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Characterization of catalytic materials containing zeolites using n-hexane cracking reaction.

机译:使用正己烷裂化反应表征包含沸石的催化材料。

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摘要

ZSM-5 zeolites precursors were synthesized by hydrothermal crystallization method from aluminosilicate gels in the presence of organic templates:---tetrapropyl ammonium bromide, and diethanolamine at temperatures of 175°C under autogeneous pressure. The materials were characterized by powder X-ray diffraction, Infrared spectroscopy, and benzene adsorption. The course of crystallization was followed by examining the X-ray diffraction pattern of the calcined samples and the optical density ratio of the bands at 550cm-1 and 450cm -1 in the mid IR region of the structure spectra as a function of crystallization time. For a well crystalline material, the optical density ratio is 0.70; this ratio was found to be less if amorphous silica is present in zeolite.;The X-ray, IR and n-hexane cracking activity data suggests that these zeolite precursors are microcrystalline solid material in amorphous matrix with structures similar to that of ZSM-5. The infrared spectroscopy results were correlated with other structural data obtained by X-ray diffraction, adsorption measurements, and also with the results of catalytic test.;The catalytic activity of the samples has been evaluated for the n-hexane cracking in tubular fixed bed reactor at the temperature range of 300°C to 500°C. The Cracking Mechanism Ratio (CMR) calculated reveals that the n-hexane cracking reaction over the catalyst tested proceeds predominantly via protolytic route and catalytic activity of the TPABr-mediated samples increases with crystallinity. Apparent activation energies are remarkably similar in spite of differences in relative level of activity.
机译:在有机模板:-四丙基溴化铵和二乙醇胺的存在下,在自生压力下,通过铝硅酸盐凝胶通过水热结晶法合成ZSM-5沸石前体。通过粉末X射线衍射,红外光谱和苯吸附对材料进行表征。通过检查煅烧样品的X射线衍射图和在结构光谱的中IR区域中550cm-1和450cm -1处的谱带的光密度比随结晶时间的变化来跟踪结晶过程。对于良好结晶的材料,光密度比为0.70;对于高密度材料,为0.90。如果沸石中存在无定形二氧化硅,则发现该比率较小。; X射线,IR和正己烷裂解活性数据表明,这些沸石前体是无定形基质中的微晶固体材料,其结构与ZSM-5相似。红外光谱结果与通过X射线衍射,吸附测量获得的其他结构数据以及催化试验的结果相关联;;已经评估了样品在管状固定床反应器中对正己烷裂解的催化活性。在300°C至500°C的温度范围内。计算的裂化机理比率(CMR)表明,在被测催化剂上的正己烷裂化反应主要通过蛋白水解途径进行,TPABr介导的样品的催化活性随结晶度的增加而增加。尽管相对活性水平存在差异,但表观活化能仍非常相似。

著录项

  • 作者

    Umar, Yunusa.;

  • 作者单位

    King Fahd University of Petroleum and Minerals (Saudi Arabia).;

  • 授予单位 King Fahd University of Petroleum and Minerals (Saudi Arabia).;
  • 学科 Chemistry Physical.;Engineering Chemical.
  • 学位 M.S.
  • 年度 2001
  • 页码 133 p.
  • 总页数 133
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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