JPS6399859A - Mold - Google Patents
MoldInfo
- Publication number
- JPS6399859A JPS6399859A JP61244094A JP24409486A JPS6399859A JP S6399859 A JPS6399859 A JP S6399859A JP 61244094 A JP61244094 A JP 61244094A JP 24409486 A JP24409486 A JP 24409486A JP S6399859 A JPS6399859 A JP S6399859A
- Authority
- JP
- Japan
- Prior art keywords
- mold
- molding
- present
- boron nitride
- fibrous
- 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.)
- Granted
Links
- 239000000463 material Substances 0.000 claims description 22
- 238000000465 moulding Methods 0.000 claims description 18
- 229910052582 BN Inorganic materials 0.000 claims description 15
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims description 15
- 239000002657 fibrous material Substances 0.000 claims description 10
- 239000000126 substance Substances 0.000 claims description 9
- 239000011521 glass Substances 0.000 description 11
- 239000001506 calcium phosphate Substances 0.000 description 9
- 229910000389 calcium phosphate Inorganic materials 0.000 description 9
- 235000011010 calcium phosphates Nutrition 0.000 description 9
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 9
- 239000000835 fiber Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 230000001771 impaired effect Effects 0.000 description 4
- 210000000332 tooth crown Anatomy 0.000 description 4
- 239000012237 artificial material Substances 0.000 description 3
- 210000000988 bone and bone Anatomy 0.000 description 3
- 239000005548 dental material Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000010425 asbestos Substances 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000003631 expected effect Effects 0.000 description 2
- GVALZJMUIHGIMD-UHFFFAOYSA-H magnesium phosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GVALZJMUIHGIMD-UHFFFAOYSA-H 0.000 description 2
- 239000004137 magnesium phosphate Substances 0.000 description 2
- 229910000157 magnesium phosphate Inorganic materials 0.000 description 2
- 229960002261 magnesium phosphate Drugs 0.000 description 2
- 235000010994 magnesium phosphates Nutrition 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 229910052895 riebeckite Inorganic materials 0.000 description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical group N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 1
- 229910052580 B4C Inorganic materials 0.000 description 1
- 244000089486 Phragmites australis subsp australis Species 0.000 description 1
- 235000014676 Phragmites communis Nutrition 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000012620 biological material Substances 0.000 description 1
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000156 glass melt Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
Landscapes
- Materials For Medical Uses (AREA)
- Dental Prosthetics (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Abstract] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は成形用型、特にリン酸カルシウム系結晶化ガラ
スによる歯科材料、骨、関節等の人工材料を成形する際
に用いられる成形用型に係るものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a mold, particularly a mold used for molding dental materials, bones, joints, and other artificial materials made of calcium phosphate crystallized glass. It is something.
[従来の技術]
近年、歯科材料、骨、関節等に各種の人工材料が提案さ
れ、その一部は実用に供されつつある。[Prior Art] In recent years, various artificial materials have been proposed for dental materials, bones, joints, etc., and some of them are being put into practical use.
これら人工材料のうち、リン酸カルシウム系の材料は、
生体の歯や骨の成分と同じか若しくは近似している為、
生体からの拒絶反応も少なく好ましい材料である利点が
ある。このような材料のうち、リン酸カルシウム系結晶
化ガラスは成形性に優れていること、特に物性が天然歯
に酷似している事等の理由から歯科材料としての応用が
期待されている。Among these artificial materials, calcium phosphate materials are
Because it is the same or similar to the components of living teeth and bones,
It has the advantage of being a preferred material with little rejection from living organisms. Among these materials, calcium phosphate-based crystallized glass is expected to be used as a dental material because it has excellent moldability, and in particular, its physical properties closely resemble those of natural teeth.
従来このような材料を得る手段としては、リン酸マグネ
シウム系の型材や珪酸塩系の型材中にリン酸カルシウム
系材料を鋳込んで成形及び結晶化が行なわれていた。Conventionally, such a material has been obtained by casting a calcium phosphate-based material into a magnesium phosphate-based mold material or a silicate-based mold material, followed by molding and crystallization.
