Subscriber access provided by UNIV OF NEW ENGLAND ARMIDALE
Energy and the Environment
Impacts of alternative fuels on morphological and nano-structural characteristics of soot emissions from an aviation piston engine Longfei Chen, Xuehuan Hu, Jing Wang, and Youxing Yu Environ. Sci. Technol., Just Accepted Manuscript • Publication Date (Web): 25 Mar 2019 Downloaded from http://pubs.acs.org on March 25, 2019
Just Accepted “Just Accepted” manuscripts have been peer-reviewed and accepted for publication. They are posted online prior to technical editing, formatting for publication and author proofing. The American Chemical Society provides “Just Accepted” as a service to the research community to expedite the dissemination of scientific material as soon as possible after acceptance. “Just Accepted” manuscripts appear in full in PDF format accompanied by an HTML abstract. “Just Accepted” manuscripts have been fully peer reviewed, but should not be considered the official version of record. They are citable by the Digital Object Identifier (DOI®). “Just Accepted” is an optional service offered to authors. Therefore, the “Just Accepted” Web site may not include all articles that will be published in the journal. After a manuscript is technically edited and formatted, it will be removed from the “Just Accepted” Web site and published as an ASAP article. Note that technical editing may introduce minor changes to the manuscript text and/or graphics which could affect content, and all legal disclaimers and ethical guidelines that apply to the journal pertain. ACS cannot be held responsible for errors or consequences arising from the use of information contained in these “Just Accepted” manuscripts.
is published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society. Copyright © American Chemical Society. However, no copyright claim is made to original U.S. Government works, or works produced by employees of any Commonwealth realm Crown government in the course of their duties.
Page 1 of 21
Environmental Science & Technology
1
Impacts of alternative fuels on morphological and nano-structural
2
characteristics of soot emissions from an aviation piston engine Longfei Chen,† Xuehuan Hu,† Jing Wang,,
3
4
† Department
5
‡
6
8093 Zurich, Switzerland
7
§
8
Science and Technology, 8600 Dübendorf, Switzerland
9
∥
‡, §,
Youxing Yu∥
of Energy and Power Engineering, Beihang University, 100083 Beijing, China
Institute of Environmental Engineering, ETH Zurich - Swiss Federal Institute of Technology Zurich,
Laboratory for Advanced Analytical Technologies, Empa - Swiss Federal Laboratories for Materials
Department of Materials Science and Engineering, Beihang University, 100083 Beijing, China
10
ABSTRACT:
Soot
emissions
from
11
aviation piston engines (APEs) are a major
12
source of environment pollutions in airport
13
vicinity, stratosphere and troposphere, and
14
their nano-structure and surface chemistry
15
play a critical role in determining the impact on human health and environment. In this work,
16
the morphology and nano-structure of soot emitted from an aviation piston engine burning five
17
different fuels including blends of promising alternative jet and biofuels were investigated via
18
high-resolution transmission electron microscopy (HRTEM) and Raman spectroscopy. The
19
graphitic structures were observed by analyzing primary particles in the HRTEM images.
20
Morphological analysis demonstrated that the separation distance of the graphene layers of soot 1 / 21
ACS Paragon Plus Environment
Environmental Science & Technology
Page 2 of 21
21
particles from kerosene-pentanol blend combustion was larger than that from kerosene-Fischer-
22
Tropsch blend combustion, indicating that adding pentanol tended to generate particles with
23
more loosely stacked layers and higher oxidation tendency. Raman results were in agreement
24
with primary particle nano-structure analysis based on the HRTEM images. Furthermore, soot
25
particles from different fuels exhibited different concentrations of amorphous carbon and
26
structural defects.
27
28
Aviation soot emissions have become a significant contributor to particulate matter (PM)
29
emissions in upper troposphere, lower stratosphere and airport areas 1. Ultrafine particles and
30
the secondary organic aerosols (SOA) from aircrafts are the dominant pollution sources in the
31
upper air and have direct consequences for haze weather 2. Furthermore, aircraft particle
32
emissions can cause ice nucleation for cloud formation, which affects solar radiative forcing 3
33
and thus could influence global climate pattern
34
lower airspace than commercial aviation aircrafts, and aviation piston engines (APEs) as the
35
major power units emit soot particles within troposphere which are closer to the ground
36
Piston aircraft shipments reached 1,085 units in 2017 (out of 2,324 total general aviation aircraft
37
shipments) and are forcast to increase by 0.3% per year in the U.S. by General Aviation
38
Manufacturers Association (GAMA).7 Soot emissions from APEs may gain increasing attention
39
due to the forthcoming aviation emission regulations and huge potential markets triggered by
40
gradual airspace openness in developing countries like China 7. APEs have low combustion
41
efficiency and simple analog controls which lead to different emissions characteristics and
INTRODUCTION
4-5.
General aviation aircrafts normally fly in
2 / 21
ACS Paragon Plus Environment
6-7.
Page 3 of 21
Environmental Science & Technology
42
amounts than the turbine engines. Piston engines emit more carbon monoxide and hydrocarbons
43
and less nitrogen oxide8. However, there is little research to analyze emission differences
44
between piston and gas turbine engines.
