Catalytic steam reforming of simulated bio-oil for green hydrogen production using highly active LaNixCo1-xO3 perovskite catalyst

Catalytic steam reforming (SR) of agricultural waste derived bio-oil for hydrogen production is a unique technology, offering twin benefits of waste management as well as sustainable energy production. In the...

VOC and CO Removals by Perovskite Type Nanocatalysts Supported on Commercial Substrates

In this research, it was tried to choose a kind of perovskite catalyst with optimized formulation La0.8Sr0.2Co0.66Fe0.34O3 to remove air pollutants. This perovskite catalyst stabilized on the various supports such as alumina and ZSM-5 with the sol-gel synthesis technique and ceramic monolith by dip-coating method. Four different catalysts by variable weight percentage including PE-Al 10%, PE-Al 20%, PE-Al 30%, and PE-Al 40% were prepared by sol-gel synthesis technique. In this work, the XRD technique was used to confirm the formation of perovskite catalysts’ crystalline phases on the supports. As a result, XRD patterns revealed the formation of the perovskite phase onto the alumina and zeolite supports. Activity tests of these four catalysts were examined in the catalytic oxidation of Toluene and CO using an experimental setup consisting of a tubular flow reactor at the temperature 280-400°C and 100-400°C for the toluene and CO removal systems, respectively. According to the results of the catalysts’ activity test, the alumina supported with 40% w/w perovskite catalyst showed the best performance, and its activity was similar to the activity of the bulk catalyst (over 95% conversion of toluene at about 290°C). For the coated catalysts on a ceramic monolith, the complete removal of carbon monoxide at 50°C was lower than the powdered form. Results from the activity test in a toluene removal system that show coating of the bulk and supported catalysts on ceramic monolith; have an essential impact on the activity test of these catalysts.

Alkaline modified A-site deficient perovskite catalyst surface with exsolved nanoparticles and functionality in biomass valorisation

Environmental problems associated with the use of fossil fuels and increase in energy demands due to rise in population and rapid industrialisation, are the driving forces for energy. Catalytic conversion of biomass to renewable energies is among the promising approaches to materialize the above. This requires development of robust catalysts to suppress deactivation due to carbon deposition and agglomeration. In this work, surface properties and chemistry such as exsolution of B-site metal catalyst nanoparticles, particle size and distribution, as well as catalyst-support interactions were tailored through the use of alkaline dopants to enhance catalytic behaviour in valorisation of glycerol. The incorporation of alkaline metals into the lattice of an A-site deficient perovskite modified the surface basic properties and morphology with a consequent robust catalyst-support interaction. This resulted in promising catalytic behaviour of the materials where hydrogen selectivity of over 30% and CO selectivity of over 60% were observed. The catalyst ability to reduce fouling of the catalyst surface as a result of carbon deposition during operation was also profound due to the robust catalyst-support interaction occurring at the exsolved nanoparticles due to their socketing and the synergy between the dopant metals in the alloy in perovskite catalyst systems. In particular, one of the designed systems, La0.4Sr0.2Ca0.3Ni0.1Ti0.9O3±δ, displayed almost 100% resistance to carbon deposition. Therefore, lattice rearrangement using exsolution and choice of suitable dopant could be tailored to improve catalytic performance.