JPH0227961B2 - - Google Patents
Info
- Publication number
- JPH0227961B2 JPH0227961B2 JP59200469A JP20046984A JPH0227961B2 JP H0227961 B2 JPH0227961 B2 JP H0227961B2 JP 59200469 A JP59200469 A JP 59200469A JP 20046984 A JP20046984 A JP 20046984A JP H0227961 B2 JPH0227961 B2 JP H0227961B2
- Authority
- JP
- Japan
- Prior art keywords
- composition
- inlay
- acid ester
- methacrylic acid
- denture
- 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
Links
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 24
- 239000000178 monomer Substances 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 13
- 125000005397 methacrylic acid ester group Chemical group 0.000 claims description 11
- 235000012239 silicon dioxide Nutrition 0.000 claims description 10
- 239000000377 silicon dioxide Substances 0.000 claims description 10
- 239000011342 resin composition Substances 0.000 claims description 9
- 150000001451 organic peroxides Chemical class 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 7
- 238000000465 moulding Methods 0.000 claims description 3
- 239000000049 pigment Substances 0.000 description 6
- 238000001723 curing Methods 0.000 description 5
- 208000002925 dental caries Diseases 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 239000004342 Benzoyl peroxide Substances 0.000 description 4
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 4
- 235000019400 benzoyl peroxide Nutrition 0.000 description 4
- 239000011505 plaster Substances 0.000 description 4
- AMFGWXWBFGVCKG-UHFFFAOYSA-N Panavia opaque Chemical compound C1=CC(OCC(O)COC(=O)C(=C)C)=CC=C1C(C)(C)C1=CC=C(OCC(O)COC(=O)C(C)=C)C=C1 AMFGWXWBFGVCKG-UHFFFAOYSA-N 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000004926 polymethyl methacrylate Substances 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000012756 surface treatment agent Substances 0.000 description 3
- XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 description 2
- 229910002012 Aerosil® Inorganic materials 0.000 description 2
- 229910000497 Amalgam Inorganic materials 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 239000003479 dental cement Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 description 1
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- JUDXBRVLWDGRBC-UHFFFAOYSA-N [2-(hydroxymethyl)-3-(2-methylprop-2-enoyloxy)-2-(2-methylprop-2-enoyloxymethyl)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(CO)(COC(=O)C(C)=C)COC(=O)C(C)=C JUDXBRVLWDGRBC-UHFFFAOYSA-N 0.000 description 1
- SWHLOXLFJPTYTL-UHFFFAOYSA-N [2-methyl-3-(2-methylprop-2-enoyloxy)-2-(2-methylprop-2-enoyloxymethyl)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(C)(COC(=O)C(C)=C)COC(=O)C(C)=C SWHLOXLFJPTYTL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000004851 dental resin Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000010794 food waste Substances 0.000 description 1
