Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Component intermediate

As w as mentioned earlier, extra rows are provided as can be seen in Figure 1. This gives extra flexibility needed for process design case studies. Often, the set of case studies initially envisioned by the engineer or manager are not sufficient to answer all questions. The extra rows allow intermediate recycles or intermediate flows from or additions to the plant that might not have been envisioned initially. Another value of the intermediate rows is to provide component values at intermediate points in the process. The breakeven value of a proposed purchase stream from another plant would be one use of intermediate component values. [Pg.349]

It is the ultimate objective of a refinery to transform the fractions from the distillation towers into streams (intermediate components) that eventually become finished products. This also is where a refinery makes money, because only through conversion can most low-value fractions become gasoline. The most widely used conversion method is called cracking because it uses heat and pressure to "crack"... [Pg.202]

In almost all cases the molecules have a higher value as liquid than as gas. Crude oil streams typically contain a low percentage of intermediate components. Thus, it is not normally economically attractive to consider other alternatives to multistage separation to stabilize the crude. In addition, the requirement to treat the oil at high temperature is more important than stabilizing the liquid and may require the flashing of both intermediate and heavy components to the gas stream. [Pg.130]

Gas condensate, on the other hand, may contain a relatively high percentage of intermediate components and can be easily separated from entrained water due to its lower viscosity and greater density difference with water. Thus, some sort of condensate stabilization should be considered for each gas well production facility. [Pg.131]

The partial pressure at a given pressure and temperature is lower when there are more moles of other components in the gas phase. The lower the partial pressure the greater the tendency of the component to flash to gas. Thus, the higher the fraction of light components in the inlet fluid to any separator, the lower the partial pressure of intermediate components in the gas phase of the separator, and the greater the number of intermediate component molecules that flash to gas. [Pg.131]

Figure 6-1 shows a multistage separation process. By removing molecules of the light components in the first separator they are not available to flash to gas from the liquid in the second separator, and the partial pressure of intermediate components in the second separator is higher than it would have been if the first separator did not exist. The second separator serves the same function of increasing the partial pressure of the intermediate components in the third separator and so forth. [Pg.131]

Typically, the liquid out the bottom of the tower must meet a specified vapor pressure. The tower must be designed to maximize the molecules of intermediate components in the liquid without exceeding the vapor pressure specification. This is accomplished by driving the maximum number of molecules of methane and ethane out of the liquid and keeping a.s much of the heavier ends as possible from going out with the gas. [Pg.135]

At the lop of the tower any intermediate components going out with the gas are condensed, separated, pumped back to the tower, and sprayed down on the top tray. This liquid is called reflux. and the two-phase separator that separates it from the gas is called a reflux tank" or reflux drum. The reflux performs the same function as the cold feed in a cold-feed stabilizer. Cold liquids strip out the intermediate components from the gas as the gas rises. [Pg.137]

The heat required at the reboiler depends upon the amount of cooling done in the condenser. The colder the condenser, the purer the product and the larger the percentage of the intermediate components that will be recovered in the separator and kept from going out with the gas. The hotter the bottoms, the greater the percentage of light components will be boiled out of the bottoms liquid and the lower the vapor pressure of the bottoms liquid. [Pg.137]

A condensate stabilizer with reflux will recover more intermediate components from the gas than a cold-feed stabilizer. However, it requires more equipment to purchase, install, and operate. This additional cost must be justified by the net benefit of the incremental liquid recovery, less the cost of natural gas shrinkage and loss of heating value, over that obtained from a cold-feed stabilizer. [Pg.137]

The ROD is similar to a cold feed stabilizing tower for the rich oil. Heat is added at the bottom to drive off almost all the methane (and most likely ethane) from the bottoms product by exchanging heat with the hot lean oil coming from the still. A reflux is provided by a small stream of cold lean oil injected at the top of the ROD. Gas off the tower overhead is used as plant fuel and/or is compressed. The amount of intermediate components flashed with this gas can be controlled by adjusting the cold loan oil retlux rate. [Pg.245]

