Separation of n-hexane - ethyl acetate mixture by azeotropic batch distillation with heterogeneous entrainers

In this article, a systematic study of the separation of the n-hexane - ethyl acetate mixture with an entrainer by heterogeneous azeotropic batch distillation is performed. Based upon the thermodynamic behaviour of the ternary mixtures, potential entrainers partially miscible with one or two original azeotropic components are chosen. In all cases, the entrainer adds a heterogeneous binary or ternary azeotrope that is the lowest boiling point in the ternary diagram. Therefore, it leaves the column by the overhead stream which is subcooled to get two liquid phases in the decanter. The phase with the highest amount of the original component is removed as distillate product whereas the entrainer – rich phase is continuously refluxed to the column. Considering methanol, acetonitrile, water and nitromethane as heterogeneous entrainers, screening was performed based on the composition of the unstable heteroazeotropic mixture, the ratio of both liquid phases in the condensed top vapour and the purity of the distillate product determined by the liquid – liquid envelope at the decanter temperature. The process feasibility analysis is validated by using rigorous simulation with the batch process simulator ProSimBatch. Simulation results are then corroborated in a bench experimental column for the selected entrainer, showing several advantages of heterogeneous batch distillation compared to homogeneous systems

Tangent fermions: Dirac or Majorana fermions on a lattice without fermion doubling

I. Introduction II. Two-dimensional lattice fermions III. Methods to avoid fermion doubling (sine dispersion, sine plus cosine dispersion, staggered lattice dispersion, linear sawtooth dispersion, tangent dispersion) IV. Topologically protected Dirac cone V. Application: Klein tunneling (tangent fermions on a space-time lattice, wave packet propagation) VI. Application: Strong antilocalization (transfer matrix of tangent fermions, topological insulator versus graphene) VII. Application: Anomalous quantum Hall effect (gauge invariant tangent fermions, topologically protected zeroth Landau level) VIII. Application: Majorana metal (Dirac versus Majorana fermions, phase diagram) IX. OutlookComment: review article, 26 pages, 13 figures; V2: added three appendices, and provided code for the various implementation

Dynamical simulation of the injection of vortices into a Majorana edge mode

The chiral edge modes of a topological superconductor can transport fermionic quasiparticles, with Abelian exchange statistics, but they can also transport non-Abelian anyons: Majorana zero-modes bound to a {\pi}-phase domain wall that propagates along the boundary. Such an edge vortex is injected by the application of an h/2e flux bias over a Josephson junction. Existing descriptions of the injection process rely on the instantaneous scattering approximation of the adiabatic regime, where the internal dynamics of the Josephson junction is ignored. Here we go beyond that approximation in a time-dependent many-body simulation of the injection process, followed by a braiding of the mobile edge vortex with an immobile Abrikosov vortex in the bulk of the superconductor. Our simulation sheds light on the properties of the Josephson junction needed for a successful implementation of a flying Majorana qubit.Comment: 13 pages 12 figure

Factors controlling interannual variability of vertical organic matter export and phytoplankton bloom dynamics – a numerical case-study for the NW Mediterranean Sea

Mid-latitude spring blooms of phytoplankton show considerable year-to-year variability in timing, spatial extent and intensity. It is still unclear to what degree the bloom variability is connected to the magnitude of the vertical flux of organic matter. A coupled three-dimensional hydrodynamic-biogeochemical model is used to relate interannual variability in phytoplankton spring-bloom dynamics to variability in the vertical export of organic matter in the NW Mediterranean Sea. Simulation results from 2001 to 2010, validated against remote-sensing chlorophyll, show marked interannual variability in both timing and shape of the bloom. Model results show a tendency for the bloom to start later after cold and windy winters. However, the onset of the bloom occurs often when the mixed layer is still several hundred metres deep while the heat flux is already approaching zero and turbulent mixing is low. Frequency and intensity of wind episodes control both the timing and development of the bloom and the consequent export flux of organic matter. The wintertime flux is greater than zero and shows relatively low interannual variability. The magnitude of the interannual variability is mainly determined in March when the frequency of windy days positively correlates with the export flux. Frequent wind-driven mixing episodes act to increase the export flux and, at the same time, to interrupt the bloom. Perhaps counterintuitively, our analysis shows that years with discontinuous, low-chlorophyll blooms are likely to have higher export flux than years with intense uninterrupted blooms. The NW Mediterranean shows strong analogy with the North Atlantic section within the same latitude range. Hence, our results may also be applicable to this quantitatively more important area of the world ocean

Structures of Receptor Complexes of a North American H7N2 Influenza Hemagglutinin with a Loop Deletion in the Receptor Binding Site

