Small-angle Neutron Scattering Research Articles

SCOMAP-XD: atomistic deuterium contrast matching for small-angle neutron scattering in biology.

The contrast-variation method in small-angle neutron scattering (SANS) is a uniquely powerful technique for determining the structure of individual components in biomolecular systems containing regions of different neutron scattering length density ρ. By altering the ρ of the target solute and the solvent through judicious incorporation of deuterium, the scattering of desired solute features can be highlighted. Most contrast-variation methods focus on highlighting specific bulk solute elements, but not on how the scattering at specific scattering vectors q, which are associated with specific structural distances, changes with contrast. Indeed, many systems exhibit q-dependent contrast effects. Here, a method is presented for calculating both bulk contrast-match points and q-dependent contrast using 3D models with explicit solute and solvent atoms and SASSENA, an explicit-atom SANS calculator. The method calculates the bulk contrast-match points within 2.4% solvent D2O accuracy for test protein-nucleic acid and lipid nanodisc systems. The method incorporates a general model for the incorporation of deuterium at non-exchangeable sites that was derived by performing mass spectrometry on green fluorescent protein. The method also decomposes the scattering profile into its component parts and identifies structural features that change with contrast. The method is readily applicable to a variety of systems, will expand the understanding of q-dependent contrast matching and will aid in the optimization of next-generation neutron scattering experiments.

Effect of yttrium doping in tungsten on sinterability and properties as a plasma-facing material

Y2O3 is extensively used to fabricate oxide-dispersion-strengthened tungsten to refine grain size, improve thermal stability, and increase high-temperature strength. However, excessive Y2O3 addition weakens the grain-boundary strength, which increases the ductile-to-brittle transition temperature. Therefore, in this study, a small amount of Y-rich precipitates was dispersed in a tungsten matrix through internal oxidation during spark plasma sintering. The phase, morphology, and size of the Y-rich precipitates in the sintered tungsten were characterized by transmission electron microscopy (TEM) and small-angle neutron scattering (SANS) analyses. Additionally, the effects of Y doping on sinterability, thermal stability, deuterium irradiation resistance, and mechanical properties were analyzed using Y-free pure tungsten specimens for comparison.

Synergistic Role of Temperature and Salinity in Aggregation of Nonionic Surfactant-Coated Silica Nanoparticles.

The adsorption of nonionic surfactants onto hydrophilic nanoparticles (NPs) is anticipated to increase their stability in aqueous medium. While nonionic surfactants show salinity- and temperature-dependent bulk phase behavior in water, the effects of these two solvent parameters on surfactant adsorption and self-assembly onto NPs are poorly understood. In this study, we combine adsorption isotherms, dispersion transmittance, and small-angle neutron scattering (SANS) to investigate the effects of salinity and temperature on the adsorption of pentaethylene glycol monododecyl ether (C12E5) surfactant on silica NPs. We find an increase in the amount of surfactant adsorbed onto the NPs with increasing temperature and salinity. Based on SANS measurements and corresponding analysis using computational reverse-engineering analysis of scattering experiments (CREASE), we show that the increase in salinity and temperature results in the aggregation of silica NPs. We further demonstrate the non-monotonic changes in viscosity for the C12E5-silica NP mixture with increasing temperature and salinity and correlate the observations to the aggregated state of NPs. The study provides a fundamental understanding of the configuration and phase transition of the surfactant-coated NPs and presents a strategy to manipulate the viscosity of such dispersion using temperature as a stimulus.

Unusual phosphatidylcholine lipid phase behavior in the ionic liquid ethylammonium nitrate

HypothesisThe forces that govern lipid self-assembly ionic liquids are similar to water, but their different balance can result in unexpected behaviour. ExperimentsThe self-assembly behaviour and phase equilibria of two phospholipids, 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC) and 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC), in the most common protic ionic liquid, ethylammonium nitrate (EAN) have been investigated as function of composition and temperature by small- and wide-angle X-ray scattering (SAXS/WAXS) and small-angle neutron scattering (SANS). FindingsBoth lipids form unusual self-assembly structures and show complex and unexpected phase behaviour unlike that seen in water; DSPC undergoes a gel Lβ to crystalline Lc phase transition on warming, while POPC forms worm-like micelles L1 upon dilution. This surprising phase behaviour is attributed to the large size of the EAN ions that solvate the lipid headgroup compared to water changing amphiphile packing. Weaker H-bonding between EAN and lipid headgroups also contributes. These results provide new insight for the design of lipid based nanostructured materials in ionic liquids with atypical properties.

