GB2107302A - Air-fireable thick film inks - Google Patents
Air-fireable thick film inks Download PDFInfo
- Publication number
- GB2107302A GB2107302A GB08219147A GB8219147A GB2107302A GB 2107302 A GB2107302 A GB 2107302A GB 08219147 A GB08219147 A GB 08219147A GB 8219147 A GB8219147 A GB 8219147A GB 2107302 A GB2107302 A GB 2107302A
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Classifications
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K13/00—Apparatus or processes specially adapted for manufacturing or adjusting assemblages of electric components
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/09—Use of materials for the conductive, e.g. metallic pattern
- H05K1/092—Dispersed materials, e.g. conductive pastes or inks
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/52—Electrically conductive inks
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/14—Conductive material dispersed in non-conductive inorganic material
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/14—Conductive material dispersed in non-conductive inorganic material
- H01B1/16—Conductive material dispersed in non-conductive inorganic material the conductive material comprising metals or alloys
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01C—RESISTORS
- H01C17/00—Apparatus or processes specially adapted for manufacturing resistors
- H01C17/06—Apparatus or processes specially adapted for manufacturing resistors adapted for coating resistive material on a base
- H01C17/065—Apparatus or processes specially adapted for manufacturing resistors adapted for coating resistive material on a base by thick film techniques, e.g. serigraphy
- H01C17/06506—Precursor compositions therefor, e.g. pastes, inks, glass frits
- H01C17/06513—Precursor compositions therefor, e.g. pastes, inks, glass frits characterised by the resistive component
- H01C17/06533—Precursor compositions therefor, e.g. pastes, inks, glass frits characterised by the resistive component composed of oxides
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01C—RESISTORS
- H01C17/00—Apparatus or processes specially adapted for manufacturing resistors
- H01C17/06—Apparatus or processes specially adapted for manufacturing resistors adapted for coating resistive material on a base
- H01C17/065—Apparatus or processes specially adapted for manufacturing resistors adapted for coating resistive material on a base by thick film techniques, e.g. serigraphy
- H01C17/06506—Precursor compositions therefor, e.g. pastes, inks, glass frits
- H01C17/06573—Precursor compositions therefor, e.g. pastes, inks, glass frits characterised by the permanent binder
- H01C17/0658—Precursor compositions therefor, e.g. pastes, inks, glass frits characterised by the permanent binder composed of inorganic material
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Dispersion Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Inorganic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Parts Printed On Printed Circuit Boards (AREA)
- Glass Compositions (AREA)
- Conductive Materials (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Non-Adjustable Resistors (AREA)
- Insulated Metal Substrates For Printed Circuits (AREA)
- Paints Or Removers (AREA)
Abstract
Improved air-fireable resistor and conductor inks useful in constructing multilayer integrated circuits on porcelain-coated metal substrates are provided. The subject inks comprise a barium calcium borosilicate glass frit, a suitable organic vehicle, and a functional component, such as ruthenium dioxide in the resistor inks and one or more precious metals plus bismuth oxide in the conductor inks, The glass comprises 40-55% by weight of barium oxide, 10-15% by weight of calcium oxide, 14-25% by weight of boron trioxide and 13-25% by weight of silicon dioxide.
Description
SPECIFICATION
Air-fireable thick film inks
This invention pertains to air-fireable thick film resistor and conductor inks and their use in multilayer electrical circuit structures on porcelain-coated metal substrates.
The use of specialized ink formulations to form thick films having various functions on suitable substrates in the construction of multilayer integrated circuit structures is well known in the art. Such technology is of increasing interest in the fabrication of very dense multilayer circuit patterns on various substrates for a wide variety of applications in the electronics industry.
