JPS5836948A - Alumina substrate - Google Patents

Alumina substrate

Info

Publication number
JPS5836948A
JPS5836948A JP13250981A JP13250981A JPS5836948A JP S5836948 A JPS5836948 A JP S5836948A JP 13250981 A JP13250981 A JP 13250981A JP 13250981 A JP13250981 A JP 13250981A JP S5836948 A JPS5836948 A JP S5836948A
Authority
JP
Japan
Prior art keywords
glass
alumina substrate
glass layer
cao
sum
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
JP13250981A
Other languages
Japanese (ja)
Inventor
Masaru Shinpo
新保 優
Kiyoshi Fukuda
潔 福田
Shozo Takeno
武野 尚三
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.)
Toshiba Corp
Original Assignee
Toshiba Corp
Tokyo Shibaura Electric 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 Toshiba Corp, Tokyo Shibaura Electric Co Ltd filed Critical Toshiba Corp
Priority to JP13250981A priority Critical patent/JPS5836948A/en
Publication of JPS5836948A publication Critical patent/JPS5836948A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C3/00Glass compositions
    • C03C3/04Glass compositions containing silica
    • C03C3/076Glass compositions containing silica with 40% to 90% silica, by weight
    • C03C3/089Glass compositions containing silica with 40% to 90% silica, by weight containing boron
    • C03C3/091Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium
    • C03C3/093Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium containing zinc or zirconium

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Electronic Switches (AREA)
  • Laminated Bodies (AREA)
  • Glass Compositions (AREA)

Abstract

PURPOSE:To give superior resistance to heat and pulses to an alumina substrate, by coatong the alumina substrate with a glass layer containing specified proportions of SiO2, Al2O3, BaO, CaO, SrO, B2O3, and ZrO2. CONSTITUTION:The surface of an alumina substrate is coated with a glass layer contg. by weight 48-55% SiO2, 8-15% Al2O3, 8-25% BaO, 5-15% CaO, 0- 15% SrO, 2-6% B2O3, and 1-5% ZrO2, and the total of these oxides amounting to >=95%, and the sum of SiO2 and Al2O3 amounting to 58-65%, and besides, the total of BaO, CaO, and SrO amounting to 20-35%. To coat this layer, this mixture is melted at 1,500-1,600 deg.C, crushed with a water-cooled roller, etc., further finely pulverized to 1-10mum average particle diameter, coated on the alumina substrate by screen printing, and heat treated at 1,200-1,300 deg.C.

Description

【発明の詳細な説明】 本発明はガラス層で被覆して◆るアル建す基板に係)、
特にサーマルヘッド等におけるアル建す基板の発熱抵抗
体保温のためIDガラス層の改良に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a substrate coated with a glass layer),
In particular, the present invention relates to improvements in ID glass layers for heat-insulating heat-generating resistors on substrates used in thermal heads and the like.