The two reactions are achieved in only one step without altering the product quality. The inhibition of enzymes by excess of intermediate components is reduced in this system. The presence of an organic solvent in the medium allows a high solubility of acylglycerols and a well-controlled partition of the components in the reactor. [Pg.579]

If the parameter lists of the output event differ from those of the input to which it is coupled, a mapping must be defined at the connector. If the transformation is too complex, an intermediate component should be defined for the purpose. [Pg.449]

While the resulting concentration profiles, and in particular the computed spectra, seem to be reasonably close to the true ones, there are significant discrepancies, typical for model-free analyses, (a) The computed concentration profile for the intermediate component reaches zero at the end of the measurement, (b) The initial part of the concentration profile for the final product is wrong it does not start with zero concentration. Both discrepancies are the result of rotational ambiguity. The minimal ssq, reached after relatively few iterations, reflects the noise of the data and not a misfit between CA and Y. ssq does not improve if the correct matrices C and A are used. [Pg.288]

In complex systems that involve multiple Fe-bearing species and phases, such as those that are typical of biologic systems (Tables 1 and 2), it is often difficult or impossible to identify and separate all components for isotopic analysis. Commonly only the initial starting materials and one or more products may be analyzed for practical reasons, and this approach may not provide isotope fractionation factors between intermediate components but only assess a net overall isotopic effect. In the discussions that follow on biologic reduction and oxidation, we will conclude that significant isotopic fractionations are likely to occur among intermediate components. [Pg.369]

Three products (PI, P2, aod P3) and two slop cuts (SI and S2) are produced. The average composition of the products are 95 mole percent. The PI product is mostly the lightest component (component 1). The P2 product is mostly intermediate component (number 2) with some impurities of both the light and the heavy components. The final product P3 is what is left in the still pot and on the trays. The times to produce the various products and slop cuts are given in the results shown in Table 5.14. The total time for the batch distillation in this example is 6.4 hours. [Pg.162]

Note that the 70.92 motes of the first slop cut contain mostly light and intermediate component (25/75 mol %), while the 34.5 moles of second slop cut contain mostly intermediate and heavy components (52/48 mol %). Recycling these slop cuts back to the next batch cycle makes little thermodynamic sense, but that is the normal procedure in practice. [Pg.162]

The vector of openloop transfer functions relating the controlled variables to the load disturbance (feed composition mole fraction of intermediate component) is ... [Pg.611]

Three thermally coupled schemes have been particularly analyzed. Two of them are fairly similar and make use of a main column and a side column. One can use a side extraction in the vapor phase from the first column and feed it to a side rectifier that purifies the intermediate component. The reboiler of the side column is eliminated by recycling the bottom stream, in the liquid phase, to the first column. The arrangement is known as a thermally coupled distillation system with a side rectifier (TCDS-SR), and its structure is shown in Figure la. If the side extraction from the first column is carried out in the... [Pg.54]

Dynamic Behavior of the Intermediate Component (Set Point Change)... [Pg.66]

Figure 7 shows the dynamic responses obtained when the set point for the intermediate component was changed from 0.98 to 0.984. One may notice the better response provided by the Petlyuk column in this case, which is faster than the other two systems and without oscillations. When the lAE values were calculated, a remarkable difference in favor of the Petlyuk system was observed 2.87 x 10 for the Petlyuk column, compared to 0.0011 for the PUL system and 0.0017 for the PUV system. The results from this test may seem unexpected, since the new arrangements have been proposed to improve the operation capabilities of the Petlyuk column. The SISO control of the intermediate component, interestingly, seems to conflict with that of the other two components in terms of the preferred choice from dynamic considerations. [Pg.66]

The results for this test and for the responses to disturbances in feed compositions of B and C are summarized in Table 4. A consistent trend with the servo tests was observed, in the sense that one option provides the best common choice for the control of the system under feed disturbances on the extreme components of the mixture, but a different arrangement yields a superior dynamic performance for the control task under a feed disturbance on the intermediate component. From Table 4, the lAE values indicate that the PUL system shows the best behavior for feed disturbances in the light and heavy component. However, the PUL arrangement shows the worst response when the feed disturbance in the intermediate component was considered, in which case both the Petlyuk and the PUV systems show fairly similar rejection capabilities. [Pg.67]

