Treatment of a simulated sludge by ultrasonic zero-valent iron/EDTA/Air process: Interferences of inorganic salts in polyaromatic hydrocarbon removal.

Waste Manag

Guangzhou Key Laboratory of Environmental Catalysis and Pollution Control, Guangdong Key Laboratory of Environmental Catalysis and Health Risk Control, School of Environmental Science and Engineering, Institute of Environmental Health and Pollution Control, Guangdong University of Technology, Guangzhou 510006, China.

Published: February 2019

Understanding the occurrence states of persistent organic pollutants such as polycyclic aromatic hydrocarbons (PAHs) in textile dyeing sludge is the key to their further treatment and disposal. Here, the effects of inorganic salts (silicate, sulfate, phosphate, hydroxide, and iron salts) that were typically rich in textile dyeing sludge on PAH adsorption by sludge and PAH degradation by an ultrasound (US) combined zero-valent iron/EDTA/Air (ZEA) system were studied in a simulated sludge system. The results showed that the simulated sludge containing inorganic salts had a larger specific surface area, which was beneficial for the adsorption of PAHs. More low-ring PAHs were adsorbed on the surface of the particles in the simulated sludge because of the inorganic salts, which was conducive to low-ring PAHs degradation by US/ZEA. The PAH removal rates were increased by 15.37% and 11.19%, respectively, in the presence of SiO and HPO. The yield of hydroxyl radicals (OH) was increased by 42.39% and 66.25% by SiO and HPO, respectively. The reason was that the oxidation of the ligand ([Fe(EDTA)]) formed by ethylenediaminetetraacetic acid (EDTA) and divalent iron was promoted by SiO and HPO. The formation of OH in the US/ZEA system was inhibited by the corrosion inhibition of SO on zero-valent iron (ZVI), the reaction of ferric salt with EDTA, and the reaction of Mg(OH) with the ligand ([Fe(EDTA)]). This work provides an essential theoretical insight into the role of the inorganic components of sludge in the removal of PAHs by advanced oxidation processes.

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http://dx.doi.org/10.1016/j.wasman.2019.01.009DOI Listing

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