Solid-phase extraction of mono- and di-substituted organotin compounds in seawater

Citation
K. Ide et al., Solid-phase extraction of mono- and di-substituted organotin compounds in seawater, BUNSEKI KAG, 48(2), 1999, pp. 245-252
Citations number
13
Categorie Soggetti
Spectroscopy /Instrumentation/Analytical Sciences
Journal title
BUNSEKI KAGAKU
ISSN journal
05251931 → ACNP
Volume
48
Issue
2
Year of publication
1999
Pages
245 - 252
Database
ISI
SICI code
0525-1931(199902)48:2<245:SEOMAD>2.0.ZU;2-O
Abstract
The solid-phase extraction (SPE) of organotin compounds, such as monobutylt in (MBT), monophenyltin (MPT), dibutyltin (DBT) and diphenyltin (DPT) in se awater has been developed. An ion exchange-type solid-phase sorbent (Excelp ak SPE-ION/C224, Yokogawa Analytical Systems Inc., Japan) having a hydrophi llic and strong acidic sulfopropyl group and a cation-exchange resin (CK08P , Mitsubishi Chemicals,Japan) were comparatively investigated. The recovery of organotin compounds was measured by atomic-absorption spectrometry, and hydride purge & trap/ICP-MS in the case of ultratrace organotin compounds. The variables affecting SPE were investigated by using a 2.5% sodium chlor ide solution instead of seawater, such as the amounts of sorbent, the condi tioning of cation exchange resins, the flow rate and pH of sample solutions , the effect of the amounts of sodium ion, removing of adsorbed sodium, and an eluting agent. After all, thr cation exchange resin was chosen to be a SPE sorbent, because it has a higher ion-exchange capacity and exhibits bet ter recoveries of organotin compounds. Ten to twelve mi of a strong acidic cation exchange resin (pH 1.0) of sample solutions and a flow rate of 5 sim ilar to 6 mi min(-1) gave good results. For removing adsorbed sodium ions f rom the resins, 100 mi of 0.5 M hydrochloric acid was rinsed after injectin g every 125 mi of a sample solution of 2.5% sodium chloride solution contai ning organotin compounds. The eluent was 14 mi of 0.5 M hydrochloric acid-m ethanol solution. DBT and DPT were completely recovered from the solution u p to 500 mi of artificial seawater, also MBT and MPT were also recovered up to 250 mi. Ultra traces of MET, MPT, DBT and DPT were determined perfectly by using die present SPE system followed by the hydride purge & trap/ICP-M S.