Silicon carbide (SiC) was modified by melamine polyphosphate (MPP)-modified silicone to form SiC-MPP, then incorporated into epoxy resin (EP) for developing thermally resistant composites, which showed thermal conductivity and flame retardancy performance. The EP/SiC-MPP composites were prepared by blending and cured under 60°C for 2 h and 150°C for 8 h. The grafting degree of SiC-MPP was analyzed using Fourier transform Infrared, scanning electron microscope, and thermogravimetric measurements. The flame retardancy of the EP/SiC-MPP composites was studied by UL-94 vertical combustion and cone calorimetry test. The results showed that for EP/SiC-MPP containing 20 wt%, the UL-94 was case V1. Also compared to pure epoxy, the peak heat release rate (PHRR) of composites was reduced from 800 to 304 kW·m−2. The thermal conductivity of EP/SiC-M20 composites was 0.53 W·m−1·K−1, almost 2.5-fold higher than pure epoxy (0.21 W·m−1·K−1). The as-prepared EP/SiC-MPP composites exhibited enhanced flame retardancy and thermal conductivity. Based on analyses performed, these composites took credit-related applications.
Two new trinuclear zinc(II) complexes, [Zn3I2L2(H2O)2] (1) and [Zn3(CH3OH)(DMF)L2(NCS)2] (2), where L is the dianionic form of N,N’-bis(5-bromosalicylidene)-1,2-cyclohexanediamine (H2L), have been synthesized and characterized by elemental analyses, IR and UV spectra. Structures of the complexes were further confirmed by single crystal X-ray diffraction. Both complexes are trinuclear zinc compounds. Both compounds are solvated, with water ligand for 1 and methanol ligand for 2. The outer two Zn atoms are in square pyramidal coordination, while the inner one is in octahedral coordination. The effect of the complexes on the antimicrobial activity against Staphylococcus aureus, Escherichia coli and Candida albicans were evaluated, and gave interesting results.
A process simulation model and a statistical method comprising full factorial and response surface designs were employed to study and optimize acrylamide polymerization in a batch reactor. It was evaluated that the dependence of factors such as initial mass fractions of initiator and acrylamide, reacting temperature and operation time in affecting the polymer weight-average (Mw) of polyacrylamide and acrylamide conversion. The simulation model was established on the basis of a kinetic mechanism that refers to backbiting, termination by disproportionation and combination, as well as gel effect, to achieve the Mw of polyacrylamide and acrylamide conversion. Full factorial and response surface designs were developed to screen significant factors and to build reliable predictive function models for polyacrylamide Mw and acrylamide conversion. The results showed significant independent and interactive factor effects on polyacrylamide Mw and acrylamide conversion and were used to optimize the polymerization of acrylamide.
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