Development of 225Ac Production from Low Isotopic Dilution 229Th.

The promise of 225Ac targeted alpha therapies has been on the horizon for the last two decades. TerraPower Isotopes are uniquely suited to produce clinically relevant quantities of 225Ac through the decay of 229Th. Herein, a rapid processing scheme to isolate radionuclidic and radioisotopically pure 225Ac in good yield (98%) produced from 229Th that contains significant quantities of 228Th activity is described. The characterization of each step of the process is presented along with the detailed characterization of the resulting 225Ac isotopic starting material that will support the cancer research and development efforts.

Optical sensing of aqueous nitrate anion by a platinum(II) triimine salt based solid state material.

Selective and quantitative measurement of aqueous nitrate (NO3-) anion is achieved using solid [Pt(Cl-4-tpy)Cl]ClO4 salt (Cl-4-tpy = 4-chloro-2,2':6'2''-terpyridine), and as the salt supported on controlled porous glass. This detection method relies on the color change of the Pt(II) complex from yellow to red and intense luminescence response upon ClO4- exchange with NO3- due to concomitant enhancement of Pt⋯Pt interactions. The spectroscopic response is highly selective for NO3- over a large range of halides and oxoanions.

A highly sensitive, easy-and-rapidly-fabricable microfluidic electrochemical cell with an enhanced three-dimensional electric field.

An NP-µFEC is a reusable, novel microfluidic electrochemical cell with multiple non-planar interdigitated microelectrode arrays, minimal sample volume, and enhanced electric field penetration for highly sensitive electrochemical analysis. (i) The NP-µFEC features spatial 3-electrode architecture, and a small sample volume (∼4 µL). (ii) Here, [Fe(CN)6]3-/4- redox couple are used as an electrochemical reporter. The effects on the electrochemical properties of NP-µFEC due to the change in the reference electrode (RE) and counter electrode (CE)'s position with respect to the working electrode (WE) position are analyzed. For NP-µFEC, the position of the RE with respect to the WE does not affect the CV, DPV electrochemical profiles. However, the spacing between the CE and WE plays a significant role. (iii) The enhanced three-dimensional electric field penetration in NP-µFEC is validated by finite element analysis simulation using COMSOL Multiphysics. (iv) Without electrode surface modifications, NP-µFEC shows a detection limit (DL) of ∼2.54 × 10-6 M for aqueous [Fe(CN)6]3-/4- probe. (v) The DL for Cu2+, Fe3+, and Hg2+ are 30.5±9.5 µg L-1, 181±58.5 µg L-1, and 12.4±1.95 µg L-1, respectively, which meets the US Environmental Protection Agency (EPA)'s water contamination level for Cu, Fe, and is close to that for Hg (EPA limits are 1300 µg L-1, 300 µg L-1, and 2 µg L-1, respectively). (vi) Further, using a pressure-sensitive adhesive layer to form the channel and create the NP-µFEC configuration simplifies the manufacturing process, making it cost-effective and allowing for rapid adoption in any research lab. NP-µFEC is used to detect heavy metal ions in water. This demonstrates that cost-effective, easy-to-fabricate NP-µFEC can be a new sensitive electrochemical platform.

A microfluidic electrochemical cell for studying the corrosion of uranium dioxide (UO2).

We have developed a specialized microfluidic electrochemical cell that enables in situ investigation of the electrochemical corrosion of microgram quantities of redox active solids. The advantage of downscaling is the reduction of hazards, waste, expense, and greatly expanding data collection for hazardous materials, including radioactive samples. Cyclic voltammetry was used to monitor the oxidation-reduction cycle of minute quantities of micron-size uraninite (UO2) particles, from the formation of hexavalent uranium (U(vi)), U3O7 and reduction to UO2+x . Reaction progress was also studied in situ with scanning electron microscopy. The electrochemical measurements matched those obtained at the bulk-scale and were consistent with ex situ characterization of the run products by X-ray photoelectron spectroscopy, scanning transmission electron microscopy, and atomic force microscopy; thus, demonstrating the utility of the microfluidic approach for studying radioactive materials.

ESSENCE - A rapid, shear-enhanced, flow-through, capacitive electrochemical platform for rapid detection of biomolecules.

