Final Decision to Certify Hazardous Waste Environmental Technology
U.S. Department of the Navy
Site Characterization Analysis Penetrometer System with Laser-Induced Fluorometry (SCAPS-LIF)
CALIFORNIA REGULATORY NOTICE REGISTER
The California Environmental Protection Agency, Department of Toxic Substances Control (DTSC) has made a final decision to certify the following company's hazardous waste environmental technology listed below:
Chapter 412, Statutes of 1993, Section 25200.1.5., Health and Safety Code, enacted by Assembly Bill 2060 (Weggeland) and effective January 1, 1994 authorizes DTSC to certify the performance of hazardous waste environmental technologies. Only technologies that are determined not to pose a significant potential hazard to the public health and safety or to the environment when used under specified operating conditions and which can be operated without specialized training and with minimal maintenance may be certified. Incineration technologies are explicitly excluded from the certification program.
The purpose of the certification program is to provide an in-depth, independent review of technologies at the manufacturer's level to facilitate regulatory and end-user acceptance and to promote and foster growth of California's environmental technology industry.
DTSC makes no express or implied warranties as to the performance of the manufacturer's product or equipment. The end-user is solely responsible for complying with the applicable federal, state, and local regulatory requirements. Certification does not limit DTSC's authority to require additional measures for protection of public health and the environment.
By accepting certification, the manufacturer assumes, for the duration of certification, responsibility for maintaining the quality of the manufacturered equipment and materials at a level equal or better than was provided to obtain certification and agrees to be subject to quality monitoring by DTSC as required by the statute under which certification is granted.
DTSC's notice to certify was published in the California Regulatory Notice Register Volume 96. The DTSC's final certification shall be effective from August 5, 1996 to August 5, 1999.
Additional information supporting DTSC's final certification decisions is available from:
The final certification statement and the certification limitations for the technology follows:
U.S. Department of the Navy
Certification Statement and Technology Specifications
Under the authority of Section 25200.1.5 of the California Health and Safety Code, DTSC hereby certifies the NRaD SCAPS-LIF technology as a Site Characterization technology when operated, monitored, and maintained according to NRaD's protocols and specifications subject to conditions specified in this certification. The method is an in-situ field screening technique for characterizing the subsurface distribution of POL contamination prior to the installation of monitoring wells or soil borings. As a field screening method, it is not a replacement for soil sampling borings and monitoring wells; but is a means of reducing the number, and improving the placement, of borings and monitoring wells required to achieve site characterization. The method provides field screening data on the in-situ distribution of POL products indirectly from the fluorescence response induced in PNAs when the PNAs are components of the POL products; the most effective fluorescence response is obtained for POL products containing PNAs with three or more aromatic rings. The method detects PNAs in the soil matrix throughout the vadose, capillary fringe and saturated zones. The method provides a "detect/non-detect" field screening capability relative to a specified detection limit derived for a specific fuel product in a site-specific soil matrix. For each specific site, calibration procedures are required to determine a fluorescence threshold and corresponding site detection threshold, typically in terms of mg/kg Diesel Fuel Marine (DFM). The detection threshold is subsequently applied to TPH or TRPH data for parallel soil boring samples to classify each into a "detect" or "non-detect"category. Site-specific detection limits typically vary from levels equivalent to approximately 100 mg/kg Total Petroleum Hydrocarbons (TPH, Modified EPA Method 8015) or Total Recoverable Petroleum Hydrocarbons (TRPH, EPA Method 418.1) to over 1000 mg/kg TPH or TRPH. Direct comparisons of sensor data with TPH or TRPH laboratory data for field-selected, non-random samples, collected using a split spoon sampler by boring over and adjacent to the SCAPS push hole with a conventional hollow-stem auger, show approximately 85% agreement when using the "detect/non-detect" criteria determined for each site.
Although the sensor provides a nearly linear numerical response over a dynamic range of approximately three orders of magnitude starting from a minimum detection capability as low as 10's of ppm (weight of POL product /weight soil), the certification is limited to a qualitative field screening method because sensor response has been shown to be very site specific, and vary as a function of the soil type as well as the composition of the petroleum hydrocarbon residual being investigated. In addition, varying background concentrations of naturally occurring fluorescing compounds can produce matrix interferences.
