scholarly journals Determination of complex formation constants of neptunium(V) with propionate and lactate in 0.5–2.6 m NaCl solutions at 22–60°C using a solvent extraction technique

2019 ◽  
Vol 107 (7) ◽  
pp. 623-634
Author(s):  
Aleksandr N. Vasiliev ◽  
Nidhu L. Banik ◽  
Rémi Marsac ◽  
Stepan N. Kalmykov ◽  
Christian M. Marquardt

Abstract Natural clay rocks like Opalinus (OPA) and Callovo-Oxfordian (COx) clay rock are considered as potential host rocks for deep geological disposal of nuclear waste. However, small organic molecules such as propionate and lactate exist in clay rock pore water and might enhance Np mobility through a complexation process. Therefore, reliable complex formation data are required in the frame of the Safety Case for a nuclear waste repository. A solvent extraction technique was applied for the determination of ${\rm{NpO}}_2^ + $ complexation with propionate and lactate. Extraction was conducted from isoamyl alcohol solution containing 10−3 M TTA and 5 · 10−4 M 1,10-phenanthroline. Experiments were performed in 0.5–2.6 m NaCl solutions at temperatures ranging from 22 to 60 °C. Formation of 1:1 Np(V) complexes for propionate and lactate was found under the studied conditions. The SIT approach was applied to calculate equilibrium constants β°(T) at zero ionic strength from the experimental data. Log β°(T) is found linearly correlated to 1/T for propionate and lactate, evidencing that heat capacity change is near 0. Molal reaction enthalpy and entropy ( ${\Delta _{\rm{r}}}H_{\rm{m}}^ \circ $ and ${\Delta _{\rm{r}}}S_{\rm{m}}^ \circ $ ) could therefore be derived from the integrated van’t Hoff equation. Data for log β° (298.15 K) are in agreement with literature values for propionate and lactate. Np(V) speciation was calculated for concentrations of acetate, propionate and lactate measured in clay pore waters of COx. In addition, the two site protolysis non-electrostatic surface complexation and cation exchange (2SPNE SC/CE) model was applied to quantitatively describe the influence of Np(V) complexation on its uptake on Na-illite, a relevant clay mineral of OPA and COx.

2000 ◽  
Vol 88 (9-11) ◽  
Author(s):  
D.N. Kurk ◽  
Gregory R. Choppin

Complexation of Ni(II) and Co(II) by unfractionated humic acid (HA) was measured in 0.3 to 5.0 m NaCl solutions at pH 6 and 20 °C, using a solvent extraction technique. The dissociation constants and capacities of the humic acid were investigated in 0.1 to 5.0 m NaCl solutions at 25 °C using potentiometric titration methods.


2017 ◽  
Vol 9 (4) ◽  
pp. 110 ◽  
Author(s):  
Yoshihiro Kudo ◽  
Tomohiro Amano ◽  
Satoshi Ikeda

Extraction constants (Kex± & Kex) were determined at 298 K for the extraction of sodium picrate (NaPic) by nitrobenzene (NB), 1,2-dichloroethane (DCE) and dichloromethane using 3m-crown-m ethers and their benzo-derivatives (m = 5, 6; abbreviated as L) together with the determination of conditional distribution constants (KD,Pic) of picrate ion, Pic-, into these diluents. The K1,org (= [NaLPic]org/[NaL+]org[Pic-]org) values at the organic (org) phases, such as NB & DCE, were calculated from the relation Kex/Kex± = K1,org. Distribution equilibrium-potential differences (Dfeq) at extraction equilibria were evaluated from the equation Dfeq = -0.05916´(log KD,Pic - constant) at 298 K. Correlations of the above equilibrium constants, particularly Kex±, with Dfeq were examined. Furthermore, the standard formal potentials for Na+ transfers across the interfaces were briefly evaluated from calculated Dfeq, [Na+] and [Pic-]org. The above extraction systems were characterized by K1,org and the complex formation constants of Na+ with L in the org phases.


2006 ◽  
Vol 94 (8) ◽  
Author(s):  
Sofie Andersson ◽  
Klaus Eberhardt ◽  
Christian Ekberg ◽  
Jan-Olov Liljenzin ◽  
Mikael Nilsson ◽  
...  

SummaryFor lanthanides and actinides, nitrate complex formation is an important factor with respect to the reprocessing of nuclear fuels and in studies that treat partitioning and transmutation/conditioning. Different techniques, including microcalorimetry, various kinds of spectroscopy, ion-exchange and solvent extraction, can be used to determine stability constants of nitrate complex formation. However, it is uncommon that all lanthanides are studied at the same time, using the same experimental conditions and technique. The strengths of the complexes are different for lanthanides and actinides, a feature that may assist in the separation of the two groups. This paper deals with nitrate complex formation of lanthanides using a solvent extraction technique. Trace amounts of radioactive isotopes of lanthanides were produced at the TRIGA Mainz research reactor and at the Institutt for Energiteknikk in Kjeller, Norway (JEEP II reactor).The extraction of lanthanide ions into an organic phase consisting of 2,6-bis-(benzoxazolyl)-4-dodecyloxylpyridine, 2-bromodecanoic acid andExtraction curves for La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Dy, Ho and Er were obtained and stability constants for their nitrate complex formation were estimated. Tb, Tm, Yb and Lu were also investigated, but no stability constants could be determined. The distribution ratios for the metal ions at low nitrate ion concentration were obtained at the same time, showing the effect of lanthanide contraction resulting in decreasing extraction along the series. A clear tetrad effect in the lanthanide group was also found.


Sign in / Sign up

Export Citation Format

Share Document