EP3031551A1 - Verbundkupferpartikel und herstellungsverfahren dafür - Google Patents

Verbundkupferpartikel und herstellungsverfahren dafür Download PDF

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Publication number
EP3031551A1
EP3031551A1 EP14834408.8A EP14834408A EP3031551A1 EP 3031551 A1 EP3031551 A1 EP 3031551A1 EP 14834408 A EP14834408 A EP 14834408A EP 3031551 A1 EP3031551 A1 EP 3031551A1
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EP
European Patent Office
Prior art keywords
copper
particle
particles
inorganic oxide
composite
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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.)
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EP14834408.8A
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English (en)
French (fr)
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EP3031551A4 (de
Inventor
Toshihiro Kohira
Nobuhiro Sasaki
Hikaru Minowa
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.)
Mitsui Mining and Smelting Co Ltd
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Mitsui Mining and Smelting Co Ltd
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Publication of EP3031551A1 publication Critical patent/EP3031551A1/de
Publication of EP3031551A4 publication Critical patent/EP3031551A4/de
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/20Conductive material dispersed in non-conductive organic material
    • H01B1/22Conductive material dispersed in non-conductive organic material the conductive material comprising metals or alloys
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/06Metallic powder characterised by the shape of the particles
    • B22F1/068Flake-like particles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/16Metallic particles coated with a non-metal
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C9/00Alloys based on copper
    • C22C9/01Alloys based on copper with aluminium as the next major constituent
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/14Conductive material dispersed in non-conductive inorganic material
    • H01B1/16Conductive material dispersed in non-conductive inorganic material the conductive material comprising metals or alloys
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C9/00Alloys based on copper

Definitions

  • This invention relates to a composite copper particle and a process for producing the same.
  • Flake-like copper particles have a large specific surface area and a large contact area between themselves due to their flatness. Therefore, addition of flake-like copper particles to an electroconductive composition improves electric conductivity and allows for viscosity adjustment.
  • the assignee common to this patent application proposes a flake-like copper powder and a conductive paste containing the flake-like copper powder (see Patent Literature 1).
  • Patent Literature 1 discloses a flake-like copper powder having a particle diameter of 10 ⁇ m or less, an SD/D 50 of 0.5 or less (wherein SD is a standard deviation of particle size distribution, and D 50 is a particle diameter at 50% in the cumulative weight-based distribution), and a D 90 /D 10 of 4.0 or less (wherein D 90 is a particle diameter at 90% in the cumulative weight-based distribution, and D 10 is a particle diameter at 10% in the cumulative weight-based distribution).
  • Patent Literature 1 also discloses a flake-like copper powder having a particle diameter of 10 ⁇ m or less, an SD/D 50 of 0.15 to 0.35, and an aspect ratio ([thickness]/[D 50 ] of 0.3 to 0.7.
  • the flake-like copper powder described in Patent Literature 1 allows for forming a fine electrical circuit.
  • Patent Literature 1 JP 2003-119501A
  • An object of the invention is to provide composite copper particles free from the various disadvantages of the aforementioned conventional techniques and a process for making the same.
  • the present invention provides a composite copper particle including a flake-like copper particle and a plurality of inorganic oxide particles which are finer than the flake-like copper particle, the inorganic oxide particles being unevenly distributed on a surface of the flake-like copper particle.
  • the present invention provides a process for producing composite copper particles comprising subjecting a mixed powder of a starting spherical copper powder and a particulate inorganic oxide to a dispersion process using beads thereby plastically flattening the copper particles of the starting copper powder and locating the particulate inorganic oxide on the surface of the flattened copper particles, the particulate inorganic oxide powder having a ratio of a volume cumulative particle diameter D 50 (nm) measured by a dynamic light scattering method to a particle size D BET calculated from its BET specific surface area, D 50 /D BET , of 60 or greater.
  • the composite copper particle of the invention is composed of a copper particle as a matrix and a plurality of inorganic oxide particles combined with the matrix.
  • the copper particle as a matrix is a flake-like copper particle having a flat shape, and the inorganic oxide particles are finer than the flake-like copper particles as a matrix.
