Minimal Blocking Sets in PG(2, 8) and Maximal Partial Spreads in PG(3, 8)

We prove that PG(2, 8) does not contain minimal blocking sets of size 14. Using this result we prove that 58 is the largest size for a maximal partial spread of PG(3, 8). This supports the conjecture that q ²–q+ 2 is the largest size for a maximal partial spread of PG(3, q), q>7.     

Shaping of ultrashort pulses using bulk acousto-optic filter

Our paper deals with temporal shaping of ultrashort pulses by direct spectral filtering performed with bulk acousto-optic filters using noncollinear geometry. This geometry allows arbitrary optical pulse repetition rate and high diffraction efficiency at relatively large optical apertures. A theoretical model of the pulse shaper is presented, emphasizing the degrees of freedom in this shaping technique. Phase and angular dispersion effects are analyzed, and experimental results on generating controllable pulse trains are presented. PACS 42.65.Re; 42.79.J     

Microstructural aspects of the hcp-fcc allotropic phase transformation induced in cobalt by ball milling

A detailed correlation between microstructure evolution and allotropic phase transformations occurring in Co when subjected to ball milling has been carried out. After short-term milling, the starting mixture of hcp + fcc Co develops into an almost pure hcp phase. However, for longer milling times, plastic deformation introduces large amounts of stacking faults, especially of twin type, in the hcp structure. As a consequence, some of the hcp Co is converted back into fcc and the hcp unit cell is progressively anisotropically distorted. After long-term milling, a steady 'pseudo-equilibrium' state is observed, where all microstructural parameters, including the fcc percentage, tend to level off. However, the milling intensity can still be adjusted to increase further the stacking-fault probability and, consequently, the amount of fcc Co in the milled powders. The results imply that the stacking-fault formation, rather than the local temperature rise or crystallite size reduction associated with the milling process, is the main mechanism governing the hcp-fcc transformation.     

Thermal Plasma Decomposition of Tetrachloroethylene

Tetrachloroethylene (C₂Cl₄) has been used widely as a solvent and dry cleaning agent, but was later specified as possible human carcinogen. As a result, its safe treatment became a priority. In this paper, we report on its decomposition in an atmospheric radiofrequency thermal plasma reactor. Main components of the exhaust gases were determined by Fourier transform infrared spectroscopy. We found that complete decomposition can be achieved in either oxidative or reductive conditions but not in neutral one. The solid soot product was characterised by transmission electron microscopy and specific surface area measurement. Organic compounds adsorbed on the surface of the soot were extracted by toluene and comprised, based on gas chromatography mass spectrometry, of various perchlorinated aliphatic (for example hexachlorocyclopentadiene) and aromatic compounds (like hexachlorobenzene, octachloronaphthalene or octachloroacenaphthylene). Several nitrogen containing molecules were also identified whose presence are rare during thermal plasma treatments. Further investigation of the extract by mass spectrometry revealed various higher molar mass chlorinated carbon clusters and two types of fullerenes (C₆₀ and C₇₀).     

Double-Slit Interference Pattern from Single-Slit Screen and Its Gravitational Analogues

The double slit experiment (DSE) is known as an important cornerstone in the foundations of physical theories such as Quantum Mechanics and Special Relativity. A large number of different variants of it were designed and performed over the years. We perform and discuss here a new version with the somewhat unexpected results of obtaining interference pattern from single-slit screen. We show using either the Brill’s version of the canonical formulation of general relativity or the linearized version of it that one may find corresponding and analogous situations in the framework of general relativity.     

Non-invasive PGAA,PIXE and ToF-ND analyses on Hungarian Bronze Age defensive armour

Non-invasive, archaeometric analyses on selected Hungarian Bronze Age defensive armour is presented here: three greaves, three helmets two shields as well as one vessel fragment were analysed with PIXE, PGAA and TOF-ND. The detected alloy elemental and phase composition as well as its intergranular or spatial concentration distribution reveals important insights into the alloys used and the manufacturing techniques applied c. 1200–950 BC, and allows to reconstruct the production techniques used during the Late Bronze Age.     

Monitoring the Phosphorylation of Phenol with Diethyl Chlorophosphate in Aqueous Medium in the Presence of Sodium Hydroxide by in Situ Fourier Transform Infrared Spectroscopy

In situ Fourier transform IR spectroscopy has been found to be an appropriate tool for monitoring the title reaction resulting in the formation of diethyl phenylphosphate.     

New insights into the metal ion–peptide hydroxamate interactions: Metal complexes of primary hydroxamic acid derivatives of common dipeptides in aqueous solution

Complex formation of primary dipeptide hydroxamic acids, L-Ala-L-AlaNHOH and L-Ala-L-SerNHOH, as well as the corresponding Z-protected ones, Z-L-Ala-L-AlaNHOH and Z-L-Ala-L-SerNHOH (Z = benzyloxycarbonyl), with iron(III), aluminium(III), nickel(II), copper(II) and zinc(II) was studied in aqueous solution by pH-potentiometric and spectroscopic (UV–Vis, EPR, CD, ¹H NMR) methods. The exclusive formation of [O,O] chelated hydroxamate complexes was found with iron(III) and aluminium(III) with all the ligands. Formation of linkage isomers with the involvement of either [O,O] hydroxamate or [NH₂,CO] chelates was detected both in the zinc(II)-L-Ala-L-AlaNHOH and -L-Ala-L-SerNHOH systems. Upon increasing the pH, none of these chelating sets are capable of preventing the hydrolysis of the metal ion. The formation of stable complexes was found in the nickel(II) and copper(II) systems above pH ∼ 6 with a [NH₂, N_amide, N_hydrox.] binding mode after deprotonation and coordination of the peptide amide and the hydroxamate group. With an excess of copper(II), the formation of trinuclear [Cu₃H_xL₂]^x+4 type (x = −4 to −6) complexes as the major species was also detected. Blocking the terminal amino group in the Z-protected ligands results in a dramatic decrease of the nickel(II) and zinc(II) binding strengths, and insoluble complexes with copper(II). No indication was found for the role of the hydroxyl group of the serine moiety in metal ion binding.     

Identification strategy for unknown pollutants using high-resolution mass spectrometry: Androgen-disrupting compounds identified through effect-directed analysis

Effect-directed analysis has been applied to a river sediment sample of concern to identify the compounds responsible for the observed effects in an in vitro (anti-)androgenicity assay. For identification after non-target analysis performed on a high-resolution LTQ-Orbitrap, we developed a de novo identification strategy including physico-chemical parameters derived from the effect-directed analysis approach. With this identification strategy, we were able to handle the immense amount of data produced by non-target accurate mass analysis. The effect-directed analysis approach, together with the identification strategy, led to the successful identification of eight androgen-disrupting compounds belonging to very diverse compound classes: an oxygenated polyaromatic hydrocarbon, organophosphates, musks, and steroids. This is one of the first studies in the field of environmental analysis dealing with the difficult task of handling the large amount of data produced from non-target analysis. The combination of bioassay activity assessment, accurate mass measurement, and the identification and confirmation strategy is a promising approach for future identification of environmental key toxicants that are not included as priority pollutants in monitoring programs.