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At least 721 records · Page 40

A Review on Adsorption Technologies for Mercury Emission Control

This study summarized existing adsorption technologies for the removal of elemental mercury in the flue gas. Both carriers (e.g., active carbon (AC), pyrolyzed char, inorganic adsorbents and fly ash) and various modification methods (pore structure improvement, oxygen-containing functional groups addition and new active reagents impregnation) were compared to shed light on the development of future adsorption technology. AC and char possibly performed more mercury adsorption capacity (MAC) compared with fly ash and inorganic adsorbents since carbon atom existence was easier to form the active halogen groups (C–X) and oxygen containing groups. Though both pore structure improvement and chemical group formation improved the MAC of adsorbents, the chemical modification methods (oxygen-containing functional groups addition and new active reagents impregnation) were more effective. The impregnation of halogen, sulfur and metal chloride could distinctly form lots of active sites on the adsorbents and developed high effective mercury adsorbents. In the future, the adsorption researches possibly focus on SO{sub 2} and H{sub 2}O resistance of adsorbents, separable adsorbents, low-cost chemical modification methods, and utilization potential of fly ash.

54 ENVIRONMENTAL SCIENCES↗

Corrosion Performance of Fe-Based Alloys in Simulated Oxy-Fuel Environment

The long-term corrosion of Fe-based alloys in simulated oxy-fuel environment at 1023 K (750 A degrees C) was studied. Detailed results are presented on weight change, scale thickness, internal penetration, microstructural characteristics of the corrosion products, and the cracking of scales for the alloys after exposure at 1023 K (750 A degrees C) for up to 3600 hours. An incubation period during which the corrosion rate was low was observed for the alloys. After the incubation period, the corrosion accelerated, and the corrosion process followed linear kinetics. Effects of alloy, CaO-containing ash, and gas composition on the corrosion rate were also studied. In addition, synchrotron nanobeam X-ray analysis was employed to determine the phase and chemical composition of the oxide layers on the alloy surface. Results from these studies are being used to address the long-term corrosion performance of Fe-based alloys in various coal-ash combustion environments and to develop methods to mitigate high-temperature ash corrosion.

36 MATERIALS SCIENCE↗

Micro- and macroscale coefficients of friction of cementitious materials

Millions of metric tons of cementitious materials are produced, transported and used in construction each year. The ease or difficulty of handling cementitious materials is greatly influenced by the material friction properties. In the present study, the coefficients of friction of cementitious materials were measured at the microscale and macroscale. The materials tested were commercially-available Portland cement, Class C fly ash, and ground granulated blast furnace slag. At the microscale, the coefficient of friction was determined from the interaction forces between cementitious particles using an Atomic Force Microscope. At the macroscale, the coefficient of friction was determined from stresses on bulk cementitious materials under direct shear. The study indicated that the microscale coefficient of friction ranged from 0.020 to 0.059, and the macroscale coefficient of friction ranged from 0.56 to 0.75. The fly ash studied had the highest microscale coefficient of friction and the lowest macroscale coefficient of friction. -- Highlights: •Microscale (interparticle) coefficient of friction (COF) was determined with AFM. •Macroscale (bulk) COF was measured under direct shear. •Fly ash had the highest microscale COF and the lowest macroscale COF. •Portland cement against GGBFS had the lowest microscale COF. •Portland cement against Portland cement had the highest macroscale COF.

36 MATERIALS SCIENCE↗

Effect of elevated temperature on alkali-activated geopolymeric binders compared to portland cement-based binders

This research focused on developing thermally-stable materials based on alkali-activation of slag, fly ash, and metakaolin compared to portland cement mixtures by using a hierarchical approach to material design. At lower length scales, X-ray diffraction (XRD) characterized the mineralogy that coupled to higher length scale experiments using thermogravimetric analysis (TGA) for determining the materials thermal stability. Additionally, high-energy X-ray computed microtomography (μCT) determined the best-performing material formulation that minimized thermal damage when exposed to high temperatures (650 °C). The thermal loading was ramped up to 650 °C from ambient temperature in 60 s and then held for a total of 10 min. The μCT identified that the alkali-activated fly ash mortar had less initial porosity than the ordinary portland cement mixtures, with more than 66% of the pores between 20 and 50 μm in diameter. Consequently, the alkali-activated fly ash mortar was able to dissipate approximately 565 °C in just 50 mm of material, outperforming all the other mixes studied in this paper with μCT confirming minimal damage after the temperature exposure.

