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3, 1978
237
Based on process transient response, a procedure for approximating process dynamics by a second-order-dead
time model is developed. The method is general enough to be applied for under, over, and critically damped systems with and without dead time. It also circumvents some of the practical difficulties of the earlier methods.
Whenever information on process dynamics is inadequate, simplified parameters defining a process are usually
determined experimentally. A survey of frequently used experimental techniques, based on deterministic and stochastic
signals, for identification of chemical, metallurgical, and allied
processes is given by Gustavsson (1973). These methods are
of varying complexity, the simplest one being the reaction
curve method involving step response data. This is adequate
for many chemical processes with low to moderate noise level
and has the distinct advantage of involving far less theory and
computations for a practical man to worry about. On the other
hand, processes requiring on-line control techniques, or those
corrupted by high degree of noise, or certain complex systems
(e.g., neuromuscular parameter variations in a pilot during
tracking (Wells, 1972)) may demand elaborate and sophisticated identification procedures. A discussion on this aspect
of the problem may be found in a comprehensive article by
Isermann et al. (1974). Thus the choice of an identification
procedure for a given process would depend upon the objectives of the test, data properties, and available tools and
equipment. However, for chemical processes, it has been
recognized (Latour et al., 1967) that the dynamics may in
general be simplified by an overdamped second-order approximation of the form
e-Ls
G(s) =
(7'1s
+ l)(Tzs+ 1)
G(s) =
(-y
+
2t($)
(5
< 1)
(1b)
+1
0019-7882/78/1117-0237$01.00/0
238
Ind. Eng. Chem. Process Des. Dev., Vol. 17, No. 3, 1978
I
1.0
A-
ml =
Am (1
(12)
X = Xe-x
c(t))dt
(2)
ml = L
+ T I + T2
(4)
where
- ml)Mi
(124
x = In D / ( D - 1)
(12b)
X = (t,
and
(6)
where
D = T1/T2
(7)
0 = TiT2/(Ti - 7'2)
(8)
and
and
and
n
and is provided by a tangent passing through ti and intersecting the final value of c(t) at time t , (see Figure 1).The
value of this time is given by
t, = L
+ 0[ln 17 + ( 0 2 - 1)/7]
(10)
L=ml-4Mie
Oscillatory systems. For X greater than e-l, underdamped
system results for which the treatment follows. In Figure 3 a
typical response curve corresponding to an oscillatory system
is given. Such a curve has at least two points of inflection-one
during rise and another after overshoot. The first inflection
point may be considered analogous to t i for the nonoscillatory
case. Then, starting with the time domain solution of eq Ib,
i.e.
Ind. Eng. Chem. Process Des. Dev., Vol. 17, No. 3, 1978
239
v
c
n
UI
-a
0
._
c
lime, t
( t - L ) ) + cos(-
w,(t
-L))
11
(15)
cos-1 (
- m1)Mi = -
-(
cos-'(
di=-p
( t , - rnl)
w, = -
cor1E )
'/
(16)
and
L = m 1 - - 2E
(17b)
On
I t may be noted that, in order to evaluate rnl used in the preceding three equations, the shaded area in Figure 3 is measured as follows: whenever the area is below the ordinate of
1 it is taken as positive, otherwise negative.
Equation 16 provides an infinity of roots for E for a given
value of A. However, in the region of our interest (0 6 E 6 l),
h is a monotonic function of E, decreasing from a/2 at = 0 to
e-l at ( = 1. Figure 4,which is a plot of eq 16, aids in determining the value of ( for a given oscillatory response. The
other system parameters, wn and L , are then computed from
eq 17a and b. In eq 17a, for c0s-l (, which is a multiple valued
function, its value in the primary period, i.e., in the range 0 to
~ 1 2should
,
be used.
