62 research outputs found

    Communication satellite technology trends

    Get PDF
    A chronology of space-Earth interconnectivity is presented. The Advanced Communications Technology Satellite (ACTS) system, Land Mobile Satellite, space-Earth antennas, impact of antenna size on coverage, intersatellite links are outlined. This presentation is represented by graphs and charts only

    Rapid, room-temperature, solvent-free mechanochemical oxidation of elemental gold into organosoluble gold salts

    Get PDF
    Gold is highly valued for a wide range of commercial and technological applications but is processed exclusively through highly aggressive and toxic solvents and/or reagents, ultimately yielding water-soluble salts that are difficult to separate from inorganic reaction byproducts. As a result, development of safer, cleaner processes that would enable gold processing in non-aqueous, organic solvent is an attractive technological goal. Here, we describe a methodology that simultaneously avoids aggressive reagents and enables gold extraction into a safe organic solvent. The methodology is based on solventless, mechanochemical oxidation of metallic gold with Oxone® in the presence of tetraalkylammonium halide salts, to directly, rapidly (within 30–60 minutes) and at room temperature convert gold metal into solid salts that are immediately soluble in pure organic solvents and aqueous alcoholic media. The organosoluble gold salts are easily separated from sulfate byproducts by direct extraction into the benign solvent ethyl acetate, which is also easily recycled for re-use, providing a strategy for gold activation and dissolution without any additional reagents for purification, such as cation exchange resins, salts, or chelating agents. Besides enabling direct extraction of gold into an organic solvent, the mechanochemically obtained organosoluble gold salts can also be readily used for further syntheses, as shown here by a two-step one-pot route to prepare air- and moisture-resistant Au(i) salts, and an improved synthesis of gold nanoparticles from bulk gold

    Biophysical properties of dimeric phospholipids

    No full text
    A series of unusual bipolar and bis-phospholipids (dimeric phospholipids) have been studied. The structure, conformation, morphology and biophysical properties of the resulting phospholipid aggregates were investigated.Deuterium magnetic resonance spectroscopy (sp2 sp2H NMR) was used to study and characterize the conformation and acyl chain order in oriented bipolar lipid membranes. The sp2 sp2H-NMR studies indicated a large and constant value for the order parameter (Srmsbmol) rm sb{mol}) for all positions along the bipolar lipid diacyl chain for mechanically oriented, magnetically oriented and unoriented samples. This indicates that the great majority (>>90%) of the bipolar lipid exists in a highly ordered spanning conformation.Dimeric phospholipid aggregate morphologies were studied using sp31 sp{31}P NMR, small angle X-ray scattering, electron microscopy, differential scanning calorimetry, and the Langmuir film balance technique in order to study the relationship between lipid structure and aggregate morphology. Dimeric phospholipids favour a lamellar morphology. A number of lipid structure-dependent features have been observed including tri-lamellar structures, extended ripple phases and hexagonal phases.Dimeric and non-hydrolyzable phospholipids were used to study the phenomenon of interfacial activation of extracellular phospholipase Asb2 sb2 (EC. 3.1.1.4) (PLAsb2) sb2) in relation to lipid phase, substrate conformation and mobility. Kinetic results and product analyses are consistent with a situation where the spanning conformer of bipolar phospholipids is resistant to PLAsb2 sb2-catalyzed hydrolysis but the hairpin conformer is readily hydrolyzed. Finally, an analysis of interfacial kinetics in non-hydrolyzable matrices indicated varying degrees of interfacial inhibition and hydrolysis product activation. This has not been explicitly recognized before and affects the choice of assay conditions for PLA$ sb2.

    Imaging the Selective Binding of Synapsin to Anionic Membrane Domains

    No full text
    Synapsins are membrane-associated proteins that cover the surface of synaptic vesicles and are responsible for maintaining a pool of neurotransmitter-loaded vesicles for use during neuronal activity. We have used atomic force microscopy (AFM) to study the interaction of synapsin I with negatively charged lipid domains in phase-separated supported lipid bilayers prepared from mixtures of phosphatidylcholines (PCs) and phosphatidylserines (PSs). The results indicate a mixture of electrostatic binding to anionic PS-rich domains as well as some nonspecific binding to the PC phase. Interestingly, both protein binding and scanning with synapsin-coated AFM tips can be used to visualize charged lipid domains that cannot be detected by topography alone.NRC publication: Ye
    corecore