Significantly improved substrates for the fabrication of such circuits are disclosed and claimed in
Hang et al., U.S. Patent 4,256,796, issued March 17, 1981, the disclosure of which is incorporated herein by reference. The Hang at al substrates are metal coated with an improved porcelain comprised of a mixture, based on its oxide content, of magnesium oxide (MgO) or mixtures of magnesium oxide and certain other oxides, barium oxide (BaO), boron trioxide (8203) and silicon dioxide (SiO2). The preferred metal is steel, particularly low carbon steel, which may be coated with various other metals such as, for example, copper. The porcelain compositions are applied to the metal core and fired to provide a partially devitrifled porcelain coating on the metal core.The coating has a very low viscosity at its initial fusion point and then almost instantaneously obtains a high viscosity due to devitrification.
The fired coatings, which are preferred for hybrid circuit applications, have a deformation temperature of at least 7000C and a high coefficient of thermal expansion of at least about 1 Ox 10-7/OC.
While the porcelain-coated metal substrates of Hang et al represent a significant improvement over previously known substrate materials, they are disadvantageous only in being incompatible or poorly compatible with commercially available thick-film inks. Air-fireable conductor and resistor inks compatible with the Hang at al substrates are provided in accordance with this invention.
Improved air-fireable inks provided in accordance with this invention comprise a barium calcium borosilicate glass, a suitable organic vehicle and a functional component. The functional component in the resistor inks Is ruthenium dioxide and in the conductor inks a precious metal in combination with bismuth oxide to improve solderability.
In accordance with this invention, there are provided air-fireable resistor and conductor inks of high reliability useful in forming thick-film circuits on porcelain metal circuit boards. The inks of this invention are particularly compatible with the Hang et al circuit boards, with each other, and with airfireable inks of other functions specifically formulated for the Hang et al boards. The economic advantage of producing electronic circuits wherein all inks are fireable in air as opposed to an inert atmosphere such as nitrogen is readily apparent to those skilled in the art.
The novel inks of this invention are comprised of a barium calcium borosilicate glass, a suitable organic vehicle, and one or more functional components. In the resistor inks, the functional component is ruthenium dioxide and, if desired, a temperature coefficient of resistance (TCR) modifier. In the conductor inks, the functional component is one or more precious metals and, as a soldering enhancer, bismuth oxide.
The glass frit of the novel inks of this invention is a barium calcium borosilicate glass consisting of, on a weight basis:
a) from about 40 to about 55 percent of barium oxide;
b) from about 10 to about 15 percent of calcium oxide;
c) from about 14 to about 25 percent of boron trioxide; and
d) from about 13 to about 23 percent of silicon dioxide.
The glass frit comprises from about 1 to about 80 percent by weight of the novel air-fireabie inks of this invention. The subject resistor inks preferably contain from about 25 to about 80 percent by weight of the glass frit with from about 50 to about 75 percent, by weight, being particularly preferred,
The subject conductor inks contain from about 1 to about 15 percent by weight of the glass frit with from about 1 to about 7 percent by weight being particularly preferred.
A preferred glass frit for the resistor inks of this invention consists of, on a weight basis, about 52 percent of barium oxide; about 12 percent of calcium oxide; about 16 percent of boron trioxide; and about 20 percent of silicon dioxide. A preferred glass frit for the subject conductor inks consists of, on a weight basis, about 52 percent of barium oxide, about 12 percent of calcium oxide, about 19 percent of boron trioxide, and about 17 percent of silicon dioxide.
The functional component, i.e. ruthenium dioxide or precious metal, of the subject air-fireable inks is present in from about 2 to about 90 percent by weight. The subject resistor inks contain from about 2 to about 60 percent, preferably about 5 to about 25 percent, by weight of ruthenium dioxide. The ruthenium dioxide of the subject resistor inks should be of high purity and preferably have a particle size range of from about 0.05 to about 0.2 micrometer.
The subject air-fireable resistor inks may also contain up to about 10 percent by weight of a conventional TCR modifier such as, for example, manganese dioxide, cadmium oxide, cuprous oxide, and the like.