Structural Changes in Liposomal Vesicles in Association with Sodium Taurodeoxycholate.

Liposomes composed of soy lecithin (SL) have been studied widely for drug delivery applications. The stability and elasticity of liposomal vesicles are improved by incorporating additives, including edge activators. In this study, we report the effect of sodium taurodeoxycholate (STDC, a bile salt) upon the microstructural characteristics of SL vesicles. Liposomes, prepared by the thin film hydration method, were characterized by dynamic light scattering (DLS), small-angle neutron scattering (SANS), electron microscopy, and rheological techniques. We noticed a reduction in the size of vesicles with the incremental addition of STDC. Initial changes in the size of spherical vesicles were ascribed to the edge-activating action of STDC (0.05 to 0.17µM). At higher concentrations (0.23 to 0.27µM), these vesicles transformed into cylindrical structures. Morphological transitions at higher STDC concentrations would have occurred due to its hydrophobic interaction with SL molecules in the bilayer. This was ascertained from nuclear magnetic resonance observations. Whereas shape transitions underscored the deformability of vesicles in the presence of STDC, the consistency of bilayer thickness ruled out any dissociative effect. It was interesting to notice that SL-STDC mixed structures could survive high thermal stress, electrolyte addition, and dilution.

Advanced polarization analysis capability on the very small-angle neutron scattering instrument at the NIST Center for Neutron Research

The Very Small Angle Neutron Scattering (VSANS) diffractometer at the National Institute of Standards and Technology has been commissioned and is in the user program. A large available space of nearly 2 m along the beam in the sample area not only enhances the existing SANS polarization analysis capability, but also makes it possible for implementation of other polarization analysis capabilities which would not be easily available on existing SANS instruments, including grazing-incidence small-angle neutron scattering with polarization analysis and spherical neutron polarimetry. We present two polarized setups, one for high magnetic sample fields and the other for low magnetic sample fields, together with a versatile and flexible operational platform for polarized beam experiments. The design of a magnetostatic cavity device that provides better field homogeneity and thus longer 3He polarization relaxation time is discussed. It consists of an end-compensated magnetic shielded solenoid with non-identical holes to accommodate the divergent scattered beam in a constrained distance. Significant improvement in polarized neutronic performance, 3He polarization relaxation time, and an extended momentum transfer range for polarization analysis are presented. Improved neutron polarizing devices, double V-shaped supermirror polarizer, adiabatic radio-frequency spin flipper, and a 3He spin analyzer have yielded an initial instrumental flipping ratio of 100, allowing for higher sensitivity to detection of weak magnetic features in the sample.

Cholesterol and Melatonin Exert Opposite Effects on the Interaction of Model DMPC Membranes with the SARS‐CoV‐2 S‐Protein: A SANS Study

AbstractAn effect of receptor‐binding domain (RBD) of SARS‐CoV‐2 S‐protein on structural parameters of model lipid membranes presented by dimyristoylphosphatidylcholine (DMPC) systems with cholesterol and melatonin impurities is studied by small angle neutron scattering (SANS). It is shown that an increase in melatonin concentration in the lipid membrane leads to a decrease in the thickness of the lipid bilayer, while an increase in the concentration of cholesterol leads to an increase in its thickness. It is suggested that increasing the concentration of melatonin in a membrane prevents the interaction of coronaviral S‐protein with a lipid membrane of a cell. In the presence of cholesterol in the system, the interaction of a lipid membrane with an active part of S‐protein occurs depending on a phase state of the lipid: in the case of a gel phase, there is no changes in structural parameters, but at higher temperatures in the case of a liquid crystal phase, an addition of RBD SARS‐CoV‐2 to the system causes a reduce in the membrane thickness.

Revealing magnetic correlations in ferromagnetic alloys with polarized SANS

We search for magnetic correlations at the nanoscale in a ferromagnetic alloy with low critical temperature Tc and reduced magnetic moments. We present a small-angle neutron scattering (SANS) study of the binary alloy Ni0.89 V0.11 close to the quantum critical point where the ferromagnetic order is destroyed towards a paramagnetic phase by sufficient V concentration. We demonstrate the challenge and the advantage of a fully polarized SANS analysis to discriminate the small magnetic components from the dominant nuclear contributions. We focus on the azimuthal angle dependence of selected cross sections, like pure spin-flip and non spin-flip asymmetry, to finally reveal magnetic contributions at different length scales.

