434 research outputs found
Thermodynamics of the two-dimensional Falicov-Kimball model: a classical Monte Carlo study
The two-dimensional Falicov-Kimball (FK) model is analyzed using Monte Carlo
method. In the case of concentrations of both itinerant and localized particles
equal to 0.5 we determine temperature dependence of specific heat, charge
density wave susceptibility and density-density correlation function. In the
weak interaction regime we find a first order transition to the ordered state
and anomalous temperature dependence of the correlation function. We construct
the phase diagram of half-filled FK model. Also, the role of
next-nearest-neighbor hopping on the phase diagram is analyzed. Lastly, we
discuss the density of states and the spectral functions for the mobile
particles in weak and strong interaction regime.Comment: 15 pages, RevTe
The new features of landslide relief discovered using LiDAR – case study from Babia Góra massif, Western Carpathian Mountains
Basing on LiDAR data, the re-interpretation of the limit and distribution of the selected landslide forms in 9 test areas were carried out. The forms are located at the slopes of the monoclinal ridge of Babia Góra Mt. (1,725 m a.s.l.) in the flysch Western Carpathians. The earlier knowledge on these landforms is shown in the unpublished map at the scale of 1:5,000 which was prepared basing on geomorphological mapping. Basing on the newest information source, subtle geomorphic signatures of landslides were found, the dynamics of these forms and directions of their further development were determined. Local differentiation of deep-seated landslides was indicated according to the relation between the sandstone layer dip and slope inclination, slope length, and altitude of the location of headwaters. An attention was paid to polycyclic relief of the highest located landslide forms, which contain the elements of glacial and nival morphology, and some are modelled by debris flows
Hofstadter butterfly for a finite correlated system
We investigate a finite two-dimensional system in the presence of external
magnetic field. We discuss how the energy spectrum depends on the system size,
boundary conditions and Coulomb repulsion. On one hand, using these results we
present the field dependence of the transport properties of a nanosystem. In
particular, we demonstrate that these properties depend on whether the system
consists of even or odd number of sites. On the other hand, on the basis of
exact results obtained for a finite system we investigate whether the
Hofstadter butterfly is robust against strong electronic correlations. We show
that for sufficiently strong Coulomb repulsion the Hubbard gap decreases when
the magnetic field increases.Comment: 7 pages, 5 figures, revte
Completing the triad: Synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Oxidation of M(CO) (M = Cr, Mo, W) with the synergistic oxidative system Ag[WCA]/0.5 I yields the fully characterized metalloradical salts [M(CO)]+˙[WCA]− (weakly coordinating anion WCA = [F-{Al(OR)}], R = C(CF)). The new metalloradical cations with M = Mo and W showcase a similar structural fluxionality as the previously reported [Cr(CO)]˙. Their reactivity increases from M = Cr < Mo < W and their syntheses allow for in-depth insights into the properties of the group 6 carbonyl triad. Furthermore, the reaction of NO[WCA] with neutral carbonyl complexes M(CO) gives access to the heteroleptic carbonyl/nitrosyl cations [M(CO)(NO)] as salts of the WCA [Al(ORF)], the first complete transition metal triad of their kind
Mechanisms of immune modulation in the tumor microenvironment and implications for targeted therapy
Cancer; Immunosuppression mechanisms; Tumor microenvironmentCáncer; Mecanismos de inmunosupresión; Microambiente tumoralCàncer; Mecanismes d'immunosupressió; Microambient tumoralThe efficacy of cancer therapies is limited to a great extent by immunosuppressive mechanisms within the tumor microenvironment (TME). Numerous immune escape mechanisms have been identified. These include not only processes associated with tumor, immune or stromal cells, but also humoral, metabolic, genetic and epigenetic factors within the TME. The identification of immune escape mechanisms has enabled the development of small molecules, nanomedicines, immune checkpoint inhibitors, adoptive cell and epigenetic therapies that can reprogram the TME and shift the host immune response towards promoting an antitumor effect. These approaches have translated into series of breakthroughs in cancer therapies, some of which have already been implemented in clinical practice. In the present article the authors provide an overview of some of the most important mechanisms of immunosuppression within the TME and the implications for targeted therapies against different cancers
Analysis of Yarrowia lipolytica Growth, Catabolism, and Terpenoid Biosynthesis during Utilization of Lipid-derived Feedstock
This study employs biomass growth analyses and 13C-isotope tracing to investigate lipid feedstock utilization by Yarrowia lipolytica. Compared to glucose, oil-feedstock in the minimal medium increases the yeast\u27s biomass yields and cell sizes, but decreases its protein content (\u3c20% of total biomass) and enzyme abundances for product synthesis. Labeling results indicate a segregated metabolic network (the glycolysis vs. the TCA cycle) during co-catabolism of sugars (glucose or glycerol) with fatty acid substrates, which facilitates resource allocations for biosynthesis without catabolite repressions. This study has also examined the performance of a β-carotene producing strain in different growth mediums. Canola oil-containing yeast-peptone (YP) has resulted in the best β-carotene titer (121 ± 13 mg/L), two-fold higher than the glucose based YP medium. These results highlight the potential of Y. lipolytica for the valorization of waste-derived lipid feedstock
In Situ Small-Angle X-ray Scattering Studies During Reversible Addition–Fragmentation Chain Transfer Aqueous Emulsion Polymerization
Polymerization-induced self-assembly (PISA) is a powerful platform technology for the rational and efficient synthesis of a wide range of block copolymer nano-objects (e.g., spheres, worms or vesicles) in various media. In situ small-angle X-ray scattering (SAXS) studies of reversible addition–fragmentation chain transfer (RAFT) dispersion polymerization have previously provided detailed structural information during self-assembly (see M. J. Derry et al., Chem. Sci. 2016, 7, 5078–5090). However, conducting the analogous in situ SAXS studies during RAFT aqueous emulsion polymerizations poses a formidable technical challenge because the inherently heterogeneous nature of such PISA formulations requires efficient stirring to generate sufficiently small monomer droplets. In the present study, the RAFT aqueous emulsion polymerization of 2-methoxyethyl methacrylate (MOEMA) has been explored for the first time. Chain extension of a relatively short non-ionic poly(glycerol monomethacrylate) (PGMA) precursor block leads to the formation of sterically-stabilized PGMA-PMOEMA spheres, worms or vesicles, depending on the precise reaction conditions. Construction of a suitable phase diagram enables each of these three morphologies to be reproducibly targeted at copolymer concentrations ranging from 10 to 30% w/w solids. High MOEMA conversions are achieved within 2 h at 70 °C, which makes this new PISA formulation well-suited for in situ SAXS studies using a new reaction cell. This bespoke cell enables efficient stirring and hence allows in situ monitoring during RAFT emulsion polymerization for the first time. For example, the onset of micellization and subsequent evolution in particle size can be studied when preparing PGMA29-PMOEMA30 spheres at 10% w/w solids. When targeting PGMA29-PMOEMA70 vesicles under the same conditions, both the micellar nucleation event and the subsequent evolution in the diblock copolymer morphology from spheres to worms to vesicles are observed. These new insights significantly enhance our understanding of the PISA mechanism during RAFT aqueous emulsion polymerization
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