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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 397 records · Page 22
All sourcesNASA NTRSDOE OSTI
DOE OSTI2014

Coupled slow and fast surface dynamics in an electrocatalytic oscillator: Model and simulations

The co-existence of disparate time scales is pervasive in many systems. In particular for surface reactions, it has been shown that the long-term evolution of the core oscillator is decisively influenced by slow surface changes, such as progressing deactivation. Here we present an in-depth numerical investigation of the coupled slow and fast surface dynamics in an electrocatalytic oscillator. The model consists of four nonlinear coupled ordinary differential equations, investigated over a wide parameter range. Besides the conventional bifurcation analysis, the system was studied by means of high-resolution period and Lyapunov diagrams. It was observed that the bifurcation diagram changes considerably as the irreversible surface poisoning evolves, and the oscillatory region shrinks. The qualitative dynamics changes accordingly and the chaotic oscillations are dramatically suppressed. Nevertheless, periodic cascades are preserved in a confined region of the resistance vs. voltage diagram. Numerical results are compared to experiments published earlier and the latter reinterpreted. Finally, the comprehensive description of the time-evolution in the period and Lyapunov diagrams suggests further experimental studies correlating the evolution of the system's dynamics with changes of the catalyst structure.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2014

Cascade energy transfer versus charge separation in ladder-type oligo(p-phenylene)/ZnO hybrid structures for light-emitting applications

Usability of inorganic/organic semiconductor hybrid structures for light-emitting applications can be intrinsically limited by an unfavorable interfacial energy level alignment causing charge separation and nonradiative deactivation. Introducing cascaded energy transfer funneling away the excitation energy from the interface by transfer to a secondary acceptor molecule enables us to overcome this issue. We demonstrate a substantial recovery of the light output along with high inorganic-to-organic exciton conversion rates up to room temperature.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
DOE OSTI2015

Lattice distortion mechanism study of TiO{sub 2} nanoparticles during photocatalysis degradation and reactivation

In this paper, the photocatalytic process of TiO{sub 2} (P25) is directly characterized by using a positron annihilation lifetime spectroscopy (PALS), high-resolution transmission electron microscopy (HRTEM), Photoluminescence spectroscopy (PL) and UV Raman spectroscopy (Raman). The experimental results reveal that: 1) From PALS measurements, because τ{sub 1} and τ{sub 2} values and their intensity (I{sub 1} and I{sub 2}) assigned to the different size and amounts of defects, respectively, their variations indicate the formation of different types and amounts of defects during the absorption and degradation. 2) HRTEM observations show that the lattice images become partly blurring when the methylene blue is fully degradated, and clear again after exposed in the air for 30 days. According to the results, we propose a mechanism that the lattice distortion induces the defects as electron capture sites and provides energy for improving photocatalytic process. Meanwhile, the lattice distortion relaxation after exposing in the air for 30 days perfectly explains the gradual deactivation of TiO{sub 2}, because the smaller vacancy defects grow and agglomerate through the several photocatalytic processes. The instrumental PL and Raman are also used to analyze the samples and approved the results of PALS and HRTEM.

36 MATERIALS SCIENCE↗
DOE OSTI2015

The geometrical change and intramolecular energy transfer upon S{sub 1}←S{sub 0} excitation in cyclopentanone

The ultrafast dynamics in vibrationally hot S{sub 1} electronic excited state in cyclopentanone molecule was discovered with time resolved spectroscopy. Investigation of the geometry change upon the S{sub 1}←S{sub 0} excitation and D{sub 0}←S{sub 1} ionization has shown that the dihedral angle between the C=O bond and the plane given by the carbonyl and the α-carbons is 180° either in S{sub 0} or D{sub 0} state and is reduced to 145.8° by out-out-plane deformation of the oxygen in S{sub 1} state according to the theoretical calculation. The time domain experiments with femtosecond resolution have given rich insights into the energy transfer of the cyclopentanone molecule. The molecules are excited to the vibrationally hot S{sub 1} (n, π{sup ∗}) state following absorption of one 267-nm photon. It is found that the population of the S{sub 1} (n, π{sup ∗}) state undergoes ultrafast internal conversion to the highly vibrationally hot S{sub 0} state within 80 fs and nonradiative deactivation by intersystem crossing to triplet T{sub 1} (n, π{sup *}) state occurring in 3.14 ps. Several Rydberg states have worked as stepping stones during the ionization. The available energy was distributed in the symmetric methylene group wagging and the symmetric skeletal ring breathing modes in D{sub 0} state.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2018

