WO2006126564A1 - 鉛フリーソルダペースト - Google Patents
鉛フリーソルダペースト Download PDFInfo
- Publication number
- WO2006126564A1 WO2006126564A1 PCT/JP2006/310307 JP2006310307W WO2006126564A1 WO 2006126564 A1 WO2006126564 A1 WO 2006126564A1 JP 2006310307 W JP2006310307 W JP 2006310307W WO 2006126564 A1 WO2006126564 A1 WO 2006126564A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- solder
- lead
- powder
- nanoparticles
- flux
- Prior art date
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
- B23K35/22—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
- B23K35/24—Selection of soldering or welding materials proper
- B23K35/26—Selection of soldering or welding materials proper with the principal constituent melting at less than 400 degrees C
- B23K35/262—Sn as the principal constituent
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K1/00—Soldering, e.g. brazing, or unsoldering
- B23K1/0008—Soldering, e.g. brazing, or unsoldering specially adapted for particular articles or work
- B23K1/0016—Brazing of electronic components
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
- B23K35/02—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by mechanical features, e.g. shape
- B23K35/0222—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by mechanical features, e.g. shape for use in soldering, brazing
- B23K35/0244—Powders, particles or spheres; Preforms made therefrom
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
- B23K35/02—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by mechanical features, e.g. shape
- B23K35/0222—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by mechanical features, e.g. shape for use in soldering, brazing
- B23K35/0244—Powders, particles or spheres; Preforms made therefrom
- B23K35/025—Pastes, creams, slurries
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
- B23K35/22—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
- B23K35/22—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
- B23K35/36—Selection of non-metallic compositions, e.g. coatings, fluxes; Selection of soldering or welding materials, conjoint with selection of non-metallic compositions, both selections being of interest
- B23K35/362—Selection of compositions of fluxes
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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
- H05K3/30—Assembling printed circuits with electric components, e.g. with resistor
- H05K3/32—Assembling printed circuits with electric components, e.g. with resistor electrically connecting electric components or wires to printed circuits
- H05K3/34—Assembling printed circuits with electric components, e.g. with resistor electrically connecting electric components or wires to printed circuits by soldering
- H05K3/3457—Solder materials or compositions; Methods of application thereof
- H05K3/3485—Applying solder paste, slurry or powder
-
- 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
- H05K2201/0206—Materials
- H05K2201/0215—Metallic fillers
-
- 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
- H05K2201/0242—Shape of an individual particle
- H05K2201/0257—Nanoparticles
Definitions
- the present invention relates to a solder paste used for soldering electronic equipment, and more particularly to a Sn—Zn-based lead-free solder paste.
- a method for soldering electronic components there are a brazing method, a flow method, a reflow method, and the like.
- solder paste with solder powder and flux power is applied only to the necessary parts of the printed circuit board by printing or discharging, and electronic parts are mounted on the application part, and then soldered with a heating device such as a reflow furnace.
- a heating device such as a reflow furnace.
- This is a method of melting the paste and soldering the electronic component and printed circuit board.
- This reflow method is capable of soldering a large number of locations in a single operation, and it can be applied to narrow pitch electronic components. In addition, no bridging occurs and solder does not adhere to unnecessary locations. It can perform soldering with excellent reliability.
- the solder paste used in the conventional reflow method has a solder powder of Pb—Sn alloy.
- This Pb-Sn alloy has a melting point of 183 ° C in its eutectic composition (Pb-63Sn) and has little heat effect or excellent solderability even for electronic components that are vulnerable to heat. This means that there are few occurrences of soldering defects such as dewetting.
- soldering defects such as dewetting.
- solder is attached to the copper foil of the printed circuit board, and the copper foil and the solder are separated. This is because it cannot be reused.
- acid rain comes into contact with this landfilled printed circuit board, Pb in the solder elutes and contaminates groundwater.
- Pb poisoning will occur if people and livestock drink Pb-containing groundwater for many years. Therefore, there is a strong demand for the so-called “lead-free solder” that does not contain Pb in the electronic equipment industry.
