Hydrocarbon emission fingerprints from contemporary vehicle/engine technologies with conventional and new fuels

Abstract The present paper presents results from the analysis of 29 individual C2–C9 hydrocarbons (HCs) specified in the European Commission Ozone Directive. The 29 HCs are measured in exhaust from common, contemporary vehicle/engine/fuel technologies for which very little or no data is available in the literature. The obtained HC emission fingerprints are compared with fingerprints deriving from technologies that are being phased out in Europe. Based on the total of 138 emission tests, thirteen type-specific fingerprints are extracted (Mean ± SD percentage contributions from individual HCs to the total mass of the 29 HCs), essential for receptor modelling source apportionment. The different types represent exhaust from Euro3 and Euro4 light-duty (LD) diesel and petrol-vehicles, Euro3 heavy-duty (HD) diesel exhaust, and exhaust from 2-stroke preEuro, Euro1 and Euro2 mopeds. The fuels comprise liquefied petroleum gas, petrol/ethanol blends (0–85% ethanol), and mineral diesel in various blends (0–100%) with fatty acid methyl esters, rapeseed methyl esters palm oil methyl esters, soybean oil methyl or sunflower oil methyl esters. Type-specific tracer compounds (markers) are identified for the various vehicle/engine/fuel technologies. An important finding is an insignificant effect on the HC fingerprints of varying the test driving cycle, indicating that combining HC fingerprints from different emission studies for receptor modelling purposes would be a robust approach. The obtained results are discussed in the context of atmospheric ozone formation and health implications from emissions (mg km−1 for LD and mopeds and mg kW h−1 for HD, all normalised to fuel consumption: mg dm−3 fuel) of the harmful HCs, benzene and 1,3-butadiene. Another important finding is a strong linear correlation of the regulated “total” hydrocarbon emissions (tot-HC) with the ozone formation potential of the 29 HCs (ΣPO3 = (1.66 ± 0.04) × tot-RH; r2 = 0.93). Tot-HC is routinely monitored in emission control laboratories, whereas C2–C9 are not. The revealed strong correlations broadens the usability of data from vehicle emission control laboratories and facilitates the comparison of the ozone formation potential of HCs in exhaust from of old and new vehicle/engine/fuel technologies.

[1]  Hsi-Hsien Yang,et al.  Comparative study of regulated and unregulated air pollutant emissions before and after conversion of automobiles from gasoline power to liquefied petroleum gas/gasoline dual-fuel retrofits. , 2007, Environmental science & technology.

[2]  Martini Giorgio,et al.  Effect of Fuel Ethanol Content on Exhaust Emissions of a Flexible Fuel Vehicle , 2009 .

[3]  Kwangsam Na,et al.  Determination of VOC source signature of vehicle exhaust in a traffic tunnel. , 2006, Journal of environmental management.

[4]  Y. Kim,et al.  Chemical mass balance receptor model applied to ambient C2-C9 VOC concentration in Seoul, Korea : Effect of chemical reaction losses , 2007 .

[5]  Farfaletti Casali Arianna,et al.  Physical & Chemical Characterization of Emissions from 2-Stroke Motorcycles - Comparison with 4-Stroke Engines , 2009 .

[6]  Bernardo Tormos,et al.  Hydrocarbon emissions speciation in diesel and biodiesel exhausts , 2009 .

[7]  Min Shao,et al.  Source profiles of volatile organic compounds (VOCs) measured in China. Part I , 2008 .

[8]  Manfred Baerns,et al.  Basic principles in applied catalysis , 2004 .

[9]  Ankur Kansal,et al.  Sources and reactivity of NMHCs and VOCs in the atmosphere: a review. , 2009, Journal of hazardous materials.

[10]  Isobel J. Simpson,et al.  C1–C8 volatile organic compounds in the atmosphere of Hong Kong: Overview of atmospheric processing and source apportionment , 2007 .

[11]  J. Galloo,et al.  Characterising sources and sinks of rural VOC in eastern France. , 2004, Chemosphere.

[12]  W. Carter Development of Ozone Reactivity Scales for Volatile Organic Compounds , 1994 .

[13]  Judith C. Chow,et al.  Review of volatile organic compound source apportionment by chemical mass balance , 2001 .

