Page 143 - Adsorption Technology & Design, Elsevier (1998)
P. 143

132  Processes and cycles


              Common examples of thermal swing adsorption include solvent recovery
            with activated carbons, and drying of gases or liquids with type A  zeolites.
            Drying of organic vapours using type A zeolites can overcome the difficulty
            in distillation  of reaching  high purities  in chemical  systems which contain
            vapour-liquid azeotropes. All these processes can be carried out without the
            need to remove the adsorbent from its vessel. In contrast, granular activated
            carbon (GAC) which is used to adsorb high molecular weight, low volatility
            or strongly adsorbed species, must usually be removed from the adsorption
            vessel for regeneration in special furnaces. In this case the GAC needs to be
            heated to over 800~  Multiple hearth, rotary kiln, fluised bed and electric
            belt  furnaces  are  available  (Liu  and  Wagner  1985).  The  multiple  hearth
            furnace is shown in Figure 2.8. Further developments and examples of TSA
            are provided in Sections 7.4 and 7.5.
              A  practical  problem  in  thermal  swing processes  is  the  reduction  in  the
            capacity  or  life of the  adsorbent  when it is subjected  to repeated  thermal
            cycling. Another problem is the formation of coke in applications in which
            reactive  hydrocarbons  are  exposed  to  elevated  temperatures  during  the
            desorption/regeneration step.


            5.9    DISPLACEMENT FLUID

            Adsorbates can be removed from the adsorbent surface by replacing them
            with a more preferentially adsorbed species. This displacement fluid, which
            can be a gas, vapour or liquid, should adsorb about as strongly as the species
            which are to be desorbed. If the displacement fluid is adsorbed too strongly
            then there may be subsequent difficulties in removing it from the adsorbent.
            The  mechanism  for  desorption  of  the  original  adsorbate  involves  two
            aspects. First, the partial pressure of the original adsorbate in the gas phase
            surrounding the adsorbent is reduced (or the concentration is reduced in the
            case  of  a  liquid  displacement  fluid).  Secondly,  there  is  competitive
            adsorption  of the  displacement fluid. The  displacement  fluid is present  on
            the  adsorbent  at the next adsorption  step and thus it will contaminate  the
            product.  A  practical process therefore  requires that the displacement fluid
            must  be  recoverable  from  the  products  of the  adsorptive  separation  by  a
            process  such  as  simple  distillation.  This  is  the  basis  of  the  Sorbex  type
            process shown in Figure 5.13.
              One  advantage of the displacement fluid method  of regeneration  is that
            the  net heat generated  or consumed in the  adsorbent will be close to zero
            because the heat of adsorption of the displacement fluid is likely to be close
            to  that  of the  original  adsorbate.  Thus  the  temperature  of the  adsorbent
            should remain more or less constant throughout the cycle. In turn this leads
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