Abstract

An Fe0-participated O3/H2O2 (Fe0-O3/H2O2) process was applied to remove refractory organic matter (OM) in semi-aerobic aged refuse biofilter (SAARB) leachate arising from treating mature landfill leachate. The degradation and transformation characteristics of refractory OM were revealed at molecular level. Removal efficiencies of aromatic substances were 63.55% by the Fe0-O3/H2O2 process (much higher than in other single or binary processes), and fulvic- and humic-like substances were more effectively degraded by this process than by other treatments. According to Fourier transform-ion cyclotron resonance mass spectrometry (FT-ICR MS), 6645 categories of OM in SAARB leachate were identified. Although there was little difference in number of OM categories after treatment using the single-O3 and Fe0-O3/H2O2 processes, Fe0-O3/H2O2 process can better reduce OM relative abundance. It is noteworthy that the Fe0-O3/H2O2 process more effectively degraded CHONS compounds than the single-O3 process, while also producing more CHO compounds having higher bio-availability. The enhanced degradation efficiency of the Fe0-O3/H2O2 process were attributed to the formation of the Fenton process initiated by leached Fe2+ and H2O2. The heterogeneous catalytic effect from iron (hydro) oxides for O3/H2O2 also increased the treatment capacity of the Fe0-O3/H2O2 process, resulting in better total organic carbon removal. The Fe0-O3/H2O2 process is an efficient method for removing refractory OM in SAARB leachate.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.