Precipitation selectivity of perovskite phase from Ti-bearing blast furnace slag under dynamic oxidation conditions

The effects of dynamic oxidations on the crystal morphology and the precipitation behavior of the perovskite phase from Ti-bearing blast furnace slag were investigated. Air was blown into the molten slag as an oxygen source through a lance during the dynamic oxidation process. It was found that the dispersed Ti components were selectively taken into the perovskite phase (CaTiO₃), and the perovskite phase could be selectively precipitated and grown. Oxidation of molten slag produced a large amount of heat, which not only increased the temperature of the slag, but also promoted the precipitation and growth of the perovskite phase. It was confirmed by isothermal experiments and non-isothermal pilot experiments that the precipitation of the perovskite (CaTiO₃) in molten slag is obviously affected by operation factors such as oxidizing time, and slag temperature. The perovskite phase precipitation kinetics and mechanisms from molten slag during the dynamic oxidation processes were also investigated.     

Viscosity and glass transition temperature of hydrous float glass

Viscosity of water-bearing float glass (0.03-4.87 wt% H₂O) was measured in the temperature range of 573-1523 K and pressure range of 50-500 MPa using a parallel plate viscometer in the high viscosity range and the falling sphere method in the low viscosity range. Melt viscosity depends strongly on temperature and water content, but pressure up to 500 MPa has only minor influence. Consistent with previous studies on aluminosilicate compositions we found that the effect of dissolved water is most pronounced at low water content, but it is still noticeable at high water content. A new model for the calculation of the viscosities as a function of temperature and water content is proposed which describes the experimental data with a standard deviation of 0.22 log units. The depression of the glass transition temperature T_g by dissolved water agrees reasonably well with the prediction by the model of Deubener [J. Deubener, R. Müller, H. Behrens, G. Heide, J. Non-Cryst. Solids 330 (2003) 268]. Using water speciation measured by near-infrared spectroscopy we infer that although the effect of OH groups in reducing T_g is larger than that of H₂O molecules, the difference in the contribution of both species is smaller than predicted by Deubener et al. (2003). Compared to alkalis and alkaline earth elements the effect of protons on glass fragility is small, mainly because of the relatively low concentration of OH groups (max. 1.5 wt% water dissolved as OH) in the glasses.     

Glass viscosity as a function of temperature and composition: A model based on Adam-Gibbs equation

This paper shows that a generalized Adam-Gibbs relationship reasonably approximates the real behavior of glasses with four temperature-independent parameters of which two are linear functions of the composition vector. The equation is subjected to two constraints, one requiring that the viscosity-temperature relationship approaches the Arrhenius function at high temperatures with a composition-independent pre-exponential factor and the other that the viscosity value is independent of composition at the glass-transition temperature. Several sets of constant coefficients were obtained by fitting the generalized Adam-Gibbs equation to data of two glass families: float glass and Hanford waste glass. Other equations (the Vogel-Fulcher-Tammann equation, original and modified, the Avramov equation, and the Douglass-Doremus equation) were fitted to a float-glass data series and compared with the Adam-Gibbs equation, showing that Adam-Gibbs glass appears an excellent approximation of real glasses even as compared with other candidate constitutive relations.     

Effect of P2O5 on the early stage crystallization of K-fluorrichterite glass-ceramics

The addition of 2 mol% P₂O₅ to stoichiometric K-fluorrichterite (KNaCaMg₅Si₈O₂₂F₂, KFR) has been reported to enhance the mechanical properties and improve the in vitro biocompatibility of this glass-ceramic by promoting the formation of enstatite and fluorapatite (FA). Here, the effect of further increasing the P₂O₅ concentration on phase evolution of KFR has been investigated. XRD data showed that mica crystallized in samples with 4 and 5 mol% P₂O₅ (GP4 and GP5, respectively) at 650 °C, but no diopside was detected at higher temperatures, in contrast with the general phase evolution in KFR based glass-ceramics. More importantly, however, the addition of ?4 mol% P₂O₅ induced phase separation of the glass into a silica glass matrix and phosphate rich droplets prior to crystallization. EDS traces taken from samples heat-treated at 600 °C, revealed that the silica glass matrix was deficient in Mg and unlikely to be the host for crystallization of mica. Conversely, the P₂O₅ rich regions contained excess Mg and were considered to be the host for the formation of mica and FA.     