36 MATERIALS SCIENCE↗

Degradation mechanism of blended cement pastes in sulfate-bearing environments under applied electric fields: Sulfate attack vs. decalcification

Applied electric fields, the reason behind stray currents, accelerate the ingress of sulfate into cementitious materials. To identify mitigation approaches, this study investigates the effects of slag and fly ash on sodium sulfate attacks of cement pastes under a constant electric current. The mineralogical alterations induced by the attacks were analyzed using X-ray diffractometry, thermogravimetric analysis, scanning electron microscopy, and thermodynamic modeling. The dissolution of aluminates in the slag and fly ash induced a monosulfate-rich area (>~20 mm from the cathode surface) to form next to the ettringite-rich area on the sample surface (<~20 mm). This effect reduced the availability of SO 4 2– in the pore solution, thereby hindering the penetration of sulfate. Meanwhile, the consumption of portlandite by the pozzolanic reaction lowered the decalcification resistance of the materials. This produced a wide area that endured the decomposition of portlandite and carbonate-AFm. Altogether, blending 30% fly ash did not improve the resistance of the material to either sulfate attacks or decalcification; blending 50% slag can effectively mitigate sulfate ingress, though decalcification may become a governing mechanism in the degradation process.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Performance assessment of dilute-acid leaching to improve corn stover quality for thermochemical conversion

Lignocellulosic biomass is a sustainable energy source that can help meet the increasing demand for biofuels in the United States. However, the quality and availability of such feedstocks greatly affects their suitability for downstream conversion. This work reports the effects of dilute-acid leaching at various solid loadings, temperatures and acid loadings on the quality of a traditional biochemical feedstock, corn stover, as a potential feedstock for thermochemical conversions. At 5 wt% solids, dilute-acid leaching was observed to effectively remove 97.3% of the alkali metals and alkaline earth metals that can negatively affect degradation pathways during pyrolysis and result in greater yield of non-condensable gases. In addition, up to 98.4% of the chlorine and 88.8% of the phosphorus, which can cause equipment corrosion and foul upgrading catalysts, respectively, were removed. At 25°C in the absence of acid, only 6.8% of the alkali metals and alkaline earth metals were removed; however 88.0% of chloride was still removed. The ratio of alkaline/acidic ash species has been suggested to proportionately relate to slagging in biopower applications. The initial alkali/acid ratio of the ash species present in the untreated corn stover was 0.38 (significant slagging risk). At 5 wt% solids, this ratio was decreased to 0.18 (moderate slagging risk) at 0 wt% acid and 90°C, and was decreased to 0.07, 0.08 and 0.06 at 0.5 wt% acid at 25°C, 50°C and 90°C, respectively (little or no slagging risk). Increasing the acid loading to 1.0% only slightly decreased the measured alkali/acid ratio of remaining ash species. Lastly, the results presented here show that a water wash or dilute-acid preprocessing step can improve corn stover quality for pyrolysis, hydrothermal liquefaction and biopower.

09 BIOMASS FUELS↗

Experimental study of the application of rotating fluidized beds to particle separation

Rotating fluidized beds provide a unique opportunity to exploit fluidization under higher particle forces. The centripetal force in a rotating fluid bed is typically on the order of 10 times the force of gravity. Since the force keeping the particles in the unit is larger, the drag force can also be larger, allowing for higher gas and slip velocities. This operating regime provides intensified gas-solids contact through higher mass transfer, heat transfer, gas throughput, and bubble suppression. One application for using a rotating fluidized bed is in Chemical Looping Combustion (CLC). When solid fuels are used, oxygen carrier and ash are mixed in the process. In order to maintain high carbon capture efficiencies and recyclability of the oxygen carrier, the ash needs to be separated from the oxygen carrier. This separation can be done aerodynamically since the oxygen carrier is larger and heavier than the ash. It is theorized that rotating fluidized beds could improve both the gas-solid and solid-solid separation process efficiency and throughput as compared to conventional fluidized beds. A 43 cm diameter, 2.5 cm long vortex chamber has been designed and constructed to investigate the application to particle separation. A series of experiments have been performed to investigate the separation of different binary mixtures of solids. These experiments demonstrate the use of a rotating fluidized bed for high-G intensified particle separation that can be combined with high-G intensified gas-solids contact and gas-solids separation.¼

