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Remediation and Control Technologies
Emissions During and Real-world Frequency of Heavy-duty Diesel Particulate Filter Regeneration Chris Ruehl, Jeremy D. Smith, Yilin Ma, Jennifer Erin Shields, Mark Burnitzki, Wayne Sobieralski, Robert Ianni, Donald J. Chernich, M.-C. Oliver Chang, John Francis Collins, Seungju Yoon, David Quiros, Shaohua Hu, and Harry Dwyer Environ. Sci. Technol., Just Accepted Manuscript • DOI: 10.1021/acs.est.7b05633 • Publication Date (Web): 19 Apr 2018 Downloaded from http://pubs.acs.org on April 19, 2018
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Environmental Science & Technology
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Emissions during and Real-world Frequency of
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Heavy-duty Diesel Particulate Filter Regeneration
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Chris Ruehl*, Jeremy D. Smith, Yilin Ma, Jennifer Erin Shields, Mark Burnitzki, Wayne
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Sobieralski, Robert Ianni, Donald J. Chernich, M.-C. Oliver Chang, John Francis Collins,
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Seungju Yoon, David Quiros, Shaohua Hu & Harry Dwyer
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California Air Resources Board
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1001 I St.
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Sacramento, CA 95812
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ABSTRACT: Recent tightening of particulate matter (PM) emission standards for heavy-duty
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engines has spurred the widespread adoption of diesel particulate filters (DPF), which need to be
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regenerated periodically to remove trapped PM. The total impact of DPFs therefore depends not
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only on their filtering efficiency during normal operation, but also on the emissions during and
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the frequency of regeneration events. We performed active (parked and driving) and passive
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regenerations on two heavy-duty diesel vehicles (HDDVs), and report the chemical composition
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of emissions during these events, as well as the efficiency with which trapped PM is converted to
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gas-phase products. We also collected activity data from 85 HDDVs to determine how often
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regeneration occurs during real-world operation. PM emitted during regeneration ranged from
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0.2 to 16.3 g, and the average time and distance between real-world active regenerations was
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28.0 hours and 599 miles. These results indicate that regeneration of real-world DPFs does not
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substantially offset the reduction of PM by DPFs during normal operation. The broad ranges of
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regeneration frequency per truck (3 – 100 hours and 23 – 4078 miles) underscore the challenges
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in designing engines and associated aftertreatment that reduce emissions for all real-world duty
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cycles.
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INTRODUCTION
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Heavy-Duty Vehicles (HDVs) used 18% of all transportation energy in the United States in
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2012, and this contribution is projected to grow to 28% by 2040.1,2 Although Phase 2 U.S. EPA
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standards for medium- and heavy-duty vehicles emissions project that their energy use will
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decrease 22% by 2040 relative to 2016 (Phase 1) standards, diesel consumption is projected to
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decrease by only 18%.1 It is all but certain that HDVs will remain a major contributor of diesel
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combustion emissions over the coming decades.
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Many diesel emissions (or the secondary products formed when they react after emission) have
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been linked to adverse human health effects. These include gas-phase pollutants such as ozone
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and NOx. Ambient particulate matter (PM) concentrations, however, have consistently shown the
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highest correlations with human health endpoints.3-5 Other diesel-specific epidemiological work
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has implicated PM from this source as a cause of disease, typically lung cancer.6,7 As a result of
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this and much other work, diesel PM has been declared a toxic air contaminant by the State of
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California,8 and diesel exhaust a carcinogen by the International Agency of Research on Cancer.9
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In response to human health concerns, PM emissions standards for heavy-duty engines in the
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United States have been tightened considerably, from 600 to 10 mg/bhp-hr between 1987 and
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2007. Current standards effectively require the use of diesel particulate filters (DPFs) to trap PM
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emitted by heavy-duty engines. Under normal operation, DPFs remove more than 95% of
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engine-out PM, allowing such low standards to be met,10 but PM trapped in the DPF needs to be
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removed periodically before it impedes the exhaust flow. Emissions associated with this
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“regeneration” of the filter may strongly impact total HDDV emissions. While certification of
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the associated engines takes into account both the frequency of and the emissions associated with
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DPF regeneration during engine dynamometer testing, much less work has been done to
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characterize these variables in real-world operation. Furthermore, work is needed to characterize
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the efficiency with which the regeneration process converts trapped carbonaceous PM into CO2
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and other gases, and to characterize the chemical composition of regeneration emissions.