[発明の解決しようとする問題点]
しかしながら、これらは何れも型材の表面に微細なりラ
ックが発生したり、型材の強度が不十分である為、成形
時におけるガラスの流入により一部型崩れを生じたりし
、得られたガラス成形体の表面に突起やパリ等が発生し
1寸法精度が非常に不安定である欠点を有していた。[Problems to be Solved by the Invention] However, in all of these methods, fine cracks or racks occur on the surface of the mold material, and the strength of the mold material is insufficient, so that the shape may partially collapse due to the inflow of glass during molding. This has the drawback that protrusions, cracks, etc. occur on the surface of the obtained glass molded product, and the one-dimensional accuracy is extremely unstable.
[問題点を解決するための手段]
本発明者は従来法が有する欠点を排除し、成形体表面に
微細なりラックを生じることなく、又寸法精度のよい成
形体を成形し得る型を見出すことを目的として種々研究
、検討した結果、型の成形面付近に特定の処理を施すこ
とにより、前記目的を達成し得ることを見出した。かく
して本発明は、型の成形面から少なくとも10川の深さ
迄耐熱性を有する#a維状状物質存在せしめた成形用型
及び、更に窒化ホウ素を併用することにより類型の成形
面から成形物を容易に’A#せしめることのできる成形
用型を提供するにある。[Means for Solving the Problems] The inventor of the present invention aims to eliminate the drawbacks of conventional methods and to find a mold capable of molding a molded product with good dimensional accuracy without producing fine racks on the surface of the molded product. As a result of various studies and examinations aimed at this purpose, it has been found that the above object can be achieved by applying a specific treatment to the vicinity of the molding surface of the mold. Thus, the present invention provides a mold in which #a fibrous material having heat resistance exists from the molding surface of the mold to a depth of at least 10 mm, and a molded product from the molding surface of the same type by using boron nitride in combination. The object of the present invention is to provide a molding die that can easily give 'A#.
本発明において、RH状物質を存在せしめる為の型基材
としては特に限定されず、例えばリン酸マグネシウム系
、珪酸塩系、アルミナ系、リン酸アルミニウム系、ジル
コニア系1石腎系等を適宜採用し得る。In the present invention, the mold base material for making the RH-like substance exist is not particularly limited, and for example, magnesium phosphate, silicate, alumina, aluminum phosphate, zirconia, etc. are appropriately used. It is possible.
繊維状物質の性状としては、直径が0.1〜10g、l
さが10〜500 tLを採用するのが適当である。直
径が0゜lJLに満たない場合には1期待すべき効果が
十分発揮されず、逆に前記範囲を超える場合には型の成
形表面の平滑性が損われる恐れがあり、何れも好ましく
ない、又、長さが10μに満たない場合には、期待すべ
き効果が十分発揮されず、逆に前記範囲を超える場合に
は型の成形表面の平滑性が損われる恐れがあるので、何
れも好ましくない。The properties of the fibrous material include a diameter of 0.1 to 10 g, l
It is appropriate to adopt a length of 10 to 500 tL. If the diameter is less than 0°lJL, the expected effect will not be fully exhibited, and if it exceeds the above range, the smoothness of the molding surface may be impaired, both of which are undesirable. In addition, if the length is less than 10μ, the expected effect will not be fully exhibited, and if it exceeds the above range, the smoothness of the molding surface of the mold may be impaired, so both are preferred. do not have.
そしてこれら範囲のうち、直径が0.2〜2ル、長さが
20〜200川を採用する場合には、初期の目的を十分
達成し得るので特に好ましい。Among these ranges, it is particularly preferable to adopt a diameter of 0.2 to 2 mm and a length of 20 to 200 mm, since the initial purpose can be sufficiently achieved.
