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Azeotropic feed composition

From Eq.(7-2I), an azeotropic feed composition is such that... [Pg.249]

Figure 7-2 includes some representative copolymer-feed composition curves for r, varying with rj constant at 0.8. Azeotropic feed compositions containing appreciable quantities of both polymers can be achieved only when the reactivity ratio values are close to each other. [Pg.249]

Azeotropic feed compositions can exist in terpolymerizations if 5, Z and R [Eq. (7-47a-c)] have the same sign and are different from zero. The azeotropic... [Pg.257]

In the Type II case, the copolymerization tends toward an alternating arrangement of monomer units. Curve II of Figure 1 shows an example of an alternating copolymer that has an azeotropic copolymer composition, ie, a copolymer composition equal to the monomer feed at a single monomer feed composition. This case is analogous to a constant Foiling mixture ia vapor—Hquid equihbria.T) III... [Pg.178]

Hquid—Hquid-phase spHt the compositions of these two feed streams He oa either side of the azeotrope. Therefore, column 1 produces pure A as a bottoms product and the azeotrope as distillate, whereas column 2 produces pure B as a bottoms product and the azeotrope as distillate. The two distillate streams are fed to the decanter along with the process feed to give an overall decanter composition partway between the azeotropic composition and the process feed composition according to the lever rule. This arrangement is weU suited to purifying water—hydrocarbon mixtures, such as a C —C q hydrocarbon, benzene, toluene, xylene, etc water—alcohol mixtures, such as butanol, pentanol, etc as weU as other immiscible systems. [Pg.193]

If the feed rate is decreased, the trends of curves in Fig. 13-109 are reversed. The disturbance of other variables such as feed composition, boil-up ratio, and recycle of water-rich effluent from the decanter produces similar shifts in the steep concentration fronts, indicating that azeotropic towers are among the most sensitive separation operations, for which dynamic studies are essential if reli-... [Pg.1346]

In cases where rAB>l and rBA>l or rAB<.l and rBAazeotropic composition1 or critical point where the copolymer composition will exactly reflect the monomer feed composition (Figure 7.1). [Pg.341]

In the manufacture of aniline from nitrobenzene the reactor products are condensed and separated into an aqueous and organic phases in a decanter. The organic phase is fed to a striping column to recover the aniline. Aniline and water form an azeotrope, composition 0.96 mol fraction aniline. For the feed composition given below, make a mass balance round the column and determine the stream compositions and flow-rates. Take as the basis for the balance 100 kg/h feed and a 99.9 percentage recovery of the aniline in the overhead product. Assume that the nitrobenzene leaves with the water stream from the base of the column. [Pg.59]

If the composition (or flow-rate) of one stream is fixed by internal or external constraints, this may fix the composition and flows of other process streams. In Chapter 1, the relationship between the process variables, the design variables and design equations was discussed. If sufficient design variables are fixed by external constraints, or by the designer, then the other stream flows round a unit will be uniquely determined. For example, if the composition of one product stream from a distillation column is fixed by a product specification, or if an azeotrope is formed, then the other stream composition can be calculated directly from the feed compositions see Section 2.10. The feed composition would be fixed by the outlet composition of the preceding unit. [Pg.144]

Azeotropic and extractive distillation Distillation processes Extractive distillation(s) argon, 13 460 for aroma isolation, 11 519 atmospheric, 13 646 batch versus continuous, 3 780 of coal-tar naphthalene, 17 78-79 corrosion, 3 779-780 of crude oil, 12 401-402 13 593 debottlenecking, 13 521 in fatty acid neutralization, 22 740 favorable vapor-liquid equilibria, 3 778 feed composition, 3 778 general separation heuristics for, 22 316-317... [Pg.282]

The plots in Fig. 6-2 illustrate an interesting characteristic of copolymerizations with a tendency toward alternation. For values of r and r2 both less than unity, the F /f plots cross the line representing F — j. At these interesections or crossover points the copolymer and feed compositions are the same and copolymerization occurs without a change in the feed composition. Such copolymerizations are termed azeotropic copolymerizations. The condition under which azeotropic copolymerization occurs, obtained by combination of Eq. 6-12 with d[Mi]/ii[M2] = [Mi]/[M2], is... [Pg.474]

