Improving dispersion stability of nanofluids through ultrasonication has been shown to be effective. Determining specific conditions of ultrasonication for a certain nanofluid is necessary. For this purpose, nanofluids of varying nanoparticle concentrations were prepared and studied to find out a suitable and rather mono-dispersed concentration (i.e., 0.5 vol.%, determined through transmission electron microscopy (TEM) analyses). This study aims to report applicable ultrasonication conditions for the dispersion of Al2O3 nanoparticles within H2O through the two-step production method. The prepared samples were ultrasonicated via an ultrasonic horn for 1-5h at two different amplitudes (25% and 50%). The microstructure, particle size distribution (PSD), and zeta potentials were analyzed to investigate the dispersion characteristics. Better particle dispersion, smaller aggregate sizes, and higher zeta potentials were observed at 3 and 5h of ultrasonication duration for the 50% and 25% of sonicator power amplitudes, respectively.
Nanofluids are promising in many fields, including engineering and medicine. Stability deterioration may be a critical constraint for potential applications of nanofluids. Proper ultrasonication can improve the stability, and possibility of the safe use of nanofluids in different applications. In this study, stability properties of TiO2-H2O nanofluid for varying ultrasonication durations were tested. The nanofluids were prepared through two-step method; and electron microscopies, with particle size distribution and zeta potential analyses were conducted for the evaluation of their stability. Results showed the positive impact of ultrasonication on nanofluid dispersion properties up to some extent. Ultrasonication longer than 150min resulted in re-agglomeration of nanoparticles. Therefore, ultrasonication for 150min was the optimum period yielding highest stability. A regression analysis was also done in order to relate the average cluster size and ultrasonication time to zeta potential. It can be concluded that performing analytical imaging and colloidal property evaluation during and after the sample preparation leads to reliable insights.