scholarly journals Potentiometric Determination of Chlorate Impurities in Hypochlorite Solutions

2019 ◽  
Vol 2019 ◽  
pp. 1-7 ◽  
Author(s):  
Dmitry V. Girenko ◽  
Al’ona A. Gyrenko ◽  
Nikolai V. Nikolenko
Keyword(s):  
Sodium Hypochlorite ◽  
Sodium Sulfite ◽  
Systematic Errors ◽  
Expanded Uncertainty ◽  
Iodide Ions ◽  
Low Concentrations ◽  
Sophisticated Equipment ◽  
The Matrix ◽  
Fold Excess

The method of iodometric determination of chlorates impurities in sodium hypochlorite solutions for medical and veterinary purposes was developed. This method does not require sophisticated equipment and can be implemented directly where the solutions are used. The method is based on the different rates of interaction of ClO- and ClO3- with iodide ions depending on the acidity of the medium. We have shown that blank titration is advisable to improve the accuracy of the determination of low concentrations of chlorates in the matrix of hypochlorite which is present in excess since in this case possible systematic errors due to the presence of oxidizing impurities in the reagents are prevented. To quantify the low concentrations of chlorates, we proposed to remove 85-95% of hypochlorite ions by means of reducing their excess with sodium sulfite at pH 10.5. The solution of sodium sulfite does not require standardization before each analysis in the proposed procedure. The possibility of quantitative determination of chlorate impurities in the range of 2-50 mg/L in the presence of 50-500–fold excess of sodium hypochlorite with an error of 5% has been proved. The expanded uncertainty of chlorate determination did not exceed 0.6 mg/L.

THE COLORIMETRIC DETERMINATION OF PLATINUM WITH 5-(p-DIMETHYLAMINOBENZYLIDENE)-RHODANINE

1963 ◽  
Vol 41 (3) ◽  
pp. 667-670 ◽  
Author(s):  
Frances E. Piercy ◽  
D. E. Ryan
Keyword(s):  
Ascorbic Acid ◽  
The Other ◽  
Colorimetric Determination ◽  
Platinum Metals ◽  
Low Concentrations ◽  
Fold Excess

5-(p-Dimethylaminobenzylidene)-rhodanine is used to determine 0.5 to 6 p.p.m. of platinum colorimetrically, after reduction of platinum IV with ascorbic acid. Platinum can be determined in the presence of a 10-fold excess of palladium; low concentrations of the other platinum metals, except rhodium, do not seriously interfere.

Voltammetric and Potentiometric Determination of Gold in Gold-Plated Electrotechnical Components

1993 ◽  
Vol 58 (9) ◽  
pp. 2039-2046 ◽  
Author(s):  
Karel Vytřas ◽  
Ivan Švancara ◽  
František Renger ◽  
Malis Srey ◽  
Radmila Vaňková ◽  
...  
Keyword(s):  
Differential Pulse ◽  
Indicator Electrode ◽  
Carbon Paste ◽  
The Matrix ◽  
Plastic Membrane ◽  
Pulse Voltammetry ◽  
Paste Electrode ◽  
Fold Excess ◽  
Selective Accumulation

Differential pulse voltammetry was used to determine gold in gold-plated electrotechnical components. Samples were dissolved to form tetrachlorourate, which was determined on a carbon paste electrode containing tricresyl phosphate as pasting liquid. A characteristic cathodic peak for tetrachlorourate, whose selective accumulation is based on extraction, is obtained during cathodic scan from +0.8 to -0.5 V vs Ag/AgCl electrode. The accompanying Fe(III) and Cu(II) ions from the matrix are masked by adding EDTA. Gold can be determined in the presence of their thousand-fold excess in the concentration range 1 . 10-5 - 1 . 10-7 mol l-1. The results were confirmed by potentiometric titration with a solution of 1-(ethoxycarbonyl)pentadecyltrimethylammonium bromide (Septonex) by using a coated-wire indicator electrode with a softened plastic membrane.

scholarly journals Analytical Strategies for the Determination of Arsenic in Rice

