JPS5856741B2 - Metal mixed powder for mercury amalgam as dental filling material - Google Patents

Metal mixed powder for mercury amalgam as dental filling material

Info

Publication number
JPS5856741B2
JPS5856741B2 JP54152486A JP15248679A JPS5856741B2 JP S5856741 B2 JPS5856741 B2 JP S5856741B2 JP 54152486 A JP54152486 A JP 54152486A JP 15248679 A JP15248679 A JP 15248679A JP S5856741 B2 JPS5856741 B2 JP S5856741B2
Authority
JP
Japan
Prior art keywords
powder
amalgam
filling material
alloy
mixed powder
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
Application number
JP54152486A
Other languages
Japanese (ja)
Other versions
JPS5677213A (en
Inventor
慶三郎 宮田
宏 大谷
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.)
GIFU SHIKA DAIGAKU
Original Assignee
GIFU SHIKA DAIGAKU
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 GIFU SHIKA DAIGAKU filed Critical GIFU SHIKA DAIGAKU
Priority to JP54152486A priority Critical patent/JPS5856741B2/en
Publication of JPS5677213A publication Critical patent/JPS5677213A/en
Publication of JPS5856741B2 publication Critical patent/JPS5856741B2/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K6/00Preparations for dentistry
    • A61K6/80Preparations for artificial teeth, for filling teeth or for capping teeth
    • A61K6/84Preparations for artificial teeth, for filling teeth or for capping teeth comprising metals or alloys
    • A61K6/847Amalgams

Landscapes

  • Health & Medical Sciences (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Plastic & Reconstructive Surgery (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Powder Metallurgy (AREA)
  • Dental Preparations (AREA)

Description

【発明の詳細な説明】 本発明は歯科医療の一方法として、いわゆる虫歯のよう
な欠陥の治療に対して、一般に行なわれている金属粉末
を水銀(Hg、)で練ったいわゆるアマルガムを作って
、それを欠陥部に充填する方法に用いる金属材料の改善
にかかるものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention is a method of dental care, in which a so-called amalgam is made by kneading metal powder with mercury (Hg), which is commonly used for the treatment of defects such as cavities. The present invention relates to an improvement in the metal material used in the method of filling defective parts with the metal material.

従来、このアマルガムに用いる金属材料は、AgとSn
を主体とする一種類の合金粉末に対し、数10饅のHg
を添加して用いる方法が長らく行なわれてきたが、実際
治療に用いてみると種々の欠点がある。
Conventionally, the metal materials used for this amalgam are Ag and Sn.
For one type of alloy powder mainly composed of
The method of adding and using it has been practiced for a long time, but when used in actual treatment, there are various drawbacks.

すなわち、アマルガム充填体の端部が破損し易いとか、
腐蝕し易いなどの欠点があり、いろいろの改良が行なわ
れてきたが、末だ不完全である。
In other words, the edges of the amalgam filling are easily damaged,
It has drawbacks such as being easily corroded, and although various improvements have been made, it remains incomplete.

これを実例について述べる。1929年アメリカにおい
てはAgとSnを主体とする合金の規格を下記のように
定めた。
This will be explained using an example. In 1929, the United States established the following specifications for alloys mainly composed of Ag and Sn.

すなわち、Ag65饅以上、5n29%以下、Cu6%
以下、Zn 2φ以下とし、これらの元素を溶解して作
製した合金粉末に対し、数10%のHgを加えてアマル
ガムとするものである。
That is, Ag65 or more, 5n29% or less, Cu6%
Hereinafter, several 10% of Hg is added to an alloy powder prepared by melting Zn and these elements to obtain an amalgam.

この規格で作製したアマルガム充填物は噛合せに必要な
圧縮強度が弱く、且つr2相と称する金属間化合物が析
出して腐蝕し易い。
Amalgam fillings made according to this standard have a weak compressive strength required for interlocking, and are susceptible to corrosion due to the precipitation of an intermetallic compound called the r2 phase.

これを改善するため、1963年カナダにおいて、上記
アメリカ規格の合金粉末に対し、別にAg Cu二元
系合金(60at%Ag)の粉末を作って、これを20
%前後混合し、この二種の合金粉末混合物に数10%の
Hgを加えて練るアマルガム材料が発売され、実用に供
されているが、このアマルガムは、r2相は析出しない
が、かわりにAg−Cu合金粒の表面に新たにCu6S
n5なる金属間化合物ができ、これが新たなる腐蝕の原
因となることがわかった。
In order to improve this, in Canada in 1963, a separate Ag-Cu binary alloy (60at%Ag) powder was made in addition to the above-mentioned American standard alloy powder, and this was
An amalgam material made by adding several tens of percent of Hg to a mixture of these two types of alloy powder and kneading it has been released and is in practical use. -Cu6S newly added to the surface of Cu alloy grains
It was found that an intermetallic compound called n5 was formed and this was a new cause of corrosion.

