Sample records for non-acid elution nae

  1. EVALUATION OF POTENTIAL ELUANTS FOR NON-ACID ELUTION OF CESIUM FROM RESORCINOL-FORMALDEHYDE RESIN

    SciTech Connect (OSTI)

    Adu-Wusu, K.; Pennebaker, F.

    2010-12-22T23:59:59.000Z

    Small-column ion exchange (SCIX) units installed in high-level waste tanks to remove Cs-137 from highly alkaline salt solutions are among the waste treatment plans in the DOE-complex. Spherical Resorcinol-Formaldehyde (sRF) is the ion exchange resin selected for use in the Hanford Waste Treatment and Immobilization Plant (WTP). It is also the primary ion exchange material under consideration for SCIX at the Hanford site. The elution step of the multi-step ion exchange process is typically done with 0.5 M nitric acid. An acid eluant is a potential hazard in the event of a spill, leak, etc. because the high-level waste tanks are made of carbon steel. Corrosion and associated structural damage may ensue. A study has been conducted to explore non-acid elution as an alternative. Batch contact sorption equilibrium screening tests have been conducted with 36 potential non-acid eluants. The sorption tests involve equilibrating each cesium-containing eluant solution with the sRF resin for 48 hours at 25 C in a shaker oven. In the sorption tests, an eluant is deemed to have a high cesium elution potential if it minimizes cesium sorption onto the sRF resin. The top candidates (based on lowest cesium sorption distribution coefficients) include ammonium carbonate, ammonium carbonate/ammonium hydroxide, ammonium bicarbonate, rubidium carbonate, ammonium acetate, ammonium acetate/ammonium hydroxide, ammonium bicarbonate/ammonium hydroxide, calcium chloride, and magnesium chloride. A select few of the top candidate eluants from the screening tests were subjected to actual sorption (loading) and elution tests to confirm their elution ability. The actual sorption (loading) and elution tests mimicked the typical sRF-cesium ion exchange process (i.e., sorption or loading, caustic wash, water rinse, and elution) via batch contact sorption and quasi column caustic wash/water rinse/elution. The eluants tested included ammonium carbonate, ammonium acetate, calcium acetate, magnesium acetate, and nitric acid. Calcium acetate and magnesium acetate were substitutes for calcium chloride and magnesium chloride respectively due to corrosion concerns. Nitric acid was selected for benchmarking since it is the baseline cesium eluant for sRF resin. The cesium elution performance of ammonium carbonate and ammonium acetate was approximately the same as the benchmark eluant, nitric acid. Ninety-seven (97), 94, and 100% percent of the cesium sorbed or loaded were eluted by ammonium carbonate, ammonium acetate, and nitric acid was respectively. The performance of calcium acetate and magnesium acetate, on the other hand, was mediocre. Percent elution was 16 and 8 respectively.

  2. EVALUATION OF POTENTIAL ELUANTS FOR NON-ACID ELUTION OF CESIUM FROM SPHERICAL RESORCINOL-FORMALDEHYDE RESIN

    SciTech Connect (OSTI)

    Adu-Wusu, K.; Nash, C.; Pennebaker, F.

    2011-10-23T23:59:59.000Z

    Ion Exchange column loading and elution of cesium from spherical resorcinol-formaldehyde resin have been conducted for two potential non-acid eluants -(NH{sub 4}){sub 2}CO{sub 3} and CH{sub 3}COONH{sub 4}. The results revealed encouraging cesium elution performance. 100% elution was achieved in at most 22 hours ({approx}28 bed volumes) of elution. Elution performance was fairly high at 6 hours ({approx}8 bed volumes) of elution for some of the eluants and also practically comparable to the benchmark acid eluant (HNO{sub 3}). Hence, it is quite possible 100% percent elution will be closer to the 6th hour than the 22nd hour. Elution is generally enhanced by increasing the concentration and pH of the eluants, and combining the eluants.

  3. PRELIMINARY REPORT ON EVALUATION OF POTENTIAL ELUANTS FOR NON-ACID ELUTION OF CESIUM FROM RESORCINOL-FORMALDEHYDE RESIN

    SciTech Connect (OSTI)

    Adu-Wusu, K.; Pennebaker, F.

    2010-09-01T23:59:59.000Z

    Small-column ion exchange (SCIX) units installed in high-level waste tanks to remove Cs-137 from highly alkaline salt solutions are among the waste treatment plans in the DOE-complex. Spherical Resorcinol-Formaldehyde (sRF) is the ion exchange resin selected for use in the Hanford Waste Treatment and Immobilization Plant (WTP). It is also the primary ion exchange material under consideration for SCIX at the Hanford site. The elution step of the multi-step ion exchange process is typically done with 0.5 M nitric acid. An acid eluant is a potential hazard in the event of a spill, leak, etc. because the high-level waste tanks are made of carbon steel. Corrosion and associated structural damage may ensue. Studies are ongoing to explore non-acid elution as an alternative. Batch contact sorption equilibrium screening tests have been conducted with 36 potential non-acid eluants. The sorption tests involve equilibrating each cesium-containing eluant solution with the sRF resin for 48 hours at 25 C in a shaker oven. In the sorption tests, an eluant is deemed to have a high cesium elution potential if it minimizes cesium sorption onto the sRF resin. The top candidates (based on lowest cesium sorption distribution coefficients) include ammonium carbonate, ammonium carbonate/ammonium hydroxide, ammonium bicarbonate, rubidium carbonate, ammonium acetate, ammonium acetate/ammonium hydroxide, ammonium bicarbonate/ammonium hydroxide, calcium chloride, and magnesium chloride. The next phase of testing for this work will focus on the following down selected eluants: Ammonium carbonate, ammonium acetate, calcium acetate, magnesium acetate, nitric acid, and ammonium hydroxide. The next testing phase is a confirmation of the elution ability of the selected eluants. It will mimic a typical sRF cesium ion exchange process i.e., sorption or loading, caustic wash, water rinse, and elution via batch contact sorption and quasi column caustic wash/water rinse/elution. Due to corrosion concerns, calcium acetate and magnesium acetate will be tested instead of calcium chloride and magnesium chloride respectively. Nitric acid is for benchmarking since it is the baseline sRF eluant. The information at hand indicates ammonium hydroxide, while a weak base, may hold promise as an effective eluant. Hence, its inclusion among the eluants to be studied despite the fact that it was not tested as a stand-alone eluant earlier.

  4. Improved Approximations for Max Set Splitting and Max NAE SAT

    E-Print Network [OSTI]

    Ye, Yinyu

    Improved Approximations for Max Set Splitting and Max NAE SAT #3; Jiawei Zhang and Yinyu Ye y Nanjing, 210093, P.R.China August 16, 2000, Revised January 22, 2001. #3; This research was supported Fudan University, Shanghai, R.R.China. z This work was done while the author was visiting Computational

  5. Sequential elution process

    DOE Patents [OSTI]

    Kingsley, Ilse S. (Bethlehem, PA)

    1987-01-01T23:59:59.000Z

    A process and apparatus for the separation of complex mixtures of carbonaceous material by sequential elution with successively stronger solvents. In the process, a column containing glass beads is maintained in a fluidized state by a rapidly flowing stream of a weak solvent, and the sample is injected into this flowing stream such that a portion of the sample is dissolved therein and the remainder of the sample is precipitated therein and collected as a uniform deposit on the glass beads. Successively stronger solvents are then passed through the column to sequentially elute less soluble materials.

  6. Sequential elution process

    DOE Patents [OSTI]

    Kingsley, I.S.

    1987-01-06T23:59:59.000Z

    A process and apparatus are disclosed for the separation of complex mixtures of carbonaceous material by sequential elution with successively stronger solvents. In the process, a column containing glass beads is maintained in a fluidized state by a rapidly flowing stream of a weak solvent, and the sample is injected into this flowing stream such that a portion of the sample is dissolved therein and the remainder of the sample is precipitated therein and collected as a uniform deposit on the glass beads. Successively stronger solvents are then passed through the column to sequentially elute less soluble materials. 1 fig.

  7. CX-008371: Categorical Exclusion Determination

    Broader source: Energy.gov [DOE]

    Non-Acid Elution (NAE) of Cesium From Resorcinol-Formaldehyde Resin CX(s) Applied: B3.6 Date: 03/27/2012 Location(s): South Carolina Offices(s): Savannah River Operations Office

  8. CX-005500: Categorical Exclusion Determination

    Broader source: Energy.gov [DOE]

    Non-Acid Elution (NAE) of Cesium From Resorcinol-Formaldehyde ResinCX(s) Applied: B3.6Date: 02/24/2011Location(s): Aiken, South CarolinaOffice(s): Environmental Management, Savannah River Operations Office

  9. Gradient elution in capillary electrochromatography

    SciTech Connect (OSTI)

    Anex, D.; Rakestraw, D.J. [Sandia National Labs., Livermore, CA (United States); Yan, Chao; Dadoo, R.; Zare, R.N. [Stanford Univ., CA (United States). Dept. of Chemistry

    1997-08-01T23:59:59.000Z

    In analogy to pressure-driven gradient techniques in high-performance liquid chromatography, a system has been developed for delivering electroosmotically-driven solvent gradients for capillary electrochromatography (CEC). Dynamic gradients with sub-mL/min flow rates are generated by merging two electroosmotic flows that are regulated by computer-controlled voltages. These flows are delivered by two fused-silica capillary arms attached to a T-connector, where they mix and then flow into a capillary column that has been electrokinetically packed with 3-mm reversed-phase particles. The inlet of one capillary arm is placed in a solution reservoir containing one mobile phase and the inlet of the other is placed in a second reservoir containing a second mobile phase. Two independent computer-controlled programmable high-voltage power supplies (0-50 kV)--one providing an increasing ramp and the other providing a decreasing ramp--are used to apply variable high-voltage potentials to the mobile phase reservoirs to regulate the electroosmotic flow in each arm. The ratio of the electroosmotic flow rates between the two arms is changed with time according to the computer-controlled voltages to deliver the required gradient profile to the separation column. Experiments were performed to confirm the composition of the mobile phase during a gradient run and to determine the change of the composition in response to the programmed voltage profile. To demonstrate the performance of electroosmotically-driven gradient elution in CEC, a mixture of 16 polycyclic aromatic hydrocarbons (PAHs) was separated in less than 90 minutes. This gradient technique is expected to be well-suited for generating not only solvent gradients in CEC, but also other types of gradients such as pH- and ionic-strength gradients in capillary electrokinetic separations and analyses.

  10. Improved peptide elution time prediction for reversed-phase liquid...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    peptide elution time prediction for reversed-phase liquid chromatography-MS by incorporating peptide sequence Improved peptide elution time prediction for reversed-phase liquid...

  11. Innovative Elution Processes for Recovering Uranium from Seawater

    SciTech Connect (OSTI)

    Wai, Chien; Tian, Guoxin; Janke, Christopher

    2014-05-29T23:59:59.000Z

    Utilizing amidoxime-based polymer sorbents for extraction of uranium from seawater has attracted considerable interest in recent years. Uranium collected in the sorbent is recovered typically by elution with an acid. One drawback of acid elution is deterioration of the sorbent which is a significant factor that limits the economic competitiveness of the amidoxime-based sorbent systems for sequestering uranium from seawater. Developing innovative elution processes to improve efficiency and to minimize loss of sorbent capacity become essential in order to make this technology economically feasible for large-scale industrial applications. This project has evaluated several elution processes including acid elution, carbonate elution, and supercritical fluid elution for recovering uranium from amidoxime-based polymer sorbents. The elution efficiency, durability and sorbent regeneration for repeated uranium adsorption- desorption cycles in simulated seawater have been studied. Spectroscopic techniques are used to evaluate chemical nature of the sorbent before and after elution. A sodium carbonate-hydrogen peroxide elution process for effective removal of uranium from amidoxime-based sorbent is developed. The cause of this sodium carbonate and hydrogen peroxide synergistic leaching of uranium from amidoxime-based sorbent is attributed to the formation of an extremely stable uranyl peroxo-carbonato complex. The efficiency of uranium elution by the carbonate-hydrogen peroxide method is comparable to that of the hydrochloric acid elution but damage to the sorbent material is much less for the former. The carbonate- hydrogen peroxide elution also does not need any elaborate step to regenerate the sorbent as those required for hydrochloric acid leaching. Several CO2-soluble ligands have been tested for extraction of uranium from the sorbent in supercritical fluid carbon dioxide. A mixture of hexafluoroacetylacetone and tri-n-butylphosphate shows the best result but uranium removal from the sorbent reaches only 80% after 10 hours of leaching. Some information regarding coordination of vanadium with amidoxime molecules and elution of vanadium from amidoxime- based sorbents is also given in the report.

  12. E-Print Network 3.0 - automated elution time Sample Search Results

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    feedback delay and short elution time. Accurate constant-activity elutions of 10... infusion to the patient with an automated generator elution system 2. 82 Sr82 Rb generators...

  13. ELUTIONS Inc formerly TeCom | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 NoPublic Utilities Address:011-DNA Jump37. It is classified as ASHRAEDuval County,EEnergy(Redirected fromELUTIONS Inc

  14. Numerical modeling of elution peak profiles in supercritical fluid chromatography. Part I-Elution of an unretained tracer

    SciTech Connect (OSTI)

    Kaczmarski, Krzysztof [University of Tennessee and Rzeszow University of Technology, Poland; Guiochon, Georges A [ORNL

    2010-01-01T23:59:59.000Z

    When chromatography is carried out with high-density carbon dioxide as the main component of the mobile phase (a method generally known as 'supercritical fluid chromatography' or SFC), the required pressure gradient along the column is moderate. However, this mobile phase is highly compressible and, under certain experimental conditions, its density may decrease significantly along the column. Such an expansion absorbs heat, cooling the column, which absorbs heat from the outside. The resulting heat transfer causes the formation of axial and radial gradients of temperature that may become large under certain conditions. Due to these gradients, the mobile phase velocity and most physico-chemical parameters of the system (viscosity, diffusion coefficients, etc.) are no longer constant throughout the column, resulting in a loss of column efficiency, even at low flow rates. At high flow rates and in serious cases, systematic variations of the retention factors and the separation factors with increasing flow rates and important deformations of the elution profiles of all sample components may occur. The model previously used to account satisfactorily for the effects of the viscous friction heating of the mobile phase in HPLC is adapted here to account for the expansion cooling of the mobile phase in SFC and is applied to the modeling of the elution peak profiles of an unretained compound in SFC. The numerical solution of the combined heat and mass balance equations provides temperature and pressure profiles inside the column, and values of the retention time and efficiency for elution of this unretained compound that are in excellent agreement with independent experimental data.

  15. Alternate Methods for Eluting Cesium from Spherical Resorcinol-Formaldehyde Resin

    SciTech Connect (OSTI)

    Taylor, Paul Allen [ORNL; Johnson, Heather Lauren [University of Tennessee, Knoxville (UTK)

    2009-02-01T23:59:59.000Z

    A small-column ion exchange (SCIX) system has been proposed for removing cesium from the supernate and dissolved salt solutions in the high-level-waste tanks at the Savannah River Site (SRS). The SCIX system could use either crystalline silicotitanate (CST), an inorganic, non-regenerable sorbent, or spherical resorcinol-formaldehyde (RF), a new regenerable resin, to remove cesium from the waste solutions. The baseline method for eluting the cesium from the RF resin uses 15 bed volumes (BV) of 0.5 M nitric acid (HNO{sub 3}). The nitric acid eluate, containing the radioactive cesium, would be combined with the sludge from the waste tanks and would be converted into glass at the Defense Waste Processing Facility (DWPF) at SRS. The amount of nitric acid that would be used to elute the RF resin, using the current elution protocol, exceeds the capacity of DWPF to destroy the nitrate ions and maintain the required chemical reducing environment in the glass melt. Installing a denitration evaporator at SRS is technically feasible but would add considerable cost to the project. Alternate methods for eluting the resin have been tested, including using lower concentrations of nitric acid, other acids, and changing the flow regimes. About 4 BV of 0.5 M HNO{sub 3} are required to remove the sodium (titrate the resin) and most of the cesium from the resin, so the bulk of the acid used for the baseline elution method removes a very small quantity of cesium from the resin. A summary of the elution methods that have been tested are listed.

  16. Small-Column Cesium Ion Exchange Elution Testing of Spherical Resorcinol-Formaldehyde

    SciTech Connect (OSTI)

    Brown, Garrett N.; Russell, Renee L.; Peterson, Reid A.

    2011-10-21T23:59:59.000Z

    This report summarizes the work performed to evaluate multiple, cesium loading, and elution cycles for small columns containing SRF resin using a simple, high-level waste (HLW) simulant. Cesium ion exchange loading and elution curves were generated for a nominal 5 M Na, 2.4E-05 M Cs, 0.115 M Al loading solution traced with 134Cs followed by elution with variable HNO3 (0.02, 0.07, 0.15, 0.23, and 0.28 M) containing variable CsNO3 (5.0E-09, 5.0E-08, and 5.0E-07 M) and traced with 137Cs. The ion exchange system consisted of a pump, tubing, process solutions, and a single, small ({approx}15.7 mL) bed of SRF resin with a water-jacketed column for temperature-control. The columns were loaded with approximately 250 bed volumes (BVs) of feed solution at 45 C and at 1.5 to 12 BV per hour (0.15 to 1.2 cm/min). The columns were then eluted with 29+ BVs of HNO3 processed at 25 C and at 1.4 BV/h. The two independent tracers allowed analysis of the on-column cesium interaction between the loading and elution solutions. The objective of these tests was to improve the correlation between the spent resin cesium content and cesium leached out of the resin in subsequent loading cycles (cesium leakage) to help establish acid strength and purity requirements.

  17. Everolimus-induced Pneumonitis after Drug-eluting Stent Implantation: A Case Report

    SciTech Connect (OSTI)

    Sakamoto, Susumu, E-mail: susumu1029@gmail.com; Kikuchi, Naoshi; Ichikawa, Atsuo; Sano, Go; Satoh, Keita; Sugino, Keishi; Isobe, Kazutoshi; Takai, Yujiro [Toho University School of Medicine, Department of Respiratory Medicine (Japan); Shibuya, Kazutoshi [Toho University School of Medicine, Department of Pathology (Japan); Homma, Sakae [Toho University School of Medicine, Department of Respiratory Medicine (Japan)

    2013-08-01T23:59:59.000Z

    Despite the wide use of everolimus as an antineoplastic coating agent for coronary stents to reduce the rate of restenosis, little is known about the health hazards of everolimus-eluting stents (EES). We describe a case of pneumonitis that developed 2 months after EES implantation for angina. Lung pathology demonstrated an organizing pneumonia pattern that responded to corticosteroid therapy. Although the efficacy of EES for ischemic heart disease is well established, EES carries a risk of pneumonitis.

  18. Comparing long-term antiplatelet strategies to prevent morbidity and mortality in patients with drug-eluting coronary stents

    E-Print Network [OSTI]

    Evans, J. Stewart (James Stewart)

    2010-01-01T23:59:59.000Z

    Background: The optimal long-term antiplatelet therapy (APT) that balances the benefit of preventing myocardial infarction (MI) with the risk of severe bleeding is unknown in patients greater than one year after drug-eluting ...

  19. USE OF DRUG ELUTING STENTS AS A FUNCTION OF PREDICTED BENEFIT: CLINICAL AND ECONOMIC IMPLICATIONS OF CURRENT PRACTICE

    E-Print Network [OSTI]

    Amin, Amit P.

    2011-12-31T23:59:59.000Z

    Background: Benefits of drug-eluting stents (DES) in percutaneous coronary intervention (PCI) are greatest in those at the highest risk of target vessel revascularization (TVR). While DES reduce restenosis, they cost more than bare metal stents (BMS...

  20. Numerical modeling of the elution peak profiles of retained solutes in supercritical fluid chromatography

    SciTech Connect (OSTI)

    Kaczmarski, Krzysztof [University of Tennessee and Rzeszow University of Technology, Poland; Guiochon, Georges A [ORNL

    2011-01-01T23:59:59.000Z

    In supercritical fluid chromatography (SFC), the significant expansion of the mobile phase along the column causes the formation of axial and radial gradients of temperature. Due to these gradients, the mobile phase density, its viscosity, its velocity, its diffusion coefficients, etc. are not constant throughout the column. This results in a nonuniform flow velocity distribution, itself causing a loss of column efficiency in certain cases, even at low flow rates, as they do in HPLC. At high flow rates, an important deformation of the elution profiles of the sample components may occur. The model previously used to account satisfactorily for the retention of an unsorbed solute in SFC is applied to the modeling of the elution peak profiles of retained compounds. The numerical solution of the combined heat and mass balance equations provides the temperature and the pressure profiles inside the column and values of the retention time and the band profiles of retained compounds that are in excellent agreement with independent experimental data for large value of mobile phase reduced density. At low reduced densities, the band profiles can strongly depend on the column axial distribution of porosity.

  1. NAE National Meeting Thursday February 7, 2013

    E-Print Network [OSTI]

    Zhou, Chongwu

    " "" """ "" """ "Our Times" Yannis C. Yortsos University of Southern California #12;"This is the most #12;» Make Solar Energy Economical " » Provide Energy from Fusion" » Develop Carbon Sequestration environmental stresses, but also with the capacity to generate new challenges

  2. Radiosensitizer-eluting nanocoatings on gold fiducials for biological in-situ image-guided radio therapy (BIS-IGRT)

    E-Print Network [OSTI]

    Sridhar, Srinivas

    -eluting nanocoatings on gold fiducials for biological in-situ image-guided radio therapy (BIS-IGRT) D K Nagesha1,3 , D, an initial release within the first few hours was followed by a sustained release over the course of the next-9155/10/206039+14$30.00 © 2010 Institute of Physics and Engineering in Medicine Printed in the UK 6039 #12;6040 D K Nagesha et al

  3. A Budget Impact Model for Paclitaxel-eluting Stent in Femoropopliteal Disease in France

    SciTech Connect (OSTI)

    De Cock, Erwin, E-mail: erwin.decock@unitedbiosource.com [United BioSource Corporation, Peri- and Post-Approval Services (Spain); Sapoval, Marc, E-mail: Marc.sapoval2@egp.aphp.fr [Hopital Europeen Georges Pompidou, Universite Rene Descartes, Department of Cardiovascular and Interventional Radiology (France)] [Hopital Europeen Georges Pompidou, Universite Rene Descartes, Department of Cardiovascular and Interventional Radiology (France); Julia, Pierre, E-mail: pierre.julia@egp.aphp.fr [Hopital Europeen Georges Pompidou, Universite Rene Descartes, Cardiovascular Surgery Department (France)] [Hopital Europeen Georges Pompidou, Universite Rene Descartes, Cardiovascular Surgery Department (France); Lissovoy, Greg de, E-mail: gdelisso@jhsph.edu [Johns Hopkins Bloomberg School of Public Health, Department of Health Policy and Management (United States); Lopes, Sandra, E-mail: Sandra.Lopes@CookMedical.com [Cook Medical, Health Economics and Reimbursement (Denmark)] [Cook Medical, Health Economics and Reimbursement (Denmark)

    2013-04-15T23:59:59.000Z

    The Zilver PTX drug-eluting stent (Cook Ireland Ltd., Limerick, Ireland) represents an advance in endovascular treatments for atherosclerotic superficial femoral artery (SFA) disease. Clinical data demonstrate improved clinical outcomes compared to bare-metal stents (BMS). This analysis assessed the likely impact on the French public health care budget of introducing reimbursement for the Zilver PTX stent. A model was developed in Microsoft Excel to estimate the impact of a progressive transition from BMS to Zilver PTX over a 5-year horizon. The number of patients undergoing SFA stenting was estimated on the basis of hospital episode data. The analysis from the payer perspective used French reimbursement tariffs. Target lesion revascularization (TLR) after primary stent placement was the primary outcome. TLR rates were based on 2-year data from the Zilver PTX single-arm study (6 and 9 %) and BMS rates reported in the literature (average 16 and 22 %) and extrapolated to 5 years. Net budget impact was expressed as the difference in total costs (primary stenting and reinterventions) for a scenario where BMS is progressively replaced by Zilver PTX compared to a scenario of BMS only. The model estimated a net cumulative 5-year budget reduction of Euro-Sign 6,807,202 for a projected population of 82,316 patients (21,361 receiving Zilver PTX). Base case results were confirmed in sensitivity analyses. Adoption of Zilver PTX could lead to important savings for the French public health care payer. Despite higher initial reimbursement for the Zilver PTX stent, fewer expected SFA reinterventions after the primary stenting procedure result in net savings.

  4. Systematic Review of Infrapopliteal Drug-Eluting Stents: A Meta-Analysis of Randomized Controlled Trials

    SciTech Connect (OSTI)

    Katsanos, Konstantinos, E-mail: katsanos@med.upatras.gr [NHS Foundation Trust, King's Health Partners, Department of Interventional Radiology, Guy's and St. Thomas' Hospitals (United Kingdom); Spiliopoulos, Stavros [Patras University Hospital, Department of Interventional Radiology, School of Medicine (Greece); Diamantopoulos, Athanasios [NHS Foundation Trust, King's Health Partners, Department of Interventional Radiology, Guy's and St. Thomas' Hospitals (United Kingdom); Karnabatidis, Dimitris [Patras University Hospital, Department of Interventional Radiology, School of Medicine (Greece); Sabharwal, Tarun [NHS Foundation Trust, King's Health Partners, Department of Interventional Radiology, Guy's and St. Thomas' Hospitals (United Kingdom); Siablis, Dimitris [Patras University Hospital, Department of Interventional Radiology, School of Medicine (Greece)

    2013-06-15T23:59:59.000Z

    IntroductionDrug-eluting stents (DES) have been proposed for the treatment of infrapopliteal arterial disease. We performed a systematic review to provide a qualitative analysis and quantitative data synthesis of randomized controlled trials (RCTs) assessing infrapopliteal DES.Materials and MethodsPubMed (Medline), EMBASE (Excerpta Medical Database), AMED (Allied and Complementary medicine Database), Scopus, CENTRAL (Cochrane Central Register of Controlled Trials), online content, and abstract meetings were searched in September 2012 for eligible RCTs according to the preferred reporting items for systematic reviews and meta-analyses selection process. Risk of bias was assessed using the Cochrane Collaboration's tool. Primary endpoint was primary patency defined as absence of {>=}50 % vessel restenosis at 1 year. Secondary outcome measures included patient survival, limb amputations, change of Rutherford-Becker class, target lesion revascularization (TLR) events, complete wound healing, and event-free survival at 1 year. Risk ratio (RRs) were calculated using the Mantel-Haenszel fixed effects model, and number-needed-to-treat values are reported.ResultsThree RCTs involving 501 patients with focal infrapopliteal lesions were analyzed (YUKON-BTX, DESTINY, and ACHILLES trials). All three RCTs included relatively short and focal infrapopliteal lesions. At 1 year, there was clear superiority of infrapopliteal DES compared with control treatments in terms of significantly higher primary patency (80.0 vs. 58.5 %; pooled RR = 1.37, 95 % confidence interval [CI] = 1.18-1.58, p < 0.0001; number-needed-to-treat (NNT) value = 4.8), improvement of Rutherford-Becker class (79.0 vs. 69.6 %; pooled RR = 1.13, 95 % CI = 1.002-1.275, p = 0.045; NNT = 11.1), decreased TLR events (9.9 vs. 22.0 %; pooled RR = 0.45, 95 % CI = 0.28-0.73, p = 0.001; NNT = 8.3), improved wound healing (76.8 vs. 59.7 %; pooled RR = 1.29, 95 % CI = 1.02-1.62, p = 0.04; NNT = 5.9), and better overall event-free survival (72.2 vs. 57.3 %; pooled RR = 1.26, 95 % CI = 1.10-1.44, p = 0.0006; NNT = 6.7). Conclusion. DES for focal infrapopliteal lesions significantly inhibit vascular restenosis and thereby improve primary patency, decrease repeat procedures, improve wound healing, and prolong overall event-free survival.

  5. Column Experiments for Radionuclide Adsorption Studies of the Culebra Dolomite: Retardation Parameter Estimation for Non-Eluted Actinide Species

    SciTech Connect (OSTI)

    Brown, G.O.; Lucero, D.A.; Perkins, W.G.

    1999-01-01T23:59:59.000Z

    The U.S. Department of Energy (DOE) has been developing a nuclear waste disposal facility, the Waste Isolation Pilot Plant (WIPP), located approximately 42 km east of Carlsbad, New Mexico. The WIPP is designed to demonstrate the safe disposal of transuranic wastes produced by the defense nuclear-weapons program. Performance assessment analyses (U.S. DOE, 1996) indicate that human intrusion by inadvertent and intermittent drilling for resources provide the only credible mechanisms for significant releases of radionuclides horn the disposal system. These releases may occur by five mechanisms: (1) cuttings, (2) cavings, (3) spallings, (4) direct brine releases, and (5) long-term brine releases. The first four mechanisms could result in immediate release of contaminant to the accessible environment. For the last mechanism, migration pathways through the permeable layers of rock above the Salado are important, and major emphasis is placed on the Culebra Member of the Rustler Formation because this is the most transmissive geologic layer in the disposal system. For reasons of initial quantity, half-life, and specific radioactivity, certain isotopes of Th, U, Am, and Pu would dominate calculated releases from the WIPP. In order to help quanti~ parameters for the calculated releases, radionuclide transport experiments have been carried out using five intact-core columns obtained from the Culebra dolomite member of the Rustler Formation within the Waste Isolation Pilot Plant (WIPP) site in southeastern New Mexico. This report deals primarily with results of mathematical analyses related to the retardation of %J%, 24%, and 24'Am in two of these cores (B-Core - VPX26-11A and C-Core - VPX28-6C). All B-Core transport experiments were done using Culebra-simukmt brine relevant to the core recovery location (the WIPP air-intake shaft - AIS). Most experiments with C-Core were done with AIS brine with some admixture of a brine composition (ERDA-6) that simulated deeper formation brines. No significant changes in transport behavior were observed for changes in brine. Hydraulic characteristics (i.e., apparent porosity and apparent dispersion coefficient) for the cores were obtained via experiments using conservative tracer `Na. Elution experiments carried out over periods of a few days with tracers `*U and %Np indicated that these tracers were weakly retarded as indicated by delayed elution of these species. Elution experiments with tracers `%, 24'Pu, and 24'Ani were performed, but no elution of any of these species was observed in any flow experiment to date, including experiments of up to two years duration. However, B-Core was subjected to tomographic analysis from which a retardation factor can be inferred for%. Moreover, the fact of non- elution for 24*Pu and 24'Am after more than two years brine flow through C-Core can be coupled with the minimum detectable activity for each of these species to compute minimum retardation factors in C-Core. The retardation factors for all three species can then be coupled with the apparent hydraulic characteristics to estimate an apparent minimum solutionhock distribution coefficient, &, for each actinide. The specific radionuclide isotopes used in these experiments were chosen to facilitate analysis. Even though these isotopes are not necessarily the same as those that are most important to WIPP performance, they are isotopes of the same elements, and . their chemical and transport properties are therefore identical to those of isotopes in the WIPP inventory. The retardation factors and & values deduced from experimental results strongly support the contention that sorption in the Culebra provides an effective barrier to release of Th, Pu, and Am during the regulatory period.

  6. Los Alamos engineer selected to participate in NAE's 2012 "Frontiers...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    2006; master's, 2004; bachelor's, 2000) from the University of Maryland, College Park. He joined Los Alamos National Laboratory in the fall of 2006. The symposium is to be...

  7. ven as the National Academy of Engineering (NAE) announced its

    E-Print Network [OSTI]

    Simaan, Nabil

    the health and well being of the planet and quality of life. Challenges range from making solar energy Coast to the West Coast,"says George Cook, associate dean for research and graduate studies. Noting pieces of the solution areas. Environmental Concerns One top challenge is making solar energy affordable."Solar

  8. Fundamental chromatographic equations designed for columns packed with very fine particles and operated at very high pressures applications to the prediction of elution times and the column efficiencies

    SciTech Connect (OSTI)

    Gritti, Fabrice [University of Tennessee, Knoxville (UTK); Guiochon, Georges A [ORNL

    2008-01-01T23:59:59.000Z

    The wall temperatures of three Acquity-BEH-C{sub 18}columns (2.1 mm x 50, 100, and 150 mm) and the temperature of the incoming eluent were maintained constant at 289 K, using a circulating water heat exchanger. The retention times and the band broadening of naphtho[2,3-a]pyrene were measured for each column as a function of the flow rate applied. Pure acetonitrile was used as the eluent. The flow rate dependence of neither elution volumes nor bandwidths can be accounted for by classical models of retention and HETP, respectively, since these models assume columns to be isothermal. Because the heat generated by friction of the eluent against the column bed increases with increasing flow rate, the column bed cannot remain isothermal at high flow rates. This heat is evacuated radially and/or longitudinally by convection, conduction, and radiation. Radial and axial temperature gradients are formed, which are maximum and minimum, respectively, when the temperature of the column wall is kept uniform and constant. The retention times that we measured match well with the values predicted based on the temperature distribution along and across the column, which we calculated and on the temperature dependence of the retention for the same column operated isothermally (i.e., at very low flow rate). The rate of band spreading varies along non-isothermal columns, so the HETP can only be defined locally. It is a function of the axial coordinate. A new contribution is needed to account for the radial thermal heterogeneity of the column, hence the radial distribution of the flow velocities, which warps the elution band. A new model, based on the general dispersion theory of Aris, allows a successful prediction of the unusually large bandwidths observed with columns packed with fine particles, operated at high flow rates, hence high inlet pressures.

  9. USCViterbi//Engineer USC'S NEW PRESIDENT // NAE GRAND CHALLENGES SUMMIT // HEALTH CARE VIA MOBILE PHONE

    E-Print Network [OSTI]

    Zhou, Chongwu

    Pulsed Power Group is experimenting with plasma ignition to develop cleaner, more efficient diesel.0 PARTICLES 4 Diesel Emissions 5 Power Cell Phones 20

  10. NAS-NAE National Convocation on "Rising Above the Gathering Storm...

    Energy Savers [EERE]

    fortunate position of "preaching to the choir" today. After all, there are few things we care more passionately about than the need to strengthen America's position in the world...

  11. Introduction In the year 2000 the National Academy of Engineering (NAE) issued the

    E-Print Network [OSTI]

    Heller, Barbara

    of homes and businesses, clean water, refrigeration and air conditioning), as well as advances Institute of Technology (IIT) and Chicago Council on Science and Technology (C2ST), along with our academic of the 14 Grand Challenges: clean water; carbon, energy and climate; urban sustainability; and global

  12. NAS-NAE National Convocation on "Rising Above the Gathering Storm Two Years

    Energy Savers [EERE]

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Delicious RankCombustion |EnergyonSupport0.pdf5 OPAM SEMIANNUAL REPORTMAMayCrossColoradoMotionMunicipalCodesLater:

  13. Los Alamos engineer selected to participate in NAE's 2012 "Frontiers of

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsrucLas Conchas recovery challenge fund Las Conchas recovery challengeEngineering"

  14. Current Research at BBISS John C. Crittenden, Ph.D., N.A.E., P.E.

    E-Print Network [OSTI]

    Das, Suman

    Economic Analysis Sergiy Smetana PhD, CEE Fulbright Scholar Visiting Student, Institute of NatureD, CEE Sichuan University Electrochemical degradation of organic pollutants. Yuheng Feng Visiting Student, PhD, CEE Zhejian University Catalytic degradation of dioxin using computational chemistry. Xia Yang

  15. affect antibiotic elution: Topics by E-print Network

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    volume, sorbate and sorbent concentration and it is independence to temperature. Then the isotherm models were used to explain the sorption process and the outcomes reveal that...

  16. Phosphopeptide elution times in reversed-phase liquid chromatography. |

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear Security Administration the1 - September 2006 TheSteven AshbyDepartmentPersonnelAdams5EMSLBluetheoretical

  17. Improved peptide elution time prediction for reversed-phase liquid

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation ProposedUsingFun withconfinementEtching.348 270 300 219 255Retrievals ofchromatography-MS by

  18. Curriculum Vitae for John C. Crittenden, Ph.D., P.E., N.A.E. (Revised: 6/11/2014)

    E-Print Network [OSTI]

    Jacobs, Laurence J.

