Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Wyszukujesz frazę "Solvent extraction" wg kryterium: Wszystkie pola


Tytuł:
Nickel-cobalt separation by solvent extraction method
Autorzy:
Radzyminska-Lenarcik, E.
Wasilewska, A.
Powiązania:
https://bibliotekanauki.pl/articles/115651.pdf
Data publikacji:
2015
Wydawca:
Fundacja na Rzecz Młodych Naukowców
Tematy:
separation ions
solvent extraction
cobalt(II)
nickel(II)
alkylimidazole
separacja jonów
ekstrakcja rozpuszczalnikowa
kobalt(II)
nikiel(II)
alkiloimidazol
Opis:
Separation of cobalt(II), and nickel(II) ions from nitrate solutions using liquid-liqiud extraction process was reported. The measurements were run at 25oC and at fixed ionic strength equal to 0.5 (KNO3,HNO3). Initial concentrations of Co(II) and Ni(II) nitric acid in the aqueous phase were constant (0.01 M and 0.15 M, respectively). Both 1-hexylimidazole (1), and 1-hexyl-2-methylimidazole (2), both in dichloromethane were used as extractants. Their concentrations in organic phase were varied from 0.01 to 0.25 M. Cobalt(II) in an aqueous solution forms both tetrahedral and octahedral complexes. Nickel(II) forms only a six-coordinate complexes. These general differences help to provide the basis for the various separation processes currently used for cobalt-nickel separation. The steric effect for extractant 2 facilitates the extraction of tetrahedral Co(II) complexes. Extraction percent (%E) of cobalt(II) and nickel(II) in the systems studied were calculated. The percentage extraction increases for increasing values of pH of aqueous phase and is the highest for pH = 7.2. In the aqueous phase, of which the pH = 7.2, there remain 75%Ni(II) and 40% Co(II) for extractant 1 and the respective values for extractant 2 are 85% Ni(II) and 20% Co(II). The steric effect increases selectivity coefficients Co(II)/Ni(II). The highest selectivity coefficients for both extractants were obtained at a pH of aqueous phase = 6.2; their values were 5 and 8.9 for extractants 1 and 2, respectively.
Źródło:
Challenges of Modern Technology; 2015, 6, 3; 20-23
2082-2863
2353-4419
Pojawia się w:
Challenges of Modern Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Separation of lanthanides using micro solvent extraction system
Autorzy:
Nishihama, S.
Tajiri, Y.
Yoshizuka, K.
Powiązania:
https://bibliotekanauki.pl/articles/346897.pdf
Data publikacji:
2006
Wydawca:
Politechnika Bydgoska im. Jana i Jędrzeja Śniadeckich. Wydział Technologii i Inżynierii Chemicznej
Tematy:
micro solvent extraction
separation
light lanthanide
middle lanthanide
Opis:
A micro solvent extraction system for the separation of lanthanides has been investigated. The micro flow channel is fabricated on a poly(methyl methacrylate) (PMMA) plate, and solvent extraction progresses by feeding aqueous and organic solutions into the channel simultaneously. The extraction equilibrium is quickly achieved, without any mechanical mixing, when a narrow channel (100 µm width and 100 µm depth) is used. The results of solvent extraction from the Pr/Nd and Pr/Sm binary solutions revealed that both lanthanides are firstly extracted together, and then, the lighter lanthanide extracted in the organic solution alternatively exchanges to the heavier one in the aqueous solution to achieve the extraction equilibrium. The phase separation of the aqueous and organic phases after extraction can also be successively achieved by contriving the cross section of the flow channel, and the extractive separation of Pr/Sm is demonstrated.
Źródło:
Ars Separatoria Acta; 2006, 4; 18-26
1731-6340
Pojawia się w:
Ars Separatoria Acta
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Solvent extraction of copper(ii) from concentrated leach liquors
Autorzy:
Ochromowicz, K.
Chmielewski, T.
