Separation using angled acoustic waves

Information

  • Patent Grant
  • 11021699
  • Patent Number
    11,021,699
  • Date Filed
    Friday, March 30, 2018
    6 years ago
  • Date Issued
    Tuesday, June 1, 2021
    3 years ago
Abstract
Methods and systems for separating material from a host fluid use an acoustophoresis device. These methods and systems can deflect material (e.g., a second fluid, cells, beads or other particles, exosomes, viruses, oil droplets) in host fluid streams at high flow rates.
Description
BACKGROUND

In the medical field, it often is desirable to separate low concentration cells from a fluid mixture with no harm to the cells, wash cells, concentrate cells in a fluid mixture, differentiate cells based on key parameters, or even fractionate many different types of cells. Such processes are key in the development of possible cures to many common diseases. It may also be desirable to separate particles or cells different in size, density and or acoustic contrast factor using an acoustic field where the particles may be separated from each other as well. Examples include the separation of live from dead cells and the separation of differentiated from undifferentiated cells. The methods described herein provide for such a separation or fractionation method that is label-free.


In the food and beverage industry, filter cartridges and filter membranes have conventionally been used to filter particles from liquids. Such filters are expensive and become clogged and non-functional as material is processed. In contrast, acoustophoresis provides, among other possible advantages, a solid-state, low-cost alternative to filter cartridges and filter membranes that is capable of processing large quantities of a host medium, for example water or beer, that is laden with yeast or other suspended particles.


In the food and beverage industry, host fluid is flowed through filters at flow rates up to ten times greater than those through conventional acoustophoresis devices. At these higher flow rates, trapping of the particles in the host fluid is decreased, thereby leading to decreased separation efficiency. It would therefore be desirable to provide systems and methods capable of separating a second fluid or a particulate from a host fluid at much higher flowrates, or at much lower concentrations, than conventional macro-scale acoustic separators.


In the oil and water industry, efficiently and economically separating oil and other contaminants from water has become an important process. The rise of fracking techniques has led to many settling ponds and large costs for transportation of contaminated water. These settling ponds are a challenge to the environment and better means are needed to clarify fracking water more effectively. Acoustophoresis provides, among other possible advantages, a solid-state, effective means of clarifying fracking, but the flow rates associated with such macro-scale acoustophoresis devices is still too low to be feasible. It would therefore be desirable to provide systems and methods capable of separating a second fluid, cell, or particulate from a host fluid at much higher flowrates.


SUMMARY

This disclosure describes various embodiments of mini to macro-scale systems, devices, and methods for acoustophoresis to separate, fractionate, isolate, concentrate, wash, detect, or even differentiate cells or particles in fluid suspension. The devices and methods include a flow chamber and an ultrasonic transducer and reflector that set up an angled acoustic standing wave oriented at an acute angle relative to the direction of mean flow through the flow chamber, which includes the particle path through the angled acoustic standing wave. At higher flow rates, acoustic standing waves may be used to deflect the particles in a desired direction, without causing the particles to become trapped in the standing wave. By applying the acoustic standing wave to the host fluid at an angle thereto, desired deflection of the particles can be achieved.


These systems and methods can separate, sort, and differentiate various particles using bulk ultrasonic standing waves oriented at an angle γ relative to the fluid velocity. This approach offers a sensitive separation capability with respect to size and acoustic contrast of particles.


In one aspect, systems for separating material from a host fluid include: a flow chamber defining a direction of mean flow; an ultrasonic transducer including a piezoelectric material configured to be excited to generate an angled bulk acoustic standing wave with a wavelength and an acoustic radiation force in the flow chamber oriented at an acute angle relative to the direction of mean flow through the flow chamber, wherein the flow chamber has a minimum internal dimension that is at least 10 times the wavelength of the angled acoustic standing wave; a reflector opposite the at least one ultrasonic transducer; a first inlet fluidly connected to the flow chamber; a second inlet fluidly connected to the flow chamber; a first outlet fluidly connected to the flow chamber; and a second outlet fluidly connected to the flow chamber. Embodiments of these systems can include one or more of the following features.


In some embodiments, the first inlet is at least 0.1 inches (e.g., 0.2, 0.3, 0.4, 0.5, or 1 inch) from the angled bulk acoustic standing wave.


In some embodiments, systems also include a first channel ending at the first inlet, wherein the first channel has a substantially straight section extending at least 0.1 inches (e.g., 0.25, 0.5, 0.75, or 1 inch) from the first inlet.


In some embodiments, a space between the ultrasonic transducer and the reflector comprises a first portion within the flow chamber and a second portion outside the flow chamber. In some cases, systems also include an acoustically transparent material separating the first portion from the second portion. In some cases, systems also include a cooling water system in fluid connection with the second portion. In some cases, the second portion is filled with solid material having an acoustic impedance equal to an acoustic impedance of the host fluid.


In some embodiments, the system comprises a plurality of ultrasonic transducers.


In some embodiments, the first inlet and the second inlet are coaxial. In some cases, the first outlet and the second outlet are coaxial. In some cases, the first inlet has a rectangular cross-section. In some cases, an area of the rectangular cross-section of the first inlet is at least 0.05 square inches (e.g., 0.1, 0.25, 0.5, 0.75, or 1 inch).


In some embodiments, the first inlet has an aspect ratio of at least 5 (e.g., 10, 15, 20, 25, or 50).


In some embodiments, systems also include a third outlet, wherein second outlet is disposed between the first outlet and the third outlet and a cross-sectional area of the third outlet is smaller than a cross-sectional area of the second outlet. In some cases, the second outlet has a rectangular cross-section and third outlet has a rectangular cross-section. In some cases, a width of the second outlet is the same as a width of the third outlet. In some cases, a height of the second outlet is at least 2 times a height of the third outlet.


In some embodiments, systems also include a plurality of third outlets, each of the plurality of third outlets offset from an axis of the second outlet in a direction of deflection of the angled acoustic wave.


In some embodiments, systems also include a first channel ending at the first inlet, wherein the first channel has a substantially straight section extending at least 0.1 inches (e.g., 0.25, 0.5, 0.75, or 1 inch) from the first inlet at a first acute angle relative to a plane perpendicular to the angled acoustic standing wave. In some cases, a second channel ending at the second inlet, wherein the second channel has a substantially straight section extending at least 0.1 inches (e.g., 0.25, 0.5, 0.75, or 1 inch) from the second inlet at a second acute angle relative to the plane perpendicular to the angled acoustic standing wave. In some cases, the first acute and the second acute angle are equal. In some cases, system also include a third channel ending at the first outlet, wherein the third channel has a substantially straight section extending from the first outlet at a third acute angle relative to the plane perpendicular to the angled acoustic standing wave. In some cases, the first acute and the third acute angle are equal. In some cases, systems also include a fourth channel ending at the second outlet, wherein the first outlet located in a direction of deflection of the angled acoustic wave relative to the second outlet, wherein the fourth channel has a first cross-sectional area, the third channel has a first section with the first cross-sectional area and a second section with a second cross-sectional area that is smaller than the first cross-sectional area, and the second section of the third channel is located between the first outlet and the first section of the third channel. In some cases, the third channel has a substantially straight section extending from the first outlet at a third acute angle. In some cases, the first acute angle is between 80 degrees and 90 degrees.


In some embodiments, a wall of the flow chamber adjacent to the first outlet in a direction of deflection of the angled acoustic wave extends at an acute angle relative to a plane perpendicular to the angled acoustic standing wave. In some cases, the acute angle is between 1 and 20 degrees (e.g., more than 2 degrees, more than 3 degrees, more than 5 degrees, more than 10 degrees, less than 15 degrees, less than 10 degrees, less than 7.5 degrees, less than 5 degrees).


In one aspect, systems for separating material from a host fluid include: a flow chamber extending between a first end and a second end; an inlet located at the first end of the flow chamber; a first outlet located at between the first end of the flow chamber and the second end of the flow chamber, the inlet and the first outlet defining a direction of mean flow through the flow chamber; an ultrasonic transducer including a piezoelectric material configured to be excited to generate an angled acoustic standing wave between the inlet and the first outlet, the angled acoustic standing wave with a wavelength and an acoustic radiation force in the flow chamber oriented at an acute angle relative to the direction of mean flow through the flow chamber; and a reflector opposite the at least one ultrasonic transducer; wherein the first outlet is spaced apart from the second end of the flow chamber.


In some embodiments, the flow chamber has a minimum internal dimension that is at least 10 times the wavelength of the angled acoustic standing wave.


In some embodiments, the first outlet is located at least 0.5 inches from the second end of the flow chamber.


In some embodiments, the flow chamber has a distance between the first end and the second end and the first outlet is located at away from the second end by at least 30% of the distance. In some cases, the first outlet is located at away from the second end by at most 70% of the distance.


In some embodiments, systems also include a second outlet located at the second end of the chamber.


In one aspect, methods of separating material from a host fluid include: flowing an initial mixture of the host fluid and the material via an inlet into an acoustophoretic device at a flow rate, the acoustophoretic device including: an acoustic chamber communicating with the inlet; an ultrasonic transducer coupled to the chamber and arranged to be excited to produce an acoustic wave at an angle with a mean direction of flow of the initial mixture; controlling a ratio of acoustic radiation force produced by the ultrasonic transducer and a viscous drag force of the initial mixture to cause a first subgroup of the material passing through the acoustic wave to deflect at an angle that is different than that of a second subgroup of the material, to thereby permit the first and second subgroups to be separated. Embodiments of these methods can include one or more of the following features.


In some embodiments, methods also include controlling the ratio by controlling one or more of the angle, the flow rate, a frequency of excitation of the ultrasonic transducer or power supplied to the ultrasonic transducer.


In some embodiments, methods also include controlling the ratio based on characteristics of one or more subgroups. In some cases, methods also include controlling the ratio based on one or more of material size, density, compressibility or acoustic contrast factor.


In some embodiments, methods also include controlling the ratio to deflect at least some of the material at the angle of the acoustic wave.


In some embodiments, the material further includes a third subgroup that is different from the first subgroup and the second subgroup, and controlling the ratio further comprises causing the third subgroup to deflect at an angle that is different than that of the first subgroup or the second subgroup.


In some embodiments, methods also include controlling the ratio in a range that is determined by characteristics of subgroups of materials in the mixture to be separated. In some cases, the range is determined by the relative sizes of the material in the subgroups to be separated. In some cases, the range spans at least an order of magnitude.


In some embodiments, methods also include collecting the first subgroup or the second subgroup in a collection duct communicating with the acoustic chamber.


In some embodiments, the material comprises particulates, cells, or fluids, that include at least two subgroups possessing different characteristics.


These systems and methods can separate, sort, and differentiate various particles using bulk ultrasonic standing waves oriented at an angle γ relative to the fluid velocity. This approach offers a sensitive separation capability with respect to size and acoustic contrast of particles.


“Bulk acoustic standing waves” indicate acoustic waves that propagate through volume of a medium such as water with little attenuation. In contrast, “surface acoustic standing waves” are acoustic waves that travel along the surface of a material exhibiting elasticity, with an amplitude that typically decays exponentially with depth into the substrate. Surface acoustic waves do not penetrate very far into a volume of a medium such as water, e.g. several millimeters from a substrate into the water volume at most.


The singular forms “a,” “an,” and “the” include plural referents unless the context clearly dictates otherwise.


Numerical values should be understood to include numerical values which are the same when reduced to the same number of significant figures and numerical values which differ from the stated value by less than the experimental error of conventional measurement technique of the type described in the present application to determine the value.


All ranges disclosed herein are inclusive of the recited endpoint and independently combinable (for example, the range of “from 2 grams to 10 grams” is inclusive of the endpoints, 2 grams and 10 grams, and all the intermediate values). The endpoints of the ranges and any values disclosed herein are not limited to the precise range or value; they are sufficiently imprecise to include values approximating these ranges and/or values.


The modifier “about” used in connection with a quantity is inclusive of the stated value and has the meaning dictated by the context. When used in the context of a range, the modifier “about” should also be considered as disclosing the range defined by the absolute values of the two endpoints. For example, the range of “from about 2 to about 10” also discloses the range “from 2 to 10.” The term “about” may refer to plus or minus 10% of the indicated number. For example, “about 10%” may indicate a range of 9% to 11%, and “about 1” may mean from 0.9-1.1.


It should be noted that some of the terms used herein may be relative terms. For example, the terms “upper” and “lower” are relative to each other in location, i.e. an upper component is located at a higher elevation than a lower component in a given orientation, but these terms can change if the device is flipped. The terms “inlet” and “outlet” are relative to a fluid flowing through them with respect to a given structure, e.g. a fluid flows through the inlet into the structure and flows through the outlet out of the structure. The terms “upstream” and “downstream” are relative to the direction in which a fluid flows through various components, i.e. the flow fluids through an upstream component prior to flowing through the downstream component. It should be noted that in a loop, a first component can be described as being both upstream of and downstream of a second component.


The terms “horizontal” and “vertical” are used to indicate direction relative to an absolute reference, i.e. ground level. However, these terms should not be construed to require structures to be absolutely parallel or absolutely perpendicular to each other. For example, a first vertical structure and a second vertical structure are not necessarily parallel to each other. The terms “top” and “bottom” or “base” are used to refer to surfaces where the top is always higher than the bottom/base relative to an absolute reference, i.e. the surface of the earth. The terms “upwards” and “downwards” are also relative to an absolute reference; upwards is always against the gravity of the earth. It is to be understood that gravity, or the effects of gravity, are negligible in the angled wave deflection process described herein, because the process works on individual particles, not much larger particle clusters as used in other systems.


The term “parallel” should be construed in its lay sense of two surfaces that maintain a generally constant distance between them, and not in the strict mathematical sense that such surfaces will never intersect when extended to infinity.


Two numbers are of the same order of magnitude if the quotient of the larger number divided by the smaller number is a value of at least 1 and less than 10.


The details of one or more embodiments of these systems, devices, and methods are set forth in the accompanying drawings and the description below. Other features, objects, and advantages will be apparent from the description and drawings, and from the claims.





DESCRIPTION OF DRAWINGS


FIG. 1 is a schematic of particle deflection by the acoustic radiation force of an angled acoustic standing wave oriented at an angle γ relative to the flow velocity V.



FIGS. 2A and 2B are schematics of the normal and tangential velocity components for a left running acoustic standing wave (FIG. 2A), and a right running acoustic standing wave (FIG. 2B).



FIG. 3 is a schematic of the Galilean transformation decomposing the angled acoustic standing wave system into a system of two equations, i.e., normal to the wavefront and tangential to the wavefront.



FIG. 4 is a schematic illustration of net particle deflection by the tangential velocity component after a one-half wavelength propagation in the normal direction to the wavefront.



FIG. 5 is a plot of particle deflection angle ΔθM versus wave angle γ for M parameter values of 0 to 1.



FIG. 6 is a plot of particle deflection angle ΔθM versus M parameter for acoustic standing wave angles of 30°, 45°, and 60°.



FIG. 7A is a plot of particle deflection angle ΔθM versus M parameter curve highlighting two possible regions of particle deflection. FIG. 7B is a schematic of a particle deflection angle ΔθM at an angle less than the wave angle γ and FIG. 7C is a schematic of a particle deflection angle ΔθM that equals the wave angle γ.



FIGS. 8A and 8B show the numerical particle deflection trajectory for a CHO cell for (a) M/sin λ value less than one and (b) M/sin λ value greater than one for a frequency of 2 MHz, an acoustic pressure amplitude of 1 MPa, a particle diameter of 18 μm, and an acoustic contrast factor of 0.03.



