WO2004066316A1 - 導電性ペースト及びその製造方法並びにその導電性ペーストを用いた回路基板及びその製造方法 - Google Patents
導電性ペースト及びその製造方法並びにその導電性ペーストを用いた回路基板及びその製造方法 Download PDFInfo
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- WO2004066316A1 WO2004066316A1 PCT/JP2004/000460 JP2004000460W WO2004066316A1 WO 2004066316 A1 WO2004066316 A1 WO 2004066316A1 JP 2004000460 W JP2004000460 W JP 2004000460W WO 2004066316 A1 WO2004066316 A1 WO 2004066316A1
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- conductive paste
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Classifications
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- 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
- H05K3/00—Apparatus or processes for manufacturing printed circuits
- H05K3/40—Forming printed elements for providing electric connections to or between printed circuits
- H05K3/4038—Through-connections; Vertical interconnect access [VIA] connections
- H05K3/4053—Through-connections; Vertical interconnect access [VIA] connections by thick-film techniques
- H05K3/4069—Through-connections; Vertical interconnect access [VIA] connections by thick-film techniques for via connections in organic insulating substrates
-
- 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
- H01B1/20—Conductive material dispersed in non-conductive organic material
- H01B1/22—Conductive material dispersed in non-conductive organic material the conductive material comprising metals or alloys
-
- 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
- H05K1/095—Dispersed materials, e.g. conductive pastes or inks for polymer thick films, i.e. having a permanent organic polymeric binder
-
- 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
- H05K2201/00—Indexing scheme relating to printed circuits covered by H05K1/00
- H05K2201/02—Fillers; Particles; Fibers; Reinforcement materials
- H05K2201/0203—Fillers and particles
- H05K2201/0263—Details about a collection of particles
- H05K2201/0266—Size distribution
-
- 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
- H05K2201/00—Indexing scheme relating to printed circuits covered by H05K1/00
- H05K2201/03—Conductive materials
- H05K2201/0332—Structure of the conductor
- H05K2201/0335—Layered conductors or foils
- H05K2201/0355—Metal foils
-
- 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
- H05K2203/00—Indexing scheme relating to apparatus or processes for manufacturing printed circuits covered by H05K3/00
- H05K2203/14—Related to the order of processing steps
- H05K2203/1461—Applying or finishing the circuit pattern after another process, e.g. after filling of vias with conductive paste, after making printed resistors
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49002—Electrical device making
- Y10T29/49117—Conductor or circuit manufacturing
- Y10T29/49124—On flat or curved insulated base, e.g., printed circuit, etc.
- Y10T29/49126—Assembling bases
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
Definitions
- the present invention relates to a conductive paste, a method of manufacturing the same, a circuit board using the conductive paste, and a method of manufacturing the same.
- the present invention relates to a composition of a conductive paste used for a circuit-forming substrate used for various electronic devices, and in particular, to a conductive paste which can be used for filling a via hole for electrically connecting each layer in a multilayer substrate.
- the present invention relates to a method for manufacturing a conductive paste, a circuit board using the conductive paste, and a method for manufacturing the same.
- the circuit-forming substrate has an inner via hole structure using a conductive paste that can realize higher-density connection between layers at a specified position, instead of the connection between layers by through-hole processing and plating, which has been widely used in the past. Has been proposed.
- FIGS. 7A to 7G are process cross-sectional views illustrating a conventional circuit forming substrate manufacturing process.
- a release film 11 formed by applying a release agent such as a silicone resin to a PET (polyethylene terephthalate) film is applied to an insulating substrate 12. Prepare what is stuck on both sides of.
- the insulating substrate 12 is, for example, a material obtained by impregnating a woven or nonwoven fabric made of inorganic or organic fibers with a thermosetting resin.
- a composite material in which a glass fiber woven fabric is impregnated with an epoxy resin or a composite material in which an aramide fiber nonwoven fabric is impregnated with an epoxy resin has a semi-cured state, i.e., a B-stage pre-prepared resin.
- a sheet is, for example, a material obtained by impregnating a woven or nonwoven fabric made of inorganic or organic fibers with a thermosetting resin.
- a through hole 13 is formed at a predetermined position of an insulating substrate (prepredsheet) 12 made of a prepred sheet using a laser or a drill.
- a conductive paste 14 is filled into the through hole 13 from above the release film 1.
- the paste may be discharged from a nozzle such as a dispenser.
- the insulating substrate (prepredder sheet) 12 may be filled from either side, but from the viewpoint of productivity and cost, it is realistic to use a tape (printer) tape as shown in Fig. 7C. (Not shown), and filling is often performed by a printing method using a squeegee 15 such as urethane rubber.
- the releasable film 11 plays a role as a printing mask and a role as a contamination preventing film for the insulating substrate (prepredder sheet) 12.
- FIG. 8A and FIG. 8B correspond to FIG.7E and FIG.7F, respectively.
- FIG.8A and FIG.8B correspond to FIG.7E and FIG.7F, respectively.
- These drawings schematically show a cross section of the vial table.
