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Eiden, Gregory C.

Publications and source records attributed to Eiden, Gregory C..

At least 19 records
All sourcesNASA NTRSDOE OSTI
DOE OSTI2023

Utilizing metal cation reactions with carbonyl sulfide to remove isobaric interferences in tandem inductively coupled plasma mass spectrometry analyses

Carbonyl sulfide (OCS) was used as a reaction gas to investigate gas phase metal (M + ) ion-molecule reactions using the Agilent 8900 inductively coupled plasma tandem mass spectrometer (ICP-MS/MS) to yield insight on how this gas may be used to remove isobaric interferences in analytical measurements. The experimental work was paired with density functional theory (DFT) calculations of the reaction enthalpy to predict whether M + will react with OCS. A multi-element standard containing 46 elements ranging from 9 to 208 u was analyzed in the presence and absence of OCS. When a reaction was observed, the dominant product was the sulfide (MS + ). Oxide products were also observed for many M + but formation was less efficient with OCS than previously observed with other reaction gases. This is likely due to the weaker OC-S bond that makes MS + formation more favorable. Increasing the flow rate from 0.1 to 0.2 mL/min (corresponding to a change in reaction gas pressure from 0.35 to 0.53 Pa (2.6 to 4.0 mTorr)) generally resulted in greater MS + production, including the secondary product MS 2 + for a few cations. The early lanthanide series ions (La + , Ce + , Pr + and Nd + ) produced greater quantities of MO + at the higher pressure, although MS + products were still the dominant product. The DFT-predicted reaction enthalpies were consistent with the observed sulfide formation, with an accuracy >90%; however, model predictions were less accurate for the minor and higher order products (< 77% for MO + ). Finally, the work presented here continues a systematic study of ion-molecule reactions in ICP-MS/MS to understand and develop new and novel ways to analyze complex mixtures with minimal pre-analysis treatment.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2022

Gas‐Phase Ion‐Molecule Interactions in a Collision Reaction Cell with ICP‐MS / MS : Investigations with CO 2 as the Reaction Gas

Carbon dioxide (CO 2 ) was used as a reaction gas to investigate the gas‐phase ion‐molecule interactions using the Agilent 8900 ICP‐MS/MS. A solution containing forty‐five elements representative of the periodic table was used to supply the ions to react with CO 2 in the collision/reaction cell (CRC). The only significant product ions formed were monoxides. The general reactivity was shown to be consistent with density functional theory (DFT)‐predicted reaction enthalpies, such that all predicted exothermic reactions produced product ions at levels of at least 1% of the unreacted ion. Most endothermic reactions observed had sufficient kinetic energy in excess of the reaction enthalpies. Our results suggest that reaction enthalpy is a reasonable predictor of reactivity with CO 2 on the timescales of the interactions in non‐thermal ICP‐MS/MS systems. The ease and rapidity of data collection with the ICP‐MS/MS and DFT calculations using the NWChem suite has value given the scarcity of thermochemical data of CO 2 reactions in the literature. These studies are especially useful for the identification of targeted reaction chemistries to be leveraged for analytical method development, such as for the inline separation of isobaric interferences from analytes of interest.

36 MATERIALS SCIENCE↗
DOE OSTI2022

Reduction of detection limit and quantification uncertainty due to interferent by neural classification with abstention

Many measurements in the physical sciences can be cast as counting experiments, where the number of occurrences of a physical phenomenon informs the prevalence of the phenomenon's source. Often, detection of the physical phenomenon (termed signal) is difficult to distinguish from naturally occurring phenomena (termed background). In this case, the discrimination of signal events from background can be performed using classifiers, and they may range from simple, threshold-based classifiers to sophisticated neural networks. These classifiers are often trained and validated to obtain optimal accuracy, however we show that the optimal accuracy classifier does not generally coincide with a classifier that provides the lowest detection limit, nor the lowest quantification uncertainty. Here, we present a derivation of the detection limit and quantification uncertainty in the classifier-based counting experiment case. We also present a novel abstention mechanism to minimize the detection limit or quantification uncertainty a posteriori. We illustrate the method on two data sets from the physical sciences, discriminating Ar-37 and Ar-39 radioactive decay from non-radioactive events in a gas proportional counter, and discriminating neutrons from gammas in an inorganic scintillator and report results therefrom.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗
DOE OSTI2021

