Cations In Aqueous Solution Research Articles

New thermodynamic insights into pregabalin interactions with H+, Na+, Mg2+, Ca2+, Cu2+, Zn2+: Equilibrium constants, enthalpy changes and sequestering ability

The thermodynamics of the interaction between (S)-(+)-3-aminomethyl-5-methylhexanoic acid (pregabalin) and protons was studied potentiometrically at different temperatures (288.15 ≤ T/K ≤ 310.15), ionic strengths (0.16 ≤ I/mol kg−1(H2O) ≤ 0.97, NaCl), (0.11 ≤ I/mol kg−1(H2O) ≤ 1.11, (C2H5)4NI), (0.10 ≤ I/mol kg−1(H2O) ≤ 1.03, NaClO4, only at T = 298.15 K). The protonation constants at infinite dilution and the corresponding enthalpy change values were determined, as well as their parameters for the dependence on the temperature and ionic strength. The results showed that the protonation reactions are exothermic, and that the entropic contribution is the driving force of the processes.Formation constants of pregabalin (L) with Zn2+, Cu2+, Ca2+, and Mg2+ were determined in NaCl(aq) at different ionic strength values, at 298.15 K. Different speciation models were proposed for the various metal/Pregabalin systems: ZnHL2+, ZnLOH0(aq), CuL+, CuL20(aq), CaL+, CaHL2+, and MgL+, depending on the different acid-base properties of the metals and the possible formation of sparingly soluble species. The modelling of the thermodynamic formation parameters respect to the temperature and ionic strength variation was carried out by using both the Specific Ion Interaction Theory (SIT) and an extended Debye-Hückel type equation.Being Pregabalin an emerging contaminant, it was interesting to investigate its distribution in presence of the investigated metal cations in aqueous solution simulating both biological fluid (urine) and natural water (seawater).

Inductance coil high-frequency contactless chemical sensor: Systematic study of its cationic sensitivity

Contactless sensors for chemical analysis, based on inexpensive and widely available electronic components, are a promising alternative to existing routine laboratory methods. We have proposed a novel type of a contactless sensor, composed of three simple components: an alternate current generator, an inductance coil, and a receiver. The sample, placed into the coil as a core of the inductor, modifies the current passing through the coil. Previously, we have demonstrated that this contactless sensor may have numerous applications for chemical analysis. In this work, we have explored the performance of the coil-based measuring platform further and performed the first systematic study of the response of inductance coil sensor to metal cations in aqueous solutions. Sixteen metal cations with different charge and radii were studied. Linear response ranges, sensitivity values and the comparison between univariate and multivariate regression modeling are presented. The largest linear response range was observed for transition metal cations Ni2+, Cu2+, Pb2+ and Nd3+ (10-3 – 10-1 M), the narrowest – for Li+ and Gd3+ (10-2 – 3.2x10-1 M) with R2 values larger than 0.94. The dependence of the response on the radius and the charge of the cation are discussed. The analytical characteristics of the device show its potential in contactless and low-cost chemical analysis and set the ground for the future research.

A Water-Soluble Cryptophane Decorated with Aromatic Amine Groups Shows High Affinity for Cesium and Thallium(I).

An anti-cryptophane decorated with three aromatic amine and three phenol groups shows a high affinity for the cesium and thallium cations in LiOH/H2O (0.1 M). The formation of the complexes was studied by 133Cs NMR and by 205Tl NMR spectroscopy at different temperatures. Characteristic signals for caged cesium and thallium were observed at a high field with respect to the signals of the free cations present in the bulk. Isothermal titration calorimetric experiments performed in LiOH/H2O (0.1 M) and NaOH/KCl buffer (pH = 13) allowed us to determine the parameter of complexation and to ascertain the high affinity of this cryptophane for cesium and thallium. A comparison with other cryptophanes that bind these two cations shows that the introduction of nitrogen atoms into the cryptophane backbone has an effect on the binding properties. The affinity for cesium and thallium(I) ions is in the following order of substitution: OH > NH2 > OCH2COOH. This study paves the way to the design of new efficient host molecules for the extraction of these two cations in aqueous solution.