45
The depletion of fossil fuel resources, the steadily increasing cost of crude oil and the
46
requirment for energy independence have given impetus to the search for alternative aviation
47
fuels. Alternative fuels can reduce particulate matter (PM) emissions with little impact on
48
aircraft engine operation and performance 9. The second International Civil Aviation
49
Organization (ICAO) conference on aviation and alternative fuels in 2017, with the aim of
50
developing an ICAO vision on aviation alternative fuels, encouraged further development of
51
aviation alternative fuels 10. A ‘single fuel policy’ was proposed
52
diesel or kerosene) could be widely used to replace currently mainstream AVGAS (aviation
53
gasoline) for APEs due to safty and logistical concerns 12. Other promising alternative aviation
54
fuels include Fischer-Tropsch (F-T) fuels and biofuels. The F-T synthesized fuels, which have
55
been certified in civil aviation (mainly gas turbine engines) for decades 13, exhibit properties
56
substantially similar to historically refined kerosene, because specifications (such as D7566 and
57
D1655) guide the production of the synthesized fuels that are compositionally similar to the
58
conventional kerosene. Another paraffin-based alternative fuel (Hydrotreated Ester and Fatty
59
Acids, HEFA) is produced via hydrotreatment of biomass sources and is also chemically similar
60
to F-T fuels 14-15. Furthermore, pentanol as a high-carbon alcohol has the virtues of larger energy
61
density and better miscibility with hydrocarbons compared with low-carbon alcohols 16-17. The
62
blends of pentanol and hydrocarbon aviation fuels could be considered as an alternative aviation
63
fuel and have gradually gained acceptance 18. In terms of aviation kerosene, previous studies 3 / 21
ACS Paragon Plus Environment
11
and heavy fuels (such as
Environmental Science & Technology
Page 4 of 21
64
mainly used Jet A or Jet A-1 type (common commercial aviation fuels in the U.S.), but RP-3
65
was rarely investigated, which is widely used in Chinese aviation industry. It is desirable to
66
expand the database of RP-3 because of the noticeable difference between RP-3 and well-
67
studied kerosenes in terms of aromatic hydrocarbon content and flash point
68
assess the potential effects of alternative aviation fuels on environment and health, thoroughly
69
investigating the morphology and nano-structure characteristics of their PM emissions is crucial,
70
because these characteristics of particles are closely linked to their ice nucleation potential (ice
71
freezing microphysics) and oxidative reactivity
72
understanding of soot formation 4.
21,
19-20.
To better
and could enhance the fundamental
73
High-resolution Transmission Electron Microscope (HRTEM) images are commonly used
74
to determine the nano-structure characteristics such as fringe length, fringe separation distance
75
and fringe tortuosity
76
information
77
microscopically structural defects of soot samples 25. It was reported that oxidation-promoting
78
and oxidation-inhibiting morphological features could be measured by Raman spectrum 26. The
79
oxidation rate of soot particles could differ by nearly 400%, depending on the nano-structure
80
of primary particles 27.
24,
22-23.
Raman spectral analysis could also provide soot nano-structural
and could provide detailed information about graphitization degree and
81
Diesel particles have been extensively studied using HRTEM and Raman analysis. Graphitic
82
crystallite structures observed by HRTEM and Raman spectra revealed details of the graphite
83
structures quantitatively 28 and the degree of the crystalline structures increased as the engine
84
load increased. Previous studies demonstrated that the lube oil-derived particles had more
85
disordered structures than diesel particles according to HRTEM images, and more defective 4 / 21
ACS Paragon Plus Environment
Page 5 of 21
Environmental Science & Technology
86
bands in lube oil-derived particles were revealed by Raman spectrum 29. Aviation particles were
87
characterized mainly in the metric of particle mass or number, yet only a few studies focused
88
on the nano-structure characteristics of turbofan aero-engine particles
89
significant difference regarding the combustion systems among the gas turbine engines,
90
vehicular engines and APEs, it is desirable to fill the gap by comprehensively characterizing
91
the nano-structure and reactivity of soot emissions from APEs to better assess their impact on
92
climate and environment. To the authors’ best knowledge, there is no open literature on the
93
morphology and nano-structure characteristics of soot emissions from APEs. In this study,
94
Chinese kerosene RP-3, promising alternative aviation fuels and their blends were used to
95
characterize the APE soot emissions microscopically via HRTEM and Raman spectroscopy.
96
21, 30.
Due to the
MATERIALS AND METHODS
97
Test Rig. Currently, there are two types of APE engines, namely, spark-ignition engines and
98
compression-ignition engines. A two-stroke, compression-ignition aviation piston engine with
99
a supercharging system and a swirl scavenging system was utilized to produce particle
100
emissions. The engine specifications are listed in Table S1 of Supporting Information. The
101
engine was controlled by a transient dynamometer, and the soot sampling was achieved using
102
a modified exhaust pipe with a controlled dilution system including a filter holder (SI Figure
103
S1). Soot samples were collected under two steady conditions at the constant engine speed of
104
1600 rpm with two different engine loads of 2 bar and 8 bar brake mean effective pressure
105
(BMEP). All the PM were sampled at the steady-state after engine warm-up. Soot particles were
106
collected on the quartz fiber filters in an unheated filter holder (GE Whatman, 47mm). We
5 / 21
ACS Paragon Plus Environment
Environmental Science & Technology
107
chose three or four areas of each grid (300 mesh, 20-nm-thick carbon lacey) to ensure that the
108
analyzed particles were representative. The microscopic analysis method is explained in
109
Supporting Information.
110
119
Page 6 of 21
Test Fuels. The properties of diesel, RP-3 kerosene and Fischer-Tropsch and their blends 31-32.
111
were computed according to the literature
Apart from diesel and RP-3, three different
112
blends, namely, R80P20 (80% RP-3, 20% pentanol by volume), R60P40 (60% RP-3, 40%
113
pentanol by volume) and R75F25 (75% RP-3, 25% Fischer-Tropsch in volume) were prepared.