Nanoscale Structure of Positive Electrodes for Lithium-Ion Batteries with Graphene-Based Additives According to Small-Angle Neutron Scattering

Nanoscale Structure of Positive Electrodes for Lithium-Ion Batteries with Graphene-Based Additives According to Small-Angle Neutron Scattering

Conceptual Polarization Setup at CENTAUR, the SANS/WANS Instrument at the Second Target Station of SNS

CENTAUR is a multifunctional general purpose small-angle and wide-angle neutron scattering instrument with diffraction and spectroscopic capability in the future Second Target Station at the Spallation Neutron Source of the Oak Ridge National Laboratory. To fill a gap in neutron polarization capability, the instrument will be designed to provide polarization analysis. Here we present the conceptual polarization setup at CENTAUR, as well as the Spin Echo Modulated Small-Angle Neutron Scattering setup which will further expand the length scale covered by the instrument.

Nanoscale Structure of Positive Electrodes for Lithium-Ion Batteries with Graphene-Based Additives according to Small-Angle Neutron Scattering

Nanoscale Structure of Positive Electrodes for Lithium-Ion Batteries with Graphene-Based Additives according to Small-Angle Neutron Scattering

Combining branched copolymers with additives generates stable thermoresponsive emulsions with in situ gelation upon exposure to body temperature

Branched copolymer surfactants (BCS) containing thermoresponsive polymer components, hydrophilic components, and hydrophobic termini allow the formation of emulsions which switch from liquid at room temperature to a gel state upon heating. These materials have great potential as in situ gel-forming dosage forms for administration to external and internal body sites, where the emulsion system also allows effective solubilisation of a range of drugs with different chemistries. These systems have been reported previously, however there are many challenges to translation into pharmaceutical excipients. To transition towards this application, this manuscript describes the evaluation of a range of pharmaceutically-relevant oils in the BCS system as well as evaluation of surfactants and polymeric/oligomeric additives to enhance stability. Key endpoints for this study are macroscopic stability of the emulsions and rheological response to temperature. The effect of an optimal additive (methylcellulose) on the nanoscale processes occurring in the BCS-stabilised emulsions is probed by small-angle neutron scattering (SANS) to better comprehend the system. Overall, the study reports an optimal BCS/methylcellulose system exhibiting sol–gel transition at a physiologically-relevant temperature without macroscopic evidence of instability as an in situ gelling dosage form.

Quantifying the kinetics of δʹ precipitates in a novel Al–Li–Cu–Mg alloy during two-step aging by small-angle neutron scattering

The kinetics of Li-rich clustering in multicomponent Al–Li–Cu–Mg is not only critical for manufacturing high-strength and modulus products but also important for designing better alloying chemistry. In this study, the ordering of δʹ (Al3Li) has been quantified as a function of temperature and time in a multicomponent Al-10.3Li-0.6Cu-1.4 Mg (at.%) using Transmission Electron Microscope (TEM) and Small-Angle Neutron Scattering (SANS). By measuring the δʹ radius and volume fraction using SANS, it has been found that the precipitation kinetics of δʹ phase at 175 °C can be well described by Lifshitz-Slyozov-Wagner (LSW) theory due to the size of δʹ phase stabilized by the pre-aging at 120°C-4h. The 1.5% pre-strain before solution heat treatment accelerates the δʹ precipitation kinetics and increases its volume fraction by providing more decomposition sites for the δʹ phase and fast diffusing paths for Li atoms. Interestingly, a dissolution behavior of δʹ has been found at the beginning of the second step of aging. This is further confirmed by HRTEM and Monte Carlo simulations, which are associated with the transition from ordering to disordering between the δʹ and the surrounding solid solution. Finally, the strengthening effects of δʹ are quantified and the strength of aged alloys has been found to largely correlate with the δʹ radius while the elastic modulus is more dependent on δʹ volume fraction.

Sequence-Enhanced Self-Healing in "Lock-and-Key" Copolymers.