- Lead-free solder is based on Sn, and currently used lead-free solder is Sn-3.5Ag (melting point: 221 ° C), Sn-0.7Cu (melting point: 227 ° C), Sn-9Zn (melting point: 199 ° C), Sn-58 Bi (melting point: 139.C) and other binary alloys, Ag, Cu, Zn, Bi ⁇ In, Sb, Ni (3) A third element such as Cr, Co, Fe, Mn, P, Ge, or Ga is added as appropriate.
- the “system” in the present invention is an alloy itself or an alloy to which one or more third elements are added based on a binary alloy.
- Sn-Zn alloy is Sn-Zn alloy itself, or an alloy with one or more of the above-mentioned third elements added to Sn-Zn.
- Sn-Ag alloy is Sn-Ag alloy itself or Sn_Ag. It is an alloy containing one or more of the aforementioned third elements.
- the Sn-Ag, Sn-Cu, and Sn-Ag-Cu lead-free solders that are widely used at present have a melting point of 220 ° C or higher, so when used as a solder paste for the reflow method , The peak temperature of the reflow was over 250 ° C! /, And there was a problem that the electronic parts and the printed circuit board were thermally damaged.
- Sn-Zn lead-free solder is close to the melting point of conventional Pb-Sn eutectic solder.
- Sn-9Zn eutectic lead-free solder has a melting point of 199 ° C, -Can be used with reflow profile of Sn eutectic solder. Therefore, there is little thermal effect on electronic components and printed circuit boards.
- Sn-9Zn eutectic solder paste has poor wettability, so many Sn-8Zn-3Bi lead-free solder pastes with Bi added to alloys near Sn-Zn eutectic are used. Yes.
- Sn-Zn-based lead-free solders have a melting point close to that of conventional Sn-Pb and use Zn, which is an essential ingredient for humans. Therefore, compared to other lead-free solders, Zn is superior to other lead-free solders in that it has more reserves on the earth and is cheaper than In, Ag, Bi, etc. For this reason, it is used as a solder paste for solder paste, especially for Sn-Ag lead-free solder, because it does not have the heat resistance of the parts, so it cannot be used.
- solder in which a metal powder containing Group 1B as a constituent element dispersed in a flux is mixed with Sn-Zn lead-free solder.
- a paste Japanese Patent Laid-Open No. 2002-224880
- a lead-free solder alloy in which Ag is added to a Sn-Zn lead-free solder Japanese Patent Laid-Open No. 9-253882
- Nanoparticles are powders with a particle size on the order of nm, and they intervene between powders with a particle size of the conventional / zm order and exhibit various characteristics.
- N-particles are arranged on the surface of the solder spherical particles to improve the fracture resistance (Japanese Patent Publication No. 2003-062687), and Sn_Zn lead-free solder is self-organized.
- a soldered nanoparticle solder alloy Japanese Patent Laid-Open No. 2004-268065 is disclosed.
- Patent Document 1 JP 2002-224880 A
- Patent Document 2 Japanese Patent Laid-Open No. 9-253882
- Patent Document 3 Japanese Patent Laid-Open No. 2003-062687
- Patent Document 4 Japanese Patent Laid-Open No. 2004-268065
- the Group 1B metal powder added to the Sn-Zn lead-free solder powder is more than 10% of the Sn-Zn lead-free solder powder, raising the peak temperature of reflow. Otherwise, the solder will not melt, and if it can be reflowed with almost the same temperature profile as the conventional Sn-Pb solder! /, The advantage of Sn-Zn lead-free solder will be lost. Furthermore, when a single group 1B metal powder is used, the metal powder does not dissolve in a general reflow profile, and the powder remains as particles in the molten solder.
- the Group 1B metal particles present in the solder improve the metal strength at room temperature, but in an environment that is repeatedly exposed to high and low temperatures, the molten Sn-Zn lead-free solder and the Group 1B metal particles in the solder Therefore, metal fatigue occurs inside the solder, causing a decrease in the strength of the solder.
- Patent Document 2 when Ag is added to a Sn-Zn lead-free solder alloy, the metal strength of the Sn-Zn lead-free solder alloy is improved. You have to do more.
- the present inventor has developed a fine solder structure after solidification by attaching nanoparticles containing one or more types of Ag Au and Cu to the Sn-Zn-based lead-free solder powder surface with a particle size of 5 300 nm.
