JPS6150906A - Dental adhesive - Google Patents
Dental adhesiveInfo
- Publication number
- JPS6150906A JPS6150906A JP59173484A JP17348484A JPS6150906A JP S6150906 A JPS6150906 A JP S6150906A JP 59173484 A JP59173484 A JP 59173484A JP 17348484 A JP17348484 A JP 17348484A JP S6150906 A JPS6150906 A JP S6150906A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- dental
- acrylic resin
- methylene chloride
- adhesive
- 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
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- Dental Preparations (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野 □
本発明は、歯科用ポリサルホン系樹脂と歯科用アクリル
系樹脂とを接着させる接着剤に関する。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application □ The present invention relates to an adhesive for bonding a dental polysulfone resin and a dental acrylic resin.
従来の技術
従来の樹脂製歯科補綴物は、長年の間アクリル系樹脂を
用い、ポリマーとモノマーの加熱重合による加圧成形法
により得ていた。これは補修材料として同一の7クリル
ポリマー粉末と7クリルモノマー液を用いろため補修が
簡便である利点があつrこ。BACKGROUND OF THE INVENTION Conventional dental prostheses made of resin have been produced using acrylic resins for many years by pressure molding by heating and polymerizing polymers and monomers. This has the advantage that repairs are easy because the same 7-acrylic polymer powder and 7-acrylic monomer liquid are used as the repair materials.
しかし、このようなアクリル系樹脂の加熱重合により得
られTζ歯科補綴物は脆く、薄い部分は咬合力により破
折することが多い強度的な欠点とともに、加熱重合反応
が不十分な場合が多い゛ため、残留モノマーが溶出して
アレルギー症状を起すといつ1こ衛生上の欠点をも有す
るものであり1こ。However, Tζ dental prostheses obtained by heating polymerization of such acrylic resins are brittle, and the thin portions often break due to occlusal force, which is a strength disadvantage, and the heating polymerization reaction is often insufficient. Therefore, if the residual monomer is eluted and causes allergic symptoms, it also has a hygienic drawback.
ま1こ、アクリル樹脂製人工歯は歯ブラシにより摩耗し
やすいなどの欠点もある。However, artificial teeth made of acrylic resin also have the disadvantage of being easily abraded by toothbrushes.
このようなアクリル系樹脂製歯科補綴物の欠点を除去す
るものとしてポリサルホン系樹脂による歯科補綴物が提
案され、実用化され ゛るようになりて来た、
このポリサルホン系樹脂はエンジニアリングプラスチッ
クの一独で機械的強度が高く、耐衝撃性にすぐれている
が、従来一般的に使用□されているアクリル樹脂製人工
歯との接着性がわるく、特別の維持装置や通常の接着剤
を使用してもなお、接着性が不十分であり、実用上、例
えば比較的硬い食物を咬んだ際などに人工歯がはずれや
すいなどの問題がある。Dental prosthetics made of polysulfone resin have been proposed to eliminate these drawbacks of dental prosthetics made of acrylic resin, and have come into practical use.This polysulfone resin is a unique engineering plastic. Although it has high mechanical strength and excellent impact resistance, it has poor adhesion with the commonly used acrylic resin artificial teeth, so it is difficult to use special retaining devices or ordinary adhesives. However, the adhesion is insufficient, and there are practical problems such as the fact that the artificial teeth tend to come off when biting into relatively hard food, for example.
まfこ、アクリル樹脂製義歯床の口がい部の肉厚調整等
に使用されるアクリル樹脂系の硬質裏装剤や暫間裏装剤
などのいわゆるリベース剤8該ボッサルホン系樹脂製歯
科補綴物に適用しても十分な接着性が得られず、実用に
供し得ないのが実情であつtこ。So-called rebase agents such as acrylic resin hard lining agents and temporary lining agents used for adjusting the wall thickness of the mouth part of acrylic resin denture bases 8. Bossalphone resin dental prostheses The actual situation is that even if it is applied to a material, sufficient adhesion cannot be obtained and it cannot be put to practical use.
