Issue 36, 2021

Flexible nanoporous activated carbon for adsorption of organics from industrial effluents

Abstract

This paper reports a study involving the formation of a self-assembled polymeric monolayer on the surface of a high surface area activated carbon to engineer its affinity towards organic contaminants. A nanoporous activated carbon cloth with a surface area of ∼1220 m2 g−1 and a pore volume of ∼0.42 cm3 g−1 was produced by chemical impregnation, carbonisation and high-temperature CO2 activation of a commercially available viscose rayon cloth. The subsequent modification with a silane polymer resulted in a nanoscale self-assembled monolayer that made it selective towards organic solvents (contact angle <10°) and repellant towards water (contact angle >145°). The adsorbent showed more than 95% efficiency in the separation of various types of oil/water mixtures under neutral, basic and acidic conditions. Benefiting from inherent nanoscale features, a robust hierarchical structure and a thermally stable monolayer (∼300 °C), this nanoporous adsorbent maintained high efficiency for more than 20 cycles and separated surfactant stabilised emulsion with >92% oil removal efficiency. The adsorbent was studied extensively with a series of advanced characterisation techniques to establish the formation mechanism and performance in emulsion separation. Findings from this work provide crucial insights towards large-scale implementation of surface engineered activated carbon-based materials for a wide range of industrial separation applications.

Graphical abstract: Flexible nanoporous activated carbon for adsorption of organics from industrial effluents

Supplementary files

Article information

Article type
Paper
Submitted
20 May 2021
Accepted
26 Aug 2021
First published
27 Aug 2021

Nanoscale, 2021,13, 15311-15323

Flexible nanoporous activated carbon for adsorption of organics from industrial effluents

U. Zulfiqar, N. Kostoglou, A. G. Thomas, C. Rebholz, A. Matthews and D. J. Lewis, Nanoscale, 2021, 13, 15311 DOI: 10.1039/D1NR03242A

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