JPS6219236A - Dispersing method of boron nitride into base material - Google Patents

Dispersing method of boron nitride into base material

Info

Publication number
JPS6219236A
JPS6219236A JP15511485A JP15511485A JPS6219236A JP S6219236 A JPS6219236 A JP S6219236A JP 15511485 A JP15511485 A JP 15511485A JP 15511485 A JP15511485 A JP 15511485A JP S6219236 A JPS6219236 A JP S6219236A
Authority
JP
Japan
Prior art keywords
boron nitride
base material
surfactant
dispersion method
mold
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.)
Pending
Application number
JP15511485A
Other languages
Japanese (ja)
Inventor
Shigeyoshi Kobayashi
小林 重義
Tsuneo Manabe
恒夫 真鍋
Yasuko Osaki
康子 大崎
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.)
AGC Inc
Original Assignee
Asahi Glass Co Ltd
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 Asahi Glass Co Ltd filed Critical Asahi Glass Co Ltd
Priority to JP15511485A priority Critical patent/JPS6219236A/en
Publication of JPS6219236A publication Critical patent/JPS6219236A/en
Pending legal-status Critical Current

Links

Landscapes

  • Colloid Chemistry (AREA)

Abstract

PURPOSE:To increase the dispersion properties and also to prevent the reflocculation by dispersing boron nitride for a base material such as gypsum in the presence of a surfactant. CONSTITUTION:A uniformly mixed slurry is easily obtained by mixing 1-90wt% boron nitride and 0.001-10wt% surfactant as a mold release agent to a base material for a mold such as gypsum and silica and stirring the mixture. Further as the surfactant, the effect is recognized in spite of the kind but especially an anionic and a nonionic surfactants are effective. In case of the nonionic surfactant, HLB is at least 5 and preferably >=8.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、基材中への窒化ホウ素の分散方法。[Detailed description of the invention] (Industrial application field) The present invention is a method for dispersing boron nitride into a substrate.

特に鋳型表面に離型材として存在せしめる窒化ホウ素の
分散性を向上せしめる方法に係るものである。
In particular, the present invention relates to a method for improving the dispersibility of boron nitride present as a mold release material on the surface of a mold.

(従来の技術) 各種鋳型表面は、鋳造物との離型性が高いことが必要で
あり、この為各種の離型手段が提案されている。
(Prior Art) It is necessary for the surfaces of various molds to have high mold releasability from the cast product, and for this purpose various mold release means have been proposed.

これら手段の中には窒化ホウ素の層を設けることが種々
の鋳型に対し提案され、又一部は実施されている。
Among these measures, the provision of a layer of boron nitride has been proposed, and some have been implemented, for various molds.

(発明の解決しようとする問題点) 窒化ホウ素は表面滑性が太きく、又化学的に安定である
為、応用範囲が広い利点がある反面、他の材料に対する
分散性が悪い欠点を有している。
(Problems to be solved by the invention) Boron nitride has a large surface smoothness and is chemically stable, so it has the advantage of having a wide range of applications, but has the disadvantage of poor dispersibility in other materials. ing.

例えば、石膏スラリー等の基材に対し、少量の粉末状窒
化ホウ素を分散させるような典型例においても、その均
一分散には多大なエネルギーと時間を要すると共に1分
散した。スラリーの粘度がかなり高くなり、その後の成
形操作が困難になったり、又微細な気泡を多量に包含す
る為、成形体にそのまま泡による欠点が生じる等種々の
障害や欠点を有していた。更には、この様にして分散せ
しめた窒化ホウ素粉末は再凝集し易く、窒化ホウ素の添
加効果がそれ程有効でない等の欠点もある。
For example, even in a typical case where a small amount of powdered boron nitride is dispersed in a base material such as gypsum slurry, it takes a great deal of energy and time to uniformly disperse the powder, and only one dispersion is required. The viscosity of the slurry becomes quite high, making the subsequent molding operation difficult, and since it contains a large amount of fine bubbles, the molded product itself has various problems and defects, such as defects caused by the bubbles. Furthermore, the boron nitride powder dispersed in this manner is likely to reagglomerate, and the effect of adding boron nitride is not very effective.

