Generating ultradense pair beams using 400 GeV / c protons
Not Available
72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗
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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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Technique for the generation of quasi-isotropic 1-10 Kev proton fluxes.
Resolution and geometrical factor determination for isotropic proton fluxes by using pencil beam and measurements over many angles and positions
PROTON BEAM↗
Influence of the proton relay spacer on hydrogen electrocatalysis by cobalt hangman porphyrins
A cobalt hangman porphyrin system with a phenyl spacer between the porphyrin ring and an internal carboxylic acid group as well as its non-hangman analogue were synthesized and utilized for the study of the proton-coupled electron transfer (PCET) kinetics attendant to electrocatalytic hydrogen evolution. Cyclic voltammetry (CV) together with simulations show that a short distance between the proton relay and the redox active cobalt center as well as the increased proton donating strength results in superior catalytic activity. Here, the mechanism of hydrogen generation is at the nexus of proton transfer–electron transfer (PTET) and concerted proton–electron transfer (CPET), as opposed to an ETPT mechanism that is characteristic of hangman systems with longer proton relay networks.
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
Benchmarking second and third-generation sequencing platforms for microbial metagenomics
Shotgun metagenomic sequencing is a common approach for studying the taxonomic diversity and metabolic potential of complex microbial communities. Current methods primarily use second generation short read sequencing, yet advances in third generation long read technologies provide opportunities to overcome some of the limitations of short read sequencing. Here, we compared seven platforms, encompassing second generation sequencers (Illumina HiSeq 300, MGI DNBSEQ-G400 and DNBSEQ-T7, ThermoFisher Ion GeneStudio S5 and Ion Proton P1) and third generation sequencers (Oxford Nanopore Technologies MinION R9 and Pacific Biosciences Sequel II). We constructed three uneven synthetic microbial communities composed of up to 87 genomic microbial strains DNAs per mock, spanning 29 bacterial and archaeal phyla, and representing the most complex and diverse synthetic communities used for sequencing technology comparisons. Our results demonstrate that third generation sequencing have advantages over second generation platforms in analyzing complex microbial communities, but require careful sequencing library preparation for optimal quantitative metagenomic analysis. Our sequencing data also provides a valuable resource for testing and benchmarking bioinformatics software for metagenomics.
59 BASIC BIOLOGICAL SCIENCES↗
Indirect constraints on third generation baryon number violation
Abstract The non-observation of baryon number violation suggests that the scale of baryon-number violating interactions at zero temperature is comparable to the GUT scale. However, the pertinent measurements involve hadrons made of the first-generation quarks, such as protons and neutrons. One may therefore entertain the idea that new flavour physics breaks baryon number at a much lower scale, but only in the coupling to a third generation quark, leading to observable baryon-number violatingb-hadron decay rates. In this paper we show that indirect constraints on the new physics scale Λ BNV from the existing bounds on the proton lifetime do not allow for this possibility. For this purpose we consider the three dominant proton decay channelsp→$$ {\ell}^{+}{\nu}_{\ell}\overline{\nu} $$ ℓ + ν ℓ ν ¯ ,p→$$ {\pi}^{+}\overline{\nu} $$ π + ν ¯ andp→π 0 ℓ + mediated by a virtual bottom quark.
Physics↗
Design of a PIP-II Era Mu2e Experiment
We propose a design of an upgraded Mu2e experiment for the future Fermilab PIP-II era based on the muon collider front end. The consensus is that such an upgrade should provide a factor of 10 increase in the rate of stopping muons in the experimental target. The current Mu2e design is optimized for 8 kW of protons at 8 GeV. The PIP-II upgrade project is a 250-meter-long CW linac capable of accelerating a 2-mA proton beam to a kinetic energy of 800 MeV (total power 1.6 MW). This would significantly improve the Fermilab proton source to enable next-generation intensity frontier experiments. But using this 800 MeV beam poses challenges to the Mu2E experiment. Bright muon beams generated from sources designed for muon collider and neutrino factory facilities have been shown to generate two orders of magnitude more muons per proton than the current Mu2e production target and solenoid. In contrast to the current Mu2e, the muon collider design has forward-production of muons from the target.