The rapid, sensitive, and selective detection of target analytes using electrochemical sensors is challenging. ESSENCE, a new Electrochemical Sensor that uses a Shear-Enhanced, flow-through Nanoporous Capacitive Electrode, overcomes current electrochemical sensors' response limitations, selectivity, and sensitivity limitations. ESSENCE is a microfluidic channel packed with transducer material sandwiched by a top and bottom microelectrode. The room-temperature instrument less integration process allows the switch of the transducer materials to make up the porous electrode without modifying the electrode architecture or device protocol. ESSENCE can be used to detect both biomolecules and small molecules by simply changing the packed transducer material. Electron microscopy results confirm the high porosity. In conjunction with the non-planar interdigitated electrode, the packed transducer material results in a flow-through porous electrode. Electron microscopy results confirm the high porosity. The enhanced shear forces and increased convective fluxes disrupt the electric double layer's (EDL) diffusive process in ESSENCE. This disruption migrates the EDL to high MHz frequency allowing the capture signal to be measured at around 100 kHz, significantly improving device timing (rapid detection) with a low signal-to-noise ratio. The device's unique architecture allows us multiple configuration modes for measuring the impedance signal. This allows us to use highly conductive materials like carbon nanotubes. We show that by combining single-walled carbon nanotubes as transducer material with appropriate capture probes, NP-µIDE has high selectivity and sensitivity for DNA (fM sensitivity, selective against non-target DNA), breast cancer biomarker proteins (p53, pg/L sensitivity, selective against non-target HER2).

pH-Mediated Colorimetric and Luminescent Sensing of Aqueous Nitrate Anions by a Platinum(II) Luminophore@Mesoporous Silica Composite.

Increased levels of nitrate (NO3-) in the environment can be detrimental to human health. Herein, we report a robust, cost-effective, and scalable, hybrid material-based colorimetric/luminescent sensor technology for rapid, selective, sensitive, and interference-free in situ NO3- detection. These hybrid materials are based on a square-planar platinum(II) salt [Pt(tpy)Cl]PF6 (tpy = 2,2';6',2″-terpyridine) supported on mesoporous silica. The platinum salt undergoes a vivid change in color and luminescence upon exposure to aqueous NO3- anions at pH ≤ 0 caused by substitution of the PF6- anions by aqueous NO3-. This change in photophysics of the platinum salt is induced by a rearrangement of its crystal lattice that leads to an extended Pt···Pt···Pt interaction, along with a concomitant change in its electronic structure. Furthermore, incorporating the material into mesoporous silica enhances the surface area and increases the detection sensitivity. A NO3- detection limit of 0.05 mM (3.1 ppm) is achieved, which is sufficiently lower than the ambient water quality limit of 0.16 mM (10 ppm) set by the United States Environmental Protection Agency. The colorimetric/luminescence of the hybrid material is highly selective to aqueous NO3- anions in the presence of other interfering anions, suggesting that this material is a promising candidate for the rapid NO3- detection and quantification in practical samples without separation, concentration, or other pretreatment steps.

Identification and Quantification of Technetium Species in Hanford Waste Tank AN-102.

Technetium-99 (Tc), a high yield fission product generated in nuclear reactors, is one of the most difficult contaminants to address at the U.S. Department of Energy Hanford, Savannah River, and other sites. In strongly alkaline solutions typifying Hanford tank waste, Tc exists as pertechnetate (TcO4-) (oxidation state VII) as well as in reduced forms (oxidation state < VII), collectively known as non-pertechnetate (non-TcO4-) species. Designing strategies for effective Tc management, including separation and immobilization, necessitates understanding the molecular structure of the non-TcO4- species and their identification in actual tank waste samples. Identification of non-TcO4- species would facilitate the development of new treatment technologies effective for dissimilar Tc species. Toward this objective, a spectroscopic library of the Tc(I) [fac-Tc(CO)3]+ and Tc(II, IV, V, VII) compounds was generated and applied to the characterization of the actual Hanford AN-102 tank waste supernatant, which was processed to adjust Na concentration to ∼5.6 M and remove 137Cs by spherical resorcinol-formaldehyde (sRF) ion-exchange resin. Post 137Cs removal, the cesium-loaded sRF column was eluted with 0.45 M HNO3. As-received AN-102, Cs-depleted effluent, and sRF eluate fractions were comprehensively characterized for chemical composition and speciation of Tc using 99Tc nuclear magnetic resonance spectroscopy and X-ray absorption spectroscopy. It was demonstrated for the first time that non-TcO4- Tc present in the AN-102 tank waste is composed of several low-valent Tc species, including the Tc(I) [fac-Tc(CO)3]+ and Tc(IV) compounds. This is the first demonstration of multiple non-TcO4- species co-existing in the Hanford tank waste, highlighting their importance for the waste processing.

