Ultrasonic Spray Nozzle-Mediated Green Activation for Hierarchical Pore-Structured Carbon Beads

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • Michael Hough
  • Artur Deditius
  • Neil Robinson
  • Gerd Elmar Schröder-Turk
  • Kirkensgaard, Jacob Judas Kain
  • Volodymyr M. Gun’ko
  • Alexander V. Neimark
  • Katsumi Kaneko
  • Piotr Kowalczyk

This study focuses on enhancing sustainability through energy-efficient methods in producing hierarchically structured porous carbons. A novel approach, utilizing an ultrasonic spray nozzle-quartz tube reactor (USN-QTR), is introduced for fabricating carbon beads with customizable ultra-, super-, and mesopores. This study showcases noteworthy results from subjecting spherical char particles to activation processes involving carbon dioxide, a mixture of carbon dioxide and micron-sized water droplets, and highly concentrated supercritical steam at a temperature of 1173 K for durations of 3 and 5 h. Through pulse-field gradient nuclear magnetic resonance measurements, it was noted that carbon beads produced using USN-generated highly concentrated supercritical steam displayed remarkably elevated intrabead self-diffusivity of n-hexane. Inductively coupled plasma-optical emission spectroscopy demonstrates superior gold recovery kinetics from cyanide solutions compared to that from an industrial benchmark. The energy expenditure for USN-generated steam, producing carbon beads with an apparent surface area of 2691 m2/g, is estimated at 97 J per 1 m2 of carbon. This contrasts with the traditional steam generation method requiring approximately the energy of 190 J/m2 for activated carbon with an SBET of 2130 m2/g, making the USN-assisted activation method a more environmentally friendly and sustainable option with nearly half the energy consumption.

OriginalsprogEngelsk
TidsskriftACS Sustainable Chemistry and Engineering
Vol/bind12
Udgave nummer2
Sider (fra-til)737-750
Antal sider14
ISSN2168-0485
DOI
StatusUdgivet - 2024

Bibliografisk note

Funding Information:
We would like to acknowledge the support from the Australian Microscopy and Microanalysis research facility at the Centre for Microscopy, Characterisation, and Analysis, University of Western Australia. We would like to thank M. Kowalczyk for assistance with ICP-OES measurements. We acknowledge Nicholas Corrente and Shivam Parashar, Rutgers University, for their help with PSD calculations. A.V.N. acknowledges support from the CBET NSF grant No 1834339. N.R. acknowledges support from the Forrest Research Foundation and thanks Prof Mike Johns (University of Western Australia) for access to the NMR equipment.

Publisher Copyright:
© 2023 American Chemical Society.

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