Yakima
Valley Spray Facility Cleanup
Richard H. Bassett, Washington State Dept of Ecology
Toxics Cleanup, Yakima, WA
Long
Term TCE Source Area Remediation using Short Term
Emulsified Edible Oil Substrate (EOS(R))
Recirculation
M. Tony Lieberman, Solutions Industrial &
Environmental Services, Inc., Raleigh, NC
Real-Time
DNAPL Source Delineation Using the Triad Approach
Michael A. Singletary, Navel Facilities Engineering
Command, North Charleston, SC
Surgical
Implementation of Blast Fractured Bedrock Trench
Technology at an Active Chemical Plant
Richard H. Frappa, Geomatrix Consultants, Inc.,
Amherst, NY
How
Clean Can It Get?- Critical Review of Mechanisms and
Results Achieved Using Thermal Remediation and Where You
can Go Wrong
Gorm Heron, TerreTherm, Inc., Bakersfield, CA
"Low-Quality"
Steam injection To Enhance Conventional In Situ Remedial
Technologies
Daniel Groher, ENSR International, Westford, MA
Yakima
Valley Spray Facility Cleanup
Richard H. Bassett, Washington State Department of
Ecology Toxics Cleanup Program, 15 W. Yakima Avenue, Suite
200, Yakima, WA, 98902-3452, Tel: 509-454-7839, Fax:
509-575-2809, Email: rbas461@ecy.wa.gov
A pesticide formulator-distributor, Yakima Valley Spray (YVS),
operated in Yakima, Washington from 1908 to 1974.
A large bulk fuel distributor operated immediately
next to YVS during a similar timeframe. A remedial investigation conducted on these
properties identified more than sixty contaminants,
pesticides, hydrocarbons, volatile organic compounds, and
metals that had been released to the soil and groundwater.
Nine indicator contaminants would eventually drive
the cleanup. The greatest health and environmental threats in soil and
groundwater were aldrin, dieldrin, and arsenic.
Site groundwater annually fluctuates from 13 to 21 feet below
ground surface. An
annual 60 degree direction change in flow occurs too.
From an irrigation influence, groundwater
fluctuations created a ‘smear zone’ that contributed
contaminants to downgradient receptors.
Site cleanup was complicated by contamination under
two storage buildings, under two adjacent railroad spurs,
an upgradient unknown source of perchloroethylene, a sewer
line, buried fuel tanks, and an irrigation canal.
A two-year break occurred after the remedial
investigation when the site became a Washington State
Legislature ‘pilot’ site.
The Cleanup Action Plan gave the responsible parties options
of (1) minimal excavation with long-term bioventing and
biosparging, or (2) maximum excavation to low winter
groundwater. The
parties chose maximum excavation as the cheaper
alternative and to expedite facility cleanup.
A consent decree was signed between the ten responsible
parties and the State of Washington.
Building demolition, temporary track removal, and
excavation occurred from January, 2004, to May, 2004.
Excavation and transport of about 80,000 tons of
contaminated soil to appropriate landfills occurred.
Still to be completed are two years of quarterly
confirmation samplings and analyses from 17 monitoring
wells to determine the success of the source removal.
Cleanup cost is estimated at 10-12 million dollars.
Long
Term TCE Source Area Remediation using Short Term
Emulsified Edible Oil Substrate (EOS®)
Recirculation.
M.
Tony Lieberman, RSM, Solutions Industrial &
Environmental Services, Inc., 3722 Benson Drive, Raleigh, NC 27609, Tel: 919-873-1060, Fax: 919-873-1074,
Email: tlieberman@solutions-ies.com
Dr. Robert C. Borden, P.E., Solutions Industrial &
Environmental Services, Inc., 3722 Benson Drive, Raleigh, NC 27609, Tel: 919-873-1060, Fax: 919-873-1074, Email:
rcborden@solutions-ies.com
Christie Zawtocki, P.E., Solutions Industrial &
Environmental Services, Inc., 3722 Benson Drive, Raleigh, NC 27609, Tel: 919-873-1060,
Fax: 919-873-1074, Email:
czawtocki@solutions-ies.com
Ira May, Army Environmental Center, SFIM-AEC-CDT, 5179
Hoadley Road, Aberdeen Proving Ground, MD
21010-5401, Tel: 410-436-3152,
Fax: 410-436-1548, Email: ira.may@us.army.mil
Clifton C. Casey, P.E., Naval Facilities Engineering
Command, Southern Division, 2155 Eagle Drive, North
Charleston, SC 29419-9010,
Tel: 843-820-5561, Email: cliff.casey@navy.mil
Solutions Industrial & Environmental Services, Inc.
