Search results for "DSO"
showing 10 items of 1609 documents
DFT modelling of oxygen adsorption on the Ag-doped LaMnO3 (001) surface
2019
This study was partly financed by the State Education Development Agency of the Republic of Latvia via the Latvian State Scholarship (A.A.) and Latvia-Ukraine Project (Grant LV-UA/2018/2 to E.K.). The work of T.I. is performed under the state assignment of IGM SB RAS. Also, this research was partly supported by the Ministry of Education and Science of the Republic of Kazakhstan in the framework of the scientific and technology Program BR05236795 ‘‘Development of Hydrogen Energy Technologies in the Republic of Kazakhstan’’. The authors thank M. Sokolov for technical assistance and valuable suggestions.
Influence of oxide substrates on monolayer graphene doping process by thermal treatments in oxygen
2019
Abstract The structural and the electronic properties of monolayer graphene made by chemical vapor deposition and transferred on various oxide substrates ( SiO 2 , Al 2 O 3 , and HfO 2 ) are investigated by Raman Spectroscopy and Atomic Force Microscopy in order to highlight the influence of the substrate on the features of p-doping obtained by O 2 thermal treatments. By varing the treatment temperature up to 400 °C, the distribution of the reaction sites of the substrates is evaluated. Their total concentration and the consequent highest doping available is determined and it is shown that this latter is linked to the water affinity of the substrate. Finally, by varing the exposure time to …
Total oxidation of VOCs on Au nanoparticles anchored on Co doped mesoporous UVM-7 silica
2012
Abstract Gold deposited on a cobalt containing siliceous mesoporous structure, UVM-7, presents a good catalytic performance in the total oxidation of propane and toluene. The presence of both gold and cobalt is necessary as bimetallic Au/Co-UVM-7 catalysts are remarkably more active than monometallic Au/UVM-7 or Co-UVM-7 catalysts. The improved activity of the bimetallic AuCo-samples if compared to gold free cobalt catalysts can be explained on the basis of the enhanced reducibility of some cobalt species in the presence of gold, which facilitates the redox cycle. This high reducibility of cobalt species in the bimetallic samples is probably due to the formation of Co 3 O 4 domains at the g…
Preparation of polyelectrolyte-modified membranes for heavy metal ions removal
2017
ABSTRACTPolyethersulfone membranes were modified by polyelectrolyte (PE) multilayers, made of poly(allylamine hydrochloride) with poly(styrene sulfonate), to remove Cu2+, Zn2+ and Ni2+ heavy metal cations from aqueous solutions in a wide range of metal concentration (50–1200 ppm). After characterization of the modified membranes, the efficiency of the process was estimated for single heavy metal ions solution leading to high rejection rates (>90% for 50 ppm) and good adsorption capacities (7.0–8.5 mg cm−2) whatever the metal ion tested. The stability in time of the modified membranes was proved by repeating successive filtrations with the same membrane. The filtration process was also used …
Inorganic nanomaterials in the aquatic environment: behavior, toxicity, and interaction with environmental elements
2016
AbstractThe aim of this paper is to present characteristics, toxicity and environmental behavior of nanoparticles (NPs) (silver, copper, gold, zinc oxide, titanium dioxide, iron oxide) that most frequently occur in consumer products. In addition, NPs are addressed as the new aquatic environmental pollutant of the 21stcentury. NPs are adsorbed onto particles in the aquatic systems (clay minerals, fulvic and humic acids), or they can adsorb environmental pollutants (heavy metal ions, organic compounds). Nanosilver (nAg) is released from consumer products into the aquatic environment. It can threaten aquatic organisms with high toxicity. Interestingly, copper nanoparticles (Cu-NPs) demonstrate…
Study by static SIMS, XPS and UPS of the adsorption of cyanogen on (100) Ni surfaces
2000
Abstract The interaction of cyanogen with (100) Ni surfaces at room temperature was studied using secondary ion mass spectrometry in a static mode, and photoemission spectroscopies (XPS and UPS). It has been shown that cyanogen is adsorbed on this nickel surface in a dissociative mode: atomic carbon and nitrogen are present on the surface as well as CN fragments. These adsorbed species have been characterized by XPS and UPS. Increasing the temperature in the 400 K range increases the rate of the dissociation reaction of CN into atomic carbon and nitrogen. Moreover carbon is found to dissolved into the bulk for temperatures as low as 475 K. No evidence has been found of a polymerized form of…
Adsorption and desorption surface dynamics of gaseous adsorbate on silicate-1 by molecular dynamics simulation
2013
The dynamics of adsorption and desorption of gaseous molecules on the external surface of a crystal and a membrane of zeolite silicate-1 is investigated by molecular dynamics simulation. The gases ...
Sorption of uranium(VI) onto ferric oxides in sulfate-rich acid waters.
2003
The mechanisms of the uranium(VI) sorption on schwertmannite and goethite in acid sulfate-rich solutions were studied by Extended X-ray Absorption Fine Structure (EXAFS) spectroscopy. The samples were prepared under N2 atmosphere and initial uranium(VI) concentrations of 1 x 10(-5) (pH 6.5) to 5 x 10(-5) M (pH 4.2). The ionic strength was adjusted using 0.01 M Na2SO4 or 0.01 M NaClO4, respectively. The EXAFS structural parameters for uranium(VI) sorbed on goethite in sulfate-rich, acid and near-neutral solutions indicate that uranium(VI) forms an inner-sphere, mononuclear, bidentate surface complex. This complex is characterized by a uranium-ferric-iron distance of approximately 3.45 A. Ura…
Predicting the activity of single isolated Lewis acid sites in solid catalysts.
2006
An experimental study of the activity of Ti-, Zr- and Sn-beta catalysts in different types of oxidation reactions is combined with a quantum-chemical analysis of the electronic properties of the active sites and the adsorbed reactants. The differences observed in the catalytic behaviour of the three materials are explained in terms of the molecular orbital distribution of each system. The intrinsic Lewis acid strength of the isolated active site, the degree of back-donation from the catalyst to the empty orbitals of the organic reactant and the net atomic charges on selected atoms are proposed as predictors of reactivity.
Removal of hexavalent chromium from wastewaters by bone charcoal
1999
The adsorption of hexavalent chromium onto bone charcoal was studied as a function of time, amount of charcoal, pH, concentration of chromium and sample volume. The cross interference with other elements was also investigated. Tests were carried out with solutions of chromium(VI) at concentrations between 5 and 25 mg · L–1. Chromium removal efficiencies higher than 90% were achieved at pH = 1 using 2 g of bone charcoal and a stirring time in the order of 30 min. Acid and alkaline pretreatments of bone charcoal did not improve the sorption capacity of bone charcoal against Cr(VI). The presence of other ions had practically no influence on the chromium removal. The presence of a matrix of tan…