An inflationary bianchi V model with shear and rotation

A Bianchi V model, in the presence of a fluid with shear and rotation, is investigated. Asymptotic solutions are worked out, showing that shear and rotation may give rise to a conflict with present day observations, a problem that can be solved with the help of an inflationary solution.     

Stochastic processes and the non-perturbative structure of the QCD vacuum

Based on a local Gaussian evaluation of the functional integral representation, a method is developed to obtain ground state functionals. The method is applied to the gluon sector of QCD. For the leading term in the ground state functional, stochastic techniques are used to check consistency of the quantum theory, finiteness of the mass gap and the scaling relation in the continuum limit. The functional also implies strong chromomagnetic fluctuations which constrain the propagators in the fermion sector.     

Hydrogen and deuterium trapping at nitrogen in tantalum studied by PAC

PAC experiments using¹⁸¹Hf as probe atom were performed in Ta samples containing 1.1 at% of N and loaded with 0.2 at% of H or of 1.6 at% of D. At room temperature only the known frequency due to N is present. Below 100K or 140K, for H and D respectively, the amplitude of this interaction decreases and two new interaction frequencies characterized by V₀=240MHz, η=0.80 and V₀=250 MHz, η=0.40 appear. These frequencies are attributed to H(D) trapped by N in the vicinity of the probe atom¹⁸¹Hf. The disappearance of these interactions at 100K and 140K is interpreted as a release of H (D) from Hf but not from N. From the data the jump rates of H(D) around N in Ta are derived.     

Selective glycoprotein detection through covalent templating and allosteric click-imprinting

Many glycoproteins are intimately linked to the onset and progression of numerous heritable or acquired diseases of humans, including cancer. Indeed the recognition of specific glycoproteins remains a significant challenge in analytical method and diagnostic development. Herein, a hierarchical bottom-up route exploiting reversible covalent interactions with boronic acids and so-called click chemistry for the fabrication of glycoprotein selective surfaces that surmount current antibody constraints is described. The self-assembled and imprinted surfaces, containing specific glycoprotein molecular recognition nanocavities, confer high binding affinities, nanomolar sensitivity, exceptional glycoprotein specificity and selectivity with as high as 30 fold selectivity for prostate specific antigen (PSA) over other glycoproteins. This synthetic, robust and highly selective recognition platform can be used in complex biological media and be recycled multiple times with no performance decrement.     

Inelastic constitutive equations for complex flows

A new class of inelastic constitutive equations is presented and discussed. In addition to the rate-of-strain tensor, the stress is assumed to depend also on the relative-rate-of-rotation tensor, a frame-indifferent quantity that brings information about the nature of the flow. The material functions predicted by these constitutive equations are given for simple shear and uniaxial extension. A special case of these equations takes the Newtonian form, except that the viscosity is a function of the invariants of both kinematic tensors on which the stress depends. This simple constitutive equation has potential applications in liquid flow process simulations, since it combines simplicity with the capability of responding independently to shear and extension, as real liquids seem to do. Finally, possible forms for the new viscosity function are discussed.     

Temperature dependent Raman scattering study of l-ascorbic acid

Temperature dependent Raman study of l-ascorbic acid has been performed from 15 to 418 K. Changes in the wavenumber vs. temperature plots for some internal modes were interpreted as conformational molecular change and the discontinuity in the wavenumber vs. temperature plots along with the appearance of a new vibrational mode in the temperature range 200-270 K suggests that l-ascorbic acid undergoes a structural phase transition. For temperatures higher than 300 K, no relevant modification was observed on the Raman spectra thus indicating a stable structure at high temperatures. Additionally, a correlation between OH stretching wavenumber and the behavior of hydrogen bond is also made.     

In vitro anti-HMPV activity of meroditerpenoids from marine alga Stypopodium zonale (Dictyotales)

In this paper, we evaluated the antiviral activity against HMPV replication of crude extract of the marine algae Stypopodium zonale and of two meroditerpenoids obtained from it, atomaric acid and epitaondiol, and a methyl ester derivative of atomaric acid. Their selectivity indexes were 20.78, >56.81, 49.26 and 12.82, respectively. Compared to ribavirin, the substances showed a relatively low cytotoxicity on LLC-MK2 cells, with a significant antiviral activity, inhibiting at least 90% of viral replication in vitro, which demonstrates the potential of these marine natural products to combat infections caused by HMPV in vitro.     

Determination of organophosphorous pesticides in the ppq range using a simple solid-phase extraction method combined with dispersive liquid-liquid microextraction

Solid-phase extraction combined with dispersive liquid-liquid microextraction (SPE-DLLME) was applied for the extraction of six organophosphorous pesticides (OPPs) in water samples. The analytes considered in this study were determined by gas chromatography with mass spectrometry and included prophos, diazinon, chlorpyrifos methyl, methyl parathion, fenchlorphos and chlorpyrifos. Several extraction conditions (extraction solvent and elution/dispersion solvents nature, extraction solvent volume, elution solvent volume, water volume and sample volume) were tested for SPE-DLLME with these analytes and the best results were obtained using carbon tetrachloride as the extraction solvent and acetone as the elution/dispersion solvent. Calibration curves for the determination of OPPs in water samples were constructed in the concentration range of 10-100 ng/L. Limits of detection (LODs) ranged from 38 to 230 pg/L values that are below the maximum admissible level for drinking water (100 ng/L). Relative standard deviations (RSD) were between 8.6 and 10.4% for a fortification level of 100 ng/L. At the same fortification level, the relative recoveries (R.R.) of tap, well and irrigation water samples were in the range of 30.2-97.1%.