JPS6312042B2 - - Google Patents
Info
- Publication number
- JPS6312042B2 JPS6312042B2 JP53154370A JP15437078A JPS6312042B2 JP S6312042 B2 JPS6312042 B2 JP S6312042B2 JP 53154370 A JP53154370 A JP 53154370A JP 15437078 A JP15437078 A JP 15437078A JP S6312042 B2 JPS6312042 B2 JP S6312042B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- coupling agent
- silane coupling
- silicic acid
- dental
- 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
Links
Landscapes
- Dental Preparations (AREA)
Description
〔産業上の利用分野〕
本発明は、歯科用合成樹脂の充填材、特に歯の
欠損部の補修用合成樹脂に配合する充填材に関す
る。
〔従来の技術〕
従来から、歯科用補修材としては金,銀,アマ
ルガムなどの金属材料、シリケートセメント,リ
ン酸亜鉛セメント,けいリン酸セメントなどの無
機材料,さらにはポリメチルメタクリレート,グ
リシジルメタクリレート,ポリメチルメタクリレ
ート,メチルメタクリレート,ビスフエノールA
などのプラスチツクに充填材として溶融シリカ,
石英,ガラス,アルミニウムシリケート,セラミ
ツク等の粉末を配合してなるプラスチツク材料な
どが知られている(特開昭53−32994号公報)。
特にプラスチツク材料は、包装、取扱などが容
易であると共に歯の治療においても特別の手段を
必要とすることなく使用出来るので利用価値が高
いが、陶材を焼結成形した陶歯に比べて強度の点
で劣るという欠点があつた。
〔発明が解決しようとする問題点〕
本発明は、以上のプラスチツク材料の強度低下
の欠点を解決し黒色又は黄色などの変色を与える
ことのない充填材を提供することを目的とする。
〔問題点を解決するための手段〕
すなわち、本発明は、ハンター白度が73以上、
SiO299重量%以上、Fe2O30.05重量%以下であつ
て、X線的構造において、α―石英,クリストバ
ライトおよびトリジマイトの反射を示さない溶融
珪酸粉末、またはこれにシランカツプリング剤処
理してなる粉末からなり、しかもその粉末度は
BET法による表面積で1m2/g以上であること
を特徴とする歯科用合成樹脂の充填材である。
本発明の充填材として使用する溶融珪酸は、
SiO2が99重量%以上の高純度であることが必要
であり、またFe2O3は0.05重量%以下である。
Fe2O3が0.05重量%を越えるとプラスチツク材料
が黒色又は黄色等に変色するので好ましくない。
溶融珪酸のX線回折による構造としては、α―
石英,クリストバライトおよびトリジマイト等の
反射が実質的に示さないガラス質のものでなけれ
ば本発明の目的に適合するものとはならない。こ
れらの成分の反射が観察される溶融珪酸であつて
はプラスチツク材料の強度改善はない。
また、本発明に係る溶融珪酸のハンター白度は
73以上である。ハンター白度が73未満のものは、
例えば、ポリメチルメタアクリレート,メチルメ
アクリレート等のプラスチツクと配合した場合、
黒色又は黄色等に変色するので好ましくない。
さらには、本発明の充填材の粉末度はBET法
による表面積が1m2/g以上であることが必要で
ある。1m2/g未満のものをプラスチツクに適量
配合しても歯科用プラスチツク材料の圧縮強度は
2000Kg/cm2以上とならない。その際の粉砕機は特
に制限されるものではないが、不純物の混入しな
いような装置を用いるか、混入したとしても容易
に分離できる手段がとれるものであればよい。具
体的には、振動ミル,ボールミル,スタンプミル
などが用いられるが、ミルのライナーやメデイア
は磁製のもの、コランダム製のものが好都合であ
る。
さらに、シランカツプリング剤処理物を充填材
としてプラスチツクに配合すると、圧縮強度をさ
らに高めることができる。シランカツプリング剤
としては、例えばγ―グリシドキシプロピルトリ
メキシシラン
[Industrial Field of Application] The present invention relates to a dental synthetic resin filling material, particularly to a filling material blended into a synthetic resin for repairing tooth defects. [Prior Art] Traditionally, dental repair materials include metal materials such as gold, silver, and amalgam, inorganic materials such as silicate cement, zinc phosphate cement, and silicate cement, as well as polymethyl methacrylate, glycidyl methacrylate, Polymethyl methacrylate, methyl methacrylate, bisphenol A
Fused silica as a filler in plastics such as
Plastic materials made by blending powders of quartz, glass, aluminum silicate, ceramic, etc. are known (Japanese Patent Laid-Open No. 53-32994). In particular, plastic materials have high utility value as they are easy to package and handle, and can be used in dental treatment without the need for special measures. It had the disadvantage of being inferior in terms of. [Problems to be Solved by the Invention] An object of the present invention is to provide a filler that solves the above-mentioned drawback of reduced strength of plastic materials and does not cause discoloration such as black or yellow. [Means for Solving the Problems] That is, the present invention provides a method for solving problems that
Molten silicic acid powder containing 99% by weight or more of SiO 2 and 0.05% by weight or less of Fe 2 O 3 and whose X-ray structure shows no reflection of α-quartz, cristobalite or tridymite, or treated with a silane coupling agent. It is made of powder of
This dental synthetic resin filling material is characterized by having a surface area of 1 m 2 /g or more as determined by the BET method. The fused silicic acid used as the filler of the present invention is
It is necessary for SiO 2 to have a high purity of 99% by weight or more, and Fe 2 O 3 to be 0.05% by weight or less.