- the conductive paste 14 has conductive particles 18 and a binder component 19 mainly composed of a thermosetting resin or the like. Agent.
- the thickness of the insulating substrate (pre-preplated sheet) 1 2 is compressed from 1 ⁇ of FI G. 88 to t of FI G. 8 B by heating and pressing, and the conductive particles and the conductive particles and metal foil are compressed.
- the conduction is obtained by the contact at the interface of 16.
- the compression ratio of the base material can be expressed as follows.
- Substrate compressibility (%) (t.—) no t. X 1 0 0)
- t D is the thickness of the insulating substrate (pre-precipitate) 12 before heating and pressing and after heating and pressing, respectively.
- the metal foil 16 on both sides is selectively etched to form a wiring pattern 17, thereby obtaining a circuit forming substrate.
- the inner via connection technology using the conductive paste 14 has a relatively simple process, high productivity, and can realize a high-density circuit-forming substrate at relatively low cost. ⁇
- the resistance value per via is extremely low, less than a few ⁇ , showing high connection reliability even in load tests by heating, humidification, and thermal shock.
- FIG. 9 shows the cross-section of the insulating substrate (prepredder sheet) 12 after the conductive paste 14 shown in FI G. 7 C has been printed and filled into the through hole 13 using a squeegee 15.
- FIG. 3 is a schematic cross-sectional view.
- FIG. 9 shows a state in which a layer of the liquid binder component 19 is formed on the surface of the release film 11 and a small amount of the conductive particles 18 remain.
- the liquid binder component 19 is filtered off from the conductive paste 14 and remains on the surface of the release film 11.
- This process is a continuous printing process in which new insulating substrates (prepredder sheets) 12 are repeatedly filled one after another, so that the liquid binder is successively filtered off from the conductive paste, and the solid conductive material gradually becomes solid.
- the conductive particles are rich, that is, the existence ratio of the conductive particles in the conductive paste increases, the viscosity increases.
- thermosetting resin proceeds due to a change in the dispersion state of the conductive particles in the liquid binder component and the shearing shear stress.
- This increase in viscosity significantly worsens the filling of fine through holes. Therefore, it is considered that the composition capable of suppressing the increase in the viscosity, that is, the reduction in the viscosity, leads to an improvement in the number of processed insulating substrates (prepredder sheets) 12.
- this conductive paste has the following three problems, and it is difficult to solve all of them and achieve both the improvement of the reliability of the conductive connection and the cost reduction by improving the productivity. .
- the conductive paste contain as many conductive particles as possible.
- the mixing ratio at which the paste can be formed there is a limit to the mixing ratio at which the paste can be formed, and if the viscosity is too high, the filling property to the via is impaired.
- the productivity in the step of filling the via with the conductive paste as described above, the number of processed insulating substrates (prepredder sheets) 12 is more effective as the viscosity of the conductive paste is lower. is there. Therefore, a low viscosity conductive base containing many conductive particles is required. Since the inner via hole is formed by heating and pressing the metal foil 16 and the insulating substrate 12, if a large amount of volatile components are contained in the conductive paste ⁇ ⁇ 4, the vapor inside the inner via hole during heating The pressure may increase and a connection failure may occur due to swelling. Therefore, the conductive paste must maintain low volatility.
- the water content is low, and when a solvent is used for viscosity adjustment as used in a generally known paste for forming a thick film circuit, the amount of addition is limited, so that it is as small as possible. Is more desirable.
- a binder mainly composed of a thermosetting resin is an important factor for the reliability of connection of the inner via hole.
- the type of resin or hardener to be selected is determined according to the characteristics required for the circuit-forming substrate and the inner via hole, taking into consideration the matching with the insulating substrate (prepredder sheet) 12. For this reason, there may be a case where the selection based on the limitation of the resin viscosity cannot be freely performed or a case where the mixing ratio with the conductive particles cannot be freely blended.
- the present invention solves the above problems. In other words, we want to include as many conductive particles as possible for the reliability of conductive connection. The conflicting demands of reducing the content of particles can be solved. It is another object of the present invention to provide a conductive paste suitable for a via-hole conductor, and to provide a circuit forming substrate using the same and a method for manufacturing the same. Disclosure of the invention
- the conductive paste of the present invention is composed of primary particles and aggregated particles obtained by aggregating the primary particles, and has an average particle size of 0.5 to 20 tm and a specific surface area of 0.07 to 1.7 m 2 / g of the conductive particles and a binder mainly composed of a thermosetting resin.
- the conductive paste Bok of the present invention has an average particle diameter of 0. 5 to 2 0 m, a specific surface area of 0.0 Ryo ⁇ . A 7 m 2 Z g, and at least two peaks of particle size distribution
- This is a conductive paste composed of conductive particles having the following characteristics and a binder containing a thermosetting resin as a main component.
- it is composed of conductive particles formed by mixing at least two or more conductive particles having different particle size distributions, and a binder containing a thermosetting resin as a main component.
