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首页> 外文期刊>Materials Research Bulletin >Highly efficient deep desulfurization of fuels by meso/macroporous H_3PW_(12)O_(40)/TiO_2 at room temperature
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Highly efficient deep desulfurization of fuels by meso/macroporous H_3PW_(12)O_(40)/TiO_2 at room temperature

机译:中/大体积H_3PW_(12)O_(40)/ TiO_2在室温下对燃料进行高效的深度脱硫

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摘要

This paper described the synthesis of meso/macroporous phosphotungstic acid (HPW) /TiO2 catalyst with quatemary ammonium bromide and monodispersed polystyrene spheres (PS) as dual-template. The synthetic parameters, such as concentration of the templates and the alky chain length of quaternary ammonium bromide was studied carefully and optimized to generate catalyst with regulated porous features. The chemical properties of the catalyst was also investigated, X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) measurements confirmed the Keggin-type HPW were highly dispersed on the TiO2 framework. The optimal meso/macroporous HPW/TiO2 catalyst exhibited excellent catalytic activity in the oxidation of refractory sulphur compounds such as benzothiophene (BT), dibenzothiophene (DBT), and 4,6-dimethyldibenzothiophene (4,6-DMDBT). DBT was removed within 2 h at 30 degrees C under selected reaction conditions and the apparent activation energy for DBT oxidation was calculated to be 45.7 kJ/mol. The high ODS reaction rate of catalyst could be attributed to the combination of unique meso/macroporous architecture allowing for efficient mass transport of reactants and products in pore channel and its high surface area, large mesoporous size, and pore volume enabling sufficient exposure of catalytic active sites. Moreover, the meso/macroporous HPW/TiO2 catalyst also exhibited excellent reusability with no obviously degradation even after eight cycles.
机译:本文以季铵溴化铵和单分散聚苯乙烯球(PS)为双模板,描述了介孔/大分子磷钨酸(HPW)/ TiO2催化剂的合成。仔细研究了合成参数,例如模板的浓度和季铵溴化物的烷基链长,并对其进行了优化,以制备具有可调节多孔特性的催化剂。还研究了催化剂的化学性质,X射线衍射(XRD)和傅里叶变换红外(FT-IR)测量证实Keggin型HPW高度分散在TiO2骨架上。最佳的介孔/大分子HPW / TiO2催化剂在难处理的含硫化合物(如苯并噻吩(BT),二苯并噻吩(DBT)和4,6-二甲基二苯并噻吩(4,6-DMDBT))的氧化中表现出出色的催化活性。在选定的反应条件下,于30摄氏度于2小时内除去DBT,计算得出DBT氧化的表观活化能为45.7 kJ / mol。催化剂的高ODS反应速率可归因​​于独特的介孔/大分子结构的结合,允许在孔道中有效地传输反应物和产物,并且其表面积大,介孔尺寸大和孔体积大,从而可以充分暴露催化活性物质网站。而且,中/大体积HPW / TiO 2催化剂也显示出优异的可重复使用性,即使经过八次循环也没有明显的降解。

著录项

  • 来源
    《Materials Research Bulletin》 |2018年第9期|210-219|共10页
  • 作者单位

    Wuhan Univ Technol, Sch Mat Sci & Engn, Wuhan 430070, Hubei, Peoples R China;

    Wuhan Univ Technol, Dept Chem, Wuhan 430070, Hubei, Peoples R China;

    Wuhan Univ Technol, Sch Mat Sci & Engn, Wuhan 430070, Hubei, Peoples R China;

    Wuhan Univ Technol, Dept Chem, Wuhan 430070, Hubei, Peoples R China;

    Wuhan Univ Technol, Dept Chem, Wuhan 430070, Hubei, Peoples R China;

    Wuhan Univ Technol, Dept Chem, Wuhan 430070, Hubei, Peoples R China;

  • 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

    Meso/macroporous structure; Phosphotungstic acid; Oxidative desulfurization; Room temperature;

    机译:中/大结构;磷钨酸;氧化脱硫;室温;

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