COMPARISON OF SAMPLING METHODS FOR CARBONACEOUS AEROSOLS IN AMBIENT AIR

被引:68
作者
HERING, SV
APPEL, BR
CHENG, W
SALAYMEH, F
CADLE, SH
MULAWA, PA
CAHILL, TA
ELDRED, RA
SUROVIK, M
FITZ, D
HOWES, JE
KNAPP, KT
STOCKBURGER, L
TURPIN, BJ
HUNTZICKER, JJ
ZHANG, XQ
MCMURRY, PH
机构
[1] UNIV CALIF LOS ANGELES,DEPT CHEM ENGN,LOS ANGELES,CA 90024
[2] CALIF DEPT HLTH SERV,AIR & IND HYG LAB,BERKELEY,CA 94704
[3] GM CORP,RES LABS,WARREN,MI 48090
[4] UNIV CALIF DAVIS,CROCKER NUCL LAB,DAVIS,CA 95616
[5] AEROVIRONMENT INC,MONROVIA,CA 91016
[6] ENVIRONM C-E ENVIRONM INC,CAMARILLO,CA 93010
[7] US EPA,MD46,RES TRIANGLE PK,NC 27711
[8] OREGON GRAD CTR,BEAVERTON,OR 97006
[9] UNIV MINNESOTA,DEPT MECH ENGN,MINNEAPOLIS,MN 55455
关键词
D O I
10.1080/02786829008959340
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Measurement methods for fine particle carbon were compared under field sampling conditions. Sampling methods included filtration, impaction, and adsorption-corrected filtration. Systems were operated side-by-side for nine consecutive days in the Los Angeles Basin. Analytical methods were compared separately. For organiccarbon and total carbon, ambient measurements showed greater variability than could be accounted for by differences in analytical methods, and these differences are attributed to sampling methodology. The highest reported concentrations were obtained by quartz filter sampling; the lowest were from the sum of the impactor stages (excluding the quartz afterfilters). Positive artifact from the adsorption of gaseous vapors on quartz fiber filters was significant. However, correction for vapor adsorption by subtraction of the carbon value on the second of two filters in series did not completely eliminate the dependence of the apparent total aerosol carbon concentration on filter face velocity or sample duration. © 1990 Elsevier Science Publishing Co., Inc.
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页码:200 / 213
页数:14
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