Analysis of Bromide Ion in Wine by Ion Selective Electrode

1976 ◽  
Vol 59 (1) ◽  
pp. 53-55
Author(s):  
James E Graf ◽  
Troy E Vaughn ◽  
William H Kipp

Abstract The use of the bromide ion selective electrode for the determination of bromide ion in wine has been found to be rapid and reliable. The method has been used for still wines and carbonated wines and is applicable to all wines regardless of their country of origin. The method consists of treating a 50 ml aliquot of wine with 2 ml each of 3.75M H3PO4, saturated KNO3, and 1M CuSO4. After 10 min the electrodes are immersed in the samples and a millivolt reading is obtained. One hundred μl 500 ppm bromide ion standard is added and the millivolt reading is taken. Bromide ion concentration in the wine = (CΔ × 1)/((antilog ΔE/S) − 1) where CΔ = 1, ΔE = the change in potential expressed in millivolts, and S = the electrode slope.

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.


2016 ◽  
Vol 21 (1) ◽  
pp. 76-81 ◽  
Author(s):  
Armila Rajbhandari Nyachhyon ◽  
Krishna Manandhar ◽  
Raja Ram Pradhananga

Bromide ion selective electrode (Br-ISE) have been successfully fabricated in the laboratory. The polycrystalline Ag2S-AgBr membrane material of Br-ISE was prepared by co-precipitation of silver sulphide and silver bromide from aqueous solution and was characterized by X-ray diffractometry (XRD). XRD results showed that material is in mixed phase state having Ag3SBr, Ag2S and AgBr. Scanning electron microscopy (SEM) has been used to study the texture of the surface. The potentiometric response has been investigated by 2 electrode system whereas 3 electrode systems have been used for electrochemical impedance spectroscopy (EIS). The electrode was found to behave well up to the bromide concentration of 1x10-5M with a Nernstian slope of 58 mV per decade change in bromide ion concentration. The selectivity coefficient of electrode containing bromide ion in the presence of I- and Cl- ions was found to be 3.98 and 8x10-2, respectively indicating that I- and Cl- ions interfere in the response of bromide electrode to bromide ion. The EIS studies shows that the charge transfer process is the key mechanism that is going on at the electrode/ electrolyte interface and electrode/ back contact interface.Journal of Institute of Science and TechnologyVol. 21, No. 1, 2016, page: 76-81


1986 ◽  
Vol 69 (1) ◽  
pp. 67-69
Author(s):  
Ezzat M Abdel-Moety ◽  
Abdel-Kader S Ahmad ◽  
Mohie Sharaf El-Din

Abstract A semimicro method for determination of iodine values of lipids is described. An accurately weighed smear of sample (10-20 mg) on a strip of ashless filter paper, 14 × 40 mm, is brominated with bromine vapors for about 5 min. Excess bromine adsorbed on the filter paper is allowed to sublime. Bromine absorbed by the sample is directly related to the degree of unsaturation. Paper with brominated sample is subjected to oxygen flask combustion in the presence of 2 mL 1M sodium hydroxide solution and 10 mL water as absorbing liquid. Bromide formed, which is equivalent to unsaturation, is determined by bromide ion selective electrode. Bromide ions can be also determined by gravimetry or by indirect argentometric titration. The results were statistically analyzed. The iodine values of some fatty acids and oils, determined by this technique, are in accord with those of some officially approved methods.


1984 ◽  
Vol 67 (4) ◽  
pp. 682-684
Author(s):  
John R Marzilli ◽  
◽  
F L Acampora ◽  
L R Alexander ◽  
M Y Alpert ◽  
...  

Abstract A proposed method using the fluoride (F) ion-selective electrode has been developed for determining the fluoride ion concentration in tablets and solutions containing sodium fluoride. The method has been subjected to collaborative study. Eight samples consisting of 2 authentic fluoride solutions, 2 commercial fluoride solutions, and 4 commercial fluoride tablets were sent to each of 11 collaborators together with a copy of the method. Single assays on the authentic fluoride solutions known to contain 1 mg F/5 mL were performed with average recoveries of 99.5 and 99.6% and relative coefficients of variation (CV) of 2.11 and 1.91%, respectively. Single assays of 2 commercial fluoride solutions declared at 1 mg F/5 mL gave mean values of 0.994 and 0.990 mg and relative CV values of 1.88 and 2.36%, respectively. Single assays of 2 commercial fluoride tablet preparations declared at 0.5 mg F gave mean values of 0.485 and 0.478 mg and relative CV values of 3.12 and 3.71 %, respectively. Single assays of 2 commercial fluoride tablet preparations declared at 1 mg F gave mean values of 0.991 and 0.981 mg and relative CV values of 2.99 and 2.85%, respectively. The method has been adopted official first action.


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.


Author(s):  
David C. Cowell

An automated method is described, using standard continuous flow techniques, for the determination of urine fluoride ion concentration using a fluoride ion selective electrode. It is shown that the kinetics of the electrode response to changes in fluoride ion can be used for the accurate measurement of fluoride ion concentration in urine, and that equilibration of the electrode response is not a prerequisite for the measurement of fluoride ion. Recovery experiments are in the range 83 to 90%; in-batch precision is between 0·9 and 1·6% and carryover 2·5% or less.


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