(Solutions-IES) designed effective treatment approaches
using emulsified edible oil substrate (EOS®)
to remediate trichloroethene (TCE) source areas at two
Department of Defense installations.
Each site posed unique design challenges and
permitting constraints.
The Army Environmental Center retained Solutions-IES
to treat a 10,000 ft2 source area,
approximately 15 feet thick, at the former Tarheel Army
Missile Plant in Burlington, NC.
At this site, the low concentrations of TCE and
related contaminants were present in complex saprolite
with low well yields and subsurface structures were
located nearby. Solutions-IES’
ESTCP-funded pilot test at the Naval Weapons Station in
Charleston, SC is located in a heavily wooded area with
higher contaminant concentrations, a low yielding aquifer
and shallow groundwater gradient.
At each site, temporary recirculation systems were used to
spread EOS® throughout the desired treatment
zone. The
systems were designed to minimize operation and
maintenance needs and were effective in smearing the
substrate throughout the subsurface as evidenced by
increased levels of total organic carbon in the aquifer.
Decreased DO and ORP levels confirmed that
anaerobic reducing conditions were quickly established at
both sites. Corresponding
decreases in TCE were also observed.
At the Tarheel Army Missile Plant, TCE
concentrations were reduced from 1,690 µg/L to
non-detectable levels within 2 months of the EOS®
injection. Six
months post-injection at the Charleston Naval Weapons
Station TCE concentrations have been reduced from 18,700
µg/L to 4,300 µg/L.
The pilot tests clearly show the effectiveness of
EOS® for treating TCE-contaminated groundwater
in a variety of source area configurations.
Real-Time
DNAPL Source Delineation Using the Triad Approach
Michael A. Singletary, Southern Division, Naval
Facilities Engineering Command, P.O. Box 190010, North
Charleston, SC, 29419, Tel: 843-820-7357, Fax:
843-820-7465, Email: michael.a.singletary@navy.mil.
Michael J. Maughon, Southern Division, Naval Facilities
Engineering Command, P.O. Box 190010, North Charleston,
SC, 29419, Tel: 843-820-7422, Fax: 843-820-7465, Email:
michael.maughon@navy.mil.
Maxie R. Keisler, Southern Division, Naval Facilities
Engineering Command, P.O. Box 190010, North Charleston,
SC, 29419, Tel: 843-820-7322, Fax: 843-820-7465, Email:
maxie.keisler@navy.mil.
A focused, real-time investigation of a dense non-aqueous
phase liquid (DNAPL) source zone was conducted at the
Solid Waste Management Unit 1 (SWMU1), Naval Air Station
Pensacola, Florida. During the 1950’s and 60’s, SWMU1 received industrial
waste from painting and electroplating operations.
Chlorinated solvents, including trichloroethene (TCE),
were released to the subsurface from drying beds used to
dewater sludges generated by wastewater treatment
processes. DNAPL
is suspected to be present as disconnected residual at the
base of the unconfined aquifer at 40 to 44 feet below
ground surface. In
1998-99, approximately 10,000 gallons of hydrogen
peroxide/iron catalyst solution were injected into the
aquifer as part of a source reduction strategy to reduce
TCE levels below the default natural attenuation
concentrations established by the state regulatory agency.
Within two years of hydrogen peroxide injection,
TCE concentrations rebounded to initial levels.
Based on an evaluation of remedy effectiveness, it
appeared that poor remedy performance was due to
incomplete characterization of the DNAPL source zone as
well as the short-lived nature of the oxidant solution.
As part of an on-going optimization study of the
SWMU1 groundwater remedy, a focused characterization study
was planned using the Triad Approach as guidance.
A direct-push rig equipped with a membrane
interface probe (MIP) for DNAPL detection and an
electrical conductivity detector for soil stratigraphy
mapping was used to delineate the zone of DNAPL residual.
The
number and location of data collection points were decided
by a team of scientists and engineers as the investigation
progressed based upon the collection of real-time data and
a continuously updated conceptual site model.