- the present invention has been completed by finding that it is possible to obtain a molten joint that does not decrease the joint strength even when exposed to an environment of high temperature and high humidity.
- the present inventors can disperse 5 300 nanoparticles with a particle size of at least one kind of Ag, Au, and Cu in the flux, thereby fusing the solder and these nanoparticles during soldering mounting using the flux.
- the present invention was completed by finding that a solder joint with high joint strength after mounting can be obtained by miniaturizing the structure of the soldered portion. [0013] As a result of investigating the cause of the decrease in the strength of the soldered portion of Cu soldered with n-Zn lead-free solder, the present inventors have found that Cu-Zn is easily oxidized at the interface between copper and solder. It was found that this was due to the formation of an alloy layer.
- Sn-Pb solder Sn-Ag lead-free solder and Sn-Bi lead-free solder are soldered with Cu, Sn and Cu in the solder react to form an Sn-Cu alloy layer To do.
- Cu is soldered with Sn-Zn lead-free solder, a Cu-Zn alloy layer is formed.
- the Cu-Zn alloy layer is exposed to the outside of the fillet base just inside the fillet formed of solder! /
- the water adheres to the solder the water becomes electrolyte and the Zn in the solder is selectively It is oxidized and ionized.
- the oxidized Zn ions move to the Cu-Zn alloy layer to become a Cu-Zn alloy, and further the Zn ions move to the Cu portion through the alloy layer. And, in the Sn-Zn lead-free solder after the movement of Zn ions, voids of Zn removal occur. This phenomenon occurs when the voids generated at the Cu-Zn alloy layer interface gradually move along the interface, reducing the strength of the soldered area. Finally, it peels off at the bonding interface.
- the mechanism of refinement of the solder structure after soldering as inferred by the present inventor is as follows. 1. Ag Au and Cu nanoparticles have a particle size of about 5 300 nm. Due to the fineness of the particle size, they are evenly dispersed in a solvent such as ethanol and hardly precipitate. In other words, these nanoparticles can be treated as liquids in appearance, and even if they remain in a solid state at a reflow temperature below the melting temperature of the nanoparticles, the solderability by solder paste is adversely affected. N / A!
- Part of the core of the generated intermetallic compound is not completely dissolved in the part that dissolves in the liquid phase and the Sn-Zn lead-free solder during the reflow process. It is present in the liquid phase as a reaction of the components in the alloy.
- the Sn-Zn lead-free solder When the Sn-Zn lead-free solder is cooled, it reacts with these Zn and disperses in the liquid phase, and the nanoclusters become nuclei, increasing the number of Zn crystallization sites, resulting in Zn crystals. The output size is reduced.
- the solder paste of the present invention there are many in the melted solder as the core S of the intermetallic compound, so the refinement of Zn reaches the inner part of the solder not only on the outer surface of the solder, but the entire joint part Refined.
- the lead-free solder of the present invention has a solidus temperature due to alloying with Zn on the Zn-rich side where Ag Au, Cu, etc. react with Zn and have a large solid solubility with respect to Zn. It can only be obtained with metals that do not decrease.
- Ni is mostly contained in Zn.
- the crystal structures of Ni-Zn and Zn are greatly different. Also, the crystallized Zn does not become nuclei, so the solder structure does not become finer.
- solder paste in which a particle diameter is 5 to 300 nm, an ethanol solution containing nanoparticles containing one or more kinds of Ag, Au, and Cu, and a flux and solder powder are mixed, Since the solder composition after soldering is miniaturized, it is possible to improve the joint strength.
- Nanoparticles used in the present invention may be single metal Ag, Au, and Cu nanoparticles, and SiC, SiN, TiN, C, and Ni, which have been successfully formed into nanoparticles at present.
- Co, A1203, Sn02, Zr02, Ti02, Ce02, Ca02, Mn304, MgO, ITO (In203 + Sn02) and other components may be bonded to Ag, Au, and Cu. Even if Ag, Au, or Cu is added to nanoparticles of other components, the same effect is obtained because Ag, Au, Cu, and Zn on the surface of the fine powder react to produce Zn nuclei. can get.
