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Flyash augmented FeO as a heterogeneous catalyst for degradation of stabilized landfill leachate in Fenton process. | LitMetric

Flyash augmented FeO as a heterogeneous catalyst for degradation of stabilized landfill leachate in Fenton process.

Chemosphere

Department of Civil Engineering, National Institute of Technology, Tiruchirappalli, Thuvakudi, Tamil Nadu, 620 015, India. Electronic address:

Published: March 2020

In this study magnetite (FeO) was augmented over coal flyash and analyzed for the effectiveness as a catalyst in heterogeneous Fenton process for the degradation of persistent organic pollutant present in stabilized landfill leachate. FeO and flyash augmented FeO was prepared by simple chemical precipitation method and both had magnetic nature. XRD, FTIR and SEM with EDX characterization were consummated for both catalysts. The Fenton experiments were performed in batch mode and to identify the optimal operating condition for effective COD removal the leachate pH, catalysts and HO dosages were varied. The reusability of the catalysts was studied. To understand the degradation mechanism adsorption study, Fenton oxidation of benzoic acid and scavenging experiments with KI and NaF were performed. It was witnessed that flyash augmented FeO exhibited 84.7% of COD degradation which was 12.3% of higher removal efficiency than FeO at optimum pH 3, 0.05 M HO and 1000 mg/L of catalyst dosage in 100 min reaction time. This flyash augmented FeO showed 68% of TOC removal and good increment in biodegradability. Poor NH-N removal was observed in the Fenton treatment process. Decrease in aromaticity was found based on SUVA value and also indicated the removal of organic matter. Similarly, reusability and stability were higher than FeO. The results indicate that flyash augmented FeO is a competent catalyst in heterogeneous Fenton process for treatment of mature leachate. The usage of waste material flyash with FeO decreases the co-aggregation of FeO and improves the catalytic performance.

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http://dx.doi.org/10.1016/j.chemosphere.2019.125189DOI Listing

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