Zhou, Qin, et al. (2024) Microwave assisted biomass derived carbon aerogel for highly efficient oxytetracycline hydrochloride degradation: Singlet oxygen mechanism and C vacancies accelerated electron transfer. Chemical Engineering Journal. https://doi.org/10.1016/j.cej.2024.150370

In the pursuit of sustainable solutions for environmental remediation, researchers have explored the microwave-assisted pyrolysis of plant biomass-derived α-cellulose and sodium lignosulfonate to develop biochar aerogel catalysts. These catalysts exhibit enhanced properties such as increased surface area, enriched functional groups, and abundant vacancies, paving the way for efficient peroxymonosulfate (PMS) activation and organic pollutant degradation under transition metal-free conditions.

The study reveals that microwave treatment and the inclusion of sodium lignosulfonate play pivotal roles in introducing thiophene S, enriching C=O groups, and enhancing C vacancies, thereby boosting the catalytic performance of the biochar aerogels. The optimal catalyst, C3S2, demonstrates exceptional capability in promoting PMS activation, leading to a remarkable 99.9% degradation of oxytetracycline hydrochloride (OTC) within just 15 minutes, with a high rate constant of 0.818 min^-1.

Furthermore, the investigation delves into the mechanism underlying OTC degradation, highlighting the involvement of key active sites such as C=O groups and thiophene S in the production of singlet oxygen (1O2) via PMS activation. Additionally, the enrichment of C vacancies facilitates electron transfer processes, further accelerating pollutant degradation.

The research not only sheds light on the design of metal-free biochar catalysts for efficient contaminant removal but also underscores the potential of biomass-derived materials in addressing environmental challenges. By elucidating the intricate pathways involved in pollutant degradation, this work contributes to advancing sustainable technologies for water treatment and ecosystem protection.



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