In the fluoride separation of cerium, the use of thorium possessing similar ionic radius as coprecipitant in the presence of NH
4+ was introduced to the analysis of cast iron. The fluoride precipitate by this method is crystalline, so easy to handle in centrifugal tube, and moreover readily soluble in H
3BO
3 and H
2SO
4 mixture. The requisite time is shortened by eliminating the ignition of fluoride precipitate and successive dissolution by white-fuming with H
2SO
4 or HClO
4, and also the procedure is more simplified. The fundamental conditions of fluoride precipitation and photometric procedure are investigated. In the fluoride precipitation the optimum amounts of reagents are 15 mL of H
2SO
4(6 N), 10 mg of Th, 10 mL of HF, and 10 mL of NH
4OH in 100 mL of total volume. The amounts of H
3BO
3 and H
2SO
4 in the dissolution of fluoride precipitate give considerable effects on the absorbancy, and their optimum amounts at the color development are respectively 0.5 g and 5 mL in 80 mL of total volume. In the ultimate photometric determination, the absorbancy, is successfully measured at 320 mμ, and correction due to small amounts of adsorbed Fe
3+ etc. can be made by decolorizing the developed Ce
4+ alone with H
2O
2. The proposed method is suitable for determining 0.002∼0.1% of cerium in cast iron within about 1 hour.
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