The sol–gel method was used to prepare rattan-based silicon carbide (R–SiC) composite ceramics under different pyrolysis parameters through adjustment of the temperature and retention time of the one-step pyrolysis process. The crystalline phases, microscopic morphology, element distribution and specific surface area of the silicon carbide (SiC) were characterized by X-ray diffraction (XRD), Fourier transform-infrared spectroscopy (FT-IR), X-ray fluorescence spectrometer (XRF), field-emission scanning electron microscope (FESEM), transmission electron microscopy (TEM), energy dispersive X-ray analysis (EDX), and N2 physisorption. The results showed that the R–SiC prepared at different pyrolysis parameters was able to retain the porous structure of pristine rattan stem. The R–SiC prepared at 1500 ℃ for 120 min possessed the lowest density (0.25 g/cm3), the largest specific surface area (43.38 m2/g) and the highest SiC yield (44.24%). The SiC whisker was the major SiC morphology on the cross section of the R–SiC. Furthermore, the pyrolysis parameters were optimized with the SiC preparation process reaction mechanism, and material transformation methods were also discussed. This one-step pyrolysis process simplified the preparation of biogenic SiC ceramics and thus provided a potential route for the value-added utilization of rattan.
Rattan-based silicon carbide (R-SiC) ceramics, R-SiC SiO2 and R-SiC Si , were successfully prepared from silica (SiO 2 ) sol and silicon (Si) powder, respectively. The rattan powder was impregnated, respectively, with SiO 2 sol at ambient temperature and liquid melt-Si at high temperature. This was followed by one-step direct pyrolysis at 1500°C under an argon (Ar) atmosphere. The final SiC samples were analyzed using mass analysis, X-ray diffraction (XRD), X-ray fluorescence (XRF), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscope (SEM), energy dispersive X-ray analysis (EDAX), and nitrogen (N 2 ) physisorption techniques. Experimental results showed that the mass residual of R-SiC Si (42.56 wt%) was almost equal to R-SiC SiO2 (42.45 wt%). However, R-SiC SiO2 had a higher yield of SiC, a higher specific surface area and a more intact porous morphology preserved from the rattan biomass. In addition, some rod-like SiC whiskers and tablet-like SiC particles were found in R-SiC SiO2 . By comparison, R-SiC Si had a large amount of unreacted Si, as well as certain amount of SiC and unreacted C. Thus, it can be concluded that SiO 2 sols are more appropriate for use in preparation of SiC from rattan, whatever the porous microstructure, yield, and purity of SiC.
The efficient conversion of biomass into biofuels is closely associated with the topochemistry of the cell wall. In this study, the topochemical correlation between carbohydrates and lignin in the Eucommia ulmoides cell wall was investigated in situ by confocal Raman microscopy. The carbohydrates and lignin were mainly collocated in the secondary wall of the fiber, ray parenchyma, and vessel in E. ulmoides. High carbohydrates were associated with low lignin or vice versa, indicating that a high concentration of carbohydrates leads to a drop in the degree of lignification. Furthermore, the band intensity ratio of S-and G-lignin to carbohydrates (I1333/I2889 and I1274/I2889) in morphologically distinct regions of fiber was calculated. In accordance with the wet chemical analysis, a higher ratio of lignin to carbohydrates was observed within the middle layer of the 3-year-old E. ulmoides fiber secondary wall. The results potentially extend the current understanding of the carbohydrate and lignin topochemistry in woody biomass and may facilitate an efficient wood bioconversion process in future biorefineries.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.