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Sample records for on-line isotope separator

  1. The Daresbury On-Line Isotope Separator (DOLIS)

    International Nuclear Information System (INIS)

    Grant, I.S.; Eastham, D.A.; Groves, J.; Tolfree, D.W.L.; Walker, P.M.; Green, V.R.; Rikovska, J.; Stone, N.J.; Hamilton, W.D.

    1987-01-01

    The isotope separator DOLIS, which is on-line to the Daresbury Laboratory's 20-MV tandem accelerator, is used to measure nuclear moments and decay schemes. Separated beams may be collected on a tape and transported to a counting station, implanted directly into a host lattice at on-line temperatures down to less than 10 mK, or allowed to interact with a collinear laser beam. The present status of DOLIS and its ancillary equipment is described

  2. The Daresbury on-line isotope separator (DOLIS)

    International Nuclear Information System (INIS)

    Grant, I.S.; Eastham, D.A.; Groves, J.; Tolfree, D.W.L.; Walker, P.M.; Green, V.R.; Rikovska, J.; Stone, N.J.; Hamilton, W.D.

    1987-01-01

    The isotope separator DOLIS, which is on-line to the Daresbury Laboratory's 20-MV tandem accelerator, is used to measure nuclear moments and decay schemes. Separated beams may be collected on a tape and transported to a counting station, implanted directly into a host lattice at on-line temperatures down to less than 10 mK, or allowed to interact with a collinear laser beam. The present status of DOLIS and its ancillary equipment is described. (orig.)

  3. On line isotopic separator test benches at GANIL

    International Nuclear Information System (INIS)

    Anne, R.; Bru, B.; Joubert, A.; Leroy, R.; Obert, J.; Putaux, J.C.; Liang, C.F.; Paris, P.; Orr, N.; Steckmeyer, J.C.

    1993-01-01

    A first version of isotopic separator on line test bench has been built in order to test the feasibility of the production of radioactive species from 96 MeV/u of 20 Ne impinging a thick target of MgO. This test bench was equipped with a very compact ECR ion source (Nanogan) entirely made from permanent magnets and operating at 10 Ghz. 18 Ne 2,4+ ; 19N e 1,2,3,4+ and 23,24 Ne 1+ has been produced and ionized. A new more performing separator (SIRa) allowing the use of different types of ion sources will be completed by the end of 1993. (author) 4 refs., 4 figs., 1 tab

  4. Isotopic nuclear reactor with on-line separation

    International Nuclear Information System (INIS)

    Liviu, Popa-Simil

    2007-01-01

    In the new reactor-waste cycle design the nuclear reactor gets features of the living beings - resembling the plants/vegetation -. The separation of waste starts inside the fuel by using the fission reaction to separate the fission products from the fuel. The fuel, which is preferred to be highly isotopic enriched, is fabricated in beads smaller than the fission product range, immersed in a gentle flowing liquid drain. If this liquid is Lead Bismuth (LBE) the fission products will be lighter, while in Sodium-Potassium (NaK) will be heavier, except for gases. This drain liquid will collect both the fission products and the collision damage, drawing them slow to give time to short lives disintegration chains to take place inside the shielded nuclear reactor area outside the reactor core in a separation unit. While the drain liquid with the fission products is outside the reactor core few choices are available: - To solidify the drain liquid freezing all elements inside and transport the metal in cryogenic conditions to a remote separation unit, or to apply a separation partitioning process online stabilizing and packing the fission products only, or a combination of these two. The radioactivity of this drain liquid is smaller than that of the actual used fuel because it represents the accumulation of a very short period (about 1 month or less) and had enough time to cool down all the short lives. The separation unit on-line with the nuclear reactor is composed of a density separation unit, followed by a phase interface concentration unit which moves out of the LBE the fission products as lighter impurities, and an electrochemical separation unit for the fission products. Further, chemical separation, stabilization processes are applied and the fission products are delivered partitioned on groups of chemical compatible products. Finally the specific waste is about 1 Kg/Gw*day, to which the stabilization products have to be added which increases this mass by 10 times

  5. The isotope separator on-line at the INS-SF cyclotron

    International Nuclear Information System (INIS)

    Yonehara, H.; Kawakami, H.; Tanaka, J.; Omata, K.; Shida, Y.

    1981-02-01

    The Isotope Separator On-Line at the SF Cyclotron has been improved. Some details of improvements are described on the target-ion source, rapid extraction with aluminized tape, tape transport system and data aquisition. The performance of the improved SF-ISOL is discussed. (author)

  6. On-line separation of refractory hafnium and tantalum isotopes at the ISOCELE separator

    CERN Document Server

    Liang, C F; Obert, J; Paris, P; Putaux, J C

    1981-01-01

    By chemical evaporation technique, neutron deficient hafnium nuclei have been on-line separated at the ISOCELE facility, from the isobar rare-earth elements, in the metal-fluoride HfF/sub 3//sup +/ ion form. Half-lives of /sup 162-165/Hf have been measured. Similarly, tantalum has been selectively separated on the TaF/sub 4//sup +/ form. (4 refs) .

  7. Chemical investigations of isotope separation on line target units for carbon and nitrogen beams

    CERN Document Server

    Franberg, H; Gäggeler, H W; Köster, U

    2006-01-01

    Radioactive ion beams (RIBs) are of significant interest in a number of applications. Isotope separation on line (ISOL) facilities provide RIB with high beam intensities and good beam quality. An atom that is produced within the ISOL target will first diffuse out from the target material. During the effusion towards the transfer line and into the ion source the many contacts with the surrounding surfaces may cause unacceptable delays in the transport and, hence, losses of the shorter-lived isotopes. We performed systematic chemical investigations of adsorption in a temperature and concentration regime relevant for ISOL targets and ion source units, with regard to CO/sub x/ and NOmaterials are potential construction materials for the above-mentioned areas. Off-line and on-line tests have been performed using a gas thermochromatography setup with radioactive tracers. The experiments were performed at the production of tracers for atmospheric chemistry (PROTRAC) facility at the Paul Schener Institute in Villigen...

  8. Ion source development for the on-line isotope separator at GSI

    International Nuclear Information System (INIS)

    Kirchner, R.; Burkard, K.; Hueller, W.; Klepper, O.

    1991-08-01

    The progress in the understanding of ion sources for isotope separation on-line and the feasibility of bunched beams of relatively refractory elements is reported. The ultra-high temperature FEBIAD-H ion source, facilitating the mounting of catchers and window compared to the earlier F-version, enables bunched beams of the elements with adsorption enthalpies up to almost 6 eV, e.g. of Be, Al, Ca, Cr, Fe, Co, Ni, Sr, Pd, Ba, Yb, and Au. This way also chemical selectivity for these elements may be achieved, at least to some extent, for isotopes with halflives > or approx.1 minute, including especially the difficult separation of alkaline-earth isotopes from isobaric alkalines. These studies reveal, however, also a principal difficulty in the on-line separation of refractory elements, namely their tendency, increasing with ΔH a , to re-diffuse after release from the catcher into the bulk of the hot source enclosure. (orig.)

  9. Characteristics of a gas-jet transport system for an on-line isotope separator

    International Nuclear Information System (INIS)

    Kawade, K.; Yamamoto, H.; Amano, H.; Hanada, M.; Katoh, T.; Okano, K.; Kawase, Y.; Fujiwara, I.

    1982-01-01

    Basic characteristics of a gas-jet transport system for an on-line isotope separator have been investigated using a 252 Cf source and a 235 U fission source. The transport efficiency of fission products through a capillary has been measured to be about 60% for the 235 U fission source. The sweep-out time of fission products through a target chamber and the transit time through a capillary have been measured for He, N 2 and CO 2 gases at several pressures. The measured sweep-out times have been almost equal to the exchange over time of the gas. The transit times have been found to be reasonably predicted by calculations. The transport system has been incorporated into the KUR-ISOL and is used for the study of short-lived nuclei. (orig.)

  10. The beam diagnostic instruments in Beijing radioactive ion-beam facilities isotope separator on-line

    International Nuclear Information System (INIS)

    Ma, Y.; Cui, B.; Ma, R.; Tang, B.; Chen, L.; Huang, Q.; Jiang, W.

    2014-01-01

    The beam diagnostic instruments for Beijing Radioactive Ion-beam Facilities Isotope Separator On-Line are introduced [B. Q. Cui, Z. H. Peng, Y. J. Ma, R. G. Ma, B. Tang, T. Zhang, and W. S. Jiang, Nucl. Instrum. Methods 266, 4113 (2008); T. J. Zhang, X. L. Guan, and B. Q. Cui, in Proceedings of APAC 2004, Gyeongju, Korea, 2004, http://www.jacow.org , p. 267]. For low intensity ion beam [30–300 keV/1 pA–10 μA], the beam profile monitor, the emittance measurement unit, and the analyzing slit will be installed. For the primary proton beam [100 MeV/200 μA], the beam profile scanner will be installed. For identification of the nuclide, a beam identification unit will be installed. The details of prototype of the beam diagnostic units and some experiment results will be described in this article

  11. Resonance ionization laser ion sources for on-line isotope separators (invited)

    International Nuclear Information System (INIS)

    Marsh, B. A.

    2014-01-01

    A Resonance Ionization Laser Ion Source (RILIS) is today considered an essential component of the majority of Isotope Separator On Line (ISOL) facilities; there are seven laser ion sources currently operational at ISOL facilities worldwide and several more are under development. The ionization mechanism is a highly element selective multi-step resonance photo-absorption process that requires a specifically tailored laser configuration for each chemical element. For some isotopes, isomer selective ionization may even be achieved by exploiting the differences in hyperfine structures of an atomic transition for different nuclear spin states. For many radioactive ion beam experiments, laser resonance ionization is the only means of achieving an acceptable level of beam purity without compromising isotope yield. Furthermore, by performing element selection at the location of the ion source, the propagation of unwanted radioactivity downstream of the target assembly is reduced. Whilst advances in laser technology have improved the performance and reliability of laser ion sources and broadened the range of suitable commercially available laser systems, many recent developments have focused rather on the laser/atom interaction region in the quest for increased selectivity and/or improved spectral resolution. Much of the progress in this area has been achieved by decoupling the laser ionization from competing ionization processes through the use of a laser/atom interaction region that is physically separated from the target chamber. A new application of gas catcher laser ion source technology promises to expand the capabilities of projectile fragmentation facilities through the conversion of otherwise discarded reaction fragments into high-purity low-energy ion beams. A summary of recent RILIS developments and the current status of laser ion sources worldwide is presented

  12. A chemically selective laser ion source for the on-line isotope separation

    International Nuclear Information System (INIS)

    Scheerer, F.

    1993-03-01

    In this thesis a laser ion source is presented. In a hot chamber the atoms of the elements to be studied are resonantly by light of pulsed dye lasers, which are pumped by pulsed copper-vapor lasers with extremely high pulse repetition rate (ν rep ∼ 10 kHz), stepwise excited and ionized. By the storage of the atoms in a hot chamber and the high pulse repetition rate of the copper-vapor lasers beyond the required high efficiency (ε ∼ 10%) can be reached. First preparing measurements were performed at the off-line separator at CERN with the rare earth elements ytterbium and thulium. Starting from the results of these measurements further tests of the laser ion source were performed at the on-line separator with in a thick tantalum target produced neutron-deficient ytterbium isotopes. Under application of a time-of-flight mass spectrometer in Mainz an efficient excitation scheme on the resonance ionization of tin was found. This excitation scheme is condition for an experiment at the GSI for the production of the extremely neutron-deficient, short-lived nucleus 102 Sn. In the summer 1993 is as first application of the newly developed laser ion source at the PSB-ISOLDE at CERN an astrophysically relevant experiment for the nuclear spectroscopy of the neutron-rich silver isotopes 124-129 Ag is planned. This experiment can because of the lacking selectivity of conventional ion sources only be performed by means of the here presented laser ion source. The laser ion source shall at the PSB-ISOLDE 1993 also be applied for the selective ionization of manganese. (orig./HSI) [de

  13. A four-detector spectrometer for e--γ PAC on-line with the ISOLDE-CERN isotope separator

    International Nuclear Information System (INIS)

    Marques, J.G.; Correia, J.G.; Melo, A.A.; Silva, M.F. da; Soares, J.C.

    1995-01-01

    A four-detector e - -γ spectrometer has been installed on-line with the ISOLDE isotope separator. The spectrometer consists of two magnetic lenses for detection of conversion electrons, and two BaF 2 scintillators for γ-ray detection. The spectrometer has been equipped with a 20 kV pre-acceleration system which enables detection of conversion electrons down to 2 keV. Implantation and measurement can be performed simultaneously on a large temperature range by heating or cooling the sample holder. The advantages of using the e - -γ PAC technique on-line at ISOLDE are discussed. (orig.)

  14. Very low-energy conversion electron detection (VLECED) system at the isocele on-line isotope separator, Orsay

    International Nuclear Information System (INIS)

    Kilcher, P.; Sauvage, J.; Munsch, J.; Obert, J.; Caruette, A.; Ferro, A.; Boissier, G.; Fournet-Fayas, J.; Ducourtieux, M.; Landois, G.

    1988-01-01

    A system designed and installed at the on-line isotope separator ISOCELE II allows the high resolution detection of low-energy conversion electrons (down to 1 keV) emitted by mass separated radioactive sources: the use of a special tape transport permits both the slowing down of the incoming beam of radioactive ions up to a collection point and the acceleration of the electrons emitted by the collected sources brought to a flat magnetic spectrograph. Typical spectra so obtained are presented

  15. Basic studies of a gas-jet-coupled ion source for on-line isotope separation

    International Nuclear Information System (INIS)

    Anderl, R.A.; Novick, V.J.; Greenwood, R.C.

    1980-01-01

    A hollow-cathode ion source was used in a gas-jet-coupled configuration to produce ion beams of fission products transported to it from a 252 Cf fission source. Solid aerosols of NaCl and Ag were used effectively as activity carriers in the gas-jet system. Flat-plate skimmers provided an effective coupling of the ion source to the gas jet. Ge(Li) spectrometric measurements of the activity deposited on an ion-beam collector relative to that deposited on a pre-skimmer collector were used to obtain separation efficiencies ranging from 0.1% to > 1% for Sr, Y, Tc, Te, Cs, Ba, Ce, Pr, Nd and Sm. The use of CCl 4 as a support gas resulted in a significant enhancement of the alkaline-earth and rare-earth separation efficiencies

  16. Distrinution and properties of nuclides in fission by means of on-line isotope separation

    International Nuclear Information System (INIS)

    Nir-El, Y.

    1977-07-01

    This work determines the independent yield distribution fo the alkali elements' fission products. The results were analyzed by especially developed equations and half-lives were calculated using a computer program which fits a series of exponentials to the activity decay curve by the least squares method. Independent yields were determined by use of calculated correction factors and by normalization against a known independent yield. The three nuclides 147 Ba, 148 Ba, and 149 La were indentified fot the first time in this work and their half-lives were determined Comparison with calculated values, within the framework of beta decay theory, gave in all cases agreement better than an order of magnitude. Extrapolation of the experimental curve and prediction of values which have not yet been measured are now possible. Independent yield distributions of rubidium and cesium include values for 99 Rb, 147 Cs and 148 Cs determined for the first time. The last two isotopes were identified fot the first time in the present work. A model was developed to interpretthe heavy wing phenomenon based on statistical considerations and onbasic properties of prompt neutron emission in fission. The width parameter of the independent yield distribution calculated according to the propsed model is in very good agreement with the width parameter of a Gaussian fitted to the measured distribution. (B.G.)

  17. Isotope separation

    International Nuclear Information System (INIS)

    Eerkens, J.W.

    1979-01-01

    A method of isotope separation is described which involves the use of a laser photon beam to selectively induce energy level transitions of an isotope molecule containing the isotope to be separated. The use of the technique for 235 U enrichment is demonstrated. (UK)

  18. The Eurisol report. A feasibility study for a European isotope-separation-on-line radioactive ion beam facility

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2003-12-01

    The Eurisol project aims at a preliminary design study of the next-generation European isotope separation on-line (ISOL) radioactive ion beam (RIB) facility. In this document, the scientific case of high-intensity RIBs using the ISOL method is first summarised, more details being given in appendix A. It includes: 1) the study of atomic nuclei under extreme and so-far unexplored conditions of composition (i.e. as a function of the numbers of protons and neutrons, or the so-called isospin), rotational angular velocity (or spin), density and temperature, 2) the investigation of the nucleosynthesis of heavy elements in the Universe, an important part of nuclear astrophysics, 3) a study of the properties of the fundamental interactions which govern the properties of the universe, and in particular of the violation of some of their symmetries, 4) potential applications of RIBs in solid-state physics and in nuclear medicine, for example, where completely new fields could be opened up by the availability of high-intensity RIBs produced by the ISOL method. The proposed Eurisol facility is then presented, with particular emphasis on its main components: the driver accelerator, the target/ion-source assembly, the mass-selection system and post-accelerator, and the required scientific instrumentation. Special details of these components are given in appendices B to E, respectively. The estimates of the costs of the Eurisol, construction and running costs, have been performed in as much details as is presently possible. The total capital cost (installation manpower cost included) of the project is estimated to be of the order of 630 million Euros within 20%. In general, experience has shown that operational costs per annum for large accelerator facilities are about 10% of the capital cost. (A.C.)

  19. Isotopic separation

    International Nuclear Information System (INIS)

    Castle, P.M.

    1979-01-01

    This invention relates to molecular and atomic isotope separation and is particularly applicable to the separation of 235 U from other uranium isotopes including 238 U. In the method described a desired isotope is separated mechanically from an atomic or molecular beam formed from an isotope mixture utilising the isotropic recoil momenta resulting from selective excitation of the desired isotope species by radiation, followed by ionization or dissociation by radiation or electron attachment. By forming a matrix of UF 6 molecules in HBr molecules so as to collapse the V 3 vibrational mode of the UF 6 molecule the 235 UF 6 molecules are selectively excited to promote reduction of UF 6 molecules containing 235 U and facilitate separation. (UK)

  20. Isotopic separation

    International Nuclear Information System (INIS)

    Chen, C.L.

    1979-01-01

    Isotopic species in an isotopic mixture including a first species having a first isotope and a second species having a second isotope are separated by selectively exciting the first species in preference to the second species and then reacting the selectively excited first species with an additional preselected radiation, an electron or another chemical species so as to form a product having a mass different from the original species and separating the product from the balance of the mixture in a centrifugal separating device such as centrifuge or aerodynamic nozzle. In the centrifuge the isotopic mixture is passed into a rotor where it is irradiated through a window. Heavier and lighter components can be withdrawn. The irradiated mixture experiences a large centrifugal force and is separated in a deflection area into lighter and heavier components. (UK)

  1. Isotope separation

    International Nuclear Information System (INIS)

    Bartlett, R.J.; Morrey, J.R.

    1978-01-01

    A method and apparatus is described for separating gas molecules containing one isotope of an element from gas molecules containing other isotopes of the same element in which all of the molecules of the gas are at the same electronic state in their ground state. Gas molecules in a gas stream containing one of the isotopes are selectively excited to a different electronic state while leaving the other gas molecules in their original ground state. Gas molecules containing one of the isotopes are then deflected from the other gas molecules in the stream and thus physically separated

  2. Isotopic separation

    International Nuclear Information System (INIS)

    Chen, C.L.

    1982-01-01

    A method is described for separating isotopes in which photo-excitation of selected isotope species is used together with the reaction of the excited species with postive ions of predetermined ionization energy, other excited species, or free electrons to produce ions or ion fragments of the selected species. Ions and electrons are produced by an electrical discharge, and separation is achieved through radial ambipolar diffusion, electrostatic techniques, or magnetohydrodynamic methods

  3. Efficiency of an on-line isotope separator system employing cooled and NaCl-loaded He-jet methods

    International Nuclear Information System (INIS)

    Aeystoe, J.; Rantala, V.; Valli, K.; Hillebrand, S.; Kortelahti, M.; Eskola, K.; Raunemaa, T.

    1976-01-01

    A pure helium-jet at liquid nitrogen temperature coupled to a Nielsen type ion source, and a NaCl-loaded helium-jet coupled to a hollow-cathode ion source have been investigated as means to connect a cyclotron target chamber on-line to a mass separator. Technical details and performances of some critical parts of the system are described. Total separation efficiencies measured under various experimental conditions for several nuclides vary between 0.01 and 1.0%. (Auth.)

  4. Development of an ion guide coupled to an on-line isotope separation system on Sara. Identification and study of isospin exotic nuclei at Isolde and Sara

    International Nuclear Information System (INIS)

    Bouldjedri, A.

    1992-06-01

    This work is concerned with the study of exotic nuclei located on both sides of the stability-line and known as neutron rich and neutron deficient respectively. For the former, produced by alpha particle-induced fission, an on-line isotope separation with an ion guide (IGISOL) has been developed and submitted to several off-line and on-line optimization tests showing capacity to spectroscopic studies. In the case of neutron deficient nuclei near the magicity Z=82, 182 Tl(3s) has been identified and its decaying modes and those of 183 Tl ground state, studied, using the on-line separator ISOLDE. On the other hand, the β decay of 172,175 Ir produced in 32 S induced reaction is studied using a helium jet system on the SARA accelerator. Existence of isomers is derived from half-lives measurements

  5. UWIS isotope separator

    Energy Technology Data Exchange (ETDEWEB)

    Wojtasiewicz, A. [Warsaw Univ., Inst. of Experimental Physics, Nuclear Physics Div., Warsaw (Poland)

    1997-12-31

    Since 1995 the University of Warsaw Isotope Separator group has participated in the ISOL/IGISOL project at the Heavy Ion Cyclotron. This project consists in installation of an isotope separator (on line with cyclotron heavy ion beam) with a hot plasma ion source (ISOL system) and/or with an ion guide source (IGISOL system). In the report the short description of the present status of the project is presented. 2 figs, 10 refs.

  6. This picture was taken in 1967 during the first test of the Isotope On-Line Separator (ISOLDE) installation at the 600 MeV CERN Synchro Cyclotron.

    CERN Multimedia

    CERN PhotoLab

    1967-01-01

    When ISOLDE began operation, it was unique in the world. It used a new technique to overcome the problem of rapidly separating interesting atoms from the rest of the nuclear target. Through a combination of chemical and electromagnetic methods the different isotopes were separated and converted into an ion beam made of just one isotope. On-line production of radioactive nuclei, in this way, offered many new opportunities for physicists as it allowed them to perform previously impossible experiments on short-lived nuclei. ISOLDE has become one of CERN's major installations and it supports a broad scientific programme by providing beams to different experiments. The techniques developed at ISOLDE have opened up a new field of radioactive ion-beam accelerators, both at CERN and worldwide.

  7. Development of an Ionization Scheme for Gold using the Selective Laser Ion Source at the On-Line Isotope Separator ISOLDE

    CERN Document Server

    Fedosseev, V; Marsh, B A; CERN. Geneva. AB Department

    2006-01-01

    At the ISOLDE on-line isotope separation facility, the resonance ionization laser ion source (RILIS) can be used to ionize reaction products as they effuse from the target. The RILIS process of laser step-wise resonance ionization of atoms in a hot metal cavity provides a highly element selective stage in the preparation of the radioactive ion beam. As a result, the ISOLDE mass separators can provide beams of a chosen isotope with greatly reduced isobaric contamination. The number of elements available at RILIS has been extended to 26, with the addition of a new three-step ionization scheme for gold. The optimal ionization scheme was determined during an extensive study of the atomic energy levels and auto-ionizing states of gold, carried out by means of in-source resonance ionization spectroscopy. Details of the ionization scheme and a summary of the spectroscopy study are presented.

  8. A new infiltration method for coating highly permeable matrices with compound materials for high-power isotope-separator-on-line production target applications

    International Nuclear Information System (INIS)

    Kawai, Y.; Bilheux, Jean-Christophe; Stracener, Daniel W; Alton, Gerald D

    2005-01-01

    A new infiltration coating method has been conceived for uniform and controlled thickness deposition of target materials onto highly permeable, complex-structure matrices to form short-diffusion-length isotope-separator-on-line (ISOL) production targets for radioactive ion beam research applications. In this report, the infiltration technique is described in detail and the universal character of the technique illustrated in the form of SEMs of several metal-carbide, metal-oxide and metal-sulfide targets for potential use at present or future radioactive ion beam research facilities

  9. Production of radioactive ion beams and resonance ionization spectroscopy with the laser ion source at on-line isotope separator ISOLDE

    International Nuclear Information System (INIS)

    Fedosseev, V.N.; )

    2005-01-01

    Full text: The resonance ionisation laser ion source (RILIS) of the ISOLDE on-line isotope separation facility at CERN is based on the method of laser step-wise resonance ionisation of atoms in a hot metal cavity. Using the system of dye lasers pumped by copper vapour lasers the ion beams of many different metallic elements have been produced at ISOLDE with an ionization efficiency of up to 27%. The high selectivity of the resonance ionization is an important asset for the study of short-lived nuclides produced in targets bombarded by the proton beam of the CERN Booster accelerator. Radioactive ion beams of Be, Mg, Al, Mn, Ni, Cu, Zn, Ga, Ag, Cd, In, Sn, Sb, Tb, Yb, Tl, Pb and Bi have been generated with the RILIS. Setting the RILIS laser in the narrow line-width mode provides conditions for a high-resolution study of hyperfine structure and isotopic shifts of atomic lines for short-lived isotopes. The isomer selective ionization of Cu, Ag and Pb isotopes has been achieved by appropriate tuning of laser wavelengths

  10. Solid-state Marx based two-switch voltage modulator for the On-Line Isotope Mass Separator accelerator at the European Organization for Nuclear Research.

    Science.gov (United States)

    Redondo, L M; Silva, J Fernando; Canacsinh, H; Ferrão, N; Mendes, C; Soares, R; Schipper, J; Fowler, A

    2010-07-01

    A new circuit topology is proposed to replace the actual pulse transformer and thyratron based resonant modulator that supplies the 60 kV target potential for the ion acceleration of the On-Line Isotope Mass Separator accelerator, the stability of which is critical for the mass resolution downstream separator, at the European Organization for Nuclear Research. The improved modulator uses two solid-state switches working together, each one based on the Marx generator concept, operating as series and parallel switches, reducing the stress on the series stacked semiconductors, and also as auxiliary pulse generator in order to fulfill the target requirements. Preliminary results of a 10 kV prototype, using 1200 V insulated gate bipolar transistors and capacitors in the solid-state Marx circuits, ten stages each, with an electrical equivalent circuit of the target, are presented, demonstrating both the improved voltage stability and pulse flexibility potential wanted for this new modulator.

  11. A study of some neutron-rich isotopes of lanthanum, cerium and praseodymium by means of fast chemical on-line separation technique SISAK

    International Nuclear Information System (INIS)

    Skarnemark, G.

    1977-01-01

    The fast on-line chemical separation technique SISAK has been utilized to study the decay properties of neutron-rich isotopes of La, Ce and Pr. The results include partial decay schemes and γ-ray intensity data for 14 min 143 La, 42 s 144 La, 25 s 145 La, 9 s 146 La, 3 min 145 Ce, 14 min 146 Ce, 56 s 147 Ce, 50 s 148 Ce, 12 min 147 Pr, 2 min 148 Pr, 3 min 149 Pr and 6 s 150 Pr. Half-lives and γ-ray energies are reported for the previously unknown nuclides 147 La (Tsub(1/2) = 2.2 s), 148 La (Tsub(1/2) approximately 1 s), 149 Ce (Tsub(1/2) = 5.7 s) and 150 Ce (Tsub(1/2) = 4.1 s). The nuclides were formed in thermal neutron-induced fission of 235 U. The fission products were transferred to the SISAK system via a gas jet recoil transportation (GJRT) system. The combination of the GJRT system with SISAK is discussed, as well as the chemical separation systems used for the isolation of La, Ce and Pr. The appendices I - IX contain previously published material which is included in the thesis. (Auth.)

  12. Isocele I, the Orsay synchrocyclotron on-line separator

    International Nuclear Information System (INIS)

    Caruette, A.; Ferro, A.; Foucher, R.

    1976-01-01

    The main characteristics of the isotope separator Isocele 1 are described. This medium current separator was on line with the Orsay synchrocyclotron (155 MeV p, or 210 MeV 3 He) from March 1974 up to May 1975. Results obtained with different targets (Au, Bi, Er, Pt, Sn, Th) are summarized. They confirm the efficiency of medium current separators of this type [fr

  13. Isotope separation

    International Nuclear Information System (INIS)

    Rosevear, A.; Sims, H.E.

    1985-01-01

    sup(195m)Au for medical usage is separated from sup(195m)Hg in a solution containing ions of sup(195m)Hg by contacting the solution with an adsorbing agent to adsorb 195 Hgsup(H) thereon, followed by selective elution of sup(195m)Au generated by radioactive decay of the sup(195m)Hg. The adsorbing agent comprises a composite material in the form of an inert porous inorganic substrate (e.g. Kieselguhr),the pores of which are occupied by a hydrogel of a polysaccharide (e.g. agarose) carrying terminal thiol groups for binding Hgsup(H) ions. (author)

  14. Method for separating isotopes

    International Nuclear Information System (INIS)

    Jepson, B.E.

    1976-01-01

    The invention comprises a method for separating different isotopes of elements from each other by contacting a feed solution containing the different isotopes with a macrocyclic polyether to preferentially form a macrocyclic polyether complex with the lighter of the different isotopes. The macrocyclic polyether complex is then separated from the lighter isotope depleted feed solution. A chemical separation of isotopes is carried out in which a constant refluxing system permits a continuous countercurrent liquid-liquid extraction. (LL)

  15. Method for separating isotopes

    International Nuclear Information System (INIS)

    Schlenker, R.F.

    1978-01-01

    A vortex tube for separating isotopes is described. A gas mixture containing the isotopic molecules enters the vortex tube under pressure and is separated into a hot discharge flow stream and a cold discharge flow stream. The hot discharge is enriched in lighter isotopic molecules whereas the cold discharge flow stream is enriched in the heavier isotopic molecules. The vortex tube can be used in a single stage or multistage isotope separation apparatus

  16. Method for separating isotopes

    International Nuclear Information System (INIS)

    Jepson, B.E.

    1975-01-01

    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

  17. Wide angle isotope separator

    International Nuclear Information System (INIS)

    Kantrowitz, A.

    1976-01-01

    A method and apparatus is described for particle separation. The method uses a wide angle radially expanding vapor of a particle mixture. In particular, selective ionization of one isotope type in the particle mixture is produced in a multichamber separator and the ionized isotope type is accelerated out of the path of the vapor expansion for separate collection

  18. Development of an on-line flow injection Sr/matrix separation method for accurate, high-throughput determination of Sr isotope ratios by multiple collector-inductively coupled plasma-mass spectrometry.

    Science.gov (United States)

    Galler, Patrick; Limbeck, Andreas; Boulyga, Sergei F; Stingeder, Gerhard; Hirata, Takafumi; Prohaska, Thomas

    2007-07-01

    This work introduces a newly developed on-line flow injection (FI) Sr/Rb separation method as an alternative to the common, manual Sr/matrix batch separation procedure, since total analysis time is often limited by sample preparation despite the fast rate of data acquisition possible by inductively coupled plasma-mass spectrometers (ICPMS). Separation columns containing approximately 100 muL of Sr-specific resin were used for on-line FI Sr/matrix separation with subsequent determination of (87)Sr/(86)Sr isotope ratios by multiple collector ICPMS. The occurrence of memory effects exhibited by the Sr-specific resin, a major restriction to the repetitive use of this costly material, could successfully be overcome. The method was fully validated by means of certified reference materials. A set of two biological and six geological Sr- and Rb-bearing samples was successfully characterized for its (87)Sr/(86)Sr isotope ratios with precisions of 0.01-0.04% 2 RSD (n = 5-10). Based on our measurements we suggest (87)Sr/(86)Sr isotope ratios of 0.713 15 +/- 0.000 16 (2 SD) and 0.709 31 +/- 0.000 06 (2 SD) for the NIST SRM 1400 bone ash and the NIST SRM 1486 bone meal, respectively. Measured (87)Sr/(86)Sr isotope ratios for five basalt samples are in excellent agreement with published data with deviations from the published value ranging from 0 to 0.03%. A mica sample with a Rb/Sr ratio of approximately 1 was successfully characterized for its (87)Sr/(86)Sr isotope signature to be 0.718 24 +/- 0.000 29 (2 SD) by the proposed method. Synthetic samples with Rb/Sr ratios of up to 10/1 could successfully be measured without significant interferences on mass 87, which would otherwise bias the accuracy and uncertainty of the obtained data.

  19. Separation of uranium isotopes

    International Nuclear Information System (INIS)

    Porter, J.T.

    1980-01-01

    Methods and apparatus are disclosed for separation of uranium isotopes by selective isotopic excitation of photochemically reactive uranyl salt source material at cryogenic temperatures, followed by chemical separation of selectively photochemically reduced U+4 thereby produced from remaining uranyl source material

  20. Isotope separation process

    International Nuclear Information System (INIS)

    Lyon, R.K.

    1979-01-01

    A method is described for the isotopically selective excitation of gas phase molecules by multiple infrared photon absorption after which more of the excited molecules than nonexcited molecules are converted to a chemically different form which may be separated by means known in the art. This invention is useful for, but not limited to, the separation of the principal isotopes of uranium

  1. Isotope separation process

    International Nuclear Information System (INIS)

    Lyon, R.K.

    1976-01-01

    The instant invention relates to a process for separating a material into two or more parts in each of which the abundances of the isotopes of a given element differ from the abundances of the isotopes of the same material in said material. In one embodiment, the invention relates to a method for the isotopically selective excitation of gas phase molecules by multiple infrared photon absorption followed by selective dissociation of said excited molecules by the absorption of a single photon of visible or ultraviolet light. This invention is useful for, but not limited to, the separation of the principal isotopes of uranium. 11 Claims, 2 Drawing Figures

  2. Process for isotope separation

    International Nuclear Information System (INIS)

    Emile, B.F.M.

    1983-11-01

    A process is claimed for isotopic separation applied to isotopes of elements that can be placed in at least a physicochemical form in which the isotopic atoms or the molecules containing these atoms can be easily displaced and for which there are selective radiations preferentially absorbed by the isotopes of a certain type or by the molecules containing them, said absorption substantially increasing the probability of ionization of said atoms or molecules relative to the atoms or molecules that did not absorb the radiation. The process consists of placing the isotopic mixture in such a form, subjecting it in a separation zone to selective radiations and to an electrical field that produces migration of positive ions toward the negative electrodes and negative ions toward the positive electrodes, and withdrawing from certain such zones the fractions thus enriched in certain isotopes

  3. Isotope separation process

    International Nuclear Information System (INIS)

    1976-01-01

    The invention relates to a process for separating a given material into two or more parts, in each of which the abundances of the isotopes of a given element differ from the abundances of the isotopes of the same material in the said material. More particularly, the invention relates to a method for the isotopically selective excitation of gas phase UF 6 by infrared photon absorption followed by selective reaction of said excited UF 6 with atomic chlorine, bromine, or iodine to form a product which may be separated by means known in the art

  4. Radiation gradient isotope separator

    International Nuclear Information System (INIS)

    Hughes, J.L.

    1980-01-01

    A system is described for transporting, separating and storing charged particles, charged antiparticles and fully or partially ionized isotopes of any element comprising a laser beam generator, laser beam intensity profiler, a laser beam variable intensity attenuator, and means for injecting charged particles, charged antiparticles and ionized isotopes into the beam and extracting them from the system as required. The invention is particularly useful for channelling electrons and ions used for fuel pellet compression in inertial fusion systems, for separating the isotopes of elements and for the confinement of charged antiparticles and particle/antiparticle plasmas

  5. Isotope separation process

    International Nuclear Information System (INIS)

    Lyon, R.K.

    1977-01-01

    The instant invention relates to a process for separating a material into two or more parts in each of which the abundances of the isotopes of a given element differ from the abundances of the isotopes of the same material in said material. More particularly, the invention relates to a method for the isotopically selective excitation of gas phase molecules by multiple infrared photon absorption followed by a step wherein more of the excited molecules than nonexcited molecules are converted to a chemically different form which may be separated by means known in the art. This invention is useful for, but not limited to, the separation of the principal isotopes of uranium. 15 claims, 1 figure

  6. Isotope separation process

    International Nuclear Information System (INIS)

    Thomas, W.R.L.

    1979-01-01

    The instant invention relates to an improved process for separating a material into two or more parts in each of which the abundances of the isotopes of a given element differ from the abundances of the isotopes of the same element in said material. More particularly, the invention relates to a method for the isotopically selective excitation of gas phase molecules by multiple infrared photon absorption followed by a step wherein more of the excited molecules than non-excited molecules are converted to a chemically different form which may be separated by means known in the art. This invention is useful for, but not limited to, the separation of the principal isotopes of uranium

  7. Process for isotope separation

    International Nuclear Information System (INIS)

    Schuster, E.; Kersting, A.; Gebauhr, W.

    1980-01-01

    Isotope separation in UF 6 gas takes place on the principle of selective excitation by laser irradiation and separation by chemical conversion with a partner in a reaction. Atomic H, N or O or the CH 3 or CHO radicals are suitable partners in the reaction. The recombination takes place by catalytic acceleration on leaving the reaction area. (DG) [de

  8. Isotope separation process

    International Nuclear Information System (INIS)

    Cox, D.M.; Maas, E.T.

    1982-01-01

    Processes are disclosed for the separation of isotopes of an element comprising vaporizing uranyl compounds having the formula (UO2a2)n, where a is a monovalent anion and n in an integer from 2 to 4, the compounds having an isotopically shifted infrared absorption spectrum associated with uranyl ions containing said element which is to be separated, and then irradiating the uranyl compound with infrared radiation which is preferentially absorbed by a molecular vibration of uranyl ions of the compound containing a predetermined isotope of that element so that excited molecules of the compound are provided which are enriched in the molecules of the compound containing that predetermined isotope, thus enabling separation of these excited molecules. The processes disclosed include separation of the excited molecules by irradiating under conditions such that the excited molecules dissociate, and also separating the excited molecules by a discrete separation step. The latter includes irradiating the excited molecules by a second infrared laser in order to convert the excited molecules into a separable product, or also by chemically converting the excited molecules, preferably by reaction with a gaseous reactant

  9. Laser isotope separation

    International Nuclear Information System (INIS)

    1976-01-01

    The claimed invention is a method of isotope separation based on the unimolecular decomposition of vibrationally excited negative ions which are produced in the reaction of thermal electrons and molecules which have been vibrationally excited in an isotope selective manner. This method is especially applicable to molecules represented by the formula MF 6 wherein M is selected from the group consisting of U, S, W, Se, Te, Mo, Re and Tc

  10. Laser isotope separation process

    International Nuclear Information System (INIS)

    Kaldor, A.

    1976-01-01

    The claimed invention is a method of isotope separation based on the unimolecular decomposition of vibrationally excited negative ions which are produced in the reaction of thermal electrons and molecules which have been vibrationally excited in an isotope selective manner. This method is especially applicable to molecules represented by the formula MF 6 wherein M is selected from the group consisting of U, S, W, Se, Te, Mo, Re, and Tc. 9 claims, 1 drawing figure

  11. High mass isotope separation arrangement

    International Nuclear Information System (INIS)

    Eerkens, J.W.

    1980-01-01

    This invention relates to the isotope separation art and, more particularly, to a selectively photon-induced energy level transition of an isotopic molecule containing the isotope to be separated and a chemical reaction with a chemically reactive agent to provide a chemical compound containing atoms of the isotope desired. In particular a description is given of a method of laser isotope separation applied to the separation of 235 UF 6 from 238 UF 6 . (U.K.)

  12. Isotope separation process

    International Nuclear Information System (INIS)

    Wexler, Sol; Young, C.E.

    1976-01-01

    Description is given of method for separating a specific isotope from a mixture of isotopes of an actinide element present as MF 6 , wherein M is the actinide element. It comprises: preparing a feed gas mixture of MF 6 in a propellant gas; passing the feed gas mixture under pressure through an expansion nozzle while heating the mixture to about 600 0 C; releasing the heated gas mixture from the nozzle into an exhaust chamber having a reduced pressure, whereby a gas jet of MF 6 molecules, MF 6 molecular clusters and propellant gas molecules is formed, the MF 6 molecules having a translational energy of about 3 eV; converting the MF 6 molecules to MF 6 ions by passing the jet through a cross jet of electron donor atoms so that an electron transfer takes place between the MF 6 - molecules and the electron donor atoms whereby the jet is now quasi-neutral, containing negative MF 6 - ions and positive donor ions; passing the quasi-neutral jet through a radiofrequency mass filter tuned to separate the MF 6 ions containing the specific isotope from the MF 6 - ions of the other isotopes and neutralizing and collecting the MF 6 molecules of the specific isotope [fr

  13. Isotope separation apparatus

    International Nuclear Information System (INIS)

    Lyon, R.K.; Eisner, P.N.; Thomas, W.R.I.