FIG. 9A shows the numerical particle deflection trajectory for CHO cells of diameter 16, 18, and 20 μm and acoustic contrast factor of 0.03. FIG. 9B shows the numerical particle deflection trajectory for CHO cells of diameter 20 μm and acoustic contrast factors of 0.03, 0.035, 0.04, 0.045, and 0.05. Frequency is 2 MHz, acoustic pressure amplitude is 1 MPa and velocity amplitude is 6 cm/min.



FIG. 10 shows numerical particle trajectories for a CHO cell as a function of velocity magnitude of the fluid through the channel.



FIG. 11A is a chart comparing the universal analytical predictions for particle deflection with numerical particle trajectories over a wide range of M values.



FIGS. 11B and 11C are charts comparing the universal analytical predictions for particle deflection, with numerical particle trajectories over a wide range of M values



FIG. 12A-12G show an angled wave device (AWD) system with a 45° angled standing wave. FIG. 12A is a photograph of the AWD system with multiple flow inlets on the right and multiple flow outlets on the left. FIG. 12B is a schematic of the setup showing locations of the transducer, reflector and flow channels. FIG. 12C is a schematic illustrating one possible mode of operation of the AWD with the dash lines representing the nodal plane locations of the standing wave. FIG. 12D is a schematic of the flow profiles within the AWD. FIG. 12E is a cross-section of the AWD and FIGS. 12F and 12G are cross-sections of alternate duct arrangements for the AWD.



FIG. 13 is a particle size distribution of the polystyrene beads used in experiments.



FIGS. 14A-14F are photos of polystyrene bead deflection as a function of electrical power to the 1 MHz transducer setting up an acoustic standing wave at a 45°.



FIGS. 15A and 15B illustrate an AWD system configured for concentrating particles or cells by lowering the mixture duct and constricting the lower buffer stream.



FIG. 16 is a schematic of an AWD system configured for particle fractionation.



FIGS. 17A, 17B, and 17C are schematics illustrating aspects of an angled fluid device (AFD) system. FIG. 17A shows system geometry and flow characteristics.



FIG. 17B shows particle transfer between fluids. FIG. 17C schematically depicts the fluid flow direction of the system.



FIG. 18A is a photograph of the AFD and FIG. 18B is a schematic of the setup showing fluid streamlines from a CFD prediction.



FIGS. 19A and 19B are photographs of the acoustic chamber window of the AFD system showing particle movement through the AFD system without acoustics (FIG. 19A) and with acoustics (FIG. 19B).



FIGS. 20A and 20B are, respectively, a cross-section and a schematic of a system in which a flow construction is used to increase the concentration of the particle mixture separated using the system.



FIG. 21 is a schematic of an AFD system designed for particle fractionation.



FIGS. 22A, 22B, and 22C are, respectively, a schematic, a plot of modeled flow velocities, and a cross-section of an AFD system designed for particle collection.



FIGS. 23A and 23B are, respectively, a cross-section and a schematic of a low angle AFD system.



FIGS. 24A-24 C present the results of using an AWD system to fractionate T-cells from 35 um beads. FIGS. 24A and 24 B are schematics illustrating the anticipated separation of T-cells from beads. FIG. 24C is a chart of the results.



FIGS. 25A-25C present the results of using an AWD system to fractionate a mixed population of beads. FIG. 25A is a schematic illustrating the anticipated separation of larger beads from smaller beads. FIGS. 25B and 25C are charts of the results.



FIGS. 26A-26C present the results of using an AWD system to fractionate a population of PMMA beads. FIGS. 26A, 26B, and 26C show the distribution of beads between the center outlet and the buffer outlet without acoustics, with 1 W of power applied and with 1.2 W of power applied.



FIG. 27 shows a 10-degree AWD system with a center channel and a buffer channel around it.



FIG. 28 shows an AWD system that has one small inlet on a side, buffer flow on top of it, and 5 outlets where different fractions from a mixture population will end up.



FIG. 29 shows an AWD system in which viewing of the flow is made possible by 2 glass windows.





Like reference symbols in the various drawings indicate like elements.


DETAILED DESCRIPTION

The present disclosure relates to acoustophoretic devices that employ multi-dimensional ultrasonic acoustic standing waves, planar acoustic standing waves or combinations of planar and multidimensional acoustic standing waves (collectively referred to herein as angled acoustic standing waves) oriented at an angle relative to the direction of mean flow through the device. The direction of mean flow through the chamber is to be understood to include the path traveled by a second fluid, cell, or particulate that is flowed through an angled acoustic standing wave generated in the device. These angled acoustic standing waves deflect particles in a host fluid stream, rather than trapping the particles for agglomeration. This is an important distinction from many current acoustophoresis devices. These devices described can operate at high flowrates and can be used to replace costly and clog-prone filter cartridges and filter membranes in various industries. The devices and methods of the present disclosure rely primarily on the axial force component to deflect the particles out of the acoustic field, rather than relying on trapping, agglomeration, and gravitational and buoyancy forces. The devices and methods presented herein are capable of being operated independent of gravity (i.e., in any orientation), and do not rely on gravitational settling. In this way, the axial force of an angled acoustic standing wave oriented at an angle relative to the flow direction is capable of advantageously deflecting material (e.g., a second fluid, cells, beads or other particles, exosomes, viruses, oil droplets) in host fluid streams at high flow rates of up to about 400 mL/min, and more preferably up to about 600 mL/min or about 700 mL/min in devices with a cross section of 1 inch by 1 inch. Devices have also been produced with a 0.5 inch×0.5 inch total flow channel, with the center inlet being 0.1 inch×0.1 inch. For these devices, volumetric flow rates on the order of 0 to 100 ml/min with typical buffer flow rate of 20 to 100 ml/min and center flow rate of 1 to 10 ml/min. This corresponds to linear velocities on the order of 1 to 100 mm/sec regardless of the size of the device.


Thus, bulk acoustic standing waves angled relative to a direction of flow through a device can be used to deflect, collect, differentiate, or fractionate particles or cells from a fluid flowing through the device. The angled acoustic standing waves can be used to separate or fractionate particles in the fluid by size, density, speed of sound, or shape. The angled acoustic standing wave can be a three-dimensional acoustic standing wave. The acoustic standing wave may also be a planar wave where the piezoelectric material is excited in a piston fashion or the acoustic standing waves may be a combination of the planar acoustic standing waves and the multidimensional acoustic standing waves. For the purposes of this disclosure, a standing wave where the lateral force is at least an order of magnitude less than the magnitude of the axial force is considered a “planar acoustic standing wave.” However, standing waves that are not planar acoustic standing waves may be used with the approaches described in this disclosure as well. This can be used to separate live cells from dead cells, damaged cells from healthy cells, or differentiated from undifferentiated cells. The deflection of the particles by the standing wave can also be controlled or amplified by the strength of the acoustic field, the angle of the acoustic field, the properties of the fluid, the three dimensionality of the standing wave, the frequency of the standing wave, the acoustic chamber shape, and the mixture flow velocity.


When acoustic standing waves propagate in liquids, the fast oscillations may generate a non-oscillating force on particles suspended in the liquid or on an interface between liquids. This force is known as the acoustic radiation force. The force originates from the non-linearity of the propagating wave. As a result of the non-linearity, the wave is distorted as it propagates and the time-averages are nonzero. By serial expansion (according to perturbation theory), the first non-zero term will be the second-order term, which accounts for the acoustic radiation force. The acoustic radiation force on a particle, or a cell, in a fluid suspension is a function of the difference in radiation pressure on either side of the particle or cell. The physical description of the radiation force is a superposition of the incident wave and a scattered wave, in addition to the effect of the non-rigid particle oscillating with a different speed compared to the surrounding medium thereby radiating a wave. The following equation presents an analytical expression for the acoustic radiation force FR on a particle, or cell, in a fluid suspension in a standing wave.










F
R

=



3

π






P
0
2



V
P



β
f



2

λ



X






sin


(

2

kx

)







(
1
)








where βm is the speed of sound in the fluid medium, ρ is density, X is acoustic contrast factor, VP is particle volume, λ is wavelength, k is 2π/λ, P0 is acoustic pressure amplitude, x is the axial distance along the standing wave (i.e., perpendicular to the wave front), and









X
=


1
3

[




5


ρ
ρ


-

2


ρ
f





2


ρ
ρ


+

ρ
f



-


β
ρ


β
f



]





(
2
)








where ρρ is the particle density, ρf is the fluid medium density, βρ is the compressibility of the particle, and βf is the compressibility of the fluid medium.


The acoustic radiation force on a particle is seen to be a symmetric function having a period that is one half the acoustic wavelength. This means the radiation force distribution repeats every half wavelength. This also means a particle will be accelerated and decelerated by the radiation force presented by Eq. (1).



FIG. 1 schematically shows the particle deflection that such a force variation will generate when a mixture flows through a standing wave at an angle, γ. V is the velocity of the mixture of fluid and particles. The pluses and minuses in the figure represent the direction of the radiation force. Plus sign means the radiation force is in the flow direction and increases particle velocity, and minus sign means the radiation force slows down the particle. The particles will always be deflected toward the wave front, or away from the wave axial direction as shown. FIG. 1 is a left running wave, or the wave slants to the left when looking in the direction of the fluid mixture flow.



FIGS. 2A and 2B are schematics of the normal and tangential velocity components for a left running acoustic standing wave (FIG. 2A), and a right running acoustic standing wave (FIG. 2B). As shown in FIGS. 2A and 2B, the fluid velocity (V) in FIG. 1 can be decomposed into a velocity component perpendicular to the running wave (VN), and one parallel to the wave (VT). The particles will always be deflected in the direction of the tangential velocity component. It is the fluid motion in the tangential direction that carries, or drags the particle at a constant velocity, as the normal velocity component is slowed down or sped up by the axial radiation force. In this case, any particle in suspension will again be deflected in the VT direction.


An angled flow problem, as presented in FIG. 2 can often be analyzed more simply by using a Galilean transformation, as shown in FIG. 3. This transformation amounts to looking at the same problem while running along the wave at a velocity VT. Theoretically, the physics of the problem do not change with such a transformation. As seen in FIG. 3, this amounts to solving the flow through a standing wave with the flow direction perpendicular to the wave front, or in the axial direction of the wave. In this direction, the acoustic radiation force variation, as presented in Eq. (1), will result in a symmetrical series of velocity increases and decreases in the normal flow direction. Using ν as the particle perturbation velocity resulting from the acoustic radiation forces on a particle as the mixture flows through a normal acoustic standing wave, the following governing equation can be generated to describe the particle trajectory (i.e. from Newton's second law, Eq. (1) and Stokes' drag), where rp is particle radius:












ρ
ρ




V
P



(

dv
dt

)



+

6

πμ






r
p


v


=



3

π






P
0
2



V
P



β
f



2

λ




X


(

β
,
ρ

)








sin


(

2

kx

)







(
3
)








As such, ν is actually ΔVN, or the change in particle velocity normal to the standing wave resulting from the effects of the acoustic radiation forces on the particles as generated by the standing wave relative to the normal fluid flow velocity. The viscosity effects always oppose the perturbation velocity, and act in a direction toward the mean velocity. As a result, the viscosity always drives the particle perturbation velocity to fluctuate about the mean flow velocity with an amplitude of ΔVN. The particles in suspension are assumed small enough to instantly react to the viscous and radiation forces. With this assumption, the first term on the left side drops out, and Equation 3 can be reduced to:

v=C sin(2kx)  (4)

where







C
=


π
3





r
p
2



β
m


φ

μλ



P
0
2



,





C is the maximum perturbation velocity in the normal direction and is seen to be a function of the acoustic pressure amplitude, particle radius, acoustic contrast factor, fluid viscosity and the acoustic wavelength. With this assumption, the particle velocity instantly adjusts to the Stokes velocity generated by the radiation force.



FIG. 4 schematically presents the particle deflection effect caused by the decrease and increase of the velocity component normal to the acoustic standing wave, when the standing wave is at an angle γ to the flow. As inferred by the Galilean transformation, the tangential velocity component has to remain constant as the velocity component normal to the acoustic standing wave varies symmetrically about the mean normal velocity.


The trajectory of the fluid compared to the average trajectory of a particle are also shown in FIG. 4. P1P2 is the fluid trajectory during a time period Δt0. P1P3 is the average particle trajectory. VN is the component of velocity perpendicular to the wave, VT is the tangential component of the velocity along the wave front, V is the incoming mixture velocity, t is time, and ΔθM is particle deflection from the fluid direction. P1 is where the mixture enters the half wavelength of a standing wave. A planar standing wave is assumed. The fluid is not deflected by the radiation forces and leaves the half wavelength at P2 which is horizontally aligned with P1, in the direction of fluid velocity. On the other hand, the particle is carried down the wave front by the tangential component of the fluid velocity, and is deflected to P3 as seen in the figure. The phrase “a direction of deflection of the angled acoustic wave” is used to indicate the direction of this deflection.


The problem of interest is to determine the particle deflection with acoustic wave angle under different flow and acoustic conditions. ΔVN is the maximum normal velocity perturbation, C, associated with a sinusoidal acoustic radiation force acting on a particle as shown in Eq. (4).


Particle or cell deflection can be characterized ΔV_N/V which is a non-dimensional parameter that will be defined as M in the following analytical equation development:









M
=


Δ






V
N


V





(
5
)








which can be expanded to









M
=


C
V

=


π
3





r
p
2



β
f



P
0
2


X


μλ





V








(
6
)








where C is the maximum normal velocity perturbation (ΔVN) from Eq. (4), and V is the fluid free stream velocity. This non-dimensional parameter, M, is important since it represents the ratio of acoustic radiation force on a particle, to the viscous drag force on the particle. M is the key parameter for particle deflection by an angled standing wave. Both acoustic pressure and particle size are squared in the expression. This means they are the most dominant factors for determining particle deflection. An accurate expression for particle deflection in an angled wave, in terms of M, can be obtained by solving particle movement with the normal wave, and then transforming the results to the angled wave flow field (i.e., using the Galilean transformation presented in FIG. 3). The Galilean transformation has no effect on time. Therefore, the time of transit between half wavelengths (which repeat) will be the same in the normal wave plane, and the transformed angled wave plane.


Equation 7 presents an expression for ΔtM which is the time it takes a particle in suspension to travel through one half wavelength of the normal standing wave (i.e. process repeats every half wavelength) as it is being accelerated and decelerated by the acoustic axial radiation force. Equation 8 is the expression for Δto which is the time it takes the fluid to pass through one half wavelength of the normal wave. These two time values are independent of the Galilean transformation, and combined with FIG. 4, can be used to obtain particle deflection from the fluid flow direction










Δ






t
M


=




0





λ




/

2





dx


V
N

+

Δ






V
N






sin





2

kx




=


1

V
N






0





λ




/

2





dx

1
+


M

sin





λ



sin





2

kx










(
7
)







Δ






t
o


=


λ


/


2


V
N






(
8
)








The ratio of these times is defined as









ɛ
=


Δ






t
M



Δ






t
o







(
9
)








Equations 10 and 11 use ε combined with the wave angle γ to generate an expression for particle deflection in the angled wave field.










tan






θ
M


=



Δ






t
M



V
T



Δ






t
o



V
N



=

ɛ

tan





γ







(
10
)







Δ






θ
M


=



tan

-
1




(

ɛ

tan





γ


)


-

π
2

+
γ





(
11
)








FIG. 4 helps interpret Eq. (10) and (11). The angled waves in FIG. 4 represent the results of transforming the normal wave by adding VT to all the velocities. P1 is the point that the flow mixture enters the standing wave. The standing wave is at an angle γ with respect to the flow direction. The dash wave lines represent regions in the standing wave where the radiation forces on the particles are zero. The direction of the radiation forces reverse when crossing the dash lines shown in FIG. 4. P2 and P3 are points on the zero force line that is λ/2 distance away from P1. The particle in suspension when flowing through P1 will be deflected by the acoustic wave and will pass through P3 as shown in FIG. 4. P2 is the point it would have passed through with no acoustic radiation forces, and it represents the fluid flow direction. The dashed line connecting P1 and P3 represents the average trajectory of the particle through one cycle of the acoustic radiation force. θM is the total angle that the same line makes with the normal direction of the wave. Therefore, ΔθM is the particle deflection angle generated by the acoustic wave as measured from the flow direction (i.e. dash line connecting P1 and P2). The particle transit times calculated from the normal wave analysis are used with the tangential velocity transformation to get particle displacements in the wave front direction. The particle wave front distance generated by the transformation with no radiation forces is ΔtoVT and the particle wave front distance generated by both the Galilean transformation and the integrated effects of acoustic radiation forces on the movement is ΔtMVT. The difference (ΔtoVT−ΔtMVT) is the particle deflection along the wave front direction generated by the sinusoidal acoustic radiation forces acting on the particle. For ΔθM, or particle deflection angles, to be calculated at different wave angles and different deflection parameters, M, the integral expression for epsilon has to be solved in Eq. (11).


