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首页> 外文期刊>Catalysis in industry >Development of Technology for the Production of Microspherical Alumina Support for the Alkane Dehydrogenation Catalyst: III. The Effect of the Phase Composition of Microspherical Supports on Their Thermal Stability
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Development of Technology for the Production of Microspherical Alumina Support for the Alkane Dehydrogenation Catalyst: III. The Effect of the Phase Composition of Microspherical Supports on Their Thermal Stability

机译:用于烷烃脱氢催化剂的微球形氧化铝载体生产技术的发展:III。微球形载体的相组成对其热稳定性的影响

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This publication continues a series of our reports on the optimization of preparation conditions for obtaining a thermally stable support for the alkane dehydrogenation catalyst. The phase composition effect on the stability, particle size distribution, structure, texture, and mechanical properties of supports heated to 1100°C is reported. Microspherical alumina supports obtained by successive thermal and hydrothermal treatments of gibb-site are compared to commercial supports obtained by the thermochemical activation (TCA) of gibbsite. The dimensions of the support granules decrease upon heating because of shrinkage, which is governed by the phase composition of the granules and by the packing of their constituent boehmite and alumina crystallites. Three tem- perature intervals can be distinguished in the shrinkage of the granules. In region I (<600°C), there is intensive shrinkage via the diffusion glide of crystallites, the mechanical strength of the granules remaining invariable. In region II (600–900°C), the polymorphic transformations of alumina accompanied by sintering via surface diffu- sion do not affect the dimensions and strength of the granules. In region III (>900–1000°C), shrinkage takes place via coalescent sintering. For commercial manufacturing of microspherical alkane dehydrogenation catalysts and for ensuring their stability at 550–900°C, it is recommended to use alumina supports containing the minimum possible amount of χ-Al_2O_3. As the single-phase boehmite support obtained by our technology is heated to 1100°C, its granules shrink by no more than 14.4% and show an attrition resistance of 89% or above. The support based on the gibbsite TCA products, which contains 14–23 wt % χ-Al_2O_3, is characterized by 3–5% greater gran- ule shrinkage and 6–12% lower mechanical strength.
机译:该出版物继续了我们关于优化制备条件的一系列报告,以获得用于烷烃脱氢催化剂的热稳定载体。据报道相组成对加热到1100℃的载体的稳定性,粒度分布,结构,织构和机械性能的影响。通过对三水铝石现场连续热处理和水热处理获得的微球形氧化铝载体与通过三水铝石的热化学活化(TCA)获得的商业载体进行了比较。由于收缩,载体颗粒的尺寸在加热时减小,收缩由颗粒的相组成以及它们的勃姆石和氧化铝微晶的堆积控制。颗粒的收缩可以区分三个温度间隔。在区域I(<600°C)中,由于微晶的扩散滑动而产生了强烈的收缩,而颗粒的机械强度保持不变。在II区(600-900°C),氧化铝的多晶型转变以及通过表面扩散进行烧结不会影响颗粒的尺寸和强度。在区域III(> 900–1000°C),收缩是通过聚结烧结发生的。为了商业化生产微球形烷烃脱氢催化剂并确保其在550–900°C的稳定性,建议使用含有尽可能少的χ-Al_2O_3的氧化铝载体。当通过我们的技术获得的单相勃姆石载体被加热到1100°C时,其颗粒收缩不超过14.4%,并且显示出89%或更高的耐磨耗性。基于菱铁矿三氯乙酸产品的支撑物,其含量为14–23 wt%的χ-Al_2O_3,其特征是颗粒收缩率提高了3–5%,机械强度降低了6–12%。

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