Powered by Deep Web Technologies
Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


1

An Improved Synthesis of BrettPhos- and RockPhos-Type Biarylphosphine Ligands  

E-Print Network (OSTI)

Improved processes for the preparation of biphenyl-based phosphine ligands t-BuBrettPhos, RockPhos, and BrettPhos are presented. The new methods, featuring the use of Grignard reagents and catalytic amounts of copper, are ...

Hoshiya, Naoyuki

2

Test of an LED Monitoring System for the PHOS Spectrometer  

E-Print Network (OSTI)

Preprint submitted to Elsevier Print on 26th January 2000A prototype monitoring system for the Photon Spectrometer (PHOS) of the ALICE experiment at LHC is described in detail. The prototype consists of Control and Master modules. The first one is 8x8 matrix of Light Emitting Diodes coupled with stable generators of current pulses. The system provides an individual control for each of the 64 channels of PHOS prototype based on lead-tungstate crystals. A long term stability of order of 10-3 has been achieved in integral beam tests of the monitoring system and PHOS prototypes.

Blick, A M; Erin, S V; Kharlov, Yu V; Lobanov, M O; Mikhailov, Yu V; Minaev, N G; Petrov, V A; Sadovsky, S A; Samoylenko, V D; Suzdalev, V I; Senko, V A; Tikhonov, V V

1999-01-01T23:59:59.000Z

3

Method for fluorinating coal  

DOE Patents (OSTI)

Coal is fluorinated by contact with fluorine gas at low pressure. After pial fluorination, when the reaction rate has slowed, the pressure is slowly increased until fluorination is complete, forming a solid fluorinated coal of approximate composition CF.sub.1.55 H.sub.0.15. The fluorinated coal and a solid distillate resulting from vacuum pyrolysis of the fluorinated coal are useful as an internal standard for mass spectrometric unit mass assignments from about 100 to over 1500.

Huston, John L. (Skokie, IL); Scott, Robert G. (Westmont, IL); Studier, Martin H. (Downers Grove, IL)

1978-01-01T23:59:59.000Z

4

Trigger region unit for the ALICE PHOS calorimeter  

E-Print Network (OSTI)

The Photon Spectrometer (PHOS) of ALICE measures electromagnetic showers of up to 100 GeV via a large matrix of PWO crystals, each read out by an APD. Trigger regions consist of 28*16 crystals, inter-connected via analogue signals generated on front-end cards and transmitted to Trigger Region Units (TRU) which digitize and process the analogue hit information. Eight TRU cards are embedded inside each PHOS module in water-cooled cassettes, each inserted between a block 14 FEE readout cards. Analogue sums are generated by fast summing shapers, with their outputs connected to the TRU via equal-length differential cables. The TRU receives analogue sums on 112 inputs and digitizes these via 12 bit ADCs which are inter-connected with a central FPGA via serial LVDS links. The level-0 and level-1 trigger algorithms are based on pipelined charge summing over 4 consecutive samples and over 4*4 crystal windows. Low latency level-0 decisions and more refined level-1 decisions are generated as a 40 MHz Yes/No sequence whi...

Müller, Hans; Li Qing Xia; Pimenta, Rui; Röhrich, Dieter; Skaali, Bernhard; Oltean, Alexandra

2005-01-01T23:59:59.000Z

5

Partially fluorinated ionic compounds  

DOE Patents (OSTI)

Partially fluorinated ionic compounds are prepared. They are useful in the preparation of partially fluorinated dienes, in which the repeat units are cycloaliphatic.

Han, legal representative, Amy Qi (Hockessin, DE); Yang, Zhen-Yu (Hockessin, DE)

2008-11-25T23:59:59.000Z

6

FLUORINATION PROCESS  

DOE Patents (OSTI)

A process for the fluorination of uranium metal is described. It is known that uranium will react with liquid chlorine trifluoride but the reaction proceeds at a slow rate. However, a mixture of a halogen trifluoride together with hydrogen fluoride reacts with uranium at a significantly faster rate than does a halogen trifluoride alone. Bromine trifluoride is suitable for use in the process, but chlorine trifluoride is preferred. Particularly suitable is a mixture of ClF/sub 3/ and HF having a mole ratio (moles

McMillan, T.S.

1957-10-29T23:59:59.000Z

7

Environmental Protection Agency 61.220 (iii) The quantity (in pounds) of phos-  

E-Print Network (OSTI)

for the phosphogypsum; (vi) A copy of each certification doc- ument which accompanied the phos- phogypsum at the time or transfer of phosphogypsum to a person other than an agricultural end- user, the distributor, retailer information: (1) The name and address of the per- son in charge of the activity involving use of phosphogypsum

8

Fluorination process using catalysts  

DOE Patents (OSTI)

A process is given for converting an actinide compound selected from the group consisting of uranium oxides, plutonium oxides, uranium tetrafluorides, plutonium tetrafluorides and mixtures of said oxides and tetrafluorides, to the corresponding volatile actinide hexafluoride by fluorination with a stoichiometric excess of fluorine gas. The improvement involves conducting the fluorination of the plutonium compounds in the presence of a fluoride catalyst selected from the group consisting of CoF/sub 3/, AgF/sub 2/ and NiF/sub 2/, whereby the fluorination is significantly enhanced. The improvement also involves conducting the fluorination of one of the uranium compounds in the presence of a fluoride catalyst selected from the group consisting of CoF/sub 3/ and AgF/sub 2/, whereby the fluorination is significantly enhanced.

Hochel, R.C.; Saturday, K.A.

1983-08-25T23:59:59.000Z

9

Fluorination process using catalyst  

DOE Patents (OSTI)

A process for converting an actinide compound selected from the group consisting of uranium oxides, plutonium oxides, uranium tetrafluorides, plutonium tetrafluorides and mixtures of said oxides and tetrafluorides, to the corresponding volatile actinide hexafluoride by fluorination with a stoichiometric excess of fluorine gas. The improvement involves conducting the fluorination of the plutonium compounds in the presence of a fluoride catalyst selected from the group consisting of CoF.sub.3, AgF.sub.2 and NiF.sub.2, whereby the fluorination is significantly enhanced. The improvement also involves conducting the fluorination of one of the uranium compounds in the presence of a fluoride catalyst selected from the group consisting of CoF.sub.3 and AgF.sub.2, whereby the fluorination is significantly enhanced.

Hochel, Robert C. (Aiken, SC); Saturday, Kathy A. (Aiken, SC)

1985-01-01T23:59:59.000Z

10

Fluorine separation and generation device  

DOE Patents (OSTI)

A process and apparatus for the electrolytic separation of fluorine from a mixture of gases is disclosed. Also described is the process and apparatus for the generation of fluorine from fluorine/fluoride containing solids, liquids or gases.

The Regents of the University of California (Oakland, CA)

2008-12-23T23:59:59.000Z

11

Heavily fluorinated electronic polymers  

E-Print Network (OSTI)

Building blocks, containing majority fluorine content by weight, for PPEs and PPVs have been synthesized. Some of the monomers were shown to give exclusively fluorous-phase soluble polymers, the syntheses of which were ...

Lim, Jeewoo

2011-01-01T23:59:59.000Z

12

Fluorinated Precursors of Superconducting Ceramics ...  

Fluorinated precursors for superconducting ceramics typically increase the critical current in the ... Applications and Industries. High-temperature ...

13

DRY FLUORINE SEPARATION METHOD  

DOE Patents (OSTI)

Preparation and separation of U/sup 233/ by irradiation of ThF/sub 4/ is described. During the neutron irradiation to produce Pa/sup 233/ a fluorinating agent such as HF, F/sub 2/, or HF + F/sub 2/ is passed through the ThF/sub 4/ powder to produce PaF/sub 5/. The PaF/sub 5/, being more volatile, is removed as a gas and allowed to decay radioactively to U/sup 233/ fluoride. A batch procedure in which ThO/sub 2/ or Th metal is irradiated and fluorinated is suggested. Some Pa and U fluoride volatilizes away. Then the remainder is fluorinated with F/sub 2/ to produce very volatile UF/sub 6/ which is recovered. (T.R.H.)

Seaborg, G.T.; Gofman, J.W.; Stoughton, R.W.

1959-05-19T23:59:59.000Z

14

Available Technologies: Fluorine Separation and Generation Device  

... and Constantin Stefan of Berkeley Lab have developed a solid state electrolytic cell to separate fluorine from fluorine/fluoride gases or liquids, ...

15

Process for preparing fluorine-18  

DOE Patents (OSTI)

An improved process for preparation of fluorine-18 by a neon (deuteron, alpha particle) fluorine-18 nuclear reaction in a non-reactive enclosed reaction zone wherein a ultrapure product is recovered by heating the reaction zone to a high temperature and removing the product with an inert gas.

Winchell, Harry S. (Lafayette, CA); Wells, Dale K. (Martinez, CA); Lamb, James F. (Albany, CA); Beaudry, Samuel B. (Walnut Creek, CA)

1976-09-21T23:59:59.000Z

16

FLUORINATION OF OXIDIC NUCLEAR FUEL  

DOE Patents (OSTI)

A process of volatilizing fissionable material away from fission products, present together in neutron-bombarded uranium oxide, by reaction with an oxygen-fluorine mixture at 350 to 500 deg C is described. (AEC)

Mecham, W.J.; Gabor, J.D.

1963-07-23T23:59:59.000Z

17

It's Elemental - The Element Fluorine  

NLE Websites -- All DOE Office Websites (Extended Search)

Oxygen Oxygen Previous Element (Oxygen) The Periodic Table of Elements Next Element (Neon) Neon The Element Fluorine [Click for Isotope Data] 9 F Fluorine 18.9984032 Atomic Number: 9 Atomic Weight: 18.9984032 Melting Point: 53.53 K (-219.62°C or -363.32°F) Boiling Point: 85.03 K (-188.12°C or -306.62°F) Density: 0.001696 grams per cubic centimeter Phase at Room Temperature: Gas Element Classification: Non-metal Period Number: 2 Group Number: 17 Group Name: Halogen What's in a name? From the Latin and French words for flow, fluere. Say what? Fluorine is pronounced as FLU-eh-reen or as FLU-eh-rin. History and Uses: Fluorine is the most reactive of all elements and no chemical substance is capable of freeing fluorine from any of its compounds. For this reason, fluorine does not occur free in nature and was extremely difficult for

18

Method of preparing pure fluorine gas  

DOE Patents (OSTI)

A simple, inexpensive system for purifying and storing pure fluorine is described. The method utilizes alkali metal-nickel fluorides to absorb tank fluorine by forming nickel complex salts and leaving the gaseous impurities which are pumped away. The complex nickel fluoride is then heated to evolve back pure gaseous fluorine.

Asprey, Larned B. (Los Alamos, NM)

1976-01-01T23:59:59.000Z

19

Fluorination of Thermodynamically Unstable Nickel Fluorides ...  

... atoms at tertiary carbon sites in highly fluorinated molecules require the more powerful oxidizers, NiF 4 and NiF 3, for their oxidation. ...

20

Apparatus and Process for Production of Fluorine  

DOE Patents (OSTI)

Fluorine is produced by electrolyzing an acid potassium fluoride bath containing lithium fluoride with a copper impregnated carbon anode and a steel or iron cathode.

Whitaker, G.C.

1950-10-31T23:59:59.000Z

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


21

Copolymers of fluorinated polydienes and sulfonated polystyrene  

DOE Patents (OSTI)

Copolymers of fluorinated polydienes and sulfonated polystyrene and their use in fuel cell membranes, batteries, breathable chemical-biological protective materials, and templates for sol-gel polymerization.

Mays, Jimmy W. (Knoxville, TN); Gido, Samuel P. (Hadley, MA); Huang, Tianzi (Knoxville, TN); Hong, Kunlun (Knoxville, TN)

2009-11-17T23:59:59.000Z

22

Passivation of fluorinated activated charcoal  

SciTech Connect

The Molten Salt Reactor Experiment (MSRE), at the Oak Ridge National Laboratory has been shut down since 1969 when the fuel salt was drained from the core into two Hastelloy N tanks at the reactor site. In 1995, a multiyear project was launched to remediate the potentially hazardous conditions generated by the movement of fissile material and reactive gases from the storage tanks into the piping system and an auxiliary charcoal bed (ACB). The top 12 in. of the ACB is known by gamma scan and thermal analysis to contain about 2.6 kg U-233. According to the laboratory tests, a few feet of fluorinated charcoal are believed to extend beyond the uranium front. The remainder of the ACB should consist of unreacted charcoal. Fluorinated charcoal, when subjected to rapid heating, can decompose generating gaseous products. Under confined conditions, the sudden exothermic decomposition can produce high temperatures and pressures of near-explosive characteristics. Since it will be necessary to drill and tap the ACB to allow installation of piping and instrumentation for remediation and recovery activities, it is necessary to chemically convert the reactive fluorinated charcoal into a more stable material. Ammonia can be administered to the ACB as a volatile denaturing agent that results in the conversion of the C{sub x}F to carbon and ammonium fluoride, NH{sub 4}F. The charcoal laden with NH{sub 4}F can then be heated without risking any sudden decomposition. The only consequence of heating the treated material will be the volatilization of NH{sub 4}F as a mixture of NH{sub 3} and HF, which would primarily recombine as NH{sub 4}F on surfaces below 200 C. The planned scheme for the ACB denaturing is to flow diluted ammonia gas in steps of increasing NH{sub 3} concentration, 2% to 50%, followed by the injection of pure ammonia. This report summarizes the planned passivation treatment scheme to stabilize the ACB and remove the potential hazards. It also includes basic information, results of laboratory tests, thermodynamic calculations, process description, and operational parameters, and addresses safety concerns.

Del Cul, G.D.; Trowbridge, L.D.; Simmons, D.W.; Williams, D.F.; Toth, L.M.

1997-10-01T23:59:59.000Z

23

Super-hydrophobic fluorine containing aerogels  

Science Conference Proceedings (OSTI)

An aerogel material with surfaces containing fluorine atoms which exhibits exceptional hydrophobicity, or the ability to repel liquid water. Hydrophobic aerogels are efficient absorbers of solvents from water. Solvents miscible with water are separated from it because the solvents are more volatile than water and they enter the porous aerogel as a vapor across the liquid water/solid interface. Solvents that are immisicble with water are separated from it by selectively wetting the aerogel. The hydrophobic property is achieved by formulating the aerogel using fluorine containing molecules either directly by addition in the sol-gel process, or by treating a standard dried aerogel using the vapor of fluorine containing molecules.

Coronado, Paul R. (Livermore, CA); Poco, John F. (Livermore, CA); Hrubesh, Lawrence W. (Pleasanton, CA)

2007-05-01T23:59:59.000Z

24

Fluorination utilizing thermodynamically unstable fluorides and fluoride salts thereof  

DOE Green Energy (OSTI)

A method for fluorinating a carbon compound or cationic carbon compound utilizes a fluorination agent selected from thermodynamically unstable nickel fluorides and salts thereof in liquid anhydrous hydrogen fluoride. The desired carbon compound or cationic organic compound to undergo fluorination is selected and reacted with the fluorination agent by contacting the selected organic or cationic organic compound and the chosen fluorination agent in a reaction vessel for a desired reaction time period at room temperature or less.

Bartlett, Neil (Orinda, CA); Whalen, J. Marc (Corning, NY); Chacon, Lisa (Corning, NY)

2000-12-12T23:59:59.000Z

25

RECOVERY OF Pu VALUES BY FLUORINATION AND FRACTIONATION  

DOE Patents (OSTI)

A method is presented for the concentration and recovery of plutonium by fluorination and fractionation. A metallic mass containing uranium and plutonium is heated to 250 C and contacted with a stream of elemental fluorine. After fluorination of the metallic mass, the rcaction products are withdrawn and subjected to a distillation treatment to separate the fluorination products of uranium and to obtain a residue containing the fluorination products of plutonium.

Brown, H.S.; Webster, D.S.

1959-01-20T23:59:59.000Z

26

By-products from DU Storage (Fluorine and Empty Cylinders)  

NLE Websites -- All DOE Office Websites (Extended Search)

By-products from DU Storage By-products from DU Storage (Fluorine and Empty Cylinders) Potential applications involving by-products from DUF6 storage include fluorine applications...

27

Method for fluorination of uranium oxide  

SciTech Connect

Highly pure uranium hexafluoride is made from uranium oxide and fluorine. The uranium oxide, which includes UO.sub.3, UO.sub.2, U.sub.3 O.sub.8 and mixtures thereof, is introduced together with a small amount of a fluorine-reactive substance, selected from alkali chlorides, silicon dioxide, silicic acid, ferric oxide, and bromine, into a constant volume reaction zone. Sufficient fluorine is charged into the zone at a temperature below approximately 0.degree. C. to provide an initial pressure of at least approximately 600 lbs/sq. in. at the ambient atmospheric temperature. The temperature is then allowed to rise in the reaction zone until reaction occurs.

Petit, George S. (Oak Ridge, TN)

1987-01-01T23:59:59.000Z

28

Fluorinated diamond bonded in fluorocarbon resin  

SciTech Connect

By fluorinating diamond grit, the grit may be readily bonded into a fluorocarbon resin matrix. The matrix is formed by simple hot pressing techniques. Diamond grinding wheels may advantageously be manufactured using such a matrix. Teflon fluorocarbon resins are particularly well suited for using in forming the matrix.

Taylor, Gene W. (Los Alamos, NM)

1982-01-01T23:59:59.000Z

29

Fluorine compounds for doping conductive oxide thin films  

DOE Patents (OSTI)

Methods of forming a conductive fluorine-doped metal oxide layer on a substrate by chemical vapor deposition are described. The methods may include heating the substrate in a processing chamber, and introducing a metal-containing precursor and a fluorine-containing precursor to the processing chamber. The methods may also include adding an oxygen-containing precursor to the processing chamber. The precursors are reacted to deposit the fluorine-doped metal oxide layer on the substrate. Methods may also include forming the conductive fluorine-doped metal oxide layer by plasma-assisted chemical vapor deposition. These methods may include providing the substrate in a processing chamber, and introducing a metal-containing precursor, and a fluorine-containing precursor to the processing chamber. A plasma may be formed that includes species from the metal-containing precursor and the fluorine-containing precursor. The species may react to deposit the fluorine-doped metal oxide layer on the substrate.

Gessert, Tim; Li, Xiaonan; Barnes, Teresa M; Torres, Jr., Robert; Wyse, Carrie L

2013-04-23T23:59:59.000Z

30

Immobilization of iodine in concrete  

DOE Patents (OSTI)

A method for immobilizing fission product radioactive iodine recovered from irradiated nuclear fuel comprises combining material comprising water, Portland cement and about 3-20 wt. % iodine as Ba(IO.sub.3).sub.2 to provide a fluid mixture and allowing the fluid mixture to harden, said Ba(IO.sub.3).sub.2 comprising said radioactive iodine. An article for solid waste disposal comprises concrete prepared by this method. BACKGROUND OF THE INVENTION This invention was made in the course of, or under a contract with the Energy Research and Development Administration. It relates in general to reactor waste solidification and more specifically to the immobilization of fission product radioactive iodine recovered from irradiated nuclear fuel for underground storage.

Clark, Walter E. (Oak Ridge, TN); Thompson, Clarence T. (Oak Ridge, TN)

1977-04-12T23:59:59.000Z

31

Microsoft PowerPoint - 2012 Pyro Conf Iodine Partitioning 2  

NLE Websites -- All DOE Office Websites (Extended Search)

in EBR-II Fuel Iodine Off-gas During Pyroprocessing Iodine off-gas during salt distillation operations Iodine off-gas during ceramic waste form production Iodine Off-gas...

32

A Nuclear Reaction Analysis study of fluorine uptake in flint  

SciTech Connect

Nuclear Reaction Analysis (NRA) using the {sup 19}F(p,{alpha}{gamma}){sup 16}O resonance reaction is a powerful method of fluorine depth profiling. We have used this method to study the fluorine uptake phenomenon in mineral flint, which could potentially develop into a method of dating archeological flint artifacts. Flint samples cut with a rock saw were immersed in aqueous fluoride solutions for different times for the uptake study. The results suggest that fluorine uptake is not a simple phenomenon, but rather a combination of several simultaneous processes. Fluorine surface adsorption appears to play an important role in developing the fluorine profiles. The surface adsorption was affected by several parameters such as pH value and fluorine concentration in the solution, among others. The problem of surface charging for the insulator materials during ion bombardment is also reported.

Jin, Jian-Yue; Weathers, D. L.; Picton, F.; Hughes, B. F.; Duggan, J. L.; McDaniel, F. D.; Matteson, S. [Ion Beam Modification and Analysis Laboratory (IBMAL), Department of Physics, University of North Texas, Denton, Texas 76203 (United States)

1999-06-10T23:59:59.000Z

33

Fluorinated Arylboron Oxalate for Non-Aqueous Battery Electrolytes  

A range of new fluorinated arylboron oxalate compounds for use as additives and anion receptors in lithium-based battery electrolytes have been ...

34

It's Elemental - The Element Iodine  

NLE Websites -- All DOE Office Websites (Extended Search)

Tellurium Tellurium Previous Element (Tellurium) The Periodic Table of Elements Next Element (Xenon) Xenon The Element Iodine [Click for Isotope Data] 53 I Iodine 126.90447 Atomic Number: 53 Atomic Weight: 126.90447 Melting Point: 386.85 K (113.7°C or 236.7°F) Boiling Point: 457.55 K (184.4°C or 364.0°F) Density: 4.93 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Non-metal Period Number: 5 Group Number: 17 Group Name: Halogen What's in a name? From the Greek word for violet, iodes. Say what? Iodine is pronounced as EYE-eh-dine or as EYE-eh-din. History and Uses: Iodine was discovered by the French chemist Barnard Courtois in 1811. Courtois was extracting sodium and potassium compounds from seaweed ash. Once these compounds were removed, he added sulfuric acid (H2SO4) to

35

Fluorine gettering by activated charcoal in a radiation environment  

SciTech Connect

Activated charcoal has been shown to be an effective gettering agent for the fluorine gas that is liberated in a radiation environment. Even though activated charcoal is a commonly used getter, little is known about the radiation stability of the fluorine-charcoal product. This work has shown that not only is the product stable in high gamma radiation fields, but also that radiation enhances the capacity of the charcoal for the fluorine. The most useful application of this work is with the Molten Salt Reactor Experiment (MSRE) fuel salt because the radioactive components (fission products and actinides) cause radiolytic damage to the solid LiF-BeF/sub 2/-ZrF/sub 4/-UF/sub 4/ (64.5, 30.3, 5.0, 0.13 mol %, respectively) resulting in the liberation of fluorine gas. This work has also demonstrated that the maximum damage to the fuel salt by approx.3 /times/ 10/sup 7/ R/h gamma radiation is approximately 2%, at which point the rate of recombination of fluorine with active metal sites within the salt lattice equals the rate of fluorine generation. The enhanced reactivity of the activated charcoal and radiation stability of the product ensures that the gettered fluorine will stay sequestered in the charcoal.

Felker, L.K.; Toth, L.M.

1988-10-01T23:59:59.000Z

36

Method for directly recovering fluorine from gas streams  

DOE Patents (OSTI)

This invention is a process for the direct recovery of gaseous fluorine from waste-gas streams or the like. The process comprises passing the gas stream through a bed of anhydrous K.sub.3 NiF.sub.6 pellets to fluorinate the same to K.sub.3 NiF.sub.7 and subsequently desorbing the fluorine by heating the K.sub.3 NiF.sub.7 pellets to a temperature re-converting them to K.sub.3 NiF.sub.6. The efficiency of the fluorine-absorption step is maximized by operating in a selected and conveniently low temperature. The desorbed fluorine is highly pure and is at a pressure of several atmospheres. Preferably, the K.sub.3 NiF.sub.6 pellets are prepared by a method including the steps of forming agglomerates of hydrated K.sub.3 NiF.sub.5, sintering the agglomerates to form K.sub.3 NiF.sub.5 pellets of enhanced reactivity with respect to fluorine, and fluorinating the sintered pellets to K.sub.3 NiF.sub.6.

Orlett, Michael J. (Portsmouth, OH); Saraceno, Anthony J. (Waverly, OH)

1981-01-01T23:59:59.000Z

37

Iodine Stabilized Helium-Neon Laser  

Science Conference Proceedings (OSTI)

... stabilized lasers or spectral lamps that have been recommended for use by international consensus. The iodine stabilized helium-neon laser is just ...

38

A LABORATORY INVESTIGATION OF THE FLUORINATION OF CRUDE URANIUM TETRAFLUORIDE  

DOE Green Energy (OSTI)

Ore concentrates were converted directly to crude uranium tetrafluoride by hydrogen reduction aad hydrofluorination in fluidized-bed reactors. Small- scale laboratory experiments demonstrated that this process can be extended to the production of crude uranium hexafluoride through fluorination of the uranium tetrafluoride in a fluidized bed. The satisfactory temperature range for the reaction lies between 300 and 600 deg C. At 450 deg C the fluorine utilization is between 50 and 80%. With excess fluorine, over 99% of the uranium is volatilized from the solid material. The fluidization characteristics of certain materials are improved by the addition of an inert solid diluent to the bed. (auth) .

Sandus, O.; Steunenberg, R.K.

1957-12-01T23:59:59.000Z

39

Dry process fluorination of uranium dioxide using ammonium bifluoride  

E-Print Network (OSTI)

An experimental study was conducted to determine the practicality of various unit operations for fluorination of uranium dioxide. The objective was to prepare ammonium uranium fluoride double salts from uranium dioxide and ...

Yeamans, Charles Burnett, 1978-

2003-01-01T23:59:59.000Z

40

Fluorination of amorphous thin-film materials with xenon fluoride  

DOE Patents (OSTI)

A method is disclosed for producing fluorine-containing amorphous semiconductor material, preferably comprising amorphous silicon. The method includes depositing amorphous thin-film material onto a substrate while introducing xenon fluoride during the film deposition process.

Weil, Raoul B. (Haifa, IL)

1988-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


41

Iodine transport analysis in the ESBWR.  

Science Conference Proceedings (OSTI)

A simplified ESBWR MELCOR model was developed to track the transport of iodine released from damaged reactor fuel in a hypothesized core damage accident. To account for the effects of iodine pool chemistry, radiolysis of air and cable insulation, and surface coatings (i.e., paint) the iodine pool model in MELCOR was activated. Modifications were made to MELCOR to add sodium pentaborate as a buffer in the iodine pool chemistry model. An issue of specific interest was whether iodine vapor removed from the drywell vapor space by the PCCS heat exchangers would be sequestered in water pools or if it would be rereleased as vapor back into the drywell. As iodine vapor is not included in the deposition models for diffusiophoresis or thermophoresis in current version of MELCOR, a parametric study was conducted to evaluate the impact of a range of iodine removal coefficients in the PCCS heat exchangers. The study found that higher removal coefficients resulted in a lower mass of iodine vapor in the drywell vapor space.

Kalinich, Donald A.; Gauntt, Randall O.; Young, Michael Francis; Longmire, Pamela

2009-03-01T23:59:59.000Z

42

Method for immobilizing radioactive iodine  

DOE Patents (OSTI)

Radioactive iodine, present as alkali metal iodides or iodates in an aqueous solution, is incorporated into an inert solid material for long-term storage by adding to the solution a stoichiometric amount with respect to the formation of a sodalite (3M.sub.2 O.3Al.sub.2 O.sub.3. 6SiO.sub.2.2MX, where M=alkali metal; X=I.sup.- or IO.sub.3.sup.-) of an alkali metal, alumina and silica, stirring the solution to form a homogeneous mixture, drying the mixture to form a powder, compacting and sintering the compacted powder at 1073 to 1373 K (800.degree. to 1100.degree. C.) for a time sufficient to form sodalite.

Babad, Harry (Richland, WA); Strachan, Denis M. (Richland, WA)

1980-01-01T23:59:59.000Z

43

Mixed-layered bismuth-oxygen-iodine materials for capture and waste disposal of radioactive iodine  

DOE Patents (OSTI)

Materials and methods of synthesizing mixed-layered bismuth oxy-iodine materials, which can be synthesized in the presence of aqueous radioactive iodine species found in caustic solutions (e.g. NaOH or KOH). This technology provides a one-step process for both iodine sequestration and storage from nuclear fuel cycles. It results in materials that will be durable for repository conditions much like those found in Waste Isolation Pilot Plant (WIPP) and estimated for Yucca Mountain (YMP). By controlled reactant concentrations, optimized compositions of these mixed-layered bismuth oxy-iodine inorganic materials are produced that have both a high iodine weight percentage and a low solubility in groundwater environments.

Krumhansl, James L; Nenoff, Tina M

2013-02-26T23:59:59.000Z

44

RECOVERY OF Pu FROM CERIUM TRIFLUORIDE BY FLUORINATION  

DOE Patents (OSTI)

An improved process is prcsented for selectively recovering plutonium from a solution containing fission products comprising precipitating cerium trifluoride in the solution for effccting carrier precipitation of plutonium. The resulting carrier precipitate is dried and subjected to fluorination at about 600 C. The plutonium forms a volatile fiuoridc and is so separated from the nonvolatile cerium fluoride.

Brown, H.S.; Bohlmann, E.G.

1959-02-10T23:59:59.000Z

45

Dry method for recycling iodine-loaded silver zeolite  

DOE Green Energy (OSTI)

Fission product iodine is removed from a waste gas stream and stored by passing the gas stream through a bed of silver-exchanged zeolite until the zeolite is loaded with iodine, passing dry hydrogen gas through the bed to remove the iodine and regenerate the bed, and passing the hydrogen stream containing the hydrogen iodide thus formed through a lead-exchanged zeolite which adsorbs the radioactive iodine from the gas stream and permanently storing the lead-exchanged zeolite loaded with radioactive iodine.

Thomas, Thomas R. (Idaho Falls, ID); Staples, Bruce A. (Idaho Falls, ID); Murphy, Llewellyn P. (Idaho Falls, ID)

1978-05-09T23:59:59.000Z

46

Iodine retention during evaporative volume reduction  

DOE Patents (OSTI)

An improved method for retaining radioactive iodine in aqueous waste solutions during volume reduction is disclosed. The method applies to evaporative volume reduction processes whereby the decontaminated (evaporated) water can be returned safely to the environment. The method generally comprises isotopically diluting the waste solution with a nonradioactive iodide and maintaining the solution at a high pH during evaporation.

Godbee, H.W.; Cathers, G.I.; Blanco, R.E.

1975-11-18T23:59:59.000Z

47

Fluorinated diamond particles bonded in a filled fluorocarbon resin matrix  

DOE Patents (OSTI)

A method of producing fluorinated diamond particles bonded in a filled fluorocarbon resin matrix. Simple hot pressing techniques permit the formation of such matrices from which diamond impregnated grinding tools and other articles of manufacture can be produced. Teflon fluorocarbon resins filled with Al/sub 2/O/sub 3/ yield grinding tools with substantially improved work-to-wear ratios over grinding wheels known in the art.

Taylor, G.W.; Roybal, H.E.

1983-11-14T23:59:59.000Z

48

Iodine Revolatilization in a Grand Gulf Loca  

SciTech Connect

The TRENDS models are applied at each time step to each control volume. Significant amounts of water occur only in the wetwell and drywell sump (the refueling pool is not a factor, as discussed earlier). In Fig. 2, we show the radiolytic acid production feeding into each of these pools. Since the water is initially neutral and no chemical additives are present, the acid additions are the major factors affecting pH. In Fig. 3, we see the downward trend of pH resulting from these acid additions. The conversion of iodide (I{sup {minus}}) to molecular iodine (I{sub 2}) is most noticeable in the wetwell, since this is the repository of most iodide and HCl. Gradually, during the transient small amounts of more volatile iodine are formed. While iodide remains the dominant form, noticeable amounts of I{sub 2} and intermediate species are created. Once produced in water, some I{sub 2} is free to evaporate into airspace. Fig. 4 indicates the increase in all airborne iodine throughout the transient. This is compared to the MELCOR result for CsI aerosol, which decreases dramatically due to containment sprays. The I{sub 2} in the airspace can be vented to the enclosure building or the environment. In the present accident sequence, the only path to the environment was through the SGTS, which was assumed to operate as in MELCOR. However, both are dwarfed by the MELCOR gaseous release during the first 12 h because MELCOR does not model spray washout of gaseous iodine. Steadily increasing throughout the transient, the revolatilization release is eventually more than an order-or-magnitude higher than the MELCOR aerosol release. Also, 99% of iodine flowing directly through the SGTS was retained in filters. The remaining 1% was released to the environment. In addition, a small flow bypassing the SGTS filters vented directly into the environment. The total released from these two paths is shown in Fig. 5.

Beahm, E.C.; Weber, C.F.

1999-01-01T23:59:59.000Z

49

Fluorinated precursors of superconducting ceramics, and methods of making the same  

DOE Patents (OSTI)

This invention provides a method of making a fluorinated precursor of a superconducting ceramic. The method comprises providing a solution comprising a rare earth salt, an alkaline earth metal salt and a copper salt; spraying the solution onto a substrate to provide a film-covered substrate; and heating the film-covered substrate in an atmosphere containing fluorinated gas to provide the fluorinated precursor.

Wiesmann, Harold (Stony Brook, NY); Solovyov, Vyacheslav (Rocky Point, NY)

2008-04-22T23:59:59.000Z

50

Fluorinated precursors of superconducting ceramics, and methods of making the same  

SciTech Connect

This invention provides a method of making a fluorinated precursor of a superconducting ceramic. The method comprises providing a solution comprising a rare earth salt, an alkaline earth metal salt and a copper salt; spraying the solution onto a substrate to provide a film-covered substrate; and heating the film-covered substrate in an atmosphere containing fluorinated gas to provide the fluorinated precursor.

Wiesmann, Harold (Stony Brook, NY); Solovyov, Vyacheslav (Rocky Point, NY)

2012-07-10T23:59:59.000Z

51

Effect of radical fluorination on mono- and bi-layer graphene in Ar/F{sub 2} plasma  

SciTech Connect

Fluorinated graphene has the possibility to achieve unique properties and functions in graphene. We propose a highly controlled fluorination method utilizing fluorine radicals in Ar/F{sub 2} plasma. To suppress ion bombardments and improve the reaction with fluorine radicals on graphene, the substrate was placed 'face down' in the plasma chamber. Although monolayer graphene was more reactive than bilayer, fluorination of bilayer reached the level of I{sub D}/I{sub G} {approx} 0.5 in Raman D peak intensity at 532 nm excitation. Annealing fluorinated samples proved reversibility of radical fluorination for both mono- and bi-layer graphenes. X-ray photoelectron spectroscopy showed the existence of carbon-fluorine bonding.

Tahara, K.; Iwasaki, T.; Hatano, M. [Department of Physical Electronics, Tokyo Institute of Technology, Tokyo 152-8552 (Japan); Matsutani, A. [Semiconductor and MEMS Processing Center, Technical Department, Tokyo Institute of Technology, Tokyo 226-8503 (Japan)

2012-10-15T23:59:59.000Z

52

Radioactive iodine therapy in cats with hyperthyroidism  

SciTech Connect

Eleven cats with hyperthyroidism were treated with radioactive iodine (/sup 131/I). Previous unsuccessful treatments for hyperthyroidism included hemithyroidectomy (2 cats) and an antithyroid drug (7 cats). Two cats had no prior treatment. Thyroid scans, using technetium 99m, showed enlargement and increased radionuclide accumulation in 1 thyroid lobe in 5 cats and in both lobes in 6 cats. Serum thyroxine concentrations were high and ranged from 4.7 to 18 micrograms/dl. Radioactive iodine tracer studies were used to determine peak radioactive iodine uptake (RAIU) and effective and biological half-lives. Activity of /sup 131/I administered was calculated from peak RAIU, effective half-life, and estimated thyroid gland weight. Activity of /sup 131/I administered ranged from 1.0 to 5.9 mCi. The treatment goal was to deliver 20,000 rad to hyperactive thyroid tissue. However, retrospective calculations based on peak RAIU and effective half-life obtained during the treatment period showed that radiation doses actually ranged from 7,100 to 64,900 rad. Complete ablation of the hyperfunctioning thyroid tissue and a return to euthyroidism were seen in 7 cats. Partial responses were seen in 2 cats, and 2 cats became hypothyroid. It was concluded that /sup 131/I ablation of thyroid tumors was a reasonable alternative in the treatment of hyperthyroidism in cats. The optimal method of dosimetry remains to be determined.

Turrel, J.M.; Feldman, E.C.; Hays, M.; Hornof, W.J.

1984-03-01T23:59:59.000Z

53

Efforts to Consolidate Chalcogels with Adsorbed Iodine  

Science Conference Proceedings (OSTI)

This document discusses ongoing work with non-oxide aerogels, called chalcogels, that are under development at the Pacific Northwest National Laboratory as sorbents for gaseous iodine. Work was conducted in fiscal year 2012 to demonstrate the feasibility of converting Sn2S3 chalcogel without iodine into a glass. This current document summarizes the work conducted in fiscal year 2013 to assess the consolidation potential of non-oxide aerogels with adsorbed iodine. The Sn2S3 and Sb13.5Sn5S20 chalcogels were selected for study. The first step in the process for these experiments was to load them with iodine (I2). The I2 uptake was ~68 mass% for Sn2S3 and ~50 mass% for Sb13.5Sn5S20 chalcogels. X-ray diffraction (XRD) of both sets of sorbents showed that metal-iodide complexes were formed during adsorption, i.e., SnI4 for Sn2S3 and SbI3 for Sb13.5Sn5S20. Additionally, metal-sulfide-iodide complexes were formed, i.e., SnSI for Sn2S3 and SbSI for Sb13.5Sn5S20. No XRD evidence for unreacted iodine was found in any of these samples. Once the chalcogels had reached maximum adsorption, the consolidation potential was assessed. Here, the sorbents were heated for consolidation in vacuum-sealed quartz vessels. The Sb13.5Sn5S20 chalcogel was heated both (1) in a glassy carbon crucible within a fused quartz tube and (2) in a single-containment fused quartz tube. The Sn2S3 chalcogel was only heated in a single-containment fused quartz tube. In both cases with the single-containment fused quartz experiments, the material consolidated nicely. However, in both cases, there were small fractions of metal iodides not incorporated into the final product as well as fused quartz particles within the melt due to the sample attacking the quartz wall during the heat treatment. The Sb13.5Sn5S20 did not appear to attack the glassy carbon crucible so, for future experiments, it would be ideal to apply a coating, such as pyrolytic graphite, to the inner walls of the fused quartz vessel to prevent melt attack.

Riley, Brian J.; Pierce, David A.; Chun, Jaehun

2013-08-28T23:59:59.000Z

54

Sulfur-Iodine thermochemical cycle for hydrogen production.  

E-Print Network (OSTI)

??The aim of the thesis was to study the Sulfur-Iodine thermochemical cycle for hydrogen production. There were three reactions in this cycle: Bunsen reaction, sulfuric… (more)

Dan, Huang

2009-01-01T23:59:59.000Z

55

Method for gettering organic, inorganic and elemental iodine in aqueous solutions  

SciTech Connect

A process for the removal of iodine from aqueous solutions, particularly the trapping of radioactive iodine to mitigate damage resulting from accidents or spills associated with nuclear reactors, by exposing the solution to well dispersed silver carbonate which reacts with the iodine and iodides, thereby gettering iodine and iodine compounds from solution. The iodine is not only removed from solution but also from the contiguous vapor.

Beahm, Edward C. (Oak Ridge, TN); Shockley, William E. (Oak Ridge, TN)

1990-01-01T23:59:59.000Z

56

Stripes of Partially Fluorinated Alkyl Chains: Dipolar Langmuir Monolayers  

E-Print Network (OSTI)

Stripe-like domains of Langmuir monolayers formed by surfactants with partially fluorinated lipid anchors (F-alkyl lipids) are observed at the gas-liquid phase coexistence. The average periodicity of the stripes, measured by fluorescence microscopy, is in the micrometer range, varying between 2 and 8 microns. The observed stripe-like patterns are stabilized due to dipole-dipole interactions between terminal -CF3 groups. These interactions are particularly strong as compared with non-fluorinated lipids due to the low dielectric constant of the surrounding media (air). These long-range dipolar interactions tend to elongate the domains, in contrast to the line tension that tends to minimize the length of the domain boundary. This behavior should be compared with that of the lipid monolayer having alkyl chains, and which form spherical micro-domains (bubbles) at the gas-liquid coexistence. The measured stripe periodicity agrees quantitatively with a theoretical model. Moreover, the reduction in line tension by adding traces (0.1 mol fraction) of cholesterol results, as expected, in a decrease in the domain periodicity.

Matthias F. Schneider; David Andelman; Motomu Tanaka

2005-01-16T23:59:59.000Z

57

BEDT-TFF salts with fluorinated sulfonate anions.  

Science Conference Proceedings (OSTI)

A number of layered conducting BEDT-TTF, bis(ethylenedithio)tetrathiafulvalene, salts with heavily fluorinated organosulfonate anions have been prepared and characterized. Of particular interest are the salts containing SF{sub 5}RSO{sub 3}{sup -} anions, where R is a partially fluorinated aliphatic backbone. While structurally similar --the {beta}' packing type predominates--the ground state of these salts varies from superconducting in the case of {beta}'-(BEDT-TTF){sub 2}SF{sub 5}CH{sub 2}CF{sub 2}SO{sub 3} [1] to insulating. Many of the salts with insulating ground states are metallic at room temperature, but charge localization and disproportionation over crystallographically non-equivalent sites occurs at low temperature. The organosulfonate group exhibits a propensity to bind to lithium ions, thus ternary salts incorporating Li+ into the complex anion layer are often found. The fluorophilic effect in organofluorine compounds may be exploited to form salts where the conducting BEDT-TTF layers are separated by extremely bulky anion bilayers. The crystal structure of one such system, (BEDT-TTF){sub 3}[(CF{sub 3}){sub 2}CFC{sub 2}H{sub 4}SO{sub 3}]{sub 4}(H{sub 5}O{sub 2}){sub 2}, is described here.

Geiser, U.; Schlueter, J. A.; Kini, A. M.; Wang, H. H.; Ward, B. H.; Mohtasham, J.; Gard, G. L.; Portland State Univ.

2003-01-01T23:59:59.000Z

58

Iodine Sorbent Performance in FY 2012 Deep Bed Tests  

SciTech Connect

Nuclear fission results in the production of fission products and activation products, some of which tend to be volatile during used fuel reprocessing and evolve in gaseous species into the reprocessing facility off-gas systems. Analyses have shown that I-129, due to its radioactivity, high potential mobility in the environment, and high longevity (half life of 15.7 million years), can require control efficiencies of up to 1,000x or higher to meet regulatory emission limits. Iodine capture is an important aspect of the Separations and Waste Forms Campaign Off-gas Sigma Team (Jubin 2011, Pantano 2011). Deep-bed iodine sorption tests for both silver-functionalized Aerogel and silver zeolite sorbents were performed during Fiscal Year 2012. These tests showed that: • Decontamination factors were achieved that exceed reasonably conservative estimates for DFs needed for used fuel reprocessing facilities in the U.S. to meet regulatory requirements for I-129 capture. • Silver utilizations approached or exceeded 100% for high inlet gas iodine concentrations, but test durations were not long enough to approach 100% silver utilization for lower iodine concentrations. • The depth of the mass transfer zone was determined for both low iodine concentrations (under 10 ppmv) and for higher iodine concentrations (between 10-50 ppmv); the depth increases over time as iodine is sorbed. • These sorbents capture iodine by chemisorption, where the sorbed iodine reacts with the silver to form very non-volatile AgI. Any sorbed iodine that is physisorbed but not chemically reacted with silver to form AgI might not be tightly held by the sorbent. The portion of sorbed iodine that tends to desorb because it is not chemisorbed (reacted to form AgI) is small, under 1%, for the AgZ tests, and even smaller, under 0.01%, for the silver-functionalized Aerogel.

Nick Soelberg; Tony Watson

2012-08-01T23:59:59.000Z

59

Uranium mineralization in fluorine-enriched volcanic rocks  

Science Conference Proceedings (OSTI)

Several uranium and other lithophile element deposits are located within or adjacent to small middle to late Cenozoic, fluorine-rich rhyolitic dome complexes. Examples studied include Spor Mountain, Utah (Be-U-F), the Honeycomb Hills, Utah (Be-U), the Wah Wah Mountains, Utah (U-F), and the Black Range-Sierra Cuchillo, New Mexico (Sn-Be-W-F). The formation of these and similar deposits begins with the emplacement of a rhyolitic magma, enriched in lithophile metals and complexing fluorine, that rises to a shallow crustal level, where its roof zone may become further enriched in volatiles and the ore elements. During initial explosive volcanic activity, aprons of lithicrich tuffs are erupted around the vents. These early pyroclastic deposits commonly host the mineralization, due to their initial enrichment in the lithophile elements, their permeability, and the reactivity of their foreign lithic inclusions (particularly carbonate rocks). The pyroclastics are capped and preserved by thick topaz rhyolite domes and flows that can serve as a source of heat and of additional quantities of ore elements. Devitrification, vapor-phase crystallization, or fumarolic alteration may free the ore elements from the glassy matrix and place them in a form readily leached by percolating meteoric waters. Heat from the rhyolitic sheets drives such waters through the system, generally into and up the vents and out through the early tuffs. Secondary alteration zones (K-feldspar, sericite, silica, clays, fluorite, carbonate, and zeolites) and economic mineral concentrations may form in response to this low temperature (less than 200 C) circulation. After cooling, meteoric water continues to migrate through the system, modifying the distribution and concentration of the ore elements (especially uranium).

Burt, D.M.; Sheridan, M.F.; Bikun, J.; Christiansen, E.; Correa, B.; Murphy, B.; Self, S.

1980-09-01T23:59:59.000Z

60

AGING AND IODINE LOADING OF SILVER-FUNCTIONALIZED AEROGELS  

SciTech Connect

Engineered silver-functionalized silica aerogels are being investigated for their application in off-gas treatment at a used nuclear fuel reprocessing facility. Reprocessing will release several key volatile radionuclides, including iodine-129. To achieve regulatory compliance, iodine-129 must be removed from any off-gas stream prior to environmental discharge. Silver-functionalized aerogels have been demonstrated to have high iodine capture capacity, high porosity and potential for conversion into a waste form. Capture materials used in off-gas treatment may be exposed to a heated, high humidity, acidic gas stream for months. Extended exposure to this stream could affect sorbent performance. It was the aim of this study to evaluate what impacts might be observed when Ag0-functionalized aerogels prepared at Pacific Northwest National Laboratory were contacted with a dry air stream for up to 6 months and then used to adsorb iodine from a synthetic off-gas stream. Results demonstrate that there is some loss of iodine capture capacity caused by aging, but that this loss is not as marked as for aging of more traditional iodine sorbents, such as silver-impregnated mordenite. Specifically, aging silver-functionalized aerogel under a dry air stream for up to 6 months can decrease its iodine capacity from 41wt% to 32wt%.

Bruffey, Stephanie H [ORNL; Jubin, Robert Thomas [ORNL; Anderson, Kaara K [ORNL; Walker Jr, Joseph Franklin [ORNL

2013-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


61

Significantly improved piezoelectric thermal stability of cellular polypropylene films by high pressure fluorination and post-treatments  

Science Conference Proceedings (OSTI)

Cellular polypropylene (PP) films were fluorinated under a high pressure of 13 bar of the F{sub 2}/N{sub 2} mixture and were post-treated by nitrous oxide and isothermal crystallization. The fluorinated and post-treated PP films after being expanded and corona charged exhibit a significantly improved piezoelectric thermal stability. After annealing at 70 deg. C for 151 h or at 90 deg. C for 224 h, the piezoelectric d{sub 33} value of the fluorinated and post-treated piezoelectric sample still retains 58% or 45% of its initial d{sub 33} value, while the corresponding value of the virgin piezoelectric sample has decreased to 29% or 15% of the initial value. Chemical composition analysis of the cross section of the fluorinated and post-treated film by energy-dispersive x-ray spectroscopy indicates that the internal layers have been fluorinated, in spite of a lower degree of fluorination compared with the fluorinated surface layer. Short-circuit and open-circuit TSD current measurements reveal that the fluorinated internal layers, like the fluorinated surface layer, also have very deep charge traps, although there probably is a difference in density of the deep traps between them. The deeply trapped charge on the internal layers of the fluorinated and post-treated piezoelectric sample is responsible for its significantly improved piezoelectric thermal stability.

An Zhenlian [Ministry of Education Key Laboratory of Advanced Microstructure Materials, Department of Physics, Tongji University, 1239 Siping Road, Shanghai 200092 (China); State Key Laboratory of Electrical Insulation and Power Equipment, Xi'an Jiaotong University, 28 Xianning West Road, Xi'an 710049 (China); Mao Mingjun; Cang Jun; Zhang Yewen; Zheng Feihu [Ministry of Education Key Laboratory of Advanced Microstructure Materials, Department of Physics, Tongji University, 1239 Siping Road, Shanghai 200092 (China)

2012-01-15T23:59:59.000Z

62

Method of extracting iodine from liquid mixtures of iodine, water and hydrogen iodide  

DOE Green Energy (OSTI)

The components of a liquid mixture consisting essentially of HI, water and at least about 50 w/o iodine are separated in a countercurrent extraction zone by treating with phosphoric acid containing at least about 90 w/o H.sub.3 PO.sub.4. The bottom stream from the extraction zone is substantially completely molten iodine, and the overhead stream contains water, HI, H.sub.3 PO.sub.4 and a small fraction of the amount of original iodine. When the water and HI are present in near-azeotropic proportions, there is particular advantage in feeding the overhead stream to an extractive distillation zone wherein it is treated with additional concentrated phosphoric acid to create an anhydrous HI vapor stream and bottoms which contain at least about 85 w/o H.sub.3 PO.sub.4. Concentration of these bottoms provides phosphoric acid infeed for both the countercurrent extraction zone and for the extractive distillation zone.

Mysels, Karol J. (La Jolla, CA)

1979-01-01T23:59:59.000Z

63

PLATINUM HEXAFLUORIDE AND METHOD OF FLUORINATING PLUTONIUM CONTAINING MIXTURES THERE-WITH  

DOE Patents (OSTI)

The preparation of platinum hexafluoride and its use as a fluorinating agent in a process for separating plutonium from fission products is presented. According to the invention, platinum is reacted with fluorine gas at from 900 to 1100 deg C to form platinum hexafluoride. The platinum hexafluoride is then contacted with the plutonium containing mixture at room temperature to form plutonium hexafluoride which is more volatile than the fission products fluorides and therefore can be isolated by distillation.

Malm, J.G.; Weinstock, B.; Claassen, H.H.

1959-07-01T23:59:59.000Z

64

Electron-collision cross sections for iodine  

Science Conference Proceedings (OSTI)

We present results from a joint experimental and theoretical study of elastic electron scattering from atomic iodine. The experimental results were obtained by subtracting known cross sections from the measured data obtained with a pyrolyzed mixed beam containing a variety of atomic and molecular species. The calculations were performed using both a fully relativistic Dirac B-spline R-matrix (close-coupling) method and an optical model potential approach. Given the difficulty of the problem, the agreement between the two sets of theoretical predictions and the experimental data for the angle-differential and the angle-integrated elastic cross sections at 40 eV and 50 eV is satisfactory.

Zatsarinny, O.; Bartschat, K. [Department of Physics and Astronomy, Drake University, Des Moines, Iowa 50311 (United States); Garcia, G. [Instituto de Fisica Fundamental, Consejo Superior de Investigaciones Cientificas, Madrid E-28006 (Spain); Blanco, F. [Departamento de Fisica Atomica, Molecular y Nuclear, Universidad Complutense de Madrid, Madrid E-28040 (Spain); Hargreaves, L.R.; Jones, D.B.; Murrie, R.; Brunton, J.R. [ARC Centre for Antimatter-Matter Studies, School of Chemical and Physical Sciences, Flinders University, GPO Box 2100, Adelaide, SA 5001 (Australia); Brunger, M.J. [ARC Centre for Antimatter-Matter Studies, School of Chemical and Physical Sciences, Flinders University, GPO Box 2100, Adelaide, SA 5001 (Australia); Institute of Mathematical Sciences, University of Malaya, 50603, Kuala Lumpur (Malaysia); Hoshino, M. [Department of Materials and Life Sciences, Sophia University, Chiyoda ku, Tokyo 102-8554 (Japan); Buckman, S.J. [ARC Centre for Antimatter-Matter Studies, Research School of Physics and Engineering, Australian National University, Canberra, ACT 0200 (Australia)

2011-04-15T23:59:59.000Z

65

Separation of iodine from mercury containing scrubbing solutions  

DOE Patents (OSTI)

Radioactive iodines can be recovered from a nitric acid scrub solution containing mercuric nitrate by passing a current through the scrub solution to react the iodine with the mercuric nitrate to form mercuric iodate which precipitates out. The mercuric iodate can then be reacted to recover the radioiodine for further processing into a form suitable for long-term storage and to recover the mercury for recycling.

