Renewable Hydrogen Production from Butanol Steam Reforming over Nickel Catalysts Promoted by Lanthanides

Hydrogen is mainly produced by steam reforming of natural gas, a nonrenewable resource. Alternative and renewable routes for hydrogen production play an important role in reducing dependence on oil and minimizing the emission of greenhouse gases. In this work, butanol, a model compound of bio-oil, was employed for hydrogen production by steam reforming. The reaction was evaluated for 30 h in a tubular quartz reactor at 500 °C, atmospheric pressure, GHSV of 500,000 h−1, and an aqueous solution feed of 10% v/v butanol. For this reaction, catalysts with 20 wt.% NiO were prepared by wet impregnation using three supports: γ-alumina and alumina modified with 10 wt.% of cerium and lanthanum oxides. Both promoters increased the reduction degree of the catalysts and decreased catalyst acidity, which is closely related to coke formation and deactivation. Ni/La2O3–Al2O3 presented a higher nickel dispersion (14.6%) which, combined with other properties, led to a higher stability, higher mean hydrogen yield (71%), and lower coke formation per mass (56%). On the other hand, the nonpromoted catalyst suffered a significant deactivation associated with coke formation favored by its highest acidity (3.1 µmol m−²).

Preparation of Nanosized LaCoO3through Calcination of a Hydrothermally Synthesized Precursor

A method for obtaining nanosized LaCoO3crystals from calcination of a precursor powder synthesized by a hydrothermal route is reported. Details concerning the evolution of the microstructure and formation mechanism of the perovskite phase were studied by powder X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy, Raman spectroscopy, and thermal analysis. It was found that the morphology of the sample progressively turns from a mix of fibers and rods to interconnected nanocrystals. It is determined that LaCoO3phase is produced by a reaction of cobalt and lanthanum oxides, the latter produced by a two-step dehydration process of La(OH)3. Finally, it was found that nearly stoichiometric LaCoO3nanocrystals can be obtained at temperatures as low as 850°C. Nevertheless, whether higher calcination temperatures are used, appropriate reaction times and a controlled atmosphere are required in order to avoid formation of lanthanum carbonates and high density of lattice defects.