In isotachophoresis (ITP), the sample constituents migrate, depending on their concentrations in the loaded sample, either in fully developed zones or in the boundary layers between the zones of constituents of the corresponding effective mobilities. The latter (spike) migration mode is analytically beneficial in selective detections of trace analytes, especially, when appropriately chosen discrete spacers minimize detection interferences due to matrix constituents. To facilitate a search for suitable mixtures of discrete spacers, a two-step calculation procedure was developed in this work. Using a pool of discrete spacers consisting of 42 anionic and zwitterionic constituents, this procedure was shown effective in the anionic ITP separations performed at pH = 6.5-10.0. Besides the predictions of the migration orders, it was helpful in identifying the spacing constituents that could cause resolution problems due to an uncertainty with which pH of the leading electrolyte solution is known. The ionic mobility and pKa data, taken for the spacing constituents from the literature and the ones obtained from the ITP experiments carried out in this work, were used in the calculations performed in a context with the choice of spacers. Although the data obtained from the ITP experiments provided better results, small uncertainties with which they were acquired (attributable to fluctuations in the experimental conditions) set practical limits in the calculation based choice of multi-component mixtures of the spacing constituents.
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http://dx.doi.org/10.1016/j.chroma.2003.08.030 | DOI Listing |
Soft Matter
December 2024
Department of Applied Chemistry, School of Chemistry and Chemical Engineering, Yantai University, Yantai 264006, China.
Nanomaterials (Basel)
October 2024
Department of Physics and Astronomy, University of Western Ontario, London, ON N6A 3K7, Canada.
Concentric multiple nanorings have previously been fabricated and investigated mainly for their different static magnetization states. Here, we present a theoretical analysis for the magnetization dynamics in double nanorings arranged concentrically, where there is coupling across a nonmagnetic spacer due to the long-range dipole-dipole interactions. We employ a microscopic, or Hamiltonian-based, formalism to study the discrete spin waves that exist in the magnetic states where the individual rings may be in either a vortex or an onion state.
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December 2024
Water Desalination and Reuse Center, Biological and Environmental Science and Engineering Division (BESE), King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia.
OCT imaging is an important technique to study fouling in spacer-filled channels of reverse osmosis systems for seawater desalination. However, OCT imaging of membrane filtration channels with feed spacers is challenging because the spacer material can be (partly) transparent, making it difficult to detect and possibly mistaken for fouling, and the longer optical pathway through the spacer material distorts the image below the spacer. This study presents an automated 3D OCT image processing method in MATLAB for visualization and quantification of biofouling in spacer-filled channels.
View Article and Find Full Text PDFPolymers (Basel)
July 2024
Theory & Simulation Laboratory, Department of Chemistry, Jamia Millia Islamia (A Central University), New Delhi 110025, India.
This review utilizes an optimized Rouse-Zimm discrete hydrodynamic model and the preaveraged Oseen tensor, which accurately consider hydrodynamic interactions to study model dendrimers. We report the analytical theories that have been previously developed for the creation of generalized analytical models for dendrimers. These generalized theories were used to assess the conformational and dynamical behavior of the dendrimers.
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October 2024
Departamento de Química Inorgánica, Instituto de Ciencia Molecular. Universidad de Valencia, Calle Catedrático José Beltrán 2, 46980 Paterna, Valencia, Spain.
The Cu complexes of three [1 + 1] azacyclophane macrocycles having the 1-pyrazole ring as the spacer and the pentaamine 1,5,8,11,15-pentaazadecane (L1) or hexaamines 1,5,8,12,15,19-hexaazanonadecane (L2) and 1,5,9,13,17,21-hexaazaheneicosane (L3) as bridges show endo- coordination of the pyrazolate bridge giving rise to discrete monomeric species. Previously reported pyrazolacyclophanes evidenced, however, exo-coordination with the formation of dimeric species of 2 : 2, 3 : 2 or even 4 : 2 Cu : L stoichiometry. The complexes have been characterized in solution using potentiometric studies, UV-Vis spectroscopy, paramagnetic NMR, cyclic voltammetry and mass spectrometry.
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