arXiv subjects

Jens Harting

Publications and source records attributed to Jens Harting.

At least 73 records · Page 4Linked to original sources

arXiv2020

Regimes of motion of magnetocapillary swimmers

The dynamics of a triangular magnetocapillary swimmer is studied using the lattice Boltzmann method. Performing extensive numerical simulations taking into account the coupled dynamics of the fluid-fluid interface and of magnetic particles floating on it and driven by external magnetic fields we identify several regimes of the swimmer motion. In the regime of high frequencies the swimmer's maximum velocity is centered around the particle's inverse coasting time. Modifying the ratio of surface tension and magnetic forces allows to study the swimmer propagation in the regime of significantly lower frequencies mainly defined by the strength of the magnetocapillary potential. Finally, introducing a constant magnetic contribution in each of the particles in addition to their magnetic moment induced by external fields leads to another regime characterised by strong in-plane swimmer reorientations that resemble experimental observations.

cond-mat.soft↗

arXiv2020

Structure and rheology of suspensions of spherical strain-hardening capsules

We investigate the rheology of strain-hardening spherical capsules, from the dilute to the concentrated regime under a confined shear flow using three-dimensional numerical simulations. We consider the effect of capillary number, volume fraction and membrane inextensibility on the particle deformation and on the effective suspension viscosity and normal stress differences of the suspension. The suspension displays a shear-thinning behaviour which is a characteristic of soft particles such as emulsion droplets, vesicles, strain-softening capsules, and red blood cells. We find that the membrane inextensibility plays a significant role on the rheology and can almost suppress the shear-thinning. For concentrated suspensions a non-monotonic dependence of the normal stress differences on the membrane inextensibility is observed, reflecting a similar behaviour in the particle shape. The effective suspension viscosity, instead, grows and eventually saturates, for very large inextensibilities, approaching the solid particle limit. In essence, our results reveal that strain-hardening capsules share rheological features with both soft and solid particles depending on the ratio of the area dilatation to shear elastic modulus. Furthermore, the suspension viscosity exhibits a universal behaviour for the parameter space defined by the capillary number and the membrane inextensibility, when introducing the particle geometrical changes at the steady-state in the definition of the volume fraction.

physics.flu-dyn↗

arXiv2020

Inertial migration of oblate spheroids in a plane channel

We discuss an inertial migration of oblate spheroids in a plane channel, where steady laminar flow is generated by a pressure gradient. Our lattice Boltzmann simulations show that spheroids orient in the flow, so that their minor axis coincides with the vorticity direction (a log-rolling motion). Interestingly, for spheroids of moderate aspect ratios, the equilibrium positions relative to the channel walls depend only on their equatorial radius $a$. By analysing the inertial lift force we argue that this force is proportional to $a^3b$, where $b$ is the polar radius, and conclude that the dimensionless lift coefficient of the oblate spheroid does not depend on $b$, and is equal to that of the sphere of radius $a$.

physics.flu-dyn↗

arXiv2020

Capillary interactions between soft capsules protruding through thin fluid films

When a suspension dries, the suspending fluid evaporates, leaving behind a dry film composed of the suspended particles. During the final stages of drying, the height of the fluid film on the substrate drops below the particle size, inducing local interface deformations that lead to strong capillary interactions among the particles. Although capillary interactions between rigid particles are well studied, much is still to be understood about the behaviour of soft particles and the role of their softness during the final stages of film drying. Here, we use our recently-introduced numerical method that couples a fluid described using the lattice Boltzmann approach to a finite element description of deformable objects to investigate the drying process of a film with suspended soft particles. Our measured menisci deformations and lateral capillary forces, which agree well with previous theoretical and experimental works in case of rigid particles, show the deformations become smaller with increasing particles softness, resulting in weaker lateral interaction forces. At large interparticle distances, the force approaches that of rigid particles. Finally, we investigate the time dependent formation of particle clusters at the late stages of the film drying.

cond-mat.soft↗

arXiv2020

Equilibrium orientation and adsorption of an ellipsoidal Janus particle at a fluid-fluid interface