The term precious metal as utilized in this invention indicates one or more art-recognized metals such as for example, gold, silver, platinum, palladium, rhodium, and the like. Combinations of the metals conventionally utilized in conductor inks such as, for example, silver/platinum, gold/platinum, silver/platinum/palladium, and the like are contemplated. All are utilized in pure form with the exception of rhodium which may also be utilized in the form of commercially available resinates. The precious metal comprises from about 60 to about 90 percent, preferably from about 70 to about 85 percent by weight, of the subject conductor inks.
The conductor inks of this invention contain, as a solderability enhancer, from about 1 to about 1 5 percent, preferably from about 1 to about 7 percent by weight of bismuth oxide, which may be present either as an additional powder component or as part of the glass frit. The bismuth oxide and the glass frit are preferably present in the subject conductor inks in a weight ratio of from about 1:3 to 3:1, most preferably in equal quantities.
The subject conductor inks optionally contain a small quantity, i.e., up to about 1 percent by weight, of a suitable oxidizing agent. The function of this additive is to provide a source of oxygen and oxidizing vapors as an aid in removing the organic vehicle during firing. A preferred oxidizing agent is bismuth nitrate pentahydrate which is effective over a broad temperature range in contrast to oxidizing agents which decompose at a specific temperature causing an undesirable abrupt release of gas.
The organic vehicles of the subject inks are binders such as, for example, cellulose derivatives, particularly ethyl cellulose, synthetic resins such as polyacrylates or methacrylates, polyesters, polyolefins, and the like. In general, conventional vehicles utilized in inks of the type described herein may be used in the subject inks. Preferred commercially available vehicles include, for example, pure liquid polybutenes available as Amoco H-25, Amoco H-50 and Amoco L-1 00 from Amoco Chemicals
Corporation, poly n-butylmethacrylate available from E. I. duPont deNemours and Co., and the like.
The above resins may be utilized individually or in any combination of two or more. A suitable viscosity modifier can be added to the resin material if desired. These modifiers can be solvents such as those conventionally used in similar ink compositions, e.g., pine oil, terpineol, butyl carbitol acetate, an ester alcohol available from Texas Eastman Company under the trademarkTexanol and the like, or solid materials such as, for example, a castor oil derivative available from N. L. Industries under the trademark Thixatrol. The organic vehicle comprises from about 8 to about 35 percent, by weight of the inks of this invention. The subject resistor inks preferably contain from about 20 to about 30 percent, by weight, of the vehicle.The subject conductor inks preferably contain from about 10 to about 25 percent, by weight, of the organic vehicle.
The improved air-fireable inks of this invention are applied to a porcelain-coated metal board such as described by Hang at al by conventional means, i.e., screen, printing, brushing, spraying, and the like, with screen printing being preferred. The coating is then dried in air at 1 00o#1 250 C, for about 1 5 minutes. The resulting film is then fired in air at peak temperatures of from 8500--9500C for from 4 to 10 minutes. The value of the resistor films can be adjusted by conventional means such as laser trimming or air abrasive trimming.
In addition to the superior compatibility with the Hang et al substrates and inks formulated therefor, films formed from the resistor inks of this invention have demonstrated very good TCR values,
laser trimmability, current noise level, and stability to thermal'shock, solder dipping, thermal storage, power loading and humidity. Films formed from the subject conductor inks have shown excellent conductivity, solderability, solder leach resistance, wire bondability and resistance to long term exposure to high humidity.
The following Examples further illustrate this invention, it being understood that the invention is in no way intended to be limited to the details described therein. In the Examples, all parts and percentages are on a weight basis and all temperatures are in degrees Celsius, unless otherwise stated.
Example 1
A gold conductor ink was prepared from the following formulation:
Ingredient Percent
Gold powder 83,33 Glass frit 1.04
Bismuth oxide 1.04
Bismuth nitrate pentahydrate 0.70
Organic vehicle 13.89
The glass frit had the following composition with percents in parenthesis: BaO (51.32); CaO (12.51); B203 (19.42); and siO2 (16.75). The organic vehicle comprised, on a percent of the final ink: ethylceliulose (0.58); terpineol (7.90); butyl carbinol acetate (3#23); Texanol (1.84); and Thixatrol (0.34).