Effect of BaO content on the sintering and physical properties of BaO-B2O3-SiO2 glasses

A BaO-B₂O₃-SiO₂ glass system was chosen as a candidate composition for the application to Pb-free low temperature sinterable glass. The effect of BaO content on the crystallization, sintering behavior, and properties of the glasses was examined. Both the glass transition temperature and crystallization temperature decreased as the BaO content increased. Crystallization easily occurred during sintering with a BaO content of more than 50 mol%, which effectively inhibited the over-firing phenomenon. The dielectric characteristics and thermal expansion coefficient of the glasses were examined and the results were explained on the basis of the crystallization and densification of the specimens.     

Theory of fluidity of liquids, glass transition, and melting

This is a presentation of a rigorous theory of fluidity of liquids, glass transition and melting of solids in the frame of an asymmetric double well potential model. Potential wells are doubled time to time by the local density fluctuations caused by the thermal longitudinal waves. The average frequency of doubling of potential wells is equal to the frequency of the most energetic waves which obey a law similar to Wein’s displacement law in black body radiation. Based on the equilibrium thermodynamic theory of fluctuations and the displacement law, a law of linear pre-diffusion mean-square displacement of particles in a solid is derived: the mean-square displacement of molecules within their potential wells increases linearly with temperature. It is shown that when this is broken-down (where the mean-square displacement at a certain temperature rapidly changes its slope as a function of temperature) glass devitrifies and crystal melts, and all possible solid-liquid transitions of a substance occur at the same critical mean-square displacement: any solid (not only crystals) transforms into liquid when the mean-square displacement, as a fraction of the average intermolecular distance, acquires a certain universal critical value - the same for different substances. It is proved that molecules in a liquid perform specific Brownian motion. The average jump distance is a function of temperature and it is much smaller than the nearest intermolecular distances. At a certain temperature, shown to be the Kauzmann temperature, the average jump distance of Brownian motion becomes equal to zero: the super-cooled liquid undergoes glass transition. The transition was proven to be a phase transition of the fourth order: the free energy of the system and its first, second and third derivatives are all continuous functions, but its fourth derivative with respect to temperature is discontinuous. Molecular mobility, diffusion and viscosity are obtained as functions of temperature.     

Improvement of the Tm:H4 level lifetime in silica optical fibers by lowering the local phonon energy

The role of some glass network modifiers on the quantum efficiency of the near-infrared fluorescence from the ³H₄ level of Tm³⁺ ion in silica-based doped fibers is studied. Modifications of the core composition affect the spectroscopic properties of Tm³⁺ ion. Adding 17.4 mol% of AlO_3/2 to the core glass caused an increase of the ³H₄ level lifetime up to 50 μs, 3.6 times higher than in pure silica glass. The quantum efficiency was increased from 2% to approximately 8%. On the opposite, 8 mol% of PO_5/2 in the core glass made the lifetime decrease down to 9 μs. These changes of Tm³⁺ optical properties are assigned to the change of the local phonon energy to which they are submitted by modifiers located in the vicinity of the doping sites. Some qualitative predictions of the maximum achievable quantum efficiency are possible using a simple microscopic model to calculate the non-radiative de-excitation rates.     

Fabrication and properties of novel low-melting glasses in the ternary system ZnO-Sb2O3-P2O5

Glasses in the ternary system ZnO-Sb₂O₃-P₂O₅ were investigated as potential alternatives to lead based glasses for low temperature applications. The glass-forming region of ZnO-Sb₂O₃-P₂O₅ system has been determined. Structure and properties of the glasses with the composition (60 − x)ZnO-xSb₂O₃-40P₂O₅ were characterized by infrared spectra (IR), differential thermal analysis (DTA) and X-ray diffraction (XRD). The results of IR indicated the role of Sb³⁺ as participant in glass network structure, which was supported by the monotonic and remarkable increase of density (ρ) and molar volume (V_M) with increasing Sb₂O₃ content. Glass transition temperature (T_g) and thermal stability decreased, and coefficient of thermal expansion (α) increased with the substitution of Sb₂O₃ for ZnO in the range of 0-50 mol%. XRD pattern of the heat treated glass containing 30 mol% Sb₂O₃ indicated that the structure of antimony-phosphate becomes dominant. The improved water durability of these glasses is consistent with the replacement of easily hydrated phosphate chains by corrosion resistant P-O-Sb bonds. The glasses containing ?30 mol% Sb₂O₃ possess lower T_g (<400 °C) and better water durability, which could be alternatives to lead based glasses for practical applications with further composition improvement.     