Erratum to: “The Fluorescence and Electronic Structure of Phenyl-Substituted Tetraazachlorin Molecules” [Optics and Spectroscopy 117, 722 (2014)]

should read “porphyrazine” instead of “porphyrazin”;should read “intersystem crossing” instead of “intercombinational conversion”;should read “mirror-symmetrical” instead of “reflection-symmetric”;should read “fluorescence enhancement” instead of “fluorescence buildup.”Page 722, Abstract, lines 9–10 from the top, the sentence should read:This characteristic increases upon tetrapyrrole phenylation.Page 727, left column, lines 17–18 from the top, the sentence should read:The vibronic transition parts of the emission spectrum are diffuse, (…)Page 727, left column, lines 29–30 from the top, the sentence should read:Note that the Stokes shift in these cases is relatively large.Page 729, left column, lines 8–10 from the bottom, the sentence should read:For H{sub 2}Ph{sub 8}TAC{sup mp} and H{sub 2}Ph{sub 6}TAC{sup tm}, the enhancement of fluorescence is weaker than in the former case: on cooling, τ{sub F} is increased by a factor of 4–5 in MTHF and by a factor of only 2.6–3 in toluene.Page 729, right column, lines 9–10 from the footnote, the sentence should read:It is seen from Table 1 that our results agree reasonably well with previously reported data.Page 730, left column, lines 16–19 from the top, the sentence should read:The lifetime for the outgassed H{sub 2}TAP solution intoluene (τ{sub T}{sup 0}) was measured by A.S. Stasheuski as phosphorescence decay at λ{sub reg} = 1070 nm using the setup described in [29].Page 730, left column, lines 20–23 from the top, the sentence should read:The τ{sub T} value derived from the kinetics of the rise of singlet oxygen luminescence [26] for the nonoutgassed solution at λ{sub reg} = 1272 nm is 162 ns;Page 730, right column, lines 25–27 from the top, the sentence should read:Therefore, for H{sub 2}TAP (λ{sub F}{sup 00}≈ 620 nm), the internal conversion probability should not be high.Page 731, left column, the heading of Table 2 should read:Bond lengths in the porphine macrocycle (Å).Page 731, left column, lines 3–6 from the top, the sentence should read:For elucidating the mechanism of the deactivation of the S{sub 1} state, it was of essential interest to see whether the enhancement of H{sub 2}TAP fluorescence would be observed at 77 K.Page 733, left column, lines 2–3 from the top, the sentence should read:The corresponding difference for the H{sub 2}P–H{sub 2}C pair is 0.013 Å.Page 733, left column, lines 14–16 from the top, the sentence should read:The macrocycle undergoes additional contraction, and the symmetry of its conjugated system is very close to D{sub 2h}.Page 733, right column, line 21 from the top should read:Replacement of the methine bridges (…)Page 734, left column, lines 8–11 from the figure caption, the sentence should read:This is the main reason of the large bathochromic shift of the Soret band of H{sub 2}Ph{sub 8}TAP and MgPh{sub 8}TAP [16] relative to H{sub 2}TAP and MgTAP, respectively.Page 734, left column, lines 1–4 from the bottom, the sentence should read:The complete INDO/Sm calculation yields the corresponding quantitative characteristics, which are in good agreement with experimental data (see below).Page 740, left column, reference no. 25 should read:25. V. A. Galievsky, A. S. Stasheuski, V. V. Kiselyov, A. I. Shabusov, M. V. Belkov, and B. M. Dzhagarov, Instrum. Exp. Tech. 53, 568 (2010).25. V. A. Galievsky, A. S. Stasheuski, V. V. Kiselyov, A. I. Shabusov, M. V. Belkov, and B. M. Dzhagarov, Instrum. Exp. Tech. 53, 568 (2010).30. V. L. Ermolaev and E. B. Sveshnikova, Acta Phys. Pol. 34, 771 (1968).

