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1.
Ion exchange equilibria
in simultaneous extraction of platinum(II, IV) and
rhodium
(III) from hydrochloric solutions / A. M. Mel'nikov [et al.]> // Russ. J. Phys. Chem. A. - 2012. -
Vol. 86
,
Is. 6
. - P. 1018-1024,
DOI
10.1134/S0036024412060192. - Cited References: 24 . - ISSN 0036-0244
РУБ
Chemistry, Physical
Кл.слова (ненормированные):
platinum
--
rhodium
--
ionites
--
ion exchange equilibria
--
hydrochloric acid solutions
--
sorption
Аннотация:
Regularities of sorption extraction of platinum(II, IV) and
rhodium
(III) by anion exchangers of various physical and chemical structure in the presence of hydrochloric media were studied. It is established that AM-2B, Purolite A 500, and Purolite S 985 ionites adsorb complex anions of platinum metals employing mixed mechanism. A high affinity of the studied anionites for the studied complex anions of platinum and
rhodium
is established.
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Публикация на русском языке
Ионообменные равновесия при совместном извлечении платины (II, IV) и родия (III) из солянокислых растворов [Текст] / А. М. Мельникова [и др.] // Журн. физ. химии. - 2012. - Т. 86 № 6. - С. 1129-1135
Держатели документа:
[Mel'nikov, A. M.] Siberian Fed Univ, Inst Nonferrous Met & Mat Sci, Krasnoyarsk 660041, Russia
[Kononova, O. N.
Pavlenko, N. I.] Russian Acad Sci, Inst Chem & Chem Technol, Siberian Branch, Krasnoyarsk 660049, Russia
[Krylov, A. S.] Russian Acad Sci, LV Kirensky Phys Inst, Krasnoyarsk 660036, Russia
Доп.точки доступа:
Mel'nikov, A. M.; Kononova, O. N.; Pavlenko, N. I.; Krylov, A. S.; Крылов, Александр Сергеевич
}
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2.
Ion-exchange extraction of
platinum(II,IV) from chloride solutions in the presence of iron(III) / O. N. Kononova [et al.]> // Russ. J. Phys. Chem. A. - 2015. -
Vol. 89
,
Is. 8
. - P. 1464-1470,
DOI
10.1134/S0036024415080166. - Cited References: 28 . - ISSN 0036-0244. - ISSN 1531-863X
РУБ
Chemistry, Physical
Рубрики:
RHODIUM
Кл.слова (ненормированные):
platinum
--
iron
--
ionites
--
sorption
--
hydrochloric solutions
--
sorption
Аннотация:
The sorption concentration of platinum(II,IV) in the presence of iron(III) is studied on new samples of domestically produced ionites of the CYBBER brand. In comparing the sorption and kinetic properties of the new ionites to those of sorbents of the Purolite brand studied earlier, the higher effectiveness of the former is demonstrated via the extraction of platinum(II,IV) ions from strongly and weakly acidic chloride solutions. It is found that the sorbed platinum ions can be completely separated from iron(III) ions through separate elution using 0.01-0.001 M HCl (iron ions) and a thiourea solution (80 g/L) in 0.3 M H2SO4 (platinum ions).
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Публикация на русском языке
Ионообменное извлечение платины (II, IV) в присутствии железа (III) из хлоридных растворов [Текст] / О. Н. Кононова [и др.] // Журн. физ. химии : Наука, 2015. - Т. 83 № 8. - С. 1305-1312
Держатели документа:
Institute of Nonferrous Metals and Materials Science, Siberian Federal University, Krasnoyarsk, Russian Federation
Kirensky Institute of Physics, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, Russian Federation
Доп.точки доступа:
Kononova, O. N.; Duba, E. V.; Karplyakova, N. S.; Krylov, A. S.; Крылов, Александр Сергеевич
}
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3.