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Regeneration involves heating the DPF to a high enough temperature that trapped PM
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(primarily soot) is oxidized. These regenerations can occur either while the HDDV is parked or
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while it is driving, and on-road regenerations can either be active, involving injection of fuel into
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the HDDV aftertreatment, or passive, relying on the heat associated with normal engine
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operation. It is not known, however, how the concentration and composition of emissions depend
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on the type of regeneration. To address this question, we performed active parked, passive road,
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and active road DPF regenerations for both a 2007 (w/DPF) and 2010 (w/DPF and Selective
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Catalytic Reduction, or SCR) engine model year (MY) HDDV.
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Active regeneration of the DPFs on these two HDDVs was examined previously,11-13 and the
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size distribution and total mass of the emitted PM was reported. These regenerations were
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characterized by two phases: an initial “soot combustion” phase that featured a wide range of
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particle diameters, some larger than 1 µm, and a subsequent “fuel combustion” regime that was
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dominated by smaller particle with diameters ~ 30 nm. This previous work did not determine the
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composition of these emissions, however, and also did not quantify the mass lost from the DPF
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during regeneration. This study extends the previous work that only evaluated emissions during
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parked active DPF regenerations to also include driving regenerations (both active and passive)
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at vehicle speeds ~50 mph.
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This work reports the composition of emissions during parked, active driving, and passive
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driving DPF regenerations. We compare these emissions to the gravimetrically quantified PM
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lost from the DPF during regeneration. Finally, we report the real-world frequency of DPF
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regenerations from 85 HDDVs used in ten different vocations that are representative of on-road
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HDDV activity in the State of California.14 These results are used in combination with the
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dynamometer tests described above to estimate the real-world impact of DPF regenerations.
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MATERIALS AND METHODS
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Two Class 8 Heavy-Duty Diesel Vehicles (HDDVs), one with a MY 2007 engine including an
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original equipment manufacturer (OEM) DPF and the other with a MY 2010 engine including
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an OEM DPF and (downstream of the DPF) an SCR to remove NOx, were tested on a heavy-duty
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chassis dynamometer (Burke E Porter) at the California Air Resources Board’s Depot Park
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Facility, located in Sacramento, CA. The aftertreatment systems on both HDDVs included a
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diesel oxidation catalyst. The test fuel was Ultra Low Sulfur Diesel (ULSD), with a maximum
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sulfur content of 15 ppm. HDDV properties are summarized in Table S1. Details on both the
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DPF loading procedure and the DPF regenerations, both of which were conducted on the
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dynamometer, can be found in the SI.
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The instrumentation used to measure real-time emissions, as well as analyses conducted on PM
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collected on filters, are also described in the SI. Briefly, we performed chemical analysis of both
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gas-phase and particulate tailpipe emissions during active parked, active driving, and passive
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driving DPF regenerations. We also gravimetrically quantified PM lost from the DPF during
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regeneration to calculate the fraction of trapped PM oxidized to CO, CO2, and gas-phase total
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hydrocarbons (THC).
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The DPF was physically removed from the truck and weighed three times during each
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regeneration cycle, including before loading with engine-out PM, after loading but before
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regeneration, and after regeneration. This allows determination of DPF mass loading per mile
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driven and mass lost from the DPF during regeneration. After being removed from the vehicle,
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both the inlet and outlet of DPF were sealed with aluminum foil to avoid contamination.
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Gravimetric masses were recorded after an overnight soak, which allowed internal DPF
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temperature to decrease to ambient levels. Masses were determined to the gram with a large
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package balance with a resolution of 0.1 g (model LP34001P, Sartorius, Bohemia, NY). Masses
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of the unloaded and loaded 2007 DPF ranged from 21.959 to 21.964 kg and 22.098 to 22.128 kg,
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respectively. For the 2010 DPF, these ranges were 20.699 to 20.720 and 20.723 to 20.826 kg.
