Tailoring Pore Architecture and Heteroatom Functionality of Polymeric Waste-Derived Nanoporous Carbon for CO2 Capture Applications

  • Akshata Pattanshetti
  • , Amruta Koli
  • , Vidhya Jadhav
  • , Xiao Ying Yu
  • , Radha Kishan Motkuri
  • , Sandip Sabale

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

This study proposes upcycling polymeric waste, i.e., waste floral foam, into high-performance nanoporous carbon that efficiently captures CO2. This paper presents strategies for improving the properties of nanoporous carbon, which aid in a superior CO2 capture performance. Initially, pristine nanoporous carbon was produced from waste floral foam using various KOH impregnation ratios. The nanoporous carbon with a 1:2 (waste floral foam:KOH) ratio exhibiting optimal CO2 capture capability was further advanced through single and dual atom doping. The doping of N and codoping of N,S atoms into the nanoporous carbon altered its textural and surface chemical properties, making them efficient for CO2 capture. Comparative CO2 capture studies of pristine nanoporous carbon (NC-x), N-doped nanoporous carbon (N-NC2), and N,S-codoped nanoporous carbon (N,S-NC2) demonstrate the superiority of N-doping. N-doped nanoporous carbon exhibited the largest ultramicroporosity (0.3100 cm3/g, 63.43%) and highest heteroatom content (34.94 atomic %), contributing to its enhanced CO2 capture capability (4.54 mmol/g). Implementing the “waste-to-depollution” approach, this research lays the groundwork for producing low-cost, environmentally friendly nanoporous carbon with remarkable CO2 capture attributes.

Original languageEnglish
Pages (from-to)17961-17971
Number of pages11
JournalIndustrial and Engineering Chemistry Research
Volume63
Issue number42
DOIs
StatePublished - Oct 23 2024

Funding

The authors are thankful to the Department of Science and Technology, New Delhi for DST-FIST (No/SR/FST/College-151/2013(C)) and the Department of Biotechnology, New-Delhi for DBT-Star College Scheme to Jaysingpur College, Jaysingpur. R.K.M. acknowledges the Laboratory Directed Research and Development (LDRD) program at the Pacific Northwest National Laboratory (PNNL). PNNL is operated by Battelle for the US Department of Energy (DOE) under Contract DE-AC05-76RL01830. X.Y.Y. was supported by the strategic Laboratory Directed Research and Development (LDRD) of the Physical Sciences Directorate of the Oak Ridge National Laboratory (ORNL). This manuscript has been authored by UT-Battelle, LLC under Contract No. DE-AC05-00OR22725 with the U.S. DOE. The United States Government retains and the publisher, by accepting the article for publication, acknowledges that the United States Government retains a nonexclusive, paid-up, irrevocable, worldwide license to publish or reproduce the published form of this manuscript, or allow others to do so, for United States Government purposes. The DOE will provide public access to these results of federally sponsored research in accordance with the DOE Public Access Plan (http://energy.gov/downloads/doe-public-access-plan).

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