Van der Waals-driven self-healing in copolymers with "lock-and-key" architecture has emerged as a concept to endow engineering-type polymers with the capacity to recover from structural damage. Complicating the realization of "lock-and-key"-enabled self-healing is the tendency of copolymers to form nonuniform sequence distributions during polymerization reactions. This limits favorable site interactions and renders the evaluation of van der Waals-driven healing difficult. Here, methods for the synthesis of lock-and-key copolymers with prescribed sequence were used to overcome this limitation and enable the deliberate synthesis of "lock-and-key" architectures most conducive to self-healing. The effect of molecular sequence on the material's recovery behavior was evaluated for the particular case of three poly(n-butyl acrylate/methyl methacrylate) [P(BA/MMA)] copolymers with similar molecular weights, dispersity, and overall composition but with different sequences: alternating (alt), statistical (stat), and gradient (grad). They were synthesized using atom transfer radical polymerization (ATRP). Copolymers with alt and stat sequence displayed a 10-fold increase of recovery rate compared to the grad copolymer variant despite a similar overall glass transition temperature. Investigation with small-angle neutron scattering (SANS) revealed that rapid property recovery is contingent on a uniform microstructure of copolymers in the solid state, thus avoiding the pinning of chains in glassy MMA-rich cluster regions. The results delineate strategies for the deliberate design and synthesis of engineering polymers that combine structural and thermal stability with the ability to recover from structural damage.

Enabling Efficient Design of Biological Formulations Through Advanced Characterization.

The present review summarizes the use of differential scanning calorimetry (DSC) and scattering techniques in the context of protein formulation design and characterization. The scattering techniques include wide angle X-ray diffractometry (XRD), small-angle neutron scattering (SANS) and small-angle X-ray scattering (SAXS). While DSC is valuable for understanding thermal behavior of the excipients, XRD provides critical information about physical state of solutes during freezing, annealing and in the final lyophile. However, as these techniques lack the sensitivity to detect biomolecule-related transitions, complementary characterization techniques such as small-angle scattering can provide valuable insights.

Thermodynamics and Phase Behavior of Poly(ethylene oxide)/Poly(methyl methacrylate)/Salt Blend Electrolytes Studied by Small-Angle Neutron Scattering

Thermodynamics and Phase Behavior of Poly(ethylene oxide)/Poly(methyl methacrylate)/Salt Blend Electrolytes Studied by Small-Angle Neutron Scattering

Investigation of Nanostructure and Interactions in Water-in-Xylene Microemulsions Using Small-Angle X-ray and Neutron Scattering.

The ability to modulate the size, the nanostructure, and the macroscopic properties of water-in-oil microemulsions is useful for a variety of technological scenarios. To date, diverse structures of water-in-alkane microemulsions stabilized by sodium bis(2-ethylhexyl) sulfosuccinate (AOT) have been extensively studied. Even though the decisive parameter which dictates the phase behavior of micremulsions is the nature of the continuous phase, relatively very few reports are available on the structure and interactions in the microemulsions of aromatic oil. Here, we present a fundamental investigation on water-in-xylene microemulsions using small-angle neutron scattering (SANS) at a fixed molar ratio (ω) of water to AOT. We elucidate the microstructural changes in the water-AOT-xylene ternary system at dilute volume fractions (Φ = 0.005, 0.01, 0.03), where the droplet-droplet interactions are absent, to moderately concentrated systems (Φ = 0.05, 0.10, 0.15, and 0.20), where colloidal interactions become important. We also characterize the reverse microemulsions (RMs) for thermally induced microstructural changes at six different temperatures from 20 to 50 °C. Depending on the magnitude of Φ, the scattering data is found to be well described by considering the RMs as a dispersion of droplets (with a Schulz polydispersity) which interact as sticky hard spheres. We show that while the droplet diameter remains almost constant with increase in the volume fraction, the attractive interactions become prominent, much like the trends observed for water-in-alkane microemulsions. With increase in temperature, the RMs showed a marginal decrease in the droplet size but no pronounced dependence on the interactions was observed with the overall structure remaining intact. The fundamental study on a model system presented in this work is key to understanding the phase behavior of multiple component microemulsions as well as their design for applications at higher temperatures, where the structure of most RMs breaks down.

