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Synthesis of zirconium oxycarbide powders using metal-organic framework (MOF) compounds as precursors

机译:以金属有机骨架化合物为前驱体合成碳氧化锆粉末

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摘要

ZrCxOy oxycarbides were synthesized for the first time by using metal-organic framework (MOF) compounds as precursors. These MOFs, based on zirconium carboxylates, are derived from the UiO-66 type structure. Three different Zr-MOF compounds were synthesized, differing by their C/Zr ratio, due to the use of terephthalic acid (C/Zr = 8, or UiO-66), naphthalene-2,6-dicarboxylic acid (C/Zr = 12) and biphenyl-4,40-dicarboxylic acid (C/Zr = 14 or UiO-67). The oxycarbide crystallites obtained through appropriate thermal treatments (under Ar atmosphere) of the Zr-MOF precursors show an average size of a few hundred microns. They are surrounded by an outer rim of turbostratic carbon, whose thickness is directly relevant to the C/Zr ratio coming from the nature of the organic linker. The composition of the oxycarbides obtained was estimated on the basis of the cell parameters refined from the powder XRD patterns. The oxycarbides synthesized from naphtalene-2,6-dicarboxylic acid and biphenyl-4,40-dicarboxylic acid are close to ZrC0.925O0.075, while that of the oxycarbide obtained from the terephthalic acid precursor is ZrC0.944O0.056. It results that the carbon richer oxycarbide product is observed for the UiO-66 precursor synthesized with terephthalic acid, and exhibiting the lower C/Zr ratio of the series. The composition of the oxycarbide powders is shown to be directly relevant to the mechanisms of decomposition of the Zr-MOF compound involved during heating.
机译:以金属有机骨架(MOF)化合物为前体,首次合成了ZrCxOy碳氧化物。这些基于羧酸锆的MOF衍生自UiO-66型结构。由于使用了对苯二甲酸(C / Zr = 8或UiO-66),萘-2,6-二羧酸(C / Zr =),因此合成了三种不同的Zr-MOF化合物,它们的C / Zr比不同。 12)和联苯-4,40-二羧酸(C / Zr = 14或UiO-67)。通过对Zr-MOF前体进行适当的热处理(在Ar气氛下)获得的碳氧化物微晶的平均尺寸为几百微米。它们被涡轮层碳的外缘包围,其厚度与有机连接基的性质与C / Zr比直接相关。根据从粉末XRD图谱提炼的晶胞参数,估算得到的碳氧化物的组成。由萘-2,6-二羧酸和联苯-4,40-二羧酸合成的碳氧化物接近ZrC0.925O0.075,而由对苯二甲酸前体获得的碳氧化物为ZrC0.944O0.056。结果表明,用对苯二甲酸合成的UiO-66前驱体观察到了富碳的碳氧化物产物,并显示出较低的C / Zr比。碳氧化物粉末的组成显示出与加热期间所涉及的Zr-MOF化合物的分解机理直接相关。

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