Isotope fractionation of alkaline and alkaline-earth elements (Li, K, Rb, Mg, Ca, Sr, Ba) during diffusion in aqueous solutions

In this study, we used an improved “diffusion cell” method to precisely determine the diffusion-driven kinetic isotope fractionation factors of the Li, K, Rb, Mg, Ca, Sr, and Ba cations in aqueous solutions under room temperature. The obtained isotope fractionation factors (±2σ errors) are, α7/6Li = 0.996139 ± 0.000140, α41/39K = 0.998572 ± 0.000072, α87/85Rb = 0.999333 ± 0.000020, α26/24Mg = 0.999877 ± 0.000010, α44/42Ca = 0.999704 ± 0.000010, α88/86Sr = 0.999781 ± 0.000014, α138/135Ba = 0.999716 ± 0.000018. The results show that the charge of the cation and the ion-water bond length for the aquo ions are the two predominant factors affecting the mass dependence of isotope fractionation (β factor) during cation diffusion in aqueous solutions. Cations with higher charge numbers and shorter ion-water bond lengths exhibit less kinetic isotope fractionation during diffusion. Therefore, the isotope separation effect during diffusion (or β factor) in fluids is fundamentally controlled by the intensity of ion-water interaction. Weaker ion-water interaction (e.g., lower charge number, longer ion-water bond length) leads to less prominent hydrodynamic behavior for diffusing ions at the molecular level, thus more significant isotope fractionation in bulk solutions, and vice versa. Ions of larger radius would show stronger mass dependence of isotope fractionation (β factor), which can cancel the effect of decreasing relative isotope mass difference for heavier elements, thus kinetic isotope fractionation during diffusion in aqueous solutions remains prominent even for heavy elements such as Rb, Sr, and Ba. The diffusion-driven kinetic isotope fractionation factors measured in this study could provide a useful basis for interpreting specific natural isotopic variability of alkaline and alkaline-earth elements in supergene environments where chemical diffusion takes place.

Probing pH-Dependent Dehydration Dynamics of Mg and Ca Cations in Aqueous Solutions with Multi-Level Quantum Mechanics/Molecular Dynamics Simulations.

The dehydration of aqueous calcium and magnesium cations is the most fundamental process controlling their reactivity in chemical and biological phenomena, such as the formation of ionic solids or passing through ion channels. It holds particular relevance in light of recent advancements in the development of carbon capture techniques that rely on mineralization for long-term carbon storage. Specifically, dehydration of Ca2+ and Mg2+ is a key step in proposed carbon capture processes aiming to exploit the relatively high concentration of dissolved carbon dioxide in seawater via the formation of carbonate minerals from solvated Ca2+ and Mg2+ cations for sequestration and storage. Nevertheless, atomic-scale understanding of the dehydration of aqueous Ca2+ and Mg2+ cations remains limited. Here, we utilize rare event sampling via density functional theory molecular dynamics and embedded wavefunction theory calculations to elucidate the dehydration dynamics of aqueous Ca2+ and Mg2+. Emphasis is placed on the investigation of the effect pH has on the stability of the different coordination environments. Our results reveal significant differences in the dehydration dynamics of the two cations and provide insight into how they may be modulated by pH changes.

CO2-mineralization and carbonation reactor rig: Design and validation for in situ neutron scattering experiments-Engineering and lessons learned.