Phase transformation induced mechanochromism in a platinum salt: a tale of two polymorphs.

Red crystals of [Pt(tpy)Cl]NO3·HNO3 show mechanochromic behaviour turning yellow when pressure is applied. The electronic character and spectroscopic signature of the red and yellow polymorphs change as a result of slipping of the molecular stacking planes in the solid state. The slippage alters the PtPt intermolecular distances from a linear stacked motif with <3.5 Å separations in the red polymorph to a less stacked motif of alternating short intradimer and long interdimer interactions in the yellow polymorph.

Probing the Radial Chemistry of Getter Components in Light Water Reactors via Controlled Electrochemical Dissolution.

Getters are among the key functional components in the tritium-producing burnable absorber rods (TPBARs) of light water reactors (LWRs) and are used to capture the released tritium gas. They are nickel-plated zircaloy-4 tubes that, upon exposure to irradiation or tritium in the light water reactors, undergo alteration in structure, chemical composition, and chemistry. Understanding the radial tritium distribution is key to gaining insight into the evolution of new chemistry upon irradiation to predict getter performance. The holy grail is to develop a method akin to selectively peeling off the layers of an onion in an effort to get a radial map of elements and particularly tritium across the getter. Toward this goal, the overall aim of this work is to establish a correlative technique that can be used to determine radial tritium distribution across getters. To this end, this work specifically focuses on the validation of a correlative method for controlled radial dissolution of nickel-plated getters. Here, pristine getters as well as getters loaded with different mass ratios of hydrogen and deuterium are used as the nonradioactive surrogates of tritium, the idea being that the methodology can be readily extended to tritiated getter components. Here, the surface nickel layers as well as the bulk zirconium layers are sequentially dissolved in a controlled, uniform way using voltage-assisted electrochemical dissolution techniques. The dissolution is complemented by periodic elemental analysis of the electrolyte solution during and post dissolution. This is complemented by microscopic analyses on the exposed surfaces to provide a correlative technique for a complete picture of the radial distribution of various elements across the getter.

Mechanisms of Plutonium Redox Reactions in Nitric Acid Solutions.

Plutonium (Pu) exhibits a complex redox behavior in aqueous solutions. This is due to the ability of the element to adapt a wide range of oxidation states typically from +3 to +6 and the tendency for dynamic interconversion between the oxidation states that primarily depend upon acid concentration and presence of coordinating ligands. This work interrogates the Pu redox behavior in aqueous nitric acid via a combination of voltammetry and in situ vis-NIR spectroelectrochemistry under controlled potentials to map the interconversion between the various Pu oxidation states. The NIR-spectroelectrochemistry studies used to complement the visible spectroscopy bring a new and more complete perspective into the plutonium redox transformations. This allows elucidation of the mechanisms of the involved redox reactions facilitating an in-depth understanding of the relative stability of the Pu oxidation states as a function of redox potentials and nitric acid concentrations. It is observed that oxidation of Pu(III) results in generation of Pu(IV) and Pu(VI) (the latter as PuO22+), bypassing the Pu(V) oxidation state. Further, with increasing acid concentrations, the formation of the Pu(VI) species progressively decreases so that the dynamic equilibrium between the Pu(III) and Pu(IV) oxidation states dominates. These findings have significant implications for developing separation processes for used nuclear fuel reprocessing and treatment.

Technetium immobilization by materials through sorption and redox-driven processes: A literature review.

