Wp. Hamilton et Ar. Bowers, DETERMINATION OF ACUTE HG EMISSIONS FROM SOLIDIFIED STABILIZED CEMENTWASTE FORMS/, Waste management, 17(1), 1997, pp. 25-32
The chemical form of mercury in wastes to be solidified/stabilized may
lead to volatile losses from the finished solidified/stabilized monol
ith. Elemental mercury vapor (Hg vapor) was detected in the headspace
of batch reactors that contained solidified/stabilized ordinary Portla
nd cement doped with mercuric oxide (HgO) or liquid elemental mercury
[Hg degrees(l)]. Vapor concentrations increased as a function of time
and temperature; the headspace over the HgO samples was saturated in a
bout one hour, while the samples containing Hg degrees(l) reached appr
ox. 20% of saturation in about two hours. Increased temperatures due t
o cement hydrolysis lead to increased Hg vapor evolution. Mercury soli
dified/stabilized as mercuric sulfide (HgS, black) emitted no Hg vapor
. Data for the HgO and Hg degrees(l) experiments was fit to a reversib
le first-order rate expression. Samples containing HgO displayed the g
reatest volatility as a result of the rapid dissolution of HgO and the
subsequent formation of a strong driving force across the air-water i
nterface. The evolution of Hg vapor from samples solidified/stabilized
as Hg degrees(l) is limited by mass transfer resistances that kinetic
ally limit the dissolution of Hg degrees(l) into the aqueous phase. Th
e inert character of HgS (extremely low solubility and resistance to o
xidative dissolution) prevents the evolution of detectable Hg in waste
s solidified/stabilized as HgS. The findings of these studies may be i
mportant when considering treatment and disposal scenarios for Hg-cont
aining wastes. (C) 1997 Elsevier Science Ltd.