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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 1,027 records · Page 57
All sourcesNASA NTRSDOE OSTI
DOE OSTI2012

Experiments with the LECO Pegasus® Gas Chromatograph/ Time-of-Flight Mass Spectrometer Phase 2: 2D Fast GC Separations

Conventional analysis by gas chromatography/ quadrupole mass spectrometry (GC/MS) can be time-consuming (30 – 60 minutes) and prone to interferences. The use of fast gas chromatography coupled with time-of-flight mass spectrometry (GC/TOF-MS) offers the advantages of faster (~10 min) analysis times, improved GC resolution afforded by the use of narrower (0.1– 0.18 mm id) columns, and improved mass resolution and scan speed provided by the TOF-MS. In addition, GC/TOF-MS offers the promise of better instrument detection limits than quadrupole GC/MS, while still providing full mass spectral data. If the GC/TOF-MS can be operated to perform two-dimensional (2D) separations, the ability to resolve peaks of interest from interfering compounds is improved. In 2D chromatography, a second GC column with a different chemical phase than that of the first GC column is used to provide additional separation of analytes as they elute from the first column. Because the chemistry of the second GC column is different from the first, compounds that co-elute from the first column may be easily resolved after a separation on the second GC column (i.e., the peak capacity of the system is increased and the specificity of analyte detection is improved).

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2013

Neutron Leakage Spectrum from a Pulsed Uranium Sphere [Slides]

The neutron leakage spectrum from a pulsed uranium sphere was calculated with MCNP5 and found to be in good agreement with previous “MCN” simulations and experimental data. This example is proposed as another time-of-flight (TOF) test problem for NUEXS, a code for diagnostic simulation maintained by LANL Group P-23.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2014

Photocopia-A Unibody Mono-material Compact and Scalable Photomultiplier

The Photocopia photomultiplier tube (PMT) takes advantage of two of the many unique properties of the hydrogenated amorphous silicon-germanium (a-SiGe) photoemitter material: its mechanical flexibility and mostly substrate-independent properties. The a-SiGe photoemitter has high secondary electron (SE) yield. It can be used both as the photocathode and as the gain medium. The active material can be grown on a flat, thin unibody substrate, formed and then “rolled up” ex situ. The completed structure would then be activated and sealed within a tube. The Ge component can be increased to enhance red-sensitivity. Compact sizes are possible, minimizing magnetic field effects. The Photocopia PMT will be a low cost alternative to MCPs for TOF detectors and provide better timing discrimination for Cherenkov detectors. Retention of the ability to activate to a normal photoyield state upon flexing (bending) the substrate of the a-SiGe material after growth, but prior to activation has been shown. The SE coefficient of the activated material has been characterized over the voltage range suitable for utilization as the gain material. The time response of the material is suited to PMT use.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗
DOE OSTI2015

Basic Physics Data: Measurement of Neutron Multiplicity from Induced Fission

From October 1 to October 17 a team of researchers from UM visited the LANSCE facility for an experiment during beam-time allotted from October 4 to October 17. A total of 24 detectors were used at LANSCE including liquid organic scintillation detectors (EJ-309), NaI scintillation detectors, and Li-6 enriched glass detectors. It is a double time-offlight (TOF) measurement using spallation neutrons generated by a target bombarded with pulsed high-energy protons. The neutrons travel to an LLNL-manufactured parallel plate avalanche chamber (PPAC) loaded with thin U-235 foils in which fission events are induced. The generated fission neutrons and photons are then detected in a detector array designed and built at UM and shipped to LANSCE. Preparations were made at UM, where setup and proposed detectors were tested. The UM equipment was then shipped to LANSCE for use at the 15L beam of the weapons neutron research (WNR) facility.

