Search

In this paper, we report a microwave-assisted biosynthesis method with Cinnamomum camphora (CC) leaf extract for the green and rapid synthesis of Ag nanoparticles (NPs). The as-produced Ag nanoparticles were immobilized onto CeO 2 as supported Ag/CeO 2 catalyst, which proved to be efficient for carbon monoxide (CO) oxidation. Active components in the plant extract were identified by FTIR analysis and later on validated through simulated experiments. The results revealed that polyphenols and proteins were the reducing and protecting agents, respectively. The optimum preparation conditions for the catalyst were irradiation time of 140 s, Ag loadings of 5 wt.%, CC extract concentration of 25 g L −1 and sintering temperature of 300 °C. Since biomolecules adsorbed over the surface of catalyst was detrimental to its catalytic activity, calcination to remove the biomolecules was critical to the enhanced activity. Considering the trade-off between particle size and biomass removal extent, the optimum calcination temperature was determined to be 300 °C.

Au/TS-1 catalysts prepared by an eco-friendly and economical bioreduction method were used for the liquid phase epoxidation of styrene to styrene oxide (SO) using aqueous hydrogen peroxide (H2O2) as oxidant. The catalysts were characterized by a variety of techniques including FT-IR, DRUV–Vis, UV–Vis, N2 physisorption, XRD, XPS, TG–DTG and TEM. The influence of various parameters (Au loading, calcination, solvents, oxidants, reaction temperature, reaction time and catalyst amount) on the catalytic performance was systematically investigated. The results showed that both the conversion of styrene and selectivity to SO were improved and enhanced when catalyzed by biosynthesized gold nanoparticles (GNPs) supported on TS-1. However, decomposing the Cacumen Platycladi (CP) biomass properly through calcinations can enhance the catalytic performance though it acted as reductant and protective agents during the catalysts preparation. Besides, the optimum catalytic activity and stability of bioreduction Au/TS-1 catalysts were obtained under operational conditions of Au loading of 1.0 wt.%, CP extract (10 g L−1) as reductant, calcined at 723 K for 2 h, reaction time of 10 h, reaction temperature of 333 K, catalyst amount of 500 mg, aqueous H2O2 (30 wt.%) as oxidant and N,N-dimethylformamide as solvent. Under the optimal condition, styrene conversion of 92.7% and SO selectivity of 90.4% was achieved, which were comparable or even superior to those reported in the literatures. The catalyst was reused five times, without significant decrease in both the styrene conversion and SO selectivity.