  • the composite copper particle of the invention is characterized by the fashion of the inorganic oxide particles being combined with the flake-like matrix copper particle. Specifically, the inorganic oxide particles are unevenly distributed on the surface of the flake-like copper particle. When described as being unevenly distributed on the surface, the inorganic oxide particles are not uniformly distributed on the entire surface of the flake-like copper particle but exist in part of the surface. Thus, the surface of the flake-like copper particle has an area where the inorganic oxide particles are present (hereinafter “composite area”) and an area where the inorganic oxide particles are substantially absent (hereinafter “composite-free area"). When the inorganic oxide particles are unevenly distributed on the surface of the flake-like copper particle, the following advantage is obtained.
  • a coating film of a conductive composition such as a conductive paste, prepared using the composite copper particles of the invention is fired to form, e.g., an electronic circuit
  • the composite areas, where the inorganic oxide particles are present, of the composite copper particles are less likely to bind together than the composite-free areas.
  • the sites at which the composite copper particles are less likely to bind together provide passageways for escape of the gas generated during firing.
  • blistering of an electrode that might occur during firing is prevented effectively, whereby the electronic circuit and the like formed by using the composite copper particles of the invention will be prevented from increasing electric resistivity and have improved surface smoothness.
  • flake-like copper particles having no inorganic oxide particles on their surface are liable to bind together on their flat surfaces, failing to provide a passageway for escape of the gas, which can result in blistering of the electrode during firing.
  • inorganic oxide particles are described as being unevenly distributed, it means that both a composite area and a composite-free area are observed on the outer peripheral surface of a composite copper particle of the invention when the composite copper particle is ultramicrotomed into sections and the sections are subjected to elemental mapping as shown in Figs. 1 through 3 .
  • the entire peripheral surface of a composite copper particle is found to be a composite area or, conversely, a composite-free area, the inorganic oxide particles are not described as being unevenly distributed.
  • a plurality of inorganic oxide particles be agglomerated into agglomerates as shown in Fig. 2 as will be described later.
  • the inorganic oxide particles are located on the surface of a flake-like copper particle through an anchor effect in such a fashion that, for example, part of an inorganic oxide particle is embedded into the surface of the flake-like copper particle.
  • the inorganic oxide particles are located on the surface of a flake-like copper particle through the cohesive force (surface energy) produced between the inorganic oxide particle and the flake-like copper particle.
  • a plurality of the inorganic oxide particles are agglomerated by the surface energy generated between the inorganic oxide particles.
  • the composite copper particles of the invention having the inorganic oxide particles distributed unevenly on the surface of a flake-like copper particle can be produced by, for example, the process described infra.
  • the effect of unevenly distributing the inorganic oxide particles on the surface of a flake-like copper particle can be enhanced when the proportion of the inorganic oxide particles in the composite copper particles of the invention ranges from 0.001 mass% to 5.0 mass%, preferably 0.01 mass% to 3.0 mass%, more preferably 0.01 mass% to 2.0 mass%.
  • the proportion of the inorganic oxide particles is measured by, for example, inductively coupled plasma-atomic emission spectrometry (ICP-AES).
  • the inorganic oxide particles are only necessary for the inorganic oxide particles to be localized only on the surface of a flake-like copper particle.
  • the inorganic oxide particles do not need to be present inside the flake-like copper particle, which does not mean to exclude the presence of the inorganic oxide particle inside the flake-like copper particle. Nevertheless, the smaller the ratio of the inorganic oxide particles present inside the flake-like copper particle, the better for making the effect of the uneven distribution of the inorganic oxide particles more pronounced. From this standpoint, the ratio of the inorganic oxide particles present inside the flake-like copper particles to the total content of the inorganic oxide particles of the composite copper particles of the invention is preferably 1.0 mass% or less, more preferably 0.7 mass% or less.
  • This ratio can be measured by, for example, elemental mapping of a section of a composite copper particle of the invention.
  • an inorganic oxide particle present inside a flake-like copper particle denotes an inorganic oxide particle that is not at all exposed on the surface of the composite copper particle of the invention.
  • the composite copper particles of the invention have a flaky shape reflecting the shape of the flake-like copper particles as a matrix.
