The detection and tracking of mine-water pollution from abandoned mines using electrical tomography

Increasing emphasis is being placed on the environmental and societal impact of mining, particularly in the EU, where the environmental impacts of abandoned mine sites (spoil heaps and tailings) are now subject to the legally binding Water Framework and Mine Waste Directives. Traditional sampling to monitor the impact of mining on surface waters and groundwater is laborious, expensive and often unrepresentative. In particular, sparse and infrequent borehole sampling may fail to capture the dynamic behaviour associated with important events such as flash flooding, mine-water break-out, and subsurface acid mine drainage. Current monitoring practice is therefore failing to provide the information needed to assess the socio-economic and environmental impact of mining on vulnerable eco-systems, or to give adequate early warning to allow preventative maintenance or containment. BGS has developed a tomographic imaging system known as ALERT ( Automated time-Lapse Electrical Resistivity Tomography) which allows the near real-time measurement of geoelectric properties "on demand", thereby giving early warning of potential threats to vulnerable water systems. Permanent in-situ geoelectric measurements are used to provide surrogate indicators of hydrochemical and hydrogeological properties. The ALERT survey concept uses electrode arrays, permanently buried in shallow trenches at the surface but these arrays could equally be deployed in mine entries or shafts or underground workings. This sensor network is then interrogated from the office by wireless telemetry (e.g: GSM, low-power radio, internet, and satellite) to provide volumetric images of the subsurface at regular intervals. Once installed, no manual intervention is required; data is transmitted automatically according to a pre-programmed schedule and for specific survey parameters, both of which may be varied remotely as conditions change (i.e: an adaptive sampling approach). The entire process from data capture to visualisation on the web-portal is seamless, with no manual intervention. Examples are given where ALERT has been installed and used to remotely monitor (i) seawater intrusion in a coastal aquifer (ii) domestic landfills and contaminated land and (iii) vulnerable earth embankments. The full potential of the ALERT concept for monitoring mine-waste has yet to be demonstrated. However we have used manual electrical tomography surveys to characterise mine-waste pollution at an abandoned metalliferous mine in the Central Wales orefield in the UK. Hydrogeochemical sampling confirms that electrical tomography can provide a reliable surrogate for the mapping and long-term monitoring of mine-water pollution

Hydrogen absorption properties of amorphous (Ni0.6Nb0.4−yTay)100−xZrx membranes

Ni based amorphous materials have great potential as hydrogen purification membranes. In the present work the melt spun (Ni0.6Nb0.4−yTay)100−xZrx with y=0, 0.1 and x=20, 30 was studied. The result of X-ray diffraction spectra of the ribbons showed an amorphous nature of the alloys. Heating these ribbons below T < 400 °C, even in a hydrogen atmosphere (1−10 bar), the amorphous structure was retained. The crystallization process was characterized by differential thermal analysis and the activation energy of such process was obtained. The hydrogen absorption properties of the samples in their amorphous state were studied by the volumetric method, and the results showed that the addition of Ta did not significantly influence the absorption properties, a clear change of the hydrogen solubility was observed with the variation of the Zr content. The values of the hydrogenation enthalpy changed from ~37 kJ/mol for x=30 to ~9 kJ/mol for x=20. The analysis of the volumetric data provides the indications about the hydrogen occupation sites during hydrogenation, suggesting that at the beginning of the absorption process the deepest energy levels are occupied, while only shallower energy levels are available at higher hydrogen content, with the available interstitial sites forming a continuum of energy levels

Stress response to cadmium and manganese in Paracentrotus lividus developing embryos is mediated by nitric oxide

Increasing concentrations of contaminants, often resulting from anthropogenic activities, have been reported to occur in the marine environment and affect marine organisms. Among these, the metal ions cadmium and manganese have been shown to induce developmental delay and abnormalities, mainly reflecting skeleton elongation perturbation, in the sea urchin Paracentrotus lividus, an established model for toxicological studies. Here, we provide evidence that the physiological messenger nitric oxide (NO), formed by l-arginine oxidation by NO synthase (NOS), mediates the stress response induced by cadmium and manganese in sea urchins. When NO levels were lowered by inhibiting NOS, the proportion of abnormal plutei increased. Quantitative expression of a panel of 19 genes involved in stress response, skeletogenesis, detoxification and multidrug efflux processes was followed at different developmental stages and under different conditions: metals alone, metals in the presence of NOS inhibitor, NO donor and NOS inhibitor alone. These data allowed the identification of different classes of genes whose metal-induced transcriptional expression was directly or indirectly mediated by NO. These results open new perspectives on the role of NO as a sensor of different stress agents in sea urchin developing embryos. © 2014 Elsevier B.V

Variable phenotype in 17q12 microdeletions: Clinical and molecular characterization of a new case

