JP2872485B2 - Dental wax composition - Google Patents

Dental wax composition

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Publication number
JP2872485B2
JP2872485B2 JP15415992A JP15415992A JP2872485B2 JP 2872485 B2 JP2872485 B2 JP 2872485B2 JP 15415992 A JP15415992 A JP 15415992A JP 15415992 A JP15415992 A JP 15415992A JP 2872485 B2 JP2872485 B2 JP 2872485B2
Authority
JP
Japan
Prior art keywords
wax
weight
dental
softening point
resin
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 - Fee Related
Application number
JP15415992A
Other languages
Japanese (ja)
Other versions
JPH05320021A (en
Inventor
春一 二見
暢之 服部
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.)
JII SHII KK
Original Assignee
JII SHII KK
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Filing date
Publication date
Application filed by JII SHII KK filed Critical JII SHII KK
Priority to JP15415992A priority Critical patent/JP2872485B2/en
Publication of JPH05320021A publication Critical patent/JPH05320021A/en
Application granted granted Critical
Publication of JP2872485B2 publication Critical patent/JP2872485B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Dental Preparations (AREA)
  • Dental Prosthetics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は歯科用精密鋳造用蝋型の
作成に用いられる歯科用ワックス組成物に関するもので
ある。特に本発明の歯科用ワックス組成物は、歯質欠損
インレー或いはクラウン等を鋳造するのに最大限正確に
再現した蝋型を造るためのものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a dental wax composition used for making a wax mold for precision dental casting. In particular, the dental wax composition of the present invention is for producing a wax mold that reproduces as accurately as possible for casting tooth-deficient inlays or crowns.

【0002】[0002]

【従来の技術及び課題】従来、歯科用精密鋳造に於ける
蝋型材料としては動植物系、鉱物系、石油系及び合成系
の各種ワックス類、天然樹脂及び石油樹脂が使用されて
来た。即ち、パラフィンワックスを主成分として、蜜
蝋,マイクロクリスタリンワックスにより柔軟性、粘着
性を与え、ダンマーやロジン、石油樹脂を加えて硬さや
強度を改善し、粘り強さを与え、また高融点のカルナバ
ワックスを加えてワックスの表面に光沢を与えて歯科用
ワックス、特に歯科鋳造用ワックスが造られて来てい
る。蝋型はどのように作られるにせよ、それは歯質欠損
を正確に再現しなければならない。蝋型は金属を鋳造す
る鋳型の輪郭となるものであるから、他の操作を如何に
注意深く行っても鋳造体の方が蝋型より正確になるよう
なことはあり得ない。従って蝋型を窩洞に良く適合さ
せ、正しく彫刻し、変形を出来るだけ少なくすることが
必要である。
2. Description of the Related Art Conventionally, various waxes, natural resins and petroleum resins of animal and plant type, mineral type, petroleum type and synthetic type have been used as wax type materials in dental precision casting. That is, paraffin wax is used as a main component, and beeswax and microcrystalline wax are used to impart flexibility and tackiness. Dummar, rosin and petroleum resin are added to improve hardness and strength, to give toughness, and to provide a high melting point carnauba wax. In addition, dental waxes, especially dental casting waxes, have been produced by imparting gloss to the surface of the wax. No matter how the wax mold is made, it must accurately reproduce the tooth defect. Since the wax mold is the contour of the mold from which the metal is cast, no matter how carefully the other operations are performed, the casting can never be more accurate than the wax mold. Therefore, it is necessary that the wax mold be well fitted to the cavity, properly sculpted and deformed as little as possible.

【0003】蝋型は窩洞から取り外された後、石膏を含
む埋没材の中に埋没される。そして埋没材が硬化して
後、約700℃迄加熱して蝋を完全に焼却させるのであ
る。このようなワックス組成物は、ダンマー,ロジン等
の天然樹脂を用いているため、耐久性が無く、ワックス
との相溶性の低下が認められ、歯科鋳造用ワックスとし
て不利であった。更に、密蝋、マイクロクリスタリンワ
ックスを加えることにより柔軟性を与え、使い易くはな
るが、ワックス形成、彫刻時にベタ付いてワックスが、
付着し易くなり、反って使い難くなる。また、密蝋やカ
ルナバワックス等動植物系ワックスは高価であるのが欠
点である。更にワックスの収縮が大きいのが現状であ
る。
[0003] After the wax mold is removed from the cavity, it is immersed in an investment material containing gypsum. After the investment material has hardened, it is heated to about 700 ° C. to completely incinerate the wax. Since such a wax composition uses a natural resin such as a dammer and rosin, it has no durability and a decrease in compatibility with the wax, which is disadvantageous as a wax for dental casting. Furthermore, beeswax and microcrystalline wax are added to give flexibility and ease of use, but wax formation, engraving during engraving,
It becomes easy to adhere and becomes difficult to use. Also, animal and plant waxes such as beeswax and carnauba wax are expensive. Further, at present, the shrinkage of the wax is large.

