Abstract

Tetrabenzyl pyrophosphate and diphenylphosphinic anhydride, with two phosphoryl groups (PO) as ligating sites, can be used as novel ionophores to make Pb 2+-selective membrane electrodes. A good result was obtained with tetrabenzyl pyrophosphate, and the electrode based on this ionophore and bis(1-butylpentyl) adipate as a solvent mediator in a poly(vinyl chloride) membrane matrix exhibited a near-Nernstian response to Pb 2+ in the concentration range of 1×10 −5–1×10 −2 M with a slope of 28.7 mV per concentration decade in a solution containing 0.1 M Mg(NO 3) 2. The limit of detection was 3×10 −6 M. The selectivity of this electrode to other metal cations was comparable to the best case in many Pb 2+-selective electrodes so far developed. Addition of potassium tetrakis( p-chlorophenyl)borate (40 mol% relative to tetrabenzyl pyrophosphate) caused a drastic change in the response slope (53.3 mV per concentration decade), probably due to the formation of PbA +, where A stands for anions present in the sample solution, and decreased significantly the electrode selectivity to other metal cations.

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