Search results for "Molybdate"
showing 10 items of 31 documents
In situ XAFS study of phase transitions and hydrogen intercalation in WO3-MoO3 system
1995
Abstract The WO 3 -MoO 3 system has several reconstructive and displacive phase transitions which can be induced by temperature and/or by change of stoichiometry or valence state of metal ions under hydrogen intercalation. We have studied in situ the local electronic and structural changes arising in WO 3 -MoO 3 system with hydrogen intercalation and temperature. In situ XAFS measurements at the Mo K and W L 3 edges in H y Mo x W 1− x O 3 compounds, performed at different hydrogen intercalation level and temperatures (from RT to 500°C), allowed us to determine the rearrangement in the first and second coordination shells of Mo and W cations during phase transitions. It was found that hydrog…
Cryo-negative staining
1998
Abstract A procedure is presented for the preparation of thin layers of vitrified biological suspensions in the presence of ammonium molybdate, which we termcryo-negative staining. The direct blotting of sample plus stain solution on holey carbon supports produces thin aqueous films across the holes, which are routinely thiner than the aqueous film produced by conventional negative staining on a continuous carbon layer. Because of this, a higher than usual concentration of negative stain (ca. 16% rather than 2%) is required for cryo-negative staining in order to produce an optimal image contrast. The maintenance of the hydrated state, the absence of adsorption to a carbon film and associate…
Retention of vanadium (V) by three Finnish mineral soils
1994
Summary Retention of V(V) by three Finnish mineral soils from 10−4m and 10−5m sodium vanadate solutions was investigated at room temperature in the pH range 2.3–7.5. In adsorption experiments, 0.02 m KCl was used as ionic medium, and the samples were left to equilibrate for 72 h. The solid: solution ration was 1:100 (m: v). Maximum adsorption occurred at pH ∼4, where 70–80% of the added V (350–400 μg g−1 from 10−4m solution and 35–40 μg g−1 from 10−5m solution) was retained by each soil. Retention was significant even at pH 6, where adsorption of a similar anion, molybdate, is negligible. Desorption of the retained V was measured by adding 50.0 cm3 of 0.02 M KCl into weighed soil samples an…
Modeling the acid-base properties of molybdate(VI) in different ionic media, ionic strengths and temperatures, by EDH, SIT and Pitzer equations
2017
This paper reports the results of a study on the determination of the protonation constants of MoO42 −, in NaClaq, NaNO3aq, KClaq, at different ionic strengths (0 < I/mol dm− 3 ≤ 5.0 in NaClaq, 0 < I/mol dm− 3 ≤ 3.0 in NaNO3aq and KClaq) and temperatures (278.15 ≤ T/K ≤ 318.15 in NaClaq, only 298.15 K in NaNO3aq and KClaq), by potentiometric (ISE-H+ glass electrode) and spectrophotometric (UV/Vis) titrations. After a critical analysis of results and literature findings, the proposed speciation model takes into account the formation of two monomeric and four heptameric species, namely: MoO4H−, MoO4H2, (MoO4)7H86 −, (MoO4)7H95 −, (MoO4)7H104 − and (MoO4)7H113 −. Due to the complexity of…
Spray pyrolysis synthesis and characterization of Mg1-xSrxMoO4 heterostructure with white light emission
2020
[EN] Molybdates are inorganic materials with great potential in white phosphors application, being an alternative to traditional lighting sources. In this study, we report the synthesis and characterization of Mg1-xSrxMoO4 (x = 0, 0.25, 0.50, 0.75, and 1) powders with white light-emitting properties. Using X-ray diffraction, the formation of the monoclinic beta-MgMoO4 phase was observed for x = 0 and the formation of the tetragonal scheelite phase of SrMoO4 was observed for x = 1. The formation of a heterostructure composed of both phases was found for compositions with x = 0.25, 0.50 and 0.75. Scanning and trasmission electron microscopy images showed that the Mg1-xSrxMoO4 particles exhibi…
Application of the negative staining technique to both aqueous and organic solvent solutions of polymer particles
1999
Abstract Transmission electron microscopy (TEM) imaging of several different polymers in aqueous and organic solutions using the negative staining technique is demonstrated, to emphasise the possibilities of this specimen preparation technique for polymer science. Negative stains can readily be prepared in both water and organic solvents (e.g. dimethyl formamide (DMF), dimethyl sulfoxide (DMSO) and tetrahydrofurane (THF)). Polymer particle size, size distribution and shape seen in negative stain correlates well with those of unstained materials. The particle surface and smaller particles (e.g. 10–20 nm) are more clearly defined in the presence of a negative stain. The inherent problems of s…
Propane-1,3-diammonium molybdate
2019
The reaction between equimolar amounts of propane-1,3-diamine and molybdenum trioxide in water led to the formation of single crystals of the title salt, (C3H12N2)[MoO4]. The asymmetric unit is comprised of one propane-1,3-diammonium cation and one molybdate anion. The latter is isolated in the structure and has a slightly distorted tetrahedral configuration. An extensive network of N—H...O hydrogen bonds connects anions and cations, giving rise to a compact three-dimensional packing.
Trivalent cation substitution of pulverulent cobalt—iron molybdates Co1 − xFexMoO4
1998
Abstract Different mixed cobalt—iron molybdates Co1 − xFexMoO4 (0 ≤ x ≤ 1) have been prepared by means of a ceramic process. The oxidation of pulverulent samples leads to ferric molybdate Fe2(MoO4)3, spinelle Co3O4 and cobalt molybdate CoMoO4. After a strong grinding which reduces the grain size (about 0.1 μm) and induces crystallographic defects in the grains, the cobalt—iron molybdates can be partially oxidized into cation-deficient phases. This oxidation corresponds to an isostructural substitution of part of the Fe2+ and Co2+ ions by Fe3+ and Co3+ ions and the creation of cation vacancies. The concomitant presence of trivalent cations and associated cation vacancies in the lattice stabi…
Molybdenum blue: Binding to collagen fibres and microcrystal formation
2005
Collagen fibres have been shown by transmission electron microscopy to progressively bind the polyoxomolybdate ring-complex, termed molybdenum blue. Nucleation of cuboidal molybdenum blue microcrystals occurs on the surface of the collagen fibres, leading eventually to extensive coating of the fibres with microcrystals.
Modelling the dependence on medium and ionic strength of molybdate acidbase properties, and its interactions with phytate
2016
The importance of molybdenum from a biological, environmental and technological point of view is very well known since many decades [15]. In particular, it is mainly present in aqueous solutions as molybdate (MoO42), which is the biologically active form, entering in the cells by active transport systems. Though molybdate is the major species in neutral to basic pH conditions, at lower pH it undergoes protonation and, chiefly, polymerization, even at millimolar concentration levels [2]. Consequently, the modelling of its speciation and acidbase properties is not very simple, as demonstrated by the nonhomogeneity of available literature data. In this light, our group has started a systematic…