A theoretical model is proposed for the quantitative description of the chronopotentiometric (E-t) responses, under galvanostatic control, of either conducting polymer films or dual sensing-actuating devices. Assuming that the reaction occurs by extraction, or injection, of n consecutive electrons from, or to, a polymer chain the material moves through n consecutive oxidation or reduction states. Stair functions are obtained describing either potential or consumed electrical energy evolutions as a function of both, driving (current) and environmental (temperature, electrolyte concentration...) variables. The current quantifies the actuation of any electrochemical device (charge/discharge of batteries, movement rate, and position of muscles): the stair functions are dual actuating-sensing functions. A good agreement exists between theoretical and experimental results from either polypyrrole films or artificial muscles at different temperatures. Only two connecting wires include, at any time, sensing (potential) and working (current) information of any dual device.

International audienceA novel CeO2/MgO catalyst with low ceria loading has been synthesized. This catalyst showed unique redox properties compared with conventional high and low surface area CeO2. Advanced (scanning) transmission electron microscopy techniques revealed the presence of a variety of highly dispersed ceria nanostructures: isolated CeOx entities, CeO2 clusters, as well as fairly small (<5nm) CeO2 nanoparticles. More interestingly, this CeO2/MgO catalyst showed outstanding stability in its redox response against high temperature aging treatments. Thus, after reduction in hydrogen at 950 degrees C and further oxidation at 500 degrees C, CeO2 reduction effects took still place at low temperatures, and no significant loss of oxygen storage capacity (OSC) was detected. Unique ceria-bilayer nanostructures were found and characterized in the aged catalyst. Their peculiar structural and chemical properties seem to be responsible for the large improvement observed in the stability of the redox response

Ketobutenolide 3, easily obtained from santonin (1), has been transformed into two natural furanoeudesmanes 4 and 5, isolated from Commiphora molmol and Tubipora musica, respectively. trans- And cis-decalin systems were obtained by stereoselective reduction of the C(4)-C(5) double bond in 3 in the following way: hydrogenation of 3 over Pd/C followed by acidic treatment gave the cis isomer 10 as the major product; selective hydrogenation of the C(1)-C(2) double bond with the Wilkinson's catalyst followed by reduction with NaTeH yielded mainly the trans isomer 9. Compounds 9 and 10 were transformed into 4 and 5 in parallel sequences. Optical rotation and CD measurements of the synthetic products revealed that the stereochemistry of both natural products should be revised to their enantiomeric form.

A very low loading mixed CeO2–TbOx catalyst, supported on MgO, with improved methane total oxidation activity and stability.

Biofouling frequently involves a serious impediment to achieving optimum operating conditions in heat exchangers-condensers. The economic coat and energy losses associated with this phenomenon are significant and the environmental impact of biocides must satisfy stringent regulations. A portable pilot plant has been designed in order to carry out in-situ experimental study as biofilm is formed under thermal and hydrodynamically controlled conditions. The pilot plant has an automatic monitoring, control and data acquisition system, which automatically processes data from indirect measure of fouling in terms of increased fluid frictional and heat transfer resistances. A particular method is used and proposed for direct measuring and biofilm characterization. Once we know the actual film thickness, we can calculate the effective thermal conductivity of the layer by using the appropriate heat transfer equations.