74 ATOMIC AND MOLECULAR PHYSICS↗
DOE OSTI2020

Recent Progress to Understand and Improve Zeolite Stability in the Aqueous Medium

The work reviewed here attempts to summarize the growing literature on zeolite stability in hot liquid water. This required to first establish the nature, structure and interactions of the active sites in Brønsted and Lewis acidic microporous materials in the presence of liquid water. This understanding was then transferred to zeolite stability and catalyst deactivation. While early results correctly established Si–O–Si hydrolysis as the dominant pathway compared to the Si–O–Al hydrolysis observed in steaming, it also focused extensively on the positive role of framework and extra-framework Al in stabilizing zeolites. However, stability was instead found to more directly correlate with the number of internal structural defects and intraporous water concentration. Stabilization protocols for Brønsted acidic zeolites are described in detail. In the case of Lewis acidic zeolites, their inherent hydrophobic behavior (Si/M >100) makes them more resistant towards water, however, issues such as reversible carbonaceous species formation as well as irreversible metal leaching and fouling remain. Finally, we summarize the most important factors in designing robust and efficient zeolite catalysts made to withstand hot liquid water.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2017

Innovative approach to reduction of waste streams for cutting operations in remote environments

SRNL proposes to develop and demonstrate an approach using the SRNL rotary microfilter (RMF) technology for reducing waste streams in remote cutting operations during decontamination operations. SRNL offers to collaborate with Tokyo Electric Power Company (TEPCO) in evaluation, testing, and utilization of SRNL’s radiation-hardened rotary microfilter in the deactivation and decommissioning (D&D) operations of the Fukushima Daiichi Nuclear Power Station (NPS). Refinement of the scope and associated costs will be conducted in consultation with TEPCO.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗
DOE OSTI2020

FIU Project 3: Waste and D&D Engineering and Technology Development [Slides]

This project focuses on delivering solutions under deactivation and decommissioning (D&D) in support of DOE EM-4.11 as well as IT development for environmental applications (KM-IT for EM-4.11) and waste & material management (WIMS for EM-4.22). All technology development related activities will also engage the Office of Technology Development (EM-3.2). This work is also relevant to infrastructure management activities being carried out at DOE sites such as Oak Ridge, Savannah River, Hanford, Idaho and Portsmouth. As appropriate and within the parameters of the DOE-FIU Cooperative Agreement (CA), coordination at the proper level will occur with the sites and national laboratories involved in the project research efforts as well as with the points-of-contact at DOE HQ (e.g., HQ Project Leads, HQ Field Liaisons, Office of Technology Development, CA Technical Monitor, COR, etc.).

