Page 232 - Academic Press Encyclopedia of Physical Science and Technology 3rd Chemical Engineering
P. 232

P1: GJC Final Pages
 Encyclopedia of Physical Science and Technology  EN004E-182  June 8, 2001  18:16






               556                                                                                       Distillation


                                                                 cuts can be taken to obtain lower volatility products. Inter-
                                                                 mediate cuts of mixed composition are sometimes taken
                                                                 between each product cut, and these are saved and later
                                                                 returned to the still pot for inclusion in the next batch.


                                                                 C. Extractive and Azeotropic Distillation
                                                                 Conventional distillation tends to be difficult and uneco-
                                                                 nomical because of the large number of stages required
                           FIGURE 15 Flash distillation.         when the relative volatility between the components to be
                                                                 separated is very low. In the extreme case, in which an un-
               vessel. The temperature and pressure of the liquid entering  wanted azeotrope is formed, distillation past the azeotrope
               the flash vessel are adjusted to achieve the required degree  becomes impossible. Extractive or azeotropic distillation
               of vaporization. The compositions of the product streams  can sometimes be used to overcome these difficulties.
               leaving the flash vessel are different and are a function of  Both processes involve the addition of a new material,
               the extent to which vaporization occurs.          the solvent, to the mixture. The solvent is chosen so as
                 Although the flash vessel itself is simple, care must be  to increase the relative volatility of the components to
               taken to ensure that the resultant vapor and liquid phases  be separated. During extractive distillation, the solvent is
               are separated completely from one another. To this end,  generally added near the top of the column, and because
               the entering feed is often introduced tangentially rather  it has a low volatility it is withdrawn with the product at
               than at a 90-degree angle to the vessel wall. An annu-  the bottom. In azeotropic distillation, the solvent is with-
               lar baffle directs the liquid droplets that are created by  drawn as an azeotrope with one or more of the components
               the flash toward the bottom of the vessel. By installing a  to be separated—usually in the overhead product. If the
               wire mesh (approximately 75 mm thick) near the top of  ratio of the components to be separated is different in the
               the vessel, fine liquid drops are prevented from leaving the  withdrawn azeotrope from their ratio in the feed to the col-
               top of the vessel as entrainment in the high-velocity vapor  umn, then at least a partial separation has been achieved.
               stream.                                           In both processes it is necessary to separate the solvent
                 At best, only one theoretical stage is achieved by a flash  from the product. This can be accomplished, for exam-
               distillation; however, it is used frequently in cryogenic and  ple, by distillation, solvent extraction, or even gravity set-
               petroleum processing applications, where its simplicity is  tling, depending on the characteristics of the components
               often attractive for nondemanding separations. Flashing  involved.
               often occurs in conventional distillation columns as feed
               and reflux streams enter. This flashing must be considered
               when column entrance devices and distributors are being  D. Reactive Distillation
               designed.                                         Many distillation columns reside upstream or downstream
                                                                 of catalytic reactors. Over the last decade, catalysts have
               B. Batch Distillation

               Batch distillation (Fig. 16) is often preferable to contin-
               uous distillation when small quantities of feed material
               are processed. A liquid feed is charged to a still pot and
               heated until vaporization occurs. Vapor leaves the top of
               the column, and after condensation, part is removed as
               product and the rest returned to the column as reflux. As
               distillation proceeds, the contents of the still pot and the
               overhead product become richer in less volatile compo-
               nents. When operated at a fixed reflux ratio, an overhead
               product cut is collected until the product composition be-
               comes unaccceptable. As an alternative, the reflux ratio
               can be gradually increased to hold the product composi-
               tion constant as the cut is taken. For a fixed rate of heat
               addition to the still pot, the latter option results in a steadily
               declining product flow rate. After the first cut, subsequent    FIGURE 16 Batch distillation.
   227   228   229   230   231   232   233   234   235   236   237