ATMOSPHERIC LIGHT-ABSORPTION - A REVIEW

被引:468
作者
HORVATH, H
机构
[1] Institute of Experimental Physics, University of Vienna, Vienna
来源
ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS | 1993年 / 27卷 / 03期
关键词
LIGHT ABSORPTION; LIGHT SCATTERING; AEROSOL; TRACE GASES; SOOT; BLACK CARBON; NO2; COLORATION; DISCOLORATION; VISIBILITY; ALBEDO; CLIMATE CHANGE;
D O I
10.1016/0960-1686(93)90104-7
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The atmosphere interacts both with incoming as well as outgoing light. Two main processes take place: light scattering and light absorption. Whereas light scattering redistributes any light energy in the atmosphere, light absorption converts the light energy to internal energy of the absorbing molecules and eventually transfers it to the surrounding gas as heat. Atmospheric gases absorb light in distinct spectral regions usually at more of less broad bands. Best known is the broad absorption of ozone in the far u.v., being essential for the existence of the biological macromolecules on Earth. Gases known as greenhouse gases, e.g. CO2, CH4, N2O and water vapor absorb a wide range of infrared radiation, and thus are responsible for the greenhouse effects. Since the lifetime of these gases (except water vapor) is considerable, their distribution around the globe is fairly homogeneous. The atmospheric aerosol gives the major contribution to the atmospheric light absorption in the visible and near u.v. and near i.r. Graphitic (black) carbon, the main constituent of soot, is almost exclusively responsible for the light absorption of the particles. The light absorption by aerosols is continuous and covers the whole visible spectral range. It only depends slightly on wavelength. The optical properties of elemental carbon are determined by the size of the particles and their complex refractive index. A variety of refractive indices can be found in the literature for elemental carbon, most likely caused by different production and thus composition of the particles. Soot particles are very efficient in attenuating light; for the average size the particles have more than twice the mass extinction coefficient compared to transparent particles such as ammonium sulfate. The light absorption coefficient of a mixture of elemental carbon and transparent materials is higher for internal than for external mixtures. When incorporated into transparent particles, the absorption properties of elemental carbon can be multiplied and the single scattering albedo will decrease in comparison to an external mixture of the same materials. There are different methods to measure the light absorption coefficient of suspended particles. They can be separated in three groups, depending on the effect or methodology they use, but no standard procedure has been adopted so far. Soot is produced by all combustion processes. Since most fires on Earth are due to humans, then indirectly humans are the major source of light-absorbing aerosol particles. On a global scale black carbon amounts to 1.1-2.5% of the anthropogenic particles and to 0.2-1% of the total emitted particles. The emission factors for elemental carbon are highest for small sources such as diesel motors or fireplaces. The light-absorbing aerosol consists of fine particles, with most particles having diameters less than a few tenths of a micrometer. Particles in the size range of soot particles have an average lifetime of 7 days in the atmosphere, therefore they can be transported over large distances and are also found in remote regions. Since light-absorbing particles have a variety of sources and sinks and they are involved in precipitation cycles, their distribution on the globe is inhomogeneous. Light-absorption coefficients of the atmospheric aerosol reported in the literature differ by more than four orders of magnitudes at different locations, but nevertheless black carbon particles have been found even at very remote areas, such as the South Pole. Although light-absorbing particles are a minority component in the atmospheric aerosol, their effects cannot be neglected: since the mass extinction coefficient of soot is higher by a factor of two to three compared to transparent particles, light-absorbing substances in the atmosphere can cause at some locations up to half of the visibility reduction; light-absorbing substances in the atmosphere can be responsible for the brown appearance of urban hazes and the discoloration of the sky. The light absorption of the atmosphere in the visible (which mainly is due to particulate matter) has to be taken into account when considering radiative properties and climatic consequences. A small temperature increase due to absorption in the visible is to be expected. The value is around a few tenths of a Kelvin, but no general statement on its magnitude is possible, since a large spatial and temporal variation exists and other factors like surface albedo, the optical depth of the aerosol, its incorporation in clouds and humidity growth of the aerosol have to be considered.
