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1.
J Sep Sci ; 31(12): 2219-30, 2008 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-18615827

RESUMO

Recent and earlier models of electrical field flow fractionation (ELFFF) have assumed that the electric field within the fluid domain is governed by Laplace's equation. This assumption results in a linear potential and a spatially constant field across the channel and is generally true for very dilute systems and relatively high effective potentials. Experimental studies show, however, that the effective potential within the channel may be less than 1% of the applied potential; this is apparently due to double layer formation and charge buildup at the poles. In such cases, local analyte concentrations can, nonetheless, be orders of magnitude higher than the bulk mean and the local potential small, both of which can lead to a nonlinear spatial distribution of the field strength. In such cases Poisson's equation must be used rather than Laplace's equation. Steady-state ELFFF simulations were performed using a Poisson's equation-based model. The domain in which Laplace's equation is valid was identified and the effects of concentration and effective field strength on device performance were explored.

2.
Anal Chem ; 78(14): 4998-5005, 2006 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-16841923

RESUMO

In electrical field flow fractionation (EFFF or ElFFF), an electric potential is applied across a narrow gap filled with a weak electrolyte fluid. Charge buildup at the two poles (electrodes) and the formation of an electric double layer shields the channel, making the effective field in the bulk fluid very weak. Recent computational research suggests that pulsed field protocols, however, should improve retention and may enhance separation in EFFF through systematic disruptions of the double layer resulting in a stronger effective field in the bulk fluid. Improved retention has already been demonstrated experimentally. Accurate modeling and subsequent device optimization and design, however, depends, in part, on formulating a suitable model for the capacitative response of the channel and double layer at the electrode surfaces. Early models do not correctly describe experimentally observed current-time response and are not physically meaningful even when accurate mathematical fits of the data are realized. A new model and conceptual framework based on electrical resistance and capacitance variations of the double layer is suggested here. Physical interpretations of the electrical response have been developed and compared to published experimental data sets.


Assuntos
Elétrons , Fracionamento por Campo e Fluxo/instrumentação , Fracionamento por Campo e Fluxo/métodos , Modelos Químicos , Eletroquímica , Fatores de Tempo
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