Page 189 - Biomass Gasification, Pyrolysis And Torrefaction Practical Design and Theory
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166                          Biomass Gasification, Pyrolysis and Torrefaction



              TABLE 5.4 Kinetic Rate Constants for One-Step Single-Reaction
              Global Model
                                                     21
              Fuel       Temperature (K)  E (kJ/mol)  A (s )  References
              Cellulose  520 1270      166.4      3.9 3 10 11  Lewellen et al. (1977)
              Hemicellulose 520 1270   123.7      1.45 3 10 9  Min (1977)
              Lignin     520 1270      141.3      1.2 3 10 8  Min (1977)
              Wood       321 720       125.4      1.0 3 10 8  Nolan et al. (1973)
              Almond shell  730 880    95 121     1.8 3 10 6  Font et al. (1990)
              Beech      450 700       84 (T . 600K) 2.3 3 10 4  Barooah and Long
              sawdust                                      (1976)





               Solving this equation we get:
                                    X 5 1   A expð2ktÞ                 (5.5)
            where A is the preexponential coefficient, k 5 E/RT E is the activation energy
            (J/mol), R is the gas constant (J/mol K), and T is the temperature (K).
               Owing to the difficulties in extracting data from dynamic thermogravimetric
            analysis, reliable data on the preexponential factor, A, and the activation
            energy, E, are not easily available for fast pyrolysis (Reed, 2002, p. II-103).
            However, for slow heating, we can obtain some reasonable values. If the effect
            of secondary cracking and the heat-transfer limitation can be restricted, the
            weight-loss rate of pure cellulose during pyrolysis can be represented by an
            irreversible, one-stage global first-order equation.
               For the one-step global reaction model, Table 5.4 lists values of the acti-
            vation energy E and the preexponential factor A, for the pyrolysis of various
            biomass types at a relatively slow heating rate.
               Other models are not discussed here, but details are available in several
            publications, including Blasi (1993).


            5.5 HEAT TRANSFER IN A PYROLYZER
            The preceding discussions assume that the heat or mass transport rate is too
            high to offer any resistance to the overall rate of pyrolysis. This is true at a
            temperature of 300 400 C (Thurner and Mann, 1981), but at higher tem-

            peratures heat and mass transport influence the overall rate and so cannot be
            neglected. This section deals with heat transport during pyrolysis.
               During pyrolysis, heat is transported to the particle’s outer surface by
            radiation and convection. Thereafter, it is transferred to the interior of the
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