The objective of this review is to evaluate materials for use as a barrier or other deployed technology to treat technetium-99 (Tc) in the subsurface. To achieve this, Tc interactions with different materials are considered within the context of remediation strategies. Several naturally occurring materials are considered for Tc immobilization, including iron oxides and low solubility sulfide phases. Synthetic materials are also considered, and include tin-based materials, sorbents (resins, activated carbon, modified clays), layered double hydroxides, metal organic frameworks, cationic polymeric networks and aerogels. All of the materials were evaluated for their potential in-situ and ex-situ performance with respect to long-term Tc uptake and immobilization, environmental impacts and deployability. Other factors such as the technology maturity, cost and availability were also considered. Given the difficulty of evaluating materials under different experimental conditions (e.g., solution chemistry, redox conditions, solution to solid ratio, Tc concentration etc.), a subset of these materials will be selected, on the basis of this review, for subsequent standardized batch loading tests.

Redox-Based Electrochemical Affinity Sensor for Detection of Aqueous Pertechnetate Anion.

Rapid, selective, and in situ detection of pertechnetate (TcO4-) in multicomponent matrices consisting of interfering anions such as the ubiquitous NO3- and Cl- or the isostructural CrO42- is challenging. Present sensors lack the selectivities to exclude these interferences or the sensitivities to meet detection limits that are lower than the drinking water standards across the globe. This work presents an affinity-based electrochemical sensor for TcO4- detection that relies on selective reductive precipitation of aqueous TcO4- induced by a 1,4-benzenedimethanethiol capture probe immobilized on an electrode platform. This results in a direct decrease in the electron transfer current, the magnitude of the decrease being proportional to the amount of TcO4- added. Using this approach, a detection limit of 1 × 10-10 M was achieved, which is lower than the drinking water standard of 5.2 × 10-10 M set by United States Environmental Protection Agency. The proposed approach shows selectivity to the TcO4- anion, allowing detection of TcO4- from a multicomponent groundwater sample obtained from a well at the Hanford site in Washington (well 299-W19-36) that also contained NO3-, Cl-, and CrO42-, without discernably affecting the detection limits.

Metal-Organic Framework-Based Microfluidic Impedance Sensor Platform for Ultrasensitive Detection of Perfluorooctanesulfonate.

The growing global concerns to public health from human exposure to perfluorooctanesulfonate (PFOS) require rapid, sensitive, in situ detection where current, state-of-the-art techniques are yet to adequately meet sensitivity standards of the real world. This work presents, for the first time, a synergistic approach for the targeted affinity-based capture of PFOS using a porous sorbent probe that enhances detection sensitivity by embedding it on a microfluidic platform. This novel sorbent-containing platform functions as an electrochemical sensor to directly measure PFOS concentration through a proportional change in electrical current (increase in impedance). The extremely high surface area and pore volume of mesoporous metal-organic framework (MOF) Cr-MIL-101 is used as the probe for targeted PFOS capture based on the affinity of the chromium center toward both the fluorine tail groups as well as the sulfonate functionalities as demonstrated by spectroscopic (NMR and XPS) and microscopic (TEM) studies. Answering the need for an ultrasensitive PFOS detection technique, we are embedding the MOF capture probes inside a microfluidic channel, sandwiched between interdigitated microelectrodes (IDµE). The nanoporous geometry, along with interdigitated microelectrodes, increases the signal-to-noise ratio tremendously. Further, the ability of the capture probes to interact with the PFOS at the molecular level and effectively transduce that response electrochemically has allowed us achieve a significant increase in sensitivity. The PFOS detection limit of 0.5 ng/L is unprecedented for in situ analytical PFOS sensors and comparable to quantification limits achieved using state-of-the-art ex situ techniques.

Evaluation of materials for iodine and technetium immobilization through sorption and redox-driven processes.