Mixed micelles and gels of a hydrophilic poloxamine (Tetronic 1307) and miltefosine: Structural characterization by small-angle neutron scattering and in vitro evaluation for the treatment of leishmaniasis

Hypothesis/background: Tetronic® is a family of four-armed amphiphilic block copolymers of polyethylene oxide (PEO) and polypropylene oxide (PPO) that self-aggregate to form micelles and hydrogels. Due to their temperature and pH-responsiveness, they are emerging as smart nanomaterials in the area of drug delivery. Here we propose the use of Tetronic 1307 (T1307) as a nanocarrier of miltefosine (MF), a zwitterionic alkylphospholipid highly active against leishmaniasis, one of the most threating neglected tropical diseases. Given the amphiphilic nature of the drug, both surfactants can combine to form mixed micelles, reducing the cytotoxicity of MF by lowering its dose and improving its internalization, hence its antileishmanial effect.Experiments: The structure of the T1307 micelles, MF micelles, mixed micelles and hydrogels, formed in buffered solution (pH = 7.4) at different concentrations has been investigated in-depth by a combination of small-angle neutron scattering (SANS), dynamic light scattering (DLS), fluorescence spectroscopy and nuclear magnetic resonance methods (1D, 2D NOESY, and diffusion NMR). The cytotoxicity of the aggregates in macrophages has been assessed, as well as the antileishmanial activity in both Leishmania major promastigotes and amastigotes.Findings: T1307 and MF combine into mixed aggregates over a wide range of temperatures and compositions, forming ellipsoidal core–shell mixed micelles. The shell is highly hydrated and comprises most of the PEO blocks, while the hydrophobic core contains the PO blocks and the MF along with a fraction of EO and water molecules, depending on the molar ratio in the mixture. The combination with T1307 amplified the leishmanicidal activity of the drug against both forms of the parasite and dramatically reduced drug cytotoxicity. T1307 micelles also showed a considerable leishmanicidal activity without exhibiting macrophage toxicity. These results support the use of T1307 as a MF carrier for the treatment of human and animal leishmaniasis, in its different clinical forms.

Model of Fractal Organization of Chromatin in Two-Dimensional Space

Chromatin, consisting of a meter-long DNA strand and associated proteins, is packed into the nucleus of a biological cell tightly but without entanglement. There is a hypothesis, confirmed by experiments involving the chromatin conformation capture technology [1], that curves densely filling the space (Peano or Hilbert curves) provide a good theoretical model to describe the chromatin packing into the nucleus. However, small-angle neutron scattering (SANS) experiments show a bifractal organization of chromatin in the interphase nucleus, thus demonstrating the presence of a logarithmic fractal on larger scales and a volume fractal on smaller scales [2]. In this paper, numerical Fourier analysis in the two-dimensional space is applied to simulate neutron scattering, and a model of a unified bifractal object is presented. It is shown that, in numerical radiation scattering experiments in the two-dimensional space, the mass and logarithmic fractals are significantly different from space-filling curves and from nonfractal objects. For instance, for a logarithmic fractal with a Hausdorff dimension of 2, scattering intensity decreases with increasing Fourier coordinate q by the power law q–2. For curves filling the two-dimensional space, the intensity decreases by the power law q–3, just as for nonfractal objects with sharp boundary in the plane. Thus, first, it is demonstrated that the model of space-filling curves is inadequate to describe the chromatin packing into the nucleus of a biological cell; second, a model of a unified bifractal object is proposed that combines logarithmic and mass fractals on different scales; and, third, a model of chromatin packing is proposed that can describe the data of both small-angle neutron scattering experiments and experiments involving chromatin conformation capture technology.

Insights into the CO2 Capture Characteristics within the Hierarchical Pores of Carbon Nanospheres Using Small-Angle Neutron Scattering.

Understanding adsorption processes at the molecular level has transformed the discovery of engineered materials for maximizing gas storage capacity and kinetics in adsorption-based carbon capture applications. In this work, we studied the molecular mechanism of gas (CO2, H2, methane, and ethane) adsorption inside an interconnected porous network of carbon. This was achieved by synthesizing novel macro-meso-microporous carbon (M3C) nanospheres with interconnected pore structures. The M3Cs showed a CO2 capture capacity of 5.3 mmol/g at atmospheric CO2 pressure, with excellent kinetics. This was due to fast CO2 adsorption within the interconnected hierarchical macro-meso-microporous M3C. In situ small-angle neutron scattering (SANS) under various CO2 pressures indicated that the macro- and mesopores of M3C enable fast diffusion of CO2 molecules inside the micropores, where adsorbed CO2 molecules densify into a liquid-like state. This strong densification of CO2 molecules causes fast CO2 diffusion in the macro- and mesopores of M3C, restarting the adsorption cycle for fresh CO2 molecules until all pores are completely filled. Notably, M3C also showed good capture capacities for hydrogen and various hydrocarbons, with excellent selectivity toward ethane over methane.