Based on acetylacetone a new organic reagent was synthesized. Its crystal structure was studied. Its complexation with copper was Studied by spectrophotometric method. The effect of the third component on the complexation of Cu-R was considered. The composition of the reactants was studied by different physico-chemical methods. The effect of foreign ions on complexation was studied. The technique was applied to the determination of trace amounts of copper in natural objects.
The influence of sorption characteristics on the removal of silver(I) has been examined. The sorption capacity of chelating polymeric sorbent, based on maleic anhydride styrene copolymer modified with m-aminophenol, towards Ag(I) ions was studied. The pH of sorption was maximum at the value 6. With the increasing of initial metal concentration, sorption of silver(I) increases and reached maxima at val-ue 80∙10-3 M. At the final stage, the elution process of Ag(I) was established and find that HNO3 1 M is the best elution agent. Multiple use of the regenerated sorbent for sorption process is possible. This study shows that using of mentioned sorbent modified with m-aminophenol is effective for removal of silver(I) ions from aqueous solutions
A modified sorbent based on copolymer of maleic anhydride with methacrylic acid was proposed for sorption of vanadium (V) concentration. A polymer chelating sorbent with fragments of para-amino salicylic acid was used in the work. Optimal sorption conditions were determined and the dependence of sorption capacity on the acidity of the solution studied. At pH 5, the degree of sorption attains its maximum. The effect of ionic strength on vanadium sorption was studied. Studies have shown that the ionic strength up to 0.6 mol/l does not affect the sorption, after 0.6 mol/l the increase in the ionic strength at the beginning gradually, and then sharply decreases the sorption. The effect of ionic strength on vanadium sorption was studied to show that the ionic strength up to 0.6 mol/l does not affect the sorption, and after 0.6 mol/l the increase in the ionic strength at the beginning gradually, and then sharply decreases the sorption. All further experiments were carried out in the solutions with an ionic strength of 0.6. It was found that as the concentration of vanadium rises in the solution, the amount of sorbed metal increases, and at a concentration of 8.10-3 mol/l it becomes maximum (pH = 5, CV5+ = 8.10-3 mol/l, vtotal = 20 ml, msorb. = 0.03 g, SC = 243 mg/g). The isotherm of vanadium (V) sorption with the synthesized sorbent was constructed. Sorption equilibrium is achieved within 1 hour of contact between the solution and the sorbent. Further growth in the sorption time does not change sorbent’s characteristics. The sorbent extracts vanadium (V) from solutions with a recovery rate of 93%. The effect of different mineral acids (HClO4, H2SO4, HNO3, HCl) of identical concentrations on vanadium (V) desorption from the sorbent was also studied. The results of the analysis showed that the maximum desorption of vanadium (V) occurs in perchlorate acid. The developed method was applied to determine the trace amounts of vanadium in oil sludge with preliminary concentration.
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