Ground-based and airborne measurements of nonmethane hydrocarbons in BERLIOZ:: Analysis and selected results

被引:29
作者
Winkler, J
Blank, P
Glaser, K
Gomes, JAG
Habram, M
Jambert, C
Jaeschke, W
Konrad, S
Kurtenbach, R
Lenschow, P
Lörzer, JC
Perros, PE
Pesch, M
Prümke, HJ
Rappenglück, B
Schmitz, T
Slemr, F
Volz-Thomas, A
Wickert, B
机构
[1] Forschungszentrum Julich, Inst Chem & dynam Geosphare 2, D-52425 Julich, Germany
[2] Senatsverwaltung Stadtentwicklung Umweltschutz &, D-10173 Berlin, Germany
[3] Brandenburg Tech Univ Cottbus, Lehrstuhl Luftchem & Luftreinhaltung, D-03044 Cottbus, Germany
[4] Tech Univ Munich, Dept Okol, Lehrstuhl Bioklimatol & Immiss Forsch, D-85354 Freising Weihenstephan, Germany
[5] Goethe Univ Frankfurt, Zentrum Umweltforsch, D-60325 Frankfurt, Germany
[6] Univ Stuttgart, IER, D-70569 Stuttgart, Germany
[7] Univ Stuttgart, IVD, D-70569 Stuttgart, Germany
[8] Berg Univ Wuppertal, D-42097 Wuppertal, Germany
[9] Fraunhofer Inst Atmosphar Umweltforsch, D-82467 Garmisch Partenkirchen, Germany
[10] Univ Paris 12, LISA, UMR 7583, F-94010 Creteil, France
关键词
nonmethane hydrocarbons; pollution roses; toluene/benzene ratio; city plume; isoprene; NMHC/CO ratios; emission inventory;
D O I
10.1023/A:1015709214016
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
During the Berlin Ozone Experiment BERLIOZ in July-August 1998 quasi-continuous measurements of C-2-C-12 nonmethane hydrocarbons (NMHCs) were carried out at 10 sites in and around the city of Berlin using on-line gas-chromatographic systems (GCs) with a temporal resolution of 20-120 minutes. Additional airborne NMHC measurements were made using canister sampling on three aircraft and an on-line GC system on a fourth aircraft. The ground based data are analyzed to characterize the different sites and to identify the influence of emissions from Berlin on its surroundings. Benzene mixing ratios at the 4 rural sites were rather low (<0.5 ppbv). Berlin (and the surrounding highway ring) was identified as the main source of anthropogenic NMHCs at Eichstadt and Blossin, whilst other sources were important at the furthermost site Menz. The median toluene/benzene concentration ratio in Berlin was 2.3 ppbv/ppbv, agreeing well with measurements in other German cities. As expected, the ratios at the background sites decreased with increasing distance to Berlin and were usually around one or below. On 20 and 21 July, the three northwesterly sites were situated downwind of Berlin and thus were influenced by its emissions. Considering the distance between the sites and the windspeed, the city plume was observed at reasonable time scales, showing decreasing toluene/benzene ratios of 2.3, 1.6 and 1.3 with increasing distance from Berlin. Isoprene was the only biogenic NMHC measured at BERLIOZ. It was the most abundant compound at the background sites on the hotter days, dominating the local NMHC reactivity with averaged contributions to the total OH loss rate of 51% and 70% at Pabstthum and Blossin, respectively. Emission ratios (relative to CO and to the sum of analysed NMHCs) were derived from airborne measurements. The comparison with an emission inventory suggests traffic-related emissions to be the predominating source of the considered hydrocarbon species. Problems were identified with the emission inventory for propane, ethene and pentanes.
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页码:465 / 492
页数:28
相关论文
共 51 条
[1]   Atmospheric chemistry of VOCs and NOx [J].
Atkinson, R .
ATMOSPHERIC ENVIRONMENT, 2000, 34 (12-14) :2063-2101
[2]  
ATKINSON R, 1994, J PHYS CHEM REF DATA, pR1
[3]   Studying the city plume of Berlin on 20 July 1998 with three different modelling approaches [J].
Becker, A ;
Scherer, B ;
Memmesheimer, M ;
Geiss, H .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 2002, 42 (01) :41-70
[4]   ENVIRONMENTAL CHAMBER STUDY OF MAXIMUM INCREMENTAL REACTIVITIES OF VOLATILE ORGANIC-COMPOUNDS [J].
CARTER, WPL ;
PIERCE, JA ;
LUO, DM ;
MALKINA, IL .
ATMOSPHERIC ENVIRONMENT, 1995, 29 (18) :2499-2511
[5]   OZONE PRECURSOR RELATIONSHIPS IN THE AMBIENT ATMOSPHERE [J].
CHAMEIDES, WL ;
FEHSENFELD, F ;
RODGERS, MO ;
CARDELINO, C ;
MARTINEZ, J ;
PARRISH, D ;
LONNEMAN, W ;
LAWSON, DR ;
RASMUSSEN, RA ;
ZIMMERMAN, P ;
GREENBERG, J ;
MIDDLETON, P ;
WANG, T .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1992, 97 (D5) :6037-6055
[6]   Ozone and PAN formation inside and outside of the Berlin plume -: Process analysis and numerical process simulation [J].
Corsmeier, U ;
Kalthoff, N ;
Vogel, B ;
Hammer, MU ;
Fiedler, F ;
Kottmeier, C ;
Volz-Thomas, A ;
Konrad, S ;
Glaser, K ;
Neininger, B ;
Lehning, M ;
Jaeschke, W ;
Memmesheimer, M ;
Rappenglück, B ;
Jakobi, G .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 2002, 42 (01) :289-321
[7]   Photochemical ozone creation potentials for organic compounds in northwest Europe calculated with a master chemical mechanism [J].
Derwent, RG ;
Jenkin, ME ;
Saunders, SM ;
Pilling, MJ .
ATMOSPHERIC ENVIRONMENT, 1998, 32 (14-15) :2429-2441
[8]   ANALYSIS AND INTERPRETATION OF AIR-QUALITY DATA FROM AN URBAN ROADSIDE LOCATION IN CENTRAL LONDON OVER THE PERIOD FROM JULY 1991 TO JULY 1992 [J].
DERWENT, RG ;
MIDDLETON, DR ;
FIELD, RA ;
GOLDSTONE, ME ;
LESTER, JN ;
PERRY, R .
ATMOSPHERIC ENVIRONMENT, 1995, 29 (08) :923-946
[9]   Analysis and interpretation of the continuous hourly monitoring data for 26 C2-C8 hydrocarbons at 12 United Kingdom sites during 1996 [J].
Derwent, RG ;
Davies, TJ ;
Delaney, M ;
Dollard, GJ ;
Field, RA ;
Dumitrean, P ;
Nason, PD ;
Jones, BMR ;
Pepler, SA .
ATMOSPHERIC ENVIRONMENT, 2000, 34 (02) :297-312
[10]   Influence of continental sources on oceanic air composition at the eastern edge of the North Atlantic Ocean, TOR 1992-1995 [J].
Fenneteaux, I ;
Colin, P ;
Etienne, A ;
Boudries, H ;
Dutot, AL ;
Perros, PE ;
Toupance, G .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 1999, 32 (02) :233-280