    ). Director, Center for Clean Industrial and Treatment Technology, an EPA Funded Research Center of Excellence Technologies School of Civil and Environmental Engineering 828 West Peachtree, Suite 320B Atlanta Systems, Professor of Civil and Environmental Engineering, Georgia Institute of Technology (January 1

  19. Modeling Elution Histories of Copper and Lead from Contaminated Soil Treated by Poly,,amidoamine... Dendrimers

    E-Print Network [OSTI]

    Clement, Prabhakar

    procedures; Heavy metals; Soil pollution; Soil treatment. In recent years, extraction of heavy metals from transport models do not simulate the dynamic leaching process of heavy metals desorbed by the water soluble soil treated by poly amidoamine dendrimers. In the model, the metal sorption sites of the soil were

  20. Selection of the Optimum Electrospray Voltage for Gradient Elution LC-MS

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear Security Administrationcontroller systemsBi (2) SrEvaluating the Seasonalsw ' b(SC)

  1. NETL-RUA Annual Review FY2012 DOE/NETL-2012/1579 National Energy...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    NAE National Academy of Engineering NAS National Academy of Sciences NATCARB National Carbon Sequestration Database and Geographic Information System NETL National Energy...

  2. Transcatheter Arterial Chemoembolization (TACE) of Colorectal Cancer Liver Metastases by Irinotecan-Eluting Microspheres in a Salvage Patient Population

    SciTech Connect (OSTI)

    Huppert, Peter, E-mail: huppert@klinikum-darmstadt.de [Klinikum Darmstadt GmbH, Department of Diagnostic and Interventional Radiology (Germany); Wenzel, Thorsten [Klinikum Darmstadt GmbH, Department of Medical Oncology (Germany); Wietholtz, Hubertus [Klinikum Darmstadt GmbH, Department of Gastroenterology (Germany)

    2013-05-14T23:59:59.000Z

    PurposeThis prospective study evaluated the effectiveness and safety of TACE using irinotecan loaded superabsorbent polymer (SAP) microspheres for treatment of colorectal cancer liver metastases (CCLM) in a salvage setting of patients.MethodsA total of 71 TACE procedures were performed in 29 patients with liver only or liver-dominant CCLM. In all patients, systemic chemotherapy before TACE had failed. Two hundred milligrams of irinotecan were loaded into 50100mg of SAP microspheres (HepaSphere Microspheres) considering tumor size and vascularization. TACE was performed selectively with respect to tumor distribution. Response was evaluated following RECIST and EASL criteria, respectively. Median follow-up after last TACE was 8 (range 154) months. All patients had died at time of analysis.ResultsAll TACE procedures were performed successfully; 35400mg (mean 168.3mg) of irinotecan loaded in 13100mg (mean 48.3mg) SAP microspheres were injected during individual sessions. No major complications occurred. Three, 6, and 12months after first TACE complete and partial response was present in 72, 32%, 0 of patients by EASL criteria and stable disease was seen in 86, 48, and 8% with no complete and no partial response by RECIST criteria. Median overall survival after first TACE was 8months, and median time to progression was 5months. Median overall survival was longer in patients with limited (<25%) compared with extensive (>50%) intrahepatic disease (21 vs. 5months, p<0.005).ConclusionsTACE using irinotecan loaded SAP microspheres is safe and effective in terms of tumor necrosis. Survival benefit in a salvage setting seems to be limited in patients with advanced intrahepatic tumor load.

  3. Transarterial Chemoembolization of Unresectable Hepatocellular Carcinoma with Drug Eluting Beads: Results of an Open-Label Study of 62 Patients

    SciTech Connect (OSTI)

    Malagari, Katerina, E-mail: kmalag@acn.gr; Chatzimichael, Katerina; Alexopoulou, Efthymia; Kelekis, Alexios [University of Athens, Second Department of Radiology (Greece); Hall, Brenda [Biocompatibles UK, Inc. (United Kingdom); Dourakis, Spyridon [University of Athens, and Department of Internal Medicine and Hepatology, Ippokration Hospital University of Athens, Second Clinic of Internal Medicine and Hepatology (Greece); Delis, Spyridon [Agia Olga Hospital, Department of Surgery (Greece); Gouliamos, Athanasios [University of Athens, Second Department of Radiology (Greece); Kelekis, Dimitrios [University of Athens, Evgenidion Hospital, Research Centre of Radiology and Imaging (Greece)

    2008-03-15T23:59:59.000Z

    The purpose of this study was to assess the safety and efficacy of doxorubicin-loaded beads (DC Beads) delivered by transarterial embolization for the treatment of unresectable hepatocellular carcinoma (HCC). This open-label, single-center, single-arm study included 62 cirrhotic patients with documented single unresectable HCC. Mean tumor diameter was 5.6 cm (range, 3-9 cm) classified as Okuda stages 1 (n = 53) and 2 (n = 9). Patients received repeat embolizations with doxorubicin-loaded beads every 3 months (maximum of three). The maximum doxorubicin dose was 150 mg per embolization, loaded in DC Beads of 100-300 or 300-500 {mu}m. Regarding efficacy, overall, an objective response according to the European Association for the Study of the Liver criteria was observed in 59.6%, 81.8%, and 70.8% across three treatments. A complete response was observed in 4.8% after the first procedure and 3.6% and 8.3% after the second and third procedures, respectively. At 9 months a complete response was seen in 12.2%, an objective response in 80.7%, progressive disease in 6.8%, and 12.2% showed stable disease. Mean tumor necrosis ranged from 77.4% to 83.9% (range, 28.6%-100%) across three treatments. {alpha}-Fetoprotein levels showed a mean decrease of 1123 ng/ml (95% CI = 846-1399; p = 3 x 10{sup -11}) after the first session and remained stable after the second and third embolizations (42 and 70 ng/ml decrease, respectively). Regarding safety, bilirubin, {gamma}-glutamyl transferase, aspartate aminotransferase, alanine aminotransferase, and alkaline phosphatase showed only transient increases during the study period. Severe procedure-related complications were seen in 3.2% (cholecystitis, n 1; liver abscess, n = 1). Postembolization syndrome was observed in all patients. We conclude that hemoembolization using doxorubicin-loaded DC Beads is a safe and effective treatment of HCC as demonstrated by the low complication rate, increased tumor response, and sustained reduction of {alpha}-fetoprotein levels.

  4. The Role of Neutron Activation Analysis in the Pathological Evaluation of Silver-Eluting Biomedical Devices in Biological Matrices

    E-Print Network [OSTI]

    Lancon, Trevor

    2014-08-14T23:59:59.000Z

    to their presence was not observed. INAA results correlated with these findings; silver was not detected adjacent to the test article, but a concentration of 74 ppm 29% of silver was observed in tissue adjacent to the control article. A complex system of ordinary...

  5. Preparing Women and Minorities for Science and Engineering: Resources for Educators, Parents, and the Community

    E-Print Network [OSTI]

    Dyer, Bill

    . The companion site Celebration of Women in Engineering http://www.nae.edu/nae/cwe/cwemain.nsf offers resources and pursuit of engineering careers. The inter-linked sites are part of the National Academy of Engineering on Women in Science and Engineering web site http://www4.nationalacademies.org

  6. Design Editorial Design: The New Frontier

    E-Print Network [OSTI]

    Papalambros, Panos

    Journal of Mechanical Design Editorial Design: The New Frontier An increasingly well to 2009 NAE Inductee Class, http://www.nae.edu/18185.aspx . This linking is the new frontier for sustainable growth and innovation, and design is the surest path to realizing it. Design is the new frontier

  7. Infusing Real World Experiences into ENGINEERING

    E-Print Network [OSTI]

    Napier, Terrence

    Infusing Real World Experiences into ENGINEERING EDUCATION #12;This project is a collaboration with the authors and NAE. #12;Infusing Real World Experiences into Engineering Education 2012 #12;2 Preface The aim

  8. Annual Energy Outlook 2013

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    NAE-AAES Convocation of the Professional Engineering Societies April 28, 2014 | Washington, DC By Adam Sieminski, EIA Administrator The U.S. has experienced a rapid increase in...

  9. Being water-sensi-ve to improve `liveability' Prof David Pannell

    E-Print Network [OSTI]

    pollutants ­ keeps them out of waterways & estuaries · Stormwater management · Na;es 2012 Combining water sources · Groundwater · Dams · Desal · Recycling · Rainwater

  10. Accounting for the mortality benefit of drug-eluting stents in percutaneous coronary intervention: a comparison of methods in a retrospective cohort study

    E-Print Network [OSTI]

    Yeh, Robert W; Chandra, Malini; McCulloch, Charles E; Go, Alan S

    2011-01-01T23:59:59.000Z

    stents in percutaneous coronary intervention: a comparisonstents in percutaneous coronary intervention: a comparisonoutcomes after percutaneous coronary intervention (PCI) with

  11. 1.1 0.2 were bound to the column and were eluted by 30 mM and 1 M HCI, respec-

    E-Print Network [OSTI]

    Boyer, Edmond

    infusion on postabsorp- tive glycemia in non insulin dependent diabetes mellitus (NIDDM). V Rigalleau previously reported a hyper- glycemic effect of a lipid infusion in the postabsorptive state in NIDD patients patients. Fifteen received a 180 min lipid infusion (')veiip20%'; 0.0155 mUkg/min) and 15 received saline

  12. The freezing threshold for k-colourings of a random graph Michael Molloy

    E-Print Network [OSTI]

    Molloy, Mike

    to determine the freezing threshold of most random CSP's for which we can use the planted model, eg. NAE much of the progress on random constraint satisfaction problems (CSP's). In particular, a common the cluster. These hypotheses have impacted the study of random CSP's in the theoretical computer science

  13. Top Engineers to Investigate Cause of Oil by Lauren Schenkman on July 13, 2010 6:02 PM |

    E-Print Network [OSTI]

    Southern California, University of

    in the nuclear power, aviation, and petrochemical industries. · M. Elisabeth Paté-Cornell, Burt and Deedee McTop Engineers to Investigate Cause of Oil Spill by Lauren Schenkman on July 13, 2010 6:02 PM | Investigations into the gulf oil disaster are multiplying. The National Academy of Engineering (NAE

  14. Commencement Program, May 19, 2013

    E-Print Network [OSTI]

    2013-05-19T23:59:59.000Z

    with CONSISTENCY. Maya Angelou Without COURAGE, 18 Awards Class of 2013 Awards Donald K. Alderson Memorial Award Bryan Trong Do Hannah Marie Bolton Samuel Philip Schroeder Agnes Wright Strickland Award Matthew Brian Moore Caryl K. Smith Student Leader... Michelle Lea Mubarak Bernadette Ann Myers Alexandra Ruth Orr Brandie LeNae Rhodes Kay Anne Riedl Jessica Jasmine Roach Ursula Rachel Rothrock Kara Khrystine Schippers Sarah Jane Shier Kathryn Lee Songer Jenna Michelle Steffen Sarah Mary Stern Danielle Dee...

  15. Enhanced drug delivery capabilities from stents coated with absorbable polymer and crystalline drug

    E-Print Network [OSTI]

    Carlyle, Wenda C.

    Current drug eluting stent (DES) technology is not optimized with regard to the pharmacokinetics of drug delivery. A novel, absorbable-coating sirolimus-eluting stent (AC-SES) was evaluated for its capacity to deliver drug ...

  16. NET PRED UTILITY

    Energy Science and Technology Software Center (OSTI)

    002602IBMPC00 Normalized Elution Time Prediction Utility http://omics.pnl.gov/software/NETPredictionUtility.php

  17. Monthly Progress Report No. 59 for March 1948

    E-Print Network [OSTI]

    2010-01-01T23:59:59.000Z

    europium, samarium, and promethium are eluted well ahead ofcome off ahead of promethium and possibly even ahead of

  18. Monthly Progress Report No. 59 for March 1948

    E-Print Network [OSTI]

    Various

    2008-01-01T23:59:59.000Z

    europium, samarium, and promethium are eluted well ahead ofcome off ahead of promethium and possibly even ahead of

  19. Decontamination, decommissioning, and vendor advertorial issue, 2007

    SciTech Connect (OSTI)

    Agnihotri, Newal (ed.)

    2007-07-15T23:59:59.000Z

    The focus of the July-August issue is on Decontamination, decommissioning, and vendor advertorials. Major articles/reports in this issue include: An interesting year ahead of us, by Tom Christopher, AREVA NP Inc.; U.S.-India Civil Nuclear Cooperation; Decontamination and recycling of retired components, by Sean P. Brushart, Electric Power Research Institute; and, ANO is 33 and going strong, by Tyler Lamberts, Entergy Nuclear Operations, Inc. The industry innovation article is: Continuous improvement process, by ReNae Kowalewski, Arkansas Nuclear One.

  20. Centipedes and Millipedes

    E-Print Network [OSTI]

    Brown, Wizzie

    2004-09-17T23:59:59.000Z

    and are commonly found in soil or leaf litter and under rocks or wood. Description Both centipedes and millipedes have long, segmented bodies connected to heads with a single pair of anten- nae. Centipedes vary from brown to grey to red to green- ish..., protected habitats, for example, under stones, rotted logs, leaves or bark. Although a few species give birth to live young, most centipedes lay eggs in soil during the warm months. The eggs are covered by a sticky substance. Centipedes are predators...

  1. Some properties of the Goncarov polynomials

    E-Print Network [OSTI]

    Eldred, Linda Mae

    1972-01-01T23:59:59.000Z

    of the Gonh'arov Polynomials. (May 1972) Linda Nae Eldred, B. A. , SUNY at Fredonia Directed by: Dr. Charles K. Chui In this thesis we collect from the known literature some important properties and applications of the GonKarov polynomials G ( z zp f z I... ) and the correspond ing constants R . Among n' other things, we also discuss the behavior of the G (z; zp p z I) for some specific parameters zp& z 1 ~ n-1 iv ACKNOWLEDGENENTS I wish to thank my committee chairman, Dr. Charles K. Chui, for his patience...

  2. North Shaokatan Wind Farm | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth's HeatMexico:Community NominationsCarolina‎ |NAE/Enel North America

  3. North Shore Mono Lake Geothermal Area | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth's HeatMexico:Community NominationsCarolina‎ |NAE/Enel North AmericaShore

  4. North Sky River | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth's HeatMexico:Community NominationsCarolina‎ |NAE/Enel North

  5. North Wilkes Middle and High School Wind Project | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth's HeatMexico:Community NominationsCarolina‎ |NAE/Enel NorthMiddle and High

  6. NorthWinds Renewables | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth's HeatMexico:Community NominationsCarolina‎ |NAE/Enel NorthMiddle and

  7. Northborough, Massachusetts: Energy Resources | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth's HeatMexico:Community NominationsCarolina‎ |NAE/Enel NorthMiddle

  8. Northeast - NY NJ CT PA Area | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth's HeatMexico:Community NominationsCarolina‎ |NAE/Enel NorthMiddleNortheast

  9. Northeast Advanced Vehicle Consortium NAVC | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth's HeatMexico:Community NominationsCarolina‎ |NAE/Enel

  10. Northern Arizona University Wind Project | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth's HeatMexico:Community NominationsCarolina‎ |NAE/EnelAZ Coordinates

  11. Northern Basin and Range Geothermal Region | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth's HeatMexico:Community NominationsCarolina‎ |NAE/EnelAZ Coordinates Jump

  12. Northern Colorado Wind Energy Center (GE) | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth's HeatMexico:Community NominationsCarolina‎ |NAE/EnelAZ Coordinates

  13. Northern Colorado Wind Energy Center (Siemens) | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth's HeatMexico:Community NominationsCarolina‎ |NAE/EnelAZ

  14. Northern Mariana Islands: Energy Resources | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth's HeatMexico:Community NominationsCarolina‎ |NAE/EnelAZMariana Islands:

  15. Northern Mariana Islands: Energy Resources | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth's HeatMexico:Community NominationsCarolina‎ |NAE/EnelAZMariana

  16. Northern States Metals Company | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth's HeatMexico:Community NominationsCarolina‎ |NAE/EnelAZMarianaMetals

  17. Northern States Power Co (Wisconsin) | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth's HeatMexico:Community NominationsCarolina‎ |NAE/EnelAZMarianaMetals

  18. Method of degrading trinitrotoluene

    DOE Patents [OSTI]

    Tyndall, R.L.; Vass, A.

    1996-01-16T23:59:59.000Z

    A method is disclosed of eluting trinitrotoluene (TNT) from soil using a dispersant from bacterial intra-amoebic isolate 1s, ATCC 75229.

  19. Method of degrading trinitrotoluene

    DOE Patents [OSTI]

    Tyndall, Richard L. (Clinton, TN); Vass, Arpad (Oak Ridge, TN)

    1996-01-01T23:59:59.000Z

    A method of eluting trinitrotoluene (TNT) from soil using a dispersant from bacterial intra-amoebic isolate 1s, ATCC 75229.

  20. STUDIES IN THE NUCLEAR CHEMISTRY OF PLUTONIUM, AMERICIUM, AND CURIUM AND MASSES OF THE HEAVIEST ELEMENTS

    E-Print Network [OSTI]

    Glass, Richard Alois

    2011-01-01T23:59:59.000Z

    CHEMISTRY OF PLUTONIUM, AMERICIUM, AND CURIUM AND THE MASSESTO ION EXCHANGE SEPARATIONS OF AMERICIUM AND CURIUM A. B.5. Tartrate elutions of americium and curium from Dowex-50

  1. El TRANSITION PROBABILITIES FROM Kn= O-AND Kn=1- STATES OF 238Pu

    E-Print Network [OSTI]

    Lederer, C. Michael

    2012-01-01T23:59:59.000Z

    ratio 1:8x1o-6 Americium and curium were separated fromthen separated from the americium by elution from a cation-

  2. Microsoft Word - DOE-ID-13-081 Idaho EC B3-6.doc

    Broader source: Energy.gov (indexed) [DOE]

    1 SECTION A. Project Title: Innovative Elution Processes for Recovering Uranium and Transition Metals from Amidoxime- based Sorbents - University of Idaho SECTION B. Project...

  3. CX-011544: Categorical Exclusion Determination | Department of...

    Broader source: Energy.gov (indexed) [DOE]

    Exclusion Determination CX-011544: Categorical Exclusion Determination Innovative Elution Processes for Recovering Uranium and Transition Metals from Amidoxime-based Sorbents CX(s)...

  4. EC RESEARCH AND DEVELOPMENT REPORT .:'

    Office of Legacy Management (LM)

    removed from the resin by continuous countercurrent elution either in a column or tanks. Uranium reduction processes employing sodium amalgam and hydrogen were studied in the...

  5. Technetium-99m generator system

    DOE Patents [OSTI]

    Mirzadeh, Saed (Knoxville, TN); Knapp, Jr., Furn F. (Oak Ridge, TN); Collins, Emory D. (Knoxville, TN)

    1998-01-01T23:59:59.000Z

    A .sup.99 Mo/.sup.99m Tc generator system includes a sorbent column loaded with a composition containing .sup.99 Mo. The sorbent column has an effluent end in fluid communication with an anion-exchange column for concentrating .sup.99m Tc eluted from the sorbent column. A method of preparing a concentrated solution of .sup.99m Tc includes the general steps of: a. providing a sorbent column loaded with a composition containing .sup.99 Mo, the sorbent column having an effluent end in fluid communication with an anion-exchange column; b. eluting the sorbent column with a salt solution to elute .sup.99m Tc from the sorbent and to trap and concentrate the eluted .sup.99m Tc on the ion-exchange column; and c. eluting the concentrated .sup.99m Tc from the ion-exchange column with a solution comprising a reductive complexing agent.

  6. Technetium-99m generator system

    DOE Patents [OSTI]

    Mirzadeh, S.; Knapp, F.F. Jr.; Collins, E.D.

    1998-06-30T23:59:59.000Z

    A {sup 99}Mo/{sup 99m}Tc generator system includes a sorbent column loaded with a composition containing {sup 99}Mo. The sorbent column has an effluent end in fluid communication with an anion-exchange column for concentrating {sup 99m}Tc eluted from the sorbent column. A method of preparing a concentrated solution of {sup 99m}Tc includes the general steps of: (a) providing a sorbent column loaded with a composition containing {sup 99}Mo, the sorbent column having an effluent end in fluid communication with an anion-exchange column; (b) eluting the sorbent column with a salt solution to elute {sup 99m}Tc from the sorbent and to trap and concentrate the eluted {sup 99m}Tc on the ion-exchange column; and (c) eluting the concentrated {sup 99m}Tc from the ion-exchange column with a solution comprising a reductive complexing agent. 1 fig.

  7. The use of solvent extraction in trace metal analysis by atomic absorption spectroscopy

    E-Print Network [OSTI]

    Eddy, Raymond Douglas

    1968-01-01T23:59:59.000Z

    . , reagen4 grade. NamHPOn ~ 7H-. . G T ' Till 68 08 Fe . ?. 0. 0003'Ii. S~ diun; di. hy;!i'cg=n phosphate, J. T. Baker, rcag?nt grade. F. W. 138. 00. Sodium tartrate, J. T. Baker, reagent grade. Nae04H40e 2HnO F. W. 250. 08 Fe = 0. 0002/0. d... the sta!&dards ;&ere prepared. The solutions werc pipeti, ed. into a 125&-ml pear-sba d. separatory funnel and. 5 ml of 41 reagen4 sclurion &;as added. '!ne rsixture was shaken for I'ive s&inutes. 'The layers were allowed to separate snd th or- ganic...

  8. The use of the photo-electric cell in the determination of ammonia

    E-Print Network [OSTI]

    Adams, Leon Milton

    1934-01-01T23:59:59.000Z

    of the "~'1oulturul end )%~oh". uicul Callo' of' Tox~s ; ertial !"ulflltw. nt of the Bequixc-:. onto for the De8roe of UGotor of' . ' ogsnco ;, eJor "ub$oot: 83r Leon ffilto~ Adam xupgct l9, 4 Cia']KENT ' 91CWQQ i i X ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ e ~ ~ I...~i~ated by tho substitution of th&: c. ll since its rco. xnsc to a &', ivan dap'h of color is a" a'"a the oa m hi, p de, ~ee Of ac~ay in rocp~nae hae bosn prOVen by artridgo in '. io . cork in precise titranetry. Pe obtained results hich checked each o'~', er...

  9. E-Print Network 3.0 - americium oxides Sample Search Results

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Recovery and Uses of Americium... generator. The generator technology immobilizes the strontium-82 on a metal-oxide support allowing elution... on the basis of titanium(IV) oxide...

  10. Septin Self-Assembly: Plasticity and Protein Scaffolding

    E-Print Network [OSTI]

    Garcia, III, Galo

    2012-01-01T23:59:59.000Z

    column (HisTrap HP, General Electric Healthcare) at 2 ml/120 ml column volume, General Electric Healthcare) for size-1ml Resource Q column, General Electric Healthcare. To elute

  11. GE Healthcare Data File 11-0036-90 AA GraviTrap column

    E-Print Network [OSTI]

    Lebendiker, Mario

    and elution (Fig 1). One purification run takes approximately 30 minutes (depending on sample volume phosphate buffer concentrates and highly pure 2 M imidazole stock solutions, thus eliminating time

  12. E-Print Network 3.0 - alpha subunit peptide Sample Search Results

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    -terminal beta-barrel domain of the alpha and beta subunits in the yeast F1-ATPase. J Bioenerg Biomembr 1999... stained bands (Fig. 1A) were eluted, digested with trypsin, and ......

  13. New tools for target identification by affinity chromatography

    E-Print Network [OSTI]

    Landi, Felicetta

    2011-06-27T23:59:59.000Z

    The recovery of the selected biological material in affinity-based separations relies on reversing the biological interaction responsible for the binding. General elution methods which are independent of the bioaffinity ...

  14. Luminal flow amplifies stent-based drug deposition in arterial

    E-Print Network [OSTI]

    Levine, Evan G.

    Background: Treatment of arterial bifurcation lesions using drug-eluting stents (DES) is now common clinical practice and yet the mechanisms governing drug distribution in these complex morphologies are incompletely ...

  15. Specific and general binding in arterial drug delivery

    E-Print Network [OSTI]

    Levin, Andrew D. (Andrew David), 1976-

    2005-01-01T23:59:59.000Z

    Drug-eluting stents have emerged as the most effective method for treating restenosis following percutaneous coronary interventions. This thesis investigates how drugs with similar physiochemical properties but different ...

  16. Drug deposition and distribution in healthy and atherosclerotic arteries and in models of atherosclerosis following bulk or stent-based drug delivery

    E-Print Network [OSTI]

    Vukmirovic, Neda

    2007-01-01T23:59:59.000Z

    Drug eluting stents have revolutionized the practice of medicine and the landscape of medical devices. Yet, more than four years after introduction clinical trial data and clinical use have still not fully clarified what ...

  17. Stent Thrombogenicity Early in High Risk Interventional Settings is Driven by Stent Design and Deployment, and Protected by Polymer-Drug Coatings

    E-Print Network [OSTI]

    Kolandaivelu, Kumaran

    BackgroundStent thrombosis is a lethal complication of endovascular intervention. Concern has been raised about the inherent risk associated with specific stent designs and drug-eluting coatings, yet clinical and animal ...

  18. Development of an Automatic Method for Americium and Plutonium Separation and

    E-Print Network [OSTI]

    Sánchez, David

    Development of an Automatic Method for Americium and Plutonium Separation and Preconcentration and separation in a short time using large sample volumes. Americium is eluted from the column with 4 mol L-1

  19. Computational model of local intravascular drug delivery

    E-Print Network [OSTI]

    Balakrishnan, Brinda

    2007-01-01T23:59:59.000Z

    Drug-eluting stents (DES) virtually eradicate the clinical phenomena of vessel restenosis; yet, they also increase the short and long term risks for stent thrombosis. To improve their safety and efficacy, it is critical ...

  20. Kava Components Down-Regulate Expression of AR and AR Splice Variants and Reduce Growth in Patient-Derived Prostate Cancer Xenografts in Mice

    E-Print Network [OSTI]

    2012-01-01T23:59:59.000Z

    elution: (A) Water: Acetonitrile: acetic acid (97.8:2:0.2v/v/v), and (B) Acetonitrile: acetic acid 99.8:0.2 (v/v) as

  1. E-Print Network 3.0 - alpha-spectrometry vliyanie toriya Sample...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    by activity determination using combinations of LSC, alpha spectrometry or ICP-MS. Uranium... Extraction with TBP from 8 M HNO3, rinse with 1.2 M HCl and elution with water...

  2. Modeling the behavior of Cm and Am during separation by complexing extraction chromatography

    SciTech Connect (OSTI)

    Chuveleva, E.A.; Kharitonov, O.V.; Firsova, L.A.

    1994-11-01T23:59:59.000Z

    Certain heavy rare earths (REE), Cm, and Am are separated by complexing extraction chromatography using solutions of DTPA and DTPA-citric acid as eluents. The separation coefficients of REE from Cm and Am are calculated. Tracers are proposed for the Cm and Am separations. These are Tm for Cm elution using 0.025 M DTPA and Ho for Cm elution using 0.025 M DTPA with 0.025 citric acid. The tracer for Am in both instances is Tb.

  3. Escherichia coli proteomics and bioinformatics

    E-Print Network [OSTI]

    Niu, Lili

    2009-05-15T23:59:59.000Z

    ???? ...????????..?????. .?.. 25 2.7 Comparisons of the distributions of molecular weight (A) and pI (B) between heparin-binding proteins and predicted proteins of the whole genome? .? ????????????????? ..? .??.?. ... 26 2.8 Functional... Page 2.12 pI distribution of heparin-binding proteins in elution fractions of the exponential growth sample...?????.? ??...??????.?.. 38 2.13 pI distribution of heparin-binding proteins in elution fractions...

  4. Garg, Sarpong, and Stoltz: Dragmacidin D Synthesis 1 Supplemental materials for

    E-Print Network [OSTI]

    Stoltz, Brian M.

    a Rainin C18, Microsorb MV, 5mm, 300 x 4.6 mm reversed-phased column in 0.1% (wt/v) TFA with acetonitrile as eluent and a flow rate of 1.0 mL/min, gradient elution of 1.25% acetonitrile/min. Preparatory reversed with a guard, 0.1% (wt/v) TFA with acetonitrile as eluent, and gradient elution of 0.50% acetonitrile

  5. www.sciencemag.org/cgi/content/full/315/5810/513/DC1 Supporting Online Material for

    E-Print Network [OSTI]

    Bruns, Tom

    .5% ethanol and passed through a column packed with approximately 100 mg of CF11 cellulose using a slow speedCl, 50 mM Tris pH 8, 0.5 mM EDTA pH 8, 16.5 % ethanol). The dsRNA was eluted in 4.5 ml of elution buffer) and precipitated at -20°C overnight with 10 ml of ice cold absolute ethanol (100%). After centrifugation, pellets

  6. Isolation and purification of a bovine milk lipase

    E-Print Network [OSTI]

    Alford, Edna Sustek

    1979-01-01T23:59:59.000Z

    ISOLATION AND PURIFICATION OF A BOVINE MILK LIPASE A Thesis by EDNA SUSTEK ALFORD Approved to style an cpntent by: / / (Chairman of C mmittee) Head of Depa ment) (Member7) (Member) December 1979 ABSTRACT Isolation and Purification of a.... Elution profile of the sodium taurocholate treated fraction on Sephadex G-50. The arrows denote the fractions collected for additional purification. 17 3. Elution profile of the electrofocused lipolytic fraction ( ? ) superimposed over the pH gradient...

  7. Relation of Soil Nitrogen, Nitrification and Ammonification to Pot Experiments.

    E-Print Network [OSTI]

    Fraps, G. S. (George Stronach)

    1921-01-01T23:59:59.000Z

    ............................................ 6 Relation of the Crops to the Total Nitrogen of the Soil ........... 7 Relation of the Different Crops ................................. 8 Relation of Surface Soil to Subsoil ............................. 13 Acid Soils Compared with Non-Acid... of Production of Nitrates to the Results of the Pot Ex- periments ................................................ 21 Extensive Work ............................................ 24 Relation of Nitric Nitrogen to Nitrogen Removed by First Crop .... 24...

  8. Breaking the Fuel Cell Cost Barrier AMFC Workshop

    E-Print Network [OSTI]

    (PFM-FC) 5 Light metal hardware Non-acidic membrane Non- platinum catalysts 70% cost savings and above batteries and diesel generators #12;PFM vs. PEM stack- Cost Analysis per kW at 10^3 unit volumes 6 PFM upgraded for stack level fabrication and testing 7 #12;Cellera's AMFC : Hydrogen/Air, 2/2 bar, 80 deg C

  9. Method and system for radioisotope generation

    DOE Patents [OSTI]

    Toth, James J.; Soderquist, Chuck Z.; Greenwood, Lawrence R.; Mattigod, Shas V.; Fryxell, Glen E.; O'Hara, Matthew J.

    2014-07-15T23:59:59.000Z

    A system and a process for producing selected isotopic daughter products from parent materials characterized by the steps of loading the parent material upon a sorbent having a functional group configured to selectively bind the parent material under designated conditions, generating the selected isotopic daughter products, and eluting said selected isotopic daughter products from the sorbent. In one embodiment, the process also includes the step of passing an eluent formed by the elution step through a second sorbent material that is configured to remove a preselected material from said eluent. In some applications a passage of the material through a third sorbent material after passage through the second sorbent material is also performed.

  10. Comprehensive off-line, two-dimensional liquid chromotography. Application to the separation of peptide digest

    SciTech Connect (OSTI)

    Marchetti, Nicola [University of Tennessee, Knoxville (UTK); Guiochon, Georges A [ORNL

    2008-01-01T23:59:59.000Z

    The separation of the peptide digests of myoglobin and bovine serum albumin was performed with an off-line combination of two commercial, conventional HPLC columns. The first column was packed with a strong ion exchanger and eluted with a KCl gradient. The second column was packed with particles of C{sub 18}-bonded silica and eluted with an acetonitrile gradient. The conditional peak capacities of the 2D separations achieved exceed 7000 under the experimental conditions investigated. This performance is achieved at the cost of an analysis time of the order of 28 hours. Possible improvements to the separation method described here are discussed.

  11. Random solutions of random problems...are not just random

    E-Print Network [OSTI]

    Achlioptas, Dimitris

    2008-01-01T23:59:59.000Z

    Let I(n,m) denote a uniformly random instance of some constraint satisfaction problem CSP with n variables and m constraints. Assume that the density r=m/n is small enough so that with high probability I(n,m) has a solution, and consider the experiment of first choosing an instance I=I(n,m) at random, and then sampling a random solution sigma of I (if one exists). For many CSPs (e.g., k-SAT, k-NAE, or k-coloring), this experiment appears difficult both to implement and to analyze; in fact, for a large range of r, no efficient algorithm is known to even compute a single solution of I. In the present paper we show that for many CSPs the above experiment is essentially equivalent to first choosing a random assignment sigma to the n variables, and then drawing a random instance satisfied by sigma uniformly. In general, this second experiment is very easy to implement and amenable to a rigorous analysis. In fact, using this equivalence, we can analyze the solution space of random CSPs. Thus, we can achieve the lon...

  12. Measurement of lithium isotope ratios by quadrupole-ICP-MS: application to seawater and natural carbonates

    E-Print Network [OSTI]

    Weston, Ken

    Measurement of lithium isotope ratios by quadrupole-ICP-MS: application to seawater and natural method for lithium isotope ratio (7 Li/6 Li) determinations with low total lithium consumption ( lithium from all matrix elements using small volume resin (2 ml/3.4 meq AG 50W-X8) and low volume elution

  13. W W W . Q I A G E N . C O M QproteomeTM

    E-Print Network [OSTI]

    Lebendiker, Mario

    Contents 4 Storage 4 Quality Control 4 Safety Information 5 Product Warranty and Satisfaction Guarantee 6. Elution Buffer should be stored at ­20°C after reconstitution. Quality Control In accordance with QIAGEN's ISO-certified Total Quality Management System, Qproteome Kits are tested against predetermined

  14. W W W . Q I A G E N . C O M QproteomeTM

    E-Print Network [OSTI]

    Lebendiker, Mario

    Product Use Limitations 4 Quality Control 4 Product Warranty and Satisfaction Guarantee 5 Technical in the handling of many of the materials described in this text. Quality Control In accordance with QIAGEN's ISO-certified Total Quality Management System, each lot of QIAamp MinElute Media Kit is tested against predetermined

  15. n engl j med 367;25 nejm.org december 20, 2012 2375 The new england

    E-Print Network [OSTI]

    Paris-Sud XI, Université de

    for patients with diabetes, coronary-artery bypass grafting (CABG) has had a better outcome than percutaneous coronary intervention (PCI). We sought to discover whether aggres- sive medical therapy and the use of drug-eluting stents could alter the revascular- ization approach for patients with diabetes and multivessel coronary

  16. Basic Science Effects of Curcumin for Preventing Restenosis in a

    E-Print Network [OSTI]

    Park, Jong-Sang

    in percutaneous coronary interven- tions (PCIs). Unfortunately, in-stent restenosis triggered by metal-eluting stent; restenosis INTRODUCTION Coronary artery narrowing caused by atherosclerosis is treated routinely by percutaneous transluminal coro- nary angioplasty (PTCA); however, restenosis, a seri- ous complication

  17. MATHEMATICAL BIOSCIENCES doi:10.3934/mbe.2009.6.493 AND ENGINEERING

    E-Print Network [OSTI]

    Pontrelli, Giuseppe

    . Percutaneous transluminal angioplasty has been used in the past to treat coronary occlusion (stenosis) due. Olufsen) Abstract. Implantation of drug eluting stents following percutaneous trans- luminal angioplasty observed after intervention [2] indicated the requirement of alternative approaches. The use of bare

  18. Southern Blotting Assemble the LKB Vacugene vacuum blotting unit on a leveling table. Place the white plastic backing

    E-Print Network [OSTI]

    Shoubridge, Eric

    the plastic mask. Ensure that there are no air bubbles or dirt under the membrane. After electrophoresis photograph the gel on the UV transilluminator. Note: For a southern blot to detect mtDNA deletions UVL tube. This fraction contains the purified probe. Pipet 4L (1 /100 of the elution volume

  19. Supplemental Material for Jiang et al, Tumor Imaging via Proteolytic Activation of Cell Penetrating Peptides

    E-Print Network [OSTI]

    Tsien, Roger Y.

    and vigorously stirred in air for 3 hr. The crude cyclic peptide was purified on HPLC (C18 reverse phase column purified on HPLC (C18 reverse phase column, eluted with 10-40% acetonitrile in water with 0.1% CF3COOH, and the concentration of each peptide stock solution was verified by UV- vis absorbance. Peptide disulfide bond

  20. Supporting Information for Cribrostatin 6 induces death in cancer cells through a reactive

    E-Print Network [OSTI]

    Hergenrother, Paul J.

