Macroscopic and spectroscopic analysis of lanthanide adsorption to bacterial cells

This study was designed to combine surface complexation modelling of macroscopic adsorption data with X-ray Absorption Spectroscopic (XAS) measurements to identify lanthanide sorption sites on the bacterial surface. The adsorption of selected representatives for light (La and Nd), middle (Sm and Gd) and heavy (Er and Yb) lanthanides was measured as a function of pH, and biomass samples exposed to 4 mg/L lanthanide at pH 3.5 and 6 were analysed using XAS. Surface complexation modelling was consistent with the light lanthanides adsorbing to phosphate sites, whereas the adsorption of middle and heavy lanthanides could be modelled equally well by carboxyl and phosphate sites. The existence of such mixed mode coordination was confirmed by Extended X-ray Absorption Fine Structure (EXAFS) analysis, which was also consistent with adsorption to phosphate sites at low pH, with secondary involvement of carboxyl sites at high adsorption density (high pH). Thus, the two approaches yield broadly consistent information with regard to surface site identity and lanthanide coordination environment. Furthermore, spectroscopic analysis suggests that coordination to phosphate sites is monodentate at the metal/biomass ratios used. Based on the best-fitting pKa site, we infer that the phosphate sites are located on N-acetylglucosamine phosphate, the most likely polymer on gram-negative cells with potential phosphate sites that deprotonate around neutral pH

Site multiplicity of rare earth ions in III-nitrides

This presentation reviews recent lattice location studies of RE ions in GaN by electron emission channelling (EC) and X-ray absorption fine structure (XAFS) techniques. These studies agree that RE ions at low concentrations (whether they are incorporated during growth or introduced later by ion implantation) predominantly occupy Ga substitutional sites, as expected from considerations of charge equivalence. We combine this result with some examples of the welldocumented richness of optical spectra of GaN:RE3+ to suggest that the luminescence of these materials may be ascribed to a family of rather similar sites, all of which feature the REGa defect

Fabrication, defect chemistry and microstructure of Mn-doped UO2

Mn-doped UO2 is under consideration for use as an accident tolerant nuclear fuel. We detail the synthesis of Mn-doped UO2 prepared via a wet co-precipitation method, which was refined to improve the yield of incorporated Mn. To verify the Mn-doped UO2 defect chemistry, X-ray absorption spectroscopy at the Mn K-edge was performed, in addition to X-ray diffraction, Raman spectroscopy and high-energy resolved fluorescence detection X-ray absorption near edge spectroscopy at the U M4-edge. It was established that Mn2+ directly substitutes for U4+ in the UO2 lattice, accompanied by oxygen vacancy (Ov) charge compensation. In contrast to other divalent-element doped UO2 materials, compelling evidence for U5+ in a charge compensating role was not found. This work furthers understanding of the structure and crystal chemistry of Mn-doped UO2, which could show potential advantages as a novel efficient advanced nuclear fuel

Controlled fabrication of osmium nanocrystals by electron, laser and microwave irradiation and characterisation by microfocus X-ray absorption spectroscopy

YesOsmium nanocrystals can be fabricated by electron (3–50 nm, formed by atom migration), 785–815 nm laser (20–50 nm, in micelle islands), and microwave (ca. 1 nm in arrays, >100 mg scale) irradiation of a polymer-encapsulated OsII carborane; microfocus X-ray absorption studies at the Os LIII-edge show differences between the three preparation methods, suggesting that the electron-beam irradiated materials have a significant support interaction and/or surface oxidation, while the laser and microwave samples are more like metallic osmium.Royal Society (University Research Fellowship No. UF150295 to NPEB), the Leverhulme Trust (Early Career Fellowship No. ECF-2013-414 to NPEB), the ERC (Grant No. 247450 to PJS), EPSRC (Grant No. EP/F034210/1 to PJS and EP/ J007153/1 to VGS), Diamond Light Source (Beam-time grant number SP11314)

Neptunium and uranium interactions with environmentally and industrially relevant iron minerals

Neptunium (237Np) is an important radionuclide in the nuclear fuel cycle in areas such as effluent treatment and the geodisposal of radioactive waste. Due to neptunium’s redox sensitivity and its tendency to adsorb strongly to mineral phases, such as iron oxides/sulfides, the environmental mobility of Np can be altered significantly by a wide variety of chemical processes. Here, Np interactions with key iron minerals, ferrihydrite (Fe5O8H·4H2O), goethite (α-FeOOH), and mackinawite (FeS), are investigated using X-ray Absorption Spectroscopy (XAS) in order to explore the mobility of neptunyl(V) (Np(V)O2+) moiety in environmental (radioactive waste disposal) and industrial (effluent treatment plant) scenarios. Analysis of the Np LIII-edge X-ray Absorption Near-Edge Structure (XANES) and Extended X-ray Absorption Fine Structure (EXAFS) showed that upon exposure to goethite and ferrihydrite, Np(V) adsorbed to the surface, likely as an inner-sphere complex. Interestingly, analysis showed that only the first two shells (Oax and Oeq) of the EXAFS could be modelled with a high degree of confidence, and there was no clear indication of Fe or carbonate in the fits. When Np(V)O2+ was added to a mackinawite-containing system, Np(V) was reduced to Np(IV) and formed a nanocrystalline Np(IV)O2 solid. An analogous experiment was also performed with U(VI)O22+, and a similar reduction was observed, with U(VI) being reduced to nanocrystalline uraninite (U(IV)O2). These results highlight that Np(V) may undergo a variety of speciation changes in environmental and engineered systems whilst also highlighting the need for multi-technique approaches to speciation determination for actinyl (for example, Np(V)O2+) species

An XAS Study of the Semi-Conducting Sulfides M2S3 (M = As, Sb, Bi)

XANES has been used to probe the low-lying vacant states in the Period 15 sulfide semi-conductors M2S3 (M = As, Sb, Bi). The As K- and L3-, Sb K- and L3-, and Bi L3- and L1-edges are related to the S K-edge XANES in terms of bands of mixed orbital character. In the K-edge spectra transitions from the 1s state to states of some p character can be seen in the region between 5 eV before the edge and 15 eV after it. The S spectra are alike showing the similar nature of the electronic structure of these compounds. The white line intensity decreases down the period showing the density of empty S 2p states at the Fermi level is also decreasing. The Period 15 spectra are related to theoretical band structure calculations for As2S3

Application of microfocus x-ray beams from synchrotrons in heritage conservation

Synchrotron-based techniques are becoming increasingly important in heritage science and the aim of this article is to describe how recently developed microfocus methods can probe the elemental composition, speciation and structure at the micron level in samples from structures. Firstly an outline is given of the major techniques that are used, namely x-ray fluorescence, diffraction and absorption spectroscopy, and the information that they can provide. This is followed by a description of the experimental set-up and procedures. The application of the methods is exemplified by case studies of the degradation of three types of historic structural materials; marble, glass and ship timbers. The results of the studies and their role in developing conservation strategies are described. © 2012 Copyright Taylor and Francis Group, LLC

Correlating metal poisoning with zeolite deactivation in an individual catalyst particle by chemical and phase sensitive X-ray microscopy

Fluid catalytic cracking (FCC) is the main conversion process used in oil refineries. An X-ray microscopy method is used to show that metal poisoning and related structural changes in the zeolite active material lead to a non-uniform core–shell deactivation of FCC catalyst particles. The study links the detrimental effect of V and Ni poisoning with zeolite destruction and dealumination in a spatial manner within a single FCC catalyst particle