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1

Laser isotope separation  

DOE Patents (OSTI)

A process and apparatus for separating isotopes by selective excitation of isotopic species of a volatile compound by tuned laser light is described. A highly cooled gas of the volatile compound is produced in which the isotopic shift is sharpened and defined. Before substantial condensation occurs, the cooled gas is irradiated with laser light precisely tuned to a desired wavelength to selectively excite a particular isotopic species in the cooled gas. The laser light may impart sufficient energy to the excited species to cause it to undergo photolysis, photochemical reaction or even to photoionize. Alternatively, a two-photon irradiation may be applied to the cooled gas to induce photolysis, photochemical reaction or photoionization. The process is particularly applicable to the separation of isotopes of uranium.

Robinson, C.P.; Reed, J.J.; Cotter, T.P.; Boyer, K.; Greiner, N.R.

1975-11-26T23:59:59.000Z

2

Atomic vapor laser isotope separation  

SciTech Connect

Atomic vapor laser isotope separation (AVLIS) is a general and powerful technique. A major present application to the enrichment of uranium for light-water power reactor fuel has been under development for over 10 years. In June 1985 the Department of Energy announced the selection of AVLIS as the technology to meet the nation's future need for the internationally competitive production of uranium separative work. The economic basis for this decision is considered, with an indicated of the constraints placed on the process figures of merit and the process laser system. We then trace an atom through a generic AVLIS separator and give examples of the physical steps encountered, the models used to describe the process physics, the fundamental parameters involved, and the role of diagnostic laser measurements.

Stern, R.C.; Paisner, J.A.

1985-11-08T23:59:59.000Z

3

Atomic vapor laser isotope separation process  

DOE Patents (OSTI)

A laser spectroscopy system is utilized in an atomic vapor laser isotope separation process. The system determines spectral components of an atomic vapor utilizing a laser heterodyne technique. 23 figs.

Wyeth, R.W.; Paisner, J.A.; Story, T.

1990-08-21T23:59:59.000Z

4

Carbon Isotope Separation and Molecular Formation in Laser-Induced...  

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

Carbon Isotope Separation and Molecular Formation in Laser-Induced Plasmas by Laser Ablation Molecular Isotopic Spectrometry Title Carbon Isotope Separation and Molecular Formation...

5

Laser Isotope Separation Employing Condensation Repression  

SciTech Connect

Molecular laser isotope separation (MLIS) techniques using condensation repression (CR) harvesting are reviewed and compared with atomic vapor laser isotope separation (AVLIS), gaseous diffusion (DIF), ultracentrifuges (UCF), and electromagnetic separations (EMS). Two different CR-MLIS or CRISLA (Condensation Repression Isotope Separation by Laser Activation) approaches have been under investigation at the University of Missouri (MU), one involving supersonic super-cooled free jets and dimer formation, and the other subsonic cold-wall condensation. Both employ mixtures of an isotopomer (e.g. {sup i}QF{sub 6}) and a carrier gas, operated at low temperatures and pressures. Present theories of VT relaxation, dimerization, and condensation are found to be unsatisfactory to explain/predict experimental CRISLA results. They were replaced by fundamentally new models that allow ab-initio calculation of isotope enrichments and predictions of condensation parameters for laser-excited and non-excited vapors which are in good agreement with experiment. Because of supersonic speeds, throughputs for free-jet CRISLA are a thousand times higher than cold-wall CRISLA schemes, and thus preferred for large-quantity Uranium enrichments. For small-quantity separations of (radioactive) medical isotopes, the simpler coldwall CRISLA method may be adequate.

Eerkens, Jeff W.; Miller, William H.

2004-09-15T23:59:59.000Z

6

Laser isotope separation by multiple photon absorption  

DOE Patents (OSTI)

Multiple photon absorption from an intense beam of infrared laser light may be used to induce selective chemical reactions in molecular species which result in isotope separation or enrichment. The molecular species must have a sufficient density of vibrational states in its vibrational manifold that, in the presence of sufficiently intense infrared laser light tuned to selectively excite only those molecules containing a particular isotope, multiple photon absorption can occur. By this technique, for example, intense CO.sub.2 laser light may be used to highly enrich .sup.34 S in natural SF.sub.6 and .sup.11 B in natural BCl.sub.3.

Robinson, C. Paul (Los Alamos, NM); Rockwood, Stephen D. (Los Alamos, NM); Jensen, Reed J. (Los Alamos, NM); Lyman, John L. (Los Alamos, NM); Aldridge, III, Jack P. (Los Alamos, NM)

1977-01-01T23:59:59.000Z

7

Laser isotope separation by multiple photon absorption  

DOE Patents (OSTI)

Multiple photon absorption from an intense beam of infrared laser light may be used to induce selective chemical reactions in molecular species which result in isotope separation or enrichment. The molecular species must have a sufficient density of vibrational states in its vibrational manifold that, is the presence of sufficiently intense infrared laser light tuned to selectively excite only those molecules containing a particular isotope, multiple photon absorption can occur. By this technique, for example, intense CO.sub.2 laser light may be used to highly enrich .sup.34 S in natural SF.sub.6 and .sup.11 B in natural BCl.sub.3.

Robinson, C. Paul (Los Alamos, NM); Rockwood, Stephen D. (Los Alamos, NM); Jensen, Reed J. (Los Alamos, NM); Lyman, John L. (Los Alamos, NM); Aldridge, III, Jack P. (Los Alamos, NM)

1987-01-01T23:59:59.000Z

8

Laser-assisted isotope separation of tritium  

DOE Patents (OSTI)

Methods for laser-assisted isotope separation of tritium, using infrared multiple photon dissociation of tritium-bearing products in the gas phase. One such process involves the steps of (1) catalytic exchange of a deuterium-bearing molecule XYD with tritiated water DTO from sources such as a heavy water fission reactor, to produce the tritium-bearing working molecules XYT and (2) photoselective dissociation of XYT to form a tritium-rich product. By an analogous procedure, tritium is separated from tritium-bearing materials that contain predominately hydrogen such as a light water coolant from fission or fusion reactors.

Herman, Irving P. (Castro Valley, CA); Marling, Jack B. (Livermore, CA)

1983-01-01T23:59:59.000Z

9

Pulsed CO laser for isotope separation of uranium  

SciTech Connect

This article proposes a technical solution for using a CO laser facility for the industrial separation of uranium used in the production of fuel for nuclear power plants, employing a method of laser isotope separation of uranium with condensation repression in a free jet. The laser operation with nanosecond pulse irradiation can provide an acceptable efficiency in the separating unit and a high efficiency of the laser with the wavelength of 5.3 {mu}m. In the present work we also introduce a calculation model and define the parameters of a mode-locked CO laser with a RF discharge in the supersonic stream. The average pulsed CO laser power of 3 kW is sufficient for efficient industrial isotope separation of uranium in one stage.

Baranov, Igor Y.; Koptev, Andrey V. [Rocket-Space Technics Department, Baltic State Technical University, 1, 1st Krasnoarmeyskaya st.,St. Petersburg, 190005 (Russian Federation)

2012-07-30T23:59:59.000Z

10

The Atomic Vapor Laser Isotope Separation Program. [Atomic Vapor Laser Isotope Separation (AVLIS) Program  

SciTech Connect

This report provides the finding and recommendations on the audit of the Atomic Vapor Laser Isotope Separation (AVLIS) program. The status of the program was assessed to determine whether the Department was achieving objectives stated in its January 1990 Plan for the Demonstration, Transition and Deployment of AVLIS Technology. Through Fiscal Year 1991, the Department had spent about $1.1 billion to develop AVLIS technology. The January 1990 plan provided for AVLIS to be far enough along by September to enable the Department to make a determination of the technical and economic feasibility of deployment. However, the milestones needed to support that determination were not met. An estimated $550 million would be needed to complete AVLIS engineering development and related testing prior to deployment. The earliest possible deployment date has slipped to beyond the year 2000. It is recommended that the Department reassess the requirement for AVLIS in light of program delays and changes that have taken place in the enrichment market since January 1990. Following the reassessment, a decision should be made to either fully support and promote the actions needed to complete AVLIS development or discontinue support for the program entirely. Management's position is that the Department will successfully complete the AVLIS technology demonstration and that the program should continue until it can be transferred to a Government corporation. Although the auditors recognize that AVLIS may be transferred, there are enough technical and financial uncertainties that a thorough assessment is warranted.

Not Available

1992-11-09T23:59:59.000Z

11

High-Voltage Power Supply System for Laser Isotope Separation  

SciTech Connect

This report presents several concepts for Laser High-Voltage Power Supply (HVPS) Systems for a Laser Isotope Separation facility. Selection of equipments and their arrangement into operational systems is based on proven designs and on application concepts now being developed. This report has identified a number of alternative system arrangements and has provided preliminary cost estimates for each. The report includes a recommendation for follow-on studies that will further define the optimum Laser HVPS Systems. Brief descriptions are given of Modulator/Regulator circuit trade-offs, system control interfaces, and their impact on costs.

Ketaily, E.C.; Buckner, R.P.; Uhrik, R.L.

1979-06-26T23:59:59.000Z

12

ISOTOPE SEPARATORS  

DOE Patents (OSTI)

An improvement is presented in the structure of an isotope separation apparatus and, in particular, is concerned with a magnetically operated shutter associated with a window which is provided for the purpose of enabling the operator to view the processes going on within the interior of the apparatus. The shutier is mounted to close under the force of gravity in the absence of any other force. By closing an electrical circuit to a coil mouated on the shutter the magnetic field of the isotope separating apparatus coacts with the magnetic field of the coil to force the shutter to the open position.

Bacon, C.G.

1958-08-26T23:59:59.000Z

13

Method for separating boron isotopes  

SciTech Connect

A method of separating boron isotopes .sup.10 B and .sup.11 B by laser-induced selective excitation and photodissociation of BCl.sub.3 molecules containing a particular boron isotope. The photodissociation products react with an appropriate chemical scavenger and the reaction products may readily be separated from undissociated BCl.sub.3, thus effecting the desired separation of the boron isotopes.

Rockwood, Stephen D. (Los Alamos, NM)

1978-01-01T23:59:59.000Z

14

Isotope separation by photochromatography  

DOE Patents (OSTI)

An isotope separation method which comprises physically adsorbing an isotopically mixed molecular species on an adsorptive surface and irradiating the adsorbed molecules with radiation of a predetermined wavelength which will selectively excite a desired isotopic species. Sufficient energy is transferred to the excited molecules to desorb them from the surface and thereby separate them from the unexcited undesired isotopic species. The method is particularly applicable to the separation of hydrogen isotopes.

Suslick, Kenneth S. (Stanford, CA)

1977-01-01T23:59:59.000Z

15

Method for separating isotopes  

DOE Patents (OSTI)

Isotopes are separated by contacting a feed solution containing the isotopes with a cyclic polyether wherein a complex of one isotope is formed with the cyclic polyether, the cyclic polyether complex is extracted from the feed solution, and the isotope is thereafter separated from the cyclic polyether.

Jepson, B.E.

1975-10-21T23:59:59.000Z

16

Laser-induced separation of hydrogen isotopes in the liquid phase  

DOE Patents (OSTI)

Hydrogen isotope separation is achieved by either (a) dissolving a hydrogen-bearing feedstock compound in a liquid solvent, or (b) liquefying a hydrogen-bearing feedstock compound, the liquid phase thus resulting being kept at a temperature at which spectral features of the feedstock relating to a particular hydrogen isotope are resolved, i.e., a clear-cut isotope shift is delineated, irradiating the liquid phase with monochromatic radiation of a wavelength which at least preferentially excites those molecules of the feedstock containing a first hydrogen isotope, inducing photochemical reaction in the excited molecules, and separating the reaction product containing the first isotope from the liquid phase.

Freund, Samuel M. (Los Alamos, NM); Maier, II, William B. (Los Alamos, NM); Beattie, Willard H. (Los Alamos, NM); Holland, Redus F. (Los Alamos, NM)

1980-01-01T23:59:59.000Z

17

I CALCULATIONS ON ISOTOPE SEPARATION BY LASER INDUCED PHOTODISSOCIATION OF POLYATOMIC MOLECULES  

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

; ; . I CALCULATIONS ON ISOTOPE SEPARATION BY LASER INDUCED PHOTODISSOCIATION OF POLYATOMIC MOLECULES F i n a l Report Willis E . Lamb, JY. U n i v e r s i t y of Arizona Tucson, Arizona 85721 NOTICE report was prepared 86 an account of work sponsored by the United Stater Government. Neither the United S t a m nor the United States Department of Encrwi, nor any of their employees, nor any of thelr contractors, Subcontractors, o r their employer, maker any warranty, exprels or Implied. or apumn my k@ liability or responsibility for the aceuraey. eompletencu or uvfulneu of any informtion, apparatus. product Process disclosed. or rtpreYnu that its ur would not infringe privately o m d righu. November 1978 Prepared f o r TIE UNITED STATES DEPARTMENT OF ENERGY Under Contract No. EN-77-S-02--000

18

Isotope separation apparatus and method  

DOE Patents (OSTI)

The invention relates to an improved method and apparatus for laser isotope separation by photodeflection. A molecular beam comprising at least two isotopes to be separated intersects, preferably substantially perpendicular to one broad side of the molecular beam, with a laser beam traveling in a first direction. The laser beam is reflected back through the molecular beam, preferably in a second direction essentially opposite to the first direction. Because the molecules in the beam occupy various degenerate energy levels, if the laser beam comprises chirped pulses comprising selected wavelengths, the laser beam will very efficiently excite substantially all unexcited molecules and will cause stimulated emission of substantially all excited molecules of a selected one of the isotopes in the beam which such pulses encounter. Excitation caused by first direction chirped pulses moves molecules of the isotope excited thereby in the first direction. Stimulated emission of excited molecules of the isotope is brought about by returning chirped pulses traveling in the second direction. Stimulated emission moves emitting molecules in a direction opposite to the photon emitted. Because emitted photons travel in the second direction, emitting molecules move in the first direction. Substantial molecular movement of essentially all the molecules containing the one isotope is accomplished by a large number of chirped pulse-molecule interactions. A beam corer collects the molecules in the resulting enriched divergent portions of the beam.

Feldman, Barry J. (Los Alamos, NM)

1985-01-01T23:59:59.000Z

19

Isotope separation apparatus and method  

DOE Patents (OSTI)

The invention relates to a method and apparatus for laser isotope separation by photodeflection. A molecular beam comprising at least two isotopes to be separated intersects, preferable substantially perpendicular to one broad side of the molecular beam, with a laser beam traveling in a first direction. The laser beam is reflected back through the molecular beam, preferably in a second direction essentially opposite to the first direction. The laser beam comprises .pi.-pulses of a selected wavelength which excite unexcited molecules, or cause stimulated emission of excited molecules of one of the isotopes. Excitation caused by first direction .pi.-pulses moves molecules of the isotope excited thereby in the first direction. Stimulated emission of excited molecules of the isotope is brought about by returning .pi.-pulses traveling in the second direction. Stimulated emission moves emitting molecules in a direction opposite to the photon emitted. Because emitted photons travel in the second direction, emitting molecules move in the first direction. Substantial molecular movement is accomplished by a large number of .pi.-pulse-molecule interactions. A beam corer collects the molecules in the resulting enriched divergent portions of the beam.

Cotter, Theodore P. (Los Alamos, NM)

1982-12-28T23:59:59.000Z

20

Separation of sulfur isotopes  

DOE Patents (OSTI)

Sulfur isotopes are continuously separated and enriched using a closed loop reflux system wherein sulfur dioxide (SO.sub.2) is reacted with sodium hydroxide (NaOH) or the like to form sodium hydrogen sulfite (NaHSO.sub.3). Heavier sulfur isotopes are preferentially attracted to the NaHSO.sub.3, and subsequently reacted with sulfuric acid (H.sub.2 SO.sub.4) forming sodium hydrogen sulfate (NaHSO.sub.4) and SO.sub.2 gas which contains increased concentrations of the heavier sulfur isotopes. This heavy isotope enriched SO.sub.2 gas is subsequently separated and the NaHSO.sub.4 is reacted with NaOH to form sodium sulfate (Na.sub.2 SO.sub.4) which is subsequently decomposed in an electrodialysis unit to form the NaOH and H.sub.2 SO.sub.4 components which are used in the aforesaid reactions thereby effecting sulfur isotope separation and enrichment without objectionable loss of feed materials.

DeWitt, Robert (Centerville, OH); Jepson, Bernhart E. (Dayton, OH); Schwind, Roger A. (Centerville, OH)

1976-06-22T23:59:59.000Z

Note: This page contains sample records for the topic "laser isotope separation" 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

Chromatographic hydrogen isotope separation  

DOE Patents (OSTI)

Intermetallic compounds with the CaCu.sub.5 type of crystal structure, particularly LaNiCo.sub.4 and CaNi.sub.5, exhibit high separation factors and fast equilibrium times and therefore are useful for packing a chromatographic hydrogen isotope separation colum. The addition of an inert metal to dilute the hydride improves performance of the column. A large scale mutli-stage chromatographic separation process run as a secondary process off a hydrogen feedstream from an industrial plant which uses large volumes of hydrogen can produce large quantities of heavy water at an effective cost for use in heavy water reactors.

Aldridge, Frederick T. (Livermore, CA)

1981-01-01T23:59:59.000Z

22

Isotope separation of {sup 17}O by photodissociation of ozone with near-infrared laser irradiation  

Science Conference Proceedings (OSTI)

Oxygen-17 is a stable oxygen isotope useful for various diagnostics in both engineering and medical applications. Enrichment of {sup 17}O, however, has been very costly due to the lack of appropriate methods that enable efficient production of {sup 17}O on an industrial level. In this paper, we report the first {sup 17}O-selective photodissociation of ozone at a relatively high pressure, which has been achieved by irradiating a gas mixture of 10 vol% O{sub 3}-90 vol% CF{sub 4} with narrowband laser. The experiment was conducted on a pilot-plant scale. A total laser power of 1.6 W was generated by external-cavity diode lasers with all the laser wavelengths fixed at the peak of an absorption line of {sup 16}O{sup 16}O{sup 17}O around 1 {mu}m. The beams were introduced into a 25 -m long photoreaction cell under the sealed-off condition with a total pressure of 20 kPa. Lower cell temperature reduced the background decomposition of ozone, and at the temperature of 158 K, an {sup 17}O enrichment factor of 2.2 was attained.

Hayashida, Shigeru; Kambe, Takashi; Sato, Tetsuya; Igarashi, Takehiro [Tsukuba Laboratories, Taiyo Nippon Sanso Corporation, 10 Okubo Tsukuba-shi, Ibaraki 300-2611 (Japan); Kuze, Hiroaki [Center for Environmental Remote Sensing, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba, 263-8522 (Japan)

2012-04-01T23:59:59.000Z

23

Hybrid isotope separation scheme  

DOE Patents (OSTI)

A method of yielding selectively a desired enrichment in a specific isotope including the steps of inputting into a spinning chamber a gas from which a scavenger, radiating the gas with a wave length or frequency characteristic of the absorption of a particular isotope of the atomic or molecular gas, thereby inducing a photochemical reaction between the scavenger, and collecting the specific isotope-containing chemical by using a recombination surface or by a scooping apparatus.

Maya, Jakob (Brookline, MA)

1991-01-01T23:59:59.000Z

24

Method of separating boron isotopes  

SciTech Connect

A method of boron isotope enrichment involving the isotope preferential photolysis of (2-chloroethenyl)dichloroborane as the feed material. The photolysis can readily be achieved with CO.sub.2 laser radiation and using fluences significantly below those required to dissociate BCl.sub.3.

Jensen, Reed J. (Los Alamos, NM); Thorne, James M. (Provo, UT); Cluff, Coran L. (Provo, UT); Hayes, John K. (Salt Lake City, UT)

1984-01-01T23:59:59.000Z

25

Hydrogen isotope separation  

DOE Patents (OSTI)

A system of four cryogenic fractional distillation columns interlinked with two equilibrators for separating a DT and hydrogen feed stream into four product streams, consisting of a stream of high purity D.sub.2, DT, T.sub.2, and a tritium-free stream of HD for waste disposal.

Bartlit, John R. (Los Alamos, NM); Denton, William H. (Abingdon, GB3); Sherman, Robert H. (Los Alamos, NM)

1982-01-01T23:59:59.000Z

26

Hydrogen isotope separation from water  

DOE Patents (OSTI)

A process for separating tritium from tritium-containing water or deuterium enrichment from water is described. The process involves selective, laser-induced two-photon excitation and photodissociation of those water molecules containing deuterium or tritium followed by immediate reaction of the photodissociation products with a scavenger gas which does not substantially absorb the laser light. The reaction products are then separated from the undissociated water. (auth)

Jensen, R.J.

1975-09-01T23:59:59.000Z

27

ISOTOPE SEPARATION AND ISOTOPE EXCHANGE. A Bibliography with Abstracts  

SciTech Connect

The unclassified literature covering 2498 reports from 1907 through 1957 has been searched for isotopic exchange and isotepic separation reactions involving U and the lighter elements of the periodic chart through atomic number 30. From 1953 to 1957, all elements were included Numerous references to isotope properties, isotopic ratios, and kinetic isotope effects were included. This is a complete revision of TID-3036 (Revised) issued June 4, 1954. An author index is included. (auth)

Begun, G.M.

1959-10-28T23:59:59.000Z

28

Electromagnetic Isotope Separation Lab (EMIS) | ORNL  

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

Electromagnetic Isotope Separation Lab Electromagnetic Isotope Separation Lab May 30, 2013 ORNL established the Stable Isotope Enrichment Laboratory (SIEL) as part of a project funded by the DOE Office of Science, Nuclear Physics Program to develop a modernized electromagnetic isotope separator (EMIS), optimized for separation of a wide range of stable isotopes. The SIEL is located in the Building 6010 Shield Test Station, space formerly allocated to the Oak Ridge Electron Linear Accelerator, on the main campus of ORNL. ORNL staff have designed and built a nominal 10 mA ion current EMIS (sum of all isotopes at the collector) in the SIEL. This EMIS is currently being tested to determine basic performance metrics such as throughput and enrichment factor per pass. This EMIS unit and space will be used to

29

Laser Isotope Enrichment for Medical and Industrial Applications  

SciTech Connect

Laser Isotope Enrichment for Medical and Industrial Applications by Jeff Eerkens (University of Missouri), Jay Kunze (Idaho State University), and Leonard Bond (Idaho National Laboratory) The principal isotope enrichment business in the world is the enrichment of uranium for commercial power reactor fuels. However, there are a number of other needs for separated isotopes. Some examples are: 1) Pure isotopic targets for irradiation to produce medical radioisotopes. 2) Pure isotopes for semiconductors. 3) Low neutron capture isotopes for various uses in nuclear reactors. 4) Isotopes for industrial tracer/identification applications. Examples of interest to medicine are targets to produce radio-isotopes such as S-33, Mo-98, Mo-100, W-186, Sn-112; while for MRI diagnostics, the non-radioactive Xe-129 isotope is wanted. For super-semiconductor applications some desired industrial isotopes are Si-28, Ga-69, Ge-74, Se-80, Te-128, etc. An example of a low cross section isotope for use in reactors is Zn-68 as a corrosion inhibitor material in nuclear reactor primary systems. Neutron activation of Ar isotopes is of interest in industrial tracer and diagnostic applications (e.g. oil-logging). . In the past few years there has been a sufficient supply of isotopes in common demand, because of huge Russian stockpiles produced with old electromagnetic and centrifuge separators previously used for uranium enrichment. Production of specialized isotopes in the USA has been largely accomplished using old ”calutrons” (electromagnetic separators) at Oak Ridge National Laboratory. These methods of separating isotopes are rather energy inefficient. Use of lasers for isotope separation has been considered for many decades. None of the proposed methods have attained sufficient proof of principal status to be economically attractive to pursue commercially. Some of the authors have succeeded in separating sulfur isotopes using a rather new and different method, known as condensation repression. In this scheme a gas, of the selected isotopes for enrichment, is irradiated with a laser at a particular wavelength that would excite only one of the isotopes. The entire gas is subject to low temperatures sufficient to cause condensation on a cold surface. Those molecules in the gas that the laser excited are not as likely to condense as are the unexcited molecules. Hence the gas drawn out of the system will be enriched in the isotope that was excited by the laser. We have evaluated the relative energy required in this process if applied on a commercial scale. We estimate the energy required for laser isotope enrichment is about 20% of that required in centrifuge separations, and 2% of that required by use of "calutrons".

Leonard Bond

2006-07-01T23:59:59.000Z

30

Process for producing enriched uranium having a {sup 235}U content of at least 4 wt. % via combination of a gaseous diffusion process and an atomic vapor laser isotope separation process to eliminate uranium hexafluoride tails storage  

DOE Patents (OSTI)

An uranium enrichment process capable of producing an enriched uranium, having a {sup 235}U content greater than about 4 wt. %, is disclosed which will consume less energy and produce metallic uranium tails having a lower {sup 235}U content than the tails normally produced in a gaseous diffusion separation process and, therefore, eliminate UF{sub 6} tails storage and sharply reduce fluorine use. The uranium enrichment process comprises feeding metallic uranium into an atomic vapor laser isotope separation process to produce an enriched metallic uranium isotopic mixture having a {sup 235} U content of at least about 2 wt. % and a metallic uranium residue containing from about 0.1 wt. % to about 0.2 wt. % {sup 235} U; fluorinating this enriched metallic uranium isotopic mixture to form UF{sub 6}; processing the resultant isotopic mixture of UF{sub 6} in a gaseous diffusion process to produce a final enriched uranium product having a {sup 235}U content of at least 4 wt. %, and up to 93.5 wt. % or higher, of the total uranium content of the product, and a low {sup 235}U content UF{sub 6} having a {sup 235}U content of about 0.71 wt. % of the total uranium content of the low {sup 235}U content UF{sub 6}; and converting this low {sup 235}U content UF{sub 6} to metallic uranium for recycle to the atomic vapor laser isotope separation process. 4 figs.

Horton, J.A.; Hayden, H.W. Jr.

1995-05-30T23:59:59.000Z

31

Process for producing enriched uranium having a .sup.235 U content of at least 4 wt. % via combination of a gaseous diffusion process and an atomic vapor laser isotope separation process to eliminate uranium hexafluoride tails storage  

DOE Patents (OSTI)

An uranium enrichment process capable of producing an enriched uranium, having a .sup.235 U content greater than about 4 wt. %, is disclosed which will consume less energy and produce metallic uranium tails having a lower .sup.235 U content than the tails normally produced in a gaseous diffusion separation process and, therefore, eliminate UF.sub.6 tails storage and sharply reduce fluorine use. The uranium enrichment process comprises feeding metallic uranium into an atomic vapor laser isotope separation process to produce an enriched metallic uranium isotopic mixture having a .sup.235 U content of at least about 2 wt. % and a metallic uranium residue containing from about 0.1 wt. % to about 0.2 wt. % .sup.235 U; fluorinating this enriched metallic uranium isotopic mixture to form UF.sub.6 ; processing the resultant isotopic mixture of UF.sub.6 in a gaseous diffusion process to produce a final enriched uranium product having a .sup.235 U content of at least 4 wt. %, and up to 93.5 wt. % or higher, of the total uranium content of the product, and a low .sup.235 U content UF.sub.6 having a .sup.235 U content of about 0.71 wt. % of the total uranium content of the low .sup.235 U content UF.sub.6 ; and converting this low .sup.235 U content UF.sub.6 to metallic uranium for recycle to the atomic vapor laser isotope separation process.

Horton, James A. (Livermore, CA); Hayden, Jr., Howard W. (Oakridge, TN)

1995-01-01T23:59:59.000Z

32

Isotope separation by photoselective dissociative electron capture  

DOE Patents (OSTI)

Disclosed is a method of separating isotopes based on photoselective electron capture dissociation of molecules having an electron capture cross section dependence on the vibrational state of the molecule. A molecular isotope source material is irradiated to selectively excite those molecules containing a desired isotope to a predetermined vibrational state having associated therewith an electron capture energy region substantially non-overlapping with the electron capture energy ranges associated with the lowest vibration states of the molecules. The isotope source is also subjected to electrons having an energy corresponding to the non-overlapping electron capture region whereby the selectively excited molecules preferentially capture electrons and dissociate into negative ions and neutrals. The desired isotope may be in the negative ion product or in the neutral product depending upon the mechanism of dissociation of the particular isotope source used. The dissociation product enriched in the desired isotope is then separated from the reaction system by conventional means. Specifically, [sup 235]UF[sub 6] is separated from a UF[sub 6] mixture by selective excitation followed by dissociative electron capture into [sup 235]UF[sub 5]- and F. 2 figs.

Stevens, C.G.

1978-08-29T23:59:59.000Z

33

Isotope separation by photoselective dissociative electron capture  

DOE Patents (OSTI)

A method of separating isotopes based on photoselective electron capture dissociation of molecules having an electron capture cross section dependence on the vibrational state of the molecule. A molecular isotope source material is irradiated to selectively excite those molecules containing a desired isotope to a predetermined vibrational state having associated therewith an electron capture energy region substantially non-overlapping with the electron capture energy ranges associated with the lowest vibration states of the molecules. The isotope source is also subjected to electrons having an energy corresponding to the non-overlapping electron capture region whereby the selectively excited molecules preferentially capture electrons and dissociate into negative ions and neutrals. The desired isotope may be in the negative ion product or in the neutral product depending upon the mechanism of dissociation of the particular isotope source used. The dissociation product enriched in the desired isotope is then separated from the reaction system by conventional means. Specifically, .sup.235 UF.sub.6 is separated from a UF.sub.6 mixture by selective excitation followed by dissociative electron capture into .sup.235 UF.sub.5 - and F.

Stevens, Charles G. (Pleasanton, CA)

1978-01-01T23:59:59.000Z

34

Tritium Isotope Separation Using Adsorption-Distillation Column  

Science Conference Proceedings (OSTI)

Technical Paper / Tritium Science and Technology - Tritium Science and Technology - Detritiation, Purification, and Isotope Separation

Satoshi Fukada

35

METHOD OF SEPARATING HYDROGEN ISOTOPES  

DOE Patents (OSTI)

The process of separating a gaseous mixture of hydrogen and tritium by contacting finely dlvided palladium with the mixture in order to adsorb the gases, then gradually heating the palladium and collecting the evolved fractlons, is described. The fraction first given off is richer in trltium than later fractions.

Salmon, O.N.

1958-12-01T23:59:59.000Z

36

Environmental site description for a Uranium Atomic Vapor Laser Isotope Separation (U-AVLIS) production plant at the Oak Ridge Gaseous Diffusion Plant Site  

Science Conference Proceedings (OSTI)

In January 1990, the Secretary of Energy approved a plan for the demonstration and deployment of the Uranium Atomic Vapor Laser Isotope Separation (U-AVLIS) technology, with the near-term goal to provide the necessary information to make a deployment decision by November 1992. The U-AVLIS process is based on electrostatic extraction of photoionized U-235 atoms from an atomic vapor stream created by electron-beam vaporization of uranium metal alloy. A programmatic document for use in screening DOE sites to locate the U-AVLIS production plant was developed and implemented in two parts (Wolsko et al. 1991). The first part consisted of a series of screening analyses, based on exclusionary and other criteria, that identified a reasonable number of candidate sites. These sites were then subjected to a more rigorous and detailed comparative analysis for the purpose of developing a short list of reasonable alternative sites for later environmental examination. This environmental site description (ESD) provides a detailed description of the ORGDP site and vicinity suitable for use in an environmental impact statement (EIS). The report is based on existing literature, data collected at the site, and information collected by Argonne National Laboratory (ANL) staff during a site visit. The organization of the ESD is as follows. Topics addressed in Sec. 2 include a general site description and the disciplines of geology, water resources, biotic resources, air resources, noise, cultural resources, land use, socioeconomics, and waste management. Identification of any additional data that would be required for an EIS is presented in Sec. 3. Following the site description and additional data requirements, Sec. 4 provides a short, qualitative assessment of potential environmental issues. 37 refs., 20 figs., 18 tabs.

Not Available

1991-09-01T23:59:59.000Z

37

Apparatus for separating and recovering hydrogen isotopes  

DOE Patents (OSTI)

An apparatus for recovering hydrogen and separating its isotopes. The apparatus includes a housing bearing at least a fluid inlet and a fluid outlet. A baffle is disposed within the housing, attached thereto by a bracket. A hollow conduit is coiled about the baffle, in spaced relation to the baffle and the housing. The coiled conduit is at least partially filled with a hydride. The hydride can be heated to a high temperature and cooled to a low temperature quickly by circulating a heat transfer fluid in the housing. The spacing between the baffle and the housing maximizes the heat exchange rate between the fluid in the housing and the hydride in the conduit. The apparatus can be used to recover hydrogen isotopes (protium, deuterium and tritium) from gaseous mixtures, or to separate hydrogen isotopes from each other.

Heung, Leung K. (Aiken, SC)

1994-01-01T23:59:59.000Z

38

Hydrogen isotope separation utilizing bulk getters  

DOE Patents (OSTI)

Tritium and deuterium are separated from a gaseous mixture thereof, derived from a nuclear fusion reactor or some other source, by providing a casing with a bulk getter therein for absorbing the gaseous mixture to produce an initial loading of the getter, partially desorbing the getter to produce a desorbed mixture which is tritium-enriched, pumping the desorbed mixture into a separate container, the remaining gaseous loading in the getter being deuterium-enriched, desorbing the getter to a substantially greater extent to produce a deuterium-enriched gaseous mixture, and removing the deuterium-enriched mixture into another container. The bulk getter may comprise a zirconium-aluminum alloy, or a zirconium-vanadium-iron alloy. The partial desorption may reduce the loading by approximately fifty percent. The basic procedure may be extended to produce a multistage isotope separator, including at least one additional bulk getter into which the tritium-enriched mixture is absorbed. The second getter is then partially desorbed to produce a desorbed mixture which is further tritium-enriched. The last-mentioned mixture is then removed from the container for the second getter, which is then desorbed to a substantially greater extent to produce a desorbed mixture which is deuterium-enriched. The last-mentioned mixture is then removed so that the cycle can be continued and repeated. The method of isotope separation is also applicable to other hydrogen isotopes, in that the method can be employed for separating either deuterium or tritium from normal hydrogen.

Knize, Randall J. (Los Angeles, CA); Cecchi, Joseph L. (Lawrenceville, NJ)

1991-01-01T23:59:59.000Z

39

Hydrogen isotope separation utilizing bulk getters  

DOE Patents (OSTI)

Tritium and deuterium are separated from a gaseous mixture thereof, derived from a nuclear fusion reactor or some other source, by providing a casing with a bulk getter therein for absorbing the gaseous mixture to produce an initial loading of the getter, partially desorbing the getter to produce a desorbed mixture which is tritium-enriched, pumping the desorbed mixture into a separate container, the remaining gaseous loading in the getter being deuterium-enriched, desorbing the getter to a substantially greater extent to produce a deuterium-enriched gaseous mixture, and removing the deuterium-enriched mixture into another container. The bulk getter may comprise a zirconium-aluminum alloy, or a zirconium-vanadium-iron alloy. The partial desorption may reduce the loading by approximately fifty percent. The basic procedure may be extended to produce a multistage isotope separator, including at least one additional bulk getter into which the tritium-enriched mixture is absorbed. The second getter is then partially desorbed to produce a desorbed mixture which is further tritium-enriched. The last-mentioned mixture is then removed from the container for the second getter, which is then desorbed to a substantially greater extent to produce a desorbed mixture which is deuterium-enriched. The last-mentioned mixture is then removed so that the cycle can be continued and repeated. The method of isotope separation is also applicable to other hydrogen isotopes, in that the method can be employed for separating either deuterium or tritium from normal hydrogen.

Knize, Randall J. (Los Angeles, CA); Cecchi, Joseph L. (Lawrenceville, NJ)

1990-01-01T23:59:59.000Z

40

Hydrogen isotope separation utilizing bulk getters  

DOE Patents (OSTI)

Tritium and deuterium are separated from a gaseous mixture thereof, derived from a nuclear fusion reactor or some other source, by providing a casing with a bulk getter therein for absorbing the gaseous mixture to produce an initial loading of the getter, partially desorbing the getter to produce a desorbed mixture which is tritium-enriched, pumping the desorbed mixture into a separate container, the remaining gaseous loading in the getter being deuterium-enriched, desorbing the getter to a substantially greater extent to produce a deuterium-enriched gaseous mixture, and removing the deuterium-enriched mixture into another container. The bulk getter may comprise a zirconium-aluminum alloy, or a zirconium-vanadium-iron alloy. The partial desorption may reduce the loading by approximately fifty percent. The basic procedure may be extended to produce a multistage isotope separator, including at least one additional bulk getter into which the tritium-enriched mixture is absorbed. The second getter is then partially desorbed to produce a desorbed mixture which is further tritium-enriched. The last-mentioned mixture is then removed from the container for the second getter, which is then desorbed to a substantially greater extent to produce a desorbed mixture which is deuterium-enriched. The last-mentioned mixture is then removed so that the cycle can be continued and repeated. The method of isotope separation is also applicable to other hydrogen isotopes, in that the method can be employed for separating either deuterium or tritium from normal hydrogen. 4 figures.

Knize, R.J.; Cecchi, J.L.

1991-08-20T23:59:59.000Z

Note: This page contains sample records for the topic "laser isotope separation" 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

Environmental site description for a Uranium Atomic Vapor Laser Isotope Separation (U-AVLIS) production plant at the Paducah Gaseous Diffusion Plant site  

Science Conference Proceedings (OSTI)

Uranium enrichment in the United States has utilized a diffusion process to preferentially enrich the U-235 isotope in the uranium product. The U-AVLIS process is based on electrostatic extraction of photoionized U-235 atoms from an atomic vapor stream created by electron-beam vaporization of uranium metal alloy. The U-235 atoms are ionized when precisely tuned laser light -- of appropriate power, spectral, and temporal characteristics -- illuminates the uranium vapor and selectively photoionizes the U-235 isotope. A programmatic document for use in screening DOE site to locate a U-AVLIS production plant was developed and implemented in two parts. The first part consisted of a series of screening analyses, based on exclusionary and other criteria, that identified a reasonable number of candidate sites. These sites were subjected to a more rigorous and detailed comparative analysis for the purpose of developing a short list of reasonable alternative sites for later environmental examination. This environmental site description (ESD) provides a detailed description of the PGDP site and vicinity suitable for use in an environmental impact statement (EIS). The report is based on existing literature, data collected at the site, and information collected by Argonne National Laboratory (ANL) staff during a site visit. 65 refs., 15 tabs.

Marmer, G.J.; Dunn, C.P.; Moeller, K.L.; Pfingston, J.M.; Policastro, A.J.; Yuen, C.R.; Cleland, J.H. (ed.)

1991-09-01T23:59:59.000Z

42

CONTROL SYSTEM FOR ISOTOPE SEPARATING APPARATUS  

DOE Patents (OSTI)

A method is described for controlling the position of the ion beams in a calutron used for isotope separation. The U/sup 238/ beams is centered over the U/sup 235/ receiving pocket, the operator monitoring the beam until a maximum reading is achieved on the meter connected to that pocket. Then both beams are simultaneously shifted by a preselected amount to move the U/sup 235/ beam over the U/sup 235/ pocket. A slotted door is placed over the entrance to that pocket during the U/sup 238/ beam centering to reduce the contamination to the pocket, while allowing enough beam to pass for monitoring purposes.

Barnes, S.W.

1960-01-26T23:59:59.000Z

43

Novel hybrid isotope separation scheme and apparatus  

DOE Patents (OSTI)

A method of yielding selectively a desired enrichment in a specific isotope including the steps of inputting into a spinning chamber a gas from which the specific isotope is to be isolated, radiating the gas with frequencies characteristic of the absorption of a particular isotope of the atomic or molecular gas, thereby inducing a photoionization reaction of the desired isotope, and collecting the specific isotope ion by suitable ion collection means.

Maya, Jakob (Brookline, MA)

1991-01-01T23:59:59.000Z

44

Mantle Helium And Carbon Isotopes In Separation Creek Geothermal...  

Open Energy Info (EERE)

Mantle Helium And Carbon Isotopes In Separation Creek Geothermal Springs, Three Sisters Area, Central Oregon- Evidence For Renewed Volcanic Activity Or A Long Term Steady State...

45

Mantle Helium And Carbon Isotopes In Separation Creek Geothermal Springs,  

Open Energy Info (EERE)

Mantle Helium And Carbon Isotopes In Separation Creek Geothermal Springs, Mantle Helium And Carbon Isotopes In Separation Creek Geothermal Springs, Three Sisters Area, Central Oregon- Evidence For Renewed Volcanic Activity Or A Long Term Steady State System(Question) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Conference Paper: Mantle Helium And Carbon Isotopes In Separation Creek Geothermal Springs, Three Sisters Area, Central Oregon- Evidence For Renewed Volcanic Activity Or A Long Term Steady State System(Question) Details Activities (1) Areas (1) Regions (0) Abstract: Here we present the helium and carbon isotope results from the initial study of a fluid chemistry-monitoring program started in the summer of 2001 near the South Sister volcano in central Oregon. The Separation Creek area which is several miles due west of the volcano is the locus of

46

VELOCITY SELECTOR METHOD FOR THE SEPARATION OF ISOTOPES  

DOE Patents (OSTI)

A velocity selector apparatus is described for separating and collecting an enriched fraction of the isotope of a particular element. The invention has the advantage over conventional mass spectrometers in that a magnetic field is not used, doing away with the attendant problems of magnetic field variation. The apparatus separates the isotopes by selectively accelerating the ionized constituents present in a beam of the polyisotopic substance that are of uniform kinetic energy, the acceleration being applied intermittently and at spaced points along the beam and in a direction normal to the direction of the propagation of the uniform energy beam whereby a transverse displacement of the isotopic constituents of different mass is obtained.

Britten, R.J.

1957-12-31T23:59:59.000Z

47

Metal hydride based isotope separation: Large-scale operations  

DOE Green Energy (OSTI)

A program to develop a metal hydride based hydrogen isotope separation process began at the Savannah River Laboratory in 1980. This semi-continuous gas chromatographic separation process will be used in new tritium facilities at the Savannah River Site. A tritium production unit is scheduled to start operation in 1993. An experimental, large-scale unit is currently being tested using protium and deuterium. Operation of the large-scale unit has demonstrated separation of mixed hydrogen isotopes (55% protium and 45% deuterium), resulting in protium and deuterium product streams with purities better than 99.5%. 3 refs., 4 figs.

Horen, A.S.; Lee, Myung W.

