JPS632521B2 - - Google Patents
Info
- Publication number
- JPS632521B2 JPS632521B2 JP58053800A JP5380083A JPS632521B2 JP S632521 B2 JPS632521 B2 JP S632521B2 JP 58053800 A JP58053800 A JP 58053800A JP 5380083 A JP5380083 A JP 5380083A JP S632521 B2 JPS632521 B2 JP S632521B2
- Authority
- JP
- Japan
- Prior art keywords
- dental
- investment
- gypsum
- aluminum phosphate
- cast
- 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
- 239000000463 material Substances 0.000 claims description 36
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 20
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 claims description 14
- 239000010440 gypsum Substances 0.000 claims description 13
- 229910052602 gypsum Inorganic materials 0.000 claims description 13
- 239000011780 sodium chloride Substances 0.000 claims description 10
- 239000007788 liquid Substances 0.000 claims description 8
- 239000004094 surface-active agent Substances 0.000 claims description 8
- 239000000243 solution Substances 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 11
- 238000004898 kneading Methods 0.000 description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 229910019142 PO4 Inorganic materials 0.000 description 8
- 238000005266 casting Methods 0.000 description 8
- 235000021317 phosphate Nutrition 0.000 description 8
- 229910000623 nickel–chromium alloy Inorganic materials 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 6
- 239000010452 phosphate Substances 0.000 description 6
- 238000007711 solidification Methods 0.000 description 6
- 230000008023 solidification Effects 0.000 description 6
- 230000003746 surface roughness Effects 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000011819 refractory material Substances 0.000 description 4
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229910001316 Ag alloy Inorganic materials 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- 229910001020 Au alloy Inorganic materials 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910001252 Pd alloy Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 229910052925 anhydrite Inorganic materials 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000009933 burial Methods 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- ZOMBKNNSYQHRCA-UHFFFAOYSA-J calcium sulfate hemihydrate Chemical compound O.[Ca+2].[Ca+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O ZOMBKNNSYQHRCA-UHFFFAOYSA-J 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 239000000788 chromium alloy Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 239000003015 dental casting investment Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- OQDJKSVVHFVCAZ-UHFFFAOYSA-H dialuminum;diphosphate Chemical compound [Al+3].[Al+3].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O OQDJKSVVHFVCAZ-UHFFFAOYSA-H 0.000 description 1
- 150000004683 dihydrates Chemical class 0.000 description 1
- 239000003353 gold alloy Substances 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 238000005495 investment casting Methods 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Landscapes
- Dental Preparations (AREA)
Description
本発明は歯科用石膏系埋没材のための練和液に
関するものである。
歯科用埋没材は粉末状であり、水または専用の
練和液で練和して使用される。歯科用埋没材は歯
科補綴物を精密鋳造法によつて製作する場合に鋳
型材として使用され、その使用法は次の通りであ
る。ワツクスで作製した原型を、歯科用埋没材を
水若しくは専用液で練和して出来たスラリー中に
埋没させ、凝固後に電気炉中で700〜900℃にまで
昇温してワツクスを焼却させ、出来た空洞に溶融
した合金を注入している。
歯科用埋没材は主に結合材と耐火材とから成
り、結合材は埋没材を凝固させると共に耐火材粒
子を結合させて凝固後の成形体の強度と凝固時の
膨張とを発現させるのに寄与しており、耐火材は
加熱時の耐火性を与えると共に熱膨張を発現させ
る働きを有している。凝固膨張と熱膨張は、鋳型
を膨張させることにより鋳造時の合金の収縮を補
正して鋳造体を原型と同形状同寸法にするために
必要である。
歯科用埋没材を結合材の種類によつて分類する