CO2 mineralization via aqueous Mg/Ca/Na-carbonate (MgCO3/CaCO3/Na2CO3) formation represents a huge opportunity for the utilization of captured CO2. However, large-scale mineralization is hindered by slow kinetics due to the highly hydrated character of the cations in aqueous solutions (Mg2+ in particular). Reaction conditions can be optimized to accelerate carbonation kinetics, for example, by the inclusion of additives that promote competitive dehydration of Mg2+ and subsequent agglomeration, nucleation, and crystallization. For tracking mineralization and these reaction steps, neutron scattering presents unprecedented advantages over traditional techniques for time-resolved in situ measurements. However, a setup providing continuous solution circulation to ensure reactant system homogeneity for industrially relevant CO2-mineralization is currently not available for use on neutron beamlines. We, therefore, undertook the design, construction, testing and implementation of such a self-contained reactor rig for use on selected neutron beamlines at the ISIS Neutron and Muon Source (Harwell, UK). The design ensured robust attachment via suspension from the covering Tomkinson flange to stabilize the reactor assembly and all fittings (~25 kg), as well as facilitating precise alignment of the entire reactor and sample (test) cell with respect to beam dimension and direction. The assembly successfully accomplished the principal tasks of providing a continuous flow of the reaction mixture (~500 mL) for homogeneity, quantitative control of CO2 flux into the mixture, and temperature and pressure regulation throughout the reaction and measurements. The design is discussed, with emphasis placed on the reactor, including its geometry, components, and all technical specifications. Descriptions of the off-beamline bench tests, safety, and functionality, as well as the installation on beamlines and trial experimental procedure, are provided, together with representative raw neutron scattering results.

Metal-binding cyclodextrins: Synthesis and complexation with Zn2+ and Ga3+ cations towards antimicrobial applications

Highly resistant bacteria producing metallo-β-lactamases (MBLs) to evade β-lactam antibiotics, constitute a major cause of life-threatening infections world-wide. MBLs exert their hydrolytic action via Zn2+ cations in their active center. Presently, there are no approved drugs to target MBLs and combat the associated antimicrobial resistance (AMR). Towards this issue, we have prepared a family of cyclodextrins substituted with iminodiacetic acid (IDA) on their narrow side, while the wider side is either unmodified or per-2,3-O-methylated. The molecules form strong coordination complexes with Zn2+ or Ga3+ cations in aqueous solution. Free and metal-complexed compounds have been thoroughly characterized regarding structures, pH-dependent ionization states, distribution of species in solution, pKa values and metal-binding constants. At neutral pH the multi-anionic hosts bind up to four Zn2+ or Ga3+ cations. In vitro, 50 μΜ of the compounds achieve complete re-sensitization of MBL-producing Gram-negative clinical bacterial strains resistant to the carbapenems imipenem and meropenem. Moreover, the radioactive complex [67Ga]Ga-β-IDACYD prepared, displays high radiochemical purity, sufficient stability both overtime and in the presence of human plasma apo-transferrin, thus providing an invaluable tool for future biodistribution and pharmacokinetic studies of β-IDACYDin vivo, prerequisites for the development of therapeutic protocols.

New insights on the picosecond time-resolved fluorescence signatures of metal cation-Morin complexes

This article is the second in the sequence of our investigations on morin and metallic cations:morin spectroscopic characterization, completing our first article centred on morin’s photophysical behavior. We explore, here, for the first time metallic cations:morin complexes with Ca(II), Zn(II) and Al(III) in MeOH by steady-state and picosecond time-resolved fluorescence techniques. We evidenced that the metallic cations:morin complexes could exhibit typical pico- and nanosecond time-resolved signatures. We observed that for the metallic cations, with the lowest complexation efficiency, we still see traces of the emission of the morin:solvent complex that we evidenced in our former article. Therefore, supported by steady-state and time-resolved spectroscopies, we present an argued assignment of the time-components extracted from the fluorescence decays to the main species present in solution. We investigated with more accuracy and sensitivity (by time-resolved fluorescence) the presence of cation in aqueous solutions than it was already performed in literature before. We hope that this work will stimulate the development of new methods for the detection of metallic cations in water including time-resolved fluorescence techniques.