Gas-phase ion-molecule interactions in a collision reaction cell with triple quadrupole-inductively coupled plasma mass spectrometry: Investigations with N 2 O as the reaction gas

Nitrous oxide (N 2 O) was used as a reaction gas to investigate the gas phase ion-molecule interactions using the Agilent 8900 QQQ-ICP-MS. A multi-element standard containing 45 elements with masses ranging from 9 to 208 u was measured in the presence and absence of N 2 O. The main product ion species observed were oxides and nitrides. Comparison of the N 2 O reaction results with similar measurements conducted with O 2 revealed that N 2 O was more effective at forming oxides in general: the elements Cd and Pb were shown to produce oxides with N 2 O where the reaction did not occur with O 2 . Nitrous oxide was also shown to produce a significant amount of nitride species in a few cases. The general reactivity was shown to be consistent with density functional theory (DFT)-predicted reaction enthalpies, such that all predicted exothermic reactions produced product ions at levels at least 1% of the unreacted ion. Our results show that reaction enthalpy is a reasonable predictor of reactivity with N2O on the timescales of the interactions in non-thermal ICP-MS/MS systems. Our work demonstrates the utility of two relatively new platforms (commercial elemental ICP-MS/MS and EMSL Arrows interface to the NWChem program suite), which allows for the study of a large number of elements within a short period. While DFT with the basis sets utilized here is not the most accurate computational method, it is also not computationally expensive and is shown to be suitable for predicting gas phase reactivity in the QQQ-ICP-MS for the majority of ions studied. Here, the ease and rapidity of data collection and DFT calculations has the potential to be very impactful for the identification of targeted reaction chemistries to be leveraged for analytical method development, such as for the inline separation of isobaric interferences from analytes of interest.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2020

Analytical Determination of Radioactive Strontium and Cesium by Thermal Ionization Mass Spectrometry

Thermal ionization mass spectrometry (TIMS) has been evaluated for the detection of the radioactive isotopes of strontium and cesium. The instrument was investigated for the analysis of isotopic ratios of 89Sr to 90Sr and 135Cs to 137Cs in the presence of atomic isobars (Y and Zr for Sr analysis and Ba for Cs analysis). Signicant discrimination using TIMS was found for both Sr and Cs through evaluation using stable isotopes. Fusion procedures with different flux were evaluated for preparation of sample matrices. Chemical separations were developed and used after fusion to isolate the Sr and Cs from a prepared background matrix (i.e., Montana Soil). A graded approach, increasing in stable background isotopes, was performed to monitor the chemistry and instrument response. A thermal neutron irradiation was performed to produce a sample that contained the radioisotopes of Sr and Cs. Even though the irradiated sample was not a certified standard it does provide accurate expectation values via published, well understood cumulative fission yield data. The results presented in this work correlate extremely well with the published data. Furthermore, a significant decrease in uncertainty (by a factor of 5 { 10) was found for the isotopic ratios measured with TIMS compared to the published values.

TIMS, environmental contamination, radiostrontium,↗
DOE OSTI2019

Enhanced Ion Detection for Atomic Mass Spectrometry

In atomic mass spectrometry, polyatomic interferences that obscure ions of interest are a serious concern and in many cases hamper, or make impossible, the measurement of low signal analytes. Electron multipliers in pulse counting mode are used prolifically when low intensity ion beams are present during analysis as they provide on the order of 106-107 signal amplification, however simply counting the number of electron pulses ignores differences in the impact physics that are present depending on ion identity. The objective of this research was to investigate the efficacy of utilizing advanced neural network analysis and machine learning to recognize the differences in the analog electron multiplier pulse shapes for atomic vs. polyatomic ions of similar or identical mass as a means of distinguishing the two ion types. In this work, we’ve successfully discriminated polyatomic interferants from atomic analytes of interest for two different mass spectrometers, and three different ion pairs; Krypton isotope/hydride and methane/oxygen (noble gas mass spectrometer) and 129I atomic vs 129I polyatomic (Triton mass spectrometer). Discrimination accuracy for these experiments ranged from 76% to 95%.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗
DOE OSTI2019