1991-01-01T23:59:59.000Z

48

Metal hydride based isotope separation: Large-scale operations  

DOE Green Energy (OSTI)

A program to develop a metal hydride based hydrogen isotope separation process began at the Savannah River Laboratory in 1980. This semi-continuous gas chromatographic separation process will be used in new tritium facilities at the Savannah River Site. A tritium production unit is scheduled to start operation in 1993. An experimental, large-scale unit is currently being tested using protium and deuterium. Operation of the large-scale unit has demonstrated separation of mixed hydrogen isotopes (55% protium and 45% deuterium), resulting in protium and deuterium product streams with purities better than 99.5%. 3 refs., 4 figs.

Horen, A.S.; Lee, Myung W.

1991-12-31T23:59:59.000Z

49

New Contact Device for Separation of Hydrogen Isotopes in the Water-Hydrogen System  

Science Conference Proceedings (OSTI)

Technical Paper / Tritium Science and Technology - Tritium Science and Technology - Detritiation, Purification, and Isotope Separation

I. L. Rastunova; M. B. Rozenkevich

50

Separation of Hydrogen Isotopes by Thermal Diffusion  

SciTech Connect

At high hot wall temperatures the gas phase thermal diffusion column acts as an atomic rather than a molecular separator. A modified theory was developed to describe the process. Equivalent transport equations were derived for the two nuclides in a binary atomic mixture. The equations are identical in form to those normally encountered in thermal diffusion column theory. Experiments to test the theory were carried out with two 3-meter columns. Experimental results with deuterium-tritium mixtures were found to be in satisfactory agreement with theory, and it was concluded that the theory was sufficiently accurate for design purposes.

Rutherford, W. M.; Lindsay, C. N.

1985-09-01T23:59:59.000Z

51

Optically pumped isotopic ammonia laser system  

DOE Patents (OSTI)

An optically pumped isotopic ammonia laser system which is capable of producing a plurality of frequencies in the middle infrared spectral region. Two optical pumping mechanisms are disclosed, i.e., pumping on R(J) and lasing on P(J) in response to enhancement of rotational cascade lasing including stimulated Raman effects, and, pumping on R(J) and lasing on P(J+2). The disclosed apparatus for optical pumping include a hole coupled cavity and a grating coupled cavity.

Buchwald, Melvin I. (Santa Fe, NM); Jones, Claude R. (Los Alamos, NM); Nelson, Leonard Y. (Seattle, WA)

1982-01-01T23:59:59.000Z

52

RECTIFIED ABSORPTION METHOD FOR THE SEPARATION OF HYDROGEN ISOTOPES  

DOE Patents (OSTI)

A method is described for separating and recovering heavy hydrogen isotopes from gaseous mixtures by multiple stage cyclic absorption and rectification from an approximate solvent. In particular, it is useful for recovering such isoteoes from ammonia feedstock streams containing nitrogen solvent. Modifications of the process ranging from isobaric to isothermal are provided. Certain impurities are tolerated, giving advantages over conventional fractional distillation processes. (AEC)

Hunt, C.D.; Hanson, D.N.

1961-10-17T23:59:59.000Z

53

Hydrogen Isotope Separation System for the Tokamak Experimental Power Reactor  

SciTech Connect

An isotopic separation system for processing the fuel in the Tokamak Experimental Power Reactor is described. Two cryogenic distillation columns are used in sequence to recover 80% of the hydrogen from a fuel mixture originally containing equal parts of deuterium and tritium with a 1% hydrogen impurity. The hydrogen thus removed contains less than 1/2% tritium, which may be recovered in a separate system designed for that purpose. It is assumed that separation of the deuterium and the tritium is not required. A total tritium inventory of approximately 38,000 Ci (3.8 g) is projected.

Wilkes, W. R.

1976-03-01T23:59:59.000Z

54

NOVEL CONCEPTS FOR ISOTOPIC SEPARATION OF 3HE/4HE  

SciTech Connect

The research outlined below established theoretical proof-of-concept using ab initio calculations that {sup 3}He can be separated from {sup 4}He by taking advantage of weak van der Waals interactions with other higher molecular weight rare gases such as xenon. To the best of our knowledge, this is the only suggested method that exploits the physical differences of the isotopes using a chemical interaction.

Roy, L.; Nigg, H.; Watson, H.

2012-09-04T23:59:59.000Z

55

Investigation of Separation Performances of Various Isotope Exchange Catalysts for the Deuterium-Hydrogen System  

Science Conference Proceedings (OSTI)

Isotope Separation / Proceedings of the Sixth International Conference on Tritium Science and Technology Tsukuba, Japan November 12-16, 2001

I. Cristescu; Ioana-R. Cristescu; U. Tamm; R.-D. Penzhorn; C. J. Caldwell-Nichols

56

ISOTOPES  

E-Print Network (OSTI)

Theory of Isotope Separation as Applied to the Large~scale Production of 235 u National Nuclear Energy

Lederer, C. Michael

2013-01-01T23:59:59.000Z

57

Isotopic Analysis At Separation Creek Area (Van Soest, Et Al., 2002) | Open  

Open Energy Info (EERE)

Isotopic Analysis At Separation Creek Area (Van Soest, Et Al., 2002) Isotopic Analysis At Separation Creek Area (Van Soest, Et Al., 2002) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Isotopic Analysis- Fluid At Separation Creek Area (Van Soest, Et Al., 2002) Exploration Activity Details Location Separation Creek Area Exploration Technique Isotopic Analysis- Fluid Activity Date Usefulness useful DOE-funding Unknown References M. C. van Soest, B. M. Kennedy, W. C. Evans, R. H. Mariner (2002) Mantle Helium And Carbon Isotopes In Separation Creek Geothermal Springs, Three Sisters Area, Central Oregon- Evidence For Renewed Volcanic Activity Or A Long Term Steady State System(Question) Retrieved from "http://en.openei.org/w/index.php?title=Isotopic_Analysis_At_Separation_Creek_Area_(Van_Soest,_Et_Al.,_2002)&oldid=687475"

58

Tritium Isotope Separation Using Adsorption-Distillation Column  

Science Conference Proceedings (OSTI)

In order to miniaturize the height of a distillation tower for the detritiation of waste water from fusion reactors, two experiments were conducted: (1) liquid frontal chromatography of tritium water eluting through an adsorption column and (2) water distillation using a column packed with adsorbent particles. The height of the distillation tower depends on the height equivalent to a theoretical plate, HETP, and the equilibrium isotope separation factor, {alpha}{sub H-T}{sup equi}. The adsorption action improved not only HETP but also {alpha}{sub H-T}{sup equi}. Since the adsorption-distillation method proposed here can shorten the tower height with keeping advantages of the distillation, it may bring an excellent way for miniaturizing the distillation tower to detritiate a large amount of waste water from fusion reactors.

Fukada, Satoshi [Kyushu University (Japan)

2005-07-15T23:59:59.000Z

59

Isotope separation by selective charge conversion and field deflection  

DOE Patents (OSTI)

A deuterium-tritium separation system wherein a source beam comprised of positively ionized deuterium (D.sup.+) and tritium (T.sup.+) is converted at different charge-exchange cell sections of the system to negatively ionized deuterium (D.sup.-) and tritium (T.sup.-). First, energy is added to the beam to accelerate the D.sup.+ ions to the velocity that is optimum for conversion of the D.sup.+ ions to D.sup.- ions in a charge-exchange cell. The T.sup.+ ions are accelerated at the same time, but not to the optimum velocity since they are heavier than the D.sup.+ ions. The T.sup.+ ions are, therefore, not converted to T.sup.- ions when the D.sup.+ ions are converted to D.sup.- ions. This enables effective separation of the beam by deflection of the isotopes with an electrostatic field, the D.sup.- ions being deflected in one direction and the T.sup.+ ions being deflected in the opposite direction. Next, more energy is added to the deflected beam of T.sup.+ ions to bring the T.sup.+ ions to the optimum velocity for their conversion to T.sup.- ions. In a particular use of the invention, the beams of D.sup.- and T.sup.- ions are separately further accelerated and then converted to energetic neutral particles for injection as fuel into a thermonuclear reactor. The reactor exhaust of D.sup.+ and T.sup.+ and the D.sup.+ and T.sup.+ that was not converted in the respective sections is combined with the source beam and recycled through the system to increase the efficiency of the system.

Hickman, Robert G. (Livermore, CA)

1978-01-01T23:59:59.000Z

60

Liquid-phase thermal diffusion isotope separation apparatus and method having tapered column  

DOE Patents (OSTI)

A thermal diffusion counterflow method and apparatus for separating isotopes in solution in which the solution is confined in a long, narrow, vertical slit which tapers from bottom to top. The variation in the width of the slit permits maintenance of a stable concentration distribution with relatively long columns, thus permitting isotopic separation superior to that obtained in the prior art.

Rutherford, W.M.

1985-12-04T23:59:59.000Z

Note: This page contains sample records for the topic "laser isotope separation" 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

Gas Chromatographic Separation of Hydrogen Isotopes on Molecular Sieves  

Science Conference Proceedings (OSTI)

Tritium Processing / Proceedings of the Third Topical Meeting on Tritium Technology in Fission, Fusion and Isotopic Applications (Toronto, Ontario, Canada, May 1-6, 1988)

R. Vogd; H. Ringel; H. Hackfort; T. Schober; C. Dieker

62

Analysis of gas centrifuge cascade for separation of multicomponent isotopes and optimal feed position  

SciTech Connect

Analysis of the concentration distribution in a gas centrifuge cascade for separation of multicomponent isotope mixtures is different from that in a cascade for separation of two-component mixtures. This paper presents the governing equations for a multicomponent isotope separation cascade. Numerically predicted separation factors for the gas centrifuge cascade agree well with the experimental data. A theoretical optimal feed position is derived for a short square cascade for a two-component mixture in a close-separation case. The optimal feed position for a gas centrifuge cascade for separation of multicomponent mixture is discussed.

Chuntong Ying; Hongjiang Wu; Mingsheng Zhou; Yuguang Nie; Guangjun Liu [Tsinghua Univ., Beijing (China)

1997-10-01T23:59:59.000Z

63

Critical review of progress report on reactive matrix isotope separation by E. Catalano, E. Lee, and M. Schwab  

SciTech Connect

This paper provides an evaluation and critical review of the possibilities for uranium isotope separation using matrix techniques.

Catalano, E.

1975-08-19T23:59:59.000Z

64

The laser ion source trap for highest isobaric selectivity in online exotic isotope production  

Science Conference Proceedings (OSTI)

The improvement in the performance of a conventional laser ion source in the laser ion source and trap (LIST) project is presented, which envisages installation of a repeller electrode and a linear Paul trap/ion guide structure. This approach promises highest isobaric purity and optimum temporal and spatial control of the radioactive ion beam produced at an online isotope separator facility. The functionality of the LIST was explored at the offline test separators of University of Mainz (UMz) and ISOLDE/CERN, using the UMz solid state laser system. Ionization efficiency and selectivity as well as time structure and transversal emittance of the produced ion beam was determined. Next step after complete characterization is the construction and installation of the radiation-hard final trap structure and its first online application.

Schwellnus, F.; Gottwald, T.; Mattolat, C.; Wendt, K. [Institut fuer Physik, Johannes Gutenberg-Universitaet, D-55099 Mainz (Germany); Blaum, K. [Max-Planck-Institut fuer Kernphysik, Saupfercheckweg 1, D-69117 Heidelberg (Germany); Catherall, R.; Crepieux, B.; Fedosseev, V.; Marsh, B.; Rothe, S.; Stora, T. [CERN, CH-1211 Geneva 23 (Switzerland); Kluge, H.-J. [GSI, Planckstrasse 1, D-64291 Darmstadt (Germany)

2010-02-15T23:59:59.000Z

65

Quantifying Uranium Isotope Ratios Using Resonance Ionization Mass Spectrometry: The Influence of Laser Parameters on Relative Ionization Probability  

Science Conference Proceedings (OSTI)

Resonance Ionization Mass Spectrometry (RIMS) has been developed as a method to measure relative uranium isotope abundances. In this approach, RIMS is used as an element-selective ionization process to provide a distinction between uranium atoms and potential isobars without the aid of chemical purification and separation. We explore the laser parameters critical to the ionization process and their effects on the measured isotope ratio. Specifically, the use of broad bandwidth lasers with automated feedback control of wavelength was applied to the measurement of {sup 235}U/{sup 238}U ratios to decrease laser-induced isotopic fractionation. By broadening the bandwidth of the first laser in a 3-color, 3-photon ionization process from a bandwidth of 1.8 GHz to about 10 GHz, the variation in sequential relative isotope abundance measurements decreased from >10% to less than 0.5%. This procedure was demonstrated for the direct interrogation of uranium oxide targets with essentially no sample preparation. A rate equation model for predicting the relative ionization probability has been developed to study the effect of variation in laser parameters on the measured isotope ratio. This work demonstrates that RIMS can be used for the robust measurement of uranium isotope ratios.

Isselhardt, B H

2011-09-06T23:59:59.000Z

66

Isotopic Effect on Ion Mobility and Separation of Isotopomers by High-Field Ion Mobility Spectrometry  

SciTech Connect

Since early 1900-s, when vacuum techniques and ion detectors first enabled investigations of gas-phase ions, two approaches to their separation and characterization have emerged - mass spectrometry (MS) and ion mobility spectrometry (IMS).1,2 Though both exploit that distinct charged species move in electric fields differently, MS is performed in vacuum and is based only on the ion mass/charge (m/q) ratio while IMS involves sufficiently dense buffer gases and relies on ion transport properties. The first major discovery enabled by MS was the existence of isotopes by Thomson and Aston,3 and isotopic analyses have since been integral to MS. In particular, the preparative separation of U isotopes using Lawrence’s Calutron was the first industrial application of MS,4 and isotopic labeling is key to MS quantification methods. With IMS, the issue of isotopes was largely ignored as the resolving power (R) was generally too low for their separation. Here, we demonstrate that recently developed high-resolution differential IMS can separate isotopic molecular ions, including nominal isobars with different isotopic content and isotopomers. This capability may enable a new method for isotope separation in a small-scale format at ambient pressure and aid localization of labeled sites in various molecules. Perhaps most importantly, the isotopic shifts depend on the labeled atom position and thus may contain the kind of detailed structural information that is available in solution or solid state using tools such as NMR but has not generally been obtainable for gas-phase ions.

Shvartsburg, Alexandre A.; Clemmer, David E.; Smith, Richard D.

2010-10-01T23:59:59.000Z

67

Nested reactor chamber and operation for Hg-196 isotope separation process  

DOE Patents (OSTI)

The present invention is directed to an apparatus for use in .sup.196 Hg separation and its method of operation. Specifically, the present invention is directed to a nested reactor chamber useful for .sup.196 Hg isotope separation reactions avoiding the photon starved condition commonly encountered in coaxial reactor systems.

Grossman, Mark W. (Belmont, MA)

1991-01-01T23:59:59.000Z

68

National uses and needs for separated stable isotopes in physics, chemistry, and geoscience research  

SciTech Connect

Present uses of separated stable isotopes in the fields of physics, chemistry, and the geosciences have been surveyed to identify current supply problems and to determine future needs. Demand for separated isotopes remains strong, with 220 different nuclides having been used in the past three years. The largest needs, in terms of both quantity and variety of isotopes, are found in nuclear physics research. Current problems include a lack of availability of many nuclides, unsatisfactory enrichment of rare species, and prohibitively high costs for certain important isotopes. It is expected that demands for separated isotopes will remain roughly at present levels, although there will be a shift toward more requests for highly enriched rare isotopes. Significantly greater use will be made of neutron-rich nuclides below A = 100 for producing exotic ion beams at various accelerators. Use of transition metal nuclei for nuclear magnetic resonance spectroscopy will expand. In addition, calibration standards will be required for the newer techniques of radiological dating, such as the Sm/Nd and Lu/Hf methods, but in relatively small quantities. Most members of the research community would be willing to pay considerably more than they do now to maintain adequate supplies of stable isotopes.

Zisman, M.S.

1982-01-01T23:59:59.000Z

69

Isotope enrichment by frequency-tripled temperature tuned neodymium laser photolysis of formaldehyde  

DOE Patents (OSTI)

Enrichment of carbon, hydrogen and/or oxygen isotopes by means of isotopically selective photo-predissociation of formaldehyde is achieved by irradiation provided by a frequency-tripled, temperature tuned neodymium laser.

Marling, John B. (Livermore, CA)

1977-01-01T23:59:59.000Z

70

Isotope Enrichment Detection by Laser Ablation - Dual Tunable Diode Laser Absorption Spectrometry  

Science Conference Proceedings (OSTI)

The rapid global expansion of nuclear energy is motivating the expedited development of new safeguards technology to mitigate potential proliferation threats arising from monitoring gaps within the uranium enrichment process. Current onsite enrichment level monitoring methods are limited by poor sensitivity and accuracy performance. Offsite analysis has better performance, but this approach requires onsite hand sampling followed by time-consuming and costly post analysis. These limitations make it extremely difficult to implement comprehensive safeguards accounting measures that can effectively counter enrichment facility misuse. In addition, uranium enrichment by modern centrifugation leads to a significant proliferation threat, since the centrifuge cascades can quickly produce a significant quantity of highly enriched uranium (HEU). The Pacific Northwest National Laboratory is developing an engineered safeguards approach having continuous aerosol particulate collection and uranium isotope analysis to provide timely detection of HEU production in a low enriched uranium facility. This approach is based on laser vaporization of aerosol particulate samples, followed by wavelength tuned laser diode spectroscopy, to characterize the 235U/238U isotopic ratio by subtle differences in atomic absorption wavelengths arising from differences in each isotope’s nuclear mass, volume, and spin (hyperfine structure for 235U). Environmental sampling media is introduced into a small, reduced pressure chamber, where a focused pulsed laser vaporizes a 10 to 20-µm sample diameter. The ejected plasma forms a plume of atomic vapor. A plume for a sample containing uranium has atoms of the 235U and 238U isotopes present. Tunable diode lasers are directed through the plume to selectively excite each isotope and their presence is detected by monitoring absorbance signals on a shot-to-shot basis. Single-shot detection sensitivity approaching the femtogram range and abundance uncertainty less than 10% have been demonstrated with measurements on surrogate materials. In this paper we present measurement results on samples containing background materials (e.g., dust, minerals, soils) laced with micron-sized target particles having isotopic ratios ranging from 1 to 50%.

Anheier, Norman C.; Bushaw, Bruce A.

2009-07-01T23:59:59.000Z

71

Investigation related to hydrogen isotopes separation by cryogenic distillation  

Science Conference Proceedings (OSTI)

Research conducted in the last fifty years has shown that one of the most efficient techniques of removing tritium from the heavy water used as moderator and coolant in CANDU reactors (as that operated at Cernavoda (Romania)) is hydrogen cryogenic distillation. Designing and implementing the concept of cryogenic distillation columns require experiments to be conducted as well as computer simulations. Particularly, computer simulations are of great importance when designing and evaluating the performances of a column or a series of columns. Experimental data collected from laboratory work will be used as input for computer simulations run at larger scale (for The Pilot Plant for Tritium and Deuterium Separation) in order to increase the confidence in the simulated results. Studies carried out were focused on the following: - Quantitative analyses of important parameters such as the number of theoretical plates, inlet area, reflux flow, flow-rates extraction, working pressure, etc. - Columns connected in series in such a way to fulfil the separation requirements. Experiments were carried out on a laboratory-scale installation to investigate the performance of contact elements with continuous packing. The packing was manufactured in our institute. (authors)

Bornea, A.; Zamfirache, M.; Stefanescu, I.; Preda, A.; Balteanu, O.; Stefan, I. [INC-DTCI-ICSI Rm. Valcea, str.Uzinei, Nr.4, 240050 (Romania)

2008-07-15T23:59:59.000Z

72

Isotope separation by photodissociation of Van der Waal's molecules  

DOE Patents (OSTI)

A method of separating isotopes based on the dissociation of a Van der Waal's complex. A beam of molecules of a Van der Waal's complex containing, as one partner of the complex, a molecular species in which an element is present in a plurality of isotopes is subjected to radiation from a source tuned to a frequency which will selectively excite vibrational motion by a vibrational transition or through electronic transition of those complexed molecules of the molecular species which contain a desired isotope. Since the Van der Waal's binding energy is much smaller than the excitational energy of vibrational motion, the thus excited Van der Waal's complex dissociate into molecular components enriched in the desired isotope. The recoil velocity associated with vibrational to translational and rotational relaxation will send the separated molecules away from the beam whereupon the product enriched in the desired isotope can be separated from the constituents of the beam.

Lee, Yuan T. (Berkeley, CA)

1977-01-01T23:59:59.000Z

73

APPLICABILITY OF GAS CENTRIFUGE TO ISOTOPE SEPARATION FOR ELEMENTS HEAVIER THAN TITANIUM  

SciTech Connect

The applicability of the gas centrifuge to the separation of the isotopes of the elements from Ti through U was examined. The suitable elsments were determined, and their effects on required centrifuge characteristics were surveyed. The performance of cascades of various aires with different gages was explored, and the cost of a pilot plant program to develop basic separation data was estimated. (F.S.)

Barker, J.J.

1956-09-30T23:59:59.000Z

74

Influence of liquid structure on diffusive isotope separation in molten silicates and aqueous solutions  

Science Conference Proceedings (OSTI)

Molecular diffusion in natural volcanic liquids discriminates between isotopes of major ions (e.g., Fe, Mg, Ca, and Li). Although isotope separation by diffusion is expected on theoretical grounds, the dependence on mass is highly variable for different elements and in different media. Silicate liquid diffusion experiments using simple liquid compositions were carried out to further probe the compositional dependence of diffusive isotopic discrimination and its relationship to liquid structure. Two diffusion couples consisting of the mineral constituents anorthite (CaAl{sub 2}Si{sub 2}O{sub 8}; denoted AN), albite (NaAlSi{sub 3}O{sub 8}; denoted AB), and diopside (CaMgSi{sub 2}O{sub 6}; denoted DI) were held at 1450°C for 2 h and then quenched to ambient pressure and temperature. Major-element as well as Ca and Mg isotope profiles were measured on the recovered quenched glasses. In both experiments, Ca diffuses rapidly with respect to Si. In the AB–AN experiment, D{sub Ca}/D{sub Si} ~ 20 and the efficiency of isotope separation for Ca is much greater than in natural liquid experiments where D{sub Ca}/D{sub Si} ~ 1. In the AB–DI experiment, D{sub Ca}/D{sub Si} ~ 6 and the efficiency of isotope separation is between that of the natural liquid experiments and the AB–AN experiment. In the AB–DI experiment, D{sub Mg}/D{sub Si} ~ 1 and the efficiency of isotope separation for Mg is smaller than it is for Ca yet similar to that observed for Mg in natural liquids. The results from the experiments reported here, in combination with results from natural volcanic liquids, show clearly that the efficiency of diffusive separation of Ca isotopes is systematically related to the solvent-normalized diffusivity—the ratio of the diffusivity of the cation (D{sub Ca}) to the diffusivity of silicon (D{sub Si}). The results on Ca isotopes are consistent with available data on Fe, Li, and Mg isotopes in silicate liquids, when considered in terms of the parameter D{sub cation}/D{sub Si}. Cations diffusing in aqueous solutions display a similar relationship between isotopic separation efficiency and D{sub cation} =D{sub H 2 O} , although the efficiencies are smaller than in silicate liquids. Our empirical relationship provides a tool for predicting the magnitude of diffusive isotopic effects in many geologic environments and a basis for a more comprehensive theory of isotope separation in liquid solutions. We present a conceptual model for the relationship between diffusivity and liquid structure that is consistent with available data.

Watkins, J.M.; DePaolo, D.J.; Ryerson, F.J.; Peterson, B.

2011-03-01T23:59:59.000Z

75

A Low Temperature Distillation System for Separating Mixtures of Protium, Deuterium, and Tritium Isotopes  

SciTech Connect

A low temperature (24 K) distillation system for separating mixtures of hydrogen isotopes has been designed, fabricated, and delivered for use as the main component of the Hydrogen Isotope Separation System (HISS) at Mound. The HISS will handle feed mixtures of all six isotopic species of hydrogen (H2, HD, HT, D2, DT, T2) and will enrich the tritium while producing a stackable raffinate. Arther D. Little, Inc. (ADL) was the prime contractor for the distillation system. The design and fabrication techniques used for the HISS distillation system are similar to those used for previous stills which were also designed and built by ADL. The distillation system was tested with mixtures of protium and deuterium at the ADL shop. This system, as well as the feed, product, and raffinate handling systems are presently being installed at Mound where integrated testing is scheduled next calendar year.

Embury, Michael, C.; Watkins, Reed A.; Hinckley, Richard; Post, Jr., Arthur H.

1985-04-30T23:59:59.000Z

76

Isotopic Effect on Ion Mobility and Separation of Isotopomers by High-Field Ion Mobility  

E-Print Network (OSTI)

Isotopic Effect on Ion Mobility and Separation of Isotopomers by High-Field Ion Mobility ions, including isotopomers and isobars, using ion mobility spectrometry (IMS), specifically, the field about the ion geometry, potentially enabling a new approach to molecular structure characterization

Clemmer, David E.

77

L.C.C. laser isotope separation project progress report  

SciTech Connect

Progress is described in the following areas: matrix isolation of uranium hexafluoride in carbon monoxide host and obtainment of stable narrow bands in the 623cm{sup -1} region of uranium hexafluoride; and reactions of nitrogen oxide with uranium hexafluoride.

Catalano, E.

1974-12-02T23:59:59.000Z

78

Lithium Isotope Separation & Enrichment Technologies (4577), 2/9/2012  

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

Lithium Isotope Separation & Enrichment Technologies (4577) Lithium Isotope Separation & Enrichment Technologies (4577) Program or Field Office: Y-12 Site Office Location(s) (City/County/State): Oak Ridge, Anderson County, Tennessee Proposed Action Description: Submit by E-mail This is entirely a paper study. The scope of this Cooperative Research and Development (CRADA) is to: 1) systematically review existing potential lithium enrichment processes, 2) evaluate the individual process, 3) determine the economic feasibility, 4) rank the processes as a function of economic feasibility, technical probability, Health, Safety and Environmental impacts, 5) identify best candidate technology for proof of principle evaluation, 6) develop outside funding proposals, and 7) pursue funding to perform proof of principle/prototyping of candidate

79

Isotope Enrichment Detection by Laser Ablation - Laser Absorption Spectrometry: Automated Environmental Sampling and Laser-Based Analysis for HEU Detection  

SciTech Connect

The global expansion of nuclear power, and consequently the uranium enrichment industry, requires the development of new safeguards technology to mitigate proliferation risks. Current enrichment monitoring instruments exist that provide only yes/no detection of highly enriched uranium (HEU) production. More accurate accountancy measurements are typically restricted to gamma-ray and weight measurements taken in cylinder storage yards. Analysis of environmental and cylinder content samples have much higher effectiveness, but this approach requires onsite sampling, shipping, and time-consuming laboratory analysis and reporting. Given that large modern gaseous centrifuge enrichment plants (GCEPs) can quickly produce a significant quantity (SQ ) of HEU, these limitations in verification suggest the need for more timely detection of potential facility misuse. The Pacific Northwest National Laboratory (PNNL) is developing an unattended safeguards instrument concept, combining continuous aerosol particulate collection with uranium isotope assay, to provide timely analysis of enrichment levels within low enriched uranium facilities. This approach is based on laser vaporization of aerosol particulate samples, followed by wavelength tuned laser diode spectroscopy to characterize the uranium isotopic ratio through subtle differences in atomic absorption wavelengths. Environmental sampling (ES) media from an integrated aerosol collector is introduced into a small, reduced pressure chamber, where a focused pulsed laser vaporizes material from a 10 to 20-µm diameter spot of the surface of the sampling media. The plume of ejected material begins as high-temperature plasma that yields ions and atoms, as well as molecules and molecular ions. We concentrate on the plume of atomic vapor that remains after the plasma has expanded and then cooled by the surrounding cover gas. Tunable diode lasers are directed through this plume and each isotope is detected by monitoring absorbance signals on a shot-to-shot basis. The media is translated by a micron resolution scanning system, allowing the isotope analysis to cover the entire sample surface. We also report, to the best of our knowledge, the first demonstration of laser-based isotopic measurements on individual micron-sized particles that are minor target components in a much larger heterogeneous mix of ‘background’ particles. This composition is consistent with swipe and environmental aerosol samples typically collected for safeguards ES purposes. Single-shot detection sensitivity approaching the femtogram range and relative isotope abundance uncertainty better than 10% has been demonstrated using gadolinium isotopes as surrogate materials.

Anheier, Norman C.; Bushaw, Bruce A.

2010-01-01T23:59:59.000Z

80

Studies of hydrogen isotope separation using vanadium hydride in a temperature cycling process  

DOE Green Energy (OSTI)

Separations of gaseous HT-H/sub 2/ mixtures on vanadium monohydride were carried out using a two-column temperature cycling process similar to parametric pumping. An equilibrium theory of process operation is presented which was in qualitative agreement with experimental results. Failure to achieve complete removal of HT from the cold column effluent as predicted was ascribed to the finite rates of the exchange reaction and to the presence and operation of an isotope effect in the rate of hydrogen absorption.

Wong, Y.W.; Chan, Y.N.I.; Hill, F.B.

1979-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "laser isotope separation" 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

ANALYSIS AND OPTIMIZATION OF GAS- CENTRIFUGAL SEPARATION OF URANIUM ISOTOPES BY NEURAL NETWORKS  

E-Print Network (OSTI)

Abstract- Neural networks are an attractive alternative for modeling complex problems with too many difficulties to be solved by a phenomenological model. A feed-forward neural network was used to model a gas-centrifugal separation of uranium isotopes. The prediction showed good agreement with the experimental data. An optimization study was carried out. The optimal operational condition was tested by a new experiment and a difference of less than 1 % was found.

unknown authors

2002-01-01T23:59:59.000Z

82

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

Science Conference Proceedings (OSTI)

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

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

2009-03-29T23:59:59.000Z

83

A Transient Model of Induced Natural Circulation Thermal Cycling for Hydrogen Isotope Separation  

SciTech Connect

The property of selective temperature dependence of adsorption and desorption of hydrogen isotopes by palladium is used for isotope separation. A proposal to use natural circulation of nitrogen to alternately heat and cool a packed bed of palladium coated beads is under active investigation, and a device consisting of two interlocking natural convection loops is being designed. A transient numerical model of the device has been developed to aid the design process. It is a one-dimensional finite-difference model, using the Boussinesq approximation. The thermal inertia of the pipe walls and other heat structures as well as the heater control logic is included in the model. Two system configurations were modeled and results are compared.

SHADDAY, MARTIN

2005-07-12T23:59:59.000Z

84

High-power semiconductor separate-confinement double heterostructure lasers  

Science Conference Proceedings (OSTI)

The review is devoted to high-power semiconductor lasers. Historical reference is presented, physical and technological foundations are considered, and the concept of high-power semiconductor lasers is formulated. Fundamental and technological reasons limiting the optical power of a semiconductor laser are determined. The results of investigations of cw and pulsed high-power semiconductor lasers are presented. Main attention is paid to inspection of the results of experimental studies of single high-power semiconductor lasers. The review is mainly based on the data obtained in the laboratory of semiconductor luminescence and injection emitters at the A.F. Ioffe Physicotechnical Institute. (review)

Tarasov, I S [A.F. Ioffe Physical-Technical Institute, Russian Academy of Sciences, St. Petersburg (Russian Federation)

2010-10-15T23:59:59.000Z

85

Infrared laser system  

DOE Patents (OSTI)

An infrared laser system and method for isotope separation may comprise a molecular gas laser oscillator to produce a laser beam at a first wavelength, Raman spin flip means for shifting the laser to a second wavelength, a molecular gas laser amplifier to amplify said second wavelength laser beam to high power, and optical means for directing the second wavelength, high power laser beam against a desired isotope for selective excitation thereof in a mixture with other isotopes. The optical means may include a medium which shifts the second wavelength high power laser beam to a third wavelength, high power laser beam at a wavelength coincidental with a corresponding vibrational state of said isotope and which is different from vibrational states of other isotopes in the gas mixture.

Cantrell, Cyrus D. (Santa Fe, NM); Carbone, Robert J. (Los Alamos, NM); Cooper, Ralph S. (Los Alamos, NM)

1977-01-01T23:59:59.000Z

86

Infrared laser system  

DOE Patents (OSTI)

An infrared laser system and method for isotope separation may comprise a molecular gas laser oscillator to produce a laser beam at a first wavelength, Raman spin flip means for shifting the laser to a second wavelength, a molecular gas laser amplifier to amplify said second wavelength laser beam to high power, and optical means for directing the second wavelength, high power laser beam against a desired isotope for selective excitation thereof in a mixture with other isotopes. The optical means may include a medium which shifts the second wavelength high power laser beam to a third wavelength, high power laser beam at a wavelength coincidental with a corresponding vibrational state of said isotope and which is different from vibrational states of other isotopes in the gas mixture.

Cantrell, Cyrus D. (Richardson, TX); Carbone, Robert J. (Johnson City, TN); Cooper, Ralph (Hayward, CA)

1982-01-01T23:59:59.000Z

87

NATIONAL USES AND NEEDS FOR SEPARATED STABLE ISOTOPES IN PHYSICS, CHEMISTRY, AND GEOSCIENCE RESEARCH  

E-Print Network (OSTI)

York, K. Rankama, Isotope Geology, McGraw-Hill, New York,geochronometry and isotope geology. elements report. ofisotopes were utilized in the research areas and geology,

Zisman, M.S.

2010-01-01T23:59:59.000Z

88

Laser vaporization/ionization interface for coupling microscale separation techniques with mass spectrometry  

DOE Patents (OSTI)

The present invention provides a laser-induced vaporization and ionization interface for directly coupling microscale separation processes to a mass spectrometer. Vaporization and ionization of the separated analytes are facilitated by the addition of a light-absorbing component to the separation buffer or solvent. 8 figs.

Yeung, E.S.; Chang, Y.C.

1999-06-29T23:59:59.000Z

89

RADIATION STABILITY OF NAFION MEMBRANES USED FOR ISOTOPE SEPARATION BY PROTON EXCHANGE MEMBRANE ELECTROLYSIS  

Science Conference Proceedings (OSTI)

Proton Exchange Membrane Electrolyzers have potential interest for use for hydrogen isotope separation from water. In order for PEME to be fully utilized, more information is needed on the stability of Nafion when exposed to radiation. This work examines Nafion 117 under varying exposure conditions, including dose rate, total dosage and atmospheric condition. Analytical tools, such as FT-IR, ion exchange capacity, DMA and TIC-TOC were used to characterize the exposed membranes. Analysis of the water from saturated membranes can provide important data on the stability of the membranes during radiation exposure. It was found that the dose rate of exposure plays an important role in membrane degradation. Potential mechanisms for membrane degradation include peroxide formation by free radicals.

Fox, E

2009-05-15T23:59:59.000Z

90

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

91

arXiv:1001.0944v2[physics.atom-ph]7May2010 Single-Photon Atomic Sorting: Isotope Separation with Maxwell's Demon  

E-Print Network (OSTI)

- ods of separation are gaseous diffusion and the ultra- centrifuge [1­3]. These methods require many elements that can be kept in gas phase, which is a common limitation of isotope separation schemes [4

Texas at Austin. University of

92

Validation of Electrochemically Modulated Separations Performed On-Line with MC-ICP-MS for Uranium and Plutonium Isotopic Analyses  

Science Conference Proceedings (OSTI)

The most time consuming process in uranium or plutonium isotopic analyses is performing the requisite chromatographic separation of the actinides. Filament preparation for thermal ionization (TIMS) adds further delays, but is generally accepted due to the unmatched performance in trace isotopic analyses. Advances in Multi-Collector Inductively Coupled Plasma Mass Spectrometry (MC-ICP-MS) are beginning to rival the performance of TIMS. Methods, such as Electrochemically Modulated Separations (EMS) can efficiently pre-concentrate U or Pu quite selectively from small solution volumes in a matrix of 0.5 M nitric acid. When performed in-line with ICP-MS, the rapid analyte release from the electrode is fast, and large transient analyte signal enhancements of >100 fold can be achieved as compared to more conventional continuous nebulization of the original starting solution. This makes the approach ideal for very low level isotope ratio measurements. In this paper, some aspects of EMS performance are described. These include low level Pu isotope ratio behavior versus concentration by MC-ICP-MS and uranium rejection characteristics that are also important for reliable low level Pu isotope ratio determinations.

Liezers, Martin; Olsen, Khris B.; Mitroshkov, Alexandre V.; Duckworth, Douglas C.

2010-08-11T23:59:59.000Z

93

Sulfur stable isotopes separate producers in marine food-web analysis  

Science Conference Proceedings (OSTI)

Fry B (1983) Fish and shrimp migrations in the northern Gulf of. Mexico analysed using stable C, N and S isotope ratios. Fish. Bull 81:789–801. Fry B (1988) ...

94

Improvement of Pt/C/PTFE catalyst type used for hydrogen isotope separation  

Science Conference Proceedings (OSTI)

The CANDU reactor from the Nuclear Power plant Cernavoda (Romania)) is the most powerful tritium source from Europe. This reactor is moderated and cooled by heavy water that becomes continuously contaminated with tritium. Because of this reason, the National R and amp;D Inst. for Cryogenic and Isotopic Technologies developed a detritiation technology based on catalytic isotopic exchange and cryogenic distillation. The main effort of our Inst. was focused on finding more efficient catalysts with a longer operational life. Some of the tritium removal processes involved in Fusion Science and Technology use this type of catalyst 1. Several Pt/C/PTFE hydrophobic catalysts that could be used in isotopic exchange process 2,3,4 were produced. The present paper presents a comparative study between the physical and morphological properties of different catalysts manufactured by impregnation at our institute. The comparison consists of a survey of specific surface, pores volume and pores distribution. (authors)

Vasut, F.; Preda, A.; Zamfirache, M.; Bornea, A. M.; Stefanescu, I.; Pearsica, C. [INC-DTCI, ICSI Rm. Valcea, Uzinei Street 4, Rm. Valcea (Romania)

2008-07-15T23:59:59.000Z

95

Determination of Plutonium Isotope Ratios at Very Low Levels by ICP-MS using On-Line Electrochemically Modulated Separations  

Science Conference Proceedings (OSTI)

Electrochemically modulated separations (EMS) are shown to be a rapid and selective means of extracting and concentrating Pu from complex solutions prior to isotopic analysis by inductively coupled plasma mass spectrometry (ICP?MS). This separation is performed in a flow injection mode, on?line with the ICP?MS. A three?electrode, flow?by electrochemical cell is used to accumulate Pu at an anodized glassy carbon electrode by redox conversion of Pu(III) to Pu (IV&VI). The entire process takes place in 2% v/v (0.46M) HNO3. No redox chemicals or acid concentration changes are required. Plutonium accumulation and release is redox dependent and controlled by the applied cell potential. Thus large transient volumetric concentration enhancements can be achieved. Based on more negative U(IV) potentials relative to Pu(IV), separation of Pu from uranium is efficient, thereby eliminating uranium hydride interferences. EMS?ICP?MS isotope ratio measurement performance will be presented for femtogram to attogram level plutonium concentrations.

Liezers, Martin; Lehn, Scott A.; Olsen, Khris B.; Farmer, Orville T.; Duckworth, Douglas C.

2009-10-01T23:59:59.000Z

96

ISOTOPES  

E-Print Network (OSTI)

depends on the cost and energy efficiency of the laser.and the low cost and energy efficiency of existing, large-

Lederer, C. Michael

2013-01-01T23:59:59.000Z

97

Isotopic separation of sup 3 He/ sup 4 He from solar wind gases evolved from the lunar regolith  

Science Conference Proceedings (OSTI)

The potential benefits of {sup 3}He when utilized in a nuclear fusion reactor to provide clean, safe electricity in the 21st century for the world's inhabitants has been documented. Unfortunately, He is scarce on earth. Large quantities of {sup 3}He, perhaps a million tonnes, are embedded in the lunar regolith, presumably implanted by the solar wind together with other elements, notably {sup 4}He, H, C and N. Several studies have suggested processing the lunar regolith and recovering these valuable solar wind gases. Once released, these gases can be separated for use. The separation of helium isotopes is described in this paper. {sup 3}He constitutes only 400 at{center dot}ppm of lunar He, too dilute to separate economically by distillation alone. A superfluid'' separator is being considered to preconcentrate the {sup 3}He. The superfluid separator consists of a porous filter in a tube maintained at a temperature of 2.17 K or less. Although the {sup 4}He, which is superfluid below 2.17 K, flows readily through the filter, the He is blocked by the filter, and becomes enriched at the feed end. He can be enriched to about 10% in such a system. The enriched product from the superfluid separation serves as a feed to a distillation apparatus operating at a pressure of 9 kPa, with a boiler temperature of 2.4 K, and a condenser temperature of 1.6 K. Under constant flow conditions, a 99.9% enriched He product can be produced in this apparatus. The heat rejection load of the refrigeration equipment necessary to cool the separation operations would be conducted during the lunar nights.

Wilkes, W.R. (EG and G Mound Applied Technologies, Miamisburg, OH (United States)); Wittenberg, L.J. (Wisconsin Univ., Madison, WI (United States))

1992-01-01T23:59:59.000Z

98

Isotopic separation of {sup 3}He/{sup 4}He from solar wind gases evolved from the lunar regolith  

Science Conference Proceedings (OSTI)

The potential benefits of {sup 3}He when utilized in a nuclear fusion reactor to provide clean, safe electricity in the 21st century for the world`s inhabitants has been documented. Unfortunately, He is scarce on earth. Large quantities of {sup 3}He, perhaps a million tonnes, are embedded in the lunar regolith, presumably implanted by the solar wind together with other elements, notably {sup 4}He, H, C and N. Several studies have suggested processing the lunar regolith and recovering these valuable solar wind gases. Once released, these gases can be separated for use. The separation of helium isotopes is described in this paper. {sup 3}He constitutes only 400 at{center_dot}ppm of lunar He, too dilute to separate economically by distillation alone. A ``superfluid`` separator is being considered to preconcentrate the {sup 3}He. The superfluid separator consists of a porous filter in a tube maintained at a temperature of 2.17 K or less. Although the {sup 4}He, which is superfluid below 2.17 K, flows readily through the filter, the He is blocked by the filter, and becomes enriched at the feed end. He can be enriched to about 10% in such a system. The enriched product from the superfluid separation serves as a feed to a distillation apparatus operating at a pressure of 9 kPa, with a boiler temperature of 2.4 K, and a condenser temperature of 1.6 K. Under constant flow conditions, a 99.9% enriched He product can be produced in this apparatus. The heat rejection load of the refrigeration equipment necessary to cool the separation operations would be conducted during the lunar nights.

