Biphasic calcium phosphate (BCP) is a bioceramic widely used in hard tissue engineering for bone replacement. BCP consists of β-tricalcium phosphate (β-TCP) - a highly soluble and resorbable phase - and hydroxyapatite (HA) - a highly stable phase, creating a balance between solubility and resorption, optimally supporting cell interactions and tissue growth. The β-TCP/HA ratio significantly affects the resorption, solubility, and cellular response, with a higher β-TCP ratio increasing resorption due to its solubility. BCP is commonly synthesized by calcining calcium-deficient apatite (CDA) at temperatures above 700 °C via direct or indirect methods. This study investigated the effects of pH and sintering temperature on BCP synthesized via wet precipitation, aiming to achieve an 80/20 β-TCP/HA ratio, which is known to be optimal for bone regeneration. By maintaining a constant Ca/P precursor ratio of 1.533, the optimal conditions were determined to be a pH of 5.5-6 and a sintering temperature of 900 °C, chosen to balance material stability and solubility. The successful synthesis was confirmed using X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy. At the same time, the material's physical and chemical properties were further characterized through scanning electron microscopy (SEM) and degradation studies in a simulated body fluid (SBF). In vitro tests demonstrated excellent cytocompatibility and osteogenic differentiation, while in vivo studies on rabbit femur defects demonstrated significant bone regeneration, with bone-to-tissue volume ratios exceeding 50% within four weeks. These results highlight the potential of BCPs in bone tissue engineering and biomaterials research.
Onion-like carbon nano particles are separated from diesel engine exhaust “pollutant soot” and used in the structural health monitoring of a biocomposite.
Covalent organic frameworks are porous crystals of polymers with two categories based on their covalent linkages: layered structures with two dimensions and networks with three-dimensional structures. Three-dimensional covalent organic frameworks are porous, have large surface areas, and have highly ordered structures. Since covalent bonds are responsible for the formation of three-dimensional covalent organic frameworks, their synthesis has been a challenge and different structures are generated during the synthesis. Moreover, initially, their topologies have been limited to dia, ctn, and bor which are formed by the condensation of triangular or linear units with tetrahedral units. There are very few building units available for their synthesis. Finally, the future perspective of 3D COFs has been designated for the future development of three-dimensional covalent organic frameworks.
A graphene oxide@BiBTC MOF photocatalyst was prepared by in situ using a hydrothermal method. The as-prepared composite was applied in five cycles for RhB with 90% photodegrading efficiency.
Rapid recombination of charge carriers in semiconductors is a main drawback for photocatalytic oxidative coupling of methane (OCM) reactions. Herein, we propose a novel catalyst by developing a p–n junction titania–silicon nanowires (TiO 2 /SiNWs) heterostructure. The structure is fabricated by atomic layer deposition of TiO 2 on p-type SiNWs. The TiO 2 /SiNWs heterostructure exhibited an outstanding OCM performance under simulated solar light irradiation compared to the single components. This enhanced efficiency was attributed to the intrinsic electrical field formed between n-type TiO 2 and p-type SiNWs, which forces generated charge carriers to move in opposite directions and suppresses charge recombination. Besides, surface morphology and optical properties of the the p–n TiO 2 /SiNWs catalyst are also beneficial for the photocatalytic activity. It is expected that the results of this study will provide massive guidance in synthesizing an efficient photocatalyst for CH 4 conversion under mild conditions.