WorldWideScience

Sample records for calutrons

  1. Extraction electrode geometry for a calutron

    Science.gov (United States)

    Veach, A.M.; Bell, W.A. Jr.

    1975-09-23

    This patent relates to an improved geometry for the extraction electrode and the ground electrode utilized in the operation of a calutron. The improved electrodes are constructed in a partial-picture-frame fashion with the slits of both electrodes formed by two tungsten elongated rods. Additional parallel spaced-apart rods in each electrode are used to establish equipotential surfaces over the rest of the front of the ion source. (auth)

  2. Design of Magnetic Field System for Calutron Ion Source Set

    Institute of Scientific and Technical Information of China (English)

    REN; Xiu-yan; ZENG; Zi-qiang

    2013-01-01

    The Calutron ion source is the most important equipment of EMIS,and the structure of the ion source is more complicated.Because the parameter of each part is interrelate,as experiment and test set,It is very convenient to adjust the parameter of ion source and make the ion source get a good quality.Magnetic field system is the leading and necessary auxiliary equipment of the Calutron ion source

  3. Stable isotope separation in calutrons: Forty years of production and distribution

    Energy Technology Data Exchange (ETDEWEB)

    Bell, W.A.; Tracy, J.G.

    1987-11-01

    The stable isotope separation program, established in 1945, has operated continually to provide enriched stable isotopes and selected radioactive isotopes, including the actinides, for use in research, medicine, and industrial applications. This report summarizes the first forty years of effort in the production and distribution of stable isotopes. Evolution of the program along with the research and development, chemical processing, and production efforts are highlighted. A total of 3.86 million separator hours has been utilized to separate 235 isotopes of 56 elements. Relative effort expended toward processing each of these elements is shown. Collection rates (mg/separator h), which vary by a factor of 20,000 from the highest to the lowest (/sup 205/Tl to /sup 46/Ca), and the attainable isotopic purity for each isotope are presented. Policies related to isotope pricing, isotope distribution, and support for the enrichment program are discussed. Changes in government funding, coupled with large variations in sales revenue, have resulted in 7-fold perturbations in production levels.

  4. On the possibility of accelerating multiply charged ions in the CERN Synchrocyclotron

    CERN Document Server

    Giannini, R

    1975-01-01

    Some problems relating to the possibility of accelerating light ions in the CERN SC are studied. Deuteron capture conditions and the optimum radio-frequency versus time curve are calculated. Internal beam currents of some micro-amperes seem obtainable when using the calutron source as for protons. The same calculations were repeated for N/sup 5+/ taking into account the charge exchange process in the vacuum. A transmission of between 5 and 10% has been calculated, giving some 10/sup 10/ particles per second with a PIG source.

  5. MAGNETS

    Science.gov (United States)

    Hofacker, H.B.

    1958-09-23

    This patent relates to nmgnets used in a calutron and more particularly to means fur clamping an assembly of magnet coils and coil spacers into tightly assembled relation in a fluid-tight vessel. The magnet comprises windings made up of an assembly of alternate pan-cake type coils and spacers disposed in a fluid-tight vessel. At one end of the tank a plurality of clamping strips are held firmly against the assembly by adjustable bolts extending through the adjacent wall. The foregoing arrangement permits taking up any looseness which may develop in the assembly of coils and spacers.

  6. Clinical applications

    Science.gov (United States)

    Contributions of the Oak Ridge Calutron facility to the development and subsequent production of a majority of currently useful medical radionuclides are discussed and recommendations for future achtions presented. The role of stable isotopes in the development of radiopharmaceuticals is described. Some examples are: stable isotope molybdenum 98 for producing radiopharmaceuticals incorporating technetium 99m; thallium 203 precursor for thallium 201 which is used as tracers in the detection of coronary heart disease; and the zinc 68 precursor of gallium 67 which is used in the diagnosis of tumors and infections. The continued availability of the isotopic materials necessary for optimal health care can only be achieved by taking the following actions: (1) stocks of all the stable isotopes from which products for research and patient care are derived must be expanded and maintained; (2) all facilities, including the calutrons, capable of furnishing products to meet these needs should be identified and described; (3) federal support for the research and development of alternative separation methods should continue; and (4) an advisory committee should be created to set realistic goals, to evaluate resources, and coordinate overall efforts.