Burger, Leland L. (Richland, WA); Scheele, Randall D. (Kennewick, WA)

1979-01-01T23:59:59.000Z

66

Recycle of iodine-loaded silver mordenite by hydrogen reduction  

SciTech Connect

In 1977 and 1978, workers at Idaho National Engineering Laboratory (INEL) developed and tested a process for the regeneration and reuse of silver mordenite, AgZ, used to trap iodine from the dissolver off-gas stream of a nuclear fuel reprocessing plant. We were requested by the Airborne Waste Management Program Office of the Department of Energy to perform a confirmatory recycle study using repeated loadings at about 150/sup 0/C with elemental iodine, each followed by a drying step at 300/sup 0/C, then by iodine removal using elemental hydrogen at 500/sup 0/C. The results of our study show that AgZ can be recycled. There was considerable difficulty in stripping the iodine at 500/sup 0/C.; however, this step went reasonably well at 550/sup 0/C or slightly higher, with no apparent loss in the iodine-loading capacity of the AgZ. Large releases of elemental iodine occurred during the drying stage and the early part of the stripping stage. Lead zeolite, which was employed in the original design to trap the HI produced, is ineffective in removal of I/sub 2/. The process needs modification to handle the iodine. Severe corrosion of the stainless steel components of the system resulted from the HI-I/sub 2/-H/sub 2/O mixture. Monel or other halogen-resistant materials need to be examined for this application. Because of difficulty with the stripping stage and with corrosion, the experiments were terminated after 12 cycles. Thus, the maximum lifetime (cycles) of recycle AgZ has not been determined. Mechanistic studies of iodine retention by silver zeolites and of the behavior of silver atoms on the reduction stage would be of assistance in optimizing silver mordenite recycle.

Burger, L.L.; Scheele, R.D.

1982-11-01T23:59:59.000Z

67

Selection of a form for fixation of iodine-129  

Science Conference Proceedings (OSTI)

This report summarizes work on the selection of an /sup 129/I disposal form. Iodine compounds have been screened on the basis of solubilities, thermal stabilities, cost and availability, toxicity of the cation, and the thermodynamic resistance to oxidation and hydrolysis, and leaching of that compound in portland type III cement. Also considered were iodine capture technology, disposal criteria or guidelines, and the disposal site/strategy. The recommended iodine fixation forms, based on their leach resistance and chemical stability and contingent on the disposal strategy/site and capture technique, are silver iodide in cement and barium, calcium, or strontium, and mercuric iodates in cement. Iodine sodalite appears promising and merits further study. If compatible with disposal requirements, the recommended forms for Mercurex and Iodox are insoluble iodates in cement and for silver sorbents the sorbents in cement or AgI in cement. Conversion between the different oxidation states of iodine is feasible but complicates the iodine treatment. For the different disposal strategies, isotopic dilution or ocean disposal has the least stringent disposal form requirements. Any of the recommended forms should be suitable with proper site selection. Isolation in a geologic repository for thousands of years requires the disposal form to be thermally and chemically stable and resistant to leaching at elevated temperatures. Probably the best form studied for isolation is silver iodide in cement. For extraterrestrial disposal, the disposal form may have to withstand reentry impact and surface disposal in the event of an aborted mission; this assumes the capsule is not recovered. Thus the primary containment barrier is critical. The suggested iodine form for space disposal is a heavy metal iodide.

Burger, L.L.; Scheele, R.D.; Wiemers, K.D.

1981-12-01T23:59:59.000Z

68

Deep Bed Iodine Sorbent Testing FY 2011 Report  

Science Conference Proceedings (OSTI)

Nuclear fission results in the production of fission products (FPs) and activation products that increasingly interfere with the fission process as their concentrations increase. Some of these fission and activation products tend to evolve in gaseous species during used nuclear fuel reprocessing. Analyses have shown that I129, due to its radioactivity, high potential mobility in the environment, and high longevity (half life of 15.7 million years), can require control efficiencies of up to 1,000x or higher to meet regulatory emission limits. Deep-bed iodine sorption testing has been done to evaluate the performance of solid sorbents for capturing iodine in off-gas streams from nuclear fuel reprocessing plants. The objectives of the FY 2011 deep bed iodine sorbent testing are: (1) Evaluate sorbents for iodine capture under various conditions of gas compositions and operating temperature (determine sorption efficiencies, capacities, and mass transfer zone depths); and (2) Generate data for dynamic iodine sorption modeling. Three tests performed this fiscal year on silver zeolite light phase (AgZ-LP) sorbent are reported here. Additional tests are still in progress and can be reported in a revision of this report or a future report. Testing was somewhat delayed and limited this year due to initial activities to address some questions of prior testing, and due to a period of maintenance for the on-line GC. Each test consisted of (a) flowing a synthetic blend of gases designed to be similar to an aqueous dissolver off-gas stream over the sorbent contained in three separate bed segments in series, (b) measuring each bed inlet and outlet gas concentrations of iodine and methyl iodide (the two surrogates of iodine gas species considered most representative of iodine species expected in dissolver off-gas), (c) operating for a long enough time to achieve breakthrough of the iodine species from at least one (preferably the first two) bed segments, and (d) post-test purging with pure N2 to drive loosely or physisorbed iodine species off of the sorbent. Post-test calculations determine the control efficiencies for each bed, iodine loadings on the sorbent, and mass transfer zone depths. Portions of the iodine-laden sorbent from the first bed of two of the tests have been shipped to SNL for waste form studies. Over the past three years, we have explored a full range of inlet iodine and methyl iodide concentrations ranging from {approx}100 ppb to {approx}100 ppm levels, and shown adequate control efficiencies within a bed depth as shallow as 2 inches for lower concentrations and 4 inches for higher concentrations, for the AgZ-type sorbents. We are now performing a limited number of tests in the NC-77 sorbent from SNL. Then we plan to continue to (a) fill in data gaps needed for isotherms and dynamic sorbent modeling, and (b) test the performance of additional sorbents under development.

Nick Soelberg; Tony Watson

2011-08-01T23:59:59.000Z

69

Low sintering temperature glass waste forms for sequestering radioactive iodine  

Science Conference Proceedings (OSTI)

Materials and methods of making low-sintering-temperature glass waste forms that sequester radioactive iodine in a strong and durable structure. First, the iodine is captured by an adsorbant, which forms an iodine-loaded material, e.g., AgI, AgI-zeolite, AgI-mordenite, Ag-silica aerogel, ZnI.sub.2, CuI, or Bi.sub.5O.sub.7I. Next, particles of the iodine-loaded material are mixed with powdered frits of low-sintering-temperature glasses (comprising various oxides of Si, B, Bi, Pb, and Zn), and then sintered at a relatively low temperature, ranging from 425.degree. C. to 550.degree. C. The sintering converts the mixed powders into a solid block of a glassy waste form, having low iodine leaching rates. The vitrified glassy waste form can contain as much as 60 wt % AgI. A preferred glass, having a sintering temperature of 500.degree. C. (below the silver iodide sublimation temperature of 500.degree. C.) was identified that contains oxides of boron, bismuth, and zinc, while containing essentially no lead or silicon.

Nenoff, Tina M.; Krumhansl, James L.; Garino, Terry J.; Ockwig, Nathan W.

2012-09-11T23:59:59.000Z

70

NIST{endash}JANAF Thermochemical Tables for the Iodine Oxides  

Science Conference Proceedings (OSTI)

The thermodynamic and spectroscopic properties of the iodine oxide species have been reviewed. Recommended NIST{endash}JANAF Thermochemical Tables are given for six gaseous iodine oxides: IO, OIO, IOO, IOI, IIO, and IO{sub 3}. Sufficient information is not available to generate thermochemical tables for any condensed phase species. Annotated bibliographies (over 400 references) are provided for all neutral iodine oxides which have been reported in the literature. There is a lack of experimental thermodynamic and spectroscopic information for all iodine oxide species, except IO(g) and OIO(g). The recommended thermochemical tables are based on estimates for the structure, vibrational frequencies, and enthalpy of formation based in part on the spectroscopic and thermodynamic data for the other halogen oxides [J. Phys. Chem. Ref. Data {bold 25}, 551 (1996); {bold 25}, 1061 (1996)]. Although there is a definite lack of information in comparison with the other halides, this information is provided for the iodine oxides for the following reasons: (1) to complete the study of the halogen oxide family and (2) to stress the need for additional experimental measurements. Of all the species mentioned in the literature, many have not been isolated or characterized. In fact, some do not exist. Throughout this paper, uncertainties attached to recommended values correspond to the uncertainty interval, equal to twice the standard deviation of the mean. {copyright} {ital 1996 American Institute of Physics and American Chemical Society.}

Chase, M.W. [Standard Reference Data Program, National Institute of Standards and Technology, Gaithersburg, Maryland 20879 (United States)

1996-09-01T23:59:59.000Z

71

1758 J. Phys. Chem. 1992, 96, 1758-1764 Ab Initio MO Study of the Thermal Decomposition of Fluorinated Disilanes,  

E-Print Network (OSTI)

of Fluorinated Disilanes, Edgar W. Ignaciot and H. Bernhard Schlegel* Department of Chemistry, Wayne State disilane, the SiH2+ SiH, and SiH3SiH+ H2paths are favored over other modes of decomposition Fluorinated silanes and disilanes, and reactive intermediates derived from these compounds, are important

Schlegel, H. Bernhard

72

High rate chemical vapor deposition of carbon films using fluorinated gases  

DOE Patents (OSTI)

A high rate, low temperature deposition of amorphous carbon films is produced by PE-CVD in the presence of a fluorinated or other halide gas. The deposition can be 5 performed at less than 100C, including ambient room temperature, with a radio frequency plasma assisted chemical vapor deposition process. With less than 6.5 at% fluorine incorporated into the amorphous carbon film, the characteristics of the carbon film, including index of 10 refraction, mass density, optical clarity, and chemical resistance are within 15% of those characteristics for pure amorphous carbon films, but the deposition rates are high.

Stafford, B.L.; Tracy, C.E.; Benson, D.K.; Nelson, A.J.

1991-03-15T23:59:59.000Z

73

High rate chemical vapor deposition of carbon films using fluorinated gases  

DOE Patents (OSTI)

A high rate, low-temperature deposition of amorphous carbon films is produced by PE-CVD in the presence of a fluorinated or other halide gas. The deposition can be performed at less than 100.degree. C., including ambient room temperature, with a radio frequency plasma assisted chemical vapor deposition process. With less than 6.5 atomic percent fluorine incorporated into the amorphous carbon film, the characteristics of the carbon film, including index of refraction, mass density, optical clarity, and chemical resistance are within fifteen percent (15%) of those characteristics for pure amorphous carbon films, but the deposition rates are high.

Stafford, Byron L. (Arvada, CO); Tracy, C. Edwin (Golden, CO); Benson, David K. (Golden, CO); Nelson, Arthur J. (Longmont, CO)

1993-01-01T23:59:59.000Z

74

Light-Induced Passivation of Si by Iodine Ethanol Solution: Preprint  

DOE Green Energy (OSTI)

We report on our observations of light-activated passivation of silicon surfaces by iodine-ethanol solution.

Sopori, B.; Rupnowski, P.; Appel, J.; Guhaabiswas, D.; Anderson-Jackson, L.

2009-02-01T23:59:59.000Z

75

Method for selectively removing fluorine and fluorine-containing contaminants from gaseous UF/sub 6/. [ClF/sub 3/  

DOE Patents (OSTI)

This invention is a method for effecting preferential removal and immobilization of certain gaseous contaminants from gaseous UF/sub 6/. The contaminants include fluorine and fluorides which are more reactive with CaCO/sub 3/ than is UF/sub 6/. The method comprises contacting the contaminant-carrying UF/sub 6/ with particulate CaCO/sub 3/ at a temperature effecting reaction of the contaminant and the CaCO/sub 3/.

Jones, R.L.; Otey, M.G.; Perkins, R.W.

1980-11-24T23:59:59.000Z

76

Study of surface fluorination of photocatalytic TiO{sub 2} by thermal shock method  

Science Conference Proceedings (OSTI)

Surface fluorinated TiO{sub 2} powders were prepared by thermal shock method and an overall comparative study was achieved on the basis of XRD, SEM, UV-vis and XPS analyses. The main objective was to elucidate the influences of surface fluorination on the crystallite structures, morphologies, optical properties and surface chemistry with the temperature. According to the results, the surface fluorination under thermal shock method below 600 Degree-Sign C did not change the crystallite structure and the particles size, but successfully created chemisorbed fluoride ions, oxygen vacancies and increased the hydroxyl groups on the surface of TiO{sub 2}. The presence of oxygen vacancies was assigned to the red shift of TiO{sub 2} optical absorption edge, which was the origin of visible-light-induced photocatalytic activity of these samples. For the thermal shock temperatures over 600 Degree-Sign C, the K{sub 2}Ti{sub 6}O{sub 13}-like phase was formed, resulting from the decrease of surface hydroxyl groups and the blue shift in absorption edge which reduced the photocatalytic activity. - Graphical abstract: The influence of fluorination on the surface of TiO{sub 2} by thermal shock method at several temperatures has been investigated by following the evolution of the F1s spectra obtained by X-ray photoelectron spectroscopy. The blank peaks are assigned to the chemisorbed fluoride ions on the samples surface and the filled peaks to fluorine atoms in oxygenated environment of solid solution TiO{sub 2-x}F{sub x}, which is originated from the substitution of F ions for O ions in the TiO{sub 2} lattice. Highlights: Black-Right-Pointing-Pointer Surface fluorination of TiO{sub 2} P25 by thermal shock method. Black-Right-Pointing-Pointer Structure, morphology, surface and photocatalytic properties of fluorinated TiO{sub 2}. Black-Right-Pointing-Pointer Low thermal shock temperatures increase the photocatalytic activity. Black-Right-Pointing-Pointer Fluoride ions chemisorbed on the surface without structure and morphology change. Black-Right-Pointing-Pointer Formation of K{sub 2}Ti{sub 6}O{sub 13} phase at high thermal shock temperatures.

Tien Khoa Le [IPREM/ECP (UMR 5254), University of Pau, Helioparc, 2 av. Pierre Angot, 64053 Pau cedex 9 (France); University of Science - Ho Chi Minh city, 227 Nguyen Van Cu Street, Ho Chi Minh City (Viet Nam); Flahaut, Delphine, E-mail: delphine.flahaut@univ-pau.fr [IPREM/ECP (UMR 5254), University of Pau, Helioparc, 2 av. Pierre Angot, 64053 Pau cedex 9 (France); Foix, Dominique; Blanc, Sylvie [IPREM/ECP (UMR 5254), University of Pau, Helioparc, 2 av. Pierre Angot, 64053 Pau cedex 9 (France); Huu Khanh Hung Nguyen; Thi Kieu Xuan Huynh [University of Science - Ho Chi Minh city, 227 Nguyen Van Cu Street, Ho Chi Minh City (Viet Nam); Martinez, Herve [IPREM/ECP (UMR 5254), University of Pau, Helioparc, 2 av. Pierre Angot, 64053 Pau cedex 9 (France)

2012-03-15T23:59:59.000Z

77

Evaporation of iodine-containing off-gas scrubber solution  

DOE Patents (OSTI)

Mercuric nitrate-nitric acid scrub solutions containing radioiodine may be reduced in volume without excessive loss of volatile iodine. The use of concentrated nitric acid during an evaporation process oxidizes the mercury-iodide complex to a less volatile mercuric iodate precipitate.

Partridge, J.A.; Bosuego, G.P.

1980-07-14T23:59:59.000Z

78

Labeling of indocyanine green with carrier-free iodine-123  

DOE Patents (OSTI)

The method of labeling indocyanine green (ICG) with carrier-free iodine-123 comprising the steps of condensing xenon-123 on crystals of ICG followed by permitting decay of the .sup.123 Xe a sufficient length of time to produce .sup.123 I-electronically excited ions and atoms which subsequently label ICG.

Ansari, Azizullah N. (Mount Sinai, NY); Lambrecht, Richard M. (East Quogue, NY); Redvanly, Carol S. (Upton, NY); Wolf, Alfred P. (East Setauket, NY)

1976-01-01T23:59:59.000Z

79

Downstream Behavior of Volatile Iodine, Cesium, and Tellurium Fission Products  

Science Conference Proceedings (OSTI)

A better understanding of how iodine, cesium, and tellurium fission products deposit on primary reactor components during a degraded core accident can help utility analysts improve computer codes that model product behavior. The mathematical model developed in this study predicts the behavior of deposited products vaporized or revaporized by self-heating in a reactor accident.

1989-01-17T23:59:59.000Z

80

CORROSION ASSOCIATED WITH FLUORINATION IN THE OAK RIDGE NATIONAL LABORATORY FLUORIDE VOLATILITY PROCESS  

SciTech Connect

: : 9 7 7 8 6 9 : = 7 9 9used during the fluorination of fused-salt fuels and subsequent associated operations in the Oak Ridge National Laboratory (ORNL) Fluoride Volatility Process was evaluated. Corrosive attack is reported as mils per month based on molten salt residence time or mils per hour based on fluorine exposure time. Two fluorinators were used in the VPP to carry out the fluorination reactions. These vessels, Mark I and Mark II, were fabricated into right cylinders, approx 4 1/2 ft in height, from the same heat of L (low carbon nickel. The first vessel contained equimolar NaF- ZrF/sub 4/ or NaF-ZrF/sub 4/-UF/sub 4/ (48-48-4 mole%) for approx 1250 hr at 600 to 725 deg C. Over a period of 61 hr, 57,500 standard liters of F/sub 2/ were sparged into the slats. This constituted a F/sub 2/:U mole ratio of 3:1 beyond theoretical requirements. The Mark II fluorinator contained fluoride salts of approxi-mately the same compositions plus small additions of PuF/sub 4/ during three runs. The salts were kept molten at 540 to 730 deg C for approx 1950 hr and about sixty 500 standard liters of F/sub 2/ were sparged into the Mark II melts in 92 hr. Both fluorinators sustained large corrosion losses consisting of extensive wall thinning, severe interior inter- granular attack, and a moderate exterior oxidation attack. Maximum deterioration on the Mark I vessel occurred in the middle vapor region at a calculated rate of 1.2 mils/hr, based on fluorine sparge time, or 46 mils/month, based on time of exposure to molten salts. The second vessel showed maximum attack in the salt-containing region at similarly calculated rates of 1.1 mils/hr and 60 mils/month. Some evidence was found to indicate that the intergranular attack may have resulted from sulfur in the systems. Bulk metal losses from the vessel's walls were believed to be the result of cyclic losses of NiF/sub 2/ ""protective'' films. The shift in maximum corrosion attack geometry in the two fluorinators is believed to have resulted from differences in operating conditions. The Mark II vessel experienced higher temperatures, longer fluorine exposure times, and uranium residence times in its salt baths. Specimens removed from the wall of the first fluorinator showed a variation in aversge ASTM grain-size number of 5 or 6 to >1, the largest grains being found in the middle vapor region. The second vessel had a more uniform grain-size pattern, average ASTM grain-size numbers varying from 3 to 5 to 2 to 4. The variations in grain sizes are believed to have resulted from variable heating rates during initial usage. Examinations of bench-scale reactors, where simulated fluorination environments were provided to study process variables and corrosion, showed that A nickel had the highest degree of corrosion resistance as a fluorinator materiai of construction when compared with Inconel and INOR-8. Intergranular penetration and subsequent sloughing of whole grains seemed to be the predominant mode of corrosive attack on the Inconel vessel. At the higher test temperatures, 600 deg C, INOR-8 miniature fluorinators showed large bulk metal losses plus selective losses of chromium, molybdenum, and iron from the exposed alloy surfaces. Evidence of a marked reduction in attack on nickel and INOR-8 was found during lower temperature studies at 450 to 525 deg C. Scouting corrosion tests were performed in the VPP's fluorinators using rod, sheet, or wire specimens of commercial and developmental alloys. These tests were subjected to serious limitations due to the lack of control over operating conditions and thus considerable variation in the corrosion of L nickel control specimens resulted. Those nickel-rich alloys containing iron and cobalt showed some superiority in corrosion resistsnce when com- pared with L nickel specimens. Nickel-rich alloys containing molybdenum additions showed variable behavior in the fluorination environment. Additional experimental nickelbase alloy corrosion specimens, containing magnesium,

Litman, A.P.; Goldman, A.E.

1961-06-19T23:59:59.000Z

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


81

Silicon structuring by etching with liquid chlorine and fluorine precursors using femtosecond laser pulses  

SciTech Connect

The aim of this study is to investigate the micrometer and submicrometer scale structuring of silicon by liquid chlorine and fluorine precursors with 200 fs laser pulses working at both fundamental (775 nm) and frequency doubled (387 nm) wavelengths. The silicon surface was irradiated at normal incidence by immersing the Si (111) substrates in a glass container filled with liquid chlorine (CCl{sub 4}) and fluorine (C{sub 2}Cl{sub 3}F{sub 3}) precursors. We report that silicon surfaces develop an array of spikes with single step irradiation processes at 775 nm and equally at 387 nm. When irradiating the Si surface with 400 pulses at 330 mJ/cm{sup 2} laser fluence and a 775 nm wavelength, the average height of the formed Si spikes in the case of fluorine precursors is 4.2 {mu}m, with a full width at half maximum of 890 nm. At the same irradiation wavelength chlorine precursors develop Si spikes 4 {mu}m in height and with a full width at half maximum of 2.3 {mu}m with irradiation of 700 pulses at 560 mJ/cm{sup 2} laser fluence. Well ordered areas of submicrometer spikes with an average height of about 500 nm and a width of 300 nm have been created by irradiation at 387 nm by chlorine precursors, whereas the fluorine precursors fabricate spikes with an average height of 700 nm and a width of about 200 nm. Atomic force microscopy and scanning electron microscopy of the surface show that the formation of the micrometer and sub-micrometer spikes involves a combination of capillary waves on the molten silicon surface and laser-induced etching of silicon, at both 775 nm and 387 nm wavelength irradiation. The energy-dispersive x-ray measurements indicate the presence of chlorine and fluorine precursors on the structured surface. The fluorine precursors create a more ordered area of Si spikes at both micrometer and sub-micrometer scales. The potential use of patterned Si substrates with gradient topography as model scaffolds for the systematic exploration of the role of 3D micro/nano morphology on cell adhesion and growth is envisaged.

Radu, C.; Simion, S.; Zamfirescu, M.; Ulmeanu, M. [Laser Department, National Institute for Laser, Plasma and Radiation Physics, Atomistilor Str. 409, P.O. Box MG-36, 077125 Magurele-Bucharest (Romania); Enculescu, M. [National Institute of Material Physics, Atomistilor Str. 105 bis, P.O. Box MG-7, 077125 Magurele-Bucharest (Romania); Radoiu, M. [SAIREM SAS, 12 porte du Grand Lyon, P.O. Box 80214, 01700 Neyron (France)

2011-08-01T23:59:59.000Z

82

Low-Temperature Fluorination of Soft-Templated Mesoporous Carbons for a High-Power Lithium/Carbon Fluoride Battery  

Science Conference Proceedings (OSTI)

Soft-templated mesoporous carbons and activated mesoporous carbons were fluorinated using elemental fluorine between room temperature and 235 C. The mesoporous carbons were prepared via self-assembly synthesis of phloroglucinol formaldehyde as a carbon precursor in the presence of triblock ethylene oxide propylene oxide ethylene oxide copolymer BASF Pluronic F127 as the template. The F/C ratios ranged from 0.15 to 0.75 according to gravimetric, energy dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy analysis. Materials have mesopore diameters up to 11 nm and specific surface areas as high as 850 m2 g 1 after fluorination as calculated from nitrogen adsorption isotherms at 196 C. Furthermore, the materials exhibit higher discharge potentials and energy and power densities as well as faster reaction kinetics under high current densities than commercial carbon fluorides with similar fluorine contents when tested as cathodes for Li/CFx batteries.

Fulvio, Pasquale F [ORNL; Dai, Sheng [ORNL; Guo, Bingkun [ORNL; Mahurin, Shannon Mark [ORNL; Mayes, Richard T [ORNL; Sun, Xiao-Guang [ORNL; Veith, Gabriel M [ORNL; Brown, Suree [ORNL; Adcock, Jamie [University of Tennessee, Knoxville (UTK)

2011-01-01T23:59:59.000Z

83

Hanging coverslip method for cell surface iodination of monolayer cultures  

SciTech Connect

A procedure is described by which the use of a 1,3,4,6-tetrachloro-3 alpha,6 alpha-diphenyl glycoluril (iodogen)-coated coverslip to iodinate the cell surface proteins of monolayer cultures has been improved by hanging the coverslip at a defined distance from the cells. This method allows gentle manipulation of the cell culture, resulting in retention of high cell viability and in recovery of the cell monolayer with a minimum of mechanical damage. In addition, it allows the safe disposal of the radioactive coverslip upon completion of the reaction. Finally, the labeling is surface specific. The application of this procedure to 3T3 fibroblasts results in labeling of proteins comparable to lactoperoxidase-catalyzed iodinations.

Moutsatsos, I.K.; Cok, S.J.

1985-08-01T23:59:59.000Z

84

Polymer electrolyte membranes from fluorinated polyisoprene-block-sulfonated polystyrene: Structural evolution with hydration and heating  

Science Conference Proceedings (OSTI)

Small-angle neutron scattering (SANS) and ultra-small-angle X-ray scattering (USAXS) have been used to study the structural changes in fluorinated polyisoprene/sulfonated polystyrene (FISS) diblock copolymers as they evolved from the dry state to the water swollen state. A dilation of the nanometer-scale hydrophilic domains has been observed as hydration increased, with greater dilation occurring in the more highly sulfonated samples or upon hydration at higher temperatures. Furthermore, a decrease in the order in these phase separated structures is observed upon swelling. The glass transition temperatures of the fluorinated blocks have been observed to decrease upon hydration of these materials, and at the highest hydration levels, differential scanning calorimetry (DSC) has shown the presence of tightly bound water. A precipitous drop in the mechanical integrity of the 50% sulfonated materials is also observed upon exceeding the glass transition temperature (Tg), as measured by dynamic mechanical analysis (DMA).

Sodeye, Akinbode [Department of Polymer Science and Engineering, University of Massachusetts; Huang, Tianzi [University of Tennessee, Knoxville (UTK); Gido, Samuel [University of Massachusetts, Amherst; Mays, Jimmy [ORNL

2011-01-01T23:59:59.000Z

85

Synthesis of carbon-11, fluorine-18, and nitrogen-13 labeled radiotracers for biomedical applications  

SciTech Connect

A number of reviews, many of them recent, have appeared on various aspects of /sup 11/C, /sup 18/F and /sup 13/N-labeled radiotracers. This monograph treats the topic principally from the standpoint of synthetic organic chemistry while keeping in perspective the necessity of integrating the organic chemistry with the design and ultimate application of the radiotracer. Where possible, recent examples from the literature of organic synthesis are introduced to suggest potentially new routes which may be applied to problems in labeling organic molecules with the short-lived positron emitters, carbon-11, fluorine-18, and nitrogen-13. The literature survey of carbon-11, fluorine-18 and nitrogen-13 labeled compounds presented are of particular value to scientists working in this field. Two appendices are also included to provide supplementary general references. A subject index concludes this volume.

Fowler, J.S.; Wolf, A.P.

1981-01-01T23:59:59.000Z

86

Benzo(C)fluorine, PAH with possible human health implications. (To BAP or  

NLE Websites -- All DOE Office Websites (Extended Search)

Benzo(C)fluorine, PAH with possible human health implications. (To BAP or Benzo(C)fluorine, PAH with possible human health implications. (To BAP or not to BAP) Speaker(s): Larry Goldstein Date: November 7, 2000 - 12:00pm Location: 90-3122 Polycyclic aromatic hydrocarbons (PAH) are ubiquitous environmental contaminants with potential health consequences. Essentially all the cancer risk from exposure to coal tar, cigarette smoke and other products of incomplete combustion is thought to reflect the contributions of PAHs with 4 or more fused rings. In risk assessment as currently practiced the major contributor to overall risk is the 5-ring PAH benzo(a)pyrene (B(a)P).However, recent studies using a lifetime feeding protocol indicate that B(a)P does not meet criteria for application to risk assessment since it does not induce lung tumors, the endpoint upon which risk assessments

87

Some Investigations of the Reaction of Activated Charcoal with Fluorine and Uranium Hexafluoride  

SciTech Connect

The Molten Salt Reactor Experiment (MSRE) at Oak Ridge National Laboratory has been shut down since 1969, when the fuel salt was drained from the core into two Hastelloy N drain tanks at the reactor site. Over time, fluorine (F{sub 2}) and uranium hexafluoride (UF{sub 6}) moved from the salt through the gas piping to a charcoal bed, where they reacted with the activated charcoal. Some of the immediate concerns related to the migration of F{sub 2} and UF{sub 6} to the charcoal bed were the possibility of explosive reactions between the charcoal and F{sub 2}, the existence of conditions that could induce a criticality accident, and the removal and recovery of the fissile uranium from the charcoal. This report addresses the reactions and reactivity of species produced by the reaction of fluorine and activated charcoal and between charcoal and F{sub 2}-UF{sub 6} gas mixtures in order to support remediation of the MSRE auxiliary charcoal bed (ACB) and the recovery of the fissile uranium. The chemical identity, stoichiometry, thermochemistry, and potential for explosive decomposition of the primary reaction product, fluorinated charcoal, was determined.

Del Cul, G.D.; Fiedor, J.N.; Simmons, D.W.; Toth, L.M.; Trowbridge, L.D.; Williams

1998-09-01T23:59:59.000Z

88

Transition of Iodine Analysis to Accelerator Mass Spectrometry  

SciTech Connect

Funding was received from NA-22 to investigate transitioning iodine isotopic analyses to an accelerator mass spectrometry (AMS) system. The present method uses gas-phase chemistry followed by thermal ionization mass spectrometry (TIMS). It was anticipated that the AMS approach could provide comparable data, with improved background levels and superior sample throughput. An aqueous extraction method was developed for removal of iodine species from high-volume air filters. Ethanol and sodium hydroxide, plus heating and ultrasonic treatment, were used to successfully extract iodine from loaded high-volume air filters. Portions of the same filters were also processed in the traditional method and analyzed by TIMS for comparison. Aliquot parts of the aqueous extracts were analyzed by AMS at the Swiss Federal Institute of Technology. Idaho National Laboratory (INL) personnel visited several AMS laboratories in the US, Spain, and Switzerland. Experience with AMS systems from several manufacturers was gained, and relationships were developed with key personnel at the laboratories. Three batches of samples were analyzed in Switzerland, and one in Spain. Results show that the INL extraction method successfully extracted enough iodine from high-volume air filters to allow AMS analysis. Comparison of the AMS and TIMS data is very encouraging; while the TIMS showed about forty percent more atoms of 129I, the 129/127 ratios tracked each other very well between the two methods. The time required for analysis is greatly reduced for the aqueous extraction/AMS approach. For a hypothetical batch of thirty samples, the AMS methodology is about five times faster than the traditional gas-phase chemistry and TIMS analysis. As an additional benefit, background levels for the AMS method are about 1000 times lower than for TIMS. This results from the fundamental mechanisms of ionization in the AMS system and cleanup of molecular interferences. We showed that an aqueous extraction of high-volume air filters, followed by isotopic analysis by AMS, can be used successfully to make iodine measurements with results comparable to those obtained by filter combustion and TIMS analysis.

J. E. Delmore

2010-09-01T23:59:59.000Z

89

On the Use of Thermal NF3 as the Fluorination and Oxidation Agent in Treatment of Used Nuclear Fuels  

SciTech Connect

This paper presents results of our investigation on the use of nitrogen trifluoride as the fluorination or fluorination/oxidation agent for use in a process for separating valuable constituents from used nuclear fuels by employing the volatility of many transition metal and actinide fluorides. Nitrogen trifluoride is less chemically and reactively hazardous than the hazardous and aggressive fluorinating agents used to prepare uranium hexafluoride and considered for fluoride volatility based nuclear fuels reprocessing. In addition, nitrogen trifluoride’s less aggressive character may be used to separate the volatile fluorides from used fuel and from themselves based on the fluorination reaction’s temperature sensitivity (thermal tunability) rather than relying on differences in sublimation/boiling temperature and sorbents. Our thermodynamic calculations found that nitrogen trifluoride has the potential to produce volatile fission product and actinide fluorides from candidate oxides and metals. Our simultaneous thermogravimetric and differential thermal analyses found that the oxides of lanthanum, cerium, rhodium, and plutonium fluorinated but did not form volatile fluorides and that depending on temperature volatile fluorides formed from the oxides of niobium, molybdenum, ruthenium, tellurium, uranium, and neptunium. We also demonstrated near-quantitative removal of uranium from plutonium in a mixed oxide.

Scheele, Randall D.; McNamara, Bruce K.; Casella, Andrew M.; Kozelisky, Anne E.

2012-05-01T23:59:59.000Z

90

Storage of LWR spent fuel in air. Volume 3, Results from exposure of spent fuel to fluorine-contaminated air  

SciTech Connect

The Behavior of Spent Fuel in Storage (BSFS) Project has conducted research to develop data on spent nuclear fuel (irradiated U0{sub 2}) that could be used to support design, licensing, and operation of dry storage installations. Test Series B conducted by the BSFS Project was designed as a long-term study of the oxidation of spent fuel exposed to air. It was discovered after the exposures were completed in September 1990 that the test specimens had been exposed to an atmosphere of bottled air contaminated with an unknown quantity of fluorine. This exposure resulted in the test specimens reacting with both the oxygen and the fluorine in the oven atmospheres. The apparent source of the fluorine was gamma radiation-induced chemical decomposition of the fluoro-elastomer gaskets used to seal the oven doors. This chemical decomposition apparently released hydrofluoric acid (HF) vapor into the oven atmospheres. Because the Test Series B specimens were exposed to a fluorine-contaminated oven atmosphere and reacted with the fluorine, it is recommended that the Test Series B data not be used to develop time-temperature limits for exposure of spent nuclear fuel to air. This report has been prepared to document Test Series B and present the collected data and observations.

Cunningham, M.E.; Thomas, L.E.

1995-06-01T23:59:59.000Z

91

Iodine photodissociation laser with an intracavity space - time light modulator  

SciTech Connect

A scheme of an iodine laser with two different intracavity space - time modulators based on electrooptic PLZT ceramics is experimentally studied. It is shown that lasing can occur in different angular directions with the use of both modulators. The output laser energy is 10 mJ with a pulse duration of 200 {mu}s and a beam divergence of 6.3 Multiplication-Sign 10{sup -4} rad. The laser field of view (5.1 Multiplication-Sign 10{sup -3} rad) consists of a discrete set of 8 Multiplication-Sign 8 directions. (control of laser radiation parameters)

Kachalin, G N; Pevny, S N; Pivkin, A N; Safronov, A S [Russian Federal Nuclear Center 'All-Russian Research Institute of Experimental Physics', Sarov, Nizhnii Novgorod region (Russian Federation)

2012-08-31T23:59:59.000Z

92

Physicochemical characterization of point defects in fluorine doped tin oxide films  

SciTech Connect

The physical and chemical properties of spray deposited FTO films are studied using FESEM, x-ray diffraction (XRD), x-ray photoelectron spectroscopy (XPS), electrical and optical measurements. The results of XRD measurements showed that the films are polycrystalline (grain size 20-50 nm) with Rutile structure and mixed preferred orientation along the (200) and (110) planes. An angular shift of the XRD peaks after F-doping is observed and interpreted as being due to the formation of substitutional fluorine defects (F{sub O}) in presence of high concentration of oxygen vacancies (V{sub O}) that are electrically neutral. The electrical neutrality of oxygen vacancies is supported by the observation that the electron concentration n is two orders of magnitude lower than the V{sub O} concentration calculated from chemical analyses using XPS measurements. It is shown that an agreement between XPS, XRD, and Hall effect results is possible provided that the degree of deviation from stoichiometry is calculated with the assumption that the major part of the bulk carbon content is involved in O-C bonds. High temperature thermal annealing is found to cause an increase in the F{sub O} concentration and a decrease in both n and V{sub O} concentrations with the increase of the annealing temperature. These results could be interpreted in terms of a high temperature chemical exchange reaction between the SnO{sub 2} matrix and a precipitated fluoride phase. In this reaction, fluorine is released to the matrix and Sn is trapped by the fluoride phase, thus creating substitutional fluorine F{sub O} and tin vacancy V{sub Sn} defects. The enthalpy of this reaction is determined to be approximately 2.4 eV while the energy of formation of a V{sub Sn} through the migration of Sn{sub Sn} host atom to the fluoride phase is approximately 0.45 eV.

El Akkad, Fikry; Joseph, Sudeep [Physics Department, Kuwait University, P.O. Box 5969, Safat 13060 (Kuwait)

2012-07-15T23:59:59.000Z

93

UF/sub 6//sup -/ production from surface reactions of uranium and fluorine  

SciTech Connect

The production of UF/sub 6//sup -/ by reaction of a collimated stream of fluorine gas with a resistively heated uranium wire was studied at temperatures from 870 to 1020/sup 0/C and pressures less than 10/sup -3/ torr. At these temperatures below the uranium melting point, the formation of UF/sub 3/ intermediate on the uranium surface resulted in low UF/sub 6//sup -/ yields. The kinetic energy of the UF/sub 6//sup -/ ion was on the order of thermal energies. The work function of uranium was measured to be 4.20 +- 0.14 eV.

McLean, J.E.; Dillon, J.J.; Talbert, C.M.

1978-10-19T23:59:59.000Z

94

Materials for high-temperature hydrogen fluorine environments. Final report, June 1976-December 1978  

DOE Green Energy (OSTI)

A determination has been made of the stability of 35 materials under high-temperature, fluorine rich, hydrogen fluoride torch testing. Refractory materials tested included 4 borides, 3 carbides, 3 nitrides, 12 oxides, 1 oxynitride, 1 sulfide, 10 metals, and carbon (10 types). Three materials distinctly performed better than nickel: lanthanum hexaboride, calcium hexaboride, and lanthanum silicon oxynitride. Of these, lanthanum hexaboride is the best candidate tested since it has an estimated upper use temperature > 1726 K, which is above the melting point and more than 300 K above the upper use temperature of nickel.

Holcombe, C.E. Jr.; Kovach, L.

1981-03-01T23:59:59.000Z

95

Improved efficiency in the sulfur dioxide-iodine hydrogen cycle through the use of magnesium oxide  

DOE Green Energy (OSTI)

The reaction of iodine with dry magnesium oxide and magnesium sulfite hexahydrate was studied experimentally as a possible means of improving the efficiency of the sulfur dioxide-iodine cycle. When no extra water was introduced, the maximum product yield was 67% obtained at 423 K. With excess water vapor, a nonporous plug was formed which prevented complete reaction. In the second case, maximum yield was 62% measured at 433 K showing that added water does not increase reaction products. This reaction gives an alternate route for producing hydrogen from water via the sulfur dioxide-iodine process.

Mason, C.F.V.; Bowman, M.G.

1981-01-01T23:59:59.000Z

96

ALTERNATIVE FLOWSHEETS FOR THE SULFUR-IODINE THERMOCHEMICAL HYDROGEN CYCLE  

DOE Green Energy (OSTI)

OAK-B135 A hydrogen economy will need significant new sources of hydrogen. Unless large-scale carbon sequestration can be economically implemented, use of hydrogen reduces greenhouse gases only if the hydrogen is produced with non-fossil energy sources. Nuclear energy is one of the limited options available. One of the promising approaches to produce large quantities of hydrogen from nuclear energy efficiently is the Sulfur-Iodine (S-I) thermochemical water-splitting cycle, driven by high temperature heat from a helium Gas-Cooled Reactor. They have completed a study of nuclear-driven thermochemical water-splitting processes. The final task of this study was the development of a flowsheet for a prototype S-I production plant. An important element of this effort was the evaluation of alternative flowsheets and selection of the reference design.

BROWN,LC; LENTSCH,RD; BESENBRUCH,GE; SCHULTZ,KR; FUNK,JE

2003-02-01T23:59:59.000Z

97

Hydrothermal synthesis of Sb2S3nanorods using iodine via redox mechanism  

Science Conference Proceedings (OSTI)

Crystalline antimony sulfide (Sb2S3) with nanorods morphology was successfully prepared via hydrothermal method by the reaction of elemental sulfur, antimony, and iodine as starting materials with high yield at 180°C for 24 ...

Abdolali Alemi; Sang Woo Joo; Younes Hanifehpour; Aliakbar Khandar; Ali Morsali; Bong-Ki Min

2011-01-01T23:59:59.000Z

98

Sorption and transport of iodine species in sediments from the Savannah River and Hanford Sites  

E-Print Network (OSTI)

Sorption and transport of iodine species in sediments from the Savannah River and Hanford Sites-iodoaniline) in sediments collected at the Savannah River and Hanford Sites, where anthropogenic 129 I from

Hu, Qinhong "Max"

99

Iodine and NO sub x behavior in the dissolver off-gas and IODOX (Iodine Oxidation) systems in the Oak Ridge National Laboratory Integrated Equipment Test facility  

SciTech Connect

This paper describes the most recent in a series of experiments evaluating the behavior of iodine and NO{sub x} in the Integrated Equipment Test (IET) Dissolver Off-Gas (DOG) System. This work was performed as part of a joint collaborative program between the US Department of Energy and the Power and Nuclear Fuel Development Corporation of Japan. The DOG system consists of two shell-and-tube heat exchangers in which water and nitric acid are removed from the dissolver off-gas by condensation, followed by a packed tower in which NO{sub x} is removed by absorption into a dilute nitric acid solution. The paper also describes the results of the operation of the Iodine Oxidation (IODOX) System. This system serves to remove iodine from the DOG system effluent by absorption into hyperazeotropic nitric acid. 7 refs., 11 figs., 10 tabs.

Birdwell, J.F.

1990-01-01T23:59:59.000Z

100

Laboratory weathering and solubility relationships of fluorine and molybdenum in combusted oil shale  

SciTech Connect

Proper management of large volumes of spent oil shale requires an understanding of the mineralogy and the disposal environment chemistry. Simulated laboratory weathering is one method to rapidly and inexpensively assess the long-term potential for spent oil shales to degrade the environment. The objectives of this study were to assess the solubility relationships of fluorine (F) and molybdenum (Mo) in Green River Formation spent oil shale, to examine the mineralogy and leachate chemistry of three combusted oil shales in a laboratory weathering environment using the humidity cell technique, and to examine the data from spent oil shale literature. Combusted oil shales from the Green River Formation and New Albany Shale were used in the examination of the leachate chemistry and mineralogy.

Essington, M.E.; Wills, R.A.; Brown, M.A.

1991-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


101

RADIOACTIVE IODINE IN THE LYMPH LEAVING THE THYROID GLAND  

SciTech Connect

Very high levels of I/sup 131/ were found in lymph of vessels draining the thyroid gland of animals injected with the isotope. The lymph was collected from the draining lymphatics 2-6 days after subcutaneous injection of 50-100 mu C in rabbits and cats and 200 mu C in sheep. Thyroid lymph contained a concentration of radioactivity considerably higher than that in either thyroid venous plasma or systemic blood plasma. This was found in all three species both before and after giving thyroid-stimulating hormone (TSH). Almost all the radioactivity in the lymph was due to organic I/sup 131/. When tie thyroid gland was excised postmortem, a count showed that the proportion of I/sup 131/ which had been injected and which rernained in the gland at the end of the experiment varied considerably. Estimates of the radiation dose varied between 30 and 200 rad. There was no obvious relation between this dose the lymph/plasma I/sup 131/ ratio, which indicates that the radiation dose was not so high as to produce damage to the gland. The radiation dose to the thyroid in these experiments was not greater than is customarily given in studies of hormone release from the thyroid and the dosage used gives a lower level of radiation than that thought to cause radiation damage to the gland. Since, therefore, damage to the thyroid can be discounted as a cause for the release of iodinated protein, it seems likely that a significart proportion of organic iodine leaves the gland under normal conditions via the lymphatic pathway both before and after the administration of TSH and that this pathway should be taken into account in all studies of thyroid secretion. Gentle massage of the gland, which increases the flow of lymph, did not lead to an increase in the output of radioactivity. Movement of lymph in the thyroid vessels is relatively rapid and since the concentration of I/sup 131/ in thyroid lymph is high, the amount of thyroid hormones leaving the gland by this pathway must be considerable. (BBB)

Daniel, R.M.; Gale, M.M.; Pratt, O.E.

1963-04-01T23:59:59.000Z

102

Nuclear Hydrogen Initiative, Results of the Phase II Testing of Sulfur-Iodine Integrated Lab Scale Experiments  

DOE Green Energy (OSTI)

International collaborative effort to construct a laboratory-scale Sulfur-Iodine process capable of producing 100-200 L/hr of hydrogen.

Benjamin Russ; G. Naranjo; R. Moore; W. Sweet; M. Hele; N. Pons

2009-10-30T23:59:59.000Z

103

Soil Iodine Determination in Deccan Syneclise, India: Implications for Near Surface Geochemical Hydrocarbon Prospecting  

Science Conference Proceedings (OSTI)

The association of iodine with organic matter in sedimentary basins is well documented. High iodine concentration in soils overlying oil and gas fields and areas with hydrocarbon microseepage has been observed and used as a geochemical exploratory tool for hydrocarbons in a few studies. In this study, we measure iodine concentration in soil samples collected from parts of Deccan Syneclise in the west central India to investigate its potential application as a geochemical indicator for hydrocarbons. The Deccan Syneclise consists of rifted depositional sites with Gondwana-Mesozoic sediments up to 3.5 km concealed under the Deccan Traps and is considered prospective for hydrocarbons. The concentration of iodine in soil samples is determined using ICP-MS and the values range between 1.1 and 19.3 ppm. High iodine values are characteristic of the northern part of the sampled region. The total organic carbon (TOC) content of the soil samples range between 0.1 and 1.3%. The TOC correlates poorly with the soil iodine (r{sup 2} propane-oxidizing bacterial populations in the soil. The integration of geochemical observations show the occurrence of elevated values in the northern part of the study area, which is also coincident with the presence of exposed dyke swarms that probably serve as conduits for hydrocarbon microseepage. The corroboration of iodine with existing geological, geophysical, and geochemical data suggests its efficacy as one of the potential tool in surface geochemical exploration of hydrocarbons. Our study supports Deccan Syneclise to be promising in terms of its hydrocarbon prospects.

Mani, Devleena, E-mail: devleenatiwari@ngri.res.in [National Geophysical Research Institute (Council of Scientific and Industrial Research) (India); Kumar, T. Satish [Oil India Limited (India); Rasheed, M. A.; Patil, D. J.; Dayal, A. M.; Rao, T. Gnaneshwar; Balaram, V. [National Geophysical Research Institute (Council of Scientific and Industrial Research) (India)

2011-03-15T23:59:59.000Z

104

FUNCTIONALIZED SILICA AEROGELS: ADVANCED MATERIALS TO CAPTURE AND IMMOBILIZE RADIOACTIVE IODINE  

Science Conference Proceedings (OSTI)

To support the future expansion of nuclear energy, an effective method is needed to capture and safely store radiological iodine-129 released during reprocessing of spent nuclear fuel. Various materials have been investigated to capture and immobilize iodine. In most cases, however, the materials that are effective for capturing iodine cannot subsequently be sintered/densified to create a stable composite that could be a viable waste form. We have developed chemically modified, highly porous, silica aerogels that show sorption capacities higher than 440 mg of I2 per gram at 150 C. An iodine uptake test in dry air containing 4.2 ppm of iodine demonstrated no breakthrough after 3.5 h and indicated a decontamination factor in excess of 310. Preliminary densification tests showed that the I2-loaded aerogels retained more than 92 wt% of I2 after thermal sintering with pressure assistance at 1200 C for 30 min. These high capture and retention efficiencies for I2 can be further improved by optimizing the functionalization process and the chemistry as well as the sintering conditions.

Matyas, Josef; Fryxell, Glen E.; Busche, Brad J.; Wallace, Krys; Fifield, Leonard S.

2011-11-16T23:59:59.000Z

105

Thermal-hydraulic response and iodine transport during a steam generator tube rupture  

SciTech Connect

Recent reanalyses of the offsite dose consequences following a steam generator tube rupture have identified a possible non-conservatism in original FSAR analyses. Post-trip uncovery of the top of the steam generator U-tubes, in conjunction with a break near the U-tube top, could lead to increased iodine release due to a reduced ''scrubbing'' of the iodine in the primary break fluid by the steam generator secondary liquid. To evaluate this issue, analyses were performed at the Idaho National Engineering Laboratory. The RELAP5 computer code was used to conduct an analysis of the Surry plant to determine whether the post-trip steam generator secondary mixture level was sufficient to maintain continuous coverage of the U-tubes. The results indicated continuous coverage of the U-tubes. The RELAP5 result was supported by a hand calculation. Additional RELAP5 analyses were conducted to determine magnitudes of iodine release for a steam generator tube rupture. Two sensitivity studies were conducted. The amount of iodine released to the atmosphere was strongly dependent on the assumed value of the partition coefficient. The assumption of steam generator U-tube uncovery, on a collapsed liquid level basis, following reactor trip had a minor effect on the amount of released iodine. 17 refs., 28 figs., 5 tabs.

Callow, R.A.

1988-10-01T23:59:59.000Z

106

Wafer Preparation and Iodine-Ethanol-Ethanol Passivation Procedure for Reproducible Minority-Carrier Lifetime Measurement: Preprint  

DOE Green Energy (OSTI)

This paper describes reasons that lifetime measurments may be irreproducible using iodine-in-ethanol (I-E) passivation. Possible factors include the strength of the iodine in ethanol solution, wafer cleaning procedures, influence of wafer container during lifetime measurement, and stability of I-E.

Sopori, B.; Rupnowski, P.; Appel, J.; Mehta, V.; Li, C.; Johnston, S.

2008-05-01T23:59:59.000Z

107

“Super Phos” esters: the key to higher-performance products  

Science Conference Proceedings (OSTI)

Robert L. Reierson, winner of the 2012 Samuel Rosen Memorial Award recognizing accomplishments in surfactant chemistry, describes how phosphation process control makes it possible to systematically design and adjust product compositions to deliver maximum

108

Deciphering the measured ratios of Iodine-131 to Cesium-137 at the Fukushima reactors  

E-Print Network (OSTI)

We calculate the relative abundance of the radioactive isotopes Iodine-131 and Cesium-137 produced by nuclear fission in reactors and compare it with data taken at the troubled Fukushima Dai-ichi nuclear power plant. The ratio of radioactivities of these two isotopes can be used to obtain information about when the nuclear reactions terminated.

Matsui, T

2011-01-01T23:59:59.000Z

109

Deciphering the measured ratios of Iodine-131 to Cesium-137 at the Fukushima reactors  

E-Print Network (OSTI)

We calculate the relative abundance of the radioactive isotopes Iodine-131 and Cesium-137 produced by nuclear fission in reactors and compare it with data taken at the troubled Fukushima Dai-ichi nuclear power plant. The ratio of radioactivities of these two isotopes can be used to obtain information about when the nuclear reactions terminated.

T. Matsui

2011-05-02T23:59:59.000Z

110

Features of adsorbed radioactive chemical elements and their isotopes distribution in iodine air filters AU-1500 at nuclear power plants  

E-Print Network (OSTI)

The main aim of research is to investigate the physical features of spatial distribution of the adsorbed radioactive chemical elements and their isotopes in the granular filtering medium in the iodine air filters of the type of AU1500 in the forced exhaust ventilation systems at the nuclear power plant. The gamma activation analysis method is applied to accurately characterize the distribution of the adsorbed radioactive chemical elements and their isotopes in the granular filtering medium in the AU1500 iodine air filter after its long term operation at the nuclear power plant. The typical spectrum of the detected chemical elements and their isotopes in the AU1500 iodine air filter, which was exposed to the bremsstrahlung gamma quantum irradiation, produced by the accelerating electrons in the tantalum target, are obtained. The spatial distributions of the detected chemical element 127I and some other chemical elements and their isotopes in the layer of absorber, which was made of the cylindrical coal granules of the type of SKT3, in the AU1500 iodine air filter are also researched. The possible influences by the standing acoustic wave of air pressure in the iodine air filter on the spatial distribution of the chemical elements and their isotopes in the iodine air filter are discussed. The comprehensive analysis of obtained research results on the distribution of the adsorbed chemical elements and their isotopes in the absorber of iodine air filter is performed.

I. M. Neklyudov; A. N. Dovbnya; N. P. Dikiy; O. P. Ledenyov; Yu. V. Lyashko

2013-06-21T23:59:59.000Z

111

Evaluation of the potential to upgrade the Sandia Atomic Iodine Laser SAIL-1 to higher output energies  

DOE Green Energy (OSTI)

The predicted output energy of the Sandia Atomic Iodine Laser SAIL-1 is given for various numbers of preamplifier stages and for various small signal gains in each stage. Additional possibilities for further increasing the output energy are given.

Riley, M.E.; Palmer, R.E.