Solutions of ethyl cellulose and Thixatrol in the liquid constituents of the vehicle were initially
prepared. The vehicle was combined and initially mixed by hand with the combined powder
ingredients. The ink was then mixed in a 3 roll mill with shearing to obtain a smooth paste suitable for screen printing. Additional vehicle was added to replace loss during mixing and to assure proper rheology.
The ink was printed on a porcelain-coated steel substrate of the type disclosed by Hang et al using a 325 mesh stainless steel screen, to a 1.0 mil emulsion thickness. The ink was air dried at 125C for 10 minutes and then fired in air in a belt furnace at a peak temperature of 9000 for 4 to 6 minutes at peak temperature. The sheet resistivity of the resulting film was 4.5 x 10-3 ohms/square.
Example 2
In accordance with the procedure of Example 1, a gold-platinum conductor ink was prepared from the following formulation:
Ingredient Percent
Gold powder 67.23
Platinum powder 16.81
Glass frit of Example 1 1.26
Bismuth oxide 1.26
Bismuth nitrate pentahydrate 0.84
Organic vehicle 12.60
The organic vehicle consisted of: ethyl cellulose (0.70); terpineol (5.43); butyl carbinol acetate (3.82); Texanol (2.23); and Thixatrol (0.42).
The ink was printed and fired in accordance with the procedure of,Example 1 and the resulting film found to have a sheet resistivity of 66 x 10-3 ohms/square.
Example 3
In accordance with the procedure of Example 1, a silver-palladium conductor ink was prepared from the following formulation:
Ingredient Percent
Silver powder 51.09
Palladium powder 21.90
Glass frit of Example 1 3.29
Bismuth oxide 3.28
Bismuth nitrate pentahydrate 0.73
Organic vehicle 19.71
The organic vehicle consisted of: ethyl cellulose (0.78); terpineol (17.56); butyl carbinol acetate (1.33) and Thixatrol (0.04).
The ink was printed and fired in accordance with the procedure of Example 1 and the resulting film found to have a sheet resistivity of 58x 10-3 ohms/square.
Example 4
In accordance with the procedure of Example 1, a silver-palladium-platinum conductor ink was prepared from the following formulation:
Ingredient Percent
Silver powder 46.80
Palladium powder 12.32
Platinum powder 7.39
Glass frit of Example 1 6.90
Bismuth oxide 6.89
Organic vehicle 19.70
The organic vehicle consisted of: ethyl cellulose (1.13); terpineol (13.94); butyl carbinol acetate (4.48); and Thixatrol (0.15).
The ink was printed and fired in accordance with the- procedure of Example 1 and the resulting film found to have a sheet resistivity of 85x 10-3 ohms/square.
Example 5
Ruthenium resistor inks were prepared in accordance with the procedure of Example 1 from the following formulations:
Percent
Formulation RuO2 Glass frit Vehicle
A 21.43 50.00 28.57
B 11.54 65.38 23.08
C 5.38 71.54 23.08
The glass frit in each instance consisted of: BaO (51.59); CaO (12.58): B#O#(15.62); and SiO2 (20.21). The organic vehicle consisted of à 6 percent solution of ethyl cellulose in Texanol.
The inks were screened and fired in air according to the procedure of Example 1. Various conductor terminations were initially applied and fired for the above formulations. The sheet resistivity was determined in each instance and is reported in the following table.
Table
Termination Termination Sheet resistivity
Ink No. metal formulation kilo-ohm per square
A Au Ex.1 0.107
B B Ag-Pd Ex.2 11.8
C Ag-Pd Ex. 3 1273.0
The results demonstrate the compatibility of the subject resistors and conductors.
