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PDF file - Facultatea de Chimie şi Inginerie Chimică

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252<br />

LIDIA VARVARI, SORIN-AUREL DORNEANU, IONEL CĂTĂLIN POPESCU<br />

PCI – 6024 E<br />

interface<br />

PC – AO – 2DC<br />

interface<br />

Figure 5. The scheme of the computer-controlled <strong>de</strong>vice<br />

used for the ISE potentiometric measurements;<br />

MS – magnetic stirrer; P – peristaltic pump<br />

IV. Experimental procedure<br />

Before use, all electro<strong>de</strong>s were conditioned for at least 24 hours in<br />

the solution containing the cation to be <strong>de</strong>termined.<br />

The experimental procedure consisted in two main parts: in the first<br />

one, the potentiometric response of the prepared membranes was recor<strong>de</strong>d<br />

for Ca 2+ , Mg 2+ , Na + , K + , NH4 + and Li + using separate solutions, and the<br />

corresponding calibration curves were recor<strong>de</strong>d. In the second part, the<br />

ionic interference between K + and different common cations was examined.<br />

All potentiometric measurements were performed in batch mo<strong>de</strong>, using the<br />

standard addition method for the preparation of standard solutions.<br />

For the interference study, the method of fixed primary ion concentration<br />

was used: the primary ion concentration was kept constant, while the<br />

concentrations of the interfering ions were increased.<br />

ACKNOWLEDGMENTS<br />

Electro<strong>de</strong> 1<br />

Electro<strong>de</strong> 2<br />

Electro<strong>de</strong> 3<br />

Electro<strong>de</strong> 4<br />

Ref. electro<strong>de</strong><br />

Electrochemical<br />

interface<br />

Controll<br />

unit<br />

Electrochemical<br />

cell<br />

The authors are grateful to dr. Elisabeth-Jeanne Popovici from the<br />

“Raluca Ripan” Chemistry Research Institute for providing the compound<br />

C6Es6 and to ANCS for the financial support.<br />

MS<br />

P

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