Coprecipitation Experiments Using Simulated Spent Fuel Solutions in the Presence of Metallic Iron in Synthetic Bentonitic-Granitic Water Under Oxidising Conditions

2004 ◽  
Vol 824 ◽  
Author(s):  
Javier Quiñones ◽  
Ángel González de la Huebra ◽  
Aurora Martínez Esparza
Keyword(s):  
Metallic Iron ◽  
Room Temperature ◽  
Uranium Concentration ◽  
Solid Phase ◽  
Spent Fuel ◽  
Secondary Phases ◽  
Bulk Solid ◽  
Show Evidence ◽  
Ph Range ◽  
Iron Material

AbstractThis paper presents the results obtained from coprecipitation experiments of uranyl solutions in the presence of metallic iron and/or its alteration phases in synthetic bentonitic-granitic composition water. Experiments were done under oxidising conditions at room temperature. The pH range covered was 7.4 – 8.8. Changes in the uranium concentrations and the characterisation of the secondary phases formed in the experiments were done using XRD and SEM-EDS and are presented herein.Final uranium concentration values were in the range of 2·10−5 – 5·10−4 mol (kg of H2O)−1. In all cases, results from these experiments did not show evidence of a clear effect due to the presence of iron (metallic or previously corroded) on the uranium concentration. These data were similar to those obtained by coprecipitation in similar conditions but in absence of iron material. Boltwoodite was observed [K2(UO2)2(SiO3)2(OH)2·3H2O] in iron surface materials and characterized in all experiments. Based on the experimental data obtained (uranium concentration in solution and bulk solid phase characterisation) we propose the following surface-mediated reaction:2 K+ + 2 H4SiO4 + 2 UO2+2 + 3 H2O ⇔ K2(UO2)2(SiO3)2(OH)2·3H2O + 6 H+

Coprecipitation Studies from Simfuel Solutions in 5 m NaCl Media

1996 ◽  
Vol 465 ◽  
Author(s):  
P. Diaz-Arocas ◽  
J. Garcia-Serrano
Keyword(s):  
Fission Products ◽  
Solution Concentration ◽  
Laser Fluorescence ◽  
Spent Fuel ◽  
Secondary Phases ◽  
Minor Elements ◽  
Icp Ms ◽  
Upper Limits ◽  
Ph Range ◽  
Irradiated Fuel

ABSTRACTExtensive Research is performed in many countries in order to evaluate the spent fuel behaviour under repository conditions. Several aspects as the control of the oxidative spent fuel dissolution by secondary phases formation are not yet clear.Coprecipitation experiments from SIMFUEL solutions are performed to study if minor elements will influence the formation of secondary phases. Therefore, coprecipitation studies from SIMFUEL solutions aims at identification of stable phases of significant simulated fission products. These experiments provide upper limits for solution concentration and distribution ratios of simulate fission products at several pH values. SIMFUEL pellets, which simulate an irradiated fuel with burnup of 50 GWd/tU were provided by AECL Research Laboratories, Canada. Experiments were carried out by addition of an aliquot of the initial SIMFUEL solution to 5 m NaCI free of carbonates solution. The selected pH was maintained constant during the experiments. The pH range considered was from 5.5 to 9.3. Analyses of the solutions were performed for uranium by Laser fluorescence and for the minor elements by ICP-MS. Solid phases formed at pH 5.5 were dissolved and analysed by ICP-MS. Results of the evolution in solution vs. pH of simulated fission products concentrations are shown in this paper.

Effect of temperature on the solubility and solid phase stability of zirconium hydroxide

2013 ◽  
Vol 101 (10) ◽  
pp. 645-651 ◽  
Author(s):  
T. Kobayashi ◽  
D. Bach ◽  
M. Altmaier ◽  
T. Sasaki ◽  
H. Moriyama
Keyword(s):  
Phase Stability ◽  
Room Temperature ◽  
Solubility Product ◽  
Elevated Temperatures ◽  
Solid Phase ◽  
Zirconium Hydroxide ◽  
Effect Of Temperature ◽  
Crystalline Oxide ◽  
Ph Range ◽  
Colloidal Species

Summary The solubility and solid phase stability of zirconium hydroxide was investigated in the acidic pH range after heating the aqueous samples at 50, 70 and 90 ◦C. The solubility measured at room temperature after exposing the batch samples to elevated temperatures for a given period of time significantly decreased with increasing heating periods. The Zr concentrations at given pH after heating at 90 ◦C for 3 weeks are about 5 orders of magnitude lower than the solubility of amorphous zirconium hydroxide (Zr(OH)4(am)) kept at room temperature. Size distributions of the Zr colloidal species after heating were investigated by sequential filtration using different pore-sized membranes, and the contribution of the colloidal species to the solubility was assessed. The TEM images and XRD spectra of the solid phases after heating indicated the agglomeration and crystallization of the initial amorphous hydroxide solid phase. The solid phase was identified as crystalline oxide after heating at 90◦C. The solubility product determined from the solubility data excluding contributions of colloidal species is correlated to the particle size of the solid phase.