発明が解決しようとする問題点
本発明は歯科用ポリサルホン系樹脂と歯科用アクリル系
樹脂とを強固に接着させることができる歯科用接着剤を
提供することを目的とするものである。すなわち、ポリ
サルホン系樹脂製義歯床とアクリル樹脂製人工歯、ポリ
サルホン系樹脂製義歯床とアクリル樹脂系リベース剤、
アクリル樹脂89歯床とポリサルホン系樹脂製人工歯な
どを強固に接着し、その実用性の範囲を飛躍的に拡大す
る接着剤を提供するものである。Problems to be Solved by the Invention The object of the present invention is to provide a dental adhesive capable of firmly bonding a dental polysulfone resin and a dental acrylic resin. That is, a polysulfone resin denture base and an acrylic resin artificial tooth, a polysulfone resin denture base and an acrylic resin rebase agent,
The present invention provides an adhesive that firmly adheres an acrylic resin 89 tooth base to an artificial tooth made of polysulfone resin, and dramatically expands the range of its practicality.
問題点を解決するための手段
本発明の特徴とするところは、歯科用ポリサルホン系樹
脂と歯科用アクリル系樹脂とを接着させるに際して用い
ろ接着剤が、塩化メチレンとポリカーボネート樹脂から
なり、塩化メチレン100重量部に対して、ポリカーボ
ネート樹脂が0.8〜20Mflk部含有してなる歯科
用接着剤である。Means for Solving the Problems The present invention is characterized in that the adhesive used to bond the dental polysulfone resin and the dental acrylic resin is made of methylene chloride and a polycarbonate resin; This dental adhesive contains 0.8 to 20 Mflk parts of polycarbonate resin based on parts by weight.
本発明において使用されるポリカーボネート樹脂は4.
4−ジオキシジアリルフルカン系ポリカーボネートであ
り、たとえばビス(4−ヒドロキシフェニル)メタン、
ビス(4−ヒドロキシフェニル)エタン、2.2−ヒス
(4−ヒドロキシフェニル〕プロパン、ビス〔4−ヒド
ロキシ−8,5−ジクロロフェニル〕メタン、2.2−
ビス(4−ヒドロキシ−8,5−ジメチルフェニル〕プ
ロパン、ビス〔4−ヒドロキシフェニル〕フェニルメタ
ン等の4.4−ジオキシジフェニルアルカンとホスゲン
あるいはジフェニルカーボネートより得られるものであ
る。このようなポリカーボネートはすでに公知の溶融重
合、液液重合、界面重合など各種方法により製造される
。The polycarbonate resin used in the present invention is 4.
4-dioxydiallylphurcan-based polycarbonate, such as bis(4-hydroxyphenyl)methane,
Bis(4-hydroxyphenyl)ethane, 2.2-his(4-hydroxyphenyl)propane, bis[4-hydroxy-8,5-dichlorophenyl]methane, 2.2-
It is obtained from 4,4-dioxydiphenylalkanes such as bis(4-hydroxy-8,5-dimethylphenyl)propane and bis[4-hydroxyphenyl]phenylmethane and phosgene or diphenyl carbonate. Such polycarbonates can be produced by various methods already known, such as melt polymerization, liquid-liquid polymerization, and interfacial polymerization.
本発明において使用される塩化メチレンは化学式CH2
C/ 2で表わされ、二塩化メチレン、ジクロロメタン
ともいわれる。融点−97℃、沸点40℃の無色の液体
である。The methylene chloride used in the present invention has the chemical formula CH2
It is represented by C/2 and is also called methylene dichloride or dichloromethane. It is a colorless liquid with a melting point of -97°C and a boiling point of 40°C.
マTこ、本発明において、塩化メチレン中のポリカーボ
ネート樹脂の含有量は、塩化メチレン100重量部に対
してポリカーボネート樹脂が0.8〜20重量部が適当
である。In the present invention, the content of polycarbonate resin in methylene chloride is suitably 0.8 to 20 parts by weight per 100 parts by weight of methylene chloride.
塩化メチレン100重役部に対して、ポリカーボネート
樹脂が0.8311iffi部未満であれば歯科用ポリ
サルホン系樹脂と歯科用アクリル系樹脂との接着が十分
でなく、ポリカーボネート樹脂の含有量が20:Tf量
部を越えると溶液の粘度が高すぎ、均一な塗布が困難で
、好ましくない。さらに、ポリカーボネート樹脂−の含
有量が0.6〜15重量部の時、接着時の作業性、乾燥
効率、接着強度等においてバランスのとれた特性を百し
、好ヱしい。If the polycarbonate resin is less than 0.8311 iffi parts per 100 parts of methylene chloride, the adhesion between the dental polysulfone resin and the dental acrylic resin will not be sufficient, and the content of the polycarbonate resin will be 20 parts by Tf. Exceeding this is not preferable because the viscosity of the solution is too high and uniform application is difficult. Furthermore, when the content of the polycarbonate resin is 0.6 to 15 parts by weight, it is preferable because it provides well-balanced properties in terms of workability during adhesion, drying efficiency, adhesion strength, etc.
