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Other Control Structures

There are other control stmctures that one might think would work, but the two discussed below are shown to not handle the turndown problem. [Pg.439]


We could easily propose many other control structures for this pro-... [Pg.44]

This same problem exists in the other control structures, but in CSl, the increase in feed flow rate is accompanied by an immediate increase in reflux flow rate. This quickly affects Stage 8 temperature, and reboiler heat input increases in time to limit the peak in the propane impurity in the bottoms to about 1.5mol%. [Pg.205]

The variability in the vapor distillate flow rate is still much less than with the other control structures, so even with dual-composition control, the downstream unit is not subjected to large and rapid disturbances. [Pg.209]

In the above series, an important paper of Tyreus and Luyben [5] deals with second-order reactions in recycle systems. Two cases are considered complete one-pass conversion of a component (one recycle), and incomplete conversion of both reactants (two recycles). As general heuristic, they found that fixing the flow in the recycle might prevent snowballing. In the first case, the completely converted component could be fed on flow control, while the recycled component added somewhere in the recycle loop. In the second case, the situation is more complicated. Four reactant feed control alternatives are proposed, but only two workable. This is the case when both reactants are added on level control in recycles (CSl), or when the reactant is added on composition control combined with fixed reactor outlet (CS4). As disadvantage, the production rate can be manipulated only indirectly. Other control structures - with one reactant on flow control the other being on composition (CS2) or level control (CS3) - do not work. The last structure can be made workable if the recycle flow rates are used to infer reactant composition in the reactor. This study reinforces the rule that the flow rate of one stream in a liquid recycle must be fixed in order to prevent snowballing. [Pg.404]

The control structure for the chlorobenzene system is given in Figure 11.26. Two features are different from the other control structures. They involve the use of steam-to-feed ratios. In both columns, the reboiler heat input is ratioed to the feed to the column. These are added to improve the load response of the system that was found to be inferior to those found in the other solvent systems. The feed flow is measured and sent to a multiplier block. The other input to the multiplier is the output signal from the temperature controller. The output of the multiplier sets the reboiler heat input. So the temperature controller is looking at temperature and outputting a ratio signal. Controller parameters are given in Table 11.6. Notice that the Qr/F ratios must be in units of GJ per kmol in the Aspen Dynamic convention. [Pg.360]

Luyben (1994) has investigated these and similar relations for more complex reaction kinetics over a wide range of the disturbances (Fq and zo)- The snowball effect is not an artifact of the simplifying assumptions employed (e.g., perfect composition control in the column). It appears to be a general effect in recycle systems that can arise from inadequate reactor holdup or a particular choice of the plant inventory/flow control structure. However, before attempting to generalize, we look at two other control structures and their sensitivity characteristics. [Pg.542]

Pioneering work in living anionic copolymerization of siloxanes was reported by Morton and co-workers 139 140, who synthesized isoprene-dimethylsiloxane block copolymers utilizing D4 as the siloxane monomer. The use of D3 in the synthesis of siloxane block copolymers with controlled structures was demonstrated by Bostick and others. Excellent reviews of these earlier studies and subsequent developments are available in the literature 22 137 13S). [Pg.29]

Phenol, the simplest and industrially more important phenolic compound, is a multifunctional monomer when considered as a substrate for oxidative polymerizations, and hence conventional polymerization catalysts afford insoluble macromolecular products with non-controlled structure. Phenol was subjected to oxidative polymerization using HRP or soybean peroxidase (SBP) as catalyst in an aqueous-dioxane mixture, yielding a polymer consisting of phenylene and oxyphenylene units (Scheme 19). The polymer showed low solubility it was partly soluble in DMF and dimethyl sulfoxide (DMSO) and insoluble in other common organic solvents. [Pg.229]

The living radical polymerization of some derivatives of St was carried out. The polymerizations of 4-bromostyrene [254], 4-chloromethylstyrene [255, 256], and other derivatives [257] proceed by a living radical polymerization mechanism to give polymers with well-controlled structures and block copolymers with poly(St). The random copolymerization of St with other vinyl... [Pg.120]

Whether the design and construction of control rooms and other occupied structures, as well as detection, warning, and emergency response provisions, will provide adequate protection in the event of a major fire, explosion, or toxic release event Recommended distances for spacing of buildings and equipment... [Pg.99]

Two types of subnucleosomal particles which retain many, if not all, of the properties of the intact nucleosome have been identified. The first type contains only H3 and H4, either as a tetramer (Bina-Stein and Simpson, 1977) or an octamer (Simon et al., 1978 Stockley and Thomas, 1979), while the second contains all core histones, each lacking up to 30 amino-terminal residues which have been digested away by trypsin (Whitlock and Simpson, 1977). The fact that other subnucleosomal particles have not been isolated does not necessarily mean that they cannot exist it indicates only that the proper reconstitution or dissociation conditions have not been found. Nevertheless, results to date point to H3-H4 on the one hand, and the trypsin-resistant carboxy-terminal regions of all the core histones on the other hand, as playing controlling structural roles in the formation of the nucleosome and the consequent folding of the DNA. [Pg.29]

So the multiloop SISO diagonal controller remains an important structure. It is the base case against which the other structures should be compared. The procedure discussed in this chapter was developed to provide a workable, stable, simple SISO system with only a modest amount of engineering effort. The resulting diagonal controller can then serve as a realistic benchmark, against which the more complex multivariable controller structures can be compared. [Pg.595]


See other pages where Other Control Structures is mentioned: [Pg.174]    [Pg.431]    [Pg.439]    [Pg.439]    [Pg.441]    [Pg.142]    [Pg.36]    [Pg.174]    [Pg.431]    [Pg.439]    [Pg.439]    [Pg.441]    [Pg.142]    [Pg.36]    [Pg.2132]    [Pg.2489]    [Pg.27]    [Pg.277]    [Pg.1027]    [Pg.578]    [Pg.116]    [Pg.462]    [Pg.19]    [Pg.28]    [Pg.76]    [Pg.149]    [Pg.154]    [Pg.30]    [Pg.111]    [Pg.779]    [Pg.630]    [Pg.632]    [Pg.317]    [Pg.257]    [Pg.272]    [Pg.102]    [Pg.592]    [Pg.123]    [Pg.311]    [Pg.84]    [Pg.599]    [Pg.64]    [Pg.21]    [Pg.160]    [Pg.15]   


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Structural controllability

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