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The “efficiency” of PM elimination during DPF regeneration was calculated using the mass
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PM emitted and either the mass lost from the DPF, or the fuel injected into the aftertreatment
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during active regeneration. If the PM emitted during regeneration is assumed to arise entirely
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from PM trapped in the DPF, it can be divided by the total mass lost from the DPF during
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regeneration to determine the DPF filtering efficiency accounting for regeneration:
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regen = 1 − PM emitted⁄DPF mass lost
(1)
DPF mass lost is the difference in DPF mass before and after regeneration, and thus regen is
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the probability that PM trapped by the DPF will not be subsequently released as PM during
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regeneration. In an alternate calculation, the PM emitted during regenerations was assumed to
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arise entirely from fuel injected into the HDDV aftertreatment to raise the DPF temperature to
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~500 °C during regeneration. The PM emitted was then divided by the total quantity of fuel
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added to the aftertreatment to determine the aftertreatment combustion fraction (ACF):
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ACF = 1 − PM emitted⁄fuel injected into aftertreatment
(2)
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Fuel injected into the aftertreatment was determined from either SPN 3522 or 3481 (defined in
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the SAE J1939 protocol) from the vehicle’s OBD system. We note that neither of these
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assumptions is completely valid, as PM emitted during regeneration arises both from PM stored
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in the DPF and that created by incomplete combustion of fuel injected into the aftertreatment
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during regeneration. Also, because fuel is not injected into the aftertreatment during passive
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regenerations, ACF was only determined for active regenerations.
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In addition to the characterization of emissions during individual DPF regeneration
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events, we analyzed activity data collected from a set of 85 heavy-duty diesel vehicles, each
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either Class 7 or Class 8, representing ten vocations. This data was collected with J1939 Mini
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LoggersTM (HEM Data, Southfield, MI) which record both global positioning satellite (GPS)
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coordinates and ECU parameters. Data was recorded at 1-second intervals, and all points with
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engine RPM < 300 were discarded to ensure that only “engine-on” conditions were sampled. The
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total engine-on time recorded was 26,526 hours, and the total distance travelled during recording
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was 489,327 miles.
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Table 1. ECU parameters used to identify active regenerations, in order of precedence. SPN name
SPN #
# HDDVs
Aftertreatment 1 Total Fuel 3522 Used
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Aftertreatment 1 Fuel Rate
3481
6
Fuel 3480
1
Aftertreatment 1 Diesel 3721 Particulate Filter Time Since Last Active Regeneration
1
Aftertreatment Diesel 3700 Particulate Filter Active Regeneration Status
21
Aftertreatment Pressure 1
1
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Several ECU fields were used to determine when an active DPF regeneration was occurring.
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Table 1 lists these fields in order of precedence. For example, fields that reported the amount of
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fuel injected into the DPF were considered the most reliable, and were used whenever they
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included reliable data. Also, the Wheel-Based Vehicle Speed (SPN #84) was used to determine
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the total distance travelled between active regenerations. Of the 85 HDDVs, 71 recorded at least
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one DPF regeneration event as determined by at least one of the fields in Table 1. 67 HDDVs
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recorded at least two DPF regenerations, and could therefore be used to calculate regeneration
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frequency.
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RESULTS AND DISCUSSION
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Figure 1. (a) Engine parameters and (b) emissions during a parked regeneration of the 2007
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HDDV DPF, performed on April 23, 2015.
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Figures 1 and 2 display time series of engine parameters and emissions during a typical parked
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and a typical driving regeneration, respectively. Analogous plots for all other regenerations can
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be found in Figures 4 and S2 – S9. Emissions of gas-phase species, including NOx and
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hydrocarbons (HC), occurred primarily during the first few minutes of the regeneration, before
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aftertreatment temperatures reached their maximum values. Particulate emissions were also
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distinct during this early phase, having greater diameters (~60 nm) compared those later in the
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test with diameters of 30 nm or less.13,15
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Figure 2. (a) Engine parameters and (b) emissions during a driving regeneration of the 2010
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HDDV DPF, performed on August 26, 2015.