96 KNOWLEDGE MANAGEMENT AND PRESERVATION↗
DOE OSTI2021

Depowering of Batteries to Reduce Cost of Ownership

(1) Executive Summary: End of life batteries (EOLBs) present a cost and safety liability for their owners and stakeholders. This is due flammability, energy, and power with EOLBs. Current approaches include cumbersome, expensive packaging, specialized shipping, regulated storage, and they are responsible for over half of the cost of recycling. They all expensively and inadequately address symptoms. OnTo has developed and proven a simple way to resolve the problem systemically, through depowering of lithium-ion batteries (and most any battery other than lead). The low-cost process removes flammability, power, and energy in EOLBs through non-toxic chemical processing. The opportunity for commerce of inert scrap is at least $5 billion greater than the commerce in hazardous scrap, all made possible through OnTo’s technology for efficiency and safety. (2) Depowering Improves Safety and Decreases Cost of Battery Ownership: OnTo’s depowering technology will remove half of the cost of EOLB management and recycling. Without this technology, EOLB recycling will always be a liability. EOLB is hazardous due to inherent flammability of electrolyte and lithium. The shipping and commerce of EOLBs is costly and dangerous all along the chain of custody from owner, dealership/shop, shipper, second-life sorter, (shipper again), and finally to the destination facility recycler. OnTo’s depowering service renders inert most any EOLB packs, modules, and cells. The technology uses a brief, non-toxic treatment applicable to most any chemistry. The industry needs a safe, simple, modular, and inexpensive method to render EOLBs as inert scrap. OnTo’s deactivation system is scalable to the needs of any customer along the EOLB chain of custody. (3) Evidence of Successful Depowering: Untreated batteries will catch fire and explode under abuse conditions such as heat or crush. Slide 2 below shows that untreated batteries will blow-up and expel their internal components with heating, after OnTo’s depowering treatment, the same battery is inert with the same heat treatment (Fig. 7 in the slide). Depowering also removes electrolyte reactivity, eliminating the production of HF and other toxins (Fig 6. in the slide) The depowering process is applicable to large, 26 Ah cells. Fig. 5 in the slide shows the removal of all the electrolyte from whole cells. Removal of flammable material from an EOLB contributes to the inert behavior. OnTo developed this technology through a project supported by the US Department of Energy EERE program, with partners including Seattle King County Metro Transit. While OnTo has generated evidence of successful depowering of batteries, in 2020, a follow-on voucher opportunity for third party analysis of depowered cells and materials was approved through CalTestBed. The expertise of the battery and materials research groups at Lawrence Berkeley National Laboratory will characterize these depowered cells to provide better understanding of the materials level changes in depowering. (4) Pilot Plant for Depowering EOLBs: Making the spoke work in hub-and-spoke While other companies are marketing the hub-and-spoke approach for recycling EOLBs, they rely on dangerous, expensive shredding methods with flimsy IP protection. OnTo offers the only patented, proven ability to depower EOLBs from most any chemistry – at half of the capital cost required for shredding, while eliminating the liability, danger, and waste streams inherent with shredding. The proposed commercial pilot facility is (5) OnTo Technology LLC Company: OnTo develops advanced battery recycling innovations that produce manufacturing quality electrode materials from recycled batteries. Their patented Cathode-healing™ and Deactivation/Depowering processes improve safety and reduce the cost of recycling. OnTo’s breakthrough technologies produce advanced materials for manufacturing batteries useful in applications from portable power to electric vehicles. Contact: Steve Sloop OnTo Technology LLC, 63221 Service Road, STE F, Bend, OR 97703, ssloop@onto-technology.com , 541-389-7897

deactivation↗
DOE OSTI2021

Li-ion Identification For the Next Generation of Cathode Recycling

OnTo’s end-to-end solution will demonstrate (in partnership/collaboration with relevant industries) collection of lithium-ion batteries through recycling of cathode material. The DISCC project will prototype 1) deactivation of batteries 2) identification 3) sorting using automated techniques, 4) cutting with waterjet technology and 5) Cathode-Healing™ to produce valuable cathodes from scrap batteries.

25 ENERGY STORAGE↗
DOE OSTI2023

Radiation Hardened Foam Cold Test Plan - Phase II: Foam Characterization Testing and Environmental Chamber Testing of FoamBag Fixative Foam

