Search Results (1,072)

Lignin nanoparticles (LNPs) offer sustainable alternatives to petroleum-derived nanofillers, yet their industrial application remains limited by poor dispersion control and trade-offs between loading, optical clarity, and mechanical performance. Here, we present a molecular architecture-driven design framework that systematically decouples polymer network physics from nanoparticle dispersion in poly(vinyl alcohol)/LNP nanocomposites. Through eco-friendly self-precipitation, we synthesize uniform LNPs with size tunability, overcoming persistent reproducibility challenges. Systematic investigation across PVA molecular weights and LNP loadings reveals entanglement-controlled dispersion behavior. Combined rheological and small-angle X-ray scattering analyses demonstrate that macroscopic suspension rheology is governed exclusively by polymer chain overlap, remaining invariant across LNP loadings. Conversely, the nanoscale LNP microstructural organization—ranging from depletion-driven clustering in weakly entangled networks to network-confinement stabilization in densely entangled systems—fundamentally dictates the film’s optical clarity and mechanical toughness. This rheology-microstructure decoupling establishes critical processing windows for industrial formulations, where polymer entanglement ensures suspension processability while the LNP dispersion state enables optical–mechanical tunability. The entangled network’s structure-filtering effect provides robust protocols for fabricating sustainable, transparent bio-composites suitable for packaging, optics, and functional films. Our quantitative composition–structure–performance framework advances fundamental understanding of entanglement-mediated interfacial phenomena while delivering practical design rules for next-generation sustainable bio-composites. Full article

Polarimetric information is essential for scattering interpretation and target characterization in synthetic aperture radar (SAR) remote sensing, yet many resource-constrained platforms (e.g., small satellites and unmanned aerial vehicles (UAVs)) operate with limited polarization modes or even a single radio frequency (RF) chain, which limits full polarimetric scattering acquisition. To address this limitation, this paper proposes a single-channel framework for estimating the full polarization scattering matrix (PSM) enabled by time-varying polarization modulation. The transmit/receive polarization states are steered along predefined trajectories on the Poincaré sphere to generate time-varying polarization tags that are encoded into the received echoes through the target’s polarization-varying response. A compact observation model is then derived to relate the single-channel echoes, the known polarization tags, and the unknown PSM; based on this, the PSM is then estimated via a least squares formulation with a low-rank approximation. Simulation results demonstrate the robust reconstruction of the full polarimetric scattering matrix under diverse modulation trajectories. For arbitrarily chosen random point targets, when the signal-to-noise ratio (SNR) exceeds −20 dB, the polarimetric similarity coefficient approaches 1, and the estimation errors of Pauli power components converge toward zero. Furthermore, the method’s reliability is validated on distributed vegetation clutter. Quantitative metrics demonstrate near-perfect statistical consistency, with polarimetric entropy and alpha angle errors within 0.14%. Overall, the proposed approach provides a practical pathway to enhance the availability of full polarimetric scattering information under limited-observation conditions, confirming its feasibility for downstream analysis in complex natural scenes while maintaining a single radio frequency (RF) chain architecture augmented by a polarization modulator. Full article

Linalyl acetate is a key bioactive component of essential oils with notable calming and sedative effects; however, its high volatility severely limits stability and practical application. Herein, bimodal mesoporous silica (BMMs) was employed as an efficient carrier to encapsulate linalyl acetate using liquid- and gas-phase loading strategies, enabling high loading capacity and sustained release. Under optimized gas-phase conditions (600 mg·mL⁻¹, 85 °C, 2 h), a maximum loading capacity of 80.13% was achieved. The X-ray diffraction (XRD) and small-angle X-ray scattering (SAXS) patterns, scanning electron microscopy (SEM) images, N₂ adsorption–desorption isotherms, Fourier transform infrared (FT-IR) spectra, and thermogravimetric (TG) performances confirmed the successful confinement of linalyl acetate within the bimodal mesoporous channels. Particularly, the SAXS patterns revealed the pronounced fractal characteristics, whereas the increased mass-fractal dimension (D_m) values indicated the enhanced structural compactness, and higher surface-fractal dimension (D_s) values reflected increased surface roughness upon loading. Release experiments conducted in an open environment demonstrated an excellent sustained-release performance, with only 22.41% of linalyl acetate released from BMMs over 30 days, compared with 94.41% for the free compound. Molecular dynamics simulations further elucidated that the interactions between linalyl acetate molecules and surface silanol groups dominated the adsorption process and governed diffusion within the mesoporous channels. These findings suggested that BMMs provide a robust platform for stabilizing volatile fragrance compounds and achieving long-term controlled release. Full article

