JPS5988337A - Glaze composition for ceramic substrate - Google Patents

Glaze composition for ceramic substrate

Info

Publication number
JPS5988337A
JPS5988337A JP19833482A JP19833482A JPS5988337A JP S5988337 A JPS5988337 A JP S5988337A JP 19833482 A JP19833482 A JP 19833482A JP 19833482 A JP19833482 A JP 19833482A JP S5988337 A JPS5988337 A JP S5988337A
Authority
JP
Japan
Prior art keywords
ceramic substrate
composition
mol
glaze
frit glass
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
Application number
JP19833482A
Other languages
Japanese (ja)
Other versions
JPS6343330B2 (en
Inventor
Shirohito Matsuyama
城仁 松山
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.)
NARUMI GIJUTSU KENKYUSHO KK
Original Assignee
NARUMI GIJUTSU KENKYUSHO KK
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 NARUMI GIJUTSU KENKYUSHO KK filed Critical NARUMI GIJUTSU KENKYUSHO KK
Priority to JP19833482A priority Critical patent/JPS5988337A/en
Publication of JPS5988337A publication Critical patent/JPS5988337A/en
Publication of JPS6343330B2 publication Critical patent/JPS6343330B2/ja
Granted legal-status Critical Current

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  • Glass Compositions (AREA)

Abstract

PURPOSE:To obtain a composition having high surface smoothness, >=750 deg.C yield point and high heat resistance without adding alkali and Pb by using a specified mol% each of SiO2, Al2O3, >=1 kind among CaO, SrO and BaO, and B2O3 as principal components. CONSTITUTION:This glaze composition for a ceramic substrate consists essentially of, by mole, 58-63% SiO2, 6-12% Al2O3, 20-28% >=1 kind among CaO, SrO and BaO, and 3-8% B2O3. Starting materials for the composition are well mixed, melted at 1,280-1,450 deg.C for 20-40min in a refractory crucible, and charged into water to form frit glass by rapid cooling. The frit glass is suspended in water, sprayed on a ceramic substrate, and calcined at 1,170-1,260 deg.C. The frit glass may be mixed with an org. binder and printed on the substrate.

Description

【発明の詳細な説明】 本発明は、セラミック基板に施釉されるグレーズ組成物
に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a glaze composition for glazing a ceramic substrate.

最近ファクシミリなどの電子機器などの開発に伴ない、
例えばり−−マルヘッドなどに用いるグレーズドセラミ
ック基板の需要が高まっている。かかるグレーズドセラ
ミック基板は良好な回路配線を得ることや、発熱体を均
一にっりることなどの要求からグレーズ面の表面平滑度
が良いことが望まれ、また、勿論電気絶縁性が高いこと
も望まれている。そして特にファクシミリのサーマルヘ
ッドにおいては、ファクシミリの印字スピードが益々高
速化されるに伴ない温度の急激な1胃および降下という
厳しい条件にさらされるようになってきたために、J−
記の特性のばかに高度な□耐熱性も要求されるJ、うに
なってきている。
With the recent development of electronic devices such as facsimiles,
For example, there is an increasing demand for glazed ceramic substrates used in multi-heads and the like. Such glazed ceramic substrates are desired to have good surface smoothness on the glazed surface due to requirements such as obtaining good circuit wiring and uniformly glazing the heating element, and of course also having high electrical insulation properties. desired. In particular, facsimile thermal heads have come to be exposed to severe conditions such as rapid temperature drops and rapid temperature drops as facsimile printing speeds have become increasingly faster.
In addition to the above characteristics, high heat resistance is also required.

ところで従来のグレーズドセラミック基板にJ3いては
、グレーズ表面の平滑性を保つ意味でアルカリと鉛を含
有している。そのため屈伏点が550〜610℃程度と
なり、又、多数回の反復使用により、アルカリと鉛の濃
縮が起り電気絶縁性が低下していた。アルカリと鉛を含
有するグレーズでも屈伏点を700’C以上に゛するこ
とができるが、その場合には平滑性が悪くなる。
By the way, the conventional glazed ceramic substrate J3 contains alkali and lead in order to maintain the smoothness of the glazed surface. As a result, the yield point was approximately 550 to 610°C, and due to repeated use many times, alkali and lead were concentrated, resulting in a decrease in electrical insulation. A glaze containing alkali and lead can also have a yield point of 700'C or higher, but in that case, the smoothness deteriorates.

