Nuclear Absorption Research Articles

MAPO-5 molecular sieves from alkylimidazolium bromide ionic liquids

The ionic liquids diisopropylimidazolium bromide (DIPI) and diisobutylimidazolium bromide (DIBU) were used both as solvents and structure-directing agents (SDAs) to obtain AlPO4-5 and MnAPO-5 (Mn-AFI) molecular sieves. For increasing level of manganese, DIBU always yielded pure-phase Mn-AFI whereas DIPI led to amorphous product when more than 0.13 eq of Mn was added. Varying amounts of water, HF and metal led to AFI, cristobalite or tridymite phases. We also explored the use of nickel as the metal dopant, and although AFI phase were obtained under certain conditions, no framework incorporation of the metal was observed. Because of the vanishingly low vapor pressure of the ILs, the synthesis does not carry the risk of pressure build-up. The ILs were easily and fully recyclable and used for multiple syntheses. The MnAPO-5 material was characterized with powder X-ray diffraction (PXRD), thermogravimetric analysis (TGA), electron paramagnetic resonance (EPR), multinuclear solid-state nuclear magnetic resonance (SS-NMR) and X-ray absorption fine structure (XAFS). These findings provide new insight into the ionothermal synthesis of metal-doped AFI frameworks with possible implications in catalytic applications.

Insights about the effect of metal–organic framework hybridization with graphene-like materials

Abstract Hybrids based on the copper-based metal–organic framework HKUST-1 and graphene-like materials (GL) have been synthesized at different concentrations of GL, and investigated by means of solid state nuclear magnetic resonance (ssNMR) and x-ray absorption techniques (NEXAFS and XANES) with the aim of elucidating the effect of the hybridization on the structural properties of HKUST-1. The comparative analysis of ssNMR and x-ray absorption spectra recorded on parent materials (GL and pure HKUST-1) and on the hybrids indicates that the overall structural features of HKUST-1 are preserved in the presence of increasing GL amounts (up to 30 wt.%) and confirms that the framework development is not massively altered by the presence of graphene-related materials (GRMs) in the synthetic medium.

Electronic and Molecular Structures of a Series of Nickel Bis-1,1-Dithiolates.

A series of homoleptic Ni bis-1,1-dithiolates, [Ni(S2C2RR')2]2- (R=CN, R'=CN, CO2Et, CONH2, Ph, Ph-4-Cl, Ph-4-OMe, Ph-4-NO2, Ph-3-CF3, Ph-4-CF3, Ph-4-CN; R=NO2, R'=H; R=R'=CO2Et) have been synthesized from the reaction of the alkali metal salt of the ligand and nickel chloride, and isolated as tetraphenylphosphonium or tetrabutylammonium salts. The complexes were characterized by X-ray crystallography, high-resolution mass spectrometry, and infrared (IR), nuclear magnetic resonance (NMR) and electronic absorption spectroscopies. The molecular structures show a rigidly square planar Ni(II) center linking two four-membered chelate rings whose dimensions are constant across the series. The electronic effect of the ligand substituent is revealed in the 13C NMR and electronic spectra, and corroborated by density functional calculations. Electron withdrawing groups deshield the low-field CS2 resonance, and the signature charge transfer band in the visible region is red-shifted. These observables have been accurately reproduced computationally, and revealed the Ni contribution to the ground state diminishes with decreasing electron withdrawing capacity of the ligand substituent. In contrast to 1,2-dithiolates, the redox inactivity afforded by 1,1-dithiolates stems from the smaller chelate ring and substantially reduced sulfur content that is key to stabilizing the radical form.