    Procedures All reactions were conducted in oven-dried glassware when appropriate and air- or water- sensitive were visualized by UV light (254 or 365 nm). 1 H NMR spectra and 13 C NMR spectra were recorded. The crude material was purified via silica gel column chromatography eluting with 1:1 ethyl acetate

  1. Supplemental Data Directed Evolution of ATP Binding Proteins

    E-Print Network [OSTI]

    Heller, Eric

    Supplemental Data Directed Evolution of ATP Binding Proteins from a Zinc Finger Domain Using m TG 3'). Denaturing Ni-NTA was performed on the ATP-column elution for round 2, and then FLAG with the resin, but instead passed directly over the immobilized ATP. The selection was performed at room

  2. Nature Macmillan Publishers Ltd 1998 letters to nature

    E-Print Network [OSTI]

    Hansell, Dennis

    was excised (Fig. 2c), and RNA was eluted in 300 mM NaCl, 20 mM DTT, then precipitated with ethanol. After; RNAwas then twice precipitated with ethanol to remove excess biotin. About 75% of material end- mide gel and precipitated with ethanol. Uracil counts associated with the RNA were determined

  3. Calcite dissolution and Ca/Na ion-exchange reactions in columns with different flow rates through high ESR soil

    E-Print Network [OSTI]

    Navarre, Audrey

    1999-01-01T23:59:59.000Z

    min? under conditions of saturated flow. Column eluate was monitored for pH, carbonate alkalinity, and Na, Ca and Cl concentrations to evaluate the elution of SAR 10 solution, dissolution of CaCO? and exchange of Na by Ca on the cation...

  4. Preliminary Ion Exchange Modeling for Removal of Cesium from Hanford Waste Using SuperLig 644 Resin

    SciTech Connect (OSTI)

    Hamm, L.L.

    2000-08-23T23:59:59.000Z

    A proposed facility is being designed for the immobilization of Hanford high-level radioactive waste. One unit process in the facility is designed to remove radioactive cesium by ion-exchange from the strongly alkaline aqueous phase. A resin specifically designed with high selectivity of cesium under alkaline conditions is being investigated. The resin also is elutable under more acidic conditions. The proposed design of the facility consists of two sets of two packed columns placed in series (i.e., a lead column followed by a lag (guard) column configuration). During operation, upon reaching a specified cesium concentration criterion at the exit of the lag column, operation is switched to the second set of lead and lag columns. The cesium-loaded lead column is processed (i.e., washed and eluted) and switched to the lag position. the previous lag column is then placed in the lead position (without eluting) and the system is ready for use in the next cycle. For a well designed process, the loading and elution processes result in significant volume reductions in aqueous high-level waste.

  5. trends inI?nalytical chemistry, vol. 4, no. 3,X985 75 Analytical applications of ultraviolet

    E-Print Network [OSTI]

    Asher, Sanford A.

    - nique to studies of polycyclic aromatic hydrocarbons (PAHs) in coat liquids and in tissue. UVRR can also be used to speci- ate PAHs eluting from high-pe$ormance liquid chromato- graphy columns. Other, detection and identification of environmental pollu- tants, pesticide research, and coal and petroleum re

  6. B American Society for Mass Spectrometry, 2012 DOI: 10.1007/s13361-012-0404-0

    E-Print Network [OSTI]

    Komives, Elizabeth A.

    pI, mobile phase pH) [12], ion suppression of co-eluting analytes [13], and mobile phase flow rateB American Society for Mass Spectrometry, 2012 DOI: 10.1007/s13361-012-0404-0 J. Am. Soc. Mass Improves Peptide Identification by Tandem Mass Spectrometry Jesse G. Meyer, Elizabeth A. Komives Department

  7. Osmium-191/iridium-191m radionuclide

    DOE Patents [OSTI]

    Knapp, F.F. Jr.; Butler, T.A.; Brihaye, C.

    1985-08-26T23:59:59.000Z

    A generator system to provide iridium-191m for clinical imaging applications comprises an activated carbon adsorbent loaded with a compound containing the parent nuclide, osmium-191. The generator, which has a shelf-life in excess of two weeks and does not require a scavenger column, can be eluted with physiologically compatible saline. 4 figs. 3 tabs.

  8. Supplementary Information Primary amines protect against retinal degeneration in

    E-Print Network [OSTI]

    Palczewski, Krzysztof

    µm column, linear gradient of acetonitrile in water (0­ 100% acetonitrile over 20 min at a flow rate) in a linear gradient of acetonitrile in water (80 ­ 100% acetonitrile over 20 min at a flow rate of 1.5 ml/min). Both solvents contained 0.05% trifluoroacetic acid (TFA). HPLC elution: 9.0 min. UV/Vis (acetonitrile

  9. Supplemental Experimental Procedures Cell Culture and Induction of Apoptosis

    E-Print Network [OSTI]

    Cravatt, Benjamin

    and acetonitrile. The pooled supernatant was dried and resuspended in 10 µl buffer A (95% H2O, 5% acetonitrile, 0 eluted from the column using a 2-hour gradient of 5-100% Buffer B (Buffer B: 20% H2O, 80% acetonitrile, 0

  10. STAGE (STop And Go Extraction) TIPS Clean up Procedure: Detergent and Salt Removal "MCX-like method"

    E-Print Network [OSTI]

    Weiblen, George D

    pH 3 b) Ensure that organic (acetonitrile, methanol) concentration is at or below 5 ­ 10% c) Adjust Conditioning solvent A: acetonitrile Conditioning solvent B: ultrapure water Wash solvent A: 95:5:0.2%, water : acetonitrile : formic acid (FA) Wash solvent B: acetonitrile Elution solvent: 60:35:5%, acetonitrile : water

  11. Cell Stem Cell, Volume 5 Supplemental Data

    E-Print Network [OSTI]

    .1% formic acid. Peptides were eluted with 40 l 80% acetonitrile, 0.1% formic acid. The eluate was dried completely and subsequently reconstituted in 10 l 20% acetonitrile, 0.05% formic acid. #12;Strong Cation, Japan). After injection, the first 5 min were ran isocratic at 100% solvent A (20% acetonitrile, 0

  12. GE Healthcare Instructions 28-9367-25 AA Affinity media

    E-Print Network [OSTI]

    Lebendiker, Mario

    (II)-tagged proteins. Purification is done under physiological conditions and mild elution preserves the activity...................................................................................8 5. Scale up................................................................................... 11 This robust, high-resolution medium is based on the 34 m Sepharose High Performance matrix. Due to the small

  13. Nitrification in Texas Soils.

    E-Print Network [OSTI]

    Fraps, G. S. (George Stronach)

    1920-01-01T23:59:59.000Z

    have a high nitrificati is the balmcing of these extremes which redlices the average le between acid ancl non-acid soils. C03TPOSITION OF SOILS TVITFI LOW AND HIGH NITRIFIC-4TION. Table 11 contains the chemical composition of soils having low nitl... are subsoils. Subsoils thus possess nnu~nally high and unusually low nitrification. Table 11.-Chemical composition of soils with nitrification below 10 . I Average .............................. Nitri- fication 7164 7090 4596' 5710 4645 3976 3657 3...

  14. Migration in alluvium of chlorine-36 and tritium from an underground nuclear test

    SciTech Connect (OSTI)

    Ogard, A.E.; Thompson, J.L.; Rundberg, R.S.; Wolfsberg, K.; Kubik, P.W.; Elmore, D.; Bentley, H.W.

    1987-01-01T23:59:59.000Z

    This article describes a field experiment studying the migration in alluvium of radioactive elements away from an underground nuclear explosion at the Nevada Test Site in the United States. Nuclides detected in the pumped water are tritium, chlorine-36, iodine-129, and krypton-85 - all at levels below the maximum permissible concentration for drinking water in controlled areas. The chlorine-36 elution curve precedes that of tritium, and is due to an anion exclusion process. A conventional two-dimensional convection-diffusion equation does not fully describe the elution curves for tritium and chlorine-36; the tailing of the curves is longer than predicted. Successful modeling of this experiment will be important for validating codes and models to be used in the high-level nuclear waste program.

  15. Size-exclusion chromatography system for macromolecular interaction analysis

    DOE Patents [OSTI]

    Stevens, Fred J. (Downers Grove, IL)

    1988-01-01T23:59:59.000Z

    A low pressure, microcomputer controlled system employing high performance liquid chromatography (HPLC) allows for precise analysis of the interaction of two reversibly associating macromolecules such as proteins. Since a macromolecular complex migrates faster than its components during size-exclusion chromatography, the difference between the elution profile of a mixture of two macromolecules and the summation of the elution profiles of the two components provides a quantifiable indication of the degree of molecular interaction. This delta profile is used to qualitatively reveal the presence or absence of significant interaction or to rank the relative degree of interaction in comparing samples and, in combination with a computer simulation, is further used to quantify the magnitude of the interaction in an arrangement wherein a microcomputer is coupled to analytical instrumentation in a novel manner.

  16. Size exclusion chromatography-inductively coupled plasma atomic emission spectrographic study of Fe in bitumens derived from tar sands

    SciTech Connect (OSTI)

    Reynolds, J.G. (Lawrence Livermore National Lab., Livermore, CA (US)); Biggs, W.R. (Chevron Research Co., Richmond, CA (US))

    1992-01-01T23:59:59.000Z

    This paper reports on bitumens extracted from tar sands from various locations (Utah, California, Kentucky, and Alberta) that were examined by size exclusion chromatography with on-line element-specific detection to study the Fe concentration as a function of size. In most cases, the resulting profiles exhibit unimodal distributions at relatively large molecular size with very similar times for maximum elution. specifically, Sunnyside (Utah) and McKittrick (California) tar-sand bitumens exhibited very intense maxima consistent with extremely high bulk Fe contents. Arroyo Grande (California) exhibited an additional maximum at very large molecular size. This size behavior of the Fe appears to correlate with the large molecular size Ni and V components eluted under the same conditions.

  17. High Throughput Identification, Purification and Structural Characterization of Water Soluble Protein Complexes in Desulfovibrio vulgaris

    SciTech Connect (OSTI)

    Dong,, Ming; Han, Bong-Gyoon; Liu, Hui-Hai; Malik, J.; Geller, Jil; Yang, Li; Choi, M.; Chandonia, John-Marc; Arbelaez, Pablo; Sterling, H. J.; Typke, Dieter; Shatsky, Max; Brenner, Steve; Fisher, Susan; Williams, Evan; Szakal, Evelin; Allen, S.; Hall, S. C.; Hazen, Terry; Witkowska, H. E.; Jin, Jiming; Glaeser, Robert; Biggin, Mark

    2010-05-17T23:59:59.000Z

    Our scheme for the tagless purification of water soluble complexes. 10 g of protein from a crude bacterial extract is first fractionated by ammonium sulfate precipitation and then by a series of chromatographic steps: anion exchange (IEX), hydrophobic interaction (HIC), and finally size exclusion (Gel Filtration). Fractions from the last chromatography step are trypsin digested and peptides labeled with iTRAQ reagents to allow multiplexing and quantitation during mass spectrometric analysis. Elution profiles of identified proteins are then subjected to clustering analysis.

  18. Method for liquid chromatographic extraction of strontium from acid solutions

    DOE Patents [OSTI]

    Horwitz, E. Philip (Naperville, IL); Dietz, Mark L. (Evanston, IL)

    1992-01-01T23:59:59.000Z

    A method and apparatus for extracting strontium and technetium values from biological, industrial and environmental sample solutions using a chromatographic column is described. An extractant medium for the column is prepared by generating a solution of a diluent containing a Crown ether and dispersing the solution on a resin substrate material. The sample solution is highly acidic and is introduced directed to the chromatographic column and strontium or technetium is eluted using deionized water.

  19. Liquid chromatographic extraction medium

    DOE Patents [OSTI]

    Horwitz, E. Philip (Naperville, IL); Dietz, Mark L. (Evanston, IL)

    1994-01-01T23:59:59.000Z

    A method and apparatus for extracting strontium and technetium values from biological, industrial and environmental sample solutions using a chromatographic column is described. An extractant medium for the column is prepared by generating a solution of a diluent containing a Crown ether and dispersing the solution on a resin substrate material. The sample solution is highly acidic and is introduced directed to the chromatographic column and strontium or technetium is eluted using deionized water.

  20. Method for aqueous gold thiosulfate extraction using copper-cyanide pretreated carbon adsorption

    DOE Patents [OSTI]

    Young, Courtney; Melashvili, Mariam; Gow, Nicholas V

    2013-08-06T23:59:59.000Z

    A gold thiosulfate leaching process uses carbon to remove gold from the leach liquor. The activated carbon is pretreated with copper cyanide. A copper (on the carbon) to gold (in solution) ratio of at least 1.5 optimizes gold recovery from solution. To recover the gold from the carbon, conventional elution technology works but is dependent on the copper to gold ratio on the carbon.

  1. Liquid chromatographic extraction medium

    DOE Patents [OSTI]

    Horwitz, E.P.; Dietz, M.L.

    1994-09-13T23:59:59.000Z

    A method and apparatus are disclosed for extracting strontium and technetium values from biological, industrial and environmental sample solutions using a chromatographic column. An extractant medium for the column is prepared by generating a solution of a diluent containing a Crown ether and dispersing the solution on a resin substrate material. The sample solution is highly acidic and is introduced directed to the chromatographic column and strontium or technetium is eluted using deionized water. 1 fig.

  2. Elisabethamine: a new diterpene alkaloid from Pseudopterogorgia elisabethae

    E-Print Network [OSTI]

    Kerr, Russell G.

    chromatography using silica gel as adsorbent and hexane±ethyl acetate (0±100%) and ethyl acetate±methanol (0±100%) as eluents. The fraction obtained on elution with 80% ethyl acetate/20% hexane was subjected to reverse phase groups, respectively. Two three-proton singlets at 1.66 and 1.80 were assigned to the allylic C-16 and C

  3. Ion exchange selectivity of a perfluorosulfonate ionomer

    E-Print Network [OSTI]

    Wilkerson, James Edward

    1983-01-01T23:59:59.000Z

    of Advisory Committee: Dr. C. R. Martin The ion exchange selectivity of Nafion was evaluated. Two separate series of homologous cations were separated. A series of viologens, methyl, benzyl, and heptyl, were sepa- rated by utilizing tetramethyl ammonium... which demonstrated X m the ionic exchange characteristic of the system. Comparison of the elution volumes of methyl viologen on ODS (1. 80 ml) and on Nafion coated ODS (9. 50 ml) also indicates the ionic characteristic of the Nafion column...

  4. Qualitative and quantitative analysis of low molecular weight phenols by high pressure liquid chromatography

    E-Print Network [OSTI]

    Hahn, David Henry

    2012-06-07T23:59:59.000Z

    . A. , Bethany College Chairman of Advisory Comnittee: Dr. Lloyd W. Rooney A high performance liquid chromatographic (HPI C) method was de- veloped for the separation and identification of substituted benzoic and cinnamic acids (phenolic acids...). The 8 commonly occurring phenolic acids chosen as standards were: gallic, protocatechuic, p-hydroxyben- zoic, vanillic, caffeic, p-coumaric, feruli c and ci nnami c acids. Separation was on a nonpolar C18 substituted, silica based column with elution...

  5. Size exclusion chromatography for the unambiguous detection of aliphatics in fractions from petroleum vacuum residues, coal liquids, and standard materials, in the presence of aromatics

    SciTech Connect (OSTI)

    Eiman M. Al-Muhareb; Fatma Karaca; Trevor J. Morgan; Alan A. Herod; Ian D. Bull; Rafael Kandiyoti [Imperial College, London (United Kingdom). Department of Chemical Engineering

    2006-05-15T23:59:59.000Z

    A method has been developed using size exclusion chromatography (SEC) in heptane eluent that can detect aliphatics unambiguously without fractionation to remove aromatics. Spherical molecules such as colloidal silicas elute at the exclusion limit, while alkanes up to C{sub 50} elute through the porosity of the column. Detection of aliphatics was defined by use of an evaporative light scattering (ELS) detector with the simultaneous absence of UV absorbance at 300 nm. Alkanes smaller than C{sub 12} were not detected because the conditions of operation of the ELS caused their evaporation. All aromatics eluted after the permeation limit of about 25 min and were not detected until well after 45 min by their UV absorbance. The SEC method was applied to petroleum vacuum residues and coal liquids, and their fractions were soluble in pentane or heptane. High-temperature (HT) GC-MS confirmed the presence of alkanes in the pentane- and heptane-soluble fractions of petroleum vacuum residues, but did not elute any of the aromatics known to be present from SEC. Alkanes were examined in pentane-soluble fractions of a coal digest and a low-temperature coal tar; alkanes up to C{sub 40} were detected in the low-temperature tar and, although present in the digest, were masked by aromatics. No alkanes were detected by either SEC or HT GC-MS in fractions from a coal tar pitch. Aromatics in coal liquids and one petroleum residue were also examined by SEC using NMP as eluent and by UV fluorescence spectroscopy. The SEC method will find application to pentane- and heptane-soluble fractions of petroleum liquids and coal liquids where the alkanes are concentrated relative to the more abundant aromatics. 43 refs., 10 figs., 2 tabs.

  6. Radiopharmaceutical composition containing tantalum-178 and process therefor

    DOE Patents [OSTI]

    Neirinckx, Rudi D. (Medfield, MA); Holman, B. Leonard (Chestnut Hill, MA); Davis, Michael A. (Westwood, MA); Harris, Gale I. (East Lansing, MI)

    1989-05-16T23:59:59.000Z

    A physiologically acceptable solution of tantalum-178 having an activity of 0.1 to 200 millicuries per milliliter of tantalum-178 solution is provided. The solution is obtained from tungsten-178 bound to a column of an anion exchange resin which forms tantalum-178 in situ by eluting the column with a hydrochloric acid solution containing hydrogen peroxide to form an acidic solution of tantalum-178. The acidic solution of tantalum-178 then is neutralized.

  7. Chromatographic extraction with di(2-ethylhexyl)orthophosphoric acid for production and purification of promethium-147

    DOE Patents [OSTI]

    Boll, Rose A [Knoxville, TN

    2008-10-14T23:59:59.000Z

    A method of producing and purifying promethium-147 including the steps of: irradiating a target material including neodymium-146 with neutrons to produce promethium-147 within the irradiated target material; dissolving the irradiated target material to form an acidic solution; loading the acidic solution onto a chromatographic separation apparatus containing HDEHP; and eluting the apparatus to chromatographically separate the promethium-147 from the neodymium-146.

  8. Garg, Caspi, and Stoltz: Dragmacidin F Supporting Information S1 Supporting Information for

    E-Print Network [OSTI]

    Stoltz, Brian M.

    .6 mm reversed-phased column in 0.1% (w/v) TFA with acetonitrile as eluent and a flow rate of 1.0 mL/min, gradient elution of 1.25% acetonitrile/min. Preparatory reversed-phase HPLC was performed on a Beckman HPLC with a Waters DeltaPak 25 x 100 mm, 100 µm C18 column equipped with a guard, 0.1% (w/v) TFA with acetonitrile

  9. Supplemental material JCB

    E-Print Network [OSTI]

    unknown authors

    anti-GFP antibody coupled to agarose, sepharose, or very small magnetic beads (QUBIC), digested on bead or in column with trypsin, and analyzed in a single run on the mass spectrometer. (right) In all three cases, the QUBIC purification was cleanest in terms of the smallest number of background proteins identified. QUBIC resulted in the best sequence coverage of the bait protein. (B) Different elution methods were tested on GFP-THOC3, including elution with SDS buffer followed by FASP (Wi?niewski et al., 2009), elution with 8 M urea, specific elution involving the PreScission cleavage site in the LAP tag, LysC in-column digest followed by trypsin digestion, and QUBIC (trypsin in-column digestion). (left) As expected, specific cleavage resulted in the highest purity of IP. (right) However, THOC3 is a typical example of a shielded PreScission cleavage site for the complexed bait, as most of the TREX components were not identified. The adequate coverage of the bait protein may result from purified free or UAP56-bound THOC3-GFP in the cell. Overall, QUBIC again resulted in the best sequence coverage of the bait protein. Quantitative BAC interactomics Hubner et al. S1 Figure S2. Additional SILAC pull-downs of the TREX complex components. (AE) Forward and reverse pull-down of THOC1, THOC3, THOC5, THOC7, and THOC4/Aly as described in Fig. 2. Specific interaction partners are annotated and marked with black dots. Proteins marked in red were not significant regarding their ratios. Bars, 10 m. S2 JCB Figure S3. Additional SILAC pull-down of CDC23. Single SILAC pull-down of CDC23 with double-SILAC labeling and tryptic digestion of proteins reveals all but one component of the APC and two new interactors, C10orf104/ANAPC16 and C11orf51, with P < 10 ?10.

  10. Method for the concentration and separation of actinides from biological and environmental samples

    DOE Patents [OSTI]

    Horwitz, E.P.; Dietz, M.L.

    1989-05-30T23:59:59.000Z

    A method and apparatus for the quantitative recover of actinide values from biological and environmental sample by passing appropriately prepared samples in a mineral acid solution through a separation column of a dialkyl(phenyl)-N,N-dialylcarbamoylmethylphosphine oxide dissolved in tri-n-butyl phosphate on an inert substrate which selectively extracts the actinide values. The actinide values can be eluted either as a group or individually and their presence quantitatively detected by alpha counting. 3 figs.

  11. Modeling Ion-Exchange Processing With Spherical Resins For Cesium Removal

    SciTech Connect (OSTI)

    Hang, T.; Nash, C. A.; Aleman, S. E.

    2012-09-19T23:59:59.000Z

    The spherical Resorcinol-Formaldehyde and hypothetical spherical SuperLig(r) 644 ion-exchange resins are evaluated for cesium removal from radioactive waste solutions. Modeling results show that spherical SuperLig(r) 644 reduces column cycling by 50% for high-potassium solutions. Spherical Resorcinol Formaldehyde performs equally well for the lowest-potassium wastes. Less cycling reduces nitric acid usage during resin elution and sodium addition during resin regeneration, therefore, significantly decreasing life-cycle operational costs. A model assessment of the mechanism behind ''cesium bleed'' is also conducted. When a resin bed is eluted, a relatively small amount of cesium remains within resin particles. Cesium can bleed into otherwise decontaminated product in the next loading cycle. The bleed mechanism is shown to be fully isotherm-controlled vs. mass transfer controlled. Knowledge of residual post-elution cesium level and resin isotherm can be utilized to predict rate of cesium bleed in a mostly non-loaded column. Overall, this work demonstrates the versatility of the ion-exchange modeling to study the effects of resin characteristics on processing cycles, rates, and cold chemical consumption. This evaluation justifies further development of a spherical form of the SL644 resin.

  12. Influence of the pressure on the properties of chromatographic columns I. Measurement of the compressibility of methanol-water mixtures on a mesoporous silica adsorbent

    SciTech Connect (OSTI)

    Gritti, Fabrice [University of Tennessee, Knoxville (UTK); Guiochon, Georges A [ORNL

    2005-03-01T23:59:59.000Z

    The compressibilities of aqueous solutions of methanol or acetonitrile containing 0, 20, 40, 60, 80 and 100% (v/v) organic solvent were measured with a dynamic chromatographic method. The elution volumes of thiourea samples (2 {micro} L) in these solutions were measured at different average column pressures, adjusted by placing suitable capillary restrictors on-line, after the detector. The reproducibility of the measurements was better than 0.2%. In the range of average pressures studied (10-350 bar), the maximum change in elution volume of thiourea is 1.3% (in pure water) and 4.0% (in pure methanol). This difference is due to the different compressibilities of these pure solvents. For mixtures, the plots of the elution volume of thiourea versus the pressure are convex downward, which is inconsistent with the opposite curvature predicted by the classical Tait model of liquid compressibility. This difference is explained by the variation of the amount of thiourea adsorbed with the pressure. The deconvolution of the two effects, adsorption of thiourea and solvent compressibility, allows a fair and consistent determination of the compressibilities of the methanol-water mixtures. A column packed with non-porous silica particles was also used to determine the compressibility of methanol-water and acetonitrile-water mixtures. A negative deviation by respect to ideal behavior was observed.

  13. Influence of the pressure on the properties of chromatographic columns I. Measurement of the compressibility of methanol-water mixtures on a mesoporous silica adsorbent

    SciTech Connect (OSTI)

    Gritti, Fabrice [University of Tennessee, Knoxville (UTK); Guiochon, Georges A [ORNL

    2005-04-01T23:59:59.000Z

    The compressibilities of aqueous solutions of methanol or acetonitrile containing 0, 20, 40, 60, 80 and 100% (v/v) organic solvent were measured with a dynamic chromatographic method. The elution volumes of thiourea samples (2 {micro} L) in these solutions were measured at different average column pressures, adjusted by placing suitable capillary restrictors on-line, after the detector. The reproducibility of the measurements was better than 0.2%. In the range of average pressures studied (10-350 bar), the maximum change in elution volume of thiourea is 1.3% (in pure water) and 4.0% (in pure methanol). This difference is due to the different compressibilities of these pure solvents. For mixtures, the plots of the elution volume of thiourea versus the pressure are convex downward, which is inconsistent with the opposite curvature predicted by the classical Tait model of liquid compressibility. This difference is explained by the variation of the amount of thiourea adsorbed with the pressure. The deconvolution of the two effects, adsorption of thiourea and solvent compressibility, allows a fair and consistent determination of the compressibilities of the methanol-water mixtures. A column packed with non-porous silica particles was also used to determine the compressibility of methanol-water and acetonitrile-water mixtures. A negative deviation by respect to ideal behavior was observed.

  14. Characterization and Application of Superlig 620 Solid Phase Extraction Resin for Automated Process Monitoring of 90Sr

    SciTech Connect (OSTI)

    Devol, Timothy A.; Clements, John P.; Farawila, Anne F.; O'Hara, Matthew J.; Egorov, Oleg; Grate, Jay W.

    2009-11-30T23:59:59.000Z

    Characterization of SuperLig 620 solid phase extraction resin was performed in order to develop an automated on-line process monitor for 90Sr. The main focus was on strontium separation from barium, with the goal of developing an automated separation process for 90Sr in high-level wastes. High-level waste contains significant 137Cs activity, of which 137mBa is of great concern as an interference to the quantification of strontium. In addition barium, yttrium and plutonium were studied as potential interferences to strontium uptake and detection. A number of complexants were studied in a series of batch Kd experiments, as SuperLig 620 was not previously known to elute strontium in typical mineral acids. The optimal separation was found using a 2M nitric acid load solution with a strontium elution step of ~0.49M ammonium citrate and a barium elution step of ~1.8M ammonium citrate. 90Sr quantification of Hanford high-level tank waste was performed on a sequential injection analysis microfluidics system coupled to a flow-cell detector. The results of the on-line procedure are compared to standard radiochemical techniques in this paper.

  15. Observation of time dependent dispersion in laboratory scale experiments with intact tuff

    SciTech Connect (OSTI)

    Rundberg, R.S.; Triay, I.R.; Ott, M.A.; Mitchell, A.J.

    1989-12-01T23:59:59.000Z

    The migration of radionuclides through intact tuff was studied using tuff from Yucca Mountain, Nevada. The tuff samples were both highly zeolitized ash-fall tuff from the Calico Hills and densely welded devitrified tuff from the Topopah Springs member of the Paintbrush tuff. Tritiated water and pertechnetate were used as conservative tracers. The sorbing tracers {sup 85}Sr, {sup 137}Cs, and {sup 133}Ba were used with the devitrified tuff only. Greater tailing in the elution curves of the densely welded tuff samples was observed that could be fit by adjusting the dispersion coefficient in the conventional Advection Dispersion Equation, ADE. The curves could be fit using time dependent dispersion as was previously observed for sediments and alluvium by Dieulin, Matheron, and de Marsily. The peak of strontium concentration was expected to arrive after 1.5 years based on the conventional ADE and assuming a linear K{sub d} of 26 ml/g. The observed elution had significant strontium in the first sample taken at 2 weeks after injection. The peak in the strontium elution occurred at 5 weeks. The correct arrival time for the strontium peak was achieved using a one dimensional analytic solution with time dependent dispersion. The dispersion coefficient as a function of time used to fit the conservative tracers was found to predict the peak arrival of the sorbing tracers. The K{sub d} used was the K{sub d} determined by the batch method on crushed tuff. 23 refs., 9 figs., 2 tabs.

  16. Improved resins and novel materials and methods for solid phase extraction and high performance liquid chromatography

    SciTech Connect (OSTI)

    Freeze, R.

    1997-10-08T23:59:59.000Z

    Solid-phase extraction (SPE) has grown to be one of the most widely used methods for isolation and preconcentration of a vast range of compounds from aqueous solutions. By modifying polymeric SPE resins with chelating functional groups, the selective uptake of metals was accomplished. The resin, along with adsorbed metals, was vaporized in the ICP and detection of the metals was then possible using either mass or emission spectroscopy. Drug analyses in biological fluids have received heightened attention as drug testing is on the increase both in sports and in the work environment. By using a direct-injection technique, biological fluids can be injected directly into the liquid chromatographic system with no pretreatment. A new surfactant, a sulfonated form of Brij-30 (Brij-S) is shown to prevent the uptake of serum proteins on commercial HPLC columns by forming a thin coating on the silica C18 surface. Excellent separations of eight or more drugs with a wide range of retention times were obtained. The separations had sharper peaks and lower retention times than similar separations performed with the surfactant sodium dodecylsulfate (SDS). Quantitative recovery of a number of drugs with limits of detection near 1 ppm with a 5 {micro}l injection volume were obtained. Finally, a method for solid-phase extraction in a syringe is introduced. The system greatly reduced the volume of solvent required to elute adsorbed analytes from the SPE bed while providing a semi-automated setup. SPE in a syringe consists of a very small bed of resin-loaded membrane packed into a GC or HPLC syringe. After extraction, elution was performed with just a few {micro}l of solvent. This small elution volume allowed injection of the eluent directly from the syringe into the chromatographic system, eliminating the handling problems associated with such small volumes.

  17. Gram-scale separation of curium from americium using alpha-hydroxyisobutyric acid in high-pressure cation columns

    SciTech Connect (OSTI)

    Bigelow, J.E.; Benker, D.E.; Chattin, F.R.; King, L.J.; Knauer, J.B.; Ross, R.G.; Stacy, R.G.; Wiggins, J.T.

    1984-01-01T23:59:59.000Z

    Quantities of heavy element (americium and curium) up to 2.3 g have been successfully separated by chromatographic elution from cation resin using alpha-hydroxyisobutyrate in equipment originally designed for decigram-scale separations of /sup 252/Cf and heavier elements. The high-pressure ion exchange process was reliable and relatively easy to operate. Overall curium recoveries of 80 to 90% were readily achieved with decontamination from americium by factors of 400 to 500. The product and waste streams are both in forms readily coupled to further processing steps.

  18. Tungsten-188/carrier-free rhenium-188 perrhenic acid generator system

    DOE Patents [OSTI]

    Knapp, Jr., Furn F. (Oak Ridge, TN); Lisic, Edward C. (Cookeville, TN); Mirzadeh, Saed (Knoxville, TN); Callahan, Alvin P. (Harriman, TN)

    1994-01-01T23:59:59.000Z

    A generator system for providing a carrier-free radioisotope in the form of an acid comprises a chromatography column in tandem fluid connection with an ion exchange column, the chromatography column containing a charge of a radioactive parent isotope. The chromatography column, charged with a parent isotope, is eluted with an alkali metal salt solution to generate the radioisotope in the form of an intermediate solution, which is passed through the ion-exchange column to convert the radioisotope to a carrier-free acid form.

  19. Tungsten-188/carrier-free rhenium-188 perrhenic acid generator system

    DOE Patents [OSTI]

    Knapp, Jr., Furn F. (Oak Ridge, TN); Lisic, Edward C. (Cookeville, TN); Mirzadeh, Saed (Knoxville, TN); Callahan, Alvin P. (Harriman, TN)

    1993-01-01T23:59:59.000Z

    A generator system for providing a carrier-free radioisotope in the form of an acid comprises a chromatography column in tandem fluid connection with an ion exchange column, the chromatography column containing a charge of a radioactive parent isotope. The chromatography column, charged with a parent isotope, is eluted with an alkali metal salt solution to generate the radioisotope in the form of an intermediate solution, which is passed through the ion-exchange column to convert the radioisotope to a carrier-free acid form.

  20. Laboratory studies of radionuclide migration in tuff

    SciTech Connect (OSTI)

    Rundberg, R.S.; Mitchell, A.J.; Ott, M.A.; Thompson, J.L.; Triay, I.R.

    1989-10-01T23:59:59.000Z

    The movement of selected radionuclides has been observed in crushed tuff, intact tuff, and fractured tuff columns. Retardation factors and dispersivities were determined from the elution profiles. Retardation factors have been compared with those predicted on the basis of batch sorption studies. This comparison forms a basis for either validating distribution coefficients or providing evidence of speciation, including colloid formation. Dispersivities measured as a function of velocity provide a means of determining the effect of sorption kinetics or mass transfer on radionuclide migration. Dispersion is also being studied in the context of scaling symmetry to develop a basis for extrapolating from the laboratory scale to the field. 21 refs., 6 figs., 2 tabs.

  1. Phycocyanin from Chroomonas species purification, electrophoresis and isolation of subunits

    E-Print Network [OSTI]

    Yao, Phyllis Ping-Ching

    1981-01-01T23:59:59.000Z

    of phycocyanobilin and phycoery- throbilin. Page Proposed bilin-protein linkages of' bilip. o- teins Elution profile o phycocyenin or Z. 5 x 95 cmi Sephacryl-200 supe fine at flow rate of 45 mls(hr 21 Vs si'ble-ultraviolet absorption spectrum of Chroomonas.... Attempts to elucidate the nature of the co- valent linkage have included treatment of phycobiliproteins witn reagents which cleave ester, ether and peptide bonds 19-22 as well as isolation and amino acid analyses of chromopeptides obtained...

  2. Turbercidin metabolism in Neurospora crassa

    E-Print Network [OSTI]

    Lyda, Timothy Stuart

    1982-01-01T23:59:59.000Z

    of 14C incorporated into the acid-soluble nucleotide pools of germinated pvr-l, tub conidia incubated with 10 nM [8- 4C] adenosine, 2 pCi/uMol for 20 min 22 g d l g N d~p md' ppl mented with tubercidin (to 100 uM) Anion-exchange elution profile... f ~N d' ppl d with tubercidin (to 100 nial) . Top row (left to right) Ryr-l, tubR ungerminated conidia, conidia germinated 60 min, conidia germinated 4 h. Bottom row (left to right) wild type ungerminated conidia, conidia germinated 60 min...

  3. Statistical Methods for the Analysis of Mass Spectrometry-based Proteomics Data

    E-Print Network [OSTI]

    Wang, Xuan

    2012-07-16T23:59:59.000Z

    . This research is supported by the. This work was sponsored by a subcontract from PNNL and by the NIH R25-CA-90301 training grant at TAMU. Additional support was provided by KAUST-IAMCS Innovation grant, by NIH grant DK070146 and by the National Institute...-MS Liquid chromatographyCMass spectrometry M/Z Mass over charge ratio NET Normalized elution time NMC Number of missed cleavage sites NTE Number of tryptic ends PEP Posterior error probability PM Potential matches PMF Probability mass function PNNL...

  4. Methods, microfluidic devices, and systems for detection of an active enzymatic agent

    DOE Patents [OSTI]

    Sommer, Gregory J; Hatch, Anson V; Singh, Anup K; Wang, Ying-Chih

    2014-10-28T23:59:59.000Z

    Embodiments of the present invention provide methods, microfluidic devices, and systems for the detection of an active target agent in a fluid sample. A substrate molecule is used that contains a sequence which may cleave in the presence of an active target agent. A SNAP25 sequence is described, for example, that may be cleaved in the presence of Botulinum Neurotoxin. The substrate molecule includes a reporter moiety. The substrate molecule is exposed to the sample, and resulting reaction products separated using electrophoretic separation. The elution time of the reporter moiety may be utilized to identify the presence or absence of the active target agent.

  5. Process for removing metals from water

    DOE Patents [OSTI]

    Napier, J.M.; Hancher, C.M.; Hackett, G.D.

    1987-06-29T23:59:59.000Z

    A process for removing metals from water including the steps of prefiltering solids from the water, adjusting the pH to between about 2 and 3, reducing the amount of dissolved oxygen in the water, increasing the pH to between about 6 and 8, adding water-soluble sulfide to precipitate insoluble sulfide- and hydroxide-forming metals, adding a containing floc, and postfiltering the resultant solution. The postfiltered solution may optionally be eluted through an ion exchange resin to remove residual metal ions. 2 tabs.

