Sr Salts Research Articles

Mechanical properties of simulated dentin caries treated with metal cations and L-ascorbic acid 2-phosphate.

This pH cycling study aimed to investigate the effects of L-Ascorbic acid 2-phosphate (AA2P) salts of Mg, Zn, Mn, Sr, and Ba on the surface microhardness, compressive strength, diametral tensile strength (DTS), and solubility of root canal dentin. 186 cylindrical dentin specimens from 93 teeth were fortified with optimal concentrations of AA2P salts of Mg (0.18mM), Zn (5.3µM), Mn (2.2 × 10-8M), Sr (1.8µM), and Ba (1.9µM). Saline was used as the control group. These dentin specimens underwent a 3-day cycling process simulating dentin caries formation through repeated sequences of demineralization and remineralization. Surface microhardness at 100 and 500µm depths (n = 10/subgroup), scanning electron microscopy (n = 3/group), compressive strength (n = 10/group), DTS (n = 6/group), and solubility (n = 5/group) tests were performed to analyze the dentin specimens. Data were analyzed using Kolmogorov-Smirnov, one-way ANOVA, and Post Hoc Tukey tests (p < 0.05). The control group had significantly lower microhardness at both depths (p < 0.001), reduced DTS (p = 0.001), decreased compressive strength (p < 0.001), and higher weight loss (p < 0.001) than all other groups. The Sr group had the highest compressive strength and microhardness among all the groups. The microhardness was significantly higher for the 500µm depth than the 100µm depth (p < 0.001), but the difference in microhardness between depths across groups was not significant (p = 0.211). All fortifying solutions provided some protection against artificial caries lesions. Therefore, these elements might have penetrated and reinforced the demineralized dentin against acid dissolution.

Comparison of the dosimetric response of two Sr salts irradiated with 60Co γ-rays and synchrotron X-rays at ultra-high dose rate

As part of the development of innovative radiotherapy techniques using X-ray synchrotron sources, namely FLASH-radiotherapy and microbeam radiation therapy (MRT), two rod dosimeters based on strontium sulfate (SrSO4) and strontium carbonate (SrCO3) were developed and irradiated at the ESRF-ID17 Biomedical beamline to investigate new solid-state dosimeters.The radiation-induced defect in Sr-based dosimeters was detected by means of an electron paramagnetic resonance (EPR) spectrometer. For the study, the EPR response of the dosimeters irradiated with synchrotron X-rays in the 30–600 keV range and dose rate of 11.6 kGy/s was compared with the response after irradiation with a 60Co γ-ray source with a dose rate of 0.288 Gy/s.Both Sr dosimeters show an increased intensity of the EPR signal in the case of irradiation at the synchrotron with respect to the case of 60Co γ-ray irradiation. The measured enhancement of the delivered dose is explained by the fact that Sr shows an increased photoelectric interaction at orthovoltage X-ray energies, producing an increased number of free radicals.The experimental relative response rESRF of the EPR signals between samples irradiated at the ID17 beamline and the 60Co beam quality was found to be 9.66 for SrSO4 and 11.19 for SrCO3. Meanwhile, the theoritical relative responses rμen/ρESRF calculated as the ratio of mass energy absorption coefficients (μen/ρ) of the dosimeters to that for water at the ID17 with respect to the 60Co beam was found to be 11.85 for SrSO4 and 13.31 for SrCO3.The increased EPR response of Sr salt dosimeters irradiated with photons in the keV range proved that these detectors type could be a good candidate for the development of very sensible detectors for radiotherapy applications.

Effects of Sterilization and Hydrolytic Degradation on the Structure, Morphology and Compressive Strength of Polylactide-Hydroxyapatite Composites.

Composites based on polylactide (PLA) and hydroxyapatite (HA) were prepared using a thermally induced phase separation method. In the experimental design, the PLA with low weight-average molar mass (Mw) and high Mw were tested with the inclusion of HA synthesized as whiskers or hexagonal rods. In addition, the structure of HA whiskers was doped with Zn, whereas hexagonal rods were mixed with Sr salt. The composites were sterilized and then incubated in phosphate-buffered saline for 12 weeks at 37 °C, followed by characterization of pore size distribution, molecular properties, density and mechanical strength. Results showed a substantial reduction of PLA Mw for both polymers due to the preparation of composites, their sterilization and incubation. The distribution of pore size effectively increased after the degradation process, whereas the sterilization, furthermore, had an impact on pore size distribution depending on HA added. The inclusion of HA reduced to some extent the degradation of PLA quantitatively in the weight loss in vitro compared to the control without HA. All produced materials showed no cytotoxicity when validated against L929 mouse skin fibroblasts and hFOB 1.19 human osteoblasts. The lack of cytotoxicity was accompanied by the immunocompatibility with human monocytic cells that were able to detect pyrogenic contaminants.