1977-05-01T23:59:59.000Z

112

The development of autocatalytic structural materials for use in the sulfur-iodine process for the production of hydrogen  

E-Print Network (OSTI)

The Sulfur-Iodine Cycle for the thermochemical production of hydrogen offers many benefits to traditional methods of hydrogen production. As opposed to steam methane reforming - the most prevalent method of hydrogen ...

Miu, Kevin (Kevin K.)

2006-01-01T23:59:59.000Z

113

Sulfur Iodine Process Summary for the Hydrogen Technology Down-Selection  

DOE Green Energy (OSTI)

This report summarizes the sulfur-iodine (SI) thermochemical water splitting process for the purpose of supporting the process for evaluating and recommending a hydrogen production technology to deploy with the Next Generation Nuclear Plant (NGNP). This package provides the baseline process description as well as a comparison with the process as it was implemented in the Integrated Lab Scale (ILS) experiment conducted at General Atomics from 2006-2009.

Benjamin Russ

2009-05-01T23:59:59.000Z

114

Physical features of accumulation and distribution processes of small disperse coal dust precipitations and absorbed radioactive chemical elements in iodine air filter at nuclear power plant  

E-Print Network (OSTI)

The physical features of absorption process of radioactive chemical elements and their isotopes in the iodine air filters of the type of AU-1500 at the nuclear power plants are researched. It is shown that the non-homogenous spatial distribution of absorbed radioactive chemical elements and their isotopes in the iodine air filter, probed by the gamma-activation analysis method, is well correlated with the spatial distribution of small disperse coal dust precipitations in the iodine air filter. This circumstance points out to an important role by the small disperse coal dust fractions of absorber in the absorption process of radioactive chemical elements and their isotopes in the iodine air filter. The physical origins of characteristic interaction between the radioactive chemical elements and the accumulated small disperse coal dust precipitations in an iodine air filter are considered. The analysis of influence by the researched physical processes on the technical characteristics and functionality of iodine ...

Ledenyov, Oleg P; Poltinin, P Ya; Fedorova, L I

2012-01-01T23:59:59.000Z

115

Ultraviolet photodissociation of iodine monochloride (ICl) at 235, 250, and 265 nm  

SciTech Connect

ICl photolysis in the ultraviolet region of the spectrum (235-265 nm) is studied using the Slice Imaging technique. The Cl*({sup 2}P{sub 1/2})/Cl({sup 2}P{sub 3/2}) and the I*({sup 2}P{sub 1/2})/I({sup 2}P{sub 3/2}) branching ratio between the I({sup 2}P{sub 3/2}) + Cl({sup 2}P{sub 3/2})/Cl*({sup 2}P{sub 1/2}) and I*({sup 2}P{sub 1/2}) + Cl({sup 2}P{sub 3/2})/Cl*({sup 2}P{sub 1/2}) channels is extracted from the respective iodine and chlorine photofragment images. We find that ground state chlorine atoms (Cl({sup 2}P{sub 3/2})) are formed nearly exclusively with excited state iodine atoms (I*({sup 2}P{sub 1/2})), while excited spin-orbit chlorine atoms (Cl*({sup 2}P{sub 1/2})) are concurrently produced only with ground state iodine atoms (I({sup 2}P{sub 3/2})). We conclude that photolysis of ICl in this UV region is a relatively ''clean'' source of spin-orbit excited chlorine atoms that can be used in crossed molecular beam experiments.

Diamantopoulou, N.; Kitsopoulos, Theofanis N. [Institute of Electronic Structure and Laser, Foundation of Research and Technology Hellas, Iraklion 71110 (Greece); Department of Chemistry, University of Crete, Iraklion 71003 (Greece); Kartakoulis, A.; Glodic, P.; Samartzis, Peter C. [Institute of Electronic Structure and Laser, Foundation of Research and Technology Hellas, Iraklion 71110 (Greece)

2011-05-21T23:59:59.000Z

116

Advances in Acid Concentration Membrane Technology for the Sulfur-Iodine Thermochemical Cycle  

DOE Green Energy (OSTI)

One of the most promising cycles for the thermochemical generation of hydrogen is the Sulfur-Iodine (S-I) process, where aqueous HI is thermochemically decomposed into H2 and I2 at approximately 350 degrees Celsius. Regeneration of HI is accomplished by the Bunsen reaction (reaction of SO2, water, and iodine to generate H2SO4 and HI). Furthermore, SO2 is regenerated from the decomposition of H2SO4 at 850 degrees Celsius yielding the SO2 as well as O2. Thus, the cycle actually consists of two concurrent oxidation-reduction loops. As HI is regenerated, co-produced H2SO4 must be separated so that each may be decomposed. Current flowsheets employ a large amount (~83 mol% of the entire mixture) of elemental I2 to cause the HI and the H2SO4 to separate into two phases. To aid in the isolation of HI, which is directly decomposed into hydrogen, water and iodine must be removed. Separation of iodine is facilitated by removal of water. Sulfuric acid concentration is also required to facilitate feed recycling to the sulfuric acid decomposer. Decomposition of the sulfuric acid is an equilibrium limited process that leaves a substantial portion of the acid requiring recycle. Distillation of water from sulfuric acid involves significant corrosion issues at the liquid-vapor interface. Thus, it is desirable to concentrate the acid without boiling. Recent efforts at the INL have concentrated on applying pervaporation through Nafion-117, Nafion-112, and sulfonated poly(etheretherketone) (S-PEEK) membranes for the removal of water from HI/water and HI/Iodine/water feedstreams. In pervaporation, a feed is circulated at low pressure across the upstream side of the membrane, while a vacuum is applied downstream. Selected permeants sorb into the membrane, transport through it, and are vaporized from the backside. Thus, a concentration gradient is established, which provides the driving force for transport. In this work, membrane separations have been performed at temperatures as high as 134 degrees Celsius. Transmembrane fluxes of water are commercially competitive (~5000 g/m2h) and separation factors have been measured as high as 8000, depending on the membrane and the water content. For the Nafion-117 experiments, the common trade off in membrane performance is observed in that as flux is increased, separation factor decreases. Nafion-112, a thinner membrane, exhibited much higher fluxes than the Nafion-117; however without the expected loss in separation factor indicating that the permeability of iodine and HI through Nafion materials is low. Preliminary data for the sulfuric acid concentration suggests performance similar to the HI experiments. All membranes studied for the HI, HI/iodine and sulfuric acid feeds exhibited no degradation in membrane performance during use.

Frederick F. Stewart; Christopher J. Orme

2006-11-01T23:59:59.000Z

117

Fluorine-doped LiNi{sub 0.5}Mn{sub 1.5}O{sub 4} for 5 V cathode materials of lithium-ion battery  

SciTech Connect

Fluorine-doped 5 V cathode materials LiNi{sub 0.5}Mn{sub 1.5}O{sub 4-x}F{sub x} (0.05 {<=} x {<=} 0.2) have been prepared by sol-gel and post-annealing treatment method. The results from X-ray diffraction and scanning electron microscopy (SEM) indicate that the spinel structure changes little after fluorine doping, but the particle size varies with fluorine doping and the preparation conditions. The electrochemical measurements show that stable cycling performance can be obtained when the fluorine amount x is higher than 0.1, but the specific capacity is decreased and 4 V plateau capacity resulting from a conversion of Mn{sup 4+}/Mn{sup 3+} remains. Moreover, influence of the particle size on the reversible capacity of the electrode, especially on the kinetic property, has been examined.

Du Guodong; NuLi, Yanna [Department of Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240 (China); Yang Jun [Department of Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240 (China)], E-mail: yangj723@sjtu.edu.cn; Wang Jiulin [Department of Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240 (China)

2008-12-01T23:59:59.000Z

118

Assessment of Methods to Consolidate Iodine-Loaded Silver-Functionalized Silica Aerogel  

SciTech Connect

The U.S. Department of Energy is currently investigating alternative sorbents for the removal and immobilization of radioiodine from the gas streams in a nuclear fuel reprocessing plant. One of these new sorbents, Ag0-functionalized silica aerogels, shows great promise as a potential replacement for Ag-bearing mordenites because of its high selectivity and sorption capacity for iodine. Moreover, a feasible consolidation of iodine-loaded Ag0-functionalized silica aerogels to a durable SiO2-based waste form makes this aerogel an attractive choice for sequestering radioiodine. This report provides a preliminary assessment of the methods that can be used to consolidate iodine-loaded Ag0-functionalized silica aerogels into a final waste form. In particular, it focuses on experimental investigation of densification of as prepared Ag0-functionalized silica aerogels powders, with or without organic moiety and with or without sintering additive (colloidal silica), with three commercially available techniques: 1) hot uniaxial pressing (HUP), 2) hot isostatic pressing (HIP), and 3) spark plasma sintering (SPS). The densified products were evaluated with helium gas pycnometer for apparent density, with the Archimedes method for apparent density and open porosity, and with high-resolution scanning electron microscopy and energy dispersive spectroscopy (SEM-EDS) for the extent of densification and distribution of individual elements. The preliminary investigation of HUP, HIP, and SPS showed that these sintering methods can effectively consolidate powders of Ag0-functionalized silica aerogel into products of near-theoretical density. Also, removal of organic moiety and adding 5.6 mass% of colloidal silica to Ag0-functionalized silica aerogel powders before processing provided denser products. Furthermore, the ram travel data for SPS indicated that rapid consolidation of powders can be performed at temperatures below 950°C.

Matyas, Josef; Engler, Robert K.

2013-09-01T23:59:59.000Z

119

Stepwise computational synthesis of fullerene C{sub 60} derivatives. Fluorinated fullerenes C{sub 60}F{sub 2k}  

Science Conference Proceedings (OSTI)

Reactions of fullerene C{sub 60} with atomic fluorine are studied by the unrestricted broken spin symmetry Hartree-Fock (UBS HF) approach implemented in semiempirical codes based on the AMI technique. The calculations are focused on a successive addition of a fluorine atom to the fullerene cage following the indication of the highest chemical susceptibility of the cage atom, which is calculated at each step. The proposed computational synthesis is based on the effectively unpaired-electron concept of the chemical susceptibility of fullerene atoms. The obtained results are analyzed from the standpoints of energy, symmetry, and the composition abundance. A good fitting of the data to experimental findings proves a creative role of the suggested synthetic methodology.

Sheka, E. F., E-mail: sheka@icp.ac.r [Peoples' Friendship University of Russia, General Physics Department (Russian Federation)

2010-09-15T23:59:59.000Z

120

Effect of Dietary Intake of Stable Iodine on Dose-per-unit-intake Factors for 99Tc  

SciTech Connect

It is well-known that the human thyroid concentrates iodine more than 100 times the concentration in plasma. Also well-known is the fact that large amounts of stable iodine in the diet can limit thyroid uptake of total iodine; this is the basis for administering potassium iodide following a release of radioiodine from a nuclear reactor accident or nuclear weapon detonation. Many researchers have shown enhanced concentrations of both organic and inorganic iodine in saliva and breast milk. Technetium-99 is a long-lived (231,000 year half-life) radionuclide of concern in the management of high-level radioactive waste. There is no doubt that 99Tc, if it is in groundwater, will be found in the chemical form of pertechnetate, 99TcO4?. Pertechnetate is a large anion, almost identical in size to iodide, I?. The nuclear medicine literature shows that pertechnetate concentrates in the thyroid, salivary glands, and lactating breast in addition to the stomach, liver, and alimentary tract as currently recognized by the International Commission on Radiological Protection (ICRP). The fact that large intakes of stable iodine (127I) in the diet limit uptake of iodine by the thyroid leads one to generalize that stable iodine in the diet may also limit thyroid uptake of pertechnetate. While there is at least one report that iodine in the diet blocks uptake of 99mTcO4? by the thyroid and salivary glands (which have the same Na/I symporter, the biochemical concentration mechanism), the level of protective effect seen for blocking radioactive iodine is not expected for 99TcO4? because pertechnetate does not become organically bound in the thyroid and thus is not retained for months the way iodide is. While it does account for Tc concentration in the thyroid, the existing ICRP biokinetic model for technetium does not take enhanced concentrations in salivary gland and breast tissue into account. From the survey of the nuclear medicine literature, it is not possible to compute the effect of stable iodine in the diet on the dose per unit intake factors for 99Tc without developing an improved biokinetic model for technetium. Specific experiments should be designed to quantitatively evaluate 99TcO4? metabolism, excretion, and secretion, as well as to evaluate its chemical toxicity It is recommended that the ICRP reexamine its biokinetics models for Tc based on nuclear medicine data that have accumulated over the years. In particular, the ICRP ignores the lactation pathway, the enhanced concentration of Tc in breast and breast milk, and enhanced concentration of Tc (and I) in the salivary glands as well as in the thyroid. The ICRP should also explicitly incorporate the effect of stable iodine in the diet into both its models for iodine and technetium. The effect of concentration of Tc in breast milk needs further study for dosimetric implications to nursing infants whose mothers may ingest 99TcO4? from groundwater sources. The ICRP should also investigate the possibility of enhanced concentration of both I and Tc in the non-lactating female breast. To do these re-evaluations of biokinetic models, new experiments designed specifically to evaluate these questions concerning the biokinetics of Tc and I are needed.

Strom, Daniel J.

2003-09-30T23:59:59.000Z

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


121

LITERATURE SURVEY FOR GROUNDWATER TREATMENT OPTIONS FOR NITRATE IODINE-129 AND URANIUM 200-ZP-1 OPERABLE UNIT HANFORD SITE  

SciTech Connect

This literature review presents treatment options for nitrate, iodine-129, and uranium, which are present in groundwater at the 200-ZP-I Groundwater Operable Unit (OU) within the 200 West Area of the Hanford Site. The objective of this review is to determine available methods to treat or sequester these contaminants in place (i.e., in situ) or to pump-and-treat the groundwater aboveground (i.e., ex situ). This review has been conducted with emphasis on commercially available or field-tested technologies, but theoretical studies have, in some cases, been considered when no published field data exist. The initial scope of this literature review included only nitrate and iodine-I 29, but it was later expanded to include uranium. The focus of the literature review was weighted toward researching methods for treatment of nitrate and iodine-129 over uranium because of the relatively greater impact of those compounds identified at the 200-ZP-I OU.

BYRNES ME

2008-06-05T23:59:59.000Z

122

Scoping calculation for components of the cow-milk dose pathway for evaluating the dose contribution from iodine-131  

Science Conference Proceedings (OSTI)

A series of scoping calculations have been undertaken to evaluate The absolute and relative contribution of different exposure pathways to doses that may have been received by individuals living in the vicinity of the Hanford site. This scoping calculation (Calculation 001) examined the contributions of the various exposure pathways associated with environmental transport and accumulation of iodine-131 in the pasture-cow-milk pathway. Addressed in this calculation were the contributions to thyroid dose of infants and adult from (1) the ingestion by dairy cattle of various feedstuffs (pasturage, silage, alfalfa hay, and grass hay) in four different feeding regimes; (2) ingestion of soil by dairy cattle; (3) ingestion of stared feed on which airborne iodine-131 had been deposited; and (4) inhalation of airborne iodine-131 by dairy cows.

Ikenberry, T.A.; Napier, B.A.

1992-12-01T23:59:59.000Z

123

Similarity criteria in calculations of the energy characteristics of a cw oxygen - iodine laser  

SciTech Connect

The calculated and experimental data on the energy efficiency of a cw oxygen - iodine laser (OIL) are analysed based on two similarity criteria, namely, on the ratio of the residence time of the gas mixture in the resonator to the characteristic time of extraction of the energy stored in singlet oxygen td and on the gain-to-loss ratio {Pi}. It is shown that the simplified two-level laser model satisfactorily predicts the output characteristics of OILs with a stable resonator at {tau}{sub d} {<=} 7. Efficient energy extraction from the OIL active medium is achieved in the case of {tau}{sub d} = 5 - 7, {Pi} = 4 - 8. (lasers)

Mezhenin, A V; Azyazov, V N

2012-12-31T23:59:59.000Z

124

Test bench for studying the outlook for industrial applications of an oxygen-iodine laser  

Science Conference Proceedings (OSTI)

We report the development and tests of a chemical oxygen-iodine laser test bench based on a twisted-aerosol-flow singlet-oxygen generator and a supersonic laser model for studying the outlook for industrial applications of this laser. The maximal output power of the laser is {approx}65 kW (the average power is {approx}50 kW), corresponding to a specific output power of {approx}110 W cm{sup -2}. The maximal chemical efficiency is {approx}34%. (letters)

Adamenkov, A A; Bakshin, V V; Bogachev, A V; Buryak, E V; Vdovkin, L A; Velikanov, S D; Vyskubenko, B A; Garanin, Sergey G; Gorbacheva, E V; Grigorovich, Sergei V; Il'in, S P; Il'kaev, R I; Ilyushin, Yurii N; Kalashnik, A M; Kolobyanin, Yu V; Leonov, M L; Svischev, V V; Troshkin, M V [Russian Federal Nuclear Center 'All-Russian Scientific Research Institute of Experimental Physics', Sarov, Nizhnii Novgorod Region (Russian Federation)

2007-07-31T23:59:59.000Z

125

Sulfur Iodine Process Summary for the Hydrogen Technology Down-Selection: Process Performance Package  

DOE Green Energy (OSTI)

This document describes the details of implementing a Sulfur-Iodine (S-I) hydrogen production plant to deploy with the Next General Nuclear Power Plant (NGNP). Technical requirements and specifications are included, and a conceptual plant design is presented. The following areas of interest are outlined in particular as a baseline for the various technology comparisons: (1) Performance Criteria - (a) Quantity of hydrogen produced, (b) Purity of hydrogen produced, (c) Flexibility to serve various applications, (d) Waste management; (2) Economic Considerations - (a) Cost of hydrogen, (b) Development costs; and (3) Risk - (a) Technical maturity of the S-I process, (b) Development risk, (c) Scale up options.

Benjamin Russ

2009-06-01T23:59:59.000Z

126

Methods of Gas Phase Capture of Iodine from Fuel Reprocessing Off-Gas: A Literature Survey  

SciTech Connect

A literature survey was conducted to collect information and summarize the methods available to capture iodine from fuel reprocessing off-gases. Techniques were categorized as either wet scrubbing or solid adsorbent methods, and each method was generally described as it might be used under reprocessing conditions. Decontamination factors are quoted only to give a rough indication of the effectiveness of the method. No attempt is made to identify a preferred capture method at this time, although activities are proposed that would provide a consistent baseline that would aid in evaluating technologies.

Daryl Haefner

2007-02-01T23:59:59.000Z

127

Development of a dynamic simulation code for the sulfur-iodine process coupled to a very high-temperature gas-cooled nuclear reactor  

Science Conference Proceedings (OSTI)

One of the key issues in developing a sulfur-iodine (SI) thermochemical hydrogen production technology is how to operate the SI process, including the start-up operation procedure. In order to effectively establish a start-up procedure, it is necessary ... Keywords: dynamic simulation, nuclear hydrogen, start-up, sulfur-iodine process, very high-temperature gas-cooled reactor

Jiwoon Chang, Youngjoon Shin, Kiyoung Lee, Yongwan Kim, Cheong Youn

2013-02-01T23:59:59.000Z

128

Potential influence of iodine-containing compounds on the chemistry of the troposphere in the polar spring. I. Ozone depletion  

Science Conference Proceedings (OSTI)

Iodine in the atmosphere, identified largely by the presence of IO, is a ubiquitous component of the troposphere in coastal and oceanic areas. The role, if any, that iodine chemistry plays in the polar ozone depletion episodes is not known. These events are rationalized today largely in terms of Br2- and BrCl-initiated reactions. The potential for enhancement of ozone depletions through the presence of iodine-containing molecules (I{sub 2}, IBr, ICl, CH{sub 2}I{sub 2}, CH{sub 2}IBr, CH{sub 2}ICl, and CH{sub 3}I) is investigated in this study. Computer simulations of the homogeneous chemistry are made using a reasonably complete reaction mechanism for Br-, Cl- and I-containing species together with representative chemistry of trace gases in the clean troposphere. The extent of uncertain alternative pathways and efficiencies for OIO and I{sub 2}O{sub 2} photolyses are varied over a range of possible values to establish the sensitivity of the depletion events to these variables. The study shows that significant enhancements of the polar ozone depletion are expected when small amounts of iodine-containing compounds such as CH{sub 2}I{sub 2}, IBr, or ICl are present in a polar air mass containing representative Br{sub 2}-BrCl-trace gas mixtures. The synergistic effect of the iodine compounds results from additional halogen-atom formation from IO-IO, IO-BrO, and IO-ClO reactions. Measurements of IO and precursor iodine-containing compounds are encouraged for future polar spring studies, as well as currently acknowledged important trace species (O{sub 3}, CH{sub 2}O, BrO, Br{sub 2}, and BrCl).

Calvert, Jack G [ORNL; Lindberg, Steven Eric [ORNL

2004-05-01T23:59:59.000Z

129

Generation of concentration density maxima of small dispersive coal dust particles in horizontal iodine air filter at air-dust aerosol blow  

E-Print Network (OSTI)

The spatial distributions of the small dispersive coal dust particles with the nano and micro sizes in the granular filtering medium with the cylindrical coal granules in the absorber in the horizontal iodine air filter during its long term operation at the nuclear power plant are researched. It is shown that the concentration density maxima of the small dispersive coal dust particles appear in the granular filtering medium with the cylindrical coal absorbent granules in the horizontal iodine air filter at an action by the air dust aerosol blow. The comparison of the measured aerodynamic resistances of the horizontal and vertical iodine air filters is conducted. The main conclusion is that the magnitude of the aerodynamic resistance of the horizontal iodine air filters is much smaller in comparison with the magnitude of the aerodynamic resistance of the vertical iodine air filters at the same loads of the air dust aerosol volumes. It is explained that the direction of the air dust aerosol blow and the direction of the gravitation force in the horizontal iodine air filter are orthogonal, hence the effective accumulation of the small dispersive coal dust particles takes place at the bottom of absorber in the horizontal iodine air filter. It is found that the air dust aerosol stream flow in the horizontal iodine air filter is not limited by the appearing structures, made of the precipitated small dispersive coal dust particles, in distinction from the vertical iodine air filter, in the process of long term operation of the iodine air filters at the nuclear power plant.

I. M. Neklyudov; O. P. Ledenyov; L. I. Fedorova; P. Ya. Poltinin

2013-06-11T23:59:59.000Z

130

Radioimmunoguided surgery using iodine 125 B72. 3 in patients with colorectal cancer  

SciTech Connect

Preliminary data using B72.3 murine monoclonal antibody labeled with iodine 125 suggested that both clinically apparent as well as occult sites of colorectal cancer could be identified intraoperatively using a hand-held gamma detecting probe. We report the preliminary data of a multicenter trial of this approach in patients with primary or recurrent colorectal cancer. One hundred four patients with primary, suspected, or known recurrent colorectal cancer received an intravenous infusion of 1 mg of B72.3 monoclonal antibody radiolabeled with 7.4 x 10 Bq of iodine 125. Twenty-six patients with primary colorectal cancer and 72 patients with recurrent colorectal cancer were examined. Using the gamma detecting probe, 78% of the patients had localization of the antibody in their tumor; this included 75% of primary tumor sites and 63% of all recurrent tumor sites; 9.2% of all tumor sites identified represented occult sites detected only with the gamma detecting probe. The overall sensitivity was 77% and a predictive value of a positive detection was 78%. A total of 30 occult sites in 26 patients were identified. In patients with recurrent cancer, the antibody study provided unique data that precluded resection in 10 patients, and in another eight patients it extended the potentially curative procedure.

Cohen, A.M.; Martin, E.W. Jr.; Lavery, I.; Daly, J.; Sardi, A.; Aitken, D.; Bland, K.; Mojzisik, C.; Hinkle, G. (Memorial Sloan-Kettering Cancer Center, New York, NY (USA))

1991-03-01T23:59:59.000Z

131

Radioactive iodine treatment of a functional thyroid carcinoma producing hyperthyroidism in a dog  

SciTech Connect

Radioactive iodine (/sup 131/I) was used in the treatment of a 12-year-old female dog with hyperthyroidism resulting from a large, unresectable (and metastatic) thyroid carcinoma associated with signs of severe inspiratory stridor and dyspnea. Hyperthyroidism was diagnosed on the basis of clinical signs (polyuria, polydipsia, polyphagia, weight loss, nervousness) and high basal serum thyroxine (T4) concentrations, as well as thyroid radioiodine kinetic studies that showed a high radioiodine uptake into the thyroid (% thyroid uptake) and markedly increased serum concentrations of protein-bound iodine-131 (PB/sup 131/I) after /sup 131/I tracer injection. Thyroid imaging revealed diffuse radionuclide accumulation by the tumor, which involved both thyroid lobes. The dog was treated with three large doses of radioiodine (/sup 131/I), ranging from 60 to 75 mCi, given at intervals of 5 to 7 months. The dog became euthyroid, and the size of the tumor decreased by approximately 25% after each /sup 131/I treatment, improving the severe inspiratory stridor and dyspnea, but both the hyperthyroid state and breathing difficulty recurred within a few months of each treatment. The dog was euthanatized 5 months after the last treatment because of progressive tracheal compression and pulmonary metastasis.

Peterson, M.E.; Kintzer, P.P.; Hurley, J.R.; Becker, D.V.

1989-01-01T23:59:59.000Z

132

Roles of Naturally Occurring Bacteria in Controlling Iodine-129 Mobility in Subsurface Soils  

E-Print Network (OSTI)

129I is of major concern because of its biophilic nature, excessive inventory, long half-life (~16 million yrs), and high mobility in the natural environment that depends on its chemical speciation. Iodide (I-) has the highest mobility than iodate (IO3-) and is the predominant species in the terrestrial environment due to prevailing pH and Eh conditions. In order to transform I- to less mobile organo-iodine (OI), strong oxidants are necessary to activate the first electron transfer step from I- to reactive intermediates. The aim of this study was to determine the influence of naturally occurring aerobic bacteria isolated from an 129I contaminated aquifer (F-area of the Savannah River Site, SC) on I- oxidation and OI formation. It was demonstrated that 3 of 136 strains accumulated I- (0.2~2%) in the presence of H2O2, when incubated in the presence of an environmentally relevant concentration of I- (0.1 microM). The accumulation was likely through electrophilic substitution resulting in the iodination of cellular constituents. The results indicated that culturable I--accumulating bacteria are not directly responsible for the high fraction of oxidized iodine species (IO3- and OI, >50% of total I) present in the SRS F-area. Several bacterial strains were found to be capable of stimulating I- oxidation through excretion of oxidants and enzymes. Organic acids in spent liquid medium from 27 of 84 aerobic bacterial cultures enhanced H2O2-dependent I- oxidation 2-10 fold. Organic acids enhanced I- oxidation by (1) lowering the pH of the spent medium and (2) reacting with H2O2 to form peroxy carboxylic acids, which are strong oxidizing agents. In the absence of H2O2, spent medium from 44 of 84 bacteria cultures showed I- oxidizing capacities. One I- oxidizing bacterium was studied to characterize its extracellular I- oxidizing component(s). The I- oxidizing capability from the spent medium was inactive by treatments with heat and H2O2 and absent under anaerobic conditions. Conversely, NADH, NADPH and FMN additions stimulated I- oxidation in the spend medium. These results indicate an oxidase(s) catalyzed I- oxidation. Understanding the bacterial activities involved with I- oxidation and OI formation is expected to help reduce 129I mobility in water-soil systems.

Li, Hsiu-Ping

2012-08-01T23:59:59.000Z

133

Stable n-CuInSe/sub 2/iodide-iodine photoelectrochemical cell  

DOE Patents (OSTI)

In a photoelectrochemical solar cell, stable output and solar efficiency in excess of 10% are achieved with a photoanode of n-CuInSe/sub 2/ electrode material and an iodine/iodide redox couple used in a liquid electrolyte. The photoanode is prepared by treating the electrode material by chemical etching, for example in Br/sub 2//MeOH; heating the etched electrode material in air or oxygen; depositing a surface film coating of indium on the electrode material after the initial heating; and thereafter again heating the electrode material in air or oxygen to oxidize the indium. The electrolyte is treated by the addition of Cu/sup +/ or Cu/sup 2 +/ salts and in In/sup 3 +/ salts.

Cahen, D.; Chen, Y.W.

1984-09-20T23:59:59.000Z

134

Stable N-CuInSe.sub.2 /iodide-iodine photoelectrochemical cell  

DOE Patents (OSTI)

In a photoelectrochemical solar cell, stable output and solar efficiency in excess of 10% are achieved with a photoanode of n-CuInSe.sub.2 electrode material and an iodine/iodide redox couple used in a liquid electrolyte. The photoanode is prepared by treating the electrode material by chemical etching, for example in Br.sub.2 /MeOH; heating the etched electrode material in air or oxygen; depositing a surface film coating of indium on the electrode material after the initial heating; and thereafter again heating the electrode material in air or oxygen to oxidize the indium. The electrolyte is treated by the addition of Cu.sup.+ or Cu.sup.2+ salts and In.sup.3+ salts.

Cahen, David (Rehovot, IL); Chen, Yih W. (Lakewood, CO)

1985-01-01T23:59:59.000Z

135

The Sulfur-Iodine Cycle: Process Analysis and Design Using Comprehensive Phase Equilibrium Measurements and Modeling  

DOE Green Energy (OSTI)

Of the 100+ thermochemical hydrogen cycles that have been proposed, the Sulfur-Iodine (S-I) Cycle is a primary target of international interest for the centralized production of hydrogen from nuclear power. However, the cycle involves complex and highly nonideal phase behavior at extreme conditions that is only beginning to be understood and modeled for process simulation. The consequence is that current designs and efficiency projections have large uncertainties, as they are based on incomplete data that must be extrapolated from property models. This situation prevents reliable assessment of the potential viability of the system and, even more, a basis for efficient process design. The goal of this NERI award (05-006) was to generate phase-equilibrium data, property models, and comprehensive process simulations so that an accurate evaluation of the S-I Cycle could be made. Our focus was on Section III of the Cycle, where the hydrogen is produced by decomposition of hydroiodic acid (HI) in the presence of water and iodine (I2) in a reactive distillation (RD) column. The results of this project were to be transferred to the nuclear hydrogen community in the form of reliable flowsheet models for the S-I process. Many of the project objectives were achieved. At Clemson University, a unique, tantalum-based, phase-equilibrium apparatus incorporating a view cell was designed and constructed for measuring fluid-phase equilibria for mixtures of iodine, HI, and water (known as HIx) at temperatures to 350 °C and pressures to 100 bar. Such measurements were of particular interest for developing a working understanding of the expected operation of the RD column in Section III. The view cell allowed for the IR observation and discernment of vapor-liquid (VL), liquid-liquid, and liquid-liquid-vapor (LLVE) equilibria for HIx systems. For the I2-H2O system, liquid-liquid equilibrium (LLE) was discovered to exist at temperatures up to 310-315 °C, in contrast to the models and predictions of earlier workers. For the I2-HI-H2O ternary, LLE and LLVE were all observed for the first time at temperatures of 160 and 200 °C. Three LLE tie-lines were measured at 160 °C, and preliminary indications are that the underlying phase behavior could result in further improvements in the performance of the S-I Cycle. Unfortunately, these new results were obtained too late in the project to be incorporated into the modeling and simulation work described below. At the University of Virginia, a uniquely complete and reliable model was developed for the thermodynamic properties of HIx, covering the range of conditions expected for the separation of product hydrogen and recycled iodine in the RD column located in Section III. The model was validated with all available property spectroscopy data. The results provide major advances over prior understanding of the chemical speciation involved. The model was implemented in process simulation studies of the S-I Cycle, which showed improvement in energy efficiency to 42%, as well as significantly smaller capital requirements due to lower pressure operation and much smaller equipment sizes. The result is that the S-I Cycle may be much more economically feasible than was previously thought. If both the experimental and modeling work described above were to be continued to ultimate process optimization, both the American public and the global community would benefit from this alternative energy source that does not produce carbon emissions.

Thies, Mark C.; O'Connell, J. P.; Gorensek, Maximilian B.

2010-01-10T23:59:59.000Z

136

Determination of the Relative Amount of Fluorine in Uranium Oxyfluoride Particles using Secondary Ion Mass Spectrometry and Optical Spectroscopy  

Science Conference Proceedings (OSTI)

Both nuclear forensics and environmental sampling depend upon laboratory analysis of nuclear material that has often been exposed to the environment after it has been produced. It is therefore important to understand how those environmental conditions might have changed the chemical composition of the material over time, particularly for chemically sensitive compounds. In the specific case of uranium enrichment facilities, uranium-bearing particles stem from small releases of uranium hexafluoride, a highly reactive gas that hydrolyzes upon contact with moisture from the air to form uranium oxyfluoride (UO{sub 2}F{sub 2}) particles. The uranium isotopic composition of those particles is used by the International Atomic Energy Agency (IAEA) to verify whether a facility is compliant with its declarations. The present study, however, aims to demonstrate how knowledge of time-dependent changes in chemical composition, particle morphology and molecular structure can contribute to an even more reliable interpretation of the analytical results. We prepared a set of uranium oxyfluoride particles at the Institute for Reference Materials and Measurements (IRMM, European Commission, Belgium) and followed changes in their composition, morphology and structure with time to see if we could use these properties to place boundaries on the particle exposure time in the environment. Because the rate of change is affected by exposure to UV-light, humidity levels and elevated temperatures, the samples were subjected to varying conditions of those three parameters. The NanoSIMS at LLNL was found to be the optimal tool to measure the relative amount of fluorine in individual uranium oxyfluoride particles. At PNNL, cryogenic laser-induced time-resolved U(VI) fluorescence microspectroscopy (CLIFS) was used to monitor changes in the molecular structure.

Kips, R; Kristo, M J; Hutcheon, I D; Amonette, J; Wang, Z; Johnson, T; Gerlach, D; Olsen, K B

2009-05-29T23:59:59.000Z

137

Wafer Preparation and Iodine-Ethanol Passivation Procedure for Reproducible Minority-Carrier Lifetime Measurement (Poster)  

DOE Green Energy (OSTI)

Measurement of the bulk minority-carrier lifetime (T{sub b}) by optical methods, such as photocurrent decay or quasi-steady-state photoconductance (QSSPC), is strongly influenced by surface recombination. Several techniques are known to lower the effective surface recombination velocity, including the following: use of oxidation, floating N/P junction, SiN:H layer, HF immersion, and use of iodine in ethanol or methanol (I-E solution). Using I-E appears to be very simple and does not require any high-temperature treatment such as oxidation, diffusion, or nitridation processes, which can change T{sub b}. However, this is not a preferred procedure within the photovoltaic community because it is difficult to obtain same T{sub b} values reproducibly, particularly when the wafer lifetime is long. The objectives are: (1) Investigate various reasons why lifetime measurements may be irreproducible using I-E solution passivation. (2) Study the influence of the strength of iodine in the ethanol solution, wafer-cleaning procedures, influence of the wafer container during lifetime measurements, and the stability of I-E. (3) Compare lifetimes of wafers (having different T{sub b}) by various techniques such as QSSPC and transient photoconductive decay using short laser pulses of different light intensity; (4) Make minority-carrier diffusion length (L) measurements by a surface photovoltage technique, and to use T{sub b} and L data to determine diffusivity (D) values for various impurity and defect concentrations, using the relationship L{sup 2} = D* T{sub b}.

Sopori, B.; Rupnowski, P.; Appel, J.; Mehta, V.; Li, C.; Johnston, S.

2008-05-01T23:59:59.000Z

138

Influence by small dispersive coal dust particles of different fractional consistence on characteristics of iodine air filter at nuclear power plant  

E-Print Network (OSTI)

The main purpose of research is to determine the influence by the small dispersive coal dust particles of the different fractional consistence on the technical characteristics of the vertical iodine air filter at nuclear power plant. The research on the transport properties of the small dispersive coal dust particles in the granular filtering medium of absorber in the vertical iodine air filter is completed in the case, when the modeled aerodynamic conditions are similar to the real aerodynamic conditions. It is shown that the appearance of the different fractional consistence of small dispersive coal dust particles with the decreasing dimensions down to the micro and nano sizes at the action of the air dust aerosol stream normally results in a significant change of distribution of the small dispersive coal dust particles masses in the granular filtering medium of an absorber in the vertical iodine air filter, changing the vertical iodine air filter aerodynamic characteristics. The precise characterization of...

Neklyudov, I M; Fedorova, L I; Poltinin, P Ya

2013-01-01T23:59:59.000Z

139

Influence by small dispersive coal dust particles of different fractional consistence on characteristics of iodine air filter at nuclear power plant  

E-Print Network (OSTI)

The main purpose of research is to determine the influence by the small dispersive coal dust particles of the different fractional consistence on the technical characteristics of the vertical iodine air filter at nuclear power plant. The research on the transport properties of the small dispersive coal dust particles in the granular filtering medium of absorber in the vertical iodine air filter is completed in the case, when the modeled aerodynamic conditions are similar to the real aerodynamic conditions. It is shown that the appearance of the different fractional consistence of small dispersive coal dust particles with the decreasing dimensions down to the micro and nano sizes at the action of the air dust aerosol stream normally results in a significant change of distribution of the small dispersive coal dust particles masses in the granular filtering medium of an absorber in the vertical iodine air filter, changing the vertical iodine air filter aerodynamic characteristics. The precise characterization of the aerodynamic resistance of a model of the vertical iodine air filter is completed. The comparative analysis of the technical characteristics of the vertical and horizontal iodine air filters is also made.

I. M. Neklyudov; O. P. Ledenyov; L. I. Fedorova; P. Ya. Poltinin

2013-02-18T23:59:59.000Z

140

Screening Protocol for Iodine-Specific Getters in YMP-Related Invert Applications  

SciTech Connect

This document defines a standardized screening protocol for use in developing iodine ''getters'' for placement in the proposed YMP-repository invert. The work was funded by the US Department of Energy (DOE), Office of Civilian Radioactive Waste Management (OCRWM), Office of Science and Technology International (S&T) during 2004-2005. First, the likely environmental conditions in the invert are reviewed as a basis for defining the thermal and geochemical regimes in which a getter must function. These considerations, then, served as the basis for laying out a hierarchy of materials screening tests (Table 1). An experimental design for carrying out these screening tests follows next. Finally, the latter half of the document develops methods for preparing test solutions with chemistries that relate to various aspects of the YMP-repository environment (or, at least to such representations as were available from program documents late in 2004). Throughout the document priority was given to defining procedures that would quickly screen out unpromising candidate materials with a minimum amount of labor. Hence, the proposed protocol relies on batch tests over relatively short times, and on a hierarchy of short pre-test conditioning steps. So as not to repeat the mistakes (and frustrations) encountered in the past (notably in preparing WIPP test brines) particular care was also given to developing standardized test solution recipes that could be prepared easily and reproducibly. This document is principally intended for use as a decision-making tool in evaluating and planning research activities. It is explicitly NOT a roadmap for qualifying getters for actual placement in the repository. That would require a comprehensive test plan and a substantial consensus building effort. This document is also not intended to provide a complete list of all the tests that individuals may wish to carry out. Various materials will have their own peculiar concerns that will call for additional specialized tests. In many cases additional research will also be needed to verify the exact nature of the chemical process responsible for scavenging the iodine from the test solutions.

J.L. Krumhansl; J.D. Pless; J.B. Chwirka

2006-07-17T23:59:59.000Z

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


141

Screening protocol for iodine-specific getters in YMP-related invert applications.  

Science Conference Proceedings (OSTI)

This document defines a standardized screening protocol for use in developing iodine ''getters'' for placement in the proposed YMP-repository invert. The work was funded by the US Department of Energy (DOE), Office of Civilian Radioactive Waste Management (OCRWM), Office of Science and Technology International (S&T) during 2004-2005. First, the likely environmental conditions in the invert are reviewed as a basis for defining the thermal and geochemical regimes in which a getter must function. These considerations, then, served as the basis for laying out a hierarchy of materials screening tests (Table 1). An experimental design for carrying out these screening tests follows next. Finally, the latter half of the document develops methods for preparing test solutions with chemistries that relate to various aspects of the YMP-repository environment (or, at least to such representations as were available from program documents late in 2004). Throughout the document priority was given to defining procedures that would quickly screen out unpromising candidate materials with a minimum amount of labor. Hence, the proposed protocol relies on batch tests over relatively short times, and on a hierarchy of short pre-test conditioning steps. So as not to repeat the mistakes (and frustrations) encountered in the past (notably in preparing WIPP test brines) particular care was also given to developing standardized test solution recipes that could be prepared easily and reproducibly. This document is principally intended for use as a decision-making tool in evaluating and planning research activities. It is explicitly NOT a roadmap for qualifying getters for actual placement in the repository. That would require a comprehensive test plan and a substantial consensus building effort. This document is also not intended to provide a complete list of all the tests that individuals may wish to carry out. Various materials will have their own peculiar concerns that will call for additional specialized tests. In many cases additional research will also be needed to verify the exact nature of the chemical process responsible for scavenging the iodine from the test solutions.

Krumhansl, James Lee; Pless, Jason; Chwirka, J. Benjamin

2006-07-01T23:59:59.000Z

142

REFINING FLUORINATED COMPOUNDS  

DOE Patents (OSTI)

This invention relates to the method of refining a liquid perfluorinated hydrocarbon oil containing fluorocarbons from 12 to 28 carbon atoms per molecule by distilling between 150 deg C and 300 deg C at 10 mm Hg absolute pressure. The perfluorinated oil is washed with a chlorinated lower aliphatic hydrocarbon, which mairtains a separate liquid phase when mixed with the oil. Impurities detrimental to the stability of the oil are extracted by the chlorinated lower aliphatic hydrocarbon. (AEC)

Linch, A.L.

1963-01-01T23:59:59.000Z

143

Fluorine-containing - Springer  

Science Conference Proceedings (OSTI)

J. F. King and T. Durst, Can. J. Chem., 44, 819 (1966). L. I. Ragulin, P. P. Ropalo ... of Study o[ Organic Compounds [in Rus- sian], Vol. 2, Goskhimizdat (1952), p.

144

FLUORINE CELL ANODE ASSEMBLY  

DOE Patents (OSTI)

An improved anode assembly is deslgned for use in electrolytlc cells ln the productlon of hydrogen and fluorlne from a moIten electrolyte. The anode assembly comprises a copper post, a copper hanger supported by the post, a plurality of carbon anode members, and bolt means for clamplng half of the anode members to one slde of the hanger and for clamplng the other half of the anode members to the other slde of the hanger. The heads of the clamplng bolts are recessed withln the anode members and carbon plugs are inserted ln the recesses above the bolt heads to protect the boIts agalnst corroslon. A copper washer is provided under the head of each clamplng boIt such that the anode members can be tightly clamped to the hanger with a resultant low anode jolnt resistance. (AEC)

Cable, R.E.; Goode, W.B. Jr.; Henderson, W.K.; Montillon, G.H.

1962-06-26T23:59:59.000Z

145

Serum thyroxine concentrations after radioactive iodine therapy in cats with hyperthyroidism  

SciTech Connect

Thirty-one cats with hyperthyroidism were given one dose of radioactive iodine (131I) IV. Serum thyroxine (T4) concentrations were measured before treatment in all cats, at 12-hour intervals after treatment in 10 cats, and at 48-hour intervals after treatment in 21 cats. Serum T4 concentrations also were measured one month after /sup 131/I therapy in 29 cats. Activity of 131I administered was 1.5 to 6.13 mCi, resulting in a dose of 20,000 rads to the thyroid. Serum T4 concentrations before /sup 131/I administration were 5.3 to 51.0 micrograms/dl, with a median T4 concentration of 11.0 micrograms/dl. Serum T4 decreased most rapidly during the first 3 to 6 days after treatment. Sixteen cats (55%) had normal serum thyroxine concentrations by day 4 after 131I administration, and 23 cats (74%) were euthyroxinemic by day 8 after treatment. One month after administration of 131I, the 29 cats evaluated were clinically improved, and 24 (83%) of the 29 cats evaluated had normal serum T4 concentrations, 3 cats (10%) remained hyperthyroxinemic, and 2 cats (7%) were hypothyroxinemic. Therefore, administration of 131I was a safe and effective method to quickly decrease serum T4 concentrations in hyperthyroid cats.

Meric, S.M.; Hawkins, E.C.; Washabau, R.J.; Turrel, J.M.; Feldman, E.C.

1986-05-01T23:59:59.000Z

146

Recovery of Technetium and Iodine from Spent ATW TRISO Type Fuels.  

SciTech Connect

The Accelerator Transmutation of Waste (ATW) program is being developed to determine the feasibility of separating and transmutating the transactinides (Pu-Cm) and long-lived fission product (99Tc and 129I) from spent LWR fuel. Several types of ATW fuels have been suggested to transmutate the Pu-Cm fraction including TRISO type fuels. An ATW TRISO fuel would consist of a Pu-Cm oxide kernel surrounded by several layers of pyrolytic carbon, a layer of SiC, and an outer layer of pyrolytic carbon. Processing of the spent ATW fuel would involve the crush, burn, and leach approach used on normal TRISO fuels. This report describes experiments that determine the potential behavior of the two long-lived fission products, 99Tc and 129I, in this processing. Iodine can be removed and trapped during the burning of the carbon from the fuel. Some technetium may volatilize in the latter stages of the burn but the bulk of it will have to be recovered after dissolution of the oxide residue.

Schroeder, N. C. (Norman C.); Attrep, Moses

2001-01-01T23:59:59.000Z

147

Chalcogen-based aerogels as a multifunctional platform for remediation of radioactive iodine  

Science Conference Proceedings (OSTI)

Aerogels employing chalcogen-based (i.e., S, Se, and/or Te) structural units and interlinking metals are termed chalcogels and have many emerging applications. Here, chalcogels are discussed in the context of nuclear fuel reprocessing and radioactive waste remediation. Motivated by previous work on removal of heavy metals in aqueous solution, we explored the application of germanium sulfide chalcogels as a sorbent for gas-phase I2 based on Pearson's Hard/Soft Acid-Base (HSAB) principle. This work was driven by a significant need for high-efficiency sorbents for I-129, a long-lived isotope evolved during irradiated UO2 nuclear fuel reprocessing. These chalcogel compositions are shown to possess an affinity for iodine gas, I2(g), at various concentrations in air and the affinity is attributed to a strong chemical attraction between the chalcogen and I2(g), according to the HSAB principle. The high sorption efficiency is facilitated by the high porosity as well as the exceptionally large surface area of the chalcogels.

Riley, Brian J.; Chun, Jaehun; Ryan, Joseph V.; Matyas, Josef; Li, Xiaohong S.; Matson, Dean W.; Sundaram, S. K.; Strachan, Denis M.; Vienna, John D.

2011-12-22T23:59:59.000Z

148

Characterisation of C-F polymer film formation on the air-bearing surface etched sidewall of fluorine-based plasma interacting with AL2O3-TiC substrate  

Science Conference Proceedings (OSTI)

C-F polymer redeposition is generated on the etched sidewall of the patterned air-bearing surface (ABS). This C-F polymer is a byproduct from fluorine-based plasma using a Surface Technology Systems multiplex-pro air-bearing etch (ABE). The morphology ...

Alonggot Limcharoen, Pichet Limsuwan, Chupong Pakpum, Krisda Siangchaew

2013-01-01T23:59:59.000Z

149

RADIOACTIVE IODINE IN THE TREATMENT OF HYPERTHYROIDISM (EXPERIENCE AT THE TORONTO GENERAL HOSPITAL, 1950-58). PART III. POSSIBLE BIOLOGICAL HAZARDS FROM RADIOACTIVE IODINE THERAPY  

SciTech Connect

A review of 542 hyperthyroid patients treated by I/sup 131/ at the Toronto General Hospital between 1950 and 1955 is presented. This group included 403 patients with diffuse hyperplastic goitre and 139 patients with toxic nodular goitre. The method for assessing the initial dose of I/sup 131/ is described. In general, patients with toxic nodular goitres received much larger doses. Of the diffuse hyperplastic group 72% were cured with one dose, the remainder requiring two or more doses. A greater percentage of the toxic nodular group required only one dose. No cases of complete resistance to 1/sup 131/ therapy were encountered. Permanent hypothyroidism was produced in 16.3% of those so treated, but in 6.5% it was very mild. The incidence of clinical hypothyroidism was much lower in the toxic nodular group than in the diffuse hyperplastic group. There was a continuing incidence of late hypothyroidism, occurring years after therapy; some of these patients had undergone a transient period of hypothyroidism shortly after treatment, then recovered for some years. Factors possibly related to the response to treatment and to the development of hypothyroidism have been analyzed. Recurrent hyperthyroidism after thyroidectomy was associated with a significant increase in the incidence of post-I/sup 131/ hypothyroidism, while pretreatment with artithyroid drugs seemed to reduce radiosensitivity in the diffuse group. No late recurrences of hyperthyroidism were noted. Twenty-one deaths occurred within two years of therapy. In most, there was no obvious relation to therapy, while in none was there a clear-out cause-and-effect relationship to I/sup 131/ therapy. Nevertheless, elderly or very ill patients should be treated only after they have been rendered euthyroid by antithyroid drugs. Fertility has not been affected by I/sup 131/ therapy, but the use of this isotope in pregnancy is contraindicated because of the possible ill effects on the fetas. The possibility of genetic effects appears to be negligible, as judged by the gonadal radiation doses received in I/sup 131/ therapy. The fear of carcinoma of the thyroid likewise appears to be receding if the therapy is utilized only in adults. Leukemia has been reported in 14 instances. However, the statistical import is not clear, since the total number of cases of leukemia and of persons treated by I/sup 131/ is not known. It may be that there is a slight increase in the incidence of leukemia following radioactive treatment, comparable to that possibly induced by certain diagnostic radiological procedures, but this is insufficient to warrant any change in policy regarding the use of I/sup 131/ After consideration of these hypothetical dangers, it is concluded that the use of radioactive iodine is a safe, effective form of therapy for adult, nonpregnant hyperthyroid patients, and is to be preferred to surgical thyroidectomy. 108 references. (auth)

Volpe, R.; Schatz, D.L.; Scott, A.; Peller, J.A.; Vale, J.M.; Ezrin, C.; Johnston, M.W.

1961-01-14T23:59:59.000Z

150

Generation of concentration density maxima of small dispersive coal dust particles in horizontal iodine air filter at air-dust aerosol blow  

E-Print Network (OSTI)

The spatial distributions of the small dispersive coal dust particles with the nano and micro sizes in the granular filtering medium with the cylindrical coal granules in the absorber in the horizontal iodine air filter during its long term operation at the nuclear power plant are researched. It is shown that the concentration density maxima of the small dispersive coal dust particles appear in the granular filtering medium with the cylindrical coal absorbent granules in the horizontal iodine air filter at an action by the air dust aerosol blow. The comparison of the measured aerodynamic resistances of the horizontal and vertical iodine air filters is conducted. The main conclusion is that the magnitude of the aerodynamic resistance of the horizontal iodine air filters is much smaller in comparison with the magnitude of the aerodynamic resistance of the vertical iodine air filters at the same loads of the air dust aerosol volumes. It is explained that the direction of the air dust aerosol blow and the directi...

Neklyudov, I M; Fedorova, L I; Poltinin, P Ya

2013-01-01T23:59:59.000Z

151

Absolute frequency measurement for the emission transitions of molecular iodine in the 982 - 985 nm range  

SciTech Connect

We report high-precision frequency measurements of the separate hyperfine structure (HFS) components of the emission B - X system transitions of {sup 127}I{sub 2} molecules in the 982 - 985 nm range. To resolve the HFS of the emission lines, advantage was taken of the method of three-level laser spectroscopy. The function of exciting radiation was fulfilled by the second harmonic of a cw Nd : YAG laser, and the probe radiation in the 968 - 998 nm range was generated by an external-cavity diode laser. The output Nd : YAG laser frequency was locked to an HFS component of the absorption transition and the probing laser radiation to the emission transition component. When both frequencies were locked to HFS components with a common upper level, the output diode laser frequency was precisely equal to the emission transition frequency. The output frequency of the thus stabilised diode laser was measured with the help of a femtosecond optical frequency synthesiser based on a Ti : sapphire laser. We present the results of the absolute frequency measurements of 20 HFS components belonging to six vibrational - rotational transitions of the B - X system of iodine [R56(32 - 48)a1, P58(32 - 48)a1, P85(33 - 48)a1, R87(33 - 48a1, R88(33 - 48)a10] and all 15 components of the R86(33 - 48) line. The relative measurement uncertainty is equal to 7 Multiplication-Sign 10{sup -10} and is determined by the frequency instability of the diode laser radiation.