Claims (28)
1. An air-fireable conductor or resistor ink suitable for forming a film on a porcelain-coated metal circuit board comprising a functional component, a glass frit and a suitable organic vehicle, wherein the glass frit consists of from about 40 to about 55 percent by weight of barium oxide, from about 10 to about 15 percent by weight of calcium oxide, from about 14 to about 25 percent by weight of boron trioxide, and from about 13 to about 23 percent by weight of silicon dioxide.
2. An air-fireable ink in accordance with Claim 1, wherein said ink is a resistor ink, said functional component is ruthenium dioxide and said ink comprises
a) from about 2 to about 60 percent by weight of ruthenium dioxide;
b) from about 25 to about 80 percent by weight of said glass frit; and
c) from about 10 to about 35 percent by weight of said vehicle.
3. An air-fireable ink In accordance with Claim 2, wherein said glass frit consists of about 52 percent by weight of barium oxide, about 12 percent by weight of calcium oxide, about 16 percent by weight of boron trioxide, and about 20 percent by weight of silicon dioxide.
4. An air-fireable ink in accordance with Claim 2, wherein said ink comprises from about 5 to about 25 percent by weight of ruthenium dioxide, from about 50 to about 75 percent by weight of said glass, and from about 20 to about 30 percent by weight of said vehicle.
5. An air-fireable ink in accordance with Claim 2, 3 or 4, wherein said ink contains up to about 10 percent by weight of a temperature coefficient of resistance modifier selected from the group consisting of manganese dioxide, cadmium oxide, and cuprous oxide.
6. An air-fireable ink in accordance with Claim 1, wherein said ink is a conductor ink, said functional component is a precious metal and said Ink comprises:
a) from about 60 to about 90 percent by weight of a precious metal powder;
b) from about 1 to about 15 percent by weight of said glass;
c) from about 1 to about 15 percent by weight of bismuth oxide, wherein bismuth oxide is present in admixture with the precious metal or as a component of the glass; and
d) from about 8 to about 30 percent by weight of said vehicle.
7. An air-fireable ink in accordance with Claim 6, wherein said ink comprises: from about 70 to about 85 percent by weight of said precious metal; from about 1 to about 7 percent by weight of said glass; from about 1 to about 7 percent by weight of,,bismuth oxide; and from about 10 to about 25 percent by weight of said vehicle.
8. An air-fireable Ink in accordance with Claim 6 or 7, wherein said glass consists of about 52 percent by weight of barium oxide, about 12 percent by weight of calcium oxide, about 19 percent by weight of boron trioxide, and about 17 percent by weight of silicon dioxide.
9. An air-fireable ink in accordance with Claim 6,7 or 8, wherein said precious metal is selected from the group consisting of gold, silver, platinum, palladium, rhodium, and mixtures thereof.
10. An air-fireable ink in accordance with Claim 9 wherein said precious metal is gold.
11. An air-fireable ink in accordance with Claim 9 wherein said precious metal is a mixture of gold and platinum.
12. An air-fireable ink in accordance with Claim 9 wherein said precious metal is a mixture of silver and palladium.
13. An air-fireable ink in accordance with Claim 9 wherein said precious metal is a mixture of silver, palladium, and platinum.
14. An air-fireable ink in accordance with any of Claims 6-1 3, wherein the weight ratio of bismuth oxide to glass is from about 3:1 to about 1:3.
1 5. An assembly comprising a porcelain-coated metal circuit board having on a portion of the surface thereof a coating of an air-fireable conductor or resistor ink comprising a functional component, a glass and a suitable organic vehicle, wherein the glass consists of from about 40 to about 55 percent by weight of barium oxide, from about 10 to about 1 5 percent by weight of calcium oxide, from about 14 to about 25 percent by weight of boron trioxide, and from about 13 to about 23 percent by weight of silicon dioxide.
16. An assembly in accordance with Claim 15, wherein said ink is a resistor ink, said functional component is ruthenium dioxide and said ink comprises:
a) from about 2 to about 60 percent by weight of ruthenium dioxide;
b) from about 25 to about 80 percent by weight of said glass; and
c) from about 10 to about 35 percent by weight of said vehicle.
