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Cells were smoothly seeded in the collagen-coated PLLA sponges by dropping a cell suspension solution onto the sponges.
The zeta-potential for CNA was over 30 mV that kept the nano-particle stable without aggregation when stored in suspension solution.
Using this bio-separator, antibody-coated magnetic beads have been successfully separated from the bio-buffer suspension solution and characterized in dynamic fluid flow.
An electromagnetic glassy carbon (GC) electrode was employed to collect the magnetite particles (0.25 10 mg dm−3) from the suspension solution.
Safranin, a kind of cationic organic dye, is introduced in this stage as a new-type dispersant to disperse GNS and CNT in water to form a suspension solution.
Such mixture was added to the suspension solution formed by dissolving HB in deionized water.
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Three suspension solutions were prefiltered through a 0.45 μm pore mill filter.
The tubes were taken out at different intervals of time and the suspension solutions were centrifuged.
The suspension solutions were put into 50-mL Teflon-lined hydrothermal synthesis autoclave reactors and maintained at 260 °C for 24 h, then cooled down naturally to room temperature.
Prior to irradiation, the suspension solutions of the catalysts were kept in dark for about 15 min to attain the adsorption desorption equilibrium between RhB dye and catalytic surface systems.
Three suspension solutions containing 250, 500, and 1000 ppm of SiO2 nanostructures were prepared in the presence of 0.1% (V/V) Triton X-100 at 25 °C as recommend in pesticide formulations [33].
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