Powiązania:
https://bibliotekanauki.pl/articles/109873.pdf
Data publikacji:
2013
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
copper ore
hydrometallurgy
separation
Acorga
LIX
Opis:
Hydrometallurgical treatment of complex copper sulfidic ores, by-products and concentrates requires aggressive, oxidative leaching methods and application of Fe(III) ions and oxygen or bacteria assisted environment. Leach liquors generated in the process are usually copper and iron-rich solutions of high acidity. Such conditions require the application of suitably strong and selective reagent to extract copper in SX operations. This paper discusses the copper extraction behavior of commercial copper rea-gents: LIX 984N, LIX 612N-LV and Acorga M5640. Aqueous feed solutions used in SX studies were PLS’ generated in atmospheric leaching of commercial flotation concentrate, produced at Lubin Concen-trator (KGHM). McCabe-Thiele diagrams were generated and copper net transfer values were compared and discussed. It was shown that stronger modified aldoxime reagents (Acorga, LIX 612) are superior over non-modified salicylaldoxime/ketoxime mixture (LIX 984N). Particularly, the ester modified Acor-ga M5640 showed advantages in recovery and copper net transfer values.
Źródło:
Physicochemical Problems of Mineral Processing; 2013, 49, 1; 357-367
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
New approach for third phase investigation in solvent extraction system
Autorzy:
Borkowski, M.
Powiązania:
https://bibliotekanauki.pl/articles/346969.pdf
Data publikacji:
2008
Wydawca:
Politechnika Bydgoska im. Jana i Jędrzeja Śniadeckich. Wydział Technologii i Inżynierii Chemicznej
Tematy:
third phase
TBP
nitric acid
dodecane
solvent extraction
Opis:
The phenomenon of third phase formation in different liquid extraction systems is well known for more than 50 years but until now a good mathematical model that could predict the third phase formation has not been developed. The third phase is unwanted in extraction systems because, for example, in nuclear fuel reprocessing it can cause criticality problems. However, the third phase may be a useful tool in other technologies. In this paper a new approach to third phase investigation is proposed. This new approach eliminates the aqueous phase, simplifies the system and gives new insight in the nature the third phase. It is a step forward in understanding of the mechanism governing the formation of third phase. This new approach could quickly provide sufficient data to develop a comprehensive model.
Źródło:
Ars Separatoria Acta; 2008, 6; 31-40
1731-6340
Pojawia się w:
Ars Separatoria Acta
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Solvent extraction of zinc(II) ions from chloride media by 4-pyridylketoximes
Autorzy:
Parus, A.
Powiązania:
https://bibliotekanauki.pl/articles/410269.pdf
Data publikacji:
2016
Wydawca:
Uniwersytet Humanistyczno-Przyrodniczy im. Jana Długosza w Częstochowie. Wydawnictwo Uczelniane
Tematy:
solvent extraction
pyridylketoxime
zinc(II)
recovery
chloride media
Opis:
Three homologues of 4-pyridylketoximes were synthesized and used as potential ligands for zinc(II). Their solvent extraction behaviors for zinc(II) in chloride solutions were investigated using CHCl3 as the diluent. The effect of different variables on the extraction of zinc(II) ions, such as the pH of aqueous phase, metal and chloride ions as well as the type of oxime, has been investigated. Results indicated that 4-pyridylketoximes could extract zinc(II) ions from chloride solutions and the extraction depended on the concentrations of the ligand, chloride ions and hydrochloride acid. Slope analysis confirmed that the 4-pyridylketoximes ligands form a 1:2 complex with zinc(II) in both chloride/nitrate and chloride/perchlorate solutions. After extraction, zinc(II) could be easily stripped from organic phase with water.
Źródło:
Chemistry, Environment, Biotechnology; 2016, 19; 93-100
2083-7097
Pojawia się w:
Chemistry, Environment, Biotechnology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Lead(II) removal from aqueous solutions by solvent extraction with tetracarboxylresorcin[4]arene
Autorzy:
Konczyk, J.
Kozlowski, C.
Walkowiak, W.
