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Year-long measurements of C1-C3 halocarbons at an urban site and their relationship with meteorological parameters
M Anwar K Khan, M Iqbal Mead, Iain R. White, Ben Golledge, Graham Nickless, Alan Knights, Damien Martin, Alison C Rivett, Brian G R Greally, Dudley E Shallcross, 2009, original scientific article

Abstract: The mixing ratios of 11 C1–C3 halocarbons have been measured using a GC–twin‐linked ECD system over the period from October 2004 to December 2005 at an urban site in Bristol, UK. Time series and seasonal variations of the halocarbons were analysed over the period to determine biogenic and anthropogenic sources and sinks. Correlations between the target halocarbons were also observed, suggesting common sources within the area. Wind rose plots for all halocarbons have been used to assist in the determination of halocarbons sources. Halocarbon concentrations are highest at low‐wind speeds and decrease as wind speed increases, a few species (CCl4 and CH3Cl most notably) rise at very high‐wind speeds suggesting release from the Bristol Channel.
Keywords: adsorption–desorption system, anthropogenic halocarbons, biogenic halocarbons, electron capture detector, gas chromatography, methyl bromide
Published in RUNG: 18.07.2019; Views: 2879; Downloads: 0
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24.
Stable carbon isotope analysis of selected halocarbons at parts per trillion concentration in an urban location
M Iqbal Mead, M Anwar H Khan, Ian D Bull, Iain R. White, Graham Nickless, Dudley E Shallcross, 2008, original scientific article

Abstract: ∂13C values of a suite of halocarbons have been determined in an urban background site in Bristol, UK. A novel mobile preconcentration system, based on the use of multi-adsorbent sample tubes, has been developed for trapping relatively large-volume air samples in potentially remote areas. An Adsorption Desorption System-Gas Chromatography-Electron Capture Detector was used to measure the mixing ratios of the selected halocarbon species, while a Gas ChromatographyCombustionIsotope Ratio Mass Spectrometer was used to determine ∂13C values. For the species with strong local sources, the variation of isotope ratios has been observed over the experimental period. Some of the results reported in the present study differ from previously reported values and reasons for this are discussed. The reporting of different ∂13C values for selected halocarbons from different areas in the present study suggests that ∂13C values may be used to determine the relative magnitudes of anthropogenic and biogenic sources.
Keywords: Adsorption Desorption System (ADS), Automated Thermal Desorber (ATD), Electron Capture Detector (ECD), Gas Chromatography (GC), Isotope Ratio Mass Spectrometry (IRMS)
Published in RUNG: 18.07.2019; Views: 3035; Downloads: 0
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25.
Oxalic acid adsorption states on the clean Cu(110) surface
Sara Fortuna, 2016, original scientific article

Abstract: Carboxylic acids are known to assume a variety of configurations on metallic surfaces. In particular oxalic acid on the Cu(110) surface has been proposed to assume a number of upright configurations. Here we explore with DFT calculations the possible structures that oxalic acid can form on copper 110 at different protonation states, with particular attention at the possibility of forming structures composed of vertically standing molecules. In its fully protonated form it is capable of anchoring itself on the surface thanks to one of its hydrogen-free oxygens. We show the monodeprotonated upright molecule with two oxygens anchoring it on the surface to be the lowest energy conformation of a single oxalic molecules on the Cu(110) surface. We further show that it is possible for this configuration to form dense hexagonally arranged patterns in the unlikely scenario in which adatoms are not involved.
Keywords: oxalic acid, oxalate, cu(110), copper, surface, adsorption, density functional theory, DFT
Published in RUNG: 11.10.2016; Views: 4440; Downloads: 0
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26.
Removal of manganese in batch and fluidized bed systems using beads of zeolite a as adsorbent
Mina Jovanovic, Iztok Arčon, Janez Kovač, Nataša Novak Tušar, Bojana Obradovic, Nevenka Rajić, 2016, original scientific article

Abstract: In this study the uptake capacity of Mn(II) ions by zeolite A beads was investigated for different initial Mn concentration (100e400 mg Mn dm^-3) in batch mode at 25e55 C. The obtained adsorption capacity varying from 30 to 50 mg Mn g^-1 demonstrated a high affinity of zeolite A towards Mn(II) present in solutions. Kinetic studies indicated the intra-particle diffusion as the rate limiting step up to 45 C with apparent diffusivities in the range (1.2e2.0) x 10^-13 m2 s^-1 and the activation energy of 21.9 kJ mol^-1, which implies strong interactions between the zeolite A and Mn ions. At 55 C ion-exchange became the rate limiting step. The adsorption isotherms were studied at 25 C showing that the Mn adsorption is the best described by the Langmuir model suggesting a homogenous zeolite surface. XPS analysis of the Mnloaded beads showed that there is no surface accumulation of Mn but an almost uniform Mn distribution inside zeolite A, whereas XANES and EXAFS suggested that the adsorption of Mn(II) was followed by the Mn(II) oxidation and oxide formation. Regeneration of the spent zeolite was examined in 8 adsorption/desorption cycles by a chelating Na2EDTA in a fluidized column. It has been found that zeolite A beads could be reused for at least 4 cycles with satisfactory Mn(II) adsorption efficiencies of about 70%.
Keywords: Zeolite A Manganese Adsorption kinetics EXAFS/XANES XPS
Published in RUNG: 01.04.2016; Views: 5178; Downloads: 0
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