In Situ Enhanced Source Removal
2.0 Site Characterization
2.1 Historical Data
2.1.1 Location
Hill AFB is located in northern Utah, approximately 25 miles north of Salt
Lake City and five miles south of Ogden as shown in Figure 2.1.1.1.
Figure 2.1.1.1 Location map
The Base occupies approximately 6,700 acres in Davis and Weber Counties.
The western boundary of Hill AFB is Interstate 15 and the southern boundary
is State Route 193. The northern and eastern perimeters are bounded by
the privately-owned Davis-Weber irrigation canal.
2.1.2 Description and History
As shown in Figure 2.1.1.1, Operable Unit 1 (OU 1) shown in Figure 2.1.2.1
is located near the northeastern boundary of Hill AFB and consists of the
following disposal sites:
Figure 2.1.2.1 disposal sites at OU1
Chemical Disposal Pits (CDPs) 1 and 2: An industrial liquid waste disposal
site in operation from 1952 through 1973 (Montgomery, 1992). Wastes (principally
petroleum hydrocarbons and spent solvents) were burned periodically at
these sites. These are the two yellow regions inside the magenta region
of Figure 2.1.2.1.
Landfill 3 (LF 3): An industrial (dump and burn) liquid and solid waste
disposal site in operation from 1940 through 1978. Materials disposed at
LF 3 included unidentified chemicals, industrial sludge, waste solvents,
and residues from solvent cleaning operations.
Landfill 4 (LF 4): A trench-and-fill sanitary refuse landfill in operation
from 1967 through 1973. LF 4 received domestic and construction refuse,
and industrial waste consisting of drying-bed sludge, sulfuric acid, chromic
acid, and methyl ethyl ketone.
Fire Training Area 1 (FTA 1): Used by Hill AFB until 1973 as a practice
area to extinguish simulated aircraft fires. Fuels burned at FTA 1 include
jet fuel, oil, and combustible waste chemicals.
Fire Training Area 2 (FTA 2): Used by Hill AFB from 1973 until the present
as a practice area to extinguish simulated aircraft fires. Only on-specification
jet fuel or, more recently, propane, have been used in the fire training
exercises at FTA 2.
Waste Phenol/Oil Pit (WPOP): A brick-lined pit used periodically from
1954 through 1965 to dispose and burn waste oil and phenol. During excavation
of Pond 10 at OU 1, soil at the WPOP that appeared contaminated was excavated
and placed under the cap that covers LF 3.
Waste Oil Storage Tank (WOST) Site: Four 25,000-gallon, above-ground
storage tanks used to store fuel oil, jet fuel, and hydraulic oil; removed
in 1985.
2.2 Geologic and Hydrogeologic Setting
2.2.1 Topography
Hill AFB is on a terrace of the Weber Delta approximately 300 feet above
the Weber River Valley floor. The valley runs east-west immediately north
of Hill AFB. The delta surface slopes to the west and has slight to moderate
relief with elevations varying from approximately 5,045 feet relative to
the national geodetic vertical datum of 1929 (NGVD) along the eastern boundary
of Hill AFB to 4,600 feet along the western boundary. The elevation at
OU 1 is approximately 4,800 feet. The escarpment at OU 1 has moderate to
steep slopes toward the Weber River Valley. About four miles to the east
of Hill AFB, the Wasatch Mountains rise abruptly from the valley floor
to an elevation of over 9,500 feet. The Great Salt Lake lies approximately
12 miles west of Hill AFB and its current (1995) elevation is 4,200 feet.
2.2.2 Geomorphology and Geology
The subsurface stratigraphy at OU 1 can be characterized as follows: (1)
Upper Sand and Gravel Unit: An upper unit consisting of fine to coarse,
clean to silty sand interbedded with gravel that ranges in thickness from
zero to 62 feet and averages 30 feet. The lower 3 feet of this unit generally
are water bearing, although the saturated thickness ranges from zero to
10 feet. (2) Silty Clay Unit: An intermediate unit primarily consisting
of silty clay interbedded with fat clay and silt, and containing thin stringers
(tenths of inches to a few inches thick) of very fine sand. The unit is
approximately 200 feet thick and appears to be saturated with intermittent
saturated sand stringers from its top to as deep as it has been penetrated
by drilling (approximately 150 to 200 feet into the clay). (3) Deeper Sand
Unit: A possible deeper unit of unknown thickness consisting of clean sand
with occasional stringers and interbeds of silty to fat clay.