An analytical solution for particle deflection as a function of wave angle and the non-dimensional parameter, M, defined by the ratio of acoustic radiation forces and viscous forces on a mixture flowing through an acoustic standing wave, was developed using substitution of variables. This analytical solution which allows particle deflection angle to be predicted for all values of M and γ, is shown in Eq. (12).










Δθ
M

=

{






tan

-
1




(

1

tan





γ



1
-


(

M

sin





γ


)

2





)


-

π
2

+
γ





if


M

sin





γ



<
1





γ




if


M

sin





γ




1









(
12
)








FIG. 5 presents calculated particle deflection angles from Eq. (12) as a function of the wave angle γ, and the non-dimensional deflection parameter M. The different M curves in FIG. 5 can represent the effects of power on particle deflection versus wave angle while particle size, fluid compressibility factor, acoustic wavelength, fluid viscosity and fluid velocity are all held constant at a baseline condition. The wave angle variation is from zero to ninety degrees. The particle deflection, at any constant M value, starts at zero where the wave angle is zero and moves up along the forty-five° line until a maximum is reached. Increasing wave angle, with M fixed, increases the component of the radiation force slowing down the particles. At some wave angle condition, the particles are stopped from moving through the waves by the normal radiation force, and are forced by the fluid to move along the wave front direction. At this point, the particle deflection reaches a maximum for that M value (i.e. M=0.667, at a wave angle of 42 degrees is an example).


The triangular solution region under the 45° line shown in FIG. 5 represents all particle deflections possible with a mixture flowing at an angle relative to the bulk acoustic standing waves. It can be applied to any fluid, standing wave, particle or acoustic pressure. It presents particle deflection at all wave angles as a function of a non-dimensional parameter, M, which is the ratio of acoustic radiation force to viscous drag force on the particle. Deflection angles are seen to either fall on, or lie below the 45° line as shown in FIG. 5. The forty-five degree line represents the case where the deflection angle ΔθM and acoustic wave angle γ are equal. This is the maximum particle deflection for any angled acoustic wave and occurs when M/sin γ≥1, i.e., the acoustic radiation force equals or exceeds the viscous drag force. This analytical solution enables angled wave systems to designed and controlled to provide the M values necessary to obtain desired results as discussed in more detail later in this disclosure.


Each M curve in FIG. 5 is seen to have a steep gradient near the maximum deflection value where the particle deflection shifts from the difference between the up and down deflection regions shown in FIG. 1 for a left running wave, to the up deflection only. This steep gradient represents a change in the physical mode of the deflection process and is reflected in the experimental results presented later in this disclosure. This occurs when the radiation force in the upward deflection region reaches a value large enough to stop the particle motion through the wave. The results show that particles flowing in a fluid suspension can be deflected along an acoustic standing wave of any strength, if the wave angle is small enough. The different M curves in FIG. 5 can represent the effects of acoustic pressure on particle deflection versus wave angle while particle size, fluid compressibility factor, acoustic wavelength, fluid viscosity and fluid velocity are all held constant at the baseline condition.


For example, the M=0.8 curve in the figure can represent many different applications. One exemplary application with M=0.8 has a fluid mixture velocity, V=7.75×10−4 m/sec, an acoustic standing wave wavelength, λ=7.4×10−4 m, a mixture viscosity, μ=1.0×10−3 Pa·s, a contrast factor, X=0.12, a mixture compressibility, βf=4.06×10−10 m2/N, particle radius, rp=3×10−6 m, and acoustic pressure amplitude, P0=1.0 MPa as a discussion point. The particle deflection curve presented in FIG. 5 for various M parameters is for all wave angles. Looking at this curve as wave angles are varied from zero to ninety degrees helps interpret the physics. The particle deflection initially moves up the 45° line. Along this line, the particle is stopped between waves, and moves tangentially along the wave front. This effect continues with increasing wave angles until the axial radiation force can no longer stop the normal velocity component of the particle. At this point, the particle moves through multiple waves and is deflected by each wave it passes through. The particle deflection is a maximum of 53°, for M=0.8, at a wave angle of 53°. At a wave angle of 55° with M=0.8, the particle deflection angle drops to 38° and at a wave angle of 60° with M=0.8, the particle deflection is 26.5°.



FIG. 6 presents the particle deflection variation with M that occurs through waves angled at 30°, 45°, and 60°. M is varied from 0 to 1 in FIG. 6. The particle deflection angle ΔθM increases with increasing values of M. The rate of increase of particle deflection angle also grows with increasing values of M. A steep gradient in the deflection curve is observed near the maximum deflection angle for all curves. The magnitude of the gradient is seen to increase with increasing wave angle γ. This steep gradient provides a mechanism for the separation of particles with only slight differences in acoustic properties.



FIGS. 7A, 7B, and 7C present the particle deflection curve versus M for an acoustic wave angle of 45° only. In region 1, the particles pass through all the waves, and get deflected down (for the right running wave shown) at a constant angle, ΔθM smaller than γ as shown in FIG. 7B. The particle net deflection in region 1 is the difference between downward deflection (particle slowed down by the radiation force) and upward deflection (particle accelerated by the radiation force). The curve in FIG. 7A shows the large gradient that occurs when region 1 transitions into region 2. In the vicinity of this transition, a small change in M generates a large change in particle deflection angle ΔθM. The separation of particles with minute size, stiffness or density differences may be accomplished in this transition region. Region 2 presents the operating parameter space where the acoustic radiation force is large enough to stop the particles from moving through the waves. The particles move parallel to the wave front and ΔθM=γ in region 2. Theoretically, in region 2, all the particles will be deflected down the wave front in the first wave as shown in FIG. 7C.


The analytical model results, as presented in FIG. 5, predict that particles in suspension can be deflected down an acoustic standing wave of any strength, if the wave angle is small enough. As the wave angle γ is decreased, the fluid and particle velocity normal to the wave decreases. At some point, the acoustic radiation force will overcome the oncoming particle normal velocity component, and as a result, the particle will stop moving through the wave and will travel along the wave front. This process occurs when the wave angle is low enough to cause the resultant particle velocity component normal to the wave to reach zero. The forty-five degree line in FIG. 5 represents a locus of such points. The analysis predicts the maximum deflection for any value of M always falls on this forty-five degree locus line. Since the acoustic power parameter M is equal to C/V where C represents the maximum particle normal velocity perturbation generated by the acoustic radiation forces, it also can be interpreted as the ΔVN/V where V is the oncoming fluid and particle velocity. When ΔVN=V sin(γ), the acoustic perturbation velocity is equal to the fluid normal velocity component to the wave. Therefore, at any power, or acoustic pressure of the acoustic standing wave, there will be an angle of the standing wave where the radiation force can stop the particle velocity normal to the wave. The following equation defines this point which represents the maximum particle deflection as well as where the deflection curve for a given M value intersects the forty five degree line in FIG. 5:

Δθmax=sin−1(M)=γ  (13)

Equation 13 defines the maximum deflection angle possible, and the wave angle γ needed for maximum particle deflection using angled acoustic standing waves as a function of the non-dimensional parameter M.


The M parameter can also be used to determine the desired operation characteristics, for example, to be used in deflecting extremely small particles in suspension. The smaller the particle size, the lower the M factor. Assuming flow velocity is reduced as low as possible for system feasibility, and power is increased as large as possible, then the M operating curves specify that the system should be operated at as low a wave angle as possible as particle deflection peaks at lower wave angles for low M values. This indicates that systems used with small particles, or nanoparticles, should be operated at extremely small angles (e.g., <5°, <4°, <3°, <2°, <1°).


The predictions presented above are based on analytical procedures for ideal standing waves and fluid velocity fields, and were used as guidance for more accurate numerical particle trajectory studies and experimental verification tests showing the benefits of using acoustic standing waves to deflect, collect, differentiate, separate, purify, or fractionate one population of particles or cells from a mixture that may contain multiple different types of particles, i.e., different in size and/or material properties such as density or compressibility.


The particle trajectory can be solved by numerically integrating the equation of motion of the particle, i.e., Eq. (3) given some initial conditions of the particle. The equation is solved by a fourth order Runge Kutta method with automatic time stepping. In the following results, a uniform velocity profile of fluid for a flow channel of one inch width is used. Typical conditions used in the computations are an acoustic standing wave with a frequency of 2 MHz and an acoustic pressure amplitude of 1 MPa. The acoustic standing wave has a width of one inch and has an angle of 45°.



FIGS. 8A and 8B presents deflection results for a particle with properties that are similar to a Chinese Hamster Ovary (CHO) cell. CHO cells are of interest since they are widely used in the production of recombinant proteins and monoclonal antibodies. A typical CHO cell has a diameter of 18 μm and an acoustic contrast factor of 0.03.



FIGS. 8A and 8B show the numerical particle deflection trajectory for a CHO cell for M/sin γ value less than one and for M/sin γ value greater than one, respectively. The simulation used: a frequency of 2 MHz, an acoustic pressure amplitude of 1 MPa, a CHO cell diameter of 18 μm, and a CHO cell acoustic contrast factor of 0.03. The numerical particle trajectory results further verify the physics of angled standing waves and the analytical predictions presented for two cases, M/sin γ<1 and M/sin γ≥1. These results include inertial effects. Viscosity modifies inertial effects to generate a symmetrical perturbation velocity about the mean normal velocity component which generates the net constant deflection as shown in FIGS. 8A and 8B. Therefore, the particle deflection in the first half wavelengths can vary depending on the exact location of the particle relative to the standing wave, as is shown in FIG. 8 where the initial particle location of the two particles differs by a quarter wavelength in the y direction. The viscosity damps this initial length effect out quickly. The results verify the constant angle of deflection as the particle passes through each half wavelength of the standing wave. When M/sin γ≥1 (i.e., the condition in FIG. 8B), the particle deflection angle equals the standing wave angle. After the initial transient of the particle motion, the particle deflection is along the wave angle.



FIG. 9A shows numerical particle trajectory for CHO cells of diameter 16, 18, and 20 μm and acoustic contrast factor of 0.03. FIG. 9B shows the numerical particle trajectory for CHO cells of diameter 20 μm and acoustic contrast factors of 0.03, 0.035, 0.04, 0.045, and 0.05. The simulation used a frequency of 2 MHz, an acoustic pressure amplitude of 1 MPa, and a velocity amplitude is 6 cm/min.



FIG. 9A shows CHO particle deflections for three slightly different sizes, 16, 18, and 20 μm, representing a size variation of about ±10%. The smallest particle deflection is that of a particle with an M/sin γ value less than one. The 18 μm particle deflects according to an M/sin γ value of less than one but greater than that of the 16 μm particle, resulting in a larger deflection. The 20 μm particles deflection is that of an M/sin γ>1 type trajectory. These small size differences lead to large differences in particle trajectories. FIG. 9B shows similar results but as a function of small changes in acoustic contrast factor, i.e., values of 0.03, 0.035, 0.04, 0.045, and 0.05. These results indicate that angled standing waves can be used to separate, or fractionate particles in suspension by size, acoustic contrast factor, i.e., density and compressibility, and shape. This technique may allow live cells to be separated from dead cells, or even damaged cells from healthy cells. For example, Table 1 presents the acoustic contrast factors for several types of cells.












TABLE 1







Speed of Sound
Acoustic Contrast


Cell Type
Density (g/cc)
(m/s)
Factor


















Jurkat T-cell
1.06
1615
0.079


Primary T-cell
1.04
1560
0.049


Yeast
1.1
1700
0.12


CHO
1.03
1550
0.03










FIG. 10 shows numerical particle trajectories for a CHO cell as a function of velocity magnitude of the fluid through the channel. These particle trajectories verify the effects of normal velocity variation on the particle deflection resulting from a mixture flowing into an acoustic standing wave at an angle of 45°. As the flow velocity increases, A VN/V decreases and particle deflection angles. This effect provides a means to increase the ability to detect minor differences in particle properties by manipulating the fluid velocity. The deflection of the particle by the standing wave can also be controlled and/or amplified by the strength of the acoustic field, the angle of the acoustic field, the properties of the fluid, the three dimensionality of the standing wave, the frequency of the standing wave, the acoustic chamber shape and the mixture flow velocity.



FIG. 11A compares the universal analytical predictions for particle deflection, with numerical particle trajectories over a wide range of M values. The different lines in the figure represent analytical predictions from FIG. 5. The symbols represent numerical data from CFD. Each line or symbol type represents a different M value in FIG. 11. The agreement between analytical predictions and numerical results are good. The errors seen in narrow regions near wave angles of 0°, and 90° are believed to be a result of singularities that occur at these two extremes. The results verify the importance of the deflection parameter M, the location of the maximum deflection, and the existence of a steep gradient region near the maximum deflection point.



FIGS. 11B and 11C present the results of an experiment with an angled wave device that has two outer channels adjacent to a central channel and a wave angle of 45 degrees. The device was operated at a frequency of 2.1 MHz and a flow rate of 2 ml/min in the central channel and 40 ml/min in the outer channels. The outer channels contained clear or buffer fluid, and the central channel was provided with a fluid containing beads of a given size. The power was varied and the deflection angle of the beads versus power was measured and plotted for each of four different groups of beads in FIG. 11B. In addition, as the power was varied, the deflection angle of the beads versus the M factor was measured and plotted for each of four different groups of beads in FIG. 11C. Each of the four different groups of beads had bead sizes falling in a range of sizes that was different for each group of beads. The group denoted with circle shapes in the graph is sized in the range of 10-20 micrometers. The group denoted with triangle shapes in the graph is sized in the range of 27-32 micrometers. The group denoted with diamond shapes in the graph is sized in the range of 32-38 micrometers. The group denoted with square shapes in the graph is sized in the range of 45-53 micrometers. As shown in FIG. 11B, the deflection angle for the beads changed with the change in power. As shown in FIG. 11C, the M factor for all the beads agrees fairly well with the analytical result shown in solid black squares.


The numerical particle trajectory model can easily be modified to take into account more realistic acoustic and flow fields. Computational Fluid Dynamics simulations can be done to determine the fluid velocities in a realistic fluid channel geometry. Similarly, numerical solvers for acoustic fields generated by piezoelectric transducers can be used to predict more accurate solutions for the acoustic field. The particle trajectory model can then make use of the numerically predicted acoustic and fluid velocity fields to obtain more realistic predictions. Another extension is the inclusion of gravitational and buoyancy forces acting on the particles.