We investigate the equilibrium orientation and adsorption process of a single, ellipsoidal Janus particle at a fluid-fluid interface. The particle surface comprises equally sized parts that are hydrophobic or hydrophilic. We present free energy models to predict the equilibrium orientation and compare the theoretical predictions with lattice Boltzmann simulations. We find that the deformation of the fluid interface strongly influences the equilibrium orientation of the Janus ellipsoid. The adsorption process of the Janus ellipsoid can lead to different final orientations determined by the interplay of particle aspect ratio and particle wettablity contrast.

cond-mat.soft↗

arXiv2020

The Scallop Theorem and Swimming at the Mesoscale

By synergistically combining modeling, simulation and experiments, we show that there exists a regime of self-propulsion in which the inertia in the fluid dynamics can be separated from that of the swimmer. This is demonstrated by the motion of an asymmetric dumbbell that, despite deforming in a reciprocal fashion, self-propagates in a fluid due to a non-reciprocal Stokesian flow field. The latter arises from the difference in the coasting times of the two constitutive beads. This asymmetry acts as a second degree of freedom, recovering the scallop theorem at the mesoscopic scale.

physics.flu-dyn↗

arXiv2020

Desorption energy of soft particles from a fluid interface

The efficiency of soft particles to stabilize emulsions is examined by measuring their desorption free energy, i.e., the mechanical work required to detach the particle from a fluid interface. Here, we consider rubber-like elastic as well as microgel particles, using coarse-grained molecular dynamics simulations. The energy of desorption is computed for two and three-dimensional configurations by means of the mean thermodynamic integration method. It is shown that the softness affects the particle-interface binding in two opposing directions as compared to rigid particles. On the one hand, a soft particle spreads at the interface and thereby removes a larger unfavorable liquid-liquid contact area compared to rigid particles. On the other hand, softness provides the particle with an additional degree of freedom to get reshaped instead of deforming the interface, resulting in a smaller restoring force during the detachment. It is shown that the first effect prevails so that a soft spherical particle attaches to the fluid interface more strongly than rigid spheres. Finally, we consider microgel particles both in the swollen and in the collapsed state. Surprisingly, we find that the latter has a larger binding energy. All results are rationalised using thermodynamic arguments and thereby offer detailed insights into the desorption energy of soft particles from fluid interfaces.

cond-mat.soft↗

arXiv2020

Catalytic flow with a coupled Finite Difference -- Lattice Boltzmann scheme

Many catalyst devices employ flow through porous structures, which leads to a complex macroscopic mass and heat transport. To unravel the detailed dynamics of the reactive gas flow, we present an all-encompassing model, consisting of thermal lattice Boltzmann model by Kang et al., used to solve the heat and mass transport in the gas domain, coupled to a finite differences solver for the heat equation in the solid via thermal reactive boundary conditions for a consistent treatment of the reaction enthalpy. The chemical surface reactions are incorporated in a flexible fashion through flux boundary conditions at the gas-solid interface. We scrutinize the thermal FD-LBM by benchmarking the macroscopic transport in the gas domain as well as conservation of the enthalpy across the solid-gas interface. We exemplify the applicability of our model by simulating the reactive gas flow through a microporous material catalysing the so-called water-gas-shift reaction.

physics.flu-dyn↗

arXiv2020

Self-Similar Liquid Lens Coalescence

A basic feature of liquid drops is that they can merge upon contact to form a larger drop. In spite of its importance to various applications, drop coalescence on pre-wetted substrates has received little attention. Here, we experimentally and theoretically reveal the dynamics of drop coalescence on a thick layer of a low-viscosity liquid. It is shown that these so-called "liquid lenses" merge by the self-similar vertical growth of a bridge connecting the two lenses. Using a slender analysis, we derive similarity solutions corresponding to the viscous and inertial limits. Excellent agreement is found with the experiments without any adjustable parameters, capturing both the spatial and temporal structure of the flow during coalescence. Finally, we consider the crossover between the two regimes and show that all data of different lens viscosities collapse on a single curve capturing the full range of the coalescence dynamics.