This document outlines the Phase II test objectives and implementation plan for a down-select foam fixative technology intended to facilitate activities in support of the Savannah River Site (SRS) F/H labs deactivation and decommissioning (D&D) efforts. It is a collaborative effort between Savannah River National Laboratory (SRNL), Florida International University (FIU), and the SRS F/H labs team intended to test and evaluate the potential of a polyurethane resin foam in mitigating the release of contamination during dismantling operations on radioactively contaminated piping in legacy facilities. The cold test plan addresses specific requirements highlighted by site and safety personnel and will be executed at FIU and SRNL test and lab facilities. Results from the cold tests will inform the hot test at F/H labs, which will use the foam fixative to confine and/or isolate residual contamination within a 3-dimensional void space of Hastelloy C-22 piping designated for removal from the area and transported to a designated disposal facility. Phase I testing was previously conducted using Hilti CP620 fixative foam. Results from Phase I testing indicate Hilti CP-620 fixative foam is incompatible with SRS site hot taps as an effective foam delivery method into Hastelloy C-22 piping. Phase II testing will be conducted using FoamBag TM fixative foam as an alternative fixative foam option. Phase II testing will address eight test objectives: (1) evaluation of the adhesion and bonding properties of FoamBag TM in Hastelloy C-22 piping, (2) evaluation of the adhesion of FoamBag TM in piping under various moisture conditions, (3) determination of the heat profile of FoamBag TM during curing, (4) determination of the internal pipe pressure after FoamBag TM deployment and curing, (5) conduct a leak test to determine if FoamBag TM is effective at creating a full seal within piping, (6) headspace testing of FoamBag TM to determine if there are any associated off-gas hazards during FoamBag TM curing, (7) conduct environmental chamber testing of FoamBag TM to understand how environmental parameters impacts FoamBag TM curing, and (8) conduct fire testing to evaluate FoamBag TM fire retardant characteristics.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗
DOE OSTI2024

Identifying Controlling Variables for Mercury Vapors in Alpha-4 at Y-12: Two Year Data Collection Update

Multiple sensor packages were deployed at Alpha-4 by SRNL, in collaboration with United Cleanup Oak Ridge LLC (UCOR), to monitor mercury vapor concentrations and meteorological parameters. These sensors collected data, inside and outside of the legacy-use facility, for approximately two years. Though data gaps still exist, particularly in colder months, several controlling variables were identified that govern mercury vapor concentrations within Alpha-4. Temperature, barometric pressure gradients, humidity, and wind speed have been identified as controlling variables. A strong positive correlation was seen between mercury vapor concentrations and temperature which generally followed diurnal fluctuations. Temperatures below approximately 10 degrees Celsius did not show any spikes above the PEL, indicating more work can be performed at any time during the winter months – more data should be collected to confirm consistency in this finding. Additionally, spikes in mercury vapor concentrations above that of the permissible exposure limit (PEL; 100 µg/m 3 ) occurred primarily in late afternoon or evening/overnight hours (between 3 PM and 6 AM), which suggests D&D operations might be best scheduled during morning or daytime hours prior to the late afternoon. However, a limited number of spikes did occur outside of the identified window, although this may be attributed to disturbances in air flow and mercury vapor release from work activities performed inside of the Alpha-4 building. The analysis conducted allows for a strong predictive capability for estimating mercury vapor concentrations based upon accurate meteorological parameters. Still, additional data collection, particularly in the winter months, could help to strengthen the predictive power and validate the identified data trends. Further, increased temporal resolution could also help to better characterize the incipient stages of the increases and decreases in the mercury vapor concentration. Continued monitoring support by SRNL at Y-12 is underway at Alpha-4 to further close remaining data gaps and support deactivation and decommissioning work. Within a collaborative effort with UCOR, the SRNL team is collecting mercury vapor data to study the efficacy of a novel mercury suppressant, FerroBlack® which was recently deployed at Alpha-4. In addition, modifications to the current monitoring setup to increase measurement resolution is also being investigated.

54 ENVIRONMENTAL SCIENCES↗
NASA NTRS2005

Polar processing and development of the 2004 Antarctic ozone hole : first results from MLS on Aura

The Microwave Limb Sounder (MLS) on Aura is providing an extensive data set on stratospheric winter polar processing, including the first daily global observations of HCl, together with simultaneous measurements of ClO, HNO3, H2O, O3, N2O, and temperature (among others). We present first results charting the evolution of these quantities during the 2004 Antarctic late winter. MLS observations of chlorine deactivation and ozone loss during this period are shown to be consistent with results from the SLIMCAT chemical transport model.

