Laser desorption/ionization coupled to tandem mass spectrometry for real-time monitoring of paraquat on the surface of environmental particles

Aerosol mass spectrometry with laser desorption/ionization was investigated as a possible tool for real-time monitoring of the presence of the pesticide paraquat on the surface of airborne soil particles. Laser desorption/ionization of paraquat dication produced only singly charged ions. The most abundant species were [M](+.), [M - H](+), and [M - CH3](+). Operation of the ion trap mass spectrometer in the MS(3) mode allowed the reduction of the signal dependence on laser fluence fluctuations and permitted the detection of the analyte with good sensitivity and high selectivity. The estimated limit of detection in terms of surface coverage was 0.016 monolayers, approximately 1 attomole of paraquat on the surface of a single micron-sized soil particle.     

Near varieties of idempotent generated completely simple semigroups

Algebra universalis - Completely simple semigroups form a variety if we consider them as algebras with multiplication and inversion. A near variety of idempotent generated completely simple...     

Minimal coupling in spin-2 field

It is shown that the spin-2 Lagrangian of Watanabe and Bhargava can be generalised by the introduction of a real parameter b associated with derivative ordering. After minimal coupling the spin-2 dynamical equations of Nath and Velo and Zwanziger can be derived as special cases. The constraint situation in these equations is then summarised and related to the first-order Lagrangian approach of Federbush, Chang, et al. Only one value of the parameter b gives a correct manifold of states after coupling. Finally it is shown that the auxiliary field approach to spin-2 proposed by Chang is dynamically inconsistent under minimal coupling.     

Wasserstoff-Adsorption an Ti3Al

Ohne Zusammenfassung     

Higher order speciation effects on plutonium L(3) X-ray absorption near edge spectra

Pu L(3) X-ray near edge absorption spectra for Pu(0-VII) are reported for more than 60 chalcogenides, chlorides, hydrates, hydroxides, nitrates, carbonates, oxy-hydroxides, and other compounds both as solids and in solution, and substituted in zirconolite, perovskite, and borosilicate glass. This large database extends the known correlations between the energy and shape of these spectra from the usual association of the XANES with valence and site symmetry to higher order chemical effects. Because of the large number of compounds of these different types, a number of novel and unexpected behaviors are observed, such as effects resulting from the medium and disorder that can be as large as those from valence.     

The mechanical response of core-shell structures for nanoporous metallic materials

Nanoporous gold (NP-Au) exhibits microscale plasticity, but macroscopically fails in a relatively brittle manner. This current study suggests that a core-shell structure can increase both ductility and strength of NP-Au. A core Au foam structure was created using conventional dealloying methods with average ligament size of 60?nm. Nickel was then electroplated on to the NP-Au with layer thicknesses ranging from 2.5?nm to 25?nm. Nanoindentation demonstrated a significant increase in the hardness of the coated Np-Au, to about five times of that of the pure Np-Au, and a decrease in creep by increasing the thickness of the coated Ni layer. Molecular dynamics simulations of Au–Ni ligaments show the same trend of strengthening behavior with increasing Ni thickness suggesting that the strengthening mechanisms of the Np-Au are comparable to those for fcc nano ligaments. The simulations demonstrate two different strengthening mechanisms with the increased activity of the twins in plated Au–Ni ligaments, which leads to more ductile behavior, as opposing to the monolithic Au ligaments where nucleation of dislocations govern the plasticity during loading.