  7. Separation of selected stable isotopes by liquid-phase thermal diffusion and by chemical exchange

    Science.gov (United States)

    Rutherford, W. M.; Jepson, B. E.; Michaels, E. D.

    Useful applications of enriched stable nuclides are unduly restricted by high cost and limited availability. Recent research on liquid phase thermal diffusion (LTD) has resulted in practical processes for separating S34, CL35, and CL37 in significant quantities (100 to 500 g/yr) at costs much lower than those associated with the electromagnetic (Calutron) process. The separation of the isotopes of bromine by LTD is now in progress and BR79 is being produced in relatively simple equivalent at a rate on the order of 0.5 g/day. The results of recent measurements show that the isotopes of Zn can be separated by LTD of zinc alkyls. The isotopes of calcium can be separated by LTD and by chemical exchange. The LTD process is based on the use of aqueous Ca(NO3)2 as a working fluid.

  8. Uranium isotope separation from 1941 to the present

    Energy Technology Data Exchange (ETDEWEB)

    Maier-Komor, Peter, E-mail: Peter@Maier-Komor.d [Retired from Physik-Department E12, Technische Universitaet Muenchen, D-85747 Garching (Germany)

    2010-02-11

    Uranium isotope separation was the key development for the preparation of highly enriched isotopes in general and thus became the seed for target development and preparation for nuclear and applied physics. In 1941 (year of birth of the author) large-scale development for uranium isotope separation was started after the US authorities were warned that NAZI Germany had started its program for enrichment of uranium and might have confiscated all uranium and uranium mines in their sphere of influence. Within the framework of the Manhattan Projects the first electromagnetic mass separators (Calutrons) were installed and further developed for high throughput. The military aim of the Navy Department was to develop nuclear propulsion for submarines with practically unlimited range. Parallel to this the army worked on the development of the atomic bomb. Also in 1941 plutonium was discovered and the production of {sup 239}Pu was included into the atomic bomb program. {sup 235}U enrichment starting with natural uranium was performed in two steps with different techniques of mass separation in Oak Ridge. The first step was gas diffusion which was limited to low enrichment. The second step for high enrichment was performed with electromagnetic mass spectrometers (Calutrons). The theory for the much more effective enrichment with centrifugal separation was developed also during the Second World War, but technical problems e.g. development of high speed ball and needle bearings could not be solved before the end of the war. Spying accelerated the development of uranium separation in the Soviet Union, but also later in China, India, Pakistan, Iran and Iraq. In this paper, the physical and chemical procedures are outlined which lead to the success of the project. Some security aspects and Non-Proliferation measures are discussed.

  9. Uranium isotope separation from 1941 to the present

    Science.gov (United States)

    Maier-Komor, Peter

    2010-02-01

    Uranium isotope separation was the key development for the preparation of highly enriched isotopes in general and thus became the seed for target development and preparation for nuclear and applied physics. In 1941 (year of birth of the author) large-scale development for uranium isotope separation was started after the US authorities were warned that NAZI Germany had started its program for enrichment of uranium and might have confiscated all uranium and uranium mines in their sphere of influence. Within the framework of the Manhattan Projects the first electromagnetic mass separators (Calutrons) were installed and further developed for high throughput. The military aim of the Navy Department was to develop nuclear propulsion for submarines with practically unlimited range. Parallel to this the army worked on the development of the atomic bomb. Also in 1941 plutonium was discovered and the production of 239Pu was included into the atomic bomb program. 235U enrichment starting with natural uranium was performed in two steps with different techniques of mass separation in Oak Ridge. The first step was gas diffusion which was limited to low enrichment. The second step for high enrichment was performed with electromagnetic mass spectrometers (Calutrons). The theory for the much more effective enrichment with centrifugal separation was developed also during the Second World War, but technical problems e.g. development of high speed ball and needle bearings could not be solved before the end of the war. Spying accelerated the development of uranium separation in the Soviet Union, but also later in China, India, Pakistan, Iran and Iraq. In this paper, the physical and chemical procedures are outlined which lead to the success of the project. Some security aspects and Non-Proliferation measures are discussed.

