AI Article Synopsis

  • Nitrogen adsorption isotherms and the BET model are commonly used to estimate the surface area of biochar, but they often yield low surface area results that don't align with the material's high sorption capacities.
  • In contrast, this study suggests that water adsorption may provide a more accurate estimation of biochar surface area, as it showed better alignment with properties like cation exchange capacity.
  • Results indicated that while nitrogen gas adsorption energies were higher, the nitrogen surface areas were lower compared to those derived from water vapour, showing how pyrolysis temperature affects these measurements differently.

Article Abstract

Nitrogen adsorption isotherms, along with the BET model for interpretation, are recommended for estimating biochar surface area. The frequently measured small surface areas of biochars contrast with their high sorption and cation exchange capacities. We hypothesised that water adsorption provides a better tool for estimating the surface area of biochars. Although adsorption energy also appears to be a valuable surface characteristic, there is a lack of studies on this subject. We studied the surface areas and adsorption energies of three waste deposits - peat, willow dust and biochar prepared from these materials at different temperatures - using nitrogen and water vapour adsorption isotherms. The BET model accurately described all water vapour adsorption isotherms but failed for some nitrogen isotherms. Alternative methods for estimating surface areas and adsorption energies were proposed in cases where the BET model did not apply. Nitrogen adsorption was typically much lower than water vapour adsorption, and the estimated surface areas reflected this. However, nitrogen adsorption energies were significantly higher. Nitrogen surface areas increased with pyrolysis temperature, while water vapour surface areas decreased. The surface area estimated from nitrogen adsorption was generally much lower than needed to accommodate the surface-charged groups responsible for the cation exchange capacity of biochars.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11621813PMC
http://dx.doi.org/10.1038/s41598-024-81030-9DOI Listing

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