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The washed particles were analysed by scanning electron microscopy, characterized by an elemental analyser and analysed for the presence of pesticides and mycotoxins.
The main chemical element distributions of the particles were analysed using energy-dispersive X-ray (EDX) spectroscopy.
These structural elements: the coarse porosities, the metallic binding phase and the embedded "abradable" particles were analysed by quantitative metallography.
These crystallised mannitol particles were analysed in terms of micromeritic properties, morphology, DSC, FT-IR, and in vitro fine particle fraction (FPF) and emitted dose (ED) of SS.
PM2.5 particles were analysed for a total of 31 elements by inductively coupled plasma mass spectrometer in order to identify the sources.
The particles were analysed with Transmission electron microscopy (TEM).
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A limitation of cryoelectron microscopy (cryo-EM) is that it requires the particles being analysed to be identical or nearly identical.
Oxidative pyrolysis of pine wood particles was analysed thermo-gravimetrically.
To exclude the possibility of generalized transduction, the frequency of packaging of the genes mecA, tetK and blaZ (encoding resistance to methicillin, tetracycline, and penicillin, respectively) into phage particles was analysed by relative quantification (Supplementary Table S5).
Rotations of the particles are analysed using physical experiments, an analytical model and a DEM numerical simulation.
The residence time distribution of solid particles is analysed by DEM and compared with experimental results in a pilot plant excluding combustion.
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