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EurOCEAN 2000 - Vlaams Instituut voor de Zee

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LUMINESCENCE EQUIPMENT<br />

The equipment constructed by Edinburgh Instruments Ltd has been tested for steady and time<br />

<strong>de</strong>pen<strong>de</strong>nt fluorescence, for steady and time <strong>de</strong>pen<strong>de</strong>nt phosphorescence ; it remains to be<br />

tested for chemiluminesecence applications.<br />

PRECONCENTRATION<br />

The aim is to use immobilized quinolin-8ol for the preconcentration of seawater heavy metals.<br />

Various immobilization supports, usable in a fluidised bed reactor were consi<strong>de</strong>red. Among<br />

those, controlled pore glass (CPG) is found to be the most appropriate support material.<br />

CPG supported oxine has been synthesized. The material displays quantitative removal from<br />

the solution of most of the metals and shows suitable fluidisation behaviour.<br />

A fluidised bed reactor using the selected material has been <strong>de</strong>signed and tested. For all<br />

examined metals the yield of preconcentration is around 50% and does not vary significantly<br />

with flow rate<br />

A first improvement consists in the addition of a vibrator mixer. The effect of this modification<br />

is to increase the yield of trapping from ca. 50% to near 100%. The time required to obtain a<br />

given preconcentration ratio has been reduced. A one hundred folds preconcentration ratio in<br />

one hour is now possible. This results from the choice of a two-stage preconcentrator that<br />

inclu<strong>de</strong>s, in a first step, the removal of the solid and dissolved matrix by means of a fluidised<br />

bed. In a second step, the heavy metals are concentrated by means of a classical packed column.<br />

CADMIUM AND ZINC<br />

The monitoring of the two metals is based on the enhanced fluorescence intensities and<br />

modifications of the emission spectrum of aromatic-azamacrocycles systems induced by<br />

cations (A.W.Czarnik, 1992). As an example, the structure of an anthrylazamacrocycle is given<br />

in figure 1.<br />

Fig. 1<br />

Figure 1. Molecular structure of an anthrylazamacrocycle ; {1} is the molecule with five<br />

nitrogens<br />

In alkaline conditions, the fluorescence yield of {1} is very weak; when chelated to Zn or Cd<br />

large but <strong>de</strong>pending on the metal, dimension of the macrocycle and pH, chelation-enhanced<br />

fluorescence is observed.<br />

682<br />

NH<br />

NH NH<br />

N<br />

NH

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