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Optimization of chemically activated carbon derived from malt bagasse for CO₂ adsorption: a simplex-centroid approach

Giovanna C. Carlos; Lucas H. S. Crespo; Pedro H. C. Voloch; Aline A. R. Andrade; Pedro H. V. Ribeiro; Faissal Robbin; Vitor C. Almeida; Lucas Spessato
Environmental Science and Pollution Research · Vol. 33, Issue 9 · pp. 3962-3981 · 2026

Abstract

The intensification of the greenhouse effect has been primarily driven by anthropogenic CO₂ emissions, leading to significant climate change. Among the strategies to mitigate CO₂ emissions from industrial activities, adsorption using activated carbons (ACs) derived from renewable sources stands out as a promising approach. Activated carbons were prepared via chemical activation of malt bagasse, a brewing industry by-product, using NaOH, Na₂C₂O₄, Na₂CO₃, and their mixtures as activating agents. The augmented simplex-centroid method was employed to optimize the process and obtain an activated carbon (ACₒₚ) with high BET surface area. The materials were characterized by proximate analysis, N₂ physisorption, thermogravimetric analysis (TGA), scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), and Raman spectroscopy. CO₂ adsorption experiments were performed at different temperatures to assess performance. The optimized carbon (ACₒₚ) exhibited a well-developed porous structure and high surface area, achieving a CO₂ adsorption capacity of 2.83 mmol g⁻ 1 at 273 K. The results demonstrated that NaOH-activated carbon provides favorable properties for CO₂ capture, confirming the feasibility of malt bagasse as a sustainable precursor for efficient adsorbent materials.

Bibliographic Information

JournalEnvironmental Science and Pollution Research
PublisherSpringer
Publication Date2026-02-27
Publication Year2026
Volume33
Issue9
Pages3962-3981
Document TypeJournal Article
eISSN1614-7499
DOI10.1007/s11356-026-37557-7

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NARA Access Coverage1994-01-01~Current
Journal Homepagehttps://www.springer.com/journal/11356
Publisher PageOpen Publisher Page
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