    1983-01-01

    This application discloses a method for and an apparatus in which isotopes of an element in a compared are separated from each other while that compound, i.e., including a mixture of such isotopes, flows along a predetermined path. The apparatus includes a flow tube having a beginning and an end. The mixture of isotopes is introduced into the flow tube at a first introduction point between the beginning and the end thereof to flow the mixture toward the end thereof. A laser irradiates the flow tube dissociating compounds of a preselected one of said isotopes thereby converting the mixture in an isotopically selective manner. The dissociation products are removed from the tube at a first removal point between the first introduction point and the end. The dissociation product removed at the the first removal point are reconverted back into the comound thereby providing a first stage enriched compound. This first stage enriched compound is reintroduced into the flow tube at a second introduction point between the beginning thereof and the first introduction point. Further product is removed from the flow tube at a second removal point between the second introduction point and the first introduction point. The second introduction point is chosen so that the isotope composition of the first stage enriched compound is approximately the same as that of the compound in the flow tube

  14. Chromatographic hydrogen isotope separation

    International Nuclear Information System (INIS)

    Aldridge, F.T.

    1983-01-01

    Intermetallic compounds with the CaCu5 type of crystal structure, particularly LaNiCo and CaNi5, exhibit high separation factors and fast equilibrium times and therefore are useful for packing a chromatographic hydrogen isotope separation column. The addition of an inert metal to dilute the hydride improves performance of the column. A large scale multi-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

  15. Chromatographic hydrogen isotope separation

    International Nuclear Information System (INIS)

    Aldridge, F.T.

    1981-01-01

    Intermetallic compounds with the CaCu5 type of crystal structure , particularly LaNiCo and CaNi5, 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

  16. Method to separate isotopes

    International Nuclear Information System (INIS)

    Coenen, H.; Neuschuetz, D.

    1980-01-01

    An extraction by means of supercritical pure gases (e.g. CD 2 ) or gas mixtures is proposed to separate isotopes, especially H/D, Li-6/Li-7, and U-235/U-238, and water or benzol is used as entrainer. The extraction shall be carried out at pressure rates of about 350 bar above the critical pressure with the temperature being by up to 100 0 C above the critical temperature. A NaCl-solution and the change of the isotopic ratio Cl-35/Cl-37 are investigated for example purpose. (UWI) [de

  17. Isotope separation process

    International Nuclear Information System (INIS)

    Cabicar, J.; Stamberg, K.; Katzer, J.

    1983-01-01

    A process for separating isotopes by the method of controlled distribution is claimed. A first phase is either a solution of isotopic components and a ligand (from 10 - 6 M to a saturated solution), or a gaseous mixture of isotopic components, or a gaseous mixture of isotopic components and an inert gas. The isotopes are in the starting mixture in molar ratio from 1:10 5 to 1:10 - 5 . The second phase is a solid sorbent such as styrene-divinylbenzene ion exchangers, or bio-sorbents on the basis of mycelium of lower fungi and sorbents on the basis of cellulose, or an extraction agent such as tributyl phosphate and trioctyl amine, if need be, kept by a carrier such as teflon, silica gel and cellulose. The two-phase system exhibits non-linear equilibrium isotherm for sorption and/or desorption or for extraction and/or re-extraction. After bringing both phases into contact the rate of transport of isotopic components from one phase into another is not equal. Retardation of isotopic exchange takes place by complexation of isotopes with ligands such as cabonate, sulphate, citrate, chloride and ethylenediamine tetraacetate ions, or by using sorbents and extraction agents with chelating functional groups such as carboxyl and hyroxyl groups, groups on the basis of phosphorus, nitrogen and sulphur and/or by operating in darkness, or in the light having wave length between 2.5x10 2 and 10 9 nm. The contact time is between 10 - 2 and 10 6 s, temperature between 10 2 and 10 3 K, the number of stirrer revolutions between 10 - 2 and 10 4 revolutions per s, flow rate at column arrangement between 10 - 6 and 10 - 1 m/s and the size of particles of sorbent between 10 - 6 and 10 - 2 m

  18. Isotope separation system

    International Nuclear Information System (INIS)

    Lehmann, J.-C.

    1975-01-01

    A description is given of an isotope separation device comprising a system for converting into gaseous form a first and second isotope to be separated, a monochromatic excitation light source to excite the gaseous molecules of these two isotopes in a distinct manner, a first and second receiver to collect selectively the molecules of the first and second distinctly excited isotopes. The frequency FL of the excitation light is selected between a lower limit and a higher limit F2 + 1/2 LD, depending on the frequences F1 and F2 of two absorption lines near this first and second isotope. The difference DF between these two frequencies F1 and F2 is less than the Doppler width LD of each one of these lines and greater than the natural width LN of each of these two lines and also the width of line LR of the excitation light source. The probability that the molecules will be excited by this light depends on the direction of their displacement to a major and different extent for both isotopes. An ionising light source LI is set up to irradiate the seat of interaction between the excitation light and the gaseous molecules with an ionisation light able to ionise the excited molecules without ionising the molecules that are not excited. The receivers are able to collect selectively the ionised molecules. A sufficiently low gas pressure is selected for the distance between the place of interaction and the first receiver to be less than double the free mean travel of the molecules in the gas [fr

  19. On-line mass separator of superheavy atoms

    International Nuclear Information System (INIS)

    Oganesyan, Yu.Ts.

    2002-01-01

    The concept is presented of an on-line Mass Analyzer of SuperHeavy Atoms (MASHA) dedicated to the separation and determination of the mass and decay properties of new elements and isotopes produced in heavy-ion induced reactions. The new nuclides with half-lives T 1/2 ≥ 1 s are transported to an ECR-source working at a frequency of 2.45 GHz and are separated by mass with a mass resolution of M/ΔM ∼ 1500. In the focal plane of the magnetic analyzer a front strip detector surrounded by side detectors will be placed to determine the mass according to the signals from the detected α-particles or fission fragments with efficiency of about 90 %. In comparison to other existing in-flight recoil separators, the present setup will be characterized by higher efficiency and high selectivity relative to background reaction products. The setup MASHA may be used also in the investigation of nuclear reactions of different type induced by stable and radioactive beams

  20. On-Line Mass Separator of Superheavy Atoms

    CERN Document Server

    Oganessian, Yu T

    2002-01-01

    The concept is presented of an on-line Mass Analyzer of SuperHeavy Atoms (MASHA) dedicated to the separation and determination of the mass and decay properties of new elements and isotopes produced in heavy-ion induced reactions. The new nuclides with half-lives T_{1/2}\\ge 1 s are transported to an ECR-source working at a frequency of 2.45 GHz and are separated by mass with a mass resolution of M/\\Delta M\\sim 1500. In the focal plane of the magnetic analyzer a front strip detector surrounded by side detectors will be placed to determine the mass according to the signals from the detected alpha-particles or fission fragments with efficiency of about 90 %. In comparison to other existing in-flight recoil separators, the present setup will be characterized by higher efficiency and high selectivity relative to background reaction products. The setup MASHA may be used also in the investigation of nuclear reactions of different type induced by stable and radioactive beams.

  1. Isotope separation process

    International Nuclear Information System (INIS)

    Kaldor, A.; Rabinowitz, P.

    1979-01-01

    A method of separating the isotopes of an element is described, which comprises the steps of (i) subjecting molecules of a gaseous compound of the element simultaneously to two infrared radiations of different wavelengths, the first radiation having a wavelength which corresponds to an absorption band of the compound, which in turn corresponds to a mode of molecular motion in which there is participation by atoms of the element, and the second radiation having a power density greater than 10 6 watts per cm 2 , thereby exciting molecules of the compound in an isotopically selective manner, this step being conducted in such manner that the excited molecules either receive a level of energy sufficient to cause them to undergo conversion by unimolecular decomposition or receive a level of energy sufficient to cause them to undergo conversion by reaction with molecules of another gas present for that purpose; and (ii) separating and recovering converted molecules from unconverted molecules. (author)

  2. Laser separation of uranium isotopes

    International Nuclear Information System (INIS)

    Porter, J.T.

    1981-01-01

    Method and apparatus for separating uranium isotopes are claimed. The method comprises the steps of irradiating a uranyl source material at a wavelength selective to a desired isotope and at an effective temperature for isotope spectral line splitting below about 77 deg.K., further irradiating the source material within the fluorescent lifetime of the source material to selectively photochemically reduce the excited isotopic species, and chemically separating the reduced isotope species from the remaining uranyl salt compound

  3. Method of isotope separation

    Energy Technology Data Exchange (ETDEWEB)

    Lyon, R K

    1975-05-22

    Isotopes of a gaseous compound can be separated by multi-infrared photoabsorption which follows a selective dissociation of the excited molecules by single photon absorption of photons of visible or UV radiation. The process involves three steps. Firstly, the molecules to be separated are irradiated with a high-energy IR laser, whereby the molecules of the compound containing the lighter isotopes are preferably excited. They are then irradiated by a second laser with UV or visible light whose frequency of radiation brings the excited molecules into a form in which they can be separated from the non-excited molecules. The third step is the reformation of the substances according to known methods. A power density of at least 10/sup 4/ watt/cm/sup 2/ per torr gas pressure with an irradiation time of 10/sup -10/ to 5 x 10/sup -5/ seconds in the presence of a second gas with at least 5 times higher partial pressure is necessary for the IR radiation. The method may be used for UF/sub 6/ for which an example is given here.

  4. Isotope separation process

    International Nuclear Information System (INIS)

    Lyon, R.K.; Kaldor, A.

    1977-01-01

    In a method for the separation of isotopes of uranium in UF 6 , the UF 6 is subjected to ir radiation at a predetermined wavelength or set of wavelengths for less than 10 -3 sec in such a manner that at least 0.1% of the 235 UF 6 molecules absorb an energy of more than 2000 cm -1 . The excited UF 6 is then reacted with a gaseous reagent, F 2 , Cl 2 , or Br 2 , to produce a product which is then recovered by means known in the art

  5. High mass isotope separation arrangement

    International Nuclear Information System (INIS)

    Eerkens, J.W.

    1976-01-01

    An isotope separation arrangement for separating a preselected isotope from a mixture of chemically-identical but isotopically-different molecules by either photon-induced pure revibrational or vibronic selective excitation of the molecules containing the atoms of the isotope to be separated from a lower to a higher energy state, and a chemical reaction of the higher energy state molecules with a chemically-reactive agent to form a chemical compound containing primarily the atoms of the isotope to be separated in a physicochemical state different from the physicochemical state of the mixture of chemically-identical but isotopically-different molecules. The chemical compound containing the atoms of the isotope to be separated may be subsequently processed to obtain the isotope. The laser configuration used to generate the photon beam is fully described

  6. Advanced isotope separation

    International Nuclear Information System (INIS)

    1982-01-01

    The Study Group briefly reviewed the technical status of the three Advanced Isotope Separation (AIS) processes. It also reviewed the evaluation work that has been carried out by DOE's Process Evaluation Board (PEB) and the Union Carbide Corporation-Nuclear Division (UCCND). The Study Group briefly reviewed a recent draft assessment made for DOE staff of the nonproliferation implications of the AIS technologies. The staff also very briefly summarized the status of GCEP and Advanced Centrifuge development. The Study Group concluded that: (1) there has not been sufficient progress to provide a firm scientific, technical or economic basis on which to select one of the three competing AIS processes for full-scale engineering development at this time; and (2) however, should budgetary restraints or other factors force such a selection, we believe that the evaluation process that is being carried out by the PEB provides the best basis available for making a decision. The Study Group recommended that: (1) any decisions on AIS processes should include a comparison with gas centrifuge processes, and should not be made independently from the plutonium isotope program; (2) in evaluating the various enrichment processes, all applicable costs (including R and D and sales overhead) and an appropriate discounting approach should be included in order to make comparisons on a private industry basis; (3) if the three AIS programs continue with limited resources, the work should be reoriented to focus only on the most pressing technical problems; and (4) if a decision is made to develop the Atomic Vapor Laser Isotope Separation process, the solid collector option should be pursued in parallel to alleviate the potential program impact of liquid collector thermal control problems

  7. Laser assisted aerodynamic isotope separation

    International Nuclear Information System (INIS)

    Berg, H. van den

    1985-01-01

    It is shown that the efficiency of conventional aerodynamic isotope seperation can be improved by two orders of magnitude with the aid of a relatively weak cw infrared laser which is used to induce isotopically selective condensation. Overall isotope enrichment factors in excess of 2 are obtained as compared to about 1.02 in the conventional seperation. Sulphur isotopes in SF 6 as well as Silicon isotopes in SiF 4 and Bromine isotopes in CF 3 Br are seperated on a laboratory scale. Infrared vibrational predissociation by itself and in combination with isotopically selective condensation are also shown to be effective new ways of isotope separation. (orig.) [de

  8. Isotope separation using tunable lasers

    International Nuclear Information System (INIS)

    Snavely, B.B.

    1975-01-01

    Various processes for laser isotope separation based upon the use of the spectroscopic isotope effect in atomic and molecular vapors are discussed. Emphasis is placed upon processes which are suitable for uranium enrichment. A demonstration process for the separation of uranium isotopes using selective photoionization is described. (U.S.)

  9. Separation of uranium isotopes

    International Nuclear Information System (INIS)

    Ehrfeld, W.; Ehrfeld, U.

    1977-01-01

    In the nuclear fuel cycle, uranium enrichment is not a principal problem of technological feasibility. Several processes exist for producing LWR fuel and the enrichment method can be selected in consideration of economical, environmental, and political aspects. To date, the gaseous diffusion process constitutes the major part of enrichment capacity. This process has been well demonstrated for over 30 years and, as a matter of fact, no major technological and economical progress is to be expected in the future. Because of their comparatively high development potential, the centrifuge and the separation nozzle method may become increasingly favorable in economics. The development of the centrifuge process which is superior by its low specific energy consumption aims at technological improvements. In the separation nozzle process which offers the advantage of a comparatively simple technology a further reduction of the specific energy consumption is to be expected because of the thermodynamically favorable separation mechanism of this process. Laser isotope separation methods are still on the laboratory scale, although large financial funds have been spent. (orig.) [de

  10. Zirconium isotope separation process

    International Nuclear Information System (INIS)

    Peterson, S.H.; Lahoda, E.J.

    1988-01-01

    A process is described for reducing the amount of zirconium 91 isotope in zirconium comprising: forming a first solution of (a) a first solvent, (b) a scavenger, and (c) a zirconium compound which is soluble in the first solvent and reacts with the scavenger when exposed to light of a wavelength of 220 to 600 nm; irradiating the first solution with light at the wavelength for a time sufficient to photoreact a disproportionate amount of the zirconium compound containing the zirconium 91 isotope with the scavenger to form a reaction product in the first solution; contacting the first solution, while effecting the irradiation, with a second solvent which is immiscible with the first solvent, which the second solvent is a preferential solvent for the reaction product relative to the first solvent, such that at least a portion of the reaction product is transferred to the second solvent to form a second solution; and separating the second solution from the first solution after the contacting

  11. Isotopic separation by ion chromatography

    International Nuclear Information System (INIS)

    Albert, M.G.; Barre, Y.; Neige, R.

    1994-01-01

    The isotopic exchange reaction and the isotopic separation factor are first recalled; the principles of ion chromatography applied to lithium isotope separation are then reviewed (displacement chromatography) and the process is modelled in the view of dimensioning and optimizing the industrial process; the various dimensioning parameters are the isotopic separation factor, the isotopic exchange kinetics and the material flow rate. Effects of the resin type and structure are presented. Dimensioning is also affected by physico-chemical and hydraulic parameters. Industrial implementation features are also discussed. 1 fig., 1 tab., 5 refs

  12. Dielectrophoretic separation of gaseous isotopes

    International Nuclear Information System (INIS)

    McConnell, D.B.

    1975-01-01

    Gaseous isotopes are separated from a mixture in a vertically elongated chamber by subjecting the mixture to a nonuniform transverse electric field. Dielectrophoretic separation of the isotopes is effected, producing a transverse temperature gradient in the chamber, thereby enhancing the separation by convective countercurrent flow. In the example given, the process and apparatus are applied to the production of heavy water from steam

  13. Isotope separation method and apparatus

    International Nuclear Information System (INIS)

    Lyon, R.K.; Eisner, P.N.; Thomas, W.R.L.

    1980-01-01

    A method and apparatus are specified for separating a mixture of isotopes present in a compound, preferably a gaseous compound, into two or more parts in each of which the abundances of the isotopes differ from the natural abundances of the isotopes in the compound. The invention particularly relates to carrying out a laser induced, isotopically selective conversion of gaseous molecules in such a manner as to achieve more than one stage of isotope separation along the length of the laser beam. As an example, the invention is applied to the separation of the isotopes of uranium in UF 6 , in which either the U-235 or U-238 isotope is selectively excited by means of irradiation from an infrared laser, and the selectively excited isotope converted into a product that can be recovered from UF 6 by one of a variety of methods that are described. (U.K.)

  14. ITER isotope separation system

    International Nuclear Information System (INIS)

    Busigin, A.; Sood, S.K.; Kveton, O.K.; Sherman, R.H.; Anderson, J.L.

    1990-09-01

    This document presents the results of a study that examined the technical operating and economic viability of an alternative Isotope Separation System (ISS) design based on the distributed design concept. In the distributed design, the ISS is broken up into local independently operable subsystems matched to local processing requirements. The distributed design accepts the same feeds and produces essentially the same products as the reference design. The distributed design consists of two separate, independent subsystems. The first, called ISS-H, receives only protium-dominated streams and waste water from tritium extraction. It has two cryogenic distillation columns and can produce a 50 percent D, 50 percent T product since it lacks D/T separation capability. A final 80 percent T 2 concentration product can be obtained by blending the 50 percent T 2 stream from ISS-H with the more than 99 percent T 2 stream from the second subsystem, ISS-D. The second subsystem receives only deuterium-dominated feeds, which also contain some protium. ISS-D is as complex as the reference design, but smaller. Although each subsystem has some advantages, such as only two cryogenic distillation columns in ISS-H and better than 99 percent steady state T 2 product in ISS-D, the combined subsystems do not offer any real advantage compared to the reference IISS. The entire distributed ISS design has been simulated using Ontario Hydro's FLOSHEET steady state process simulator. Dynamic analysis has not been done for the distributed design. (10 refs., 3 figs., 8 tabs.)

  15. Advances in laser isotope separation

    International Nuclear Information System (INIS)

    Herman, I.P.; Bernhardt, A.F.

    1988-01-01

    The physical and chemical concepts required to understand laser isotope separation are presented and discussed. The numerous successful demonstrations of separating isotopes using lasers are reviewed to 1983. Emphasis is placed on the separation of 235-U from 238-U by multi-step selective ioniation of uranium atomic vapor, and on the separation of D and H and of T from D, by pulsed infrared laser multiple-photon dissociation of fluoroform and chloroform, respectively, because they are among the most successful and important examples of laser isotope separation to date. 161 refs.; 7 figs

  16. Can the waiting-point nucleus 78Ni be studied at an on-line mass-separator?

    Science.gov (United States)

    Wöhr, A.; Andreyev, A.; Bijnens, N.; Breitenbach, J.; Franchoo, S.; Huyse, M.; Kudryavtsev, Y. A.; Piechaczek, A.; Raabe, R. R.; Reusen, I.; Vermeeren, L.; Van Duppen, P.

    1997-02-01

    Short-lived nickel isotopes have been studied using a chemically selective Ion Guide Laser Ion Source (IGLIS) based on resonance ionisation of atoms at the Leuven Isotope Separator On-Line (LISOL) separator. The decay properties of different Ni isotopes have been studied using β-γ-coincidences. Experimental production rates of proton induced fission of 238U are obtained for 69,71Ni. These numbers are in a strong disagreement with Silberg-Tsao calculations.

  17. Dielectrophoretic separation of gaseous isotopes

    International Nuclear Information System (INIS)

    McConnell, D.B.

    1976-01-01

    This invention relates to a process for the separation of gaseous isotopes by electrophoresis assisted by convective countercurrent flow and to an apparatus for use in the process. The invention is especially applicable to heavy water separation from steam; however, it is to be understood that the invention is broadly applicable to the separation of gaseous isotopes having different dipole moments and/or different molecular weights. (author)

  18. Isotope separation by ion waves

    International Nuclear Information System (INIS)

    Dawson, J.M.

    1978-01-01

    One of the isotopes of an element having several isotopes can be separated from the others in a dense, neutral plasma. Thus initially a neutral plasma is prepared including the element in question. This may consist of positive ions and negative electrons or alternatively of positive and negative ions, or else of a mixture of positive ions, negative ions and electrons. The plasma may then be injected into a magnetic field or may be generated in the field where more energy is imparted to a selected isotope than to the others. Finally, the isotopes are separated from each other on the basis of their differential energies. For example, the selected isotope may be given more energy than the others by stimulating it within the plasma at its resonant frequency which may be close to the cyclotron frequency, either by an electric field or by a magnetic field. In order to excite the other isotope, a different resonant frequency is required which depends on the plasma density, the relative concentration of electrons if the plasma contains electrons, the strength of the magnetic field, the ratio of charge to mass of the isotope, and possibly on the physical parameters of the plasma apparatus itself, such as the ratio of the length of the plasma column to its radius. The more energetic isotope may be separated by energy dependent chemical reactions, it may be collected by a positively biased probe or else the isotopes may be separated from each other by magnetic fields or in various other ways

  19. Isotope separation by magnetic fields

    International Nuclear Information System (INIS)

    Dawson, J.M.

    1978-01-01

    One of the isotopes of an element having several isotopes can be separated from the others in a dense, neutral plasma. Thus initially a neutral plasma is prepared including the element in question. This may consist of positive ions and negative electrons or alternatively of positive and negative ions, or else of a mixture of positive ions, negative ions and electrons. The plasma may then be injected into a magnetic field or may be generated in the field where more energy is imparted to a selected isotope than to the others. Finally, the isotopes are separated from each other on the basis of their differential energies. For example, the selected isotope may be given more energy than the others by stimulating it within the plasma at its resonant frequency which may be close to the cyclotron frequency, either by an electric field or by a magnetic field. In order to excite the other isotope, a different resonant frequency is required which depends on the plasma density, the relative concentration of electrons if the plasma contains electrons, the strength of the magnetic field, the ratio of charge to mass of the isotope, and possibly on the physical parameters of the plasma apparatus itself, such as the ratio of the length of the plasma column to its radius. The more energetic isotope may be separated by energy dependent chemical reactions, it may be collected by a positively biased probe or else the isotopes may be separated from each other by magnetic fields or in various other ways

  20. Method for separating krypton isotopes

    International Nuclear Information System (INIS)

    Porter, J.T.

    1980-01-01

    Methods and apparatus for separating krypton isotopes utilizing low temperature selective infrared excitation of 85krypton difluoride in an isotopic compound mixture. Multiphoton ir excitation and uv excitation techniques are used, as well as cryogenic matrix isolation and inert buffer gas isolation techniques

  1. High atomic weight isotope separator

    International Nuclear Information System (INIS)

    Book, D.L.

    1978-01-01

    A continuously operating device is described which separates one isotopic species of a given element from a mixture. The given element is vaporized and formed into a neutral beam containing the isotopes desired to be separated. The plasma is accelerated through a laser beam which is formed by two separate lasers which operate in the continuous wave mode in which the beams are as nearly as possible in the same beam path. The two laser output beams excite and ionize the isotope of interest while leaving the remaining atoms unaffected. The ionized isotopes are then separated from the beam by an electrostatic deflection technique and the unaffected atoms continue on in their path and are directed to a recovery device

  2. Chemical separation of boron isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Palko, A.A.

    1978-06-01

    This is the final report of the research performed at ORNL on the chemical fractionation of boron isotopes between BF/sub 3/ gas and the liquid molecular addition compounds of BF/sub 3/. Thirty compounds were studied, ten of them in detail. Graphs and equations are given for variation of isotopic equilibrium constant, vapor pressure, and BF/sub 3/ solubility as a function of temperature. Rate of isotopic exchange and melting points were determined. Several of the compounds are likely candidates for use in a gas-liquid countercurrent exchange system for large-scale separation of boron isotopes. 23 figs, 53 tables, 39 references.

  3. Chemical separation of boron isotopes

    International Nuclear Information System (INIS)

    Palko, A.A.

    1978-06-01

    This is the final report of the research performed at ORNL on the chemical fractionation of boron isotopes between BF 3 gas and the liquid molecular addition compounds of BF 3 . Thirty compounds were studied, ten of them in detail. Graphs and equations are given for variation of isotopic equilibrium constant, vapor pressure, and BF 3 solubility as a function of temperature. Rate of isotopic exchange and melting points were determined. Several of the compounds are likely candidates for use in a gas-liquid countercurrent exchange system for large-scale separation of boron isotopes. 23 figs, 53 tables, 39 references

  4. Deuterium isotope separation

    International Nuclear Information System (INIS)

    Benson, S.W.

    1979-01-01

    Deuterium-containing molecules are separated and enriched by exposing commercially available ethylene, vinyl chloride, 1,2-dichloroethane or propylene to the radiation of tuned infrared lasers to selectively decompose these compounds into enriched molecular products containing deuterium atoms. The deuterium containing molecules can be easily separated from the starting material by absorption, distillation or other simple chemical separation techniques and methods. After evaporation such deuterium containing molecules can be burned to form water with an enriched deuterium content or pyrolyzed to form hydrogen gas with an enriched deuterium content. (author)

  5. Isotope separation by standing waves

    International Nuclear Information System (INIS)

    Altshuler, S.

    1984-01-01

    The separation of isotopes is accomplished by scattering a beam of particles from a standing electromagnetic wave. The particles may consist of either atoms or molecules, the beam having in either case a desired isotope and at least one other. The particle beam is directed so as to impinge on the standing electromagnetic wave, which may be a light wave. The particles, that is, the atomic or molecular quantum-mechanical waves, see basically a diffraction grating corresponding to the troughs and peaks of the electromagnetic wave. The frequency of the standing electromagnetic wave substantially corresponds to an internal energy level-transition of the desired isotope. Accordingly, the desired isotope is spatially separated by being scattered or diffracted. (author)

  6. Lasers for isotope separation

    International Nuclear Information System (INIS)

    O'Hair, E.A.; Piltch, M.S.

    1976-01-01

    The Los Alamos Scientific Laboratory is conducting research on uranium enrichment. All processes being studied employ uranium molecules and use lasers to provide isotopic selectivity and enrichment. There are four well-defined infrared frequencies and two ultraviolet frequency bands of interest. The infrared frequencies are outside the range of the available lasers and an extensive research and development activity is currently underway. Lasers are available in the uv bands, however, much development work remains. The specification for the commercial uranium enrichment plant lasers will depend upon the results of the current enrichment experiments, the laser capital cost, reliability, and maintenance cost. For the processes under investigation there are specific photon requirements but latitude in how these requirements can be met. The final laser selections for the pilot plant need not be made until the mid-1980's. Between now and that time as extensive as possible a research and development effort will be maintained

  7. Isotope separator laoratory development

    International Nuclear Information System (INIS)

    Anderl, R.A.

    1977-01-01

    Significant improvements in the capability for collection of mass-separated ions are described. These improvements centered on the fabrication and installation of a more versatile collection-beam viewing system and the design, fabrication, installation and testing of a retardation lens. A summary description of this capability development is presented

  8. Stable isotopes - separation and application

    International Nuclear Information System (INIS)

    Lockhart, I.M.

    1980-01-01

    In this review, methods used for the separation of stable isotopes ( 12 C, 13 C, 14 N, 15 N, 16 O, 17 O, 18 O, 34 S) will be described. The synthesis of labelled compounds, techniques for detection and assay, and areas of application will also be discussed. Particular attention will be paid to the isotopes of carbon, nitrogen, and oxygen; to date, sulphur isotopes have only assumed a minor role. The field of deuterium chemistry is too extensive for adequate treatment; it will therefore be essentially excluded. (author)

  9. Lithium isotopic separation: preliminary studies

    International Nuclear Information System (INIS)

    Macedo, Sandra Helena Goulart de

    1998-01-01

    In order to get the separation of natural isotopes of lithium by electrolytic amalgamation, an electrolytic cell with a confined mercury cathode was used to obtain data for the design of a separation stage. The initial work was followed by the design of a moving mercury cathode electrolytic cell and three experiments with six batches stages were performed for the determination of the elementary separation factor. The value obtained, 1.053, was ill agreement: with the specialized literature. It was verified in all experiments that the lithium - 6 isotope concentrated in the amalgam phase and that the lithium - 7 isotope concentrated in the aqueous phase. A stainless-steel cathode for the decomposition of the lithium amalgam and the selective desamalgamation were also studied. In view of the results obtained, a five stages continuous scheme was proposed. (author)

  10. Separation process for boron isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Rockwood, S D

    1975-06-12

    The method according to the invention is characterized by the steps of preparing a gaseous mixture of BCl/sub 3/ containing the isotopes of boron and oxygen as the extractor, irradiating that mixture in the tube of the separator device by means of P- or R-lines of a CO/sub 2/ laser for exciting the molecules containing a given isotope of boron, simultaneously irradiating the mixture with UV for photodissociating the excited BCl/sub 3/ molecules and separating BCl/sub 3/ from the reaction products of photodissociation and from oxygen. Such method is suitable for preparing boron used in nuclear reactors.

  11. Isotope separation apparatus and method

    International Nuclear Information System (INIS)

    Feldman, B. J.

    1985-01-01

    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

  12. Isotope separations using chromatographic methods

    International Nuclear Information System (INIS)

    Leseticky, L.

    1985-01-01

    A survey is given of chromatographic separations of compounds only differing in isotope composition. Isotope effects on physical properties which allow chromatographic separation (vapour tension, adsorption heat, partition coefficient) are very small, with the exception of the simplest molecules. Therefore, separation factors only assume the value of several per cent. From this ensues the necessity of using columns which are specially and very carefully prepared and have a separation efficiency of the order of 10 4 theoretical plates. Briefly discussed is liquid chromatography on ion exchangers which with a varied degree of success was used for separating simple inorganic compounds or ions. Ion exchange chromatography of amino acids labelled with tritium, and chromatography of tritium labelled steroids also provided only a certain degree of separation. A detailed analysis is presented of gas chromatography separation of various deuterium and tritium labelled low-molecular compounds, to which a number of studies has been devoted in the literature. Very promising is the method of complexation gas chromatography based on the reversible formation of a complex of the ligand (the compound being separated) and the compound of the (transition) metal as the steady-state phase. (author)

  13. Isotope separation apparatus and method

    International Nuclear Information System (INIS)

    Cotter, T.P.

    1982-01-01

    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

  14. Atomic vapor laser isotope separation

    International Nuclear Information System (INIS)

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

    1985-01-01

    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

  15. High mass isotope separation process and arrangement

    International Nuclear Information System (INIS)

    Eerkens, J.W.

    1978-01-01

    An isotope separation arrangement for separating a preselected isotope from a mixture of chemically identical but isotopically different molecules by either photon-induced pure rovibrational or vibronic selective excitation of the molecules containing the atoms of the isotope to be separated from a lower to a higher energy state, and a chemical reaction of the higher energy state molecules with a chemically reactive agent to form a chemical compound containing primarily the atoms of isotope to be separated in a physicochemical state different from the physicochemical state of the mixture of chemically identical but isotopically different molecules. The chemical compound containing the atoms of the isotope to be separated may be subsequently processed to obtain the isotope

  16. Status and prospects of isotope separation industry

    International Nuclear Information System (INIS)

    Safutin, V.D.; Verbin, Yu.V.; Tolstoj, V.V.

    2000-01-01

    The stages of the separation industry in the USSR and Russia are demonstrated. The current status of the separation industry and state of the equipment of the isotope separation plants are noted. The developed program for the modernization of the uranium isotope separation involves the production of perspective gas centrifuges, the improvements in the works of gas centrifuge plants and construction materials [ru

  17. Method for separating gaseous mixtures of isotopes

    International Nuclear Information System (INIS)

    Neimann, H.J.; Schuster, E.; Kersting, A.

    1976-01-01

    A gaseous mixture of isotopes is separated by laser excitation of the isotope mixture with a narrow band of wavelengths, molecularly exciting mainly the isotope to be separated and thereby promoting its reaction with its chemical partner which is excited in a separate chamber. The excited isotopes and the chemical partner are mixed, perhaps in a reaction chamber to which the two excited components are conducted by very short conduits. The improvement of this method is the physical separation of the isotope mixture and its partner during excitation. The reaction between HCl and the mixture of 238 UF 6 and 235 UF 6 is discussed

  18. Separation of uranium isotopes by accelerated isotope exchange reactions

    International Nuclear Information System (INIS)

    Seko, M.; Miyake, T.; Inada, K.; Ochi, K.; Sakamoto, T.

    1977-01-01

    A novel catalyst for isotope exchange reaction between uranium(IV) and uranium(VI) compounds enables acceleration of the reaction rate as much as 3000 times to make industrial separation of uranium isotopes economically possible

  19. Isotope separation using vibrationally excited molecules

    International Nuclear Information System (INIS)

    1979-01-01

    This invention relates to isotope separation employing isotopically selective vibrational excitation and vibration-translation reactions of the excited particles. Uranium enrichment, using uranium hexafluoride, is a particular embodiment. (U.K.)

  20. Method and device for isotope separation

    International Nuclear Information System (INIS)

    Dawson, J.M.

    1976-01-01

    The method works with a converted Q machine. The plasma containing the isotopes to be separated is crossed by a magnetic field running in the direction of the plasma column. More energy is transfered to the chosen isotope by oscillating magnetic and/or electric fields or by sound waves by using the specific resonance frequency for the selected isotope. The isotopes thus heated to different extents can be separated according to various methods given in the patent claims. (GG) [de

  1. Atomic and molecular isotope separation

    International Nuclear Information System (INIS)

    Melamed, N.T.

    1979-01-01

    A method for differentially exciting a selected isotopic species in a mixture of isotopic species is described characterized in that almost the entire isotopic mixture is placed in an excited gaseous state; and a preselected isotopic species is then selectively de-excited through stimulated emission

  2. Isotope separation by rotating plasmas

    International Nuclear Information System (INIS)

    Nicoli, C.

    1982-02-01

    A steady-state model of a fully ionized plasma column in a concentric cylindrical electrodes structures is proposed to study the plasma separation properties of its singly ionized ionic species, composed of two isotopes of the element. In this model (a one-fluid model) rotation is imparted to the plasma column through the J (vector) x B (vector) interaction. Radial pressure balance is mainly between the radial component of the J (vector) x B (vector) force and the pressure gradient plus centrifugal force and the azimutal component of the J (vector) x B (vector) force is balanced purely by viscous force. A pressure tensor 31 describes the viscoys effect and the heat balance provides an equation for temperature. A uranium gas with is two main isotopes (U 235 and U 238 ) was used for the ionic component of the plasma. The computing code to solve the resulting, system of equations in tems of density, temperature, and velocity as functions of the radial independent variable was set up to yield solutions satisfying null velocity conditions on both boundaries (inner and outer electrodes). (M.A.F.) [pt

  3. Atomic lithium vapor laser isotope separation

    CERN Document Server

    Olivares, I E

    2002-01-01

    An atomic vapor laser isotope separation in lithium was performed using tunable diode lasers. The method permits also the separation of the isotopes between the sup 6 LiD sub 2 and the sup 7 LiD sub 1 lines using a self-made mass separator which includes a magnetic sector and an ion beam designed for lithium. (Author)

  4. Atomic lithium vapor laser isotope separation

    International Nuclear Information System (INIS)

    Olivares, I.E.; Rojas, C.

    2002-01-01

    An atomic vapor laser isotope separation in lithium was performed using tunable diode lasers. The method permits also the separation of the isotopes between the 6 LiD 2 and the 7 LiD 1 lines using a self-made mass separator which includes a magnetic sector and an ion beam designed for lithium. (Author)

  5. Gas isotope separation method using plasma sheet

    International Nuclear Information System (INIS)

    Takayama, K.; Takagi, K.; Fukvi, R.

    1988-03-01

    A high frequency electric field is applied to a plasma sheet with a frequency equal to the cyclotronic frequency of the ions to be separated. Because of resonance the cyclotronic radius of the isotope has increased and the electric charge is eliminated by collision with a separator and the isotope is separated in neutral particles [fr

  6. On-line stable isotope measurements during plant and soil gas exchange

    International Nuclear Information System (INIS)

    Yakir, D.

    2001-01-01

    Recent techniques for on-line stable isotope measurements during plant and soil exchange of CO 2 and/or water vapor are briefly reviewed. For CO 2 , these techniques provide means for on-line measurements of isotopic discrimination during CO 2 exchange by leaves in the laboratory and in the field, of isotopic discrimination during soil respiration and during soil-atmosphere CO 2 exchange, and of isotopic discrimination in O 2 during plant respiration. For water vapor, these techniques provide means to measure oxygen isotopic composition of water vapor during leaf transpiration and for the analysis of sub microliter condensed water vapor samples. Most of these techniques involve on-line sampling of CO 2 and water vapor from a dynamic, intact soil or plant system. In the laboratory, these systems also allow on-line isotopic analysis by continuous-flow isotope ratio mass spectrometry. The information obtained with these on-line techniques is becoming increasingly valuable, and often critical, for ecophysiologial research and in the study of biosphere-atmosphere interactions. (author)

  7. Development of Separation Materials Containing Palladium for Hydrogen Isotopes Separation

    International Nuclear Information System (INIS)

    Deng Xiaojun; Luo Deli; Qian Xiaojing

    2010-01-01

    Displacement chromatography (DC) is a ascendant technique for hydrogen isotopes separation. The performance of separation materials is a key factor to determine the separation effect of DC. At present,kinds of materials are researched, including palladium materials and non-palladium materials. It is hardly replaceable because of its excellent separation performance, although palladium is expensive. The theory of hydrogen isotopes separation using DC was introduced at a brief manner, while several palladium separation materials were expatiated in detail(Pd/K, Pd-Al 2 O 3 , Pd-Pt alloy). Development direction of separation materials for DC was forecasted elementarily. (authors)

  8. Safeguards implications of laser isotope separation

    International Nuclear Information System (INIS)

    Moriarty, T.F.; Taylor, K.

    1993-10-01

    The purpose of this report is to describe and emphasise the safeguards and relevant features of atomic vapour laser isotope separation (AVLIS) and molecular laser isotope separation (MLIS), and to consider the issues that must be addressed before a safeguards approach at a commercial AVLIS or MLIS facility can be implemented. (Author)

  9. Laser photochemical separation of hydrogen isotopes

    International Nuclear Information System (INIS)

    Fowler, M.C.

    1979-01-01

    A method of separating isotopes of hydrogen utilizing isotopically selective photodissociation of organic acid is disclosed. Specifically acetic or formic acid containing compounds of deuterated nd hydrogenated acid is irradiated by radiation having a wavelength in the infrared spectrum between 9.2 to 10.8 microns to produce deuterium hydroxide and deuterium hydride respectively. Maintaining the acid at an elevated temperature significantly improves the yield of isotope separation

  10. Sulfur and selenium isotope separation by distillation

    International Nuclear Information System (INIS)

    Mills, T. R.; McInteer, B. B.; Montoya, J. G.

    1988-01-01

    Sulfur and selenium isotopes are used for labeled compounds and as precursors for radioisotope production; however, both limited availability and high costs are problems. A new method is needed for large-scale separation of these isotopes. Experimental distillation columns were used to measure isotopic separations for sulfur and selenium compounds. The maximum total isotope separation of 32 S vs. 34 S were 1.127 for H 2 S, 1.048 for COS, 0.838 for SF 4 , and 1.058 for CH 3 SH. Relative volatilities of 32 S vs. 34 S are 1.0006 for COS and 0.9976 for SF 4 . There is a reverse isotope effect for carbon in COS. No isotopic separation was observed for dimethyl selenide. The lower mass selenium isotopes in H 2 Se are more volatile. Distillation is a promising method for separating sulfur isotopes on a production scale. Existing distillation technology produced separated isotopes with an effect similar to that found for sulfur in SF 4 . 8 refs., 2 tabs

  11. Sulfur and selenium isotope separation by distillation

    International Nuclear Information System (INIS)

    Mills, T.R.; McInteer, B.B.; Montoya, J.G.

    1989-01-01

    Sulfur and selenium isotopes are used for labeled compounds and as precursors for radioisotope production; however, both limited availability and high costs are problems. A new method is needed for large-scale separation of theses isotopes. Experimental distillation columns were used to measure isotopic separations for sulfur and selenium compounds. The maximum total isotope separations of 32 S vs. 34 S were 1.127 for H 2 S, 1.048 for COS, 0.838 for SF 4 , and 1.058 for CH 3 SH. Relative volatilities of 32 S and 34 S are 1.0006 for COS and 0.9976 for SF 4 . There is a reverse isotope effect for carbon in COS. No isotopic separation was observed for dimethyl selenide. The lower mass selenium isotopes in H 2 Se are more volatile. Distillation is a promising method for separating sulfur isotopes on a production scale. Existing distillation technology produces separated isotopes with an effect similar to that found for sulfur in SF 4 . (author). 8 refs.; 2 tabs

  12. Amalgam-chromatographic separation of magnesium isotopes

    International Nuclear Information System (INIS)

    Klinskij, G.D.; Levkin, A.V.; Ivanov, S.A.

