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Hydrothermal liquefaction (HTL) is an effective way to treat solid wastes with high moisture content. The co-hydrothermal liquefaction (co-HTL) experiments of oily scum and poplar sawdust biochar at the different hydrothermal temperatures were performed in this work. The changes of the appearance and components of the liquid products were comprehensively studied. The results showed that the addition of biochar into oily scum significantly reduced the moisture content of the residue hydrochars obtained after co-HTL. As the hydrothermal temperature increased, the liquid products obtained from co-HTL turned clearer and lighter in color, and the recovery rate of the liquid products significantly increased. The co-HTL of bi-ochar and oily scum could effectively improve the liquid quality and enhance the recovery rate of hydrochars. The carbon numbers of the liquid products obtained from co-HTL were concentrated in C5-C11, which were main compositions of gas-oline. This work can provide basic data and theoretical reference for oily scum efficient treatment and engineering practice.

Hydrothermal liquefaction (HTL) is an effective way to treat solid wastes with high moisture content. The co-hydrothermal liquefaction (co-HTL) experiments of oily scum and poplar sawdust biochar at the different hydrothermal temperatures were performed in this work. The changes of the appearance and components of the liquid products were comprehensively studied. The results showed that the addition of biochar into oily scum significantly reduced the moisture content of the residue hydrochars obtained after co-HTL. As the hydrothermal temperature increased, the liquid products obtained from co-HTL turned clearer and lighter in color, and the recovery rate of the liquid products significantly increased. The co-HTL of bi-ochar and oily scum could effectively improve the liquid quality and enhance the recovery rate of hydrochars. The carbon numbers of the liquid products obtained from co-HTL were concentrated in C5-C11, which were main compositions of gas-oline. This work can provide basic data and theoretical reference for oily scum efficient treatment and engineering practice.

In the quest for more efficient solar thermal systems, accurately determining the thermal emittance of low-emissive materials is crucial in determining the power losses. This paper describes the calorimetric method designed to precisely measure the thermal emittance of Selective Solar Absorbers (SSAs) to be used in High Vacuum Flat Plate Collectors (HVFPCs). The method’s capability is demonstrated through the successful correction of thermal emittance values for copper samples of varying sizes, including dimensions down to 49 cm2. Results highlight the method’s potential to significantly reduce measurement errors associated with small-size and/or low-emittance samples, providing a path forward to improve the design and efficiency of SSAs. This research marks a significant step in advancing solar thermal technology by enabling emittance measurements with a precision better than 0.003, which is essential for the development of high-performance solar thermal absorbers. The method has also been applied to correct the thermal emittance value of SSA measured in previous measurement campaigns, and it allows a better estimation of the SSA efficiency conversion curve.

In the quest for more efficient solar thermal systems, accurately determining the thermal emittance of low-emissive materials is crucial in determining the power losses. This paper describes the calorimetric method designed to precisely measure the thermal emittance of Selective Solar Absorbers (SSAs) to be used in High Vacuum Flat Plate Collectors (HVFPCs). The method’s capability is demonstrated through the successful correction of thermal emittance values for copper samples of varying sizes, including dimensions down to 49 cm2. Results highlight the method’s potential to significantly reduce measurement errors associated with small-size and/or low-emittance samples, providing a path forward to improve the design and efficiency of SSAs. This research marks a significant step in advancing solar thermal technology by enabling emittance measurements with a precision better than 0.003, which is essential for the development of high-performance solar thermal absorbers. The method has also been applied to correct the thermal emittance value of SSA measured in previous measurement campaigns, and it allows a better estimation of the SSA efficiency conversion curve.

Degradation issues correlated to microstructural changes are the main obstacles to solid oxide fuel cell and electrolyser applications, making their identification and understanding fundamental steps. Coupling experimental activities with modelling, this work analyses the state-of-the-art Ni-YSZ (Yttria-Stabilized Zirconia)/YSZ/CGO (Cerium Gadolinium Oxide)/LSCF (Lanthanum Strontium Cobalt Ferrite)-CGO-based cell after 1000 h of galvanostatic electrolysis operation at fixed temperature and high steam composition in the inlet gas. Following a multiscale approach, the system behaviour is characterized through electrochemical impedance spectra and polarization curves as well as studying microstructure evolution, with a focus on Ni-cermet functional layer in view of Ni instability detected as the main degradation cause. A comparison with a cell consisting of the same initial geometrical structure and materials but aged in fuel cell mode allows to highlight the influence of operating mode and parameters on Ni-YSZ microstructure. Ni particle size and phase fraction variations experimentally observed on the electrode surface are correlated to water content and applied polarization simulated local values. Ni uneven distribution at the electrolyte interface and particle coarsening, above all, lead to an increase in polarization loss under electrolysis and fuel cell mode, respectively, since both penalise the charge transfer reaction and migration.

Degradation issues correlated to microstructural changes are the main obstacles to solid oxide fuel cell and electrolyser applications, making their identification and understanding fundamental steps. Coupling experimental activities with modelling, this work analyses the state-of-the-art Ni-YSZ (Yttria-Stabilized Zirconia)/YSZ/CGO (Cerium Gadolinium Oxide)/LSCF (Lanthanum Strontium Cobalt Ferrite)-CGO-based cell after 1000 h of galvanostatic electrolysis operation at fixed temperature and high steam composition in the inlet gas. Following a multiscale approach, the system behaviour is characterized through electrochemical impedance spectra and polarization curves as well as studying microstructure evolution, with a focus on Ni-cermet functional layer in view of Ni instability detected as the main degradation cause. A comparison with a cell consisting of the same initial geometrical structure and materials but aged in fuel cell mode allows to highlight the influence of operating mode and parameters on Ni-YSZ microstructure. Ni particle size and phase fraction variations experimentally observed on the electrode surface are correlated to water content and applied polarization simulated local values. Ni uneven distribution at the electrolyte interface and particle coarsening, above all, lead to an increase in polarization loss under electrolysis and fuel cell mode, respectively, since both penalise the charge transfer reaction and migration.

Dataset supporting publication of manuscript_GCB-B-RA-24-138

Dataset supporting publication of manuscript_GCB-B-RA-24-138