2.2.3 Hydraulic Characteristics of the Shallow Aquifer
The potentiometric surface of the shallow, unconfined on-Base aquifer slopes
to the north-northwest toward the Weber River Valley, and appears to have
remained relatively constant during several years of monitoring. The apparent
horizontal gradient is relatively flat on the OU 1 bench and in the Weber
River Valley, and relatively steep on the escarpment.
The saturated portion of the upper sand and gravel unit on Base has
a horizontal hydraulic conductivity ranging from 10-1 to 10-2 cm/sec based
on aquifer test data, and from 10-2 to 10-5 cm/sec based on slug test data.
The horizontal hydraulic conductivity of the underlying clay unit ranges
from 10-4 to 10-5 cm/sec based on slug test data. The calculated average
linear horizontal velocity of on-Base ground-water ranges from 310 to 4,656
feet per year (average of approximately 1950 linear feet per year) in the
upper sand and gravel unit, and from 0.4 to 50 feet per year (average of
approximately 10 feet per year) in the clay unit. The vertical hydraulic
gradient of the shallow on-Base aquifer in November/December 1994 ranged
from 0.05 foot/foot (ft/ft) upward to 0.9 ft/ft downward with an average
vertical hydraulic gradient of 0.25 ft/ft downward.
The vertical hydraulic conductivity of the clay unit ranges from 10-5
to 10-8 cm/sec and averages less than 10-7 cm/sec based on constant-head
permeability testing of core samples collected from the unit. Average linear
vertical velocities in the clay range from 0.014 to 0.240 feet per year
based on the vertical hydraulic conductivities, vertical gradients, and
an assumed porosity for the clay of 50 percent (Freeze and Cherry, 1979).
These results imply that, although the shallow on-Base aquifer has a downward
vertical hydraulic gradient into the clay unit, the primary component of
shallow ground-water flow is horizontal because it is easier for the ground
water to flow horizontally in the sand and gravel unit than vertically
into the silty clay unit.
2.3 Contaminant Composition and Distribution
The following paragraphs summarize the current understanding of the distribution
of contaminants at OU 1. Based on the available data, the current principal
contaminant sources at OU 1 are the contaminated soils in the vadose zone
underlying the disposal sites, the residual- and free-phase LNAPL in the
capillary fringe, and the contaminated aquifer matrix soils at and downgradient
of CDPs 1 and 2, FTA 1, and the western part of LF 3. The contaminants
include VOCs, BNAEs, PCBs, dioxins, and furans. The following paragraphs
discuss contaminant types and distribution in the various media at OU 1,
and focus on the area adjacent to CDPs 1 and 2 where this study is performed.
2.3.1 LNAPL and Soil Contamination
Based on the history of the OU 1 disposal sites (Montgomery, 1992, 1993),
bulk quantities of liquid wastes were disposed and periodically burned
at the CDPs. The waste mixture combined with the burning activities
created a very complex NAPL. Some of the components in this mixture
appear to have coated the soil particles changing the soil from a hydrophilic
material to a hydrophobic material. This apparent transformation makes
it more difficult to extract the contaminants of interest. During
previous drilling operations, a distinct "black or oily" layer with a strong
hydrocarbon odor was observed in most boreholes associated with the CDPs.
The layer was encountered just above and/or below the water table, at elevations
ranging from approximately 4,768 to 4,780 feet NGVD (i.e., 9 to 31 feet
below ground surface (bgs). The thickness of the layer ranged from approximately
1 to 10 feet, and the layer generally ended at the contact between the
sand and gravel unit and the silty clay unit. Stained soil was observed
in the silty clay unit in several boreholes, but the staining extended
less than two feet into this unit. The variation in thickness of the stained
layer probably results from variability in soil types, proximity to source,
frequency with which contaminants were dumped into the soil, and smearing
caused by seasonal fluctuations of the water table. The ground-water elevation
at the CDPs fluctuates from approximately 19 to 24 ft bgs. Hydrocarbon
staining was observed in sand stringers in the silty clay unit down to
an elevation of approximately 4,762 feet (25 to 37 feet bgs) in boreholes
associated with the CDPs (U1-129 through U1-133A, and U1-732).
