In this study, the kinetics of fast pyrolysis of pine wood biomass at short timescales is evaluated using analytical Curie-point and Pyroprobe® pyrolyzers. Curie-point pyrolysis was highly effective in ensuring that the biomass was heated to the set temperatures at very high heating rates and precise time scales. This is the first time the mass loss data of lignocellulosic biomass using a Curie-point pyrolyzer is being reported at short timescales of the order of 10−1 s. COMSOL Multiphysics® simulations, employed to determine the time required for the sample to heat-up to the final reaction temperature, proved that it was 0.2 s in the Curie-point pyrolyzer and 6–8 s in the Pyroprobe® reactor. Within a time period of 0.5 s for temperatures greater than 400 °C, complete conversion of the biomass was achieved using a Curie-point pyrolyzer. The conventional reaction kinetic models were not able to explain the pyrolysis behavior of the sample in a Curie-point pyrolyzer, especially at short timescales of 0–0.5 s. However, the kinetics until 0.4 s, corresponding to the release of light volatiles, is shown to follow the sigmoidal Avrami model, while the major devolatilization stage in the range of 0.4–0.5 s could not be described by a standard kinetic model. This showed that the reactions at short time scales are highly complex processes governed by the competing decomposition rates of the biomolecules. The isothermal mass loss experiments using the Pyroprobe® showed that pyrolysis followed first-order kinetics, and the rate of decomposition was slower as it took 10–20 s for the conversion to attain a steady value. The kinetic compensation for the pyrolysis of pinewood was constructed using the fast pyrolysis data and the kinetics of slow pyrolysis using isoconversional models, and it was found to be ln(A) = 0.18*Ea – 3.12.
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