Disulfonated azo dyes: metal coordination and ion-pair separation in twelve MII compounds of Ponceau Xylidine and Crystal Scarlet.

The structures of seven divalent metal cation compounds of Ponceau Xylidine {PX; systematic name of dication: 4-[2-(3,4-dimethylphenyl)hydrazin-1-ylidene]-3-oxo-3,4-dihydronaphthalene-2,7-disulfonate}, also known as Acid Red 26, CI 16150, and of five divalent metal cation compounds of Crystal Scarlet {CS; systematic name of dication: 8-[2-(naphthalen-1-yl)hydrazin-1-ylidene]-7-oxo-7,8-dihydronaphthalene-1,3-disulfonate}, also known as Acid Red 44, CI 16250, are presented. These are hexaaquamagnesium(II) PX dimethylformamide (DMF) monosolvate, [Mg(H2O)6](C18H14N2O7S2)·C3H7NO, (I); heptaaquacalcium(II) PX 2.5-hydrate, [Ca(H2O)7](C18H14N2O7S2)·2.5H2O, (II); catena-poly[aqua(μ-DMF)tris(DMF)bis(μ3-PX)distrontium(II)], [Sr(C18H14N2O7S2)(C3H7NO)2(H2O)0.5]n, (III); the transition-metal series hexaaquametal(II) PX DMF monosolvate, [M(H2O)6](C18H14N2O7S2)·C3H7NO, where M (metal) = Co, (IV), Ni, (V), Cu, (VI), and Zn, (VII); heptaaquacalcium(II) CS monohydrate, [Ca(H2O)7](C20H13N2O7S2)·H2O, (VIII); octaaquastrontium(II) CS monohydrate, [Sr(H2O)8](C20H13N2O7S2)·H2O, (IX); catena-poly[[triaqua(DMF)barium(II)]-μ-CS], [Ba(C20H13N2O7S2)(C3H7NO)(H2O)3]n, (X); tetrakis(DMF)(CS)copper(II) monohydrate, [Cu(C20H13N2O7S2)(C3H7NO)4]·H2O, (XI); and catena-poly[[[aquatris(DMF)zinc(III)]-μ-CS] diethyl ether hemisolvate], {[Zn(C20H13N2O7S2)(C3H7NO)3(H2O)]·0.5C4H10O}n, (XII). In all cases, the structures obtained were solvates with dimethylformamide (DMF) and/or water present. The disulfonated naphthalene-based azo anions adopt hydrazone tautomeric forms. The structures of the Mg salt and of four transition-metal forms (M = Co, Ni, Cu and Zn) of PX are found to form an isostructural series. All have solvent-separated ion-pair (SSIP) type structures and the formula [M(H2O)6][PX]·DMF. The Ca salt of PX also has an SSIP structure, but has a higher hydration state, [Ca(H2O)7][PX]·2.5H2O. In contrast, the Sr salt of PX, [Sr(PX)(DMF)2(H2O)0.5]n forms a one-dimensional coordination polymer. Both the Ca and the Sr salt of CS have an SSIP structure, namely [Ca(H2O)7][CS]·H2O and [Sr(H2O)8][CS]·H2O, whilst the heavier Ba analogue, [Ba(CS)(DMF)(H2O)3]n, forms a one-dimensional coordination polymer. Unlike PX, two CS structures containing transition metals are found to be coordination complexes, [Cu(CS)(DMF)4]·H2O and {[Zn(CS)(DMF)3(H2O)]·0.5Et2O}n. This suggests that CS is a better ligand than PX for transition metals. The Cu complex forms discrete molecules with Cu in a square-pyramidal environment, whilst the Zn species is a one-dimensional coordination polymer based on octahedral Zn centres.