  6. Supporting Information Moissiard et al. 10.1073/pnas.1406611111

    E-Print Network [OSTI]

    Jacobsen, Steve

    Supporting Information Moissiard et al. 10.1073/pnas.1406611111 FLAG rbcL B atmorc6-1 - AtM ORC6 -FLAG cm t3 - cmt3/ atmorc1-3 GFP C FLAG Input Flowthrough Elution AtM ORC1 -FLAG wild-type 200 400 600MORC5 atm orc2-1 atm orc1-2 FLAG-AtM ORC2 atm orc1-2/atm orc2-1 atm orc1-2/atm orc2-1 w ild-type atm orc

  7. Gas hydrates in the Gulf of Mexico

    E-Print Network [OSTI]

    Cox, Henry Benjamin

    1986-01-01T23:59:59.000Z

    filled by one or more gases. In marine sediments gas hydrates are found in regions where high pressure, low temperature and gas in excess of solubility are present. Low molecular weight hydrocarbons (LMWH), I. e. methane through butane, carbon dioxide... loop at a helium carrier flow of 12 ml/min with an elution order of methane, ethane, carbon dioxide and propane. Each fraction was trapped in a U- shaped Porpak-Q filled glass tube immersed in LN2. Butanes and heartier weight gases were trapped...

  8. A phospho-proteomic screen identifies substrates of the checkpoint kinase Chk1

    E-Print Network [OSTI]

    Blasius, Melanie; Forment, Josep V; Thakkar, Neha; Wagner, Sebastian A; Choudhary, Chunaram; Jackson, Stephen P

    2011-08-18T23:59:59.000Z

    ) for 2 h, 5 ?M etoposide (ETP) for 2 h, 2 mM hydroxyurea (HU) for 12 h, 10 Gy of ionizing radiation (IR) 1 h before harvesting, 60 ?g/ml phleomycin (PHL) for 1 h, or 10 J/m2 of ultraviolet light (UV) 1 h before harvesting. (c) Antibodies against KAP1... were added to trypsin-digested peptides. The beads were extensively washed with 2 ml each of water, 5 M NaCl, 50% acetonitrile, and 5% formic acid in water, sequentially. Phosphopeptides were eluted using 200 ?l of a 1 mg/ml solution of Oxone...

  9. Potential Modulated Intercalation of Alkali Cations into Metal Hexacyanoferrate Coated Electrodes

    SciTech Connect (OSTI)

    Daniel T. Schwartz; Bekki Liu; Marlina Lukman; Kavita M. Jeerage; William A. Steen; Haixia Dai; Qiuming Yu; J. Antonio Medina

    2002-02-18T23:59:59.000Z

    Nickel hexacyanoferrate is a polynuclear inorganic ion intercalation material that loads (intercalates) and elutes (deintercalates) alkali cations from its structure when electrochemically reduced and oxidized, respectively. Nickel hexacyanoferrrate (NiHCF) is known to preferentially intercalate cesium over all other alkali cations, thus providing a basis for a separation scheme that can tackle DOE's radiocesium contamination problem. This program studied fundamental issues in alkalization intercalation and deintercalation in nickel hexacyanoferrate compounds, with the goal of (1) quantifying the ion exchange selectivity properties from cation mixtures, (2) enhancing ion exchange capacities, and (3) and understanding the electrochemically-switched ion exchange process (ESIX).

  10. An Engineering Evaluation of Spherical Resorcinol Formaldehyde Resin

    SciTech Connect (OSTI)

    Birdwell Jr, Joseph F [ORNL; Lee, Denise L [ORNL; Taylor, Paul Allen [ORNL; Collins, Robert T [ORNL; Hunt, Rodney Dale [ORNL

    2010-09-01T23:59:59.000Z

    A small column ion exchange (SCIX) system has been proposed for removal of cesium from caustic, supernatant, and dissolved salt solutions stored or generated from high-level tank wastes at the US Department of Energy (DOE) Hanford Site and Savannah River Sites. In both instances, deployment of SCIX systems, either in-tank or near-tank, is a means of expediting waste pretreatment and dispositioning with minimal or no new infrastructure requirements. Conceptually, the treatment approach can utilize a range of ion exchange media. Previously, both crystalline silicotitanate (CST), an inorganic, nonelutable sorbent, and resorcinol-formaldehyde (RF), an organic, elutable resin, have been considered for cesium removal from tank waste. More recently, Pacific Northwest National Laboratory (PNNL) evaluated use of SuperLig{reg_sign} 644, an elutable ion exchange medium, for the subject application. Results of testing indicate hydraulic limitations of the SuperLig{reg_sign} resin, specifically a high pressure drop through packed ion exchange columns. This limitation is likely the result of swelling and shrinkage of the irregularly shaped (granular) resin during repeated conversions between sodium and hydrogen forms as the resin is first loaded then eluted. It is anticipated that a similar flow limitation would exist in columns packed with conventional, granular RF resin. However, use of spherical RF resin is a likely means of mitigating processing limitations due to excessive pressure drop. Although size changes occur as the spherical resin is cycled through loading and elution operations, the geometry of the resin is expected to effectively mitigate the close packing that leads to high pressure drops across ion exchange columns. Multiple evaluations have been performed to determine the feasibility of using spherical RF resin and to obtain data necessary for design of an SCIX process. The work performed consisted of examination of radiation effects on resin performance, quantification of cesium adsorption performance as a function of operating temperature and pH, and evaluation of sodium uptake (titration) as function of pH and counteranion concentration. The results of these efforts are presented in this report. Hydraulic performance of the resin and the use of eluant alternatives to nitric acid have also been evaluated and have been reported elsewhere (Taylor 2009, Taylor and Johnson 2009).

  11. Selective enrichment of phenols from coal liquefaction oil by solid phase extraction method

    SciTech Connect (OSTI)

    Tian, M.; Feng, J. [Taiyuan University of Technoloy, Taiyuan (China)

    2009-07-01T23:59:59.000Z

    This study focuses on the solid phase extraction method for the enrichment and separation of phenol from coal liquefaction oil. The phenols' separation efficiency was compared on different solid phase extraction (SPE) cartridges, and the effect of solvents with different polarity and solubility parameter on amino-bonded silica was compared for selection of optimal elution solution. The result showed that amino-bonded silica has the highest selectivity and best extraction capability due to two factors, weak anion exchange adsorption and polar attraction adsorption.

  12. Synthesis of N-carbobenzoxy-L-valyl-L-valyl-4-amino-3-hydroxy-5-methylhexanoic acid

    E-Print Network [OSTI]

    Hicks, Gary Dean

    1980-01-01T23:59:59.000Z

    , and dried over sodium sulfate. The sol- vent was removed by evaporation in vacuo and the products isolated by silica gel chromatography, eluting with 25% ethyl acetate/hexane, to give the following results: Ethyl (38, 4S)-N-t-butyloxycarbonyl-4-amino-3... columns prepacked with silica gel 60 (EM Reagents). Amino acids were coupled using mixed anhydride coupling methods. ACKNOWLEDGMENTS The author is grateful to Dr, G. I. Glover for all the guidance and support he has provided, A special thanks to Dr, E...

  13. Tungsten-188/carrier-free rhenium-188 perrhenic acid generator system

    DOE Patents [OSTI]

    Knapp, F.F. Jr.; Lisic, E.C.; Mirzadeh, S.; Callahan, A.P.

    1993-02-16T23:59:59.000Z

    A generator system for providing a carrier-free radioisotope in the form of an acid comprises a chromatography column in tandem fluid connection with an ion exchange column, the chromatography column containing a charge of a radioactive parent isotope. The chromatography column, charged with a parent isotope, is eluted with an alkali metal salt solution to generate the radioisotope in the form of an intermediate solution, which is passed through the ion-exchange column to convert the radioisotope to a carrier-free acid form.

  14. Tungsten-188/carrier-free rhenium-188 perrhenic acid generator system

    DOE Patents [OSTI]

    Knapp, F.F. Jr.; Lisic, E.C.; Mirzadeh, S.; Callahan, A.P.

    1994-01-04T23:59:59.000Z

    A generator system has been invented for providing a carrier-free radioisotope in the form of an acid comprises a chromatography column in tandem fluid connection with an ion exchange column, the chromatography column containing a charge of a radioactive parent isotope. The chromatography column, charged with a parent isotope, is eluted with an alkali metal salt solution to generate the radioisotope in the form of an intermediate solution, which is passed through the ion-exchange column to convert the radioisotope to a carrier-free acid form. 1 figure.

  15. Planning study, resin and debris removal system. Three Mile Island nuclear station unit 2 make-up and purification demineralizers

    SciTech Connect (OSTI)

    Renkey, E.J.; Jenkins, W.W.

    1983-06-01T23:59:59.000Z

    Various methods were evaluated to remove the resin and debris from the makeup and purification demineralizers. There are two preferred concepts. The existing waste disposal system should be utilized if some contamination of currently clean lines is acceptable. A skid mounted, temporary, upflow/downflow system should be utilized if the demineralizers and associated piping are to be cleaned to the maximum extent practicable with minimum contamination of the existing system. Both methods provide for removal of complex organic compounds from the effluent and elution of cesium from the resin. The resin and debris will be diluted with concrete to be disposed of in accordance with 10CFR61 burial limits.

  16. Ion exchange purification of scandium

    DOE Patents [OSTI]

    Herchenroeder, L.A.; Burkholder, H.R.

    1990-10-23T23:59:59.000Z

    An improvement in purification of scandium through ion exchange chromatography is disclosed in which the oxidation potential of the eluting solution is altered by the addition of potassium chlorate or ammonium chloride so that removal of contaminants is encouraged. The temperature, pH and concentration of the eluent HEDTA are controlled in order to maintain the scandium in the column while minimizing dilution of the scandium band. Recovery of scandium is improved by pumping dilute scandium over the column prior to stripping the scandium and precipitation. This eliminates the HEDTA ion and other monovalent cations contaminating the scandium band. This method maximizes recovery of scandium while maintaining purity. 2 figs.

  17. EMPORA 1 + 2 EMobile Power Austria (Smart Grid Project) (Graz, Austria) |

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 NoPublic Utilities Address:011-DNA Jump37. It is classified as ASHRAEDuval County,EEnergy(Redirected fromELUTIONS

  18. Development of an in vitro model for migration inhibitory factor utilizing a component of cobra venom

    E-Print Network [OSTI]

    Carmack, Lee James

    1976-01-01T23:59:59.000Z

    of Committee~ Head of Depar me j'7 c Member Membe May 1976 ABSTRACT Development of an In Vitro Model for Migration Inhibitory Factor Utilizing a Component of Cobra Venon. May (1976) Lee James Carmack, B. S. , Texas ASM University; Chairman of Advisory... of fractions eluted from the ion exchange column 2 Effects of whole cobra venom (CV), dialyzed cobra venom (OCV), Arvin, and Venacil on migration of normal mouse peritoneal exudate cells in cell culture 3 Effects on migration of normal mouse peritoneal...

  19. Identification and functional characterization of lipid binding proteins in liver and adipose tissues of Gallus domesticus

    E-Print Network [OSTI]

    Sams, Gretchen Hubler

    1990-01-01T23:59:59.000Z

    ; whereas the second hepatic lipid transport protein is most likely liver-FABP (L-FABP). An FABP from chicken adipose cytosol (A-FABP) was purified by membrane ultrafiltration and molecular sieve chromatography. Purification was verified by SDS... via ion exchange chromatography, pH 7. 73. Purification was verified by ligand binding assays and SDS-PAGE. The first protein eluted (designated ns-LTP) had a molecular weight of approximately 14. 5 kDa and the second protein (designated L...

  20. Chemical Properties of Elements 99 and 100 [Einsteinium and Fermium

    DOE R&D Accomplishments [OSTI]

    Seaborg, G. T.; Thompson, S. G.; Harvey, B. G.; Choppin, G. R.

    1954-07-23T23:59:59.000Z

    A description of some of the chemical properties and of the methods used in the separations of elements 99 [Einsteinium] and 100 [Fermium] are given. The new elements exhibit the properties expected for the tenth and eleventh actinide elements. Attempts to produce an oxidation state greater than III of element 99 have been unsuccessful. In normal aqueous media only the III state of element 100 appears to exist. The relative spacings of the elution peaks of the new elements in some separations with ion exchange resin columns are the same as the relative spacings of the homologous lanthanide elements. The results of experiments involving cation exchange resins with very concentrated hydrochloric acid eluant show that the new elements, like the earlier actinides, are more strongly complexed than the lanthanides. The new elements also exist partially as anions in concentrated hydrochloric acid, as do earlier actinide elements, and they may be partially separated from each other by means of ion exchange resins. With some eluants interesting reversals of elution positions are observed in the region Bk-Cf-99-100, indicating complex ion formation involving unusual factors.

  1. Interpretation of data obtained from non-destructive and destructive post-test analyses of an intact-core column of culebra dolomite

    SciTech Connect (OSTI)

    Lucero, Daniel L.; Perkins, W. George

    1998-09-01T23:59:59.000Z

    The U.S. Department of Energy (DOE) has been developing a nuclear waste disposal facility, the Waste Isolation Pilot Plant (WIPP), located approximately 42 km east of Carlsbad, New Mexico. The WIPP is designed to demonstrate the safe disposal of transuranic wastes produced by the defense nuclear-weapons program. Pefiormance assessment analyses (U.S. DOE, 1996) indicate that human intrusion by inadvertent and intermittent drilling for resources provide the only credible mechanisms for significant releases of radionuclides horn the disposal system. These releases may occur by five mechanisms: (1) cuttings, (2) cavings, (3) spallings, (4) direct brine releases, and (5) long- term brine releases. The first four mechanisms could result in immediate release of contaminant to the accessible environment. For the last mechanisq migration pathways through the permeable layers of rock above the Salado are important, and major emphasis is placed on the Culebra Member of the Rustler Formation because this is the most transmissive geologic layer in the disposal system. For reasons of initial quantity, half-life, and specific radioactivity, certain isotopes of T~ U, Am, and Pu would dominate calculated releases from the WIPP. In order to help quantifi parameters for the calculated releases, radionuclide transport experiments have been carried out using five intact-core columns obtained from the Culebra dolomite member of the Rustler Formation within the Waste Isolation Pilot Pknt (WIPP) site in southeastern New Mexico. This report deals primarily with results of analyses for 241Pu and 241Am distributions developed during transport experiments in one of these cores. All intact-core column transport experiments were done using Culebra-simukmt brine relevant to the core recovery location (the WIPP air-intake shaft - AK). Hydraulic characteristics (i.e., apparent porosity and apparent dispersion coefficient) for intact-core columns were obtained via experiments using conservative tracer `Na. Elution experiments carried out over periods of a few days with tracers `2U and `?Np indicated that these tracers were weakly retarded as indicated by delayed elution of these species. Elution experiments with tracers 24% and 24*Arn were performed, but no elution of either species was observed in any flow experiment to date, including experiments of many months' duration. In order to quanti~ retardation of the non-eluted species 24*Pu and 241Arn afler a period of brine flow, non-destructive and destructive analyses of an intact-core column were carried out to determine distribution of these actinides in the rock. Analytical results indicate that the majority of the 241Am is present very near the top (injection) surface of the core (possibly as a precipitate), and that the majority of the 241Pu is dispersed with a very high apparent retardation value. The 24]Pu distribution is interpreted using a single-porosity advection-dispersion model, and an approximate retardation value is reported for this actinide. The specific radionuclide isotopes used in these experiments were chosen to facilitate analysis. Even though these isotopes are not necessarily the same as those that are most important to WIPP performance, they are isotopes of the same elements, and their chemical and transport properties are therefore identical to those of isotopes in the inventory.

  2. Affordable Hydrogen Fuel Cell Vehicles: Quaternary Phosphonium Based Hydroxide Exchange Membranes

    SciTech Connect (OSTI)

    None

    2010-01-01T23:59:59.000Z

    Broad Funding Opportunity Announcement Project: The University of Delaware is developing a new fuel cell membrane for vehicles that relies on cheaper and more abundant materials than those used in current fuel cells. Conventional fuel cells are very acidic, so they require acid-resistant metals like platinum to generate electricity. The University of Delaware is developing an alkaline fuel cell membrane that can operate in a non-acidic environment where cheaper materials like nickel and silver, instead of platinum, can be used. In addition to enabling the use of cheaper metals, the University of Delawares membrane is 500 times less expensive than other polymer membranes used in conventional fuel cells.

  3. CHARACTERIZATION OF CYCLED SPHERICAL RESORCINOL-FORMALDEHYDE ION EXCHANGE RESIN

    SciTech Connect (OSTI)

    Nash, C.; Duignan, M.

    2010-02-23T23:59:59.000Z

    This report presents characterization data for two spherical resorcinol-formaldehyde (sRF) resin beds that had processed cesium in non-radioactive and radioactive cycles. All column cycle operations for the resin beds including loading, displacements, elution, regeneration, breakthroughs, and solution analyses are reported in Nash and Duignan, 2009a. That report covered four ion exchange (IX) campaigns using the two {approx}11 mL beds in columns in a lead-lag arrangement. The first two campaigns used Savannah River Site (SRS) Tank 2F nonradioactive simulant while the latter two were fed with actual dissolved salt in the Savannah River National Laboratory (SRNL) Shielded Cells. Both radioactive cycles ran to cesium breakthrough of the lead column. The resin beds saw in excess of 400 bed volumes of feed in each cycle. Resin disposal plans in tank farm processing depend on characterizations of resin used with actual tank feed. Following a final 30 bed volume (BV) elution with nitric acid, the resin beds were found to contain detectable chromium, barium, boron, aluminum, iron, sodium, sulfur, plutonium, cesium, and mercury. Resin affinity for plutonium is important in criticality safety considerations. Cesium-137 was found to be less than 10E+7 dpm/g of resin, similar to past work with sRF resin. Sulfur levels are reasonably consistent with other work and are expected to represent sulfur chemistry used in the resin manufacture. There were low but detectable levels of technetium, americium, and curium. Toxicity Characteristic Leaching Procedure (TCLP) work on the used (eluted) resin samples showed significant contents of mercury, barium, and chromium. One resin sample exceeded the TCLP level for mercury while the other metals were below TCLP levels. TCLP organics measurements indicated measurable benzene in one case, though the source was unknown. Results of this work were compared with other work on similar sRF resin characterizations in this report. This is the first work to quantify mercury on sRF resin. Resin mercury content is important in plans for the disposition of used sRF resin. Mercury speciation in high level waste (HLW) is unknown. It may be partly organic, one example being methyl mercury cation. Further study of the resin's affinity for mercury is recommended.

  4. REAL WASTE TESTING OF SPHERICAL RESORCINOL-FORMALDEHYDE ION EXCHANGE RESIN

    SciTech Connect (OSTI)

    Nash, C.; Duignan, M.

    2009-10-30T23:59:59.000Z

    This report presents data on batch contact and column testing tasks for spherical resorcinol-formaldehyde (sRF) resin. The testing used a non-radioactive simulant of SRS Tank 2F dissolved salt, as well as an actual radioactive waste sample of similar composition, which are both notably high in sodium (6 M). The resin was Microbeads batch 5E-370/641 which had been made on the hundred gallon scale. Equilibrium batch contact work focused on cesium at a temperature of 25 C due to the lack of such data to better benchmark existing isotherm models. Two campaigns were performed with small-scale ion exchange columns, first with Tank 2F simulant, then with actual dissolved salt in the Shielded Cells. An extrapolation of the batch contact results with radioactive waste over-predicted the cesium loaded onto the IX sRF resin bed by approximately 11%. This difference is not unexpected considering uncertainties from measurement and extrapolation and because the ion exchange that occurs when waste flows through a resin bed probably cannot reach the same level of equilibrium as when waste and resin are joined in a long term batch contact. Resin was also characterized to better understand basic chemistry issues such as holdup of trace transition metals present in the waste feed streams. The column tests involved using two beds of sRF resin in series, with the first bed referred to as the Lead column and the second bed as the Lag column. The test matrix included two complete IX cycles for both the simulant and actual waste phases. A cycle involves cesium adsorption, until the resin in the Lead column reaches saturation, and then regenerating the sRF resin, which includes eluting the cesium. Both the simulated and the actual wastes were treated with two cycles of operation, and the resin beds that were used in the Lead and Lag columns of simulant test phase were regenerated and reused in the actual waste test phase. This task is the first to demonstrate the treatment of SRS waste with sRF resin and the tests clearly demonstrated cesium decontamination for actual waste. The results of the column tests were similar for both the simulated and the actual waste and demonstrated Cs removal with sRF from both wastes. For a flowrate of 1.4 bed volumes (BV)/hour at 25 C those results with sRF resin were: (1) Simulant and actual waste results are equivalent; (2) Cs breakthrough began between 200 and 250 BV; (3) Cs breakthrough reached 100% at around 400 BV; (4) Cs breakthrough curve from 5% to 100% is approximately linear; (5) Cs elution with 0.5 M HNO3 starts at 2 BV and ends at 6BV; (6) Most, if not all, of Cs adsorbed during treatment is released during elution; (7) At 100% breakthrough of Cs the resin bed adsorbs approximately 85% of full capacity before detection in the effluent; the remaining 15% is adsorbed at saturation; (8) Approximately 90% of resin bed changes (color and volume) are complete by 6 BV; and (9) During elution the resin shrinks to about 80% of its fully working (sodium form) BV.

  5. Intercalation of Trichloroethene by Sediment-Associated Clay Minerals

    SciTech Connect (OSTI)

    Matthieu, Donald E.; Brusseau, Mark; Johnson, G. R.; Artiola, J. L.; Bowden, Mark E.; Curry, J. E.

    2013-01-01T23:59:59.000Z

    The objective of this research was to examine the potential for intercalation of trichloroethene (TCE) by clay minerals associated with aquifer sediments. Sediment samples were collected from a field site inTucson, AZ. Two widely used Montmorillonite specimen clays were employed as controls. X-ray diffraction, conducted with a controlled-environment chamber, was used to characterize smectite interlayer dspacing for three treatments (bulk air-dry sample, sample mixed with synthetic groundwater, sample mixed with TCE-saturated synthetic groundwater). The results show that the d-spacing measured for the samples treated with TCE-saturated synthetic groundwater are larger (*26%) than those of the untreated samples for all field samples as well as the specimen clays. These results indicate that TCE was intercalated by the clay minerals, which may have contributed to the extensive elution tailing observed in prior miscible-displacement experiments conducted with this sediment.

  6. Influence of Contact Time on the Extraction of 233Uranyl Spike and Contaminant Uranium From Hanford Sediment

    SciTech Connect (OSTI)

    Smith, Steven C.; Szecsody, James E.

    2011-11-01T23:59:59.000Z

    In this study 233Uranyl nitrate was added to uranium (U) contaminated Hanford 300 Area sediment and incubated under moist conditions for 1 year. It hypothesized that geochemical transformations and/or physical processes will result in decreased extractability of 233U as the incubation period increases, and eventually the extraction behavior of the 233U spike will be congruent to contaminant U that has been associated with sediment for decades. Following 1 week, 1 month, and 1 year incubation periods, sediment extractions were performed using either batch or dynamic (sediment column flow) chemical extraction techniques. Overall, extraction of U from sediment using batch extraction was less complicated to conduct compared to dynamic extraction, but dynamic extraction could distinguish the range of U forms associated with sediment which are eluted at different times.

  7. Tanks Focus Area Alternative Salt Processing Research and Development Program Plan

    SciTech Connect (OSTI)

    Harmon, Harry D.

    2000-11-30T23:59:59.000Z

    In March 2000, DOE-Headquarters (HQ) requested the Tanks Focus Area (TFA) to assume management responsibility for the Salt Processing Project technology development program at Savannah River Site. The TFA was requested to conduct several activities, including review and revision of the technology development roadmaps, development of down-selection criteria, and preparation of a comprehensive Research and Development (R&D) Program Plan for three candidate cesium removal technologies, as well as the Alpha and strontium removal processes that must also be carried out. The three cesium removal candidate technologies are Crystalline Silicotitanate (CST) Non-Elutable Ion Exchange, Caustic Side Solvent Extraction (CSSX), and Small Tank Tetraphenylborate Precipitation (STTP). This plan describes the technology development needs for each process that must be satisfied in order to reach a down-selection decision, as well as continuing technology development required to support conceptual design activities.

  8. Tanks Focus Area Alternative Salt Processing Research and Development Program Plan

    SciTech Connect (OSTI)

    Harmon, Harry D.

    2000-05-15T23:59:59.000Z

    In March 2000, DOE-Headquarters (HQ) requested the Tanks Focus Area (TFA)to assume management responsibility for the Salt Processing Project technology development program at Savannah River Site. The TFA was requested to conduct several activities, including review and revision of the technology development roadmaps, development of down-selection criteria, and preparation of a comprehensive Research and Development (R&D) Program Plan for three candidate cesium removal technologies, as well as the Alpha and strontium removal processes that must also be carried out. The three cesium removal candidate technologies are Crystalline Silicotitanate (CST) Non-Elutable Ion Exchange, Caustic Side Solvent Extraction (CSSX), and Small Tank Tetraphenylborate Precipitation (STTP). This plan describes the technology development needs for each process that must be satisfied in order to reach a down-selection decision, as well as continuing technology development required to support conceptual design activities.

  9. Use of Chelex-100 for selectively removing Y-90 from its parent Sr-90

    DOE Patents [OSTI]

    Huntley, M.W.

    1996-02-27T23:59:59.000Z

    A method for selectively removing yttrium-90 from its parent strontium-90 contained in an environmental sample includes loading the sample onto a column containing a chelating ion-exchange resin capable of retaining yttrium-90; washing the column with a solution capable of removing strontium, calcium, and other contaminants from the yttrium-90 fraction retained on the column; removing excess acetate salts from the column; eluting yttrium-90 solution from the column and adjusting the pH of this solution to about 2.7; filtering the yttrium-90 solution and weighing this solution for gravimetric yield; and, counting the yttrium-90 containing solution with a radiological counter for a time sufficient to achieve the statistical accuracy desired. It is preferred that the chelating ion-exchange resin is a ligand having the chemical name iminodiacetic acid mounted on a divinyl benzene substrate, converted from sodium form to ammonia form.

  10. Use of Chelex-100 for selectively removing Y-90 from its parent Sr-90

    DOE Patents [OSTI]

    Huntley, Mark W. (Idaho Falls, ID)

    1996-01-01T23:59:59.000Z

    A method for selectively removing yttrium-90 from its parent strontium-90 contained in an environmental sample includes loading the sample onto a column containing a chelating ion-exchange resin capable of retaining yttrium-90; washing the column with a solution capable of removing strontium, calcium, and other contaminants from the yttrium-90 fraction retained on the column; removing excess acetate salts from the column; eluting yttrium-90 solution from the column and adjusting the pH of this solution to about 2.7; filtering the yttrium-90 solution and weighing this solution for gravimetric yield; and, counting the yttrium-90 containing solution with a radiological counter for a time sufficient to achieve the statistical accuracy desired. It is preferred that the chelating ion-exchange resin is a bidente ligand having the chemical name iminodiacetic acid mounted on a divinyl benzene substrate, converted from sodium form to ammonia form.

  11. Method for the chemical separation of GE-68 from its daughter Ga-68

    DOE Patents [OSTI]

    Fitzsimmons, Jonathan M.; Atcher, Robert W.

    2010-06-01T23:59:59.000Z

    The present invention is directed to a generator apparatus for separating a daughter gallium-68 radioisotope substantially free of impurities from a parent gernanium-68 radioisotope, including a first resin-containing column containing parent gernanium-68 radioisotope and daughter gallium-68 radioisotope, a source of first eluent connected to said first resin-containing column for separating daughter gallium-68 radioisotope from the first resin-containing column, said first eluent including citrate whereby the separated gallium is in the form of gallium citrate, a mixing space connected to said first resin-containing column for admixing a source of hydrochloric acid with said separated gallium citrate whereby gallium citrate is converted to gallium tetrachloride, a second resin-containing column for retention of gallium-68 tetrachloride, and, a source of second eluent connected to said second resin-containing column for eluting the daughter gallium-68 radioisotope from said second resin-containing column.

  12. Features of the adsoprtion of naproxen on the chiral stationary phase (S,S)-Whelk-O1 under reversed-phase conditions

    SciTech Connect (OSTI)

    Asnin, Leonid [University of Tennessee, Knoxville (UTK); Gritti, Fabrice [University of Tennessee, Knoxville (UTK); Kaczmarski, Krzysztof [University of Tennessee and Rzeszow University of Technology, Poland; Guiochon, Georges A [ORNL

    2010-01-01T23:59:59.000Z

    Using elution chromatography, we studied the adsorption mechanism of the Naproxen enantiomers on the chiral stationary phase (S,S)-Whelk-O1, from buffered methanol-water solutions. We propose an adsorption mechanism that assumes monolayer adsorption of the more retained enantiomer and the associative adsorption of the less retained one. The effects of the mobile phase composition on the adsorption of Naproxen are discussed. The combination of an elevated column temperature and of the use of an acidic mobile phase led to the degradation of the column and caused a major loss of its separation ability. The use of a moderately acidic mobile phase at temperature slightly above ambient did not produce rapid severe damages but, nevertheless, hampered the experiments and caused a slow gradual deterioration of the column.

  13. FINAL SUMMARIZING REPORT on Grant DE-SC0001014 "Separation of Highly Complex Mixtures by Two-dimension Liquid Chromatography"

    SciTech Connect (OSTI)

    Guiochon, Georges

    2013-09-16T23:59:59.000Z

    The goal of our research was a fundamental investigation of methods available for the coupling of two separate chromatographic separations that would considerably enhance the individual separation power of each of these two separations. This gain arises from the combination of two independent retention mechanisms, one of them separating the components that coelute on the other column, making possible the separation of many more compounds in a given time. The two separation mechanisms used must be very different. This is possible because many retention mechanisms are available, using different kinds of molecular interactions, hydrophobic or hydrophilic interactions, polar interactions, hydrogen bonding, complex formation, ionic interactions, steric exclusion. Two methods can be used, allowing separations to be performed in space (spreading the bands of sample components on a plate covered with stationary phase layer) or in time (eluting the sample components through a column and detecting the bands leaving the column). Both offer a wide variety of possible combinations and were studied.

  14. Method for digesting spent ion exchange resins and recovering actinides therefrom using microwave radiation

    DOE Patents [OSTI]

    Maxwell, III, Sherrod L. (Aiken, SC); Nichols, Sheldon T. (Augusta, GA)

    1999-01-01T23:59:59.000Z

    The present invention relates to methods for digesting diphosphonic acid substituted cation exchange resins that have become loaded with actinides, rare earth metals, or heavy metals, in a way that allows for downstream chromatographic analysis of the adsorbed species without damage to or inadequate elution from the downstream chromatographic resins. The methods of the present invention involve contacting the loaded diphosphonic acid resin with concentrated oxidizing acid in a closed vessel, and irradiating this mixture with microwave radiation. This efficiently increases the temperature of the mixture to a level suitable for digestion of the resin without the use of dehydrating acids that can damage downstream analytical resins. In order to ensure more complete digestion, the irradiated mixture can be mixed with hydrogen peroxide or other oxidant, and reirradiated with microwave radiation.

  15. Method for regeneration of electroless nickel plating solution

    SciTech Connect (OSTI)

    Eisenmann, Erhard T. (5423 Vista Sandia, NE., Albuquerque, NM 87111)

    1997-01-01T23:59:59.000Z

    An electroless nickel(EN)/hypophosphite plating bath is provided employing acetic acid/acetate as a buffer and which is, as a result, capable of perpetual regeneration while avoiding the production of hazardous waste. A regeneration process is provided to process the spent EN plating bath solution. A concentrated starter and replenishment solution is provided for ease of operation of the plating bath. The regeneration process employs a chelating ion exchange system to remove nickel cations from spent EN plating solution. Phosphites are then removed from the solution by precipitation. The nickel cations are removed from the ion exchange system by elution with hypophosphorous acid and the nickel concentration of the eluate adjusted by addition of nickel salt. The treated solution and adjusted eluate are combined, stabilizer added, and the volume of resulting solution reduced by evaporation to form the bath starter and replenishing solution.

  16. Method for regeneration of electroless nickel plating solution

    SciTech Connect (OSTI)

    Eisenmann, E.T.

    1997-03-11T23:59:59.000Z

    An electroless nickel(EN)/hypophosphite plating bath is provided employing acetic acid/acetate as a buffer and which is, as a result, capable of perpetual regeneration while avoiding the production of hazardous waste. A regeneration process is provided to process the spent EN plating bath solution. A concentrated starter and replenishment solution is provided for ease of operation of the plating bath. The regeneration process employs a chelating ion exchange system to remove nickel cations from spent EN plating solution. Phosphites are then removed from the solution by precipitation. The nickel cations are removed from the ion exchange system by elution with hypophosphorus acid and the nickel concentration of the eluate adjusted by addition of nickel salt. The treated solution and adjusted eluate are combined, stabilizer added, and the volume of resulting solution reduced by evaporation to form the bath starter and replenishing solution. 1 fig.

  17. Simple procedures for enrichment of chlorinated aromatic pollutants from fat, water and milk for subsequent analysis by high-resolution methods

    SciTech Connect (OSTI)

    Egestad, B.; Curstedt, T.; Sjoevall, J.

    1982-01-01T23:59:59.000Z

    Procedures for enrichment of non-volatile chlorinated aromatic pollutants from fat, water and milk are described. /sup 14/C-DDT was used as a model compound in recovery experiments. A several thousand-fold enrichment of DDT added to butter was achieved by two consecutive straight-phase chromatographies on Lipidex 5000. Trace amounts of DDT in liter volumes of water could be quantitatively extracted by rapid filtration through 2 ml beds of Lipidex 1000. A batch extraction procedure permitted enrichment of DDT from milk after addition of n-pentylamine, methanol and water. DDT could then be eluted from the gel with retention of more than 90% of the lipids. A reversed-phase system with Lipidex 5000 could be used for separation of TCDD from DDT and PCBs. The liquid-gel chromatographic procedures are simple and suitable for clean-up of samples prior to application of high-resolution methods. 5 tables.

  18. Method for determining asphaltene stability of a hydrocarbon-containing material

    DOE Patents [OSTI]

    Schabron, John F; Rovani, Jr., Joseph F

    2013-02-05T23:59:59.000Z

    A method for determining asphaltene stability in a hydrocarbon-containing material having solvated asphaltenes therein is disclosed. In at least one embodiment, it involves the steps of: (a) precipitating an amount of the asphaltenes from a liquid sample of the hydrocarbon-containing material with an alkane mobile phase solvent in a column; (b) dissolving a first amount and a second amount of the precipitated asphaltenes by changing the alkane mobile phase solvent to a final mobile phase solvent having a solubility parameter that is higher than the alkane mobile phase solvent; (c) monitoring the concentration of eluted fractions from the column; (d) creating a solubility profile of the dissolved asphaltenes in the hydrocarbon-containing material; and (e) determining one or more asphaltene stability parameters of the hydrocarbon-containing material.

  19. Fluidics platform and method for sample preparation and analysis

    DOE Patents [OSTI]

    Benner, W. Henry; Dzenitis, John M.; Bennet, William J.; Baker, Brian R.

    2014-08-19T23:59:59.000Z

    Herein provided are fluidics platform and method for sample preparation and analysis. The fluidics platform is capable of analyzing DNA from blood samples using amplification assays such as polymerase-chain-reaction assays and loop-mediated-isothermal-amplification assays. The fluidics platform can also be used for other types of assays and analyzes. In some embodiments, a sample in a sealed tube can be inserted directly. The following isolation, detection, and analyzes can be performed without a user's intervention. The disclosed platform may also comprises a sample preparation system with a magnetic actuator, a heater, and an air-drying mechanism, and fluid manipulation processes for extraction, washing, elution, assay assembly, assay detection, and cleaning after reactions and between samples.

  20. Repair of gamma-ray-induced DNA base damage in xeroderma pigmentosum cells

    SciTech Connect (OSTI)

    Fornace, A.J. Jr.; Dobson, P.P.; Kinsella, T.J.

