Christopher M Boyce1, Daniel J Holland1, Stuart A Scott2, John S Dennis1. 1. Department of Chemical Engineering and Biotechnology, University of Cambridge , New Museums Site, Pembroke Street, Cambridge CB2 3RA, U.K. 2. Department of Engineering, University of Cambridge , Cambridge CB2 1PZ, U.K.
Abstract
Discrete element modeling is being used increasingly to simulate flow in fluidized beds. These models require complex measurement techniques to provide validation for the approximations inherent in the model. This paper introduces the idea of modeling the experiment to ensure that the validation is accurate. Specifically, a 3D, cylindrical gas-fluidized bed was simulated using a discrete element model (DEM) for particle motion coupled with computational fluid dynamics (CFD) to describe the flow of gas. The results for time-averaged, axial velocity during bubbling fluidization were compared with those from magnetic resonance (MR) experiments made on the bed. The DEM-CFD data were postprocessed with various methods to produce time-averaged velocity maps for comparison with the MR results, including a method which closely matched the pulse sequence and data processing procedure used in the MR experiments. The DEM-CFD results processed with the MR-type time-averaging closely matched experimental MR results, validating the DEM-CFD model. Analysis of different averaging procedures confirmed that MR time-averages of dynamic systems correspond to particle-weighted averaging, rather than frame-weighted averaging, and also demonstrated that the use of Gaussian slices in MR imaging of dynamic systems is valid.
Discrete element modeling is being used increasingly to simulate flow in fluidized beds. These models require complex measurement techniques to provide validation for the approximations inherent in the model. This paper introduces the idea of modeling the experiment to ensure that the validation is accurate. Specifically, a 3D, cylindrical gas-fluidized bed was simulated using a discrete element model (DEM) for particle motion coupled with computational fluid dynamics (CFD) to describe the flow of gas. The results for time-averaged, axial velocity during bubbling fluidization were compared with those from magnetic resonance (MR) experiments made on the bed. The DEM-CFD data were postprocessed with various methods to produce time-averaged velocity maps for comparison with the MR results, including a method which closely matched the pulse sequence and data processing procedure used in the MR experiments. The DEM-CFD results processed with the MR-type time-averaging closely matched experimental MR results, validating the DEM-CFD model. Analysis of different averaging procedures confirmed that MR time-averages of dynamic systems correspond to particle-weighted averaging, rather than frame-weighted averaging, and also demonstrated that the use of Gaussian slices in MR imaging of dynamic systems is valid.
Despite the widespread
practical importance of fluidized beds,
the underlying physics of these systems is still not well understood.[1] This lack of understanding is due in part to
the fact that the flows in fluidized beds are difficult to measure
because the beds are opaque. Consequently, nonintrusive measurement
techniques such as magnetic resonance (MR) imaging, should ideally
be employed. Additionally, granular matter in fluidized beds can possess
gas-, liquid-, and solid-like properties,[2] making it very difficult to model accurately. To predict the behavior
of fluidized beds, two characteristics must be modeled properly: (1)
the contact forces between the particles, and (2) the interaction
forces between the particles and the fluid. The difficulties in measuring
and modeling fluidized beds potentially lead to experimental results
and simulations with a combination of known and unknown inaccuracies.
Thus, to cross-validate these models and measurements, it is important
to compare their results in as direct a manner as possible. Here,
a 3D bubbling fluidized bed has been investigated because it provides
a challenging system exhibiting unsteady flow of fluid and particles
with regions both dense and sparse in particle contacts.With
the drastic increase in computational power in the past few
decades, computational modeling of fluidized beds has become more
widespread. An accurate model is advantageous because it can provide
insight into aspects such as particle mixing, particle velocity, and
bubble formation and complement experimental investigations. Currently,
two forms of computational models dominate the modeling of laboratory-scale
fluidized beds: discrete element modeling with computational fluid
dynamics (DEM-CFD) and two-fluid modeling (TFM). The main difference
between DEM-CFD and TFM is that a DEM-CFD treats particles as individual
objects governed by Newtonian physics, while TFM considers the particles
as a continuous phase governed by continuum mechanics. The main advantage
of TFM over DEM-CFD is that it can model larger beds. However, DEM-CFD
can provide more detailed and accurate results since aspects of individual
particles such as location and velocity can be monitored, and DEM-CFD
does not require the introduction of parameters such as particle “viscosity”
and “pressure”. The main imperfection in DEM-CFD is
that it does not resolve fluid flow on the subparticle level, and
thus requires a drag law to describe the fluid–particle interaction
forces needed to close the momentum equations for both phases. Direct
numerical simulation (DNS) could resolve fluid flow on a subparticle
level, and thus use the no-slip boundary condition instead of a drag
law to model fluid–particle interaction more accurately. However,
DNS is too computationally expensive to model laboratory-scale fluidized
beds. To illustrate the computational requirements of DEM-CFD, a standard
desktop computer will simulate, in one day, approximately one second
of the fluidization of 30 000 particles. For the same run time on
the same computer, a system simulated using DNS would have to be roughly
10 times smaller in volume and number of particles, and a system simulated
using TFM could be roughly 10 times bigger.[3]A prerequisite for relying on the predictions of a discrete
element
model is to validate it by experiment. Several experimental techniques
such as X-ray imaging, diffusive wave spectroscopy (DWS), particle
image velocimetry (PIV), positron emission particle tracking (PEPT),
magnetic resonance (MR), and electrical capacitance tomography (ECT)
