Search results for "element"
showing 10 items of 13601 documents
VIOLURATO COMPLEXES OF Cr(III). SYNTHESIS AND CHARACTERIZATION. PROTONATION-DEPROTONATION EQUILIBRIA OF THE COORDINATED LIGANDS. EVIDENCE OF THE COOR…
1982
Abstract The formation of violurato complexes of Cr(III) has been studied in aqueous solution. Two compounds, [Cr(H2V)3].5H2O and Na[Cr(H2V)2(OH)2].4H2O have been synthesized and characterized. [Cr(H2V)3] behaves in aqueous solution as a triprotic acid but it can also add a proton yielding [Cr(H2V)2(H3V)]+. The acidity constants of this species have been determined: pKa1 =3.32, pKa2 =4.25, pKa3 =4.83 and pKa4 =6.99 (25°C, 0.1 M NaC1O4). [Cr(H2V)2(OH)2]− undergoes a deprotonation of the two H2V− ligands and a protonation of the hydroxo ligands. The acidity constants of [Cr(H2V)2(H2O)2]+ have been also determined: pKa1 =3.5, pKa2 =4.6, pKa3 =7.1 and pKa4 =9.2 (25°C, 0.1 M NaC1O4). The coordin…
Structural and Vibrational Study of a New Mixed Dipotassium Hydrogenselenate Dihydrogenphosphate K2(HSeO4)1.5 (H2PO4)0.5.
2006
Abstract Ongoing studies of the KHSeO4–KH2PO4 system, aimed at developing novel proton conducting solids, resulted in the new compound K2(HSeO4)1.5(H2PO4)0.5 (dipotassium hydrogenselenate dihydrogenphosphate). The crystals have been prepared by slow evaporation of an aqueous solution at room temperature. The structural properties of the crystals were characterized by X-ray single analysis (performed at room temperature), which revealed that K2(HSeO4)1.5(H2PO4)0.5 (KHSeP) crystallizes in space group P 1 ¯ with lattice parameters: a = 7.417(3) A, b = 7.668(2) A, c = 7.744(5) A, α = 71.59(3)°, β = 87.71(4)° and γ = 86.04(6)°. The compound has a unit cell volume 416.8(3) A3 and two formula unit…
Synthesis of new molybdenum–tungsten, vanadium–tungsten and vanadium–molybdenum–tungsten oxynitrides from freeze-dried precursors
2004
Abstract Interstitial molybdenum–tungsten, vanadium–tungsten and vanadium–molybdenum–tungsten oxynitrides in the solid solution series Mo1−zWz(OxNy) and V1−zWz(OxNy) (z=0, 0.2, 0.4, 0.5, 0.6, 0.8, 1), and V1−u−zMouWz(OxNy) (u, z=0.2, 0.33, 0.4, 0.6; u+z
Synthetic routes to novel fluorogenic pyronins and silicon analogs with far-red spectral properties and enhanced aqueous stability
2020
Fluorogenic detection of reactive (bio)analytes is often achieved with "smart" probes, whose activation mechanism causes the release of aniline-based fluorophores. Indeed, the protection-deprotection of their primary amino is the simplest way to induce dramatic and valuable changes in spectral features of the fluorogenic reporter. In this context, and due to their small size and intrinsic hydrophilicity, we focused on pyronin dyes and related heteroatom analogs (i.e., formal derivatives of 3-imino-3H-xanthen-6-amine and its silicon analog) for their use as optically tunable aniline-based fluorophores. To overcome some severe limitations associated with the use of such fluorogenic scaffolds …
Zeta-Potential Study of Calcium Silicate Hydrates Interacting with Alkaline Cations
2001
An investigation into the interaction between alkaline cations and calcium silicate hydrates (CSH) was conducted by electrokinetic measurements, which provided information on the nature of the interface between the solid and its equilibrium solution. Calcium constitutes for the CSH surface a potential-determining cation. A model of the CSH surface could be proposed, accounting for the experimental evolution of the CSH zeta potential. The necessity of studying the zeta-potential evolution of the system as a function of the calcium activity, instead of its concentration, was underlined. The results obtained suggest a specific interaction between cesium and the CSH surface, whereas sodium and …
Uranium(VI) sequestration by polyacrylic and fulvic acids in aqueous solution
2011
