Journal of Chemistry

Journal of Chemistry / 2013 / Article

Research Article | Open Access

Volume 2013 |Article ID 528471 |

Małgorzata Szewczyńska, Małgorzata Pośniak, Elżbieta Dobrzyńska, "Study on Individual PAHs Content in Ultrafine Particles from Solid Fractions of Diesel and Biodiesel Exhaust Fumes", Journal of Chemistry, vol. 2013, Article ID 528471, 10 pages, 2013.

Study on Individual PAHs Content in Ultrafine Particles from Solid Fractions of Diesel and Biodiesel Exhaust Fumes

Academic Editor: Jean-Luc Blin
Received05 Jun 2012
Revised30 Jul 2012
Accepted04 Aug 2012
Published02 Oct 2012


In order to characterize PAHs emissions of diesel engine fuelled with diesel and its blend (B20, B40). In the particle phase, PAHs in engine exhausts were collected by fiberglass filters using Electrical Low Pressure Impactor (ELPI) and then determined by a high performance liquid chromatography with a fluorimetric detector (HPLC-FL). The main content in exhaust gases from diesel engine, regardless the type of applied fuel, is constituted by the particles fraction of diameter <0.25 μm. Particles sized <0.25 μm constituted on average approximately 68% of particles in diesel exhaust gases and approx. 50% of particles emitted by biodiesel B20 and B40. When the B100 bioester additive was applied, the total emission of particles was reduced thus the volume of toxic substances adsorbed on them was lower. The analysis of chemical composition of <0.25 μm exhaust gas fraction showed that there were mainly 3- and 4-ring aromatic hydrocarbons in the exhaust gas of diesel fuel while in B40 single PAHs with the number of rings of 4 and 5 were detected. An application of ELPI permitted a further separation of <0.25 μm particle’s fraction and a real-time determination of interalia number, mass, and surface concentrations.

1. Introduction

In an atmospheric air and in the air surrounding people in work and life premises, there are particles which may have a negative impact on human health. One of the most important sources of factors dangerous to health are diesel engine exhaust fumes, that is, mixtures of chemical compounds created as a result of incomplete combustion of diesel fuel and engine oil, as well as modifiers and contaminants contained in them. These undesired combustion products are emitted to the atmosphere in the form of particulates of various sizes and shapes, and in the form of gases and vapours.

Diesel engine exhaust emissions are of a major interest to researchers at national and international levels as demonstrated both by numerous publications resulting from analyses of gas and particular phase, evaluations of occupational and environmental exposure, and toxicological and epidemiological studies, and by reviewing publications indicating directions for further research in the area [13]. The publications are concerned mainly on exhaust gases emitted during combustion of conventional fuels. With reference to the necessity to reduce the emission of contaminations from internal-combustion engines, the growing worldwide interest regarding the application of environment-friendly fuels is observed. In many countries, studies are conducted with a view to replace a conventional fuel (petrodiesel) with alternative fuels, such as biodiesel and ethanol [46]. At the same time a question arises whether alternative fuels bring about benefits only or may also induce unfavourable effects on environment and human health, similar to the effects caused by multicompound mixtures of harmful xenobiotics created as a result of combustion of conventional fuels (e.g., carcinogenic, mutagenic and fertility impairing ones), emitted to the environment both in a gas phase and in the form of fine and ultrafine particles [79].

However, the literature data indicates that particulate matter (PM) is currently the most serious air contaminant causing nearly 300,000 deaths every year in Europe. Epidemiological examinations indicate that the growth of PM concentrations leads to diseases of respiratory and cardiovascular system and even to deaths [10, 11]. Fine PM particles (dp < 2.5 μm) cause pneumonia and systemic health effects [12].

Contrary to the behaviour of inhaled PM10 and PM2.5, ultrafine particles deposited in lungs have the ability to penetrate tissue and undergo interstitialization as well as to be absorbed directly into the bloodstream. Therefore, they are not easily removed from the body and may have immediate effect. An exposure to ultafine particles, even if components are not very toxic, may cause oxidative stress, inflammatory mediator release, and induce lung disease and other systemic effects [13, 14]. Moreover, conducted studies [15] indicate that employees exposed to this type of PM suffer fairly more often from neoplastic diseases. The carcinogenic process under the influence of PM, and especially ultrafine fractions (dp < 2.5 μm) containing mixtures of xenobiotics, has not been fully investigated yet.

