exception of total xylenes, volatile organic con-
tar samples (Table 4). Because of the variability,
centrations were higher in treated than in un-
there is no statistically significant difference in the
treated samples. Elevated levels of ketones may
samples before and after treatment. Conversely,
be the result of in-situ oxidation of corresponding
when the TCLP results are examined, there is a
alcohols present, but not analyzed for, in the
slight increase in the total leachable TPH in the
starting material.
samples after treatment (Table 5). Here again, the
Increasing organic concentrations runs
increase in leachability is believed to be due to the
counter to the basic principle of the DCR process
increase in surface area associated with the finely
that is designed to encapsulate organics render-
dispersed DCR product compared to the hard
ing them less available. We believe that this out-
and almost intractable obsidian-like tar lumps in
come was caused by two factors. One, the mixing
the starting material. This leachability would be
process broke up the tar masses greatly increas-
significantly lower in hard compacted DCR soil
ing contact surface areas for the extracting solu-
bodies, as in subgrade for parking areas or road
tions. Two, the hydrophobic CaO never properly
construction, compared to the loose, fine product
dispersed into the asphalt tar because at the pre-
subjected to TCLP testing in the laboratory.
vailing field temperatures (< 0C), the asphalt tar
In contrast to the solid asphalt tar, the other
was a solid. The heat of mixing was insufficient
generally led to large decreases in organic con-
phase prior to the hydration reaction. Under cold
centrations following DCR treatment (Tables 6
climates, heating the asphalt tar prior to mixing
and 7). There were at least two reasons for this
would probably lead to a better DCR product.
contrast. One, the other organics were present in
Most constituents were either not detected in
the liquid state (e.g., oils, greases, JP4, diesel) at
the TCLP extracts or were present at levels that
these sites which facilitates proper adsorption of
were just above the detection limits (Table 5).
the organic phase onto the hydrophobic CaO be-
There was no leachable benzene detected; when
fore the DCR reaction. Two, the other organics
other leachable aromatics were detected, they
were present at much higher concentrations ini-
were four orders of magnitude below applicable
tially for these three sites (Tables 6 and 7) com-
drinking water standards. The most water-solu-
pared to the asphalt tar site (Tables 4 and 5).
ble constituents, notably acetone and 2-butanone,
There was a dramatic reduction in the extract-
were generally only present at low ppb levels,
able TPH after DCR treatment for the Oil/Water
three to four orders of magnitude below the regu-
Separator Pond Sediments, and this presumably
latory limit for 2-butanone, the only ketone for
reflects a combination of volatilization and
Ca(OH)2 encapsulation of intermediate- and high-
which limits exist.
er-molecular-weight hydrocarbons associated
The TPH in the solid raw and DCR-treated tar
with the oils and greases released to the pond
samples is quite variable, and no doubt reflects
(Table 6). The total lower-molecular-weight (gaso-
differing amounts of small tar flakes in the soil/
Table 5. Total extractable concentrations of TPH and volatile organics in
TCLP extracts of asphalt-tar samples (mean1 SE).
Minimum
Alaska or
detectable
Federal
Compound
Units
limit
Untreated
Treated
standard
g L1
n.a.†
Acetone*
--
23
14a
156
111a
g L1
2Butanone
1.6
1.4
0.4a
6.4
1.1b
200,000
g L1
Benzene
0.63
0.3
0.0a
0.3
0.0a
5
g L1
4Methyl2pentanone
1.5
1.3
0.2a
2.2
0.4a
n.a.
g L1
Toluene
0.58
0.37
0.08a
0.40
0.11a
1,000
g L1
2Hexanone
1.2
0.6
0.0a
1.7
0.1b
n.a.
g L1
Ethylbenzene
0.56
0.28
0.00a
0.56
0.18a
700
g L1
Total xylenes
1.1
1.2
0.1a
2.4
0.4b
10,000
mg L1
TPH
--
0.73
0.02a
1.24
0.07b
n.a.
* Also detected in method blanks run with these samples.
† n.a. = no applicable State or Federal standard is set.
Statistically significant differences are designated by different lower-case letters.
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