Qualitative use of spectral data provides a means of distinguishing different POL products associated with fluorescence events at different depths. Spectral differences can also be used as a means of minimizing potential false-positives arising from non-POL fluorophores. The technology is capable of making measurements from the ground surface to depths of 150 feet, when the sensor is used in conjunction with an "industry-standard" 20 ton penetrometer push vehicle. However, maximum depth of operation is governed by site-specific stratigraphy and the method is limited to sites where the cone penetrometer can be pushed to the depth of concern, through primarily unconsolidated sedimentary deposits or formations. Standard data collection rates (a composite measurement every 2 seconds) provide a vertical spatial resolution of better than 4 cm for a standard push rate of 1 m/min.
Limitations of Certification
DTSC makes no express or implied warranties as to the performance of the SCAPS-LIF site characterization technology. Nor does DTSC warrant that the SCAPS-LIF site characterization technology is free from any defects in workmanship or materials caused by negligence, misuse, accident or other causes.
DTSC believes, however, that the SCAPS-LIF site characterization technology can be used for field screening of hydrocarbon-contaminated sites when used in accordance with NRaD specifications and subject to the conditions specified in this certification. Said belief is based on DTSC's review of data submitted by NRaD and other pertinent information, and participation in field demonstrations.
The certification is limited to use of the SCAPS-LIF technology as a qualitative to semi-quantitative field screening method for hydrocarbon-contaminated sites. Use of the technology is limited to hydrocarbon contaminated sites where sufficient levels of PNA fluorophores are present in the hydrocarbon matrix to exhibit significant fluorescent responses at the 337 nm excitation wavelength which are above and distinguishable from background fluorescence levels. The technology has been shown to be applicable to a variety of sites contaminated by POLs, including diesel fuel marine, diesel no. 2, JP-5, and unleaded gasoline. Each site and contamination problem must be assessed for applicability by both site-specific calibration procedures and confirmation boring samples. The technology has not been shown to be applicable, for instance, to JP-4 contamination.
In its present configuration, the method cannot be used for direct detection of non-PNA (e.g. aliphatic or single-ring aromatic) compounds. Importantly, the technology cannot directly detect the presence of BTEX compounds (e.g., benzene) or other compounds of concern which do not fluoresce in response to the 337 nm excitation energy. (Note: Lower emission wavelength lasers, beyond the scope of this certification, are being developed to extend the detection capability to BTEX.)
This certification makes no claims concerning the performance or effectiveness of the SCAPS-LIF site characterization technology to quantify the concentration of petroleum hydrocarbon contamination in the subsurface or to detect specific contaminants of concern, such as benzene or other BTEX compounds. DTSC does not know all of the possible combinations of hydrocarbon products and site lithologies to which the technology may be applied, nor does DTSC know all of the performance specifications required by end-users. Achieving performance specifications involves many variables including the type and amount of contamination, the subsurface hydrogeologic conditions, presence of naturally occurring fluorophores, and other potential interferences. The applicability of the technology to a specific site depends on the contaminant concentration of concern and the site-specific detection limit determined for the site. The ability to detect the presence or absence of bulk hydrocarbon contamination (TPH or TRPH) at concentrations of concern is very site specific. Detection limits will vary as a function of the petroleum hydrocarbon contaminants, site specific lithology, and other matrix effects such as the presence of interfering fluorophores. Petroleum hydrocarbons vary significantly in composition from product to product and with weathering or decomposition in the subsurface. The characteristics of the fluorescence emission can vary significantly depending on the specific product released into the environment and the degree of degradation due to physical, chemical and biological processes. The intensity of the fluorescence emission response of a given hydrocarbon contaminant has been found to correlate inversely with the surface area of the media (e.g., sands versus clays). Vertical variations in lithology at a given site can result in variations with depth in the detection capability of the technology. Naturally-occurring non-POL fluorophores in the formation under investigation can potentially cause interferences resulting in elevated detection limits. In many cases, such as for carbonates present in soils, it may be possible to distinguish the spectral response of the natural fluorophore from those of the hydrocarbon contaminants.
Site Detection Limits and Fluorescent Thresholds determined through pre-deployment calibration procedures may not be representative of all matrices and contaminants encountered at a given site. The predeployment calibration procedure usually relies on a near-surface soil sample spiked with diesel fuel marine (DFM) or other suitable calibrant throughout a range of concentrations. If major lithologic changes exist at a site, either vertically or areally, or different contaminants are present, calibration results may not be applicable for the entire site. The fluorescence spectral response and background level fluorescence of the soil used to prepare the calibration samples should be compared to the spectral response and background level fluorescence obtained throughout the SCAPS-LIF site investigation. Depending on the specific application, improved calibration accuracy may be achieved by employing a post-investigation calibration that makes use of soil samples collected from the major lithologic unit(s) encountered at the site.
