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Pl controllers

M. Perez and P. Albertos. Self-oscillating and chaotic behaviour of a Pl-controlled CSTR with control valve saturation. J. Process Control, 14 51-57, 2004. [Pg.274]

Hemal AK, Vaidyanathan S, Sankaranarayanan A, Ayyagari S, Sharma PL. Control of massive vesical hemorrhage due to radiation cystitis with intravesical instillation of 15 (s) 15-methyl prostaglandin F2-alpha. Int J Clin Pharmacol Ther Toxicol 1988 26(10) 477-8. [Pg.110]

Fig. 6. (A) El binding assay. Lane M contains the input 32P-labeled DNA fragments from pKS+ ori. These fragments were incubated with 100 pL TNT lysate containing either no El protein (-), EE-E1 protein (El with an EE epitope fused at the N-terminus), or wild-type El. DNA-protein complexes were immunoprecipitated with either El -specific antiserum (SSQN) or EE-specific antibody. El-bound DNA was extracted and analyzed by gel electrophoresis (option 1). (B) E1-E2 cooperative binding assay. Lane M contains the input 32P-labeled DNA fragments from pKS+ ori. These fragments were incubated with 50 pL control TNT lysate (lane 1), 25 pL El lysate and 25 pL control lysate (lane 2) and 25 pL El lysate and 25 pL control lysates (lanes 3-6). Lane 3 contains wild-type E2 protein and lanes 4-6 contain E2 proteins with deletions in the hinge region (15). DNA-protein complexes were immunoprecipitated with El-specific antiserum (SSQN), and El-bound DNA was extracted and analyzed by gel electrophoresis (option 2). Fig. 6. (A) El binding assay. Lane M contains the input 32P-labeled DNA fragments from pKS+ ori. These fragments were incubated with 100 pL TNT lysate containing either no El protein (-), EE-E1 protein (El with an EE epitope fused at the N-terminus), or wild-type El. DNA-protein complexes were immunoprecipitated with either El -specific antiserum (SSQN) or EE-specific antibody. El-bound DNA was extracted and analyzed by gel electrophoresis (option 1). (B) E1-E2 cooperative binding assay. Lane M contains the input 32P-labeled DNA fragments from pKS+ ori. These fragments were incubated with 50 pL control TNT lysate (lane 1), 25 pL El lysate and 25 pL control lysate (lane 2) and 25 pL El lysate and 25 pL control lysates (lanes 3-6). Lane 3 contains wild-type E2 protein and lanes 4-6 contain E2 proteins with deletions in the hinge region (15). DNA-protein complexes were immunoprecipitated with El-specific antiserum (SSQN), and El-bound DNA was extracted and analyzed by gel electrophoresis (option 2).
Try to improve the value of the objective function by using a Pl-controller to maintain constant selectivity throughout the batch, where... [Pg.419]

Pl-control loop I xnampulated variable=Ta controlled variable = T... [Pg.577]

PI is the most used controller. The tuning consists of a Pl-controller the finding the dynamic characteristics called ultimate gain (/C ) and ultimate period (Py). A step disturbance is introduced, and the gain of controller in P mode is slowly increased. The value where sustained bounded oscillations appear designates the ultimate gain K. The ultimate period can be measured directly. [Pg.132]

The tuning may follow a simplified procedure. Let Af ax and Awmax be the maximum allowed control error and control action, respectively. Then the variable ranges are y and u Au, Pl-controllers are used, with the gain Kf = A iax / Af ax) and integration time TI = 20 min. Table 17.9 presents the nominal operating point of the three controllers, at a nominal toluene plant throughput of 125 kmol/h. [Pg.652]

The nature of long-wavelength luminescence that looks rather similarly for all samples can be assigned to cationic defects, more probable, within the particles since this PL is also explicitly x-dependent. The defects can play a role of photoelectron captures, however, a disorder in the mixed phases is a reason of the radiationless relaxation. The research is of importance for understanding features of the ternary semiconductor nanophases and as a tool of PL control in semiconductor-doped glasses. [Pg.319]

