Abstract
Industrial waste salts, laden with toxic organic impurities, pose significant environmental hazards. Thermal treatment has emerged as a promising strategy to reduce these contaminants. However, previous studies have focused on total organic carbon removal. Still, this work utilizes advanced two-dimensional gas chromatography time-of-flight mass spectrometry (GC × GC-TOFMS) and pyrolysis gas chromatography-mass spectrometry (PY-GC/MS) to provide unprecedented detail on the release and transformation pathways of specific organic groups (aromatics, nitrogenous, halogenated, etc.) in pesticide waste salts. This study investigates waste salts under medium-temperature conditions (400–500°C) in inert and oxygen-containing atmospheres. Results indicate that under an oxygen-containing atmosphere, the removal rate surpassed 99% within 20 minutes at 400 and 500°C. Oxygen-containing conditions significantly improve the removal efficiency but leave more complex organic residue in the treated salt, which retains nitrogen-containing compounds, aliphatic hydrocarbons and oxygenates. Organic impurities follow distinct transformation pathways: volatile P-xylene produces styrene, ethylbenzene and benzaldehyde; nitrogen-containing compounds (e.g. amines) form complex nitrogen- and oxygen-containing products; and halogenated compounds cleave into shorter-chain halogenated derivatives. These findings offer crucial insights into the thermal behaviour of organic contaminants in waste salts and guide the further treatment process of waste salts.
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