01 COAL, LIGNITE, AND PEAT↗

Comparison of coal/solid recovered fuel (SRF) with coal/refuse derived fuel (RDF) in a fluidised bed reactor

An experimental study was undertaken to compare the differences between municipal solid waste (MSW) derived solid recovered fuel (SRF) (complying with CEN standards) and refuse derived fuel (RDF). Both fuels were co-combusted with coal in a 50 kW fluidised bed combustor and the metal emissions were compared. Synthetic SRF was prepared in the laboratory by grinding major constituents of MSW such as paper, plastic, textile and wood. RDF was obtained from a local mechanical treatment plant. Heavy metal emissions in flue gas and ash samples from the (coal + 10% SRF) fuel mixture were found to be within the acceptable range and were generally lower than that obtained for coal + 10% RDF fuel mixture. The relative distribution of heavy metals in ash components and the flue gas stream shows the presence of a large fraction (up to 98%) of most of the metals in the ash (except Hg and As). Thermo-gravimetric (TG) analysis of SRF constituents was performed to understand the behaviour of fuel mixtures in the absence and presence of air. The results obtained from the experimental study will enhance the confidence of fuel users towards using MSW-derived SRF as an alternative fuel.

01 COAL, LIGNITE, AND PEAT↗

The use of commercial and industrial waste in energy recovery systems - A UK preliminary study

Highlights: > Commercial and industrial waste samples collected. > Samples analysed for calorific value, moisture, ash and elemental composition. > Values similar to those of municipal solid waste and refuse derived fuel. > Sampled waste could be used in current energy recovery systems with minimal retrofitting. > Sampled waste could account 6.5% towards the UK's 2020 renewable electricity target if all qualifying waste is used. - Abstract: With 2020 energy targets set out by the EU fast approaching, the UK is trying to source a higher proportion of its energy from renewable resources. Coupled with this, a growing population and increasing trends in consumer demand have resulted in national waste loads increasing. A possible solution to both issues is energy-from-waste (EfW) technologies. Many studies have focused on municipal solid waste (MSW) as a potential feedstock, but appear to overlook the potential benefits of commercial and industrial waste (C and IW). In this study, samples of C and IW were collected from three North West waste management companies and Lancaster University campus. The samples were tested for their gross and net calorific value, moisture content, ash content, volatile matter, and also elemental composition to determine their suitability in EfW systems. Intra-sample analysis showed there to be little variation between samples with the exception two samples, from waste management site 3, which showed extensive variation with regards to net calorific value, ash content, and elemental analysis. Comparisons with known fuel types revealed similarities between the sampled C and IW, MSW, and refuse derived fuel (RDF) thereby justifying its potential for use in EfW systems. Mean net calorific value (NCV) was calculated as 9.47 MJ/kg and concentrations of sulphur, nitrogen, and chlorine were found to be below 2%. Potential electrical output was calculated using the NCV of the sampled C and IW coupled with four differing energy generation technologies. Using a conventional incinerator with steam cycle, total electrical output was calculated as 24.9 GWh, based on a plant operating at 100,000 tpa. This value rose to 27.0 GWh when using an integrated gasification combined cycle. A final aspect of this study was to deduce the potential total national electrical output if all suitable C and IW were to be used in EfW systems. Using incineration coupled with a steam turbine, this was determined to be 6 TWh, 1.9% of the national demand thereby contributing 6.5% towards the UK's 2020 renewable electricity target.

29 ENERGY PLANNING, POLICY, AND ECONOMY↗

An LCA model for waste incineration enhanced with new technologies for metal recovery and application to the case of Switzerland