本発明に使用される該ポリカーボネート樹脂/塩化メチ
レン溶液にポリメチルメタクリレート(以下F M M
人と略す〕、メチルメタクリレートモノマー〔以下MM
Aと略T〕を目的に応じて適当量配合することが可能で
ある。Polymethyl methacrylate (hereinafter referred to as F M M
(abbreviated as “person”), methyl methacrylate monomer (hereinafter referred to as “MM”)
A and T] can be blended in appropriate amounts depending on the purpose.
例えばポリサル示ン製義歯床とアクリル系樹脂製リベー
ス剤との接着に、該ポリカーボネート樹脂/塩化メチレ
ン溶液を用いる際、さらに該溶液にPMMAを適当量配
合するとより強固な接着が達成され、またMMムを配合
すると、該接着部分およびその周縁に光沢性を与え、よ
り艮好な外観か得られる効果がある。For example, when using the polycarbonate resin/methylene chloride solution to bond a polysulfur denture base and an acrylic resin rebase agent, if an appropriate amount of PMMA is added to the solution, stronger adhesion can be achieved. When blended with rubber, the bonded area and its periphery are given gloss and a more attractive appearance can be obtained.
なお、本発明に使用されろ該ポリカーボネート樹脂/塩
化メチレン溶液に対して、本発明の目的を損わない範囲
で、染料、顔料などの着色剤、紫外線吸収剤、安定剤な
ど通常の添加剤を181以上添加する仁とができる。The polycarbonate resin/methylene chloride solution used in the present invention may contain conventional additives such as coloring agents such as dyes and pigments, ultraviolet absorbers, and stabilizers, to the extent that the purpose of the present invention is not impaired. 181 or more kernels can be added.
また、本発明でいう歯科用ポリサルホン系樹脂とは、7
リ一レン単位がエーテルおよびスルホン結合とともに無
秩序にまたは秩序正しく位置するボリアリーレシボリエ
ーテルボリサルホシをいい、たとえば
CH2
の構造を有するυCC製ポリサルホンUdel■I C
I 製oyホリエ−f ル+ /L/* :/ Vic
trex■などを含み、歯科補綴物として使用可能な衛
生性にすぐれた樹脂およびフンパウンドをいう。In addition, the dental polysulfone resin referred to in the present invention is 7
It refers to polyarylethyl ether borisulfo in which lylene units are located randomly or orderly together with ether and sulfone bonds, for example, υCC polysulfone Udel IC with the CH2 structure.
I made oy holier-f le+ /L/*:/Vic
This refers to resins and powders with excellent hygiene that can be used as dental prostheses, including trex■, etc.
本発明でいう歯科用アクリル系樹脂とはMMムの単独重
合体(PMMム)、ブチルメタクリレートなど他のメタ
クリレートとの共重合体など、歯科補綴物として使用さ
れるアクリル系樹脂をいう。The dental acrylic resin used in the present invention refers to an acrylic resin used as a dental prosthesis, such as a homopolymer of MM (PMM) or a copolymer with other methacrylate such as butyl methacrylate.
本発明の接着剤で、歯科用ポリサルホン系樹脂と歯科用
アクリル系樹脂を接着する方法は特に限定されない。例
えば、一方もしくは双方の被着体面に本発明の接着剤を
塗布し、数秒〜数分の風乾の後、双方の被着体面を合わ
せ、軽く加圧した後、さらに80℃前後で10−100
分程度の熱処理を行なう方法や、ポリサル本ン樹脂l!
!歯科補綴物の上に、本発明の接着剤を塗布し、風乾後
、市販のアクリル樹脂系のりベース剤を塗布する方法な
どいずれの方法も過用が可能である。The method of bonding dental polysulfone resin and dental acrylic resin with the adhesive of the present invention is not particularly limited. For example, the adhesive of the present invention is applied to one or both adherend surfaces, air-dried for a few seconds to several minutes, then both adherend surfaces are brought together, lightly pressed, and then heated to 10-100°C at around 80°C.
