Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/95553
DC FieldValue
dc.titleComparison of Acid Mixtures in High-Pressure Microwave Digestion Methods for the Determination of the Total Mercury in Sediments by Cold-Vapor Atomic Absorption Spectrometry
dc.contributor.authorZhou, C.Y.
dc.contributor.authorWong, M.K.
dc.contributor.authorKoh, L.L.
dc.contributor.authorWee, Y.C.
dc.date.accessioned2014-10-16T08:49:13Z
dc.date.available2014-10-16T08:49:13Z
dc.date.issued1996
dc.identifier.citationZhou, C.Y.,Wong, M.K.,Koh, L.L.,Wee, Y.C. (1996). Comparison of Acid Mixtures in High-Pressure Microwave Digestion Methods for the Determination of the Total Mercury in Sediments by Cold-Vapor Atomic Absorption Spectrometry. Analytical Sciences 12 (3) : 471-476. ScholarBank@NUS Repository.
dc.identifier.issn09106340
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/95553
dc.description.abstractFour closed-vessel microwave digestion methods were compared for the accurate determination of mercury in sediments by flow-injection cold-vapor atomic absorption spectrometry. The results showed that several acid mixtures (HNO3/ H2SO4. HNO3/HClO4. HCl/HNO3 and HCl/ HNO3/HF) completely digested the soil matrix for the determination of mercury. The method using aqua regia is preferred because it is time saving, less dangerous and suitable for other trace7 metal analyses. The merits of pressure-feed back microwave digestion is that it simplifies soil sample digestion, and there is no loss of mercury. The digestion methods were evaluated by determining mercury in NIST SRM 1645 River Sediment. NIES CRM No. 2 Pond Sediment and NRCC BCSS-1 Marine Sediment. Recoveries of 92 108% were achieved. Good recoveries of 94 - 104% were also obtained for soil and marine-sediment samples spiked with different species of mercury.
dc.sourceScopus
dc.subjectCold-vapor atomic absorption spectrometry
dc.subjectMercury
dc.subjectMicrowave digestion
dc.subjectSediment
dc.subjectSoil
dc.typeReview
dc.contributor.departmentCHEMISTRY
dc.contributor.departmentBOTANY
dc.description.sourcetitleAnalytical Sciences
dc.description.volume12
dc.description.issue3
dc.description.page471-476
dc.description.codenANSCE
dc.identifier.isiutNOT_IN_WOS
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