Following the initial MIP survey, a mobile laboratory, capable of
producing data of quality equal to that of a fixed-base
laboratory, was used to collect confirmation samples
during the same mobilization.
By combining the use of field analytical techniques
with more traditional fixed-based laboratory methods in a
single field mobilization, the DNAPL source zone was
delineated at considerable cost savings, while still
achieving project data quality objectives.
Surgical
Implementation of Blast Fractured Bedrock Trench
Technology at an Active Chemical Plant
Richard H. Frappa, P.G., Geomatrix Consultants,
Inc., 90B John Muir Drive, Suite 104, Amherst, NY, 14228,
Tel: 716-565-0624, Fax: 716-565-0625, Email:
rfrappa@geomatrix.com
Paul F. Mazierski, Dupont Corporate Remediation Group,
Buffalo Avenue & 26th Street, Niagara Falls, NY, 14302, Tel: 716-278-5496, Fax:
716-408-9426, Email: Paul.F.Mazierski@usa.dupont.com
Craig T. Taylor, URS Corporation, 77 Goodell
Street, Buffalo, NY 14203, Tel: 716-923-1332, Fax:
716-856-2545, Email: Craig_Taylor@urscorp.com
Daniel M. Sheldon, URS Diamond, Buffalo Avenue & 26th
Street, Niagara Falls, NY, 14302, Tel: 716-278-5170, Fax:
716-408-9434, Email: Daniel.M.Sheldon@usa.dupont.com
An Administrative Consent Order (ACO) executed by the New
York State Department of Environmental Conservation (NYSDEC)
required enhancement of the hydraulic efficiency of the
existing Groundwater Remediation System (GWRS) at a large,
active chemical plant located in New York State.
A technology assessment identified groundwater
recovery from blast-enhanced fractured bedrock trenches (BFBTs)
as the preferred remedial option to improve control of a
chemical plume in approximately 5 acres of the
southwestern portion of the Plant.
BFBTs have proven to be effective in hydraulically
controlling the spread of groundwater contamination,
however, technology implementability in a chemical plant
setting in close proximity to vibration sensitive
processes and equipment owned by a business other than the
property owner presented significant technical challenges.
A Pilot Scale Technology Demonstration (PSTD) was
implemented at the Plant to demonstrate that the technique
would not only facilitate hydraulic control of
groundwater, but could be implemented safely without
impacting Plant equipment or structures.
A significant aspect of the demonstration included an
extensive assessment of peak particle velocities (PPV) and
ground vibration frequency to assess vibrations produced
by blasting. PSTD blast vibration monitoring involved: an assessment of
background vibration levels at the Plant, on-site blast
vibration level predictions produced during blasting, and
real-time monitoring of blast vibrations during the PSTD
for comparison to predicted blast vibration levels.
Real-time vibration monitoring was used to evaluate
design parameters for the blast program.
The PSTD was successful and provided information
required to implement full scale design for safe, bedrock
blasting within 25-feet of sensitive Plant chemical
operations and directly beneath high voltage power
transmission lines.
The PSTD and full-scale technology implementation produced
two, 200-foot long BFBTs.
Although originally intended as an enhancement,
analysis of hydraulic performance data indicated that
higher BFBT pumping rates may actually serve to replace
operation and maintenance (O&M) of nearly a dozen
conventional pumping wells in the existing GWRS.
Benefits of the blast-fractured bedrock trenches
include increased mass removal, more efficient formation
of continuous hydraulic capture zones, and significantly
lower O&M costs compared to the existing GWRS. This work demonstrates the safety and predictability of
detonating explosives to create blast-fractured bedrock
trenches in sensitive settings, thereby potentially
increasing use of this technology in maintaining
cost-effective, long-term hydraulic control at process
sensitive industrial operations.
How
Clean Can it Get? – Critical Review of Mechanisms and
Results Achieved using Thermal Remediation – and Where
You can go Wrong
Gorm Heron, TerraTherm, Inc., 10554 Round
Mountain Road, Bakersfield, CA 93308, Tel. and Fax: (661)
387-0610, Email: gheron@terratherm.com
Ralph S. Baker, TerraTherm, Inc., 356 Broad Street,
Fitchburg, MA 01420, Tel: 978-343-0300, Fax: 978-343-2727,
Email: rbaker@terratherm.com
John M. Bierschenk, TerraTherm, Inc., 356 Broad
Street, Fitchburg, MA 01420, Tel: 978-343-0300, Fax:
978-343-2727, Email:jbierschenk@terratherm.com
John C. LaChance, TerraTherm, Inc., 356 Broad
Street, Fitchburg, MA 01420, Tel: 978-343-0300, Fax:
978-343-2727, Email: jlachance@terratherm.com
Recently, results from sites that were heated and treated
using thermal remediation have indicated impressive
removal rates for dense non-aqueous phase liquid (DNAPL)
source zones in soil and groundwater.