- the conductive paste of the present invention is composed of conductive particles formed by mixing at least two or more conductive particles having different particle size distributions, and a binder mainly containing a thermosetting resin.
- the conductive particles in the conductive paste can be dispersed in a binder containing a thermosetting resin as a main component with improved dispersibility.
- a conductive paste with reduced viscosity can be obtained.
- the state of contact between the conductive particles inside the inner via hole can be improved, and variations in the state of contact can be eliminated.
- a conductive paste is provided by a method of manufacturing a conductive paste including a step of preparing conductive particles, a step of mixing them, and a step of adding and kneading a binder to the conductive paste.
- the conductive paste in the conductive paste is dispersed in a binder containing a thermosetting resin as a main component with good dispersibility, so that the viscosity of the conductive paste is reduced.
- the contact state between the conductive particles inside one via hole can be improved, and the variation in the contact state can be eliminated.
- This provides an excellent conductive paste that can both improve connection reliability and reduce costs by improving productivity, and realizes a highly reliable circuit board using the conductive paste. Is what you do.
- the method for producing a circuit board of the present invention comprises the steps of: obtaining a primary particle average diameter; and obtaining an aggregated particle average diameter, in a method for measuring conductive particles including primary particles and aggregated particles obtained by aggregation of the primary particles.
- the present invention provides a method for measuring conductive particles including a step of calculating by the following equation, whereby a conductive particle contained in a conductive paste is numerically measured. Then, based on such a measurement method, a conductive paste is manufactured, and a circuit-formed substrate is manufactured using the conductive paste.
- the conductive particles in the conductive paste are dispersed in a binder containing a thermosetting resin as a main component by increasing the dispersibility, whereby the viscosity of the conductive paste is reduced, and The contact state between the conductive particles inside the inner via hole can be improved, and the variation in the contact state can be eliminated.
- an excellent conductive paste that can achieve both improved connection reliability and reduced cost by improving productivity is provided, and a highly reliable circuit formation using the conductive paste is provided.
- a substrate can be realized.
- the circuit forming substrate of the present invention includes an insulating substrate and a plurality of wiring patterns formed on the insulating substrate. And a via-hole conductor for electrically connecting a wiring pattern to the wiring pattern.
- the via-hole conductor is composed of primary particles and agglomerated particles obtained by aggregating primary particles, and has an average particle size of 0.5.
- a conductive paste comprising conductive particles having a specific surface area of 0.07 to 1.7 m 2 Zg and a binder containing a thermosetting resin as a main component.
- a conductive material having an average particle size of 0.5 to 20 Atm, a specific surface area of 0.07 to 1.7 m 2 / g, and having at least two peaks in the particle size distribution.
- FIG. 1 is a schematic diagram showing conductive particles according to Embodiment 1 of the present invention
- FIG. 2 is a schematic diagram of other conductive particles according to Embodiment 1 of the present invention
- FIG. I s a schematic diagram of aggregating conductive particles different from the first embodiment of the present invention
- FIG. 4A to FIG. 4B show the particle size distribution of the conductive particles according to the third embodiment of the present invention.
- FIG. 5 is a diagram showing a correlation between cohesion, viscosity and resistance value
- FIGS. 6A to 6G are diagrams showing a method for manufacturing a circuit-formed substrate of the present invention.
- Figure, FI G. 7 A to FI G. 7 G are process diagrams showing a conventional method for manufacturing a circuit-formed substrate
- FIG. 8 A to FI G. 8 B are processes showing the mechanism of the occurrence of conduction in the circuit-formed substrate.
- FIG. 9 is a cross-sectional view showing a state after the conductive paste is filled into the through-hole.
- Embodiment 1 will be described with reference to the drawings.
- the cohesiveness and particle size distribution of metal powders such as copper, silver or gold, alloy powders, or metal powders coated with dissimilar metals, which are conductive particles constituting the conductive paste, are described.
- High control As a device for measuring the particle size distribution of conductive particles, a laser diffraction / scattering type is widely used. In the powder industry, Nikkiso's microtrak is used for the wet type, and SYMPATECH ELOS is used for the dry type. Such devices are well known.
- FIG. 1 is a plan view schematically showing the state of aggregation of the copper powder of the conductive paste according to the first embodiment.
- copper particles as conductive particles according to the first embodiment are aggregates of spherical primary particles 1 and aggregated particles 2 in which two or more primary particles 1 are aggregated.
- the average particle diameter 0.. 5 to 2 0 m
- the specific surface area is 0. 0 7 ⁇ . 7 m 2 Z g
- the degree of agglomeration is one. 6 0. This increases the chance of contact between the conductive particles and, as a result, has the effect of lowering the via hole conductor resistance.
- the degree of aggregation is an index indicating the degree of aggregation of the aggregated particles, and can be defined as a value obtained by dividing the average diameter of the aggregated particles by the average diameter of the primary particles. That is, it can be expressed as (aggregation degree-average diameter of aggregated particles / average diameter of primary particles).