引用
收藏
页码:293 / 317
页数:25
相关论文
共 50 条
  • [21] Brown carbon in atmospheric fine particles in Yangzhou, China: Light absorption properties and source apportionment
    Chen, Yanfang
    Xie, Xinchun
    Shi, Zhan
    Li, Yilin
    Gai, Xinyu
    Wang, Junfeng
    Li, Haiwei
    Wu, Yun
    Zhao, Xiuyong
    Chen, Mindong
    Ge, Xinlei
    ATMOSPHERIC RESEARCH, 2020, 244
  • [22] Characterizing winter-time brown carbon: Insights into chemical and light-absorption properties in residential and traffic environments
    Barreira, Luis M.F.
    Aurela, Minna
    Saarikoski, Sanna
    Li, Delun
    Teinilä, Kimmo
    Virkkula, Aki
    Niemi, Jarkko V.
    Manninen, H.E.
    Pirjola, Liisa
    Petäjä, Tuukka
    Rönkkö, Topi
    Timonen, Hilkka
    Science of the Total Environment, 2024, 955
  • [23] Sources and light absorption characteristics of water-soluble organic carbon (WSOC) of atmospheric particles at a remote area in inner Himalayas and Tibetan Plateau
    Li, Yawei
    Yan, Fangping
    Kang, Shichang
    Zhang, Chao
    Chen, Pengfei
    Hu, Zhaofu
    Li, Chaoliu
    ATMOSPHERIC RESEARCH, 2021, 253
  • [24] RETRACTED: Light-absorption enhancement design o ultrathin perovskite solar cells with conformal structure (Retracted Article)
    Tan, Xinyu
    Sun, Lei
    Deng, Can
    Tu, Yiteng
    Shen, Guangming
    Tan, Fengxue
    Guan, Li
    Yan, Wensheng
    JOURNAL OF PHYSICS D-APPLIED PHYSICS, 2018, 51 (24)
  • [25] A filter-based light-absorption measurement with polar photometer: Effects of sampling artefacts from organic carbon
    Vecchi, R.
    Bernardoni, V.
    Paganelli, C.
    Valli, G.
    JOURNAL OF AEROSOL SCIENCE, 2014, 70 : 15 - 25
  • [26] Combined influences of sources and atmospheric bleaching on light absorption of water-soluble brown carbon aerosols
    Fang, Wenzheng
    Andersson, August
    Lee, Meehye
    Zheng, Mei
    Du, Ke
    Kim, Sang-Woo
    Holmstrand, Henry
    Gustafsson, Orjan
    NPJ CLIMATE AND ATMOSPHERIC SCIENCE, 2023, 6 (01)
  • [27] Aerosol light absorption and its measurement: A review
    Moosmueller, H.
    Chakrabarty, R. K.
    Arnott, W. P.
    JOURNAL OF QUANTITATIVE SPECTROSCOPY & RADIATIVE TRANSFER, 2009, 110 (11) : 844 - 878
  • [28] Connecting the Light Absorption of Atmospheric Organic Aerosols with Oxidation State and Polarity
    Jiang, Xiaotong
    Liu, Dantong
    Li, Qian
    Tian, Ping
    Wu, Yangzhou
    Li, Siyuan
    Hu, Kang
    Ding, Shuo
    Bi, Kai
    Li, Ruijie
    Huang, Mengyu
    Ding, Deping
    Chen, Qingcai
    Kong, Shaofei
    Li, Weijun
    Pang, Yu
    He, Ding
    ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2022, 56 (18) : 12873 - 12885
  • [29] Aging of biomass burning emissions in the Indo-Gangetic Plain outflow: Implications for black carbon light-absorption enhancement
    Kompalli, Sobhan Kumar
    Babu, S. Suresh
    Ajith, T. C.
    Moorthy, K. Krishna
    Satheesh, S. K.
    Boopathy, R.
    Das, Trupti
    Liu, Dantong
    Allan, James
    Coe, Hugh
    ATMOSPHERIC RESEARCH, 2023, 294
  • [30] Enhanced light absorption due to the mixing state of black carbon in fresh biomass burning emissions
    Wang, Qiyuan
    Cao, Junji
    Han, Yongming
    Tian, Jie
    Zhang, Yue
    Pongpiachan, Siwatt
    Zhang, Yonggang
    Li, Li
    Niu, Xinyi
    Shen, Zhenxing
    Zhao, Zhuzi
    Tipmanee, Danai
    Bunsomboonsakul, Suratta
    Chen, Yang
    Sun, Jian
    ATMOSPHERIC ENVIRONMENT, 2018, 180 : 184 - 191