Ammonium selective fluorosensor based on the principles of coextraction

The overall objective of this study was to develop an optical fluorosensor (optode) for real-time measurements of ammonium concentrations in natural l iquid samples. An NH4+ optode that can be used at such conditions should be analyte specific and independent of ionic strength and pH within a range n ormally found in such samples (pH 6-8; I-tot 0-700 mM). Additional desired sensor feature is a short response time (preferably minutes or less). This work presents an NH4+ fluorosensor that utilizes similar principles previou sly described for a K+ selective fluorosensor, i.e. coextraction of a nonac tin-ammonium complex and a solvatochromic dye in a hydrogel-ether emulsion. The sensor was tested for its selectivity for ammonium ions compared to ot her solutes from which interferences frequently have been reported, e.g. K and H+. Furthermore, sensor performance at different ionic strengths (I) w as evaluated. The ammonium fluorosensor was found to be (i) analyte specifi c with a selectivity coefficient (K-NH4+.K+(opt)) of 7 x 10(-2), i.e. senso r membranes are about twice as selective to ammonium relative potassium com pared to previous studies of electrochemical sensors; (ii) pH independent w ithin the interval 6.0-7.8; (iii) dependent on ionic strength within the in terval 100-700 mM, with optimal performance at lowest I-tot evaluated (100 mm); (iv) has a response time of less than 4 min; (v) has the ability to re versibly sense NH4+ even at muM levels. Sensor dynamic range was estimated as 10 muM-100 mM NH4+ in a sample matrix with ionic strength of 100 mM. Con struction, configuration and composition of sensor membranes make the ammon ium fluorosensor several times reusable, with a sensor shelf life time of a t least 8 months. (C) 2001 Elsevier Science B.V. All rights reserved.