又、このような繊維は型の表面から少なくとも1111
stの深さ迄存在せしめることが必要である。Also, such fibers are at least 1111 from the surface of the mold.
It is necessary to make it exist up to the depth of st.
存在させる深さが101Lに満たない場合には、初期の
効果を得ることができないので不適当である。実際型を
作成する際には、型基材原料と共にm雄を混合し、型全
体にわたって繊維を存在せしめてしまうのが現実的であ
るが、本質的には型の表面から50μ程度迄繊維を存在
せしめれば初期の目的を十分且つ安定して得ることがで
きる。型に存在せしめる繊維の量は、これが存在せしめ
られる深さまでの型基材の量と繊維の量の総量に対し、
0.5〜30重量%を採用するのが適当である。存在量
が前記範囲に満たない場合には初期の目的を十分達成し
得す、逆に前記範囲を超える場合には成形表面の平滑性
が損われる恐れがあるので何れも好ましくない、そして
これら範囲のうち、1〜10重量%を採用する場合には
、初期の目的を十分達成し得ると共に、成形体表面の平
滑性も損われないので特に好ましい。If the depth is less than 101L, it is not appropriate because the initial effect cannot be obtained. When making an actual mold, it is practical to mix m-mole with the raw material for the mold base material so that the fibers are present throughout the entire mold, but essentially the fibers are removed from the surface of the mold to about 50μ. If it exists, the initial purpose can be achieved sufficiently and stably. The amount of fibers to be present in the mold is based on the total amount of the mold base material and the amount of fibers up to the depth at which the fibers are present.
It is appropriate to employ 0.5 to 30% by weight. If the amount is less than the above range, the initial purpose can be sufficiently achieved; conversely, if it exceeds the above range, the smoothness of the molded surface may be impaired, so both are unfavorable. It is particularly preferable to use 1 to 10% by weight, since the initial objective can be sufficiently achieved and the smoothness of the surface of the molded article will not be impaired.
本発明に用いられる繊維状物質は、被成形体が頭初溶融
物である為、耐熱性であることが要求され、具体的には
800°C以上の高温下で安定なものであれば特に制限
はない、そのような繊維としては、例えば炭化珪素、窒
化珪素、炭化ホウ素、石綿、アルミナ、ロックウール、
シリカ等が挙げられる。かくして本発明による成形用型
を用いて成形された成形物は、表面が平滑であり、突起
やパリの発生がなく、寸法精度も高いが、これだけでは
Ill型性にやや難点がある。特に被成形体がリン酸カ
ルシウム系のガラスの場合には、型とガラスとが一部反
応を起し、離型が困難となる傾向がある。The fibrous material used in the present invention is required to be heat resistant because the object to be molded is initially melted, and specifically, if it is stable at high temperatures of 800°C or higher, Without limitation, such fibers include, for example, silicon carbide, silicon nitride, boron carbide, asbestos, alumina, rock wool,
Examples include silica. Thus, the molded product molded using the mold according to the present invention has a smooth surface, no protrusions or cracks, and has high dimensional accuracy, but this alone has some drawbacks in Ill moldability. In particular, when the object to be molded is calcium phosphate glass, there is a tendency for the mold and glass to partially react, making it difficult to release from the mold.
本発明者は、かかる点を改良する為検討を行なった処、
型の表面に窒化ホウ素を存在せしめることにより、離型
性が改善されることを見出した。窒化ホウ素は、前述の
繊維状物質と同様に型の表面から少なくとも10μの深
さ迄存在せしめればよい。The inventor conducted studies to improve this point, and found that
It has been found that the presence of boron nitride on the surface of the mold improves mold release properties. The boron nitride may be present to a depth of at least 10 μm from the surface of the mold, similar to the aforementioned fibrous material.
窒化ホウ素とm雄状物質の使用量は、これらとこれらが
存在する型基材の総量に対し、窒化ホウ素が10〜80
重量%、m雄状物質が0.5〜30重量%を採用するの
が適当である。The amount of boron nitride and male substance used is 10 to 80% of the total amount of boron nitride and the mold base material in which they are present.