Effect of rogue particles on the sub-surface damage of fused silica during grinding/polishing

The distribution and characteristics of surface cracks (i.e., sub-surface damage or scratching) on fused silica formed during grinding/polishing resulting from the addition of rogue particles in the base slurry has been investigated. Fused silica samples (10 cm diameter × 1 cm thick) were: (1) ground by loose abrasive grinding (alumina particles 9-30 μm) on a glass lap with the addition of larger alumina particles at various concentrations with mean sizes ranging from 15 to 30 μm, or (2) polished (using 0.5 μm cerium oxide slurry) on various laps (polyurethane pads or pitch) with the addition of larger rogue particles (diamond (4-45 μm), pitch, dust, or dried Ceria slurry agglomerates) at various concentrations. For the resulting ground samples, the crack distributions of the as-prepared surfaces were determined using a polished taper technique. The crack depth was observed to: (1) increase at small concentrations (>10⁻⁴ fraction) of rogue particles; and (2) increase with rogue particle concentration to crack depths consistent with that observed when grinding with particles the size of the rogue particles alone. For the polished samples, which were subsequently etched in HF:NH₄F to expose the surface damage, the resulting scratch properties (type, number density, width, and length) were characterized. The number density of scratches increased exponentially with the size of the rogue diamond at a fixed rogue diamond concentration suggesting that larger particles are more likely to lead to scratching. The length of the scratch was found to increase with rogue particle size, increase with lap viscosity, and decrease with applied load. At high diamond concentrations, the type of scratch transitioned from brittle to ductile and the length of the scratches dramatically increased and extended to the edge of the optic. The observed trends can be explained semi-quantitatively in terms of the time needed for a rogue particle to penetrate into a viscoelastic lap. The results of this study provide useful insights and ‘rules-of-thumb’ relating scratch characteristics observed on surfaces during optical glass fabrication to the characteristics of the rogue particles causing them and their possible source.     

Effects of dimethyldiethoxysilane addition on the sol-gel process of tetraethylorthosilicate

The effects of dimethyldiethoxysilane (DDS) addition on the sol-gel process of tetraethylorthosilicate (TEOS) were investigated by varying the addition-time of DDS to acid-catalyzed TEOS solutions in different water contents. At a low water content, the solution is transparent until gelation takes place, while at a high water content, phase separation occurs and leads to hydrophobic particles which, according to scanning electron microscopy-energy dispersive X-ray analysis (SEM-EDX) and thermogravimetric (TG) analysis, show different morphology and thermal behavior. The reaction between TEOS and DDS in different water contents and the structure of final polymers are discussed.     

Influence of the melting conditions of heavy metal oxide glasses containing bismuth oxide on their optical absorption

Glasses of the systems Bi₂O₃-SiO₂, Bi₂O₃-PbO-Ga₂O₃, Bi₂O₃-PbO-Ga₂O₃-GeO₂ and Bi₂O₃-GeO₂-Li₂O have been prepared and the interaction of their melts with crucibles of different materials has been analytically determined. Silica and porcelain crucibles were very strongly corroded and the glass composition was noticeably altered. Instead platinum crucibles are not affected if the Bi₂O₃ content is not too high. The color of the glasses changes in all cases from pale yellow to deep brown when the melting temperature reaches approximately 1000 °C. The higher the temperature and the Bi₂O₃ content the darker the brown color, independently of the nature of the employed crucible. The addition of oxidizing ions (Sb⁵⁺, As⁵⁺ or Ce⁴⁺) to the glass batch prevents darkening. Nanoparticles of elementary bismuth Bi⁰ are observed by transmission electron microscopy in the glasses melted above 1000 °C. The partial thermoreduction of the Bi₂O₃ during the heating of the glass melt is proposed as the mechanism responsible for the observed darkening.     

