The present invention generally relates to self-assembled structures. Specifically to interface colloidal robotic manipulators.
This section is intended to provide a background or context to the invention that is recited in the claims. The description herein may include concepts that could be pursued, but are not necessarily ones that have been previously conceived or pursued. Therefore, unless otherwise indicated herein, what is described in this section is not prior art to the description and claims in this application and is not admitted to be prior art by inclusion in this section.
Researchers in various disciplines have attempted to capture and hold motile and highly-diffusive objects such as viruses, small colloids, and bacterial. The small size of such objects, as well as the environment in which they are found has presented problems in efficient and repeatable systems and methods for transporting objects.
Current systems utilize complex laser systems to attempt to orient, position, and manipulate small objects. Optical tweezer systems have been developed to utilize light directed through an objected lens to manipulate an object in three-dimensional space.
One embodiment of the invention relates to a system for manipulating particle. The system comprises a first liquid and a second liquid that are immiscible. Magnetic microparticles dispersed at the interface of the two immiscible liquids. A magnetic source positioned to apply an alternating magnetic field to the dispersed magnetic microparticles.
One embodiment of the invention relates to a self assembling structure comprising a plurality of magnetic microparticles suspended at a liquid-liquid interface. The plurality of magnetic microparticles arranged by dipole-dipole magnetic interactions with an external magnetic field. The structure further comprises a deformation resulting in a non-symmetrical shape of the self assembled structure.
One embodiment of the invention relates to a method for magnetic manipulation of self-assembled colloidal asters comprising: suspending magnetic particles at an interface between two immiscible liquids; energizing the ferromagnetic suspension by application of a vertically positioned ac magnetic field; forming chains of magnetic particles; rocking the chains of magnetic particles by action of the ac magnetic field; deforming the interface; and generating a hydrodynamic streaming flow associated with the chains of magnetic particles.
Additional features, advantages, and embodiments of the present disclosure may be set forth from consideration of the following detailed description, drawings, and claims. Moreover, it is to be understood that both the foregoing summary of the present disclosure and the following detailed description are exemplary and intended to provide further explanation without further limiting the scope of the present disclosure claimed.
The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of necessary fee.
The foregoing and other objects, aspects, features, and advantages of the disclosure will become more apparent and better understood by referring to the following description taken in conjunction with the accompanying drawings, in which:
a-g illustrate self-assembled dynamic asters.
a-2f illustrate structure and hydrodynamic signature of asters.
a-d show magnetic ordering of asters.
a and 4b show controlled locomotion and gripper functionality of asters.
a-5d show the collection, encaging, and transport of particles by a cluster of asters.
a and 7b illustrate that colloidal crystals are possible for dc (constant) magnetic field and linear snakes are possible for ac (alternating) magnetic field. In the illustrated example, Hac=100 Oe, 50 Hz with 90 micrometer nickel spherical particles.
a-c illustrate examples where large-scale surface vortex flows are created.
a-c illustrates self-assembled pumps in accordance with the present invention.
In the following detailed description, reference is made to the accompanying drawings, which form a part hereof. In the drawings, similar symbols typically identify similar components, unless context dictates otherwise. The illustrative embodiments described in the detailed description, drawings, and claims are not meant to be limiting. Other embodiments may be utilized, and other changes may be made, without departing from the spirit or scope of the subject matter presented here. It will be readily understood that the aspects of the present disclosure, as generally described herein, and illustrated in the figures, can be arranged, substituted, combined, and designed in a wide variety of different configurations, all of which are explicitly contemplated and made part of this disclosure.
Self-assembly gives rise to materials that are far more complex than traditional metals, ceramics, and polymers with many levels of functionality, hierarchical organization, and compartmentalization. However, self-assembled materials pose a formidable challenge in that they are intrinsically complex, with organization often occurring on many nested length and time scales. It is practical to identify two major classes of self-assembling systems: static and dynamic. A static self-assembly involves systems that are at global or local equilibrium and do not dissipate energy. In a dynamic self-assembly observed out of equilibrium, the interactions responsible for the formation of structures occur only if the system actively consumes energy from an external energy source, provided, for example, by an applied field or chemical reaction. Resulting dynamic structures are not usually accessible under equilibrium conditions. Active colloidal suspensions are both promising candidates for understanding the guiding principles of dynamic self-assembly and convenient platforms for the design of new functional self-assembled structures; this is largely because of their controllability, size and diverse range of interactions.
