Heterogeneous catalysts for electro-Fenton degradation of cytostatic drug cytarabine

CAMCIOĞLU Ş., ÖZYURT B., Oturan N., Portehault D., Trellu C., Oturan M. A.

Chemosphere, cilt.370, 2025 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 370
  • Basım Tarihi: 2025
  • Doi Numarası: 10.1016/j.chemosphere.2024.143892
  • Dergi Adı: Chemosphere
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, PASCAL, Aerospace Database, Aqualine, Aquatic Science & Fisheries Abstracts (ASFA), Artic & Antarctic Regions, BIOSIS, Biotechnology Research Abstracts, CAB Abstracts, Chemical Abstracts Core, Chimica, Communication Abstracts, Compendex, EMBASE, Environment Index, Food Science & Technology Abstracts, Geobase, Greenfile, Metadex, Pollution Abstracts, Public Affairs Index, Veterinary Science Database, Civil Engineering Abstracts
  • Anahtar Kelimeler: Carbon nanotubes, Cytostatic, Heterogeneous electro-Fenton, Magnetic nanocomposite, Reduced graphene oxide, Wastewater treatment
  • Ankara Üniversitesi Adresli: Evet

Özet

In the present work, a reduced graphene oxide (rGO) modified-Fe3O4 doped bifunctional carbon felt cathode (rGO-Fe3O4/CF) that is capable of generating and converting H2O2 into hydroxyl radicals (•OH) on-site was fabricated, thus removing the need for an external catalyst. In addition, an rGO-modified cathode (rGO/CF) with high H2O2 production efficiency and a heterogeneous Fenton catalyst (CNT-Fe3O4) with magnetic properties were fabricated. The study examined the degradation and mineralization of the cytostatic drug cytarabine (CYT) using two HEF configurations: (i) a bifunctional cathode rGO-Fe3O4/CF and (ii) a combination of the rGO/CF cathode with CNT-Fe3O4 catalyst. The effects of parameters such as catalyst concentration, initial pH, and applied current were studied. HPLC and ion chromatography analyses were used to identify carboxylic acids and inorganic end-products, respectively. The results show that 0.1 mM CYT was completely degraded within 18 min at an applied current of 300 mA in the HEF system with the rGO-Fe3O4/CF bifunctional cathode. Total organic carbon (TOC) analysis revealed that the bifunctional cathode system achieved 98.2% mineralization of CYT after 4 h of treatment at 300 mA. Using the rGO/CF cathode and CNT-Fe3O4 catalyst cell, total degradation of 0.1 mM CYT occurred within 7 min, and nearly total mineralization (97.3% TOC removal) was achieved at 300 mA after 4 h.