また、この混合物によるアマルガムは、従来の一種類の
合金によるものよりかえって圧縮強度が10饅低下する
ことがわかった。
It was also found that the compressive strength of the amalgam made from this mixture was 10 times lower than that of the conventional amalgam made from a single type of alloy.

しかし、r2相の析出がなくなった点は注目すべきであ
る。
However, it is noteworthy that the precipitation of r2 phase disappeared.

本発明は上記の歴史的発展の過程を詳細に検討し、従来
のアマルガム用合金による欠点を総て除去し、強度も強
く、対軸性の優れたアマルガム材を完成したものである
The present invention has been made by studying the above historical development process in detail, and has completed an amalgam material that eliminates all the drawbacks of conventional amalgam alloys, has strong strength, and has excellent anti-axial properties.

これを実施の一例について述べる。An example of implementing this will be described.

Ag52%、Sn 27.5%、Cu 18.5%、Z
n1%、In1%の合金粉末を作り、これに電解Ag粉
末10%を混合して、この混合粉末に対し、 Hgを数
10%加えてアマルガムとした。
Ag52%, Sn 27.5%, Cu 18.5%, Z
An alloy powder containing 1% N and 1% In was prepared, and 10% electrolytic Ag powder was mixed therein, and several 10% Hg was added to this mixed powder to form an amalgam.

こうしてできた混合粉末によってアマルガムとした場合
、その反応生成物は、rl 相(Ag2Hg5 )と若
干のCu6 Sn5相ができる外に、新たにβ1相(A
gHg)なる金属化合物ができることがわかった。
When amalgam is made from the mixed powder thus produced, the reaction product not only forms rl phase (Ag2Hg5) and some Cu6Sn5 phase, but also newly forms β1 phase (Ag2Hg5).
It was found that a metal compound called gHg) can be formed.

この新たにできたβ1相は従来のいかなるアマルガムで
も現出させることのできなかったものであるが、このβ
1相(AgHg)はr1相(Ag2Hg5 )に原子比
も近く、未反応のままアマルガム中の核となっているr
相(A g 3 S n )と結晶構造は極めて近似
しており、両者は一次的に結合し易く、Hg中に分散し
ている粒子を結合させる性質をもっており、β1相の無
いものより衝撃強度が著しく向上し、耐蝕性も著しく向
上する。
This newly formed β1 phase could not be made to appear in any conventional amalgam;
Phase 1 (AgHg) has a close atomic ratio to phase r1 (Ag2Hg5), and r remains unreacted and forms the nucleus in the amalgam.
The phase (A g 3 S n ) and the crystal structure are extremely similar, and the two are easily combined in a primary manner, and have the property of binding particles dispersed in Hg, resulting in higher impact strength than those without the β1 phase. is significantly improved, and corrosion resistance is also significantly improved.

この事実は次の実験の結果により明らかである。This fact is clear from the results of the following experiment.

上記混合物粉末にHgを数10多混和し、20秒間練和
したる後、18kgで加圧しくADA規格試験法)、直
径4.772.長さ8朋の円柱形試片を作製した。
Several dozen pieces of Hg were mixed into the above powder mixture, kneaded for 20 seconds, and then pressurized with 18 kg (ADA standard test method), diameter 4.772. A cylindrical specimen with a length of 8 mm was prepared.

円柱試料作製後、1時間後の圧縮強度は1610 kg
/fflで、ADA規格の815.5 kg/crit
からみて約2倍の強大な値を示している。
The compressive strength after 1 hour after preparing the cylindrical sample was 1610 kg.
/ffl, 815.5 kg/crit of ADA standard
This shows a value that is approximately twice as strong.

練和後3日後では実に4500 kg/C1?Lとなり
、極めて優れていることがわかった。
4500 kg/C1 after 3 days of kneading? It was found to be extremely excellent.

また、ADA規格の46.3−荷重の加圧試験よりも更
にきびしい60kg加圧を行ってクリープ値を求めたと
ころ、0.11%となり、46.3kg加圧で要求され
る5φ以下からみて極めてすぐれていることが明らかと
なった。
In addition, when the creep value was determined by applying 60 kg of pressure, which is even more severe than the ADA standard 46.3-load pressurization test, it was 0.11%, which is less than 5φ required for 46.3 kg of pressurization. It turned out to be extremely good.