Wilkes, W.R. [EG and G Mound Applied Technologies, Miamisburg, OH (United States); Wittenberg, L.J. [Wisconsin Univ., Madison, WI (United States)

1992-09-01T23:59:59.000Z

99

Isotope effects in the harmonic response from hydrogenlike muonic atoms in strong laser fields  

SciTech Connect

High-order harmonic generation from hydrogenlike muonic atoms exposed to ultraintense high-frequency laser fields is studied. Systems of low nuclear-charge number Z are considered where a nonrelativistic description applies. By comparing the radiative response for different isotopes, we demonstrate characteristic signatures of the finite nuclear mass and size in the harmonic spectra. In particular, for Z>1, an effective muon charge appears in the Schroedinger equation for the relative particle motion, which influences the position of the harmonic cutoff. Cutoff energies in the million-electron-volt domain can be achieved, offering prospects for the generation of ultrashort coherent {gamma}-ray pulses.

Shahbaz, Atif; Mueller, Carsten [Max-Planck-Institut fuer Kernphysik, Saupfercheckweg 1, D-69117 Heidelberg (Germany); Buervenich, Thomas J. [Frankfurt Institute for Advanced Studies, Johann Wolfgang Goethe University, Ruth-Moufang-Strasse 1, D-60438 Frankfurt am Main (Germany)

2010-07-15T23:59:59.000Z

100

An apparatus for studies of hydrogen isotope exchange over metals using laser-Raman spectroscopy  

DOE Green Energy (OSTI)

An apparatus that uses laser-Raman spectroscopy measures the dynamic gas composition and pressure of mixed hydrogen isotopes as they exchange over hydride-forming metals or alloys. Data for the exchange of protium and deuterium over ZrCo alloy at 260{degree}C indicate that this alloy begins exchanging at temperatures only slightly above room temperature and rapidly and completely exchanges at the higher temperature. The method is suitable for studies of bulk hydrogen/metal interactions. 10 refs., 3 figs.

Carstens, D.H.W.

1990-10-01T23:59:59.000Z

Note: This page contains sample records for the topic "laser isotope separation" 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

Continuous production of tritium in an isotope-production reactor with a separate circulation system  

DOE Patents (OSTI)

A method is described for producing tritium in a fast breeder reactor cooled with liquid metal. Lithium is allowed to flow through the reactor in separate loops in order to facilitate the production and removal of tritium.

Cawley, W.E.; Omberg, R.P.

1982-08-19T23:59:59.000Z

102

Characterization of Diesel Fuel by Chemical Separation Combined with Capillary Gas Chromatography (GC) Isotope Ratio Mass Spectrometry (IRMS)  

Science Conference Proceedings (OSTI)

The purpose of this study was to perform a preliminary investigation of compound-specific isotope analysis (CSIA) of diesel fuels to evaluate whether the technique could distinguish between the diesel samples from different sources/locations. The ability to differentiate or correlate diesel samples could be valuable for detecting fuel tax evasion schemes. Two fractionation techniques were used to isolate the n-alkanes from the fuel. Both ?13C and ?D values for the n-alkanes were then determined by CSIA in each sample. Plots of ?D versus ?13C with sample n-alkane points connected in order of increasing carbon number gave well separated clusters with characteristic shapes for each sample. Principal components analysis (PCA) with ?13C, ?D, or combined ?13C and ?D data on the yielded scores plots that could clearly differentiate the samples, thereby demonstrating the potential of this approach for fingerprinting fuel samples using the ?13C and ?D values.

Harvey, Scott D.; Jarman, Kristin H.; Moran, James J.; Sorensen, Christina M.; Wright, Bob W.

2011-09-15T23:59:59.000Z

103

Recent developments of the ion sources at Tri University Meson Factory/Isotope Separator and ACcelerator Facility  

SciTech Connect

This paper describes the recent progresses concerning the on-line ion source at the Tri University Meson Factory/Isotope Separator and ACcelerator (TRIUMF/ISAC) Radioactive Ion-Beam Facility; description of the new design of the surface-ion-source for improved stability of the beam intensity, description of the transport path to the east target station at ISAC, description of the new brazing techniques that solved recurrent problems with water leaks on the target/ion source assembly in the vacuum system, finally, recent developments concerning the Forced Electron Beam Induced Arc Discharge (FEBIAD) ion source are reported. In particular, a study on the effect of the plasma chamber volume on the ionization efficiency was completed.

Bricault, P. G.; Ames, F.; Dombsky, M.; Labrecque, F.; Lassen, J.; Mjos, A.; Minor, G. [TRIUMF, 4004 Wesbrook Mall, Vancouver, British Columbia V6T 2A3 (Canada); Tigelhoefer, A. [TRIUMF, 4004 Wesbrook Mall, Vancouver, British Columbia V6T 2A3 (Canada); Department Of Physics, University of Manitoba, Winnipeg, Manitoba R3T 2N2 (Canada)

2012-02-15T23:59:59.000Z

104

Sensitive multi-photon nonlinear laser spectroscopic methods for isotope analysis in atmospheric and environmental applications  

E-Print Network (OSTI)

isotopic spectra of atomic chlorine with its two naturallythese applications. Figure 2.4 Chlorine isotope ratios inIsotope Measurements of Atomic Chlorine Using a Low-Pressure

Lyons, Wendy Jean

2009-01-01T23:59:59.000Z

105

Isotopic imaging via nuclear resonance fluorescence with laser-based Thomson radiation  

DOE Patents (OSTI)

The present invention utilizes novel laser-based, high-brightness, high-spatial-resolution, pencil-beam sources of spectrally pure hard x-ray and gamma-ray radiation to induce resonant scattering in specific nuclei, i.e., nuclear resonance fluorescence. By monitoring such fluorescence as a function of beam position, it is possible to image in either two dimensions or three dimensions, the position and concentration of individual isotopes in a specific material configuration. Such methods of the present invention material identification, spatial resolution of material location and ability to locate and identify materials shielded by other materials, such as, for example, behind a lead wall. The foundation of the present invention is the generation of quasimonochromatic high-energy x-ray (100's of keV) and gamma-ray (greater than about 1 MeV) radiation via the collision of intense laser pulses from relativistic electrons. Such a process as utilized herein, i.e., Thomson scattering or inverse-Compton scattering, produces beams having diameters from about 1 micron to about 100 microns of high-energy photons with a bandwidth of .DELTA.E/E of approximately 10E.sup.-3.

Barty, Christopher P. J. (Hayward, CA); Hartemann, Frederic V. (San Ramon, CA); McNabb, Dennis P. (Alameda, CA); Pruet, Jason A. (Brentwood, CA)

2009-07-21T23:59:59.000Z

106

Research proposal on certain atomic physics measurements associated with the laser isotope separation method  

SciTech Connect

Research proposed in the following areas are briefly described: the measurement of photoionization cross sections near threshold for the excited states of uranium; measurement of the symmetric charge exchange cross section; and measurement of chemiionization cross sections for electronically excited uranium atoms.

Dubrin, J.; Duewer, W.

1973-03-06T23:59:59.000Z

107

A Mass Spectrometry Study of Isotope Separation in the Laser Plume  

E-Print Network (OSTI)

Attribution and Non-Proliferation Applications”, IEEETreaty on the Non-Proliferation of Nuclear Weapons (NPT)”,as detailed in the Non-Proliferation Treaty (NPT), is to

Suen, Timothy Wu

2012-01-01T23:59:59.000Z

108

A Mass Spectrometry Study of Isotope Separation in the Laser Plume  

E-Print Network (OSTI)

Proliferation of Nuclear Weapons (NPT)”, http: //www.un.org/end of the Cold War, nuclear weapons remain at the heart ofthe spread of nuclear weapons, analysis of nuclear materials

Suen, Timothy Wu

2012-01-01T23:59:59.000Z

109

A Mass Spectrometry Study of Isotope Separation in the Laser Plume  

E-Print Network (OSTI)

as detailed in the Non-Proliferation Treaty (NPT), is toUnited Nations, “Treaty on the Non-Proliferation of Nuclear

Suen, Timothy Wu

2012-01-01T23:59:59.000Z

110

A Mass Spectrometry Study of Isotope Separation in the Laser Plume  

E-Print Network (OSTI)

Pakistan is exacerbated by concerns over both terrorist activity and the security of its rapidly increasing nuclear

Suen, Timothy Wu

2012-01-01T23:59:59.000Z

111

Brief history of the Los Alamos laser programs  

SciTech Connect

The laser programs at Los Alamos began in 1969 to investigate the feasibility of laser-induced fusion. However, within a year they had been expanded to include a number of other applications including laser isotope separation. These programs now compose a substantial part of the Laboratory's research programs.

Boyer, K.

1983-01-01T23:59:59.000Z

112

Research Directed at Developing a Classical Theory to Describe Isotope Separation of Polyatomic Molecules Illuminated by Intense Infrared Radiation. Final Report for period May 7, 1979 to September 30, 1979; Extension December 31, 1997  

DOE R&D Accomplishments (OSTI)

This final report describes research on the theory of isotope separation produced by the illumination of polyatomic molecules by intense infrared laser radiation. This process is investigated by treating the molecule, sulfur hexafluoride, as a system of seven classical particles that obey the Newtonian equations of motion. A minicomputer is used to integrate these differential equations. The particles are acted on by interatomic forces, and by the time-dependent electric field of the laser. We have a very satisfactory expression for the interaction of the laser and the molecule which is compatible with infrared absorption and spectroscopic data. The interatomic potential is capable of improvement, and progress on this problem is still being made. We have made several computer runs of the dynamical behavior of the molecule using a reasonably good model for the interatomic force law. For the laser parameters chosen, we find that typically the molecule passes quickly through the resonance region into the quasi-continuum and even well into the real continuum before dissociation actually occurs. When viewed on a display terminal, the motions are exceedingly complex. As an aid to the visualization of the process, we have made a number of 16 mm movies depicting a three-dimensional representation of the motion of the seven particles. These show even more clearly the enormous complexity of the motions, and make clear the desirability of finding ways of characterizing the motion in simple ways without giving all of the numerical detail. One of the ways to do this is to introduce statistical parameters such as a temperature associated with the distribution of kinetic energies of the single particle. We have made such an analysis of our data runs, and have found favorable indications that such methods will prove useful in keeping track of the dynamical histories.

Lamb, W. E. Jr.

1981-12-00T23:59:59.000Z

113

Analysis of hydrogen isotope mixtures  

DOE Patents (OSTI)

Disclosed are an apparatus and a method for determining concentrations of hydrogen isotopes in a sample. Hydrogen in the sample is separated from other elements using a filter selectively permeable to hydrogen. Then the hydrogen is condensed onto a cold finger or cryopump. The cold finger is rotated as pulsed laser energy vaporizes a portion of the condensed hydrogen, forming a packet of molecular hydrogen. The desorbed hydrogen is ionized and admitted into a mass spectrometer for analysis.

Villa-Aleman, E.

1992-12-31T23:59:59.000Z

114

Analysis of hydrogen isotope mixtures  

DOE Patents (OSTI)

An apparatus and method for determining the concentrations of hydrogen isotopes in a sample. Hydrogen in the sample is separated from other elements using a filter selectively permeable to hydrogen. Then the hydrogen is condensed onto a cold finger or cryopump. The cold finger is rotated as pulsed laser energy vaporizes a portion of the condensed hydrogen, forming a packet of molecular hydrogen. The desorbed hydrogen is ionized and admitted into a mass spectrometer for analysis.

Villa-Aleman, Eliel (Aiken, SC)

1994-01-01T23:59:59.000Z

115

Laser programs highlights 1993  

SciTech Connect

Over the last two decades, the scope of our laser research has grown immensely. The small, low-power laser systems of our early days have given way to laser systems of record-breaking size and power. Now we are focusing our activities within the target physics and laser science programs to support the ignition and gain goals of the proposed glass-laser National Ignition Facility. In our laser isotope separation work, we completed the most important set of experiments in the history of the AVLIS Program in 1993, which culminated in a spectacularly successful run that met or exceeded all our objectives. We are also developing lasers and laser-related technologies for a variety of energy, commercial, and defense uses. On the horizon are transfers of important technologies for waste treatment, x-ray lithography, communications and security, optical imaging, and remote sensing, among others.

NONE

1995-06-01T23:59:59.000Z

116

Isotope Enrichment | ornl.gov  

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

Modern electromagnetic isotope separator developed and being scaled-up to replace the Manhattan Project-era Calutrons used for stable isotope enrichment. Since 1945, ORNL has...

117

Quantifying Uranium Isotope Ratios Using Resonance Ionization Mass Spectrometry: The Influence of Laser Parameters on Relative Ionization Probability  

E-Print Network (OSTI)

4.5 Uranium Isotope Ratio Measurements . . . . . .4.32 Uranium sputtered from three U-rich materials of varying uranium isotopic

Isselhardt, Brett Hallen

2011-01-01T23:59:59.000Z

118

Search for the gamma-branch of the shape isomers of separated U isotopes using muon for nuclide excitation  

SciTech Connect

We have searched for back-decay gamma rays from the shape isomeric states in /sup 235/U, /sup 236/U, and /sup 238/U possibly excited in muon radiationless transition. The energies and intensities of gamma rays following muon atomic capture were measured as a function of time after muon stopping. Background was suppressed by requiring that the candidate gamma ray be followed by another gamma ray (..mu..-capture gamma ray). The prompt gamma-ray spectra included the U-muonic x rays. The measured /sup 235/U and /sup 238/U x-ray energies were in good agreement with previously reported results. The x-ray spectrum from /sup 236/U has not been previously reported. The /sup 236/U spectrum is very similar to that of /sup 238/U, except that the K x-rays exhibit an isotope shift of approximately 20 keV, the /sup 236/U energies being higher. In the analysis of the delayed spectra of /sup 236/U and /sup 238/U using the GAMANL peak searching program, and with an effective lower-limit detection efficiency of .15% per stopping muon, no candidate gamma rays for the back decay transitions from the shape isomeric state were observed.

Mireshghi, A.

1982-12-01T23:59:59.000Z

119

Isotope Shift Measurements of Stable and Short-Lived Lithium Isotopes for Nuclear Charge Radii Determination  

E-Print Network (OSTI)

Changes in the mean-square nuclear charge radii along the lithium isotopic chain were determined using a combination of precise isotope shift measurements and theoretical atomic structure calculations. Nuclear charge radii of light elements are of high interest due to the appearance of the nuclear halo phenomenon in this region of the nuclear chart. During the past years we have developed a new laser spectroscopic approach to determine the charge radii of lithium isotopes which combines high sensitivity, speed, and accuracy to measure the extremely small field shift of an 8 ms lifetime isotope with production rates on the order of only 10,000 atoms/s. The method was applied to all bound isotopes of lithium including the two-neutron halo isotope Li-11 at the on-line isotope separators at GSI, Darmstadt, Germany and at TRIUMF, Vancouver, Canada. We describe the laser spectroscopic method in detail, present updated and improved values from theory and experiment, and discuss the results.

Nörtershäuser, W; Ewald, G; Dax, A; Behr, J; Bricault, P; Bushaw, B A; Dilling, J; Dombsky, M; Drake, G W F; Götte, S; Kluge, H -J; Kühl, Th; Lassen, J; Levy, C D P; Pachucki, K; Pearson, M; Puchalski, M; Wojtaszek, A; Yan, Z -C; Zimmermann, C

2010-01-01T23:59:59.000Z

120

Alcohol fuel use: Implications for atmospheric levels of aldehydes, organic nitrates, pans, and peroxides: Separating sources using carbon isotopes  

DOE Green Energy (OSTI)

We have developed DiNitroPhenylHydrazone (DNPH) derivatization--high performance liquid chromatographic methods for measuring aldehydes in ambient samples with detection limits of approximately 1ppbV. These methods can be used for air or precipitation studies, and have been used for indoor measurements at much higher levels using shorter integration times. We are using gas chromatographs with electron capture detection (GCECD) to measure ambient levels of peroxyacyl nitrates and organic nitrates. Diffusion tubes with synthetically produced organic nitrates in n-tridecane solution are used to calibrate these systems. These compounds are important means of transporting NO/sub x/ over large scales due to their reduced tropospheric reactivity, low water solubilities, photolytic, and thermal stability. Their chemistries are coupled to aldehyde chemistry and are important greenhouse gases as well as phytotoxins. We have completed preliminary studies in Rio de Janeiro examining the atmospheric chemistry consequences of ethanol fuel usage. The urban air mass has been effected by the direct uncontrolled usage of ethanolgasoline and ethanoldiesel mixtures. We are exploring the use of luminol chemiluminescent detection of peroxides using gas chromatography to separate the various organic and inorganic peroxides. These compounds are coupled to the aldehyde chemistry, particularly in remote chemistries down-wind of urban sources. 13 refs.

Gaffney, J.S.; Tanner, R.L.

1988-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "laser isotope separation" 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

Quantifying Uranium Isotope Ratios Using Resonance Ionization Mass Spectrometry: The Influence of Laser Parameters on Relative Ionization Probability  

E-Print Network (OSTI)

a laser system intended to make reproducible measurements ofof uranium measurements. The new laser system should be used

Isselhardt, Brett Hallen

2011-01-01T23:59:59.000Z

122

Isotope-selective laser molecular alignment Sharly Fleischer, I. Sh. Averbukh, and Yehiam Prior*  

E-Print Network (OSTI)

and centrifuge-based separation methods rely on generic mechanical effects caused by small mass differences a wide range of topics to be studied. In the gas phase, molecular alignment follow- ing excitation that of an isotropic gas was monitored as evidence for alignment 14,15 . More recently, these observations have been

Prior, Yehiam

123

Mantle helium and carbon isotopes in Separation Creek Geothermal Springs, Three Sisters area, Central Oregon: Evidence for renewed volcanic activity or a long term steady state system?  

DOE Green Energy (OSTI)

Cold bubbling springs in the Separation Creek area, the locus of current uplift at South Sister volcano show strong mantle signatures in helium and carbon isotopes and CO{sub 2}/{sup 3}He. This suggests the presence of fresh basaltic magma in the volcanic plumbing system. Currently there is no evidence to link this system directly to the uplift, which started in 1998. To the contrary, all geochemical evidence suggests that there is a long-lived geothermal system in the Separation Creek area, which has not significantly changed since the early 1990s. There was no archived helium and carbon data, so a definite conclusion regarding the strong mantle signature observed in these tracers cannot yet be drawn. There is a distinct discrepancy between the yearly magma supply required to explain the current uplift (0.006 km{sup 3}/yr) and that required to explain the discharge of CO{sub 2} from the system (0.0005 km{sup 3}/yr). This discrepancy may imply that the chemical signal associated with the increase in magma supply has not reached the surface yet. With respect to this the small changes observed at upper Mesa Creek require further attention, due to the recent volcanic vent in that area it may be the location were the chemical signal related to the uplift can most quickly reach the surface. Occurrence of such strong mantle signals in cold/diffuse geothermal systems suggests that these systems should not be ignored during volcano monitoring or geothermal evaluation studies. Although the surface-expression of these springs in terms of heat is minimal, the chemistry carries important information concerning the size and nature of the underlying high-temperature system and any changes taking place in it.

van Soest, M.C.; Kennedy, B.M.; Evans, W.C.; Mariner, R.H.

2002-04-30T23:59:59.000Z

124

Nucleon-induced fission cross-sections of tantalum and separated tungsten isotopes and "compound nucleus" effect in intermediate energy region  

E-Print Network (OSTI)

Neutron- and proton-induced fission cross-sections of separated isotopes of tungsten (182W, 183W, 184W, and 186W) and 181Ta relative to 209Bi have been measured in the incident nucleon energy region 50 - 200 MeV using fission chambers based on thin-film breakdown counters (TFBC) using quasi-monoenergetic neutrons from the 7Li(p,n) reaction and at the proton beams of The Svedberg Laboratory (TSL), Uppsala University (Uppsala, Sweden). The results are compared with predictions by the CEM03.01 event generator, as well as with the recent data for nuclei in the lead-bismuth region. The effect of "compound nucleus" in the intermediate energy region is discussed, displaying in exponential dependence of nucleon-induced fission cross-sections on the parameter Z^2/A of the composite system (projectile+target nucleus), and in other characteristics of the fission process for which parameter Z^2/A plays a role similar to the one of the usual liquid-drop parameter Z^2/A of compound nuclei.

A. N. Smirnov; O. I. Batenkov; V. P. Eismont; N. P. Filatov; J. Blomgren; H. Conde; A. V. Prokofiev; S. G. Mashnik

2007-05-16T23:59:59.000Z

125

A New Hydrophobic Catalyst for Tritium Separation from Nuclear Effluents  

Science Conference Proceedings (OSTI)

Technical Paper / Tritium Science and Technology - Tritium Science and Technology - Detritiation, Purification, and Isotope Separation

I. Popescu; Gh. Ionita; I. Stefanescu; A. Kitamoto

126

Optical isotope shift and hyperfine structure measurements in preparation of the ultra-sensitive detection of krypton atoms using stepwise laser excitation and field ionization  

E-Print Network (OSTI)

Within the scope of the ultra sensitive detection project the operation of the collinear fast beam laser spectroscopy apparatus and data acquisition was learned and optimized with respect to the reduction of stray laser light and the charge exchange process. Major contributions to fluctuations and drifts in the measurements have been investigated. The present data is evaluated using only the relativistically correct expressions with Microcal ORIGIN and the IMSL subroutines to perform a least squares fit to the hyperfine structure data when evaluating the hyperfine structure constants A and B. The results are the hyperfinestructure constants and isotope shifts in two transitions from the 5s'[1/2]0' , IS3 , and three transitions from the 5s[3/212' , I S5 , metastable state of krypton. The results of the isotope shift measurements in the 892 nm line of Kr have not been published previously. For the further development of the trace detection of Kr isotopes the work resulted in the construction and installation of the necessary ion-optics and detectors. Changes have been prepared as a result of the ongoing measurements. These are quasicollinear excitation of the Kr beam, avoiding optical pumping and stark shifts, shortening the distance between optical excitation and field ionization and foremost a two order of magnitude improvement of the vacuum conditions in the region the Rydberg atoms traverse by differential pumping. The overall project goal of two step resonant excitation and field ionization seems to be in close reach .

Lassen, Jens

1996-01-01T23:59:59.000Z

127

CONTROL FOR ISOTOPE SEPARATING APPARATUS  

DOE Patents (OSTI)

Improvements in methods and means for controlling the position and condition of the ion beam of calutrons for more efficient operation were developed. These improvements were accomplished by the addition of a new electrode in the receiver adjacent to and on the far side of one of the ion collector pockets. this electrode receiving and metering a small pcrtion of the outer fringe of the ion beam directed to this pocket. More sensitive and accurate control of the focusing of the ion beams may be obtained by maximizing the ratio of the current to the above pocket to the current to the additional electrode.

Brackney, H.W.

1960-08-01T23:59:59.000Z

128

Isotope-shift measurements of stable and short-lived lithium isotopes for nuclear-charge-radii determination  

Science Conference Proceedings (OSTI)

Changes in the mean square nuclear charge radii along the lithium isotopic chain were determined using a combination of precise isotope shift measurements and theoretical atomic structure calculations. Nuclear charge radii of light elements are of high interest due to the appearance of the nuclear halo phenomenon in this region of the nuclear chart. During the past years we have developed a laser spectroscopic approach to determine the charge radii of lithium isotopes which combines high sensitivity, speed, and accuracy to measure the extremely small field shift of an 8-ms-lifetime isotope with production rates on the order of only 10 000 atoms/s. The method was applied to all bound isotopes of lithium including the two-neutron halo isotope {sup 11}Li at the on-line isotope separators at GSI, Darmstadt, Germany, and at TRIUMF, Vancouver, Canada. We describe the laser spectroscopic method in detail, present updated and improved values from theory and experiment, and discuss the results.

Noertershaeuser, W.; Sanchez, R. [GSI Helmholtzzentrum fuer Schwerionenforschung GmbH, D-64291 Darmstadt (Germany); Institut fuer Kernchemie, Universitaet Mainz, D-55099 Mainz (Germany); Ewald, G.; Dax, A.; Goette, S.; Kluge, H.-J.; Kuehl, Th.; Wojtaszek, A. [GSI Helmholtzzentrum fuer Schwerionenforschung GmbH, D-64291 Darmstadt (Germany); Behr, J.; Bricault, P.; Dilling, J.; Dombsky, M.; Lassen, J.; Levy, C. D. P.; Pearson, M. [TRIUMF, Vancouver, British Columbia, V6T 2A3 (Canada); Bushaw, B. A. [Pacific Northwest National Laboratory, Richland, Washington 99352 (United States); Drake, G. W. F. [Department of Physics, University of Windsor, Windsor, Ontario, N9B 3P4 (Canada); Pachucki, K. [Faculty of Physics, University of Warsaw, PL-00-681 Warsaw (Poland); Puchalski, M. [Faculty of Chemistry, Adam Mickiewicz University, Grunwaldzka 6, PL-60-780 Poznan (Poland); Yan, Z.-C. [Department of Physics, University of New Brunswick, Fredericton, New Brunswick, E3B 5A3 (Canada)

2011-01-15T23:59:59.000Z

129

ISOTOPE CONVERSION DEVICE  

DOE Patents (OSTI)

This patent relates to nuclear reactors of tbe type utilizing a liquid fuel and designed to convert a non-thermally fissionable isotope to a thermally fissionable isotope by neutron absorption. A tank containing a reactive composition of a thermally fissionable isotope dispersed in a liquid moderator is disposed within an outer tank containing a slurry of a non-thermally fissionable isotope convertible to a thermally fissionable isotope by neutron absorption. A control rod is used to control the chain reaction in the reactive composition and means are provided for circulating and cooling the reactive composition and slurry in separate circuits.

Wigner, E.P.; Young, G.J.; Ohlinger, L.A.

1957-12-01T23:59:59.000Z

130

Isotope Development & Production | Nuclear Science | ORNL  

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

Medical Radioisotope Radiochemical Separation & Processing Strategic Isotope Production Super Heavy Element Discovery Nuclear Security Science & Technology Nuclear Systems...

131

Laser program annual report, 1979  

SciTech Connect

Volume 3 comprises three sections, beginning with Section 7 on advanced quantum electronics. Both theoretical and experimental research and development activities on advanced laser concepts in the quest for high efficiency and high repetition rate are presented. Section 8 contains the results of studies by the Energy and Military Applications group. Section 9 presents results from some of the activities of the advanced isotope separation program. (MOW)

Coleman, L.W.; Strack, J.R. (eds.)

1980-03-01T23:59:59.000Z

132

Doppler-free spectroscopy of the 1S0-3P0 optical clock transition in laser-cooled fermionic isotopes of neutral mercury  

E-Print Network (OSTI)

We have performed for the first time direct laser spectroscopy of the 1S0-3P0 optical clock transition at 265.6 nm in fermionic isotopes of neutral mercury laser-cooled in a magneto-optical trap. Spectroscopy is performed by measuring the depletion of the magneto-optical trap induced by the excitation of the long-lived 3P0 state by a probe at 265.6 nm. Measurements resolve the Doppler-free recoil doublet allowing for a determination of the transition frequency to an uncer- tainty well below the Doppler-broadened linewidth. We have performed absolute measurement of the frequency with respect to an ultra-stable reference monitored by LNE-SYRTE fountain pri- mary frequency standards using a femtosecond laser frequency comb. The measured frequency is 1128575290808 +/- 5.6 kHz in 199Hg and 1128569561140 +/- 5.3 kHz in 201Hg, more than 4 orders of magnitude better than previous indirect determinations. Owing to a low sensitivity to blackbody radiation, mercury is a promising candidate for reaching the ultimate performance of optical lattice clocks.

M. Petersen; R. Chicireanu; S. T. Dawkins; D. V. Magalhăes; C. Mandache; Y. Lecoq; A. Clairon; S. Bize

2008-07-22T23:59:59.000Z

133

Laser induced chemical reactions  

E-Print Network (OSTI)

of Basic Energy Sciences, Chemical Sciences Division of theINFRARED LASER ENHANCEMENT OF CHEMICAL REACTIONS A. B. C. D.Laser Inhibition of Chemical Reaction Effect of Isotopic

Orel, Ann E.

2010-01-01T23:59:59.000Z

134

The Separation of Phenylglycinol by a Continuous Multistage Extraction  

E-Print Network (OSTI)

, mixer settlers or centrifugal contactors for use in a plant for the reprocessing of irradiated fuel whether the intended use is uranium isotope separation or stable isotope separation are: gas centrifuge designed or prepared" for the separation of isotopes of uranium include: 5.1. Gas centrifuges

Groningen, Rijksuniversiteit

135

Cryogenic Adsorption of Hydrogen Isotopes over Nano-Structured Materials  

Science Conference Proceedings (OSTI)

Detritiation and Isotope Separation / Proceedings of the Ninth International Conference on Tritium Science and Technology (Part 2)

X. Xiao; L. K. Heung

136

Facility for Endurance Testing of Hydrophobic Isotope Exchange Catalysts  

Science Conference Proceedings (OSTI)

Detritiation and Isotope Separation / Proceedings of the Ninth International Conference on Tritium Science and Technology (Part 2)

Lidia Matei; C. Postolache; C. Tuta; S. Brad

137

Laser Enrichment LLC Early Submittal of an Environmental Report,"  

E-Print Network (OSTI)

70.21, GE-Hitachi Global Laser Enrichment LLC (GLE) is submitting an application for the construction and operation of the GLE Commercial Facility in accordance with the requirements of 10 CFR Parts 30, 40, and 70. This proposed uranium enrichment facility will utilize a laser-based isotope separation technology to enrich uranium hexafluoride up to 8%, will have a nominal capacity of up to six million separative work units, and will be located in New Hanover County, North Carolina. On January 30, 2009, the GLE Commercial Facility Environmental Report was submitted

Tammy G. Orr; Michael F. Weber

2009-01-01T23:59:59.000Z

138

Oxygen Isotopes  

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

Pages to Isotopes Data Modern Records of Carbon and Oxygen Isotopes in Atmospheric Carbon Dioxide and Carbon-13 in Methane 800,000 Deuterium Record and Shorter Records of...

139

Selective Isotope Determination of Uranium using HR-RIMS  

Science Conference Proceedings (OSTI)

The detection of lowest abundances of the ultra trace isotope {sup 236}U in environmental samples requires an efficient detection method which allows a high elemental and isotopic selectivity to suppress neighbouring isotopes of the same element and other background. High Resolution Laser Resonance Ionization Mass Spectrometry (HR-RIMS) uses the individual electron structure of each isotope to provide an outstanding element and isotope selective ionization.

Raeder, S.; Fies, S.; Wendt, K. D. A. [Institut fuer Physik, Johannes Gutenberg Universitaet Mainz, 55128 Mainz (Germany); Tomita, H. [Nagoya University (Japan)

2009-03-17T23:59:59.000Z

140

Optimisation of a multistage pulsed dye laser system  

SciTech Connect

A multistage narrow-band dye laser amplifying system with an output power of up to several kilowatts is considered as a whole. Such systems became necessary due to the development of the method of laser isotope separation (the AVLIS method). The use of the simplified model of an amplifying cell allowed us to solve analytically the equations describing the laser system and to determine optimal parameters of each stage. The dye laser system with an output power of 1 kW is optimised based on the model proposed. The accuracy of the obtained estimates was verified by a direct numerical simulation of the system based on a rigorous solution of the equations describing the interaction of radiation with the dye solution. (lasers, active media)

Vasil'ev, S V; Kuz'mina, M A; Mishin, V A [A.M. Prokhorov General Physics Institute, Russian Academy of Sciences, Moscow (Russian Federation)

2001-06-30T23:59:59.000Z

Note: This page contains sample records for the topic "laser isotope separation" 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

Definition: Isotopic Analysis | Open Energy Information  

Open Energy Info (EERE)

Analysis Analysis Jump to: navigation, search Dictionary.png Isotopic Analysis Isotopes are atoms of the same element that have different numbers of neutrons. An isotopic analysis looks at a particular isotopic element(s) in a given system, while the conditions which increase/decrease the number of neutrons are well understood and measurable.[1] View on Wikipedia Wikipedia Definition Isotope analysis is the identification of isotopic signature, the distribution of certain stable isotopes and chemical elements within chemical compounds. This can be applied to a food web to make it possible to draw direct inferences regarding diet, trophic level, and subsistence. Isotope ratios are measured using mass spectrometry, which separates the different isotopes of an element on the basis of their mass-to-charge

142

Tritium removal from contaminated water via infrared laser multiple-photon dissociation  

Science Conference Proceedings (OSTI)

Isotope separation by means of infrared-laser multiple-photon dissociation offers an efficient way to recover tritium from contaminated light or heavy water found in fission and fusion reactors. For tritium recovery from heavy water, chemical exchange of tritium into deuterated chloroform is followed by selective laser dissociation of tritiated chloroform and removal of the tritiated photoproduct, TCl. The single-step separation factor is at least 2700 and is probably greater than 5000. Here we present a description of the tritium recovery process, along with recent accomplishments in photochemical studies and engineering analysis of a recovery system.

Maienschein, J.L.; Magnotta, F.; Herman, I.P.; Aldridge, F.T.; Hsiao, P.

1983-01-01T23:59:59.000Z

143

Carbon Isotopes  

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

Atmospheric Trace Gases » Carbon Isotopes Atmospheric Trace Gases » Carbon Isotopes Carbon Isotopes Gateway Pages to Isotopes Data Modern Records of Carbon and Oxygen Isotopes in Atmospheric Carbon Dioxide and Carbon-13 in Methane 800,000 Deuterium Record and Shorter Records of Various Isotopic Species from Ice Cores Carbon-13 13C in CO Measurements from Niwot Ridge, Colorado and Montana de Oro, California (Tyler) 13C in CO2 NOAA/CMDL Flask Network (White and Vaughn) CSIRO GASLAB Flask Network (Allison, Francey, and Krummel) CSIRO in situ measurements at Cape Grim, Tasmania (Francey and Allison) Scripps Institution of Oceanography (Keeling et al.) 13C in CH4 NOAA/CMDL Flask Network (Miller and White) Northern & Southern Hemisphere Sites (Quay and Stutsman) Northern & Southern Hemisphere Sites (Stevens)

144

Battery separators  

SciTech Connect

Novel, improved battery separators carrying a plurality of polymeric ribs on at least one separator surface. The battery separators are produced by extruding a plurality of ribs in the form of molten polymeric rib providing material onto the surface of a battery separator to bond the material to the separator surface and cooling the extruded rib material to a solidified state. The molten polymeric rib providing material of this invention includes a mixture or blend of polypropylenes and an ethylene propylene diene terpolymer.

Battersby, W. R.

1984-12-25T23:59:59.000Z

145

Ionic Liquids as New Solvents for Improved Separation of ...  

A series of ionic liquids (ILs) have recently been applied as new solvents for potentially effective separation of different medical isotopes at ORNL. ...

146

Laser device  

DOE Patents (OSTI)

A laser device includes a target position, an optical component separated a distance J from the target position, and a laser energy source separated a distance H from the optical component, distance H being greater than distance J. A laser source manipulation mechanism exhibits a mechanical resolution of positioning the laser source. The mechanical resolution is less than a spatial resolution of laser energy at the target position as directed through the optical component. A vertical and a lateral index that intersect at an origin can be defined for the optical component. The manipulation mechanism can auto align laser aim through the origin during laser source motion. The laser source manipulation mechanism can include a mechanical index. The mechanical index can include a pivot point for laser source lateral motion and a reference point for laser source vertical motion. The target position can be located within an adverse environment including at least one of a high magnetic field, a vacuum system, a high pressure system, and a hazardous zone. The laser source and an electro-mechanical part of the manipulation mechanism can be located outside the adverse environment. The manipulation mechanism can include a Peaucellier linkage.

Scott, Jill R. (Idaho Falls, ID); Tremblay, Paul L. (Idaho Falls, ID)

2007-07-10T23:59:59.000Z

147

Performance Characterization of Hydrogen Isotope Exchange and Recombination Catalysts for Tritium Processing  

Science Conference Proceedings (OSTI)

Detritiation and Isotope Separation / Proceedings of the Ninth International Conference on Tritium Science and Technology (Part 2)

S. Suppiah; D. Ryland; K. Marcinkowska; H. Boniface; A. Everatt

148

Evaluation of Hydrogen Isotope Oxidation Process in an Atmospheric Pressure Plasma  

Science Conference Proceedings (OSTI)

Detritiation and Isotope Separation / Proceedings of the Ninth International Conference on Tritium Science and Technology (Part 2)

K. Akahane; N. Ezumi; Y. Uesugi; Y. Tanaka; M. Tanaka; K. Nishimura

149

Battery separators  

Science Conference Proceedings (OSTI)

A novel, improved battery separator and process for making the separator. Essentially, the separator carries a plurality of polymeric ribs bonded to at least one surface and the ribs have alternating elevated segments of uniform maxiumum heights and depressed segments along the length of the ribs.

Le Bayon, R.; Faucon, R.; Legrix, J.

1984-11-13T23:59:59.000Z

150

BNL | Nd:YAG Laser  

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

Nd:YAG Laser The Nd:YAG laser is located in a class 1000 clean room (the YAG Room) near the electron gun end of the ATF accelerator. The clean area also includes a separate laser...

151

Stable Isotope Enrichment Capabilities at ORNL  

SciTech Connect

The Oak Ridge National Laboratory (ORNL) and the US Department of Energy Nuclear Physics Program have built a high-resolution Electromagnetic Isotope Separator (EMIS) as a prototype for reestablishing a US based enrichment capability for stable isotopes. ORNL has over 60 years of experience providing enriched stable isotopes and related technical services to the international accelerator target community, as well as medical, research, industrial, national security, and other communities. ORNL is investigating the combined use of electromagnetic and gas centrifuge isotope separation technologies to provide research quantities (milligram to several kilograms) of enriched stable isotopes. In preparation for implementing a larger scale production facility, a 10 mA high-resolution EMIS prototype has been built and tested. Initial testing of the device has simultaneously collected greater than 98% enriched samples of all the molybdenum isotopes from natural abundance feedstock.

Egle, Brian [ORNL; Aaron, W Scott [ORNL; Hart, Kevin J [ORNL

2013-01-01T23:59:59.000Z

152

AVLIS enrichment of medical isotopes  

SciTech Connect

Under the Sponsorship of the United states Enrichment Corporation (USEC), we are currently investigating the large scale separation of several isotopes of medical interest using atomic vapor isotope separation (AVLIS). This work includes analysis and experiments in the enrichment of thallium 203 as a precursor to the production of thallium 201 used in cardiac imaging following heart attacks, on the stripping of strontium 84 from natural strontium as precursor to the production of strontium 89, and on the stripping of lead 210 from lead used in integrated circuits to reduce the number of alpha particle induced logic errors.

Haynam, C.A.; Scheibner, K.F.; Stern, R.C.; Worden, E.F. [Lawrence Livermore National Laboratory, CA (United States)

1996-12-31T23:59:59.000Z

153

Method and Apparatus for separation of heavy and tritiated water  

DOE Patents (OSTI)

An object of the present invention is to provide a method for separating and recovering hydrogen isotopes that avoids the disadvantages of the prior art, is more simple, and allows for continuous hydrogen isotope separation and recovery. The disclosed invention does not require the use of isotope exchange reaction catalysts and/or hydrogen sulfide gas. The present invention achieves the advantages of the thermal diffusion and the chemical exchange processes. The disclosed invention provides a method for separating and recovering hydrogen isotopes from a fluid containing the hydrogen isotopes by providing counter-current cold and hot streams of the fluid containing the hydrogen isotopes separated by a proton exchange membrane made of thermally insulating and chemically transparent material that allows exchange of heavy and light hydrogen isotopes there through. The heavier isotopes migrate to the cold stream producing a deuterium and tritium-enriched fluid, while lighter isotopes migrate to the hot stream producing a lighter isotope-enriched fluid. The heavy and light isotopes are withdrawn from the cold and hot streams respectively. According to the present invention, the fluid is water or hydrogen gas, and the desired hydrogen isotope species are deuterium and/or tritium. Further, according to the present invention, the streams of said high and low temperature fluids are interconnected at their respective top and bottom ends forming a continuous loop, and a feed stream is provided at an intermediate portion of either hot or cold stream to feed the process.

Lee, Myung, W.

2000-02-28T23:59:59.000Z

154

Short wavelength laser  

DOE Patents (OSTI)

A short wavelength laser is provided that is driven by conventional-laser pulses. A multiplicity of panels, mounted on substrates, are supported in two separated and alternately staggered facing and parallel arrays disposed along an approximately linear path. When the panels are illuminated by the conventional-laser pulses, single pass EUV or soft x-ray laser pulses are produced.

Hagelstein, P.L.

1984-06-25T23:59:59.000Z

155

A Microdrop Generator for the Calibration of a Water Vapor Isotope Ratio Spectrometer  

Science Conference Proceedings (OSTI)

A microdrop generator is described that produces water vapor with a known isotopic composition and volume mixing ratio for the calibration of a near-infrared diode laser water isotope ratio spectrometer. The spectrometer is designed to measure in ...

Rosario Q. Iannone; Daniele Romanini; Samir Kassi; Harro A. J. Meijer; Erik R. Th Kerstel

2009-07-01T23:59:59.000Z

156

from Isotope Production Facility  

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

Cancer-fighting treatment gets boost from Isotope Production Facility April 13, 2012 Isotope Production Facility produces cancer-fighting actinium - 2 - 2:32 Isotope cancer...

157

Modeling of the Process of Three-Isotope (H, D, T) Exchange Between Hydrogen Gas and Water Vapour on Pt-SDBC Catalyst over a Wide Range of Deuterium Concentration  

Science Conference Proceedings (OSTI)

Technical Paper / Tritium Science and Technology - Tritium Science and Technology - Detritiation, Purification, and Isotope Separation

O. A. Fedorchenko; I. A. Alekseev; A. S. Tchijov; V. V. Uborsky

158

Char separator  

DOE Patents (OSTI)

Particulates removed from the flue gases produced in a fluidized-bed furnace are separated into high-and low-density portions. The low-density portion is predominantly char, and it is returned to the furnace or burned in a separate carbon burnup cell. The high-density portion, which is predominantly limestone products and ash, is discarded or reprocessed. According to another version, the material drained from the bed is separated, the resulting high-and low-density portions being treated in a manner similar to that in which the flue-gas particulates are treated.

Matthews, Francis T. (Poquonock, CT)

1979-01-01T23:59:59.000Z

159

CENTRIFUGAL SEPARATORS  

DOE Patents (OSTI)

A centrifugal separator is described for separating gaseous mixtures where the temperature gradients both longitudinally and radially of the centrifuge may be controlled effectively to produce a maximum separation of the process gases flowing through. Tbe invention provides for the balancing of increases and decreases in temperature in various zones of the centrifuge chamber as the result of compression and expansions respectively, of process gases and may be employed effectively both to neutralize harmful temperature gradients and to utilize beneficial temperaturc gradients within the centrifuge.

Skarstrom, C.