本発明者は上記従来の欠点を改良するため、さきに、無
鉛、無アルカリで表面平滑性も良く、屈伏点も740℃
付近と^いグレーズ組成物をtut発したが、本発明に
おいてはそれをさらに改良し、アルカリと鉛を含有せず
に良好な表面平滑度を有し、しかも屈伏点が150℃以
上であり耐熱性が良好で、反復使用による電気絶縁性の
低下もないヒラミック基板用グレーズ和成物を提供する
ものである。Jなわら本発明の要旨は、S!0258〜
63モル%、AI  2036〜12モル%、CaOと
SrOとeaoの少なくとも1秤を20へ・28モル%
、 82033〜8tル%を主成分としてなることを特
徴どするセラミック基板用グレーズ組成物である。
In order to improve the above-mentioned conventional drawbacks, the present inventors first developed a product that is lead-free, alkali-free, has good surface smoothness, and has a yield point of 740°C.
In the present invention, we have developed a glaze composition that has a relatively low temperature, but in the present invention, it has been further improved to have a good surface smoothness without containing alkali and lead, and a heat-resistant glaze composition with a yield point of 150°C or higher. The object of the present invention is to provide a glaze composition for a Hiramic substrate which has good properties and whose electrical insulation properties do not deteriorate due to repeated use. The gist of the present invention is S! 0258~
63 mol%, AI 2036-12 mol%, at least one weight of CaO, SrO and eao to 20/28 mol%
, 82033 to 8 t% as a main component.

本発明において、Si 02はガラスを構成づる主成分
であり、その白が58モル%未満で他の酸化物が増加す
るとグレーズ面に揮発とピンホールが同時に起りやすく
なる。また、63モル%を越えると硬いグレーズとなっ
て中に発生する泡が抜けにくくなる。
In the present invention, Si 02 is the main component constituting the glass, and if its white content is less than 58 mol % and other oxides increase, volatilization and pinholes are likely to occur simultaneously on the glaze surface. Moreover, if it exceeds 63 mol%, it becomes a hard glaze, making it difficult for the bubbles generated therein to come out.

Al2O3は屈伏点を向上させ、かつアルカリ土類と共
存する場合に融剤としで働きグレーズを融かしやりくす
る。その量が6モル%未満では屈伏点が7506C以下
となるばかりでなく、ピンボールが操りがたくなる。1
2モル%を越えると1170〜1260℃の必要焼成温
度においてグレーズ表面が悪くなる。
Al2O3 improves the yield point and, when coexisting with alkaline earth metals, acts as a flux to help melt the glaze. If the amount is less than 6 mol%, not only will the yield point be 7506C or lower, but the pinball will become difficult to control. 1
If it exceeds 2 mol %, the glaze surface will deteriorate at the required firing temperature of 1170 to 1260°C.

本発明では、アルカリ土類としてCa O。In the present invention, CaO is used as the alkaline earth element.

Sr O,Ba Oのどれを用いても表向平滑度の良い
グレーズが得られることが判った。そして、これらの酸
化物の総量が28モル%を越えると屈伏点が750℃以
下となり、熱膨張係数が大きくなる。場合にJ、っては
熱膨張係数がアルミナ基板より人となって、焼成時にク
ラック(貫入)が入りやず、くなる。また、20モル%
未満では融解しにくくなり、乳白色を呈J−るか、未融
解のまま残り、所期の効果を奏しない。
It has been found that a glaze with good surface smoothness can be obtained using either Sr 2 O or Ba 2 O. If the total amount of these oxides exceeds 28 mol %, the yield point will be 750° C. or lower, and the thermal expansion coefficient will increase. In the case of J, the coefficient of thermal expansion is higher than that of the alumina substrate, and cracks (penetration) do not occur during firing. Also, 20 mol%
If it is less than that, it becomes difficult to melt and takes on a milky white color or remains unmelted, failing to produce the desired effect.

B203は強力な媒溶剤であるが、3モル%未満ではそ
の効果があられれず、融解しにくくなる。8モル%を越
えると融解力が大きく屈伏点を150℃から著しく下げ
てしまう。
B203 is a strong solvent, but if it is less than 3 mol %, its effect is lost and it becomes difficult to melt. If it exceeds 8 mol%, the melting power will be large and the yield point will be significantly lowered from 150°C.

本発明において、Zn O,MgO1ri 02は6モ
ル%までは添加してもグレーズの特性に全く影響を与え
ない。
In the present invention, ZnO and MgO1ri02 do not affect the properties of the glaze at all even when added up to 6 mol%.

また、使用原料から必然的に混入してくる種々の酸化物
は、0.2モル%までは不可避的不純物どして混入して
いても差支えない。
Further, various oxides inevitably mixed in from the raw materials used may be mixed as unavoidable impurities up to 0.2 mol %.