How to perform heat treatment for about minutes, polysal resin l!
! It is possible to overuse any method such as applying the adhesive of the present invention on the dental prosthesis, air-drying it, and then applying a commercially available acrylic resin adhesive base.
作 用
木兄肌におけろポリカーボネート樹脂の塩化メチレジ溶
液を、ポリサルホン系樹脂、アクリル系樹脂の被着界面
に介在させ、風乾もしくは、適度の熱処理により溶剤を
除去すると驚くべきことに極めて強固な接着強度が得ら
れる。How it works When a solution of methylene chloride of polycarbonate resin is interposed at the adhesion interface of polysulfone resin and acrylic resin, and the solvent is removed by air drying or moderate heat treatment, surprisingly strong adhesion is achieved. Provides strength.
これはポリカーボネート樹脂が、ポリサルホン系樹脂、
アクリル系樹脂と本質的な分子構造の違いを可しながら
も、ポリサルホン系樹脂、アクリル系樹脂の双方に比較
的高い親和性をもりており、接着界面では分子レベルに
近い良好な分散状態が得られていることが推定される。This is polycarbonate resin, polysulfone resin,
Although it has an essential molecular structure difference from acrylic resins, it has a relatively high affinity for both polysulfone resins and acrylic resins, and a good dispersion state close to the molecular level can be achieved at the adhesive interface. It is presumed that the
また、塩化メチレンは低沸点で乾燥が早く、歯科用ポリ
サルホン系樹脂に塗布してもクラックを発生させない。Furthermore, methylene chloride has a low boiling point and dries quickly, so it does not cause cracks even when applied to dental polysulfone resin.
tlこ、ポリカーボネート樹脂の良溶剤であり、均一な
溶醍の調製が可能であり、さらに歯科用アクリル系樹脂
との親和性も良好である。さらに、塩素溶剤の中では安
全衛生性の面でも良好である。It is a good solvent for polycarbonate resins, allows for the preparation of uniform melts, and also has good affinity with dental acrylic resins. Furthermore, it has good safety and hygiene characteristics among chlorinated solvents.
以下、実施例により本発明を具体的に説明するが、これ
は好適な態様の例示であって、本発明は実施例の範囲に
限定されるものではない。Hereinafter, the present invention will be specifically explained with reference to Examples, but these are illustrative of preferred embodiments, and the present invention is not limited to the scope of the Examples.
実施例1
日本工業規格JI8 T−6511に記載された人工
歯破折試験法に従い、第1図のとおりアクリル樹脂製人
工歯(ジ−シーアクリリックレジン前#1)lを、切端
部1′と歯頚部1′を結ぶ線がパラフィンワックス原盤
と45゜の角度となるようにパラフィンワックス原型に
植付け、フラスコ内に石こう埋没後、流ろうし、石こう
型を形成させた。Example 1 According to the artificial tooth fracture test method described in Japanese Industrial Standards JI8 T-6511, an acrylic resin artificial tooth (GC acrylic resin front #1) l was placed between the incisal end 1' and It was planted on a paraffin wax model so that the line connecting the tooth neck 1' was at an angle of 45° with the paraffin wax master, and after embedding plaster in a flask, it was poured with wax to form a plaster mold.
この石こう臘を射出成形機に取りつけ、シリンダ一温度
850℃、射出圧力1500 1に@/cs
2、射出m[200M/秒(成形機:住友−ネスタール
P40725)の条件で、歯肉様に着色されたポリサル
ホン樹脂(UCC!製Udel■P−1700)の溶融
樹脂をフラスコ内へ射出注入した。Attach this gypsum to an injection molding machine, set the cylinder temperature to 850℃ and the injection pressure to 1500℃ @/cs
2. Under the conditions of injection m [200 M/sec (molding machine: Sumitomo Nestal P40725), molten resin of polysulfone resin colored like gums (Udel P-1700 manufactured by UCC!) was injected into the flask.
