Fluorescence characteristics of Rauwolfia alkaloids in highly concentrated sulphuric acid solutions. Fluorimetric determination of reserpiline

1986 ◽  
Vol 4 (4) ◽  
pp. 505-509 ◽  
Author(s):  
M. Balón-Almeida ◽  
M.A. Muñoz-Perez ◽  
J. Hidalgo-Toledo ◽  
M. Sánchez-González
1960 ◽  
Vol 38 (12) ◽  
pp. 2488-2492 ◽  
Author(s):  
D. E. Ryan

Zirconium is completely precipitated by benzoylphenylhydroxylamine from 0.5 N acid solutions. The complex formed in sulphuric acid solutions has a constant composition, Zr(C13H10O2N)4, and is used for the direct weighing of zirconium; the factor is 0.0970. The product precipitated from hydrochloric acid solutions must be ignited to the oxide. The reaction is sensitive, 1 p.p.m. of zirconium being detectable, and quantitative determination of 0.2 mg is possible. Thorium and the rare earths do not interfere.


1979 ◽  
Vol 57 (9) ◽  
pp. 974-981 ◽  
Author(s):  
Eugene M. L. Valeriote ◽  
Lloyd D. Gallop ◽  
Pedro J. Aragon

Measurements of the solubility of lead sulphate in 35% by weight sulphuric acid, pure water, and at two intermediate acid concentrations have been made over the temperature range 25 °C to −50 °C using differential pulse anodic stripping voltammetry.Values of the standard enthalpy of solution, derived from the data and from that of other workers, have been found to be higher than those obtained from emf measurements. The extent of lead sulphate ion pairing is analyzed at 25 °C and discussed. The slowness of equilibration of acid solutions supersaturated with lead sulphate was judged of importance in deciding the relevance of the use of thermodynamically calculated lead ion concentrations with respect to lead acid battery mechanisms.


1989 ◽  
Vol 54 (3) ◽  
pp. 616-621 ◽  
Author(s):  
Záviš Holzbecher

It has been found that phosphoric acid decreases the first excitation maximum of Ce(III) at 256 nm, increases the second excitation maximum at 297 nm and shifts the fluorescence maximum from 350 to 346 nm. Under optimum conditions, with λexc = 297 nm and λem = 346 nm, Ce(III) can be determined fluorimetrically with a detection limit of 1.2 ng ml-1 in 12M-H3PO4 medium. No interference was observed from a 20-200 fold excess of HCl, H2SO4, Na, K, NH4+, Al and the rare earth elements. HNO3 interferes and Ce(IV) and Fe(III) interfere strongly. It follows from the stereofluorograms of Ce and Tb that the spectra of the two elements are practically independent. The detection limit for Tb(III) in 0.02-2.5M-H2SO4 medium for λexc = 222 nm and λem = 494 nm is 33 ng ml-1. No interference was observed from a 5-20 fold excess of Al3+ and the other rare earth elements. The determination is slightly less sensitive in H3PO4 or HCl medium. The relative standard deviation of the measurement for 10 ng ml-1 Ce(III) or 50 ng ml-1 Tb(III) is about 3%.


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