114
Kerosene has less carbon atoms, lower distillation temperature range, lower cetane number and
115
lower viscosity than diesel. Meanwhile, kerosene has better atomization compared with diesel
116
due to its lower viscosity, surface tension and density. Pentanol was added to RP-3 to increase
117
the viscosity and the oxygen content. The primary properties of the five test fuels are listed in
118
Table 1. Table 1 Fuel properties of the baseline diesel, RP-3, Pentanol, Fischer-Tropsch and the test blend fuels. Diesel RP-3 Pentanol R80P20 R60P40 FischerFuel types Tropsch Carbon number per molecule C16-C23 C8-C12 C5H12O --C9-C20 or chemical formula Viscosity (mm2/s) 4.13 1.28 2.89 1.602 1.924 2.1261 Density (g/cc) 0.83 0.79 0.815 0.803 0.806 0.7561 Cetane number 56.50 42.00 20-25 37.6-38.6 33.2-35.2 67.2 Lower heating value (MJ/kg) 42.68 43.43 35.06 41.731 40.044 -Oxygen content (wt%) 0.00 0.00 18.18 3.636 7.272 5.617 Latent heating (kJ/kg) 270 -308 ---Surface tension (10-3 Nm-1) 27.50 23.60 24.7 23.82 24.04 -Sulphur (%) 0.50 0.30 0.00 0.24 0.18 0.00 Boiling point (℃) T10=223 T10=172.8 138 ---T50=266 T50=194.9 ---T90=311 T90=224.4 ----
R75F25 C9-C20 1.5315 0.76 49.2 -1.405 --0.00 ----
120
Raman Experiments. A Raman spectrometer (Horiba Jobin-Yvon LabRAM HR800) was used for
121
analyzing soot samples deposited on quartz filters. The excitation laser of 633 nm was Ar-ion type. A
122
low laser power of 1.36 mW was used to eliminate overheating. The diameter of the laser spot was 2 6 / 21
ACS Paragon Plus Environment
Page 7 of 21
Environmental Science & Technology
123
μm and the slit size of the fully focused laser beam was 25 μm. Each spectrum was obtained from two
124
repetitive 10 s accumulation. The Raman spectra were obtained with the range between 800 to 2000
125
cm-1. Statistical analysis was based on three areas for each sample.
126
For samples that were collected on filters, a large number of Raman spectra were obtained and
127
averaged to obtain the mean values. Quantifying the five bands of Raman spectra provided detailed
128
information about the chemical composition of soot emitted from APEs. All Raman spectra were
129
processed by the embedded ‘Lebspec5’ software, which also performed curve fitting for determining
130
the spectral parameters. Figure 1 illustrates a typical spectrum after baseline correction and the fitted
131
curve with the combination of four Lorentzian-shaped G, D1, D2, D4 bands at about 1580, 1340, 1620,
132
1180 cm-1 and the Gaussian-shaped D3 band at about 1500 cm-1 33. Table 2 presents physical meanings
133
of the bands.
134 135 136
Figure 1. Typical Raman spectrum and curve fitting for diesel particles at 2 bar BMEP. Table 2. Spectroscopic origins of the Raman spectra bands Band
Center
Formula
Origin
D1
1350cm-1
Lorentzian
Defects occurring at the vibrational mode involving A1g-sym metry (graphene layer edges) or A2 transition 34
D2
1620cm-1
Lorentzian
Associated with the disordered graphitic crystal (E2g-symmet ry and surface) 33
7 / 21
ACS Paragon Plus Environment
Environmental Science & Technology
D3
1500cm-1
Gaussian
Related to the amorphous carbon content (such as functional groups and organic molecules) 33, as well as the internal vibrational modes of tiny graphitic crystals related to the C– C stretching and edge carbons 21.
D4
1200cm-1
Lorentzian
Related to the vibrations of sp2- and sp3-hybridized carbon bonds, A1g symmetry (disordered graphite lattices), ionic impurities, and C-C and C=C stretching vibrations of polyenes 35-36.
G
1580cm-1
Lorentzian
The ideal graphitic crystal stretching mode 34.
Page 8 of 21
137
HRTEM Measurements. Soot samples were analyzed using a high-resolution TEM (JEM-2100F,
138
Japan), operating at 200kV with a spatial resolution of 0.23 nm. The maximum magnification of TEM
139
images was 1,500,000×. Soot was deposited on TEM grids (20-nm-thick carbon lacey coated Cu grids,
140
Spi Supplies). The TEM image processing regarding the fringe characteristics (such as the fringe
141
distance, length, tortuosity and separation distance) was achieved using an in-house MATLAB code
142
developed by following the existing algorithm
143
distributions were obtained by quantifying over two hundred primary particles of each aggregate
144
particle using the in-house MATLAB-based software. Four or five locations were randomly chosen
145
on each filter. Part of the particle-loaded filter was extracted in a beaker with ethanol solution. Then
146
the filter was placed in an ultrasonic oscillator bath for over 30 minutes. The filter was taken out from
147
the solution and 7-8 drops of the colloidal solution were placed on the TEM grid (300 mesh, 20-nm-
148
thick carbon lacey) and then dried in the beaker under gentle air flow and light. In this study, the fringe
149
length was treated as the size of the carbon layer 38, fringe distance was defined as the straight-line
150
distance between the two ends of a carbon layer, and the fringe tortuosity was characterized as the
151
ratio between the fringe length and the fringe distance. The mean distance between two adjacent layers
152
was measured as the fringe separation distance 38, which was illustrated in Figure 2 (c).
37
as shown in Figure 2. Primary particle size
8 / 21
ACS Paragon Plus Environment
Page 9 of 21
Environmental Science & Technology
153
154 155 156
Figure 2. Post-processing of HRTEM images via fringe analysis: (a) the original image; (b) the fringe skeleton image; (c) the metrics of fringe characteristics.
157
RESULTS AND DISCUSSION
158
Soot Morphology and Nano-structure Characteristics. Figure 3 shows the HRTEM images of
159
soot particles from the engine at 8 bar BMEP for three different fuels (RP-3, R80P20 and R75F25).
160
Volatile organic compounds (VOC) overwhelmed particulate matter emissions at low engine load of
161
2 bar BMEP, hence the soot fraction was too small to reveal nano-structure information. Figure 3
162
illustrates that similar grape-like aggregates of APE soot particles were observed regardless of
163
different fuels. These aggregates were the collection of small primary particles of 10-30 nm. The
164
images of R80P20 soot particles (e.g. Figure 3b) featured the smallest aggregate particles. Figure 4
165
shows that the size of the R80P20 primary particles ranged from 15 to 25 nm and was smaller than
166
those from the other two fuels, which suggests that pentanol fuel addition may have promoted the
167
oxidation of primary particles and hence reduced the primary particle size. The partially oxidized soot
168
may experience further oxidation, leading to the reduction of the primary particle size and more
169
compacted soot particles through the detachment of the chain-like branches from large aggregates 39.