Photoluminescence and Magnetic Properties of Undoped and (Mn, Co) co-doped ZnO Nanoparticles

2020 ◽  
Vol 16 (4) ◽  
pp. 655-666
Author(s):  
Mona Rekaby
Keyword(s):  
Magnetic Properties ◽  
Zno Nanoparticles ◽  
Room Temperature ◽  
Magnetic Measurements ◽  
Structural Defects ◽  
Ferromagnetic Behavior ◽  
Secondary Phases ◽  
Antiferromagnetic Ordering ◽  
Doped Zno ◽  
Co Doped

Objective: The influence of Manganese (Mn2+) and Cobalt (Co2+) ions doping on the optical and magnetic properties of ZnO nanoparticles was studied. Methods: Nanoparticle samples of type ZnO, Zn0.97Mn0.03O, Zn0.96Mn0.03Co0.01O, Zn0.95Mn0.03 Co0.02O, Zn0.93Mn0.03Co0.04O, and Zn0.91Mn0.03Co0.06O were synthesized using the wet chemical coprecipitation method. Results: X-ray powder diffraction (XRD) patterns revealed that the prepared samples exhibited a single phase of hexagonal wurtzite structure without any existence of secondary phases. Transmission electron microscope (TEM) images clarified that Co doping at high concentrations has the ability to alter the morphologies of the samples from spherical shaped nanoparticles (NPS) to nanorods (NRs) shaped particles. The different vibrational modes of the prepared samples were analyzed through Fourier transform infrared (FTIR) measurements. The optical characteristics and structural defects of the samples were studied through Photoluminescence (PL) spectroscopy. PL results clarified that Mn2+ and Co2+ doping quenched the recombination of electron-hole pairs and enhanced the number of point defects relative to the undoped ZnO sample. Magnetic measurements were carried out at room temperature using a vibrating sample magnetometer (VSM). (Mn, Co) co-doped ZnO samples exhibited a ferromagnetic behavior coupled with paramagnetic and weak diamagnetic contributions. Conclusion: Mn2+ and Co2+ doping enhanced the room temperature Ferromagnetic (RTFM) behavior of ZnO. In addition, the signature for antiferromagnetic ordering between the Co ions was revealed. Moreover, a strong correlation between the magnetic and optical behavior of the (Mn, Co) co-doped ZnO was analyzed.

scholarly journals 68Ga, 44Sc and 177Lu-labeled AAZTA5-PSMA-617: synthesis, radiolabeling, stability and cell binding compared to DOTA-PSMA-617 analogues

2020 ◽  
Vol 5 (1) ◽  
Author(s):  
Jean-Philippe Sinnes ◽  
Ulrike Bauder-Wüst ◽  
Martin Schäfer ◽  
Euy Sung Moon ◽  
Klaus Kopka ◽  
...  
Keyword(s):  
Human Serum ◽  
Room Temperature ◽  
Solid Phase ◽  
Negative Influence ◽  
Binding Motif ◽  
Lncap Cells ◽  
Cell Binding ◽  
Binding Characteristics