Matyugin, Yu A; Ignatovich, S M; Kuznetsov, Sergei A; Nesterenko, M I; Okhapkin, M V; Pivtsov, V S; Skvortsov, Mikhail N; Bagaev, Sergei N [Institute of Laser Physics, Siberian Branch, Russian Academy of Sciences, Novosibirsk (Russian Federation)

2012-03-31T23:59:59.000Z

152

Preliminary results from bench-scale testing of a sulfur-iodine thermochemical water-splitting cycle  

DOE Green Energy (OSTI)

Portions of a bench-scale model of a sulfur-iodine thermochemical water-splitting cycle have been operated at General Atomic Company as part of a comprehensive program to demonstrate the technology for hydrogen production from nonfossil sources. The hydrogen program is funded by the US Department of Energy, the Gas Research Institute, and General Atomic Company. The bench-scale model consists of three subunits which can be operated separately or together and is capable of producing as much as 4 std liters/min (6.7 x 10/sup -5/ m/sup 3//s at standard conditions) of gaseous hydrogen. One subunit (main solution reaction) reacts liquid water, liquid iodine (I/sub 2/) and gaseous sulfur dioxide (SO/sub 2/) to form two separable liquid phases: 50 wt % sulfuric acid (H/sub 2/SO/sub 4/) and a solution of iodine in hydriodic acid (HI/sub x/). Another subunit (H/sub 2/SO/sub 4/ concentration and decomposition) concentrates the H/sub 2/SO/sub 4/ phase to the azeotropic composition, then decomposes it at high temperature over a catalyst to form gaseous SO/sub 2/ and oxygen. The third subunit (HI separation and decomposition) separates the HI from water and I/sub 2/ by extractive distillation with phosphoric acid (H/sub 3/PO/sub 4/) and decomposes the HI in the vapor phase over a catalyst to form I/sub 2/ and product hydrogen. This paper presents the results of on-going parametric studies to determine the operating characteristics, performance, and capacity limitations of major components.

O'Keefe, D.; Allen, C.; Besenbruch, G.; McCorkle, K.; Norman, J.; Sharp, R.

1980-07-01T23:59:59.000Z

153

Kinetics of the processes, plasma parameters, and output characteristics of a UV emitter operating on XeI molecules and iodine molecules and atoms  

SciTech Connect

A kinetic model of the processes occurring in the plasma of a high-power low-pressure gas-discharge lamp is presented, and the output characteristics of the lamp are described. The lamp is excited by a longitudinal glow discharge and emits the I{sub 2}(D Prime -A Prime ) 342-nm and XeI(B-X) 253-nm bands and the 206.2-nm spectral line of atomic iodine. When the emitter operates in a sealed-off mode on the p(He): p(Xe): p(I{sub 2}) = 400: 120: (100-200) Pa mixture, the fractions of the UV radiation power of iodine atoms, exciplex molecules of xenon iodide, and iodine molecules comprise 55, 10, and 35%, respectively. At the optimal partial pressure, the maximum total radiation power of the lamp reaches 37 W, the energy efficiency being about 15%.

Shuaibov, A. K.; Grabovaya, I. A.; Minya, A. I.; Homoki, Z. T. [Uzhgorod National University (Ukraine); Kalyuzhnaya, A. G.; Shchedrin, A. I. [National Academy of Sciences of Ukraine, Institute of Physics (Ukraine)

2011-03-15T23:59:59.000Z

154

Models for calculating the effects of isotopic exchange, radioactive decay, and of recycle in removing iodine from gas and liquid streams  

SciTech Connect

Different decontamination factors for $sup 129$I and $sup 131$I are frequently invoked in environmental impact reports concerned with nuclear fuel recycle. Selected differences, or ratios, have not been justified on the basis of mathematical models or experimental data. A description is given of the origins of these differences in terms of isotopic exchange and material balance equations for the short- and long-lived (or stable) isotopes. The ratios of decontamination factors can be calculated when there is complete attainment of isotopic exchange between gas- or liquid-phase iodine and iodine sorbed by a solid or liquid. If there is no exchange, decontamination factors are isotope- independent unless material recycle occurs within the system. Between these extremes, there can be decontamination factors whose explanation requires experimental determination of the extent of exchange. The model applies to other radioactive isotopes of iodine as well as to other elements with short- and long- lived (or stable) isotopes. (auth)

Davis, W. Jr.

1975-09-01T23:59:59.000Z

155

Scoping calculation for components of the cow-milk dose pathway for evaluating the dose contribution from iodine-131. Hanford Environmental Dose Reconstruction Project: Dose code recovery activities  

Science Conference Proceedings (OSTI)

A series of scoping calculations have been undertaken to evaluate The absolute and relative contribution of different exposure pathways to doses that may have been received by individuals living in the vicinity of the Hanford site. This scoping calculation (Calculation 001) examined the contributions of the various exposure pathways associated with environmental transport and accumulation of iodine-131 in the pasture-cow-milk pathway. Addressed in this calculation were the contributions to thyroid dose of infants and adult from (1) the ingestion by dairy cattle of various feedstuffs (pasturage, silage, alfalfa hay, and grass hay) in four different feeding regimes; (2) ingestion of soil by dairy cattle; (3) ingestion of stared feed on which airborne iodine-131 had been deposited; and (4) inhalation of airborne iodine-131 by dairy cows.

Ikenberry, T.A.; Napier, B.A.

1992-12-01T23:59:59.000Z

156

Commercial Activated Carbon for the Catalytic Production of Hydrogen via the Sulfur-Iodine Thermochemical Water Splitting Cycle  

DOE Green Energy (OSTI)

Eight activated carbon catalysts were examined for their catalytic activity to decompose hydroiodic acid (HI) to produce hydrogen; a key reaction in the sulfur-iodine (S-I) thermochemical water splitting cycle. Activity was examined under a temperature ramp from 473 to 773 K. No statistically significant correlation was found between catalyst sample properties and catalytic activity. Four of the eight samples were examined for one week of continuous operation at 723 K. All samples appeared to be stable over the period of examination.

Daniel M. Ginosar; Lucia M. Petkovic; Kyle C. Burch

2011-07-01T23:59:59.000Z

157

Comparison of silver sorbents for application to radioiodine control at the PUREX process facility modification. [Iodine 129  

SciTech Connect

In continued support of the design of the gaseous radioiodine control system for the PUREX Process Facility Modification (PFM), the Pacific Northwest Laboratory (PNL) conducted laboratory-scale measurements of the performance of four state-of-the-art sorbents for radioiodine in the dissolver offgas (DOG) of a nuclear reprocessing plant. The PFM is a new head-end treatment plant being designed by Westinghouse Hanford Company (WHC) for the PUREX Plant at the Hanford Site. The experiments performed measured the iodine effluent concentration from Norton silver mordenite (NAgZ), Linde silver mordenite (LAgZ), Linde silver faujasite (AgX), and silver nitrate-impregnated silicic acid (AgNO/sub 3/Si) during simulated normal operating conditions in the PFM after three shutdown/startup cycles, and during standby. At normal operating conditions the input gas is expected to have a dew point of 35/degree/C to 40/degree/C and contain 0.1 ..mu..mol I/L, 1 vol% NO, and 1 vol% NO /sub 2/. The sorbent bed would be at 150/degree/C. A shutdown/startup cycle consisted of eliminating iodine and NO/sub x/ from the input gas, cooling the bed to room temperature, stopping gas flow, and restarting the system. During standby conditions the input gas contained no iodine or NO/sub x/, the dew point was at 30/degree/C to 35/degree/C, and the bed temperature remained at 150/degree/C. This experimental study showed that 20 cm beds of NAgZ, LAgZ, and 18 wt% silver AgX could load up to 0.25 mmol I/g sorbent and routinely reduce the iodine concentration in a simulated PFM DOG from 0.1 ..mu..mol I/L to less than the target level of 10/sup /minus/5/ ..mu..mol I/L. In contrast, the AgNO/sub 3/Si unexpectedly failed to achieve this required level of performance, reducing the concentration on a routine basis only to 10/sup /minus/4/ to 10/sup /minus/2/ ..mu..mol I/L. 5 refs., 14 figs., 6 tabs.

Scheele, R.D.; Burger, L.L.; Halko, B.T.

1988-09-01T23:59:59.000Z

158

Low temperature fluorination of Sr{sub 3}Fe{sub 2}O{sub 7-x} with polyvinylidine fluoride: An X-ray powder diffraction and Moessbauer spectroscopy study  

SciTech Connect

Fluorination of the Ruddlesden Popper phase, Sr{sub 3}Fe{sub 2}O{sub 7-x} by heat treatment with polyvinylidine fluoride (PVDF) gives a range of novel oxide fluoride compounds. Fluorination with 1 mol equivalent PVDF leads to a filling of the normal Ruddlesden Popper structure anion sites and a material of composition Sr{sub 3}Fe{sub 2}O{sub 5+x}F{sub 2-x} (x Almost-Equal-To 0.28(4)) which contains both Fe{sup 4+} and Fe{sup 3+}. Increasing the amount of PVDF to 2 mol equivalent leads to an increase in anion content due to filling of half the interstitial sites within the structure, with iron being completely reduced to Fe{sup 3+} leading to a composition Sr{sub 3}Fe{sub 2}O{sub 4}F{sub 4}. An increase in the amount of PVDF to Almost-Equal-To 3 mol equivalent leads to a further increase in unit cell volume, attributed to complete filling of the interstitial sites and a composition Sr{sub 3}Fe{sub 2}O{sub 3}F{sub 6}. {sup 57}Fe Moessbauer spectra in the temperature range 10-300 K demonstrated the complexity of the magnetic interactions in each of the three phases which reflect different local compositions of oxygen and fluorine around the iron ions thus influencing the superexchange pathways. - Graphical abstract: Low temperature (375 Degree-Sign C) fluorination of Sr{sub 3}Fe{sub 2}O{sub 7-x} with poly(vinylidene fluoride) leads to the production of three new Ruddlesden Popper oxide fluorides with progressive filling of the anion sites within the structure. Highlights: Black-Right-Pointing-Pointer The fluorination of Sr{sub 3}Fe{sub 2}O{sub 7-x} using PVDF. Black-Right-Pointing-Pointer The control of the fluorine content with amount of PVDF used. Black-Right-Pointing-Pointer The synthesis of three new Fe based oxide fluorides. Black-Right-Pointing-Pointer The identification of the structures of these oxide fluorides.

Hancock, Cathryn A. [School of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT (United Kingdom); Herranz, Tirma; Marco, Jose F. [Instituto de Quimica Fisica, Consejo Superior de Investigaciones Cientificas, Seranno 119, 28006 Madrid (Spain); Berry, Frank J. [School of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT (United Kingdom); Slater, Peter R., E-mail: p.r.slater@bham.ac.uk [School of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT (United Kingdom)

2012-02-15T23:59:59.000Z

159

Anion retention in soil: Possible application to reduce migration of buried technetium and iodine  

SciTech Connect

This report summarizes a literature review of our present knowledge of the anion exchange properties of a number of soils and minerals, which may potentially be used as anion exchangers to retard migration of such anions as iodide (I{sup {minus}}), iodate (IO{sub 3}{sup {minus}}) and pertechnetate (TcO{sub 4}{sup {minus}}) away from disposal site. The amorphous clays allophane and imogolite, are found to be among the most important soil components capable of developing appreciable amounts of positive charge for anion exchange even at about neutral pH. Decreases in the SiO{sub 2}/Al{sub 2}O{sub 3} ratio and soil pH result in an increase in soil AEC. Allophane and imogolite rich soils have an AEC ranging from 1 to 18 meq/100g at pH about 6. Highly weathered soils dominated by Fe and Al oxides and kaolinite may develop a significant amount of AEC as soil pH falls. The retention of iodine (I) and technetium ({Tc}), by soils is associated with both soil organic matter, and Fe and Al oxides, whereas sorption on layer silicate minerals in negligible. Fe and Al oxides become more important in the retention of anionic I{sup {minus}}, IO{sub 3}{sup {minus}}, and TcO{sub 4}{sup {minus}} as pH falls, since more positive charge is developed on the oxide surfaces. Although few studies, if any, have been conducted on I and {Tc} sorption by soil allophane and imogolite, it is estimated that a surface plough soil (2 million pounds soil per acre) with 5 meq/100g AEC, as is commonly found in andisols, shall retain approximately 5900 kg I and 4500 kg {Tc}. It is conceivable that an anion exchanger such as an andisol could be used to modify the near field environment of a radioactive waste disposal facility. This whole disposal system would then offer similar migration resistance to anions as is normally afforded to cations by usual and normal soils. 93 refs., 10 figs., 7 tabs.

Gu, B.; Schulz, R.K. (California Univ., Berkeley, CA (United States). Dept. of Soil Science)

1991-10-01T23:59:59.000Z

160

Rational synthesis of unidimensional mixed valence solids. Structure oxidation state-charge transport relationships in iodinated nickel and palladium bisbenzoquinonedioximates  

SciTech Connect

A detailed study is presented of crystal structure, stoichiometry, oxidation state, and electron transport in the materials Ni(bqd)/sub 2/, Pd(bqd)/sub 2/, Ni(bqd)/sub 2/I/sub 0/ /sub 018/, Ni(bqd)/sub 2/I/sub 0/ /sub 5/ . S, and Pd(bqd)/sub 2/I/sub 0/ /sub 5/ . S, where bqd = o-benzoquinonedioximato and S = an aromatic solvent. The compound Pd(bqd)/sub 2/I/sub 0/ /sub 50/ . 0.52o-C/sub 6/H/sub 4/Cl/sub 2/ was shown by single-crystal x-ray diffraction to crystallize in the tetragonal space group D/sub 4h//sup 2/-P4/mcc, with four formula units in a cell of dimensions a = 16.048 (7) and c = 6.367 (3) A. The crystal structure consists of stacked Pd(bqd)/sub 2/ units, each staggered by 65/sup 0/ with respect to its nearest neighbors, and disordered chains of iodine atoms extending in the c direction. The Pd--Pd distance is 3.184 (3) A, Pd--N = 1.996 (7) A, and the Pd(bqd)/sub 2/ units are rigorously planar. The predominant form of the iodine present is I/sub 3//sup -/ (..nu../sub fundamental/ 107 cm/sup -1/). Crystallization of Ni(bqd)/sub 2/ from benzene containing traces of iodine produces the new orthorhombic phase Ni(bqd)/sub 2/I/sub 0/ /sub 018/. It crystallizes in the space group D/sub 2h//sup 26/-Ibam with four formula units in a unit cell of dimensions a = 16.438 (2), b = 14.759 (4), and c = 6.360 (2) A. Full-matrix least-squares refinement gave a final value of the conventional R index (on F) of 0.11 for 1026 reflections having F/sub 0//sup 2/ > 3 sigma(F/sub 0//sup 2/). The structure contains rigorously planar Ni(bqd)/sub 2/ units stacked along the c axis with each molecule staggered by 68/sup 0/ with respect to its nearest neighbors. The Ni--Ni distance is 3.180 (2) A and Ni--N = 1.88 (10) A. Single-crystal electrical conductivity measurements (dc and 100-Hz ac) in the stacking direction show an increase in conductivity upon partial oxidation of >10/sup 3/ (Ni) and >10/sup 4/ (Pd). Maximum conductivities at 300 K are determined.

Brown, L.D. (Northwestern Univ., Evanston, IL); Kalina, D.W.; McClure, M.S.; Schultz, S.; Ruby, S.L.; Ibers, J.A.; Kannewurf, C.R.; Marks, T.J.

1979-05-23T23:59:59.000Z

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


161

New oxyfluoride glass with high fluorine content and laser patterning of nonlinear optical BaAlBO{sub 3}F{sub 2} single crystal line  

Science Conference Proceedings (OSTI)

A new oxyfluoride glass of 50BaF{sub 2}-25Al{sub 2}O{sub 3}-25B{sub 2}O{sub 3} (mol. %) with a large fraction of fluorine, i.e., F/(F + O) = 0.4, was prepared using a conventional melt-quenching method in order to synthesize new glass-ceramics containing nonlinear optical oxyfluoride crystals. The refractive index at 632.8 nm and ultra-violet cutoff wavelength of the glass were 1.564 and {approx}200 nm, respectively. Eu{sup 3+} ions in the glass showed a high quantum yield of 88% in the photoluminescence spectrum in the visible region. BaAlBO{sub 3}F{sub 2} crystals (size: 50-100 nm) showing second harmonic generations were formed through the crystallization of the glass. Lines consisting of BaAlBO{sub 3}F{sub 2} crystals were patterned successfully on the glass surface by laser irradiations (Yb:YVO{sub 4} laser with a wavelength of 1080 nm, laser power of 1.1 W, scanning speed of 8 {mu}m/s). High resolution transmission electron microscope observations combined with a focused ion beam technique indicate that BaAlBO{sub 3}F{sub 2} crystals are highly oriented just like a single crystal. The present study proposes that the new oxyfluoride glass and glass-ceramics prepared have a high potential for optical device applications.

Shionozaki, K.; Honma, T.; Komatsu, T. [Department of Materials Science and Technology, Nagaoka University of Technology, 1603-1 Kamitomioka-cho, Nagaoka 940-2188 (Japan)

2012-11-01T23:59:59.000Z

162

Serum thyroxine concentrations following fixed-dose radioactive iodine treatment in hyperthyroid cats: 62 cases (1986-1989)  

SciTech Connect

The medical records of 62 hyperthyroid cats treated with a fixed dose of 4 mCi of radioactive iodine (131I) were reviewed. In 60 cats, serum thyroxine concentrations were determined after treatment, allowing evaluation of treatment success. Eighty-four percent of the cats had normal serum thyroxine concentrations after treatment. Five of the 60 cats (8%) remained hyperthyroxinemic after treatment. Five cats (8%) were hypothyroxinemic when evaluated within 60 days of treatment. Three of these cats had normal serum thyroxine concentrations 6 months after treatment, and none had clinical signs of hypothyroidism. The administration of a fixed dose of 4 mCi of 131I was determined to be an effective treatment for feline hyperthyroidism.

Meric, S.M.; Rubin, S.I. (Univ. of Saskatchewan, Saskatoon (Canada))

1990-09-01T23:59:59.000Z

163

Initial Assessment of Sulfur-Iodine Process Safety Issues and How They May Affect Pilot Plant Design and Operation  

DOE Green Energy (OSTI)

The sulfur-iodine process to make hydrogen by the thermochemical splitting of water is under active development as part of a U.S. Department of Energy program. An integrated lab scale system is currently being designed and built. The next planned stage of development is a pilot plant with a thermal input of about 500 kW, equivalent to about 30,000 standard liters per hour of hydrogen production. The sulfur-iodine process contains a variety of hazards, including temperatures up to 850 ºC and hazardous chemical species including SO2, H2SO4, HI, I2, and of course H2. The siting and design of a pilot plant must consider these and other hazards. This report presents an initial analysis of the hazards that might affect pilot plant design and should be considered in the initial planning. The general hazards that have been identified include reactivity, flammability, toxicity, pressure, electrical hazards, and industrial hazards such as lifting and rotating equipment. Personnel exposure to these hazards could occur during normal operations, which includes not only running the process at the design conditions but also initial inventory loading, heatup, startup, shutdown, and system flushing before equipment maintenance. Because of the complexity and severity of the process, these ancillary operations are expected to be performed frequently. In addition, personnel could be exposed to the hazards during various abnormal situations which could include unplanned phase changes of liquids or solids, leaks of process fluids or cooling water into other process streams, unintentional introducion of foreign species into the process, and unexpected side reactions. Design of a pilot plant will also be affected by various codes and regulations such as the International Building Code, the International Fire Code, various National Fire Protection Association Codes, and the Emergency Planning and Community Right-to-Know Act.

Robert S. Cherry

2006-09-01T23:59:59.000Z

164

Conversion and correction factors for historical measurements of Iodine-131 in Hanford-area vegetation, 1945--1947: Draft. Hanford Environmental Dose Reconstruction Project  

Science Conference Proceedings (OSTI)

This report is a result of the Hanford Environmental Dose Reconstruction (HEDR) Project whose goal is to estimate the radiation dose that individuals could have received from emissions since 1944 at the US Department of Energy`s (DOE) Hanford Site near Richland, Washington. The report describes in detail the reconstructed conversion and correction factors for historical measurements of iodine-131 in Hanford-area vegetation which was collected from the beginning of October 1945 through the end of December 1947.

Mart, E.I.; Denham, D.H.; Thiede, M.E.

1993-05-01T23:59:59.000Z

165

THE CONCENTRATION OF RADIOACTIVE IODINE IN THE THYROID LYMPH, THYROID VENOUS BLOOD, AND PERIPHERAL BLOOD OF PRIMATES  

SciTech Connect

Attempts were made to find out to what extent iodinated compounds are present in lyraph draining from the thyroid gland of the primate, by using baboons, Papio papio, which were injected with 50 to 200 mu C /sup 131/I 2 to 7 days before collection of lymph. Radioiodine was released from the thyroid gland of the baboon into the lymphatic vessels which drain the gland, as well as irto the thyroid venous blood. A high proportion, 90% or more, of the /sup 131/I appeared in the thyroid lymph in organically combined form. The concentration of /sup 131/I in the thyroid lymph was very much higher (10 to 100-fold) than that in the thyroid venous blood or in the peripheral blood. The administration of thyroidstimulating hormone (TSH) rnised the concertration of radioactivity in the thyroid lymph as well as in the thyroid venous blood and these separate effects of TSH appeared to be closely related processes. lt is known that physical or radiation damage to the thyroid gland may lead to the appearance of iodoprotein in the peripheral blood; however, it was possible to exclude the factor of physical daraage by collecting lynaph nt a distance from the gland. To avoid radiation damage, the doses of /sup 131/I used were lower than those generally used in experiments on the release of radioiodine from the thyroid gland. It was shown that if /sup 125/I was used instead of /sup 131/I, the radiation dose rate to the thyroid gland of a small animal can be reducec by a factor of about 25, and a preliminary study, in which /sup 125/I was used in the monkey, suggested that a similar release of radioiodine, in organic form, takes place into the thyroid lymph. It seems unlikely that such a very low radiation dose could damage the thyroid gland. Therefore, it was concluded that the release of iodinated compounds irto the lymphatics of the thyroid is a physiological phenomenon and that it is not due to damage to the gland. (BBB)

Daniel, P.M.; Gale, M.M.; Pratt, O.E.

1963-11-01T23:59:59.000Z

166

Iodine kinetics and dosimetry in the salivary glands during repeated courses of radioiodine therapy for thyroid cancer  

Science Conference Proceedings (OSTI)

Purpose: The present study was conducted to investigate salivary iodine kinetics and dosimetry during repeated courses of radioiodine ({sup 131}I) therapy for differentiated thyroid cancer (DTC). Such data could provide a better understanding of the mechanisms of {sup 131}I induced salivary toxicity and help to develop appropriate methods to reduce this injury. Methods: Seventy-eight consecutive DTC patients (mean age 45 {+-} 17 years, 60%, female) undergoing {sup 131}I therapy for remnant ablation or metastatic tumors were prospectively recruited. Planar quantitative scintigraphy of head-neck images was serially acquired after administration of 2.9-7.4 GBq of {sup 131}I to assess kinetics in the salivary glands of patients. Salivary absorbed doses were calculated based on the schema of Medical Internal Radiation Dosimetry. Results: The maximum uptakes in percentage of administered {sup 131}I activity per kilogram of gland tissue (%/kg) were 12.9% {+-} 6.5%/kg (range, 0.4%-37.3%/kg) and 12.3% {+-} 6.2%/kg (range, 0.4%-35.1%/kg) for the parotid and submandibular glands, respectively. Statistically significant correlations of maximum uptake versus cumulative activity (r = -0.74, P glands; r = -0.71, P glands) and treatment cycle (P gland types) were found. The effective half-lives of {sup 131}I in the parotid and submandibular glands were 9.3 {+-} 3.5 h (range, 1.5-19.8 h) and 8.6 {+-} 3.2 h (range, 0.8-18.0 h), respectively. A statistically significant correlation was observed between effective half-life with cumulative activity (r = 0.37, P glands. The calculated absorbed doses were 0.20 {+-} 0.10 mGy/MBq (range, 0.01-0.92 mGy/MBq) and 0.25 {+-} 0.09 mGy/MBq (range, 0.01-1.52 mGy/MBq) for the parotid and submandibular glands, respectively. The photon contribution to the salivary absorbed dose was minimal in relation to the beta dose contribution. Photon-absorbed dose fractions of total absorbed dose were 4.9% {+-} 1.3% (range, 1.1%-8.7%) and 3.7% {+-} 2.5% (range, 0.8%-7.9%) for the parotid and submandibular glands, respectively. Conclusions: The iodine uptake of salivary glands is continuously reduced during the courses of therapy. The phenomenon of hyper-radiosensitivity may to some extent account for the occurrence of salivary gland hypofunction at very low radiation doses with low dose rates in {sup 131}I therapy. On the other hand, failure to incorporate a nonuniform and preferential uptake by salivary gland ductal cells may result in underestimating the actual dose for the critical tissue. Other methods, including {sup 124}I voxel-based dosimetry, are warranted to further investigate the {sup 131}I-induced salivary gland toxicity.

Liu, B.; Huang, R.; Kuang, A.; Zhao, Z.; Zeng, Y.; Wang, J.; Tian, R. [Department of Nuclear Medicine, West China Hospital, Sichuan University, Chengdu 610041 (China)

2011-10-15T23:59:59.000Z

167

High-Value Fluorine Compounds  

NLE Websites -- All DOE Office Websites (Extended Search)

Compounds Baseline plans call for production of anhydrous or aqueous Hydrogen Fluoride (HF) from the DU hexafluoride conversion plant and subsequent recycle of these...

168

Formation of an SEI on a LiMn(2)O(4) Cathode during Room Temperature Charge-Discharge Cycling Studied by Soft X-Ray Absorption Spectroscopy at the Fluorine K-edge  

DOE Green Energy (OSTI)

The solid electrolyte interface (SEI) formation on the surface of LiMn{sub 2}O{sub 4} electrodes during room temperature charge-discharge cycling was studied using soft X-ray absorption spectroscopy at the Fluorine (F) K-edge. LiMn{sub 2}O{sub 4} electrodes without any binder were prepared by electrostatic spray deposition to eliminate the signal originating from the PVDF binder in the F K-edge X-ray absorption spectra. The F K-edge absorption spectra show that the SEI layer forms at a very early stage of cycling. SEI growth takes place during discharge. In addition, LiF formation is accelerated if the discharge step follows a charge step. The F K-edge absorption spectra suggest that the major component of the SEI is LiF.

Chung, K.Y.; Yang, X.; Yoon, W.-S.; Kim, K.-B.; Cho, B.-W.

2011-11-01T23:59:59.000Z

169

Lessons learned from a review of post-accident sampling systems, high range effluent monitors and high concentration particulate iodine samplers  

Science Conference Proceedings (OSTI)

Post-accident sampling systems (PASS), high range gaseous effluent monitors and sampling systems for particulates and iodine in high concentrations have been reviewed at twenty-one licensee sites in Region I of the US Nuclear Regulatory Commission which includes fifteen BWR's and fourteen PWR's. Although most of the installed PASS met the criteria, the highest operational readiness was found in on-line systems that were also used for routine sampling and analysis. The detectors used in the gaseous effluent monitors included external ion chambers, GM tubes, organic scintillators and Cd-Te solid state crystals. Although all were found acceptable, each had its own inherent limitations in the conversion of detector output to the time varying concentration of a post-accident mixture of noble gases. None of the installed particulate and iodine samplers fully met all of the criteria. Their principal limitations included a lack of documentation showing that they could obtain a representative sample and that many of them would collect of an excessive amount of activity at the design criteria. 10 refs., 4 figs., 5 tabs.

Hull, A.P.; Knox, W.H.; White, J.R.

1987-01-01T23:59:59.000Z

170

Fission product iodine during early Hanford-Site operations: Its production and behavior during fuel processing, off-gas treatment and release to the atmosphere  

Science Conference Proceedings (OSTI)

The Hanford Environmental Dose Reconstruction (HEDR) Project was established to estimate the radiological dose impact that Hanford Site operations may have made on the local and regional population. This impact is estimated by examining operations involving radioactive materials that were conducted at the Hanford Site from the startup of the first reactor in 1944 to the present. HEDR Project work is divided among several technical tasks. One of these tasks, Source Terms, is designed to develop quantitative estimates of all significant emissions of radionuclides by Hanford Site operations since 1944. Radiation doses can be estimated from these emissions by accounting for specific radionuclide transport conditions and population demography. This document provides technical information to assist in the evaluation of iodine releases. 115 refs., 5 figs., 3 tabs.

Burger, L.L.

1991-05-01T23:59:59.000Z

171

Generation of iodine L-shell X-rays under excitation of large CF{sub 3}I clusters by femtosecond laser radiation  

Science Conference Proceedings (OSTI)

The use of clusters of polyatomic molecules with a relatively low ionisation energy ({approx}10 eV) is proposed for the efficient production of X-ray radiation. We have observed for the first time the generation of characteristic X-ray radiation due to L transitions in iodine atoms under the high-intensity femtosecond laser irradiation of molecular CF{sub 3}I clusters, which were a small admixture to Ar carrier gas. The X-ray conversion efficiency amounts to {approx}10{sup -6} (for a yield of {approx}10{sup 7} photons per pulse), which is an order of magnitude higher than the efficiency we obtained in the case of argon clusters under comparable conditions. (letters)

Gordienko, Vyacheslav M; Dzhidzhoev, M S; Zhvaniya, I A; Pribytkov, Andrei V; Trubnikov, Dmitrii N; Fedorov, D O

2012-11-30T23:59:59.000Z

172

Distribution of small dispersive coal dust particles and absorbed radioactive chemical elements in conditions of forced acoustic resonance in iodine air filter at nuclear power plant  

E-Print Network (OSTI)

The physical features of distribution of the small dispersive coal dust particles and the adsorbed radioactive chemical elements and their isotopes in the absorber with the granular filtering medium with the cylindrical coal granules were researched in the case of the intensive air dust aerosol stream flow through the iodine air filter (IAF). It was shown that, at the certain aerodynamic conditions in the IAF, the generation of the acoustic oscillations is possible. It was found that the acoustic oscillations generation results in an appearance of the standing acoustic waves of the air pressure (density) in the IAF. In the case of the intensive blow of the air dust aerosol, it was demonstrated that the standing acoustic waves have some strong influences on both: 1) the dynamics of small dispersive coal dust particles movement and their accumulation in the IAF; 2) the oversaturation of the cylindrical coal granules by the adsorbed radioactive chemical elements and their isotopes in the regions, where the antin...

Ledenyov, Oleg P

2013-01-01T23:59:59.000Z

173

Standard test method for the analysis of refrigerant 114, plus other carbon-containing and fluorine-containing compounds in uranium hexafluoride via fourier-transform infrared (FTIR) spectroscopy  

E-Print Network (OSTI)

1.1 This test method covers determining the concentrations of refrigerant-114, other carbon-containing and fluorine-containing compounds, hydrocarbons, and partially or completely substituted halohydrocarbons that may be impurities in uranium hexafluoride. The two options are outlined for this test method. They are designated as Part A and Part B. 1.1.1 To provide instructions for performing Fourier-Transform Infrared (FTIR) spectroscopic analysis for the possible presence of Refrigerant-114 impurity in a gaseous sample of uranium hexafluoride, collected in a "2S" container or equivalent at room temperature. The all gas procedure applies to the analysis of possible Refrigerant-114 impurity in uranium hexafluoride, and to the gas manifold system used for FTIR applications. The pressure and temperatures must be controlled to maintain a gaseous sample. The concentration units are in mole percent. This is Part A. 1.2 Part B involves a high pressure liquid sample of uranium hexafluoride. This method can be appli...

American Society for Testing and Materials. Philadelphia

2004-01-01T23:59:59.000Z

174

Correlation of radioactive-waste-treatment costs and the environmental impact of waste effluents in the nuclear fuel cycle: conversion of yellow cake to uranium hexafluoride. Part II. The solvent extraction-fluorination process  

Science Conference Proceedings (OSTI)

A cost/benefit study was made to determine the cost and effectiveness of radioactive waste (radwaste) treatment systems for decreasing the release of radioactive materials and chemicals from a model uranium hexafluoride (UF/sub 6/) production plant using the solvent extraction-fluorination process, and to evaluate the radiological impact (dose commitment) of the release materials on the environment. The model plant processes 10,000 metric tons of uranium per year. Base-case waste treatment is the minimum necessary to operate the process. Effluents meet the radiological requirements listed in the Code of Federal Regulations, Title 10, Part 20 (10 CFR 20), Appendix B, Table II, but may not be acceptable chemically at all sites. Additional radwaste treatment techniques are applied to the base-case plant in a series of case studies to decrease the amounts of radioactive materials released and to reduce the amounts of radioactive materials released and to reduce the radiological dose commitment to the population in the surrounding area. The costs for the added waste treatment operations and the corresponding dose committment are correlated with the annual cost for treatment of the radwastes. The status of the radwaste treatment methods used in the case studies is discussed. Much of the technology used in the advanced cases will require development and demonstration, or else is proprietary and unavailable for immediate use. The methodology and assumptions for the radiological doses are found in ORNL-4992.

Sears, M.B.; Etnier, E.L.; Hill, G.S.; Patton, B.D.; Witherspoon, J.P.; Yen, S.N.

1983-03-01T23:59:59.000Z

175

Photoelectron spectroscopy of higher bromine and iodine oxide anions: Electron affinities and electronic structures of BrO2,3 and IO2-4 radicals.  

SciTech Connect

This report details a photoelectron spectroscopy (PES) investigation on electron affinities (EAs) and electronic structures of several atmospherically relevant higher bromine and iodine oxide molecules in the gas phase. PES spectra of BrO{sub 2}{sup -} and IO{sub 2}{sup -} were recorded at 12 K and four photon energies--355 nm/3.496 eV, 266 nm/4.661 eV, 193 nm/6.424 eV, and 157 nm/7.867 eV--while BrO{sub 3}{sup -}, IO{sub 3}{sup -}, and IO{sub 4}{sup -} were studied at 193 and 157 nm only due to their expected high electron binding energies. Spectral features corresponding to transitions from the anion ground state to the ground and excited states of the neutral are unraveled and resolved for each species. For the first time, EAs of these bromine and iodine oxides are experimentally determined (except for IO{sub 2}) to be 2.515 {+-} 0.010 (BrO{sub 2}), 2.575 {+-} 0.010 (IO{sub 2}), 4.60 {+-} 0.05 (BrO{sub 3}), 4.70 {+-} 0.05 (IO{sub 3}), and 6.05 {+-} 0.05 eV (IO{sub 4}). Three low-lying excited states with their respective excitation energies are obtained for BrO{sub 2} [1.69 (A {sup 2}B2), 1.79 (B {sup 2}A{sub 1}), 1.99 eV (C {sup 2}A{sub 2})], BrO{sub 3} [0.7 (A {sup 2}A{sub 2}), 1.6 (B {sup 2}E), 3.1 eV (C {sup 2}E)], and IO{sub 3} [0.60 (A {sup 2}A{sub 2}), 1.20 (B {sup 2}E), {approx}3.0 eV (C {sup 2}E)], whereas six excited states of IO{sub 2} are determined with the respective excitation energies of 1.63 (A {sup 2}B{sub 2}), 1.73 (B {sup 2}A{sub 1}), 1.83 (C {sup 2}A{sub 2}), 4.23 (D {sup 2}A{sub 1}), 4.63 (E {sup 2}B{sub 2}), and 5.23 eV (F {sup 2}B{sub 1}). Periodate possesses a very high electron binding energy. Only one excited state feature with 0.95 eV excitation energy is shown in the 157 nm spectrum. The obtained EAs and low-lying excited state information are compared with available theoretical calculations and discussed with their atmospheric implications.

Wen, Hui; Hou, Gaolei; Huang, Wei; Govind, Niranjan; Wang, Xue B.

2011-11-14T23:59:59.000Z

176

Distribution of small dispersive coal dust particles and absorbed radioactive chemical elements in conditions of forced acoustic resonance in iodine air filter at nuclear power plant  

E-Print Network (OSTI)

The physical features of distribution of the small dispersive coal dust particles and the adsorbed radioactive chemical elements and their isotopes in the absorber with the granular filtering medium with the cylindrical coal granules were researched in the case of the intensive air dust aerosol stream flow through the iodine air filter (IAF). It was shown that, at the certain aerodynamic conditions in the IAF, the generation of the acoustic oscillations is possible. It was found that the acoustic oscillations generation results in an appearance of the standing acoustic waves of the air pressure (density) in the IAF. In the case of the intensive blow of the air dust aerosol, it was demonstrated that the standing acoustic waves have some strong influences on both: 1) the dynamics of small dispersive coal dust particles movement and their accumulation in the IAF; 2) the oversaturation of the cylindrical coal granules by the adsorbed radioactive chemical elements and their isotopes in the regions, where the antinodes of the acoustic waves are positioned. Finally, we completed the comparative analysis of the theoretical calculations with the experimental results, obtained for the cases of: 1) the experimental aerodynamic modeling of physical processes of the absorbed radioactive chemical elements and their isotopes distribution in the IAF; and 2) the gamma-activation spectroscopy analysis of the absorbed radioactive chemical elements and their isotopes distribution in the IAF. We made the innovative propositions on the necessary technical modifications with the purpose to improve the IAF technical characteristics and increase its operational time at the nuclear power plant (NPP), going from the completed precise characterization of the IAF parameters at the long term operation.

Oleg P. Ledenyov; Ivan M. Neklyudov

2013-06-14T23:59:59.000Z

177

FLUORINE PROCESS FOR SEPARATION OF MATERIALS  

DOE Patents (OSTI)

A process is described for separating plutoniunn from neutron-irradiated uranium, which consists of reacting the irradiated uranium mass with HF to form the tetrafluorides of U, Pu, and Np, and then reacting this mixture of tetrafluorides with fiuorine at temperature between 140 and 315 d C. This causes volatile hexafluorides of U and Np to form while at the temperature employed the Pu tetrafluoride is unaffected and remains as a residue.

Seaborg, G.T.; Brown, H.S.

1958-05-01T23:59:59.000Z

178

Growth, Characterization, Modeling and Device Applications of Semiconductor Nanowire Networks  

E-Print Network (OSTI)

from aluminum oxide coated indium phos- phide nanowirespectroscopy of aluminum oxide coated indium phos- phidealuminum oxide coated (top) and uncoated (bottom) indium

Lohn, Andrew John

2012-01-01T23:59:59.000Z

179

Oak Ridge Reservation Volume 3. Records relating to RaLa, iodine-131, and cesium-137 at the Oak Ridge National Laboratory and the Oak Ridge Operations Office: A guide to record series of the Department of Energy and its contractors  

SciTech Connect

The purpose of this guide is to describe each of the documents and record series pertaining to the production, release, and disposal of radioactive barium-lanthanum (RaLa), iodine-131, and cesium-137 at the Department of Energy`s (DOE) Oak Ridge National Laboratory (ORNL) in Oak Ridge, Tennessee. History Associates Incorporated (HAI) prepared this guide as part of DOE`s Epidemiologic Records Inventory Project, which seeks to verify and conduct inventories of epidemiologic and health-related records at various DOE and DOE contractor sites. This introduction briefly describes the Epidemiologic Records Inventory Project and HAI`s role. It provides information on the history of the DOE-Oak Ridge Reservation (ORR), particularly ORNL. Specific attention is given to the production of RaLa and the fission products iodine-131 and cesium-137. This introduction also describes the methodologies HAI used in the selection and inventorying of documents and record series pertaining to RaLa, iodine-131, and cesium-137, and in the production of this guide. Concluding paragraphs describe the arrangement of the record series, explain the information contained in the record series descriptions, and indicate restrictions on access to the records.

NONE

1995-03-21T23:59:59.000Z

180

Experimental investigation of the chemistry of excited states of rare gases. Third quarterly progress report, April 15, 1979-July 15, 1979  

SciTech Connect

Photosensitized studies of Xe(/sup 3/P/sub 1/) and Kr(/sup 3/P/sub 1/) reactions with fluorine, chlorine, bromine, and iodine donors have been very productive. Work on the laser excitation methods for generating selected states of the rare gas atoms lying above the np/sup 5/,n + 1s set of levels continued.

Setser, D.W.

1979-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


181

A permanent breast seed implant as partial breast radiation therapy for early-stage patients: A comparison of palladium-103 and iodine-125 isotopes based on radiation safety considerations  

Science Conference Proceedings (OSTI)

Purpose: A permanent breast seed implant (PBSI) technique has been developed as a new form of partial adjuvant radiation therapy for early-stage breast cancer. This study compares iodine-125 ({sup 125}I) and palladium-103 ({sup 103}Pd) isotopes by examining the exposure and effective dose (ED) to a patient's partner.Methods and Materials: A low-energy survey meter was used to measure exposure rates as a function of bolus thickness placed over {sup 103}Pd or {sup 125}I seeds. A general mathematical expression for the initial exposure rate at 1 m (x{sub o,1m}) from the skin surface as a function of the implant size, R, and the distance between the skin surface and the implant, d, was derived. Also, a second general equation is proposed to calculate the ED to the patient's partner.Results: The initial exposure rate at 1 meter and the ED are calculated as follows: x{sub o,1m} = (3{alpha})/2R{sup 3}{center_dot}{beta}{sup 3} [e{sup -{beta}}{sup (2R+d)}({beta}R + 1) + e{sup -{beta}}{sup {center_dot}}{sup d}({beta}R - 1)], and ED = aR{sup b} {center_dot} [e{sup -c(2R+d)} {center_dot} (cR + 1) + e{sup -cd} -bar (cR - 1)]. For {sup 125}I, the parameters are: {alpha} = 0.154409, {beta} = 0.388460, a = 197, b = -0.95, and c = 0.38846. For {sup 103}Pd, they are: {alpha} = 0.06877, {beta} = 0.421098, a = 18.6, b -0.78, and c = 0.421098. For implant diameters varying from 2 to 6 cm and skin-to-implant distances varying from 0.7 to 4 cm, the ED is consistently below 2.6 mSv using the {sup 103}Pd isotope, but more than 5 mSv in many instances and possibly up to 20 mSv using {sup 125}I.Conclusions: PBSI using {sup 103}Pd seeds appears safe because the patient's partner ED is consistently below 5 mSv. The{sup 125}I isotope is not recommended for PBSI.

Keller, Brian [Department of Medical Physics, Sunnybrook and Women's Health Sciences Centre, Toronto, Ontario (Canada); Sankreacha, Raxa [Department of Medical Physics, Sunnybrook and Women's Health Sciences Centre, Toronto, Ontario (Canada); Rakovitch, Eileen [Department of Radiation Oncology, Sunnybrook and Women's Health Sciences Centre, Toronto, Ontario (Canada); O'Brien, Peter [Department of Medical Physics, Sunnybrook and Women's Health Sciences Centre, Toronto, Ontario (Canada); Pignol, Jean-Philippe [Department of Radiation Oncology, Sunnybrook and Women's Health Sciences Centre, Toronto, Ontario (Canada)]. E-mail: Jean-Philippe.Pignol@sw.ca

2005-06-01T23:59:59.000Z

182

The Atmospheric Chemistry of Iodine Monoxide  

Science Conference Proceedings (OSTI)

... of I, and C1, or by reaction of 0 with a mixture of IC1 and CIO,. ... Stein, SE; Rukkers, JM; Brown, RM NIST Structures & Properties Database; ver. ...

2011-10-18T23:59:59.000Z

183

It's Elemental - Isotopes of the Element Iodine  

NLE Websites -- All DOE Office Websites (Extended Search)

Available No Data Available No Data Available 108 36 milliseconds Alpha Decay 91.00% Electron Capture 9.00% Proton Emission < 1.00% 109 93.5 microseconds Proton Emission 99.99%...

184

Single and double stereoselective fluorination of (E)-allylsilanes  

E-Print Network (OSTI)

solution of ethyl-(E)-2-methyl-3-trimethylsilylhex-4-enoate (2.052g, 9.0mmol) in THF (4.5ml) was added via a syringe. The temperature was gradually raised to -40°C over a period of 2hrs. After which time iodomethane (0.735ml, 11.8mmol, 1.3 eq) was added... was added n-BuLi (2.5M, 2.9ml, 7.2mmol, 1.2eq.), the reaction was allowed to stir for 30 min. The solution was cooled to -78°C and a solution of ethyl-(E)-3-trimethylsilylhex-4-enoate (1.28g, 6.0mmol) in THF (5ml) was added via a syringe. The light yellow...

Sawicki, Marcin; Kwok, Angela; Tredwell, Matthew; Gouverneur, Veronique

2007-10-25T23:59:59.000Z

185

Influence of the Slag Composition on the Fluorine Absorption in ...  

Science Conference Proceedings (OSTI)

Author(s), Peter Spiess, Bernd Friedrich. On-Site Speaker (Planned), Peter Spiess. Abstract Scope, Because of the oxidation resistance of gamme-TiAl-

186

Mark L. Robin Great Lakes Chemical Corporation Fluorine ...  

Science Conference Proceedings (OSTI)

... Results for the FM-100/air/propane and FM-lOO/air/i-butane systems are shown in Figures 3 and 4 , respectively. ... n-heptane n-butane methanol ...

2011-09-27T23:59:59.000Z

187

Experimental Research on the Absorption of Fluorine in Gamma ...  

Science Conference Proceedings (OSTI)

Evolution of ESR Technology and Equipment for Long Hollow Ingots Manufacture ... Phosphorus Partitioning During EAF Refining of DRI Based Steel.

188

Arylene-fluorinated-sulfonimide ionomers and membranes for fuel cells  

Science Conference Proceedings (OSTI)

The preparation of aromatic sulfonimide polymers useful as membranes in electrochemical cells is described.

Teasley, Mark F. (Landenberg, PA)

2011-11-15T23:59:59.000Z

189

Low Temperature Reduction of Alumina Using Fluorine Containing Ionic Liquids  

SciTech Connect

The major objective of the project is to establish the feasibility of using specific ionic liquids capable of sustaining aluminum electrolysis near room temperature at laboratory and batch recirculation scales. It will explore new technologies for aluminum and other valuable metal extraction and process methods. The new technology will overcome many of the limitations associated with high temperatures processes such as high energy consumption and corrosion attack. Furthermore, ionic liquids are non-toxic and could be recycled after purification, thus minimizing extraction reagent losses and environmental pollutant emissions. Ionic liquids are mixture of inorganic and organic salts which are liquid at room temperature and have wide operational temperature range. During the last several years, they were emerging as novel electrolytes for extracting and refining of aluminum metals and/or alloys, which are otherwise impossible using aqueous media. The superior high temperature characteristics and high solvating capabilities of ionic liquids provide a unique solution to high temperature organic solvent problems associated with device internal pressure build-up, corrosion, and thermal stability. However their applications have not yet been fully implemented due to the insufficient understanding of the electrochemical mechanisms involved in processing of aluminum with ionic liquids. Laboratory aluminum electrodeposition in ionic liquids has been investigated in chloride and bis (trifluoromethylsulfonyl) imide based ionic liquids. The electrowinning process yielded current density in the range of 200-500 A/m2, and current efficiency of about 90%. The results indicated that high purity aluminum (>99.99%) can be obtained as cathodic deposits. Cyclic voltammetry and chronoamperometry studies have shown that initial stages of aluminum electrodeposition in ionic liquid electrolyte at 30°C was found to be quasi-reversible, with the charge transfer coefficient (0.40). Nucleation phenomena involved in aluminum deposition on copper in AlCl3-BMIMCl electrolyte was found to be instantaneous followed by diffusion controlled three-dimensional growth of nuclei. Diffusion coefficient (Do) of the electroactive species Al2Cl7¯ ion was in the range from 6.5 to 3.9×10–7 cm2?s–1 at a temperature of 30°C. Relatively little research efforts have been made toward the fundamental understanding and modeling of the species transport and transformation information involved in ionic liquid mixtures, which eventually could lead to quantification of electrochemical properties. Except that experimental work in this aspect usually is time consuming and expensive, certain characteristics of ionic liquids also made barriers for such analyses. Low vapor pressure and high viscosity make them not suitable for atomic absorption spectroscopic measurement. In addition, aluminum electrodeposition in ionic liquid electrolytes are considered to be governed by multi-component mass, heat and charge transport in laminar and turbulent flows that are often multi-phase due to the gas evolution at the electrodes. The kinetics of the electrochemical reactions is in general complex. Furthermore, the mass transfer boundary layer is about one order of magnitude smaller than the thermal and hydrodynamic boundary layer (Re=10,000). Other phenomena that frequently occur are side reactions and temperature or concentration driven natural convection. As a result of this complexity, quantitative knowledge of the local parameters (current densities, ion concentrations, electrical potential, temperature, etc.) is very difficult to obtain. This situation is a serious obstacle for improving the quality of products, efficiency of manufacturing and energy consumption. The gap between laboratory/batch scale processing with global process control and nanoscale deposit surface and materials specifications needs to be bridged. A breakthrough can only be realized if on each scale the occurring phenomena are understood and quantified. Multiscale numerical modeling nevertheless can help t

Dr. R. G. Reddy

2007-09-01T23:59:59.000Z

190

Fluorine Abatement: Non-thermal Plasma for the Destruction ...  

Pacific Northwest National Laboratory Skip to Main Content U.S. Department of Energy. Search PNNL. PNNL Home; About; Research; Publications; Jobs; ...

191

Fluorine Induced Twinned Crystalline SnO2 Thin Films  

Science Conference Proceedings (OSTI)

Accelerated Light Induced Degradation, ALID, for Monitoring of Defects in PV Silicon ... Silicon Solar Cells Evaluated by LBIC and Equivalent Circuit Model.

192

790 Series RIE (Fluorine-Metal Etch) Plasma Processing ...  

Science Conference Proceedings (OSTI)

... 5. Turn the chiller for RIE which is located at the back of pumps on the extreme right ON by turning the ON-OFF Switch On and then pressing the ...

2006-07-31T23:59:59.000Z

193

Unaxis 790 Series RIE Metal Fluorine Plasma Processing ...  

Science Conference Proceedings (OSTI)

... These control setting phases are performed in the following steps: • System initialization • Process Programming • Process Operation System Power ...

2013-10-26T23:59:59.000Z

194

Zevenhoven & Kilpinen Halogens, dioxins/furans 17.6.2001 7-1 Chapter 7 Halogens,  

E-Print Network (OSTI)

and important halogen is chlorine. In nature, fluorine is mainly found in minerals such as CaF2 and Na2AlF6 for the other halogens - see Table 7.1. Natural gas and oil-derived fuels contain very small amounts of halogens Natural gas - * Iodine 0.5 - 1.5 mg/kg In biomasses, especially straw, the presence of halogens is largely

Zevenhoven, Ron

195

Simulation of the sulphur iodine thermochemical cycle / Bothwell Nyoni.  

E-Print Network (OSTI)

??The demand for energy is increasing throughout the world, and fossil fuel resources are diminishing. At the same time, the use of fossil fuels is… (more)

Nyoni, Bothwell

2011-01-01T23:59:59.000Z

196

Technetium and Iodine Separations in the UREX Process.  

Science Conference Proceedings (OSTI)

The Accelerator Transmutation of Waste (ATW) program is being developed to determine the feasibility of separatin and transmutating the transactinides (Pu-Cm) and long-lived fission product (99Tc and 'I) from spent light water reactor (LWR) fuel. This approach would help with the disposal of spent commercial fuel. In addition, since the residual waste after ATW treatment will have much lower levels of long-lived species, this process may improve the performance and acceptability of long-term geologic disposal of nuclear waste. A roadmap for the Accelerator Transmutation of Waste (ATW) was submitted to Congress in 1999.' This document gave an overall view of the ATW concept and program. A subsequent document prepared by the Technical Working Group for ATW Separations Technologies and Waste Forms issued a second roadmap that dealt more specifically with the radionuclide separations and waste disposal needs for the ATW program.' This latter document discusses the UREX (Uranium Extraction) process. The latest iteration of the UREX flowsheet is shown in Figure le3T his flowsheet anticipates the co-extraction of technetium with uranium from dissolved LWR fuel by tributylphosphate (TBP) and their subsequent sequential bwk-extraction from the TBP stream.

Schroeder, N. C. (Norman C.); Attrep, Moses; Marrero, T. (Thomas)

2001-01-01T23:59:59.000Z

197

Adsorption of of Radioactive Iodine from Used Nuclear Fuel ...  

Science Conference Proceedings (OSTI)

... of Fluidized Bed Steam Reforming (FBSR) with Hanford Low Activity Wastes ... Level Waste at the Defense Waste Processing Facility through Sludge Batch 7b.

198

Migration of Iodine Solidified in Ettringite into Compacted Bentonite  

Science Conference Proceedings (OSTI)

... of Fluidized Bed Steam Reforming (FBSR) with Hanford Low Activity Wastes ... Level Waste at the Defense Waste Processing Facility through Sludge Batch 7b.