43 PARTICLE ACCELERATORS↗
PPS76: A computerized event mode solar proton forecasting technique
A procedure was developed to generate a computerized time intensity profile of the solar proton intensity expected at the Earth after the occurrence of a significant solar flares on the Sun. A combination of many pieces of independent research and theoretical results are included. A construction of selected experimental and theoretical results from the entire domain of solar terrestrial physics is given.
Smart, D. F.↗
Generation of radioisotopes for medical applications using high-repetition, high-intensity lasers
We used the PW high-repetition laser facility VEGA-3 at Centro de Láseres Pulsados in Salamanca, with the goal of studying the generation of radioisotopes using laser-driven proton beams. Various types of targets have been irradiated, including in particular several targets containing boron to generate α-particles through the hydrogen–boron fusion reaction. We have successfully identified γ-ray lines from several radioisotopes created by irradiation using laser-generated α-particles or protons including 43 Sc, 44 Sc, 48 Sc, 7 Be, 11 C and 18 F. We show that radioisotope generation can be used as a diagnostic tool to evaluate α-particle generation in laser-driven proton–boron fusion experiments. We also show the production of 11 C radioisotopes, ≈ 6 × 10 6 , and of 44 Sc radioisotopes, ≈ 5 × 10 4 per laser shot. This result can open the way to develop laser-driven radiation sources of radioisotopes for medical applications.
gamma ray spectroscopy↗
Search for pair-produced vector-like leptons in final states with third-generation leptons and at least three b quark jets in proton-proton collisions at s = 13 TeV
The first search is presented for vector-like leptons (VLLs) in the context of the “4321 model”, an ultraviolet-complete model with the potential to explain existing B physics measurements that are in tension with standard model predictions. The analyzed data, corresponding to an integrated luminosity of 96.5 fb − 1 , were recorded in 2017 and 2018 with the CMS detector at the LHC in proton-proton collisions at s = 13 TeV . Final states with ≥3 b -tagged jets and two third-generation leptons (ττ, τ ν τ , or ν τ ν τ ) are considered. Upper limits are derived on the VLL production cross section in the VLL mass range 500–1050 GeV. The maximum likelihood fit prefers the presence of signal at the level of 2.8 standard deviations, for a representative VLL mass point of 600 GeV. As a consequence, the observed upper limits are approximately double the expected limits.
72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗
Radiation damage effects in beryllium for next generation neutrino beam targetry (Final Technical Report)
Current and future high-power accelerators put severe requirements on materials used for target and beam windows and target facilities have been recognized as a critical challenge in development of future particle accelerators. In accelerators, window and target materials are exposed to extreme conditions, which include bombardment with very high energy protons (1- 100 GeV) and thermomechanical shock waves. Radiation can cause direct damage in the material, and it leads to production of transmutation products (especially helium), both phenomena having a potential adverse effect on the stability and durability of the target/window material. At high enough temperatures, He can aggregate to form gas bubbles, which in turn cause significant dimensional changes (swelling), enable easy crack propagation, and eventually cause failure by fracture. On the other hand, if the temperature is too low, radiation damage accumulates in the form of internal defects (e.g., dislocations), leading to hardening and a decreased ductility of the material. In this project, we will focus on beryllium since it is considered to be one of the candidate materials for beam windows and targets in the next-generation proton accelerators, e.g., the Long Baseline Neutrino Facility (LBNF). Radiation effects in Be have been studied in the context of nuclear fusion reactor applications. However, key differences exist between reactor and accelerator conditions, including neutron vs. proton irradiation, continuous vs. pulsed beam flux, much higher energies of bombarding particles in accelerators, and higher operating temperatures for typical reactors. For example, the impact of beam pulsing on the radiation damage and the He bubble kinetics is largely unknown. While results obtained on Be from fusion research might not be directly transferrable to understanding target materials, there is an opportunity to bring state-of-the-art tools from materials research in nuclear reactors to aid design of target and beam window materials in high-power accelerators. To this end, the overarching goal of this project are to develop an experimentally-validated computational framework capable of predicting radiation damage evolution in beryllium relevant to beam window and target conditions, focusing on He bubble formation and growth as a function of irradiation temperature. Our model will be based on the cluster dynamics formalism, where size distribution of defects and He bubbles is simulated as a function of time, temperature, and radiation dose. Parameters for the model will be taken from published experiments and from high-fidelity atomistic simulations proposed in this project. In addition, we will carry out a series of targeted ex-situ and in-situ dual-beam experiments using low-energy protons to provide critical data for validation of the model on the effects of radiation on He clustering, He bubble distribution, and dislocation loop density/size in proton irradiated Be.