Two macroscale, ultrasonic, angled wave separator configurations were fabricated and tested. Two different approaches were used to generate the desired fluid/acoustic interactions. The first concept is that of an Angled Wave Device (AWD) where an angled acoustic standing wave propagates through one or more parallel fluid streams flowing in a straight duct. The second is an Angled Fluid Device (AFD) where narrow fluid streams are injected and controlled to flow through an acoustic standing wave chamber at an angle to the standing wave. These macro scale, ultrasonic separators were shown to have the potential to operate effectively at much higher flow rates and/or at much lower particle concentrations, than conventional acoustic separators. For example, while earlier acoustic separators typically operate a linear velocity of less than 1 mm/s, the systems described in this disclosure can operate at linear velocities of up to 100 mm/s. The test results verified the analytical predictions, and demonstrated the potential to separate, or fractionate particles in suspension by size, density, and speed of sound using angled acoustic standing waves.



FIGS. 12A, 12B, and 12C show an AWD system 100 with a 45° angled standing wave. FIG. 12A is a photograph of the AWD system 100 with multiple flow inlets 110, 112 on the right and multiple flow outlets 114, 116 on the left. FIG. 12B is a schematic of the system 100 showing locations of the transducer 118, reflector 120, and flow channels. FIG. 12C is a schematic illustrating one possible mode of operation of the AWD system 100 with the dash lines representing the nodal plane locations of the standing wave. FIG. 12D is a schematic of the flow profiles within the AWD system 100. FIG. 12E is a cross-section of the AWD system 100 and FIGS. 12F and 12G are cross-sections of alternate duct arrangements for the AWD system.


The AWD system 100 can be operated in horizontal and vertical orientations. Multiple inlets 110, 112 are shown on the right and multiple outlets 114, 116 on the left. The inlet 110 and the inlet 112 are coaxial rectangular ducts with an axis 107. In the orientation shown, the flow travels horizontally from right to left through a flow chamber 109, in this case a rectangular duct. In general, AWD systems include a piezoelectric material configured to be excited to generate an angled acoustic standing wave with a wavelength and an acoustic radiation force in the flow chamber oriented at an acute angle relative to the direction of mean flow through the flow chamber and the flow chamber has a minimum internal dimension that is at least 10 times (e.g., at least 50 times, at least 100 times, or at least 1000 times) the wavelength of the angled acoustic standing wave. In the AWD system 100, an angled standing wave is generated at 45° to the flow direction by a PZT-8, 1 MHz, 1 inch by 1 inch transducer and a stainless steel reflector. Optionally, some systems include multiple transducer/reflector pairs. The minimum internal dimension of the flow chamber 109 of this system is the height 108 of the flow chamber which is about 0.75 inches. In a test described in more detail below, the AWD system 100 was operated vertically with flow downwards to eliminate gravity effects on particle deflections. A mixture of polystyrene beads and water was pumped downward through the 0.2-inch middle inlet channel at a velocity of 155 cm/min. In the AWD system 100, the middle inlet channel (inlet 110) has a cross-sectional area of about 0.15 square inches. In general, AWD systems have mixture inlets with cross-sectional areas of between 0.01 and 2 square inches (e.g., 0.05, 0.1, 0.25, 0.5, 0.75, or 1 square inches).


The space between the ultrasonic transducer and the reflector has a first portion within the flow chamber and a second portion outside the flow chamber. In the acoustic chamber of the AWD system 100, thin acoustically transparent membranes 121 are used to separate the mixture flow from the prismatic void regions (i.e., the second portion outside the flow chamber) set up by the angular transducer and reflector set up. Optionally, the system can include cooling water system in fluid connection with the prismatic void regions. For example, pumps can circulate water through these regions to maintain a constant fluid temperature. In some systems, these prismatic void regions are filled with solid material having an acoustic impedance equivalent to the host fluid. This approach has been found to eliminate flow problems associated with the triangular regions while allowing the angled wave to pass with minimal reflections.


As shown in FIG. 12E, the straight, rectangular duct includes an inner duct (inlet 110) which flows a mixture of particles and a host fluid, and an outer duct (inlet 112) which flows a buffer flow. The buffer flow duct (inlet 110) completely surrounds the mixture flow duct (inlet 112). The mixture flow duct stops before the acoustic region where the acoustic standing wave passes through the system at an angle to the flow direction. The mixture flow duct (outlet 114) is then continued in the rectangular duct system after the acoustic standing wave. As a result, the angled acoustic standing wave passes through both the mixture flow stream and the buffer stream as shown in FIG. 12C. The system amounts to two inlet flows entering the acoustic standing wave and two exit flows leaving the standing wave. The inlet and exit ducts are aligned. The acoustic standing wave is at an angle to the flow direction in the duct.


The flow rates are set to generate laminar flow in the chamber and operate below a Reynolds number of 200 based on equivalent duct diameter. The low Reynolds number results in shear dominated flow, with no turbulence. The flow rate is set in three of the four streams. The two inlet flow rates are set to push the flow, and either outlet flow duct can be set to pull the flow. This push and pull operation assures the flow streams stay laminar and straight, and also provide a means to modify flow profiles for desired particle separation. The average buffer flow velocity can be set above or below the average flow velocity of the mixture flow. As the mixture flow passes through the angled, acoustic standing wave, the particles in suspension will be deflected downward along the wave front as shown. The particle deflection from the horizontal direction can vary from zero up to the wave direction. The deflection is a factor of the M factor. If the M factor is large enough to stop the flow through the waves, the particles will travel along the wave angle. The particles will be carried by the fluid velocity component parallel to the wave. The host fluid direction will be unaffected by the acoustics, and will travel horizontally to the mixture exit duct shown.


Typical velocity profiles through the acoustic section of the AWD system 100 are shown in FIG. 12D. The flow is at an extremely low Reynolds number, which provides shear flow with rapid development in a duct. The flow wants to flow in layers, or laminar flow. This is why at low Reynolds numbers, cylinders have lower drag coefficients than spheres. Three-dimensional regions in the duct shape should be avoided. The inner mixed flow duct should have a high aspect ratio (e.g., of at least 5:1, 10:1, 15:1, 20:1, 25:1, 50:1, 100:1)) such that the mixture duct provides approximately two-dimensional flow for stability. In the AWD system 100, the aspect ratio is about 7:1.


Buffer flow around the duct at the side edges as shown in FIG. 12E is anticipated to limit wall boundary flow effects. No eddies will exist due to viscous dissipation at low Reynolds number. As a result, fully developed, two dimensional laminar flow profiles will develop quickly in the ducts and will enter near the acoustic region in both the mixture duct and the buffer duct as shown. The buffer flow rate is set to allow rapid energizing of the shear layer between the streams thereby providing near constant velocity in the mixture stream flowing through the angled standing wave. The mixture flow duct is terminated well before the acoustic region to allow elimination of the shear layers between the streams as shown in FIG. 12D. In general, the distance di between the inlets and the space between the ultrasonic transducer and the reflector 120 where the angled wave is formed is between 0.025 and 2 (0.5 e.g., 0.05, 0.25, 0.5, 0.75, or 1 inches). In the AWD system 100, the distance di between the inlets and the space between the ultrasonic transducer 118 and the reflector 120 where the angled wave is formed is approximately 0.5 inches.



FIG. 13 is a particle size distribution of polystyrene beads used to test the AWD system 100. The beads used have a mean diameter of about 150 μm and sizes as small as 20 μm and as large as 220 μm. The mixture contained two grams of beads per liter of water. This allowed for visual observation of the mixture flow. A water buffer flow was pumped around and parallel to the mixture at a velocity of 23 cm/min. Electrical power to the transducer was varied from zero to 3.2 Watt (W) and particle deflection was recorded. The wide range of particle size resulted in an even bigger variation of the M parameter. The expectation was that for certain power and fluid velocity, the larger particles will deflect at the 45° wave angle, while the smaller particles would not deflect at all, or at a small angle.



FIGS. 14A-14F are photos of polystyrene beads 122 flowing through the AWD system 100 during the test to show bead deflection as a function of electrical power to the 1 MHz transducer setting up an acoustic standing wave at a 45°. These figures show that bead deflection increased as the power (0 W in FIG. 14A, 0.8 W in FIG. 14B, 1.5 W in FIG. 14C, 1.8 W in FIG. 14D, 2.4 W in FIG. 14E, and 3.2 W in FIG. 14F) was increased. In these photos, the mixture flow is from right to left, gravity forces are right to left, and the acoustic standing wave axial direction is from upper left to lower right in the model window orientation shown. FIG. 14A shows the mixture flow with no acoustics. Without acoustic forces, the beads 122 flow horizontally with the fluid and no particle deflection is observed with the all of the beads flowing to an exit region 123.


The M factor and particle deflection increases directly with electric power supplied to the transducer. The mixture stream was seen to deflect down at an angle less than the wave angle, as it moved through the angled wave from right to left for power up to 1.5 W (see FIG. 14B). At 1.5 W, larger beads started to deflect along the angled wave front while smaller particles traveled straight through the acoustic field, thereby exhibiting fractionation (FIG. 14C). As the power was increased above 1.5 W, medium-sized and smaller-sized beads deflected at the 45° wave angle (FIG. 14D and FIG. 14E), until at 3.2 W, all the visible beads were deflected along the standing wave (FIG. 14F). In addition, the exit region 123 of the smaller beads that were not deflected along the standing wave began to exhibit a gradually increasing deflection as the power increased.


The bead diameter variation was calculated using the M factor based on power variation measured from first noticeable bead deflection to all bead deflection along the wave front. At a power of 1.5 W, the analytical calculations indicated that large particles of 200 μm were deflected along the wave front and a majority of all particles larger than 130 μm were deflected along the wave front at a power of 3.2 W. The analytical prediction is that identical values of the product of the square of particle diameter and acoustic energy, which is proportional to power, yield identical particle deflections. The results agree well with the documented size distribution for the beads and the observed bead behaviour. These test results verify the analytical model, and demonstrate the ability to select and differentiate by size or material property using angled wave technology.


Some AWD systems have a third outlet configured to concentrate material being deflected. For example, these systems can have the second outlet disposed between the first outlet and the third outlet where a cross-sectional area of the third outlet is smaller than a cross-sectional area of the second outlet.



FIGS. 15A and 15B illustrate an AWD system 200 with such duct configuration. The AWD system 200 is configured for concentrating particles or cells by lowering the mixture duct 110 and constricting the lower buffer stream. The outlet mixture duct 114 is attached at the side walls after the flow passes through the acoustic wave to provide particle collection with higher concentrations. This mixture duct attachment is made after the flow passes the acoustic field, allowing buffer flow around the inlet mixture duct 110 before the acoustic wave and thus providing good flow profiles and particle concentration. The duct flow rates can be varied with push/pull mechanisms as described above to help obtain the desired separation and concentration. The mixture duct wall attachment isolates an exit duct 124 from the buffer flow duct (outlet 116). D is the height of the outlet mixture duct 114. h is the height of the buffer flow duct 116 above the mixer duct 114. d is much smaller and is the height of the third outlet duct 124. In the AWD system 200, the width of the ducts is the same. The concentration rate should ideally be D/d if the velocities in both ducts were the same. D/d could be varied accordingly. In AWD systems with this configuration, height D of the outlet mixture duct 114 is generally have between 2 and 100 times the height d of the third outlet wall buffer duct 124 (e.g., 3, 5, 10, 25, 50, 75 times the height d of the third outlet wall buffer duct 124). The mixture to lower buffer flow rate ratio should ideally be D/d if the velocities in both ducts were the same. In the AWD system 200, the height D of the mixture duct 114 is about 3 times the height d of the third outlet 124. The height h of the buffer inlet 112 and buffer outlet 116 can be much smaller than shown in the figure and will be chosen with CFD for specific applications.


Some AWD systems have a plurality of third outlets, each of the plurality of third outlets offset from an axis of the second outlet in a direction of deflection of the angled acoustic wave.



FIG. 16 is a schematic of an AWD system 300 configured for particle fractionation. In the orientation of FIG. 16, the direction of deflection of the angled acoustic wave is downward and the multiple collection ducts 124a-124e are provided below the mixing duct (outlet 114) to collect different size particles. The AWD system 300 has five collection ducts 124a-124e but some AWD systems configured for fractionation have more collection ducts (e.g., 10 collection ducts 15, collection ducts, or 20 collection ducts) or fewer collection ducts (e.g., 4 collection ducts 3, collection ducts, or 2 collection ducts). The M factor is set in Region 1 along with push/pull flow rate settings to provide operation where different deflections occur with different particle sizes. One example configuration has a total system height of one inch with the five collection channels spanning a typical distance of 0.4 inches in total. The system is scalable up or down as needed to accommodate smaller or larger flow rates. Fractionation systems can be used, for example, for cell enrichment from a leukopack (e.g., to fractionate the different cells such as red blood cells, monocytes, granulocytes, and lymphocytes); to fractionate a starting population of T cells according to size; to fractionate an affinity bead/cell complex from unbound free cells; or to fractionate a population of free cells, affinity bead/cell complex A, and affinity bead/cell complex B. Use of the M-factor can aid in design and operation of acoustic separation systems


In one example, a mixed population of two particles of the same material, one of size 5 micron and one of size 10 micron need to be separated in a 45° angled wave device. Operating parameters such as flowrate, power, and frequency are selected such that the M-factor for the bigger particle is M10=0.8. For a 45° angled wave device, this M-factor that results in a particle deflection of 45 degree for the ten-micron particle. Since M scales with the square of the particle radius, the M-factor for the smaller particle is M5=0.8/4=0.2. The deflection angle for this particle is about two degrees. Therefore, a proper angled wave setup with a wave angle of 45° is able to fractionate these two populations.


In a second example, the goal is to fractionate three different cells, lymphocytes, monocytes, and neutrophils, cells found within the white blood cell population. Lymphocytes have a typical size of 6 micron. Monocytes and neutrophils are about ten microns. In addition, the acoustic contrast factor of the lymphocytes is smaller than that of the monocytes. A 45° degree angled wave device can be tuned such that the monocytes have an M-factor of 0.75. The neutrophils being of the same size and slightly smaller acoustic contrast factor have a slightly smaller M-factor of about 0.725. The smaller lymphocytes M-factor scales as ( 6/10)2=0.36, or 36% that of the monocytes, resulting in an M-factor of 0.27. The deflection curve for a 45° wave angle indicates that the monocytes and neutrophils deflect at 45°, whereas the lymphocytes deflect at about 5°. A system with properly designed outlets will be able to harvest separately the monocytes and neutrophils in one channel, and the lymphocytes in a separate outlet, thereby separating and enriching the lymphocytes.


In a third example, the goal is to fractionate the output of an affinity cell selection process. An 25 micron affinity bead is used for a TCR+ T-cell negative cell selection process. The TCR+ T-cells are bound to the affinity bead and form a complex of affinity bead with multiple TCR+ cells attached to the bead. The TCR− T-cells are not bound, remaining in solution as free unbound cells. An angled wave system is then used to fractionate these two populations, free unbound TCR− cells from the affinity bead/TCR+ cell complexes. The radius of the T-cell is about 6 micron. Therefore, the ratio of the M-factor is (25/6)2=17. Choosing system parameters such that the affinity/cell complex has an M-factor of 1 results in the deflection of the complex at the wave angle. The unbound free cell then has an M-factor of 1/17=0.06 which means the free cells deflect at an angle of less than 1°, thereby effectuating a fractionation process of the affinity bead/cell complex from the free cells.


In a fourth example, the goal is to fractionate a mixed cell populations consisting of similar sized cells but with a difference in acoustic contrast factor, with cell A having a contrast factor of 0.03 and cell B having a contrast factor of 0.06. An 45° angled wave system is used to separate cells A from cells B. The system is tuned such that the M-factor of cell B is 0.75, resulting in a deflection of cells B at an angle of 45°. Since the M-factor scales with the contrast factor, the M-factor for cell A is 0.75/2=0.375, resulting in a deflection of about 5 degrees for cell A. A properly designed system should allow for the separation of cells A at 5 degrees from cells B at 45 degrees.