サーマルヘッドとは黴細な発熱抵抗体素子の上に感熱紙
t′走らせ、書暑込むべ1図形に対応した発熱抵抗体素
子に通電して発熱させ、感熱紙に記録を行うものである
。七〇発熱抵抗体部は、アル々す基板上を被うガラス層
、その上の発熱抵抗体層、さらにそO上の保護層から形
成された三層構造になっている。ζOアル建す基板上0
fラス層は、発熱抵抗体から基板への熱伝達のバリヤの
作用をもつものであ)、加えられる電力AJ&スに対応
して発熱抵抗体Oビーク温度と冷却速度を決定する重要
な役割管果している。従ってζOyツス層は10〜10
0μの範囲内で厚さが制御でき、均質で滑らかである必
要がある。tた結晶などの異物や泡、ピンホール、クラ
ッタなどは、そり上に形成される発熱抵抗体の形成の障
害に&るのでガラス層表面の性状は特に重要である。さ
らにこOfツス層は発熱抵抗体に直接接触しているため
に、ピーク温度s o o c’を越える大きな熱Δ羨
スを受けるのでこれに耐先なければならない、こO耐パ
ルス特性はサーマルヘッドプリンタの特性を左右する大
きな要因である。プリンタの高速化、大容量化と長寿命
化は世のすう勢であル、それに対応できるガラス層の開
発が特大れている。
A thermal head is a device in which thermal paper t' is run over a fine heating resistor element, and electricity is applied to the heating resistor element corresponding to the pattern to be written to generate heat, thereby recording on the thermal paper. The heating resistor part has a three-layer structure consisting of a glass layer covering the glass substrate, a heating resistor layer on top of the glass layer, and a protective layer on top of the glass layer. ζO Al construction board 0
The f-las layer acts as a barrier for heat transfer from the heating resistor to the board), and plays an important role in determining the O peak temperature and cooling rate of the heating resistor in response to the applied electric power. I am accomplishing it. Therefore, the ζOy tus layer is 10 to 10
The thickness must be controllable within the range of 0μ, and it must be homogeneous and smooth. The properties of the surface of the glass layer are particularly important because foreign substances such as crystals, bubbles, pinholes, clutter, etc. can hinder the formation of the heating resistor formed on the warp. Furthermore, since this OfTs layer is in direct contact with the heating resistor, it is subjected to a large heat Δx exceeding the peak temperature s o o c', so it must be able to withstand this. This is a major factor that affects the characteristics of head printers. Printers are becoming faster, have larger capacities, and have longer lifespans, and the development of glass layers that can accommodate these trends is at an all-time high.

さらに発熱抵抗体に通電される際熱せられたガラス層に
も電界がかか、るためアルカリイオンなどが存在すると
電気分解゛が起)、劣化するため、無アルカリのガラス
が必要である。
Furthermore, when the heating resistor is energized, an electric field is also applied to the heated glass layer, which causes electrolysis and deterioration if alkali ions are present, so alkali-free glass is required.

アルミナ基板用ガラスとしては従来810.−B、Os
−PbO−ムL、0.系、8102−ムz2os−pb
o−RO系(R:アルカリ土類)、StO,−ム1,0
s−R’20 (R’ :アルカリ)系、819.−ム
t、O,−B、O,−RO系などが知られているが、サ
ーマルヘッド用基板のガラスとしての見地からは充分な
特性のものがなかった。
The conventional glass for alumina substrates is 810. -B, Os
-PbO-muL, 0. system, 8102-muz2os-pb
o-RO system (R: alkaline earth), StO,-mu1,0
s-R'20 (R': alkali) system, 819. -Mut, O, -B, O, -RO systems are known, but none have sufficient characteristics from the viewpoint of glass for a substrate for a thermal head.

本発明の目的は均質かつ滑らかな表面性状が得られ、耐
熱性がありてサーマルヘッド用として使用したとき優れ
た耐パルス性が得られるガラス層t%つアル電す基板を
提供するにある。
It is an object of the present invention to provide a substrate having a glass layer of t%, which has a homogeneous and smooth surface, is heat resistant, and has excellent pulse resistance when used for a thermal head.

本発明におけるガラス層は81O□−ム!、O,−RO
−B、0.系に属する。この系自体は全知であるが、一
般に耐熱性を増そうとすると熱膨張係数の低下と失透性
をもたらすため、耐パルス特性の見地から充分な特性の
tのは知られてなかった。
The glass layer in the present invention is 81O□-mu! ,O,-RO
-B, 0. belongs to the system. Although this system itself is well known, in general, an attempt to increase heat resistance results in a decrease in the coefficient of thermal expansion and devitrification, so it has not been known that t has sufficient characteristics from the standpoint of pulse resistance characteristics.