Bioactive Sr(II)/Chitosan/Poly(ε-caprolactone) Scaffolds for Craniofacial Tissue Regeneration. In Vitro and In Vivo Behavior.

In craniofacial tissue regeneration, the current gold standard treatment is autologous bone grafting, however, it presents some disadvantages. Although new alternatives have emerged there is still an urgent demand of biodegradable scaffolds to act as extracellular matrix in the regeneration process. A potentially useful element in bone regeneration is strontium. It is known to promote stimulation of osteoblasts while inhibiting osteoclasts resorption, leading to neoformed bone. The present paper reports the preparation and characterization of strontium (Sr) containing hybrid scaffolds formed by a matrix of ionically cross-linked chitosan and microparticles of poly(ε-caprolactone) (PCL). These scaffolds of relatively facile fabrication were seeded with osteoblast-like cells (MG-63) and human bone marrow mesenchymal stem cells (hBMSCs) for application in craniofacial tissue regeneration. Membrane scaffolds were prepared using chitosan:PCL ratios of 1:2 and 1:1 and 5 wt % Sr salts. Characterization was performed addressing physico-chemical properties, swelling behavior, in vitro biological performance and in vivo biocompatibility. Overall, the composition, microstructure and swelling degree (≈245%) of scaffolds combine with the adequate dimensional stability, lack of toxicity, osteogenic activity in MG-63 cells and hBMSCs, along with the in vivo biocompatibility in rats allow considering this system as a promising biomaterial for the treatment of craniofacial tissue regeneration.

One unprecedented 3-D strontium–organic framework constructed from 2-(3,4-methylenedioxyphenyl)-imidazole dicarboxylate and water ligands

Hydrothermal reaction of Sr(II) salt with the promising multifunctional organic ligand, 2-(3,4-methylenedioxyphenyl)-1 H -imidazole-4,5-dicarboxylic acid (MDPhH 3 IDC), leads to one new Sr(II) polymer, namely [Sr(MDPhH 2 IDC) 2 (H 2 O) 3 ] n ( 1 ), which has been structurally characterized by elemental analysis, IR spectrum, and single crystal X-ray diffraction analysis. In polymer 1 , the Sr(II) atoms are linked by water ligands to develop many 1-D chains. These chains are further joined by the MDPhH 2 IDC − ligands to build up a fascinating 3-D structure. Interestingly, the polymer contains many dinuclear Sr(II) clusters as secondary building blocks. The thermal and photoluminescence properties of the polymer have been investigated as well. One Sr(II) polymer has been successfully isolated from the reaction of 2-(3,4-methylenedioxyphenyl)-1 H -imidazole-4,5-dicarboxylic acid (MDPhH 3 IDC) with equal amount of Sr(II) salt under hydrothermal condition. It has been structurally characterized by elemental analysis, IR spectroscopy and single-crystal X-ray diffraction. • One 3D Sr polymer has been isolated. • 3,4-methylenedioxyphenyl imidazole dicarboxylate hydrothermally reacts with Sr ion. • The polymer has structurally characterized. • The thermal and photoluminescence properties of the polymer have been determined.

Alkaline earth metal salts of 1-naphthoic acid

The structures of the Mg, Ca, Sr and Ba salts of 1-naphthoic acid are examined and compared with analogous structures of salts of benzoate derivatives. It is shown that catena-poly[[[diaquabis(1-naphthoato-κO)magnesium(II)]-μ-aqua] dihydrate], {[Mg(C(11)H(7)O(2))(2)(H(2)O)(3)]·2H(2)O}(n), exists as a one-dimensional coordination polymer that propagates only through Mg-OH(2)-Mg interactions along the crystallographic b direction. In contrast with related benzoate salts, the naphthalene systems are large enough to prevent inorganic chain-to-chain interactions, and thus species with inorganic channels rather than layers are formed. The Ca, Sr and Ba salts all have metal centres that lie on a twofold axis (Z' = 1/2) and all have the common name catena-poly[[diaquametal(II)]-bis(μ-1-naphthoato)-κ(3)O,O':O;κ(3)O:O,O'], [M(C(11)H(7)O(2))(2)(H(2)O)(2)](n), where M = Ca, Sr or Ba. The Ca and Sr salts are essentially isostructural, and all three species form one-dimensional coordination polymers through a carboxylate group that forms three M-O bonds. The polymeric chains propagate via c-glide planes and through MOMO four-membered rings. Again, inorganic channel structures are formed rather than layered structures, and the three structures are similar to those found for Ca and Sr salicylates and other substituted benzoates.

