非晶态中空CoSx增强丁基黄原酸钠的去除和抗菌活性及其可能的实际应用

Enhanced sodium butyl xanthate removal and antibacterial activity by amorphous hollow CoSx and its possible practical application

  • 摘要: 钴基金属有机框架材料因其卓越的催化和抗菌性能,在废水处理领域受到广泛关注。本研究通过溶剂热法硫化ZIF-67成功合成CoSₓ,其中CoS-0.25和CoS-1.00分别在去除丁基黄原酸钠(SBX)和抑制大肠杆菌(E.coli)方面表现出优异性能。CoS-0.25通过活化过一硫酸盐(PMS)在1分钟内去除89%的SBX,并在较宽pH范围(3-11)内保持高效去除性能。此外,CoS-0.25/PMS体系可以连续10小时保持80%以上的SBX去除率,在实际水体中去除率可达90%。同时,CoS-1.00表现出优于ZIF-67的抗菌性能,在120分钟内对E.coli的抗菌率达98%,最小抗菌浓度为31.30 μg/mL。这是因为CoS-0.25和CoS-1.00增强的亲水性促进了与SBX和细菌细胞的界面接触,也更有利于活性氧物种的产生。机制研究表明,超氧自由基(·O2)是SBX去除过程中的主要活性氧物种,S物种通过加速Co3+/Co2+氧化还原循环促进PMS活化。此外,活性氧物种通过破坏细菌细胞壁实现细菌灭活,从而获得强效抗菌性能。

     

    Abstract: Co-based metal-organic frameworks (MOFs) have gained significant attention in wastewater treatment owing to their exceptional catalytic and antibacterial properties. In this work, CoSₓ were successfullysynthesized via the sulfurization of ZIF-67 using a solvothermal method. Among the synthesized materials, CoS-0.25 and CoS-1.00 exhibited outstanding performance in the removal of sodium butyl xanthate (SBX) and the inhibition of Escherichia coli (E.coli), respectively. CoS-0.25 activated peroxymonosulfate (PMS) to remove 89% of SBX within 1 minute and maintained high removal efficiency over a broad pH range (3-11). Furthermore, the CoS-0.25/PMS system sustained an SBX removal rate of over 80% for 10 consecutive hours, achieving up to 90% removal in actual water bodies. Meanwhile, CoS-1.00 demonstrated antibacterial performance superior to that of ZIF-67, achieving a 98% antibacterial rate against E.coli within 120 minutes, with a minimum inhibitory concentration of 31.30 μg/mL. The enhanced hydrophilicity of CoS-0.25 and CoS-1.00 promoted interfacial contact with SBX and bacterial cells, respectively, and also facilitated the generation of reactive oxygen species (ROS). Mechanistic investigations revealed that the superoxide radical(·O2) was the primary ROS responsible for SBX removal, and S species accelerated the Co3+/Co2+redox cycle, thereby promoting PMS activation. In addition, ROS contributed to bacterial inactivation by disrupting the cell wall, resulting in potent antibacterial performance.

     

/

返回文章
返回