そζでこの系を上記見地から見直してサーマルヘッド用
アル電す基板のガラス層として優れた組成域を見出した
。即ち本発明に係るアル建す基板のガラス層は、重量比
で810.48〜55−1Aj、0.8〜1511G、
BaO8〜25 lll5 CaO3〜151G、Br
OO〜15 %、1120B !! 〜6 * %Zr
O21〜5参を含みこれらの酸化物の総和が95−以上
であ)、かつ810.とムt、0□の和が58〜455
 * s BaO* CaOおよび8rO(D和が20
〜35−の範8にあることtq#黴とする・ 以下その組成限定O理由を説明する・サーマルヘッド用
として良好な特性會与えるためにはまず第1K%810
.とムt、0.0濃度が重要である。
Therefore, we reviewed this system from the above viewpoint and found a composition range that would be excellent as a glass layer for an aluminum substrate for a thermal head. That is, the glass layer of the aluminum substrate according to the present invention has a weight ratio of 810.48 to 55-1 Aj, 0.8 to 1511 G,
BaO8~25 lll5 CaO3~151G, Br
OO~15%, 1120B! ! ~6 *%Zr
containing 021 to 5, and the sum of these oxides is 95 or more), and 810. The sum of t and 0□ is 58 to 455
*s BaO* CaO and 8rO (D sum is 20
The reason for the composition limitation will be explained below.In order to provide good characteristics for thermal heads, the first K%810
.. and 0.0 concentration is important.

図はたて軸にムt20.濃度、横軸KSiO,の濃度管
の和が5・8−を示している。これらのlaK満たない
図の下方の組成は耐パルス特性が悪くなる。
The figure is on the vertical axis. The sum of the concentration tubes of the horizontal axis KSiO indicates 5.8-. Compositions in the lower part of the diagram below laK have poor pulse resistance.

これは恐らくガラスの耐熱性が不充分なためと考えられ
る。またムB線はw、o、 15 % %ムF線は81
0.48 %を表わしている。この範囲をはずれると、
ガラスが失透し易くな)、平滑なガラス面が得られなく
なる。次に:BC線は810゜とm、osO和が65−
1CDI#1810.#551gを示す。この範囲をは
ずれると、ガラスの流動、性が不良にな)、ピンホール
や膜の厚さむらを生じ易くなる。
This is probably due to the insufficient heat resistance of glass. Also, the mu B line is w, o, 15%, and the mu F line is 81
It represents 0.48%. Outside this range,
The glass tends to devitrify), making it impossible to obtain a smooth glass surface. Next: BC line is 810° and m, osO sum is 65-
1CDI#1810. #551g is shown. If it is out of this range, the flow and properties of the glass will be poor, and pinholes and uneven film thickness will likely occur.

全体に占めるアルカリ土類酸化物(RO)も重要である
。総和が35−を越えるとfラスO耐熱性が減じ、耐パ
ルス特性が劣化する。一方アルミナ基板と良好な整合性
を得るには、ガラスの熱膨張係数が52〜65 x 1
0−’/’Cの範囲にあ。
The proportion of alkaline earth oxides (RO) in the total is also important. If the total exceeds 35-, the f-las-O heat resistance will decrease and the pulse resistance will deteriorate. On the other hand, to obtain good compatibility with the alumina substrate, the coefficient of thermal expansion of the glass should be 52 to 65 x 1
It is in the range of 0-'/'C.

る必要があるが、ROの総和が20−未満では膨張係数
がこの範囲以下にな夛、ガラス層にフッツタが入シ1く
なる。ROとしての成分の中でCaOとBaOの濃度が
特に重要である。 CaOは熱膨張係数を増加させ、上
記範囲内に調整するために必須であり、最低S−以上必
要である力111511を越えるとガラスが失透性にな
)、嵐好チ以上必要であるがRO全全体占める割合−工
大、きくなl)、2511t−越えると耐パルス特性を
劣化させるこ去なく、熱膨張係数を上記範囲内に調整す
ることができなくなる。8rOは両者の中間的表作用を
示し、18gIIt−越えない範囲で加えれば、!ラス
O流動性が改良され−る。
However, if the sum of RO is less than 20, the coefficient of expansion will fall below this range, and the glass layer will have fuzz. Among the components as RO, the concentrations of CaO and BaO are particularly important. CaO is essential for increasing the coefficient of thermal expansion and adjusting it within the above range, and the glass becomes devitrified if the force exceeds the minimum force of 111511), but it is necessary to If the ratio of RO to the entire total exceeds 2511t, the pulse resistance characteristics will deteriorate and the thermal expansion coefficient cannot be adjusted within the above range. 8rO shows an intermediate surface effect between the two, and if added within a range not exceeding 18gIIt-! The lath O fluidity is improved.