Highlights: • An enhanced process-based LCA model for MSWI is featured and applied in case study. • LCA modeling of recent technological developments for metal recovery from fly ash. • Net release from Swiss MSWI 133 kg CO{sub 2}-eq/tonne waste from attributional LCA perspective. • Net savings from a consequential LCA perspective reach up to 303 kg CO{sub 2}-eq/tonne waste. • Impacts according to ReCiPe and CExD show similar pattern to climate change. - Abstract: A process model of municipal solid waste incinerators (MSWIs) and new technologies for metal recovery from combustion residues was developed. The environmental impact is modeled as a function of waste composition as well as waste treatment and material recovery technologies. The model includes combustion with a grate incinerator, several flue gas treatment technologies, electricity and steam production from waste heat recovery, metal recovery from slag and fly ash, and landfilling of residues and can be tailored to specific plants and sites (software tools can be downloaded free of charge). Application of the model to Switzerland shows that the treatment of one tonne of municipal solid waste results on average in 425 kg CO{sub 2}-eq. generated in the incineration process, and 54 kg CO{sub 2}-eq. accrue in upstream processes such as waste transport and the production of operating materials. Downstream processes, i.e. residue disposal, generates 5 kg CO{sub 2}-eq. Savings from energy recovery are in the range of 67 to 752 kg CO{sub 2}-eq. depending on the assumptions regarding the substituted energy production, while the recovery of metals from slag and fly ash currently results in a net saving of approximately 35 kg CO{sub 2}-eq. A similar impact pattern is observed when assessing the MSWI model for aggregated environmental impacts (ReCiPe) and for non-renewable resource consumption (cumulative exergy demand), except that direct emissions have less and no relevance, respectively, on the total score. The study illustrates that MSWI plants can be an important element of industrial ecology as they provide waste disposal services and can help to close material and energetic cycles.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

Charcoal from anaerobically digested dairy fiber for removal of hydrogen sulfide within biogas

Highlights: • Anaerobically digested (AD) fiber was used for charcoal production via pyrolysis. • Charcoal from AD fiber can effectively adsorb H{sub 2}S from biogas. • Impregnation of charcoal from AD fiber with Na{sub 2}CO{sub 3} increases H{sub 2}S sorption capacity. • Ash in the AD fiber helps the retention of S on the surfaces of the char. • Charcoal manufacture is a promising approach to use abundant AD fiber. - Abstract: Anaerobically digested fibrous solid (AD fiber) is an abundant material that offers potential to produce value-added products such as biochar. The objective of this paper is to better understand how thermochemical processing conditions affect the capacity of biochars derived from AD fiber to adsorb H{sub 2}S from biogas. AD fiber was pyrolyzed in an electric tube reactor at temperatures up to 600 °C and 60 min. The chars were employed for H{sub 2}S scrubbing tests from a synthetic biogas. Results showed that the chars’ capacity for H{sub 2}S removal is comparable to that of activated carbon. An additional step consisting of impregnation of the chars with Na{sub 2}CO{sub 3} resulted in an improved capacity for H{sub 2}S removal. To study the effect of ash, the AD fiber was also subjected to an alternative thermal treatment, hot water extraction (HWE), at 200 °C for 60 min. The resulting HWE material showed no removal of H{sub 2}S from biogas, indicating that the ash and the environment employed for the thermal treatment of AD fiber play an important role in the char’s performance for H{sub 2}S removal. Results also suggest that a portion of the S in the charcoal after the H{sub 2}S sorption process exists as free or adsorbed S (i.e., not chemically bonded to the charcoal).

09 BIOMASS FUELS↗

Extraction Chromatographic Methods in the Sample Preparation Sequence for Thermal Ionization Mass Spectrometric Analysis of Plutonium Isotopes

A sample preparation sequence for actinide isotopic analysis by TIMS is described that includes column-based extraction chromatography as the first separation step, followed by anion exchange column separations. The sequence is designed to include a wet ashing step after the extraction chromatography to prevent any leached extractant or oxalic acid eluent reagents from interfering with subsequent separations, source preparation, or TIMS ionization. TEVA-resin and DGA-resin materials, containing extractants that consist only of C, N, O, and H atoms, were investigated for isolation of plutonium. Radiotracer level studies confirmed expected high yields from column-based separation procedures. Femtogram-level studies were carried out with TIMS detection, using multiple isotopic spikes through the separation sequence. Pu recoveries were 87% and 86% for TEVA- and DGA-resins separations respectively. The Pu recoveries from 400 {mu}L anion-exchange column separations were 89% and 93% for trial sequences incorporating TEVA and DGA-resin. Thus, a prior extraction chromatography step in the sequence did not interfere with the subsequent anion exchange separation when a simple wet ash step was carried out in between these column separations. The average measurement efficiency, for Pu, encompassing the chemical separation recoveries and the TIMS ionization efficiency, was 2.73 {+-} 0.77% (2-sigma) for the DGA-resin trials and 2.67 {+-} 0.54% for the TEVA-resin trials, compared to 3.41% and 2.37% (average 2.89%) for two spikes in the experimental set. These compare with an average measurement efficiency of 2.78 {+-} 1.70%, n = 33 from process benchmark analyses using Pu spikes processed through a sequence of oxalate precipitation, wet ash, iron hydroxide precipitation, and anion exchange column separations. We conclude that extraction chromatography can be a viable separation procedure as part of a multistep sequence for TIMS sample preparation.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Direct Air Capture and Sequestration of CO 2 by Accelerated Indirect Aqueous Mineral Carbonation under Ambient Conditions

