Sustainable Recycling of Insoluble Rust Waste for the Synthesis of Iron-Containing Perovskite-Type Catalysts

Insoluble rust waste from the scraping of rusted iron-containing materials represents a cheap, eco-friendly, and available source of iron. LaFeO3 perovskite-type powders were successfully prepared by solution combustion synthesis using rust waste from an electricity transmission tower manufacturer. Solution combustion synthesis enabled introduction of this insoluble iron precursor directly into the final product, bypassing complex extraction procedures. Catalytic activity in the propylene oxidation of the waste-derived LaFeO3 with stoichiometric Fe/La ratio was almost identical to the commercial iron nitrate-derived LaFeO3 , thus demonstrating the viability of this recycling solution. The amount of waste iron precursor was varied and its effect on the powder properties was investigated. A lesser stoichiometric amount of precursor produced a LaFeO3 -La2O3 binary system, whereas a higher stoichiometric amount led to a LaFeO3 -Fe2O3 binary system. Catalytic activity of iron-rich compositions in the propylene oxidation was only slightly lower than the stoichiometric one, whereas iron-poor compositions were much less active. This eco-friendly methodology can be easily extended to other iron perovskites with different chemical compositions and to other iron-containing compounds

Still Worth Fighting Over? A Joint Response

Readers may recall that in the Autumn 2002 issue of the Naval War College Review, Professor James F. Miskel, of the National Security Decision Making Department, argued that the U.S. government often defines national interests in such general terms that its specific goals are not clearly communicated to the American public and to other governments.1 In the Spring 2003 issue, Professor P. H. Liotta, also of the National Security Decision Making Department, responded with a counter- essay arguing that while distinguishing core strategic interests—those for which Americans would be willing to die—from significant interests is almost never easy, it is also essential

Universal decay law in charged-particle emission and exotic cluster radioactivity

A linear universal decay formula is presented starting from the microscopic mechanism of the charged-particle emission. It relates the half-lives of monopole radioactive decays with the $Q$-values of the outgoing particles as well as the masses and charges of the nuclei involved in the decay. This relation is found to be a generalization of the Geiger-Nuttall law in $\alpha$ radioactivity and explains well all known cluster decays. Predictions on the most likely emissions of various clusters are presented.Comment: 2 figure

Fluids Geochemistry of Stromboli

An accurate description of the geochemical system is presented here based on a review of scientific work performed during the past decade. The surface manifestations of the volcanic system of Stromboli have been investigated using several measuring techniques. Studying the chemical composition of the volcanic plume and of fumarolic emissions has provided information on magma degassing processes. The total fluxes of the emitted gases from both the plume and the soil were found to vary with changes in volcanic activity (from normal Strombolian activity to effusive and/or paroxysmal activity). Thermal water results from the interaction between volcanic gases, host rock, seawater and meteoric water and temporal changes observed in the chemical and the isotopic composition of the gases dissolved into thermal waters highlighted the rising of new magma batches. Combining modelling of gas-water-rock interactions with an understanding of the volcanic system allowed to identify preferential sampling sites and parameters for the geochemical monitoring of volcanic activity at Stromboli Island

Strontium and iron-doped barium cobaltite prepared by solution combustion synthesis: exploring a mixed-fuel approach for tailored intermediate temperature solid oxide fuel cell cathode materials

Ba0.5Sr0.5Co0.8Fe0.2O3–δ (BSCF) powders were prepared by solution combustion synthesis using single and double fuels. The effect of the fuel mixture on the main properties of this well-known solid oxide fuel cell cathode material with high oxygen ion and electronic conduction was investigated in detail. Results showed that the fuel mixture significantly affected the area-specific resistance of the BSCF cathode materials, by controlling the oxygen deficiency and stabilizing the Co2+ oxidation state. It was demonstrated that high fuel-to-metal cations molar ratios and high reducing power of the combustion fuel mixture are mainly responsible for the decreasing of the area-specific resistance of BSCF cathode materials. Moreover, a new metastable monoclinic phase with Ba0.5Sr0.5CO3 composition was discovered in the as-burned BSCF powders, enlarging the existing information on the BSCF phase formation mechanis

Molecular structure of highly-excited resonant states in 24^{24}Mg and the corresponding 8^8Be+16^{16}O and 12^{12}C+12^{12}C decays

Exotic $^8$Be and $^{12}$C decays from high-lying resonances in $^{24}$Mg are analyzed in terms of a cluster model. The calculated quantities agree well with the corresponding experimental data. It is found that the calculated decay widths are very sensitive to the angular momentum carried by the outgoing cluster. It is shown that this property makes cluster decay a powerful tool to determine the spin as well as the molecular structures of the resonances.Comment: 17 pages, no figur

First Evidence of Tris(catecholato)silicate Formation from Hydrolysis of an Alkyl Bis(catecholato)silicate

The hydrolysis of 3-ammoniumpropylbis(catecholato)silicate 1, giving two different silica-based materials containing different amounts of tris(catecholato)silicate, is reported. The latter species can be formed through an attack of catechol to the silicon atom in the pentacoordinate complex, in which the silicon-carbon bond is further activated toward electrophilic proton cleavage. The Knoevenagel reaction was used as a probe in order to test the availability of functional groups on the surface of such materials