1959-03-10T23:59:59.000Z

160

Specification of optical components for a high average-power laser environment  

Science Conference Proceedings (OSTI)

Optical component specifications for the high-average-power lasers and transport system used in the Atomic Vapor Laser Isotope Separation (AVLIS) plant must address demanding system performance requirements. The need for high performance optics has to be balanced against the practical desire to reduce the supply risks of cost and schedule. This is addressed in optical system design, careful planning with the optical industry, demonstration of plant quality parts, qualification of optical suppliers and processes, comprehensive procedures for evaluation and test, and a plan for corrective action.

Taylor, J.R.; Chow, R.; Rinmdahl, K.A.; Willis, J.B.; Wong, J.N.

1997-06-25T23:59:59.000Z

Note: This page contains sample records for the topic "laser isotope separation" 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

Low-energy Coulomb excitation of neutron-rich zinc isotopes  

E-Print Network (OSTI)

At the radioactive ion beam facility REX-ISOLDE, neutron-rich zinc isotopes were investigated using low-energy Coulomb excitation. These experiments have resulted in B(E2,20) values in 74-80Zn, B(E2,42) values in 74,76Zn and the determination of the energy of the first excited 2 states in 78,80Zn. The zinc isotopes were produced by high-energy proton- (A=74,76,80) and neutron- (A=78) induced fission of 238U, combined with selective laser ionization and mass separation. The isobaric beam was postaccelerated by the REX linear accelerator and Coulomb excitation was induced on a thin secondary target, which was surrounded by the MINIBALL germanium detector array. In this work, it is shown how the selective laser ionization can be used to deal with the considerable isobaric beam contamination and how a reliable normalization of the experiment can be achieved. The results for zinc isotopes and the N=50 isotones are compared to collective model predictions and state-of-the-art large-scale shell-model calculations, i...

Van de Walle, J; Behrens, T; Bildstein, V; Blazhev, A; Cederkäll, J; Clément, E; Cocolios, T E; Davinson, T; Delahaye, P; Eberth, J; Ekström, A; Fedorov, D V; Fedosseev, V; Fraile, L M; Franchoo, S; Gernhäuser, R; Georgiev, G; Habs, D; Heyde, K; Huber, G; Huyse, M; Ibrahim, F; Ivanov, O; Iwanicki, J; Jolie, J; Kester, O; Köster, U; Kröll, T; Krücken, R; Lauer, M; Lisetskiy, A F; Lutter, R; Marsh, B A; Mayet, P; Niedermaier, O; Pantea, M; Raabe, R; Reiter, P; Sawicka, M; Scheit, H; Schrieder, G; Schwalm, D; Seliverstov, M D; Sieber, T; Sletten, G; Smirnova, N; Stanoiu, M; Stefanescu, I; Thomas, J C; Valiente-Dobón, J J; Van Duppen, P; Verney, D; Voulot, D; Warr, N; Weisshaar, D; Wenander, F; Wolf, B H; Zielinska, M

2009-01-01T23:59:59.000Z

162

Method and apparatus for tritiated water separation  

DOE Patents (OSTI)

The present invention is a membrane method and apparatus for separating isotopic water constituents from light water. The method involves providing a supported membrane of an aromatic polyphosphazene and pressurizing the water on one side of the membrane thereby forcing the light water through the supported membrane while isotopic water constituents are retained or vice versa. The apparatus of the present invention includes an aromatic polyphosphazene placed on a porous support and means for pressurizing water through the membrane while certain isotopic water constituents are retained.

Nelson, David A. (Richland, WA); Duncan, James B. (Kennewick, WA); Jensen, George A. (Richland, WA)

1995-01-01T23:59:59.000Z

163

System and method for high precision isotope ratio destructive analysis  

DOE Patents (OSTI)

A system and process are disclosed that provide high accuracy and high precision destructive analysis measurements for isotope ratio determination of relative isotope abundance distributions in liquids, solids, and particulate samples. The invention utilizes a collinear probe beam to interrogate a laser ablated plume. This invention provides enhanced single-shot detection sensitivity approaching the femtogram range, and isotope ratios that can be determined at approximately 1% or better precision and accuracy (relative standard deviation).

Bushaw, Bruce A; Anheier, Norman C; Phillips, Jon R

2013-07-02T23:59:59.000Z

164

Gas separating  

DOE Patents (OSTI)

Feed gas is directed tangentially along the non-skin surface of gas separation membrane modules comprising a cylindrical bundle of parallel contiguous hollow fibers supported to allow feed gas to flow from an inlet at one end of a cylindrical housing through the bores of the bundled fibers to an outlet at the other end while a component of the feed gas permeates through the fibers, each having the skin side on the outside, through a permeate outlet in the cylindrical casing. 3 figs.

Gollan, A.

1988-03-29T23:59:59.000Z

165

Separation processes using expulsion from dilute supercritical solutions  

DOE Patents (OSTI)

This invention relates to separation processes and particularly to isotope separation processes performed near the critical point of solvents for separation of solutes therefrom, and was developed pursuant to a contract with 5 the United States Department of Energy, contract number DE-AC05-84OR21400, and funded under WPF number ERKCT07.

Cochran, H.D. Jr.

1991-01-01T23:59:59.000Z

166

Separation processes using expulsion from dilute supercritical solutions  

DOE Patents (OSTI)

This invention relates to separation processes and particularly to isotope separation processes performed near the critical point of solvents for separation of solutes therefrom, and was developed pursuant to a contract with 5 the United States Department of Energy, contract number DE-AC05-84OR21400, and funded under WPF number ERKCT07.

Cochran, H.D. Jr.

1991-12-31T23:59:59.000Z

167

Glossary Term - Isotope  

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

Helios Previous Term (Helios) Glossary Main Index Next Term (Joule) Joule Isotope The Three Isotopes of Hydrogen - Protium, Deuterium and Tritium Atoms that have the same number of...

168

Measurement of Pressure Drop and HETP in Columns Packed with Different Hydrophobic Catalysts for Tritium Isotopic Exchange Between Water and Hydrogen  

Science Conference Proceedings (OSTI)

Isotope Separation / Proceedings of the Sixth International Conference on Tritium Science and Technology Tsukuba, Japan November 12-16, 2001

A. Perevezentsev; A. Bell; B.M. Andreev; E.P. Magomedbekov; Yu.S. Pak; M.B. Rozenkevich; Yu.A. Sakharovskii

169

Particle separation  

DOE Patents (OSTI)

Embodiments of a method for selecting particles, such as based on their morphology, is disclosed. In a particular example, the particles are charged and acquire different amounts of charge, or have different charge distributions, based on their morphology. The particles are then sorted based on their flow properties. In a specific example, the particles are sorted using a differential mobility analyzer, which sorts particles, at least in part, based on their electrical mobility. Given a population of particles with similar electrical mobilities, the disclosed process can be used to sort particles based on the net charge carried by the particle, and thus, given the relationship between charge and morphology, separate the particles based on their morphology.

Moosmuller, Hans (Reno, NV); Chakrabarty, Rajan K. (Reno, NV); Arnott, W. Patrick (Reno, NV)

2011-04-26T23:59:59.000Z

170

Separation processes using expulsion from dilute supercritical solutions  

DOE Patents (OSTI)

A process for separating isotopes as well as other mixtures by utilizing the behavior of dilute repulsive or weakly attractive elements of the mixtures as the critical point of the solvent is approached.

Cochran, Jr., Henry D. (Oak Ridge, TN)

1993-01-01T23:59:59.000Z

171

Separation processes using expulsion from dilute supercritical solutions  

DOE Patents (OSTI)

A process is described for separating isotopes as well as other mixtures by utilizing the behavior of dilute repulsive or weakly attractive elements of the mixtures as the critical point of the solvent is approached.

Cochran, H.D. Jr.

1993-04-20T23:59:59.000Z

172

Stable isotope studies  

SciTech Connect

The research has been in four general areas: (1) correlation of isotope effects with molecular forces and molecular structures, (2) correlation of zero-point energy and its isotope effects with molecular structure and molecular forces, (3) vapor pressure isotope effects, and (4) fractionation of stable isotopes. 73 refs, 38 figs, 29 tabs.

Ishida, T.

1992-01-01T23:59:59.000Z

173

Separation Processes, Second Edition  

E-Print Network (OSTI)

process for uranium-isotope enrichment. distillation columnenrichment they can provide, for the recovery of 235U from natural uranium

King, C. Judson

1980-01-01T23:59:59.000Z

174

Isotopes: Isotope Production, Medical IsotopesOffice of Science...  

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

Managers Put a short description of the graphic or its primary message here Isotope Production and Applications The Los Alamos National Laboratory has produced radioactive...

175

Method and apparatus for noble gas atom detection with isotopic selectivity  

DOE Patents (OSTI)

Apparatus and methods of operation are described for determining, with isotopic selectivity, the number of noble gas atoms in a sample. The analysis is conducted within an evacuated chamber which can be isolated by a valve from a vacuum pumping system capable of producing a pressure of 10.sup.-8 Torr. Provision is made to pass pulses of laser beams through the chamber, these pulses having wavelengths appropriate for the resonance ionization of atoms of the noble gas under analysis. A mass filter within the chamber selects ions of a specific isotope of the noble gas, and means are provided to accelerate these selected ions sufficiently for implantation into a target. Specific types of targets are discussed. An electron measuring device produces a signal relatable to the number of ions implanted into the target and thus to the number of atoms of the selected isotope of the noble gas removed from the gas sample. The measurement can be continued until a substantial fraction, or all, of the atoms in the sample have been counted. Furthermore, additional embodiments of the apparatus are described for bunching the atoms of a noble gas for more rapid analysis, and for changing the target for repetitive cycling of the gas in the chamber. The number of repetitions of the cyclic steps depend upon the concentration of the isotope of interest, the separative efficiency of the mass filter, etc. The cycles are continued until a desired selectivity is achieved. Also described are components and a method of operation for a pre-enrichment operation for use when an introduction of a total sample would elevate the pressure within the chamber to levels in excess of those for operation of the mass filter, specifically a quadrupole mass filter. Specific examples of three noble gas isotope analyses are described.

Hurst, G. Samuel (Oak Ridge, TN); Payne, Marvin G. (Harriman, TN); Chen, Chung-Hsuan (Knoxville, TN); Parks, James E. (Oak Ridge, TN)

1984-01-01T23:59:59.000Z

176

Method for sequential injection of liquid samples for radioisotope separations  

DOE Patents (OSTI)

The present invention is a method of separating a short-lived daughter isotope from a longer lived parent isotope, with recovery of the parent isotope for further use. Using a system with a bi-directional pump and one or more valves, a solution of the parent isotope is processed to generate two separate solutions, one of which contains the daughter isotope, from which the parent has been removed with a high decontamination factor, and the other solution contains the recovered parent isotope. The process can be repeated on this solution of the parent isotope. The system with the fluid drive and one or more valves is controlled by a program on a microprocessor executing a series of steps to accomplish the operation. In one approach, the cow solution is passed through a separation medium that selectively retains the desired daughter isotope, while the parent isotope and the matrix pass through the medium. After washing this medium, the daughter is released from the separation medium using another solution. With the automated generator of the present invention, all solution handling steps necessary to perform a daughter/parent radionuclide separation, e.g. Bi-213 from Ac-225 "cow" solution, are performed in a consistent, enclosed, and remotely operated format. Operator exposure and spread of contamination are greatly minimized compared to the manual generator procedure described in U.S. patent application Ser. No. 08/789,973, now U.S. Pat. No. 5,749,042, herein incorporated by reference. Using 16 mCi of Ac-225 there was no detectable external contamination of the instrument components.

Egorov, Oleg B. (Richland, WA); Grate, Jay W. (West Richland, WA); Bray, Lane A. (Richland, WA)

2000-01-01T23:59:59.000Z

177

Isotope Enrichment Calculator  

Science Conference Proceedings (OSTI)

... incremental isotopic percentages which are compared with an input experimentally derived profile. The theoretical profile of 15 N percentage which ...

2012-10-09T23:59:59.000Z

178

Stable Isotope Enrichment by Thermal Diffusion, Chemical Exchange, and Distillation  

SciTech Connect

Applications of stable isotopes in medicine are becoming more widespread. This has resulted from the increased availability and reduced cost of these isotopes and the improved reliability and sensitivity of detection techniques such as carbon-13 nuclear magnetic resonance. Isotopes are used in compounds labeled with either the stable isotope itself, such as carbon-13 and oxygen-18, or with the radioactive isotope that can be produced by irradiating the stable isotope, such as the irradiation of xenon-124 to produce iodine-125. As the demand for stable isotopes increases, larger scale production facilities will be justifiable. The increased size of production facilities should result in yet lower unit selling prices. A large number of methods has been suggested for the separation of stable isotopes. This paper concerns itself with four methods which have proven extremely useful for the separation of the isotopes of low and medium atomic weight elements. The four processes discussed are gas phase thermal diffusion, liquid phase thermal diffusion, chemical exchange, and distillation.

Schwind, Dr. Roger A.; Rutherford, Dr. William M.

1973-03-01T23:59:59.000Z

179

Mathematical models for D2-DTO isotopic exchange process of detritiation systems  

Science Conference Proceedings (OSTI)

The present work has the purpose to determine the flow behavior of both phases, gaseous and liquid, of the hydrogen isotopes in order to obtain a better separation factor between hydrogen and water, ?D/T, in the D2-DTO large ... Keywords: isotopic exchange column, separation factor, tritiated heavy water

Sorin Gherghinescu

2010-06-01T23:59:59.000Z

180

Tritium removal and separation technology developments  

Science Conference Proceedings (OSTI)

Recent increased interest from regulators and the public has led more organizations to consider the environmental impact and safety considerations of tritium handling. Examples include the significance of the tritium isotope separation system on ITER licensing, remediation of ground water from power utilities and government facilities and concerns of high tritium concentrations within operational CANDU reactors. GE Healthcare, formerly Amersham pic, has been producing tritium-labelled chemicals since the late 1940's. GE's manufacturing site located near Cardiff, UK has installed a tritium waste treatment and enrichment facility to radically reduce tritium discharges to the environment. This facility employs a continuous processing plant that recovers tritium from a complex mixture of tritiated organic and aqueous waste compounds. Two isotope separation techniques are used to achieve a final pure tritium product, which is used in the manufacturing of labelled compounds. Building upon this experience, together with Special Separations Applications Inc. (SSAI), GE has developed a large-scale diffusion-based isotope separation process as an alternative to conventional cryogenic distillation. Having a tritium inventory an order of magnitude lower than conventional cryogenic distillation, this process is attractive for heavy water detritiation, applicable to single and multi-unit CANDU reactors and research reactors as well as fusion applications. Additionally, the new process has advantages of being cryogen-free, less complex, simple to operate and having improved conventional and radiological safety. (authors)

Bonnett, I. [General Electric, Hitachi Nuclear Energy Canada Inc., 1160 Monaghan Rd, Peterborough, ON K9J 7B5 (Canada); Busigin, A. [Special Separations Applications, Inc., 55 Water Street East, Brockville, ON K6V 1A3 (Canada); Shapiro, A. [General Electric GE, Global Research Center, 1 Research Circle, Niskayuna, NY 12309 (United States)

2008-07-15T23:59:59.000Z

Note: This page contains sample records for the topic "laser isotope separation" 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

Isotopically controlled semiconductors  

SciTech Connect

Semiconductor bulk crystals and multilayer structures with controlled isotopic composition have attracted much scientific and technical interest in the past few years. Isotopic composition affects a large number of physical properties, including phonon energies and lifetimes, bandgaps, the thermal conductivity and expansion coefficient and spin-related effects. Isotope superlattices are ideal media for self-diffusion studies. In combination with neutron transmutation doping, isotope control offers a novel approach to metal-insulator transition studies. Spintronics, quantum computing and nanoparticle science are emerging fields using isotope control.

Haller, Eugene E.

2001-12-21T23:59:59.000Z

182

ARM - Measurement - Isotope ratio  

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

govMeasurementsIsotope ratio govMeasurementsIsotope ratio ARM Data Discovery Browse Data Comments? We would love to hear from you! Send us a note below or call us at 1-888-ARM-DATA. Send Measurement : Isotope ratio Ratio of stable isotope concentrations. Categories Atmospheric Carbon, Atmospheric State Instruments The above measurement is considered scientifically relevant for the following instruments. Refer to the datastream (netcdf) file headers of each instrument for a list of all available measurements, including those recorded for diagnostic or quality assurance purposes. ARM Instruments FLASK : Flask Samplers for Carbon Cycle Gases and Isotopes Field Campaign Instruments FLASK : Flask Samplers for Carbon Cycle Gases and Isotopes Datastreams FLASK : Flask Samplers for Carbon Cycle Gases and Isotopes

183

Packed bed reactor for photochemical .sup.196 Hg isotope separation  

DOE Patents (OSTI)

Straight tubes and randomly oriented pieces of tubing having been employed in a photochemical mercury enrichment reactor and have been found to improve the enrichment factor (E) and utilization (U) compared to a non-packed reactor. One preferred embodiment of this system uses a moving bed (via gravity) for random packing.

Grossman, Mark W. (Belmont, MA); Speer, Richard (Reading, MA)

1992-01-01T23:59:59.000Z

184

AMMONIA DISTILLATION FOR DEUTERIUM SEPARATION  

SciTech Connect

The relative volatility or separation factor for deuterium enrichment in ammonia distillation was measured at several pressures and deuterium concentrations. The knowledge of this ingormation is very helpful in predicting costs of heawy water production by the ammonia distillation process. It hss been stated by others, that the ammonia distillation process of heawy water production would be competitive with other developed methods only if the actusl separation factor was at least 1.062 at low deuterium concentration. Ungortunately, the measurements do not indicate that the separation factor at low deuterium composition differs greatly from the vapor pressure pre diction ( alpha = 1.042). Deutero-ammonia was synthesized by isotopic exchange between natural ammonia and heavy water. Equilibrium determinations were made using an Othmer still, modified for low temperature operation, and a concentric tube fractionating column. The arnmonia samples were analyzed for deuterium content by converting them to water by flow torough hot copper oxide, followed by a differential density determination using the falling drop method. ( auth)

Petersen, G.T.; Benedict, M.

1960-05-16T23:59:59.000Z

185

HYDROGEN ISOTOPE TARGETS  

DOE Patents (OSTI)

The design of targets for use in the investigation of nuclear reactions of hydrogen isotopes by bombardment with accelerated particles is described. The target con struction eomprises a backing disc of a metal selected from the group consisting of molybdenunn and tungsten, a eoating of condensed titaniunn on the dise, and a hydrogen isotope selected from the group consisting of deuterium and tritium absorbed in the coatiag. The proeess for preparing these hydrogen isotope targets is described.

Ashley, R.W.

1958-08-12T23:59:59.000Z

186

Discovery of the Mercury Isotopes  

E-Print Network (OSTI)

Forty mercury isotopes have so far been observed; the discovery of these isotopes is discussed. For each isotope a brief summary of the first refereed publication, including the production and identification method, is presented.

D. Meierfrankenfeld; M. Thoennessen

2009-12-01T23:59:59.000Z

187

Laser Ignition  

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

Ignition Laser Ignition A first excitation laser or other excitation light source is used in tandem with an ignitor laser to provide a compact, durable, engine deployable fuel...

188

Fuel Cycle and Isotopes Division  

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

Divisions Fuel Cycle and Isotopes Division Jeffrey Binder, Division Director Jeffrey Binder, Division Director The Fuel Cycle and Isotopes Division (FCID) of the Nuclear Science...

189

Isotopic Analysis | Open Energy Information  

Open Energy Info (EERE)

Structural: Hydrological: Source of fluids, circulation, andor mixing. Thermal: Heat source and general reservoir temperatures Dictionary.png Isotopic Analysis: Isotopes...

190

Tunable Diode-Laser Absorption Spectroscopy for Trace-Gas Measurements with High Sensitivity and Low Drift.  

E-Print Network (OSTI)

??This book discusses the mechanical and opto-electronic design of laser spectrometers for measuring two very important atmospheric gases, namely water vapor and its isotopic ratios,… (more)

Dyroff, Christoph

2009-01-01T23:59:59.000Z

191

Apparatus and method for monitoring of gas having stable isotopes  

DOE Patents (OSTI)

Gas having stable isotopes is monitored continuously by using a system that sends a modulated laser beam to the gas and collects and transmits the light not absorbed by the gas to a detector. Gas from geological storage, or from the atmosphere can be monitored continuously without collecting samples and transporting them to a lab.

Clegg, Samuel M; Fessenden-Rahn, Julianna E

2013-03-05T23:59:59.000Z

192

Isotope and Nuclear Chemistry Division annual report, FY 1983  

Science Conference Proceedings (OSTI)

This report describes progress in the major research and development programs carried out in FY 1983 by the Isotope and Nuclear Chemistry Division. It covers radiochemical diagnostics of weapons tests; weapons radiochemical diagnostics research and development; other unclassified weapons research; stable and radioactive isotope production, separation, and applications (including biomedical applications); element and isotope transport and fixation; actinide and transition metal chemistry; structural chemistry, spectroscopy, and applications; nuclear structure and reactions; irradiation facilities; advanced analytical techniques; development and applications; atmospheric chemistry and transport; and earth and planetary processes.

Heiken, J.H.; Lindberg, H.A. (eds.)

1984-05-01T23:59:59.000Z

193

Method for isotopic analysis of chlorinated organic compounds  

DOE Patents (OSTI)

The present invention provides a method for preparing a VOC sample for carbon and chlorine isotope ratio analysis by mass spectrometer. A VOC sample is placed in a combustion tube and reacted with CuO to form CO.sub.2 and CuCl. The CO.sub.2 is then extracted and analyzed for the carbon isotope ratio. The CuCl is separated from the excess CuO and reacted with CH.sub.3 I to form CH.sub.3 Cl, extracted and analyzed for chlorine isotope ratio.

Holt, Ben D. (Hindsdale, IL); Sturchio, Neil C. (Oswego, IL)

1999-01-01T23:59:59.000Z

194

Determination of Actinide Isotope Ratios Using Glow Discharge Optogalvanic Spectroscopy  

SciTech Connect

Diode-laser excited optogalvanic spectroscopy (OGS) of a glow discharge has been utilized to measure U-235/U-235 + U-238 isotope ratios. This ``optical mass spectrometric`` measurement has been demonstrated for a number of samples including uranium oxide, fluoride, and metal. Various diode-laser accessible atomic transitions in the 775 to 835 nm region have been evaluated; these transitions were chosen by considering OGS sensitivity and isotope shift. Using the 831.84 nm uranium line, for example, it was possible to measure the U-235/U-235 + U-238 isotope ratio (0.0026) of depleted uranium samples. A prototypical field instrument to make these measurements has been assembled and demonstrated. A U-236 spectral line was identified in a sample of enriched uranium, and an abundance sensitivity was measured.

Young, J.P.; Shaw, R.W.; Barshick, C.M.; Ramsey, J.M.

1997-08-01T23:59:59.000Z

195

Laser Program annual report 1984  

Science Conference Proceedings (OSTI)

The Laser Program Annual Report is part of the continuing series of reports documenting the progress of the unclassified Laser Fusion Program at the Lawrence Livermore National Laboratory (LLNL). As in previous years, the report is organized programmatically. The first section is an overview of the basic goals and directions of the LLNL Inertial Confinement Fusion (ICF) Program, and highlights the year's important accomplishments. Sections 2 through 7 provide the detailed information on the various program elements: Laser Systems and Operations, Target Design, Target Fabrication, Laser Experiments and Advanced Diagnostics, Advanced Laser Development, and Applications of Inertial Confinement Fusion. Individual sections will be indexed separately. 589 refs., 333 figs., 25 tabs.

Rufer, M.L.; Murphy, P.W. (eds.)

1985-06-01T23:59:59.000Z

196

Isotope GeochemistryIsotope Geochemistry Isotopes do not fractionate during partial  

E-Print Network (OSTI)

/204Pb, 207Pb/204Pb, due to U and Th decay The isotope geology of PbThe isotope geology of Pb #12;The isotope geology of PbThe isotope geology of Pb µ = 238U/204Pb Primeval lead (Isotope ratios of Pb tT t eea Pb Pb -µ+= 30.90 204 206 == a Pb Pb i 29.100 204 207 == b Pb Pb i #12;The isotope geology

Siebel, Wolfgang

197

Isotopically controlled semiconductors  

SciTech Connect

The following article is an edited transcript based on the Turnbull Lecture given by Eugene E. Haller at the 2005 Materials Research Society Fall Meeting in Boston on November 29, 2005. The David Turnbull Lectureship is awarded to recognize the career of a scientist who has made outstanding contributions to understanding materials phenomena and properties through research, writing, and lecturing, as exemplified by the life work of David Turnbull. Haller was named the 2005 David Turnbull Lecturer for his 'pioneering achievements and leadership in establishing the field of isotopically engineered semiconductors; for outstanding contributions to materials growth, doping and diffusion; and for excellence in lecturing, writing, and fostering international collaborations'. The scientific interest, increased availability, and technological promise of highly enriched isotopes have led to a sharp rise in the number of experimental and theoretical studies with isotopically controlled semiconductor crystals. This article reviews results obtained with isotopically controlled semiconductor bulk and thin-film heterostructures. Isotopic composition affects several properties such as phonon energies, band structure, and lattice constant in subtle, but, for their physical understanding, significant ways. Large isotope-related effects are observed for thermal conductivity in local vibrational modes of impurities and after neutron transmutation doping. Spectacularly sharp photoluminescence lines have been observed in ultrapure, isotopically enriched silicon crystals. Isotope multilayer structures are especially well suited for simultaneous self- and dopant-diffusion studies. The absence of any chemical, mechanical, or electrical driving forces makes possible the study of an ideal random-walk problem. Isotopically controlled semiconductors may find applications in quantum computing, nanoscience, and spintronics.

Haller, Eugene E.

2006-06-19T23:59:59.000Z

198

Battery separator material  

SciTech Connect

A novel, improved battery separator material particularly adaptable for use in maintenance free batteries. The battery separator material includes a diatomaceous earth filler, an acrylate copolymer binder and a combination of fibers comprising polyolefin, polyester and glass fibers.

Bodendorf, W. J.

1985-07-16T23:59:59.000Z

199

Actinide separations conference  

Science Conference Proceedings (OSTI)

This report contains the abstracts for 55 presentations given at the fourteenth annual Actinide Separations Conference. (JDL)

Not Available

1990-01-01T23:59:59.000Z

200

Isotope production and distribution Programs Fiscal Year (FY) 1995 Financial Statement Audit (ER-FC-96-01)  

SciTech Connect

The charter of the Department of Energy (DOE) Isotope Production and Distribution Program (Isotope Program) covers the production and sale of radioactive and stable isotopes, associated byproducts, surplus materials such as lithium and deuterium, and related isotope services. Services provided include, but are not limited to, irradiation services, target preparation and processing, source encapsulation and other special preparations, analyses, chemical separations, and leasing of stable isotopes for research purposes. Isotope Program products and services are sold worldwide for use in a wide variety of research, development, biomedical, and industrial applications. The Isotope Program reports to the Director of the Office of Nuclear Energy, Science and Technology. The Isotope Program operates under a revolving fund, as established by the Fiscal Year 1990 Energy and Water Appropriations Act (Public Law 101-101). The Fiscal Year 1995 Appropriations Act (Public Law 103-316) modified predecessor acts to allow prices charged for Isotope Program products and services to be based on production costs, market value, the needs of the research community, and other factors. Prices set for small-volume, high-cost isotopes that are needed for research may not achieve full-cost recovery. Isotope Program costs are financed by revenues from the sale of isotopes and associated services and through payments from the isotope support decision unit, which was established in the DOE fiscal year 1995 Energy, Supply, Research, and Development appropriation. The isotope decision unit finances the production and processing of unprofitable isotopes that are vital to the national interest.

1996-02-12T23:59:59.000Z

Note: This page contains sample records for the topic "laser isotope separation" 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

Raman spectroscopic and mass spectrometric investigations of the hydrogen isotopes and isotopically labelled methane  

Science Conference Proceedings (OSTI)

Suitable analytical methods must be tested and developed for monitoring the individual process steps within the fuel cycle of a fusion reactor and for tritium accountability. The utility of laser-Raman spectroscopy accompanied by mass spectrometry with an Omegatron was investigated using the analysis of all hydrogen isotopes and isotopically labeled methanes as an example. The Omegatron is useful for analyzing all hydrogen isotopes mixed with the stable helium isotopes. The application of this mass spectrometer were demonstrated by analyzing mixtures of deuterated methanes. In addition, it was employed to study the radiochemical Witzbach exchange reaction between tritium and methanes. A laser-Raman spectrometer was designed for analysis of tritium-containing gases and was built from individual components. A tritium-compatible, metal-sealed Raman cuvette having windows with good optical properties and additional means for measuring the stray light was first used successfully in this work. The Raman spectra of the hydrogen isotopes were acquired in the pure rotation mode and in the rotation-vibration mode and were used for on. The deuterated methanes were measured by Raman spectroscopy, the wavenumbers determined were assigned to the corresponding vibrations, and the wavenumbers for the rotational fine-structure were summarized in tables. The fundamental Vibrations of the deuterated methanes produced Witzbach reactions were detected and assigned. The fundamental vibrations of the molecules were obtained with Raman spectroscopy for the first time in this work. The @-Raman spectrometer assembled is well suited for the analysis of tritium- containing gases and is practical in combination with mass spectrometry using an Omegatron, for studying gases used in fusion.

Jewett, J.R., Fluor Daniel Hanford

1997-02-24T23:59:59.000Z

202

Unattended Monitoring of HEU Production in Gaseous Centrifuge Enrichment Plants using Automated Aerosol Collection and Laser-based Enrichment Assay  

Science Conference Proceedings (OSTI)

Nuclear power is enjoying rapid growth as government energy policies and public demand shift toward low carbon energy production. Pivotal to the global nuclear power renaissance is the development and deployment of robust safeguards instrumentation that allows the limited resources of the IAEA to keep pace with the expansion of the nuclear fuel cycle. Undeclared production of highly enriched uranium (HEU) remains a primary proliferation concern for modern gaseous centrifuge enrichment plants (GCEPs), due to their massive separative work unit (SWU) processing power and comparably short cascade equilibrium timescale. The Pacific Northwest National Laboratory is developing an unattended safeguards instrument, combining continuous aerosol particulate collection with uranium isotope assay, to provide timely detection of HEU production within a GCEP. This approach is based on laser vaporization of aerosol particulates, followed by laser spectroscopy to characterize the uranium enrichment level. Our prior investigation demonstrated single-shot detection sensitivity approaching the femtogram range and relative isotope ratio uncertainty better than 10% using gadolinium as a surrogate for uranium. In this paper we present measurement results on standard samples containing traces of depleted, natural, and low enriched uranium, as well as measurements on aerodynamic size uranium particles mixed in background materials (e.g., dust, minerals, soils). Improvements and optimizations in the detection electronics, signal timing, calibration, and laser alignment have lead to significant improvements in detection sensitivity and enrichment accuracy, contributing to an overall reduction in the false alarm probability. The sample substrate media was also found to play a significant role in facilitating laser-induced vaporization and the production of energetic plasma conditions, resulting in ablation optimization and further improvements in the isotope abundance sensitivity.

Anheier, Norman C.; Bushaw, Bruce A.

2010-08-11T23:59:59.000Z

203

Strategic Isotope Production | ornl.gov  

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

Strategic Isotope Production SHARE Strategic Isotope Production ORNL's unique facilities at the High Flux Isotope Reactor (HFIR), Radiochemical Engineering Development Center...

204

Isotopes as Environmental Tracers in Archived Biological ...  

Science Conference Proceedings (OSTI)

... Tissue Archival and Monitoring Program (STAMP ... and isotopes) and carbon/nitrogen (isotopes). The carbon/nitrogen isotope data provide valuable ...

2012-10-02T23:59:59.000Z

205

Selection of Isotopes and Elements for Fuel Cycle Analysis  

Science Conference Proceedings (OSTI)

Fuel cycle system analysis simulations examine how the selection among fuel cycle options for reactors, fuel, separation, and waste management impact uranium ore utilization, waste masses and volumes, radiotoxicity, heat to geologic repositories, isotope-dependent proliferation resistance measures, and so forth. Previously, such simulations have tended to track only a few actinide and fission product isotopes, those that have been identified as important to a few criteria from the standpoint of recycled material or waste, taken as a whole. After accounting for such isotopes, the residual mass is often characterized as “fission product other” or “actinide other”. However, detailed assessment of separation and waste management options now require identification of key isotopes and residual mass for Group 1A/2A elements (Rb, Cs, Sr, Ba), inert gases (Kr, Xe), halogens (Br, I), lanthanides, transition metals, transuranic (TRU), uranium, actinide decay products. The paper explains the rationale for a list of 81 isotopes and chemical elements to better support separation and waste management assessment in dynamic system analysis models such as Verifiable Fuel Cycle Simulation (VISION)

Steven J. Piet

2009-04-01T23:59:59.000Z

206

Hydrogen Isotope Exchange Properties of Porous Solids Containing Hydrogen  

Science Conference Proceedings (OSTI)

Porous solids such as activated alumina, silica and molecular sieves generally contain significant amounts of hydrogen atoms in the form of H2O or OH even at high temperature and low humidity environment. A significant amount of this hydrogen is available for reversible isotopic exchange. This exchange reaction is slow under normal conditions and does not render itself to practical applications. But if the exchange kinetics is improved this reaction has the potential to be used for tritium removal from gas streams or for hydrogen isotopic separation.The use of catalysts to improve the exchange kinetics between hydrogen isotope in the gas phase and that in the solid phase was investigated. Granules of alumina, silica and molecular sieve were coated with platinum or palladium as the catalyst. The granules were packed in a 2-cm diameter column for isotope exchange tests. Gas streams containing different concentrations of deuterium in nitrogen or argon were fed through the protium saturated column. Isotope concentration in column effluent was monitored to generate isotope break-through curves. The curves were analyzed to produce information on the kinetics and capacity of the material. The results showed that all materials tested provided some extent of isotope exchange but some were superior both in kinetics and capacity. This paper will present the test results.

HEUNG, LEUNGK.

2004-08-18T23:59:59.000Z

207

Laser system using regenerative amplifier  

DOE Patents (OSTI)

High energy laser system using a regenerative amplifier, which relaxes all constraints on laser components other than the intrinsic damage level of matter, so as to enable use of available laser system components. This can be accomplished by use of segmented components, spatial filters, at least one amplifier using solid state or gaseous media, and separated reflector members providing a long round trip time through the regenerative cavity, thereby allowing slower switching and adequate time to clear the spatial filters, etc. The laser system simplifies component requirements and reduces component cost while providing high energy output.

Emmett, John L. (Pleasanton, CA)

1980-01-01T23:59:59.000Z

208

Laser system using regenerative amplifier  

DOE Patents (OSTI)

High energy laser system is disclosed using a regenerative amplifier, which relaxes all constraints on laser components other than the intrinsic damage level of matter, so as to enable use of available laser system components. This can be accomplished by use of segmented components, spatial filters, at least one amplifier using solid state or gaseous media, and separated reflector members providing a long round trip time through the regenerative cavity, thereby allowing slower switching and adequate time to clear the spatial filters, etc. The laser system simplifies component requirements and reduces component cost while providing high energy output. 10 figs.

Emmett, J.L.

1980-03-04T23:59:59.000Z

209

Stable Isotopes in Hailstones. Part I: The Isotopic Cloud Model  

Science Conference Proceedings (OSTI)

Equations describing the isotopic balance between five water species (vapor, cloud water, rainwater, cloud ice and graupel)have been incorporated into a one-dimensional steady-state cloud model. The isotope contents of the various water ...

B. Federer; N. Brichet; J. Jouzel

1982-06-01T23:59:59.000Z

210

Relational separation logic  

Science Conference Proceedings (OSTI)

In this paper, we present a Hoare-style logic for specifying and verifying how two pointer programs are related. Our logic lifts the main features of separation logic, from an assertion to a relation, and from a property about a single program to a relationship ... Keywords: Program verification, Relational reasoning, Schorr—Waite graph marking algorithm, Separation logic

Hongseok Yang

2007-05-01T23:59:59.000Z

211

URANIUM SEPARATION PROCESS  

DOE Patents (OSTI)

The separation of uranium from an aqueous solution containing a water soluble uranyl salt is described. The process involves adding an alkali thiocyanate to the aqueous solution, contacting the resulting solution with methyl isobutyl ketons and separating the resulting aqueous and organic phase. The uranium is extracted in the organic phase as UO/sub 2/(SCN)/sub/.

McVey, W.H.; Reas, W.H.

1959-03-10T23:59:59.000Z

212

Laser Ignition  

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

Laser Ignition Laser Ignition Laser Ignition A first excitation laser or other excitation light source is used in tandem with an ignitor laser to provide a compact, durable, engine deployable fuel ignition laser system. Available for thumbnail of Feynman Center (505) 665-9090 Email Laser Ignition A first excitation laser or other excitation light source is used in tandem with an ignitor laser to provide a compact, durable, engine deployable fuel ignition laser system. Reliable fuel ignition is provided over a wide range of fuel conditions by using a single remote excitation light source for one or more small lasers located proximate to one or more fuel combustion zones. In two embodiments the beam from the excitation light source is split with a portion of it going to the ignitor laser and a second portion

213

Substituted polyacetylene separation membrane  

DOE Patents (OSTI)

A separation membrane useful for gas separation, particularly separation of C.sub.2+ hydrocarbons from natural gas. The invention encompasses the membrane itself, methods of making it and processes for using it. The membrane comprises a polymer having repeating units of a hydrocarbon-based, disubstituted polyacetylene, having the general formula: ##STR1## wherein R.sub.1 is chosen from the group consisting of C.sub.1 -C.sub.4 alkyl and phenyl, and wherein R.sub.2 is chosen from the group consisting of hydrogen and phenyl. In the most preferred embodiment, the membrane comprises poly(4-methyl-2-pentyne) ›PMP!. The membrane exhibits good chemical resistance and has super-glassy properties with regard to separating certain large, condensable permeant species from smaller, less-condensable permeant species. The membranes may also be useful in other fluid separations.

Pinnau, Ingo (Palo Alto, CA); Morisato, Atsushi (Tokyo, JP)

1998-01-13T23:59:59.000Z

214

Separators for flywheel rotors  

DOE Patents (OSTI)

A separator forms a connection between the rotors of a concentric rotor assembly. This separator allows for the relatively free expansion of outer rotors away from inner rotors while providing a connection between the rotors that is strong enough to prevent disassembly. The rotor assembly includes at least two rotors referred to as inner and outer flywheel rings or rotors. This combination of inner flywheel ring, separator, and outer flywheel ring may be nested to include an arbitrary number of concentric rings. The separator may be a segmented or continuous ring that abuts the ends of the inner rotor and the inner bore of the outer rotor. It is supported against centrifugal loads by the outer rotor and is affixed to the outer rotor. The separator is allowed to slide with respect to the inner rotor. It is made of a material that has a modulus of elasticity that is lower than that of the rotors. 10 figs.

Bender, D.A.; Kuklo, T.C.

1998-07-07T23:59:59.000Z

215

Separators for flywheel rotors  

DOE Patents (OSTI)

A separator forms a connection between the rotors of a concentric rotor assembly. This separator allows for the relatively free expansion of outer rotors away from inner rotors while providing a connection between the rotors that is strong enough to prevent disassembly. The rotor assembly includes at least two rotors referred to as inner and outer flywheel rings or rotors. This combination of inner flywheel ring, separator, and outer flywheel ring may be nested to include an arbitrary number of concentric rings. The separator may be a segmented or continuous ring that abuts the ends of the inner rotor and the inner bore of the outer rotor. It is supported against centrifugal loads by the outer rotor and is affixed to the outer rotor. The separator is allowed to slide with respect to the inner rotor. It is made of a material that has a modulus of elasticity that is lower than that of the rotors.

Bender, Donald A. (Dublin, CA); Kuklo, Thomas C. (Oakdale, CA)

1998-01-01T23:59:59.000Z

216

Substituted polyacetylene separation membrane  

DOE Patents (OSTI)

A separation membrane is described which is useful for gas separation, particularly separation of C{sub 2+} hydrocarbons from natural gas. The invention encompasses the membrane itself, methods of making it and processes for using it. The membrane comprises a polymer having repeating units of a hydrocarbon-based, disubstituted polyacetylene, having the general formula shown in the accompanying diagram, wherein R{sub 1} is chosen from the group consisting of C{sub 1}-C{sub 4} alkyl and phenyl, and wherein R{sub 2} is chosen from the group consisting of hydrogen and phenyl. In the most preferred embodiment, the membrane comprises poly(4-methyl-2-pentyne) [PMP]. The membrane exhibits good chemical resistance and has super-glassy properties with regard to separating certain large, condensable permeant species from smaller, less-condensable permeant species. The membranes may also be useful in other fluid separations. 4 figs.

Pinnau, I.; Morisato, Atsushi

1998-01-13T23:59:59.000Z

217

Atom probe microscopy of three-dimensional distribution of silicon isotopes in {sup 28}Si/{sup 30}Si isotope superlattices with sub-nanometer spatial resolution  

Science Conference Proceedings (OSTI)

Laser-assisted atom probe microscopy of 2 nm period {sup 28}Si/{sup 30}Si isotope superlattices (SLs) is reported. Three-dimensional distributions of {sup 28}Si and {sup 30}Si stable isotopes are obtained with sub-nanometer spatial resolution. The depth resolution of the present atom probe analysis is much higher than that of secondary ion mass spectrometry (SIMS) even when SIMS is performed with a great care to reduce the artifact due to atomic mixing. Outlook of Si isotope SLs as ideal depth scales for SIMS and three-dimensional position standards for atom probe microscopy is discussed.

Shimizu, Yasuo; Kawamura, Yoko; Uematsu, Masashi; Itoh, Kohei M. [School of Fundamental Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama 223-8522 (Japan); Tomita, Mitsuhiro [Corporate Research and Development Center, Toshiba Corporation, 8 Shinsugita-cho, Isogo-ku, Yokohama 235-8522 (Japan); Sasaki, Mikio; Uchida, Hiroshi; Takahashi, Mamoru [Toshiba Nanoanalysis Corporation, 1 Komukai Toshiba-cho, Saiwai-ku, Kawasaki 212-8583 (Japan)

2009-10-01T23:59:59.000Z

218

Laser Radiometry  

Science Conference Proceedings (OSTI)

... over a wide range of powers, energies, and wavelengths. ... the SI units for laser power and energy. ... Novel power meter for high-efficiency laser diode ...

2012-04-18T23:59:59.000Z

219

DEEP WATER ISOTOPIC CURRENT ANALYZER  

DOE Patents (OSTI)

A deepwater isotopic current analyzer, which employs radioactive isotopes for measurement of ocean currents at various levels beneath the sea, is described. The apparatus, which can determine the direction and velocity of liquid currents, comprises a shaft having a plurality of radiation detectors extending equidistant radially therefrom, means for releasing radioactive isotopes from the shaft, and means for determining the time required for the isotope to reach a particular detector. (AEC)

Johnston, W.H.