- the nanoparticles used in the present invention may be one type of metal nanoparticle selected from Ag, Au, and Cu.
- nanoparticles that are a mixture of two or more types of Ag, Au, and Cu are used. Also good.
- the nanoparticle used in the present invention is a particle having a particle size on the order of nm, but it is difficult to produce a nanoparticle of less than 5 nm at present, and a particle exceeding lOOOnm.
- the core of the crystallized material is preferably 300 or less.
- the nuclei at the initial stage of Zn crystallization are considered to be even smaller than the added nanoparticle diameter.
- the present invention has a particle size of 5 to 300 nm, 0.01 mass% to 2.0 mass in the total amount of solder paste in which an ethanol solution containing nanoparticles containing one or more kinds of Ag, Au, and Cu and flux solder powder are mixed. % Preferred. If the amount of nanoparticles is less than 0.01 mass, the amount of nucleation of intermetallic compounds with Sn-Zn-based lead-free solder powder is small, and the effect of solder miniaturization cannot be obtained.
- nanoparticles When added in excess of 2.0% by mass, nanoparticles reacted with Sn-Zn lead-free solder significantly increase the liquidus temperature, lowering the fusion characteristics of the solder at low temperature, and Sn-Zn lead It cannot be used for parts that do not have the heat resistance characteristic of free solder alloys.
- nanoparticles are used to generate nuclei of Ag, Au, Cu and intermetallic compounds.
- Patent Document 2 when dissolved and added in Sn-Zn lead-free solder, The added Ag is completely melted, and the intermetallic compound and Zn nuclei in which Ag, Au, and Cu are dissolved are generated by probability theory, so that the crystallized product cannot be refined by such a method.
- the phenomenon in the present invention is that Zn nuclei are uniformly and uniformly dispersed in a liquid phase to such an extent that the flow characteristics of the liquid are not impaired.
- Yet another invention provides a solder paste obtained by mixing an ethanol solution containing one or more nanoparticles selected from Ag, Au, and Cu, a flux, and solder powder with a particle size of 5 to 300 nm. This is a method of miniaturizing the solder structure after soldering by using and soldering.
- Nanoparticles containing one or more types selected from Ag, Au, and Cu at 5 to 300 nm have a fine particle size and thus oxidize immediately upon contact with the outside air. Therefore, the nanoparticle is sealed in an inert gas or stored in oil so that it does not come into contact with the outside air. However, even if the nanoparticles are sealed in an inert gas, they will be exposed to the outside air during the manufacture of the solder paste, so that the reactivity with the Sn-Zn-based lead-free solder powder will be weakened. Teshima! /, Generate a lot of solder balls.
- solder paste is mixed with the stored oil together with solder powder and flux to produce solder paste, the oil itself has no solderability, so the solderability deteriorates and the solder ball is deteriorated. Will increase.
- pine resin or flux is not suitable for storage of nanoparticles because it reacts with nanoparticles.
- a powder having a particle size of 5 to 300 nm and containing at least one kind selected from Ag, Au, and Cu is dispersed in an alcohol solvent, and the powder and Mix with flux to produce solder paste.
- the alcohol solvent is a liquid that contains a hydroxyl group! Is.
- the hydroxyl group contained in the alcohol solvent promotes the action of dissociating into activator ions and removing the oxides when the flat active agent decomposes when heated by reflow.
- alcohol solvents used in the present invention include aliphatic alcohols such as methanol, ethanol, isopropanol, ethylene glycol, and diethylene glycol, aromatic alcohols such as talesol, terpene alcohols such as ⁇ -TVneol, Glycol ethers such as ethylene glycol monobutino enoate, diethylene glycol mono hexeno ethenore, diethylene mono 2-ethyleno hexeno ree enore, and pheneno les glycolenore are preferred.
- aliphatic alcohols such as methanol, ethanol, isopropanol, ethylene glycol, and diethylene glycol
- aromatic alcohols such as talesol
- terpene alcohols such as ⁇ -TVneol
- Glycol ethers such as ethylene glycol monobutino enoate, diethylene glycol mono hexeno ethenore, diethylene mono 2-ethyleno
- alcoholic solvents used in the present invention include terpene alcohols such as ⁇ -TVneol, which are difficult to absorb moisture, ethylene glycol mononomonobutylenoateol, diethyleneglycolenomonohexenoreethenole, diethylene mono2 —Glycol ethers such as ethylhexyl ether and phenol glycol are more preferred.
