شماره ركورد كنفرانس :
4014
عنوان مقاله :
Preparation of electrochemical sensor base on carbon paste electrode modified by a new pentazene ligand for determination of mercury in aqueous samples
پديدآورندگان :
Payehghadr Mahmood Payame Noor University , Hashemi Seyed Majid Payame Noor University , Nourifard Farzaneh Payame Noor University , Ali Karimi Mohammad Payame Noor University
كليدواژه :
Carbon paste electrode , pentazadiene , Mercury , Electrochemical sensor. Figure 1. Chemical structure of 1 , 5 , bis(4 , methoxyphenyl) , 3 , methyl , 1 , 4 , pentazadiene (b , PMMP)
عنوان كنفرانس :
دوازدهمين سمينار سالانه الكتروشيمي ايران
چكيده فارسي :
As one of the most toxic heavy metals, mercury pollution has attracted much attention in
environmental and toxicological domains for decades. Inorganic mercury released mainly from
industrial sources can be further converted into methylmercury by microorganisms and fish.
Methylmercury, the most common organic mercury, is more toxic than inorganic mercury because
it’s lipophilic and easily absorbed by aquatic organisms which finally bioaccumulate in the human
body through the food chain leading to severe impact on human health due to its severe toxicity to
the nervous and immune system[1].
Nowadays,different schemes have been reported for detection of water-soluble Hg2+ ion, e.g.,
colorimetricassay, electrochemical method, inductively coupled plasma mass spectroscopy (ICPMS)
and fluorescencespectroscopy. Among the methods, electrochemistry holds great potential as
the next-generation detection strategy because of its high sensitivity, low cost, low power
requirements and simple instrumentation[2]
In this study, a new ligand, 1,5-bis(4-methoxyphenyl)-3-methyl-1,4-pentazadiene (b-PMMP)
(figure 1) has been synthesized by reaction of the 4-methoxyaniline (p-anisidine) with
methanamine (methylamine). The mixture was stirred in an ice bath for 30 min. The structure of the
synthesized compound resulted from the IR and 1H NMR and 13C NMR. Afterwards, a carbon
paste electrode modified with a this new ligand was developed for the mercury determination at
nanomolar level concentration. The electrochemical behavior of this molecule was investigated
employing cyclic voltammetry and square wave voltammetric. The experiments were conducted
with a certain electrode composition of 18.0% paraffin oil, 70.0% high purity graphite powder and
12.0% b-PMMP as well as the usage of pH=10 ammonia buffer as supporting electrolyte. Also the
enhanced peak current response is a clear evidence of the modified carbon paste electrode towards
oxidation of mercury. The effect of pH and scan rate on the electrode process was investigated. The
resulting electrode demonstrated linear response across a wide mercury concentration range. The
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method was successfully applied to the determination of water-soluble Hg2+ ion in environmental
samples.