Abstract
Pinewood biochar (PBC)-supported metallic silver (Ago) was prepared via a one-step carbothermal reduction route (AgH) or a wet-chemistry reduction method (AgW). XRD and SEM confirmed Ago was soldered on PBC matrix. Low methylene blue (MB) sorption was observed for unsupported Ago nanoparticles (AgNP), AgH and AgW. Under ultraviolet (UV) light irradiation, net MB degradation by AgH (15.88 g kg−1) was higher than that of AgW (12.50 g kg−1) and AgNP (10.27 g kg−1). TOC removal percentages after degradation corresponded largely to reduction of MB concentrations in solution, indicating MB was dominantly mineralized. Electron paramagnetic resonance (EPR) revealed that MB was degraded by reactive oxygen species (ROS) such as hydroxyl radical (OH), superoxide radical (O2-) and singlet oxygen (1O2). The scavenging experiments further suggested that OH scavengers suppressed MB degradation to a greater extent than other quenchers. Compared to AgW, AgH possessed greater abundance of persistent free radicals, which enhance ROS generation. PBC could also improve separation of electron-hole (e--h+) pairs and enhance electron transfer ascribing to favorable carbon structure. Besides, PBC-Ago maintained good antimicrobial efficacy over E.coli DH5α. This work presented a facile carbothermal route to prepare Ago-based photocatalysts for dye removal and microbial inhibition in industrial wastewater.
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