Powiązania:
https://bibliotekanauki.pl/articles/110670.pdf
Data publikacji:
2013
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
solvent extraction
lead(II)
zinc(II)
cadmium(II)
resorcinarene
Opis:
A novel tetracarboxylresorcin[4]arene was synthesized and its selective complexing ability towards Pb(II) ions was examined. The influence of several parameters such as pH of aqueous phase, agitation time, extractant and modifier concentrations on solvent extraction of Pb(II) ions from the aque-ous nitrate phase into chloroform organic phase was studied. The stoichiometry of the formed metal-ligand complexes was established by slope analysis. Pb(II) ions were quantitatively extracted in the form of 2:1 Pb(II)-resorcin[4]arene complex from aqueous solutions of pH 5.5 to the solution of ligand in chloroform. Competitive solvent extraction experiments in the presence of Zn(II) and Cd(II) ions were also carried out and high selectivity of the extractant towards Pb(II) over Zn(II) and Cd(II) was found. The selectivity order was: Pb(II) >> Cd(II) > Zn(II).
Źródło:
Physicochemical Problems of Mineral Processing; 2013, 49, 1; 213-222
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Extraction of neodymium(III) from aqueous solutions by solvent extraction with Cyanex® 572
Autorzy:
Allahkarami, Ebrahim
Rezai, Bahram
Bozorgmehr, Mohsen
Adib, Saeed
Powiązania:
https://bibliotekanauki.pl/articles/1447143.pdf
Data publikacji:
2021
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
liquid-liquid extraction
neodymium(III)
cyanex 572
diluent
Opis:
The present research aims at studying the extractability of Nd(III) by Cyanex® 572 as a new extractant form from nitrate solutions. The effects of contact time, the concentration of nitrate ion, hydrogen ion, and extractant, and type of diluent were discussed, suggesting that the extraction of neodymium with Cyanex 572 was found to be a cation-exchange mechanism releasing three $H^+$ ion during the extraction. Cation- exchange mechanism of Nd(III) with Cyanex 572 was studied using slope analysis. Hydrogen ion concentration strongly influences the extraction behavior of Nd(III) in the solvent extraction. Results showed that three moles of Cyanex 572 are incorporated in the extraction process of one-mole neodymium(III) from the aqueous solutions. The concentration of nitrate ion in the aqueous solution has positive effect on the extraction efficiency of neodymium due to the salting out effect. The type of diluent influences the extraction efficiency of Nd(III). Results indicated that non-polar diluents were suitable solvents for the extraction of neodymium(III).
Źródło:
Physicochemical Problems of Mineral Processing; 2021, 57, 3; 127-135
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Solvent extraction behaviour of scandium from lateritic nickel-cobalt ores using different organic reagents
Autorzy:
Ferizoglu, E.
Kaya, S.
Topkaya, Y. A.
Powiązania:
https://bibliotekanauki.pl/articles/110877.pdf
Data publikacji:
2018
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
Solvent extraction
laterites
scandium
mixed hydroxide precipitate
Opis:
Scandium is one of the most important and strategic metals that can be recovered as a by-product from lateritic nickel-cobalt ores. In this research, different extractants were investigated to extract scandium from sulphate medium by using solvent extraction method. Generally, the organic extractants are classified as acidic, neutral and basic reagents. Thus, the aim of the present study was to compare scandium extraction efficiencies of some acidic, neutral and basic organic reagents. For this reason, Ionquest 290 (Bis(2,4,4-trimethylpenthyl) phosphonic acid), DEHPA (Di(2-ethylhexyl) phosphoric acid), Cyanex 272 ((Bis(2,4,4-trimethylpentyl) phosphinic acid) which are acidic organophosphorus compounds, Cyanex 923 (Trialkyl phosphine oxide), which is a neutral organophosphorus compound, and Primene JMT, a basic extractant, were used. The extraction efficiencies of these extractants were studied with respect to the extractant concentration at the same pH and O/A (organic/aqueous) phase ratio. As a result of this study, DEHPA and Primene JMT were found to have high scandium extraction efficiencies with lower impurity co-extractions at pH=0.55 with O/A phase ratio 1/1.
