RP-HPLC study of redox equilibria in vanadium-PAR binary and ternary systems: Direct determination of vanadium in steel

1997 ◽  
Vol 126 (3-4) ◽  
pp. 241-249 ◽  
Author(s):  
Sławomir Oszwałdowski ◽  
Maciej Jarosz
1972 ◽  
Vol 26 (1) ◽  
pp. 96-99 ◽  
Author(s):  
Mary Jo Calhoun ◽  
Edward S. DellaMonica

A method for the determination of individual components of complex mixtures is presented. The technique used is based on ir-absorbance measurements for stearic acid at 1700 and at 935 cm−1 when the concentration range exceeds 0.50% wt/vol; for isopropenyl stearate at 1145 and at 865 cm−1; for stearic anhydride at 1030 cm−1 and mixed stearic-acetic anhydride at 1000 cm−1. The baseline method was used in all absorbance measurements. Absorbance-concentration relationships obeyed Beer's law from 0 to 2.0% wt/vol for most compounds; the exception being stearic acid (at 1700 cm−1), where linearity was limited to a maximum 0.50% wt/vol. Due to spectral interference between the two anhydrides at low concentration ratios, an empirical percent transmission ratio method was used to estimate the relative concentration of each. Binary and ternary systems were studied and the standard deviations of the differences between theoretical and calculated values indicate that this method is reliable.


1980 ◽  
Vol 45 (4) ◽  
pp. 1227-1235
Author(s):  
Nguyen Truong Son ◽  
Jan Lasovský ◽  
Eduard Ružička

In weakly acidic medium, pH 3.5-6.5, the title dye forms with aluminium ions a complex with the Al : L ratio 1 : 1. In the presence of cetylpyridinium or carbethoxypentadecyltrimethylammonium, ternary complexes AlL3Sr (r = 6 or 9, respectively) are formed. The equilibrium constants of the complexing equilibria in the binary and ternary systems concerned were calculated, and a method of photometric determination of aluminium has been suggested.


2001 ◽  
Vol 24 (2) ◽  
pp. 215-228 ◽  
Author(s):  
Hong-Zhen Lian ◽  
Shu-Ping Bi ◽  
Yi-Jun Chen ◽  
Lei-Mei Dai ◽  
Mi Cao ◽  
...  

2017 ◽  
Vol 431 ◽  
pp. 34-47 ◽  
Author(s):  
Amieibibama Joseph ◽  
Christine M. Sands ◽  
Peter D. Hicks ◽  
Howard W. Chandler

2008 ◽  
Vol 44 (1) ◽  
pp. 49-61 ◽  
Author(s):  
Ana Kostov ◽  
B. Friedrich ◽  
D. Zivkovic

Thermodynamic calculations of three binary Ti-based alloys: Ti-Al, Ti-Fe, and Al-Fe, as well as ternary alloy Ti-Al-Fe, is shown in this paper. Thermodynamic calculations involved thermodynamic determination of activities, coefficient of activities, partial and integral values for enthalpies and Gibbs energies of mixing and excess energies at different temperatures: 1873K, 2000K and 2073K, as well as calculated phase diagrams for the investigated binary and ternary systems. The FactSage is used for all thermodynamic calculations.


2014 ◽  
Vol 33 (2) ◽  
pp. 209 ◽  
Author(s):  
Leposava Pavun ◽  
Predrag Đurđević ◽  
Milena Jelikić-Stankov ◽  
Daniela Đikanović ◽  
Andrija Ćirić ◽  
...  

<p><span style="font-size: medium;"><span style="font-family: Times New Roman;">The simple, accurate and precise method based on fluorescence properties of aluminium (III)–quercetin complex, for the determination of quercetin has been developed and validated. The complex has strong emission at pH 3.30, </span><em>l</em></span><span style="font-family: Times New Roman;"><span style="font-size: small;"><em><sub>em</sub></em></span><span style="font-size: medium;"> = 480 nm, with </span></span><span style="font-size: medium;"><em>l</em></span><span style="font-family: Times New Roman;"><span style="font-size: small;"><em><sub>ex</sub></em></span><span style="font-size: medium;"> = 420 nm</span><span style="font-size: medium;">. Linearity range of quercetin determination was 1.5 - 60.5 ng mL</span><sup><span style="font-size: small;">-1</span></sup><span style="font-size: medium;"> with LOD 0.09 ng mL</span><sup><span style="font-size: small;">-1</span></sup><span style="font-size: medium;"> and LOQ 0.27 ng mL</span><sup><span style="font-size: small;">-1</span></sup><span style="font-size: medium;">. Recovery values in the range of 99.9 – 100.2 % indicate a good accuracy of the method. The established method was applied for the determination of quercetin in capsules, with </span><span style="font-size: medium;">Recovery value<strong> </strong>98.3 %, standard deviation 0.22 <strong>% </strong>and<strong> </strong>coefficient of variation<strong> </strong>0.09<strong> %</strong>.<strong> </strong></span></span></p><p>  The reliability of the method was checked by RP-HPLC/UV method for capsules with direct determination of quercetin after separation. The good agreement between two methods indicates the applicability usability of the proposed spectroflurometric method for quercetin determination in pharmaceutical dosage forms, with high reproducibility, and enables direct and simple determination without its prior extraction from samples.</p><p>The proposed spectrofluorimetric method has much better sensitivity and about 1000 times lower <em>LOD</em> and <em>LOQ</em> values compared to data reported in literature.</p>


2010 ◽  
Vol 93 (6) ◽  
pp. 1821-1828 ◽  
Author(s):  
Alaa El-Gindy ◽  
Mohammed Wafaa Nassar ◽  
Nasr Mohammed El-Abasawy ◽  
Khalid Abdel-Salam Attia ◽  
Maisra Al-Shabrawi

Abstract A simple, selective, sensitive, accurate, and precise method was developed for determination of metformin hydrochloride (MF) in human urine using RP-HPLC. The method depends upon using an octylsilyl (C8) 5 m particle size column at ambient temperature with mobile phase consisting of 33 mM sodium dihydrogen phosphate containing 6.38 mM hexanesulfonic acid sodium salt and adjusted to apparent pH 3.0 with phosphoric acidacetonitrile (93 7, v/v) at a flow rate of 1.5 mL/min. Quantitation was achieved with UV detection at 231 nm based on peak area with a linear calibration curve over the concentration range of 0.0150 g/mL. The proposed method was applied to the determination of the urinary excretion pattern of MF (the cumulative amounts excreted were calculated without pretreatment of the urine sample) and for determination of the dissolution pattern of MF tablets. The proposed method was completely validated according to the U.S. Food and Drug Administration guidelines.


Author(s):  
Kadakanchi Sandeepa ◽  
Tulasi S.V.R. Neeharika ◽  
Ravi Kumar K ◽  
Bankupalli Satyavathi ◽  
Prathap Kumar Thella

1961 ◽  
Vol 41 (4) ◽  
pp. 380-384 ◽  
Author(s):  
Arthur F. Dratz ◽  
James C. Coberly
Keyword(s):  

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