Crystallization of a Keplerate-type polyoxometalate into a superposed kagome-lattice with huge channels

Crystal structures of two Sr(2+) salts of the Keplerate-type polyoxometalate, [Mo(VI)(72)Mo(V)(60)O(372)(CH(3)COO)(30)(H(2)O)(72)](42-), have been determined by single crystal X-ray diffraction. One compound exhibits a superposed kagome-lattice with huge channels whose diameters measure approximately 3.0 nm, while the arrangement of the Keplerate anions in the other compound approximates to a distorted cubic close packing.

Nanoporous Carbohydrate Metal–Organic Frameworks

The binding of alkali and alkaline earth metal cations by macrocyclic and diazamacrobicyclic polyethers, composed of ordered arrays of hard oxygen (and nitrogen) donor atoms, underpinned the development of host-guest supramolecular chemistry in the 1970s and 1980s. The arrangement of -OCCO- and -OCCN- chelating units in these preorganized receptors, including, but not limited to, crown ethers and cryptands, is responsible for the very high binding constants observed for their complexes with Group IA and IIA cations. The cyclodextrins (CDs), cyclic oligosaccharides derived microbiologically from starch, also display this -OCCO- bidentate motif on both their primary and secondary faces. The self-assembly, in aqueous alcohol, of infinite networks of extended structures, which have been termed CD-MOFs, wherein γ-cyclodextrin (γ-CD) is linked by coordination to Group IA and IIA metal cations to form metal-organic frameworks (MOFs), is reported. CD-MOF-1 and CD-MOF-2, prepared on the gram-scale from KOH and RbOH, respectively, form body-centered cubic arrangements of (γ-CD)(6) cubes linked by eight-coordinate alkali metal cations. These cubic CD-MOFs are (i) stable to the removal of solvents, (ii) permanently porous, with surface areas of ~1200 m(2) g(-1), and (iii) capable of storing gases and small molecules within their pores. The fact that the -OCCO- moieties of γ-CD are not prearranged in a manner conducive to encapsulating single metal cations has led to our isolating other infinite frameworks, with different topologies, from salts of Na(+), Cs(+), and Sr(2+). This lack of preorganization is expressed emphatically in the case of Cs(+), where two polymorphs assemble under identical conditions. CD-MOF-3 has the cubic topology observed for CD-MOFs 1 and 2, while CD-MOF-4 displays a channel structure wherein γ-CD tori are perfectly stacked in one dimension in a manner reminiscent of the structures of some γ-CD solvates, but with added crystal stability imparted by metal-ion coordination. These new MOFs demonstrate that the CDs can indeed function as ligands for alkali and alkaline earth metal cations in a manner similar to that found with crown ethers. These inexpensive, green, nanoporous materials exhibit absorption properties which make them realistic candidates for commercial development, not least of all because edible derivatives, fit for human consumption, can be prepared entirely from food-grade ingredients.

Determination of sorption capacity of fucoidic sands for Cs+ and Sr2+ under dynamic column conditions

In this paper, the sorption behavior of Cs+ and Sr2+ on column of fucoidic sands under dynamic flow conditions was investigated, and their sorption capacities (SC) towards these two cations were studied. The determination of SC is based on the construction of respective breakthrough curves using 137Cs and 85Sr radionuclides as isotopic indicators in laboratory experiments. The samples were taken from several parts of the borehole in the area of interest. Undisturbed cores of 5 cm in diameter and 10 cm long were put in the glass columns and the cores were perfectly tightened using acrylate resin. In this time-dependence study, the so-called cenoman background groundwater was used. A concentration of 10−6 mol/dm3 of Cs+ and Sr2+ in liquid phase individually was established using neutral salts of CsNO3 and Sr(NO3)2, respectively. The groundwater was introduced at the bottom of the columns by a multi-head peristaltic pump, at a constant flow-rate of about 4 cm3/h. The results show that the sorption capacity of the investigated fucoidic sands for 137Cs and 85Sr is 0.1–1.5 and 0.05–0.5 μmol/100 g, respectively, in dependence on the evaluation of corresponding breakthrough curves. Some differences in the behavior of the cores during the experiments have also been observed and explained.