FIGS. 17A, 17B, and 17C are schematics illustrating aspects of an AFD system 400. FIG. 17A shows system geometry and flow characteristics. FIG. 17B shows particle transfer between fluids.



FIG. 17A shows the AFD system 400 with an acoustic chamber which has an ultrasonic transducer 118 on one side, a reflector 120 on the opposite side of the chamber, and multiple flow inlets 110, 112 and outlets 114, 116. The transducer 118 and chamber are designed to generate a bulk, ultrasonic acoustic standing wave traveling horizontally in the chamber as shown n FIG. 17A. The vertical dash lines shown in the figure represent the nodal plane locations of the standing wave. Two inlets 110, 112 are shown in the right top of the chamber, and two outlets 114, 116 are shown at the left bottom of the chamber. A first channel 110′ ends at the first inlet 110 and a second channel 112′ ends at the first inlet 112. The channels 110′, 112′ are at an angle alpha (α) with a plane perpendicular to the angled acoustic standing wave (in the case the horizontal direction) of 60° . In AFD system 400, the first channel 110′ and the second channel 112′ both have a substantially straight section extending at least 0.5 inches from their respective inlet 110, 112.


The two lower exit ducts are at an angle beta (β) with the horizontal of 70°. In some systems, the angles alpha and beta are the same. In some systems, the four ducts all enter the acoustic chamber at different angles. These angles though, will vary between zero and ninety degrees. In some systems, the angle alpha is between 30° and 88° (e.g., more than 35°, more than 40°, more than 45°, more than 50°, more than 55°, more than 60°, less than 80°, less than 75°, less than 70°, less than 65°, less than 60°, less than 55°, less than 50°). In some systems, the angle beta is between 30° and 88° (e.g., more than 35°, more than 40°, more than 45°, more than 50°, more than 55°, more than 60°, less than 80°, less than 75°, less than 70°, less than 65°, less than 60°, less than 55°, less than 50°).


Fluid enters the acoustic chamber through the inlet ducts, and exits the chamber through the exit ducts. Typical duct dimensions are channels depths of 0.5 to 1 inch and channel widths of 0.1 to 0.4 inches. The flow rates are set to generate laminar flow in the chamber and operate below a Reynolds number of 200 based on duct diameter. The low Reynolds number results in shear dominated flow, with no turbulence. The flow rate is set in three of the four ducts attached to the acoustic chamber in FIG. 17A. The flow is both pushed and pulled. The two inlet flow rates are set to push the flow, and the outlet flow carrying the particles is set to pull the flow. This push and pull operation assures the flow streams go where desired. The outlet mixture flow can be set above or below the flowrate entering one of the inlet ducts. Typical flow profiles are shown in the chamber in FIG. 17A. Fully developed laminar flow profiles enter the acoustic chamber as shown. The wall shear layer between at the chamber inlet quickly mix out. A fairly uniform flow develops for a while near the interface of the two injected streams as shown in FIG. 17A. The flow shear forces on the fluid in the corners causes flow rotation, and will generate large scale eddies as shown. This flow rotation will be slow and solid body like rotation because of the low Reynolds number. The flow rates are controlled at both the inlets and the exits. In most of the operations, both inlet duct flow rates will be specified and one of the exit flow ducts will be specified. This type of operation is called push/pull. The acoustic standing wave can be planar, or three dimensional. Planar standing waves are preferred. The wall of the flow chamber adjacent to the first outlet in a direction of deflection of the angled acoustic wave can extend at an acute angle relative to a plane perpendicular to the angled acoustic standing wave. In the AFD system 400, the lower wall of the chamber is tilted down an angle gamma (γ) as shown. This wall slope is designed to help collect particles deflected by acoustic radiation forces. Some AFD systems have wall slopes between 1 and 20 degrees (e.g., more than 2 degrees, more than 3 degrees, more than 5 degrees, more than 10 degrees, less than 15 degrees, less than 10 degrees, less than 7.5 degrees, less than 5 degrees).



FIG. 17B presents the AFD system 400 operating with a fluid mixture with particles in suspension entering through the inlet 110 and clear fluid entering the chamber in the inlet 112. The particles are assumed to have a positive acoustic contrast factor, which means they will deflect towards the nodal plane surfaces as shown. In this manner, all the particles get deflected in the down direction. The angled wall at the bottom of the chamber allows particles to drop out of the acoustic field without getting trapped in the wall shear layer, or held by the acoustic edge effect.



FIG. 17C schematically depicts the fluid flow direction of the AWD system 400. The fluid velocity is decomposed into components normal and tangent to the acoustic standing wave nodal planes. The normal direction represents the axial direction of the standing wave. For a planar wave, this is the direction of the radiation forces on the particles in the mixture. As a result, the radiation forces slow and speed up the normal velocity component of the particles with respect to the fluid normal velocity. The tangential velocity component of the particles remains the same as the fluid. As a result of this effect, the particles are deflected at an angle to the fluid towards the downward direction. If the radiation forces are large enough, the normal velocity of the particle will approach zero, and the particles will move vertically downward while the fluid continues to flow across the chamber towards the exit duct. It is important to realize that these particle deflections use fluid velocity, and more specifically the component of fluid velocity in the downward direction. The fluid carries the particles down. This effect is completely separate from gravity. The process is gravity independent.



FIG. 18A is a photograph of a prototype of the AFD system 400 tested and FIG. 18B is a schematic of the setup showing fluid streamlines from a CFD prediction. In FIG. 18B, the red represents a mixture stream and blue represent a buffer stream. The CFD results show that the flow is regular and uniform without any mixing between the streams. There are two flow inlets 110, 112 and two flow outlets 114, 116 in the AFD system 400. The top inlets are at an angle of 60° with respect to the horizontal direction. The outlets are at 70°. Pumps are used to control both the amount of flow entering the acoustic chamber through the inlets and the flow exiting the outlets (push-pull control). The AFD device was tested with a 1 MHz acoustic standing wave operating at 1 W. The two flow streams make about a 30° angle with the standing wave in the acoustic chamber.



FIGS. 19A and 19B are photographs of the acoustic chamber window of the AFD system showing particle movement through the AFD system without acoustics (FIG. 19A) and with acoustics (FIG. 19B). The test was conducted with 200 ml/min flowing through all inlets and outlets. This results in mixture flow velocities of about 160 cm/min. The mixture stream of polystyrene beads 122 and water is readily visible. The mixture was 2 grams of beads 122 per liter of water. The beads 122 are those described with reference to FIG. 13.


In FIG. 19A (acoustics off), the mixture stream is seen to flow directly from the upper left inlet 110 to the lower left outlet 116 as predicted with CFD. The second stream is water, and it is not visible in the photograph. FIG. 19B (acoustics on) shows the effect of the angled standing waves on the motion of the beads 122. The M/sin(γ) parameter for the test was greater than 1.0. The beads 122 were deflected along the angled wave front almost immediately as they enter the acoustic chamber. This resulted in the vertical motion of all the visible beads 122 from the mixture stream to the buffer stream and down to the bottom of the chamber and into the lower right outlet 114. This result occurs at all buffer flow rates and shows the ability of this system to be used for particle washing, or for particle separation and/or collection at high flow rates when compared to conventional ultrasonic separator systems. The AFD system 400 is not limited to two streams and can be modified to include many different angle variations. The AFD system 400 has the potential to work with a variety of fluid/particle mixtures where the substance in suspension could be beads, cells, exosomes, viruses, oil droplets, or any material that has a different density, compressibility, or contrast factor than the host fluid. The system can work with nanoparticles since the acoustic radiation force effect is amplified by the angle that the flow makes with the acoustic wave.


Some systems are configured to provide fractionation by providing a constriction in the outlet channel positioned to receive deflected material. For example, the fourth channel ending at the second outlet can have a first cross-sectional area. The third channel ending at the first outlet can have a first section with the first cross-sectional area and a second section with a second cross-sectional area that is smaller than the first cross-sectional area with the second section of the third channel located between the first outlet and the first section of the third channel.



FIGS. 20A and 20B illustrates this approach to increasing the concentration of the particle mixture drawn off with AFD systems. In AFD system 500, the lower outlet duct 114 is constricted near the acoustic chamber. This constriction is shown in the particle outlet that is pulled, for example, by a pump to a desired flowrate. Since the flowrate is set by the pull rate, any area constriction results in a velocity increase. The outlet duct constriction d/D increases the flow velocity by D/d for the two dimensional duct shown in FIGS. 20A and 20B. FIG. 20B presents approximate flow profiles for a moderate constriction with a pull flow rate such that the peak velocity in the acoustic chamber occurs in the area near the exit duct constriction region. The higher velocities occurring near the entrance of the exit ducts 114, 116, and near the separation streamline dividing the two flows will provide better separation with fewer particles moving back to the mixture stream. The higher velocities mean higher tangential velocity components to carry the particles (e.g., beads 122) down. As an example, if the flowrates in all four ducts are set the same by the push-pull mode and the constriction is 90% of the duct area, then the velocity near Q4 exit duct entrance will increase ten fold when compared to the second outlet duct flow, Q3, or with respect to the inlet flow of both ducts (Q1 and Q2). This effect is reflected flow profile shown in FIG. 20B. The length of the constriction region shown in the schematic of the velocity profiles provides velocity directions toward the constriction channel. This means less chance of particles re-entering the original mixture stream, and better separation efficiency. In the same configuration, and still assuming a 90% constriction, if the flowrate is set so the Q4 exit duct has one tenth the flow rate of the incoming inlet ducts, the throttled velocity is nearly or exactly the same as the un-throttled exit duct velocity in Q3 and therefore still provides the downward velocity component desired for separating the particles, while flowing much less fluid in exit duct flowrate Q4. This arrangement results in a possible ten times concentration of the mixture with each pass through the AFD separator.



FIG. 21 presents an AFD system 600 designed for particle fractionation. Four inlet ducts 110, 111, 112, 113 and four outlet ducts 114, 115, 116, 118117 are shown. The different shadings represent CFD predictions showing the ability to maintain the four angled streams through the acoustic chamber. Again, push/pull operation allows such unique definition in the acoustic chamber. Some AWD systems include many more streams. All four flows pass though the chamber at an angle to the acoustic standing wave. If the top, or blue stream was a mixture of fluid mixture with multiple particle sizes in suspension, the particles could be fractionated into the lower three collection ducts shown in FIG. 21 using the angled wave deflection process. The system may be operated at an M factor which allows different particles to be deflected for the collection configuration shown. The same AFD system shown in FIG. 21 could be expanded to have five or more inlet ducts and five or more outlet ducts. The incoming mixture and buffer streams could then pass through many different adjacent duct pairs. Operated with push/pull technology, this would allow particle separation with many different wave angles. In the same manner, the different duct streams could be used to set different velocity profiles for different particle separation requirements.



FIGS. 22A, 22B, and 22C are, respectively, a schematic, a plot of modeled flow velocities, and a cross-section of an AFD system 700 designed for particle collection. FIG. 22A shows the flow through the system. The system contains one inlet duct 110 and one outlet duct 116 attached to the acoustic chamber. A collection region 130 is shown below the flow stream passing through the acoustic chamber at an angle to the standing wave as shown. This collection is enhanced by a large scale collection vortex shown in FIG. 22A. This collection vortex is driven by the flow stream passing through the chamber and provides tangential velocity components parallel to the nodal planes which can carry the particles downward out of the mixture stream into the collection regions. The collection vortex can be furthered enhanced by drawing off fluid through the collector outlet 114 at the bottom of system. Turning the acoustics off and on in an appropriate manner to allow particles to fall down to the collection bottom could also enhance performance.



FIGS. 23A and 23B are, respectively, a cross-section and a schematic of a low angle AFD system 700. The M parameter can be used to determine the desired operation characteristics for deflecting extremely small particles (e.g., nanoparticles of the range of 100 nm to 1000 nm or 10 nm to 100 nm, or 1 to 10 nm, bacteria, viruses such as lenti or retro viruses, adeno associated viruses, exosomes, microvesicles, and other nano-sized particles) in suspension. The smaller the particle size, the lower the M factor. In a system with flow velocity reduced as low as possible for system feasibility, and power is increased as large as possible, then the M operating curves specify that the system should be operated at as low a wave angle as possible. Typical operating parameters for these systems are angles between nearly-zero and 15 degrees, frequencies between 2 and 50 MHz, acoustic pressure amplitude between 1 and 20 MPa), and linear velocities are on the order of 10 mm/s, 1 mm/s or 0.1 mm/s. For low M values, deflection peaks at lower wave angles. The AFD system 700 is configured for use with nanoparticles. Two inlet flow ducts 110, 112 feed the acoustic chamber and two exit flow ducts 114, 116 are used to exit the flow streams. Both the inlet angle φi and outlet angle φo are approximately 5°. In other ASWD system, the inlet angle φi and outlet angle φo are different angles (e.g., between 2° and 10°, more than 3°, more than 4°, less than 9°, less than 8°, less than 7°, less than 6°). Again, push/pull techniques can be used to control the flow streams to generate the particle fractionation desired.


The systems and methods described in this disclosure can provide macro-scale, ultrasonic separators that use bulk, acoustic standing waves angled to the direction of a fluid mixture flow field to generate particle deflection that can be used to collect, differentiate, separate, purify, or fractionate one population of particles or cells from a mixture that may contain multiple different types of particles. Particle trajectory equations provide the key physics. The universal prediction curves developed for particle deflection at all wave angles as a function of the non-dimensional parameter M defined by the ratio of acoustic radiation force to viscous drag force on the particle can be used in system design and operation. Particle deflection, measured from the fluid flow direction, varies continuously from zero to a maximum value equal to the wave angle γ, which is the angle that the standing wave makes with the flow direction. The analytical results agreed well with both numerical trajectory computations and model test results. The acoustic pressure amplitude, particle diameter and wave angle were shown to have the largest effect on particle deflection.


Results also showed that for any acoustic pressure amplitude of a standing wave, there is a wave angle of the standing wave where the radiation force stops the particle velocity normal to the wave, and as a result, the particles start to move along the wave front. This point is defined by the non-dimensional parameter M, and angle of the wave γ and operating near this point generates large particle deflection with small changes in controllable parameters such as acoustic power or flow velocity. This operating point is quite useful, since it could allow the separation of particles with minute size, stiffness or density differences.


Some of these systems and methods use standing waves angled to a flow channel or narrow flow streams injected at an angle through a fixed acoustic chamber. Both systems were shown to effectively separate polystyrene beads from a flowing mixture at high speeds when compared to conventional ultrasonic separators. Such macro scale, ultrasonic separators were also shown to effectively operate at much higher flow rates, or at much lower particle concentrations, than conventional acoustic separators. Model test results agreed very well with theory, and verified the prediction system developed. The angled wave system could work with a fluid/substance mixture where the substance in suspension could be micro carrier beads, cells, exosomes, virus, oil, or any material that has a different density, compressibility, or contrast factor than the host fluid. The analytical model predicts that the system can theoretically work even with nanoparticles since the acoustic radiation force effect is amplified by the angle the flow makes with the acoustic wave.



FIGS. 24A-24 C present the results of using an AWD system similar to that shown in FIGS. 12A-12E to fractionate T-cells from 35 um beads. The system had a 30° wave angle and was operated with a frequency of 2.1 MHz and flow rates of 5 ml/min of a T-cell/bead mixture through the center inlet and of 30 ml/min of a buffer through the buffer inlet. FIGS. 24A and 24 B are schematics illustrating the anticipated separation of T-cells from beads. FIG. 24C presents the results. When the system was operated without acoustics, 98% of the T-cells and 95% of the beads flowed through the center outlet. When 2.3 W of power were applied, 92% of the T-cells flowed through the center outlet and 100% of the beads were deflected into the buffer outlet.