Abstract Background The AAZTA chelator and in particular its bifunctional derivative AAZTA5 was recently investigated to demonstrate unique capabilities to complex diagnostic and therapeutic trivalent radiometals under mild conditions. This study presents a comparison of 68Ga, 44Sc and 177Lu-labeled AAZTA5-PSMA-617 with DOTA-PSMA-617 analogues. We evaluated the radiolabeling characteristics, in vitro stability of the radiolabeled compounds and evaluated their binding affinity and internalization behavior on LNCaP tumor cells in direct comparison to the radiolabeled DOTA-conjugated PSMA-617 analogs. Results AAZTA5 was synthesized in a five-step synthesis and coupled to the PSMA-617 backbone on solid phase. Radiochemical evaluation of AAZTA5-PSMA-617 with 68Ga, 44Sc and 177Lu achieved quantitative radiolabeling of > 99% after less than 5 min at room temperature. Stabilities against human serum, PBS buffer and EDTA and DTPA solutions were analyzed. While there was a small degradation of the 68Ga complex over 2 h in human serum, PBS and EDTA/DTPA, the 44Sc and 177Lu complexes were stable at 2 h and remained stable over 8 h and 1 day. For all three compounds, i.e. [natGa]Ga-AAZTA5-PSMA-617, [natSc]Sc-AAZTA5-PSMA-617 and [natLu]Lu-AAZTA5-PSMA-617, in vitro studies on PSMA-positive LNCaP cells were performed in direct comparison to radiolabeled DOTA-PSMA-617 yielding the corresponding inhibition constants (Ki). Ki values were in the range of 8–31 nM values which correspond with those of [natGa]Ga-DOTA-PSMA-617, [natSc]Sc-DOTA-PSMA-617 and [natLu]Lu-DOTA-PSMA-617, i.e. 5–7 nM, respectively. Internalization studies demonstrated cellular membrane to internalization ratios for the radiolabeled 68Ga, 44Sc and 177Lu-AAZTA5-PSMA-617 tracers (13–20%IA/106 cells) in the same range as the ones of the three radiolabeled DOTA-PSMA-617 tracers (17–20%IA/106 cells) in the same assay. Conclusions The AAZTA5-PSMA-617 structure proved fast and quantitative radiolabeling with all three radiometal complexes at room temperature, excellent stability with 44Sc, very high stability with 177Lu and medium stability with 68Ga in human serum, PBS and EDTA/DTPA solutions. All three AAZTA5-PSMA-617 tracers showed binding affinities and internalization ratios in LNCaP cells comparable with that of radiolabeled DOTA-PSMA-617 analogues. Therefore, the exchange of the chelator DOTA with AAZTA5 within the PSMA-617 binding motif has no negative influence on in vitro LNCaP cell binding characteristics. In combination with the faster and milder radiolabeling features, AAZTA5-PSMA-617 thus demonstrates promising potential for in vivo application for theranostics of prostate cancer.

scholarly journals Non-Destructive Detection of Pentachlorophenol Residues in Historical Wooden Objects

Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1052
Author(s):  
Ida Kraševec ◽  
Nataša Nemeček ◽  
Maja Lozar Štamcar ◽  
Irena Kralj Cigić ◽  
Helena Prosen
Keyword(s):  
Indoor Air ◽  
Room Temperature ◽  
Quantitative Methods ◽  
Solid Phase ◽  
Contact Mode ◽  
Solvent Extraction Method ◽  
Museum Objects ◽  
Wooden Furniture ◽  
Non Destructive ◽  
Heritage Collections

Wood is a natural polymeric material that is an important constituent of many heritage collections. Because of its susceptibility to biodegradation, it is often chemically treated with substances that can be harmful to human health. One of the most widely used wood preservatives was pentachlorophenol (PCP), which is still present in museum objects today, although its use has been restricted for about forty years. The development of non-destructive methods for its determination, suitable for the analysis of valuable objects, is therefore of great importance. In this work, two non-destructive solid-phase microextraction (SPME) methods were developed and optimized, using either headspace or contact mode. They were compared with a destructive solvent extraction method and found to be suitable for quantification in the range of 7.5 to 75 mg PCP/kg wood at room temperature. The developed semi-quantitative methods were applied in the wooden furniture depot of National Museum of Slovenia. PCP was detected inside two furniture objects using headspace mode. The pesticide lindane was also detected in one object. The indoor air of the depot with furniture was also sampled with HS SPME, and traces of PCP were found. According to the results, SPME methods are suitable for the detection of PCP residues in museum objects and in the environment.

