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Solvent-Dependent Dynamics of Cellulose Nanocrystals in Process-Relevant Flow Fields

Wang, Ruifu (author)
Department of Chemistry, Stony Brook University, Stony Brook, New York 11794-3400, United States
He, HongRui (author)
Department of Chemistry, Stony Brook University, Stony Brook, New York 11794-3400, United States
Tian, Jiajun (author)
Department of Chemistry, Stony Brook University, Stony Brook, New York 11794-3400, United States
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Chodankar, Shirish (author)
National Synchrotron Light Source II, Brookhaven National Laboratory, Upton, New York 11793-5000, United States
Hsiao, Benjamin S. (author)
Department of Chemistry, Stony Brook University, Stony Brook, New York 11794-3400, United States
Rosén, Tomas, 1985- (author)
KTH,Wallenberg Wood Science Center,Fiberprocesser
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 (creator_code:org_t)
American Chemical Society (ACS), 2024
2024
English.
In: Langmuir. - : American Chemical Society (ACS). - 0743-7463 .- 1520-5827. ; 40:25, s. 13319-13329
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Flow-assisted alignment of anisotropic nanoparticles is a promising route for the bottom-up assembly of advanced materials with tunable properties. While aligning processes could be optimized by controlling factors such as solvent viscosity, flow deformation, and the structure of the particles themselves, it is necessary to understand the relationship between these factors and their effect on the final orientation. In this study, we investigated the flow of surface-charged cellulose nanocrystals (CNCs) with the shape of a rigid rod dispersed in water and propylene glycol (PG) in an isotropic tactoid state. In situ scanning small-angle X-ray scattering (SAXS) and rheo-optical flow-stop experiments were used to quantify the dynamics, orientation, and structure of the assigned system at the nanometer scale. The effects of both shear and extensional flow fields were revealed in a single experiment by using a flow-focusing channel geometry, which was used as a model flow for nanomaterial assembly. Due to the higher solvent viscosity, CNCs in PG showed much slower Brownian dynamics than CNCs in water and thus could be aligned at lower deformation rates. Moreover, CNCs in PG also formed a characteristic tactoid structure but with less ordering than CNCs in water owing to weaker electrostatic interactions. The results indicate that CNCs in water stay assembled in the mesoscale structure at moderate deformation rates but are broken up at higher flow rates, enhancing rotary diffusion and leading to lower overall alignment. Albeit being a study of cellulose nanoparticles, the fundamental interplay between imposed flow fields, Brownian motion, and electrostatic interactions likely apply to many other anisotropic colloidal systems.

Subject headings

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)
NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)
NATURVETENSKAP  -- Fysik -- Den kondenserade materiens fysik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences -- Condensed Matter Physics (hsv//eng)

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