FIGS. 25A-25C present the results of using the same AWD system to fractionate a mixed population of beads with sizes mainly 10 um-29 um and 32 um-42 um. The system had a 30° wave angle and was operated with a frequency of 2.1 MHz and flow rates of 2 ml/min of a bead mixture through the center inlet and of 40 ml/min of a buffer through the buffer inlet. The resulting linear flow velocity was 48 cm/min. FIG. 25A is a schematic illustrating the anticipated separation of larger beads from smaller beads. FIGS. 25B and 25C presents the results. When the system was operated without acoustics, most of the beads of both sizes flowed through the center outlet. When 1.5 W of power were applied, most of the smaller beads still flowed through the center outlet but most of the larger beads were deflected into the buffer outlet.



FIGS. 26A-26C present the results of using the same AWD system to fractionate a population of PMMA beads with sizes 5 um-20 um. The system had a 30° wave angle and was operated with a frequency of 2.1 MHz and flow rates of 2 ml/min of a bead mixture through the center inlet and of 40 ml/min of a buffer through the buffer inlet. The resulting linear flow velocity was 48 cm/min. FIG. 26A, 26B, and 26C show the distribution of beads between the center outlet and the buffer outlet without acoustics, with 1W of power applied and with 1.2 W of power applied. When the system was operated without acoustics, most of the beads flowed through the center outlet. When 1 W of power wcro was applied, the larger beads started preferentially being diverted into the buffer outlet. When 1.2 W of power were applied, most of the beads larger than 12 um were deflected into the buffer outlet. These results demonstrate the ability to selectively fractionate material with very small differences.


A number of embodiments of the invention have been described. Nevertheless, it will be understood that various modifications may be made without departing from the spirit and scope of the invention.


For example, FIG. 27 shows a 10-degree AWD system 900 with a center channel and a buffer channel around it. The center channel cross section can be circular or rectangular. A typical cross-section of the system can be from 0.1″×0.1″ to a 1″×1″ channel with a center channel width ranging from ½ to 1/10th of the channel cross-section. Applications include cell fractionation, bead-cell fractionation.


In another example, FIG. 28 shows an AWD system 930 that has one small inlet on a side and buffer flow on top of it and has 5 outlets where different fractions from a mixture population will end up. A typical size of the channel could be from 0.25″×0.25″ to 1″×1″ and relative side inlet width could vary from ½ of the channel width to 1/10th of the channel width. Applications include, for example, leukopack fractionation, T-cell.


In another example, FIG. 29 shows an AWD system 960 in which viewing of the flow is made possible by 2 glass windows. Attachments are included so that the system can be suspended vertically with the help of a metal rod. The angled wave system 960 is the same as the 10-degree AWD system 900. This system can be configured with wave angles between 5 to 85 degrees.


Accordingly, other embodiments are within the scope of the following claims.

Claims
  • 1. A method of separating material from a host fluid, comprising: flowing an initial mixture of the host fluid and the material via an inlet into an acoustophoretic device at a flow rate, the acoustophoretic device including:an acoustic chamber communicating with the inlet;an ultrasonic transducer coupled to the chamber and arranged to be excited to produce a bulk acoustic wave at an angle with a mean direction of flow of the initial mixture;controlling a ratio of acoustic radiation force produced by the ultrasonic transducer and a viscous drag force of the initial mixture to cause a first subgroup of the material passing through the acoustic wave to deflect at an angle that is different than that of a second subgroup of the material, to thereby permit the first and second subgroups to be separated.
  • 2. The method of claim 1, further comprising controlling the ratio by controlling one or more of the angle, the flow rate, a frequency of excitation of the ultrasonic transducer or power supplied to the ultrasonic transducer.
  • 3. The method of claim 2, further comprising controlling the ratio in a range that is determined by characteristics of subgroups of materials in the mixture to be separated.
  • 4. The method of claim 1, further comprising controlling the ratio based on characteristics of one or more subgroups.
  • 5. The method of claim 4, further comprising controlling the ratio based on one or more of material size, density, compressibility or acoustic contrast factor.
  • 6. The method of claim 1, wherein the material further includes a third subgroup that is different from the first subgroup and the second subgroup, and controlling the ratio further comprises causing the third subgroup to deflect at an angle that is different than that of the first subgroup or the second subgroup.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part application of Ser. No. 15/613,790 which is a divisional application of Ser. No. 15/143,481 which claims priority to U.S. Provisional Patent Application Ser. No. 62/316,933, filed on Apr. 1, 2016; and to U.S. Provisional Patent Application Ser. No. 62/154,690, filed on Apr. 29, 2015. This application also claims priority to U.S. Provisional Patent Application Ser. No. 62/479,309, filed on Mar. 30, 2017; and to U.S. Provisional Patent Application Ser. No. 62/485,229, filed on Apr. 13, 2017. All of these applications are incorporated by reference.

