It is vital to recycle precious metals effectively such as silver from waste sources because of limited natural reserves. Herein, passion fruit (Passiflora edulis Sims) shell-derived S-doped porous carbons (SPCs) were newly synthesized by hydrothermal carbonization and following with activation by KOH/(NH4)2SO4, and the adsorption of Ag+ on SPC under acidic solutions was investigated. It was found that the activator of (NH4)2SO4 can not only introduce the doping of S elements but also increase the proportion of mesopores in the as-prepared SPC. As the active site, the increasing S doping can improve the adsorption of Ag+ on SPC. The kinetic data of Ag+ adsorption by SPC was consistent with the pseudo-second-order kinetic model. The Langmuir isothermal model was used to well fit the Ag+ adsorption isotherms of SPC, and the maximum adsorption capacity of the optimized SPC-3 for Ag+ is up to 115 mg/g in 0.5 mol/L HNO3 solution. SPC-3 showed good selectivity toward Ag+ over diverse competing cations, which is mainly attributed to the strong bonding between Ag+ ions and the sulfur-containing functional groups on the surface of SPC-3 resulting in the formation of Ag2S nanoparticles. The adsorbed Ag could be recovered as an elemental form by a simple calcination. This study provides a new insight into the design of an environmentally friendly and efficient adsorbent for the selective recovery of silver from acidic aqueous media.
Keywords: Ag+ adsorption; S doping; biomass-derived carbon; recovery; selectivity.