The morphologies and the elemental compositions of the developed biocomposites were analyzed by means of a Verios G4 UC scanning electron microscope (Thermo Scientific, Brno, Czech Republic) equipped with an energy dispersive X-ray spectroscopy analyzer (Octane Elect Super SDD detector, EDAX-AMETEK, Mahwah, NJ, USA) [67 (link)]. Before analysis, the samples were fractured in liquid nitrogen and dried, then fixed on aluminum stubs with double-adhesive carbon tape and coated with 10 nm gold using a Leica EM ACE200 Sputter coater (Leica Microsystem, Vienna, Austria) to provide material deterioration during electron beam exposure. SEM investigations were performed in high vacuum mode using a secondary electron detector (Everhart-Thornley detector, ETD) at an accelerating voltage of 10 kV.
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