Al2O3 SiO2 Research Articles

Adjusting photoluminescence of high thermostability Dy3+/Eu3+ co-doped borosilicate glass for white LED device

Due to the adoption of fluorescent powder encapsulated by organic resin, commercial light emitting diodes (LEDs) suffer from low thermal stability and poor light quality under high temperature, and luminescent glass is one of the effective ways to solve this problem. A series of borosilicate (B2O3–SiO2–Al2O3–PbO-Dy2O3–Eu2O3, marked as BSAP: DyEu) was prepared by the gas suspension technique. The basic characterization test indicate that the prepared glass has excellent thermal stability and stable structure. The optical properties of the luminescent glass were investigated in detail. By changing the Eu3+ doping amount, the Dy3+/Eu3+ co-doped glass can realize warm white light emission. The temperature-variable fluorescence spectra of BASP: Dy1.25Eu1.0 were analyzed, and the glass can produce strong warm white light emission in a wide temperature range. At 700 K, the luminous intensity of the glass remains above 38.49 % of the room temperature, and the chroma shift ΔC = 8.57 × 10−3. In addition, the w-LED device based on commercial GaN chip and BSAP: DyEu glass realizes warm white light output with excellent correlated color temperature (3063 K) and high color rendering index (90.3). The analysis shows that Dy3+/Eu3+ co-doped borosilicate glass can be used as a candidate material for w-LED applications.

Ion Exchange Strengthening of Glasses of the ZnO–MgO–Al2O3–SiO2 Glass-Ceramic-Forming System with an Increased Content of Na2O

Ion Exchange Strengthening of Glasses of the ZnO–MgO–Al2O3–SiO2 Glass-Ceramic-Forming System with an Increased Content of Na2O

Printable silicate and RuO2 composite with wide-range linear PTC for high-temperature sensors

3D printing has revolutionised the design and manufacturing of high-temperature thin/thick-film sensors (TFSs). However, existing printable high-temperature materials face cost-performance trade-offs. This study proposes a silicate and RuO2 composite for the 3D printing of TFSs. A silicate compound (SiO2–Al2O3–CaO, SAC) was used as a sintering aid to reduce the sintering temperature of RuO2, forming a silicate glass phase that enhanced film density and substrate adhesion. The SAC also minimised RuO2 particle volatilisation at high temperatures, thus enhancing the stability of the SAC/RuO2 composite. The SAC/RuO2 TFSs demonstrated exceptional performance, with a positive temperature coefficient (502 ppm/°C) from room temperature to 800 °C, high linearity, and stability (resistance drift rate of 0.1 %/h at 800 °C), extending the application temperature of RuO2 by nearly 200 °C from the previous application temperature of 600 °C. Therefore, the SAC/RuO2 composite offers a new low-cost and high-performance solution for using 3D printing technology in harsh environmental sensors such as turbine blades.

Thermodynamic descriptions of the CaO–Al2O3 and CaO–Al2O3–SiO2 systems over the whole composition and temperature ranges

AbstractThe CaO–Al2O3–SiO2 system is a fundamental system in aluminosilicate materials, and its thermodynamic description provides key information for ceramic design, cement production, slag tapping, and geological prediction. However, the existing thermodynamic calculations for the CaO–Al2O3 system show inaccurate heats of formation for the compounds and consequently a decomposition of the CA2 (CaO⋅2Al2O3) phase at a low temperature. Besides, the solid solutions in anorthite and cristobalite have never been considered in the previous thermodynamic assessments for the CaO–Al2O3–SiO2 system. Therefore, thermodynamic reassessments of the CaO–Al2O3 and CaO–Al2O3–SiO2 systems are carried out in the present work using the CALculation of PHAse Diagram method, considering the solid solution in anorthite and cristobalite for the first time. The anorthite and cristobalite phases are modeled based on the individual mechanism of solid solution, with the anorthite described by (Ca+2, Va)1(Al+3, Si+4)2(Si+4)2(O−2)8 and the cristobalite described by (Va, Ca+2)1(Si+4, Al+3)2(O−2)4. The present assessment solves the above issues and provides consistent thermodynamic descriptions for the liquid and solid phases. Based on the established thermodynamic database, a Scheil solidification simulation is carried out for a cement clinker and the variations of mass fractions of the phases as well as the composition of liquid during Scheil cooling are calculated. The present work guides the design of relevant materials and lays an essential foundation for the establishment of the thermodynamic database of multicomponent aluminosilicate materials.

