合処置が行なわれている。したがつて、義歯
床成形用型材の耐熱性は100℃で十分であり、ア
ルフア形半水石こう、ベータ型半水石こう、シリ
コン系材料、寒天など比較的耐熱性の高いものが
使用されていた。
In the conventional compression molding method using a mixture of acrylic monomers and polymers, a rice cake-like mixed resin is put into a prepared mold, the top and bottom of the flask are closed, and the flask is placed in a flask press. Polymerization is carried out at room temperature or by heating, but since the boiling point of acrylic monomers is 100°C, polymerization is usually carried out at temperatures below 100°C. Therefore, the heat resistance of mold materials for denture base molding is sufficient at 100°C, and materials with relatively high heat resistance such as alpha-type hemihydrate gypsum, beta-type hemihydrate gypsum, silicone-based materials, and agar were used. .

しかしながら、前記熱可塑性樹脂を用いた圧縮
成形法では、下部フラスコ内の石こう型上で該熱
可塑性樹脂を加熱軟化させる必要から、石こう型
も200℃ないし400℃に昇温する。したがつて石こ
う型として約400℃に耐える材料が必要であるが、
前記半水石こうシリコン系材料、寒天などでは
200℃ないし400℃に加熱された場合極めて大きな
強度低下、剛性低下があり使用に耐えないことが
わかつた。
However, in the compression molding method using the thermoplastic resin, it is necessary to heat and soften the thermoplastic resin on the plaster mold in the lower flask, so the temperature of the plaster mold is also raised to 200°C to 400°C. Therefore, a material that can withstand temperatures of approximately 400°C is required for the plaster mold.
In the above-mentioned hemihydrate gypsum silicon-based materials, agar, etc.
It was found that when heated to 200℃ to 400℃, there was an extremely large decrease in strength and rigidity, making it unusable.

本発明の目的は、上記圧縮成形法において良好
な成形性、すなわち、熱可塑性樹脂を軟化させる
温度における加圧成形に耐え、かつ冷却後成形さ
れた義歯床を容易にとり出すことができる石こう
型用の材料を提供することである。
The object of the present invention is to provide a plaster mold that has good moldability in the above-mentioned compression molding method, that is, can withstand pressure molding at a temperature that softens the thermoplastic resin, and that allows the molded denture base to be easily taken out after cooling. The goal is to provide materials for

本発明者は研究の結果、アルフア型半水石こう
と二酸化ケイ素が特定の比率で含有する混合物を
使用することにより、好結果が得られることを見
い出し本発明に到達した。
As a result of research, the present inventors have discovered that good results can be obtained by using a mixture containing alpha hemihydrate gypsum and silicon dioxide in a specific ratio, and have arrived at the present invention.

すなわち、本発明はアルフア型半水石こうが50
〜80重量%、二酸化ケイ素が50〜20重量%の比率
で混合されてなる熱可塑性樹脂製義歯床成形用石
こう型材料である。
That is, in the present invention, alpha-type hemihydrate gypsum is
This is a plaster-type material for molding a denture base made of thermoplastic resin, which is made of a mixture of silicon dioxide at a ratio of ~80% by weight and silicon dioxide at a ratio of 50 to 20% by weight.

本発明に使用されるアルフア型半水石こうは石
こうの主原料である二水石こう(CaSO4
2H2O)を湿式(例えばオートクレーブ中で水蒸
気をかけて120−130℃で軽焼き)加熱することに
よつて得られ、α−CaSO4・1/2H2Oの化学式で
表示されるものである。二水石こうの乾式加熱に
よつて得られるベータ形半水石こう(β−
CaSO4・1/2H2O)と対比される。
The alpha-type hemihydrate gypsum used in the present invention is dihydrate gypsum ( CaSO4 .
It is obtained by wet heating (e.g. lightly baking at 120-130℃ in an autoclave with steam applied to it) and is expressed by the chemical formula α - CaSO 4 1/2H 2 O. be. Beta-type hemihydrate gypsum (β-
CaSO 4 1/2H 2 O).

本発明に使用される二酸化ケイ素は一般に
SiO2であらわされ、シリカ、無水ケイ酸、また
は単ケイ酸などと言われることもある。二酸化ケ
イ素の中の同質異形体として、クリストバライ
ト、石英、トリジマイト、溶融無水ケイ酸などが
ある。
The silicon dioxide used in the present invention is generally
It is expressed as SiO 2 and is sometimes called silica, silicic anhydride, or monosilicic acid. Allomorphs of silicon dioxide include cristobalite, quartz, tridymite, and fused silicic anhydride.

