Experimental study of atmospheric pressure surface discharge in helium

The surface discharge generated at atmospheric pressure in helium was examined by monitoring the current and voltage atthe discharge electrode. The discharge generated in helium behaves differently when compared to that generated in other gases (e.g. air). The single discharge duration and the time between consecutive discharges are longer because there is a different mechanism of discharge evolution. The metastable helium atoms play the most important role for discharge generation. Streamer-like and glow types of discharge were observed. The decay of helium metastables concentration determines the discharge regime. Hence, operation conditions have strong influence on the discharge regime. The introduction of gas flow removes metastable quenchers /gaseous products from dielectric and electrode surfaces) and transition to glow discharge is observed. Also covering the discharge electrode with thin dielectric foil to suppress Auger de-excitation of metastables at metal surface leads to generation of atmospheric pressure glow surface discharge. Properties of this discharge are comparable with properties of glow discharge at low pressure (e.g. the electron concentration).     

In situ co-adsorption of arsenic and iron/manganese ions on raw clays

The use of clays as effective arsenic sorbents has been strongly limited due to their low pH_ZPC and cation active behaviour in aqueous systems at pH > 3.5. A simple Fe/Al/Mn pre-treatment can significantly improve their sorption affinity to oxyanions, including arsenites and arsenates. The dynamics of arsenic adsorption from groundwater is also controlled by dissolved Fe/Mn ions, which behave as promoters of As adsorption, or competitors to adsorption sites. Low grade calcinated kaolin (MT) and bentonite (BT) were used as clay sorbents. Arsenic adsorption on raw clays without presence of Fe/Mn ions is very slow and limited. During co-adsorption the Fe/Mn ions and As oxyanions were adsorbed together onto a sorbent surface. Both Mn and Fe particles demonstrated a good sorption affinity to the clay surface, but only Fe particles supported As adsorption considerably (80% of As were removed in Fe/As system, while < 30% only in the Mn/As system). The kinetics of co-adsorption compared to the use of Fe/Mn pre-modified sorbents indicated a more dynamic process, while all mechanisms corresponded to the first order run (k ≈ 9.10^− 6- 1.10^− 4 s^− 1). Arsenic was strongly stabilized in pre-modified sorbents.     

Chalcogenide coatings of Ge15Sb20S65 and Te20As30Se50

Chalcogenide coatings are investigated to obtain either optical components for spectral applications or optochemical sensors in the mid-infrared. The deposition of Ge(15)Sb(20)S(65) and Te(20)As(30)Se(50) chalcogenide glasses is performed by two physical techniques: electron-beam and pulsed-laser deposition. The quality of the film is analyzed by scanning electron microscopy, atomic force microscopy, and energy dispersive spectroscopy to characterize the morphology, topography, and chemical composition. The optical properties and optical constants are also determined. A CF(4) dry etching is performed on these films to obtain a channeled optical waveguide. For a passband filter made by electron-beam deposition, cryolite as a low-refractive-index material and chalcogenide glasses as high-refractive-index materials are used to favor a large refractive-index contrast. A shift of a centered wavelength of a photosensitive passband filter is controlled by illumination time.     

Pyrazinium Salts as Efficient Organocatalysts of Mild Oxidations with Hydrogen Peroxide

A series of 3‐substituted pyrazinium tetrafluoroborates was prepared as simple analogues of flavinium salts which are efficient organocatalysts for oxidations with hydrogen peroxide. It was shown that pyrazinium derivatives with an electron‐withdrawing substituent catalyze mild oxidations of sulfides to sulfoxides and Baeyer–Villiger oxidations in a similar way to flavinium catalysts. The most reactive catalyst, 3‐cyanopyrazinium tetrafluoroborate, was efficiently employed in preparative sulfoxidations of aromatic and aliphatic sulfides as well as in Baeyer–Villiger oxidations of cyclobutanones. A proposed mechanism for the catalysis is based on the formation of pyrazine hydroperoxide which is the agent oxidizing the substrate.