The structure and spatial statistical properties of amorphous ellipsoid assemblies have profound scientific and industrial significance in many systems, from cell assays to granular materials. This paper uses a fundamental theoretical relationship for mixture distributions to explain the observations of an extensive X-ray computed tomography study of granular ellipsoidal packings. We study a size-bi-disperse mixture of two types of ellipsoids of revolutions that have the same aspect ratio of ≈ 0.57 and differ in size, by about 10% in linear dimension, and compare these to mono-disperse systems of ellipsoids with the same aspect ratio. Jammed configurations with a range of packing densities are achieved by employing different tapping protocols. We numerically interrogate the final packing configurations by analyses of the local packing fraction distributions calculated from the Voronoi diagrams. Our main finding is that the bi-disperse ellipsoidal packings studied here can be interpreted as a mixture of two uncorrelated mono-disperse packings, insensitive to the compaction protocol. Our results are consolidated by showing that the local packing fraction shows no correlation beyond their first shell of neighbours in the binary mixtures. We propose a model of uncorrelated binary mixture distribution that describes the observed experimental data with high accuracy. This analysis framework will enable future studies to test whether the observed mean-field behaviour is specific to the particular granular system or the specific parameter values studied here or if it is observed more broadly in other bi-disperse non-spherical particle systems.
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http://dx.doi.org/10.1039/d2sm00922f | DOI Listing |
ACS Nano
January 2025
Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.
Block copolymers (BCPs) can form nanoparticles having different morphologies that can be used as photonic nanocrystals and are a platform for drug delivery, sensors, and catalysis. In particular, BCP nanoparticles having disk-like shape have been recently discovered. Such nanodisks can be used as the next-generation antitumor drug delivery carriers; however, the applicability of the existing nanodisks is limited due to their poor or unknown ability to respond to external stimuli.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
School of Physics and Astronomy, The University of Edinburgh, Peter Guthrie Tait Road, Edinburgh EH9 3FD, UK; Department of Physics, University of Gothenburg, SE-41296 Gothenburg, Sweden; University of Münster, Institute of Physical Chemistry, Corrensstr. 28/30, 48149 Münster, Germany. Electronic address:
Hypothesis: Ellipsoidal particles confined at liquid interfaces exhibit complex self-assembly due to quadrupolar capillary interactions, favouring either tip-to-tip or side-to-side configurations. However, predicting and controlling which structure forms remains challenging. We hypothesize that introducing a polymer-based soft shell around the particles will modulate these capillary interactions, providing a means to tune the preferred self-assembly configuration based on particle geometry and shell properties.
View Article and Find Full Text PDFLangmuir
December 2024
Department of Biomedical and Chemical Engineering and the Bioinspired Institute, Syracuse University, Syracuse, New York 13244, United States.
Copolymer nanovesicles are used extensively in chemical processes and biomedical applications in which they are subjected to dynamic flow environments. Flow-induced vesicle deformation, fragmentation, and reorganization modify the energetic (e.g.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
December 2024
Institute of Physical Chemistry, Rheinisch-Westfälische Technische Hochschule Aachen University, Aachen 52074, Germany.
The adsorption of ellipsoidal colloidal particles on liquid interfaces induces interfacial deformation, resulting in anisotropic interface-mediated interactions and the formation of superstructures. Soft prolate-shaped microgels at the air-water interface offer an ideal model for studying spontaneous capillary-driven self-assembly due to their tunable aspect ratio, controlled functionality, and softness. These microgels consist of a polystyrene core surrounded by a cross-linked, fluorescently labeled poly([Formula: see text]-isopropylmethylacrylamide) shell.
View Article and Find Full Text PDFSoft Matter
January 2025
Shanghai Key Laboratory of Advanced Polymeric Materials, Key Laboratory for Ultrafine Materials of Ministry of Education, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China.
The self-assembly behaviors of rod-coil asymmetric diblock molecular brushes (ADMBs) bearing responsive side chains in a selective solvent are investigated dissipative particle dynamics simulations. By systematically varying the polymerization degree, copolymer concentration, and side chain length, several morphological phase diagrams were constructed. ADMB assemblies exhibited a rich variety of morphologies, including cylindrical micelles, spherical micelles, nanowires, polyhedral micelles, ellipsoid micelles, and large compound micelles.
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