配合量としては、アルフア型半水石こうが40〜
90重量%、二酸化ケイ素が60〜10重量%の比率で
混合されたものが有効である。すなわち、アルフ
ア型半水石こうが90重量%を越え、二酸化ケイ素
が10重量%未満の混合物から得られた型材を使用
した場合には、熱可塑性樹脂を軟化させる温度で
石こう型の強度低下が大きく、加圧時に石こう型
の破損が生じ、良好な成形が行えない。また、ア
ルフア型半水石こうが40重量%未満、二酸化ケイ
素が60重量%を越える場合には、室温状態におい
ても機械的強度が低く使用に耐えない。
The blending amount is 40 ~ alpha type hemihydrate gypsum.
A mixture of 90% by weight and 60 to 10% by weight of silicon dioxide is effective. In other words, when using a mold material obtained from a mixture containing more than 90% by weight of alpha-type hemihydrate gypsum and less than 10% by weight of silicon dioxide, the strength of the gypsum mold will decrease significantly at temperatures that soften the thermoplastic resin. , damage to the plaster mold occurs during pressurization, making it impossible to perform good molding. Furthermore, if the alpha-type hemihydrate gypsum is less than 40% by weight and the silicon dioxide content is more than 60% by weight, the mechanical strength is low even at room temperature and cannot be used.

また、ベータ形半水石こうをアルフア型半水石
こうの代りに用いた場合も強度不足であり、良好
な義歯床成形が行えない。
Furthermore, when beta-type hemihydrate gypsum is used instead of alpha-type hemihydrate gypsum, the strength is insufficient and good denture base molding cannot be performed.

本発明のアルフア型半水石こうと二酸化ケイ素
を前記比率に混合されたものを用いた時にのみ該
圧縮成形の高温、加圧条件に耐える強度を有し、
かつ、冷却後の成形品取出し時には、石こう型は
脆くなつており、容易に石こうを破壊、除去する
ことができ、成形された義歯床を何ら傷つけるこ
となく円滑に短時間に取り出すことができる。こ
の特性はアルフア型半水石こうが50〜80重量%、
二酸化ケイ素が50〜20重量%の時、一層効果的に
発揮され、より好ましい。
Only when the alpha-type hemihydrate gypsum and silicon dioxide of the present invention are mixed in the above ratio, it has the strength to withstand the high temperature and pressure conditions of compression molding,
Moreover, when the molded product is taken out after cooling, the plaster mold is brittle, and the plaster can be easily destroyed and removed, and the molded denture base can be taken out smoothly and in a short time without any damage. This property is due to alpha-type hemihydrate gypsum of 50 to 80% by weight,
When the silicon dioxide content is 50 to 20% by weight, it is more effective and is more preferable.

さらに、該熱可塑性樹脂の加熱時、石こうは脱
水現象により収縮するが、二酸化ケイ素は膨張す
るため、本発明による混合物を使用した型の場合
には、石こうの収縮と二酸化ケイ素の膨張が相殺
されて型窩の寸法に大きな変化がなく、原形に忠
実な寸法の義歯床が得られるという利点も有する
ことがわかつた。本発明に使用される二酸化ケイ
素の内、特にクリストバライトは石英、トリジマ
イト、溶融無水ケイ酸に比べ、200℃以上で膨張
が大きいが、温度依存性は小さいという現象を示
すため、200℃以上の成形温度条件の変動による
型窩寸法の変化が小さく、より原形に忠実な義歯
床が得られるため、好ましい。
Furthermore, when heating the thermoplastic resin, gypsum contracts due to dehydration phenomena, while silicon dioxide expands, so that in the case of molds using the mixture according to the invention, the contraction of gypsum and the expansion of silicon dioxide are offset. It has been found that this method has the advantage that there is no major change in the dimensions of the mold cavity, and that a denture base with dimensions that are faithful to the original shape can be obtained. Among the silicon dioxides used in the present invention, cristobalite in particular exhibits a phenomenon in which it expands more at temperatures above 200°C than quartz, tridymite, and fused silicic anhydride, but its temperature dependence is small. This is preferable because the change in mold cavity dimensions due to fluctuations in temperature conditions is small and a denture base that is more faithful to the original shape can be obtained.

本発明にかかる混合物を得るための配合方法と
しては、特に限定はなく、通常実施されている振
盪による方法、機械的混合法などが使用可能であ
る。
The blending method for obtaining the mixture according to the present invention is not particularly limited, and commonly used methods such as shaking and mechanical mixing can be used.

本発明の混合物には、混合物本来の強度、熱的
特性に悪影響を与えない範囲で、必要に応じて、
硬化時間を調節するための促進剤や遅延剤、着色
剤等を少量添加することができる。
The mixture of the present invention may contain, if necessary, as long as it does not adversely affect the inherent strength and thermal properties of the mixture.
Small amounts of accelerators, retarders, colorants, etc. can be added to adjust the curing time.

