The Effect of Atomic Layer Deposited Overcoat on Co-Pt-Si/γ-Al2O3 Fischer–Tropsch Catalyst

Atomic layer deposition (ALD) was used to prepare a thin alumina layer on Fischer–Tropsch catalysts. Co-Pt-Si/γ-Al2O3 catalyst was overcoated with 15–40 cycles of Al2O3 deposited from trimethylaluminum (TMA) and water vapor, followed by thermal annealing. The resulting tailored Fischer–Tropsch catalyst with 35 cycle ALD overcoating had increased activity compared to unmodified catalyst. The increase in activity was achieved without significant loss of selectivity towards heavier hydrocarbons. Altered catalyst properties were assumed to result from cobalt particle stabilization by ALD alumina overcoating and nanoscale porosity of the overcoating. In addition to optimal thickness of the overcoat, thermal annealing was an essential part of preparing ALD overcoated catalyst.

High performance cobalt nanoparticle catalysts supported by carbon for ozone decomposition: the effects of the cobalt particle size and hydrophobic carbon support

Catalytic gaseous ozone decomposition under high humidity is not only an urgent need but also a significant challenge because of the low stability over the available catalysts.

Stability of cobalt-based Fischer–Tropsch catalyst supported on oxidized carbon nanotubes

The stability of 20[Formula: see text]wt.% Co/CNT catalyst was tested in the Fischer–Tropsch synthesis and the structural transformations both in the catalyst and support were analyzed. The catalyst showed high conversion and stable selectivity during three weeks of the test, which was attributed to the optimal and stable cobalt particle size of [Formula: see text]13–14[Formula: see text]nm promoted by the support pre-oxidation. XPS, Raman, and nitrogen adsorption data revealed that the carefully chosen catalyst annealing and reduction conditions ensured the preservation of the support structure.

Cobalt-based Fischer–Tropsch catalysts supported on different types of N-doped carbon nanotubes

N-doped nanocarbons are promising materials for metal-free and supported catalysts. Three types of N-doped carbon nanotubes (N-CNTs) were synthesized by chemical vapor deposition (CVD), by oxidation of the CVD produced N-CNTs with nitric acid, and by post-doping of oxidized undoped CNTs with ammonia. Cobalt catalysts with 20[Formula: see text]wt.% loading supported on N-CNTs were tested in the Fischer–Tropsch synthesis. Oxidized N-CNTs containing pyridone groups demonstrated the best stabilization of cobalt nanoparticles. The catalyst on this support showed the highest selectivity towards [Formula: see text] hydrocarbons. The performance of the catalyst supported on CVD N-CNTs was the worst because of the large variation in cobalt particle size and low reduction degree. The catalysts supported on post-doped CNTs demonstrated the best activity, but high methane selectivity because of the low Co particle size ([Formula: see text][Formula: see text]nm).

The Effect of Potassium on Cobalt-Based Fischer–Tropsch Catalysts with Different Cobalt Particle Sizes

The effect of K on 20%Co/0.5%Re/γ-Al2O3 Fischer–Tropsch catalysts with two different cobalt particle sizes (small, in the range 6–7 nm and medium size, in the range 12–13 nm) was investigated. The catalyst with the smaller cobalt particle size had a lower catalytic activity and C5+ selectivity while selectivities towards CH4 and CO2 were slightly higher than over the catalyst with larger particles. These effects are ascribed to lower hydrogen concentration on the surface as well as the lower reducibility of smaller cobalt particles. Upon potassium addition all samples showed decreased catalytic activity, reported as Site Time Yield (STY), increased C5+ and CO2 selectivities, and a decrease in CH4 selectivity. There was no difference in the effect of potassium between the sample with small cobalt particles compared to the sample with medium size particles). In both cases the specific activity (STY) fell and the C5+ selectivity increased in a similar fashion.

Nitrogen doping as a fundamental way to enhance the EMI shielding behavior of cobalt particle-embedded carbonaceous nanostructures

The influence of nitrogen doping in pyrolysis-derived carbonaceous nanostructures with embedded Co-nanoparticles (Co@C) for electromagnetic (EM) absorption at microwave frequencies is explored.

Structure-, dimension-, and particle size-engineering toward highly efficient supported nanoparticulate metal catalysts

Among the nitrogen doped carbon-supported nanoparticulate cobalt catalysts of different dimensions and cobalt particle sizes screened, 2D Co–N–C-0.5 is identified as the most efficient catalyst.