2016 ◽  
Vol 2016 ◽  
pp. 1-11 ◽  
Author(s):  
Bruno E. S. Costa ◽  
Luciana M. Coelho ◽  
Cleide S. T. Araújo ◽  
Helen C. Rezende ◽  
Nívia M. M. Coelho
Keyword(s):  
Inorganic Arsenic ◽  
Sample Pretreatment ◽  
Fertilizer Application ◽  
Low Concentrations ◽  
The Matrix ◽  
Analytical Strategies ◽  
Recent Developments ◽  
Route Of Exposure ◽  
High Concentrations

Arsenic is an element of concern given its toxicological significance, even at low concentrations. Food is a potential route of exposure to inorganic arsenic and in this regard arsenic in rice is associated with soil contamination, fertilizer application, and the use of arsenic-containing irrigation water. Therefore, there is a need to investigate the regional rice crops with a view to future discussions on the need for possible regulatory measures. Several studies have reported high concentrations of arsenic in rice grown in soils irrigated with contaminated water; however, procedures used, including sample pretreatment and preconcentration steps, have to be followed to ensure sensitivity, accuracy, and reproducibility. Arsenic is a difficult element to measure in complex matrices, such as foods, because the matrix must be destroyed at an elevated temperature without the loss of the analyte or contamination. This review summarizes the major methods for the determination of arsenic in rice samples. The main purpose of this review is to provide an update on the recent literature concerning the strategies for the determination of arsenic and to critically discuss their advantages and weaknesses. These difficulties are described along with recent developments aimed at overcoming these potential issues.

Statistics and parallaxes

1978 ◽  
Vol 48 ◽  
pp. 7-29
Author(s):  
T. E. Lutz
Keyword(s):  
Experimental Design ◽  
Statistical Methods ◽  
Review Paper ◽  
Systematic Errors ◽  
Past Experience ◽  
Random Errors ◽  
Trigonometric Parallaxes ◽  
Systematic And Random Errors

This review paper deals with the use of statistical methods to evaluate systematic and random errors associated with trigonometric parallaxes. First, systematic errors which arise when using trigonometric parallaxes to calibrate luminosity systems are discussed. Next, determination of the external errors of parallax measurement are reviewed. Observatory corrections are discussed. Schilt’s point, that as the causes of these systematic differences between observatories are not known the computed corrections can not be applied appropriately, is emphasized. However, modern parallax work is sufficiently accurate that it is necessary to determine observatory corrections if full use is to be made of the potential precision of the data. To this end, it is suggested that a prior experimental design is required. Past experience has shown that accidental overlap of observing programs will not suffice to determine observatory corrections which are meaningful.

Lateral resolution of the electron microbeam analysis

1978 ◽  
Vol 36 (1) ◽  
pp. 542-543
Author(s):  
H.J. Dudek
Keyword(s):  
Quantitative Analysis ◽  
Depth Resolution ◽  
Lateral Resolution ◽  
Cylindrical Particle ◽  
Correction Procedure ◽  
X Ray ◽  
Element Concentrations ◽  
Microbeam Analysis ◽  
The Matrix

The chemical inhomogenities in modern materials such as fibers, phases and inclusions, often have diameters in the region of one micrometer. Using electron microbeam analysis for the determination of the element concentrations one has to know the smallest possible diameter of such regions for a given accuracy of the quantitative analysis.In th is paper the correction procedure for the quantitative electron microbeam analysis is extended to a spacial problem to determine the smallest possible measurements of a cylindrical particle P of high D (depth resolution) and diameter L (lateral resolution) embeded in a matrix M and which has to be analysed quantitative with the accuracy q. The mathematical accounts lead to the following form of the characteristic x-ray intens ity of the element i of a particle P embeded in the matrix M in relation to the intensity of a standard S

Determination of the phase structure of polymerblends by electron microscopy

1978 ◽  
Vol 36 (1) ◽  
pp. 492-493
Author(s):  
Dr. G. Kaemof
Keyword(s):  
Screw Extruder ◽  
Electron Microscopic ◽  
Thin Sections ◽  
Single Screw Extruder ◽  
Transmission Electron ◽  
The Matrix ◽  
Twin Screw ◽  
Special Case ◽  
Microscopic Investigations