  10. Stable isotope enrichment techniques and ORNL separation status

    Energy Technology Data Exchange (ETDEWEB)

    Tracy, J.G.; Bell, W.A.; Veach, A.M.; Caudill, H.H.; Milton, H.T.

    1987-05-01

    The isotope separation program is described, emphasizing present state-of-the-art techniques utilized to achieve specific isotopic requirements. An interesting problem addressed here is the calutron enrichment of rare-earth isotopes where small quantities of feed (<5 g) are available, and the unresolved feed is to be recovered and recycled. Conventional ion-source units using graphite and stainless steel deteriorate in the halogenating atmosphere or are permeable to rare-earth compounds, reducing the process efficiency. An ion source has been developed using boron nitride for containing the halogenating agent and rare-earth compounds. Tests have been successfully conducted using Lu/sub 2/O/sub 3/ and the in situ chlorinating technique with CCl/sub 4/. Collectively, 166 mg of /sup 176/Lu were recovered from two runs using 2.95 and 1.10 g of 44.5% /sup 176/Lu. Process efficiency of 10.5% was achieved, and 1.2 g of the unresolved feed were recovered. Material compatibility of the boron nitride, carbon tetrachloride, and lutetium compounds has been established.

  11. Stable isotope enrichment techniques and ORNL separation status

    Science.gov (United States)

    Tracy, J. G.; Bell, W. A.; Veach, A. M.; Caudill, H. H.; Milton, H. T.

    1987-05-01

    The isotope separation program is described, emphasizing present state-of-the-art techniques utilized to achieve specific isotopic requirements. An interesting problem addressed here is the calutron enrichment of rare-earth isotopes where small quantities of feed (< 5 g) are available, and the unresolved feed is to be recovered and recycled. Conventional ion-source units using graphite and stainless steel deteriorate in the halogenating atmosphere or are permeable to rare-earth compounds, reducing the process efficiency. An ion source has been developed using boron nitride for containing the halogenating agent and rare-earth compounds. Tests have been successfully conducted using Lu 2O 3 and the in situ chlorinating technique with CCl 4. Collectively, 166 mg of 176Lu were recovered from two runs using 2.95 and 1.10 g of 44.5% 176Lu. Process efficiency of 10.5% was achieved, and 1.2 g of the unresolved feed were recovered. Material compatibility of the boron nitride, carbon tetrachloride, and lutetium compounds has been established.

  12. Ion sources for energy extremes of ion implantation.

    Science.gov (United States)

    Hershcovitch, A; Johnson, B M; Batalin, V A; Kropachev, G N; Kuibeda, R P; Kulevoy, T V; Kolomiets, A A; Pershin, V I; Petrenko, S V; Rudskoy, I; Seleznev, D N; Bugaev, A S; Gushenets, V I; Litovko, I V; Oks, E M; Yushkov, G Yu; Masunov, E S; Polozov, S M; Poole, H J; Storozhenko, P A; Svarovski, A Ya