170
R75F25 generated slightly smaller primary particles than RP-3 which might be attributed to the fact
171
that F-T fuel addition with lower aromatics content suppressed soot formation due to the reduction of
172
soot precursor polycyclic aromatic hydrocarbons (PAHs)
40-42.
9 / 21
ACS Paragon Plus Environment
Smaller particles tend to be more
Environmental Science & Technology
Page 10 of 21
173
reactive than bigger ones because of their lower volume to surface ratio, in other words, smaller
174
particles are more likely to experience oxidation which further modifies the morphological and nano-
175
structural properties 27, 43.
176 177 178
Figure 3. TEM images of representative soot particles and their morphological analysis: (a) RP-3, (b) R80P20, (c) R75F25.
179 180
Figure 4. Size distributions (by frequency obtained via number counting) of the primary particles.
181
Close inspection of the primary particles demonstrated typical core-shell morphology with
182
amorphous (core) and crystalline (shell) regions. The core amorphous region featured turbostratic
183
structure while crystalline domains consisted of distinguishable layers of platelets 44. The TEM images
184
showed that the fuel type did not influence the internal structure of primary particles to an appreciable
185
extent. But oxygenate fuel addition seemed to cause the occurrence of multiple inner cores within a
186
single primary particle, which might be attributable to immediate coalescence prior to a bigger particle
187
being formed from a single core via surface growth 45. Figure 5 also shows that the cores of primary
188
particles generally have higher particle reactivity than that of the outer shell, because the carbon streaks 10 / 21
ACS Paragon Plus Environment
Page 11 of 21
Environmental Science & Technology
189
in the core is shorter than that formed in the shell 27, 38. Among all the test fuels, the soot particles of
190
R80P20 exhibited shorter and more tortuous fringes than RP-3 and R75F25 (Table 3).
191 192 193 194
Figure 5. HRTEM images of representative soot primary particles which have sizes close to the average value for each fuel illustrating nanostructure: (a) RP-3, (b) R80P20, (c) R75F25.
195
to over 200 primary particles for each sample. Fringe parameters are indicative of the graphitization
196
degree and oxidation reactivity of carbonaceous soot 27, 38. Shorter fringe length indicates less graphitic
197
structures with more edge-site carbon atoms that could have highly reactive bonds with adjacent layers
198
46,
199
reactivity because the edge-site carbon atoms of the graphite layers would be more reactive than those
200
within the basal plane 37. The fringe tortuosity of the carbon crystallites could cause the electron orbits
201
in the micro-crystallites to stack and the electrons to repel each other. Thus a repulsive force between
202
adjacent carbon microcrystals arises. The turbostratic stacking of atomic layer planes results in a slight
203
increase in the interlayer distance due to electronic repulsion between molecular orbitals on the
204
adjacent layers 38.
Table 3 lists the fringe characteristics obtained by applying the fringe analysis algorithm (Figure 2)
in contrast, the longer fringe length with lower population of edge-site carbon atoms reduces
205
Higher tortuosity indicates more curved graphene segments and higher reactivity with weaker
206
bonding force between the carbon atoms 46. Oxidizers could access the edge-site atoms through the
207
interlayer spacing, thus the higher fringe separation the higher reactivity would be
208
fringe length is a metric reflecting the size of the plane derived from high-resolution TEM images.
209
Table 3 shows that most fringes were shorter than 2 nm with the fringe separation distance of 0.33 -
210
0.48 nm. The uncertainties of these fringe parameters were all less than the variation between different 11 / 21
ACS Paragon Plus Environment
47-48.
In addition,
Environmental Science & Technology
Page 12 of 21
211
samples which means different fuels had noticeable impacts on soot nanostructure.
212 213
Table 3. The diameter distributions of the primary particles generated by different fuels and nano-structure characteristics based on HRTEM images. Fuel
Average primary particle diameter (nm)
Average fring e length (nm)
Average fringe tortuosit y
Average fringe sep aration distance (n m)
RP-3
24.25 ± 2.64
0.86 ± 0.03
1.20 ± 0.04
0.41 ± 0.03
R80P20
15.95 ± 2.81
0.81 ± 0.03
1.24 ± 0.06
0.46 ± 0.02
R75F25
22.71 ± 2.86
1.02 ± 0.04
1.17 ± 0.06
0.36 ± 0.03
214
Figure 6 illustrates the fringe characteristics of the particles generated by different fuels. It can be
215
seen that the fringe lengths for RP-3 and R80P20 are mainly concentrated at 0.5 nm, while the major
216
fraction of R75F25 fringe lengths are around 0.6 nm. The dependence of the fringe tortuosity on the
217
fuel is different, with the peak fringe tortuosity for R80P20 larger than those for the other fuels. The
218
main findings can be drawn from Table 3 and Figure 6 as follows. Firstly, the R80P20 particles had
219
shorter fringe lengths than the RP-3 and R75F25 particles as shown in Table 3. The longer the fringe
220
length, the larger the graphene layer would be. The R80P20 particles had more disordered layers with
221
more edge-site carbon atoms
222
implied larger curvature of the carbon layers within soot particles that might have been arisen from
223
the reaction of 5-membered rings
224
electronic resonance stabilization 49-50 and individual atoms are more susceptible to oxidative attack.
225
It is for the same reason that fullerenes and carbon nanotubes are more reactive than planar graphite
226
50-51.
46.
Secondly, R80P20 particles had higher fringe tortuosity, which
38.
Higher curvature implies weaker C-C bonds due to lessened
227
The increased fringe tortuosity in the deformed graphite layers would lead to weakened covalent
228
bonds between atoms and increased exposure of the atoms to the oxidizers, therefore higher soot
229
reactivity 38, 52. Thirdly, the separation distances of the R80P20 particles were the largest in Table 3,
230
which indicated that the R80P20 particles had the most loosely stacked layers. The separation distance 12 / 21
ACS Paragon Plus Environment
Page 13 of 21
Environmental Science & Technology
231
was related to the possibility of oxygen to access the edge of the graphite layer. The smaller the
232
distance, the more stable the structure, because less oxygen could access the inner atoms. Therefore,
233
the R80P20 particles were the most likely to be oxidized among the investigated particles.
