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Heterogeneously catalysed partial oxidation of acrolein to acrylic acid - structure, function and dynamics of the V/Mo/W mixed oxides

机译:丙烯醛非均相催化部分氧化为丙烯酸-V / Mo / W混合氧化物的结构,功能和动力学

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摘要

The major objective of this research project was to reach a microscopic understanding of the structure, function and dynamics of V-Mo-(W) mixed oxides for the partial oxidation of acrolein to acrylic acid. Different model catalysts (from binary and ternary vanadium molybdenum oxides up to quaternary oxides with additional tungsten) were prepared via a solid state preparation route and hydrochemical preparation of precursors by spray-drying or crystallisation with subsequent calcination. The phase composition was investigated ex situ by XRD and HR-TEM. Solid state prepared samples are characterised by crystalline phases associated to suitable phase diagrams. Samples prepared from crystallised and spray-dried precursors show crystalline phases which are not part of the phase diagram. Amorphous or nanocrystalline structures are only found in tungsten doped samples. The kinetics of the partial oxidation as well as the catalysts' structure have been studied in situ by XAS, XRD, temperature programmed reaction and reduction as well as by a transient isotopic tracing technique (SSITKA). The reduction and re-oxidation kinetics of the bulk phase have been evaluated by XAS. A direct influence not only of the catalysts' composition but also of the preparation route is shown. Altogether correlations are drawn between structure, oxygen dynamics and the catalytic performance in terms of activity, selectivity and long-term stability. A model for the solid state behaviour under reaction conditions has been developed. Furthermore, isotope exchange experiments provided a closer image of the mechanism of the selective acrolein oxidation. Based on the in situ characterisation in combination with micro kinetic modelling a detailed reaction model which describes the oxygen exchange and the processes at the catalyst more precisely is discussed.
机译:该研究项目的主要目的是从微观上了解用于将丙烯醛部分氧化为丙烯酸的V-Mo-(W)混合氧化物的结构,功能和动力学。通过固态制备路线和通过喷雾干燥或结晶以及随后的煅烧进行前体的水化学制备,制备了不同的模型催化剂(从二元和三元钒钼氧化物到具有额外钨的四元氧化物)。相组成通过XRD和HR-TEM异位研究。固态制备的样品的特征在于与合适的相图相关的结晶相。由结晶和喷雾干燥的前驱体制备的样品显示的晶相不属于相图。非晶或纳米晶体结构仅在钨掺杂的样品中发现。通过XAS,XRD,程序升温反应和还原以及瞬态同位素示踪技术(SSITKA)对原位氧化的动力学以及催化剂的结构进行了研究。 XAS已评估了本体相的还原和再氧化动力学。不仅示出了催化剂组成的直接影响,而且还示出了制备路线的直接影响。根据活性,选择性和长期稳定性,在结构,氧动力学和催化性能之间共绘制了相关性。已经开发了反应条件下固态行为的模型。此外,同位素交换实验提供了选择性丙烯醛氧化机理的更详尽的图像。基于原位表征并结合微观动力学模型,讨论了详细的反应模型,该模型更精确地描述了氧的交换和在催化剂上的过程。

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