Method for detecting and characterising actinide-bearing micro-particles in soils and sediment of the Fukushima Prefecture,Japan

An aqueous biphasic system has been used for selective extraction of U(VI) ions from Th(IV), Sm(III) and Ce(III). Role of different biomolecules like morin, catechin, hesperidin and 4-hydroxycoumarin have been studied. Morin serves as the best reagent when citrate ions are used as a masking agent. Citrate forms stronger complexes with the other metal ions than morin thereby restricting their extractions. Contrarily, U(VI) forms a stronger complex with morin than citrate and is selectively extracted under the same conditions. It was also observed that morin can act as a spectrophotometric reagent for ratiometric detection and analysis of U(VI) ions.

     

Time resolved spectral interferometry for single shot femtosecond characterization

Time resolved spectral interferometry is applied to femtosecond pulse coherent measurement. A new configuration that can be directly applied to single shot detection is presented. The efficiency of this self-referenced real-time passive technique is experimentally demonstrated during the characterization of chirped pulses. Additionally, we quantitatively retrieve the spectral phase shift which is associated to the propagation through a F4 glass parallel plate. Numerical results are also reported showing examples of complex pulse characterization. Finally, limitations of the technique are discussed.     

Tunable picosecond UV source at 10 kHz based on an all-solid-state diode-pumped laser system

4 laser. The amplified pulses were frequency-converted in the blue and in the UV by harmonic generation (doubling and tripling) in two lithium triborate (LBO) crystals. Received: 11 March 1997/Accepted: 24 April 1997     

Polarization-multiplexed x((2)) solitary-wave interactions

We investigate interactions between vectorial solitary waves through typeII second-harmonic generation. We demonstrate that one can tune the collision distance of two initially codirectional solitary waves changing their polarization state. Moreover, by adiabatic perturbation analysis, it is possible to predict such a collision distance as a function of solitary-wave separation, in good agreement with numerical simulations.     

Large spin, magnetically anisotropic, octametallic vanadium(iii) clusters with strong ferromagnetic coupling

Syntheses, structural and magnetic and EPR data are reported for two octametallic V(III) clusters with anisotropic S = 4 ground states arising from strong ferromagnetic exchange interactions.     

Recent trends in perfluorinated sulfoximines

The search for original perfluorinated moieties is a very modern and attractive challenge. Among the emergent groups, the S-perfluoroalkylated sulfoximines are very peculiar because of their structural diversity and promising properties. A literature survey shows that interest in these molecules is strongly increasing. This short review summarizes the recent works devoted to this topic.     

Identification and quantification of domoic acid by UHPLC/QTOF tandem mass spectrometry,with simultaneous identification of non-target photodegradation products

Amnesic shellfish poisoning is a potentially lethal human toxic syndrome which is caused by domoic acid (DA), a neurotoxin produced by marine phytoplankton, principally from Pseudonitzschia genus. In this report, a method to identify and quantify the DA toxin, with simultaneous identification of its photodegradation products, has been developed. It uses an ultra high performance liquid chromatography coupled to a quadrupole-time-of-flight tandem mass spectrometer (UHPLC–QTOF) after solid-phase extraction (SPE). An unambiguous identification of DA was carried out by considering both the retention time of DA in UHPLC and the exact mass of protonated DA molecule ([M + H]⁺ = 312.1447 m/z) and of the most intense fragment ion (m/z 266.1391). The quantification was conducted using protonated DA molecule with protonated Glafenin as internal standard, obtaining a limits of detection of 0.75 µg L^?1. Large screening with UHPLC–QTOF could also give structural information about degradation products of DA present in samples after UV-irradiation. This method was applied for the determination of DA in complex liquid samples after SPE and is applicable for environmental monitoring of this toxic substance in the aquatic environment.     

A facile synthetic route to new pyrazoloisoindolones

A facile method for the synthesis of new pyrazoloisoindolones via a Suzuki cross-coupling reaction using a pyrazolylboronic ester is described.     

Variational Convergences of Dual Energy Functionals for Elastic Materials with a ε-Thin Strong Inclusion

We give a new derivation, based on the complementary energy formulation, of a simplified model for a multi-structure made up of two anisotropic hyper-elastic bodies connected by a thin strong material layer. The model is obtained by identifying the Mosco-limit of the stored complementary energy functional when the thickness is of order ?? and the stiffness of order 1/?? where ?? is a positive real adimensional parameter. In order to prove the existence of the displacement associated with the stress we use a suitable weak version of the Saint-Venant compatibility condition also known as Donati??s theorem.     

Spectroscopic, magnetochemical, and crystallographic study of cesium iron phosphate hexahydrate: characterization of the electronic structure of the iron(II) hexa-aqua cation in a quasicubic environment

Spectroscopic, magnetochemical, and crystallographic data are presented for CsFe(H2O)6PO4, a member of a little-known isomorphous series of salts that facilitates the study of hexa-aqua ions in a quasicubic environment. Above 120 K, the deviations from cubic symmetry are minimal, as shown by the first example of an iron(II) M?ssbauer spectrum that exhibits no measurable quadrupole splitting. Two crystallographically distinct [Fe(OH2)6]2+ complexes are identified from inelastic neutron-scattering (INS) experiments conducted between 2 and 15 K. The data are modeled with the ligand-field Hamiltonian, H = lambdaL? + betaB(kL + 2?) + Delta(tet){Lz2 - (1/3)L(L + 1)} + Delta(rhom){Lx2 - Ly2}, operating in the ground-term (5)T(2g) (Oh) basis. An excellent reproduction of INS, M?ssbauer, HF-EPR, and magnetochemical data are obtained in the 2 and 15 K temperature regimes with the following parameters: lambda = -80 cm(-1); k = 0.8; site A Delta(tet) = 183 cm(-1), Delta(rhom)= 19 cm(-1); site B Delta(tet) = 181 cm(-1), Delta(rhom)= 12 cm(-1). The corresponding zero-field-splitting (ZFS) parameters of the conventional S = 2 spin Hamiltonian are as follows: site A D = 12.02 cm(-)(1), E = 2.123 cm(-1); site B D = 12.15 cm(-1), E = 1.37 cm(-1). A theoretical analysis of the variation of the energies of the low-lying states with respect to displacements along selected normal coordinates of the [Fe(OH2)6]2+, shows the zero-field splitting to be extremely sensitive to small structural perturbations of the complex. The expressions derived are discussed in the context of spin-Hamiltonian parameters reported for the [Fe(OH2)6]2+ cation in different crystalline environments.