Room temperature rectification in tapered-channel thermal diodes through nanoscale confinement-induced liquid–solid phase change

2021 ◽  
Vol 129 (7) ◽  
pp. 075103
Author(s):  
Matt Jacobs ◽  
Xinran Zhou ◽  
Edgar Olivera ◽  
Ryan Sheil ◽  
Shu Huang ◽  
...  
Keyword(s):  
Phase Change ◽  
Room Temperature ◽  
Solid Phase ◽  
Tapered Channel

scholarly journals The effect of short-term storage temperature on the key headspace volatile compounds observed in Canadian faba bean flour

2021 ◽  
pp. 108201322199884
Author(s):  
Rami Akkad ◽  
Ereddad Kharraz ◽  
Jay Han ◽  
James D House ◽  
Jonathan M Curtis
Keyword(s):  
Fatty Acids ◽  
Volatile Compounds ◽  
Room Temperature ◽  
Unsaturated Fatty Acids ◽  
Solid Phase ◽  
Short Term ◽  
Bean Flour ◽  
Odour Activity Value ◽  
Short Term Storage ◽  
Term Storage

The odour emitted from the high-tannin fab bean flour ( Vicia faba var. minor), was characterized by headspace solid-phase microextraction/gas chromatography-mass spectrometry (HS-SPME/GC–MS). The relative odour activity value (ROAV) was used to monitor the changes in key volatile compounds in the flour during short-term storage at different temperature conditions. The key flavour compounds of freshly milled flour included hexanal, octanal, nonanal, decanal, 3-methylbutanal, phenyl acetaldehyde, (E)-2-nonenal, 1-hexanol, phenyl ethyl alcohol, 1-octen-3-ol, β-linalool, acetic acid, octanoic acid, and 3-methylbutyric acid; these are oxidative degradation products of unsaturated fatty acids and amino acids. Despite the low lipid content of faba beans, the abundances of aldehydes arising during room temperature storage greatly contributed to the flavour of the flour due to their very low odour thresholds. Two of the key volatiles responsible for beany flavour in flour (hexanal, nonanal) increased greatly after 2 weeks of storage at room temperature or under refrigerated conditions. These volatile oxidation products may arise as a result of enzymatic activity on unsaturated fatty acids, and was seen to be arrested by freezing the flour.

scholarly journals Biogeochemical Controls on the Potential for Long-Term Contaminant Leaching from Soils Developing on Historic Coal Mine Spoil

Soil Systems ◽  
2020 ◽  
Vol 5 (1) ◽  
pp. 3
Author(s):  
David Singer ◽  
Elizabeth Herndon ◽  
Laura Zemanek ◽  
Kortney Cole ◽  
Tyler Sanda ◽  
...  
Keyword(s):  
Coal Mine ◽  
Solid Phase ◽  
Microbial Community Composition ◽  
Toxic Metal ◽  
Soil Formation ◽  
Mineral Weathering ◽  
Mine Spoil ◽  
Secondary Phases ◽  
Undisturbed Soil

Coal mine spoil is widespread in US coal mining regions, and the potential long-term leaching of toxic metal(loid)s is a significant and underappreciated issue. This study aimed to determine the flux of contaminants from historic mine coal spoil at a field site located in Appalachian Ohio (USA) and link pore water composition and solid-phase composition to the weathering reaction stages within the soils. The overall mineralogical and microbial community composition indicates that despite very different soil formation pathways, soils developing on historic coal mine spoil and an undisturbed soil are currently dominated by similar mineral weathering reactions. Both soils contained pyrite coated with clays and secondary oxide minerals. However, mine spoil soil contained abundant residual coal, with abundant Fe- and Mn- (oxy)hydroxides. These secondary phases likely control and mitigate trace metal (Cu, Ni, and Zn) transport from the soils. While Mn was highly mobile in Mn-enriched soils, Fe and Al mobility may be more controlled by dissolved organic carbon dynamics than mineral abundance. There is also likely an underappreciated risk of Mn transport from coal mine spoil, and that mine spoil soils could become a major source of metals if local biogeochemical conditions change.

Effects of Aging on the Solubility of Palladium

1995 ◽  
Vol 412 ◽  
Author(s):  
C. Oda ◽  
H. Yoshikawa ◽  
M. Yui
Keyword(s):  
Aqueous Solution ◽  
Aging Time ◽  
Room Temperature ◽  
High Level Waste ◽  
Anaerobic Conditions ◽  
Dilute Aqueous Solution ◽  
Waste Repository ◽  
Ph Range ◽  
Effects Of Aging ◽  
High Level

AbstractPalladium solubility was measured in a dilute aqueous solution at room temperature in the pH range from 3 to 13 under anaerobic conditions. Crystalline Pd metal was clearly visible and the concentration of palladium in solution decreased gradually with aging time. The palladium concentrations in solution were less than 9.4×10-10M in the pH range from 4 to 10 and increased to 10-7M in the pH range greater than 10. This study suggests that palladium concentrations in certain high-level waste repository environments may be limited by Pd metal and may be less than 10-9M.

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