首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Activate hydrogen peroxide for efficient tetracycline degradation via a facile assembled carbon-based composite: Synergism of powdered activated carbon and ferroferric oxide nanocatalyst
【24h】

Activate hydrogen peroxide for efficient tetracycline degradation via a facile assembled carbon-based composite: Synergism of powdered activated carbon and ferroferric oxide nanocatalyst

机译:激活过氧化氢,以通过容易组装的碳基复合材料进行有效的四环素降解:粉末状活性炭和铁氧化物纳米催化剂的协同作用

获取原文
获取原文并翻译 | 示例
           

摘要

Magnetic carbon@ferroferric oxide nanocatalyst (C@FONC), a composite material comprising powdered activated carbon (PAC) and ferroferric oxide nanocatalyst (FONC), was prepared using chemical co-precipitation. In this study, we evaluated the performance and complete pathway of tetracycline (TC) degradation in a C@FONC/H2O2 system. Moreover, the toxicity of TC and its intermediates was estimated. TC degradation in the C@FONC/H2O2 system followed pseudo-first-order kinetics, and the TC removal efficiency reached 97% in 120 min (TC0 = 150 ppm). The electron spin resonance (ESR) analysis and free radical quenching experiments indicated the generation of center dot OH and HO2 center dot during the reaction. The investigation of the reaction mechanisms revealed the complementary performances between C@FONC adsorption and heterogeneous Fenton-like reaction in the TC degradation process. The stability of C@FONC recycling was also measured by multiple cycles of reactions, and the TC removal rate still reached 85.8% after nine cycles. In addition, the superparamagnetism and negligible iron leaching of the C@FONC/H2O2 system represented significant improvements relative to PAC and the conventional homogeneous Fenton process, making it a promising composite for applications in advanced oxidation processes.
机译:使用化学共沉淀,制备磁性碳氧化物纳米催化剂(C @ FONC),包括粉末活性炭(PAC)和铁氧化物纳米催化剂(FONC)的复合材料。在这项研究中,我们评估了C @ FONC / H2O2系统中四环素(TC)降解的性能和完整途径。此外,估计了Tc及其中间体的毒性。 C @ FONC / H2O2系统中的TC劣化跟踪伪第一阶动力学,TC去除效率在120分钟内(TC0 = 150ppm)达到97%。电子自旋共振(ESR)分析和自由基淬火实验表明,在反应过程中,在中央点OH和HO2中心点产生。反应机制的研究揭示了在TC降解过程中的C @ FONC吸附和异质芬顿的反应之间的互补性能。 C 2 FONC再循环的稳定性也通过多循环的反应来测量,并且在九个循环后,TC去除率仍达到85.8%。此外,C @ FONC / H2O2系统的超分度和可忽略的铁浸出具有相对于PAC和常规均匀Fenton工艺的显着改善,使其成为高级氧化过程中应用的有望的复合材料。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号