生物固体热处理期间全氟和多氟烷基物质破坏后氟的命运:热力学研究

Energies Pub Date : 2024-07-15 DOI:10.3390/en17143476
Savankumar Patel, P. Halder, I. Hakeem, Ekaterina Selezneva, Manoj Kumar Jena, G. Veluswamy, Nimesha Rathnayake, Abhishek Sharma, A. Sivaram, Aravind Surapaneni, Ravi Naidu, M. Megharaj, Arun K. Vuppaladadiyam, Kalpit Shah
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摘要

全氟烷基和多氟烷基物质(PFAS)是一组氟化合成化学物质,具有很强的难降解性、毒性和生物累积性,已在世界各地的生物固体中检测到,对人类和环境构成潜在风险。最新研究表明,在热处理过程中,PFAS 中的有机 C-F 键会被破坏,并有可能矿化成无机氟化物。本研究的重点是生物固体热处理过程中的热力学平衡研究和全氟辛烷磺酸破坏后氟化合物的归宿。结果表明,气相氟化合物主要是氟化氢(HF)和碱氟化物,而固相氟化合物包括碱土氟化物及其尖晶石。挥发物中水分和氧气含量较高,增加了气相中氟化氢的浓度。然而,添加矿物质可显著减少气相中 HF 的排放,并增强固相中作为 CaF2 尖晶石的氟捕获。本研究还调查了原料成分对氟的命运的影响。原料中的高灰分和低挥发性物质减少了氟化氢气体的排放,增加了固态产品中的氟捕集。这项工作的发现有助于设计具有优化操作条件的热处理系统,从而在热处理含全氟辛烷磺酸的生物固体时最大限度地减少含氟物质的释放。
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The Fate of Fluorine Post Per- and Polyfluoroalkyl Substances Destruction during the Thermal Treatment of Biosolids: A Thermodynamic Study
Per- and polyfluoroalkyl substances (PFAS) are a group of fluorinated synthetic chemicals that are highly recalcitrant, toxic, and bio-accumulative and have been detected in biosolids worldwide, posing potential risks to humans and the environment. Recent studies suggest that the organic C-F bond in PFAS can be destructed and potentially mineralised into inorganic fluorides during thermal treatment. This study focuses on thermodynamic equilibrium investigations and the fate of fluorine compounds post-PFAS destruction during biosolid thermal treatment. The results indicate that gas-phase fluorine compounds are mainly hydrogen fluoride (HF) and alkali fluorides, whereas solid-phase fluorine compounds include alkaline earth fluorides and their spinels. High moisture and oxygen content in the volatiles increased the concentration of HF in the gas phase. However, adding minerals reduced the emission of HF in the gas phase significantly and enhanced the capture of fluorine as CaF2 spinel in the solid phase. This study also investigates the effect of feedstock composition on the fate of fluorine. High ash content and low volatile matter in the feedstock reduced HF gas emissions and increased fluorine capture in the solid product. The findings of this work are useful in designing thermal systems with optimised operating conditions for minimising the release of fluorinated species during the thermal treatment of PFAS-containing biosolids.
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