In situanchoring of Fe3O4/CNTs hybrids on basalt fiber for efficient electromagnetic wave absorption.

The development of practical and efficient electromagnetic wave (EMW) absorbing materials is a challenging research problem. A mussel-inspired molecular structure regulation strategy using polydopamine to increase the roughness and functional groups of basalt fiber (BF) surface, which can improve the fiber interfacial adhesion. Herein, a novel BF-Fe3O4/CNTs heterostructure is synthesized through a dip-coating adsorption process. The three-dimensional network structure of Fe3O4/CNTs hybridin situanchored on the surface of BF, which endows the composite to have good intrinsic magnetic and dielectric properties. Modulation of EMW absorption performance by controlling the addition of CNTs, the minimum RL of BF-Fe3O4/7C reaches to -40.57 dB at a thickness of 1.5 mm with CNTs addition of 7%. The enhanced EMW absorption performance of BF-Fe3O4/7C heterostructure may be attributed to the synergistic effects of interfacial polarization between the hollow magnetic Fe3O4spheres and CNTs, conduction loss, magnetic resonance loss and multiple reflection/scattering inside the BF. This work provides a simple pathway to design EMW absorbing materials with good environmental stability.

Prediction and measurement of the electromagnetic environment of high-power medium-wave and short-wave broadcast antennas in far field.

With the increasing city size, high-power electromagnetic radiation devices such as high-power medium-wave (MW) and short-wave (SW) antennas have been inevitably getting closer and closer to buildings, which resulted in the pollution of indoor electromagnetic radiation becoming worsened. To avoid such radiation exceeding the exposure limits by national standards, it is necessary to predict and survey the electromagnetic radiation by MW and SW antennas before constructing the buildings. In this paper, a modified prediction method for the far-field electromagnetic radiation is proposed and successfully applied to predict the electromagnetic environment of an area close to a group of typical high-power MW and SW wave antennas. Different from currently used simplified prediction method defined in the Radiation Protection Management Guidelines (H J/T 10. 3-1996), the new method in this article makes use of more information such as antennas' patterns to predict the electromagnetic environment. Therefore, it improves the prediction accuracy significantly by the new feature of resolution at different directions. At the end of this article, a comparison between the prediction data and the measured results is given to demonstrate the effectiveness of the proposed new method.

[Preparation, characterization and upconversion fluorescence of NaYF4 : Yb, Er /graphene oxide nanocomposites].

NaYF4 : Yb, Er/rGO and SiO2-coated NaYF4 : Yb, Er/rGO nanocomposites can be prepared through "one-pot" and directly mixing preparation routes. Various measurement results show that the NaYF4 : Yb, Er in the nanocomposites exhibits a cubic a-type structure and nanoparticle-like morphology with a diameter range of 30-70 nm; the rGO layers are well-dispersed in the nanocomposites, and whereas the rGO obtained from "one-pot" preparation renders relatively better dispersion. Raman spectra demonstrate that there exists a surface coupling action between the two kinds of nanomaterials, and with the increase in the relative rGO content, such action becomes stronger. UC fluorescence measurement results reveal that the rGO has significantly quenching effect and optical-limiting performance on the UC fluorescence, particularly on the red-emission of the NaYFa : Yb, Er or SiO2-coated NaYF4 : Yb, Er nanoparticles. The red-emission intensity gradually decreases with an increase in the rGO content, but the green-emission shows less change. It should be stressed that, in comparison with NaYF4 : Yb, Er/rGO, with a similar rGO content, the red-emission intensity of SiO2-coated NaYF4 : Yb, Er/rGO decreases much obviously due to a stronger light-absorption caused by part rGO aggregation.