Large-Scale Production of Rectorite Nanosheets and Their Co-Assembly with Aramid Nanofibers for High-Performance Electrical Insulating Nanopapers.

Compared with raw rectorite microplatelets (RMs), rectorite nanosheets (RNs) have considerably greater application prospects in the preparation of advanced composite materials because of their larger aspect ratio, higher surface reactivity, and intrinsically superior mechanical and physical properties. However, the difficulty in the efficient preparation of RNs significantly limits their large-scale applications. Here, a scalable poly(vinylpyrrolidone)-assisted stirring approach is developed to prepare ultrathin RNs from the abundant natural RMs. A higher production rate (≈0.675 g h-1 ) is achieved compared with that of most other nanosheets. Additionally, instead of using conventional time- and energy-consuming high-speed centrifugation, an efficient poly(dienedimethylammonium chloride)-assisted sedimentation strategy is proposed here to rapidly separate the exfoliated RNs from the RN dispersion. Then, the RNs are co-assembled with aramid nanofibers (ANFs) into large-scale nacre-mimetic ANF-RN nanopapers with considerably enhanced mechanical, electrical insulating, and high-temperature-resistant properties compared with pure ANF nanopapers and ANF-RM micropapers. Moreover, these properties are superior to those of previously reported ANF-based nanopapers and commercial insulating micropapers.

Clean synthesis of RGO/Mn3O4 nanocomposite with well-dispersed Pd nanoparticles as a high-performance catalyst for hydroquinone oxidation.

In this study, a well-dispersed Pd nanoparticle (NP)-supported RGO/Mn3O4 (G/M/Pd) composite was synthesized by a clean synthetic route, where galvanic replacement reaction simply occurred between Mn3O4 and a palladium salt, thereby avoiding the use of harsh reducing and capping agents. The G/M/Pd composite served as a robust catalyst for the catalytic oxidation of hydroquinone (HQ) to benzoquinone (BQ) with H2O2 in an aqueous solution. Oxidation was completed in only 4 min, with a turnover frequency (TOF) of 3613 h-1; this TOF is one hundred times those of previously reported Pd- and Ag-based catalysts. The superior performance was related to the electronic inductive effect between Mn3O4 and Pd NPs, which was verified by density functional theory calculations. Trapping experiments revealed that the oxidation of HQ was considerably related to the ·OH radicals generated from the decomposition of H2O2. In addition, the influencing factors were further investigated, including catalyst and HQ concentrations, solution pH, solvents, and various inorganic and organic interferences. Moreover, the G/M/Pd catalyst exhibits diverse applications for the catalytic oxidation of HQ derivatives with high TOFs.