Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/94237
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dc.titleMicrowave digestion of fish tissue for selenium determination by differential pulse polarography
dc.contributor.authorLan, W.G.
dc.contributor.authorWong, M.K.
dc.contributor.authorSin, Y.M.
dc.date.accessioned2014-10-16T08:33:44Z
dc.date.available2014-10-16T08:33:44Z
dc.date.issued1994-01
dc.identifier.citationLan, W.G.,Wong, M.K.,Sin, Y.M. (1994-01). Microwave digestion of fish tissue for selenium determination by differential pulse polarography. Talanta 41 (1) : 53-58. ScholarBank@NUS Repository.
dc.identifier.issn00399140
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/94237
dc.description.abstractIn KIO3NH3NH4Cl medium, the selenium complex Se(O)SO2- 3, resulted from the reaction of selenite and sulphite in acid solution, gave a catalytic wave, which was applied to the determination of selenium in fish by differential pulse polarography. The sample was decomposed using the HNO3/H2SO4/H2O2 digestion mixture in a closed PTFE digestion vessel with microwave heating. The detection limit was 0.06 μg/dm3. The calibration curve was linear up to 8 μg/dm3. Selenate present was reduced with hot hydrochloric acid to selenite. The recoveries of the selenite and selenate in two spiked samples investigated ranged from 91 to 104%. The NIES CRM No. 6 mussel was analyzed and the results obtained agreed well with the reference value (reference value: 1.5 μg/g; found: 1.43 ± 0.05 μg/g). The results obtained by differential pulse polarography were in good agreement with those found by hydride generation atomic absorption spectrometry. © 1993.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentZOOLOGY
dc.contributor.departmentCHEMISTRY
dc.description.sourcetitleTalanta
dc.description.volume41
dc.description.issue1
dc.description.page53-58
dc.description.codenTLNTA
dc.identifier.isiutNOT_IN_WOS
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