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Abstract. The increased sca rcity of fossil energy resources and the accelerated
worsening of environmental pollution make the pyrolisis of organic materials of
outstanding interest. For this reason, in the Institute of Automation Technology
of University Bremen a laboratory-scale reactor has been installed for pyrolisis
of coal originating from mechanically treated home waste.
In the reactor, the organic mass to be pyrolised is heated both indirectly, via
a set of heat exchan ging tubes, and directly, by recycling the burner exhaust gas.
The reactor is completely equipped by the conventional plant instrumentation and is
directly attached to a process control computer.
The major difficulty in control of the reactor is the simultaneous control of
temperature and pre ss ure at its head, e.g. of two strongly intercoupled process
variables. For this purpose, a multivariable two-input, two-output controller has
been designed, incorporating the mathematical model of the reactor, the parameters
of which have to be repeatedly estimated by the use of actual measured values.
The parameters of the heat balance equations are identified from temperature
profiles in stationary heating state, and the kinetic parameters of the pyrolisis
process via the an alys is of pressure changes under defined temperature programs.
Based on the results of parameter estimation, the control algorithms are used
for gas flow and gas pressure control, taking the interconnection between the
two process variabl es into account, considering the dynamic character of the heat
and material balances of the process. The parameter estimation and control algo-
rithms have been implemented in the process oriented, high-level programming
language PEARL.
It is to be pOinted out that the control problem considered here is at the time
being a crucial one, whose resolving should help to avoid the unsafe reactor
state primarily caused by exothermic steps in the pyrolisis of cellulose containing
biomass.
The preliminary res ults obtained by simulation promise a technically acceptable
solution of the problem and encourage further technical and algorithmic improve-
ments that are carried out in the Institute.
:':1-,
reactor - in order to prevent the penetration of where n is the mole number in the gas phase, V the
the air into the reaction - is completely separa- free space of the reactor, p the reaction pres-
ted from the firing (burning) part of it. This sure, t the time in sec, T the temperature in K,
is achieved by means of a number of heat transfer Q the reactor outflow in mol· see' and R the gas
tubes that indirectly heat the pyrolysis chamber constant In J . mor'. K-'
of the reactor, so that no oxygen penetrates into
this chamber. If Q is zero, the rate of pressure increase cor-
responds to the increase of the number of mole-
On the other side, additional tubes connect the cules in the gas phase by the chemical reaction.
lower and the upper pyrolysis chamber of the Assuming a first order rate eq uati on
reactor and transport the product gas for further dPt/dt = k(~-P\) where k is the rate constant in
processing. sand p the final pressure, and app lyi ng a
linear heating rate, i.e. dT/dt = B, than the
The thermodynamic model derived is based on cor- increase of the pressure with the temperature is
responding heat and mass balance equations. The given by
equations have been written for the following
reactor sUbSYStHl: dp, k
dT = T (p.- p,) (2 )
- surface temperature distribution in the heat where ko is the frequency fa ctor and E the act i-
transfer tubes vation energy in J. mo ~ . The l oga rithmic form
of eq. 2 can be used f or the estimation of the
- axial and a radial heat transfer within the unknown paraneters kO and E from
firing layer of the reactor.
Inr-1_. dp, ] = In ~ _ ~ (4)
In addition to this, a series of basic auxili ary P,-P, dT fl R·T
thermodynamic relations have been used.
This means, that a pre ss ure sensor can be used
The individual equations of the model, as being for the identification of the chemical process.
coupled with each other, are finally integrated
for the simulation purpose, the simulation it- For validation of the pyrol ysis ki neti cs model,
self has been carried out on a large-scale com- developed above, the f oll owing arguments hold.
puter SIEMENS 7880. It requires a software The non-linear increase of PT' star: ing from an
package of approximated 1 MB length that was initial state PI at TI , can now be seen from the
written in FORTRAN 77. Successive simulation
runs have been carried out in (Popovic, Kregel, integrated form of eq. (4 )
1989) in graphic form. For simulation purposes p, T
the following chemical composition of the gas
has been postulated: f~
PI
p-p
F T
= f ~I
T.
fl
. exp ( - ~
R'T
) dT (5 )
resulting in
- exhaustive gas: P,- p,
In - - -
P,- P,
~. ~ [T 2 exp (-~ )
N2 (78 %), H 2 0 (4.64 %), CO 2 (17.36 %) fl E" R'T
CH. (50 %), C. H,o (16 .66 % ) The maximum rate of pre ssure increase will be at
Cs H'2 (16.66 % ), Cl H,. (16.66 % ) the point of 63 % degree of decompos iti on of the
pyrolysis material. This f oll ows from the second
MODEL BUILDING OF THE PYROLYSIS REACTOR derivation of eq. (2)
2
d p _ ko[d(p,-p,) (Ea)
Kinetics of the Pyrolysis dT2 - ~ dT exp - R.T
When deSigning the pressure control of a pyroly-
sis reactor working with a heat-up program, the
non-l i near increase of the pressure by pyrolysis + (p, - p,) :.dT2 ex p ( - : \ ) ] (7)
product molecules in the gas phase, due to the Setting d'p/dT' = 0 in eq . ( 7) and combining it
temperature or the time increase, respectively, with eq . (21, gives at the maximum
should be considered. The increase of product
molecules ifself corresponds to the exponential
increase of the reaction rate with the tempera- (8)
ture.
