The fate of combustion-generated polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated
dibenzofurans
(PCDFs) captured in sorbent-based, air pollution control
devices remains uncertain. This process was simulated
by
passing vapor-phase 1,2,3,4-tetrachlorinated
dibenzo-p-dioxin (TCDD) to a fixed-bed reactor laden with, typically,
1
g of calcium (Ca)-based sorbent. The sorbent bed,
reactor
rinsate, evaporation chamber, and gas impingers were
analyzed separately to balance and account for the TCDD
input. Tests at 160−300 °C demonstrated 50 to
100%
conversion of TCDD to higher molecular weight, chlorinated
products with both aromatic and aliphatic components.
The unlikeliness of conventional semivolatile GC/MS
analyses
to detect these higher molecular weight products may
offer an alternative explanation for research studies
citing
destruction or volatilization of chlorinated organics in
the
presence of Ca-based sorbents. The applicability of
this
reaction to other halogenated organics, such as polychlorinated biphenyls, may provide a method for
contaminated
soil treatment. More extensive experimental and
analytical
work is necessary to fully understand the reaction
mechansim, the full range and stability of potential
reaction
products, and the ecological and human health
implications.
Alteration of the structural symmetry and size of the
TCDD
molecule (and related halogenated organics) will likely
cause significant reductions in
toxicity.