Molekulardynamische und quantenchemische Rechnungen an wässrigen Actinidkomplexen

Aus molekulardynamischen und quantenchemischen Rechnungen an wässrigen Actinidkomplexen werden strukturelle, spektroskopische und thermodynamische Daten errechnet. Diese zeigen eine sehr gute Übereinstimmung mit aktuellen experimentell gewonnenen Daten und können daher in weiteren Studien zur Vorhersage oder Erklärung von Messwerten genutzt werden. Die gewonnen Ergebnisse gehen unter anderem als Parameter in Langzeitstudien zur Endlagersicherheit ein

Structure and separation quality of various N- and O-donor ligands from quantum-chemical calculations

Although BTP (2,6-di(1,2,4-triazin-3-yl)pyridine) has been proven to be a highly effective N-donor ligand for the selective An(III)/Ln(III) separation, the origin of its selectivity is still under discussion. We present in this paper quantum-chemical calculations at the density functional theory (DFT) and MP2 level which highlight the role of the aquo ions in the separation process. Furthermore these data will be the reference for future force-field development to investigate the differences in An(III) complexation reactions compared to their Ln(III) counterparts

Stoichiometry of An(III)–DMDOHEMA complexes formed during solvent extraction

N,N’-Dimethyl,N,N’-dioctylhexylethoxymalonamide (DMDOHEMA) is used to separate An(III) and Ln(III) from fission products in several liquid–liquid extraction processes that aim at recycling actinides. The stoichiometry of the extracted complexes is important for a complete understanding of the processes. The presented work focuses on the complexation of Cm(III) with DMDOHEMA studied by TRLFS in mono- and biphasic (solvent extraction) systems. The formation of [Cm(DMDOHEMA)n]3+ (n = 1–3) in 1-octanol containing 1.7 mol L−1 of water with log β’1 = 2.6 ± 0.3, log β’2 = 4.0 ± 0.5, log β’3 = 4.3 ± 0.5 was confirmed. In addition, fluorescence lifetime measurements indicated the formation of a 1 : 4 complex. Furthermore, solvent extraction experiments were performed, varying the proton and nitrate concentrations. TRLFS measurements of organic phases confirmed the existence of two species, [Cm(DMDOHEMA)3(NO3) (H2O)1–2]2+ (dominant at high proton and nitrate concentrations) and [Cm(DMDOHEMA)4(H2O)]3+ (dominant at low proton and nitrate concentrations). To support the proposed stoichiometries, vibronic sideband spectroscopy (VSBS) was employed, allowing the observation of vibrations of functional groups coordinated to the probed metal ion. Clear differences between the vibronic side bands of the 1 : 3 and 1 : 4 complex in the range of 900–1300 cm−1 were observed. Vibrational spectra calculated by DFT complimented the experimental data and confirmed the proposed stoichiometries. They revealed a monodentate coordination mode of the nitrate and two water molecules in the 1 : 3 complex

Radiation dose and image quality of high-pitch emergency abdominal CT in obese patients using third-generation dual-source CT (DSCT)

In this third-generation dual-source CT (DSCT) study, we retrospectively investigated radiation dose and image quality of portal-venous high-pitch emergency CT in 60 patients (28 female, mean age 56 years) with a body mass index (BMI) (3) 30 kg/m(2). Patients were dichotomized in groups A (median BMI 31.5 kg/m(2);n = 33) and B (36.8 kg/m(2);n = 27). Volumetric CT dose index (CTDIvol), size-specific dose estimate (SSDE), dose length product (DLP) and effective dose (ED) were assessed. Contrast-to-noise ratio (CNR) and dose-independent figure-of-merit (FOM) CNR were calculated. Subjective image quality was assessed using a five-point scale. Mean values of CTDIvol, SSDE as well as normalized DLP and ED were 7.6 +/- 1.8 mGy, 8.0 +/- 1.8 mGy, 304 +/- 74 mGy * cm and 5.2 +/- 1.3 mSv for group A, and 12.6 +/- 3.7 mGy, 11.0 +/- 2.6 mGy, 521 +/- 157 mGy * cm and 8.9 +/- 2.7 mSv for group B (p 36.8 kg/m(2)

Opportunities and challenges of applying advanced X-ray spectroscopy to actinide and lanthanide N-donor ligand systems

N-donor ligands such as n-Pr-BTP [2,6-bis­(5,6-di­propyl-1,2,4-triazin-3-yl)­pyridine] preferentially bind trivalent actinides (An$^{3+}$) over trivalent lanthanides (Ln$^{3+}$) in liquid–liquid separation. However, the chemical and physical processes responsible for this selectivity are not yet well understood. Here, an explorative comparative X-ray spectroscopy and computational (L3-edge) study for the An/Ln L$_{3}$-edge and the N K-edge of [An/Ln(n-Pr-BTP) $_{3}$](NO$_{3}$)$_{3}$, [Ln(n-Pr-BTP) $_{3}$](CF$_{3}$SO$_{3}$)$_{3}$ and [Ln(n-Pr-BTP) $_{3}$](ClO$_{4}$)$_{3}$ complexes is presented. High-resolution X-ray absorption near-edge structure (HR-XANES) L$_{3}$-edge data reveal additional features in the pre- and post-edge range of the spectra that are investigated using the quantum chemical codes FEFF and FDMNES. X-ray Raman spectroscopy studies demonstrate the applicability of this novel technique for investigations of liquid samples of partitioning systems at the N K-edge