    1986-04-01T23:59:59.000Z

    The repair of DNA damage produced by /sup 137/Cs gamma irradiation was measured with a preparation from Micrococcus luteus containing DNA damage-specific endonucleases in combination with alkaline elution. The frequency of these endonuclease sensitive sites (ESS) was determined after 54 or 110 Gy of oxic irradiation in normal and xeroderma pigmentosum (XP) fibroblasts from complementation groups A, C, D, and G. Repair was rapid in all cell strains with greater than 50% repair after 1.5 h of repair incubation. At later repair times, 12-17 h, more ESS remained in XP than in normal cells. The frequency of excess ESS in XP cells was approximately 0.04 per 10(9) Da of DNA per Gy which was equivalent to 10% of the initial ESS produced. The removal of ESS was comparable in XP cells with normal radiosensitivity and XP3BR cells which have been reported to be moderately radiosensitive.

  1. The identification and quantitative analysis of the very toxic 2,3,7,8-tetrachlorodibenzo-p-dioxin in the presence of polychlorinated dibenzodioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) contaminated soil samples

    SciTech Connect (OSTI)

    Pehlivan, M.; Pehlivan, E. [Selcuk Univ., Konya (Turkey); Oezler, M.A. [Muola Univ., Mugla (Turkey); Barlas, H. [Istanbul Univ. (Turkey)

    1999-02-01T23:59:59.000Z

    This research describes the nature and extent of 2,3,7,8-tetrachlorodibenzo-p-dioxin (2,3,7,8-TCDD) contamination in the soil samples from a waste cable incineration plant. The samples are collected at different places in the nearest and far away points of the soil around the incineration plant. A procedure which is described for the selective separation of 2,3,7,8-TCDD from all other PCDDs and PCDFs fractionated on Alumina Woelm B Super 1 in such a manner that all PCDDs are eluted prior to 2,3,7,8-TCDD. This procedure allows more sensitive quantitative determination of 2,3,7,8-TCDD in the soil samples.

  2. Pretreatment/Radionuclide Separations of Cs/Tc from Supernates

    SciTech Connect (OSTI)

    Thompson, M.C. [Westinghouse Savannah River Company, AIKEN, SC (United States)

    1998-09-01T23:59:59.000Z

    Significant improvements have been made in ion exchange and solvent extraction materials and processes available for separation of the radionuclides cesium and technetium from both acid and alkaline waste solutions. New ion exchange materials and solvent extraction reagents are more selective for Cs over sodium and potassium than previous materials. The higher selectivity gives higher Cs capacity and improved separation processes. Technetium removal has been improved by new ion exchange resins, which have either improved capacity or easier elution. Several different crown ethers have been shown to extract pertechnetate ion selectively over other anions. Organic complexants in some waste solutions reduce pertechnetate ion and stabilize the reduced species. Selective oxidation allows conversion to pertechnetate without oxidation of the organic complexants.

  3. Regeneration of strong-base anion-exchange resins by sequential chemical displacement

    DOE Patents [OSTI]

    Brown, Gilbert M. (Knoxville, TN); Gu, Baohua (Oak Ridge, TN); Moyer, Bruce A. (Oak Ridge, TN); Bonnesen, Peter V. (Knoxville, TN)

    2002-01-01T23:59:59.000Z

    A method for regenerating strong-base anion exchange resins utilizing a sequential chemical displacement technique with new regenerant formulation. The new first regenerant solution is composed of a mixture of ferric chloride, a water-miscible organic solvent, hydrochloric acid, and water in which tetrachloroferrate anion is formed and used to displace the target anions on the resin. The second regenerant is composed of a dilute hydrochloric acid and is used to decompose tetrachloroferrate and elute ferric ions, thereby regenerating the resin. Alternative chemical displacement methods include: (1) displacement of target anions with fluoroborate followed by nitrate or salicylate and (2) displacement of target anions with salicylate followed by dilute hydrochloric acid. The methodology offers an improved regeneration efficiency, recovery, and waste minimization over the conventional displacement technique using sodium chloride (or a brine) or alkali metal hydroxide.

  4. Sampling probe for microarray read out using electrospray mass spectrometry

    DOE Patents [OSTI]

    Van Berkel, Gary J.

    2004-10-12T23:59:59.000Z

    An automated electrospray based sampling system and method for analysis obtains samples from surface array spots having analytes. The system includes at least one probe, the probe including an inlet for flowing at least one eluting solvent to respective ones of a plurality of spots and an outlet for directing the analyte away from the spots. An automatic positioning system is provided for translating the probe relative to the spots to permit sampling of any spot. An electrospray ion source having an input fluidicly connected to the probe receives the analyte and generates ions from the analyte. The ion source provides the generated ions to a structure for analysis to identify the analyte, preferably being a mass spectrometer. The probe can be a surface contact probe, where the probe forms an enclosing seal along the periphery of the array spot surface.

  5. Non-planar microfabricated gas chromatography column

    DOE Patents [OSTI]

    Lewis, Patrick R. (Albuquerque, NM); Wheeler, David R. (Albuquerque, NM)

    2007-09-25T23:59:59.000Z

    A non-planar microfabricated gas chromatography column comprises a planar substrate having a plurality of through holes, a top lid and a bottom lid bonded to opposite surfaces of the planar substrate, and inlet and outlet ports for injection of a sample gas and elution of separated analytes. A plurality of such planar substrates can be aligned and stacked to provide a longer column length having a small footprint. Furthermore, two or more separate channels can enable multi-channel or multi-dimensional gas chromatography. The through holes preferably have a circular cross section and can be coated with a stationary phase material or packed with a porous packing material. Importantly, uniform stationary phase coatings can be obtained and band broadening can be minimized with the circular channels. A heating or cooling element can be disposed on at least one of the lids to enable temperature programming of the column.

  6. New Treatments for Infrapopliteal Disease: Devices, Techniques, and Outcomes So Far

    SciTech Connect (OSTI)

    Bernstein, Ondina; Chalmers, Nicholas, E-mail: nicholas.chalmers@cmft.nhs.uk [Manchester Royal Infirmary, Department of Radiology (United Kingdom)

    2012-08-15T23:59:59.000Z

    The use of endovascular treatment of infrapopliteal disease has increased in popularity in recent years. An improvement in technical success rates due to the availability of newer devices has fuelled an increased interest in the subject. The pathogenesis, indications for treatment, and outcome measures of infrapopliteal disease differ from larger vessel intervention. Diabetes and renal failure are prevalent. Neuropathy and venous disease contribute to the etiology of ulceration. Most interventions are undertaken for critical limb ischemia rather than claudication. Therefore, a range of conservative, pharmacological, and invasive therapies are provided. Conventional percutaneous transluminal angioplasty (PTA) using modern low-profile systems is associated with high technical success rates. However, initial data from recent randomized, controlled trials suggest that drug-eluting stents are consistently achieving improved patency over PTA alone or over bare metal stents. This review summarizes recent advances in the treatment of infrapopliteal disease.

  7. Disposable and removable nucleic acid extraction and purification cartridges for automated flow-through systems

    DOE Patents [OSTI]

    Regan, John Frederick

    2014-09-09T23:59:59.000Z

    Removable cartridges are used on automated flow-through systems for the purpose of extracting and purifying genetic material from complex matrices. Different types of cartridges are paired with specific automated protocols to concentrate, extract, and purifying pathogenic or human genetic material. Their flow-through nature allows large quantities sample to be processed. Matrices may be filtered using size exclusion and/or affinity filters to concentrate the pathogen of interest. Lysed material is ultimately passed through a filter to remove the insoluble material before the soluble genetic material is delivered past a silica-like membrane that binds the genetic material, where it is washed, dried, and eluted. Cartridges are inserted into the housing areas of flow-through automated instruments, which are equipped with sensors to ensure proper placement and usage of the cartridges. Properly inserted cartridges create fluid- and air-tight seals with the flow lines of an automated instrument.

  8. Biomedical silver-109m isotope generator

    DOE Patents [OSTI]

    Wanek, P.M.; Steinkruger, F.J.; Moody, D.C.

    1985-03-05T23:59:59.000Z

    A method, composition of matter, and apparatus for producing substantially pure Ag-109m for use in biomedical imaging techniques. Cd-109, which decays with a half-life of 453 days to Ag-109m, is loaded onto an ion exchange column consisting of particulate tin phosphate. After secular equilibrium is reached in about ten minutes, Ag-109m may be selectively eluted from the column by means of a physiologically acceptable aqueous buffered eluent solution of sodium thiosulfate, and either ascorbic acid or dextrose. The breakthrough of toxic Cd-109 is on the order of 1 x 10-7, which is sufficiently low to permit administration of the Ag-109m-containing eluate, with but a minor pH adjustment, directly to a human patient within a matter of seconds. 1 fig.

  9. Biomedical silver-109m isotope generator

    DOE Patents [OSTI]

    Wanek, Philip M. (Los Alamos, NM); Steinkruger, Frederick J. (Los Alamos, NM); Moody, David C. (Los Alamos, NM)

    1987-01-01T23:59:59.000Z

    A method, composition of matter, and apparatus for producing substantially pure Ag-109m for use in biomedical imaging techniques. Cd-109, which decays with a half-life of 453 days to Ag-109m is loaded onto an ion exchange column consisting of particulate tin phosphate. After secular equilibrium is reached in about ten minutes, Ag-109m may be selectively eluted from the column by means of a physiologically acceptable aqueous buffered eluent solution of sodium thiosulfate, and either ascorbic acid or dextrose. The breakthrough of toxic Cd-109 is on the order of 1.times.10.sup.-7, which is sufficiently low to permit administration of the Ag-109m-containing eluate, with but a minor pH adjustment, directly to a human patient within a matter of seconds.

  10. Modeling of thermal processes in very high pressure liquid chromatography for column immersed in a water bath: Application of the selected models

    SciTech Connect (OSTI)

    Gritti, Fabrice [University of Tennessee, Knoxville (UTK); Guiochon, Georges A [ORNL; Kaczmarski, Krzysztof [University of Tennessee and Rzeszow University of Technology, Poland

    2010-01-01T23:59:59.000Z

    Currently, chromatographic analyses are carried out by operating columns packed with sub-2 {micro}m particles under very high pressure gradients, up to 1200 bar for 5 cm long columns. This provides the high flow rates that are necessary for the achievement of high column efficiencies and short analysis times. However, operating columns at high flow rates under such high pressure gradients generate a large amount of heat due to the viscous friction of the mobile phase stream that percolates through a low permeability bed. The evacuation of this heat causes the formation of significant or even large axial and radial gradients of all the physico-chemical parameters characterizing the packing material and the mobile phase, eventually resulting in a loss of column efficiency. We previously developed and successfully applied a model combining the heat and the mass balances of a chromatographic column operated under very high pressure gradients (VHPLC). The use of this model requires accurate estimates of the dispersion coefficients at each applied mobile phase velocity. This work reports on a modification of the mass balance model such that only one measurement is now necessary to accurately predict elution peak profiles in a wide range of mobile phase velocities. The conditions under which the simple equilibrium-dispersive (ED) and transport-dispersive (TD) models are applicable in VHPLC are also discussed. This work proves that the new combination of the heat transfer and the ED model discussed in this work enables the calculation of accurate profiles for peaks eluted under extreme conditions, like when the column is thermostated in a water bath.

  11. Partial purification from macrophages of a phospholipase A/sub 2/ that hydrolyzes arachidonic acid from phosphatidylcholine

    SciTech Connect (OSTI)

    Leslie, C.; Wall, M.; Zelarney, P.; Voelker, D.

    1987-05-01T23:59:59.000Z

    The first step in platelet-activating factor production and arachidonic acid release from stimulated inflammatory cells is thought to be the activation of a phospholipase A/sub 2/ (PLA/sub 2/). The mouse macrophage cell line, RAW 264, was found to contain PLA/sub 2/ activity that hydrolyzed /sup 3/H-arachidonic acid from sonicated dispersions of 1-0-alkyl-linked phosphatidylcholine (PC). The PLA/sub 2/ was cytosolic, required calcium, and exhibited a broad pH optimum between 6 and 10. When the hydrolysis of /sup 3/H-arachidonic acid from 1-palmitoyl- and 1-hexadecyl-linked PC (15 ..mu..M) was compared, slightly higher activity against 1-acyl-linked PC was found. However, the activity against 1-palmitoyl-linked PC substrates containing oleic or linoleic acids (sn-2) was considerably lower. To understand the properties of the PLA/sub 2/ in more detail, purification was undertaken. After ammonium sulfate precipitation the PLA/sub 2/ was fractionated over G150, on which it eluted slightly before an albumin marker. The enzyme bound to DEAE cellulose at pH 8.0 and was eluted in 0.3M NaCl. Further purification was achieved by hydrophobic chromatography over phenyl Sepharose followed by ion-exchange chromatography using Q-Sepharose resulting in 200-700-fold increases in specific activity. These results demonstrate the presence of a cytosolic PLA/sub 2/ in macrophages that shows specificity for arachidonic acid at the sn-2 position of PC, has an apparent molecular weight greater than or equal to albumin, is anionic at pH 8.0 and is relatively hydrophobic.

  12. ACTIVATION OF A PEPTIDERGIC SYNAPSE LOCALLY MODULATES POSTSYNAPTIC CALCIUM INFLUX

    E-Print Network [OSTI]

    J. E. Richmond; L. R. Funte; W. L. Smith; D. A. Price; P. G. Haydon

    1991-01-01T23:59:59.000Z

    We examined the synaptic connection between Phe-Met-Arg-Phe-NH2 (FMRFamide)-immunoreactive neurone VD4 and its target neurone PI, both found in the central nervous system of the pond snail Helisoma trivolvis. The major FMRFamide-like peak in neurone VD4 appears to be FMRFamide itself, based on its high performance liquid chromatography (HPLC) elution time and immunoreactivity before and after oxidation, but small peaks are also present at the elution times of Phe-Leu-Arg-Phe-NH2 (FLRFamide) and Gly-Asp-Pro-Phe-Leu-Arg-Phe-NH2 (GDPFLRFamide). The modulatory actions of the neuropeptides found in neurone VD4 were tested on the postsynaptic target cell PI. Bath application of both the tetrapep-tides FMRFamide and FLRFamide at a concentration of 10~5 mol I"1 reduced the macroscopic voltage-sensitive calcium current of neurone PI in culture; FMRF-amide by 45 % and FLRFamide by 51 %. Bath application of the heptapeptide GDPFLRFamide (10~5 mol \\~l) reduced the calcium current by only 8 %. We reconstructed the synaptic connection between VD4 and PI in culture. Action-potential-evoked calcium transients in neurites growing from PI cells in culture were monitored using Fura-2. Addition of FMRFamide, FLRFamide or GDPFLRFamide reduced the magnitude of the calcium transient in PI. Stimu-lation of VD4 mimicked the effects of peptide application and caused localized reductions in the action-potential-evoked calcium transients in PI at the points of contact between the neurites of neurones VD4 and PI. These results suggest that neurone VD4 modulates the calcium influx of neurone PI through the release of endogenous FMRFamide-related peptides and that this modulatory action is restricted to sites of synaptic interaction.

  13. Rhenium-188: Availability from the W-188/Re-188 Generator and Status of Current Applications

    SciTech Connect (OSTI)

    Pillai, M R A [Bhabha Atomic Research Centre, Mumbai, India; Dash, A [Bhabha Atomic Research Centre, Mumbai, India; Knapp Jr, Russ F [ORNL

    2012-01-01T23:59:59.000Z

    Rhenium-188 is one of the most readily available generator derived and useful radionuclides for therapy emitting - particles (2.12 MeV, 71.1% and 1.965 MeV, 25.6%) and imageable gammas (155 KeV, 15.1%). The 188W/188Re generator is an ideal source for the long term (4-6 months) continuous availability of no carrier added (nca) 188Re suitable for the preparation of radiopharmaceuticals for radionuclide therapy. The challenges associated with the double neutron capture route of production of the parent 188W radionuclide have been a major impediment in the progress of application of 188Re. Tungsten-188 of adequate specific activity can be prepared only in 2-3 of the high flux reactors operating in the World. Several useful technologies have been developed for the preparation of clinical grade 188W/188Re generator. Since the specific activity of 188W used in the generator is relatively low (<5 Ci/g), the eluted 188ReO4- can have low radioactive concentration often insufficient for radiopharmaceutical preparation. However, several efficient post elution concentration techniques have been developed that yield clinically useful 188ReO4-. Rhenium-188 has been used for the preparation of therapeutic radiopharmaceuticals for the management of diseases such as bone metastasis, rheumatoid arthritis and primary cancers. Several early phase clinical studies using radiopharmaceuticals based on 188Re-labeled phosphonates, antibodies, peptides, lipiodol and particulates have been reported. This article reviews the availability, and use of188Re including a discussion of why broader use of 188Re has not progressed as ecpected as a popular radionuclide for therapy.

  14. Alkaline flooding injection strategy

    SciTech Connect (OSTI)

    French, T.R.; Josephson, C.B.

    1992-03-01T23:59:59.000Z

    The objective of this project is to improved alkali-surfactant flooding methods, and this includes determining the proper design of injection strategy. Several different injection strategies have been used or suggested for recovering heavy oils with surfactant-enhanced alkaline flooding methods. Oil recovery was compared for four different injection strategies: (1) surfactant followed by polymer, (2) surfactant followed by alkaline polymer, (3) alkaline surfactant followed by polymer, and (4) alkali, surfactant, and polymer mixed in a single formulation. The effect of alkaline preflush was also studied under two different conditions. All of the oil recovery experiments were conducted under optimal conditions with a viscous, non-acidic oil from Hepler (KS) oil field. The coreflood experiments were conducted with Berea sandstone cores since field core was not available in sufficient quantity for coreflood tests. The Tucker sand of Hepler field is a Class I fluvial dominated deltaic reservoir, as classified by the Department of Energy, which has been selected as the site of a DOE-sponsored field pilot test.

  15. LITERATURE REVIEWS TO SUPPORT ION EXCHANGE TECHNOLOGY SELECTION FOR MODULAR SALT PROCESSING

    SciTech Connect (OSTI)

    King, W

    2007-11-30T23:59:59.000Z

    This report summarizes the results of literature reviews conducted to support the selection of a cesium removal technology for application in a small column ion exchange (SCIX) unit supported within a high level waste tank. SCIX is being considered as a technology for the treatment of radioactive salt solutions in order to accelerate closure of waste tanks at the Savannah River Site (SRS) as part of the Modular Salt Processing (MSP) technology development program. Two ion exchange materials, spherical Resorcinol-Formaldehyde (RF) and engineered Crystalline Silicotitanate (CST), are being considered for use within the SCIX unit. Both ion exchange materials have been studied extensively and are known to have high affinities for cesium ions in caustic tank waste supernates. RF is an elutable organic resin and CST is a non-elutable inorganic material. Waste treatment processes developed for the two technologies will differ with regard to solutions processed, secondary waste streams generated, optimum column size, and waste throughput. Pertinent references, anticipated processing sequences for utilization in waste treatment, gaps in the available data, and technical comparisons will be provided for the two ion exchange materials to assist in technology selection for SCIX. The engineered, granular form of CST (UOP IE-911) was the baseline ion exchange material used for the initial development and design of the SRS SCIX process (McCabe, 2005). To date, in-tank SCIX has not been implemented for treatment of radioactive waste solutions at SRS. Since initial development and consideration of SCIX for SRS waste treatment an alternative technology has been developed as part of the River Protection Project Waste Treatment Plant (RPP-WTP) Research and Technology program (Thorson, 2006). Spherical RF resin is the baseline media for cesium removal in the RPP-WTP, which was designed for the treatment of radioactive waste supernates and is currently under construction in Hanford, WA. Application of RF for cesium removal in the Hanford WTP does not involve in-riser columns but does utilize the resin in large scale column configurations in a waste treatment facility. The basic conceptual design for SCIX involves the dissolution of saltcake in SRS Tanks 1-3 to give approximately 6 M sodium solutions and the treatment of these solutions for cesium removal using one or two columns supported within a high level waste tank. Prior to ion exchange treatment, the solutions will be filtered for removal of entrained solids. In addition to Tanks 1-3, solutions in two other tanks (37 and 41) will require treatment for cesium removal in the SCIX unit. The previous SCIX design (McCabe, 2005) utilized CST for cesium removal with downflow supernate processing and included a CST grinder following cesium loading. Grinding of CST was necessary to make the cesium-loaded material suitable for vitrification in the SRS Defense Waste Processing Facility (DWPF). Because RF resin is elutable (and reusable) and processing requires conversion between sodium and hydrogen forms using caustic and acidic solutions more liquid processing steps are involved. The WTP baseline process involves a series of caustic and acidic solutions (downflow processing) with water washes between pH transitions across neutral. In addition, due to resin swelling during conversion from hydrogen to sodium form an upflow caustic regeneration step is required. Presumably, one of these basic processes (or some variation) will be utilized for MSP for the appropriate ion exchange technology selected. CST processing involves two primary waste products: loaded CST and decontaminated salt solution (DSS). RF processing involves three primary waste products: spent RF resin, DSS, and acidic cesium eluate, although the resin is reusable and typically does not require replacement until completion of multiple treatment cycles. CST processing requires grinding of the ion exchange media, handling of solids with high cesium loading, and handling of liquid wash and conditioning solutions. RF processing requires h

  16. In-Source Fragmentation and the Sources of Partially Tryptic Peptides in Shotgun Proteomics

    SciTech Connect (OSTI)

    Kim, Jong Seo; Monroe, Matthew E.; Camp, David G.; Smith, Richard D.; Qian, Weijun

    2013-02-01T23:59:59.000Z

    Partially tryptic peptides are often identified in shotgun proteomics using trypsin as the proteolytic enzyme; however, it has been controversial regarding the sources of such partially tryptic peptides. Herein we investigate the impact of in-source fragmentation on shotgun proteomics using three biological samples, including a standard protein mixture, a mouse brain tissue homogenate, and a mouse plasma sample. Since the in-source fragments of a peptide retain the same elution time with its parent fully tryptic peptide, the partially tryptic peptides from in-source fragmentation can be distinguished from the other partially tryptic peptides by plotting the observed retention times against the computationally predicted retention times. Most partially tryptic in-source fragmentation artifacts were misaligned from the linear distribution of fully tryptic peptides. The impact of in-source fragmentation on peptide identifications was clearly significant in a less complex sample such as a standard protein digest, where ~60 % of unique peptides were observed as partially tryptic peptides from in-source fragmentation. In mouse brain or mouse plasma samples, in-source fragmentation contributed to 1-3 % of all identified peptides. The other major source of partially tryptic peptides in complex biological samples is presumably proteolytic processing by endogenous proteases in the samples. By filtering out the in-source fragmentation artifacts from the identified partially tryptic or non-tryptic peptides, it is possible to directly survey in-vivo proteolytic processing in biological samples such as blood plasma. ?

  17. Effect of force-induced mechanical stress at the coronary artery bifurcation stenting: Relation to in-stent restenosis

    SciTech Connect (OSTI)

    Lee, Cheng-Hung [Division of Cardiology, Department of Internal Medicine, Chang Gung Memorial Hospital, Linkou, Chang Gung University College of Medicine, Tao-Yuan, Taiwan (China); Department of Mechanical Engineering, Chang Gung University, Tao-Yuan, Taiwan (China); Jhong, Guan-Heng [Graduate Institute of Medical Mechatronics, Chang Gung University, Tao-Yuan, Taiwan (China); Hsu, Ming-Yi; Wang, Chao-Jan [Department of Medical Imaging and Intervention, Chang Gung Memorial Hospital, Linkou, Tao-Yuan, Taiwan (China); Liu, Shih-Jung, E-mail: shihjung@mail.cgu.edu.tw [Department of Mechanical Engineering, Chang Gung University, Tao-Yuan, Taiwan (China); Hung, Kuo-Chun [Division of Cardiology, Department of Internal Medicine, Chang Gung Memorial Hospital, Linkou, Chang Gung University College of Medicine, Tao-Yuan, Taiwan (China)

    2014-05-28T23:59:59.000Z

    The deployment of metallic stents during percutaneous coronary intervention has become common in the treatment of coronary bifurcation lesions. However, restenosis occurs mostly at the bifurcation area even in present era of drug-eluting stents. To achieve adequate deployment, physicians may unintentionally apply force to the strut of the stents through balloon, guiding catheters, or other devices. This force may deform the struts and impose excessive mechanical stresses on the arterial vessels, resulting in detrimental outcomes. This study investigated the relationship between the distribution of stress in a stent and bifurcation angle using finite element analysis. The unintentionally applied force following stent implantation was measured using a force sensor that was made in the laboratory. Geometrical information on the coronary arteries of 11 subjects was extracted from contrast-enhanced computed tomography scan data. The numerical results reveal that the application of force by physicians generated significantly higher mechanical stresses in the arterial bifurcation than in the proximal and distal parts of the stent (post hoc P?

  18. Literature Review of Spherical Resorcinol-Formaldehyde for Cesium Ion Exchange

    SciTech Connect (OSTI)

    Brown, Garrett N.

    2014-09-30T23:59:59.000Z

    The current report summarizes work performed throughout the scientific community and DOE complex as reported in the open literature and DOE-sponsored reports to evaluate the Cs+ ion exchange (CIX) characteristics of SRF resin. King (2007) completed a similar literature review in support of material selection for the Small Column Ion Exchange (SCIX) project. Josephson et al. (2010) and Sams et al. (2009) provided a similar brief review of SRF CIX for the near-tank Cs+ removal (NTCR) project. Thorson (2008a) documented the basis for recommending SRF over SuperLigTM 644 as the primary CIX resin in the WTP. The current review expands on previous work, summarizes additional work completed to date, and provides a broad view of the literature without focusing on a specific column system. Although the focus of the current review is the SRF resin, many cited references include multiple materials such as the non-spherical GGRF and SuperLigTM 644 organic resins and crystalline silicotitanate (CST) IONSIVTM IE-911, a non-elutable inorganic material. This report summarizes relevant information provided in the literature.

  19. Fabrication and In Vitro Deployment of a Laser-Activated Shape Memory Polymer Vascular Stent

    SciTech Connect (OSTI)

    Baer, G M; Small IV, W; Wilson, T S; Benett, W J; Matthews, D L; Hartman, J; Maitland, D J

    2007-04-25T23:59:59.000Z

    Vascular stents are small tubular scaffolds used in the treatment of arterial stenosis (narrowing of the vessel). Most vascular stents are metallic and are deployed either by balloon expansion or by self-expansion. A shape memory polymer (SMP) stent may enhance flexibility, compliance, and drug elution compared to its current metallic counterparts. The purpose of this study was to describe the fabrication of a laser-activated SMP stent and demonstrate photothermal expansion of the stent in an in vitro artery model. A novel SMP stent was fabricated from thermoplastic polyurethane. A solid SMP tube formed by dip coating a stainless steel pin was laser-etched to create the mesh pattern of the finished stent. The stent was crimped over a fiber-optic cylindrical light diffuser coupled to an infrared diode laser. Photothermal actuation of the stent was performed in a water-filled mock artery. At a physiological flow rate, the stent did not fully expand at the maximum laser power (8.6 W) due to convective cooling. However, under zero flow, simulating the technique of endovascular flow occlusion, complete laser actuation was achieved in the mock artery at a laser power of {approx}8 W. We have shown the design and fabrication of an SMP stent and a means of light delivery for photothermal actuation. Though further studies are required to optimize the device and assess thermal tissue damage, photothermal actuation of the SMP stent was demonstrated.

  20. Aromatic measurements of diesel fuel - A CRC round-robin study

    SciTech Connect (OSTI)

    Seizinger, D.E.; Hoekman, S.K.

    1984-01-01T23:59:59.000Z

    A round robin study to measure the aromatic levels in diesel fuels was conducted by the Chemical Characterization Panel of the Coordinating Research Council Air Pollution Research Advisory Committee (CRC-APRAC) In-house Program Group, CAPI-1-64. The fuels for this study consisted of a jet fuel, a No. 2 diesel reference fuel, and three fuels used in a CRC-sponsored diesel emission project (CAPE-32). These fuels had 90% distillation temperatures which ranged from 472/sup 0/ to 642/sup 0/ F and aromaticity levels from approximately 18 to 55% by volume. All participants used the American Society for Testing and Materials (ASTM) D1319 or modified D1319 methods to measure the aromatic levels in the selected fuels. Some participants concurrently analyzed the same fuels using other methods such as high-performance liquid chromatography, mass spectrometry, nuclear magnetic resonance spectrometry, and elution chromatography (ASTM D2549). One non-participating laboratory analyzed the fuels using supercritical fluid chromatography. The results of nine participants using the D1319 methodology and other methods showed good agreement for fuels with 90% distillation temperatures less than 600/sup 0/ F. However, this round robin study showed that: 1) there is no standard method to measure aromatic levels in full boiling range diesel fuels, and 2) there are inadequacies when using the D1319 and modified D1319 methods for fuels outside of the specified property ranges.

  1. Reversed-phase liquid chromatography of radiolabeled peptides using a C18 guard-PAK precolumn system

    SciTech Connect (OSTI)

    Carriere, P.D.; Bennett, H.P. (McGill Univ., Montreal, Quebec (Canada))

    1989-03-01T23:59:59.000Z

    In order to avoid radioactive contamination of high-performance liquid chromatography columns and injectors, we have investigated the use of a Guard-PAK precolumn system for the chromatography of ({sup 125}I) labeled peptides. Two gonadotropin-releasing hormone analogs: (1) (D-Ala6-des-Gly10)-GnRH (GnRH-(Ala6)) and (2) (D-Ser(TBu)6-des-Gly10)-GnRH (GnRH-(Ser6)) and rat prolactin (r-PRL) were radiolabeled with {sup 125}I and subjected to reversed-phase liquid chromatography using a C18 Guard-PAK precolumn system. Major peak fractions of purified ({sup 125}I)GnRH-(Ala6), ({sup 125}I)GnRH-(Ser6), and ({sup 125}I)r-PRL eluted at 24%, 28%, and 55% acetonitrile, respectively. Purified ({sup 125}I)GnRH analogs showed specific high affinity binding to rat anterior pituitary gland membranes (specific activity: 1500-1700 Ci/mmol). Purified ({sup 125}I)r-PRL showed high affinity binding to r-PRL antibody by RIA (specific activity: 70-75 microCi/micrograms). This rapid and efficient chromatographic method should be useful in the separation of a wide range of radiolabeled protein and peptide molecules.

  2. Nuclear medicine program progress report for quarter ending March 31, 1991

    SciTech Connect (OSTI)

    Knapp, F.F. Jr.; Ambrose, K.R.; Callahan, A.P.; McPherson, D.W.; Mirzadeh, S.; Srivastava, P.C.; Allred, J.F.; Hasan, A.; Lambert, C.R.; Lambert, S.J.; Rice, D.E.

    1991-08-01T23:59:59.000Z

    In this report the first fabrication and evaluation of an activated carbon-based osmium-194/iridium-194 generator system is described. Iridium-194 (t{sub {1/2}} = 19.2 h) decays by {Beta}{sup {minus}} emission (E{sub max} = 2.24 MeV) and is a potential candidate for radioimmunotherapy. An important characteristic is availability of {sup 194}Ir from decay of reactor-produced {sup 194}Os (t{sub {1/2}} = 6 y). A novel gas thermochromatographic method was developed for the one step conversion of metallic Os to OsO{sub 4} and subsequent separation and purification of OsO{sub 4}, which was then converted to the K{sub 2}OsCl{sub 6} for generator loading. The yield and the elution profile of carrier-free {sup 194}Ir, and {sup 194}Os breakthrough were determined for a prototype generator which was evaluated over a 10 month-period.l During this period several agents were also supplied to Medical Cooperative investigators, including iodine-123-labelled and iodine-125-labelled fatty acid analogues for studies at the Brookhaven National Laboratory. In addition, gold-198 and tungsten-188/-rhenium-188 generators were shipped to various investigators for therapeutic studies involving tumor-specific antibodies. 19 refs., 3 figs.

  3. MODELING RESULTS FROM CESIUM ION EXCHANGE PROCESSING WITH SPHERICAL RESINS

    SciTech Connect (OSTI)

    Nash, C.; Hang, T.; Aleman, S.

    2011-01-03T23:59:59.000Z

    Ion exchange modeling was conducted at the Savannah River National Laboratory to compare the performance of two organic resins in support of Small Column Ion Exchange (SCIX). In-tank ion exchange (IX) columns are being considered for cesium removal at Hanford and the Savannah River Site (SRS). The spherical forms of resorcinol formaldehyde ion exchange resin (sRF) as well as a hypothetical spherical SuperLig{reg_sign} 644 (SL644) are evaluated for decontamination of dissolved saltcake wastes (supernates). Both SuperLig{reg_sign} and resorcinol formaldehyde resin beds can exhibit hydraulic problems in their granular (nonspherical) forms. SRS waste is generally lower in potassium and organic components than Hanford waste. Using VERSE-LC Version 7.8 along with the cesium Freundlich/Langmuir isotherms to simulate the waste decontamination in ion exchange columns, spherical SL644 was found to reduce column cycling by 50% for high-potassium supernates, but sRF performed equally well for the lowest-potassium feeds. Reduced cycling results in reduction of nitric acid (resin elution) and sodium addition (resin regeneration), therefore, significantly reducing life-cycle operational costs. These findings motivate the development of a spherical form of SL644. This work demonstrates the versatility of the ion exchange modeling to study the effects of resin characteristics on processing cycles, rates, and cold chemical consumption. The value of a resin with increased selectivity for cesium over potassium can be assessed for further development.

  4. Analysis of interaction partners of H4 histone by a new proteomics approach

    E-Print Network [OSTI]

    Evelyne Saade; Undine Mechold; Arman Kulyyassov; Damien Vertut; Marc Lipinski; Vasily Ogryzko

    2009-10-30T23:59:59.000Z

    We describe a modification of the TAP method for purification and analysis of multiprotein complexes, termed here DEF-TAP (for Differential Elution Fractionation after Tandem Affinity Purification). Its essential new feature is the use for last purification step of 6XHis-Ni++ interaction, which is resistant to a variety of harsh washing conditions, including high ionic strength and presence of organic solvents. This allows us to use various fractionation schemes before the protease digestion, which is expected to improve the coverage of the analysed protein mixture and also to provide an additional insight into the structure of the purified macromolecular complex and the nature of protein-protein interactions involved. We illustrate our new approach by analysis of soluble nuclear complexes containing histone H4 purified from HeLa cells. In particular, we observed different fractionation patterns of HAT1 and RbAp46 proteins as compared to RbAp48 protein, all identified as interaction partners of H4 histone. In addition, we report all components of the licensing MCM2-7 complex and the apoptosis-related DAXX protein among the interaction partners of the soluble H4. Finally, we show that HAT1 requires N-terminal tail of H4 for its stable association with this histone.

  5. Continuous countercurrent chromatographic separator for the purification of sugars from biomass hydrolyzate. Final project report, July 1, 1996--September 30, 1997

    SciTech Connect (OSTI)

    Wooley, R.J.

    1997-12-01T23:59:59.000Z

    Production of pure sugars is required to enable production of fuels and chemicals from biomass feedstocks. Hydrolysis of cellulose and hemicellulose (principal constituents of biomass) produces sugars that can be utilized in various fermentation process to produce valuable chemicals. Unfortunately, the hydrolysis process also liberates chemicals from the biomass that can be toxic to the fermenting organisms. The two primary toxic components of biomass hydrolyzate are sulfuric acid (catalyst used in the hydrolysis) and acetic acid (a component of the feed biomass). In the standard batch chromatographic separation of these three components, sugar elutes in the middle. Batch chromatographic separations are not practical on a commercial scale, because of excess dilution and high capital costs. Because sugar is the {open_quotes}center product,{close_quotes} a continuous separation would require two costly binary separators. However, a single, slightly larger separator, configured to produce three products, would be more economical. This FIRST project develops a cost-effective method for purifying biomass hydrolyzate into fermentable sugars using a single continuous countercurrent separator to separate this ternary mixture.

  6. Ultratrace detector for hand-held gas chromatography

    DOE Patents [OSTI]

    Andresen, Brian D. (Livermore, CA); Miller, Fred S. (Bethal Island, CA)

    1999-01-01T23:59:59.000Z

    An ultratrace detector system for hand-held gas chromatography having high sensitivity, for example, to emissions generated during production of weapons, biological compounds, drugs, etc. The detector system is insensitive to water, air, helium, argon, oxygen, and C0.sub.2. The detector system is basically composed of a hand-held capillary gas chromatography (GC), an insulated heated redox-chamber, a detection chamber, and a vapor trap. For example, the detector system may use gas phase redox reactions and spectral absorption of mercury vapor. The gas chromatograph initially separates compounds that percolate through a bed of heated mercuric oxide (HgO) in a silica--or other metal--aerogel material which acts as an insulator. Compounds easily oxidized by HgO liberate atomic mercury that subsequently pass through a detection chamber which includes a detector cell, such as quartz, that is illuminated with a 254 nm ultra-violet (UV) mercury discharge lamp which generates the exact mercury absorption bands that are used to detect the liberated mercury atoms. Atomic mercury strongly absorbs 254 nm energy is therefore a specific signal for reducing compounds eluting from the capillary GC, whereafter the atomic mercury is trapped for example, in a silicon-aerogel trap.