US Referenced Citations (479)
Number Name Date Kind
2473971 Ross Jun 1949 A
2667944 Crites Feb 1954 A
3372370 Cyr Mar 1968 A
3555311 Weber Jan 1971 A
4055491 Porath-Furedi Oct 1977 A
4065875 Srna Jan 1978 A
4118649 Schwartzman et al. Oct 1978 A
4125789 Van Schoiack Nov 1978 A
4158629 Sawyer Jun 1979 A
4165273 Azarov et al. Aug 1979 A
4173725 Asai et al. Nov 1979 A
4204096 Barcus et al. May 1980 A
4254661 Kossoff et al. Mar 1981 A
4320659 Lynnworth et al. Mar 1982 A
4344448 Potts Aug 1982 A
4398325 Piaget et al. Aug 1983 A
4484907 Sheeran, Jr. Nov 1984 A
4552669 Sekellick Nov 1985 A
4666595 Graham May 1987 A
4673512 Schram Jun 1987 A
4699588 Zinn et al. Oct 1987 A
4743361 Schram May 1988 A
4759775 Peterson et al. Jul 1988 A
4800316 Wang Jan 1989 A
4821838 Chen Apr 1989 A
4836684 Javorik et al. Jun 1989 A
4860993 Goode Aug 1989 A
4878210 Mitome Oct 1989 A
4983189 Peterson et al. Jan 1991 A
5059811 King et al. Oct 1991 A
5062965 Bernou et al. Nov 1991 A
5085783 Feke et al. Feb 1992 A
5164094 Stuckart Nov 1992 A
5225089 Benes et al. Jul 1993 A
5371429 Manna Dec 1994 A
5395592 Bolleman et al. Mar 1995 A
5431817 Braatz et al. Jul 1995 A
5443985 Lu et al. Aug 1995 A
5452267 Spevak Sep 1995 A
5475486 Paoli Dec 1995 A
5484537 Whitworth Jan 1996 A
5527460 Trampler et al. Jun 1996 A
5560362 Sliwa, Jr. et al. Oct 1996 A
5562823 Reeves Oct 1996 A
5594165 Madanshetty Jan 1997 A
5604301 Mountford et al. Feb 1997 A
5626767 Trampler et al. May 1997 A
5688405 Dickinson et al. Nov 1997 A
5711888 Trampler et al. Jan 1998 A
5831166 Kozuka et al. Nov 1998 A
5834871 Puskas Nov 1998 A
5902489 Yasuda et al. May 1999 A
5912182 Coakley et al. Jun 1999 A
5947299 Vazquez et al. Sep 1999 A
5951456 Scott Sep 1999 A
6090295 Raghavarao et al. Jun 2000 A
6166231 Hoeksema Dec 2000 A
6216538 Yasuda et al. Apr 2001 B1
6205848 Faber et al. Jun 2001 B1
6273262 Yasuda et al. Aug 2001 B1
6332541 Coakley et al. Dec 2001 B1
6391653 Letcher et al. May 2002 B1
6475151 Koger et al. Nov 2002 B2
6482327 Mori et al. Nov 2002 B1
6487095 Malik et al. Nov 2002 B1
6592821 Wada et al. Jul 2003 B1
6641708 Becker et al. Nov 2003 B1
6649069 DeAngelis Nov 2003 B2
6699711 Hahn et al. Mar 2004 B1
6727451 Fuhr et al. Apr 2004 B1
6763722 Fjield et al. Jul 2004 B2
6881314 Wang et al. Apr 2005 B1
6929750 Laurell et al. Aug 2005 B2
6936151 Lock et al. Aug 2005 B1
7008540 Weavers et al. Mar 2006 B1
7010979 Scott Mar 2006 B2
7061163 Nagahara et al. Jun 2006 B2
7081192 Wang et al. Jul 2006 B1
7093482 Berndt Aug 2006 B2
7108137 Lal et al. Sep 2006 B2
7150779 Meegan, Jr. Dec 2006 B2
7186502 Vesey Mar 2007 B2
7191787 Redeker et al. Mar 2007 B1
7322431 Ratcliff Jan 2008 B2
7331233 Scott Feb 2008 B2
7340957 Kaduchak et al. Mar 2008 B2
7373805 Hawkes et al. May 2008 B2
7541166 Belgrader et al. Jun 2009 B2
7601267 Haake et al. Oct 2009 B2
7673516 Janssen et al. Mar 2010 B2
7674630 Siversson Mar 2010 B2
7837040 Ward et al. Nov 2010 B2
7846382 Strand et al. Dec 2010 B2
7968049 Takahashi et al. Jun 2011 B2
8075786 Bagajewicz Dec 2011 B2
8080202 Takahashi et al. Dec 2011 B2
8134705 Kaduchak et al. Mar 2012 B2
8256076 Feller Sep 2012 B1
8266950 Kaduchak et al. Sep 2012 B2
8273253 Curran Sep 2012 B2
8273302 Takahashi et al. Sep 2012 B2
8309408 Ward et al. Nov 2012 B2
8319398 Vivek et al. Nov 2012 B2
8334133 Fedorov et al. Dec 2012 B2
8387803 Thorslund et al. Mar 2013 B2
8592204 Lipkens et al. Nov 2013 B2
8679338 Rietman et al. Mar 2014 B2
8691145 Dionne et al. Apr 2014 B2
8873051 Kaduchak et al. Oct 2014 B2
8889388 Wang et al. Nov 2014 B2
9272234 Lipkens et al. Mar 2016 B2
9357293 Claussen May 2016 B2
9365815 Miyazaki et al. Jun 2016 B2
9368110 Hershey et al. Jun 2016 B1
9388363 Goodson et al. Jul 2016 B2
9391542 Wischnewskiy Jul 2016 B2
9403114 Kusuura Aug 2016 B2
9410256 Dionne et al. Aug 2016 B2
9416344 Lipkens et al. Aug 2016 B2
9421553 Dionne et al. Aug 2016 B2
9422328 Kennedy, III et al. Aug 2016 B2
9457139 Ward et al. Oct 2016 B2
9457302 Lipkens et al. Oct 2016 B2
9458450 Lipkens et al. Oct 2016 B2
9464303 Burke Oct 2016 B2
9476855 Ward et al. Oct 2016 B2
9480375 Marshall et al. Nov 2016 B2
9480935 Mariella, Jr. et al. Nov 2016 B2
9488621 Kaduchak et al. Nov 2016 B2
9504780 Spain et al. Nov 2016 B2
9512395 Lipkens et al. Dec 2016 B2
9513205 Yu et al. Dec 2016 B2
9514924 Morris et al. Dec 2016 B2
9517474 Mao et al. Dec 2016 B2
9532769 Dayton et al. Jan 2017 B2
9533241 Presz, Jr. et al. Jan 2017 B2
9550134 Lipkens et al. Jan 2017 B2
9550998 Williams Jan 2017 B2
9556271 Blumberg et al. Jan 2017 B2
9556411 Lipkens et al. Jan 2017 B2
9566352 Holmes et al. Feb 2017 B2
9567559 Lipkens et al. Feb 2017 B2
9567609 Paschon et al. Feb 2017 B2
9572897 Bancel et al. Feb 2017 B2
9573995 Schurpf et al. Feb 2017 B2
9574014 Williams et al. Feb 2017 B2
9580500 Schurpf et al. Feb 2017 B2
9587003 Bancel et al. Mar 2017 B2
9597357 Gregory et al. Mar 2017 B2
9597380 Chakraborty et al. Mar 2017 B2
9605074 Shah Mar 2017 B2
9605266 Rossi et al. Mar 2017 B2
9606086 Ding et al. Mar 2017 B2
9608547 Ding et al. Mar 2017 B2
9611465 Handa et al. Apr 2017 B2
9616090 Conway et al. Apr 2017 B2
9623348 McCarthy et al. Apr 2017 B2
9629877 Cooper et al. Apr 2017 B2
D787630 Lipkens et al. May 2017 S
9644180 Kahvejian et al. May 2017 B2
9645060 Fiering May 2017 B2
9656263 Laurell et al. May 2017 B2
9657290 Dimov et al. May 2017 B2
9662375 Jensen et al. May 2017 B2
9663756 Lipkens et al. May 2017 B1
9670477 Lipkens et al. Jun 2017 B2
9670938 Beliavsky Jun 2017 B2
9675668 Bancel et al. Jun 2017 B2
9675902 Lipkens et al. Jun 2017 B2
9675906 Lipkens et al. Jun 2017 B2
9677055 Jones et al. Jun 2017 B2
9685155 Hershey et al. Jun 2017 B2
9686096 Lipkens et al. Jun 2017 B2
9688958 Kennedy, III et al. Jun 2017 B2
9689234 Gregory et al. Jun 2017 B2
9689802 Caseres et al. Jun 2017 B2
9695063 Rietman et al. Jul 2017 B2
9695442 Guschin et al. Jul 2017 B2
9810665 Fernald et al. Nov 2017 B2
9833763 Fernald et al. Dec 2017 B2
9869659 Buckland et al. Jan 2018 B2
9872900 Ciaramella et al. Jan 2018 B2
9873126 Mao et al. Jan 2018 B2
9873894 Conway et al. Jan 2018 B2
9878056 Bancel et al. Jan 2018 B2
9878536 Foresti et al. Jan 2018 B2
9879087 DeSander et al. Jan 2018 B2
9990297 Conway et al. Jan 2018 B2
9907846 Morein et al. Mar 2018 B2
9908288 Harkness Mar 2018 B2
9909117 Kaduchak Mar 2018 B2
9909313 Grubbs Mar 2018 B1
9913656 Stulen Mar 2018 B2
9913866 O'Shea et al. Mar 2018 B2
9925277 Almarsson et al. Mar 2018 B2
9926382 Fischer et al. Mar 2018 B2
9937207 Gregory et al. Apr 2018 B2
9938390 Storti et al. Apr 2018 B2
9943599 Gehl et al. Apr 2018 B2
9944702 Galetto Apr 2018 B2
9944709 Galetto Apr 2018 B2
9994743 El-Zahab Apr 2018 B2
9974898 Spain et al. May 2018 B2
20020038662 Schuler et al. Apr 2002 A1
20020134734 Campbell et al. Sep 2002 A1
20030015035 Kaduchak et al. Jan 2003 A1
20030028108 Miller et al. Feb 2003 A1
20030195496 Maguire Oct 2003 A1
20030209500 Kock et al. Nov 2003 A1
20030230535 Affeld et al. Dec 2003 A1
20040016699 Bayevsky Jan 2004 A1
20040035208 Diaz et al. Feb 2004 A1
20040057866 Zumeris et al. Mar 2004 A1
20040112841 Scott Jun 2004 A1
20040124155 Meegan, Jr. Jul 2004 A1
20040149039 Cardelius Aug 2004 A1
20050031499 Meier Feb 2005 A1
20050121269 Namduri Jun 2005 A1
20050145567 Quintel et al. Jul 2005 A1
20050196725 Fu Sep 2005 A1
20050239198 Kunas Oct 2005 A1
20060037915 Strand et al. Feb 2006 A1
20060037916 Trampler Feb 2006 A1
20060050615 Swisher Mar 2006 A1
20070053795 Laugharn, Jr. et al. Mar 2007 A1
20070138108 Hadfield et al. Jun 2007 A1
20070224676 Haq Sep 2007 A1
20070267351 Roach et al. Nov 2007 A1
20070272618 Gou et al. Nov 2007 A1
20070284299 Xu et al. Dec 2007 A1
20080011693 Li et al. Jan 2008 A1
20080067128 Hoyos et al. Mar 2008 A1
20080105625 Rosenberg et al. May 2008 A1
20080181838 Kluck Jul 2008 A1
20080217259 Siversson Sep 2008 A1
20080245709 Kaduchak et al. Oct 2008 A1
20080245745 Ward et al. Oct 2008 A1
20080264716 Kuiper et al. Oct 2008 A1
20080272034 Ferren et al. Nov 2008 A1
20080272065 Johnson Nov 2008 A1
20080316866 Goodemote et al. Dec 2008 A1
20090029870 Ward et al. Jan 2009 A1
20090042253 Hiller et al. Feb 2009 A1
20090048805 Kaduchak et al. Feb 2009 A1
20090053686 Ward et al. Feb 2009 A1
20090087492 Johnson et al. Apr 2009 A1
20090098027 Tabata et al. Apr 2009 A1
20090104594 Webb Apr 2009 A1
20090126481 Burris May 2009 A1
20090178716 Kaduchak et al. Jul 2009 A1
20090194420 Mariella, Jr. et al. Aug 2009 A1
20090227042 Gauer et al. Sep 2009 A1
20090045107 Ward et al. Dec 2009 A1
20090295505 Mohammadi et al. Dec 2009 A1
20100000945 Gavalas Jan 2010 A1
20100078323 Takahashi et al. Apr 2010 A1
20100078384 Yang Apr 2010 A1
20100124142 Laugharn et al. May 2010 A1
20100139377 Huang et al. Jun 2010 A1
20100192693 Mudge et al. Aug 2010 A1
20100193407 Steinberg et al. Aug 2010 A1
20100206818 Leong et al. Aug 2010 A1
20100255573 Bond et al. Oct 2010 A1
20100261918 Chianelli et al. Oct 2010 A1
20100317088 Radaelli et al. Dec 2010 A1
20100323342 Gonzalez Gomez et al. Dec 2010 A1
20100330633 Walther et al. Dec 2010 A1
20110003350 Schafran et al. Jan 2011 A1
20110024335 Ward et al. Feb 2011 A1
20110092726 Clarke Apr 2011 A1
20110095225 Eckelberry et al. Apr 2011 A1
20110123392 Dionne et al. May 2011 A1
20110125024 Mueller May 2011 A1
20110146678 Ruecroft et al. Jun 2011 A1
20110154890 Holm et al. Jun 2011 A1
20110166551 Schafer Jul 2011 A1
20110189732 Weinand et al. Aug 2011 A1
20110207225 Mehta et al. Aug 2011 A1
20110245750 Lynch et al. Oct 2011 A1
20110262990 Wang et al. Oct 2011 A1
20110278218 Dionne et al. Nov 2011 A1
20110281319 Swayze et al. Nov 2011 A1
20110309020 Rietman et al. Dec 2011 A1
20120088295 Yasuda et al. Apr 2012 A1
20120145633 Polizzotti et al. Jun 2012 A1
20120161903 Thomas et al. Jun 2012 A1
20120163126 Campbell et al. Jun 2012 A1
20120175012 Goodwin et al. Jul 2012 A1
20120231504 Niazi Sep 2012 A1
20120267288 Chen et al. Oct 2012 A1
20120325727 Dionne et al. Dec 2012 A1
20120325747 Reitman et al. Dec 2012 A1
20120328477 Dionne et al. Dec 2012 A1
20120329122 Lipkens et al. Dec 2012 A1
20130017577 Arunakumari et al. Jan 2013 A1
20130115664 Khanna et al. May 2013 A1
20130175226 Coussios et al. Jul 2013 A1
20130206688 El-Naas Aug 2013 A1
20130217113 Srinivasan et al. Aug 2013 A1
20130277316 Dutra et al. Oct 2013 A1
20130277317 LoRicco et al. Oct 2013 A1
20130284271 Lipkens et al. Oct 2013 A1
20130316412 Schultz et al. Nov 2013 A1
20140011240 Lipkens et al. Jan 2014 A1
20140017758 Kniep et al. Jan 2014 A1
20140102947 Baym et al. Apr 2014 A1
20140141413 Laugham, Jr. et al. May 2014 A1
20140154795 Lipkens et al. Jun 2014 A1
20140319077 Lipkens et al. Oct 2014 A1
20140329997 Kennedy, III et al. Nov 2014 A1
20140377834 Presz, Jr. et al. Dec 2014 A1
20150053561 Ward et al. Feb 2015 A1
20150060581 Santos et al. Mar 2015 A1
20150252317 Lipkens et al. Sep 2015 A1
20150274550 Lipkens et al. Oct 2015 A1
20150321129 Lipkens et al. Nov 2015 A1
20160060615 Walther et al. Mar 2016 A1
20160089620 Lipkens et al. Mar 2016 A1
20160102284 Lipkens et al. Apr 2016 A1
20160121331 Kapur et al. May 2016 A1
20160123858 Kapur et al. May 2016 A1
20160145563 Berteau et al. May 2016 A1
20160153249 Mitri Jun 2016 A1
20160175198 Warner et al. Jun 2016 A1
20160184790 Sinha et al. Jun 2016 A1
20160202237 Zeng et al. Jul 2016 A1
20160208213 Doyle et al. Jul 2016 A1
20160230168 Kaduchak et al. Aug 2016 A1
20160237110 Gilmanshin et al. Aug 2016 A1
20160237394 Lipkens et al. Aug 2016 A1
20160237395 Lipkens et al. Aug 2016 A1
20160252445 Yu et al. Sep 2016 A1
20160279540 Presz, Jr. et al. Sep 2016 A1
20160279551 Foucault Sep 2016 A1
20160287778 Leach Oct 2016 A1
20160312168 Pizzi Oct 2016 A1
20160314868 El-Zahab et al. Oct 2016 A1
20160319270 Lipkens et al. Nov 2016 A1
20160325039 Leach et al. Nov 2016 A1
20160325206 Presz, Jr. et al. Nov 2016 A1
20160332159 Dual et al. Nov 2016 A1
20160339360 Lipkens et al. Nov 2016 A1
20160347628 Dionne et al. Dec 2016 A1
20160355776 Lipkens et al. Dec 2016 A1
20160361670 Lipkens et al. Dec 2016 A1
20160363579 Lipkens et al. Dec 2016 A1
20160368000 Dionne et al. Dec 2016 A1
20160369236 Kennedy, III et al. Dec 2016 A1
20160370326 Kaduchak et al. Dec 2016 A9
20170000413 Clymer et al. Jan 2017 A1
20170002060 Bolen et al. Jan 2017 A1
20170002839 Burkland et al. Jan 2017 A1
20170007679 Maeder et al. Jan 2017 A1
20170008029 Lipkens et al. Jan 2017 A1
20170016025 Poirot et al. Jan 2017 A1
20170016027 Lee et al. Jan 2017 A1
20170020926 Mata-Fink et al. Jan 2017 A1
20170029802 Lipkens et al. Feb 2017 A1
20170035866 Poirot et al. Feb 2017 A1
20170037386 Jones et al. Feb 2017 A1
20170038288 Ward et al. Feb 2017 A1
20170042770 Warner et al. Feb 2017 A1
20170044517 Lipkens et al. Feb 2017 A1
20170049949 Gilmanshin et al. Feb 2017 A1
20170056448 Glick et al. Mar 2017 A1
20170058036 Ruiz-Opazo et al. Mar 2017 A1
20170065636 Moriarty et al. Mar 2017 A1
20170066015 Lipkens et al. Mar 2017 A1
20170067021 Moriarty et al. Mar 2017 A1
20170067022 Poirot et al. Mar 2017 A1
20170072405 Mao et al. Mar 2017 A1
20170073406 Schurpf et al. Mar 2017 A1
20170073423 Juillerat et al. Mar 2017 A1
20170073638 Campana et al. Mar 2017 A1
20170073684 Rossi et al. Mar 2017 A1
20170073685 Maeder et al. Mar 2017 A1
20170080070 Weinschenk et al. Mar 2017 A1
20170080423 Dauson et al. Mar 2017 A1
20170081629 Lipkens et al. Mar 2017 A1
20170088809 Lipkens et al. Mar 2017 A1
20170088844 Williams Mar 2017 A1
20170089826 Lin Mar 2017 A1
20170096455 Baric et al. Apr 2017 A1
20170107536 Zhang et al. Apr 2017 A1
20170107539 Yu et al. Apr 2017 A1
20170119820 Moriarty et al. May 2017 A1
20170128523 Ghatnekar et al. May 2017 A1
20170128857 Lipkens et al. May 2017 A1
20170130200 Moriarty et al. May 2017 A1
20170136168 Spain et al. May 2017 A1
20170137491 Matheson et al. May 2017 A1
20170137774 Lipkens et al. May 2017 A1
20170137775 Lipkens et al. May 2017 A1
20170137802 Lipkens et al. May 2017 A1
20170145094 Galetto May 2017 A1
20170151345 Shah Jun 2017 A1
20170152502 Scharenberg et al. Jun 2017 A1
20170152503 Scharenberg et al. Jun 2017 A1
20170152504 Scharenberg et al. Jun 2017 A1
20170152505 Scharenberg et al. Jun 2017 A1
20170152527 Paschon et al. Jun 2017 A1
20170152528 Zhang et al. Jun 2017 A1
20170158749 Cooper et al. Jun 2017 A1
20170159005 Lipkens et al. Jun 2017 A1
20170159007 Lipkens et al. Jun 2017 A1
20170166860 Presz, Jr. et al. Jun 2017 A1
20170166877 Bayle et al. Jun 2017 A1
20170166878 Thanos et al. Jun 2017 A9
20170166903 Zhang et al. Jun 2017 A1
20170173080 Lee et al. Jun 2017 A1
20170173128 Hoge et al. Jun 2017 A1
20170173498 Lipkens et al. Jun 2017 A9
20170175073 Lipkens et al. Jun 2017 A1
20170175125 Welstead et al. Jun 2017 A1
20170175139 Wu et al. Jun 2017 A1
20170175144 Zhang et al. Jun 2017 A1
20170175509 Abdel-Fattah et al. Jun 2017 A1
20170175720 Tang et al. Jun 2017 A1
20170183390 Springer et al. Jun 2017 A1
20170183413 Galetto Jun 2017 A1
20170183418 Galetto Jun 2017 A1
20170183420 Gregory et al. Jun 2017 A1
20170184486 Mach et al. Jun 2017 A1
20170189450 Conway et al. Jul 2017 A1
20170190767 Schurpf et al. Jul 2017 A1
20170191022 Lipkens et al. Jul 2017 A1
20170232439 Suresh et al. Aug 2017 A1
20170374730 Flores Dec 2017 A1
20180000311 Lipkens et al. Jan 2018 A1
20180000870 Britt Jan 2018 A1
20180000910 Chakraborty et al. Jan 2018 A1
20180008707 Bussmer et al. Jan 2018 A1
20180009158 Harkness et al. Jan 2018 A1
20180009888 Baumeister et al. Jan 2018 A9
20180009895 Smith et al. Jan 2018 A1
20180010085 Lipkens et al. Jan 2018 A1
20180010117 Paschon et al. Jan 2018 A1
20180014846 Rhee Jan 2018 A1
20180015128 Britt Jan 2018 A1
20180015392 Lipkens et al. Jan 2018 A1
20180016570 Lipkens et al. Jan 2018 A1
20180016572 Tang Jan 2018 A1
20180020295 Pander et al. Jan 2018 A1
20180021379 Galetto et al. Jan 2018 A1
20180022798 Shurpf et al. Jan 2018 A1
20180028683 Wong et al. Feb 2018 A1
20180043473 Helvajian et al. Feb 2018 A1
20180049767 Gee et al. Feb 2018 A1
