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用于固定化生物催化剂的逆流多级流化床反应器:III. 流体动力学方面

Countercurrent multistage fluidized bed reactor for immobilized biocatalysts: III. Hydrodynamic aspects.

作者信息

Vos H J, van Houwelingen C, Zomerdijk M, Luyben K C

机构信息

Department of Biochemical Engineering, Delft University of Technology, Julianalaan 67, 2628 BC Delft, The Netherlands.

出版信息

Biotechnol Bioeng. 1990 Aug 5;36(4):387-96. doi: 10.1002/bit.260360409.

Abstract

In Parts I and II of this series we described the modelling, design, and operation of a multistage fluidized bed reactor (MFBR) for immobilized biocatalysts. This article deals with those aspects of the MFBR which are different from single-stage fluidized beds which are operated in batch mode with respect to the solids. The semicontinuous transport of the particles requires perfect mixing of the particles in the reactor compartments, because particles are mainly transported from the bottom of these compartments. A large spread in the physical properties of the biocatalyst particles, especially of both size and density, may cause the particles to segregate into layers with different diameter and/or density. This affects the efficient use of the biocatalyst. The properties of the particles are dependent on the immobilization method. The suitability of different methods for possible future application in the MFBR is therefore compared. Because of segregation, successful use of a biofilm catalyst with a nonuniform thickness of the biofilm is doubtful. Experiments in a small scale reactor (+/- 0.1 m diameter) demonstrated that perfect particle mixing is possible using commercially available biocatalyst particles of uniform density. Co-immobilization of the biocatalyst with glass powder in a gel is a simple and effective method of increasing gel density. High density particles allow high liquid flow rates, and thus an improved external mass transfer can be achieved.The distributor plates, which separate the reactor compartments, must allow unhindered transport of particles. Therefore, the holes in these plates must have a diameter of at least 4.5 times that of the largest particles which are present in the particle mixture used. Furthermore, the plates must be designed such that, when scaling-up the reactor, a uniform liquid distribution over the cross-sectional area of the reactor occurs. Large-scale experiments were not carried out, but published correlations, indicate that particle mixing and a uniform liquid distribution can be accomplished in a large-scale reactor under similar flow conditions.

摘要

在本系列的第一部分和第二部分中,我们描述了用于固定化生物催化剂的多级流化床反应器(MFBR)的建模、设计和运行。本文讨论了MFBR与单级流化床不同的那些方面,单级流化床在固体方面以间歇模式运行。颗粒的半连续输送要求在反应器隔室中颗粒完全混合,因为颗粒主要从这些隔室的底部输送。生物催化剂颗粒物理性质的较大差异,特别是尺寸和密度方面的差异,可能导致颗粒分离成具有不同直径和/或密度的层。这会影响生物催化剂的有效利用。颗粒的性质取决于固定化方法。因此,比较了不同方法在MFBR未来可能应用中的适用性。由于分离,具有不均匀生物膜厚度的生物膜催化剂能否成功使用值得怀疑。在小型反应器(直径约0.1米)中进行的实验表明,使用密度均匀的市售生物催化剂颗粒可以实现完美的颗粒混合。将生物催化剂与玻璃粉共固定在凝胶中是提高凝胶密度的一种简单有效的方法。高密度颗粒允许高液体流速,从而可以实现更好的外部传质。分隔反应器隔室的分布板必须允许颗粒不受阻碍地输送。因此,这些板上的孔的直径必须至少是所用颗粒混合物中存在的最大颗粒直径的4.5倍。此外,板的设计应使得在扩大反应器规模时,在反应器的横截面上发生均匀的液体分布。未进行大规模实验,但已发表的关联式表明,在类似的流动条件下,在大型反应器中可以实现颗粒混合和均匀的液体分布。

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