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首页> 外文期刊>International journal of hydrogen energy >Synthesis and characterization of magnetic zinc and manganese ferrite catalysts for decomposition of carbon dioxide into methane
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Synthesis and characterization of magnetic zinc and manganese ferrite catalysts for decomposition of carbon dioxide into methane

机译:磁性锌锰铁氧体催化剂的合成与表征,用于将二氧化碳分解为甲烷

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Recently, carbon dioxide (CO2) has been regarded as the main source of greenhouse gases in the world with global warming potential. Decomposition or methanation of CO2 with flowing H-2 over oxygen -deficient ZnFe2O4 and MnFe2O4 nanocatalysts at 300-400 degrees C and 1 atm was studied. Fine structures of Fe/Zn/Mn species in ZnFe2O4/MnFe2O4 were also investigated. Experimentally, as -synthesized ZnFe2O4./MnFe2O4 nanocatalysts were prepared by a hydrothermal method for CO2 decomposition or methanation. Oxygen deficiency of ZnFe2O4/MnFe2O4 was obtained by reduction in hydrogen gas. Decomposition of CO2 into C and O-2 was carried out within few minutes when it comes into contact with oxygen -deficient ZnFe2O4/MnFe2O4 through incorporation of O-2 into ferrites. Oxygen and carbon rather than CO were produced in the decomposition process. The complete decomposition of CO2 was possible due to higher degree of oxygen deficiency. The pre-edge XANES spectra of fie atom in ZnFe2O4/MnFe2O4 exhibits an absorbance feature at 7115 eV for the 1s to 3d transition which is forbidden by the selection rule in case of perfect octahedral symmetry. The EXAFS data showed that ZnFe2O4 (MnFe2O4) catalyst had two central Fe atoms coordinated by primarily Fe O with a bond distance of 2.07 +/- 0.02 (1.95 +/- 0.02) with a coordination number of 3.94 (4.07), respectively. CH4 was produced during the reactivation of ZnFe2O4/MnFe2O4 with H2. Moreover, kinetics and thermodynamics studies of CO2 decomposition and methanation over ZnFe2O4/MnFe2O4 at 300-400 degrees C and 1 atm were also calculated using pseudo first-order model and Arrhenius equation, respectively. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:最近,二氧化碳(CO2)已被视为具有全球变暖潜力的世界上主要的温室气体源。研究了在缺氧的ZnFe2O4和MnFe2O4纳米催化剂上在300-400摄氏度和1个大气压下用流动的H-2对CO2进行分解或甲烷化的过程。还研究了ZnFe2O4 / MnFe2O4中Fe / Zn / Mn的精细结构。实验上,通过水热法制备了合成的ZnFe2O4./MnFe2O4纳米催化剂,用于CO2分解或甲烷化。 ZnFe2O4 / MnFe2O4的氧气不足是通过还原氢气获得的。通过将O-2掺入铁氧体中,使其与缺氧的ZnFe2O4 / MnFe2O4接触,在几分钟内将CO2分解为C和O-2。在分解过程中会产生氧气和碳,而不是一氧化碳。由于更高程度的缺氧,CO2可能完全分解。 ZnFe2O4 / MnFe2O4中原子原子的前缘XANES光谱在7115 eV处具有1s到3d跃迁的吸光度特征,这在完全八面体对称的情况下是选择规则所禁止的。 EXAFS数据显示,ZnFe2O4(MnFe2O4)催化剂具有两个主要由Fe O配位的中心Fe原子,其键距分别为2.07 +/- 0.02(1.95 +/- 0.02),配位数为3.94(4.07)。在用H2活化ZnFe2O4 / MnFe2O4的过程中产生CH4。此外,还分别使用伪一阶模型和Arrhenius方程计算了ZnFe2O4 / MnFe2O4在300-400摄氏度和1 atm下CO2分解和甲烷化的动力学和热力学研究。 (C)2017氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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