Abstract

A method to determine low levels of iodine species namely I − and IO 3 − in aqueous samples was developed and applied to milk and milk powder samples. It is based on selective preconcentration of I − in polymer inclusion sorbent (PIS) and neutron activation analysis (NAA) of I − sorbed in PIS. The PIS was found to be highly selective for I − in presence of IO 3 − and other anions commonly present in the milk samples. In order to preconcentrate total I − + IO 3 − content in the PIS, IO 3 − was reduced to I − using a mixture of acetic acid and ascorbic acid. It was found that total iodine content in milk could be determined with epithermal neutron activation analysis (ENAA). A scheme was developed to determine I −, IO 3 − and total iodine. The developed method was applied to milk reference materials (NIST SRM-1549 and IAEA-RM-153 milk powder) and a commercially available milk powder. The scheme for estimation of iodine in different forms was validated by using reference material NIST SRM-1549.

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