  • the flakiness of the composite copper particles of the invention can be represented by an "aspect ratio" of the maximum diameter d of a plane of the composite copper particle to the maximum thickness t of the composite copper particle, d/t.
  • the aspect ratio d/t of the composite copper particles is preferably 5 to 30, more preferably 5 to 25, even more preferably 7 to 20.
  • An electronic circuit and the like formed by using the composite copper particles with such flakiness exhibit increased denseness and are effectively prevented from increasing electrical resistance.
  • the aspect ratio of the composite copper particles is obtained by measuring the maximum diameter d of the plane of the particle and the thickness t of the particle. Specifically, particle are photographed using a scanning electron microscope (SEM), and the ratio of the maximum diameters d of the plane of the particle to the thicknesses t of the particle of the micrograph is calculated.
  • SEM scanning electron microscope
  • the composite copper particles of the invention are not only flake-like but microfine.
  • flaky and microfine composite copper particles of the invention provides an electronic circuit and the like with further increased denseness and further ensured prevention from an increase of electrical resistance.
  • the composite copper particles of the invention preferably have a volume cumulative particle diameter D 50 at a cumulative volume of 50 vol% as measured by a laser diffraction scattering method of 0.1 ⁇ m to 10 ⁇ m, more preferably 0.2 ⁇ m to 9.0 ⁇ m, even more preferably 0.3 ⁇ m to 7.0 ⁇ m.
  • Copper particles tend to have a reduced sintering onset temperature with a decrease in particle size. This tendency also applies to the composite copper particles of the invention. Reduction in sintering onset temperature is undesirable for some applications of the composite copper particles of the invention.
  • the composite copper particles of the invention are protected from reduction of the sintering onset temperature by virtue of the presence of the inorganic oxide particles on the surface of the flake-like matrix copper particles. That is, although the composite copper particles of the invention are microfine particles, the composite copper particles of the invention has approximately the same sintering onset temperature as conventionally used copper particles.
  • the composite copper particles of the invention are flake-like and have a broad particle size distribution.
  • An electronic circuit and the like formed by using the composite copper particles that have a flaky shape with a broad size distribution exhibit increased denseness and are thereby effectively prevented from increasing in electrical resistance.
  • a ratio of the maximum diameter D max to D 50 , D max /D 50 provides a parameter showing the breadth of the particle size distribution, wherein D max is measured by a laser diffraction scattering method, and D 50 is measure by a laser diffraction scattering method.
  • the composite copper particles of the invention preferably have a D max /D 50 of 3 to 10, more preferably 3 to 9, even more preferably 3 to 8.
  • the composite copper particles of the invention which have the above-described particle size distribution can be obtained by properly selecting the conditions in the step of flattening starting copper particles in the hereinafter described preferred process for producing the composite copper particle of the invention.
  • the size of the flake-like copper particles as a matrix of the composite copper particles of the invention is equal to that of the composite copper particles of the invention.
  • the size of the inorganic oxide particles as calculated from their BET specific surface area (hereinafter referred to as BET particle size) is preferably 1 nm to 500 nm, more preferably 1 nm to 400 nm, even more preferably 1 nm to 300 nm, provided that it is smaller than the size of the flake-like copper particles.
  • the BET specific surface area of the inorganic oxide particles, from which the BET particle size is calculated, is measured by, for example, a gas adsorption method in which the specific surface area of particles is calculated from the amount of gas adsorbed on the surface of the particles.
  • a gas adsorption method in which the specific surface area of particles is calculated from the amount of gas adsorbed on the surface of the particles.
  • MonoSorb from Yuasa Ionics Co., Ltd. may be used as a measuring instrument.
  • the inorganic oxide particles that can be used in the invention preferably have higher hardness than copper so that the inorganic oxide particles may easily be located on the surface of the flake-like copper particles in the hereinafter described preferred method for producing the composite copper particles of the invention.
  • hardness denotes a hardness measured with a Mohs hardness meter.
  • preferred materials of the inorganic oxide particles include alumina, zirconia, silica, barium titanate, yttrium oxide, and zinc oxide. These materials may be used either individually or in combination of two or more thereof.