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Table 2. DPF mass balance during each regeneration. Test Date
MY
Type
DPF mass PM emitteda losta
regen
Regeneration fuel
AF
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g
g
%
gal
2/25/2015 2007 parked
168.4
0.72
99.6
3/18/2015 2007 parked
137.1
0.98
99.3
2.62
99.99%
4/23/2015 2007 parked
136.5
5.40
96.0
2.87
99.93%
5/12/2015 2007 driving
100.9
1.87
98.1
0.61
99.89%
5/29/2015 2007 driving
141.9
4.08
97.1
0.83
99.82%
7/15/2015 2010 parked
120.3
2.61
97.8
2.33
99.96%
8/5/2015
2010 driving
93.6
16.33
82.6
2.06
99.71%
8/26/2015 2010 driving
87.0
9.44
89.2
1.22
99.72%
9/15/2015 2010 passive 24.4
0.16
99.4
N/A
N/A
99.99%
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Active regeneration emissions are listed for each test in Table S2, and average values grouped
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by chassis MY and type (parked or driving) are given in Table S3. Engine-out PM during DPF
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loading ranged from 130 to 550 mg/mile driven. This quantity was determined by gravimetric
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analysis of the DPF before and after loading, and so it only includes the overwhelming majority
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of PM trapped by the DPF. Most of this 87 to 168 g was removed from the DPF during
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regeneration. The mass balance of each DPF during regeneration is presented in Table 2. Note
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that the emissions from road regenerations includes those arising from driving the vehicle at 50
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mph, as well as active regeneration. Table 2 includes the efficiency of PM elimination in terms
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of both DPF mass lost (regen ), which ranged from 82.6 to 99.6%, and fuel injected into the
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aftertreatment (ACF ), which ranged from 99.71 to 99.99%. For seven out of nine tests, regen >
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95% and ACF > 99.8%. The two exceptions were the two road regenerations of the 2010 HDDV.
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For these two tests, regen was reduced to 83 – 89% and ACF was reduced to 99.7%.
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The carbon dioxide associated with the decrease in DPF mass was minor compared to that
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generated by fuel combustion during regeneration, which ranged from 10 to 29 kg C. Other
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forms of emitted gas-phase carbon, including carbon monoxide and hydrocarbons, were also
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minor (35 to 92 g and less than 5 g, respectively). Typically less than 5 g particulate matter was
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emitted during each regeneration (Table S2), and it was dominated by ultrafine (D < 100nm)
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sulfate. Again, the exceptions were the active road regenerations of the 2010 HDDV, which
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emitted 9-16 g PM. These events involved larger particles (40-50 nm) and increased black
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carbon emissions.15
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Gravimetric analysis of the DPF before and after each regeneration event (Table 2) allowed for
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both derivation of DPF inlet (i.e., engine-out) PM and of the overall ability of the DPF to
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eliminate particulate emissions (e.g., regen ). (Note that this definition of “engine-out” only
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includes PM that remains trapped in the DPF, and therefore does not include any PM that
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evaporates from the DPF.) Engine-out PM was highest (491 – 548 mg/mi) for loading of the first
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two DPF regenerations, in which dynamometer force and thus engine loading were kept low.
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Engine loading was subsequently increased, which caused a decrease in engine-out PM from
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~500 to ~250 mg/mile (Table S2). The much higher values for the first two tests demonstrate the
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differences in HDDV engine-out PM with changing duty cycle, and suggest that differences in
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these cycles will influence the frequency of, and perhaps the emissions associated with, DPF
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regenerations. Additionally, lower engine-out PM emissions ranging from 126 - 229 mg/mi were
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reported for the truck with a MY 2010 engine (161 mg/mi) compared to 238 - 265 the truck with
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the MY 2007 engine under similar loading conditions (Table S2). This suggests that a physical
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failure of the DPF on a MY 2007 engine would result in a greater emissions impact than an
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equivalent failure on a MY 2010 engine.
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During active regenerations, PM emissions were dominated by sulfate. During passive
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regenerations, much less PM was emitted, and it was dominated by organic matter (Fig. 3).