(問題点を解決する為の手段) 本発明者は、これら諸欠点を解消し、窒化ホウ素を基材
中に容易に且均−に分散せしめ、しかも分散後の窒化ホ
ウ素が再凝集を起すことがないようにせしめるf段を見
出すことを目的として種々研究、検討した結果、窒化ホ
ウ素を界面活性剤の存在下に分散せしめることにより、
前記目的を達成し得ることを見出し1本発明はこれを要
旨とするものである。
(Means for Solving the Problems) The present inventor has solved these various drawbacks, made boron nitride easily and uniformly dispersed in the base material, and furthermore, the boron nitride after dispersion does not cause re-agglomeration. As a result of various studies and examinations aimed at finding an f-stage that eliminates the
It has been found that the above object can be achieved, and this is the gist of the present invention.

本発明において窒化ホウ素が分散される基材としては、
例えば1石膏、シリカ、リン酸マグネシウム、リン酸ア
ルミニウム、酸化マグネシウム。
In the present invention, the base material in which boron nitride is dispersed includes:
For example, 1 gypsum, silica, magnesium phosphate, aluminum phosphate, magnesium oxide.

ケイ酸カルシウム等であり、これらは歯科材料としての
埋没材、金属等の鋳型、ルツボ、潤滑材等に用いられる
材料が挙げられる。
Calcium silicate, etc., and these include materials used for dental investment materials, metal molds, crucibles, lubricants, and the like.

この様な基材中に分散される窒化ホウ素の量は、これが
鋳型等の表面滑性を付与せしめる場合、混合される基材
100g (乾燥量)当り 1〜90g程度を採用する
のが適当である。
The amount of boron nitride dispersed in such a base material is preferably about 1 to 90 g per 100 g (dry amount) of the base material to be mixed, when it imparts surface smoothness to a mold, etc. be.

本発明において、基材に対して窒化ホウ素を分散せ−し
める際、界面活性剤が用いられる。用いられる界面活性
剤の量は、一般に基材に対しo、oot〜10重量%を
採用することにより、容易且均−に窒化ホウ素を基材中
に分散せしめ得ると共に1分散後の窒化ホウ素の凝集を
も十分に抑制することが出来る。
In the present invention, a surfactant is used when dispersing boron nitride into the base material. The amount of surfactant to be used is generally from o,oot to 10% by weight based on the base material, so that boron nitride can be easily and uniformly dispersed in the base material and the amount of boron nitride after dispersion can be reduced. Aggregation can also be sufficiently suppressed.

かかる界面活性剤としては、その種類によらず効果は認
められるが、特にアニオン系界面活性剤、非イオン系界
面活性剤を採用すると高い効果を期待し得る。
Although such surfactants are effective regardless of their type, particularly high effects can be expected when anionic surfactants and nonionic surfactants are employed.

用いられるアニオン系界面活性剤としては例えば、高級
アルコール硫酸エステル塩系、脂肪酸塩系、アルキルベ
ンゼンスルホン酸塩系等を、又非イオン系界面活性剤と
しては例えば、ポリオキシエチレンアルキルエーテル、
ポリオ午シエチレンンルビタン脂肪酸エステル等を適宜
採用し得る。
Examples of anionic surfactants used include higher alcohol sulfate ester salts, fatty acid salts, alkylbenzenesulfonate salts, and nonionic surfactants such as polyoxyethylene alkyl ether,
Polyoxyethylene rubitan fatty acid ester and the like may be appropriately employed.

そして非イオン界面活性剤を採用する場合、そのHLB
が少なくとも5、好ましくは8以りを採用すると高い効
果を期待し得る。
When using a nonionic surfactant, its HLB
When the ratio is at least 5, preferably 8 or more, high effects can be expected.

基材中に分散される窒化ホウ素は、使用目的に応じ、基
材の全体中に分散されたり、或は例えば鋳型のように被
成形物と接触する型面付近に集中的に分散する等種々の
態様を採用し得る。
Depending on the purpose of use, boron nitride can be dispersed throughout the base material, or it can be concentrated in the vicinity of the mold surface that comes into contact with the object to be molded, such as in a casting mold. The following aspect may be adopted.