- 239000005350 fused silica glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 210000000214 mouth Anatomy 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920001483 poly(ethyl methacrylate) polymer Polymers 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- HQYALQRYBUJWDH-UHFFFAOYSA-N trimethoxy(propyl)silane Chemical compound CCC[Si](OC)(OC)OC HQYALQRYBUJWDH-UHFFFAOYSA-N 0.000 description 1
- -1 γ-methacryloxy Substances 0.000 description 1
Landscapes
- Adhesives Or Adhesive Processes (AREA)
- Dental Preparations (AREA)
- Dental Prosthetics (AREA)
- Polymerisation Methods In General (AREA)
- Graft Or Block Polymers (AREA)
Description
産業上の利用分野
本発明は歯科用硬質レジン組成物をインレー体
及び義歯床の製作に使用する方法に関する。
従来の技術
歯のう蝕部を削除した窩洞に充填する従来のイ
ンレー体には、コンポジツト、銀アマルガム、金
属などがある。コンポジツトは破砕抗力が低く、
また充填した窩洞から離脱することが多い。この
原因は窩洞と充填物との間に空隙があるためであ
る。従つて充填後短期間に水分及び食物残渣が入
り、また残留モノマーが残つているため二次的カ
リエスを生じた症例が現在多くの学者から報告さ
れている。銀アマルガム及び金属はその色調が自
然の歯との違和感を生じ、美感を損なう欠点があ
る。また、金属インレー体の製作には、ワツクス
パターンを作り、埋没材などを使用した金属を鋳
造し、さらに研摩を行うため、成形に長時間を要
する。
また、従来の義歯床は、メタクリル酸エステル
単量体とメタクリル酸エステル重合体及び顔料の
混合物を使用している。この混合物は、硬化さ
せ、また残留モノマーを減少させるために要する
加熱時間が非常に長い。また、成形物の強度は十
分でなく、義歯床のあごに当る部分を金属で形成
することもあり、美感を損ない患者の心理的負担
となる。
発明が解決しようとする問題点
本発明者らは、前に述べた従来のインレー体及
び義歯床がその製作に長時間を要し、かつ強度が
十分でないと云う欠点を改良するために、メタク
リル酸系エステル単量体又はメタクリル酸系エス
テル単量体とその重合体、二酸化ケイ素及び有機
過酸化物からなる歯科用硬質レジン組成物を使用
し、その硬化成形に2000〜3000MHzのマイクロ
波を使用して問題点を解決しようとするものであ
る。
問題点を解決するための手段
本発明に使用する歯科用硬質レジン組成物は、
メタクリル酸系エステル単量体30〜70重量%、メ
タクリル酸系エステル重合体0〜30重量%、二酸
化ケイ素30〜70重量%、有機過酸物0.3〜3.5重量
%、さらに二酸化ケイ素表面処理剤0〜5重量%
を加えることもでき、また必要によつては患者の
自然歯と同じ色調にするために顔料を少量混合す
ることもできる。
メタクリル酸系エステル単量体としては、例え
ばビスフエノールAグリシジルメタクリレート
(以下BisGMAを略称する)、トリエチレングリ
コール.ジメタクリレート(以下3Gと略称す
る)、2・2ビス
INDUSTRIAL APPLICATION FIELD OF THE INVENTION The present invention relates to a method of using a dental hard resin composition in the production of inlay bodies and denture bases. BACKGROUND OF THE INVENTION Conventional inlay materials for filling cavities from tooth cavities include composites, silver amalgams, and metals. Composites have low crushing drag;
They also often separate from the filled cavity. This is because there is a gap between the cavity and the filling. Therefore, many scholars are currently reporting cases in which secondary caries occurred due to moisture and food residue entering the container within a short period of time after filling, and residual monomer remaining. Silver amalgam and metals have the disadvantage that their color tone does not match natural teeth and impairs their aesthetic appearance. Furthermore, in order to manufacture a metal inlay body, a wax pattern is created, metal is cast using an investment material, etc., and further polishing is performed, so it takes a long time to form the body. Additionally, conventional denture bases use a mixture of methacrylate monomers, methacrylate polymers, and pigments. This mixture requires very long heating times to cure and reduce residual monomer. Furthermore, the strength of the molded product is not sufficient, and the portion of the denture base that touches the jaw may be made of metal, which impairs the aesthetic appearance and places a psychological burden on the patient. Problems to be Solved by the Invention In order to