The use and performance of the standard geophysical Cone and Friction-Cone Tests (ASTM method D 3441-86) or other sensors which could be deployed with the SCAPS are not a part of this certification. However, use of the LIF sensor in conjunction with these or other sensors that can be deployed with the cone penetrometer to make parallel or concurrent measurements is neither precluded nor reviewed by this certification. Note: Caution should be used when interpreting the results of standard cone penetrometer geophysical measurements in POL-contaminated areas. Based on results of the field demonstrations, it appears that geophysical results may not be accurate in POL contaminated areas, possibly due to the lubricating properties effect on sleeve friction measurements.
Certification of the SCAPS-LIF technology is subject to the following conditions:
Basis for Certification
The certification evaluation included a review of peer-reviewed publications and other literature which describe the scientific principles upon which the technology is based and the results of studies conducted by NRaD and other researchers during the technology development process; an analysis of data from previous field studies completed by the developer at a variety of sites; participation in two detailed field demonstrations of the technology; and observations of the technology in operation at other sites. Detailed results of the certification evaluation are presented in the draft DTSC Certification Evaluation Report for this technology.
The principles of UV fluorescence of PNAs are well established in the scientific literature. UV fluorescence is used in a variety of standard test methods for analysis of PNAs, such as US EPA SW-846 Method 8310. Standard UV fluorescence analytical procedures are for aqueous or liquid phase analysis. For soils, a solvent extraction step is required prior to analysis. The innovative aspect of the Laser-Induced Fluorescence sensor is the ability to make direct measurements of PNA-containing POL contaminants in soil without the need to obtain or extract a soil sample.
As part of the certification application, NRaD provided 15 papers and journal articles which presented results from a number of engineering, research, and development studies conducted by NRaD and other researchers related to the use of the SCAPS-LIF sensor for detection of petroleum hydrocarbons in soil. These studies reported on the development and optimization of the technology, and described the results of investigations into potential concerns and other issues related to the application of the technology. A number of studies focused on identifying the effect of various properties associated with different classes of soils or sediment types (e.g., pure sands versus pure clays versus mixtures) that may affect detection limits and variations in response to DFM and other fuel types. Factors investigated included available surface area, grain size distribution, mineralogy, percent soil moisture and water saturation, and degree of soil aggregation. Emission spectra/peak maxima characteristics of various fuels/POLs were investigated to identify spectral responses and key spectral features. Various fuel types were analyzed to determine the concentrations of PNA compounds present which contribute to the overall fluorescence emission spectra of these fuels. The inability of the 337 nm laser configuration of the technology to directly detect BTEX was documented. Tests were performed which suggest that only the contaminant on or in interstices between the first layer of grains against the sapphire window contributes to a measurable florescent signal. The effect of fiber optical geometry and transmission characteristics were assessed to optimize and engineer for instrument sensitivity and performance. Various calibration procedures and standards were tested and evaluated.
Previous Field Validation Studies
Data were provided from NRaD's field validation studies, conducted at eight sites in California and one site in Arizona, with varying geologic conditions and contaminants. The lithology at these sites could be generally classified as unconsolidated sedimentary formations, primarily layers, mixtures, and combinations of sands, silts, and clays with minor occurrences of interbedded gravels. Groundwater was encountered at 6 of the sites where the depth to water table ranged from 4 to 79 feet below ground surface. Contaminants included diesel, JP-5, waste motor oil, refinery waste, oil field diluent, and unleaded gasoline. DFM was used as the daily calibration standard to determine the site detection limit and corresponding fluorescence threshold at seven of the sites. At two of the sites, Diesel No. 2 and oil field diluent were used as calibration standards. At the one site which was contaminated with unleaded gasoline, calibration was performed months after field operations were completed using a different probe. Based on these calibration data, detection limits and fluorescence thresholds for the sites ranged from 90 to 1,141 mg/kg and 106 to 199,953 fluorescence counts (arbitrary units), respectively.
