Abstract

Speciation analysis calls for rapid, simple systems for minimizing errors made in the most troublesome of all steps in the analytical process: sample preparation. In this context, continuous-flow systems are of great help. The evolution in the different methodologies enabled solutions to the main shortcomings occurring from the lack of selectivity of using RP–C18 as sorbent material. One solution was a shift to more sensitive and selective, but only partially automated, systems employing C60 fullerene and Grignard’s reagent; another was a shift to completely automated systems employing sodium tetrapropylborate; and a final solution was to employ the simplest possible configuration by removing the reagent stream. The analytical methods developed allowed the identification and quantification of different organolead species at the pg/ml levels in rainwater samples, with precision (RSD) of about 5% and recoveries ranging from 92 to 100%.

Highlights

  • Organolead compounds are released into the atmosphere by direct evaporation from gasoline during transport and storage or as a consequence of the incomplete combustion of the leaded gasoline in explosion motors

  • Volatile tetraalkyllead compounds or particle-adsorbed ionic alkyllead compounds can be transported long distances until they are dissolved by the rain and sent back to the ground, where they reach superficial and groundwaters

  • NaBPr4 has been used in a continuous-flow system in order to enable the complete automation of the speciation procedure for organolead compounds[5]

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Summary

Short Communication

Innovations in the Speciation of Organolead Compounds in Water: Towards a More Rational, Rapid, and Simple Analytical Process. Speciation analysis calls for rapid, simple systems for minimizing errors made in the most troublesome of all steps in the analytical process: sample preparation. In this context, continuous-flow systems are of great help. The evolution in the different methodologies enabled solutions to the main shortcomings occurring from the lack of selectivity of using RP–C18 as sorbent material. The analytical methods developed allowed the identification and quantification of different organolead species at the pg/ml levels in rainwater samples, with precision (RSD) of about 5% and recoveries ranging from 92 to 100%.

INTRODUCTION
CHEMICALS AND INSTRUMENTATION
SPECIATION OF ORGANOLEAD COMPOUNDS
CONCLUSIONS
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