It is appropriate to employ 0.5 to 30% by weight of the male substance.
窒化ホウ素の使用量が前記範囲に満たない場合には、十
分な離型効果を期待できず、逆に前記範囲を超える場合
には、型の強度が低下し、繊維状物質を存在せしめるこ
との意味がなくなる恐れがあるので何れも好ましくない
。If the amount of boron nitride used is less than the above range, a sufficient mold release effect cannot be expected; on the other hand, if it exceeds the above range, the strength of the mold will decrease and fibrous substances may be present. None of these are desirable because they may lose their meaning.
そしてこれら範囲のうち、前記表示に従い、窒化ホウ素
が30〜80重量%、繊維状物質1〜10重量%を採用
すると成形体表面の平滑性も良好であり、且つは型性も
十分なので特に好ましい、実際本発明による成形用型を
得る手段としては、例えば前記のH&雄状物質或はこれ
と窒化ホウ素を型基材に所定量予め混入せしめ、型面の
原型上で硬化させて鋳型を形成する方法、予め作成して
おいた型の表面に前記繊維状物質或はこれと窒化ホウ素
を混入した基材を塗布する方法、型面の原型(ロストワ
ックス法の場合はワックスパターン)面上に、前記繊維
状物質或はこれと窒化ホウ素を混入した基材を塗布した
り浸漬したりすることにより、繊維状物質或はこれと窒
化ホウ素を含有する層を形成した後。Among these ranges, it is particularly preferable to adopt boron nitride in an amount of 30 to 80% by weight and fibrous material in an amount of 1 to 10% by weight, as the surface smoothness of the molded product is good and the moldability is also sufficient. In fact, as a means for obtaining a mold according to the present invention, for example, a predetermined amount of the above-mentioned H&male substance or this and boron nitride is mixed into a mold base material in advance, and the mixture is hardened on the master surface of the mold to form a mold. A method of applying the above-mentioned fibrous material or a base material mixed with boron nitride to the surface of a mold prepared in advance, and applying the fibrous material or a base material mixed with boron nitride to the surface of the original mold surface (wax pattern in the case of the lost wax method). , after forming a layer containing the fibrous material or the boron nitride by coating or dipping the substrate containing the fibrous material or the boron nitride;
型を作成する方法も採用し得る。A method of creating a mold may also be adopted.
本発明による成形用型を用いて成形される材料は種々の
ものが採用されるが、特に生体材料として有用なリン酸
カルシウム系ガラスが適している。その組成としては例
えばCa041〜48.5モル%、P2O558,5〜
50モル%、Al2O30,5〜5モル%であり、且つ
Ga/Pで示される原子比が0.35〜0.7、好まし
くは0.35〜0.48のものが好適である。Although various materials can be used for molding using the mold according to the present invention, calcium phosphate glass, which is useful as a biomaterial, is particularly suitable. Its composition is, for example, Ca041~48.5 mol%, P2O558,5~
50 mol%, Al2O30.5 to 5 mol%, and the atomic ratio represented by Ga/P is 0.35 to 0.7, preferably 0.35 to 0.48.
又、このようなリン酸カルシウム系ガラスを本発明によ
る成形用型を用いて成形する手段としては、例えば通常
行なわれているロストワックス法やプレス成形等の手段
を適宜採用し得る。又、このように形成されたガラスは
更に結晶化することができ、その場合には、例えば70
0℃に保たれた電気炉中に2時間程度保持する等の手段
が採用される。Further, as a means for molding such a calcium phosphate glass using the mold according to the present invention, for example, commonly used means such as the lost wax method or press molding can be appropriately employed. Also, the glass thus formed can be further crystallized, in which case it can be crystallized, e.g.
A method such as keeping the material in an electric furnace maintained at 0° C. for about 2 hours is employed.
