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In the present study, thermal stability of α-Ga2O3 under vacuum and ambient pressure conditions was investigated in situ by x-ray diffraction and transmission electron microscopy (TEM). It was observed that the thermal stability of α-Ga2O3 increased by 200 °C when pressure was lowered from an atmospheric to a vacuum level. This finding can be explained by oxygen diffusion under different oxygen partial pressures. In addition, in situ TEM imaging revealed that, once past the decomposition temperature, the onset of phase change propagates from the top crystal surface and accumulates strain, eventually resulting in a fractural film. The mechanism of α-Ga2O3 to β-Ga2O3 transition is evaluated through experiments and is discussed in this manuscript.
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Comparative Study of Atmosphere Effect on Wood Torrefaction
Climate change, biomass utilization, and bioenergy recovery are among the biggest current global concerns. Wood is considered an environmentally benign material. Nevertheless, it must be processed for desired applications. Upon thermal treatment ranging from 180 °C to 280 °C, under low oxygen concentrations, wood becomes a material with improved dimensional stability, resistance to fungal attacks, grindability, hydrophobicity, and storage stability. Several strategies for wood treatment have been investigated over the course of the past decades, including the use of steam, nitrogen, smoke, vacuum, water, and hot oil. The goal of this work is to investigate the influence of pressure and atmosphere on the torrefaction of poplar. Through a systematic analysis of poplar wood samples treated under reduced pressures and different atmospheres, while keeping the same heating profile, it was possible to establish that changes observed for mass loss, color change, wood composition (via TGA/DTG analysis), functional groups (via FTIR), elemental analysis, and X-ray diffractograms relate directly to known reaction pathways occurring during torrefaction. Changes observed under reduced pressures have been associated with the relative concentration of oxygen in the reaction atmosphere and to the reduced diffusion times experienced by reactive by-products during the treatment. Conversely, extended diffusion times resulted in more significant changes for reactions carried out under N2, water vapor, and air.
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- Award ID(s):
- 1952402
- PAR ID:
- 10439461
- Date Published:
- Journal Name:
- Fibers
- Volume:
- 11
- Issue:
- 3
- ISSN:
- 2079-6439
- Page Range / eLocation ID:
- 27
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.3390/fib11030027