Corresponding data for the alternating radical copolymerization of styrene (Mi)-diethyl fumarate (M2)(n = 0.30 and r2 = 0.07) are shown in Figs. 6-6 and 6-7. This system undergoes azeotropic copolymerization at 57 mol% styrene. Feed compositions near the azeotrope yield narrow distributions of copolymer composition except at high conversion where there is a drift to pure styrene or pure fumarate depending on whether the initial feed contains more or less than 57 mol% styrene. The distribution of copolymer compositions becomes progressively wider as the initial feed composition differs more from the azeotropic composition. [Pg.477]

Fig. 2. Methyl ethyl ketone (MEK)—methyl isopropyl ketone (MIPK)—water system where A1 and A2 represent two different azeotropes FI, F2, and F3, different feed compositions Bn and Dn the corresponding bottoms and distillates, respectively (—-), the distillation boundary and ( ), the reachable compositions for the various feeds (a) approximate bow-tie and (b) exact reachable compositions. Fig. 2. Methyl ethyl ketone (MEK)—methyl isopropyl ketone (MIPK)—water system where A1 and A2 represent two different azeotropes FI, F2, and F3, different feed compositions Bn and Dn the corresponding bottoms and distillates, respectively (—-), the distillation boundary and ( ), the reachable compositions for the various feeds (a) approximate bow-tie and (b) exact reachable compositions.
The number of plates (defining the column configuration), feed, feed composition, column holdup, etc. for the problem are given in Table 4.9 (Chapter 4). The vapour-liquid equilibrium data and the kinetic data are taken from Simandl and Svrcek (1991) and Bogacki et al. (1989) respectively and are shown in Table 4.10 (Chapter 4). The vapour and liquid enthalpies are calculated using the data from Reid et al. (1977). As mentioned in Chapter 4, these data do not account for detailed VLE calculations and for any azeotropes formed. [Pg.277]

Even in the first publications concerning the copolymerization theory [11, 12] their authors noticed a certain similarity between the processes of copolymerization and distillation of binary liquid mixtures since both of them are described by the same Lord Rayleigh s equations. The origin of the term azeotropic copolymerization comes just from this similarity, when the copolymer composition coincides with monomer feed composition and does not drift with conversion. Many years later the formal similarity in the mathematical description of copolymerization and distillation processes was used again in [13], the authors of which, for the first time, classified the processes of terpolymerization from the viewpoint of their dynamics. The principles on which such a classification for any monomer number m is based are presented in Sect. 5, where there is also demonstrated how these principles can be used for the copolymerization when m = 3 and m = 4. [Pg.4]

The instantaneous copolymer composition X generally doesn t coincide with the monomer feed composition x from which the copolymer was produced. Such a coincidence X = x can occur only under some special values of monomer feed composition x, called azeotropic . According to definition these values can be calculated in the case of the terminal model (2.8) from a system of non-linear algebraic equations ... [Pg.23]

The solution of Eq. (8.1) permits to establish the dependence of the copolymer composition X prepared in CSTR on conversion p and xm. This dependence, generally speaking differs from calculated for the batch reactor through Eqs. (5.2) and (5.7). This difference would be largest in the range of middle conversions, since in the vicinity of extreme values p = Oandp = 1, the copolymer compositions (which are equal to m(xin) and xin, respectively) are the same for both reactors. It is of a certain interest that if xin = x, when the monomer feed composition at the reactor input is azeotropic (see Sect. 4.5), the copolymer composition X = x ... [Pg.87]


See other pages where Azeotropic feed composition is mentioned: [Pg.594]    [Pg.434]    [Pg.141]    [Pg.473]    [Pg.305]    [Pg.392]    [Pg.594]    [Pg.434]    [Pg.141]    [Pg.473]    [Pg.305]    [Pg.392]    [Pg.194]    [Pg.196]    [Pg.1248]    [Pg.1302]    [Pg.1310]    [Pg.1311]    [Pg.1312]    [Pg.1313]    [Pg.475]    [Pg.446]    [Pg.517]    [Pg.520]    [Pg.520]    [Pg.82]    [Pg.458]    [Pg.24]    [Pg.78]    [Pg.81]    [Pg.81]    [Pg.188]    [Pg.356]    [Pg.6]    [Pg.71]    [Pg.77]   
See also in sourсe #XX -- [ Pg.592 ]




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