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Polyion Selective Polymeric Membrane-Based Pulstrode as a Detector in Flow-Injection Analysis
Author(s) -
Andrea K. Bell-Vlasov,
Joanna Zajda,
Ayman Eldourghamy,
Elżbieta Malinowska,
Mark E. Meyerhoff
Publication year - 2014
Publication title -
analytical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.117
H-Index - 332
eISSN - 1520-6882
pISSN - 0003-2700
DOI - 10.1021/ac500567g
Subject(s) - chemistry , membrane , flow injection analysis , chromatography , analytical chemistry (journal) , pulse (music) , capillary electrophoresis , protamine , detector , ion exchange , thermal conductivity detector , potentiometric titration , electrode , detection limit , ion , heparin , gas chromatography , biochemistry , electrical engineering , organic chemistry , engineering
A method for the detection of polyions using fully reversible polyion selective polymeric membrane type pulstrodes as detectors in a flow-injection analysis (FIA) system is examined. The detection electrode consists of a plasticized polymeric membrane doped with 10 wt % of tridodecylmethylammonium-dinonylnaphthalene sulfonate (TDMA/DNNS) ion-exchanger salt. The pulse sequence used involves a short (1 s) galvanostatic pulse, an open-circuit pulse (0.5 s) during which the EMF of the cell is measured, and a longer (15 s) potentiostatic pulse to return the membrane to its original chemical composition. It is shown that total pulse sequence times can be optimized to yield reproducible real-time detection of injected samples of protamine and heparin at up to 20 samples/h. Further, it is shown that the same membrane detector can be employed for FIA detection of both polycations at levels ≥10 μg/mL and polyanions at levels of ≥40 μg/mL by changing the direction of the galvanostatic pulse. The methodology described may also be applicable in the detection of polyionic species at low levels in other flowing configurations, such as in liquid chromatography and capillary electrophoresis.

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