冷却後、フラスコを分割し、人工歯破折試駿用成形品を
とり出した。人工歯を手で強くひっばると人工歯は成形
品からはずれた。人工歯のはずれた臣洞部へ塩化メチレ
ン100M爪部、ポリカーボネート樹脂(三菱ガス化学
製ニーピロン■82000)10ffi量部からなる溶
液を譲塗りし、数秒の風乾の後、先にはずしfこアクリ
ル樹脂製人工歯をそう人し、軽く加圧した。その後80
℃の熱風乾燥炉で40分の熱処理を行つtご。After cooling, the flask was divided into parts, and molded articles for artificial tooth fracture testing were taken out. When the artificial tooth was pulled strongly by hand, it came off from the molded product. Apply a solution consisting of 100M methylene chloride nail part and 10 parts polycarbonate resin (Mitsubishi Gas Chemical Kneepilon 82000) to the hollow part of the artificial tooth, and after air-drying for a few seconds, remove the acrylic resin first. The prepared artificial tooth was then placed and lightly pressurized. After that 80
Heat treatment for 40 minutes in a hot air drying oven at ℃.
得られfコ成形品を第1図のごとく樹脂床部2を保持具
8で固定し、他方の人工歯切端部1を所定金具4を介し
て、負荷速度L2Kffン分で破折試験を行った。The resin bed part 2 of the obtained fco molded product was fixed with a holder 8 as shown in FIG. Ta.
破折強度は21Kqfであり英用土問題のない十分に高
い値を示し1こ。The fracture strength was 21 Kqf, a sufficiently high value that would not cause problems with English soil.
比較例1
実施例1と同様に、ポリサルホン樹脂をフラスコ内へ射
出注入し、冷却後フラスコを分割し、人工肉破折試験用
成形品をとり出し、何らの処理をすることなく、実鬼例
1と同様の破折試験を行つTこ。Comparative Example 1 In the same manner as in Example 1, polysulfone resin was injected into a flask, and after cooling, the flask was divided, and the molded article for the artificial meat fracture test was taken out, and a real demon example was prepared without any treatment. Perform the same fracture test as in 1.
破折強度はrKfrシかなく実用と問題となる低い値し
か示さなかつ1こ。The fracture strength was only rKfr, and only showed a low value that would pose a problem in practical use.
実抱例2
アクリル樹脂製人工歯(商品名 ジ−シー7クリリツク
レジン前歯および臼歯)が植えられ1こ義歯床ワックス
模型の埋没されtこフラスコを加熱し、ワックスを軟化
流ろうし、石こう型を形成させた。その後で、ポリニー
t #f、1zxh ン(I OI製 Victrex
■4100G)の歯肉様1こ着色されfコU字型成形品
(歯槽堤に相描する大きさを有するU字型〕を下部フラ
スコ内の石こう型上に位置させ、350℃の熱風を吹き
つけることにまり、該成形品を軟化させ7′こ。十分軟
化しγこところで上下フラスコを合わせて圧縮成形を旨
ない、その後自然冷却させた。Practical example 2 Acrylic resin artificial teeth (trade name: GC 7 Krylic Resin anterior teeth and molars) were implanted and a denture base wax model was embedded in the flask.The flask was heated to soften the wax and form a plaster mold. I let it happen. After that, Polynee t#f, 1zxh (Victrex manufactured by IOI)
■ A colored gingiva-like molded product of 4100G (U-shaped with a size that parallels the alveolar ridge) was placed on the plaster mold in the lower flask and blown with hot air at 350°C. The molded product was softened for 7'. At this point, the upper and lower flasks were put together to complete compression molding, and then allowed to cool naturally.
冷却後、上下フラスコを分割し、義歯床をとり出し1こ
。After cooling, separate the upper and lower flasks and remove the denture base.
人工歯を手で強くひっばると人工歯は義歯床からはずれ
fこ。人工歯のはずれrこ空洞部へ塩化メチレン100
重量部、ポリカーボネート樹脂15重量部からなる溶液
を薮塗りし、数秒の風乾の後、先にはずしfこ7クリル
衝脂製入工歯をそう人し、軽く加圧した。その後、80
℃の熱風乾燥炉で60分の熱処理を行つ1こっ人工歯は
強く押しても容易にはずれず、人工歯が強固に植えられ
た義歯床が得られた。If you pull the artificial tooth strongly with your hands, it will come off the denture base. Apply methylene chloride 100 to the cavity of the artificial tooth.
A solution consisting of 15 parts by weight of polycarbonate resin and 15 parts by weight of polycarbonate resin was coated on the tooth, and after air-drying for a few seconds, a 7-piece acrylic resin artificial tooth was removed and placed under light pressure. After that, 80
The artificial teeth that were heat-treated for 60 minutes in a hot air drying oven at ℃ did not come off easily even when pressed hard, and a denture base in which the artificial teeth were firmly planted was obtained.