Źródło:
Physicochemical Problems of Mineral Processing; 2018, 54, 2; 538-545
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Separation of palladium(II) from mixtures of non-ferrous metal ions by solvent extraction
Autorzy:
Radzyminska-Lenarcik, E.
Witt, K.
Powiązania:
https://bibliotekanauki.pl/articles/115497.pdf
Data publikacji:
2016
Wydawca:
Fundacja na Rzecz Młodych Naukowców
Tematy:
metal separation
cobalt(II)
nickel(II)
copper(II)
palladium(II)
solvent extraction
alkylimidazole
separacja metali
kobalt(II)
nikiel(II)
miedź(II)
pallad(II)
ekstrakcja rozpuszczalnikiem
alkiloimidazole
Opis:
The possibility of Pd(II) ions separation from mixtures of Co(II), Ni(II), Cu(II) and Pd(II) ions by solvent extraction was studied, using 1-hexyl-2methylimidazole in chloroform as the extractant. The initial concentration of each ion was 10 mM. The tests were carried out at a temperature of 25°C, at a constant strength of the aqueous solution of I = 0.5, as maintained by the KCl solution. It was demonstrated that differences in the stability and structure of their coordination sphere as well as solubility of complexes with the extractant could be used for separating the Co(II), Ni(II), Cu(II) and Pd(II) ions by solvent extraction. Pd(II), which forms flat-square complexes in the solutions, passes easily into the organic phase and is easier separated from the mixture of Co(II), Ni(II), Cu(II) ions, which form octahedral or tetrahedral complexes. Extraction percentages were calculated. For the respective metals, their values increase for increasing concentrations of the extractant in the aqueous phase. The extraction percentage decreases in the following order: Pd(II) > Cu(II) > Co(II) > Ni(II). In the case of the quaternary mixture, the highest extraction percentage for Pd(II) (70%) was obtained at a pH=7.33. Separation coefficients were also calculated. The highest separation coefficients were obtained for the system: Pd(II)/Ni(II), Pd(II)/Co(II); at a pH of 5.4 for an aqueous solution, their values are 13.3 and 7.7, respectively.
Źródło:
Challenges of Modern Technology; 2016, 7, 1; 17-22
2082-2863
2353-4419
Pojawia się w:
Challenges of Modern Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Recovery of HCL from chloride leach solution of spent HDS catalyst by solvent extraction
Autorzy:
Banda, R.
Nguyen, T.H.
Lee, M.S.
Powiązania:
https://bibliotekanauki.pl/articles/185588.pdf
Data publikacji:
2013
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
HCl
extraction
stripping
recovery
TEHA
wydobycie
Opis:
In the present work, amine based extractant and its mixture with cationic and solvating extractants were tested for the extraction of HCl from chloride solution containing Al(III). The chloride feed solution resulted from the leaching of spent HDS (hydro-desulfurization) catalysts. For this purpose, amine extractants, such as TOA (trioctyl amine), Alamine 336 (a mixture of tri-octyl/decyl amine), Alamine 308 (tri-isooctyl amine), and TEHA (tri 2-ethylhexyl amine) were used and the extraction and stripping behavior of HCl was compared. The extracted HCl was easily stripped from loaded TEHA phase, when compared with the other tested tertiary amine system. Solvent extraction reaction of HCl by TEHA was determined from the extraction data. Unlike TOA and Alamine 336, adding cationic extractant to TEHA had negligible effect on the extraction and stripping of HCl. In our experimental ranges, no Al was extracted by amines and pure HCl was recovered. MaCabe-Thiele diagrams for the extraction and stripping of HCl by TEHA were constructed.