199

Acta Crystallographica Section D Optimum solubility (OS) screening ...  

methane]; TCEP, tris(2-carboxyethyl) phos-phine. 2. Introduction Advances in X-ray crystallography have provided three-dimensional structures of

200

Method for the simultaneous preparation of radon-211, xenon-125, xenon-123, astatine-211, iodine-125 and iodine-123  

DOE Patents (OSTI)

The invention relates to a practical method for commercially producing radiopharmaceutical activities and, more particularly, relates to a method for the preparation of about equal amount of Radon-211 (/sup 211/Rn) and Xenon-125 (/sup 125/Xe) including a one-step chemical procedure following an irradiation procedure in which a selected target of Thorium (/sup 232/Th) or Uranium (/sup 238/U) is irradiated. The disclosed method is also effective for the preparation in a one-step chemical procedure of substantially equal amounts of high purity /sup 123/I and /sup 211/At. In one preferred arrangement of the invention almost equal quantities of /sup 211/Rn and /sup 125/Xe are prepared using a onestep chemical procedure in which a suitably irradiated fertile target material, such as thorium-232 or uranium-238, is treated to extract those radionuclides from it. In the same one-step chemical procedure about equal quantities of /sup 211/At and /sup 123/I are prepared and stored for subsequent use. In a modified arrangement of the method of the invention, it is practiced to separate and store about equal amounts of only /sup 211/Rn and /sup 125/Xe, while preventing the extraction or storage of the radionuclides /sup 211/At and /sup 123/I.

Mirzadeh, S.; Lambrecht, R.M.

1985-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


201

Fluorination of "brick and mortar" soft-templated graphitic ordered mesoporous carbons for high  

E-Print Network (OSTI)

compared to standard OMCs, making these ideal candidates for supercapacitor and rechargeable Li-ion battery

Geohegan, David B.

202

Chlorine, Fluorine and Water in the Stratosphere: Chemistry, Transport and Trends  

E-Print Network (OSTI)

in their effects on the global energy balance [Bernath et al., 2005]. The primary instrument onboard the ACE. The ACE satellite is powered by solar energy and is always oriented with its solar panel in the direction to radiate excess energy and cool the FTS detectors. During an occultation, the ACE instruments observe

Nassar, Ray

203

Plasma-assisted CVD of fluorinated, hydrogenated amorphous silicon. Final report  

DOE Green Energy (OSTI)

During the past year, three novel large-area (100 cm/sup 2/) a-Si:H solar cells were developed with the following configurations: inverted NIP/SS cells with an improved red response; inverted a-Si:H/a-B:H heterojunction cells with high V/sub oc/; and NIP/metal cells with a CVD P-layer grown pyrolytically from silane and diborane. Initial experiments were performed using disilane as the deposition gas for the intrinsic layer in both NIP/SS and PIN/SS structures. Coatings of In/sub 2/O/sub 3/, using a technique developed by Dr. Ovadyahu, were applied to NIP/SS cells in order to evaluate its potential as a conductive coating in practical amorphous silicon solar cells.

Coleman, J.H.; Hammes, J.P.; Wiesmann, H.J.

1981-01-01T23:59:59.000Z

204

Fluorinated Graphene as a Low-k Dielectric for Graphene Devices  

Science Conference Proceedings (OSTI)

About this Abstract. Meeting, 2013 TMS Annual Meeting & Exhibition. Symposium , 2013 Functional Nanomaterials: Synthesis, Properties and Applications.

205

Study on a River Containing Fluorine and the Pollution Control Method  

Science Conference Proceedings (OSTI)

These plants emitted high fluoride wastewater, and need to strengthen the fluoride ... A Kinetics Study on the Hydrometallurgical Recovery of Vanadium from LD ... the Chemical Changes and Surface Properties of Carbonated Waste Cement ... Heat Treatment of Black Dross for the Production of a Value Added Material - A ...

206

Synthesis and study of ligands for Pd-catalyzed C-O and C-N coupling  

E-Print Network (OSTI)

A new ligand, AdBrettPhos, was synthesized and its use, along with tBuBrettPhos, in C-O coupling reactions at low temperatures was investigated. Using Pd catalysts containing these ligands, electron-neutral aryl bromides ...

Davis, Nicole R

2009-01-01T23:59:59.000Z

207

NA Standards | Refinement Parameters | X-PLOR parameter file  

NLE Websites -- All DOE Office Websites (Extended Search)

Bases 18.75% Sugar 56.6% Phos 154.8% remark K scale*(kTsigma**2), scalesBase 0.1875, Sugar 0.566, Phos 1.548 removed references to CA, CF, CS, MG, NH3, OS (ATB 123094) ...

208

Technology Commercialization and Partnerships | BSA 03-01 ...  

Fluorinated precursors for superconducting ceramics typically increase the critical current in the superconductors they produce. Here the fluorinated ...

209

Plasma-assisted CVD of fluorinated, hydrogenated amorphous silicon. Final technical report, September 15, 1979-September 15, 1980  

DOE Green Energy (OSTI)

During the past year, approximately 300 large-area (400 cm/sup 2/) PIN hydrogenated amorphous silicon (a-Si:H) solar cells were fabricated and tested. a-Si:H PIN cells which were plasma deposited at 200/sup 0/ to 350/sup 0/ were found to have high internal currents (13mA/cm/sup 2/), whereas those which were deposited by CVD at 500/sup 0/ to 650/sup 0/C had low internal currents. When corrected for optical losses in the top electrode, the internal quantum efficiency vs wavelength for the PIN cells indicated a peak value above 80% at about 525nm, which decreased monotonically to zero at about 725 nm. When the published values of RCA and EXXON were corrected similarly for optical loss, nearly identical values of internal quantum efficiencies were found. Calculations based on a model proposed by Cody et al of EXXON indicated that the depletion width was less than 0.4 microns for all PIN cells, thereby limiting junction efficiency in the red portion of the solar spectrum since the 1/e photon range exceeds this value. A novel inverted NIP cell was tested and found to have its maximum quantum response shifted to 625 nm. Also, an amorphous boron (a-B) layer deposited on a-Si:H to form a PIN heterojunction improved blue response and Voc. A combination of the red-responsive cells and the a-B heterojunction cells could raise efficiency to 8%.

Coleman, J. H.; Hammes, J. P.; Wiesmann, H. J.

1980-01-01T23:59:59.000Z

210

Method of Determining the Extent to which a Nickel Structure has been Attached by a Fluorine-Containing Gas  

DOE Patents (OSTI)

The method of determining the extent to which a nickel structure has been attacked by a halogen containing gas to which it has been exposed which comprises preparing a quantity of water substantially free from dissolved oxygen, passing ammonia gas through a cuprammonium solution to produce ammonia substantially free from oxygen, dissolving said oxygen-free ammonia in said water to produce a saturated aqueous ammonia solution free from uncombined oxygen, treating at least a portion of said nickel structure of predetermined weight with said solution to dissolve nickel compounds from the surface of said structure without dissolving an appreciable amount of said nickel and analyzing the resulting solution to determine the quantity of said nickel compounds that was associated with said said portion of said structure to determine the proportion of combined nickel in said nickel structure.

Brusie, James P.

2004-07-13T23:59:59.000Z

211

Potatoes in the Home Garden  

E-Print Network (OSTI)

after being turned under. A compost made of a grass/legumeand phos- phorous. The compost mix should be applied at and15” of soil). While the compost needs to be stable, potatoes

Martin, Orin

2008-01-01T23:59:59.000Z

212

NIDC: Online Catalog of Isotope Products | Product Search  

NLE Websites -- All DOE Office Websites (Extended Search)

Product Search Product Search Step 1 - Enter your search criteria below. Element Name Actinium Aluminum Americium Antimony Argon Arsenic Astatine Barium Berkelium Beryllium Bismuth Bohrium Boron Bromine Cadmium Caesium Calcium Californium Carbon Cerium Chlorine Chromium Cobalt Copernicium Copper Curium Darmstadtium Dubnium Dysprosium Einsteinium Erbium Europium Fermium Fluorine Francium Gadolinium Gallium Germanium Gold Hafnium Hassium Helium Holmium Hydrogen Indium Iodine Iridium Iron Krypton Lanthanum Lawrencium Lead Lithium Lutetium Magnesium Manganese Meitnerium Mendelevium Mercury Molybdenum Neodymium Neon Neptunium Nickel Niobium Nitrogen Nobelium Osmium Oxygen Palladium Phosphorus Platinum Plutonium Polonium Potassium Praseodymium Promethium Protactinium Radium Radon Rhenium Rhodium Roentgenium Rubidium Ruthenium Rutherfordium Samarium Scandium Seaborgium Selenium Silicon Silver Sodium Strontium Sulfur Tantalum Technetium Tellurium Terbium Thallium Thorium Thulium Tin Titanium Tungsten Ununhexium Ununoctium Ununpentium Ununquadium Ununseptium Ununtrium Uranium Vanadium Xenon Ytterbium Yttrium Zinc Zirconium

213

NIDC: Online Catalog of Isotope Products | Request a New Product  

NLE Websites -- All DOE Office Websites (Extended Search)

Request a New Product Request a New Product Step 1 - Enter the new product's criteria below. Element Name Actinium Aluminum Americium Antimony Argon Arsenic Astatine Barium Berkelium Beryllium Bismuth Bohrium Boron Bromine Cadmium Caesium Calcium Californium Carbon Cerium Chlorine Chromium Cobalt Copernicium Copper Curium Darmstadtium Dubnium Dysprosium Einsteinium Erbium Europium Fermium Fluorine Francium Gadolinium Gallium Germanium Gold Hafnium Hassium Helium Holmium Hydrogen Indium Iodine Iridium Iron Krypton Lanthanum Lawrencium Lead Lithium Lutetium Magnesium Manganese Meitnerium Mendelevium Mercury Molybdenum Neodymium Neon Neptunium Nickel Niobium Nitrogen Nobelium Osmium Oxygen Palladium Phosphorus Platinum Plutonium Polonium Potassium Praseodymium Promethium Protactinium Radium Radon Rhenium Rhodium Roentgenium Rubidium Ruthenium Rutherfordium Samarium Scandium Seaborgium Selenium Silicon Silver Sodium Strontium Sulfur Tantalum Technetium Tellurium Terbium Thallium Thorium Thulium Tin Titanium Tungsten Ununhexium Ununoctium Ununpentium Ununquadium Ununseptium Ununtrium Uranium Vanadium Xenon Ytterbium Yttrium Zinc Zirconium

214

Method oil shale pollutant sorption/NO.sub.x reburning multi-pollutant control  

DOE Patents (OSTI)

A method of decreasing pollutants produced in a combustion process. The method comprises combusting coal in a combustion chamber to produce at least one pollutant selected from the group consisting of a nitrogen-containing pollutant, sulfuric acid, sulfur trioxide, carbonyl sulfide, carbon disulfide, chlorine, hydroiodic acid, iodine, hydrofluoric acid, fluorine, hydrobromic acid, bromine, phosphoric acid, phosphorous pentaoxide, elemental mercury, and mercuric chloride. Oil shale particles are introduced into the combustion chamber and are combusted to produce sorbent particulates and a reductant. The at least one pollutant is contacted with at least one of the sorbent particulates and the reductant to decrease an amount of the at least one pollutant in the combustion chamber. The reductant may chemically reduce the at least one pollutant to a benign species. The sorbent particulates may adsorb or absorb the at least one pollutant. A combustion chamber that produces decreased pollutants in a combustion process is also disclosed.

Boardman, Richard D. (Idaho Falls, ID); Carrington, Robert A. (Idaho Falls, ID)

2008-06-10T23:59:59.000Z

215

Investigations into the Nature of Halogen Bonding Including Symmetry Adapted Perturbation Theory Analyses  

Science Conference Proceedings (OSTI)

In recent years it has been recognized that, because of their unique properties, halogen bonds have tremendous potential in the development of new pharmaceutical compounds and materials. In this study we investigate the phenomenon of halogen bonding by carrying out ab initio calculations on the halomethane-formaldehyde complexes as well as the fluorine substituted FnH?-nCX---OCH? dimers, where the halogen bonding halogens (X) are chlorine, bromine, and iodine. Coupled cluster (CCSD(T)/aug-cc-pVTZ) calculations indicate that the binding energies for these type of interactions lie in the range between -1.05 kcal/mol (H?CCl---OCH?) and -3.72 kcal/mol (F?CI---OCH?). One of the most important findings in this study is that, according to symmetry adapted perturbation theory (SAPT) analyses, halogen bonds are largely dependent on both electrostatic and dispersion type interactions. As the halogen atom involved in halogen bonding becomes larger the interaction strength for this type of interaction also gets larger and, interestingly, more electrostatic (and less dispersive) in character. Halogen bonding interactions also become stronger and more electrostatic upon substitution of (the very electronegative) fluorines onto the halomethane molecule.

Riley, Kevin E.; Hobza, Pavel

2008-01-12T23:59:59.000Z

216

In or Out: Setting a Trap for Radioactive Iodine | Advanced Photon...  

NLE Websites -- All DOE Office Websites (Extended Search)

Moment in a Split Picosecond Unpeeling Atoms and Molecules from the Inside Out Butterfly Wing Yields Clues to Light-Altering Structures Squeezing Information from Materials under...

217

Prostate-Specific Antigen Bounce After Permanent Iodine-125 Prostate Brachytherapy-An Australian Analysis  

SciTech Connect

Purpose: To report on prostate-specific antigen (PSA) 'bounces' after {sup 125}I prostate brachytherapy to review the relationship to biochemical control and correlate both clinical and dosimetric variables. Methods and Materials: We analyzed 194 hormone-naive patients with a follow-up of {>=}3 years. Four bounce definitions were applied: an increase of {>=}0.2 ng/mL (definition I), {>=}0.4 ng/mL (definition II), {>=}15% (definition III), and {>=}35% (definition IV) of a previous value with spontaneous return to the prebounce level or lower. Results: Using definition I, II, III, and IV, a bounce was detected in 50%, 34%, 11%, and 9% of patients, respectively. The median time to onset was 14-16 months, the duration was 12-21.5 months, and the magnitude of the increase was 0.5-2 ng/mL. A magnitude of >2 ng/mL, fulfilling the criteria for biochemical failure (BF) according to the American Society for Therapeutic Radiology and Oncology Phoenix definition, was detected in 11.3%, 16.9%, 47.6%, and 50% using definitions I, II, III, and IV, respectively; 11 patients (5.7%) had true BF. The PSA bounces occurred earlier than BF (p < 0.001). The prediction of BF remains controversial and is probably unrelated to biochemical control. The only statistically significant factor predictive of a PSA bounce was younger age (definitions I and II). Conclusion: PSA bounces are common after brachytherapy. All definitions resulted in a high number of false-positive calls for BF during the first 2 years. The definition of an increase of {>=}0.2 ng/mL should be preferred because of the lowest number of false-positive results for BF. Patients experiencing a PSA bounce during the first 2 years after brachytherapy should undergo surveillance every 3-6 months. Additional investigations are recommended for elevated postimplant PSA levels that have not corrected by 3 years of follow-up.

Zwahlen, Daniel R.; Smith, Ryan [Department of Radiation Oncology, Alfred Health and Monash University, Melbourne, VIC (Australia); Andrianopoulos, Nick [Department of Epidemiology and Preventive Medicine, Monash University School of Public Health, Melbourne, VIC (Australia); Matheson, Bronwyn [Department of Radiation Oncology, Alfred Health and Monash University, Melbourne, VIC (Australia); Royce, Peter [Department of Urology, Alfred Health and Monash University, Melbourne, VIC (Australia); Millar, Jeremy L., E-mail: jeremy.millar@med.monash.edu.a [Department of Radiation Oncology, Alfred Health and Monash University, Melbourne, VIC (Australia); Department of Epidemiology and Preventive Medicine, Monash University School of Public Health, Melbourne, VIC (Australia)

2011-01-01T23:59:59.000Z

218

Microhydration Effects on the Intermediates of the SN2 Reacation of Iodide Anion with Methyl Iodine  

SciTech Connect

Reactions of halide anions with methyl halides (X- + CH3Y ? XCH3 + Y-) are bimolecular nucleophilic substitution (SN2) reactions that have been well investigated in the last few decades.[1] Figure 1 shows typical potential energy surfaces (PESs) proposed for symmetric (X- + CH3X ? XCH3 + X-) SN2 reactions along the reaction coordinate. In the gas phase, the PES has two minima corresponding to the stable X-(CH3X) complexes.[2] The PES is substantially distorted by the solvation. Since the negative charge is delocalized over the [X•••CH3•••X]- moiety at the transition state the stabilization energy gained by the solvation is smaller for the transition state than that for the (X- + CH3X) reactants or the X- (CH3X) complexes. In solution, a large potential barrier exists between the reactants and products. The rate constants of these reactions in protic solvents were reported to be a few orders of magnitude smaller than those in aprotic solvents; this trend was explained by the formation of solvation shells of protic molecules around the halide anions.[1,3] Morokuma has previously reported a theoretical study on the PES of the (Cl- + CH3Cl ? ClCH3 + Cl-) SN2 reaction with a few H2O molecules. The attachment of H2O molecules to the Cl-(CH3Cl) reactive system produces metastable isomers, which affect the reaction mechanism.[4] Johnson and coworkers extensively investigated the structure and reactions of halide anion complexes in the gas phase using photodissociation spectroscopy.

Doi, Keisuke; Togano, Eijiro; Xantheas, Sotiris S.; Nakanishi, Ryuzo; Nagata, Takashi; Ebata, Takayuki; Inokuchi, Yoshiya

2013-04-15T23:59:59.000Z

219

Interfacing the tandem mirror reactor to the sulfur-iodine process for hydrogen production  

DOE Green Energy (OSTI)

The blanket is linked to the H/sub 2/SO/sub 4/ vaporization units and SO/sub 3/ decomposition reactor with either sodium or helium. The engineering and safety problems associated with these choices are discussed. This H/sub 2/SO/sub 4/ step uses about 90% of the TMR heat and is best close-coupled to the nuclear island. The rest of the process we propose to be driven by steam and does not require close-coupling. The sodium loop coupling seems to be preferable at this time. We can operate with a blanket around 1200 K and the SO/sub 3/ decomposer around 1050 K. This configuration offers double-barrier protection between Li-Na and the SO/sub 3/ process gases. Heat pipes offer an attractive alternate to provide an additional barrier, added modularity for increased reliability, and tritium concentration and isolation operations with very little thermal penalty.

Galloway, T.R.

1980-06-02T23:59:59.000Z

220

Summary of the Sulfur-Iodine Process Integrated Laboratory-Scale Experiment  

Science Conference Proceedings (OSTI)

Technical Paper / Safety and Technology of Nuclear Hydrogen Production, Control, and Management / Nuclear Hydrogen Production

Benjamin Russ; Robert Buckingham; Lloyd Brown; Robert Moore; Max Helie; Philippe Carle; Nicolas Pons; Denis Ode; Jean Duhamet; Jean Leybros

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


221

Iodine-129 in forage and deer on the Hanford site and other Pacific Northwest locations  

SciTech Connect

Samples of surface soil, litter, forage, and deer (rumen content, muscle, liver, and thyroid gland) were collected from Bend, Oregon; Centralia, Washington; Wenatchee, Washington; the Wooten Game Range near Dayton, Washington; and on or near the Hanford Site, Richland, Washington. The concentrations of /sup 129/I and /sup 127/I were determined using neturon activation techniques. The purpose of the study was to establish the current levels of /sup 129/I in the environs of the Hanford Site prior to the proposed restart of fuel reprocessing at the PUREX plant. The results of this study clearly demonstrated the longevity of /sup 129/I in the biosphere following gaseous release from a nuclear facility. Analyses of thyroid glands showed that deer living within 160 km (Wooten Game Range) of Hanford had elevated levels of /sup 129/I when compared to the more distant Pacific Northwest locations (Centralia, or Bend). Levels of /sup 129/I in deer thyroid from Bend, or Centralia, (15 fCi/g wet weight), were about five times higher than values reported for the central United States, while, Hanford samples were about 2,700 times higher. The average concentration of /sup 129/I in deer thyroids collected at Hanford in 1978 was similar to samples collected 14 years earlier. The concentrations of /sup 129/I in soil, litter, forage, and other deer samples generally decrease in the order: Hanford > Wooten > Wenatchee > Centralia approx. = Bend. This corresponds to an increase in distance from the Hanford Site.

Price, K.R.; Cadwell, L.L.; Schreckhise, R.G.; Brauer, F.P.

1981-02-01T23:59:59.000Z

222

Capture of Solar and Higher-Energy Neutrinos by Iodine 127  

E-Print Network (OSTI)

We discuss and improve a recent treatment of the absorption of solar neutrinos by ${}^{127}$I, in connection with a proposed solar neutrino detector. With standard-solar-model fluxes and an in-medium value of -1.0 for the axial-vector coupling constant $g_A$, we obtain a ${}^8$B-neutrino cross section of 3.3$\\times 10^{-42}$, about 50\\% larger than in our previous work, and a ${}^7$Be cross section that is less certain but nevertheless also larger than before. We then apply the improved techniques to higher incoming energies that obtain at the LAMPF beam dump, where an experiment is underway to finalize a calibration of the ${}^{127}$I with electron neutrinos from muon decay. We find that forbidden operators, which play no role in solar-neutrino absorption, contribute nonnegligibly to the LAMPF cross section, and that the preliminary LAMPF mean value is significantly larger than our prediction.

J. Engel; S. Pittel; P. Vogel

1994-02-17T23:59:59.000Z

223

Ocular Response of Choroidal Melanoma With Monosomy 3 Versus Disomy 3 After Iodine-125 Brachytherapy  

SciTech Connect

Purpose: To report the ocular response of choroidal melanoma with monosomy 3 vs. disomy 3 after {sup 125}I brachytherapy. Methods and Materials: We evaluated patients with ciliochoroidal melanoma managed with fine needle aspiration biopsy immediately before plaque application for {sup 125}I brachytherapy between January 1, 2005 and December 31, 2008. Patients with (1) cytopathologic diagnosis of melanoma, (2) melanoma chromosome 3 status identified by fluorescence in situ hybridization, and (3) 6 or more months of follow-up after brachytherapy were sorted by monosomy 3 vs. disomy 3 and compared by Kruskal-Wallis test. Results: Among 40 ciliochoroidal melanomas (40 patients), 15 had monosomy 3 and 25 had disomy 3. Monosomy 3 melanomas had a median greatest basal diameter of 12.00 mm and a median tumor thickness of 6.69 mm before brachytherapy; at a median of 1.75 years after brachytherapy, median thickness was 3.10 mm. Median percentage decrease in tumor thickness was 48.3%. Disomy 3 melanomas had a median greatest basal diameter of 10.00 mm and median tumor thickness of 3.19 mm before brachytherapy; at a median of 2.00 years after brachytherapy, median tumor thickness was 2.37 mm. The median percentage decrease in tumor thickness was 22.7%. Monosomy 3 melanomas were statistically greater in size than disomy 3 melanomas (p < 0.001) and showed a greater decrease in tumor thickness after brachytherapy (p = 0.006). Conclusion: In this study, ciliochoroidal melanomas with monosomy 3 were significantly greater in size than disomy 3 melanoma and showed a significantly greater decrease in thickness at a median of 1.75 years after brachytherapy. The greater decrease in monosomy 3 melanoma thickness after brachytherapy is consistent with other malignancies in which more aggressive pathology has been shown to be associated with a greater initial response to radiotherapy.

Marathe, Omkar S. [David Geffen School of Medicine, University of Los Angeles, Los Angeles, CA (United States); Wu, Jeffrey; Lee, Steve P. [Department of Radiation Oncology, University of Los Angeles, Los Angeles, CA (United States); Yu Fei; Burgess, Barry L. [Department of Ophthalmology, The Jules Stein Eye Institute, University of Los Angeles, Los Angeles, CA (United States); Leu Min [Department of Radiation Oncology, University of Los Angeles, Los Angeles, CA (United States); Straatsma, Bradley R. [Department of Ophthalmology, The Jules Stein Eye Institute, University of Los Angeles, Los Angeles, CA (United States); McCannel, Tara A., E-mail: TMcCannel@jsei.ucla.edu [Department of Ophthalmology, Jules Stein Eye Institute, University of Los Angeles, Los Angeles, CA (United States); Jonsson Comprehensive Cancer Center, University of Los Angeles, Los Angeles, CA (United States)

2011-11-15T23:59:59.000Z

224

Solar-Grade Silicon from Metallurgical-Grade Silicon Via Iodine Chemical Vapor Transport Purification: Preprint  

DOE Green Energy (OSTI)

This conference paper describes the atmospheric-pressure in an ''open'' reactor, SiI2 transfers from a hot (>1100C) Si source to a cooler (>750C) Si substrate and decomposes easily via 2SiI2 Si+ SiI4 with up to 5?m/min deposition rate. SiI4 returns to cyclically transport more Si. When the source is metallurgical-grade Si, impurities can be effectively removed by three mechanisms: (1) differing free energies of formation in forming silicon and impurity iodides; (2) distillation; and (3) differing standard free energies of formation during deposition. Distillation has been previously reported. Here, we focused on mechanisms (1) and (3). We made feedstock, analyzed the impurity levels, grew Czochralski single crystals, and evaluated crystal and photovoltaic properties. Cell efficiencies of 9.5% were obtained. Incorporating distillation (step 2) should increase this to a viable level.

Ciszek, T. F.; Wang, T. H.; Page, M. R.; Bauer, R. E.; Landry, M. D.

2002-05-01T23:59:59.000Z

225

University of Mississippi Medical Center Page 1 of 186  

E-Print Network (OSTI)

................................................................................84 E. Liquid Waste Disposal-125 and/or Iodine- 131 in capsule form or a total of (1) millicurie of liquid Iodine-125 and/or Iodine

Correia, John J.

226

NANOCOMPOSITE ENABLED SENSITIZED SOLAR CELL  

E-Print Network (OSTI)

Fluorine-Doped Tin Oxide ITO – Indium-Doped Tin Oxide DI –used in DSSCs: indium-doped tin oxide (ITO) and fluorine-

Phuyal, Dibya

2012-01-01T23:59:59.000Z

227

Graphene and its Hybrid Nanostructures for Nanoelectronics and Energy Applications  

E-Print Network (OSTI)

nanowire arrays on an indium tin oxide substrate. Journal ofmetal oxides such as indium tin oxide (ITO) or fluorine tinoptoelectronics are indium tin oxide (ITO) and fluorine tin

LIN, JIAN

2011-01-01T23:59:59.000Z

228

Plutonium complexation by phosphonate-functionalized mesoporous silica  

Science Conference Proceedings (OSTI)

MCM-41-type mesoporous silica functionalized with the CMPO-based 'Ac-Phos' silane has been reported in the literature (1) to show good capacity as an acftinide sorbent material, with potential applications in environmental sequestration, aqueous waste separation and/or vitrification, and chemical sensing of actinides in solution. The study explores the complexation of Pu(IV and VI) and other selected actinides and lanthanides by SBA-15 type mesoporous silica functionalized with Ac-Phos. The Pu binding kinetics and binding capacity were determined for both the Ac-Phos functionalized and unmodified SBA-15. They analyzed the binding geometry and redox behavior of Pu(VI) by X-ray absorption spectroscopy (XAS). They discuss the synthesis and characterization of the functionalized mesoporous material, batch sorption experiments, and the detailed analyses of the actinide complexes that are formed. Structural measurements are paired with high-level quantum mechanical modeling to elucidate the binding mechanisms.

Parsons-Moss, T; Schwaiger, L K; Hubaud, A; Hu, Y J; Tuysuz, H; Yang, P; Balasubramanian, K; Nitsche, H

2010-10-27T23:59:59.000Z

229

SYNTHESIS OF A NEW FAMILY OF FLUORINATED BORONATE COMPOUNDS AS ANION RECEPTORS AND STUDIES OF THEIR USE AS ADDITIVES IN LITHIUM BATTERY ELECTROLYTES.  

DOE Green Energy (OSTI)

Numerous studies have been done on developing new electrolytes for lithium batteries with high ionic conductivity, and good chemical and electrochemical stability. In addition to the research on new salts and solvents, the use of cation receptors to reduce ion pairing in non-aqueous electrolytes has been considered as an approach to improve the properties of electrolytes. Although both cation and anion receptors enhance the dissociation of ion pairs and increase the conductivity of electrolytes, the use of anion receptors is more attractive for a lithium battery electrolyte because anion receptors increase the lithium transference number in the electrolyte. However, most available neutral anion receptors complex with anions through hydrogen binding and cannot be used in lithium batteries. Recently, we have reported on synthesis of a series of new neutral boron compounds as anion receptors based on the idea that electron-deficient boron would complex the anion of the ion pair. The anion complexation effect of these boron compounds was further enhanced by attaching electron-withdrawing groups. Here we report synthesis of another new family of boronate compounds. The effect of these new compounds on conductivity of lithium salts in non-aqueous solution was studied. The molecular weights of these new boronate compounds are lower than our previously reported boron compounds. Therefore, their effects on conductivity enhancement are superior. They also display high electrochemical stability up to 5 V.

MCBREEN,J.; LEE,H.S.; YANG,X.Q.

2001-06-08T23:59:59.000Z

230

Properties of small molecular drug loading and diffusion in a fluorinated PEG hydrogel studied by 1H molecular diffusion NMR and 19F spin diffusion NMR  

E-Print Network (OSTI)

of Technology, Pasadena, CA 91125, USA NMR combined withspin diffusion NMR is useful in studying the drug loadingdiffusion . Spin diffusion . NMR Introduction R f -PEGs (

Mathias, Errol V.; Aponte, Julia; Kornfield, Julia A.; Ba, Yong

2010-01-01T23:59:59.000Z

231

Phenyl boron-based compounds as anion receptors for non-aqueous battery electrolytes  

SciTech Connect

Novel fluorinated boronate-based compounds which act as anion receptors in non-aqueous battery electrolytes are provided. When added to non-aqueous battery electrolytes, the fluorinated boronate-based compounds of the invention enhance ionic conductivity and cation transference number of non-aqueous electrolytes. The fluorinated boronate-based anion receptors include different fluorinated alkyl and aryl groups.

Lee, Hung Sui (East Setauket, NY); Yang, Xiao-Qing (Port Jefferson Station, NY); McBreen, James (Bellport, NY); Sun, Xuehui (Middle Island, NY)

2002-01-01T23:59:59.000Z

232

Characterization of a New Charge Sensitive Preamplifier (CSP) for the Electromagnetic Calorimeters of the ALICE Experiment  

Science Conference Proceedings (OSTI)

The ALICE calorimeters PHOS and EMCal (including its extension DCal) are based on Avalanche Photo-Diode (APD) photosensors with Charge Sensitive Preamplifiers (CSPs) for readout of the scintillating elements. A new CSP has been developed on the basis of the design of the PHOS CSP, but modified to meet the requirements of the EMCal and DCal. Modifications were made specifically for a different APD choice with different characteristics, and also with the goals of less noise, faster rise time, and reduced cost. This paper presents a detailed description of the new CSP features and the test results.

Wang, Yaping [Inst. of Particle Physics/Key Lab. of Quark and Lepton Physics, Central China Normal Univ., Wuhan, C; Muller, Hans [CERN, Geneva, Switzerland; Cai, Xu [Inst. of Particle Physics/Key Lab. of Quark and Lepton Physics, Central China Normal Univ., Wuhan, C; Zhou, Daicui [Inst. of Particle Physics/Key Lab. of Quark and Lepton Physics, Central China Normal Univ., Wuhan, C; Awes, Terry C [ORNL; Yin, Zhongbao [Inst. of Particle Physics/Key Lab. of Quark and Lepton Physics, Central China Normal Univ., Wuhan, C

2012-01-01T23:59:59.000Z

233

Heterogenization of Homogeneous Catalysts: the Effect of the Support  

DOE Green Energy (OSTI)

We have studied the influence of placing a soluble, homogeneous catalyst onto a solid support. We determined that such a 'heterogenized' homogeneous catalyst can have improved activity and selectivity for the asymmetric hydrogenation of enamides to amino acid derivatives. The route of heterogenization of RhDuPhos(COD){sup +} cations occurs via electrostatic interactions with anions that are capable of strong hydrogen bonding to silica surfaces. This is a novel approach to supported catalysis. Supported RhDuPhos(COD){sup +} is a recyclable, non-leaching catalyst in non-polar media. This is one of the few heterogenized catalysts that exhibits improved catalytic performance as compared to its homogeneous analog.

Earl, W.L.; Ott, K.C.; Hall, K.A.; de Rege, F.M.; Morita, D.K.; Tumas, W.; Brown, G.H.; Broene, R.D.

1999-06-29T23:59:59.000Z

234

A Combined Gas-Phase Photoelectron Spectroscopic and Theoretical Study of Zeise's Anion and Its Bromine and Iodine Analogues  

SciTech Connect

We report the first photoelectron spectroscopic study of Zeise’s anion, [PtCl3(C2H4)], and its Br- and I- analogs in the gas phase. Well-resolved and rich spectral features are obtained for each species, yielding detailed electronic structure information, which is assigned with the aid of highlevel electronic structure calculations at the Coupled Cluster (CC) level of theory. The electron binding energies of [PtX3(C2H4)] are found to decrease with the size of halogen (4.57, 4.51, and 4.18 eV for X = Cl, Br, and I, respectively). The calculations indicate a synergistic ?2 interaction [with interaction strengths of 1.54 (Cl), 1.37 (Br) and 1.10 eV (I)] between the perpendicular C2H4 fragment and the nearly horizontal planar PtX3- anions, resulting in activating the ethylene molecule. The detailed insights of the chemical bonding and underlying electronic structure can be used to benchmark interactions between olefins and transition metal complexes, which are crucial to a wide range of catalytic processes.

Hou, Gaolei; Wen, Hui; Lopata, Kenneth A.; Zheng, Weijun; Kowalski, Karol; Govind, Niranjan; Wang, Xue B.; Xantheas, Sotiris S.

2012-06-25T23:59:59.000Z

235

Iodine Pathways and Off-Gas Stream Characteristics for Aqueous Reprocessing Plants – A Literature Survey and Assessment  

SciTech Connect

Used nuclear fuel is currently being reprocessed in only a few countries, notably France, England, Japan, and Russia. The need to control emissions of the gaseous radionuclides to the air during nuclear fuel reprocessing has already been reported for the entire plant. But since the gaseous radionuclides can partition to various different reprocessing off-gas streams, for example, from the head end, dissolver, vessel, cell, and melter, an understanding of each of these streams is critical. These off-gas streams have different flow rates and compositions and could have different gaseous radionuclide control requirements, depending on how the gaseous radionuclides partition. This report reviews the available literature to summarize specific engineering data on the flow rates, forms of the volatile radionuclides in off-gas streams, distributions of these radionuclides in these streams, and temperatures of these streams. This document contains an extensive bibliography of the information contained in the open literature.

R. T. Jubin; D. M. Strachan; N. R. Soelberg

2013-09-01T23:59:59.000Z

236

Long-Term Results of Brachytherapy With Temporary Iodine-125 Seeds in Children With Low-Grade Gliomas  

SciTech Connect

Purpose: To retrospectively review the results of temporary I-125 brachytherapy in 94 children and adolescents with low-grade glioma. Methods and Materials: Treatment was performed in progressive tumors roughly spherical in shape with a diameter of up to 5 cm, including 79 astrocytomas, 5 oligodendrogliomas, 4 oligoastrocytomas, 1 ependymoma, and 5 other tumors. Location was suprasellar/chiasmal in 44, thalamic/basal ganglia in 18, hemispheric in 15, midbrain/pineal region in 13, and lower brainstem in 3. Initially, 8% of patients were free of symptoms, 47% were symptomatic but not disabled, and 30% were slightly, 6% moderately, and 3% severely disabled. Results: 5- and 10-year survival was 97% and 92%. The response to I-125 brachytherapy over the long term was estimated after a median observation period of 38.4 (range, 6.4-171.0) months. At that time, 4 patients were in complete, 27 in partial, and 18 in objective remission; 15 showed stable and 30 progressive tumors. Treatment results did not correlate with age, sex, histology, tumor size, location, or demarcation of the tumor. Secondary treatment became necessary in 36 patients, including 19 who underwent repeated I-125 brachytherapy. At final follow-up, the number of symptom-free patients had risen to 21%. Thirty-eight percent showed symptoms without functional impairment, 19% were slightly and 11% moderately disabled, and only 4% were severely disabled. Conclusions: Response rates similar to those of conventional radiotherapy or chemotherapy can be anticipated with I-125 brachytherapy in tumors of the appropriate size and shape. We believe it to be a useful contribution to the treatment of low-grade gliomas in children.

Korinthenberg, Rudolf, E-mail: rudolf.korinthenberg@uniklinik-freiburg.d [Division of Neuropaediatrics and Muscular Disorders, Department of Paediatrics and Adolescent Medicine, University Hospital, Albert-Ludwigs University, Freiburg im Breisgau (Germany); Neuburger, Daniela [Division of Neuropaediatrics and Muscular Disorders, Department of Paediatrics and Adolescent Medicine, University Hospital, Albert-Ludwigs University, Freiburg im Breisgau (Germany); Trippel, Michael; Ostertag, Christoph; Nikkhah, Guido [Department of Stereotactic Neurosurgery, Neurocentre, University Hospital, Albert-Ludwigs University, Freiburg im Breisgau (Germany)

2011-03-15T23:59:59.000Z

237

NEMA NU4-2008 performance evaluation for the microPET FOCUS 120 and iodine-124  

Science Conference Proceedings (OSTI)

This study aimed to evaluate the performance of the microPET FOCUS 120 in terms of counting rate capability and image quality when using {sup 124}I. The noise equivalent count rate (NECR) index was defined as: NECR = R{sub T}{sup 2}/R{sub P} + R{sub GP} (T = true, P = prompt, GP = gamma prompt). The maximum NECR (48 kcps) value was obtained for the 250-590 keV energy window (EW) with 6 ns time window (TW). The two other EW (350-590 and 350-650 keV) gave comparable maximum NECR of 43 kcps for the 6 ns TW. The 2 ns TW reduced the NECR by 45 to 50 % Scatter and gamma plus scatter fractions were almost not TW dependent. The 250-590 keV window showed the largest scatter fraction with 23% For the NEMA NU4-2008 image quality phantom, coefficients of variation in the uniform part increased from about 8 to 12% when decreasing TW from 6 to 2 ns. The lowest spill-over-ratios (SOR) for the non emitting regions were obtained for the 350-590 and 350-650 keV EW. Recovery coefficients (RC) of the hot rods were the highest for the 350-590 keV EW and 2 ns TW. Scatter correction led to a decrease in RC and occasionally (with FBP or 3DRP) to a negative value for the SOR. The combination of the 350-590 keV energy window with 6 ns time window appeared to be a good compromise between counting rate capability and image quality for the FOCUS 120, especially when MAP reconstruction was used. The scatter correction algorithm provided by the constructor should be used with caution. (authors)

Taleb, D. [Experimental Medical Imaging Laboratory, Inst. of Physics B5, Univ. of Liege, 4000 Liege (Belgium); Bahri, M. A.; Warnock, G.; Salmon, E.; Luxen, A.; Plenevaux, A. [Cyclotron Research Center, Univ. of Liege, 4000 Liege (Belgium); Dartial, N. [Medical imaging laboratory ONIRIS, Nantes (France); Seret, A. [Experimental Medical Imaging Laboratory, Inst. of Physics B5, Univ. of Liege, 4000 Liege (Belgium)

2011-07-01T23:59:59.000Z

238

EchoSeed Model 6733 Iodine-125 brachytherapy source: Improved dosimetric characterization using the MCNP5 Monte Carlo code  

Science Conference Proceedings (OSTI)

This study primarily aimed to obtain the dosimetric characteristics of the Model 6733 {sup 125}I seed (EchoSeed) with improved precision and accuracy using a more up-to-date Monte-Carlo code and data (MCNP5) compared to previously published results, including an uncertainty analysis. Its secondary aim was to compare the results obtained using the MCNP5, MCNP4c2, and PTRAN codes for simulation of this low-energy photon-emitting source. The EchoSeed geometry and chemical compositions together with a published {sup 125}I spectrum were used to perform dosimetric characterization of this source as per the updated AAPM TG-43 protocol. These simulations were performed in liquid water material in order to obtain the clinically applicable dosimetric parameters for this source model. Dose rate constants in liquid water, derived from MCNP4c2 and MCNP5 simulations, were found to be 0.993 cGyh{sup -1} U{sup -1} ({+-}1.73%) and 0.965 cGyh{sup -1} U{sup -1} ({+-}1.68%), respectively. Overall, the MCNP5 derived radial dose and 2D anisotropy functions results were generally closer to the measured data (within {+-}4%) than MCNP4c and the published data for PTRAN code (Version 7.43), while the opposite was seen for dose rate constant. The generally improved MCNP5 Monte Carlo simulation may be attributed to a more recent and accurate cross-section library. However, some of the data points in the results obtained from the above-mentioned Monte Carlo codes showed no statistically significant differences. Derived dosimetric characteristics in liquid water are provided for clinical applications of this source model.

Mosleh-Shirazi, M. A.; Hadad, K.; Faghihi, R.; Baradaran-Ghahfarokhi, M.; Naghshnezhad, Z.; Meigooni, A. S. [Center for Research in Medical Physics and Biomedical Engineering and Physics Unit, Radiotherapy Department, Shiraz University of Medical Sciences, Shiraz 71936-13311 (Iran, Islamic Republic of); Radiation Research Center and Medical Radiation Department, School of Engineering, Shiraz University, Shiraz 71936-13311 (Iran, Islamic Republic of); Comprehensive Cancer Center of Nevada, Las Vegas, Nevada 89169 (United States)

2012-08-15T23:59:59.000Z

239

Phosphoinositide 3-kinase: a critical signalling event in pulmonary cells  

E-Print Network (OSTI)

of 3-D-phosphorylated phos- phoinositides in C5a-stimulated eosinophils. Biochem Biophys Res Commun 2000, 269:816–821. 18. Pan ZK, Chen LY, Cochrane CG, Zuraw BL: fMet-leu-phe stimulates proinflammatory cytokine gene expression in human peripheral blood...

2000-06-08T23:59:59.000Z

240

Welcome alumni and friends to the 2007 edition of the G-Hawker. The Department of Geology has done remarkably well over the last year, and I  

E-Print Network (OSTI)

. & FALGUEIRETTES, J. (1973). Acta Cryst. B29, 1623-1630. EMMERSON, D. S. & CORBRIDGE,D. E. C. (1972). Phos- phorus,W. T. (1965). J. Chem. Phys. 42, 3175-3187. Acta Cryst. (1973). B29, 2918 The Crystal Structure Sciences, Columbia UniversiO', New York, New York 10027, U.S.A. (Received 8 February 1973; accepted 30 July

Peterson, Blake R.

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


241

The Macroecology of Sustainability Joseph R. Burger1  

E-Print Network (OSTI)

scales. Over the past few decades, decreasing per capita rates of consumption of petroleum, phos- phate that should be integral to sustainability science: 1) physical conservation laws gov- ern the flows of energy of scientists, politicians, and lay people--and for good reason. There is increasing evidence that we have ap

Nekola, Jeffrey C.

242

Fluorspar  

NLE Websites -- All DOE Office Websites (Extended Search)

Fluorspar Fluorspar Nature Bulletin No. 361-A December 6, 1969 Forest Preserve District of Cook County George W. Dunne, President Roland F. Eisenbeis, Supt. of Conservation FLUORSPAR Among all the states, Illinois stands at the top or very near the top in its production of corn, hogs, soybeans, oats and chickens. The same is true in industries: meat packing, steel, agricultural machinery, tractors, radios, telephones, paint, candy and many others. It is one of the leading producers of coal. Not commonly known, however, is the fact that the world's largest fluorite mines are located in Pope and Hardin counties along the Ohio River, and few people realize what an important part this mineral plays in our daily lives. Chlorine, bromine, iodine and fluorine are chemical elements always found in combination with some metal. Common salt is chloride of sodium. Fluorspar, or Fluorite, is fluoride of calcium. Although quite common, occurring in several states and in foreign countries, there are few deposits with veins large enough to be mined commercially. Almost half of what is used in this country comes from southern Illinois and most of the remainder from Kentucky, just across the river. It is mined from veins as much as 800 feet below the surface.

243

It's Elemental - The Periodic Table of Elements - Elements Listed by Atomic  

NLE Websites -- All DOE Office Websites (Extended Search)

Atomic Number Atomic Number 1 Hydrogen H 2 Helium He 3 Lithium Li 4 Beryllium Be 5 Boron B 6 Carbon C 7 Nitrogen N 8 Oxygen O 9 Fluorine F 10 Neon Ne 11 Sodium Na 12 Magnesium Mg 13 Aluminum Al 14 Silicon Si 15 Phosphorus P 16 Sulfur S 17 Chlorine Cl 18 Argon Ar 19 Potassium K 20 Calcium Ca 21 Scandium Sc 22 Titanium Ti 23 Vanadium V 24 Chromium Cr 25 Manganese Mn 26 Iron Fe 27 Cobalt Co 28 Nickel Ni 29 Copper Cu 30 Zinc Zn 31 Gallium Ga 32 Germanium Ge 33 Arsenic As 34 Selenium Se 35 Bromine Br 36 Krypton Kr 37 Rubidium Rb 38 Strontium Sr 39 Yttrium Y 40 Zirconium Zr 41 Niobium Nb 42 Molybdenum Mo 43 Technetium Tc 44 Ruthenium Ru 45 Rhodium Rh 46 Palladium Pd 47 Silver Ag 48 Cadmium Cd 49 Indium In 50 Tin Sn 51 Antimony Sb 52 Tellurium Te 53 Iodine I 54 Xenon Xe 55 Cesium Cs 56 Barium Ba 57 Lanthanum La 58 Cerium Ce

244

It's Elemental - The Periodic Table of Elements - Elements Listed by  

NLE Websites -- All DOE Office Websites (Extended Search)

Chemical Name Chemical Name Actinium Ac 89 Aluminum Al 13 Americium Am 95 Antimony Sb 51 Argon Ar 18 Arsenic As 33 Astatine At 85 Barium Ba 56 Berkelium Bk 97 Beryllium Be 4 Bismuth Bi 83 Bohrium Bh 107 Boron B 5 Bromine Br 35 Cadmium Cd 48 Calcium Ca 20 Californium Cf 98 Carbon C 6 Cerium Ce 58 Cesium Cs 55 Chlorine Cl 17 Chromium Cr 24 Cobalt Co 27 Copernicium Cn 112 Copper Cu 29 Curium Cm 96 Darmstadtium Ds 110 Dubnium Db 105 Dysprosium Dy 66 Einsteinium Es 99 Erbium Er 68 Europium Eu 63 Fermium Fm 100 Flerovium Fl 114 Fluorine F 9 Francium Fr 87 Gadolinium Gd 64 Gallium Ga 31 Germanium Ge 32 Gold Au 79 Hafnium Hf 72 Hassium Hs 108 Helium He 2 Holmium Ho 67 Hydrogen H 1 Indium In 49 Iodine I 53 Iridium Ir 77 Iron Fe 26 Krypton Kr 36 Lanthanum La 57 Lawrencium Lr 103 Lead Pb 82 Lithium Li 3 Livermorium Lv 116

245

Treatment of plutonium process residues by molten salt oxidation  

Science Conference Proceedings (OSTI)

Molten Salt Oxidation (MSO) is a thermal process that can remove more than 99.999% of the organic matrix from combustible {sup 238}Pu material. Plutonium processing residues are injected into a molten salt bed with an excess of air. The salt (sodium carbonate) functions as a catalyst for the conversion of the organic material to carbon dioxide and water. Reactive species such as fluorine, chlorine, bromine, iodine, sulfur, phosphorous and arsenic in the organic waste react with the molten salt to form the corresponding neutralized salts, NaF, NaCl, NaBr, NaI, Na{sub 2}SO{sub 4}, Na{sub 3}PO{sub 4} and NaAsO{sub 2} or Na{sub 3}AsO4. Plutonium and other metals react with the molten salt and air to form metal salts or oxides. Saturated salt will be recycled and aqueous chemical separation will be used to recover the {sup 238}Pu. The Los Alamos National Laboratory system, which is currently in the conceptual design stage, will be scaled down from current systems for use inside a glovebox.

Stimmel, J.; Wishau, R.; Ramsey, K.B.; Montoya, A.; Brock, J. [Los Alamos National Lab., NM (United States); Heslop, M. [Naval Surface Warfare Center (United States). Indian Head Div.; Wernly, K. [Molten Salt Oxidation Corp. (United States)

1999-04-01T23:59:59.000Z

246

It's Elemental - The Periodic Table of Elements - Elements Listed by  

NLE Websites -- All DOE Office Websites (Extended Search)

Chemical Symbol Chemical Symbol Ac Actinium 89 Ag Silver 47 Al Aluminum 13 Am Americium 95 Ar Argon 18 As Arsenic 33 At Astatine 85 Au Gold 79 B Boron 5 Ba Barium 56 Be Beryllium 4 Bh Bohrium 107 Bi Bismuth 83 Bk Berkelium 97 Br Bromine 35 C Carbon 6 Ca Calcium 20 Cd Cadmium 48 Ce Cerium 58 Cf Californium 98 Cl Chlorine 17 Cm Curium 96 Cn Copernicium 112 Co Cobalt 27 Cr Chromium 24 Cs Cesium 55 Cu Copper 29 Db Dubnium 105 Ds Darmstadtium 110 Dy Dysprosium 66 Er Erbium 68 Es Einsteinium 99 Eu Europium 63 F Fluorine 9 Fe Iron 26 Fl Flerovium 114 Fm Fermium 100 Fr Francium 87 Ga Gallium 31 Gd Gadolinium 64 Ge Germanium 32 H Hydrogen 1 He Helium 2 Hf Hafnium 72 Hg Mercury 80 Ho Holmium 67 Hs Hassium 108 I Iodine 53 In Indium 49 Ir Iridium 77 K Potassium 19 Kr Krypton 36 La Lanthanum 57 Li Lithium 3 Lr Lawrencium 103

247

University of Mississippi Medical Center Page 1 of 181  

E-Print Network (OSTI)

-125 and/or Iodine- 131 in capsule form or a total of (1) millicurie of liquid Iodine-125 and/or Iodine Radioactive Material Do Not Empty". G. Each sink used for liquid waste disposal or cleaning of contaminated

Raucher, Drazen

248

Development of novel transition metal-catalyzed cross-coupling reactions and applications thereof  

E-Print Network (OSTI)

Chapter 1 The first example of Pd(0)/(II) catalyzed fluorination of aryl bromides is reported herein. Based on these data, an analogous method was developed for the fluorination of aryl triflates. The reaction proceeds ...

Teverovskiy, Georgiy

2013-01-01T23:59:59.000Z

249

NIST - Physical and Chemical Properties Division - Technical ...  

Science Conference Proceedings (OSTI)

... suppressant. Thus although fluorine can remove hydrogen atoms, the hydrogen fluoride that is formed cannot be recycled. ...

250

CNST NanoFab Group  

Science Conference Proceedings (OSTI)

... silicon RIE (Reactive Ion Etching), several fluorine based RIE systems including cryogenic cooled etches, ion milling and xenon fluoride etching. ...

2013-09-25T23:59:59.000Z

251

Boron compounds as anion binding agents for nonaqueous battery electrolytes  

DOE Patents (OSTI)

Novel fluorinated boron-based compounds which act as anion receptors in non-aqueous battery electrolytes are provided. When added to non-aqueous battery electrolytes, the fluorinated boron-based compounds of the invention enhance ionic conductivity and cation transference number of non-aqueous electrolytes. The fluorinated boron-based anion receptors include borane and borate compounds bearing different fluorinated alkyl and aryl groups.

Lee, Hung Sui (East Setauket, NY); Yang, Xia-Oing (Port Jefferson Station, NY); McBreen, James (Bellport, NY); Xiang, Caili (Upton, NY)

2000-02-08T23:59:59.000Z

252

Tech Beat January 8, 2008  

Science Conference Proceedings (OSTI)

... accurate measurements of the fluorine-18 isotopes. ... standard reference material for this isotope. ... research and development programs in metrology. ...

2012-03-19T23:59:59.000Z

253

Multivitamin/Multielement Dietary Supplement SRM  

Science Conference Proceedings (OSTI)

... chromium, copper, iodine, iron, magnesium, manganese, molybdenum, nickel, phosphorous, potassium, selenium, silicon, tin, vanadium, and zinc. ...

2012-10-22T23:59:59.000Z

254

Physical features of small disperse coal dust fraction transportation and structurization processes in iodine air filters of absorption type in ventilation systems at nuclear power plants  

E-Print Network (OSTI)

The research on the physical features of transportation and structurization processes by the air-dust aerosol in the granular filtering medium with the cylindrical coal adsorbent granules in an air filter of the adsorption type in the heating ventilation and cooling (HVAC) system at the nuclear power plant is completed. The physical origins of the coal dust masses distribution along the absorber with the granular filtering medium with the cylindrical coal granules during the air-dust aerosol intake process in the near the surface layer of absorber are researched. The quantitative technical characteristics of air filtering elements, which have to be considered during the optimization of air filters designs for the application in the ventilation systems at the nuclear power plants, are obtained.

Ledenyov, Oleg P; Poltinin, P Ya; Fedorova, L I

2012-01-01T23:59:59.000Z

255

DOE SBIR Phase I Grant No. DE-FG02-00ER83067, ''A Flexible and Economical Automated Nucleophilic [{sup 18}F]Fluorination synthesis System for PET Radiopharmaceuticals.'' Final Technical Report  

Science Conference Proceedings (OSTI)

Phase I Final Report. A prototype manual remote synthesis system based on the unit operations approach was designed, constructed, and functionally tested. This general-purpose system was validated by its configuration and initial use for the preparation of the PET radiopharmaceutical [F-18]FLT using [F-18]fluoride ion.