    2008-02-01

    For the past four years a joint research and development effort designed to develop steady state, intense ion sources has been in progress with the ultimate goal to develop ion sources and techniques that meet the two energy extreme range needs of meV and hundreads of eV ion implanters. This endeavor has already resulted in record steady state output currents of high charge state of antimony and phosphorus ions: P(2+) [8.6 pmA (particle milliampere)], P(3+) (1.9 pmA), and P(4+) (0.12 pmA) and 16.2, 7.6, 3.3, and 2.2 pmA of Sb(3+)Sb(4+), Sb(5+), and Sb(6+) respectively. For low energy ion implantation, our efforts involve molecular ions and a novel plasmaless/gasless deceleration method. To date, 1 emA (electrical milliampere) of positive decaborane ions was extracted at 10 keV and smaller currents of negative decaborane ions were also extracted. Additionally, boron current fraction of over 70% was extracted from a Bernas-Calutron ion source, which represents a factor of 3.5 improvement over currently employed ion sources.

  13. Molecular ion sources for low energy semiconductor ion implantation (invited)

    Energy Technology Data Exchange (ETDEWEB)

    Hershcovitch, A., E-mail: hershcovitch@bnl.gov [Brookhaven National Laboratory, Upton, New York 11973 (United States); Gushenets, V. I.; Bugaev, A. S.; Oks, E. M.; Vizir, A.; Yushkov, G. Yu. [High Current Electronics Institute, Siberian Branch of Russian Academy of Sciences, Tomsk 634055 (Russian Federation); Seleznev, D. N.; Kulevoy, T. V.; Kozlov, A.; Kropachev, G. N.; Kuibeda, R. P.; Minaev, S. [Institute for Theoretical and Experimental Physics, Moscow 117218 (Russian Federation); Dugin, S.; Alexeyenko, O. [State Scientific Center of the Russian Federation State Research Institute for Chemistry and Technology of Organoelement Compounds, Moscow (Russian Federation)

    2016-02-15

    Smaller semiconductors require shallow, low energy ion implantation, resulting space charge effects, which reduced beam currents and production rates. To increase production rates, molecular ions are used. Boron and phosphorous (or arsenic) implantation is needed for P-type and N-type semiconductors, respectively. Carborane, which is the most stable molecular boron ion leaves unacceptable carbon residue on extraction grids. A self-cleaning carborane acid compound (C{sub 4}H{sub 12}B{sub 10}O{sub 4}) was synthesized and utilized in the ITEP Bernas ion source resulting in large carborane ion output, without carbon residue. Pure gaseous processes are desired to enable rapid switch among ion species. Molecular phosphorous was generated by introducing phosphine in dissociators via 4PH{sub 3} = P{sub 4} + 6H{sub 2}; generated molecular phosphorous in a pure gaseous process was then injected into the HCEI Calutron-Bernas ion source, from which P{sub 4}{sup +} ion beams were extracted. Results from devices and some additional concepts are described.

  14. ION SOURCES FOR ENERGY EXTREMES OF ION IMPLANTATION.

    Energy Technology Data Exchange (ETDEWEB)

    HERSCHCOVITCH,A.; JOHNSON, B.M.; BATALIN, V.A.; KROPACHEV, G.N.; KUIBEDA, R.P.; KULEVOY, T.V.; KOLOMIETS, A.A.; PERSHIN, V.I.; PETRENKO, S.V.; RUDSKOY, I.; SELEZNEV, D.N.; BUGAEV, A.S.; GUSHENETS, V.I.; LITOVKO, I.V.; OKS, E.M.; YUSHKOV, G. YU.; MASEUNOV, E.S.; POLOZOV, S.M.; POOLE, H.J.; STOROZHENKO, P.A.; SVAROVSKI, YA.

    2007-08-26

    For the past four years a joint research and development effort designed to develop steady state, intense ion sources has been in progress with the ultimate goal to develop ion sources and techniques, which meet the two energy extreme range needs of mega-electron-volt and 100's of electron-volt ion implanters. This endeavor has already resulted in record steady state output currents of high charge state of Antimony and Phosphorous ions: P{sup 2+} (8.6 pmA), P{sup 3+} (1.9 pmA), and P{sup 4+} (0.12 pmA) and 16.2, 7.6, 3.3, and 2.2 pmA of Sb{sup 3+} Sb{sup 4+}, Sb{sup 5+}, and Sb{sup 6+} respectively. For low energy ion implantation our efforts involve molecular ions and a novel plasmaless/gasless deceleration method. To date, 1 emA of positive Decaborane ions were extracted at 10 keV and smaller currents of negative Decaborane ions were also extracted. Additionally, Boron current fraction of over 70% was extracted from a Bemas-Calutron ion source, which represents a factor of 3.5 improvement over currently employed ion sources.

