Laboratory tests reveal enhanced degradation of BPA using a sludge-based catalyst activated by peroxymonosulfate, suggesting potential for resource recovery.
The increasing production of residual sludge has heightened interest in its resource utilization. In this study, municipal sewage sludge was pretreated with HCl-HF-HCl mixed acid etching and then pyrolyzed to prepare a sludge-based catalyst (MSF). The effects of acid etching on the physicochemical properties of the catalyst and its ability to activate peroxymonosulfate (PMS) for degrading bisphenol A (BPA) were systematically investigated. Results showed that acid etching removed inorganic impurities, optimized the pore structure, and increased the specific surface area to 248.06 m2/g. It also exposed more carbon defects and active sites, while enhancing surface oxygen-containing functional groups and graphitic nitrogen. The MSF/PMS system achieved nearly 100% BPA degradation within 90 min, far exceeding the control sample (MS). Quenching experiments and electron paramagnetic resonance (EPR) analyses confirmed that singlet oxygen (1O2) played a dominant role, accompanied by an electron transfer-mediated nonradical pathway. Electrochemical tests further demonstrated the enhanced electron conduction capability of MSF, which facilitated PMS activation. Moreover, MSF exhibited high adaptability and stability over a broad pH range (3–11) and in real water matrices, demonstrating great potential for practical applications. This study provides a theoretical foundation and technical support for sludge resource recovery and the development of efficient catalysts.
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An et al. (2026) studied this question.
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