尚、本発明において基材として前述の如き材料を用い得
るが、この他例えばエチルシリケート等の基材に対する
バインダーや増量剤、充填材1着色剤等を本発明の目的
を阻害しない限り適宜併用することが出来る。
In addition, in the present invention, the above-mentioned materials can be used as the base material, but in addition, binders and extenders for the base material such as ethyl silicate, filler 1 colorants, etc. may be used in combination as appropriate as long as they do not impede the purpose of the present invention. I can do it.

(実施例) 実施例1 非イオン系界面活性剤(三洋化成社製ノニポール55、
HL B  10.5)0.5gを添加したシリカゾル
を主剤とする埋没材専用液100gに、り酸塩系埋没材
(徳山金遣社製ブルーベスト)粉末100g及び窒化ホ
ウ素粉末40gを加え、ヨシダ社製つ′アキューミナ型
攪拌機を用いてtOtorrの真空下で740rpmに
て20秒間攪拌、脱泡した処、均一に混合された滑らか
なスラリーを得た。そして、中心部に山型ワックスパタ
ーンを植立てたリング中に前記脱泡スラリーを充填し、
硬化せしめた。
(Example) Example 1 Nonionic surfactant (Nonipol 55 manufactured by Sanyo Chemical Co., Ltd.
HL B 10.5) 0.5g) was added to 100g of a dedicated investment material solution containing silica sol as the main ingredient, 100g of phosphate-based investment material (Blue Best manufactured by Tokuyama Kinken Co., Ltd.) powder and 40g of boron nitride powder were added, and Yoshida The mixture was stirred and degassed for 20 seconds at 740 rpm under a vacuum of tOtorr using a Tsu'acumina type stirrer manufactured by Kogyo Co., Ltd., to obtain a uniformly mixed and smooth slurry. Then, the defoamed slurry is filled into a ring with a chevron-shaped wax pattern planted in the center,
Hardened.

次いでこれらを700℃にて1時間加熱してワックスパ
ターンを焼却してそこに空洞を得た。一方、 CaO2
5重量%、Al2O32重量%、P2O573重量%か
ら成る組成物を1250℃で溶融せしめ、これを遠心鋳
造法により前記空洞へ導入して鋳造し、700℃に2時
間保持せしめて結晶化したガラスを得た。その後これを
1時間かけて冷却し、型をこわして結晶化ガラス成形体
を取り出し、歯ブラシをかけた処、付着した埋没材は全
て容易に!A離し、成形体表面には型材との反応部分は
全く認められず、半透明銭を持つ白色の成形体が得られ
た。
These were then heated at 700° C. for 1 hour to burn out the wax pattern and obtain cavities therein. On the other hand, CaO2
A composition consisting of 5% by weight, 2% by weight of Al2O, and 573% by weight of P2O was melted at 1250°C, introduced into the cavity by centrifugal casting, cast, and kept at 700°C for 2 hours to form a crystallized glass. Obtained. After that, I cooled it down for an hour, broke the mold, took out the crystallized glass molded body, and brushed it with a toothbrush. All the investment material that had adhered to it was easily removed! After separating A, no reaction area with the molding material was observed on the surface of the molded product, and a white molded product with translucent texture was obtained.

実施例2 アニオン系界面活性剤(化上社製ネオペレックス) 0
.01g及び窒化ホウ素粉末5gを添加分散せしめたシ
リカゾルを主剤とした埋没材専用液15gに、リン酸塩
系埋没材(8山背達社製ブルーベスト)粉末10gを添
加し、実施例1と同様な攪拌機を用い、 ?40rps
+にて20秒間攪拌、真空脱泡した処、均一・に混合さ
れた滑らかなスラリーを得た。
Example 2 Anionic surfactant (Neoperex manufactured by Kajosha) 0
.. 10 g of phosphate-based investment material (Blue Best manufactured by Yayama Seidai Co., Ltd.) powder was added to 15 g of a dedicated investment material solution mainly composed of silica sol in which 01 g of boron nitride powder and 5 g of boron nitride powder were added and dispersed. Using a stirrer, ? 40rps
After stirring at + for 20 seconds and defoaming under vacuum, a smooth, uniformly mixed slurry was obtained.

