Effect of drying conditions during sample pre-treatment on the determination of polycyclic aromatic hydrocarbons in soils

In the context of the entire analytical process, pre-treatment of soil samples is often inadequately considered although the reliability of the results is definitely compromised if the sample is not properly prepared. In this paper, the effect of drying conditions in soil sample pre-treatment on the determination of polycyclic aromatic hydrocarbons (PAHs) has been studied. A systematic approach has been adopted by varying soil type, drying temperatures and solvent polarity to highlight the effect on the analyte recovery; the relationship between PAH molecular structure and their evaporation process from soils is discussed. Experimental data demonstrate that, concerning temperature-assisted drying procedures, PAHs are divided in two distinct groups: PAHs lighter than pyrene, which are seriously affected by drying temperature; and heavier PAHs that can be considered as non-volatile compounds. For studies involving the analysis of lighter PAHs in environmental samples, working on as-received samples is necessary.     

Enantiocomplementary Epoxidation Reactions Catalyzed by an Engineered Cofactor-Independent Non-natural Peroxygenase

Peroxygenases are heme-dependent enzymes that use peroxide-borne oxygen to catalyze a wide range of oxyfunctionalization reactions. Herein, we report the engineering of an unusual cofactor-independent peroxygenase based on a promiscuous tautomerase that accepts different hydroperoxides (t-BuOOH and H₂O₂) to accomplish enantiocomplementary epoxidations of various α,β-unsaturated aldehydes (citral and substituted cinnamaldehydes), providing access to both enantiomers of the corresponding α,β-epoxy-aldehydes. High conversions (up to 98 %), high enantioselectivity (up to 98 % ee), and good product yields (50–80 %) were achieved. The reactions likely proceed via a reactive enzyme-bound iminium ion intermediate, allowing tweaking of the enzyme's activity and selectivity by protein engineering. Our results underscore the potential of catalytic promiscuity for the engineering of new cofactor-independent oxidative enzymes.     

Supramolecular Hierarchy among Halogen‐Bond Donors

Through a combination of structural chemistry, vibrational spectroscopy, and theory, we have systematically examined the relative structure‐directing importance of a series of ditopic halogen‐bond (XB) donors. The molecular electrostatic potential surfaces of six XB donors were evaluated, which allowed for a charge‐based ranking. Each molecule was then co‐crystallized with 21 XB acceptors and the results have made it possible to map out the supramolecular landscape describing the competition between I/Br–ethynyl donors, perfluorinated I/Br donors, and I/Br–phenyl based donors. The results offer practical guidelines for synthetic crystal engineering driven by robust and directional halogen bonds.     

Combining information from headspace mass spectrometry and visible spectroscopy in the classification of the Ligurian olive oils

An electronic nose and an UV-Vis spectrophotometer, in combination with multivariate analysis, have been used to verify the geographical origin of extra virgin olive oils. Forty-six oil samples from three different areas of Liguria were included in this analysis.Initially, the data obtained from the two instruments were analysed separately. Then, the potential of the synergy between these two technologies for testing food authenticity and quality was investigated.Application of Linear Discriminant Analysis, after feature selection, was sufficient to differentiate the three geographical denominations of Liguria (“Riviera dei Fiori”, “Riviera del Ponente Savonese” and “Riviera di Levante”), obtaining 100% success in classification and close to 100% in prediction. The models built using SIMCA as a class-modelling tool, were not so effective, but confirmed that the results improve using the synergy between different analytical techniques.This paper shows that objective instrumental data related to two important organoleptic features such as oil colour and aroma, supply complementary information.     

Background-Free Detection of Spin-Exchange Dynamics at Ultra-Low Magnetic Field

Ultra-low field nuclear magnetic resonance spectroscopy (NMR) and imaging (MRI) inherently suffer from a low signal-to-noise ratio due to the small thermal polarization of nuclear spins. Transfer of polarization from a pre-polarized spin system to a thermally polarized spin system via the Spin Polarization Induced Nuclear Overhauser Effect (SPINOE) could potentially be used to overcome this limitation. SPINOE is particularly advantageous at ultra-low magnetic field, where the transferred polarization can be several orders of magnitude higher than thermal polarization. Here we demonstrate direct detection of polarization transfer from highly polarized ¹²⁹Xe gas spins to ¹H spins in solution via SPINOE. At ultra-low field, where thermal nuclear spin polarization is close to background noise levels and where different nuclei can be simultaneously detected in a single spectrum, the dynamics of the polarization transfer can be observed in real time. We show that by simply bubbling hyperpolarized ¹²⁹Xe into solution, we can enhance ¹H polarization levels by a factor of up to 151-fold. While our protocol leads to lower enhancements than those previously reported under extreme Xe gas pressures, the methodology is easily repeatable and allows for on-demand enhanced spectroscopy. SPINOE at ultra-low magnetic field could also be employed to study ¹²⁹Xe interactions in solutions.     

Purification and characterization of an acetyl esterase fromAspergillus niger

Applied Biochemistry and Biotechnology - Optimized acetyl esterase enzyme production conditions usingAspergillus niger ATCC 10864 in 14-L fermentation jars were determined to be 33?C, 1.5 vvm...     

Asymptotic Analysis of Shell-like Inclusions with High Rigidity

We study the problem of an elastic shell-like inclusion with high rigidity in a three-dimensional domain by means of the asymptotic expansion method. The analysis is carried out in a general framework of curvilinear coordinates. After defining a small real adimensional parameter ε, we characterize the limit problems when the rigidity of the inclusion has order of magnitude \frac1e\frac{1}{\varepsilon } and \frac1e³\frac{1}{\varepsilon^{3}} with respect to the rigidities of the surrounding bodies. Moreover, we prove the strong convergence of the solution of the initial three-dimensional problem towards the solution of the simplified limit problem.     

Characterizations of Sets of Finite Perimeter Using Heat Kernels in Metric Spaces

The overarching goal of this paper is to link the notion of sets of finite perimeter (a concept associated with N^1,1-spaces) and the theory of heat semigroups (a concept related to N^1,2-spaces) in the setting of metric measure spaces whose measure is doubling and supports a 1-Poincaré inequality. We prove a characterization of sets of finite perimeter in terms of a short time behavior of the heat semigroup in such metric spaces. We also give a new characterization of BV functions in terms of a near-diagonal energy in this general setting.     

Influence of temperature and anisotropic pressure on the phase transitions in alpha-cristobalite

The role of temperature and anisotropy of the applied load in the pressure-induced transformations of alpha-cristobalite is investigated by means of first principles molecular dynamics combined with the metadynamics algorithm for the study of solid-solid phase transitions. We reproduce the transition to alpha-PbO2 as found in experiments and we observe that the transition paths are qualitatively different and yield different products when a nonhydrostatic load is applied, giving rise to a new class of metastable structures with mixed tetrahedral and octahedral coordination.