If Fe 2 O 3 exceeds 0.05% by weight, the plastic material will discolor to black or yellow, which is not preferable. The structure of molten silicic acid determined by X-ray diffraction is α-
The purpose of the present invention cannot be met unless the material is glassy, such as quartz, cristobalite, tridymite, etc., which exhibits substantially no reflection. Molten silicic acid, in which reflections of these components are observed, does not improve the strength of plastic materials. Furthermore, the Hunter whiteness of the fused silicic acid according to the present invention is
73 or above. Hunter whiteness is less than 73,
For example, when combined with plastics such as polymethylmethacrylate and methylmethacrylate,
It is not preferable because it discolors to black or yellow. Furthermore, the fineness of the filler of the present invention requires that the surface area measured by the BET method is 1 m 2 /g or more. Even if an appropriate amount of less than 1 m 2 /g is mixed into plastic, the compressive strength of dental plastic material will be
Do not exceed 2000Kg/ cm2 . The pulverizer used in this case is not particularly limited, but any device may be used as long as it does not mix in impurities, or if it does, it can be easily separated. Specifically, a vibrating mill, a ball mill, a stamp mill, etc. are used, and the liner and media of the mill are preferably made of porcelain or corundum. Furthermore, when a treated silane coupling agent is added to plastic as a filler, the compressive strength can be further increased. As a silane coupling agent, for example, γ-glycidoxypropyltrimexysilane
【式】α―(3,4―エポキシシクロ
ヘキシル)エチルトリメトキシシラン
[Formula] α-(3,4-epoxycyclohexyl)ethyltrimethoxysilane
以下、実施例をあげてさらに具体的に説明す
る。
実施例1〜2,比較例1〜8
溶融珪酸および珪石をコランダム製振動ミルで
粉砕して表に示す充填材を製造した。珪酸アルミ
とエアロジルは市販品である。
以上の充填材をシランカツプリング剤で処理し
ないもの、又はγ―グリシドキシプロピルトリメ
トキシシランを主成分としたシランカツプリング
剤の10重量%水溶液をスプレイ法で1重量%添加
し、ブレンダーで1時間表面処理したものをそれ
ぞれ70重量部とポリメチルメタクリレート
(PMMA)30重量部とを配合し硬化させた後に、
その硬化物の圧縮強度の測定と着色状況を肉眼観
察した。
それらの結果を表に示す。
表において圧縮強度の未処理品はシランカツプ
リング剤で処理しない場合の結果であり、処理品
は処理した場合の結果である。また、着色状況
は、未処理品について示したが、処理品も未処理
品とほぼ同じ状況であつた。
Hereinafter, the present invention will be explained in more detail with reference to Examples. Examples 1 to 2, Comparative Examples 1 to 8 Molten silicic acid and silica stone were pulverized using a vibrating mill made of corundum to produce the fillers shown in the table. Aluminum silicate and Aerosil are commercially available products. The above filler is not treated with a silane coupling agent, or 1% by weight of a 10% by weight aqueous solution of a silane coupling agent containing γ-glycidoxypropyltrimethoxysilane as a main component is added by a spray method, and then mixed with a blender. After 1 hour of surface treatment, 70 parts by weight and 30 parts by weight of polymethyl methacrylate (PMMA) were mixed together and cured.