Radioactive iodine-129 (129I) and technetium-99 (99Tc) pose a risk to groundwater due to their long half-lives, toxicity, and high environmental mobility. Based on literature reviewed in Moore et al. (2019) and Pearce et al. (2019), natural and engineered materials, including iron oxides, low-solubility sulfides, tin-based materials, bismuth-based materials, organoclays, and metal organic frameworks, were tested for potential use as a deployed technology for the treatment of 129I and 99Tc to reduce environmental mobility. Materials were evaluated with metrics including capacity for IO3- and TcO4- uptake, selectivity and long-term immobilization potential. Batch testing was used to determine IO3- and TcO4- sorption under aerobic conditions for each material in synthetic groundwater at different solution to solid ratios. Material association with IO3- and TcO4- was spatially resolved using scanning electron microscopy and X-ray microprobe mapping. The potential for redox reactions was assessed using X-ray absorption near edge structure spectroscopy. Of the materials tested, bismuth oxy(hydroxide) and ferrihydrite performed the best for IO3-. The commercial Purolite A530E anion-exchange resin outperformed all materials in its sorption capacity for TcO4-. Tin-based materials had high capacity for TcO4-, but immobilized TcO4- via reductive precipitation. Bismuth-based materials had high capacity for TcO4-, though slightly lower than the tin-based materials, but did not immobilize TcO4- by a redox-drive process, mitigating potential negative re-oxidation effects over longer time periods under oxic conditions. Cationic metal organic frameworks and polymer networks had high Tc removal capacity, with TcO4- trapped within the framework of the sorbent material. Although organoclays did not have the highest capacity for IO3- and TcO4- removal in batch experiments, they are available commercially in large quantities, are relatively low cost and have low environmental impact, so were investigated in column experiments, demonstrating scale-up and removal of IO3- and TcO4- via sorption, and reductive immobilization with iron- and sulfur-based species.

Understanding Time Dependence on Zinc Metal-Organic Framework Growth Using in Situ Liquid Secondary Ion Mass Spectrometry.

The abundance of novel metal-organic framework (MOF) materials continues to increase as more applications are discovered for these highly porous, well-ordered crystalline structures. The simplicity of constituents allows for the design of new MOFs with virtue of functionality and pore topology toward target adsorbates. However, the fundamental understanding of how these frameworks evolve during nucleation and growth is mostly limited to speculation from simulation studies. In this effort, we utilize a unique vacuum compatible system for analysis at the liquid vacuum interface (SALVI) microfluidic interface to analyze the formation and evolution of the benchmark MOF-74 framework using time-of-flight secondary ion mass spectrometry (ToF-SIMS). Principal component analysis of the SIMS mass spectra, together with ex situ electron microscopy, powder X-ray diffractometry, and porosimetry, provides new insights into the structural growth, metal-oxide cluster formation, and aging process of Zn-MOF-74. Samples collected over a range of synthesis times and analyzed closely with in situ ToF-SIMS, transmission electron microscopy, and gas adsorption studies verify the developing pore structure during the aging process.

A digital imaging method for evaluating the kinetics of vapochromic response.

This work describes the novel use of a cell phone camera and the L*a*b method (color space defined by the International Commission on Illumination) to characterize the color change in different vapochromic platinum(II) complexes in order to get quantitative and more reliable data. In this study, we have developed a semi-automatic CCA software that digitally analyzes images (e.g., video frames) collected while a vapochromic material is absorbing vapor and changing its color. The advantages of using this method, compared to reflectance or transmission spectroscopy through a thin film, include its low cost, convenience, portability, ease of sample preparation, the lack of need for specialized equipment, and the possibility of simultaneously collecting data on different samples under identical conditions. The results show that this strategy is effective in producing quantitative information about the kinetics of processes.

Iodine immobilization by materials through sorption and redox-driven processes: A literature review.

Radioiodine-129 (129I) in the subsurface is mobile and limited information is available on treatment technologies. Scientific literature was reviewed to compile information on materials that could potentially be used to immobilize 129I through sorption and redox-driven processes, with an emphasis on ex-situ processes. Candidate materials to immobilize 129I include iron minerals, sulfur-based materials, silver-based materials, bismuth-based materials, ion exchange resins, activated carbon, modified clays, and tailored materials (metal organic frameworks (MOFS), layered double hydroxides (LDHs) and aerogels). Where available, compiled information includes material performance in terms of (i) capacity for 129I uptake; (ii) long-term performance (i.e., solubility of a precipitated phase); (iii) technology maturity; (iv) cost; (v) available quantity; (vi) environmental impact; (vii) ability to emplace the technology for in situ use at the field-scale; and (viii) ex situ treatment (for media extracted from the subsurface or secondary waste streams). Because it can be difficult to compare materials due to differences in experimental conditions applied in the literature, materials will be selected for subsequent standardized batch loading tests.

