Characterisation of large scale structures in starch granules via small-angle neutron and X-ray scattering

2013 ◽  
Vol 91 (1) ◽  
pp. 444-451 ◽  
Author(s):  
James Doutch ◽  
Elliot P. Gilbert
2001 ◽  
Vol 34 (1) ◽  
pp. 62-64 ◽  
Author(s):  
Jan van der Elsken ◽  
Wim Bras ◽  
Jan Michielsen

Small-angle X-ray scattering experiments reveal the formation of large-scale structures when a 60 wt% poly(vinylpyrrolidone) (PVP)–water mixture is cooled to 260 K. The formation of these structures leads to an enhancement of continuous small-angle scattering with decreasing temperature. This is accompanied by the appearance of sharp Bragg peaks that have a very short lifetime. The scattering angles of these peaks are in accordance with a hexagonal columnar structure. It appears that such structures occasionally live long enough to undergo rotational Brownian motion.


1991 ◽  
Vol 24 (6) ◽  
pp. 1027-1034 ◽  
Author(s):  
J. P. Simon ◽  
O. Lyon

A large rapidly decreasing intensity called the `scattering tail' is generally observed at the smallest recorded angles during small-angle measurements of metallic alloys. Since this tail was interpreted as caused by a bimodal phase separation in Cu–Ni–Fe alloys and by long-wavelength concentration fluctuations in Invar alloys, these two systems were re-examined with anomalous X-ray scattering. The variation of the alloying atomic contrasts allows a discrimination between the different types of particles or defects. In neither of the two systems can the tails be interpreted as caused by large-scale concentration fluctuations. In Cu–Ni–Fe alloys, the tail is due to some kind of superficial defect (surface roughness etc.). In Invar alloys, the tail is probably due to residual impurity particles.


2016 ◽  
Vol 55 ◽  
pp. 228-234 ◽  
Author(s):  
Takashi Ichihara ◽  
Junya Fukuda ◽  
Takeshi Takaha ◽  
Shiho Suzuki ◽  
Yoshiaki Yuguchi ◽  
...  

2014 ◽  
Vol 70 (a1) ◽  
pp. C404-C404
Author(s):  
Dmitry Svergun

Small-angle X-ray scattering (SAXS) experiences a renaissance in the studies of macromolecular solutions allowing one to study the structure of native particles and complexes and to rapidly analyze structural changes in response to variations in external conditions. New high brilliance sources and novel data analysis methods significantly enhanced resolution and reliability of structural models provided by the technique (Graewert & Svergun, 2013). Automation of the experiment, data processing and interpretation make solution SAXS a streamline tool for large scale structural studies in molecular biology. The recent developments will be presented including robotic sample changers, pipelines for data processing, computation of structural parameters and ab initio models, classification of the folding states of macromolecules. A prototype of an expert systems allowing for automated generation and assessment of structural models will be considered. A synergistic use of SAXS with the high resolution methods like crystallography and NMR, but also with complementary biophysical and biochemical techniques will be discussed. The problems of validation of SAXS-generated models, and the use of data quality assessment tools for the deposition of the models and experimental data will be discussed. Further perspectives of the hybrid applications of SAXS with other techniques in structural biology will be outlined.


2019 ◽  
Vol 26 (5) ◽  
pp. 1412-1421 ◽  
Author(s):  
Sen Chen ◽  
Hai-Wei Chai ◽  
An-Min He ◽  
Thomas Tschentscher ◽  
Yang Cai ◽  
...  

High-brightness coherent ultrashort X-ray free-electron lasers (XFELs) are promising in resolving nanoscale structures at the highest temporal resolution (∼10 fs). The feasibility is explored of resolving ultrafast fragmentation of liquids at the nanoscale with single-shot small-angle X-ray scattering (SAXS) on the basis of large-scale molecular dynamics simulations. Fragmentation of liquid sheets under adiabatic expansion is investigated. From the simulated SAXS patterns, particle-volume size distributions are obtained with the regularization method and average particle sizes with the weighted Guinier method, at different expansion rates. The particle sizes obtained from simulated SAXS are in excellent agreement with direct cluster analysis. Pulse-width effects on SAXS measurements are examined. The results demonstrate the feasibility of resolving the nanoscale dynamics of fragmentation and similar processes with SAXS, and provide guidance for future XFEL experiments and data interpretation.


2020 ◽  
Vol 53 (5) ◽  
pp. 1376-1386
Author(s):  
Renata Avena Maia ◽  
Leonardo Simões de Abreu Carneiro ◽  
Jhonny Mauricio Cerón Cifuentes ◽  
Camilla Djenne Buarque ◽  
Pierre Mothé Esteves ◽  
...  

Small-angle X-ray scattering (SAXS) is an accurate nondestructive method that requires a minimum of sample preparation and is employed to study porosity, morphology and hierarchical structures. Zeolites and silica are among the porous materials that are widely investigated by SAXS. However, studies of covalent organic frameworks (COFs) are still scarce. In the present study, SAXS was employed to investigate meso- and microporous COFs, affording insightful information about their nanostructure textural properties. SAXS is especially useful when combined with other characterization techniques, such as powder X-ray diffraction and N2 adsorption isotherms, emerging as an efficient tool to further characterize COFs. For microporous COFs, SAXS was used mainly to obtain quantitative values of surface roughness as a function of fractal parameters, in all cases indicating surface fractals of the large-scale scattering object, namely the `grain'. Mesoporous COF studies allowed elucidation of their hexagonal structure on the basis of their structure peaks; however, the main result lies in the distinction between the pore and the grain, which are described as a hierarchical structure by the Beaucage model and evaluated according to their fractality. These COFs generally exhibit pores with mass fractal features and grains with surface fractal features when they are submitted to post-functionalization, which may be due to the poor diffusivity of the functionalizing agents into the pores. In addition, a proposed aggregation description of the porous scattering objects was envisioned, based on small-angle scattering premises, which was confirmed for a microporous COF by high-resolution transmission electron microscopy.


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