Abstract

Particle-into-Liquid Samplers (PILS) have become a standard aerosol collection technique, and are widely used in both ground and aircraft measurements in conjunction with off-line ion chromatography (IC) measurements. Accurate and precise background samples are essential to account for gas-phase components not efficiently removed and any interference in the instrument lines, collection vials or off-line analysis procedures. For aircraft sampling with PILS, backgrounds are typically taken with in-line filters to remove particles prior to sample collection once or twice per flight with more numerous backgrounds taken on the ground. Here, we use data collected during the Front Range Air Pollution and Photochemistry Éxperiment (FRAPPÉ) to demonstrate that not only are multiple background filter samples are essential to attain a representative background, but that the chemical background signals do not follow the Gaussian statistics typically assumed. Instead, the background signals for all chemical components analyzed from 137 background samples (taken from ∼78 total sampling hours over 18 flights) follow a log-normal distribution, meaning that the typical approaches of averaging background samples and/or assuming a Gaussian distribution cause an over-estimation of background samples – and thus an underestimation of sample concentrations. Our approach of deriving backgrounds from the peak of the log-normal distribution results in detection limits of 0.25, 0.32, 3.9, 0.17, 0.75 and 0.57 μg m−3 for sub-micron aerosol nitrate (NO3−), nitrite (NO2−), ammonium (NH4+), sulfate (SO42−), potassium (K+) and calcium (Ca2+), respectively. The difference in backgrounds calculated from assuming a Gaussian distribution versus a log-normal distribution were most extreme for NH4+, resulting in a background that was 1.58× that determined from fitting a log-normal distribution.

Highlights

  • The composition of atmospheric aerosols is the result of primary emissions, secondary aerosol formation, and atmospheric aging chemistry

  • We suggest an approach of fitting the distribution of background sample concentrations to a lognormal distribution in order to find the mode, which more accurately represents the background concentration

  • We focus on eight inorganic ions: ClÀ, NO2À, NO3À, SO42À, NH4þ, Kþ, Mg2þ, and Ca2þ

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Summary

Introduction

The composition of atmospheric aerosols is the result of primary emissions, secondary aerosol formation, and atmospheric aging chemistry. One method for characterizing bulk aerosol composition is collection of aerosols into the aqueous-phase using a Particle-into-Liquid Sampler (PILS). These systems have been used extensively over the last decade in both aircraft and ground based studies, and have been used to. Histograms of background distributions can be fit to lognormal distributions for accurate background determination This procedure leads to substantially lower calculated limits of detection for ammonium and other inorganic ions. Particle-into-Liquid Samplers (PILS) have become a standard aerosol collection technique, and are widely used in both ground and aircraft measurements in conjunction with off-line ion chromatography (IC) measurements. The difference in backgrounds calculated from assuming a Gaussian distribution versus a log-normal distribution were most extreme for NH4þ, resulting in a background that was 1.58Â that determined from fitting a log-normal distribution

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