Measurement of partial vapor pressure of ammonia over acid ammonium sulfate solutions by an integral method
Petros Koutrakis, Benedict Aurian‐Blajeni
Abstract
Petros Koutrakis, Benedict Aurian‐Blajeni
Abstract
We present a simple, integral, passive method for measuring partial vapor pressure. Integral methods are useful tools when dealing with very low concentrations because collection over extended periods increases the analytical sensitivity. Passive methods have the advantage of not introducing constraints external to the system. The principle of the method used here is to selectively react the substance in the atmosphere over a solution with an immobilized coating on an appropriate support. The reaction product is not volatile, but is soluble and can be extracted in an appropriate solvent and analyzed. The method has been applied to measuring the vapor pressure of ammonia over aqueous solutions. The vapor pressure over ammonium sulfate solutions depends on the acidity of the solutions as well as on the salt concentration. The dependence can be explained with a simple model. Furthermore, using the same model, we calculated the ammonia vapor pressure above different ammonium sulfate/sulfuric acid aqueous solutions as a function of sulfate molarity and percentage of sulfuric acid. The results from the calculations suggest that for ambient ammonia concentrations less than 10 ppb, acid sulfate aerosols are not completely neutralized.
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We present a simple, integral, passive method for measuring partial vapor pressure. Integral methods are useful tools when dealing with very low concentrations because collection over extended periods increases the analytical sensitivity. Passive methods have the advantage of not introducing constraints external to the system. The principle of the method used here is to selectively react the substance in the atmosphere over a solution with an immobilized coating on an appropriate support. The reaction product is not volatile, but is soluble and can be extracted in an appropriate solvent and analyzed. The method has been applied to measuring the vapor pressure of ammonia over aqueous solutions. The vapor pressure over ammonium sulfate solutions depends on the acidity of the solutions as well as on the salt concentration. The dependence can be explained with a simple model. Furthermore, using the same model, we calculated the ammonia vapor pressure above different ammonium sulfate/sulfuric acid aqueous solutions as a function of sulfate molarity and percentage of sulfuric acid. The results from the calculations suggest that for ambient ammonia concentrations less than 10 ppb, acid sulfate aerosols are not completely neutralized.
Key concepts: Sulfuric acid, Ammonium sulfate, Ammonia, Aqueous solution, Salt (chemistry), Sulfate, Vapor pressure, Chemistry