    1990-01-01

    Separation of magnesium isotopes within Mg(Hg)-MgI 2 system (in dimethylformamide) is conducted under amalgam-chromatographic conditions. Separation maximal degree, that is (1.09), for 24 Mg and 26 Mg and separation coefficient (α = 1.0089±0.006) are determined. Light isotopes are found to concentrate in the amalgam. Technique of thermal conversion of flows within amalgam-dimethylformamide system is suggested on the basis of reversible reaction of Ca-Mg element exchange

  13. Method and apparatus for separating isotopes

    International Nuclear Information System (INIS)

    Harris, S.E.

    1976-01-01

    Isotope separation is achieved between species A and B having an absorption resonance separated by an isotopic shift by selectively exciting a portion of species A using a tunable photon source of narrow emission line with and subsequently causing collisions with an optically excited third species to selectively ionize the excited portion of species A. When ionized, species A is easily separated by any technique, using its ionized condition to distinguish it from species B. 18 claims, 3 drawing figures

  14. Isotope separation by ionic cyclotron resonance

    International Nuclear Information System (INIS)

    Compant La Fontaine, A.; Gil, C.; Louvet, P.

    1986-10-01

    The principle of the process of isotopic separation by ionic cyclotron resonance is explained succinctly. The theoretical calculation of the isotopic effect is given as functions of the electric and magnetic fields in the frame of single particle approximation and of plasma collective theory. Then, the main parts of the demonstration device which is in operation at the CEA, are described here: the supraconducting magnetic field, the used diagnostics, the principle of the source and the collecting apparatus. Some experimental results are given for chromium. The application of the process to ponderal separation of metal isotopes, as chromium, nickel and molybdenum is discussed in view of production of medical, structural and irradiation isotopes

  15. Uranium isotope separation using styrene cation exchangers

    International Nuclear Information System (INIS)

    Kahovec, J.

    1980-01-01

    The separation of 235 U and 238 U isotopes is carried out either by simple isotope exchange in the system uranium-cation exchanger (sulphonated styrene divinylbenzene resin), or by combination of isotope exchange in a uranium-cation exchanger (Dowex 50, Amberlite IR-120) system and a chemical reaction. A review is presented of elution agents used, the degree of cation exchanger cross-linking, columns length, and 235 U enrichment. The results are described of the isotope effect study in a U(IV)-U(VI)-cation exchanger system conducted by Japanese and Romanian authors (isotope exchange kinetics, frontal analysis, reverse (indirect) frontal analysis). (H.S.)

  16. Isotope effect and isotope separation. A chemist's view

    International Nuclear Information System (INIS)

    Ishida, Takanobu

    2002-01-01

    What causes the isotope effects (IE)? This presentation will be centered around the equilibrium isotope effects due to the differences in the nuclear masses. The occurrence of the equilibrium constant, K, of isotope exchange reactions which differ from the values predicted by the classical theory of statistical mechanics, K cl , is explored. The non-classical K corresponds to the unit-stage separation factor, α, that is different from unity and forms a basis of an isotope separation process involving the chemical exchange reaction. Here, the word 'chemical exchange' includes not only the isotope exchange chemical reactions between two or more chemical species but also the isotope exchanges involving the equilibria between liquid and vapor phases and liquid-gas, liquid solution-gas, liquid-liquid, and solid-liquid phases. In Section I, origins of the isotope effect phenomena will be explored and, in the process, various quantities used in discussions of isotope effect that have often caused confusions will be unambiguously defined. This Section will also correlate equilibrium constant with separation factor. In Section II, various forms of temperature-dependence of IE and separation factor will be discussed. (author)

  17. Method for isotope separation by photodeflection

    International Nuclear Information System (INIS)

    Bernhardt, A.F.

    1977-01-01

    In the method of separating isotopes wherein a desired isotope species is selectively deflected out of a beam of mixed isotopes by irradiating the beam with a directed beam of light of narrowly defined frequency which is selectively absorbed by the desired species, the improvement comprising irradiating the deflected beam with light from other light sources whose frequencies are selected to cause the depopulation of any metastable excited states

  18. Separation unit for uranium isotopes etc

    International Nuclear Information System (INIS)

    1975-01-01

    The task of the invention - improving the efficiency of a uranium isotope separation unit with a rotor as separation chamber by improving its flow characteristics - is solved by a central-axial gas conduction system with radial branches which leads the media into the separation chambers or out of these. (UWI) [de

  19. Installation of an isotope separator in Debrecen

    International Nuclear Information System (INIS)

    Gacsi, Z.; Gulyas, J.; Vitez, A.; Csige, L.; Krasznahorkay, A.

    2005-01-01

    Complete text of publication follows. An isotope separator named OSIRIS was decommissioned in Studsvik, Sweden last July. Researchers there offered this equipment to us for dismantling and moving it over to ATOMKI in Debrecen for installation at the cyclotron lab and save and use it in nuclear physics and other sciences where stable and radioactive isotopes are used extensively for fundamental and applied research. Since the separator was used to separate radioactive isotopes, the ion source with its beam extracting, shaping, and transporting accessories, as well as the lining inside the bending magnet, furthermore the beam diagnostic and shaping elements in the 'switchyard' part of the separator had to stay in Studsvik because of the high radioactive contamination. In order to operate this equipment, first we have to design and manufacture these parts together with a new endstation for the collection and handling of the separated isotopes. Parallel with the installation, we also concentrate on different applications of an isotope separator, including separation of stable isotopes for labelling special compounds used in many branches of sciences, medical care, and industry, and on studying single ion implantation possibilities, as well as on the production of special targets for nuclear physics research. First we want to separate stable isotopes, and then, when we overcome all technical pitfalls, we will consider using this equipment to separate radioactive isotopes as well. Our intention is to have this equipment available to anyone at ATOMKI and elsewhere interested in using its capabilities in their own research fields. Consequently, all comments, suggestion, and ideas are welcome now and continuously, since the design and manufacture of parts can then be oriented by taking into account all the suggestions as much as possible. (author)

  20. Nuclear orientation of on-line separated isotopes

    International Nuclear Information System (INIS)

    Vanneste, L.; Vandeplassche, D.; Walle, E. van; Geenen, J.; Nuytten, C.; Marshak, H.

    1981-01-01

    The purpose of nuclear orientation in the study of nuclei far from stability is explained. Various methods of nuclear orientation are compared. The Leuven setup and its initial performance are described. (orig.)

  1. Nuclear yield determinations using isotope-separator-on-line arrangements

    International Nuclear Information System (INIS)

    Rudstam, G.

    1975-01-01

    The delay between the formation of a nuclear reaction product and its collection in front of measuring equipment in ISOL arrangements using integrated target-ion source systems has been analyzed. It is shown that a typical delay function takes the form const x (1-esup(-γt))esup(-μt) with γ >> μ. The results can be used for decay corrections in nuclear yield determinations. (Auth.)

  2. Separation of calcium isotopes with cryptand complexes

    International Nuclear Information System (INIS)

    Heumann, K.G.; Schiefer, H.P.

    1981-01-01

    The calcium isotope separation in the liquid-liquid extraction system H 2 O/CHCl 3 is investigated using and cryptands for complex formation as well as without complexing agent. An extraction procedure is used which allows the transfer of larger amounts of calcium in the H 2 O phase. Without complexing agent in the extraction system, enrichment of the lighter calcium isotopes is already evident in the CHCl 3 phase which is just the same as when using cryptand. In the case of cryptand as a complexing agent, the isotope separation is higher. The separation factor is calculated to be a = 1 + epsilon = 1.011 for 40 Ca/ 48 Ca without complexing agent or with cryptand and a = 1.015 in the system with cryptand. For 40 Ca/ 44 Ca the epsilon-value is smaller by nearly a factor of two. These separation factors are the highest which are determined in chemical systems for calcium isotopes. (orig.)

  3. Possible application of laser isotope separation

    International Nuclear Information System (INIS)

    Delionback, L.M.

    1975-05-01

    The laser isotope separation process is described and its special economic features discussed. These features are its low cost electric power operation, capital investment costs, and the costs of process materials. (Author)

  4. Laser isotope separation studies in JAERI

    International Nuclear Information System (INIS)

    Arisawa, Takashi; Shiba, Koreyuki

    1986-01-01

    For uranium enrichment, Japan Atomic Energy Research Institute (JAERI) has been studying atomic vapor laser isotope separation since 1976, in addition to such separation methods as gas diffusion, chemical exchange and gas-dynamic techniques. Studies carried out to date in JAERI is briefly summarized in the first part of the report. Then, some major separation techniques which have been studied in JAERI are outlined, and typical results obtained are presented. A large part is devoted to the multiple-photon photoionization technique, which is commonly known as the atomic laser isotope separation method for uranium enrichment. It has such advantages as 1) very high spectral selectivity for the relevant isotope and 2) highly improved photoionizing effect by means of two- and three-step resonance photoionization processes. Here, the atomic laser isotope separation method is discussed in detail with respect to the evaporation process, energy levels, photoionization, selectivity, photoionization schemes, ion recovery, separation in macroscopic amounts, and separation of trace amounts of isotopes. Typical observed and claculated results related to these subjects are shown. In addition, the report briefly describes some other separation processes including laser induced chemical reaction, multiple photo-dissociation, multiple-photo excitation and UV dissociation, laser induced thermal diffusion, and laser centrifugation. (Nogami, K.)

  5. Separation of nitrogen isotopes by laser light

    Energy Technology Data Exchange (ETDEWEB)

    Izawa, Y; Noguchi, Y; Yamanaka, C [Osaka Univ., Suita (Japan). Faculty of Engineering

    1976-06-01

    The separation experiment on nitrogen isotopes by laser light was made. First, the nitrogen isotopes of /sup 14/N and /sup 15/N in NH/sub 3/ molecules were separated by CO/sub 2/ laser and UV light. The separation factor and the enrichment factor were calculated. It was shown that their pressure dependence was in good agreement with the measured values. The separation factor of about 2% was obtained with UV light of 10/sup 6/W/cm/sup 2/.

  6. Isotope separation using vibrationally excited molecules

    International Nuclear Information System (INIS)

    Woodroffe, J.A.; Keck, J.C.

    1977-01-01

    A system for isotope separation or enrichment wherein molecules of a selected isotope type in a flow of molecules of plural isotope types are vibrationally excited and collided with a background gas to provide enhanced diffusivity for the molecules of the selected isotope type permitting their separate collection. The system typically is for the enrichment of uranium using a uranium hexafluoride gas in combination with a noble gas such as argon. The uranium hexafluoride molecules having a specific isotope of uranium are vibrationally excited by laser radiation. The vibrational energy is converted to a translation energy upon collision with a particle of the background gas and the added translation energy enhances the diffusivity of the selected hexafluoride molecules facilitating its condensation on collection surfaces provided for that purpose. This process is periodically interrupted and the cryogenic flow halted to permit evaporation of the collected molecules to provide a distinct, enriched flow

  7. Stable isotope separation by thermal diffusion

    International Nuclear Information System (INIS)

    Vasaru, Gheorghe

    2001-01-01

    Thermal diffusion in both gaseous and liquid phase has been subject of extensive experimental and theoretical investigations, especially after the invention of K. Clusius and G. Dickel of the thermal diffusion column, sixty three years ago. This paper gives a brief overview of the most important research and developments performed during the time at the National Institute for Research and Development for Isotopic and Molecular Technology (ITIM) at Cluj - Napoca, Romania in the field of separation of stable isotopes by thermal diffusion. An retrospective analysis of the research and results concerning isotope separation by thermal diffusion entails the following conclusions: - thermal diffusion is an adequate method for hydrogen isotope separation (deuterium and tritium) and for noble gas isotope separation (He, Ne, Ar, Kr, Xe); - thermal diffusion is attractive also for 13 C enrichment using methane as raw material for separation, when annual yields of up to 100 g are envisaged; - lately, the thermal diffusion appears to be chosen as a final enrichment step for 17 O. An obvious advantage of this method is its non-specificity, i.e. the implied equipment can be utilized for isotope separation of other chemical elements too. Having in view the low investment costs for thermal diffusion cascades the method appears economically attractive for obtaining low-scale, laboratory isotope production. The paper has the following content: 1. The principle of method; 2. The method's application; 3. Research in the field of thermal diffusion at ITIM; 4. Thermal diffusion cascades for N, C, Ne, Ar and Kr isotope separation; 5. Conclusion

  8. Hydrogen isotope separation by cryogenic distillation method

    International Nuclear Information System (INIS)

    Hayakawa, Nobuo; Mitsui, Jin

    1987-01-01

    Hydrogen isotope separation in fusion fuel cycle and tritium recovery from heavy water reactor are very important, and therefore the early establishment of these separation techniques are desired. The cryogenic distillation method in particular is promising for the separation of hydrogen isotope and the recovery of high concentrated tritium. The studies of hydrogen isotope separation by cryogenic distillation method have been carried out by using the experimental apparatus made for the first time in Japan. The separation of three components (H 2 -HD-D 2 ) under total reflux conditions was got by using the packing tower of 500 mm height. It was confirmed that the Height Equivalent Theoretical Plate (HETP) was 20 - 30 mm for the vapor's line velocity of 20 - 80 mm/s. (author)

  9. Production of chemically reactive radioactive ion beams through on-line separation

    International Nuclear Information System (INIS)

    Joinet, A.

    2003-10-01

    The ISOL (isotope separation on line) allows the production of secondary radioactive ion beams through spallation or fragmentation or fission reactions that take place in a thick target bombarded by a high intensity primary beam. The challenge is to increase the intensity and purity of the radioactive beam. The optimization of the system target/source requires the right choice of material for the target by taking into account the stability of the material, its reactivity and the ionization method used. The target is an essential part of the system because radioactive elements are generated in it and are released more or less quickly. Tests have been made in order to select the best fitted material for the release of S, Se, Te, Ge and Sn. Materials tested as target filling are: ZrO 2 , Nb, Ti, V,TiO 2 , CeO x , ThO 2 , C, ZrC 4 and VC). Other molecules such as: COSe, COS, SeS, COTe, GeS, SiS, SnS have been studied to ease the extraction of recoil nuclei (Se, S, Te, Ge and Sn) produced inside the target

  10. Isotope separation by photoselective dissociative electron

    International Nuclear Information System (INIS)

    Stevens, C.G.

    1978-01-01

    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 is described. 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, 235 UF 6 is separated from a UF 6 mixture by selective excitation followed by dissociative electron capture into 235 UF 5 - and F

  11. New aspects of uranium isotope separation

    International Nuclear Information System (INIS)

    Leonhardt, W.; Mueller, G.

    1979-01-01

    The need of 235 U enrichment capacity is discussed on the basis of the requirements for nuclear power in the next 10 ... 20 years. In this connection, the performance of gas diffusion, of the gas centrifuge and of the separation nozzle method are compared with each other, and an evaluation of the optical methods of isotope separation is given. (author)

  12. Laser separation of isotopes of hydrogen

    International Nuclear Information System (INIS)

    Dave, S.M.; Ghosh, S.K.; Sadhukhan, H.K.

    1980-01-01

    Laser isotope separation technique is explained and various methods based on the technique are discussed in detail. Requirements of any laser isotope separation method to be acceptable for the production of heavy water are mentioned and economic viability of this process for heavy water production is examined. Investigations carried out to use this technique for deuterium separation using methanol, formaldehyde, propynal, 2,2,-dichloro-1-1-1,-trifluoroethane (Freon 123), polyvinyl chloride and fluoroform-d are reviewed. (M.G.B.)

  13. Method and apparatus for separating uranium isotopes

    International Nuclear Information System (INIS)

    Bernstein, E.R.

    1977-01-01

    A uranium compound in the solid phase (uranium borohydride four) is subjected to radiation of a first predetermined frequency that excites the uranium-235 isotope-bearing molecules but not the uranium-238 isotope-bearing molecules. The compound is simultaneously subjected to radiation of a second predetermined frequency which causes the excited uranium-235 isotope-bearing molecules to chemically decompose but which does not affect the uranium-238 isotope-bearing molecules. Sufficient heat is then applied to the irradiated compound in the solid phase to vaporize the non-decomposed uranium-238 isotope-bearing molecules but not the decomposed uranium-235 isotope-bearing molecules, thereby physically separating the uranium-235 isotope-bearing molecules from the uranium-238 isotope-bearing molecules. The uranium compound sample in the solid phase is deposited or grown in an elongated tube supported within a dewar vessel having a clear optical path tail section surrounded by a coolant. Two sources of radiation are focused on the uranium compound sample. A heating element is attached to the elongated tube to vaporize the irradiated compound

  14. New processes for uranium isotope separation

    International Nuclear Information System (INIS)

    Vanstrum, P.R.; Levin, S.A.

    1977-01-01

    An overview of the status and prospects for processes other than gaseous diffusion, gas centrifuge, and separation nozzle for uranium isotope separation is presented. The incentive for the development of these processes is the increasing requirements for enriched uranium as fuel for nuclear power plants and the potential for reducing the high costs of enrichment. The latest nuclear power projections are converted to uranium enrichment requirements. The size and timing of the market for new enrichment processes are then determined by subtracting the existing and planned uranium enrichment capacities. It is estimated that to supply this market would require the construction of a large new enrichment plant of 9,000,000 SWU per year capacity, costing about $3 billion each (in 1976 dollars) about every year till the year 2000. A very comprehensive review of uranium isotope separation processes was made in 1971 by the Uranium Isotope Separation Review Ad Hoc Committee of the USAEC. Many of the processes discussed in that review are of little current interest. However, because of new approaches or remaining uncertainties about potential, there is considerable effort or continuing interest in a number of alternative processes. The status and prospects for attaining the requirements for competitive economics are presented for these processes, which include laser, chemical exchange, aerodynamic other than separation nozzle, and plasma processes. A qualitative summary comparison of these processes is made with the gaseous diffusion, gas centrifuge, and separation nozzle processes. In order to complete the overview of new processes for uranium isotope separation, a generic program schedule of typical steps beyond the basic process determination which are required, such as subsystem, module, pilot plant, and finally plant construction, before large-scale production can be attained is presented. Also the present value savings through the year 2000 is shown for various

  15. Novel PEFC Application for Deuterium Isotope Separation

    Directory of Open Access Journals (Sweden)

    Hisayoshi Matsushima

    2017-03-01

    Full Text Available The use of a polymer electrolyte fuel cell (PEFC with a Nafion membrane for isotopic separation of deuterium (D was investigated. Mass analysis at the cathode side indicated that D diffused through the membrane and participated in an isotope exchange reaction. The exchange of D with protium (H in H2O was facilitated by a Pt catalyst. The anodic data showed that the separation efficiency was dependent on the D concentration in the source gas, whereby the water produced during the operation of the PEFC was more enriched in D as the D concentration of the source gas was increased.

  16. Production of exotic beams by separation of online isotope

    International Nuclear Information System (INIS)

    Hosni, Faouzi; Farah, K.

    2013-01-01

    The studies in physics, concerned until now, approximately two thousand five hundred radioactive nuclide. These nuclides with 263 stable nucleus constitute the current nuclear field. This field is far from being complete because there are more than three thousand radioactive isotopes to be discovered. Materials and Methods: To reach these radio-isotopes there are two complementary methods which are the on-line separation (ISOL) and the fragmentation in times of flight. The latter has the advantage to allow the study of the elements of very short period (lower than 10-3 s). It supplies beams having a big dispersal in energy and in angle. In the case of the separation of on-line isotope, a target is run to produce the radioactive atoms. This allows producing beams much more intense than the fragmentation in times of flight. To obtain radioactive beams in the required intensities or for the research or medical applications, it is essential to end in thick targets or the products of reaction can go out as fast as possible. That is to realize targets which can maintain a porous and sluggish structure counterpart in the produced elements. This is one of the main technological challenges to be solved. The works concerning this domain will be presented as well as the got advantage if the nuclear reactions are led by protons reaching 30 MeV of energy. (Author)

  17. Multiple-isotope separation in gas centrifuge

    International Nuclear Information System (INIS)

    Wood, Houston G.; Mason, T.C.; Soubbaramayer

    1996-01-01

    In previous works, the Onsager's pancake equation was used to provide solution to the internal counter-current flow field, which is necessary to calculate solutions to the isotope transport equation. The diffusion coefficient was assumed to be constant which is a good approximation for gases with large molecular weights, and small differences in the molecular weights of the various isotopes. A new optimization strategy was presented for determining the operating parameters of a gas centrifuge to be used for multiple-component isotope separation. Scoop drag, linear wall temperature gradient, the feed rate ant the cut have been chosen as operating parameters for the optimization. The investigation was restricted to a single centrifuge, and the problem of cascading for multiple-isotope separation was not addressed. The model describing the flow and separation phenomena in centrifuge includes a set of equations describing the fluid dynamics of the counter-current flow and the diffusion equations written for each isotope of the mixture. In this paper, an optimization algorithm is described and applied to an example for the re enrichment of spent reactor uranium

  18. Laser assisted jet nozzle isotope separation

    International Nuclear Information System (INIS)

    1981-01-01

    A process for separating fluent particles having different masses comprises the steps of: driving a fluent mixture of such particles around a curved passage toward a septum oriented to divide the mixture thereby accelerating such particles to impart a centrifugal force thereto; inducing type selective heating of a selected particle type in said mixture prior to termination of such acceleration; receiving the fraction of the mixture flowing past an outer surface of said septum in a first output conduit; and receiving the fraction of the mixture flowing past an inner surface of said septum in a second output conduit. The description of the process for isotope separation refers also to the use of infrared laser radiation to produce isotopically selective excitation of the U-235 isotope in UF 6 . (author)

  19. Method for separation and enrichment of isotopes

    International Nuclear Information System (INIS)

    Kakihana, H.; Miyamatsu, T.

    1977-01-01

    Boron or uranium isotopes can be chemically separated and enriched with high speed and with high separating efficiency by using weakly basic anion exchange fibers having a diameter of not more than 100 μ, an aspect ratio of at least 5 and an exchange capacity of at least 2 meq/g-dry fiber, which are packed in a column at a specific volume of 2.0 to 20.0 ml/g-dry fiber

  20. Controlled power supply for isotopes separator

    International Nuclear Information System (INIS)

    Lavaitte, A.; Pottier, J.

    1953-01-01

    This equipment is destined to equip the separator of isotopes who is the subject of the CEA report n 138. It includes: - a controlled power supply in voltage. - a controlled power supply in current. The spectra of fluctuations of these assembly is different in the two cases. (authors) [fr

  1. Environmental Development Plan for advanced isotope separation

    International Nuclear Information System (INIS)

    1979-05-01

    This EDP identifies the planning and management requirements and schedules needed to evaluate and assess the environmental, health, and safety aspects of the Advanced Isotope Separation (AIS) program. Current AIS processes include the molecular and atomic vapor laser processes and the plasma process. This document covers the technology program, environmental concerns and requirements, and environmental strategy

  2. Atomic-vapor-laser isotope separation

    International Nuclear Information System (INIS)

    Davis, J.I.

    1982-10-01

    This paper gives a brief history of the scientific considerations leading to the development of laser isotope separation (LIS) processes. The close relationship of LIS to the broader field of laser-induced chemical processes is evaluated in terms of physical criteria to achieve an efficient production process. Atomic-vapor LIS processes under development at Livermore are reviwed. 8 figures

  3. INS gas-filled recoil isotope separator

    International Nuclear Information System (INIS)

    Miyatake, M.; Nomura, T.; Kawakami, H.

    1986-09-01

    The characteristics and performance of a small sized gas-filled recoil isotope separator recently made at INS are described. The total efficiency and the ΔBρ/Bρ values have been measured using low velocity 16 O, 40 Ar and 68 As ions and found to be 10 and 5 %, respectively. The Z-dependence of the mean charge is discussed. (author)

  4. Separation of compounds differing in isotopic composition

    International Nuclear Information System (INIS)

    Sievers, R.E.; Brooks, J.J.

    1976-01-01

    Compounds differing in isotopic composition are separated by introducing a mixture of the compounds into a chromatographic column containing a lanthanide chelate as a stationary phase and eluting from the column a fraction which is at least enriched with one of the compounds of the mixture. 17 claims, no drawings

  5. Separation of compounds differing in isotopic composition

    International Nuclear Information System (INIS)

    Sievers, R.E.; Brooks, J.J.

    1975-01-01

    Compounds differing in isotopic composition are separated by introducing a mixture of the compounds into a chromatographic column containing a lanthanide chelate as a stationary phase and eluting from the column a fraction that is at least enriched with one of the compounds of the mixture. (U.S.)

  6. Molecular laser isotope separation programme at BARC

    International Nuclear Information System (INIS)

    Sarkar, Sisir K.; Parthasarathy, Venkatachari

    2007-09-01

    Little over thirty years ago, BARC ventured into a new frontier of scientific research: Molecular Laser Isotope Separation (MLIS) programme based on the interaction of lasers with molecules. The initial project was a scheme to produce enriched uranium. The idea was to use the intense, monochromatic light of lasers to break the chemical bonds of only those molecules containing the fissionable isotope uranium-235. At present the programme is evolving around separation of low and middle mass isotopes, namely sulphur 34/33/32, oxygen 17/18, carbon 13/12, hydrogen T/D/H to be followed by an advanced engineering programme designed to lead to a demonstration plant. The latest results have come very close to the design parameters specified for a full-scale separation of carbon isotopes. All these expertise provide an infra structure for future front line R and D activities in the general area of Laser Photochemical Technology which would include i) LIS of other useful elements ii) Material processing and iii) Fuel reprocessing/ waste management (author)

  7. Separation of Hydrogen Isotopes by Palladium Alloy Membranes Separator

    International Nuclear Information System (INIS)

    Jiangfeng, S.; Deli, L.; Yifu, X.; Congxian, L.; Zhiyong, H.

    2007-01-01

    Full text of publication follows: Separation of hydrogen isotope with palladium alloy membranes is one of the promising methods for hydrogen isotope separation. It has several advantages, such as high separation efficiency, smaller tritium inventory, simple separation device, ect. Limited by the manufacture of membrane and cost of gas transportation pump, this method is still at the stage of conceptual study. The relationship between separation factors and temperatures, feed gas components, split ratios have not been researched in detail, and the calculated results of cascade separation have not been validated with experimental data. In this thesis, a palladium alloy membrane separator was designed to further study its separation performance between H 2 and D 2 . The separation factor of the single stage was affected by the temperature, the feed gas component, the split ratio and the gas flow rate, etc. The experimental results showed that the H 2 -D 2 separation factor decreased with the increasing of temperature. On the temperature from 573 K to 773 K, when the feed rate was 5 L/min, the separation factor of 66.2%H 2 - 33.8%D 2 decreased from 2.09 to 1.85 when the split ratio was 0.1 and from 1.74 to 1.52 when the split ratio was 0.2.The separation factor also decreased with the increasing of split ratio. At 573 K and the feed rate of 5 L/min, the separation factor of 15.0%H 2 and 85.0%D 2 decreased from 2.43 to 1.35 with the increasing of split ratio from 0.050 to 0.534,and for 66.2%H 2 -33.8%D 2 , the separation factor decreased from 2.87 to 1.30 with the increasing of split ratio from 0.050 to 0.688. When the separation factor was the biggest, the flow rate of feed gas was in a perfect value. To gain a best separation performance, perfect flow rate, lower temperature and reflux ratio should be chosen. (authors)

  8. Separation of uranium isotopes by gas centrifugation

    International Nuclear Information System (INIS)

    Jordan, I.

    1980-05-01

    The uranium isotope enrichment is studied by means of the countercurrent gas centrifuge driven by thermal convection. A description is given of (a) the transfer and purification of the uranium hexafluoride used as process gas in the present investigation; (b) the countercurrent centrifuge ZG3; (c) the system designed for the introduction and extraction of the process gas from the centrifuge; (d) the measurement of the process gas flow rate through the centrifuge; (e) the determination of the uranium isotopic abundance by mass spectrometry; (f) the operation and mechanical behavior of the centrifuge and (g) the isotope separation experiments, performed, respectively, at total reflux and with production of enriched material. The results from the separation experiments at total reflux are discussed in terms of the enrichment factor variation with the magnitude and flow profile of the countercurrent given by the temperature difference between the rotor covers. As far as the separation experiments with production are concerned, the discussion of their results is presented through the variation of the enrichment factor as a function of the flow rate, the observed asymmetry of the process and the calculated separative power of the centrifuge. (Author) [pt

  9. Separation of isotopes by cyclical processes

    International Nuclear Information System (INIS)

    Hamrin, C.E. Jr.; Weaver, K.

    1976-01-01

    Various isotopes of hydrogen are separated by a cyclic sorption process in which a gas stream containing the isotopes is periodically passed through a high pressure column containing a palladium sorbent. A portion of the product from the high pressure column is passed through a second column at lower pressure to act as a purge. Before the sorbent in the high pressure column becomes saturated, the sequence is reversed with the stream flowing through the former low-pressure column now at high pressure, and a portion of the product purging the former high pressure column now at low pressure. The sequence is continued in cyclic manner with the product being enriched in a particular isotope

  10. Neutron separation energies of Zr isotopes

    International Nuclear Information System (INIS)

    Gomes, L.C.; Dietzsch, O.

    1976-01-01

    Q values are reported for (d,t) reactions on all the stable isotopes of zirconium. The neutron separation energies of 94 Zr and 96 Zr differ greatly (by 27.5 and 22.1 keV, respectively) from the values in the 1971 Atomic Mass Evaluation. These results combined with those from other authors seem to indicate that the 1971 values for the masses of 93 Zr and 95 Zr are in error. (orig.) [de

  11. Process and component for isotope separation

    International Nuclear Information System (INIS)

    Girodin, M.G.H.

    1974-01-01

    The description is given of a component for isotope separation by static centrifugation, the characteristic of which is that the gas, of single chemical composition, in other words without a diluting gas mixture, passes into a sonic collar then into a symmetrical supersonic diffuser where it acquires a uniform and rectilinear velocity above or very much above the speed of sound before going into its curved trajectory [fr

  12. Isotopic separation by centrifugation. Rotating plasma

    International Nuclear Information System (INIS)

    Perello, M.; Vigon, M. A.

    1972-01-01

    The motion of a gas simultaneously submitted to an electric discharge and magnetic field has been studied in order to analyze the possibility of producing isotopes separation by rotation of a plasma. Some experimental results obtained under different discharge conditions are also given. Differences of pressure up to 15 mm oil between both electrodes has been attained. No definite conclusion on separation factors could be reached because of the low reproducibility of results, probably due to the short duration of the discharge with a new chamber designed to support stronger thermal shocks more reliable data can be expected. (Author) 16 refs

  13. Isotope separation in crossed-jet systems

    Energy Technology Data Exchange (ETDEWEB)

    Gallagher, R.J.; Anderson, J.B.

    1978-11-01

    The separation of isotopes in crossed-jet systems was investigated with Monte Carlo calculations of the separation effects for jets of Ne/Ar and /sup 235/UF/sub 6///sup 238/UF/sub 6/ mixtures entering a hydrogen stream. For the ideal condition of uniform stream velocities at zero temperature, the separation factor ..cap alpha.. was found to be 16.0 for Ne/Ar and 1.17 for /sup 235/UF/sub 6///sup 238/UF/sub 6/. For less ideal but more practical conditions, Monte Carlo calculations of the complete crossed-jet systems gave separation factors as high as 3.3 for Ne/Ar and ..cap alpha.. = 1.046 - 1.078 for /sup 235/UF/sub 6///sup 238/UF/sub 6/.

  14. Application of gas chromatography in hydrogen isotope separation

    International Nuclear Information System (INIS)

    Ye Xiaoqiu; Sang Ge; Peng Lixia; Xue Yan; Cao Wei

    2008-01-01

    The principle of gas chromatographic separation of hydrogen isotopes was briefly introduced. The main technology and their development of separating hydrogen isotopes, including elution chromatography, hydrogen-displacement chromatography, self-displacement chromatography and frontal chromatography were discussed in detail. The prospect of hydrogen isotope separation by gas chromatography was presented. (authors)

  15. Isotope separation in plasma by ion-cyclotron resonance method

    International Nuclear Information System (INIS)

    Dubinov, A.E.; Kornilova, I.Yu.; Selemir, V.D.

    2001-01-01

    Contemporary state of investigation on isotope separation in plasma using selective ion-cyclotron resonance (ICR) heating is considered. The main attention is paid to necessary conditions of heating selectivity, plasma creation methods in isotope ICR-separation facilities, selection of antenna systems for heating, and principles of more-heated component selection. Experimental results obtained at different isotope mixtures separation are presented [ru

  16. Memories of Professor Sugimoto and isotope separator

    International Nuclear Information System (INIS)

    Tanaka, Kazuhiro

    2013-01-01

    Usual magnetic isotope-separators select the particles with the same Z/A value which may include different nuclides. Identification of the isotope with the same Z/A value but different Z or A value is an universal requirement for nuclear physics experiments. If one knows, together with the A/Z value, the dE/dx or the range of the isotope in some energy absorber, which are the function of Z 2 /A, its nuclide can be specified. This idea can be realized by arranging proper energy-absorber at the focal point of magnetic analyzer. The author proposes another novel method in which two dipole-magnets are excited with some difference, and an energy absorber corresponding to that energy difference is situated between two magnets. It can also be devised so that the dispersion at the final focal-point depends only on the emission angle of the isotope at production. Professor Sugimoto recognized the significance of this scheme and proposed to employ it in the experiment at BEVATRON. The unbalanced two dipole-magnets method is employed at RIKEN and RCNP, Osaka University. The author's creative idea originated in Sugimoto Laboratory at Osaka University. (author)

  17. The isotope separation by ion exchange chromatography. Application to the lithium isotopes separation

    International Nuclear Information System (INIS)

    Albert, M.G.; Barre, Y.; Neige, R.

    1993-01-01

    In this work is described the used study step to demonstrate the industrial feasibility of a lithium isotopes separation process by ion exchange chromatography. After having recalled how is carried out the exchange reaction between the lithium isotopes bound on the cations exchanger resin and those which are in solution and gave the ion exchange chromatography principle, the authors establish a model which takes into account the cascade theory already used for enriched uranium production. The size parameters of this model are: the isotopic separation factor (which depends for lithium of the ligands nature and of the coordination factor), the isotopic exchange kinetics and the mass flow (which depends of the temperature, the lithium concentration, the resins diameter and the front advance). The way they have to be optimized and the implementation of the industrial process are given. (O.M.)

  18. Isotopic separation in a rotating neon plasma

    International Nuclear Information System (INIS)

    Cairns, J.B.S.

    1976-01-01

    The background to the use of rotating plasma as element and isotope separators is briefly reviewed. The principles of the process are outlined. The rotation in a plasma centrifuge is produced by passing a radial current across an axial magnetic field. The different mass spheres, if under the influence of azimuthal forces, may be separated by crossing the field. Details are given of the Vortex II experiment in which 22 Ne is separated from neon in a fully ionized rotating plasma. It was demonstrated that 22 Ne enrichments of approximately 15% could be achieved with the possibility of higher values when the design and operation of the plasma centrifuge have been optimised. (U.K.)

  19. Electrical circuits of an electromagnetic isotope separator

    International Nuclear Information System (INIS)

    Neyron, A.

    1959-01-01

    After an outline of the general principles governing the operation of an electromagnetic isotope separator, the electrical characteristics necessary to this operation are given. First the electrical characteristics of the ion source are briefly presented. The author then gives a detailed account of the construction of the H.T. acceleration supply of which the maxima characteristics are 80 kV and 150 mA with stabilisation of the order of 4.10 -4 . Reprint of a paper published in 'Industries Atomiques' - n. 3-4, 1959

  20. Operation manual for the INEL on-line mass-separator facility

    International Nuclear Information System (INIS)

    Anderl, R.A.

    1984-06-01

    This report is an operation manual for an on-line mass-separator facility which is located in Building 661 at the Test Reactor Area of the Idaho National Engineering Laboratory. The facility provides mass-separated sources of short-lived fission-product radionuclides whose decay properties can be studied using a variety of nuclear spectroscopic techniques. This facility is unique in that it utilizes the gas-jet technique to transport fission products from a 252 Cf source located in a hot cell to the ion source of the mass separator. This document includes the following: (a) a detailed description of the facility, (b) identification of equipment hazards and safety controls, (c) detailed operating procedures for startup, continuous operation and shutdown, (d) operating procedures for the californium hot cell, and (e) an operator's manual for the automated moving tape collector/data acquisition system. 7 references, 16 figures, 8 tables

  1. Optimization of the isotope separation in columns

    International Nuclear Information System (INIS)

    Kaminskij, V.A.; Vetsko, V.M.; Tevzadze, G.A.; Devdariani, O.A.; Sulaberidze, G.A.

    1982-01-01

    The general method for the multi-parameter optimization of cascade plants of packed columns is proposed. As an optimization effectiveness function a netcost of the isotopic product is selected. The net cost is comprehensively characterizing the sum total of capital costs for manufacturing the products as well as determining the choice of the most effective directions for capital investments and rational limits of improvement of the products quality. The method is based on main representations of the cascade theory, such as the ideal flow profile and form efficiency as well as mathematical model of the packed column specifying the bonds between its geometric and operating parameters. As a result, the isotopic products cost function could be bound with such parameters as the equilibrium stage height, ultimate packing capacity, its element dimensions, column diameter. It is concluded that the suggested approach to the optimization of isotope separation processes is rather a general one. It permits to solve a number of special problems, such as estimation of advisability of using heat-pump circuits and determining the rational automation level. Besides, by means of the method suggested one can optimize the process conditions with regard to temperature and pressure

  2. Isotope separation using vibrationally excited molecules

    International Nuclear Information System (INIS)

    Woodroffe, J.A.; Keck, J.C.

    1979-01-01

    Vibrational excitation of molecules having components of a selected isotope type is used to produce a conversion from vibrational to translational excitation of the molecules by collision with the molecules of a heavy carrier gas. The resulting difference in translaton between the molecules of the selected isotope type and all other molecules of the same compound permits their separate collection. When applied to uranium enrichment, a subsonic cryogenic flow of molecules of uranium hexafluoride in combination with an argon carrier gas is directed through a cooled chamber that is illuminated by laser radiaton tuned to vibrationally excite the uranium hexafluoride molecules of a specific uranium isotope. The excited molecules collide with carrier gas molecules, causing a conversion of the excitation energy into a translation of the excited molecule, which results in a higher thermal energy or diffusivity than that of the other uranium hexafluoride molecules. The flowing molecules including the excited molecules directly enter a set of cryogenically cooled channels. The higher thermal velocity of the excited molecules increases the probability of their striking a collector surface. The molecules which strike this surface immediately condense. After a predetermined thickness of molecules is collected on the surface, the flow of uranium hexafluoride is interrupted and the chamber heated to the point of vaporization of the collected hexafluoride, permitting its removal. (LL)

  3. Innovative lasers for uranium isotope separation

    International Nuclear Information System (INIS)

    Brake, M.L.; Gilgenbach, R.M.

    1993-07-01

    Copper vapor laser have important applications to uranium atomic vapor laser isotope separation (AVLIS). We have investigated two innovative methods of exciting/pumping copper vapor lasers which have the potential to improve the efficiency and scaling of large laser systems used in uranium isotope separation. Experimental research has focused on the laser discharge kinetics of (1) microwave, and (2) electron beam excitation/pumping of large-volume copper vapor lasers. Microwave resonant cavity produced copper vapor plasmas at 2.45 GHz, have been investigated in three separate experimental configurations. The first examined the application of CW (0-500W) power and was found to be an excellent method for producing an atomic copper vapor from copper chloride. The second used a pulsed (5kW, 0.5--5 kHz) signal superimposed on the CW signal to attempt to produce vaporization, dissociation and excitation to the laser states. Enhanced emission of the optical radiation was observed but power densities were found to be too low to achieve lasing. In a third experiment we attempted to increase the applied power by using a high power magnetron to produce 100 kW of pulsed power. Unfortunately, difficulties with the magnetron power supply were encountered leaving inconclusive results. Detailed modeling of the electromagnetics of the system were found to match the diagnostics results well. An electron beam pumped copper vapor system (350 kV, 1.0 kA, 300 ns) was investigated in three separate copper chloride heating systems, external chamber, externally heated chamber and an internally heated chamber. Since atomic copper spectral lines were not observed, it is assumed that a single pulse accelerator is not capable of both dissociating the copper chloride and exciting atomic copper and a repetitively pulsed electron beam generator is needed

  4. Hydrogen isotope separation for fusion power applications

    Energy Technology Data Exchange (ETDEWEB)

    Smith, R., E-mail: robert.smith@ccfe.ac.uk [EURATOM/CCFE Fusion Association, Culham Science Centre, Abingdon OX14 3DB (United Kingdom); JET-EFDA, Culham Science Centre, Abingdon OX14 3DB (United Kingdom); Whittaker, D.A.J.; Butler, B.; Hollingsworth, A.; Lawless, R.E.; Lefebvre, X.; Medley, S.A.; Parracho, A.I.; Wakeling, B. [EURATOM/CCFE Fusion Association, Culham Science Centre, Abingdon OX14 3DB (United Kingdom); JET-EFDA, Culham Science Centre, Abingdon OX14 3DB (United Kingdom)

    2015-10-05

    Highlights: • Summary of the tritium plant, the Active Gas Handling System (AGHS), at JET. • Review of the Water Detritiation System (WDS) under construction. • Design of the new Material Detritiation Facility (MDF). • Review of problems in fusion related to metal/hydrogen system. - Abstract: The invited talk given at MH2014 in Salford ranged over many issues associated with hydrogen isotope separation, fusion machines and the hydrogen/metal systems found in the Joint European Torus (JET) machine located near Oxford. As this sort of talk does not lend itself well to a paper below I have attempted to highlight some of the more pertinent information. After a description of the Active Gas Handling System (AGHS) a brief summary of isotope separation systems is described followed by descriptions of three major projects currently being undertaken by the Tritium Engineering and Science Group (TESG), the upgrade to the Analytical Systems (AN-GC) at the AGH, the construction of a Water Detritiation System (WDS) and a Material Detritiation Facility (MDF). Finally, a review of some of the challenges facing fusion with respect to metal/hydrogen systems is presented.