Quantifying Low Energy ICP-MS Isotope Deposition

Mass spectrometry (MS) offers an alternative approach to chemical or chromatographic separations to selectively isolate and collect individual isotopes of an element for analytical purposes. During this MS isotopic isolation process, the amount of material deposited on to a target can be conveniently tracked by measuring ion current or accumulated charge. In this paper we report the first study comparing measurment of isotope deposition amount with separated isotope ion current for isotopes of six different elements (88Sr, 107Ag, 133Cs, 140Ce, 175Lu and 205Tl). These isotopes were sequentially deposited on a conductive substrate located in place of the standard electron multiplier in a quadrupole inductively coupled plasma MS. The results indicate good correlation between measured ion current and deposited mass as measured by quantitative analysis. This empirically confirms a means to quantify total mass deposition by ion charge measurements at implantation energies of 5 – 10 eV.

Liezers, Martin↗
DOE OSTI2019

Quantification techniques of mass-separation and ion yield for the detection of radioactive isotopes

This research demonstrates two methods of quantifying isotope separation efficiency using an inductively coupled plasma mass spectrometer. One method measured the accumulated charge on a conductive collection substrate in real-time while the second method performed a chemical dissolution of the substrate with subsequent post-processing and analysis. Our previous results demonstrated and compared these methods with a multi-element standard of stable isotopes. This research applies these methods to quantifying radioactive isotopes utilizing measurements of the stable isotope at the same mass-to-charge ratio. The mass-separated radioactive isotope were fission products produced from thermal neutron irradiation of a highly enriched 235U foil. The two methods are explained and the results of this new separation methodology are compared to available cumulative fission yields.

Dion, Michael P.↗
DOE OSTI2018

Simulating the effects of underground nuclear explosions with an exploding wire

Exploding wires can deposit significant amounts of energy (1000’s of Joules on a nano-microsecond timescales) into a very confined space. Under the right conditions they can even produce neutrons. While most exploding wire studies have been performed in open air and to a lesser extent liquids we have started to investigate enclosing the wire element in solid matrices like concrete to mimic the effects of an underground nuclear explosion. The temperatures and pressures achieved are quite sufficient to induce structural cracking and localized flash melting in the enclosing media like a real underground nuclear detonation. As a result exploding wires would appear to form the perfect trigger for releasing confined chemical species including gases in geological media to study migration behavior in a controlled environment. Details of the apparatus and some illustrations of it potential will be given.

Underground Nuclear Explosions, Exploding Wires, X↗
DOE OSTI2017

Characterization of extreme ultraviolet laser ablation mass spectrometry for actinide trace analysis and nanoscale isotopic imaging

The purpose of this research was to characterize Extreme Ultraviolet Time-of-Flight (EUV TOF) Laser Ablation Mass Spectrometry for high spatial resolution elemental and isotopic analysis. We compare EUV TOF results with Secondary Ionization Mass Spectrometry (SIMS) to orient the EUV TOF method within the overall field of analytical mass spectrometry. Using the well-characterized NIST 61x glasses, we show that the EUV ionization approach produces relatively few molecular ion interferences in comparison to TOF SIMS. We demonstrate that the ratio of element ion to element oxide ion is adjustable with EUV laser pulse energy and that the EUV TOF instrument has a sample utilization efficiency of 0.014%. The EUV TOF system also achieves a lateral resolution of 80 nm and we demonstrate this lateral resolution with isotopic imaging of closely spaced particles or uranium isotopic standard materials.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗
DOE OSTI2016

The Preparation of Non-radioactive Glassy Surrogate Nuclear Explosion Debris (SNED) Loaded with an Isotopically Altered Noble Gas

The measurement of the Kr and Xe isotope ratios in nuclear explosion debris is an important forensic tool as the method requires very little sample preparation. Fragments of debris are simply crushed or heated to release the trapped gases Kr and Xe arising from fission product decay. As suitable test materials are not readily available we have been investigating a method to incorporate isotopically enriched 129Xe in glassy materials that mimic nuclear explosion debris. The approach used to prepare these materials will be described along with some of the example results obtained.

