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In Situ Observation of Mesophase Formation and Coaiescence in Catalytic Hydroconversion of Vacuum Residue Using a Stirred Hot-Stage Reactor

机译:用搅拌热阶段反应器在真空残留催化水耦合中的中间相形成和共同化的原位观察

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A microreactor equipped with a view window and a stirrer was used to observe mesophase formation in Athabasca vacuum residue with and without catalyst The effect of stirring on mesophase formation and its growth and coalescence was studied during the cracking of vacuum residue under hydrogen at 4.8 MPa and 440 °C. Stirring can result in a bimodal distribution of size of mesophase domains. The forced coalescence of mesophase droplets by the stirrer led to the formation of very large mesophase regions (bulk mesophase), which coexisted with a large number of small micrometer-sized mesophase domains. The addition of catalyst likely had both chemical and physical effects on the formation and growth of mesophase. The catalyst gave a delay in the onset of mesophase formation as a chemical effect and a decrease in the amount of bulk mesophase regions by suppressing the coalescence of smaller mesophase domains as a physical effect. The analysis of the resulting cokes by scanning electron microscopy (SEM) showed that catalyst particles agglomerated and stuck to the outer surface of the mesophase domains and suppressed their coalescence. The agglomeration of catalyst particles likely decreased their ability to suppress the formation of small mesophase domains, in the range of a few micrometers in size. However, catalyst was effective in suppressing the formation of bulk mesophase domains with areas over 2000μm~2. The results showed that the onset of observable mesophase initially increased with the addition of catalyst, but then decreased at higher catalyst concentrations. SEM observation confirmed that the significant agglomeration of catalyst particles at higher concentrations was likely responsible for the decreased effectiveness of the catalyst in suppressing mesophase formation.
机译:使用具有视图窗口和搅拌器的微反应器观察Athabasca真空残留物中的中间相形成,并且没有催化剂在4.8MPa下的真空残留情况下,研究了在4.8MPa下的真空残留情况下搅拌对中间相形成及其生长和聚结的效果。 440°C。搅拌可导致中间体结构域的尺寸的双峰分布。搅拌器的中间相液滴的强制聚结会导致形成非常大的中间相区域(块状中间相),其与大量小的微米尺寸的中间相结构相同。催化剂的添加可能对中间相的形成和生长具有化学和物理效应。催化剂在中间相形成的延迟中,作为化学效果,通过抑制较小中间体域的聚结会作为物理效应来降低块状中间相区域的减少。通过扫描电子显微镜(SEM)的所得焦炭的分析显示催化剂颗粒附聚并粘附到中间体结构域的外表面并抑制它们的聚结。催化剂颗粒的凝聚可能降低了它们抑制小中间体域的形成的能力,在尺寸的几微米的范围内。然而,催化剂有效地抑制块状中间体结构域的形成,其中具有超过200μm〜2的区域。结果表明,可观察到的中间相开始随着催化剂的添加而最初增加,但随后在较高的催化剂浓度下降低。 SEM观察证实,催化剂颗粒在较高浓度下的显着凝聚可能是催化剂在抑制中间相形成时的有效性降低。

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