- This method of measuring particle size distribution of deviation is not a measurement method that takes cohesiveness into consideration, so the results of the obtained particle size distribution and the viscosity of the conductive paste, the filling property to the via, and the resistance of the via-hole conductor It could not be completely correlated with the values. Therefore, the present invention takes into consideration the cohesiveness of the conductive particles and pays attention to the degree of agglomeration as an index.
- the laser diffraction scattering method As an example of the method of measuring the degree of aggregation of the conductive particles according to the present invention, the laser diffraction scattering method Assuming that the average particle size obtained by using the particle size distribution measuring device described above is the average particle size of the aggregated particles, and the average particle size obtained from the image analysis of the SEM image is the average particle size of the primary particles, the degree of agglomeration is as described above.
- Aggregation degree average diameter of aggregated particles / average diameter of primary particles
- the SEM image is used for calculating the average primary particle diameter, but an image taken by a CCD camera or an optical microscope may be used.
- data from a particle size distribution measuring device that processes particle information such as FPIA available from Sysmex Corporation or a multi-image analyzer from Beckman Cole Yuichi may be used.
- the cohesiveness of the particles which could not be achieved by a single particle size distribution measuring device, can be given as the cohesion degree.
- FIGS. 2 and 3 are plan views schematically showing conductive particles having a different degree of aggregation from the conductive particles described in FIG.
- the aggregation in FIG.2 and FIG.3 was 3.90 and 1.000, respectively.
- the conductive particles shown in FIG. 2 are more cohesive than those shown in FIG.
- the conductive particles shown in FIG. 3 realize a separated state in which the primary particles 1 hardly aggregate.
- the degree of agglomeration should be 1.0.
- the difference between the primary particle and agglomerated particle measurement devices and the method of spherical approximation It has a slight variation due to factors such as:
- the conductive particles according to the present invention preferably have an agglomeration degree in the range of 1.05 to 3.90. This reduces the paste viscosity while maintaining the connection reliability of the Malawi hole conductor. It can be kept low.
- the cohesion is less than 1.05, the effect of reducing the viscosity of the conductive paste is remarkable, but the resistance value of the via hole conductor is deteriorated, and the reliability of the conductive connection is impaired.
- the cohesion exceeds 3.90, the reliability of the conductive connection of the via-hole conductor can be satisfied, but the dispersibility of the conductive paste is not improved, and the effect of reducing the viscosity is reduced.
- Various types of conductive particles can be candidates. However, in practice, it is preferable to select conductive particles formed by a chemical reduction method, an electrolytic method, a dry atomization method, or a pulverization method by a wet method.
- a copper powder precipitated by a wet chemical reduction reaction is dried. The value of the cohesion degree of this copper powder was 4.60.
- a method of controlling the degree of aggregation of the copper powder a method of alleviating the state of aggregation of individual particles and reducing the degree of aggregation of the particles by applying energy to the particles in the state of aggregation and subjecting them to a pulverizing treatment.
- the energy may be applied by directly applying an air current such as a jet jet to the particles, or by applying the particles to a rotating device with centrifugal force so that wind energy is relatively applied.
- an air classifier “Turbo Classifier” manufactured by Nisshin Engineering.
- the primary use of this device is to classify particles according to particle size.
- it was used for the purpose of giving wind energy to the aggregated particles.
- the purpose was not to classify but to pulverize.
- the amount of energy applied during pulverization was controlled by the rotation speed, the number of treatments, and the treatment time, etc., and several types of copper powder were obtained with a cohesion value of 1.60 and other values. .
- the degree of aggregation is 3.90 or less, the lower the degree of aggregation, the greater the effect of reducing viscosity. Therefore, it can be subjected to a pulverizing process.
- the conductive particles having an agglomeration degree of 2.5 may be subjected to a pulverizing treatment, and the agglomeration degree may be reduced to less than, eg, 1.60.
- the conductive particles of the present invention desirably have a surface oxygen concentration of 1.0 wt% or less. Thereby, good conductor resistance with less oxide film on the conductor surface can be obtained.
- the agglomeration degree exceeds 1.0 wt%, the electrical connection between the particles is prevented by the insulating layer of the surface oxide, and the oxygen atoms on the surface become one component of the binder mainly composed of the thermosetting resin.
- a phenomenon such as an increase in the viscosity of the conductive paste accompanied by a chemical or physical bond with the conductive paste occurs.
- the concentration of water adsorbed on the conductive particles is desirably 1 000 ppm or less, whereby a via hole conductor having excellent printing characteristics and high reliability can be formed.
- concentration of the adsorbed water exceeds 1 000 ppm, the adsorption reaction is promoted, the pot life is shortened, the viscosity of the conductive paste is increased, and the printability is reduced. In addition, it may cause deterioration of the curability of the thermosetting resin.
- concentration of adsorbed water can be relatively easily reduced to 1,000 ppm or less by drying the conductive particles.
- the primary particles of the conductive particles in the present invention are spherical for convenience of explanation. However, if it is assumed that U particles are formed by a wet chemical reduction method, an electrolytic method, a dry atomization method, or a pulverization method, fine particles having irregularities instead of true spheres should be used. It should be understood that this is a clump of particles and includes particles with a slightly distorted shape.