The compressive strength of the cured product was measured and the coloring state was observed with the naked eye. The results are shown in the table. In the table, the compressive strength of untreated products is the result when not treated with a silane coupling agent, and the treated product is the result when treated. Further, although the coloring status is shown for the untreated product, the condition of the treated product was almost the same as that of the untreated product.
【表】【table】
本発明の歯科用合成樹脂の充填材を用いること
により、(1)着色の少ない歯科材料となる、(2)圧縮
強度が高いので、これを用いて歯の治療をすると
丈夫な歯となる、等の効果を奏する。
By using the dental synthetic resin filling material of the present invention, (1) it becomes a dental material with little discoloration, (2) it has high compressive strength, so if you treat your teeth with it, you will have strong teeth. It has the following effects.
Claims (1)
Fe2O30.05重量%以下であつて、X線的構造にお
いて、α―石英、クリストバライトおよびトリジ
マイトの反射を示さない溶融珪酸粉末、またはこ
れにシランカツプリング剤処理をしてなる粉末か
らなり、しかもその粉末度はBET法による表面
積で1m2/g以上であることを特徴とする歯科用
合成樹脂の充填材。1 Hunter whiteness is 73 or more, SiO 2 99% by weight or more,
Consisting of fused silicic acid powder containing 0.05% by weight or less of Fe 2 O 3 and showing no reflection of α-quartz, cristobalite and tridymite in its X-ray structure, or a powder obtained by treating the same with a silane coupling agent, Moreover, the dental synthetic resin filling material is characterized in that its fineness is 1 m 2 /g or more in terms of surface area measured by the BET method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15437078A JPS5579312A (en) | 1978-12-13 | 1978-12-13 | Filler for synthetic resin for dental use |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15437078A JPS5579312A (en) | 1978-12-13 | 1978-12-13 | Filler for synthetic resin for dental use |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5579312A JPS5579312A (en) | 1980-06-14 |
| JPS6312042B2 true JPS6312042B2 (en) | 1988-03-17 |
Family
ID=15582668
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15437078A Granted JPS5579312A (en) | 1978-12-13 | 1978-12-13 | Filler for synthetic resin for dental use |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5579312A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8211407B2 (en) * | 2008-11-25 | 2012-07-03 | The Procter & Gamble Company | Method of making oral care compositions with fused silica slurries |
| CN116283236B (en) * | 2022-12-13 | 2024-09-20 | 潍柴火炬科技股份有限公司 | Alumina ceramic and preparation method and application thereof |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3991008A (en) * | 1974-08-12 | 1976-11-09 | The Kendall Company | Dental compositions having improved color stability |
-
1978
- 1978-12-13 JP JP15437078A patent/JPS5579312A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5579312A (en) | 1980-06-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4294349A (en) | Kit for repair of porcelain dental prostheses | |
| JP2510408B2 (en) | Non glassy micro particles | |
| US4389497A (en) | Use of agglomerates of silicic acid as fillers in dental materials | |
| JP2005517688A (en) | Dental paste, dental article, and method | |
| JPS6183108A (en) | Curable dental restorative material | |
| JP2020152730A (en) | Dental glass, dental composition | |
| Sayyedan et al. | Effect of forsterite nanoparticles on mechanical properties of glass ionomer cements | |
| JP2018507241A (en) | Composite material with ceramic fibers | |
| US8182860B2 (en) | Dental filler | |
| JP2018507241A5 (en) | ||
| JP5068979B2 (en) | Dental filler, method for producing the same, and dental composite material | |
| Lührs et al. | The application of silicon and silicates in dentistry: a review | |
| EP3205327B1 (en) | Sealer composition for root canal filling | |
| JPS6312042B2 (en) | ||
| EP3373887B1 (en) | Kit of parts for producing a glass ionomer cement, process of production and use thereof | |
| US4117595A (en) | Method for repair of porcelain dental prostheses | |
| JP4271800B2 (en) | Dental multifunctional filler | |
| JP3575150B2 (en) | Aluminum hydroxide for resin filling and resin composition using the same | |
| JP7813510B2 (en) | Glass ionomer compositions and methods comprising water-miscible silane-treated nano-sized silica particles. | |
| JP7075635B2 (en) | Dental curable composition | |
| JP2001139843A (en) | Surface modifying filler for dental use | |
| US4256603A (en) | Composition for repair of porcelain dental prostheses | |
| JP7716314B2 (en) | Dental glass ionomer cement composition suitable for mechanical mixing | |
| JP4502673B2 (en) | Filler, composite resin using the filler, and dental prosthesis using the composite resin | |
| CN114306094B (en) | Dental restoration resin composition and preparation method and application thereof |