次に、上記義歯床の口がい部に塩化メチレンtooff
iff1部、ポリカーボネート樹脂(三菱ガス化学製ニ
ーピロン■520Qcz1重量部からなる溶液を筆で塗
布し、数秒間の風乾をしrこ後、さらに、塩化メチレン
100重量部、ポリカーボネート樹脂2重量部、ポリメ
チルメタクリレート樹脂(住友化学工業製スミペックス
■MEi)1重量部からなる溶液を疵で塗布し、数秒間
風乾し1こ。Next, methylene chloride tooff was applied to the mouth part of the denture base.
A solution consisting of 1 part by weight of IFIF, 1 part by weight of polycarbonate resin (Mitsubishi Gas Chemical's Kneepilon 520Qcz) was applied with a brush, and after air-drying for a few seconds, a solution consisting of 1 part by weight of methylene chloride, 2 parts by weight of polycarbonate resin, and polymethyl was applied. A solution consisting of 1 part by weight of methacrylate resin (SumiPex MEi manufactured by Sumitomo Chemical Industries) was applied to the scratches and air-dried for a few seconds.
該溶液か塗布されfコ上に、硬質裏装剤(コー社製クー
ルライナー■)を常法に従って使用した。A hard backing material (Cool Liner ■, manufactured by Koh Co., Ltd.) was used in a conventional manner on the coated surface coated with the solution.
即ち、パラターとリキッドを昆合し、義歯床上で均等に
押し伸ばした後、硬化させfコ。That is, the paratha and the liquid are combined, pressed and stretched evenly on the denture base, and then hardened.
m 製剤1;j強固にポリエーテルサルホン製義歯床に
接着し、十分実用lζ耐えるものであった。m Formulation 1; j It adhered firmly to the polyethersulfone denture base and was sufficiently durable for practical use.
比較例2
塩化メチレンとポリカーボネート樹脂および塩化メチレ
ン、ポリカーボネート樹脂とポリメチルメタクリレート
樹脂からなる溶液をを適用しfこ。Comparative Example 2 A solution consisting of methylene chloride, polycarbonate resin, and methylene chloride, polycarbonate resin, and polymethyl methacrylate resin was applied.
裏装剤は義歯床から簡単にはずれ使用に耐えないもので
あつ1こ。The lining material is easily removed from the denture base and cannot be used.
発明の効果
以上に述べ1こ様に、本発明は、塩化メチレンとポリカ
ーボネート樹脂からなる溶液を接着剤として用いろこと
により、歯科用ポリサルホン樹脂と歯科用アクリル系樹
脂を強固に接着することが可能となり、ポリサルホン系
樹脂とアクリル系樹脂を組みあわせた歯科用補綴物の実
用範囲が飛躍的に拡大する効果が得られ1こlノ〕であ
る。Effects of the Invention As described above, the present invention makes it possible to firmly bond dental polysulfone resin and dental acrylic resin by using a solution consisting of methylene chloride and polycarbonate resin as an adhesive. This has the effect of dramatically expanding the practical range of dental prostheses that combine polysulfone resin and acrylic resin.
at図は、人工歯破折試験の実旌態様を示す側面図であ
る。
1・・・・・・・・・人工歯
1・・・・・・・・・人工歯の切端部
1′・・・・・・・・・人工歯の歯頚部2・・・・・・
・・・樹脂床部
8・・・・・・・・・保持具
4・・・・・・・・・人工歯引張り用金具第1図The at figure is a side view showing a practical aspect of the artificial tooth fracture test. 1......Artificial tooth 1...Incisal end 1' of artificial tooth...Neck part 2 of artificial tooth...
...Resin floor part 8...Holder 4...Artificial tooth tension fitting Fig. 1
Claims (1)
を接着させるに際して用いる接着剤であつて、塩化メチ
レンとポリカーボネート樹脂からなり、塩化メチレン1
00重量部に対して、ポリカーボネート樹脂が0.3〜
20重量部含有してなることを特徴とする歯科用接着剤
。An adhesive used to bond dental polysulfone resin and dental acrylic resin, consisting of methylene chloride and polycarbonate resin.
