JPS6155579B2 - - Google Patents
Info
- Publication number
- JPS6155579B2 JPS6155579B2 JP56197087A JP19708781A JPS6155579B2 JP S6155579 B2 JPS6155579 B2 JP S6155579B2 JP 56197087 A JP56197087 A JP 56197087A JP 19708781 A JP19708781 A JP 19708781A JP S6155579 B2 JPS6155579 B2 JP S6155579B2
- Authority
- JP
- Japan
- Prior art keywords
- iron
- metal
- compound
- molybdenum
- enstatite
- 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
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 28
- 239000000919 ceramic Substances 0.000 claims description 15
- 239000007788 liquid Substances 0.000 claims description 15
- 229910052634 enstatite Inorganic materials 0.000 claims description 13
- 150000002506 iron compounds Chemical class 0.000 claims description 13
- 235000012222 talc Nutrition 0.000 claims description 13
- 239000000454 talc Substances 0.000 claims description 13
- 229910052623 talc Inorganic materials 0.000 claims description 13
- 239000002131 composite material Substances 0.000 claims description 11
- 229910052742 iron Inorganic materials 0.000 claims description 10
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 8
- 229910052751 metal Inorganic materials 0.000 claims description 7
- 239000002184 metal Substances 0.000 claims description 7
- 239000005078 molybdenum compound Substances 0.000 claims description 7
- 150000002752 molybdenum compounds Chemical class 0.000 claims description 7
- 239000008187 granular material Substances 0.000 claims description 6
- 239000000839 emulsion Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 239000002202 Polyethylene glycol Substances 0.000 claims description 4
- 239000003995 emulsifying agent Substances 0.000 claims description 4
- 229920001223 polyethylene glycol Polymers 0.000 claims description 4
- 239000003125 aqueous solvent Substances 0.000 claims description 3
- 238000003756 stirring Methods 0.000 claims description 3
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical compound ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 230000001590 oxidative effect Effects 0.000 claims description 2
- 239000007921 spray Substances 0.000 claims description 2
- 229950011008 tetrachloroethylene Drugs 0.000 claims description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 6
- 229910052839 forsterite Inorganic materials 0.000 description 5
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 5
- BBCCCLINBSELLX-UHFFFAOYSA-N magnesium;dihydroxy(oxo)silane Chemical compound [Mg+2].O[Si](O)=O BBCCCLINBSELLX-UHFFFAOYSA-N 0.000 description 5
- 229910052750 molybdenum Inorganic materials 0.000 description 4
- 239000011733 molybdenum Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 238000005245 sintering Methods 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 239000000395 magnesium oxide Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000002905 metal composite material Substances 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 229910004298 SiO 2 Inorganic materials 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
- 239000011230 binding agent Substances 0.000 description 2
- 238000010292 electrical insulation Methods 0.000 description 2
- 239000011810 insulating material Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229910052573 porcelain Inorganic materials 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 230000004931 aggregating effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000005524 ceramic coating Methods 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000011246 composite particle Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000017525 heat dissipation Effects 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 238000001465 metallisation Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229910000476 molybdenum oxide Inorganic materials 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