- copper powder with a cohesion of 1.60 obtained by subjecting copper powder formed by wet reduction method to conductive particles to 87.5 wt% was obtained.
- the dimer acid diglycidyl ester type epoxy resin (Epicoat 871 manufactured by Japan Epoxy Resin Co., Ltd.) was set to 10.9 wt%, and the amine adduct type hardener (Amicoh MY-24 manufactured by Ajinomoto Fine Techno Co., Ltd.) was set at 1.6 wt%.
- the binder obtained by the addition was kneaded using a ceramic three-roll mill to obtain a conductive paste.
- the content is set to 87.5 wt% using copper powder as the conductive particles, but the content in volume is important and differs depending on the specific gravity of the conductive particles used.
- the content by volume of the conductive particles according to the present invention is desirably in the range of 30 to 70 V 0 I%, and when it exceeds 70 V O I%, the binder content is less than 30 V 0 I%.
- the viscosity of the conductive paste increases significantly, making it extremely difficult to paste.
- dimer acid diglycidyl ester type epoxy resin was used as the thermosetting resin as a component of the conductive paste.
- some properties are added, for example, increasing the crosslink density, adding flexibility, and increasing the glass transition point (T g). can do.
- glycidyl ether type epoxy resins such as bisphenol F type epoxy resin, bisphenol A type epoxy resin, bisphenol AD type epoxy resin, alicyclic epoxy resin, glycidylamine type epoxy resin, dalicidyl ester type epoxy resin Epoxy resins selected from resins and the like may be used alone or in combination of two or more.
- a polyimide resin, a cyanate ester resin, a phenol resin resin, or the like may be used as one component of the binder.
- the conductive paste described above is a solventless type.
- solvent dispersing agents such as butyl cellulose, butyl cellulose, acetyl acetate, ethyl carbitol, ethyl carbyl, etc. May be added.
- the amount of volatilization as a conductive paste be 4.owt? Or less based on the total weight. Thereby, high reliability of the Malawi hole conductor can be secured. If the amount of volatilization exceeds 4. Owt%, the volatile component inside the via hole increases, so that the reliability of the conductive connection of the via hole conductor is degraded or swelling occurs.
- the viscosity of the obtained epoxy-based copper paste was measured with an E-type viscometer, and at 0.5 rpm (shear speed Is s') using an R14Z3 ° cone, It was 18 Pas, and at 5 rpm it was 38 Pas.
- copper powders having different degrees of agglomeration were used, but the production method is the same as described above, and therefore the description is omitted, and the viscosity of the obtained conductive paste will be described in the following second embodiment.
- FIGS. FIG.6A to FIG.6G are cross-sectional views showing the steps of manufacturing the circuit formation substrate according to the present invention.
- a non-woven fabric of aramide fiber is impregnated with epoxy resin, and its thickness is 120 / Cm and its size is 50 OmmX 34 Omm in a semi-cured state (B stage).
- a 20 m thick PET (polyethylene terephthalate) film formed by applying a release agent such as silicone to both sides of an insulating substrate (prepredder sheet).
- a through-hole 13 with a via diameter of 200 tm was formed at a predetermined position of the insulating substrate (pre-precipitate) 12 (base material A) with a carbon dioxide gas laser.
- the conductive paste 4 prepared in Embodiment 1 was put into the filling machine (not shown) from the top of the releasable film 11 and the through hole was formed. Filled into 13.
- the releasable film 11 is used as a printing mask, ⁇ ) ⁇ 2 Plays a role as a pollution control film.
- the release film 11 on both sides of the insulating substrate (pre-pre-dated sheet) 12 is peeled off, and then the insulating substrate (pre-prepared sheet) is removed as shown in FI G. 6E.
- metal foil 16 from both sides of 12 sandwich it between 18 jm thick copper foils on both sides.
- the insulating substrate (prepredder sheet) 12 and the metal foil 16 are bonded as shown in FIG. 6F.
- the inside of the insulating substrate (prepreg sheet) 12 and the through hole 13 is filled, and the conductive paste 4 is compressed. Thereby, the metal foils 16 on both sides are electrically connected by the conductive paste 4.
- the metal foil 16 on both sides is selectively etched to form a wiring pattern 17 to obtain a circuit forming substrate.
- a copper foil having a surface roughness of 18 tm is used as the metal foil in Embodiment 2, but a single-sided copper foil may be used.
- a copper foil with a carrier having a thickness of 3 or 12 ⁇ , which is thinner, or a metal foil other than the copper foil can be used.
- the conditions for the heating and pressurization of the heat press may be set according to the composition of the selected insulating substrate (pre-precipitate) 12 or conductive paste.
- the heating and pressing conditions in the second embodiment were set at a pressing temperature of 200 ° C., a pressure of 4.9 MPa (50 kgf Zcm 2 ), and a pressing time of 60 minutes.
