Binary pusher–puller mixtures of active microswimmers and their collective behaviour

ABSTRACT

Microswimmers are active particles of microscopic size that self-propel by setting the surrounding fluid into motion. According to the kind of far-field fluid flow that they induce, they are classified into pushers and pullers. Many studies have explored similarities and differences between suspensions of either pushers or pullers, but the behaviour of mixtures of the two is still to be investigated. Here, we rely on a minimal discrete microswimmer model, particle-resolved, including hydrodynamic interactions, to examine the orientational ordering in such binary pusher–puller mixtures. In agreement with existing literature, we find that our monodisperse suspensions of pushers do not show alignment, whereas those of solely pullers spontaneously develop ordered collective motion. By continuously varying the composition of the binary mixtures, starting from pure puller systems, we find that ordered collective motion is largely maintained up to pusher–puller composition ratios of about 1:2. Surprisingly, pushers when surrounded by a majority of pullers are more tightly aligned than indicated by the average overall orientational order in the system. Our study outlines how orientational order can be tuned in active microswimmer suspensions to a requested degree by doping with other species.     

DC conductivity of a suspension of insulating particles with internal rotation

We analyse the consequences of Quincke rotation on the conductivity of a suspension. Quincke rotation refers to the spontaneous rotation of insulating particles dispersed in a slightly conducting liquid and subject to a high DC electric field: above a critical field, each particle rotates continuously around itself with an axis pointing in any direction perpendicular to the DC field. When the suspension is subject to an electric field lower than the threshold one, the presence of insulating particles in the host liquid decreases the bulk conductivity since the particles form obstacles to ion migration. But for electric fields higher than the critical one, the particles rotate and facilitate ion migration: the effective conductivity of the suspension is increased. We provide a theoretical analysis of the impact of Quincke rotation on the apparent conductivity of a suspension and we present experimental results obtained with a suspension of PMMA particles dispersed in weakly conducting liquids.     

Identification of flow mechanisms for a soft crystal

We study the behavior under flow of soft spherical micelles forming a fcc phase at high volume fraction. Due to the size (300 ?) of the elementary objects, the structure can be investigated through X-rays and neutron scattering, at rest and under flow in a Couette cell. Using scattering in two perpendicular directions, different mechanisms of flow are identified. At intermediate shear (around 100 s^-1) the system exhibits the so called layer sliding mechanism where two dimensional hexagonal compact planes of spheres align themselves with the Couette cell walls. At lower shear rate, the fcc structure is locally preserved, and the flow is mediated by defects between crystallites. At high shear rate, we observe the melting of the structure and a liquid-like structure factor. Moreover, we were able to use the existence of the layer sliding regime to generate a fcc monocrystal by annealing the satcking faults between the decorrelated planes created by the layer sliding. Received: 7 July 1997 / Received in final form: 16 January 1998 / Accepted: 5 March 1998     

Bending of charged flexible membranes due to the presence of macroions

We investigate the bending of flexible charged membranes due to the presence of rigid rodlike macroions in the framework of the Debye-Hückel approximation. When the macroions are fixed in space at some distance from the bilayer the membrane bends towards them; we calculate the exact deformation profile. On the other hand a macroion which is adsorbed on the membrane causes a deflection of the bilayer. Finally, we consider swollen lamellar polyanion/charged-lipid complexes where the macroions are intercalated between charged lipid bilayers. We predict the occurrence of a double adsorption (pinching effect) of the macroion for sufficiently flexible membranes. Received: 9 February 1998 / Revised: 9 June 1998 / Accepted: 2 July 1998     

ELECTROSTATICALLY SUPPORTED MIXING OF FINE GRAINED PARTICLES

The processing of fine-grained particles with diameters between 1 and 10 microns is difficult due to strong van-der-Waals attraction forces. In order to improve the handling properties, the fine-grained particles, i.e. host-particles,are coated with various nanoparticles, i.e. guest-particles. The mixing of fine-grained powders is influenced by particle-particle interactions. If these forces are distinctively used, both interactive and ordered mixtures can be produced.These particle mixtures consist of composite-particles that have new physical properties. These modified properties d epend strongly on the coating process, the diameter- and mass-relationship of the guest- and the host-particles. The properties of the composite-particles can systematically be adjusted to the requirements of industrial applications. For example, a laboratory bubbling fluidized bed can be used to describe the conveying behavior of the functionalized host-particles. Applications for the functionalized particles are in the pharmaceutical and the powder coating industries,e.g. enhanced dry powder inhalers and thin lacquer films. The present research compares three different mixing/coating processes. The composite-particles are characterized by TEM, SEM and with their fluidization characteristics. The coating process itself is monitored by the electrostatic charge of the particles.     

