Page 57 - Adsorbents - fundamentals and applications
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42   SORBENT SELECTION: CRITERIA

                     Eq. 3.1, is followed by both components. For a binary mixture, the extended
                     Langmuir equation, Eq. 3.4., is

                                                        b
                                                     q m i i P i
                                             q i =                                 (3.58)
                                                  1 + b 1 P 1 + b 2 P 2
                       The first factor in the PSA parameter is the equilibrium selectivity (α 1,2 )and
                     is defined as follows:
                                                      x 1  y 2
                                                α 1,2 =  ·                         (3.59)
                                                      x 2  y 1
                     where x 1 , x 2 are the mole fractions of the two components on the adsorbent
                     surface, whereas y 1 , y 2 are the corresponding mole fractions in the gas phase. It
                     will be assumed that component (1) is the more strongly adsorbed species. Using
                     the extended Langmuir equation in conjunction with the definition given above
                     (Eq. 3.59), it can be shown that the adsorbent selectivity for component (1) is a
                     constant for the entire range of partial pressures as follows:

                                                      b
                                                   q m 1 1     K 1
                                             α 1,2 =      =                        (3.60)
                                                      b
                                                   q m 2 2  K 2
                     The product (q mi b i ) corresponds to the initial slope of the isotherm, or Henry’s
                     constant (K), for component i. Hence, the adsorbent selectivity is equivalent to
                     the ratio of the initial slopes of the isotherms of the two components, or K 1 /K 2 .
                     It should be noted that the selectivity has resulted in a constant value simply
                     because of the nature of the Langmuir isotherm. If, however, a different model
                     such as the loading ratio correlation (Eq. 3.5) is used, the selectivity is likely to
                     be dependent on the operating pressures of the PSA cycle.
                       Another important factor for PSA separations is the change in the adsorbed
                     amounts of the two components upon cycling the pressure. The working capacity
                     of a sorbent typically refers to the strongly adsorbed species and is defined as
                     the difference between the adsorbed amounts at the adsorption (high) pressure
                     and the desorption (low) pressure. Strictly speaking, the working capacity should
                     be defined with respect to the adsorbed amounts under the mixture conditions
                     (that is, using a binary component isotherm). However, using a pure component
                     isotherm can suffice to make the calculation of the parameter facile. A ratio
                     of the working capacities of the two components would give an idea about the
                     adsorption performance for a particular pressure swing cycle. Hence, the second
                     factor to the parameter is the working capacity selectivity ratio and is defined as:


                                                        q 1
                                                  W =                              (3.61)
                                                        q 2
                       Having defined the two contributing factors to the parameter, the PSA sorbent
                     selection parameter (S) can be written as follows:

                                                 S = W · a 1,2                     (3.62)
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