| Literature DB >> 33779142 |
Bin Zhao1, Maryam Borghei1, Tao Zou1, Ling Wang1, Leena-Sisko Johansson1, Johanna Majoinen1, Mika H Sipponen2, Monika Österberg1, Bruno D Mattos1, Orlando J Rojas1,3.
Abstract
Multiscale hemical">carbon supraparticles (<hemical">span class="Chemical">SPs) are synthesized by soft-templating lignin nano- and microbeads bound with cellulose nanofibrils (CNFs). The interparticle connectivity and nanoscale network in the SPs are studied after oxidative thermostabilization of the lignin/CNF constructs. The carbon SPs are formed by controlled sintering during carbonization and develop high mechanical strength (58 N·mm-3) and surface area (1152 m2·g-1). Given their features, the carbon SPs offer hierarchical access to adsorption sites that are well suited for CO2 capture (77 mg CO2·g-1), while presenting a relatively low pressure drop (∼33 kPa·m-1 calculated for a packed fixed-bed column). The introduced lignin-derived SPs address the limitations associated with mass transport (diffusion of adsorbates within channels) and kinetics of systems that are otherwise based on nanoparticles. Moreover, the carbon SPs do not require doping with heteroatoms (as tested for N) for effective CO2 uptake (at 1 bar CO2 and 40 °C) and are suitable for regeneration, following multiple adsorption/desorption cycles. Overall, we demonstrate porous SP carbon systems of low cost (precursor, fabrication, and processing) and superior activity (gas sorption and capture).Entities:
Keywords: CO2 capture; carbon supraparticles; cellulose nanofibrils; evaporation-induced self-assembly; lignin particles
Year: 2021 PMID: 33779142 DOI: 10.1021/acsnano.0c10307
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881