Studies published up to now concerning exhaust fumes originating from biofuels do not strictly confirm the reduction of harmful xenobiotics emission in comparison with conventional fuel [1621]. Diverse point of views on emission of particles originating from petro- and biodiesel fuel are presented in the literature, especially on forming of fine particles, including nanoparticles [22, 23]. Some scientists claim that PM emission of particles from biodiesel increases compared to conventional fuel while others observe only slight changes. One study indicates that adding 20% of biofuel to conventional fuel in diesel engines induced a reduction of PM emission by 16–33%, carbon dioxide by 11–25%, and hydrocarbons by 19–32% in total. [24] Studies of Westphal et al. [25] show that the use of cold-pressed rapeseed oil as a fuel results in an increased emission of mutagenic compounds compared to the reference diesel fuel. However, the studies carried out up to now are insufficient to draw unequivocal conclusions.

Harmful effects caused by the particulates matter, are chemical composition dependant. The published data suggests that, due to the adsorption or condensation phenomena, significant amounts of gases or volatile organic substances may sediment on solid particles and in such combinations may penetrate respiratory tracts of workers. Toxic effects of dusts depend on diameter of comprising particles. The ability of fine particles (of diameters (dp) smaller than 2.5 μm) to penetrate lung airways and gas-exchange regions results in considerably higher bioavailability of enclosed chemical substances than the bioavailability of substances present in larger particles. However, recognition of a toxic activity of very fine dust fractions (smaller than 2.5 μm) is so far incomplete.

Polycyclic aromatic hydrocarbons (PAHs) are widespread contaminants which can be deposited onto particles formed during an incomplete combustion of organic matter in the presence of air. Since several PAHs and some of their degradation products (oxygenated and nitrated PAHs) are known to have high carcinogenic and mutagenic potential [26], they have been consequently included in the European Union priority lists of pollutants [27, 28]. Benzo(a)pyrene (a 5-ring PAH), considered one of the most carcinogenic PAHs, has been used as an indicator of environmental PAH exposures.

The review of the topic literature points to the existing gaps in research on composition of ultrafine particles originating from combustion of both types of fuel.

Therefore, this paper focuses on the use of low-pressure cascade impactor (Electrical Low Pressure Impactor ELPI) for the separation of individual fractions of fine particles of diesel exhaust gases resulting from a combustion of biofuels and aims to investigate the content of polycyclic aromatic hydrocarbons (PAHs).

2. Materials and Methods

2.1. Chemicals and Materials

A standard PAHs mixture and corresponding individual compounds were obtained from Supelco. The standard PAHs mixture (EPA 610 Polynuclear Aromatic Hydrocarbons Mix 100–2000 μg mL−1 MEOH : CH2Cl2(1 : 1)) contains: naphthalene (NA), acenaphtene (AC), fluorene (FL), phenanthrene (PH), anthracene (AN), fluoranthene (FLR), pyrene (PY), benzo(a)anthracene (BaA): chrysene (CH), benzo(b)fluoranthene (BbF), benzo(k)fluoranthene (BkF), dibenzo(ah)anthracene (DBA) and benzo(a)pyrene (BaP), benzo(ghi)perylene (BghiP), and indeno(1,2,3-cd)pyrene (IN).

Acetonitrile, dichloromethane, and methanol were of analytical grade and were purchased from Sigma-Aldrich. Iso-propanol was purchased from J. T. Baker (Deventer, Netherlands). Milli-Q water, obtained with a Milli-Q system (Millipore, Bedford, MA, USA), was used for analysis. Sigma-Aldrich SPE 12 vacuum system (Visiprep SPE Vacuum Manifold) was used for extraction. Bakerbond PolarPlus columns were purchased at J. T. Baker (Deventer, The Netherlands).

2.2. Sampling Site

The test stand used for generation and studies of diesel and biodiesel exhausts was prepared in a garage of ca. 5 × 4 m in size. For the presented studies, a diesel common rail engine system (from the car Skoda Fabia) of 2.0 L volumetric capacity with 130 kW of power at 1,400 rpm manufactured in 2007 was used. The engine was mounted on a portable trolley (Figure 1). A commercial EKODIESEL PLUS 50 (by Polish Oil Concern ORLEN, Poland) of cetane number not smaller than 51, density of 820–845 g m−3 and the sulphur content not higher than 50 mg kg−1 was used as a diesel fuel and a commercial Bioester 100 (by Refinery Trzebinia, Group ORLEN, Poland) was a biofuel derived from plant oils. Three types of fuel were preparthed in laboratory and used in this study: ON (100% diesel), B20 (20% bioester B100, and 80% ON), B40 (40% bioester B100 + 60% ON). Fuel and biofuel properties are given in Table 1.


