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Modeling and analysis of sampling artifacts in measurements of gas-particle partitioning of semivolatile organic contaminants using filter-sorbent samplers

机译:使用过滤吸附剂采样器对半挥发性有机污染物的气体颗粒分配进行测量时,采样伪影的建模和分析

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Measurements of gas/particle partition coefficients for semivolatile organic compounds (SVOCs) using filter-sorbent samplers can be biased if a fraction of gas-phase mass is measured erroneously as particle-phase due to sorption of SVOC gases to the filter, or, if a fraction of particle-phase mass is measured erroneously as gas-phase due to penetration of particles into the sorbent. A fundamental mechanistic model to characterize the air sampling process with filter-sorbent samplers for SVOCs was developed and partially validated. The potential sampling artifacts associated with measurements of gas-particle partitioning were examined for 19 SVOCs. Positive sampling bias (i.e., overestimation of gas/particle partition coefficients) was observed for almost all the SVOCs. For certain compounds, the measured partition coefficient was several orders of magnitude greater than the presumed value. It was found that the sampling artifacts can be ignored when the value of log[K-f/(K-p . C-p,C-a)] is less than 7. By normalizing the model, general factors that influence the sampling artifacts were investigated. Correlations were obtained between the dimensionless time required for the gas-phase SVOCs within the filter to reach steady state (T-s,T-s*) and the chemical V-p values, which can be used to estimate appropriate sampling time. The potential errors between measured and actual gas/particle partition coefficients of SVOCs as a function of sampling velocity and time were calculated and plotted for a range of SVOCs (vapor pressures: 10(-8) similar to 10(-3) Pa). These plots were useful in identifying bias from the sampling in previously-completed field measurements. Penetration of particles into the sorbent may result in significant underestimation of the partition coefficient for particles in the size range between 10 nm and 2 mu m. For most of the selected compounds, backup filters can be used to correct artifacts effectively. However, for some compounds with very low vapor pressure, the artifacts remained or became even larger than they were without the backup filter. Thus, the option of backup filters must be considered carefully in field measurements of the gas/particle partitioning of SVOCs. The results of this work will allow researchers to predict potential artifacts associated with SVOC gas/particle partitioning as functions of compounds, the concentration of particles, the distribution of particle sizes, sampling velocity, and sampling time. (C) 2015 Elsevier Ltd. All rights reserved.
机译:如果由于将SVOC气体吸附到过滤器上而将一部分气相质量错误地测量为颗粒相,则使用过滤器吸附剂采样器对半挥发性有机化合物(SVOC)的气体/颗粒分配系数的测量可能会产生偏差。由于颗粒渗透到吸附剂中,一部分颗粒相质量被错误地测量为气相。开发并部分验证了基本力学模型,该模型用SVOC的过滤吸附剂采样器表征了空气采样过程。针对19种SVOC,检查了与气体颗粒分配测量相关的潜在采样伪像。几乎所有SVOC都观察到正采样偏差(即,高估了气体/颗粒分配系数)。对于某些化合物,测得的分配系数比假定值大几个数量级。发现当log [K-f /(K-p。C-p,C-a)]的值小于7时,可以忽略采样伪像。通过对模型进行归一化,研究了影响采样伪像的一般因素。获得了过滤器内气相SVOC达到稳态(T-s,T-s *)所需的无量纲时间与化学V-p值之间的相关性,可将其用于估算适当的采样时间。计算了SVOC的实测气体/颗粒分配系数与实际气体/颗粒分配系数之间的潜在误差,该误差是采样速度和时间的函数,并针对一定范围的SVOC(蒸气压:10(-8)类似于10(-3)Pa)作图。这些图可用于在先前完成的现场测量中从采样中识别偏差。颗粒渗透到吸附剂中可能会导致低估10纳米至2微米尺寸范围内颗粒的分配系数。对于大多数选定的化合物,备用过滤器可用于有效地校正伪影。但是,对于某些蒸气压非常低的化合物,与没有备用过滤器的情况相比,伪像仍保持或变得更大。因此,在现场测量SVOC的气体/颗粒分配时,必须仔细考虑备用过滤器的选择。这项工作的结果将使研究人员能够预测与SVOC气体/颗粒分配相关的潜在伪像,这些化合物是化合物的功能,颗粒浓度,粒径分布,采样速度和采样时间的函数。 (C)2015 Elsevier Ltd.保留所有权利。

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