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STRUCTURE EVOLUTION OF CuFe BIMETALLIC NANOPARTICLE FOR HIGHER ALCOHOLS SYNTHESIS

机译:高脂金属纳米粒子对较高醇合成的结构演变

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Higher alcohols synthesis (HAS) via syngas has attracted much attention from both industry and academia due to their application as fuel, fuel additives and intermediates for value-added chemicals. Many catalysts have been reported for HAS via syngas and the typical ones include modified methanol catalysts, Rh based catalysts, molybdenum based catalysts, and modified Fischer-Tropsch (F-T) catalysts. Among them, the Cu modified F-T catalysts have been considered as one of the most promising catalysts. However, largescale industrial application for Cu modified F-T catalysts is not available due to the poor stability in long-term run and the low total alcohol selectivity from the practical point of view. Courty et al proposed that the separation of Co (F-T component) from the originally homogeneously distributed Cu-Co phases might be one of the reasons that caused the decrease of alcohol selectivity. Previously, we found the CuFe bimetallic nanoparticle is promising catalyst for HAS especially for C6~+OH synthesis. Herein, the structure evolution of CuFe bimetallic nanoparticle during HAS process was studied in detail. In addition, the correlation of the change of catalytic performance with the structure evolution was also investigated to reveal the nature of deactivation mechanism of CuFe nanocatalysts. The separation of Cu and Fe components was directly observed, and was responsible to decreased alcohol selectivity.
机译:由于其应用作为增值化学品的燃料,燃料添加剂和中间体,通过合成气的较高醇合成(已经)引起了工业和学术界的许多关注。已经报道了通过合成气的许多催化剂,并且典型的催化剂包括改性的甲醇催化剂,Rh基催化剂,基于钼基催化剂和改性的Fischer-Tropsch(F-T)催化剂。其中,Cu改性的F-T催化剂被认为是最有前途的催化剂之一。然而,由于在实际观点来看,由于长期运行的稳定性差和较低的总酒精选择性而无法获得Cu改性F-T催化剂的大型工业应用。 Courty等人提出,来自最初均匀分布的Cu-Co阶段的CO(F-T组分)的分离可能是导致醇选择性降低的原因之一。以前,我们发现Cufe双金属纳米粒子是有前途的催化剂,特别是对于C6〜+ OH合成。这里,详细研究了Cufe双金属纳米粒子的结构演化。此外,还研究了催化性能变化与结构演化的改变,以揭示CUFE纳米催化剂的失活机制的性质。直接观察到Cu和Fe组分的分离,并负责降低醇选择性。

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