The effects of oxygen concentration and gas temperature on coal stream ignition and particle surface temperature in reducing-to-oxidizing environments

被引:1
作者
Khatri, Dishant [1 ]
Yang, Zhiwei [1 ]
Axelbaum, Richard L. [1 ]
机构
[1] Washington Univ, Consortium Clean Coal Utilizat, Dept Energy Environm & Chem Engn, St Louis, MO 63130 USA
基金
美国国家科学基金会;
关键词
Coal combustion; Reducing environment; Two-color pyrometry; Coal ignition; Surface temperature; CHEMILUMINESCENCE; COMBUSTION;
D O I
10.1016/j.proci.2020.06.185
中图分类号
O414.1 [热力学];
学科分类号
摘要
In the near-burner region of pulverized coal burners, two zones exist, with very different oxygen concentrations. The first zone is a locally reducing environment, caused by the fast release of volatiles from a region of dense coal particles, and the second zone, which is surrounding the first zone, is a hot oxidizing environment. The transition of coal particles from the reducing zone to the oxidizing zone affects early stage coal combustion characteristics, such as devolatilization, ignition and particle temperature history. In this work, we used a two-stage Hencken flat-flame burner to simulate the conditions that coal particles experience in practical combustors when they transition from a reducing environment to an oxidizing environments. The composition of the reducing environment was chosen to approximate that of a typical coal volatile. Three oxygen concentrations (5, 10 and 15 vol%) in the "ambient" oxidizing environment were tested, corresponding to those at different distances downstream from a commercial burner. The corresponding gas temperatures for the oxidizing environments were adjusted for the different oxygen concentrations such that the "volatile" flame temperatures were the same, as this is what would be expected in a commercial combustor. High speed videography was used to obtain the ignition characteristics, and RGB color pyrometry was used to measure particle surface temperatures. Two different sizes of coal particles were used. It is found that when particles undergo a reducing-to-oxidizing transition at high temperatures, the particles are preheated such that the critical factor for ignition delay is point at which the particle is in the presence of oxygen, not the concentration of oxygen. The ignition delay of large particles is found to be 53% longer than that of small particles due to their higher thermal mass and slower devolatilization. The oxygen concentration in the ambient have a negligible effect on early-stage particle temperatures. (c) 2020 Published by Elsevier Inc. on behalf of The Combustion Institute.
引用
收藏
页码:4073 / 4081
页数:9
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