以上のような組成範囲で限定されるガラスは−tの耐パ
ルス特性、基板との熱的整合性、流動性が得られるが、
基板とのぬれ性が充分で表く、またガラスの溶解温度も
1600Ct−越え、未溶解物を残し易い、これらの欠
点金改良するため[B20.とZ rOBが必須になる
@ B、O,は基板とガラスのぬれ性を良くし、溶解温
度を下げ、ガラスを均質化するために必要で2ts以上
でその効果が明らかになるが6−″を越えると耐熱性が
低くな〕、耐パルス特性を低下させる。一方Zr O2
はガラスの溶解温度を下げ、均質柱管向上させる上に耐
パルス特性も向上させる成分であり、19b以上でその
作用が顕著になるが、5−を越えるとガラスが失透性に
なシ好ましくない。
Glasses limited to the above composition range can provide -t pulse resistance, thermal compatibility with the substrate, and fluidity, but
In order to improve these drawbacks [B20. and Z rOB are essential @ B, O, are necessary to improve the wettability of the substrate and glass, lower the melting temperature, and homogenize the glass, and their effect becomes obvious at 2ts or more, but 6-" If the ZrO2
is a component that lowers the melting temperature of the glass, improves the homogeneity of the columnar tube, and also improves the pulse resistance properties, and its effect becomes noticeable at 19b or higher, but it is preferable that the glass becomes devitrified when it exceeds 5-. do not have.

以上のような基本組成に5−未満の範囲内でAg2O3
やsb、o、などの消泡剤p Coo p NIOeM
nOなどの着色剤g La201 e pbo # k
hlo tTi205sv205などのフラックスなど
を加えることができる。
Ag2O3 within the range of less than 5 to the above basic composition
Antifoaming agents such as , sb, o, etc. p Coo p NIOeM
Colorants such as nO g La201 e pbo #k
A flux such as hlotTi205sv205 can be added.

このようなガラスは、まず、常法に従りて各成分原料、
たとえば珪砂、水酸化ア4ルixウム、ホウ酸、炭酸バ
リウム、炭酸カルシウム、ジルコンなどの所要の組成に
従がって配合°シ、白金ルツがなどで1500〜160
0℃で溶融する0次いでこ0@@1ラスを水砕あるiは
水冷ローラなfラス粉末化すれに良i、アル11基板へ
OIk布紘スタリーン印刷が適轟である・すなわち、こ
れらOダツス看末を粘結剤としてエチルセル■−xなど
を會む、α−テレビノールなどO溶媒と混合してペース
)状とし、履的とするΔターンに印刷し九後ガラスが軟
化流動する温度、通常1200〜1300t:で焼成す
る。
To make such glass, first, each component raw material,
For example, silica sand, aluminum hydroxide, boric acid, barium carbonate, calcium carbonate, zircon, etc. are mixed according to the required composition, and platinum is used at 1500 to 160%.
0 which melts at 0℃, then this is good for turning the lath into powder using a water-cooled roller. The end of the glass is mixed with ethyl cell ■-x etc. as a binder, and mixed with an O solvent such as α-terewinol to form a paste), and printed on the target Δ turn at a temperature at which the glass softens and flows. , usually 1200 to 1300 tons.

