RESUMO
γ-Fe2O3/C nanocomposite was prepared through a convenient method by which one-pot synthesized Fe3O4/Starch was oxidized and carbonized by calcining at 250 °C. The γ-Fe2O3/C displayed strong magnetism and could adsorb organic molecules from aqueous solution effectively, thus it showed promising application in the dislodgement of organic pollutants in sewage. Adsorption isotherms and kinetics of methylene blue (MB) onto γ-Fe2O3/C were studied in a batch system. The adsorption process reached equilibrium in about 15 min, and the maximum adsorption capacity of MB was found to be 64.9 mg g-1 at 303 K. Adsorption isotherms were well fitted to Langmuir model and the adsorption kinetics could be described by the pseudo-second order kinetic equation. The findings of the present work highlight a new facile method to fabricate magnetic carbon-based composites and the obtained γ-Fe2O3/C with excellent magnetic property and adsorption performance hold great promise for practical application in water treatment.
RESUMO
We utilized a novel strategy, hierarchical structuring, to enhance the catalytic activity of coordination polymers. Hierarchical Prussian white crystals with hollow structures and kinked surfaces were synthesized by using a self-aggregation and etching strategy. The hierarchical structure significantly enhanced the catalytic activity of Prussian white in the degradation of methylene blue in comparison to the non-hierarchical Prussian white crystals.
RESUMO
Core-shell structured Fe3O4@C nanoparticles were fabricated by a facile one-pot hydrothermal route. The structure and component of the nanoparticles were fully characterized by transmission electron microscopy, X-ray diffraction, Mössbauer spectroscopy, Raman spectroscopy, thermogravimetric analysis, magnetometry and Brunauer-Emmett-Teller specific surface area measurements. The obtained Fe3O4@C nanoparticles possessed favorable dispersibility, high saturation magnetization (61.4 emu g-1) that could quickly respond to external magnetic field and excellent biocompatibility. Excitingly, the experiments of the Fe3O4@C nanoparticles as drug carriers revealed an efficient drug-loading as high as 1.08 mg mg-1. More importantly, the drug loading composite exhibited pH-responsive release profiles and the duration was as long as 200 h; at the pH value of 5.8 and 7.4, the release rate was 93.7% and 33.6%, respectively. Furthermore, the obtained Fe3O4@C nanoparticles had good magneto-thermal ability. All these positive attributes make the as-prepared Fe3O4@C nanoparticles a promising platform for further biomedical evaluations.
RESUMO
In the title compound, C(6)H(7)IN(2), the non-H atoms of the mol-ecule are located on a crystallographic mirror plane; the H atoms of the methyl groups are therefore disordered over two positions of equal occupancy. In the crystal structure, short inter-molecular Iâ¯N contacts [3.390â (3)â Å] are found, linking the mol-ecules into zigzag chains. In addition, there are inter-molecular π-π stacking inter-actions between the pyrimidine rings of adjacent mol-ecules [centroid-centroid distance = 3.5168â (10)â Å], resulting in a two-dimensional supra-molecular architecture.