On Design Margin For Process System With Parameter Uncertainty
On Design Margin For Process System With Parameter Uncertainty
P (N, m) = fraction of particles experiencing mixing m Qv = inclination angle of sectionalizing plate [°J
times through N cells pb = bulk density of particles [g/cc]
5 = cross-sectional area of sampling case a2 = variance of residence time of particles
t = discharge time within pneu-escalator [-]
t = average residence time of particles within <f> = dimensionless time defined by Eq.(lO) [-]
pneu-escalator
tc = average residence time of particles within
one cell Literature Cited
6 = dimensionless time denned by Eq.(5) 1) Shinohara, K. and T. Tanaka: J. Chem. Eng. Japan, 5, 279
Of = inclination angle of the filter of (1972)
z=c dx=-i
where C is /-dim. constant vector. Nominal optimum xd
design means that decision variables u and M are where dfjdx represents nXn nonsingular matrix and
determined so that the value of a performance index 9/i/3tt,
dfxldM,
rices, dfJdP represent
respectively. nXr, nXm,
Superscript nXp mat-
- 1 indicates the inverse
/given by Eq.(4) takes the minimum value under the matrix. These matrices are evaluated at P, u, M. Sub-
conditions of given parameter value P and output stituting Eq.(5) into the equation for small perturba-
value C.
tion of Eq.(2), the deviation of output vector z/Z is
given
by the equation
J=g{x, u, M)
+|du dx\Bx) 3aj K' Table 1 Given parameter values and boundary
conditions
where dg/dx, dg/dM and dg/du are n-dixn., m-dim. and
r-dim. row vectors evaluated at u, M and P. In Eq.(8)
mol//,
the coefficients multiplied to AM and Au are not in kB=OA= hr-i,
F^0 100 mol/hr,
C1 =70 mol/hr,
do=0.1 hr-i,
kx=0.02
C2=0.005mol//,
$6=0.01 &//,
general equal to zero. Eq.(7) subjected to Eq.(8) is
reduced to a linear programming (L.P.) problem be- Table 2 Nominal optimum design
cause 0 is a linear function of AM and Au. Hereafter, a Fi=320, 7= 1.27 x01*, S=0.921, /3=0.278
solution of the L.P. problem is assumed to exist. After ^=0.179, xb=0.552, *x=0.020, *F=0.030
iciz=0.219, J=154$
ll, a reasonable design margin AMmay be determined
from the solution of the L.P. problem given by Eqs.
(6)-(8). The design margin obtained by this method partially recycled at the ratio of a to the amount of
(denoted by Method I) may be more rational than that A and B in the inlet flow to the separator, and Xand Y
by the method proposed previously by the authors4'5) are also recycled at the ratio ofp. Denoting the frac-
(denoted by Method II) because the manipulating tion of molar concentration Q [gm°ty^] of each compo-
a
variables admissible in a certain specified range are nentito CA0 (Q=C^5 i=A, B, R, X, Y) by xi9 the
considered. In fact, if the deviation Au ofa manipulat- hourly molar flow rate of fresh feed by FA0 [mol/hr],
ing variable is sufficient to compensate for the undesira- the flow rate of the inlet flow into the reactor which
ble parameter uncertainties and also minimizes 0, the consists offresh feed and recycle flow by Ft [mol/hr]
addition of a design margin to the nominal design ( (volumetric flow rate) X CA:o=Fi), and the volume of
variable is not always necessary. Moreover, it is also the reactor by V, the process equations for steady state
shown from this consideration which manipulating are given by
variable has a strong effect on the values of output FAa+aFiXA-FiXA- V{kB+kx)CA0 xA=0
variable and performance index.
aFiXB-FiXB+ VCAa {kBXA- {kR+kY)XB} =0
Application to Design of a Simple Chemical pFtxz-FiXx + VCA0kxxA=0
Reaction Process with Recycle
PFtXy-FiXy + VC^ kyX^O , (9)
Nominal optimum design at steady state -FixB+ VCMkBxB=0
Let us consider the design margin of the reactor
XA+Xb+Xr+Xx+Xy=1
in a simple chemical process with recycle shown in
Fig. 1 as an example of the method proposed in this where kt (i=B, R, X, Y) [1/hr] shows the reaction rate
paper. The reactor is assumed to be a single C.S.T.R. constant for each elementary reaction. These equa-
with perfect mixing and the type of reaction is assumed tions correspond to Eq.(l) for general expression.
to be Denbigh's reaction, which comprises first order Output state Zx and Z2 are defined as
elementary reactions as shown in Fig. 2. R is the desired Z1 =FixB
product, and this is produced from fresh feed contain- Za= (xX+Xy)CM (10)
ing only A (molar concentration CAo [gmol//]). The
effluent flow from the reactor containing A, B, R, X Zx is the amount ofR produced hourly and Z2 is the
and Y is assumed to be separated into a product flow molar concentration of undesired products X and Y.
