Interphase distribution of palladium(II) different-charged chloride complexes in extraction systems based on liquid anion exchangers
Abstract
The extraction of palladium(II) different-charged chloride acid complexes was investigated depend- ing on structure of the liquid anion exchanger in chloroform and the concentration of ligand. Extractants 0.1 M solutions of primary alkylamine nitrates were studied (using n-dodecylammonium as an example), extrac- tants tertiary alkylamines were also used (dimethyl-n-dodecylammonium and tri-n-octylammonium (TOA) as an examples). The differentiation of the extraction behavior of liquid anion exchangers of various structures during the extraction of palladium(II) mixed-charge chloride complexes has been established. In concentrated chloride solutions with a ratio of [Pd2+] /[Cl–] = 1:1700, where [PdCl4]2– is in equilibrium with high charged acid complexes (HCAC) [PdCl5]3–, [PdCl6]4–, the behavior of 4-n-dodecylammonium and dimethyl-n- dodecylammonium is approximately equivalent (R = 74 and 68%).
Higher degree of extraction compared with three-n-octylammonium (R = 28%) is observed for these extractants. The reducing of tertiary alkylamine radicals volume by replacing of two alkyl radicals with me- thyl ones makes it possible to reduce steric factors and to use different-radicals tertiary alkylamines to extract HCAC of palladium(II) that was not previously used for these purposes. An increase in the concentration of the extractant dimethyl-n-dodecylammonium to 0.2 mol / dm3 leads to the complete extraction of the analyte. In the system with the ratio [Pd2+] / [Cl–] = 1:4 TOA extracts palladium(II) by 58% from the aqueous phase. The separation of anionic forms of palladium in chloride solutions was established by extraction and molecu- lar absorption spectrophotometry. The absorption maximum of palladium associates with n- dodecylammonium and dimethyl-n-dodecylammonium in the extracts and the aqueous phase is at λ = 470nm. In the absorption spectrum of TOA associate with a maximum is observed at λ = 430 nm, which is a cha- racteristic of low-charged acid complex. The composition [C12H25(CH3)2NH]3PdCl5 of palladium(II) asso- ciate with dimethyl n-dodecyammonium in the organic phase was established by the methods of equilibrium shift and molecular absorption spectrophotometry.
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References
2. Shevchuk I.A., Simonova T.N. Jekstrakcija soedinenij cvetnyh i redkih metallov iz karbonatnyh, serusoderzhashhih i galogenidnyh rastvorov, Donetsk, DonGU, 1999, 215 p.
3. Simonova T.N., Gontar E.S., Sorbtsionnye i Khromatograficheskie Protsessy. 2017, Vol. 17, No 4, рр. 585-591.
4. Ginzburg S.I. et al. Analiticheskaja himija platinovyh metallov. M., Nauka, 1972, 613 p.
5. Zolotov Yu.A., Varshal G.M., Ivanov V.M. Analiticheskaja himija metallov platinovoj gruppy: Sb. obzornyh statej. Moscow, Editorial URSS, 2003, 592 p.
6. Livingston S. Himiya ruteniya, rodiya, pal- ladiya, osmiya, iridiya, platinyi. M., Mir, 1978, 366 р.
7. Sundaram A.K., Sandell E.B., J. Amer. Chem. Soc, 1955, Vol. 77, рр. 855−857.
8. Ginzburg S.I., Kiseleva N.V., ZHurn. neor- gan. khimii., 1958, Vol. 3, No 8, pp. 1804-1809.
9. Shevchuk I.A., Simonova T.N., Gontar E.S., Mezhdunarodnaya konferentsiya po himi- cheskoy tehnologii, June 17-23, 2007, M., 2007, p. 227.
10. Marchenko Z., Baltsezhak M. Metodyi spektrofotometrii v UF i vidimoy oblastyah v neorganicheskom analize. Moscow, BINOM. Laboratoriya znaniy, 2007, 711 p.