Landscapes
- Powder Metallurgy (AREA)
- Compositions Of Oxide Ceramics (AREA)
Description
本発明は熱伝導度の向上したセラミツクと金属
との複合材料とその製造方法に係り、更に詳しく
は、複合材料の破断面が拡大微視的に、各内核が
鉄あるいは鉄とモリブデン金属であり、その各々
の内核外皮面がフオルステライト―エンスタタイ
ト系皮膜で被覆されて結合し、材料の外表面がフ
オルステライト―エンスタタイト系皮膜層で被覆
された複合材料およびその製造法に関するもので
ある。
従来からフオルステライトやそれと同質のエン
スタタイトセラミツクスがあり、これらのセラミ
ツクスは電気絶縁性に優れ、かつ被メタライズ性
も良好であり、また焼結温度も1200〜1400℃と低
いために、電子部品用絶縁材料として好適であ
る。
しかし乍ら、これらのセラミツクスは熱伝導度
がアルミナあるいはマグネシヤセラミツクスの1/
5〜1/10と低いために熱放散性に劣り、厚膜用IC
基板または抵抗基板としての用途には大きな制約
があつた。
本発明は以上の問題点を解決するために成され
たものであり、その要旨は特許請求の範囲に記載
された内容のセラミツクと金属との複合材料およ
びその製造方法によるものである。
本発明はセラミツクスの電気絶縁性を損うこと
なく、熱伝導率を向上させる方策として、内核が
金属でその核の外皮面がセラミツクスよりなる単
位の構成とした焼結体を得るものでありフオルス
テライトと鉄との熱膨張係数があまり差がないこ
とから両者の複合化が容易であり、かつ鉄と熱膨
張係数の小さいモリブデンとの混合比率を加減す
ることによりフオルステライトとの係数の差を小
さくして複合化するものである。またセラミツク
スと金属との複合粒子を作成するために、鉄化合
物あるいは鉄化合物とモリブデン化合物/滑石タ
イプのエマルジヨンが他種の固形乳化剤よりも有
効であることがテスト結果より判明した。また上
記の金属化合物はセラミツクの焼結温度以下で金
属に還元されることと、また水に分散あるいは溶
解することを考慮すると同時に、金属の融点が磁
器の焼結温度以上であることを条件として選定し
たものである。
以上のもので作成した複合材料の破断面が拡大
微視的に、各内核が鉄金属あるいは鉄とモリブデ
ン金属であり、その各々の内核外皮面がフオルス
テライト―エンスタタイト系セラミツク皮膜で被
覆構成された生成メカニズムについて簡単に説明
すれば、鉄化合物あるいは鉄化合物とモリブデン
化合物との混合物に水とポリエチレングリコール
を加え混合したA混濁液を、非水溶媒に滑石を混
合分散したB混濁液中に注入しつつ強力に撹拌す
ると、A混濁液が微粒子となつて非水溶媒中で分
散する。この場合に滑石はA混濁液微粒子が互に
凝集しないように安定して分散させる乳化剤とし
ての作用を果たし、かつ滑石はA混濁液微粒子の
周囲を取り囲んだ状態である。このエマルジヨン
を噴霧乾燥器にて造粒すると、内核が鉄化合物あ
るいは鉄化合物とモリブデン化合物で、その外皮
面が滑石よりなる顆粒が形成される。この顆粒の
粉末を加圧成形し非酸化性雰囲気中で焼結する
と、滑石の3MgO・4SiO2・H2Oは再結晶化反応
および焼結反応にてフオルステライト2MgO・
SiO2とエンスタタイトMgO・SiO2とガラス質と
なり、一方のFe2O3は還元されてFeとなり、
MoO3はMoとなり所期の複合材料が得られる。こ
の焼結体の破断面を走査型電子顕微鏡で観察して
その構造の拡大微視的に第1図に示し、図中1は
フオルステライト―エンスタタイト系セラミツク
であり、その内部が鉄2あるいは鉄とモリブデン
2との結合した複合材料である。
本発明により得られたセラミツクスと金属との
複合材料は、熱伝導度が室温で0.10ca1/cm・
sec・℃であり、体積固有抵抗が室温で4×1013
Ω・cmであつて、フオルステライトの0.012ca1/
cm・sec・℃と8×1013Ω・cmやエンスタタイト
の0.006ca1/cm・sec・℃と3×1014Ω・cmに比
較して、熱伝導度を大幅に向上することが出来、
その割には体積固有抵抗は低くならず、実用性の
高い材料であつた。
以下、実施例により説明するが、本発明の要旨
を越えない範囲内において、これに限定されな
い。
実施例
酸化第2鉄(Fe2O3,林純薬工業製,試薬1
級)450gと酸化モリブデン(MoO3,米山薬品
工業,試薬1級)286gに対し水1400c.c.と結合剤
として#4000ポリエチレングリコール7gとをア
ルミナ磁器ボールミルにて15時間混合粉砕して混
濁液とし、この混濁液をAとする。
また別に、滑石微粉末49gを四塩化エチレン
(2Cc12,林純薬工業,試薬1級)2000c.c.中に入
れ、マグネチツクスターラで0.5時間撹拌混合し
て混濁液とし、この混濁液をBとする。この混濁
液Bを上記装置で撹拌しながら、混濁液Aを注入
して乳化分散させて、鉄化合物とモリブデン化合
物/滑石のエマルジヨンを作つた。この時滑石
は、A液の周囲を取りかこみ乳化剤としての役割
りを果たす。
次に、このエマルジヨンをガス温度160℃でデ
イスク径105φmmで3600rPmの条件で噴務乾燥造
粒した。この平均粒径は100μmの顆粒であり、
内部にFe2O3とMoO3を蔵して外表面が滑石にて
被覆されたものであつた。この顆粒粉末を1500
Kg/cm2の加圧力で13.5φ×1.35tmmと75φ×4.5tmm
の2種類の円盤を成形した。これを大気中900℃
で1時間仮焼してポリエチレングリコールを除去
して、水素雰囲気中の1300℃で1時間、露点30℃
の条件で焼結して、鉄とモリブデンを内蔵したフ
オルステライトとエンスタタイトを外皮面とする
組成の複合体が得られた。
以上の円盤品にて特性を調べ、比較品としてフ
オルステライトおよびエンスタタイトを調べ下記
に示した。
The present invention relates to a ceramic-metal composite material with improved thermal conductivity and a method for producing the same.More specifically, the fracture surface of the composite material is enlarged and microscopically shows that each inner core is made of iron or iron and molybdenum metal. The present invention relates to a composite material in which the inner and outer skin surfaces of each of the inner and outer skins are coated with a forsterite-enstatite-based film and bonded together, and the outer surface of the material is coated with a forsterite-enstatite-based film layer, and a method for producing the same. Forsterite and similar enstatite ceramics have long been available, and these ceramics have excellent electrical insulation properties and good metallization properties, and their sintering temperatures are as low as 1,200 to 1,400 degrees Celsius, making them ideal for electronic components. It is suitable as an insulating material. However, the thermal conductivity of these ceramics is 1/1 that of alumina or magnesia ceramics.