improve the drawbacks that the conventional inlay bodies and denture bases mentioned above require a long time to manufacture and do not have sufficient strength, the present inventors have developed a methacrylic material. A dental hard resin composition consisting of an acid ester monomer or methacrylic acid ester monomer and its polymer, silicon dioxide, and an organic peroxide is used, and microwaves of 2000 to 3000 MHz are used for curing and molding. This is an attempt to solve the problem. Means for Solving the Problems The dental hard resin composition used in the present invention is
30-70% by weight of methacrylic acid ester monomer, 0-30% by weight of methacrylic ester polymer, 30-70% by weight of silicon dioxide, 0.3-3.5% by weight of organic peroxide, and 0 silicon dioxide surface treatment agent. ~5% by weight
or, if necessary, a small amount of pigment may be mixed in to match the color of the patient's natural teeth. Examples of methacrylic acid ester monomers include bisphenol A glycidyl methacrylate (hereinafter abbreviated as BisGMA), triethylene glycol. Dimethacrylate (hereinafter abbreviated as 3G), 2.2 bis
【4−(メタクロキシエトキシ)
フエニール】プロパン(以下D−2・6Eと略称
する)、ポリメチルメタクリレート、ジエチレン
グリコールジメタクリレート、テトラメチロール
トリアクリレート、テトラメチロールメタントリ
メタクリレート、トリメチロールエタントリメタ
クリレート、メチルメタクリレートなどを使用す
ることができる。
メタクリル酸エステル重合体としては、ポリメ
チルメタクリレート、ポリエチルメタクリレート
及び前記メタクリル酸系エステル単量体の重合体
及び共重合体などを使用することができる。
二酸化ケイ素としては、γ−メタクリロキシ・
プロピルトリメトキシシランで表面処理を行なつ
た石英粉末、アモルフアストシリカ(アエロジル
社製)などを使用することができる。また、表面
処理剤としては、γ−メタクリロキシ・プロピル
トリメトキシシランなどのシランカツプリング剤
を使用することができる。二酸化ケイ素は組成物
をペースト状にするため及び形成されたインレー
体及び義歯床に硬度と強度を与えるためである。
有機過酸化物としては、例えば過酸化ベンゾイ
ルが使用される。メタクリル酸系エステル単量体
だけを2000〜3000MHzの高周波数(以下マイク
ロ波と称す)で処理するときは、硬化した樹脂の
表面が未反応の状態である。有機過酸化物を混合
した組成物は樹脂化が完全に行なわれる。これは
マイクロ波による発熱作用とその熱によつて有機
過酸化物が分解して生成する活性ラジカルの作用
によつて重合硬化反応がより強力に行なわれるた
めと思われる。
本発明に使用する前記歯科用硬質レジン組成物
は、マイクロ波によつて発熱し、厚めの組成物で
も数分間で完全に重合硬化し、強度の大きな成形
物を与える。
次に、前記歯科用硬質レジン組成物をインレー
体に使用する方法は、う蝕部を削除した歯牙の印
象を採得し、この印象から石こう模型を作り、そ
の上に前記組成物のインレー体を形成し、マイク
ロ波で数分間処理して組成物を硬化させる。硬化
したインレー体を歯牙の窩洞に歯科セメントで合
着させる。
インレー体に使用する従来のコンポジツトは、
硬化1時間半後に測定した破砕抗力が215Kgf/
cm2であるが、本発明の方法のインレー体の5分間
マイクロ波で処理したときの破砕抗力は300Kg
f/cm2であり、残留モノマーがない。また、本発
明の方法で窩洞に合着したインレー体は、脱落す
ることがなく、また組成物に顔料を混合して患者
の自然歯の色調と同じように調整できるので、美
感を損なうことがない。さらに、本発明の方法に
よるインレー体は短時間で作ることができる。
次に、前記組成物を義歯床に使用する方法は、
治療する部分の印象を採得し、それによつて石こ
う模型を作り、その上に患者の歯茎及びあご部分
の色調になるように顔料を混合した組成物で義歯
床を形成し、義歯床形成のろう堤部分に適当な義
歯を固定してマイクロ波で数分間処理して義歯を
装着した強固な義歯床が作られる。本発明の方法
による義歯床は強度が大きいのでそのあご部分も
比較的薄く形成することができ、かつ軽量であ
り、義歯床を口腔に装着したときの感触もよい。
次に実施例によつて本発明の組成物及びその使
用方法を説明する。
実施例 1
重量部
BisGMA 70
3G 30
溶融シリカ粉末(10μ以下) 100
ポリメチルメタクリレート(50μ以下) 50
過酸化ベンゾイル 1
インレー体の場合は、上記組成に1重量部の顔
料を混合しペースト状組成物を製造した。う蝕部
を削除した歯牙の印象を採得し、この印象から石
こう模型を作り、前記組成物を窩洞に充填し、電
子レジン中マイクロ波で5分間処理してインレー
体を作つた。このインレー体は歯の窩洞に歯科セ
メントで合着するとき、自然歯と同じ色調で、し
かも窩洞に強固に合着されていた。
義歯床の場合は上記組成に2重量部の顔料を混
合しペースト状組成物を製造した。治療する部分
の印象を採得し、それによつて石こう模型を作
り、その上に前記組成物を填入して義歯床を形成
し、義歯床のろう堤部分に義歯を固定し、電子レ
ンジ中マイクロ波で7分間理して義歯を強固に保
持した、強度の大きい義歯床が得られた。
実施例 2
重量部
D−2・6E 70
3G 30
過酸化ベンゾイル 1
石英(シラン処理剤のもの) 200
表面処理剤 1
上記組成物を使用し、実施例1と同様にインレ
ー体及び義歯床を製作した。いずれの場合も従来