Nanomechanical properties of ceramic materials from the SiO2–Al2O3-(Na2O)–K2O–MgO system with an addition of SrO

The ceramic materials studied in this paper consist of finely dispersed crystalline phases embedded in a glassy matrix, which is similar to glass-ceramic materials, porcelain, and VC products. The strength depends then not only on the properties of the individual crystalline phases but also on their interactions and the matrix. Differences in mechanical properties for materials with similar chemical compositions are most likely related to diverging microstructures. Crystal orientation, grain-size distribution and shape, the ratio of the glass matrix to the crystalline phase, and homogeneity control the flexural strength of glass-ceramic materials. The subject of the study is whiteware ceramic materials from the SiO2–Al2O3–Na2O–K2O–MgO–SrO system, fired similarly to the regime used for VC products. The effect of the type of alkali oxide and the share of SrO were tested. This paper presents the results of hot-stage microscopy, X-ray diffraction (XRD), scanning electron microscopy with a micro-analyzer (SEM-EDS) and biaxial flexural strength measurements. Additionally, nanoindentation technique was used to access local mechanical properties.

Encapsulation of SiC/SiC cladding tubes with excellent mechanical performance and air tightness using a CaO-modified Y2O3–Al2O3–SiO2 glass

Currently, the encapsulation of SiC/SiC has been a key technical challenge limiting further application, and YAS-based glass offered a possible solution. In this paper, different CaO-doped Y2O3–Al2O3–SiO2 (YAS) glass solders were prepared and employed to join SiC/SiC. The joints were all structurally dense with the room temperature shear strengths higher than or equal to ∼51.7 MPa. Notably, joints containing 3.0 wt% CaO exhibited increased shear strength of ∼57.1 MPa, and the shear strength at 1200 °C was about 15.8 MPa in an air environment, meeting the requirements of the LOCA conditions. Optimal performance was achieved by using 3.0 % CaO-doped YAS glass to encapsulate SiC/SiC cladding, yielding a continuous, dense encapsulation region with predominantly small closed pores (≤1.0 mm3). Glass infiltration was found in both the end plug and cladding wall. The joints did not leak after 72h of holding pressure at 15 MPa, indicating their excellent air tightness.

CaO–MgO–Al2O3–SiO2 corrosion resistance of multi-rare-earth-oxide-doped zirconia thermal barrier coating

As a thermal barrier coating (TBC) material, 8 wt% yttria-stabilized zirconia (8YSZ) exhibits poor resistance against calcium–magnesium–aluminosilicate (CMAS) corrosion. This is caused by the penetration of molten CMAS glass and the depletion of Y3+, which limits the lifetime of 8YSZ. In this study, a multi-rare-earth-oxide-doped zirconia (15 wt% (Lu0.2Yb0.2Dy0.2Gd0.2Y0.2)–ZrO2, denoted as 15LYDGY–SZ) ceramic was prepared to examine its interaction with CMAS. The sluggish diffusion effect and the competition between various dopant elements toward reaction with CMAS effectively slow down the atomic diffusion and limit the transformation of tetragonal phase into monoclinic phase in 15LYDGY–SZ ceramic. Compared with the currently used 8YSZ ceramic, the corrosion resistance of 15LYDGY–SZ to CMAS and its retention rate of fracture toughness after CMAS corrosion are improved. The results show that the multi-rare-earth-oxide-doped zirconia ceramic prepared in this study is a promising candidate material for the development of future TBCs.

Correlation of rare earth coordination and spectral properties in Er3+ doped Na2O–Al2O3–SiO2 glasses with different Al2O3 concentrations by molecular dynamics simulations