[14]  Alois Krasenbrink,et al.  Effect of water/fuel emulsions and a cerium-based combustion improver additive on HD and LD diesel exhaust emissions. , 2005, Environmental science & technology.

[15]  Michael J. Kleeman,et al.  MEASUREMENT OF EMISSIONS FROM AIR POLLUTION SOURCES. 2. C1 THROUGH C30 ORGANIC COMPOUNDS FROM MEDIUM DUTY DIESEL TRUCKS , 1999 .

[16]  R. Atkinson Gas-phase tropospheric chemistry of organic compounds: a review , 1990 .

[17]  Chih-Chung Chang,et al.  Source apportionment of ambient volatile organic compounds in the Pearl River Delta, China. Part II , 2008 .

[18]  Peter Wåhlin,et al.  COPREM—A multivariate receptor model with a physical approach , 2003 .

[19]  Chih-Chung Chang,et al.  Assessment of reducing ozone forming potential for vehicles using liquefied petroleum gas as an alternative fuel , 2001 .

[20]  Sergio Machado Corrêa,et al.  Carbonyl emissions in diesel and biodiesel exhaust. , 2008 .

[21]  Michael J Kleeman,et al.  Measurement of emissions from air pollution sources. 5. C1-C32 organic compounds from gasoline-powered motor vehicles. , 2002, Environmental science & technology.

[22]  Wen-Yinn Lin,et al.  Air pollutant emission factors from new and in-use motorcycles , 2000 .

[23]  T. Doǧu,et al.  Ethylene and diethyl-ether production by dehydration reaction of ethanol over different heteropolyacid catalysts , 2007 .

[24]  O. Sánchez-Ccoyllo,et al.  Measurements of atmospheric carboxylic acids and carbonyl compounds in São Paulo City, Brazil. , 2001, Environmental science & technology.

[25]  R. Friedrich,et al.  Compilation of a database on the composition of anthropogenic VOC emissions for atmospheric modeling in Europe , 2007 .

[26]  C. Astorga,et al.  Semicontinuous GC analysis and receptor modelling for source apportionment of ozone precursor hydrocarbons in Bresso, Milan, 2003. , 2005, Journal of chromatography. A.

[27]  R. Derwent,et al.  Multi-day ozone formation for alkenes and carbonyls investigated with a master chemical mechanism under European conditions , 2005 .

[28]  Chang Yu Yang,et al.  The speciation of volatile organic compounds (VOCs) from motorcycle engine exhaust at different driving modes , 2003 .

[29]  Nadine Locoge,et al.  Using a source-receptor approach to characterise VOC behaviour in a French urban area influenced by industrial emissions. Part I: study area description, data set acquisition and qualitative data analysis of the data set. , 2008, The Science of the total environment.

[30]  Randal S. Martin,et al.  Potential Air Quality Effects of Using Ethanol−Gasoline Fuel Blends: A Field Study in Albuquerque, New Mexico , 1997 .

[31]  S Latham,et al.  A reference book of driving cycles for use in the measurement of road vehicle emissions , 2009 .

[32]  B. Dimitriades Scientific Basis for the VOC Reactivity Issues Raised by Section 183(e) of the Clean Air Act Amendments of 1990. , 1996, Journal of the Air & Waste Management Association.

[33]  J. Galloo,et al.  Developing receptor-oriented methods for non-methane hydrocarbon characterisation in urban air. Part II: source apportionment , 2003 .

[34]  J. Galloo,et al.  Developing receptor-oriented methods for non-methane hydrocarbon characterisation in urban air—Part I: source identification , 2003 .

[35]  Robert Vidon,et al.  Emissions of unregulated pollutants from European gasoline and diesel passenger cars , 2006 .

[36]  Jan Czerwinski,et al.  Research on Particle Emissions of Modern 2-Stroke Scooters , 2006 .

[37]  A. Tudos,et al.  Quantification of airborne fossil and biomass carbonylic carbon by combined radiocarbon and liquid chromatography mass spectrometry , 2001 .

[38]  Dongmin Luo,et al.  Environmental chamber study of maximum incremental reactivities of volatile organic compounds , 1995 .

[39]  Lisa Graham,et al.  Emissions from light duty gasoline vehicles operating on low blend ethanol gasoline and E85 , 2008 .