〔実施例〕〔Example〕

810、などを下表に示す組成比(重量−)flc選び
、各成分原料を調音してパッチを作成し、白金ルツー(
SOO・、・、容量)で駿素一部市ガス炉を用いて1!
$00〜1600′cの温度で3時間溶解しえ、均質化
し九ガス融体を水冷嚢−ツ関で、冷却、薄片化し、畜も
Kが一ルζルで1日肴砕しガラス粉とし九・得られえガ
ラスの190℃〜800℃間の平均熱膨張係数を岡じ表
に示し九atたこれらのガラスはいずれも層状温度が7
50℃以上であった。
810, etc. in the composition ratio (weight -) flc shown in the table below, tune each component raw material to create a patch, and platinum Lutsu (
SOO・・・・capacity) using a Sunso gas furnace 1!
It can be melted for 3 hours at a temperature of $00 to 1600'C, homogenized, and the molten gas is cooled and sliced in a water-cooled bag-tube, and crushed for one day in a glass powder. The average coefficient of thermal expansion of the resulting glasses between 190°C and 800°C is shown in the table below. All of these glasses have a layer temperature of 7.
The temperature was 50°C or higher.

これらのガラス粉(325メッシ1通過)7゜に対し、
α−テレビオネール3−エチル竜ルーーズ溶液30の割
合で混合し、さらにこれを?−ルンルで2日微粉砕して
ガラスペーストを得た。
For these glass powders (325 mesh 1 passage) 7°,
Mix 30 parts of α-Televisionaire 3-Ethyl Loose solution, and then add ? - A glass paste was obtained by pulverizing for 2 days in Runlu.

25X25X2■のアル建す基板を用意し、上記ガラス
ペーストを幅10■のり一ン状に印刷し、1300℃で
15分焼成した。、fラス層の厚さは約30μになるよ
う調節した。内眼による外観検査ではいずれも良好であ
り、平滑度も±22μ内に収まっていた。次にこの上に
脅化タンタルをスバ、タリンダで1μの厚さに蒸着し、
苛性ソーダー過酸化水素のエツチング液を用い、幅10
0声、長さ600μの抵抗体/4ターンを形成さ・せた
、次に導・電性塗料をスクリーン印刷で塗布、焼成して
配線を形成させ、さらに抵抗素子の上に81021−蒸
着して保験膜とした。このテスト用素子に素子のピーク
温度が500℃になるよう調節した電力パルスk 10
 ms’尚シ1回の割合で10回通電し、その後の抵抗
値の変動を測電した。抵抗変動率5−以内が目標である
が、いずれの試料も高々3vI以内0変動率であった。
A 25 x 25 x 2 inch aluminum substrate was prepared, the glass paste was printed in a line shape with a width of 10 square meters, and baked at 1300°C for 15 minutes. The thickness of the f lath layer was adjusted to about 30μ. Visual inspection using the inner eye showed that all the pieces were good, and the smoothness was within ±22μ. Next, threatening tantalum was deposited on top of this to a thickness of 1μ using Suba and Talinda.
Width 10 using caustic soda hydrogen peroxide etching solution.
A resistor/4 turns with a length of 600μ and 0 voice was formed. Next, a conductive/electrical paint was applied by screen printing and baked to form wiring, and then 81021-81021 was vapor-deposited on the resistance element. It was used as a test membrane. A power pulse k 10 was applied to this test device, which was adjusted so that the peak temperature of the device was 500°C.
Current was applied 10 times at a rate of 1 time for ms', and the fluctuation in resistance value thereafter was measured. Although the target was a resistance variation rate of 5- or less, all samples had a resistance variation rate of 0 within 3vI at most.

尚、市販のグレーズドアル擢す(ガラスはホウケイ酸鉛
系)基板で同様な電力Δルス″印加を行表−)良が%l
X10’回のパルスで抵抗変動率が10−を越えた。
In addition, the same power ΔRus'' was applied to a commercially available glazed glass (lead borosilicate glass) substrate.
The resistance fluctuation rate exceeded 10- after X10' pulses.