  15. Preliminary Mark-18A (Mk-18A) Target Material Recovery Program Product Acceptance Criteria

    Energy Technology Data Exchange (ETDEWEB)

    Robinson, Sharon M. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Patton, Bradley D. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

    2016-09-01

    The U.S. Department of Energy (DOE) manages an inventory of materials that contains a range of long-lived radioactive isotopes that were produced from the 1960s through the 1980s by irradiating targets in production nuclear reactors at the Savannah River Site (SRS). One reactor was operated in a high-flux mode to produce heavy isotopes for defense purposes, DOE programmatic use, scientific research, and industrial and medical applications. In this reactor, eighty-six Mk-18A (Mk-18A) targets were subjected to long-term high neutron fluxes 47 years ago. Twentyone targets of these were processed to recover 244Pu, heavy curium (i.e., curium rich in 246-248Cm), and 252Cf. The plutonium fraction, which was rich in 244Pu, was electromagnetically enriched in the Oak Ridge National Laboratory (ORNL) calutrons to produce gram quantities of 244Pu. This high-purity 244Pu was portioned out to scientists for basic research and for nuclear nonproliferation safeguards programs. The recovered tails (designated as FP-33) contain 244Pu isotopic purities below 20% and are stored at ORNL. The processing of these 21 Mk-18A targets provided the supply of 244Pu and heavy curium in use today. The remaining 65 unprocessed targets are currently in a storage pool at SRS; they contain the world’s remaining supply of unseparated 244Pu and heavy curium.

  16. Laser Isotope Enrichment for Medical and Industrial Applications

    Energy Technology Data Exchange (ETDEWEB)

    Leonard Bond

    2006-07-01

    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".

  17. A Physicist Looks at the Terrorist Threat

    Science.gov (United States)

    Muller, Richard

    2009-05-01

    Many people fear a terrorist nuclear device, smuggled into the United States, as the one weapon that could surpass the destruction and impact of 9-11. I'll review the design of nuclear weapons, with emphasis on the kinds that can be developed by rogue nations, terrorist groups, and high-school students. Saddam, prior to the first gulf war, was developing a uranium bomb, similar to the one that destroyed Hiroshima. His calutrons (named after my university) were destroyed by the United Nations. The North Korean nuclear weapon was, like the U.S. bomb used on Nagasaki, based on plutonium. Its test released the energy equivalent of about 400 tons of TNT. Although some people have speculated that they were attempting to build a small bomb, it is far more likely that this weapon was a fizzle, with less than 1 percent of the plutonium exploded. In contrast, the energy released from burning jet fuel at the 9-11 World Trade Center attack was the equivalent of 900 tons of TNT for each plane -- over twice that of the North Korean Nuke. The damage came from the fact that gasoline delivers 10 kilocalories per gram, about 15 times the energy of an equal weight of TNT. It is this huge energy per gram that also accounts for our addiction to gasoline; per gram, high performance lithium-ion computer batteries carry only 1 percent as much energy. A dirty bomb (radiological weapon) is also unattractive to terrorists because of the threhold effect: doses less than 100 rem produce no radiation illness and will leave no dead bodies at the scene. That may be why al Qaeda instructed Jose Padilla to abandon his plans for a dirty bomb attack in Chicago, and to try a fossil fuel attack (natural gas) instead. I will argue that the biggest terrorist threat is the conventional low-tech one, such as an airplane attack on a crowded stadium using the explosive fuel that they can legally buy at the corner station.

