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OH Radical Measurement
One way of fighting air pollution is to learn more about the Earth's natural anti-pollution defenses. A step in that direction occurred unexpectedly in the early 1980s, when former Engineering Experiment Station scientist Dr. Fred Eisele was developing a sensitive atmospheric ion-measurement technique. In the process, he discovered the technique could be adapted to measure the elusive hydroxyl (OH) radical.
Georgia Tech file photo Working at a field experiment site, GTRI scientist Dr. Fred Eisele uses a sensitive atmospheric ion-measurement technique he adapted to measure the elusive hydroxyl (OH) radical. The OH radical is considered the single most important cleansing agent in the atmosphere.
Considered the single most important cleansing agent in the atmosphere, the OH radical acts as an oxidizing agent and removes several greenhouse gases and other pollutants from the atmosphere.
Continuously replenished during the daytime, but highly reactive the molecule lasts only a fraction of a second before it combines with other chemicals and tiny even by molecular standards, the OH radical defied in situ measurement for 20 years until Eisele.
In early 1989, Eisele modified his ion-sampling apparatus to support the physical chemistry needed to detect the OH radical. His measurement technique combines the highly reactive nature of the OH radical with the extreme sensitivity offered by a mass spectrometer.
Air drawn through a sampling tube is subjected to a rapid succession of chemical reactions initiated by the addition of isotopically labeled sulfur dioxide, which converts all of the naturally occurring OH into isotopically labeled sulfuric acid. To prevent the formation of new OH by certain elements in the air sample, Eisele injects propane shortly after the initial OH is titrated away.
The acid is ionized to form an isotopically labeled bisulfate ion, which is then measured with a selected ion chemical ionization mass spectrometer. Because the OH was converted into the acid in a one-to-one ratio, the amount of sulfuric acid reveals the ambient OH concentration.
This technique also provides the unique ability to measure ambient sulfuric acid, which plays a central role in aerosol nucleation and growth in this case by detecting the non-isotopically labeled bisulfate ion. Researchers calibrate both of these measurements by photo-dissociating a known amount of water vapor with a known flux of 184.9 nanometer UV photons. Together, they form known OH and sulfuric acid concentrations in the instrument's sample inlet.
For more information, contact Dr. Fred Eisele, National Center for Atmospheric Research 1850 Table Mesa Dr., Boulder, CO 80303. (Telephone: 303-497-1483) (E-mail: eisele@ucar.edu)Last updated: October 25, 1999
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