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.     

Mouse homologues of the human AZF candidate gene RBM are expressed in spermatogonia and spermatids, and map to a Y chromosome deletion interval associated with a high incidence of sperm abnormalities

By fusing the genes encoding green fluorescent protein (GFP) and beta-glucuronidase (GUS) we have created a set of bifunctional reporter constructs which are optimized for use in transient and stable expression studies in plants. This approach makes it possible to combine the advantage of GUS, its high sensitivity in histochemical staining, with the advantages of GFP as a vital marker. The fusion proteins were functional in transient expression studies in tobacco using either DNA bombardment or potato virus X as a vector, and in stably transformed Arabidopsis thaliana and Lotus japonicus plants. The results show that high level of expression does not interfere with efficient stable transformation in A. thaliana and L. japonicus. Using confocal laser scanning microscopy we show that the fusion constructs are very suitable for promoter expression studies in all organs of living plants, including root nodules. The use of these reporter constructs in the model legume L. japonicus offers exciting new possibilities for the study of the root nodulation process.     

The effect of linker of electrodes prepared from sol–gel ionic liquid precursor and carbon nanoparticles on dioxygen electroreduction bioelectrocatalysis

The effect of linker of three-dimensional, hydrophilic-carbon-nanoparticle film-electrodes prepared by layer-by-layer method on redox probe accumulation and bioelectrocatalytic dioxygen reduction was studied and compared for two different electrode scaffolds. The linker in both of these scaffolds was based on the same ionic liquid sol–gel precursor, 1-methyl-3-(3-trimethoxysilylpropyl) imidazolium bis(trifluoromethyl-sulfonyl)imide. The first electrode type was prepared by alternative immersion of tin doped indium oxide substrate in an aqueous suspension of carbon nanoparticles modified with phenyl sulphonic groups and a sol composed of ionic liquid sol–gel precursor and tetramethoxysilane. For the second electrode type sol was replaced by a methanolic suspension of silicate submicroparticles with appended imidazolium functional groups. In both films 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonate) anions accumulate irreversibly. In the case of the first electrode electrostatic attraction plays the more important role in comparison to the case of the second where stable adsorption of the redox probe takes place. After adsorption of bilirubin oxidase, electrodes obtained from sol and carbon nanoparticles exhibit modest bioelectrocatalytic activity towards dioxygen reduction at pH 4.8, however those obtained from oppositely charged particles are much more efficient. The magnitude of the associated catalytic current in both cases depends on the number of immersion and withdrawal steps. Interestingly, mediatorless catalysis at electrodes obtained from oppositely charged particles is more efficient than mediated catalysis.     

Switching the electrical resistance of individual dislocations in single-crystalline SrTiO3

The great variability in the electrical properties of multinary oxide materials, ranging from insulating, through semiconducting to metallic behaviour, has given rise to the idea of modulating the electronic properties on a nanometre scale for high-density electronic memory devices. A particularly promising aspect seems to be the ability of perovskites to provide bistable switching of the conductance between non-metallic and metallic behaviour by the application of an appropriate electric field. Here we demonstrate that the switching behaviour is an intrinsic feature of naturally occurring dislocations in single crystals of a prototypical ternary oxide, SrTiO(3). The phenomenon is shown to originate from local modulations of the oxygen content and to be related to the self-doping capability of the early transition metal oxides. Our results show that extended defects, such as dislocations, can act as bistable nanowires and hold technological promise for terabit memory devices.     

Activity of selenium modified ruthenium-electrodes and determination of the real surface area

The determination of the surface area of Pt and Ru electrocatalyst surfaces by oxidation of adsorbed CO and by oxidation of a Cu upd layer are compared. The amount of adsorbed CO was determined mass-spectrometrically from the ionic current for CO₂ formation during an oxidative potential sweep. On Ru, the Faradaic charge is too large (by approx. 55%) due to Faradaic effects (oxygen adsorption). For massive Ru electrodes a Cu upd charge of 520 μC cm⁻² is found after normalization to the area determined by CO oxidation. Using this value, both methods yield identical surface areas for nanoparticulate Ru catalysts. On Ru surfaces (both massive and nanoparticulate) completely covered by Se the amount of Cu upd charge decreases to one fourth of the value observed for pure Ru. Since CO is only adsorbed on free Ru sites and not on Se covered sites, the oxidation charge for the latter can be used to determine the number of free Ru sites, whereas the decrease of the Cu upd charge on Se modified surfaces can be used to calculate the area which is modified by Se. This method, previously tested on the model electrodes, was extended to Ru nanoparticle and Ru/Se electrodes. Using this surface determination it is possible to draw conclusions about the active surface area and the Se composition of the outer shell of Ru/Se nanoparticles. For the first time we also show, using RRDE measurements, that the oxygen reduction reaction is enhanced by simple Se adsorption also on massive Ru. It could be shown that the activity for the Ru/Se electrode increases with the Se amount on the surface.     

