An investigation of the thermal and catalytic behaviour of potassium in biomass combustion

被引:164
作者
Jones, J. M. [1 ]
Darvell, L. I. [1 ]
Bridgeman, T. G. [1 ]
Pourkashanian, M. [1 ]
Williams, A. [1 ]
机构
[1] Univ Leeds, Sch Proc Environm & Mat Engn, Energy & Resources Res Inst, Leeds LS2 9JT, W Yorkshire, England
基金
英国工程与自然科学研究理事会;
关键词
biomass; potassium; catalysis; combustion;
D O I
10.1016/j.proci.2006.07.093
中图分类号
O414.1 [热力学];
学科分类号
摘要
Potassium, a key nutrient in biomass growth, contributes to problematic ash chemistry and corrosion in combustion. This study seeks to examine the behaviour and fate of potassium in biomass combustion under high temperature flame conditions. A model to predict potassium release is presented. Short rotation willow coppice was treated to reduce metals, by water-washing, and remove them, by demineralisation, and then potassium was doped into the demineralised sample. The resultant fuels have been studied for their combustion behaviours in methane-air flames, both as suspended, moving particles, and as stationary, supported particles, using high speed digital video. In the latter case, potassium release was measured simultaneously by emission spectroscopy. in both experiments, potassium was seen to catalyse devolatilisation, and for the stationary particles it was possible to detect potassium catalysis in the char burn-out rates. Demineralised willow was seen to melt in the flame and combustion resembled heavy oil combustion, rather than solid fuel combustion. The residual char was extremely slow to burn-out. In the potassium-doped particles, potassium was seen to evolve over three regimes, devolatilisation, char burn-out and, less significantly, during ash cooking. The first two evolution processes have been modelled using an apparent first order devolatilisation rate for the first stage, and a KOH evaporation model for the second stage. (c) 2006 The Combustion Institute. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1955 / 1963
页数:9
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