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High-temperature aerosol formation in wood pellets flames: Spatially resolved measurements

机译:木屑颗粒火焰中高温气溶胶的形成:空间分辨的测量

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The formation and evolution of high-temperature aerosols during fixed bed combustion of wood pellets in a realistic combustion environment were investigated through spatially resolved experiments. The purpose of this work was to investigate the various stages of aerosol formation from the hot flame zone to the flue gas channel. The investigation is important both for elucidation of the formation mechanisms and as a basis for development and validation of particle formation models that can be used for design optimization. Experiments were conducted in an 8-kW-updraft fired-wood-pellets combustor. Particle samples were withdrawn from the centerline of the combustor through 10 sampling ports by a rapid dilution sampling probe. The corresponding temperatures at the sampling positions were in the range 200-1450 ℃. The particle sample was size-segregated in a low-pressure impactor, allowing physical and chemical resolution of the fine particles. The chemical composition of the particles was investigated by SEM/EDS and XRD analysis. Furthermore, the experimental results were compared to theoretical models for aerosol formation processes. The experimental data show that the particle size distribution has two peaks, both of which are below an aerodynamic diameter of 2.5 μm (PM_(2.5)). The mode diameters of the fine and coarse modes in the PM_(2.5) region were ~0.1 and ~0.8 μm, respectively. The shape of the particle size distribution function continuously changes with position in the reactor due to several mechanisms. Early, in the flame zone, both the fine mode and the coarse mode in the PM_(2.5) region were dominated by particles from incomplete combustion, indicated by a significant amount of carbon in the particles. The particle concentrations of both the fine and the coarse mode decrease rapidly in the hot oxygen-rich flame due to oxidation of the carbon-rich particles. After the hot flame, the fine mode concentration and particle diameter increase gradually when the temperature of the flue gas drops. The main contribution to this comes from condensation on preexisting particles in the gas of alkali sulfates, alkali chlorides, and Zn species formed from constituents vaporized in the fuel bed. The alkali sulfates were found to condense at a temperature of ~950℃ and alkali chlorides condensed later at ~600 ℃. This agrees well with results of chemical equilibrium calculation of the gas-to-particle conversion temperature. After the hot flame the coarse mode concentration decreased very little when the flue gas was cooled. In addition to carbon, the coarse mode consists of refractory metals and also considerable amounts of alkali.
机译:通过空间分辨实验研究了木质颗粒在固定燃烧条件下固定床燃烧过程中高温气溶胶的形成和演化。这项工作的目的是研究从热火焰区到烟气通道的气溶胶形成的各个阶段。该研究对于阐明形成机理以及作为开发和验证可用于设计优化的颗粒形成模型的基础都是重要的。实验是在8千瓦以上的燃木颗粒燃烧器中进行的。通过快速稀释采样探针通过10个采样口从燃烧室的中心线抽取颗粒样品。采样位置的相应温度在200-1450℃范围内。将颗粒样品在低压撞击器中进行尺寸分离,从而可以对细颗粒进行物理和化学拆分。通过SEM / EDS和XRD分析研究了颗粒的化学组成。此外,将实验结果与气雾形成过程的理论模型进行了比较。实验数据表明,粒径分布有两个峰,两个峰均在空气动力学直径2.5μm(PM_(2.5))以下。 PM_(2.5)区的细模和粗模的模直径分别为〜0.1和〜0.8μm。由于多种机理,粒度分布函数的形状随反应器中位置的变化而连续变化。早期,在火焰区域,PM_(2.5)区域中的精细模式和粗糙模式均以不完全燃烧产生的颗粒为主,这表明颗粒中存在大量碳。由于富碳颗粒的氧化,在富氧热火焰中细模式和粗模式的颗粒浓度都迅速降低。在热火焰之后,当烟气温度下降时,精细模式浓度和粒径逐渐增加。对此的主要贡献来自在碱金属硫酸盐,碱金属氯化物和由在燃料床中蒸发的成分形成的Zn物种的气体中预先存在的颗粒上的冷凝。发现碱金属硫酸盐在〜950℃的温度下冷凝,而碱金属氯化物在〜600℃的温度下冷凝。这与气体-颗粒转化温度的化学平衡计算的结果非常吻合。在热火焰之后,当烟气冷却时,粗模式浓度几乎没有降低。除碳外,粗模式还包含难熔金属和大量碱。

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