A mixture of polycarbonate (PC) and styrene-acrylonitrile-copolymer (SAN) represents a very good example for the efficiency of electron microscopic investigations concerning the determination of optimum production procedures for high grade product properties.The following parameters have been varied:components of charge (PC : SAN 50 : 50, 60 : 40, 70 : 30), kind of compounding machine (single screw extruder, twin screw extruder, discontinuous kneader), mass-temperature (lowest and highest possible temperature).The transmission electron microscopic investigations (TEM) were carried out on ultra thin sections, the PC-phase of which was selectively etched by triethylamine.The phase transition (matrix to disperse phase) does not occur - as might be expected - at a PC to SAN ratio of 50 : 50, but at a ratio of 65 : 35. Our results show that the matrix is preferably formed by the components with the lower melting viscosity (in this special case SAN), even at concentrations of less than 50 %.

Polishing process effect on the image of dispersed precipitates

1984 ◽  
Vol 42 ◽  
pp. 534-535
Author(s):  
C.T. Hu ◽  
C.W. Allen
Keyword(s):  
Matrix Material ◽  
Specimen Preparation ◽  
Second Phase ◽  
Precipitate Particle ◽  
Polishing Process ◽  
Second Phase Particles ◽  
The Matrix ◽  
Surface Profiles ◽  
Thinning Process

One important problem in determination of precipitate particle size is the effect of preferential thinning during TEM specimen preparation. Figure 1a schematically represents the original polydispersed Ni3Al precipitates in the Ni rich matrix. The three possible type surface profiles of TEM specimens, which result after electrolytic thinning process are illustrated in Figure 1b. c. & d. These various surface profiles could be produced by using different polishing electrolytes and conditions (i.e. temperature and electric current). The matrix-preferential-etching process causes the matrix material to be attacked much more rapidly than the second phase particles. Figure 1b indicated the result. The nonpreferential and precipitate-preferential-etching results are shown in Figures 1c and 1d respectively.

Development of a method for multielemental determination in water by EDXRF with radioisotopic source of 238Pu.

2019 ◽  
Vol 7 (2A) ◽  
Author(s):  
Camilo Fuentes Serrano ◽  
Juan Reinaldo Estevez Alvares ◽  
Alfredo Montero Alvarez ◽  
Ivan Pupo Gonzales ◽  
Zahily Herrero Fernandez ◽  
...  
Keyword(s):  
Thin Layer ◽  
Expanded Uncertainty ◽  
Considerable Decrease ◽  
X Ray ◽  
Precipitation Efficiency ◽  
Method Of Determination ◽  
Sensitivity Curves ◽  
Order Of Magnitude ◽  
Metrological Parameters

A method for determination of Cr, Fe, Co, Ni, Cu, Zn, Hg and Pb in waters by Energy Dispersive X Ray Fluorescence (EDXRF) was implemented, using a radioisotopic source of 238Pu. For previous concentration was employed a procedure including a coprecipitation step with ammonium pyrrolidinedithiocarbamate (APDC) as quelant agent, the separation of the phases by filtration, the measurement of filter by EDXRF and quantification by a thin layer absolute method. Sensitivity curves for K and L lines were obtained respectively. The sensitivity for most elements was greater by an order of magnitude in the case of measurement with a source of 238Pu instead of 109Cd, which means a considerable decrease in measurement times. The influence of the concentration in the precipitation efficiency was evaluated for each element. In all cases the recoveries are close to 100%, for this reason it can be affirmed that the method of determination of the studied elements is quantitative. Metrological parameters of the method such as trueness, precision, detection limit and uncertainty were calculated. A procedure to calculate the uncertainty of the method was elaborated; the most significant source of uncertainty for the thin layer EDXRF method is associated with the determination of instrumental sensitivities. The error associated with the determination, expressed as expanded uncertainty (in %), varied from 15.4% for low element concentrations (2.5-5 μg/L) to 5.4% for the higher concentration range (20-25 μg/L).

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