本発明では以上の組成によって、それぞれの特性が相俟
って、アルカリ、鉛を含有しないでも良Ofな表面平W
#度を右し、反復使用による電気絶縁性の低下もなく、
750℃以上の屈伏点を有する耐熱性の高いグレーズが
得られるのである。
In the present invention, due to the above-mentioned composition, each property is combined to provide a flat surface W that is good even without containing alkali or lead.
#The degree is right, and there is no deterioration of electrical insulation properties due to repeated use.
A highly heat-resistant glaze with a yield point of 750° C. or higher can be obtained.

本発明のグレーズをつくるためには、各組成原料は、酸
化物、水酸化物あるいは炭酸塩のいずれの形で用いでも
良いが、溶融し易いように微粉砕原料や化合物を使用し
た方が良い。これらの原料をよく混合し、耐火るつぼ中
で1280〜1450℃で20〜40分間溶融後、水中
に投入して急冷し、フリツI・ガラスを得る。
In order to make the glaze of the present invention, each component raw material may be used in the form of an oxide, hydroxide or carbonate, but it is better to use finely pulverized raw materials or compounds so that they can be easily melted. . These raw materials are thoroughly mixed, melted in a fireproof crucible at 1280 to 1450°C for 20 to 40 minutes, and then poured into water to be rapidly cooled to obtain Fritz I glass.

これを廿ラミック基板に施すには、水中に懸濁させ、ス
プレ一方式によってセラミック基板上に付着さLるか、
エチルセルローズの如き巻機バインダと混合し、印刷方
式によってセラミック基板上に印刷し、これを1170
〜1260℃で焼成Jればよい。
To apply this to a ceramic substrate, it can be suspended in water and applied to a ceramic substrate by spraying.
Mixed with a winding machine binder such as ethyl cellulose and printed on a ceramic substrate by a printing method, the 1170
It is sufficient to perform firing at ~1260°C.

本発明の対象となるセラミック基板として番よ、アルミ
ナ基板おにぴこれと同程麿の膨張係数(70〜90X 
1O−7)を有するセラミック基板が好適である。
As a ceramic substrate that is the subject of the present invention, an alumina substrate with an expansion coefficient as high as this (70 to 90X
1O-7) is preferred.

つぎに実施例について述べる。Next, examples will be described.

下記表に本発明の実施例N011〜N009と比較例(
従来品)の組成を示し、その試験結果を示す。
The table below shows examples N011 to N009 of the present invention and comparative examples (
The composition of conventional product) and its test results are shown below.

組               成        
(モル%)ZnO 618265 61813135 61813135 63625E1 58     12               2
7    361      10    24   
            562      6   
        23         5     
MTIO626101351“10z (j 62      6           13  1
0     Ei     ZnO62,69,54,
63,211,95,3特     性 NazOK2O ℃   平滑性   108回 800   良   クラックなし 790   〃 780   JI 760   I/ 780   〃 810   !! 780   〃 770   l! 760    、。
Composition
(mol%) ZnO 618265 61813135 61813135 63625E1 58 12 2
7 361 10 24
562 6
23 5
MTIO626101351"10z (j 62 6 13 1
0 Ei ZnO62,69,54,
63,211,95,3 Properties NazOK2O ℃ Smoothness 108 times 800 Good No cracks 790 〃 780 JI 760 I/ 780 〃 810! ! 780 〃 770 l! 760,.

2.1   0.7  670    〃上記表で明ら
かなとおり、本発明品はアルカリと鉛を含有せず所定の
グレーズ組成物である/Cめ、屈伏点が760〜800
℃と従来品のグレーズに比べ90〜140℃と高くなっ
ており、耐熱性が向上している。又、本発明品を71ク
シミリのり−−マルヘッドとして連続パルス試験を行な
っlcどころ、10Bパルス以上を過ぎてもグレーズに
クラックが発生せず、電気絶縁性が低下するようなこと
はなかった。さらに、本発明品の表面平滑性は良好で、
うねりを生ずるようなことがなく、複ttt、細密な回
路配線でも良好に設けることができる。
2.1 0.7 670 As is clear from the table above, the product of the present invention does not contain alkali or lead and is a prescribed glaze composition /C, with a yield point of 760-800
The temperature is 90 to 140°C, which is higher than that of conventional glazes, and the heat resistance is improved. Further, a continuous pulse test was carried out using the product of the present invention as a 71 comb glue head, and no cracks were generated in the glaze even after 10 B pulses or more, and there was no deterioration in electrical insulation. Furthermore, the surface smoothness of the product of the present invention is good;
It does not cause any waviness and can be satisfactorily installed even in multi-ttt and fine circuit wiring.

