Voltammetric studies of the Co(II)-tris(hydroxymethyl)aminomethane and sodium perborate volumetric catalytic system

2009 ◽  
Vol 74 (11-12) ◽  
pp. 1715-1725 ◽  
Author(s):  
Jerzy Zarębski ◽  
Andrzej Bobrowski ◽  
Agnieszka Królicka ◽  
Maria Putek

It has been shown that in the tris(hydroxymethyl)aminomethane (THAM)/HCl buffer, Co(II) ions catalyze the oxidation of THAM by sodium perborate. The reaction occurs at boiling temperature, and the product of the catalytic THAM oxidation, tris(hydroxymethyl)nitrosomethane, gives a well-defined quasireversible cathodic wave preceding that of the Co(II) ions by about 160 mV. The voltammetric responses of this product are proportional to the amount of sodium perborate and to the concentration of Co(II) ions. In the volumetric catalytic system of Co(II) ions/THAM/sodium perborate, the sensitivity of the determination of Co(II) is increased by one to two orders of magnitude, depending on the voltammetric technique used. Prior to the detection of tris(hydroxymethyl)nitrosomethane, EDTA was added to the solution to form voltammetrically inactive complexes with Co(II) and other interfering ions. Therefore, this method may be applied for the determination of Co(II) ions at low concentrations in the presence of a large excess of interfering ions, in particular Ni(II) and Zn(II).


Molecules ◽  
2021 ◽  
Vol 26 (4) ◽  
pp. 813
Author(s):  
Magdalena Świądro ◽  
Paweł Stelmaszczyk ◽  
Irena Lenart ◽  
Renata Wietecha-Posłuszny

The purpose of this study was to develop and validate a high-sensitivity methodology for identifying one of the most used drugs—ketamine. Ketamine is used medicinally to treat depression, alcoholism, and heroin addiction. Moreover, ketamine is the main ingredient used in so-called “date-rape” pills (DRP). This study presents a novel methodology for the simultaneous determination of ketamine based on the Dried Blood Spot (DBS) method, in combination with capillary electrophoresis coupled with a mass spectrometer (CE-TOF-MS). Then, 6-mm circles were punched out from DBS collected on Whatman DMPK-C paper and extracted using microwave-assisted extraction (MAE). The assay was linear in the range of 25–300 ng/mL. Values of limits of detection (LOD = 6.0 ng/mL) and quantification (LOQ = 19.8 ng/mL) were determined based on the signal to noise ratio. Intra-day precision at each determined concentration level was in the range of 6.1–11.1%, and inter-day between 7.9–13.1%. The obtained precision was under 15.0% (for medium and high concentrations) and lower than 20.0% (for low concentrations), which are in accordance with acceptance criteria. Therefore, the DBS/MAE/CE-TOF-MS method was successfully checked for analysis of ketamine in matrices other than blood, i.e., rose wine and orange juice. Moreover, it is possible to identify ketamine in the presence of flunitrazepam, which is the other most popular ingredient used in DRP. Based on this information, the selectivity of the proposed methodology for identifying ketamine in the presence of other components of rape pills was checked.



1959 ◽  
Vol 11 (1) ◽  
pp. 352-359 ◽  
Author(s):  
A. H. Beckett ◽  
S. J. Patki ◽  
Ann E. Robinson
Keyword(s):  




1968 ◽  
Vol 32 (4) ◽  
pp. 412-423
Author(s):  
Michinori Nakamura
Keyword(s):  


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