Dual action of a distinctive colloidal 3-(Benzimidazole-2-yl)-2-hydroxybenzaldehyde grafted chitosan support for the continual detection ability for Hg (II) in aqueous environ and inherent emission-induced live cell imaging

In this research work, an interesting sugar based fluorescent materials has been successfully developed to detect metal ions (Hg2+) in aqueous solution. The prepared colloid, 3-(benzimidazole-2-yl)-2-hydroxy benzaldehyde/chitosan (ChI) has significant characteristics as greener and eco-friendly material. ChI has found for switching of proton transfer between enol-imine and keto-enamine forms of ChI through excited-state intramolecular proton transfer (ESIPT) mechanism. The internal chemical-bonding and functionality of ChI are confirmed through FTIR, UV–Vis, fluorescence, SEM, TEM, DLS etc. ChI shows its fluorescence-quenching, selectivity, scavenging and chelating capabilities for Hg2+ ions in the presence of other cations in aqueous solution. Spectral and XRD analysis have established the remarkable continual and consistent detection of Hg2+ in aqueous system with a limit of detection of 0.204 nM. The strong chelating agent EDTA is used to regain of fluorescence of ChI in support of labile chelation ability of ChI and to show reversibility for continual detection of Hg2+ due to the strong EDTA/Hg2+ complexation. Scavenging ability is investigated using Na2S solution followed by the XRD analysis of precipitate appeared. Also, ChI shows its efficiency for the fluorescence cell imaging in live HADF cells with negligible cytotoxicity. Convincingly, ChI has processed as materials with very significant addition and advancement for its multimodal and eco-friendly behavior in current material development research.

Combining phthalimide innate of a positive-charge nanofiltration membrane for high selectivity and rejection for bivalent cations.

A positively charged nanofiltration (NF) membrane is known to have exceptional separation performance for bivalent cations in aqueous solutions. In this study, a new NF activity layer was created using interfacial polymerization (IP) on a polysulfone (PSF) ultrafiltration substrate membrane. The aqueous phase combines the two monomers of polyethyleneimine (PEI) and phthalimide, while successfully producing a highly efficient and accurate NF membrane. The conditions of the NF membrane were studied and further optimized. The aqueous phase crosslinking process enhances the polymer interaction, resulting in an excellent pure water flux of 7.09 L·m-2·h-1·bar-1 under a pressure of 0.4 MPa. Additionally, the NF membrane shows excellent selectivity toward inorganic salts, with a rejection order of MgCl2 > CaCl2 > MgSO4 > Na2SO4 > NaCl. Under optimal conditions, the membrane was able to reject up to 94.33% of 1,000 mg/L of MgCl2 solution at an ambient temperature. Further to assess the antifouling properties of the membrane with bovine serum albumin (BSA), the flux recovery ratio (FRR) was calculated to be 81.64% after 6 h of filtration. This paper presents an efficient and straightforward approach to customize a positively charged NF membrane. We achieve this by introducing phthalimide, which enhances the membrane's stability and rejection performance.

Fast and effective sorption of radioactive Sr(II) onto mesoporous silicate

Abstract A mesoporous silicate material (MS) was effectively synthesized and applied as a solid sorbent for removal of radioactive Sr(II) ions from aqueous solution. MS was characterized using different tools including N2 adsorption-desorption analysis, FT-IR, XRD and SEM. The synthesized material has crystalline, porous nature and exhibited a large surface area of about 905.18 m2 g−1. The uptake of Sr(II) ions onto MS was investigated under different batch experimental conditions involving pH, equilibrium time, sample weight and initial concentration of Sr(II) ions. About 98 % of Sr(II) radionuclides were uptaken at pH 12 in the first minute. Different isotherm models (Langmuir, Freundlich, Dubinin-Radushkevich and Temkin) were applied to analyze the obtained experimental sorption equilibrium data. The Langmuir isotherm model was aligned well with the sorption data. The maximum sorption capacity (Q max) of MS towards strontium ions attained the value 0.991 mmol/g. The parameters (ΔG°, ΔH° and ΔS°) were calculated from thermodynamic study and their values showed that sorption process of Sr(II) ions on MS is strong, take place spontaneously, and considered as endothermic process. The synthesized MS had the ability to efficiently remove Sr(II) radionuclides even in the presence of Na+ and Ca2+ as competing cations in aqueous solution. Among the studied desorbing agents, CaCl2 was the best one for desorbing Sr(II) radionuclides loaded onto MS. The synthesized MS was reused for sorption of strontium up to four cycles with acceptable efficiency.