Corrosion resistance of aluminum against acid activation in 1.0 M HCl by symmetrical ball − type zinc phthalocyanine

The inhibition effect of symmetrical Ball − type Zinc Phthalocyanine on Aluminum in 1mol/L hydrochloric acid was analyzed by electrochemical techniques. A novel ball-type zinc phthalocyanine (Zn-Pc) inhibitor has been synthesized and verified utilizing FTIR, nuclear magnetic resonance (1H NMR and 13C NMR), MALDI-TOF MS, and absorption spectroscopy (UV-Vis). In addition, laser-induced breakdown and photoluminescence spectroscopy were employed for additional study. Weight loss technique was employed to investigate the corrosion inhibition effectiveness of the synthesized Zn-Pc on Aluminum in 1mol/L hydrochloric acid at the range of variation temperatures (293–333 K). The inhibition efficiency of Zn-Pc increased with higher concentrations of Zn-Pc and decreased as the temperature increased. Furthermore, Zn-Pc demonstrated outstanding outcomes, achieving 72.9% at a very low inhibitor concentration (0.4 mmol/L) at 298 K. The experimental data for Zn-Pc Aluminum in 1mol/L hydrochloric acid obeys the Langmuir adsorption isotherm. Moreover, the corrosion system’s thermodynamic parameters and activation energy were determined. Quantum chemical calculations applying the (DFT) Density Functional Theory method was conducted and applied in this study. These calculations played a pivotal role in elucidating molecular structures and reactivity patterns. Through DFT, numerous reactivity indicators were computed, providing valuable insights into the chemical behavior of the studied compounds. These indicators, such as frontier molecular orbitals, electron density, and molecular electrostatic potential, were subsequently correlated with experimental data.

A novel means to generate high pressure.

Diamond anvil cells are the most popular means of generating pressures above 2GPa. However, in many experiments, such as nuclear magnetic resonance and x-ray absorption, the metallic pressurizing gasket (which confines much of the sample) represents an occluding barrier that requires a low Z gasket material (e.g., Be), a split gasket, or other means to enable better coupling of the sample to electromagnetic radiation. In this paper, we demonstrate a novel method for generating high pressures that confines the sample just above the plane of the gasket by using a diamond with a laser hole drilled into the center of the tip. The sample is then confined by the hole, which is sealed by a flat gasket that fits over the hole. When load is applied to the diamonds, metal flows from the deformed gasket into the hole thereby pressurizing the sample similarly to how a piston pressurizes gas inside a cylinder. The pressurized sample is above the metallic gasket plane just inside the tip of the diamond, and thus easily accessible via x rays or visible light that skims just above the plane of the gasket providing an enhanced aperture of radiation collection. We have demonstrated the utility of this method by obtaining Raman spectra of SnC2O4 and x-ray diffraction spectra of seleno-DL-cystine, all at high pressures.

Nuclear quantum memory for hard x-ray photon wave packets.

Optical quantum memories are key elements in modern quantum technologies to reliably store and retrieve quantum information. At present, they are conceptually limited to the optical wavelength regime. Recent advancements in x-ray quantum optics render an extension of optical quantum memory protocols to ultrashort wavelengths possible, thereby establishing quantum photonics at x-ray energies. Here, we introduce an x-ray quantum memory protocol that utilizes mechanically driven nuclear resonant 57Fe absorbers to form a comb structure in the nuclear absorption spectrum by using the Doppler effect. This room-temperature nuclear frequency comb enables us to control the waveform of x-ray photon wave packets to a high level of accuracy and fidelity using solely mechanical motions. This tunable, robust, and highly flexible system offers a versatile platform for a compact solid-state quantum memory at room temperature for hard x-rays.

