SciELO - Scientific Electronic Library Online

 
vol.55 número3SYNTHESIS AND EVALUATION OF HEPATOPROTECTIVE ACTIVITY OF SOME NEW MANNICH BASES BEARING BENZTRIAZOLE MOIETYELECTROCHEMICAL STUDIES AND EXTRACTION OF CHEMICAL AND ELECTROCHEMICAL PARAMETERS OF ZN(II) ION AT MERCURY ELECTRODE VIA CONVOLUTIVE VOLTAMMETRY AND DIGITAL SIMULATION METHODS índice de autoresíndice de assuntospesquisa de artigos
Home Pagelista alfabética de periódicos  

Serviços Personalizados

Journal

Artigo

Indicadores

Links relacionados

Compartilhar


Journal of the Chilean Chemical Society

versão On-line ISSN 0717-9707

J. Chil. Chem. Soc. v.55 n.3 Concepción  2010

http://dx.doi.org/10.4067/S0717-97072010000300022 

J. Chil. Chem. Soc, 55, N° 3 (2010) 371-373

 

COPPERII-SELECTIVE ELECTRODES BASED ON 1-FUROYL-3,3-DIETHYLTHIOUREA AS A NEUTRAL CARRIER

M. DE LOS A. ARADA PÉREZ1*, SANTIAGO LANDAZURY YANES1, M. CARDONA1, L. AGUILERA1 M.YAZDANI-PEDRAM2

1Department of Analytical Chemistry, Eastern University of Cuba, Santiago de Cuba. e-mail: may@cnt.vo.edu.cu

2Polymer Laboratory, Faculty of Chemical and Pharmaceutical Sciences, University of Chile, Sergio Livingstone Pohlhammer 1007, Independencia, Santiago, Chile.


ABSTRACT

1-furoyl-3,3-diethylthiourea was used as a novel neutral carrier in ion selective electrode for copperII detection and determination. The Cu2+ selective plasticized polyvinyl chloride (PVC) membrane electrode exhibited reversible potential responses with Nernstian slope of 29.34± 0.6 mV/decade for Cu2+ ions in the concentration range from 1.0x10-7 to 1.0x10-2 mol/dm3 with a practical detection limit (PDL) of 3.84x10-7 and lower limit of linear response (LLLR) of 6.15x10-7 mol/dm3 and alife-time of 20 days. The response time, pH effect and other characteristics of the electrodes were also studied.

Keywords: Neutral carrier; CopperII-selective potentiometric sensor; Ion-selective electrode (ISE).


 

INTRODUCTION

Copper can be found in many kinds of food, in drinking water and in air. The absorption of copper is necessary, because copper is a trace element that is essential for human health. Although humans can handle proportionally large concentrations of copper, too much copper can still cause eminent health problems. However, copper deficiency causes anemia1. Environmental effects of copper occur when it ends up in soil. Copper strongly attaches to organic matter and minerals. As a result, it does not travel very far after release and it hardly ever enters groundwater. In surface water copper can travel great distances, either suspended on sludge particles or as free ions. Therefore, the presence of copper in the environment can affect the human and animal health and a fast efficient method of its determination is necessary.

Potentiometric measurements with copper ion selective electrode allow the direct determination of free Cu2+ ion concentration in aqueous samples. Ion-selective electrodes (ISEs) based on ionophores are widely used 2-12 and plasticized polyvinyl chloride (PVC) membrane ISEs based on several kinds of neutral carriers, such as Schiff s bases2-11, calixazacrown ether3 as typical ionophore are convenient for determining ionic species in analytical chemistry and environmental monitoring.

The present study describes polymer membrane electrodes responsive to Cu2+ ions based on 1-furoyl-3,3-diethylthiourea as a new neutral carrier containing chelating sites.