  7. Method for detection of extremely low concentration

    DOE Patents [OSTI]

    Andresen, Brian D. (Livermore, CA); Miller, Fred S. (Bethal Island, CA)

    2002-01-01T23:59:59.000Z

    An ultratrace detector system for hand-held gas chromatography having high sensitivity, for example, to emissions generated during production of weapons, biological compounds, drugs, etc. The detector system is insensitive to water, air, helium, argon, oxygen, and CO.sub.2. The detector system is basically composed of a hand-held capillary gas chromatography (GC), an insulated heated redox-chamber, a detection chamber, and a vapor trap. For example, the detector system may use gas phase redox reactions and spectral absorption of mercury vapor. The gas chromatograph initially separates compounds that percolate through a bed of heated mercuric oxide (HgO) in a silica--or other metal--aerogel material which acts as an insulator. Compounds easily oxidized by HgO liberate atomic mercury that subsequently pass through a detection chamber which includes a detector cell, such as quartz, that is illuminated with a 254 nm ultra-violet (UV) mercury discharge lamp which generates the exact mercury absorption bands that are used to detect the liberated mercury atoms. Atomic mercury strongly absorbs 254 nm energy is therefore a specific signal for reducing compounds eluting from the capillary GC, whereafter the atomic mercury is trapped for example, in a silicon-aerogel trap.

  8. Molecular Size and Weight of Asphaltene and Asphaltene Solubility Fractions from Coals, Crude Oils and Bitumen

    SciTech Connect (OSTI)

    Badre,S.; Goncalves, C.; Norinaga, K.; Gustavson, G.; Mullins, O.

    2005-01-01T23:59:59.000Z

    The molecular weight of asphaltenes has been a controversy for several decades. In recent years, several techniques have converged on the size of the fused ring system; indicating that chromophores in virgin crude oil asphaltenes typically have 4-10 fused rings. Consequently, the molecular weight debate is equivalent to determining whether asphaltenes are monomeric (one fused-ring system per molecule) or whether they are polymeric. Time-resolved fluorescence depolarization (FD) is employed here to interrogate the absolute size of asphaltene molecules and to determine the relation of the size of the fused ring system to that of the corresponding molecule. Coal, petroleum and bitumen asphaltenes are compared. Molecular size of coal asphaltenes obtained here by FD-determined rotational diffusion match closely with Taylor-dispersion-derived translational diffusion measurements with UV absorption. Coal asphaltenes are smaller than petroleum asphaltenes. N-methyl pyrrolidinone (NMP) soluble and insoluble fractions are examined. NMP soluble and insoluble fractions of asphaltenes are monomeric. It is suggested that the 'giant' asphaltene molecules reported from SEC studies using NMP as the eluting solvent may actually be the expected flocs of asphaltene which are not soluble in NMP. Data is presented that intramolecular electronic relaxation in asphaltenes does not perturb FD results.

  9. Producing a True Lignin Depolymerase for Biobleaching Softwood Kraft Pulp

    SciTech Connect (OSTI)

    Simo Sarkanen

    2002-02-04T23:59:59.000Z

    This project constituted an intensive effort devoted to producing, from the white-rot fungus Tramets Cingulata, a lignin degrading enzyme (lignin depolymerase) that is directly able to biobleach or delignify softwood kraft pulp brownstock. To this end, the solutions in which T. cingulata was grown contained dissolved kraft lignin which fulfilled two functions; it behaved as a lignin deploymerase substrate and it also appeared to act as an inducer of enzyme expression. However, the lignin depolymerase isoenzymes (and other extracellular T. cingulata enzymes) interacted very strongly with both the kraft lignin components and the fungal hypae, so the isolating these proteins from the culture solutions proved to be unexpectedly difficult. Even after extensive experimentation with a variety of protein purification techniques, only one approach appeared to be capable of purifying lignin depolymerases to homogeneity. Unfortunately the procedure was extremely laborious; it involved the iso electric focusing of concentrated buffer-exchanged culture solutions followed by electro-elution of the desired protein bands from the appropriate polyacrylamide gel segments

  10. Fire Safety Tests for Spherical Resorcinol Formaldehyde Resin: Data Summary Report

    SciTech Connect (OSTI)

    Kim, Dong-Sang; Peterson, Reid A.; Schweiger, Michael J.

    2012-07-30T23:59:59.000Z

    A draft safety evaluation of the scenario for spherical resorcinol-formaldehyde (SRF) resin fire inside the ion exchange column was performed by the Hanford Tank Waste Treatment and Immobilization Plant (WTP) Fire Safety organization. The result of this draft evaluation suggested a potential change of the fire safety classification for the Cesium Ion Exchange Process System (CXP) emergency elution vessels, equipment, and piping, which may be overly bounding based on the fire performance data from the manufacturer of the ion exchange resin selected for use at the WTP. To resolve this question, the fire properties of the SRF resin were measured by Southwest Research Institute (SwRI), following the American Society for Testing and Materials (ASTM) standard procedures, through a subcontract managed by Pacific Northwest National Laboratory (PNNL). For some tests, the ASTM standard procedures were not entirely appropriate or practical for the SRF resin material, so the procedures were modified and deviations from the ASTM standard procedures were noted. This report summarizes the results of fire safety tests performed and reported by SwRI. The efforts by PNNL were limited to summarizing the test results provided by SwRI into one consolidated data report. All as-received SwRI reports are attached to this report in the Appendix. Where applicable, the precision and bias of each test method, as given by each ASTM standard procedure, are included and compared with the SwRI test results of the SRF resin.

  11. Recent International R&D Activities in the Extraction of Uranium from Seawater

    SciTech Connect (OSTI)

    Rao, Linfeng

    2010-03-15T23:59:59.000Z

    A literature survey has been conducted to collect information on the International R&D activities in the extraction of uranium from seawater for the period from the 1960s till the year of 2010. The reported activities, on both the laboratory scale bench experiments and the large scale marine experiments, were summarized by country/region in this report. Among all countries where such activities have been reported, Japan has carried out the most advanced large scale marine experiments with the amidoxime-based system, and achieved the collection efficiency (1.5 g-U/kg-adsorbent for 30 days soaking in the ocean) that could justify the development of industrial scale marine systems to produce uranium from seawater at the price competitive with those from conventional uranium resources. R&D opportunities are discussed for improving the system performance (selectivity for uranium, loading capacity, chemical stability and mechanical durability in the sorption-elution cycle, and sorption kinetics) and making the collection of uranium from seawater more economically competitive.

  12. Effect on Intimal Hyperplasia of Dexamethasone Released from Coated Metal Stents Compared with Non-Coated Stents in Canine Femoral Arteries

    SciTech Connect (OSTI)

    Strecker, Ernst-Peter [Department of Radiology, Diakonissen-Hospital, Diakonissenstrasse 28, D-76199 Karlsruhe (Germany); Gabelmann, Andreas [Department of Radiology, University Hospital, Hugstetter Strasse 55, D-79106 Freiburg (Germany); Boos, Irene [Department of Radiology, Diakonissen-Hospital, Diakonissenstrasse 28, D-76199 Karlsruhe (Germany); Lucas, Christopher [Department of Pharmaceutical Technology and Biopharmacy, University Heidelberg, Im Neuenheimer Feld 366, D-69120 Heidelberg (Germany); Xu, Zhongying [Department of Radiology, Diakonissen-Hospital, Diakonissenstrasse 28, D-76199 Karlsruhe (Germany); Haberstroh, Joerg [Department of Surgical Research, University Hospital, Breisacher Strasse 64, D-79108 Freiburg (Germany); Freudenberg, Nicolaus [Department of Pathology, University Hospital, Albertstrasse 19, D-79002 Freiburg (Germany); Stricker, Helmut [Department of Pharmaceutical Technology and Biopharmacy, University Heidelberg, Im Neuenheimer Feld 366, D-69120 Heidelberg (Germany); Langer, Mathias [Department of Radiology, University Hospital, Hugstetter Strasse 55, D-79106 Freiburg (Germany); Betz, Eberhard [Department of Physiology, University Tuebingen, Gmelinstrasse 5, D-72076 Tuebingen (Germany)

    1998-11-15T23:59:59.000Z

    Purpose: Polymer-coated, dexamethasone (DXM)-releasing stents were tested in order to assess the efficacy of DXM released locally for the prevention of stent restenosis due to intimal hyperplasia. Methods: Strecker stents coated with a biodegradable membrane containing DXM were implanted percutaneously into the femoral artery in 14 dogs. The contralateral artery received a conventional non-coated stent serving as control. The drugs are eluted by degradation of the carrier membrane. Follow-up intraarterial digital subtraction angiography (DSA) was obtained at 3, 6, 9, 12, and 24 weeks with subsequent autopsy. Specimens for gross and microscopic pathology were obtained and histomorphometry was performed. Results: Four of 14 DXM-coated stents showed thrombotic occlusion within the first 3 weeks; ten DXM-coated stents remained patent. At follow-up DSA, DXM-coated stents showed a significantly wider lumen than the non-coated stents. At morphometry there was less intimal hyperplasia over DXM-coated stents than over non-coated stents (p < 0.05). Conclusion: DXM-coated stents reduce neointimal hyperplasia in dogs when compared with non-coated stents.

  13. HIGH ASPECT RATIO ION EXCHANGE RESIN BED - HYDRAULIC RESULTS FOR SPERICAL RESIN BEADS

    SciTech Connect (OSTI)

    Duignan, M; Charles Nash, C; Timothy Punch, T

    2007-09-27T23:59:59.000Z

    A principal role of the DOE Savannah River Site is to safely dispose of a large volume of liquid nuclear waste held in many storage tanks. An in-tank ion exchange unit is being considered for cesium removal to accelerate waste processing. This unit is planned to have a relatively high bed height to diameter ratio (10:1). Complicating the design is the need to cool the ion exchange media; therefore, the ion exchange column will have a central cooling core making the flow path annular. To separate cesium from waste the media being considered is made of resorcinol formaldehyde resin deposited on spherical plastic beads and is a substitute for a previously tested resin made of crystalline silicotitanate. This spherical media not only has an advantage of being mechanically robust, but, unlike its predecessor, it is also reusable, that is, loaded cesium can be removed through elution and regeneration. Resin regeneration leads to more efficient operation and less spent resin waste, but its hydraulic performance in the planned ion exchange column was unknown. Moreover, the recycling process of this spherical resorcinol formaldehyde causes its volume to significantly shrink and swell. To determine the spherical media's hydraulic demand a linearly scaled column was designed and tested. The waste simulant used was prototypic of the wastes' viscosity and density. This paper discusses the hydraulic performance of the media that will be used to assist in the design of a full-scale unit.

  14. Site Selection for the Salt Disposition Facility at the Savannah River Site

    SciTech Connect (OSTI)

    Gladden, J.B.; Rueter, K.J.; Morin, J.P.

    2000-11-15T23:59:59.000Z

    A site selection study was conducted to identify a suitable location for the construction and operation of a new Salt Disposition Facility (SDF) at the Savannah River Site (SRS). The facility to be sited is a single processing facility and support buildings that could house either of three technology alternatives being developed by the High Level Waste Systems Engineering Team: Small Tank Tetraphenylborate Precipitation, Crystalline Silicotitanate Non-Elutable Ion Exchange or Caustic Side Solvent Extraction. A fourth alternative, Direct Disposal in grout, is not part of the site selection study because a location has been identified that is unique to this technology (i.e., Z-Area). Facility site selection at SRS is a formal, documented process that seeks to optimize siting of new facilities with respect to facility-specific engineering requirements, sensitive environmental resources, and applicable regulatory requirements. In this manner, the prime objectives of cost minimization, environmental protection, and regulatory compliance are achieved. The results from this geotechnical characterization indicated that continued consideration be given to Site B for the proposed SDF. Suitable topography, the lack of surface hydrology and floodplain issues, no significant groundwater contamination, the presence of minor soft zones along the northeast portion of footprint, and no apparent geological structure in the Gordon Aquitard support this recommendation.

  15. Method for selective recovery of PET-usable quantities of [.sup.18 F] fluoride and [.sup.13 N] nitrate/nitrite from a single irradiation of low-enriched [.sup.18 O] water

    DOE Patents [OSTI]

    Ferrieri, Richard A. (Patchogue, NY); Schlyer, David J. (Bellport, NY); Shea, Colleen (Wading River, NY)

    1995-06-13T23:59:59.000Z

    A process for simultaneously producing PET-usable quantities of [.sup.13 N]NH.sub.3 and [.sup.18 F]F.sup.- for radiotracer synthesis is disclosed. The process includes producing [.sup.13 N]NO.sub.2.sup.- /NO.sub.3.sup.- and [.sup.18 F]F.sup.- simultaneously by exposing a low-enriched (20%-30%) [.sup.18 O]H.sub.2 O target to proton irradiation, sequentially isolating the [.sup.13 N]NO.sub.2.sup.- /NO.sub.3.sup.- and [.sup.18 F]F.sup.- from the [.sup.18 O]H.sub.2 O target, and reducing the [.sup.13 N]NO.sub.2.sup.- /NO.sub.3.sup.- to [.sup.13 N]NH.sub.3. The [.sup.13 N]NH.sub.3 and [.sup.18 F]F.sup.- products are then conveyed to a laboratory for radiotracer applications. The process employs an anion exchange resin for isolation of the isotopes from the [.sup.18 O]H.sub.2 O, and sequential elution of [.sup.13 N]NO.sub.2.sup.- /NO.sub.3.sup.- and [ .sup.18 F]F.sup.- fractions. Also the apparatus is disclosed for simultaneously producing PET-usable quantities of [.sup.13 N]NH.sub.3 and [.sup.18 F]F.sup.- from a single irradiation of a single low-enriched [.sup.18 O]H.sub.2 O target.

  16. Spiral wound extraction cartridge

    DOE Patents [OSTI]

    Wisted, Eric E. (Apple Valley, MN); Lundquist, Susan H. (White Bear Township, MN)

    1999-01-01T23:59:59.000Z

    A cartridge device for removing an analyte from a fluid comprises a hollow core, a sheet composite comprising a particulate-loaded porous membrane and optionally at least one reinforcing spacer sheet, the particulate being capable of binding the analyte, the sheet composite being formed into a spiral configuration about the core, wherein the sheet composite is wound around itself and wherein the windings of sheet composite are of sufficient tightness so that adjacent layers are essentially free of spaces therebetween, two end caps which are disposed over the core and the lateral ends of the spirally wound sheet composite, and means for securing the end caps to the core, the end caps also being secured to the lateral ends of the spirally wound sheet composite. A method for removing an analyte from a fluid comprises the steps of providing a spirally wound element of the invention and passing the fluid containing the analyte through the element essentially normal to a surface of the sheet composite so as to bind the analyte to the particulate of the particulate-loaded porous membrane, the method optionally including the step of eluting the bound analyte from the sheet composite.

  17. Plutonium scrap processing at the Los Alamos Scientific Laboratory

    SciTech Connect (OSTI)

    Nixon, A.E.; McKerley, B.J.; Christensen, E.L.

    1980-01-01T23:59:59.000Z

    The Los Alamos Scientific Laboratory currently has the newest plutonium handling facility in the nation. Los Alamos has been active in the processing of plutonium almost since the discovery of this man-made element in 1941. One of the functions of the new facility is the processing of plutonium scrap generated at LASL and other sites. The feed for the scrap processing program is extremely varied, and a wide variety of contaminants are often encountered. Depending upon the scrap matrix and contaminants present, the majority of material receives a nitric acid/hydrofluoric acid or nitric acid/calcium fluoride leach. The plutonium nitrate solutions are then loaded onto an anion exchange column charged with DOWEX 1 x 4, 50 to 100 mesh, nitrate form resin. The column is eluted with 0.48 M hydroxyl amine nitrate. The Pu(NO/sub 3/)/sub 3/ is then precipitated as plutonium III oxalate which is calcined at 450 to 500/sup 0/C to yield a purified PuO/sub 2/ product.

  18. The New Element Californium (Atomic Number 98)

    DOE R&D Accomplishments [OSTI]

    Seaborg, G. T.; Thompson, S. G.; Street, K. Jr.; Ghiroso, A.

    1950-06-19T23:59:59.000Z

    Definite identification has been made of an isotope of the element with atomic number 98 through the irradiation of Cm{sup 242} with about 35-Mev helium ions in the Berkeley Crocker Laboratory 60-inch cyclotron. The isotope which has been identified has an observed half-life of about 45 minutes and is thought to have the mass number 244. The observed mode of decay of 98{sup 244} is through the emission of alpha-particles, with energy of about 7.1 Mev, which agrees with predictions. Other considerations involving the systematics of radioactivity in this region indicate that it should also be unstable toward decay by electron capture. The chemical separation and identification of the new element was accomplished through the use of ion exchange adsorption methods employing the resin Dowex-50. The element 98 isotope appears in the eka-dysprosium position on elution curves containing berkelium and curium as reference points--that is, it precedes berkelium and curium off the column in like manner that dysprosium precedes terbium and gadolinium. The experiments so far have revealed only the tripositive oxidation state of eka-dysprosium character and suggest either that higher oxidation states are not stable in aqueous solutions or that the rates of oxidation are slow. The successful identification of so small an amount of an isotope of element 98 was possible only through having made accurate predictions of the chemical and radioactive properties.

  19. Method and apparatus for selective filtering of ions

    DOE Patents [OSTI]

    Page, Jason S. (Kennewick, WA); Tang, Keqi (Richland, WA); Smith, Richard D. (Richland, WA)

    2009-04-07T23:59:59.000Z

    An adjustable, low mass-to-charge (m/z) filter is disclosed employing electrospray ionization to block ions associated with unwanted low m/z species from entering the mass spectrometer and contributing their space charge to down-stream ion accumulation steps. The low-mass filter is made by using an adjustable potential energy barrier from the conductance limiting terminal electrode of an electrodynamic ion funnel, which prohibits species with higher ion mobilities from being transmitted. The filter provides a linear voltage adjustment of low-mass filtering from m/z values from about 50 to about 500. Mass filtering above m/z 500 can also be performed; however, higher m/z species are attenuated. The mass filter was evaluated with a liquid chromatography-mass spectrometry analysis of an albumin tryptic digest and resulted in the ability to block low-mass, "background" ions which account for 40-70% of the total ion current from the ESI source during peak elution.

  20. The Role of Interventional Radiology in the Diagnosis and Management of Male Impotence

    SciTech Connect (OSTI)

    Spiliopoulos, Stavros [Patras University Hospital, Department of Radiology (Greece)] [Patras University Hospital, Department of Radiology (Greece); Shaida, Nadeem [Cambridge University Hospitals NHS Trust, Addenbrooke's University Hospital, Department of Radiology (United Kingdom)] [Cambridge University Hospitals NHS Trust, Addenbrooke's University Hospital, Department of Radiology (United Kingdom); Katsanos, Konstantinos [Guy's and St Thomas' NHS Trust, Department of Radiology (United Kingdom)] [Guy's and St Thomas' NHS Trust, Department of Radiology (United Kingdom); Krokidis, Miltiadis, E-mail: mkrokidis@hotmail.com [Cambridge University Hospitals NHS Trust, Addenbrooke's University Hospital, Department of Radiology (United Kingdom)] [Cambridge University Hospitals NHS Trust, Addenbrooke's University Hospital, Department of Radiology (United Kingdom)

    2013-10-15T23:59:59.000Z

    Erectile dysfunction (ED) is defined as the persistent inability to reach or maintain penile rigidity enough for sexual satisfaction. Nearly 30% of the men between ages 40 and 70 years are affected by ED. A variety of pathologies, including neurological, psychological, or endocrine disorders and drug side effects, may incite ED. A commonly identified cause of ED is vascular disease. Initial diagnostic workup includes a detailed physical examination and laboratory tests. Whilst duplex ultrasound is considered the first-line diagnostic modality, intra-arterial digital subtraction angiography is still considered the 'gold standard' for the diagnosis of arteriogenic impotence. Percutaneous endovascular treatment may be offered in patients with vasculogenic ED that has failed to respond to oral medical therapy as an alternative to penile prosthesis or open surgical repair. In arteriogenic ED balloon angioplasty of the aorto-iliac axis, and in veno-occlusive ED, percutaneous venous ablation using various embolization materials has been reported to be safe and to improve sexual performance. Recently, the ZEN study investigated the safety and feasibility of drug-eluting stents for the treatment of arteriogenic ED attributed to internal pudendal artery stenosis with promising preliminary results. This manuscript highlights the role of interventional radiology in the diagnosis and minimally invasive treatment of male impotence.

  1. Four methods for determining the composition of trace radioactive surface contamination of low-radioactivity metal

    E-Print Network [OSTI]

    O'Keeffe, H M; Cleveland, B T; Doucas, G; Gagnon, N; Jelley, N A; Kraus, C; Lawson, I T; Majerus, S; McGee, S R; Myers, A W; Poon, A W P; Rielage, K; Robertson, R G H; Rosten, R C; Stonehill, L C; VanDevender, B A; Van Wechel, T D

    2011-01-01T23:59:59.000Z

    Four methods for determining the composition of low-level uranium- and thorium-chain surface contamination are presented. One method is the observation of Cherenkov light production in water. In two additional methods a position-sensitive proportional counter surrounding the surface is used to make both a measurement of the energy spectrum of alpha particle emissions and also coincidence measurements to derive the thorium-chain content based on the presence of short-lived isotopes in that decay chain. The fourth method is a radiochemical technique in which the surface is eluted with a weak acid, the eluate is concentrated, added to liquid scintillator and assayed by recording beta-alpha coincidences. These methods were used to characterize two `hotspots' on the outer surface of one of the He-3 proportional counters in the Neutral Current Detection array of the Sudbury Neutrino Observatory experiment. The methods have similar sensitivities, of order tens of ng, to both thorium- and uranium-chain contamination.

  2. Four methods for determining the composition of trace radioactive surface contamination of low-radioactivity metal

    E-Print Network [OSTI]

    H. M. O'Keeffe; T. H. Burritt; B. T. Cleveland; G. Doucas; N. Gagnon; N. A. Jelley; C. Kraus; I. T. Lawson; S. Majerus; S. R. McGee; A. W. Myers; A. W. P. Poon; K. Rielage; R. G. H. Robertson; R. C. Rosten; L. C. Stonehill; B. A. VanDevender; T. D. Van Wechel

    2011-03-29T23:59:59.000Z

    Four methods for determining the composition of low-level uranium- and thorium-chain surface contamination are presented. One method is the observation of Cherenkov light production in water. In two additional methods a position-sensitive proportional counter surrounding the surface is used to make both a measurement of the energy spectrum of alpha particle emissions and also coincidence measurements to derive the thorium-chain content based on the presence of short-lived isotopes in that decay chain. The fourth method is a radiochemical technique in which the surface is eluted with a weak acid, the eluate is concentrated, added to liquid scintillator and assayed by recording beta-alpha coincidences. These methods were used to characterize two `hotspots' on the outer surface of one of the He-3 proportional counters in the Neutral Current Detection array of the Sudbury Neutrino Observatory experiment. The methods have similar sensitivities, of order tens of ng, to both thorium- and uranium-chain contamination.

  3. Development of a high-throughput microfluidic integrated microarray for the detection of chimeric bioweapons.

    SciTech Connect (OSTI)

    Sheppod, Timothy; Satterfield, Brent; Hukari, Kyle W.; West, Jason A. A.; Hux, Gary A.

    2006-10-01T23:59:59.000Z

    The advancement of DNA cloning has significantly augmented the potential threat of a focused bioweapon assault, such as a terrorist attack. With current DNA cloning techniques, toxin genes from the most dangerous (but environmentally labile) bacterial or viral organism can now be selected and inserted into robust organism to produce an infinite number of deadly chimeric bioweapons. In order to neutralize such a threat, accurate detection of the expressed toxin genes, rather than classification on strain or genealogical decent of these organisms, is critical. The development of a high-throughput microarray approach will enable the detection of unknowns chimeric bioweapons. The development of a high-throughput microarray approach will enable the detection of unknown bioweapons. We have developed a unique microfluidic approach to capture and concentrate these threat genes (mRNA's) upto a 30 fold concentration. These captured oligonucleotides can then be used to synthesize in situ oligonucleotide copies (cDNA probes) of the captured genes. An integrated microfluidic architecture will enable us to control flows of reagents, perform clean-up steps and finally elute nanoliter volumes of synthesized oligonucleotides probes. The integrated approach has enabled a process where chimeric or conventional bioweapons can rapidly be identified based on their toxic function, rather than being restricted to information that may not identify the critical nature of the threat.

  4. Rapid separation and purification of uranium and plutonium from dilute-matrix samples

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Armstrong, Christopher R.; Ticknor, Brian W.; Hall, Gregory; Cadieux, James R.

    2014-03-11T23:59:59.000Z

    This work presents a streamlined separation and purification approach for trace uranium and plutonium from dilute (carrier-free) matrices. The method, effective for nanogram quantities of U and femtogram to picogram quantities of Pu, is ideally suited for environmental swipe samples that contain a small amount of collected bulk material. As such, it may be applicable for processing swipe samples such as those collected in IAEA inspection activities as well as swipes that are loaded with unknown analytes, such as those implemented in interlaboratory round-robin or proficiency tests. Additionally, the simplified actinide separation could find use in internal laboratory monitoring of clean room conditions prior to or following more extensive chemical processing. We describe key modifications to conventional techniques that result in a relatively rapid, cost-effective, and efficient U and Pu separation process. We demonstrate the efficacy of implementing anion exchange chromatography in a single column approach. We also show that hydrobromic acid is an effective substitute in lieu of hydroiodoic acid for eluting Pu. Lastly, we show that nitric acid is an effective digestion agent in lieu of perchloric acid and/or hydrofluoric acid. A step by step procedure of this process is detailed.

  5. Detailed analyses of FCC decant oil as a starting feedstock for mesophase pitch

    SciTech Connect (OSTI)

    Mochida, I.; Korai, Y.; Hieida, T. (Inst. of Advanced Material Study, Kyushu Univ. 86, Kasuga, Fukuoka 816 (JP)); Azuma, A.; Kitajima, E. (Osaka Research Lab., Koa Oil Co. Ltd., Takaishi-shi Osaka 592 (JP))

    1991-01-01T23:59:59.000Z

    Four typical DOs supplied from Japanese refineries were analyzed in detail by GC, FD-MS {sup 1}H and {sup 13}C-NMR after the fractionations by column chromatography. A DO carries 30% saturate and 70% aromatic fractions. The saturate consisted principally of the straight paraffins. The aromatic fraction was separated into five substractions (AR1 - AR5) of which contents distributed rather evenly, the middle fraction (AR 3) occupying the largest of 30%. The aromatic components had consisted of aromatic rings from 2(AR1) to 4(AR4+5), of some aryl-aryl linkages and naphthenic rings being included. The lighter aromatic fraction carried more alkyl groups, enhance its solubility and elution in the column. B DO appeared heaviest among the DOs in the present study. The oils carried only 10% of the saturate and 75% of AR3-AR5 aromatic subfractions. Its saturate was of carried rather short chains and more isoparaffins. Its aromatic components had very similar aromatic units to those of A DO in the same subfraction, although the heaviest fraction of the former once contained also a small portion of 6 aromatic rings.

  6. Perch population assessment in lakes reclaimed using oil-sands derived material

    SciTech Connect (OSTI)

    Heuvel, M.R. van den; Dixon, D.G. [Univ. of Waterloo, Ontario (Canada); Power, M. [Univ. of Manitoba, Winnipeg, Manitoba (Canada); Boerger, H.; MacKinnon, M.D.; Meer, T. van [Syncrude Canada, Fort McMurray, Alberta (Canada)

    1995-12-31T23:59:59.000Z

    The mining and extraction of petroleum products from oil-sands involves large areas of land and produces enormous volumes of tailings. One possible land reclamation option is to incorporate fine-tailings material into the bottoms of constructed lakes capped with natural surface water. The wet landscape method represents potential risk to aquatic biota-naphthenic acids and PAHs elute from pore water contained in the fine-tailings substrate. In spring 1995 yellow perch were stocked into a large-scale (5ha) experimental pond that consisted of fine-tailings capped with natural water as well as into two other reclaimed ponds that were constructed with oil-sands overburden material. Prior to stocking of perch, ponds had colonized with cyprinids, macrophytes and benthic invertebrates over a two year period. Perch were sampled in fall 1995 for age, condition factor, liver size, gonad size, fecundity, stomach contents, liver mixed-function oxygenase activity (MFO), bile PAH metabolites and plasma steroid hormones. When compared to the source lake, perch in the DP did not show reduced reproductive potential. Perch in all of the reclaimed ponds demonstrated exposure to organic compounds as indicated by marginally induced MFO activity and increased liver size. Exposure to naphthenates and PAHs in water as well as ecological environmental factors will be discussed.

  7. Membrane associated phospholipase C from bovine brain

    SciTech Connect (OSTI)

    Lee, K.; Ryu, S.H.; Suh, P.; Choi, W.C.; Rhee, S.G.

    1987-05-01T23:59:59.000Z

    Cytosolic fractions of bovine brain contain 2 immunologically distinct phosphoinositide-specific phospholipase (PLC), PLC-I and PLC-II, whose MW are 150,000 and 145,000 respectively, under a denaturing condition. Monoclonal antibodies were derived against each form and specific radioimmunoassays were developed. Distribution of PLC-I and PLC-II in cytosolic and particulate fractions was measured using the radioimmunoassay. More than 90% of PLC-II was found in the cytosolic fraction, while the anti-PLC-I antibody cross-reacting protein was distributed nearly equally between the soluble fraction and the 2 M KCl extract of particulate fraction. The PLC enzyme in the particulate fraction was purified to homogeneity, yielding 2 proteins of 140 KDa and 150 KDa when analyzed on SDS-PAGE. Neither of the 2 enzymes cross-reacted with anti-PLC-II antibodies, but both could be immunoblotted by all 4 different anti-PLC-I antibodies. This suggests that the 140 KDa PLC was derived from the 150 KDa form. The 150 Kda form from particulate fraction was indistinguishable from the cytosolic PLC-I when their mixture was analyzed on SDS-PAGE. In addition, the elution profile of tryptic peptides derived from the 150 KDa particulate form was identical to that of cytosolic PLC-I. This result indicates that PLC-I is reversibly associated to membranes.

  8. Photosensitization of human leukemic cells by anthracenedione antitumor agents

    SciTech Connect (OSTI)

    Hartley, J.A.; Forrow, S.M.; Souhami, R.L.; Reszka, K.; Lown, J.W. (University College and Middlesex School of Medicine, London (England))

    1990-03-15T23:59:59.000Z

    1,4-Diamino-substituted anthraquinone antitumor agents (mitoxantrone and ametantrone) and structurally related 1,5- and 1,8-diamino-substituted compounds (AM1 and AM2) were tested for their ability to photosensitize human leukemic cells in culture. Viability was measured using the 3,4,5-dimethylthiazol-2,5-diphenyl tetrazolium bromide assay, and DNA and membrane damage were assessed. Following a 1-h exposure to AM2, a dose of drug required to give 50% loss of cell viability (53 microM) was obtained in the dark, which was reduced to approximately 2.4 microM following illumination for 2 min (lambda greater than 475 nm), a dose of light that was completely nontoxic to the cells in the absence of drug. A shift in the cell viability curve was also observed for AM1 but, under identical conditions, the dose modification was only 8.9. In contrast, neither ametantrone nor mitoxantrone gave a decreased viability upon illumination. DNA single-strand breaks as measured by alkaline elution correlated with cell viability. Frank DNA single-strand breaks were produced by AM2 and light, suggesting the production of free radicals. The strand breaks produced by AM2 in the dark and by mitoxantrone (with or without illumination) were protein concealed. No evidence of photo-induced membrane damage, as determined by transport of the model amino acid cycloleucine, could be observed even at supralethal doses.

  9. Separation Of Uranium And Plutonium Isotopes For Measurement By Multi Collector Inductively Coupled Plasma Mass Spectroscopy

    SciTech Connect (OSTI)

    Martinelli, R E; Hamilton, T F; Williams, R W; Kehl, S R

    2009-03-29T23:59:59.000Z

    Uranium (U) and plutonium (Pu) isotopes in coral soils, contaminated by nuclear weapons testing in the northern Marshall Islands, were isolated by ion-exchange chromatography and analyzed by mass spectrometry. The soil samples were spiked with {sup 233}U and {sup 242}Pu tracers, dissolved in minerals acids, and U and Pu isotopes isolated and purified on commercially available ion-exchange columns. The ion-exchange technique employed a TEVA{reg_sign} column coupled to a UTEVA{reg_sign} column. U and Pu isotope fractions were then further isolated using separate elution schemes, and the purified fractions containing U and Pu isotopes analyzed sequentially using multi-collector inductively coupled plasma mass spectrometer (MCICP-MS). High precision measurements of {sup 234}U/{sup 235}U, {sup 238}U/{sup 235}U, {sup 236}U/{sup 235}U, and {sup 240}Pu/{sup 239}Pu in soil samples were attained using the described methodology and instrumentation, and provide a basis for conducting more detailed assessments of the behavior and transfer of uranium and plutonium in the environment.

  10. Fire Safety Tests for Cesium-Loaded Spherical Resorcinol Formaldehyde Resin: Data Summary Report

    SciTech Connect (OSTI)

    Kim, Dong-Sang; Schweiger, Michael J.; Peterson, Reid A.

    2012-09-01T23:59:59.000Z

    A draft safety evaluation of the scenario for spherical resorcinol formaldehyde (SRF) resin fire inside the ion exchange column was performed by the Hanford Tank Waste Treatment and Immobilization Plant (WTP) Fire Safety organization. The result of this draft evaluation suggested a potential change of the fire safety classification for the Cesium Ion Exchange Process System (CXP) emergency elution vessels, equipment, and piping. To resolve this question, the fire properties of the SRF resin were measured by Southwest Research Institute (SwRI) through a subcontract managed by Pacific Northwest National Laboratory (PNNL). The results of initial fire safety tests on the SRF resin were documented in a previous report (WTP-RPT-218). The present report summarizes the results of additional tests performed by SwRI on the cesium-loaded SRF resin. The efforts by PNNL were limited to summarizing the test results provided by SwRI into one consolidated data report. The as-received SwRI report is attached to this report in the Appendix A. Where applicable, the precision and bias of each test method, as given by each American Society for Testing and Materials (ASTM) standard procedure, are included and compared with the SwRI test results of the cesium-loaded SRF resin.

