کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6340836 | 1620383 | 2014 | 7 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Chemical composition of the inorganic fraction of cloud-water at a high altitude station in West India
ترجمه فارسی عنوان
ترکیب شیمیایی از کسر معدنی آب ابر در ایستگاه ارتفاع بالا در غرب هند
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موضوعات مرتبط
مهندسی و علوم پایه
علوم زمین و سیارات
علم هواشناسی
چکیده انگلیسی
Data from a ground-based cloud-water collection system intercepting water from clouds at a mountain field station, Sinhagad near Pune in India are presented. This study was part of an Indo-Swedish Collaboration Project on Atmospheric Brown Cloud-Asia (ABC-A). Cloud-water and rainwater (wet-only) samples were collected during June 2007-Dec. 2010. Concentrations of major anions and cations were determined. Ion concentrations were generally higher (NO3â, about 8 times; SO42â and K+, 5 times; NH4+, 4 times and Clâ, Na+, Ca2+, Mg2+ 3 times) in cloud-water samples than in rainwater samples collected during the same days. The average pH of cloud-water samples was 6.0 with about 20% of the values below 5.6 and only 4% less than 5.0. Despite high concentrations of SO42â and NO3â the cloud water samples were on average not more acidic than rainwater samples. This is different from most of the other studies of cloud-water composition which have noted a substantially higher acidity (i.e. lower pH) in cloud-water than in rainwater. The slightly alkaline (pHÂ >Â 5.6) nature of the cloud-water samples is mainly due to the presence of soil derived calcium carbonate in quantities more than enough to neutralize the acids or their precursors. A separation of the cloud-water data into trajectory groups showed that samples in air-masses having spent the last few days over the Indian sub-continent were in general more acidic (due to anthropogenic emissions) than those collected during days with air-masses of marine origin. A high correlation mutually between Ca2+, Na+, NO3â and SO42â makes it difficult to estimate the contribution to SO42â from different sources. Anthropogenic SO2-emissions and soil dust may both give important contributions.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Atmospheric Environment - Volume 88, May 2014, Pages 59-65
Journal: Atmospheric Environment - Volume 88, May 2014, Pages 59-65
نویسندگان
K.B. Budhavant, P.S.P. Rao, P.D. Safai, L. Granat, H. Rodhe,