The molecular structure of Er2O3 doped Na2O–Al2O3–SiO2 glasses with varying Na2O/Al2O3 ratios is explored via molecular dynamics (MD) simulations using the so-called inherent structure sampling method, which allows the calculation of a large number of local structures of low concentration, as needed to determine the surrounding of low concentration dopants. General structural parameters, including radial distribution functions, coordination numbers and interatomic distances of all network forming and network modifying ions are reported. However, in this work, special attention is devoted to the effect of Al2O3 concentration on the local surrounding of the doped Er3+ ions. It is shown that the Er atoms coordinate 5–6 oxygen ions in their first coordination sphere in the investigated glasses. The Er–O coordination number increases monotonically with increasing Al2O3 concentration and decreasing Na2O/Al2O3 ratio. It is found that the Er atoms are preferably connected to non-bridging oxygen atoms (NBO) in all glasses, even in the peraluminous composition. Additionally, the MD simulation results are compared to the glasses spectral properties that were already investigated in detail by Tanabe and Hanada. The increasing Er-NBO coordination number derived by MD simulations could be correlated with the increased peak splitting of the Er3+ absorption peaks reported by Tanabe and Hanada. Furthermore, a correlation between the Judd-Ofelt parameters published by Tanabe and Hanada and the Er3+ coordination in the glass structure is discussed. It is shown that the Er–O coordination increases with increasing Ω2 parameter as the Al2O3 concentration increases in the glass composition. A correlation of the average overall Er–O coordination number with the symmetry of the local Er site is proposed.

Geochemistry and geochronology of the TTG-sanukitoid suite in the Zhulagou area: Constraints on the Neoarchean crustal evolution of the western North China Craton

The Archean basement in the Yinshan Block of the western North China Craton consists of a variety rock of assemblage, including TTG (tonalite-trondhjemite-granodiorite) rocks and some dioritic gneiss (sanukitoid). Understanding the petrogenesis of these rocks is crucial for comprehending the late Neoarchean crustal evolution of the western North China Craton. This study provides a new geochronological, geochemical, and Sr-Nd-Pb-Hf isotopic data for the TTG-sanukitoid suit that was newly identified in the Zhulagou area. The late Neoarchean TTG gneisses were emplaced around 2.54–2.50 Ga, while dioritic gneiss was emplaced between 2.53 and 2.50 Ga. The TTG gneisses exhibit high SiO2 (64.46–72.24 wt%) and Al2O3 (13.37–16.48 wt%) contents, relatively elevated (La/Yb)N and Sr/Y ratios, as well as low Y and Yb contents. They display variable εHf(t) (+0.94 to +3.57) and εNd(t) (−1.02 to +0.82) values, with relatively low Pb isotopic compositions, suggesting that they were derived from the partial melting of a thickened mafic lower crust. On the other hand, dioritic gneiss shows moderate SiO2 (58.05–61.87 wt%) content, high MgO (2.62–4.06 wt%), Al2O3 (14.42–18.44 wt%) and Cr contents, but relatively low (La/Yb)N values, showing geochemical affinity to the Archean sanukitoids. The dioritic gneiss exhibits variable εHf(t) values (−2.29 to +5.56) and εNd(t) (−2.05 to +2.02), with relatively low Pb isotopic compositions. Furthermore, the presence of amphibolite xenoliths, along with the high Mg# contents (36.84–53.49), indicating the addition of mantle-derived components to its source region. Therefore, the formation of the dioritic gneiss is primarily attributed to partial melting of the thickened (mafic) lower crust and the addition of mantle material. By combining previous studies with the new data presented in this study, we propose that a late Neoarchean tectonic regime involving a mantle plume is the most favorable explanation for the two major magmatic events in the Yinshan Block. Firstly, the earlier pulse/stage of mantle plume resulted in the ∼2.7 Ga thickened (mafic) lower crust and a limited amount of TTG rocks. Subsequent pulse/stage of mantle plume triggered partial melting of pre-existing thickened (mafic) lower crust and generated 2.54–2.50 Ga TTG rocks and dioritic gneiss.

Bioinspired directional structures for inhibiting wetting on super-melt-philic surfaces above 1200 °C

Over the past two decades, superhydrophobic surfaces that are easily created have aroused considerable attention for their superior performances in various applications at room temperature. Nowadays, there is a growing demand in special fields for the development of surfaces that can resist wetting by high-temperature molten droplets (>1200 °C) using facile design and fabrication strategies. Herein, bioinspired directional structures (BDSs) were prepared on Y2O3-stabilized ZrO2 (YSZ) surfaces using femtosecond laser ablation. Benefiting from the anisotropic energy barriers, the BDSs featured with no additional modifiers showed a remarkable increase from 9.2° to 60° in the contact angle of CaO–MgO–Al2O3–SiO2 (CMAS) melt and a 70.1% reduction in the spreading area of CMAS at 1250 °C, compared with polished super-CMAS-melt-philic YSZ surfaces. Moreover, the BDSs demonstrated exceptional wetting inhibition even at 1 400 °C, with an increase from 3.3° to 31.3° in contact angle and a 67.9% decrease in spreading area. This work provides valuable insight and a facile preparation strategy for effectively inhibiting the wetting of molten droplets on super-melt-philic surfaces at extremely high temperatures.

