Sorption of magnesium–picolinate complexes on a macroporous styrene–divinylbenzene copolymer containing immobilized 8-hydroxyquinoline and on the copolymer itself

1992 ◽  
Vol 70 (3) ◽  
pp. 926-930 ◽  
Author(s):  
Gocool Persaud ◽  
Frederick F. Cantwell

The sorbent XAD-OXINE was prepared by covalently binding 8-hydroxyquinoline onto the surface of the macroporous copolymer Amberlite XAD-2 to give about 20% surface coverage. Sorption, onto both XAD-2 and XAD-OXINE, of the magnesium-containing species that are present in solutions of magnesium ion and picolinic acid was studied by the column equilibration/atomic absorption technique at solution pH of 6.00 and 7.50 and ionic strength of 0.25. By using solutions containing various amounts of added magnesium and picolinic acid, in which the ratio of the two metal–ligand complex species, MgP+/MgP2, varied greatly (P− is the ligand picolinate), it was shown that neither the species Mg2+ nor the species MgP+ sorb to an appreciable extent onto the parent polymer XAD-2, but the neutral species MgP2 sorbs strongly and exhibits a linear isotherm. Then, by measuring the sorption isotherm of the species Mg2+ on XAD-OXINE in the absence of picolinic acid, by measuring the overall sorption of magnesium-containing species on XAD-OXINE in the presence of picolinic acid, and by assuming that the sorption of the species MgP2 onto XAD-OXINE was about the same as it was on XAD-2, it was possible to show that the species MgP+ sorbs strongly onto XAD-OXINE, and exhibits linear sorption isotherms. Thus, XAD-OXINE sorbs all three species Mg2+, MgP+, and MgP2. Keywords: Amberlite XAD-2, immobilized oxine, magnesium ion.

1975 ◽  
Vol 21 (4) ◽  
pp. 558-561 ◽  
Author(s):  
Frank J Fernandez

Abstract I describe a micro-scale method for determining lead in whole blood by utilizing a graphite furnace. Sample pretreatment consists of fivefold dilution with a dilute surfactant. The method is directly calibrated with lead standards prepared in dilute HNO3. To eliminate a small, nonspecific absorption signal from the blood matrix, simultaneous background correction is used. Interlaboratory comparison with a flame atomic absorption technique that requires extraction yielded high correlation (r = 0.98). Within-run precision (coefficient of variation) ranged from 2 to 4%. Lead in blood can be accurately measured in as little as 20 µl of blood, hence the method is suitable for routine laboratory use and for pediatric screening.


1975 ◽  
Vol 29 (1) ◽  
pp. 44-48 ◽  
Author(s):  
J. A. Goleb ◽  
C. R. Midkiff

A flameless atomic absorption technique, employing a tantalum strip atomizer, has been developed to determine barium and antimony in gunshot residue. Cotton swabs, wetted with 5% HNO3, are used to collect residue. Barium and antimony are released from the swabs by acid leaching or plasma ashing. Both techniques give good recoveries; the ashing technique is preferred for blood-stained swabs. The sensitivity for barium is 0.1 ng/10 µl and antimony 0.2 ng/10 µl. At nanogram levels the standard relative deviation for barium is 8.3% and for antimony 8.5%.


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