Abstract

Infrared laser absorption spectroscopy (IRLAS) and laser-induced fluorescence spectroscopy (LIF) are applied in the present study for online in-situ characterization of volatiles products in the close vicinity of a single pyrolysing wood sphere. These advanced analytical techniques are combined with online measurements of temperature and mass evolutions in order to gain further insight into the complex processes occurring during slow pyrolysis of thermally thick wood particles. Three different heating rates (5, 10, 20°C/min) and two wood types (beech, pine) were used. Time-resolved absolute concentrations of the main permanent gases CO2, CO, CH4 and H2O were measured applying IRLAS. From the LIF measurements the qualitative temporal release of polycyclic aromatic hydrocarbons (PAHs) could be deduced. Different behaviors regarding the release of volatiles, temperature evolution and conversion rates were observed for both wood species, which could not be ascribed only to the different content of cellulose, hemicellulose and lignin. According to the measured volatiles evolution an enhancement of heterogeneous catalytic tar cracking seemed to be present with higher heating rates for both wood types. However, the evolution of exothermicity and PAH release differed for both wood types indicating different reaction pathways. An analysis of possible reaction pathways including secondary reactions is performed taking into account all experimental findings about the in-situ composition of the volatiles and the evolution of the PAHs as well as the exothermicity. The differences in the pyrolytic behavior of both species can be related to both the chemical and physical properties of the raw materials.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.