- a test pattern having a total of 30,000 via holes in which resistance measuring pieces each having 500 vias as a series circuit are arranged in 5 rows ⁇ 12 columns is provided. I tried to make.
- a circuit forming substrate having a via diameter of ⁇ 150 im was obtained.
- Viscosity is measured at R14 / 3 ° cone, 0.5rpm (Toki Sangyo RE-80U)
- the board resistance value is the average value of the series resistance value for 500 via holes (including the wiring resistance of 0.7 ⁇ ).
- the conductive particles of the conductive paste according to Embodiment 2 have a degree of agglomeration in the range of 105 to 3.90.
- the substrate resistance value the average value of the series resistance values of the 500 vias is shown.
- an extremely good electrical conductivity of 1 112 ⁇ (Example 2) to 1.28 ⁇ (Example 1) was obtained.
- the agglomeration degree of the conductive particles exceeds 3.90, the viscosity of the conductive paste becomes extremely high due to the agglomeration property, and the through-holes 1 provided in the insulating substrate (prepredential) 12 The filling property when filling the conductive paste into 3 is impaired. Also, when the release film 11 is peeled off, the conductive paste adhered to the edge of the release film 11 portion of the through hole 13 remains as it is. The phenomenon of so-called "pasting" occurs when the film is released together with the releasable film.
- the resistance value tends to increase, and the variation in the resistance value increases.
- the number of processed insulating substrates (prepredder sheets) 12 that can be filled with vias for a certain amount of paste decreases.
- productivity is deteriorated and cost requirements cannot be satisfied.
- the tendency of the resistance value to deteriorate due to the agglomeration degree exceeding 3.90 was remarkable because the smaller the via diameter of the through hole 13 was, the more easily the resistance was affected.
- the upper limit of the degree of aggregation of the conductive particles of the present invention is desirably 3.90 or less.
- the conductive particles according to Embodiment 2 were obtained by drying copper powder precipitated by a wet chemical reduction reaction, and had a cohesion degree of 1.41 without being subjected to pulverization treatment.
- An example using copper powder is shown in Example 3 of Table 1.
- the viscosity and conductor resistance of the conductive paste tend to depend on the degree of cohesion, and even if the crushed copper powder is subjected to the crushing treatment. There was a similar tendency as in the case without.
- controlling the degree of agglomeration without performing the pulverization treatment is not effective in controlling the coagulation degree, for example, in the case of a wet chemical reduction reaction, such as the reaction conditions such as the temperature, concentration, stirring state, and the temperature and temperature during drying. It is necessary to strictly control various conditions such as the amount of water absorption and the surface treatment agent for preventing aggregation. Therefore, the above-described method of externally applying energy to the aggregated particles to disintegrate the aggregated particles provides a simple, reliable, and inexpensive method for controlling the degree of aggregation. It is.
- the average particle size is preferably in the range of 0.5 to 20 tm, and the specific surface area is in the range of 0.07 to 1.7. m 2 / g is preferable.
- the average particle size is less than 0.5 Atm, the particle size is too small and the specific surface area becomes large, resulting in 1.7 m 2 / g, it becomes difficult to disperse the conductive particles in the binder at a high concentration.
- the average particle size exceeds 20 m, the number of conductive particles filled in one via hole decreases, and as a result, the chance of contact between conductive particles and the contact area decreases, so that the substrate resistance value decreases. Invite a rise.
- the specific surface area is 0. 0 7 m 2 / that is less than g and average particle size of the conductive particles and less 2 0 m is difficult, 1. 7 m 2 / g by weight, the conductive paste Bok of Since the viscosity is significantly increased, it is difficult to disperse the conductive particles at a high concentration.
- FIGS. 4A and 4B are diagrams showing one example of the particle size distribution of the copper powder according to the third embodiment, and each diagram represents the same sample.
- the copper powder used in the third embodiment is almost the same as that described in the second embodiment in the manufacturing method.
- As a method of improving the dispersibility of the conductive paste two or more different particle diameters have peaks.
- the conductive particles 3 used in the third embodiment have an average particle size of 0.2 to "! 0 m and a particle size having two or more peaks at 0.6 to 20 ⁇ m. If it exceeds the above range, the average particle size of the conductive particles is 0.5 to 20 m, and the specific surface area is 0.07 to 1.0.
- FIG.4B1 and FIG.4B2 show a particle size distribution measurement chart measured with a microtrack that is a wet type laser diffraction / scattering type as a particle size distribution measuring device.
- the frequency when particles are classified by particle size is plotted on the left vertical axis. It shows a frequency distribution.
- the peak of the particle size distribution referred to here is a mountain-like portion that becomes the mode in a certain particle size range of the frequency distribution.
- the part surrounded by a circle ( ⁇ ) corresponds to the peak.
- the first peak is around 1 m and the second peak is around 6 Atm.
- the average particle size of the conductive particles is the value of the particle size when the cumulative value of the frequency distribution becomes 50%, and the peak of the particle size distribution and the average particle size are used in different meanings.
- the particle size distribution was measured using the laser diffraction scattering method here, but other methods such as the electric resistance method represented by the Kohl-Counter and the image processing method are the same.