physics.flu-dyn↗

arXiv2020

A phase-field model for the evaporation of thin film mixtures

The performance of solution-processed solar cells strongly depends on the geometrical structure and roughness of the photovoltaic layers formed during film drying. During the drying process, the interplay of crystallization and liquid-liquid demixing leads to the structure formation on the nano- and microscale and to the final rough film. In order to better understand how the film structure can be improved by process engineering, we aim at theoretically investigating these systems by means of phase-field simulations. We introduce an evaporation model based on the Cahn-Hilliard equation for the evolution of the fluid concentrations coupled to the Allen-Cahn equation for the liquid-vapour phase transformation. We demonstrate its ability to match the experimentally measured drying kinetics and study the impact of the parameters of our model. Furthermore, the evaporation of solvent blends and solvent-vapour annealing are investigated. The dry film roughness emerges naturally from our set of equations, as illustrated through preliminary simulations of spinodal decomposition and film drying on structured substrates.

physics.app-ph↗

arXiv2020

Role of the interplay between spinodal decomposition and crystal growth in the morphological evolution of crystalline bulk heterojunctions

The stability of organic solar cells is strongly affected by the morphology of the photoactive layers, whose separated crystalline and/or amorphous phases are kinetically quenched far from their thermodynamic equilibrium during the production process. The evolution of these structures during the lifetime of the cell remains poorly understood. In this paper, a phase-field simulation framework is proposed, handling liquid-liquid demixing and polycrystalline growth at the same time in order to investigate the evolution of crystalline immiscible binary systems. We find that initially, the nuclei trigger the spinodal decomposition, while the growing crystals quench the phase coarsening in the amorphous mixture. Conversely, the separated liquid phases guide the crystal growth along the domains of high concentration. It is also demonstrated that with a higher crystallization rate, in the final morphology, single crystals are more structured and form percolating pathways for each material with smaller lateral dimensions.

cond-mat.mtrl-sci↗

arXiv2019

Inertial migration of neutrally-buoyant particles in superhydrophobic channels

At finite Reynolds numbers particles migrate across flow streamlines to their equilibrium positions in microchannels. Such a migration is attributed to an inertial lift force, and it is well-known that the equilibrium location of neutrally-buoyant particles is determined only by their size and the Reynolds number. Here we demonstrate that the decoration of a bottom wall of the channel by superhydrophobic grooves provides additional possibilities for manipulation of neutrally-buoyant particles. It is shown that the effective anisotropic hydrodynamic slip of such a bottom wall can be readily used to alter the equilibrium positions of particles and to generate their motion transverse to the pressure gradient. These results may guide the design of novel inertial microfluidic devices for efficient sorting of neutrally-buoyant microparticles by their size.

cond-mat.soft↗

arXiv2019

Capillary assemblies in a rotating magnetic field

Small objects floating on a fluid have a tendency to aggregate due to capillary forces. This effect has been used, with the help of a magnetic induction field, to assemble submillimeter metallic spheres into a variety of structures, whose shape and size can be tuned. Under time-varying fields, these assemblies can propel themselves due to a breaking of time reversal symmetry in their adopted shapes. In this article, we study the influence of an in-plane rotation of the magnetic field on these structures. Various rotational modes have been observed with different underlying mechanisms. The magnetic properties of the particles cause them to rotate individually. Dipole-dipole interactions in the assembly can cause the whole structure to align with the field. Finally, non-reciprocal deformations can power the rotation of the assembly. Symmetry plays an important role in the dynamics, as well as the frequency and amplitude of the applied field. Understanding the interplay of these effects is essential, both to explain previous observations and to develop new functions for these assemblies.

cond-mat.soft↗

arXiv2019

Implementation of on-site velocity boundary conditions for D3Q19 lattice Boltzmann

On-site boundary conditions are often desired for lattice Boltzmann simulations of fluid flow in complex geometries such as porous media or microfluidic devices. The possibility to specify the exact position of the boundary, independent of other simulation parameters, simplifies the analysis of the system. For practical applications it should allow to freely specify the direction of the flux, and it should be straight forward to implement in three dimensions. Furthermore, especially for parallelized solvers it is of great advantage if the boundary condition can be applied locally, involving only information available on the current lattice site. We meet this need by describing in detail how to transfer the approach suggested by Zou and He to a D3Q19 lattice. The boundary condition acts locally, is independent of the details of the relaxation process during collision and contains no artificial slip. In particular, the case of an on-site no-slip boundary condition is naturally included. We test the boundary condition in several setups and confirm that it is capable to accurately model the velocity field up to second order and does not contain any numerical slip.

