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首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Electron spectroscopy of sulfated zirconia, its activity in n-hexane conversion and possible reasons of its deactivation
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Electron spectroscopy of sulfated zirconia, its activity in n-hexane conversion and possible reasons of its deactivation

机译:硫酸氧化锆的电子光谱,其在正己烷转化中的活性及其失活的可能原因

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Sulfated zirconia catalyst were prepared and characterized by X-ray photoelectron spectroscopy taken in the dried state (fresh) and after calcination at 900 K (calc.)A maximum activity was observed as a function of the calcination temperature. The Zr 3d region showed that any Zr hydroxide in the dried catalyst transformed into zirconium oxide upon calcination. The O 1s peak could be fitted by two components corresponding to ZrO_2 and sulfate, respectively. Sulfur was present as sulfate. Both catalysts showed activity in n-hexane conversion (including isomerization) between 300 and 473 K. The activity of the calcined catalyst was much higher. The main products were isopentane and isobutane, along with 2-methyl-and 3-methylpentane.
机译:制备了硫酸化的氧化锆催化剂,并通过X射线光电子能谱表征,以干燥状态(新鲜)和在900 K(计算)下煅烧后观察到的最大活性随煅烧温度的变化而变化。 Zr 3d区域显示,在煅烧后,干燥催化剂中的任何Zr氢氧化物都转化为氧化锆。 O 1s峰可以由分别对应于ZrO_2和硫酸盐的两个组分拟合。硫以硫酸盐形式存在。两种催化剂都显示出在300至473 K之间的正己烷转化率(包括异构化)活性。煅烧催化剂的活性高得多。主要产物是异戊烷和异丁烷,以及2-甲基和3-甲基戊烷。

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