Fig. 7. Closed loop responses for a set point change in the composition of the intermediate component... Fig. 7. Closed loop responses for a set point change in the composition of the intermediate component...
Uses. Industrial solvent chemical intermediate component in inks and paints... [Pg.531]

It has been well recognized that the mixed-function oxidase system of Bacillus megaterium is involved in steroid hydroxylation (, as already described above. This enzyme system is composed of a NADPH-specific FMN flavoprotein (megaredoxin reductase), an iron-sulfur protein (megaredoxin) and cytochrome P cn. The megaredoxin protein plays an important role as an intermediate component of electron transfer from reduced flavoprotein to cytochrome P en. [Pg.124]

If produced gas is to be injected back into the producing formation or seme other formation, rather than delivered to a gas pipeline, it may be possible to inject the third product stream into the injection gas stream, or to inject it separately into the reservoir. However, this may be only a temporary solution to the problem, since the intermediate components could be reproduced again, and may be in higher concentrations than they were the first time. If injected gas is ultimately delivered to a gas pipeline, and if intermediate components have been injected also, the gas conditioning problem to meet dewpoint requirements will be more difficult at a later date. [Pg.78]

Then the minimum reflux and the distribution of the intermediate component are found from the two equations that result from substitution of the two values of 8 into Underwood s second... [Pg.397]

The transparency of the electrode also enables spectra to be recorded of electrogenerated species as well as of any species produced as a result of a homogeneous chemical reaction. Such spectra have been recorded with rapid scanning spectrometers that are capable of recording as many as 100 or more spectra per second in the UV-visible range [22]. Spectra can be useful for structural identification of intermediate components in the reaction sequence and for... [Pg.66]

Pibouleau et al. (1988) provided a more flexible representation for the synthesis problem by replacing the single reactor unit by a cascade of CSTRs. They also introduced parameters for defining the recovery rates of intermediate components into the distillate, the split fractions of top and bottom components that are recycled toward the reactor sequence, as well as parameters for the split fractions of the reactor outlet streams. A benzene chlorination process was studied as an example problem for this synthesis approach. In this example, the number of CSTRs in the cascade was treated as a parameter that ranged from one up to a maximum of four reactors. By repeatedly solving the synthesis problem, an optimum number of CSTRs was determined. [Pg.423]

Since we are interested in generating the maximal amount of the intermediate component B in the consecutive reaction A —> B —> C, we look at the concentration of B defined by xb v) in equation (4.82). This we do using the MATLAB function xBversusy.m. [Pg.188]

A classical approach72 to unravelling the mechanism of electrochemical reactions and to identifying the rate-determining step (RDS) is based on testing the validity of possible sequences of reaction stages according to the elementary theory of electron transfer. As opposed to disc voltammetry, one does not look for direct evidence such as the presence of intermediate components. As a consequence, more reaction sequences appear to be theoretically possible, which in the ideal case can be dismissed, all but one on the basis of experimental evidence. It should be pointed out that neither does the identification of intermediates by means of electrochemical or non-electrochemical techniques automatically lead to the true reaction mechanism. It is only an aid in the sense that identified intermediates must occur in a postulated reaction mechanism and that hence the number of possible mechanisms can be reduced. [Pg.104]


See other pages where Component intermediate is mentioned: [Pg.483]    [Pg.181]    [Pg.25]    [Pg.111]    [Pg.132]    [Pg.135]    [Pg.246]    [Pg.262]    [Pg.272]    [Pg.101]    [Pg.29]    [Pg.55]    [Pg.55]    [Pg.61]    [Pg.69]    [Pg.461]    [Pg.115]    [Pg.148]    [Pg.368]    [Pg.380]   
See also in sourсe #XX -- [ Pg.42 ]




SEARCH



Accumulation intermediate component

Intermediate components, multicomponent distillation

Ionic Components and the Reactive Intermediate Stages

Membranes intermediate components

Three-component mixtures intermediate section trajectories

© 2024 chempedia.info