Fluorine and Bromine Dual-Doped Nanoporous Carbons: Preparation and Surface Chemistry Studies.

A novel method for the concurrent introduction of fluorine and bromine into the surface of nanoporous activated carbon (NAC) is evaluated. According to the method, the preheated NAC was treated with 1,2-dibromotetrafluoroethane at elevated temperatures (400-800 °C). Potentiometric and elemental analysis, nitrogen adsorption-desorption, scanning electron microscopy-energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy (XPS), and F solid-state NMR were used to study the NAC microstructure and changes in surface chemistry.

Surface chemistry and catalytic activity in HO decomposition of pyrolytically fluoralkylated activated carbons.

According to the proposed pyrolytic method, granular activated carbon (AC) Norit 830 W was functionalized by thermal treatment of AC in hydrofluorocarbon (HFC) gases, pentafluoroethane and 1,1,1,2-tetrafluoroethane, at 400-800 °C. This method does not require activation by plasma and photons. Chemical and elemental analysis showed that the pyrolytic treatment provides a loading of 2.

NiFe and CoFe nanocatalysts supported on highly dispersed alumina-silica: Structure, surface properties, and performance in CO methanation.

The hydrogenation of CO to CH has gained considerable interest in terms of sustainable energy and environmental mitigation. In this regard, the present work aims to investigate the adsorptive concentration and CO methanation performance over CoFe and NiFe bimetallic catalysts supported on fumed alumina-silica SA96 support at 170-450 °C and under atmospheric pressure. The catalysts were prepared by wet impregnation method, subjected to calcination and further reduced with hydrogen, and their performance in CO methanation was investigated in a hydrogen-rich 2%CO-55%H-43%He gas mixture.

Development of a Crystallization-Induced Diastereomer Transformation of Oxime Isomers for the Asymmetric Synthesis of (1,6)-3,9-Diazabicyclo[4.2.1]nonane.

Herein we report a practical crystallization-induced diastereomer transformation (CIDT) of oxime isomers for the scalable asymmetric synthesis of the bicyclic diamine (1,6)-3,9-diazabicyclo[4.2.1]nonane derivative that serves as a valuable building block in medicinal chemistry.

Photo- and Radiofrequency-Induced Heating of Photoluminescent Colloidal Carbon Dots.

Nitrogen- and oxygen-containing carbon nanoparticles (O, N-CDs) were prepared by a facile one-step solvothermal method using urea and citric acid precursors. This method is cost-effective and easily scalable, and the resulting O, N-CDs can be used without additional functionalization and sample pretreatment. The structure of O, N-CDs was characterized by TEM, AFM, Raman, UV-vis, and FTIR spectroscopies.