In the previous case study, the focus was on control structure selection. As control algorithms standard linear Pl-controllers were used. In a second case study, the focus is on control algorithms. For that purpose we compare different control algorithms for a fixed control stmcture. The process to be considered is an industrial benchmark problem, which was treated in joint research with Bayer AG [21, 33]. The process and its open loop dynamic behavior is illustrated in Fig. 10.29. Components B and C are the reactants. They react in two consecutive equilibrium reactions to products A and E. The main product E is obtained in the bottoms of the column and the other product A in the distillate. [Pg.274]

In (12.5) the quotient Qi resulting from the system pressure Ptotai divided by pressure drop Api has no dimension and thus is not influenced by any fluidic parameters that is, it remains constant during a gradient run. Because of its direct proportionahty to the fluidic resistance of a specific branch, it serves as a perfect regulating variable in the Pl-control circuit, which is now also apphcable for gradient HPLC systems. [Pg.312]

Tuning of single-input, single-output (SISO) controllers (P, PI, and PID controllers). Note that Section 21.4 provides instruction on model-based Pl-controller tuning. [Pg.705]

For more details on the implementation and tuning of PI controllers using HYSYS.Plant, the reader is referred to the multimedia CD-ROM that accompanies this text (HYSYS - Dynamic Simulation Tuning PI Controllers). In the following case studies, C R analysis is demonstrated, with results verified using d)mamic simulations of the Pl-controlled processes. [Pg.736]

Second, the perfect control assumption results in an umealistic estimation of the expected economic penalty. The multiloop-PI based methodology offers the more realistic estimation of the economic penalty. This is due the fact that the estimated economic penalty is related to the realisability of the controller used. Both perfect controller and OSOF controller are hardly realisable and are equivalent, to some extent, to high gain output feedback control. The multiloop-Pl controller, on the other hand, is based on realistic estimations of the control action since they are based on the nonlinear response of the system and well established tuning techniques. [Pg.237]

In the control design phase, the controller structure must be determined, e.g. the decision must be made whether a simple control structure with independent Pl-controllers is specified and realized at fairly low cost, whether switching and gain scheduling of controllers has to be considered, or whether a demanding (and costly) project on nonlinear model-based control of the process should be set up. We call the second type of questions controller structure selection. Using the tools presented in this chapter much can be said about the necessary type of the controller before designing it. [Pg.431]

First, full matrix PI controllers were designed for these control structures. The simulations confirm the predictions made before. The control structures 142 and 143 nearly achieve the desired performance (Fig. 9). The plot of the simulation of structure 143 is omitted here because of the limit of space. The structures 642 and 643 on the other hand are not able to achieve the required performance with a low-order controller, as shown in Figure 10. The control structure 142 achieves good results even with a decentralized (noninteracting) PI-controller (three Pl-controllers on the main diagonal), although the third output is slower and shows a larger overshoot than predicted (Fig. 9). The control of the other structures with a decentralized controller was not possible. Similar results for the structures 142 and 642 for lower bandwidths were shown in [40]. Additional simulation results were also shown in [27, 28]. [Pg.452]

Fig. 9. Simulation of CS142 with full PI controller (left), and decentralized Pl-controller (right). Dotted off-diagonal elements. Fig. 9. Simulation of CS142 with full PI controller (left), and decentralized Pl-controller (right). Dotted off-diagonal elements.
Add 100 pL control and patient plasma or serum to microcentrifuge tubes (see Note 1). [Pg.180]

Integrity of SRP/CS and safety function is expressed in terms of performance levels (PLs). Control risk assessment is used to determine the required PL (PLr) using a risk graph see Figure 9.5. [Pg.171]

For this purpose, a Pl-controller is designed which controls the simulated product quality by manipulating the reflux fraction i . Similar to the experimental set up, the controller was switched on if the deviation was less than 0.002 from setpoint. [Pg.435]


See other pages where Pl controllers is mentioned: [Pg.33]    [Pg.74]    [Pg.282]    [Pg.347]    [Pg.1166]    [Pg.294]    [Pg.1347]    [Pg.385]    [Pg.734]    [Pg.83]    [Pg.643]   
See also in sourсe #XX -- [ Pg.205 ]




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