Controllable Preparation of Fe3O4@RF and Its Evolution to Yolk–Shell-Structured Fe@C Composite Microspheres with High Microwave Absorbing Performance

Fe3O4@RF microspheres with different phenolic (RF) layer thicknesses are prepared by adjusting the polymerization time. With the prepared Fe3O4@RF as the precursor, Fe@C composite microspheres with rattle-like morphology are obtained through one-step controlled carbonization. This method simplifies the preparation of rattle-shaped microspheres from sandwich microspheres. Fe@C microspheres exhibit excellent microwave absorbing properties. The morphology and composition of the product are investigated depending on the effects of carbonization temperature, time and thickness of the RF layer. When the carbonization temperature is 700 °C, the carbonization time is 12 h and the polymer shell thickness is 62 nm, the inner hollow Fe3O4 is completely reduced to Fe. The absorption properties of the materials are compared before and after the reduction of Fe3O4. Both Fe@C-12 and Fe3O4@C-700 show excellent absorbing properties. When the filler content is 50%, the maximum reflection loss (RLmax) of the rattle-shaped Fe@C microspheres is −50.15 dB, and the corresponding matching thickness is 3.5 mm. At a thickness of 1.7 mm, the RLmax of Fe3O4@C-700 is −44.42 dB, which is slightly worse than that of Fe@C-12. Both dielectric loss and magnetic loss play a vital role in electromagnetic wave absorption. This work prepares rattle-shaped absorbing materials in a simple way, which has significance for guiding the construction of rattle-shaped materials.

EFFICIENT ADSORPTION OF Ce (III) ONTO POROUS CELLULOSE/GRAPHENE OXIDE COMPOSITE MICROSPHERES PREPARED IN IONIC LIQUID

A novel adsorbent made of porous cellulose/graphene oxide composite microspheres (PCGCM) was synthesized in [Bmim]Cl ionic liquid. The as-prepared PCGCM was evaluated for the removal of Ce (III) via static adsorption experiments. The results showed that the adsorption equilibrium of Ce (III) onto PCGCM was achieved within 50 min and the adsorption was highly pH dependent. An excellent adsorption capacity as high as 415.1 mg•g-1 was obtained at a pH of 4.9, which was much higher than most adsorbents reported in the literature. The pseudo-second order kinetic model and Langmuir isotherm model were found to fit the adsorption behavior of PCGCM well. The XPS analysis confirmed that the adsorption was based on the ion exchange mechanism. Meanwhile, PCGCM could be regenerated with 1 mol•L-1 HCl for repetitious adsorption of Ce (III). This work provides an attractive approach for the removal of rare earth ions as pollutants.