Mineralization of gaseous carbon dioxide into solid carbonates using alkaline industrial residues such as coal fly ash has a dual advantage of reducing the carbon dioxide footprint of coal power plants and improving ash utilization. However, the slow mineral carbonation rate under atmospheric conditions is a major challenge, especially when using natural minerals or industrial residues for direct air capture (DAC) of CO 2 . In this study, using coal fly ash samples and concentrated alkali carbonate aqueous solutions as a recyclable solvent, we show the feasibility of coupling mineral carbonation with DAC under atmospheric conditions. Findings show that carbonation efficiency is best under alkaline conditions, achieving as high as ~80% conversion to calcium carbonates within 1 h in a 1.9 M sodium carbonate solution. Based on the experimental results, a process coupling DAC and mineral carbonation that operates entirely under ambient conditions is proposed. Here, the techno-economic and life cycle assessments for the proposed process project a levelized cost of $\$116$–133/t-CO 2 -sequestered (US $\$2019$) and process carbon emissions (GWP) in the range of 0.03–0.25 t-CO 2 e/t-CO 2 -sequestered. Considering the low cost, simplicity, and gigaton-scale sequestration potential, we believe that DAC based on alkaline industrial residue carbonation can be considered a “low-hanging fruit” in the pursuit of negative emissions to combat climate change.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Real Time Volcanic Cloud Products and Predictions for Aviation Alerts

Volcanic eruptions can inject significant amounts of sulfur dioxide (SO2) and volcanic ash into the atmosphere, posing a substantial risk to aviation safety. Ingesting near-real time and Direct Readout satellite volcanic cloud data is vital for improving reliability of volcanic ash forecasts and mitigating the effects of volcanic eruptions on aviation and the economy. NASA volcanic products from the Ozone Monitoring Insrument (OMI) aboard the Aura satellite have been incorporated into Decision Support Systems of many operational agencies. With the Aura mission approaching its 10th anniversary, there is an urgent need to replace OMI data with those from the next generation operational NASA/NOAA Suomi National Polar Partnership (SNPP) satellite. The data provided from these instruments are being incorporated into forecasting models to provide quantitative ash forecasts for air traffic management. This study demonstrates the feasibility of the volcanic near-real time and Direct Readout data products from the new Ozone Monitoring and Profiling Suite (OMPS) ultraviolet sensor onboard SNPP for monitoring and forecasting volcanic clouds. The transition of NASA data production to our operational partners is outlined. Satellite observations are used to constrain volcanic cloud simulations and improve estimates of eruption parameters, resulting in more accurate forecasts. This is demonstrated for the 2012 eruption of Copahue. Volcanic eruptions are modeled using the Goddard Earth Observing System, Version 5 (GEOS-5) and the Goddard Chemistry Aerosol and Radiation Transport (GOCART) model. A hindcast of the disruptive eruption from Iceland's Eyjafjallajokull is used to estimate aviation re-routing costs using Metron Aviation's ATM Tools.

Volcanic ash↗

VIPR III VADR SPIDER Structural Design and Analysis

In support of the National Aeronautics and Space Administration (NASA) Vehicle Integrated Propulsion Research (VIPR) Phase III team to evaluate the volcanic ash environment effects on the Pratt & Whitney F117-PW-100 turbofan engine, NASA Armstrong Flight Research Center has successfully performed structural design and analysis on the Volcanic Ash Distribution Rig (VADR) and the Structural Particulate Integration Device for Engine Research (SPIDER) for the ash ingestion test. Static and dynamic load analyses were performed to ensure no structural failure would occur during the test. Modal analysis was conducted, and the results were used to develop engine power setting avoidance zones. These engine power setting avoidance zones were defined to minimize the dwell time when the natural frequencies of the VADR/SPIDER system coincided with the excitation frequencies of the engine which was operating at various revolutions per minute. Vortex-induced vibration due to engine suction air flow during the ingestion test was also evaluated, but was not a concern.

