High-Temperature Creep Behavior of Mixed Conducting La0.5Sr0.5Fe1−xCoxO3-δ (0.5≤x≤1) Materials

Steady-state compressive creep rate of La_0.5Sr_0.5Fe_0.5Co_0.5O_3−δ (LSFC) and La_0.5Sr_0.5CoO_3−δ (LSC) is reported in the temperature region 900°–1050°C and stress range 5–28 MPa. The stress exponents for the two materials were 1.71±0.18 and 1.24±0.15, respectively. The activation energy for creep was considerably higher for LSC (619±56 kJ/mol) than for LSFC (392±28 kJ/mol). The grain size exponent for LSC was 1.28±0.14. Considerably higher creep rates were observed for both materials in N₂ compared with air. Relaxation by creep of chemical-induced stresses in oxygen-permeable membranes is addressed, especially at low partial pressure of oxygen.     

Sintering behaviour of La1−xSrxFeO3−δ mixed conductors

The sintering properties of La_1−xSr_xFeO_3−δ (x = 0.1, 0.25) mixed conductors have been investigated with particular emphasis on the effect of secondary phases due to cation non-stoichiometry (±5 mol% La excess and deficiency). Secondary phases, located at grain boundaries in cation non-stoichiometric materials, increased the sintering temperature compared to single-phase materials. Extensive swelling in final stage of sintering was observed in all materials, which resulted in micro-porous materials. The swelling was most pronounced in the phase pure and two-phase materials due to La-deficiency, while refractory secondary phases in La-excess materials inhibited both sintering, grain growth and swelling. In La-deficient materials, formation of molten secondary phases resulted in rapid swelling due to viscous flow. The present findings demonstrated the importance of controlling sintering temperature and time, as well as careful control of the cation stoichiometry of La_1−xSr_xFeO_3−δ in order to achieve fully dense and homogenous La_1−xSr_xFeO_3−δ ceramics.     

Participation of Danish and immigrant cleaners in a 1-year worksite intervention preventing physical deterioration

Worksite health promotion is seldom offered to workers who are low-educated and multi-ethnic, possibly due to an assumption that they are more reluctant to participate. Furthermore, little has been done to promote health at female-dominated workplaces. The main aim of this study was to investigate differences in participation among immigrant and Danish cleaners throughout a 1-year randomised controlled study tailored to cleaners and carried out in predominantly female workplaces. No significant differences in ethnicity were found in consent and participation throughout the 1-year intervention. Dropout was equally distributed among Danish and immigrant cleaners. This study indicates that a worksite health promotion intervention among a female-dominated, high-risk occupation such as cleaning can be equally appealing for Danes and immigrants. PRACTITIONER SUMMARY: This study provides insight about participation of Danish and immigrant cleaners in a worksite health promotion intervention in a predominantly female occupation. For attaining high participation and low dropout in future worksite health promotion interventions among cleaners, the intervention ought to not only target the ethnic background of the workers, but also to be specifically tailored to the job group.     

Effect of CO2 Exposure on the Chemical Stability and Mechanical Properties of BaZrO3‐Ceramics

The reactivity of BaZrO₃ with CO₂ has been addressed as one of the major challenges with BaZrO₃‐based electrolytes in protonic ceramic fuel cells. Here, we present a study of the effect of CO₂ exposure on BaZrO₃‐materials at elevated temperatures. Dense BaZr_1?xY_xO_3?x/2 (x = 0, 0.05, 0.1, 0.2) and BaCe_0.2Zr_0.7Y_0.1O_2.95 ceramics were prepared by sintering of powder prepared by spray pyrolysis. The Vickers indentation method was used to determine the hardness and estimate the fracture toughness of pristine materials as well as the corresponding materials exposed to CO₂. Formation of BaCO₃ on the surface of exposed ceramics was confirmed by X‐ray diffraction and electron microcopy. The reaction resulted in formation of Ba‐deficient perovskite at the exposed surface. The reaction with CO₂ was most pronounced at 650°C compared to the other temperatures applied in the study. The reactivity was also shown to depend on the Y‐content and the grain size and was most pronounced for BaZr_0.9Y_0.1O_2.95. The reaction with CO₂ was observed to have a profound effect on the fracture toughness of the ceramics, demonstrating a depression of the mechanical stability of the materials. The results are discussed with respect to the chemical and mechanical stability of BaZrO₃ materials, with particular emphasis on the composition and grain size.     