  11. Adsorption of Ruthenium, Rhodium and Palladium from Simulated High-Level Liquid Waste by Highly Functional Xerogel - 13286

    SciTech Connect (OSTI)

    Onishi, Takashi [Fukushima Fuels and Materials Department O-arai Research and Development Center Japan Atomic Energy Agency, Narita-cho 4002, O-arai-machi, Ibaraki, 311-1393 (Japan)] [Fukushima Fuels and Materials Department O-arai Research and Development Center Japan Atomic Energy Agency, Narita-cho 4002, O-arai-machi, Ibaraki, 311-1393 (Japan); Koyama, Shin-ichi [Fukushima Fuels and Materials Department O-arai Research and Development Center Japan Atomic Energy Agency, Narita-cho 4002, O-arai-machi, Ibaraki, 311-1393 (Japan)] [Fukushima Fuels and Materials Department O-arai Research and Development Center Japan Atomic Energy Agency, Narita-cho 4002, O-arai-machi, Ibaraki, 311-1393 (Japan); Mimura, Hitoshi [Dept. of Quantum Science and Energy Engineering, Graduate School of Engineering, Tohoku University Aramaki-Aza-Aoba 6-6-01-2,Aoba-ku, Sendai-shi, Miyagi-ken, 980-8579 (Japan)] [Dept. of Quantum Science and Energy Engineering, Graduate School of Engineering, Tohoku University Aramaki-Aza-Aoba 6-6-01-2,Aoba-ku, Sendai-shi, Miyagi-ken, 980-8579 (Japan)

    2013-07-01T23:59:59.000Z

    Fission products are generated by fission reactions in nuclear fuel. Platinum group (Pt-G) elements, such as palladium (Pd), rhodium (Rh) and ruthenium (Ru), are also produced. Generally, Pt-G elements play important roles in chemical and electrical industries. Highly functional xerogels have been developed for recovery of these useful Pt-G elements from high - level radioactive liquid waste (HLLW). An adsorption experiment from simulated HLLW was done by the column method to study the selective adsorption of Pt-G elements, and it was found that not only Pd, Rh and Ru, but also nickel, zirconium and tellurium were adsorbed. All other elements were not adsorbed. Adsorbed Pd was recovered by washing the xerogel-packed column with thiourea solution and thiourea - nitric acid mixed solution in an elution experiment. Thiourea can be a poison for automotive exhaust emission system catalysts, so it is necessary to consider its removal. Thermal decomposition and an acid digestion treatment were conducted to remove sulfur in the recovered Pd fraction. The relative content of sulfur to Pd was decreased from 858 to 0.02 after the treatment. These results will contribute to design of the Pt-G element separation system. (authors)

  12. ECONOMIC RECOVERY OF OIL TRAPPED AT FAN MARGINS USING HIGH ANGLE WELLS AND MULTIPLE HYDRAULIC FRACTURES

    SciTech Connect (OSTI)

    Mike L. Laue

    2001-09-28T23:59:59.000Z

    This project attempts to demonstrate the effectiveness of exploiting thin-layered, low-energy deposits at the distal margin of a prograding turbidite complex through the use of hydraulically fractured horizontal or high-angle wells. The combination of a horizontal or high-angle well and hydraulic fracturing will allow greater pay exposure than can be achieved with conventional vertical wells while maintaining vertical communication between thin interbedded layers and the wellbore. A high-angle well will be drilled in the fan-margin portion of a slope-basin clastic reservoir and will be completed with multiple hydraulic-fracture treatments. Geologic modeling, reservoir characterization, and fine-grid reservoir simulation will be used to select the well location and orientation. Design parameters for the hydraulic-fracture treatments will be determined, in part, by fracturing an existing test well. Fracture azimuth will be predicted by passive seismic monitoring of a fracture-stimulation treatment in the test well using logging tools in an offset well. The long radius, near horizontal well was drilled during the first quarter of 1996. Well conditions resulted in the 7 in. production liner sticking approximately 900 ft off bottom. Therefore, a 5 in. production liner was necessary to case this portion of the target formation. Swept-out sand intervals and a poor cement bond behind the 5 in. liner precluded two of the three originally planned hydraulic fracture treatments. As a result, all pay intervals behind the 5 in. liner were perforated and stimulated with a non-acid reactive fluid. Following a short production period, the remaining pay intervals in the well (behind the 7 in. liner) were perforated. The well was returned to production to observe production trends and pressure behavior and assess the need to stimulate the new perforations.

  13. Spherical Resorcinol-Formaldehyde Synthesis by Inverse Suspension Polymerization

    SciTech Connect (OSTI)

    Ray, Robert J.; Scrivens, Walter A.; Nash, Charles

    2005-10-21T23:59:59.000Z

    Base catalyzed sol-gel polycondensation of resorcinol (1,3-dihydroxybenzene) with formaldehyde by inverse suspension polymerization leads to the formation of uniform, highly cross-linked, translucent, spherical gels, which have increased selectivity and capacity for cesium ion removal from high alkaline solutions. Because of its high selectivity for cesium ion, resorcinol-formaldehyde (R-F) resins are being considered for process scale column radioactive cesium removal by ion-exchange at the Waste Treatment and Immobilization Plant (WTP), which is now under construction at the Hanford site. Other specialty resins such as Superlig{reg_sign} 644 have been ground and sieved and column tested for process scale radioactive cesium removal but show high pressure drops across the resin bed during transition from column regeneration to loading and elution. Furthermore, van Deemter considerations indicate better displacement column chromatography by the use of spherical particle beads rather than irregularly shaped ground or granular particles. In our studies batch contact equilibrium experiments using a high alkaline simulant show a definite increase in cesium loading onto spherical R-F resin. Distribution coefficient (Kd) values ranged from 777 to 429 mL/g in the presence of 0.1M and 0.7M potassium ions, respectively. Though other techniques for making R-F resins have been employed, to our knowledge no one has made spherical R-F resins by inverse suspension polymerization. Moreover, in this study we discuss the data comparisons to known algebraic isotherms used to evaluate ion-exchange resins for WTP plant scale cesium removal operations.

  14. APPLICATION OF FORMOHYDROXAMIC ACID IN NUCLEAR PROCESSING: SYNTHESIS AND COMPLEXATION WITH TECHNETIUM-99

    SciTech Connect (OSTI)

    Amber Wright; Edward Mausolf; Keri Campbell; Frederic Poineau; P. Paviet-Hartmann

    2010-05-01T23:59:59.000Z

    Acetohydroxamic acid (AHA) is an organic ligand planned for use in the Uranium Extraction (UREX) process. It reduces neptunium and plutonium, and the resultant hydrophilic complexes are separated from uranium by extraction with tributyl phosphate (TBP) in a hydrocarbon diluent. AHA undergoes hydrolysis to acetic acid which will impede the recycling of nitric acid. During recent discussions of the UREX process, it has been proposed to replace AHA by formohydroxamic acid (FHA). FHA will undergo hydrolysis to formic acid which is volatile, thus allowing the recycling of nitric acid. The reported reduction potentials of AHA and pertechnetate (TcO{sub 4}{sup -}) indicated that it may be possible for AHA to reduce technetium, altering its fate in the fuel cycle. At UNLV, it has been demonstrated that TcO{sub 4}{sup -} undergoes reductive nitrosylation by AHA under a variety of conditions. The resulting divalent technetium is complexed by AHA to form the pseudo-octahedral trans-aquonitrosyl (diacetohydroxamic)-technetium(II) complex ([Tc{sup II}(NO)(AHA){sub 2}H{sub 2}O]{sup +}). In this paper, we are reporting the synthesis of FHA and its complex formation with technetium along with the characterization of FHA crystals achieved by NMR and IR spectroscopy. Two experiments were conducted to investigate the complexation of FHA with Tc and the results were compared with previous data on AHA. The first experiment involved the elution of Tc from a Reillex HP anion exchange resin, and the second one monitored the complexation of technetium with FHA by UV-visible spectrophotometry.

  15. Energy balance for uranium recovery from seawater

    SciTech Connect (OSTI)

    Schneider, E.; Lindner, H. [The University of Texas, 1 University Station C2200, Austin, TX 78712 (United States)

    2013-07-01T23:59:59.000Z

    The energy return on investment (EROI) of an energy resource is the ratio of the energy it ultimately produces to the energy used to recover it. EROI is a key viability measure for a new recovery technology, particularly in its early stages of development when financial cost assessment would be premature or highly uncertain. This paper estimates the EROI of uranium recovery from seawater via a braid adsorbent technology. In this paper, the energy cost of obtaining uranium from seawater is assessed by breaking the production chain into three processes: adsorbent production, adsorbent deployment and mooring, and uranium elution and purification. Both direct and embodied energy inputs are considered. Direct energy is the energy used by the processes themselves, while embodied energy is used to fabricate their material, equipment or chemical inputs. If the uranium is used in a once-through fuel cycle, the braid adsorbent technology EROI ranges from 12 to 27, depending on still-uncertain performance and system design parameters. It is highly sensitive to the adsorbent capacity in grams of U captured per kg of adsorbent as well as to potential economies in chemical use. This compares to an EROI of ca. 300 for contemporary terrestrial mining. It is important to note that these figures only consider the mineral extraction step in the fuel cycle. At a reference performance level of 2.76 g U recovered per kg adsorbent immersed, the largest energy consumers are the chemicals used in adsorbent production (63%), anchor chain mooring system fabrication and operations (17%), and unit processes in the adsorbent production step (12%). (authors)

  16. Removal of Pu238 from Neptunium Solution by Anion Exchange

    SciTech Connect (OSTI)

    KYSER, EDWARD

    2003-12-01T23:59:59.000Z

    A new anion flowsheet for use in HB-Line was tested in the lab with Reillex{trademark} HPQ for removal of Pu{sup 238} contamination from Np. Significant rejection of Pu{sup 238} was observed by washing with 6 to 12 bed volumes (BV) of reductive wash containing reduced nitric acid concentration along with both ferrous sulfamate (FS) and hydrazine. A shortened-height column was utilized in these tests to match changes in the plant equipment. Lab experiments scaled to plant batch sizes of 1500 to 2200 g Np were observed with modest losses for up-flow washing. Down-flow washing was observed to have high losses. The following are recommended conditions for removing Pu{sup 238} from Np solutions by anion exchange in HB-Line: (1) Feed conditions: Up-flow 6.4-8 M HNO{sub 3}, 0.02 M hydrazine, 0.05 M excess FS, less than 5 days storage of solution after FS addition. (2) Reductive Wash conditions: Up-flow 6-12 BV of 6.4 M HNO{sub 3}, 0.05 M FS, 0.05 M hydrazine. 1.8 mL/min/cm{sup 2} flowrate. (3) Decontamination Wash conditions: Up-flow 1-2 BV of 6.4-8 M HNO{sub 3}, no FS, no hydrazine. (4) Elution conditions: Down-flow 0.17 M HNO{sub 3}, 0.05 M hydrazine, no FS.

  17. Chemical and nuclear properties of lawrencium (element 103) and hahnium (element 105)

    SciTech Connect (OSTI)

    Henderson, R.A.

    1990-09-10T23:59:59.000Z

    The chemical and nuclear properties of Lr and Ha have been studied, using 3-minute {sup 260}Lr and 35-second {sup 262}Ha. The crystal ionic radius of Lr{sup 3+} was determined by comparing its elution position from a cation-exchange resin column with those of lanthanide elements having known ionic radii. Comparisons are made to the ionic radii of the heavy actinides, Am{sup 3+} through Es{sup 3+}, obtained by x-ray diffraction methods, and to Md{sup 3+} and Fm{sup 3+} which were determined in the same manner as Lr{sup 3+}. The hydration enthalpy of {minus}3622 kJ/mol was calculated from the crystal ionic radius using an empirical form of the Born equation. Comparisons to the spacings between the ionic radii of the heaviest members of the lanthanide series show that the 2Z spacing between Lr{sup 3+} and Md{sup 3+} is anomalously small, as the ionic radius of Lr{sup 3+} of 0.0886 nm is significantly smaller than had been expected. The chemical properties of Ha were determined relative to the lighter homologs in group 5, Nb and Ta. Group 4 and group 5 tracer activities, as well as Ha, were absorbed onto glass surfaces as a first step toward the determination of the chemical properties of Ha. Ha was found to adsorb on surfaces, a chemical property unique to the group 5 elements, and as such demonstrates that Ha has the chemical properties of a group 5 element. A solvent extraction procedure was adapted for use as a micro-scale chemical procedure to examine whether or not Ha displays eka-Ta-like chemical under conditions where Ta will be extracted into the organic phase and Nb will not. Under the conditions of this experiment Ha did not extract, and does not show eka-Ta-like chemical properties.

  18. Chronic graft-versus-host disease in the rat radiation chimera: I. clinical features, hematology, histology, and immunopathology in long-term chimeras

    SciTech Connect (OSTI)

    Beschorner, W.E.; Tutschka, P.J.; Santos, G.W.

    1982-04-01T23:59:59.000Z

    The clinical features, pathology, and immunopathology of chronic graft-versus-host disease (GVHD) developing in the long-term rat radiation chimera are described. At 6 to 12 months post-transplant, the previously stable ACI/LEW chimeras developed patchy to diffuse severe hair loss and thickened skin folds, and had microscopic features resembling scleroderma, Sjogren's syndrome, and chronic hepatitis. Skin histology showed dermal inflammation and acanthosis with atrophy of the appendages, with progression to dermal sclerosis. The liver revealed chronic hepatitis with bile duct injury and proliferation and periportal piecemeal necrosis. The tongue had considerable submucosal inflammation, muscular necrosis, and atrophy and arteritis. The serous salivary glands, lacrimal glands, and bronchi had lymphocytic inflammation and injury to duct, acinar, and mucosal columnar epithelium. The thymus had lymphocyte depletion of the medulla with prominent epithelium. The spleen and lymph nodes had poorly developed germinal centers but increased numbers of plasma cells. IgM was observed along the basement membrane and around the basal cells of the skin and tongue and along the basement membrane of the bile ducts. IgM was present also in the arteries of the tongue. Immunoglobulins eluted from the skin, cross-reacted with the bile duct epithelium and usually with both ACI and Lewis skin. Increased titers of speckled antinuclear antibodies were present in the serum of rats with chronic (GVHD). Chronic GVHD in the long-term rat radiation chimera is very similar to human chronic GVHD and is a potentially excellent model for autoimmune disorders including scleroderma, Sjorgren's syndrome, and chronic hepatitis.

  19. RAPID METHOD FOR DETERMINATION OF {sup 228}Ra IN WATER SAMPLES

    SciTech Connect (OSTI)

    Maxwell, S.

    2012-09-05T23:59:59.000Z

    A new rapid method for the determination of {sup 228}Ra in natural water samples has been developed at the SRNL/EBL (Savannah River National Lab/ Environmental Bioassay Laboratory) that can be used for emergency response or routine samples. While gamma spectrometry can be employed with sufficient detection limits to determine {sup 228}Ra in solid samples (via {sup 228}Ac) , radiochemical methods that employ gas flow proportional counting techniques typically provide lower MDA (Minimal Detectable Activity) levels for the determination of {sup 228}Ra in water samples. Most radiochemical methods for {sup 228}Ra collect and purify {sup 228}Ra and allow for {sup 228}Ac daughter ingrowth for ~36 hours. In this new SRNL/EBL approach, {sup 228}Ac is collected and purified from the water sample without waiting to eliminate this delay. The sample preparation requires only about 4 hours so that {sup 228}Ra assay results on water samples can be achieved in < 6 hours. The method uses a rapid calcium carbonate precipitation enhanced with a small amount of phosphate added to enhance chemical yields (typically >90%), followed by rapid cation exchange removal of calcium. Lead, bismuth, uranium, thorium and protactinium isotopes are also removed by the cation exchange separation. {sup 228}Ac is eluted from the cation resin directly onto a DGA Resin cartridge attached to the bottom of the cation column to purify {sup 228}Ac. DGA Resin also removes lead and bismuth isotopes, along with Sr isotopes and {sup 90}Y. La is used to determine {sup 228}Ac chemical yield via ICP-MS, but {sup 133}Ba can also be used instead if ICP-MS assay is not available. Unlike some older methods, no lead or strontium holdback carriers or continual readjustment of sample pH is required.

  20. Tyrosine hydroxylase is activated and phosphorylated at different sites in rat pheochromocytoma PC 12 cells treated with phorbol ester and forskolin

    SciTech Connect (OSTI)

    Tachikawa, E.; Tank, A.W.; Weiner, D.H.; Mosimann, W.F.; Yanagihara, N.; Weiner, N.

    1986-03-01T23:59:59.000Z

    The effects of phorbol ester (4..beta..-phorbol, 12..beta..-myristate, 13..cap alpha..-acetate; TPA), an activator of Ca/sup + +//phospholipid-dependent protein kinase (PK-C), and forskolin, which stimulates adenylate cyclase and cyclic AMP-dependent protein kinase (cAMP-PK), on the activation and phosphorylation of tyrosine hydroxylase (TH) in rat pheochromocytoma (PC 12) cells were examined. Incubation of the cells with TPA (0.01-1 ..mu..M) or forskolin (0.01-0.1 ..mu..M) produces increases in activation and phosphorylation of TH in a concentration-dependent manner. The stimulatory effects of TPA are dependent on extracellular Ca/sup + +/ and are inhibited by pretreatment of the cells with trifluoperazine (TFP). The effects of forskolin are independent of Ca/sup + +/ and are not inhibited by TFP. In cells treated with forskolin, the time course of the increase in cAMP correlates with the increases in TH activity and phosphorylation. cAMP levels do not increase in cells treated with TPA. There is an increase in the phosphorylation of only one tryptic phosphopeptide derived from TH in cells treated with either forskolin or TPA. The peptide phosphorylated in TPA-treated cells exhibits different elution characteristics on HPLC from that in forskolin-treated cells. The authors conclude that TH in PC 12 cells is phosphorylated on different sites by cAMP-PK and PK-C. Phosphorylation of either of these sites is associated with enzyme activation.

  1. The TGA codons are present in the open reading frame of selenoprotein P cDNA

    SciTech Connect (OSTI)

    Hill, K.E.; Lloyd, R.S.; Read, R.; Burk, R.F. (Vanderbilt Univ., Nashville, TN (United States))

    1991-03-11T23:59:59.000Z

    The TGA codon in DNA has been shown to direct incorporation of selenocysteine into protein. Several proteins from bacteria and animals contain selenocysteine in their primary structures. Each of the cDNA clones of these selenoproteins contains one TGA codon in the open reading frame which corresponds to the selenocysteine in the protein. A cDNA clone for selenoprotein P (SeP), obtained from a {gamma}ZAP rat liver library, was sequenced by the dideoxy termination method. The correct reading frame was determined by comparison of the deduced amino acid sequence with the amino acid sequence of several peptides from SeP. Using SeP labelled with {sup 75}Se in vivo, the selenocysteine content of the peptides was verified by the collection of carboxymethylated {sup 77}Se-selenocysteine as it eluted from the amino acid analyzer and determination of the radioactivity contained in the collected samples. Ten TGA codons are present in the open reading frame of the cDNA. Peptide fragmentation studies and the deduced sequence indicate that selenium-rich regions are located close to the carboxy terminus. Nine of the 10 selenocysteines are located in the terminal 26% of the sequence with four in the terminal 15 amino acids. The deduced sequence codes for a protein of 385 amino acids. Cleavage of the signal peptide gives the mature protein with 366 amino acids and a calculated mol wt of 41,052 Da. Searches of PIR and SWISSPROT protein databases revealed no similarity with glutathione peroxidase or other selenoproteins.

  2. Synthesis of octane enhancers during slurry-phase Fischer-Tropsch. Quarterly technical progress report No. 9, October 1, 1992--December 31, 1992

    SciTech Connect (OSTI)

    Marcelin, G.

    1993-06-30T23:59:59.000Z

    Figure 7 summarizes the carbon selectivities observed towards the main products. During Period IV, the main products observed were the heavy hydrocarbons, with selectivity for MTBE being less than 3--5%. The only time that high MTBE selectivity was noted was during period III, when the i-butylene feed was shut-off. The large amounts of heavy products and the low selectivity to MTBE were surprising in view of our previous experiments in the gas phase and the high methanol-to-i-butylene ratio used in these runs. In the gas-phase and with methanol/i-butylene = 0.5, over 95% selectivity to MTBE was observed with this catalyst at this temperature. The higher level of methanol used here would be expected to further improve the MTBE selectivity. Perhaps one reason for the poor MTBE selectivity relates to the relative solubilities of the reactants in the Synfluid changing the effective methanol/i-butylene ratio. Figure 8 shows the relative molar concentration of i-butylene during Period III. At 180 minutes, the gas supply of that reactant was shut-off, yet the analyses show that i-butylene continued to elute from the reactor for at least an additional 2 hours. It seems reasonable that the i-butylene is highly soluble in the Synfluid since they are both nonpolar hydrocarbons. Likewise, one would expect the methanol to not be quite as soluble and thus the methanol/i-butylene ratio in the liquid medium may be very low, favoring the oligomerization of i-butylene. Indeed, the only time that MTBE selectivity was high was after the i-butylene supply was shut-off. We intend to quantify these solubilities in future experiments.

  3. Method for selective recovery of PET-usable quantities of [{sup 18}F] fluoride and [{sup 13}N] nitrate/nitrite from a single irradiation of low-enriched [{sup 18}O] water

    DOE Patents [OSTI]

    Ferrieri, R.A.; Schlyer, D.J.; Shea, C.

    1995-06-13T23:59:59.000Z

    A process for simultaneously producing PET-usable quantities of [{sup 13}N]NH{sub 3} and [{sup 18}F]F{sup {minus}} for radiotracer synthesis is disclosed. The process includes producing [{sup 13}N]NO{sub 2}{sup {minus}}/NO{sub 3}{sup {minus}}and [{sup 18}F]F{sup {minus}} simultaneously by exposing a low-enriched (20%-30%) [{sup 18}O]H{sub 2}O target to proton irradiation, sequentially isolating the [{sup 13}N]NO{sub 2}{sup {minus}}/NO{sub 3}{sup {minus}} and [{sup 18}F]F{sup {minus}} from the [{sup 18}O]H{sub 2}O target, and reducing the [{sup 13}N]NO{sub 2}{sup {minus}}/NO{sub 3}{sup {minus}} to [{sup 13}N]NH{sub 3}. The [{sup 13}N]NH{sub 3} and [{sup 18}F]F{sup {minus}} products are then conveyed to a laboratory for radiotracer applications. The process employs an anion exchange resin for isolation of the isotopes from the [{sup 18}O]H{sub 2}O, and sequential elution of [{sup 13}N]NO{sub 2}{sup {minus}}/NO{sub 3}{sup {minus}} and [{sup 18}F]F{sup {minus}} fractions. Also the apparatus is disclosed for simultaneously producing PET-usable quantities of [{sup 13}N]NH{sub 3} and [{sup 18}F]F{sup {minus}} from a single irradiation of a single low-enriched [{sup 18}O]H{sub 2}O target. 2 figs.

  4. Separation of peptides from myoglobin enzymatic digests by RPLC. Influence of the mobile-phase composition and the pressure on the retention and separation

    SciTech Connect (OSTI)

    Marchetti, Nicola [University of Tennessee, Knoxville (UTK); Guiochon, Georges A [ORNL

    2005-06-01T23:59:59.000Z

    The influence of the mobile-phase composition and the pressure on the chromatographic separation of the peptides from the enzymatic digest of myoglobin was studied under linear conditions. The retention behavior of these tryptic peptides was measured under isocratic conditions with different mobile-phase compositions, ranging from 9 to 28% (v/v) acetonitrile in 0.1% (v/v) aqueous trifluoroacetic acid. The effect of the pressure was studied by analyzing the separation of the tryptic peptides under different average column pressures between 14 and 220 bar, at 13, 20, and 26% (v/v) acetonitrile. The differences between the partial molar volumes of these peptides in the stationary and mobile phases were derived from these results. All the measurements were performed on a 10-cm-long C{sub 18}-bonded, end-capped monolithic column. The results obtained illustrate the highly complicated behavior of the complex peptide mixtures afforded by tryptic digestion. The capacity factors of the analyzed peptides do not depend linearly on the acetonitrile concentration but follow exactly a quadratic relationship. The adsorption changes of partial molar volumes are in good agreement with other literature data. The consequences of the influence of the average column pressure (hence of the flow rate) on the column phase ratio and on the retention factors of the peptides are discussed. The retention pattern of the complex mixture is affected by both the mobile-phase composition and the pressure, and the resolution of certain peptide pairs is so much affected by the pressure that inversions in the elution order of some pairs are observed.

  5. Routine production of copper-64 using 11.7MeV protons

    SciTech Connect (OSTI)

    Jeffery, C. M.; Smith, S. V.; Asad, A. H.; Chan, S.; Price, R. I. [Medical Technology and Physics, Sir Charles Gairdner Hospital, Nedlands, Western Australia, 6009 (Australia); Centre for Forensic Science, University of Western Australia, Nedlands, Western Australia, 6009 (Australia) and ARC Centre of Excellence in A (Australia); ARC Centre of Excellence in Antimatter-Matter Studies, Australian National University, Canberra, ACT 0200 (Australia) and Collider-Accelerator Department, Brookhaven National Laboratory, Upton, NY 11973 (United States); Medical Technology and Physics, Sir Charles Gairdner Hospital, Nedlands, Western Australia, 6009 (Australia); ARC Centre of Excellence in Antimatter-Matter Studies, Australian National University, Canberra, ACT 0200 (Australia) and Imaging and Applied (Australia); Medical Technology and Physics, Sir Charles Gairdner Hospital, Nedlands, Western Australia, 6009 (Australia); Medical Technology and Physics, Sir Charles Gairdner Hospital, Nedlands, Western Australia, 6009 (Australia) and School of Physics, University of Western Australia, Nedlands, Western Australia, 6009 (Australia)

    2012-12-19T23:59:59.000Z

    Reliable production of copper-64 ({sup 64}Cu) was achieved by irradiating enriched nickel-64 ({sup 64}Ni, >94.8%) in an IBA 18/9 cyclotron. Nickel-64 (19.1 {+-} 3.0 mg) was electroplated onto an Au disc (125{mu}m Multiplication-Sign 15mm). Targets were irradiated with 11.7 MeV protons for 2 hours at 40{mu}A. Copper isotopes ({sup 60,61,62,64}Cu) were separated from target nickel and cobalt isotopes ({sup 55,57,61}Co) using a single ion exchange column, eluted with varying concentration of low HCl alcohol solutions. The {sup 64}Ni target material was recovered and reused. The {sup 64}Cu production rate was 1.46{+-}0.3MBq/{mu}A.hr/mg{sup 64}Ni(n = 10) (with a maximum of 2.6GBq of {sup 64}Cu isolated after 2hr irradiation at 40uA. Radionuclidic purity of the {sup 64}Cu was 98.7 {+-} 1.6 % at end of separation. Cu content was < 6mg/L (n = 21). The specific activity of {sup 64}Cu was determined by ICP-MS and by titration with Diamsar to be 28.9{+-}13.0GBq/{mu}mol[0.70{+-}0.35Ci/{mu}mol]/({mu}A.hr/mg{sup 64}Ni)(n = 10) and 13.1{+-}12.0GBq/{mu}mol[0.35{+-}0.32Ci/{mu}mol]/({mu}A.hr/mg{sup 64}Ni)(n 9), respectively; which are in agreement, however, further work is required.

  6. LITERATURE REVIEW FOR OXALATE OXIDATION PROCESSES AND PLUTONIUM OXALATE SOLUBILITY

    SciTech Connect (OSTI)

    Nash, C.

    2012-02-03T23:59:59.000Z

    A literature review of oxalate oxidation processes finds that manganese(II)-catalyzed nitric acid oxidation of oxalate in precipitate filtrate is a viable and well-documented process. The process has been operated on the large scale at Savannah River in the past, including oxidation of 20 tons of oxalic acid in F-Canyon. Research data under a variety of conditions show the process to be robust. This process is recommended for oxalate destruction in H-Canyon in the upcoming program to produce feed for the MOX facility. Prevention of plutonium oxalate precipitation in filtrate can be achieved by concentrated nitric acid/ferric nitrate sequestration of oxalate. Organic complexants do not appear practical to sequester plutonium. Testing is proposed to confirm the literature and calculation findings of this review at projected operating conditions for the upcoming campaign. H Canyon plans to commence conversion of plutonium metal to low-fired plutonium oxide in 2012 for eventual use in the Mixed Oxide Fuel (MOX) Facility. The flowsheet includes sequential operations of metal dissolution, ion exchange, elution, oxalate precipitation, filtration, and calcination. All processes beyond dissolution will occur in HB-Line. The filtration step produces an aqueous filtrate that may have as much as 4 M nitric acid and 0.15 M oxalate. The oxalate needs to be removed from the stream to prevent possible downstream precipitation of residual plutonium when the solution is processed in H Canyon. In addition, sending the oxalate to the waste tank farm is undesirable. This report addresses the processing options for destroying the oxalate in existing H Canyon equipment.

  7. Effect of Fe2+ Oxidation on the Removal of 238Pu from Neptunium Solution by Anion Exchange

    SciTech Connect (OSTI)

    KYSER, EDWARD

    2004-06-01T23:59:59.000Z

    The effect of ferrous sulfamate (FS) oxidation and variation in nitric acid concentration on the removal of {sup 238}Pu contamination from Np by the HB-Line anion exchange flowsheet has been tested. Significant rejection of {sup 238}Pu was observed by washing with a reductive wash solution containing 6.0 to 6.8 M nitric acid (HNO{sub 3}) with as little as 30% of the Fe{sup 2+} from the FS remaining in its reduced form. To achieve the desired 30% removal of {sup 238}Pu from the process, conditions should be controlled to maintain the Fe{sup 2+}/Fe{sup 3+} ratio in the reductive wash to be greater than 60%/40% (or 1.5). Since Fe{sup 2+} oxidation is strongly affected by temperature and nitric acid concentration, these parameters (as well as time after FS addition) need to be controlled to ensure predictable results. A shortened-height column was utilized in these tests to match changes in the plant equipment. Lab experiments scaled to plant batch sizes of 2000 g Np were observed with modest losses for ''up-flow'' washing. The following are recommended conditions for removing {sup 238}Pu from Np solutions by anion exchange in HB-Line: (1) Feed conditions: ''Up-flow'' 6.4-8.0 M HNO{sub 3}, 0.02 M hydrazine (N{sub 2}H{sub 4}), 0.05 M excess FS. (2) Reductive Wash conditions: ''Up-flow'' 6 Bed volumes (BV) of 6.4 M HNO{sub 3}, 0.05 M FS (minimum 0.03M Fe{sup 2+} during wash cycle), 0.05 M hydrazine, less than 1.8 mL/min/cm{sup 2} flowrate. (3) Decontamination Wash conditions: ''Up-flow'' 1-2 BV of 6.4-8.0 M HNO{sub 3}, no FS, no hydrazine, less than 1.8 mL/min/cm{sup 2} flowrate. (4) Elution conditions: ''Down-flow'' 0.17 M HNO{sub 3}, 0.05 M hydrazine, no FS.

  8. THERMAL ANALYSIS FOR IN-TANK ION-EXCHANGE COLUMN PROCESS

    SciTech Connect (OSTI)

    Lee, S; Frank02 Smith, F

    2009-01-05T23:59:59.000Z

    High Level Waste (HLW) at the Savannah River Site (SRS) is stored in three forms: sludge, saltcake, and supernate. A small column ion-exchange (SCIX) process is being designed to treat dissolved saltcake waste before feeding it to the saltstone facility to be made into grout. The waste is caustic with high concentrations of various sodium salts and lower concentrations of radionuclides. Two cation exchange media being considered are a granular form of crystalline silicotitanate (CST) and a spherical form of resorcinol-formaldehyde (RF) resin. CST is an inorganic material highly selective for cesium that is not elutable. Through this process, radioactive cesium from the salt solution is absorbed into ion exchange media (either CST or RF) which is packed within a flow-through column. A packed column loaded with radioactive cesium generates significant heat from radiolytic decay. If engineering designs cannot handle this thermal load, hot spots may develop locally which could degrade the performance of the ion-exchange media. Performance degradation with regard to cesium removal has been observed between 50 and 80 C for CST [1] and at 65 C for RF resin [2]. In addition, the waste supernate solution will boil around 130 C. If the columns boiled dry, the sorbent material could plug the column and lead to replacement of the entire column module. Alternatively, for organic resins such as RF there is risk of fire at elevated temperatures. The objective of the work is to compute temperature distributions across CST- and RF-packed columns immersed in waste supernate under accident scenarios involving loss of salt solution flow through the beds and, in some cases, loss of coolant system flow. For some cases, temperature distributions are determined as a function of time after the initiation of a given accident scenario and in other cases only the final steady-state temperature distributions are calculated. In general, calculations are conducted to ensure conservative and bounding results for the maximum temperatures achievable using the current baseline column design. This information will assist in SCIX design and facility maintenance.

  9. Estimation of Sorption Behavior of Europium(III) Using Biotite Flakes - 13272

    SciTech Connect (OSTI)

    Sasaki, Go; Niibori, Yuichi; Mimura, Hitoshi [Dept. of Quantum Science and Energy Engineering, Graduate School of Engineering, Tohoku University, 6-6-01-2 Aobayama, Aoba-ku, Sendai 980-8579 (Japan)] [Dept. of Quantum Science and Energy Engineering, Graduate School of Engineering, Tohoku University, 6-6-01-2 Aobayama, Aoba-ku, Sendai 980-8579 (Japan); Kirishima, Akira [Institute of Multidisciplinary Research for Advanced Materials Tohoku University 2-1-1 Katahira, Aobaku, Sendai 980-8577 (Japan)] [Institute of Multidisciplinary Research for Advanced Materials Tohoku University 2-1-1 Katahira, Aobaku, Sendai 980-8577 (Japan)

    2013-07-01T23:59:59.000Z

    The interaction of biotite and Eu(III) (europium (III)) was examined by using secondary ion-microprobe mass spectrometer (SIMS), fluorescence emission spectrum and decay behavior of fluorescence emission spectrum in addition to the time-changes of Eu(III) and potassium ions concentrations in a solution, using the flake form samples. The results of SIMS showed that the intensity of Eu was gradually decreasing with depth, while the intensity of Eu in the case shaken for 30 days exceeded that in the case for 1 day. Furthermore, the spatial distribution of Eu(III) and potassium ions in the flake of biotite suggested that Eu ions diffuse mainly from the edges of biotite flake, while Eu ions can slightly diffuse through some small cracks existing on the flake surface far from the edges. Besides, the elution amount of potassium from the biotite flakes into a solution was proportional to the sorption amount of Eu(III). The changes nearly revealed ion exchange between these ions, while muscovite flake sample did not show such ion exchange reaction. In addition, from the time-change of Eu(III) concentration, an apparent diffusion coefficient was estimated to be 8.0x10{sup -12} m{sup 2}/s, by using two-dimensional diffusion model coupled with a film between the solid phase and the liquid phase. Furthermore, the fluorescent intensity decreased with the shaking (contacting) time. This means that Eu(III) gradually diffuses into the inside of biotite edges of the biotite flakes, after the sorption of Eu(III) in the edges. This tendency was observed also in the powder samples. The observed fluorescence decay (at 592 nm in wave length) showed almost similar curve in any samples, indicating a certain sorption form of Eu(III) onto the edges of the biotite flakes. These results mentioned above suggest that the diffusion processes through internal layer in biotite mainly control the sorption behavior of multivalent ions. Such diffusion processes affect the retardation-effects on fracture surfaces in the rock matrix, depending on the fluid flow velocity of groundwater. That is, a more reliable model considering the mass transfer in the internal layer of biotite may be required to estimate the sorption behavior of RNs with biotite which controls the whole sorption behavior of granite. (authors)

  10. RAPID DETERMINATION OF ACTINIDES IN URINE BY INDUCTIVELY-COUPLED PLASMA MASS SPECTROMETRY AND ALPHA SPECTROMETRY: A HYBRID APPROACH

    SciTech Connect (OSTI)

    Maxwell, S.; Jones, V.

    2009-05-27T23:59:59.000Z

    A new rapid separation method that allows separation and preconcentration of actinides in urine samples was developed for the measurement of longer lived actinides by inductively coupled plasma mass spectrometry (ICP-MS) and short-lived actinides by alpha spectrometry; a hybrid approach. This method uses stacked extraction chromatography cartridges and vacuum box technology to facilitate rapid separations. Preconcentration, if required, is performed using a streamlined calcium phosphate precipitation. Similar technology has been applied to separate actinides prior to measurement by alpha spectrometry, but this new method has been developed with elution reagents now compatible with ICP-MS as well. Purified solutions are split between ICP-MS and alpha spectrometry so that long- and short-lived actinide isotopes can be measured successfully. The method allows for simultaneous extraction of 24 samples (including QC samples) in less than 3 h. Simultaneous sample preparation can offer significant time savings over sequential sample preparation. For example, sequential sample preparation of 24 samples taking just 15 min each requires 6 h to complete. The simplicity and speed of this new method makes it attractive for radiological emergency response. If preconcentration is applied, the method is applicable to larger sample aliquots for occupational exposures as well. The chemical recoveries are typically greater than 90%, in contrast to other reported methods using flow injection separation techniques for urine samples where plutonium yields were 70-80%. This method allows measurement of both long-lived and short-lived actinide isotopes. 239Pu, 242Pu, 237Np, 243Am, 234U, 235U and 238U were measured by ICP-MS, while 236Pu, 238Pu, 239Pu, 241Am, 243Am and 244Cm were measured by alpha spectrometry. The method can also be adapted so that the separation of uranium isotopes for assay is not required, if uranium assay by direct dilution of the urine sample is preferred instead. Multiple vacuum box locations may be set-up to supply several ICP-MS units with purified sample fractions such that a high sample throughput may be achieved, while still allowing for rapid measurement of short-lived actinides by alpha spectrometry.