36 MATERIALS SCIENCE↗
A Platform for Ultra-Fast Proton Probing of Matter in Extreme Conditions
Recent developments in ultrashort and intense laser systems have enabled the generation of short and brilliant proton sources, which are valuable for studying plasmas under extreme conditions in high-energy-density physics. However, developing sensors for the energy selection, focusing, transport, and detection of these sources remains challenging. This work presents a novel and simple design for an isochronous magnetic selector capable of angular and energy selection of proton sources, significantly reducing temporal spread compared to the current state of the art. The isochronous selector separates the beam based on ion energy, making it a potential component in new energy spectrum sensors for ions. Analytical estimations and Monte Carlo simulations validate the proposed configuration. Due to its low temporal spread, this selector is also useful for studying extreme states of matter, such as proton stopping power in warm dense matter, where short plasma stagnation time (<100 ps) is a critical factor. The proposed selector can also be employed at higher proton energies, achieving final time spreads of a few picoseconds. This has important implications for sensing technologies in the study of coherent energy deposition in biology and medical physics.
46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗
Response function generation for transmutation of Technetium-99 via high energy proton and neutron interactions in MCNP
Not Available
Hearne, Jason A. (ORCID:0000000173434182)↗
A unified theory of stable auroral red arc formation at the plasmapause
A theory is proposed that SAR-arcs are generated at the plasmapause as a consequence of the turbulent dissipation of ring current energy. During the recovery phase of a geomagnetic storm, the plasmapause expands outward into the symmetric ring current. When the cold plasma densities reach about 100/cu cm, ring current protons become unstable and generate intense ion cyclotron wave turbulence in a narrow region 1/2 earth radius wide (just inside the plasmapause). Approximately one-half of the ring current energy is dissipated into wave turbulence which in turn is absorbed through a Landau resonant interaction with plasma spheric electrons. The combined thermal heat flux to the ionosphere due to Landau absorption of the wave energy and proton-electron Coulomb dissipation is sufficient to drive SAR-arcs at the observed intensities. It is predicted that the arcs should be localized to a narrow latitudinal range just within the stormtime plasmapause. They should occur at all local times and persist for the 10 to 20 hour duration of the plasma-pause expansion.
Cornwall, J. M.↗
Generating Potent C–H PCET Donors: Ligand-Induced Fe-to-Ring Proton Migration from a Cp*Fe III –H Complex Demonstrates a Promising Strategy
Highly reactive organometallic species that mediate reductive proton-coupled electron transfer (PCET) reactions are an exciting area for development in catalysis, where a key objective focuses on tuning the reactivity of such species. Here, this work pursues ligand-induced activation of a stable organometallic complex toward PCET reactivity. This is studied via the conversion of a prototypical Cp*Fe III –H species, [Fe III (η 5 -Cp*)(dppe)H] + (Cp* = C 5 Me 5 –, dppe = 1,2-bis(diphenylphosphino)ethane), to a highly reactive, S = 1/2 ring-protonated endo-Cp*H–Fe relative, triggered by the addition of CO. Our assignment of the latter ring-protonated species contrasts with its previous reported formulation, which instead assigned it as a hypervalent 19-electron hydride, [Fe III (η 5 -Cp*)(dppe)(CO)H] + . Herein, pulse EPR spectroscopy ( 1,2 H HYSCORE, ENDOR) and X-ray crystallography, with corresponding DFT studies, cement its assignment as the ring-protonated isomer, [Fe I (endo-η 4 -Cp*H)(dppe)(CO)]+. A less sterically shielded and hence more reactive exo-isomer can be generated through oxidation of a stable Fe 0 (exo-η 4 -Cp*H)(dppe)(CO) precursor. Both endo- and exo-ring-protonated isomers are calculated to have an exceptionally low bond dissociation free energy (BDFE C–H ≈ 29 kcal mol –1 and 25 kcal mol –1 , respectively) cf. BDFE Fe–H of 56 kcal mol –1 for [Fe III (η 5 -Cp*)(dppe)H] + . These weak C–H bonds are shown to undergo proton-coupled electron transfer (PCET) to azobenzene to generate diphenylhydrazine and the corresponding closed-shell [Fe II (η 5 -Cp*)(dppe)CO] + byproduct.
