scholarly journals Flow injection programmed to function in batch mode is used to determine molar absorptivity and to investigate the phosphomolybdenum blue method

Talanta ◽  
2019 ◽  
Vol 201 ◽  
pp. 519-526 ◽  
Author(s):  
Jaromir (Jarda) Ruzicka ◽  
Graham D. Marshall ◽  
Christopher I. Measures ◽  
Mariko Hatta
2019 ◽  
Vol 30 (3) ◽  
pp. 28
Author(s):  
Nisreen Kais Abood ◽  
Mohammed Jasim M. Hassan ◽  
Muneer A. AL-Da'amy

Three simple, sensitive, selective, accurate and efficient spectrophotometric methodsfor determining cefixime in bulk drug and pharmaceutical formulations havedescribed. The first method involved conversion of NH 2 in cefixime to diazoniumsalt, which has coupled with Bisphenol A in an alkaline medium. The orange coloredproduct showed λ max at 490 nm and followed Beer's law over a concentration range of1-50 μg mL -1 , with molar absorptivity of 0.866×10 4 L.mol -1 .cm -1 and the detectionlimit was 0.157 μg.mL -1 . The second method involved pre-concentration of a traceamount of cefixime-azo dyes using cloud point extraction (CPE). The extracted drug-dye was spectrophotometrically measured at λ max 500. The constructed calibrationcurve to determine cefixime followed Beer’s law in a range of 0.25-6 μg.mL -1 , with acorrelation coefficient of 0.9998, molar absorptivity of 0.961×10 5 L.mol -1 .cm -1 andthe detection limit was equal to 0.031 μg.mL -1 . The pre-concentration factor was 25and distribution coefficient (D) was 314.03.A diazotization of the studied drug (cefixime) and its coupling with Bisphenol A wasstudied using a developed flow injection analysis method, based on the detection ofthe absorption of the diazotization product. Chemical and physical properties [ofwhat??] were studied to develop the suggested method and to determine the stabilityof the colored of product. A flow rate of 2.5 mL.min -1 , 50 cm reaction coil and 100μL sample volume were used to operate the system and the orange colored productwas detected at 490 nm. The proposed three methods were successfully applied todetermine cefixime in pharmaceutical formulation, where results were satisfactory


2010 ◽  
Vol 14 (02) ◽  
pp. 158-165 ◽  
Author(s):  
Saeed S. Beheshti ◽  
Fatemeh Sohbat ◽  
Mohammad K. Amini

Metalloporphyrin-based ion-selective electrodes for flow-injection potentiometric determination of thiocyanate are described. The detection system is based on a coated glassy carbon electrode membrane sensor incorporating 5,10,15,20-tetraphenyl-21H,23H-porphine manganese(III) chloride as the active ingredient. The influences of the membrane composition, pH, and the effects of flow-injection parameters on the response of the system were investigated. At the optimized flow-injection potentiometric conditions, the sensor exhibited a Nernstian slope of -58.0 mV per decade of thiocyanate activity over the range 4.2 × 10-7–7.6 × 10-2M , where 50 μL of each sample solution was injected into the carrier solution. The detection limit of thiocyanate in the FIP mode was 4.2 × 10-7M . The selectivity of the flow-injection potentiometric system with respect to several common inorganic and organic anions was superior to that of the batch mode using the same sensor and similar operating conditions. The sensor was applied to the determination of thiocyanate in urine samples.


1997 ◽  
Vol 19 (2) ◽  
pp. 45-50 ◽  
Author(s):  
A. N. Tripathi ◽  
S. ehikhalikar ◽  
K. S. Patel

This paper explains a new procedure for flow injection analysis (FIA) determination of iron in rain water based on the colour reaction of Fe3+with thiocyanate ions in the presence of the cationic surfactant cetylpyridinium chloride (CPC). The value of apparent molar absorptivity of the complex in terms of iron is (2.00) x 104l mole-1cm-1at an absorption maximum of 490 nm. The detection limit of the method is 8 ppb Fe. The sample throughput is 90 samples/h at a flow rate of 4.0 ml/min. The reaction mechanism, optimization of FIA variables, and effect of various types of surfactant are described. None of the tested anions and cations interfered with the determination of iron. The method was used for the quantification and flux determination of iron in rain water.


