Pw. Alexander et al., PHOTO-CURED AMMONIUM AND HYDROGEN-ION SELECTIVE COATED-WIRE ELECTRODES USED SIMULTANEOUSLY IN A PORTABLE BATTERY-POWERED FLOW-INJECTION ANALYZER, Electroanalysis, 9(17), 1997, pp. 1331-1336
Nonactin and N,N-dioctadecylmethylamine ionophores, each in an epoxydi
acrylate polymer, were photo-cured on silver wires (0.8 mm i.d.) and e
valuated as ammonium and hydrogen (pH) coated wire electrodes. The pho
to-cured membranes prepared in this study exhibited excellent adhesion
to the metal substrate and improved mechanical strength compared to P
VC based membranes. The ammonium electrode exhibited a Nernstian respo
nse over a concentration range between 0.01 mM and 100 mM with a detec
tion limit of 0.0005 mM. The ammonium electrode exhibited improved sel
ectivity against most common interfering ions, including potassium com
pared to previous studies. The hydrogen selective electrode exhibited
a near-Nernstian slope of 55.9 +/- 0.8 mV change/log a((H+)) between p
H 4.0 and pH 11.0 in the steady-state mode. The ammonium and pH sensor
s each responded quickly reaching 90% of steady-state value in<5s, mak
ing these coated wire sensors ideal for flow injection potentiometry m
easurements. In the FIP mode, both the photo-cured ammonium and pH ele
ctrodes exhibited near-Nernstian responses of 49.2 +/- 1.0 mV change/a
ctivity decade and 50.2 +/- 0.4 mV change/log a((H+)), respectively, o
ver a similar concentration range as in the steady-state mode. The pho
to-cured ammonium and pH electrodes were used simultaneously in the an
alysis of hydroponic nutrient solutions and waste water samples obtain
ed from a local greenhouse grower in the dow injection potentiometric
mode.