と、石膏を結合材としたもの(以下「石膏系埋没
材」という)とリン酸塩を結合材としたもの(以
下「リン酸塩系埋没材」という)に大別され、耐
火材としては石英やクリストバライトなどのシリ
カ粉末が使用される。
石膏系埋没材は半水石膏が二水石膏になる水和
反応を利用して凝固させるものであり、リン酸塩
系埋没材はマグネシウム、カルシウム、ストロン
チウムや亜鉛などの酸化物が第一リン酸アンモニ
ウムや第一リン酸ナトリウムなどの可溶性リン酸
塩と反応して不溶性のリン酸塩を生成する反応を
利用して凝固させるものである。石膏系埋没材は
練和や埋没の際の操作が容易であり、鋳型として
の通気性も優れており、更に鋳造体への焼き付き
が無いなど、リン酸塩系埋没材に比較して非常に
使い易いため金合金、銀合金および金銀パラジウ
ム合金などの鋳造に広く使用されている。
一方、リン酸塩系埋没材はニツケル・クロム合
金の様に高い温度で鋳造した場合にも良好な鋳造
体表面を維持出来るので、1300℃以上の温度で鋳
造する様な場合に多く使用されているが、練和時
の条件が鋳造体の適合度や表面あらさに大きく影
響することや鋳造体に埋没材が焼き付くことから
鋳造後の処理に手間が掛かるなど、操作性の点で
石膏系埋没材より劣つている。
本発明は練和、埋没若しくは鋳造後の処理が容
易で、しかも高温時の強度と耐火性とを増し、更
に鋳造体の表面状態を改善する目的で歯科用埋没
材と組合わせて使用する練和液の開発を目途とし
て研究を重ねた結果、完成したものである。
以下、本発明に係る歯科用埋没材の練和液につ
いて詳細に説明する。
本発明において着目した点は石膏系埋没材の操
作性の具えた歯科用埋没材練和物を作るための歯
科用埋没材の練和液の開発である。
石膏系埋没材を専用の練和液で練和することに
より、この目的を達成すべく検討を重ねた結果、
石膏系埋没材をリン酸アルミニウム0.6〜6重量
%、塩化ナトリウム1〜3重量%および界面活性
剤10〜100ppmを含み、PHが1.6以上である水溶液
で練和するのが有効であることを見い出した。な
お埋没材粉末に対し加えるべき練和液の混液比は
1:0.2〜0.4が適当である。
本発明に用いられるリン酸アルミニウムには第
一リン酸アルミニウム、第二リン酸アルミニウム
若しくは第三リン酸アルミニウムが効果がある
が、第二リン酸アルミニウムと第三リン酸アルミ
ニウムは溶解度が低いためにPHを下げる必要があ
る。しかし、この目的には殆んどの無機酸を使用
することが出来るが硫酸は不溶性の生成物を生じ
るので適当でない。
次に塩化ナトリウムは他の塩化物、つまり塩化
カリウム、塩化カルシウム、塩化マグネシウムな
どで置き換えることも可能であるが、最も効果の
大きいのは塩化ナトリウムである。
更に界面活性剤については非イオン系と陰イオ
ン系のものが適している。
特許請求の範囲において限定を加えている理由
は次に示す通りである。
リン酸アルミニウムは鋳型の加熱時の強度を出
すと共に鋳造体の表面を改善するが0.6%に満た
ないと鋳造体表面の改善効果が充分でなく、6%
を超えると凝固時間の遅延や鋳造体への埋没材の
焼き付きの問題が出て来るので0.6〜6%とした。
塩化ナトリウムも鋳造体表面を改善するのに役立
つが、1%に満たないと効果が充分でなく、3%
を超えると鋳型を加熱する際に刺激性の塩素ガス
を生じるので1〜3%とした。
界面活性剤もまた鋳造体表面を改善するのに効
果があるが、10ppmに満たないと効果が無く、
100ppmを超えると埋没材の凝固時間を遅延させ、
反えつて鋳造体の面粗れの原因になるので10〜
100ppmとした。
一般には界面活性剤と組合わせて、極く微量の
消泡剤を用いる場合があるが、それは当然本発明
中に包含されるものである。PHは1.6に満たない
とリン酸アルミニウムの溶解が困難なため1.6以
上とした。
以下に実施例を挙げて詳細に説明する。尚茲で
いう%は全て重量%である。
本発明練和液1
第三リン酸アルミニウム6g(0.6%)と塩化
ナトリウム30g(3%)とを水中に投じ、更にリ
ン酸を加えて完全に溶解した後、水を加えて1000
gとした。これにスルフオン系界面活性剤(陰イ
オン系)50ppmを滴下した。PHメーターでPHを測
定した処、3.0であつた。
本発明練和液2
第一リン酸アルミニウム60g(6%)と塩化ナ
トリウム10g(1%)とを水930g(93%)に溶
解し、更に弗素系界面活性剤(陰イオン系)
50pmを滴下した、PHメーターでPHを測定した処、
1.6であつた。
本発明練和液3
第二リン酸アルミニウム33g(3.3%)と塩化
ナトリウム20g(2%)とを水に投じ、更にリン
酸を加えて溶解した後、弗素系界面活性剤(非イ
オン系)50ppmを滴下し、水を加えて1000gとし
た。PHメーターを用いてPHを側定した処、2.4で
あつた。
比較用練和液1
練和液として水だけを用いた。
比較用練和液2
第一リン酸アルミニウム33g(3.3%)を水967
g(96.7%)に溶解し、更に弗素系界面活性剤
(非イオン系)50ppmを滴下した。
比較用練和液3
第一リン酸アルミニウム33g(3.3%)と塩化
ナトリウム20g(2%)とを水947g(94.7%)
に溶解した。
実施例 1
歯科用硬石膏〔JIS T6605、歯科用硬質せつこ
う〕300g(30%)、鋳物用硅砂〔JIS G5901、鋳
型用けい砂〕700g(70%)をミキサーで均一に
混合した。この様にして調製したものを本発明練
和液1を用いて練和し、「JIS T6601歯科鋳造用
埋没材」の方法により試験した処、破砕抗力は51
Kg/cm2であつた。また700℃に加熱した後の破砕
抗力は60Kg/cm2であつた。次に表面が平滑なワツ
クス板を埋没し、700℃にまで加熱してワツクス
を焼却した後、1400℃の溶融歯科用ニツケル・ク
ロム合金を用いて鋳造し、冷却してから鋳造体を
取り出した処、表面は美麗で表面あらさは中心線
平均あらさで2.1μmであつた。
実施例 2〜8
市販の歯科用埋没材のうち石膏系埋没材につい
て、インレー用、クラウン用、鋳造床用を本発明
練和液1〜3の練和液を使用して実施例1と同様
にして試験を行なつた。結果を第1表に示した。
The present invention relates to a mixing liquid for dental gypsum-based investment materials. Dental investment materials are in powder form and are used after being mixed with water or a special mixing liquid. A dental investment material is used as a mold material when manufacturing a dental prosthesis by precision casting, and its usage is as follows. A prototype made of wax is immersed in a slurry made by kneading dental investment material with water or a special liquid, and after solidification, the wax is incinerated by increasing the temperature to 700 to 900 degrees Celsius in an electric furnace. Molten alloy is injected into the resulting cavity. Dental investment materials mainly consist of a binding material and a refractory material, and the binding material solidifies the investment material and binds the refractory material particles to give