【図面の簡単な説明】[Brief explanation of the drawing]

図は本発明におけるガラスの810.とム1,0.の濃
度関係を示す。
The figure shows 810. of glass in the present invention. Tomu1,0. shows the concentration relationship of

Claims (3)

【特許請求の範囲】[Claims] (1)  ガラス層で表面を被覆してなるアル建す基板
において、前記ガラス層は、重量比で1110゜48〜
551L At、0.8〜I S 91G、l1m08
〜25チ、CaO3〜1 !SIs% 8rOO−15
%、B、0゜2〜611% Zr0t 1〜5−’を含
み、これらの酸化物の総和が95−以上であシ、かつ8
10 とAA20.の和が58〜65−1B20 + 
CaOe BrOの和が20〜35%の範囲KToるこ
とt−%徴とするアル建す基板。
(1) In an aluminum substrate whose surface is coated with a glass layer, the glass layer has a weight ratio of 1110°48 to
551L At, 0.8~IS 91G, l1m08
~25chi, CaO3~1! SIs% 8rOO-15
%, B, 0°2 to 611% Zr0t 1 to 5-', the sum of these oxides is 95- or more, and 8
10 and AA20. The sum is 58~65-1B20 +
A substrate on which the sum of CaOe and BrO is in the range of 20 to 35% KTo or t-%.
(2)  ガラス層は、その上に形成される発熱抵抗体
の保温用である特許請求の範囲第1項記載のアルミナ基
板。
(2) The alumina substrate according to claim 1, wherein the glass layer is for keeping a heating resistor formed thereon warm.
(3)  ガラス層は、印刷法によル基板表面の所定領
域を被覆するように形成されるものである特許請求の範
囲第1現記゛載のアル電す基板。
(3) The aluminum substrate according to claim 1, wherein the glass layer is formed by a printing method so as to cover a predetermined area of the surface of the glass substrate.
JP13250981A 1981-08-24 1981-08-24 Alumina substrate Pending JPS5836948A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13250981A JPS5836948A (en) 1981-08-24 1981-08-24 Alumina substrate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13250981A JPS5836948A (en) 1981-08-24 1981-08-24 Alumina substrate

Publications (1)

Publication Number Publication Date
JPS5836948A true JPS5836948A (en) 1983-03-04

Family

ID=15083007

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13250981A Pending JPS5836948A (en) 1981-08-24 1981-08-24 Alumina substrate

Country Status (1)

Country Link
JP (1) JPS5836948A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61136937A (en) * 1984-12-04 1986-06-24 Asahi Glass Co Ltd Glass composition
JPS62104772A (en) * 1985-10-31 1987-05-15 Mitsubishi Electric Corp Thick-film thermal head
US4689270A (en) * 1984-07-20 1987-08-25 W. C. Heraeus Gmbh Composite substrate for printed circuits and printed circuit-substrate combination
FR2649296A1 (en) * 1989-07-06 1991-01-11 House Food Industrial Co PROCESS FOR PREPARING A PASTE CONTAINING FOOD AND PROCESS FOR PREPARING PASTE
JPH0380126A (en) * 1989-08-22 1991-04-04 Yamamura Glass Co Ltd Glaze composition
KR101039007B1 (en) 2008-07-28 2011-06-03 순천대학교 산학협력단 Aluminum hydroxide Particle Improving for Fire-retardant and Production Method Thereof

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4689270A (en) * 1984-07-20 1987-08-25 W. C. Heraeus Gmbh Composite substrate for printed circuits and printed circuit-substrate combination
JPS61136937A (en) * 1984-12-04 1986-06-24 Asahi Glass Co Ltd Glass composition
JPS62104772A (en) * 1985-10-31 1987-05-15 Mitsubishi Electric Corp Thick-film thermal head
FR2649296A1 (en) * 1989-07-06 1991-01-11 House Food Industrial Co PROCESS FOR PREPARING A PASTE CONTAINING FOOD AND PROCESS FOR PREPARING PASTE
JPH0380126A (en) * 1989-08-22 1991-04-04 Yamamura Glass Co Ltd Glaze composition
KR101039007B1 (en) 2008-07-28 2011-06-03 순천대학교 산학협력단 Aluminum hydroxide Particle Improving for Fire-retardant and Production Method Thereof

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