OBSERVATION OF THE DIURNAL-VARIATION OF GASEOUS H2O2 IN LOS-ANGELES AIR USING A CRYOGENIC COLLECTION METHOD

被引:20
作者
SAKUGAWA, H
KAPLAN, IR
机构
[1] Institute of Geophysics and Planetary Physics, University of California, Los Angeles, CA
关键词
D O I
10.1080/02786829008959327
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
During the Carbonaceous Species Method Comparison Study at Glendora, CA in August 11–21, 1986, gaseous H2O2in the air was collected by a cold trap method using dry ice-acetone as a cooling reagent. Sampling time of the H2O2was every 4 hours during the day and 8 hours from 11 p.m. through 7 a.m. (PST). Gaseous H2O2was also collected simultaneously at Duarte and Westwood during the comparison study. After H2O2entrapment from air, H2O2concentration in the defrosted sample was measured by a fluorescence technique. The observed range of gaseous H2O2was 0.08–1.02 (n = 23), 0.10–0.86 (n = 23), and 0.09–0.34 ppb (n= 10) at Glendora, Duarte, and Westwood, respectively. The highest values in H2O2content was found during midday when O3content was maximum and NOxcontent was minimum at all the sites studied. On the other hand, lowest values in H2O2content were observed in the evening through early morning. H2O2concentration was always higher at Glendora than at Duarte and Westwood during midday. This regional variation of gaseous H2O2closely correlated with O3distribution in the Los Angeles Basin. Meteorological data suggest that the transport of atmospheric pollutants in the Basin by sea breeze during daytime from coastal and central to inland areas when the inversion height is low, may be an important process for the generation of H2O2, as well as O3. The H2O2concentration measured by the UCLA method at Glendora is sometimes significantly lower than concentrations measured by aqueous stripping methods, but is similar to values measured by a spectroscopic method. © 1990 Elsevier Science Publishing Co., Inc.
引用
收藏
页码:77 / 85
页数:9
相关论文
共 14 条
[1]  
CALVERT JG, 1983, ENVIRON SCI TECHNOL, V17, pA428, DOI 10.1021/es00115a727
[2]  
FINLAYSONPITTS BJ, 1986, ATMOSPHERIC CHEM, P1098
[3]   AQUEOUS H2O2 PRODUCTION FROM O-3 IN GLASS IMPINGERS [J].
HEIKES, BG .
ATMOSPHERIC ENVIRONMENT, 1984, 18 (07) :1433-1445
[4]   EVIDENCE FOR AQUEOUS PHASE HYDROGEN-PEROXIDE SYNTHESIS IN THE TROPOSPHERE [J].
HEIKES, BG ;
LAZRUS, AL ;
KOK, GL ;
KUNEN, SM ;
GANDRUD, BW ;
GITLIN, SN ;
SPERRY, PD .
JOURNAL OF GEOPHYSICAL RESEARCH-OCEANS, 1982, 87 (NC4) :3045-3051
[5]   PHOTOCHEMICAL FORMATION OF PEROXIDES IN THE BOUNDARY-LAYER [J].
KLEINMAN, LI .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1986, 91 (D10) :889-904
[6]   AUTOMATED FLUOROMETRIC METHOD FOR HYDROGEN-PEROXIDE IN ATMOSPHERIC PRECIPITATION [J].
LAZRUS, AL ;
KOK, GL ;
GITLIN, SN ;
LIND, JA ;
MCLAREN, SE .
ANALYTICAL CHEMISTRY, 1985, 57 (04) :917-922
[7]   H2O2 AND O-3 IN THE ATMOSPHERE OF LOS-ANGELES AND ITS VICINITY - FACTORS CONTROLLING THEIR FORMATION AND THEIR ROLE AS OXIDANTS OF SO2 [J].
SAKUGAWA, H ;
KAPLAN, IR .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1989, 94 (D10) :12957-12973
[8]   ATMOSPHERIC H2O2 MEASUREMENT - COMPARISON OF COLD TRAP METHOD WITH IMPINGER BUBBLING METHOD [J].
SAKUGAWA, H ;
KAPLAN, IR .
ATMOSPHERIC ENVIRONMENT, 1987, 21 (08) :1791-1798
[9]  
SAKUGAWA H, 1988, DEC AM GEOPH UN FALL
[10]   A HOMOGENEOUS GAS-PHASE MECHANISM FOR USE IN A REGIONAL ACID DEPOSITION MODEL [J].
STOCKWELL, WR .
ATMOSPHERIC ENVIRONMENT, 1986, 20 (08) :1615-1632