Field tests on mercury speciation and emission while burning Kentucky and Illinois coals with
different chlorine contents were performed in a 100-MWe pulverized-coal boiler with low-NO
x
burners. Seven coals were used during the tests and were grouped into two sets for comparison,
with the baseline coal being shared between the two sets. The first set of four coals was used to
investigate the effect of chlorine in coal on mercury emission and its speciation by selecting coals
with similar mercury contents and different chlorine contents. The four coals in the second set
were selected to investigate the effect of mercury contents in coal on mercury emission and its
speciation by choosing coals with similar chlorine contents and different mercury contents. The
mercury concentration and speciation in the flue gas were determined using the American Society
for Testing and Materials (ASTM) standard Ontario Hydro Method (OHM) and a PS Analytical
Semi-continuous Emissions Monitoring (SCEM) system. Flue gas samplings were performed at
two locations: upstream before the electrostatic precipitator (ESP) inlet and downstream after
the ESP outlet. A thorough comparison between the two monitoring methods was made. A
sampling bias was found in the OHM sampling performed at the ESP inlet, because of the
accumulation of ash with a high carbon content on the OHM filter. An ash-free sampling probe
should be used with the OHM impinger train for obtaining accurate mercury information
whenever ash concentrations are high. Mercury emission and speciation for the seven test coals
at the ESP outlet location are described and discussed. Results indicate that the coal chlorine
content has an impact on the mercury oxidation processes, which are mitigated by high
concentrations of SO2. It is speculated that SO2 limits Cl2 formation.
The Western Kentucky University mobile laboratory for monitoring mercury emissions
measured the mercury levels in a 100-MW boiler with wall-fired low-NO
x
burners. Mercury
emissions were monitored while burning seven coals, using semicontinuous emission monitoring
at the air preheater outlet and electrostatic precipitator outlet. The collected data was then scaled
and analyzed using stepwise regression analysis. The results showed that initial mercury
concentration in the coal, as well as chlorine and sulfur levels, all influence the amount of mercury
emissions. After mercury content, chlorine had the major role in the levels of vapor-phase mercury
present in the flue gas. Chlorine promotes the chemisorption of mercury onto fly ash. Sulfur was
shown to be a major factor in the oxidation of elemental mercury but inhibited the adsorption of
oxidized mercury onto the fly ash. Further experimental results suggest that both HCl and SO2
may participate directly in the mercury oxidation mechanism.
Eight commercial fly ash samples including two from petroleum coke/coal co-firing were
characterized to determine the origin, structure, and properties of the unburned carbon. Because
of its relevance to ash utilization, the characterization included measurements of adsorptivity
toward concrete surfactants, and its dependence on carbon form, particle size, and contact time.
The coal/coke co-firing ashes are observed to possess unique optical and adsorptive properties
which are related to the size, density, and internal porosity of the coke-derived residual char.
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