  11. 230Th-234U Age-Dating Uranium by Mass Spectrometry

    SciTech Connect (OSTI)

    Williams, R W; Gaffney, A M

    2012-04-18T23:59:59.000Z

    This is the standard operating procedure used by the Isotope Ratio Mass Spectrometry Group of the Chemical Sciences Division at LLNL for the preparation of a sample of uranium oxide or uranium metal for {sup 230}Th-{sup 234}U age-dating. The method described here includes the dissolution of a sample of uranium oxide or uranium metal, preparation of a secondary dilution, spiking of separate aliquots for uranium and thorium isotope dilution measurements, and purification of uranium and thorium aliquots for mass spectrometry. This SOP may be applied to uranium samples of unknown purity as in a nuclear forensic investigation, and also to well-characterized samples such as, for example, U{sub 3}O{sub 8} and U-metal certified reference materials. The sample of uranium is transferred to a quartz or PFA vial, concentrated nitric acid is added and the sample is heated on a hotplate at approximately 100 C for several hours until it dissolves. The sample solution is diluted with water to make the solution approximately 4 M HNO{sub 3} and hydrofluoric acid is added to make it 0.05 M HF. A secondary dilution of the primary uranium solution is prepared. Separate aliquots for uranium and thorium isotope dilution measurements are taken and spiked with {sup 233}U and {sup 229}Th, respectively. The spiked aliquot for uranium isotope dilution analysis is purified using EiChrom UTEVA resin. The spiked aliquot for thorium isotope dilution analysis is purified by, first, a 1.8 mL AG1x8 resin bed in 9 M HCl on which U adsorbs and Th passes through; second, adsorbing Th on a 1 mL AG1x8 resin bed in 8 M HNO{sub 3} and then eluting it with 9 M HCl followed by 0.1 M HCl + 0.005 M HF; and third, by passing the Th through a final 1.0 mL AG1x8 resin bed in 9 M HCl. The mass spectrometry is performed using the procedure 'Th and U Mass Spectrometry for {sup 230}Th-{sup 234}U Age Dating'.

  12. Small Column Ion Exchange Testing of Superlig 644 for Removal of 137Cs from Hanford Tank Waste Envelope C (Tank 241-AN-107)

    SciTech Connect (OSTI)

    DE Kurath; DL Blanchard; JR Bontha

    2000-06-28T23:59:59.000Z

    The current BNFL Inc. flowsheet for the pretreatment of the Hanford high-level tank wastes includes the use of Superlig{reg_sign} materials for removing {sup 137}Cs from the aqueous fraction of the waste. The Superlig materials applicable to cesium removal include the cesium-selective Superlig 632and Superlig 644. These materials have been developed and supplied by IBC Advanced Technologies, Inc., American Fork, Utah. This report describes the testing of the Superlig 644 ion exchange material in a small dual-column system. The bed volume of the lead column was 18.6 mL (L/D = 7), and the bed volume of the lag column was 15.9 mL (L/D = 6) during the loading phase. The sample processed was approximately 1.6 L of diluted waste ([Na{sup +}] = 4.84 M) from Tank 241-AN-107 (Envelope C). This sample had been previously treated for removal of Sr/transuranic (TRU) values and clarified in a single tube cross-flow filtration unit. All ion exchange process steps were tested, including resin-bed preparation, loading, feed displacement, water rinse, elution, eluant rinse, and resin regeneration. A summary of performance measures for both columns is shown in Table S1. The Cs {lambda} values represent a measure of the effective capacity of the SL-644 resin. The Cs {lambda} of 20 for the lead column is much lower than the estimated 150 obtained by the Savannah River Technology Center during Phase 1A testing. Equilibrium data obtained with batch contacts using the AN-107 Cs IX feed predicts a Cs {lambda} of 183. A Cs {lambda} for the lag column could not be determined due to insufficient breakthrough, but it appeared to work well and removed nearly all of the cesium not removed by the lead column. The low value for the lead column indicates that it did not perform as expected. This may have been due to air or gas in the bed that caused fluid channeling or blinding of the resin. The maximum decontamination factor (DF) for {sup 137}Cs listed in Table S1 is based on {sup 137}Cs concentration in the first samples collected from each column and the {sup 137}Cs concentration in the feed. The composite DF for {sup 137}Cs was 1,760, which provided an effluent with a {sup 137}Cs concentration of 8.7E-02 Ci/m{sup 3}. The {sup 137}Cs concentration is below the basis of design limit and is 7.2% of the contract limit for {sup 137}Cs.

  13. Evaluation of kinetic phosphorescence analysis for the determination of uranium

    SciTech Connect (OSTI)

    Croatto, P.V.; Frank, I.W.; Johnson, K.D.; Mason, P.B.; Smith, M.M.

    1997-12-01T23:59:59.000Z

    In the past, New Brunswick Laboratory (NBL) has used a fluorometric method for the determination of sub-microgram quantities of uranium. In its continuing effort to upgrade and improve measurement technology, NBL has evaluated the commercially-available KPA-11 kinetic phosphorescence analyzer (Chemchek, Richland, WA). The Chemchek KPA-11 is a bench-top instrument which performs single-measurement, quench-corrected analyses for trace uranium. It incorporates patented kinetic phosphorimetry techniques to measure and analyze sample phosphorescence as a function of time. With laser excitation and time-corrected photon counting, the KPA-11 has a lower detection limit than conventional fluorometric methods. Operated with a personal computer, the state-of-the-art KPA-11 offers extensive time resolution and phosphorescence lifetime capabilities for additional specificity. Interferences are thereby avoided while obtaining precise measurements. Routine analyses can be easily and effectively accomplished, with the accuracy and precision equivalent to the pulsed-laser fluorometric method presently performed at NBL, without the need for internal standards. Applications of kinetic phosphorimetry at NBL include the measurement of trace level uranium in retention tank, waste samples, and low-level samples. It has also been used to support other experimental activities at NBL by the measuring of nanogram amounts of uranium contamination (in blanks) in isotopic sample preparations, and the determining of elution curves of different ion exchange resins used for uranium purification. In many cases, no pretreatment of samples was necessary except to fume them with nitric acid, and then to redissolve and dilute them to an appropriate concentration with 1 M HNO{sub 3} before measurement. Concentrations were determined on a mass basis ({micro}g U/g of solution), but no density corrections were needed since all the samples (including the samples used for calibration) were in the same density matrix (1 M HNO{sub 3}). A statistical evaluation of the determination of uranium using kinetic phosphorimetry is described in this report, along with a discussion of the method, and an evaluation of the use of plastic versus quartz cuvettes. Measurement with a precision of {+-} 3--4% relative standard deviation (RSD) and an accuracy of better than {+-} 2% relative difference (RD) are obtained in the 0.0006 to 5 {micro}g U/g-solution range. The instrument detection limit is 0.04 ppb (4 x 10{sup {minus}5} {micro}g U/g solution) using quartz cells, and 0.11 ppb (11 x 10{sup {minus}5} {micro}g U/g solution) using disposable methacrylate cuvettes.

  14. Recovery of minor actinides from spent fuel using TPEN-immobilized gels

    SciTech Connect (OSTI)

    Koyama, S.; Suto, M.; Ohbayashi, H. [Oarai Research and Development Center, Japan Atomic Energy Agency, Oarai (Japan); Oaki, H. [Solutions Research Organization, Tokyo Institute of Technology, Tokyo (Japan); Takeshita, K. [Research Laboratory for Nuclear Reactors, Tokyo Institute of Technology, Tokyo (Japan)

    2013-07-01T23:59:59.000Z

    A series of separation experiments was performed in order to study the recovery process for minor actinides (MAs), such as americium (Am) and curium (Cm), from the actual spent fuel by using an extraction chromatographic technique. N,N,N',N'-tetrakis-(4-propenyloxy-2-pyridylmethyl) ethylenediamine (TPPEN) is an N,N,N',N'-tetrakis (2-pyridylmethyl) ethylenediamine (TPEN) analogue consisting of an incorporated pyridine ring that acts as not only a ligand but also as a site for polymerization and crosslinking of the gel. The TPPEN and N-isopropylacrylamide (NIPA) were dissolved into dimethylformamide (DMF, Wako Co., Ltd.) and a silica beads polymer, and then TTPEN was immobilized chemically in a polymer gel (so called TPEN-gel). Mixed oxide (MOX) fuel, which was highly irradiated up to 119 GWD/MTM in the experimental fast reactor Joyo, was used as a reference spent fuel. First, uranium (U) and plutonium (Pu) were separated from the irradiated fuel using an ion-exchange method, and then, the platinum group elements were removed by CMPO to leave a mixed solution of MAs and lanthanides. The 3 mol% TPPEN-gel was packed with as an extraction column (CV: 1 ml) and then rinsed by 0.1 M NaNO{sub 3}(pH 4.0) for pH adjustment. After washing the column by 0.01 M NaNO{sub 3} (pH 4.0), Eu was detected and the recovery rate reached 93%. The MAs were then recovered by changing the eluent to 0.01 M NaNO{sub 3} (pH 2.0), and the recovery rate of Am was 48 %. The 10 mol% TPPEN-gel was used to improve adsorption coefficient of Am and a condition of eluent temperature was changed in order to confirm the temperature swing effect on TPEN-gel for MA. More than 90% Eu was detected in the eluent after washing with 0.01 M NaNO{sub 3} (pH 3.5) at 5 Celsius degrees. Americium was backwardly detected and eluted continuously during the same condition. After removal of Eu, the eluent temperature was changed to 32 Celsius degrees, then Am was detected (pH 3.0). Finally remained Am could be stripped from TPPEN-gel by changing the pH of the eluent to 2.0. These results These results prove that the proposed recovery process for MAs is a potential candidate for future reprocessing methods based on the extraction chromatographic technique. (authors)

  15. Ion Exchange Studies for Removal of Sulfate from Hanford Tank Waste Envelope C (241-AN-107) Using SuperLig 655 Resin

    SciTech Connect (OSTI)

    DE Kurath; JR Bontha; DL Blanchard; SK Fiskum; BM Rapko

    2000-08-23T23:59:59.000Z

    BNFL Inc. is evaluating various pretreatment technologies to mitigate the impacts of sulfate on the LAW vitrification system. One pretreatment technology for separating sulfate from LAW solutions involves the use of SuperLig{reg_sign} 655 (SL-655), a proprietary ion exchange material developed and supplied by IBC Advanced Technologies, Inc., American Fork, UT. This report describes testing of SL-655 with diluted ([Na] {approximately} 5 M) waste from Hanford Tank 241-AN-107 at Battelle, Pacific Northwest Division. Batch contact studies were conducted from 4 to 96 hours to determine the sulfate distribution coefficient and reaction kinetics. A small-scale ion exchange column test was conducted to evaluate sulfate removal, loading, breakthrough, and elution from the SL-655. In all of these tests, an archived 241-AN-107 tank waste sample (pretreated to remove Cs, Sr, and transuranics elements) was used. The experimental details and results are described in this report. Under the test conditions, SL-655 was found to have no significant ion exchange affinity for sulfate in this matrix. The batch contact study resulted in no measurable difference in the aqueous sulfate concentration following resin contact (K{sub d} {approximately} 0). The column test also demonstrated SL-655 had no practical affinity for sulfate in the tested matrix. Within experimental error, the sulfate concentration in the column effluent was equal to the concentration in the feed after passing 3 bed volumes of sample through the columns. Furthermore, some, if not all, of the decreased sulfate concentration in these first three column volumes of effluent can be ascribed to mixing and dilution of the 241-AN-107 feed with the interstitial liquid present in the column at the start of the loading cycle. Finally, ICP-AES measurements on the eluate solutions showed the presence of barium as soon as contact with the feed solution is completed. Barium is a metal not detected in the feed solution. Should the loss of barium be correlated with the resin's ability to selectively complex sulfate, then maintaining even the current limited resin characteristics for sulfate complexation over multiple cycles becomes questionable.

  16. Development Of Ion Chromatography Methods To Support Testing Of The Glycolic Acid Reductant Flowsheet In The Defense Waste Processing Facility

    SciTech Connect (OSTI)

    Wiedenman, B. J.; White, T. L.; Mahannah, R. N.; Best, D. R.; Stone, M. E.; Click, D. R.; Lambert, D. P.; Coleman, C. J.

    2013-10-01T23:59:59.000Z

    Ion Chromatography (IC) is the principal analytical method used to support studies of Sludge Reciept and Adjustment Tank (SRAT) chemistry at DWPF. A series of prior analytical ''Round Robin'' (RR) studies included both supernate and sludge samples from SRAT simulant, previously reported as memos, are tabulated in this report.2,3 From these studies it was determined to standardize IC column size to 4 mm diameter, eliminating the capillary column from use. As a follow on test, the DWPF laboratory, the PSAL laboratory, and the AD laboratory participated in the current analytical RR to determine a suite of anions in SRAT simulant by IC, results also are tabulated in this report. The particular goal was to confirm the laboratories ability to measure and quantitate glycolate ion. The target was + or - 20% inter-lab agreement of the analyte averages for the RR. Each of the three laboratories analyzed a batch of 12 samples. For each laboratory, the percent relative standard deviation (%RSD) of the averages on nitrate, glycolate, and oxalate, was 10% or less. The three laboratories all met the goal of 20% relative agreement for nitrate and glycolate. For oxalate, the PSAL laboratory reported an average value that was 20% higher than the average values reported by the DWPF laboratory and the AD laboratory. Because of this wider window of agreement, it was concluded to continue the practice of an additional acid digestion for total oxalate measurement. It should also be noted that large amounts of glycolate in the SRAT samples will have an impact on detection limits of near eluting peaks, namely Fluoride and Formate. A suite of scoping experiments are presented in the report to identify and isolate other potential interlaboratory disceprancies. Specific ion chromatography inter-laboratory method conditions and differences are tabulated. Most differences were minor but there are some temperature control equipment differences that are significant leading to a recommendation of a heated jacket for analytical columns that are remoted for use in radiohoods. A suggested method improvement would be to implement column temperture control at a temperature slightly above ambient to avoid peak shifting due to temperature fluctuations. Temperature control in this manner would improve short and longer term peak retention time stability. An unknown peak was observed during the analysis of glycolic acid and SRAT simulant. The unknown peak was determined to best match diglycolic acid. The development of a method for acetate is summaraized, and no significant amount of acetate was observed in the SRAT products tested. In addition, an alternative Gas Chromatograph (GC) method for glycolate is summarized.

  17. LOW ACTIVITY WASTE FEED SOLIDS CARACTERIZATION AND FILTERABILITY TESTS

    SciTech Connect (OSTI)

    McCabe, D.; Crawford, C.; Duignan, M.; Williams, M.; Burket, P.

    2014-04-03T23:59:59.000Z

    The primary treatment of the tank waste at the DOE Hanford site will be done in the Waste Treatment and Immobilization Plant (WTP) that is currently under construction. The baseline plan for the WTP Pretreatment facility is to treat the waste, splitting it into High Level Waste (HLW) feed and Low Activity Waste (LAW) feed. Both waste streams are then separately vitrified as glass and sealed in canisters. The LAW glass will be disposed onsite in the Integrated Disposal Facility (IDF). There are currently no plans to treat the waste to remove technetium in the WTP Pretreatment facility, so its disposition path is the LAW glass. Options are being explored to immobilize the LAW portion of the tank waste, i.e., the LAW feed from the WTP Pretreatment facility. Removal of {sup 99}Tc from the LAW Feed, followed by off-site disposal of the {sup 99}Tc, would eliminate a key risk contributor for the IDF Performance Assessment (PA) for supplemental waste forms, and has potential to reduce treatment and disposal costs. Washington River Protection Solutions (WRPS) is developing some conceptual flow sheets for LAW treatment and disposal that could benefit from technetium removal. One of these flowsheets will specifically examine removing {sup 99}Tc from the LAW feed stream to supplemental immobilization. The conceptual flow sheet of the {sup 99}Tc removal process includes a filter to remove insoluble solids prior to processing the stream in an ion exchange column, but the characteristics and behavior of the liquid and solid phases has not previously been investigated. This report contains results of testing of a simulant that represents the projected composition of the feed to the Supplemental LAW process. This feed composition is not identical to the aqueous tank waste fed to the Waste Treatment Plant because it has been processed through WTP Pretreatment facility and therefore contains internal changes and recycle streams that will be generated within the WTP process. Although a Supplemental LAW feed simulant has previously been prepared, this feed composition differs from that simulant because those tests examined only the fully soluble aqueous solution at room temperature, not the composition formed after evaporation, including the insoluble solids that precipitate after it cools. The conceptual flow sheet for Supplemental LAW immobilization has an option for removal of {sup 99}Tc from the feed stream, if needed. Elutable ion exchange has been selected for that process. If implemented, the stream would need filtration to remove the insoluble solids prior to processing in an ion exchange column. The characteristics, chemical speciation, physical properties, and filterability of the solids are important to judge the feasibility of the concept, and to estimate the size and cost of a facility. The insoluble solids formed during these tests were primarily natrophosphate, natroxalate, and a sodium aluminosilicate compound. At the elevated temperature and 8 M [Na+], appreciable insoluble solids (1.39 wt%) were present. Cooling to room temperature and dilution of the slurry from 8 M to 5 M [Na+] resulted in a slurry containing 0.8 wt% insoluble solids. The solids (natrophosphate, natroxalate, sodium aluminum silicate, and a hydrated sodium phosphate) were relatively stable and settled quickly. Filtration rates were in the range of those observed with iron-based simulated Hanford tank sludge simulants, e.g., 6 M [Na+] Hanford tank 241-AN-102, even though their chemical speciation is considerably different. Chemical cleaning of the crossflow filter was readily accomplished with acid. As this simulant formulation was based on an average composition of a wide range of feeds using an integrated computer model, this exact composition may never be observed. But the test conditions were selected to enable comparison to the model to enable improving its chemical prediction capability.

  18. Multiscale analysis of nonlinear systems using computational homology

    SciTech Connect (OSTI)

    Konstantin Mischaikow, Rutgers University /Georgia Institute of Technology, Michael Schatz, Georgia Institute of Technology, William Kalies, Florida Atlantic University, Thomas Wanner,George Mason University

    2010-05-19T23:59:59.000Z

    This is a collaborative project between the principal investigators. However, as is to be expected, different PIs have greater focus on different aspects of the project. This report lists these major directions of research which were pursued during the funding period: (1) Computational Homology in Fluids - For the computational homology effort in thermal convection, the focus of the work during the first two years of the funding period included: (1) A clear demonstration that homology can sensitively detect the presence or absence of an important flow symmetry, (2) An investigation of homology as a probe for flow dynamics, and (3) The construction of a new convection apparatus for probing the effects of large-aspect-ratio. (2) Computational Homology in Cardiac Dynamics - We have initiated an effort to test the use of homology in characterizing data from both laboratory experiments and numerical simulations of arrhythmia in the heart. Recently, the use of high speed, high sensitivity digital imaging in conjunction with voltage sensitive fluorescent dyes has enabled researchers to visualize electrical activity on the surface of cardiac tissue, both in vitro and in vivo. (3) Magnetohydrodynamics - A new research direction is to use computational homology to analyze results of large scale simulations of 2D turbulence in the presence of magnetic fields. Such simulations are relevant to the dynamics of black hole accretion disks. The complex flow patterns from simulations exhibit strong qualitative changes as a function of magnetic field strength. Efforts to characterize the pattern changes using Fourier methods and wavelet analysis have been unsuccessful. (4) Granular Flow - two experts in the area of granular media are studying 2D model experiments of earthquake dynamics where the stress fields can be measured; these stress fields from complex patterns of 'force chains' that may be amenable to analysis using computational homology. (5) Microstructure Characterization - We extended our previous work on studying the time evolution of patterns associated with phase separation in conserved concentration fields. (6) Probabilistic Homology Validation - work on microstructure characterization is based on numerically studying the homology of certain sublevel sets of a function, whose evolution is described by deterministic or stochastic evolution equations. (7) Computational Homology and Dynamics - Topological methods can be used to rigorously describe the dynamics of nonlinear systems. We are approaching this problem from several perspectives and through a variety of systems. (8) Stress Networks in Polycrystals - we have characterized stress networks in polycrystals. This part of the project is aimed at developing homological metrics which can aid in distinguishing not only microstructures, but also derived mechanical response fields. (9) Microstructure-Controlled Drug Release - This part of the project is concerned with the development of topological metrics in the context of controlled drug delivery systems, such as drug-eluting stents. We are particularly interested in developing metrics which can be used to link the processing stage to the resulting microstructure, and ultimately to the achieved system response in terms of drug release profiles. (10) Microstructure of Fuel Cells - we have been using our computational homology software to analyze the topological structure of the void, metal and ceramic components of a Solid Oxide Fuel Cell.

  19. Revised Thermal Analysis of LANL Ion Exchange Column

    SciTech Connect (OSTI)

    Laurinat, J

    2006-04-11T23:59:59.000Z

    This document updates a previous calculation of the temperature distributions in a Los Alamos National Laboratory (LANL) ion exchange column.1 LANL operates two laboratory-scale anion exchange columns, in series, to extract Pu-238 from nitric acid solutions. The Defense Nuclear Facilities Safety Board has requested an updated analysis to calculate maximum temperatures for higher resin loading capacities obtained with a new formulation of the Reillex HPQ anion exchange resin. The increased resin loading capacity will not exceed 118 g plutonium per L of resin bed. Calculations were requested for normal operation of the resin bed at the minimum allowable solution feed rate of 30 mL/min and after an interruption of flow at the end of the feed stage, when one of the columns is fully loaded. The object of the analysis is to demonstrate that the decay heat from the Pu-238 will not cause resin bed temperatures to increase to a level where the resin significantly degrades. At low temperatures, resin bed temperatures increase primarily due to decay heat. At {approx}70 C a Low Temperature Exotherm (LTE) resulting from the reaction between 8-12 M HNO{sub 3} and the resin has been observed. The LTE has been attributed to an irreversible oxidation of pendant ethyl benzene groups at the termini of the resin polymer chains by nitric acid. The ethyl benzene groups are converted to benzoic acid moities. The resin can be treated to permanently remove the LTE by heating a resin suspension in 8M HNO{sub 3} for 30-45 minutes. No degradation of the resin performance is observed after the LTE removal treatment. In fact, heating the resin in boiling ({approx}115-120 C) 12 M HNO{sub 3} for 3 hr displays thermal stability analogous to resin that has been treated to remove the LTE. The analysis is based on a previous study of the SRS Frames Waste Recovery (FWR) column, performed in support of the Pu-238 production campaign for NASA's Cassini mission. In that study, temperature transients following an interruption of flow to the column were calculated. The transient calculations were terminated after the maximum resin bed temperature reached the Technical Standard of 60 C, which was set to prevent significant resin degradation. The LANL column differs from the FWR column in that it has a significantly smaller radius, 3.73 cm nominal versus approximately 28 cm. It follows that natural convection removes heat much more effectively from the LANL column, so that the column may reach thermal equilibrium. Consequently, the calculations for a flow interruption were extended until an approach to thermal equilibrium was observed. The LANL ion exchange process also uses a different resin than was used in the FWR column. The LANL column uses Reillex HPQ{trademark} resin, which is more resistant to attack by nitric acid than the Ionac 641{trademark} resin used in the FWR column. Heat generation from the resin oxidation reaction with nitric acid is neglected in this analysis since LANL will be treating the resin to remove the LTE prior to loading the resin in the columns. Calculations were performed using a finite difference computer code, which incorporates models for absorption and elution of plutonium and for forced and natural convection within the resin bed. Calculations for normal column operation during loading were performed using an initial temperature and a feed temperature equal to the ambient air temperature. The model for the normal flow calculations did not include natural convection within the resin bed. The no flow calculations were started with the temperature and concentration profiles at the end of the loading stage, when there would be a maximum amount of plutonium either adsorbed on the resin or in the feed solution in the column.

  20. Synthesis, spectroscopy, and structural characterization of six-coordinate bis(aryldiazenido)rhenium and bis(diarylhydrazido)rhenium complexes. X-ray structures of (Et{sub 4}N)[Re(NNPh){sub 2}(O{sub 2}C{sub 6}H{sub 4}){sub 2}], (Et{sub 4}N)[Re(NNPh{sub 2}){sub 2}(O{sub 2}C{sub 6}H{sub 4}){sub 2}], and Na[Re(NNPh){sub 2}(O{sub 2}C{sub 6}H{sub 4}){sub 2}]{center_dot}CH{sub 3}CN

    SciTech Connect (OSTI)

    Kettler, P.B.; Chang, Yuan-Da; Zubieta, J. [Syracuse Univ., NY (United States)

    1994-12-07T23:59:59.000Z

    The reactions of the cis-dioxorhenium(VII)-catecholate complex [(CH{sub 3}CH{sub 2}){sub 4}N][ReO{sub 2}(O{sub 2}C{sub 6}H{sub 4}){sub 2}] (1) with either monosubstituted organohydrazines (C{sub 6}H{sub 5}NHNH{sub 2}; 4-BrC{sub 6}H{sub 4}NHNH{sub 2}) or 1,1 disubstituted organohydrazines (Ph{sub 2-}NNH{sub 2}) yield the cis-bis(diazenido) core complexes [(CH{sub 3}CH{sub 2}){sub 4}N][Re(NNR){sub 2}(O{sub 2}C{sub 6}H{sub 4}){sub 2}] (5, R = C{sub 6}H{sub 5}; 6, R = 4-BrC{sub 6}H{sub 4}) and the cis-bis(hydrazido) core species [(CH{sub 3}CH{sub 2}){sub 4}N][Re(NNPh{sub 2}){sub 2}(O{sub 2}C36H{sub 4}){sub 2}(O{sub 2}C36H{sub 4}){sub 2}] (7). Elution of 5 in a 3:1 mixture of toluene/methanol on a column of silica gel resulted in cation exchange to give Na[Re(NNPh){sub 2}-(O{sub 2}C{sub 6}H{sub 4}){sub 2}]{center_dot}CH{sub 3}CN (8) as a one-dimensional polymer ([Na(CH{sub 3}CN)]{sup +}[Re(NNPh){sub 2}(O{sub 2}C{sub 6}H{sub 4}){sub 2}]{sup {minus}}){sub 2}. Crystal data for C{sub 32}H{sub 38}N{sub 5}O{sub 4}Re (5): P2{sub 1}/c,a = 14.458(3) {angstrom}, b = 10.436(2) {angstrom}, c = 21.767(4) {angstrom}, {beta} = 107.04(3){degrees}, V = 3140(2) {angstrom}{sup 3}, Z = 4, D {sub calc} = 1.572 g cm{sup {minus}3}; structure solution and refinement based on 3256 reflections with I{sub o} {ge} 3{sigma}(I{sub o}) converged at R = 0.053. Crystal data for C{sub 44}H{sub 48}N{sub 5}O{sub 4}Re (7): P1, a = 11.660(2) {angstrom}, b = 11.864(2) {angstrom}, c = 15.400(2) {angstrom}, {alpha} = 107.12(3){degrees}, {beta} = 94.99(3){degrees}, {gamma} = 97.61(3){degrees}, V = 2000(1) {angstrom}{sup 3}, Z = 2, D{sub calc} = 1.490 g cm{sup {minus}3}; 3702 reflections, R = 0.0534. Crystal data for C{sub 26}H{sub 18}N{sub 5}NaO{sub 4}Re (8): P2/n, a = 5.785(1) {angstrom}, b = 9.670(2) {angstrom}, c = 23.142(5) {angstrom}. {beta} = 90.91(30)degrees, V = 1294.4(7) {angstrom}{sup 3}, Z = 2, D{sub calc} = 1.737 g cm{sup {minus}3}; 1517 reflections, R = 0.049.

  1. Multiscale analysis of nonlinear systems using computational homology

    SciTech Connect (OSTI)

    Konstantin Mischaikow; Michael Schatz; William Kalies; Thomas Wanner

    2010-05-24T23:59:59.000Z

    This is a collaborative project between the principal investigators. However, as is to be expected, different PIs have greater focus on different aspects of the project. This report lists these major directions of research which were pursued during the funding period: (1) Computational Homology in Fluids - For the computational homology effort in thermal convection, the focus of the work during the first two years of the funding period included: (1) A clear demonstration that homology can sensitively detect the presence or absence of an important flow symmetry, (2) An investigation of homology as a probe for flow dynamics, and (3) The construction of a new convection apparatus for probing the effects of large-aspect-ratio. (2) Computational Homology in Cardiac Dynamics - We have initiated an effort to test the use of homology in characterizing data from both laboratory experiments and numerical simulations of arrhythmia in the heart. Recently, the use of high speed, high sensitivity digital imaging in conjunction with voltage sensitive fluorescent dyes has enabled researchers to visualize electrical activity on the surface of cardiac tissue, both in vitro and in vivo. (3) Magnetohydrodynamics - A new research direction is to use computational homology to analyze results of large scale simulations of 2D turbulence in the presence of magnetic fields. Such simulations are relevant to the dynamics of black hole accretion disks. The complex flow patterns from simulations exhibit strong qualitative changes as a function of magnetic field strength. Efforts to characterize the pattern changes using Fourier methods and wavelet analysis have been unsuccessful. (4) Granular Flow - two experts in the area of granular media are studying 2D model experiments of earthquake dynamics where the stress fields can be measured; these stress fields from complex patterns of 'force chains' that may be amenable to analysis using computational homology. (5) Microstructure Characterization - We extended our previous work on studying the time evolution of patterns associated with phase separation in conserved concentration fields. (6) Probabilistic Homology Validation - work on microstructure characterization is based on numerically studying the homology of certain sublevel sets of a function, whose evolution is described by deterministic or stochastic evolution equations. (7) Computational Homology and Dynamics - Topological methods can be used to rigorously describe the dynamics of nonlinear systems. We are approaching this problem from several perspectives and through a variety of systems. (8) Stress Networks in Polycrystals - we have characterized stress networks in polycrystals. This part of the project is aimed at developing homological metrics which can aid in distinguishing not only microstructures, but also derived mechanical response fields. (9) Microstructure-Controlled Drug Release - This part of the project is concerned with the development of topological metrics in the context of controlled drug delivery systems, such as drug-eluting stents. We are particularly interested in developing metrics which can be used to link the processing stage to the resulting microstructure, and ultimately to the achieved system response in terms of drug release profiles. (10) Microstructure of Fuel Cells - we have been using our computational homology software to analyze the topological structure of the void, metal and ceramic components of a Solid Oxide Fuel Cell.

  2. New Adsorption Cycles for Carbon Dioxide Capture and Concentration

    SciTech Connect (OSTI)

    James Ritter; Armin Ebner; Steven Reynolds Hai Du; Amal Mehrotra

    2008-07-31T23:59:59.000Z

    The objective of this three-year project was to study new pressure swing adsorption (PSA) cycles for CO{sub 2} capture and concentration at high temperature. The heavy reflux (HR) PSA concept and the use of a hydrotalcite like (HTlc) adsorbent that captures CO{sub 2} reversibly at high temperatures simply by changing the pressure were two key features of these new PSA cycles. Through the completion or initiation of nine tasks, a bench-scale experimental and theoretical program has been carried out to complement and extend the process simulation study that was carried out during Phase I (DE-FG26-03NT41799). This final report covers the entire project from August 1, 2005 to July 31, 2008. This program included the study of PSA cycles for CO{sub 2} capture by both rigorous numerical simulation and equilibrium theory analysis. The insight gained from these studies was invaluable toward the applicability of PSA for CO{sub 2} capture, whether done at ambient or high temperature. The rigorous numerical simulation studies showed that it is indeed possible to capture and concentrate CO{sub 2} by PSA. Over a wide range of conditions it was possible to achieve greater than 90% CO{sub 2} purity and/or greater than 90% CO{sub 2} recovery, depending on the particular heavy reflux (HR) PSA cycle under consideration. Three HR PSA cycles were identified as viable candidates for further study experimentally. The equilibrium theory analysis, which represents the upper thermodynamic limit of the performance of PSA process, further validated the use of certain HR PSA cycles for CO{sub 2} capture and concentration. A new graphical approach for complex PSA cycle scheduling was also developed during the course of this program. This new methodology involves a priori specifying the cycle steps, their sequence, and the number of beds, and then following a systematic procedure that requires filling in a 2-D grid based on a few simple rules, some heuristics and some experience. It has been tested successfully against several cycle schedules taken from the literature, including a 2-bed 4-step Skarstrom cycle, a 4-bed 9-step process with 2 equalization steps, a 9-bed 11-step process with 3 equalization steps, and a 6-bed 13-step process with 4 equalization steps and 4 idle steps. With respect to CO{sub 2} capture and concentration by PSA, this new approach is now providing a very straightforward way to determine all the viable 3-bed, 4-bed, 5-bed, n-bed, etc. HR PSA cycle schedules to explore using both simulation and experimentation. This program also touted the use of K-promoted HTlc as a high temperature, reversible adsorbent for CO{sub 2} capture by PSA. This program not only showed how to use this material in HR PSA cycles, but it also proposed a new CO{sub 2} interaction mechanism in conjunction with a non-equilibrium kinetic model that adequately describes the uptake and release of CO{sub 2} in this material, and some preliminary fixed bed adsorption breakthrough and desorption elution experiments were carried out to demonstrate complete reversibility on a larger scale. This information was essentially missing from the literature and deemed invaluable toward promoting the use of K-promoted HTlc as a high temperature, reversible adsorbent for CO{sub 2} capture by PSA. Overall, the objectives of this project were met. It showed the feasibility of using K-promoted hydrotalcite (HTlc) as a high temperature, reversible adsorbent for CO{sub 2} capture by PSA. It discovered some novel HR PSA cycles that might be useful for this purpose. Finally, it revealed a mechanistic understanding of the interaction of CO{sub 2} with K-promoted HTlc.

  3. The Impact Of The MCU Life Extension Solvent On Sludge Batch 8 Projected Operating Windows

    SciTech Connect (OSTI)

    Peeler, D. K.; Edwards, T. B.; Stone, M. E.

    2013-08-14T23:59:59.000Z

    As a part of the Actinide Removal Process (ARP)/Modular Caustic Side Solvent Extraction Unit (MCU) Life Extension Project, a next generation solvent (NGS) and a new strip acid will be deployed. The strip acid will be changed from dilute nitric acid to dilute boric acid (0.01 M). Because of these changes, experimental testing or evaluations with the next generation solvent are required to determine the impact of these changes (if any) to Chemical Process Cell (CPC) activities, glass formulation strategies, and melter operations at the Defense Waste Processing Facility (DWPF). The introduction of the dilute (0.01M) boric acid stream into the DWPF flowsheet has a potential impact on glass formulation and frit development efforts since B2O3 is a major oxide in frits developed for DWPF. Prior knowledge of this stream can be accounted for during frit development efforts but that was not the case for Sludge Batch 8 (SB8). Frit 803 has already been recommended and procured for SB8 processing; altering the frit to account for the incoming boron from the strip effluent (SE) is not an option for SB8. Therefore, the operational robustness of Frit 803 to the introduction of SE including its compositional tolerances (i.e., up to 0.0125M boric acid) is of interest and was the focus of this study. The primary question to be addressed in the current study was: What is the impact (if any) on the projected operating windows for the Frit 803 SB8 flowsheet to additions of B2O3 from the SE in the Sludge Receipt and Adjustment Tank (SRAT)? More specifically, will Frit 803 be robust to the potential compositional changes occurring in the SRAT due to sludge variation, varying additions of ARP and/or the introduction of SE by providing access to waste loadings (WLs) of interest to DWPF? The Measurement Acceptability Region (MAR) results indicate there is very little, if any, impact on the projected operating windows for the Frit 803 SB8 system regardless of the presence or absence of ARP and SE (up to 2 wt% B2O3 contained in the SRAT and up to 2000 gallons of ARP). It should be noted that 0.95 wt% B2O3 is the nominal projected concentration in the SRAT based on a 0.0125M boric acid flowsheet with 70,000 liters of SE being added to the SRAT. The impact on CPC processing of a 0.01M boric acid solution for elution of cesium during Modular Caustic Side Solvent Extraction Unit (MCU) processing has previously been evaluated by the Savannah River National Laboratory (SRNL). Increasing the acid strength to 0.0125M boric acid to account for variations in the boric acid strength has been reviewed versus the previous evaluation. The amount of acid from the boric acid represented approximately 5% of the total acid during the previous evaluation. An increase from 0.01 to 0.0125M boric acid represents a change of approximately 1.3% which is well within the error of the acid calculation. Therefore, no significant changes to CPC processing (hydrogen generation, metal solubilities, rheological properties, REDOX control, etc.) are expected from an increase in allowable boric acid concentration from 0.01M to 0.0125M.