  5. Application of ion exchange to isotope separation. 2. Isotope separation of uranium

    Energy Technology Data Exchange (ETDEWEB)

    Okamoto, Makoto; Fujii, Yasuhiko; Aida, Masao; Nomura, Masao; Aoyama, Taku

    1985-10-01

    Research work on the uranium isotope separation by ion exchange chromatography done by the ahthors was reviewed and summarized in the present paper. Specifically described are the determination of separation coefficients of uranium isotopes in various chemical systems involving uranium ions and complexes. The chemical systems are classifield into three main categories; (1) uranyl, U (VI), complex formation system, (2) uranous, U (IV), complex formation system and (3) U (IV) - U (VI) redox system. The redox system showed the largest separation coefficient of approx. 7 x 10/sup -4/, while the uranyl and uranous complex systems showed the separation coefficients of -- 2 x 10/sup -4/ and approx. 6 x 10/sup -5/, respectively.

  6. The isotope separation by ion exchange chromatography. Application to the lithium isotopes separation; La separation isotopique par chromatographie ionique

    Energy Technology Data Exchange (ETDEWEB)

    Albert, M G; Barre, Y; Neige, R

    1994-12-31

    In this work is described the used study step to demonstrate the industrial feasibility of a lithium isotopes separation process by ion exchange chromatography. After having recalled how is carried out the exchange reaction between the lithium isotopes bound on the cations exchanger resin and those which are in solution and gave the ion exchange chromatography principle, the authors establish a model which takes into account the cascade theory already used for enriched uranium production. The size parameters of this model are: the isotopic separation factor (which depends for lithium of the ligands nature and of the coordination factor), the isotopic exchange kinetics and the mass flow (which depends of the temperature, the lithium concentration, the resins diameter and the front advance). The way they have to be optimized and the implementation of the industrial process are given. (O.M.). 5 refs.

  7. Study of the isotopic contamination with the Grenoble isotope separator

    International Nuclear Information System (INIS)

    Boge, Marc

    1970-01-01

    To know the limits of enrichment of the Grenoble electromagnetic isotope separator, we have studied the scattering of ions on the residual gas, and the chromatism. With Neodymium (Nd + ≅ 500 μA, NdO + ≅ 120 μA, Nd 2+ ≅ 70 μA) the second magnet has been used to analyse the ions which passed through the first stage slit. Therefore, we have measured the scattering with and without charge exchange of Nd + and the dissociation of NdO + . The chromatism has been studied by means of an electrostatic analyser, as a third stage. The limits of enrichment are obtained for Argon, Uranium and Neodymium. (author) [fr

  8. Some characteristics of isotopic separation laser systems

    International Nuclear Information System (INIS)

    Pochon, E.

    1988-01-01

    The principle of Laser Isotope Separation (LIS) is simple and based on either selective electronic photoexcitation and photoionization of atomic vapor, or selective vibrational photoexcitation and photodissociation of molecules in the gas phase. These processes, respectively called SILVA (AVLIS) and SILMO (MLIS) in France, both use specific laser systems with wavelengths spanning from infrared to ultraviolet. This article describes briefly some of the characteristics of a SILVA laser system. Following a three-step process, a SILVA laser system is based on dye copper vapor lasers. The pulse dye lasers provide the tunable laser light and are optically pumped by copper vapor laser operating at high repetition rates. In order to meet plant laser system requirements, the main improvements under way relate to copper vapor laser devices the power capability, efficiency, reliability and lifetime of which have to be increased. 1 fig

  9. Multicomponent isotopic separation and recirculation analysis

    International Nuclear Information System (INIS)

    Misra, B.; Maroni, V.A.

    1976-01-01

    A digital computer program for design of multicomponent distillation columns has been developed based on an exact method of solution of the governing equations. Although this computer program was developed for enrichment of the spent fuels from presently conceived tokamak-type fusion power reactors by cryogenic distillation, the program can be used for the design of any multicomponent distillation column, provided, of course, the necessary thermodynamic and phase equilibrium data are available. To prove the versatility of the computer program, parametric investigations to study the effect of design and operating variables on the composition of the product streams was carried out for the case of separating hydrogen isotopes. The computer program is very efficient; hence, a number of parametric investigations can be carried out with limited resources. The program does, however, require a fairly large computer storage space

  10. Cascade theory in isotopic separation processes

    International Nuclear Information System (INIS)

    Agostini, J.P.

    1994-06-01

    Three main areas are developed within the scope of this work: - the first one is devoted to fundamentals: separative power, value function, ideal cascade and square cascade. Applications to two main cases are carried out, namely: Study of binary isotopic mix, Study of processes with a small enrichment coefficient. - The second one is devoted to cascade coupling -high-flux coupling (more widely used and better known) as well as low-flux coupling are presented and compared to one another. - The third one is an outlook on problems linked to cascade transients. Those problem are somewhat intricate and their interest lies mainly into two areas: economics where the start-up time may have a large influence on the interests paid during the construction and start-up period, military productions where the start-up time has a direct bearing on the production schedule. (author). 50 figs. 3 annexes. 12 refs. 6 tabs

  11. Thermal diffusion and separation of isotopes

    International Nuclear Information System (INIS)

    Fournier, Andre

    1944-01-01

    After a review of the various processes used to separate isotopes or at least to obtain mixes with a composition different from the natural proportion, this research addresses the use of thermal diffusion. The author reports a theoretical study of gas thermal diffusion and of the Clusius-Dickel method. In the second part, he reports the enrichment of methane with carbon-13, and of ammoniac with nitrogen-15. The next part reports the experimental study of thermal diffusion of liquids and solutions, and the enrichment of carbon tetra-chloride with chlorine-37. The author then proposes an overview of theories of thermal diffusion in liquid phase (hydrodynamic theory, kinetic theory, theory of caged molecules)

  12. Method of deuterium isotope separation and enrichment

    International Nuclear Information System (INIS)

    Benson, S.W.

    1980-01-01

    A method of deuterium isotope separation and enrichment using infrared laser technology in combination with chemical processes for treating and recycling the unreacted and deuterium-depleted starting materials is described. Organic molecules of the formula RX (where R is an ethyl, isopropyl, t-butyl, or cyclopentenyl group and X is F, Cl, Br or OH) containing a normal abundance of hydrogen and deuterium are exposed to intense laser infrared radiation. An olefin containing deuterium (olefin D) will be formed, along with HX. The enriched olefin D can be stripped from the depleted stream of RX and HX, and can be burned to form enriched water or pyrolyzed to produce hydrogen gas with elevated deuterium content. The depleted RX is decomposed to olefins and RX, catalytically exchanged with normal water to restore the deuterium content to natural levels, and recombined to form RX which can be recycled. (LL)

  13. Mathematical Modeling of Nonstationary Separation Processes in Gas Centrifuge Cascade for Separation of Multicomponent Isotope Mixtures

    Directory of Open Access Journals (Sweden)

    Orlov Alexey

    2016-01-01

    Full Text Available This article presents results of development of the mathematical model of nonstationary separation processes occurring in gas centrifuge cascades for separation of multicomponent isotope mixtures. This model was used for the calculation parameters of gas centrifuge cascade for separation of germanium isotopes. Comparison of obtained values with results of other authors revealed that developed mathematical model is adequate to describe nonstationary separation processes in gas centrifuge cascades for separation of multicomponent isotope mixtures.

  14. Thermally-controlled centrifuge for isotopic separation

    International Nuclear Information System (INIS)

    Cenedese, A.; Cunsolo, D.

    1976-01-01

    Among the various methods proposed to obtain lighter component enrichment in the isotopic separation of uranium, ultracentrifugation is becoming more and more interesting today, as this process becomes a useful alternate method to gaseous diffusion. The ultracentrifuge main gas-dynamic features are investigated in the present study. In particular, the field inside the centrifuge has been subdivided into three axial zones: an internal central zone, characterized by an essentially axial flow; two external zones, near the two caps of the centrifuge; two intermediate zones, of a length of the order of the radius. For the analytical solution the linearized Navier-Stokes equations have been considered. The central zone flow is solved by separating the independent variables; the corresponding eigenvalue problem has been solved numerically. A series of eigensolutions which satisfy boundary conditions at the walls of the cylinder has been calculated. An integral method for the superimposition of the above mentioned eigensolutions is proposed in order to satisfy the conditions at the tops for thermally-controlled centrifuges. (author)

  15. Atomic vapor laser isotope separation in France

    International Nuclear Information System (INIS)

    Camarcat, N.; Lafon, A.; Perves, J.P.; Rosengard, A.

    1992-01-01

    The main effort in the field of Isotopic Separation Research and Development in France is devoted since 1985 to the 'SILVA' process. A structured organization has been set up, including the following elements: Specific Research and Development for all the functions and components of the process: this work is supported by numerous benches located in Saclay and Pierrelatte. Each bench is mainly devoted to one process function; regarding process and operating performances are optimized. Integrated Experiences in a Pilot facility. Qualified components are integrated in a pilot facility located in Saclay, the capacity of which is steadily increased. At each stage, complete separative experiments demonstrate the improvements attained. Focused Basic Research for each field, often linked with various and relatively original phenomenas. Models have been built up, supported by specific experiments and values attained for intrinsical parameters. An aggregated process performance computing code integrates all the models, possibly under simplified form. Technical, operating and economical data are gradually added. A general assessment will take place in the middle of the nineties with several technical demonstrations and a complete evaluation of the French AVLIS process

  16. Isotope separation in a rotational plasma

    International Nuclear Information System (INIS)

    Tomimura, A.; Nicoli, C.

    1985-03-01

    The model of a steady cascade in a plasma confined between two cylindrical electrodes and immersed in a homogenous and axial magnetic field is constructed in order to study the separation properties of the elements that make up its mono-ionised ionic species. Rotation is imposed over a column of plasma through the interaction J x B and sufficiently balanced by viscous friction. In the radial direction the pinch effect, due to the radial component of the J x B interaction, counterbalances the pressure gradient which is bigger than the centrifugal force. A uranium gas with its two principal isotopes (U 235 and U 238 ) constitutes an ionic species of plasma. The numerical scheme designed to resolve the system of equations containing variables of density, temperature and velocity as a function of the radius promises solutions that satisfy null contour conditions for velocity in the two contours (external and internal electrodes). Maximum typical values of velocity and separation factor at temperatures and densities (in the internal electrode) of the order of 60 000 K and 5 x 10 15 cm -3 are, for example, 11.8 km/s and 1.4 respectively. Bigger values can be obtained, depending on the values of the free parameters in the internal electrode

  17. Advances in the helium-jet coupled on-line mass separator RAMA

    International Nuclear Information System (INIS)

    Moltz, D.M.; Aysto, J.; Cable, M.D.; Parry, R.F.; Haustein, P.E.; Wouters, J.M.; Cerny, J.

    1980-01-01

    General improvements to the on-line mass separator RAMA (Recoil Atom Mass Analyzer) have yielded a greater reliability and efficiency for some elements. A new utilitarian helium-jet chamber has been installed to facilitate quick target and degrader foil changes in addition to a new ion source holder. A higher efficiency hollow-cathode, cathode-extraction ion source, for lower melting point elements ( 0 C) has also been designed. Tests with the beta-delayed proton emitter 37 Ca showed a factor of five increase in yield over the old hollow-cathode, anode-extraction source. A differentially-pumped-tape drive system compatible with both γ-γ and β-γ experiments has been incorporated into the general detection system. All major operating parameters will soon be monitored by a complete stand-alone microprocessor system which will eventually be upgraded to a closed-loop control system

  18. The isotopic contamination in electromagnetic isotope separators; La contagion isotopique dans les separateurs electromagnetiques d'isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Cassignol, Ch [Commissariat a l' Energie Atomique, Saclay (France).Centre d' Etudes Nucleaires

    1959-07-01

    In the early years of isotope separation, and in particular electromagnetic isotope separation, needs for rapid results have conducted to empiric research. This paper describes fundamental research on the electromagnetic isotope separation to a better understanding of isotope separators as well as improving the performances. Focus has been made on the study of the principle of isotope contamination and the remedial action on the separator to improve the isotope separation ratio. In a first part, the author come back to the functioning of an electromagnetic separator and generalities on isotope contamination. Secondly, it describes the two stages separation method with two dispersive apparatus, an electromagnetic separation stage followed by an electrostatic separation stage, both separated by a diaphragm. The specifications of the electrostatic stage are given and its different settings and their consequences on isotope separation are investigated. In a third part, mechanisms and contamination factors in the isotope separation are discussed: natural isotope contamination, contamination by rebounding on the collector, contamination because of a low resolution, contamination by chromatism and diffusion effect, breakdown of condenser voltage. Analysis of experimental results shows the diffusion as the most important contamination factor in electromagnetic isotope separation. As contamination factors are dependent on geometric parameters, sector angle, radius of curvature in the magnetic field and clearance height are discussed in a fourth part. The better understanding of the mechanism of the different contamination factors and the study of influential parameters as pressure and geometric parameters lead to define a global scheme of isotope contamination and determinate optima separator design and experimental parameters. Finally, the global scheme of isotope contamination and hypothesis on optima specifications and experimental parameters has been checked during a

  19. The isotopic contamination in electromagnetic isotope separators; La contagion isotopique dans les separateurs electromagnetiques d'isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Cassignol, Ch. [Commissariat a l' Energie Atomique, Saclay (France).Centre d' Etudes Nucleaires

    1959-07-01

    In the early years of isotope separation, and in particular electromagnetic isotope separation, needs for rapid results have conducted to empiric research. This paper describes fundamental research on the electromagnetic isotope separation to a better understanding of isotope separators as well as improving the performances. Focus has been made on the study of the principle of isotope contamination and the remedial action on the separator to improve the isotope separation ratio. In a first part, the author come back to the functioning of an electromagnetic separator and generalities on isotope contamination. Secondly, it describes the two stages separation method with two dispersive apparatus, an electromagnetic separation stage followed by an electrostatic separation stage, both separated by a diaphragm. The specifications of the electrostatic stage are given and its different settings and their consequences on isotope separation are investigated. In a third part, mechanisms and contamination factors in the isotope separation are discussed: natural isotope contamination, contamination by rebounding on the collector, contamination because of a low resolution, contamination by chromatism and diffusion effect, breakdown of condenser voltage. Analysis of experimental results shows the diffusion as the most important contamination factor in electromagnetic isotope separation. As contamination factors are dependent on geometric parameters, sector angle, radius of curvature in the magnetic field and clearance height are discussed in a fourth part. The better understanding of the mechanism of the different contamination factors and the study of influential parameters as pressure and geometric parameters lead to define a global scheme of isotope contamination and determinate optima separator design and experimental parameters. Finally, the global scheme of isotope contamination and hypothesis on optima specifications and experimental parameters has been checked during a

  20. On the problems of separation work unit for the laser isotope separation

    International Nuclear Information System (INIS)

    Wang, Lijun

    2008-01-01

    The concept of separation power or separation work, which is widely used in Uranium isotope separation industry is introduced historically for the weak separating machine and so-called 'ideal cascade'. Therefore, when this concept is applied to a laser isotope separation facility, which is deeply different from a cascade in structure and in mechanism of separation, some confusions may occur. By comparison the costs of SWU of laser isotope separation facility and an ideal cascade we come to a conclusion: the concept of separation work is not applicable for laser isotope separation. In order to compare the economics of laser isotope separation technique with diffusion or centrifugation techniques an equivalent cost of SWU is suggested in this paper. (author)

  1. Laser pumped lasers for isotope separation

    International Nuclear Information System (INIS)

    Fry, S.M.

    1976-01-01

    A study of the isotope separation laser requirements reveals that high pressure polyatomic molecular gas laser pumped lasers can attain the necessary characteristics including tunability, energy output, pulse width, and repetition rate. The results of a search, made for molecules meeting the appropriate requirements for one of several pump schemes utilizing a CO 2 laser and with output in the 12 μm or 16μm wavelength range, are presented. Several methods of pumping are reviewed and two novel pump schemes are presented. A laser pumped laser device design is given, and operation of this device and associated diagnostic equipment is confirmed by repeating experiments in OCS and NH 3 . The results of OCS laser experiments show that an improvement in pump rate and output per unit length is obtained with the device, using a wedged transverse pumping scheme. A new multi-line laser system in NH 3 pumped by a TEA CO 2 laser is reported. More than forty transitions spanning the wavelength range of 9.2 to 13.8 μm are observed and identified. A strong output at 12.08 μm is one of the closest lines yet found to the required laser isotope separation wavelength. Far infrared emission near 65 μm is observed and is responsible for populating levels which lase in pure ammonia near 12.3 μm. Buffer gas (e.g., N 2 or He) pressures of approximately 40--800 torr cause energy transfer by collision-induced rotationaltransitions from the pumped antisymmetric to the lasing symmetric levels in the nu 2 = 1 band of ammonia. Most of the observed lines are aP(J,K) transitions which originate from the nu 2 /sup s/ band. Measurements of the pressure dependence of the laser output shows that some lines lase at pressures greater than one atmosphere. Transient behavior of the 12.08 μm line is calculated from a simplified analytic model and these calculations are compared to the experimental results

  2. Separation of the mercury isotopes by the indirect photochemical method

    International Nuclear Information System (INIS)

    Botter nee Bergheaud, F.; Scaringella nee Desnoyer, M.; Wacongne, M.

    1976-01-01

    A method of photochemical separation of the mercury isotopes by the so-called indirect route in which a gas stream of oxygen and butadiene containing a mixture of mercury isotopes is passed through one or a number of vessels placed in series. The gas stream is irradiated by a lamp containing mercury which is depleted in one or a number of the isotopes and said isotopes are recovered in a trap placed downstream of the vessel or vessels

  3. Separation of hydrogen isotopes via single column pressure swing adsorption

    International Nuclear Information System (INIS)

    Wong, Y.W.; Hill, F.B.

    1981-01-01

    Separation of hydrogen isotopes based on kinetic isotope effects was studied. The mixture separated was hydrogen containing a trace of tritium as HT and the hydride was vanadium monohydride. The separation was achieved using the single-column pressure swing process. Stage separation factors are larger and product cuts smaller than for a two-column pressure swing process operated in the same monohydride phase

  4. Procedure and device for separating isotopes of high mass

    International Nuclear Information System (INIS)

    Eerkens, J.W.

    1977-01-01

    The invention refers to isotope separation and to selectively photon-induced energy transfer from an isotope molecule containing the isotope to be separated as well as to a chemical reaction with a reactive agent in order to produce a chemical compound containing atoms of the desired isotope. For example, in the most preferable form of the invention, gaseous UF 6 is contained in a mixture of U 235 F 6 and U 238 F 6 molecules in a reaction chamber. A chemically reactive substance, which for U 235 separation may be gaseous HCl according to the invention, is also introduced into the reaction chamber. (HK) [de

  5. Method of isotope separation by chemi-ionization

    International Nuclear Information System (INIS)

    Wexler, S.; Young, C.E.

    1977-01-01

    A method is disclosed for separating isotopes in an isotopic mixture by aerodynamically accelerating a gaseous compound to form a jet of molecules, and passing the jet through a stream of electron donor atoms whereby an electron transfer takes place, thus forming negative ions of the molecules. The molecular ions are then passed through a radiofrequency quadrupole mass filter to separate the specific isotopes. cThis method may be used for any compounds having a sufficiently high electron affinity to permit negative ion formation, and is especially useful for the separation of plutonium and uranium isotopes. 10 claims, 1 figure

  6. Laser alteration of accommodation coefficient for isotope separation

    International Nuclear Information System (INIS)

    Keck, J.C.

    1976-01-01

    This patent describes a method and an apparatus for separating isotope types by inducing an isotopically selective vibrational excitation of molecules containing at least one atom of the element type whose isotopes are to be separated. Vibrational excitation is induced in the molecules by finely tuned, narrow bandwidth laser radiation applied to a gaseous flow of the molecules. Isotopic separation of the molecules is achieved from the enhanced difference in diffusion rates for the molecules due to an alteration of the accommodation coefficients in the excited molecules. 40 claims, 4 figures

  7. Isotopic contamination in electromagnetic isotope separators; La contagion isotopique dans les separateurs electromagnetiques d'isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Cassignol, C [Commissariat a l' Energie Atomique, Saclay (France).Centre d' Etudes Nucleaires

    1960-07-01

    The mechanisms producing isotopic contamination in the electromagnetic separation of isotopes are studied with the aid of the Separator of Saclay and an electrostatic analyzer in cascade. After a separate investigation the result of which is that no contamination comes from the spreading of initial energies of ions, two principal mechanisms are emphasized; scattering and instability of the regime of the sources. The characters of each type of contamination arising from both mechanisms are described in some detail. An unique scheme of isotopic contamination is then derived from the partial ones. This scheme is successfully verified in several experimental separations. The applications concern principally the performances of magnetic cascades and more complex apparatus. It is found that the isotopic purities that such machines can deliver are extremely high. (author) [French] On a etudie, a l'aide du separateur de Saclay et d'un analyseur electrostatique en cascade, les mecanismes par lesquels est produite la contamination isotopique dans la separation electromagnetique des isotopes. A la suite d'une deuxieme etude, qui a mene a la conclusion que la contamination ne provient pas d'une dispersion des energies initiales des ions, on propose deux mecanismes comme etant les plus importants; la diffusion et l'instabilite du regime des sources. On decrit en quelques details la nature de la contamination provenant de deux types de mecanisme. On deduit de ces deux mecanismes un seul schema qui a ete ensuite verifie par plusieurs separations experimentales. Les applications interessent surtout les performances des cascades magnetiques et les appareillages plus complexes. On trouve que les puretes isotopiques que peuvent fournir de tels appareils sont tres elevees. (auteur)

  8. Extraction separation of lithium isotopes with crown-ethers

    International Nuclear Information System (INIS)

    Tsivadze, A.Yu.; Demin, S.V.; Levkin, A.V.; Zhilov, V.I.; Nikol'skij, S.F.; Knyazev, D.A.

    1990-01-01

    By the method of extraction chromatography lithium isotope separation coefficients are measured during chemical isotope exchange between lithium aquocomplex and its complex in chloroform with crown-ethers: benzo-15-crown-5, 15crown-5, dicyclohexano-18-crown-6 and dibenzo-18-crown-6. Lithium perchlorate and trichloroacetate are the salts extracted. Values of 6 Li/ 7 Li isotope separation are 1.0032-1.020

  9. Method and apparatus for isotope separation from a gas stream

    International Nuclear Information System (INIS)

    Szoke, A.

    1978-01-01

    A method and apparatus are described for isotope separation and in particular for separating the desired isotope from the gas in which it is contained by irradiating it with a laser. The laser selectively provides kinetic energy to the isotope through inelastic events, monomolecular or bimolecular, in order to cause it to segregate within or fly out of the gas stream in which it is contained

  10. The Atomic Vapor Laser Isotope Separation Program

    International Nuclear Information System (INIS)

    1992-01-01

    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

  11. Separation of uranium isotopes by selective photoionization

    International Nuclear Information System (INIS)

    Snavely, B.B.; Solarz, R.W.; Tuccio, S.A.

    1975-01-01

    Recent results of experiments on the laser photoseparation of U isotopes are reported. In the first series of experiments a two-step ionization process using a Xe laser to excite the atoms below the ionization level and then a Kr laser to ionize the atoms was described. Under the geometric conditions of the experiment and power of the Kr laser, enrichments between 2.5 and 3 percent were obtained in runs lasting 2 hrs. Calculations to describe the ion trajectories in the collector system reflected the two-band pattern observed on the Be collector plate. A system to study the photoionization process was assembled in which the U beam is excited to a desired energy level with a CW dye laser and an ultraviolet beam intercepts the excited U beam. An analysis of a photoionization spectrum obtained at a resolution of 8 A indicates that the peak cross section for transitions to autoionization states from the 7 M 7 level is large enough to be used in large-scale U separation systems. An ionization value of 6.15 +- 0.2 eV was deduced for the ionization potential of the U atom. (U.S.)

  12. [Atomic Vapor Laser Isotope Separation (AVLIS) program

    International Nuclear Information System (INIS)

    1992-01-01

    This report summarizes work performed for the Atomic Vapor Laser Isotope Separation (AVLIS) program from January through July, 1992. Each of the tasks assigned during this period is described, and results are presented. Section I details work on sensitivity matrices for the UDS relay telescope. These matrices show which combination of mirror motions may be performed in order to effect certain changes in beam parameters. In Section II, an analysis is given of transmission through a clipping aperture on the launch telescope deformable mirror. Observed large transmission losses could not be simulated in the analysis. An EXCEL spreadsheet program designed for in situ analysis of UDS optical systems is described in Section III. This spreadsheet permits analysis of changes in beam first-order characteristics due to changes in any optical system parameter, simple optimization to predict mirror motions needed to effect a combination of changes in beam parameters, and plotting of a variety of first-order data. Optical systems may be assembled directly from OSSD data. A CODE V nonsequential model of the UDS optical system is described in Section IV. This uses OSSD data to build the UDS model; mirror coordinates may thus be verified. Section V summarizes observations of relay telescope performance. Possible procedures which allow more accurate assessment of relay telescope performance are given

  13. Ion implantation by isotope separator on line (ISOL) of indium isotopes

    International Nuclear Information System (INIS)

    Hanada, Reimon; Murayama, Mitsuhiro; Saito, Shigeru; Nagata, Shinji; Yamaguchi, Sadaei; Shinozuka, Tsutomu; Fujioka, Manabu.

    1994-01-01

    111 In has been known as the nuclide which is most suitable to perturbed angular correlation (PAC) process, as the life of its intermediate state is long , the half life is proper in view of the measurement and radiation control, and it is easily available as its chloride is on the market. In the PAC, it is necessary to introduce this probe nuclei into samples. The most simple method is diffusion process, but in the materials, of which the solid-solubility of In is low like Fe and Si, the introduction is very difficult, therefore, it is necessary to do ion implantation. The development of this process was tried, and the results are reported. For the experiment, the ISOL in the cyclotron RI center, Tohoku University, was used as the accelerator for the implantation. The experimental method is explained. As the results, in the case of nonradioactive In implantation, the Ruthereford back scattering (RBS) spectra of the Si in which In was implanted, the spectra when the channeling condition was satisfied, and the results of measuring the angle dependence of channeling for In and In-implanted Si are shown. In the case of the ion implantation of radioactive 111 In, the energy spectra of In-implanted Si, the PAC spectra of In-implanted Si samples, and the PAC spectra for pure iron and Fe-Si alloy are shown. The further improvement of the ion sources is necessary. (K.I.)

  14. Isotope separation by selective photodissociation of glyoxal

    International Nuclear Information System (INIS)

    Marling, J.B.

    1976-01-01

    Dissociation products, mainly formaldehyde and carbon monoxide, enriched in a desired isotope of carbon, oxygen, or hydrogen are obtained by the selective photodissociation of glyoxal wherein glyoxal is subjected to electromagnetic radiation in a predetermined wavelength such that photon absorption excites and induces dissociation of only those molecules of glyoxal containing the desired isotope

  15. Aerodynamic isotope separation processes for uranium enrichment: process requirements

    International Nuclear Information System (INIS)

    Malling, G.F.; Von Halle, E.

    1976-01-01

    The pressing need for enriched uranium to fuel nuclear power reactors, requiring that as many as ten large uranium isotope separation plants be built during the next twenty years, has inspired an increase of interest in isotope separation processes for uranium enrichment. Aerodynamic isotope separation processes have been prominently mentioned along with the gas centrifuge process and the laser isotope separation methods as alternatives to the gaseous diffusion process, currently in use, for these future plants. Commonly included in the category of aerodynamic isotope separation processes are: (a) the separation nozzle process; (b) opposed gas jets; (c) the gas vortex; (d) the separation probes; (e) interacting molecular beams; (f) jet penetration processes; and (g) time of flight separation processes. A number of these aerodynamic isotope separation processes depend, as does the gas centrifuge process, on pressure diffusion associated with curved streamlines for the basic separation effect. Much can be deduced about the process characteristics and the economic potential of such processes from a simple and elementary process model. In particular, the benefit to be gained from a light carrier gas added to the uranium feed is clearly demonstrated. The model also illustrates the importance of transient effects in this class of processes

  16. Environmental readiness document advanced isotope separation program

    International Nuclear Information System (INIS)

    1981-08-01

    Advanced Isotope Separation (AIS) techniques hold the promise of significantly reducing the cost of enriching uranium for use in commercial nuclear power reactors. By reducing uranium enrichment costs, the tails assay of an enrichment plant can be lowered resulting in a decrease in the requirements for natural uranium feed material and a small decrease in the cost of the electricity produced by nuclear power plants. With this increased efficiency of uranium enrichment, there will be an overall reduction in the environmental impacts associated with uranium processing in the front end of the fuel cycle. AIS is characterized by much lower energy requirements compared to diffusion; comparable energy requirements to centrifuge; generally similar offsite environmental and socioeconomic impacts to centrifuge; and substantially fewer secondary impacts than diffusion because of reduced need for power. In the broadest definitions of environmental concerns, the socio-political and security aspects of proliferation and safeguards are the most significant in reducing AIS to practice. The potential exists for exposure of plant workers or offsite personnel to radioactive material or process chemical during normal or accident conditions. Some AIS processes make use of strong magnetic or electromagnetic fields and lasers, and methods are required to monitor the levels of these radiations. The AIS processes will routinely generate chemical and radioactive wastes. Additional wastes may be generated during plant decontamination and decommissioning. All of these wastes must be managed to meet Federal and state requirements. Finally, based on preliminary designs, some of the AIS processes may require significant, relative to US and world supply, quantities of a coating material

  17. Separation efficiency of the MASHA facility for short-lived mercury isotopes

    Science.gov (United States)

    Rodin, A. M.; Belozerov, A. V.; Chernysheva, E. V.; Dmitriev, S. N.; Gulyaev, A. V.; Gulyaeva, A. V.; Itkis, M. G.; Kliman, J.; Kondratiev, N. A.; Krupa, L.; Novoselov, A. S.; Oganessian, Yu. Ts.; Podshibyakin, A. V.; Salamatin, V. S.; Siváček, I.; Stepantsov, S. V.; Vanin, D. V.; Vedeneev, V. Yu.; Yukhimchuk, S. A.; Granja, C.; Pospisil, S.

    2014-06-01

    The mass-separator MASHA built to identify Super Heavy Elements by their mass-to-charge ratios is described. The results of the off- and on-line measurements of its separation efficiency are presented. In the former case four calibrated leaks of noble gases were used. In the latter the efficiency was measured via 284 MeV Ar beam and with using the hot catcher. The ECR ion source was used in both cases. The -radioactive isotopes of mercury produced in the complete fusion reaction Ar+SmHg+xn were detected at the mass-separator focal plane. The half-lives and the separation efficiency for the short-lived mercury isotopes were measured. Potentialities of the MEDIPIX detector system have been demonstrated for future use at the mass-separator MASHA.

  18. Stable isotope separation; Separations physicochimiques d'isotopes stables realisations et etudes de petites productions

    Energy Technology Data Exchange (ETDEWEB)

    Botter, F; Molinari, Ph; Dirian, G [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1964-07-01

    Pure deuterium has been separated from gaseous mixtures of hydrogen and deuterium by band displacement chromatography, using columns of palladium on a support. The best results were obtained with columns of Pd on sintered {alpha} alumina. With a column of this type, of total capacity about 2 liters, a preparative apparatus of low dead volume has been built which produces 1 liter of pure D{sub 2} from a 50 p. 100 D{sub 2}, 50 p. 100 100 H{sub 2} mixture in about 12 minutes. As a first approximation chromatography is likened theoretically to counter current fractionation, neglecting superficial resistance to the exchange. and also longitudinal diffusions. The number of theoretical plates required necessary for a certain enrichment of the gas phase is determined graphically or by calculation, enabling comparisons to be made between the efficiencies of columns containing different amounts of palladium. Thermal Diffusion: For the separation of hydrogen isotopes a thermal diffusion installation, made of stainless steel and entirely tele-commanded has been constructed. The separation cascade is made up of two identical pairs of hot wire columns. Each pair can work separately or they may be connected by a thermosyphon. The temperature of the hot wire is kept at around 1000 deg C by direct current. With this installation, hydrogen samples with a deuterium content lower than o,5 ppm were obtained from a gas originally containing 32 ppm. It was thus possible to prepare tritium of 99,3 p. 100 concentration from gas with an initial content of 6 p. 100. For quantitative separation of xenon enriched five time in {sup 124}Xe by thermal diffusion, two identical cascades were constructed, each consisting of 5 columns, working in parallel and the two being connected by thermosyphon or by a capillary tube linked to a thermal gas oscillation. The central tungsten wire is heated to 1200 deg C. The columns are grouped like cluster of a heat exchanger, in shell of 30 cm diameter through

  19. Investigation of gas discharge ion sources for on-line mass separation

    International Nuclear Information System (INIS)

    Kirchner, R.

    1976-03-01

    The development of efficient gas discharge ion sources with axial beam extraction for on-line mass separation is described. The aim of the investigation was to increase the ion source temperature, the lifetime and the ionisation yield in comparison to present low-pressure are discharge ion sources and to reduce the ion current density from usually 1 to 100 mA/cm 3 . In all ion sources the pressure range below the minimal ignition pressure of the arc discharge was investigated. As a result an ion source was developed which works at small changes in geometry and in electric device of a Nielsen source with high ionization yield (up to 50% for xenon) stabil and without ignition difficulties up to 10 -5 Torr. At a typical pressure of 3 x 10 -5 Torr ion current and ion current density are about 1 μA and 0.1 mA/cm 3 respectively besides high yield and a great emission aperture (diameter 1.2 mm). (orig.) [de

  20. Laser spectroscopy and laser isotope separation of atomic gadolinium

    International Nuclear Information System (INIS)

    Chen, Y. W.; Yamanaka, C.; Nomaru, K.; Kou, K.; Niki, H.; Izawa, Y.; Nakai, S.

    1994-01-01

    Atomic vapor laser isotope separation (AVLIS) is a process which uses intense pulsed lasers to selectively photoionize one isotopic species of a chemical element, after which these ions are extracted electromagnetically. The AVLIS has several advantages over the traditional methods based on the mass difference, such as high selectivity, low energy consumption, short starting time and versatility to any atoms. The efforts for atomic vapor laser isotope separation at ILT and ILE, Osaka University have been concentrated into the following items: 1) studies on laser spectroscopy and laser isotope separation of atomic gadolinium, 2) studies on interaction processes including coherent dynamics, propagation effects and atom-ion collision in AVLIS system, 3) development of laser systems for AVLIS. In this paper, we present experimental results on the laser spectroscopy and laser isotope separation of atomic gadolinium.

  1. Combined electrolysis catalytic exchange (CECE) process for hydrogen isotope separation

    International Nuclear Information System (INIS)

    Hammerli, M.; Stevens, W.H.; Butler, J.P.

    1978-01-01

    Hydrogen isotopes can be separated efficiently by a process which combines an electrolysis cell with a trickle bed column packed with a hydrophobic platinum catalyst. The column effects isotopic exchange between countercurrent streams of electrolytic hydrogen and liquid water while the electrolysis cell contributes to isotope separation by virtue of the kinetic isotope effect inherent in the hydrogen evolution reaction. The main features of the CECE process for heavy water production are presented as well as a discussion of the inherent positive synergistic effects, and other advantages and disadvantages of the process. Several potential applications of the process in the nuclear power industry are discussed. 3 figures, 2 tables

  2. On-line coupling of the MAT 251 with a Carlo Erba elemental analyzer for carbon isotope ratio measurements

    International Nuclear Information System (INIS)

    Pichlmayer, F.

    1986-06-01

    For carbon isotope investigations with a moderate precision demand of about 0.2 per mil in the isotope ratio fast and reliable results are attained by on line combination of the ANA 1500 Elemental Analyzer and the MAT 251 Isotope Mass Spectrometer. The crucial point hereof is the gas splitting device. By proper design and adjustment of the analytical parameters, good sample efficiency and a sharp CO 2 bulk within the He stream is reached. The main characteristics of this combined equipment are described and some isotopic results of organic and anorganic carbon in lake sediment-samples are given as well as deltasup1 3 C-analyses of spiritous liquors. (Author)

  3. Production of chemically reactive radioactive ion beams through on-line separation; Production de faisceaux d'ions radioactifs chimiquement reactifs par separation en ligne

    Energy Technology Data Exchange (ETDEWEB)

    Joinet, A

    2003-10-01

    The ISOL (isotope separation on line) allows the production of secondary radioactive ion beams through spallation or fragmentation or fission reactions that take place in a thick target bombarded by a high intensity primary beam. The challenge is to increase the intensity and purity of the radioactive beam. The optimization of the system target/source requires the right choice of material for the target by taking into account the stability of the material, its reactivity and the ionization method used. The target is an essential part of the system because radioactive elements are generated in it and are released more or less quickly. Tests have been made in order to select the best fitted material for the release of S, Se, Te, Ge and Sn. Materials tested as target filling are: ZrO{sub 2}, Nb, Ti, V,TiO{sub 2}, CeO{sub x}, ThO{sub 2}, C, ZrC{sub 4} and VC). Other molecules such as: COSe, COS, SeS, COTe, GeS, SiS, SnS have been studied to ease the extraction of recoil nuclei (Se, S, Te, Ge and Sn) produced inside the target.

  4. Production of chemically reactive radioactive ion beams through on-line separation; Production de faisceaux d'ions radioactifs chimiquement reactifs par separation en ligne

    Energy Technology Data Exchange (ETDEWEB)

    Joinet, A

    2003-10-01

    The ISOL (isotope separation on line) allows the production of secondary radioactive ion beams through spallation or fragmentation or fission reactions that take place in a thick target bombarded by a high intensity primary beam. The challenge is to increase the intensity and purity of the radioactive beam. The optimization of the system target/source requires the right choice of material for the target by taking into account the stability of the material, its reactivity and the ionization method used. The target is an essential part of the system because radioactive elements are generated in it and are released more or less quickly. Tests have been made in order to select the best fitted material for the release of S, Se, Te, Ge and Sn. Materials tested as target filling are: ZrO{sub 2}, Nb, Ti, V,TiO{sub 2}, CeO{sub x}, ThO{sub 2}, C, ZrC{sub 4} and VC). Other molecules such as: COSe, COS, SeS, COTe, GeS, SiS, SnS have been studied to ease the extraction of recoil nuclei (Se, S, Te, Ge and Sn) produced inside the target.

  5. Simplified simulation of multicomponent isotope separation by gas centrifuge

    International Nuclear Information System (INIS)

    Guo Zhixiong; Ying Chuntong

    1995-01-01

    The expressions of diffusion equation for multicomponent isotope separation by gas centrifuge are derived by utilizing the simplified diffusion transport vector. A method of radial averaging which was restricted to a binary mixture is extended to multicomponent isotope mixtures by using an iterative scheme. A numerical analysis of tetradic UF 6 or SF 6 gas isotope separation by centrifuge is discussed when a special model of velocity distribution is given. The dependence of mutual separation factor for the components on their molecular weights' difference is obtained. Some aspects of the given model of gas fluid are also discussed

  6. Process for separating U isotopes by infrared excitation

    International Nuclear Information System (INIS)

    Lyon, R.K.; Kaldor, Andrew.

    1976-01-01

    This invention concerns a process for separating a substance into at least two parts in which the isotopic abundances of a given element differ from those of the isotopes of the substance prior to separation. Specifically, the invention concerns a process for the selective excitation of the isotopes of a gaseous phase UF 6 by absorption of infra-red photons, then by selective reaction of UF 6 excited with atomics chlorine, bromine or iodine, forming a product that may be separated by a standard method. The preference criteria of the atomic chlorine, bromine and iodine are related to the thermal dilution problem [fr

  7. Isotope separation by photodissociation of Van der Wall's molecules

    International Nuclear Information System (INIS)

    Lee, Y.T.

