T h e dissolution of Cr-rich oxides in and the decontamination of contaminated specimens by sulfuric acid-Ce(N) (SC) solution have been investigated. T h e results have been compared with those by the reported typical decontamination reagents. T h e SC solution can dissolve simultaneously not only Cr but also F e and Ni in the Cr-rich oxides. T h e dissolution mainly depends on Ce(IV) concentration (1.3-10 x lo-, M) and temperature (40-90°C), but is independent of HzS04-concentration (0.2-0.5 M a t 5 x lo-, M Ce(IV)) . T h e DF is ca. 33 a t 90°C for 24 h with 0.25 M H2S04-5 x lo-, M Ce(N). Under electrolytic regeneration of Ce(lV) from Ce(III) during the decontamination, the D F is raised to 460 even a t 80°C for 24 h with 0.25 M H2S04-1.3x lo-, hi Ce(lV). T h e SC solution can be applicable to the decontamination for decommissioning of both BWR and PWR. Furthermore the combination of the chemical cleaning with an additional ultrasonic cleaning provides a promissing cleaning procedure for post-disassembly components.