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               310                                                                         Membranes, Synthetic, Applications


                                                                 portion of the conventional process with a pervaporation
                                                                 unit featuring water-selective membranes. Overhead va-
                                                                 por from the distillation section is condensed and fed to the
                                                                 membrane unit at a temperature slightly below the boiling
                                                                 point. Water pervaporates preferentially, leaving purified
                                                                 ethanol on the feed side. To supply the latent heat of vapor-
                                                                 ization, a pervaporation system is designed with reheaters
                                                                 between  succeeding  membrane  stages.  Industrially,
                                                                 pervaporation technology  for  ethanol/water  separation
                                                                 has matured rapidly. Modern pervaporation plants have
                                                                 capacities reaching several thousand tons per year.
                                                                   Separation of isopropanol (IPA) and water by perva-
               FIGURE  24  Hybrid  distillation–pervaporation  process  for  fer-  poration has also reached production scale. Much of the
               mentation ethanol production (E, ethanol).        current  capacity  is  devoted  to  azeotrope  breaking and
                                                                 dehydration  during  IPA  synthesis.  Recently,  anhydrous
               the technology since the beginning of the 1990s. Conven-  isopropanol  has become  a  preferred  drying  solvent  in
               tionally, anhydrous ethanol is produced by distilling dilute  the semiconductor industry, where chip wafers are first
               alcohol from about 10% (e.g., that from biomass fermen-  washed with ultrapure water, then rinsed with the alcohol
               tation) to about 90%, then further dehydrating to 99+%  to promote uniform drying. The water-laden isopropanol
               ethanol by means of azeotropic distillation or extractive  generated can be conveniently reused after dehydration
               distillation. Dehydration requires additional columns, be-  by pervaporation. Unlike with pressure-driven membrane
               sides the main rectification tower and the use of entrainers  processes such as RO or UF, particulates and nonvolatile
               to  break  the  azeotrope.  Although  distillation  enriches  substances such as salts are not carried over during per-
               ethanol efficiently from low to moderately high concentra-  vaporation. This helps maintain the effectiveness of con-
               tions (ca. 80%) in a small number of equilibrium stages, it  tamination control.
               becomes increasingly energy-intensive as the azeotropic  Pervaporation technology has matured considerably
               point is approached. The hybrid system shown conceptu-  over the past two decades. Increasing numbers of applica-
               ally in Fig. 24 replaces the energy- and capital-intensive  tions have been identified, such as those listed in Table VII.



                            TABLE VII  Products Separated or Purified by Pervaporation (Source: Sulzer Chemtech Ltd.,
                            Winterthur, Switzerland)
                            Alcohols                           Esters
                              Methanol                 CH 4 O   Methyl acetate (MeAc)       C 3 H 6 O 2
                              Ethanol                 C 2 H 6 O  Ethyl acetate (EtAc)       C 4 H 8 O 2
                              Propanol (both isomers)  C 3 H 8 O  Butyl acetate (BuAc)      C 6 H 12 O 2
                              Butanol (all isomers)   C 4 H 10 O  Ethers
                              Pentanol (all isomers)  C 5 H 12 O  Methyl tert-butyl ether (MTBE)  C 5 H 12 O
                              Cyclohexanol            C 6 H 12 O  Ethyl tert-butyl ether (ETBE)  C 6 H 14 O
                              Benzyl alcohol          C 7 H 8 O  Di-isopropyl ether (DIPE)  C 6 H 14 O
                            Ketones                             Tetrahydro furan (THF)       C 4 H 8 O
                              Acetone                 C 3 H 6 O  Dioxane                    C 4 H 8 O 2
                              Butanone (MEK)          C 4 H 8 O  Organic acids
                              Methyl isobutyl ketone (MIBK)  C 6 H 12 O  Acetic acid        C 2 H 4 O 2
                             Aromatics                         Nitriles
                              Benzene                   C 6 H 6  Acetonitrile                C 2 H 3 N
                              Toluene                   C 7 H 8  Aliphatics             From C 3 to C 8
                              Phenol                  C 5 H 6 O  Chlorinated hydrocarbons
                            Amines                              Dichloro methane             CH 2 Cl 2
                              Triethylamine           C 6 H 15 N  Perchloroethylene           C 2 Cl 4
                              Pyridine                C 6 H 5 N
                              Aniline                 C 6 H 7 N
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