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
Electron injection and acceleration at nonlinear shocks: Results of numerical simulations
We present results of numerical simulations of electron injection and acceleration at nonlinear high Mach number shocks. The electrons are assumed to be heated at the thermal subshock to an energy E(sub inj), which is treated as a free parameter, above which they are injected by self-generated whistlers to momentum m(sub p) x V(sub A). This injection mechanism requires Mach numbers greater than (43/(beta(sub -)))(((k T(sub e))/(E(sub inj)))(exp 1/2)), where T(sub e) and beta (sub -) are the upstream electron temperature and plasma beta parameter. Above m(sub p) x V(sub A) electrons are trapped in the shock by Alfven waves. In the proton precursor region the Alfven waves are assumed to be generated by protons accelerated at the shock, and have nonlinear intensities. Below GeV, however, electrons of a given rigidity propagate faster than protons with a similar rigidity and therefore diffuse to regions ahead of the proton precursor. In those regions the Alfven waves are generated by the electrons themselves. The diffusion coefficient appears to increase with decreasing acceleration efficiency. As a result, the number of electrons accelerated to energies GeV and above and, hence, the electron to proton ratio, depend only weakly on the extent of electron heating at the subshock. The negative feedback also renders the electron spectra insensitive to shock compression ratio and smoothing length scale. The estimated e/p ratio at GeV is between approximately 1%-10%.
Levinson, Amir↗
Investigation of the iodate sorption mechanism by CoAl LDH through experiments and ab initio molecular dynamics simulations
Radioiodine released during the nuclear-fuel cycle constitutes a persistent radiological hazard. In this study, the IO 3 – uptake mechanism of CoAl LDH was resolved by combining pH-controlled sorption experiments, synchrotron XAFS, and DFT-based AIMD simulations. At pH close to 6, approximately 90% of IO 3 – was removed, and the equilibrium distribution coefficient reached about 1.7 × 10 4 mL g –1 . EXAFS analysis indicated an average iodine–oxygen bond length of 1.81 Å and a coordination number near 3, with the fit R-factor equal to 0.002. The simulations faithfully reproduced the experimental spectrum and revealed transient proton hopping events that generated metastable I–O–H species inside the interlayer, thereby confirming nitrate-to-iodate exchange as the controlling capture pathway. Atomic density profiles and radial distribution functions further showed that IO 3 – adopt an end-on orientation perpendicular to the hydroxide sheets, while water molecules mediate proton migration without disturbing the host lattice. In conclusion, the integrated experimental–computational evidence demonstrates that CoAl LDH can rapidly and selectively sequester IO 3 – under near-neutral conditions, offering atomic scale guidance for the rational engineering of layered sorbents for advanced radioactive-waste treatment.
Kang, Jaehyuk [Jeju National Univ. (Korea, Republi↗
Laser-assisted high-energy proton pulse extraction for feasibility study of co-located muon source at the SNS
Here, we have experimentally demonstrated the first non-intrusive 1-GeV proton beam extraction for the generation of muons with a temporal structure optimized for Muon Spin Relaxation/Rotation/Resonance (μSR) applications. The proton pulses are extracted based on the laser neutralization of 1 GeV hydrogen ion (H - ) beam in the high energy beam transport of the Spallation Neutron Source (SNS) accelerator. The maximum flux of the extracted proton beam based on laser neutralization causes only 0.2% reduction of the total proton beam used for neutron production, a marked difference from the 20% reduction at other co-located muon and neutron facilities, and thus the proposed method will result in negligible impact on the SNS operation. This paper describes the development of a fiber/solid-state hybrid laser system that has high flexibility of pulse structure and output power, initial experiments on laser neutralization of beam and separation of H 0 beam from the existing SNS accelerator beam line, conversion of H 0 to proton at the SNS linac dump, and measurement results of 30 ns/50 kHz proton pulses. This system conclusively demonstrates the feasibility of laser-based proton beam extraction to power a world-leading μSR facility at the SNS.