【0004】[0004]

【課題を解決するための手段】本発明は、従来の歯科鋳
造用ワックスに於ける上記の欠点を改良することを目的
とするものである。本発明は天然樹脂に代わり、ワック
スとの相溶性に優れた合成樹脂である、炭化水素樹脂と
エチレン・酢酸ビニル共重合樹脂とを組合わせて用いる
ことによって蝋型の作成が容易で、且つ極めて安定な歯
科鋳造用ワックスを得ることが出来た。従来、ロジン系
樹脂、密蝋やマイクロクリスタリンワックスを用いたこ
とにより、ワックス彫刻時のベタツキの原因となってい
たが、本発明では、これ等ロジン系樹脂、密蝋及びマイ
クロクリスタリンワックスを除去し、エチレン・酢酸ビ
ニル共重合樹脂を好ましくは1〜5重量%配合すること
によって適性な柔軟性をワックスに与えて改質すること
が出来たのである。
SUMMARY OF THE INVENTION An object of the present invention is to remedy the above-mentioned disadvantages of the conventional dental casting wax. The present invention is a synthetic resin having excellent compatibility with wax instead of a natural resin.By using a hydrocarbon resin in combination with an ethylene-vinyl acetate copolymer resin, it is easy to prepare a wax mold, and extremely. A stable dental casting wax was obtained. Conventionally, the use of rosin-based resin, beeswax or microcrystalline wax has caused stickiness during wax engraving, but in the present invention, these rosin-based resins, beeswax and microcrystalline wax are removed. By blending the ethylene / vinyl acetate copolymer resin preferably in an amount of 1 to 5% by weight, the wax was given appropriate flexibility and could be modified.

【0005】更には、パラフィンワックスと合成ワック
スを組み合わせ、炭化水素樹脂の有効な配合量10〜4
0重量%とエチレン・酢酸ビニル共重合樹脂1〜5重量
%を配合することによって、比較的収縮の小さい、歯科
鋳造用ワックスを作成することに至った。即ち、本発明
は軟化点が80〜140℃の炭化水素樹脂10〜40重
量%、エチレン・酢酸ビニル共重合樹脂1〜5重量%、
パラフィンワックス40〜80重量%、合成ワックス1
〜15重量%含有せしめることを特徴とする好ましい歯
科用ワックス組成物を作製することが出来たのである。
このように本発明による歯科用ワックス組成物の特徴は
合成樹脂である炭化水素樹脂とエチレン・酢酸ビニル共
重合樹脂とを組合わせ、パラフィンワックスと高融点を
示す合成ワックスとを特定の割合に配合したワックスを
用いた点に在る。
Further, a paraffin wax and a synthetic wax are combined to form an effective blending amount of a hydrocarbon resin of 10 to 4 times.
By blending 0% by weight and 1 to 5% by weight of an ethylene / vinyl acetate copolymer resin, a wax for dental casting having relatively small shrinkage was obtained. That is, the present invention provides a softening point of a hydrocarbon resin having a softening point of 80 to 140 ° C. by 10 to 40% by weight, an ethylene / vinyl acetate copolymer resin by 1 to 5% by weight,
40-80% by weight of paraffin wax, synthetic wax 1
Thus, a preferred dental wax composition characterized by containing 含有 15% by weight was able to be produced.
As described above, the characteristic of the dental wax composition according to the present invention is that a hydrocarbon resin as a synthetic resin is combined with an ethylene / vinyl acetate copolymer resin, and a paraffin wax and a synthetic wax having a high melting point are blended in a specific ratio. The point is that the used wax is used.

