A new MgCa–silica material with bimodal pore size is impregnated with KMnO₄ for dynamic adsorption of H₂S. The MgCa–silica was synthesized using sodium silicate and calcium and magnesium salts as precipitating agents. The KMnO₄ impregnation onto MgCa–silica was obtained through either direct addition into MgCa–silica wet coagulum or doping of dried MgCa–silica pellets into KMnO₄ solution. These chemisorbents were characterized by nitrogen physisorption, spectrophotometer, microscopy and dynamic H₂S adsorption test setup similar to ASHRAE standard I45.I. The results show that impregnation route and KMnO₄ wt% cause a reduction of surface area and total pore volume. The decrease in pore volume was slightly more in chemisorbents obtained via post doping compared to direct impregnation. Regardless of pore volume reduction the pore size range, 1–32 nm, was as in the parent MgCa–silica with micro and meso-pore diameter centered at 1.4 and 5.4 nm respectively. Thus obtained chemisorbents have their pore entrances neither blocked nor shifted. The MgCa–silica/KMnO₄ chemisorbents exhibits good H₂S uptake performance. The chemisorbent with 11.4 wt% KMnO₄ and obtained via direct impregnation possesses the highest uptake capacity. The lowest capacity was observed for chemisorbent with 8 wt% KMnO₄ and made by direct impregnation. The variations in uptake capacity are likely due to impregnation route, the KMnO₄ content and its location in the pore system. The results suggest that the MgCa–silica/KMnO₄chemisorbents can remove H₂S from indoor air at room temperature.