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Determination of Manganese in Food Grade FeSO_4·7H_2O by Solid Phase Extraction and Flame Atomic Absorption Spectrometry

机译:固相萃取和火焰原子吸收光谱法测定食品级FeSO_4·7H_2O中的锰

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A new method for the determination of manganese in food grade FeSO_4·7H_2O samples by flame atomic absorption spectrometry (FAAS) after solid phase extraction was developed. The research showed that when coexistent amount of iron was greater than or equal to 100 times of manganese, the relative error of direct determination of manganese by FAAS was greater than or equal to +5%. Firstly, Fe~(2+) was oxidized to Fe~(3+) by HNO_3. Fe~(3+) was masked by EDTA. Mn~(2+) ions were then adsorbed by strong acid cation exchange fiber (SACEF) in pH 1.5 sample solution for 10 minutes and eluted by 2.5 mol/L HNO_3 for 15 minutes. Iron and manganese can be effectively separated by this method. Under the optimum conditions, the adsorption capacity of SACEF to Mn~(2+) ions was attained to be 9.27 mg·g~(-1). The detection limit of the method was 0.032 μg·mL~(-1). The proposed method was used for determination of manganese in three batches of FeSO_4·7H_2O samples. The contents of manganese were 325 μg/g, 823 μg/g, 772 μg/g respectively. The recoveries were in the range of 96.1%~103% and RSDs (n=5) were less than 3.0%.
机译:开发了固相萃取后火焰原子吸收光谱法测定食品级Feso_4·7H_2O样品中锰的新方法。该研究表明,当共存的铁数大于或等于100倍的锰时,FAA的直接测定的相对误差大于或等于+ 5%。首先,通过HNO_3将Fe〜(2+)氧化成Fe〜(3+)。 Fe〜(3+)被EDTA掩盖。然后将Mn〜(2+)离子在pH 1.5样品溶液中的强酸阳离子交换纤维(SACEF)吸附10分钟并在2.5mol / L HNO_3中洗脱15分钟。通过这种方法可以有效地分离铁和锰。在最佳条件下,SACEF至Mn〜(2+)离子的吸附能量达到9.27mg·g〜(-1)。该方法的检测限为0.032μg·mL〜(-1)。所提出的方法用于测定三批FeSO_4·7H_2O样品中的锰。锰的含量分别为325μg/ g,823μg/ g,772μg/ g。回收率在96.1%〜103%的范围内,RSDS(n = 5)小于3.0%。

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