1964-04-21T23:59:59.000Z

220

Separation by solvent extraction  

DOE Patents (OSTI)

17. A process for separating fission product values from uranium and plutonium values contained in an aqueous solution, comprising adding an oxidizing agent to said solution to secure uranium and plutonium in their hexavalent state; contacting said aqueous solution with a substantially water-immiscible organic solvent while agitating and maintaining the temperature at from -1.degree. to -2.degree. C. until the major part of the water present is frozen; continuously separating a solid ice phase as it is formed; separating a remaining aqueous liquid phase containing fission product values and a solvent phase containing plutonium and uranium values from each other; melting at least the last obtained part of said ice phase and adding it to said separated liquid phase; and treating the resulting liquid with a new supply of solvent whereby it is practically depleted of uranium and plutonium.

Holt, Jr., Charles H. (Kennewick, WA)

1976-04-06T23:59:59.000Z

Note: This page contains sample records for the topic "laser isotope separation" 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

Optimal distance separating halfspace  

E-Print Network (OSTI)

Plastria & Carrizosa / Optimal distance separating halfspace. 2. 1 Gauge Distance to a Hyperplane. Let ? be a gauge on Rd with unit ball B, i.e. B is a compact ...

222

Gas-separation process  

DOE Patents (OSTI)

A process for separating condensable organic components from gas streams. The process makes use of a membrane made from a polymer material that is glassy and that has an unusually high free volume within the polymer material.

Toy, Lora G. (San Francisco, CA); Pinnau, Ingo (Palo Alto, CA); Baker, Richard W. (Palo Alto, CA)

1994-01-01T23:59:59.000Z

223

Molten salt electrolyte separator  

DOE Patents (OSTI)

A molten salt electrolyte/separator for battery and related electrochemical systems including a molten electrolyte composition and an electrically insulating solid salt dispersed therein, to provide improved performance at higher current densities and alternate designs through ease of fabrication.

Kaun, Thomas D. (New Lenox, IL)

1996-01-01T23:59:59.000Z

224

successfully demonstrated the separation  

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

successfully demonstrated the separation and capture of 90 percent successfully demonstrated the separation and capture of 90 percent of the c arbon dioxide (CO 2 ) from a pulve rized coal plant. In t he ARRA-funded project, Membrane Technology and Research Inc. (MTR) and its partners tested the Polaris(tm) membrane system, which uses a CO 2 -selective polymeric membrane material and module to capture CO 2 from a plant's flue gas. Since the Polaris(tm) membranes

225

Nuclear charge radii of potassium isotopes beyond N=28  

E-Print Network (OSTI)

We report on the measurement of optical isotope shifts for $^{38,39,42,44,46\\text{-}51}$K relative to $^{47}$K from which changes in the nuclear mean square charge radii across the N=28 shell closure are deduced. The investigation was carried out by bunched-beam collinear laser spectroscopy at the CERN-ISOLDE radioactive ion-beam facility. Mean square charge radii are now known from $^{37}$K to $^{51}$K, covering all $\

Kreim, K; Papuga, J; Blaum, K; De Rydt, M; Ruiz, R F Garcia; Goriely, S; Heylen, H; Kowalska, M; Neugart, R; Neyens, G; Nörtershäuser, W; Rajabali, M M; Alarcón, R Sánchez; Stroke, H H; Yordanov, D T

2013-01-01T23:59:59.000Z

226

SEPARATION OF FLUID MIXTURES  

DOE Patents (OSTI)

An apparatus is presented for separating gaseous mixtures by selectively freezing a constituent of the mixture and subsequently separating the frozen gas. The gas mixture is passed through a cylinder fltted with a cooling jacket, causing one gas to freeze on the walls of the cylinder. A set of scraper blades are provided in the interior of the cyllnder, and as the blades oscillate, the frozen gas is scraped to the bottom of the cylinder. Means are provided for the frozen material to pass into a heating chamber where it is vaporized and the product gas collected.

Lipscomb, R.; Craig, A.; Labrow, S.; Dunn, J.F.

1958-10-28T23:59:59.000Z

227

WET FLUORIDE SEPARATION METHOD  

DOE Patents (OSTI)

The separation of U/sup 233/ from thorium, protactinium, and fission products present in neutron-irradiated thorium is accomplished by dissolving the irradiated materials in aqueous nitric acid, adding either a soluble fluoride, iodate, phosphate, or oxalate to precipltate the thorium, separating the precipltate from the solution, and then precipitating uranlum and protactinium by alkalizing the solution. The uranium and protactinium precipitate is removcd from the solution and dissolved in nitric acid. The uranyl nitrate may then be extracted from the acid solution by means of ether, and the protactinium recovered from the aqueous phase.

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

1958-11-25T23:59:59.000Z

228

Interpretation of Water Chemistry and Stable Isotope Data from a Karst Aquifer According to Flow Regimes Identified through Hydrograph  

E-Print Network (OSTI)

82 Interpretation of Water Chemistry and Stable Isotope Data from a Karst Aquifer According to Flow.S. Geological Survey, 345 Middlefield Rd., MS 434, Menlo Park, CA, 94025 2 Univ. of Minnesota, Dept. of Geology for the identification of four separate flow regimes of the aquifer outflow. Major ion chemistry and stable isotopic

229

Gas-separation process  

DOE Patents (OSTI)

A process is described for separating condensable organic components from gas streams. The process makes use of a membrane made from a polymer material that is glassy and that has an unusually high free volume within the polymer material. 6 figures.

Toy, L.G.; Pinnau, I.; Baker, R.W.

1994-01-25T23:59:59.000Z

230

SEPARATION BY ADSORPTION  

DOE Patents (OSTI)

Separation of Pu from fission products by adsorption on hydrous aluminum silicate is described. The Pu in a HNO/sub 3/ solution is oxidized to the hexavalent state and contacted with the silicate which adsorbs fission products. (T.R.H.)

Lowe, C.S.

1959-06-16T23:59:59.000Z

231

NEAMS safeguards and separations  

Science Conference Proceedings (OSTI)

This presentation provides a program management update on the Safeguards and Separations Integrated Performance and Safety Code (IPSC) program in the DOE Nuclear Energy Advanced Modeling and Simulation (NEAMS). It provides an overview of FY11 work packages at multiple DOE Labs and includes material on challenge problem definitions for the IPSC effort.

Sadasivan, Pratap [Los Alamos National Laboratory; De Paoli, David W [ORNL

2011-01-25T23:59:59.000Z

232

Molten salt electrolyte separator  

DOE Patents (OSTI)

The patent describes a molten salt electrolyte/separator for battery and related electrochemical systems including a molten electrolyte composition and an electrically insulating solid salt dispersed therein, to provide improved performance at higher current densities and alternate designs through ease of fabrication. 5 figs.

Kaun, T.D.

1996-07-09T23:59:59.000Z

233

Mesoporous Block Copolymer Battery Separators  

E-Print Network (OSTI)

is ~1-2 $ kg -1 , the cost of battery separators is ~120-240greatly reduce the cost of battery separators. Our approach1-2 $ kg -1 , the cost of a typical battery separator is in

Wong, David Tunmin

2012-01-01T23:59:59.000Z

234

Isotopically labeled compositions and method  

DOE Patents (OSTI)

Compounds having stable isotopes .sup.13C and/or .sup.2H were synthesized from precursor compositions having solid phase supports or affinity tags.

Schmidt, Jurgen G. (Los Alamos, NM); Kimball, David B. (Los Alamos, NM); Alvarez, Marc A. (Santa Fe, NM); Williams, Robert F. (Los Alamos, NM); Martinez, Rudolfo A. (Santa Fe, NM)

2011-07-12T23:59:59.000Z

235

Unattended Environmental Sampling and Laser-based Enrichment Assay for Detection of Undeclared HEU Production in Enrichment Plants  

Science Conference Proceedings (OSTI)

Nuclear power is enjoying rapid growth as government energy policies and public demand shift toward carbon neutral energy production. Accompanying the growth in nuclear power is the requirement for increased nuclear fuel production, including a significant expansion in uranium enrichment capacity. Essential to the success of the nuclear energy renaissance is the development and implementation of sustainable, proliferation-resistant nuclear power generation. Unauthorized production of highly enriched uranium (HEU) remains the primary proliferation concern for modern gaseous centrifuge enrichment plants (GCEPs). While to date there has been no indication of declared, safeguarded GCEPs producing HEU, the massive separative work unit (SWU) processing power of modern GCEPs presents a significant latent risk of nuclear breakout and suggests the need for more timely detection of potential facility misuse. The Pacific Northwest National Laboratory is developing an unattended safeguards instrument, combining continuous aerosol particulate collection with uranium isotope assay, to provide timely HEU detection within a GCEP. This approach is based on laser vaporization of aerosol particulates, followed by laser spectroscopy to characterize the uranium enrichment level. We demonstrate enrichment assay, with relative isotope abundance uncertainty <5%, on individual micron-sized particles that are trace components within a mixture ‘background’ particles

Anheier, Norman C.; Bushaw, Bruce A.

2010-04-15T23:59:59.000Z

236

Isotope Production and Distribution Program. Financial statements, September 30, 1994 and 1993  

SciTech Connect

The attached report presents the results of the independent certified public accountants` audit of the Isotope Production and Distribution (IP&D) Program`s financial statements as of September 30, 1994. The auditors have expressed an unqualified opinion on IP&D`s 1994 statements. Their reports on IP&D`s internal control structure and on compliance with laws,and regulations are also provided. The charter of the Isotope Program covers the production and sale of radioactive and stable isotopes, byproducts, and related isotope services. Prior to October 1, 1989, the Program was subsidized by the Department of Energy through a combination of appropriated funds and isotope sales revenue. The Fiscal Year 1990 Appropriations Act, Public Law 101-101, authorized a separate Isotope Revolving Fund account for the Program, which was to support itself solely from the proceeds of isotope sales. The initial capitalization was about $16 million plus the value of the isotope assets in inventory or on loan for research and the unexpended appropriation available at the close of FY 1989. During late FY 1994, Public Law 103--316 restructured the Program to provide for supplemental appropriations to cover costs which are impractical to incorporate into the selling price of isotopes. Additional information about the Program is provided in the notes to the financial statements.

Marwick, P.

1994-11-30T23:59:59.000Z

237

Laser Spectro.  

Science Conference Proceedings (OSTI)

For more information about my work on laser spectroscopy, consult the following papers: Sansonetti, CJ, Gillaspy, JD, and ...

238

Steam separator latch assembly  

SciTech Connect

A latch assembly removably joins a steam separator assembly to a support flange disposed at a top end of a tubular shroud in a nuclear reactor pressure vessel. The assembly includes an annular head having a central portion for supporting the steam separator assembly thereon, and an annular head flange extending around a perimeter thereof for supporting the head to the support flange. A plurality of latches are circumferentially spaced apart around the head flange with each latch having a top end, a latch hook at a bottom end thereof, and a pivot support disposed at an intermediate portion therebetween and pivotally joined to the head flange. The latches are pivoted about the pivot supports for selectively engaging and disengaging the latch hooks with the support flange for fixedly joining the head to the shroud or for allowing removal thereof.

Challberg, Roy C. (Livermore, CA); Kobsa, Irvin R. (San Jose, CA)

1994-01-01T23:59:59.000Z

239

Steam separator latch assembly  

DOE Patents (OSTI)

A latch assembly removably joins a steam separator assembly to a support flange disposed at a top end of a tubular shroud in a nuclear reactor pressure vessel. The assembly includes an annular head having a central portion for supporting the steam separator assembly thereon, and an annular head flange extending around a perimeter thereof for supporting the head to the support flange. A plurality of latches are circumferentially spaced apart around the head flange with each latch having a top end, a latch hook at a bottom end thereof, and a pivot support disposed at an intermediate portion therebetween and pivotally joined to the head flange. The latches are pivoted about the pivot supports for selectively engaging and disengaging the latch hooks with the support flange for fixedly joining the head to the shroud or for allowing removal thereof. 12 figures.

Challberg, R.C.; Kobsa, I.R.

1994-02-01T23:59:59.000Z

240

Advanced Separation Consortium  

Science Conference Proceedings (OSTI)

The Center for Advanced Separation Technologies (CAST) was formed in 2001 under the sponsorship of the US Department of Energy to conduct fundamental research in advanced separation and to develop technologies that can be used to produce coal and minerals in an efficient and environmentally acceptable manner. The CAST consortium consists of seven universities - Virginia Tech, West Virginia University, University of Kentucky, Montana Tech, University of Utah, University of Nevada-Reno, and New Mexico Tech. The consortium brings together a broad range of expertise to solve problems facing the US coal industry and the mining sector in general. At present, a total of 60 research projects are under way. The article outlines some of these, on topics including innovative dewatering technologies, removal of mercury and other impurities, and modelling of the flotation process. 1 photo.

NONE

2006-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "laser isotope separation" 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

URANIUM SEPARATION PROCESS  

DOE Patents (OSTI)

A method of separating uranium oxides from PuO/sub 2/, ThO/sub 2/, and other actinide oxides is described. The oxide mixture is suspended in a fused salt melt and a chlorinating agent such as chlorine gas or phosgene is sparged through the suspension. Uranium oxides are selectively chlorinated and dissolve in the melt, which may then be filtered to remove the unchlorinated oxides of the other actinides. (AEC)

Lyon, W.L.

1962-04-17T23:59:59.000Z

242

SLA battery separators  

SciTech Connect

Since they first appeared in the early 1970's, sealed lead acid (SLA) batteries have been a rapidly growing factor in the battery industry - in rechargeable, deep-cycle, and automotive storage systems. The key to these sealed batteries is the binderless, absorptive glass microfiber separator which permits the electrolyte to recombine after oxidation. The result is no free acid, no outgassing, and longer life. The batteries are described.

Fujita, Y.

1986-10-01T23:59:59.000Z

243

Cell separator and cell  

SciTech Connect

There is disclosed a novel cell separator made of a grafted membrane comprising a polyethylene film which is graft copolymerized with a monomer having an ion exchange group, characterized in that said membrane has an area which is not grafted at all or an area of low degree grafting. By making use of this membrane, a small size and thin cell having excellent performance as well as satisfactory mechanical strength can be produced at low cost with great advantages.

Ishigaki, I.; Machi, S.; Murata, K.; Okada, T.; Senoo, K.; Sugo, T.; Tanso, S.

1981-09-01T23:59:59.000Z

244

United States Department of Energy Office of Nuclear Energy, Isotope Production and Distribution Program financial statements, September 30, 1996 and 1995  

Science Conference Proceedings (OSTI)

The charter of the Department of Energy (DOE) Isotope Production and Distribution Program (Isotope Program) covers the production and sale of radioactive and stable isotopes, associated byproducts, surplus materials such as lithium, and related isotope services. Service provided include, but are not limited to, irradiation services, target preparation and processing, source encapsulation and other special preparations, analyses, chemical separations, and leasing of stable isotopes for research purposes. Isotope Program products and services are sold worldwide for use in a wide variety of research, development, biomedical, and industrial applications. This report presents the results of the independent certified public accountants` audit of the Isotope Production and Distribution Program`s (Isotope) financial statements as of September 30, 1996.

NONE

1997-04-01T23:59:59.000Z

245

Innovative Separations Technologies  

Science Conference Proceedings (OSTI)

Reprocessing used nuclear fuel (UNF) is a multi-faceted problem involving chemistry, material properties, and engineering. Technology options are available to meet a variety of processing goals. A decision about which reprocessing method is best depends significantly on the process attributes considered to be a priority. New methods of reprocessing that could provide advantages over the aqueous Plutonium Uranium Reduction Extraction (PUREX) and Uranium Extraction + (UREX+) processes, electrochemical, and other approaches are under investigation in the Fuel Cycle Research and Development (FCR&D) Separations Campaign. In an attempt to develop a revolutionary approach to UNF recycle that may have more favorable characteristics than existing technologies, five innovative separations projects have been initiated. These include: (1) Nitrogen Trifluoride for UNF Processing; (2) Reactive Fluoride Gas (SF6) for UNF Processing; (3) Dry Head-end Nitration Processing; (4) Chlorination Processing of UNF; and (5) Enhanced Oxidation/Chlorination Processing of UNF. This report provides a description of the proposed processes, explores how they fit into the Modified Open Cycle (MOC) and Full Recycle (FR) fuel cycles, and identifies performance differences when compared to 'reference' advanced aqueous and fluoride volatility separations cases. To be able to highlight the key changes to the reference case, general background on advanced aqueous solvent extraction, advanced oxidative processes (e.g., volumetric oxidation, or 'voloxidation,' which is high temperature reaction of oxide UNF with oxygen, or modified using other oxidizing and reducing gases), and fluorination and chlorination processes is provided.

J. Tripp; N. Soelberg; R. Wigeland

2011-05-01T23:59:59.000Z

246

ISOTOPE FRACTIONATION PROCESS  

DOE Patents (OSTI)

A new method is described for isotopic enrichment of uranium. It has been found that when an aqueous acidic solution of ionic tetravalent uraniunn is contacted with chelate complexed tetravalent uranium, the U/sup 238/ preferentially concentrates in the complexed phase while U/sup 235/ concentrates in the ionic phase. The effect is enhanced when the chelate compound is water insoluble and is dissolved in a water-immiscible organic solvent. Cupferron is one of a number of sultable complexing agents, and chloroform is a suitable organic solvent.

Clewett, G.H.; Lee, DeW.A.

1958-05-20T23:59:59.000Z

247

Evolution of isotopic composition of reprocessed uranium during the multiple recycling in light water reactors with natural uranium feed  

Science Conference Proceedings (OSTI)

A complex approach based on the consistent modeling of neutron-physics processes and processes of cascade separation of isotopes is applied for analyzing physical problems of the multiple usage of reprocessed uranium in the fuel cycle of light water reactors. A number of scenarios of multiple recycling of reprocessed uranium in light water reactors are considered. In the process, an excess absorption of neutrons by the {sup 236}U isotope is compensated by re-enrichment in the {sup 235}U isotope. Specific consumptions of natural uranium for re-enrichment of the reprocessed uranium depending on the content of the {sup 232}U isotope are obtained.

Smirnov, A. Yu., E-mail: a.y.smirnoff@rambler.ru; Sulaberidze, G. A. [National Research Nuclear University MEPhI (Russian Federation); Alekseev, P. N.; Dudnikov, A. A.; Nevinitsa, V. A., E-mail: neva@dhtp.kiae.ru; Proselkov, V. N.; Chibinyaev, A. V. [Russian Research Centre Kurchatov Institute (Russian Federation)

2012-12-15T23:59:59.000Z

248

Development of high through-put Sr isotope analysis for monitoring reservoir integrity for CO{sub 2} storage.  

SciTech Connect

Recent innovations in multi-collector ICP-mass spectrometry (MC-ICP-MS) have allowed for rapid and precise measurements of isotope ratios in geological samples. Naturally occurring Sr isotopes has the potential for use in Monitoring, Verification, and Accounting (MVA) associated with geologic CO2 storage. Sr isotopes can be useful for: Sensitive tracking of brine migration; Determining seal rock leakage; Studying fluid/rock reactions. We have optimized separation chemistry procedures that will allow operators to prepare samples for Sr isotope analysis off site using rapid, low cost methods.

Wall, Andy; Jain, Jinesh; Stewart, Brian; Capo, Rosemary; Hakala, Alexandra J.; Hammack, Richard; Guthrie, George

2012-01-01T23:59:59.000Z

249

The athermal Laser  

E-Print Network (OSTI)

A new laser concept is presented, called the athermal laser, unifying all the hitherto known implementations of radiative laser cooling.

Muys, Peter

2009-01-01T23:59:59.000Z

250

Isotopic Analysis- Fluid | Open Energy Information  

Open Energy Info (EERE)

Isotopic Analysis- Fluid Isotopic Analysis- Fluid Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Technique: Isotopic Analysis- Fluid Details Activities (61) Areas (32) Regions (6) NEPA(0) Exploration Technique Information Exploration Group: Lab Analysis Techniques Exploration Sub Group: Fluid Lab Analysis Parent Exploration Technique: Fluid Lab Analysis Information Provided by Technique Lithology: Water rock interaction Stratigraphic/Structural: Hydrological: Origin of hydrothermal fluids; Mixing of hydrothermal fluids Thermal: Isotopic ratios can be used to characterize and locate subsurface thermal anomalies. Dictionary.png Isotopic Analysis- Fluid: Isotopes are atoms of the same element that have different numbers of neutrons. An isotopic analysis looks at a particular isotopic element(s) in

251

It's Elemental - Isotopes of the Element Neptunium  

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

Uranium Previous Element (Uranium) The Periodic Table of Elements Next Element (Plutonium) Plutonium Isotopes of the Element Neptunium Click for Main Data Most of the isotope...

252

It's Elemental - Isotopes of the Element Sulfur  

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

Phosphorus Previous Element (Phosphorus) The Periodic Table of Elements Next Element (Chlorine) Chlorine Isotopes of the Element Sulfur Click for Main Data Most of the isotope...

253

It's Elemental - Isotopes of the Element Argon  

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

Chlorine Previous Element (Chlorine) The Periodic Table of Elements Next Element (Potassium) Potassium Isotopes of the Element Argon Click for Main Data Most of the isotope data...

254

The marine biogeochemistry of zinc isotopes  

E-Print Network (OSTI)

Zinc (Zn) stable isotopes can record information about important oceanographic processes. This thesis presents data on Zn isotopes in anthropogenic materials, hydrothermal fluids and minerals, cultured marine phytoplankton, ...

John, Seth G

2007-01-01T23:59:59.000Z

255

It's Elemental - Isotopes of the Element Ruthenium  

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

Technetium Previous Element (Technetium) The Periodic Table of Elements Next Element (Rhodium) Rhodium Isotopes of the Element Ruthenium Click for Main Data Most of the isotope...

256

It's Elemental - Isotopes of the Element Molybdenum  

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

Niobium Previous Element (Niobium) The Periodic Table of Elements Next Element (Technetium) Technetium Isotopes of the Element Molybdenum Click for Main Data Most of the isotope...

257

It's Elemental - Isotopes of the Element Thorium  

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

Table of Elements Next Element (Protactinium) Protactinium Isotopes of the Element Thorium Click for Main Data Most of the isotope data on this site has been obtained from...

258

It's Elemental - Isotopes of the Element Protactinium  

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

Thorium Previous Element (Thorium) The Periodic Table of Elements Next Element (Uranium) Uranium Isotopes of the Element Protactinium Click for Main Data Most of the isotope data...

259

High-Precision Isotopic Reference Materials  

Science Conference Proceedings (OSTI)

... sources, is now capable of measuring isotope ratios with ... revolution in the use of isotopes by revealing ... This program will have an impact in several ...

2012-10-22T23:59:59.000Z

260

NETL: Gasification Systems - Gas Separation  

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

Separation Separation Ion-Transport Membrane Oxygen Separation Modules Ion-Transport Membrane Oxygen Separation Modules Gas separation unit operations represent major cost elements in gasification plants. The gas separation technology being supported in the DOE program promises significant reduction in cost of electricity, improved thermal efficiency, and superior environmental performance. Gasification-based energy conversion systems rely on two gas separation processes: (1) separation of oxygen from air for feed to oxygen-blown gasifiers; and (2) post-gasification separation of hydrogen from carbon dioxide following (or along with) the shifting of gas composition when carbon dioxide capture is required or hydrogen is the desired product. Research efforts include development of advanced gas separation

Note: This page contains sample records for the topic "laser isotope separation" 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

Means and method of detection in chemical separation procedures  

DOE Patents (OSTI)

A means and method for indirect detection of constituent components of a mixture separated in a chemical separation process. Fluorescing ions are distributed across the area in which separation of the mixture will occur to provide a generally uniform background fluorescence intensity. For example, the mixture is comprised of one or more charged analytes which displace fluorescing ions where its constituent components separate to. Fluorescing ions of the same charge as the charged analyte components cause a displacement. The displacement results in the location of the separated components having a reduced fluorescence intensity to the remainder of the background. Detection of the lower fluorescence intensity areas can be visually, by photographic means and methods, or by automated laser scanning.

Yeung, Edward S. (Ames, IA); Koutny, Lance B. (Ames, IA); Hogan, Barry L. (Ames, IA); Cheung, Chan K. (Ames, IA); Ma, Yinfa (Ames, IA)

1993-03-09T23:59:59.000Z

262

TRImP - A new facility to produce and trap radioactive isotopes  

E-Print Network (OSTI)

At the Kernfysisch Vensneller Institiutr (KVI) in Groningen, NL, a new facility (TRImP) is under development. It aims for producing, slowing down, and trapping of radioactive isotopes in order to perform accurate measurements on fundamental symmetries and interactions. A production target station and a dual magnetic separator installed and commissioned. We will slow down the isotopes of interest using an ion catcher and in a further stage a radiofrequency quadropole gas cooler (RFQ). The isotopes will finally be trapped in an atomic trap for precision studies.

Sohani, M

2006-01-01T23:59:59.000Z

263

TRImP - A new facility to produce and trap radioactive isotopes  

E-Print Network (OSTI)

At the Kernfysisch Vensneller Institiutr (KVI) in Groningen, NL, a new facility (TRImP) is under development. It aims for producing, slowing down, and trapping of radioactive isotopes in order to perform accurate measurements on fundamental symmetries and interactions. A production target station and a dual magnetic separator installed and commissioned. We will slow down the isotopes of interest using an ion catcher and in a further stage a radiofrequency quadropole gas cooler (RFQ). The isotopes will finally be trapped in an atomic trap for precision studies.

M. Sohani

2006-01-17T23:59:59.000Z

264

Isotope and Nuclear Chemistry Division annual report FY 1986, October 1985-September 1986  

Science Conference Proceedings (OSTI)

This report describes progress in the major research and development programs carried out in FY 1986 by the Isotope and Nuclear Chemistry Division. The report includes articles on radiochemical diagnostics and weapons tests; weapons radiochemical diagnostics research and development; other unclassified weapons research; stable and radioactive isotope production and separation; chemical biology and nuclear medicine; element and isotope transport and fixation; actinide and transition metal chemistry; structural chemistry, spectroscopy, and applications; nuclear structure and reactions; irradiation facilities; advanced concepts and technology; and atmospheric chemistry.

Heiken, J.H. (ed.)

1987-06-01T23:59:59.000Z

265

SEPARATION OF PLUTONIUM  

DOE Patents (OSTI)

A method is described for separating plutonium from uranium and fission products by treating a nitrate solution of fission products, uranium, and hexavalent plutonium with a relatively water-insoluble fluoride to adsorb fission products on the fluoride, treating the residual solution with a reducing agent for plutonium to reduce its valence to four and less, treating the reduced plutonium solution with a relatively insoluble fluoride to adsorb the plutonium on the fluoride, removing the solution, and subsequently treating the fluoride with its adsorbed plutonium with a concentrated aqueous solution of at least one of a group consisting of aluminum nitrate, ferric nitrate, and manganous nitrate to remove the plutonium from the fluoride.

Maddock, A.G.; Smith, F.

1959-08-25T23:59:59.000Z

266

Polymeric battery separators  

SciTech Connect

Configurations of cross-linked or vulcanized amphophilic or quaternized block copolymer of haloalkyl epoxides and hydroxyl terminated alkadiene polymers are useful as battery separators in both primary and secondary batteries, particularly nickel-zinc batteries. The quaternized block copolymers are prepared by polymerizing a haloalkyl epoxide in the presence of a hydroxyl terminated 1,3-alkadiene to form a block copolymer that is then reacted with an amine to form the quaternized or amphophilic block copolymer that is then cured or cross-linked with sulfur, polyamines, metal oxides, organic peroxides and the like.

Minchak, R. J.; Schenk, W. N.

1985-06-11T23:59:59.000Z

267

NIOBIUM-TANTALUM SEPARATION  

DOE Patents (OSTI)

The usual method for the separation of tantalum and niobium consists of a selective solvent extraction from an aqueous hydrofluoric acid solution of the metals. A difficulty encountered in this process is the fact that the corrosion problems associated with hydrofluoric acid are serious. It has been found that the corrosion caused by the hydrofluoric acid may be substantially reduced by adding to the acidic solution an amine, such as phenyl diethanolamine or aniline, and adjusting pH value to between 4 and 6.

Wilhelm, H.A.; Foos, R.A.

1959-01-27T23:59:59.000Z

268

URANIUM SEPARATION PROCESS  

DOE Patents (OSTI)

The separation of uranium from a mixture of uranium and thorium by organic solvent extraction from an aqueous solution is described. The uranium is separrted from an aqueous mixture of uranium and thorium nitrates 3 N in nitric acid and containing salting out agents such as ammonium nitrate, so as to bring ihe total nitrate ion concentration to a maximum of about 8 N by contacting the mixture with an immiscible aliphatic oxygen containing organic solvent such as diethyl carbinol, hexone, n-amyl acetate and the like. The uranium values may be recovered from the organic phase by back extraction with water.

Hyde, E.K.; Katzin, L.I.; Wolf, M.J.

1959-07-14T23:59:59.000Z

269

Vacuum barrier for excimer lasers  

DOE Patents (OSTI)

A barrier for separating the vacuum area of a diode from the pressurized gas area of an excimer laser. The barrier is a composite material comprising layers of a metal such as copper, along with layers of polyimide, and a matrix of graphite fiber yarns impregnated with epoxy. The barrier is stronger than conventional foil barriers, and allows greater electron throughput. 3 figs.

Shurter, R.P.

1992-09-15T23:59:59.000Z

270

Explosively separable casing  

DOE Patents (OSTI)

An explosively separable casing including a cylindrical afterbody and a circular cover for one end of the afterbody is disclosed. The afterbody has a cylindrical tongue extending longitudinally from one end which is matingly received in a corresponding groove in the cover. The groove is sized to provide a pocket between the end of the tongue and the remainder of the groove so that an explosive can be located therein. A seal is also provided between the tongue and the groove for sealing the pocket from the atmosphere. A frangible holding device is utilized to hold the cover to the afterbody. When the explosive is ignited, the increase in pressure in the pocket causes the cover to be accelerated away from the afterbody. Preferably, the inner wall of the afterbody is in the same plane as the inner wall of the tongue to provide a maximum space for storage in the afterbody and the side wall of the cover is thicker than the side wall of the afterbody so as to provide a sufficiently strong surrounding portion for the pocket in which the explosion takes place. The detonator for the explosive is also located on the cover and is carried away with the cover during separation. The seal is preferably located at the longitudinal end of the tongue and has a chevron cross section.

Jacobson, Albin K. (Albuquerque, NM); Rychnovsky, Raymond E. (Livermore, CA); Visbeck, Cornelius N. (Livermore, CA)

1985-01-01T23:59:59.000Z

271

Tritium separation from light and heavy water by bipolar electrolysis  

DOE Green Energy (OSTI)

Use of bipolar electrolysis with countercurrent electrolyte flow to separate hydrogen isotopes was investigated for the removal of tritium from light water effluents or from heavy water moderator. Deuterium-tritium and protium-tritium separation factors occurring on a Pd-25% Ag bipolar electrode were measured to be 2.05 to 2.16 and 11.6 to 12.4 respectively, at current densities between 0.21 and 0.50 A cm/sup -2/, and at 35 to 90/sup 0/C. Current densities up to 0.3 A cm/sup -2/ have been achieved in continuous operation, at 80 to 90/sup 0/C, without significant gas formation on the bipolar electrodes. From the measured overvoltage at the bipolar electrodes and the electrolyte conductivity the power consumption per stage was calculated to be 3.0 kwh/kg H/sub 2/O at 0.2 A cm/sup -2/ and 5.0 kwh/kg H/sub 2/O at 0.5 A cm/sup -2/ current density, compared to 6.4 and 8.0 kwh/kg H/sub 2/O for normal electrolysis. A mathematical model derived for hydrogen isotope separation by bipolar electrolysis, i.e., for a square cascade, accurately describes the results for protium-tritium separation in two laboratory scale, multistage experiments with countercurrent electrolyte flow; the measured tiritum concentration gradient through the cascade agreed with the calculated values.

Ramey, D.W.; Petek, M.; Taylor, R.D.; Kobisk, E.H.; Ramey, J.; Sampson, C.A.

1979-10-01T23:59:59.000Z

272

Laser Probing of Neutron-Rich Nuclei in Light Atoms  

E-Print Network (OSTI)

The neutron-rich 6He and 8He isotopes exhibit an exotic nuclear structure that consists of a tightly bound 4He-like core with additional neutrons orbiting at a relatively large distance, forming a halo. Recent experimental efforts have succeeded in laser trapping and cooling these short-lived, rare helium atoms, and have measured the atomic isotope shifts along the 4He-6He-8He chain by performing laser spectroscopy on individual trapped atoms. Meanwhile, the few-electron atomic structure theory, including relativistic and QED corrections, has reached a comparable degree of accuracy in the calculation of the isotope shifts. In parallel efforts, also by measuring atomic isotope shifts, the nuclear charge radii of lithium and beryllium isotopes have been studied. The techniques employed were resonance ionization spectroscopy on neutral, thermal lithium atoms and collinear laser spectroscopy on beryllium ions. Combining advances in both atomic theory and laser spectroscopy, the charge radii of these light halo nuclei have now been determined for the first time independent of nuclear structure models. The results are compared with the values predicted by a number of nuclear structure calculations, and are used to guide our understanding of the nuclear forces in the extremely neutron-rich environment.

Z. -T. Lu; P. Mueller; G. W. F. Drake; W. Noertershaeuser; Steven C. Pieper; Z. -C. Yan

2013-07-10T23:59:59.000Z

273

Hydrogen isotope exchange in metal hydride columns  

DOE Green Energy (OSTI)

Several metal hydrides were shown to act as chromatographic media for hydrogen isotopes. The procedure was to equilibrate a column of hydride with flowing hydrogen, inject a small quantity of tritium tracer, and observe its elution behavior. Characteristic retention times were found. From these and the extent of widening of the tritium band, the heights equivalent to a theoretical plate could be calculated. Values of around 1 cm were obtained. The following are the metals whose hydrides were studied, together with the temperature ranges in which chromatographic behavior was observed: vanadium, 0 to 70/sup 0/C; zirconium, 500 to 600/sup 0/C; LaNi/sub 5/, -78 to +30/sup 0/C; Mg/sub 2/Ni, 300 to 375/sup 0/C; palladium, 0 to 70/sup 0/C. A dual-temperature isotope separation process based on hydride chromatography was demonstrated. In this, a column was caused to cycle between two temperatures while being supplied with a constant stream of tritium-traced hydrogen. Each half-cycle was continued until ''breakthrough,'' i.e., until the tritium concentration in the effluent was the same as that in the feed. Up to that point, the effluent was enriched or depleted in tritium, by up to 20%.

Wiswall, R; Reilly, J; Bloch, F; Wirsing, E

1977-11-21T23:59:59.000Z

274

METHOD OF SEPARATING PLUTONIUM  

DOE Patents (OSTI)

Plutonium hexafluoride is a satisfactory fluorinating agent and may be reacted with various materials capable of forming fluorides, such as copper, iron, zinc, etc., with consequent formation of the metal fluoride and reduction of the plutonium to the form of a lower fluoride. In accordance with the present invention, it has been found that the reactivity of plutonium hexafluoride with other fluoridizable materials is so great that the process may be used as a method of separating plutonium from mixures containing plutonium hexafluoride and other vaporized fluorides even though the plutonium is present in but minute quantities. This process may be carried out by treating a mixture of fluoride vapors comprising plutonium hexafluoride and fluoride of uranium to selectively reduce the plutonium hexafluoride and convert it to a less volatile fluoride, and then recovering said less volatile fluoride from the vapor by condensation.

Brown, H.S.; Hill, O.F.

1958-02-01T23:59:59.000Z

275

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

276

Stable carbon isotope ratio of polycyclic aromatic hydrocarbons (PAHs) in the environment: validation of isolation and stable carbon isotope analysis methods  

E-Print Network (OSTI)

Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous, toxic contaminants that are released to the environment from various petrogenic and pyrogenic sources. In an effort to more clearly identify and trace sources of PAHs in the environment, purification and compound specific isotope analysis methods were developed to accurately measure the stable carbon isotope ratio of individual PAHs. Development of the method included improving accuracy and precision of the isotopic measurement by producing highly pure extracts using various chromatographic techniques. The method was refined by improving compound separations using purification techniques and high resolution chromatographic columns. The purification method consists of alumina/silica gel column chromatography, gel permeation chromatography and thin layer chromatography. The mean recovery of PAHs after the purification procedure was approximately 80 %. Sample purities after purification were verified by GC/FID and full scan mass spectrometry. To better resolve peaks and provide more accurate stable carbon isotope measurements, various gas chromatographic conditions were evaluated. The precision of the method ranged between 0.08 and 0.43 . The analytical protocols were evaluated to confirm compositional and stable isotopic integrity during purification and stable isotopic analysis. To confirm the utility of the purification and isotope analysis methods, various environmental samples from marine, land and lacustrine environments were analyzed. The isolates were analyzed for the composition and the stable carbon isotope ratios of PAHs. The stable carbon isotope ratio was measured by GC/IRMS and the results, along with quantitative compound compositions, were used to characterize and identify the contaminant sources. The sources of the PAHs in the study areas were differentiated by PAH molecular ratios and confirmed by stable carbon isotope ratios. This study confirms that compound specific isotope analysis of pollutants by GC/IRMS can be used to identify PAH sources in environmental samples. The study also confirms that the purification and stable carbon isotope analysis methods that were developed can be used to accurately measure the stable carbon isotope ratios of PAHs in environmental samples for the purpose of source identification. GC/IRMS measurement of stable isotopic compositions can be an effective fingerprinting method when used in conjunction with traditional molecular composition methods.

Kim, Moon Koo

2004-08-01T23:59:59.000Z

277

Compact hydrogen/helium isotope mass spectrometer  

DOE Patents (OSTI)

The compact hydrogen and helium isotope mass spectrometer of the present invention combines low mass-resolution ion mass spectrometry and beam-foil interaction technology to unambiguously detect and quantify deuterium (D), tritium (T), hydrogen molecule (H.sub.2, HD, D.sub.2, HT, DT, and T.sub.2), .sup.3 He, and .sup.4 He concentrations and concentration variations. The spectrometer provides real-time, high sensitivity, and high accuracy measurements. Currently, no fieldable D or molecular speciation detectors exist. Furthermore, the present spectrometer has a significant advantage over traditional T detectors: no confusion of the measurements by other beta-emitters, and complete separation of atomic and molecular species of equivalent atomic mass (e.g., HD and .sup.3 He).

Funsten, Herbert O. (Los Alamos, NM); McComas, David J. (Los Alamos, NM); Scime, Earl E. (Morgantown, WV)

1996-01-01T23:59:59.000Z

278

Compelling Research Opportunities using Isotopes  

SciTech Connect

Isotopes are vital to the science and technology base of the US economy. Isotopes, both stable and radioactive, are essential tools in the growing science, technology, engineering, and health enterprises of the 21st century. The scientific discoveries and associated advances made as a result of the availability of isotopes today span widely from medicine to biology, physics, chemistry, and a broad range of applications in environmental and material sciences. Isotope issues have become crucial aspects of homeland security. Isotopes are utilized in new resource development, in energy from bio-fuels, petrochemical and nuclear fuels, in drug discovery, health care therapies and diagnostics, in nutrition, in agriculture, and in many other areas. The development and production of isotope products unavailable or difficult to get commercially have been most recently the responsibility of the Department of Energy's Nuclear Energy program. The President's FY09 Budget request proposed the transfer of the Isotope Production program to the Department of Energy's Office of Science in Nuclear Physics and to rename it the National Isotope Production and Application program (NIPA). The transfer has now taken place with the signing of the 2009 appropriations bill. In preparation for this, the Nuclear Science Advisory Committee (NSAC) was requested to establish a standing subcommittee, the NSAC Isotope Subcommittee (NSACI), to advise the DOE Office of Nuclear Physics. The request came in the form of two charges: one, on setting research priorities in the short term for the most compelling opportunities from the vast array of disciplines that develop and use isotopes and two, on making a long term strategic plan for the NIPA program. This is the final report to address charge 1. NSACI membership is comprised of experts from the diverse research communities, industry, production, and homeland security. NSACI discussed research opportunities divided into three areas: (1) medicine, pharmaceuticals, and biology, (2) physical sciences and engineering, and (3) national security and other applications. In each area, compelling research opportunities were considered and the subcommittee as a whole determined the final priorities for research opportunities as the foundations for the recommendations. While it was challenging to prioritize across disciplines, our order of recommendations reflect the compelling research prioritization along with consideration of time urgency for action as well as various geopolitical market issues. Common observations to all areas of research include the needs for domestic availability of crucial stable and radioactive isotopes and the education of the skilled workforce that will develop new advances using isotopes in the future. The six recommendations of NSACI reflect these concerns and the compelling research opportunities for potential new discoveries. The science case for each of the recommendations is elaborated in the respective chapters.

None

2009-04-23T23:59:59.000Z

279

Kinetic Isotopic Fractionation During Diffusion of Ionic Speciesin Water  

Science Conference Proceedings (OSTI)

Experiments specifically designed to measure the ratio of the diffusivities of ions dissolved in water were used to determine D{sub Li}/D{sub K}, D{sub 7{sub Li}}/D{sub 6{sub Li}}, D{sub 25{sub Mg}}/D{sub 24{sub Mg}}, D{sub 26{sub Mg}}/D{sub 25{sub Mg}}, and D{sub 37{sub Cl}}/D{sub 35{sub Cl}}. The measured ratio of the diffusion coefficients for Li and K in water (D{sub Li}/D{sub K} = 0.6) is in good agreement with published data, providing evidence that the experimental design being used resolves the relative mobility of ions with adequate precision to also be used for determining the fractionation of isotopes by diffusion in water. In the case of Li we found measurable isotopic fractionation associated with the diffusion of dissolved LiCl (D{sub 7{sub Li}}/D{sub 6{sub Li}} = 0.99772 {+-} 0.00026). This difference in the diffusion coefficient of {sup 7}Li compared to {sup 6}Li is significantly less than reported in an earlier study, a difference we attribute to the fact that in the earlier study Li diffused through a membrane separating the water reservoirs. Our experiments involving Mg diffusing in water found no measurable isotopic fractionation (D{sub 25{sub Mg}}/D{sub 24{sub Mg}} = 1.00003 {+-} 0.00006). Cl isotopes were fractionated during diffusion in water (D{sub 37{sub Cl}}/D{sub 35{sub Cl}} = 0.99857 {+-} 0.00080) whether or not the co-diffuser (Li or Mg) was isotopically fractionated. The isotopic fractionation associated with the diffusion of ions in water is much smaller than values we found previously for the isotopic fractionation of Li and Ca isotopes by diffusion in molten silicate liquids. A major distinction between water and silicate liquids is that water, being a polar liquid, surrounds dissolved ions with hydration shells, which very likely play an important but still poorly understood role in reducing isotopic fractionation associated with diffusion.