- the fluxes used in the examples and comparative examples of the present invention are as follows.
- the solder paste was produced by mixing a solder powder, a flux and a dispersion of nanoparticles into a stirrer.
- the solder paste formulation of the examples and comparative examples is as follows.
- Sn- 9Zn solder powder (20 ⁇ 40 ⁇ ⁇ ) 88. 5 mass 0/0 lOOnmAg 40% to diethylene glycol hexyl ether dispersion 0.025 wt% of the particles (as eight 8 weight, 0.01% by weight)
- Sn- 9Zn solder powder (20 to 40 mu m) 84. 5 mass 0/0 lOOnmAg 40% to diethylene glycol hexyl ether dispersion 5.0 mass% of the particles (as Ag amount, 2.0% by weight)
- Sn- 9Zn solder powder (20 ⁇ 40 ⁇ ⁇ ) 88. 5 mass 0/0 lOOnmAu 40% diethylene glycol hexyl ether particle dispersion 0.2 mass% (as Au amount, 0.08 wt%)
- Sn- 9Zn solder powder (20 to 40 mu m) 82. 5 mass 0/0 lOOnmAg 40% to diethylene glycol hexyl ether dispersion 7.5 mass% of the particles (as ⁇ amount, 3.0% by weight)
- Sn- 9Zn solder powder (20 ⁇ 40 ⁇ ⁇ ) 88. 5 mass 0/0 l, diethylene glycol hexyl ether 500nmAg particles 40% dispersion 0.2 wt% (as Ag amount, 0.08 wt%)
- test substrates of the examples and comparative examples after being allowed to cool for one day are observed with an electron microscope set at 1000 times to compare the miniaturization of solder structures.
- Table 1 shows the results of Examples and Comparative Examples.
- Figures 1 and 2 show typical structural changes after temperature cycling.
- Fig. 1 shows the structure refinement caused by the addition of the Ag nanoparticles of Example 2, which corresponds to ⁇ in the tissue refinement test.
- Fig. 2 shows the addition of Ag to the solder alloy from the beginning of Comparative Example 2, and the microstructure is reduced. It does not happen and falls under X in the microstructure refinement test.
- a solder paste is prepared by mixing nanoparticles, solder powder and flux according to the following storage method, and a solder ball test is performed to compare solder balls generated during heating.
- the flux used in this test was the same as that used in Example 1, and the composition of the solder paste was set so that each example and comparative example had a Cu content of 0.08% by mass.
- Ne-ol 40% dispersion 0.2 mass 0/0 (as Cu amount, 0.08 wt%)
- Comparative Example (1) (Powder stored in nitrogen is directly mixed with solder powder.)
- Heat medium oil 40% dispersion of 20nm Cu particles 0.2% by mass (as Cu amount, 0.08% by mass) Flux 11. 3% by mass
- Table 2 shows the results of Examples and Comparative Examples.
- solder paste of each example and comparative example is printed on an alumina substrate, and within 1 hour after printing, the alumina substrate is placed on a solder bath set at 250 ° C. to melt the solder paste.
- Example 1 the solidified solder paste solder of the example had a force that caused subdivision of the structure and the generation of cracks after the temperature cycle.
- the solidified solder paste of the comparative example solder paste had a temperature cycle. When cracked, cracks were observed.
- Comparative Example 3 with reference to Patent Document 3 the solder after reflow was in an unmelted state, and the Cu powder remained undissolved.
- Example 2 the solder paste in which the nanoparticles of the example were dispersed in an alcohol-based solvent was a force with little generation of solder balls. The thing generated many solder balls.
- FIG. 1 is a cross-sectional view of a solder structure of Example 2. Applicable to ⁇ in the microstructure refinement test.