The effect of HF/NH4F etching on the morphology of surface fractures on fused silica

The effects of HF/NH₄F, wet chemical etching on the morphology of individual surface fractures (indentations, scratches) and of an ensemble of surface fractures (ground surfaces) on fused silica glass has been characterized. For the individual surface fractures, a series of static or dynamic (sliding) Vickers and Brinnell indenters were used to create radial, lateral, Hertzian cone and trailing indentation fractures on a set of polished fused silica substrates which were subsequently etched. After short etch times, the visibility of both surface and subsurface cracks is significantly enhanced when observed by optical microscopy. This is attributed to the increased width of the cracks following etching, allowing for greater optical scatter at the fracture interface. The removal of material during etching was found to be isotropic except in areas where the etchant has difficulty penetrating or in areas that exhibit significant plastic deformation/densification. Isolated fractures continue to etch, but will never be completely removed since the bottom and top of the crack both etch at the same rate. The etching behavior of ensembles of closely spaced cracks, such as those produced during grinding, has also been characterized. This was done using a second set of fused silica samples that were ground using either fixed or loose abrasives. The resulting samples were etched and both the etch rate and the morphology of the surfaces were monitored as a function of time. Etching results in the formation of a series of open cracks or cusps, each corresponding to the individual fractures originally on the surface of the substrate. During extended etching, the individual cusps coalesce with one another, providing a means of reducing the depth of subsurface damage and the peak-to-valley roughness. In addition, the material removal rate of the ground surfaces was found to scale with the surface area of the cracks as a function of etch time. The initial removal rate for the ground surface was typically 3.5× the bulk etch rate. The evolving morphology of ground surfaces during etching was simulated using an isotropic finite difference model. This model illustrates the importance that the initial distributions of fracture sizes and spatial locations have on the evolution of roughness and the rate at which material is removed during the etching process. The etching of ground surfaces can be used during optical fabrication to convert subsurface damage into surface roughness thereby reducing the time required to produce polished surfaces that are free of subsurface damage.     

Effects of morphologies on the field emission characteristics of GaN nanorods grown on Si (0 0 1) by MBE

GaN nanorods were grown on Si (0 0 1) substrates with a native oxide layer by molecular beam epitaxy. The changes in the morphologies and their effects on the field emission characteristics of GaN nanorods were investigated by varying growth conditions, namely, growth time of low-temperature GaN buffer layer, growth time of GaN nanorods, Ga flux during growth of GaN nanorods, and growth temperature of GaN nanorods. GaN nanorods with a low aspect ratio measured by diode configuration showed better field emission characteristics than those with a high aspect ratio, which may be due to the effects of screening and the surface depletion layer. In addition, the distance between the GaN nanorods and the anode played an important role in the field emission characteristics such as turn-on field, field enhancement factor, and field distribution on the emitter surface.     

Study on the device characteristics of FePc and FePcCl organic thin film Schottky diodes: Influence of oxygen and post deposition annealing

Device characteristics of Al/FePc/Au and Al/FePcCl/Au are performed and found to show rectification properties. The basic diode parameters of the device are determined. The electrical conductivity has been measured both after exposure to oxygen for 20 days and after annealing at temperature up to 473 K. Current density-voltage characteristics under forward bias are found to be due to ohmic conduction at lower voltage regions. At higher voltage regions there is space charge limited conductivity (SCLC) controlled by a discrete trapping level above the valance edge. The electrical parameters of oxygen doped and annealed samples in the ohmic and SCLC region are determined. The reverse bias curves are interpreted in terms of a transition from electrode-limited Schottky emission to the bulk-limited the Poole-Frenkel effect. The Schottky barrier parameters of oxygen doped and annealed structures of FePc and FePcCl are determined from the C²-V characteristics.     

Effect of the annealing process on the microstructure of La2Zr2O7 thin layers epitaxially grown on LaAlO3 by metalorganic decomposition

La₂Zr₂O₇ (LZO) films have been grown by metalorganic decomposition (MOD) to be used as buffer layers for coated conductors. A characteristic feature of LZO thin films deposited by MOD is the formation of nanovoids in an almost single crystal structure of LZO pyrochlore phase. Annealing parameters (heating ramp, temperature, pressure, etc.) were varied to establish their influence on the microstructure of the LZO layers. X-ray diffraction (XRD) and transmission electron microscopy (TEM) were used for sample characterization. The epitaxial pyrochlore phase was obtained for annealing temperatures higher than 850 °C whatever the other annealing conditions. However, the film microstructure, in particular, nanovoids shape and size, is strongly dependent on heating ramp and pressure during annealing. When using low heating ramp, percolation of voids creates diffusion channels for oxygen which are detrimental for the substrate protection during coated conductor fabrication. From this point of view high heating rates are more adapted to the growth of LZO layers.