    1977-01-01

    A method of separating isotopes based on the dissociation of a Van der Waal's complex is described. 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

  8. Mathematical Modeling of Nonstationary Separation Processes in Gas Centrifuge Cascade for Separation of Multicomponent Isotope Mixtures

    OpenAIRE

    Orlov Alexey; Ushakov Anton; Sovach Victor

    2016-01-01

    This article presents results of development of the mathematical model of nonstationary separation processes occurring in gas centrifuge cascades for separation of multicomponent isotope mixtures. This model was used for the calculation parameters of gas centrifuge cascade for separation of germanium isotopes. Comparison of obtained values with results of other authors revealed that developed mathematical model is adequate to describe nonstationary separation processes in gas centrifuge casca...

  9. Analysis and separation of boron isotopes; Analyse et separation des isotopes du bore

    Energy Technology Data Exchange (ETDEWEB)

    Perie, M [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1966-11-01

    The nuclear applications of boron-10 justify the study of a method of measurement of its isotopic abundance as well as of very small traces of boron in different materials. A systematic study of thermionic emission of BO{sub 2}Na{sub 2}{sup +} has been carried out. In the presence of a slight excess of alkalis, the thermionic emission is considerably reduced. On the other hand, the addition of a mixture of sodium hydroxide-glycerol (or mannitol) to borax permits to obtain an intense and stable beam. These results have permitted to establish an operative method for the analysis of traces of boron by isotopic dilution. In other respects, the needs of boron-10 in nuclear industry Justify the study of procedures of separation of isotopes of boron. A considerable isotopic effect has been exhibited in the chemical exchange reaction between methyl borate and borate salt in solution. In the case of exchange between methyl borate and sodium borate, the elementary separation factor {alpha} is: {alpha}=(({sup 11}B/{sup 10}B)vap.)/(({sup 11}B/{sup 10}B)liq.)=1.03{sub 3}. The high value of this elementary effect has been multiplied in a distillation column in which the problem of regeneration of the reactive has been resolved. An alternative procedure replacing the alkali borate by a borate of volatile base, for example diethylamine, has also been studied ({alpha}=1,02{sub 5} in medium hydro-methanolic with 2,2 per cent water). (author) [French] Les applications nucleaires du bore 10 justifient l'etude d'une methode de mesure de son abondance isotopique dans divers materiaux ainsi que le dosage de tres faibles traces de bore. Une etude systematique de l'emission thermoionique de BO{sub 2} Na{sub 2}{sup +} a ete effectuee. En presence d'un leger exces d'alcalins, l'emission thermoionique est considerablement reduite. Par contre l'addition au borax d'un melange soude-glycerol (ou mannitol) permet d'obtenir un faisceau stable et intense. Ces resultats ont permis d'etablir un mode

  10. Chemical exchange equilibria in isotope separation. Part I : Evaluation of separation factors

    International Nuclear Information System (INIS)

    Dave, S.M.

    1980-01-01

    The theory of chemical exchange equilibria as applied to the isotope separation processes and the isotope effects on equilibrium constants of different exchange reactions has come a long way since its inception by Urey and Rittenberg. An attempt has been made to bring relevant information together and present a unified approach to isotopic chemical exchange equilibrium constant evaluation and its implications to separation processes. (auth.)

  11. Process and device for U isotope separation

    International Nuclear Information System (INIS)

    Aubert, Jacques; Carles, Maurice; Neige, Roger.

    1976-01-01

    The description is given of a process for enriching uranium with one of its isotopes by isotopic exchange in sub-cascades assembled to form a cascade, each sub-cascade having facilities for bringing into contact an aqueous phase charged with uranium of a lower valency with an organic phase charged with uranium of a higher valency, in conditions that restrict the transfer of upper valency uranium into the aqueous phase. Each sub-cascade has the following stages at least: isotopic exchange in a set of contact systems between the aqueous phase and the organic phase where the aqueous phase depletes and the organic phase becomes enriched with isotope 235; uranium extraction until depletion of the organic phase in a first extractor; reduction of the liquid phase uranium and acidification before this reduced aqueous phase passes into the isotopic exchange system then oxidation of the uranium of this aqueous phase coming from the system; extraction of the aqueous phase uranium until depletion in the second extractor by the organic phase [fr

  12. Laser isotope separation - a new class of chemical process

    International Nuclear Information System (INIS)

    Woodall, K.B.; Mannik, L.; O'Neill, J.A.; Mader, D.L.; Nickerson, S.B.; Robins, J.R.; Bartoszek, F.E.; Gratton, D.

    1983-01-01

    Lasers may soon find several applications in chemical processing. The applications that have attracted the most research funding to date involve isotope separation for the nuclear industry. These isotopes have an unusually high value (≥$1000/kg) compared to bulk chemicals (∼$1/kg) and are generally required in very large quantities. In a laser isotope separation process, light is used to convert a separation that is very difficult or even impossible by conventional chemical engineering techniques to one that is readily handled by conventional separation technology. For some isotopes this can result in substantial capital and energy savings. A uranium enrichment process developed at the Lawrence Livermore National Laboratory is the closest to commercialization of the large scale laser isotope separation processes. Of particular interest to the Canadian nuclear industry are the laser separation of deuterium, tritium, zirconium-90 and carbon-14. In this paper, the basic principles behind laser isotope separation are reviewed and brief dscriptions of the more developed processes are given

  13. Lasers for the SILVA laser isotope separation process

    International Nuclear Information System (INIS)

    Lapierre, Y.

    1997-01-01

    The main principles of the laser isotope separation process for the production of enriched uranium at lower cost, are reviewed and the corresponding optimal laser characteristics are described. The development of the SILVA laser isotope separation process involved researches in the various domains of pump lasers, dye lasers, laser and optics systems and two test facilities for the feasibility studies which are expected for 1997

  14. Energy expenditures of plasma method of isotope separation

    International Nuclear Information System (INIS)

    Karchevskij, A.I.; Potanin, E.P.

    1986-01-01

    The estimations are performed of specific energy expenditares in isotope separation of binary mixtures in different plasma systems with weak medium ionization (plasma centrifuge, gas discharge system with travelling magnetic field, direct current discharge). Potential advantages of plasma centrifuge over other gas discharge facilities are pointed out. The comparison of specific energy expenditure values in case of using plasma and conventional methods of isotope separation is carried out

  15. Thermal diffusion and separation of isotopes; Diffusion thermique et separation d'isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Fournier, Andre

    1944-03-30

    After a review of the various processes used to separate isotopes or at least to obtain mixes with a composition different from the natural proportion, this research addresses the use of thermal diffusion. The author reports a theoretical study of gas thermal diffusion and of the Clusius-Dickel method. In the second part, he reports the enrichment of methane with carbon-13, and of ammoniac with nitrogen-15. The next part reports the experimental study of thermal diffusion of liquids and solutions, and the enrichment of carbon tetra-chloride with chlorine-37. The author then proposes an overview of theories of thermal diffusion in liquid phase (hydrodynamic theory, kinetic theory, theory of caged molecules)

  16. On-line double isotope dilution laser ablation inductively coupled plasma mass spectrometry for the quantitative analysis of solid materials.

    Science.gov (United States)

    Fernández, Beatriz; Rodríguez-González, Pablo; García Alonso, J Ignacio; Malherbe, Julien; García-Fonseca, Sergio; Pereiro, Rosario; Sanz-Medel, Alfredo

    2014-12-03

    We report on the determination of trace elements in solid samples by the combination of on-line double isotope dilution and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). The proposed method requires the sequential analysis of the sample and a certified natural abundance standard by on-line IDMS using the same isotopically-enriched spike solution. In this way, the mass fraction of the analyte in the sample can be directly referred to the certified standard so the previous characterization of the spike solution is not required. To validate the procedure, Sr, Rb and Pb were determined in certified reference materials with different matrices, including silicate glasses (SRM 610, 612 and 614) and powdered samples (PACS-2, SRM 2710a, SRM 1944, SRM 2702 and SRM 2780). The analysis of powdered samples was carried out both by the preparation of pressed pellets and by lithium borate fusion. Experimental results for the analysis of powdered samples were in agreement with the certified values for all materials. Relative standard deviations in the range of 6-21% for pressed pellets and 3-21% for fused solids were obtained from n=3 independent measurements. Minimal sample preparation, data treatment and consumption of the isotopically-enriched isotopes are the main advantages of the method over previously reported approaches. Copyright © 2014 Elsevier B.V. All rights reserved.

  17. The on-line graph processing study on phase separation of two-phase flow in T-tube

    International Nuclear Information System (INIS)

    Qian Yong; Xu Jijun; Yang Zhilin; Chen Yifen

    1997-01-01

    The on-line graph processing measure system is equipped with and experimental study of phase separation of air-water bubbly flow in the horizontal T-junction is carried out. For the first time, the author have found and defined the new type of complete phase separation, by the visual experiment, which shows that under certain conditions, the air flow entering the T junction will flow into the run outlet completely, which had never been reported in the literature Also, the pressure wave feed back effect and the branch bubble flow reorganization effect were found and analyzed. The complexity of this phase separation phenomenon in the T junction has been further revealed via the on-line graph processing technology. Meanwhile the influences of the inlet mass flow rate W1, the inlet mass quality X1, and the mass extraction rate G3/G1 on phase separation were analyzed

  18. Laser isotope and isomer separations: History and trends

    International Nuclear Information System (INIS)

    Letok'ov, V.S.

    1990-01-01

    Paper will review history and principles of laser isotope and nuclear isomer separation: laser multistep photoionization of isotopic and isomeric atoms, laser IR-UV two-step photodissociation of molecules, laser IR multiphoton photodissociation of polyatomic molecules. The comparison and areas of applications of these methods will be considered. Paper will discuss a present state of art of technology of these methods in practical scale in various countries. In conclusion the trends of research in this field including applications of laser-separated isotopes and isomers will be considered

  19. Development of O-18 stable isotope separation technology using membrane

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Jae Woo; Kim, Taek Soo; Choi, Hwa Rim; Park, Sung Hee; Lee, Ki Tae; Chang, Dae Shik

    2006-06-15

    The ultimate goal of this investigation is to develop the separation technology for O-18 oxygen stable isotope used in a cyclotron as a target for production of radioisotope F-18. F-18 is a base material for synthesis of [F-18]FDG radio-pharmaceutical, which is one of the most important tumor diagnostic agent used in PET (Positron Emission Tomography). More specifically, this investigation is focused on three categories as follow, 1) development of the membrane distillation isotope separation process to re-enrich O-18 stable isotope whose isotopic concentration is reduced after used in a cyclotron, 2) development of organic impurity purification technology to remove acetone, methanol, ethanol, and acetonitrile contained in a used cyclotron O-18 enriched target water, and 3) development of a laser absorption spectroscopic system for analyzing oxygen isotopic concentration in water.

  20. On line spectrophotometry with optical fibers. Application to uranium-plutonium separation in a spent fuel reprocessing plant

    International Nuclear Information System (INIS)

    Boisde, G.; Mus, G.; Tachon, M.

    1985-06-01

    Optimization of mixer-settler operation for uranium-plutonium separation in the Purex process can be obtained by remote spectrophotometry with optical fibers. Data acquisition on uranium VI, uranium IV and plutonium III is examined in function of acidity and nitrate content of the solution. Principles for on line multicomponent monitoring and mathematical modelization of the measurements are described [fr

  1. Experimental study of stable isotope separation

    International Nuclear Information System (INIS)

    Mingsheng Zhou; Chuntong Ying; Yuguang Nie

    1999-01-01

    This paper presents some results of investigation into a gas centrifuge and gas centrifuge cascade. The chemical compounds of osmium - OsO 4 , tungsten - WF 6 and xenon were chosen for centrifugal separation, and the centrifugal technology for the separation of osmium, tungsten and xenon were developed. The separation factors for molar mass differences, γ 0 , were obtained for OsO 4 , Xe, WF 6 in a single gas centrifuge. The separation by gas centrifuge cascade has been done and some results of the investigation are shown. High abundance of 186 W (>90 %), 129 Xe (>65 %) and 192 Os (>99 %) was produced using the short cascade [ru

  2. Separation and preparation of "6"2Ni isotope

    International Nuclear Information System (INIS)

    Ren Xiuyan; Mi Yajing; Zeng Ziqiang; Li Gongliang; Tu Rui

    2014-01-01

    Micro nuclear battery is the perfect power of space craft equipment. "6"3Ni is the core operation material of the "6"3Ni battery. It can produce radioisotope "6"3Ni while high abundance "6"2Ni is irradiated in the reactor. In order to meet the requirements of the abundance and the purity, research of the separation for "6"2Ni isotope was developed. The magnetic field and beam transmission status were simulated. The improvement designs of the ion source and the collector pocket were carried out. The process flow of high abundance "6"2Ni using electromagnetic separation method was established. The experiment of "6"2Ni isotope was developed by using electromagnetism isotope separator. The results show that the enrichment of "6"2Ni isotope is more than 90%. (authors)

  3. Selective heating and separation of isotopes in a metallic plasma

    International Nuclear Information System (INIS)

    Moffa, P.; Cheshire, D.; Flanders, B.; Myer, R.; Robinette, W.; Thompson, J.; Young, S.

    1983-01-01

    Several types of metallic plasmas have been produced at the Plasma Separation Process facility of TRW. Selective heating and separation of specific isotopes in these plasmas have been achieved. In this presentation the authors concentrate on the modeling of the selective heating and separation of the isotope Ni 58 . Two models are currently used to describe the excitation process. In both, the electromagnetic fields in the plasma produced by the ICRH antenna are calculated self-consistently using a kinetic description of the warm plasma dielectric. In the Process Model Code, both the production of the plasma and the heating are calculated using a Monte Carlo approach. Only the excitation process is treated in the second simplified model. Test particles that sample an initial parallel velocity distribution are launched into the heating region and the equations of motion including collisional damping are calculated. For both models, the perpendicular energy for a number of particles with different initial conditions and representing the different isotopes is calculated. This information is then input into a code that models the performance of our isotope separation collector. The motion of the ions of each isotope through the electrically biased collector is followed. An accounting of where each particle is deposited is kept and hence the isotope separation performance of the collector is predicted

  4. Basic separative power of multi-component isotopes separation in a gas centrifuge

    International Nuclear Information System (INIS)

    Jiang, Hongmin; Lei, Zengguang; Zhuge, Fu

    2008-01-01

    On condition that the overall separation factor per unit exists in centrifuge for multi-component isotopes separation, the relations between separative power of each component and molecular weight have been investigated in the paper while the value function and the separative power of binary-component separation are adopted. The separative power of each component is proportional to the square of the molecular weight difference between its molecular weight and the average molecular weight of other remnant components. In addition, these relations are independent on the number of the components and feed concentrations. The basic separative power and related expressions, suggested in the paper, can be used for estimating the separative power of each component and analyzing the separation characteristics. The most valuable application of the basic separative power is to evaluate the separative capacity of centrifuge for multi-component isotopes. (author)

  5. Design of the Advanced Rare Isotope Separator ARIS at FRIB

    Energy Technology Data Exchange (ETDEWEB)

    Hausmann, M., E-mail: hausmann@frib.msu.edu [Facility for Rare Isotope Beams, Michigan State University, East Lansing, MI 48824 (United States); Aaron, A.M. [Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States); Amthor, A.M. [Dept. of Physics and Astronomy, Bucknell University, Lewisburg, PA 17837 (United States); Avilov, M.; Bandura, L.; Bennett, R.; Bollen, G.; Borden, T. [Facility for Rare Isotope Beams, Michigan State University, East Lansing, MI 48824 (United States); Burgess, T.W. [Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States); Chouhan, S.S. [Facility for Rare Isotope Beams, Michigan State University, East Lansing, MI 48824 (United States); Graves, V.B. [Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States); Mittig, W. [Facility for Rare Isotope Beams, Michigan State University, East Lansing, MI 48824 (United States); National Superconducting Cyclotron Laboratory, Michigan State University, East Lansing, MI 48824 (United States); Morrissey, D.J. [National Superconducting Cyclotron Laboratory, Michigan State University, East Lansing, MI 48824 (United States); Pellemoine, F.; Portillo, M.; Ronningen, R.M.; Schein, M. [Facility for Rare Isotope Beams, Michigan State University, East Lansing, MI 48824 (United States); Sherrill, B.M. [Facility for Rare Isotope Beams, Michigan State University, East Lansing, MI 48824 (United States); National Superconducting Cyclotron Laboratory, Michigan State University, East Lansing, MI 48824 (United States); Zeller, A. [Facility for Rare Isotope Beams, Michigan State University, East Lansing, MI 48824 (United States)

    2013-12-15

    The Facility for Rare Isotopes Beams (FRIB) at Michigan State University will use projectile fragmentation and induced in-flight fission of heavy-ion primary beams at energies of 200 MeV/u and higher and at a beam power of 400 kW to generate rare isotope beams for experiments in nuclear physics, nuclear astrophysics, and fundamental symmetries, as well as for societal needs. The Advanced Rare Isotope Separator (ARIS) has been designed as a three-stage fragment separator for the efficient collection and purification of the rare isotope beams of interest. A vertically bending preseparator (first stage) with production target and beam dump is fully integrated into a production target facility hot cell with remote handling. The new separator compresses the accepted momentum width of up to ±5% of the beam by a factor of three in the standard operational mode. Provisions for alternate operational modes for specific cases are included in the design. This preseparator is followed by two, horizontally-bending separator stages (second and third stages) utilizing the magnets from the existing A1900 fragment separator at the National Superconducting Cyclotron Laboratory (NSCL). These stages can alternatively be coupled to a single high-resolution separator stage, resulting in the flexibility to optimize the operation for different experiments, including momentum tagging and in-flight particle identification of rare isotope beams. The design of ARIS will be presented with an emphasis on beam physics characteristics, and anticipated operational modes will be described.

  6. Cascades for hydrogen isotope separation using metal hydrides

    International Nuclear Information System (INIS)

    Hill, F.B.; Grzetic, V.

    1982-01-01

    Designs are presented for continuous countercurrent hydrogen isotope separation cascades based on the use of metal hydrides. The cascades are made up of pressure swing adsorption (PSA) or temperature swing adsorption (TSA) stages. The designs were evolved from consideration of previously conducted studies of the separation performance of four types of PSA and TSA processes

  7. Cascades for hydrogen isotope separation using metal hydrides

    Energy Technology Data Exchange (ETDEWEB)

    Hill, F B; Grzetic, V [Brookhaven National Lab., Upton, NY (USA)

    1983-02-01

    Designs are presented for continuous countercurrent hydrogen isotope separation cascades based on the use of metal hydrides. The cascades are made up of pressure swing adsorption (PSA) or temperature swing adsorption (TSA) stages. The designs were evolved from consideration of previously conducted studies of the separation performance of four types of PSA and TSA processes.

  8. Germanium-76 Isotope Separation by Cryogenic Distillation. Final Report

    International Nuclear Information System (INIS)

    Stohler, Eric

    2007-01-01

    The current separation method for Germanium isotopes is electromagnetic separation using Calutrons. The Calutrons have the disadvantage of having a low separation capacity and a high energy cost to achieve the separation. Our proposed new distillation method has the advantage that larger quantities of Germanium isotopes can be separated at a significantly lower cost and in a much shorter time. After nine months of operating the column that is 1.5 meter in length, no significant separation of the isotopes has been measured. We conclude that the length of the column we have been using is too short. In addition, other packing material than the 0.16 inch Propak, 316 ss Protruded metal packing that we used in the column, should be evaluated which may have a better separation factor than the 0.16 inch Propak, 316 ss Protruded metal packing that has been used. We conclude that a much longer column - a minimum of 50 feet length - should be built and additional column packing should be tested to verify that isotopic separation can be achieved by cryogenic distillation. Even a longer column than 50 feet would be desirable.

  9. Low energy methods of molecular laser isotope separation

    International Nuclear Information System (INIS)

    Makarov, G N

    2015-01-01

    Of the many proposals to date for laser-assisted isotope separation methods, isotope-selective infrared (IR) multiphoton dissociation (MPD) of molecules has been the most fully developed. This concept served as the basis for the development and operation of the carbon isotope separation facility in Kaliningrad, Russia. The extension of this method to heavy elements, including uranium, is hindered by, among other factors, the high power consumption and the lack of high-efficiency high-power laser systems. In this connection, research and development covering low energy methods for the laser separation of isotopes (including those of heavy atoms) is currently in high demand. This paper reviews approaches to the realization of IR-laser-induced isotope-selective processes, some of which are potentially the basis on which low-energy methods for molecular laser isotope separation can be developed. The basic physics and chemistry, application potential, and strengths and weaknesses of these approaches are discussed. Potentially promising alternatives to the title methods are examined. (reviews of topical problems)

  10. Isotope separation utilizing Zeeman compensated magnetic extraction

    International Nuclear Information System (INIS)

    Forsen, H.K.

    1978-01-01

    A vapor flow of elemental uranium is directed into a region where narrow band, tuned laser radiation is repeatedly applied to provide at least two energy step selective ionization of the U 235 isotope in the vapor flow. A magnetic field is applied in the region of the ionized U 235 which creates a Lorentz force on the moving ions directing them toward one of a plurality of collection plates placed generally parallel to the vapor flow to permit collection of the U 235 particles in substantially enriched proportions as compared to the concentration in the vapor flow generally. To prevent a broadening of the absorption lines for both the U 235 and U 238 isotopes in the vapor flow from the applied magnetic field and thus prevent substantial reduction in the selectivity of the excitation and ionization, the magnetic field is preferably applied in a time varying magnitude which is phased with respect to the repetitive application of laser radiation to provide a relatively low field strength and corresponding small Zeeman splitting during selective excitation and ionization of the U 235 particles

  11. Production of stable isotopes utilizing the plasma separation process

    Science.gov (United States)

    Bigelow, T. S.; Tarallo, F. J.; Stevenson, N. R.

    2005-12-01

    A plasma separation process (PSP) is being operated at Theragenics Corporation's®, Oak Ridge, TN, facility for the enrichment of stable isotopes. The PSP utilizes ion cyclotron mass discrimination to separate isotopes on a relatively large scale. With a few exceptions, nearly any metallic element could be processed with PSP. Output isotope enrichment factor depends on natural abundance and mass separation and can be fairly high in some cases. The Theragenics™ PSP facility is believed to be the only such process currently in operation. This system was developed and formerly operated under the US Department of Energy Advanced Isotope Separation program. Theragenics™ also has a laboratory at the PSP site capable of harvesting the isotopes from the process and a mass spectrometer system for analyzing enrichment and product purity. Since becoming operational in 2002, Theragenics™ has utilized the PSP to separate isotopes of several elements including: dysprosium, erbium, gadolinium, molybdenum and nickel. Currently, Theragenics™ is using the PSP for the separation of 102Pd, which is used as precursor for the production of 103Pd. The 103Pd radioisotope is the active ingredient in TheraSeed®, which is used in the treatment of early stage prostate cancer and being investigated for other medical applications. New industrial, medical and research applications are being investigated for isotopes that can be enriched on the PSP. Pre-enrichment of accelerator or reactor targets offers improved radioisotope production. Theragenics operates 14 cyclotrons for proton activation and has access to HFIR at ORNL for neutron activation of radioisotopes.

  12. Uranium-isotope enrichment: application bounds of the separative power and separation work concepts

    Energy Technology Data Exchange (ETDEWEB)

    Novelli, P.

    1981-05-01

    The aim of this paper is a critical re-examination of the concepts of separative power, separation work and value function in order to understand if their extension to the new enrichment processes such as Laser Isotope Separation is possible.

  13. Gas-chromatographic separation of hydrogen isotopic mixtures

    International Nuclear Information System (INIS)

    Preda, Anisoara; Bidica, Nicolae

    2005-01-01

    Full text: Gas chromatographic separation of hydrogen isotopes have been reported in the literature since late of 1950's. Gas chromatography is primarily an analytical method, but because of its properties it may be used in many other fields with excellent results. A simple method is proposed for the gas-chromatographic analysis of complex gas mixtures containing hydrogen isotopes; the method is based on the substantial difference in the thermal conductivity of these isotopes. One of the main disadvantages of the conventional gas chromatography is the long retention times required for the analysis of hydrogen gas mixtures while the column is operated at very low temperature. The method described in this paper was based on using a capillary molecular sieve 5A column operated for this kind of separation at 173 K. The carrier gas was Ne and the detector was TCD. In the paper chromatograms for various carrier flow rates and various hydrogen isotope mixtures are presented. (authors)

  14. Method of deuterium isotope separation and enrichment

    International Nuclear Information System (INIS)

    Benson, S.W.

    1978-01-01

    A method of separating deuterium, i.e., heavy hydrogen, from certain naturally occurring sources using tuned infrared lasers to selectively decompose specified classes of organic molecules (i.e., RX) into enriched molecular products containing deuterium atoms is described. The deuterium containing molecules are easily separated from the starting material by absorption, distillation or other simple chemical separation techniques and methods. After evaporation such deuterium containing molecules can be burned to form water with an enriched deuterium content or pyrolyzed to form hydrogen gas with an enriched deuterium content. The undecomposed molecules and the other reaction products which are depleted of their deuterium containing species can be catalytically treated, preferably using normal water, to restore the natural abundance of deuterium and such restored molecules can then be recycled

  15. Proposal for implanting a magnetic stable isotope separator

    International Nuclear Information System (INIS)

    Lemos, O.F.

    1988-07-01

    The implantation of an electromagnetic isotope separator able to separate elements of mass from 20 to 250 a.m.u., with an enrichment factor from 10 to 200 times the initial concentration, depending on the elements, is proposed. The most suitable separator type for Brazilian CNEN, considering building installations and minimum conditions for the equipment facilities, the retinue chronogram, the infrastructure, and the personnel training for operation is defined. (M.C.K.) [pt

  16. Gas-centrifuge unit and centrifugal process for isotope separation

    International Nuclear Information System (INIS)

    Stark, T.M.

    1979-01-01

    An invention involving a process and apparatus for isotope-separation applications such as uranium-isotope enrichment is disclosed which employs cascades of gas centrifuges. A preferred apparatus relates to an isotope-enrichment unit which includes a first group of cascades of gas centrifuges and an auxiliary cascade. Each cascade has an input, a light-fraction output, and a heavy-fraction output for separating a gaseous-mixture feed including a compound of a light nuclear isotope and a compound of a heavy nuclear isotope into light and heavy fractions respectively enriched and depleted in the light isotope. The cascades of the first group have at least one enriching stage and at least one stripping stage. The unit further includes means for introducing a gaseous-mixture feedstock into each input of the first group of cascades, means for withdrawing at least a portion of a product fraction from the light-fraction outputs of the first group of cascades, and means for withdrawing at least a portion of a waste fraction from the heavy-fraction outputs of the first group of cascades. The isotope-enrichment unit also includes a means for conveying a gaseous-mixture from a light-fraction output of a first cascade included in the first group to the input of the auxiliary cascade so that at least a portion of a light gaseous-mixture fraction produced by the first group of cascades is further separated into a light and a heavy fraction by the auxiliary cascade. At least a portion of a product fraction is withdrawn from the light fraction output of the auxiliary cascade. If the light-fraction output of the first cascade and the heavy-fraction output of the auxiliary cascade are reciprocal outputs, the concentraton of the light isotope in the heavy fraction produced by the auxiliary cascade essentially equals the concentration of the light isotope in the gaseous-mixture feedstock

  17. Method and apparatus for controlled condensation isotope separation

    International Nuclear Information System (INIS)

    Sullivan, J.A.; Lee, J.T. Jr.; Kim, K.C.

    1981-01-01

    The invention provides a method for producing controlled homogeneous condensation of a molecular feed gas containing several isotopes. The feed gas flows at supersonic rates through an expansion nozzle under conditions at which the gas would normally condense. The gas is irradiated with laser radiation of a wavelength that selectively excites those molecules in the feed gas that contain a particular isotope, thus preventing their condensation. Condensate particles may be aerodynamically separated from the flowing gas stream

  18. Lasers for isotope separation processes and their properties

    International Nuclear Information System (INIS)

    George, E.V.; Krupke, W.F.

    1976-08-01

    The laser system requirements for isotope enrichment are presented in the context of an atomic uranium vapor process. Coherently pumped dye lasers using as the pump laser either the frequency doubled Nd:YAG or copper vapor are seen to be quite promising for meeting the near term requirements of a laser isotope separation (LIS) process. The utility of electrical discharge excitation of the rare gas halogens in an LIS context is discussed

  19. Isotope separation by laser deflection of an atomic beam

    International Nuclear Information System (INIS)

    Bernhardt, A.F.

    1975-02-01

    Separation of isotopes of barium was accomplished by laser deflection of a single isotopic component of an atomic beam. With a tunable narrow linewidth dye laser, small differences in absorption frequency of different barium isotopes on the 6s 2 1 S 0 --6s6p 1 P 1 5536A resonance were exploited to deflect atoms of a single isotopic component of an atomic beam through an angle large enough to physically separate them from the atomic beam. It is shown that the principal limitation on separation efficiency, the fraction of the desired isotopic component which can be separated, is determined by the branching ratio from the excited state into metastable states. The isotopic purity of the separated atoms was measured to be in excess of 0.9, limited only by instrumental uncertainty. To improve the efficiency of separation, a second dye laser was employed to excite atoms which had decayed to the 6s5d metastable state into the 6p5d 1 P 1 state from which they could decay to the ground state and continue to be deflected on the 5535A transition. With the addition of the second laser, separation efficiency of greater than 83 percent was achieved, limited by metastable state accumulation in the 5d 2 1 D 2 state which is accessible from the 6p5d 1 P 1 level. It was found that the decay rate from the 6p5d state into the 5d 2 metastable state was fully 2/3 the decay rate to the ground state, corresponding to an oscillator strength of 0.58. (U.S.)

  20. Wire anode for isotope separation apparatus

    International Nuclear Information System (INIS)

    Janes, G.S.; Dotson, J.P.

    1976-01-01

    In uranium enrichment, an electrode structure of thin, tensioned, parallel wires is claimed for use in applying an electric field to a region of a flowing uranium plasma including selectively ionized particles in order to accelerate the ionized particles for separate collection without interfering with the motion of neutral particles. 24 claims, 3 drawing figures

  1. Isotope separation using molecular gases and molecular lasers

    International Nuclear Information System (INIS)

    Jetter, H.

    1975-01-01

    Isotope separation using molecular gas and molecular lasers offers several advantages over the alternative method which uses dye lasers and atomic vapour. These advantages are the easy handling of the raw material, the big isotopic shift in the IR, the good efficiency of the laser and the chemical extraction of the excited isotopes. In the case of uranium difficulties arise from the great number of superimposed lines in the absorption band of the UF 6 molecule. Several of these absorption bands were measured using laser spectrometers with ultra-high resolution. The conditions for selective excitation were estimated. (orig.) [de

  2. An isotope-enrichment unit and a process for isotope separation

    International Nuclear Information System (INIS)

    1981-01-01

    A process and equipment for isotope enrichment using gas-centrifuge cascades are described. The method is described as applied to the separation of uranium isotopes, using natural-abundance uranium hexafluoride as the gaseous-mixture feedstock. (U.K.)

  3. Study on the Effect of the Separating Unit Optimization on the Economy of Stable Isotope Separation

    Directory of Open Access Journals (Sweden)

    YANG Kun

    2015-01-01

    Full Text Available An economic criterion called as yearly net profit of single separating unit (YNPSSU was presented to evaluate the influence of structure optimization on the economy. Using YNPSSU as a criterion, economic analysis was carried out for the structure optimization of separating unit in the case of separating SiF4 to obtain the 28Si and 29Si isotope. YNPSSU was calculated and compared with that before optimization. The results showed that YNPSSU was increased by 12.3% by the structure optimization. Therefore, the structure optimization could increase the economy of the stable isotope separation effectively.

  4. Method of deuterium isotope separation and enrichment

    International Nuclear Information System (INIS)

    Benson, S.W.

    1979-01-01

    A method is described for separating and enriching deuterium containing molecules comprising the steps of: providing a source of organic molecules containing a normal abundance of deuterium atoms, the organic molecules having a structural formula RX, in which R is an organic radical selected from ethyl, isopropyl, t-butyl and 3-cyclopentenyl, and in which X is selected from F, Cl, Br and OH, and wherein R represents 3-cyclopentenyl, X may additionally represent H; exposing the molecules to the radiation of at least one pulsed infrared laser source which has been specifically tuned and focussed to selectively decompose RX molecules containing deuterium to form an enriched olefin specie containing deuterium, and HX; and separating the deuterium enriched olefin specie from the undecomposed deuterium depleted RX molecules and HX. (author)

  5. Separation of boron isotopes by infrared laser

    International Nuclear Information System (INIS)

    Suzuki, Kazuya

    1995-01-01

    Vibrationally excited chemical reaction of boron tribromide (BBr 3 ) with oxygen (O 2 ) is utilized to separate 10 B and 11 B. Infrared absorption of 10 BBr 3 is at 11.68μ and that of 11 BBr 3 is at 12.18μ. The wavelengths of ammonia laser made in the laboratory were mainly 11.71μ, 12.08μ and 12.26μ. Irradiation was done by focussing the laser with ZnSe lens on the sample gas (mixture of 1.5 torr of natural BBr 3 and 4.5 torr of O 2 ) in the reaction cell. Depletions of 10 BBr 3 and 11 BBr 3 due to chemical reaction of BBr 3 with O 2 was measured with infrared spectrometer. The maximum separation factor β( 10 B/ 11 B) obtained was about 4.5 (author)

  6. Fraction transfer process in on-line comprehensive two-dimensional liquid phase separations

    Czech Academy of Sciences Publication Activity Database

    Česla, P.; Křenková, Jana

    2017-01-01

    Roč. 40, č. 1 (2017), s. 109-123 ISSN 1615-9306 R&D Projects: GA ČR(CZ) GA14-06319S Institutional support: RVO:68081715 Keywords : capillary electrophoresis * comprehensive liquid chromatography * fraction transfer * two-dimensional separations * liquid chromatography Subject RIV: CB - Analytical Chemistry, Separation OBOR OECD: Analytical chemistry Impact factor: 2.557, year: 2016

  7. The Cryo-Thermochromatographic Separator (CTS) A new rapid separation and alpha-detection system for on-line chemical studies of highly volatile osmium and hassium (Z=108) tetroxides

    CERN Document Server

    Kirbach, U W; Gregorich, K E; Lee, D M; Ninov, V; Omtvedt, J P; Patin, J B; Seward, N K; Strellis, D A; Sudowe, R; Türler, A; Wilk, P A; Zielinski, P M; Hoffman, D C; Nitsche, H

    2002-01-01

    The Cryo-Thermochromatographic Separator (CTS) was designed and constructed for rapid, continuous on-line separation and simultaneous detection of highly volatile compounds of short-lived alpha-decaying isotopes of osmium and hassium (Hs, Z=108). A flowing carrier gas containing the volatile species is passed through a channel formed by two facing rows of 32 alpha-particle detectors, cooled to form a temperature gradient extending from 247 K at the channel entrance down to 176 K at the exit. The volatile species adsorb onto the SiO sub 2 -coated detector surfaces at a characteristic deposition temperature and are identified by their observed alpha-decay energies. The CTS was tested on-line with OsO sub 4 prepared from sup 1 sup 6 sup 9 sup - sup 1 sup 7 sup 3 Os isotopes produced in sup 1 sup 1 sup 8 sup , sup 1 sup 2 sup 0 Sn( sup 5 sup 6 Fe, 3,4,5n) reactions. An adsorption enthalpy for OsO sub 4 of -40.2+-1.5 kJ/mol on SiO sub 2 was deduced by comparing the measured deposition distribution with Monte Carlo...

  8. Initial results with the Berkeley on-line mass separator-RAMA

    International Nuclear Information System (INIS)

    Cerny, J.; Moltz, D.M.; Evans, H.C.; Vieira, D.J.; Parry, R.F.; Wouters, J.M.; Gough, R.A.; Zisman, M.S.

    1977-11-01

    Initial performance is described for a reasonably fast and universal (having little or no chemical selectivity) on-line mass analysis system used to expand capabilities in studying nuclei far from stability. The system is termed RAMA, an acronym for Recoil Atom Mass Analyzer. Basically, this system utilizes the helium-jet method to transport activity to a Sidenius hollow-cathode ion source which is coupled to a mass spectrometer. Initial experiments and planned improvements are discussed. Transport efficiencies of between 10 and 60 percent have routinely been achieved, though the latter is much more typical when conditions are optimized

  9. Development of on line automatic separation device for apple and sleeve

    Science.gov (United States)

    Xin, Dengke; Ning, Duo; Wang, Kangle; Han, Yuhang

    2018-04-01

    Based on STM32F407 single chip microcomputer as control core, automatic separation device of fruit sleeve is designed. This design consists of hardware and software. In hardware, it includes mechanical tooth separator and three degree of freedom manipulator, as well as industrial control computer, image data acquisition card, end effector and other structures. The software system is based on Visual C++ development environment, to achieve localization and recognition of fruit sleeve with the technology of image processing and machine vision, drive manipulator of foam net sets of capture, transfer, the designated position task. Test shows: The automatic separation device of the fruit sleeve has the advantages of quick response speed and high separation success rate, and can realize separation of the apple and plastic foam sleeve, and lays the foundation for further studying and realizing the application of the enterprise production line.

  10. On-line separation of iodine species in reactor water using mixer-settlers

    International Nuclear Information System (INIS)

    Malmbeck, R.; Skarnemark, G.

    1995-01-01

    A method for separation of iodine species from water has been developed. It is based on liquid-liquid extraction and separation is achieved in four extraction steps. A system based on this method for continuous separation of iodine species using mixer-settlers has been developed. It consists of four mixer-settler batteries with 4,4,6 and 6 mixer-settler stages each. As organic phase an aliphatic kerosene is used and the separation is improved if the organic solvent has been pretreated with iodine carrier, stripped and washed. With an aqueous feed flowrate of 10 ml/min and mixer-settler battery phase flowratios of approximately 0.1 except for the elementary iodine strip battery with a phase flowratio of 1, the system separation performance is 92% for methyl iodide, 97% for iodate and elementary iodine and 99% for iodide. (orig.)

  11. Electromagnetic separator for light and middle isotope elements

    International Nuclear Information System (INIS)

    Bernas, R.

    1952-01-01

    We describe a separator of isotope with a 60 deg magnetic sector that permits, thanks to a process of neutralization of the space charge, to use efficiently intense ion beams. The ion source for solid is essentially constituted by a discharge of hot cathode in a magnetic field and provides an ion beam focused of more than 10 mA. The result of the first separations (Zn, Sb, Hg) indicates that the isotopes of various elements can be obtained in quantities varying from 10 to 100 mg/24 hours. (author) [fr

  12. Separation of boron isotopes using NMG type anion exchange resin

    International Nuclear Information System (INIS)

    Itagaki, Takaharu; Kosuge, Masao; Fukuda, Junji; Fujii, Yasuhiko.

    1992-01-01

    Ion exchange separation of boron isotopes (B-10 and B-11) has been studied by using a special boron selective ion exchange resin; NMG (n-methyl glucamine)-type anion exchange resin. The resin has shown a large isotope separation coefficient of 1.02 at the experimental conditions of temperature, 80degC, and boric acid concentration, 0.2 M (mole/dm 3 ). Enriched B-10 (92%) was obtained after the migration of 1149 m by a recyclic operation of ion exchange columns in a merry-go-round method. (author)

  13. Use of an isotope separator at the INEL

    International Nuclear Information System (INIS)

    Anderl, R.A.

    1977-01-01

    An electromagnetic isotope separator with a retardation lens as a collector was used to prepare highly enriched samples of Nd-143, -144, -145, -146, -148, -150, Sm-147, -149; Eu-151, -152, -153, -154. The 50 μg to 75 μg samples, deposited on 1 mil nickel foil or 0.5 mil vanadium foil, are part of a sample set to be irradiated in EBR-II as part of an integral-capture cross-section measurement program at the INEL. The isotope separator and the apparatus used for the sample preparation are described

  14. Preliminary review on isotope separation of long life fission products. Application research of laser isotope separation to 135Cs

    International Nuclear Information System (INIS)

    Oshita, Hironori; Ozawa, Masaki; Ishikawa, Makoto; Koyama, Shin'ichi; Akatsuka, Hiroshi

    2007-09-01

    Recently establishment of self consistent nuclear fuel cycle has been required with respect to economical efficiency, safety and reduction of the load to the environment. Especially 135 Cs included in spent fuel of nuclear power plants has extremely long half life (3.0x10 6 y) and its water solubility leads to the anxiety of exudation into ground water for geologic disposal. The conventional methods for isotope separation based on the mass difference of isotope could not gain large separation factors, which leads to the requirement of operational repetition and large equipment. Furthermore many elements of which the masses are near to that of the object isotope are included in spent fuel, which makes it difficult to expect high separation factor by the methods merely based on the mass difference. Recent technology development of laser e.g. dye laser or semi-conductor laser has come to make it possible in principle to excite a specific isotope and separate it from other isotopes making use of its intrinsic physical and chemical properties of the excited state. This laser isotope separation (LIS) technique is believed to be suitable for cesium because of its stable properties on light absorption and emission and many studies have come to be made. This document reviews the principle, application to the separation of 135 Cs and current status of LIS and reports the subjects to be solved and suggestions; especially laser induced chemical reactions expected as a low-cost and simple equipment isotope separation method. The resulting extracted subjects are 1) the specification of the excited states of cesium i.e. extra-nuclear electron configuration, life (or duration) and transition probability, 2) the factors that may effect on the isotope shift of cesium; the mean square radius of the nucleus, electric quadrupole moment and extra nuclear electron wave function at the nucleus, 3) the factors that may cause the disturbance of the selectivity; resonant energy transference

  15. Separation of tritium from other hydrogen isotopes

    International Nuclear Information System (INIS)

    Roth, E.