Between 16 and 45 cone penetrometer pushes using the SCAPS-LIF, along with from 3 to 8 confirmation soil sampling borings, were completed at each of the study sites. Each confirmation soil sampling boring was located within a few inches of a cone penetrometer push hole such that the auger blade would overbore the push hole and that soil core samples could be obtained within several inches of the fluorescence measurements. A total of approximately 188 samples from 44 sampling borings were analyzed using EPA Method 418.1 for TRPH and modified EPA Method 8015 for TPH. These results were compared to fluorescence response results obtained from the co-located cone penetrometer push holes over the same depth intervals as the soil samples, and to the respective site-specific detection limits and fluorescence thresholds. The calibrants used to prepare the SCAPS calibration soil samples, typically DFM, were different than the calibrants used for standard TPH analyses of confirmation soil samples from these sites. Fluorescence response results were considered false positives when the fluorescence reading was greater than the established fluorescence threshold but the TPH or TRPH soil sample result was less than the site detection limit; and false negatives when the fluorescence reading was less than the established fluorescence threshold but the TPH or TRPH soil sample result was greater than the site detection limit. For the 164 TPH analyses completed there were 9 (5.5%) false positives and 12 (7.3%) false negatives. For the 164 TRPH analyses completed there were 6 (3.7%) false positives and 16 (9.8%) false negatives.
For several of the validation studies confirmation core samples were analyzed using EPA Method 8270 with tentative identification of additional peaks to determine what PNA compounds were present and to assess their relative contribution to the fluorescence emission spectra encountered at these sites. Significant concentrations of multi-ringed PNAs which are known to fluoresce were found to be present in the samples but a significant correlation between their concentrations and the fluorescence emission spectra could not be definitely established.
An unknown level of uncertainty exists in comparing fluorescence results with soil sample results due to the fundamental differences between SCAPS-LIF and the other methods. For example, the confirmation soil core samples are horizontally offset from the corresponding LIF probe push hole. There is an inherent uncertainty in determining the exact depth of a drill hole sample due to potential errors in measurement, soil sloughing, and, near the groundwater table, heaving sands. There is also an inherent difference in the soil that the LIF probe senses versus the soil core sample obtained for confirmation analysis. The LIF probe only senses fluorescence properties of the surficial layer of soil contamination adjacent to the probe's sapphire window. The TPH and TRPH analyses use only small aliquots (e.g., 10-30 grams) of soil from soil cores. Although fluorescence response signals are integrated over the "same" depth interval as the confirmation soil sample, and the confirmation core samples are homogenized prior to analysis, the two sampling systems may not be viewing the same soil, particularly where soil and contamination heterogeneities are present or where complete homogenization is difficult. Therefore, the comparison of the fluorescence response results to soil sample results may not be amenable to detailed statistical analyses, but should be considered a good indicator of the technology's performance.
The certification evaluation included two detailed field evaluations/demonstrations of the SCAPS-LIF technology, the first at a fuel storage tank farm site with Diesel Fuel Marine (DFM) contamination in Port Hueneme, California, and the second at a diesel no. 2 fuel oil spill at an active tank farm (Site 190) at Sandia National Laboratories in Albuquerque, New Mexico. These field demonstrations provided an independent evaluation of the technology's performance at site conditions representative of the performance claims for which NRaD desired certification. The field demonstrations augmented data from the field studies at other sites which NRaD had previously conducted and submitted in support of certification. The final work plans for conducting the field demonstrations are provided in the documents entitled:
These work plans were prepared by NRaD for the U.S. EPA Consortium for Site Characterization Technology and in accordance with their draft protocol:
The work plan was jointly reviewed and approved by Sandia National Laboratories, the U.S. EPA contractor and verification entity for the Consortium, and by the DTSC AB 2060 Technology Certification Program.
Detailed results of the field demonstrations at Port Hueneme and Sandia National Laboratories will be provided in the final certification evaluation report as well as in the report to be prepared for the Consortium for Site Characterization Technology by Sandia National Laboratories. Summary results of the demonstrations are presented below.
Port Hueneme, California Demonstration
The first demonstration, conducted at Port Hueneme, California was a relatively easy test of the technology. The site was shallow (20-25 feet) with a uniform lithology of unconsolidated sands. Contaminated sand matrices generally have a higher fluorescence response than finer- grained matrices, and are relatively easy for the cone penetrometer to push through. The contamination was Diesel Fuel Marine which has an excellent fluorescence response, and was concentrated in a relatively thin layer just below the elevation of the water table. The entrapment of the light non-aqueous phase liquids (LNAPL) contamination (i.e., DFM floating product) below the water table was likely the result of a recent rise in the aquifer.
