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It is shown that the LSF samples displayed a 3DOM architecture and were of a single-phase orthorhombic crystal structure.
It is shown that the Pr6O11 and Tb4O7 samples displayed a 3DOM architecture with polycrystalline wormhole-like mesoporous walls.
HRSEM images of M1 samples displayed a noticeable ordered pattern of hexagonal symmetry at the surface, see Fig. 1d.
Differential scanning calorimetry achieved on PHO/PLA50-blended samples displayed a lack of complete miscibility between both components.
It is shown that the x wt% Co3O4/3DOM LSCO samples displayed a 3DOM architecture and a high surface area of 29 32 m2/g.
The surface of the HPDL-treated samples exhibited a collection of grouped particles with pores and gaps, whereas the untreated samples displayed a continuous mono-structured plane surface.
It is shown that the xAu/3DOM LaCoO3 samples displayed a 3DOM architecture and a high surface area of 24 29 m2/g.
Dimethyl- and dibutyl phthalate components in the corresponding CER/phthalate samples displayed a strong carbonyl absorption band with maximum around 1728 cm−1.
However, Conserv samples displayed a reduction in strength between 56 and 91 days possibly due to the pore structure changes associated with increasing carbonation [48].
All samples displayed a straightforward behavior during stepwise demagnetization (Fig. 5a d), yielding reverse ChRM directions that show a directional similarity between samples treated by AFD and ThD.
From Fig. 5a c, we can see that all the PLGA/DOX samples displayed a uniform red fluorescence, indicating the homogeneous dispersion of DOX in the nanofibers.
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