EXPERIMENTAL

Materials and methods

The water used in this work was bidistilled water with a conductivity of less than 2 mS/cm-1. All the reagents used in this study were of analytical grade. Poly(vinylchloride) (PVC) from Fluka was used as polymeric matrix. The plasticizer used was dioctyl phthalate (DOP) from Riedel-de Haen and was employed as solvent mediator of the PVC liquid membrane. Tetrahydrofurane (THF) was analytical grade from Merck The 1-furoil-3,3-dietiltiourea was synthesized in the laboratory of natural products of the University of Havana, Cuba. The epoxy conducting resin was prepared by mixing Araldite M and Hardener H form Ciba-Geigy and graphite powder from Merck as already described by Arada Pérez et.al.13-14 for nitrate sensors obtaining a resistance of≤2 kΩ.

A pH/mv meter OAKLON digital pH meter with a precision of ± 0.1 mV was used for measuring the potential difference between reference and indicator electrodes. The reference electrode used in this study was an Ag/ AgC1 HI 5311 double junction electrode and a solution of 0.1 mol/dm3 of K2SO4 was employed in the external electrode compartment. Amicroprocessor Hanna pH meter model 213 was used for measuring the pH with a combined electrode with epoxy body Oaklon model WD-35881-00 and a hot plate-stirrer Jenway model 1000 LT.

Preparation of the membranes

The preparation of the electrode body and the application of the membrane were carried out in a similar manner as the method used for the construction of the all-solid-state ion selective electrodes reported in the literature13-14. The prepared membranes contained 6 Wt. % of 1-furoyl-3,3-diethylthiourea as ionophore, 61 Wt. % of dioctyl phthalate as plasticizer and 33 Wt. % of PVC as the polymeric matrix.

Determination of the electromotive force (EMF)

The electromotive force (EMF) determinations were carried out by using a cell at 25 ± 0.5°C The composition of the electrochemical cell was:

Ag/AgCl|KCl                      0.1mol/dm3|K2SO4             0.1mol/dm3||test

solution||PVCmemb.|cond. supp. |Cu(s)

The calibration curves were used to calculate such parameters as slope (S), practical detection limit (PDL) and Lower Limit of Linear Response (LLLR). This was done following the Nernst law through data adjustment by linear regression method. The calibration parameters were obtained by applying the method of additions15, determining the activity of the principal ion by using the Debye-Hückel equation (equation 1).

 

The selectivity coefficients (KPot) were determined by using the method of mixed solutions15 through the equation 2.

 

Figure 1: Structure of l-furoil-3,3-diethylthiourea employed as ionofore.

RESULTS AND DISCUSSION

The calibration parameters obtained from calibration curves of electrodes are shown in table 1. It is seen from this table that the constructed electrodes responded adequately to Cu2+ ions, the values for the slope (S) correspond to those expected by Nernst for a divalent anion. Figure 2 shows the calibration curve obtained for Cu2+ ions, evidenced the good linearity of the calibration curves for the plasticizer used as solvent mediator in this study. The calibration curve was checked repeatedly during 20 days, in the time of life of the electrode, for five replies of the electrode (n=5).

 

Figure 2: Calibration curve obtained by the method of additions for Cu2 ISE with 1-furoil-3,3-diethylthiourea as neutral carrier.

Response time

The response time of the electrode was evaluated by immersing the electrode in a solution of primary ion (10-2 mol/dm3) and reading the electrode potential to acquiere a stable value.

These response characteristics were repeatedly found throughout the lifetime of the electrode. The data presented in figure 3 were obtained with an electrode which was used under normal working conditions for 20 days.

 

Figure 3: Potential stability as function of time for Cu2+ ISE for a concentration of primary ions of 10-2 mol/dm3.

Influence of pH on the response of the electrodes

The effect of pH on the response of the electrodes was studied in this work by using the corresponding Reilley's diagram. An adjustment of pH was performed using dilute sodium hydroxide and nitric acid. The studied pH intervals for the constructed electrodes are shown in figure 4. The experimental results showed that the variation of pH affected notably the electrode potential. It is seen from figure 4 that the electrode potential remains constant in pH intervals of 8.Oto 10.0.

 

Figure 4: pH Dependence of the response of Cu2+ ion selective electrode for a concentration of primary ions of 10-2 mol/dm3.