Padgett, Henry C.

2001-08-04T23:59:59.000Z

256

Looking before we leap: an ongoing, quantative investigation of asteroid and comet impact hazard mitigation  

SciTech Connect

There are many outstanding questions about the correct response to an asteroid or comet impact threat on Earth. Nuclear munitions are currently thought to be the most efficient method of delivering an impact-preventing impulse to a potentially hazardous object (PHO). However, there are major uncertainties about the response of PHOs to a nuclear burst, and the most appropriate ways to use nuclear munitions for hazard mitigation.

Plesko, Catherine S [Los Alamos National Laboratory; Weaver, Robert P [Los Alamos National Laboratory; Bradley, Paul A [Los Alamos National Laboratory; Huebner, Walter F [Los Alamos National Laboratory

2010-01-01T23:59:59.000Z

257

U.S. Department of Energy Categorical Exclusion Determination Form  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Electrochemical Fluorination in Molten Fluoride Salts Electrochemical Fluorination in Molten Fluoride Salts Savannah River Site Aiken/Aiken/South Carolina This EEC covers activities in C105/110 related to development of an electrochemical fluorination process to separate selected metals (non- RCRA) from depleted uranium. The goal of the process is to convert depleted uranium metal (U) to gaseous uranium hexafluoride (UF6) that can be easily separated from solution while other metallic constituents remain as metals or are converted to non-volatile fluoride salts. The electrochemical fluorination process will be conducted in molten fluoride eutectic salts at temperatures above 300°C. The electrochemical fluorination process will be carried out using the fluorinating agents such as NF3, XeF2, and F2. Additional inert gases or vacuum may be used in

258

U.S. Department of Energy Categorical Exclusion Determination Form  

NLE Websites -- All DOE Office Websites (Extended Search)

Electrochemical Fluorination in Molten Fluoride Salts Electrochemical Fluorination in Molten Fluoride Salts Savannah River Site Aiken/Aiken/South Carolina This EEC covers activities in C105/110 related to development of an electrochemical fluorination process to separate selected metals (non- RCRA) from depleted uranium. The goal of the process is to convert depleted uranium metal (U) to gaseous uranium hexafluoride (UF6) that can be easily separated from solution while other metallic constituents remain as metals or are converted to non-volatile fluoride salts. The electrochemical fluorination process will be conducted in molten fluoride eutectic salts at temperatures above 300°C. The electrochemical fluorination process will be carried out using the fluorinating agents such as NF3, XeF2, and F2. Additional inert gases or vacuum may be used in

259

Towards Industrial Aluminum Spent Pot Lining Treatment with ...  

Science Conference Proceedings (OSTI)

The development of a conversion process for the fluorinated end-product would allow its reuse as a substitute to fluorspar mineral for aluminum fluoride ...

260

The PICASSO Dark Matter Experiment  

Science Conference Proceedings (OSTI)

The PICASSO experiment searches for cold dark matter through the direct detection of weakly interacting massive particles (WIMPs) via their spin?dependent interactions with fluorine at SNOLAB

Ubi Wichoski; The PICASSO Collaboration

2011-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


261

Gas scrubbing liquids  

DOE Patents (OSTI)

Fully chlorinated and/or fluorinated hydrocarbons are used as gas scrubbing liquids for preventing noxious gas emissions to the atmosphere.

Lackey, Walter J. (Oak Ridge, TN); Lowrie, Robert S. (Oak Ridge, TN); Sease, John D. (Knoxville, TN)

1981-01-01T23:59:59.000Z

262

Conversion of Yellow Cake to UF6  

NLE Websites -- All DOE Office Websites (Extended Search)

Yellow cake is converted to uranium hexafluoride through a multi-step chemical process using nitric acid, ammonium hydroxide, hydrogen, hydrofluoric acid (HF) and fluorine (F2)....

263

Production and Handling Slide 18: Conversion of Yellow Cake to...  

NLE Websites -- All DOE Office Websites (Extended Search)

last step of the conversion process involves the chemical conversion of uranium tetrafluoride UF4 to uranium hexafluoride UF6 using fluorine F2. Slide 1...

264

NIST Tech Beat - March 1, 2007  

Science Conference Proceedings (OSTI)

... Computer modeling rendition of the proposed carbon-fluorine bond-breaking macrocycle after reaction with a molecule of methyl fluoride (CH3F). ...

265

Journal of Research Volume 44  

Science Conference Proceedings (OSTI)

... Heat of fluorination of cobaltous fluoride, and the heats of reaction of cobaltic fluoride with hydrogen and with bis(trifluoromethyl)benzene (a,a,a,a',a ...

2012-10-05T23:59:59.000Z

266

NIST Image Gallery: Image Details  

Science Conference Proceedings (OSTI)

... Computer modeling rendition of the proposed carbon-fluorine bond-breaking macrocycle after reaction with a molecule of methyl fluoride (CH3F). ...

267

NIST Theory of the optical properties of materials  

Science Conference Proceedings (OSTI)

... incorporating excitonic effects. The spectra shown above represent the fluorine (F) core edge in lithium fluoride (LiF). The top ...

2013-03-26T23:59:59.000Z

268

Electroslag Remelting II  

Science Conference Proceedings (OSTI)

Sep 23, 2013 ... Experimental Research on the Absorption of Fluorine in Gamma-TiAl during Electroslag Remelting: Peter Spiess1; Bernd Friedrich1; 1RWTH ...

269

Katrice Lippa  

Science Conference Proceedings (OSTI)

... Patent: Covalently Immobilized Fluorinated Carboxylic Acid Stationary Phase for Liquid Chromatography (US Patent No. 7,794,837 B2; Sep. ...

2013-06-07T23:59:59.000Z

270

The F-Gas Regulation and HFC Usage in Fire Suppression ...  

Science Conference Proceedings (OSTI)

... of more than 1 ton per annum of fluorinated greenhouse gases must report quantities exported, and any quantities of gas exported for recycling ...

2011-10-13T23:59:59.000Z

271

Chamber transport of "foot" pulses for heavy-ion fusion  

E-Print Network (OSTI)

resulting from the molten-salt jets planned for wallin Section III E, the molten-salt jets themselves arechamber transport. A molten salt composed of fluorine,

Sharp, W.M.; Callahan-Miller, D.A.; Tabak, M.; Yu, S.S.; Peterson, P.F.

2002-01-01T23:59:59.000Z

272

.sup.18 F-4-Fluoroantipyrine  

DOE Patents (OSTI)

The novel radioactive compound .sup.18 F-4-fluoroantipyrine having high specific activity which can be used in nuclear medicine in diagnostic applications, prepared by the direct fluorination of antipyrine in acetic acid with radioactive fluorine at room temperature and purifying said radioactive compound by means of gel chromatography with ethyl acetate as eluent is disclosed. The non-radioactive 4-fluoroantipyrine can also be prepared by the direct fluorination of antipyrine in acetic acid with molecular fluorine at room temperature and purified by means of gel chromotography with ethyl acetate eluent.

Shiue, Chyng-Yann (Wading River, NY); Wolf, Alfred P. (Setauket, NY)

1984-03-13T23:59:59.000Z

273

Technology Search Results | Brookhaven Technology ...  

BSA 01-04: Surface Preparation of Niobium to Enhance Quantum Efficiency of Photoelectron Yield; BSA 03-01 & 12-34: Fluorinated Precursors of ...

274

Induction slag reduction process for making titanium  

DOE Patents (OSTI)

Continuous process for preparing titanium comprising fluorinating titanium ore, and reducing the formed alkaline earth fluotitanate with an alkaline earth metal in an induction slag reactor.

Traut, Davis E. (Corvallis, OR)

1991-01-01T23:59:59.000Z

275

Sealed Gravitational Capillary Viscometry of Dimethyl Ether ...  

Science Conference Proceedings (OSTI)

... RF Hafer, Viscosity of Fluorinated Propane Isomers. ... EW Lemmon, An Equation of State for the ... Dense Fluids, Plenum Press, New York and London ...

2013-12-11T23:59:59.000Z

276

Oral Histories: Biochemist John Randolph Totter, Ph.D.  

NLE Websites -- All DOE Office Websites (Extended Search)

So, it was a concern for iodine-131 and fallout? TOTTER: Yes. And if? FISHER: -the atomic testing? TOTTER: If you followed the gross measurement and assumed that the iodine...

277

Microchemical systems for singlet oxygen generation  

E-Print Network (OSTI)

Chemical Oxygen-Iodine Lasers (COIL) are a technology of interest for industrial and military audiences. COILs are flowing gas lasers where the gain medium of iodine atoms is collisionally pumped by singlet delta oxygen ...

Hill, Tyrone F. (Tyrone Frank), 1980-

2008-01-01T23:59:59.000Z

278

AOCS Official Method Tg 2a-64  

Science Conference Proceedings (OSTI)

Iodine Value of Fatty Amines, Modified Wijs Method AOCS Official Method Tg 2a-64 Methods Downloads Methods Downloads DEFINITION The iodine value is a measure of the unsaturation of the alkyl group or groups and is

279

Microsoft Word - DOE-EIS-0281-SA-01.doc  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

other medical and research isotopes such as iodine-131, xenon-133, and iodine- 125. Irradiation of eight targets was planned in the base year, increasing to 375 targets in 2003...

280

AOCS Official Method Cd 1c-85  

Science Conference Proceedings (OSTI)

Calculated Iodine Value AOCS Official Method Cd 1c-85 Methods Methods and Analyses Analytical Chemistry Methods Downloads Methods Downloads DEFINITION This method determines the iodine value for edible oils dir

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


281

ORISE: Radiation and Radioactive Contamination FAQ  

NLE Websites -- All DOE Office Websites (Extended Search)

take potassium iodide, also known as KI? A: KI is a medication that blocks the thyroid gland from absorbing radioactive iodine. It works by providing all the iodine the gland...

282

AOCS Official Method Da 15-48  

Science Conference Proceedings (OSTI)

Iodine Value, Wijs Method AOCS Official Method Da 15-48 Methods Methods and Analyses Analytical Chemistry Methods Downloads Methods Downloads DEFINITION The iodine value is a measure of the unsaturation of the

283

AOCS Official Method Tg 3a-64  

Science Conference Proceedings (OSTI)

Iodine Value of Fatty Quaternary Ammonium Chlorides, Modified Wijs Method AOCS Official Method Tg 3a-64 Methods Downloads Methods Downloads DEFINITION The iodine value is a measure of the unsaturation of the alkyl

284

AOCS Official Method Ja 14-91  

Science Conference Proceedings (OSTI)

Iodine Value, Wijs Method AOCS Official Method Ja 14-91 Methods Downloads Methods Downloads DEFINITION The iodine value (IV) is a measure of the content of unsaturated fatty acids. The test sample is reacted with

285

AOCS Official Method Cd 1d-92  

Science Conference Proceedings (OSTI)

Iodine Value of Fats and Oils Cyclohexane-Acetic Acid Method AOCS Official Method Cd 1d-92 Methods Methods and Analyses Analytical Chemistry Methods Downloads Methods Downloads DEFINITION The iodine value is a

286

AOCS Official Method Tg 1-64  

Science Conference Proceedings (OSTI)

Iodine Value, Wijs Method AOCS Official Method Tg 1-64 Methods Downloads Methods Downloads DEFINITION The iodine value is a measure of the unsaturation of industrial oils and derivatives and is expressed in terms

287

First 2D Pictures of a 'Frequency Comb' Transform It into a ...  

Science Conference Proceedings (OSTI)

... of molecular iodine, each taken under different experimental conditions using a NIST frequency brush created with an ultrafast visible laser. ...

2010-10-05T23:59:59.000Z

288

Materials for Nuclear Power: Digital Resource Center Text Topic - TMS  

Science Conference Proceedings (OSTI)

May 21, 2007 ... Total Systems Performance Assessment (TSPA) analysis has indicated that major radionuclides contributing to dose are technetium, iodine, ...

289

It's Elemental - The Periodic Table of Elements  

NLE Websites -- All DOE Office Websites (Extended Search)

Selenium Bromine Krypton Rubidium Strontium Yttrium Zirconium Niobium Molybdenum Technetium Ruthenium Rhodium Palladium Silver Cadmium Indium Tin Antimony Tellurium Iodine...

290

Process for electrolytically preparing uranium metal  

DOE Patents (OSTI)

A process for making uranium metal from uranium oxide by first fluorinating uranium oxide to form uranium tetrafluoride and next electrolytically reducing the uranium tetrafluoride with a carbon anode to form uranium metal and CF.sub.4. The CF.sub.4 is reused in the fluorination reaction rather than being disposed of as a hazardous waste.

Haas, Paul A. (Knoxville, TN)

1989-01-01T23:59:59.000Z

291

Process for producing 8-fluoropurines  

DOE Patents (OSTI)

An efficient, regiocontrolled approach to the synthesis of 8-fluoropurines by direct fluorination of purines with dilute elemental fluorine, or acetyl hypofluorite, is provided. In a preferred embodiment, a purine compound is dissolved in a polar solvent and reacted with a dilute mixture of F.sub.2 in He or other inert gas.

Barrio, Jorge R. (Agoura Hills, CA); Satyamurthy, Nagichettiar (Los Angeles, CA); Namavari, Mohammad (Los Angeles, CA); Phelps, Michael E. (Encino, CA)

1999-01-01T23:59:59.000Z

292

8-fluoropurine compounds  

DOE Patents (OSTI)

An efficient, regiocontrolled approach to the synthesis of 8-fluoropurines by direct fluorination of purines with dilute elemental fluorine, or acetyl hypofluorite, is provided. In a preferred embodiment, a purine compound is dissolved in a polar solvent and reacted with a dilute mixture of F.sub.2 in He or other inert gas.

Barrio, Jorge R. (Agoura Hills, CA); Satyamurthy, Nagichettiar (Los Angeles, CA); Namavari, Mohammad (Los Angeles, CA); Phelps, Michael E. (Encino, CA)

2001-01-01T23:59:59.000Z

293

BASIC STUDIES OF THE SEPARATION OF URANIUM HEXAFLUORIDE FROM MIXTURES CONTAINING CHLORINE TRIFLUORIDE AND HYDROGEN FLUORIDE  

SciTech Connect

Processes for the conversion of uranium compounds or uranium metal to uranium hexafluoride ordinarily involve the use of a powerful fluorinating agent. Elemental fluorine is used when the scale of operations justifies the construction of a fluorine generating plant, but for smaller operation the use of the interhalogens of fluorine has definite advantages. These compounds provide a high concentration of fluorinating power at moderate temperatures and pressures and are more easily stored and transported than fluorine. In addition, fluorinations in the liquid phase often proceed more smoothly than those with gaseous fluorine. However, the use of . the interhalogens introduces the problem of separating the uranium hexafluoride from the unreacted reagent and from any by-products which may have been formed. The present work is concerned with the determination of the phase equilibrai among the materials uranium hexafluoride, chlorine trifluoride, and hydrogen fluoride. metal with chlorine trifluoride-hydrogen fluoride solutions or as a result of treating many uranium compounds and ores with chlorine trifluoride. These phase equilibria define the physical conditions necessary for separating the components by the processes of crystallization or distillation and have made possinle the successful Operation of a pilot plant for the direct recovery of uranium hexafluoride from spent metallic uranium fuel elements. (auth)

Bernhardt, H.A.; Barber, E.J.; Davis, W. Jr.; McGill, R.M.

1958-10-31T23:59:59.000Z

294

Iodized Salt  

NLE Websites -- All DOE Office Websites (Extended Search)

Iodized Salt Iodized Salt Name: Theresa Location: N/A Country: N/A Date: N/A Question: Why do they put iodine in salt? Replies: Iodine was introduced into salt at earlier this century when it was discovered that certain areas of the US had a mark deficiency in iodine in the diet of people, and people developed a neck swelling (goiter). The Great Lakes region is one of these areas where the soil is lacking iodine. Goiter can be caused when the thyroid gland swells because of a lack of iodine in the diet. Most medical advise now states that iodine in salt is no longer necessary due to our food sources arising from all over the world. Steve Sample Hi Theresa...see, there are a variety of elements and compounds that are necessary for the proper maintenance of our life. One of these is iodine, since a small quantity of iodine is needed for the adequate functioning of the thyroid gland. A deficiency of iodine produces dire effects, as goiter, where the thyroid gland swollens due to the lack of iodine traces in the diet. The iodine affects directly the tyrhoid gland secretions, which themselves, to a great extent, control heart action, nerve response to stimuli, rate of body growth and metabolism.

295

Stress corrosion cracking of type 304L stainless steel core shroud welds.  

SciTech Connect

Microstructural analyses by advanced metallographic techniques were conducted on mockup welds and a cracked BWR core shroud weld fabricated from Type 304L stainless steel. heat-affected zones of the shroud weld and mockup shielded-metal-arc welds were free of grain-boundary carbide, martensite, delta ferrite, or Cr depletion near grain boundaries. However, as a result of exposure to welding fumes, the heat-affected zones of the welds were significantly contaminated by fluorine and oxygen which migrate to grain boundaries. Significant oxygen contamination promotes fluorine contamination and suppresses classical thermal sensitization, even in Type 304 steels. Results of slow-strain-rate tensile tests indicate that fluorine exacerbates the susceptibility of irradiated steels to intergranular stress corrosion cracking. These observations, combined with previous reports on the strong influence of weld flux, indicate that oxygen and fluorine contamination and fluorine-catalyzed stress corrosion play a major role in cracking of Type 304L stainless steel core shroud welds.

Chung, H. M.; Park, J.-H.; Sanecki, J. E.; Zaluzec, N. J.; Yu, M. S.; Yang, T. T.

1999-10-26T23:59:59.000Z

296

La Roca Blanca de Lhang lhang - Un santuario en Nyag rong  

E-Print Network (OSTI)

de Rag dmar, debido a la progresiva influencia a lo largo de los siglos de la emigración de población mi nyag pa en el Nyag rong, procedentes del norte. La predominancia del dialecto mi nyag habría cambiado el antiguo nombre del área, que era Brag... mi nyag pa shar dang lho phyogs su ‘phos mthus mi nyag log skad da lta’ang lus yod pa de sa gnas ‘dir rag dmar ‘go zer ba ni brag dmar ‘go zer ba yin/ La Roca Blanca de Lhang lhang 15 masculina(dbon brgyud) 9 . Muchos de estos centros religiosos...

Aguillar, Oriol

2007-01-01T23:59:59.000Z

297

New fluorocarbon elastomers for seals for geothermal and other aggressive environments  

DOE Green Energy (OSTI)

Geothermal brines at 600 F which contain metallic salts, H{sub 2}S, and hydrocarbons quickly degrade conventional hydrocarbon elastomers, and hydrolyse crosslinks. Carbon-carbon and carbon-fluorine bonds are expected to be superior, but no such elastomer is now commercially available. We have prepared crosslinked, perfluorocarbon elastomers by radiation crosslinking VDFHFP and TFEP (alternating) copolymers in film and sheet form, and then converting C-H bonds to C-F bonds with elemental Fluorine gas. EPLM elastomers became brittle on fluorination. The best products exceeded 100 days survival at 300 C in simulated geothermal brine. Tensile, elongation, solvent swelling, and TCA methods were used to study the products.

Dumitru, Earl T.; Lagow, R.J.; Kukacka L.E.

1982-10-08T23:59:59.000Z

298

Evaluation and Characterization of Membranes for H2SO4/Water and I2/HI/H2O Water Separation and Hydrogen Permeation for the S-I Cycle  

DOE Green Energy (OSTI)

In this report are the findings into three membrane separation studies for potential application to the Sulfur-Iodine (S-I) thermochemical cycle. The first is the removal of water from hydriodic acid/iodine mixtures. In the S-I cycle, iodine is added to the product of the Bunsen reaction to facilitate the separation of sulfuric acid (H2SO4) from hydriodic acid (HI). The amount of iodine can be as high as 83% of the overall mass load of the Bunsen product stream, which potentially introduces a large burden on the cycle’s efficiency. Removal of water from the HI and iodine mixture would substantially reduce the amount of required additional iodine. In this work, performance data for Nafion® and sulfonated poly (ether ether ketone) (SPEEK) membranes is shown.

Frederick R. Stewart

2006-10-01T23:59:59.000Z

299

Activated carbon material  

DOE Patents (OSTI)

Activated carbon particles for use as iodine trapping material are impregnated with a mixture of selected iodine and potassium compounds to improve the iodine retention properties of the carbon. The I/K ratio is maintained at less than about 1 and the pH is maintained at above about 8.0. The iodine retention of activated carbon previously treated with or coimpregnated with triethylenediamine can also be improved by this technique. Suitable flame retardants can be added to raise the ignition temperature of the carbon to acceptable standards.

Evans, A. Gary (North Augusta, SC)

1978-01-01T23:59:59.000Z

300

Available Technologies: Rotenone Analogs: High Extraction and ...  

Fusion : Iodine-123 rotenone SPECT/CT images of canine heart. STATUS: Published Patent Application WO/2008/133730 available at http://www.wipo.int and ...

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


301

Nanoporous Al2O3 as a “Getter” for Volatile Radionuclides ...  

The first phase of this project is capture and encapsulation which is achieved by using nanoporous alumina to confine gaseous iodine, for example, ...

302

Technologic Papers 1914  

Science Conference Proceedings (OSTI)

... Industrial gas calorimetry, T 36, Waidner, CW; Mueller, EF http://dx.doi.org/ 10.6028/nbst.1914. Iodine number of linseed and petroleum oils, T 37 ...

2013-03-21T23:59:59.000Z

303

Conditioning of Iodate Ion in an Apatite-Like Ceramic  

Science Conference Proceedings (OSTI)

Concerning the conditioning of Iodine, one promising approach consists in ... Removal of Xenon and Krypton from Air Using Metal Organic Frameworks.

304

Effect of excess iodide on thyroid function of rainbow trout ...  

Science Conference Proceedings (OSTI)

Fish Physiology and Biochemistry vol. ... iodine metabolism appear to exist between mammals and fish. ... The plasma iodide levels of teleost fish in general, .

305

Analytical Data Report of Water Samples Collected For I-129 Analysis  

SciTech Connect

This is an analytical data report for samples received from the central plateau contractor. The samples were analyzed for iodine-129.

Lindberg, Michael J.

2009-10-26T23:59:59.000Z

306

CX-010652: Categorical Exclusion Determination | Department of...  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Categorical Exclusion Determination CX-010652: Categorical Exclusion Determination "Technetium and Iodine Removal Studies with SuperLig Resin CX(s) Applied: B3.6 Date: 06262013...

307

Page not found | Department of Energy  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

the State of Washington a limited amount of discovery pertaining to iodine-129, technetium-99, and... http:energy.govemdownloadsreport-review-hanford-solid-waste-environm...

308

Grouting project to protect Snake River Plain Aquifer completed...  

NLE Websites -- All DOE Office Websites (Extended Search)

Treated locations contain waste contaminated with mobile forms of the radionuclides technetium-99 and iodine-129 produced during historical operations at the DOEs Idaho Site....

309

Report of the Review of the Hanford Solid Waste Environmental...  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

the State of Washington a limited amount of discovery pertaining to iodine-129, technetium-99, and groundwater analyses. While compiling information to respond to the State...

310

Office of Human Radiation Experiments - Archived Website  

NLE Websites -- All DOE Office Websites (Extended Search)

documents cold war metabolism of lethal dose studies with rates dose experiments medical research program Iodine-131 Iron-59 For further information regarding information...

311

Measure of precursor electron density profiles of laser launched radiative shocks  

E-Print Network (OSTI)

We have studied the dynamics of strong radiative shocks generated with the high-energy subnanosecond iodine laser at Prague Asterix Laser System facility

Busquet, Michel; González, Matthias; Audit, Edouard; 10.1063/1.3330636

2010-01-01T23:59:59.000Z

312

Iosil Energy Corporation | Open Energy Information  

Open Energy Info (EERE)

Corporation Place Winter Park, Florida Zip FL 32789 Product Florida iodine-based silicon production technology developer. References Iosil Energy Corporation1 LinkedIn...

313

Nitrene transfer reactions by late transition metal complexes  

E-Print Network (OSTI)

This thesis presents nitrene transfer reactions that are catalyzed or mediated by late transition metal complexes. Sterically large, fluorinated supporting ligands are used to minimize potential side reactions. A new ...

Hamilton, Charles W., Ph. D. Massachusetts Institute of Technology

2007-01-01T23:59:59.000Z

314

Method of Disposing of Corrosive Gases  

DOE Patents (OSTI)

Waste gas containing elemental fluorine is disposed of in the disclosed method by introducing the gas near the top of a vertical chamber under a downward spray of caustic soda solution which contains a small amount of sodium sulfide.

Burford, W.B. III; Anderson, H.C.

1950-07-11T23:59:59.000Z

315

SYSTEM FOR CONVERSION OF UF$sub 4$ TO UF$sub 6$  

DOE Patents (OSTI)

Method and apparatus are presented for rapid and complete conversion of solid, powdered uranium tetrafiuorlde to uranlum hexafluorlde by treating the UF/ sub 4/ with fluorine gas at a temperature of about 800 icient laborato C.

Brater, D.G.; Pike, J.W.

1958-12-01T23:59:59.000Z

316

OLEFINIC CHLOROFLUOROCARBON (OCFC) FIRE ...  

Science Conference Proceedings (OSTI)

... J. - An. Chem.Soc. (1957), 79, 4981-4982. (23) Simons, J. H. "Fluorine Chernisy-y", Vol I1 (Academic Press, inc., Kew York, 1954), page 219. ...

2011-10-11T23:59:59.000Z

317

CROSSED MOLECULAR BEAM STUDIES OF UN-IMOLECULAR REACTION DYNAMICS  

E-Print Network (OSTI)

released in carbon-chlorine bond formation to redistributeIn the reaction of chlorine and fluorine atoms with vinylthe reaction of The reaction chlorine atoms with 1, 2 and 3-

Buss, R.J.

2010-01-01T23:59:59.000Z

318

MOLECULAR BEAM STUDIES OF UNIMOLECULAR REACTIONS: Cl, F + C2H3Br  

E-Print Network (OSTI)

pro~ of fluorine and chlorine atoms with vinyl bromide areheated nickle oven at The chlorine source was similar,the tot&l energy for the chlorine re&ction &nd FWHM ~ 4.2 kJ

Buss, Richard J.

2011-01-01T23:59:59.000Z

319

Argonne CNM: Nanofabrication and Devices Capabilities  

NLE Websites -- All DOE Office Websites (Extended Search)

PECVD System for CNT and Graphene Synthesis Dry Etching RIE Oxford PlasmaLab 100, Chlorine Chamber RIE Oxford PlasmaLab 100, Fluorine Chamber RIE March CS-1701, Chlorine...

320

BONDING IN INORGANIC COMPOUNDS: A STUDY BY X-RAY PHOTOELECTRON SPECTROSCOPY  

E-Print Network (OSTI)

to calculate the fluorine and chlorine charges in CIF. C IfEB=248.62eV ) for Ref. 2. Chlorine binding energies arefor Ref. 2, 3, & 4; the chlorine values for Ref. 1 are based

Avanzino, Steven Charles

2011-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


321

Superhydrophobic/Superhydrophilic Switchable Wettability on ...  

Science Conference Proceedings (OSTI)

... and subsequent coating of photosensitive fluorinated azobenzene molecules, we can ... Extended-Chain Crystals of High-Pressure Crystallized Poly (Ethylene ... Wood/Polypropylene Composites Parts with Ultrasonic Oscillation Assistant.

322

Modeling the micellization behavior of fluorosurfactants using molecular-thermodynamic theory  

E-Print Network (OSTI)

Fluorinated surfactants are an important class of surfactants because they possess properties that are far superior than those of their hydrocarbon analogs. As a result, they are used in a wide variety of applications ...

Iyer, Jaisree (Jaisree Kannan)

2013-01-01T23:59:59.000Z

323

Liquid-phase and vapor-phase dehydration of organic/water solutions  

DOE Patents (OSTI)

Processes for dehydrating an organic/water solution by pervaporation or vapor separation using fluorinated membranes. The processes are particularly useful for treating mixtures containing light organic components, such as ethanol, isopropanol or acetic acid.

Huang, Yu (Palo Alto, CA); Ly, Jennifer (San Jose, CA); Aldajani, Tiem (San Jose, CA); Baker, Richard W. (Palo Alto, CA)

2011-08-23T23:59:59.000Z

324

Available Technologies: Stable and Highly Conductive ...  

The fluorine insertion led to at least a 40X increase in the conductivity of stoichiometric TiO2 and a 3X increase in the rectification factor of TiO2 on p-type ...

325

Fuel cell electrolyte membrane with acidic polymer  

DOE Patents (OSTI)

An electrolyte membrane is formed by an acidic polymer and a low-volatility acid that is fluorinated, substantially free of basic groups, and is either oligomeric or non-polymeric.

Hamrock, Steven J. (Stillwater, MN); Larson, James M. (Saint Paul, MN); Pham, Phat T. (Little Canada, MN); Frey, Matthew H. (Cottage Grove, MN); Haugen, Gregory M. (Edina, MN); Lamanna, William M. (Stillwater, MN)

2009-04-14T23:59:59.000Z

326

The Standards Actions, April 1996  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Titration (Ref. Z6053Z). * New Standard, Test Method for Total Fluorine in Coal and Coke by the Pyrohydrolytic Extraction and the Ion Selec- tive Electrode or Ion Chromatograph...

327

VOLATILE FLUORIDE PROCESS FOR SEPARATING PLUTONIUM FROM OTHER MATERIALS  

DOE Patents (OSTI)

The separation of plutonium from uranium and/or tission products by formation of the higher fluorides of uranium and/or plutonium is discussed. Neutronirradiated uranium metal is first convcrted to the hydride. This hydrided product is then treatced with fluorine at about 315 deg C to form and volatilize UF/sup 6/ leaving plutonium behind. The plutonium may then be separated by reacting the residue with fluorine at about 500 deg C and collecting the volatile plutonium fluoride thus formed.

Spedding, F.H.; Newton, A.S.

1959-04-14T23:59:59.000Z

328

VOLATILE FLUORIDE PROCESS FOR SEPARATING PLUTONIUM FROM OTHER MATERIALS  

DOE Patents (OSTI)

The separation of plutonium from uranium and/or fission products by formation of the higher fluorides off uranium and/or plutonium is described. Neutronirradiated uranium metal is first converted to the hydride. This hydrided product is then treated with fluorine at about 315 deg C to form and volatilize UF/sub 6/ leaving plutonium behind. Thc plutonium may then be separated by reacting the residue with fluorine at about 5004DEC and collecting the volatile plutonium fluoride thus formed.

Spedding, F.H.; Newton, A.S.

1959-04-14T23:59:59.000Z

329

Modified lithium vanadium oxide electrode materials products and methods  

DOE Patents (OSTI)

A method of improving certain vanadium oxide formulations is presented. The method concerns fluorine doping formulations having a nominal formula of LiV.sub.3 O.sub.8. Preferred average formulations are provided wherein the average oxidation state of the vanadium is at least 4.6. Herein preferred fluorine doped vanadium oxide materials, electrodes using such materials, and batteries including at least one electrode therein comprising such materials are provided.

Thackeray, Michael M. (Naperville, IL); Kahaian, Arthur J. (Chicago, IL); Visser, Donald R. (Naperville, IL); Dees, Dennis W. (Downers Grove, IL); Benedek, Roy (Western Springs, IL)

1999-12-21T23:59:59.000Z

330

Rare Earth Oxide Fluoride Nanoparticles And Hydrothermal Method For Forming Nanoparticles  

DOE Patents (OSTI)

A hydrothermal method for forming nanoparticles of a rare earth element, oxygen and fluorine has been discovered. Nanoparticles comprising a rare earth element, oxygen and fluorine are also described. These nanoparticles can exhibit excellent refractory properties as well as remarkable stability in hydrothermal conditions. The nanoparticles can exhibit excellent properties for numerous applications including fiber reinforcement of ceramic composites, catalyst supports, and corrosion resistant coatings for high-temperature aqueous solutions.

Fulton, John L. (Richland, WA); Hoffmann, Markus M. (Richland, WA)

2003-12-23T23:59:59.000Z

331

PREPARATION OF URANIUM HEXAFLUORIDE  

DOE Patents (OSTI)

A process is described for preparing uranium hexafluoride from carbonate- leach uranium ore concentrate. The briquetted, crushed, and screened concentrate is reacted with hydrogen fluoride in a fluidized bed, and the uranium tetrafluoride formed is mixed with a solid diluent, such as calcium fluoride. This mixture is fluorinated with fluorine and an inert diluent gas, also in a fluidized bed, and the uranium hexafluoride obtained is finally purified by fractional distillation.

Lawroski, S.; Jonke, A.A.; Steunenberg, R.K.

1959-10-01T23:59:59.000Z

332

New fluorocarbon elastomers for seals for geothermal and other aggressive environments. Final report  

DOE Green Energy (OSTI)

Saturated ethyllenic elastomers having a range of methyl group substitution, and a range of partial fluorine substitution were screened. Elastomers based on vinylidene fluoride hexafluoropropylene (VDFHFP) and those based on tetrafluoroethylenepropylene (TFEP) (alternating) were successfully cross-linked by electron-beam radiation and fluorinated to yield elastomeric products, but those based on ethylene-propylene-diene (EPDM) elastomer became brittle after fluorination. The best products were evaluated using tensile strength, elongation at break, solvent swelling, thermogravimetric analysis and infrared. A wide range of carbon-black filled compositions using the TFEP elastomer were cross-linked. The compositions were then fluorinated at or near room temperature for extended periods of time. After fluorination the samples were subjected to geothermal brine at 300/sup 0/C. The best carbon-black filled composition again lasted at least 100 days in the geothermal brine. This filler-elastomer composition was chosen for use in the production of 0-rings. The 0-rings were produced by compression molding using a 30 ton hydraulic press. Various sizes of 0-rings were produced ranging fro 0.8 to 2.0 inches in diameter and from 1/16 to 3/16 inches in width. The final 0-rings were cross-linked at 40 Mrad and fluorinated under the optimized conditions developed for the samples.

Lagow, R.J.

1982-12-01T23:59:59.000Z

333

Method and means of monitoring the effluent from nuclear facilities  

DOE Patents (OSTI)

Radioactive iodine is detected in the effluent cooling gas from a nuclear reactor or nuclear facility by passing the effluent gas through a continuously moving adsorbent filter material which is then purged of noble gases and conveyed continuously to a detector of radioactivity. The purging operation has little or no effect upon the concentration of radioactive iodine which is adsorbed on the filter material.

Lattin, Kenneth R. (Richland, WA); Erickson, Gerald L. (Richland, WA)

1976-01-01T23:59:59.000Z

334

Physics of Hot Partonic Matter at LHC-ALICE  

SciTech Connect

The field of high energy nuclear physics has recently reached epoch making discoveries at the Relativistic Heavy Ton Collider at Brookhaven National Laboratory, highlighted with that of new state of nuclear matter with partonic degrees of freedom. The ALICE experiment at the Large Hadron Collider at CERN aims at comprehensive investigation and understanding of properties of the hot and dense partonic matter, as the only experiment dedicated to nucleus-nucleus collisions at the facility. Physics prospects at ALICE are reviewed including jet quenching as a probe of energy loss of quarks in the created medium, direct and thermal photons as vital probes of the thermal properties, and quarkonia as a beloved probe of color deconfinement, along with latest status of the detector systems including the high resolution electromagnetic calorimeter, PHOS, and a quick report from the first operation of LHC and ALICE in December, 2009.

Shigaki, K. [Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8526 (Japan)

2010-06-01T23:59:59.000Z

335

elementwordsearch_2001  

NLE Websites -- All DOE Office Websites (Extended Search)

C C I D L A B I R A G I K P O T A S S I U M B C N I Z I C N S R X Z R C L N I U M D A E L P I T I A O O H O O X Y O U I M O D A R B F Z T I R A D R E L D M P U N R X C P Y A A I C I B C K G O L D E I T G R Y Y H L I D B V I O D O X O B I M P A O N E A G L U V I Y E N A Z N I L Y U K E L N M L N I O T A U L X Y C I I O M O M E R C U R Y U R R O N M O Y N K M U N I T A L P V I R M N O I N O I N H O L C M G K A R F P I S M U I O N I V L I Y M N I T R O G E N L T O U T I X E U A O R D I I I T K O S H M U I D A L L A P N O D A R T I B I H L Y T A T U I V A F R R S D F S O N C A L C I U M G O R U O R R U R H E L U G A L U M I N U M N N A M R G A R R E L U R E W A R G D O E M E I N L L O N A N R E O O N I O D E R N R S D U I R B N K L I I N R H Z R A G S I R E E R M U C N W E N A D N I P A P E K D P U V N O M M N E T S G N U T N S H N V O I S I L V E R E I N N E L Y R I E O A N I C K E L I M U I N A T I T O T X S F H X S I L I C O N S W O D A H S R E P P O C P Y ALUMINUM GOLD NICKEL SILICON ANTIMONY HELIUM NITROGEN SILVER ARGON HYDROGEN OXYGEN SODIUM BERYLLIUM IODINE PALLADIUM SULFUR BORON IRON PHOSPHORUS TIN CALCIUM KRYPTON PLATINUM TITANIUM CARBON LEAD PLUTONIUM TUNGSTEN CHLORINE LITHIUM POTASSIUM URANIUM COPPER MERCURY RADIUM ZINC FLUORINE NEON RADON ZIRCONIUM

336

Stress corrosion cracking of austenitic stainless steel core internal welds.  

SciTech Connect

Microstructural analyses by several advanced metallographic techniques were conducted on austenitic stainless steel mockup and core shroud welds that had cracked in boiling water reactors. Contrary to previous beliefs, heat-affected zones of the cracked Type 304L, as well as 304 SS core shroud welds and mockup shielded-metal-arc welds, were free of grain-boundary carbides, which shows that core shroud failure cannot be explained by classical intergranular stress corrosion cracking. Neither martensite nor delta-ferrite films were present on the grain boundaries. However, as a result of exposure to welding fumes, the heat-affected zones of the core shroud welds were significantly contaminated by oxygen and fluorine, which migrate to grain boundaries. Significant oxygen contamination seems to promote fluorine contamination and suppress thermal sensitization. Results of slow-strain-rate tensile tests also indicate that fluorine exacerbates the susceptibility of irradiated steels to intergranular stress corrosion cracking. These observations, combined with previous reports on the strong influence of weld flux, indicate that oxygen and fluorine contamination and fluorine-catalyzed stress corrosion play a major role in cracking of core shroud welds.

Chung, H. M.; Park, J.-H.; Ruther, W. E.; Sanecki, J. E.; Strain, R. V.; Zaluzec, N. J.

1999-04-14T23:59:59.000Z

337

U.S. Transparency monitoring under the U.S./Russian HEU purchase agreement  

SciTech Connect

The conversion of Highly Enriched Uranium (HEU) metal to low enriched uranium (LEU) takes place at four Russian sites. HEU metal to oxide processing began in 1994 with shipments of HEU oxide from the Siberian Chemical Enterprise (SChE) to the Ural Electrochemical Integrated Plant (UEIP) fluorination and blending facility. U.S. transparency monitoring at these facilities began in February 1996. In 1996, fluorination and blending operations began at the Electrochemical Plant (ECP). In 1997, additional HEU metal to oxide was added at the Mayak Production Association (MPA), and additional fluorination and blending operations have been performed at SChE. U.S. transparency monitoring at these facilities is intended to provide confidence that HEU weapons components are received, that the HEU metal is converted to HEU oxide, and that the HEU is blended to LEU prior to shipment to the U.S. Enrichment Corporation (USEC). The monitoring begins with observation of HEU weapon components in sealed containers, including confirmation of the {sup 235}U enrichment using U.S. nondestructive assay (NDA) equipment. The feeding of HEU metal shavings to the oxidation process and the subsequent packaging of the HEU oxide for shipment to the fluorination and blending facilities are then monitored. At those facilities, monitors are allowed to witness the fluorination and blending of the HEU into LEU. Monitors are allowed to use the NDA instrumentation to confirm that HEU is being processed. A series of process and material accountancy documents are provided to U.S. monitors.

Benton, J; Dougherth, D R; Glaser, J W; Thomas, D C

1999-07-27T23:59:59.000Z

338

Confinement of airborne radioactivity. Progress report, January--December 1974  

SciTech Connect

Several commercial activated carbons, marketed for iodine removal in reactor off-gas cleanup systems, were evaluated for iodine penetration at elevated temperatures (4 hr at 180$sup 0$C), and the penetration data varied widely. Subsequent chemical analysis of the samples indicated a strong correlation between the atom ratio of iodine to potassium (I/K) in the carbon and the high-temperature performance data. Iodine penetration tests were also performed on several carbons in an intense gamma radiation field (greater than 10$sup 7$ rads/hr). Test data show that carbons intentionally exposed to high concentrations of DOP aerosol performed as well as unexposed carbons. Studies of the rate of evaporation of elemental iodine from aqueous solutions indicated that significant quantities of I$sub 2$ might be expected to become airborne within a short period of time (5 hr) after release to open ponds. Addition of sodium thiosulfate to the solution substantially reduced the evaporative loss of iodine; however, the effects of high-intensity radiation fields on iodine-thiosulfate solutions remain to be evaluated. Small HEPA filters containing filter media of the type used in the Savannah River confinement system were exposed to reactor building air and a high-intensity radiation field. Following this exposure, they were tested for flow performance under simulated accident conditions. Radiation exposure slightly impaired the performance of new filters and improved the performance of service-aged filters. Service aging effects on filter performance were far more significant than radiation effects. (auth)

Dexter, A.H.; Evans, A.G.; Jones, L.R.

1974-01-01T23:59:59.000Z

339

It's Elemental - The Element Neon  

NLE Websites -- All DOE Office Websites (Extended Search)

Fluorine Fluorine Previous Element (Fluorine) The Periodic Table of Elements Next Element (Sodium) Sodium The Element Neon [Click for Isotope Data] 10 Ne Neon 20.1797 Atomic Number: 10 Atomic Weight: 20.1797 Melting Point: 24.56 K (-248.59°C or -415.46°F) Boiling Point: 27.07 K (-246.08°C or -410.94°F) Density: 0.0008999 grams per cubic centimeter Phase at Room Temperature: Gas Element Classification: Non-metal Period Number: 2 Group Number: 18 Group Name: Noble Gas What's in a name? From the Greek word for new, neos. Say what? Neon is pronounced as NEE-on. History and Uses: Neon was discovered by Sir William Ramsay, a Scottish chemist, and Morris M. Travers, an English chemist, shortly after their discovery of the element krypton in 1898. Like krypton, neon was discovered through the

340

It's Elemental - Isotopes of the Element Neon  

NLE Websites -- All DOE Office Websites (Extended Search)

Fluorine Fluorine Previous Element (Fluorine) The Periodic Table of Elements Next Element (Sodium) Sodium Isotopes of the Element Neon [Click for Main Data] Most of the isotope data on this site has been obtained from the National Nuclear Data Center. Please visit their site for more information. Naturally Occurring Isotopes Mass Number Natural Abundance Half-life 20 90.48% STABLE 21 0.27% STABLE 22 9.25% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 16 9×10-21 seconds Double Proton Emission 100.00% 17 109.2 milliseconds Electron Capture with delayed Alpha Decay No Data Available Electron Capture 100.00% Electron Capture with delayed Proton Emission 100.00% 18 1.6670 seconds Electron Capture 100.00% 19 17.22 seconds Electron Capture 100.00% 20 STABLE - -

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


341

Novel silane and disilane precursors to amorphous semiconductors: Final subcontract report, May 1988  

DOE Green Energy (OSTI)

This Final Report describes the preparation and characterization of amorphous fluorohydrogenated silicon thin films. The novel approach in this study lies in the use of fluorinated silanes as film precursors. The advantages of this method are well defined initial ratios of hydrogen and fluorine to silicon and greatly reduced hazards in the handling of the gas. Fluorine derivatives of both silane and disilane were synthesized. Both glow discharge (or plasma-enhanced CVD) and thermal (CVD) methods were employed to prepare amorphous silicon on glass and silicon wafers. The electrical characterization of the material prepared from difluorosilane showed that the a-Si:H:F films obtained are of solar-grade semiconductor quality and can be doped to p- and n-type materials with diborane and phosphine. 29 refs., 24 figs., 10 tabs.

Pernisz, U.C.; Sharp, K.G.

1988-09-01T23:59:59.000Z

342

Novel silane and disilane precursors to amorphous semiconductors. Annual report, 1 April 1985-31 March 1986  

SciTech Connect

This report describes the preparation and characterization of amorphous fluorohydrogenated silicon thin films. The novel approach lies in the use of fluorinated silanes as film precursors. This method has the advantages of well-defined initial ratios of hydrogen and fluorine and a greatly reduced hazards in the handling of the gas. Fluorine derivatives of both silane and disilane were synthesized. A conventional method, glow discharge (or plasma-enhanced chemical vapor deposition), was employed to prepare amorphous silicon on glass and Si wafers. The electrical characterization of the material prepared from difluorosilane (the main precursor during the contract period covered in this report) showed that the a-Si:H:F films obtained are of solar-grade semiconductor quality and can be doped to p- and n-type material with diborane and phosphine.

Pernisz, U.; Sharp, K.

1986-08-01T23:59:59.000Z

343

CX-007967: Categorical Exclusion Determination | Department of Energy  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

67: Categorical Exclusion Determination 67: Categorical Exclusion Determination CX-007967: Categorical Exclusion Determination "Electrochemical Fluorination in Molten Fluoride Salts CX(s) Applied: B3.6 Date: 02/07/2012 Location(s): South Carolina Offices(s): Savannah River Operations Office This EEC covers activities related to development of an electrochemical fluorination process to separate selected metals (non-RCRA) from depleted uranium. The goal of the process is to convert depleted uranium metal (U) to gaseous uranium hexafluoride (UF6) that can be easily separated from solution while other metallic constituents remain as metals or are converted to non-volatile fluoride salts. The electrochemical fluorination process will be conducted in molten fluoride eutectic salts at temperatures

344

Optimization of transparent and reflecting electrodes for amorphous silicon solar cells. Final technical report  

DOE Green Energy (OSTI)

Transparent conducting fluorine doped zinc oxide was deposited as thin films on soda lime glass substrates by atmospheric pressure chemical vapor deposition (CVD) at substrate temperatures of 460 to 500 degrees C. The precursors diethylzinc, tetramethylethylenediamine and benzoyl fluoride were dissolved in xylene. This solution was nebulized ultrasonically and then flash vaporized by a carrier gas of nitrogen preheated to 150 degrees C. Ethanol was vaporized separately, and these vapors were then mixed to form a homogeneous vapor mixture. Good reproducibility was achieved using this new CVD method. Uniform thicknesses were obtained by moving the heated glass substrates through the deposition zone. The best electrically and optical properties were obtained when the precursor solution was aged for more than a week before use. The films were polycrystalline and highly oriented with the c-axis perpendicular to the substrate. More than 90% of the incorporated fluorine atoms were electrically active as n-type dopants. The electrical resistivity of the films was as low as 5 x 10/sup -4/ Omega cm. The mobility was about 45 cm ²/Vs. The electron concentration was up to 3 x 10 %sup20;/cm³. The optical absorption of the films was about 3-4% at a sheet resistance of 7 ohms/square. The diffuse transmittance was about 10% at a wavelength of 650 nm. Amorphous ilicon solar cells were deposited using the textured fluorine doped zinc oxide films as a front electrode. The short circuit current was increased over similar cells made with fluorine doped tin oxide, but the open circuit voltages and fill factors were reduced. The voltage was restored by overcoating the fluorine-doped zinc oxide with a thin layer of fluorine-doped tin oxide.

Gordon, R.G.; Kramer, K.; Liang, H.; Liu, X.; Pang, D.; Teff, D.

1998-09-01T23:59:59.000Z

345

Supercritical fluid extraction  

DOE Patents (OSTI)

A method of extracting metalloid and metal species from a solid or liquid material by exposing the material to a supercritical fluid solvent containing a chelating agent. The chelating agent forms chelates that are soluble in the supercritical fluid to allow removal of the species from the material. In preferred embodiments, the extraction solvent is supercritical carbon dioxide and the chelating agent is a fluorinated or lipophilic crown ether or fluorinated dithiocarbamate. The method provides an environmentally benign process for removing contaminants from industrial waste without using acids or biologically harmful solvents. The chelate and supercritical fluid can be regenerated, and the contaminant species recovered, to provide an economic, efficient process.

Wai, Chien M. (Moscow, ID); Laintz, Kenneth (Pullman, WA)

1994-01-01T23:59:59.000Z

346

Vacuum ultraviolet laser  

SciTech Connect

Transitions from the 2p.sup.4 (.sup.1 S.sub.0)3s .sup.2 S.sub.1/2 state of atomic fluorine to all allowed lower states produces laser emission at six new wavelengths: 680.7 .ANG., 682.6 .ANG., 3592.7 .ANG., 3574.1 .ANG., 6089.2 .ANG., and 6046.8 .ANG.. Coherent radiation at these new wavelengths can be generated in an atomic fluorine laser operated as an amplifier or as an oscillator.

Berkowitz, Joseph (Hinsdale, IL); Ruscic, Branko M. (Zagreb, YU); Greene, John P. (Woodridge, IL)

1986-01-01T23:59:59.000Z

347

Vacuum ultraviolet laser  

DOE Patents (OSTI)

Transitions from the 2p/sup 4/(/sup 1/S/sub 0/)3s /sup 2/S/sub 1/2/ state of atomic fluorine to all allowed loser states produces laser emission at six new wavelengths: 680.7A, 682.6A, 3592.7A, 3574.1A, 6089.2A, and 6046.8A. Coherent radiation at these new wavelengths can be generated in an atomic fluorine laser operated as an amplifier or as an oscillator.

Berkowitz, J.; Ruscic, B.M.; Greene, J.P.

1984-07-06T23:59:59.000Z

348

Edible Fat Laboratory Proficiency Testing Program  

Science Conference Proceedings (OSTI)

Lab Proficiency Testing for Edible Fat to test OSI,FFA, AOCS Color, Capillary Melting Point, Iodine Value, Lovibond Color, Mettler Dropping Point, a;-Monoglycerides, SFC Edible Fat Laboratory Proficiency Testing Program Laboratory Proficiency Program (LPP

349

Gas Chromatography Laboratory Proficiency Testing Program  

Science Conference Proceedings (OSTI)

Lab Proficiency Testing provider for Gas Chromatography to determine Fatty Acid Composition and Iodine Value using AOCS methods Ce 1-62 and Cd 1c-85. Gas Chromatography Laboratory Proficiency Testing Program Laboratory Proficiency Program (LPP) aocs appl

350

Marine Products and Marine Oil Laboratory Proficiency Testing Program  

Science Conference Proceedings (OSTI)

Lab Proficiency Testing service for Marine Products and Marine Oil samples to test Anisidine Value, Free Fatty Acid, Iodine Value, Insoluble Impurities, Moisture, Peroxide Value. Marine Products and Marine Oil Laboratory Proficiency Testing Program Labo

351

AOCS Official Method Cd 1b-87  

Science Conference Proceedings (OSTI)

Iodine Value of Fats and Oils Cyclohexane Method AOCS Official Method Cd 1b-87 Methods and Analyses acid agricultural analysis analytical analytical chemistry analytical methods aocs aocs methods april articles biotechnology certified chemists chloroprop

352

Materials Issues in Nuclear Waste Management in the 21st Century  

Science Conference Proceedings (OSTI)

Scope, While nuclear energy might provide a solution to the increasing demand ... using experiments, theory, mathematical and physical modeling, and simulation. ... Adsorption of of Radioactive Iodine from Used Nuclear Fuel Reprocessing ...

353

Depletion, quantum jumps, and temperature measurements of ??Sr? ions in a linear Paul Trap  

E-Print Network (OSTI)

This thesis describes the design and construction of two laser systems to probe the 674nm transition of ??Sr? ions in a linear Paul trap. The first laser system made use of a molecular transition in Iodine to stabilize the ...

Richerme, Philip J

2006-01-01T23:59:59.000Z

354

Microsoft Word - Transportation pdf.doc  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Finnish homes 0.23 to 0.86 Christensen and Mustonen, 1987 Various radioisotopes Danish home 0.1 to 0.5 Roed and Cannell, 1987 Noble gGases, methyl iodide, elemental iodine,...

355

ORISE: REAC/TS Radiation Treatment Medications  

NLE Websites -- All DOE Office Websites (Extended Search)

air during a radiation event and then inhaled, it is quickly absorbed by the thyroid gland and can cause damage. KI acts to block the radioactive iodine from being taken into...