17. An assembly in accordance with Claim 15, wherein said metal is steel.
18. An assembly in accordance with Claim 15 wherein said ink is a conductor ink, said functional component is a precious metal and said ink comprises:
a) from about 60 to about 90 percent by weight of said precious metal;
b) from about 1 to about 15 percent by weight of said glass;
c) from about 1 to about 1 5 percent by weight of bismuth oxide, wherein bismuth oxide is present in admixture with the precious metal or as a component of the glass; and
d) from about 8 to about 30 percent by weight of said vehicle.
19. An assembly in accordance with Claim 18, wherein said precious metal is selected from the group consisting of gold, silver, platinum, palladium, rhodium, and mixtures thereof.
20. A process for forming a resistor or conductor film as part of a circuit on a porcelain-coated circuit board comprising applying and firing onto said board an ink composition according to any preceding claim.
21. An electronic assembly comprising a porcelain-coated metal circuit board having a circuit thereon, said circuit containing a resistor film or conductor film formed by applying and firing in air a resistor or conductor ink comprising a functional component, a glass frit and a suitable organic vehicle, wherein said glass consists of from about 40 to about 55 percent by weight of barium oxide, from about 10 to about 15 percent by weight of calcium oxide, from about 14 to about 25 percent by weight of boron trioxide, and from about 13 to about 23 percent by weight of silicon dioxide.
22. An electronic assembly in accordance with Claim 21, wherein said ink is a resistor ink, said functional component is ruthenium dioxide and said ink comprises:
a) from about 2 to about 60 percent by weight of ruthenium dioxide;
b) from about 25 to about 80 percent by weight of said glass frit; and
c) from about 10 to about 35 percent by weight of said vehicle.
23. An electronic assembly in accordance with Claim 21, wherein said ink is a conductor ink, said functional component is a precious metal and said ink comprises:
a) from about 60 to about 90 percent by weight of said precious metal;
b) from about 1 to about 15 percent by weight of said glass;
c) from about 1 to about 15 percent by weight of bismuth oxide, wherein bismuth oxide is present in admixture with the precious metal or as a component of the glass; and
d) from about 8 to about 30 percent by weight of said vehicle.
24. An assembly according to claim 16 or claim 22, wherein said resistor ink is in accordance with any of claims 3-5.
25. An assembly according to claim 18 or claim 23, wherein said conductor ink is in accordance with any of claims 7-14.
26. An air-fireable ink substantially as hereinbefore described.
27. A circuit board assembly substantially as hereinbefore described.
28. An electronic assembly substantially as hereinbefore described.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US28093681A | 1981-07-06 | 1981-07-06 |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2107302A true GB2107302A (en) | 1983-04-27 |
GB2107302B GB2107302B (en) | 1985-05-09 |
Family
ID=23075248
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB08219147A Expired GB2107302B (en) | 1981-07-06 | 1982-07-02 | Air-fireable thick film inks |
Country Status (6)
Country | Link |
---|---|
JP (1) | JPS5815576A (en) |
KR (1) | KR880002063B1 (en) |
CA (1) | CA1173644A (en) |
DE (1) | DE3224573A1 (en) |
FR (1) | FR2508922B1 (en) |
GB (1) | GB2107302B (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4946837A (en) * | 1984-06-08 | 1990-08-07 | Takeda Chemical Industries, Ltd. | Cephem compounds |