【0006】本発明では、従来歯科用ワックスに用いら
れて来た天然樹脂、動植物系ワックスは使用しない。こ
こで歯科用ワックスの成分を更に具体的に例示すると、
炭化水素樹脂は軟化点(環球法)80〜140℃の脂環
族飽和炭化水素樹脂、脂肪族炭化水素樹脂、脂肪族/芳
香族共重合樹脂から成り、軟化点(環球法)80〜12
0℃以下のエチレン・酢酸ビニル共重合樹脂と組合わせ
ることが歯科用ワックスの柔軟性、強度、溶解容易性か
ら考えて好ましい。パラフィンワックスは融点が120
〜150°Fのものが使用上適当であり、また合成ワッ
クスはフィッシャートロプシュワックス、硬化ヒマシ
油、ヒドロキシステアリン酸及び低分子ポリエチレンが
カルナバワックスに代わり用いられる。
In the present invention, natural resins and animal and plant waxes conventionally used for dental waxes are not used. Here, when the components of the dental wax are more specifically exemplified,
The hydrocarbon resin is composed of an alicyclic saturated hydrocarbon resin having a softening point (ring and ball method) of 80 to 140 ° C., an aliphatic hydrocarbon resin, and an aliphatic / aromatic copolymer resin.
It is preferable to combine with an ethylene / vinyl acetate copolymer resin having a temperature of 0 ° C. or lower in view of the flexibility, strength, and ease of dissolution of the dental wax. Paraffin wax has a melting point of 120
A wax having a temperature of ~ 150 ° F is suitable for use, and Fischer-Tropsch wax, hydrogenated castor oil, hydroxystearic acid and low molecular weight polyethylene are used instead of carnauba wax as synthetic waxes.

【0007】炭化水素樹脂は、ワックスとの相溶性が良
く、耐光・耐熱性であり、安定な物質である。軟化点が
80℃以下であると歯科用ワックスとして変形の恐れが
あり、また140℃以上であると軟化・溶解操作が難し
くなるので適当ではない。この樹脂の配合割合が10重
量%未満のものは硬さ、強度が充分発揮されず、40重
量%を超えるとワックスとしての特性が失われ、彫刻性
が無くなって蝋型の作成が困難になるので適当ではな
い。従って本発明の歯科用ワックス組成物に用いる軟化
点が80〜140℃の炭化水素樹脂は10〜40重量%
が好適である。
[0007] Hydrocarbon resins have good compatibility with wax, are light and heat resistant, and are stable substances. If the softening point is less than 80 ° C., there is a risk of deformation as a dental wax, and if it is more than 140 ° C., the softening / dissolving operation becomes difficult, which is not appropriate. If the content of this resin is less than 10% by weight, the hardness and strength are not sufficiently exhibited, and if it exceeds 40% by weight, the properties as a wax are lost, the engraving property is lost, and it becomes difficult to prepare a wax mold. Not so. Therefore, the hydrocarbon resin having a softening point of 80 to 140 ° C. used in the dental wax composition of the present invention is 10 to 40% by weight.
Is preferred.

【0008】エチレン・酢酸ビニル共重合樹脂は軟化点
(環球法)が80℃から120℃の範囲のものがワック
スへの溶解性が良く、大きな変形の恐れが無いので適当
であり、エチレン・酢酸ビニル共重合樹脂の含有量が1
重量%未満では強靱性が発現されず、5重量%超では変
形の傾向が大きく好ましくない。従って本発明の歯科用
ワックス組成物に用いられる軟化点(環球法)が80〜
120℃のエチレン・酢酸ビニル共重合樹脂は1〜5重
量%が好適である。パラフィンワックスは融点が120
〜150°Fのものが用いられる。パラフィンワックス
が40重量%未満のものは軟化溶解がスムーズでなく、
ワックスの感覚が無くなり彫刻性が悪くなり蝋型の作成
が困難となる。また80重量%を超えるとパラフィンワ
ックスの脆い性質が強くなり、彫刻性が極度に低下する
ので不適当である。従ってパラフィンワックスの配合は
40〜80重量%が好適である。
Ethylene-vinyl acetate copolymer resins having a softening point (ring and ball method) in the range of 80 ° C. to 120 ° C. are suitable because they have good solubility in wax and do not have a large risk of deformation. Content of vinyl copolymer resin is 1
If it is less than 5% by weight, the toughness is not exhibited, and if it exceeds 5% by weight, the tendency of deformation is large, which is not preferable. Therefore, the softening point (ring and ball method) used for the dental wax composition of the present invention is 80 to 80.
The amount of the ethylene / vinyl acetate copolymer resin at 120 ° C. is preferably 1 to 5% by weight. Paraffin wax has a melting point of 120
~ 150 ° F is used. If the paraffin wax is less than 40% by weight, the softening and dissolving is not smooth,
The feeling of the wax is lost, the sculpability deteriorates, and it becomes difficult to prepare a wax mold. On the other hand, if it exceeds 80% by weight, the brittle nature of paraffin wax becomes strong, and the engraving property is extremely lowered, which is not suitable. Therefore, the content of paraffin wax is preferably 40 to 80% by weight.

