scholarly journals Extractive Spectrophotometric Determination of Pd(II) with Sodium Salt of Hexamethyleneiminecarbodithioate

2013 ◽  
Vol 23 ◽  
pp. 20-28
Author(s):  
S.D. Dhanavate ◽  
D.J. Garole ◽  
V.J. Garole ◽  
S.R. Tetgure ◽  
A.D. Sawant
Keyword(s):  
Metal Ions ◽  
Spectrophotometric Determination ◽  
Sodium Salt ◽  
Accurate Determination ◽  
Chelating Agent ◽  
Molar Absorptivity ◽  
Real Samples ◽  
Highly Sensitive ◽  
Ph Range

The reagent NaHMICdt·2H2O has found to be a good chelating agent for the spectrophotometric determination of various metal ions. The present investigation deals with spectrophotometric determination of Pd(II) by using NaHMICdt·2H2O. The reagent reacted with Pd(II) to give yellow complex extractable into toluene. Pd (II) was extracted quantitatively in the pH range 0.5-2.0. Pd(II)-HMICdt complex showed λmax at 435 nm. The extracted species has a 1:2 (M:L) stoicheometry. Beer’s law is obeyed in the range of 0.2-0.8 μg ml-1 of Pd (II). The molar absorptivity and the sandells sensitivity were found to be 0.754 x 104 lmol-1cm-1 and 0.0140 μg mol-1 cm-2 respectively. The effect of divers ion on the extraction of Pd(II) has been investigated. The proposed method is highly sensitive, selective, and simple and rapid has been applied for accurate determination of palladium in synthesis mixtures and real samples.

scholarly journals Micelle-mediated extraction of cobalt and its spectrophotometric determination in rocks, soils, sediments and sea-bed polymetallic nodules

2019 ◽  
Author(s):  
Chem Int ◽  
Pranab Kumar Tarafder
Keyword(s):  
Spectrophotometric Determination ◽  
Certified Reference Materials ◽  
Molar Absorptivity ◽  
Present System ◽  
Sea Bed ◽  
Soil Sediment ◽  
Polymetallic Nodules ◽  
Ph Range ◽  
Almost All

The surfactant sensitized bottle-green complex (1:2:1) formed of cobalt-thiocyanate-cetyltrimethylammonium bromide is suitably extracted into an organic solvent, ethylacetate, at a pH range, 6-8 and the absorption measurements were carried out at 630 nm (ƛmax). The Beer’s law is obeyed in the range from 0.05 to 10 μg per mL. The molar absorptivity and Sandell’s sensitivity of the present system were found to be 2.2 x 103 L.mol-1cm-1 and 0.026 μg cm-2, respectively. No other element forms complex of similar colour with thiocyanate at this pH range. The method was applied to a number of samples like rock, soil, sediment, polymetallic nodules etc., as well as Certified Reference Materials and the values were found highly satisfactory. The interference of Fe3+ which formed a reddish complex at acidic pH (<7) was eliminated when the complex was extracted at pH 8.0. The method is highly useful for the determination of cobalt in geological samples having its concentration from μg/mL to percentage level. As the method has been made highly selective for spectrophotometric determination of cobalt, it might be applied to almost all types of geological sample of diverse matrices.

scholarly journals Micelle-mediated extraction of cobalt and its spectrophotometric determination in rocks, soils, sediments and sea-bed polymetallic nodules

2019 ◽  
Author(s):  
Chem Int
Keyword(s):  
Spectrophotometric Determination ◽  
Certified Reference Materials ◽  
Molar Absorptivity ◽  
Present System ◽  
Sea Bed ◽  
Soil Sediment ◽  
Polymetallic Nodules ◽  
Ph Range ◽  
Almost All

