Distribution of temperature, H2 O and atomic potassium during entrained flow biomass combustion: Coupling in situ TDLAS with modeling approaches and ash chemistry Show others and affiliations
2018 (English) In: Combustion and Flame, ISSN 0010-2180, E-ISSN 1556-2921, Vol. 188, p. 488-497Article in journal (Refereed) Published
Abstract [en]
Tunable diode laser absorption spectroscopy (TDLAS) is employed for simultaneous detection of gas temperature, water vapor (H2 O) and gas-phase atomic potassium, K(g), in an atmospheric, research-scale entrained flow reactor (EFR). In situ measurements are conducted at four different locations in the EFR core to study the progress of thermochemical conversion of softwood and Miscanthus powders with focus on the primary potassium reactions. In an initial validation step during propane flame operation, the measured axial EFR profiles of H2 O density-weighted, path-averaged temperature, path-averaged H2 O concentration and H2 O column density are found in good agreement with 2D CFD simulations and standard flue gas analysis. During biomass conversion, temperature and H2 O are significantly higher than for the propane flame, up to 1500 K and 9%, respectively, and K(g) concentrations between 0.2 and 270 ppbv are observed. Despite the large difference in initial potassium content between the fuels, the K(g) concentrations obtained at each EFR location are comparable, which highlights the importance of considering all major ash-forming elements in the fuel matrix. For both fuels, temperature and K(g) decrease with residence time, and in the lower part of the EFR, K(g) is in excellent agreement with thermodynamic equilibrium calculations evaluated at the TDLAS-measured temperatures and H2 O concentrations. However, in the upper part of the EFR, where the measured H2 O suggested a global equivalence ratio smaller than unity, K(g) is far below the predicted equilibrium values. This indicates that, in contrast to the organic compounds, potassium species rapidly undergo primary ash transformation reactions even if the fuel particles reside in an oxygen-deficient environment
Place, publisher, year, edition, pages Elsevier, 2018. Vol. 188, p. 488-497
National Category
Energy Engineering
Research subject Energy Engineering
Identifiers URN: urn:nbn:se:ltu:diva-66385 DOI: 10.1016/j.combustflame.2017.10.013 ISI: 000424859100040 Scopus ID: 2-s2.0-85032255301 OAI: oai:DiVA.org:ltu-66385 DiVA, id: diva2:1154872
Note Validerad;2017;Nivå 2;2017-11-06 (andbra)
2017-11-062017-11-062018-03-02 Bibliographically approved