【0009】合成ワックスは軟化点(環球法)が90〜
120℃のものがワックスに硬さを与え、溶解操作が適
度である。合成ワックスは1重量%未満では硬さの効果
が認められない。また、15重量%超ではワックスの硬
化が速く操作余裕時間が極度に短くなるので適当ではな
い。従って本発明に用いられる合成ワックスは1〜15
重量%が好適である。以上、本発明に於ける組成に就い
て詳述して来たが、実施例を示してその効果を説明する
が、本発明はこれに限定されるものではない。
The synthetic wax has a softening point (ring and ball method) of 90 to 90.
Those at 120 ° C. impart hardness to the wax, and the melting operation is moderate. If the synthetic wax is less than 1% by weight, the effect of hardness is not recognized. On the other hand, if it exceeds 15% by weight, the wax is hardened rapidly and the operation allowance time becomes extremely short, so that it is not appropriate. Therefore, the synthetic wax used in the present invention is 1 to 15
% By weight is preferred. The composition of the present invention has been described in detail above. The effects will be described with reference to examples, but the present invention is not limited to these examples.

【0010】[0010]

【実施例】実施例1 (重量%) 脂環族炭化水素樹脂(軟化点135℃) 20 脂肪族/芳香族炭化水素樹脂(軟化点95℃) 10 エチレン・酢酸ビニル共重合樹脂(軟化点100℃) 4 130°Fパラフィンワックス 64 低分子ポリエチレン(商品名サンワックス131−P・荒川化学社製) 1 フィッシャートロップシュワックス(凝固点95℃) 1EXAMPLES Example 1 (% by weight) Alicyclic hydrocarbon resin (softening point 135 ° C) 20 Aliphatic / aromatic hydrocarbon resin (softening point 95 ° C) 10 Ethylene / vinyl acetate copolymer resin (softening point 100 ° C) 4 130 ° F paraffin wax 64 Low molecular weight polyethylene (trade name: Sunwax 131-P, manufactured by Arakawa Chemical Co., Ltd.) 1 Fischer Tropsch wax (coagulation point 95 ° C) 1

【0011】上記6成分を計量して電気溶解釜に投入
し、130℃に設定した温度で20分間加熱、撹拌して
完全に溶解した。直ちに濾過して、棒状、板状或いは缶
に入れて保管、試料とした。試験の結果は表1の通りで
あり、特に針入度が比較例に比べ小さい値を示して硬い
性質を表わし、また熱膨張率は約20%減少した。ワッ
クスの削り感はベタツキが無く良好であった。
The above-mentioned six components were weighed and put into an electric melting pot, heated and stirred at a temperature set at 130 ° C. for 20 minutes, and completely dissolved. Immediately after filtration, the sample was stored in a rod shape, a plate shape, or a can to obtain a sample. The test results are as shown in Table 1. In particular, the penetration was smaller than that of the comparative example, indicating a hard property, and the coefficient of thermal expansion was reduced by about 20%. The abrasion feeling of the wax was good without stickiness.

【0012】実施例2 (重量%) 脂環族炭化水素樹脂(軟化点90℃) 8 脂肪族炭化水素樹脂(軟化点100℃) 7 エチレン・酢酸ビニル共重合樹脂(軟化点85℃) 2 140°Fパラフィンワックス 52 125°Fパラフィンワックス 26 フィッシャートロップシュワックス(凝固点95℃) 5Example 2 (% by weight) Alicyclic hydrocarbon resin (softening point 90 ° C.) 8 Aliphatic hydrocarbon resin (softening point 100 ° C.) 7 Ethylene / vinyl acetate copolymer resin (softening point 85 ° C.) 2 140 ° F paraffin wax 52 125 ° F paraffin wax 26 Fischer-Tropsch wax (freezing point 95 ° C) 5