Magnetic and Cytotoxicity Properties of La1−xSr x MnO3(0 ≤ x ≤ 0.5) Nanoparticles Prepared by a Simple Thermal Hydro-Decomposition

This study reports the magnetic and cytotoxicity properties of magnetic nanoparticles of La1−xSrxMnO3(LSMO) withx = 0, 0.1, 0.2, 0.3, 0.4, and 0.5 by a simple thermal decomposition method by using acetate salts of La, Sr, and Mn as starting materials in aqueous solution. To obtain the LSMO nanoparticles, thermal decomposition of the precursor was carried out at the temperatures of 600, 700, 800, and 900 °C for 6 h. The synthesized LSMO nanoparticles were characterized by XRD, FT-IR, TEM, and SEM. Structural characterization shows that the prepared particles consist of two phases of LaMnO3(LMO) and LSMO with crystallite sizes ranging from 20 nm to 87 nm. All the prepared samples have a perovskite structure with transformation from cubic to rhombohedral at thermal decomposition temperature higher than 900 °C in LSMO samples ofx ≤ 0.3. Basic magnetic characteristics such as saturated magnetization (MS) and coercive field (HC) were evaluated by vibrating sample magnetometry at room temperature (20 °C). The samples show paramagnetic behavior for all the samples withx = 0 or LMO, and a superparamagnetic behavior for the other samples havingMSvalues of ~20–47 emu/g and theHCvalues of ~10–40 Oe, depending on the crystallite size and thermal decomposition temperature. Cytotoxicity of the synthesized LSMO nanoparticles was also evaluated with NIH 3T3 cells and the result shows that the synthesized nanoparticles were not toxic to the cells as determined from cell viability in response to the liquid extract of LSMO nanoparticles.

Minerals and vitamins in bone health: the potential value of dietary enhancement

Nutrition is important to bone health, and a number of minerals and vitamins have been identified as playing a potential role in the prevention of bone diseases, particularly osteoporosis. Despite this, there is currently no consensus on maximum levels to allow in food or as dietary supplements. The benefits of supplementation of populations at risk of osteoporosis with Ca and vitamin D are well established. Prolonged supplementation of Ca and vitamin D in elderly has been shown to prevent bone loss, and in some intervention studies to prevent fragility fractures. Although P is essential to bone health, the average intake is considered to be more than sufficient and supplementation could raise intake to adverse levels. The role of vitamin K in bone health is less well defined, though it may enhance the actions of Ca and vitamin D. Sr administered in pharmacological doses as the ranelate salt was shown to prevent fragility fractures in postmenopausal osteoporosis. However, there is no hard evidence that supplementation with Sr salts would be beneficial in the general population. Mg is a nutrient implicated in bone quality, but the benefit of supplementation via foodstuffs remains to be established. A consensus on dietary supplementation for bone health should balance the risks, for example, exposure of vulnerable populations to values close to maximal tolerated doses, against evidence for benefits from randomised clinical trials, such as those for Ca and vitamin D. Feedback from community studies should direct further investigations and help formulate a consensus on dietary supplementation for bone health.

A simple thermal decomposition synthesis, magnetic properties, and cytotoxicity of La0.7Sr0.3MnO3 nanoparticles

This study reports the new and simple synthesis of magnetic La0.7Sr0.3MnO3 (LSMO) nanoparticles by thermal decomposition method using acetate salts of La, Sr and Mn as starting materials. To obtain the LSMO nanoparticles, thermal decomposition of the precursor is carried out at the temperatures of 600, 700, 800, 900, and 1000°C for 6 hours. The synthesized LSMO nanoparticles were characterized by XRD, FT-IR, TEM and SEM. Structural characterization shows that the prepared particles consisted of two phases of LaMnO3 (LMO) and LSMO with crystallite sizes ranging from 18 to 55 nm. All the prepared samples have a perovskite structure which changes from cubic to rhombohedral with the increase in the thermal decomposition temperature. Basic magnetic characteristics such as saturation magnetization (M S) and coercive field (H C) are evaluated by sample vibrating magnetometry at room temperature (20°C). The samples show soft ferromagnetic behavior with M S values of ∼9–55 emu/g and H C values of ∼8–37 Oe, depending on the crystallite size and thermal decomposition temperature. The relationship between the crystallite size and the magnetic properties is presented and discussed. The cytotoxicity of synthesized LSMO nanoparticles was also evaluated with NIH 3T3 cells and the result showed that the synthesized nanoparticles were not toxic to the cells as determined from cell viability in response to the liquid extraction of LSMO nanoparticles.