かかるスラリーを、予めゴム製のコーンtにセットした
スプルー線りに固定した歯型ワックスパターンの表面に
厚さが0.1〜0.5層鵬になるよう塗布した。そして
、このワックスパターンをリング中心部に積立て、該リ
ング中にリン酸塩系埋没材(徳山汀達社製ブルーベスト
)のスラリーを充填し、硬化せしめた。
This slurry was applied to the surface of a tooth-shaped wax pattern fixed to a sprue wire set in advance in a rubber cone T to a thickness of 0.1 to 0.5 layers. Then, this wax pattern was stacked at the center of the ring, and a slurry of a phosphate-based investment material (Blue Best, manufactured by Tokuyama Teidai Co., Ltd.) was filled into the ring and allowed to harden.

次いで実施例1と同様に熱処理、ガラスの鋳造成形、結
晶化を行ない、成形体を得た。得られた成形体は実施例
1と同様に型材との反応は全くなく、同様な外観を呈し
ていた。
Next, heat treatment, glass casting, and crystallization were performed in the same manner as in Example 1 to obtain a molded body. As in Example 1, the obtained molded product had no reaction with the mold material and had the same appearance.

比較例 界面活性剤を用いない以外は実施例1と同様にして埋没
材スリラーを得ようとして同様に攪拌を行なった処、2
分間かかってようやくほぼ均一と思われるかなり粘りの
あるスラリーを得た。
Comparative Example The same procedure as in Example 1 was carried out except that no surfactant was used, and stirring was carried out in the same manner as in Example 1.
After a few minutes, I finally got a fairly sticky slurry that appeared to be almost homogeneous.

かかるスラリーを用いて実施例1と同様にしてガラス成
形体を得た処、成形体表面の数ケ所に80μ前後の不規
則な突起状をした型材との反応生成物が存在していた。
When a glass molded body was obtained using this slurry in the same manner as in Example 1, there were reaction products with the mold material in the shape of irregular protrusions of about 80 μm at several places on the surface of the molded body.

これは型材に一部窒化ホウ素が分散していない為であり
、又その部分の型材が欠損していた。これらのことから
均一な埋没材スラリーが生成していないか若しくは一度
生成した均一スラリー中の窒化ホウ素が一部再凝集を起
したものと思われる。               
  r手続補正書(方式゛ 昭和 60年11 JJlq日
This is because some boron nitride was not dispersed in the mold material, and that portion of the mold material was missing. From these facts, it seems that either a uniform investment material slurry was not produced, or that some of the boron nitride in the uniform slurry that was once produced re-agglomerated.
r Procedural amendment (formula, Showa 60, 11 JJlq

Claims (1)

【特許請求の範囲】 1、基材に対し、窒化ホウ素を界面活性剤の存在下に分
散せしめることを特徴とする基材中への窒化ホウ素の分
散方法。 2、基材中に分散される窒化ホウ素の量は、基材に対し
1〜90重量%である特許請求の範囲(1)の分散方法
。 3、界面活性剤の存在量は、基材に対し0.001〜1
0重量%である特許請求の範囲(1)の分散方法。 4、基材は石膏、シリカ、リン酸マグネシウム、リン酸
アルミニウム、酸化マグネシウ ム、ケイ酸カルシウムである特許請求の範囲(1)の分
散方法。 5、界面活性剤は、アニオン系界面活性剤である特許請
求の範囲(1)又は(3)の分散方法。 6、界面活性剤は、非イオン系界面活性剤である特許請
求の範囲(1)又は(3)の分散方法。 7、非イオン系界面活性剤は、そのHLBが少なくとも
5である特許請求の範囲(6)の分散方法。
[Claims] 1. A method for dispersing boron nitride into a substrate, which comprises dispersing boron nitride into the substrate in the presence of a surfactant. 2. The dispersion method according to claim (1), wherein the amount of boron nitride dispersed in the base material is 1 to 90% by weight based on the base material. 3. The amount of surfactant present is 0.001 to 1% relative to the base material.
The dispersion method according to claim (1), wherein the dispersion method is 0% by weight. 4. The dispersion method according to claim (1), wherein the base material is gypsum, silica, magnesium phosphate, aluminum phosphate, magnesium oxide, or calcium silicate. 5. The dispersion method according to claim (1) or (3), wherein the surfactant is an anionic surfactant. 6. The dispersion method according to claim (1) or (3), wherein the surfactant is a nonionic surfactant. 7. The dispersion method according to claim (6), wherein the nonionic surfactant has an HLB of at least 5.
JP15511485A 1985-07-16 1985-07-16 Dispersing method of boron nitride into base material Pending JPS6219236A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15511485A JPS6219236A (en) 1985-07-16 1985-07-16 Dispersing method of boron nitride into base material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15511485A JPS6219236A (en) 1985-07-16 1985-07-16 Dispersing method of boron nitride into base material

