Abstract

The paper reports the synthesis of SiC nanowhiskers via a process that utilizes carbon and silica from the same renewable source without the addition of external Si precursors as a sustainable and cost-effective method. This study reports an improved and sustainable method of synthesizing silicon carbide (SiC) nanowhiskers using cornstalk cellulose char under microwave heating. The aim was to optimize the process and gain a deeper understanding of the formation and growth mechanism of SiC nanowhiskers from biomass under microwave treatment in a temperature range of 1200–1400 °C. The synthesized product was then characterized by various analytical techniques. The formation of SiC nanowhiskers (β-SiC) was promoted at higher reaction temperatures, increasing from 6.83 wt% at 1200 °C to 9.35 wt% at 1400 °C. The SiC nanowhiskers displayed straight rod and smooth cylindrical structures. The nanostructure of β-SiC was confirmed along the d-spacing (111) plane, with a characteristic lattice fringe spacing of 0.25 nm. The growth mechanism of the SiC nanowhiskers followed two reaction pathways of vapor-solid (VS) and the vapor-liquid-solid (VLS). Increased CO and CO2 concentrations due to the evolution of gaseous products (SiO and CO) from the reactive cellulose char led to the growth of SiC nanowhiskers under the solid-vapor mechanism. The presence of inherent metallic species, such as Fe in biochar was found to catalyze the formation and growth of SiC nanowhiskers.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.