Production of thermostable invertases by Aspergillus caespitosus under submerged or solid state fermentation using agroindustrial residues as carbon source.

The filamentous fungus Aspergillus caespitosus was a good producer of intracellular and extracellular invertases under submerged (SbmF) or solid-state fermentation (SSF), using agroindustrial residues, such as wheat bran, as carbon source. The production of extracellular enzyme under SSF at 30°C, for 72h, was enhanced using SR salt solution (1:1, w/v) to humidify the substrate. The extracellular activity under SSF using wheat bran was around 5.5-fold higher than that obtained in SbmF (Khanna medium) with the same carbon source. However, the production of enzyme with wheat bran plus oat meal was 2.2-fold higher than wheat bran isolated. The enzymatic production was affected by supplementation with nitrogen and phosphate sources. The addition of glucose in SbmF and SSF promoted the decreasing of extracellular activity, but the intracellular form obtained in SbmF was enhanced 3-5-fold. The invertase produced in SSF exhibited optimum temperature at 50°C while the extra- and intracellular enzymes produced in SbmF exhibited maximal activities at 60°C. All enzymatic forms exhibited maximal activities at pH 4.0-6.0 and were stable up to 1 hour at 50°C.

Geopolymerisation kinetics. 3. Effects of Cs and Sr salts

Alternating current impedance spectroscopy (ACIS) is used to monitor in situ the kinetics of geopolymer formation by alkali silicate activation of metakaolin at 40 °C. The evolution of conductivity and resistivity as a function of time are found to correlate very well with existing models of geopolymerisation kinetics. The dissolution of metakaolin gives a rapid increase in conductivity, with a subsequent decrease due to gelation and gel ageing. After a period of curing, the resistivity of the gel network is seen to be a sensitive probe of the development of a well-formed gel structure. This enables investigation of the changes in geopolymer formation kinetics and gel structure caused by addition of various salts of interest in nuclear waste management, in particular the nitrate, sulphate and hydroxide salts of caesium and strontium. Each of the six salts studied is shown to have specific effects on the kinetics of geopolymer formation and the pore structure of the final geopolymer gel. Caesium nitrate and caesium sulphate have very similar effects, with a slight retardation of gelation followed by significant disruption of gel structure while caesium hydroxide accelerates gel formation markedly. Strontium nitrate at high concentrations interferes significantly with the pore network development, while strontium sulphate is converted gradually to carbonate salts by atmospheric carbonation.

Environmental and technical considerations of preflux bath composition on structure of hot dip zinc galvanised coatings

The influence of the preflux bath composition upon the structure of zinc coatings deposited with hot dip galvanising has been examined. Various compositions were studied containing chloride salts of Na, K and Sr. The as formed coatings were examined by optical microscopy, scanning electron microscopy and X-ray diffraction. Depending on each specific compound and its concentration in the preflux bath, different crystallisation procedures are induced, which finally results in the formation of Fe–Zn intermetallic phases with different morphologies, thicknesses and qualities. Fluxing in an aqueous solution of NaCl or KCl introduced several cracks in and between the phases while fluxing in an aqueous solution of SrCl2 caused total failure of the coating because it had no cohesion to the substrate. However, when the same salts were dissolved in an aqueous solution containing 50 wt-%ZnCl2·2NH4Cl instead of water, the coatings were improved.

Characterization of LSM-YSZ Composites Prepared by Impregnation Methods

Composites of (LSM) and yttria-stabilized zirconia (YSZ) were prepared by impregnating porous YSZ with salts of Sr, La, and Mn to 40 wt % LSM. The effect of calcination temperature on cathode performance at 973 K was then studied using both symmetric cells and solid oxide fuel cells (SOFCs). Following calcination at 1123 K, the LSM in the composite remained porous. In symmetric-cell tests, LSM(1123)-YSZ electrodes exhibited a low loss, , which was unchanged by polarization; however, in fuel cell tests, the performance was poor at current densities above . Following calcination at 1323 or 1523 K, LSM formed a dense layer coating on the YSZ. In symmetric-cell tests, the composite exhibited an ASR greater than , but this decreased, reversibly, upon cathodic polarization or upon heating in humidified at 973 K. In fuel cell tests, the performance of composites calcined at 1323 K was superior to ones at 1523 K, primarily because the ohmic resistance of the cell was higher after 1523 K, probably due to solid-state reactions with the electrolyte. The optimal conditions for forming impregnated LSM-YSZ cathodes and the reasons for the observed hysteresis in cathode polarization are discussed based on these results.