43 PARTICLE ACCELERATORS↗
DOE OSTI2015

Generation, Detection and characterization of Gas-Phase Transition Metal containing Molecules

The objective of this project was to generate, detect, and characterize small, gas-phase, metal containing molecules. In addition to being relevant to high temperature chemical environments (e.g. plasmas and combustion), gas-phase experiments on metal containing molecules serve as the most direct link to a molecular-level theoretical model for catalysis. Catalysis (i.e. the addition of a small about of recoverable material to control the rate and direction of a chemical reaction) is critical to the petroleum and pharmaceutical industries as well as environmental remediation. Currently, the majority of catalytic materials are based on very expensive metals such as platinum (Pt), palladium (Pd), iridium (Ir,) rhenium (Re), and rhodium (Rh). For example, the catalyst used for converting linear hydrocarbon molecules (e.g. hexane) to cyclic molecules (e.g. cyclohexane) is a mixture of Pt and Re suspended on alumina. It enables straight chain alkanes to be converted into branched-chain alkanes, cyclohexanes and aromatic hydrocarbons which are used, amongst other things, to enhance the octane number of petrol. A second example is the heterogeneous catalysis used in automobile exhaust systems to: a) decrease nitrogen oxide; b) reduce carbon monoxide; and c) oxidize unburned hydrocarbons. The exhaust is vented through a high-surface area chamber lined with Pt, Pd, and Rh. For example, the carbon monoxide is catalytically converted to carbon dioxide by reaction with oxygen. The research results from this work have been published in readily accessible journals1-28. The ground and excited electronic state properties of small metal containing molecules that we determine were: a) electronic state distributions and lifetimes, b) vibrational frequencies, c) bond lengths and angles, d) hyperfine interactions, e) permanent electric dipole moments, mel, and f) magnetic dipoles, μ m . In general terms, μ el , gives insight into the charge distribution and mm into the number and nature of the unpaired electrons. Analysis of the hyperfine interactions (i.e. Fermi-contact, nuclear electric quadrupole, etc.) is particularly insightful because it results from the interaction of nuclei with non-zero spin and the chemically important valence electrons. The bulk of the spectroscopic techniques used in these studies exploit the sensitivity of laser induced fluorescence (LIF) detection. The spectroscopic schemes employed include: a) cw and pulsed laser field-free(FF) excitation and dispersed LIF (DLIF); b) optical Stark; c) optical Zeeman; d) pump/probe microwave double resonance (PPMODR); e) fluorescence lifetimes, and f) resonant and non-resonant two-photon ionization TOF mass spectrometry. Vibrational spacing, force constants and electronic states distributions are derived from the analysis of pulsed dye laser excitation and DLIF spectra. Geometric structure (bond lengths and angles) and hyperfine parameters are derived from the analysis of cw-laser LIF and PPMODR spectra. Permanent electric dipole moments, mel,, and magnetic dipole moments, mm, are derived from the analysis of optical Stark and Zeeman spectra, respectively. Transition moments are derived from the analysis of radiative lifetimes. A supersonic molecular beam sample of these ephemeral molecules is generated by skimming the products of either a laser ablation/reaction source or a d.c. discharge source.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2016

GoAmazon2014/15. Oxidation Flow Reactor Final Campaign Report

The primary goal of the Green Ocean Amazon (GoAmazon2014/5) field campaign was to measure and mechanistically understand the formation of particle number and mass in a region affected by large tropical rainforest biogenic emissions and sometimes anthropogenic influence from a large urban center. As part of the two intensive operational periods (IOPs) and in collaboration with Pacific Northwest National Laboratory (PNNL) and Harvard, the Jimenez Group proposed to deploy a High-Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS), Thermal Denuder (TD), Scanning Mobility Particle Size (SMPS), two oxidation flow reactors (OFR; including supporting O 3 , CO/CO 2 /CH 4 , RH analyzers), and a high volume filter sampler (MCV) for the measurement of gas and aerosol chemical, physicochemical, and volatility properties. The two IOPs were conducted during the wet season (February to March, 2014) and dry season (August to October, 2014). This proposal was part of a collaborative proposal involving other university and government laboratories.