We investigated the high-temperature tensile and creep properties of highly strong heat-elongated polypropylene (elongated PP) before and after long annealing for 21 days at a high temperature of 120 °C. Despite the thermal deterioration caused by the long annealing, the elongated PP exhibited high tensile strength. The yield stress values of the elongated and long-annealed (LA)-elongated PP obtained from engineering stress–strain curves were 60 MPa and 102 MPa, respectively, at 120 °C, whereas that of the unelongated PP was 8 MPa. Due to the suppression of crystalline chain motion at high temperature caused by the presence of crystalline fibrils connected to lamellae, as indicated by the high elastic modulus observed using a dynamic mechanical analyzer, the elongated PP also exhibited excellent high-temperature creep properties despite thermal deterioration. Small-angle X-ray scattering and DSC measurements revealed that lamellae were fragmented in the elongated PP, while the fragmentation of lamellae was suppressed in the LA-elongated PP during tensile stretching and creep. These characteristic deformation behaviors might also provide excellent high-temperature properties. The excellent high-temperature properties of the elongated PP are promising for industrial applications that require resistance to high temperatures. Full article

Background: Pentamidine isethionate (PTM) and miltefosine (MF) are clinically relevant antiparasitic agents whose use is limited by toxicity, emerging resistance, and the lack of effective co-delivery strategies. Tetronic^® 1307 (T1307), an amphiphilic and thermoresponsive block copolymer, was investigated as a carrier to enable their combination therapy. Methods: PTM and MF were formulated in T1307-based micelles and thermoresponsive gels. The systems were characterized by small-angle neutron scattering (SANS), dynamic light scattering (DLS), and nuclear magnetic resonance spectroscopy (NMR). Antiparasitic activity was evaluated against Leishmania major promastigotes. Results: MF formed stable micelles that efficiently incorporated PTM, generating a “drug-in-drug” architecture. While T1307 alone showed limited PTM loading, MF promoted mixed micelle formation and enhanced PTM incorporation. At physiological temperature and adequate copolymer concentrations, drug-loaded micelles formed thermoreversible gels suitable for topical application. The combined formulations preserved drug activity and exhibited synergistic effects against L. major. Conclusions: T1307 is a promising platform for the co-delivery of PTM and MF, enabling synergistic combination therapy and thermoresponsive gel formation with potential to reduce systemic toxicity and improve treatment administration. Full article

Characterization of shale pore architecture forms the scientific basis for effective shale gas exploitation. Deep LMX FM shale from the Luzhou area was analyzed using SANS, LTPA, XRD, and SEM. This study quantitatively characterized the pore structure, focusing on closed-pore development and connectivity, and explored lithological controls. Pore-size distribution shows that micropores and small mesopores dominate the pore volume, with an average median pore diameter of 5.17 nm. Closed pores are abundant, indicated by a high average closed-pore ratio of 28.98%, reflecting generally poor connectivity. Pores smaller than 5 nm contribute 88.12% of the total SSA. Both pore volume and SSA correlate positively with TOC. In organic-rich and moderately organic-rich siliceous shales, these parameters also correlate positively with quartz content. In contrast, for organic-rich mixed shales, they correlate positively with clay mineral content. Among the lithofacies, organic-rich siliceous shale possesses relatively larger pore volume and SSA, along with better pore connectivity, making it the most favorable reservoir facies. Based on pore-structure characteristics and the regional structural setting, we recommend adopting close-spacing hydraulic fracturing with reduced cluster spacing in structurally stable areas to enhance stimulation. In structurally complex areas, engineering designs should prioritize risk mitigation to ensure operational success. Full article