234 235 236 237
Figure 6. The fringe length and fringe tortuosity histograms analyzed from the primary particles in HRTEM images: (a) Fringe length, (b) Fringe tortuosity. The data with fringe length above 2 nm and fringe tortuosity above 1.52 were truncated because the percentages were too small to be visible on this scale.
238
Raman Spectra of Soot Particles. Raman spectroscopy can be used to characterize crystallite and
239
molecular structures of soot particles 33. Different structural characteristics of PM can be distinguished
240
53 according to the fitted curves from the Raman spectrum (see Figure 1) with different peaks explained
241
in Table 2. It is worth mentioning that the Raman spectra recorded at λ= 633 nm also exhibited second
242
order spectra above 2000 cm-1 Raman shift but only the first order spectra were considered for further
243
analysis.
13 / 21
ACS Paragon Plus Environment
Environmental Science & Technology
Page 14 of 21
244 245 246 247
Figure 7. The area under each band normalized by the total area of all the bands from the fitted Raman spectra. (a) The samples obtained at 2 bar. (b) The samples obtained at 8 bar. The meanings of G (graphite) and D1-D4 (defects) peaks were explained in Table 2.
248
Figure 7 was derived from the Raman spectra of all the sample, which were fitted with five band
249
distributions (the typical first-order Raman spectra of each soot sample can be seen in SI Figure S3).
250
D1 was the most intense band and G and D3 were weaker with D4 and D2 being the weakest. Parent
251
et al.21 studied the soot emissions of a turbofan engine and obtained the band distributions, which
252
showed that the highest intensities occurred at D1 and D3, similar to the RP-3 results in this study.
253
The D3 band at 1500cm-1 was associated with the amorphous carbon, and RP-3 soot exhibited higher
254
amorphous carbon content than other test fuels. The D and G peak positions of different soot samples
255
shifted slightly due to the changes of different combustion products from C-H and C-C. The larger D3
256
band area and smaller D1 band area corresponding to RP-3 indicated that the samples of the traditional
257
fuels had more amorphous carbon and less defects at the graphene layer edges than the samples of the
258
alternative aviation fuels at 2 bar. However, at 8 bar, the samples of the alternative fuels showed less
259
defects at the graphene layer edges and more graphitic crystal (smaller D1 band area and larger G band
260
area) compared with kerosene.
14 / 21
ACS Paragon Plus Environment
Page 15 of 21
Environmental Science & Technology
261 262
Figure 8. Relative intensity and the full width at half maximum (FWHM) obtained from Raman spectra: (a)
263
ID1/IG, (b) D1 FWHM, (c) ID2/IG, (d) ID3/IG.
264
The intensity ratio between D1 and G (ID1/IG) manifests the graphitic crystalline degree of the
265
sample particles, and smaller ID1/IG means that carbon layer has higher structural order of graphitic
266
crystalline 46. Figure 8(a) showed the variation in the ratio ID1/IG of the soot emissions of different fuels
267
at 2 bar and 8 bar BMEP. As the BMEP increased, the average ratio ID1/IG of RP-3 and R80P20
268
particles declined by 20% and 7%, respectively, and the average ratio ID1/IG of R60P40 increased by
269
32%. R60P40 particles had the highest degree of graphitization with the lowest ratio of ID1/IG at 2 bar,
270
while R75F25 particles had the highest degree of graphitization at 8 bar. The mean ID1/IG ratios of all
271
fuels were greater than unity. During the conversion process from amorphous carbon to ideal graphitic
272
lattice, ID1/IG increases initially and then declines 54. Since soot emissions contained much amorphous
273
carbon, the ID1/IG variation were different for soot samples with varying graphitization degrees.
274
Moreover, the ratio ID1/IG could also be used to estimate the fringe length which was proportional to
275
ID1/IG 55.
276
From Table 2 and Figure 8(a), one could conclude that R80P20 particles at 8 bar had the highest 15 / 21
ACS Paragon Plus Environment
Environmental Science & Technology
Page 16 of 21
277
defective structure with the lowest degree of graphitization. In general, the Raman spectra were in
278
agreement with the analysis of nano-structure obtained from HRTEM images.
279
Figure 8(b) illustrates the full width at half maximum of D1 (D1 FWHM) of soot samples. Higher
280
D1 FWHM implied higher levels of chemical heterogeneity and lower degree of crystal structure order
281
56.
282
2 bar to 8 bar which could be attributed to the fact that complete combustion at high engine load
283
resulted in the decrease of intermediate products 57, indicating lower levels of chemical heterogeneity,
284
i.e. the average chemical composition of the copolymer as the function of the molar mass
285
BMEP samples with high degree of graphitic order could be attributed to charring effects which
286
convert organic molecules of high molecular mass into disordered graphite-like structures (charcoal)
287
57.
288
surface which mitigated the oxidation of the ‘core’ soot.
289
The mean D1 FWHM of all alternative fuels soot samples decreased as the BMEP increased from
58.
High
Under low BMEP conditions, there are abundant unburned fuel organic species attached to soot
ID2/IG reflected surface area-to-volume ratio of graphitic crystals, which indicated that ID2/IG could 59.
290
be treated as inversely proportional to the thickness of graphitic crystallites
Figure 8(c)
291
demonstrates that R75F25 and R60P40 particles had higher ID2/IG than other sample particles,
292
suggesting that they had thinner graphitic crystallites than the other sample particles. Thinner graphitic
293
crystallites featured more oxidant activities because high porosity could increase the oxide bonding in
294
graphene layers 57.
295
The origins of D3 band are related to amorphous carbon, and ID3/IG reflects the fraction of the
296
amorphous carbon in soot samples. The mean intensity ratio ID3/IG of RP-3 (0.75) was greater than that
297
of diesel (0.20) at 2 bar as shown in Figure 8(d). Furthermore, the mean intensity ratios ID3/IG of
298
R80P20, R60P40 and R75F25 particles were similar at 8 bar BMEP, yet exhibited large variation at 2
299
bar BMEP. The decrease in ID3/IG (except diesel) implied more ordered crystallite arrangement with 16 / 21
ACS Paragon Plus Environment
Page 17 of 21
300
Environmental Science & Technology
gradual oxidation of oxygen functional groups (alcohol group) 29.
