Brief Review of Precipitated Iron-Based Catalysts for Low-Temperature Fischer–Tropsch Synthesis

Topics in Catalysis - Fischer–Tropsch synthesis (FTS) is a promising way to produce clean liquid fuels and high value-added chemicals from low-value carbon-containing resources such as coal,...     

Phase-controlled synthesis of thermally stable nitrogen-doped carbon supported iron catalysts for highly efficient Fischer-Tropsch synthesis

Nano Research - Iron-based nanoparticles with uniform and high particle dispersion, which are supported on carbon structures, have been used for various applications. However, their preparation...     

Preparation of Cu/ZnO catalyst using a polyol method for alcohol-assisted low temperature methanol synthesis from syngas

A polyol method was used to prepare Cu/ZnO catalysts for alcohol-assisted low temperature methanol synthesis from syngas. Unlike conventional low temperature methanol synthesis, ethanol was employed both as a solvent and a reaction intermediate. Catalyst characterization revealed that Cu/ZnO catalysts were successfully and efficiently prepared using the polyol method. Various preparation conditions such as PVP concentration and identity of ZnO precursor strongly influenced the catalytic activity of Cu/ZnO catalysts. Copper dispersion and catalyst morphology played key roles in determining the catalytic performance of the Cu/ZnO catalyst in alcohol-assisted low temperature methanol synthesis. A high copper dispersion and platelike Cu/ZnO structure led to high catalytic activity. Among the catalysts tested, 5_Cu/ZnO_Zn(Ac)₂ had the best catalytic performance due to its high copper dispersion.     

Hydrogen evolution performance of magnesium alanate prepared by a mechanochemical metathesis reaction method

Solvent-free magnesium alanates were prepared by a mechanochemical metathesis reaction method (ball milling method) with a variation of milling time. For the purpose of comparison, magnesium alanate was also prepared by metathesis reaction method in the presence of diethyl ether. The formation of magnesium alanate (Mg(AlH₄)₂) and magnesium alanate-diethyl ether (Mg(AlH₄)₂·Et₂O) adduct was confirmed by XRD measurements. In both magnesium alanates, hydrogen evolution occurred in the first step decomposition. The starting temperature for hydrogen evolution of the solvent-free magnesium alanates decreased with increasing milling time, whereas the amount of hydrogen evolution of the solvent-free magnesium alanates increased with increasing milling time. The maximum amount of hydrogen evolution of the Mg(AlH₄)₂·Et₂O adduct was slightly larger than that of the solvent-free Mg(AlH₄)₂, but the starting temperature for hydrogen evolution of the Mg(AlH₄)₂·Et₂O adduct was much higher than that of the solvent-free Mg(AlH₄)₂. The addition of a small amount of titanium to the solvent-free Mg(AlH₄)₂ greatly reduced the hydrogen evolution temperature of titanium-doped Mg(AlH₄)₂. However, the maximum amount of hydrogen evolution of the titanium-doped Mg(AlH₄)₂ was smaller than that of the solvent-free Mg(AlH₄)₂.