54 ENVIRONMENTAL SCIENCES↗
DOE OSTI2015

A Study of Particle Production in Proton Induced Collisions Using the MIPP Detector at Fermilab

The Main Injector Particle Production (MIPP) experiment is a fixed target hadron production experiment at Fermilab. MIPP is a high acceptance spectrometer which provides excellent charged particle identification using Time Projection Chamber (TPC), Time of Flight (ToF), multicell Cherenkov (Ckov), ring imaging Cherenkov (RICH) detectors, and Calorimeter for neutrons. The MIPP experiment is designed to measure particle production in interactions of 120 GeV/c primary protons from the Main Injector and secondary beams of $\pi^{\pm}, \rm{K}^{\pm}$, p and $\bar{\rm{p}}$ from 5 to 90 GeV/c on nuclear targets which include H, Be, C, Bi and U, and a dedicated run with the NuMI target. The goal of the experiment is to measure hadron production cross sections or yields using these beams and targets. These hadronic interaction data can have a direct impact on the detailed understanding of the neutrino fluxes of several accelerator-based neutrino experiments like MINOS, MINER$\nu$A, NO$\ nu$A and ELBNF. In this thesis, we present inelastic cross section measurements for 58 and 85 GeV/c p+p interactions, and 58 and 120 GeV/c p+Be, p+C and p+Bi interactions. A new method is described to account for the low multiplicity inefficiencies in the interaction trigger using KNO scaling. Inelastic cross sections as a function of multiplicity are also presented for p+H and p+C interactions at different beam momenta. The MIPP data are compared with the Monte Carlo predictions and existing data. We also describe an algorithm to identify charged particles ($\pi^{\pm}/\rm{p}/\bar{\rm{p}}$ etc.), and present the inclusive charged pion production cross sections in bins of true momentum using 58 and 120 GeV/c p+C interactions for both the data and Monte Carlo.

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗
DOE OSTI2016

Green Ocean Amazon (GoAmazon) 2014/15. Semi-Volatile Thermal Desorption Aerosol Gas Chromatograph (SVTAG) Field Campaign Report

In areas where biogenic emissions are oxidized in the presence of anthropogenic pollutants such as SO2, NOx, and black carbon, it has become increasingly apparent that secondary organic aerosol (SOA) formation from biogenic volatile organic compounds (VOCs) is substantially enhanced. Research is urgently needed to elucidate fundamental processes of natural and anthropogenically influenced VOC oxidation and the contribution of these processes to SOA formation. GoAmazon 2014/15 afforded study of the chemical transformations in the region downwind of Manaus, Brazil, where local biogenic VOC emissions are high, and their chemical oxidation can be studied both inside and outside of the urban plume to differentiate the role of anthropogenic influence on secondary aerosol formation during oxidation of these natural VOC emissions. To understand the connection between primary biogenic VOC emissions and their secondary products that form aerosols, we made time-resolved molecular level measurements by deploying a Semi-Volatile Thermal Desorption Aerosol Gas Chromatograph (SV-TAG) and a sequential filter sampler during two intensive operational periods (IOPs) of the GoAmazon 2014/15 field campaign. The SV-TAG measured semi-volatile organic compounds in both the gas and particle phases and the sequential filter sampler collected aerosols on quartz fiber filters in four-hour increments used for offline analysis. SV-TAG employed novel online derivatization that provided chemical speciation of highly oxygenated or functionalized compounds that comprise a substantial fraction of secondary organic aerosols, yet are poorly characterized. It also provided partitioning of these compounds between the vapor and particle phases at sufficient time resolution to define the importance of competing atmospheric processes. These measurements were supported by offline analysis of the filters using two-dimensional gas chromatography (GC x GC) with high-resolution time-of-flight mass spectrometry (HR-TOF-MS) using both electron impact (EI) and soft vacuum ultraviolet (VUV) ionization with derivatization. Speciated chemical data from SV-TAG and filter measurements were used to elucidate the relative importance of potential oxidation pathways by providing detailed information on the product distribution from atmospheric reactions and the quantification of known tracers for various oxidation pathways. Together, these techniques provided unequivocal molecular identification of a wide range of atmospheric organic compounds spanning the volatile, semi-volatile, and non-volatile phases. This level of chemical characterization provided insight into the chemical and physical processes that control the atmospheric oxidation of biogenic VOC and subsequent formation of SOA.