Microwave Limb Sounder (MLS)↗
DOE OSTI2019

Active lithium analysis for the elimination of battery thermal runaway

Active lithium that is still present in end-of-life batteries poses threats of flammability and reactivity, making disposal and transportation unsafe and costly. OnTo’s deactivation method uses supercritical CO2 to eliminate the hazards of active lithium. Until now, there has been no quantitative method to determine the active lithium content within a battery. The objective of this project is to demonstrate a simple, rapid measurement of active lithium to evaluate battery treatment processes and eliminate class 9 hazards.

battery safety↗
DOE OSTI2015

Hanford site asbestos management lessons learned - 15183

The U.S. Department of Energy (DOE) is responsible for the environmental cleanup of the Hanford Site central plateau. As part of this responsibility, DOE contractors conduct deactivation, decommissioning, decontamination, and demolition (D4) of retired/inactive facilities, including very large chemical processing facilities. To date, DOE contractors have demolished hundreds of facilities, reducing baseline site maintenance costs and reducing the environmental threats and hazards that the degrading buildings present. Many of these Hanford facilities include asbestos-containing materials (as well as other hazardous components), which must be managed in compliance with applicable regulations and standards. In most cases, the facilities are demolished as Comprehensive Environmental Response, Compensation and Liability Act (CERCLA) removal or remedial actions. In an effort to streamline cleanup operations and to utilize site cleanup funding more efficiently, while still being protective of personnel and the environment, agreements were reached between the US Environmental Protection Agency (EPA) Hanford Project Office, the Washington Department of Ecology (Ecology), the Benton Clean Air Agency (BCAA) and the US Department of Energy Richland Operations Office (DOE-RL) on approaches to be utilized for demolition. One of these approaches would involve leaving cement asbestos board siding (e.g. transite), an EPA National Emissions Standards for Hazardous Air Pollutants (NESHAP) Category II non-friable asbestos-containing material, in place during demolition using heavy equipment, employing a set of controls that would maintain protection of personnel and the environment. This agreement was documented in a number of formal communications, including Notices of Intent issued as required by the asbestos NESHAP regulation, letters between the various agencies, CERCLA work plans, and the approved contractor baselines. A large number of buildings were demolished with transite siding in place, using the agreed upon controls and approaches. Personnel breathing zone and work area perimeter monitoring verified that the controls employed were protective in that there were no exceedances of permissible exposure limits during or after the demolition operations. EPA later reconsidered their previous concurrence with demolishing transite materials in place and issued a joint letter with Ecology revoking concurrence on any of the aforementioned CERCLA decision documents and associated work plans. DOE and their contractors took action to comply with the approach to demolition preferred by EPA for future demolitions, and initiated a series of actions to modify asbestos management practices in their operations accordingly. This paper will discuss both the actions taken to address EPA concerns with sites where transite materials were left in place for demolition and actions taken to ensure that the central plateau D4 program complies with the 40 CFR 61 Subpart M, National Emission Standard for Asbestos, (Asbestos NESHAP) methods for asbestos management. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗
DOE OSTI2015

Characterization of a contaminated facility and associated soils in support of D and D and subsequent soil remediation - 15292