Rheology of concentrated alumina-polyelectrolyte systems

Rheological properties of concentrated alumina suspensions using a charged copolymer as the dispersant have been studied. The non-Newtonian behavior of these fluids was characterized and correlated to potential measurements and sedimentation column data, obtained with these dispersions. As a result, a clear relationship between dispersion stability and pseudoplastic/dilatant rheological behavior was established.     

Rheological properties of suspensions of polyethylene-coated aluminum nanoparticles

Ultrafine aluminum powder was identified as very promising fuels for novel energetic materials formulations. However, the large specific surface area of this powder facilitates its oxidation and greatly reduces its shelf life. Therefore, different coating processes were proposed to solve this problem. The rheology of viscous suspensions of nanoparticles still remains poorly understood and the effect of the coating of such particles on the flow behavior is even more difficult to assess. We have studied the rheology of ultrafine aluminum suspensions in three low molecular weight polymers of different viscosities: a hydroxy-terminated polybutadiene, a polypropylene glycol, and a polysiloxane. The nanosize aluminum powder was previously coated by a thin layer of high-density polyethylene using an in situ polymerization process. The rheological characterization of the suspensions was conducted by the means of steady and oscillatory shear flow measurements for noncoated and coated particles. The effect of the coating process on the rheology of the suspensions is discussed in terms of the interactions between the particles and the suspending fluids.     

Rheology of physically evolving suspensions

The objective of this work was to investigate the modeling of the whole dynamic rheological behavior of physically evolving suspensions (e.g., polyvinyl chloride plastisols). The evolutions of the complex viscosity with time (isothermal) and with temperature (non-isothermal) were analyzed. To understand the physically involved phenomena, the determination of relationships between the solid volume fraction evolution and the rheological behavior was investigated. Firstly, the evolution of the volume fraction in relation with the variation of radii particle suspensions using a modified Avrami equation was determined. Actually, the rheological study of this physically evolving system is far too complicated due to the many factors involved in the evolving process. Consequently, a phenomenological law using Carreau–Yasuda equation and percolation laws combined with the evolution of the solid volume fraction is investigated to obtain the modeling of the whole dynamic rheological behavior at any frequency and temperature.     

Peculiar features in the rheological behavior of electrorheological suspensions

Studies have been made of concentrated (up to 60%) diatomite suspensions in transformer oil, the structure and theological properties of which depend on an applied electric field. Studies have been conducted of steady-state and transient regimes of straining involving continuous and periodic shear. The structure in such suspensions is formed in the presence of an electric field of 10^–3 –10² duration. The suspensions under continuous stationary strain behave as non-Newtonian fluids with a yield stress dependent on electric intensity. Under periodic deformation conditions the test suspensions exhibit elasticity which abruptly diminishes with increasing deformation amplitude.     

From Colloidal Dispersions of Zeolite Monolayers to Effective Solid Catalysts in Transformations of Bulky Organic Molecules: Role of Freeze-Drying and Dialysis

We investigated the properties and catalytic activity of zeolites with MWW topology obtained by unprecedented liquid exfoliation of the MCM-56 zeolite into solutions of monolayers and isolation/reassembly of the dispersed layers by various methods, with optional purification by dialysis or ammonium exchange. The layers were recovered by flocculation with alcohol or ammonium nitrate and freeze-drying. Flocculation alone, even with ammonium nitrate, did not ensure removal of residual sodium cations resulting in catalysts with low activity. Dialysis of the solutions with dispersed monolayers proved to be efficient in removing sodium cations and preserving microporosity. The monolayers were also isolated as solids by freeze-drying. The highest BET area and pore volume obtained with the freeze-dried sample confirmed lyophilization efficiency in preserving layer structure. The applied test reaction, Friedel–Crafts alkylation of mesitylene, showed high benzyl alcohol conversion due to increased concentration of accessible acid centers caused by the presence of secondary mesoporosity. The applied treatments did not change the acid strength of the external acid sites, which are the most important ones for converting bulky organic molecules. Zeolite acidity was not degraded in the course of exfoliation into monolayers, showing the potential of such colloid dispersions for the formation of active catalysts.