46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗
Probing the Sustainable Reduction of CO 2 , N 2 and NO 3 to Fuels and Chemicals using Non-Traditional Porphyrinoid Catalysts
For the last several decades, numerous strategies have been proposed to be able to interconvert electricity and commodity fuels for transportation and other applications. Even as solar and wind energy become more widely available, these renewable energy sources are not always available where the population is most dense or during peak times of energy demand. One plausible solution to the issue of electricity storage and transport is to use electricity to drive the formation of high-energy compounds and chemical fuels. As a result, the electrochemical conversion of CO 2 into chemical fuels has received major attention as a multi-pronged approach for electricity coversion, storage, and transport. Similar strategies are also attractive for conversion of N 2 and NO x into value added compounds such as ammonia. Metalloporphyrin and metallocorrole complexes are comprised of aromatic tetrapyrrole scaffolds and have been extensively studied as homogeneous catalysts for critical catalytic processes like the electrochemical CO 2 reduction reaction (eCO 2 RR) to generate CO as feedstock for the Fischer–Tropsch process to generate a variety of hydrocarbons as chemical fuels. Despite their significance and impact, efficiently driving such catalytic reduction processes is challenging for multiple reasons. Such processes require multiple-electron transfer events, as opposed to single-electron redox chemistry that forms high-energy singly-reduced intermediates. In addition, these electron transfer events must be coupled to proton-transfer steps and avoid application of high overpotentials where proton (H + ) reduction to generate H 2 (as well as other side-reactions) can lower the selectivity and energy efficiency of the eCO 2 RR process. Certain Fe(III) aromatic tetrapyrroles (e.g., porphyrins and corroles) have been reported to overcome these challenges, but are often difficult to synthesize and modify, and have a tendency to support single-electron redox chemistry at the metal as opposed to multielectron redox involving the ligand and metal in concert. Other families of tetrapyrroles in which all four meso-carbons are reduced (i.e., sp 3 -hybridized) are also known in the literature. These non-aromatic tetrapyrroles are known as porphyrinogens and support multi-electron redox chemistry which has been elaborated by several groups, prompting researchers to consider whether these scaffolds may improve the kinetics and efficiencies of multi-electron steps attendant to activation of thermodynamically stable small-molecule substrates such as CO 2 , N 2 , NO 3 − , and NO 2 − . Although porphyrinogens support multi-electron redox properties, the four sp 3 -hybridized meso-carbons inherent to the tetrapyrrole core completely disrupt π-conjugation between pyrrolic units, which compromises the photochemical properties of porphyrinogens in comparison to that of traditional porphyrinoids. Moreover, the highly reducing nature of porphyrinogens predisposes these platforms to extreme air and water sensitivity. Accordingly, such metalated porphyrinogens are often pyrophoric and/or incompatible with many common organic solvents (CH 2 Cl 2 , CHCl 3 , CH 3 CN, EtOAc, etc.). Hence, reports of efficient small-molecule activation or catalysis supported by porphyrinogens have been limited. To overcome the instability of porphyrinogens while retaining the scaffold’s attractive multi-electron redox properties, we have directed attention to establishing less-well studied groups of non-aromatic tetrapyrroles (i.e., phlorins, biladienes, and isocorroles). These non-traditional tetrapyrroles each contain just a single sp 3 -hybridized meso-carbon, which ablates the platforms aromaticity but still provides an extended π-framework. In addition to developing innovative platforms that may be used to sustainably generate value-added chemicals, fuels, and ammonia via either photo- or electrocatalytic approaches our work also has significantly broadened our understanding of how to prepare and modulate the properties of non-aromatic tetrapyrroles for other applications. Our efforts entailed a synergistic partnership and active collaborations with Drs. David C. Grills and Mehmed Z. Ertem (both of Brookhaven National Lab) to better characterize isocorroles (and related non-aromatic tetrapyrroles) using a variety of advanced spectroscopic and theoretical methods. Our combined efforts have shown that the combination of properties that isocorroles (and related tetrapyrroles) provide results in good chemical stability paired with unique redox and photochemical characteristics that are not typically supported by simple and/or unadorned aromatic tetrapyrroles. Beside redox chemistry, the photochemistry of isocorroles and other non-aromatic tetrapyrroles containing one sp 3 -hybridized meso-carbon is also appealing due to their absorption in the long-visible to near-IR regions, which are essential for photocatalysis and related applications that benefit from direct excitation at these wavelengths. The results reported vastly improve our understanding of non-aromatic tetrapyrrole synthesis, properties and utility for activation of small molecule substrates such as O 2 and CO 2 in the presence of weak cationic organic acids.
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