【0013】上記6成分を計量して電気溶解釜に投入
し、110℃に設定した温度で20分間加熱、撹拌して
完全に溶解した。直ちに濾過して、棒状、板状或いは缶
に入れて保管し試料とした。試験の結果は表1の通りで
あり、比較例に比べ針入度が小さい値を示して硬い性質
を表わし、また熱膨張率は約25%減少した。ワックス
の削り感はベタツキが無く良好であった。
The above-mentioned six components were weighed and put into an electric melting vessel, heated and stirred at a temperature set at 110 ° C. for 20 minutes, and completely dissolved. The sample was immediately filtered, stored in a rod shape, a plate shape, or a can to obtain a sample. The results of the test are as shown in Table 1. The penetration was smaller than that of the comparative example, indicating a hard property, and the coefficient of thermal expansion was reduced by about 25%. The abrasion feeling of the wax was good without stickiness.

【0014】実施例3 (重量%) 脂環族炭化水素樹脂(軟化点115℃) 38 エチレン・酢酸ビニル共重合樹脂(軟化点120℃) 3 145°Fパラフィンワックス 15 130°Fパラフィンワックス 30 硬化ヒマシ油 8 ヒドロキシステアリン酸 6Example 3 (wt%) Alicyclic hydrocarbon resin (softening point 115 ° C) 38 Ethylene / vinyl acetate copolymer resin (softening point 120 ° C) 3 145 ° F paraffin wax 15 130 ° F paraffin wax 30 Curing Castor oil 8 Hydroxystearic acid 6

【0015】上記6成分を計量して電気溶解釜に投入
し、120℃に設定した温度で20分間加熱、撹拌して
完全に溶解した。直ちに濾過して、棒状、板状或いは缶
に入れて保管し試料とした。試験の結果は表1の通りで
あり、比較例に比べ針入度が小さく硬い性質を示し、ま
た熱膨張率は約40%減少した。ワックスの削り感はベ
タツキが無く良好であった。
The above-mentioned six components were weighed and put into an electric melting pot, heated and stirred at a temperature set at 120 ° C. for 20 minutes, and completely dissolved. The sample was immediately filtered, stored in a rod shape, a plate shape, or a can to obtain a sample. The results of the test are as shown in Table 1, showing that the penetration was small and hard compared to the comparative example, and the coefficient of thermal expansion was reduced by about 40%. The abrasion feeling of the wax was good without stickiness.

【0016】比較例1 (重量%) ダンマー 13 130°Fパラフィンワックス 45 140°Fパラフィンワックス 30 カルナバワックス 10 密蝋 2Comparative Example 1 (% by weight) Dammer 13 130 ° F. paraffin wax 45 140 ° F. paraffin wax 30 carnauba wax 10 beeswax 2

【0017】上記5成分を計量して電気溶解釜に投入
し、110℃に設定した温度で20分間加熱、撹拌し完
全に溶解した。直ちに濾過して、棒状、板状或いは缶に
入れて保管し試料とした。試験の結果は表1に示した通
りである。凝固点は57.4℃を示し、針入度は0.8
0(mm)で通常の歯科用ワックスの範囲内であり、熱膨
張率は0.45%であった。このワックスは彫刻時ベタ
ツキ感は有るが、蝋型の形成は可能であった。6ヶ月室
温放置後、加熱溶解し、盛り上げ成形する場合、完全溶
解せず、一部残渣が認められた。
The above five components were weighed and put into an electric melting vessel, and heated and stirred at a temperature set at 110 ° C. for 20 minutes to completely dissolve. The sample was immediately filtered, stored in a rod shape, a plate shape, or a can to obtain a sample. The test results are as shown in Table 1. The freezing point is 57.4 ° C. and the penetration is 0.8.
It was 0 (mm), which was within the range of ordinary dental wax, and the coefficient of thermal expansion was 0.45%. This wax had a sticky feeling during engraving, but could form a wax pattern. When left at room temperature for 6 months and then heated and melted to form a swell, it was not completely dissolved and some residues were observed.