5 to 1/10, poor heat dissipation, thick film IC
There were major restrictions on its use as a substrate or resistance substrate. The present invention has been made to solve the above-mentioned problems, and its gist is based on a ceramic-metal composite material and a manufacturing method thereof as set forth in the claims. The present invention aims to improve thermal conductivity without impairing the electrical insulation properties of ceramics by obtaining a sintered body in which the inner core is a metal and the outer surface of the core is made of ceramics. Since there is not much difference in the coefficient of thermal expansion between tellite and iron, it is easy to combine the two, and by adjusting the mixing ratio of iron and molybdenum, which has a small coefficient of thermal expansion, the difference in coefficient with forsterite can be reduced. It is made smaller and more complex. Additionally, test results have shown that iron compounds or iron compounds and molybdenum compounds/talcum type emulsions are more effective than other types of solid emulsifiers for creating composite particles of ceramics and metals. In addition, it must be taken into account that the above metal compounds are reduced to metals at temperatures below the sintering temperature of ceramics, and that they are dispersed or dissolved in water, and the melting point of the metals must be above the sintering temperature of porcelain. This is the selected one. An enlarged microscopic view of the fractured surface of the composite material created using the above method shows that each inner core is made of iron metal or iron and molybdenum metal, and the outer skin surface of each inner core is covered with a forsterite-enstatite ceramic film. To briefly explain the formation mechanism, turbid liquid A, which is made by adding water and polyethylene glycol to an iron compound or a mixture of an iron compound and a molybdenum compound, is poured into turbid liquid B, which is made by mixing and dispersing talc in a non-aqueous solvent. When strongly stirred while stirring, the turbid liquid A becomes fine particles and is dispersed in the nonaqueous solvent. In this case, talc acts as an emulsifier to stably disperse the fine particles of the turbid liquid A to prevent them from aggregating with each other, and the talcum surrounds the fine particles of the turbid liquid A. When this emulsion is granulated in a spray dryer, granules are formed in which the inner core is made of an iron compound or an iron compound and a molybdenum compound, and the outer surface is made of talc. When this granule powder is pressure-molded and sintered in a non-oxidizing atmosphere, 3MgO, 4SiO 2 , H 2 O of talcum is converted into forsterite 2MgO,
SiO 2 and enstatite MgO/SiO 2 become glassy, while Fe 2 O 3 is reduced to Fe,
MoO 3 becomes Mo and the desired composite material is obtained. The fractured surface of this sintered body was observed with a scanning electron microscope, and the structure is shown in Fig. 1 in an enlarged microscopic view. It is a composite material that combines iron and molybdenum 2. The ceramic-metal composite material obtained by the present invention has a thermal conductivity of 0.10ca1/cm・at room temperature.
sec・℃, and the volume resistivity is 4×10 13 at room temperature.