the molded product strength after solidification and expansion during solidification. The refractory material has the function of providing fire resistance during heating and causing thermal expansion. Solidification expansion and thermal expansion are necessary to compensate for the shrinkage of the alloy during casting by expanding the mold, and to make the cast body the same shape and size as the original. Dental investment materials can be classified according to the type of binding material: those that use gypsum as a binding material (hereinafter referred to as "gypsum-based investment materials") and those that use phosphate as a binding material (hereinafter referred to as "phosphate-based investment materials"). Silica powder such as quartz and cristobalite is used as the refractory material. Gypsum-based investment materials solidify using a hydration reaction in which gypsum hemihydrate becomes gypsum dihydrate, while phosphate-based investment materials solidify oxides such as magnesium, calcium, strontium, and zinc into primary phosphate. It is solidified using a reaction in which it reacts with soluble phosphates such as ammonium and monosodium phosphate to produce insoluble phosphates. Compared to phosphate-based investment materials, gypsum-based investment materials are easy to operate during mixing and burial, have excellent air permeability as molds, and do not seize on cast objects. Because it is easy to use, it is widely used for casting gold alloys, silver alloys, and gold-silver-palladium alloys. On the other hand, phosphate-based investment materials, such as nickel-chromium alloys, can maintain a good cast surface even when cast at high temperatures, so they are often used when casting at temperatures of 1300°C or higher. However, from the viewpoint of operability, gypsum-based investment is difficult, as the conditions during mixing greatly affect the suitability and surface roughness of the cast object, and the investment material sticks to the cast object, making post-casting processing time-consuming. It is inferior to wood. The present invention is a compound that can be used in combination with dental investment materials for the purpose of being easy to process after mixing, embedding, or casting, increasing the strength and fire resistance at high temperatures, and further improving the surface condition of the cast body. This was completed as a result of repeated research aimed at developing a Japanese liquid. Hereinafter, the mixing liquid for the dental investment material according to the present invention will be explained in detail. The focus of the present invention is on the development of a dental investment material mixture for producing a dental investment material mixture that has the operability of a gypsum-based investment material. As a result of repeated studies to achieve this objective by mixing the gypsum investment material with a special mixing solution, we found that
It was discovered that it is effective to knead a gypsum-based investment material with an aqueous solution containing 0.6 to 6% by weight of aluminum phosphate, 1 to 3% by weight of sodium chloride, and 10 to 100 ppm of a surfactant, and having a pH of 1.6 or higher. Ta. The mixing ratio of the kneading liquid to the investment material powder is preferably 1:0.2 to 0.4. As the aluminum phosphate used in the present invention, primary aluminum phosphate, secondary aluminum phosphate, or tertiary aluminum phosphate is effective, but dibasic aluminum phosphate and tertiary aluminum phosphate