The present study investigates thermally induced crystallization and phase evolution of amorphous calcium phosphate (ACP) partially substituted with Fe3+ ions (M/P = 1.5 : 1). It was demonstrated that the...

In this study, a highly crystalline bismuth ferrite (BFO) powder was synthesized using a novel, very simple, and cost-effective synthetic approach. It was demonstrated that the optimal annealing temperature for the preparation of highly-pure BFO is 650 °C. At lower or higher temperatures, the formation of neighboring crystal phases was observed. The thermal behavior of BFO precursor gel was investigated by thermogravimetric and differential scanning calorimetry (TG-DSC) measurements. X-ray diffraction (XRD) analysis and Mössbauer spectroscopy were employed for the investigation of structural properties. Scanning electron microscopy (SEM) was used to evaluate morphological features of the synthesized materials. The obtained powders were also characterized by magnetization measurements, which showed antiferromagnetic behavior of BFO powders.

In the present work, three different Mn2+-doped calcium pyrophosphate (CPP, Ca2P2O7) polymorphs were synthesized by wet co-precipitation method followed by annealing at different temperatures. The crystal structure and purity were studied by powder X-ray diffraction (XRD), Fourier-transform infrared (FTIR), solid-state nuclear magnetic resonance (SS-NMR), and electron paramagnetic resonance (EPR) spectroscopies. Scanning electron microscopy (SEM) was used to investigate the morphological features of the synthesized products. Optical properties were investigated using photoluminescence measurements. Excitation spectra, emission spectra, and photoluminescence decay curves of the samples were studied. All Mn-doped polymorphs exhibited a broadband emission ranging from approximately 500 to 730 nm. The emission maximum was host-dependent and centered at around 580, 570, and 595 nm for γ-, β-, and α-CPP, respectively.

The present study investigates the influence of annealing conditions on phase transformations in calcium phosphates. Synthetic brushite (CaHPO4∙2H2O) with Ca/P ratio 1:1 was taken as a starting material and annealed...

In the present work, beta-calcium pyrophosphate (β-Ca2P2O7) was investigated as a potential adsorbent for the removal of heavy metal ions from water. Single-phase β-Ca2P2O7 powders were synthesized by a simple, scalable and cost-effective wet precipitation method followed by annealing at 800 °C, which was employed for the conversion of as-precipitated brushite (CaHPO4∙2H2O) to β-Ca2P2O7. Physicochemical properties of the sorbent were characterized by means of X-ray diffraction (XRD) analysis, Fourier transform infrared spectroscopy (FTIR), thermal analysis (TGA/DSC), scanning electron microscopy (SEM) and low temperature adsorption–desorption of nitrogen (BET method). The synthesized powders consisted of porous plate-like particles with micrometer dimensions. Specific surface area calculated by the BET method was found to be 7 m2 g−1. For the estimation of sorption properties, the aqueous model solutions containing different metal ions (Al3+, Cd2+, Co2+, Cu2+, Fe2+, Mn2+, Ni2+, Pb2+, Sn2+, Sr2+ and Zn2+) were used. The adsorption test revealed that β-Ca2P2O7 demonstrates the highest adsorption capacity for Pb2+ and Sn2+ ions, while the lowest capacity was observed towards Sr2+, Ni2+ and Co2+ ions. The optimal pH value for the removal of Pb2+ ions was determined to be 2, which is also related to the low solubility of β-Ca2P2O7 at this pH. The adsorption capacity towards Pb2+ ions was calculated as high as 120 mg g−1.