356

AOCS Official Method Tg 1a-64 (Pending)  

Science Conference Proceedings (OSTI)

Iodine Value of Fatty Acids, Wijs Method AOCS Official Method Tg 1a-64 (Pending) Methods Downloads Methods Downloads Official Methods and Recommended Practices of the AOCS (Methods) aocs applicants certified chemist chemists fats lab laboratorie

357

AOCS Official Method Cd 1b-87 (Pending)  

Science Conference Proceedings (OSTI)

Iodine Value of Fats and Oils Cyclohexane Method AOCS Official Method Cd 1b-87 (Pending) Methods Downloads Methods Downloads Official Methods and Recommended Practices of the AOCS (Methods) aocs applicants certified chemist chemists fats lab lab

358

Perspective on the Role of Negative Ions and Ion-Ion Plasmas in Heavy Ion Fusion Science, Magnetic Fusion Energy, and Related Fields  

E-Print Network (OSTI)

of positive and negative chlorine ions, with only a smalltest case. We chose chlorine because, unlike iodine orTwo sets of experiments with chlorine using different RF ion

Kwan, J.W.

2008-01-01T23:59:59.000Z

359

Perspective on the Role of Negative Ions and Ion-Ion Plasmas in Heavy Ion Fusion Science, Magnetic Fusion Energy, and Related Fields  

E-Print Network (OSTI)

pos itive and ne gative chlorine i ons, w ith onl y a s malltest case. W e ch ose chlorine b ecause, u nlike iodine o rsets of e xperiments with chlorine using different RF ion s

Grisham, L. R.

2010-01-01T23:59:59.000Z

360

MATERIALS AND MOLECULAR RESEARCH DIVISION, ANNUAL REPORT 1976  

E-Print Network (OSTI)

coordinated ionic site for the chlorine atom on the siliconK to produce beams of chlorine, bromine, or iodine moleculesPeak flux velocities for chlorine atoms chlorine molecules

Authors, Various

2010-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


361

Origin of Halogens and Nitrogen in Enstatite Chondrites  

E-Print Network (OSTI)

D.Y. Je rome, Abundances of chlorine, bromine and iodine inof boron, lithium and chlorine in meteorites, in MeteoriteW. Scherle, Determination of chlorine in stony meteorites by

Rubin, Alan E.; Choi, Byeon-Gak

2009-01-01T23:59:59.000Z

362

AOCS Official Method Cd 1e-01  

Science Conference Proceedings (OSTI)

Determination of Iodine Value by Pre-calibrated FT-NIR with Disposable Vials AOCS Official Method Cd 1e-01 Methods Methods and Analyses Analytical Chemistry Methods Downloads Methods Downloads DEFINITION The me

363

Initial Assessment of the Consolidation of Chalcogels into a Viable Waste Form  

SciTech Connect

This report provides some preliminary data for the consolidation of chalcogen-based aerogels. The chalcogels tested to date at PNNL show great promise as iodine sorbents and preliminary consolidation research shows that they can be melted into a phase-pure glass at moderate temperatures. The preliminary consolidation experiments show that these materials might attack fused quartz so an alternative crucible material will likely need to be used to prevent this. The next steps will be to • Consider melting other chalcogel chemistries, e.g., Sn-Sb-S, Ge-Sn-S chalcogels • Consider melting chalcogels with adsorbed iodine to monitor iodine loss during melting • Optimize the consolidation temperatures to minimize the iodine loss and volatilization

Riley, Brian J.; Lepry, William C.

2012-08-31T23:59:59.000Z

364

Categorical Exclusion Determinations: South Carolina | Department...  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Technology Laboratory June 26, 2013 CX-010652: Categorical Exclusion Determination Technetium and Iodine Removal Studies with SuperLig Resin CX(s) Applied: B3.6 Date: 06262013...

365

U.S. Department of Energy Categorical Exclusion ...  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Technetium and Iodine Removal Studies with SuperLig Resin Savannah River Site AikenAikenSouth Carolina An ion exchange resin, SuperLig 639 by IBC Advanced Technologies, is to be...

366

Page not found | Department of Energy  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

ical-exclusion-determination Download CX-010652: Categorical Exclusion Determination Technetium and Iodine Removal Studies with SuperLig Resin CX(s) Applied: B3.6 Date: 06262013...

367

AOCS Official Method Tg 1-64 (Pending)  

Science Conference Proceedings (OSTI)

Iodine Value, Wijs Method AOCS Official Method Tg 1-64 (Pending) Methods Downloads Methods Downloads Official Methods and Recommended Practices of the AOCS (Methods) aocs applicants certified chemist chemists fats lab laboratories laboratory lip

368

Zinc-Column Hydride Generation and 7'rapping Dilute standards or samples containing less than 5 mg  

E-Print Network (OSTI)

- sium iodide-iodine trapping solution in the centrifuge tube. The nitrogen gas flow rate wasadjusted furnace program (Table I). Gas flow was stopped during the atomizationstep. TABLE I Optimized Furnace

Canberra, University of

369

MEASUREMENT OF RADIOIODINE IN PUREX STACK GASES  

SciTech Connect

The chemical behavior of iodine-131 in stack air from this site's Purex process is reported. The radioiodine in the stack gases apparently consists of variable proportions of molecular vapor and other forms of iodine, thus causing the efficiencies for most collection media to vary widely. Activated charcoal is a satisfactory collection medium although Process gases (ammonia and oxides of nitrogen) lower the efficiency of the charcoal from 99 to 88%. Ambient temperature and humidity had no effect on deposition and retention of iodine in long stainless steel sampling lines. Process conditions did have an effect and estimates of iodine released were 10 to 15% low due to this line loss. (auth)

Jacobsen, W.R.; Jolly, L. Jr.

1963-05-01T23:59:59.000Z

370

Exploding conducting film laser pumping apparatus  

DOE Patents (OSTI)

The 342-nm molecular iodine and the 1.315-..mu..m atomic iodine lasers have been optically pumped by intense light from exploding-metal-film discharges. Brightness temperatures for the exploding-film discharges were approximately 25,000 K. Although lower output energies were achieved for such discharges when compared to exploding-wire techniques, the larger surface area and smaller inductance inherent in the exploding-film should lead to improved efficiency for optically-pumped gas lasers.

Ware, K.D.; Jones, C.R.

1984-04-27T23:59:59.000Z

371

PROCESS FOR PREPARING URANIUM METAL  

DOE Patents (OSTI)

A process is presented for producing oxygen-free uranium metal comprising contacting iodine vapor with crude uranium in a reaction zone maintained at 400 to 800 C to produce a vaporous mixture of UI/sub 4/ and iodine. Also disposed within the maction zone is a tungsten filament which is heated to about 1600 C. The UI/sub 4/, upon contacting the hot filament, is decomposed to molten uranium substantially free of oxygen.

Prescott, C.H. Jr.; Reynolds, F.L.

1959-01-13T23:59:59.000Z

372

Sources of Radioiodine at Boiling Water Reactors  

Science Conference Proceedings (OSTI)

This report determines specific components in operating BWRs that have a potential for being emission sources of radioactive iodine. Conclusions of this study indicate the following: most radioiodine emanating from plants is from a few major areas; in most cases these releases are locally treatable; the interaction with surfaces is an important phenomenon in the behavior of the iodine; and the chemical form in the plant varies according to the circumstances of release. The models developed provide an imp...

1977-12-01T23:59:59.000Z

373

Fluorine for Hydrogen Exchange in the Hydrofluorobenzene Derivatives C6HxF(6-x), where x = 2, 3, 4 and 5 by Monomeric [1,2,4-(Me3C)3C5H2]2CeH; The Solid State Isomerization of [1,2,4-(Me3C)3C5H2]2Ce(2,3,4,5-C6HF4) to [1,2,4-(Me3C)3C5H2]2Ce(2,3,4,6-C6HF4)  

DOE Green Energy (OSTI)

The reaction between monomeric bis(1,2,4-tri-t-butylcyclopentadienyl)cerium hydride, Cp'2CeH, and several hydrofluorobenzene derivatives is described. The aryl derivatives that are the primary products, Cp'2Ce(C6H5-xFx) where x = 1,2,3,4, are thermally stable enough to be isolated in only two cases, since all of them decompose at different rates to Cp'2CeF and a fluorobenzyne; the latter is trapped by either solvent when C6D6 is used or by a Cp'H ring when C6D12 is the solvent. The trapped products are identified by GCMS analysis after hydrolysis. The aryl derivatives are generated cleanly by reaction of the metallacycle, Cp'((Me3C)2C5H2C(Me2)CH2)Ce, with a hydrofluorobenzene and the resulting arylcerium products, in each case, are identified by their 1H and 19F NMR spectra at 20oC. The stereochemical principle that evolves from these studies is that the thermodynamic isomer is the one in which the CeC bond is flanked by two ortho-CF bonds. This orientation is suggested to arise from the negative charge that is localized on the ipso-carbon atom due to Co(delta+)-Fo(delta-) polarization. The preferred regioisomer is determined by thermodynamic rather than kinetic effects; this is illustrated by the quantitative, irreversible solid-state conversion at 25oC over two months of Cp'2Ce(2,3,4,5-C6HF4) to Cp'2Ce(2,3,4,6-C6HF4), an isomerization that involves a CeC(ipso) for C(ortho)F site exchange.

Andersen, Richard; Werkema, Evan L.; Andersen, Richard A.

2008-04-21T23:59:59.000Z

374

Surface Chemistry and Electrochemistry of Supported Zerovalent Iron Nanoparticles in the Remediation of  

E-Print Network (OSTI)

tanks at the Hanford Site in Washington state, a Department of Energy nuclear weapons production for Creative Work in Fluorine Chemistry. He is a Fellow of the American Association for the Advancement processes in aqueous systems, and new experimental techniques make it possible to probe these frame- works

375

Vanadium-pumped titanium x-ray laser  

DOE Patents (OSTI)

A resonantly photo-pumped x-ray laser (10) is formed of a vanadium (12) and titanium (14) foil combination (16) that is driven by two beams (18, 20) of intense line focused (22, 24) optical laser radiation. Ground state neon-like titanium ions (34) are resonantly photo-pumped by line emission from fluorine-like vanadium ions (32).

Nilsen, Joseph (Livermore, CA)

1992-01-01T23:59:59.000Z

376

Extraction of metals using supercritical fluid and chelate forming legand  

DOE Patents (OSTI)

A method of extracting metalloid and metal species from a solid or liquid material by exposing the material to a supercritical fluid solvent containing a chelating agent is described. The chelating agent forms chelates that are soluble in the supercritical fluid to allow removal of the species from the material. In preferred embodiments, the extraction solvent is supercritical carbon dioxide and the chelating agent is a fluorinated .beta.-diketone. In especially preferred embodiments the extraction solvent is supercritical carbon dioxide, and the chelating agent comprises a fluorinated .beta.-diketone and a trialkyl phosphate, or a fluorinated .beta.-diketone and a trialkylphosphine oxide. Although a trialkyl phosphate can extract lanthanides and actinides from acidic solutions, a binary mixture comprising a fluorinated .beta.-diketone and a trialkyl phosphate or a trialkylphosphine oxide tends to enhance the extraction efficiencies for actinides and lanthanides. The method provides an environmentally benign process for removing contaminants from industrial waste without using acids or biologically harmful solvents. The method is particularly useful for extracting actinides and lanthanides from acidic solutions. The chelate and supercritical fluid can be regenerated, and the contaminant species recovered, to provide an economic, efficient process.

Wai, Chien M. (Moscow, ID); Laintz, Kenneth E. (Los Alamos, NM)

1998-01-01T23:59:59.000Z

377

Fluid extraction  

DOE Patents (OSTI)

A method of extracting metalloid and metal species from a solid or liquid material by exposing the material to a supercritical fluid solvent containing a chelating agent is described. The chelating agent forms chelates that are soluble in the supercritical fluid to allow removal of the species from the material. In preferred embodiments, the extraction solvent is supercritical carbon dioxide and the chelating agent is a fluorinated .beta.-diketone. In especially preferred embodiments the extraction solvent is supercritical carbon dioxide, and the chelating agent comprises a fluorinated .beta.-diketone and a trialkyl phosphate, or a fluorinated .beta.-diketone and a trialkylphosphine oxide. Although a trialkyl phosphate can extract lanthanides and actinides from acidic solutions, a binary mixture comprising a fluorinated .beta.-diketone and a trialkyl phosphate or a trialkylphosphine oxide tends to enhance the extraction efficiencies for actinides and lanthanides. The method provides an environmentally benign process for removing contaminants from industrial waste without using acids or biologically harmful solvents. The method is particularly useful for extracting actinides and lanthanides from acidic solutions. The chelate and supercritical fluid can be regenerated, and the contaminant species recovered, to provide an economic, efficient process.

Wai, Chien M. (Moscow, ID); Laintz, Kenneth E. (Los Alamos, NM)

1999-01-01T23:59:59.000Z

378

Extraction of metals using supercritical fluid and chelate forming ligand  

DOE Patents (OSTI)

A method of extracting metalloid and metal species from a solid or liquid material by exposing the material to a supercritical fluid solvent containing a chelating agent is described. The chelating agent forms chelates that are soluble in the supercritical fluid to allow removal of the species from the material. In preferred embodiments, the extraction solvent is supercritical carbon dioxide and the chelating agent is a fluorinated {beta}-diketone. In especially preferred embodiments the extraction solvent is supercritical carbon dioxide, and the chelating agent comprises a fluorinated {beta}-diketone and a trialkyl phosphate, or a fluorinated {beta}-diketone and a trialkylphosphine oxide. Although a trialkyl phosphate can extract lanthanides and actinides from acidic solutions, a binary mixture comprising a fluorinated {beta}-diketone and a trialkyl phosphate or a trialkylphosphine oxide tends to enhance the extraction efficiencies for actinides and lanthanides. The method provides an environmentally benign process for removing contaminants from industrial waste without using acids or biologically harmful solvents. The method is particularly useful for extracting actinides and lanthanides from acidic solutions. The chelate and supercritical fluid can be regenerated, and the contaminant species recovered, to provide an economic, efficient process. 7 figs.

Wai, C.M.; Laintz, K.E.

1998-03-24T23:59:59.000Z

379

Session II - Programmaster.org  

Science Conference Proceedings (OSTI)

Oct 26, 2009 ... Advances in Energy: Navin Manjooran1; 1Siemens AG ... generation, renewable energy, energy service, power transmission and power distribution. ... All the films were deposited on fluorine doped tin oxide coated glass. ... the impact of germanium (Ge) within an indium-tin-oxide (ITO) conductive matrix.

380

Coordination Chemistry Reviews 256 (2012) 25032520 Contents lists available at SciVerse ScienceDirect  

E-Print Network (OSTI)

orbital; IPCE, incident photon-to-current conversion efficiency; ITO, tin-doped indium oxide; LUMO, lowest, fluorine-doped tin oxide; GC­MS, gas chromatography­mass spectrometry; HOMO, highest occupied molecular.V. 1. Introduction The quest for abundant, renewable energy is currently one of society's greatest

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


381

Introduction As discussed in other articles in this issue,  

E-Print Network (OSTI)

(Figure 3a).4,10 Fluorine- doped tin oxide is preferred for the trans- parent electrode over indium tin oxide because indium diffuses into the titania when it is heated to 400 C. We have found that open Renewable Energy Laboratory.) #12;adjusting the time used for the melt infil- tration.9 A 30-nm

McGehee, Michael

382

ISSN:1369 7021 Elsevier Ltd 2007NOVEMBER 2007 | VOLUME 10 | NUMBER 1128 Polymer-based solar  

E-Print Network (OSTI)

. 2b) sandwiched between a transparent conductor such as indium-tin-oxide (ITO) coated with poly(3,4-ethylenedioxythiophene): poly(styrene sulfanate) (PEDOT:PSS) or fluorinated tin oxide (FTO), and a reflecting metal by the National Renewable Energy Laboratory (NREL), but some have been corroborated by several groups. The key

McGehee, Michael

383

Please cite this article in press as: K.J. Young, et al., Coord. Chem. Rev. (2012), http://dx.doi.org/10.1016/j.ccr.2012.03.031 ARTICLE IN PRESS  

E-Print Network (OSTI)

orbital; IPCE, incident photon-to-current conversion efficiency; ITO, tin-doped indium oxide; LUMO, lowest, fluorine-doped tin oxide; GC­MS, gas chromatography­mass spectrometry; HOMO, highest occupied molecular for abundant, renewable energy is currently one of society's greatest technological challenges. Light energy

384

PROCESS FOR CONTINUOUSLY SEPARATING IRRADIATION PRODUCTS OF THORIUM  

DOE Patents (OSTI)

A method is presented for separating uranium-233 and protactinium from thorium-232 containing compositions which comprises irradiating finely divided particles of said thorium with a neutron flux to form uranium-233 and protactinium, heating the neutron-irradiated composition in a fluorine and hydrogen atmosphere to form volatile fluorides of uranium and protactinium and thereafter separating said volatile fluorides from the thorium.

Hatch, L.P.; Miles, F.T.; Sheehan, T.V.; Wiswall, R.H.; Heus, R.J.

1959-07-01T23:59:59.000Z

385

Method for converting asbestos to non-carcinogenic compounds  

DOE Patents (OSTI)

Hazardous and carcinogenic asbestos waste characterized by a crystalline fibrous structure is transformed into non-carcinogenic, relatively nonhazardous, and non-crystalline solid compounds and gaseous compounds which have commercial utilization. The asbestos waste is so transformed by the complete fluorination of the crystalline fibrous silicate mineral defining the asbestos. 7 figs.

Selby, T.W.

1996-08-06T23:59:59.000Z

386

The toxicity of X material  

SciTech Connect

This report addresses toxicity (largely chemical) of Manhattan Project materials from the point of worker protection. Known chemical toxicities of X material (uranium), nitrous fumes, fluorine, vanadium, magnesium, and lime are described followed by safe exposure levels, symptoms of exposure, and treatment recommendations. The report closes with an overview of general policy in a question and answer format.

Ferry, J.L.

1943-12-31T23:59:59.000Z

387

Summary of research of the section on pharmacology. Progress report for December 1944  

SciTech Connect

Various studies relating the biological and behavioral effect of several uranium fluorides and chlorides as well as fluorine and oxyflourides are related. Most of these studies involved rats, guinea pigs, rabbits or dogs. Route of administration included inhalation, ingestion, or application to the skin.

Hodge, H.C.

1944-12-31T23:59:59.000Z

388

22nd European Photovoltaic Solar Energy Conference, Fiera Milano, Italy, 3-7 September 2007 Version: 30 August 2007  

E-Print Network (OSTI)

(F-gases) which are used, or considered to be used, in crystalline silicon photovoltaic solar cell22nd European Photovoltaic Solar Energy Conference, Fiera Milano, Italy, 3-7 September 2007 Version: 30 August 2007 FLUORINATED GREENHOUSE GASES IN PHOTOVOLTAIC MODULE MANUFACTURING: POTENTIAL EMISSIONS

389

Criticality safety considerations for MSRE fuel drain tank uranium aggregation  

SciTech Connect

This paper presents the results of a preliminary criticality safety study of some potential effects of uranium reduction and aggregation in the Molten Salt Reactor Experiment (MSRE) fuel drain tanks (FDTs) during salt removal operations. Since the salt was transferred to the FDTs in 1969, radiological and chemical reactions have been converting the uranium and fluorine in the salt to UF{sub 6} and free fluorine. Significant amounts of uranium (at least 3 kg) and fluorine have migrated out of the FDTs and into the off-gas system (OGS) and the auxiliary charcoal bed (ACB). The loss of uranium and fluorine from the salt changes the chemical properties of the salt sufficiently to possibly allow the reduction of the UF{sub 4} in the salt to uranium metal as the salt is remelted prior to removal. It has been postulated that up to 9 kg of the maximum 19.4 kg of uranium in one FDT could be reduced to metal and concentrated. This study shows that criticality becomes a concern when more than 5 kg of uranium concentrates to over 8 wt% of the salt in a favorable geometry.

Hollenbach, D.F.; Hopper, C.M. [Oak Ridge National Lab., TN (United States). Computational Physics and Engineering Div.

1997-03-01T23:59:59.000Z

390

RADIATION EFFECTS OF ALPHA PARTICLES ON URANIUM HEXAFLUORIDE  

SciTech Connect

Alpha irradiation of uranium hexafluoride results in the formation of fluorine and intermediate, solid uranium fluorides: these products react with each other, apparently by a radiation-induced process. to reform uranium hexifluoride. The number of molecules of uranium hexafluoride decomposed, excluding recombiapproximately 1 in the temperature range 21 to 87 deg C. Irradiation of a mixture of fluorine and uranium hexafluoride in a vessel containing uranium fluorides substantistes the postulated mechanism. At fluorine pressures of 50 to 100 mm Hg, there is an increase, rather than a decrease, in uranium hexafluoride pressure. Rates of both decomposition and recombination processes appear to depend only on the rates of radiation energy absorption. Equations formnulated to describe the combined decomposition and reformation reactions can be used to calculate equilibrium concentrations of uranium hexfluoride and fluorine when the intensity of the radiation source is defined. The effects of three diluent gases, helium, nitrogen and oxygen, were studied in an attempt to find possible electron transfer processes. (auth)

Bernhardt, H.A.; Davis, W. Jr.; Shiflett, C.H.

1958-06-01T23:59:59.000Z

391

RECOVERY OF METAL VALUES FROM AQUEOUS SOLUTIONS BY SOLVENT EXTRACTION  

DOE Patents (OSTI)

An organic solvent mixure is described for extracting actinides from aqueous solutions; the solvent mixture consists of from 10 to 25% by volume of tributyl phosphate and the remainder a chlorine-fluorine-substituted saturated hydrocarbon having two carbon atoms in the molecule.

Moore, R.L.

1959-09-01T23:59:59.000Z

392

The use of high glass temperature polymers in the production of transparent, structured surfaces using nanoimprint lithography  

Science Conference Proceedings (OSTI)

Polymers with high glass transition temperatures, fluorinated ethylene propylene copolymer (FEP) and poly(ethylene naphthalate) (PEN), have been used in imprint lithography as a protective support layer and as a secondary mould, to imprint superficial ... Keywords: Embossing, Nanoimprint lithography, Polymer Engineering

Christopher A. Mills; Javier G. Fernandez; Abdelhamid Errachid; Josep Samitier

2008-09-01T23:59:59.000Z

393

Vanadium-pumped titanium x-ray laser  

DOE Patents (OSTI)

A resonantly photo-pumped x-ray laser is formed of a vanadium and titanium foil combination that is driven by two beams of intense line focused optical laser radiation. Ground state neon-like titanium ions are resonantly photo-pumped by line emission from fluorine-like vanadium ions.

Nilsen, J.

1991-02-13T23:59:59.000Z

394

Refractive index and density in F- and Cl-doped silica glasses  

Science Conference Proceedings (OSTI)

The refractive index and density of fluorine- and chlorine-doped silica glasses were measured as functions of fictive temperature. The halogen concentrations were observed to have a refractive index or density that is independent of the fictive temperature were found. This implies that these properties are not affected by any heat-treatment conditions.

Kakiuchida, Hiroshi; Shimodaira, Noriaki; Sekiya, Edson H.; Saito, Kazuya; Ikushima, Akira J. [Research Center for Advanced Photon Technology, Toyota Technological Institute, 2-12-1 Hisakata, Tempaku, Nagoya, Aichi 468-8511 (Japan); Research Center for Advanced Photon Technology, Toyota Technological Institute, 2-12-1 Hisakata, Tempaku, Nagoya, Aichi 468-8511, Japan and Research Center, Asahi Glass Co., Ltd., 1150 Hazawa-cho, Kanagawa, Yokohama, Kanagawa 221-8755 (Japan); Research Center for Advanced Photon Technology, Toyota Technological Institute, 2-12-1 Hisakata, Tempaku, Nagoya, Aichi 468-8511 (Japan)

2005-04-18T23:59:59.000Z

395

PROCESS FOR PRODUCING URANIUM HEXAFLUORIDE  

DOE Patents (OSTI)

A process for the production of uranium hexafluoride from the oxides of uranium is reported. In accordance with the method the higher oxides of uranium may be reduced to uranium dioxide (UO/sub 2/), the latter converted into uranium tetrafluoride by reaction with hydrogen fluoride, and the UF/sub 4/ convented to UF/sub 6/ by reaction with a fluorinating agent. The UO/sub 3/ or U/sub 3/O/sub 8/ is placed in a reaction chamber in a copper boat or tray enclosed in a copper oven, and heated to 500 to 650 deg C while hydrogen gas is passed through the oven. The oven is then swept clean of hydrogen and the water vapor formed by means of nitrogen and then while continuing to maintain the temperature between 400 and 600 deg C, anhydrous hydrogen fluoride is passed through. After completion of the conversion to uranium tetrafluoride, the temperature of the reaction chamber is lowered to ahout 400 deg C, and elemental fluorine is used as the fluorinating agent for the conversion of UF/sub 4/ into UF/sub 6/. The fluorine gas is passed into the chamber, and the UF/sub 6/ formed passes out and is delivered to a condenser.

Fowler, R.D.

1957-10-22T23:59:59.000Z

396

Method of bonding diamonds in a matrix and articles thus produced  

DOE Patents (OSTI)

By fluorinating diamond grit, the grit may be readily bonded into a fluorocarbon resin matrix. The matrix is formed by simple hot pressing techniques. Diamond grinding wheels may advantageously be manufactured using such a matrix. Teflon fluorocarbon resins are particularly well suited for using in forming the matrix.

Taylor, G.W.

1981-01-27T23:59:59.000Z

397

Fuel cell electrolyte membrane with basic polymer  

DOE Patents (OSTI)

The present invention is an electrolyte membrane comprising an acid and a basic polymer, where the acid is a low-volatile acid that is fluorinated and is either oligomeric or non-polymeric, and where the basic polymer is protonated by the acid and is stable to hydrolysis.

Larson, James M. (Saint Paul, MN); Pham, Phat T. (Little Canada, MN); Frey, Matthew H. (Cottage Grove, MN); Hamrock, Steven J. (Stillwater, MN); Haugen, Gregory M. (Edina, MN); Lamanna, William M. (Stillwater, MN)

2010-11-23T23:59:59.000Z

398

Identification and characterization of conservative organic tracers for use as hydrologic tracers for the Yucca Mountain Site characterization study; Progress report, April 1, 1993--June 30, 1993  

Science Conference Proceedings (OSTI)

This report is in two parts one for the fluorinated benzoic acids and one for the fluorinated aliphatic acids. The assumptions made in the report regarding the amount of tracer that will be used, dilution of the tracer during the test and the length of exposure (if any) to individuals drinking the water were made by the authors. These assumptions must really come from the USGS hydrologists in charge of the c-well tracer testing program. Accurate estimates of dilution of the tracer during the test are also important because of solubility limitations of some of the tracers. Three of the difluorobenzoic acids have relatively low solubilities and may not be usable if the dilution estimates are large. The toxicologist that reviewed the document agreed with our conclusion that the fluorinated benzoic and toluic acids do not represent a health hazard if used under the conditions as outlined in the report. We are currently testing 15 of these compounds, and if even if three difluorobenzoic acids cannot be used because of solubility limitations we will still have 12 tracers. The toxicologist felt that the aliphatic fluorinated acids potentially present more of a health risk than the aromatic. This assessment was based on the fact of a known allergic response to halothane anesthetic. This risk, although minimal, is known and he felt that was enough reason to recommend against their use. The authors feel that the toxicologists interpretation of this risk was overly conservative, however, we will not go against his recommendation at this time for the following reasons. First, without the aliphatic compounds we still have 12 to 15 fluorinated aromatic acids which, should be enough for the c-well tests. Second, to get a permit to use aliphatic compounds would undoubtedly require a hearing which could be quite lengthy.

Dombrowski, T.; Stetzenbach, K.

1993-08-01T23:59:59.000Z

399

A Study of the Stability and Characterization Plutonium Dioxide and Chemical Characterization [of] Rocky Flats and Los Alamos Plutonium-Containing Incinerator Ash  

SciTech Connect

In the presentation ''A Study of the Stability and Characterization of Plutonium Dioxide'', the authors discuss their recent work on actinide stabilities and characterization, in particular, plutonium dioxide PuO{sub 2}. Earlier studies have indicated that PuO{sub 2} has the fluorite structure of CaF{sub 2} and typical oxide semiconductor properties. However, detailed results on the bulk electronic structure of this important actinide oxide have not been available. The authors have used all-electron, full potential linear combinations Gaussian type orbitals fitting function (LCGTO-FF) method to study PuO{sub 2}. The LCGTO-FF technique characterized by its use of three independent GTO basis sets to expand the orbitals, charge density, and exchange-correlation integral kernels. Results will be presented on zero pressure using both the Hedin-Lundquist local density approximation (LDA) model or the Perdew-Wang generalized gradient approximation (GGA) model. Possibilities of different characterizations of PuO{sub 2} will be explored. The paper ''Chemical Characterization Rocky Flats and Los Alamos Plutonium-Containing Incinerator Ash'' describes the results of a comprehensive study of the chemical characteristics of virgin, calcined and fluorinated incinerator ash produced at the Rocky Flats Plant and at the Los Alamos National Laboratory prior to 1988. The Rocky Flats and Los Alamos virgin, calcined, and fluorinated ashes were also dissolved using standard nitrate dissolution chemistry. Corresponding chemical evaluations were preformed on the resultant ash heel and the results compared with those of the virgin ash. Fluorination studies using FT spectroscopy as a diagnostic tool were also performed to evaluate the chemistry of phosphorus, sulfur, carbon, and silicon containing species in the ash. The distribution of plutonium and other chemical elements with the virgin ash, ash heel, fluorinated ash, and fluorinated ash heel particulates were studied in detail using microprobe analysis. Some of the more interesting results of these investigations are presented.

Ray, A.K.; Boettger, J.C.; Behrens, Robert G.

1999-11-29T23:59:59.000Z

400

Test results from the GA technologies engineering-scale off-gas treatment system  

SciTech Connect

One method for reducing the volume of HTGR fuel prior to reprocessing or spent fuel storage is to crush and burn the graphite fuel elements. The burner off-gas (BOG) contains radioactive components, principally H-3, C-14, Kr-85, I-129, and Rn-220, as well as chemical forms such as CO/sub 2/, CO, O/sub 2/, and SO/sub 2/. The BOG system employs components designed to remove these constitutents. Test results are reported for the iodine and SO/sub 2/ adsorbers and the CO/HT oxidizer. Silver-based iodine adsorbents were found to catalyze the premature conversion of CO to CO/sub 2/. Subsequent tests showed that iodine removal could not be performed downstream of the CO/HT oxidizer since iodine in the BOG system rapidly deactivated the Pt-coated alumina CO catalyst. Lead-exchanged zeolite (PbX) was found to be an acceptable alternative for removing iodine from BOG without CO conversion. Intermittent and steady-state tests of the pilot-plant SO/sub 2/ removal unit containing sodium-exchanged zeolite (NaX) demonstrated that decontamination factors greater than or equal to 100 could be maintained for up to 50 h. In a reprocessing flowsheet, the solid product from the burners is dissolved in nitric or Thorex acid. The dissolver off-gas (DOG) contains radioactive components H-3, Kr-85, I-129, Rn-220 plus chemical forms such as nitrogen oxides (NO/sub x/). In the pilot-scale system at GA, iodine is removed from the DOG by adsorption. Tests of iodine removal have been conducted using either silver-exchanged mordenite (AgZ) or AgNO/sub 3/-impregnated silica gel (AC-6120). Although each sorbent performed well in the presence of NO/sub x/, the silica gel adsorbent proved more efficient in silver utilization and, thus, more cost effective.

Jensen, D.D.; Olguin, L.J.; Wilbourn, R.G.

1984-06-01T23:59:59.000Z

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


401

Evaluation of the contamination of marine algae (seaweed) from the St. Lawrence River and likely to be consumed by humans  

SciTech Connect

The goal of the study was to assess the contamination of marine algae (seaweeds) growing in the St. Lawrence River estuary and Gulf of St. Lawrence and to evaluate the risks to human health from the consumption of these algae. Algae were collected by hand at low tide. A total of 10 sites on the north and south shores of the St. Lawrence as well as in Baie des Chaleurs were sampled. The most frequently collected species of algae were Fucus vesiculosus, Ascophyllum nodosum, Laminaria Longicruris, Palmaria palmata, Ulva lactuca, and Fucus distichus. Alga samples were analyzed for metals iodine, and organochlorines. A risk assessment was performed using risk factors. In general, concentrations in St. Lawrence algae were not very high. Consequently, health risks associated with these compounds in St. Lawrence algae were very low. Iodine concentration, on the other hand, could be of concern with regard to human health. Regular consumption of algae, especially of Laminaria sp., could result in levels of iodine sufficient to cause thyroid problems. For regular consumers, it would be preferable to choose species with low iodine concentrations, such as U. lactuca and P. palmata, in order to prevent potential problems. Furthermore, it would also be important to assess whether preparation for consumption or cooking affects the iodine content of algae. Algae consumption may also have beneficial health effects. Scientific literature has shown that it is a good source of fiber and vitamins, especially vitamin B{sub 12}.

Phaneuf, D.; Cote, I.; Dumas, P.; Ferron, L.A.; LeBlanc, A. [CHUQ, Sainte-Foy, Quebec (Canada). Centre de Toxicologie du Quebec

1999-02-01T23:59:59.000Z

402

NA Standards | Refinement Parameters | X-PLOR param file for high  

NLE Websites -- All DOE Office Websites (Extended Search)

the file for different bond distances and angles of C2'and C3'-endo the file for different bond distances and angles of C2'and C3'-endo remark K= scale*(kT/sigma**2), scales=Base 0.1875, Sugar 0.566, Phos 1.548 ! removed references to CA, CF, CS, MG, NH3, OS (ATB 12/30/94) ! removed TIP3 water model (ATB 12/30/94) ! mapped NA->NNA, CH3E->CC3E (ATB 12/30/94) ! G.PARKINSON, J.VOJTECHOVSKY, L.CLOWNEY, A.T.BRUNGER ! H.M.BERMAN ! NEW PARAMETERS FOR THE REFINEMENT OF NUCLEIC ACID CONTAINING ! STRUCTURES ! ACTA CRYST.D (1996) v. 52 57-64 set echo=false end !the generic bonds were taken from param11.dna with 3*kq bond C5R OH 876.000 1.4300 ! 5' end bond C5D OH 876.000 1.4300 ! 5' end bond C3R OH 876.000 1.4300 ! 3' end bond C3D OH 876.000 1.4300 ! 3' end bond HHO O2R 1350.000 0.9572 !Mod HO to HHO 05/15/96

403

Photovoltaics and the Environment  

DOE Green Energy (OSTI)

Over the past five years, solar energy usage has grown by about 43 percent a year, giving rise to a billion-dollar industry in photovoltaics (PV) or getting electricity from light. The word photovoltaics combines the Greek phos, or light, with the “volt” of electricity. PV technologies have distinct environmental advantages over conventional power technologies, such as: no noise, no emissions, no need for fuel and power lines. Compared to burning coal, a gigawatt-hour of PV-generated electricity would prevent the release of about 1,000 tons of carbon dioxide, eight of sulfur dioxide, four of nitrogen oxides, and 0.4 tons of particulates. However, manufacturing the solar cells that transform light to electricity requires the use of some toxic and flammable substances. Addressing the environmental, health, and safety concerns of the PV industry to minimize risk while ensuring economic viability and public support is the work of the National Photovoltaic Environmental Health, & Safety Assistance Center at BNL.

Fthenakis, Vasilis (BNL Environmental Sciences)

2005-09-21T23:59:59.000Z

404

The synthesis, characterization and reactivity of high oxidation state nickel fluorides  

Science Conference Proceedings (OSTI)

The research described in this thesis has mainly addressed the challenge of the synthesis of thermodynamically unstable nickel fluorides, which cannot be made by traditional thermal methods. A low-temperature approach towards the synthesis of such transition metal fluorides exploits the greater thermodynamic stability of high oxidation states in anions and involves the use of anhydrous hydrogen fluoride (aHF) as a solvent. The general method consists of combining an aHF soluble starting material (e.g., K{sub 2}NiF{sub 6}) with a Lewis fluoroacid (e.g., BF{sub 3}), which precipitates a neutral polymeric solid state fluoride: 2 K{sup +} + NiF{sub 6}{sup 2{minus}} + BF{sub 3} {r_arrow} NiF{sub 4} + 2 BF{sub 4}{sup {minus}} + 2 K{sup +}. At room temperature, this reaction yields a different structural phase, with composition K{sub x}NiF{sub 3} (x {approx} 0.18). This material has a pseudo-hexagonal tungsten bronze structure (H{sub 0}-K{sub x}NiF{sub 3}), and is an ionic conductor, probably due to K{sup +} ions hosted in the lattice channels. R-NiF{sub 3} is capable of fluorinating a wide range of inorganic and organic substrates. These reactions have probably shed light on the mechanism of the Simons Electrochemical Fluorination (ECF) Process, an important industrial method of fluorinating organic compounds. It has long been speculated that NiF{sub 3} plays a role in the ECF process, which uses nickel electrodes in aHF solvent. K{sub 2}NiF{sub 6} also fluorinates organic compounds in aHF, but interestingly, yields different fluorinated products. The reduction of R-NiF{sub 3} and K{sub 2}NiF{sub 6} during fluorination reactions yields NiF{sub 2}. A method has been developed to regenerate NiF{sub 6}{sup 2{minus}} from NiF{sub 2}.

Chacon, L.C. [Univ. of Berkeley, CA (United States). Dept. of Chemistry]|[Lawrence Berkeley National Lab., CA (United States). Chemical Sciences Div.

1997-12-01T23:59:59.000Z

405

Structure-property relationship of metal-organic frameworks (MOFs) and physisorbed off-gas radionuclides.  

Science Conference Proceedings (OSTI)

We report on the host-guest interactions between metal-organic frameworks (MOFs) with various profiles and highly polarizable molecules (iodine), with emphasis on identifying preferential sorption sites in these systems. Radioactive iodine 129I, along with other volatile radionuclides (3H, 14C, Xe and Kr), represents a relevant component in the off-gas resulted during nuclear fuel reprocessing. Due to its very long half-life, 15.7 x 106 years, and potential health risks in humans, its efficient capture and long-term storage is of great importance. The leading iodine capture technology to date is based on trapping iodine in silver-exchanged mordenite. Our interests are directed towards improving existent capturing technologies, along with developing novel materials and alternative waste forms. Herein we report the first study that systematically monitors iodine loading onto MOFs, an emerging new class of porous solid-state materials. In this context, MOFs are of particular interest as: (i) they serve as ideal high capacity storage media, (ii) they hold potential for the selective adsorption from complex streams, due to their high versatility and tunability. This work highlights studies on both newly developed in our lab, and known highly porous MOFs that all possess distinct characteristics (specific surface area, pore volume, pore size, and dimension of the window access to the pore). The materials were loaded to saturation, where elemental iodine was introduced from solution, as well as from vapor phase. Uptakes in the range of {approx}125-150 wt% I2 sorbed were achieved, indicating that these materials outperform all other solid adsorbents to date in terms of overall capacity. Additionally, the loaded materials can be efficiently encapsulated in stable waste forms, including as low temperature sintering glasses. Ongoing studies are focused on gathering qualitative information with respect to localizing the physisorbed iodine molecules within the frameworks: X-ray single-crystal analyses, in conjunction with high pressure differential pair distribution function (d-PDF) studies aimed to identify preferential sites in the pores, and improve MOFs robustness. Furthermore, durability studies on the iodine loaded MOFs and subsequent waste forms include thermal analyses, SEM/EDS elemental mapping, and leach-durability testing. We anticipate for this in-depth analysis to further aid the design of advanced materials, capable to address major hallmarks: safe capture, stability and durability over extended timeframes.

Nenoff, Tina Maria; Chupas, Peter J. (Argonne National Laboratory); Garino, Terry J.; Rodriguez, Mark Andrew; Chapman, Karena W. (Argonne National Laboratory); Sava, Dorina Florentina

2010-11-01T23:59:59.000Z

406

Site specific incorporation of heavy atom-containing unnatural amino acids into proteins for structure determination  

DOE Patents (OSTI)

Translation systems and other compositions including orthogonal aminoacyl tRNA-synthetases that preferentially charge an orthogonal tRNA with an iodinated or brominated amino acid are provided. Nucleic acids encoding such synthetases are also described, as are methods and kits for producing proteins including heavy atom-containing amino acids, e.g., brominated or iodinated amino acids. Methods of determining the structure of a protein, e.g., a protein into which a heavy atom has been site-specifically incorporated through use of an orthogonal tRNA/aminoacyl tRNA-synthetase pair, are also described.

Xie, Jianming (San Diego, CA); Wang, Lei (San Diego, CA); Wu, Ning (Boston, MA); Schultz, Peter G. (La Jolla, CA)

2008-07-15T23:59:59.000Z

407

Improved method for preparing rare earth sesquichalcogenides  

DOE Patents (OSTI)

An improved method for the preparation of high purity rare earth sesquichalcogenides is described. The rare earth, as one or more pieces of the metal, is sealed under a vacuum with a stoichiometric amount of sulfur or selenium and a small amount of iodine into a quartz reaction vessel. The sealed vessel is then heated to above the vaporization temperature of the chalcogen and below the melting temperature of the rare earth metal and maintained until the product has been formed. The iodine is then vaporized off leaving a pure product. The rare earth sulfides and selenides thus formed are useful as semiconductors and as thermoelectric generators. 3 tables.

Takeshita, T.; Beaudry, B.J.; Gschneidner, K.A. Jr.

1982-04-14T23:59:59.000Z

408

It's Elemental - Isotopes of the Element Oxygen  

NLE Websites -- All DOE Office Websites (Extended Search)

Nitrogen Nitrogen Previous Element (Nitrogen) The Periodic Table of Elements Next Element (Fluorine) Fluorine Isotopes of the Element Oxygen [Click for Main Data] Most of the isotope data on this site has been obtained from the National Nuclear Data Center. Please visit their site for more information. Naturally Occurring Isotopes Mass Number Natural Abundance Half-life 16 99.757% STABLE 17 0.038% STABLE 18 0.205% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 12 1.139×10-21 seconds Proton Emission No Data Available 13 8.58 milliseconds Electron Capture 100.00% Electron Capture with delayed Proton Emission 100.00% 14 70.620 seconds Electron Capture 100.00% 15 122.24 seconds Electron Capture 100.00% 16 STABLE - - 17 STABLE - - 18 STABLE - - 19 26.88 seconds Beta-minus Decay 100.00%

409

It's Elemental - The Element Oxygen  

NLE Websites -- All DOE Office Websites (Extended Search)

Nitrogen Nitrogen Previous Element (Nitrogen) The Periodic Table of Elements Next Element (Fluorine) Fluorine The Element Oxygen [Click for Isotope Data] 8 O Oxygen 15.9994 Atomic Number: 8 Atomic Weight: 15.9994 Melting Point: 54.36 K (-218.79°C or -361.82°F) Boiling Point: 90.20 K (-182.95°C or -297.31°F) Density: 0.001429 grams per cubic centimeter Phase at Room Temperature: Gas Element Classification: Non-metal Period Number: 2 Group Number: 16 Group Name: Chalcogen What's in a name? From the greek words oxys and genes, which together mean "acid forming." Say what? Oxygen is pronounced as OK-si-jen. History and Uses: Oxygen had been produced by several chemists prior to its discovery in 1774, but they failed to recognize it as a distinct element. Joseph

410

Network flow model analysis of the impact of chlorofluorocarbon phaseout on acid-grade fluorspar. Information circular/1994  

SciTech Connect

Chlorofluorocarbons (CFC`s) are being phased out and eventually banned under extensive international agreements because the chlorine in CFC`s is thought to deplete the Earth`s ozone layer. As a result, the fluorspar mining industry, which is the source of fluorine in fluorocarbons through intermediate hydrofluoric acid, is being affected. Concern for this impact has led the U.S. Bureau of Mines to employ its capabilities to analyze various scenarios in the evolution of CFC replacements and substitutes to determine their effect on fluorspar mining. This report utilizes a network flow model to examine the effects of proposed replacements for CFC`s, in terms of fluorine content, on fluorspar operations worldwide and on hydrofluoric acid plants in North America and Europe.

Slatnick, J.A.; Fulton, R.B.

1994-12-31T23:59:59.000Z

411

Long-range global warming impact of gaseous diffusion plant operation  

SciTech Connect

The DOE gaseous diffusion plant complex makes extensive use of CFC-114 as a primary coolant. As this material is on the Montreal Protocol list of materials scheduled for production curtailment, a substitute must be found. In addition to physical cooling properties, the gaseous diffusion application imposes the unique requirement of chemical inertness to fluorinating agents. This has narrowed the selection of a near-term substitute to two fully fluorinated material, FC-318 and FC-3110, which are likely to be strong, long-lived greenhouse gases. In this document, calculations are presented showing, for a number of plausible scenarios of diffusion plant operation and coolant replacement strategy, the future course of coolant use, greenhouse gas emissions (including coolant and power-related indirect CO{sub 2} emissions), and the consequent global temperature impacts of these scenarios.

Trowbridge, L.D.

1992-09-01T23:59:59.000Z

412

Electrochemical method of producing eutectic uranium alloy and apparatus  

DOE Patents (OSTI)

An apparatus and method for continuous production of liquid uranium alloys through the electrolytic reduction of uranium chlorides. The apparatus includes an electrochemical cell formed from an anode shaped to form an electrolyte reservoir, a cathode comprising a metal, such as iron, capable of forming a eutectic uranium alloy having a melting point less than the melting point of pure uranium, and molten electrolyte in the reservoir comprising a chlorine or fluorine containing salt and uranium chloride. The method of the invention produces an eutectic uranium alloy by creating an electrolyte reservoir defined by a container comprising an anode, placing an electrolyte in the reservoir, the electrolyte comprising a chlorine or fluorine containing salt and uranium chloride in molten form, positioning a cathode in the reservoir where the cathode comprises a metal capable of forming an uranium alloy having a melting point less than the melting point of pure uranium, and applying a current between the cathode and the anode.

Horton, James A. (Livermore, CA); Hayden, H. Wayne (Oakridge, TN)

1995-01-01T23:59:59.000Z

413

Optimization of transparent and reflecting electrodes for amorphous-silicon solar cells. Final subcontract report, 1 May 1991--30 April 1994  

DOE Green Energy (OSTI)

Fluorine-doped zinc oxide was shown to have the lowest absorption loss of any of the known transparent conductors. An apparatus was constructed to deposit textured, transparent, conductive, fluorine-doped zinc oxide layers with uniform thickness over a 10 cm by 10 cm area, using inexpensive, high-productivity atmospheric pressure chemical vapor deposition. Amorphous silicon solar cells grown on these textured films show very high peak quantum efficiencies (over 90%). However, a significant contact resistance develops at the interface between the amorphous silicon and the zinc oxide. Transparent, conductive gallium-doped zinc oxide films were grown by APCVD at a low enough temperature (260{degree}C) to be deposited on amorphous silicon as a final conductive back contact to solar cells. A quantum-mechanical theory of bonding was developed and applied to some metal oxides; it forms a basis for understanding TCO structures and the stability of their interfaces with silicon.

Gordon, R.G.; Hu, J.; Lacks, D.; Musher, J.; Thornton, J.; Liang, H. [Harvard Univ., Cambridge, MA (United States)

1994-07-01T23:59:59.000Z

414

Method for processing aluminum spent potliner in a graphite electrode ARC furnace  

SciTech Connect

A method of processing spent aluminum pot liner containing carbon, cyanide compositions, fluorides and inorganic oxides. The spent aluminum pot liner is crushed iron oxide is added to form an agglomerated material. The agglomerated material is melted in an electric arc furnace having the electrodes submerged in the molten material to provide a reducing environment during the furnace operation. In the reducing environment, pot liner is oxidized while the iron oxides are reduced to produce iron and a slag substantially free of cyanide compositions and fluorides. An off-gas including carbon oxides and fluorine is treated in an air pollution control system with an afterburner and a scrubber to produce NaF, water and a gas vented to the atmosphere free of cyanide compositions, fluorine and CO.

O' Connor, William K. (Lebanon, OR); Turner, Paul C. (Independence, OR); Addison, Gerald W. (St. Stephen, SC)

2002-12-24T23:59:59.000Z

415

Sources of carrier F-19 in F-18 fluoride  

SciTech Connect

Fluorine-18 is used for many PET radiopharmaceuticals. Theoretically {sup 18}F should be carrier free and a good candidate for nanochemistry. However, {sup 18}F has 10 to 1000 times more stable fluorine atoms than radioactive atoms. In order to understand the source of carrier fluoride and other ions associated with {sup 18}F radiosynthesis, anion concentrations of different components of {sup 18}F target systems as well as solvents and chemicals used in radiosynthesis were measured. Results: The enriched water used for production of {sup 18}F had low levels of anions. In general, the sources of anions, particularly of fluoride, were the chemical reagents used for synthesis and trace contaminants in tubing, valves and fittings. A major component of contamination was nitrate from irradiation of dissolved nitrogen gas in the target water.

Link, J. M.; Shoner, S. C.; Krohn, K. A. [University of Washington, Department of Radiology, Molecular Imaging Center, 1959 NE Pacific St., Box 356004, Seattle, WA 98195-6004 (United States)

2012-12-19T23:59:59.000Z

416

LOW-TEMPERATURE REFLUORINATION OF PuF$sub 6$ DECOMPOSITION PRODUCTS  

SciTech Connect

The use of direct refluorinntion to recover plutonium deposited in equipment by consumption and decomposition of PuF/sub 6/ gas was the subject of a brief experimental program Measurable rates of refluorination were obtained at temperatures as low as 170 C and by means of a statistically dcsigned experiment; the approximate signficance of the three variables, temperature, fluorine pressure, and fluorine flow rate, was determined. Temperature was found to be the most significant variable, and the heat of reaction based on removal rates measured from 170 to 350 C compared favorably with reported values obtained by equilibrating PuF/sub 6/ and F2 gas mixtures. At plutonium surface concentrntions below -3 mu g/cm, the rate of refluorination was found to be proportional to the plutonium surface concentration. In no case was the surface concentration decreased below 0.08 mu g/cm2. (auth)

Robb, W.L.; Brandon, R.J.; Myers, R.L.; Galpern, H.N.

1957-03-30T23:59:59.000Z

417

Study of heavy ion induced fission fragment angular and mass distribution at near and sub-coulomb barrier energies  

E-Print Network (OSTI)

The thesis presents investigations on the angular and mass distribution of fission fragments on heavy ion induced fission reactions. The present investigations address current issues in heavy ion induced fission reactions like finding the optimum entrance channel for the synthesis of super heavy elements (SHE). A double arm time of flight spectrometer over long flight path was used to measure the precise masses of complementary fission fragments. Necessary large area position sensitive gas detectors, the method of experiments and data analysis were developed. The first string of measurements were for a spherical target (209^Bi) with oxygen and fluorine projectiles. The next series of experiments were done using a deformed target (232^Th) with fluorine, oxygen and carbon projectiles.

T. K. Ghosh

2005-08-10T23:59:59.000Z

418

Apparatus and method for atmospheric pressure reactive atom plasma processing for shaping of damage free surfaces  

DOE Patents (OSTI)

Fabrication apparatus and methods are disclosed for shaping and finishing difficult materials with no subsurface damage. The apparatus and methods use an atmospheric pressure mixed gas plasma discharge as a sub-aperture polisher of, for example, fused silica and single crystal silicon, silicon carbide and other materials. In one example, workpiece material is removed at the atomic level through reaction with fluorine atoms. In this example, these reactive species are produced by a noble gas plasma from trace constituent fluorocarbons or other fluorine containing gases added to the host argon matrix. The products of the reaction are gas phase compounds that flow from the surface of the workpiece, exposing fresh material to the etchant without condensation and redeposition on the newly created surface. The discharge provides a stable and predictable distribution of reactive species permitting the generation of a predetermined surface by translating the plasma across the workpiece along a calculated path.

Carr; Jeffrey W. (Livermore, CA)

2009-03-31T23:59:59.000Z

419

Method for processing aluminum spent potliner in a graphite electrode arc furnace  

DOE Patents (OSTI)

A method of processing spent aluminum pot liner containing carbon, cyanide compositions, fluorides and inorganic oxides. The spend aluminum pot liner is crushed, iron oxide is added to form an agglomerated material. The agglomerated material is melted in an electric arc furnace having the electrodes submerged in the molten material to provide a reducing environment during the furnace operation. In the reducing environment, pot liner is oxidized while the iron oxides are reduced to produce iron and a slag substantially free of cyanide compositions and fluorides. An off-gas including carbon oxides and fluorine is treated in an air pollution control system with an afterburner and a scrubber to produce NaF, water and a gas vented to the atmosphere free of cyanide compositions, fluorine, and CO.

O' Connor, William K.; Turner, Paul C.; Addison, G.W. (AJT Enterprises, Inc.)

