ABSTRACT
In general, phosphate cements have a very rapid setting reaction at room temperature. The same holds for copper slag-based phosphate cements. This means that using them as a binder, for instance as mortar, is always possible on a small scale, but very difficult on a large scale. In this paper, the heat treatment of the copper slag was shown to be an effective way to increase the setting time and keep the mix workable for an adequate period. The main objective of this research was to examine the changes in the phase composition of quenched copper slag after exposure to 500 °C and to evaluate the impact of these changes on the reactivity of the material in an acidic environment, as well as on the mechanical properties, microstructure, and structure of the produced phosphate cement materials. Various experimental methods were utilized to characterize the raw materials and the obtained phosphate cementitious materials, including isothermal microcalorimetry (TAM Air), thermogravimetric analysis (TGA), infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), as well as the determination of the chemical composition using X-ray fluorescence (XRF) and the particle size distribution. Furthermore, compressive strength tests were conducted to gauge the mechanical resistance of the materials. The main findings of this work revealed that subjecting the copper slag to a thermal treatment of 500 °C induced a partial transformation in its structure. The high temperature caused the oxidation of some of the divalent iron oxide in the slag, leading to the formation of hematite. This treatment increased the setting time and reduced the reactivity of the copper slag with phosphoric acid, ultimately enabling the production of a dense phosphate-based cementitious material with outstanding mechanical properties. The compressive strength of the newly developed cement was recorded to be greater than 78.9 MPa after 7 days, and this strength continued to increase, reaching 82.5 MPa after 28 days.
ABSTRACT
In this study, undoped and (Erbium, Ytterbium) co-doped ZnO nanopowders were prepared using the sol-gel method and the supercritical drying of ethyl alcohol. Doping ZnO nanopowders were elaborated with 5 mol% of Er (5 Er: ZnO), 5 mol% of Er and 5 mol% of Yb (5 Er, 5 Yb: ZnO), and 5 mol% of Er and 10 mol% of Yb (5 Er, 10 Yb: ZnO) concentrations. The effects of the Yb concentration on the structural, morphological, photoluminescent, and electrical properties of the ZnO nanopowders were investigated. The main findings of this work were the crystallinization of all of the nanopowders in a hexagonal Wurtzite structure with a spheroidal morphology and a size of 60 nm. Hence, the doping concentration would affect the crystallinity and the morphology of the ZnO nanopowder. The UC (Up-Conversion) emissions were investigated under a 980 nm excitation. It was observed that (Er, Yb: ZnO) exhibited green, ranging between 525 nm and 550 nm and red up-converted emissions of 655 nm, due to the efficient energy transfer process between Er3+ and Yb3+. The absolute quantum yield percentage (QY %) of the doped nanopowders was measured as a function of power density at each up-converted emission. This would prove that (5 Er, 5 Yb: ZnO) had the highest QY percentage value of 6.31 ± 0.2% at a power density of 15.7 W/cm2. Additionally, it had the highest excited state lifetime for green and red emissions. Moreover, the Hall effect measures showed that the resistivity decreased while the electron mobility increased after doping, suggesting that most of rare earth ions were located in the interstitial positions. The carrier concentration increased after doping until (5 Er, 5 Yb: ZnO), suggesting that the Zn2+ ions substituted the RE3+ ions. Then, the carrier concentration decreased, suggesting that doping with higher concentrations would cause grain boundary defects. These findings would suggest that (5 Er, 5 Yb: ZnO) would have the best electrical properties and the lowest band gap energy (3.24 eV). Therefore, the presented preparation of the (Er, Yb: ZnO) nanopowders elaborated, using the sol-gel process would be a potential interesting material for UC applications.
