Kaczmarski Krzysztof, Bellot Jean-Christophe
Faculty of Chemistry, Rzeszow University of Technology, ul. W. Pola 2, 35-959 Rzeszow, Poland.
Biotechnol Prog. 2004 May-Jun;20(3):786-92. doi: 10.1021/bp034283l.
The general rate model was developed and solved to describe protein adsorption in an expanded bed. The model takes into account axial variation of bed porosity, particle size distribution (PSD), external and intraparticle mass transfer, and dispersion in liquid and solid phase. The analysis of the influence of the model parameters on dynamic capacity (DC) was investigated. The simulation results showed that major impact on dynamic capacity is exerted by intraparticle mass transfer (particle diameter and pore diffusivity). The external mass transfer resistance and dispersion parameters have secondary effect on DC. The replacement of axial PSD by the mean particle diameter results in error in calculation of DC, which increases remarkably with the increase of mean particle diameter. The PSD can promote a very slow approaching of plateau concentration by breakthrough curves. It was shown also that axial bed porosity variation could be replaced by average porosity with negligible error for DC calculations.
开发并求解了通用速率模型,以描述膨胀床中的蛋白质吸附。该模型考虑了床层孔隙率的轴向变化、粒径分布(PSD)、颗粒外部和内部的传质以及液相和固相中扩散。研究了模型参数对动态容量(DC)的影响。模拟结果表明,颗粒内部传质(粒径和孔隙扩散率)对动态容量有主要影响。外部传质阻力和扩散参数对DC有次要影响。用平均粒径代替轴向PSD会导致DC计算出现误差,该误差随着平均粒径的增加而显著增大。PSD可使穿透曲线的平台浓度非常缓慢地趋近。研究还表明,对于DC计算,用平均孔隙率代替轴向床层孔隙率变化所产生的误差可忽略不计。