It is important to realize here that, unlike the previous
methods, a knowledge of the point of inflection is not essential
to carry out the preceding parameter evaluation. This is of
practical significance because, for a typical response curve,
it is extremely difficult to locate ti accurately. It may be recalled here that at the point of inflection the second derivative
of the response function vanishes and hence the first derivative is a t its extremum value. When the function, like c ( t ) in
this case, is smooth, the second derivative in the vicinity of ti
becomes small and the first derivative lies near its extremum
value for a considerable period of time (see, for example, AB
in Figure 1).Therefore, location of the point of inflection becomes a sensitive process and for the same reason estimation
of the slope becomes easier. In fact, the greater the difficulty
in locating the point of inflection, the easier it is to estimate
the slope. Hence the present method, in contrast to the previous ones, makes use of the maximum value of the slope
which is easy to determine rather than the time of its occurrence which is difficult to locate. Now the method will be extended to systems with inherent pure delay.
System with Pure Delay. In the equations developed
above, L represents apparent dead time, i.e., dead time due
to the cumulative effect of minor process and measurement
/
/
Tome. min
rn
ml
+ d ; t,'=
t,
+ d ; M I ' = M1
(18)
Illustrative Examples
Example 1. As a first example, let us approximate a
third-order system with time constants of 0.5, 1.0, and 2.0
minutes by an overdamped second-order-dead time model.
The true response curve is shown in Figure 5. In order to apply
the proposed procedure, first the area enclosed by this curve
and the projection of its final value is measured as m l = 3.5
min. Then a tangent passing through the straight line portion
of the response is drawn to yield Mi = 0.23 min-l and t , =
5.10 min. For the corresponding numerical value of ( t , - rnl)
Mi, from Figure 2 , is~read as 0.90. Substitution of these values
T2 and L which agree well with
in eq 13a, b, and c yield T1,
240
Ind. Eng. Chem. Process Des. Dev., Vol. 17, No. 3, 1978
Method
Least square
Present
Meyer et al. (1967)
T1,
min
0.315
0.33
0.32
Primary
Process
T2,
min
1.49
1.50
1.69
1.67
1.54
1.54
1.1
Average
i
0.72
0.85
0.77
0.74
0.77
wn
1.13
1.23
1.20
1.19
1.188
those obtained by a least square curve fit (see Table I). The
present approximation is represented in Figure 5 from which
it is seen that it coincides with the true response almost over
its entire range, thus demonstrating the efficiency of the
suggested technique. The approximation predicted by Meyer
et al. (1967), corresponding to the values given in Table I, is
also reproduced and compared in the same figure. It is evident
that this approximation shows a consistent deviation from
reality which again reflects upon the superiority of the present
method. It is also interesting to note that the earlier methods
due to Oldenbourg and Sartorius (1948) and Sten (1970) altogether fail in this case. To apply these methods, first a ratio
T,/Ty should be obtained from the response curve by reading
the time intervals T, and T y as indicated in Figure 1. This
ratio, for this example, is found to be 0.712, whereas no solution is possible when T,/Ty is less than 0.735.
Example 2. Let us consider, as a second example, a typical
cascade configuration for the inner loop as shown in Figure
6. This represents an oscillatory system. The two blocks within
the loop denote a P I controller with a reset time of 0.5 min and
a secondary process with a time constant of 2.0 min. The primary process is assumed to have a dead time of 0.5 min and
a time constant of 1.0 min. For this case, the response c ( t )to
a unit step change in R is given by
c ( t ) = ~ (- t0.5) [I - e-(t-0.5) - e - ( t - 0 . 5 ) / 2
X {cos((t- 0.5) ~
TO
PlimOry
COntrOller
!i
0.7c
__-
:,:I/i
TrYC
response
Appro.imoI~on
1 Present1
Approximation
Meyer et
01
:::I
,19571
01
Time. mrns
(0.5s
+ l)(s + 1)(2s + 1)
(20)
Ind. Eng. Chem. Process Des. Dev., Vol. 17, No. 3, 1978
241
1.0
Mi
7 5
a
d
p9
54-
3-
.1
'
TIME.
'
'
10
'
12
'
I
14
lo
MINS
Literature Cited