Comparative characteristics of the nearest environment structural parameters of metal ions in water and acetonitrile

The literature data of various research methods on the structural characteristics of the nearest environment of some monatomic inorganic cations in aqueous solutions and in acetonitrile under ambient conditions are summarized. A quantitative comparison of the cations first solvation shell structures in these solvents has been carried out. It is suggested that for these systems, the structure of solvation shells of cations do not depend on the solvent, but is determined only by the physicochemical nature of the ions.

Determination of trace amount of iron cations using electrochemical methods at N, S doped GQD modified electrode

In this work, nitrogen and sulfur co-doped graphene quantum dot-modified glassy carbon electrodes (N, S-GQD/GCE) were used for the recognition of iron cations in aqueous solutions. The dissolved cations are detected based on the faradaic reduction or oxidation current of Fe(III) and Fe(II) obtained at the N, S-GQD/GCE surface. Cyclic voltammetry (CV), square wave voltammetry (SWV), and hydrodynamic amperometry are used as suitable electrochemical techniques for studying electrochemical behavior and determination of Fe cations. Based on the obtained results, it is concluded that the presence of free electrons in the structure of N, S-GQD could facilitate electron transfer reaction between Fe(III) and electrode surface which with increased surface area results in increased sensitivity and lower limit of detection. By performing suitable experiments, the best condition for preparing the modified electrode and determining Fe(III) was selected. Under optimized conditions, the amperometric response is linear from 1 to 100 nM of Fe(III) with a detection limit of 0.23 nM. The validity of the method and applicability of the sensor is successfully tested by the determination of Fe(III) in drug and water real samples. This sensor opened a new platform based on doped nanoparticles for highly sensitive and selective detection of analytes.

Construction of Fe/N/C nano-clusters anchored on porous diatomite for efficient removal of norfloxacin via the adsorption-PMS activation

In this study, natural porous diatomite was utilized as a conciliatory carrier for the fabrication of Fe/N/C nano-clusters with assistance of binary molten salt of NaCl-ZnCl2 under different annealing temperature and used to removal of norfloxacin (NFA). The sample Fe/Dm900 (prepared at 900 °C) exhibited a high surface area and great catalytic performance for antibiotics in the presence of PMS. Over 97% NFA can be decomposed within 5 min and the final degradation rate reached 98%. Meaningfully, high-efficiency Fe/Dm900-PMS system was nearly impervious to pH values and inorganic cations in aqueous solution and could be a likely candidate for degradation of multiple contaminants in pharmaceutical outlet water. Furthermore, the other impacting variables such as catalyst dosage, PMS dosage, NFA concentration and initial pH were moreover explored towards debasement, and conceivable degradation pathways of NFA were presented through LC-MS. This work builds up a compelling procedure to synthesize super-dispersed Fe clusters, which may be amplified to other transition metal-based catalyst via molten salt.

Microhydration of the adamantane cation: intracluster proton transfer to solvent in [Ad(H2O)n=1-5]+ for n ≥ 3.

