Continuous wet denuder measurements of atmospheric nitric and nitrous acids during the 1999 Atlanta Supersite

被引:51
作者
Zhang, GF
Slanina, S
Boring, CB
Jongejan, PAC
Dasgupta, PK [1 ]
机构
[1] Texas Tech Univ, Dept Chem & Biochem, Lubbock, TX 79409 USA
[2] Netherlands Energy Res Fdn, NL-1755 ZG Petten, Netherlands
关键词
D O I
10.1016/S1352-2310(02)01011-7
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Two different measurement methods for atmospheric nitric and nitrous acid during the Atlanta Supersite study are described and compared. Both approaches combined wet denuder collection coupled to ion chromatographic analysis. One of these utilized a rotating wet annular denuder maintained indoor with a very dilute Na2CO3 solution as an absorber, operated by the Energieonderzoek Centrum Nederland (ECN), ion chromatography (IC) being conducted with a carbonate eluent system. Data from this instrument was available for a 15 min sample every hour. The other wet denuder was of the parallel plate design and was deployed on the roof of the measurement shelter. This device used dilute H2O2 solution as an absorber and was coupled to an IC operated with a hydroxide eluent. Operated by Texas Tech University (TTU), this instrument provided data with 10 min time resolution. When both instruments were seemingly operating properly, data from TTU and ECN instruments were well correlated, although the peak HNO3 values during high NO2/NOy periods were lower for the TTU instrument. Daily peaks in HNO3, typically ranging in magnitude between 3 and 6 ppbv (7.8 ppbv registered by the ECN instrument on the highest NOy day) were observed. HONO results from both TTU and ECN instruments exhibited strong diurnal variations with nighttime peaks up to similar to 5 ppbv. Data from the middle of the study period for the two instruments were correlated with a r(2) value of 0.78. The relationship was not statistically distinguishable from a 1:1 correspondence. A similar correlation of r(2) = 0.76 was observed for the HNO3 data; in this case the peak concentrations occurring in day time. (C) 2003 Elsevier Science Ltd. All rights reserved.
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页码:1351 / 1364
页数:14
相关论文
共 58 条
[1]  
ALICKE B, 2003, IN PRESS J GEOPHYSIC
[2]   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
[3]   TRENDS, SEASONAL-VARIATIONS, AND ANALYSIS OF HIGH-ELEVATION SURFACE NITRIC-ACID, OZONE, AND HYDROGEN-PEROXIDE [J].
ANEJA, VP ;
CLAIBORN, CS ;
LI, Z ;
MURTHY, A .
ATMOSPHERIC ENVIRONMENT, 1994, 28 (10) :1781-1790
[4]   MEASUREMENT OF ATMOSPHERIC NITRIC-ACID BY THE FILTER METHOD AND COMPARISONS WITH THE TUNABLE DIODE-LASER AND OTHER METHODS [J].
ANLAUF, KG ;
MACTAVISH, DC ;
WIEBE, HA ;
SCHIFF, HI ;
MACKAY, GI .
ATMOSPHERIC ENVIRONMENT, 1988, 22 (08) :1579-1586
[5]   INTERCOMPARISON OF ATMOSPHERIC NITRIC-ACID MEASUREMENTS AT ELEVATED AMBIENT CONCENTRATIONS [J].
ANLAUF, KG ;
WIEBE, HA ;
TUAZON, EC ;
WINER, AM ;
MACKAY, GI ;
SCHIFF, HI ;
ELLESTAD, TG ;
KNAPP, KT .
ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1991, 25 (02) :393-399
[6]   COMPARISON OF ATMOSPHERIC NITROUS-ACID MEASUREMENTS BY ANNULAR DENUDER AND DIFFERENTIAL OPTICAL-ABSORPTION SYSTEMS [J].
APPEL, BR ;
WINER, AM ;
TOKIWA, Y ;
BIERMANN, HW .
ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1990, 24 (03) :611-616
[7]   SIMULTANEOUS NITRIC-ACID, PARTICULATE NITRATE AND ACIDITY MEASUREMENTS IN AMBIENT AIR [J].
APPEL, BR ;
WALL, SM ;
TOKIWA, Y ;
HAIK, M .
ATMOSPHERIC ENVIRONMENT, 1980, 14 (05) :549-554
[8]   SAMPLING OF NITRATES IN AMBIENT AIR [J].
APPEL, BR ;
TOKIWA, Y ;
HAIK, M .
ATMOSPHERIC ENVIRONMENT, 1981, 15 (03) :283-289
[9]  
APPEL BR, 1988, ATMOS ENVIRON, V22, P549
[10]   MEASUREMENTS OF NITROUS-ACID IN AN URBAN AREA [J].
ATKINSON, R ;
CARTER, WPL ;
PITTS, JN ;
WINER, AM .
ATMOSPHERIC ENVIRONMENT, 1986, 20 (02) :408-409