Wang Junli, Chen Kunpeng, Jin Bosen, Woo Wonsik, Lum Michael, Canchola Alexa, Zhu Yiwen, Men Yujie, Liu Jinyong, Lin Ying-Hsuan
Department of Environmental Sciences, University of California, Riverside, California 92521, United States.
Department of Chemical and Environmental Engineering, University of California, Riverside, California 92521, United States.
Environ Sci Technol. 2024 Dec 10;58(49):21850-21860. doi: 10.1021/acs.est.4c06805. Epub 2024 Nov 26.
Thermal treatment of perfluoroalkyl and polyfluoroalkyl substances (PFASs) presents a promising opportunity to halt the PFAS cycle. However, how co-occurring materials such as granular activated carbon (GAC) influence thermal decomposition products of PFASs, and underlying mechanisms remain unclear. We studied the pyrolysis of two potassium salts of perfluoroalkanesulfonates (PFSAs, CFSOK), perfluorobutanesulfonate (PFBS-K), and perfluorooctanesulfonate (PFOS-K), with or without GAC. PFBS-K is more stable than PFOS-K for pure standards, but when it is adsorbed onto GAC, its thermal stabilities and decomposition behaviors are similar. Temperatures and heating rates can significantly influence the decomposition mechanisms and products for pure standards, while these effects are less pronounced when PFSAs are adsorbed onto GAC. We further studied the underlying decomposition mechanisms. Pure standards of CFSOK can decompose directly in their condense phase by reactions: F(CF)SOK → F(CF)CF═CF + KFSO or F(CF)SOK → F(CF) + K + SO. GAC appears to facilitate breakage of the C-S bond to release SO at temperatures as low as 280 °C. GAC promotes fluorine mineralization through functional reactive sites. SiO is particularly important for the surface-mediated mineralization of PFASs into SiF. These findings offer valuable insights into optimizing thermal treatment strategies for PFAS-contaminated waste.
全氟烷基和多氟烷基物质(PFASs)的热处理为阻断PFAS循环提供了一个有前景的机会。然而,颗粒活性炭(GAC)等共存材料如何影响PFASs的热分解产物以及潜在机制仍不清楚。我们研究了两种全氟烷磺酸盐(PFSAs,CFSOK)的钾盐,全氟丁烷磺酸盐(PFBS-K)和全氟辛烷磺酸盐(PFOS-K)在有或没有GAC的情况下的热解。对于纯标准品,PFBS-K比PFOS-K更稳定,但当它吸附在GAC上时,其热稳定性和分解行为相似。温度和加热速率会显著影响纯标准品的分解机制和产物,而当PFSAs吸附在GAC上时,这些影响不太明显。我们进一步研究了潜在的分解机制。CFSOK的纯标准品可以通过以下反应在其凝聚相中直接分解:F(CF)SOK → F(CF)CF═CF + KFSO 或 F(CF)SOK → F(CF) + K + SO 。GAC似乎在低至280°C的温度下促进C-S键的断裂以释放SO 。GAC通过功能性反应位点促进氟矿化。SiO对于PFASs表面介导的矿化成SiF尤为重要。这些发现为优化PFAS污染废物的热处理策略提供了有价值的见解。