Źródło:
Chemical and Process Engineering; 2013, 34, 1; 153-163
0208-6425
2300-1925
Pojawia się w:
Chemical and Process Engineering
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Selective solvent extraction of some heavy metal ions from aqueous solutions by octafunctionalized resorcin[4]arenes
Autorzy:
Kończyk, Joanna
Dlugosz, Jan
Powiązania:
https://bibliotekanauki.pl/articles/110830.pdf
Data publikacji:
2020
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
solvent extraction
lead
chromium
calixresorcinarene
metal removal
Opis:
This paper presents the results of the study on the extraction capacity of 1,8,15,22-tetra(1- heptyl)resorcin[4]arene and its octasubstituted derivatives containing thiophosphoryl, ester and amide groups in the presence of Pb(II), Zn(II), Cd(II) and Cr(III) in solvent extraction process. Effects of the structure and concentration of the resorcinarene extractant and the composition of the aqueous phase as well as its acidity on the efficiency and selectivity of removal of the examined metal ions from model aqueous solutions were determined. The 1:1 stoichiometry for complexes formed between Pb(II) and Cr(III) and the octasubstituted resorcin[4]arenes was determined by classical slope analysis and loading test.
Źródło:
Physicochemical Problems of Mineral Processing; 2020, 56, 2; 271-285
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Solvent Extraction of Metal Ions from Sulfate Solutions Obtained in Leaching of Spent Ni-MH Batteries
Autorzy:
Pośpiech, Beata
Gęga, Jerzy
Powiązania:
https://bibliotekanauki.pl/articles/27315799.pdf
Data publikacji:
2019
Wydawca:
STE GROUP
Tematy:
solvent extraction
rare earth metals
nickel metal hydride batteries
ekstrakcja rozpuszczalnikiem
metale ziem rzadkich
akumulatory niklowo-wodorkowe
Opis:
The nickel metal hydride batteries (Ni-MH) are used in many electronic equipment, like cell phones, computers, cameras as well as hybrid cars. Spent batteries can be a rich source of many metals, especially rare earth elements (REE), such as lanthanum (La), cerium (Ce), neodymium (Nd), praseodymium (Pr), samarium (Sm), gadolinium (Gd). Ni-MH batteries also contain iron (Fe) as well as non-ferrous metals, i.e. nickel (Ni), cobalt (Co), zinc (Zn), manganese (Mn), etc. Leaching of such waste with sulfuric acid solutions is one among many methods recovering of useful metals in hydrometallurgical processes. The main aim of this work was separation of metal ions from pregnant leach liquor (PLL) by solvent extraction using phosphorous compounds and ionic liquids (ILs). The initial pH of the aqueous solution was 0.1. Di (2-ethylhexyl) phosphoric acid (D2EHPA), bis (2,2,4-trimethylpentyl) phosphinic acid (Cyanex 272), and phosphoniumionic liquid - trihexyl (tetradecyl) phosphonium bis (2,4,4- trimethylpentyl) phosphinate (Cyphos IL 104) were used as the selective extractants. The initial concentration of the extractants in an organic phase was equal to 0.1 mol dm-3. The obtained results show that the highest extraction efficiency was obtained for Fe(III) and Zn(II) in extraction experiments with 0.1 M D2EHPA at pH of 0.1. Ni(II), Co(II) and REE remained in the aqueous solutions. In the next stage, REE were extracted with the mixture of 0.1 M Cyanex 272 and 0.1 M Cyphos IL 104 at pH equal to 3.8. Finally, Ni(II) and Co(II) ions were efficiently removed from the aqueous phase using 0.1 M solution of Cyphos IL 104 at pH around 5.4.
Źródło:
New Trends in Production Engineering; 2019, 2, 2; 214-221
2545-2843
Pojawia się w:
New Trends in Production Engineering
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
New trends in the reprocessing of spent nuclear fuel. Separation of minor actinides by solvent extraction
Autorzy:
Narbutt, Jerzy
Powiązania:
https://bibliotekanauki.pl/articles/764096.pdf
Data publikacji:
2016
Wydawca:
Uniwersytet Marii Curie-Skłodowskiej. Wydawnictwo Uniwersytetu Marii Curie-Skłodowskiej
Opis:
Recycling of actinides from spent nuclear fuel by their selective separation followed by transmutation in fast reactors will optimize the use of natural uranium resources and minimize the long-term hazard from high-level nuclear waste. This paper describes solvent extraction processes recently developed, aimed at the separation of americium from lanthanide fission products as well as from curium present in the waste. Depicted are novel poly-N-heterocyclic ligands used as selective extractants of actinide ions from nitric acid solutions or as actinide-selective hydrophilic stripping agents.
