TROPOSPHERIC BUDGET OF REACTIVE CHLORINE

被引:254
作者
GRAEDEL, TE [1 ]
KEENE, WC [1 ]
机构
[1] UNIV VIRGINIA,DEPT ENVIRONM SCI,CHARLOTTESVILLE,VA 22903
关键词
D O I
10.1029/94GB03103
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Reactive chlorine in the lower atmosphere (as distinguished from chlorofluorocarbon-derived chlorine in the stratosphere) is important to considerations of precipitation acidity, corrosion, foliar damage, and chemistry of the marine boundary layer. Many of the chlorine-containing gases are difficult to measure, and natural sources appear to dominate anthropogenic sources for some chemical species. As a consequence, no satisfactory budget for reactive chlorine in the lower atmosphere is available. We have reviewed information on sources; source strengths; measurements in gas, aqueous, and aerosol phases; and chemical processes and from those data derive global budgets for nine reactive chlorine species and for reactive chlorine as a whole. The typical background abundance of reactive chlorine in the lower tropospheric is about 1.5 ppbv. The nine species, CH3Cl, CH3 CCl3, HCl, CHClF2, Cl-2* (thought to be HOCl and/or Cl-2), CCl2 = CCl2, CH2Cl2, COCl2, and CHCl3, each contribute at least a few percent to that total. The tropospheric reactive chlorine burden of approximately 8.3 Tg Cl is dominated by CH3Cl (approximate to 45 %) and CH3CCl3 (approximate to 25 %) and appears to be increasing by several percent per year. By far the most vigorous chlorine cycling appears to occur among seasalt aerosol, HCl, and Cl-2*. The principal sources of reactive chlorine are volatilization from seasalt (enhanced by anthropogenically generated reactants), marine algae, volcanoes, and coal combustion (natural sources being thus quite important to the budget). It is anticipated that the concentrations of tropospheric reactive chlorine will continue to increase in the next several decades, particularly near urban areas in the rapidly developing countries.
引用
收藏
页码:47 / 77
页数:31
相关论文
共 248 条
  • [51] FRASER PJ, 1990, BASELINE 88, P49
  • [52] CHEMICAL ELEMENT BALANCES AND IDENTIFICATION OF AIR-POLLUTION SOURCES
    FRIEDLANDER, SK
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1973, 7 (03) : 235 - 240
  • [53] FRIEND JP, 1989, AFEAS20 GLOB OZ RES
  • [54] FRITSCHEN L, 1970, PNW97 USDA FOR SERV
  • [55] ION-CHROMATOGRAPHIC DETERMINATION OF CHLOROACETATE AND DICHLOROACETATE IN PRECIPITATIONS
    FUCHS, GR
    BACHMANN, K
    [J]. FRESENIUS ZEITSCHRIFT FUR ANALYTISCHE CHEMIE, 1987, 327 (02): : 205 - 212
  • [56] THE COMPOSITION OF PRECIPITATION ON AMSTERDAM-ISLAND, INDIAN-OCEAN
    GALLOWAY, JN
    GAUDRY, A
    [J]. ATMOSPHERIC ENVIRONMENT, 1984, 18 (12) : 2649 - 2656
  • [57] THE COMPOSITION OF PRECIPITATION IN REMOTE AREAS OF THE WORLD
    GALLOWAY, JN
    LIKENS, GE
    KEENE, WC
    MILLER, JM
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-OCEANS, 1982, 87 (NC11) : 8771 - 8786
  • [58] THE TEMPORAL AND SPATIAL VARIABILITY OF SCAVENGING RATIOS FOR NSS SULFATE, NITRATE, METHANESULFONATE AND SODIUM IN THE ATMOSPHERE OVER THE NORTH-ATLANTIC OCEAN
    GALLOWAY, JN
    SAVOIE, DL
    KEENE, WC
    PROSPERO, JM
    [J]. ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1993, 27 (02): : 235 - 250
  • [59] ABSORPTION CROSS-SECTIONS FOR GASEOUS CLNO2 AND CL2 AT 298-K - POTENTIAL ORGANIC OXIDANT SOURCE IN THE MARINE TROPOSPHERE
    GANSKE, JA
    BERKO, HN
    FINLAYSONPITTS, BJ
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1992, 97 (D7) : 7651 - 7656
  • [60] GENFA Z, 1989, ENVIRON SCI TECHNOL, V23, P1467, DOI 10.1021/es00070a003