States of surface V(IV)-bearing groups in phosphorus-vanadium oxide and titanium-vanadium oxide silica gels made by molecular epitaxy

ESR shows that V(IV) may occur in isolated or interacting vanadium-oxygen groups on the surfaces of catalytically active P-V and Ti-V-bearing silica gels; there is a relationship between the V(IV) content and the phthalic anhydride selectivity in the oxidation of o-xylene.Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 28, No. 3, pp. 277–282, May–June, 1992.     

Surface characterization of fluorinated polymers (PTFE, PVDF, PFA) for use in ultratrace analysis

Surface characterization of new unused PTFE, PFA and PVDF labware has been carried out by light microscopy, scanning electron microscopy, profilometry and atomic force microscopy. It has been found that in spite of higher micro-roughness, PFA exhibits the lowest nano-roughness and hence seems best suited as vessel material for relatively mild pressureless chemical operations for sample preparation of ultrapure substances, as container material for storage of ultrapure liquids, and for transport of such liquids, e.g., from the producer in the chemical to the end user in the microelectronics industry. This suitability refers only to the surface quality of the investigated materials. PTFE-surfaces, due to the sintering process of production, exhibit the most unfavourable surface quality of the investigated fluorinated polymers.     

General method for the liquid-liquid extraction of molybdenum and its application to neutron activation analysis

Summary The liquid-liquid extraction of Mo(VI) from different acid solutions by zinc diethyldithiocarbamate in chloroform is described. This extractant allows the separation of nanogram to milligram quantities of Mo from even gram quantities of many other elements. The separation of Mo can be made selective by appropriate choice of the composition of the aqueous phase, by back-extraction of Mo and/or the coextracted elements, and by masking Mo with hydrogen peroxide. These techniques were adapted for the determination of Mo in several reference materials by radiochemical neutron activation analysis via ⁹⁹Mo.     

Radioanalytical monitoring of the formation of barium sulfate in aqueous solutions

The formation of barium sulfate in aqueous media causes problems of insoluble scale formation. On the other hand, the coprecipitation of uranium and transuranium elements with barium sulfate has been suggested for the determination of these elements in environmental monitoring processes. Therefore, the study of barium sulfate crystal growth is required. The investigations done so far suffer from the low sensitivity of the analytical methods used. In the present work we have overcome this problem by using¹³¹Ba for the preparation of supersaturated solutions. Thus kinetics parameters such as induction time and precipitation rates were measured. The polynuclear mechanism was found to be operative at high and the spiral growth at low supersaturations.