eCite Digital Repository
A novel ion chromatographic method based on cation-exchange and acid-base interactions for the simultaneous determination of total alkalinity and monovalent cations in samples of mu l volume
Citation
Hu, W and Haddad, PR and Hasebe, K and Tanaka, K, A novel ion chromatographic method based on cation-exchange and acid-base interactions for the simultaneous determination of total alkalinity and monovalent cations in samples of mu l volume , Analyst, 126, (5) pp. 555-558. ISSN 0003-2654 (2001) [Refereed Article]
![]() | PDF Restricted - Request a copy 395Kb |
Copyright Statement
Copyright © 2001 Royal Society of Chemistry
Official URL: http://www.rsc.org
DOI: doi:10.1039/b101820p
Abstract
An ion chromatographic (IC) method based on the use of
titrant (strong acid) as the stationary phase was developed
for simultaneous determination of total alkalinity (TA) and
monovalent cations. The titrant used in this study was
obtained by initially loading lithium dodecylsulfate (Li-DS)
onto a reversed-phase material and then conditioning the
column with a slightly acidified aqueous LiCl solution (a
mixture of 50.0 mM LiCl and 0.1 mM H2SO4). When a small
amount of a basic sample was injected onto a column
prepared in this way, the basic species (Bn2) reacted
predominantly with H+ on the stationary phase and the
reaction with the eluent phase was negligible due to the very
low concentration of eluent H+ (in the eluent, a molar ratio
of [Li+]/[H+] = 250 + 1 applied). The stationary phase H+
consumed in the acid–base reaction was then re-supplied by
H+ from the eluent. By monitoring the conductance of the
eluent using conductivity, an induced peak resulting from
the basic species was observed. Calibration graphs of peak
areas vs. molar concentration of the basic species for OH2,
HCO32 and H2PO42 were found to be identical. CO3
22,
HPO4
22, and B4O7
22 also gave identical calibration curves
but their slope values were twice those for HCO32. The
detection limit for HCO32 was less than 3.2 μM and the
calibration curve was linear up to 12.3 mM (injection
volume, 100 μL). Seawater was directly analyzed and its
total alkalinity was found to be 2.87 mM (RSD 0.53%, n =
5), which was in good agreement with the result of 2.88 mM
(RSD 3.2%, n = 5) obtained using auto-potentiometric
titration. Na+ and K+ were determined simultaneously and
the concentrations were 481.6 and 10.6 mM, respectively.
Item Details
Item Type: | Refereed Article |
---|---|
Research Division: | Chemical Sciences |
Research Group: | Analytical chemistry |
Research Field: | Separation science |
Objective Division: | Expanding Knowledge |
Objective Group: | Expanding knowledge |
Objective Field: | Expanding knowledge in the chemical sciences |
UTAS Author: | Haddad, PR (Professor Paul Haddad) |
UTAS Author: | Tanaka, K (Dr Kazuhiko Tanaka) |
ID Code: | 22141 |
Year Published: | 2001 |
Web of Science® Times Cited: | 6 |
Deposited By: | Chemistry |
Deposited On: | 2001-08-01 |
Last Modified: | 2011-08-03 |
Downloads: | 0 |
Repository Staff Only: item control page