Iodine concentration and availability in atmospheric aerosol

被引:59
作者
Baker, AR [1 ]
Thompson, D
Campos, MLAM
Parry, SJ
Jickells, TD
机构
[1] Univ E Anglia, Sch Environm Sci, Norwich NR4 7TJ, Norfolk, England
[2] Univ London Imperial Coll Sci Technol & Med, Environm Anal Sect, TH Huxley Sch Environm Earth Sci & Engn, Ascot SL5 7TE, Berks, England
关键词
inorganic iodine; organic iodine; neutron activation; voltammetry; aqueous extraction;
D O I
10.1016/S1352-2310(00)00208-9
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Iodine has been determined in aerosol samples collected at a coastal site in southeast England using instrumental neutron activation analysis (INAA) and by an electrochemical technique, after aqueous extraction. Size distribution and enrichment factor data for the samples are consistent with a non-sea-salt source of iodine, presumably gas-to-particle conversion of volatile iodocarbons. On average, only similar to 70% of INAA (i.e. total) iodine could be released from the aerosols as inorganic iodine by aqueous extraction at 95 degrees C. Extraction at a more environmentally realistic temperature (20 degrees C) decreased this yield to similar to 25%. Through the use of high-energy UV light, which is known to destroy organic matter, the yield of aqueous extractable iodine at the lower temperature was increased for some samples. Thus, it appears likely that iodine is present in aerosol in varying proportions as soluble inorganic iodine, soluble organic iodine and insoluble, or unextractable, iodine. The different characteristics of these fractions are likely to have significant impacts on the cycling and reactivity of iodine in the atmosphere. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:4331 / 4336
页数:6
相关论文
共 29 条
[1]   Iodine oxide in the marine boundary layer [J].
Alicke, B ;
Hebestreit, K ;
Stutz, J ;
Platt, U .
NATURE, 1999, 397 (6720) :572-573
[2]   Characterization of the Bermuda tropospheric aerosol by combined individual-particle and bulk-aerosol analysis [J].
Anderson, JR ;
Buseck, PR ;
Patterson, TL ;
Arimoto, R .
ATMOSPHERIC ENVIRONMENT, 1996, 30 (02) :319-338
[3]   Atmospheric aerosols: Biogeochemical sources and role in atmospheric chemistry [J].
Andreae, MO ;
Crutzen, PJ .
SCIENCE, 1997, 276 (5315) :1052-1058
[4]   CHEMICAL-COMPONENTS OF LOWER TROPOSPHERIC AEROSOLS IN THE HIGH ARCTIC - 6 YEARS OF OBSERVATIONS [J].
BARRIE, LA ;
BARRIE, MJ .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 1990, 11 (03) :211-226
[5]   A comparison of methyl iodide emissions from seawater and wet depositional fluxes of iodine over the southern North Sea [J].
Campos, MLAM ;
Nightingale, PD ;
Jickells, TD .
TELLUS SERIES B-CHEMICAL AND PHYSICAL METEOROLOGY, 1996, 48 (01) :106-114
[6]   New approach to evaluating dissolved iodine speciation in natural waters using cathodic stripping voltammetry and a storage study for preserving iodine species [J].
Campos, MLAM .
MARINE CHEMISTRY, 1997, 57 (1-2) :107-117
[7]   IODINE - ITS POSSIBLE ROLE IN TROPOSPHERIC PHOTOCHEMISTRY [J].
CHAMEIDES, WL ;
DAVIS, DD .
JOURNAL OF GEOPHYSICAL RESEARCH-OCEANS, 1980, 85 (NC12) :7383-7398
[8]   ARE THERE INTERACTIONS OF IODINE AND SULFUR SPECIES IN MARINE AIR PHOTOCHEMISTRY [J].
CHATFIELD, RB ;
CRUTZEN, PJ .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1990, 95 (D13) :22319-22341
[9]   ATMOSPHERIC INPUTS OF DISSOLVED ORGANIC NITROGEN TO THE OCEANS [J].
CORNELL, S ;
RENDELL, A ;
JICKELLS, T .
NATURE, 1995, 376 (6537) :243-246
[10]   Water-soluble organic nitrogen in atmospheric aerosol: a comparison of UV and persulfate oxidation methods [J].
Cornell, SE ;
Jickells, TD .
ATMOSPHERIC ENVIRONMENT, 1999, 33 (05) :833-840