301
Pentanol addition decreased the combustion duration and protracted ignition delay due to the lower
302
energy density of pentanol compared with the hydrocarbon fuels, which lead to the particles had the
303
highest defective structure with the lowest degree of graphitization. As the BMEP increased, RP-3
304
decreased the degree of graphitization because of its low cetane number and high volatility. The
305
particle oxidation reactivity seemed to be strongly dependent on fuel type and noticeably distinct
306
Raman spectra were observed for different test fuels. Using alternative aviation fuels in APEs,
307
especially adding higher alcohols would alter soot molecular structure and corresponding soot
308
oxidative reactivity, which has consequences for ice nucleation, haze formation and global climate
309
pattern. It is desirable to evaluate the oxidation reactivity of particles emitted from aircraft engines
310
burning alternative aviation fuels in order to comprehensively understand their environmental
311
implications.
312
313
Supplemental information
ASSOCIATED CONTENT
314
The supplemental information is related to this article. Table S1 gives the engine specifications.
315
Figure S1 illustrates the layout of the research engine test rig. Figure S2 lists HRTEM images of
316
representative soot particles. Figure S3 illustrates typical first-order Raman spectra of ten PM samples
317
using the embedded ‘Lebspec5’ software. Figure S4 shows typical Raman spectrum curves for the PM
318
samples from different fuels. Figure S5 shows the Raman spectrum of the quartz filter which was
319
subtracted in pretreatment.
320
AUTHOR INFORMATION
17 / 21
ACS Paragon Plus Environment
Environmental Science & Technology
Page 18 of 21
321
Corresponding Author
322
*Tel: +41 44 633 36 21, E-mail:
[email protected] 323
ORCID
324
Jing Wang: 0000-0003-2078-137X
325
Notes
326
The authors declare no competing financial interest.
327
328
This work is funded by National Natural Science Foundation of China (Grants No. 9164119).
329
REFERENCES
330 331 332 333 334 335 336 337 338 339 340 341 342 343 344 345 346 347 348 349 350 351 352 353 354
1.
Masiol, M.; Harrison, R. M., Aircraft engine exhaust emissions and other airport-related contributions to ambient air
ACKNOWLEDGEMENTS
pollution: A review. Atmos. Environ. 2014, 95 (1), 409-455. 2.
Woody, M. C.; Arunachalam, S., Secondary organic aerosol produced from aircraft emissions at the Atlanta Airport:
An advanced diagnostic investigation using process analysis. Atmospheric Environment 2013, 79, 101-109. 3.
Stettler, M. E. J.; Boies, A. M.; Petzold, A.; Barrett, S. R. H., Global Civil Aviation Black Carbon Emissions.
Environmental Science & Technology 2013, 47 (18), 10397-10404. 4.
Lee, D. S.; Fahey, D. W.; Forster, P. M.; Newton, P. J.; Wit, R. C. N.; Lim, L. L.; Owen, B.; Sausen, R., Aviation and
global climate change in the 21st century. Atmos. Environ. 2009, 43 (22), 3520-3537. 5.
Lee, D. S.; Pitari, G.; Grewe, V.; Gierens, K.; Penner, J. E.; Petzold, A.; Prather, M. J.; Schumann, U.; Bais, A.;
Berntsen, T., Transport impacts on atmosphere and climate: Aviation. Atmos. Environ. 2010, 44 (37), 4678-4734. 6.
FAA. https://www.faa.gov/data_research/aviation_data_statistics/general_aviation/CY2016/.
7.
GAMA. https://gama.aero/facts-and-statistics/statistical-databook-and-industry-outlook/.
8.
Board, T. R.; National Academies of Sciences, E.; Medicine, Exhaust Emissions from In-Use General Aviation
Aircraft. The National Academies Press: Washington, DC, 2016; p 122. 9.
Bolaños Alomía, A. M.; Merchancano Rosero, J. D.; Arcila González, M. B.; Yepes Chamorro, B. In Gaseous and
Particulate Emissions Results of the NASA Alternative Aviation Fuel Experiment (AAFEX), ASME Turbo Expo 2010: Power for Land, Sea, and Air, 2010; pp 1195-1207. 10. https://www.icao.int/environmental-protection/Pages/technology-standards.aspx. 11. Depcik, C., Performance and Emissions Characteristics of Hydroprocessed Renewable Jet Fuel Blends in a SingleCylinder Compression Ignition Engine with Electronically Controlled Fuel Injection. Combustion Science & Technology 2015, 187 (6), 857-873. 12. Arkoudeas, P.; Kalligeros, S.; Zannikos, F.; Anastopoulos, G.; Karonis, D.; Korres, D.; Lois, E., Study of using JP-8 aviation fuel and biodiesel in CI engines. Energy Conversion & Management 2003, 44 (7), 1013-1025. 13. Rye, L.; Blakey, S.; Wilson, C. W., Sustainability of supply or the planet: a review of potential drop-in alternative aviation fuels. Energy & Environmental Science 2010, 3 (1), 17-27. 18 / 21
ACS Paragon Plus Environment
Page 19 of 21
355 356 357 358 359 360 361 362 363 364 365 366 367 368 369 370 371 372 373 374 375 376 377 378 379 380 381 382 383 384 385 386 387 388 389 390 391 392 393 394 395 396 397 398 399 400
Environmental Science & Technology