Insight into Fluorocarbon Adsorption in Metal-Organic Frameworks via Experiments and Molecular Simulations.

The improvement in adsorption/desorption of hydrofluorocarbons has implications for many heat transformation applications such as cooling, refrigeration, heat pumps, power generation, etc. The lack of chlorine in hydrofluorocarbons minimizes the lasting environmental damage to the ozone, with R134a (1,1,1,2-tetrafluoroethane) being used as the primary industrial alternative to commonly used Freon-12. The efficacy of novel adsorbents used in conjunction with R134a requires a deeper understanding of the host-guest chemical interaction. Metal-organic frameworks (MOFs) represent a newer class of adsorbent materials with significant industrial potential given their high surface area, porosity, stability, and tunability. In this work, we studied two benchmark MOFs, a microporous Ni-MOF-74 and mesoporous Cr-MIL-101. We employed a combined experimental and simulation approach to study the adsorption of R134a to better understand host-guest interactions using equilibrium isotherms, enthalpy of adsorption, Henry's coefficients, and radial distribution functions. The overall uptake was shown to be exceptionally high for Cr-MIL-101, >140 wt% near saturation while >50 wt% at very low partial pressures. For both MOFs, simulation data suggest that metal sites provide preferable adsorption sites for fluorocarbon based on favorable C-F ··· M+ interactions between negatively charged fluorine atoms of R134a and positively charged metal atoms of the MOF framework.

Probing the Sorption of Perfluorooctanesulfonate Using Mesoporous Metal-Organic Frameworks from Aqueous Solutions.

One approach to reduce increasing concentrations of toxic per- and polyfluoroalkyl substances (PFAS) involves the capture of PFAS from aqueous media using porous materials. The use of highly porous, tunable metal organic framework (MOF) materials is appealing for targeted liquid phase sorption. In this work, we demonstrate the excellent capture of perfluorooctanesulfonate (PFOS) using both the chromium and iron analogs of the MIL-101 framework. Experimental characterization of PFOS uptake reveals unique differences in sorption properties between these two analogs, providing key implications for future PFOS sorbent design. Specifically, STEM-EDS and IR spectroscopy show definitive proof of sorption. Furthermore, XPS analysis shows evidence of a strong interaction between sulfur atoms of the polar headgroup of PFOS and the metal center of the framework in addition to the fluorinated nonpolar tail. Additionally, in situ 19F NMR reveals higher PFOS affinity for Cr-MIL-101 versus Fe-MIL-101 based on sorption kinetics. Surprisingly, at these relatively high PFOS concentrations, activated acetylene black carbon is severely outperformed by both MOFs.

An electrochemical technique for controlled dissolution of zirconium based components of light water reactors.

Zircaloy-4 (Zr-4) based liners and getters are the principle functional components of Tritium-Producing Burnable Absorber Rods (TPBARs) in light water nuclear reactors where they reduce tritiated water into tritium gas. Upon tritium exposure, zirconium tritide is formed, which changes the chemical composition, structure and morphology of these materials. Their thermodynamic properties are affected by (i) the hydride phase identity, (ii) radial and spatial tritide/hydride (T/H) distribution, and (iii) the changes in structure and morphology of the material upon T/H-migration, and their comprehensive knowledge is needed to predict performance of these materials. This work demonstrates that controlled potential electrochemistry techniques to be highly efficient for controlled oxidative radial dissolution of Zr-4 based liners (both unloaded and loaded with hydride/deuteride as chemical surrogates for tritium). The electrodissolution is further combined with microscopic techniques to accurately determine the distribution of hydride phases. This work demonstrates a reliable technique for radially etching the liners after irradiation to provide insight into the radial and spatial distribution of tritium within the TPBAR, improving the fundamental understanding of tritium transport and providing a basis for validating predictive models.