Ω・cm, forstellite 0.012ca1/
Thermal conductivity can be greatly improved compared to cm・sec・℃ and 8×10 13 Ω・cm and enstatite's 0.006ca1/cm・sec・℃ and 3×10 14 Ω・cm.
Despite this, the volume resistivity was not low, making it a highly practical material. Examples will be described below, but the present invention is not limited thereto within the scope of the gist of the present invention. Example Ferric oxide (Fe 2 O 3 , Hayashi Pure Chemical Industries, Ltd., Reagent 1
450 g of molybdenum oxide (MoO 3 , Yoneyama Pharmaceutical Co., Ltd., reagent grade 1), 1400 c.c. of water, and 7 g of #4000 polyethylene glycol as a binder were mixed and ground in an alumina porcelain ball mill for 15 hours to form a turbid liquid. This turbid liquid is called A. Separately, 49 g of talc fine powder was placed in 2000 c.c. of ethylene tetrachloride (2Cc1 2 , Hayashi Pure Chemical Industries, reagent grade 1), stirred and mixed with a magnetic stirrer for 0.5 hours to form a turbid liquid, and this turbid liquid was Let it be B. While stirring this turbid liquid B using the above-mentioned apparatus, turbid liquid A was injected and emulsified and dispersed to prepare an emulsion of an iron compound and a molybdenum compound/talcum. At this time, the talcum surrounds the A liquid and acts as an emulsifier. Next, this emulsion was jet-dried and granulated under the conditions of a gas temperature of 160°C, a disk diameter of 105φmm, and 3600 rPm. This average particle size is granules of 100 μm,
It contained Fe 2 O 3 and MoO 3 inside, and its outer surface was covered with talc. 1500 of this granule powder
13.5φ×1.35tmm and 75φ×4.5tmm with pressure force of Kg/ cm2
Two types of discs were molded. This is heated to 900℃ in the atmosphere.
Calcinate for 1 hour at 1300℃ in a hydrogen atmosphere to remove polyethylene glycol, and heat to a dew point of 30℃.
By sintering under these conditions, a composite was obtained with a skin of forsterite and enstatite containing iron and molybdenum. The characteristics of the above disk products were investigated, and forsterite and enstatite were investigated as comparison products and are shown below.
【表】
上記、熱伝導度は三鬼エンジニアリング(株)製の
熱定数測定装置TLP―1000型、体積固有低抗は
タケダ理研(株)製のエレクトロメータTR―8651に
て測定した。
以上の実施例では粉末の加圧成形について記述
したが、他の1〜3種のバインダーを添加するこ
とにより、キヤステイングによるシート成形も可
能である。
以上、記述したように本発明の複合材料はマグ
ネシヤセラミツクスと同程度の熱伝導度であるた
めに、厚膜用IC基板をはじめ抵抗基板等の電子
部品用絶縁材や磁石撹拌子として使用出来る材料
である。[Table] The above thermal conductivity was measured using a thermal constant measuring device TLP-1000 manufactured by Miki Engineering Co., Ltd., and the volume specific resistance was measured using an electrometer TR-8651 manufactured by Takeda Riken Co., Ltd. Although the above embodiments described pressure molding of powder, sheet molding by casting is also possible by adding one to three other binders. As described above, the composite material of the present invention has a thermal conductivity comparable to that of magnesia ceramics, so it can be used as an insulating material for electronic components such as thick-film IC boards and resistance boards, and as a magnetic stirrer. It is the material.
第1図は破断面の拡大巨視的な構造を示したも
のである。
1……フオルステライト―エンスタタイト系セ
ラミツクの被膜層、2……鉄あるいは鉄とモリブ
デン。
FIG. 1 shows an enlarged macroscopic structure of the fracture surface. 1...Forsterite-enstatite ceramic coating layer, 2...Iron or iron and molybdenum.