The present invention relates to structures exhibiting self-assembly, in a specific embodiment, self assembly via a ferromagnetic colloidal suspension placed at the interface (boundary) between two immiscible liquids and energized by a uniform alternating (a.c.) magnetic field. The magnetic field is applied perpendicular to the interface between the liquids, and it provides an energy source that drives the system out of equilibrium; it also functions as a convenient knob to control the emerging architectures. In one embodiment, if the magnetic field is not strictly perpendicular to the interface, the emerging structures become asymmetric and generally drift towards container wall; the drift can be neglected if the field is vertical within several degrees
In accordance with the present invention, magnetic colloids, confined at the interface between two immiscible liquids and energized by an alternating magnetic field, form a variety of complex dynamic self-assembled structures, including localized asters and tunable array of asters. Aster is a description of the shape of the structures having a similarity with the flower aster. This embodiment of the self-assembled structure is called aster because the magnetic chains radiate from the center Amongst the striking new features of these structures are the ability to change shape and control locomotion in response to external stimuli. Asters and aster arrays are capable of performing simple manipulations capturing transporting, and positioning particles. Embodiments of the present invention give new insights into the engineering of “smart” synthetic materials by means of dynamic self-assembly and new design concepts for “soft robotics”.
The systems and method of the present invention provide for a remarkable diversity of dynamic self-assembled structures. In one embodiment, shown in
In one embodiment, dynamic self-assembly is caused by the interactions between ferromagnetic particles responding to an external periodic magnetic field and both self-induced interface deformations and hydrodynamic flows in the bulk of the liquids. In one embodiment, an alternating current magnetic field is used and usage of a direct current magnetic field forms colloidal crystals instead of the described structures. The surface deformations are not imposed, they are an outcome of the ac magnetic field acting on magnetic particles. A short-range magnetic order, governed by dipole-dipole magnetic interactions between the particles, promotes the formation of chains. These chains, rocking periodically in a response to an a.c. vertical magnetic field (if the field is not vertical, the structures may drift), deform the interface and lead to a resonant excitation of interfacial waves with the wavelength determined by the corresponding dispersion relation, equation (1) set forth below.
In addition, the periodic oscillations of the interface (of the two liquids) at the frequency of the applied magnetic field f excite quasi-static hydrodynamic streaming flows owing to the non-negligible interia of the fluids (the typical Reynolds number for the asters is of the order of 10). These streaming flows are a manifestation of well-known Rayeigh or acoustic streaming phenomenon for oscillatory fluid motions. The waves and self-induced streaming flows provide a necessary feedback mechanism that leads to the formation of asters and arrays. Self-induced flow resulted in a long-range attraction between magnetic chains and caused concentration. Because the magnetic forces (dipolar) and self-induced hydrodynamic flows (quadrupole) have fundamentally different symmetry, the resulting patterns are very different from those arising from the magnetic forces alone. Consequently, the inter-aster distances (lattice constant) in array of asters defined by the dispersion relation for the waves at the interface between two liquids,
Here, the wavenumber, is the angular frequency, ρ1 and ρ2 are the densities of the two liquids (ρ1>ρ2), and g and σ12 are the gravitational acceleration and interfacial tension respectively. The array's lattice constant as well as the wavelength of linear snake-like objects accurately approximates the dispersion relation (
The arrangement of chains within an aster is governed by the self-induced hydrodynamic streaming flows and dipole-dipole repulsion of chains. In contrast to magnetic snakes observed at liquid-air interfaces, the presence of the top liquid drastically changes the overall force balance and, correspondingly, the outcome of a dynamic self-assembly. Specifically, an excited circular wave leads to the formation of radial ordering of the magnetic chains. The chains decorate the slopes of the self-induced circular standing wave. A schematic view of an aster is shown in
The hydrodynamic signature of asters has been further analyzed by a particle image velocimetry (as further described in the examples below). Asters generate large-scale three-dimensional (3D) toroidal streaming flows in both liquids, as shown schematically in
In one embodiment, the asters are composed of ferromagnetically ordered chains of microparticles decorating circular interfacial wave. This arrangement implies two permissible magnetic configurations, aster and anti-aster (flavou): magnetic moments pointing inwards, towards the centre of the aster (
On removal of the in-plane field, the structures close down and recover their initial shapes. Asters and anti-asters, when located close to each other, can exchange particles owing dipole-dipole attractive forces between their chains. If both asters have a similar size, a dynamic equilibrium is established: particles in the contact region constantly change their ‘ownership’, (
The aster's shape change in a response to an applied in-plane magnetic field results in a surprising phenomenon: controlled locomotion. The aster's shape is determined by a fine balance between particle interactions and self-induced hydrodynamic flows: for an axi-symmetric aster the flow is also symmetric and no motion of the aster's center-of-mass occurs. Thus, the deformation of the aster's shape deformation by an external field inevitably leads to the breakdown of the axial symmetry of the hydrodynamic flow and the onset of self-propulsion. Direction of locomotion can be controlled by the direction of magnetic field. A change in the orientation of the magnetic field will produce change in two-dimensional motion of a structure, such as an aster. Reversing the direction of magnetic field reverses the direction of locomotion
The propulsion speed depends on the aster's asymmetry (i.e. deformation), controlled in turn by an applied in-plane magnetic field (
The ability to control the opening of asters and their, speed and direction of propulsion allows one to manipulate non-magnetic particles at the interface. Opening of an aster is controlled by the magnitude of in-plane magnetic field, see
Self-assembled arrays and clusters of asters provide additional functionality not available from a single aster. An array membrane can collect, encage, and transport particles of interest in the interstitial space between the individual asters.