- FIG. 2 is a cross-sectional view of the solder structure of Comparative Example 2. Applicable to X in the microstructure refinement test. Industrial applicability
- the solder paste according to the present invention having a particle size of 5 to 300 nm and containing a solution containing one or more kinds of nanoparticles selected from Ag, Au, and Cu, a flux and a solder powder is an Sn-Zn solder alloy. Even in the case of Sn-Ag solder alloys, Sn-Cu solder alloys, and Sn-A g-Cu solder alloys, it is possible to refine the solder structure by selecting nanoparticles that can be the core of each compound. Effect.
- Sn-Ag solder alloys, Sn-Cu solder alloys, and Sn-Ag-Cu alloys with a particle size of 5 to 300 nm and ethanol solutions and fluxes containing one or more types of nanoparticles that can be the core of each compound Solder paste in which solder powder is mixed has high bonding strength, and a solder alloy can be obtained.
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- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Electric Connection Of Electric Components To Printed Circuits (AREA)
- Powder Metallurgy (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP06756513.5A EP1889683B1 (en) | 2005-05-25 | 2006-05-24 | Lead-free solder paste |
JP2006527796A JP4493658B2 (ja) | 2005-05-25 | 2006-05-24 | 鉛フリーソルダペースト |
CN2006800231118A CN101208173B (zh) | 2005-05-25 | 2006-05-24 | 无铅焊膏及其制法 |
US11/920,962 US9185812B2 (en) | 2005-05-25 | 2006-05-24 | Lead-free solder paste |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2005-151805 | 2005-05-25 | ||
JP2005151805 | 2005-05-25 |
Publications (1)
Publication Number | Publication Date |
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WO2006126564A1 true WO2006126564A1 (ja) | 2006-11-30 |
Family
ID=37451988
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2006/310307 WO2006126564A1 (ja) | 2005-05-25 | 2006-05-24 | 鉛フリーソルダペースト |
Country Status (6)
Country | Link |
---|---|
US (1) | US9185812B2 (ja) |
EP (1) | EP1889683B1 (ja) |
JP (2) | JP4493658B2 (ja) |
KR (1) | KR101026970B1 (ja) |
CN (1) | CN101208173B (ja) |
WO (1) | WO2006126564A1 (ja) |
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US7686205B2 (en) * | 2006-07-19 | 2010-03-30 | Honda Motor Co., Ltd. | Method of joining members having different thermal expansion coefficients |
JP2013041683A (ja) * | 2011-08-11 | 2013-02-28 | Tamura Seisakusho Co Ltd | 導電性材料 |
JP2013107132A (ja) * | 2011-11-17 | 2013-06-06 | Samsung Electro-Mechanics Co Ltd | 鉛フリーはんだ合金及びその製造方法 |
CN104625466A (zh) * | 2015-01-21 | 2015-05-20 | 哈尔滨工业大学深圳研究生院 | 一种可以在低温下快速形成高温焊点的锡基焊料/铜颗粒复合焊料 |
JP2015188902A (ja) * | 2014-03-27 | 2015-11-02 | 日本電気株式会社 | はんだ組成物、はんだペースト、はんだ接合構造、及び電子機器 |
US9695521B2 (en) | 2010-07-19 | 2017-07-04 | Universiteit Leiden | Process to prepare metal nanoparticles or metal oxide nanoparticles |
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KR102394475B1 (ko) * | 2021-09-14 | 2022-05-04 | 마이크로컴퍼지트 주식회사 | 저융점 고신뢰성 솔더 입자, 이를 포함하는 수지 조성물 |
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JP4493658B2 (ja) | 2010-06-30 |
JP5754794B2 (ja) | 2015-07-29 |
EP1889683B1 (en) | 2016-02-03 |
EP1889683A1 (en) | 2008-02-20 |
KR101026970B1 (ko) | 2011-04-11 |
EP1889683A4 (en) | 2009-08-19 |
US9185812B2 (en) | 2015-11-10 |
US20090301606A1 (en) | 2009-12-10 |
KR20080015874A (ko) | 2008-02-20 |
CN101208173A (zh) | 2008-06-25 |
JPWO2006126564A1 (ja) | 2008-12-25 |
CN101208173B (zh) | 2010-05-19 |
JP2010120089A (ja) | 2010-06-03 |
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