Claims (1)
鉄金属あるいは鉄とモリブデン金属でありその
各々の内核外皮面がフオルステライト―エンスタ
タイト系セラミツク皮膜で被覆されて結合し、材
料の外表面がフオルステライト―エンスタタイト
系皮膜層よりなることを特徴とするセラミツクと
金属との複合材料。 2 鉄化合物あるいは鉄化合物とモリプデン化合
物との混合物に水とポリエチレングリコールを加
え混合粉砕しA混濁液とし、また別に水と相溶性
のない非水溶媒に、乳化剤として滑石を混合分散
させてB混濁液として、このB混濁液を撹拌しな
がら上記A混濁液を注入して乳化分散させ、鉄化
合物あるいは鉄化合物とモリブデン化合物/滑石
のエマルジヨンとして、これを噴霧乾燥機にて造
粒して、内核が鉄化合物あるいは鉄化合物とモリ
ブデン化合物とし、その外皮面が滑石よりなる顆
粒を製作し、この顆粒粉末を所定の形状に加圧成
形后、非酸化性雰囲気中の1200〜1400℃にて焼結
して、内核が鉄金属あるいは鉄金属とモリブデン
金属で、その外皮面がフオルステライト―エンス
タタイト系セラミツク皮膜で被覆されて結合し、
焼結体の外表面がフオルステライト―エンスタタ
イト系皮膜層よりなることを特徴とするセラミツ
クと金属との複合材料の製造法。 3 特許請求の範囲第2項記載の非水溶媒は、四
塩化エチレンであることを特徴とするセラミツク
と金属との複合材料の製造法。[Scope of Claims] 1 The fracture surface of the composite material is enlarged and microscopically shows that each inner core is made of iron metal or iron and molybdenum metal, and the outer skin surface of each inner core is covered with a forsterite-enstatite ceramic film. A composite material of ceramic and metal that is bonded together and whose outer surface consists of a forsterite-enstatite film layer. 2 Water and polyethylene glycol are added to an iron compound or a mixture of an iron compound and a molybdenum compound, mixed and ground to obtain a turbid solution A, and talcum is mixed and dispersed as an emulsifier in a non-aqueous solvent that is not compatible with water to obtain a turbid B. As a liquid, the above-mentioned turbid liquid A is poured into the turbid liquid B while stirring to emulsify and disperse it, and this is granulated in a spray dryer to form an emulsion of an iron compound or an iron compound and a molybdenum compound/talcum, and the inner core is formed. Granules are made of an iron compound or an iron compound and a molybdenum compound, and the outer surface is made of talcum. After the granules are press-formed into a predetermined shape, they are sintered at 1200 to 1400℃ in a non-oxidizing atmosphere. Then, the inner core is made of iron metal or iron metal and molybdenum metal, and the outer skin surface is covered with a forsterite-enstatite ceramic film and bonded,
A method for producing a composite material of ceramic and metal, characterized in that the outer surface of the sintered body is composed of a forsterite-enstatite film layer. 3. A method for producing a composite material of ceramic and metal, characterized in that the non-aqueous solvent according to claim 2 is ethylene tetrachloride.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56197087A JPS58100658A (en) | 1981-12-08 | 1981-12-08 | Ceramic-metal composite material and its manufacture |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56197087A JPS58100658A (en) | 1981-12-08 | 1981-12-08 | Ceramic-metal composite material and its manufacture |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58100658A JPS58100658A (en) | 1983-06-15 |
| JPS6155579B2 true JPS6155579B2 (en) | 1986-11-28 |
Family
ID=16368502
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56197087A Granted JPS58100658A (en) | 1981-12-08 | 1981-12-08 | Ceramic-metal composite material and its manufacture |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58100658A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01135996A (en) * | 1987-11-19 | 1989-05-29 | Bridgestone Corp | Liquid-tight proceeding retreating structure of cylindrical body |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6344423B2 (en) | 1998-02-26 | 2002-02-05 | Kabushiki Kaisha Ohara | High rigidity glass-ceramic substrate for a magnetic information storage medium |
| CN100387379C (en) * | 2005-12-22 | 2008-05-14 | 株洲钻石切削刀具股份有限公司 | Forming agent for cermet production |
-
1981
- 1981-12-08 JP JP56197087A patent/JPS58100658A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01135996A (en) * | 1987-11-19 | 1989-05-29 | Bridgestone Corp | Liquid-tight proceeding retreating structure of cylindrical body |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58100658A (en) | 1983-06-15 |
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