本発明において使用される熱可塑性樹脂として
は、該成形方法で熱的に劣化を起さず、かつ適度
な粘度を有し、良好な賦型性をもち、歯肉に近似
した色に着色が可能で、適度な剛性と耐湿性を有
し、かつ使用時にストレスクラツクを起さない強
靭性を備えた樹脂であることが要求される。した
がつて、ポリスチレン、ポリメチルメタクリレー
ト、ポリメチルペンテン−1、透明ナイロン、ポ
リエチレンテレフタレート、ポリカーボネート、
ポリアリレート、ポリエステルカーボネート、透
明ABS樹脂、ポリサルホン系樹脂などが使用さ
れるが、特にポリサルホン、ポリエーテルサルホ
ンなどポリサルホン系の樹脂が耐湿性、剛性、耐
ストレスクラツキング性などにすぐれており、好
ましい。本発明で好ましい態様として使用される
ポリサルホン系樹脂はアリーレン単位がエーテル
およびスルホン結合と共に無秩序にまたは秩序正
しく位置するポリアリーレンポリエーテルポリサ
ルホンとして定義される。たとえば の構造を有するUCC製ポリサルホンUdel や の構造を有するICI製のポリエーテルサルホン
Vichrex が挙げられる。
The thermoplastic resin used in the present invention does not undergo thermal deterioration through the molding method, has an appropriate viscosity, has good moldability, and can be colored in a color similar to that of the gums. Therefore, it is required that the resin has appropriate rigidity and moisture resistance, as well as toughness that does not cause stress cracks during use. Therefore, polystyrene, polymethyl methacrylate, polymethylpentene-1, transparent nylon, polyethylene terephthalate, polycarbonate,
Polyarylate, polyester carbonate, transparent ABS resin, polysulfone resin, etc. are used, but polysulfone resins such as polysulfone and polyethersulfone have excellent moisture resistance, rigidity, stress cracking resistance, etc. preferable. The polysulfone resin used as a preferred embodiment in the present invention is defined as a polyarylene polyether polysulfone in which arylene units are located in a disordered or ordered manner with ether and sulfone bonds. for example UCC polysulfone Udel with the structure Polyethersulfone manufactured by ICI with the structure of
One example is Vichrex.

以下実施例により本発明を具体的に説明するが
これらは好適な態様の例示であつて、実施例の組
成に限定されるものではない。
The present invention will be specifically explained below with reference to Examples, but these are merely illustrative of preferred embodiments and are not limited to the compositions of the Examples.

実施例 1 アルフア型半水石こう70重量%、クリストバラ
イト30重量%を機械的に十分混合した後、該混合
物を0.25倍(重量倍率)の水と混和し、ワツクス
製の義歯床模型を位置させたフラスコ内に流し込
み硬化させる。
Example 1 After 70% by weight of alpha-type hemihydrate gypsum and 30% by weight of cristobalite were thoroughly mixed mechanically, the mixture was mixed with 0.25 times (weight ratio) water, and a wax denture base model was placed. Pour into a flask and let harden.

石こう/クリストバライト混合物が硬化後、該
ワツクスを通法により加熱軟化させ流出させる。
該ワツクスが除去された下蓋部に該ワツクスに相
当する容積を有するポリエーテルサルホン(ICI
製Victrex 200P)の歯肉様に着色されたU字型
成形品を位置させ、360℃の熱風を吹きつけ、加
熱軟化させる。軟化した成形品上に、該ワツクス
が、除去された人工歯を内蔵する上蓋部を圧着す
ることによつて上蓋部と下蓋部の間の、該ワツク
スが除去された空洞部にポリエーテルサルホンを
填入せしめる。冷却後フラスコの金属製枠を除去
し、人工歯と一体化したポリエーテルサルホン製
義歯床をとり出した。
After the gypsum/cristobalite mixture has hardened, the wax is softened by heating and drained.
Polyethersulfone (ICI) having a volume corresponding to the wax is placed on the lower lid from which the wax has been removed.
Place a U-shaped molded product made of Victrex 200P (manufactured by Victrex 200P) colored to resemble gums, and blow hot air at 360°C to heat and soften. By pressing the upper lid part containing the removed artificial tooth onto the softened molded product, a polyether resin is applied to the cavity between the upper lid part and the lower lid part from which the wax has been removed. Insert the phone. After cooling, the metal frame of the flask was removed, and the polyethersulfone denture base integrated with the artificial tooth was taken out.

