Impact of pyrolysis heating methods on biochars with enhanced CO2/N2 separation and their incorporation in 3D-printed composites

resumo

N-doped biochars, derived from chitosan sourced from waste crustaceous shells, were produced via microwave- assisted pyrolysis at temperatures ranging from 400 to 800 degrees C to enhance CO2 2 and N2 2 separation. Their performance was compared with biochars from conventional pyrolysis. Microwave-derived biochars exhibited superior CO2 2 adsorption capacity at 25 degrees C and 100 kPa (0.78 - 1.56 mmol g- 1 ) compared to conventionally produced ones (0.55 - 1.43 mmol g-- 1 ). Increasing the pyrolysis temperature up to 600 degrees C significantly improved biochar properties, including surface area, pore volume, and CO2 2 adsorption capacity. Microwave-derived biochar featured enhanced surface area, larger pore volumes, and unique morphologies, requiring, on average, 61 % less preparation time. The higher ultramicroporosity and N-species concentration correlated with superior performance in the biochar produced at 600 degrees C. In gas mixture experiments (20 % CO2 2 and 80 % N2) 2 ) under flow conditions, these biochars showed rapid adsorption/desorption rates due to enhanced macroporosity at samples produced at 600 and 800 degrees C, facilitating gas diffusion along the ultramicropores. Adsorption heat analysis indicated that the CO2 2 adsorption is predominantly driven by physisorption, supported by complete sample regeneration when applying N2 2 flux or increasing the temperature during desorption. The study also explores the feasibility of 3D-printing a composite using the most effective biochar and inorganic polymers sourced from waste, presenting potential benefits for industrial applications.

palavras-chave

PORE-SIZE CHARACTERIZATION; CARBON-DIOXIDE CAPTURE; MICROPOROUS ADSORBENTS; MICROWAVE PYROLYSIS; SLOW PYROLYSIS; ADSORPTION; ISOTHERMS; BIOMASS; PHASE

categoria

Engineering

autores

Correia, I; Ilkaeva, M; Castellino, M; Bocchini, S; Novais, RM; Mafra, L; Gonçalves, NPF; Lourenço, MAO

nossos autores

agradecimentos

This work was developed within the scope of the project CICECO-Aveiro Institute of Materials, UIDB/50011/2020 (DOI 10.54499/UIDB/50011/2020) , UIDP/50011/2020 (DOI 10.54499/UIDP/50011/2020) & LA/P/0006/2020 (DOI 10.54499/LA/P/0006/2020) , financed by national funds through the FCT/MCTES (PIDDAC) . This work has received funding from the European Research Council (ERC) under the European Union's Horizon 2020 Research and Innovation Program (Grant Agreement 865974) . FCT is also acknowledged by M.I. and M.A. O.L. for Researcher positions (CEECIND/00546/2018 and CEECIND/01158/2021 (DOI: 10.54499/2021.01158.CEECIND/CP1659/CT0022) , respectively) . M.I. also acknowledges the Spanish Ministry of Science, Innovation and Universities for the "Beatriz Galindo" Scholarship (MU-23-BG22/00145) . N.G. and M.A.O.L acknowledge the funding from the European Union's Horizon Europe research and innovation program under the Marie Sklodowska-Curie Actions PF grant agreement No 101065059 and ERA-PF grant agreement No 101090287. R.N. would like to thank FCT project MAXIMUM (PTDC-CTM-CTM-2205-2020, DOI 10.54499/PTDC/CTM-CTM/2205/2020) .

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