Page 388 - Analysis, Synthesis and Design of Chemical Processes, Third Edition
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2.   If the azeotrope is a binary, heterogeneous azeotrope, that means there is a region where the two
                                components  form  two  mutually  immiscible  liquid  phases  (both  in  equilibrium  with  the
                                azeotropic  vapor  composition,  which is  between  the  two  liquid  compositions),  and  hence  a
                                phase separator and a second column are added. The phase separator provides one phase on the
                                other  side  of  the  azeotrope  from  the  feed,  so  that  phase  can  be  purified  by  distillation  in  a
                                second column (Figure 12.4[b]).

                          3.   If the azeotrope concentration is pressure sensitive, one column is used to distill close to the
                                azeotrope. One “pure” component is produced from the bottom of this first column. Then the
                                pressure of the distillate is raised so that the azeotropic composition is now below the distillate
                                composition.  Then  a  second  column  is  used  to  purify  the  second  component.  Because  the
                                volatility switches as the azeotrope is crossed, the second component is in the bottom stream of
                                the second column (Figure 12.4[c]). This particular sequence assumes that the azeotrope is less
                                concentrated in A at higher pressures.
                          4.   A third component can be added to change the phase behavior. This method is discussed in the
                                next section.


                    The first alternative is illustrated in Figure 12.4(a). Here, a distillation column is used that will provide
                    “pure” B in the bottoms and a near-azeotropic mixture in the distillate. The McCabe-Thiele construction
                    for this distillation column is illustrated in Figure 12.5(a). Then a different type of separation is used to
                    purify Component A (not shown on the McCabe-Thiele diagram). The impure stream from the second
                    separator should be recycled, if possible; however, treatment as a waste stream is also possible. The
                    recycle stream will most likely be fed to a different tray from the feed stream, because distillation column

                    feeds should always be near the point in the column with the same concentration as the feed stream.

                    Figure 12.5 McCabe-Thiele Diagrams for Distillation Arrangements in Figure 12.4
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