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DOI 10.1007/s11356-026-37557-7

Медицинская библиотека · Environmental science and pollution research international · 2026

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

Carlos Giovanna C, Crespo Lucas H S, Voloch Pedro H C, Andrade Aline A R, Ribeiro Pedro H V, Robbin Faissal, Almeida Vitor C, Spessato Lucas

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Аннотация

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.

Для цитирования: Carlos Giovanna C, Crespo Lucas H S, Voloch Pedro H C, Andrade Aline A R, Ribeiro Pedro H V, Robbin Faissal, Almeida Vitor C, Spessato Lucas. Optimization of chemically activated carbon derived from malt bagasse for CO₂ adsorption: a simplex-centroid approach.. Environmental science and pollution research international. 2026. DOI: 10.1007/s11356-026-37557-7.

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