have been used to study various aspects of fluidized beds. MR is especially
powerful because it can be used noninvasively to study 3D opaque systems
at fine temporal and spatial resolution and does not require tracer
particles. It has been used for investigation of a variety of aspects
of fluidized beds[4−7] and has also proved useful in validating numerical simulations of
complex flows.[8−11] However, MR measurements are produced in the Fourier domain and
the effect of the MR sampling strategy, which is determined by the
pulse sequence and postprocessing methods used, can be complicated
when used to study dynamic systems such as fluidized beds. For example,
many MR studies of fluidization have presented information on time-averaged
properties, yet the method for time averaging employed by MR can be
vastly different from a naive notion of time averaging. This issue
will be investigated in the present work.To date, several comparisons
have been made between discrete element
models and experimental measurements of phenomena in fluidized beds.[12−21] These studies have largely been conducted on 2D rectangular beds
and have focused on varying DEM-CFD parameters including the drag
law used,[12,13] numerical implementation of fluid–particle
interaction force,[14] contact parameters,[15−19] grid size on a 2D rectangular fluid grid[12] and wall boundary conditions.[13,15,18,19] Generally, there tend to be significant
discrepancies between DEM-CFD and experimental results, even after
optimization of the DEM-CFD parameters. As a result, the assumption
has been that the DEM-CFD is not representing, fully, the physics
of the fluidized system. However, surprisingly little has been done
to investigate whether the results from DEM-CFD simulations and those
from experiments have been sampled and processed in the same way so
as to give a direct comparison. Thus, the present investigation is
concerned with comparing results from a novel 3D cylindrical discrete
element model with experimental results, varying the ways in which
the DEM-CFD results were sampled and processed, rather than varying
the input parameters to the DEM-CFD. Accordingly, the objectives were
(1) to examine how the averaging technique used in the postprocessing
of DEM-CFD data affected the output, and (2) to process the results
predicted by a discrete element model in a manner similar to that
used in MR imaging, thereby investigating the correspondence between
the averaging and slice selection techniques used in model and experiment.
Methods
Experiment
The
experimental results
were those of Holland et al.,[6] and the
reader is referred there for a detailed explanation of the experimental
arrangement. The fluidized bed was contained in an acrylic tube (i.d.
44 mm, o.d. 60 mm) and the particles were rhoeas poppy seeds (Sutton
Seeds, UK). The rhoeas seeds were 1.2 mm in diameter with an apparent
density of ∼900 kg m–3, giving a minimum
fluidization velocity (Umf) of 0.3 m s–1 at ambient conditions. Sufficient particles were
used to give a 30 mm settled bed height. The distributor was a porous
glass frit 40 mm in diameter and the bed was fluidized by humidified
air, with flow rate controlled by an Omega FMA5443 mass flow controller.
The pressure drop across the distributor was typically between 500
and 2100 Pa, and always greater than the pressure drop across the
bed (∼200 Pa).The pulse sequence used by Holland et
al.[5] was the phase-encoded velocity imaging
sequence shown in Figure 1: the motion was
encoded in the phase of the observed complex signal using a sine-shaped,
motion-encoding gradient. A Cartesian coordinate system was employed,
with the z-axis aligned along the vertical, axial,
direction. The spatial resolution in the velocity measurements was
1.04 mm in the vertical (z) direction by 0.94 mm
in the horizontal (x) direction (misquoted as 1.25
mm × 0.73 mm by Holland et al.[6]).
Particles were selectively refocused using a soft radio frequency
pulse, forming slices 5 mm thick in the y-direction
for imaging in the x-z plane, shown
schematically in Figure 2. These slices were
achieved by manipulating the pulse sequence such that the MR signal
from the particles was weighted with a Gaussian distribution based
on the position of the particles in the horizontal y-direction. The Gaussian distribution was set such that the MR signal
in the center of the bed in the y-direction was weighted
most heavily, with the signal originating 2.5 mm from the center in
the y-direction weighted 1/10th as much as that coming
from the center. A diagram of the Gaussian slices used in this experiment
as compared to “top hat” slices with 5 mm thickness
is shown in Figure 2. The sine gradient was
applied with a half period, δ, of 0.56 ms and the observation
time, Δ, was 2 ms for the velocity measurements. To obtain a
time-averaged image of the velocity, 48 averages of signal maps in k-space were acquired; the time between the start of successive
pulse sequences, the recovery time, was 250 ms, making the total acquisition
time ∼30 min.
Figure 1
Pulse sequence modeled for MR-type postprocessing of time
averaged
axial velocity measurements. (Reproduced with permission from ref (6). Copyright 2008 Elsevier).
The flow gradients were applied in the z-direction
for axial velocity measurement. The slice gradient was modeled in
the y-direction to produce an image in the xz plane. The read and phase gradients were applied in the x and z directions, respectively. The phase
gradient was cycled through randomly to simulate the randomness in
consecutive MR imaging excitations with regard to the passage of bubbles.
MR signal data was recorded during the positive portion of the read
gradient with the spin echo occurring at the midpoint of the readout.
Figure 2
Plot of 5 mm y-slice in fluidized
bed (left).
Plot of Gaussian and top-hat signal weighting functions versus y-position in the fluidized bed (right).
Pulse sequence modeled for MR-type postprocessing of time
averaged
axial velocity measurements. (Reproduced with permission from ref (6). Copyright 2008 Elsevier).
The flow gradients were applied in the z-direction
for axial velocity measurement. The slice gradient was modeled in
the y-direction to produce an image in the xz plane. The read and phase gradients were applied in the x and z directions, respectively. The phase
gradient was cycled through randomly to simulate the randomness in
consecutive MR imaging excitations with regard to the passage of bubbles.
MR signal data was recorded during the positive portion of the read
gradient with the spin echo occurring at the midpoint of the readout.Plot of 5 mm y-slice in fluidized
bed (left).
Plot of Gaussian and top-hat signal weighting functions versus y-position in the fluidized bed (right).
Simulations
The
same fluidized bed
experiment was simulated computationally. The motion for each particle
in the simulated fluidized bed was governed by a model developed from
that of Müller et al.,[13] based on
a technique originally developed by Tsuji et al.[22] This technique combines a discrete element model[23] to simulate particle motion with computational
fluid dynamics of the volume-averaged Navier–Stokes equations
derived by Anderson and Jackson.[24] Thus,
the particles are modeled individually, with Newtonian physics and
contact mechanics governing their motion, while fluid is modeled as
a continuum with properties calculated at discrete locations on a
fluid grid. The technique was adapted to simulate a cylindrical fluidized
bed in which the computational fluid dynamics was modeled in cylindrical
coordinates while the motion of the particles was modeled in rectangular
coordinates. A paper presenting a complete description of the computational
model has recently been submitted for publication.[25]The normal contact force on each particle was determined
using a Hertzian model, while the tangential contact force was determined
using the model of Tsuji et al.,[26] in which
Coulomb’s law was introduced to account for sliding. Particle
and fluid motion were stepped forward explicitly in time using the
third order Adams–Bashforth scheme. An explicit scheme was
used to allow for pressure waves to travel through the system for
future studies of pressure oscillations in fluidized beds, and the
third order Adams–Bashforth scheme was used to increase simulation
accuracy and stability as compared with first- and second-order time
stepping techniques.The fluid motion was modeled using computational
fluid dynamics
on a cylindrical grid, invoking volume-averaged Navier–Stokes
equations[24] to account for portions of
fluid cells being occupied by particles. To keep fluid control volumes
of constant volume, a methodology was developed in which length of
the control volumes in the radial direction was kept constant, yet
the angle subtended by fluid control volumes decreased with the distance
of the control volumes from the center. A horizontal cross section
of the fluid grid used in this model is shown in Figure 3. The force of interaction between fluid and particles was
modeled using the drag law developed by Beetstra et al.,[27] chosen because it matched experimental results
better than other drag laws in a previous comparison between a DEM-CFD
simulation and experimental results.[12]
Figure 3
Horizontal
cross section of a novel CFD grid. Different colors
denote different CFD cells. More CFD cells are used in the annuli
further from the center, such that the fluid cells have a constant
volume to ensure the same accuracy in the volume-averaged fluid equations.
Horizontal
cross section of a novel CFD grid. Different colors
denote different CFD cells. More CFD cells are used in the annuli
further from the center, such that the fluid cells have a constant
volume to ensure the same accuracy in the volume-averaged fluid equations.As noted earlier, the fluidized
bed simulated was that used experimentally
by Holland et al.,[6] thereby allowing a
direct comparison between model and experiment. The bubbling bed was
fluidized at twice the minimum fluidization velocity (2Umf), as determined experimentally by Holland et al.[6] This was confirmed by the predictions of the
DEM-CFD of the plot of pressure drop across the bed versus superficial
velocity; further details of fluidization parameters are given in
Table 1. The time step for the particles was
chosen such that it would be 1/20th of a typical collision time between
particles in this system in order to ensure each collision would be
accurately simulated. The parameters for particle contacts are shown
in Table 2, and were chosen on the basis of
the analysis of Müller et al.[13] for
modeling the poppy seeds used in MR experiments. The initial conditions
and boundary conditions for the fluid are shown in Table 3. For the CFD grid, the inlet velocity in the outer
annulus of fluid cells next to the distributor was set proportionally
lower than the inlet velocity for the inner annuli of fluid cells
to account for, as accurately as possible, the fact that, in the magnetic
resonance experiments, a 40 mm diameter distributor was used in a
44 mm diameter tube, with no inlet flow occurring between radii of
20 and 22 mm. At the outlet, a 3D characteristic boundary condition[28] was used for the momentum and continuity equations,
in order to ensure that pressure waves could freely exit the system
without being reflected back into it. The specifications of the cylindrical
fluid grid used in the model are detailed in Table 4.
Table 1
Physical Setup of the Fluidized Bed
System Simulated Using DEM-CFD
parameter
value
height
of settled bed
30 mm
diameter of bed
44 mm
diameter of particles
1.2 mm
density of particles
900 kg/m3
Geldart group
D
Umf
0.3 m/s
U/Umf
2.0
number of particles
30 250
Table 2
Parameters Used for
Discrete Element
Model of Contacts between Particles
parameter
value
coefficient
of sliding friction
0.1
Young’s
modulus
1.2 × 108 Pa
Poisson’s ratio
0.33
normal damping coefficient
0.02
tangential damping coefficient
0.0001
time step
1.25 × 10–6 s
Table 3
Conditions Imposed for Computational
Fluid Dynamics in DEM-CFD Simulation
aspect of simulation
condition imposed
fluid-particle interaction
Beetstra et al.
(2007) correlation
fluid type
compressible
time stepping scheme
explicit 3rd order Adams-Bashforth
initial pressure
105 Pa
initial velocity
0.0 m/s
inlet
velocity
inner 4 annuli: 1.83 m/s
outer annulus: 0.89 m/s
inlet voidage
0.4
boundary velocity
full-slip
temperature
298.15 K
Table 4
Sizing of Fluid Grid and Voidage Grid
Used in DEM-CFD Simulation
parameter
value
fluid
grid radial spacing (dr)
4.4 mm
number of inner radial
control volumes
5
fluid grid
vertical spacing (dz)
5 mm
number of inner vertical
control volumes
23
number of angular control volumes
inner annulus: 4
2nd annulus: 12
3rd annulus:
20
4th annulus: 28
5th annulus: 36
voidage grid horizontal
spacing (dx,dy)
2.2 mm
voidage grid vertical
spacing (dz)
4 mm
Turbulence
modeling was not included for modeling the fluid. The
Reynolds number for the system was 1900 based on the bed diameter,
and 80 based on the interstices between particles. At this Re, the effects of turbulence were expected to be small,
due to the large inertia of the particles as well as the fact that
the turbulence would be dampened by viscous forces imparted on the
fluid by the particles.[29] While some work
has been conducted to implement turbulence modeling in DEM-CFD models,[30−33] it is very difficult to implement turbulence models in a way which
properly accounts for the effect of particles, and thus has largely
been applied for modeling more dilute systems with higher Re.[30−32]
Postprocessing of the DEM-CFD
Results
DEM-CFD results were analyzed in three ways to determine
the time-averaged
particle velocity in each voxel of a map in the x–z plane: (1) a frame-based average in which velocities were averaged,
irrespective of the number of particles in the voxels, (2) a particle-weighted
average, in which the velocity was averaged based on the number of
particles in the voxel, and (3) a Fourier-domain average mimicking
the MR-imaging acquisition process. Each of these approaches is explained
below:
Frame-Based Averaging
The positions
and velocities of particles were processed at instants in time separated
by 10 ms intervals to determine time-averaged particle velocities
using frame-based averaging. The frame-based method averaged velocities
captured at different instants or “frames” in time,
with equal weighting given to each frame:Here, vavg,(x, z) is the frame-based
average particle velocity in the voxel centered about the point (x, z), Nframes is the number of frames used to calculate the average. The velocity vavg,(x, z) is the average particle velocity in voxel (x,z) at time k, defined bywhere n(x,z)
is the number of particles in the voxel at instant k and v is the corresponding velocity of particle l in the voxel. A particle was considered to be entirely inside voxel
(x,z) if it its center resided inside
the limits of the voxel. The weighting function for each particle’s
velocity, w, is based on the position of a particle in the y-direction, y, to account for the fact that the time-averaged velocity is
only desired for a thin slice through the fluidized bed in the y-direction, rather than the entire bed. The only weighting
function studied for frame-based averaging was a “top-hat”
function, as shown in Figure 2. With this weighting
function, particles are weighted by a function which depends on their
position in the y-direction, shown in Figure 2. With the top hat function, only particles between y = −2.5 mm and y = +2.5 mm were
counted; those outside the region were not, so that:where y is the y-coordinate of
particle l at instant k. Furthermore,
frame-based averaging is divided into two categories, “frame
1” and “frame 2″, which correspond to potential
experimental procedures which read velocity signals from particles
differently; these procedures could correspond to, for example, different
time-averaging methods for particle imaging velocimetry (PIV) data.
In the “frame 1” methodology, a frame is not counted
toward the final number of frames for a particular voxel if there
are no particles in the voxel at that instant in time. In “frame
2″, a frame is counted as having a velocity of zero if there
are no particles in the voxel at that instant in time.
Particle-Based Averaging
In particle-based
averaging, the time-averaged velocity map is weighted by the number
of particles which pass through a voxel over the averaging time interval,
rather than averaging over a number of time instants. Thus,With a top-hat
weighting function, the difference
between particle- and frame-based time-averaging can be illustrated
as follows. In particle-based averaging, if a particular voxel at
a particular frame in time contains two particles, it will count twice
as much toward the time average as a different frame in time when
the voxel only contains one particle. In frame-based averaging, the
average velocity in the voxel from these two frames contributes equally
toward the final average.Two additional weighting functions
were used for particle-based averaging. First, a Gaussian function
was used, as shown in Figure 2. The standard
deviation, σ = 1.165 mm, was chosen such that the value 2.5
mm from the center was one-tenth of that at the center:The standard deviation was varied in a later
analysis to examine the sensitivity of the results to slice thickness.
Second, an analysis was made for volume-based, particle-based averaging
with a Gaussian weighting function:where V is the
volume of particle l. Since the experimental MR images
were based on raw measurements
of particles weighted by both a Gaussian function and the volume of
the particles, the averaging procedure of eq 6 was expected to most closely match MR averages.
Processing of DEM-CFD Results to Match the
Acquisition and Processing of Raw MR Imaging Measurements
Practical complications make it impossible for any experimental technique
to follow exactly any of the basic averaging procedures for obtaining
a time-averaged velocity laid out in the previous section. MR imaging
is expected to follow a particle-based average with Gaussian slice
weighting; however, for a variety of reasons it is unclear to what
extent an MR imaging measurement will differ from a pure particle-based
average. Aspects such as (a) sampling Fourier coefficients at different
times over a long acquisition time, (b) imperfections in gradient
ramping, (c) motion encoding arising from the image encoding gradients,
(d) inability to register properly a distribution of particle velocities,
and (e) signal decay during individual readouts could all contribute
to artifacts and deviations from a pure particle-based average. Instead,
results from the DEM-CFD were processed in a manner simulating the
acquisition process of an MR experiment.The particle positions
from DEM-CFD results were used to simulate MR signals from the particles
throughout the pulse sequence. The simulated signal was then processed
by Fourier transformation to yield a time-averaged particle velocity
image, as if it were an experimental result from a phase-encoded MR
velocity determination. To simulate the excitation indicated by the
black bar in Figure 1, each particle was given
a signal density, ρ, proportional to its volume. The signal
from each particle then varied over the course of the pulse sequence
depending on its position while different magnetic gradients were
applied to the system, according towhere S(t) is the
simulated MR signal from particle i at time t in the pulse sequence, ρ is its signal density, and ω is the
frequency at which the nuclear spins inside the particle precess at
time t. The frequency ω was determined by the
particle’s position and the gradients in the magnetic field,
according towhere γ = 2.675 × 108 rad/(s/T) is the gyromagnetic
ratio of 1H nuclei in the
oil in the particles, G is the three-dimensional vector
describing the applied magnetic gradients and r is the
position vector of the center of a particle. To reduce computational
demand in postprocessing, each particle was approximated as a point
located at r. Figure 1 shows the
sequence of r.f. pulses and magnetic gradients used in the experimental
MR imaging and modeled in the MR-type postprocessing of the DEM-CFD
results. Particle positions from the DEM-CFD simulations were recorded
every 10 μs for 3.38 ms to model a full MR pulse sequence. The
flow-encoding gradient, Gflow, was applied
to ensure that particle velocity was imaged, rather than just particle
position; this gradient consisted of two sinusoidal lobes separated
in time and was applied in the axial (z) direction
to ensure axial velocity was imaged. The read gradient was applied
in the x-direction, as an x–z plane velocity image was desired; during the 640 μs-long positive
portion of the read gradient, 64 samplings of the signal from each
particle were taken at different points in k space to contribute to the signal map.The total acquisition time of the experimental measurements was
30 min. It was not possible to simulate this length of time numerically,
therefore a strategy was devised to mimic the experimental acquisition
as best as possible. Three approaches were used:(1) The number
of averages was reduced from 48 to 32. Experimentally,
the number of averages was determined by the required signal-to-noise
ratio (SNR). The simulations are essentially noise free and therefore
a reduced number of averages is justified.(2) The same measurements
of particle motion were used for the
positive, negative and zero flow encoding gradients.(3) Each
excitation was initiated every 10 ms instead of every
250 ms. The reduced sampling time primarily affected the phase encoding.
Phase encoding was applied in the z-direction and
the magnitude of Gphase determined the
value of k sampled for
each simulated excitation. In experimental MR imaging, the phase gradients
are incremented methodically between excitations, from −32ΔGphase to +31ΔGphase over the course of 64 excitations. There is a 250 ms period between
excitations in experiments, which is much longer than the average
time period for a single bubble to pass through the bed (∼60
ms). Therefore, adjacent data samples of MR signal occur at random
relative to the bubble motion in the fluidized bed. Since the samples
occur at random, relative to bubble motion, even with methodical sampling,
the final average will be representative of the average motion in
the bed. In contrast, for the MR-type postprocessing of DEM-CFD predictions,
each simulated pulse sequence was started every 10 ms in order to
shorten total simulation time necessary. Since the simulated pulse
sequences occurred at a higher frequency than bubble passage through
the fluidized bed in the simulations, methodical sampling would have
caused adjacent lines in k-space to be linked to
the same particle velocity associated with nearby points in bubble
motion, corrupting the ultimate time-average. For this reason, the
phase-encoding gradients were changed randomly from −32ΔGphase to +31ΔGphase to mimic the randomness in sampling inherent in experimental MR
imaging. To further mimic time averaging and improve signal-to-noise
ratio (SNR), 32 full signal images in k-space were
summed.In total, four separate simulations with different initial
packings
of particles were used to simulate 5 s of steady bubbling each. The
20 s of steady bubbling fluidization from this ensemble of simulations
was used to attain 32 images in k-space, which were ultimately converted
into one time-averaged velocity image in real space.The slice-selective
pulse and gradient were modeled in the DEM-CFD
postprocessing by weighting the signal of each particle by a Gaussian
function (eq 5), based on the y-position of each particle at the time of the slice-selective pulse,
as shown in Figure 2. The magnitudes and durations
of the gradients were set to match those used experimentally by Holland
et al.[6]After the signal map, Sunweighted,
from all 32 k-space signal images was obtained, it
was weighted to account for T2* relaxation around the time of
the spin echo. Since the spin echoes formed experimentally at the
center of k-space in the x-direction,
this was accounted for in the MR-type DEM-CFD postprocessing by weighting
the final signal map in the k direction according towhere td = 10
μs is the dwell time between points sampled during the simulated
readout. The T2* value was set to 0.6 ms to match that measured
experimentally for the poppy seeds used in the Holland et al.[6] experiment. The signal map was then transformed
into an intensity map in real space via a 2D Fourier transform. The
complex phase, ψ(x, z), of
each pixel in the intensity map, Sweighted(k, k), was then extracted and converted
into an average particle velocity, according towhere vavg,MR-type(x,z) is the MR-type time-averaged
velocity in voxel (x,z), Δ
= 2 ms is the duration between the two flow encoding gradients, δ
= 0.56 ms is the length of the flow encoding gradients and Gflow,max is the magnitude of the flow encoding
gradients. The final velocity map was produced by taking a regression
for each pixel among three different phase maps produced using Gflow,max −0.045, 0, and +0.045 T/m to
ensure that the velocity map was not skewed by minor velocity encoding
arising from the imaging gradients.