のものと比較して強度が大きく、美感を損なわな
いものが得られた。
実施例 3
重量部
D−2・6E 70
3G 30
過酸化ベンゾイル 1
アモルフアストシリカ(アエロジル社製R972)
100
上記組成の組成物を使用し、実施例1と同様に
インレー体及び義歯床を製作した。いずれの場合
も従来のものと比較して強度が大きく、美感を損
なわないものが得られた。
発明の効果
本発明の歯科用硬質レジン組成物の使用方法
は、従来のフラスコ法や重合釜を使用する硬化法
あるいはその他の加熱重合法による硬化物と比較
して、マイクロ波を使用して短時間で完全に硬化
することができて、しかも機械的及び物理的性質
が従来のものより優れた硬化物が得られる。従つ
て、前記硬質レジン組成物を使用し、インレー体
及び義歯床の製作工程において組成物の硬化にマ
イクロ波を使用するので、製作装置として家庭用
電子レンジの使用が可能で安価であり、また製作
時間が短く、しかも強度が大きく、美感を損なわ
ない製作物が得られる。
追加の関係
原特許第1469528号(特公昭63−17804)の発明
は、アクリル系モノマー、二酸化ケイ素及び有機
過酸化物からなる歯科用硬質レジン組成物を義歯
の形成に使用する際、該組成物をマイクロ波で処
理して硬化成形する方法に関するものである。本
発明もメタクリル酸系エステル単量体又はメタク
リ酸系エステル単量とその重合体、二酸化ケイ素
及び有機過酸化物からなる組成物をマイクロ波を
使用して硬化することをその主要部として、該組
成物をインレー体及び義歯床の製作に使用するも
のであつて、特許法第31条第1項に該当するもの
である。[4-(Methacroxyethoxy)
Phenyl] propane (hereinafter abbreviated as D-2.6E), polymethyl methacrylate, diethylene glycol dimethacrylate, tetramethylol triacrylate, tetramethylolmethane trimethacrylate, trimethylolethane trimethacrylate, methyl methacrylate, etc. can be used. As the methacrylic acid ester polymer, polymethyl methacrylate, polyethyl methacrylate, polymers and copolymers of the above-mentioned methacrylic acid ester monomers, etc. can be used. As silicon dioxide, γ-methacryloxy,
Quartz powder surface-treated with propyltrimethoxysilane, amorphous asto silica (manufactured by Aerosil), etc. can be used. Further, as a surface treatment agent, a silane coupling agent such as γ-methacryloxypropyltrimethoxysilane can be used. The silicon dioxide is used to make the composition into a paste and to provide hardness and strength to the formed inlay and denture base. As the organic peroxide, for example, benzoyl peroxide is used. When only the methacrylic acid ester monomer is treated with a high frequency of 2000 to 3000 MHz (hereinafter referred to as microwave), the surface of the cured resin remains unreacted. A composition mixed with an organic peroxide is completely converted into a resin. This is thought to be because the polymerization curing reaction is carried out more strongly due to the exothermic action of microwaves and the action of active radicals generated by the decomposition of the organic peroxide by the heat. The dental hard resin composition used in the present invention is heated by microwaves, and even thick compositions are completely polymerized and cured in several minutes, giving molded products with high strength. Next, the method of using the dental hard resin composition for an inlay body is to take an impression of a tooth with caries removed, make a plaster model from this impression, and then place an inlay body of the composition on it. and cure the composition by microwave treatment for several minutes. The hardened inlay body is bonded to the tooth cavity with dental cement. Traditional composites used for inlay bodies are
The crushing force measured after 1 and a half hours of curing was 215Kgf/
cm2 , but the crushing force of the inlay body according to the method of the present invention when treated with microwaves for 5 minutes is 300Kg.
