Mixed bi-material electrodes based on LiMn2O4 and activated carbon for hybrid electrochemical energy storage devices

The performance of mixed bi-material electrodes composed of the battery material, LiMn₂O₄, and the electrochemical capacitor material, activated carbon, for hybrid electrochemical energy storage devices is investigated by galvanostatic charge/discharge and pulsed discharge experiments. Both, a high and a low conductivity lithium-containing electrolyte are used. The specific charge of the bi-material electrode is the linear combination of the specific charges of LiMn₂O₄ and activated carbon according to the electrode composition at low discharge rates. Thus, the specific charge of the bi-material electrode falls between the specific charge of the activated carbon electrode and the LiMn₂O₄ battery electrode. The bi-material electrodes have better rate capability than the LiMn₂O₄ battery electrode. For high current pulsed applications the bi-material electrodes typically outperform both the battery and the capacitor electrode.     

Ruthenium- and Osmium-Arene Complexes of 2-Substituted Indolo[3,2-c]quinolines: Synthesis, Structure, Spectroscopic Properties, and Antiproliferative Activity

The synthesis of new modified indolo[3,2-c]quinoline ligands L(1)-L(8) with metal-binding sites is reported. By coordination to ruthenium- and osmium-arene moieties 16 complexes of the type [(η(6)-p-cymene)M(L)Cl]Cl (1a,b-8a,b), where M is Ru(II) or Os(II) and L is L(1)-L(8), have been prepared. All compounds were comprehensively characterized by elemental analysis, electrospray ionization mass spectrometry, IR, UV-vis, and NMR spectroscopy, thermogravimetric analysis, and single-crystal X-ray diffraction (2a, 4a, 4b, 5a, 7a, and 7b). The complexes were tested for antiproliferative activity in vitro in three human cancer cell lines, namely, CH1 (ovarian carcinoma), SW480 (colon adenocarcinoma), and A549 (non-small-cell lung cancer), yielding IC(50) values in the submicromolar or low micromolar range.     

Nanoparticle Transport in Epithelial Cells: Pathway Switching Through Bioconjugation

The understanding and control of nanoparticle transport into and through cellular compartments is central to biomedical applications of nanotechnology. Here, it is shown that the transport pathway of 50 nm polystyrene nanoparticles decorated with vitamin B₁₂ in epithelial cells is different compared to both soluble B₁₂ ligand and unmodified nanoparticles, and this is not attributable to B₁₂ recognition alone. Importantly, the study indicates that vitamin B₁₂‐conjugated nanoparticles circumnavigate the lysosomal compartment, the destination of soluble vitamin B₁₂ ligand. Whereas cellular trafficking of soluble B₁₂ is confirmed to occur via the clathrin‐mediated pathway, transport of B₁₂‐conjugated nanoparticles appears to predominantly take place by a route that is perturbed by caveolae‐specific inhibitors. This data suggests that, following its conjugation to nanoparticles, in addition to dramatically increasing the cellular uptake of nanoparticles, the normal cell trafficking of B₁₂ is switched to an alternative pathway, omitting the lysosomal stage: a result with important implications for oral delivery of nanoparticulate diagnostics and therapeutics.     

Photocatalytic properties of TiO2 supported on SBA-15 mesoporous materials with large pores and short channels

In this study, the new class of SBA-15 mesoporous materials with large pore diameter and short pore channels has been utilized as template for TiO₂ based photocatalysts. The samples were characterized by TEM, SAXS, and BET and tested for photocatalytic activity in liquid phase oxidation of phenol. This is the first ever application of this type of SBA-15 supported catalyst in photocatalytic area. This work also included the novel use of sub-1 nm Au nanoparticles for catalysts modification which doubles the phenol oxidation rate.     