AppearanceYellow liquid
Boiling point 347°C
The temperature of freezing °C
Flash pointNot less than 120°C
Ignition temperatureUnder 250°C
Limit of explosivenessThe product does not pose a risk of explosion
Vapour pressure in temp. 50°C: < 1 kPa
Density (6)0.860 ÷ 0.900 g cm−3
Kinetic viscosity (20)3.5–5 mm2 s−1
SolubilityInsoluble in water; soluble in most organic solvents
Heat of combustionca. 40 190 kJ/kg


Fatty acid (Rapeseed) Methyl Esters (RME) content 96.5% (by mass)
Density at 15°C max. 900 kg/m3
Viscosity at 40°C max 5.00 mm2/s
Flash point 101°C
Cetane number 51.0
Specific energy 37.7 MJ/kg

2.3. PAHs Sampling and Analysis

PAHs samples of particle-phase were collected by using a PAHs sampling system ELPI (Dekati, Finland) at a temperature below 52°C for 7 days for 5-6 hours at the flow rate of 30 L min−1. About 9,000–10,800 L of air was passed through the ELPI sampler every day.

Basic parameters of ELPI operations are presented below.impactor output pressure: 100 m bar,impactor input pressure: 1013 m bar,flow: 30 L min−1,charging voltage (U): 5 kV,charging current (I): 1 μA,correlation coefficient: enabled,type of particle diameter: aerodynamic.

Sampled gas was drawn from the tailpipe and diluted in an ejection double dilutor (Dekati, Finland) enabling to control the dilution ratio around 64. The engine was lunched 15 min before collecting particle-phase PAHs with fuel corresponding to the cycle of measurements. Particle-phase PAHs were collected on fiberglass filters weighed on an analytical electronic balance (Mettler Toledo AT261, Switzerland) before and after each collection. Before each weighting the filters were preconditioned in a desiccator for 10 h to remove moisture. The samples were stored in a refrigerator at 4°C for less than 7 days until extraction.

PAHs were extracted from filters with 10 mL dichloromethane. A sonic bath was also used with closed vials for 30 min in ice to prevent losses by volatilization. SPE method with a BakerBond PolarPlus column and a mixture of acetonitrile/isopropanol (1 : 1, v : v) was applied in order to clean samples before further HPLC analysis.

Separation and identification of the PAHs were achieved by using HPLC (EliteLaChrom, Merck Hitachi) with fluorescence detection (FL) in accordance with methods described in the standard PN-Z-04240-5 2006. [29] A reversed phase HPLC column (Pinnacle II PAH, 150 × 32 mm, 5 μm particle size) by Restek was used with a pre-column (20 3.2 mm). The flow rate was 0.97 mL min−1 and the injection volume was 10 μL. Elution was performed with a gradient starting from an eluent composition of 50% acetonitrile in water (up to 5 min). The acetonitrile concentration was increased up to 100% in 25 min and maintained at 100% for 5 min. The wavelength of the fluorescence detector was altered for each PAHs [30]. The data was collected and processed with HP ChemStation software. LOD results for selected PAHs, determined based on blank analysis, did not exceed 0.1 ng m−3.

3. Results and Discussion

Concentrations and Size Distributions of Particles Emitted from Diesel Engine Exhaust Fumes. A subject to observation during real-time measurements was a distribution of particles for respective fractions emitted from diesel engine operating with the use of various biofuel mixtures for 2 to 5 hours on average. During real-time measurements with the use of ELPI the data was collected concerning changes in composition of fractions. The data was registered each 10 seconds. After ceasing the engine operations, the data was computed and processed with the use of ELPIVI 4.0 software and then, thanks to ELPIxls tab, transferred to Excel and saved in the form of calculation worksheets and charts.

Examples of histograms of particle distribution obtained during one measurement day for ON and B40 fuels are presented in Figure 2.

An analysis of an exemplary data presented in Figure 2 for number concentration distribution over one measurement day confirms a particle emission reduction obtained for B40 by 70% when compared to ON.