14. Bruno, T. J.; Baibourine, E., Comparison of Biomass-Derived Turbine Fuels with the Composition-Explicit Distillation Curve Method. Energy & Fuels 2011, 25 (4), 1847-1858. 15. Schripp, T.; Anderson, B.; Crosbie, E. C.; Moore, R. H.; Herrmann, F.; Oßwald, P.; Wahl, C.; Kapernaum, M.; Köhler, M.; Le Clercq, P.; Rauch, B.; Eichler, P.; Mikoviny, T.; Wisthaler, A., Impact of Alternative Jet Fuels on Engine Exhaust Composition During the 2015 ECLIF Ground-Based Measurements Campaign. Environmental Science & Technology 2018, 52 (8), 4969-4978. 16. Rajasekar, E.; Murugesan, A.; Subramanian, R.; Nedunchezhian, N., Review of NOx reduction technologies in CI engines fuelled with oxygenated biomass fuels. Renewable & Sustainable Energy Reviews 2010, 14 (7), 2113-2121. 17. Raganati, F.; Olivieri, G.; Götz, P.; Marzocchella, A.; Salatino, P., Butanol Production from Lignocellulosic-based Hexoses and Pentoses by Fermentation of Clostridium Acetobutylicum. Anaerobe 2012, 34. 18. Petranović, Z.; Bešenić, T.; Vujanović, M.; Duić, N., Modelling pollutant emissions in diesel engines, influence of biofuel on pollutant formation. Journal of Environmental Management 2017, 1038-1046. 19. Dagaut, P.; Cathonnet, M., The ignition, oxidation, and combustion of kerosene: A review of experimental and kinetic modeling. Progress in Energy and Combustion Science 2006, 32 (1), 48-92. 20. Wang, H. R., Preliminary investigation on detailed chemical reaction mechansim of RP-3 aviation kerosene. Gas Turbine Experiment & Research 2015. 21. Parent, P.; Laffon, C.; Marhaba, I.; Ferry, D.; Regier, T. Z.; Ortega, I. K.; Chazallon, B.; Carpentier, Y.; Focsa, C., Nanoscale characterization of aircraft soot: A high-resolution transmission electron microscopy, Raman spectroscopy, Xray photoelectron and near-edge X-ray absorption spectroscopy study. Carbon 2016, 101, 86-100. 22. Wei, J.; Song, C.; Lv, G.; Song, J.; Wang, L.; Pang, H., A comparative study of the physical properties of in-cylinder soot generated from the combustion of n -heptane and toluene/ n -heptane in a diesel engine. Proceedings of the Combustion Institute 2015, 35 (2), 1939-1946. 23. Zhang, D.; Ma, Y.; Zhu, M., Nanostructure and oxidative properties of soot from a compression ignition engine: The effect of a homogeneous combustion catalyst. Proceedings of the Combustion Institute 2013, 34 (1), 1869-1876. 24. Beyssac, O.; Goffé, B.; Petitet, J. P.; Froigneux, E.; Moreau, M.; Rouzaud, J. N., On the characterization of disordered and heterogeneous carbonaceous materials by Raman spectroscopy. Spectrochim Acta A Mol Biomol Spectrosc 2003, 59 (10), 2267-76. 25. Knauer, M.; Schuster, M. E.; Su, D.; Schlögl, R.; Niessner, R.; Ivleva, N. P., Soot structure and reactivity analysis by Raman microspectroscopy, temperature-programmed oxidation, and high-resolution transmission electron microscopy. Journal of Physical Chemistry A 2009, 113 (50), 13871-80. 26. Liati, A.; Eggenschwiler, P. D.; Schreiber, D.; Zelenay, V.; Ammann, M., Variations in diesel soot reactivity along the exhaust after-treatment system, based on the morphology and nanostructure of primary soot particles. Combustion & Flame 2013, 160 (3), 671-681. 27. Wal, R. L. V.; Tomasek, A. J., Soot oxidation : dependence upon initial nanostructure. Combustion & Flame 2003, 134 (1), 1-9. 28. Saffaripour, M.; Tay, L. L.; Thomson, K. A.; Smallwood, G. J.; Brem, B. T.; Durdina, L.; Johnson, M., Raman spectroscopy and TEM characterization of solid particulate matter emitted from soot generators and aircraft turbine engines. Aerosol Science & Technology 2017, 51 (4), 518-531. 29. Wang, Y.; Liang, X.; Tang, G.; Chen, Y.; Dong, L.; Shu, G., Impact of lubricating oil combustion on nanostructure, composition and graphitization of diesel particles. Fuel 2016, 237-244. 30. Liati, A.; Brem, B. T.; Durdina, L.; Vögtli, M.; Dasilva, Y. A. R.; Wang, J., Electron Microscopic Study of Soot Particulate Matter Emissions from Aircraft Turbine Engines. Environmental Science & Technology 2014, 48 (18), 1097510983. 31. Atmanli, A.; Ileri, E.; Yuksel, B.; Yilmaz, N., Extensive analyses of diesel-vegetable oil-n-butanol ternary blends in a diesel engine. Applied Energy 2015, 145, 155-162. 32. Kalghatgi, G. T., Auto-Ignition Quality of Practical Fuels and Implications for Fuel Requirements of Future SI and 19 / 21
ACS Paragon Plus Environment
Environmental Science & Technology
401 402 403 404 405 406 407 408 409 410 411 412 413 414 415 416 417 418 419 420 421 422 423 424 425 426 427 428 429 430 431 432 433 434 435 436 437 438 439 440 441 442 443 444 445 446
Page 20 of 21