54 ENVIRONMENTAL SCIENCES↗
DOE OSTI2016

Proton Transfer Time-of-Flight Mass Spectrometer

The Proton Transfer Reaction Mass Spectrometer (PTRMS) measures gas-phase compounds in ambient air and headspace samples before using chemical ionization to produce positively charged molecules, which are detected with a time-of-flight (TOF) mass spectrometer. This ionization method uses a gentle proton transfer reaction method between the molecule of interest and protonated water, or hydronium ion (H 3 O + ), to produce limited fragmentation of the parent molecule. The ions produced are primarily positively charged with the mass of the parent ion, plus an additional proton. Ion concentration is determined by adding the number of ions counted at the molecular ion’s mass-to-charge ratio to the number of air molecules in the reaction chamber, which can be identified according to the pressure levels in the reaction chamber. The PTRMS allows many volatile organic compounds in ambient air to be detected at levels from 10–100 parts per trillion by volume (pptv). The response time is 1 to 10 seconds.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2017

Photonuclear Contributions to SNS Pulse Shapes

Short-pulsed sources like the Spallation Neutron Source (SNS) and ISIS produce bursts of neutron pulses at rates of 10-60 Hz, with sub-microsecond proton pulses impacting on high-Z target materials. Moderators are grouped around the target to receive the fast neutrons generated from spallation reactions to moderate them effciently to thermal and sub-thermal energies and to feed narrow neutron pulses to neutron scattering instruments. The scattering instruments use the neutrons as a probe for material investigations, and make use of time-of-flight (TOF) methods for resolving the neutron energy. The energy resolution of scattering instruments depends on the narrow time-structure of the neutron pulses, while neutrons in the long tail of the emission time distributions can degrade the instrument performance and add undesired background to measurements. The SNS neutronics team is investigating a possible source term impacting the background at short-pulsed spallation sources. The ISIS TS2 project claims to have significantly reduced neutron scattering instrument background levels by the elimination or reduction of iron shielding in the target-moderator-reflector assembly. An alternative hypothesis, also proposed by ISIS, suggests that this apparent reduction arises from moving beamline shielding away from the neutron guide channels, reducing albedo down the beamlines. In both hypotheses, the background neutrons in question are believed to be generated by photonuclear reactions. If the background neutrons are indeed generated via photonuclear channels, then they are generated in a time-dependent fashion, since most of the high-energy photons capable of inducing photonuclear production are gone within a few microseconds following the proton pulse. To evaluate this e ect, we have enabled photonuclear reactions in a series of studies for the SNS first target station (FTS) taking advantage of its Monte Carlo model. Using a mixture of ENDF/B VII.0 and TENDL-2014 photonuclear cross sections available and the CEM03 physics model within MCNPX 2.6.0 in the simulation, we are able to estimate the impact of photoneutron production on both overall neutron production and delayed neutron production. We find that a significant number of photon-induced neutrons are produced a few milliseconds after the proton pulse, following prompt gamma emission through the capture of neutrons in the slowing-down and thermalization processes. We name these "slowing-down delayed neutrons" to distinguish them from either "activation-delayed neutrons" or "beta-delayed neutrons." The beta-delayed and activation-delayed neutrons were not part of this study, and will be addressed elsewhere. While these other delayed neutron channels result in the time-independent (constant) production of fast neutrons outside of the prompt pulse, the slowing-down delayed neutrons also a ect the shape of the pulses. Although numerically insignificant in most cases, we describe a set of scenarios related to T0-chopper operation in which the slowing-down delayed neutrons may be important.

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗
DOE OSTI2015

Identification of Chemical Attribution Signatures of Fentanyl Syntheses Using Multivariate Statistical Analysis of Orthogonal Analytical Data

Attribution of the origin of an illicit drug relies on identification of compounds indicative of its clandestine production and is a key component of many modern forensic investigations. The results of these studies can yield detailed information on method of manufacture, starting material source, and final product - all critical forensic evidence. In the present work, chemical attribution signatures (CAS) associated with the synthesis of the analgesic fentanyl, N-(1-phenylethylpiperidin-4-yl)-N-phenylpropanamide, were investigated. Six synthesis methods, all previously published fentanyl synthetic routes or hybrid versions thereof, were studied in an effort to identify and classify route-specific signatures. 160 distinct compounds and inorganic species were identified using gas and liquid chromatographies combined with mass spectrometric methods (GC-MS and LCMS/ MS-TOF) in conjunction with inductively coupled plasma mass spectrometry (ICPMS). The complexity of the resultant data matrix urged the use of multivariate statistical analysis. Using partial least squares discriminant analysis (PLS-DA), 87 route-specific CAS were classified and a statistical model capable of predicting the method of fentanyl synthesis was validated and tested against CAS profiles from crude fentanyl products deposited and later extracted from two operationally relevant surfaces: stainless steel and vinyl tile. This work provides the most detailed fentanyl CAS investigation to date by using orthogonal mass spectral data to identify CAS of forensic significance for illicit drug detection, profiling, and attribution.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2018

