Hierarchically porous 3D-printed akermanite scaffolds from silicones and engineered fillers

The present investigation is dedicated to the manufacturing of reticulated three-dimensional akermanite scaffolds, developed by direct reaction between silica, from the oxidation of a commercial silicone resin and oxide fillers, forming pastes for direct ink writing. Crack-free scaffolds, with dense and regular struts, were due to the use of CaCO3 (micro) and MgO nano-particles as reactive fillers. An excellent phase purity was obtained, with the help of the liquid phase provided by anhydrous sodium borate (Na2B4O7), upon firing. The structure of the scaffolds, finally, was successfully modified by using Mg(OH)2 and hydrated sodium borate: besides macro-porosity from direct ink writing, the new scaffolds exhibited homogenous \u2018spongy\u2019 struts (owing to water vapor release in the heating step), with no crack. Both types of scaffolds (with dense or porous struts) exhibited remarkable strength-to-density ratios

Crystallization and visible-near-infrared luminescence of Bi-doped gehlenite glass

Gehlenite glass microspheres, doped with a different concentration of Bi3+ ions (0.5, 1, 3 mol%), were prepared by a combination of solid-state reaction followed by flame synthesis. The prepared glass microspheres were characterized from the point of view of surface morphology, phase composition, thermal and photoluminescence (PL) properties by optical and scanning electron microscopy (SEM), X-ray diffraction (XRD), differential scanning calorimetry (DSC) and PL spectroscopy. The closer inspection of glass microsphere surface by SEM confirmed a smooth surface. This was further verified by XRD. The basic thermal characteristics of prepared glasses, i.e. Tg (glass transition temperature), Tx (onset of crystallization peak temperature), Tf (temperature of the inflection point of the crystallization peak) and Tp (maximum of crystallization peak temperature), were estimated from the DSC records. High-temperature XRD experiments in the temperature interval range 600–1100°C were also performed. The PL emission properties of prepared glasses and their polycrystalline analogues (glass crystallized at 1000°C for 10 h) were studied in the visible and near-infrared (NIR) spectral range. When excited at 300 nm, the glasses, as well as their polycrystalline analogues, exhibit broad emission in the visible spectral range from 350 to 650 nm centred at about 410–450 nm, corresponding to Bi3+ luminescence centres. The emission intensity of polycrystalline samples was found to be at least 30 times higher than the emission of their glass analogues. In addition, a weak emission band was observed around 775 nm under 300 nm excitation. This band was attributed to the presence of a minor amount of Bi2+ species in prepared samples. In the NIR spectral range, the broad band emission was observed in the spectral range of 1200–1600 nm with the maxima at 1350 nm. The chemistry of Bi and its oxidation state equilibrium in glasses and polycrystalline matrices is discussed in detail

Glass powders and reactive silicone binder: Interactions and application to additive manufacturing of bioactive glass-ceramic scaffolds

A novel concept for the additive manufacturing of three-dimensional glass-ceramic scaffolds, to be used for tissue engineering applications, was based on fine glass powders mixed with a reactive binder, in the form of a commercial silicone. The powders consisted of ‘silica-defective glass’ specifically designed to react, upon firing in air, with the amorphous silica yielded by the binder. By silica incorporation, the glass was intended to reach the composition of an already known CaONa2OB2O3SiO2 system. Silica from the binder provided up to 15 wt% of the total silica. With the same overall formulation, silicone-glass powder mixtures led to nearly the same phase assemblage formed by the reference system, crystallizing into wollastonite (CaSiO3) and Ca-borate (CaB2O4). Samples from silicone-glass powder mixtures exhibited an excellent shape retention after firing, which was later exploited in highly porous reticulated scaffolds, obtained by means of direct ink writing (DIW)

Magnetic properties of yttrium iron garnet polycrystalline material prepared by spray-drying synthesis

The yttrium iron garnet polycrystalline powder was prepared by spry-drying synthesis from nitrates solution. The calcined powder was pressed into pellets and sintered at various temperatures for 2 hours. Prepared samples were characterized by XRD analysis and magnetic properties were measured. The magnetic moment of 4.3 µB and saturation magnetization of 24 Am2kg-1were observed for sample sintered at 1000 °C

Low-alkali borosilicate glass microspheres from waste cullet prepared by flame synthesis

Although glass recycling is considered to be a default method for glass waste management, fine fractions of container soda-lime glass, or cullet of other compositions are still landfilled. This happens despite existing alternatives. Success could lie in advanced upcycled products that bring higher economic motivation for the implementation in industry, but these are often connected to alternative ways of product synthesis. We provide an example of waste glass upcycling by the preparation of glass microspheres (GM) from specialty low-sodium alumino borosilicate-based glasses via flame synthesis (FS). GM and the precursors, either from colorless medical vials or glass fibers, were characterized by scanning electron microscopy (SEM), simultaneous thermal analysis coupled with differential thermal analysis (STA-DTA), and image analysis. A dynamic corrosion test was performed and evaluated via ion-coupled plasma with optical emission spectroscopy (ICP-OES) to observe corrosion kinetics products. FS has proved to be a fast method of waste glass processing into GM. This article, besides the characterization of the starting material and final products, also suggests the possibility of processing for other landfilled waste glasses and also discusses the manufacturing of GM for water filters and fillers for polymers