【0018】[0018]

【表1】 [Table 1]

【0019】熱膨張率 :JIS T−6503の方法
による。 針入度 :直径10mm、高さ6mmに成形した試料を恒
温恒湿中(23±1℃,50±1%)において、荷重3
00gを直径1.0mmのビッカー針を用いて5秒間加
え、その深さを測定した。数値が小さい程硬さは大き
い。 彫刻性 :ワックスインスツルメントを用いてワック
スの削り具合を調べた。 加熱溶解性:試料1gを110℃中に5分間放置し、溶
解残渣の有無を調べた。
Thermal expansion coefficient: According to the method of JIS T-6503. Penetration: A sample molded to a diameter of 10 mm and a height of 6 mm was subjected to a load of 3 under constant temperature and humidity (23 ± 1 ° C., 50 ± 1%).
00g was added for 5 seconds using a 1.0 mm diameter Vickers needle, and the depth was measured. The smaller the value, the greater the hardness. Engravability: The degree of shaving of the wax was examined using a wax instrument. Heat solubility: 1 g of the sample was left at 110 ° C. for 5 minutes, and the presence or absence of a dissolved residue was examined.

【0020】[0020]

【発明の効果】表1の試験結果より明らかな様に本発明
に於ける歯科用ワックス組成物は特に鋳造用のインレー
ワックスとして、加熱溶解時、残渣が全く無く極めて安
定であり、またベタツキが無く彫刻性もスムーズに出
来、膨張、収縮が小さく、且つ針入度が小さく硬さが大
きいため、変形の少ない歯科用ワックス組成物を初めて
造ることに成功した。
As is clear from the test results in Table 1, the dental wax composition of the present invention is particularly stable as an inlay wax for casting without any residue when melted by heating, and has a stickiness. Because of this, the engravability was smooth, the expansion and shrinkage were small, the penetration was small, and the hardness was large. Therefore, the dental wax composition with little deformation was successfully produced for the first time.

───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.6,DB名) A61K 6/00 A61C 13/20 ──────────────────────────────────────────────────続 き Continued on front page (58) Field surveyed (Int. Cl. 6 , DB name) A61K 6/00 A61C 13/20

Claims (4)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 パラフィンワックス40〜80重量%と
合成ワックス1〜15重量%に炭化水素樹脂10〜40
重量%とエチレン・酢酸ビニル共重合樹脂1〜5重量%
を組合わせて成ることを特徴とする歯科用ワックス組成
物。
1. A hydrocarbon resin containing 40 to 80% by weight of paraffin wax and 1 to 15% by weight of synthetic wax.
% By weight and 1 to 5% by weight of ethylene / vinyl acetate copolymer resin
A dental wax composition comprising a combination of:
【請求項2】 合成ワックスがフィッシャートロプシュ
ワツクス,硬化ヒマシ油,ヒドロキシステアリン酸及び
低分子ポリエチレンの群から選ばれた1種または2種以
上を用いることを特徴とする請求項1に記載の歯科用ワ
ックス組成物。
2. The dental product according to claim 1, wherein the synthetic wax is at least one selected from the group consisting of Fischer-Tropschwax, hydrogenated castor oil, hydroxystearic acid and low molecular weight polyethylene. Wax composition.
【請求項3】 炭化水素樹脂が軟化点80〜140℃で
あることを特徴とする請求項1若しくは2に記載の歯科
用ワックス組成物。
3. The dental wax composition according to claim 1, wherein the hydrocarbon resin has a softening point of 80 to 140 ° C.
【請求項4】 エチレン・酢酸ビニル共重合樹脂が軟化
点80〜120℃であることを特徴とする請求項1ない
し3中のいずれか1項に記載の歯科用ワックス組成物。
4. The dental wax composition according to claim 1, wherein the ethylene / vinyl acetate copolymer resin has a softening point of 80 to 120 ° C.
JP15415992A 1992-05-22 1992-05-22 Dental wax composition Expired - Fee Related JP2872485B2 (en)

Priority Applications (1)

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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15415992A JP2872485B2 (en) 1992-05-22 1992-05-22 Dental wax composition

Publications (2)

Publication Number Publication Date
JPH05320021A JPH05320021A (en) 1993-12-03
JP2872485B2 true JP2872485B2 (en) 1999-03-17

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Country Link
JP (1) JP2872485B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100408222B1 (en) * 2000-10-30 2003-12-01 주식회사 에벡스 Hot melt adhesive film
WO2007061093A1 (en) * 2005-11-28 2007-05-31 Houei Industry Co., Ltd. Machinable wax composition, machinable wax processed product, and their production methods
JP5170532B2 (en) * 2008-01-11 2013-03-27 株式会社デンタス Wax denture
JP2017036241A (en) * 2015-08-10 2017-02-16 デンケン・ハイデンタル株式会社 Composition for formation of biteplate and production method of plate denture using the same

Also Published As

Publication number Publication date
JPH05320021A (en) 1993-12-03

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