Studying the features of complex beryllium-containing silicate phases co-crystallization in zonal samples using the x-ray electron probe microanalysis method

Research subject. Silicate ingots containing four species-forming components Be, Mg, Al, and Si and belonging to the crystallization region of beryllium indialite (with the formula of Mg2BeAl2Si6O18 and a beryl-type structure). Aim. To investigate the fundamental problem of identifying the patterns of matter differentiation and the stable and metastable phase formation in silicate matrices. Methods. The evolution of the phase composition of silicate melts was registered using a temperature gradient method. Results. New data on the features of phase transformations in silicate melts belonging to the region of beryllium indialite were obtained by electron probe microanalysis (EPMA). Co-existing metastable and stable mineral phases were identified, and the similarity of their compositions with different structures was shown. The nature of impurity phases at each stage of crystallization was established. Conclusions. The evolutionary sequence of phase associations ensuring the crystallization of beryllium indialite and metastable phases of a similar composition, the nature of which is determined by the initial ratio of components, was experimentally recorded. The range of possible phase associations that co-crystallize or replace a stable phase with a beryl structure in melts from the region of existence of beryllium indialite in the BeO–MgO–Al2O3–SiO2 system was extended. The selectivity of the coloring element chromium entry into various phases of the studied system is shown depending on the capabilities of their structure. The addition of a chromophore is a reliable criterion for visualizing successive layers, zones, and areas of changing phase associations in the final ingot.

The structure of CaO–MgO–Al2O3–SiO2 melts and glasses doped with FeOX–NiO

AbstractNeutron and x‐ray diffraction measurements have been performed on CaO–MgO–Al2O3–SiO2 (CMAS) glasses doped with NiO–FeXO at room temperature, along with x‐ray measurements on aerodynamically levitated liquids at ≥2000 K. The disordered structures have been modeled using empirical potential structure refinement to investigate the relation between the aluminosilicate network and the modifying cations. The SiO4 and AlO4 tetrahedra are found to have wider Si–O and Al–O bond distance distributions in the glass, and the first Ca–On coordination shell is highly distorted, redistributing different populations of long and short bonds between the liquid and the glass. The addition of Fe and Ni at low aluminosilicate content increases the number of free oxygens not bonded to AlO4 or SiO4. Mg–O and Fe–O are both found to be predominantly fourfold and fivefold in the liquid and glassy states. Despite these low coordination numbers, their bond angle distributions indicate that they are predominantly in nontetrahedral‐type geometries, with ferrous and ferric iron possessing similar coordination environments. The Ca–O and Mg–O average coordination numbers and enthalpies of solution are consistent with their higher reactivity within relatively acidic aluminosilicate melts.

Effects of CaO/SiO2 ratio and CaCl2 content on the densification, microstructure, and properties of sintered CaO–MgO–Al2O3–SiO2–CaCl2 glass-ceramic

The effects of CaO/SiO2 ratio (basicity) and CaCl2 addition amount on the properties of CaO–MgO–Al2O3–SiO2–CaCl2 glass-ceramics (GC) were investigated. When sintered at 825 °C, the increase in basicity from 0.35 to 0.75 reduced the porosity of GCs from 1.1 to 0.8 vol%, but the increase of CaCl2 addition amount from 5 to 10 wt% increased the porosity from 0.8 to 7.0 vol%. The main crystalline phase of GC changed from augite (Ca(Mg0·7Al0.3) (Si1·7Al0.3)O6) to Ca10Al12Cl2Si5O37 by increasing the CaCl2 addition amount to 7.5 wt%. The increase in CaCl2 addition had adverse effects on the bending strength and Vickers hardness, while the rise in basicity deteriorated the bending strength but had little impact on the Vickers hardness. This study may have a guiding significance for preparing slag-based GCs and treating CaCl2-containing wastes.

