首页> 外文期刊>Energy & fuels >Oxidative Desulfurization of Gas Oil Catalyzed by (TBA)(4)PW11Fe@PbO as an Efficient and Recoverable Heterogeneous Phase-Transfer Nanocatalyst
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Oxidative Desulfurization of Gas Oil Catalyzed by (TBA)(4)PW11Fe@PbO as an Efficient and Recoverable Heterogeneous Phase-Transfer Nanocatalyst

机译:(TBA)(4)PW11Fe @ PbO催化的瓦斯油氧化脱硫是一种高效且可回收的非均相相转移纳米催化剂

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摘要

In this paper, a tetra(n-butyl)ammonium salt of iron(III)-substituted phosphotungstate@lead oxide composite, (TBA)(4)P-W11Fe@PbO, was successfully synthesized by the thermal decomposition method as a nanocatalyst for oxidative desulfurization (ODS) of gas oil. The incorporation of the materials was confirmed by Fourier transform infrared spectroscopy (FTIR), ultraviolet visible (UV-vis), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and P-31 nuclear magnetic resonance (NMR) characterization methods. To evaluate the catalytic activity of (TBA)(4)PW11Fe@PbO, the ODS process was carried out using a CH3COOH/H2O2 oxidizing agent at 60 degrees C. From the attained results, the total sulfur and mercaptan content of real gas oil were reduced with 97% efficiency after 2 h. Furthermore, the various comparative experiments were performed to investigate the capability of (TBA)(4)PW11Fe@PbO in ODS of prepared model fuel. Results were indicated that the kinetics of sulfur oxidation fitted the pseudo-first-order kinetic model. The probable mechanism was proposed via the electrophilic mechanism through the formation of a peroxometalate intermediate complex with phase transfer properties. After 5 oxidation runs, the heterogeneous nanocatalyst was separated and recovered easily.
机译:本文通过热分解法成功地合成了铁(III)-取代的磷钨酸@氧化铅复合物(TBA)(4)P-W11Fe @ PbO的四(正丁基)铵盐作为纳米催化剂瓦斯油的氧化脱硫(ODS)。通过傅里叶变换红外光谱(FTIR),紫外可见(UV-vis),X射线衍射(XRD),扫描电子显微镜(SEM),能量色散X射线光谱(EDX)确认了材料的掺入,和P-31核磁共振(NMR)表征方法。为了评估(TBA)(4)PW11Fe @ PbO的催化活性,使用CH3COOH / H2O2氧化剂在60摄氏度下进行了ODS工艺。从所得结果中,得出了粗柴油的总硫和硫醇含量为2小时后效率降低97%。此外,进行了各种比较实验以研究(TBA)(4)PW11Fe @ PbO在制备的模型燃料的ODS中的能力。结果表明,硫的氧化动力学符合拟一级动力学模型。可能的机理是通过亲电机理通过形成具有相转移特性的过氧金属酸盐中间体配合物而提出的。进行5次氧化后,非均相纳米催化剂被分离并易于回收。

著录项

  • 来源
    《Energy & fuels》 |2017年第5期|5472-5481|共10页
  • 作者单位

    Univ Zanjan, Dept Chem, Fac Sci, POB 451561319, Zanjan, Iran;

    Univ Zanjan, Dept Chem, Fac Sci, POB 451561319, Zanjan, Iran;

    Univ Zanjan, Dept Chem, Fac Sci, POB 451561319, Zanjan, Iran;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 00:39:32

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