    1988-01-01

    The paper describes a plant that has been operated at Marcoule for tritium production and used thermal diffusion enrichment, a facility that was built in Saclay to enrich hydrogen in tritium for low level measurements, and the Laue Langevin Institute tritium extraction plant. Details are given on the project under construction for the tritium separation facility at JET using Gas Chromatography, and on proposals for circuits for NET. Studies on catalysers for liquid phase catalytic exchange, on electrolysers, or different gas chromatography arrangements, are described. Systems designed for reprocessing plants, for detritiation of heavy water by distillation are briefly accounted for

  16. Isotopic exchange reactions. Kinetics and efficiency of the reactors using them in isotopic separation

    International Nuclear Information System (INIS)

    Ravoire, Jean

    1979-11-01

    In the first part, some definitions and the thermodynamic and kinetic isotopic effect concepts are recalled. In the second part the kinetic laws are established, in homogeneous and heterogeneous medium (one component being on occasions present in both phases), without and with isotopic effects. Emphasis is put on application to separation of isotopes, the separation factor α being close to 1, one isotope being in large excess with respect to the other one. Isotopic transfer is then given by: J = Ka (x - y/α) where x and y are the (isotopic) mole fractions in both phases, Ka may be either the rate of exchange or a transfer coefficient which can be considered as the 'same in both ways' if α-1 is small compared to the relative error on the measure of Ka. The third part is devoted to isotopic exchange reactors. Relationships between their efficiency and kinetics are established in some simple cases: plug cocurrent flow reactors, perfectly mixed reactors, countercurrent reactors without axial mixing. We treat only cases where α and the up flow to down flow ratio is close to 1 so that Murphee efficiency approximately overall efficiency (discrete stage contactors). HTU (phase 1) approximately HTU (phase 2) approximately HETP (columns). In a fourth part, an expression of the isotopic separative power of reactors is proposed and discussed [fr

  17. Position-specific isotope analysis by on-line pyrolysis coupled to IRMS

    Science.gov (United States)

    Gilbert, A.; Suda, K.; Yamada, K.; Ueno, Y.; Yoshida, N.

    2016-12-01

    Position-specific isotopic analyses (PSIA) provide unique information regarding the sources, sinks and processes related to natural molecules. For instance, PSIA of short-chain hydrocarbons could lead to temperature of formation and maturity of natural gas reservoirs [1][2]. In the last decade, quantitative Nuclear Magnetic Resonance (NMR) specrometry has been used for PSIA of organic molecules such as glucose or n-alkanes [3][4]. However, due to its low sensitivity, application to low amount geochemical samples remains challenging. In 1997, Corso & Brenna proposed to adapt a pyrolysis furnace to an isotope ratio mass spectrometer, making it possible the thermal degradation of the target molecule and the subsequent analysis of the d13C values of the fragments formed [5]. Starting from fatty acid methyl esters they demonstrated the absence of rearrangement during pyrolytic degradation and could determine the d13C value of carboxyl C-atom position. We adapted the system for the full characterization of position-specific isotope composition of small molecules (ethanol, acetic acid, alanine, propane). Nanomole amount of sample can be analyzed with a precision on intramolecular d13C values of 1‰ or lower [2]. We recently analyzed abiotic and thermogenic propane samples both from the field and from lab simulations. PSIA of propane shows systematic differences of position-specific isotope composition between thermogenic and abiotic samples. While the former show 13C-depletion on the terminal C-atom position - consistent with thermal cracking kinetic models [6] - abiotic samples show little or no preference for terminal or central 13C-isotopomer. These results emphasize the potential of PSIA to trace the the processes associated with organic molecules production. [1] Piasecki et al. 2016 GCA 188, 58 [2] Gilbert et al. 2016 GCA 177, 205 [3] Gilbert et al. 2012 PNAS, 109, 18204 [4] Gilbert et al. 2013 Org. Geochem, 62, 56 [5] Corso & Brenna 1997 PNAS, 94, 1049 [6] Tang et

  18. On-line separation of Pu(III) and Am(III) using extraction and ion chromatography

    International Nuclear Information System (INIS)

    Jernstroem, J.; Lehto, J.; Betti, M.

    2007-01-01

    An on-line method developed for separating plutonium and americium was developed. The method is based on the use of HPLC pump with three analytical chromatographic columns. Plutonium is reduced throughout the procedure to trivalent oxidation state, and is recovered in the various separation steps together with americium. Light lanthanides and trivalent actinides are separated with TEVA resin in thiocyanate/formic acid media. Trivalent plutonium and americium are pre-concentrated in a TCC-II cation-exchange column, after which the separation is performed in CS5A ion chromatography column by using two different eluents. Pu(III) is eluted with a dipicolinic acid eluent, and Am(III) with oxalic acid eluent. Radiochemical and chemical purity of the eluted plutonium and americium fractions were ensured with alpha-spectrometry. (author)

  19. Laser isotope separation and proliferation risks

    Energy Technology Data Exchange (ETDEWEB)

    Fuss, Werner

    2015-02-15

    There is an ongoing discussion on the proliferation danger of laser enrichment of uranium by the Silex process. Here this risk is compared to that of other processes, in particular centrifuges. The two methods need a similar size of the plant for a comparable production rate (in separative work units per year) and the time and costs for their construction do not differ much. This conclusion from published material does not depend on technical details of Silex. But enough details are known to allow for additional conclusions: Whereas the selectivity (enrichment factor) in the Silex process seems higher, the energy consumption is probably larger. Due to the laser's repetition rate being insufficient for the molecular beam, the method has probably a low depletion factor; this is a serious disadvantage for cascading for high enrichment such as for bomb uranium, although it may be acceptable for low enrichment without cascading for reactor purposes.

  20. Simulation of startup period of hydrogen isotope separation distillation column

    International Nuclear Information System (INIS)

    Sazonov, A.B.; Kagramanov, Z.G.; Magomedbekov, Eh.P.

    2003-01-01

    Kinetic procedure for the mathematical simulation of start-up regime of rectification columns for molecular hydrogen isotope separation was developed. Nonstationary state (start-up period) of separating column for rectification of multi-component mixture was calculated. Full information on equilibrium and kinetic physicochemical properties of components in separating mixtures was used for the calculations. Profile of concentration of components by height of column in task moment of time was calculated by means of differential equilibriums of nonstationary mass transfer. Calculated results of nonstationary state of column by the 2 m height, 30 mm diameter during separation of the mixture: 5 % protium, 70 % deuterium, 25 % tritium were illustrated [ru

  1. Optimizing design parameter for light isotopes separation by distillation method

    International Nuclear Information System (INIS)

    Ahmadi, M.

    1999-01-01

    More than methods are suggested in the world for producing heavy water, where between them chemical isotopic methods, distillation and electro lys are used widely in industrial scale. To select suitable method for heavy water production in Iran, taking into consideration, domestic technology an facilities, combination of hydrogen sulphide-water dual temperature process (Gs) and distillation (D W) may be proposed. Natural water, is firstly enriched up to 15 a% by G S process and then by distillation unit is enriched up to the grade necessary for Candu type reactors (99.8 a%). The aim of present thesis, is to achieve know-how, optimization of design parameters, and executing basic design for water isotopes separation using distillation process in a plant having minimum scale possible. In distillation, vapour phase resulted from liquid phase heating, is evidently composed of the same constituents as liquid phase. In isotopic distillation, the difference in composition of constituents is not considerable. In fact alteration of constituents composition is so small that makes the separation process impossible, however, direct separation and production of pure products without further processing which becomes possible by distillation, makes this process as one of the most important separation processes. Profiting distillation process to produce heavy water is based on difference existing between boiling point of heavy and light water. The trends of boiling points differences (heavy and light water) is adversely dependant with pressure. As the whole system pressure decreases, difference in boiling points increases. On the other hand according to the definition, separation factor is equal to the ratio of pure light water vapour pressure to that of heavy water, or we can say that the trend of whole system pressure decrease results in separation factor increase, which accordingly separation factor equation to pressure variable should be computed firstly. According to the

  2. Pulsed CO laser for isotope separation of uranium

    Energy Technology Data Exchange (ETDEWEB)

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

    2012-07-30

    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.

  3. Novel wave/ion beam interaction approach to isotope separation

    International Nuclear Information System (INIS)

    Post, R.F.; Lowder, R.S.; Schwager, L.A.; Barr, W.L.; Warner, B.E.

    1993-02-01

    Numerical simulations and experimental studies have been made related to the possibility of employing an externally imposed electrostatic potential wave to separate isotopes. This wave/ion interaction is a sensitive function of the wave/ion difference velocity and for the appropriate wave amplitude and wave speed, a lighter faster isotope will be reflected by the wave to a higher energy while leaving heavier, slower isotopes virtually undisturbed in energy -- allowing subsequent ion separation by simple energy discrimination. In these experiments, a set of some 200 individual, electrodes, which surrounded a microamp beam of neon ions, was used to generate the wave. Measurements of the wave amplitudes needed for ion reflection and measurements of the final energies of those reflected ions are consistent with values expected from simple kinetic arguments and with the more detailed results of numeric simulations

  4. Bibliographical study on photochemical separation of uranium isotopes

    International Nuclear Information System (INIS)

    Bougon, Roland

    1975-01-01

    The objective of this report is to propose an overview of knowledge and current works on isotopic separation of uranium by means of selective excitation where this excitation is obtained by a light source with a wave length corresponding to a selective or preferential absorption by a molecule or by the atom itself of one of the isotopes. After a brief overview of principles and requirements of isotopic separation by selective excitation, the author reviews compounds which can be used for this process. These compounds are mainly considered in terms of spectroscopy, and the study focuses on the most volatile among them, the uranium hexafluoride, its spectra, and possible processes for extraction. Some much less volatile uranium compounds are also mentioned with, when available, their spectroscopic properties. The uranium vapour excitation process is described, and some orientations for further researches are proposed [fr

  5. Separation of hydrogen isotopes for tritium waste removal

    International Nuclear Information System (INIS)

    Wilkes, W.R.

    1975-01-01

    A distillation cascade for separating hydrogen isotopes was simulated by means of a multicomponent, multistage computer code. A hypothetical test mixture containing equal atomic fractions of protium, deuterium and tritium, equilibrated to high temperature molecular concentrations was used as feed. The results show that a two-column cascade can be used to separate the protium from the tritium. Deuterium appears both in the protium and the tritium product streams. (auth)

  6. Preparation of calcium-separated isotope targets using small samples

    International Nuclear Information System (INIS)

    Thomas, G.E.

    1975-01-01

    Targets are routinely evaporated using a few milligram quantities of separated isotopes of calcium with reducing agents. The source to target distance is 3.0 cm with the substrate, if necessary, as thin as 15 μg/cm 2 carbon or 100 μg/cm 2 of gold. A tantalum closed boat, heat shield, and special collimator system are used

  7. The design of an isotope separation system for JET

    International Nuclear Information System (INIS)

    Sherman, R.H.

    1987-10-01

    Cryogenic distillation is planned as one of the processes to be used for isotope separation at JET. Three possible configurations of columns for this service are presented and discussed. The ability to easily control a system of columns must weigh heavily in the final selection of a process for construction. 5 refs., 6 figs., 6 tabs

  8. Control strategies for laser separation of carbon isotopes

    Indian Academy of Sciences (India)

    Laser isotope separation (LIS) by infrared laser chemistry of polyatomic molecules has come a long way since its discovery. The last decade has seen considerable efforts in scaling up of the process for light elements like carbon, oxygen and silicon. These efforts aim at ways to improve both the enrichment factor and the ...

  9. Control strategies for laser separation of carbon isotopes

    Indian Academy of Sciences (India)

    Unknown

    Control strategies for laser separation of carbon isotopes. V PARTHASARATHY*, A K ... The emerging market for medical applications of C-13 is projected to be in the range of hundreds of ..... thermal effects during irradiation. In the absence of ...

  10. Modelling of multifrequency IRMPD for laser isotope separation

    Indian Academy of Sciences (India)

    Unknown

    This model was exploited in analysing our MPD results ... separation method for 235U, the fissile isotope of uranium needed to fuel light water ... for analysis. The radio-GC consisted of a commercial GC (Shimadzu GC-R1A) equipped with thermal conductivity detector (TCD) and an indigenously built proportional counter.

  11. The design of a switchyard for the NSF isotope separator

    International Nuclear Information System (INIS)

    Malcolm, I.C.; Grant, I.S.

    1982-01-01

    In examining design requirements for the optics of the NSF isotope separator, first-order considerations, voltage requirements, second-order considerations, and shim coil design are discussed. The results are given of a computer study of the system comprising of quadrupole triplet, magnetic and electrostatic sectors. The effects of the accuracy in the fabrication of the electrostatic sector are considered. (U.K.)

  12. New on-line method for water isotope analysis of speleothem fluid inclusions using laser absorption spectroscopy (WS-CRDS)

    Science.gov (United States)

    Affolter, S.; Fleitmann, D.; Leuenberger, M.

    2014-01-01

    A new online method to analyse water isotopes of speleothem fluid inclusions using a wavelength scanned cavity ring down spectroscopy (WS-CRDS) instrument is presented. This novel technique allows us to simultaneously measure hydrogen and oxygen isotopes for a released aliquot of water. To do so, we designed a new simple line that allows the on-line water extraction and isotope analysis of speleothem samples. The specificity of the method lies in the fact that fluid inclusions release is made on a standard water background, which mainly improves the δD reliability. To saturate the line, a peristaltic pump continuously injects standard water into the line that is permanently heated to 140 °C and flushed with dry nitrogen gas. This permits instantaneous and complete vaporisation of the standard water resulting in an artificial water background with well-known δD and δ18O values. The speleothem sample is placed into a copper tube, attached to the line and after system stabilisation is crushed using a simple hydraulic device to liberate speleothem fluid inclusions water. The released water is carried by the nitrogen/standard water gas stream directly to a Picarro L1102-i for isotope determination. To test the accuracy and reproducibility of the line and to measure standard water during speleothem measurements a syringe injection unit was added to the line. Peak evaluation is done similarly as in gas chromatography to obtain δD and δ18O isotopic composition of measured water aliquots. Precision is better than 1.5‰ for δD and 0.4‰ for δ18O for water measurement for an extended range (-210 to 0‰ for δD and -27 to 0‰ for δ18O) primarily dependent on the amount of water released from speleothem fluid inclusions and secondarily on the isotopic composition of the sample. The results show that WS-CRDS technology is suitable for speleothem fluid inclusion measurements and gives results that are comparable to Isotope Ratio Mass Spectrometry (IRMS) technique.

  13. Spectroscopic and physicochemical measurements for on-line monitoring of used nuclear fuel separation processes

    Energy Technology Data Exchange (ETDEWEB)

    Nee, Ko; Nilsson, M. [Department of Chemical Engineering and Material Science, University of California, 916 Engineering Tower, Irvine, CA 92697-2575 (United States); Bryan, S.; Levitskaia, T. [Pacific Northwest National Laboratory, PO BOX 999, Richland, CA 99352 (United States)

    2013-07-01

    Separation processes for used nuclear fuel are often complicated and challenging due to the high constraints in purity of the products and safeguards of the process streams. In order to achieve a safe, secure and efficient separation process, the liquid streams in the separation process require close monitoring. Due to the high radiation environment, sampling of the materials is difficult. Availability of a detection technique that is remote, non-destructive and can avoid time-delay caused by retrieving samples would be beneficial and could minimize the exposure to personnel and provide material accountancy to avoid diversion (non-proliferation). For example, Ultra Violet (UV), Visible (Vis), Near-Infrared (NIR) and Raman spectroscopy that detect and quantify elements present in used nuclear fuel, e.g. lanthanides, actinides and molecules such as nitrate, can be used. In this work, we have carried out NIR and Raman spectroscopy to study aqueous solutions composed of different concentrations of nitric acid, sodium nitrate, and neodymium at varied temperatures. A chemometric model for online monitoring based on the PLS-Toolbox (MATLAB) software has been developed and validated to provide chemical composition of process streams based on spectroscopic data. In conclusion, both of our NIR and Raman spectra were useful for H{sup +} and NO{sub 3} prediction, and only NIR was helpful for the Nd{sup 3+} prediction.

  14. The on-line mass separator SIRIUS at the Strasbourg Reactor

    International Nuclear Information System (INIS)

    Zirnheld, J.P.; Schutz, L.

    1979-01-01

    The SIRIUS facility was developed to isolate short-lived neutron-rich nuclides far from the line of β stability. The installation, which consists of a helium-jet fission-product transport system, an ion source, an accelerator and a deviation magnet, is described. The main characteristics of the whole system can be summarized as: (1) the fission-product transmission to the ion source is about 90%: (2) the mass resolving power is of the order of 500: (3) the total transit time between production and detection is less than 1s : (4) the overall efficiency of the system is on the average better than 5x10 -5 . The nuclei available for nuclear spectroscopic studies have been examined. With a neutron flux of 5x10 11 /cm 2 .s and 730 mg for the uranium target, about 50 neutron-rich rare-earth isotopes (many of which had previously been unavailable) are available with sufficient activities for nuclear spectroscopic studies. (Auth.)

  15. MINLP solution for an optimal isotope separation system

    International Nuclear Information System (INIS)

    Boisset-Baticle, L.; Latge, C.; Joulia, X.

    1994-01-01

    This paper deals with designing of cryogenic distillation systems for the separation of hydrogen isotopes in a thermonuclear fusion process. The design must minimize the tritium inventory in the distillation columns and satisfy the separation requirements. This induces the optimization of both the structure and the operating conditions of the columns. Such a problem is solved by use of a Mixed-Integer NonLinear Programming (MINLP) tool coupled to a process simulator. The MINLP procedure is based on the iterative and alternative treatment of two subproblems: a NLP problem which is solved by a reduced-gradient method, and a MILP problem, solved with a Branch and Bound method coupled to a simplexe. The formulation of the problem and the choice of an appropriate superstructure are here detailed, and results are finally presented, concerning the optimal design of a specific isotope separation system. (author)

  16. Tandem on-line continuous separations for atomic spectroscopic indirect analysis: iodide determination by ICP-AES

    International Nuclear Information System (INIS)

    Garcia, A.M.; Sanchez Uria, J.E.; Sanz-Medel, A.; Quintero Ortega, M.C.; Bautista, J.C.

    1992-01-01

    A sensitive and selective indirect determination of iodide by inductively coupled plasma emission spectrometry (ICP-AES) based on the principle of tandem on-line continuous separations as an alternative means of introducing samples into plasmas is proposed. Iodide is continuously extracted as an ion-pair into xylene by mixing the sample with Hg(II) and dipyridil solutions. The organic phase (containing the analyte in [Hg(Dipy) 2 ]I 2 form) is on-line continuously mixed with NaBH 4 (in DMF) and acetic acid solutions. Mercury vapour continuously generated from this organic phase is separated in a classical U-type gas-liquid separation device. The system has been optimized for the continuous extraction of KI, for the direct generation of cold mercury vapour from xylene and for the final ICP-AES determination of mercury. The optimised method has been applied to the determination of iodide (detection limit 20 ng/ml of iodide) in table salt and in synthetic samples. Very good agreement between found and certified results was observed. The usefulness and convenience of such alternative sample chemical pretreatment/presentation to the ICP is thus demonstrated for indirect determinations to be carried out by atomic spectroscopy methods. (authors)

  17. Proposed configuration for ITER hydrogen isotope separation system (ISS)

    International Nuclear Information System (INIS)

    Lazar, A.; Brad, S.; Sofalca, N.; Vijulie, M.; Cristescu, I.; Doer, L; Wurster, W.

    2008-01-01

    Full text: The isotope separation system utilizes cryogenic distillation and catalytic reaction for isotope exchange to separate elemental hydrogen isotope gas mixtures. The ISS shall separate hydrogen isotope mixtures from two sources to produce up to five different products. These are: protium, effluent for discharge to the atmosphere, deuterium for fuelling, deuterium for NB injector (NBI) source gas, 50 % and 90% T fuelling streams. The concept of equipment 3D layout for the ISS main components were developed using the Part Design, Assembly Design, Piping Design, Equipment Arrangement and Plant Layout application from CATIA V5. The 3D conceptual layouts for ISS system were created having as reference the DDD -32-B report, the drawings 0028.0001.2D. 0100. R 'Process Flow Diagram'; 0029.0001.2D. 0200.R 'Process Instrumentation Diagram -1' (in the cold box); 0030.0001.2D. 0100. R 'Process Instrumentation Diagram -2' (in the hard shell confinement) and imputes from TLK team. The main components designed for ISS are: ISS cold box system (CB) with cryogenic distillation columns (CD) and recovery heat exchangers (HX), ISS hard shell containment (HSC) system with metals bellow pumps (MB) and chemical equilibrators (RC), valve box system, instrumentation box system, vacuum system and hydrogen expansion vessels. Work related to these topics belongs to the contract FU06-CT-2006-00508 (EFDA 06-1511) from the EFDA Technology Workprogramm 2006 and was done in collaboration with FZK Association team during the period January 2007 - September 2008. (authors)

  18. Concentration control in an isotope separation plant; Regulation des concentrations dans une usine de separation isotopique

    Energy Technology Data Exchange (ETDEWEB)

    Jacques, R [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1962-07-01

    Concentration control is examined for the case of a gaseous diffusion plant for uranium isotope separation. The effects of various typical perturbations are described and adequate systems of corrective actions are determined according to selected criteria. (author) [French] On considere une installation de separation des isotopes de l'uranium par diffusion gazeuse. On etudie les effets sur les concentrations isotopiques de diverses perturbations type donnees a l'avance et on determine le systeme d'actions correctives qui permet de reduire ces effets d'apres un critere d'efficacite donne. (auteur)

  19. An on-line mass-separator for thermically ionisable fission products: OSTIS

    International Nuclear Information System (INIS)

    Wuensch, K.-D.

    1978-01-01

    A mass separator has been designed and built for the installed at an external neutron guide tube (flux approximately 10 9 nsub(th)/s cm 2 ) of the High Flux Reactor of the Institute Laue-Langevin in Grenoble. The ion source consists of a high temperature oven containing fissile target material (approximately 2 g 235 U) embedded in porous carbon. Fission products formed in the target are thermalised in the carbon where only the alkali fission products diffuse quickly to the extraction hole. There only Rb and Cs are thermally ionized. Accelerated to 20 kV, these ions pass through a deflecting magnetic field (rhosub(m) approximately 215 mm, rho=77.5 0 ) for mass analysis and an electrostatic quadrupole to form a 5 mm diameter spot about 1 m outside the concrete shielding. Intensities of some 10 6 atoms per second were reached. The system allows all types of nuclear spectroscopy of Rb, Cs and their β-decay chain daughters as well as the measurement of yields and fission neutrons. It has been in nearly continuous operation for more than two years in Grenoble and first results are reported. (Auth.)

  20. The separation nozzle process for uranium isotope enrichment

    International Nuclear Information System (INIS)

    Becker, E.W.

    1977-01-01

    In the separation nozzle process, uranium isotope separation is brought about by the mass dependence of the centrifugal forces in a curved flow of a UF 6 /H 2 -mixture. Due to the large excess in hydrogen the high ration of UF 6 flow velocity to thermal velocity required for an effective isotope separation is obtained at relatively low expansion ratios and, accordingly, with relatively low gas-dynamic losses. As the optimum Reynolds number of the curved jet is comparatively low and a high absolute pressure is essential for economic reasons, the characteristic dimensions of the nozzle systems are made as small as possible. For commercial application in the near future systems involving mechanical jet deflection were developed. However, promising results were also obtained with separation nozzle systems generating a streamline curvature by the interaction of opposed jets. Most of the development work has been done at the Nuclear Research Center of Karlsruhe. Since 1970 the German company STEAG has been involved in the commercial implementation of the process. Two industrial-scale separative stages were tested successfully. This work constitutes the basis of planning of a separation nozzle demonstration plant to be built in Brazil

  1. Alternative applications of atomic vapor laser isotope separation technology

    International Nuclear Information System (INIS)

    1991-01-01

    This report was commissioned by the Secretary of Energy. It summarizes the main features of atomic vapor laser isotope separation (AVLIS) technology and subsystems; evaluates applications, beyond those of uranium enrichment, suggested by Lawrence Livermore National Laboratory (LLNL) and a wide range of US industries and individuals; recommends further work on several applications; recommends the provision of facilities for evaluating potential new applications; and recommends the full involvement of end users from the very beginning in the development of any application. Specifically excluded from this report is an evaluation of the main AVLIS missions, uranium enrichment and purification of plutonium for weapons. In evaluating many of the alternative applications, it became clear that industry should play a greater and earlier role in the definition and development of technologies with the Department of Energy (DOE) if the nation is to derive significant commercial benefit. Applications of AVLIS to the separation of alternate (nonuranium) isotopes were considered. The use of 157 Gd as burnable poison in the nuclear fuel cycle, the use 12 C for isotopically pure diamond, and the use of plutonium isotopes for several nonweapons applications are examples of commercially useful products that might be produced at a cost less than the product value. Separations of other isotopes such as the elemental constituents of semiconductors were suggested; it is recommended that proposed applications be tested by using existing supplies to establish their value before more efficient enrichment processes are developed. Some applications are clear, but their production costs are too high, the window of opportunity in the market has passed, or societal constraints (e.g., on reprocessing of reactor fuel) discourage implementation

  2. On-line hyperfine structure and isotope shift measurements with diffuse light collection and photon burst detection

    International Nuclear Information System (INIS)

    Lassen, J.; Benck, E.C.; Schuessler, H.A.

    1997-01-01

    An experiment is presently being set up which combines collinear-fast-beam laser spectroscopy with photon burst spectroscopy. Selectivity is provided by the large kinetic isotope shifts together with the practically Doppler free linewidth of the fluorescence from the fast atom beam. The photon burst detection, based on photon correlations in the resonance fluorescence, increases the sensitivity, so that on-line optical isotope shift and hyperfine structure measurements on low intensity radioactive beams become feasible. In order to improve photon burst detection the solid angle of detection and the observation time have to be optimized. To this end a diffuse reflecting cavity has been designed and built, which collects fluorescence over a 45 cm length of the beam and covers the full solid angle. The light collection efficiency of the cavity is calculated to be about 45%. The cavity is being tested with a 11 keV beam of krypton atoms, probing the near infrared transitions in our apparatus at Texas A ampersand M University. copyright 1997 American Institute of Physics

  3. Deuterium isotope separation factor between hydrogen and liquid water

    International Nuclear Information System (INIS)

    Rolston, J.H.; den Hartog, J.; Butler, J.P.

    1976-01-01

    The overall deuterium isotope separation factor between hydrogen and liquid water, α, has been measured directly for the first time between 280 and 370 0 K. The data are in good agreement with values of α calculated from literature data on the equilibrium constant for isotopic exchange between hydrogen and water vapor, K 1 , and the liquid-vapor separation factor, α/sub V/. The temperature dependence of α over the range 273-473 0 K based upon these new experimental results and existing literature data is given by the equation ln α = -0.2143 + (368.9/T) + (27,870/T 2 ). Measurements on α/sub V/ given in the literature have been surveyed and the results are summarized over the same temperature range by the equation ln α/sub V/ = 0.0592 - (80.3/T) +

  4. Development of Halide and Oxy-Halides for Isotopic Separations

    Energy Technology Data Exchange (ETDEWEB)

    Martin, Leigh R. [Idaho National Lab. (INL), Idaho Falls, ID (United States); Johnson, Aaron T. [Idaho National Lab. (INL), Idaho Falls, ID (United States); Pfeiffer, Jana [Idaho National Lab. (INL), Idaho Falls, ID (United States); Finck, Martha R. [Idaho National Lab. (INL), Idaho Falls, ID (United States)

    2014-10-01

    The goal of this project was to synthesize a volatile form of Np for introduction into mass spectrometers at INL. Volatile solids of the 5f elements are typically those of the halides (e.g. UF6), however fluorine is highly corrosive to the sensitive internal components of the mass separator, and the other volatile halides exist as several different stable isotopes in nature. However, iodide is both mono-isotopic and volatile, and as such presents an avenue for creation of a form of Np suitable for introduction into the mass separator. To accomplish this goal, the technical work in the project sought to establish a novel synthetic route for the conversion NpO2+ (dissolved in nitric acid) to NpI3 and NpI4.

  5. An overview of copper-laser development for isotope separation

    International Nuclear Information System (INIS)

    Warner, B.E.

    1987-01-01

    We have developed a copper-laser pumped dye-laser system that addresses all of the requirements for atomic vapor laser isotope separation. The requirement for high average power for the laser system has led to the development of copper-laser chains with injection-locked oscillators and multihundred-watt amplifiers. By continuously operating the Laser Demonstration Facility, we gain valuable data for further upgrade and optimization

  6. Development laser light facility for uranium isotope separation

    International Nuclear Information System (INIS)

    Dickinson, G.J.

    1992-01-01

    A laser light facility has been built and successfully commissioned as part of a programme to explore the economic potential of Laser Isotope Separation of Uranium. The laser systems are comprised of tunable dye lasers pumped by copper vapour lasers. The requirements for optical beam stability, alignment of lasers in chains, and protection of optical coatings have made challenging demands on the engineering design and operation of the facility. (Author)

  7. Aerodynamic effects in isotope separation by gaseous diffusion

    International Nuclear Information System (INIS)

    Bert, L.A.; Prosperetti, A.; Fiocchi, R.

    1978-01-01

    The turbulent flow of an isotopic mixture in a porous-walled pipe is considered in the presence of suction through the wall. A simple model is formulated for the evaluation of aerodynamic effects on the separation efficiency. The predictions of the model are found to compare very favourably with experiment. In the limit of small suction velocities, results obtained by other investigators for diffusion in a turbulent steam are recovered. (author)

  8. Seismic design criteria for special isotope separation plant structures

    International Nuclear Information System (INIS)

    Wrona, M.W.; Wuthrich, S.J.; Rose, D.L.; Starkey, J.

    1989-01-01

    This paper describes the seismic criteria for the design of the Special Isotope Separation (SIS) production plant. These criteria are derived from the applicable Department of Energy (DOE) orders, references and proposed standards. The SIS processing plant consistent of Load Center Building (LCB), Dye Pump Building (DPB), Laser Support Building (LSB) and Plutonium Processing Building (PPB). The facility-use category for each of the SIS building structures is identified and the applicable seismic design criteria and parameters are selected

  9. Uranium isotope separation from 1941 to the present

    International Nuclear Information System (INIS)

    Maier-Komor, Peter

    2010-01-01

    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 239 Pu was included into the atomic bomb program. 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.

  10. 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.

  11. 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.

  12. On separation of heavy isotopes by means of selective ICRH

    International Nuclear Information System (INIS)

    Kotelnikov, I.A.; Kuzmin, S.G.; Volosov, V.I.

    1998-01-01

    The authors present a theoretical study of the isotope separation by means of isotopically selective ion cyclotron resonance plasma heating (ICRH). The special attention is devoted to the separation of gadolinium isotopes. The ions are supposed to pass through the device shown on Fig. 1 where they are heated by the full-turn-loop antenna that excites RF field with azimuthal number m = 0. They calculate the distribution function of ions in a plasma stream at the orifice of the device. A satisfactory separation is achieved for the following values of parameters. The length of heating zone ell = 200 cm, initial temperature of plasma stream T parallel = 5 eV, T perpendicular = 60 eV, the plasma radius a = 10 cm, plasma density n = 10 12 cm -3 , external magnetic field B = 30 kGs. The energy of resonance ions W = 100 divided-by 200 eV. The latter value is achieved if a current in the antenna loops is equal to 60A with full number of loops N = 150. With the specified parameters, the current in the plasma stream is equal to 15 divided-by 20A. Then the production rate equals to 100 kg of Gd 157 per year. Energy of Gd's ions after pass through the heating zone vs. their axial velocity

  13. Lacan - a global simulation code for laser isotope separation

    International Nuclear Information System (INIS)

    Goldstein, S.; Quaegebeur, J.P.

    1990-01-01

    Dimensioning a Laser Isotope Separation (LIS) plant means calculating the values of a large number of parameters in order to optimize some objective function. In such algorithms the calculation of the objective function must be repeated thousands of times, therefore each elementary calculation must consume little time. LACAN uses simple models to describe the elementary physical processes: evaporation, vapour expansion, interaction between photons and atoms, ion extraction etc ... These simple models are derived from refined modeling codes or are empirical. As an example the optimization of the separative work of an uranium facility is discussed

  14. Method of deuterium isotope separation using ethylene and ethylene dichloride

    International Nuclear Information System (INIS)

    Benson, S.W.

    1982-01-01

    Compounds enriched in deuterium may be obtained from ethylene, vinyl chloride, 1,2-dichloroethane, or propylene by laser isotope separation. Normal molecules of these organic compounds are exposed to infrared laser radiation of a suitable wavelength. Substantially all of the deuterium-containing molecules exposed to the laser can be selectively dissociated and the deuterium-containing products separated from the starting material and other reaction products. The deuterium-containing molecules can be burned to form water with an enriched deuterium content, or pyrolized to form hydrogen gas enriched in deuterium

  15. Isotope separation by chemical exchange process: Final technical report

    International Nuclear Information System (INIS)

    Schneider, A.

    1987-02-01

    The feasibility of a chemical exchange method for the separation of the isotopes of europium was demonstrated in the system EuCl 2 -EuCl 3 . The single stage separation factor, α, in this system is 1.001 or 1.0005 per mass unit. This value of α is comparable to the separation factors reported for the U 4+ - U 6 and U 3+ - Y 4+ systems. The separation of the ionic species was done by precipitation of the Eu 2+ ions or by extraction of the Eu 3+ ions with HDEHP. Conceptual schemes were developed for a countercurrent reflux cascades consisting of solvent extraction contractors. A regenerative electrocel, combining simultaneous europium reduction, europium oxidation with energy generation, and europium stripping from the organic phase is described. 32 refs., 22 figs., 6 tabs

  16. First spatial isotopic separation of relativistic uranium projectile fragments

    International Nuclear Information System (INIS)

    Magel, A.; Voss, B.; Armbruster, P.; Aumann, T.; Clerc, H.G.; Czajkowski, S.; Folger, H.; Grewe, A.; Hanelt, E.; Heinz, A.; Irnich, H.; Jong, M. de; Junghans, A.; Nickel, F.; Pfuetzner, M.; Roehl, C.; Scheidenberger, C.; Schmidt, K.H.; Schwab, W.; Steinhaeuser, S.; Suemmerer, K.; Trinder, W.; Wollnik, H.

    1994-07-01

    Spatial isotopic separation of relativistic uranium projectile fragments has been achieved for the first time. The fragments were produced in peripheral nuclear collisions and spatially separated in-flight with the fragment separator FRS at GSI. A two-fold magnetic-rigidity analysis was applied exploiting the atomic energy loss in specially shaped matter placed in the dispersive central focal plane. Systematic investigations with relativistic projectiles ranging from oxygen up to uranium demonstrate that the FRS is a universal and powerful facility for the production and in-flight separation of monoisotopic, exotic secondary beams of all elements up to Z=92. This achievement has opened a new area in heavy-ion research and applications. (orig.)

  17. Separation of lithium isotopes on ion exchangers; Separation des isotopes du lithium sur echangeurs d'ions

    Energy Technology Data Exchange (ETDEWEB)

    Menes, F; Saito, E; Roth, E [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1958-07-01

    A survey of the literature shows that little information has been published on the separation of lithium isotopes with ion exchange resins. We have undertaken a series of elutions using the ion-exchange resins 'Dowex 50 x 12' and IRC 50, and various eluting solutions. Formulae derived from the treatment of Mayer and Tompkins permit the calculation of the separation factor per theoretical plate. For the solutions tried out in our experiments the separation factors lie in the interval 1.001 to 1.002. These values are quite low in comparison to the factor 1.022 found by Taylor and Urey for ion exchange with zeolites. (author) [French] Nous avons trouve relativement peu de donnees dans la litterature scientifique sur la separation des isotopes de lithium par les resines echangeuses d'ions. Nous avons effectue un certain nombre d'essais sur Dowex 50 X 12 et IRC 50 utilisant divers eluants. Des formules derivees de celles de Mayer et Tompkins permettent le calcul du coefficient de separation par plateau theorique. Pour les eluants etudies, ces facteurs de separation se trouvent entre 1,001 et 1,002. Ces valeurs sont faibles en comparaison du facteur 1,022 trouve par Taylor et Urey pour les zeolithes. (auteur)

  18. Production of high-purity isotopes by electromagnetic separation; Production electromagnetique d'isotope tres purs

    Energy Technology Data Exchange (ETDEWEB)

    Cassignol, Ch [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1958-07-01

    Improvement in isotopic purity of nuclides prepared by electromagnetic separation is searched into the principle of cascades of monochromators. The principal drawback of which is to allow the separation of only one isotope at a time. The electromagnetic separator of Saclay is equipped with an electrostatic post-analyzer, which is described. Significant results are obtained, concerning isotopic enhancements of uranium-235 and mercury-204. A schema of isotopic contagion is then proposed, the basis of it is the scattering of the primary ions in the residual atmosphere of the separator chamber. The most frequent type of collisions being accompanied by neutralisation of the ions, the schema explains the efficiency of the second stage. As a matter of conclusion, some particularities concerning the routine work at a high enhancement, small output machine, are given. (author) [French] L'accroissement de la purete isotopique des especes nucleaires preparees par separation electromagnetique est recherche dans l'emploi du principe des cascades de monochromateurs, moyennant la servitude de ne collecter qu'un isotope a la fois. Le separateur electromagnetique de Saclay est equipe dans ce but d'un post-analyseur electrostatique, qui est decrit. Des resultats significatifs sont donnes, portant sur les enrichissements obtenus dans les separations d'uranium-235 et de mercure-204. Un schema de contagion isotopique est propose. Il est fonde sur la diffusion a petit angle accompagnant la neutralisation des faisceaux primaires par collision avec le gaz residuel. Ce schema permet d'expliquer l'efficacite de l'etage electrostatique. En matiere de conclusion, la methode d'exploitation d'une machine a faible debit et a haut enrichissement est donnee. (auteur)

  19. Isotope separation of 22Na and 24Na with using light induced drift effect

    International Nuclear Information System (INIS)

    Hradecny, C.; Tethal, T.; Ermolaev, I.M.; Zemlyanoj, S.G.; Zuzaan, P.

    1993-01-01

    The LIDIS (Light Drift Isotope Separation) separator without a gas flow is discussed. It is shown, that atomization degree of the separated isotopes limited real separation coefficient. The better buffer gas purification allowed to increase the experimental separation factor of 22 Na and 24 Na isotopes up to 25. The new experimental set up allow to increase the separation efficiency up to 50%. 12 refs.; 5 figs

  20. Hydrogen isotope separation experience at the Savannah River Site

    International Nuclear Information System (INIS)

    Lee, M.W.

    1993-01-01

    Savannah River Site (SRS) is a sole producer of tritium for US Weapons Program. SRS has built Facilities, developed the tritium handling processes, and operated safely for the last forty years. Tritium is extracted from the irradiated reactor target, purified, mixed with deuterium, and loaded to the booster gas bottle in the weapon system for limited lifetime. Tritium is recovered from the retired bottle and recycled. Newly produced tritium is branded into the recycled tritium. One of the key process is the hydrogen isotope separation that tritium is separated from deuterium and protium. Several processes have been used for the hydrogen isotope separation at SRS: Thermal Diffusion Column (TD), Batch Cryogenic Still (CS), and Batch Chromatography called Fractional Sorption (FS). TD and CS requires straight vertical columns. The overall system separation factor depends on the length of the column. These are three story building high and difficult to put in glove box. FS is a batch process and slow operation. An improved continuous chromatographic process called Thermal Cycling Absorption Process (TCAP) has been developed. It is small enough to be about to put in a glove box yet high capacity comparable to CS. The SRS tritium purification processes can be directly applicable to the Fusion Fuel Cycle System of the fusion reactor

  1. Method of concentrating and separating lithium isotopes by laser

    International Nuclear Information System (INIS)

    Yamashita, Mikio; Kashiwagi, Hiroshi.

    1976-01-01

    Purpose: To eliminate the need for repeating separating operation in many stages and permit concentrated lithium of high purity to be obtained in a short period of time. Constitution: Lithium atom vapor is irradiated by a laser of wavelengths resonant to 6 Li or 7 Li absorption spectra present in the neighborhood of 6,707.84 A or 3,232.61 A (chromatic laser being used for oscillation in the neighborhood of 6,707.84 A and ultraviolet laser used for oscillation in the neighborhood of 6,707.84 A) for selectively exciting 6 Li or 7 Li alone. Then, ionization is brought about by using other types of lasers (ultraviolet Ar ion laser being used as the former wavelength laser and visible Ar ion laser as the latter wavelength laser), and only the ionized isotopes are passed through a mass filter and collected by an ion collector, thereby effecting separation of the ionized isotopes from the non-ionized neutral isotopes and their concentration. (Aizawa, K.)