とり出されたポリエーテルサルホン製義歯床は
該ワツクス模型の形が忠実に再現されており、表
面光沢も良好で十分実用性のあるものであつた。
これは、360℃熱風加熱および加圧圧着時におい
ても石こう/クリストバライト混合型はクラツ
ク、破損なく該成形条件に十分耐え得たことを示
している。また成形後の石こう混合物の除去は水
中で容易に成形品からとり除くことができた。さ
らに石こうの収縮とクリストバライトの膨張によ
り、該ワツクス模型が除去された空洞部の寸法変
化が加熱時も極めて少ないため、義歯床成形品寸
法は該ワツクス模型に極めて近似した寸法に仕上
つていた。
The extracted polyethersulfone denture base faithfully reproduced the shape of the wax model, had good surface gloss, and was sufficiently practical.
This indicates that the gypsum/cristobalite mixed type was able to sufficiently withstand the molding conditions without cracking or breakage even during 360°C hot air heating and pressure bonding. Furthermore, the gypsum mixture after molding could be easily removed from the molded product in water. Furthermore, due to the contraction of the gypsum and the expansion of the cristobalite, the dimensional change in the cavity where the wax model was removed was extremely small even during heating, so the denture base molded product was finished in dimensions that were extremely similar to the wax model.

実施例 2 アルフア型半水石こう60重量%、トリジマイト
40重量%混合品を義歯床成形用石こう型材料とし
て使用する以外は、すべて実施例1と同様の条件
で成形し、成形品を石こう型からはずした所、実
施例1と同様ワツクス模型と近似した寸法を有す
る良好な義歯床が得られた。
Example 2 Alpha-type hemihydrate gypsum 60% by weight, tridymite
The molding was performed under the same conditions as in Example 1, except that the 40% by weight mixture was used as the plaster mold material for denture base molding, and when the molded product was removed from the plaster mold, it resembled the wax model as in Example 1. A good denture base with the following dimensions was obtained.

比較例 1 アルフア型半水石こう95重量%、クリストバラ
イト5重量%混合品を義歯床成形用石こう型材料
として使用する以外は、すべて実施例1と同様の
条件で成形した所、加圧圧着時に石こう型が破損
し、ワツクス模型と比べ、成形品肉厚、形状が異
なり、充填性も不十分であり、良好な成形が行え
なかつた。
Comparative Example 1 Molding was carried out under the same conditions as in Example 1 except that a mixture of 95% by weight of alpha-type hemihydrate gypsum and 5% by weight of cristobalite was used as the plaster mold material for denture base molding. The mold was damaged, and compared to the wax model, the thickness and shape of the molded product were different, and the filling properties were insufficient, making it impossible to perform good molding.

比較例 2 アルフア型半水石こう30重量%、クリストバラ
イト70重量%混合物を義歯床成形用石こう型材料
として使用する以外はすべて実施例1と同様の条
件で成形した所、比較例1と同様、加圧時に石こ
う型が破損し、良好な成形が行えなかつた。
Comparative Example 2 Molding was carried out under the same conditions as in Example 1 except that a mixture of 30% by weight of alpha-type hemihydrate gypsum and 70% by weight of cristobalite was used as the plaster mold material for denture base molding. The plaster mold was damaged during pressing, and good molding could not be achieved.

比較例 3 ベータ型形半水石こう70重量%、クリストバラ
イト30重量%混合品を義歯床成形用石こう型材料
として使用する以外は、すべて実施例1と同様の
条件で成形した所、加圧圧着時に石こう型が破損
し、比較例1と同様良好な成形が行えなかつた。
Comparative Example 3 Molding was performed under the same conditions as in Example 1, except that a mixture of 70% by weight beta-type hemihydrate gypsum and 30% by weight cristobalite was used as the plaster mold material for denture base molding. The plaster mold was damaged, and as in Comparative Example 1, good molding could not be performed.

Claims (1)

【特許請求の範囲】[Claims] 1 アルフア型半水石こうが50〜80重量%、二酸
化ケイ素が50〜20重量%の比率で混合されてなる
熱可塑性樹脂製義歯床圧縮成形用石こう型材料。
1. A thermoplastic resin denture base compression molding plaster molding material made of a mixture of 50 to 80% by weight of alpha-type hemihydrate gypsum and 50 to 20% by weight of silicon dioxide.
JP58069743A 1983-04-19 1983-04-19 False tooth bed forming gypsum molding material Granted JPS59195561A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58069743A JPS59195561A (en) 1983-04-19 1983-04-19 False tooth bed forming gypsum molding material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58069743A JPS59195561A (en) 1983-04-19 1983-04-19 False tooth bed forming gypsum molding material

Publications (2)

Publication Number Publication Date
JPS59195561A JPS59195561A (en) 1984-11-06
JPH0541585B2 true JPH0541585B2 (en) 1993-06-23

Family

ID=13411584

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58069743A Granted JPS59195561A (en) 1983-04-19 1983-04-19 False tooth bed forming gypsum molding material

Country Status (1)

Country Link
JP (1) JPS59195561A (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4712220Y1 (en) * 1969-08-08 1972-05-06

Also Published As

Publication number Publication date
JPS59195561A (en) 1984-11-06

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