Zango Zakariyya Uba, Khoo Kuan Shiong, Garba Abdurrahman, Kadir Haliru Aivada, Usman Fahad, Zango Muttaqa Uba, Da Oh Wen, Lim Jun Wei
Department of Chemistry, College of Natural and Applied Science, Al-Qalam University Katsina, 2137, Katsina, Nigeria; Institute of Semi-Arid Zone Studies, Al-Qalam University Katsina, 2137, Katsina, Nigeria.
Department of Chemical Engineering and Materials Science, Yuan Ze University, Taoyuan, Taiwan.
Environ Res. 2023 Mar 15;221:115326. doi: 10.1016/j.envres.2023.115326. Epub 2023 Jan 21.
Perfluorooctanoic acid (PFOA) has been identified as the most toxic specie of the family of perfluorinated carboxylic acids (PFCAs). It has been widely distributed and frequently detected in environmental wastewater. The compound's unique features such as inherent stability, rigidity, and resistance to harsh chemical and thermal conditions, due to its multiple and strong C-F bonds have resulted in its resistance to conventional wastewater remediations. Photolysis and bioremediation methods have been proven to be inefficient in their elimination, hence this article presents intensive literature studies and summarized findings reported on the application of advanced oxidation processes (AOPs) and photocatalytic degradation techniques as the best alternatives for the PFOA elimination from wastewater. Techniques of persulfate, photo-Fenton, electrochemical, photoelectrochemical and photocatalytic degradation have been explored and their mechanisms for the degradation and defluorination of the PFOA have been demonstrated. The major advantage of AOPs techniques has been centralized on the generation of active radicals such as sulfate (SO) hydroxyl (•OH). While for the photocatalytic process, photogenerated species (electron (e) and holes (h )) initiated the process. These active radicals and photogenerated species possessed potentiality to attack the PFOA molecule and caused the cleavage of the C-C and C-F bonds, resulting in its efficient degradation. Shorter-chain PFCAs have been identified as the major intermediates detected and the final stage entails its complete mineralization to carbon dioxide (CO) and fluoride ion (F). The prospects and challenges associated with the outlined techniques have been highlighted for better understanding of the subject matter for the PFOA elimination from real wastewaters.
全氟辛酸(PFOA)已被确认为全氟羧酸(PFCA)家族中毒性最强的物质。它已广泛分布于环境废水中,并经常被检测到。由于其多个强C-F键,该化合物具有诸如固有稳定性、刚性以及对苛刻化学和热条件的耐受性等独特特性,这导致其对传统废水处理具有抗性。光解和生物修复方法已被证明在消除该物质方面效率低下,因此本文进行了深入的文献研究,并总结了关于应用高级氧化工艺(AOPs)和光催化降解技术作为从废水中去除PFOA的最佳替代方法的研究结果。已探索了过硫酸盐、光芬顿、电化学、光电化学和光催化降解技术,并展示了它们对PFOA的降解和脱氟机制。AOPs技术的主要优势集中在产生诸如硫酸根(SO)、羟基(•OH)等活性自由基。而对于光催化过程,则是光生载流子(电子(e)和空穴(h ))引发该过程。这些活性自由基和光生载流子具有攻击PFOA分子并导致C-C和C-F键断裂的潜力,从而实现其有效降解。已确定短链PFCA是检测到的主要中间体,最终阶段是将其完全矿化为二氧化碳(CO)和氟离子(F)。已强调了与上述技术相关的前景和挑战,以便更好地理解从实际废水中去除PFOA这一主题。