Energy, enstrophy and helicity transfers in polymeric turbulence

preprint2025arXivOpen access

Abstract

We characterise the scale-by-scale transfers of energy, enstrophy and helicity in homogeneous and isotropic polymeric turbulence using direct numerical simulations. The microscale Reynolds number is set to Reλ≈460Re_λ\approx 460, and the Deborah number De=τp/τfDe = τ_p/τ_f is varied between 1/9≤De≤91/9 \le De \le 9; τpτ_p is the polymeric relaxation time and τfτ_f is the turnover time of the largest scales of the flow. The study relies on the exact scale-by-scale budget equations (derived from the the governing model equations) for energy, enstrophy and helicity, which account for the back-reaction of the polymers on the flow. Polymers act as a sink/source in the flow, and provide alternative routes for the scale-by-scale transfers of the three quantities, whose relevance changes with DeDe. We find that polymers deplete the nonlinear energy cascade mainly at smaller scales, by weakening both the extreme forward as well as reverse local events. The new polymer-driven energy flux dominates at small scales for De≥1De \ge 1, and on average transfers energy from larger to smaller scales with localised backscatter events. Polymers weaken the stretching of vorticity with the enstrophy being mainly generated by the fluid-polymer interaction, especially when De≥1De \ge 1. Accordingly, an inspection of the small-scale flow topology shows that polymers favour events with two-dimensional state of straining, and promote/inhibit extreme extension/rotation events: in polymeric turbulence shear and planar extensional flows are more probable. The helicity injected at the largest scales shows a similar transfer process to as energy, being mainly driven by the nonlinear cascade at large scales and by the polymer-driven flux at small scales. Polymers are found to favour events that break the small-scale mirror symmetry, with the relative helicity monotonically increasing with DeDe at all scales.

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