In several soil borings associated with the CDPs, a distinct fuel layer
was observed above the black layer. The layer consisted of soil visibly
coated with a substance that had a strong fuel odor. This substance caused
a sheen on the soil particles, but did not discolor or stain the soil.
The fuel was observed in the sand and gravel unit at elevations ranging
from approximately 4,775 to 4,785 feet (12 to 27 feet bgs). The apparent
thickness of the fuel layer varied from approximately 3 to 10 feet. This
fuel layer probably represents LNAPL saturation in the soil above the water
table.
Based on laboratory analyses (Montgomery, 1992, 1993), the LNAPL is
composed primarily of jet fuel; however, other contaminants that have been
disposed at OU 1 have solubilized and accumulated in the LNAPL due to co-solvency.
VOCs, BNAEs, pesticides, PCBs, dioxins, and furans have been detected in
the LNAPL associated with CDPs 1 and 2. Compounds detected in the LNAPL
and their concentrations are summarized in Table
2.3.1.1.
Recently (HAFB, 1998), Hill Air Force Base has concluded, based on risk
factors, areas where it considers the soils to be contaminated and areas
where it considers the soils to present an environmental risk. These
areas are delineated in the soil
contamination map . The southern point of the area indicated
by WP002 is centered between the test cells used for surfactant mobilization
and macromolecular solubilization. The center of the northern point
of the area indicated by WP002 is slightly south of the test cell used
for cosolvent solubilization. Contamination levels in surfactant
mobilization and macromolecular solubilization were significantly higher
than the remainder of the test cells in study presented in this document.
In the current study, core samples were analyzed for decane as well
as other compounds frequently found at OU1. Geostatistics, discussed
later, were used to map the distribution of decane in the study area. The
results
of this analysis are shown based only on the samples collected from within
the test cells. The decane distribution shows the site contamination
is heterogeneous for this portion of OU1.
2.3.2 Ground Water
During Phases I and II of the Remedial Investigations (Montgomery 1992,
1993) and the quarterly monitoring program, 27 wells in the CDP area on
Base and on the hillside downgradient of the CDPs were sampled. Table
2.3.2.1 summarizes the concentration ranges for analytes detected in
samples from the wells. Generally, the types of compounds identified in
the ground water at the CDPs are consistent with the history of disposal
activities in the area. The majority of the wastes disposed in this area
were spent chemical solvents and petroleum hydrocarbons.
Chlorinated hydrocarbons are the most common contaminants detected in
the ground water at the CDPs. The VOC detected at the highest concentration
and with the widest distribution is 1,2-DCE. Chlorinated benzene compounds
were detected over a wide area and in relatively high concentrations, although
their distribution is much more limited than that of 1,2-DCE. The chlorinated
benzene compounds detected include chlorobenzene, 1,4-dichlorobenzene,
1,2-dichlorobenzene, and 1,2,4-trichlorobenzene. Hill AFB has prepared
a map, in their Environmental Restoration Management Action Plan May 1998,
of the dichloroethane
contamination OU1. The areas labeled WP002 are the same
as the Chemical Disposal Pits shown in yellow surrounded in magenta in
Figure 2.1.2.1.
2.4 Characterization Methods
2.4.1 CPT
Cone Penetrometer Technology (CPT) was used extensively at Hill AFB to
install sampling and monitoring equipment in the pilot treatment systems.
The CPT has advantages in being able to place instruments in the ground
with minimal disturbance and without producing waste cuttings. At
Hill AFB, a 1.75" O.D. rod with a 1" I.D. was used to install multilevel
samplers, oxygen sensors, thermocouples, and TPH sensors. The formation
at Hill was not conducive to collecting core samples with the CPT due to
the large cobbles which commonly plugged the core barrel making the core
recovery unacceptable. In addition to instrument installation,
the CPT was used to collect more traditional geotechnical measurements,
including: tip and sleeve resistance, pore pressure, and resistivity.