The overall gas phase mass bal ance for the reac- This, inserted into eq. (6) , gives at the maximum
tor, in which the pressure changes, due to the In p, - p, n w: = - - ; - exp (~ )
decomposition of 3 solid material and the in- PF-P, T III <1 X R·Tm ,1X
crease of product gas phase molecules, are in-
cluded, can be given by
[T~, ,,~ exp(R~; )-TI2exp(:~TJ] (9)
r n.l :,,\ I
dn V dp dp or
(1)
Tt R' T dt - Q dt
In p, - p,-; , ( 10)
- 1
p, - P,
The fraction of non-pyrolized material at the of pressure subsystem, as well as the correspond-
maximum is therefore ing transfer-functions SP' Mp and Rp for its
actuator, sensor and controller. Furthermore, in
P. - PT"""
P. - P,
" ---L
e
2 37 %
I U)
the lower part at Fig. 2, the flow-part of the
model is shown, containing the transfer-function
This result confirms the assumption of first or-
der pyrolysis ki netics, made above. (16 )
Simplified Model for Pressure-Flow-Control of the of the flow subsystem as well as the corresponding
p*rolysls Process transfer-functions Sq ,M q and Rq for its actuator ,
T e hymcdynamics of the coal pyrolysis reactor sensor and controller (Koch, Wendland, 1988).
will for control purposes be described by the
first order nonlinear di ff erential equation
PARAMETER ESTIMATION AND OPTIMAL
p=k!Q+q-Q
r d,r out
+Q)
ind
112 a) CONTROLLER-DESIGN
In the following, the development of a multi-
whereby variable pressure and flow controller for a
pyrolysis reactor, aiming at removal the pressure
QDU t= AlII)' ~
r ou t
(12 b) shock, due to the transient exothermic state of
the reactor, is described.
q = AIy) . rp-;.If-
re
pr (12 c) Continuous-time PlO Control With Heuristically
Selected Controller Parameters
and
In order to get a justification for further ana-
lysis, digiti zed form of continuous-time PlO and
Q=flT,p) (12 d) PI pressure and flow controllers, respectively,
d,r r
the parameters of which have been heuristically
holds. selected, has been implemented in process control
computer, shown in the lower part of Fig. 1. From
In the eqs. (12a) to (12d), q is a hot gas flow the results, presented in Fig. 3, the two-input,
for direct heating of the material to be pyro- two-output process can be eventually stabilized
lized. This gas is driven by the pressure Pre f for re 1 atively large input changes, despite of
neglection of nonlinear character of the plant,
and is controlled via position y of respective and disregarding the pyrolysis kinetics. However
valve. Qdir and Qi~d describe the pyroly s is in order to guarantee some pre-defined quality ,
yield flow caused by direct and indirect heating, of stability, a systematic controller-design has
respectively. In the first phase of model buil- to be used.
ding Qind will be assumed to be constant. Further- Controller Design for Two-Input, Two-Output Plant
more, the eq. (12d ) is a consequence of the pyro-
lysis kinetics developed in the last section, Control-strategy for non-linear plant. In spite
whereby Qout is the assumed total reactor out- of the nonllnearltles In the plant dynamics,
linear controller-design shall be used for reasons
flow at atmospheric pressure Pou t. Pr is the of simplicity. This implies the use of the ade-
reactor pressure, controlled by output valve quate linearized version of the mathematical model
pos ition x, and T represents the process tempera- (11) at each temporary actual operating point. If
ture In the reactor. Finally, K is a constant the assumption of small deviations around the
factor of suitable unit. operating point does no longer hold, for instance
due to the time-variant pyrolysis kinetics, a
For small deviations of system variable s around switch-over to a suitable operating point model
the operating pOint, equations (1 2) become has to be carried out by a respective parameter
scheduling algorithm. Global stability can be
(13 ) guaranteed by a supervision algorithm, switching
to a robust controller, if necessary.
~~:L-~__~__L-~__ L-~ ~~
and D. Popovic (1985). Modelluntersuchungen
zur Bindung saurer Gase in Brennstoff aus -L__ __
Mull. Mull und Abfall, 17, pp. 258-268.
Thiele, G. (1979). Zur IdenTIfi kation rnit Hilfe o 2 4 6 8 10 12 14 16
des Prony-Verfahrens bel fehlerbehafteten Time(s)
Messungen. FS Dynamlsche Systeme, UnIversity
of Bremen, Report No. 8.
VDI (1985). Statusbericht Thermische Verfahren
der Abfallwlrtschaft o VDI-Gesellschaft
Energletechnlk, Bonn. pp. 1-390.
60
40 q
~~~~~~~~~~
2 4 6 8 10 12 14 16
Time(s)
Fig. 3. Step responses of pressure p (a) and flow
q (b) dynamics of pyrolysis reactor with
L-________ J
Process Con tr ol Com puter
6q
llq
Fig. 4. Parameter-estimation in the first itera-
f I0 ... - contro l- la op tion-step of controller-design.
r----------
Fig. 8. Response of the open-loop ~ re s sure sub-
system with respect to a x-input step
corresponding to a pressure-step of
20 47V_ 20 mbar.
W(kl
~ lI~
[mbar1
Fig. 7. Plant gain (k s ) and plant time-constant 20 % O. 222 sec 0.07 sec 0 . 400 sec
(T,) of pressure sub-system as a function 40 % 0.222 sec 0. 0 7 spc 0. 74 0 s ec
of percentage of full-scale reactor 60 % 0 .222 sec 0 .07 sec 1. 0 75 s ec
pressure (100% ~ 200 mbar). 0.22 2 sec 0 . 0 7 sec 1. 4 70 sec
80 %