A model to estimate the size of nanoparticle agglomerates in gas-solid fluidized beds

被引:35
作者
de Martin, Lilian [1 ]
van Ommen, J. Ruud [1 ]
机构
[1] Delft Univ Technol, Dept Chem Engn, NL-2628 BL Delft, Netherlands
基金
欧洲研究理事会;
关键词
Van der Waals; Hydrogen bond; Fluidization; Aggregates; Interaction; Nanoparticle processing; Modeling and simulation; NANO-PARTICLE FLUIDIZATION; INTERPARTICLE FORCES; EQUATION; ADHESION; BEHAVIOR;
D O I
10.1007/s11051-013-2055-x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The estimation of nanoparticle agglomerates' size in fluidized beds remains an open challenge, mainly due to the difficulty of characterizing the inter-agglomerate van der Waals force. The current approach is to describe micron-sized nanoparticle agglomerates as micron-sized particles with 0.1-0.2-mu m asperities. This simplification does not capture the influence of the particle size on the van der Waals attraction between agglomerates. In this paper, we propose a new description where the agglomerates are micron-sized particles with nanoparticles on the surface, acting as asperities. As opposed to previous models, here the van der Waals force between agglomerates decreases with an increase in the particle size. We have also included an additional force due to the hydrogen bond formation between the surfaces of hydrophilic and dry nanoparticles. The average size of the fluidized agglomerates has been estimated equating the attractive force obtained from this method to the weight of the individual agglomerates. The results have been compared to 54 experimental values, most of them collected from the literature. Our model approximates without a systematic error the size of most of the nanopowders, both in conventional and centrifugal fluidized beds, outperforming current models. Although simple, the model is able to capture the influence of the nanoparticle size, particle density, and Hamaker coefficient on the inter-agglomerate forces.
引用
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页数:9
相关论文
共 31 条
[1]   Comparisons of Hamaker constants for ceramic systems with intervening vacuum or water: From force laws and physical properties [J].
Ackler, HD ;
French, RH ;
Chiang, YM .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1996, 179 (02) :460-469
[2]   Fine cohesive powders in rotating drums: Transition from rigid-plastic flow to gas-fluidized regime [J].
Castellanos, A ;
Valverde, JM ;
Quintanilla, MAS .
PHYSICAL REVIEW E, 2002, 65 (06) :1-061301
[3]   The relationship between attractive interparticle forces and bulk behaviour in dry and uncharged fine powders [J].
Castellanos, A .
ADVANCES IN PHYSICS, 2005, 54 (04) :263-376
[4]   EFFECT OF INTERPARTICLE FORCES ON THE HYDRODYNAMIC BEHAVIOR OF FLUIDIZED AEROGELS [J].
CHAOUKI, J ;
CHAVARIE, C ;
KLVANA, D .
POWDER TECHNOLOGY, 1985, 43 (02) :117-125
[5]  
de Martin L, 2012, B AM PHYS SOC, V57
[6]  
Espin MJ, 2009, PHYS REV E, V79, p011 304
[7]   A simple model incorporating the effects of deformation and asperities into the van der Waals force for macroscopic spherical solid particles [J].
Forsyth, AJ ;
Rhodes, MJ .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2000, 223 (01) :133-138
[8]   FULL SPECTRAL CALCULATION OF NONRETARDED HAMAKER CONSTANTS FOR CERAMIC SYSTEMS FROM INTERBAND TRANSITION STRENGTHS [J].
FRENCH, RH ;
CANNON, RM ;
DENOYER, LK ;
CHIANG, YM .
SOLID STATE IONICS, 1995, 75 :13-33
[9]  
Friedlander SK., 2000, SMOKE DUST HAZE, VVol. 198
[10]  
Israelachvili JN, 2011, INTERMOLECULAR AND SURFACE FORCES, 3RD EDITION, P1