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Nanostructured Ni/CeO2-ZrO2 Catalysts for CO2 Conversion into Synthetic Natural Gas

机译:纳米结构Ni / CeO 2-ZrO2催化剂的CO2转化为合成天然气

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NiO-CeO2-ZrO2 mixed oxides, with Ni/(Ce + Zr) = 1 mol/mol and different Ce/Zr molar ratios, were prepared by the soft-template method. The chemical composition, texture, structure, and redox features of the synthesized systems were investigated by different techniques. All samples were nanocrystalline (NiO nanocrystal average size 4 nm) and had high surface area and quite an ordered mesoporous system. The catalytic performances in the CO2 conversion into methane were studied at atmospheric pressure, 300 degrees C, and stoichiometric H-2/CO2 molar ratio. Prior to reaction the catalysts were submitted to a mild reduction pretreatment (H-2 at 400 degrees C for 1 h). XRD analysis of the samples after pretreatment showed the presence of small Ni crystals (4-7 nm) on all the samples as well as of some unreduced NiO nanocrystals on the systems with high Zr content, in accordance with H-2-TPR experiments, which indicated that NiO reduction is promoted by CeO2 but hindered by ZrO2. The catalytic tests were performed at two different space velocities (72000 and 900000 cm(3) h(-1) g(cat)(-1)) on a series of Ni-based catalysts supported on CeO2-ZrO2 systems with different Ce/Zr ratios, including the two pure oxides. CO2 conversion and selectivity to CH4 (which was always close to 100 mol%) were constant throughout the 6-hour runs. CO2 conversion resulted to increase with CeO2 content in the catalyst, thus indicating the role of the CeO2 component of the support in activating CO2, whereas H-2 is activated on the Ni nanoparticles.
机译:通过软模板法制备NiO-CeO2-ZrO2混合氧化物,具有Ni /(Ce + Zr)= 1mol / mol和不同的Ce / Zr摩尔比。通过不同的技术研究了合成系统的化学成分,质地,结构和氧化还原特征。所有样品均为纳米晶(NiO纳米晶体平均4nm),具有高表面积和相当有序的介孔系统。在大气压,300℃和化学计量的H-2 / CO2摩尔比下研究CO 2转化为甲烷中的催化性能。在反应之前,将催化剂提交至温和的降低预处理(在400℃下的H-2持续1小时)。预处理后样品的XRD分析显示所有样品上的小Ni晶体(4-7nm)以及根据H-2-TPR实验,在具有高Zr含量的系统上的一些未发育的NiO纳米晶体中的存在,这表明通过CEO2促进了NIO减少,但受ZRO2阻碍。催化试验在两种不同的空速(72000和900000cm(3)H(-1)g(猫)( - 1))上进行,在一系列基于Ni的基于CEO2-ZrO2系统上的基于Ni的催化剂上,具有不同的CE / Zr比率,包括两个纯氧化物。在整个6小时的运行过程中,CO 2转化和选择性对CH4(总是接近100mol%)的恒定。 CO 2转化导致催化剂中的CeO 2含量增加,从而表明CeO2组分在活化CO 2中的作用,而H-2在Ni纳米颗粒上被活化。

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