Kinetic studies with ion-selective electrodes: determination of creatinine in urine with a picrate ion selective electrode: a laboratory experiment

1983 ◽  
Vol 60 (1) ◽  
pp. 74 ◽  
Author(s):  
E. P. Diamandis ◽  
M. A. Koupparis ◽  
T. P. Hadjiioannou
1970 ◽  
Vol 7 (7) ◽  
pp. 19-23 ◽  
Author(s):  
A Rajbhandari ◽  
AP Yadav ◽  
K Manandhar ◽  
RR Pradhananga

The polycrystalline materials obtained by co-precipitation of silver sulphide and appropriate silver halide are used to prepare silver sulphide based membrane electrodes selective to the silver, chloride, bromide, iodide, and sulphide ions. The powder materials are characterized by x-ray diffraction, SEM equipped with EDAX. These membrane electrodes are found to give Nernstian response with the appropriate ions in the concentration range from 1x10-1 to 1x10-5 M. The performance of these home made electrodes is at par with the commercial electrodes. The electrodes have been successfully used for the quantitative determination of chloride, bromide iodide, silver, and sulphide ions and also for the determination of thiamine in pharmaceutical preparations. For developing countries like Nepal, who can not afford to procure high cost commercial ion selective electrodes, these home made ion selective electrodes are especially appealing since the electrode can be fabricated with ease in low cost and the electrode is well behaved and sufficiently accurate for the analysis with ion selective electrodes. Key words: Ion selective electrode; Home made ion selective electrode; Silver sulphide; Thiamine; Vitamin B1. DOI: 10.3126/sw.v7i7.3818 Scientific World Vol.7(7) 2009 pp.19-23  


2010 ◽  
Vol 117 ◽  
pp. 7-14
Author(s):  
Raja Ram Pradhananga ◽  
A. Nyachhyon ◽  
A.P. Yadav ◽  
Lok Kumar Shrestha ◽  
S. Tandukar

An electrochemical sensor based on the silver sulphide precipitate was fabricated in the laboratory and characterized by x-ray diffraction, SEM equipped with EDAX, and electrochemical techniques. Ion selective electrode (ISE) was found to be sensitive enough to sense the sulphide ion concentration from 10-1 to 10-5 M in alkaline medium. The change in electrode potential per decade change in sulphide ion concentration was found to be 31.5 mV at laboratory temperature indicating adherence of the ion selective electrode to Nernst’s equation. The sensor have been successfully used for the quantitative determination of thiamine in pharmaceutical preparations, hydrogen sulphide in cigarette smoke and determination of solubility products of sparingly soluble silver salts. A trace amount of hydrogen sulphide, a toxic gas, is present in the cigarette smoke. The quantitative estimation of hydrogen sulphide in cigarette smoke is a challenging task to analytical chemist. Hydrogen sulphide in cigarette smoke had been determined by absorbing the cigarette smoke in 0.1 M sodium hydroxide and the resulting solution was analyzed using silver sulphide based ion sensor by standard addition technique using modified Gran plot. The average amounts of hydrogen sulphide produced by a stick of cigarette in 8 different brands of Nepalese cigarette ware found to range from 0.0332 mg to 0.0766 mg. The sensitivity and reliability of these home made ion sensors were excellent and in par with commercial electrodes. For developing countries like Nepal, who can not afford to procure high cost commercial ion selective electrodes, these home made ion sensors are especially appealing since the sensor can be fabricated with ease from the materials that are readily available in the chemistry laboratory and the sensor is quite sensitive and gives reproducible results which are sufficiently accurate for the analysis with ion selective electrodes.


1981 ◽  
Vol 27 (8) ◽  
pp. 1435-1438 ◽  
Author(s):  
G B Levy

Abstract The advent of ion-selective electrodes made possible the potentiometry of sodium in serum and plasma. These methods were based on dilution of serum, as done in flame photometry, and the results were identical. Analysis of whole blood precludes dilution and so "direct" potentiometry was developed. Results by this technique are variable but tend to compensate for the spurious hyponatremias found by the "indirect" dilution methods due to displacement of volume by lipids and protein. However, there is no unambiguous theoretical basis on which to choose between the various direct ion-selective-electrode techniques and instruments. As an alternative, I propose use of current indirect methods, with numerical correction for the shift in normal sodium values in the presence of abnormal lipid and (or) protein. A table was constructed for making such corrections.


1981 ◽  
Vol 46 (2) ◽  
pp. 368-376 ◽  
Author(s):  
Josef Veselý

Titration of sulphates with lead perchlorate employing lead ion selective electrode indication was studied using additions of various organic solvents at different pH' and ionic strength values. As the optimum emerged systems with 60-70% 1,4-dioxane, pH' 5.3-5.6. After dehydration with sodium hydroxide, dioxane must be freed from the electrode surface-oxidizing impurities by their reduction with sodium metal and subsequent distillation. The method was applied to determination of sulphates in mountain spring waters. Units of ppm can be determined; the limit of determination, however, depends considerably on the content of dioxane, total salt content in the sample, and speed of the semi-automatic titration. Lead can be determined with EDTA in concentrations down to c(Pb2+) = 5 . 10-6 mol l-1.


Chemosensors ◽  
2021 ◽  
Vol 9 (7) ◽  
pp. 155
Author(s):  
Yan Su ◽  
Ting Liu ◽  
Caiqiao Song ◽  
Aiqiao Fan ◽  
Nan Zhu ◽  
...  

As an essential electrolyte for the human body, the potassium ion (K+) plays many physiological roles in living cells, so the rapid and accurate determination of serum K+ is of great significance. In this work, we developed a solid-contact ion-selective electrode (SC-ISE) using MoS2/Fe3O4 composites as the ion-to-electron transducer to determine serum K+. The potential response measurement of MoS2/Fe3O4/K+-ISE shows a Nernst response by a slope of 55.2 ± 0.1 mV/decade and a low detection limit of 6.3 × 10−6 M. The proposed electrode exhibits outstanding resistance to the interference of O2, CO2, light, and water layer formation. Remarkably, it also presents a high performance in potential reproducibility and long-term stability.


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