[実施例]
実施例1
歯冠の形状をしたワックスパターンにスプルー線をとり
つけ、ゴム製のコーンにセットした。そして直径2〜4
p、長さが100芦程度のアスベスト1部にリン酸塩系
埋没材(徳山曹達社製ブルーベスト)の粉末20部及び
これの専用液40部を加えてスラリーを得、これを前記
ワックスパターン上に塗布し、 0.2+u+程度の厚
さを有する型材表面層を形成せしめた。この全体を金属
製リング中に収め、リン酸塩系埋没材(徳山曹達社製ブ
ルーベスト)によって埋没せしめた0次いでこれを乾燥
後、700℃に加熱してワックスパターンを焼却し、歯
冠作成用ロストワックス型を得た。[Examples] Example 1 A sprue wire was attached to a wax pattern in the shape of a tooth crown, and set in a rubber cone. and diameter 2-4
P, 20 parts of powder of phosphate-based investment material (Blue Best, manufactured by Tokuyama Soda Co., Ltd.) and 40 parts of its special solution are added to 1 part of asbestos with a length of about 100 reeds to obtain a slurry, and this is used to form the wax pattern. A mold surface layer having a thickness of about 0.2+u+ was formed. The whole was placed in a metal ring and buried with a phosphate-based investment material (Blue Best, manufactured by Tokuyama Soda).Then, after drying, the wax pattern was burned off by heating to 700°C to create a dental crown. A lost wax mold was obtained.
他方、Ca024重量%、Al2O31重量%、220
575重量%の組成物を1250°Cにて溶融し、ガラ
ス融液を得、これを前記ロストワックス型に遠心鋳造し
、そのまま680℃に3時間保持せしめて結晶化を行な
った。On the other hand, Ca024% by weight, Al2O31% by weight, 220
A 575% by weight composition was melted at 1250°C to obtain a glass melt, which was centrifugally cast into the lost wax mold and kept at 680°C for 3 hours to effect crystallization.
次いで型をこわして成形体をとり出し、スプルー線を切
断してリン酸カルシウム結晶化ガラス製歯冠な得た。得
られた歯冠は、表面光沢はないものの、突起やパリ等は
認められず、軽い研磨で光沢を持つ表面が得られた。こ
の歯冠のワックスパターンとの寸法変化は50μ以下で
あった・
実施例2
直径0.5〜2μ、長さ20〜100終程度の炭化珪素
ウィスカー2部を窒化ホウ素粉末10部、エチルシリケ
ート系バインダー(コルコート社製HAS−8) 15
部と混合して均一なスラリーを得、これを実施例1と同
様に用意したワックスノくターン上に塗布し、0.2部
前後の厚さを有す型材表面層を形成し起、以下実施例1
と同様にしてリン酸カルシウム結晶化ガラス製歯冠を得
た。Next, the mold was broken and the molded body was taken out, and the sprue wire was cut to obtain a dental crown made of calcium phosphate crystallized glass. Although the obtained tooth crown did not have a glossy surface, no protrusions or cracks were observed, and a glossy surface was obtained by light polishing. The dimensional change of this tooth crown with the wax pattern was 50 μ or less. Example 2 2 parts of silicon carbide whiskers with a diameter of 0.5 to 2 μ and a length of about 20 to 100 μm were mixed with 10 parts of boron nitride powder and ethyl silicate. Binder (HAS-8 manufactured by Colcoat) 15
A homogeneous slurry was obtained by mixing 1 part with 1 part of wax, and this was applied onto the wax turn prepared in the same manner as in Example 1 to form a surface layer of the mold material having a thickness of about 0.2 parts. Example 1
A dental crown made of calcium phosphate crystallized glass was obtained in the same manner as above.
得られた歯冠の表面は非常に滑らかで光沢をもち、バリ
ヤ突起は全く存在しなかった。又。The surface of the resulting tooth crown was very smooth and shiny, and no barrier protrusions were present. or.
