166 research outputs found
RESULTS FOR THE SECOND QUARTER 2010 TANK 50 WAC SLURRY SAMPLE: CHEMICAL AND RADIONUCLIDE CONTAMINANT RESULTS
This report details the chemical and radionuclide contaminant results for the characterization of the 2010 Second Quarter sampling of Tank 50 for the Saltstone Waste Acceptance Criteria (WAC).1 Information from this characterization will be used by Liquid Waste Operations (LWO) to support the transfer of low-level aqueous waste from Tank 50 to the Salt Feed Tank in the Saltstone Facility in Z-Area, where the waste will be immobilized. This information is also used to update the Tank 50 Waste Characterization System. The following conclusions are drawn from the analytical results provided in this report: (1) The concentrations of the reported chemical and radioactive contaminants were less than their respective WAC targets or limits unless noted in this section. (2) The reported detection limits for {sup 94}Nb and {sup 144}Ce are above both the established and requested limits from References 4 and 6. (3) The reported detection limits for {sup 247}Cm and {sup 249}Cf are above the requested limits from Reference 4. However, they are below the limits established in Reference 6. (4) The reported detection limit for Isopar L is greater than the limit from Table 3 of the WAC. (5) A measurable concentration of Norpar 13 is present in the sample. The reported concentration is greater than the requested limit from Table 4 and Attachment 8.2 of the WAC. (6) Isopar L and Norpar 13 have limited solubility in aqueous solutions making it difficult to obtain consistent and reliable sub-samples. The values reported in this memo are the concentrations in the sub-sample as detected by the GC/MS; however, the results may not accurately represent the concentrations of the analytes in Tank 50. (7) The detection limit for isopropanol has been lowered from 0.5 mg/L to 0.25 mg/L{sup 7}. This revised limit now satisfies the limit in Table 4 of the WAC
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RESULTS FOR THE SECOND QUARTER 2009 TANK 50 WAC SLURRY SAMPLE CHEMICAL CONTAMINANT RESULTS
Navigating Liminal Legalities Along Pathways To Citizenship: Immigrant Vulnerability and the Role of Mediating Institutions
In this report, we summarize the findings of research funded by the Russell Sage Foundation and conducted in Southern California over the course of eighteen months between January 2014 and September 2015. This time period coincided with the announcement of and subsequent legal challenges to the DACA and DAPA program – a period characterized by extreme legal uncertainty over the availability and scope of these “Executive Relief” programs. Drawing from 16 in-depth interviews with staff of 10 different immigrant serving organizations and 47 interviews with noncitizens in the Los Angeles and Orange County areas, we captured the on-the-ground challenges facing noncitizens and community based organizations as the scope and availability of Executive Relief was debated. In our research, we focused on the hardships and barriers to incorporation imposed by liminal legal status, the challenges faced by organizations mediating between their constituents and the state in periods of legal uncertainty, and the ways that uncertainty has reshaped the social, political and legal environment in which immigrant-serving organizations and their constituents interact. Our research is ongoing, but here we offer our preliminary findings for some of our research questions
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Extension of Studies with 3M Empore TM and Selentec MAG *SEP SM Technologies for Improved Radionuclide Field Sampling
The Savannah River Technology Center is evaluating new field sampling methodologies to more easily determine concentrations of radionuclides in aqueous systems. One methodology studied makes use of 3M EmporeTM disks. The disks are composed of selective resins embedded in a Teflon support. The disks remove the ion of interest from aqueous solutions when the solution is passed through the disk. The disk can then be counted directly to quantify the isotope of interest. Four types of disks were studied during this work: for the extraction of technetium (two types), cesium, plutonium, and strontium. A sampler has been developed for automated, unattended, in situ use of the EmporeTM disks
Impact of Irradiation on Solvent used in SRS Waste Treatment Processes -9122
ABSTRACT Savannah River Site (SRS) will use a Caustic Side Solvent Extraction (CSSX) process to selectively remove radioactive Cs-137 from the caustic High Level Waste (HLW) salt solutions stored in the large carbon steel waste tanks in the SRS Tank Farm. This HLW resulted from several decades of operations at SRS to produce nuclear materials for the United States Government. The removed Cs-137 will be sent to the Defense Waste Processing Facility (DWPF) where it will be immobilized along with the HLW sludges from the SRS Tank Farm into a borosilicate glass that will be put into permanent disposal. Currently the CSSX process is operating on an interim basis in the Modular Caustic Side Solvent Extraction Unit (MCU) facility. Eventually the process will occur in the full scale Salt Waste Processing Facility (SWPF) currently being built. The organic solvent developed for the process is primarily a mixture of the Isopar ® L (a blend of C 10 -C 12 branched alkanes such as dodecane) and an alkyl aryl polyether added as a Modifier (commonly called Cs-7SB) to enhance the solubility of the extractant which is a calixarene-crown ether. The solvent also includes trioctylamine to mitigate the adverse impact of lipophilic agents on the stripping of the cesium into nitric acid. Since the mixture is primarily organic hydrocarbons, it is expected that radiolysis of the mixture with gamma rays and beta particles from the Cs-137 will produce the flammable gas H 2 and also eventually degrade the solvent. For example, much research has been performed on the radiolysis of the organic solvent used in the tributylphosphate (TPB) extraction process (PUREX process) that has been used at SRS and in many other countries for several decades to separate U and Pu from radioactive U-235 fission products such as Cs-137. [1] The purpose of this study was to investigate the radiolysis of the organic solvent for the CSSX process. Researchers at Savannah River National Laboratory (SRNL) irradiated samples of solvent with Co-60 gamma rays. Prior to the irradiation, the solvent was contacted with the aqueous solutions that will be used in the MCU and SWPF facilities. These were the aqueous caustic salt feed, the scrub solution, and wash water. The rates of radiolytic H 2 production were measured both by determining the composition of the gases produced and by measuring pressures produced during radiolysis. The irradiated solvents were then analyzed by various analytical techniques to assess how much of the Isopar ® L, the Modifier, and the extractant had decomposed
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Radionuclide analysis using solid phase extraction disks
The use of solid phase extraction disks was studied for the quantification of selected radionuclides in aqueous solutions. The extraction of four radionuclides using six types (two commercial, four test materials) of 3M Empore{trademark} RAD disks was studied. The radionuclides studied were: technetium-99 (two types of disks), cesium-137 (two types), strontium-90 (one type), plutonium-238 (one type). Extractions were tested from DI water, river water and seawater. Extraction efficiency, kinetics (flow rate past the disk), capacity, and potential interferences were studied as well as quantification methods
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Performance of a Buried Radioactive High Level Waste Glass After 24 Years
A radioactive high level waste glass was made in 1980 with Savannah River Site (SRS) Tank 15 waste. This glass was buried in the SRS burial ground for 24 years but lysimeter data was only available for the first 8 years. The glass was exhumed and analyzed in 2004. The glass was predicted to be very durable and laboratory tests confirmed the durability response. The laboratory results indicated that the glass was very durable as did analysis of the lysimeter data. Scanning electron microscopy of the glass burial surface showed no significant glass alteration consistent with the results of the laboratory and field tests. No detectable Pu, Am, Cm, Np, or Ru leached from the glass into the surrounding sediment. Leaching of {beta}/{delta} from {sup 90}Sr and {sup 137}Cs in the glass was diffusion controlled. Less than 0.5% of the Cs and Sr in the glass leached into the surrounding sediment, with >99% of the leached radionuclides remaining within 8 centimeters of the glass pellet
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Development of Alternative Glass Formulations for Vitrification of Excess Plutonium - SEM/XRD Analyses
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