Co-doped MoS 2 nanosheets have been synthesized through the hydrothermal reaction of ammonium tetrathiomolybdate and hydrazine in the presence of cobalt acetate. These nanosheets exhibit a dominant metallic 1T phase with cobalt ion-activated defective basal planes and S-edges. In addition, the nanosheets are dispersible in polar solvents like water and methanol. With increased active sites, Co-doped MoS 2 nanosheets exhibit exceptional catalytic activity in the reduction of nitroarenes by NaBH 4 with impressive turnover frequencies of 8.4, 3.2, and 20.2 min –1 for 4-nitrophenol, 4-nitroaniline, and nitrobenzene, respectively. The catalyst is magnetic, enabling its easy separation from the reaction mixture, thus making its recycling and reusability simple and efficient. The enhanced catalytic activity of the Co-doped 1T MoS 2 nanosheets in comparison to that of undoped 1T MoS 2 nanosheets suggests that incorporation of cobalt ions in the MoS 2 lattice is the major reason for the efficiency of the catalyst. The dopant, Co, plays a dual role. In addition to providing active sites where electron transfer is assisted through redox cycling, it renders the nanosheets magnetic, enabling their easy removal from the reaction mixture.
Three types of polyhedral oligomeric silsesquioxane (POSS)—octaphenyl (OP), POSS@TESPT (TT), and MWCNT@POSS (VC)—were incorporated into natural rubber (NR) to fabricate nanocomposites. The transport properties of POSS–NR nanocomposites were studied through solvent diffusion techniques. Diffusion studies were done with toluene (aromatic solvent) and the influence of nanofiller structure, concentration and compatibility with the NR matrix on various diffusion parameters were analyzed. The fillers that have good interaction with the polymer matrix showed the lowest solvent uptake. The network structure analysis revealed that the polymer chains deformed affinely. The effect of fillers on the chain flexibility was also discussed based on mechanical property studies. POLYM. COMPOS., 40:3020–3031, 2019. © 2018 Society of Plastics Engineers
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