A closed loop identi®cation method of Hammerstein model for continuous bioreactor with input multiplicity is proposed. Hammerstein model consists of nonlinear steady-state gain followed by a unity gain linear system. The method consists of ®rst getting local ®rst order plus time delay (FOPTD) models around the two input multiplicity values of the substrate feed concentration. The model parameters of the FOPTD is identi®ed by a least square optimization method. The initial guess for the model parameters are obtained from the settling time, the initial delay in the closed loop servo response and using a simple proportional controller formula. From the local process gain values obtained for the several step changes around the two operating conditions, the nonlinear gain portion of the Hammerstein is then obtained. The actual nonlinear gain and the identi®ed nonlinear gain is compared.List of symbols D dilution rate, h À1
A steady-state nonlinear feedforward controller (FFC) for measurable disturbances is designed for a continuous bioreactor, which is represented by Hammerstein type nonlinear model wherein the nonlinearity is a polynomial with input multiplicities. The manipulated variable is the feed substrate concentration (S f ) and the disturbance variable is the dilution rate (D). The productivity (Q=DP) is considered as the controlled variable. The desired value of Q=3.73 gives two values of feed substrate concentration. The nonlinearity in the gain is considered for relating output to the manipulated variable and separately for the relation between output to disturbance variable. The FFC is also designed for the overall linearized system. The performance of the FFC is evaluated on the nonlinear differential equation model. The FFC is also designed for the model based on a single nonlinear steady-state equation containing both D and S f . This nonlinear FFC gives the best performance. The nonlinear FFC is also designed by using only linear gain for the disturbance and nonlinear gain for the manipulated variable. Similarly, nonlinear FFC is also designed by using linear gain for the manipulated variable and the nonlinear gain for the disturbance variable. The performances of these FFC schemes are compared.List of symbols a 1 , a 2 de®ned by Eq. (20g) and Eq. (20h), respectively A, CThe denominator polynomials of the process and the disturbance model b 1 , b 2 de®ned by Eq. (20e) and Eq. (20f), respectively BThe numerator polynomial of the process c 1 , c 2 de®ned by Eq. (22a) and Eq. (22b), respectively D dilution rate (h ±1 ) D s steady-state value of D (g/L) G(z) output of the nonlinear gain system (block 4) g(z)G(z) ±Y s h 1 to h 4 de®ned by Eq. (20a) to Eq. (20d) K I substrate inhibition constant (g/L) K m substrate saturation constant (g/L)K p linear gain relating y to u K v linear gain relating y to v P product concentration (g/L) P m product saturation constant (g/L) Q product cells produced per unit time (g/L h) r 1 , r 2 de®ned by Eq. (22c) and Eq. (22d), respectively RThe numerator polynomial of the disturbance modelinput of the linear system (block 2) Y steady-state value of output y deviation value of the output y 1 output of the linear subsystem (block 4) X biomass concentration (g/L) a, b, d, coeffcients of linear discrete models [refer toEqs. (8a, 8b) and (9a, 9b)] r product yield parameter (g/g) w product yield parameter (h ±1 ) l speci®c growth rate (h ±1 ) l m maximum speci®c growth rate (h ±1 ) D deviation from the steady-state c yield factor for cell mass (g/g)
IntroductionThe dynamics of bioreactors are represented by nonlinear differential-equation models. The design of linear feedforward controller (FFC) to compensate for the effect of measurable disturbances of linear systems is a well-developed ®eld [1,2]. The performance of the linear controller is adequate for linear or mildly nonlinear systems. However, for highly nonlinear systems, the performance of the linear controller will not be satisfactory....
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.