Bench-scale experiments were conducted in a flow reactor to simulate entrai
ned-flow capture of elemental mercury (Hg-0) by activated carbon. Adsorptio
n of Hg-0 by several commercial activated carbons was examined at different
C:Hg ratios (by weight) (350:1-29,000:1), particle sizes (4-44 mum), Hg-0
concentrations (44, 86, and 124 ppb), and temperatures (23-250 degreesC). I
ncreasing the C:Hg ratio from 2100:1 to 11,000:1 resulted in an increase in
removal from 11 to 30% for particle sizes of 4-8 Irm and a residence time
of 6.5 sec. Mercury capture increased with a decrease in particle size. At
100 degreesC and an Hg-0 concentration of 86 ppb, a 20% Hg-0 reduction was
obtained with 4- to 8-mum particles, compared with only a 7% reduction for
24- to 44-mum particles. Mercury uptake decreased with an increase in tempe
rature over a range of 21-150 degreesC. Only a small amount of the Hg-0 upt
ake capacity is being utilized (less than 1%) at such short residence times
. Increasing the residence time over a range of 3.8-13 sec did not increase
adsorption for a lignite-based carbon; however, increasing the time from 3
.6 to 12 sec resulted in higher Hg-0 removal for a bituminous-based carbon.