Abstract

Palmitic acid (C16:0) and stearic acid (C18:0) are among the most abundant products in cooking emission, and thus could serve as potential molecular tracers in estimating the contributions of cooking emission to particulate matter (PM2.5) pollution in the atmosphere. Organic tracer analysis in filter-based samples generally involves extraction by organic solvents, followed by filtration. In these procedures, disposable plastic labware is commonly used due to convenience and as a precaution against sample-to-sample cross contamination. However, we observed contamination for both C16:0 and C18:0 fatty acids, their levels reaching 6–8 ppm in method blanks and leading to their detection in 9% and 42% of PM2.5 samples from Hong Kong, indistinguishable from the blank. We present in this work the identification of plastic syringe and plastic syringe filter disc as the contamination sources. We further demonstrated that a new method procedure using glass syringe and stainless-steel syringe filter holder offers a successful solution. The new method has reduced the contamination level from 6.6 ± 1.2 to 2.6 ± 0.9 ppm for C16:0 and from 8.9 ± 2.1 to 1.9 ± 0.8 ppm for C18:0 fatty acid. Consequently, the limit of detection (LOD) for C16:0 has decreased by 57% from 1.8 to 0.8 ppm and 56% for C18:0 fatty acid from 3.2 to 1.4 ppm. Reductions in both LOD and blank variability has allowed the increase in quantification rate of the two fatty acids in ambient samples and thereby retrieving more data for estimating the contribution of cooking emission to ambient PM2.5. With the assistance of three cooking related tracers, palmitic acid (C16:0), stearic acid (C18:0) and cholesterol, positive matrix factorization analysis of a dataset of PM2.5 samples collected from urban Hong Kong resolved a cooking emission source. The results indicate that cooking was a significant local PM2.5 source, contributing to an average of 2.2 µgC/m3 (19%) to organic carbon at a busy downtown roadside location and 1.8 µgC/m3 (15%) at a general urban site.

Highlights

  • Palmitic acid (C16:0) and stearic acid (C18:0) are among the most abundant particulates in cooking emission

  • They can be released or formed by hydrolysis or through thermal oxidation during heating [1,2]. Since they are ubiquitous in plants and animal fats, they were found in all cooking emission particulate matter (PM), with compositions mirroring that of cooking oil or meat kind [3]

  • Method blanks and field blanks went through all the procedures shown in Figure 1, while instrument blanks preparation started from nitrogen blow-drying onwards, after spiking internal standard d31-palmitic acid

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Summary

Introduction

Palmitic acid (C16:0) and stearic acid (C18:0) are among the most abundant particulates in cooking emission. They exist in the form of triglycerides, phospholipids, or free fatty acids in oil or meat. They can be released or formed by hydrolysis or through thermal oxidation during heating [1,2]. Since they are ubiquitous in plants and animal fats, they were found in all cooking emission particulate matter (PM), with compositions mirroring that of cooking oil or meat kind [3]. A more recent air quality campaign in Beijing deployed more advanced instrumentation such as an Aerodyne High-Resolution Time-of-Flight

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