Results from both a DOE site (Young-Rainey STAR
Center), and an industrial facility in the Midwest, have
been published, stating mass removal efficiencies in the
99.9 percent range. Soil concentrations below or near
non-detect are reported, and groundwater concentrations
near or below MCL have been observed inside the original
source zones. These results appear almost unrealistic,
considering the recalcitrant nature of DNAPLs in the
subsurface, long-term diffusion processes, heterogeneity
of most source zones, and frequently raised questions
about DNAPL capture at thermal sites. Other site reports,
particularly from sites where Electrical Resistance
Heating was used, have reported much less impressive
results, sometimes less than 90% mass removal. As more
data is emerging, it is becoming evident that thermal
remediation spans a wide range of heating methods, and
that applications vary from very robust, effective systems
to poorly designed and ineffective systems.
This presentation will review the mechanisms behind thermal
remediation critically, focusing on exactly what happens
at the pore and micro-scale, as well as larger scale
during heating. It will review ways for the contaminants
to be contacted, vaporized, transported under various
gradients, and show the most proper design for vapor
recovery and capture systems. Several typical design flaws
will be presented, in an attempt to explain why not all
thermal projects have achieved the success made possible
by the theory. Finally, a list of typical quality control
issues are provided – hopefully leaving the audience
with direction for better evaluating thermal remediation
proposals and applicability. The authors have worked on
approximately 20 field-scale sites where steam enhanced
remediation, electrical resistance heating, and thermal
conduction heating have been implemented.
“Low-Quality”
Steam Injection To Enhance Conventional In-Situ Remedial
Technologies
Daniel Groher, PE, ENSR International, 2
Technology Park Drive, Westford, MA, 01886, Tel:
978-589-3030, Fax: 978-589-3705, Email: dgroher@ensr.com
Timothy Adams, PG, ENSR International, 27755 Diehl Road,
Warrenville, IL, 60555, Tel: 630-836-1700, Fax:
630-836-1711, Email: tadams@ensr.com
Conventional remediation technologies such as soil vapor
extraction (SVE), multi-phase extraction (MPE), and
groundwater pump and treat can be thermally‑enhanced
to achieve remedial closure objectives that might
otherwise be infeasible or too slow.
Thermal enhancement can help mobilize light
non-aqueous phase liquids (LNAPLs) that are otherwise too
viscous to effectively recover; can increase the
volatility of target compounds to increase the mass rate
of vapor extraction; and can accelerate in-situ
biodegradation. Thermal
enhancement can be distinguished from thermal remediation
by the scale and cost of the heating processes.
Full-scale thermal remediation tends to add 100’s
to 1,000’s of kilowatt-hours of energy per cubic yard
(KWH/yd3) of soil to increase subsurface
temperatures in the treatment volume to greater than 212°F.
These high temperatures and aggressive heat input
are often required to reach very stringent treatment goals
and/or destroy contaminants in-situ, typically in
low permeability soil.
In contrast, thermally-enhanced remediations tend
to require heat inputs of 10 to 100 KWH/yd3 and
may only increase subsurface temperatures by 20° to 100°F. The lower energy input for thermally-enhanced remediation
often has lower capital and operational costs than
full-scale thermal remediation.
However, thermal enhancement is most appropriate
for a more select range of soil conditions and more
flexible remedial objectives.
ENSR has successfully applied low-quality steam (i.e., low
temperature and pressure) at three sites with heat input
less than 30 BTU/hr/yd3, including: (1) product
recovery of No. 6 fuel from a site undergoing
re-development in Massachusetts; (2) MPE remediation of
chlorinated solvents in groundwater in Illinois; and (3)
SVE of toluene and styrene in a former industrial setting
in Massachusetts. These
remedies will be contrasted with higher heat input
full‑scale thermal remediation applications.
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