Institute of Green Chemistry and Chemical Technology, School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, China.
Institute of Green Chemistry and Chemical Technology, School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, China.
J Colloid Interface Sci. 2021 Apr;587:202-213. doi: 10.1016/j.jcis.2020.09.069. Epub 2020 Sep 24.
Recently, the development of dual functional catalytic membrane for the synergistic degradation and filtration of persistent pollutants has attracted considerable attention in environmental remediation. Herein, novel CoFe alloy and CoFeO nanoparticles encapsulated in N-doped microtube composites (CoFe-NMTs) were firstly fabricated through in-situ pyrolysis of simple-source Prussian blue analogues (PBA). As expected, this unique structure not only inhibited the nanoparticles agglomeration, but also provided a "highway" that accelerated the Co/Co and Fe/Fe redox cycles. Therefore, CoFe-NMT-800 (0.1 g/L, pyrolyzed at 800 °C) achieved over 90% tetracycline (TC, 30 mg/L, 0.1821 min) removal after 30 min at a wide pH (2.55-9.55) by coupling with peroxymonosulfate (PMS, 0.3 g/L), which dramatically outperformed the majority of the reported catalysts (such as CoO, CoFe alloy, CoFeO and N-doped carbon nanotubes, etc.). Additionally, CoFe-NMTs-800 also exhibited excellent catalytic activity in the existence of inorganic anions (Cl, HCO and HPO) and natural organic matters (humic acid (HA)). Subsequently, CoFe-NMTs-800 was immobilized into polyvinylidene fluoride (PVDF) membrane as catalytic self-cleaning membrane via applying phase-inversion technology. It was found that CoFe-NMTs-800/PVDF membrane not only maintained high removal efficiency for TC degradation (over 90%) in TC/HA coexistence system, but also effectively eliminated the adverse effect of membrane fouling. Besides, the fabricated membrane also showed desirable reusability and neglectable metal leaching (0.003 mg/L Fe and 0.015 mg/L) with almost constant flux after five cycles. The quenching experiments and electron paramagnetic resonance (EPR) results clearly indicated that sulfate radicals (SO), hydroxyl radicals (OH and singlet oxygen (O) were responsible for TC degradation and SO was a major contributor. Significantly, this work was very meaningful to construct novel catalytic self-cleaning membrane for water purification.
最近,协同降解和过滤持久性污染物的双功能催化膜的发展在环境修复中引起了相当大的关注。在此,通过简单来源的普鲁士蓝类似物(PBA)的原位热解,首次制备了新型 CoFe 合金和 CoFeO 纳米粒子封装的 N 掺杂微管复合材料(CoFe-NMTs)。正如预期的那样,这种独特的结构不仅抑制了纳米粒子的聚集,而且还提供了一种“高速公路”,加速了 Co/Co 和 Fe/Fe 的氧化还原循环。因此,CoFe-NMT-800(0.1 g/L,在 800°C 下热解)在 30 分钟内通过与过一硫酸盐(PMS,0.3 g/L)耦合,在宽 pH 值(2.55-9.55)下实现了超过 90%的四环素(TC,30 mg/L,0.1821 min)的去除,这明显优于大多数报道的催化剂(如 CoO、CoFe 合金、CoFeO 和 N 掺杂碳纳米管等)。此外,CoFe-NMTs-800 在无机阴离子(Cl、HCO 和 HPO)和天然有机物(腐殖酸(HA))的存在下也表现出优异的催化活性。随后,通过相转化技术,将 CoFe-NMTs-800 固定到聚偏二氟乙烯(PVDF)膜上作为催化自清洁膜。结果发现,在 TC/HA共存体系中,CoFe-NMTs-800/PVDF 膜不仅保持了对 TC 降解的高去除效率(超过 90%),而且有效地消除了膜污染的不利影响。此外,所制备的膜在五个循环后通量几乎恒定,具有良好的可重复使用性和可忽略的金属浸出(0.003 mg/L 的 Fe 和 0.015 mg/L 的 Fe)。淬灭实验和电子顺磁共振(EPR)结果清楚地表明,硫酸盐自由基(SO)、羟基自由基(OH 和单线态氧(O)负责 TC 的降解,而 SO 是主要贡献者。值得注意的是,这项工作对于构建新型催化自清洁膜用于水净化具有重要意义。