Multimetallic Systems for the Photocatalytic Production of Fuels from Abundant Sources

The reported findings herein are a result of a collaboration between the groups of Claudia Turro at The Ohio State University (DE-SC0010542) and Kim R. Dunbar at Texas A&M University (DE-SC0010721). The Turro and Dunbar groups jointly discovered that cationic d 7 –d 7 Rh 2 (II,II) complexes bridged by electron-donating formamidinate (form) ligands possess redox-active excited states that are relatively long-lived and can engage in charge transfer reactions. As part of the present grant we designed new complexes that exhibit strong absorption from the UV to ~800 nm. The Rh 2 (II,II) complexes under investigation are poised to undergo catalytic reduction of substrates because they are robust to changes in metal oxidation state, the two metals and the two diimine ligands, together with the non-innocent bridges, can be used to store redox equivalents, making these complexes capable of coupling one-electron events with multi-electron transformations. We discovered the electrocatalytic reduction of H + and CO 2 by complexes that are able to electrocatalytically reduce H + to H 2 with high turnover frequencies (TOFs) and overpotentials, η, of ~0.5 V,8 as well as to reduce CO 2 to HCOOH. We now have experimental evidence that both the production of H 2 from H + and HCOOH. The molecular catalysts are stable after the acid and/or CO 2 is consumed since electrocatalysis is restored at the same rate upon the addition of substrate to the cell.8,9 Moreover, we showed that the catalysis is not a result of a decomposition product deposited on the electrode, since placing an electrode from an active electrocatalytic solution into one that does not contain catalyst completely shuts down the reactivity. We are currently exploring the reactivity of these complexes in hydride transfer reactions with other substrates and in the presence of CO 2 and reducing agents, as well as attempting to grow single crystals for x-ray diffraction.

14 SOLAR ENERGY↗
DOE OSTI2019

Simulations of Neutron Time-of-Flight Method by Inelastic Scattering Carbon-12 using MCNP6 and Geant4

A neutron spectroscopy technique using neutron time-of-flight (TOF) with gamma tagging from inelastic scattering on carbon-12 was examined using MCNP6 and Geant4. Experimental data for the 12 C(n,n'$γ$) reaction from D. Spaargaren and C.C. Jonken was used to supplement the simulations due to their limitations with modeling correlated particles on an event-by-event basis. The MCNP and Geant4 models relied on different methods to determine the efficiencies and were compared against each other for validation of the results. The total efficiency of coincident detection as determined by MCNP is around 6.32E-11. That is, around 6 events will be detected per 100 billion source neutrons. It was found that the amount of neutrons which lose energy to elastic scattering is not negligible, and efforts to reconstruct the beam energy from the detected neutrons must take this into account. Running on 40 computer cores in multi-threading mode, the Geant4 model could simulate about half a billion source neutrons per hour. In the absence of biasing methods, Geant4 can not simulate the efficiency in any reasonable amount of time given current computing power. Further efforts will be made to introduce biasing to the simulation to verify the MCNP results.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2020

Report to NCSP on 2008 DANCE measurements of 233 U($\eta$,$\gamma$)

