A new uranyl containing metal–organic framework, RPL-1 : [(UO2)2(C28H18O8)] . H2O (RPL for Radiochemical Processing Laboratory), was prepared, structurally characterized, and the solid-state photoluminescence properties explored. Single crystal X-ray diffraction data reveals the structure of RPL - 1 consists of two crystallographically unique three dimensional, interpenetrating nets with a 4,3-connected tbo topology. Each net contains large pores with an average width of 22.8 Å and is formed from monomeric, hexagonal bipyramidal uranyl nodes that are linked via 1,2,4,5-tetrakis(4-carboxyphenyl)benzene (TCPB) ligands. The thermal and photophysical properties of RPL-1 were investigated using thermogravimetric analysis and absorbance, fluorescence, and lifetime spectroscopies. The material displays excellent thermal stability and temperature dependent uranyl and TCPB luminescence. The framework is stable in aqueous media and due to the large void space (constituting 76 % of the unit cell by volume) can sequester organic dyes, the uptake of which induces a visible change to the color of the material. 相似文献
Seven 271Ds decay chains were identified in the bombardment of 208Pb targets with 311.5 and 314.3 MeV 64Ni projectiles using the Berkeley Gas-filled Separator. These data, combined with previous results, provide an excitation function for this reaction. From these results, an optimum energy of 321 MeV was estimated for the production of (272)111 in the new reaction 208Pb(65Cu,n). One decay chain was observed, resulting in a cross section of 1.7(+3.9)(-1.4) pb. This experiment confirms the discovery of element 111 by the Darmstadt Group who used the 209Bi(64Ni,n)(272)111 reaction. 相似文献
We are developing a medium-resolution autonomous in situ gamma detection system for marine and coastal waters. The system is designed to extract and preconcentrate isotopes of interest from natural waters prior to detection in order to eliminate signal attenuation of the gamma rays traveling through water and lower the overall background from the presence of naturally occurring radioactive isotopes (40K and U–Th series radionuclides). Filtration is used to preconcentrate target isotopes residing on suspended particles, while chemosorption is employed to preferentially extract truly dissolved components from the water column. Used filter and chemosorbent media will be counted autonomously using two LaBr3 detectors in a near 4-π configuration around the samples. A compact digital pulse processing system, developed in-house and capable of running in coincidence mode, is used to process the signal from the detectors to a small on-board computer. The entire system is extremely compact (9″ dia. × 30″ len.) and platform independent, but designed for initial deployment on a research buoy. A variety of commercial and in-house nano-porous chemosorbents have been selected, procured or produced, and these and filter and detector components have been tested. 相似文献
The Nuclear Forensics International Technical Working Group (ITWG), a community of nuclear forensic practitioners who respond to incidents involving nuclear and other radioactive material out of regulatory control, completed its fifth Collaborative Materials Exercise in 2017 (CMX-5). Forensic laboratories from 19 countries and one multinational organization aimed to advance nuclear forensic science and improve international cooperation in the event of a nuclear material security incident. In all, over 30 analytical techniques were utilized to investigate the samples, many techniques applying novel methods or offering improvements in turnaround time. An objective review of the state of practice and emerging application of analytical techniques of nuclear forensic analysis based upon this exercise is provided.
Approximately one curie of 171Tm (T1/2 = 1.92a) has been produced and purified for the purpose of making a nuclear target for the first measurements of its neutron
capture cross section. Target preparation consisted of three key steps: (1) material production; (2) separation and purification;
and (3) electrodeposition onto a suitable backing material. Approximately 1.5 mg of the target material (at the time of separation)
was produced by irradiating ca. 250 mg of its stable enriched 170Er lanthanide neighbour with neutrons at the ILL reactor in France. This production method resulted in a “difficult-to-separate”
1:167 mixture of near-neighboring lanthanides, Tm and Er. Separation and purification was accomplished using high-performance
liquid chromatography (HPLC), with a proprietary cation-exchange column (Dionex, CS-3) and alpha-hydroxyisobutyric acid (α-HIB)
eluent. This technique yielded a final product of ∼95% purity with respect to Tm. A portion (20 μg) of the Tm was electrodeposited
onto thin Be foil and delivered to the Los Alamos Neutron Science Center (LANSCE) for preliminary analysis of its neutron
capture cross section using the Detector for Advanced Neutron Capture Experiments (DANCE). This paper discusses the major
hurdles associated with the separation and purification step, including scale-up issues related to the use of HPLC for material
separation and purification of the target material from α-HIB and 4-(2-pyridylazo)resorcinol (PAR) colorant. 相似文献
A novel multi-process method for separating Eu from neighbouring lanthanides (Ln) has been developed that chemically reduces
Eu(III) to Eu(II) prior to solvent extraction of Ln(III) with thenoyltrifluoroacetone in benzene. This method is capable of
achieving higher purities (>99%) and separation yields than previously published multi-process methods that stabilize and
separate the reduced Eu(II) as a sulphate solid and is ideal for enriching materials of high-value. Results from a variety
of combinations of a chemical or electrochemical reduction process preceding a separation process using either ion-exchange
chromatography, reversed phase chromatography, or solvent extraction are discussed. 相似文献
Chemically selective chemisorbents are needed to monitor natural and engineered waters for anthropogenic releases of stable and radioactive contaminants. Here, a number of individual and mixtures of chemisorbents were investigated for their ability to extract select fission and activation product elements from marine and coastal waters, including Co, Zr, Ru, Ag, Te, Sb, Ba, Cs, Ce, Eu, Pa, Np, and Th. Conventional manganese oxide and cyanoferrate sorbents, including commercially available Anfezh and potassium hexacyanocobalt(II) ferrate(II) (KCFC), were tested along with novel nano-structured surfaces (known as Self Assembled Monolayers on Mesoporous Supports or SAMMS) functionalized with a variety of moieties including thiol, diphosphonic acid (DiPhos-), methyl-3,4 hydroxypyridinone (HOPO-), and cyanoferrate. Extraction efficiencies were measured as a function of salinity, organic content, temperature, flow rate and sample size for both synthetic and natural fresh and saline waters under a range of environmentally relevant conditions. The effect of flow rate on extraction efficiency, from 1 to 70 mL min(-1), provided some insight on rate limitations of mechanisms affecting sorption processes. Optimized mixtures of sorbent-ligand chemistries afforded excellent retention of all target elements, except, Ba and Sb. Mixtures of tested chemisorbents, including MnO(2)/Anfezh and MnO(2)/KCFC/Thiol (1-3 mm)-SAMMS, extracted 8 of the 11 target elements studied to better than 80% efficiency, while a mixture of MnO(2)/Anfezh/Thiol (75-150 μm)-SAMMS mixture was able to extract 7 of the 11 target elements to better than 90%. Results generated here indicate that flow rate should be less of a consideration for experimental design if sampling from fresh water containing variable amounts of DOM, rather than collecting samples from salt water environments. Relative to the capability of any single type of chemisorbent tested, optimized mixtures of several sorbents are able to increase the number of elements that can be efficiently and simultaneously extracted from natural waters. 相似文献
Journal of Radioanalytical and Nuclear Chemistry - Pacific Northwest National Laboratory (PNNL) has leveraged focused ion beam capability at their Category II Nuclear Facility to facilitate nuclear... 相似文献