Radical cations of diamondoids are important intermediates in their functionalization reactions in polar solvents. To explore the role of the solvent at the molecular level, we characterize herein microhydrated radical cation clusters of the parent molecule of the diamondoid family, adamantane (C10H16, Ad), by infrared photodissociation (IRPD) spectroscopy of mass-selected [Ad(H2O)n=1-5]+ clusters. IRPD spectra of the cation ground electronic state recorded in the CH/OH stretch and fingerprint ranges reveal the first steps of this fundamental H-substitution reaction at the molecular level. Analysis of size-dependent frequency shifts with dispersion-corrected density functional theory calculations (B3LYP-D3/cc-pVTZ) provides detailed information about the acidity of the proton of Ad+ as a function of the degree of hydration, the structure of the hydration shell, and the strengths of the CH⋯O and OH⋯O hydrogen bonds (H-bonds) of the hydration network. For n = 1, H2O strongly activates the acidic C-H bond of Ad+ by acting as a proton acceptor in a strong CH⋯O ionic H-bond with cation-dipole configuration. For n = 2, the proton is almost equally shared between the adamantyl radical (C10H15, Ady) and the (H2O)2 dimer in a strong C⋯H⋯O ionic H-bond. For n ≥ 3, the proton is completely transferred to the H-bonded hydration network. The threshold for this size-dependent intracluster proton transfer to solvent is consistent with the proton affinities of Ady and (H2O)n and confirmed by collision-induced dissociation experiments. Comparison with other related microhydrated cations reveals that the acidity of the CH proton of Ad+ is in the range of strongly acidic phenol+ but lower than for cationic linear alkanes such as pentane+. Significantly, the presented IRPD spectra of microhydrated Ad+ provide the first spectroscopic molecular-level insight of the chemical reactivity and reaction mechanism of the important class of transient diamondoid radical cations in aqueous solution.

Lanthanide-MOFs as multi-responsive photoluminescence sensor for sensitively detecting Fe3+, Cr2O72- and nitrofuran antibiotics.

Fast and selective detection of contaminants plays a key role in meeting human health and environmental concerns. Herein, two groups of isostructural lanthanide MOFs, [Ln(Hpta)(oxalic acid)]·H2O (1-Eu, 2-Gd) and [Ln(pta)(oxalic acid)0.5(H2O)2]·2H2O (3-Eu, 4-Gd) (H2pta = 2-(4-pyridyl)-terephthalic acid, C2O4- = oxalic acid), were synthesized by solvothermal method. Single crystal X-ray diffraction reveals that 1 and 2 are 3D neutral frameworks, while 3 and 4 consist of 2D layers with parallelogram holes and stack into 3D networks through O-H⋯N and O-H⋯O hydrogen bonding interactions. All complexes remain crystalline and stable below 400 °C, suggesting preeminent thermostability. Noteworthily, only 3 shows excellent chemical stability in water and organic solvent. Therefore, the solid-state fluorescence spectrum was used to characterize 3 which exhibited intense red luminescence. The N active sites in the pore channels of 3 are conducive to displaying a distinct quenching effect for Fe3+ cations in aqueous solutions, Cr2O72- anions in DMF and DMA solutions, and nitrofuran antibiotics in the DMF solvent. Overall, 3 is a prospective luminescent sensor for detecting Fe3+, Cr2O72- and nitrofuran antibiotics.

A Chromatography–Mass Spectrometry Study of the Transformation of the Benzalkonium Cation in Aqueous Solutions under the Action of Active Bromine

A Chromatography–Mass Spectrometry Study of the Transformation of the Benzalkonium Cation in Aqueous Solutions under the Action of Active Bromine

Synthesis, Structure, and Characterization of 4,4'-(Anthracene-9,10-diylbis(ethyne-2,1-diyl))bis(1-methyl-1-pyridinium) Bismuth Iodide (C30H22N2)3Bi4I18, an Air, Water, and Thermally Stable 0D Hybrid Perovskite with High Photoluminescence Efficiency.