Reactions between Strontium-Substituted Lanthanum Manganite and Yttria-Stabilized Zirconia: II, Diffusion Couples

Formation of secondary phases and diffusion of cations in diffusion couples of yttria-stabilized zirconia and lanthanum manganite substituted with 0 to 60 mol% strontium have been studied by scanning electron microscopy and energy dispersive X-ray spectroscopy. Only the primary phases were observed after 120 h at 1200°C, while formation of secondary phases was identified already after 1 h heat treatment at 1350°C. The phase composition of the reaction layer altered from La₂Zr₂O₇ to SrZrO₃ at increasing Sr content in La _x Sr_{1- x} MnO₃. The thickness of the reaction layer was increasing with heat treatment time. In diffusion couples of La_0.4Sr_0.6MnO₃ formation of manganese oxide was observed in the perovskite layer after 1 h heat treatment at 1350°C, while isolated grains of SrZrO₃ relatively deep inside the zirconia were observed after longer heat treatment time. Diffusion of Mn into zirconia was observed preferenced along grain boundaries in the early stage of the interface reaction.     

Kinetic Energy Approach to Dissolving Axisymmetric Multiphase Plumes

A phenomenological kinetic energy theory of buoyant axisymmetric multiphase plumes is constructed, with particular attention to the modeling of the dispersed phase. The dissolution is treated by means of the Ranz-Marshall equation involving a mass-transfer coefficient dependent on the plume properties. The model is compared with various experiments, yielding satisfactory agreement. A central ingredient in the model is the turbulent correlation parameter I, playing a role analogous to the conventional entrainment coefficient α. We use experimental data to suggest a relationship between I, the initial gas flux at the source, and the depth of the gas release.     

Template-assisted synthesis of PbTiO3 nanotubes

Nanotubes of ferroelectric lead titanate (PbTiO₃) have been made by a template-assisted method. An equimolar Pb–Ti sol was dropped onto porous alumina membranes and penetrated into the channels of the template. Single-phase PbTiO₃ perovskite nanotubes were obtained by annealing at 700 °C for 6 h. The nanotubes had diameters of 200–400 nm with a wall thickness of approximately 20 nm. Excess PbO or annealing in a Pb-containing atmosphere was not necessary in order to achieve single-phase PbTiO₃ nanotubes. The influence of the heating procedure and the sol concentration is discussed.     

Decomposition and Crystallization of a Sol–Gel-Derived PbTiO3 Precursor

A lead titanate (PbTiO₃) precursor, prepared by the Pechini method, has been heat treated to study the transformation from amorphous to crystalline PbTiO₃. Nucleation of PbTiO₃ in the temperature interval 400°–475°C occurred before completion of the thermal decomposition of the polymeric precursor, resulting in nanocrystalline PbTiO₃ with an unexpectedly high tetragonality ( c/a ratio). Annealing and crystallite growth at 600°C resulted in an increasing c/a ratio with annealing time in line with the expected finite size effect of PbTiO₃. The unusually high c/a ratios observed in PbTiO₃ nucleated at 400°–475°C are discussed in relation to partial reduction and point defects in PbTiO₃.     

Surface Diffusion of Oxygen Transport Membrane Materials Studied by Grain‐Boundary Grooving

Mass transport mechanism responsible for grain‐boundary grooving during thermal annealing of polished ceramics of Ba_0.5Sr_0.5Co_0.8Fe_0.2O_3‐δ (BSCF) and La₂NiO_4+δ (LN) was revealed by atomic force microscopy. Surface diffusion mechanism was confirmed for both materials by the evolution of the grain‐boundary width (w) with annealing time (t), and the surface diffusion coefficient was determined from the slope of w versus t^1/4 following the theory by Mullins. An Arrhenius temperature dependence of the surface diffusion was observed, and the activation energy was determined to be 220 ± 30 and 450 ± 30 kJ/mol, respectively, for BSCF and LN. The surface diffusion data are discussed with respect to similar data for other oxide materials and cation and oxygen anion diffusion in BSCF and LN. Finally, the dihedral angle for both LN and BSCF was determined, and these are typical in the range reported for other oxide materials.