Simulation of Mixing in Structured Fluids with Dissipative Particle Dynamics and Validation with Experimental Data

Author(s):  
Gianluca Boccardo ◽  
Antonio Buffo ◽  
Daniele Marchisio
2018 ◽  
Vol 20 (6) ◽  
pp. 4074-4082 ◽  
Author(s):  
Yun Jin ◽  
Danyi Guo ◽  
Bo Li ◽  
Shouping Xu ◽  
Jiang Cheng ◽  
...  

Self-assembly behaviors of POSS-based triblock copolymers were studied by DPD, and the results were in qualitative agreement with the experimental data.


2019 ◽  
Vol 17 (07) ◽  
pp. 1950032
Author(s):  
Sisi Tan ◽  
Mingze Xu

A biological cell exhibits viscoelastic behavior mainly because its components (membrane and cytoplasm) are viscoelastic, and this is clearly seen when it is stretched and released. The present work numerically studied the shape recovery of a red blood cell (RBC) based on a viscoelastic model at the meso-scale using Dissipative Particle Dynamics (DPD) method. In this model, the RBC membrane is represented by a triangular network of worm-like chains, while the cytoplasm is replaced by a system of DPD particles. This viscoelastic model is validated by examining the stretching deformation of an RBC and comparing with the existing experimental data. Viscoelastic properties of the RBC are then analyzed by stretching an RBC under a 20 pN stretching force, and allowing it to relax. The time to recover its shape upon removal of the stretching force is measured to be 111 and 92.6[Formula: see text]ms for an RBC with and without cytoplasm, and the corresponding membrane viscosity is [Formula: see text] and [Formula: see text] [Formula: see text], respectively. These values, for an RBC with cytoplasm, are closer to experimental data than those for an RBC without cytoplasm, lending support to the model with cytoplasm. Finally, parametric studies are conducted on the membrane elastic and bending moduli. The results show that the shape recovery time decreases with increasing the membrane elastic and bending moduli.


2019 ◽  
Author(s):  
Ting Liu ◽  
Anupam Mishra ◽  
Mohsen Torabi ◽  
Ahmed A. Hemeda ◽  
James Palko ◽  
...  

2005 ◽  
Vol 42 (3) ◽  
pp. 180-183 ◽  
Author(s):  
S. G. Schulz ◽  
U. Frieske ◽  
H. Kuhn ◽  
G. Schmid ◽  
F. Müller ◽  
...  

2021 ◽  
Vol 33 (7) ◽  
pp. 072001
Author(s):  
Liuzhen Ren ◽  
Haibao Hu ◽  
Luyao Bao ◽  
Mengzhuo Zhang ◽  
Jun Wen ◽  
...  

2012 ◽  
Vol 45 (19) ◽  
pp. 8109-8116 ◽  
Author(s):  
Brandon L. Peters ◽  
Abelardo Ramírez-Hernández ◽  
Darin Q. Pike ◽  
Marcus Müller ◽  
Juan J. de Pablo

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Ramin Zakeri

AbstractOne of the unresolved issues in physiology is how exactly myosin moves in a filament as the smallest responsible organ for contracting of a natural muscle. In this research, inspired by nature, a model is presented consisting of DPD (dissipative particle dynamics) particles driven by electro-osmotic flow (EOF) in micro channel that a thin movable impermeable polymer membrane has been attached across channel width, thus momentum of fluid can directly transfer to myosin stem. At the first, by validation of electro-osmotic flow in micro channel in different conditions with accuracy of less than 10 percentage error compared to analytical results, the DPD results have been developed to displacement of an impermeable polymer membrane in EOF. It has been shown that by the presence of electric field of 250 V/m and Zeta potential − 25 mV and the dimensionless ratio of the channel width to the thickness of the electric double layer or kH = 8, about 15% displacement in 8 s time will be obtained compared to channel width. The influential parameters on the displacement of the polymer membrane from DPD particles in EOF such as changes in electric field, ion concentration, zeta potential effect, polymer material and the amount of membrane elasticity have been investigated which in each cases, the radius of gyration and auto correlation velocity of different polymer membrane cases have been compared together. This simulation method in addition of probably helping understand natural myosin displacement mechanism, can be extended to design the contraction of an artificial muscle tissue close to nature.


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