In the present work, one near-eutectic and three hypoeutectic Sn-Ag-Cu alloys have been employed for soldering by induction heating. The alloys were produced by induction melting of high purity Ag, Cu, and Sn lumps. The melting behavior of the alloys was investigated by differential scanning calorimetry. The solder alloys were subsequently applied for soldering by conventional hot-plate heating as well as induction heating and both soldering times and peak temperatures were recorded during soldering. Solder joints of two copper sheets were produced. The electrical resistance, tensile strength, and microstructure were analyzed on each soldered joint. The results indicate that the physical and mechanical properties of solder joints are determined by their chemical composition and soldering technology. Induction soldered joints not only have a slightly higher electrical resistivity but also higher mechanical strength, except of the 0.3 wt.% Ag hypoeutectic solder. The highest increase in ultimate tensile strength (28%) was observed for induction soldered joints with 1 wt.% Ag hypoeutectic solder. This effect is ascribed to the homogenous distribution of the intermetallic compounds within the eutectic in the alloy microstructure. The homogenous distribution is aided by rotation of liquid solder due to eddy currents and high-frequency magnetic field generated during induction heating.
Small amounts of the rare-earth element Ce were added to the Sn-rich leadfree eutectic solders Sn-3.5Ag-0.7Cu, Sn-0.7Cu, and Sn-3.5Ag to improve their properties. The microstructures of the solders without Ce and with different amounts (0.1 wt.%, 0.2 wt.%, and 0.5 wt.%) of Ce were compared. The microstructure of the solders became finer with increasing Ce content. Deviation from this rule was observed for the Sn-Ag-Cu solder with 0.2 wt.% Ce, and for the Sn-0.7Cu eutectic alloy, which showed the finest microstructure without Ce. The melting temperatures of the solders were not affected. The morphology of intermetallic compounds (IMC) formed at the interface between the liquid solders and a Cu substrate at temperatures about 40°C above the melting point of the solder for dipping times from 2 s to 256 s was studied for the basic solder and for solder with 0.5 wt.% Ce addition. The morphology of the Cu 6 Sn 5 IMC layer developed at the interface between the solders and the substrate exhibited the typical scallop-type shape without significant difference between solders with and without Ce for the shortest dipping time. Addition of Ce decreased the thickness of the Cu 6 Sn 5 IMC layer only at the Cu/ Sn-Ag-Cu solder interface for the 2-s dipping. A different morphology of the IMC layer was observed for the 256-s dipping time: The layers were less continuous and exhibited a broken relief. Massive scallops were not observed. For longer dipping times, Cu 3 Sn IMC layers located near the Cu substrate were also observed.
The influence of increased Cu and Ag contents on the microstructure evolution in the utilized Sn-0.3Ag-0.7Cu (wt. %) solder was studied. The utilized solder was exploited in the wave soldering process at the temperatures of about 260 °C for several days. The samples investigation involved the differential scanning calorimetry, the scanning electron microscopy including the energy dispersive X-ray spectroscopy, and the X-ray diffraction techniques. To predict phase equilibria at various temperatures and temperature dependences of heat capacity, the Thermo-Calc software and the COST531 lead-free solder database were used. The original and the utilized solders were found to be very similar regarding the phase occurrence, but slightly differ from one another in microstructure evolution due to higher bulk contents of Cu in the latter solder. The obtained results contribute to both the better understanding of the microstructure evolution in low-silver Sn-Ag-Cu solders and the determination of compositional limits for those solders used in the wave soldering process.
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