US6362119B1 (en) | 1999-06-09 | 2002-03-26 | Asahi Glass Company, Limited | Barium borosilicate glass and glass ceramic composition |
EP1770721A2 (en) * | 2005-10-03 | 2007-04-04 | Shoei Chemical Inc. | Resistor composition and thick film resistor |
EP2749611A2 (en) * | 2012-12-28 | 2014-07-02 | Dip-Tech Ltd. | Noble metal based ink |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4537703A (en) * | 1983-12-19 | 1985-08-27 | E. I. Du Pont De Nemours And Company | Borosilicate glass compositions |
US4722853A (en) * | 1985-08-12 | 1988-02-02 | Raychem Corporation | Method of printing a polymer thick film ink |
WO1996017025A1 (en) * | 1994-12-01 | 1996-06-06 | Eckart-Werke Standard Bronzepulver-Werke Carl Eckart Gmbh & Co. | Conductive ink |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3775347A (en) * | 1969-11-26 | 1973-11-27 | Du Pont | Compositions for making resistors comprising lead-containing polynary oxide |
US3876433A (en) * | 1973-12-28 | 1975-04-08 | Du Pont | Bismuth-containing silver conductor compositions |
US3974107A (en) * | 1974-03-27 | 1976-08-10 | E. I. Dupont De Nemours And Company | Resistors and compositions therefor |
JPS5130004A (en) * | 1974-09-05 | 1976-03-13 | Matsushita Electric Ind Co Ltd | TENSHAYOTEIKOPEESUTONOSEIZOHOHO |
JPS5222790A (en) * | 1975-08-14 | 1977-02-21 | Sumitomo Metal Mining Co Ltd | Base material for thick film conductive paste |
JPS5399499A (en) * | 1977-02-09 | 1978-08-30 | Hitachi Chemical Co Ltd | Ink for variable resistance |
JPS5534211A (en) * | 1978-08-31 | 1980-03-10 | Toppan Printing Co Ltd | Calcining ink composition |
US4230493A (en) * | 1978-09-22 | 1980-10-28 | E. I. Du Pont De Nemours And Company | Gold conductor compositions |
US4286251A (en) * | 1979-03-05 | 1981-08-25 | Trw, Inc. | Vitreous enamel resistor and method of making the same |
DE3140969A1 (en) * | 1980-10-17 | 1982-06-16 | RCA Corp., 10020 New York, N.Y. | Copper conducting ink |
-
1982
- 1982-03-30 CA CA000399735A patent/CA1173644A/en not_active Expired
- 1982-06-30 FR FR8211480A patent/FR2508922B1/en not_active Expired
- 1982-06-30 JP JP57114774A patent/JPS5815576A/en active Granted
- 1982-07-01 DE DE19823224573 patent/DE3224573A1/en not_active Withdrawn
- 1982-07-02 GB GB08219147A patent/GB2107302B/en not_active Expired
- 1982-07-06 KR KR8203012A patent/KR880002063B1/en active
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4946837A (en) * | 1984-06-08 | 1990-08-07 | Takeda Chemical Industries, Ltd. | Cephem compounds |
US6362119B1 (en) | 1999-06-09 | 2002-03-26 | Asahi Glass Company, Limited | Barium borosilicate glass and glass ceramic composition |
EP1770721A2 (en) * | 2005-10-03 | 2007-04-04 | Shoei Chemical Inc. | Resistor composition and thick film resistor |
EP1770721A3 (en) * | 2005-10-03 | 2007-10-03 | Shoei Chemical Inc. | Resistor composition and thick film resistor |
US7476342B2 (en) | 2005-10-03 | 2009-01-13 | Shoei Chemical Inc. | Resistor composition and thick film resistor |
EP2749611A2 (en) * | 2012-12-28 | 2014-07-02 | Dip-Tech Ltd. | Noble metal based ink |
EP2749611A3 (en) * | 2012-12-28 | 2014-08-27 | Dip-Tech Ltd. | Noble metal based ink |
Also Published As
Publication number | Publication date |
---|---|
FR2508922B1 (en) | 1987-04-17 |
GB2107302B (en) | 1985-05-09 |
CA1173644A (en) | 1984-09-04 |
FR2508922A1 (en) | 1983-01-07 |
KR840000623A (en) | 1984-02-25 |
KR880002063B1 (en) | 1988-10-14 |
DE3224573A1 (en) | 1983-01-20 |
JPS5815576A (en) | 1983-01-28 |
JPH0153907B2 (en) | 1989-11-16 |
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Date | Code | Title | Description |
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PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19930702 |