Stability data on the formation of dioxouranium(VI) species with polyacrylic (PAA) and fulvic acids (FA) are reported with the aim to define quantitatively the sequestering capacity of these high molecular weight synthetic and naturally occurring ligands toward uranium(VI), in aqueous solution. Investigations were carried out at t = 25 °C in NaCl medium at different ionic strengths and in absence of supporting electrolyte for uranyl–fulvate (\( {{\text{UO}}_{2}}^{2+} \)–FA) and uranyl–polyacrylate (\( {{\text{UO}}_{ 2}}^{ 2+ } \)–PAA, PAA MW 2 kDa) systems, respectively. The experimental data are consistent with the following speciation models for the two systems investigated: (i) UO2(FA1),…
ChemInform Abstract: Synthesis and Magnetic Properties of Bis(μ-hydroxo)bis((2,2′-bipyridyl)copper(II)) Squarate. Crystal Structure of Bis(μ-hydroxo)…
1990
Abstract The compound [Cu2(bipy)2(OH)2](C4O4)·5.5H2O, where bipy and C4O42− correspond to 2,2′-bipyridyl and squarate (dianion of 3,4-dihydroxy-3-cyclo- butene-1,3-dione) respectively, has been synthesized. Its magnetic properties have been investigated in the 2–300 K temperature range. The ground state is a spin-triplet state, with a singlet-triplet separation of 145 cm−1. The EPR powder spectrum confirms the nature of the ground state. Well-formed single crystals of the tetrahydrate, [Cu2(bipy)2(OH)2](C4O4)·4H2O, were grown from aqueous solutions and characterized by X-ray diffraction. The system is triclinic, space group P 1 , with a = 9.022(2), b = 9.040(2), c = 8.409(2) A, α = 103.51(2…
Arsenic(III) Removal at Low Concentrations by Biosorption usingPhanerochaete chrysosporiumPellets
2013
As(III) removal from dilute aqueous solutions by biosorption onto pellets of the white rot fungus Phanerochaete chrysosporium was investigated. The As(III) uptake capacity was evaluated at low initial concentrations (0.2–1 mg/L) which revealed that the P. chrysosporium pellets were only slightly less efficient than the well studied adsorbent granular ferric hydroxide. Moreover, its performance was much more superior compared to anaerobic granular sludge, another cheaply available bacterial biosorbent. In the studied pH (5–9) and biomass concentration (0.25–1.5 g/L wet weight basis) ranges, no large differences in As(III) removal efficiency were observed. The influence of different ions, com…
Fixed‐Bed Removal of Free and Complexed Ni from Synthetic and Industrial Aqueous Solutions
2008
Abstract This paper evaluates the application of several biosorbents for Ni removal from aqueous solutions in the absence and in the presence of EDTA. Fixed bed experiments were performed (Ni influent concentration, 2 mg dm−3; EDTA doses, 0, 5, and 10 mg dm−3; pH=7) to study the process feasibility as refining after conventional physicochemical treatment. In absence of EDTA, uptake capacity followed the order peat > Posidonia oceanica > chitosan > chitin ≫ Scharlau AC. Maximum uptakes of 8.95 mg g−1 and 5.10 mg g−1 were found for peat and Posidonia oceanica, respectively. In the presence of EDTA, removal capacity decreased for all biosorbents; Ni was detected in the effluent from the beginn…
Attenuated total reflectance infrared determination of sodium nitrilotriacetate in alkaline liquid detergents
2005
Abstract An attenuated total reflectance infrared (ATR–FTIR) method has been developed for the direct determination of the chelating agent sodium nitrilotriacetate (NTA) in high pH cleaning formulations. Aqueous samples and standards were placed directly on the diamond ATR cell without any pre-treatment and FTIR spectra were recorded between 4000 and 600 cm−1. Measurement conditions were evaluated. Results obtained for five different commercial formulations containing from 6.22 to 9.25% (w/w) of NTA were in good agreement with the manufacturer's declared content (differences between 3.2 and −3.7%). Recovery studies evidenced the accuracy of the developed method, having found values between …