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1.
Anal Chem ; 90(23): 13978-13986, 2018 12 04.
Artículo en Inglés | MEDLINE | ID: mdl-30376711

RESUMEN

Asymmetrical flow field-flow fractionation (AF4) is a chromatographic separation technique that can be used for a broad range of particles or macromolecules. As an orthogonal method to size exclusion chromatography (SEC) with a much broader separation size range (1-800 nm) AF4 is gaining importance. However, the data evaluation capacities are far behind in comparison to other techniques like analytical ultracentrifugation (AUC). A program for evaluation of data from AF4 with a coupled multiangle laser light scattering (MALLS) detector was developed that allows the determination of the distributions of diffusion coefficients ( D), hydrodynamic radii ( Rh), molecular weights ( Mw), and relative concentrations (RC) of the obtained species. In addition, two algorithms to remove broadening effects via deconvolution were implemented and tested for their validity. The first is an extension of the known diffusion broadening correction applying the entire diffusion coefficient distribution instead of a single diffusion coefficient. The second applies the Richardson-Lucy algorithm for the deconvolution of overlapping signals from stars in astronomy. This program allows a reproducible strong enhancement of the fractogram resolution allowing for entire baseline separations of proteins. The comparison of the values for Mw determined by a partial Zimm plot from each data point of the original fractogram and the deconvolved results shows that especially the Richardson-Lucy algorithm maintains a high degree of data robustness.

2.
Small ; 13(34)2017 09.
Artículo en Inglés | MEDLINE | ID: mdl-28722343

RESUMEN

One efficient method to obtain disordered colloidal packing is to reduce the stability of colloidal particles by adding electrolytes to the colloidal dispersions. But the correct amount of additional electrolytes must be found empirically. Here, the effect of CaCl2 on polystyrene colloidal dispersions is studied, and a link between the amount of CaCl2 and the corresponding glassy colloidal structure is quantitatively built. A threshold concentration of CaCl2 is found by dynamic light scattering. When exceeding this threshold, different nanoparticle oligomers are observed in the dispersions by analytical ultracentrifugation. The second objective is to achieve free-standing samples, which is required for many optical measurements. A universal method is established, using a centrifugal field to produce robust samples by polymerizing coassembled hydrophilic monomers to form a network, which traps the glassy colloidal structures. Photon time of flight measurements shows that the CaCl2 concentration threshold should not be exceeded. Otherwise an optical shortcut may take place. Thus, the work provides a feasible universal route to prepare macroscopic free-standing photonic glasses from electrostatically stabilized nanoparticles, suitable for further optical investigation.

3.
J Chromatogr A ; 1635: 461631, 2021 Jan 04.
Artículo en Inglés | MEDLINE | ID: mdl-33260023

RESUMEN

Asymmetrical flow field-flow fractionation is a versatile chromatographic fractionation method. In combination with at least one detection technique it is used for size-based separation of colloids, biomolecules and polymers. Although often used as pure separation method, a well-elaborated theory is available that allows precise quantification of the translational diffusion coefficient D. Still, current literature suggests different ways to transform this theory into applicable experimental procedures and no "gold standard" for correct data processing exists. While some sources report a direct way to extract diffusion information from the fractogram, others suggest the necessity of an external calibration measurement to obtain the channel width w. In this work, we compare the different approaches and calibration algorithms based on original and literature data using our own open-source AF4 evaluation software. Based on the results, we conclude that available AF4 setups do not fulfill the requirements for absolute measurements of D. We show that the best way to conduct is to consider the area of the channel and D of the calibrant while neglecting the small peak which occurs in the void peak region.


Asunto(s)
Calibración/normas , Técnicas de Química Analítica/métodos , Fraccionamiento de Campo-Flujo , Algoritmos , Técnicas de Química Analítica/normas , Difusión , Tamaño de la Partícula , Polímeros/química
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