Germination is widely recognized as an effective strategy to enhance the nutritional quality and reduce anti-nutritional factors in plant foods. This study evaluated the impact of germination on Cruciferous vegetables (family Cruciferae or Brassicaceae) broccoli and kale by assessing changes in proximate composition, macro- and microelement profiles, total and individual polyphenols, phytic acid content, antimicrobial activity, and structural characteristics using Fourier Transform Infrared Spectroscopy (FTIR) and Small- and Wide-Angle X-ray Scattering (SAXS/WAXS) analyses. Germination significantly increased protein content (30.33% in broccoli sprouts and 30.21% in kale sprouts), total phenolic content (424.40 mg/100 g in broccoli sprouts and 497.94 mg/100 g in kale sprouts), and essential minerals, while reducing phytic acid levels in both species (up to 82.20%). Antimicrobial effects were matrix-dependent, being detected in broccoli and kale seed powders, while no inhibitory activity was observed for the corresponding sprout powders under the tested conditions. FTIR spectra indicated notable modifications in functional groups related to carbohydrates, proteins, and phenolic compounds, while SAXS analysis revealed structural reorganizations at the nanoscale. Overall, germination improved the nutritional and phytochemical quality of broccoli and kale while decreasing anti-nutritional compounds, highlighting its potential to enhance the health-promoting value of Brassica sprouts. Full article

Herein, we propose a simple and cost-effective method for fabricating moderate-sensitivity surface-enhanced Raman scattering (SERS) substrates using Cu-plasma polymer fluorocarbon (Cu-PPFC) nanocomposite films fabricated through RF sputtering. The use of a composite target composed of carbon nanotube (CNT), Cu, and polytetrafluoroethylene (PTFE) powders (5:60–80:35–15 wt%) offers the advantage of the simple fabrication of moderate-sensitivity SERS substrates with a single cathode compared to co-sputtering. X-ray photoelectron spectroscopy (XPS) revealed that the film surface was partially composed of metallic Cu with Cu-F bonds and Cu–O bonds, confirming the coexistence of the conducting and plasmon-active domains. UV-VIS spectroscopy revealed a distinct absorption peak at approximately 680 nm, indicating the excitation of localized surface plasmon resonances in the Cu nanoclusters embedded in the plasma polymer fluorocarbon (PPFC) matrix. Atomic force microscopy and grazing incidence small-angle X-ray scattering analyses confirmed that the Cu nanoparticles were uniformly distributed with interparticle distances of 20–35 nm. The Cu-PPFC nanocomposite film with the highest Cu content (80 wt%) exhibited a Raman enhancement factor of 2.18 × 10⁴ for rhodamine 6G, demonstrating its potential as a moderate-sensitivity SERS substrate. Finite-difference time-domain (FDTD) simulations confirmed the strong electromagnetic field localization at the Cu-Cu nanogaps separated by the PPFC matrix, corroborating the experimentally observed SERS enhancement. These results suggest that a Cu-PPFC nanocomposite film, easily fabricated using a composite target, provides an efficient and scalable route for fabricating reproducible, inexpensive, and moderate-sensitivity SERS substrates suitable for practical sensing applications. Full article

Although membrane proteins are of major importance in both physiology and disease, they remain less studied than soluble proteins due to the complex amphiphilic environments required to preserve their structure and function. As a consequence, membrane proteins are under-represented in structural databases. In this work, we present a robust structural characterization of lipid nanodiscs designed to facilitate membrane protein studies by small-angle neutron scattering. By combining small-angle X-ray and neutron scattering, we investigate nanodiscs of three different sizes and three lipid compositions to accommodate a broad range of systems. Specifically, nanodiscs with diameters of approximately 9 nm, 12 nm, and 15 nm were examined. Beyond the commonly used di-myristoyl-phosphatidylcholine lipid, we produced and characterized polar lipid extracts from a Gram-negative bacterium (Escherichia coli) and a Gram-positive bacterium (Bacillus subtilis) under both protonated and deuterated conditions. In conclusion, solubility-enhanced variants of the scaffold protein yield more stable nanodiscs and are therefore preferable for extended structural investigations. The co-fitting of small-angle scattering data provides robust geometrical models of these nanodiscs, which can be treated as well-defined reference systems for future studies of membrane proteins in native-like lipid environments. Full article