Application of Energy‐Resolving Neutron Imaging to Major‐Component Analyses of Materials Using Four‐Channel Superconducting Detector

We proposed a current‐biased kinetic inductance detector (CB‐KID) as a novel superconducting detector to construct a neutron transmission imager. The characteristics of a superconducting neutron detector have been systematically studied to improve a spatial resolution down to 10 in transmission imaging. In this study, we report the application of the energy‐resolving neutron imaging to investigate major components of materials by analyzing neutron transmission spectra from 1 meV to 500 keV. We succeeded in identifying that copper (Cu) and iron (Fe) are major components respectively in commercial nuts and screws as test samples with the aid of Rietveld imaging of transmission spectra (RITS) program in analyzing transmission spectra in longer wavelengths. The Ti screw was also confirmed by comparing the nuclear resonance absorption measurements and simulations in high‐energy regions. We demonstrated that our superconducting neutron detector is applicable to reveal the transmission spectra in the wide range from cold‐neutron energies to higher neutron energies even up to 500 keV. By selecting distinctive energy regions of pulsed neutrons, we succeeded in mapping the distribution of SmSn3 compound using the strong neutron absorption in samarium (Sm) and the selective nuclear‐resonance dips in Sm. By taking advantage of using CB‐KID in conducting neutron imaging, the CB‐KID method is extensively useful for various purposes in material sciences through energy‐selective neutron spectroscopy from 1 meV to 500 keV. © 2024 Institute of Electrical Engineers of Japan and Wiley Periodicals LLC.

Nucleon-nucleon correlations probed in sub-barrier transfer reactions and the nuclear Josephson effect

In recent years a series of near- and sub-barrier transfer experiments have been carried out at LNL, with reaction products detected in inverse kinematics and at forward angles with the large solid angle magnetic spectrometer PRISMA. Nucleon-nucleon correlation properties have been studied by measuring transfer cross sections far below the Coulomb barrier, making excitation functions down to very low energies and corresponding to very large distances of closest approach where the nuclear absorption is small. Such kind of studies are of general interest since one probes the tails of the density distributions. One subtle case is the possible manifestation of a nuclear Josephson effect. Predictions have been made of a specific gamma strength function associated with the dipole oscillations generated by the, mainly successive, two neutron transfer process. The coupling of PRISMA to the AGATA gamma array, recently installed at LNL, offered a unique opportunity to study such an effect. In a very recent experiment we directly tested for the first time the possible manifestation of Cooper pair oscillations, observed to date only in condensed matter physics.

The measurement of the E2 nuclear resonance effects in kaonic atoms at DAΦNE: The KAMEO proposal

KAMEO (Kaonic Atoms Measuring Nuclear Resonance Effects Ob-servables) is a proposal for an experiment aiming to perform the first consistent measurement of the E2 nuclear resonance effects in kaonic molybdenum A=94,96,98,100 isotopes. The E2 nuclear resonance mixes atomic states, due to the electrical quadrupole excitation of nuclear rotational states. It occurs in atoms having the energy of a nuclear excitation state closely matching an atomic de-excitation state energy, and affects the rates of X-ray atomic transitions matching the energy of the resonance. The measurement E2 nuclear resonance effect in KMO isotopes allows the study of the strong kaon-nucleus interaction in a rotational excited nuclear state. Moreover, the effect enables the K- to access an inner atomic level not easily reachable by the kaon normal cascade, due to the nuclear absorption. The KAMEO proposed apparatus consists of 4 enriched Mo A=94,96,98,100 isotope strips, exposed to the kaons produced by the DAφNE collider, for kaonic atoms formation, with a high-purity germanium detector, cooled with liquid nitrogen, used to measure the X-ray atomic transitions. The DAφNE collider is located at the National Laboratories of Frascati (LNF-INFN), in Italy. It is already suited for kaonic atoms measurement by the SIDDHARTA-2 collaboration.

Recent progress of in-situ/operando characterization approaches of zinc-air batteries

Zinc-air batteries (ZABs) belong to the category of metal-air batteries, with high theoretical energy density, safety, and low cost. Nevertheless, there are still many challenges that need to be solved for the practical application of ZABs, including high overpotential, poor cycle life, and so on. This article first briefly introduced the principle of ZABs, covering the key components, functions of each element, and challenges faced by the system. Subsequently, seven methods for studying ZABs in-situ or operando were introduced, including X-ray computed tomography (XCT), optical microscopy imaging (OMI), transmission electron microscopy, nuclear magnetic resonance imaging (MRI), X-ray diffraction (XRD), Raman spectroscopy, and X-ray absorption spectroscopy, accompanied by specific research examples. The future perspectives of ZAB characterization have also been discussed.

