Iskanje po katalogu digitalne knjižnice

Opis: Climate change and climate-driven migration are two of the defining challenges of the twenty-first century, and there is no legal framework for protecting those displaced across national borders for climate-related reasons. The 1951 Refugee Convention hardly applies to human mobility in the context of climate change. This paper was written in the hopes of initiating a discussion concerning an alternative perspective through which persons fleeing natural disasters linked to climate change may satisfy the eligibility conditions for recognition of refugee status. Expanding the definition of refugee as defined in the Convention by including the notion of vulnerability to climate disasters that are caused by the underlying socio-economic conditions in the claimant’s home country and the role of discrimination in causing differential exposure to the climate-related disasters in legal definitions might open the door for the availability of refugee status for persons fleeing in the context of climate change. This paper proposes the adoption of a reformed human rights-based interpretation, particularly with regard to the individual nature of refugee status determination. Recalibrating the Convention to facilitate climate-induced migration could reduce political tension and social unrest in receiving countries.
Ključne besede: climate change, climate-driven migration or displacement, climate migrants, climate refugees, determination of refugee status, the 1951 refugee convention, human rights-based approach, socio-economic conditions, vulnerability to climate disasters, the role of discrimination, rights-based climate litigation
Objavljeno v DKUM: 19.04.2024; Ogledov: 168; Prenosov: 12
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Opis: The aim of this work was to develop and validate an electroanalytical method for simultaneous determination of Zn(II), Cd(II), and Pb(II) in a sample droplet with lab-on-a-chip system. Unmodified screen-printed electrodes (bare SPE using Ag/AgCl reference electrode) and Bi-film SPEs (BiFSPE) were used as electrochemical sensors. Cyclic voltammetry of [Fe(CN)6]3–/[Fe(CN)6]4– redox couple was employed for testing the reversibility of the diffusion-controlled system and square-wave anodic stripping voltammetry (SWASV) for determination of Zn(II), Cd(II), and Pb(II). SWASV was performed at deposition potential of –1.5 V vs. Ag/AgCl and deposition time of 60 s. The following validation parameters were examined: limit of detection (LOD), limit of quantification (LOQ), linearity, accuracy, and precision. LOD and LOQ for Zn(II) were both lower with BiFSPE than with bare SPE. For Cd(II), LOD and LOQ were similar for both bare SPE and BiFSPE. For Pb(II), LOD and LOQ with bare SPE could not be determined (due to intense background contribution) but were obtained with BiFSPE. Linear concentration ranges were obtained for all analytes with bare SPE and BiFSPE. Accuracy and precision were evaluated for different spiked concentrations; however, the method with bare SPE was neither accurate nor precise. With BiFSPE, the method was found to be both accurate and precise for Pb(II) at a spiked concentration of 140.0 μg/L, but not for Zn(II) or Cd(II). For the latter, problems with accuracy and precision were encountered with both bare SPE and BiFSPE. Both methods were selective for Zn(II), Cd(II), and Pb(II) determination. It can be concluded that the optimization of both methods is required for future studies.
Ključne besede: SPE, BiFSPE, heavy metals determination, SWASV, validation
Objavljeno v DKUM: 31.08.2020; Ogledov: 1211; Prenosov: 186
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Opis: This paper reports on the synthesis of a new hydroxylammonium fluoroferrate, with the formula $(NH_3OH)_3FeF_6$, obtained after dissolving iron powder in hydrofluoric acid and adding solid $NH_3OHF$. This new compound has been characterized by chemical and thermal analysis, single-crystal X-ray diffraction, and magnetic measurements. The title compound crystallizes trigonal, R3c, with cell parameters a = 11.4154(2) Å, c = 11.5720(2) Å, Z = 6. The structure consists of $NH_3OH^+$ cations and isolated $FeF_6^{3–}$ octahedra in which the central ion lies on a threefold axis. The oxygen and nitrogen atoms of the hydroxylammonium cations are donors of hydrogen bonds to fluoride anions, resulting in a network of hydrogen bonds between counterions. The effective magnetic moment $µ_{eff}$ = 5.8 BM was calculated and perfectly matches the expected value of high-spin Fe(III) ions. The thermal decomposition of the compound was studied by TG, DSC, and X-ray powder diffraction.
Ključne besede: inorganic chemistry, crystallography, coordination compounds, synthesis, crystal structure, characterization of compounds, determination of the structure of compounds, X-ray diffraction, magnetic measurements, thermal analysis, TG, DSC, hydrogen bond, metal complexes, hydroxylammonium fluoromethalatehydroxylammonium, fluoroferrate
Objavljeno v DKUM: 25.08.2017; Ogledov: 2076; Prenosov: 70
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Opis: Fifty samples of natural mineral waters from springs in Slovenia, Hungary, Germany, Czech Republic and further countries of former Yugoslavia have been analysed. The mass concentration of cations ($Na^+$, $K^+$, $Ca^{2+}$, $Mg^{2+}$, $Fe^{2+}$, $Mn^{2+}$, $NH^+_4$) and anions ($F^-$, $Cl^-$, $I^-$, $NO^-_3$, $SO_4^{2-}$, $HCO_3^-$), the spring temperature, pH, conductivity and carbon dioxide mass concentration have been measured using standard analytical methods. Appropriate statistical methods and different chemometric tools were used to evaluate the obtained data, namely, (i) descriptive statistics, (ii) principal component analysis (PCA), (iii) cluster analysis, and (iv) linear discriminant analysis (LDA). It was confirmed that Slovenian natural mineral water samples differ most from the German ones but are relatively similar to the Czech and Hungarian ones. Water samples from Hungary are similar to waters from the eastern part of Slovenia.
Ključne besede: natural mineral water, ion determination, principal component analysis, cluster analysis, linear discriminant analysis
Objavljeno v DKUM: 21.12.2015; Ogledov: 1866; Prenosov: 100
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Opis: We present an optical sensor for the detection of aqueous amines obtained by incorporating chromoionophore XV (ETHT 4001) into sol-gel thin films. Acid- and base-catalyzed sol-gel processes were studied to prepare stable ormosil layers using various amounts of organically modified sol-gel precursor such asmethyltriethoxysilane (MTriEOS). The sensor layers were coated with a protective layer of microporous white polytetrafluoroethylene (PTFE) in order to prevent interference from ions and ambient light. The measurements were carried out in a flow-through cell in the reflection mode. Acid-catalyzed ormosil layers (pH 1) based on the copolymerization of tetraethoxysilane (TEOS) and MTriEOS did not show any change in signal upon exposure to aqueous amine solutions, while base-catalyzed sensor layers (pH 3 and 13) showed significant changes in signal. The response time (t100) for the base-catalyzedsensor layer L3 (pH 13) upon exposure to different solutions containing 0-608 mmol L-1 aqueous propylamine was 20-30 s, the regeneration time was 70 s and the detection limit was 0.1 mmol L-1. The sensor response was reproducible and reversible. The porous ormosil layers permit dry sensor storage conditions.
Ključne besede: analytical chemistry, optical sensors, sol-gel technology, determination of amines, fluorimetry
Objavljeno v DKUM: 01.06.2012; Ogledov: 3256; Prenosov: 94
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