containing only R and another flow containing A, B, t is assumed that the values ofZx and Z2 are desirable
Zand 7. Zand Fare undesired products. A and B are to be maintained as
I
VOL 6 NO. 5 1973 455
Table 3 Rational design margin for parameter uncertainty
Design margin
Allowable ranges of AZ±, AZ% --s :
by the method proposed here by the p
case £t $2 £3 AV * Aa Ap AJ AV w
Z2=C2 (15)
Eqs.(lO) and (ll) correspond to Eqs.(2) and (3), The design margin AV can be determined by solving
respectively. For simplicity the following objective he L.P. problem, which is composed of Eqs.(6)-(8)
function is assumed for the numerical calculation. and Eqs.(13)-(15). The result is shown in Table 3
t
j__/volume ofVunit cost \ , f/recycle rate\ for various allowable ranges of AZ± and AZ2. The
J \reactor /\ofreactor/ ' (\ofAandB) design marging calculated by the method presented
_j_/recycle rateN) /unit cost \ in the literature4) (Method II) which does not take
^VofXand Y ))Ifor recycle/
account of operation of manipulating variables, are
" =V$b+ {aFi(xA+xB)+^Fi(xx+xY)} $r (12) also shown in the right column of Table 3, In the case
Practical performance index Jmight be more complex, by Method II, design margin AV cannot compensate
but the above simplification may be enough to illust- for undesirable deviation AZ2 because the coefficient
trate a numerical example of design margin problem. multiplied to AVin the equation of AZ2 is positive and
This form ofJis referred to in the literature1). AZ2 is greater than <J2 even ifAVis equal to zero. That
Nominal optimum design is to determine the values is, by Method II, there is no feasible solution of the L.
of design variable V and operating variables a and ft P. problem composed of Eqs.(6)-(8) and Eqs.(13)-
which minimize the value of performance index Jgiven (15). Then the design margin AVby Method II is de-
by Eq,(12), subjected to Eqs.(9), (10) and (ll) under termined so as to satisfy only the constraint ofAZ±.
the specified values of FA0, CAo, Cx and C2. The From this calculated result the following points are
values of parameters and the boundary conditions concluded, i) Comparing the method proposed in
used in the numerical calculation are given in Table 1. this paper (Method I) with Method II, the design
The results of numerical calculation are shown in margin z/Fand the increment AJ of performance index
Table 2. The following can be recognized from the Jby Method I are smaller than those by Method II in
results; i) p is not equal to zero. Partial recycle ofX each case except for case 1. For example, in case 2,
and Yis more effective than no recycle ofX and Y be- AVby Method I is 233 /, which corresponds to about
cause the output molar concentration ofX and 7, that 2% of nominal value V. On the other hand, AV by
s, Z25 is specified, ii) The optimum recycle rate is 320 Method II is 565 /, which corresponds to about 4.5%
moles/hr in this example, and the optimum retention f nominal value. AJby Method II is about 350 times
time in the reactor is about 4 hr based on CAo. as much as that by Method I. In case 1, AJby Method
Design margin for parameter uncertainty II is about 3 times that by Method I, in spite of the fact
i
For simplicity, the rate constants kB and kx are that AVby Method II is smaller than that by Method
assumed to involve the maximumestimation error of I. Moreover, the deviation of output Z2 due to uncer-
7]° % for absolute values of the nominal values kB and ainty ofkB, kx cannot be compensated by Method II,
kx, respectively. and the deviation AZ2 is about 3 times f2. These re-
sults suggest that Method I is more reasonable than
\JkB\^kB,
100 MM,ssi*
Method
II. i ) It becomes clear by comparing case 2
and case 3 that manipulating variable /3 can sufficient-
The value ofrj° is.taken as 20 in this example. It is ly compensate for the effect of AkB and Akx so that
assumed that the allowable ranges for deviation of out- AZ2 is smaller than <f2. It also becomes clear by com-
t
o
put variables Zx and Z2 are given by paring case 2 and case 5 that the estimated design
margin AV decreases if fx becomes smaller, iii) If£3 is
4Zi^-£i, f2^jz2^-f3
greater than or equal to 22.5 X 10"4, the design margin
The movable ranges of Aa, Aft (deviation of manipu- AVis zero, as shown in case 3. Thatis, a and /3 can suf-
lating variables a and /3) and AV (margin for design ficiently control JZ2 within the specified allowable
variable V) are constrained by ranges of AZ2.
»l =3.8x lO"3^0-^0-65
Introduction and Analysis
The data obtained are also compared to the analysis
Chun and Seban2) experimentally investigated the of Dukler3) and it is observed that the deviation be-
falling-film evaporator under turbulent flow condi- tween the experimental results and the theoretical
tions of the liquid film. The data obtained are corre- analysis is considerable. Dukler3) obtained heat trans-
lated by the following non-dimensional equation for fer rates in falling films by numerical integration, and
the turbulent flow of the film. the analysis did not offer any straightforward equation
to facilitate ready computation. The present note at-
* Received on April 2, 1973
K. Sarma
tempts to establish an equation for heat transfer coeffi-
Department of Mechanical Engineering, College of Engineering, cient in explicit form making use of some of the availa-
Andhra University, Visakhapatnam-5300 1 3, India ble hydrodynamic aspects of falling liquid films. The
P
VOL. 6 NO. 5 1973 457