耐蝕性試験では、Ag粉末の量を増すと、Cu6Sn5
相からの緑青色の腐蝕色は減少し、10φAgではゾ完
全に阻止することができた。
In the corrosion resistance test, increasing the amount of Ag powder caused Cu6Sn5
The green-blue corrosion color from the phase was reduced and could be completely inhibited with 10φAg.

このように機械的性質および耐蝕性において、本発明は
理想的なアマルガム用金属混合粉末を完成したもので、
特許請求範囲に記述した各元素の組成範囲はこれらの機
械的および電気化学的性質において許容し得る最低値と
最高値を示したものである。
In this way, the present invention has completed the ideal metal mixed powder for amalgam in terms of mechanical properties and corrosion resistance.
The composition ranges of each element described in the claims indicate the minimum and maximum allowable values of these mechanical and electrochemical properties.

なお本願発明において、Inは合金結晶粒を微細化する
作用を奏する。
In the present invention, In has the effect of refining alloy crystal grains.

またZnは、合金を溶解する時に選択的に酸素と結合し
た合金溶湯表面を酸化亜鉛の皮膜で被い、Ag 、Sn
、Cuの酸化を防止し、これらAg 、 S n。
In addition, when Zn is melted, the surface of the molten alloy selectively combined with oxygen is covered with a film of zinc oxide, and Ag, Sn
, prevents the oxidation of Cu, and these Ag, Sn.

Cuの成分比の変動を防止する作用を奏する。This has the effect of preventing fluctuations in the Cu component ratio.

以上のごとく本発明は従来求めて為し得なかった理想的
アマルガム用金属混合粉を完成したもので、工業的価値
極めて犬である。
As described above, the present invention has completed an ideal metal mixed powder for amalgam, which has not been achieved in the past, and has extremely high industrial value.

Claims (1)

【特許請求の範囲】 1 合金組成としてAg45φ〜65%、5n20%〜
30%、cu1o%〜25φをもって構成されたる合金
の粉末を作製し、この合金粉末に対し電解Ag粉末のよ
うな純Ag粉末を5φ〜25多混合して成る歯科充填材
料としての水銀アマルガム用金属混合粉末。 2 合金組成としてAg45%〜65%、5n20%〜
30%、CulO%〜25%、Zn2%以下、In3%
以下をもって構成されたる合金の粉末を作製し、この合
金粉末に対し電解Ag粉末のような純Ag粉末を5%〜
25饅混合して成る歯科充填材としての水銀アマルガム
用金属混合粉末。
[Claims] 1. Alloy composition: Ag45φ~65%, 5n20%~
A metal for mercury amalgam as a dental filling material, which is prepared by preparing an alloy powder having a diameter of 30%, cu1o% to 25φ, and mixing pure Ag powder such as electrolytic Ag powder with 5φ to 25φ to this alloy powder. Mixed powder. 2 Alloy composition: Ag45%~65%, 5N20%~
30%, CulO% ~ 25%, Zn 2% or less, In 3%
Create an alloy powder composed of the following, and add 5% to pure Ag powder such as electrolytic Ag powder to this alloy powder.
A metal mixed powder for mercury amalgam as a dental filling material, which is made by mixing 25 pieces of powder.
JP54152486A 1979-11-27 1979-11-27 Metal mixed powder for mercury amalgam as dental filling material Expired JPS5856741B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP54152486A JPS5856741B2 (en) 1979-11-27 1979-11-27 Metal mixed powder for mercury amalgam as dental filling material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP54152486A JPS5856741B2 (en) 1979-11-27 1979-11-27 Metal mixed powder for mercury amalgam as dental filling material

Publications (2)

Publication Number Publication Date
JPS5677213A JPS5677213A (en) 1981-06-25
JPS5856741B2 true JPS5856741B2 (en) 1983-12-16

Family

ID=15541526

Family Applications (1)

Application Number Title Priority Date Filing Date
JP54152486A Expired JPS5856741B2 (en) 1979-11-27 1979-11-27 Metal mixed powder for mercury amalgam as dental filling material

Country Status (1)

Country Link
JP (1) JPS5856741B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3290908A1 (en) 2016-09-06 2018-03-07 Hitachi High-Tech Science Corporation Unknown sample determining method, unknown sample determining instrument, and unknown sample determining program
WO2020262534A1 (en) * 2019-06-26 2020-12-30 旭化成メディカル株式会社 Concentration calculation device and blood treatment system

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3290908A1 (en) 2016-09-06 2018-03-07 Hitachi High-Tech Science Corporation Unknown sample determining method, unknown sample determining instrument, and unknown sample determining program
WO2020262534A1 (en) * 2019-06-26 2020-12-30 旭化成メディカル株式会社 Concentration calculation device and blood treatment system

Also Published As

Publication number Publication date
JPS5677213A (en) 1981-06-25

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