Trinitite, Nuclear forensics, Fission Xe, Surrogat↗
DOE OSTI2016

Measurement Background and the Sediment Age-Dating Reach of 32Si

Silicon-32 has been identified as an isotope that fills the sediment geochronology gap created between Pb-210 at <150 years and C-14 at >1000 years. However, detector sensitivity and chemical isolation challenges of radiometric Si-32 for age dating have resulted in a fairly limited number of applications of this technique to real-world sediment studies. The significance of targeting the intermediate age bracket is to provide accurate geochronological reconstructions of paleoindicators that identify human and large-scale, climate-induced shifts in coastal areas. Therefore, we targeted Puget Sound, Washington, United States, to demonstrate the application of Si-32 age dating to determine the relative importance of climate cycles versus human activities in an in-land sea. The enhanced reconstructions will be achieved through the design of new detectors, chemical separation of biogenic silica from kilogram-scale sediment samples, and demonstration of the viable age-dating reach of Si-32. Implications of detector background on the duration of required measurements and the age-dating reach are considered. The design of a low-background, gas-proportional beta counter for measurement of the daughter isotope P-32 is discussed; detector background goals for these new detectors are based on the sensitivity study.

Keillor, Martin E.↗
DOE OSTI2016

Identification of Uranyl Minerals Using Oxygen K-Edge X Ray Absorption Spectroscopy

Uranium analysis is consistently needed throughout the fuel cycle, from mining to fuel fabrication to environmental monitoring. Although most of the world’s uranium is immobilized as pitchblende or uraninite, there exists a plethora of secondary uranium minerals, nearly all of which contain the uranyl cation. Analysis of uranyl compounds can provide clues as to a sample’s facility of origin and chemical history. X-ray absorption spectroscopy is one technique that could enhance our ability to identify uranium minerals. Although there is limited chemical information to be gained from the uranium X-ray absorption edges, recent studies have successfully used ligand NEXAFS to study the physical chemistry of various uranium compounds. This study extends the use of ligand NEXAFS to analyze a suite of uranium minerals. We find that major classes of uranyl compounds (carbonate, oxyhydroxide, silicate, and phosphate) exhibit characteristic lineshapes in the oxygen K-edge absorption spectra. As a result, this work establishes a library of reference spectra that can be used to classify unknown uranyl minerals.

Environmental Molecular Sciences Laboratory↗
DOE OSTI2016

The influence of ns- and fs-LA plume local conditions on the performance of a combined LIBS/LA-ICP-MS sensor

Both laser-induced breakdown spectroscopy (LIBS) and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) are well-established analytical techniques with their own unique advantages and disadvantages. The combination of the two analytical methods is a very promising way to overcome the challenges faced by each method individually. We made a comprehensive comparison of local plasma conditions between nanosecond (ns) and femtosecond (fs) laser ablation (LA) sources in a combined LIBS and LA-ICP-MS system. The optical emission spectra and ICP-MS signal were recorded simultaneously for both ns- and fs-LA and figures of merit of the system were analyzed. Characterization of the plasma was conducted by evaluating temperature and density of the plume under various irradiation conditions using optical emission spectroscopy, and correlations to ns- and fs-LIBS and LA-ICP-MS signal were made. The present study is very useful for providing conditions for a multimodal system as well as giving insight into how laser ablation plume parameters are related to LA-ICP-MS and LIBS results for both ns- and fs-LA.

LaHaye, Nicole L.↗