f/cm 2 and there is no residual monomer. Furthermore, the inlay body adhered to the cavity by the method of the present invention does not fall off, and the color tone can be adjusted to match the patient's natural teeth by mixing pigments in the composition, so the aesthetic appearance will not be impaired. do not have. Furthermore, inlay bodies according to the method of the invention can be produced in a short time. Next, the method of using the composition for a denture base is as follows:
An impression of the area to be treated is taken, a plaster model is made from the impression, and a denture base is formed on the impression with a pigment mixed to match the color of the patient's gums and jaw area. A suitable denture is fixed to the wax ridge and treated with microwaves for several minutes to create a strong denture base to which the denture is attached. Since the denture base produced by the method of the present invention has high strength, the jaw portion thereof can be formed relatively thin, is lightweight, and has a good feel when attached to the oral cavity. The composition of the present invention and its method of use will now be explained by way of examples. Example 1 Parts by weight BisGMA 70 3G 30 Fused silica powder (10μ or less) 100 Polymethyl methacrylate (50μ or less) 50 Benzoyl peroxide 1 For an inlay body, 1 part by weight of pigment is mixed with the above composition to form a paste composition. was manufactured. An impression of the tooth with the carious area removed was taken, a plaster model was made from this impression, the cavity was filled with the composition, and the inlay body was prepared by treating with microwaves in an electronic resin for 5 minutes. When this inlay body was bonded to the tooth cavity with dental cement, it had the same color as a natural tooth and was firmly bonded to the cavity. In the case of a denture base, 2 parts by weight of pigment was mixed with the above composition to produce a paste composition. An impression of the area to be treated is taken, a plaster model is made based on the impression, the composition is placed thereon to form a denture base, the denture is fixed to the wax ridge part of the denture base, and the denture is placed in a microwave oven. After 7 minutes of microwaving, a strong denture base that firmly held the denture was obtained. Example 2 Parts by weight D-2・6E 70 3G 30 Benzoyl peroxide 1 Quartz (silane treatment agent) 200 Surface treatment agent 1 Using the above composition, an inlay body and a denture base were manufactured in the same manner as in Example 1. did. In all cases, products were obtained that had greater strength than conventional products and did not impair aesthetic appearance. Example 3 Parts by weight D-2・6E 70 3G 30 Benzoyl peroxide 1 Amorphous asto silica (R972 manufactured by Aerosil)
100 An inlay body and a denture base were manufactured in the same manner as in Example 1 using the composition having the above composition. In all cases, products were obtained that had greater strength than conventional products and did not impair aesthetic appearance. Effects of the Invention The dental hard resin composition of the present invention can be used in a shorter period of time using microwaves, compared to the conventional curing method using a flask method, a polymerization pot, or other heat polymerization methods. The cured product can be completely cured in a short period of time and has better mechanical and physical properties than conventional products. Therefore, since the above-mentioned hard resin composition is used and microwaves are used to harden the composition in the manufacturing process of the inlay body and denture base, it is possible to use a household microwave oven as a manufacturing device, and it is inexpensive. It is possible to obtain a product that takes less time to produce, has greater strength, and does not impair its aesthetic appearance. Additional Relationships The invention of original patent No. 1469528 (Japanese Patent Publication No. 17804/1986) provides that when a hard dental resin composition comprising an acrylic monomer, silicon dioxide, and an organic peroxide is used for forming dentures, This relates to a method of curing and molding by treating with microwaves. The main part of the present invention is to cure a composition consisting of a methacrylic acid ester monomer or a methacrylic acid ester monomer and its polymer, silicon dioxide, and an organic peroxide using microwaves. The composition is used for manufacturing inlay bodies and denture bases, and falls under Article 31, Paragraph 1 of the Patent Law.
Claims (1)
ル酸系エステル単量体とメタクリル酸系エテル重
合体、二酸化ケイ素及び有機過酸化物からなる歯
科用硬質レジン組成物をインレー体及び義歯床の
製作に使用する工程中において前記組成物を2000
〜3000MHzの高周波数のマイクロ波で硬化成形
することを特徴とする歯科用硬質レジン組成物の
使用方法。1. A dental hard resin composition consisting of a methacrylic acid ester monomer or a methacrylic acid ester monomer, a methacrylic acid ester polymer, silicon dioxide, and an organic peroxide is used in the production of inlay bodies and denture bases. During the process, the composition is
A method of using a dental hard resin composition characterized by curing and molding with microwaves at a high frequency of ~3000MHz.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59200469A JPS6178707A (en) | 1984-09-27 | 1984-09-27 | Easily processable hard resin composition for dental use, and its use |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59200469A JPS6178707A (en) | 1984-09-27 | 1984-09-27 | Easily processable hard resin composition for dental use, and its use |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6178707A JPS6178707A (en) | 1986-04-22 |
| JPH0227961B2 true JPH0227961B2 (en) | 1990-06-20 |
Family
ID=16424833
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59200469A Granted JPS6178707A (en) | 1984-09-27 | 1984-09-27 | Easily processable hard resin composition for dental use, and its use |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6178707A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6335508A (en) * | 1986-07-31 | 1988-02-16 | G C Dental Ind Corp | Resin composition for denture base |
| CN102973416B (en) * | 2012-12-07 | 2014-07-23 | 东华大学 | Preparation method of dental restoring resin taking silicon dioxide and cluster of silicon dioxide as stuffing |
-
1984
- 1984-09-27 JP JP59200469A patent/JPS6178707A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6178707A (en) | 1986-04-22 |
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