Emulsification processes are very sensitive to the time scale during which the dispersed phase is introduced into the continuous phase. A series of experiments were conducted across a transitional phase inversion path, which often leads to formation of nanoemulsions, with the speed of incorporation of the second phase (water) into the first phase (oil) being altered. The optimum condition could only be achieved if the optimum composition was maintained for a critical time. A slow addition (addition time > 60 s) of water to the oil allows the transitional phase inversion to become operative, leading to formation of sub-micrometer droplets. A very fast addition of the water phase (<5.0 s) caused the catastrophic phase inversion mechanism to become dominant, leading to formation of rather large drops. In the intermediate range of addition time, 20−40 s, both inversion mechanisms have contributed to drop formation, at least locally, and as a result skewed or bimodal drop size distributions were formed. The results indicate that while spontaneous emulsification is fast, it is not instantaneous. At a low surfactant concentration, the droplet size was only slightly affected by the rate of addition.
The interplay between porosity and electromigration can be used to manipulate atoms resulting in mass fabrication of nanoscale structures. Electromigration usually results in the accumulation of atoms accompanied by protrusions at the anode and atomic depletion causing voids at the cathode. Here we show that in porous media the pattern of atomic deposition and depletion is altered such that atomic accumulation occurs over the whole surface and not just at the anode. The effect is explained by the interaction between atomic drift due to electric current and local temperature gradients resulting from intense Joule heating at constrictions between grains. Utilizing this effect, a porous silver substrate is used to mass produce free-standing silver nanorods with very high aspect ratios of more than 200 using current densities of the order of 108 A/m2. This simple method results in reproducible formation of shaped nanorods, with independent control over their density and length. Consequently, complex patterns of high quality single crystal nanorods can be formed in-situ with significant advantages over competing methods of nanorod formation for plasmonics, energy storage and sensing applications.
Reduction in the sintering temperature of metal powders by lowering particle size into the nanoparticle range has resulted in a new class of porous sintered joining materials.Especially promising are sintered silver based materials which can be used to form bonds between wide-bandgap semiconductor die and circuit boards for use in high temperature applications. This work shows that for these materials the exterior sintered silver surface oxidizes preventing surface morphology changes, while the interior pore surfaces of the porous silver remain largely oxide-free. These pore surfaces facilitate fast atomic movement resulting in grain growth and changes in the internal microstructure.Morphology changes in the temperature range 200-400 °C are presented both as statistical averages of grain size and, uniquely in this type of study, by tracking individual pores and grains. It is shown that the internal structure will undergo changes during high temperature storage in contrast to the stable outer surface. A new technique, utilizing the electromigration effect to check the relative surface mobility of atoms in the interior pores and exterior surfaces was used to support the conclusions deduced from thermal ageing 2 experiments. Finally, we speculate that the stability of the exterior surface could be reproduced in the interior if the chemistry of the paste was altered to allow formation of a passivating layer on the interior pores during the final stages of the sintering process, resulting in formation of a stable die attach material for applications of up to 400 °C, for which there is an urgent need.
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