4.5 Article

Influence of polymer additives on turbulent energy cascading in forced homogeneous isotropic turbulence studied by direct numerical simulations

期刊

CHINESE PHYSICS B
卷 21, 期 11, 页码 -

出版社

IOP PUBLISHING LTD
DOI: 10.1088/1674-1056/21/11/114701

关键词

forced homogenous isotropic turbulence; polymer additives; turbulent energy cascading; drag reduction

资金

  1. National Natural Science Foundation of China [51076036, 51206033]
  2. Foundation for Innovative Research Groups of the National Natural Science Foundation of China [51121004]
  3. Fundamental Research Funds for the Central Universities, China [HIT.BRET2.2010008]
  4. Doctoral Fund of Ministry of Education of China [20112302110020]
  5. China Postdoctoral Science Foundation [2011M500652]

向作者/读者索取更多资源

Direct numerical simulations (DNS) were performed for the forced homogeneous isotropic turbulence (FHIT) with/without polymer additives in order to elaborate the characteristics of the turbulent energy cascading influenced by drag-reducing effects. The finite elastic non-linear extensibility-Peterlin model (FENE-P) was used as the conformation tensor equation for the viscoelastic polymer solution. Detailed analyses of DNS data were carried out in this paper for the turbulence scaling law and the topological dynamics of FHIT as well as the important turbulent parameters, including turbulent kinetic energy spectra, enstrophy and strain, velocity structure function, small-scale intermittency, etc. A natural and straightforward definition for the drag reduction rate was also proposed for the drag-reducing FHIT based on the decrease degree of the turbulent kinetic energy. It was found that the turbulent energy cascading in the FHIT was greatly modified by the drag-reducing polymer additives. The enstrophy and the strain fields in the FHIT of the polymer solution were remarkably weakened as compared with their Newtonian counterparts. The small-scale vortices and the small-scale intermittency were all inhibited by the viscoelastic effects in the FHIT of the polymer solution. However, the scaling law in a fashion of extended self-similarity for the FHIT of the polymer solution, within the presently simulated range of Weissenberg numbers, had no distinct differences compared with that of the Newtonian fluid case.

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