Characteristics of a CaO–B2O3–SiO2–Al2O3–ZnO-based sandwich substrate and its dielectric properties in the 5G millimeter-wave band

In this study, a 34.5CaO–23B2O3–33.5SiO2–6Al2O3–3ZnO (CBSAZ) glass-ceramic substrate was prepared using a sol–gel method. A porous CaO–B2O3–SiO2–Al2O3–ZnO layer (CBSAZ0.5C) with a porosity of 72.6 % and thickness of 365 μm was inserted between two ∼120 μm thick dense CBSAZ layers to form a tri-layer substrate (CBSAZ/CBSAZ0.5C/CBSAZ). The dielectric constants (εr) and dielectric losses (tanδ) of the dense CBSAZ substrate at 20 and 60 GHz were 6.90 and 0.029, respectively, and 6.96 and 0.017, respectively. These values were almost independent of frequency. In contrast, the εr and tanδ values of the CBSAZ/CBSAZ0.5C/CBSAZ sandwich substrate at 20 and 60 GHz were 3.59 and 0.022, respectively, and 3.11 and 0.020, respectively. Thus, the εr value of the CBSAZ/CBSAZ0.5C/CBSAZ sandwich substrate was significantly lower than that of the CBSAZ substrate, whereas the tanδ and κ values of the CBSAZ/CBSAZ0.5C/CBSAZ and CBSAZ substrates were similar.

A novel Gd2O3–Al2O3–SiO2 glass-ceramics substrate material with comprehensive performance

A novel Gd2O3–Al2O3–SiO2 glass-ceramics (GAS GCS) for substrate application was prepared using the melt-quenching method. The present study pay attention to investigate the crystallization and sintering behaviors, phase compositions, micromorphology, dielectric and mechanical properties of GAS glass-ceramics. An appropriate amount of Gd2O3 diminished the glass viscosity while enhancing structural stability, thereby reducing the activation energy for crystallization and sintering. This contributed to the GAS GCS achieve dense microstructure and high crystallinity. X-ray diffraction (XRD) and Raman spectroscopy analyses confirmed the presence of high-density crystal phases, namely Gd2SiO5 and Gd2Si2O7, which significantly contribute to the enhanced density of the samples. Moreover, a positive correlation was observed between the dielectric constant and crystallinity. Notably, the GAS GCS composition of 41 wt% Gd2O3-21.3 wt% Al2O3-37.7 wt% SiO2 exhibited optimal properties, including a flexural strength of 243.4 MPa, Vickers hardness of 7.77 GPa, elastic modulus of 154.02 GPa, coefficient of thermal expansion of 5.9 × 10−6/°C, dielectric constant of 7.43, and dielectric loss of 4.05 × 10−3. These outstanding characteristics position it as a promising candidate for substrate materials.

Epitaxial growth of gehlenite in CaO–MgO–Al2O3–SiO2 based glass ceramic induced by Nb2O5 addition

In this study, the crystallization behavior of a CaO–MgO–Al2O3–SiO2 based glass ceramics with Nb2O5 addition was investigated by using DSC, XRD and TEM techniques. It was found that three crystalline phases, namely, CaNb2O6, diopside and Gehlenite (Ca2Al2SiO7), were formed from the glass matrix during the crystallization heat treatment. The CaNb2O6 phase was the first to precipitate from the glass matrix at around 850 °C, acting as a nucleating agent that facilitated the formation of Gehlenite (Ca2Al2SiO7) at 900–950 °C. The TEM observation revealed a consistent orientation relationship between the CaNb2O6 and the Gehlenite (Ca2Al2SiO7) phases, indicating that CaNb2O6 could induce the epitaxial growth of Gehlenite (Ca2Al2SiO7). This result provides a new insight into the preparation of Gehlenite epitaxial films and glass ceramics.

Influence of glass-phase structure on the degradation of rare-earth (Y2O3, La2O3)-doped CaO–Al2O3–SiO2–B2O3 glass-ceramics in citric acid solution