Before starting any D and D field work at a United States Department of Energy (DOE) facility such as the Savannah River Site (SRS), it is recommended that a complete review and understanding of the full nature and extent of any contamination located in or previously associated with that facility is known. An integral aspect of this review and research entails a complete characterization of that facility, including, but not limited to, Toxic Substances Control Act (TSCA) limits for Polychlorinated Biphenyl (PCB), radiological, Resource Conservation and Recovery Act of 1976 (RCRA) and other hazardous chemicals, etc. A thorough characterization of a facility and its underlying soils supports: - establishment of safe working conditions to protect human health and environment - Deactivation and Decommissioning (D and D) methodology - cost estimates to support future budget planning for D and D and soil cleanup A prime example of this is documented in the characterization of the 690-N, Process Heat Exchanger Repair Facility that had a history of PCB and radioactive contamination. Characterization of 690-N included the sampling and analysis of concrete and underlying soils for radiological, PCB and hazardous contaminants. In addition, a sump, the walls of the facility, expansion joint material and the metal base of a drill press were characterized. Results of this comprehensive characterization of the 690-N Building are provided in a detailed report. Analytical results indicate minimal radiological, PCB, or RCRA hazardous contamination is present in the concrete floor slab (industrial exposure levels) and on the steel hut walls. Soils below the concrete floor slab show only trace amounts of radiological contamination and are well below TSCA and RCRA limits. Subsequent decommissioning/demolition activities can be performed safely without harming people or the environment, and cost estimates to perform building demolition can be developed for future budget planning. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗
DOE OSTI2015

Case study in corporate memory recovery: Hanford tank farms miscellaneous underground waste storage tanks - 15344

In addition to managing the 177 underground waste storage tanks containing 212,000 m{sup 3} (56 million gal) of radioactive waste at the U. S. Department of Energy's Hanford Site 200 Area Tank Farms, Washington River Protection Solutions LLC is responsible for managing numerous small catch tanks and special surveillance facilities. These are collectively known as 'MUSTs' - Miscellaneous Underground Storage Tanks. The MUSTs typically collected drainage and flushes during waste transfer system piping changes; special surveillance facilities supported Tank Farm processes including post-World War II uranium recovery and later fission product recovery from tank wastes. Most were removed from service following deactivation of the single-shell tank system in 1980 and stabilized by pumping the remaining liquids from them. The MUSTs were isolated by blanking connecting transfer lines and adding weatherproofing to prevent rainwater entry. Over the next 30 years MUST operating records were dispersed into large electronic databases or transferred to the National Archives Regional Center in Seattle, Washington. During 2014 an effort to re-acquire the historical bases for the MUSTs' published waste volumes was undertaken. Corporate Memory Recovery from a variety of record sources allowed waste volumes to be initially determined for 21 MUSTs, and waste volumes to be adjusted for 37 others. Precursors and symptoms of Corporate Memory Loss were identified in the context of MUST records recovery. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗
DOE OSTI2015

Management of technetium contaminated demolition debris from the gaseous diffusion plants at the east Tennessee Technology Park - 15422

The demolition of the final section of the gaseous diffusion plant (GDP) facility formerly known as K-25 at the East Tennessee Technology Park was completed in December of 2013, with the final shipment of waste completed only six months later in June 2014. While most of the radioactive waste shipments would be considered 'routine' by today's standards (lower activity waste was disposed onsite at the Environmental Management Waste Management Facility [EMWMF] and at some offsite commercial disposal facilities with higher activity waste making its way across country to the Nevada National Security Site [NNSS] disposal facility) the final section of K-25, consisting of six cascade 'units', presented some unique technical and stakeholder challenges. Portions of this final section of K-25 were presumed to be heavily contaminated with Technetium-99 (Tc-99) based on sampling and analysis activities conducted during facility deactivation. Tc-99 is known to be highly mobile under a variety of environmental conditions, and is suspected to be potentially mobile in unmitigated landfill conditions, resulting in the need to implement additional engineered controls during facility demolition as well as throughout the management of the resultant waste. A variety of controls were implemented to ensure Tc-99 mobility was controlled and possible consequences mitigated, including isolation and offsite shipment of highest Tc-99 concentration components, as well as construction of a 'cell within a cell' at the EMWMF. This paper will examine the process utilized to develop the controls for management of Tc-99 contaminated waste and will describe those controls. Additionally, it will describe the stakeholder involvement and approval process as well as examining and documenting the efficacy of the controls that were implemented. Finally, this paper will discuss lessons learned from this first of a kind demolition effort and how this experience can be utilized to further refine the Tc-99 waste management approach for the remaining GDPs at ETTP. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