Data from other field studies submitted in support of certification relied essentially on a single laboratory to analyze confirmation soil samples. A key element of this field demonstration included analyses of split composite samples by the Department's Hazardous Materials Laboratory to independently verify laboratory analytical results of Analytical Laboratories, Inc. (ATI), NRaD's contract laboratory.
The demonstration was conducted during April and May, 1995. A total of 15 SCAPS-LIF pushes were completed along with 15 co-located confirmation sample borings from which 232 samples were collected and analyzed for both TRPH and TPH. There was excellent agreement between the results of the split samples analyzed by ATI Laboratory and the Department's Hazardous Materials Laboratory. Results from this demonstration were consistent with NRaD's previous field validation studies. The site detection limit and fluorescence threshold were determined to be 109 mg/kg DFM, and 3558 counts, respectively, based on averaging the results of daily calibration procedures from operations conducted during May 1995. The data were also reviewed with respect to the percentage apparent false positives and false negatives. For the 232 TPH analyses completed there were 29 (12.5%) true positives, 190 (82%) true negatives, 4 (1.7%) false positives, and 9 (3.9%) false negatives; and for the 232 TRPH analyses completed there were 28 (12.1%) true positives, 189 (81%) true negatives, 5 (2.2%) false positives, and 10 (4.3%) false negatives. The fluorescence response pattern with depth data for each push location was compared with the results of the co-located boring confirmation samples. With this approach there was only one apparent anomaly, as the vertical pattern of contamination determined SCAPS-LIF technology for each borehole generally matched that determined by the traditional method of analyzing core samples. The one anomaly, a false positive result from boring B10, was due to a zone of high fluorescence with peak emission spectra significantly higher than that of the DFM contamination and very similar to background fluorescence spectra.
Albuquerque, New Mexico Demonstration
A second field demonstration was conducted in November 1995 at a fuel tank farm leak site at Sandia National Laboratories, Albuquerque, New Mexico. This demonstration was to assess the technology's ability to characterize varying degrees of contamination at a site with deep vadose zone contamination. Groundwater depth in the area is approximately 500 feet with potential for perched water zones at shallower depths. The contamination was the result of a diesel fuel No. 2 leak of more than 5000 gallons which was discovered in 1991. Subsequent to the discovery, an effort was made to excavate the gross soil contamination but was discontinued when it was realized that the contamination had migrated to considerable depth. It is not clear whether the excavation was filled with only the contaminated soil that was removed or with other off-site fill material.
Within the depth investigated in this demonstration, 0 to 58 feet, the site lithology was principally very fine grained sandy silts with several thin layers of interbedded gravels. The cone penetrometer was unable to push below a depth of approximately 56 feet due to a compacted gravel layer encountered at that depth.
During the SCAPS-LIF pushes it became apparent that significant background fluorescence was present, primarily due to calcium carbonates (HCl addition to soil cores resulted in the release of carbon dioxide). In addition, significantly higher fluorescence responses due to carbonates occurred in the fill zone. Initial calibration samples were prepared using surface soils which resulted in relatively high fluorescence threshold and detection limit values, 13,317 counts and 929 ppm respectively. During the field demonstration it became apparent that the fluorescence characteristics of the shallow soil sample used to prepare the calibration samples was not representative of deeper soils below the fill. For example, consistently lower fluorescence levels were encountered during Push No. 12, a background push immediately outside the contaminated area. This issue was discussed on-site with the operator and it was agreed that it would be appropriate to use calibration samples prepared from core samples which were obtained from Boring B12 (co-located with Push No. 12) below the depth of the fill material. After the demonstration was completed, additional calibration samples were prepared using a soil core sample selected from Boring B12 which resulted in much lower fluorescence and detection thresholds, 1094 counts and 88 mg/kg DFM respectively.
The demonstration included 3 cone penetrometer pushes along with 3 co-located borings from which 92 confirmation samples were obtained for TPH and TRPH analysis. The data were reviewed with respect to the percentage of apparent false positives and false negatives based on the lower site detection and fluorescence threshold values determined for the site, 88 mg/kg DFM, and 1094 counts, respectively. For the 92 TPH analyses completed there were 68 (74%) true positives, 7 (8%) true negatives, 17 (18%) false positives and 0 (0%) false negatives; identical results were obtained using TRPH data. All of the false positives corresponded to background emission spectra encountered at the site, with peak wavelengths ranging from 475 to 500 nm versus the peak wavelength of around 415 nm characteristic of fuel products. A high number of false positives (14 of 17) occurred primarily above the fourteen foot depth within the fill material. Removing these samples corresponding to the background emission spectra gave overall results consistent with results achieved in the Port Hueneme demonstration and NRaD's previous field studies.