2019 ◽  
Vol 9 (02) ◽  
Author(s):  
Nisreen Kais Abood ◽  
Mohammed Jasim M Hassan ◽  
Muneer A AL-Da,amy

TThree methods study in this research simple, sensitive, an expensive and rapid Oxidative Coupling reaction, Cloud Point Extraction and Flow Injection spectrophotometric methods for determination Methyldopa and Salbutamol, the first method oxidative coupling reaction between the Methyldopa and thiosemicarbazide in presence of ferric nitrate anhydrous to yield dark green colored product that have absorbance at λ max 460 nm. Salbutamol coupling reaction with 4-nitrophenyl hydrazine in presence the potassium Iodide and sodium hydroxide to product the violet colored has absorbance at λ max 530 nm. Beer’s law is obeyed from (1-50) µg/ mL with sandall’s sensitivity (0.039,0.073), correlation coefficient (0.9998) and molar absorptivity (0.536×104,0.327×104) for Methyldopa and Salbutamol respectively. The secondly method to estimation the trace amount of phenolic drugs that product from the oxidative coupling reaction it is cloud point extraction, cloud point extraction enables the drugs to be precisely estimated under the optimal experimental conditions, the maximum absorption at λ max (470,535) nm respectively. The concentration was range (0.25-6) µg/mL, molar absorptivity 0.510×105 ,0.483×105 and enrichment factor (9.51,14.72) respectively for Methyldopa and Salbutamol.Flow injection analysis is simple method to determination the phenolic is based on the measurement of absorption signal for product resulting from oxidative coupling reaction , study all experimental parameters chemical and physical to development and stability the colored of product .Total flow injection of 1.5mL/min was pumped and active material was detect at λ max (460,530)nm respectively for Methyldopa and Salbutamol . In this the proposed methods were suxciffuly, applied to the determination Methyldopa and Salbutamol in pharmaceutical preparation.


2020 ◽  
Vol 36 (6) ◽  
pp. 1066-1077
Author(s):  
Irene Nalumansi ◽  
Grace Birungi ◽  
Brenda Moodley ◽  
Emmanuel Tebandeke

A simple spectrophotometric method for the determination of low levels of the orthophosphate (PO43-) in environmental water systems is reported. The method is based the formation of the phosphomolybdate from the condensation of molybdate and orthophosphate in aqueous acid medium followed by reduction with sodium thiosulphate to form phosphomolybdenum blue. The system obeys Beer’s law at 880 nm (λmax) in the 0.005–0.06 mg P mL-1 phosphate concentration range. Molar absorptivity, Sandell’s sensitivity and correlation coefficient values for the determination were 57526 L mol-1 cm-1, 0.2835 μg cm-2 and 0.9948 respectively. The limit of detection was 2.213 x 10-3 mg P mL-1. The results of PO43- determination in water samples obtained using the spectrophotometric method developed in this study, compare favourably with those generated using the Murphy and Riley method which is commonly used for this analysis. Therefore, the study ably demonstrates the suitability of the present spectrophotometric method for analysis of the orthophosphate in environmental water samples.


2018 ◽  
Author(s):  
Vishnu Prakash K ◽  
Siddesh Desai ◽  
Hrishikesh Gadgil ◽  
Vinayak Kulkarni

2013 ◽  
Vol 12 (7) ◽  
pp. 460-465
Author(s):  
Sameer Amereih ◽  
Zaher Barghouthi ◽  
Lamees Majjiad

A sensitive colorimetric determination of fluoride in drinking water has been developed using a polymeric zirconium complex of 5-(2-Carboxyphenylazo)-8-Hydroxyquinoline as fluoride reagents. The method allowed a reliable determination of fluoride in range of (0.0-1.5) mg L-1. The molar absorptivity of the complex formation is 7695 ± 27 L mol-1 cm-1 at 460 nm. The sensitivity, detection limit, quantitation limit, and percentage recovery for 1.0 mg L-1 fluoride for the proposed method were found to be 0.353 ± 0.013 μg mL-1, 0.1 mg L-1, 0.3 mg L-1, and 101.7 ± 4.1, respectively.


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