Study of the effect of interfering cations on the selectivity of the constructed ISE

The quantification of the selectivity of the constructed electrodes can be obtained by measuring the degree of the interference of different ions on the response of the electrode for cupper ion. This was done by determining the corresponding potentiometric selectivity coefficient15 (KPot) in the presence of different interfering ions and the results are shown in table 2 together with the results obtained by sadeghi et. al. who used different Schiff base derivatives, 2,2-[4,4-diphenyl-methanebis(nitrilomethylidyne)]-bisphenol (L1) and 2,2-[4,4-diphenylsulfonebis (nitrilomethylidyne)]-bis(4-methyl phenol) (L6) as ionophors10.

 

As can be seen from table 2, the Zn2+ presented major interference by the constructed ISE, where the interfering order was Zn2+ > Na+ > K+.

The results obtained in this study were compared with those obtained by Sadeghi et. al. who used different Schiff base derivatives as ionofore10. The degree of interference observed for the electrodes constructed in this work was different compared to those electrodes constructed by using Schiff base derivatives L1 and L6, where much more interference was observed in the case of 1-furoil-3,3-diethylthiourea.

CONCLUSIONS

A new PVC membrane ion selective electrode for copper (II) was constructed by using 1-furoil-3,3-diethylthiourea as a neutral carrier (ionophore). The prepared Cu2+ ISEs showed almost the same Nernstian slope for Cu2+ with a practical detection limit (PDL) of 3.84x10-7 mol/dm3 and a response time of 20 s. The Cu2+ ISE worked effectively in the pH range of 8.0-10.0 and had a lifetime of 20 days.

REFERENCES

1.- H. Scheinberg, A. G. Morell, Inorganic Biochemistry, Elsevier, Amsterdam 1973.         [ Links ]

2.- A. R. Fakhari, T. A. Raji, H. H. Naeimi, Sens. Actuators B: Chem., 104, 317(2005)         [ Links ]

3.- S. J. Park, O. J. Shon, J. A. Rim, J. K. Lee, J. S. Kim, H. Nam, H. Kim, Talanta, 55(2), 297(2001)         [ Links ]

4.- M. H. Mashhadizadeh, A. Mostafavi, R. Razavi, M. Shamsipur, Sens. Actuators B: Chemical, 86(2-3), 222 (2002)         [ Links ]

5.- S. Yoshimoto, H. Mukai, T. Kitano, Y. Sohrin, Anal. Chim. Acta, 494, 207(2003)         [ Links ]

6.- M. Shamsipur, A. Avanes, M. Javanbakht, M. R. Ganjali, H. Sharghi, Anal. Sci., 18, 875 (2002)        [ Links ]

7.- M. Shamsipur, M. Javanbakht, M. F. Mousavi, M. R. Ganjali, V. Lippolis, A. Garau, L. Tei, Talanta, 55, 1047 (2001)         [ Links ]

8.- E. Bakker, P. Buhlmann, E. Pretsch, Talanta, 63, 3 (2004)         [ Links ]

9.- E. Bakker, P. Buhlmann, E. Pretsch, Electroanalysis, 11(13), 915 (1999)         [ Links ]

10.- S. Sadeghi, M. Eslahi, M. A. Naseri, H. Naeimi, H. Sharghi, A. Shameli. Electroanalysis, 15(15-16), 7527(2003)         [ Links ]

11.- M.B. Gholivand, M. Rahimi-Nasrabadi, M.R. Ganjali, M. Salavati-Niasari, Talanta, 73, 553 (2007)         [ Links ]

12.- Shin-ichi Wakida, Nagahisa Sato, Keiitsu Saito, Sens. and Actuators B: Chemical, 130 787 (2008)         [ Links ]

13.- M. A. Arada, L. Pérez-Marín, J. Calvo, M. Yazdani-Pedram, Sens. Actuators B: Chemical, 89, 262 (2003)         [ Links ]

14.- M. de los Á. Arada Pérez, M. Yazdani-Pedram. J. Chil. Chem. Soc. 49 (3), 227(2004)         [ Links ]

15.- IUPAC "Compendium of Analytical Nomenclature Oxford Pergamon Press", 168-173 (1978)        [ Links ]

(Received: January 20, 2010 - Accepted: July 14, 2010)

 

Creative Commons License Todo o conteúdo deste periódico, exceto onde está identificado, está licenciado sob uma Licença Creative Commons