HCCI Engines. Society of Automotive Engineers Sae 2005, 26 (4), 41-53. 33. Sadezky, A.; Muckenhuber, H.; Grothe, H.; Niessner, R.; Pöschl, U., Raman microspectroscopy of soot and related carbonaceous materials: Spectral analysis and structural information. Carbon 2005, 43 (8), 1731-1742. 34. Dresselhaus, M. S.; Dresselhaus, G., Light scattering in graphite intercalation compounds. Springer Berlin Heidelberg: 1976; p 3-57. 35. Bacsa, W. S.; Lannin, J. S.; Pappas, D. L.; Cuomo, J. J., Raman scattering of laser-deposited amorphous carbon. Physical Review B Condensed Matter 1993, 47 (16), 10931-10934. 36. Shirakawa, H.; Ito, T.; Ikeda, S., Raman Scattering and Electronic Spectra of Poly(acetylene). Polymer Journal 1973, 4 (4), 460-462. 37. Yehliu, K.; Wal, R. L. V.; Boehman, A. L., Development of an HRTEM image analysis method to quantify carbon nanostructure. Combustion & Flame 2011, 158 (9), 1837-1851. 38. Wal, R. L. V., Soot nanostructure: Definition, quantification and implications. Sae Transactions 2005, 114, 429-436. 39. Jung, H.; Kittelson, D. B.; Zachariah, M. R., Kinetics and visualization of soot oxidation using transmission electron microscopy. Combustion & Flame 2004, 136 (4), 445-456. 40. Dan, B.; Anderson, B.; Wey, C.; Howard, R.; Winstead, E.; Beyersdorf, A.; Corporan, E.; Dewitt, M. J.; Klingshirn, C.; Herndon, S. In Gaseous and Particulate Emissions Results of the NASA Alternative Aviation Fuel Experiment (AAFEX), ASME Turbo Expo 2010: Power for Land, Sea, and Air, 2010; pp 1195-1207. 41. Christie, S.; Lobo, P.; Lee, D.; Raper, D., Gas Turbine Engine Nonvolatile Particulate Matter Mass Emissions: Correlation with Smoke Number for Conventional and Alternative Fuel Blends. Environmental Science & Technology 2017, 51 (2), 988-996. 42. Christie, S.; Raper, D.; Lee, D. S.; Williams, P. I.; Rye, L.; Blakey, S.; Wilson, C. W.; Lobo, P.; Hagen, D.; Whitefield, P. D., Polycyclic Aromatic Hydrocarbon Emissions from the Combustion of Alternative Fuels in a Gas Turbine Engine. Environmental Science & Technology 2012, 46 (11), 6393-6400. 43. Fayad, M. A.; Herreros, J. M.; Martos, F. J.; Tsolakis, A., Role of Alternative Fuels on Particulate Matter (PM) Characteristics and Influence of the Diesel Oxidation Catalyst. Environmental Science & Technology 2015, 49 (19), 1196711973. 44. Clague, A. D. H.; Donnet, J. B.; Wang, T. K.; Peng, J. C. M., A comparison of diesel engine soot with carbon black 1. Carbon 1999, 37 (10), 1553-1565. 45. Zhang, R.; Kook, S., Structural evolution of soot particles during diesel combustion in a single-cylinder light-duty engine. Combustion & Flame 2015, 162 (6), 2720-2728. 46. Agudelo, J. R.; Álvarez, A.; Armas, O., Impact of crude vegetable oils on the oxidation reactivity and nanostructure of diesel particulate matter. Combustion & Flame 2014, 161 (11), 2904-2915. 47. Toth, P.; Palotas, A. B.; Ring, T. A.; Eddings, E. G.; Wal, R. V.; Lighty, J. A. S., The effect of oxidation pressure on the equilibrium nanostructure of soot particles. Combustion & Flame 2015, 162 (6), 2422-2430. 48. Zhang, Y.; Zhang, R.; Rao, L.; Kook, S. In A Comparison between In-Flame and Exhaust Soot Nanostructures in a Light-Duty Diesel Engine, WCX™ 17: SAE World Congress Experience, 2017. 49. Kroto, H. W.; Heath, J. R.; O'Brien, S. C.; Curl, R. F.; Smalley, R. E., C60: Buckminsterfullerene. Nature 1985, 318 (6042), 162-163. 50. Dresselhaus, M. S.; Dresselhaus, G.; Eklund, P. C., Chapter 20–Applications of Carbon Nanostructures. Science of Fullerenes & Carbon Nanotubes 1996, 870-917. 51. Ebbesen, T. W., Carbon nanotubes : preparation and properties / edited by Thomas W. Ebbesen. American Journal of Transplantation Official Journal of the American Society of Transplantation & the American Society of Transplant Surgeons 1996, 12 (3), 545–553. 52. Wal, R. L. V.; Yezerets, A.; Currier, N. W.; Kim, D. H.; Wang, C. M., HRTEM Study of diesel soot collected from diesel particulate filters. Carbon 2007, 45 (1), 70-77. 53. Sharma, V.; Bagi, S.; Patel, M. K.; Adeniran, O.; Aswath, P. B., Influence of Engine Age on Morphology and 20 / 21
ACS Paragon Plus Environment
Page 21 of 21
447 448 449 450 451 452 453 454 455 456 457 458 459 460
Environmental Science & Technology
Chemistry of Diesel Soot Extracted from Crankcase Oil. Energy & Fuels 2016, 30 (3), 2276–2284. 54. Ferrari, A. C.; Robertson, J., Interpretation of Raman spectra of disordered and amorphous carbon. Phys.rev.b 2000, 61 (20), 14095-14107. 55. Ferrari, A. C.; Basko, D. M., Raman spectroscopy as a versatile tool for studying the properties of graphene. Nature Nanotechnology 2013, 8 (4), 235-46. 56. Knauer, M.; Carrara, M.; Rothe, D.; Niessner, R.; Ivleva, N. P., Changes in Structure and Reactivity of Soot during Oxidation and Gasification by Oxygen, Studied by Micro-Raman Spectroscopy and Temperature Programmed Oxidation. Aerosol Science and Technology 2009, 43 (1), 1-8. 57. Ivleva, N. P.; McKeon, U.; Niessner, R.; Pöschl, U., Raman Microspectroscopic Analysis of Size-Resolved Atmospheric Aerosol Particle Samples Collected with an ELPI: Soot, Humic-Like Substances, and Inorganic Compounds. Aerosol Science & Technology 2007, 41 (7), 655-671. 58. Yau, W. W.; Kirkland, J. J.; Bly, D. D., Modern size-exclusion liquid chromatography. Wiley: 1979; p 1–6. 59. Sze, S. K.; Siddique, N.; Sloan, J. J.; Escribano, R., Raman spectroscopic characterization of carbonaceous aerosols. Atmos. Environ. 2001, 35 (3), 561-568.
461
21 / 21
ACS Paragon Plus Environment