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CONDENSATION SAMPLING OF SOLUBLE TRACE GASES IN THE ATMOSPHERE.

机译:大气中可溶痕量气体的冷凝采样。

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摘要

The potential of a condensate method for sampling atmospheric trace gases is investigated. A theoretical approach to the collection of condensate by a cooled surface is presented, followed by an experimental procedure and verification of the method. Heat and mass transfer problems are solved to give distributions of temperature, velocity and mass concentration. From these distributions, collection rates for water vapor, trace gases, and particulates are derived. It is shown that the collection of particulates is negligible in most cases when compared to the collection of gases in the condensate; highly soluble gases are sampled with the greatest efficiency. Experimentally, a plate, cooled to below the ambient dew point temperature, collected condensate which was subsequently analyzed for various components. Atmospheric concentrations were determined from the corresponding species in the condensate. Several trace gases have been detected by the condensate method. Concentrations of two of these, ammonia and nitric acid, are compared with filter methods, with reasonably good agreement. Comparison is also made with concentrations of ammonia, formaldehyde, nitric acid and nitrous acid found by others under similar conditions. Typical daily variations of trace components in more remote areas surrounding Tucson, Arizona, are presented in an attempt to estimate background Southwest U.S.A. levels; these are as follows: 1.0 ppb for ammonia, 0.5 ppb for formaldehyde, 0.1 ppb for nitrous acid, 0.4 ppb for nitric acid, 1.1 ppb for formic acid, 0.9 ppb for acetic acid, 0.3 ppb for sulfur dioxide, 0.3 ppb for hydrochloric acid and 1 ppb for hydrogen peroxide. The diurnal variation of these gases and relationship between them is discussed. Possible sources of error in the condensate method of sampling are considered. The collection rate of water vapor is measured and compared to that theoretically predicted; explanations are presented for the discrepancy between the two. The sensitivity to errors in the measurement of the collection temperature and dew point temperature is determined.
机译:研究了使用冷凝液采样大气痕量气体的潜力。提出了一种通过冷却表面收集冷凝水的理论方法,然后进行了实验程序并对该方法进行了验证。解决了传热和传质问题,以给出温度,速度和质量浓度的分布。从这些分布中,可以得出水蒸气,微量气体和微粒的收集率。结果表明,与冷凝液中气体的收集相比,大多数情况下颗粒物的收集可以忽略不计。高溶解度的气体以最大的效率采样。实验上,将一块冷却至环境露点温度以下的板收集冷凝液,然后对冷凝液进行各种成分分析。由冷凝物中的相应物质确定大气浓度。通过冷凝法检测到了几种痕量气体。将氨气和硝酸中的两种浓度与过滤器方法进行比较,结果吻合得很好。还比较了其他人在类似条件下发现的氨,甲醛,硝酸和亚硝酸的浓度。为了估算美国西南部背景水平,提出了亚利桑那州图森市附近较偏远地区痕量成分的典型每日变化;如下:氨水1.0 ppb,甲醛0.5 ppb,亚硝酸0.1 ppb,硝酸0.4 ppb,甲酸1.1 ppb,乙酸0.9 ppb,二氧化硫0.3 ppb,盐酸0.3 ppb过氧化氢为1 ppb。讨论了这些气体的日变化及其之间的关系。考虑凝结水采样方法中可能的误差来源。测量水蒸气的收集速率,并将其与理论上预测的相比较;解释了两者之间的差异。确定对收集温度和露点温度的测量中的误差的敏感性。

著录项

  • 作者

    FARMER JOSEPH CARL.;

  • 作者单位
  • 年度 1982
  • 总页数
  • 原文格式 PDF
  • 正文语种 en
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