Źródło:
Annales Universitatis Mariae Curie-Skłodowska, sectio AA – Chemia; 2016, 71, 1
2083-358X
Pojawia się w:
Annales Universitatis Mariae Curie-Skłodowska, sectio AA – Chemia
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Electron beam irradiation of r-SANEX and i-SANEX solvent extraction systems : analysis of gaseous products
Autorzy:
Szreder, T.
Kocia, R.
Powiązania:
https://bibliotekanauki.pl/articles/148074.pdf
Data publikacji:
2015
Wydawca:
Instytut Chemii i Techniki Jądrowej
Tematy:
electron beam irradiation
radiolytic gaseous products
gas chromatography
SANEX extraction systems
Opis:
1-Octanol/kerosene mixtures and water contacted with organic solvents were used as model solutions for r-SANEX and i-SANEX extractions systems. Investigations aimed on a quantitative evaluation of gaseous products generated in these systems under exposure to an electron beam irradiation. Influence of O2, HNO3 and the presence of model ligands and complexes on the radiation chemical yields was studied. Relatively high G(H2) values (up to 420 nmol∙J-1) for the organic phase compromise the safety issues of the extraction process and should be considered on the stage of extraction apparatus design. Based on the obtained results gaseous hydrocarbons seem to have negligible impact on safety issue. The upper limit of G(H2) values in water contacted with organic phase was established to be 85 nmol∙J-1. This value is relatively low, however, the literature data indicate that G(H2) values measured in aqueous solutions are over twice higher for α-particles irradiation than for electron beam or γ-irradiation. Thus, further investigations of these systems are necessary.
Źródło:
Nukleonika; 2015, 60, No. 4, part 2; 899-905
0029-5922
1508-5791
Pojawia się w:
Nukleonika
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
TS-BTPhen as a promising hydrophilic complexing agent for selective Am(III) separation by solvent extraction
Autorzy:
Kaufholz, P.
Sadowski, F.
Wilden, A.
Modolo, G.
Lewis, F. W.
Smith, A. W.
Harwood, L. M.
Powiązania:
https://bibliotekanauki.pl/articles/147226.pdf
Data publikacji:
2015
Wydawca:
Instytut Chemii i Techniki Jądrowej
Tematy:
Am-Cm separation
TODGA
TS-BTPhen
liquid-liquid extraction
Opis:
The novel hydrophilic back-extraction agent TS-BTPhen (3,3',3'',3'''-[3-(1,10-phenanthroline-2,9- -diyl)-1,2,4-triazine-5,5,6,6-tetrayl]tetrabenzenesulfonic acid) was tested for its selectivity towards Am(III) over Cm(III) and Eu(III) with a TODGA (N,N,N',N'-tetraoctyldiglycolamide) based solvent. Batch experiments were carried out using TS-BTPhen dissolved in aqueous nitric acid solution with tracers of 152Eu, 241Am and 244Cm. A signifi cant increase of the separation factor for Cm over Am from SFCm/Am = 1.6 up to SFCm/Am = 3.3 was observed compared to the use of a TODGA-nitric acid system alone. Furthermore, stripping was possible at high nitric acid concentrations (0.6–0.7 mol/L) resulting in a low sensitivity to acidity changes. The infl uence of the TS-BTPhen concentration was analyzed. A slope of –2 was expected taking into account literature stoichiometries of the lipophilic analogue CyMe4BTPhen. However, a slope of –1 was found. Batch stripping kinetics showed fast kinetics for the trivalent actinides. As an alternative organic ligand the methylated TODGA derivate Me-TODGA (2-methyl-N,N,N',N'-tetraoctyldiglycolamide) was tested in combination with the hydrophilic TS-BTPhen. The Am(III) separation was achieved at even higher nitric acid concentrations compared to TODGA.
Źródło:
Nukleonika; 2015, 60, No. 4, part 2; 815-820
0029-5922
1508-5791
Pojawia się w:
Nukleonika
Dostawca treści:
Biblioteka Nauki
Artykuł

Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies