by
:Earl Gage
ColeSUBMITTED IN PARTIAL FULFI
L
LMENT OF THE
REQUIREMENTS FOR THE DEGREE OF
BACHELOR
OF SCIENCE
in the
MASSACHUSETTS
INSTITUTE OF TECHNOLOGY
(1951)
S
i
gnature
ofAu
th
o
r
• • • • • "' .... i • • •Signature redacted
-.-• -• • • -. -• • • • • • • • • • • • • • • •• • • • •Depar
t
m
e
nt
ofPhysics
,
May 18, 1951Signature redacted
Certified
by --
.
-
-_______..,
..
' - -~--
----,---
--•
• • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • ••
•Professor Josephs. Newell
Cambridge, Massachusetts
May 18, 1951
secretary of the Faculty
Massachusetts Institute of Technology
Cambridge, Massachusetts
Dear Sir:
This thesis, entitled "Analysis of Aerosol
Co-agulation in a Sound Field", 1s respectfully submitted in
partial fulfillment of the requirements for the Bachelor
of science Degree.
Yours very truly,
Signature redacted
F.arl
G.Cole
EGC :kr
A statistical analysis was made of the coagula-tion phenomenon of an aerosol in a sound field. The effect of changing important variables has been determined.
Quanta-tive calculations have been made and the results give trends that agree with the physical facts; however, the calculations have not been extended to a point where satisfactory com-parison with experimental data can be made.
tude and to extend due credit to Dr. Francois L. Giraud, who holds a Richard C. DuPont Post-Doctoral Memorial
Fellow-ship at the Gas Turbine Laboratory, for his assistance in
the development of the statistical analysis of this thesis.
His earlier work in this field established a general
founda-tion for constructing the analysis. To Professor E. P.
New-man, thesis supervisor, the author is grateful for his many
helpful suggestions and the backing that he provided.
The efforts of Mrs. Antonia Walker and Mrs. Eileen Gillis in making the computations is greatly appreciated.
Finally, the author wishes to thank Mrs. Kitty
Rathbun for typing this thesis.
Letter of Transmittal Abstract . * . . . .* Acknowledgements . . . List of Figures . . . List of Symbols ..*. Introduction . . . . Statistical Analysis Cbmputations. . Discussion of Results 10.
Bibliography
0 . 11. Figures . . . 0 12. Appendices . . . . . . . . . . . . .0 . . . . . . . . . . . . . . . 0 . . . 0 . . . . 0 0 . 0 . . . .* . . . . .0ii
iv vi vii 1 4 1. 2. 3. 4. 5. 6. 7. 8. 9.1. Variables Effecting Collision Efficiency
2. Derivation of Laws of Motion . .* . . . .
V 17 .. .. . . .. . . .21 .. . . . . 24 . ... . . . . . 25-32 33 37
Fig. Title Page
1 Initial Distribution Function . . . . . 25
2 Cyclone Efficiency Curve. . . .
.26
3
0*vs
x 0 0 40 e 0.. ... ...
27
4 Volume of Particle per Volume Interval dx* vs x
Case
2
. .. . . . 285 Volume of Particle per Volume Interval dx* vs x*
Case
1
. . . 296 Rate of Change of Distribution Function . . . 30
7 Collection Efficiency vs Time . . . . . 31
8 Number of Particles Per Unit Volume vs Time . . . 32
A B C co d E f g (x, t) H(xIx2)
J
K
1
Nn(t)
Distribution amplitude Constant (Dimensionless)Dimensionless Parame ter
Velocity of Sound Particle diameter Cyclone efficiency Frequency Distribution function Collision rate Sound intensity
Parameter (Define in text Eq.21)
Mean distance between particles
Collection efficiency
Number of particles/unit volume
- 7 6 M-w
em/sec
cm = 10+4 microns sec 1l cm-6 secm watts/cm2 cm3/sec cm --- a ---w Collision efficiency Radius of particle Particle amplitudeMean particle amplitude Time Particle velocity Gas velocity
vii
Q
r
S
t
u p'119
cm cm cmsec
cm/sec
cm/sec
W Grain loading
x Volume of particle
y Volume of particle (variable of
integration)
Greek Letters
,P Density of paw ticle
J1
Density of gasViscocity of Gas
C(
Dimensionless velocity parametergm/cm3
cm
3 CM3cm3
Superscripts
Dimensionless quantities
Change in variable
Subscripts g pertains to gas p pertains to particle 0 reference variable1 denotes a particular volume
2 denotes a particular volume
viii
gm/cm3
gm/cm3
The object of this thesis is to present an analysis
of the phenomenon of aerosol coagulation in a sound field. An
attempt has been made to develop a theory that will predict the principle variables involved and determine their relationship to the coagulation rate. The main application of the phenomenon is as an intermediate step in the process of industrial
col-lection of aerosols. The large Brownian motion of extremely
small particles (less than one micron in diameter) cawaes these
particles to agglomerate; therefore, sizes less than one
mi-cron are seldom encountered in practice. There are centrifugal
machines which can collect particles larger than ten microns
in diameter with an efficiency of about 90 percent. Sonic
ap-plication is in the range of particle sizes from one to ten
microns where an attempt is made to make small particles grow into larger particles by agglomeration.
The term aerosol is used to define particles that
are dispersed in a gas. The term pertains to both solid and
liquid substances and covers the familiar types which are called
smoke, dust, fume, etc. If the aerosol is a liquid, the
parti-cles will be spheres; small solid partiparti-cles, however, will also behave essentially as a sphere.
-It was observed over fifty years ago that sound waves would cause particles of an aerosol to agglomerate. Numerous experiments were carried out in an attempt to deter-mine the Oause of the coagulation and to deterdeter-mine the forces
acting on the particles. The general conclusions arrived at
from the results of these early experiments are that there
are three main effects.that could cause agglomeration. They
are:
(1) If a distribution of small spherical jarticles
are introduced into a sound field, they will be caused to oscillate with different amplitudes
de-pending upon their size. This relatively
in-creased motion will result in more collisions per
unit time than by normal thermal agitation and
will greatly increase the, agglomeration rate. Ref. (5,7)
(2) A hydrodynamic analysis of the forces between
two spheres which are at rest in a vibrating medium results in both attractive and repulsive
forces which are inversely proportional to the four power of distance between particles.
Ref. (6,3)
(3) The third effect is the phenomenon of acoustical radiation pressure. An ana2ysis of the forces
waves shows that the sphere migrates toward the
node. Particles, therefore, will tend to collect
at nodes and agglomerate. This effect is easily
observed in a sound tube with standing waves using
a stationary aerosol. In the case of a moving
aerosol passing through a sound chamber with
standing waves, it is reasonable to assume that
this effect will only increase the turbulence of the flow and aid in the coagulation process by maintaining a random distribution of the particles in space.
It is the desire of the author to formulate a theory that will aid in the design of more efficient industrial col-w
lectors. In this analysis, a mathematical representation of
the coagulation phenomenon of an aerosol flowing through a
sound chamber with standing waves is formulated. The
stipula-tion of a fldwing aerosol is made since this condition tends to
maintain a more random distribution of the particles in space and supports one of the basic assumptions made in the analysis
STATISTICAL ANALYSIS
The present analysis is based on a simple statis-tical interpretation of the collision phenomenon of small
particles in a moving gas exposed to a sound field. The most
important' assumption which we have to make is that of the laws
of motion which the particles in .the sound field obey. In
this analysis, the assumption is made that the motion of
dif-ferent-sized particles relative to each other is the dominant
one in the range of particle sizes in which we are interested.
We will neglect hydrodynamic forces and the influence of radia-tion pressure, except to the extent that it will produce a
more random distribution of particle position. For these who feel that this may be too strong an assumption, let us point
out that the hydrodynamic forces could be included by consider-ing the effective cross-section of each particle as beconsider-ing
en-larged slightly, since the hydrodynamic forces are proportional
to the reciprocal of the fourth power of the distance between two particles and do not become significant except at small dis-tances.
We, therefore, make the following assumptions:
(1) Particles move with the root mean square value of
the following relation
-where
(up) max (ug)max
41Tfr2
+ 1L4Fg I
(1)
(See Appendix 2)
(2) The particles are essentially spherical
(3) The particles are independent, that is electri.
cal, gravitational, and magnetic forces are neg..
lected.
(4) Collisions result in particles whose volumes
are the sum of the volumes of the colliding par-ticles.
(5) The distribution of particles in space remains random.
We consider a non-homogenous aerosol with particles
of various sizes given by a distribution function.
Let x 3 volume of a particle
g(x,t) : distribution function : number of particle per
unit volume per volume element dx
n(t) : number of particles per unit volume at any time (t)
dn(x,t) * number of particles per unit volume having their
volume between x and x + dx
Therefore dn(x,t)
=
g(x,t) dx.'. dn(x,t) n(t) a g(x,t)dx
0 0
(2)
The invariant in the problem is the total mass or rather the
volume since the density is a constant. Therefore
00
V .fx g (xt) dx =constant. (4) 0
The mechanism of coagulation is a collision
phenome-non; therefore, we must calculate a rate of collision between
the particles of different sizes. We assume that the particles can be considered as having a velocity given by equation (1). Equation (1) represents the velocity amplitude of a sinusoidal varying velocity, therefore we want to use its effective value.
(uP)eff, (Up)max x -V2
Brownian motion of particles, ineffective collisions, and tur-bulence of the flowing gas in the sound chamber will tend to
maintain a random distribution of particles in space.
We define the following quantities:
Q
z collision efficiency - It will probably be a functionof a nuxaber of particles per unit volume (n(t)]j, the maximum and minimum relative velocities, and finally a function
of any given aerosol.
H(x1
,
X2 ) = number of effective collisions per unittime between a particle having volume x with all the particles having volumes
x2 and x + dx
dn(x2 ,t) zg(x2 ,t) dx2 a number of particles per unit
volume having volumes between x2 and X2 +d2 (5)
We assume that the particles of volume x2 are
sta-tionary and let particles of volume x. move with velocity
ul - u2Ieff* Then the effective volume for collision
wiT
(r + r2)2 u - u2Ieff. (6) Therefore H(x1 , x2)Q1T
(r1+ r2)2 u - u2 eff (7) using r=X
(8)
We have H(x,,x2) =L(X1
+ x2 )1 ul-u2 Jeff dh(x2tt) (9)Let us examine more closely the types of phenomena
that the collision efficiency (Q) would have to represent. The
U &
amplitude of a vibrating particle is given by S where
2*w
ot depends on the mass of a particle and variesfrom 1 to zero
and is defined more explicitly later in the text. When the
mean distance between particles (1 T V_ ) increases to a
value larger than the vibrating amplitude of the particle, the
number of collisions per unit time will become small.
There-fore as the number of particles decreases, the collision
ef-ficiency (Q) will decrease as a function of time. If the
As the parameter (S - 1) approaches zero, the collision
ef-ficiency will decrease rapidly. If the intensity and
fre-quency are such that the quantity (S-1) is large at the initial
time (t
=
0), then Q ~%l and will decrease slowly with time (SeeAppendix 1). The collision efficiency could also contain the
influence of a meximum and minimum velocity. There may be a
minimum velocity below which there will be no effective
col-lisions resulting in agglomeration. There may also be a
maxi-mum velocity above which collisions will result in disintegra-. tion instead of agglomeration. The exact nature of this
phe-nomenon is unpredictable.
Finally, the collision efficiency will depend upon the type of aerosol. Attractive forces that hold the particles
together will depend largely upon the physical and chemical properties of the aerosol.
It might seem at first sight that we have included
too many unknowns into a single parameter (Q), but if the
in-tensity, frequency, and grain loading are not too unfavorable, the collision efficiency should remain almost constant over a
time interval of the order of several seconds.
We now proceed to calculate the variation in the
num-ber of particles of volume x in a time St.
Let y = variable of integration
Therefore
X/ X max
Idn(x,t5 rj
H(y,x-y) dn(y,t) - H(x,y) dn(yt)j t (10)min X min
The first integral in equation (10) represents the collisions between particles that tend to increase dn(x,t), while the second integral represents the collisions between particles of volumes x with all of the other particles, thereby leading to a decrease in dn(xt). After combining equations 5, 9, 10, we
pass to the limit, and cancel common terms. Therefore, the
governing equation has the form
In order to generalize the theory and make the equa-w tions more simple for computation, we introduce a dimensionless volume ratio into our equation.
Let
x*=
x0a
and1
*Y
0 X0anywhere x0 will be the vol-.
ume of a particle with some reference diameter do.
rITd
0
(12)
It is also desirable to have the velocity dependence on a
dimen-sionless basis.
Therefore
(up)eff
=
.707 (ug)max
41T f JP 43 II -tl i y.Lx where r x Now, if we let 2 -f2 d94 C 2 7 2
81
(14)
=
-- drrP,.we can write
.707 (u m p eff*(15)
(13)
4hr where XO CC X*/ + 11-0
Since .707 (ug)ma is a constant for any given intensity, we can take it out of the integral sign. For computation purposes,
we then define
o
1/2(16)
IC + 1
The velocity then has form (up)eff .707 (ug)m
oL
Combining these dimensionless terms, we can transform equation
(11) into the following form:
2/3 Ig(xt)
Q
x (.707) (u)M
(X*t)
12 (17) where x* max 2-( x--)g(y*,t)g(x*ey ,t)dy* x min V3*/x ma
and I2
TLx
+
y] OX)-- O((y)I g(y*, t)dy* (19)x* min
By use of the well known relation between velocity
amplitude of particles in a gas and the intensity of the sound field, we can reduce the terms preceeding the bracket in equa-tion (17).
u4W2j(20)
where
j
=
sound intensityfg
=
density of gasCog velocity of sound
Let K represent this collection of terms. After simplifica-tion, we get
Qd2-
Q
d
FK
=(
2 (21)4 C 0
where now we can see the dependence of the important variables.
Equation (14) can now be written in the simple form
g(x*, t) K I'
g(x,t)
12(22)
The general equation is very difficult to solve
since it is a non-linear partial differential integral equation. However with certain assumptions it is possible to solve it
numerically.
we
can consider it essentially as a initial valueproblem where we are given the distribution function g(x*,O) at
time t
=
0* Then we can proceed step by step to the newdis-tribution by using the series expansion, neglecting terms of higher order.
g(x*,t
2)g(x 'tl' +
At21 1 gLj...
(23)will allow us to follow the agglomeration process as a function
of the exposure time in the sound field.
The magnitude of the distribution function is
deter.-mined essentially by the grain loading of aerosol and the
ref-erence volume.
Let
W: grain loading (gm/am3)
then
W
fix
x* g(x*,O)dX* (24)0
For the present calculations, g(x*,O) was assumed to be of the
following form:
g(x*,0) a A x*
e
(25)where x* a 1 was taken to be most probable size. Therefore
since x*M _ X 1 we can pick the reference volume xo to be
the probable particle size in the distribution. The constant
A is determined by equation (24) with a given WfP, x0.
The variation of grain loading will be reflected in
the following manner. Suppose we have the r esults for a given
initial function g(x*,O). Then we change the grain loading
keeping the density and xo constant. That is, g'(z,) - B g(x,O)
where
B;Z
const.
Then g,
(x*,t)
= gt(x*,0)g'(x*,tl) = Bg(x*,0) + At' B2 age,(X*0)]
where
we go(x*,0)
k[I
-I(XO)
--
L
~
(Y0since I, contains g(x *,0) squardd and 12 contain g(x*,O).
Therefore g' (x*,t)
=
Bg(x*,0) if we let AtB.
Thenthe general effect of a change in grain loading is to change the value of the distribution function and the time scale by a constant. If we decrease the grain loading, that is B is less than one, then we increase the time scale and decrease
the distribution function g (x*,t).
The effect of an intensity change can be seen by
con-sidering equation (23) in a slightly different form.
(xt2)x tt)
+tt.Qdo'Il
- g(x*,t1) 12] (26)_,C, 4
If we change the intensity, holding the other variables
con-stant, we can g et the same result by considering that the time
scale is changed by the square root of the intensity ratio.
Let J' z RJ
then
At'
-If we, therefore, increase the intensity, we increase the co-agulation rate and need less time to obtain any desired amount of agglomeration.
The effect of a frequency change is best represented by selecting different values of the parameter C, which is a
manor factor in determining the relative velocity of the
parti-cles. If we try to change the frequency, holding the parameter
C constant, we have to change the particle density, the reference
volume, or the temperature of the gas. These changes would be
reflected in the parameter K and also in the distribution
func-tion through a change in grain loading. If we change the
par-ticle density to compensate for a frequency change, holding C
constant, we get a change in grain loading. The effect of a
change in grain loading has been discussed previously. Changing
the reference diameter to compensate for a frequency change will result in a change in K and the grain loading. Any change in the parameter K can be compensated by a change in time scale for results that have been calculated for a constant K.
Attempts to compensate for frequency change by a tem-perature change in the gas results in a variation in gas
vis-cosity, gas density, and velocity of sound. Neglecting the
change in particle density, these effects produce a change in
the parameter K and can be calculated by a tine scale shift.
Results for different particle densities can be
ob-tained in the following manner. An increase in particle density
and by a grain loading change if we hold the distribution
fune-tion constant. If we want to keep the grain loading constant,
then we must reduce the distribution function and shift the time scale accordingly.
A change in the reference volume is felt in all
para-meters, C, K, W. To obtain the results of a change in d0 with
given values for C, K, W, we can hold C constant by a frequency
variation, let the time scale shift for the K change and let
the magnitude of distribution function change with another time
scale shift to account for holding W constant.
Thus we see that if we have the computations for a
particular case of a given C, K, and initial distribution
func-tion, we can determine the results of changing different vari-.
ables by shifting the time scale or making compensating changes
in other variables. The fact that a few computations will
lead to a large volume of results for different conditions
COMPUTATIONS
Since the general analysis predicted that the
various parameters varied qualitatively in agreement with
physical observations, some calculations were made for com-parison with experimental data. The initial distribution was assumed to have the form of Maxwell's thermal velocity
distri-bution.
*
g(x*,0)
=
Ax* e-bx*If we take x* x 1 to be the most probable particle size, we
get b 1.
Next, we must specify the various parameters and in-dependent variables, letting the time be the in-dependent variable. Calculations were made using the following values.
do 3 microns (10 4cm)
,P particle density:= 1 gm/cm3
Jmax 2 watt/cm2 2 x 107 ergs/cm2
W = 3 grain/ft3 - 6.87 x 10-6 gm/cm3
.-
=
.001205 gm/cm3 T a 200 C, 1 atm.fAg Z181 x 10 6 yAsec T a20 C
Q a collision efficiency a 1 (100f.)
CO0
=
3.452 x 104 cm/sec T=
200 CWith these values the parameter K has value K 5.44 x 10-6
cm3/sec. The coefficient A (the amplitude of distribution
f.P
o
kw
x
*3e
X*
&d
0
where x* max : 3 was taken as the upper limit of integration.
X* a 3 corresponds to a diameter of d
=
3 do z 4.32 microns.Since
fx*Zeix
.261*
X3.xdx*3, we getA
=
9.72 x 105 1/cm3. Therefore,g
(x*,0)
9.72 x 10
5*2 .X
Calculations were made for two values of the parameter C, which is dimensionless.
Case C Frequency with above conditions
1 .0135 669 c.p.s.
2 1.35 6,690 c.p.s.
The initial plan was to extend both calculations to a point where they could be compared with experimental data. After the
calculations were begun, however, they proved to be more
com-plex than was anticipated and there was not sufficient time to
extend the calculations to the desired goal.
The first step in the calculations is to compute the
initial rate of change of the distribution function. Then
several values of g(x*,t1) are plotted with different time
The distribution function must not change too much in any one step or there will be too much distortion in the results. As the calculations proceed, it may be necessary to change the time interval for physical reasons. For example, if the
dis-tribution function should become negative at any time, it
in-dicates that too large a time interval was used.
The distribution function is then computed as a func-tion of time using equafunc-tion (23). The two integrals I, and I2
were computed by using the trapizoidal rule where computation
time dominated accuracy. Even with the approximate procedure,
it was estimated that each integral was accurate to . 3%;
there-fore the distribution functions were accurate to
:
6%.Finally, the results must be put in a form comparable with experimental data. For this purpose, a theoretical
ef-ficiency was defined for a hypothetical collection system. The
system is composed of a sound chamber and a cyclone collector. We assume that the cyclone efficiency curve is that of the
3-inch cyclone efficiency presented in Fig. (2) and that the performance is essentially independent of grain loading.
SOUNO
IM OUT
We define the following collection efficiency.
.z(Mass)in - (Mass)out - (Nass)collected
N -(Mass)in (iass)ln
Since the density is constant, we have
(Volume)collected N a (Volume )in Now x*x z volume of particle at x* and z V* X0
x max
[
x*g(x*,t)dx*,xmin
so that we have N V* collected
V* in x*max
V* collected E(x*) x*g(* ,t) d
x*min
where E(x*) is the cyclone efficiency.
Finally x*max
N
E ()x*g(x*,t)
dx* i*min x g (x *,t) dk* X*MinThe collection efficiency was calculated for each distribution function and is plotted in Fig. 7.
DISCUSSION OF RESULTS
In Figures 4 and 5, the change of the distribution
function with time is presented. The actual parameter plotted
is x* g(x*,t) which represents the amount of the particle
vol-ume per unit volvol-ume between x* and x* + dx** The reason for
plotting tnis parameter is that the area under the curve
re-mains constant and equal to the initial volume V*. To get the
actual volume, multiply V* by x. Since the density is con-stant, these curves also represent the amount of mass at any
particular volume. By computing area ratios, we can
deter-mine what fraction of the total mass is contained in any
vol-ume interval.
The influence of the relative velocity of the
parti-cles,which is expressed by dimensionless parameter c'*, on the
rate of change of the distribution function is demonstrated in
Figure 6. The rate of change curve for case 2 (C = 1.35) is
roughly ten times in magnitude that for Case 1 (C = .0135).
The reason for this difference is easily seen by considering
the oc,* parameter plotted in Figure 3. In case 1, we are
operating on the flat portion of the curve and the relative velocity between particles of different sizes is small;
there-fore the rate of change of the distribution function is small.
large for case 2, it will decrease as the distribution function
moves toward larger volumes. With the present initial
distri-bution function, the agglomeration process would proceed more rapidly with time if a combination of two frequencies were
used. First, use a frequency corresponding to C 1.35 and
then when the mean volume has reached x* * 10, switch to a
frequency corresponding to the C
=
.0135 curve.The result of taking too large a time interval is
demonstrated by considering Figures 5 and 6. If too large a
time interval is taken, the next distribution function will
have too many large particles and a hump will appear in the
distribution function. If we assume this to be physically
correct and calculate the next step using this function, we get the obvious result that the hump will move toward large
volumes. However, these results are distorted in that we are
apt to get too high an collection efficiency and too short a
time scale. Case 1 is an example of selecting too large a time
interval, while case 2 is closer to a continuous process. There
will always be some error becaise of a .finite time interval. Further evidence that case 2 has a more accurate time interval is shown in Figure 8, where the number of particles per unit
volume is plotted as a function of time. These results obey
from a statistical phenomenon of this kind.
Finally, the collection efficiencies presented in
Figure 7 are calculated by multiplying the curves in Figures
4 and 5 by the cyclone efficiency and integrating.
At the present time, these curves have not been ex-tended into the range where they can be compared with experi-mental data. However, they show the correct trends and cal-culations are being continued to extend their application.
BIBLIOGRAPHY
1, Andrade, E. N. deC., "Coagulation of Smoke by Supersonic
Vibrations", Transactions of Faraday Society, 1936,
vol. 322 p.*1111.
2.
... "On the Circulation by the Vibration of Airin a Tube", ProcR Society of London, 1931,
vol. 134, p. 445.
3. Atomic Energy Commission, Handbook on Aerosals, Washington,
D. C., 1950.
4. Bergman, L., Ultrasonics, New York, 1938.
5. Brandt, O., and Hiedemann, "The Aggrigation of Suspended
Particles in Gases by Sonic and Supersonic Waves", Faraday Society Transactions, vol. 322, 1936, p. 1101.
6. Konig, W., Ann. Physik, vol. 42, 1891, p.353.
7. Neuman, E. P., and Norton, J. L., "Application of Sonic
Energy to Commercial Aersol Collection Problems" (Paper to be published soon.)
8. St. Clair, H. W., "Sonic Flocculator as a Fume Settler:
Theory and Practice", . Bureau of Mines, R. I.
3400, 1936, p.51,
9. ta41sir, H. W., Spendlone, M. J., Patter, E. V.,
"Floc-culation of aerosols by intense High Frequency Sound",
o8of Interior, Bureau of Mines, R. I. 4218,
4C
3c
20
tox
FIGURE
I
2..
-3.
E-p-INITIAL DISTRIBUTION
FUNCTION
*2 52
X
5 p--G(X)=9.7,x10
X
e
I I010
_4--- -----C
3
INCH CYCLONE
3MICRONS
6
8
*10
X
IL zw
080
060 zw
U-w
40
20
LL -t k4 # --- IT - t---2
4
12
14
16
18
ititt 4X11111111111111111111 II!IIIIIIIIIIIIIIIIIIII 11 11 I Hwfmn1 rol11
I!
!111!!III ! 1I1I1I1I1I1II II II 1I I MMMII11 1 1 1111 111111I "I 1 1 lw 1'1 1i IIIIIIIII II III
-i!
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INITIAL
DISTRIBUTION
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H
[{KijjJR+t:
---
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FIGUR E
x Hil 1-H1+-H+i- H6
rr V, n-iEl-)
1irl I IT L 42. K3
L 242 46
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W=3.0
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2 (.2
2 -h4HdtH-+H-tA ~HT;T[T4-.4
4' H f#p t-4..6
.8
.o
TIME(SEC.)
FIGURE
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INTENSITY
- ;?J-2
1.4
1.6
1.8
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j
---
--- --- 44-ii VI t ()z H 0
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i i i i i M:
T LEL EEHE I r% IAPPENDIX I
VARIABLES EFFECTING COLLISION EFFICIENCY
The collision efficiency Q may depend upon the
type of aerosol and a possible maximum and minimum velocity
of the particles. The only effect considered here, however,
is the dependence on the relation between the vibrating am.-plitude and the mean distance between particles.
Let
mean distance between particles
0(
-particle
amplitude.2I~4F,
CO
27f
If the particle amplitude is greater than 1, there will be many collisions which will maintain a random distribution of
the particles in space. As the parameter (S-1) approaches
zero, the effective number of collisions is reduced. It may
be possible to handle this effect with a variation in col-lision efficiency.
Consider a specific case. Let us take the following
conditions:
J 2 watt/cn2
g 1.205 x lO- (air T = 200 C) "/ms
c = 3.452 x 104 cm/sec
0(*=
n(o)
=
4.3 x 105 particles/cm3W
=
3 grain/ft
3where n(o) was computed from the distribution function used
in our calculations
fl (o)
J
O(xO)uX'=
4.30
x (0 number/cm30
For this case we have the following table:
Frequency (S) (cm) n(t) (cm) (cps) max. 103 l56 n (o) .0132 5 x 103 .078 n(o)/2 .0167 104 .0156 n(o)/10 .0285 n(o)/100 .0614
If the frequency is low enough, and the intensity is high,
we have (S-1)~10. Under these conditions, we should have
ran-dom motion if n(t) does not decrease too rapidly. In case I,
(f = 669 cps) for which we have made calculations, n(t) has
not dropped to n(o)/2 in one and a half seconds; therefore
our assumption of random motion and a constant Q seem to be
If we had considered a case where n(t) was
chang-ing rapidly so that (S-i) was approaching zero, we would have
had to consider Q changing with time. It is reasonable to
as-sume that Q could be represented by some function (f) which
is functicn of parameter (3-1).
The function f could have the form
f
1 - He I. where H = constant and is practicallyequal to one. 10 is the mean distance at time t =
o.
Then Q would have the form shown in plot below
1.o
For any specific case S and 1 1(t) N would be a
function of time. We would have to calculate a mean
compli-tude S since not all the particles have the same amplicompli-tude and the mean amplitude would decrease with time as the particles grow larger. We can calculate S in the following manners
14
This particular form of
Q
would seem to satisfy all
of the physical conditions in the problem but it would have to
be verified by actual experimental data and an attempt made to
determine the constant H.
APPENDIX II
DERIVATION OF LAW OF MOTION
We assume that a small sphere moving in a gas has a force on it given by Stakets Law
F ".6 1T. rV
where t viscosity of medium
V u relative velocity of particle and medium
r
= PARTICE RAdtuSv has the form (ug - u) where ug is the gas velocity and u is
particle velocity.
tg a u sin wt uo a velocity amplitude
The equations of motion are
m
WE tir
3J
:6
'Y -gr(uo sin wt -u)If we let
z
z9/2
-we get
du
.a (u0 sin wt - u)Solution of this equation is
By using the trigometric identity,
sin ( -3) A sino( cos /S - cosoc sin1
,
we can transform the above equation into the following form:
u n ZUO
z2+w2
sin (wt -)
where
Ntannl
"
z
If we consider only the velocity amplitude, we get
P) max (uma)
+j
1~
4
lyfr2P]12
However, the important quantity is the effective value of the velocity or rather the root mean square velocity.
( (up)eff (up 2
It is a simple integration to show that
pe(uP)Max when the velocity is a sinusoidal