Use of less polar organic solvents for the polarographic determination of metals after extraction of their diethyldithiocarbamates

1992 ◽  
Vol 342 (9) ◽  
pp. 698-701 ◽  
Author(s):  
Yukio Nagaosa ◽  
Kiyoshi Horita ◽  
Seiichi Nishimoto
1982 ◽  
Vol 36 (4) ◽  
pp. 430-435 ◽  
Author(s):  
David K. Lavallee ◽  
Thomas J. McDonough ◽  
Lisa Cioffi

As part of an ongoing study of the chemistry and properties of N-methylporphyrins and their metal complexes, we have observed that the excitation and emission spectra of N-methyltetraphenylporphyrin and N-methyltetra( p-sulfophenyl)porphyrin and their zinc complexes closely resemble corresponding spectra of chlorophyll a. We have characterized fluorescence spectra for these species in a variety of solvents commonly used for quantitative determination of chlorophylls. Quantum yields for the N-methylporphyrins are lower by approximately a factor of 10 than yields for chlorophyll a in such solvents as acetone, ethanol, and mixed aqueous/organic solvent systems. The yields are quite sufficient, however, for these species to be used as fluorescence standards. Solution of N-methylporphyrins are stable and the compounds can be inexpensively synthesized in high purity. The tetra( p-sulfophenyl) species are soluble in aqueous and highly polar organic solvents, whereas the tetraphenyl species are soluble in nonpolar organic solvents.


1960 ◽  
Vol XXXV (I) ◽  
pp. 34-48 ◽  
Author(s):  
Gerd Ittrich

ABSTRACT A series of organic solvents and phenol derivatives have been examined for the extraction of the pink Kober-colour complex. Optimal results could be achieved for fluorimetry by a solution of 2 % (w/v) p-nitrophenol and 1 % (v/v) ethanol in acetylenetetrabromide, when the green mercury line (546 mμ was used as primary light. The sensitivity, stability and specificity have been improved, compared with the previously described reaction. By changing the sequence of purification steps and by reducing the volume of the urine sample (5 ml) the method for the determination of total oestrogens has been simplified. Approximately 10 determinations can be done within 3–4 hours by one person. Recovery experiments and comparative determinations with a previously described method have been carried out. The excretion of total oestrogens in a complete menstrual cycle is determined with the described method.


2014 ◽  
Vol 32 (11) ◽  
pp. 1251
Author(s):  
Jing DA ◽  
Xianglu HUANG ◽  
Gangli WANG ◽  
Jin CAO ◽  
Qingsheng ZHANG

1987 ◽  
Vol 52 (3) ◽  
pp. 609-615
Author(s):  
A. Díaz ◽  
S. González ◽  
A. Arévalo

The minimum on the polarographic curves for Bi(III) reduction in HCl solutions occurring when small amounts of surfactants are present can be used for their quantitative determination. The form of the polarograms was examined with respect to the concentration of the surfactant, and the range of concentrations in which the method of determination can be used is discussed.


1959 ◽  
Vol 31 (7) ◽  
pp. 1217-1219 ◽  
Author(s):  
R. E. Van Atta ◽  
D. R. Jamieson

Author(s):  
Aradhya Dev Srivastav ◽  
Vireshwar Singh ◽  
Deepak Singh ◽  
Balendu Shekher Giri ◽  
Dhananjay Singh

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