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Although a greater proportion of the passive emissions was organic, the absolute amount of
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organic carbon emitted was similar during active (0.03 to 0.38 g) and passive (0.05 to 0.17 g)
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regenerations. PM emitted during active regenerations ranged from 0.72 to 16.3 g, and the
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portion of this gravimetric mass that was speciated ranged from 43 to 125% (average 70%). For
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the passive regenerations, gravimetric PM emitted ranged from 0.10 to 0.22 g, 33 – 126% of
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which was speciated (average 88%). Gravimetric mass that was not speciated could either be in
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species that were not analyzed, or could have been lost from the filters before analysis. The ratio
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of detected sulfate-S (by ion chromatography) to detected sulfur (by x-ray fluorescence) was
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47% (Fig. S10). This indicates that less than half of the sulfur emitted was in the form of water-
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soluble sulfate, and the remaining non-sulfate sulfur could be responsible for much of the
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“missing” gravimetric mass. Other material that could contribute to unspeciated mass include
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organic oxygen, nitrogen, etc., as well as insoluble inorganic ions.
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Figure 3. Chemical composition of PM emission during active and passive HDDV
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regenerations. Note the split y scale.
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The PM emitted during active regenerations ranged from 0.2 to 5.4 g, except for the active
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driving regenerations of the 2010 DPF. During these two tests, 9.4 and 16.3 g PM were emitted.
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Correspondingly, regen was over 97% for all tests except for these two with relatively high PM
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emissions, when it was 90 and 82%. About half of the emitted gravimetric mass could be
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accounted for by sulfate (Fig. 3), which ranged from 0.6 to 6.2 g per regeneration (Table S2).
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The maximum sulfur content of the ULSD used in this study is 15 ppm. The amount of this fuel
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used for active regenerations ranged from 0.61 to 2.87 gallons, with generally higher amounts for
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driving regenerations. This corresponds to a maximum amount of sulfur in this fuel of 0.03 to
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0.14 g. Because the sulfur emitted during regenerations is much higher than the amount in fuel
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burnt during these events, it must derive from fuel and/or oil burned during DPF loading and
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stored in the aftertreatment,16-18 or from oil burned during the event. This sulfur is released only
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when aftertreatment temperatures are high, or similar to typical regeneration temperatures. XRF
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measurements suggested particulate sulfur in other forms, perhaps organosulfates, contributed to
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emitted PM (Fig. S10). Recent work has highlighted the formation of organosulfates in
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secondary organic aerosol formation from diesel fuel,19 and the results of this study suggest that
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future work should also attempt identify these compounds in primary emissions from modern
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HDDVs.
(a)
(b)
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Figure 4. (a) Engine parameters and (b) emissions from a driving regeneration of the DPF from
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the 2010 HDDV performed on August 5, 2015.
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PM emissions were much lower during passive regenerations of the 2010 DPF (Fig. 3). This
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PM had much lower sulfur fractions than all active regenerations. This most likely results from
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the difference in aftertreatment temperature between passive and active events and/or the
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differences in chemistry (unlike active regeneration, NO2 is the dominant oxidant during passive
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regeneration). During passive events, the HDDV was driven at a constant speed of 50 mph, and
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temperature throughout the aftertreatment plateaued at about 400°C (Figs. S7-S9). The
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maximum aftertreatment temperature during active regenerations was about 100°C greater than
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passive regenerations (Figs. 2, 4). The lower temperatures during passive regeneration could
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have prevented stored sulfur from being oxidized and/or volatilized. This lower temperature did
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not inhibit the effectiveness of the regeneration, however: regen was 99.4% during the one event
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for which it was quantified, which is at the upper end of the range of regen observed for active
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regenerations (Table 2). Given the fuel penalty associated with active regeneration, these results
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demonstrate that passive regenerations are preferable to active regenerations of HDDV DPFs
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from a fuel consumption perspective. While such passive regenerations are able to remove stored
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carbonaceous material, however, they may not be able to remove stored sulfur as effectively. It is
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also possible, however, that passive regenerations release sulfur as SO2 (i.e., without oxidizing it
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to SO3). Because sulfur has the potential to poison catalysts,20 future work should focus on the
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chemistry of the sulfur storage process and sulfur oxidation during both active and passive
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regenerations.
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Figure 5. Chemical composition of size-segregated PM emitted during a passive regeneration,
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followed by two forced regenerations, of the 2010 DPF.
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Inorganic PM composition as a function of particle size was determined during one of the
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regenerations of the DPF on the 2010 HDDV (Fig. 5). These samples were also dominated by
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sulfate, which was distributed approximately equally between the nucleation mode (Dp ~ 30 nm
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and below) and accumulation mode (Dp ~ 100 nm). Ammonium was also present in these
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particles, although not in sufficient quantity to fully neutralize the sulfate - NH4+:SO42- ratios
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ranged from 0.05 to 0.90 (Fig. 5), whereas an NH4+:SO42- ratio of 2 corresponds to full
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neutralization. In general, the size-segregated samples that had the highest sulfate concentrations
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were the least neutralized.
