Cellulose nanofibrils and nanocrystals in confined flow: Single-particle dynamics to collective alignment revealed through scanning small-angle x-ray scattering and numerical simulations

Tomas Rosén, Ruifu Wang, Chengbo Zhan, Hongrui He, Shirish Chodankar, and Benjamin S. Hsiao
Phys. Rev. E 101, 032610 – Published 31 March 2020
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Abstract

Nanostructured materials made through flow-assisted assembly of proteinaceous or polymeric nanosized fibrillar building blocks are promising contenders for a family of high-performance biocompatible materials in a wide variety of applications. Optimization of these processes relies on improving our knowledge of the physical mechanisms from nano- to macroscale and especially understanding the alignment of elongated nanoparticles in flows. Here, we study the full projected orientation distributions of cellulose nanocrystals (CNCs) and nanofibrils (CNFs) in confined flow using scanning microbeam SAXS. For CNCs, we further compare with a simulated system of dilute Brownian ellipsoids, which agrees well at dilute concentrations. However, increasing CNC concentration to a semidilute regime results in locally arranged domains called tactoids, which aid in aligning the CNC at low shear rates, but limit alignment at higher rates. Similarly, shear alignment of CNF at semidilute conditions is also limited owing to probable bundle or flock formation of the highly entangled nanofibrils. This work provides a quantitative comparison of full projected orientation distributions of elongated nanoparticles in confined flow and provides an important stepping stone towards predicting and controlling processes to create nanostructured materials on an industrial scale.

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  • Received 7 August 2019
  • Revised 11 December 2019
  • Accepted 9 March 2020

DOI:https://doi.org/10.1103/PhysRevE.101.032610

©2020 American Physical Society

Physics Subject Headings (PhySH)

Fluid DynamicsPolymers & Soft MatterInterdisciplinary Physics

Authors & Affiliations

Tomas Rosén1,2,*, Ruifu Wang1, Chengbo Zhan1, Hongrui He1, Shirish Chodankar3, and Benjamin S. Hsiao1

  • 1Department of Chemistry, Stony Brook University, Stony Brook, New York 11794-3400, USA
  • 2Treesearch, KTH Royal Institute of Technology, 10044 Stockholm, Sweden
  • 3National Synchrotron Light Source II, Brookhaven National Laboratory, Upton, New York 11973, USA

  • *trosen@kth.se

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Issue

Vol. 101, Iss. 3 — March 2020

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