a and 7b illustrate that colloidal crystals and snakes are possible. In the illustrated example, Hac=100 Oe, 50 Hz with 90 micrometer nickel spherical particles.
a-c illustrate examples where large-scale surface vortex flows are created.
In one embodiment, the structure may be a pump.
In one embodiment, the structure may exhibit movement.
In one embodiment, the structure may be formed under water. The structure is formed at the liquid-liquid interface, such as oil and water. A reduced density contrast results in a reduction in size.
Nickel spherical microparticles with an average size of 90 μm (Alfa Aesar Company) were used in the experiments. Microparticles were dispersed at the interface between two immiscible liquids. The bottom liquid was a 5 cm deep saturated solution of Na2SO4 in water, with density ρ=1,136 kgm-3. Silicone oil poly(dimethylsiloxane) from Dow Corning Corporation, with density ρ=950 kgm-3 viscosity η=0.2·10−4 m2-1s and surface tension o=20 mNm−1 at 25° C. was used as a top liquid (3 mm deep). The reported interfacial tension between pure water and silicone oil is of the order of o12=40 mNm−1, the inter facial tension can be as low as 10 mNm because of the presence of surfactants, salt, and interface contamination. The colloidal suspension was energized by a uniform vertical alternating magnetic field, Hac=H0 sin(2π ft), applied perpendicular to the interface. The amplitude of the ac magnetic field H0 was in the range of 50-250 Oe and the frequency f was in the range of 10-120 Hz. A static in-plane magnetic field up to 40 Oe was created by two pairs of orthogonal precision Helmholtz coils. The experimental set-up was built as originally described in Snezhko A., Aranson I. S, & Kwok W.-K. Surface wave assisted self-assembly of multidomain magnetic structures. Phys. Rev. Lett. 96, 078701 (2006), which is incorporated by reference herein. Particle image velocimetry (PIV) was performed in the bottom liquid layer using a laser sheet illumination technique 30. Tracer particles (Kalliroscope tracers, PM-01, Kalliroscope) were introduced into the bulk of the bottom layer. Vertical and horizontal slices of the flow pattern were acquired. Horizontal slices were taken at a depth of 0.5 mm below the interface. 1 mm (Ceroglass GSR-11) and 0.4 mm (Ceroglass SLYTZ-5) glass beads were used as cargo particles to demonstrate simple robotic functionality of asters and membranes.
The force exerted by an aster on a 1 mm spherical bead can be estimated from the drag force acting on a moving sphere in a viscous media. For a d=1 mm bead moving with a speed V of approximately 1 cm s−1 in a water/silicone oil mixture (ratio of viscosities 1:20, so the main contribution to the friction comes from the more viscous oil layer, the viscous drag force is then F=3πdVη≈10−6 N. Correspondingly, the torque can be estimated from the maximal rate of rotation of the aster in response to a rotation of the in-plane magnetic field, which is in most of the cases about w=1-2 Hz. The viscous torque is then given by T=πd3wη≈10−9 Nm.
Evaluation of structure's drift velocity as a function of the in-plane magnetic field is a formidable problem: it is intrinsically nonlinear due to the nature of large-scale (rectified) flow generated by an aster. In one aspect of the invention, a simplified yet non-trivial model captures salient features of the observed phenomenon: the onset of motion in a response to the in-plane magnetic field and cessation of motion with further increase of the field.