The surfactant sensitized bottle-green complex (1:2:1) formed of cobalt-thiocyanate-cetyltrimethylammonium bromide is suitably extracted into an organic solvent, ethylacetate, at a pH range, 6-8 and the absorption measurements were carried out at 630 nm (ƛmax). The Beer’s law is obeyed in the range from 0.05 to 10 μg per mL. The molar absorptivity and Sandell’s sensitivity of the present system were found to be 2.2 x 103 L.mol-1cm-1 and 0.026 μg cm-2, respectively. No other element forms complex of similar colour with thiocyanate at this pH range. The method was applied to a number of samples like rock, soil, sediment, polymetallic nodules etc., as well as Certified Reference Materials and the values were found highly satisfactory. The interference of Fe3+ which formed a reddish complex at acidic pH (<7) was eliminated when the complex was extracted at pH 8.0. The method is highly useful for the determination of cobalt in geological samples having its concentration from μg/mL to percentage level. As the method has been made highly selective for spectrophotometric determination of cobalt, it might be applied to almost all types of geological sample of diverse matrices.

Spectrophotometric determination of zinc with 5-methyl-1,3,4-thiadiazolyl-(2-azo-1)-2-naphthol

1983 ◽  
Vol 48 (2) ◽  
pp. 464-470 ◽  
Author(s):  
Juan Cacho ◽  
Cristina Nerin
Keyword(s):  
Spectrophotometric Determination ◽  
Organic Phase ◽  
Molar Absorptivity ◽  
Beer's Law ◽  
Optimum Ph ◽  
Beer’S Law ◽  
Ph Range ◽  
Optimum Ph Range

The reaction of Zn(II) with 5-methyl-1,3,4-thiadiazolyl-(2-azo-1)-2-naphthol (MTDAN) and extraction of the complex formed in chloroform is studied. The optimum pH range for the extraction and formation of the complex is 10-11.2 and Beer's law is obeyed in the interval of 0-2 ppm of Zn(II) in the organic phase. The molar absorptivity is 5.9 . 104 l mol-1 cm-1 at 568 nm. The stoichiometry of the complex corresponds to the type ML2. Some interferences are studied and an easy way is given to eliminate them. The results are compared with those corresponding to TAN. The reaction is applied to the analysis of synthetic samples of bronzes with satisfactory results.

scholarly journals A new reagent system for the highly sensitive spectrophotometric determination of selenium

2006 ◽  
Vol 4 (4) ◽  
Author(s):  
Hosakere Revanasiddappa ◽  
Banadahalli Dayananda
Keyword(s):  
Malachite Green ◽  
Spectrophotometric Determination ◽  
Reference Method ◽  
Cost Effective ◽  
Molar Absorptivity ◽  
Malachite Green Dye ◽  
Highly Sensitive ◽  
Optimum Reaction ◽  
Leuco Malachite Green

AbstractHighly sensitive and simple spectrophotometric determination of selenium is described for the determination of selenium(IV) using a new reagent leuco malachite green. The method is based on the reaction of selenium(IV) with potassium iodide in an acidic condition to liberate iodine, the liberated iodine oxidizes leuco malachite green to malachite green dye. The green coloration was developed in an acetate buffer (pH 4.2–4.9) on heating in a water bath (∼ 40 °C). The formed dye exhibits an absorption maximum at 615 nm. The method obeys Beer’s law over a concentration range of 0.04–0.4 µg mL−1 selenium. The molar absorptivity and Sandell’s sensitivity of the color system were found to be 1.67 × 105 L mol−1 cm-1 and 0.5 ng cm−2, respectively. The optimum reaction conditions and other analytical parameters have been evaluated. The proposed procedure has been successfully applied to the determination of selenium in real samples of water, soil, plant material, human hair, and cosmetic samples. The results were compared to those obtained with the reference method. Statistical analysis of the results confirms the precision and accuracy of the proposed method. In addition, the developed method is cost-effective and involves easily accessible instrumentation technique which can be used by ordinary research laboratories.

scholarly journals Difference spectrophotometric method for the determination of Fluphenazine hydrochloride in tablets using peroxomonosulfate