Publications (1)

Publication Number Publication Date
JPS6219236A true JPS6219236A (en) 1987-01-28

Family

ID=15598890

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15511485A Pending JPS6219236A (en) 1985-07-16 1985-07-16 Dispersing method of boron nitride into base material

Country Status (1)

Country Link
JP (1) JPS6219236A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017130647A1 (en) * 2016-01-26 2017-08-03 株式会社ジーシー Dental investment material

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4911919A (en) * 1972-05-13 1974-02-01
JPS52108323A (en) * 1976-03-10 1977-09-10 Showa Denko Kk High temperature lubricant parting agent composition
JPS55149746A (en) * 1979-05-10 1980-11-21 Chuo Hatsumei Kenkyusho:Kk Durable coat for metal mold casting
JPS5748297A (en) * 1980-09-04 1982-03-19 Mitsubishi Electric Corp Hybrid integrated circuit

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4911919A (en) * 1972-05-13 1974-02-01
JPS52108323A (en) * 1976-03-10 1977-09-10 Showa Denko Kk High temperature lubricant parting agent composition
JPS55149746A (en) * 1979-05-10 1980-11-21 Chuo Hatsumei Kenkyusho:Kk Durable coat for metal mold casting
JPS5748297A (en) * 1980-09-04 1982-03-19 Mitsubishi Electric Corp Hybrid integrated circuit

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017130647A1 (en) * 2016-01-26 2017-08-03 株式会社ジーシー Dental investment material
CN108601709A (en) * 2016-01-26 2018-09-28 株式会社Gc Dental embedded material

Similar Documents

Publication Publication Date Title
US10532953B2 (en) Precursor material for additive manufacturing of low-density, high-porosity ceramic parts and methods of producing the same
KR910001026A (en) Formation of detergent granules by deagglomeration of detergent powder
JPS59227794A (en) Ceramic fiber composition
US1909008A (en) Highly refractory denial mold material and method of making the same
JPS6287427A (en) Mold material
US3303030A (en) Refractory mold
JPH04214763A (en) Thermosettinmg molding composition of silicone resin
TR26051A (en) A PROCESS FOR THE PREPARATION OF CONCENTRATED LIQUID DETERGENT COMPOUNDS INCLUDING MAGNESIUM ALKILBENZEN SULFONIC ACID AND ALKANOLAMIDE.
US4662924A (en) Method for molding calcium phosphate type glass
JP2793744B2 (en) Curing agent for impression material
JPH08104535A (en) Release material slurry
JPS6410446B2 (en)
CN1658816A (en) Low-dusting investment composition material
WO2001012571A1 (en) Moulding composition
US5026428A (en) Manufacturing plaster articles
JPS6241190B2 (en)
JP3296474B2 (en) Manufacturing method of curing agent for impression material
JPS6399859A (en) Mold
JPH04356405A (en) Investment for dental precision casting
JPS6139141B2 (en)
US2532155A (en) Thixotropic investment material
SU764828A1 (en) Cold-setting composition for moulds and cores
SU1424937A1 (en) Sand for making moulds and cores
NL1023334C1 (en) Manufacture of heat-resistant mold for manufacturing dental restoration, by preparing slurry from powdered heat-resistant material consisting of powdered particles coated, with hydrophobic material liquid at room temperature, with water
HK1080730A (en) Low-dusting investment composition material