- two or more powders having different average particle size particle size distributions may be prepared and mixed using, for example, a V-type mixer. It is also possible to form three or more particle size distribution peaks by removing the intermediate particle size by classification. As a method that does not depend on mixing or classification, it is also possible to control the particle size during the reaction in, for example, a wet chemical reduction method. As another method, two or more nozzle injection ports may be provided in the atomization method to control the particle diameter. In any case, there is no particular limitation on the method of forming a peak in the particle size distribution.
- FI G.4B1 and FI G.4B2 are the particle size distributions of the conductive particles according to the third embodiment, which were measured with the above-mentioned wet laser diffraction scattering microtrack as a particle size distribution measuring device.
- the particle size distribution is shown.
- the first peak of the particle size distribution has a peak near 1 tm, and the second peak has a peak near 6 Atm. 5 wt% and 95 wt% are mixed, respectively. Copper powder.
- the average particle size is a value calculated from each frequency when the particles are classified according to the particle size, and refers to the particle size when the cumulative value is 50%.
- the average particle size of the powder obtained by mixing is greatly different.
- FI G. 4B is an example of measuring the particle size distribution of the same copper powder described above on a volume basis and a number basis.
- the average particle diameters (D 5 ) are 6.04 and 1.03, respectively.
- the particle size distribution of the conductive particles according to the conductive base of the present invention is characterized by having two or more peaks, and the calculation standard does not matter much. I want to go.
- a circuit-forming substrate was formed by the same manufacturing method as in Embodiment 2, and the peak value of the particle size distribution of the copper powder used for the conductive paste of the present invention, the viscosity of the conductive paste, and the conductivity of via holes were determined.
- the relationship with the transmission resistance will be described with reference to Table 2 and FIG.
- Viscosity is measured at R14 / 3 ° cone, 0.5rpm (Toki Sangyo RE-80U)
- Substrate resistance value is the average value of the series resistance value for 500 via holes (including wiring resistance 0.7 ⁇ ). Comparative Examples 3 and 4 in Table 2 have only one peak of the particle size distribution. And that the concentration was not controlled.
- the conductive particles according to the present invention two or more peaks as described above, for example, as shown in the schematic diagram of FIG. 4A, a relatively large peak corresponding to the second peak of the particle size distribution is obtained.
- a relatively small particle corresponding to the first peak of the particle size distribution enters between particles having a particle size, thereby suppressing aggregation of small particles or preventing small particles from being used for large particles.
- a function that enhances dispersibility by playing a role like "co-mouth” appears. In other words, powders having different particle sizes exhibit fluidity, which is effective in reducing viscosity.
- the mixing ratio can also be arbitrarily selected according to the via diameter of the through hole to be filled divided by the type and size of the conductive particles to be used.
- a pre-preductor as a pre-preductor, a nonwoven fabric of aramide fiber impregnated with epoxy resin (aramide Z epoxy) and a woven fabric of glass fiber impregnated with epoxy resin are used.
- the fibers Glass Z epoxy
- PBO poly paraphenylene benzobisazole
- PBI poly benzimidazole
- PBZT polyparaphenylene benzene
- thermosetting resin or thermoplastic resin such as polyimide resin, phenol resin, fluororesin, unsaturated polyester resin, PPE (polyphenylene ether) resin or cyanate ester resin
- conductive particles obtained by adding a surface treatment agent such as an organic fatty acid / silane silane agent for the purpose of dispersing or preventing the conductive particles to the conductive particles are also used as the conductive particles according to the conductive paste of the present invention. It is possible to do. Industrial applicability
- the present invention has an average particle size of 0.5 to 20 m, a specific surface area of 0.07 to 1.7 m 2 / g, and has a moderate
- the conductive particles in which the aggregates are formed it is possible to supply a conductive paste having excellent fluidity and dispersibility.
