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Authors = Eugene M. Terentjev

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28 pages, 2639 KiB  
Review
Theory of Semiflexible Filaments and Networks
by Fanlong Meng and Eugene M. Terentjev
Polymers 2017, 9(2), 52; https://doi.org/10.3390/polym9020052 - 5 Feb 2017
Cited by 54 | Viewed by 9570
Abstract
We briefly review the recent developments in the theory of individual semiflexible filaments, and of a crosslinked network of such filaments, both permanent and transient. Starting from the free energy of an individual semiflexible chain, models on its force-extension relation and other mechanical [...] Read more.
We briefly review the recent developments in the theory of individual semiflexible filaments, and of a crosslinked network of such filaments, both permanent and transient. Starting from the free energy of an individual semiflexible chain, models on its force-extension relation and other mechanical properties such as Euler buckling are discussed. For a permanently crosslinked network of filaments, theories on how the network responds to deformation are provided, with a focus on continuum approaches. Characteristic features of filament networks, such as nonlinear stress-strain relation, negative normal stress, tensegrity, and marginal stability are discussed. In the new area of transient filament network, where the crosslinks can be dynamically broken and re-formed, we show some recent attempts for understanding the dynamics of the crosslinks, and the related rheological properties, such as stress relaxation, yield stress and plasticity. Full article
(This article belongs to the Special Issue Semiflexible Polymers)
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14 pages, 1010 KiB  
Article
Transient Network at Large Deformations: Elastic–Plastic Transition and Necking Instability
by Fanlong Meng and Eugene M. Terentjev
Polymers 2016, 8(4), 108; https://doi.org/10.3390/polym8040108 - 24 Mar 2016
Cited by 25 | Viewed by 8099
Abstract
We theoretically investigate the mechanical response of a transient network, which is characterised by dynamically breaking and re-forming crosslinks, and accounts for the finite chain extensibility (thus permitting the large deformations to be described). We build the general theory that incorporates the widely [...] Read more.
We theoretically investigate the mechanical response of a transient network, which is characterised by dynamically breaking and re-forming crosslinks, and accounts for the finite chain extensibility (thus permitting the large deformations to be described). We build the general theory that incorporates the widely accepted empirical model of hyper-elasticity at large deformations (the Gent model) and naturally includes the microscopic behavior of transient crosslinks under the local tension applied to them. The full analytical expression for the elastic energy, or equivalently, the constitutive relation for arbitrary deformation is derived, and then the example of uniaxial tensile strain is focused on. In this case, we show that the mechanical response depends on the ratio of the imposed strain rate and the breakage rate of the crosslink: the system flows plastically (over a yield point) when the strain rate is much smaller than the breakage rate, while it remains elastic when the strain rate is much larger than the breakage rate. There is a broad range of this transition when the elastic and plastic regions of the sample coexist, and a resulting necking instability occurs. As a generalisation, we also consider a dual transient network, with two components penetrating each other, each having its own microscopic crosslink dynamics. The two networks add their local forces and share the deformation; we find that the network with a lower breakage rate determines the global deformation of the system. Full article
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25 pages, 821 KiB  
Review
Nanoparticle-Liquid Crystalline Elastomer Composites
by Yan Ji, Jean E. Marshall and Eugene M. Terentjev
Polymers 2012, 4(1), 316-340; https://doi.org/10.3390/polym4010316 - 30 Jan 2012
Cited by 78 | Viewed by 13801
Abstract
Liquid crystalline elastomers (LCEs) exhibit a number of remarkable physical effects, including a uniquely high-stroke reversible mechanical actuation triggered by external stimuli. Fundamentally, all such stimuli affect the degree of liquid crystalline order in the polymer chains cross-linked into an elastic network. Heat [...] Read more.
Liquid crystalline elastomers (LCEs) exhibit a number of remarkable physical effects, including a uniquely high-stroke reversible mechanical actuation triggered by external stimuli. Fundamentally, all such stimuli affect the degree of liquid crystalline order in the polymer chains cross-linked into an elastic network. Heat and the resulting thermal actuation act by promoting entropic disorder, as does the addition of solvents. Photo-isomerization is another mechanism of actuation, reducing the orientational order by diminishing the fraction of active rod-like mesogenic units, mostly studied for azobenzene derivatives incorporated into the LCE composition. Embedding nanoparticles provides a new, promising strategy to add functionality to LCEs and ultimately enhance their performance as sensors and actuators. The motivation for the combination of nanoparticles with LCEs is to provide better-controlled actuation stimuli, such as electric and magnetic fields, and broad-spectrum light, by selecting and configuring the appropriate nanoparticles in the LCE matrix. Here we give an overview of recent advances in this area with a focus on preparation, physical properties and actuation performance of the resultant nanocomposites. Full article
(This article belongs to the Special Issue Liquid Crystalline Polymers)
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21 pages, 1264 KiB  
Review
Dispersion of Carbon Nanotubes: Mixing, Sonication, Stabilization, and Composite Properties
by Yan Yan Huang and Eugene M. Terentjev
Polymers 2012, 4(1), 275-295; https://doi.org/10.3390/polym4010275 - 23 Jan 2012
Cited by 573 | Viewed by 36013
Abstract
Advances in functionality and reliability of carbon nanotube (CNT) composite materials require careful formulation of processing methods to ultimately realize the desired properties. To date, controlled dispersion of CNTs in a solution or a composite matrix remains a challenge, due to the strong [...] Read more.
Advances in functionality and reliability of carbon nanotube (CNT) composite materials require careful formulation of processing methods to ultimately realize the desired properties. To date, controlled dispersion of CNTs in a solution or a composite matrix remains a challenge, due to the strong van der Waals binding energies associated with the CNT aggregates. There is also insufficiently defined correlation between the microstructure and the physical properties of the composite. Here, we offer a review of the dispersion processes of pristine (non-covalently functionalized) CNTs in a solvent or a polymer solution. We summarize and adapt relevant theoretical analysis to guide the dispersion design and selection, from the processes of mixing/sonication, to the application of surfactants for stabilization, to the final testing of composite properties. The same approaches are expected to be also applicable to the fabrication of other composite materials involving homogeneously dispersed nanoparticles. Full article
(This article belongs to the Special Issue Carbon Nanotubes: Synthesis, Characterization and Applications)
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