Richter, Frank M.; Mendybaev, Ruslan A.; Christensen, John; Hutcheon, Ian D.; Williams, Ross W.; Sturchio, Neil C.; Beloso Jr.,Abelardo D.

2005-06-09T23:59:59.000Z

280

Laser Catalyst  

INL’s Laser Catalyst is a method for removing contaminant matter from a porous material. A polymer material is applied to a contaminated surface and ...

Note: This page contains sample records for the topic "laser isotope separation" 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

Copper Palladium Hydrogen Separation Membranes  

This patent-pending technology, “Cu-Pd Hydrogen Separation Membranes with Reduced Palladium Content and Improved Performance,” consists of copper-palladium alloy compositions for hydrogen separation membranes that use less palladium and have a ...

282

Separability of Tripartite Quantum Systems  

E-Print Network (OSTI)

We investigate the separability of arbitrary dimensional tripartite sys- tems. By introducing a new operator related to transformations on the subsystems a necessary condition for the separability of tripartite systems is presented.

Ming Li; Shao-Ming Fei; Zhi-Xi Wang

2008-09-05T23:59:59.000Z

283

Yuan Tseh Lee, 1981 | U.S. DOE Office of Science (SC)  

Office of Science (SC) Website

fundamental research contributions to chemical dynamics, with applications to laser dynamics and development, isotope separation, atmospheric chemistry, and contributions...

284

Isotopic Analysis- Rock | Open Energy Information  

Open Energy Info (EERE)

Isotopic Analysis- Rock Isotopic Analysis- Rock Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Technique: Isotopic Analysis- Rock Details Activities (13) Areas (11) Regions (0) NEPA(0) Exploration Technique Information Exploration Group: Lab Analysis Techniques Exploration Sub Group: Rock Lab Analysis Parent Exploration Technique: Rock Lab Analysis Information Provided by Technique Lithology: Water rock interaction Stratigraphic/Structural: Hydrological: Thermal: Dictionary.png Isotopic Analysis- Rock: Isotopes are atoms of the same element that have different numbers of neutrons. An isotopic analysis looks at a particular isotopic element(s) in a given system, while the conditions which increase/decrease the number of neutrons are well understood and measurable.

285

High-Resolution Separations Technologies  

Science Conference Proceedings (OSTI)

... gas chromatography mass spectrometry (GC/MS) provides relatively high efficiency separations, the analysis of some complex, natural-matrix ...

2012-10-09T23:59:59.000Z

286

Photoelectrochemical Separation and Imaging Device  

Disclosure Number 200301283 ... The invention relates to the separation and detection of biomolecules and other charged species using ...

287

Image separation using particle filters  

Science Conference Proceedings (OSTI)

In this work, we will analyze the problem of source separation in the case of superpositions of different source images, which need to be extracted from a set of noisy observations. This problem occurs, for example, in the field of astrophysics, where ... Keywords: Bayesian source separation, Image separation, Non-stationary noise, Particle filtering, Sequential Monte Carlo

Mauro Costagli; Ercan Engin Kuruo?lu

2007-09-01T23:59:59.000Z

288

HYDROGEN SEPARATION MEMBRANES  

DOE Green Energy (OSTI)

A likely membrane for future testing of high-temperature hydrogen separation from a gasification product stream was targeted as an inorganic analog of a dense-metal membrane, where the hydrogen would dissolve into and diffuse through the membrane structure. An amorphous membrane such as zinc sulfide appeared to be promising. Previously, ZnS film coating tests had been performed using an electron-beam vacuum coating instrument, with zinc films successfully applied to glass substrates. The coatings appeared relatively stable in air and in a simple simulated gasification atmosphere at elevated temperature. Because the electron-beam coating instrument suffered irreparable breakdown, several alternative methods were tested in an effort to produce a nitrogen-impermeable, hydrogen-permeable membrane on porous sintered steel substrates. None of the preparation methods proved successful in sealing the porous substrate against nitrogen gas. To provide a nitrogen-impermeable ZnS material to test for hydrogen permeability, two ZnS infrared sample windows were purchased. These relatively thick ''membranes'' did not show measurable permeation of hydrogen, either due to lack of absorption or a negligible permeation rate due to their thickness. To determine if hydrogen was indeed adsorbed, thermogravimetric and differential thermal analyses tests were performed on samples of ZnS powder. A significant uptake of hydrogen gas occurred, corresponding to a maximum of 1 mole H{sub 2} per 1 mole ZnS at a temperature of 175 C. The hydrogen remained in the material at ambient temperature in a hydrogen atmosphere, but approximately 50% would be removed in argon. Reheating in a hydrogen atmosphere resulted in no additional hydrogen uptake. Differential scanning calorimetry indicated that the hydrogen uptake was probably due to the formation of a zinc-sulfur-hydrogen species resulting in the formation of hydrogen sulfide. The zinc sulfide was found to be unstable above approximately 200 C, probably with the reduction to metallic zinc with the evolution of hydrogen sulfide. The work has shown that ZnS is not a viable candidate for a high-temperature hydrogen separation membrane.

Donald P. McCollor; John P. Kay

1999-08-01T23:59:59.000Z

289

NIST Laser Applications Group Homepage  

Science Conference Proceedings (OSTI)

Laser Applications Group. Welcome. The Laser Applications Group advances laser technology for applications in optical ...

2012-05-10T23:59:59.000Z

290

Studies in Photosynthesis with Isotopes  

E-Print Network (OSTI)

chlorophyll) SCHEMATIC DIAGRAM OF PHOTOSYNTHESIS Fig, P Fig.2 Time of photosynthesis 60c.f M U 1646 Fig. 5 Fig. 8 Fig. 94705-eng-48 STUDIES IN PHOTOSYNTHESIS WITH ISOTOPES M Calvin

Calvin, M.; Bassham, J.A.

1952-01-01T23:59:59.000Z

291

Laser beam guard clamps  

DOE Patents (OSTI)

A quick insert and release laser beam guard panel clamping apparatus having a base plate mountable on an optical table, a first jaw affixed to the base plate, and a spring-loaded second jaw slidably carried by the base plate to exert a clamping force. The first and second jaws each having a face acutely angled relative to the other face to form a V-shaped, open channel mouth, which enables wedge-action jaw separation by and subsequent clamping of a laser beam guard panel inserted through the open channel mouth. Preferably, the clamping apparatus also includes a support structure having an open slot aperture which is positioned over and parallel with the open channel mouth.

Dickson, Richard K. (Stockton, CA)

2010-09-07T23:59:59.000Z

292

RESONATOR PARTICLE SEPARATOR  

DOE Patents (OSTI)

A wave guide resonator structure is described for use in separating particles of equal momentum but differing in mass and having energies exceeding one billion electron volts. The particles are those of sub-atomic size and are generally produced as a result of the bombardment of a target by a beam such as protons produced in a high-energy accelerator. In this wave guide construction, the particles undergo preferential deflection as a result of the presence of an electric field. The boundary conditions established in the resonator are such as to eliminate an interfering magnetic component, and to otherwise phase the electric field to obtain a traveling wave such as one which moves at the same speed as the unwanted particle. The latter undergoes continuous deflection over the whole length of the device and is, therefore, eliminated while the wanted particle is deflected in opposite directions over the length of the resonator and is thus able to enter an exit aperture. (AEC)

Blewett, J.P.

1962-01-01T23:59:59.000Z

293

RESONATOR PARTICLE SEPARATOR  

DOE Patents (OSTI)

A wave-guide resonator structure is designed for use in separating particles of equal momentum but differing in mass, having energies exceeding one billion eiectron volts. The particles referred to are those of sub-atomic size and are generally produced as a result of the bombardment of a target by a beam such as protons produced in a high energy accelerator. In the resonator a travelling electric wave is produced which travels at the same rate of speed as the unwanted particle which is thus deflected continuously over the length of the resonator. The wanted particle is slightly out of phase with the travelling wave so that over the whole length of the resonator it has a net deflection of substantially zero. The travelling wave is established in a wave guide of rectangular cross section in which stubs are provided to store magnetic wave energy leaving the electric wave energy in the main structure to obtain the desired travelling wave and deflection. The stubs are of such shape and spacing to establish a critical mathemitical relationship. (AEC)

Blewett, J.P.; Kiesling, J.D.

1963-06-11T23:59:59.000Z

294

Metalworking Lasers  

Science Conference Proceedings (OSTI)

...Several models of metalworking lasers of both domestic and foreign manufacture are commercially available. The majority of these are of either the neodymium yttrium-aluminum garnet (Nd:YAG) solid-state type or the carbon dioxide (CO 2 ) gas type. These lasers may have pulsed or...

295

Laser device  

DOE Patents (OSTI)

A laser device includes a virtual source configured to aim laser energy that originates from a true source. The virtual source has a vertical rotational axis during vertical motion of the virtual source and the vertical axis passes through an exit point from which the laser energy emanates independent of virtual source position. The emanating laser energy is collinear with an orientation line. The laser device includes a virtual source manipulation mechanism that positions the virtual source. The manipulation mechanism has a center of lateral pivot approximately coincident with a lateral index and a center of vertical pivot approximately coincident with a vertical index. The vertical index and lateral index intersect at an index origin. The virtual source and manipulation mechanism auto align the orientation line through the index origin during virtual source motion.

Scott, Jill R. (Idaho Falls, ID); Tremblay, Paul L. (Idaho Falls, ID)

2008-08-19T23:59:59.000Z

296

Ultrashort pulse laser deposition of thin films  

DOE Patents (OSTI)

Short pulse PLD is a viable technique of producing high quality films with properties very close to that of crystalline diamond. The plasma generated using femtosecond lasers is composed of single atom ions with no clusters producing films with high Sp.sup.3 /Sp.sup.2 ratios. Using a high average power femtosecond laser system, the present invention dramatically increases deposition rates to up to 25 .mu.m/hr (which exceeds many CVD processes) while growing particulate-free films. In the present invention, deposition rates is a function of laser wavelength, laser fluence, laser spot size, and target/substrate separation. The relevant laser parameters are shown to ensure particulate-free growth, and characterizations of the films grown are made using several diagnostic techniques including electron energy loss spectroscopy (EELS) and Raman spectroscopy.

Perry, Michael D. (Livermore, CA); Banks, Paul S. (Livermore, CA); Stuart, Brent C. (Fremont, CA)

2002-01-01T23:59:59.000Z

297

Global Laser Enrichment  

E-Print Network (OSTI)

APPLICATION – PUBLIC RESPONSES GE-Hitachi Global Laser Enrichment LLC (GLE) hereby submits the additional information requested in the November 19, 2009 letter. Enclosure 1 of this letter contains the responses the questions. A separate letter has been submitted that contains a non-public version of these responses, which contains Export-Controlled and Security-Related Information. If there are any questions regarding this letter and its contents, please do not hesitate to contact myself, or Julie Olivier of my staff at 910-819-4799 or at Julie.Olivier@ge.com.

Uranium Enrichment Branch; Albert E. Kennedy; Albert E. Kennedy; Tammy Orr (gle

2009-01-01T23:59:59.000Z

298

Global Laser Enrichment  

E-Print Network (OSTI)

PUBLIC VERSION GE-Hitachi Global Laser Enrichment LLC (GLE) hereby submits revision 2 of the GLE License Application. Enclosure 1 contains revised Request for Additional Information responses. Enclosure 2 contains revised chapters 1, 2, 3, 5, 7, and 11 of the GLE License Application. Enclosure 3 contains the revised pubic version of the Decommissioning Funding Plan. Non-Public versions of the revised License Application and the Decommissioning Funding Plan have been prepared and will be submitted under separate enclosure. If there are any questions regarding this letter and its contents, please do not hesitate to contact me at 910-819-4799 or at

Julie Olivier; Brian Smith Chief; Uranium Enrichment Branch; Julie Olivier; Tim Johnson (nrc; Tammy Orr (gle; Lori Butler (geh; Jerry Head (geh; Patricia Campbell (geh; Bob Crate (gle; Ken Givens (gle; Tom Owens (gle

2010-01-01T23:59:59.000Z

299

Isotope production facility produces cancer-fighting actinium  

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

Cancer therapy gets a boost from new isotope Isotope production facility produces cancer-fighting actinium A new medical isotope project shows promise for rapidly producing major...

300

Measurement of the separation between atoms beyond diffraction limit  

E-Print Network (OSTI)

Precision measurement of small separations between two atoms or molecules has been of interest since the early days of science. Here, we discuss a scheme which yields spatial information on a system of two identical atoms placed in a standing wave laser field. The information is extracted from the collective resonance fluorescence spectrum, relying entirely on far-field imaging techniques. Both the interatomic separation and the positions of the two particles can be measured with fractional-wavelength precision over a wide range of distances from bout lambda/550 to lambda/2.

Jun-Tao Chang; Joerg Evers; Marlan O. Scully; M. Suhail Zubairy

2005-08-01T23:59:59.000Z

Note: This page contains sample records for the topic "laser isotope separation" 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

Definition: Isotopic Analysis- Fluid | Open Energy Information  

Open Energy Info (EERE)

Definition Definition Edit with form History Facebook icon Twitter icon » Definition: Isotopic Analysis- Fluid Jump to: navigation, search Dictionary.png Isotopic Analysis- Fluid Isotopes are atoms of the same element that have different numbers of neutrons. An isotopic analysis looks at a particular isotopic element(s) in a given system, while the conditions which increase/decrease the number of neutrons are well understood and measurable. Fluid isotopes are used to characterize a fluids origin, age, and/or interaction with rocks or other fluids based on unique isotopic ratios or concentrations.[1] View on Wikipedia Wikipedia Definition Isotope geochemistry is an aspect of geology based upon study of the relative and absolute concentrations of the elements and their isotopes in

302

Isotopic generator for bismuth-212 and lead-212 from radium  

DOE Patents (OSTI)

A method and apparatus for providing radionuclides of bismuth-212 and lead-212. Thorium-228 and carrier solution starting material is input to a radiologically contained portion of an isotopic generator system, and radium-224 is separated from thorium-228 which is retained by a strongly basic anion exchange column. The separated radium-224 is transferred to an accessible, strongly acidic cationic exchange column. The cationic column retains the radium-224, and natural radioactive decay generates bismuth-212 and lead-212. The cationic exchange column can also be separated from the contained portion of the system and utilized without the extraordinary safety measures necessary in the contained portion. Furthermore, the cationic exchange column provides over a relatively long time period the short lived lead-212 and bismuth-212 radionuclides which are useful for a variety of medical therapies.

Atcher, Robert W. (Kensington, MD); Friedman, Arnold M. (Park Forest, IL); Hines, John (Glen Ellyn, IL)

1987-01-01T23:59:59.000Z

303

Laser Beams  

E-Print Network (OSTI)

• Community needs to work together to provide the technical case for funding an IFE program. • IFE program should nurture competition, with judgments made on the basis of technical progress and the potential of the various approaches to IFE. • Direct-drive with lasers looks very attractive for IFE, the physics and needed technologies are mature and advancing. • KrF provides physics advantages for direct drive. • KrF’s demonstrated performance is competitive with solid state lasers as a high-rep-rate durable, efficient IFE driver. (on several important parameters KrF technology leads) Direct Laser Drive is a better choice for Energy

Steve Obenschain

2010-01-01T23:59:59.000Z

304

Gas laser  

SciTech Connect

According to the invention, the gas laser comprises a housing which accommodates two electrodes. One of the electrodes is sectional and has a ballast resistor connected to each section. One of the electrodes is so secured in the housing that it is possible to vary the spacing between the electrodes in the direction of the flow of a gas mixture passed through an active zone between the electrodes where the laser effect is produced. The invention provides for a maximum efficiency of the laser under different operating conditions.

Kosyrev, F. K.; Leonov, A. P.; Pekh, A. K.; Timofeev, V. A.

1980-08-12T23:59:59.000Z

305

Gas separation membrane module assembly  

SciTech Connect

A gas-separation membrane module assembly and a gas-separation process using the assembly. The assembly includes a set of tubes, each containing gas-separation membranes, arranged within a housing. The housing contains a tube sheet that divides the space within the housing into two gas-tight spaces. A permeate collection system within the housing gathers permeate gas from the tubes for discharge from the housing.

Wynn, Nicholas P (Palo Alto, CA); Fulton, Donald A. (Fairfield, CA)

2009-03-31T23:59:59.000Z

306

Process for recovering evolved hydrogen enriched with at least one heavy hydrogen isotope  

DOE Patents (OSTI)

This invention relates to a separation means and method for enriching a hydrogen atmosphere with at least one heavy hydrogen isotope by using a solid titaniun alloy hydride. To this end, the titanium alloy hydride containing at least one metal selected from the group consisting of vanadium, chromium, manganese, molybdenum, iron, cobalt and nickel is contacted with a circulating gaseous flow of hydrogen containing at least one heavy hydrogen isotope at a temperature in the range of -20.degree. to +40.degree. C and at a pressure above the dissociation pressure of the hydrided alloy selectively to concentrate at least one of the isotopes of hydrogen in the hydrided metal alloy. The contacting is continued until equilibrium is reached, and then the gaseous flow is isolated while the temperature and pressure of the enriched hydride remain undisturbed selectively to isolate the hydride. Thereafter, the enriched hydrogen is selectively recovered in accordance with the separation factor (S.F.) of the alloy hydride employed.

Tanaka, John (Storrs, CT); Reilly, Jr., James J. (Bellport, NY)

1978-01-01T23:59:59.000Z

307

Separate Training Influences Relative Validity  

E-Print Network (OSTI)

concurrent inhibitory training of B were to alter respondingComparative Psychology Separate Training Influences RelativeDuring relative validity training, X was reinforced when

Mehta, Rick; Dumont, Jamie-Lynne; Combiadakis, Sharon; Williams, Douglas A.

2004-01-01T23:59:59.000Z

308

Laser Program annual report, 1985  

Science Conference Proceedings (OSTI)

This volume presents the unclassified activities and accomplishments of the Inertial Confinement Fusion and Advanced Laser Development elements of the Laser Program at the Lawrence Livermore National Laboratory for the calendar year 1985. This report has been organized into major sections that correspond to our principal technical activities. Section 1 provides an overview. Section 2 comprises work in target theory, design, and code development. Target development and fabrication and the related topics in materials science are contained in Section 3. Section 4 presents work in experiments and diagnostics and includes developments in data acquisition and management capabilities. In Section 5 laser system (Nova) operation and maintenance are discussed. Activities related to supporting laser and optical technologies are described in Section 6. Basic laser research and development is reported in Section 7. Section 8 contains the results of studies in ICF applications where the work reported deals principally with the production of electric power with ICF. Finally, Section 9 is a comprehensive discussion of work to date on solid state lasers for average power applications. Individual sections, two through nine, have been cataloged separately.

Rufer, M.L.; Murphy, P.W. (eds.)

1986-11-01T23:59:59.000Z

309

Laser barometer  

DOE Patents (OSTI)

This paper describes an invention of a pressure measuring instrument which uses laser radiation to sense the pressure in an enclosed environment by means of measuring the change in refractive index of a gas - which is pressure dependent.

Abercrombie, K.R.; Shiels, D.; Rash, T.

1998-04-01T23:59:59.000Z

310

Studies of phase separable soluble polymers  

E-Print Network (OSTI)

The technique of phase labeling has the ability to greatly enhance synthetic protocol by simplifying purification and increasing efficiency. Traditional insoluble supports offer efficient and simple recovery of the Â?phase taggedÂ? material but suffer from problems inherent to their heterogeneous nature. A solution to these problems has been to utilize phase separable soluble polymers in the design of Â?smartÂ? responsive systems that offer the option of homogenous reaction conditions with heterogeneous separation conditions. The subject of this dissertation focuses on the application of soluble polymeric phase tags in systems where the miscibility between solid-liquid and liquid-liquid systems is thermally induced. Low molecular weight poly(ethylene glycol) (PEG) oligomers were investigated as phase anchors for SCS palladacycle catalysts. The oligomeric PEG chains were sufficient to engender polar phase solubility in a heptane-DMA thermomorphic system. Microwave irradiation of these thermomorphic mixtures of palladium complexes and substrates was a viable scheme to recycle and significantly shorten reaction times for simple Heck reactions of aryl iodides. Soluble polymeric supports possessing a lower critical solution temperature (LCST) were utilized in the sequestration of the S-triazine herbicide, atrazine, from contaminated water samples. The ability of poly(N-isopropylacrylamide) to sequester hydrophobic guests like atrazine was examined. A functionalized PNIPAM derivative containing secondary cyclic amines exhibited superior sequestration ability that was credited to the covalent binding of the atrazine. In order to facilitate the design of tailored, thermally responsive, smart polymers, a high throughput temperature gradient microfluidic device was used to obtain LCST data in a fast, accurate manner. The specific ion effects of various alkali metal halide salts on the LCST of PNIPAM were investigated. The high precision in the measurements enabled more subtle effects such as changes in solvent isotope, polymer microstructure, molecular weight, and importance of end group effects on the LCST of poly(N-alkylacrylamide)s to be evaluated.

Furyk, Steven Michael

2003-05-01T23:59:59.000Z

311

Coherence delay augmented laser beam homogenizer  

SciTech Connect

The geometrical restrictions on a laser beam homogenizer are relaxed by ug a coherence delay line to separate a coherent input beam into several components each having a path length difference equal to a multiple of the coherence length with respect to the other components. The components recombine incoherently at the output of the homogenizer, and the resultant beam has a more uniform spatial intensity suitable for microlithography and laser pantogography. Also disclosed is a variable aperture homogenizer, and a liquid filled homogenizer.

Rasmussen, Paul (Livermore, CA); Bernhardt, Anthony (Berkeley, CA)

1993-01-01T23:59:59.000Z

312

Separator material for electrochemical cells  

DOE Patents (OSTI)

An electrochemical cell is characterized as utilizing an aramid fiber as a separator material. The aramid fibers are especially suited for lithium/thionyl chloride battery systems. The battery separator made of aramid fibers possesses superior mechanical strength, chemical resistance, and is flame retardant.

Cieslak, W.R.; Storz, L.J.

1991-03-26T23:59:59.000Z

313

Separator material for electrochemical cells  

DOE Patents (OSTI)

An electrochemical cell characterized as utilizing an aramid fiber as a separator material. The aramid fibers are especially suited for lithium/thionyl chloride battery systems. The battery separator made of aramid fibers possesses superior mechanical strength, chemical resistance, and is flame retardant. 1 tab.

Cieslak, W.R.; Storz, L.J.

1989-06-12T23:59:59.000Z

314

Three phase downhole separator process  

DOE Patents (OSTI)

Three Phase Downhole Separator Process (TPDSP) is a process which results in the separation of all three phases, (1) oil, (2) gas, and (3) water, at the downhole location in the well bore, water disposal injection downhole, and oil and gas production uphole.

Cognata, Louis John (Baytown, TX)

2008-06-24T23:59:59.000Z

315

Set separation Neural Network paradigms  

E-Print Network (OSTI)

for forecasting financial time series 29 f´evrier 2008 Designing a neural network for forecasting financial time for forecasting financial time series #12;Neural Net The inputs Set separation Neural Network paradigms From network for forecasting financial time series #12;Neural Net The inputs Set separation Neural Network

Chen, Yiling

316

Separator material for electrochemical cells  

DOE Patents (OSTI)

An electrochemical cell characterized as utilizing an aramid fiber as a separator material. The aramid fibers are especially suited for lithium/thionyl chloride battery systems. The battery separator made of aramid fibers possesses superior mechanical strength, chemical resistance, and is flame retardant.

Cieslak, Wendy R. (1166 Laurel Loop NE., Albuquerque, NM 87122); Storz, Leonard J. (2215 Ambassador NE., Albuquerque, NM 87112)

1991-01-01T23:59:59.000Z

317

Hydrogen separation using silica membranes  

Science Conference Proceedings (OSTI)

Silica membranes were synthesized on tubular supports of alumina by dipping in silica colloidal solutions. The quality and the performance of the silica membranes were tested by experiments on single gas permeation and gas separation of mixed N2, ... Keywords: Knudsen diffusion, colloidal solution, gas permeation, hydrogen separation, silica membranes

Salvador Alfaroa; Miguel A. Valenzuelaa; Pedro Bosch

2008-11-01T23:59:59.000Z

318

METHOD OF SEPARATING URANIUM SUSPENSIONS  

DOE Patents (OSTI)

A process is presented for separating colloidally dissed uranium oxides from the heavy water medium in upwhich they are contained. The method consists in treating such dispersions with hydrogen peroxide, thereby converting the uranium to non-colloidal UO/sub 4/, and separating the UO/sub 4/ sfter its rapid settling.

Wigner, E.P.; McAdams, W.A.

1958-08-26T23:59:59.000Z

319

Low Cost Geothermal Separators BLISS Boundary Layer Inline Separator Scrubber  

DOE Green Energy (OSTI)

A new compact, low cost, and high performance separator is being developed to help reduce the installed and O and M cost of geothermal power generation. This device has been given the acronym ''BLISS'' that stands for ''Boundary Layer Inline Separator Scrubber''. The device is the first of a series of separators, and in the case of injectates, scrubbers to address the cost-reduction needs of the industry. The BLISS is a multi-positional centrifugal separator primarily designed to be simply installed between pipe supports, in a horizontal position. This lower profile reduces the height safety concern for workers, and significantly reduces the total installation cost. The vessel can demand as little as one-quarter (25%) the amount of steel traditionally required to fabricate many large vertical separators. The compact nature and high separating efficiency of this device are directly attributable to a high centrifugal force coupled with boundary layer control. The pseudo isokinetic flow design imparts a self-cleaning and scale resistant feature. This polishing separator is designed to remove moderate amounts of liquid and entrained solids.

Jung, Douglas; Wai, King

2000-05-26T23:59:59.000Z

320

It's Elemental - Isotopes of the Element Mendelevium  

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

The Periodic Table of Elements Next Element (Nobelium) Nobelium Isotopes of the Element Mendelevium Click for Main Data Most of the isotope data on this site has been obtained...

Note: This page contains sample records for the topic "laser isotope separation" 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

It's Elemental - Isotopes of the Element Uranium  

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

Periodic Table of Elements Next Element (Neptunium) Neptunium Isotopes of the Element Uranium Click for Main Data Most of the isotope data on this site has been obtained from...

322

It's Elemental - Isotopes of the Element Lithium  

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

Periodic Table of Elements Next Element (Beryllium) Beryllium Isotopes of the Element Lithium Click for Main Data Most of the isotope data on this site has been obtained from...

323

It's Elemental - Isotopes of the Element Hydrogen  

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

The Periodic Table of Elements Next Element (Helium) Helium Isotopes of the Element Hydrogen Click for Main Data Most of the isotope data on this site has been obtained from...

324

Isotope GeoloGy1 Unlike physics or chemistry, teaching isotope  

E-Print Network (OSTI)

Isotope GeoloGy1 Unlike physics or chemistry, teaching isotope geochemistry is difficult because. Writing an effective book on geochemistry is thus even more difficult. Claude Allègre's Isotope Geology geochemistry book, given how effective the texts by Faure and Dickin are. However, Allègre's Isotope Geology

Lee, Cin-Ty Aeolus

325

ISOTOPE FRACTIONATION Isotopes are atoms whose nuclei contain the same number of protons but a different number of neutrons. The  

E-Print Network (OSTI)

for the utilization of stable isotopes in geology, geochemistry, biogeochemistry, paleoceanography and elsewhere____________________________ ISOTOPE FRACTIONATION ____________________________ Isotopes are atoms whose nuclei contain the same number of protons but a different number of neutrons. The term `isotope

Zeebe, Richard E.

326

Isotopic Abundance in Atom Trap Trace Analysis  

isotopes for climate change and nuclear proliferation interests. The Invention Argonne scientists have created a novel method and system for

327

Study of Laser Scintillation in Different Atmospheric Conditions  

Science Conference Proceedings (OSTI)

Laser scintillation observations were carried out over a flat surface in different atmospheric conditions on 33 separate days during March 1990?April 1991 and were analyzed and studied. The principal results of the analysis reveal (i) marked ...

P. Ernest Raj; S. Sharma; P. C. S. Devara; G. Pandithurai

1993-06-01T23:59:59.000Z

328

Vacuum barrier for excimer lasers  

DOE Patents (OSTI)

This invention is comprised of a barrier for separating the vacuum area of a diode from the pressurized gas area of an excimer laser. The barrier is a composite material comprising layers of a metal such as copper, along with layers of polyimide, and a matrix of graphite fiber yearns impregnated with epoxy. The barrier is stronger than conventional foil barriers, and allows greater electron throughput.

Shurter, R.P.

1990-10-10T23:59:59.000Z

329

"Environmental Isotope Geochemistry": Past, Present Mark Baskaran  

E-Print Network (OSTI)

Chapter 1 "Environmental Isotope Geochemistry": Past, Present and Future Mark Baskaran 1.1 Introduction and Early History A large number of radioactive and stable isotopes of the first 95 elements unraveling many secrets of our Earth and its environmental health. These isotopes, because of their suitable

Baskaran, Mark

330

Dual wavelength laser damage testing for high energy lasers.  

Science Conference Proceedings (OSTI)

As high energy laser systems evolve towards higher energies, fundamental material properties such as the laser-induced damage threshold (LIDT) of the optics limit the overall system performance. The Z-Backlighter Laser Facility at Sandia National Laboratories uses a pair of such kiljoule-class Nd:Phosphate Glass lasers for x-ray radiography of high energy density physics events on the Z-Accelerator. These two systems, the Z-Beamlet system operating at 527nm/ 1ns and the Z-Petawatt system operating at 1054nm/ 0.5ps, can be combined for some experimental applications. In these scenarios, dichroic beam combining optics and subsequent dual wavelength high reflectors will see a high fluence from combined simultaneous laser exposure and may even see lingering effects when used for pump-probe configurations. Only recently have researchers begun to explore such concerns, looking at individual and simultaneous exposures of optics to 1064 and third harmonic 355nm light from Nd:YAG [1]. However, to our knowledge, measurements of simultaneous and delayed dual wavelength damage thresholds on such optics have not been performed for exposure to 1054nm and its second harmonic light, especially when the pulses are of disparate pulse duration. The Z-Backlighter Facility has an instrumented damage tester setup to examine the issues of laser-induced damage thresholds in a variety of such situations [2] . Using this damage tester, we have measured the LIDT of dual wavelength high reflectors at 1054nm/0.5ps and 532nm/7ns, separately and spatially combined, both co-temporal and delayed, with single and multiple exposures. We found that the LIDT of the sample at 1054nm/0.5ps can be significantly lowered, from 1.32J/cm{sup 2} damage fluence with 1054/0.5ps only to 1.05 J/cm{sup 2} with the simultaneous presence of 532nm/7ns laser light at a fluence of 8.1 J/cm{sup 2}. This reduction of LIDT of the sample at 1054nm/0.5ps continues as the fluence of 532nm/7ns laser light simultaneously present increases. The reduction of LIDT does not occur when the 2 pulses are temporally separated. This paper will also present dual wavelength LIDT results of commercial dichroic beam-combining optics simultaneously exposed with laser light at 1054nm/2.5ns and 532nm/7ns.

Atherton, Briggs W.; Rambo, Patrick K.; Schwarz, Jens; Kimmel, Mark W.

2010-05-01T23:59:59.000Z

331

laser_measurements  

Science Conference Proceedings (OSTI)

Dimensional Measurements. Laser Measurements. Rate our Services. Technical ... Laser Frequency/Wavelength (14510S-14511S). The ...

2013-04-09T23:59:59.000Z

332

Radioactive isotopes on the Moon  

SciTech Connect

A limited review of experiments and studies of radioactivity and isotope ratios in lunar materials is given. Observations made on the first few millimeters of the surface where the effects of solar flare particles are important, some measurements on individual rocks, and some studies of radioactivities produced deep in the lunar soil by galactic cosmic rays, are among the experiments discussed. (GHT)

Davis, R. Jr.

1975-01-01T23:59:59.000Z

333

Methane/nitrogen separation process  

DOE Patents (OSTI)

A membrane separation process for treating a gas stream containing methane and nitrogen, for example, natural gas. The separation process works by preferentially permeating methane and rejecting nitrogen. We have found that the process is able to meet natural gas pipeline specifications for nitrogen, with acceptably small methane loss, so long as the membrane can exhibit a methane/nitrogen selectivity of about 4, 5 or more. This selectivity can be achieved with some rubbery and super-glassy membranes at low temperatures. The process can also be used for separating ethylene from nitrogen.

Baker, Richard W. (Palo Alto, CA); Lokhandwala, Kaaeid A. (Menlo Park, CA); Pinnau, Ingo (Palo Alto, CA); Segelke, Scott (Mountain View, CA)

1997-01-01T23:59:59.000Z

334

Methane/nitrogen separation process  

DOE Patents (OSTI)

A membrane separation process is described for treating a gas stream containing methane and nitrogen, for example, natural gas. The separation process works by preferentially permeating methane and rejecting nitrogen. The authors have found that the process is able to meet natural gas pipeline specifications for nitrogen, with acceptably small methane loss, so long as the membrane can exhibit a methane/nitrogen selectivity of about 4, 5 or more. This selectivity can be achieved with some rubbery and super-glassy membranes at low temperatures. The process can also be used for separating ethylene from nitrogen. 11 figs.

Baker, R.W.; Lokhandwala, K.A.; Pinnau, I.; Segelke, S.

1997-09-23T23:59:59.000Z

335

Efficient separations & processing crosscutting program  

Science Conference Proceedings (OSTI)

The Efficient Separations and Processing Crosscutting Program (ESP) was created in 1991 to identify, develop, and perfect chemical and physical separations technologies and chemical processes which treat wastes and address environmental problems throughout the DOE complex. The ESP funds several multiyear tasks that address high-priority waste remediation problems involving high-level, low-level, transuranic, hazardous, and mixed (radioactive and hazardous) wastes. The ESP supports applied research and development (R & D) leading to the demonstration or use of these separations technologies by other organizations within the Department of Energy (DOE), Office of Environmental Management.

NONE

1996-08-01T23:59:59.000Z

336

Lasers and Optoelectronic Components Used with Lasers  

Science Conference Proceedings (OSTI)

... example, beam profile and relative intensity noise ... for the laser wavelengths and energies for which ... The laser power and energy measurements are ...

2013-06-28T23:59:59.000Z

337

Laser Beam Delivery [Laser Applications Laboratory] - Nuclear...  

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

Laser Glazing of Railroad Rails High Power Laser Beam Delivery Decontamination and Decommissioning Refractory Alloy Welding Robots Applications Other Facilities Other Capabilities...

338

Slag capture and removal during laser cutting. [Patent application  

DOE Patents (OSTI)

Molten metal removed from a workpiece in a laser cutting operation is blown away from the cutting point by a gas jet and collected on an electromagnet. The laser cutting is used to separate the castings of spent fuel rods from the fuel-containing elements therein.

Brown, C.O.

1982-01-28T23:59:59.000Z

339

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

340

Device for separating a mixture  

SciTech Connect

A device is described for separating a mixture of, for example, oil and water consists of a number of elements treating the mixture in stages, said elements being arranged in overlying position in order to manufacture a compact device.

Koot, T.A.; Verpalen, W.A.

1981-05-05T23:59:59.000Z

Note: This page contains sample records for the topic "laser isotope separation" 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

Laser barometer  

DOE Patents (OSTI)

A pressure measuring instrument that utilizes the change of the refractive index of a gas as a function of pressure and the coherent nature of a laser light to determine the barometric pressure within an environment. As the gas pressure in a closed environment varies, the index of refraction of the gas changes. The amount of change is a function of the gas pressure. By illuminating the gas with a laser light source, causing the wavelength of the light to change, pressure can be quantified by measuring the shift in fringes (alternating light and dark bands produced when coherent light is mixed) in an interferometer.

Abercrombie, Kevin R. (Westminster, CO); Shiels, David (Thornton, CO); Rash, Tim (Aurora, CO)

2001-02-06T23:59:59.000Z

342

Entanglement transformations using separable operations  

E-Print Network (OSTI)

We study conditions for the deterministic transformation $\\ket{\\psi}\\longrightarrow\\ket{\\phi}$ of a bipartite entangled state by a separable operation. If the separable operation is a local operation with classical communication (LOCC), Nielsen's majorization theorem provides necessary and sufficient conditions. For the general case we derive a necessary condition in terms of products of Schmidt coefficients, which is equivalent to the Nielsen condition when either of the two factor spaces is of dimension 2, but is otherwise weaker. One implication is that no separable operation can reverse a deterministic map produced by another separable operation, if one excludes the case where the Schmidt coefficients of $\\ket{\\psi}$ and are the same as those of $\\ket{\\phi}$. The question of sufficient conditions in the general separable case remains open. When the Schmidt coefficients of $\\ket{\\psi}$ are the same as those of $\\ket{\\phi}$, we show that the Kraus operators of the separable transformation restricted to the supports of $\\ket{\\psi}$ on the factor spaces are proportional to unitaries. When that proportionality holds and the factor spaces have equal dimension, we find conditions for the deterministic transformation of a collection of several full Schmidt rank pure states $\\ket{\\psi_j}$ to pure states $\\ket{\\phi_j}$.

Vlad Gheorghiu; Robert B. Griffiths

2007-05-02T23:59:59.000Z

343

Definition: Isotopic Analysis- Rock | Open Energy Information  

Open Energy Info (EERE)

Isotopic Analysis- Rock Isotopic Analysis- Rock Jump to: navigation, search Dictionary.png Isotopic Analysis- Rock Isotopes are atoms of the same element that have different numbers of neutrons. An isotopic analysis looks at a particular isotopic element(s) in a given system, while the conditions which increase/decrease the number of neutrons are well understood and measurable.[1] View on Wikipedia Wikipedia Definition References ↑ http://wwwrcamnl.wr.usgs.gov/isoig/isopubs/itchch2.html Ret LikeLike UnlikeLike You like this.Sign Up to see what your friends like. rieved from "http://en.openei.org/w/index.php?title=Definition:Isotopic_Analysis-_Rock&oldid=687702" Category: Definitions What links here Related changes Special pages Printable version Permanent link Browse properties

344

Ultrasensitive detection of radioactive cesium isotopes using a magneto-optical trap.  

SciTech Connect

We report the first magneto-optical trapping of mdioactive {sup 135}Cs and {sup 137}Cs and a promising means for detecting these isotopes to ullrasensilive lcvels by a system coupling the magneto-optical trap (MOT) to a mass separator. The mass separator efficiently delivers a 20 kV ion beam of either isotope into a quartzcube MOT cell having in one corner a small-diameter Zr foil, on which the ion beam is focused and into which the ions are implantetl. Inductive heating of thc foil releases {approx}45% of the implanted atoms into a MOT that uses large diameter beams and a dry-film coating to capture 3% of the released vapor. MOT fluorescence signals were found to increasc linearly with the number of foil-implanted atoms over a range of 10{sup 4} to 10{sup 7} in trapped-atom number. The measured slope of MOT signal versus number implanted was equal in the case each isotope to within 4%, signifying our ability to measure {sup 137}Cs/{sup 135}Cs ratios to within 4%. The isotopic selectivities of the mass separator and MOT combine to suppress interfering signal from {sup 133}Cs by a factor of greater than 5 x 10{sup 12} in the case of detecting {sup 135}Cs or {sup 137}Cs. Our present sample detection sensitivity is one million atoms.

Di Rosa, M. D. (Michael D.); Crane, S. G. (Scott G.); Kitten, J. J. (Jason J.); Taylor, W. A. (Wayne A.); Vieira, D. J. (David J.); Zhao, X. (Xinxin)

2002-01-01T23:59:59.000Z

345

Laser wavelength effects in ultrafast near-field laser nanostructuring...  

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

Laser wavelength effects in ultrafast near-field laser nanostructuring of Si Title Laser wavelength effects in ultrafast near-field laser nanostructuring of Si Publication Type...

346

EA-1655: Berkeley Lab Laser Accelerator (BELLA) Laser Acquisition...  

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

655: Berkeley Lab Laser Accelerator (BELLA) Laser Acquisition, Installation and Use for Research and Development EA-1655: Berkeley Lab Laser Accelerator (BELLA) Laser Acquisition,...

347

Separation  

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

the same amount of electricity or more. Power generation with nuclear and renewable energy, such as wind, solar, geo- thermal, tidal, and hydroelectric, must be expanded as...

348

Isotopes Tell Origin and Operation of the Sun  

E-Print Network (OSTI)

The Iron Sun formed on the collapsed core of a supernova and now acts as a magnetic plasma diffuser, as did the precursor star, separating ions by mass. This process covers the solar surface with lightweight elements and with lighter isotopes of each element. Running difference images expose rigid, iron-rich structures below the fluid photosphere made of lightweight elements. The energy source for the Sun and ordinary stars seems to be neutron-emission and neutron-decay, with partial fusion of the decay product, rather than simple fusion of hydrogen into helium or heavier elements. Neutron-emission from the solar core and neutron-decay generate about sixty five percent of solar luminosity and H-fusion generates about thirty-five percent. The upward flow of H ions maintains mass-separation in the Sun. Only about one percent of this neutron decay product survives its upward journey to depart as solar-wind hydrogen.

O. Manuel; Sumeet A. Kamat; Michael Mozina

2005-09-28T23:59:59.000Z

349

Measurement of Trace Uranium Isotopes  

Science Conference Proceedings (OSTI)

The extent to which thermal ionization mass spectrometry (TIMS) can measure trace quantities of 233U and 236U in the presence of a huge excess of natural uranium is evaluated. This is an important nuclear non-proliferation measurement. Four ion production methods were evaluated with three mass spectrometer combinations. The most favorable combinations are not limited by abundance sensitivity; rather, the limitations are the ability to generate a uranium ion beam of sufficient intensity to obtain the required number of counts on the minor isotopes in relationship to detector background. The most favorable situations can measure isotope ratios in the range of E10 if sufficient sample intensity is available. These are the triple sector mass spectrometer with porous ion emitters (PIE) and the single sector mass spectrometer with energy filtering.

Matthew G. Watrous; James E. Delmore

2011-05-01T23:59:59.000Z

350

Molten carbonate fuel cell separator  

DOE Patents (OSTI)

In a stacked array of molten carbonate fuel cells, a fuel cell separator is positioned between adjacent fuel cells to provide isolation as well as a conductive path therebetween. The center portion of the fuel cell separator includes a generally rectangular, flat, electrical conductor. Around the periphery of the flat portion of the separator are positioned a plurality of elongated resilient flanges which form a gas-tight seal around the edges of the fuel cell. With one elongated flange resiliently engaging a respective edge of the center portion of the separator, the sealing flanges, which are preferably comprised of a noncorrosive material such as an alloy of yttrium, iron, aluminum or chromium, form a tight-fitting wet seal for confining the corrosive elements of the fuel cell therein. This arrangement permits a good conductive material which may be highly subject to corrosion and dissolution to be used in combination with a corrosion-resistant material in the fuel cell separator of a molten carbonate fuel cell for improved fuel cell conductivity and a gas-tight wet seal.