  • the flake-like copper particle as a matrix to be combined with the inorganic oxide particles may be made solely of copper or may comprise at least one other metal element or semimetal element (hereinafter inclusively referred to as a metallic element for the sake of simplicity) in addition to copper.
  • a metallic element for the sake of simplicity
  • the other metallic elements if used in combination with copper include those that behave differently from copper during sintering, such as aluminum, zirconium, yttrium, and silicon. These metallic elements may be used either individually or in combination of two or more thereof. The inclusion of such a metallic element in the flake-like copper particle makes it possible to control the behavior of copper during sintering.
  • the other metallic element included in the flake-like copper particle may be present in the form of an elemental metal, an alloy with copper, or a compound (e.g., an oxide). To ensure the effect described above, it is preferred that the other metallic element be present in the flake-like copper particle in the form of a compound, such as an oxide.
  • the other metallic element may be evenly distributed in the flake-like copper particle or localized at specific sites. As a result of the inventor's study, it has been revealed to be desirable that the other metallic element be localized in the surface portion of the flake-like copper particles. This is because, the inventor considers, the vicinities of the surface are influential on the sintering behavior.
  • the metallic element When the other metallic element is localized on the surface of the flake-like copper particle, it is preferred for the metallic element to be uniformly distributed over the entire surface of the flake-like copper particle, so that the sintering behavior during firing is controlled easily.
  • the ease of sintering behavior control combined with the broad particle size distribution of the flake-like copper particles makes electrode thickness design easier.
  • the content of the other metallic element is preferably 0.001 mass% to 5.0 mass%, more preferably 0.01 mass% to 3.0 mass%, even more preferably 0.05 mass% to 1.0 mass%, based on the mass of copper in the flake-like copper particles.
  • the other metallic element When the other metallic element is present in that ratio, the other metallic element produces a more pronounced effect.
  • a mixed powder of a starting, spherical copper powder and an inorganic oxide powder is subjected to a dispersion process using beads.
  • the copper particles are plastically flattened, and the inorganic oxide particles are located on the surface of the flattened copper particles.
  • What is important in this operation is to use inorganic oxide powder having a high degree of agglomeration. While being combined with the spherical copper powder, a highly agglomerated inorganic oxide powder can be localized unevenly.
  • an inorganic oxide powder having a D 50 /D BET of 60 or greater, where D 50 is a volume cumulative particle diameter (nm) at a cumulative volume of 50 vol% as measured by a dynamic light scattering method, and D BET is a BET particle size calculated from BET specific surface area of the particulate inorganic oxide powder.
  • the D 50 /D BET value is an index representing the degree of agglomeration. A greater D 50 /D BET value means a higher degree of agglomeration.
  • the agglomerated state of an inorganic oxide powder having a D 50 /D BET of 60 or greater will be reflected on the resulting composite copper particles such that the inorganic oxide particles will unevenly be distributed on the surface of the flake-like copper particle.
  • the D 50 /D BET of the inorganic oxide particles is desirably as high as possible.
  • the D 50 /D BET is preferably 60 to 300, more preferably 60 to 100.
  • the beads used to subject the mixed powder of the spherical copper powder and the inorganic oxide powder to a dispersion process preferably have a diameter of 0.005 to 1.0 mm, more preferably 0.05 to 0.5 mm, even more preferably 0.05 to 0.3 mm.
  • the beads may be of any material that is harder than copper and the inorganic oxide particles, such as alumina, zirconia, or silica.
  • the amount of the beads to be used is preferably 50 mass% to 90 mass%, more preferably 60 mass% to 85 mass%, even more preferably 65 mass% to 85 mass%, relative to the capacity of the device used to carry out the process.
  • the dispersion process using beads may be carried out, for example, by means of a bead mill.
  • the time required for the dispersion process varies mainly according to the capacity of the device.
  • the time required for treating 1 kg of copper powder using a bead mill having a capacity of 0.1 liters to 300 liters is preferably 5 minutes to 90 minutes, more preferably 10 minutes to 70 minutes.
  • the starting spherical copper powder is successfully flattened while retaining to some extent the agglomerated state of the inorganic oxide powder, and the agglomerated inorganic oxide powder can be fixedly located on the surface of the flattened, flake-like copper particles.