20180051089 Galettto et al. Feb 2018 A1
20180051265 Cooper Feb 2018 A1
20180052095 Cumbo et al. Feb 2018 A1
20180052147 Zeng Feb 2018 A1
20180055529 Messerly et al. Mar 2018 A1
20180055530 Messerly et al. Mar 2018 A1
20180055531 Messerly et al. Mar 2018 A1
20180055532 Messerly et al. Mar 2018 A1
20180055997 Cabrera et al. Mar 2018 A1
20180056095 Messerly et al. Mar 2018 A1
20180057810 Zhang et al. Mar 2018 A1
20180058439 Locke et al. Mar 2018 A1
20180066223 Lim Mar 2018 A1
20180066224 Lipkens et al. Mar 2018 A1
20180066242 Zhang Mar 2018 A1
20180067044 Kaduchak et al. Mar 2018 A1
20180071363 Ghatnekar et al. Mar 2018 A1
20180071981 Collino et al. Mar 2018 A1
20180078268 Messerly Mar 2018 A1
20180080026 Rossi et al. Mar 2018 A1
20180085743 Yavorsky et al. Mar 2018 A1
20180087044 Lipkens et al. Mar 2018 A1
20180088083 Sinha Mar 2018 A1
20180092338 Hering et al. Apr 2018 A1
20180092660 Houser et al. Apr 2018 A1
20180094022 Bracewell et al. Apr 2018 A1
20180095067 Huff et al. Apr 2018 A1
20180098785 Price et al. Apr 2018 A1
20180100134 Lim Apr 2018 A1
20180100204 O'Shea Apr 2018 A1
20180130491 Mathur May 2018 A1
Foreign Referenced Citations (148)
Number Date Country
2002236405 Sep 2002 AU
105 087 788 Nov 2015 CN
104722106 Apr 2016 CN
30 27 433 Feb 1982 DE
32 18 488 Nov 1983 DE
196 48 519 Jun 1998 DE
103 19 467 Jul 2004 DE
10 2008 006 501 Sep 2008 DE
10 2014 206 823 Oct 2015 DE
0 292 470 Nov 1988 EP
0 167 406 Jul 1991 EP
0 641 606 Mar 1995 EP
1 175 931 Jan 2002 EP
1 254 669 Nov 2002 EP
1 308 724 May 2003 EP
2 209 545 Jul 2010 EP
270152 Jan 2018 EP
2419511 Jan 2018 EP
3068888 Jan 2018 EP
3257600 Jan 2018 EP
3274453 Jan 2018 EP
3274454 Jan 2018 EP
3275894 Jan 2018 EP
278108 Feb 2018 EP
3279315 Feb 2018 EP
3286214 Feb 2018 EP
2289535 Mar 2018 EP
2545068 Mar 2018 EP
2675540 Mar 2018 EP
2750683 Mar 2018 EP
2796102 Mar 2018 EP
3066201 Mar 2018 EP
3066998 Mar 2018 EP
3107552 Mar 2018 EP
3288660 Mar 2018 EP
3288683 Mar 2018 EP
3289362 Mar 2018 EP
3291842 Mar 2018 EP
3291852 Mar 2018 EP
3292142 Mar 2018 EP
3292195 Mar 2018 EP
3292515 Mar 2018 EP
3294343 Mar 2018 EP
3294764 Mar 2018 EP
3294857 Mar 2018 EP
3294871 Mar 2018 EP
3294888 Mar 2018 EP
3294896 Mar 2018 EP
3296302 Mar 2018 EP
3297740 Mar 2018 EP
3298046 Mar 2018 EP
3164488 Apr 2018 EP
3301115 Apr 2018 EP
3302783 Apr 2018 EP
3302789 Apr 2018 EP
3303558 Apr 2018 EP
3306310 Apr 2018 EP
2 420 510 May 2006 GB
9-136090 May 1997 JP
1442486 Sep 2014 KR
2037327 Jun 1995 RU
2085933 Jul 1997 RU
629496 Oct 1978 SU
WO 198707178 Dec 1987 WO
WO 8911899 Dec 1989 WO
WO 9005008 Mar 1990 WO
WO 9501214 Jan 1995 WO
WO 9734643 Sep 1997 WO
WO 1998017373 Apr 1998 WO
WO 9850133 Nov 1998 WO
WO 0041794 Jul 2000 WO
WO 02072234 Sep 2002 WO
WO 02072236 Sep 2002 WO
WO 03089567 Oct 2003 WO
WO 2004079716 Sep 2004 WO
WO 2009063198 May 2009 WO
WO 2009111276 Sep 2009 WO
WO 2009144709 Dec 2009 WO
WO 2010024753 Apr 2010 WO
WO 2010040394 Apr 2010 WO
WO 2011023949 Mar 2011 WO
WO 2011025890 Mar 2011 WO
WO 2011027146 Mar 2011 WO
WO 2011131947 Oct 2011 WO
WO 2011161463 Dec 2011 WO
WO 2013043044 Mar 2013 WO
WO 2013043297 Mar 2013 WO
WO 2013049623 Apr 2013 WO
WO 2013055517 Apr 2013 WO
WO 2013138797 Sep 2013 WO
WO 2013148376 Oct 2013 WO
WO 2013159014 Oct 2013 WO
WO 2014014941 Jan 2014 WO
WO 2014029505 Feb 2014 WO
WO 2014046605 Mar 2014 WO
WO 2014055219 Apr 2014 WO
WO 2014124306 Aug 2014 WO
WO 2014153651 Oct 2014 WO
WO 2015006730 Jan 2015 WO
WO 2015102528 Jul 2015 WO
WO 2016004398 Jan 2016 WO
WO 2016124542 Aug 2016 WO
WO 2016176663 Nov 2016 WO
WO 2016209082 Dec 2016 WO
WO 2017041102 Mar 2017 WO
WO 20174201349 Nov 2017 WO
WO 2017218714 Dec 2017 WO
WO 2018009894 Jan 2018 WO
WO 2018002036 Jan 2018 WO
WO 2018005873 Jan 2018 WO
WO 2018013558 Jan 2018 WO
WO 2018013629 Jan 2018 WO
WO 2018013840 Jan 2018 WO
WO2018014174 Jan 2018 WO
WO2018015561 Jan 2018 WO
WO 20180011600 Jan 2018 WO
WO2018018958 Feb 2018 WO
WO2018021920 Feb 2018 WO
WO2018022158 Feb 2018 WO
WO2018022513 Feb 2018 WO
WO2018022619 Feb 2018 WO
WO2018022651 Feb 2018 WO
WO2018022930 Feb 2018 WO
WO2018023114 Feb 2018 WO
WO2018024639 Feb 2018 WO
WO2018026644 Feb 2018 WO
WO2018026941 Feb 2018 WO
WO2018028647 Feb 2018 WO
WO 2018034343 Feb 2018 WO
WO2018034885 Feb 2018 WO
WO 2018035141 Feb 2018 WO
WO 2018035423 Feb 2018 WO
WO20180202691 Feb 2018 WO
WO2018034655 Mar 2018 WO
WO 2018038711 Mar 2018 WO
WO 2018039119 Mar 2018 WO
WO 2018039407 Mar 2018 WO
WO 2018039408 Mar 2018 WO
WO 2018039410 Mar 2018 WO
WO 2018039412 Mar 2018 WO
WO 2018039515 Mar 2018 WO
WO 2018045284 Mar 2018 WO
WO 2018049226 Mar 2018 WO
WO 2018050738 Mar 2018 WO
WO 2018057825 Mar 2018 WO
WO 2018063291 Apr 2018 WO
WO 2018081476 May 2018 WO
WO 20180814701 May 2018 WO
Non-Patent Literature Citations (81)
Entry
Ding et al., Cell separation using tilted-angle standing surface acoustic waves, Sep. 9, 2014, PNAS, vol. 111, No. 36, pp. 12992-12997 (Year: 2014).
Rogers et al., Exploitation of surface acoustic waves to drive size-dependent microparticle concentration within a drop, 2010, Lab Chip, 10, 2979-2985, (Year: 2010).
Barnkob et al., Acoustic radiation- and streaming-inducted microparticle velocities determined by microparticle image velocimetry in an ultrasound symmetry plane), 2012, Physical Review E, 86, pp. 056307-1 to 056307-11 (Year: 2012).
Alvarez et al.; Shock Waves, vol. 17, No. 6, pp. 441-447, 2008.
Augustsson et al., Acoustophoretic microfluidic chip for sequential elution of surface bound molecules from beads or cells, Biomicrofluidics, Sep. 2012, 6(3):34115.
Benes et al.; Ultrasonic Separation of Suspended Particles, 2001 IEEE Ultrasonics Symposium; Oct. 7-10, 2001; pp. 649-659; Atlanta, Georgia.
Castilho et al.; Animal Cell Technology: From Biopharmaceuticals to Gene Therapy; 11—Animal Cell Separation; 2008.
Castro; Tunable gap and quantum quench dynamics in bilayer graphene; Jul. 13, 2010; Mathematica Summer School.
Chitale et al.; Understanding the Fluid Dynamics Associated with Macro Scale Ultrasonic Separators; Proceedings of Meetings on Acoustics, May 2015.
Cravotto et al.; Ultrasonics Sonochemistry, vol. 15, No. 5, pp. 898-902, 2008.
Garcia-Lopez, et al; Enhanced Acoustic Separation of Oil-Water Emulsion in Resonant Cavities. The Open Acoustics Journal. 2008, vol. 1, pp. 66-71.
Grenvall et al.; Concurrent Isolation of Lymphocytes and Granulocytes Using Prefocused Free Flow Acoustophoresis; Analytical Chemistry; vol. 87; pp. 5596-5604; 2015.
Higginson et al.; Tunable optics derived from nonlinear acoustic effects; Journal of Applied Physics; vol. 95; No. 10; pp. 5896-5904; 2004.
Hill et al.; Ultrasonic Particle Manipulation; Microfluidic Technologies for Miniaturized Analysis Systems, Jan. 2007, pp. 359-378.
Ilinskii et al.; Acoustic Radiation Force on a Sphere in Tissue; AIP Conference Proceedings; 2012.
Kuznetsova et al.; Microparticle concentration in short path length ultrasonic resonators: Roles of radiation pressure and acoustic streaming; Journal of the Acoustical Society of America, American Institute of Physics for the Acoustical Society of America, vol. 116, No. 4, Oct. 1, 2004, pp. 1956-1966, DOI: 1.1121/1.1785831.
Latt et al.; Ultrasound-membrane hybrid processes for enhancement of filtration properties; Ultrasonics sonochemistry 13.4 (2006): 321-328.
Li et al.; Electromechanical behavior of PZT-brass unimorphs; J. Am. Ceram. Soc. vol. 82; No. 7; pp. 1733-1740, 1999.
Lipkens et al.; The effect of frequency sweeping and fluid flow on particle trajectories in ultrasonic standing waves; IEEE Sensors Journal, vol. 8, No. 6, pp. 667-677, 2008.
Lipkens et al.; Frequency sweeping and fluid flow effects on particle trajectories in ultrasonic standing waves; Acoustics 08, Paris, Jun. 29-Jul. 4, 2008.
Lipkens et al.; Prediction and measurement of particle velocities in ultrasonic standing waves; J. Acoust. Soc. Am., 124 No. 4, pp. 2492 (A) 2008.
Lipkens et al.; Separation of micron-sized particles in macro-scale cavities by ultrasonic standing waves; Presented at the International Congress on Ultrasonics, Santiago; Jan. 11-17, 2009.
Lipkens et al.; Separation of bacterial spores from flowering water in macro-scale cavities by ultrasonic standing waves; submitted/uploaded to http://arxiv.org/abs/1006.5467 on Jun. 28, 2010.
Lipkens et al., Macro-scale acoustophoretic separation of lipid particles from red blood cells, The Journal of the Acoustical Society of America, vol. 133, Jun. 2, 2013, p. 045017, XP055162509, New York, NY.
Meribout et al.; An Industrial-Prototype Acoustic Array for Real-Time Emulsion Layer Detection in Oil Storage Tanks; IEEE Sensors Journal, vol. 9, No. 12, Dec. 2009.
Musiak et al.; Design of a Control System for Acoustophoretic Separation, 2013 IEEE 56th International Midwest Symposium on Circuits and Systems (MWSCAS), Aug. 2013, pp. 1120-1123.
Nilsson et al.; Review of cell and particle trapping in microfluidic systems; Department of Measurement Technology and Industrial Electrical Engineering, Div. of Nanobiotechnology, Lund University, P.O. Box 118. Lund, Sweden, Analytica Chimica Acta 649, Jul. 14, 2009, pp. 141-157.
Pangu et al.; Droplet transport and coalescence kinetics in emulsions subjected to acoustic fields; Ultrasonics 46, pp. 289-302 (2007).
Phys. Org. “Engineers develop revolutionary nanotech water desalination membrane.” Nov. 6, 2006. http://phys.org/news82047372.html.
Ponomarenko et al.; Density of states and zero Landau level probed through capacitance of graphene; Nature Nanotechnology Letters, Jul. 5, 2009; DOI: 10.1038/NNANO.2009.177.
“Proceedings of the Acoustics 2012 Nantes Conference,” Apr. 23-27, 2012, Nantes, France, pp. 278-282.
Ryll et al.; Performance of Small-Scale CHO Perfusion Cultures Using an Acoustic Cell Filtration Device for Cell Retention: Characterization of Separation Efficiency and Impact of Perfusion on Product Quality; Biotechnology and Bioengineering; vol. 69; Iss. 4; pp. 440-449; Aug. 2000.
Seymour et al, J. Chem. Edu., 1990, 67(9), p. 763, published Sep. 1990.
Volpin et al.; Mesh simplification with smooth surface reconstruction; Computer Aided Design; vol. 30; No. 11; 1998.
Wang et al.; Retention and Viability Characteristics of Mammalian Cells in an Acoustically Driven Polymer Mesh; Biotechnol. Prog. 2004, pp. 384-387 (2004).
Wicklund et al.; Ultrasonic Manipulation of Single Cells; Methods in Molecular Biology; vol. 853; pp. 1777-196; 2012.
Annex to Form PCT/ISA/206—Communication Relating to the Results of the Partial International Search Report dated Jul. 18, 2013.
European Search Report of European Application No. 11769474.5 dated Sep. 5, 2013.
European Search Report of European Application No. 11796470.0 dated Jan. 5, 2016.
European Search Report of European Application No. 13760840.2, dated Feb. 4, 2016.
European Search Report of European Application No. 13721179.3 dated Mar. 23, 2016.
European Search Report for European Application No. 14749278.9 dated Jan. 13, 2017.
Extended European Search Report for European Application No. EP 12833859.7 dated Mar. 20, 2015.
Extended European Search Report for European Application No. EP 14787587.6 dated Jan. 2, 2017.
International Search Report and Written Opinion for International Application No. PCT/US2011/032181 dated Dec. 20, 2011.
International Search Report and Written Opinion for International Application No. PCT/US2011/040787 dated Feb. 27, 2012.
International Search Report and Written Opinion for International Application No. PCT/US2012/051804 dated Nov. 16, 2012.
International Search Report and Written Opinion for International Application No. PCT/US2013/037404 dated Jun. 21, 2013.
International Search Report and Written Opinion for International Application No. PCT/US2013/032705 dated Jul. 26, 2013.
International Search Report and Written Opinion for International Application No. PCT/US2013/050729 dated Sep. 25, 2013.
International Search Report and Written Opinion for International Application No. PCT/US2013/059640 dated Feb. 18, 2014.
International Search Report and Written Opinion for International Application No. PCT/US2014/015382 dated May 6, 2014.
International Search Report and Written Opinion for International Application No. PCT/US2014/035557 dated Aug. 27, 2014.
International Search Report and Written Opinion for International Application No. PCT/US2014/043930 dated Oct. 22, 2014.
International Search Report and Written Opinion for International Application No. PCT/US2014/046412 dated Oct. 27, 2014.
International Search Report and Written Opinion for International Application No. PCT/US2014/064088 dated Jan. 30, 2015.
International Search Report and Written Opinion for International Application No. PCT/US2015/010595 dated Apr. 15, 2015.
International Search Report and Written Opinion for International Application No. PCT/US2015/019755 dated May 4, 2015.
International Search Report and Written Opinion for International Application No. PCT/US2015/030009 dated Jul. 30, 2015.
International Search Report and Written Opinion for International Application No. PCT/US2015/039125 dated Sep. 30, 2015.
International Search Report and Written Opinion for International Application No. PCT/US2015/053200 dated Dec. 28, 2015.
International Search Report and Written Opinion for International Application No. PCT/US2015/066884, dated Mar. 22, 2016.
International Search Report and Written Opinion for International Application No. PCT/US2016/024082 dated Jun. 27, 2016.
International Search Report and Written Opinion for International Application No. PCT/US2016/031357 dated Jul. 26, 2016.
International Search Report and Written Opinion for International Application No. PCT/US2016/038233 dated Sep. 26, 2016.
International Search Report and Written Opinion for International Application No. PCT/US2015/024365 dated Oct. 13, 2016.
International Search Report and Written Opinion for International Application No. PCT/US2016/041664 dated Oct. 18, 2016.
International Search Report and Written Opinion for International Application No. PCT/US2016/044586 dated Oct. 21, 2016.
International Search Report and Written Opinion for International Application No. PCT/US2016/049088 dated Nov. 28, 2016.
International Search Report and Written Opinion for International Application No. PCT/US2016/050415 dated Nov. 28, 2016.
International Search Report and Written Opinion for International Application No. PCT/US2016/037104 dated Dec. 16, 2016.
International Search Report and Written Opinion for International Application No. PCT/US2017/015197 dated Apr. 3, 2017.
International Search Report and Written Opinion for International Application No. PCT/US2017/015450 dated Apr. 10, 2017.
International Search Report and Written Opinion for International Application No. PCT/US2016/047217 dated Apr. 11, 2017.
International Search Report and Written Opinion for International Application No. PCT/US2016/048243 dated Apr. 20, 2017.
International Search Report and Written Opinion for International Application No. PCT/US2017/017788 dated May 8, 2017.
International Search Report and Written Opinion for International Application No. PCT/US2017/030903 dated Jul. 19, 2017.
International Search Report and Written Opinion for International Application No. PCT/US2017/025108 dated Jul. 20, 2017.
International Search Report and Written Opinion for International Application No. PCT/US2017/031425 dated Aug. 30, 2017.
Sony New Release: <http://www.sony.net/SonyInfo/News/Press/201010/10-137E/index.html>.
International Search Report and Written Opinion for International Application No. PCT/US2017/031425 dated Oct. 23, 2017.
Related Publications (1)
Number Date Country
20180298371 A1 Oct 2018 US
Provisional Applications (4)
Number Date Country
62316933 Apr 2016 US
62154690 Apr 2015 US
62479309 Mar 2017 US
62485229 Apr 2017 US
Divisions (1)
Number Date Country
Parent 15143481 Apr 2016 US
Child 15613790 US
Continuation in Parts (1)
Number Date Country
Parent 15613790 Jun 2017 US
Child 15942316 US