Nickols, Richard C. (East Hartford, CT)

1986-09-02T23:59:59.000Z

351

Molten carbonate fuel cell separator  

DOE Patents (OSTI)

In a stacked array of molten carbonate fuel cells, a fuel cell separator is positioned between adjacent fuel cells to provide isolation as well as a conductive path therebetween. The center portion of the fuel cell separator includes a generally rectangular, flat, electrical conductor. Around the periphery of the flat portion of the separator are positioned a plurality of elongated resilient flanges which form a gas-tight seal around the edges of the fuel cell. With one elongated flange resiliently engaging a respective edge of the center portion of the separator, the sealing flanges, which are preferably comprised of a noncorrosive material such as an alloy of yttrium, iron, aluminum or chromium, form a tight-fitting wet seal for confining the corrosive elements of the fuel cell therein. This arrangement permits a good conductive material which may be highly subject to corrosion and dissolution to be used in combination with a corrosion-resistant material in the fuel cell separator of a molten carbonate fuel cell for improved fuel cell conductivity and a gas-tight wet seal.

Nickols, R.C.

1984-10-17T23:59:59.000Z

352

Apparatus for molecular weight separation  

DOE Patents (OSTI)

The present invention relates generally to an apparatus and method for separating high molecular weight molecules from low molecular weight molecules. More specifically, the invention relates to the use of microdialysis for removal of the salt (low molecular weight molecules) from a nucleotide sample (high molecular weight molecules) for ESI-MS analysis. The dialysis or separation performance of the present invention is improved by (1) increasing dialysis temperature thereby increasing desalting efficiency and improving spectrum quality; (2) adding piperidine and imidazole to the dialysis buffer solution and reducing charge states and further increasing detection sensitivity for DNA; (3) using low concentrations (0-2.5 mM NH4OAc) of dialysis buffer and shifting the DNA negative ions to higher charge states, producing a nearly 10-fold increase in detection sensitivity and a slightly decreased desalting efficiency, (4) conducting a two-stage separation or (5) any combination of (1), (2), (3) and (4).

Smith, Richard D. (Richland, WA); Liu, Chuanliang (Haverhill, MA)

2001-01-01T23:59:59.000Z

353

Efficient laser amplifier using sequential pulses of different wavelengths  

SciTech Connect

A laser oscillator output pulse is separated into a plurality of separate beams which are temporally or spatially individually amplified by a power amplifier. The beams may then be recombined to provide a more powerful output than conventional single beam amplification.

Stark, Jr., Eugene E. (Los Alamos, NM); Kephart, John F. (Los Alamos, NM); Leland, Wallace T. (Los Alamos, NM); Reichelt, Walter H. (Los Alamos, NM)

1980-01-01T23:59:59.000Z

354

DNA Separation Using Photoelectrophoretic Traps  

SciTech Connect

In our recent publications we presented a design that allows formation of highly localized and optically controlled electrophoretic traps. 1,2 We demonstrated that electrophoretic traps can be utilized for biomolecule photoconcentration, optically directed transport, and separation by size. 1,2 In the current publication we suggest a hybrid design for biomolecule separation which implements electrophoretic traps in tandem with well-established electrophoretic techniques. We perform Monte Carlo simulations that demonstrate that the resolution of well-established electrophoretic techniques can be greatly enhanced by introducing photoelectrophoretic traps.

Braiman, Avital [ORNL; Thundat, Thomas George [ORNL; Rudakov, Fedor M [ORNL

2011-01-01T23:59:59.000Z

355

Anti-stratification battery separator  

Science Conference Proceedings (OSTI)

This patent describes a separator for an electric storage battery comprising a thin microporous sheet for suppressing dendrite growth between adjacent plates of the battery. The sheet has top, bottom and lateral edges defining the principal face of the separator and ribs formed on the surface of the face. The improvement described here comprises: the ribs each (1) having a concave shape, (2) being superposed one over another and (3) extending laterally across the face substantially from one the lateral edge to the other the lateral edge for reducing the accumulation of highly concentrated electrolyte at the bottom of the battery during recharge.

Stahura, D.W.; Smith, V.V. Jr.

1986-10-28T23:59:59.000Z

356

Nuclear Energy Protocol for Research Isotopes Owen Lowe  

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

Protocol for Protocol for Research Isotopes Owen Lowe Office of Isotopes for Medicine and Science Office of Nuclear Energy, Science and Technology April 16, 2002 Isotopes for Life Isotopes for Life Isotopes for Life Office of Nuclear Energy, Science and Technology Lowe/April16_02 NEPRI to NERAC.ppt (2) Nuclear Energy Protocol For Research Isotopes Nuclear Energy Protocol For Research Isotopes Why NEPRI? 6 NEPRI implements DOE funding priorities for fiscal year 2003 6 NEPRI will * Bring order to DOE's responses to requests for research isotopes * Introduce a high-quality peer review to the selection of research isotopes * Enable DOE to concentrate on operating its unique isotope production facilities Isotopes for Life Isotopes for Life Isotopes for Life Office of Nuclear Energy, Science and Technology

357

Heterodyne laser diagnostic system  

DOE Patents (OSTI)

The heterodyne laser diagnostic system includes, in one embodiment, an average power pulsed laser optical spectrum analyzer for determining the average power of the pulsed laser. In another embodiment, the system includes a pulsed laser instantaneous optical frequency measurement for determining the instantaneous optical frequency of the pulsed laser.

Globig, Michael A. (Antioch, CA); Johnson, Michael A. (Pleasanton, CA); Wyeth, Richard W. (Livermore, CA)

1990-01-01T23:59:59.000Z

358

Fusion reactions initiated by laser-accelerated particle beams in a laser-produced plasma  

E-Print Network (OSTI)

The advent of high-intensity pulsed laser technology enables the generation of extreme states of matter under conditions that are far from thermal equilibrium. This in turn could enable different approaches to generating energy from nuclear fusion. Relaxing the equilibrium requirement could widen the range of isotopes used in fusion fuels permitting cleaner and less hazardous reactions that do not produce high energy neutrons. Here we propose and implement a means to drive fusion reactions between protons and boron-11 nuclei, by colliding a laser-accelerated proton beam with a laser-generated boron plasma. We report proton-boron reaction rates that are orders of magnitude higher than those reported previously. Beyond fusion, our approach demonstrates a new means for exploring low-energy nuclear reactions such as those that occur in astrophysical plasmas and related environments.

C. Labaune; C. Baccou; S. Depierreux; C. Goyon; G. Loisel; V. Yahia; J. Rafelski

2013-10-08T23:59:59.000Z

359

Strategic Isotope Production | ornl.gov  

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

Strategic Isotope Strategic Isotope Production SHARE Strategic Isotope Production Typical capsules used in the transport of 252Cf source material inside heavily shielded shipping casks. ORNL's unique facilities at the High Flux Isotope Reactor (HFIR), Radiochemical Engineering Development Center (REDC), Irradiated Fuels Examination Laboratory (IFEL), and Irradiated Materials Examination Testing facility (IMET) are routinely used in the production, purification, packaging, and shipping of a number of isotopes of national importance, including: 75Se, 63Ni, 238Pu, 252Cf, and others. The intense neutron flux of the HFIR (2.0 x 1015 neutrons/cm²·s) permits the rapid formation of such isotopes. These highly irradiated materials are then processed and packaged for shipping using the facilities at the REDC, IFEL, and IMET.

360

Overshooting Breakthrough Curves Formed in Pressure Swing Adsorption Process for Hydrogen Isotope Separation  

Science Conference Proceedings (OSTI)

Tritium, Safety, and Environment / Eighteenth Topical Meeting on the Technology of Fusion Energy (Part 1)

K. Kotoh et al.

Note: This page contains sample records for the topic "laser isotope separation" 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

A working with a Silicon Position Sensitive Detector (dE%E calibration and isotopes separation)  

E-Print Network (OSTI)

A method for the calibration of a Silicon Position Sensitive Detector is described. From the combination of the signals collected at the ends of the resistive electrode, energy and angle of the hitting particle are reconstructed with a procedure which straightforwardly accounts for different amplifier chain gains and dc offset effects.

V. Ostashko; A. Tumino; S. Romano

2005-01-03T23:59:59.000Z

362

Automated product recovery in a HG-196 photochemical isotope separation process  

DOE Patents (OSTI)

A method of removing deposited product from a photochemical reactor used in the enrichment of .sup.196 Hg has been developed and shown to be effective for rapid re-cycling of the reactor system. Unlike previous methods relatively low temperatures are used in a gas and vapor phase process of removal. Importantly, the recovery process is understood in a quantitative manner so that scaling design to larger capacity systems can be easily carried out.

Grossman, Mark W. (Belmont, MA); Speer, Richard (Reading, MA)

1992-01-01T23:59:59.000Z

363

NATIONAL USES AND NEEDS FOR SEPARATED STABLE ISOTOPES IN PHYSICS, CHEMISTRY, AND GEOSCIENCE RESEARCH  

E-Print Network (OSTI)

State University Wichita State University KentuckyChemistry) (Physics) Kentucky University of KentuckyEastern Kentucky University University of Kentucky

Zisman, M.S.

2010-01-01T23:59:59.000Z

364

High temperature ion source for an on-line isotope separator  

DOE Patents (OSTI)

A reduced size ion source for on-line use with a cyclotron heavy-ion beam is provided. A sixfold reduction in source volume while operating with similar input power levels results in a 2000.degree. C. operating temperature. A combined target/window normally provides the reaction products for ionization while isolating the ion source plasma from the cyclotron beam line vacuum. A graphite felt catcher stops the recoiling reaction products and releases them into the plasma through diffusion and evaporation. Other target arrangements are also possible. A twenty-four hour lifetime of unattended operation is achieved, and a wider range of elements can be studied than was heretofore possible.

Mlekodaj, Ronald L. (Oak Ridge, TN)

1979-01-01T23:59:59.000Z

365

Laser-frequency multiplication  

SciTech Connect

A high quality mode locked pulse train was obtained at 9.55 micrometers, the CO2 wavelength chosen for frequency doubling into the atmospheric window at 4.8 micrometers. The pulse train consists of a 3 micro sec burst of 1.5 nsec pulses separated by 40 nsec, in a TEM(00) mode and with a total energy of 100 mJ. The pulse intensity without focussing is about 3 MW/sq.cm., already quite close to the target intensity of 10 MW/sq.cm. for frequency doubling in a AgGaSe2 crystal. The mode-locked train is obtained by intracavity modulation at 12.5 MHz using a germanium crystal driven with a power of about 30 Watts. Line selection is achieved firstly by the use of a 0.92 mm thick CaF2 plate at the Brewster angle within the cavity, which completely suppresses 10.6 micrometer band radiation. Secondly, a particular rotational line, the P20 at 9.55 micrometers, is selected by the injection of a continuous beam is mode-matched to the pulsed laser cavity using a long focal length lens, and for best line-locking it is necessary to fine tune the length of the pulsed laser resonator. Injection causes substantial depression of the gain switched spike.

Not Available

1991-11-01T23:59:59.000Z

366

Ion exchange separation and mass spectrometric analysis of uranium for solutions containing plutonium  

SciTech Connect

An ion exchange technique separates plutonium from uranium using Dowex-1 resin and a methanol--HCl plutonium elutriant. The method is applicable to both trace uranium determination and uranium isotopic distribution analysis by mass spectrometry. Distribution coefficients for plutonium, and elution curves for uranium and plutonium are shown. For uranium analysis the percent relative standard deviation is 0.8 at 120-2400 micrograms uranium per gram plutonium and 5.0 at 5 micrograms uranium per gram plutonium. (auth)

McBride, K.C.

1975-06-01T23:59:59.000Z

367

Separations innovative concepts: Project summary  

Science Conference Proceedings (OSTI)

This project summary includes the results of 10 innovations that were funded under the US Department's Innovative Concept Programs. The concepts address innovations that can substantially reduce the energy used in industrial separations. Each paper describes the proposed concept, and discusses the concept's potential energy savings, market applications, technical feasibility, prior work and state of the art, and future development needs.

Lee, V.E. (ed.)

1988-05-01T23:59:59.000Z

368

33rd Actinide Separations Conference  

SciTech Connect

Welcome to the 33rd Actinide Separations Conference hosted this year by the Lawrence Livermore National Laboratory. This annual conference is centered on the idea of networking and communication with scientists from throughout the United States, Britain, France and Japan who have expertise in nuclear material processing. This conference forum provides an excellent opportunity for bringing together experts in the fields of chemistry, nuclear and chemical engineering, and actinide processing to present and discuss experiences, research results, testing and application of actinide separation processes. The exchange of information that will take place between you, and other subject matter experts from around the nation and across the international boundaries, is a critical tool to assist in solving both national and international problems associated with the processing of nuclear materials used for both defense and energy purposes, as well as for the safe disposition of excess nuclear material. Granlibakken is a dedicated conference facility and training campus that is set up to provide the venue that supports communication between scientists and engineers attending the 33rd Actinide Separations Conference. We believe that you will find that Granlibakken and the Lake Tahoe views provide an atmosphere that is stimulating for fruitful discussions between participants from both government and private industry. We thank the Lawrence Livermore National Laboratory and the United States Department of Energy for their support of this conference. We especially thank you, the participants and subject matter experts, for your involvement in the 33rd Actinide Separations Conference.

McDonald, L M; Wilk, P A

2009-05-04T23:59:59.000Z

369

Conic separation of finite sets  

E-Print Network (OSTI)

Cancer. 95.54. 87.14. 95.86. Heart. 85.19. 80.33. 83.00. Pima. 76.30. 60.13 ... iii) An interesting subject of future research is the robustness of the separation by ...

370

Separation and purification of xenon  

DOE Patents (OSTI)

Xenon is separated from a mixture of xenon and krypton by extractive distillation using carbon tetrafluoride as the partitioning agent. Krypton is flushed out of the distillation column with CF.sub.4 in the gaseous overhead stream while purified xenon is recovered from the liquid bottoms. The distillation is conducted at about atmospheric pressure or at subatmospheric pressure.

Schlea, deceased, Carl Solomon (LATE OF Aiken, SC)

1978-03-14T23:59:59.000Z

371

Gas Separations using Ceramic Membranes  

DOE Green Energy (OSTI)

This project has been oriented toward the development of a commercially viable ceramic membrane for high temperature gas separations. A technically and commercially viable high temperature gas separation membrane and process has been developed under this project. The lab and field tests have demonstrated the operational stability, both performance and material, of the gas separation thin film, deposited upon the ceramic membrane developed. This performance reliability is built upon the ceramic membrane developed under this project as a substrate for elevated temperature operation. A comprehensive product development approach has been taken to produce an economically viable ceramic substrate, gas selective thin film and the module required to house the innovative membranes for the elevated temperature operation. Field tests have been performed to demonstrate the technical and commercial viability for (i) energy and water recovery from boiler flue gases, and (ii) hydrogen recovery from refinery waste streams using the membrane/module product developed under this project. Active commercializations effort teaming with key industrial OEMs and end users is currently underway for these applications. In addition, the gas separation membrane developed under this project has demonstrated its economical viability for the CO2 removal from subquality natural gas and landfill gas, although performance stability at the elevated temperature remains to be confirmed in the field.

Paul KT Liu

2005-01-13T23:59:59.000Z

372

METHOD AND APPARATUS FOR COLLECTING ISOTOPES  

DOE Patents (OSTI)

A method and apparatus for collecting isotopes having a high vapor pressure, such as isotopes of mercury, in a calutron are described. Heretofore, the collected material would vaporize and escape from the ion receiver as fast as it was received. By making the receiver of pure silver, the mercury isotopes form a nonvolatile amalgam with the silver at the water cooled temperature of the receiver, and the mercury is thus retained.

Leyshon, W.E.

1957-08-01T23:59:59.000Z

373

Environment/Health/Safety (EHS): Laser Safety  

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

Laser Safety Home Whom to Call Analysis of Laser Safety Occurrences: 2005-2011 Laser Bio-effects Laser Classification Laser Disposal Guide Laser Forms Laser Newsletter Laser Lab...

374

Isotopic Analysis (Not Available) | Open Energy Information  

Open Energy Info (EERE)

Usefulness not indicated DOE-funding Unknown Notes Meeting proceedings - large list of papers and presentations dealing mostly with various isotopic analyses and their applications...

375

It's Elemental - Isotopes of the Element Nobelium  

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

Mendelevium Previous Element (Mendelevium) The Periodic Table of Elements Next Element (Lawrencium) Lawrencium Isotopes of the Element Nobelium Click for Main Data Most of the...

376

It's Elemental - Isotopes of the Element Fermium  

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

Einsteinium Previous Element (Einsteinium) The Periodic Table of Elements Next Element (Mendelevium) Mendelevium Isotopes of the Element Fermium Click for Main Data Most of the...

377

WEB RESOURCE: Exploring the Table of Isotopes  

Science Conference Proceedings (OSTI)

Feb 16, 2007 ... This page offers an interactive table of isotopes, an animated glossary of nuclear terms and relevant support documents created by the ...

378

Available Technologies: Real Time High Throughput Isotopic ...  

Space exploration; Any scientific research involving the tracking of isotopic labels, as in: Solar power; Scintillators (deuterated, 10 B, 6 Li, 3 He) Batteries (doping)

379

Zeolite Cryopumps for Hydrogen Isotopes Transportation  

Science Conference Proceedings (OSTI)

Tritium Processing / Proceedings of the Fifth Topical Meeting on Tritium Technology in Fission, Fusion, and Isotopic Applications Belgirate, Italy May 28-June 3, 1995

Ivan A. Alekseev; Sergey P. Karpov; Veniamin D. Trenin

380

It's Elemental - Isotopes of the Element Rhodium  

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

Isotopes Mass Number Half-life Decay Mode Branching Percentage 89 1.5 microseconds Electron Capture (suspected) No Data Available Proton Emission (suspected) No Data Available...

Note: This page contains sample records for the topic "laser isotope separation" 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

It's Elemental - Isotopes of the Element Promethium  

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

Isotopes Mass Number Half-life Decay Mode Branching Percentage 126 No Data Available Electron Capture (suspected) No Data Available 127 No Data Available Proton Emission...

382

It's Elemental - Isotopes of the Element Niobium  

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

Isotopes Mass Number Half-life Decay Mode Branching Percentage 81 < 200 nanoseconds Electron Capture No Data Available 82 50 milliseconds Electron Capture 100.00% Electron...

383

It's Elemental - Isotopes of the Element Indium  

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

Isotopes Mass Number Half-life Decay Mode Branching Percentage 97 No Data Available Electron Capture (suspected) No Data Available Proton Emission (suspected) No Data Available...

384

It's Elemental - Isotopes of the Element Cerium  

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

Isotopes Mass Number Half-life Decay Mode Branching Percentage 119 No Data Available Electron Capture (suspected) No Data Available 120 No Data Available Electron Capture...

385

NIDC: Online Catalog of Isotope Products Home  

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

Catalog of Isotope Products Please select an option below. PRODUCTS VIEWING Select using PERIODIC TABLE or NUCLIDE CHART or LIST SEARCHING SEARCH for a Product REQUESTING REQUEST a...

386

HFIR | High Flux Isotope Reactor | ORNL  

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

HFIR Working with HFIR Neutron imaging offers new tools for exploring artifacts and ancient technology Home | User Facilities | HFIR HFIR | High Flux Isotope Reactor SHARE The High...

387

Isotopic Exchange in Air Detritiation Dryers  

Science Conference Proceedings (OSTI)

Tritium Processing / Proceedings of the Third Topical Meeting on Tritium Technology in Fission, Fusion and Isotopic Applications (Toronto, Ontario, Canada, May 1-6, 1988)

A.E. Everatt; A.H. Dombra; R.E. Johnson

388

Laser Diode Cathode Laser Diode Anode +5 Volts  

E-Print Network (OSTI)

the high performance you expect from a Wavelength component with two distinct improvements: low voltage operation from +5 V DC, and an Active Current Limit. Operating from a single +5 V supply minimizes heat dissipation. Modular packaging makes it easy to integrate the PLD into your system. For applications that require a higher forward voltage, a separate laser diode power supply input lets you provide a higher compliance voltage. The Active Current Limit not only protects your laser diode, but ensures that you are operating with maximum stability. When the laser current reaches the level set by the Limit I Trimpot, the output disables and the Limit LED and Limit Status indicate the current limit has been reached. Two photodiode ranges provide variable sensitivities for optimum operation. You can maintain excellent stability when operating in both constant current and constant power mode. All trimpots and switches are easily accessible and offer precision control. A slow start circuit, mechanical shorting relay, and Active Current Limit offer maximum protection for your laser diode even when power is removed.

H; pin Power Ground; Lim I Adj; I Disabled

2010-01-01T23:59:59.000Z

389

Design of a New Recoil Separator for Measurements of Radiative Capture Reactions in Astrophysics  

Science Conference Proceedings (OSTI)

The rates of proton- and alpha-capture reactions on unstable proton-rich nuclei are needed to understand the energy generation and element synthesis occurring in novae, X-ray bursts, and other explosions. Direct measurements of the cross sections of some of these reactions are now possible with radioactive beams and a recoil separator. A new device for such measurements, the Separator for CApture Reactions [SECAR], is being designed for use at the Facility for Rare Isotope Beams (FRIB). The specifications and preliminary conceptual design will be discussed along with plans for the first set of measurements.

Berg, Georg P. A.; Couder, Manoel; Wiescher, Michael [Dept. of Physics, Univ. of Notre Dame, Notre Dame, Indiana, 46556-5670 (United States); Joint Institute for Nuclear Astrophysics (JINA) (United States); Blackmon, Jeff C. [Dept. of Physics and Astronomy, Louisiana State Univ., Baton Rouge, Louisiana, 70803-4001 (United States); Greife, U. [Dept. of Physics, Colorado School of Mines, Golden, CO 80401 (United States); Montes, F.; Schatz, Hendrik [National Superconducting Cyclotron Laboratory, Michigan State Univ., East Lansing, Michigan, 48824 (United States); Joint Institute for Nuclear Astrophysics (JINA) (United States); Rehm, K. Ernst [Physics Division, Argonne National Lab, Argonne, Illinois, 60439 (United States); Joint Institute for Nuclear Astrophysics (JINA) (United States); Smith, Michael S. [Physics Division, Oak Ridge National Lab, Oak Ridge, Tennessee, 37831-6354 (United States); Zeller, Al [National Superconducting Cyclotron Laboratory, Michigan State Univ., East Lansing, Michigan, 48824 (United States)

2010-08-12T23:59:59.000Z

390

CLUMPED ISOTOPIC EQUILIBRIUM AND THE RATE OF ISOTOPE EXCHANGE BETWEEN CO2 AND WATER  

E-Print Network (OSTI)

CLUMPED ISOTOPIC EQUILIBRIUM AND THE RATE OF ISOTOPE EXCHANGE BETWEEN CO2 AND WATER HAGIT P. AFFEK Department of Geology and Geophysics, Yale University, 210 Whitney Ave., New Haven, Connecticut, 06511, USA the exchange of oxygen isotopes with water. The use of 18 O as an environmental indicator typically assumes

391

How do lasers work?  

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

all the way through college physics. Let me try anyway, but first let's define what a laser and laser light are. Laser is an acronym for Light Amplification by Stimulated...

392

Mercury Isotope Fractionation by Environmental Transport and Transformation Processes  

E-Print Network (OSTI)

isotope fractionation in fossil hydrothermal systems. Geology,isotopes: Evaporation, chemical diffusion and Soret diffusion. Chemical Geology,isotope records of atmospheric and riverine pollution from two major European heavy metal refineries. Chemical Geology,

Koster van Groos, Paul Gijsbert

2011-01-01T23:59:59.000Z

393

Femtosecond Laser Frequency Combs  

Science Conference Proceedings (OSTI)

... to all of these is the continued development of the lasers themselves. We are exploring and comparing different types of fs-laser comb technology ...

394

Physics Out Loud - Laser  

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

Previous Video (Hybrid Meson) Physics Out Loud Main Index Next Video (Matter) Matter Laser Learn all about different types of lasers with Jefferson Lab's Michelle Shinn, a...

395

Laser Music System.  

E-Print Network (OSTI)

?? A Laser Music System has been created, that combines a laser and light sensor system with an infrared distance sensing system that detects the… (more)

Woodruff, Astra

2012-01-01T23:59:59.000Z

396

Free Electron Laser  

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

Free Electron Laser Building Exterior Top Floor Control Room RF Gallery User Lab Beam Enclosure Injector Linear Accelerator Wiggler Magnet Return Line Free Electron Laser Most...

397

Free electron lasers  

SciTech Connect

A review of experimental and theoretical concepts of a free electron laser is given. The possibilities of scaling these lasers to high powers are discussed. (MOW)

Brau, C.A.

1980-01-01T23:59:59.000Z

398

Blind Source Separation Techniques for  

E-Print Network (OSTI)

Blind Source Separation techniques, based both on Independent Component Analysis and on second order statistics, are presented and compared for extracting partially hidden texts and textures in document images. Barely perceivable features may occur, for instance, in ancient documents previously erased and then re-written (palimpsests), or for transparency or seeping of ink from the reverse side, or from watermarks in the paper. Detecting these features can be of great importance to scholars and historians. In our approach, the document is modeled as the superposition of a number of source patterns, and a simplified linear mixture model is introduced for describing the relationship between these sources and multispectral views of the document itself. The problem of detecting the patterns that are barely perceivable in the visible color image is thus formulated as the one of separating the various patterns in the mixtures. Some examples from an extensive experimentation with real ancient documents are shown and commented.

Detecting Hidden Texts; Anna Tonazzini; Emanuele Salerno; Matteo Mochi; Luigi Bedini

2004-01-01T23:59:59.000Z

399

Molecular separation method and apparatus  

DOE Patents (OSTI)

A method and apparatus for separating a gaseous mixture of chemically identical but physically different molecules based on their polarities. The gaseous mixture of molecules is introduced in discrete quantities into the proximal end of a porous glass molecular. The molecular sieve is exposed to microwaves to excite the molecules to a higher energy state from a lower energy state, those having a higher dipole moment being excited more than those with a lower energy state. The temperature of the sieve kept cold by a flow of liquid nitrogen through a cooling jacket so that the heat generated by the molecules colliding with the material is transferred away from the material. The molecules thus alternate between a higher energy state and a lower one, with the portion of molecules having the higher dipole moment favored over the others. The former portion can then be extracted separately from the distal end of the molecular sieve.

Villa-Aleman, Eliel (3108 Roses Run, Aiken, SC 29803)

1996-01-01T23:59:59.000Z

400

Convex polytopes and quantum separability  

Science Conference Proceedings (OSTI)

We advance a perspective of the entanglement issue that appeals to the Schlienz-Mahler measure [Phys. Rev. A 52, 4396 (1995)]. Related to it, we propose a criterium based on the consideration of convex subsets of quantum states. This criterium generalizes a property of product states to convex subsets (of the set of quantum states) that is able to uncover an interesting geometrical property of the separability property.

Holik, F.; Plastino, A. [Departamento de Matematica - Ciclo Basico Comun, Universidad de Buenos Aires - Pabellon III, Ciudad Universitaria, Buenos Aires, Argentina and CONICET (Argentina); National University La Plata and CONICET IFLP-CCT, C.C. 727 - 1900 La Plata (Argentina)

2011-12-15T23:59:59.000Z

Note: This page contains sample records for the topic "laser isotope separation" 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

Method to blend separator powders  

DOE Patents (OSTI)

A method for making a blended powder mixture, whereby two or more powders are mixed in a container with a liquid selected from nitrogen or short-chain alcohols, where at least one of the powders has an angle of repose greater than approximately 50 degrees. The method is useful in preparing blended powders of Li halides and MgO for use in the preparation of thermal battery separators.

Guidotti, Ronald A. (Albuquerque, NM); Andazola, Arthur H. (Albuquerque, NM); Reinhardt, Frederick W. (Albuquerque, NM)

2007-12-04T23:59:59.000Z

402

Supported liquid membrane electrochemical separators  

DOE Patents (OSTI)

Supported liquid membrane separators improve the flexibility, efficiency and service life of electrochemical cells for a variety of applications. In the field of electrochemical storage, an alkaline secondary battery with improved service life is described in which a supported liquid membrane is interposed between the positive and negative electrodes. The supported liquid membranes of this invention can be used in energy production and storage systems, electrosynthesis systems, and in systems for the electrowinning and electrorefining of metals.

Pemsler, J. Paul (Lexington, MA); Dempsey, Michael D. (Revere, MA)

1986-01-01T23:59:59.000Z

403

Separation of Tritium from Wastewater  

Science Conference Proceedings (OSTI)

A proprietary tritium loading bed developed by Molecular Separations, Inc (MSI) has been shown to selectively load tritiated water as waters of hydration at near ambient temperatures. Tests conducted with a 126 {micro}C{sub 1} tritium/liter water standard mixture showed reductions to 25 {micro}C{sub 1}/L utilizing two, 2-meter long columns in series. Demonstration tests with Hanford Site wastewater samples indicate an approximate tritium concentration reduction from 0.3 {micro}C{sub 1}/L to 0.07 {micro}C{sub 1}/L for a series of two, 2-meter long stationary column beds Further reduction to less than 0.02 {micro}C{sub 1}/L, the current drinking water maximum contaminant level (MCL), is projected with additional bed media in series. Tritium can be removed from the loaded beds with a modest temperature increase and the beds can be reused Results of initial tests are presented and a moving bed process for treating large quantities of wastewaters is proposed. The moving bed separation process appears promising to treat existing large quantities of wastewater at various US Department of Energy (DOE) sites. The enriched tritium stream can be grouted for waste disposition. The separations system has also been shown to reduce tritium concentrations in nuclear reactor cooling water to levels that allow reuse. Energy requirements to reconstitute the loading beds and waste disposal costs for this process appear modest.

JEPPSON, D.W.

2000-01-25T23:59:59.000Z

404

Anisotropic membranes for gas separation  

DOE Patents (OSTI)

A gas separation membrane has a dense separating layer about 10,000 Angstroms or less thick and a porous support layer 10 to 400 microns thick that is an integral unit with gradually and continuously decreasing pore size from the base of the support layer to the surface of the thin separating layer and is made from a casting solution comprising ethyl cellulose and ethyl cellulose-based blends, typically greater than 47.5 ethoxyl content ethyl cellulose blended with compatible second polymers, such as nitrocellulose. The polymer content of the casting solution is from about 10% to about 35% by weight of the total solution with up to about 50% of this polymer weight a compatible second polymer to the ethyl cellulose in a volatile solvent such as isopropanol, methylacetate, methanol, ethanol, and acetone. Typical nonsolvents for the casting solutions include water and formamide. The casting solution is cast in air from about zero to 10 seconds to allow the volatile solvent to evaporate and then quenched in a coagulation bath, typically water, at a temperature of 7--25 C and then air dried at ambient temperature, typically 10--30 C. 2 figs.

Gollan, A.Z.

1987-07-21T23:59:59.000Z

405

RAPID FUSION METHOD FOR DETERMINATION OF PLUTONIUM ISOTOPES IN LARGE RICE SAMPLES  

Science Conference Proceedings (OSTI)

A new rapid fusion method for the determination of plutonium in large rice samples has been developed at the Savannah River National Laboratory (Aiken, SC, USA) that can be used to determine very low levels of plutonium isotopes in rice. The recent accident at Fukushima Nuclear Power Plant in March, 2011 reinforces the need to have rapid, reliable radiochemical analyses for radionuclides in environmental and food samples. Public concern regarding foods, particularly foods such as rice in Japan, highlights the need for analytical techniques that will allow very large sample aliquots of rice to be used for analysis so that very low levels of plutonium isotopes may be detected. The new method to determine plutonium isotopes in large rice samples utilizes a furnace ashing step, a rapid sodium hydroxide fusion method, a lanthanum fluoride matrix removal step, and a column separation process with TEVA Resin? cartridges. The method can be applied to rice sample aliquots as large as 5 kg. Plutonium isotopes can be determined using alpha spectrometry or inductively-coupled plasma mass spectrometry (ICP-MS). The method showed high chemical recoveries and effective removal of interferences. The rapid fusion technique is a rugged sample digestion method that ensures that any refractory plutonium particles are effectively digested. The MDA for a 5 kg rice sample using alpha spectrometry is 7E-5 mBq g{sup -1}. The method can easily be adapted for use by ICP-MS to allow detection of plutonium isotopic ratios.

Maxwell, S.

2013-03-01T23:59:59.000Z

406

METHOD FOR PRODUCING ISOTOPIC METHANES FROM LITHIUM CARBONATE AND LITHIUM HYDRIDE  

DOE Patents (OSTI)

A process is descrlbed for the production of methane and for the production of methane containing isotopes of hydrogen and/or carbon. Finely divided lithium hydrlde and litldum carbonate reactants are mixed in intimate contact and subsequently compacted under pressures of from 5000 to 60,000 psl. The compacted lithium hydride and lithium carbenate reactunts are dispised in a gas collecting apparatus. Subsequently, the compact is heated to a temperature in the range 350 to 400 deg C whereupon a solid-solid reaction takes place and gaseous methane is evolved. The evolved methane is contaminated with gaseous hydrogen and a very small amount of CO/sub 2/; however, the desired methane product is separated from sald impurities by well known chemical processes, e.g., condensation in a cold trap. The product methane contalns isotopes of carbon and hydrogen, the Isotopic composition being determined by the carbon isotopes originally present In the lithium carbonate and the hydrogen isotopes originally present in the lithium hydride.

Frazer, J.W.

1959-10-27T23:59:59.000Z

407

ISOTOPES  

E-Print Network (OSTI)

U.S. Department of Energy: Uranium Enrichment (1978). UnitedRaux and W.L. Grant, uranium Enrichment in South Africa,for heavy~water and uranium enrichment is more severe. In

Lederer, C. Michael

2013-01-01T23:59:59.000Z

408

ISOTOPES  

E-Print Network (OSTI)

uranium, heavy-water-moderated CANDU reactor, as contrastedis important, and in the CANDU power reactor, which uses

Lederer, C. Michael

2013-01-01T23:59:59.000Z

409

ISOTOPES  

E-Print Network (OSTI)

A Guidebook to Nuclear Reactors, University of Californiaa thermal position of a nuclear reactor followed by analysisproduced by six large nuclear reactors. The power usage per

Lederer, C. Michael

2013-01-01T23:59:59.000Z

410

ISOTOPES  

E-Print Network (OSTI)

is somewhat uncertain~ and projections have been reducedFigure 15 shows the recent CONAES projections for the U.S. (72,90), along with earlier projections for the U.S. and the

Lederer, C. Michael

2013-01-01T23:59:59.000Z

411

ISOTOPES  

E-Print Network (OSTI)

Klein and S.V. Peterson, May 9-ll, 1973, Argonne NationalLaboratory, Argonne, Illinois (1973). 97. R.A. Muller,S.V. Peterson, May 9-11, 1973, Argonne National Laboratory,

Lederer, C. Michael

2013-01-01T23:59:59.000Z

412

ISOTOPES  

E-Print Network (OSTI)

as occurs in batch distillation. The urgency of developingor one plate of a distillation column, for example. Anas in the case of a distillation column, for which any other

Lederer, C. Michael

2013-01-01T23:59:59.000Z

413

Dynamical aspects of isotopic scaling  

E-Print Network (OSTI)

Investigation of the effect of the dynamical stage of heavy-ion collisions indicates that the increasing width of the initial isospin distributions is reflected by a significant modification of the isoscaling slope for the final isotopic distributions after de-excitation. For narrow initial distributions, the isoscaling slope assumes the limiting value of the two individual initial nuclei while for wide initial isotopic distributions the slope for hot fragments approaches the initial value. The isoscaling slopes for final cold fragments increase due to secondary emissions. The experimentally observed evolution of the isoscaling parameter in multifragmentation of hot quasiprojectiles at E$_{inc}$=50 AMeV, fragmentation of $^{86}$Kr projectiles at E$_{inc}$=25 AMeV and multifragmentation of target spectators at relativistic energies was reproduced by a simulation with the dynamical stage described using the appropriate model (deep inelastic transfer and incomplete fusion at the Fermi energy domain and spectator-participant model at relativistic energies) and the de-excitation stage described with the statistical multifragmentation model. In all cases the isoscaling behavior was reproduced by a proper description of the dynamical stage and no unambiguous signals of the decrease of the symmetry energy coefficient were observed.

M. Veselsky

2006-07-17T23:59:59.000Z

414

Advanced Mass Spectrometers for Hydrogen Isotope Analyses  

DOE Green Energy (OSTI)

This report is a summary of the results of a joint Savannah River Laboratory (SRL) - Savannah River Plant (SRP) ''Hydrogen Isotope Mass Spectrometer Evaluation Program''. The program was undertaken to evaluate two prototype hydrogen isotope mass spectrometers and obtain sufficient data to permit SRP personnel to specify the mass spectrometers to replace obsolete instruments.

Chastagner, P.

2001-08-01T23:59:59.000Z

415

The Quest for the Heaviest Uranium Isotope  

E-Print Network (OSTI)

We study Uranium isotopes and surrounding elements at very large neutron number excess. Relativistic mean field and Skyrme-type approaches with different parametrizations are used in the study. Most models show clear indications for isotopes that are stable with respect to neutron emission far beyond N=184 up to the range of around N=258.

S. Schramm; D. Gridnev; D. V. Tarasov; V. N. Tarasov; W. Greiner

2011-07-06T23:59:59.000Z

416

5, 547577, 2008 Isotope hydrology of  

E-Print Network (OSTI)

HESSD 5, 547­577, 2008 Isotope hydrology of cave dripwaters L. Fuller et al. Title Page Abstract are under open-access review for the journal Hydrology and Earth System Sciences Isotope hydrology of Geology and Palaeontology, University of Innsbruck, Innrain 52, 6020 Innsbruck, Austria 3 School

Paris-Sud XI, Université de

417

Positive and inverse isotope effect on superconductivity  

E-Print Network (OSTI)

This article improves the BCS theory to include the inverse isotope effect on superconductivity. An affective model can be deduced from the model including electron-phonon interactions, and the phonon-induced attraction is simply and clearly explained on the electron Green function. The focus of this work is on how the positive or inverse isotope effect occurs in superconductors.

Tian De Cao

2009-09-04T23:59:59.000Z

418

Laser Propulsion - Quo Vadis  

SciTech Connect

First, an introductory overview of the different types of laser propulsion techniques will be given and illustrated by some historical examples. Second, laser devices available for basic experiments will be reviewed ranging from low power lasers sources to inertial confinement laser facilities. Subsequently, a status of work will show the impasse in which the laser propulsion community is currently engaged. Revisiting the basic relations leads to new avenues in ablative and direct laser propulsion for ground based and space based applications. Hereby, special attention will be devoted to the impact of emerging ultra-short pulse lasers on the coupling coefficient and specific impulse. In particular, laser sources and laser propulsion techniques will be tested in microgravity environment. A novel approach to debris removal will be discussed with respect to the Satellite Laser Ranging (SRL) facilities. Finally, some non technical issues will be raised aimed at the future prospects of laser propulsion in the international community.

Bohn, Willy L. [Institute of Technical Physics, German Aerospace Center (DLR) D-70569 Pfaffenwaldring 38-40, Stuttgart (Germany)

2008-04-28T23:59:59.000Z

419

Modern Records of Carbon and Oxygen Isotopes in Atmospheric Carbon...  

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

Modern Records of Carbon and Oxygen Isotopes in Atmospheric Carbon Dioxide and Carbon-13 in Methane Modern Records of Carbon and Oxygen Isotopes in Atmospheric Carbon Dioxide and...

420

EIS-0249: Medical Isotopes Production Project | Department of...  

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

49: Medical Isotopes Production Project EIS-0249: Medical Isotopes Production Project Summary This EIS evaluates the potential environmental impacts of a proposal to establish a...

Note: This page contains sample records for the topic "laser isotope separation" 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

Isotopic Analysis At Newberry Caldera Area (Carothers, Et Al...  

Open Energy Info (EERE)

H. Mariner, Terry E. C. Keith (1987) Isotope Geochemistry Of Minerals And Fluids From Newberry Volcano, Oregon Retrieved from "http:en.openei.orgwindex.php?titleIsotopicA...

422

Isotopic Analysis- Fluid At Indian Valley Hot Springs Geothermal...  

Open Energy Info (EERE)

Inyo and Kern Counties, California. Supplement. Isotope geochemistry and Appendix H. Final report Retrieved from "http:en.openei.orgwindex.php?titleIsotopicAnalysis-Flu...

423

CALIFORNIUM ISOTOPES FROM BOMBARDMENT OF URANIUM WITH CARBON IONS  

E-Print Network (OSTI)

Isotopes from Bombardment of Uranium with Carbon Ions A.ISOTOPES FROM BOMBARDMENT OF URANIUM WITH CARBON IONS A.the irradiations, the uranium was dissolved in dilute

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

2008-01-01T23:59:59.000Z

424

A Helium Isotope Perspective On The Dixie Valley, Nevada, Hydrothermal...  

Open Energy Info (EERE)

Helium Isotope Perspective On The Dixie Valley, Nevada, Hydrothermal System Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Journal Article: A Helium Isotope...

425

Isotopic Analysis- Rock At Long Valley Caldera Area (Smith &...  

Open Energy Info (EERE)

Isotopic Analysis- Rock At Long Valley Caldera Area (Smith & Suemnicht, 1991) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Isotopic Analysis-...

426

It's Elemental - Isotopes of the Element Radon  

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

Astatine Astatine Previous Element (Astatine) The Periodic Table of Elements Next Element (Francium) Francium Isotopes of the Element Radon [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 Radon has no naturally occurring isotopes. Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 193 1.15 milliseconds Alpha Decay 100.00% 194 0.78 milliseconds Alpha Decay 100.00% 195 6 milliseconds Alpha Decay 100.00% 195m 5 milliseconds Alpha Decay 100.00% 196 4.4 milliseconds Alpha Decay 99.90% Electron Capture ~ 0.10% 197 53 milliseconds Alpha Decay 100.00% 197m 25 milliseconds Alpha Decay 100.00% 198 65 milliseconds Alpha Decay No Data Available

427

It's Elemental - Isotopes of the Element Francium  

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

Radon Radon Previous Element (Radon) The Periodic Table of Elements Next Element (Radium) Radium Isotopes of the Element Francium [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 Francium has no naturally occurring isotopes. Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 199 12 milliseconds Alpha Decay > 0.00% Electron Capture No Data Available 200 49 milliseconds Alpha Decay 100.00% 201 62 milliseconds Alpha Decay 100.00% 201m 19 milliseconds Alpha Decay 100.00% 202 0.30 seconds Alpha Decay 100.00% 202m 0.29 seconds Alpha Decay 100.00% 203 0.55 seconds Alpha Decay <= 100.00% 204 1.8 seconds Alpha Decay 92.00%

428

Selected Isotopes for Optimized Fuel Assembly Tags  

SciTech Connect

In support of our ongoing signatures project we present information on 3 isotopes selected for possible application in optimized tags that could be applied to fuel assemblies to provide an objective measure of burnup. 1. Important factors for an optimized tag are compatibility with the reactor environment (corrosion resistance), low radioactive activation, at least 2 stable isotopes, moderate neutron absorption cross-section, which gives significant changes in isotope ratios over typical fuel assembly irradiation levels, and ease of measurement in the SIMS machine 2. From the candidate isotopes presented in the 3rd FY 08 Quarterly Report, the most promising appear to be Titanium, Hafnium, and Platinum. The other candidate isotopes (Iron, Tungsten, exhibited inadequate corrosion resistance and/or had neutron capture cross-sections either too high or too low for the burnup range of interest.