Rhodium
(III) speciation in
concentrated nitric acid solutions / D. Vasilchenko [et al.]> // Eur. J. Inorg. Chem. - 2016. -
Vol. 2016
,
Is. 23
. - P. 3822-3828,
DOI
10.1002/ejic.201600523. - Cited References:31. - This work was supported by the Russian Foundation for Basic Research (grant number 16-03-00549 A). D. V. thanks the Ministry for Education and Science of the Russian Federation for the award of a President of the Russian Federation for Young Scientists Fellowship. . - ISSN 1434-1948. - ISSN 1099-0682
РУБ
Chemistry, Inorganic & Nuclear
Рубрики:
MAGNETIC-RESONANCE
FISSION PLATINOIDS
AQUEOUS-SOLUTIONS
PT-195 NMR
RH(III)
SPECTROSCOPY
CHEMISTRY
DISSOCIATION
PLATINUM(IV)
COMPLEXES
Кл.слова (ненормированные):
Rhodium
--
NMR spectroscopy
--
Nitrates
Аннотация:
The interaction of
rhodium
(III) aqua ions with nitrate ions in 3–16 m nitric acid solutions has been studied by 103Rh and 15N NMR and Raman spectroscopy. The mononuclear complexes [Rh(H2O)6–n(NO3)n]3–n (n = 1–4) were found to be the only form of
rhodium
(III) existing in the solutions with the metal concentration in the range 0.2–1.3 m. The dynamics of the H2O → NO3– substitution process was studied at 80 °C. An increase in the average number of nitrate groups bonded to
rhodium
with increasing concentration of nitric acid was also determined. The fine crystalline salt Rb4trans-[Rh(H2O)2(NO3)4][Rh(NO3)6] was obtained by solvothermal concentration of the
rhodium
nitric acid solution on addition of rubidium nitrate. The structure of the salt was solved by the powder X-ray diffraction method, with monodentate coordination of nitrato ligands found for both the [Rh(NO3)6]3– and trans-[Rh(H2O)2(NO3)4]– anions.
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Держатели документа:
Russian Acad Sci, Nikolaev Inst Inorgan Chem, Siberian Branch, Novosibirsk 630090, Russia.
Novosibirsk State Univ, Novosibirsk 630090, Russia.
RAS, Inst Chem & Chem Technol, SB, Krasnoyarsk 660049, Russia.
RAS, Kirensky Inst Phys, SB, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, 79 Svobodny Pr, Krasnoyarsk 660041, Russia.
Доп.точки доступа:
Vasilchenko, D.; Vorob'eva, S.; Tkachev, S.; Baidina, I. A.; Belyaev, A.; Korenev, S.; Solovyov, L.; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Russian Foundation for Basic Research [16-03-00549 A]; Ministry for Education and Science of the Russian Federation
}
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4.
Simultaneous ion exchange
recovery of platinum and
rhodium
from chloride solutions / O. N. Kononova [et al.]> // Hydrometallurgy. - 2011. -
Vol. 105
,
Is. 3-4
. - P. 341-349,
DOI
10.1016/j.hydromet.2010.11.009. - Cited Reference Count: 46 . - JAN. - ISSN 0304-386X
Рубрики:
GROUP-METALS PGM
SEPARATION
CATALYST
ANION
ADSORPTION
EXTRACTION
CHEMISTRY
RESIN
Кл.слова (ненормированные):
platinum
--
rhodium
--
sorption
--
anion exchangers
--
chloride solutions
--
anion exchangers
--
chloride solutions
--
platinum
--
rhodium
--
sorption
--
ammonium thiocyanate
--
anion exchangers
--
basic parameters
--
chemical structure
--
chloride solutions
--
diffusion coefficients
--
distribution coefficient
--
exchange capacities
--
kinetic properties
--
noble metals
--
purolite
--
rhodium
chloride
--
separation factors
--
sorption ability
--
work focus
--
ammonium compounds
--
chlorine compounds
--
desorption
--
hydrochloric acid
--
ion exchange
--
ion exchange resins
--
ions
--
platinum
--
platinum compounds
--
potassium hydroxide
--
precious metals
--
recovery
--
rhodium
--
sulfuric acid
--
thioureas
--
urea
--
rhodium
compounds
Аннотация:
This work focuses on the sorption recovery of platinum (II, IV) and
rhodium
(III) simultaneously present in chloride solutions, freshly prepared and stored over 3 months, on commercial anion exchangers with different physical and chemical structure. The sorption was carried out from solutions with 0.001-4.0 mol/L HCl. The initial platinum and
rhodium
concentrations in contacting solutions were 0.25-2.5 mmol/L Sorption and kinetic properties of the chosen anion exchangers were investigated and the basic parameters of exchange capacity, recovery, distribution coefficients, separation factors, process rate, diffusion coefficients and half-exchange times were calculated. It is shown that anion exchangers investigated possess high sorption ability to platinum and
rhodium
chloride complexes, which does not deteriorate in case of stored solutions. Desorption of platinum and
rhodium
from the resins investigated was carried out with hydrochloric acid (2 mol/L), thiourea (1 mol/L) in sulfuric acid (2 mol/L) or in potassium hydroxide (2 mol/L) as well as by ammonium thiocyanate (2 mol/L). It was shown that complete separation of platinum and
rhodium
can be carried out with 2 mol/L HCl on anion exchanger Purolite S 985, whereas 2 mol/L NH(4)SCN as an elution agent leads to complete separation of noble metals on anion exchangers Purolite S 985, Purolite A 500 and AM-2B. (C) 2010 Elsevier B.V. All rights reserved.
