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    Electrification Experiments with Agl in the System: Water Vapor, Liquid Water and Ice

    Source: Journal of the Atmospheric Sciences:;1969:;Volume( 026 ):;issue: 004::page 675
    Author:
    Owe Berg, T. G.
    ,
    Gaukler, Thomas A.
    DOI: 10.1175/1520-0469(1969)26<675:EEWAIT>2.0.CO;2
    Publisher: American Meteorological Society
    Abstract: The charge on an AgI particle, freely suspended in an air current of terminal velocity, has been measured at various temperatures, humidities and cooling rates. The wall of the flow pipe serves as a source or sinkfor water vapor, simulating neighbor droplets and ice particles in a cloud. The data show that the AgI particle sorbs water below the dew point and thereby acquires negative charge, that the sorbed water freezes at 0C, and that the electrification is reverisble. There are sudden changes in charge at the onset of sorption at the dew point and at freezing and melting, but the largest changes take place in prolonged and extensive sorption or desorption. The electrification follows an exponential rate law, indicating an autocatalytic process. Ice formation at 0C was also obtained with a dense cloud of AgI and correspondingly small condensate droplets in the expansion chamber. It is concluded that nucleation occurs at 0C, and that super-saturation pertains to the growth of the ice to detacable size. The data are compared with data in the literature. It is concluded that contradictions among published data are the results of differences in experimentalconditions, especially substrate effects in experiments with supported drops. The mechanisms of nucleation,growth and electrification are discussed.
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      Electrification Experiments with Agl in the System: Water Vapor, Liquid Water and Ice

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    https://yetl.yabesh.ir/yetl1/handle/yetl/4151441
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    contributor authorOwe Berg, T. G.
    contributor authorGaukler, Thomas A.
    date accessioned2017-06-09T14:15:14Z
    date available2017-06-09T14:15:14Z
    date copyright1969/07/01
    date issued1969
    identifier issn0022-4928
    identifier otherams-15736.pdf
    identifier urihttp://onlinelibrary.yabesh.ir/handle/yetl/4151441
    description abstractThe charge on an AgI particle, freely suspended in an air current of terminal velocity, has been measured at various temperatures, humidities and cooling rates. The wall of the flow pipe serves as a source or sinkfor water vapor, simulating neighbor droplets and ice particles in a cloud. The data show that the AgI particle sorbs water below the dew point and thereby acquires negative charge, that the sorbed water freezes at 0C, and that the electrification is reverisble. There are sudden changes in charge at the onset of sorption at the dew point and at freezing and melting, but the largest changes take place in prolonged and extensive sorption or desorption. The electrification follows an exponential rate law, indicating an autocatalytic process. Ice formation at 0C was also obtained with a dense cloud of AgI and correspondingly small condensate droplets in the expansion chamber. It is concluded that nucleation occurs at 0C, and that super-saturation pertains to the growth of the ice to detacable size. The data are compared with data in the literature. It is concluded that contradictions among published data are the results of differences in experimentalconditions, especially substrate effects in experiments with supported drops. The mechanisms of nucleation,growth and electrification are discussed.
    publisherAmerican Meteorological Society
    titleElectrification Experiments with Agl in the System: Water Vapor, Liquid Water and Ice
    typeJournal Paper
    journal volume26
    journal issue4
    journal titleJournal of the Atmospheric Sciences
    identifier doi10.1175/1520-0469(1969)26<675:EEWAIT>2.0.CO;2
    journal fristpage675
    journal lastpage688
    treeJournal of the Atmospheric Sciences:;1969:;Volume( 026 ):;issue: 004
    contenttypeFulltext
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    DSpace software copyright © 2002-2015  DuraSpace
    نرم افزار کتابخانه دیجیتال "دی اسپیس" فارسی شده توسط یابش برای کتابخانه های ایرانی | تماس با یابش
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