This paper reports a new adsorptive voltammetric procedure of trace titanium determination using (Hg(Ag)FE) as a working electrode and chloranilic acid as a complexing agent. The reduction peak current of the complex was proportional to the concentration of Ti(IV) in the concentration range from 1×10 −8 molL −1 to 5×10 −7 molL −1 . Parameters that affect the titanium response, including solution pH, chloranilic acid concentration, accumulation potential and accumulation time, were optimized. Under optimum conditions the detection limit was 3.5×10 −9 molL −1 after 30s accumulation time. Under optimized conditions the quantitative Ti(IV) determination in the presence of as little as 30ppm of nonionic, 20ppm of anionic and 10ppm of cationic of surface active compounds, and 20ppm of natural organic matter can be performed. The proposed method was validated in the course of studying the recovery of Ti(IV) from spiked natural water samples.