In this research, using hexaphenoxycyclotriphosphazene (HPCTP) as the halogen-free flame retardant, we prepared flameretardant expandable polystyrene (EPS) beads by suspension polymerization. The effects of process parameters and the amount of flame retardant on polystyrene (PS)/HPCTP composite beads were investigated. The results show that the change in HPCTP content has little effect on the particle size distribution of composite beads. When the oil-water ratio is 1/4, TCP dosage is 3 wt %, stirring rate is 350 rpm, initiator dosage is 1.25 wt %, and HPCTP dosage is 15 wt %, the size of the composite beads is uniform, and the average particle size is 1.12 mm. HPCTP formed nanodispersed particles in the PS matrix with an average particle size of 44.86 nm. In addition, the thermogravimetric behavior and heat-release properties of composite beads were evaluated. The results showed that HPCTP mainly acted in the gaseous phase, which can effectively decrease the maximum mass-loss rate of the PS/HPTCP composite beads and significantly reduce the heat-release rate and heat-release capacity. The EPS foams were obtained by a prefoaming method. The average cell diameter was 62.15 μm, and the foaming ratio was 11 times.
Bioprinting is an attractive technology for building tissues from scratch to explore entire new cell configurations, which brings numerous opportunities for biochemical research such as engineering tissues for therapeutic tissue repair or drug screening. However, bioprinting is faced with the limited number of suitable bioinks that enable bioprinting with excellent printability, high structural fidelity, physiological stability, and good biocompatibility, particularly in the case of extrusion-based bioprinting. Herein, we demonstrate a composite bioink based on gelatin, bacterial cellulose (BC), and microbial transglutaminase (mTG enzyme) with outstanding printing controllability and durable architectural integrity. BC, as a rheology modifier and mechanical enhancer component, endows the bioink with shear-thinning behavior. Moreover, the printed structure becomes robust under physiological conditions owing to the in situ chemical crosslinking catalyzed by mTG enzyme. Lattice, bowl, meniscus, and ear structures are printed to demonstrate the printing feasibility of such a composite bioink. Furthermore, the 3D-printed cell-laden constructs are proved to be a conducive biochemical environment that supports growth and proliferation of the encapsulated cells in vitro. In addition, the in vivo studies convince that the composite bioink possesses excellent biocompatibility and biodegradation. It is believed that the innovation of this new composite bioink will push forward the bioprinting technology onto a new stage.
Materials with the formula Yb 2−x AlxMo 3 O 12 (x = 0.1, 0.2, 0.3, 0.4, 0.5, 0.7, 0.9, 1.0, 1.1, 1.3, 1.5, and 1.8) were synthesized and their structures, phase transitions, and hygroscopicity investigated using X-ray powder diffraction, Raman spectroscopy, and thermal analysis. It is shown that Yb 2−x AlxMo 3 O 12 solid solutions crystallize in a single monoclinic phase for 1.7 ≤ x ≤ 2.0 and in a single orthorhombic phase for 0.0 ≤ x ≤ 0.4, and exhibit the characteristics of both monoclinic and orthorhombic structures outside these compositional ranges. The monoclinic to orthorhombic phase transition temperature of Al 2 Mo 3 O 12 can be reduced by partial substitution of Al 3+ by Yb 3+ , and the Yb 2−x AlxMo 3 O 12 (0.0 < x ≤ 2.0) materials are hydrated at room temperature and contain two kinds of water species. One of these interacts strongly with and hinders the motions of the polyhedra, while the other does not. The partial substitution of Al 3+ for Yb 3+ in Yb 2 Mo 3 O 12 decreases its hygroscopicity, and the linear thermal expansion coefficients after complete removal of water species are measured to be
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