Results
The experimental results for time-averaged particle velocity were
first compared with the DEM-CFD results averaged using the MR protocol,
to validate the model. The DEM-CFD results were then analyzed using
the other averaging techniques to examine if MR-type averaging matched
a particle-based average and how far this averaging deviated from
other averaging techniques.Figure 4 gives
a comparison of the time-averaged
velocities of particles in the axial direction. It compares the MR-type
averaging procedure of the DEM-CFD results with the experimental MR
imaging results from Holland et al.[6] The
two velocity maps show a similar profile of upward particle velocity
in the center of the bed and downward particle velocity along the
sides. This result matches the expected “gulf-stream”
profile seen in small fluidized beds in which single bubbles rise
predominantly through the center of the bed. Particles are rapidly
carried up with the bubbles through the center and then slowly return
to the bottom of the bed, moving down near the walls. The difference
map (Figure 4c) shows little difference between
the DEM-CFD and the MR imaging results in the bulk of the bed, with
the greatest difference in magnitude occurring at the top of the expanded
bed. The DEM-CFD simulation underestimates the velocity measured by
MR at the central region at the top of the bed, while it overestimates
the MR velocity in the outer regions at the top of the bed.
Figure 4
Comparison
of average axial velocity images from (a) experimental
MR imaging[6] and (b) MR-type postprocessing
of the DEM simulation. Image (c) gives the difference map between
images a and b. The field of view for each image is 47 mm (z) by 44 mm (x) and the resolution is 1.04
mm (z) by 0.94 mm (x).
Comparison
of average axial velocity images from (a) experimental
MR imaging[6] and (b) MR-type postprocessing
of the DEM simulation. Image (c) gives the difference map between
images a and b. The field of view for each image is 47 mm (z) by 44 mm (x) and the resolution is 1.04
mm (z) by 0.94 mm (x).Figure 5 shows a comparison
of the time-averaged
velocities from the results of the DEM-CFD simulation using different
time-averaging techniques. In all cases, the magnitude of the upward
velocity exceeds the magnitude of the downward velocity. The velocity
maps in Figure 5 panels b–d show little
difference among the various weighting procedures used for particle-based
averaging. Additionally, these particle-based averages yield a very
similar velocity map to that of MR-type sampling, processing, and
averaging, shown in Figure 4b. Figures 5e and 5f show that frame-based
averaging using the “frame 1” and “frame 2”
methods heighten and dampen the magnitude of the time-averaged particle
velocities, respectively, compared with particle-based averaging.
Figure 5
Comparison
of average axial velocity images of DEM simulation with
different averaging methods: (a) MR-type postprocessing, (b) volume-weighted,
Gaussian-slice particle-based average, (c) Gaussian-slice particle-based
average, (d) “top-hat” slice, particle-based average,
(e) “frame 1” frame-based average, and (f) “frame
2” frame-based average. The field of view for each image is
47 mm (z) by 44 mm (x) and the resolution
is 1.04 mm (z) by 0.94 mm (x).
Comparison
of average axial velocity images of DEM simulation with
different averaging methods: (a) MR-type postprocessing, (b) volume-weighted,
Gaussian-slice particle-based average, (c) Gaussian-slice particle-based
average, (d) “top-hat” slice, particle-based average,
(e) “frame 1” frame-based average, and (f) “frame
2” frame-based average. The field of view for each image is
47 mm (z) by 44 mm (x) and the resolution
is 1.04 mm (z) by 0.94 mm (x).The analysis of Figures 4 and 5 shows that the magnitude
of the time-averaged profile of
velocity measured by experimental MR imaging is best matched by that
of the MR-type analysis and particle-based averaging of DEM-CFD results.
The maximum upward, and downward, time-averaged speeds measured by
MR are still greater than those yielded by MR-type processing of DEM-CFD
results. Additionally, the profile of upward velocities determined
by experimental MR measurements, occurring around the axis of the
bed, extends to a higher vertical position than that yielded by the
MR-type processing of DEM predictions, suggesting that the DEM-CFD
bed has expanded slightly less than the experimental bed.Figure 6 shows the time-averaged axial particle
velocity for the different averaging procedures for a vertical slice
on the axis of the bed (top), a horizontal slice 20 mm above the distributor
(middle), and a horizontal slice 35 mm above the distributor (bottom).
These results are consistent with those shown in the velocity map,
in that MR-type postprocessing and particle-based averaging have very
similar velocities which are closest to the experimental MR imaging
data, while “frame 1” averaging gives significantly
higher, and “frame 2” averaging gives significantly
lower, velocities.
Figure 6
Comparison of average axial velocity (m/s) images with
different
time-averaging methods along (a) a vertical slice at the x-direction centerline, (b) a horizontal slice 20 mm above the distributor,
and (c) a horizontal slice 35 mm above the distributor. The different
averaging methods compared are (i) MR-type postprocessing (◇),
(ii) “top-hat” slice, particle-based averaging (□),
(iii) “frame 1” frame-based averaging (○) and
(iv) “frame 2” frame-based averaging (△). The
averaging methods are shown in comparison to the experimental MR imaging
results[6] (●).