Impact of Particle Generation Method on the Apparent Hygroscopicity of Insoluble Mineral Particles

Calcite (CaCO ₃ ) mineral particles are commonly generated by atomization techniques to study their heterogeneous chemistry, hygroscopicity, and cloud nucleation properties. Here we investigate the significant artifact introduced in generating calcium mineral particles through the atomization of a saturated suspension of the powder in water, by measuring particle hygroscopicity via CCN activation curves. Particles produced from atomization displayed hygroscopicities as large as κ_app > 0.1, 100 times more hygroscopic than that obtained for dry-generated calcite, κ_app = 0.0011. The hygroscopicity of the wet-generated particles increased as a function of time the calcite powder spent in water, and with decreasing particle size. Wet-generated calcium oxalate was more hygroscopic through wet- (κ_app = 0.34) versus dry-generation (κ_app = 0.048). Atomized calcium sulfate particles, however, were only slightly more hygroscopic (κ_app = 0.0045) than those generated dry (κ_app = 0.0016). Single-particle analysis by ATOFMS and SEM/EDX, and bulk analysis of the calcite powders by ICP-MS and IC revealed no significant soluble contaminants. The atomized particles were likely composed of components that dissolved from the powder and then re-precipitated, and appeared to contain little of the original mineral powder. The increased hygroscopicity of atomized calcite may have been caused by aqueous carbonate chemistry producing Ca(OH) ₂ , Ca(HCO ₃ ) ₂ , and metastable hydrates with increased solubility. Surface water adsorption may have also played a role, in addition to uncharacterized soluble components produced by wet-generation, and the precipitation of amorphous phases including glassy states. This study suggests that using wet-generation methods to suspend mineral dust samples will not produce particles with the correct physicochemical properties in laboratory studies, a finding which has important implications for past and future laboratory studies focusing on understanding relationships between the hygroscopicity and chemistry of mineral dust particles.     

QUANTITATIVE GAS CHROMATOGRAPHIC ANALYSIS OF AMINO ACIDS IN BEER AND WORT

Amino acids present in beer and wort samples were isolated using Dowex 50W-X8 ion exchange resin. These acids were converted to N-trifluoroacetyl methyl esters and were separated on a 10 ft. x 1/4 in. copper column packed with 3/4% Carbowax 1540 and 1/4% NPGS on Chromosorb W. Complete separation and quantitative estimation was obtained for eleven amino acids: valine, alanine, isoleucine, leucine, glycine, proline, aspartic acid, threonine, methionine, glutamic acid, and phenylalanine. Standards of the acids showed a relative standard deviation of 4% and less for nine acids while threonine and methionine gave deviations of 9% and 15% respectively. The other naturally-occurring amino acids did not interfere with the separation of the above eleven. Amino acid assimilation data is presented along with other beer and wort analyses.     

Influence of the geometry on the pressure distribution of granular heaps

We investigate the effect of the geometry of granular heaps on the pressure distribution. For given pressure distributions under cones we compute the pressure distribution under wedges using linear superposition. For cones with a pressure minimum, the pressure minimum for the corresponding wedge vanishes. Comparisons with experimental data gives good qualitative aggreement, but the total pressure is overestimated.     

Inference of monotonicity constraints in Datalog programs

Datalog (i.e., function-free logic) programs with monotonicity constraints on extensional predicates are considered. A monotonicity constraint states that one argument of a predicate or a constant is always less than another argument or a constant, according to some strict partial order. Relations of an extensional database are required to satisfy the monotonicity constraints imposed on their predicates. More specifically, a strict partial order is defined on the domain (i.e., set of constants) of the database, and every tuple of each relation satisfies the monotonicity constraints imposed on its predicate. This paper focuses on the problem of entailment of monotonicity constraints in the intensional database from monotonicity constraints in the extensional database. The entailment problem is proven to be decidable, based on a suggested algorithm for computing sound and complete disjunctions of monotonicity and equality constraints that hold in the intentional database. It is also shown that the entailment of monotonicity constraints in programs is a complete problem for exponential time. For linear programs, this problem is complete for polynomial space. This revised version was published online in June 2006 with corrections to the Cover Date.     

Calcination of limestone in a tubular reactor

Theoretical expressions were developed for the design of a tubular reactor for the calcination of limestone, pneumatically conveyed by flue gas. The total residence time and the length of the reactor are affected in particular by the particle size, the excess thermal capacity of the gas and the heat transfer coefficient. High throughput can be achieved in relatively small reactors. An experimental investigation verified a theoretical prediction, that a considerable part of the decomposition takes place in the first few centimeters of the reactor length. The rate of heat transfer in this section was high, with Nusselt numbers of 9.9 to 31.7.