have low solubility. It is necessary to lower the PH. However, although most inorganic acids can be used for this purpose, sulfuric acid is not suitable since it produces insoluble products. Next, sodium chloride can be replaced with other chlorides, such as potassium chloride, calcium chloride, magnesium chloride, etc., but sodium chloride is the most effective. Furthermore, nonionic and anionic surfactants are suitable. The reason for adding limitations to the scope of the claims is as follows. Aluminum phosphate provides strength when heating the mold and improves the surface of the cast body, but if it is less than 0.6%, the effect of improving the surface of the cast body is not sufficient;
If it exceeds this, problems such as delay in solidification time and sticking of the investment material to the cast body will occur, so it was set at 0.6 to 6%.
Sodium chloride is also useful for improving the surface of castings, but if it is less than 1%, the effect is not sufficient;
If it exceeds 1%, irritating chlorine gas will be generated when heating the mold, so it was set at 1% to 3%. Surfactants are also effective in improving the surface of castings, but they are ineffective at less than 10 ppm;
If it exceeds 100ppm, it will delay the solidification time of the investment material.
10~ to avoid warping and causing surface roughness of the cast body.
It was set to 100ppm. Generally, a very small amount of an antifoaming agent may be used in combination with a surfactant, which is naturally included in the present invention. If the pH is less than 1.6, it is difficult to dissolve aluminum phosphate, so the pH was set to 1.6 or higher. Examples will be described in detail below. All percentages mentioned herein are percentages by weight. Kneading solution 1 of the present invention: 6 g (0.6%) of tertiary aluminum phosphate and 30 g (3%) of sodium chloride are poured into water, and after adding phosphoric acid to completely dissolve, water is added to
g. 50 ppm of sulfonic surfactant (anionic) was added dropwise to this. I measured the pH with a PH meter and it was 3.0. Kneading solution 2 of the present invention 60g (6%) of primary aluminum phosphate and 10g (1%) of sodium chloride are dissolved in 930g (93%) of water, and a fluorine-based surfactant (anionic) is added.
When 50pm was dropped and the PH was measured with a PH meter,
It was 1.6. Kneading solution 3 of the present invention 33 g (3.3%) of di-aluminum phosphate and 20 g (2%) of sodium chloride are poured into water, phosphoric acid is added and dissolved, and a fluorine-based surfactant (nonionic) is added. 50 ppm was added dropwise and water was added to make 1000 g. I determined the pH using a PH meter and found it to be 2.4. Comparative Kneading Solution 1 Only water was used as the kneading solution. Comparative kneading solution 2 33g (3.3%) of primary aluminum phosphate in 967ml of water
g (96.7%), and 50 ppm of a fluorine-based surfactant (nonionic) was added dropwise. Comparative kneading solution 3 33g (3.3%) of primary aluminum phosphate and 20g (2%) of sodium chloride were mixed with 947g (94.7%) of water.
dissolved in Example 1 300 g (30%) of dental anhydrite [JIS T6605, hard plaster for dentistry] and 700 g (70%) of silica sand for foundry use [JIS G5901, silica sand for molding] were mixed uniformly with a mixer. The product prepared in this way was kneaded using the mixing liquid 1 of the present invention and tested according to the method of "JIS T6601 Dental casting investment materials", and the crushing resistance was 51.