Comparison of average axial velocity (m/s) images with
different
time-averaging methods along (a) a vertical slice at the x-direction centerline, (b) a horizontal slice 20 mm above the distributor,
and (c) a horizontal slice 35 mm above the distributor. The different
averaging methods compared are (i) MR-type postprocessing (◇),
(ii) “top-hat” slice, particle-based averaging (□),
(iii) “frame 1” frame-based averaging (○) and
(iv) “frame 2” frame-based averaging (△). The
averaging methods are shown in comparison to the experimental MR imaging
results[6] (●).Table 5 shows the spatially averaged
sum
of squares of the deviation of axial velocity for each averaging technique
as compared to the MR-type postprocessing and the experimental MR
imaging results according to the equationswhere Δvavg,MR–type2 and Δvavg,MR2 are the square of the deviation from MR-type average and experimental
MR imaging results, respectively, of a particular averaging procedure,
taken over a spatial domain consisting of Npixels. The velocity vavg(n) is the time-averaged axial velocity from that averaging procedure
at voxel n. Also, vavg,MRI-type(n) and vavg,MRI(n) are the time-averaged velocity from the MR-type averaging
of DEM-CFD results and the actual experimental MR imaging results,
respectively. The domain of Npixels consisted
of all pixels up to 40 mm above the distributor. Pixels above this
height were not used because the bed in the simulation did not expand
much beyond this height and if these pixels had been used, the deviations
would have been dominated by this region of the bed. Additionally,
the experimental results could be inaccurate near the top of the field
of view because particles in this region can go undetected if particles
enter or leave the radio frequency (rf) coil between the initial rf
pulse and signal detection. Table 5 shows that
the particle-averaging procedures produce very similar time-averages
to the MR-type processing, while the frame-based techniques deviate
significantly. MR-type processing matches the experimental MR imaging
results the best, and particle-based averaging procedures also match
the MR results well, while frame-based averaging procedures deviate
significantly.
Table 5
Comparison of Time-Averaged Velocity
Results for Experimental MR and DEM-CFD with Different Averaging Proceduresa
averaging procedure
squared velocity difference from MR-type post-processing (m2/s2)
squared velocity difference from experimental
MR5 (m2/s2)
frame 1
45.9 × 10–3
34 × 10–3
frame 2
5.10 × 10–3
17 × 10–3
particle-based, top-hat slice
0.318 × 10–3
5.8 × 10–3
particle-based, Gaussian slice
0.316 × 10–3
5.8 × 10–3
particle-volume-based, Gaussian slice
0.314 × 10–3
5.7 × 10–3
MR-type postprocessing
0
5.1 × 10–3
The squared difference in time-averaged
axial velocity spatially averaged over the voxels of encompassing
the fluidized bed is given by [Δvavg2 = 1/Npixels ∑Npixels(vavg(n) – vavg,MR(n))2].
The squared difference in time-averaged
axial velocity spatially averaged over the voxels of encompassing
the fluidized bed is given by [Δvavg2 = 1/Npixels ∑Npixels(vavg(n) – vavg,MR(n))2].
Discussion
Comparison of DEM-CFD Results
with Experimental
MR Results
The overall profile and magnitudes of upward and
downward velocity for the experimental MR measurements (Figure 4a) and the MR-type postprocessing of DEM-CFD results
(Figure 4b) are in good agreement, cross-validating
the DEM-CFD model and the MR measurements. The slightly higher maximum
upward and downward speeds as well as the larger maximum upward velocities
seen in the MR measurements, as compared to the DEM-CFD results, can
probably be attributed to either (1) inaccuracies in modeling the
contact mechanics or (2) inaccuracies in modeling the drag force.
Inaccuracies in modeling contact mechanics could arise from the fact
that the spherical particles used in the model would contact each
other differently to nonspherical seeds used in the experiment; however,
it is not apparent why this discrepancy would cause the differences
noticed in the results. Additionally, inaccuracies in modeling the
contact mechanics could stem from the values of the contact parameters
used in the DEM-CFD simulation. However, this seems unlikely since
Müller et al.[13] have already found
the effect of varying these parameters over wide ranges to be insignificant.The case for the difference in results being attributed to problems
in modeling drag is much stronger. Using spherical particles to model
nonspherical seeds affects the degree of drag, because nonspherical
particles have a higher ratio of surface area to volume, which could
lead to higher drag and a larger bed expansion. Additionally, the
drag law of Beetstra et al.,[27] used here
and developed for modeling fluid-particle interaction with spherical
particles in fluidized beds, has been demonstrated to underestimate
drag by Kriebitszch et al.[34] The latter
found that in a direct numerical simulation (DNS) of a fluidized bed,
the drag force which would be calculated on particles using the drag
law of Beetstra et al.[27] in a DEM-CFD simulation
was on average 33% lower than that determined by the DNS simulation
using the no-slip boundary condition. This lower average drag would
account for the lower time-averaged upward axial velocity in the DEM-CFD
simulation as compared to the MR experiment. A separate study[35] comparing DEM-CFD to DNS simulations suggested
that the drag law in DEM-CFD simulations is most inaccurate around
the sides of bubbles, since particles are not evenly distributed in
fluid cells and particles can move in vastly different direction and
at different velocities from one another. This suggestion can account
for the fact that the predicted time-averaged velocity profile is
very similar at the sides and the bottom of the bed, yet less accurate
in the upper, central portion of the bed, where the largest bubbles
pass through the system. Additionally, Kriebitszch et al.[34] found that the bed expansion in a fluidized
bed modeled using DEM with the drag law of Beetstra et al.[27] was lower than that in a fluidized bed modeled
using DNS. This observation is consistent with there being less bed
expansion with the DEM-CFD results (Figure 4b) compared with the MR results (Figure 4a).Some steps could be taken to improve the modeling of drag force
in this DEM-CFD system. (1) Simulated particles could be made nonspherical,
matching the shape of the poppy seeds used experimentally, and a drag
law similar to that of Beetstra et al.[27] developed for nonspherical particles can be used. (2) A drag law
could be developed to account for particles moving in different directions
and at different velocities relative to their neighbors. (3) A filter
for a drag law could be created and implemented to calculate drag
in fluid cells which have uneven distributions of particles because
they lie on the outskirts of a bubble.