  2. The present state of laser isotope separation of uranium

    International Nuclear Information System (INIS)

    Tashiro, Hideo; Nemoto, Koshichi.

    1994-01-01

    As the methods of uranium enrichment, gas diffusion method and centrifugal separation method in which power consumption is less and the cost is low have been carried out. On the other hand, as the future technology, the research and development of laser isotope separation technology have been carried out. There are the atomic laser separation process in which the laser beam of visible light is irradiated to atomic state uranium and the molecular laser separation process in which far infrared laser beam is irradiated to uranium hexafluoride molecules. The atomic process is divided into three steps, that is, the processes of uranium evaporation, the reaction of uranium with laser beam and the recovery of enriched uranium. The principle of the laser separation is explained. The state of development of laser equipment and separation equipment is reported. The principle and the present state of development of the molecular separation process which consists of the cooling of UF 6 gas, the generation of high power 16 μm laser pulses and the collection of the reaction product are explained. The present state of both processes in foreign countries is reported. (K.I.)

  3. The physics of uranium isotope separation by laser

    International Nuclear Information System (INIS)

    Clerc, M.; Rigny, P.

    1985-01-01

    SILMO is the isotopic separation process using a laser and the uranium hexafluoride molecule. SILVA is the laser process whereby the enriched medium is formed by the atomic vapour from uranium. The scientific bases of the two processes are described using very simple parameters such as photoionisation selectivity and useful availability of photons and atoms. It is shown that SILVA can have a specific energy consumption lower than 100 KWh/UTS. A separator module could be made up, for instance, of a dihedron of uranium vapour several metres long in which the laser beams would have to be bent within a multi-duct cell to cover about 180 to 200 meters. This separator module would use overall laser light power of some 10 KW and could supply 3.5% enriched uranium in a single phase from natural uranium by rejecting 0.20% impoverished U. 27 refs [fr

  4. Over all separation factors for stable isotopes by gas centrifuge

    International Nuclear Information System (INIS)

    Chuntong Ying; Nie Yuguang; Zeng Shi; Shang Xiuyong; Wood, Houston G.

    1999-01-01

    The separation factor for the elements with molar wight differences, γ 0 , is an important characteristic parameter for separation of varied isotopes. Besides the dependence on construction parameters of the gas centrifuge it depends on many variables. Some of them are operation conditions, such as feeding flow rate F, pressure at wall p w , temperature T 0 and distribution temperature on the wall and others. Separation factor γ 0 depends on physical properties, such as molar weight M, viscosity μ, product of ρD, where ρ is density of working media and D is its diffusion coefficient. It was taken four examples: UF 6 , WF 6 , OsO 4 and Xe [ru

  5. Atomic collisions related to atomic laser isotope separation

    International Nuclear Information System (INIS)

    Shibata, Takemasa

    1995-01-01

    Atomic collisions are important in various places in atomic vapor laser isotope separation (AVLIS). At a vaporization zone, many atomic collisions due to high density have influence on the atomic beam characteristics such as velocity distribution and metastable states' populations at a separation zone. In the separation zone, a symmetric charge transfer between the produced ions and the neutral atoms may degrade selectivity. We have measured atomic excitation temperatures of atomic beams and symmetric charge transfer cross sections for gadolinium and neodymium. Gadolinium and neodymium are both lanthanides. Nevertheless, results for gadolinium and neodymium are very different. The gadolinium atom has one 5d electron and neodymium atom has no 5d electron. It is considered that the differences are due to existence of 5d electron. (author)

  6. Large scale gas chromatographic demonstration system for hydrogen isotope separation

    International Nuclear Information System (INIS)

    Cheh, C.H.

    1988-01-01

    A large scale demonstration system was designed for a throughput of 3 mol/day equimolar mixture of H,D, and T. The demonstration system was assembled and an experimental program carried out. This project was funded by Kernforschungszentrum Karlsruhe, Canadian Fusion Fuel Technology Projects and Ontario Hydro Research Division. Several major design innovations were successfully implemented in the demonstration system and are discussed in detail. Many experiments were carried out in the demonstration system to study the performance of the system to separate hydrogen isotopes at high throughput. Various temperature programming schemes were tested, heart-cutting operation was evaluated, and very large (up to 138 NL/injection) samples were separated in the system. The results of the experiments showed that the specially designed column performed well as a chromatographic column and good separation could be achieved even when a 138 NL sample was injected

  7. Controlled power supply for isotopes separator; Alimentations regulees pour separateur d'isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Lavaitte, A; Pottier, J [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1953-07-01

    This equipment is destined to equip the separator of isotopes who is the subject of the CEA report n 138. It includes: - a controlled power supply in voltage. - a controlled power supply in current. The spectra of fluctuations of these assembly is different in the two cases. (authors) [French] Cet equipement est destine a equiper le separateur d'isotopes qui fait l'objet du rapport C.E.A. n 138. Il comprend: - une alimentation regulee en tension. - une alimentation regulee en courant. Le spectre de fluctuations de ces ensembles est different dans les deux cas. (auteurs)

  8. The Laboratory for Laser Energetics’ Hydrogen Isotope Separation System

    Energy Technology Data Exchange (ETDEWEB)

    Shmayda, W.T., E-mail: wshm@lle.rochester.edu; Wittman, M.D.; Earley, R.F.; Reid, J.L.; Redden, N.P.

    2016-11-01

    The University of Rochester’s Laboratory for Laser Energetics has commissioned a hydrogen Isotope Separation System (ISS). The ISS uses two columns—palladium on kieselguhr and molecular sieve—that act in a complementary manner to separate the hydrogen species by mass. The 4-sL per day throughput system is compact and has no moving parts. The columns and the attendant gas storage and handling subsystems are housed in a 0.8 -m{sup 3} glovebox. The glovebox uses a helium cover gas that is continuously processed to extract oxygen and water vapor that permeates through the glovebox gloves and any tritium that is released while attaching or detaching vessels to add feedstock to or drawing product from the system. The isotopic separation process is automated and does not require manual intervention. A total of 315 TBq of tritium was extracted from 23.6 sL of hydrogen with tritium purities reaching 99.5%. Deuterium was the sole residual component in the processed gas. Raffinate contained 0.2 TBq of activity was captured for reprocessing. The total emission from the system to the environment was 0.4 GBq over three weeks.

  9. Influence of throttling of the heavy fraction on the uranium isotope separation in the separation nozzle

    International Nuclear Information System (INIS)

    Bley, P.; Ehrfeld, W.; Heiden, U.

    1978-04-01

    In a separation nozzle cascade for enrichment of U-235 the cut of the separation elements is adjusted by throttling the heavy fraction. This control process influences directly the flow properties in the nozzle and may noticeably change its separation characteristics. This paper deals with an experimental investigation of the throttling effect on the separation and control characteristics of the separation nozzle operated with a H 2 /UF 6 mixture. In consideration of the extremely small characteristic dimensions of commercial separation nozzle elements the influence of manufacturing tolerances on the characteristics of the throttled nozzle was analysed in detail. It appears, that the elementary effect of isotope separation increases by throttling of the heavy fraction up to 5% without changing the optimum operating conditions. This increase of the elementary effect is not only obtained for separation nozzles with zero tolerances but also for separation nozzles having finite tolerances of the skimmer position. Tolerances of the nozzle width, however, become increasingly detrimental, when the heavy fraction is throttled. Regarding the control characteristics of the separation nozzle it was found out, that the UF 6 -cut of the throttled nozzle reacts more sensitively to alterations of the operating pressures and less sensitively to alterations of the UF 6 -concentration of the process gas mixture. (orig.) [de

  10. High-Voltage Power Supply System for Laser Isotope Separation

    Energy Technology Data Exchange (ETDEWEB)

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

    1979-06-26

    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.

  11. High-Voltage Power Supply System for Laser Isotope Separation

    International Nuclear Information System (INIS)

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

    1979-01-01

    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

  12. Method for enriching and separating heavy hydrogen isotopes from substance streams containing such isotopes by means of isotope exchange

    International Nuclear Information System (INIS)

    Knochel, A.; Eggers, I.; Klatte, B.; Wilken, R. D.

    1985-01-01

    A process for enriching and separating heavy hydrogen isotopes having a heavy hydrogen cation (deuterium and/or tritium) from substance streams containing them, wherein the respectively present hydrogen isotopes are exchanged in chemical equilibria. A protic, acid solution containing deuterium and/or tritium is brought into contact with a value material from the group of open-chained polyethers or aminopolyethers, macro-monocyclic or macro-polycyclic polyethers, macro-monocyclic or macro-polycyclic amino polyethers, and mixtures of these values, in their free or proton salt form to form a reaction product of the heavy hydrogen cation with the value or value salt and bring about enrichment of deuterium and/or tritium in the reaction product. The reaction product containing the value or value salt is separated from the solution. The separated reaction product is treated to release the hydrogen isotope(s) to be enriched in the form of deuterium oxide (HDO) and/or tritium oxide (HTO) by regenerating the value or its salt, respectively. The regenerated value is returned for reuse

  13. Biomedical research applications of electromagnetically separated enriched stable isotopes

    International Nuclear Information System (INIS)

    Lambrecht, R.M.

    1982-01-01

    The current and projected annual requirements through 1985 for stable isotopes enriched by electromagnetic separation methods were reviewed for applications in various types of biomedical research: (1) medical radiosotope production, labeled compounds, and potential radiopharmaceuticals; (2) nutrition, food science, and pharmacology; (3) metallobiochemistry and environmental toxicology; (4) nuclear magnetic resonance, electron paramagnetic resonance, and Moessbauer spectroscopy in biochemical, biophysical, and biomedical research; and (5) miscellaneous advances in radioactive and non-radioactive tracer technology. Radioisotopes available from commercial sources or routinely used in clinical nuclear medicine were excluded. Priorities and summaries are based on statements in the references and from answers to a survey conducted in the fall of 1981. Current requirements for enriched stable isotopes in biomedical research are not being satisfied. Severe shortages exist for 26 Mg, 43 Ca, 70 Zn, 76 Se, 78 Se, 102 Pd, 111 Cd, 113 Cd, and 190 Os. Many interesting and potentially important investigations in biomedical research require small quantities of specific elements at high isotopic enrichments

  14. Separation of argon isotopes by porous membrane method, (2)

    International Nuclear Information System (INIS)

    Yoshida, Hiroshi; Fujine, Sachio; Saito, Keiichiro; Ouchi, Misao; Naruse, Yuji

    1979-08-01

    Separation characteristics of an engineering-scale cascade equipment, which is composed of five stages using Al 2 O 3 barriers, were examined under different operating conditions. This report describes the results of the separation experiment of argon isotopes by the square cascade operated under total reflux. The results are as follows: (1) Mean pore diameter and tortuosity of the barriers were estimated to be 400A and 13-15, respectively. (2) Flow mechanism through the barriers was proved to be ideal Knudsen flow by measurement of the permeability. (3) The cascade was equilibriated in 30-40 minutes, depending on stage gas inventory. (4) The effect of an operating pressure on the separation factor could be estimated by Knudsen's and Present-deBethune's theories. (5) The stage separation factor could be estimated by the conventional theoretical equations by introducing a correction factor as a function of Reynolds number of the permeating flow through the barriers. (6) An experimental equation to estimate the flow effect on the separation factor was obtained considering velocity and physical properties of the gas in the vicinity of the barrier surface. (author)

  15. On-line I{sup −}/Te{sup −} separation for the AMS analysis of {sup 125}I

    Energy Technology Data Exchange (ETDEWEB)

    Charles, C.R.J., E-mail: christopher.charles@uottawa.ca [Andre E. Lalonde Accelerator Mass Spectrometry Laboratory, Advanced Research Complex, University of Ottawa, 25 Templeton Street, Ottawa, ON K1N 6N5 (Canada); Cornett, R.J.; Zhao, X.-L. [Andre E. Lalonde Accelerator Mass Spectrometry Laboratory, Advanced Research Complex, University of Ottawa, 25 Templeton Street, Ottawa, ON K1N 6N5 (Canada); Litherland, A.E. [IsoTrace Laboratory, Department of Physics, University of Toronto, 60 St. George Street, Toronto, ON M5S 1A7 (Canada); Kieser, W.E. [Andre E. Lalonde Accelerator Mass Spectrometry Laboratory, Advanced Research Complex, University of Ottawa, 25 Templeton Street, Ottawa, ON K1N 6N5 (Canada)

    2015-10-15

    The isobar separator for anions (ISA) was used together with a 3 MV tandem accelerator mass spectrometer (AMS) to demonstrate the real time (on-line) separation of Te{sup −} from I{sup −}. Following the ion source mass spectrometry and major retardation to tens of eV, the ISA uses a radiofrequency quadrupole (RFQ) ion guide to confine and direct I{sup −} and associated Te{sup −} isobar anions through a gas-reaction cell, where chemical reactions occur at eV energies with the electronegative gas NO{sub 2}. Anions are subsequently reaccelerated out of the ISA to near original ion source extraction energies for AMS analysis. At 5 mTorr NO{sub 2} in the ISA gas-reaction cell, {sup 125}Te{sup −} was observed to be attenuated by a factor of ∼10{sup 7} as compared to {sup 127}I{sup −} that did not experience significant (<50%) losses. A comparative test using {sup 37}Cl{sup −} and {sup 32}S{sup −} (having similar chemical properties to iodine and tellurium) showed a {sup 32}S{sup −} attenuation of >10{sup 7} relative to {sup 37}Cl{sup −} under the same ISA–AMS conditions. The preferential destruction of Te{sup −} (and S{sup −}) at eV energies in the ISA is likely due to a larger favorable destruction cross-section with NO{sub 2}. This study is the first demonstration of I–Te anion separation for AMS, and makes possible the use of {sup 125}I, free of the contaminant {sup 125}Te isobar after suitable sample purification, for future {sup 129}I/{sup 125}I carrier-free analyses of natural samples at ultra-low trace levels.

  16. Next-generation TCAP hydrogen isotope separation process

    International Nuclear Information System (INIS)

    Heung, L. K.; Sessions, H. T.; Poore, A. S.; Jacobs, W. D.; Williams, C. S.

    2008-01-01

    A thermal cycling absorption process (TCAP) for hydrogen isotope separation has been in operation at Savannah River Site since 1994. The process uses a hot/cold nitrogen system to cycle the temperature of the separation column. The hot/cold nitrogen system requires the use of large compressors, heat exchanges, valves and piping that is bulky and maintenance intensive. A new compact thermal cycling (CTC) design has recently been developed. This new design uses liquid nitrogen tubes and electric heaters to heat and cool the column directly so that the bulky hot/cold nitrogen system can be eliminated. This CTC design is simple and is easy to implement, and will be the next generation TCAP system at SRS. A twelve-meter column has been fabricated and installed in the laboratory to demonstrate its performance. The design of the system and its test results to date is discussed. (authors)

  17. Separation and implantation of the rare isotope {sup 163}Ho

    Energy Technology Data Exchange (ETDEWEB)

    Kieck, Tom; Chrysalidis, Katerina; Dorrer, Holger; Kormannshaus, Stefan; Schmidt, Sebastian; Schneider, Fabian; Wendt, Klaus [JGU Mainz (Germany); Duellmann, Christoph [JGU Mainz (Germany); GSI Darmstadt (Germany); Gamer, Lisa; Gastaldo, Loredana [Universitaet Heidelberg (Germany); Collaboration: ECHo-Collaboration

    2016-07-01

    The ECHo collaboration aims at measuring the electron neutrino mass by recording the spectrum following electron capture of {sup 163}Ho. To reach a sub-eV sensitivity, a large number of individual microcalorimeters is needed, into which the isotope must be implanted in a well-controlled manner. The necessary amount of {sup 163}Ho is produced by neutron irradiation of enriched {sup 162}Er in the ILL high flux reactor. This introduces significant contaminations of other radioisotopes, which have to be quantitatively removed both, by chemical and mass spectrometric separation. The application of resonance ionization at the RISIKO mass separator guarantees the required isotope selectivity for purification and suitable energy for ion implantation. The efficiency and stability of the laser ion source was improved by Finite-Element Analysis of the thermal processes. For optimum implantation into the detector pixels (170 x 170 μm{sup 2}) with minimum losses a small ion beam spot at the implantation site is needed. For this purpose, post focusing ion optics were installed. Simulations were performed in order to optimize the homogeneous distribution of the implanted ions. The necessity to alternate implantation phases with deposition of a thin metallic layer for {sup 163}Ho activities larger than 10 Bq is being discussed.

  18. Charge exchange effect on laser isotope separation of atomic uranium

    International Nuclear Information System (INIS)

    Niki, Hideaki; Izawa, Yasukazu; Otani, Hiroyasu; Yamanaka, Chiyoe

    1982-01-01

    Uranium isotope separating experiment was performed using the two-step photoionization technique with dye laser and nitrogen laser by heating uranium metal with electron beam and producing atomic beam using generated vapour. The experimental results are described after explaining the two-step photoionization by laser, experimental apparatus, the selection of exciting wavelength and others. Enrichment factor depends largely on the spectrum purity of dye laser which is the exciting source. A large enrichment factor of 48.3 times was obtained for spectrum width 0.03A. To put the uranium isotope separation with laser into practice, the increase of uranium atomic density is considered to be necessary for improving the yield. Experimental investigation was first carried out on the charge exchange effect that seems most likely to affect the decrease of enrichment factor, and the charge exchange cross-section was determined. The charge exchange cross-section depends on the relative kinetic energy between ions and atoms. The experimental result showed that the cross-section was about 5 x 10 -13 cm 2 at 1 eV and 10 -13 cm 2 at 90 eV. These values are roughly ten times as great as those calculated in Lawrence Livermore Laboratory, and it is expected that they become the greatest factor for giving the upper limit of uranium atomic density in a process of practical application. (Wakatsuki, Y.)

  19. Isotopic separation of 13C by selective photodissociation of formaldehyde

    International Nuclear Information System (INIS)

    Mussillon, T.

    1998-01-01

    The aim of this work is to study the feasibility of the 13 C isotopic separation by UV laser spectroscopy. The spectra of H 2 12 CO and H 2 13 CO have been recorded by a Fourier transform spectrometer between 28000 and 34000 cm -1 . From these data has been carried out a systematic study of some lines by laser spectroscopy. The selectivity measurements have been compared with the obtained enrichment factors. Thus has been revealed in a quantitative way, the importance of the isotopic re-mixture phenomena and of the selectivity loss. The best enrichment factor has been measured at 29935,56 cm -1 (band: (2,14,1)). A final percentage of 42,1 % has been obtained in a reproducible way for 13 C. The evolution of the enrichment factor has been characterized for a pressure range between 4,4 and 43 mbar. Above the radical dissociation threshold, it has not be possible to show a positive effect of NO on the enrichment factor. This negative result has been explained by a detailed kinetic study of the radical reactions (available literature). This experimental study has been completed by a bibliographic synthesis for understanding the formaldehyde photochemistry. All the processes able to influence the performance of this isotopic separation process have been gathered in this work in an exhaustive way. The radical dissociation threshold of H 2 13 CO have been calculated from molecular constants of the literature and from known thermodynamic data for H 2 12 CO. (O.M.)

  20. First on-line mass measurements at SHIPTRAP and mass determinations of neutron-rich Fr and Ra isotopes at ISOLTRAP

    CERN Document Server

    Rahaman, Saidu

    SHIPTRAP is an ion trap facility behind the velocity filter SHIP at GSI/Darmstadt. Its aim are precision studies of transuranium nuclides produced in a fusion reaction and separated by SHIP. The current set-up for high-precision mass measurements consists of three main functional parts: (i) a gas cell for stopping the energetic ions from SHIP, (ii) radiofrequency quadrupole structures to cool and to bunch the ions extracted from the gas cell, and (iii) a superconducting magnet with two cylindrical Penning traps at a field strength of 7 T. In this work the Penning trap system has been installed and extensively characterized. The first on-line mass measurements of short-lived nuclides were carried out and the masses of $^{147}$Er and $^{148}$Er could be experimentally determined for the first time. Here a relative mass uncertainty of $\\delta$ m/m of about 1$\\times$ 10$^{-6}$ was achieved. Furthermore the masses of heavy neutron-rich $^{229-232}$Ra and $^{230}$Fr isotopes have been determined with a relative m...

  1. Isotopic separation by centrifugation. Rotating plasma; Separacion Isotopic por Centrifugacion Plasma Rotante

    Energy Technology Data Exchange (ETDEWEB)

    Perello, M; Vigon, M A

    1972-07-01

    The motion of a gas simultaneously submitted to an electric discharge and magnetic field has been studied in order to analyze the possibility of producing isotopes separation by rotation of a plasma. Some experimental results obtained under different discharge conditions are also given. Differences of pressure up to 15 mm oil between both electrodes has been attained. No definite conclusion on separation factors could be reached because of the low reproducibility of results, probably due to the short duration of the discharge with a new chamber designed to support stronger thermal shocks more reliable data can be expected. (Author) 16 refs.

  2. On-line coupling of sample preconcentration by LVSEP with gel electrophoretic separation on T-channel chips.

    Science.gov (United States)

    Kitagawa, Fumihiko; Kinami, Saeko; Takegawa, Yuuki; Nukatsuka, Isoshi; Sueyoshi, Kenji; Kawai, Takayuki; Otsuka, Koji

    2017-01-01

    To achieve an on-line coupling of the sample preconcentration by a large-volume sample stacking with an electroosmotic flow pump (LVSEP) with microchip gel electrophoresis (MCGE), a sample solution, a background solution for LVSEP and a sieving solution for MCGE were loaded in a T-form channel and three reservoirs on PDMS microchips. By utilizing the difference in the flow resistance of the two channels, a low-viscosity sample and a viscous polymer solution were easily introduced into the LVSEP and MCGE channels, respectively. Fluorescence imaging of the sequential LVSEP-MCGE processes clearly demonstrated that a faster stacking of anionic fluorescein and successive introduction into the MCGE channel can be carried out on the T-channel chip. To evaluate the preconcentration performance, a conventional MCZE analysis of fluorescein on the cross-channel chip was compared with LVSEP-MCGE on the short T-channel chip, and as a result that the value of sensitive enhancement factor (SEF) was estimated to be 370. The repeatability of the peak height was good with the RSD value of 3.2%, indicating the robustness of the enrichment performance. In the successive LVSEP-MCGE analysis of φX174/HaeIII digest, the DNA fragments were well enriched to a sharp peak in the LVSEP channel, and they were separated in the MCGE channel, whose electropherogram was well-resembled with that in the conventional MCGE. The values of SEF for the DNA fragments were calculated to be ranging from 74 to 108. Thus, the successive LVSEP-MCGE analysis was effective for both preconcentrating and separating DNA fragments. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  3. Nuclear proliferation using laser isotope separation - Verification options

    International Nuclear Information System (INIS)

    Erickson, Stanley A.

    2001-01-01

    Full text: This paper discusses the use of laser isotope separation techniques for the purpose of nuclear proliferation by a Non-Nuclear Weapons State (NNWS) that is a signatory of the Non- Proliferation Treaty (NPT) and is subject to inspections by the IAEA. It includes an analysis of the feasibility of the technique by a NNWS, what conditions are necessary for success, what would be required for either the use of the technique as a covert enrichment method or its use as a non-declared adjunct to a declared enrichment facility, and what signs might be available for the detection of such activity. The Atomic Vapor Laser Isotope Separation (AVLIS) technology, developed by LLNL from 1973 through 1999, is used as a concrete example to allow more determination of the questions of feasibility, requirements, and signatures, as this technology has been further developed than others, and has been documented extensively. The question of feasibility of the technique for the enrichment of significant quantities of uranium or plutonium to produce weapons-grade materials is investigated by decomposing the development necessary for the technique into steps that can be analyzed for requirements, both in expertise, equipment, and scientific knowledge. The paper concludes that the technique is usable for proliferation, although with difficulty, by some nations during the next two decades. The technique may be developed in a completely covert method, with no declarations and no public indication that it is under research and development, or alternatively, some admissions may be made to allow or promote exchange of information. The technique can be disclosed as a research and development technology for the separation of non-radioactive isotopes, for the separation of radioactive isotopes including those in commercial use for medical or industrial purposes, or as part of a nuclear fuel cycle. The ability to translate development work from the first two of these to a system usable for

  4. Modeling of hydrogen isotopes separation in a metal hydride bed

    International Nuclear Information System (INIS)

    Charton, S.; Corriou, J.P.; Schweich, D.

    1999-01-01

    A predictive model for hydrogen isotopes separation in a non-isothermal bed of unsupported palladium hydride particles is derived. It accounts for the non-linear adsorption-dissociation equilibrium, hydrodynamic dispersion, pressure drop, mass transfer kinetics, heat of sorption and heat losses at the bed wall. Using parameters from the literature or estimated with classical correlations, the model gives simulated curves in agreement with previously published experiments without any parameter fit. The non-isothermal behavior is shown to be responsible for drastic changes of the mass transfer rate which is controlled by diffusion in the solid-phase lattice. For a feed at 300 K and atmospheric pressure, the endothermic hydride-to-deuteride exchange is kinetically controlled, whereas the reverse exothermic exchange is nearly at equilibrium. Finally, a simple and efficient thermodynamic model for the dissociative equilibrium between a metal and a diatomic gas is proposed. (Copyright (c) 1999 Elsevier Science B.V., Amsterdam. All rights reserved.)

  5. Efficiencies of laser dyes for atomic vapor laser isotope separation

    International Nuclear Information System (INIS)

    Maeda, Mitsuo; Oki, Yuji; Uchiumi, Michihiro; Takao, Takayuki; Igarashi, Kaoru; Shimamoto, Kojiro.

    1995-01-01

    Efficiencies of 30 laser dyes for the atomic vapor laser isotope separation (AVLIS) are experimentally evaluated with a dye laser pumped by a frequency-doubled Nd:YAG laser. On the other hand, a simulation code is developed to describe the laser action of Rhodamine 6G, and the dependence of the laser efficiency on the pump wavelength is calculated. Following conclusions are obtained by these considerations:space: 1) Pyrromethene 567 showed 16% higher laser efficiency than Rhodamine 6G by 532 nm pumping, and Pyrromethene 556 has an ability to provide better efficiency by green light pumping with a Cu vapor laser; 2) Kiton red 620 and Rhodamine 640, whose efficiencies were almost the same as Rhodamine 6G by 532 nm pumping, will show better efficiencies by two-wavelength pumping with a Cu vapor laser. (author)

  6. Separated isotopes: vital tools for science and medicine

    International Nuclear Information System (INIS)

    1982-01-01

    Deliberations and conclusions of a Workshop on Stable Isotopes and Derived Radioisotopes organized by the Subcommittee on Nuclear and Radiochemistry of the National Research Council's Committee on Chemical Sciences at the request of the Department of Energy (DOE) are summarized. The workshop was jointly supported by the National Institutes of Health and DOE's Office of Basic Energy Sciences. An overview with three recommendations resulting from the Workshop is followed by reports of the four Workshop panels. Background papers were prepared by individuals on the Steering Committee and made available to all participants prior to the Workshop. They are reproduced as Appendixes 3 to 8. Short reports on alternate separation techniques were presented at the Workshop and are reproduced in Appendixes 9 to 11

  7. Managing a major R et D program: isotope separation

    International Nuclear Information System (INIS)

    Ferrari, A.

    1988-01-01

    After the choice (in 1969) of the pressurized water type reactors which use enriched uranium, it became imperative for France to have facilities to enrich the uranium. The choice of the industrial process, the correlative decisions related to research and development and the search for alliances with partners abroad in a disturbed and changing energy context are retraced in this article. The choice of the Eurodif plant was the gaseous diffusion process. It still remains necessary to maintain research efforts concerning competitive technologies, i.e. ultracentrifuging and chemical process. The oil crisis augured well for massive recourse to nuclear energy. Then there was a cut-back in nuclear programs and enrichment capacities became lastingly higher than needs. So it became necessary to optimally pilot a selection of research paths, with long term orientation. The techniques, based on the use of the laser, provide an advance glimpse of major, even spectacular prospects of lowering the costs of isotope separation [fr

  8. Tritium Isotope Separation Using Adsorption-Distillation Column

    International Nuclear Information System (INIS)

    Fukada, Satoshi

    2005-01-01

    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, α H-T equi . The adsorption action improved not only HETP but also α H-T 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

  9. Separated isotopes: vital tools for science and medicine

    Energy Technology Data Exchange (ETDEWEB)

    1982-01-01

    Deliberations and conclusions of a Workshop on Stable Isotopes and Derived Radioisotopes organized by the Subcommittee on Nuclear and Radiochemistry of the National Research Council's Committee on Chemical Sciences at the request of the Department of Energy (DOE) are summarized. The workshop was jointly supported by the National Institutes of Health and DOE's Office of Basic Energy Sciences. An overview with three recommendations resulting from the Workshop is followed by reports of the four Workshop panels. Background papers were prepared by individuals on the Steering Committee and made available to all participants prior to the Workshop. They are reproduced as Appendixes 3 to 8. Short reports on alternate separation techniques were presented at the Workshop and are reproduced in Appendixes 9 to 11.

  10. Uranium isotope separation by gaseous diffusion and plant safety

    International Nuclear Information System (INIS)

    Simeon, Claude; Dumas, Maurice.

    1980-07-01

    This report constitutes a safety guide for operators of uranium isotope separation plants, and includes both aspects of safety and protection. Taking into account the complexity of safety problems raised at design and during operation of plants which require specialized guides, this report mainly considers both the protection of man, the environment and goods, and the principles of occupational safety. It does not claim to be comprehensive, but intends to state the general principles, the particular points related to the characteristics of the basic materials and processes, and to set forth a number of typical solutions suitable for various human and technical environments. It is based on the French experience gained during the last fifteen years [fr

  11. Laser separating system for production of zinc isotopes

    International Nuclear Information System (INIS)

    Bokhan, P.A.; Zakrevskij, D.Eh.; Stepanov, A.Yu.; Fateev, N.V.

    2000-01-01

    The separating system, which provides using the photochemical reaction of Zn at the long-lived Zn(4p 3 P j ) state with the CO 2 molecule was constructed. The reaction constant is equal to k = 2.5 · 10 -10 cm 3 c -1 . For production of selectively excited atoms the excitation of Zn at the Zn(6s 3 S 1 ) state by two counter UV photons followed by its decomposition at the Zn(4p 3 P j ) state was used. The feature of the used scheme of the Zn excitation provides the appearance of super-radiation on the cascades of transitions from the 6s 3 S 1 at 6p 3 P 1 0 state. The high selectivity of the consumption, the productivity of the system by the 66 Zn isotope exceeds over 0.5 g/h [ru

  12. Design study of fuel circulating system using Pd-alloy membrane isotope separation method

    International Nuclear Information System (INIS)

    Naito, T.; Yamada, T.; Yamanaka, T.; Aizawa, T.; Kasahara, T.; Nishikawa, M.; Asami, N.

    1980-01-01

    Design study on the fuel circulating system (FCS) for a tokamak experimental fusion reactor (JXFR) has been carried out to establish the system concept, to plan the development program, and to evaluate the feasibility of diffusion system. The FCS consists of main vacuum system, fuel gas refiners, isotope separators, fuel feeders, and auxiliary systems. In the system design, Pd-alloy membrane permeation method is adopted for fuel refining and isotope separating. All impurities are effectively removed and hydrogen isotopes are sufficiently separated by Pd-alloy membrane. The isotope separation system consists of 1st (47 separators) and 2nd (46 separators) cascades for removing protium and separating deuterium, respectively. In the FCS, while cryogenic distillation method appears to be practicable, Pd-alloy membrane diffusion method is attractive for isotope separation and refining of fuel gas. The choice will have to be based on reliability, economic, and safety analyses

  13. Innovative lasers for uranium isotope separation. [Progress report

    Energy Technology Data Exchange (ETDEWEB)

    Brake, M.L.; Gilgenbach, R.M.

    1991-06-01

    Copper vapor lasers have important applications to uranium atomic vapor laser isotope separation (AVLIS). The authors have spent the first two years of their project investigating two innovative methods of exciting/pumping copper vapor lasers which have the potential to improve the efficiency and scaling of large laser systems used in uranium isotope separation. Experimental research has focused on the laser discharge kinetics of (1) microwave, and (2) electron beam excitation/pumping of large-volume copper vapor lasers. During the first year, the experiments have been designed and constructed and initial data has been taken. During the second year these experiments have been diagnosed. Highlights of some of the second year results as well as plans for the future include the following: Microwave resonant cavity produced copper vapor plasmas at 2.45 GHz, have been investigated. A CW (0--500 W) signal heats and vaporizes the copper chloride to provide the atomic copper vapor. A pulsed (5 kW, 0.5--5kHz) signal is added to the incoming CW signal via a hybrid mixer to excite the copper states to the laser levels. An enhancement of the visible radiation has been observed during the pulsed pardon of the signal. Electrical probe measurements have been implemented on the system to verify the results of the electromagnetic model formulated last year. Laser gain measurements have been initiated with the use of a commercial copper vapor laser. Measurements of the spatial profile of the emission are also currently being made. The authors plan to increase the amount of pulsed microwave power to the system by implementing a high power magnetron. A laser cavity will be designed and added to this system.

  14. Flow dynamics in distillation columns packed with Dixon rings as used in isotope separation

    International Nuclear Information System (INIS)

    Gilath, C.; Cohen, H.; Wolf, D.

    1977-01-01

    Packed distillation columns are common in isotope separation. The pressure drop serves as an indication for the hydrodynamic state of the column. Models were formulated for flow and pressure drop dynamics in packed distillation columns. These models were confirmed on columns packed with Dixon rings and operated with water for separation of oxygen isotopes. Liquid holdup displacement is very important in isotope separation practice. Experiments proved that distillation columns packed with Dixon rings exhibit a behaviour close to plug flow. (author)

  15. Characteristics of isotope-selective chemical reactor with gas-separating device

    International Nuclear Information System (INIS)

    Gorshunov, N.M.; Kalitin, S.A.; Laguntsov, N.I.; Neshchimenko, Yu.P.; Sulaberidze, G.A.

    1988-01-01

    A study was made on characteristics of separating stage, composed of isotope-selective chemical (or photochemical) reactor and membrane separating cascade (MSC), designated for separation of isotope-enriched products from lean reagents. MSC represents the counterflow cascade for separation of two-component mixtures. Calculations show that for the process of carton isotope separation the electric power expences for MSC operation are equal to 20 kWxh/g of CO 2 final product at 13 C isotope content in it equal to 75%. Application of the membrane gas-separating cascade at rather small electric power expenses enables to perform cascading of isotope separation in the course of nonequilibrium chemical reactions

  16. ITER hydrogen isotope separation system conceptual design description

    International Nuclear Information System (INIS)

    Busigin, A.; Sood, S.K.; Kveton, O.K.; Dinner, P.J.; Murdoch, D.K.; Leger, D.

    1990-01-01

    This paper presents integrated hydrogen Isotope Separation System (ISS) designs for ITER based on requirements for plasma exhaust processing, neutral beam injection deuterium cleanup, pellet injector propellant detritiation, waste water detritiation, and breeding blanket detritiation. Specific ISS designs are developed for a machine with an aqueous lithium salt blanket (ALSB) and a machine with a solid ceramic breeding blanket (SBB). The differences in the ISS designs arising from the different blanket concepts are highlighted. It is found that the ISS designs for the two blanket concepts considered are very similar with the only major difference being the requirement for an additional large water distillation column for ALSB water detritiation. The extraction of tritium from the ALSB is based on flash evaporation to separate the blanket water from the dissolved Li salt, with the tritiated water then being fed to the ISS for detritiation. This technology is considered to be relatively well understood in comparison to front-end processes for SBB detritiation. In the design of the cryogenic distillation portion of the ISS, it was found that the tritium inventory could be very large (> 600 g) unless specific design measures were taken to reduce it. In the designs which are presented, the tritium inventory has been reduced to about 180 g, which is less than the ITER single-failure release limit of 200 g. Further design optimization and isolation of components is expected to reduce the inventory further. (orig.)

  17. Uranium isotope separation in the solid state. Final report for period ending September 30, 1978

    International Nuclear Information System (INIS)

    Bernstein, E.R.

    1978-09-01

    The final results of an investigation on the isotope separation of uranium in the solid state are presented in this report. The feasibility of separating uranium isotopes using the proposed system based on uranium borohydride (borodeuteride) in a low temperature mixed crystal has been determined. The first section of the report summarizes the background material relating to this work which includes: a calculation of isotope shifts (borodeuteride), details on the two-step, two-photon spectroscopic isotope separation technique, and a brief overview of the method and equipment used for separating uranium isotopes in the solid state. The second section concerns the experimental details of the present work performed in the laboratory. Representative spectroscopic data obtained in this investigation are presented and discussed in the third section. Finally, the report is concluded with recommendations for further investigations on the uranium borohydride (borodeuteride) system for isotope separation

  18. On-line gas chromatography combustion/pyrolysis isotope ratio mass spectrometry (HRGC-C/P-IRMS) of pineapple (Ananas comosus L. Merr.) volatiles.

    Science.gov (United States)

    Preston, Christina; Richling, Elke; Elss, Sandra; Appel, Markus; Heckel, Frank; Hartlieb, Ariane; Schreier, Peter

    2003-12-31

    By use of extracts prepared by liquid-liquid separation of the volatiles from self-prepared juices of pineapple fruits (Ananas comosus) (n = 14) as well as commercial pineapple recovery aromas/water phases (n = 3), on-line capillary gas chromatography-isotope ratio mass spectrometry was employed in the combustion (C) and the pyrolysis (P) modes (HRGC-C/P-IRMS) to determine the delta(13)C(VPDB) and delta(2)H(VSMOW) values of selected pineapple flavor constituents. In addition to methyl 2-methylbutanoate 1, ethyl 2-methylbutanoate 2, methyl hexanoate 3, ethyl hexanoate 4, and 2,5-dimethyl-4-methoxy-3[2H]-furanone 5, each originating from the fruit, the delta(13)C(VPDB) and delta(2)H(VSMOW) data of commercial synthetic 1-5 and "natural" (biotechnologically derived) 1-4 were determined. With delta(13)C(VPDB) data of pineapple volatiles 1-4 varying from -12.8 to -24.4 per thousand, the range expected for CAM metabolism was observed. Compound 5 showed higher depletion from -20.9 to -28.6 per thousand. A similar situation was given for the delta(2)H(VSMOW) values of 3-5 from pineapple ranging from -118 to -191 per thousand, whereas 1 and 2 showed higher depleted values from -184 to -263 per thousand. In nearly all cases, analytical differentiation of 1-5 from pineapple and natural as well as synthetic origin was possible. In general, natural and synthetic 1-5 exhibited delta(13)C(VPDB) data ranging from -11.8 to -32.2 per thousand and -22.7 to -35.9 per thousand, respectively. Their delta(2)H(VSMOW) data were in the range from -242 to -323 per thousand and -49 to -163 per thousand, respectively.

  19. Effects of GC temperature and carrier gas flow rate on on-line oxygen isotope measurement as studied by on-column CO injection.

    Science.gov (United States)

    Chen, Zhi-Gang; Yin, Xi-Jie; Zhou, Youping

    2015-08-01

    Although deemed important to δ 18 O measurement by on-line high-temperature conversion techniques, how the GC conditions affect δ 18 O measurement is rarely examined adequately. We therefore directly injected different volumes of CO or CO-N 2 mix onto the GC column by a six-port valve and examined the CO yield, CO peak shape, CO-N 2 separation, and δ 18 O value under different GC temperatures and carrier gas flow rates. The results show the CO peak area decreases when the carrier gas flow rate increases. The GC temperature has no effect on peak area. The peak width increases with the increase of CO injection volume but decreases with the increase of GC temperature and carrier gas flow rate. The peak intensity increases with the increase of GC temperature and CO injection volume but decreases with the increase of carrier gas flow rate. The peak separation time between N 2 and CO decreases with an increase of GC temperature and carrier gas flow rate. δ 18 O value decreases with the increase of CO injection volume (when half m/z 28 intensity is rate. On average, the δ 18 O value of the injected CO is about 1‰ higher than that of identical reference CO. The δ 18 O distribution pattern of the injected CO is probably a combined result of ion source nonlinearity and preferential loss of C 16 O or oxygen isotopic exchange between zeolite and CO. For practical application, a lower carrier gas flow rate is therefore recommended as it has the combined advantages of higher CO yield, better N 2 -CO separation, lower He consumption, and insignificant effect on δ 18 O value, while a higher-than-60 °C GC temperature and a larger-than-100 µl CO volume is also recommended. When no N 2 peak is expected, a higher GC temperature is recommended, and vice versa. Copyright © 2015 John Wiley & Sons, Ltd. Copyright © 2015 John Wiley & Sons, Ltd.

  20. Radioactive isotope and isomer separation with using light induced drift effect

    International Nuclear Information System (INIS)

    Hradecny, C.; Slovak, J.; Tethal, T.; Ermolaev, I.M.; Shalagin, A.M.