Uranium-233 plays an important role in the Th-U fuel cycle, with substantial production in the cycle. This cycle has been proposed as an alternative to the U-Pu fuel cycle due to its reduced production of transuranic elements. An accurate measurement of the 233 U($\eta$,$\gamma$) cross section is required by the National Criticality Safety Program (NCSP) to complete the neutron-induced cross section data, where experimental capture cross section data are scarce and were measured decades ago. The most recent capture cross section data available in the literature were measured in 2007 at the n_TOF facility (CERN); in the 60s measurements were performed at Rensselaer Polytechnic Institute (RPI) and at LANL. Finally, as reported by ORNL, a new evaluation with a revised (renormalized) fission cross section is needed on 233 U. The challenge for this measurement lies in the difficulty of measuring the capture cross section data in the competing fission background, as the fission cross section is around one order of magnitude larger than the capture cross section for 233 U. The accuracy of a capture cross section measurement depends on discrimination between $\gamma$’s produced in capture and fission reactions, for which an experimental setup combining capture and fission detectors is needed. For the ($\eta$,$\gamma$) cross section measurement at LANSCE, this discrimination is achieved by combining the Detector for Advanced Neutron Capture Experiments (DANCE), to measure $\gamma$’s from capture reactions, with a Parallel Plate Avalanche Counter (PPAC) to tag the $\gamma$’s produced by fission. This method was successfully used to measure 235 U and 239 Pu capture cross sections. In these measurements, the neutron capture cross section was determined in a large fission background well above 100 keV. As part of the NCSP nuclear data effort, we have looked at past DANCE measurements on 233 U($\eta$,$\gamma$) and evaluated whether existing data is adequate to apply this technique.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗
DOE OSTI2020

Study of Poly(ether ketone ketone) (PEKK): Outgassing Characteristics and Likely Residual Synthesis Impurities

In May-June, 2020, a study was conducted to characterize the outgassing properties of a series PEKK (Poly(ether ketone ketone)) samples using cryo-GC/MS headspace analysis. Three sets of samples were interrogated: sample group 1 consisted of 2 additively manufactured PEKK samples (PEKK "ole and "New") prepared by KCNSC from powder material from Solvay Specialty Polymers USA, LLC. Sample groups 2 and 3 consist of 5 PEKK powder types (used as feedstock for additive manufacturing processes) and 4 additively-manufactured PEKK material lots, respectively. Contrary to expectations, all samples of PEKK material were observed to outgas sulfur-containing compounds. Other analyses (EDS/EMA, GC-TOF/MS of PEKK sample extractions) confirmed the presence of sulfur in the PEKK bulk material. Specifically, Diphenyl sulfone (used as a reagent or high-temperature solvent in the synthesis of Polyaryletherketone or PAEK polymers) was observed in three of the powders and in both the PEKK "Old" and "New" samples, suggesting that the source of the sulfur can be traced to impurities in the material left over from the synthesis process.

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

Progress on Associate-Particle Imaging Algorithms, 2020

The present work describes progress on the development of imaging algorithms that use fast neutron signatures acquired using the associated-particle imaging (API) method. The present work complements ongoing work to develop neutron source and detector hardware to enable field inspection by investigating algorithms that are capable of discriminating between critical materials or extracting three-dimensional geometrical information from single-sided or transmission measurements. The present work is divided into three approaches:(1)Iterative reconstruction of inelastic gamma-ray emissions to perform three-dimensional time-of-flight imaging in a single view in either transmission or backscatter configurations. Iterative reconstruction enables image resolution better than the inherent TOF resolution.(2)Decomposition of registered neutron and x ray radiographs into an assumed material list for each pixel in the image.(3)Material identification using full spectral analysis that includes the emergent neutron and gamma ray energies, times, and angles.Progress for each approach is summarized for fiscal year 2020.

97 MATHEMATICS AND COMPUTING↗
DOE OSTI2021

Focused Ion Beam analysis of non radioactive samples [PowerPoint]

The presentation includes various images to illustrate the analysis. Helios G4 Plasma FIB: Xe ion columns mills material 30 times faster than Ga; Options include: Energy Dispersive Spectroscopy (EDS), Wavelength Dispersive spectroscopy (WDS) Electron backscattered Diffraction (EBSD), Time of Flight Sims (ToF SIMS), Inert gas/vacuum sample transfer system; Excels at micromachining and collecting 3D datasets using various detection systems.

42 ENGINEERING↗
DOE OSTI2022

Time-of-Flight Calculations with Multiple Beam Phase Monitors: Calibration, Jitter Analysis & Energy Measurement

This report describes time-of-flight (ToF) beam energy measurements with multiple phase monitors in a beam line with no acceleration. Measurement uncertainty is quantified via rigorous treatment of beam-based phase monitor calibration and jitter analysis of the accelerator system. Experimental results in the Superconducting Linac (SCL) of the Spallation Neutron Source (SNS) are presented.

43 PARTICLE ACCELERATORS↗