These measurements were used to locate the clay interface, define the stratigraphy,
and map the NAPL distribution.
2.4.2 LIF
Laser Induced Fluorescence (LIF) uses a light source on the surface connected
to a fiber optic cable to transmit light down into the profile through
a sapphire window into the soil. The light excites organic compounds
having a ring structure, causing them to emit light at a higher wavelength
(fluoresce). Thus, a fluorescence response is an indicator
of the presence of these compounds and can be used to map the vertical
and areal extent of contamination.
2.4.3 Cores
Soil cores are effective methods for characterizing contaminants in a particular
soil sample. A soil sample typically represents only a very small portion
of the total potential volume of the subsurface under investigation. Therefore,
a large number of soil cores are necessary to develop statistical confidence
in the total mass or the spatial distribution of a particular contaminant
in the system. In addition, for sites where the contamination is a complex
mixture of chemicals like the NAPL at OU 1, it is extremely difficult,
if not impossible, to identify all of the individual constituents.
Quantifying the total mass of the contaminants in the mixture is even more
difficult.
Transects of soil cores were taken in each of the test cells before
and after the remedial activities. These cores were extracted in the field
and then analyzed in the laboratory for selected target analytes. Results
were reported on a mass/mass soil concentration. Target analytes shown
in Table 2.4.3.1
were selected as major components of different classes of chemicals which
could be analyzed. Approximately eight cores were taken from each test
cell. Soil samples were taken at approximately 30 to 60 cm vertical intervals
in the treatment zone or when there was an obvious change in the stratigraphy
or level of contamination. Samples were taken throughout the contaminated
portion of the profile based on either visual detection of the contamination
or PID readings above background. Core samples were collected with a hollow
stem auger (HSA).
Figure 2.4.3.1 NAPL thickness estimated from core and LIF data.
Combining the LIF data with the core data, it is possible to generate
a map of the approximate thickness of the NAPL (Fig 2.4.3.1).
In general, the thickness of the NAPL-contaminated zone increases from
north to south over the study site. Additional data to better define
the southern limits of the NAPL smear zone would be needed to generate
a defensible estimate of the total NAPL volume. During our investigation,
we did not have permission to collect samples outside the locations presented
here. Combining core and LIF data to estimate contaminant mass for this
site is problematic. For core samples, NAPL mass was inferred from
the selected target analytes; whereas, NAPL mass is based on the presence
of fluorescing compounds for the LIF data. Data presented here
suggest inconsistencies between the core and LIF data.
2.4.4 Ground-water Sampling
Cleanup standards are often based on potential exposure by ingestion of
drinking water. Thus, knowing the activity of regulated compounds in the
ground water before and after remediation gives a good indication as to
the immediate hazard through the ingestion route but gives no indication
as to the mass of water which might be impacted at this level by dissolution
from the source. Each of the test cells had twelve multilevel samplers
and each of the samplers had five or more sampling points. The multilevel
samplers were vertically positioned within the zone targeted for remediation.
In addition to the multilevel samplers, samples were collected from seven
injection/extraction wells which were screened throughout the target zone.
These sampling points were analyzed for target constituents before and
after remediation to evaluate where and how much improvement in the solution
concentration was observed.
2.4.5 Ground-penetrating Radar
Two surveys were performed using ground-penetrating radar (GPR) to assist
in determining the depth to clay. The primary purpose was to assist
in the design of the test cells which were constructed of sheet piles driven
into the clay to hydraulically isolate them from the surrounding aquifer.
The first survey was performed around cell f (cosolvent solubilization)
which was the first cell constructed. This survey was very successful
in delineating the depth to clay(Young and Sun, 1996). The survey
was calibrated with several CPT determined clay interface depths.
It was decided to move the remainder of the study south of the first study.
Thus, a second survey (Young and Sun, 1998) was performed in a fenced area
at the site of a former lined evaporation pond and the site of one of the
chemical waste pits see
Figure
2.1.2.1 . There were numerous interferences with man-made objects
in the second survey. The results of the second survey which were
performed prior to the installation of the test cells are shown in Figure
2.4.5.1. The actual cell installation was completed prior to
the completion of the radar data analysis. For a more complete description
of the GPR survey, see Young and Sun, 1996, 1998.