Sustainable Hydrogen from Bio-Oil - Catalytic Steam Reforming of Acetic Acid as a Model Oxygenate

Studies were conducted with acetic acid (HAc) as model oxygenate for the design of active and stable catalysts for steam reforming of bio-oil. Pt/ZrO2 catalysts were prepared by wet impregnation technique. The Pt/ZrO2 catalysts showed high activities at initial time on stream, but lost its activity for steam reforming (H2 production) rapidly. During HAc/H2O reaction over Pt/ZrO2, conversion was close to 100% and constant for 3 hr, however, yields of products changed with time. In the beginning (5 min), H2 and CO2 were the main products, CH4 and CO were observed in small quantities. During HAc/H2O reaction over ZrO2 (without Pt), HAc conversion was close to 90%. The conversion of HAc and yields of the products were constant for 3 hr. However, no steam reforming activity (H2 and CO) was observed, and only acetone and CO2 were observed as products. Both Pt/ZrO2 and ZrO2 were very active for HAc conversion. However, H2 and CO, i.e., steam reforming products, were produced only over Pt/ZrO2 and not over ZrO2. ZrO2 showed acetone yields similar to those observed over Pt/ZrO2 after 25 min time on stream. The presence of acetone in the product mixture and formation of deposits on ZrO2 indicated a role for acetone in catalyst deactivation

Building micro-soccer-balls with evaporating colloidal fakir drops

Evaporation-driven particle self-assembly can be used to generate three-dimensional microstructures. We present a new method to create these colloidal microstructures, in which we can control the amount of particles and their packing fraction. To this end, we evaporate colloidal dispersion droplets on a special type of superhydrophobic micro-structured surface, on which the droplet re- mains in Cassie-Baxter state during the entire evaporative process. The remainders of the droplet consist of a massive spherical cluster of the microspheres, with diameters ranging from a few tens up to several hundreds of microns. We present scaling arguments to show how the final particle packing fraction of these balls depends on the dynamics of the droplet evaporation.Comment: Manuscript Submitted to Physical Review Letters, 29th February 201

On-chip microplasma reactors using carbon nanofibres and tungsten oxide nanowires as electrodes

Carbon nanofibres (CNFs) and tungsten oxide (W18O49) nanowires have been incorporated into a continuous flow type microplasma reactor to increase the reactivity and efficiency of the barrier discharge at atmospheric pressure. CNFs and tungsten oxide nanowires were characterized by high-resolution scanning electron microscopy, transmission electron microscopy and nanodiffraction methods. Field emission of electrons from those nanostructures supplies free electrons and ions during microplasma production. Reduction in breakdown voltage, higher number of microdischarges and higher energy deposition were observed at the same applied voltage when compared with plane electrodes at atmospheric pressure in air. Rate coefficients of electron impact reaction channels to decompose CO2 were calculated and it was shown that CO2 consumption increased using CNFs compared with plane electrode in the microplasma reactor