  18. Highly Stripped Ion Sources for MeV Ion Implantation

    Energy Technology Data Exchange (ETDEWEB)

    Hershcovitch, Ady

    2009-06-30

    Original technical objectives of CRADA number PVI C-03-09 between BNL and Poole Ventura, Inc. (PVI) were to develop an intense, high charge state, ion source for MeV ion implanters. Present day high-energy ion implanters utilize low charge state (usually single charge) ion sources in combination with rf accelerators. Usually, a MV LINAC is used for acceleration of a few rnA. It is desirable to have instead an intense, high charge state ion source on a relatively low energy platform (de acceleration) to generate high-energy ion beams for implantation. This de acceleration of ions will be far more efficient (in energy utilization). The resultant implanter will be smaller in size. It will generate higher quality ion beams (with lower emittance) for fabrication of superior semiconductor products. In addition to energy and cost savings, the implanter will operate at a lower level of health risks associated with ion implantation. An additional aim of the project was to producing a product that can lead to long­ term job creation in Russia and/or in the US. R&D was conducted in two Russian Centers (one in Tomsk and Seversk, the other in Moscow) under the guidance ofPVI personnel and the BNL PI. Multiple approaches were pursued, developed, and tested at various locations with the best candidate for commercialization delivered and tested at on an implanter at the PVI client Axcelis. Technical developments were exciting: record output currents of high charge state phosphorus and antimony were achieved; a Calutron-Bemas ion source with a 70% output of boron ion current (compared to 25% in present state-of-the-art). Record steady state output currents of higher charge state phosphorous and antimony and P ions: P{sup 2+} (8.6 pmA), P{sup 3+} (1.9 pmA), and P{sup 4+} (0.12 pmA) and 16.2, 7.6, 3.3, and 2.2 pmA of Sb{sup 3+} Sb {sup 4 +}, Sb{sup 5+}, and Sb{sup 6+} respectively. Ultimate commercialization goals did not succeed (even though a number of the products like high

  19. Separation phenomena in Liquids and Gases

    Energy Technology Data Exchange (ETDEWEB)

    Louvet, P.; Dr Soubbaramayer [CEA Saclay, Dept. des Lasers et de la Physico-Chimie, DESICP/DLPC/SPP, 91 - Gif-sur-Yvette (France); Noe, P

    1989-07-01

    The Proceedings of the 1989 Workshop are presented in two volumes: volume 1 contains 4 papers on plasma processes and 7 papers on centrifugation. The papers on plasma processes deal with two main methods: ion cyclotron resonance and rotating plasmas. A survey lecture reviews extensively the physics of the two processes, the published experimental results and includes an abundant bibliography of about 200 references. The 3 other papers communicate original and recent experiments carried out by the authors. The plasma process remains as a possible technology to separate stable isotopes and isotopes of metals located in the middle of the Mendeleev Table. Regarding the stable isotopes, the ion cyclotron resonance might be an alternative to the Calutron process. The sessions on centrifugation include 2 review papers by URENCO authors and 5 specialized communications. The review papers take stock of the centrifuge research and gives the current status of the centrifuge technology in URENCO. The authors say that the centrifugation is presently an established industrial and commercial process ready to enter in competition for any new construction of enrichment capacity. Volume 2 contains the papers on 3 topics: basic studies (11 papers), chemical process (2 papers) and laser processes (7 papers). The papers on basic studies include investigations on rotating flows. A special attention is given to studies on convection flows, driven by acceleration field or (and) capillary forces. The interest of convection is obvious, as it has applications in important fields: the hydrodynamics of liquid uranium in the evaporation crucible of AVLIS Process, the crystal growth experiments on earth or under microgravity conditions (future experiments planned in space-labs) and the welding by electron or photon beams. Two papers are presented on the chemical process and both of them are by French authors. The French CEA has, in the past, developed with success the CHEMEX process. The