  • the inorganic oxide particles do not change in particle size (primary particle diameter) between before and after being combined with the flattened copper powder. Therefore, the particle size of the inorganic oxide powder used as a raw material is equal to that of the inorganic oxide particles contained in the composite copper particles of the invention.
  • the starting copper particles used as a raw material are flattened by the dispersion process using beads, i.e., they change in shape and size between before and after being combined.
  • the starting copper powder before the dispersion process is an aggregate of spherical copper particles.
  • the starting copper powder has the volume cumulative particle diameter D 50 at a cumulative volume of 50 vol% as measured by a laser diffraction scattering method of preferably 0.03 ⁇ m to 8 ⁇ m, more preferably 0.05 ⁇ m to 7 ⁇ m, for ease of obtaining microfine composite copper particles.
  • a laser diffraction scattering method preferably 0.03 ⁇ m to 8 ⁇ m, more preferably 0.05 ⁇ m to 7 ⁇ m, for ease of obtaining microfine composite copper particles.
  • copper particles other than spherical copper particles there may be a difficulty in obtaining composite copper particles having a desired flaky shape. Additionally, spherical copper particles are easier to produce than otherwise shaped copper particles.
  • the starting copper powder preferably has a high degree of agglomeration thereby to provide composite copper particles having a high degree of agglomeration.
  • the starting copper powder has a ratio of the maximum diameter D max to D 50 , D max /D 50 , of preferably 2 to 15, more preferably 3 to 13, even more preferably 3 to 10, wherein D max and D 50 are measured by a laser diffraction scattering method.
  • a starting copper powder having such a particle size distribution can be prepared by properly selecting the conditions for the preparation by, for example, a dry process (e.g., atomizing) or a wet reduction process. Otherwise, copper powders prepared by these processes may be mixed or classified to obtain powder having a desired particle size distribution.
  • a metallic element other than copper is included into the desired composite copper particles
  • aluminum may be incorporated as follows. In a dry process, aluminum is added to molten copper. In a wet process, an oxide of aluminum, such as alumina, is added in the course of copper reduction. In the thus prepared starting copper particles, aluminum element is chiefly present close to the surface of the particles.
  • a conductive paste may include the composite copper particles of the invention, an organic vehicle, and a glass frit.
  • the organic vehicle comprises a resin component and a solvent.
  • the resin component are acrylic resins, epoxy resins, ethyl cellulose, and carboxyethyl cellulose.
  • the solvent include terpene solvents, such as terpineol and dihydroterpineol, and ether solvents, such as ethyl carbitol and butyl carbitol.
  • the glass frit examples include borosilicate glass, barium borosilicate glass, and zinc borosilicate glass.
  • the amount of the aggregate of microfine particles in the conductive paste are preferably 36 to 97.5 mass%.
  • the amount of the glass frit in the conductive paste 1.5 to 14 mass%.
  • the amount of the organic vehicle in the conductive paste 1 to 50 mass%.
  • the conductive component in the conductive paste may consist solely of the composite copper particles of the invention or a mixture of the aggregate of microfine particles and other fine copper particle. In the latter case, the viscosity of the paste can be adjusted more accurately.
  • CB-3000 available from Mitsui Mining & Smelting Co., Ltd. was used as a starting copper powder.
  • CB-3000 had a D max /D 50 of 3.5 and a D 50 of 3.2 ⁇ m.
  • the D 50 and D max were measured using Microtrac X-100 from Nikkiso Co., Ltd.
  • the starting copper powder contained 0.25% aluminum. Aluminum existed in the form of a simple substance both at and in the vicinity of the surface of the particles.
  • Zirconia powder was used as an inorganic oxide powder.
  • the powder had a D 50 /D BET of 70 and a BET particle size D BET of 15 nm.
  • the D 50 was measured using Zeta Sizer ZS available from Malvern.
  • the D BET was measured using MonoSorb available from Yuasa Ionics.