Studying nanoscale self-assembly in real time using external stimuli unlocks new opportunities for dynamic and adaptive materials. While electrostatic self-assembly is well-established, real-time monitoring of its structural evolution under light irradiation remains largely unexploited. In this study, we employ light-responsive azobenzene dyes (Acid Yellow 38, AY38) and pH-sensitive polyamidoamine (PAMAM) dendrimers to investigate the kinetics of electrostatic self-assembly under UV irradiation. Using a custom in situ small-angle neutron scattering (SANS) setup, we track the real-time morphological transformations of self-assembled structures with sub-minute resolution. We introduce two distinct pathways: method A (pre-irradiated cis-AY38 for controlled, slow kinetics) and method B (direct UV-induced self-assembly, fast kinetics). The results reveal that trans-cis isomerization kinetics dictate the rate of self-assembly, influencing aggregate stability, ζ-potential evolution, and final morphology. Structural analysis using dynamic and static light scattering (DLS and SLS) and SANS elucidates a transition from spherical to ellipsoidal morphologies governed by electrostatic and dipole-dipole interactions. These findings establish photoisomerization-driven self-assembly as a robust mechanism for tunable nanoscale architectures, paving the way for adaptive photonic materials, targeted drug delivery, and reconfigurable nanostructures. Full article

SA 178 grade C carbon steel is a material commonly used in boiler tubes. Boilers are crucial in the energy industry; however, their service life degrades over time. If a boiler malfunctions, processing operations must be halted, resulting in financial losses for the company. The aim of this study is to examine the effect of microstructural evolution, especially the transformation of lamellar pearlite into spheroidized pearlite, on the service life degradation of boiler tubes. Understanding these changes is essential for preventing catastrophic system failures. The methodology involves the use of Small-Angle X-ray Scattering (SAXS) supported by metallographic analysis, Scanning Electron Microscopy (SEM), Energy-Dispersive X-ray (EDX) Spectroscopy, and mechanical testing. The SAXS results indicate that the microstructure of SA 178, which initially consisted of ferrite and lamellar pearlite, gradually transforms into spheroidized pearlite. These microstructural changes lead to reductions in tensile strength from 523 MPa for 0% spheroidization to 335 MPa for 100% spheroidization, as well as a reduction in hardness from 175 HV to 89 HV, ultimately decreasing the service life of the boiler tube. Full article

Lipid-based nanomedicines are already widely used in antitumor therapy and gene delivery. However, their complex structural features demand advanced mesoscopic structural characterization tools for effective research and development (R&D) and quality control. Synchrotron small-angle X-ray scattering (SAXS) is a powerful, non-invasive technique for probing nanoscale membrane organizations, monitoring in situ dynamic membrane assembly, and exploring the interactions of components in lipid-based drug delivery systems, including liposomes, lipoplexes, lipid nanoparticles (LNPs), and lyotropic liquid crystals (LLCs). Recent advances in high-flux synchrotron facilities, high-frequency detectors, and automated SAXS data processing pipelines permit a detailed structural characterization of lamellarity, bilayer spacing, internal phases, core–shell morphology, as well as “pump-probe” dynamic process studies for lipid nanomedicines. Though major challenges remain in sample polydispersity and model fitting, the advances in time-resolved synchrotron SAXS, high-throughput automation, and artificial intelligence (AI)-assisted modeling are rapidly reducing this barrier. This review summarizes SAXS methodology and introduces representative case studies in the field of lipid nanomedicines. The performance of BioSAXS beamline BL19U2 in the Shanghai synchrotron radiation facility (SSRF) and prospects of AI-guided drug screening at BL19U2 are highlighted to advance intelligent R&D and quality control for lipid nanomedicines. Full article

