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118   ACTIVATED CARBON

                                          2
                                       D/r = 3.37 × 10 −3  3 −1
                                 1.0                      3.36 × 10 −4

                                 0.8                       2.64 × 10 −4


                                 0.6
                               M t /M ∞

                                 0.4
                                                          2.86 × 10 −5

                                 0.2
                                                Methane   Nitrogen
                                                Oxygen    Argon
                                                Equation
                                 0.0
                                    0      200     400     600      800    1000
                                                     Time (s)
                     Figure 5.27. Uptake rates of (from top down) O 2 ,Ar, N 2 ,and CH 4 in Takeda 3A CMS at
                                                                                      −4
                                                  2
                                                                            −3
                     303 K (Ma et al., 1991). The values of D/r (in 1/s) are, respectively, 3.37 × 10 ,3.36 × 10 ,
                                        −5
                            −4
                     2.64 × 10 ,and 2.86 × 10 .
                     controlled pyrolysis of thermosetting polymeric membranes. These membranes
                     have been prepared by either directly pyrolyzing hollow-fiber polymeric materi-
                     als or pyrolizing a thin layer of polymer coated on a macroporous support. Both
                     sintered stainless steel tubing and macroporous alumina tubing have been used as
                     the support. Compared with traditional polymeric membranes for gas separation
                     (Paul and Yampol’skii, 1994), the CMS membranes showed both superior sepa-
                     ration properties (i.e., permeances and selectivity) and higher stability (Jones and
                     Koros, 1994a). The higher stability (i.e., greater resistance to solvents, chemical
                     attack, and heat) offers the advantage of operating in environments prohibitive
                     to polymeric membranes.
                       The earliest report on CMS membranes obtained from hollow fiber polymeric
                     membranes appears to be from Koresh and Soffer (1983) and Soffer et al. (1987).
                     By comparing CMS membranes derived from different polymeric membranes,
                     Jones and Koros (1994a) found that the ones from aromatic polyimides yielded
                     the best separation and mechanical properties. The polymers tested by Jones and
                     Koros were cellulose acetate, polyaramides, and polyimides. Polyfurfural alcohol
                     was used by Foley and co-workers (Foley, 1995; Shiflett and Foley, 1999; Strano
                     and Foley, 2002). A comparison of the O 2 permeances and O 2 /N 2 selectivities
                     showed that the CMS membrane from polyimide was indeed much better than
                     that from polyfurfural alcohol, as will be seen shortly.
                       The quality of the CMS membrane is determined not only by the type of
                     the polymer precursor, but also by the pyrolysis protocols (Jones and Koros,
                     1994a) as well as the manner that the polymer film is deposited on the support
                     (Shiflett and Foley, 1999). The pyrolysis protocol includes temperature program
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