特許出願人 鳴海製陶株式会社 代理人  弁理士  小松秀岳Patent applicant: Narumi Seito Co., Ltd. Agent: Patent attorney: Hidetake Komatsu

Claims (1)

【特許請求の範囲】[Claims] l、  5i0258〜63モル%、△120!16〜
12モル%、CaOとSrOとBaOの少なくども1種
を20〜28モル%、B20s 3〜8モル%を主成分
どしてなることを特徴と覆るセラミック基板用グレーズ
組成物。
l, 5i0258~63 mol%, △120!16~
12 mol% of at least one of CaO, SrO and BaO as main components, 20 to 28 mol% of at least one of CaO, SrO and BaO, and 3 to 8 mol% of B20s as main components.
JP19833482A 1982-11-13 1982-11-13 Glaze composition for ceramic substrate Granted JPS5988337A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19833482A JPS5988337A (en) 1982-11-13 1982-11-13 Glaze composition for ceramic substrate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19833482A JPS5988337A (en) 1982-11-13 1982-11-13 Glaze composition for ceramic substrate

Publications (2)

Publication Number Publication Date
JPS5988337A true JPS5988337A (en) 1984-05-22
JPS6343330B2 JPS6343330B2 (en) 1988-08-30

Family

ID=16389379

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19833482A Granted JPS5988337A (en) 1982-11-13 1982-11-13 Glaze composition for ceramic substrate

Country Status (1)

Country Link
JP (1) JPS5988337A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20010092981A (en) * 2000-03-28 2001-10-27 김형순 tile glaze and its manufacturing method
JP2005330176A (en) * 2003-12-26 2005-12-02 Asahi Glass Co Ltd No-alkali glass and liquid crystal display panel
US8343617B2 (en) 2009-04-09 2013-01-01 Industrial Technology Research Institute Ceramic substrate

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3501322A (en) * 1967-08-16 1970-03-17 Corning Glass Works Glazed ceramic substrate for electronic microcircuits
JPS5292224A (en) * 1976-01-28 1977-08-03 Nippon Electric Glass Co Composite of glass for glazing
JPS5654253A (en) * 1979-10-11 1981-05-14 Ngk Spark Plug Co Ltd Glaze composition for alumina substrate
JPS57118077A (en) * 1981-01-06 1982-07-22 Central Glass Co Ltd Manufacture of glazed ceramic substrate
JPS5867091A (en) * 1981-10-19 1983-04-21 日本特殊陶業株式会社 Glazed ceramic board
JPS598638A (en) * 1982-07-06 1984-01-17 Ngk Spark Plug Co Ltd Glaze composition
JPS6124345A (en) * 1984-07-12 1986-02-03 Yaskawa Electric Mfg Co Ltd Signal output gate control system
JPS6159557A (en) * 1984-08-30 1986-03-27 Toshiba Corp Virtual memory controlling device
JPS6215493A (en) * 1985-07-15 1987-01-23 株式会社東芝 Spent fuel transport and storage vessel

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3501322A (en) * 1967-08-16 1970-03-17 Corning Glass Works Glazed ceramic substrate for electronic microcircuits
JPS5292224A (en) * 1976-01-28 1977-08-03 Nippon Electric Glass Co Composite of glass for glazing
JPS5654253A (en) * 1979-10-11 1981-05-14 Ngk Spark Plug Co Ltd Glaze composition for alumina substrate
JPS57118077A (en) * 1981-01-06 1982-07-22 Central Glass Co Ltd Manufacture of glazed ceramic substrate
JPS5867091A (en) * 1981-10-19 1983-04-21 日本特殊陶業株式会社 Glazed ceramic board
JPS598638A (en) * 1982-07-06 1984-01-17 Ngk Spark Plug Co Ltd Glaze composition
JPS6124345A (en) * 1984-07-12 1986-02-03 Yaskawa Electric Mfg Co Ltd Signal output gate control system
JPS6159557A (en) * 1984-08-30 1986-03-27 Toshiba Corp Virtual memory controlling device
JPS6215493A (en) * 1985-07-15 1987-01-23 株式会社東芝 Spent fuel transport and storage vessel

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20010092981A (en) * 2000-03-28 2001-10-27 김형순 tile glaze and its manufacturing method
JP2005330176A (en) * 2003-12-26 2005-12-02 Asahi Glass Co Ltd No-alkali glass and liquid crystal display panel
US8343617B2 (en) 2009-04-09 2013-01-01 Industrial Technology Research Institute Ceramic substrate

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Publication number Publication date
JPS6343330B2 (en) 1988-08-30

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