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There are three general explanations for the relatively high PM emissions during road regenerations of the 2010 DPF. First, the added surface area associated with the SCR could allow
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for more storage of sulfur in the 2010 aftertreatment. However, much less PM (2.61 g) was
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emitted during a parked regeneration of the 2010 DPF. Furthermore, carbonaceous emissions
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were also elevated in the 2010 driving regenerations relative to other events (Fig. 3, Table S2).
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Thus, while sulfur storage in the DPF may explain part of these anomalously high emissions,
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there must be other major contributions. A second potential cause is incomplete combustion of
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(carbonaceous) PM stored in the DPF, and a third is incomplete combustion of fuel injected into
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the aftertreatment during regeneration. Either of both of these could contribute to the higher CO
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emissions during road regenerations of the 2010 DPF (51 – 92g) relative to parked 2010 and all
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2007 regenerations (5 – 35 g) (Table S2).
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Gas-phase emissions during the beginning of regenerations events, when aftertreatment
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temperatures increase sharply, provide insight into the relatively high PM emissions during
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driving regenerations of the 2010 HDDV. As the first such test was initiated, a ~2 minute spike
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in HC emissions was seen, similar to all other tests (Fig. 4). However several minutes later, HC
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emission increased again, something generally not seen in the parked test or in either driving or
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parked tests of the 2007 HDDV. NOx emissions were relatively low during this increase in HC
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emissions, suggesting that either stored PM or fuel injected into the aftertreatment was not being
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completely combusted. A similar pattern was seen during the second 2010 driving regeneration
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(Fig. 2), although the HC emitted, as well as the PM, was lower. The overall pattern of increased
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HC emissions at the beginning of a regeneration event, and increased particle number emissions
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towards the end, was also observed recently for heavy-duty diesel trucks with similar
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aftertreatment systems but certified to Japanese emissions standards.21
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Nucleation mode particles have often been observed during active regeneration of DPFs, including those on light-duty vehicles22 and from heavy-duty engines.23 The median diameter of
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particulate emissions during active parked regenerations of the same 2007 and 2010 HDDVs
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used in this study was below 30 nm during the later stages of these events.12 The promotion of
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homogeneous particle nucleation by lowered particle surface area for competing heterogeneous
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nucleation is also consistent with the inverse relationship between particle number and volume
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observed during a series of consecutive DPF regenerations (Fig. S11, note that such repeated
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regenerations are not expected to be representative of real-world use.Furthermore, the relatively
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low ammonium to sulfate ratios observed in this study (Fig. 5) are consistent with observations
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of gaseous sulfuric acid in DPF-equipped heavy-duty engine exhaust.24
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Of the 71 on-road vocational HDDVs that logged at least one DPF regeneration, most were
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actively regenerating between 1 and 3% of engine-on time (Fig. S12, based on SPN 3100). A
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small number of HDDVs were actively regenerating their DPFs greater than 5% of the time their
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engines were on. These HDDVs had lower DPF outlet temperatures during regeneration,
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suggesting inhibited fuel injection into the aftertreatment (Fig. S13). However, removal of these
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HDDVs did not significantly change the average frequency of DPF regeneration among the
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entire fleet. On average, these HDDVs underwent active DPF regeneration every 28.0 ± 2.5
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hours the engine was on, or every 599 ± 95 miles the truck traveled (all quoted uncertainties are
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the standard error of the mean). Generally, HDDVs with higher average vehicle speeds (such as
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line haul trucks) had longer time periods (Fig. S14) and distance travelled (Fig. S15) between
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regenerations.
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The observations of real-world regeneration frequency suggest that PM emitted during
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regeneration will be comparable to or less than that emitted during “normal” (non-regenerating)
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operation. A recent study of on-road heavy-duty truck emissions in CA found that HDDV PM
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emissions ranged from 4 to 14 mg/mi.25 Given that the average distance travelled by the
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vocational HDDV fleet between regenerations was 599 miles, this would be equivalent to 2.4 –
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8.4 g of emitted PM during regeneration events. The range of PM emitted during these
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regeneration events was 0.7 to 16 g, suggesting that while PM emitted during regeneration can
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be more variable, it is on average roughly equivalent to PM emitted during normal operation.