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Держатели документа:
Siberian Fed Univ, Dept Chem, Krasnoyarsk 660041, Russia
Russian Acad Sci, LV Kirensky Phys Inst, Siberian Dept, Krasnoyarsk 660036, Russia
Доп.точки доступа:
Kononova, O.N.; Melnikov, A.M.; Borisova, T.V.; Krylov, A. S.; Крылов, Александр Сергеевич
}
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5.
Structure, UV spectroscopic
and electrochemical properties of 2-methyl-8-quinolinolato
rhodium
(I) complexes, containing carbonyl, triphenylphosphine or triphenylphosphite ligands / V. V. Verpekin, A. D. Vasiliev, N. G. Maksimov [et al.]> // J. Mol. Struct. - 2022. -
Vol. 1249
. - Ст. 131557,
DOI
10.1016/j.molstruc.2021.131557. - Cited References: 31. - This work was conducted within the framework of the budget project # 121031500209-6 for Institute of Chemistry and Chemical Technology SB RAS using the equipment of Krasnoyarsk Regional Research Equipment center of Federal Research center, SB RAS. Authors are grateful to Alexander A. Kondrasenko for NMR measurements . - ISSN 0022-2860
Кл.слова (ненормированные):
Rhodium
--
2-methyl-8-quinolinolate
--
Carbonyl
--
Triphenylphosphine
--
Triphenylphosphite
--
Electrochemistry
--
UV spectroscopy
--
X-ray structure
Аннотация:
The known Rh(2-Me-8-Oxq)(CO)2 complex (1) was prepared through treatment of dicarbonyl(acetylacetonate)
rhodium
(I) with 2-methyl-8-hydroxyquinoline for the first time. The reactions of 1 with triphenylphosphine and triphenylphosphite result in complexes Rh(2-Me-8-Oxq)(PPh3)(CO) (2) and Rh(2-Me-8-Oxq)[P(OPh)3](CO) (3) that were characterized by IR and NMR spectroscopy. The structures of complexes 2 and 3 were determined by single-crystal X-ray diffraction analysis. The complexes show the 2-methyl-8-quinolinolato ligand in the expected coordination mode with a slightly disordered square planar geometry at the
rhodium
center. In the crystal, molecules of Rh(2-Ме-8-Oxq)(CO)(PPh3) (2) form centrosymmetric dimers due to π-stacking interactions. No intermolecular contacts are observed in the crystal of 3. The UV spectroscopic and electrochemical properties of complexes 1–3 were studied. Their electronic spectra in CH3CN show three quinoline-centered absorptions. The electrochemical study revealed that the oxidation of the complexes 1–3 is two-electron and leads to the formation of dication Rh (III) species while their reduction gives radical anions, which undergoes rapid decomposition.
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Держатели документа:
Institute of Chemistry and Chemical Technology SB RAS, Federal Research Center “Krasnoyarsk Science Center SB RAS”, Akademgorodok, 50-24, Krasnoyarsk, 660036, Russian Federation
Institute of Physics SB RAS, Federal Research Center “Krasnoyarsk Science Center SB RAS”, Akademgorodok, 50-38, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Svobodny Prospect, 79, Krasnoyarsk, 660041, Russian Federation
Доп.точки доступа:
Verpekin, V. V.; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Maksimov, N. G.; Burmakina, G. V.; Zimonin, D. V.; Nedelina, T. S.; Chudin, O. S.; Rubaylo, A. I.
}
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