首页> 外文期刊>Journal of Analytical & Applied Pyrolysis >Synthesis course and surface properties of praseodymium oxide obtained via thermal decomposition of praseodymium acetate: Impacts of the decomposition atmosphere
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Synthesis course and surface properties of praseodymium oxide obtained via thermal decomposition of praseodymium acetate: Impacts of the decomposition atmosphere

机译:乙酸热分解制得的氧化oxide的合成过程和表面性质:分解气氛的影响

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The decomposition course, intermediates and final products of praseodymium acetate monohydrate Pr(CH_3COO)_3·H_2O in different gas atmospheres (O_2, N_2 or H_2) were characterized using thermal analysis, X-ray diffractometry and infrared spectroscopy. Praseodymium acetate decomposes in five mass loss events leading to the formation of the intermediate products Pr(OH)(CH_3COO)_2, PrO(CH_3COO) and Pr_2O_2CO_3. Results obtained indicate that praseodymium acetate decomposes into a number of intermediate products whose chemical structure is independent on the gas atmosphere applied, but the kinetics of their formation and subsequent decomposition is considerably enhanced in O_2 atmosphere. The final product at 700℃ was found to be praseodymium oxide Pr_6O_(11) in O_2 and N_2, but mixed with minority Pr_2O_3 in H_2 atmosphere. Surface texture and 2-propanol decomposition activity of the final products at 700℃ were determined by means of N_2 sorptiometry and in situ IR spectroscopy. The final products in O_2 and N_2 were slightly more active catalysts toward 2-propanol decomposition the latter was of higher selectivity toward the alcohol dehydration, which is suggested to be correlated with the evolution of a narrower mesoporous structure on its surface.
机译:利用热分析,X射线衍射和红外光谱对一氧化acetate水合物Pr(CH_3COO)_3·H_2O在不同气体气氛(O_2,N_2或H_2)中的分解过程,中间体和终产物进行了表征。乙酸在五个质量损失事件中分解,导致形成中间产物Pr(OH)(CH_3COO)_2,PrO(CH_3COO)和Pr_2O_2CO_3。所得结果表明,乙酸s分解成许多中间产物,其化学结构与所施加的气体气氛无关,但是在O_2气氛中,它们的形成动力学和随后的分解动力学大大增强。 700℃时的最终产物在O_2和N_2中为氧化oxidePr_6O_(11),但在H_2气氛中与少数Pr_2O_3混合。用N_2吸光光度法和原位红外光谱法测定了700℃时最终产物的表面织构和2-丙醇分解活性。 O_2和N_2中的最终产物是对2-丙醇分解的活性更高的催化剂,而后者对醇类脱水的选择性更高,这被认为与表面较窄的介孔结构的演变有关。

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