An economical, fast, sensitive and selective method for the determination of uranium (VI) from sulfate media based on the flow injection on-line preconcentration in a minicolumn having amberlite IRA-402 (strong anion exchange) resin is described. Uranium (VI) was selectively adsorbed on the resin as uranyl trisulfate complex from aqueous solution of pH 2 in the minicolumn (2.56 mm i.d. and 7.5 cm in length) at a flow rate of 10 ml min(-1). The adsorbed uranyl trisulfate complex was eluted by HClO4 (0.1 mol l(-1), 6.5 ml min(-1)) and mixed with arsenazo-III (0.05 %, 6.5 ml min(-1)), and passed through the flow through cell of spectrophotometer where its absorbance was measured at 653 nm. Various parameters affecting adsorption and elution of the uranium complex were optimized. For data analyses peak absorbance was used. For 60 and 180 s preconcentration time, enrichment factors (EF) 20 and 40, sampling frequency (SF) 45 and 18 h(-1); and detection limits (DL) (3 sigma) 14.2 and 8.6 mu g l(-1) were obtained, respectively. To enhance the sensitivity of the system, two minicolumns (described above) were used for simultaneous preconcentration and elution purpose. For 60 and 180 s preconcentration time, EF 30 and 50, SF 42 and 17 h(-1) and DL (3 sigma) 4.4 and 3.44 mu g l(-1) were obtained, respectively. The effect of various anions and cations was studied for single column manifold. High selectivity of this method was observed. All the anions and cations studied did not interfere up to 330 times higher mass ratio to 300 mu g l(-1) U (VI) except Th(IV) which was tolerated up to 133 times by the addition of washing step in the manifold. The method based on single column manifold was applied on the spiked tap water, biological sample CRM (IAEA-V4) and synthetic leach liquor solution and good recovery was obtained. The method based on dual column manifold was validated on lake sediment SL-1 (CRM) and the results obtained were in good agreement at 95 % confidence level with the given value.