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Therefore, if a properly functioning DPF removes 99% of engine-out PM during non-
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regenerating operation, accounting for regeneration PM will lower this number at most to 98%.
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The minor influence of regeneration PM on overall emissions is also reflected in the observation
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that regeneration PM represents less than 0.3% of total PM stored in the DPF (Table 2).
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As illustrated in Figure S14, the average time between regeneration events for the 67 HDDVs
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for which this quantity could be derived ranged from 11,451 to 363,012 seconds. The FTP cycle
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used during certification of HDD engines has a length of 1200 seconds. Thus the real-world
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regeneration frequencies reported here suggest that active regenerations may occur, on average,
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in anywhere between 10 and 300 FTP cycles, which is consistent with results from the Advanced
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Collaborative Emission Study.26,27 There was even greater variability in the average road
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distance traveled between regenerations (Fig. S15). This wide range in regeneration frequency,
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seen even within specific vocations, demonstrates the adaptability required of advanced control
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systems to effectively monitor and ensure the proper operation of the DPF. It also represents a
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challenge for regulators attempting to select driving cycles representative of real-world HDDV
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operation.
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ASSOCIATED CONTENT
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Supporting Information.
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Description of DPF loading procedure
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Description of real-time instrumentation
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Description of PM filter collection and analysis
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Figure S1. Typical pattern of acceleration/deceleration used to load HDDV DPFs with PM.
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Figure S2. (a) Engine parameters and (b) emissions from a parked regeneration of the DPF
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from the 2007 HDDV performed on February 25, 2015. Figure S3. (a) Engine parameters and (b) emissions from a parked regeneration of the DPF from the 2007 HDDV performed on March 18, 2015. Figure S4. (a) Engine parameters and (b) emissions from a driving regeneration of the DPF from the 2007 HDDV performed on May 12, 2015. Figure S5. (a) Engine parameters and (b) emissions from a driving regeneration of the DPF from the 2007 HDDV performed on May 29, 2015. Figure S6. (a) Engine parameters and (b) emissions from a parked regeneration of the DPF from the 2010 HDDV performed on July 15, 2015. Figure S7. (a) Engine parameters and (b) emissions from a passive regeneration of the DPF from the 2010 HDDV performed on September 15, 2015. Figure S8. (a) Engine parameters and (b) emissions from a passive regeneration of the DPF from the 2010 HDDV performed on September 17, 2015. Figure S9. (a) Engine parameters and (b) emissions from a passive regeneration of the DPF from the 2010 HDDV performed on September 22, 2015.
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Figure S10. Sulfur detected by IC (as sulfate) vs detected by XRF.
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Figure S11. Results from four consecutive forced regenerations of the DPF on the 2007
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HDDV. SMPS results are presented as (a) number size distributions, (b) total volume
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concentration, and (c) total number concentration.
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Figure S12. Histogram of the percentage of total running time that real-world vocational HDDVs underwent active DPF regeneration. Figure S13. Fraction of engine-on time in which active DPF regeneration was occurring vs. average DPF outlet temperature during regeneration. Figure S14. Average engine-on time between DPF regenerations, by HDDV vocation, model year (symbol), and OEM (color). Figure S15. Average distance travelled between DPF regenerations, by HDDV vocation, model year (symbol), and OEM (color).
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Table S1. Heavy-Duty Diesel Vehicle Specifications.
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Table S2. Summary of active regeneration tests, emissions, and DPF loading conditions.
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Table S3. Emissions and DPF mass lost during active regenerations. This is the same data as in
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Table S2, but grouped first by Model Year and then by type (parked or driving).
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AUTHOR INFORMATION
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Corresponding Author
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*Chris R Ruehl
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Email:
[email protected] 455
Phone: (916) 323 - 1520
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ACKNOWLEDGMENT
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The authors would like to thank William Robertson (CARB) for insightful comments on an
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earlier draft that improved the manuscript.
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TABLE OF CONTENTS (TOC) ART
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