烟囱排放浓度测量的不确定性建模

S. Knotek, J. Geršl
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引用次数: 0

摘要

本文描述了垂直烟囱中工业排放的测量不确定度及其对不同几何结构和物理条件的依赖性的研究。由于工业过程排放限值的立法要求正在减少,更高的测量精度变得越来越重要,需要实施新的不确定度标准。这项贡献是欧洲计量创新与研究计划(EMPIR)下的研究项目18NRM04 Heroes的一部分。采用CFD模型分析了三种不同形状的供水管、不同尺寸的颗粒和不同浓度的堆内颗粒分布。考虑圆截面直径为0.75 m的垂直烟囱,供水管不含弯管、一弯管或两弯管。进入堆积的颗粒数决定了初始体积浓度为0.1 ~ 10 mg·m -3,粒径为10 ~ 50 μm。比较了几个截面上的浓度场,并分析了粒子分布随物理条件和所选择的堆的几何形状的变化。结果表明,浓度曲线对初始浓度的敏感性不高。另一方面,当堆的几何形状或颗粒直径发生变化时,浓度场发生了显著的变化。在等动力学取样实践中,总浓度是从几个点的测量中计算出来的,应考虑到这一点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modelling of uncertainties of an emission concentration measurement in stacks
This contribution describes a research of measurement uncertainty of industrial emissions flowing through vertical stacks and its dependence on different geometrical configurations and physical conditions. Since the legislative requirements for emission limits from industrial processes are decreasing, the higher measurement accuracy is becoming more important and new uncertainty standards needs to be implemented. This contribution is a part of the research project 18NRM04 Heroes under European Metrology Program for Innovation and Research (EMPIR). CFD modelling is used to analyse particle distributions in stacks with three different geometries of a supply pipe, different size of the particles and several concentrations. Vertical stack with a circular cross section of a diameter of 0.75 m is considered with the supply pipe containing none, one or two bends. The number of particles entering the stack defines the initial volumetric concentration from 0.1 to 10 mg·m -3 with the particle size from 10 to 50 μm. Concentration fields in several cross-sections were compared and the particle distributions were analysed as functions of the physical conditions and the chosen geometry of the stack. The results show not very high sensitivity of the concentration profiles on the initial concentrations. On the other hand, significant changes of the concentration fields are observed when the stack geometry or the particle diameter is changed. This should be taken into account in the iso-kinetic sampling practise where the overall concentrations are calculated from measurements in several points.
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