Similarly, when examining mean values of number, diameter and mass concentration distribution, a reduction of total particle emission is observed, respectively, by 54% (B20) and 78% (B40), 32% (B20) and 88% (B40), and 47% (B20) and 69% (B40) compared to the values obtained for ON (Figure 3).

After analyzing the obtained results, an observation arises as the main contents of diesel engine exhausts are constituted by fraction of dp < 0.25 μm which is probably connected with the manner of sampling. In this study, samples were taken directly from the engine exhaust while an exhaust gas temperature was high. As the size of particulates grows with the decrease of exhaust gas temperature, for high temperatures (>160°C) of exhaust gases particles of size lower than 1 μm constitute approximately 96% of the total emission mass while in low temperatures (<110°C) the amount drops. It is assumed that with a decrease of a temperature to approx. 119–159°C, a rapid growth of the number of bigger particles occurs (98/83/EC).

3.1. Gravimetric Determination of Mass Concentration of Exhaust Gas Fractions

In order to determine a mass concentration for respective fractions of dust emitted from diesel engine exhaust gases before analyzing a chemical composition of diesel gas particles separated on ELPI collecting plates, filters collecting respective fractions were weighed with a use of an ultrabalance. The results of examination of mass concentration of diesel engine exhaust gas particulates, operated with the use of biofuel mixtures, are presented in Table 2.

EPLI ( )*
StorageD50% [ m]Diesel ONB20B40
Mass concentration [mg m−3]

Filter no.0.0072.7162.2670.043

Total mass concentration for fraction < 0.25  m 13.8763.7381.954
Total mass concentration 23.6058.2905.148

The analysis of a distribution of mass concentrations for respective fractions of particles emitted from the exhaust fumes (with a dedicated use of Electrical Low Pressure Impactor (ELPI) for which it was possible to determine fractions of diameter from 10 μm to below 0.03 μm) indicates a decrease in mass concentration of particles diameter below 1 μm along with the increase of B100 bioester contents in the biofuel mixture (Figure 4).

With application of B40 mixture, the reduction of particles emission of dp below 1 μm totals on average approximately 80% compared to pure diesel fuel (ON), similar to real-time observation of particle distribution with the use of ELPI for which the obtained average value of reduction of total mass concentration of particles amounts to nearly 70%.

3.2. Particle Fractions of Polycyclic Aromatic Hydrocarbons in diesel Engine Exhaust Gas

A determination of polycyclic aromatic hydrocarbons (PAHs) in individual fractions of diesel exhaust fumes required a collection of adequate mass of material (dust) for an examination. The use of ELPI impactor to examine the chemical composition of respective fractions in the range from 10 μm to 0.03 μm and a system of 64-fold dilution of the collected fumes enables an idetification of PAHs deposited on separated dust fractions.

Table 3 presents the PAHs identified in respective fractions of diesel engine exhausts fractions with the use of ELPI.

StorageD50% [ m]Diesel ONB20B40
Results of PAHs identification

10.03AC, FL, BaA, CH
BkF, BghiP
20.06AC, FL
BaA, CH, BkF
FL, BkF, BghiPPY, CH, BkF
30.108AC, FL
BkF, BghiP
BkF, BaP
BkF, BaP
40.17NA, PH
BkF, DBA, BghiP
DBA, BghiP
50.26NA, AC
DBA, BghiP
DBA, BghiP
60.40PY, BaA
CH, BkF, BaP
DBaA, BghiP
70.65NA, AC, FL, PH
FL, BaA, CH, BkF
DBA, BghiP
81.0NA, AC, FL, PH
Not found
114.4Not found

Naphthalene (NA); acenaphtene (AC), fluorene (FL), phenanthrene (PH), anthracene (AN); fluoranthene (FLR), pyrene (PY), benzo(a)anthracene (BaA): chrysene (CH), benzo(b)fluoranthene (BbF), benzo(k)fluoranthene (BkF), dibenzo(ah)anthracene (DBA) and benzo(a)pyrene (BaP), benzo(ghi)perylene (BghiP) and indeno(1,2,3-cd)pyrene (IN).

