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DOI 10.1016/j.chemosphere.2025.144309

Медицинская библиотека · Chemosphere · 2025

Boosting biodegradation and mineralization efficiencies of chlorinated VOCs: The synergy of H2O2 and biotrickling filtration.

Ghiasvand Shiva, Moussavi Gholamreza, Mohseni Madjid

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Аннотация

This study explores a new biodegradation process of H2O2-stimulated BTFs to remove perchloroethylene (PCE) from the contaminated air stream. BTF stimulated with H2O2 significantly boosted PCE biodegradation compared to conventional methods. Optimal parameters for H2O2-assisted PCE biodegradation were also identified (nominal inlet concentration = 150 ppm, EBCT = 30 s, H2O2/PCE molar ratio = 0.2). Under these optimum conditions, the BTF achieved a maximum PCE removal efficiency of around 95 %, a mineralization rate of 65 %, and an elimination capacity of 117 g/m3.h, demonstrating its effectiveness. The BTF maintained stable performance under various PCE loads, suggesting its applicability for industrial cases. Moreover, the study revealed a positive correlation between increasing H2O2/PCE ratios and the activities of key enzymes responsible for biodegradation including dehydrogenase)increased from 1.3 to 26.1 mg-TF/gbiomass), peroxidase (increased from 0 to 251 U/gbiomass), and catalase (increased from 0 to 7.8 U/gbiomass) when the ratio was increased from 0 to 0.2. The H2O2-stimulated BTF performed efficiently for biodegradation (>90 %) and mineralization (>60 %) of PCE at empty bed contact times between 20 and 60 s. Finally, the absence of PCE and toxic intermediates in the recycled liquid supports the efficient biodegradation of PCE in the developed system. In conclusion, H2O2-stimulated BTF shows promise as a sustainable and cost-effective approach for biodegradation of chlorinated organic compounds in contaminated air streams.

Для цитирования: Ghiasvand Shiva, Moussavi Gholamreza, Mohseni Madjid. Boosting biodegradation and mineralization efficiencies of chlorinated VOCs: The synergy of H2O2 and biotrickling filtration.. Chemosphere. 2025. DOI: 10.1016/j.chemosphere.2025.144309.

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