Segmentation and supervised classification of image objects in Epo doping-control

A software system Gel Analysis System for Epo (GASepo) has been developed within an international WADA project. As recent WADA criteria of rEpo positivity are based on identification of each relevant object (band) in Epo images, development of suitable methods of image segmentation and object classification were needed for the GASepo system. In the paper we address two particular problems: segmentation of disrupted bands and classification of the segmented objects into three or two classes. A novel band projection operator is based on convenient object merging measures and their discrimination analysis using specifically generated training set of segmented objects. A weighted ranks classification method is proposed, which is new in the field of image classification. It is based on ranks of the values of a specific criterial function. The weighted ranks classifiers proposed in our paper have been evaluated on real samples of segmented objects of Epo images and compared to three selected well-known classifiers: Fisher linear classifier, Support Vector Machine, and Multilayer Perceptron.

Biological properties of copolymer of 2-Hydroxyethyl methacrylate with sulfopropyl methacrylate

Interaction of organism with non-toxic implanted polymers depends on the physicochemical properties of the implant surface, which influence the adsorption of bioactive proteins and subsequently adhesion and growth of cells. The synthetic hydrogels are known as poorly adhesive surfaces. In this study we demonstrated the adsorption of albumin, fibrinogen, fibronectin, basic fibroblast growth factor, heparin-binding epidermal growth factor-like growth factor and epidermal growth factor to poly(2-hydroxyethyl methacrylate) (pHEMA) and copolymer of 2-hydroxyethyl methacrylate (HEMA) and potassium salt of 3-sulfopropyl methacrylate (SPMAK). The adhesion and growth of 3T3 cells and human keratinocytes on surface of these polymers was tested without and with pretreatment of polymers with heparin-binding epidermal growth factor-like growth factor. The adhesion of mixture of human granulocytes and monocytes to these surfaces was also tested. The strips of both polymers were subcutaneously and intracerebrally implanted into the rat and the extent of foreign body reaction and brain biocompatibility was evaluated. The results showed the extensive adsorption of basic fibroblast growth factor and heparin-binding epidermal growth factor-like growth factor to copolymer containing SPMAK. However the adhesion (and growth) of cells to this type of copolymers was very low. Preadsorption of human plasma to pHEMA clearly stimulated the leukocyte adhesion in contrary to copolymer containing SPMAK. The extent of foreign-body reaction was significantly higher against the pHEMA compared to tested copolymer p(HEMA-co-SPMAK). In conclusion, the tested copolymer was a poorly adhesive substrate that is only poorly recognized by the non-specific immunity, although the adsorption of basic growth factors to this substrate is highly significant. Both polymers were well tolerated by the brain tissue. The phenotype of surrounding neurons was more close to the control neurons in the brain tissue surrounding the p(HEMA-co-SPMAK) implants. © 2001 Kluwer Academic Publishers     

TiO2--a prototypical memristive material

Redox-based memristive switching has been observed in many binary transition metal oxides and related compounds. Since, on the one hand, many recent reports utilize TiO(2) for their studies of the memristive phenomenon and, on the other hand, there is a long history of the electronic structure and the crystallographic structure of TiO(2) under the impact of reduction and oxidation processes, we selected this material as a prototypical material to provide deeper insight into the mechanisms behind memristive switching. In part I, we briefly outline the results of the historical and recent studies of electroforming and resistive switching of TiO(2)-based cells. We describe the (tiny) stoichiometrical range for TiO(2 - x) as a homogeneous compound, the aggregation of point defects (oxygen vacancies) into extended defects, and the formation of the various Magnéli phases. Furthermore, we discuss the driving forces for these solid-state reactions from the thermodynamical point of view. In part II, we provide new experimental details about the hierarchical transformation of TiO(2) single crystals into Magnéli phases, and vice versa, under the influence of chemical, electrical and thermal gradients, on the basis of the macroscopic and nanoscopic measurements. Those include thermogravimetry, high-temperature x-ray diffraction (XRD), high-temperature conductivity measurements, as well as low-energy electron diffraction (LEED), x-ray photoelectron spectroscopy (XPS), and LC-AFM (atomic force microscope equipped with a conducting tip) studies. Conclusions are drawn concerning the relevant parameters that need to be controlled in order to tailor the memristive properties.     

Exploring the contribution of alternative food networks to food security. A comparative analysis

Food (in)security has become a challenge not only for developing economies but also for High Income Countries. In parallel, food scholars have actively investigated the contribution of alternative food networks (AFNs) to the development of more sustainable and just food systems, paying attention to drivers, initiatives and policies supporting the development of alternatives to the dominant industrialised food system and its detrimental environmental and socio-economic impacts. However, few studies have directly addressed the contribution of AFNs to food security in the Global North. This paper aims to establish new linkages between food security debates and critical AFNs literature. For that purpose, we conduct a place-based approach to food security in a comparative analysis of initiatives of three different European contexts: Cardiff city-region (UK), the Flemish Region (Belgium) and the peri-urban area of the city of Valencia (Spain). The results unfold: i) how AFNs weave a more localised socio-economic fabric that creates new relationships between food security outcomes and specific territories, ii) hybridization processes within alternative but also conventional systems and iii) the role of advocacy and collective action at different levels. The analysis allows identification of key elements on which food security debates hinge and provides new insights to ground conceptual discussions on territorial and place-based food security approaches.