  • a thousand grams of the starting copper powder and 100 g of the inorganic oxide powder were put in a 2 liter-bead mill and mixed. Then, Zirconia beads with a diameter of 0.2 mm were put into the mill to carry out a dispersion process for 20 minutes to obtain composite copper particles as desired. The amount of the beads was 70% of the capacity of the bead mill. The proportion of the inorganic oxide particles in the composite copper particles was found to be 0.5% as measured by the method described supra.
  • the resulting composite copper powder was ultramicrotomed into sections, and the sections were subjected to elemental mapping by scanning transmission electron microscopy-energy dispersive spectroscopy (STEM-EDS) for copper, zirconium, and aluminum.
  • STEM-EDS scanning transmission electron microscopy-energy dispersive spectroscopy
  • the composite copper particles are flake-like, and zirconia particles are unevenly distributed over their surface.
  • a plurality of the zirconia particles are agglomerated to form zirconia agglomerates.
  • the aluminum is present not inside but in the surface portion of the flake-like copper particles.
  • Composite copper particles were obtained in the same manner as in Example 1, except for replacing the zirconia powder used in Example 1 with alumina powder.
  • the alumina powder had a D 50 /D BET of 60 and a BET particle size D BET of 10 nm.
  • the proportion of the inorganic oxide particles in the resulting composite copper particles was found to be 0.5% as determined by the method described above.
  • Composite copper particles were obtained in the same manner as in Example 2, except for replacing the starting copper power described in Example 1 with a starting copper powder having a D max /D 50 of 2.5 and a D 50 of 3.3 ⁇ m.
  • the starting copper powder contained 0.13% aluminum.
  • the elemental aluminum existed both at and in the vicinity of the surface of the particle.
  • the proportion of the inorganic oxide particles in the composite copper particles was found to be 0.5% as determined by the method described above.
  • Flake-like copper particles were obtained in the same manner as in Example 1, except that the treatment in a bead mill was performed without adding zirconia powder.
  • Flake-like copper particles were obtained in the same manner as in Example 3, except that the treatment in a bead mill was performed without adding alumina powder.
  • thermomechanical analysis TMA
  • TMA/SS6300 available from Seiko Instruments.
  • TMA thermomechanical analysis
  • a rate of temperature rise of 10°C/min The results obtained are shown in Fig. 4 .
  • the composite copper particles obtained in Examples have a thermal shrinkage onset temperature, i.e., a sintering onset temperature, equal to or higher than that of the copper particles of Comparative Examples.
  • a conductive paste was prepared using the copper particles obtained in Examples and Comparative Examples.
  • the conductive paste comprised 70% of the copper particles, 25% of terpineol, and 5% of ethyl cellulose.
  • the conductive paste was applied to an alumina substrate using an applicator to form a 20 ⁇ m thick coating film, which was fired in a nitrogen atmosphere at 800°C for 1 hour.
  • the surface condition of the thus formed conductive film (electrode) was observed with the naked eye to evaluate continuity of the electrode. When the electrode had continuity, the electrode was evaluated as "yes", and when the electrode did not have continuity, the electrode was evaluated as "no". The results were shown in Table 1.
  • the invention provides composite copper particles the sintering temperature of which is approximately the same as those of conventionally used copper powders and which are capable of making an electrode with reduced occurrence of blistering.
  • the invention also provides a process for producing the composite copper particles.

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  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Nanotechnology (AREA)
  • Metallurgy (AREA)
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EP14834408.8A 2013-08-07 2014-08-01 Verbundkupferpartikel und herstellungsverfahren dafür Withdrawn EP3031551A4 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2013164445A JP2015034309A (ja) 2013-08-07 2013-08-07 複合銅粒子及びその製造方法
PCT/JP2014/070346 WO2015019959A1 (ja) 2013-08-07 2014-08-01 複合銅粒子及びその製造方法

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EP3031551A1 true EP3031551A1 (de) 2016-06-15
EP3031551A4 EP3031551A4 (de) 2017-04-26

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JP (1) JP2015034309A (de)
KR (1) KR20160040538A (de)
CN (1) CN105451914A (de)
TW (1) TWI556257B (de)
WO (1) WO2015019959A1 (de)

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CN105451914A (zh) 2016-03-30
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WO2015019959A1 (ja) 2015-02-12
EP3031551A4 (de) 2017-04-26
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