Pu(III) and Cm(III) in the presence of EDTA: aqueous speciation, redox behavior, and the impact of Ca(II)

The impact of calcium on the solubility, redox behavior, and speciation of the An(iii)–EDTA (An = Pu or Cm) system under reducing, anoxic conditions was investigated through batch solubility experiments, X-ray absorption spectroscopy (XAS), density functional theory (DFT), and time-resolved laser fluorescence spectroscopy (TRLFS). Batch solubility experiments were conducted from undersaturation using Pu(OH)(3)(am) as the solid phase in contact with 0.1 M NaCl–NaOH–HCl–EDTA–CaCl(2) solutions at [EDTA] = 1 mM, pH(m) = 7.5–9.5, and [CaCl(2)] ≤20 mM. Additional samples targeted brine systems represented by 3.5 M CaCl(2) and WIPP simulated brine. Solubility data in the absence of calcium were well-described by Pu(iii)–EDTA thermodynamic models, thus supporting the stabilization of Pu(iii)–EDTA complexes in solution. Cm(iii)–EDTA TRLFS data suggested the stepwise hydrolysis of An(iii)-EDTA complexes with increasing pH, and current Pu(iii)-EDTA solubility models were reassessed to evaluate the possibility of including Pu(iii)–OH–EDTA complexes and to calculate preliminary formation constants. Solubility data in the presence of calcium exhibited nearly constant log m(Pu)(tot), as limited by total ligand concentration, with increasing [CaCl(2)](tot), which supports the formation of calcium-stabilized Pu(iii)–EDTA complexes in solution. XAS spectra without calcium showed partial oxidation of Pu(iii) to Pu(iv) in the aqueous phase, while calcium-containing experiments exhibited only Pu(iii), suggesting that Ca–Pu(iii)–EDTA complexes may stabilize Pu(iii) over short timeframes (t ≤45 days). DFT calculations on the Ca–Pu(iii)–EDTA system and TRLFS studies on the analogous Ca–Cm(iii)–EDTA system show that calcium likely stabilizes An(iii)–EDTA complexes but can also potentially stabilize An(iii)–OH–EDTA species in solution. This hints towards the possible existence of four major complex types within Ca–An(iii)–EDTA systems: An(iii)–EDTA, An(iii)–OH–EDTA, Ca–An(iii)–EDTA, and Ca–An(iii)–OH–EDTA. While the exact stoichiometry and degree of ligand protonation within these complexes remain undefined, their formation must be accounted for to properly assess the fate and transport of plutonium under conditions relevant to nuclear waste disposal

Complexation of lanthanides, actinides and transition metal cations with a 6-(1,2,4-triazin-3-yl)-2,2’:6’,2’’-terpyridine ligand: implications for actinide(III) /lanthanide(III) partitioning

The quadridentate N-heterocyclic ligand 6-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-1,2,4-benzotriazin-3-yl)-2,2’:6’,2’’-terpyridine (CyMe4-hemi-BTBP) has been synthesized and its interactions with Am(III), U(VI), Ln(III) and some transition metal cations have been evaluated by X-ray crystallographic analysis, Am(III)/Eu(III) solvent extraction experiments, UV absorption spectrophotometry, NMR studies and ESI-MS. Structures of the 1:1 complexes with Eu(III), Ce(III) and the linear uranyl (UO22+) ion were obtained by X-ray crystallographic analysis, and showed similar coordination behavior to related BTBP complexes. In methanol, the stability constants of the Ln(III) complexes are slightly lower than those of the analogous quadridentate bis-triazine BTBP ligands, while the stability constant for the Yb(III) complex is higher. 1H NMR titrations and ESI-MS with lanthanide nitrates showed that the ligand forms only 1:1 complexes with Eu(III), Ce(III) and Yb(III), while both 1:1 and 1:2 complexes were formed with La(III) and Y(III) in acetonitrile. A mixture of isomeric chiral 2:2 helical complexes was formed with Cu(I), with a slight preference (1.4:1) for a single directional isomer. In contrast, a 1:1 complex was observed with the larger Ag(I) ion. The ligand was unable to extract Am(III) or Eu(III) from nitric acid solutions into 1-octanol, except in the presence of a synergist at low acidity. The results show that the presence of two outer 1,2,4-triazine rings is required for the efficient extraction and separation of An(III) from Ln(III) by quadridentate N-donor ligand

Highly efficient separation of actinides from lanthanides by a phenanthroline-derived bis-triazine ligand

The synthesis, lanthanide complexation, and solvent ex- traction of actinide(III) and lanthanide(III) radiotracers from nitric acid solutions by a phenanthroline-derived quadridentate bis-triazine ligand are described. The ligand separates Am(III) and Cm(III) from the lanthanides with remarkably high efficiency, high selectivity, and fast extraction kinetics compared to its 2,2'-bipyridine counterpart. Structures of the 1:2 bis-complexes of the ligand with Eu(III) and Yb(III) were elucidated by X-ray crystallography and force field calculations, respec-tively. The Eu(III) bis-complex is the first 1:2 bis-complex of a quadridentate bis-triazine ligand to be characterized by crystallography. The faster rates of extraction were verified by kinetics measurements using the rotating membrane cell technique in several diluents. The improved kinetics of metal ion extraction are related to the higher surface activity of the ligand at the phase interface. The improvement in the ligand's properties on replacing the bipyridine unit with a phenanthroline unit far exceeds what was anticipated based on ligand design alone