However, an insufficient mass of diesel exhaust particles in particles fractions of diameters from 1.6 μm to 10 μm and in 0.007 μm made the analysis of their chemical composition impossible. In other fractions, the highest volume of PAHs was identified in ON fumes. While in exhaust fumes of 100% ON fuel mainly 3- and 4-ring aromatic hydrocarbons occured, in B40 mixture single hydrocarbons with 4 and 5 rings were identified. The identification data of individual PAHs obtained in separated fractions could be compared with the results published in the work of Corrêa and Arbilla [24], in which the gaseous and solid PAHs phase was determined in diesel fumes (ON), and in B2, B5, and B20 mixtures. The authors collected air samples on Teflon filters and XAD-2 and confirmed the occurrence in the examined exhaust gases of mostly 3-and 4-ring hydrocarbons, including firstly phenanthrene, fluorene, naphthalene, acenaphthalene, acenaphtylene, and anthracene.

In Table 4 the results of quantitative PAHs analysis in fraction of dp < 0.25 μm are presented. The data indicates that the summary contents of PAHs in ON fumes was on average 910 ng m−3 and decreased with B100 bioester addition to diesel fuel mixture. In B40 exhaust fumes the average summary contents of PAHs was 340 ng m−3 signifying a reduction of PAHs in the fumes by 62% when compared to the emission of the compounds during diesel fuel combustion.

100% ONB20B40
PAHMinMaxAverageSDRSD [%]MinMaxAverageSDRSD [%]MinMaxAverageSDRSD [%]
ng m−3ng m−3ng m−3ng m−3ng m−3ng m−3


Total PAHs811.201002.74910.5995.9710.54678.43809.95746.7265.918.83291.99430.91340.2478.5823.10

Similar results were obtained in the work of Lin et al. [10] examining the content of PAHs in exhaust gases of various biodiesel mixtures. The data presented in the publication showed that the summary contents of PAHs in diesel exhaust fumes totaled 7.420 ng m−3, while in the mixture of plant biodiesel B50—3,490 ng m−3 meaning a reduction of PAHs at the level of 52%. In the publication, similarly as in the results obtained in this work, the main contents of PAHs is constituted by low-molecular PAHs, including naphthalene, fluorene, phenanthrene, fluoranthene, and pyrene. At the same time, when comparing the results published in the work of Lin et al [10] with the results in Table 4, a significant differences in the contents of benzo(a)anthracene and benzo(a)pyrene reveals. The contents of benzo(a)anthracene in the examined exhaust gases of various fuel mixtures are fairly significant (resp. 340 and 90 ng m−3 for 100% ON and B40) in comparison with other hydrocarbons. However, in the work of Lin et al. [10] the concentration of this compound differs from 6.2 to 3.15 ng m−3 for ON and B50. The total concentration of benzo(a)pyrene determined by the authors comes to 11 to 4.9 ng m3 for ON and B50 respectively, but this compound was not identified in samples taken on ELPI (Table 4).

The differences in concentrations and contents of respective PAHs in diesel engine exhaust fumes were influenced by the type and operation of the engine, including the type of injections, power, capacity, applied filters and diesel and biodiesel fuels, duration of engine operation, and duration of measurements. The differences between the results for individual PAHs presented in this work and in the publication [10] may arise from dissimilarities in the type of engine on which the study was conducted, as well as from the type of fuel, in both cases being a subject to comparison. Moreover, since during the launch of a cold engine a substantial part of particulates is formed in the cold exhaust system, the size, the form, and the composition of a particulate matter highly depends on the location within the cylinder-exhaust system-atmosphere unit where they are intercepted.

4. Conclusion

The main contents in exhaust gases from diesel engine, independently of the type of fuel used in the study, is constituted by the particles fraction of diameters <0.25 μm, which was confirmed by the results of actual measurements with the use of ELPI. The presented studies strongly indicates that adding B100 bioester to commonly used diesel fuel (ON) caused a reduction of a total emission of particles and thus a reduction in the amount of toxic substances adsorbed on them. In B40 exhaust fumes, the average summary contents of PAHs came to a reduction of PAHs in the fumes by 62% when compared to the contents of PAHs in ON fumes. The analysis of chemical composition of dp <0.25 μm exhaust gas fraction showed that 3- and 4-ring aromatic hydrocarbons dominated in exhaust gas of diesel fuel (ON), while in B40 single PAHs with the number of rings of 4 and 5 prevailed. These compounds are more carcinogenic PAHs due to their TEQ values [29].


The paper was prepared based on the results obtained within the National Programme: “Improvement of Safety and Working Conditions” (2011–2013). The Central Institute for Labour Protection-National Research Institute is the coordinator of the programme.


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Copyright © 2013 Małgorzata Szewczyńska et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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