Grantee Research Project Results
2003 Progress Report: Laser Based Studies of Atmospheric Mercury Transformation: Laboratory Kinetics and Ultrasensitive Detection of Elemental and Reactive Gaseous Mercury
EPA Grant Number: R829795Title: Laser Based Studies of Atmospheric Mercury Transformation: Laboratory Kinetics and Ultrasensitive Detection of Elemental and Reactive Gaseous Mercury
Investigators: Hynes, Anthony J.
Institution: University of Miami
EPA Project Officer: Chung, Serena
Project Period: January 1, 2003 through December 31, 2006
Project Period Covered by this Report: January 1, 2003 through December 31, 2004
Project Amount: $559,363
RFA: Mercury: Transport, Transportation, and Fate in the Atmosphere (2001) RFA Text | Recipients Lists
Research Category: Heavy Metal Contamination of Soil/Water , Air Quality and Air Toxics , Air , Safer Chemicals
Objective:
Recent observations have suggested that gas phase chemical reaction may play a role in the atmospheric transformation of mercury. The overall objectives of this research project are a series of measurements and technique developments that will allow both the chemical reactivity, atmospheric concentrations, and rates of emission and deposition of both elemental and reactive gaseous mercury to be better defined. Laboratory studies will measure the rate coefficients for the reactions of Hg(0) with the hydroxyl radical and with halogen atoms, X, and halogen monoxides, XO, where X = Cl, Br, or I. When feasible, the reaction products and their yields will be identified. Reactions will be studied under conditions that are representative of the arctic, the upper troposphere, and the global marine boundary layer. In addition, we will investigate the feasibility of laser-based excitation schemes for the rapid, ultrasensitive detection of gas phase elemental mercury and reactive gaseous mercury.
Progress Summary:
We have studied the reactions of Hg(0) with Cl and Br using photolysis of Cl2 and Br2 monitoring the decay of Cl and Br in an excess of Hg(0):
Hg + Cl + M -> HgCl + M (1)
Hg + Br + M -> HgBr + M (2)
We performed measurements at 100 and 200 Torr in N2. We saw no evidence for
any reaction within the precision of our measurements. To ensure that our experimental
approach was reasonable, we monitored the decay of Cl atoms in a known concentration
of C2H6, and we obtained good agreement with the literature rate coefficient
for this reaction. Our results suggest that the rate coefficients for reactions
(1) and (2) are slower than 5 x 10-13 cm3 molecule-1 s-1 at 200 Torr. For reaction
(1), this would give a limit of 2 x 10-12 cm3 molecule-1 s-1 at 1 atmosphere
pressure. We have photolyzed HgCl2 at 266 nm and directly monitored HgCl on
the 23/2- 2
transition. This is the first observation of this molecule using
the laser-induced fluorescence (LIF) technique. We have obtained LIF spectra
of the (0-0) and (1-0) bands. We have obtained dispersed fluorescence spectra,
pumping the (0-0) and (1-0) bandheads. In addition, this demonstrates that
we can use photofragment LIF to unambiguously monitor HgCl2. We have examined
the use of sequential two photon LIF in conjunction with preconcentration for
the detection of ambient Hg(0) and reactive gaseous mercury.
Future Activities:
We will monitor the decay of Hg(0) in an
excess of Cl and Br atoms, monitoring both species by LIF. To avoid problems
with secondary
chemistry, we will produce both Hg(0) and our free radical photolytically.
It required considerable effort to detect BrO using 2-photon LIF excitation
on the C 2 -X 2
transition at 353 nm, and we have not been able to reproduce
the results of Delmdahl, et al., and observe BrO fluorescence. One potential
problem may have been the insensitivity of our photomultiplier tube (PMT) at
the detection wavelength. We have purchased a PMT, which is similar to that
used by Delmdahl, et al., and we plan to repeat these experiments. We will
attempt to detect both HgBr and HgI using LIF on the 2
3/2- 2
transition,
using photolysis of HgBr2 and HgI2 to produce the molecules. We also will attempt
to calibrate the sensitivity of photofragment LIF for the direct detection
of HgCl2, HgBr2, and HgI2, using KCl denuders to characterize the HgX2 source
concentrations. Work on ambient detection approaches to Hg(0) and reactive
gaseous mercury will focus on improving our sampling approach to reduce our
blank signals.
Journal Articles:
No journal articles submitted with this report: View all 12 publications for this projectSupplemental Keywords:
air, ecosystem protection, environmental exposure and risk, international cooperation, pollutants, toxics, waste, air quality, atmospheric sciences, chemicals, chemistry and materials science, environmental chemistry, environmental monitoring, air toxics, mercury, Hg, air pollutants, atmospheric chemistry, atmospheric deposition, atmospheric mercury, atmospheric mercury chemistry, atmospheric mercury cycling, chemical kinetics, contaminant transport models, fate and transport, gaseous mercury, heavy metals, laser studies, mercury, mercury chemistry, mercury cycling, mercury emissions, mercury vapor., Air, Scientific Discipline, Ecosystem Protection/Environmental Exposure & Risk, INTERNATIONAL COOPERATION, Waste, POLLUTANTS/TOXICS, Fate & Transport, Air Quality, Environmental Chemistry, Chemistry and Materials Science, Atmospheric Sciences, air toxics, Chemicals, Environmental Monitoring, heavy metals, laser studies, atmospheric chemistry, atmospheric mercury chemistry, atmospheric deposition, gaseous mercury, fate and transport, air pollutants, chemical kinetics, Hg, mercury chemistry, mercury cycling, contaminant transport models, mercury vapor, atmospheric mercury cycling, mercury emissions, modeling, atmospheric mercuryProgress and Final Reports:
Original AbstractThe perspectives, information and conclusions conveyed in research project abstracts, progress reports, final reports, journal abstracts and journal publications convey the viewpoints of the principal investigator and may not represent the views and policies of ORD and EPA. Conclusions drawn by the principal investigators have not been reviewed by the Agency.