Organic/inorganic nanocomposite polymer electrolyte

The organic/inorganic nanocomposites polymer electrolytes were designed and synthesized. The organic/inorganic nanocomposites membrane materials and their lithium salt complexes have been found thermally stable below 200 °C. The conductivity of the organic/inorganic nanocomposites polymer electrolytes prepared at room temperature was at magnitude range of 10(?6) S/cm.

Boron Oxide Glasses and Nanocomposites: Synthetic, Structural and Statistical Approach

Three different precursors of boron-aqua and glycerol solutions of boric acid and ethanol solution of trimethyl borate were used for the preparation of organic–inorganic advanced materials. The films and bulk materials samples were heat treated at 100, 400, 800？C for 2 h. The hybrid samples were stable and transparent until 100？C. The further increase of temperature to 400？C led to destruction of samples, and at 800？C they were molten. The structural changes during the pyrolysis were studied by Fourier transform infrared spectroscopy, differential thermal analysis, and X-ray diffraction. Details of surface morphology were observed by scanning electron microscopy. The obtained BO_3 and BO_4 groups were identified in the molten materials after pyrolysis. The quantities and order of borate structural units as well as residual carbon in the networks depended on boron precursor type. PVA/PEG/B_2O_3 hybrid materials were proved to be appropriate precursors for synthesizing borate and carboborate glass and carbon/borate glass nanocomposites. To access the impact of the experimental conditions on the structural changes of the nanocomposites, cluster analysis of the IR-spectral data was used as a classification method.

A nanoconcrete welding strategy for constructing high-performance wound dressing

Engineering biomaterials to meet specific biomedical applications raises high requirements of mechanical performances,and simultaneous strengthening and toughening of polymer are frequently necessary but very challenging in many cases.In this work,we propose a new concept of nanoconcrete welding polymer chains,where mesoporous CaCO3(mCaCO_(3))nanoconcretes which are composed of amorphous and nanocrystalline phases are developed to powerfully weld polymer chains through siphoning-induced occlusion,hydration-driven crystallization and dehydration-driven compression of nanoconcretes.The mCaCO_(3) nanoconcrete welding technology is verified to be able to remarkably augment strength,toughness and anti-fatigue performances of a model polymer poly(3-hydroxybutyrate-co-3-hydroxyvalerate)-based porous membrane.Mechanistically,we have revealed polymer-occluded nanocrystal structure and welding-derived microstress which is much stronger than interfacial Van der Waals force,thus efficiently preventing the generation of microcracks and repairing initial microcracks by microcracks-induced hydration,crystallization and polymer welding of mCaCO_(3) nanoconcretes.Constructed porous membrane is used as wound dressing,exhibiting a special nanoplates-constructed surface topography as well as a porous structure with plentiful oriented,aligned and opened pore channels,improved hydrophilicity,water vapor permeability,anti-bacterial and cell adherence,in support of wound healing and skin structural/functional repairing.The proposed nanoconcrete-welding-polymer strategy breaks a new pathway for improving the mechanical performances of polymers.