Advancement in Fenton-like reactions using PVA coated calcium peroxide/FeS system: Pivotal role of sulfide ion in regenerating the Fe(II) ions and improving trichloroethylene degradation

Abstract

This study demonstrated the prolonged benefits of polyvinyl-coated calcium peroxide (PVA@CP) in Fe(II)/nFeS mediated Fenton-like reaction. PVA@CP was prepared by a coating of PVA on calcium peroxide (CP) and synthesized nano-sized iron sulfide (nFeS) was characterized by scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HR-TEM) with energy dispersive spectroscopy (EDS) elemental mapping, X-ray diffractometry (XRD), X-ray photoelectron spectroscopy (XPS), inductively coupled plasma optical emission spectroscopy (ICP-OES) and Fourier transmission infrared (FTIR) techniques. Trichloroethylene (TCE) degradation in various oxic environments (H2O2, CP, or PVA@CP) was investigated using Fe(II)/nFeS, and the slowest rate constant of 0.031 M−1 min−1 with 91 % TCE removal highlighted the long-lasting effects of PVA@CP. The effect of initial solution pH revealed that the acidic condition was most favorable. PVA@CP system accumulated the least amount (6.34 mg/L) of Fe(III) than H2O2 and CP systems. Electron paramagnetic resonance (EPR) and scavenging tests highlighted that free hydroxyl radicals (HOfree) contributed dominantly in H2O2 system while both free and surface-bound species participated well in CP and PVA@CP systems. Moreover, the insight mechanism of regenerated Fe(II) on the nFeS surface was explored by XPS. Both oxidation and reduction of sulfur were discussed and declared that S(-II) was responsible for regenerating Fe(II). The recycling sample checked the reusability of nFeS, and 98.8 % TCE removal in actual groundwater emphasized that PVA@CP/Fe(II)/nFeS is a viable technique. In conclusion, the PVA@CP/Fe(II)/nFeS system is highly recommended for long-lasting remediation of TCE contaminated groundwater.