4,4'-(Anthracene-9,10-diylbis(ethyne-2,1-diyl))bis(1-methyl-1-pyridinium) bismuth iodide (C30H22N2)3Bi4I18 (AEPyBiI) was obtained as a black powder by a very simple route by mixing an acetone solution of BiI3 and an aqueous solution of C30H22N2I2. This novel perovskite is air and water stable and displays a remarkable thermal stability up to nearly 300 °C. The highly conjugated cation C30H22N2 2+ is hydrolytically stable, being nitrogen atoms quaternarized, and this accounts for the insensitivity of the perovskite toward water and atmospheric oxygen under ambient conditions. The cation in aqueous solution is highly fluorescent under UV irradiation (emitting yellow-orange light). AEPyBiI as well is intensely luminescent, its photoluminescence emission being more than 1 order of magnitude greater than that of high-quality InP epilayers. The crystal structure of AEPyBiI was determined using synchrotron radiation single-crystal X-ray diffraction. AEPyBiI was extensively characterized using a wide range of techniques, such as X-ray powder diffraction, diffuse reflectance UV-vis spectroscopy, Fourier transform infrared (FTIR) and Raman spectroscopies, thermogravimetry-differential thermal analysis (TG-DTA), elemental analysis, electrospray ionization mass spectroscopy (ESI-MS), and photoluminescence spectroscopy. AEPyBiI displays a zero-dimensional (0D) perovskite structure in which the inorganic part is constituted by binuclear units consisting of two face-sharing BiI6 octahedra (Bi2I9 3- units). The C30H22N2 2+ cations are stacked along the a-axis direction in a complex motif. Considering its noteworthy light-emitting properties coupled with an easy synthesis and environmental stability, and its composition that does not contain toxic lead or easily oxidable Sn(II), AEPyBiI is a promising candidate for environmentally friendly light-emitting devices.

Radiochemical quality control of the radiopharmaceutical, 89SrCl2 produced in FBTR

89SrCl2 radiopharmaceuticals is mainly used for bone pain palliation in the cancer patients, is being produced in FBTR via 89Y(n, p)89Sr using yttria target. The irradiated yttria target is chemically processed in high pure quartz distilled nitric acid medium in hot cell facility, to avoid the corrosion of components of hotcell due to chloride ions while using HCl medium. Being ionic species, the purified 89Sr(II) cation in aqueous solution containing bulk nitrate and other trace anions, exists as SrXn species where X: F−, Cl−, Br−, NO3−, PO43− and SO42−, n: stoichiometric anion content. The aim of the manuscript is to standardise an efficient ultra-low level anion purification method (ppb range) for the conversion of SrXn to SrCl2 and estimate the residual anionic impurities as recommended by the appropriate source specifications for its medical application. Various methods were standardised for the removal of anions in the SrCl2 source produced by the above process which include evaporation, calcination, anion exchange column, cation exchange column as well as its combination with pre-concentration column of ion chromatography (IC) technique using 89Sr tracers as well as FBTR produced 89Sr solution. Assay of 89Sr and other anions including nitrate for the above study were accomplished using Cerenkov counting and ion chromatography respectively. Thus evaporation-calcination-column chromatography mode was finalised to obtain pure SrCl2 source free from nitrate and other anionic impurities. This is the first ever systematic study for the Radiochemical quality control of nca 89SrCl2 radiopharmaceutical produced in a fast reactor. This study also finds its application to any analytical lab as well as industry where there is a requirement of anion purification in the ppb level.

Subnanomolar Detection of Mercury Cations in Water by an Interfacial Fluorescent Sensor Achieved by Ultrathin Film Structure Optimization.

The objectives of this work were to develop and extend the previously proposed approaches to control the structure of nanoscale planar systems based on modular fluorophore compounds capable of efficient analyte binding and to optimize the architecture of ultrathin films formed from them to create a thin-film sensor element for mercury cations. The possibility of applying the ratiometric approach to the fluorescence measurements to obtain a quantitative analytical signal was shown. It was found that films with the Langmuir-Schaefer film architecture, in which the receptor crown ether groups of the fluoroionophore are oriented toward the studied solution, allow the quantitative determination of mercury cations in water at concentrations below the threshold limit value and are especially effective in the analyte concentration range of 10-10-10-5 M. High selectivity of the obtained thin-film sensitive elements with respect to mercury cations and the possibility of regeneration of such elements after quantitative determination of mercury cations in aqueous solutions are demonstrated.