Local and subquotient inheritance of the heart¶of a Jordan system

We establish the inheritance of the heart by local algebras and subquotients of Jordan and associative systems. Received: 8 May 2001     

Rapid Phase Transitions of Thermotropic Glycolipid Quasicrystal and Frank-Kasper Mesophases: A Mechanistic Rosetta Stone

Experimental results are presented that serve to lower the barrier for developing the science and technology of non-classical thermotropic glycolipid mesophases, which now include dodecagonal quasicrystal (DDQC) and Frank–Kasper (FK) A15 and σ mesophases that can be produced under mild conditions from a versatile class of sugar-polyolefin conjugates. By employing “alloys” comprised of mono- and disaccharide-polyolefin conjugates, and optionally with vitamin E as a small molecule phase modulator, we report the spontaneous formation of stable A15 mesophases at ambient temperature. We further document a rich thermotropic phase map that includes DDQC, A15, and σ mesophases of tunable periodicity that are connected through rapid thermotropic phase transitions as a function of increasing temperature in the order: liquid-like packing (LLP)→DDQC → A15→σ→ disorder. This first direct observation of a rapid thermotropic A15→σ phase transition provides support for a diffusionless martensitic process proceeding through strain-induced introduction of planar defects into the A15 lattice.     

Molecular imprinting-based separation methods for selective analysis of fluoroquinolones in soils

Molecularly imprinted polymers (MIPs) for fluoroquinolone antibiotics (FQs) have been synthesised in one single preparative step by precipitation polymerisation using ciprofloxacin (CIP) as template. Combinations of methacrylic acid (MAA) or 4-vinylpyridine (VP) as functional monomers, ethylene glycol dimethacrylate as crosslinker and dichloromethane, methanol, acetonitrile or toluene as porogens were tested. The experiments carried out by molecularly imprinted solid-phase extraction (MISPE) in cartridges did not allow to detect any imprint effect in the VP-based polymers whereas it was clearly observed in the MAA-based polymers. Among them, the MIP prepared in methanol using MAA as monomer showed the best performance and was chosen for further experiments. The ability of the selected MIP for the selective recognition of other widely used FQs (enoxacin, norfloxacin, danofloxacin and enrofloxacin) and quinolones (Qs) (cinoxacin, flumequine, nalidixic acid and oxolinic acid) was evaluated. The obtained results revealed the high selectivity of the obtained polymer, which was able to distinguish between FQs, that were recognised and retained onto the MIP cartridge, and Qs, which were washed out during loading and washing steps. The MIP was then packed into a stainless steel column (50mmx4.6mm i.d.) and evaluated as chromatography column for screening of FQs in soil samples. The mobile phase composition, flow rate, and the elution profile were then optimised in order to improve peak shape without sacrifying imprinting factor. Finally, under optimised conditions, soil samples spiked with CIP or with a mixture of fluoroquinolones in concentration of 0.5microgg(-1) were successfully analysed by the developed MIP-based procedures.     

Kinetic study of the nitric oxide oxidation between 288 and 323 K,under pressure,focus on the oxygen influence on the reaction rate constant

The sequestration of carbon dioxide fumes from oxyfuel combustion is used to reduce significantly the carbon dioxide emissions from coal-fired power plants. Impurities like nitric oxide, present in the fumes, can cause technical difficulties during the capture, the treatment, the transport, and the storage steps of the CO₂ fumes. The purpose of this study is to better understand the oxidation of nitric oxide under pressure in the presence of carbon dioxide and in the experimental condition of flue gas treatment. This reaction is known to be a third-order reaction, two order in nitric oxide and first order in oxygen. To examine the effect of the temperature, the pressure and the volume fraction of oxygen on the rate constant of oxidation, k₁, an autoclave is used. The first experiment studies the influence of the temperature between 288 and 323 K. The results found are in the form of an Arrhenius-type equation: k₁ = 810 exp^(620/T) and are in agreement with the literature. Carbon dioxide does not seem to have an influence on the rate constant, whereas our experimental measurements indicate an influence of the volume fraction of oxygen. The rate constant decreases when the oxygen volume fraction increases by up to 10%. Then the rate constant remains constant. This observation allows us to conclude that the mechanism involving the mechanism with a dimer of NO as an intermediate is more likely to be the mechanism involved in the nitric oxide oxidation in our experimental conditions: high pressure and ambient temperature. The rate constant k₂, k_–2, and k₃ were also estimated in these conditions.     

Surface modified‐magnetic nanoparticles by molecular imprinting for the dispersive solid‐phase extraction of triazines from environmental waters

Magnetic nanoparticles have been surface modified by molecular imprinting and evaluated as selective sorbents for the extraction of triazines from environmental waters. The use of propazine as template allowed us to synthesize a selective material able to simultaneously recognize and selective extract not only the template but also several other herbicides of the same family. A magnetic molecularly imprinted‐based dispersive solid‐phase extraction procedure was developed and fully optimized. Magnetic molecularly imprinted polymer particles can be easily collected and separated from liquid solvents and samples with the help of an external magnetic field, avoiding in that way any centrifugation or filtration steps, which represents a remarkable advantage over traditional procedures. Under optimum conditions, selective extraction of several triazines (cyanazine, simazine, atrazine, propazine, and terbutylazine) from environmental water samples was performed prior to final determination by high‐performance liquid chromatography with diode‐array detection. Recoveries for the studied triazines were within the range of 75.2–94.1%, with relative standard deviations lower than 11.3% (n = 3). The limits of detection were within 0.16–0.51 µg/L, depending upon the triazine and the type of sample analyzed.     

Parisian Ruin with Erlang Delay and a Lower Bankruptcy Barrier

Methodology and Computing in Applied Probability - Parisian ruin occurs once the surplus stays continuously below zero for a given period. We consider the spectrally negative Lévy risk process...     

A scintillator-based particle detector for CRYRING@ESR

With the unprecedented range of ion species and energies offered by the newly commissioned CRYRING facility, the availability of single ion detectors is of significant importance as part of standard instrumentation as well as for novel experiments. A detector system was constructed on the basis of the YAP:Ce crystal scintillator, which is at once radiation-hard, fast, and affordable. Results of a characterization experiment confirmed the feasibility of the setup for incident ion rates on the order of MHz and found a critical fluence of some 10¹³ cm⁻² upon which the crystal is rendered locally blind to further ion irradiation. The device was first used in CRYRING commissioning runs in August and November 2018. Future efforts will complete the integration of the detector into the GSI control and data acquisition system MBS.     

Regio- and stereocontrol in the alternating copolymerization of olefins with carbon monoxide

Strictly alternating copolymers between olefins and carbon monoxide are synthesized using cationic palladium catalysts modified by phosphorus or nitrogen ligands. Basic chelate diphosphines as the ligand allow the regioregular copolymerization of aliphatic olefins thus affording, e.g. in the case of propene, poly(1-oxo-2-methyltrimethylene). Steric control of the copolymerization process towards the production of overwhelmingly isotactic copolymers is possible particularly when using atropisomeric ligands. In the case of styrene as the substrate and for all ligands employed the copolymerization process is regioregular. Prevailing syndiotactic structure is obtained with 1,10-phenanthroline or 2,2′-bipyridine as the ligand. Chelate thioether ligands allow the preparation of a completely atactic material. For 4-tert-butylstyrene an isotactic structure became accessible by using chiral bisoxazolidines. The prevailing structure of the copolymers of cyclopentene corresponds to a 1,3-enchainment of the olefin units most probably associated with a prevailing diisotactic structure