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This evolution of primary size to secondary size was caused by the agglomeration of primary particles during drying process.
However, this method generates particles with a wide particle size distribution, which requires secondary size selection sometimes.
Therefore, extent of aggregation and secondary size of zinc ferrite NPs in water and cell culture medium was evaluated through dynamic light scattering (DLS).
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We thank Müller et al. for their interest in our article (Cho et al. 2009) and concur that the secondary sizing of particulate samples initially collected with a size-selective cascade impactor and then resuspended in solution is useful information.
Secondary particle size (hydrodynamic size) of zinc ferrite NPs in de-ionized water and cell culture medium was 312 and 289 nm, respectively.
From the distribution of measured values, we see that the secondary particle size is far greater than the primary particle size, as measured by SEM and TEM.
Although the surface area of the TiO2 catalyst is unaffected by the secondary particle size, the activity of the catalyst for TCE photo-oxidation exhibited strong dependency on the aggregate size.
We observed that the secondary particle size (hydrodynamic diameter) of zinc ferrite NPs was several times higher as compared with the primary size measured by TEM.
In the case where breakage occurs the model for secondary nuclei size distribution is proposed.
Spherical (Ni0.5Mn0.5)(OH 2 with different secondary particle size (3 μm, 10 μm in diameter) was synthesized by co-precipitation method.
The first constraint states that the capacity of the secondary network (size of spectrum) should be less than or equal the capacity of the primary network (PUs' network).
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