Carbon aerogels (CAs) had been well applied in extreme condition thermal insulation, but achieving a balance between mechanical robustness and thermal insulation remains challenging. We present a novel strategy to fabricate carbon aerogels with tunable mechanical properties and thermal insulation properties by tailoring their skeleton architecture via molecular assembly. Carbon precursor aerogel with thick neck particle packing structure was obtained by strong hydrogen-bonding-induced self-assembly between polyurethane-urea oligomer (PUU) and phenolic resin (PF), and carbon aerogel retained robust interparticle connections after pyrolysis, resulting in excellent mechanical properties. The presence of PUU leads to denser packing of resin molecules, promotes graphitization of the carbon and formation of nanocrystalline structures at 1400 °C, resulting in optimized compression modulus and strength. The closed pore structure of carbon skeleton was further studied by Small-Angle X-ray Scattering (SAXS), while moderate pore width (0.4–0.6 nm) optimizes the balance between strength (110 MPa) and thermal conductivity (0.30 W/(m·K)). This work demonstrates that molecular-level assembly combined with pyrolysis control enables precise tuning of carbon aerogel structures and properties, providing new insights for high-temperature thermal insulation applications. Full article

Chia seed oil, valued for its health-promoting omega-3 and omega-6 fatty acids, is highly susceptible to oxidation. This study employed a multi-technique approach based on electron spin resonance (ESR), low-field nuclear magnetic resonance (LF-NMR), and small-angle X-ray scattering (SAXS) to monitor its oxidative process. ESR identified alkyl (DMPO-•R) and peroxyl (DMPO-•OOR) radicals as primary species derived from unsaturated fatty acids. This was accompanied by a decrease in relaxation time of peak T₂₁, T₂₂, and T₂₃, and the peak area of S₂₁ gradually increased as the heating time increased. The SAXS intensity of chia seed oil at q = 3.4 nm⁻¹ increased markedly after heating for 20 h, and the peak shifted to the low q-region with Δq = 0.6 nm⁻¹, confirming the significant formation of nanoscale aggregates, which correlated with observed increases in oil turbidity. Our findings demonstrate the value of an integrated analytical strategy for a comprehensive understanding of oxidation in chia seed oil. Full article

Proteins play an important role in living organisms, and, for most of them, the function depends on their structure. There are some proteins that have similar properties but different structures. An example of this is ice-binding proteins (IBPs), which have different structures but share the ability to bind to ice. Many organisms have evolved such proteins to help them survive in cold environments. Therefore, it is important to study the oligomeric state of the active form in solutions. The activity of IBP is related to the area of their ice-binding site. We have demonstrated the presence of oligomeric forms of protein in solution using multiple techniques, such as mass spectrometry, native gel electrophoresis, atomic force microscopy (AFM), isothermal titration calorimetry (ITC) and small-angle X-ray scattering (SAXS). It is noteworthy that, to date, there have been no reports of the oligomerization of ice-binding protein from Longhorn sculpin. Additionally, our findings suggest that larger molecules may influence the ability of proteins to bind to ice. In our study, the ice-binding protein forms elongated assemblies with limited intermonomer interfaces. The combination of SAXS and AFM data indicates a structure that combines compactness and flexibility and probably consists of four monomeric units. The employment of molecular modelling methodologies resulted in the attainment of a tetrameric complex that is in alignment with AFM data. Details of oligomers observed using the methods in our study emphasize the importance of different techniques that complement each other in resolving structural features. Additionally, we suggest that the protein particles, which were dispersed on the surface, exhibit softness or the form planar complexes with loose quaternary structures. It is conceivable that, depending on ionic strength and/or temperature, the various oligomeric forms of the ice-binding protein form thermodynamically more favorable complexes than their monomeric forms. Full article