It was Kg/ cm2 . Moreover, the crushing force after heating to 700°C was 60Kg/cm 2 . Next, a wax plate with a smooth surface was buried, heated to 700°C to incinerate the wax, and then cast using molten dental nickel-chromium alloy at 1400°C. After cooling, the cast body was removed. The surface was beautiful and the average center line roughness was 2.1 μm. Examples 2 to 8 Among commercially available dental investment materials, gypsum-based investment materials for inlays, crowns, and cast beds were prepared in the same manner as in Example 1 using the mixing solutions 1 to 3 of the present invention. The test was carried out as follows. The results are shown in Table 1.
【表】
なお本発明練和液3を用い実施例8において、
埋没材を練和し凝固させたものを鋳型として歯科
用ニツケル・クロム合金を鋳造した場合の鋳造物
の表面のあらさを測定した結果を第1図に示す。
比較例 1〜4
実施例と同一の方法により比較用練和液を用い
て試験を行ないその結果を第2表に示した。
比較例2における比較用練和液1を用いた場
合、比較例3における比較用練和液2を用いた場
合における夫々の鋳造物の表面あらさを測定した
結果を第2図および第3図に示した。[Table] In Example 8 using the kneading solution 3 of the present invention,
Figure 1 shows the results of measuring the surface roughness of a dental nickel-chromium alloy cast using a kneaded and solidified investment material as a mold. Comparative Examples 1 to 4 Tests were conducted using comparative kneading solutions in the same manner as in the examples, and the results are shown in Table 2. Figures 2 and 3 show the results of measuring the surface roughness of each casting when Comparative Mixing Solution 1 in Comparative Example 2 and Comparative Mixing Solution 2 in Comparative Example 3 were used. Indicated.
【表】【table】
【表】
以上述べた如く、石膏系埋没材を本発明品で練
和することにより、ニツケル・クロム合金の鋳造
が可能になつた。このことはニツケル・クロム合
金による補綴物の製作を容易にし、歯科医療を飛
躍的に向上させるものである。[Table] As described above, by mixing the gypsum investment material with the product of the present invention, it became possible to cast a nickel-chromium alloy. This makes it easier to manufacture prosthetics made of nickel-chromium alloy and dramatically improves dental care.
第1図は実施例8の練和液を用いて埋没材を凝
固させたものを用い歯科用ニツケル・クロム合金
を鋳造した場合の該鋳造物の表面あらさを測定し
た図であり、第2図は比較例2の場合であり、第
3図は比較例3の場合を示す。
Figure 1 is a diagram showing the measurement of the surface roughness of a dental nickel-chromium alloy cast using the investment material solidified using the mixing solution of Example 8, and Figure 2. shows the case of Comparative Example 2, and FIG. 3 shows the case of Comparative Example 3.
Claims (1)
0.6〜6%、塩化ナトリウム1〜3%および界面
活性剤10〜100ppmを含み、PHが1.6以上である歯
科用石膏系埋没材練和液。1 aluminum phosphate as weight percent
A dental gypsum-based investment material mixing liquid containing 0.6 to 6% sodium chloride, 1 to 3% sodium chloride, and 10 to 100 ppm of a surfactant, and having a pH of 1.6 or more.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58053800A JPS59181204A (en) | 1983-03-31 | 1983-03-31 | Kneading liquid of dental investment material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58053800A JPS59181204A (en) | 1983-03-31 | 1983-03-31 | Kneading liquid of dental investment material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59181204A JPS59181204A (en) | 1984-10-15 |
| JPS632521B2 true JPS632521B2 (en) | 1988-01-19 |
Family
ID=12952887
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58053800A Granted JPS59181204A (en) | 1983-03-31 | 1983-03-31 | Kneading liquid of dental investment material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59181204A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH09195738A (en) * | 1996-01-18 | 1997-07-29 | Komatsu Ltd | ENGINE VALVE MECHANISM CONTROL DEVICE AND ITS CONTROL METHOD |
| JP4294037B2 (en) * | 2006-06-13 | 2009-07-08 | 大成歯科工業株式会社 | Phosphate-based dental investment |
-
1983
- 1983-03-31 JP JP58053800A patent/JPS59181204A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59181204A (en) | 1984-10-15 |
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