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Using a new inversion matrix for a fast-sizing spectrometer and a photo-acoustic instrument to determine suspended particulate mass over a transient cycle for light-duty vehicles

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posted on 2016-09-22, 20:18 authored by Jian Xue, Yang Li, David Quiros, Xiaoliang Wang, Thomas D. Durbin, Kent C. Johnson, Georgios Karavalakis, Shaohua Hu, Tao Huai, Alberto Ayala, Heejung S. Jung

Integrated particle size distribution (IPSD) is a promising alternative method for estimating particulate matter (PM) emissions at low levels. However, a recent light-duty vehicle (LDV) emissions study showed that particle mass estimated using IPSD (MIPSD) with the TSI Engine Exhaust Particle Sizer (EEPS) Default Matrix was 56–75% lower than mass derived using the reference gravimetric method (MGrav) over the Federal Test Procedure (FTP). In this study, MIPSD calculated with a new inversion matrix, the Soot Matrix, is compared with MGrav and also photoacoustic soot mass (MSoot), to evaluate potential improvement of the IPSD method for estimating PM mass emissions from LDVs. In addition, an aerodynamic particle sizer (APS) was used to estimate mass emission rates attributed to larger particles (0.54–2.5 µm in aerodynamic diameter) that are not measured by the EEPS. Based on testing of 10 light-duty vehicles over the FTP cycle, the Soot Matrix significantly improved agreement between MIPSD and MGrav by increasing slopes of MIPSD/MGrav from 0.45–0.57 to 0.76–1.01 for gasoline direct injected (GDI) vehicles; however, for port-fuel injection (PFI) gasoline vehicles, a significant discrepancy still existed between MIPSD and MGrav, with MIPSD accounting for 34 ± 37% of MGrav. For all vehicles, strong correlations between MIPSD and MSoot were obtained, indicating the IPSD method is capable of capturing mass of soot particles. The discrepancy between the MIPSD and MGrav for PFI vehicles, which have relatively low PM emissions (0.22 to 1.83 mg/mile), could be partially due to limited size range of the EEPS by not capturing larger particles (0.54–2.5 µm) that accounts for ∼0.08 mg/mile of PM emission, uncertainties of particle effective density, and/or gas-phase adsorption onto filters that is not detected by in situ aerosol instrumentation.

Copyright © 2016 American Association for Aerosol Research

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