The data were also reviewed with respect to the percentage apparent false positives and false negatives based on the high initial site detection and fluorescence threshold values determined for the site, 929 mg/kg DFM, and 13,317 counts, respectively. For the TPH analyses completed there were 52 (56.5%) true positives, 23 (25%) true negatives, 4 (4.4%) false positives, and 13 (14.1%) false negatives; results for TRPH were similar. These results, particularly the high level of false negatives, emphasize the importance of using representative soils in preparing the calibration samples.
Field Observations at Other Sites
The certification evaluation also included observations of the technology during operations in a field screening or investigation mode at several other sites, including Naval Air Station North Island, Naval Air Weapons Station China Lake, and Marine Corps Air Ground Control Combat Center Twenty-Nine Palms. This effort provided valuable first-hand information on how the system, and its operators, perform when the technology is deployed at a site where little or no information is available on the subsurface conditions (as may be the case when the technology is used as a field screening tool). It was also important to understand how the system is routinely calibrated and operated, what difficulties different site conditions might present to the use of the technology, and how operations can be adjusted to address such unexpected difficulties.
Recommended Applications of the SCAPS-LIF System
The SCAPS-LIF system has application as a field screening technology for characterizing petroleum hydrocarbon contamination sites where the origin of the contamination is from petroleum products or wastes containing PNAs, such as diesel fuel, diesel fuel marine, bunker fuel, crude oil, refinery wastes, or unleaded gasoline. It should also have applicability at other types of sites with PNA contamination, such as manufactured gas plant sites. The lithology should be such that the cone penetrometer can penetrate the depth of concern at the site. It is intended to delineate the distribution and boundaries of the source of contamination; it is not intended to identify dilute dissolved-phase contamination plumes. If strong naturally occurring fluorophores are present at the site, it must be determined whether these may interfere with the technology's effectiveness.
The SCAPS-LIF system can provide relatively rapid, vertically-continuous, real-time in-situ analysis for the presence or absence of subsurface petroleum hydrocarbon contamination both above and below the water table. The technology can efficiently delineate the horizontal and vertical boundaries as well as the three-dimensional distribution of the contaminants in the subsurface source area. It can be used for field screening at sites where essentially no previous characterization soil borings and sampling data are available, or to further delineate the contamination at sites where some level of conventional characterization work has already been completed. The technology also has application in monitoring the stability and movement of contaminant plumes, and in monitoring the progress of in-situ remediation technologies, such as bioventing.
At sites where the technology is applicable, results of the SCAPS-LIF field screening can be used to optimize the location and reduce the number of soil sampling borings and groundwater monitoring wells necessary to characterize a site. Such decisions can effectively reduce the overall number of samples that need to be submitted for costly and time consuming off-site laboratory analyses, and the time and costs associated with multiple or iterative field investigations.
The technology is certified to provide qualitative screening level data which indicates the presence or absence of POL (Petroleum, Oils, and Lubricants) contamination in soils. There is, however, a semi-quantitative aspect to this technology; order of magnitude changes in fluorescence response at the contaminants' response wavelength generally indicate real changes in contaminant concentrations. Method sensitivity and detection limits are very site specific and depend on both the subsurface lithology and contaminant composition. Determining applicability of the technology requires system calibration with representative soil samples from the site spiked with varying concentrations of a DFM or other standard, as well as traditional confirmation boring sample analyses.
This certification is for the specific claims, conditions, and limitations outlined in this notice, and is based on DTSC's evaluation of the technology's performance. The Certification does not change the regulatory status of SCAPS-LIF technology; it should, however, facilitate and encourage the acceptance of this technology as a field screening method for site characterization, thereby reducing the number of soil sampling borings and monitoring wells, as well as the overall time and effort, required to fully characterize a site.
Use of this technology as a field screening method for site characterization does not require a hazardous waste management permit issued by DTSC. However use of the technology may be subject to regulation by other state and local agencies. For each specific application, the end-user must ensure compliance with all applicable regulations and standards established by other state and local agencies.
Duration of the Certification
This certification will remain in effect for three years from the date of issuance, unless it is revoked for cause or unless a duration for certifications different from that specified in this certification is adopted in regulations. If a different duration is specified in regulations, the duration of this certification will be that provided for in the regulations, beginning from the original data of the issuance of this certification.
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File last updated: October 25, 1996