Achieving narrow bandwidth and high stimulated cross-section in Nd3+-doped LiCaB glasses for near infra-red laser amplifiers

The aim of this research is to examine the effects of Nd3+ ions on the spectroscopic characteristics of different concentrations of lithium-calcium-borate glasses and improve the emission cross section alongside bandwidth. The prepared glasses were produced with the melt-quenching technique and were thoroughly analyzed to determine their usefulness as laser amplifiers. Various studies were conducted, including X-ray diffraction (XRD), solid-state nuclear magnetic resonance (NMR), thermogravimetric analysis (TGA), absorption and emission measurements, and time decay curve measurements. The structural analysis using XRD and NMR techniques revealed that the glasses were amorphous and that non-bridging oxygen was present. Moreover, it was discovered that the glass-forming tendency and glass stability of these glasses improved with the concentration of Nd3+ ions. The glasses' absorption spectra display 10 transition states in UV and visible regions. Among all the prepared glasses, the lithium-calcium-borate glass doped with 0.5 mol % Nd3+ ions stand out with a stimulated emission cross-section value of 3.40 × 10−20 cm2 and a narrow bandwidth of 33 nm, making it an ideal lasing amplifier medium due to the 4F3/2 → 4I11/2 (1060 nm) transition. Theoretical Judd-Ofelt calculations were conducted to evaluate various parameters, including oscillatory strength, radiative parameters, radiative lifetime, gain bandwidth, figure-of-merit, and saturation current, for all transitions in the near-infrared region, to support the experimental investigations and offer a detailed discussion of these parameters.

The Galaxy Activity, Torus, and Outflow Survey (GATOS)

We use JWST/MIRI MRS spectroscopy of a sample of six local obscured type 1.9/2 active galactic nuclei (AGN) to compare their nuclear mid-IR absorption bands with the level of nuclear obscuration traced by X-rays. This study is the first to use subarcsecond angular resolution data of local obscured AGN to investigate the nuclear mid-IR absorption bands with a wide wavelength coverage (4.9–28.1 μm). All the nuclei show the 9.7 μm silicate band in absorption. We compare the strength of the 9.7 and 18 μm silicate features with torus model predictions. The observed silicate features are generally well explained by clumpy and smooth torus models. We report the detection of the 6 μm dirty water ice band (i.e., a mix of water and other molecules such as CO and CO2) at subarcsecond scales (∼0.26″ at 6 μm; inner ∼50 pc) in a sample of local AGN with different levels of nuclear obscuration in the range log NHX-Ray (cm−2)∼22 − 25. We find good correlation between the 6 μm water ice optical depths and NHX-Ray. This result indicates that the water ice absorption might be a reliable tracer of the nuclear intrinsic obscuration in AGN. The weak water ice absorption in less obscured AGN (log NHX-ray (cm−2)≲23.0 cm−2) might be related to the hotter dust temperature (> TsubH2O ∼ 110 K) expected to be reached in the outer layers of the torus due to their more inhomogeneous medium. Our results suggest it might be necessary to include the molecular content, such as H2O, aliphatic hydrocarbons (CH−), and more complex polycyclic aromatic hydrocarbon (PAH) molecules, in torus models to better constrain key parameters such as the torus covering factor (i.e., nuclear obscuration).

