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The Change of Pressure Drop during Large‐Scale Chromatography of Viscous Samples

机译:粘性样品大规模色谱过程中压降的变化

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AbstractThe variation of the inlet pressure during the injection and the elution of a band of a viscous compound, or pressure‐drop profile, was calculated in overloaded elution chromatography, assuming a significant difference between the viscosities of the solvent and the pure solute. The viscosity of the mixture was calculated using the Grunberg—Nissan equation. By means of the numerical integration of the mass balance equation, the concentration profile along the length of the column was calculated. Then, using the instantaneous concentration profile to derive the local viscosity, hence the local pressure gradient, the pressure drop was determined by integrating the local pressure gradient along the column. The change of pressure drop calculated is significant only when the concentration of the injected sample is very high. If a dilute sample is injected, even large sample volumes will not really change the pressure drop. The maximum pressure drop observed in each case is practically independent of the absorption isotherm. The only determining factors are the solute concentration in the sample, the amount of sample injected, and the solute diffusiv
机译:摘要假设溶剂和纯溶质的粘度存在显著差异,在过载洗脱色谱法中计算进样过程中入口压力的变化和粘性化合物条带的洗脱或压降曲线。使用Grunberg-Nissan方程计算混合物的粘度。通过质量平衡方程的数值积分,计算了沿色谱柱长度的浓度分布。然后,利用瞬时浓度分布推导局部粘度,从而推导局部压力梯度,通过对沿柱的局部压力梯度进行积分来确定压降。只有当注入样品的浓度非常高时,计算出的压降变化才显着。如果进样稀释的样品,即使样品量很大,也不会真正改变压降。在每种情况下观察到的最大压降实际上与吸收等温线无关。唯一的决定因素是样品中的溶质浓度、进样量和溶质扩散

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