2021 ◽  
Vol 9 (2) ◽  
pp. 64-71
Author(s):  
Mykola Blazheyevskiy ◽  
◽  
Valeriy Moroz ◽  
Olena Mozgova ◽  
◽  
...  
Keyword(s):  
Quantitative Determination ◽  
Spectrophotometric Determination ◽  
Spectrophotometric Method ◽  
Present Method ◽  
Molar Absorptivity ◽  
Limit Of Quantification ◽  
Derivatizing Agent ◽  
Sensitive Method

The oxidative derivatization method using potassium hydrogenperoxomonosulfate for the indirect spectrophotometric determination of Fluphenazine hydrochloride is presented. Potassium hydrogenperoxomonosulfate is introduced as a derivatizing agent for Fluphenazine hydrochloride, yielding the sulfoxide. This reaction product was successfully used for the spectrophotometric determination of the Fluphenazine hydrochloride. The UV spectroscopic detection of the sulfoxide proved to be a more robust and sensitive method. The elaborated method allowed the determination of Fluphenazine hydrochloride in the concentration range of 0.2-30 µg mL-1. The molar absorptivity at 349 nm is 5.6×103 (dm3cm-1mol-1). The limit of quantification, LOQ (10S) is 0.24 µg/mL. A new spectrophotometric technique was developed and the possibility of quantitative determination of Fluphenazine hydrochloride in tablets 5.0 mg was demonstrated. The present method is precise, accurate and excipients did not interfere. RSD for Fluphenazine Hydrochloride 5.0 mg tablets was 1.37 %.

scholarly journals A Double-Line Sequential Injection System for the Spectrophotometric Determination of Copper, Iron, Manganese, and Zinc in Waters

2005 ◽  
Vol 88 (2) ◽  
pp. 639-644 ◽  
Author(s):  
Inês P A Morais ◽  
M Renata S Souto ◽  
António O S S Rangel
Keyword(s):  
Metal Ions ◽  
Spectrophotometric Determination ◽  
Absorption Spectrometry ◽  
Injection System ◽  
Sequential Injection ◽  
Double Line ◽  
Relative Standard ◽  
Iron Manganese ◽  
Determination Of Copper

Abstract A double-line sequential injection system was developed for the spectrophotometric determination of several metal ions in waters. The proposed double-line configuration was used to enable adding sample and chromogenic reagents as merging zones. The methodology was applied to the spectrophotometric determination of copper, iron, manganese, and zinc in samples of diverse origins at the range of 0.15–5.00, 0.10–10.0, 0.48–4.00, and 0.11–5.00 mg/L, respectively. Different chromogenic reagents and detection wavelengths were used. The chromogenic reagents for iron and manganese were 1,10-phenanthroline and formaldoxime, respectively. Copper and zinc were both determined using the analytical reagent zincon. Analytical characteristics of the methodology, such as manifold parameters, buffer pH, and reagent concentrations were optimized, and interference of some of the metal ions commonly present in water sample was assessed. Results of the analysis were in agreement with those obtained by atomic absorption spectrometry. Repeatability, expressed as the relative standard deviation for 10 consecutive injections of water samples, was lower than 6%. The determination rate was approximately 36/h.

K, Ca, Mg, and Zn in platelets, as determined by atomic absorption spectrometry with use of a sealed decomposition bomb and discrete nebulization.

1985 ◽  
Vol 31 (4) ◽  
pp. 609-612 ◽  
Author(s):  
T Makino
Keyword(s):  
Metal Ions ◽  
Atomic Absorption Spectrometry ◽  
Atomic Absorption ◽  
Accurate Determination ◽  
Absorption Spectrometry ◽  
New Method ◽  
Differential Centrifugation ◽  
Individual Variations

Abstract In this new method for precise and accurate determination of K, Ca, Mg, and Zn in platelets, small amounts of platelets, prepared by differential centrifugation and cell washing, are decomposed in a homemade mini-vessel, a sealed Teflon bomb. The metal ions in the decomposed sample are measured by atomic absorption spectrometry with discrete nebulization. Overall, CVs ranged from 0.8 to 4.8%. We investigated sex-related differences (none were found) and intra-individual variations.

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