Systematic Analysis of the Nuclear Absorption Effect on the Cross Section of the Knockout Reaction

Systematic Analysis of the Nuclear Absorption Effect on the Cross Section of the Knockout Reaction

A review of the low-energy K−-nucleus/nuclei interactions with light nuclei AMADEUS investigations

The AMADEUS Collaboration conducts research aimed to experimentally investigate the low-energy K− hadronic interactions with light nuclei like hydrogen, helium, and carbon, in order to provide new constraints to the antikaon-nucleon strong interaction studies in the non-perturbative quantum chromodynamics regime. K− nuclear absorption, both at-rest and in-flight, are explored using the unique low-momentum and monochromatic kaon beam from the DAΦNE collider interacting with the KLOE detector components, a detector characterized by high acceptance and excellent position and momentum resolutions. This paper presents an overview of the AMADEUS results.

Orientation mapping of YbSn3 single crystals based on Bragg-dip analysis using a delay-line superconducting sensor

Recent progress in high-power pulsed neutron sources has stimulated the development of the Bragg-dip and Bragg-edge analysis methods using a two-dimensional neutron detector with high temporal resolution to resolve the neutron energy by the time-of-flight method. A delay-line current-biased kinetic inductance detector (CB-KID) is a two-dimensional superconducting sensor with a high temporal resolution and multi-hit capability. Here, it is demonstrated that a delay-line CB-KID with a 10B neutron conversion layer can be applied to high-spatial-resolution neutron transmission imaging and spectroscopy up to 100 eV. Dip structures are observed in the transmission spectra of YbSn3 single crystals, induced by Bragg diffraction and nuclear resonance absorption. The orientation mapping of YbSn3 crystals is successfully performed via the analysis of observed Bragg-dip positions in the transmission spectra.

Crystalline Orientation of CaF2 window determined by Neutron Transmission Imaging using a Delay Line Current-Biased Kinetic-Inductance Detector

The combination of a high speed two-dimensional neutron detector and an intensive pulsed neutron source provides not only neutron transmission imaging but also information on crystal structures, orientations and constituent elements by analyzing neutron transmission spectra. The delay-line current-biased kinetic-inductance detector (CB-KID) is a two-dimensional superconducting neutron detector with high spatial and temporal resolutions, and multi-hit tolerance. We demonstrated that the delay-line CB-KID with a 10B neutron conversion layer can be applied for neutron transmission measurements up to 100 keV. We observed two-different dip structures in the transmission spectra in a CaF2 single crystal, i.e., one is from the Bragg diffraction and the other is from nuclear resonance absorption. We consider that some duplicated structures in resonance absorption dips are originating from a double-bunch structure of proton pulses for producing pulsed neutrons in the accelerator.

MOSSBAUER STUDIES OF NATURAL MINERAL RAW MATERIALS OF KAZAKHSTAN FOR BAUXITE-BASED PROPPANTS

The main problem at the oil and gas field is hard-to-recover reserves. The article discusses promising modern methods of increasing oil recovery. The analysis of widely used methods of extraction of hard-to-recover oil and gas reserves is carried out. The Mossbauer studies of the domestic natural mineral raw materials of proppants based on bauxite and aluminum oxides were carried out in order to study the structural and phase features of these materials. Proppants used in hydraulic fracturing to hold cracks play an important role in the oil and gas industry. The Moessbauer method is a powerful tool for studying the structure and electronic state of atoms in materials. It is based on the phenomenon of nuclear gamma resonance absorption and provides information about the chemical environment of the nucleus. In this study, proppants based on bauxite and aluminum oxides were used, which were subjected to a Mossbauer analysis.

Folding of Staphylococcal Nuclease Induced by Binding of Chemically Modified Substrate Analogues Sheds Light on Mechanisms of Coupled Folding/Binding Reactions.