Microdeletions of 17q12 including the hepatocyte nuclear factor 1 beta (HNF1B) gene, as well as point mutations of this gene, are associated with the Renal Cysts and Diabetes syndrome (RCAD, OMIM 137920) and genitourinary alterations. Also, microdeletions encompassing HNF1B were identified as a cause of Mayer\u2013Rokitansky\u2013 K\ufcster\u2013Hauser Syndrome (MRKH, OMIM277000) in females and, recently,were associatedwith intellectual disability, autistic features, cerebral anomaly and facial dysmorphisms. In this report, we describe a boywith a deletion in 17q12 region detected by SNP array, encompassing the HNF1B gene, that showed dysmorphic features, intellectual disability (ID), serious speech delay and autistic features. In addition, obesity was observed. In order to study the parental origin of the rearrangement, we analyzed selected SNPs in the deleted area in the patient and his parents, showing Mendelian incompatibilities suggesting a de novo deletion on the chromosome of maternal origin. Our case confirms the incomplete penetrance and variable expressivity of this deletion, its complex clinical variability, and strengthens the evidence that ID and stereotyped behaviors may be part of the phenotypic spectrum characterizing the affected patients. Also, it is useful to further delineate the phenotypes associated to the deletion being the first case in which obesity has been documented. We present a genotype\u2013phenotype correlation discussing the possible role of some genes, encompassed by the deletion, in the etiology of the observed phenotypes

Some Considerations about the Anodic Limit of Ionic Liquids Obtained by Means of DFT Calculations

Ionic liquids are good candidates as the main component of safe electrolytes for high-energy lithium-ion batteries. The identification of a reliable algorithm to estimate the electrochemical stability of ionic liquids can greatly speed up the discovery of suitable anions able to sustain high potentials. In this work, we critically assess the linear dependence of the anodic limit from the HOMO level of 27 anions, whose performances have been experimentally investigated in the previous literature. A limited r Pearson’s value of ≈0.7 is found even with the most computationally demanding DFT functionals. A different model considering vertical transitions in a vacuum between the charged state and the neutral molecule is also exploited. In this case, the best-performing functional (M08-HX) provides a Mean Squared Error (MSE) of 1.61 V2 on the 27 anions here considered. The ions which give the largest deviations are those with a large value of the solvation energy, and therefore, an empirical model that linearly combines the anodic limit calculated by vertical transitions in a vacuum and in a medium with a weight dependent on the solvation energy is proposed for the first time. This empirical method can decrease the MSE to 1.29 V2 but still provides an r Pearson’s value of ≈0.72

Molecular assembling in mixtures of hydrophilic 1-butyl-1-methylpyrrolidinium dicyanamide ionic liquid and water

The infrared absorbance spectrum of the ionic liquid 1-butyl-1-methylpyrrolidinium dicyanamide, mixed with water at two different concentrations, was measured between 160 and 300 K in the mid infrared range. Both mixtures do not crystallize on cooling; however, remarkably, the one with an ionic liquid (IL):water composition of 1:3 displays a cold crystallization process on heating in a restricted temperature range between 240 and 250 K. A portion of the water participates to the cold crystallization. On the contrary, with an IL:water composition of 1:6.6 no crystallization takes place. Upon water addition the vibration frequencies of the anion and of some lines of the cation are blue shifted, while the absorption lines of water are red shifted. These facts are interpreted as the evidence of the occurrence of the hydrogen bonding of water, as the hydrogen bonding acceptor with respect to the anion (anion···O-H bonds develop) and as hydrogen donor for the cation (C-H···O bonds can form). Microscopic inhomogeneities in the samples and their evolution with temperature are discussed

Low Frequency Mechanical Spectroscopy Study of Three Pyrrolidinium Based Ionic Liquids

Abstract In this work we present our recent results on three ionic liquids (ILs), which share bis(trifluoromethanesulfonyl)imide (TFSI) as anion and have different pyrrolidinium based cations. By means of a combination of mechanical spectroscopy and thermal analysis, many of the physical processes occurring during cooling down from the liquid phase, can be studied. Depending both on the diverse cation and the different thermal history, crystallization from the melt or glass transition, cold-crystallization, solid-solid phase transitions and thermally activated processes are observed. In one of the ILs, which could be easily undercooled, a prominent thermally activated peak could be observed above the glass transition. The temperature dependence of the relaxation time is approximated by a Vogel-Fulcher-Tamman equation, as usual for fragile glass forming liquids, and the apparent activation energy of W = 0.36 eV with a pre-exponential factor of the relaxation time τ0 = 1.7 · 10−13s were derived supposing jumps between asymmetrical potential wells. The kinetics of the crystallization processes have been studied in the framework of the Johnson-Mehl-Avrami-Kolmogorov theory and the Avrami parameters have been derived for both the crystallization from the melt and for the cold crystallization observed on heating

Dynamics of Mn3+ in off-stoichiometric LiMn1.5Ni0.5O4

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Temperature and pressure dependence of the infrared spectrum of 1-ethyl-3-methylimidazolium trifluoromethanesulfonate ionic liquid

The infrared absorption spectrumof 1-ethyl-3-methylimidazoliumtrifluoromethanesulfonate (EMI-TfO) was investigated at ambient pressure and variable temperatures between 120 and 330 K, or at roomtemperature and variable pressures up to 10 GPa. Upon cooling, the ionic liquid crystallizes; on the contrary, upon compression no evidence of crystallization can be obtained from the infrared spectra. Moreover, Density Functional Theory (DFT) calculations were applied to gain a better description of the ionic couple. The !B97X-D functional, including not only the empirical dispersion corrections but also the presence of a polar solvent, gives a good agreement with the infrared spectrum and suggests that TfO resides above the plane of the imidazolium, with the shorter distance between the O atom of the anion and the C2 atom of the imidazolium ring equal to 2.23 A