- the good fluidity and dispersibility of the conductive paste stabilizes the filling of the via and the contact between the conductive particles inside the via hole, and stably forms a high-quality via-hole conductor with little variation.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Manufacturing & Machinery (AREA)
- Conductive Materials (AREA)
- Printing Elements For Providing Electric Connections Between Printed Circuits (AREA)
- Parts Printed On Printed Circuit Boards (AREA)
Abstract
Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP04703883A EP1589540A4 (en) | 2003-01-23 | 2004-01-21 | CONDUCTIVE PASTE, METHOD FOR THE PRODUCTION THEREOF, CONDUCTOR PLATE WITH SUCH A CONDUCTIVE PASTE, AND METHOD FOR THE PRODUCTION THEREOF |
US10/509,755 US20050172483A1 (en) | 2003-01-23 | 2004-01-21 | Conductive paste, method for producing same, circuit board using such conductive paste and method for producing same |
Applications Claiming Priority (8)
Application Number | Priority Date | Filing Date | Title |
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JP2003-014556 | 2003-01-23 | ||
JP2003014553A JP4078990B2 (ja) | 2003-01-23 | 2003-01-23 | 導電性ペースト、その導電性ペーストを用いた回路形成基板、およびその製造方法 |
JP2003-014553 | 2003-01-23 | ||
JP2003014554A JP2004265607A (ja) | 2003-01-23 | 2003-01-23 | 導電性ペースト、その導電性ペーストを用いた回路形成基板、およびその製造方法 |
JP2003-014554 | 2003-01-23 | ||
JP2003014556A JP2004264031A (ja) | 2003-01-23 | 2003-01-23 | 導電性粒子の計測方法 |
JP2003-014555 | 2003-01-23 | ||
JP2003014555A JP4078991B2 (ja) | 2003-01-23 | 2003-01-23 | 導電性ペーストの製造方法 |
Publications (1)
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WO2004066316A1 true WO2004066316A1 (ja) | 2004-08-05 |
Family
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PCT/JP2004/000460 WO2004066316A1 (ja) | 2003-01-23 | 2004-01-21 | 導電性ペースト及びその製造方法並びにその導電性ペーストを用いた回路基板及びその製造方法 |
Country Status (4)
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US (1) | US20050172483A1 (ja) |
EP (1) | EP1589540A4 (ja) |
TW (1) | TWI325739B (ja) |
WO (1) | WO2004066316A1 (ja) |
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JP2005240092A (ja) * | 2004-02-26 | 2005-09-08 | Dowa Mining Co Ltd | 銀粉およびその製造方法 |
TW200833752A (en) * | 2006-10-23 | 2008-08-16 | Lord Corp | Highly filled polymer materials |
JP5217640B2 (ja) * | 2008-05-30 | 2013-06-19 | 富士通株式会社 | プリント配線板の製造方法およびプリント基板ユニットの製造方法 |
JP2009290135A (ja) * | 2008-05-30 | 2009-12-10 | Fujitsu Ltd | プリント配線板の製造方法および導電性接合剤 |
JP5217639B2 (ja) * | 2008-05-30 | 2013-06-19 | 富士通株式会社 | コア基板およびプリント配線板 |
JP2009290124A (ja) * | 2008-05-30 | 2009-12-10 | Fujitsu Ltd | プリント配線板 |
US8488271B2 (en) * | 2009-07-06 | 2013-07-16 | Samsung Electro-Mechanics Japan Advanced Technology Co., Ltd. | Adhesion structure and method using electrically conductive adhesive, disk drive device using the adhesion structure and method, and method for manufacturing the disk drive device |
JP4713682B1 (ja) | 2010-02-25 | 2011-06-29 | パナソニック株式会社 | 多層配線基板、及び多層配線基板の製造方法 |
JP4616927B1 (ja) | 2010-02-25 | 2011-01-19 | パナソニック株式会社 | 配線基板、配線基板の製造方法、及びビアペースト |
JP4917668B1 (ja) * | 2010-12-29 | 2012-04-18 | パナソニック株式会社 | 多層配線基板、多層配線基板の製造方法 |
JP2012209148A (ja) * | 2011-03-30 | 2012-10-25 | Sony Corp | 導電性粒子、導電性ペースト、及び、回路基板 |
JP5687175B2 (ja) * | 2011-11-28 | 2015-03-18 | 有限会社 ナプラ | 微細空間内に機能部分を形成する方法 |
TWI550643B (zh) * | 2012-03-30 | 2016-09-21 | Taiyo Holdings Co Ltd | Conductive paste and conductive circuit |
JP5510531B1 (ja) * | 2012-11-29 | 2014-06-04 | 住友金属鉱山株式会社 | 銀粉及び銀ペースト |
JP5500237B1 (ja) * | 2012-12-05 | 2014-05-21 | 住友金属鉱山株式会社 | 銀粉 |
JP5505535B1 (ja) * | 2012-12-07 | 2014-05-28 | 住友金属鉱山株式会社 | 銀粉 |
JP6258347B2 (ja) * | 2013-10-29 | 2018-01-10 | 京セラ株式会社 | 配線基板およびこれを用いた実装構造体 |
JP6766057B2 (ja) * | 2015-09-30 | 2020-10-07 | 住友電気工業株式会社 | 導電層形成用塗布液及び導電層の製造方法 |
JP7226531B2 (ja) * | 2019-04-24 | 2023-02-21 | 株式会社レゾナック | シリコン貫通電極を有する基板の製造方法、シリコン貫通電極を有する基板及びシリコン貫通電極形成用銅ペースト |
JP7004921B2 (ja) | 2019-04-26 | 2022-01-21 | 日亜化学工業株式会社 | 発光モジュールの製造方法及び発光モジュール |
KR20210121445A (ko) * | 2020-03-30 | 2021-10-08 | (주)포인트엔지니어링 | 양극산화막 구조체 |
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Publication number | Publication date |
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TW200420204A (en) | 2004-10-01 |
EP1589540A4 (en) | 2009-01-28 |
EP1589540A1 (en) | 2005-10-26 |
TWI325739B (en) | 2010-06-01 |
US20050172483A1 (en) | 2005-08-11 |
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