Inspired by the development of an adsorbent material with a high capacity for chlorinated gas treatment, an -Fe 2 O 3 nanoparticle deposited activated carbon adsorbent was successfully synthesized. The -Fe 2 O 3 NPs synthesis was done by a facile chemical precipitation method using sodium hydroxide (NaOH) as a precipitant agent. The variation of the molar ratio of the reactant and precipitant (i.e. 1:1, 1:1.5, 1:2 by mole) and of the precipitating temperature (i.e. 50, 70, 90C) were explored. The physical and chemical characteristics of the synthesized samples were examined using various techniques; Transmission Electron Microscope (TEM), Brunauer-Emmett-Teller analysis (BET), Thermogravimetry analysis (TGA), Fourier Transform Infra-Red (FT-IR) and Ultraviolet-Visible spectrophotometer. The result shows that two synthesized conditions-1:1 by mole (FeCl 3 :NaOH) at 70C and 1:1.5 by mole (FeCl 3 :NaOH) at 90C-were allowed to produce the smallest size of -Fe 2 O 3 NPs approximately 10 nm. Consequently, it gave the highest specific surface area of 110 m 2 /g. With a higher FeCl 3 : NaOH molar ratio and a higher precipitating temperature, the synthesized Fe 2 O 3 NPs formed a more oval shape with a finer surface. Due to the insufficient purification, unfortunately, an impurity caused by sodium salt was detected in the amount of 5-10 wt.%. The minimum amount of 75 wt.% -Fe 2 O 3 NPs coated on the activated carbon was observed. The production yield of the synthesized -Fe 2 O 3 and -Fe 2 O 3 /GAC samples was also reported.