Gerlach, David C.; Mitchell, Mark R.; Reid, Bruce D.; Gesh, Christopher J.; Hurley, David E.

2008-10-01T23:59:59.000Z

429

Integrated Laser-Target Interaction Experiments on the RAL Petawatt Laser  

Science Conference Proceedings (OSTI)

Since the construction of the first Petawatt laser on the Nova laser facility at Lawrence Livermore National Laboratory we are witnessing the emergence of similar Petawatt-class laser systems at laboratories all around the world. This new generation of lasers, able to deliver several hundred joules of energy in a sub-picosecond pulse, has enabled a host of new discoveries to be made and continues to provide a valuable tool to explore new regimes in relativistic laser-plasma physics--encompassing high energy X-rays and -rays, relativistic electrons, intense ion beams, and superstrong magnetic fields. The coupling in the near-future of multi-kiloJoule Petawatt-class lasers with large-scale fusion lasers.including the NIF and Omega EP (US), LIL (France), and FIREX (Japan)--will further expand opportunities in fast ignition, high energy X-ray radiography, and high energy density physics research. The 500 J Petawatt laser at the Rutherford Appleton Laboratory is currently the highest energy short-pulse laser in the world. In this paper we describe a recent experimental campaign carried out on the facility. The campaign, performed by a large collaborative team from eight different laboratories, was designed to study a variety of relativistic laser-interaction phenomena including laser absorption, fast electron transport, proton heating, and high-brightness x-ray generation. The wide scope of the experiment necessitated the deployment of a very large set of diagnostics--in total twenty-five separate instruments. In order to obtain the most comprehensive set of measurements all twenty-five diagnostics were fielded simultaneously on every shot.

Patel, P K; Key, M H; Mackinnon, A J; Berry, R; Borghesi, M; Chambers, D M; Chen, H; Clarke, R; Damian, C; Eagleton, R; Freeman, R; Glenzer, S; Gregori, G; Heathcote, R; Hey, D; Izumi, N; Kar, S; King, J; Nikroo, A; Niles, A; Park, H S; Pasley, J; Patel, N; Shepherd, R; Snavely, R A; Steinman, D; Stoeckl, C; Storm, M; Town, R; Van Maren, R; Theobald, W; Wilks, S C; Zhang, B

2006-10-11T23:59:59.000Z

430

Apparatus and method for separating constituents  

DOE Patents (OSTI)

A centrifugal separator apparatus and method for improving the efficiency of the separation of constituents in a fluid stream. A cyclone separator includes an assembly for separately discharging both constituents through the same end of the separator housing. A rotary separator includes a rotary housing having a baffle disposed therein for minimizing the differential rotational velocities of the constituents in the housing, thereby decreasing turbulence, and increasing efficiency. The intensity of the centrifugal force and the time which the constituents reside within the housing can be independently controlled to improve efficiency of separation.

Maronde, Carl P. (McMurray, PA); Killmeyer, Jr., Richard P. (Pittsburgh, PA)

1992-01-01T23:59:59.000Z

431

SEPARATION OF PROTACTINIUM FROM CONTAMINANTS  

DOE Patents (OSTI)

The separation of protactinium by volatilization method is described. According to the invention, neutron irradiated finely divided thorium is reacted with aluminum trichloride or a mixture of aluminum trichloride and chlorine gas at a temperature of preferably between about 200 and 400 deg C. Following the chlorinating step the protactinium chloride along with aluminum chloride is selectively distilled from the mixture at a temperature of approximately 100 deg C. The protactinium chloride may be recovered from the mixture by treatment with sodium hydroxide, which converts the aluminum chloride to a soluble salt and forms insoluble protactinium hydroxide.

Malm, J.G.; Fried, S.

1959-07-01T23:59:59.000Z

432

Separation of actinides from lanthanides  

DOE Patents (OSTI)

An organic extracting solution and an extraction method useful for separating elements of the actinide series of the periodic table from elements of the lanthanide series, where both are in trivalent form is described. The extracting solution consists of a primary ligand and a secondary ligand, preferably in an organic solvent. The primary ligand is a substituted monothio-1,3-dicarbonyl, which includes a substituted 4-acyl-2-pyrazolin-5-thione, such as 4-benzoyl-2,4- dihydro-5-methyl-2-phenyl-3H-pyrazol-3-thione (BMPPT). The secondary ligand is a substituted phosphine oxide, such as trioctylphosphine oxide (TOPO).

Smith, B.F.; Jarvinen, G.D.; Ryan, R.R.

1988-03-31T23:59:59.000Z

433

SEPARATION OF URANIUM FROM THORIUM  

DOE Patents (OSTI)

A process is presented for separating uranium from thorium wherein the ratio of thorium to uranium is between 100 to 10,000. According to the invention the thoriumuranium mixture is dissolved in nitric acid, and the solution is prepared so as to obtain the desired concentration within a critical range of from 4 to 8 N with regard to the total nitrate due to thorium nitrate, with or without nitric acid or any nitrate salting out agent. The solution is then contacted with an ether, such as diethyl ether, whereby uranium is extracted into ihe organic phase while thorium remains in the aqueous phase.

Hellman, N.N.

1959-07-01T23:59:59.000Z

434

SEPARATION OF THORIUM FROM URANIUM  

DOE Patents (OSTI)

A description is given for the separation of thorium from uranium by forming an aqueous acidic solution containing ionic species of thorium, uranyl uranium, and hydroxylamine, flowing the solution through a column containing the phenol-formaldehyde type cation exchange resin to selectively adsorb substantially all the thorium values and a portion of the uranium values, flowing a dilute solution of hydrochloric acid through the column to desorb the uranium values, and then flowing a dilute aqueous acidic solution containing an ion, such as bisulfate, which has a complexing effect upon thortum through the column to desorb substantially all of the thorium.

Bane, R.W.

1959-09-01T23:59:59.000Z

435

Narrow gap laser welding  

SciTech Connect

A laser welding process including: (a) using optical ray tracing to make a model of a laser beam and the geometry of a joint to be welded; (b) adjusting variables in the model to choose variables for use in making a laser weld; and (c) laser welding the joint to be welded using the chosen variables.

Milewski, John O. (Santa Fe, NM); Sklar, Edward (Santa Fe, NM)

1998-01-01T23:59:59.000Z

436

Narrow gap laser welding  

DOE Patents (OSTI)

A laser welding process including: (a) using optical ray tracing to make a model of a laser beam and the geometry of a joint to be welded; (b) adjusting variables in the model to choose variables for use in making a laser weld; and (c) laser welding the joint to be welded using the chosen variables. 34 figs.

Milewski, J.O.; Sklar, E.

1998-06-02T23:59:59.000Z

437

Longitudinal discharge laser baffles  

DOE Patents (OSTI)

The IR baffles placed between the window and the electrode of a longitudinal discharge laser improve laser performance by intercepting off-axis IR radiation from the laser and in doing so reduce window heating and subsequent optical distortion of the laser beam.

Warner, Bruce E. (Livermore, CA); Ault, Earl R. (Dublin, CA)

1994-01-01T23:59:59.000Z

438

Longitudinal discharge laser baffles  

DOE Patents (OSTI)

The IR baffles placed between the window and the electrode of a longitudinal discharge laser improve laser performance by intercepting off-axis IR radiation from the laser and in doing so reduce window heating and subsequent optical distortion of the laser beam. 1 fig.

Warner, B.E.; Ault, E.R.

1994-06-07T23:59:59.000Z

439

Laser Glazing of Railroad Rails [Laser Applications Laboratory] - Nuclear  

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

Laser Glazing of Railroad Laser Glazing of Railroad Rails Capabilities Engineering Experimentation Reactor Safety Experimentation Aerosol Experiments System Components Laser Applications Overview Laser Oil & Gas Well Drilling Laser Heat Treatment Laser Welding of Metals On-line Monitoring Laser Beam Delivery Laser Glazing of Railroad Rails High Power Laser Beam Delivery Decontamination and Decommissioning Refractory Alloy Welding Robots Applications Other Facilities Other Capabilities Work with Argonne Contact us For Employees Site Map Help Join us on Facebook Follow us on Twitter NE on Flickr Laser Applications Laboratory Laser Glazing of Railroad Rails Project description: Laser glazing of rails. Category: Project with industrial partner (American Association of Railroads) Bookmark and Share

440

Laser Welding of Metals [Laser Applications Laboratory] - Nuclear  

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

Laser Welding of Metals Laser Welding of Metals Capabilities Engineering Experimentation Reactor Safety Experimentation Aerosol Experiments System Components Laser Applications Overview Laser Oil & Gas Well Drilling Laser Heat Treatment Laser Welding of Metals On-line Monitoring Laser Beam Delivery Laser Glazing of Railroad Rails High Power Laser Beam Delivery Decontamination and Decommissioning Refractory Alloy Welding Robots Applications Other Facilities Other Capabilities Work with Argonne Contact us For Employees Site Map Help Join us on Facebook Follow us on Twitter NE on Flickr Laser Applications Laboratory Laser Welding of Metals Project description: High-speed laser welding of metals. Category: Project with industrial partner (Delphi Energy and Engine Management Systems) Bookmark and Share

Note: This page contains sample records for the topic "laser isotope separation" 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

Laser Guiding for GeV Laser-Plasma Accelerators  

E-Print Network (OSTI)

Light pipe for high intensity laser pulses. Phys. Rev. Lett.and relativistically strong laser pulses in an underdensefrom Thomson scat- tering using laser wake?eld accelerators.

Leemans, Wim; Esarey, Eric; Geddes, Cameron; Schroeder, C.B.; Toth, Csaba

2005-01-01T23:59:59.000Z

442

Nonlinear laser energy depletion in laser-plasma accelerators  

E-Print Network (OSTI)

Nonlinear laser energydepletion in laser-plasma accelerators ? B. A. Shadwick,of intense, short-pulse lasers via excitation of plasma

Shadwick, B.A.

2009-01-01T23:59:59.000Z

443

Ultracentrifuge for separating fluid mixtures  

DOE Patents (OSTI)

1. A centrifuge for the separation of fluid mixtures having light and heavy fractions comprising a cylindrical rotor, disc type end-plugs closing the ends of the rotor, means for mounting said rotor for rotation about its cylindrical axis, a housing member enclosing the rotor, a vacuum chamber in said housing about the central portion of the rotor, a collection chamber at each end of the housing, the innermost side of which is substantially formed by the outer face of the end-plug, means for preventing flow of the fluid from the collection chambers to said vacuum chamber, at least one of said end-plugs having a plurality of holes therethrough communicating between the collection chamber adjacent thereto and the inside of the rotor to induce countercurrent flow of the fluid in the centrifuge, means for feeding fluid to be processed into the centrifuge, means communicating with the collection chambers to extract the light and heavy separated fractions of the fluid, and means for rotating the rotor.

Lowry, Ralph A. (Charlottesville, VA)

1976-01-01T23:59:59.000Z

444

Separations and safeguards model integration.  

Science Conference Proceedings (OSTI)

Research and development of advanced reprocessing plant designs can greatly benefit from the development of a reprocessing plant model capable of transient solvent extraction chemistry. This type of model can be used to optimize the operations of a plant as well as the designs for safeguards, security, and safety. Previous work has integrated a transient solvent extraction simulation module, based on the Solvent Extraction Process Having Interaction Solutes (SEPHIS) code developed at Oak Ridge National Laboratory, with the Separations and Safeguards Performance Model (SSPM) developed at Sandia National Laboratory, as a first step toward creating a more versatile design and evaluation tool. The goal of this work was to strengthen the integration by linking more variables between the two codes. The results from this integrated model show expected operational performance through plant transients. Additionally, ORIGEN source term files were integrated into the SSPM to provide concentrations, radioactivity, neutron emission rate, and thermal power data for various spent fuels. This data was used to generate measurement blocks that can determine the radioactivity, neutron emission rate, or thermal power of any stream or vessel in the plant model. This work examined how the code could be expanded to integrate other separation steps and benchmark the results to other data. Recommendations for future work will be presented.

Cipiti, Benjamin B.; Zinaman, Owen

2010-09-01T23:59:59.000Z

445

Innovative oxygen separation membrane prototype  

SciTech Connect

Improvements are still needed to gas separation processes to gain industry acceptance of coal gasification systems. The Ion Transport Membrane (ITM) technology, being developed by the US Department of Energy and its partners, offers an opportunity to lower overall plant cost and improve efficiency compared to cryogenic distillation and pressure swing adsorption methods. The technology is based on a novel class of perovskite ceramic oxides which can selectively separate oxygen ions from a stream of air at high temperature and pressure. Those ions are transported across the ITM leaving non-permeate air which can be integrated with a fuel-fired gas system, enabling co-production of power and steam along with the concentrated, high-purity oxygen. The project is at the second phase, to scale up the ITM Oxygen ceramic devices to demonstrate the technology at the 1-5 tpd capability in the Subscale Engineering Prototype. A third phase to demonstrate commercial viability extends to the end of the decade. 2 figs.

NONE

2006-08-15T23:59:59.000Z

446

Apparatus for storing hydrogen isotopes  

DOE Green Energy (OSTI)

An improved method and apparatus for storing isotopes of hydrogen (especially tritium) are provided. The hydrogen gas(es) is (are) stored as hydrides of material (for example uranium) within boreholes in a block of copper. The mass of the block is critically important to the operation, as is the selection of copper, because no cooling pipes are used. Because no cooling pipes are used, there can be no failure due to cooling pipes. And because copper is used instead of stainless steel, a significantly higher temperature can be reached before the eutectic formation of uranium with copper occurs, (the eutectic of uranium with the iron in stainless steel forming at a significantly lower temperature).

McMullen, John W. (Los Alamos, NM); Wheeler, Michael G. (Los Alamos, NM); Cullingford, Hatice S. (Houston, TX); Sherman, Robert H. (Los Alamos, NM)

1985-01-01T23:59:59.000Z

447

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

Science Conference Proceedings (OSTI)

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

Grate, Jay W.; O'Hara, Matthew J.; Farawila, Anne F.; Douglas, Matthew; Haney, Morgan M.; Peterson, Steve L.; Maiti, Tapas C.; Aardahl, Christopher L.

2011-10-17T23:59:59.000Z

448

Vibrational, rotational, and isotopic dependence of CaBr X/sup 2/. sigma. spin-rotational and HFS parameters  

Science Conference Proceedings (OSTI)

The previously published molecular-beam, laser-rf, double-resonance study of the rotational and isotopic dependences of the spin-rotational and hyperfine interactions in the v'' = 0, X/sup 2/..sigma.. state of CaBr is supplemented here with data for v''=1. The vibrational dependence of the parameters is now obtained. The results for CaBr are displayed along with analogous, previously published results for CaF and CaCl.

Childs, W.J.; Cok, D.R.; Goodman, L.S.

1982-01-01T23:59:59.000Z

449

Selenide isotope generator for the Galileo Mission. Program final report  

SciTech Connect

This final report for the Selenide Isotope Generator for the Galileo Mission (SIG/GM) documents the work performed by Teledyne Energy Systems (TES) under US Department of Energy (DOE) Contract No. DE-AC01-78ET33009 (formerly ET-78-C-01-2865) during the period April 10, 1978 to June 30, 1979. Because of technical difficulties with the thermoelectric converter being developed by the 3M Company under separate DOE contract, a Stop Work Order, dated January 29, 1979, was issued by DOE. The TES effort up to the receipt of the Stop Work Order as well as limited technical activities up to the contract conclusion on June 30, 1979 are reported.

1979-06-01T23:59:59.000Z

450

Seven Channel Multi-collector Isotope Ratio Mass Spectrometer  

Science Conference Proceedings (OSTI)

A new magnetic sector mass spectrometer that utilizes seven full-sized discrete dynode electron multipliers operating simultaneously has been designed, constructed and is in preliminary testing. The instrument utilizes a newly developed ion dispersion lens that enables the mass dispersed individual isotope beams to be separated sufficiently (35 mm) to allow a full-sized discrete dynode pulse counting multiplier to be used for each beam. The ion dispersion lens is a two element electrostatic 90 degree sector device that causes the beam-to-beam dispersion to increase faster than the intra-beam dispersion. Each multiplier is contained in an isolated case with a deflector/condenser lens at the entrance. A 9-sample filament cartridge is mounted on a micro-manipulator two-axis stage that enables adjustment of the filament position with 10 micron resolution within the ion lens. Results of initial testing with actinides will be presented.

Anthony D. Appelhans

2008-07-01T23:59:59.000Z

451

LANL | Physics | Trident Laser Facility  

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

science at Trident Laser Facility Several important discoveries and first observations have been made at the Trident Laser Facility, a unique three-beam neodymium-glass laser...

452

Engineering the Petawatt Laser into Nova  

SciTech Connect

The engineering process of integrating the Petawatt (10{sup 15} watts) laser system into the existing 30 kJ (UV) Nova laser at Lawrence Livermore National Laboratory (LLNL) is described in detail. The nanosecond-long, chirped Petawatt laser pulse is initially generated in a separate master oscillator room and then injected into one of Nova`s 10 beamlines. There, the pulse is further amplified and enlarged to {approximately}{phi}60 cm, temporally compressed under vacuum to <500 fs using large diameter diffraction gratings, and then finally focused onto targets using a parabolic mirror. The major Petawatt components are physically large which created many significant engineering challenges in design, installation and implementation. These include the diffraction gratings and mirrors, vacuum compressor chamber, target chamber, and parabolic focusing mirror. Other Petawatt system components were also technically challenging and include: an injection beamline, transport spatial filters, laser diagnostics, alignment components, motor controls, interlocks, timing and synchronization systems, support structures, and vacuum systems. The entire Petawatt laser system was designed, fabricated, installed, and activated while the Nova laser continued its normal two-shift operation. This process required careful engineering and detailed planning to prevent experimental downtime and to complete the project on schedule.

Tietbohl, G.L.; Bell, P.M.; Hamilton, R.M. [and others

1997-12-23T23:59:59.000Z

453

Astrophysical image separation by blind time--frequency source separation methods  

Science Conference Proceedings (OSTI)

In this paper, two prevalent blind time-frequency (TF) source separation methods in the literature are adapted to astrophysical image mixtures and four algorithms are developed to separate them into their astrophysical components. The components considered ... Keywords: Astrophysical image separation, Blind time--frequency source separation methods, Cosmic microwave background radiation, Joint diagonalization, Source separation

Mehmet Tankut Özgen; Ercan Engin Kuruo?lu; Diego Herranz

2009-03-01T23:59:59.000Z

454

Process for strontium-82 separation  

DOE Patents (OSTI)

The process is for the selective separation of Sr-82 and Sr-85 from a proton-irradiated Mo target. It includes dissolving the Mo in H2O2 to form a solution which is then passed through a cationic resin, whereby Mo, Nb, Tc, Se, V, As, Ge, Zr, Rb ions remain in the solution, while Rb, Zn, Be, Co, Fe, Mn, Cr, Sr, Y, Zr ions are adsorbed. The resin is contacted with an acid solution to remove the adsorbed ions, forming a second solution. The second solution is evaporated and the residue dissolved in a dilute acid to form a third solution. After adjusting the acid molarity, the third solution is passed through a second cationic resin; this resin is contacted first with a dilute sulfuric acid solution and then with a dilute acid solution to remove the adsorbed Sr ions. Zr, Rb, and Y radioisotopes can also be recovered with additional steps.

Heaton, R.C.; Jamriska, D.J. Sr.; Taylor, W.A.

1991-12-31T23:59:59.000Z

455

Olefin separation membrane and process  

DOE Patents (OSTI)

A membrane and process are disclosed for separating unsaturated hydrocarbons from fluid mixtures. The membrane and process differ from previously known membranes and processes, in that the feed and permeate streams can both be dry, the membrane need not be water or solvent swollen, and the membrane is characterized by a selectivity for an unsaturated hydrocarbon over a saturated hydrocarbon having the same number of carbon atoms of at least about 20, and a pressure-normalized flux of said unsaturated hydrocarbon of at least about 5{times}10{sup {minus}6}cm{sup 3}(STP)/cm{sup 2}{center_dot}s{center_dot}cmHg, said flux and selectivity being measured with a gas mixture containing said unsaturated and saturated hydrocarbons, and in a substantially dry environment. 4 figs.

Pinnau, I.; Toy, L.G.; Casillas, C.

1997-09-23T23:59:59.000Z

456

SEPARATION PROCESS FOR THORIUM SALTS  

DOE Patents (OSTI)

A process is described for the separation of uranium, thorium, and rare earths extracted from monazite by digesting with sulfuric acid. By carefully increasing the pH of the solution, stepwise, over the range 0.8 to 5.5, a series of selective precipitations will be achieved, with the thorium values coming out at lower pH, the rare earths at intermediate pH and the uranium last. Some mixed precipitates will be obtained, and these may be treated by dissolving in HNO/sub 3/ and contacting with dibutyl phosphate, whereby thorium or uranium are taken up by the organic phase while the rare earths preferentially remain in the aqueous solution.

Bridger, G.L.; Whatley, M.E.; Shaw, K.G.

1957-12-01T23:59:59.000Z

457

Separation of magnetic field lines  

SciTech Connect

The field lines of magnetic fields that depend on three spatial coordinates are shown to have a fundamentally different behavior from those that depend on two coordinates. Unlike two-coordinate cases, a flux tube in a magnetic field that depends on all three spatial coordinates that has a circular cross section at one location along the tube characteristically has a highly distorted cross section at other locations. In an ideal evolution of a magnetic field, the current densities typically increase. Crudely stated, if the current densities increase by a factor {sigma}, the ratio of the long to the short distance across a cross section of a flux tube characteristically increases by e{sup 2{sigma}}, and the ratio of the longer distance to the initial radius increases as e{sup {sigma}}. Electron inertia prevents a plasma from isolating two magnetic field structures on a distance scale shorter than c/{omega}{sub pe}, which is about 10 cm in the solar corona, and reconnection must be triggered if {sigma} becomes sufficiently large. The radius of the sun, R{sub Circled-Dot-Operator }=7 Multiplication-Sign 10{sup 10}cm is about e{sup 23} times larger, so when {sigma} Greater-Than-Or-Equivalent-To 23, two lines separated by c/{omega}{sub pe} at one location can be separated by the full scale of any magnetic structures in the corona at another. The conditions for achieving a large exponentiation, {sigma}, are derived, and the importance of exponentiation is discussed.

Boozer, Allen H. [Department of Applied Physics and Applied Mathematics, Columbia University, New York, New York 10027 (United States)

2012-11-15T23:59:59.000Z

458

Gas separation with glass membranes  

DOE Green Energy (OSTI)

The Department of Energy (DOE) is seeking to develop high temperature, high pressure inorganic membrane technology to perform a variety of gas separation processes to improve the efficiency and economics of advanced power generation systems such as direct coal-fueled turbines (DCFT) and the integrated gasification combined cycle process (IGCC). The temperatures encountered in these power generation systems are far above the temperature range for organic membrane materials. Inorganic materials such as ceramics are therefore the most likely membrane materials for use at high temperatures. This project focussed on silica glass fiber membranes made by PPG Industries (Pittsburgh, PA). The goals were both experimental and theoretical. The first objective was to develop a rational theory for the performance of these membranes. With existing theories as a starting point, a new theory was devised to explain the unusual molecular sieving'' behavior exhibited by these glass membranes. An apparatus was then devised for making permeation performance measurements at conditions of interest to DOE (temperatures to 2000[degrees]F; pressures to 1000 psia). With this apparatus, gas mixtures could be made typical of coal combustion or coal gasification processes, these gases could be passed into a membrane test cell, and the separation performance determined. Data were obtained for H[sub 2]/CO,N[sub 2]/CO[sub 2], 0[sub 2]/N[sub 2], and NH[sub 3]/N[sub 2] mixtures and for a variety of pure component gases (He, H[sub 2], CO[sub 2], N[sub 2], CO, NH[sub 3]). The most challenging part of the project turned out to be the sealing of the membrane at high temperatures and pressures. The report concludes with an overview of the practical potential of these membranes and of inorganic membranes in general of DOE and other applications.

Roberts, D.L.; Abraham, L.C.; Blum, Y.; Way, J.D.

1992-05-01T23:59:59.000Z

459

Rapid separation of individual rare-earth elements from fission products  

SciTech Connect

A microprocessor-controlled radiochemical separation system has been developed to rapidly separate rare-earth elements from gross fission products. The system is composed of two high performance liquid chromatography columns coupled in series by a stream-splitting injection valve. The first column separates the rare-earth group by extraction chromatography using dihexyldiethylcarbamylmethylenephosphonate (DHDECMP) adsorbed on Vydac C/sub 8/ resin. The second column isolates the individual rare-earth elements by cation exchange using Aminex A-9 resin with ..cap alpha..-hydroxyisobutyric acid (..cap alpha..-HIBA) as the eluent. With this system, fission-product rare-earth isotopes with half-lives as short as three minutes have been studied.

Baker, J.D.; Gehrke, R.J.; Greenwood, R.C.; Meikrantz, D.H.

1980-01-01T23:59:59.000Z

460

Formation of periodic structures upon laser ablation of metal targets in liquids  

SciTech Connect

Experimental data on the formation of ordered microstructures produced upon ablation of metal targets in liquids irradiated by a copper vapour laser or a pulsed Nd:YAG laser are presented. The structures were obtained on brass, bronze, copper, and tungsten substrates immersed in distilled water or ethanol. As a result of multiple-pulse laser ablation by a scanning beam, ordered microcones with pointed vertexes are formed on the target surface. The structures are separated by deep narrow channels. The structure period was experimentally shown to increase linearly with diameter of the laser spot on the target surface. (interaction of laser radiation with matter)

Kazakevich, Pavel V; Simakin, Aleksandr V; Shafeev, Georgii A [A.M. Prokhorov General Physics Institute, Russian Academy of Sciences, Moscow (Russian Federation)

2005-09-30T23:59:59.000Z

Note: This page contains sample records for the topic "laser isotope separation" 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

Feasibility Study on Laser Microwelding and Laser Shock Peening using Femtosecond Laser Pulses.  

E-Print Network (OSTI)

??Ultrafast lasers of sub-picosecond pulse duration have thus far been investigated for ablation, drilling and cutting processes. Ultrafast lasers also have the potential for laser… (more)

Lee, Dongkyun

2008-01-01T23:59:59.000Z

462

BNL | CO2 Laser  

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

CO2 Laser CO2 Laser The ATF is one of the only two facilities worldwide operating picosecond, terawatt-class CO2 lasers. Our laser system consists of a picoseconds pulse-injector based on fast optical switching from the output of a conventional CO2 laser oscillator, and a chain of high-pressure laser amplifiers. It starts with a wavelength converter wherein a near-IR picosecond solid-state laser with l»1 μm produces a mid-IR 10-μm pulse. This process employs two methods; semiconductor optical switching, and the Kerr effect. First, we combine the outputs from a multi-nanosecond CO2 laser oscillator with a picosecond Nd:YAG laser on a germanium Brewster-plate to produce an ~200 ps, 10μm pulse by semiconductor optical switching. Co-propagating this pulse with a Nd:YAG's 2nd harmonic in a

463

Norman Ramsey and the Separated Oscillatory Fields Method  

Office of Scientific and Technical Information (OSTI)

Norman Ramsey and the Norman Ramsey and the Separated Oscillatory Fields Method Resources with Additional Information Norman F. Ramsey Photo Credit: Courtesy of Fermilab Norman F. Ramsey was born in Washington, D.C. and 'was educated in the United States and England; he earned five degrees in physics including the Ph.D. (Columbia 1940) and the D.Sc. (Cambridge, 1964). Ramsey's scientific research focused on the properties of molecules, atoms, nuclei and elementary particles and includes key contributions to the knowledge of magnetic moments, the structural shape of nuclear particles, the nature of nuclear forces, the thermodynamics of energized populations of atoms and molecules (e.g. those in masers and lasers) and spectroscopy. Ramsey not only contributed basic advances in the theoretical understanding of the physics involved in his research, he also made pioneering advances in the methods of investigation; in particular, he contributed many refinements of the molecular beam method for the study of atomic and molecular properties, he invented the separated oscillatory field method of exciting resonances and, with the collaboration of his students, he was the principal inventor of the atomic hydrogen maser. The separated oscillatory field method provides extremely high resolution in atomic and molecular spectroscopy and it is the practical basis for the most precise atomic clocks; likewise the atomic hydrogen maser made even higher levels of spectroscopic resolution possible and it also functions as the basis for atomic clocks having the highest levels of stability for periods extending to several hours.'1

464

OPTIMUM ENERGY ABSORPTION OF A SHORT-PULSE LASER IN A DOPED DIELECTRIC SLAB  

SciTech Connect

A model is used to calculate energy absorption efficiency when a short-pulse laser impinges on a dielectric slab doped with an impurity for which the electrons have a resonant line at the laser wavelength. The amount of the energy resonant absorption is due to the overlapping between laser spectrum and resonance spectrum. The energy absorption efficiency can be maximized for a certain degree of doping concentration (at a given pulselength) and also for a certain pulselength (at a given doping concentration). For a modest amount of impurity, the resonant absorption may increase the fraction of energy absorption up to tens of percent of laser energy at 100s optical cycles when the laser wavelength is tuned within 1% of the resonant line. Dimensionless parameters are constructed so that the scaling to various parameters: laser wavelength, laser pulselength, dielectric constant, slab thickness, impurity concentration, resonant linewidth, and separation between the laser wavelength and the line resonance, could easily be obtained.

L. ANG

2001-05-01T23:59:59.000Z

465

Method for selecting hollow microspheres for use in laser fusion targets  

DOE Patents (OSTI)

Hollow microspheres having thin and very uniform wall thickness are useful as containers for the deuterium and tritium gas mixture used as a fuel in laser fusion targets. Hollow microspheres are commercially available; however, in commercial lots only a very small number meet the rigid requirements for use in laser fusion targets. Those meeting these requirements may be separated from the unsuitable ones by subjecting the commercial lot to size and density separations and then by subjecting those hollow microspheres thus separated to an external pressurization at which those which are aspherical or which have nonuniform walls are broken and separating the sound hollow microspheres from the broken ones.

Farnum, Eugene H. (Los Alamos, NM); Fries, R. Jay (Los Alamos, NM); Havenhill, Jerry W. (Independence, MO); Smith, Maurice Lee (Kansas City, MO); Stoltz, Daniel L. (Blue Springs, MO)

1976-01-01T23:59:59.000Z

466

Preface to bLithium isotope geochemistryQ The use of light stable isotopes to elucidate Earth  

E-Print Network (OSTI)

Li reflect heavier isotopic ratios. Chemical Geology 212 (2004) 1­4 wwwPreface Preface to bLithium isotope geochemistryQ The use of light stable isotopes to elucidate isotope geochemistry. Taylor and Urey (1938) used ion exchange chromatography to sepa- rate 6 Li from 7 Li

Rudnick, Roberta L.

467

Image Source Separation Using Color Channel Dependencies  

Science Conference Proceedings (OSTI)

We investigate the problem of source separation in images in the Bayesian framework using the color channel dependencies. As a case in point we consider the source separation of color images which have dependence between its components. A Markov Random ...

Koray Kayabol; Ercan E. Kuruoglu; Bulent Sankur

2009-03-01T23:59:59.000Z

468

It's Elemental - Isotopes of the Element Boron  

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

Beryllium Beryllium Previous Element (Beryllium) The Periodic Table of Elements Next Element (Carbon) Carbon Isotopes of the Element Boron [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 10 19.9% STABLE 11 80.1% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 6 No Data Available Double Proton Emission (suspected) No Data Available 7 3.255Ă—10-22 seconds Proton Emission No Data Available Alpha Decay No Data Available 8 770 milliseconds Electron Capture 100.00% Electron Capture with delayed Alpha Decay 100.00% 9 8.439Ă—10-19 seconds Proton Emission 100.00% Double Alpha Decay 100.00%

469

It's Elemental - Isotopes of the Element Tungsten  

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

Tantalum Tantalum Previous Element (Tantalum) The Periodic Table of Elements Next Element (Rhenium) Rhenium Isotopes of the Element Tungsten [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 180 0.12% >= 6.6Ă—10+17 years 182 26.50% STABLE 183 14.31% > 1.3Ă—10+19 years 184 30.64% STABLE 186 28.43% > 2.3Ă—10+19 years Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 157 275 milliseconds Electron Capture No Data Available 158 1.25 milliseconds Alpha Decay 100.00% 158m 0.143 milliseconds Isomeric Transition No Data Available Alpha Decay No Data Available 159 7.3 milliseconds Alpha Decay ~ 99.90%

470

It's Elemental - Isotopes of the Element Carbon  

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

Boron Boron Previous Element (Boron) The Periodic Table of Elements Next Element (Nitrogen) Nitrogen Isotopes of the Element Carbon [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 12 98.93% STABLE 13 1.07% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 8 1.981Ă—10-21 seconds Proton Emission 100.00% Alpha Decay No Data Available 9 126.5 milliseconds Electron Capture 100.00% Electron Capture with delayed Proton Emission 61.60% Electron Capture with delayed Alpha Decay 38.40% 10 19.308 seconds Electron Capture 100.00% 11 20.334 minutes Electron Capture 100.00% 12 STABLE - -

471

It's Elemental - Isotopes of the Element Rhenium  

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

Tungsten Tungsten Previous Element (Tungsten) The Periodic Table of Elements Next Element (Osmium) Osmium Isotopes of the Element Rhenium [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 185 37.40% STABLE 187 62.60% 4.33Ă—10+10 years Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 159 No Data Available No Data Available No Data Available 160 0.82 milliseconds Proton Emission 91.00% Alpha Decay 9.00% 161 0.44 milliseconds Proton Emission 100.00% Alpha Decay <= 1.40% 161m 14.7 milliseconds Alpha Decay 93.00% Proton Emission 7.00% 162 107 milliseconds Alpha Decay 94.00% Electron Capture 6.00%

472

Isotopically engineered semiconductors: from the bulk tonanostructures  

SciTech Connect

Research performed with semiconductors with controlled isotopic composition is evolving from the measurement of fundamental properties in the bulk to those measured in superlattices and nanostructures. This is driven in part by interests associated with the fields of 'spintronics' and quantum computing. In this topical review, which is dedicated to Prof. Abstreiter, we introduce the subject by reviewing classic and recent measurements of phonon frequencies, thermal conductivity, bandgap renormalizations, and spin coherence lifetimes in isotopically controlled bulk group IV semiconductors. Next, we review phonon properties measured in isotope heterostructures, including pioneering work made possible by superlattices grown by the group of Prof. Abstreiter. We close the review with an outlook on the exciting future possibilities offered through isotope control in 1, 2, and 3 dimensions that will be possible due to advances in nanoscience.

Ager III, Joel W.; Haller, Eugene E.

2006-04-07T23:59:59.000Z

473

It's Elemental - Isotopes of the Element Magnesium  

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

Sodium Sodium Previous Element (Sodium) The Periodic Table of Elements Next Element (Aluminum) Aluminum Isotopes of the Element Magnesium [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 24 78.99% STABLE 25 10.00% STABLE 26 11.01% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 19 4.0 picoseconds Double Proton Emission 100.00% 20 90.8 milliseconds Electron Capture 100.00% Electron Capture with delayed Proton Emission ~ 27.00% 21 122 milliseconds Electron Capture 100.00% Electron Capture with delayed Proton Emission 32.60% Electron Capture with delayed Alpha Decay < 0.50%

474

It's Elemental - Isotopes of the Element Chlorine  

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

Sulfur Sulfur Previous Element (Sulfur) The Periodic Table of Elements Next Element (Argon) Argon Isotopes of the Element Chlorine [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 35 75.76% STABLE 37 24.24% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 28 No Data Available Proton Emission (suspected) No Data Available 29 < 20 nanoseconds Proton Emission No Data Available 30 < 30 nanoseconds Proton Emission No Data Available 31 150 milliseconds Electron Capture 100.00% Electron Capture with delayed Proton Emission 0.70% 32 298 milliseconds Electron Capture 100.00%

475

It's Elemental - Isotopes of the Element Potassium  

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

Argon Argon Previous Element (Argon) The Periodic Table of Elements Next Element (Calcium) Calcium Isotopes of the Element Potassium [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 39 93.2581% STABLE 40 0.0117% 1.248Ă—10+9 years 41 6.7302% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 32 No Data Available Proton Emission (suspected) No Data Available 33 < 25 nanoseconds Proton Emission No Data Available 34 < 25 nanoseconds Proton Emission No Data Available 35 178 milliseconds Electron Capture 100.00% Electron Capture with delayed Proton Emission 0.37% 36 342 milliseconds Electron Capture 100.00%

476

It's Elemental - Isotopes of the Element Phosphorus  

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

Silicon Silicon Previous Element (Silicon) The Periodic Table of Elements Next Element (Sulfur) Sulfur Isotopes of the Element Phosphorus [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 31 100% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 24 No Data Available Electron Capture (suspected) No Data Available Proton Emission (suspected) No Data Available 25 < 30 nanoseconds Proton Emission 100.00% 26 43.7 milliseconds Electron Capture 100.00% Electron Capture with delayed Proton Emission No Data Available 27 260 milliseconds Electron Capture 100.00% Electron Capture with

477

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 1.139Ă—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%

478

It's Elemental - Isotopes of the Element Gallium  

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

Zinc Zinc Previous Element (Zinc) The Periodic Table of Elements Next Element (Germanium) Germanium Isotopes of the Element Gallium [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 69 60.108% STABLE 71 39.892% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 56 No Data Available Proton Emission (suspected) No Data Available 57 No Data Available Proton Emission (suspected) No Data Available 58 No Data Available Proton Emission (suspected) No Data Available 59 No Data Available Proton Emission (suspected) No Data Available 60 70 milliseconds Electron Capture 98.40%

479

It's Elemental - Isotopes of the Element Sodium  

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

Neon Neon Previous Element (Neon) The Periodic Table of Elements Next Element (Magnesium) Magnesium Isotopes of the Element Sodium [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 23 100% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 18 1.3Ă—10-21 seconds Proton Emission 100.00% 19 < 40 nanoseconds Proton Emission No Data Available 20 447.9 milliseconds Electron Capture with delayed Alpha Decay 20.05% Electron Capture 100.00% 21 22.49 seconds Electron Capture 100.00% 22 2.6027 years Electron Capture 100.00% 23 STABLE - - 24 14.997 hours Beta-minus Decay 100.00%

480

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 9Ă—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 "laser isotope separation" 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.


481

It's Elemental - Isotopes of the Element Copper  

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

Nickel Nickel Previous Element (Nickel) The Periodic Table of Elements Next Element (Zinc) Zinc Isotopes of the Element Copper [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 63 69.15% STABLE 65 30.85% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 52 No Data Available Proton Emission No Data Available 53 < 300 nanoseconds Electron Capture No Data Available Proton Emission No Data Available 54 < 75 nanoseconds Proton Emission No Data Available 55 27 milliseconds Electron Capture 100.00% Electron Capture with delayed Proton Emission 15.0% 56 93 milliseconds Electron Capture 100.00%

482

Stable isotope investigations of chlorinated aliphatic hydrocarbons.  

Science Conference Proceedings (OSTI)

Stable isotope ratio measurements for carbon (C) and chlorine (Cl) can be used to elucidate the processes affecting transformation and transportation of chlorinated aliphatic hydrocarbons (CAHs) in the environment. Methods recently developed in our laboratory for isotopic analysis of CAHs have been applied to laboratory measurements of the kinetic isotope effects associated with aerobic degradation of dichloromethane (DCM) and with both anaerobic and aerobic cometabolic degradation of trichlomethene (TCE) in batch and column microbial cultures. These experimental determinations of fractionation factors are crucial for understanding the behavior of CAHs in complex natural systems, where the extent of biotransformation can be masked by dispersion and volatilization. We have also performed laboratory investigations of kinetic isotope effects accompanying evaporation of CAHs, as well as field investigations of natural attenuation and in situ remediation of CAHs in a number of contaminated shallow aquifers at sites operated by the federal government and the private sector.

Abrajano, T.; Heraty, L. J.; Holt, B. D.; Huang, L.; Sturchio, N. C.

1999-06-01T23:59:59.000Z

483

It's Elemental - Isotopes of the Element Dysprosium  

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

Isotopes Mass Number Half-life Decay Mode Branching Percentage 138 No Data Available Electron Capture (suspected) No Data Available 139 0.6 seconds Electron Capture No Data...

484

It's Elemental - Isotopes of the Element Antimony  

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

Isotopes Mass Number Half-life Decay Mode Branching Percentage 103 1.5 microseconds Electron Capture (suspected) No Data Available 104 0.44 seconds Electron Capture 100.00%...

485

Improved process for preparing strontium-82 isotope  

DOE Patents (OSTI)

This invention is comprised of a process for making {sup 82}Sr by bombarding a molybdenum target enriched in light-mass molybdenum isotopes with high energy protons resulting in high yield, high purity {sup 82}Sr.

Michaels, G.E.; Beaver, J.E.; Moody, D.C.

1991-12-31T23:59:59.000Z

486

Laser Drilling with Gated High Power Fiber Lasers  

Science Conference Proceedings (OSTI)

About this Abstract. Meeting, Materials Science & Technology 2010. Symposium, Laser Applications in Materials Processing. Presentation Title, Laser Drilling ...

487

A characterization of separable conjugate spaces  

E-Print Network (OSTI)

Necessary and sufficient conditions for a separable Banach space to be a dual space are proved. Some applications are discussed

Rossi, Stefano

2010-01-01T23:59:59.000Z

488

Molecular Transport/Microporous Hydrogen Separation Systems  

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

Transport Microporous Hydrogen Separation Systems Participants Acquaviva, Jim: Armstrong, Tim: Asaro, Marianne: Berchtold, Kathryn: Bischoff, Brian: Cornelius, Chris: Huang,...

489