Comparison
of MR-Type Postprocessing with
Other Averaging Procedures
The similarity between the profiles
and magnitudes of the time-averaged particle velocities yielded by
MR-type postprocessing of the DEM-CFD data (Figure 5a) and particle-based averaging (Figures 5b–d) demonstrates that MR imaging effectively yields
a particle-based time-average of axial velocity. This similarity is
expected because the magnitude of the MR signal is weighted by nuclear
spin density, which is proportional to the volume of particles containing
the nuclear spins. This similarity also demonstrates that the sampling
and other aspects of MR imaging mentioned in section 4.3, which could
lead to artifacts and imperfections in MR measurements, do not cause
MR time-averages to deviate significantly from particle-based averages.
Additionally, the similarity between Figure 5 panel b and panel c shows that, for fluidized systems with a small
variance in volume of particles (e.g., σ/Vavg < 0.06), weighting an
average by the number of particles rather than volume of particles
has little consequence on a time-averaged velocity. The similarity
between panels c and d in Figure 5 shows that
weighting based on a Gaussian slice versus a top-hat slice also does
not greatly affect time-averaged velocity. Further investigation showed
that the time-averaged velocity results were insensitive to slice
thickness when both Gaussian and top-hat slices were taken with thicknesses
from 2 to 10 mm, indicating that particles in this range of slice
thicknesses possess the same time-averaged flow field.The vast
difference in the magnitudes of the time-averaged velocity maps of
the frame-based averaging (Figures 5e,f) and
the MR-type postprocessing (Figure 5a) demonstrates
that MR imaging could yield different time-averaged properties of
dynamic systems than other experimental procedures, such as PIV. The
increased magnitudes of upward and downward velocities in Figure 5e shows that particles tend to move at greater speeds
when they do not have other particles in their immediate vicinity
and an experimental procedure which sampled and processed data in
a similar fashion to “frame 1” averaging would capture
this effect. The lower magnitudes of upward and downward velocities
in Figure 5f show that an experiment which
interpreted a voxel with no signal from particles at a particular
instant as having zero velocity would significantly reduce the magnitude
of the time-averaged velocity compared with that obtained from MR
imaging. In any case, these results emphasize that care must be taken
when time-averaged experimental and numerical approaches are compared.
Comparison of Computational Time and Space
Required for Different Averaging Techniques
Figures 5 and 6 demonstrate that a
Fourier-based MR-type time-average of velocity is equivalent to a
top-hat slice particle-based average. Given this conclusion, it is
important to understand the computational time and space necessary
for each of these averaging techniques. While the simulation time
necessary for both techniques is identical, conducting an MR-type
average required approximately 500 GB of data, since particle positions
needed to be output every 10 μs. In contrast, conducting a simple
particle-based average would only require approximately 3 GB since
particle positions and velocities only need to be output every 10
ms. Additionally, with our computer, the postprocessing of the data
for the MR-type average took approximately 1 day, while the postprocessing
for the particle-based average took approximately 1 min. Thus, the
time and space requirements of the two averaging techniques are several
orders of magnitude different, demonstrating that it is desirable
to use a simpler averaging technique when the simpler technique is
equivalent to that used experimentally.
Conclusions
The 3D cylindrical discrete element model developed and used in
this study was validated by the similarity in axial velocity profiles
and magnitudes between an MR-type analysis of the DEM-CFD results
and experimental MR results. The slight differences in velocity profiles
and magnitudes appear to arise from problems in modeling the drag
force, both in using spherical particles to model the drag on the
nonspherical seeds and also in using the drag model of Beetstra et
al.,[27] which Kriebitszch et al.[34] suggest might underpredict drag forces. These
drag-related issues are deserving of further work.When comparing
DEM-CFD and experimental results, it is very important
to have the postprocessing procedure of DEM-CFD match that of the
experiment as closely as possible. Experimental MR sampling, processing,
and time-averaging of data from dynamic systems corresponds closely
to a particle-based time-average and is very different from a frame-based
time-average. Here, the postprocessing procedure on the raw DEM-CFD
data made a much larger difference on the ultimate results than the
difference seen in studies varying DEM-CFD parameters, such as drag
law.[13,27]The numerical simulations were also
used to test the effect of
the excitation profile used in MR imaging. Simulations were analyzed
using both Gaussian and top-hat slices with thicknesses of between
2 and 10 mm. Time-averaged velocity profiles for all of these simulated
slice excitations were essentially identical. These results indicate
that particles in this range of thicknesses have the same time-averaged
flow field, and validate the use of Gaussian excitation profiles in
MR.
Authors: Tyler R Brosten; Sarah J Vogt; Joseph D Seymour; Sarah L Codd; Robert S Maier Journal: Phys Rev E Stat Nonlin Soft Matter Phys Date: 2012-04-05
Authors: C R Müller; J F Davidson; J S Dennis; P S Fennell; L F Gladden; A N Hayhurst; M D Mantle; A C Rees; A J Sederman Journal: Phys Rev Lett Date: 2006-04-21 Impact factor: 9.161
Authors: C R Müller; D J Holland; J F Davidson; J S Dennis; L F Gladden; A N Hayhurst; M D Mantle; A J Sederman Journal: Phys Rev E Stat Nonlin Soft Matter Phys Date: 2007-02-09
Authors: D J Holland; C R Müller; J F Davidson; J S Dennis; L F Gladden; A N Hayhurst; M D Mantle; A J Sederman Journal: J Magn Reson Date: 2007-04-30 Impact factor: 2.229