No abstract

No abstract

Three-dimensional (3D) macro-mesoporous structures demonstrate effective performance for gas sensing. In this work, we have designed and successfully prepared aperture-controllable three-dimensional interconnected macro-mesoporous ZnO (3D-IMM-ZnO) nanostructures by template-based layer-by-layer filtration deposition. XRD, SEM, and TEM have been used to characterize the obtained hexagonal wurzite 3D-IMM-ZnO nanostructures. Owing to its special 3D interconnected hierarchically porous structure, the 3D-IMM-ZnO nanostructures exhibit excellent gas sensing performances toward acetone and methanol. The 3D-IMM-ZnO nanostructure with the largest macropore demonstrates the best gas sensitivity owing to its largest cavity providing enough space for gas diffusion. On the basis of the results and analyses, we propose that the synergistic effect of electron liberation and electron density of acetone and the special structure make the 3D-IMM-ZnO nanostructures demonstrate better gas sensing properties than many other porous ZnO nanostructures and preferred selectivity to acetone.

Carboxymethyl chitosan (CMCS) microparticles are a potential candidate for hemostatic wound dressing. However, its low swelling property limits its hemostatic performance. Poly(γ-glutamic acid) (PGA) is a natural polymer with excellent hydrophilicity. In the current study, a novel CMCS/PGA composite microparticles with a dual-network structure was prepared by the emulsification/internal gelation method. The structure and thermal stability of the composite were determined by Fourier transform infrared spectroscopy (FTIR), X-ray powder diffraction (XRD), scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis (TGA). The effects of preparation conditions on the swelling behavior of the composite were investigated. The results indicate that the swelling property of CMCS/PGA composite microparticles is pH sensitive. Levofloxacin (LFX) was immobilized in the composite microparticles as a model drug to evaluate the drug delivery performance of the composite. The release kinetics of LFX from the composite microparticles with different structures was determined. The results suggest that the CMCS/PGA composite microparticles are an excellent candidate carrier for drug delivery.

No abstract