Adsorption of NO2 on carbon aerosol particles in the low ppb range

被引:33
作者
Kalberer, M
Ammann, M
Gäggeler, HW
Baltensperger, U [1 ]
机构
[1] Paul Scherrer Inst, CH-5232 Villigen, Switzerland
[2] Univ Bern, Dept Chem & Biochem, CH-3012 Bern, Switzerland
关键词
heterogeneous chemistry; carbonaceous aerosol; NO2; adsorption;
D O I
10.1016/S1352-2310(98)00390-2
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The interaction of NO2 on carbonaceous aerosol particles in an NO2 concentration range relevant for the troposphere was studied. The adsorption as a function of NO2 concentration (2.5-65 ppb) was investigated along with the dependence on time (1-600 s) and particle concentration. The results exhibit a zero-order process in NO2 for the chemisorption over the measured time and concentration range. The results suggest that the chemisorption reaction is limited by a rapidly established steady-state coverage of a precursor in the form of reversibly adsorbed NO2 which seems to be constant over the whole investigated NO2 concentration range. Within the first 20 s, a chemisorption rate of 2.5 x 10(11) molecules cm(-2) s(-1) was calculated. To estimate a saturation value for the NO2 adsorption on carbonaceous aerosol particles, bulk experiments were performed where the aerosol was deposited on a filter before exposure to NO2. This gives a lower limit for the total NO2 adsorption of about 1 x 10(14) molecules cm(-2) of particle surface area. The measurements show that the concept of the often used sticking coefficient gamma (i.e. the number of adsorbed molecules per number of the total gas-surface collisions) is not a useful parameter to describe the chemisorption of NO2 at low ppb concentration on such complex surfaces as carbonaceous aerosol particles. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2815 / 2822
页数:8
相关论文
共 25 条
[1]   THE STRUCTURE OF HEXANE SOOT-I - SPECTROSCOPIC STUDIES [J].
AKHTER, MS ;
CHUGHTAI, AR ;
SMITH, DM .
APPLIED SPECTROSCOPY, 1985, 39 (01) :143-153
[2]   THE STRUCTURE OF HEXANE SOOT-II - EXTRACTION STUDIES [J].
AKHTER, MS ;
CHUGHTAI, AR ;
SMITH, DM .
APPLIED SPECTROSCOPY, 1985, 39 (01) :154-167
[3]   Heterogeneous production of nitrous acid on soot in polluted air masses [J].
Ammann, M ;
Kalberer, M ;
Jost, DT ;
Tobler, L ;
Rössler, E ;
Piguet, D ;
Gäggeler, HW ;
Baltensperger, U .
NATURE, 1998, 395 (6698) :157-160
[4]   STUDY OF HI, HBR AND NO2 ADSORPTION ON GRAPHITE AND SILVER AEROSOL-PARTICLES USING SHORT-LIVED ISOTOPES [J].
AMMANN, M ;
BALTENSPERGER, U ;
BOCHERT, UK ;
EICHLER, B ;
GAGGELER, HW ;
JOST, DT ;
TURLER, A ;
WEBER, AP .
JOURNAL OF AEROSOL SCIENCE, 1995, 26 (01) :61-70
[5]  
AMMANN M, 1997, OXIDIZING CAPACITY T, P683
[6]  
ATKINS PW, 1994, PHYSICAL CHEM, P996
[7]   SEQUENTIAL, SELECTIVE HOLLOW TUBE PRECONCENTRATION AND CHEMILUMINESCENCE ANALYSIS SYSTEM FOR NITROGEN-OXIDE COMPOUNDS IN AIR [J].
BRAMAN, RS ;
DELACANTERA, MA ;
HAN, QX .
ANALYTICAL CHEMISTRY, 1986, 58 (07) :1537-1541
[8]   Characterization of particles in combustion engine exhaust [J].
Burtscher, H ;
Kunzel, S ;
Huglin, C .
JOURNAL OF AEROSOL SCIENCE, 1998, 29 (04) :389-396
[9]   KINETICS OF THE HEXANE SOOT REACTION WITH NO2/N2O4 AT LOW CONCENTRATION [J].
CHUGHTAI, AR ;
GORDON, SA ;
SMITH, DM .
CARBON, 1994, 32 (03) :405-416
[10]   A SPECTROSCOPIC STUDY OF GASEOUS PRODUCTS OF SOOT-OXIDES OF NITROGEN WATER REACTIONS [J].
CHUGHTAI, AR ;
WELCH, WF ;
AKHTER, MS ;
SMITH, DM .
APPLIED SPECTROSCOPY, 1990, 44 (02) :294-298