Liquid-phase sintering anorthite (LSA) glass-ceramics with degradation in citric-acid solution have been prepared from CaO–Al2O3–SiO2–B2O3 low-melting compositions. By means of the chemical corrosion of the glass phases, LSA glass-ceramics are effectively degraded in the citric acid solution. Then, the influence of B2O3 and rare-earth (RE) on the structures of glass phases, the degradation of LSA glass-ceramics in the citric-acid solutions, and the dielectric properties are investigated systematically. The results suggest that when the B2O3 molar ratio in the composition CaO–Al2O3–SiO2–B2O3 is 0.5, doping LSA glass-ceramics with RE can reduce the quantity of bridging oxygen and [BO4] units in the glass phase, as well as the degree of network connection of [AlO4] units in the glass network. Conversely, when the B2O3 molar ratio is decreased down to 0.3, doping RE into LSA glass-ceramics increases the quantity of bridging oxygen and [BO4] units for glass phase. This improvement in chemical stability effectively impedes the degradation of LSA glass-ceramics in citric-acid solutions. Concurrently, the degradation mechanism of LSA glass-ceramics in citric acid solution is analyzed and explained in terms of classical glass corrosion theory, while the microstructural characteristics of LSA glass-ceramics are utilized to investigate their dielectric properties. It indicates that the dielectric loss and dielectric constant of LSA glass-ceramics are significantly lowered as a result of the existence of the glass phase. Especially when the B2O3 molar ratio in the composition CaO–Al2O3–SiO2–B2O3 is 0.3, and the La2O3 doping percentage into LSA glass-ceramics is 0.5 wt%, the LSA glass-ceramics exhibit the lowest dielectric loss value of 3.13 × 10−3 and εr = 4.17. Developing the LSA glass-ceramic with degradation in organic acids can provide a new idea for the recycling and disposal of e-waste.

Dissolution behavior of Al2O3 inclusions into CaO–MgO–SiO2–Al2O3–TiO2 system ladle slags

Dissolution behavior of Al2O3 inclusions into CaO–MgO–SiO2–Al2O3–TiO2 system ladle slags

Reaction mechanism between carbon and CaO–SiO2–Al2O3–Na2O slag system during continuous casting process

The reaction behavior between the carbon and mold fluxes during the heating process is vital for a successful continuous casting process and the high billet quality. A detailed investigation combined with thermogravimetry-mass spectrometry (TG-MS), differential scanning calorimetry (DSC), X-ray diffraction (XRD), scanning electron microscopy (SEM), Raman spectroscopy, and transmission electron microscopy (TEM) techniques was carried out to systematically investigate the transformation mechanistic of the macro physicochemical properties, melting behavior, viscosity, crystallization, and heat transfer performance caused by the reaction behavior. The results showed that the mold flux underwent carbonate decomposition (973–1223 K), solid reaction (1273–1573 K), and melting process (1473–1673 K) during the continuous casting process. The carbon-bearing mold flux exhibited an endothermic peak at approximately 1673 K, corresponding to a weight loss ratio of approximately 14.5% on the TG curve, confirming that carbon could react with the middle mineral phases Ca2SiO4, Ca2Al2SiO7, and Na6Ca3Si6O18 to form SiC, increasing the breaking temperature by approximately 293 K. SEM and TEM results indicated that the melting behavior was restrained by the carbon itself and the newly formed components. Besides, the addition of carbon increased the degree of polymerization of molten slag, the thickness of slag film and the proportion of small crystals in slag film, further leading to an increase in crystallization and heat transfer performances. The reaction mechanism between carbon and slag and the subsequent effects on melting point, viscosity, crystallization ratio and heat flux density were clearly understood, which is meaningful for the carbon blending process of the mold flux.

Slag Electrical Conductivity and Its Effect on Mass Transport and Interfacial Reaction Kinetics

Pyrometallurgical refining typically involves slag–metal reactions which are commonly controlled by transport of reactants in the slag or metal phase. For the simplicity of analysis, mass transport in slag is generally treated on a phenomenological basis as transport of molecules. Although this approach works well for many of the reaction systems over narrow ranges of conditions, it can fail when extrapolated over a wide range of conditions. In many refining processes, transport of oxygen in slag determines the kinetics of major reactions. Transport of oxygen in slag is strongly influenced by the electrical conductivity of slag. Whilst this has been well understood since the 1950s, there have been relatively few attempts to quantify the effects of slag electrical properties on the refining kinetics. Herein, an overview is presented focusing on the electrical properties of slags and their effects on the transport kinetics in steelmaking reactions. An analysis is conducted based on a modified version of the approach taken by Wagner to describe oxygen transport in solid oxides. Data from the literature including work from the authors’ laboratory is discussed in an evaluation of literature oxygen transport in CaO–SiO2–FetO, CaO–SiO2–Al2O3–FetO, and PbO–Fe2O3 slags.