VADR SPIDER↗

Volcanic Eruption of Cumbre Vieja, La Palma, Spain: A First Insight to the Particulate Matter Injected in the Troposphere

The volcanic eruption of Cumbre Vieja (La Palma Island, Spain), started on 19 September, 2021, and was declared terminated on 25 December, 2021. A complete set of aerosol measurements were deployed around the volcano within the first month of the eruptive activity. This paper describes the results of the observations made at Tazacorte on the west bank of the island where a polarized micro pulse lidar was deployed. The two and a half months analyzed (16 October – 31 December) reveal that the peak height of the lowermost and strongest volcanic plume did not exceed 3 km (mean of 1.43±0.45 km over the whole period) and was highly variable. It steadily increased until week 11 after the eruption start (and 3 weeks before its end) and started decreasing afterwards. The ash mass concentration has been assessed with a method based on the polarization capability of the instrument. Considering the limitation of current remote sensing techniques to detect large to giant particles, the ash mass concentration on one of the days with the highest ash load is estimated to have peaked in the range 800-3200 μg m(exp -3) in the lowermost layer below 2.5 km.

Cumbre Vieja↗

Assessment of Rare Earth Element Fingerprints for Distinguishing Between Site-Related Wastes and Background - 19441

Actinides such as uranium, thorium and radium are known to be present in sites associated with various phases of the cold war weapons research, development and production. Remediation of these sites as well as others associated with chemical plants that may have generated radioactive actinide-containing wastes have been the focus of the Formerly Utilized Sites Remedial Action Program (FUSRAP) for the past 20 years. The goal is to remediate a site to established cleanup standards as efficiently and cost-effectively as possible. For radiologically-contaminated sites, one potential challenge is the presence of non-FUSRAP media such as naturally-occurring radioactive material (NORM) or technologically-enhanced naturally-occurring radioactive material (TENORM), from non-FUSRAP sources, at concentrations exceeding site cleanup standards. Such NORM and TENORM, and even byproduct radionuclides from other unrelated activities on or near the site, can be mistaken for project waste and thus incur significant additional excavation and waste transport and disposal costs. Past studies have provided examples of NORM and non-FUSRAP waste and described strategies to distinguish them from FUSRAP waste. This paper describes various sources of NORM, summarizes the types of project-related waste at some active FUSRAP sites, and identifies TENORM sites from which radionuclides could possibly migrate via various environmental pathways to nearby FUSRAP sites. The authors also examine two Case Studies that calculate distinctive elemental ratios and are examples of tools which may be used for distinguishing FUSRAP waste from other radionuclides present in natural or other man-made contributors to background. Case Study I examines two bodies of data and calculates distinctive elemental ratios between pairs of rare earth elements (REE) to see if significant differences may exist between such ratios in unregulated coal ash residue, common in fill in well-established towns and cities, and FUSRAP waste. The first group of data, consisting of eighteen sample results, was obtained from the FUSRAP Maywood Superfund Site's historical data while the second was obtained from a paper which provided extensive data (more than 100 samples) on the REE content in fly ash residues from three major coal-producing areas in the United States. This example illustrates statistically significant differences in five of six REE ratios and thus provides a potential tool for distinguishing FUSRAP waste from coal ash-based NORM. Case Study II examines differences in the mean REE:Actinide and REE:REE ratios in Welsbach-impacted sample results to distinguish project waste from background. While the purpose of this study was to distinguish project waste from background levels of the radionuclides of concern (ROC), it provides a good example of how one or more ratios could potentially be used to distinguish FUSRAP waste from NORM. Lastly, the authors recommend that future projects ensure robust characterization, that considers all potential radionuclide contributors from both FUSRAP activities as well as from other contributors to background for the region during the Planning Phase of the Data Life Cycle described within the Multi-Agency Radiation Survey and Site Investigation Manual (MARSSIM). It is expected that the incremental characterization sampling and analysis costs will be dwarfed by potential savings from efforts to better delineate and limit remediation to FUSRAP wastes rather than other potentially unregulated contributors to regional background. Other agencies or commercial entities with radiological environmental liabilities similar to FUSRAP would benefit from similar considerations of REEs and other radionuclides that could contribute to regional background. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