Instead of the three-dimensional Navier-Stokes equation for an aster the one-dimensional Burgers equation with two point-point pressure sources—stresslets (since no net external force is applied to the aster, the point sources should be force dipoles) is considered. Despite its nonlinearity, the equation is fully integrable by the means of the Hopf-Cole transformation. The equations is of the form:
Here u denotes the hydrodynamic velocity. Note that incompressibility condition is not enforced: the non-zero 1D flow divergence δxu≠0 can be interpreted as a flow generation in the orthogonal direction. Viscosity η and the distance between sources L is scaled to 1. In this simplified description only a slowly-varying (i.e. averaged over the period 2π/f of the applied vertical magnetic field) large-scale flow generated by an aster is considered. The time-periodic component of the flow decays exponentially away from the source and does not contribute directly to the drift velocity.
The nonlinear equation was selected to describe the self-interaction of aster's rectified flows. Aster is replaced by an asymmetric rigid dumbbell: two point pressure sources with amplitudes m1,m2>0 located at the distance L and drifting as a whole with a velocity V, see
This assumption that aster's asymmetry m1−m2 is proportional to the in-plane magnetic field H was validated, see
Thus, for this embodiment, the model describes a cross-section through the center of an aster in the direction of the in-plane field H. In isolation (e.g. m2=0, it corresponds to a completely opened aster or a plane segment with the magnetic chains parallel to the in-plane field H), each source does not drift and creates an anti-symmetric flow: u=−m1/2 for x<0 and u=m1/2 for x>0. The drift emerges as a result of a nonlinear interaction between the flows generated by each source.
The drift velocity V is determined from the force balance condition exerted by the flow on each point source. The sources are assumed to be rigidly connected and maintaining the distance L in the course of motion. To determine the drift velocity V, the total force F exerted by the flow on two particles is stated as zero (no external force is applied to the aster). Thus the total force F is of the form (includes contributions acting on each particle and proportional to relative velocity u-V):
F=κ(m1(u1−V)+m2(u2−V))=0 (3)
Here u1,2 are the mean flow velocities at the location of each particle, κ is the mobility constant. Because the flow is discontinuous at the δ-functions, u1,2=(u1,2++u1,2−)/2 where u± denotes the values of flow right/left of the δ-function. Here it was set that viscous drag on each particle is proportional to its size (compare to the Stokes law) determined in turn by the corresponding magnetic moment m1,2. Therefore, excluding V from Eq. (2), expression for the drift velocity is obtained:
If the drift velocity V is small compared to u, ηtu in Eq. (1) may be neglected. This technical assumption allows significant simplification of the calculations. Replacing x→x−Vt, and dropping ∂tu term, integrating Eq. (2) yields
∂xu−u2+m1δ(x)+m2δ(x−1)=−u−2=const (5)
where ū>0 is an integration constant to be determined. The solution for x<0 is u=−ū and u=ū for x>1. For 0<x<1 the solution is obtained by integration of Eq. (5):
u=−ū tan h(ū(x−xo)) (6)
where x0 is another constant to be determined. This solution has to be matched at the points x=0, 1 to the solution outside the interval using jump conditions u1,2+−u1,2−=m1,2 at the δ-functions. From integration over the δ-functions the following is obtained:
−ū tan h(ū(−x0))+ū=m1 (7)
ū tan h(ū(1−x0))+ū=m2 (7)
Eqs. (7) uniquely define the constants ū, x0 as functions of m1,2, and, in turn, yield an explicit expression for the drift velocity V. Note that if m2=0 correct flow is receovered for a single source: u=−m1/2 for x<0 and u=m1/2 for x>0. Explicit form for V (using Eq. (4) and Eq. (8)) is
Solving numerically transcendental Eqs. (7) and plugging x0, ū into Eq. (8) obtains dependence of the drift velocity V vs m1,2 shown in
To fit experimental data, m1−m2=H and m1+m2=Hc=const. The resulting fitting curve is in a good agreement with the experimental data show in
V˜m1m2(m1−m2)˜H(Hc2−H2) (9)
The foregoing description of illustrative embodiments has been presented for purposes of illustration and of description. It is not intended to be exhaustive or limiting with respect to the precise form disclosed, and modifications and variations are possible in light of the above teachings or may be acquired from practice of the disclosed embodiments. It is intended that the scope of the invention be defined by the claims appended hereto and their equivalents.
The United States Government claims certain rights in this invention pursuant to Contract No. DE-AC02-06CH11357 between the United States Department of Energy and UChicago Argonne, LLC, representing Argonne National Laboratory.
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Number | Date | Country | |
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20130075648 A1 | Mar 2013 | US |