Claims (1)
有する繊維状物質を存在せしめたことを特徴とする成形
用型。 2、繊維状物質は、直径0.1〜10μ、長さ10〜5
00μである請求の範囲(1)の成形用型。 3、型の成形面から少なくとも10μの深さ迄耐熱性を
有する繊維状物質と窒化ホウ素とを存在せしめたことを
特徴とする成形用型。 4、繊維状物質と窒化ホウ素の存在量は、これらとこれ
らが存在する型基材の総量に対し、前者が0.5〜30
重量%、10〜80重量%である特許請求の範囲(3)
の成形用型。 5、繊維状物質は、直径0.1〜10μ、長さ10〜5
00μである特許請求の範囲(3)又は(4)の成形用
型。[Scope of Claims] 1. A mold for molding, characterized in that a fibrous material having heat resistance is present to a depth of at least 10 μm from the molding surface of the mold. 2. The fibrous substance has a diameter of 0.1 to 10 μm and a length of 10 to 5 μm.
00μ, the mold according to claim (1). 3. A mold for molding, characterized in that a fibrous substance having heat resistance and boron nitride are present to a depth of at least 10 μm from the molding surface of the mold. 4. The amount of fibrous substances and boron nitride present is 0.5 to 30% of the total amount of these and the mold base material in which they exist.
Claim (3) % by weight, 10-80% by weight
mold for molding. 5. The fibrous substance has a diameter of 0.1 to 10 μm and a length of 10 to 5 μm.
00μ, the mold according to claim (3) or (4).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24409486A JPH0787848B2 (en) | 1986-10-16 | 1986-10-16 | Mold for molding |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24409486A JPH0787848B2 (en) | 1986-10-16 | 1986-10-16 | Mold for molding |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6399859A true JPS6399859A (en) | 1988-05-02 |
JPH0787848B2 JPH0787848B2 (en) | 1995-09-27 |
Family
ID=17113655
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP24409486A Expired - Fee Related JPH0787848B2 (en) | 1986-10-16 | 1986-10-16 | Mold for molding |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0787848B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001021088A1 (en) * | 1999-09-20 | 2001-03-29 | Tokuyama Corporation | Method of producing ceramic crowns and production kit used therefor |
JP2006117525A (en) * | 2004-10-21 | 2006-05-11 | Schott Ag | Method and device for casting glass block |
JP2008056322A (en) * | 2006-09-01 | 2008-03-13 | Key Tranding Co Ltd | Container with cap |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5542938A (en) * | 1978-09-20 | 1980-03-26 | Shinnitsukei Jiyuutaku Kenzai | Method of working outside corner of buildeng |
JPS61140344A (en) * | 1984-12-14 | 1986-06-27 | Mitsubishi Heavy Ind Ltd | Manufacture of mold |
-
1986
- 1986-10-16 JP JP24409486A patent/JPH0787848B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5542938A (en) * | 1978-09-20 | 1980-03-26 | Shinnitsukei Jiyuutaku Kenzai | Method of working outside corner of buildeng |
JPS61140344A (en) * | 1984-12-14 | 1986-06-27 | Mitsubishi Heavy Ind Ltd | Manufacture of mold |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001021088A1 (en) * | 1999-09-20 | 2001-03-29 | Tokuyama Corporation | Method of producing ceramic crowns and production kit used therefor |
JP2006117525A (en) * | 2004-10-21 | 2006-05-11 | Schott Ag | Method and device for casting glass block |
JP4560474B2 (en) * | 2004-10-21 | 2010-10-13 | ショット アクチエンゲゼルシャフト | Method and apparatus for casting glass blocks |
JP2008056322A (en) * | 2006-09-01 | 2008-03-13 | Key Tranding Co Ltd | Container with cap |
Also Published As
Publication number | Publication date |
---|---|
JPH0787848B2 (en) | 1995-09-27 |
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