arXiv subjects

Natsuhiko Yoshinaga

Publications and source records attributed to Natsuhiko Yoshinaga.

30 records · Page 2Linked to original sources

arXiv2013

Rotational motion of a droplet induced by interfacial tension

Spontaneous rotation of a droplet induced by the Marangoni flow is analyzed in a two-dimensional system. The droplet with the small particle which supplies a surfactant at the interface is considered. We calculated flow field around the droplet using Stokes equation and found that advective nonlinearity breaks symmetry for rotation. Theoretical calculation indicates that the droplet spontaneously rotates when the radius of the droplet is an appropriate size. The theoretical results were validated through comparison with the experiments.

cond-mat.soft↗

arXiv2012

Drift instability in the motion of a fluid droplet with a chemically reactive surface driven by Marangoni flow

We theoretically derive the amplitude equations for a self-propelled droplet driven by Marangoni flow. As advective flow driven by surface tension gradient is enhanced, the stationary state becomes unstable and the droplet starts to move. The velocity of the droplet is determined from a cubic nonlinear term in the amplitude equations. The obtained critical point and the characteristic velocity are well supported by numerical simulations.

cond-mat.soft↗

arXiv2012

Contraction of cross-linked actomyosin bundles

Cross-linked actomyosin bundles retract when severed in vivo by laser ablation, or when isolated from the cell and micromanipulated in vitro in the presence of ATP. We identify the time scale for contraction as a viscoelastic time tau, where the viscosity is due to (internal) protein friction. We obtain an estimate of the order of magnitude of the contraction time tau ~ 10-100 s, consistent with available experimental data for circumferential microfilament bundles and stress fibers. Our results are supported by an exactly solvable, hydrodynamic model of a retracting bundle as a cylinder of isotropic, active matter, from which the order of magnitude of the active stress is estimated.

q-bio.QM↗

arXiv2012

Self-propelled motion of a fluid droplet under chemical reaction

We study self-propelled dynamics of a droplet due to a Marangoni effect and chemical reactions in a binary fluid with a dilute third component of chemical product which affects the interfacial energy of a droplet. The equation for the migration velocity of the center of mass of a droplet is derived in the limit of an infinitesimally thin inter- face. We found that there is a bifurcation from a motionless state to a propagating state of droplet by changing the strength of the Marangoni effect.

nlin.PS↗

arXiv2011

Spontaneous motion of a droplet coupled with a chemical wave

We propose a novel framework for the spontaneous motion of a droplet coupled with internal dynamic patterns generated in a reaction-diffusion system. The spatio-temporal order of the chemical reaction gives rise to inhomogeneous surface tension and results in self-propulsion driven by the surrounding flow due to the Marangoni effect. Numerical calculations of internal patterns together with theoretical results of the flow fields at low Reynolds number well reproduces the experimental results obtained using a droplet of Belousov-Zhabotinsky (BZ) reaction medium.

cond-mat.soft↗

arXiv2010

Active Motion of Janus Particle by Self-thermophoresis in Defocused Laser Beam

We study self-propulsion of a half-metal coated colloidal particle under laser irradiation. The motion is caused by self-thermophoresis: i.e. absorption of laser at the metal-coated side of the particle creates local temperature gradient which in turn drives the particle by thermophoresis. To clarify the mechanism, temperature distribution and a thermal slip flow field around a micro-scale Janus particle are measured for the first time. With measured temperature drop across the particle, the speed of self-propulsion is corroborated with the prediction based on accessible parameters. As an application for driving micro-machine, a micro-rotor heat engine is demonstrated.

cond-mat.soft↗

arXiv2009

Manipulation of Colloids by Nonequilibrium Depletion Force in Temperature Gradient

The non-equilibrium distribution of colloids in a polymer solution under a temperature gradient is studied experimentally. A slight increase of local temperature by a focused laser drives the colloids towards the hot region, resulting in the trapping of the colloids irrespective of their own thermophoretic properties. An amplification of the trapped colloid density with the polymer concentration is measured, and is quantitatively explained by hydrodynamic theory. The origin of the attraction is a migration of colloids driven by a non-uniform polymer distribution sustained by the polymer's thermophoresis. These results show how to control thermophoretic properties of colloids.

cond-mat.soft↗

arXiv2009

Dynamics of Polymer Decompression: Expansion, Unfolding and Ejection

The dynamics of polymer decompression, i.e., a process from compressed, compact state to the relaxed swoll en conformation, can be formally described as a {\it nonlinear diffusion}. We discuss here two basic examples: (i) the expansion, or unfolding from a compact state, and (ii) the ejection of pressed polymer through a pore. The problem can be solved exactly for the case (i), but not for the latter. Even in such situations, a scheme called {\it uniform approximation} is shown to be useful to get a physical insight involved. Its application to the case (ii) is able to account for conflicting numerical data in a consistent way.

cond-mat.soft↗

arXiv2008

On the Adsorption of Two-State Polymers

Monte Carlo(MC) simulations produce evidence that annealed copolymers incorporating two interconverting monomers, P and H, adsorb as homopolymers with an effective adsorption energy per monomer, $ε_{eff}$, that depends on the PH equilibrium constants in the bulk and at the surface. The cross-over exponent, $Φ,$ is unmodified. The MC results on the overall PH ratio, the PH ratio at the surface and in the bulk as well as the number of adsorbed monomers are in quantitative agreement with this hypothesis and the theoretically derived $ε_{eff}$. The evidence suggests that the form of surface potential does not affect $Φ$ but does influence the PH equilibrium.

cond-mat.soft↗

arXiv2008

Folding and unfolding kinetics of a single semiflexible polymer

We theoretically investigate the kinetics of the folding transition of a single semiflexible polymer. In the folding transition, the growth rate decrease with an increase in the number of monomers in a collapsed domain, suggesting that the main contribution to dissipation is from the motion of the domain. In the unfolding transition, dynamic scaling exponents, 1/8 and 1/4, were determined for disentanglement and relaxation steps, respectively. We performed Langevin dynamics simulations to test our theory. It is found that our theory is in good agreement with simulations. We also propose the kinetics of the transitions in the presence of the hydrodynamic interaction.

cond-mat.soft↗

arXiv2007

Core-shell structures in single flexible-semiflexible block copolymers: Finding the free energy minimum for the folding transition

We investigate the folding transition of a single diblock copolymer consisting of a semiflexible and a flexible block. We obtain a {\it Saturn-shaped} core-shell conformation in the folded state, in which the flexible block forms a core and the semiflexible block wraps around it. We demonstrate two distinctive features of the core-shell structures: (i) The kinetics of the folding transition in the copolymer are significantly more efficient than those of a semiflexible homopolymer. (ii) The core-shell structure does not depend on the transition pathway.

cond-mat.soft↗

arXiv2005

Different pathways in mechanical unfolding/folding cycle of a single semiflexible polymer

Kinetics of conformational change of a semiflexible polymer under mechanical external field were investigated with Langevin dynamics simulations. It is found that a semiflexible polymer exhibits large hysteresis in mechanical folding/unfolding cycle even with a slow operation, whereas in a flexible polymer, the hysteresis almost disappears at a sufficiently slow operation. This suggests that the essential features of the structural transition of a semiflexible polymer should be interpreted at least on a two-dimensional phase space. The appearance of such large hysteresis is discussed in relation to different pathways in the loading and unloading processes. By using a minimal two-variable model, the hysteresis loop is described in terms of different pathways on the transition between two stable states.

cond-mat.soft↗