Several proteins have been shown to undergo a shift in the mechanism of ligand binding-induced folding from conformational selection (CS; folding precedes binding) to induced fit (IF; binding precedes folding) with increasing ligand concentration. In previous studies of the coupled folding/binding reaction of staphylococcal nuclease (SNase) in the presence of a substrate analogue, adenosine-3',5'-diphosphate (prAp), we found that the two phosphate groups make important energetic contributions toward stabilizing its complex with the native protein as well as transient conformational states encountered at high ligand concentrations favoring IF. However, the structural contributions of each phosphate group during the reaction remain unclear. To address this question, we relied on fluorescence, nuclear magnetic resonance (NMR), absorption, and isothermal titration calorimetry to study the effects of deletion of the phosphate groups of prAp on the kinetics of ligand-induced folding, using a strategy analogous to mutational ϕ-value analysis to interpret the results. Kinetic measurements over a wide range of ligand concentrations, together with structural characterization of a transient protein-ligand encounter complex using 2D NMR, indicated that, at high ligand concentrations favoring IF, (i) the 5'-phosphate group interacts weakly with denatured SNase during early stages of the reaction, resulting in loose docking of the two domains of SNase, and (ii) the 3'-phosphate group engages in some specific contacts with the polypeptide in the transition state prior to formation of the native SNase-prAp complex.

FeCoNiMnCr high-entropy alloys (HEAs): Synthesis, structural, magnetic and nuclear radiation absorption properties

We report the synthesis and structural, magnetic and Radiation shielding properties of High Entropy Alloy (HEA) produced through mechanical alloying method. Using an X-Ray Diffractometer (PanalyticalEmpryan) with CuK radiation at 45 kV and 40 mA, the phase identification starting elements and as-milled powders are identified. Scanning electron microscopy (SEM) equipped with energy dispersive X-ray spectroscopy (EDX), morphological and microstructural investigations were conducted (FEI Quanta FEG 450). EDX and elemental mapping analyses are conducted to assess the purity and elemental distributions of the synthesized alloys. Using the Quantum Design Physical Characteristics Measurement System (PPMS) with vibrating sample magnetometer (VSM) and a magnetic field of 30 kOe at room temperature, magnetic properties are examined. Using 137Cs radioisotope and mathematical methods, gamma-ray and neutron shielding properties of HEA are investigated in a conventional transmission setup using experimental and theoretical approaches. In the presence of a 3 T applied field, the sample exhibits a low magnetization of 5.30 emu/g at 300 K. Moreover, Ms is raised to 22 emu/g at 10 K owing to decreased thermal effects. The temperature dependence of the magnetization is recorded in the presence of a 1 T applied field. HEA exhibits superior neutron attenuation properties than conventional absorption materials such as B4C, graphite, and water. Our results showed that the synthesized HEA has superiority over other alloys and conventional neutron absorption materials. It can be concluded that the proposed novel HEA might be investigated further in terms of broadening its characterization and clarifying its other crucial properties to extend the scope of the current investigation.

Synthesis and Characterization of Schiff Base Ligands and Their Palladium(II) Complexes

Abstract: This paper is concerned with the preparation and characterization of Schiff base ligands derived from the condensation of salicylaldehyde with three different diamines, namely, ethylenediamine, o-phenylenediamine, and trans-1,2-diaminocyclohexane. The Schiff base ligands were characterized by elemental analysis, melting point, FTIR, UV-Vis, 1H-NMR and 13C-NMR. The Schiff base ligands are reacted with palladium(II) ion via direct reaction or using a template method. Identical complexes were obtained from the two methods with the same percentage yields. The formulas obtained for the complexes are PdC16H16N2O2Cl2, [PdL1]Cl2; PdC16H16N2O2Br2, [PdL1]Br2; PdC16H16N2O2.(BF4)2, [PdL1](BF4)2; PdC20H16N2O2Cl2, [PdL2Cl]Cl; PdC20H16N2O2Br2, [PdL2]Br2; PdC20H15N2O2.BF4, [PdL2]BF4; PdC20H22N2O2Cl2, [PdL3]Cl2; PdC20H22N2O2Br2, [PdL3]Br2; PdC20H20N2O2.2H2O, [PdL3].2H2O. The isolated compounds were characterized based on their melting points, elemental analyses, conductivity measurements, nuclear magnetic resonance, FTIR and electronic absorption spectra.