Influence of cations on active sites of the alkaline earth salts of 12-tungstophosphoric acid: microcalorimetric study

The acidic properties of the alkaline earth salts of 12-tungstophosphoric acid were investigated using ammonia absorption microcalorimetry. The number and the strength of acid sites of these catalysts as well as differential heats of ammonia absorption were determined. As a result of substitution of two protons with one alkaline earth cation, the decrease of both the total number of acid sites and the number of the strongest acid sites characterized by differential heats higher then 150 kJ/mol, compared to the values found in the case of initial 12-tungstophosphoric acid, were noticed. While all protons seem accessible for ammonia in Mg, Ca and Ba salts, in the case of Sr salt less then stoichiometric ammonia sorption was detected which can be explained by steric effect of these divalent cations.

Characterization of Sr-Doped LaCoO3-YSZ Composites Prepared by Impregnation Methods

Porous yttria-stabilized zirconia (YSZ) was impregnated with aqueous solutions of the nitrate salts of Sr, La, and Co to obtain composites of (LSCo) and YSZ. X-ray diffraction showed that the perovskite phase formed after heating to 973 K and conductivities as high as 7 S/cm were achieved at 973 K with only 30 wt % LSCo. Coefficient of thermal expansion (CTE) measurements of the composites with as much as 50 wt % LSCo indicated that the CTEs were much lower than the weighted average of the YSZ and LSCo. Electrochemical measurements using symmetric cells in air indicated that the area-specific resistance (ASR) of the composites could be as low as 0.03 Ω cm2 at 973 K and 0.01 Ω cm2 at 1073 K. These low ASR were verified in a cell with an LSCo-YSZ cathode and a Co-ceria-YSZ anode, which exhibited a total electrode polarization loss of 0.25 Ω cm2 at 973 K and 0.1 Ω cm2 at 1073 K for operation in humidified However, changes in electrochemical performance with time showed that some electrode degradation occurred over a period of 250 h, even at 973 K. © 2004 The Electrochemical Society. All rights reserved.

Lanthanum strontium manganite/yttria-stabilized zirconia nanocomposites derived from a surfactant assisted, co-assembled mesoporous phase.

A one-pot, soft-chemistry, surfactant-assisted co-assembly approach to prepare La(1-x)Sr(x)MnO(3) (LSM)/Y(2)O(3)-stabilized ZrO(2) (YSZ) nanocomposites for use as solid oxide fuel cell (SOFC) cathodes has been investigated. This material with sub-hundred nanometer grain sizes for each phase is the first such nanocomposite where aqueous-based precursors of each component are incorporated in a single synthetic step. This approach utilizes the co-assembly of an anionic yttrium/zirconium acetatoglycolate gel, cetyltrimethylammonium bromide as the cationic surfactant template, and inorganic La, Mn, and Sr salts under alkaline aqueous conditions. The resulting as-synthesized product is an amorphous mesostructured organic/inorganic composite, which is transformed to a mesoporous inorganic oxide with nanocrystalline YSZ walls upon calcination. Calcination to temperatures above 600 degrees C lead to collapse of the mesopores followed by further crystallization of the nanocrystalline YSZ phase and a final crystallization of the LSM perovskite phase above 1000 degrees C. Both the fully crystalline LSM/YSZ and the mesoporous intermediate phase have been investigated for phase homogeneity by TEM energy-dispersive X-ray spectroscopy (EDX) mapping and spot analysis which confirm the dispersion of LSM within a YSZ matrix at the nanometer scale. Impedance spectroscopy analysis of LSM/YSZ nanocomposite electrodes demonstrate a low polarization resistance of around 0.2 omega cm(2) with an activation energy (E(a)) as low as 1.42 eV. Cathodic polarization studies show stable current densities over a 40 h test demonstration.