2002-12-24T23:59:59.000Z

420

Alkaline and alkaline earth metal phosphate halides and phosphors  

SciTech Connect

Compounds, phosphor materials and apparatus related to nacaphite family of materials are presented. Potassium and rubidium based nacaphite family compounds and phosphors designed by doping divalent rare earth elements in the sites of alkaline earth metals in the nacaphite material families are descried. An apparatus comprising the phosphors based on the nacaphite family materials are presented herein. The compounds presented is of formula A.sub.2B.sub.1-yR.sub.yPO.sub.4X where the elements A, B, R, X and suffix y are defined such that A is potassium, rubidium, or a combination of potassium and rubidium and B is calcium, strontium, barium, or a combination of any of calcium, strontium and barium. X is fluorine, chlorine, or a combination of fluorine and chlorine, R is europium, samarium, ytterbium, or a combination of any of europium, samarium, and ytterbium, and y ranges from 0 to about 0.1.

Lyons, Robert Joseph; Setlur, Anant Achyut; Cleaver, Robert John

2012-11-13T23:59:59.000Z

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


421

Standard test methods for analysis of sintered gadolinium oxide-uranium dioxide pellets  

E-Print Network (OSTI)

1.1 These test methods cover procedures for the analysis of sintered gadolinium oxide-uranium dioxide pellets to determine compliance with specifications. 1.2 The analytical procedures appear in the following order: Section Carbon (Total) by Direct CombustionThermal Conductivity Method C1408 Test Method for Carbon (Total) in Uranium Oxide Powders and Pellets By Direct Combustion-Infrared Detection Method Chlorine and Fluorine by Pyrohydrolysis Ion-Selective Electrode Method C1502 Test Method for Determination of Total Chlorine and Fluorine in Uranium Dioxide and Gadolinium Oxide Gadolinia Content by Energy-Dispersive X-Ray Spectrometry C1456 Test Method for Determination of Uranium or Gadolinium, or Both, in Gadolinium Oxide-Uranium Oxide Pellets or by X-Ray Fluorescence (XRF) Hydrogen by Inert Gas Fusion C1457 Test Method for Determination of Total Hydrogen Content of Uranium Oxide Powders and Pellets by Carrier Gas Extraction Isotopic Uranium Composition by Multiple-Filament Surface-Ioni...

American Society for Testing and Materials. Philadelphia

2006-01-01T23:59:59.000Z

422

Standard test methods for chemical and mass spectrometric analysis of nuclear-grade gadolinium oxide (Gd2O3) powder  

E-Print Network (OSTI)

1.1 These test methods cover procedures for the chemical and mass spectrometric analysis of nuclear-grade gadolinium oxide powders to determine compliance with specifications. 1.2 The analytical procedures appear in the following order: Sections Carbon by Direct CombustionThermal Conductivity C1408 Test Method for Carbon (Total) in Uranium Oxide Powders and Pellets By Direct Combustion-Infrared Detection Method Total Chlorine and Fluorine by Pyrohydrolysis Ion Selective Electrode C1502 Test Method for Determination of Total Chlorine and Fluorine in Uranium Dioxide and Gadolinium Oxide Loss of Weight on Ignition 7-13 Sulfur by CombustionIodometric Titration Impurity Elements by a Spark-Source Mass Spectrographic C761 Test Methods for Chemical, Mass Spectrometric, Spectrochemical,Nuclear, and Radiochemical Analysis of Uranium Hexafluoride C1287 Test Method for Determination of Impurities In Uranium Dioxide By Inductively Coupled Plasma Mass Spectrometry Gadolinium Content in Gadolinium Oxid...

American Society for Testing and Materials. Philadelphia

2006-01-01T23:59:59.000Z

423

Evaluation of environmental-control technologies for commercial nuclear fuel-conversion (UF/sub 6/) facilities  

Science Conference Proceedings (OSTI)

At present in the United States, there are two commercial conversion facilities. These facilities process uranium concentrate into UF/sub 6/ for shipment to the enrichment facilities. One conversion facility uses a dry hydrofluor process, whereas the other facility uses a process known as the wet solvent extraction-fluorination process. Because of the different processes used in the two plants, waste characteristics, quantities, and treatment practices differ at each facility. Wastes and effluent streams contain impurities found in the concentrate (such as uranium daughters, vanadium, molybdenum, selenium, arsenic, and ammonia) and process chemicals used in the circuit (including fluorine, nitrogen, and hydrogen), as well as small quantities of uranium. Studies of suitable disposal options for the solid wastes and sludges generated at the facilities and the long-term effects of emissions to the ambient environment are needed. 30 figures, 34 tables.

Perkins, B.L.

1982-10-01T23:59:59.000Z

424

Interactions between Liquid-Wall Vapor and Edge Plasmas  

DOE Green Energy (OSTI)

The use of liquid walls for fusion reactors could help solve problems associated with material erosion from high plasma heat-loads and neutronic activation of structures. A key issue analyzed here is the influx of impurity ions to the core plasma from the vapor of liquid side-walls. Numerical 2D transport simulations are performed for a slab geometry which approximates the edge region of a reactor-size tokamak. Both lithium vapor (from Li or SnLi walls) and fluorine vapor (from Flibe walls) are considered for hydrogen edge-plasmas in the high- and low-recycling regimes. It is found that the minimum influx is from lithium with a low-recycling hydrogen plasma, and the maximum influx occurs for fluorine with a high-recycling hydrogen plasma.

Rognlien, T D; Rensink, M E

2000-05-25T23:59:59.000Z

425

PROCESS FOR PRODUCING URANIUM HALIDES  

DOE Patents (OSTI)

A process amd associated apparatus for producing UF/sub 4/ from U/sub 3/ O/sub 8/ by a fluidized'' technique are reported. The U/sub 3/O/sub 8/ is first reduced to UO/sub 2/ by reaction with hydrogen, and the lower oxide of uranium is then reacted with gaseous HF to produce UF/sub 4/. In each case the reactant gas is used, alone or in combination with inert gases, to fluidize'' the finely divided reactant solid. The complete setup of the plant equipment including bins, reactor and the associated piping and valving, is described. An auxiliary fluorination reactor allows for the direct production of UF/sub 6/ from UF/sub 4/ and fluorine gas, or if desired, UF/sub 4/ may be collected as the product.

Murphree, E.V.

1957-10-29T23:59:59.000Z

426

Amtsblatt der Europischen Union L 235/1 (Verffentlichungsbedrftige Rechtsakte, die in Anwendung des EG-Vertrags/Euratom-Vertrags erlassen wurden)  

E-Print Network (OSTI)

. Gas Ox. Gas 1 Acute Tox. 2 * Skin Corr. 1B H270 H330 H314 GHS04 GHS03 GHS06 GHS05 Dgr H270 H330 H314-SACremmuN-GEgnunhciezeBehcsimehcelanoitanretnI.rN-xednI #12;AmtsblattderEuropäischenUnionL235/5 009-001-00-0 fluorine 231-954-8 7782-41-4 Press. Gas Ox. Gas 1,5 % C Gas

Kersting, Roland

427

PROCESS FOR PURIFYING CRUDE PERFLUOROCARBONS  

DOE Patents (OSTI)

A method is described for refining organic perfluoro compounds. In the manufacture of perfluorinated compounds by the fluorination of hydrocarbons, the product frequently is contaminated ny incompletely fluorimated hydrogen containing impurities. These impurities can be removed by contacting the products in a fluid conditions with an active adsorbents such as silica gel or alumina gel. The patent claims are restricted to this refining of crude perfluorinated lubricating oil.

Holeton, R.E.

1959-03-24T23:59:59.000Z

428

Method for removal of plutonium impurity from americium oxides and fluorides  

SciTech Connect

Method for removal of plutonium impurity from americium oxides and fluorides. AmF.sub.4 is not further oxidized to AmF.sub.6 by the application of O.sub.2 F at room temperature, while plutonium compounds present in the americium sample are fluorinated to volatile PuF.sub.6, which can readily be separated therefrom, leaving the purified americium oxides and/or fluorides as the solid tetrafluoride.

FitzPatrick, John R. (Los Alamos, NM); Dunn, Jerry G. (Los Alamos, NM); Avens, Larry R. (Los Alamos, NM)

1987-01-01T23:59:59.000Z

429

PROCESS FOR PRODUCTION OF URANIUM HEXAFLUORIDE  

DOE Patents (OSTI)

A process is described for the manufacture of uranium bexafluoride which consists in contacting an oxide of uranium simultaneously with elemental carbon and elemental fluorine at an elevated temperature, using a proportion of the carbon to the oxide about 50% in excess of that theoretically required to combine with f the oxygen as C0/.sub 2/. The process has the advantage that the uranium oxide is reduced by tbe carbon aad converted to the hexafluoride in a single operation.

Fowler, R.D.

1958-11-01T23:59:59.000Z

430

Reactive formulations for a neutralization of toxic industrial chemicals  

DOE Patents (OSTI)

Decontamination formulations for neutralization of toxic industrial chemicals, and methods of making and using same. The formulations are effective for neutralizing malathion, hydrogen cyanide, sodium cyanide, butyl isocyanate, carbon disulfide, phosgene gas, capsaicin in commercial pepper spray, chlorine gas, anhydrous ammonia gas; and may be effective at neutralizing hydrogen sulfide, sulfur dioxide, formaldehyde, ethylene oxide, methyl bromide, boron trichloride, fluorine, tetraethyl pyrophosphate, phosphorous trichloride, arsine, and tungsten hexafluoride.

Tucker, Mark D. (Albuqueruqe, NM); Betty, Rita G. (Rio Rancho, NM)

2006-10-24T23:59:59.000Z

431

CONTINUOUS PROCESS FOR THE CONVERSION OF UF$sub 6$ TO UF$sub 4$  

DOE Patents (OSTI)

A method is presented for reducing UF/sub 6/ to UF/sub 6/ with hydrogen. A preheated mixture of UF/sub 6/ and fluorine is contacted with a stoichiometric excess of preheated hydrogen in a reaction chamber thereby producing UF/sub 6/. The UF/sub 6/ reacts quantitatively and the UF/sub 6/ produced is of high purity and high density.

Smiley, S.H.; Brater, D.C.; Nimmo, R.H.

1959-10-01T23:59:59.000Z

432

Phospho-gypsum recovery process  

SciTech Connect

This patent describes a process for treating phospho-gypsum waste product which is produced in the manufacture of phosphoric acid by the wet-acid process in which suitable phosphate rock is treated with sulforic acid to product phosphoric acid and in which a mixture of phospho-gypsum waste product and carbonaceous material is heated to produce gaseous SO/sub 2/, P/sub 2/O/sub 5/ containing materials and HF containing materials. The improvement comprises drying a mixture of phospho-gypsum waste product and carbonaceous material, removing a first gaseous stream containing water, acids and fluorine, separating the fluorine from the first gaseous stream by reacting with lime or limestone to produce fluorspar, recovering the fluorspar, calcining the dried phospho-gypsum under reducing conditions to produce a second gaseous stream containing SO/sub 2/, CO/sub 2/, O/sub 2/ and N/sub 2/ with substantially no fluorine values, and utilizing the second gaseous stream in a sulfuric acid manufacturing plant.

Wilson, E.K. Sr.; Spigolon, S.J.

1988-03-29T23:59:59.000Z

433

Transparent Conductors and Barrier Layers for Thin Film Solar Cells:  

DOE Green Energy (OSTI)

This report describes the research undertaken to increase the efficiency of thin-film solar cells based on amorphous silicon in the so-called''superstrate structure'' (glass front surface/transparent electrically conductive oxide (TCO)/pin amorphous silicon/metal back electrode). The TCO layer must meet many requirements: high optical transparency in the wavelength region from about 350 to 900 nm, low electrical sheet resistance, stability during handling and deposition of the subsequent layers and during use, a textured (rough) surface to enhance optical absorption of red and near-infrared light, and low-resistance electrical contact to the amorphous silicon p-layer. Fluorine-doped tin oxide has been the TCO used in most commercial superstrate amorphous silicon cells. Fluorine-doped zinc oxide (ZnO:F) was later shown to be even more transparent than fluorine-doped tin oxide, as well as being more resistant to the strongly reducing conditions encountered during the deposition of amorphous silicon. Solar cells based on ZnO:F showed the expected higher currents, but the fill factors were lower than standard cells grown on tin oxide, resulting in no consistent improvement in efficiency. This problem was recently mitigated by using a new proprietary p/buffer layer combination developed at BP Solar.

Gordon, R. G.; Broomhall-Dillard, R.; Liu, X.; Pang, D.; Barton, J.

2001-12-01T23:59:59.000Z

434

Chain Elongation during Thermolysis of Tetrafluoroethylene and Hexafluoropropylene: Modeling of Mechanistic Hypotheses and Elucidation of Data Needs  

SciTech Connect

Thermolysis of tetrafluoroethylene at 500 oC is well-known to lead to equilibration with octafluorocyclobutane; at 600 oC this mixture forms hexafluoropropylene; and at slightly more forcing conditions the latter is converted to octafluoroisobutylene (and/or octafluoro-2-butene). This chain-elongation behavior contrasts with the familiar cracking of non-fluorinated olefins and the thermodynamic rationale is provided herein. Several mechanisms have been proposed in the literature without a clear choice. Kinetic modeling herein of available product/kinetic data with use of current thermochemical and kinetic parameters supports a key role for difluorocarbene formed from dissociation of tetrafluoroethylene. Arbitrary selection between unfortunately inconsistent available measurements and/or computations of elementary rate constants, with modest adjustments, allowed data matches with either a direct insertion into an olefinic C-F bond or an addition to the olefin to give a 1,3-biradical followed by a 1,2-fluorine shift. In contrast, a 1,2-fluorine shift in the starting olefin to generate a carbene, followed by carbene combination, seems unlikely. However, the modeling was only a limited success, especially for hexafluoropropylene as feed which seems a comparatively inefficient source of difluorocarbene. This highlights the need for improved experimental thermolysis data at low conversion, independent elementary rate constants for key steps, and especially enthalpies of formation of fluorocarbons and their reactive intermediates.

Poutsma, Marvin L [ORNL

2011-01-01T23:59:59.000Z

435

(Polyfluoroaryl) fluoroanions of aluminum, gallium, and indium of enhanced utility, uses thereof, and products based thereon  

DOE Patents (OSTI)

The (polyfluoroaryl)fluoroanions of aluminum, gallium, and indium are novel weakly coordinating anions which are highly fluorinated. (Polyfluoroaryl)fluoroanions of one such type contain at least one ring substituent other than fluorine. These (polyfluoroaryl)fluoroanions of aluminum, gallium, and indium have greater solubility in organic solvents, or have a coordinative ability essentially equal to or less than that of the corresponding (polyfluoroaryl)fluoroanion of aluminum, gallium, or indium in which the substituent is replaced by fluorine. Another type of new (polyfluoroaryl)fluoroanion of aluminum, gallium, and indium have 1-3 perfluorinated fused ring groups and 2-0 perfluorophenyl groups. When used as a cocatalyst in the formation of novel catalytic complexes with d- or f-block metal compounds having at least one leaving group such as a methyl group, these anions, because of their weak coordination to the metal center, do not interfere in the ethylene polymerization process, while affecting the propylene process favorably, if highly isotactic polypropylene is desired. Thus, the (polyfluoroaryl)fluoroanions of aluminum, gallium, and indium of this invention are useful in various polymerization processes such as are described.

Marks, Tobin J. (Evanston, IL); Chen, You-Xian (Midland, MI)

2001-01-01T23:59:59.000Z

436

(Polyfluoroaryl)fluoroanions of aluminum, gallium, and indium of enhanced utility, uses thereof, and products based thereon  

DOE Patents (OSTI)

The (polyfluoroaryl)fluoroanions of aluminum, gallium, and indium are novel weakly coordinating anions which are are highly fluorinated. (Polyfluoroaryl)fluoroanions of one such type contain at least one ring substituent other than fluorine. These (polyfluoroaryl)fluoroanions of aluminum, gallium, and indium have greater solubility in organic solvents, or have a coordinative ability essentially equal to or less than that of the corresponding (polyfluoroaryl)fluoroanion of aluminum, gallium, or indium in which the substituent is replaced by fluorine. Another type of new (polyfluoroaryl)fluoroanion of aluminum, gallium, and indium have 1-3 perfluorinated fused ring groups and 2-0 perfluorophenyl groups. When used as a cocatalyst in the formation of novel catalytic complexes with d- or f-block metal compounds having at least one leaving group such as a methyl group, these anions, because of their weak coordination to the metal center, do not interefere in the ethylene polymerization process, while affecting the the propylene process favorably, if highly isotactic polypropylene is desired. Thus, the (polyfluoroaryl)fluoroanions of aluminum, gallium, and indium of this invention are useful in various polymerization processes such as are described.

Marks, Tobin J. (Evanston, IL); Chen, You-Xian (Midland, MI)

2001-01-01T23:59:59.000Z

437

(Polyfluoroaryl) fluoroanions of aluminum, gallium, and indium of enhanced utility, uses thereof, and products based thereon  

DOE Patents (OSTI)

The (polyfluoroaryl)fluoroanions of aluminum, gallium, and indium are novel weakly coordinating anions which are highly fluorinated. (Polyfluoroaryl)fluoroanions of one such type contain at least one ring substituent other than fluorine. These (polyfluoroaryl)fluoroanions of aluminum, gallium, and indium have greater solubility in organic solvents, or have a coordinative ability essentially equal to or less than that of the corresponding (polyfluoroaryl)fluoroanion of aluminum, gallium, or indium in which the substituent is replaced by fluorine. Another type of new (polyfluoroaryl)fluoroanion of aluminum, gallium, and indium have 1-3 perfluorinated fused ring groups and 2-0 perfluorophenyl groups. When used as a cocatalyst in the formation of novel catalytic complexes with d- or f-block metal compounds having at least one leaving group such as a methyl group, these anions, because of their weak coordination to the metal center, do not interfere in the ethylene polymerization process, while affecting the propylene process favorably, if highly isotactic polypropylene is desired. Thus, the (polyfluoroaryl)fluoroanions of aluminum, gallium, and indium of this invention are useful in various polymerization processes such as are described.

Marks, Tobin J. (Evanston, IL); Chen, You-Xian (Midland, MI)

2002-01-01T23:59:59.000Z

438

Baca geothermal demonstration project baseline ecosystem studies of cooling tower emission effects  

DOE Green Energy (OSTI)

Results of baseline studies for boron, arsenic, mercury, and fluorine in vegetation and soil near the Baca Geothermal Demonstration Power Plant are provided for the 1980 sampling season. Preliminary results of visual vegetation assessments and population density studies of soil invertebrate fauna are also provided. Foliage samples were collected for chemical analysis on a total of 17 plots on 5 transects. Two to five plant species were sampled at each plot. Samples were collected in June-July and September. Soil samples were collected at each plot during September. Visual vegetation inspections were conducted along each transect. Eighty-eight soil samples were collected for soil invertebrate studies. Boron, arsenic, mercury, and fluorine levels in vegetation were within normal range for natural vegetation and crops. Concentrations of soil arsenic and mercury were comparable to foliage concentrations. Boron concentrations were lower in soil than in foliage, whereas soil fluorine concentrations were considerably higher than foliage concentrations. With the exception of heavy insect infestations in June-July, no vegetation abnormalities were noted. Preliminary soil invertebrate analysis indicated an overall arthropod density of approximately 100,000/m/sup 2/ which appears within the normal range encountered in forest and meadow soil.

Leitner, P.; Osterling, R.; Price, D.; Westermeier, J.

1981-03-01T23:59:59.000Z

439

HIGH TEMPERATURE CORROSION STUDY INTERIM REPORT FOR THE PERIOD NOVEMBER 1958 THROUGH MAY 1959  

SciTech Connect

Samples of grade A Monel snd grade A nickel were subjected statically in a single reactor to an undiluted atmosphere of gaseous fluorine at pressures up to one atmosphere absolute and temperatures up to 1500 deg F. The grade A Monel was conservatively estimated to have consumed at least 40 times as much fluorine as grade A nickel during the entire period of the investigation. Samples of fused alpha Al/sub 2/O/sub 3/, alpha -Al/sub 2/O/sub 3/- MgO spinel, and alpha -Al/sub 2/O/sub 3/-NiO--nickel cermet were exposed to undiluted fluorine at one atinosphere absolute pressure at temperatures of 1340 and 1500 deg F. Results indicated that the alpha -Al/sub 2/O/sub 3/ is as good as the Ni in the region of 1300 deg F. Grade A nickel samples coated with nickel fluoride filins of 37,000 and 74,000 A, respectively, were exposed to an absolute pressure of gaseous UF/sub 6/ of 12 cm of Hg at temperatures of 1000 and 1800 deg F. (W.L.H.)

Hale, C.F.; Barber, E.J.; Bernhardt, H.A.; Rapp, K.E.

1959-07-28T23:59:59.000Z

440

PROCESS FOR SEPARATING URANIUM FISSION PRODUCTS  

DOE Patents (OSTI)

The removal of fission products such as strontium, barium, cesium, rubidium, or iodine from neutronirradiated uranium is described. Uranium halide or elemental halogen is added to melted irradiated uranium to convert the fission products to either more volatile compositions which vaporize from the melt or to higher melting point compositions which separate as solids.

Spedding, F.H.; Butler, T.A.; Johns, I.B.

1959-03-10T23:59:59.000Z

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


441

40 CFR Ch. I (7105 Edition) 190.10 period in which he is engaged in car-  

E-Print Network (OSTI)

or emissions therefrom and car- rying out inspection and enforcement activities to assure compliance.10(a) shall be effective December 1, 1979, except that for doses arising from operations associated) shall be effective December 1, 1979, except that the standards for krypton-85 and iodine-129 shall

442

Chemical and Physical Investigation of Secondary Organic Aerosol Formation  

E-Print Network (OSTI)

iodine-containing species (IO, OIO, INO3, (IO)2, I2O3, I2O4channel and ~40% for the OIO forming channel (Saiz-Lopez etiodine oxide species, such as OIO, I 2 O 3 , I 2 O 4 , and I

Nakao, Shunsuke

2012-01-01T23:59:59.000Z

443

Pacific Cod  

Science Conference Proceedings (OSTI)

Physical Characteristics of Oils, Fats, and Waxes Cod, Pacific Specific Gravity (SG) 15.5/15.5°C 25/25°C Other SG Refractive Index (RI) 25°C 40°C Other RI Iodine Value Saponification Value Titer °C % Unsaponifiable Melti

444

Features of coal dust dynamics at action of differently oriented forces in granular filtering medium  

E-Print Network (OSTI)

The process of the coal dust particles transportation and structurization in the experimental horizontal model of air filter with the cylindrical coal adsorbent granules as in the iodine air filter at the nuclear power plant is researched. In the investigated case the vector of carrying away force of air flow and the vector of gravitation force are mutually perpendicular, and the scattering of the dust particles on the granules occurs in the normal directions. It is found that the phenomenon of non controlled spontaneous sharp increase of aerodynamic resistance in the iodine air filter under the big integral volumes of filtered air and the big masses of introduced coal dust particles is not observed at the described experimental conditions in distinction from the case of the parallel orientation of this forces as in the vertical iodine air filters at the nuclear power plant. The quantitative measurements of the main parameters of the process of the dust masses transportation and structurization are made on a developed experimental model of the iodine air filter with the cylindrical coal adsorbent granules.

I. M. Neklyudov; L. I. Fedorova; P. Ya. Poltinin; O. P. Ledenyov

2013-01-24T23:59:59.000Z

445

Electronic cleansing in CT colonography: past, present, and future  

Science Conference Proceedings (OSTI)

Fecal tagging is a means of ‘marking' fecal residues (stool and fluid) in a colon by use of the oral administration of a positive contrast agent (barium or iodine) in CT Colonography (CTC). Electronic cleansing (EC) is an emerging technique for ... Keywords: CT colonography, bowel preparation, electronic cleansing, fecal tagging

Wenli Cai; Hiroyuki Yoshida

2010-09-01T23:59:59.000Z

446

Design of GA thermochemical water-splitting process for the Mirror Advanced Reactor System  

DOE Green Energy (OSTI)

GA interfaced the sulfur-iodine thermochemical water-splitting cycle to the Mirror Advanced Reactor System (MARS). The results of this effort follow as one section and part of a second section to be included in the MARS final report. This section describes the process and its interface to the reactor. The capital and operating costs for the hydrogen plant are described.

Brown, L.C.

1983-04-01T23:59:59.000Z

447

Fate of soluble uranium in the I{sub 2}/KI leaching process for mercury removal  

SciTech Connect

General Electric Corporation has developed an extraction and recovery system for mercury, based upon the use of iodine (oxidant) and iodide ion (complexing agent). This system has been proposed for application to select mercury-contaminated mixed waste (i.e., waste containing radionuclides as well as other hazardous constituents), which have been generated by historic activities in support of US Department of Energy (DOE) missions. This system is compared to a system utilizing hypochlorite and chloride ions for removal of mercury and uranium from a sample of authentic mixed waste sludge. Relative to the hypochlorite (bleach) system, the iodine system mobilized more mercury and less uranium from the sludge. An engineering flowsheet has been developed to treat spent iodine-containing extraction medium, allowing the system to be recycled. The fate of soluble uranium in this series of treatment unit operations was monitored by tracing isotopically-enriched uranyl ion into simulated spent extraction medium. Treatment with use of elemental iron is shown to remove > 85% of the traced uranium while concurrently reducing excess iodine to the iodide ion. The next unit operation, adjustment of the solution pH to a value near 12 by the addition of lime slurry to form a metal-laden sludge phase (an operation referred to as lime-softening), removed an additional 57% of soluble uranium activity, for an over-all removal efficiency of {approximately} 96%. However, the precipitated solids did not settle well, and some iodide reagent is held up in the wet filtercake.

Bostick, W.D.; Davis, W.H.; Jarabek, R.J. [East Tennessee Technology Park, Oak Ridge, TN (United States). Materials and Chemistry Lab.

1997-09-01T23:59:59.000Z

448

PRODUCTION OF METALS  

DOE Patents (OSTI)

A process is described producing metallic thorium, titanium, zirconium, or hafnium from the fluoride. In the process, the fluoride is reduced with alkali or alkaline earth metal and a booster compound (e.g. iodine or a decomposable oxysalt) in a sealed bomb at superatmospheric pressure and a temperature above the melting point of the metal to be produced.

Spedding, F.H.; Wilhelm, H.A.; Keller, W.H.

1961-09-19T23:59:59.000Z

449

NHI-Acid Concentration Membranes -- Membrane Recommendations for the S-I Cycle  

DOE Green Energy (OSTI)

Scope: The purpose of this draft report is to make recommendations concerning the applicability of specific membrane materials for acid concentration processes to the Sulfur-Iodine (S-I) thermochemical cycle integrated laboratory scale (ILS) demonstration. Introduction Acid concentration membrane processes have been studied for possible inclusion in the Sulfur-Iodine integrated laboratory scale (S-I ILS) demonstration. The need for this technology is driven by the chemical processes required for economical water splitting using the S-I cycle. Of the chemical processes inherent to the S-I cycle that have been identified as targets for deployment of membrane technology, three have been studied during the past three fiscal years as a part of the DOE Nuclear Hydrogen Initiative. First, the ability to concentrate hydriodic acid (HI) and iodine mixtures was sought as a method for aiding in the isolation of HI away from water and iodine. Isolated HI would then be delivered to the HI decomposition process for liberation of product hydrogen. Second, an extension of this technology to sulfuric acid was proposed to benefit sulfuric acid decomposition recycle. Third, decomposition of HI to form hydrogen is equilibrium limited. Removal of hydrogen, utilizing Le Chatelier’s principle, will increase to overall conversion and thus increasing the efficiency of the S-I cycle.

Frederick F Stewart

2007-03-01T23:59:59.000Z

450

GEER Program & Abstracts  

E-Print Network (OSTI)

-3 2.3 The Protective Action Guides 2-4 2.3.1 Evacuation and Sheltering 2-5 2.3.2 Thyroid and Skin to a 5 rem Thyroid Dose Equivalent from Inhalation of Radioiodine 5-15 5-3 Dose Conversion Factors (DCF plans include procedures for issuing stable iodine to reduce thyroid dose (FE-85), this may

Watson, Craig A.

451

Radioiodinated glucose analogues for use as imaging agents  

DOE Patents (OSTI)

A radioiodinated branched carbohydrate for tissue imaging. Iodine-123 is stabilized in the compound by attaching it to a vinyl functional group that is on the carbohydrate. The compound exhibits good uptake and retention and is promising in the development of radiopharmaceuticals for brain, heart and tumor imaging.

Goodman, Mark M. (Knoxville, TN); Knapp, Jr., Furn F. (Oak Ridge, TN)

1988-01-01T23:59:59.000Z

452

Radioiodinated branched carbohydrates  

DOE Patents (OSTI)

A radioiodinated branched carbohydrate for tissue imaging. Iodine-123 is stabilized in the compound by attaching it to a vinyl functional group that is on the carbohydrate. The compound exhibits good uptake and retention and is promising in the development of radiopharmaceuticals for brain, heart and tumor imaging.

Goodman, Mark M. (Knoxville, TN); Knapp, Jr., Furn F. (Oak Ridge, TN)

1989-01-01T23:59:59.000Z

453

Halogenation of cobalt dicarbollide  

DOE Patents (OSTI)

A method for selectively adding chlorine, bromine, or iodine to cobalt dicarbollide anions by means of electrophilic substitution reactions. Halogens are added only to the B10 and B10' positions of the anion. The process involves use of hypohalous acid or N-halosuccinimide or gaseous chlorine in the presence of iron.

Hurlburt, Paul K. (Los Alamos, NM); Abney, Kent D. (Los Alamos, NM); Kinkead, Scott A. (Los Alamos, NM)

1997-01-01T23:59:59.000Z

454

Written and Printed Sources for the Study of Mongolian Medicine  

E-Print Network (OSTI)

for the operation. This area is to be thoroughly cleaned from the centre outwards with colton wool soaked in iodine, followed by a similar cleansing with spirit. The next section deals with what conditions may be treated by bleeding, and those where...

Bawden, Charles

1993-01-01T23:59:59.000Z

455

Resonance Raman Study of I2 -Intercalated Single-Walled Carbon Nanotubes  

Science Conference Proceedings (OSTI)

We conducted resonance Raman studies on the iodine-intercalated bundles of single-walled carbon nanotubes (SWNTs). The Raman spectra obtained using the 647.1-nm line of a Kr-ion laser indicate that I2 intercalation affects the electronic ... Keywords: I $_2$-intercalation, Raman spectroscopy, resonance Raman, single-walled carbon nanotubes

V. M. Nguyen; I. S. Yang; Y. Jung; S. -J. Kim; J. Oh; W. Yi

2007-01-01T23:59:59.000Z

456

Tracer Studies at Los Alamos 266 Los Alamos Science Number 23 1995  

E-Print Network (OSTI)

the Sec- ond World War, the scientific community split into two groups on the issue of radioactive fallout Project Sunshine, the Atomic Energy Commission funded the various national laboratories to study fallout. Along with strontium-90 and cesium-137, iodine-131 ended up being one of the most studied fallout

Massey, Thomas N.

457

Laser-fusion program. Semiannual report, January--June 1973  

SciTech Connect

Brief discussions are given for each of the following areas of research covered during this report period: solid-state laser program, design analysis, component development, diagnostics, gas lasers, chemical lasers---the iodine laser, basic studies and advanced concepts, laser propagation, laser plasmas, laser fusion, isotope separation, and program resources. (MOW)

Sussman, S.S. (ed.)

1973-08-22T23:59:59.000Z

458

Mercuric iodate precipitation from radioiodine-containing off-gas scrubber solution  

DOE Patents (OSTI)

Mercuric nitrate-nitric acid scrub solutions containing radioiodine may be reduced in volume without excessive loss of volatile iodine. The use of concentrated nitric acid during an evaporation process oxidizes the mercury-iodide complex to a less volatile mercuric iodate precipitate.

Partridge, Jerry A. (Richland, WA); Bosuego, Gail P. (Richland, WA)

1982-01-01T23:59:59.000Z

459

DOI: 10.1126/science.1059011 , 479 (2001);292Science  

E-Print Network (OSTI)

of a (MoS2)-Ix bundle. (A) Hexagonal structure of the tubes within a bundle. (B) High-resolution view- tubes, creating one-dimensional rows along the bundle axis. The periodicity of feasible sites for iodine-diameter molybdenum disulfide tubes. The nanotubes are up to hundreds of micrometers long and display diverse self

460

Hydriodic acid-anode-depolarized hydrogen generator  

SciTech Connect

Hydrogen is recovered from aqueous hydriodic acid in the presence of sulfuric acid, in an electrolysis cell having an anode and cathode compartment separated by a hydrogen ion permeable membrane, by electrochemically liberating iodine in the anode compartment by anodization of iodide anions, and electrochemically generating hydrogen in the cathode compartment from hydrogen cations that migrate across the membrane.

Maskalick, N.J.

1984-07-17T23:59:59.000Z

Note: This page contains sample records for the topic "fluorine iodine phos" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


461

Molecular Level Characterization and Mobility of Radionuclide-Carrying Natural Organic Matter in Aquatic Environments  

E-Print Network (OSTI)

Radionuclides, 129I and 239,240Pu, are major products or by-products of nuclear fission and among the top risk drivers for waste disposal at the Savannah River Sites (SRS) and Rocky Flats Environmental Technology Sites (RFETS), respectively, due to their perceived mobility in the environment, excessive inventory, toxicity, and long half-life. The objective of this study is to investigate the role of natural organic matter in retarding or facilitating the migration of 129I and 239,240Pu in the Department of Energy (DOE) sites. Measurements of 127I and 129I in humic acids (HAs) and fulvic acids (FAs) obtained by five successive alkaline, two glycerol and one citric acid-alkaline extractions, demonstrated that these extractable humic substances (HS) together account for 54-56 percent and 46 percent of the total 127I and 129I in the soil, respectively. The variations among 127I and 129I concentrations, isotopic ratios (129I/127I), chemical properties of all these humic substances indicated iodine was bound to a small-size aromatic subunit (~10 kDa), while the large-size subunit (~90 kDa), which likely linked the small-size unit through some weak chemical forces, determined the relative mobility of iodine bound to organic matter. Soil resuspension experiments simulating surface runoff or stormflow and erosion events were conducted with soils collected from SRS. Results showed that 72-77 percent of the newly-introduced I- or IO3- were irreversibly sequestered into the organic-rich soil, while the rest was transformed into colloidal and dissolved organo-iodine by the soil. The resulting iodine remobilization contradicts the conventional view that considers only I- or IO3- as the mobile forms. Quantitative structure analysis by 13C DPMAS NMR and solution state 1H NMR on these humic substances indicate that iodine is closely related to the aromatic regions containing esterified products of phenolic and fomic acid or other aliphatic carboxylic acids, amide functionalities, quinone-like structure activated by electron-donating groups (e.g., NH2) or hemicelluloses-lignin-like complex with phenyl-glycosidic linkage. The micro-molecular environment, such as the hydrophobic aliphatic periphery hindering the active aromatic cores and the hydrophilic polysaccharides favoring its accessibility towards hydrophilic iodine species, play another key role in the interactions between iodine and SOM. NMR spectra of the colloidal organic Pu carrier which can potentially be released from the soil during the surface runoff or stormflow showed Pu was transported, at sub-pM concentrations, by a cutin-derived soil degradation products containing siderophore-like moieties and virtually all mobile Pu.

Xu, Chen

2011-08-01T23:59:59.000Z

462

SULFUR HEXAFLUORIDE TREATMENT OF USED NUCLEAR FUEL TO ENHANCE SEPARATIONS  

SciTech Connect

Reactive Gas Recycling (RGR) technology development has been initiated at Savannah River National Laboratory (SRNL), with a stretch-goal to develop a fully dry recycling technology for Used Nuclear Fuel (UNF). This approach is attractive due to the potential of targeted gas-phase treatment steps to reduce footprint and secondary waste volumes associated with separations relying primarily on traditional technologies, so long as the fluorinators employed in the reaction are recycled for use in the reactors or are optimized for conversion of fluorinator reactant. The developed fluorination via SF{sub 6}, similar to the case for other fluorinators such as NF{sub 3}, can be used to address multiple fuel forms and downstream cycles including continued processing for LWR via fluorination or incorporation into a aqueous process (e.g. modified FLUOREX) or for subsequent pyro treatment to be used in advanced gas reactor designs such metal- or gas-cooled reactors. This report details the most recent experimental results on the reaction of SF{sub 6} with various fission product surrogate materials in the form of oxides and metals, including uranium oxides using a high-temperature DTA apparatus capable of temperatures in excess of 1000{deg}C . The experimental results indicate that the majority of the fission products form stable solid fluorides and sulfides, while a subset of the fission products form volatile fluorides such as molybdenum fluoride and niobium fluoride, as predicted thermodynamically. Additional kinetic analysis has been performed on additional fission products. A key result is the verification that SF{sub 6} requires high temperatures for direct fluorination and subsequent volatilization of uranium oxides to UF{sub 6}, and thus is well positioned as a head-end treatment for other separations technologies, such as the volatilization of uranium oxide by NF{sub 3} as reported by colleagues at PNNL, advanced pyrochemical separations or traditional full recycle approaches. Based on current results of the research at SRNL on SF{sub 6} fluoride volatility for UNF separations, SF{sub 6} treatment renders all anticipated volatile fluorides studied to be volatile, and all non-volatile fluorides studied to be non-volatile, with the notable exception of uranium oxides. This offers an excellent opportunity to use this as a head-end separations treatment process because: 1. SF{sub 6} can be used to remove volatile fluorides from a UNF matrix while leaving behind uranium oxides. Therefore an agent such as NF{sub 3} should be able to very cleanly separate a pure UF{sub 6} stream, leaving compounds in the bottoms such as PuF{sub 4}, SrF{sub 2} and CsF after the UNF matrix has been pre-treated with SF{sub 6}. 2. Due to the fact that the uranium oxide is not separated in the volatilization step upon direct contact with SF{sub 6} at moderately high temperatures (? 1000{deg}C), this fluoride approach may be wellsuited for head-end processing for Gen IV reactor designs where the LWR is treated as a fuel stock, and it is not desired to separate the uranium from plutonium, but it is desired to separate many of the volatile fission products. 3. It is likely that removal of the volatile fission products from the uranium oxide should simplify both traditional and next generation pyroprocessing techniques. 4. SF{sub 6} treatment to remove volatile fission products, with or without treatment with additional fluorinators, could be used to simplify the separations of traditional aqueous processes in similar fashion to the FLUOREX process. Further research should be conducted to determine the separations efficiency of a combined SF{sub 6}/NF{sub 3} separations approach which could be used as a stand-alone separations technology or a head-end process.

Gray, J.; Torres, R.; Korinko, P.; Martinez-Rodriguez, M.; Becnel, J.; Garcia-Diaz, B.; Adams, T.

2012-09-25T23:59:59.000Z

463

Natural Organic Matter (NOM) in Aquatic Systems: Interactions with Radionuclides (234Th (IV), 129 I) and Biofilms  

E-Print Network (OSTI)

A series of laboratory and field investigations were carried out to elucidate the importance of natural organic matter in aquatic systems, i.e., trace element scavenging (e.g., 234Th) by exopolymeric substances (EPS), formation of biofilms, as well as interactions with 129I. A method involving cross flow ultrafiltration, followed by a three-step cartridge soaking and stirred-cell diafiltration, was developed for isolating EPS from phytoplankton cultures, especially in seawater media. EPS isolated from a marine diatom, Amphora sp. was then subjected to semi-quantitative (e.g., carbohydrate, proteins) and quantitative analysis (e.g., neutral sugars, acidic sugars, sulfate). It appeared that Th (IV) binding by EPS was dominated by the acidic polysaccharides of fraction. For EPS of biofilms collected from polluted streams, hydrophobic proteins were the most abundant components in EPS, followed by more hydrophilic carbohydrates. However, chemical composition of carbohydrates or proteins, i.e., monosaccharides and amino acids, respectively, varied with environmental conditions and substrata applied, which suggests that the formation of biofilms on different substrates is regulated by specific properties of microorganisms, environmental conditions and nature of substratum. No correlation between relative hydrophobicity of substratum and development of biofilm was found in this study. A sensitive and rapid GC-MS method was developed to enable the determination of isotopic ratios (129I/127I) of speciated iodine in natural waters. At the F-area of the Savannah River Site (SRS), iodine species in the groundwater consisted of 48.8 percent iodide, 27.3 percent iodate and 23.9 percent organo-iodine. Each of these iodine species exhibited vastly different transport behavior in the column experiments using surface soil from the SRS. Results demonstrated that mobility of iodine species depended greatly on the iodine concentration, mostly due to the limited sorptive capacity for anions of the soil. EPS, especially enzymes (e.g., haloperoxidases) could facilitate the incorporation of iodide to natural organic carbon. At high input concentrations of iodate (78.7 ?M), iodate was found to be completely reduced and subsequently followed the transport behavior of iodide. The marked reduction of iodate was probably associated with natural organic carbon and facilitated by bacteria, besides inorganic reductants (e.g., Fe2 ) in sediments and pore water.

Zhang, Saijin

2010-08-01T23:59:59.000Z

464

Segmentation and quantification of materials with energy discriminating computed tomography: A phantom study  

Science Conference Proceedings (OSTI)

Purpose: To experimentally investigate whether a computed tomography (CT) system based on CdZnTe (CZT) detectors in conjunction with a least-squares parameter estimation technique can be used to decompose four different materials. Methods: The material decomposition process was divided into a segmentation task and a quantification task. A least-squares minimization algorithm was used to decompose materials with five measurements of the energy dependent linear attenuation coefficients. A small field-of-view energy discriminating CT system was built. The CT system consisted of an x-ray tube, a rotational stage, and an array of CZT detectors. The CZT array was composed of 64 pixels, each of which is 0.8x0.8x3 mm. Images were acquired at 80 kVp in fluoroscopic mode at 50 ms per frame. The detector resolved the x-ray spectrum into energy bins of 22-32, 33-39, 40-46, 47-56, and 57-80 keV. Four phantoms were constructed from polymethylmethacrylate (PMMA), polyethylene, polyoxymethylene, hydroxyapatite, and iodine. Three phantoms were composed of three materials with embedded hydroxyapatite (50, 150, 250, and 350 mg/ml) and iodine (4, 8, 12, and 16 mg/ml) contrast elements. One phantom was composed of four materials with embedded hydroxyapatite (150 and 350 mg/ml) and iodine (8 and 16 mg/ml). Calibrations consisted of PMMA phantoms with either hydroxyapatite (100, 200, 300, 400, and 500 mg/ml) or iodine (5, 15, 25, 35, and 45 mg/ml) embedded. Filtered backprojection and a ramp filter were used to reconstruct images from each energy bin. Material segmentation and quantification were performed and compared between different phantoms. Results: All phantoms were decomposed accurately, but some voxels in the base material regions were incorrectly identified. Average quantification errors of hydroxyapatite/iodine were 9.26/7.13%, 7.73/5.58%, and 12.93/8.23% for the three-material PMMA, polyethylene, and polyoxymethylene phantoms, respectively. The average errors for the four-material phantom were 15.62% and 2.76% for hydroxyapatite and iodine, respectively. Conclusions: The calibrated least-squares minimization technique of decomposition performed well in breast imaging tasks with an energy resolving detector. This method can provide material basis images containing concentrations of the relevant materials that can potentially be valuable in the diagnostic process.

Le, Huy Q.; Molloi, Sabee [Department of Radiological Sciences, University of California, Irvine, California 92697 (United States)

2011-01-15T23:59:59.000Z

465

PREPARATION OF ANHYDROUS F-18 FLUORIDE, T. Tewson. Journal of Labelled Compounds and Radiopharmaceuticals S165; 52, Supplement 1 2009  

SciTech Connect

The original specific aims of the grant where cut back considerably as the study section reduced both the time and the budget for the project. The objective of the grant was to show that fluorine-18 fluoride could be prepared completely anhydrous and thus substantially more reactive than conventionally dried fluoride using the method of Sun and DiMagno. This method involved using conventionally dried fluoride to prepare an aromatic fluoride in which the aromatic ring is substituted with electron withdrawing groups. The aryl fluoride is then dried and purified and the fluoride is displaced with an anhydrous nucleophile. Using fluorine-19 and macroscopic scale reactions the reactions work well and give anhydrous fluoride salts that are both more reactive and more selective in their reactions than conventionally dried fluoride. The original substrate chosen for the reaction was bromopentacyanobenzene (1). This compound proved to be easy to make but very hard to purify. As an alternative hexabromobenzene, which is commercially available in high purity, was tried. This reacted cleanly with conventionally dried F-18 fluoride in acetonitrile to give [{sup 18}F]-fluoropentabromobenzene (2), which could be dried by passage of the solution over alumina, which also removed any unreacted fluoride. The fluorine-18 fluoride could be liberated from (2) by displacement with an anhydrous nucleophilic tetra-alkylammonium salt but the anion had to be chosen with considerable care. The reaction is potentially reversible especially as, on the no carrier added scale, there is inevitably an excess of hexabromobenzene and so the displacing nucleophile is chosen to deactivate the aromatic compound to further nucleophilic displacement reactions. To this end tetrabutylammonium azide and tetrabutylammonium phenolate have been tried. Both work but the phenolate is probably the better choice. The F-18 fluoride produced by this process is substantially more reactive than conventionally dried fluoride. A solution of the 3'-anhydrothymidine-5-benzoate (3) was added to the fluoride solution and 30% of the fluoride was incorporated in less than 3 minutes at room temperature were as conventionally dried fluoride requires 10 minutes at 160 C and gives {approx}10% incorporation. These results are encouraging in that they show that the objective of truly anhydrous fluoride is worth pursuing but the problem is that you end up with too much 'stuff' in the solution. Four to five milligrams of hexabromobenzene are used for the initial fluorination reaction and enough of the tetra-alkylammonium salt has to be added to react with a substantial number of those bromides. No attempt has been made to optimize these amounts but there is clearly a lot of material in the solution before the final substrate is added. To avoid these difficulties experiments involving a different, low boiling carrier of the fluoride which can be distilled from the initial fluorination mixture have been tried. Phenyltrifluoromethane sulfonate reacts with fluoride to give trifluoromethane sulfonyl fluoride which boils at -20 C as shown. This reaction works with conventionally dried fluorine-18 fluoride and the no carrier added trifluoromethane sulphonyl fluoride distills out of the reaction as it forms. The choice of nucleophile to react it with to liberate the fluoride is limited and the obvious choice is tetrabutylammonium azide as the resulting trifluoromethane sulfonyl azide is unreactive. We have shown that this works in principle but the experimental details have not been explored.

Tewson, T.

2009-07-01T23:59:59.000Z

466

Identification and characterization of conservative organic tracers for use as hydrologic tracers for the Yucca Mountain site characterization study. Final report  

Science Conference Proceedings (OSTI)

Extensive tracer testing is expected to take place at the C-well complex in the Nevada Test Site as part of the Yucca Mountain Site Characterization Project. The C-well complex consists of one pumping well, C3, and two injection wells, C1 and C2 into which tracer will be introduced. The goal of this research was to provide USGS with numerous tracers to completed these tests. Several classes of fluorinated organic acids have been evaluated. These include numerous isomers of fluorinated benzoic acids, cinnamic acids, and salicylic acids. Also several derivatives of 2-hydroxy nicotinic acid (pyridone) have been tested. The stability of these compounds was determined using batch and column tests. Ames testing (mutagenicity/carcinogenicity) was conducted on the fluorinated benzoic acids and a literature review of toxicity of the fluorobenzoates and three perfluoro aliphatic acids was prepared. Solubilities were measured and method development work was performed to optimize the detection of these compounds. A Quality Assurance (QA) Program was developed under existing DOE and USGS guidelines. The program includes QA procedures and technical standard operating procedures. A tracer test, using sodium iodide, was performed at the C-well complex. HRC chemists performed analyses on site, to provide real time data for the USGS hydrologists and in the laboratories at UNLV. Over 2,500 analyses were performed. This report provides the results of the laboratory experiments and literature reviews used to evaluate the potential tracers and reports on the results of the iodide C-well tracer test.

Stetzenbach, K.; Farnham, I.

1996-06-01T23:59:59.000Z

467

Climate VISION: Private Sector Initiatives: Semiconductors: Resources and  

Office of Scientific and Technical Information (OSTI)

Technical Information Technical Information Download Acrobat Reader Modeling China's Semiconductor Industry Fluorinated Compound Emissions and Drafting a Roadmap for Climate Protection. (PDF 101 KB) 14th Annual International Semiconductor Environment Safety & Health (ISESH) Conference in Jeju, Korea (June 2007) presentation by Scott Bartos, U.S. EPA. Estimating the Impact of Migration to Asian Foundry Production on Attaining the WSC 2010 PFC Reduction Goal. (PDF 458 KB) 11th Annual ISESH Conference in Makuhari, Japan (July 2004) presentation by Scott Bartos, U.S. EPA. Guidelines for Environmental Characterization of Semiconductor Equipment (PDF 361 KB) This document provides guidelines for suppliers of semiconductor processing and abatement equipment to characterize their equipment to meet

468

A PROCESS FOR THE RECOVERY OF URANIUM FROM NUCLEAR FUEL ELEMENTS USING FLUID-BED DRYING AND VOLATILITY TECHNIQUES  

SciTech Connect

A process scheme for the recovery of uranium from fuel elements has been developed. The scheme combines continuous fluid-bed drying and fluoride volatility techniques after initial dissolution of the fuel element in the appropriate aqueous system, hence the designation ADF, Aqueous Dry Fluorination Process. The application of this process to the recovery of uranium from highly enriched, low uranium-zirconium alloy plate-type fuels is described. ln the process, the feed solution is sprayed horizontally through a two-fluid nozzle and is atomized directly in the heated fluidized bed. The spray droplets are dried on the fluidized particles and form a dense coating. Excessive particle growth was limited by the use of air attrition-jets inserted directly in the bed. Aqueous hydrofluoric acid solutions containing l.2 to 3.6 M zirconiuni, 0.007 to 0.03 M uranium, and free acid concentrations from 1 to about l0 M were successfully processed in a 6-in.-diameter Inconel fluid-bed spray dryer. Rates equivalent to about 3.l kg/hr of zirconium were achieved, 160 ml/min with the most concentrated feed solution. Experiments were successfully carried out from 240 to 450 deg C. A new design for a two-fluid nozzle was developed. Extensive work was done to identify the various zirconium fluoride compounds formed. The granular dryer product was subsequently fluorinated at temperatures to 600 deg C in fluid beds and to 700 deg C in static beds to remove the uranium as the volatile hexafluoride. About 90 to 95% uranium removal was consistently achieved near 600 deg C. The relatively low uranium recovery under these conditions is a disadvantage for the application to zirconium-base fuels. It was found necessary to resort to static beds and higher temperatures to achieve greater removal. Since the fluorine attack on nickel, the material of construction, is prohibitive at temperatures above 600 deg C, a disposable fluorinator concept for use with static beds is described. Results of corrosion studies are reported. A preliminary chemical flowsheet with a design capacity of 1l00 kg of uranium (93% enriched) annually is presented. (auth)

Levitz, N.; Barghusen, J.; Carls, E.; Jonke, A.A.

1961-11-01T23:59:59.000Z

469

NEW LABORATORY DEVELOPMENTS IN THE ZIRCEX PROCESS  

SciTech Connect

A new Zircex flowsheet is proposed in which the nonvolatile products from hydrochlorination of uranium-zirconium alloys are chlorinated with carbon tetrachloride, thereby avoiding the loss of 1 to 6% of the uranium observed in engineering development studies of the older flowsheet for STR fuel in which the hydrochlorination residue was dissolved in nitric acid. Other potential advantages of the new flowsheet include decreased corrosion and elimination of possible explosions between uranium--zirconium alloys and nitric acid. The uranium may be recovered by aqueous dissolution and solvent extraction or by gas- phase fluorination at 200 to 400 deg C of uranium chlorides. (auth)

Gens, T.A.; Jolley, R.L.

1961-06-01T23:59:59.000Z

470

Measurement of the 20 and 90 keV Resonances in the {sup 18}O(p,{alpha}){sup 15}N Reaction via the Trojan Horse Method  

SciTech Connect

The {sup 18}O(p,{alpha}){sup 15}N reaction is of primary importance in several astrophysical scenarios, including fluorine nucleosynthesis inside asymptotic giant branch stars as well as oxygen and nitrogen isotopic ratios in meteorite grains. Thus the indirect measurement of the low energy region of the {sup 18}O(p,{alpha}){sup 15}N reaction has been performed to reduce the nuclear uncertainty on theoretical predictions. In particular the strength of the 20 and 90 keV resonances has been deduced and the change in the reaction rate evaluated.

La Cognata, M.; Spitaleri, C.; Cherubini, S.; Crucilla, V.; Gulino, M.; Lamia, L.; Pizzone, R. G.; Puglia, S. M. R.; Rapisarda, G. G.; Romano, S.; Sergi, M. L.; Tumino, A. [INFN Laboratori Nazionali del Sud and DMFCI Universita di Catania, 95123 Catania (Italy); Mukhamedzhanov, A. M.; Tribble, R. E.;