Human infections with subtype H7 avian influenza viruses have been reported as early as 1979. In 1996, a genetically stable 24-nucleotide deletion emerged in North American H7 influenza virus hemagglutinins, resulting in an eight amino acid deletion in the receptor-binding site. The continuous circulation of these viruses in live bird markets, as well as its documented ability to infect humans, raises the question of how these viruses achieve structural stability and functionality. Here we report a detailed molecular analysis of the receptor binding site of the North American lineage subtype H7N2 virus A/New York/107/2003 (NY107), including complexes with an avian receptor analog (3′-sialyl-N-acetyllactosamine, 3′SLN) and two human receptor analogs (6′-sialyl-N-acetyllactosamine, 6′SLN; sialyllacto-N-tetraose b, LSTb). Structural results suggest a novel mechanism by which residues Arg220 and Arg229 (H3 numbering) are used to compensate for the deletion of the 220-loop and form interactions with the receptor analogs. Glycan microarray results reveal that NY107 maintains an avian-type (α2-3) receptor binding profile, with only moderate binding to human-type (α2-6) receptor. Thus despite its dramatically altered receptor binding site, this HA maintains functionality and confirms a need for continued influenza virus surveillance of avian and other animal reservoirs to define their zoonotic potential

Mifepristone increases mRNA translation rate, triggers the unfolded protein response, increases autophagic flux, and kills ovarian cancer cells in combination with proteasome or lysosome inhibitors

The synthetic steroid mifepristone blocks the growth of ovarian cancer cells, yet the mechanism driving such effect is not entirely understood. Unbiased genomic and proteomic screenings using ovarian cancer cell lines of different genetic backgrounds and sensitivities to platinum led to the identification of two key genes upregulated by mifepristone and involved in the unfolded protein response (UPR): the master chaperone of the endoplasmic reticulum (ER), glucose regulated protein (GRP) of 78 kDa, and the CCAAT/enhancer binding protein homologous transcription factor (CHOP). GRP78 and CHOP were upregulated by mifepristone in ovarian cancer cells regardless of p53 status and platinum sensitivity. Further studies revealed that the three UPR-associated pathways, PERK, IRE1α, and ATF6, were activated by mifepristone. Also, the synthetic steroid acutely increased mRNA translation rate, which, if prevented, abrogated the splicing of XBP1 mRNA, a non-translatable readout of IRE1α activation. Moreover, mifepristone increased LC3-II levels due to increased autophagic flux. When the autophagic–lysosomal pathway was inhibited with chloroquine, mifepristone was lethal to the cells. Lastly, doses of proteasome inhibitors that are inadequate to block the activity of the proteasomes, caused cell death when combined with mifepristone; this phenotype was accompanied by accumulation of poly-ubiquitinated proteins denoting proteasome inhibition. The stimulation by mifepristone of ER stress and autophagic flux offers a therapeutic opportunity for utilizing this compound to sensitize ovarian cancer cells to proteasome or lysosome inhibitors.Fil: Zhang, Lei. University Of South Dakota; Estados UnidosFil: Hapon, María Belén. University Of South Dakota; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; ArgentinaFil: Goyeneche, Alicia A.. University Of South Dakota; Estados Unidos. McGill University; CanadáFil: Srinivasan, Rekha. University Of South Dakota; Estados UnidosFil: Gamarra Luques, Carlos Diego. University Of South Dakota; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; ArgentinaFil: Callegari, Eduardo A.. University Of South Dakota; Estados UnidosFil: Drappeau, Donis D.. University Of South Dakota; Estados UnidosFil: Terpstra, Erin J.. University Of South Dakota; Estados UnidosFil: Pan, Bo. University Of South Dakota; Estados UnidosFil: Knapp, Jennifer R.. University of Kansas; Estados UnidosFil: Chien, Jeremy. University of Kansas; Estados UnidosFil: Wang, Xuejun. University Of South Dakota; Estados UnidosFil: Eyster, Kathleen M.. University Of South Dakota; Estados UnidosFil: Telleria, Carlos Marcelo. University Of South Dakota; Estados Unidos. McGill University; Canadá. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentin

A strategy for the characterization of minute chromosome rearrangements using multiple color fluorescence in situ hybridization with chromosome-specific DNA libraries and YAC clones

The identification of marker chromosomes in clinical and tumor cytogenetics by chromosome banding analysis can create problems. In this study, we present a strategy to define minute chromosomal rearrangements by multicolor fluorescence in situ hybridization (FISH) with whole chromosome painting probes derived from chromosome-specific DNA libraries and Alu-polymerase chain reaction (PCR) products of various region-specific yeast artificial chromosome (YAC) clones. To demonstrate the usefulness of this strategy for the characterization of chromosome rearrangements unidentifiable by banding techniques, an 8p+ marker chromosome with two extra bands present in the karyotype of a child with multiple anomalies, malformations, and severe mental retardation was investigated. A series of seven-color FISH experiments with sets of fluorochrome-labeled DNA library probes from flow-sorted chromosomes demonstrated that the additional segment on 8p+ was derived from chromosome 6. For a more detailed characterization of the marker chromosome, three-color FISH experiments with library probes specific to chromosomes 6 and 8 were performed in combination with newly established telomeric and subtelomeric YAC clones from 6q25, 6p23, and 8p23. These experiments demonstrated a trisomy 6pter6p22 and a monosomy 8pter8p23 in the patient. The present limitations for a broad application of this strategy and its possible improvements are discusse