0.3 to 0.00 parts by weight of polycarbonate resin
A dental adhesive characterized by containing 20 parts by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59173484A JPS6150906A (en) | 1984-08-21 | 1984-08-21 | Dental adhesive |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59173484A JPS6150906A (en) | 1984-08-21 | 1984-08-21 | Dental adhesive |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6150906A true JPS6150906A (en) | 1986-03-13 |
JPH0447642B2 JPH0447642B2 (en) | 1992-08-04 |
Family
ID=15961355
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59173484A Granted JPS6150906A (en) | 1984-08-21 | 1984-08-21 | Dental adhesive |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6150906A (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6293209A (en) * | 1985-10-19 | 1987-04-28 | Mitsui Toatsu Chem Inc | Denture base |
JPS632855A (en) * | 1986-06-20 | 1988-01-07 | ティーディーケイ株式会社 | Ceramic material |
JPS638258A (en) * | 1986-06-26 | 1988-01-14 | ティーディーケイ株式会社 | Ceramic material |
JPS638257A (en) * | 1986-06-25 | 1988-01-14 | ティーディーケイ株式会社 | Ceramic material |
JPH02157206A (en) * | 1988-12-08 | 1990-06-18 | Kureha Chem Ind Co Ltd | Dental adhesive |
JPH076537A (en) * | 1993-04-22 | 1995-01-10 | Tdk Corp | Slider for magnetic head device and production of this slider |
US6590745B1 (en) | 1999-01-26 | 2003-07-08 | Tdk Corporation | Magnetic head, method of manufacturing same, and magnetic disk apparatus |
US7056961B2 (en) | 2000-12-04 | 2006-06-06 | Tokuyama Corporation | Adhesive composition for denture base relining material and dental curable composition |
WO2008019978A2 (en) * | 2006-08-16 | 2008-02-21 | Ivoclar Vivadent Ag | Pasty, polymerizable dental compounds and method for producing the same |
JP2009504350A (en) * | 2005-08-18 | 2009-02-05 | デンツプライ インターナショナル インコーポレーテッド | Adhesive and method for gluing artificial plastic teeth |
-
1984
- 1984-08-21 JP JP59173484A patent/JPS6150906A/en active Granted
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6293209A (en) * | 1985-10-19 | 1987-04-28 | Mitsui Toatsu Chem Inc | Denture base |
JPS632855A (en) * | 1986-06-20 | 1988-01-07 | ティーディーケイ株式会社 | Ceramic material |
JPH062616B2 (en) * | 1986-06-20 | 1994-01-12 | ティーディーケイ株式会社 | Ceramic material for magnetic head slider |
JPH062617B2 (en) * | 1986-06-25 | 1994-01-12 | ティーディーケイ株式会社 | Ceramic material for magnetic head slider |
JPS638257A (en) * | 1986-06-25 | 1988-01-14 | ティーディーケイ株式会社 | Ceramic material |
JPH062618B2 (en) * | 1986-06-26 | 1994-01-12 | ティーディーケイ株式会社 | Ceramic material for magnetic head slider |
JPS638258A (en) * | 1986-06-26 | 1988-01-14 | ティーディーケイ株式会社 | Ceramic material |
JPH02157206A (en) * | 1988-12-08 | 1990-06-18 | Kureha Chem Ind Co Ltd | Dental adhesive |
JPH076537A (en) * | 1993-04-22 | 1995-01-10 | Tdk Corp | Slider for magnetic head device and production of this slider |
US6590745B1 (en) | 1999-01-26 | 2003-07-08 | Tdk Corporation | Magnetic head, method of manufacturing same, and magnetic disk apparatus |
US7056961B2 (en) | 2000-12-04 | 2006-06-06 | Tokuyama Corporation | Adhesive composition for denture base relining material and dental curable composition |
JP2009504350A (en) * | 2005-08-18 | 2009-02-05 | デンツプライ インターナショナル インコーポレーテッド | Adhesive and method for gluing artificial plastic teeth |
WO2008019978A2 (en) * | 2006-08-16 | 2008-02-21 | Ivoclar Vivadent Ag | Pasty, polymerizable dental compounds and method for producing the same |
WO2008019978A3 (en) * | 2006-08-16 | 2008-12-11 | Ivoclar Vivadent Ag | Pasty, polymerizable dental compounds and method for producing the same |
US8436070B2 (en) | 2006-08-16 | 2013-05-07 | Ivoclar Vivadent Ag | Pasty polymerizable dental compounds and method for producing the same |
Also Published As
Publication number | Publication date |
---|---|
JPH0447642B2 (en) | 1992-08-04 |
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