physics.flu-dyn↗

arXiv2019

Mesoscale simulation of soft particles with tunable contact angle in multi-component fluids

Soft particles at fluid interfaces play an important role in many aspects of our daily life, such as the food industry, paints and coatings, and medical applications. Analytical methods are not capable of describing the emergent effects of the complex dynamics of suspensions of many soft particles, whereas experiments typically either only capture bulk properties or require invasive methods. Computational methods are therefore a great tool to complement experimental work. However, an efficient and versatile numerical method is needed to model dense suspensions of many soft particles. In this article we propose a method to simulate soft particles in a multi-component fluid, both at and near fluid-fluid interfaces, based on the lattice Boltzmann method, and characterize the error stemming from the fluid-structure coupling for the particle equilibrium shape when adsorbed onto a fluid-fluid interface. Furthermore, we characterize the influence of the preferential contact angle of the particle surface and the particle softness on the vertical displacement of the center of mass relative to the fluid interface. Finally, we demonstrate the capability of our model by simulating a soft capsule adsorbing onto a fluid-fluid interface with a shear flow parallel to the interface, and the covering of a droplet suspended in another fluid by soft particles with different wettability.

physics.comp-ph↗

arXiv2019

A lattice Boltzmann method for thin liquid film hydrodynamics

We propose a novel approach to the numerical simulation of thin film flows, based on the lattice Boltzmann method. We outline the basic features of the method, show in which limits the expected thin film equations are recovered and perform validation tests. The numerical scheme is applied to the viscous Rayleigh-Taylor instability of a thin film and to the spreading of a sessile drop towards its equilibrium contact angle configuration. We show that the Cox-Voinov law is satisfied, and that the effect of a tunable slip length on the substrate is correctly captured. We address, then, the problem of a droplet sliding on an inclined plane, finding that the Capillary number scales linearly with the Bond number, in agreement with experimental results. At last, we demonstrate the ability of the method to handle heterogenous and complex systems by showcasing the controlled dewetting of a thin film on a chemically structured substrate.

physics.comp-ph↗

arXiv2019

A general perturbative approach for bead-based microswimmers reveals rich self-propulsion phenomena

Studies of model microswimmers have significantly contributed to the understanding of the principles of self-propulsion we have today. However, only a small number of microswimmer types have been amenable to analytic modeling, and further development of such approaches is necessary to identify the key features of these active systems. Here we present a general perturbative calculation scheme for swimmers composed of beads interacting by harmonic potentials, driven by an arbitrary force protocol. The hydrodynamic interactions are treated using the Oseen and Rotne-Pragner approximations. We validate our approach by using 3 bead assemblies and comparing the results with the numerically obtained full-solutions of the governing equations of motion, as well as with the existing analytic models for a linear and a triangular swimmer geometries. While recovering the relation between the force and swimming velocity, our detailed analysis and the controlled level of approximation allow us to find qualitative differences already in the far field flow of the devices. Consequently, we are able to identify a behavior of the swimmer that is richer than predicted in previous models. Given its generality, the framework can be applied to any swimmer geometry, driving protocol and beads interactions, as well as in many swimmers problems.

cond-mat.soft↗

arXiv2019

Strict equivalence between Maxwell-Stefan and fast-mode theory for multicomponent polymer mixtures

The applicability of theories describing the kinetic evolution of fluid mixtures depends on the underlying physical assumptions. The Maxwell-Stefan equations, widely used for miscible fluids, express forces depending on coupled fluxes. They need to be inverted to recover a Fickian form which is generally impossible analytically. Moreover, the concentration dependence of the diffusivities has to be modelled, e.g. by the multicomponent Darken equation. Cahn-Hilliard type equations are preferred for immiscible mixtures, whereby different assumptions on the coupling of fluxes lead to the slow-mode and fast-mode theories. For two components, these were derived from the Maxwell-Stefan theory in the past. Here, we prove that the fast-mode theory and the generalized Maxwell-Stefan theory together with the multicomponent Darken equation are strictly equivalent even for multicomponent systems with very different molecular sizes. Our findings allow to reduce the choice of a suitable theory to the most efficient algorithm for solving the underlying equations.

physics.chem-ph↗