This paper shows the microstructural differences and phase characterization of pure phases and hydrated products of the cubic and orthorhombic (Na-doped) polymorphs of tricalcium aluminate (C₃A), which are commonly found in traditional Portland cements. Pure, anhydrous samples were characterized using scanning transmission X-ray microscopy (STXM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) and demonstrated differences in the chemical and mineralogical composition as well as the morphology on a micro/nano-scale. C₃A/gypsum blends with mass ratios of 0.2 and 1.9 were hydrated using a water/C₃A ratio of 1.2, and the products obtained after three days were assessed using STXM. The hydration process and subsequent formation of calcium sulfate in the C₃A/gypsum systems were identified through the changes in the L edge fine structure for Calcium. The results also show greater Ca L binding energies between hydrated samples with different gypsum contents. Conversely, the hydrated samples from the cubic and orthorhombic C₃A at the same amount of gypsum exhibited strong morphological differences but similar chemical environments.
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http://dx.doi.org/10.3390/ma9090745 | DOI Listing |
Acta Crystallogr B Struct Sci Cryst Eng Mater
February 2025
CSIRO Division of Mineral Products, Port Melbourne, Victoria, Australia.
The crystallographic phase change from tetragonal litharge (α-PbO; P4/nmm) to orthorhombic massicot (β-PbO; Pbcm) has been studied by full-matrix Rietveld analysis of high-temperature neutron powder diffraction data collected in equal steps from ambient temperature up to 925 K and back down to 350 K. The phase transformation takes place between 850 and 925 K, with the coexisting phases having equal abundance by weight at 885 K. The product massicot remains metastable on cooling to near ambient temperature.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Department of Materials Science and Engineering, Feng Chia University, Taichung City, 40724, Taiwan.
The unique optical properties of perovskite quantum dots (PQDs), particularly the tunable photoluminescence (PL) across the visible spectrum, make them a promising tool for chlorinated detection. However, the correlation between the fluorescence emission shift behavior and the interface of phase transformation in PQDs has not been thoroughly explored. In this study, we synthesized CsPbBr PQDs via the hot-injection method and demonstrated their ability to detect chlorinated volatile compounds such as HCl and NaOCl through a halide exchange process between the PQDs' solid thin film and the chlorinated vapor phase.
View Article and Find Full Text PDFDalton Trans
January 2025
Graduate School of Engineering and Science, Shibaura Institute of Technology, 307 Fukasaku, Minuma, Saitama, 337-8570, Japan.
We successfully synthesized perovskite-type RbTaO at 1173 K under 4 GPa. RbTaO crystalized as a cubic system (3̄ space group (SG), = 4.04108(3) Å) at 300 K in contrast to the orthorhombic perovskite-type RbNbO prepared under the same conditions.
View Article and Find Full Text PDFDiscov Nano
January 2025
Instituto de Ciencia de Materiales de Madrid, CSIC, Cantoblanco, 28049, Madrid, Spain.
Chemically tuned organic-inorganic hybrid halide perovskites based on bromide and chloride anions CH(NH)Pb(BrCl) (CH(NH): formamidinium ion, FA) have been crystallized and investigated by neutron powder diffraction (NPD), single crystal X-ray diffraction (SCXRD), scanning electron microscopy (SEM) and UV-vis spectroscopy. FAPbBr and FAPbCl experience successive phase transitions upon cooling, lowering the symmetry from cubic to orthorhombic phases; however, these transitions are not observed for the mixed halide phases, probably due to compositional disorder. The band-gap engineering brought about by the chemical doping of FAPb (BrCl) perovskites (x = 0.
View Article and Find Full Text PDFSci Rep
December 2024
Department of Chemistry, Faculty of Science, Umm Al-Qura University, Makkah, 21955, Saudi Arabia.
Malachite green is a hazardous chemical that poses serious threats to aquatic ecosystems due to its toxicity and persistence in the environment. Additionally, it is harmful to human health, recognized as a carcinogenic and mutagenic agent that can cause long-term adverse effects. Hence, in this study, malachite green dye was efficiently removed from aqueous media using CoO/MgO/MgBO novel nanocomposites, known as CBM600 and CBM800.
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