Department of Civil & Environmental Engineering, Auburn University, Auburn, AL 36849, USA.
School of Environment and Energy, Peking University Shenzhen Graduate School, Shenzhen 518055, China.
Water Res. 2022 Jul 15;220:118650. doi: 10.1016/j.watres.2022.118650. Epub 2022 May 23.
GenX, the ammonium salt of hexafluoropropylene oxide dimer acid, has been used as a replacement for perfluorooctanoic acid. Due to its widespread uses, GenX has been detected in waters around the world amid growing concerns about its persistence and adverse health effects. As relevant regulations are rapidly evolving, new technologies are needed to cost-effectively remove and degrade GenX. In this study, we developed an adsorptive photocatalyst by depositing a small amount (3 wt.%) of bismuth (Bi) onto activated-carbon supported titanate nanotubes, Bi/TNTs@AC, and tested the material for adsorption and subsequent solid-phase photodegradation of GenX. Bi/TNTs@AC at 1 g/L was able to adsorb GenX (100 µg/L, pH 7.0) within 1 h, and then degrade 70.0% and mineralize 42.7% of pre-sorbed GenX under UV (254 nm) in 4 h. The efficient degradation also regenerated the material, allowing for repeated uses without chemical regeneration. Material characterizations revealed that the active components of Bi/TNTs@AC included activated carbon, anatase, and Bi nanoparticles with a metallic Bi core and an amorphous BiO shell. Electron paramagnetic resonance spin-trapping, UV-vis diffuse reflectance spectrometry, and photoluminescence analyses indicated the superior photoactivity of Bi/TNTs@AC was attributed to enhanced light harvesting and generation of charge carriers due to the UV-induced surface plasmon resonance effect, which was enabled by the metallic Bi nanoparticles. OH radicals and photogenerated holes (h) were responsible for degradation of GenX. Based on the analysis of degradation byproducts and density functional theory calculations, photocatalytic degradation of GenX started with cleavage of the carboxyl group and/or ether group by OH, h, and/or e, and the resulting intermediates were transformed into shorter-chain fluorochemicals following the stepwise defluorination mechanism. Bi/TNTs@AC holds the potential for more cost-effective degradation of GenX and other per- and polyfluorinated alkyl substances.
GenX,全氟辛烷磺酸氧化物二聚体酸的铵盐,已被用作全氟辛酸的替代品。由于其广泛的用途,GenX 已在世界各地的水域中被检测到,同时人们对其持久性和不良健康影响的担忧也与日俱增。由于相关法规正在迅速发展,因此需要新的技术来经济有效地去除和降解 GenX。在这项研究中,我们通过在负载在钛酸盐纳米管上的活性炭(TNTs@AC)上沉积少量(3wt.%)的铋(Bi)来制备一种吸附光催化剂,即 Bi/TNTs@AC,并对该材料吸附和随后对 GenX 的固相光降解进行了测试。在 1g/L 的 Bi/TNTs@AC 可以在 1 小时内吸附 GenX(100μg/L,pH7.0),然后在 4 小时内,在 UV(254nm)照射下,降解 70.0%并矿化 42.7%预吸附的 GenX。高效降解还使材料再生,无需化学再生即可重复使用。材料特性表明,Bi/TNTs@AC 的活性成分包括活性炭、锐钛矿和 Bi 纳米颗粒,其中 Bi 纳米颗粒具有金属 Bi 核和无定形 BiO 壳。电子顺磁共振自旋捕获、紫外-可见漫反射光谱和光致发光分析表明,Bi/TNTs@AC 的优越光活性归因于光诱导表面等离子体共振效应增强了光捕获和载流子的产生,这是由金属 Bi 纳米颗粒实现的。OH 自由基和光生空穴(h)负责 GenX 的降解。根据降解副产物的分析和密度泛函理论计算,GenX 的光催化降解首先通过 OH、h 和/或 e 断裂羧基和/或醚键开始,随后,生成的中间体通过逐步脱氟机制转化为短链含氟化学品。Bi/TNTs@AC 具有更经济有效地降解 GenX 和其他全氟和多氟烷基物质的潜力。