    1991-01-01

    The isotope separation with using light induced drift (LID) is discussed. The basic theoretical characteristics of the method are deduced: separation simultaneously with an arbitrary high enrichment and without significant losses; separation productivity up to 100 μg/h. These characteristics are sufficient and very convenient for separation of expensive radioactive isotopes and isomers which are applied in medicine and science. The first experimental separation of the radioactive isotopes ( 22,24 Na) by using the LID effect is reported. 13 refs.; 5 figs

  1. First on-line applications of a multi-reflection time-of-flight mass separator at ISOLTRAP and the mass measurement of 82Zn

    International Nuclear Information System (INIS)

    Wolf, Robert

    2013-01-01

    This thesis describes the implementation and first on-line application of a multi-reflection time-of-flight (MR-ToF) mass analyzer for high-resolution mass separation at the ISOLTRAP mass spectrometer at ISOLDE/CERN. On the one hand, the major objective was to improve ISOLTRAPs mass-measurement capabilities with respect to the ratio of delivered contaminating ions to ions of interest. On the other hand, the time necessary to purify wanted from unwanted species should be reduced as much as possible to enable access to even more exotic nuclei. The device has been set up, optimized and tested at the University of Greifswald before its move to ISOLTRAP. The achieved performance comprises mass resolving powers of up to 2 x 10 5 reached at observation times of 30 ms and a contamination suppression of about four orders of magnitude by use of a Bradbury-Nielsen gate. With the characteristics, it outperforms clearly the so far state-of-the-art purification method of a gas-filled Penning trap. To improve the utilization of the MR-ToF mass analyzer, the in-trap lift method has been developed. It simplifies the application and optimization of the device, which is a crucial time factor in an on-line experiment. The device was the first of its kind successfully applied to radioactive ion beams for a mass analysis, for a mass separation (in combination with the Bradbury-Nielsen gate) as a preparatory step for a subsequent Penning-trap mass measurement and as a high-precision mass spectrometer of its own. The later was recently used for the first mass measurement of the neutron-rich calcium isotopes 53 Ca and 54 Ca. The so-far achieved mass-resolving power of 2 x 10 5 belongs to the highest reported for time-of-flight mass analyzers at all. The first successful application of the MR-ToF system as the only mass separator at ISOLTRAP resulted in the mass measurement of 82 Zn. The new mass value has been compared to mass extrapolations of the most recent Hartree-Fock-Bogolyubov (HFB

  2. LACAN Code for global simulation of SILVA laser isotope separation process

    International Nuclear Information System (INIS)

    Quaegebeur, J.P.; Goldstein, S.

    1991-01-01

    Functions used for the definition of a SILVA separator require quite a lot of dimensional and operating parameters. Sizing a laser isotope separation plant needs the determination of these parameters for optimization. In the LACAN simulation code, each elementary physical process is described by simplified models. An example is given for a uranium isotope separation plant whose separation power is optimized with 6 parameters [fr

  3. Study on atmospheric hydrogen enrichment by cryopump method and isotope separation by gas chromatography

    International Nuclear Information System (INIS)

    Taniyama, Yuki; Momoshima, Noriyuki

    2001-01-01

    To obtain the information of source of atmospheric hydrogen tritium an analysis of tritium isotopes is thought to be effective. So an atmospheric hydrogen enrichment apparatus and a cryogenic gas chromatographic column were made. Experiments were carried out to study the performance of cryopump to enrich atmospheric hydrogen and the column to separate hydrogen isotopes that obtained by cryopump method. The cryopump was able to process about 1000 1 atmosphere and the column was able to separate hydrogen isotopes with good resolution. (author)

  4. Separated isotopes: vital tools for science and medicine

    International Nuclear Information System (INIS)

    1982-01-01

    This report summarizes the deliberations and conclusions of a Workshop on Stable Isotopes and Derived Radioisotopes organized by the Subcommittee on Nuclear and Radiochemistry of the National Research Council's Committee on Chemical Sciences at the request of the Department of Energy (DOE). The workshop was jointly supported by the National Institutes of Health and DOE's Office of Basic Energy Sciences. An Overview with three recommendations resulting from the Workshop, prepared by the Steering Committee, is followed by Chapters 1 to 4, reports of the following four Workshop panels: (1) panel on research applications in physics, chemistry and geoscience; (2) panel on commercial applications; (3) panel on biomedical research applications; (4) panel on clinical applications. Background papers were prepared by individuals on the Steering Committee and made available to all participants prior to the Workshop. They proved of great value and are reproduced as Appendixes 3 to 8. Short reports on alternate separation techniques were presented at the Workshop and are reproduced in Appendixes 9 to 11. Selected papers have been abstracted and indexed

  5. Development of an on-line mixed-mode gel liquid chromatography×reversed phase liquid chromatography method for separation of water extract from Flos Carthami.

    Science.gov (United States)

    Wang, Yu-Qing; Tang, Xu; Li, Jia-Fu; Wu, Yun-Long; Sun, Yu-Ying; Fang, Mei-Juan; Wu, Zhen; Wang, Xiu-Min; Qiu, Ying-Kun

    2017-10-13

    A novel on-line comprehensive two-dimensional liquid chromatography (2D-LC) method by coupling mixed-mode gel liquid chromatography (MMG-LC) with reversed phase liquid chromatography (RPLC) was developed. A mixture of 17 reference compounds was used to study the separation mechanism. A crude water extract of Flos Carthami was applied to evaluate the performance of the novel 2D-LC system. In the first dimension, the extract was eluted with a gradient of water/methanol over a cross-linked dextran gel Sephadex LH-20 column. Meanwhile, the advantages of size exclusion, reversed phase partition and adsorption separation mechanism were exploited before further on-line reversed phase purification on the second dimension. This novel on-line mixed-mode Sephadex LH-20×RPLC method provided higher peak resolution, sample processing ability (2.5mg) and better orthogonality (72.9%) versus RPLC×RPLC and hydrophilic interaction liquid chromatography (HILIC)×RPLC. To the best of our knowledge, this is the first report of a mixed-mode Sephadex LH-20×RPLC separation method with successful applications in on-line mode, which might be beneficial for harvesting targets from complicated medicinal plants. Copyright © 2017 Elsevier B.V. All rights reserved.

  6. Cascade theory in isotopic separation processes; Theorie des cascades en separation isotopique

    Energy Technology Data Exchange (ETDEWEB)

    Agostini, J P

    1994-06-01

    Three main areas are developed within the scope of this work: - the first one is devoted to fundamentals: separative power, value function, ideal cascade and square cascade. Applications to two main cases are carried out, namely: Study of binary isotopic mix, Study of processes with a small enrichment coefficient. - The second one is devoted to cascade coupling -high-flux coupling (more widely used and better known) as well as low-flux coupling are presented and compared to one another. - The third one is an outlook on problems linked to cascade transients. Those problem are somewhat intricate and their interest lies mainly into two areas: economics where the start-up time may have a large influence on the interests paid during the construction and start-up period, military productions where the start-up time has a direct bearing on the production schedule. (author). 50 figs. 3 annexes. 12 refs. 6 tabs.

  7. Sulfur isotope separation by anion exchange chromatography: 34 S isotope enrichment

    International Nuclear Information System (INIS)

    Bendassolli, Jose Albertino; Trivelin, Paulo Cesar O.; Carneiro Junior, Francisco

    1995-01-01

    The 34 S isotope separation was carried out by isotopic exchange reactions between sulphurous acid in solution and bisulphite anions adsorbed on an ammonium quaternary (Dowex 1 x 8 and Dowex 2 x 8, 100-200 mesh) anion exchange resin packed in columns. Each resin column had 130 cm length and 2.2 cm diameter. The columns were connected in series during displacement of bisulphite bands. For the experiments, a band of bisulphite was fixed to the anion resin, initially in the hydroxyl ion form, and subsequently eluted with 0.2 0.3, 0.4 and 0.6 mol L -1 HCL solution. The hydrochloric acid solution was kept under a nitrogen atmosphere at 245 KPa of pressure, in order to prevent the evolution of gases and also the oxidation of the bisulphite. The experiments showed that the best results were obtained with the elution of bisulphite with 0.2 mol.L -1 HCL, with the Dowex 1 x 8 resin. Enrichments in 34 S of 17.33 atoms% were obtained using Dowex 1 x 8 resin, 0.2 mol.L -1 HCL solution and band displacement of 50 m. Replacing the depleted portion of the band with natural bisulphite, for each 10 m of band displacement, produced 6.79 mmol of sulphurous acid enriched with approximately 17% of 34 S, after 14 m of band dislocation. (author). 7 refs., 1 fig., 2 tabs

  8. The future of producing separated stable isotopes at Oak Ridge National Laboratory for accelerator applications

    International Nuclear Information System (INIS)

    Collins, E.D.

    1994-01-01

    Separated stable isotopes, produced in the calutrons at Oak Ridge National Laboratory, are essential target materials for production of numerous radioisotopes in accelerators and reactors. Recently, separated stable isotope production has been curtailed because government appropriations were discontinued and salts revenues decreased. The calutrons were placed in standby and the operating staff reduced to enable support by sales from existing inventories. Appeals were made to industry and government to preserve this national capability. Methods for providing volume-based price reductions were created to attract support from commercial isotope users. In 1994, the Department of Energy's Isotope Production and Distribution Program was restructured and a strategy produced to seek appropriated funding for the future production of rare, nonprofitable isotopes for research uses. This strategy, together with new demands for medical isotopes, will enable future operation of the calutrons. Moreover, production may be enhanced by complementing calutron capabilities with the Plasma Separation Process

  9. Laser separation of nitrogen isotopes by the IR+UV dissociation of ammonia molecules

    International Nuclear Information System (INIS)

    Apatin, V M; Klimin, S A; Laptev, V B; Lokhman, V N; Ogurok, D D; Pigul'skii, S V; Ryabov, E A

    2008-01-01

    The separation of nitrogen isotopes is studied upon successive single-photon IR excitation and UV dissociation of ammonia molecules. The excitation selectivity was provided by tuning a CO 2 laser to resonance with 14 NH 3 molecules [the 9R(30) laser line] or with 15 NH 3 molecules [the 9R(10) laser line]. Isotopic mixtures containing 4.8% and 0.37% (natural content) of the 15 NH isotope were investigated. The dependences of the selectivity and the dissociation yield for each isotopic component on the buffer gas pressure (N 2 , O 2 , Ar) and the ammonia pressure were obtained. In the limit of low NH 3 pressures (0.5-2 Torr), the dissociation selectivity α(15/14) for 15 N was 17. The selectivity mechanism of the IR+UV dissociation is discussed and the outlook is considered for the development of the nitrogen isotope separation process based on this approach. (laser isotope separation)

  10. Production of neutron deficient rare isotope beams at IGISOL; on-line and off-line studies

    NARCIS (Netherlands)

    Huikari, J; Dendooven, P; Jokinen, A; Nieminen, A; Penttila, H; Perajarvi, K; Popov, A; Rinta-Antila, S; Aysto, J

    This article reports on recent on-line yield measurements employing the light-ion and heavy-ion reaction-based ion guide systems and new results on a-recoil ion transport properties in ion guides with and without electric fields. In addition, the presently used ion guide designs for fusion

  11. Determination of the separation factor of uranium isotopes by gaseous diffusion; Determination des facteurs de separation des isotopes de l'uranium par diffusion gazeuse

    Energy Technology Data Exchange (ETDEWEB)

    Bilous, O; Counas, G [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1958-07-01

    A 12-stage pilot separation cascade with a low output has been constructed to measure the separation factor of uranium isotopes by gaseous diffusion. The report describes some of the separation results obtained, and also provides information on the time necessary for equilibrium to be established and on the influence of various perturbations on the pressure profile in the cascade. (author) [French] Une cascade pilote de 12 etages de separation a faible debit a ete construite pour mesurer le facteur de separation des isotopes de l'uranium par diffusion gazeuse. Le rapport decrit certains des resultats de separation obtenus et fournit egalement des donnees sur les temps de mise en equilibre et l'influence de diverses perturbations sur le profil des pressions dans la cascade. (auteur)

  12. On-line nuclear orientation

    International Nuclear Information System (INIS)

    Krane, K.S.

    1990-01-01

    This grant has as its overall goal the pursuit of on-line nuclear orientation experiments for the purpose of eliciting details of nuclear structure from the decays of neutron-deficient nuclei, such as those produced by the Holifield Heavy-Ion Research Facility at Oak Ridge and extracted by the UNISOR Isotope Separator. This paper discusses: refrigerator development; the decay of 184 Au; the decay of 191 Hg to 191 Au; the decay of 189 Pt to 189 Ir; the decays of 109,111 Pd; the decay of 172 Er; and solid angle corrections

  13. Mathematical model of nonstationary hydraulic processes in gas centrifuge cascade for separation of multicomponent isotope mixtures

    OpenAIRE

    Orlov, Aleksey Alekseevich; Ushakov, Anton; Sovach, Victor

    2017-01-01

    The article presents results of development of a mathematical model of nonstationary hydraulic processes in gas centrifuge cascade for separation of multicomponent isotope mixtures. This model was used for the calculation parameters of gas centrifuge cascade for separation of silicon isotopes. Comparison of obtained values with results of other authors revealed that developed mathematical model is adequate to describe nonstationary hydraulic processes in gas centrifuge cascades for separation...

  14. The outline of the processes for lithium isotope separation by ion exchange method

    International Nuclear Information System (INIS)

    Fujine, Sachio; Saito, Keiichiro; Naruse, Yuji; Shiba, Koreyuki; Kosuge, Masao; Itoi, Toshiaki; Kitsukawa, Tomohiko.

    1981-10-01

    A plant of lithium isotope separation by displacement chromatography is preliminary designed. The construction expenses of a 100 kg 7 Li/year plant and the unit cost of separation are estimated on the basis of the data taken from the literature, and the feasibility is studied. Experimental equipment of continuous displacement chromatography is set up and is tested with the stable automatic operation. These results indicate that the ion exchange method is promising for industrial lithium isotope separation. (author)

  15. A on-line method for the determination of lead and lead isotope ratios in fresh and saline waters by inductively coupled plasma mass spectrometry

    International Nuclear Information System (INIS)

    Halicz, Ludwik; Lam, J.W.H.; McLaren, J.W.

    1994-01-01

    A previously reported on-line ICP-MS method for the determination of lead and other trace elements in seawater has been re-examined to determine its suitability for the determination of lead isotope ratios ( 206 Pb/ 207 Pb and 207 Pb/ 208 Pb) in fresh and saline natural waters. A detection limit of 0.9 ng/1 for total lead (for a 5 ml sample) was achieved. Precision of isotope ratio data was 0.2-0.3% RSD at a Pb concentration of 1 μg/l, and was still better than 2% at concentrations of only 10-40 ng/1 in seawater certified reference materials (CRMs). For all three natural water CRMs examined, measured precision was very close to the limit predicted by counting statistics. (Author)

  16. Isotope separation by selective dissociation of trifluoromethane with an infrared laser

    International Nuclear Information System (INIS)

    Hartford, A.J.

    1982-01-01

    A process for obtaining compounds enriched in a desired isotope of an element selected from hydrogen and carbon comprises exposing subatmospheric pressure gaseous trifluoromethane containing said desired isotope and one or more other isotopes of the same element to infrared laser radiation of a predetermined frequency, which selectively dissociates trifluoromethane molecules containing said desired isotope and separating the resulting dissociation product enriched in said desired isotope from the remainder of the gas. The term 'trifluoromethane' (TFM) refers to a mixture of CF 3 H and CF 3 D, the latter constituting about 0.015 percent of the total. TFM is irradiated with a CO 2 laser at an appropriate infrared wavelength

  17. Isotope separation process by transfer of vibrational energy

    International Nuclear Information System (INIS)

    Angelie, C.; Cauchetier, M.; Paris, J.

    1983-01-01

    This process consists in exciting A molecules by absorption of a pulsed light beam, then in exciting until their dissociation X molecules, present in several isotopic forms, by a vibrational transfer between the A molecules and the X molecules, the A molecules having a dissociation energy greater than that of the X molecules, the duration and energy of the light pulses being such that the absorption time by the A molecules is less than the excitation time of the X molecules and the temperature conditions such that the thermal width of the vibration rays is at the most near the isotopic difference between the resonance rays of the two isotopic varieties [fr

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

    International Nuclear Information System (INIS)

    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 ( 205 Tl to 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

  19. Determination of lycopene in food by on-line SFE coupled to HPLC using a single monolithic column for trapping and separation

    Czech Academy of Sciences Publication Activity Database

    Pól, Jaroslav; Hyötyläinen, T.; Ranta-Aho, O.; Riekkola, M. L.

    2004-01-01

    Roč. 1052, 1-2 (2004), s. 25-31 ISSN 0021-9673 R&D Projects: GA AV ČR KJB4031405 Grant - others:Academy of Finland Projects(FI) 48867; Academy of Finland Projects(FI) 52746 Institutional research plan: CEZ:AV0Z4031919 Keywords : lycopene * on-line SFE-LC * supercritical fluid extraction Subject RIV: CB - Analytical Chemistry, Separation Impact factor: 3.359, year: 2004

  20. Characteristics of water isotopes and hydrograph separation during ...

    Indian Academy of Sciences (India)

    2College of Geography and Environmental Science, Northwest Normal University, Lanzhou 730070, ... During 2013, a water-isotope source apportionment study was conducted during ..... in the Chilean Andes II: Qualitative and quantitative.

  1. Element for separating gaseous isotopes into at least two fractions and with a separating basket consisting of several separating elements

    International Nuclear Information System (INIS)

    Grossstuck, W.; Schafer, R.

    1985-01-01

    A separating element for gaseous isotopes into two fractions, and consisting of several elongated separating chips with a row of entry openings for the process gas at one side of the chips and a row of exit openings for the heavy fraction at the other side of the chips, with exit openings for the light fraction at the edges of the chips, and of two tubes holding the chips and having at least one chamber, with said tubes being connected by means of connecting elements, and equipped with entry and exit openings on their contact surfaces, with said entry and exit openings arranged in rows in a longitudinal direction of the chips, and for simplifying of installation and construction, this invention provides that the chips are arranged in a longitudinal direction to the tubes, with their sides abutting directly against the smooth contact surfaces of the tubes, and whereby the connecting elements are positioned in one row in the center of the two tubes

  2. Parameter study on Japanese proposal of ITER hydrogen isotope separation system

    International Nuclear Information System (INIS)

    Yoshida, Hiroshi; Enoeda, Mikio; Tanaka, Shigeru; Ohokawa, Yoshinao; Ohara, Atsushi; Nagakura, Masaaki; Naito, Taisei; Nagashima, Kazuhiro.

    1991-01-01

    As part of Japanese design contribution in the ITER activity, conceptual design of an entire ITER tritium system and their safety analysis have been carried out through the three-year period since 1988. The tritium system includes the following subsystems; - Fuelling (gas puffing and pellet injection) subsystem, - Torus vacuum pumping subsystem, - Plasma exhaust gas purification subsystem, - Hydrogen isotope separation subsystem, - NBI gas processing subsystem, - Blanket tritium recovery subsystem, - Tritiated water processing subsystem, - Tritium safety subsystem. Hydrogen isotope separation system is a key subsystem in the ITER tritium system because it is connected to all above subsystems. This report describes an analytical study on the Japanese concept of hydrogen isotope separation system. (author)

  3. A non-conventional isotope separation cascade without any mixing: net cascade

    International Nuclear Information System (INIS)

    Zeng Shi; Jiang Dongjun; Ying Zhengen

    2012-01-01

    A component has different concentrations in the incoming flows at a confluent point in all existing isotope separations cascades for multi-component isotope separation and mixing is inevitable, which results in deterioration of separation performance of the separation cascade. However, realization of no-mixing at a confluent point is impossible with a conventional cascade. A non-conventional isotope separation cascade, net cascade, is found to be able to realize no mixings for all components at confluent points, and its concept is further developed here. No-mixing is fulfilled by requiring symmetrical separation of two specified key components at every stage, and the procedure of realizing no-mixing is presented in detail. Some properties of net cascade are investigated preliminarily, and the results demonstrated the no-mixing property is indeed realized. Net cascade is the only separation cascade that so far possesses the no-mixing property. (authors)

  4. Chromatographic separation process with pellicular ion exchange resins that can be used for ion or isotope separation and resins used in this process

    International Nuclear Information System (INIS)

    Carles, M.; Neige, R.; Niemann, C.; Michel, A.; Bert, M.; Bodrero, S.; Guyot, A.

    1989-01-01

    For separation of uranium, boron or nitrogen isotopes, an isotopic exchange is carried out betwen an isotope fixed on an ion exchange resin and another isotope of the same element in the liquid phase contacting the resin. Pellicular resins are used comprising composite particulates with an inert polymeric core and a surface layer with ion exchange groups [fr

  5. Separation and sampling technique of light element isotopes by chemical exchange process

    International Nuclear Information System (INIS)

    Kato, Shunsaku; Oi, Kenta; Takagi, Norio; Hirotsu, Takafumi; Kano, Hirofumi; Sonoda, Akinari; Makita, Yoji

    2000-01-01

    Lithium and boron isotope separation technique were studied. Granulation of lithium isotope separation agent was carried out by cure covering in solution. Separation of lithium isotope was stepped up by ammonium carbonate used as elusion agent. Styrene and ester resin derived three kinds of agents such as 2-amino-1, 3-propanediol (1, 3-PD), 2-amino-2-methyl-1, 3-propanediol (Me-1,3-PD) and tris(2-hydroxyethyl)amine (Tris) were used as absorbent.The ester resin with Tris showed larger amount of adsorption (1.4 mmol/g) than other resins. However, all resins with agent indicated more large adsorption volume of boron than the objective value (0.5 mmol/g). Large isotope shift was shown by the unsymmetrical vibration mode of lithium ion on the basis of quantum chemical calculation of isotope effect on dehydration of hydrated lithium ion. (S.Y.)

  6. Bicarbonate adsorption band of the chromatography for carbon isotope separation using anion exchangers

    International Nuclear Information System (INIS)

    Takeda, Kunihiko; Obanawa, Heiichiro; Hata, Masahisa; Sato, Katsuya

    1985-01-01

    The equilibria of bicarbonate ion between two phases were studied for the carbon isotope separation using anion exchangers. The condition of the formation of a bicarbonate adsorption band was quantitatively discussed. The formation of the adsorption band depends on the difference of S-potential which is the sum of the standard redection chemical potentials and L-potential which is the sum of the reduction chemical potential. The isotopic separation factor observed was about 1.012, independent of the concentrations of acid and alkali in the solutions. The isotopic separation factor was considered to be determined by the reaction of bicarbonate ion on anion exchangers and carbon dioxide dissolved in solutions. The enriched carbon isotope whose isotopic abundance ratio ( 13 C/ 12 C) was 1.258 was obtained with the column packed with anion exchangers. (author)

  7. Laser-induced separation of hydrogen isotopes in the liquid phase

    International Nuclear Information System (INIS)

    Beattie, W.; Freund, S.; Holland, R.; Maier, W.

    1980-01-01

    A process for separating hydrogen isotopes which comprises (A) forming a liquid phase of hydrogen-bearing feedstock compound at a temperature at which the spectral features of the feedstock compound are narrow enough or the absorption edges sharp enough to permit spectral features corresponding to the different hydrogen isotopes to be separated to be distinguished, (B) irradiating the liquid phase at said temperature with monochromatic radiation of a first wavelength which selectively or at least preferentially excites those molecules of said feedstock compound containing a first hydrogen isotope, and (C) subjecting the excited molecules to physical or chemical processes or a combination thereof whereby said first hydrogen isotope contained in said excited molecules is separated from other hydrogen isotopes contained in the unexcited molecules in said liquid phase

  8. On-line hydrogen-isotope measurements of organic samples using elemental chromium: An extension for high temperature elemental-analyzer techniques

    Science.gov (United States)

    Gehre, Matthias; Renpenning, Julian; Gilevska, Tetyana; Qi, Haiping; Coplen, Tyler B.; Meijer, Harro A.J.; Brand, Willi A.; Schimmelmann, Arndt

    2015-01-01

    The high temperature conversion (HTC) technique using an elemental analyzer with a glassy carbon tube and filling (temperature conversion/elemental analysis, TC/EA) is a widely used method for hydrogen isotopic analysis of water and many solid and liquid organic samples with analysis by isotope-ratio mass spectrometry (IRMS). However, the TC/EA IRMS method may produce inaccurate δ2H results, with values deviating by more than 20 mUr (milliurey = 0.001 = 1‰) from the true value for some materials. We show that a single-oven, chromium-filled elemental analyzer coupled to an IRMS substantially improves the measurement quality and reliability for hydrogen isotopic compositions of organic substances (Cr-EA method). Hot chromium maximizes the yield of molecular hydrogen in a helium carrier gas by irreversibly and quantitatively scavenging all reactive elements except hydrogen. In contrast, under TC/EA conditions, heteroelements like nitrogen or chlorine (and other halogens) can form hydrogen cyanide (HCN) or hydrogen chloride (HCl) and this can cause isotopic fractionation. The Cr-EA technique thus expands the analytical possibilities for on-line hydrogen-isotope measurements of organic samples significantly. This method yielded reproducibility values (1-sigma) for δ2H measurements on water and caffeine samples of better than 1.0 and 0.5 mUr, respectively. To overcome handling problems with water as the principal calibration anchor for hydrogen isotopic measurements, we have employed an effective and simple strategy using reference waters or other liquids sealed in silver-tube segments. These crimped silver tubes can be employed in both the Cr-EA and TC/EA techniques. They simplify considerably the normalization of hydrogen-isotope measurement data to the VSMOW-SLAP (Vienna Standard Mean Ocean Water-Standard Light Antarctic Precipitation) scale, and their use improves accuracy of the data by eliminating evaporative loss and associated isotopic fractionation while

  9. On-line hydrogen-isotope measurements of organic samples using elemental chromium: an extension for high temperature elemental-analyzer techniques.

    Science.gov (United States)

    Gehre, Matthias; Renpenning, Julian; Gilevska, Tetyana; Qi, Haiping; Coplen, Tyler B; Meijer, Harro A J; Brand, Willi A; Schimmelmann, Arndt

    2015-01-01

    The high temperature conversion (HTC) technique using an elemental analyzer with a glassy carbon tube and filling (temperature conversion/elemental analysis, TC/EA) is a widely used method for hydrogen isotopic analysis of water and many solid and liquid organic samples with analysis by isotope-ratio mass spectrometry (IRMS). However, the TC/EA IRMS method may produce inaccurate δ(2)H results, with values deviating by more than 20 mUr (milliurey = 0.001 = 1‰) from the true value for some materials. We show that a single-oven, chromium-filled elemental analyzer coupled to an IRMS substantially improves the measurement quality and reliability for hydrogen isotopic compositions of organic substances (Cr-EA method). Hot chromium maximizes the yield of molecular hydrogen in a helium carrier gas by irreversibly and quantitatively scavenging all reactive elements except hydrogen. In contrast, under TC/EA conditions, heteroelements like nitrogen or chlorine (and other halogens) can form hydrogen cyanide (HCN) or hydrogen chloride (HCl) and this can cause isotopic fractionation. The Cr-EA technique thus expands the analytical possibilities for on-line hydrogen-isotope measurements of organic samples significantly. This method yielded reproducibility values (1-sigma) for δ(2)H measurements on water and caffeine samples of better than 1.0 and 0.5 mUr, respectively. To overcome handling problems with water as the principal calibration anchor for hydrogen isotopic measurements, we have employed an effective and simple strategy using reference waters or other liquids sealed in silver-tube segments. These crimped silver tubes can be employed in both the Cr-EA and TC/EA techniques. They simplify considerably the normalization of hydrogen-isotope measurement data to the VSMOW-SLAP (Vienna Standard Mean Ocean Water-Standard Light Antarctic Precipitation) scale, and their use improves accuracy of the data by eliminating evaporative loss and associated isotopic fractionation while

  10. Determination of the separation factor of uranium isotopes by gaseous diffusion

    International Nuclear Information System (INIS)

    Bilous, O.; Counas, G.

    1958-01-01

    A 12-stage pilot separation cascade with a low output has been constructed to measure the separation factor of uranium isotopes by gaseous diffusion. The report describes some of the separation results obtained, and also provides information on the time necessary for equilibrium to be established and on the influence of various perturbations on the pressure profile in the cascade. (author) [fr

  11. Performance of the multiple target He/PbI sub 2 aerosol jet system for mass separation of neutron-deficient actinide isotopes

    CERN Document Server

    Ichikawa, S; Asai, M; Haba, H; Sakama, M; Kojima, Y; Shibata, M; Nagame, Y; Oura, Y; Kawade, K

    2002-01-01

    A multiple target He/PbI sub 2 aerosol jet system coupled with a thermal ion source was installed in the isotope separator on line (JAERI-ISOL) at the JAERI tandem accelerator facility. The neutron-deficient americium and curium isotopes produced in the sup 2 sup 3 sup 3 sup , sup 2 sup 3 sup 5 U( sup 6 Li, xn) and sup 2 sup 3 sup 7 Np( sup 6 Li, xn) reactions were successfully mass-separated and the overall efficiency including the ionization of Am atoms was evaluated to be 0.3-0.4%. The identification of a new isotope sup 2 sup 3 sup 7 Cm with the present system is reported.

  12. The ISOLDE experimental hall, wth the isotope separator in the upper left corner.

    CERN Multimedia

    CERN PhotoLab

    1969-01-01

    Beam tubes branch out from a switchyard, which by electrostatic deflectors direct beams of short-lived isotopes to various spectroscopic equipment. From left to right, Rudi Stoeckli at the separator control panel, Gilbert Droz and Henri Bersinger.

  13. Studies on separation of lithium isotopes by solvent extraction: Pt.1

    International Nuclear Information System (INIS)

    Chen Yaohuan; Yan Jinying; Wu Fubing

    1987-01-01

    The separation effects of lithium isotopes on the extraction with Sudan I(1-phenylazo-2-naphthol)-neutral ligand synergetic extraction systems are reported in this paper. Different separation effects are observed when different kinds of neutral ligands are used. Among them, the separation coefficient (α) of Sudan I-TOPO-xylene/LiCl-LiOH is found to be 1.009 ± 0.001. The heavy isotope 7 Li is enriched in the organic phase. The contributions of different structural chelating agents, synergetic agents and diluents to the separation effect are discussed. It is shown that the chelating agent played an important role in the separation effect, and the synergetic agent also exhibited obvious effect, while the shift of diluent didn't affect the separation coefficient significantly. The rates of extraction and isotope exchange equilibrium are high and these systems are shown to be diffusion-controlled ones

  14. Method for separating the isotopes of a chemical element

    International Nuclear Information System (INIS)

    Devienne, F.M.

    1977-01-01

    A beam of positive or negative primary ions of at least one compound of a chemical element is accelerated in order to pass through collision boxes placed in series. As a result of inelastic collisions of the ions with the molecules of a neutral target gas within each collision box, a given percentage of primary ions is dissociated into at least two fragments, one of which is a secondary ion in the form of at least two isotopic species. The collision boxes are brought to a potential V 2 so as to trap preferentially one isotopic species which is condensed within each box. 15 claims, 4 figures

  15. A Monte Carlo simulation of neon isotope separation in a DC discharge through a narrow capillary

    International Nuclear Information System (INIS)

    Niroshi Akatsuka; Masaaki Suzuki

    1999-01-01

    A numerical simulation was undertaken on the neon isotope separation in a DC arc discharge through a narrow capillary. The mass transport phenomenon of neutral particles as well as ions was treated by the direct simulation Monte Carlo (DSMC) method. The numerical results qualitatively agreed with existing experimental ones concerning not only the isotope separation phenomena, but also the pressure difference between the region of the anode and that of the cathode [ru

  16. Separation and enrichment of isotopes using laser photochemistry - fundamentals and prospectives

    International Nuclear Information System (INIS)

    Guesten, H.

    1978-01-01

    Basic knowledge is summed up on isotope separation by laser photochemistry. The principal prerequisites are explained of the application of atomic and molecular spectroscopy for this purpose. Practical examples are given of isotope separation of uranium, nitrogen, chlorine, carbon, sulfur, and molybdenum showing the application of two basic techniques, i.e., of gradual atom photoionization or gradual molecule photodissociation and of selective photochemical reactions. (L.K.)

  17. Utility of reversed phase high performance liquid chromatography for on-line yield determination of radiochemical separations: Studies with cobalt

    International Nuclear Information System (INIS)

    Subramanian, S.; Woittiez, J.R.W.

    1993-01-01

    This article indicates the potentials of high performance liquid chromatography (HPLC) as a radiochemical technique for multielement separation of neutron irradiated samples. The focus lies on the convenience to use the detector signal of the eluted components to indicate the chemical yield of the analyte, which has often proved to be a crucial step in radiochemical separations. Two signals have been utilized. The UV signal of the metal-ligand complexes separated by reversed phase HPLC and the radioactive response as a result of sample irradiation of carrier-tracer addition. Change in ratio is discussed between the two signals, if any, for a specific sample. Losses of metal as much as 65% were simulated and corrected using the individual UV response. The method promises improved accuracy for elemental analysis despite losses suffered during the various chemical steps. The procedure omits the necessity of additional analytical steps for yield determination. The present article aims at the chromatographic part of the study. Cobalt as cobalt diethyldithiocarbamate has been used to demonstrate the viability of the concept. The separation was developed on c C18 reverse phase analytical column and optimized on a semi preparative one

  18. Vacuum-arc plasma centrifuge applied to stable isotope separation

    International Nuclear Information System (INIS)

    Del Bosco, E.

    1989-09-01

    This work describes the results of a vacuum-arc plasma centrifuge experiment. A plasma centrifuge is an apparatus where a plasma column is produced due to the interaction of an electric current with an externally applied magnetic field, sup(→)J x sup(→)B. Among the applications of a rotating plasma, this work deals particularly with its utilization in an isotope enrichment device. The main characteristics of the plasma produced in this experiment are presented, with special attention to the plasma column rotation and the isotope enrichment. The analysis of the results is performed using a fluid model for a completely ionized rigid body rotating plasma column in steady state equilibrium. The main results are: a) rotation frequency of the plasma column in the range 2 x 10 sup(4) to 3 x 10 sup(5) rad/s; b) enrichment of 10 to 30% for the magnesium isotopes, and of 290 to 490% for the carbon 13 isotope; c) rigid body rotation of the plasma column only for radii smaller than the characteristic radius of the plasma column. re; d) linear dependence of the rotation frequency upon the magnetic field strength only for r < re; e) existence of an optimum value of the magnetic field for maximum enrichment; and f) dependence of the rotation frequency upon the inverse of the atomic mass. (author)

  19. LLNL medical and industrial laser isotope separation: large volume, low cost production through advanced laser technologies

    International Nuclear Information System (INIS)

    Comaskey, B.; Scheibner, K. F.; Shaw, M.; Wilder, J.

    1998-01-01

    The goal of this LDRD project was to demonstrate the technical and economical feasibility of applying laser isotope separation technology to the commercial enrichment (>lkg/y) of stable isotopes. A successful demonstration would well position the laboratory to make a credible case for the creation of an ongoing medical and industrial isotope production and development program at LLNL. Such a program would establish LLNL as a center for advanced medical isotope production, successfully leveraging previous LLNL Research and Development hardware, facilities, and knowledge

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

    Science.gov (United States)

    Watkins, James M.; DePaolo, Donald J.; Ryerson, Frederick J.; Peterson, Brook T.

    2011-06-01

    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 2Si 2O 8; denoted AN), albite (NaAlSi 3O 8; denoted AB), and diopside (CaMgSi 2O 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 Ca/ D Si ≈ 20 and the efficiency of isotope separation for Ca is much greater than in natural liquid experiments where D Ca/ D Si ≈ 1. In the AB-DI experiment, D Ca/ D 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 Mg/ D 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 Ca) to the diffusivity of silicon ( D 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 cation/ D Si. Cations diffusing in aqueous solutions display a similar relationship

  1. Apparatus for isotopic separation using a high-frequency wave and coherent radiation

    International Nuclear Information System (INIS)

    Mourier, G.

    1983-11-01

    The purpose of the present invention is an apparatus for industrial separation of isotopes, using a high-frequency electromagnetic field and coherent radiation such as that from a laser. Separation of isotopes by isotopically selective ionization, followed by entrainment of the ions by means of a magnetic field, is known. The selective ionization operation can be carried out in two consecutive stages: excitation of the chosen isotope, from the ground energy state to a specified excited level, near ionization; the energy required for this first stage can be supplied by means of a laser, the laser radiation being characterized for high power and well-defined frequency; this stage offers the advantage of being easily made isotopically selective; then ionization of the excited atoms by means of supplying relatively weak energy which should be insufficient to ionize the nonexcited ions; this second stage can also be carried out by means of a laser

  2. The study of multicomponent separation of Xe isotope by centrifugal method

    International Nuclear Information System (INIS)

    Jinyan Wu; Fu Zhuge

    1996-01-01

    The element Xe has nine isotopes in nature, the separation performance of each component mutually affects the others, so the binary separation theory can't be employed to study the multicomponent separation. Especially, when the molecular wight of a certain component is in the middle of its isotope components, the effect of the others on this component must be considered. In this paper, first, the multicomponent separation of Xe isotopes in a gas centrifuge is studied, with the consideration of the effect of the concentration on the diffusion coefficient and average molecular weight. The multicomponent diffusion equations are solved by the finite difference method. Second, the enrichment of Xe isotopes in a cascade is studied. On the basis of the study of a gas centrifuge, the simplified separation equations of a gas centrifuge for cascade calculation are obtained. Furthermore, the complete equations of the cascade separation are established according to the conservation of mass of each component and solved by a numerical method. The study of this paper can be extended for other isotope separation calculations. (author)

  3. Device for the separation of isotopic uranium compounds

    International Nuclear Information System (INIS)

    Niemann, H.J.; Sprehe, J.

    1985-01-01

    The UF6-isotopes selectively converted by low radiation are contained in a beam. The boundary region of this gas beam hits a target which is oriented in vertical angle to the gas beam and exerts a compression shock on it. This peel border leads to diversion of the reaction products of light mass, whereas the heavy mass, products flow into a receiver. (orig./PW)

  4. Lithium isotope separation factors of some two-phase equilibrium systems

    International Nuclear Information System (INIS)

    Palko, A.A.; Drury, J.S.; Begun, G.M.

    1976-01-01

    Isotope separation factors of seventeen two-phase equilibrium systems for lithium isotope enrichment have been determined. In all cases, lithium amalgam was used as one of the lithium-containing phases and was equilibrated with an aqueous or organic phase containing a lithium compound. In all systems examined, isotopic exchange was found to be extremely rapid, and 6 Li was concentrated in the amalgam phase. The isotopic separation factor for the LiOH(aqueous) vs Li(amalgam) system has been studied as a function of temperature from -2 to 80 degreeC. The values obtained have been compared with the ''electrolysis'' and exchange separation factors given in the literature. The two-phase systems, LiCl(ethylenediamine) vs Li(amalgam) and LiCl(propylenediamine) vs Li(amalgam), have been studied, and the isotopic separation factors have been determined as functions of the temperature. The factors for the two systems have been found to be substantially the same (within limits of the errors involved) over the temperature range studied (0 to 100 degreeC) as those for the aqueous system. The isotopic separation factors for the seventeen systems have been tabulated, and correlations have been drawn that show the salt and solvent effects upon the values obtained

  5. Pooled versus separate measurements of tree-ring stable isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Dorado Linan, Isabel, E-mail: isabel@gfz-potsdam.de [Universitat de Barcelona, Departament d' Ecologia, Diagonal 645, 08028, Barcelona (Spain); German Centre for Geosciences, Climate Dynamics and Landscape Evolution, Dendro Laboratory, Telegrafenberg, 14473, Potsdam (Germany); Gutierrez, Emilia, E-mail: emgutierrez@ub.edu [Universitat de Barcelona, Departament d' Ecologia, Diagonal 645, 08028, Barcelona (Spain); Helle, Gerhard, E-mail: ghelle@gfz-potsdam.de [German Centre for Geosciences, Climate Dynamics and Landscape Evolution, Dendro Laboratory, Telegrafenberg, 14473, Potsdam (Germany); Heinrich, Ingo, E-mail: heinrich@gfz-potsdam.de [German Centre for Geosciences, Climate Dynamics and Landscape Evolution, Dendro Laboratory, Telegrafenberg, 14473, Potsdam (Germany); Andreu-Hayles, Laia, E-mail: laiandreu@ub.edu [Universitat de Barcelona, Departament d' Ecologia, Diagonal 645, 08028, Barcelona (Spain); Tree-Ring Laboratory, Lamont-Doherty Earth Observatory of Columbia University, Palisades NY (United States); Planells, Octavi, E-mail: leocarpus@hotmail.com [Universitat de Barcelona, Departament d' Ecologia, Diagonal 645, 08028, Barcelona (Spain); Leuenberger, Markus, E-mail: leuenberger@climate.unibe.ch [Climate and Environmental Physics, Physics Institute, University of Bern, Sidlerstrasse 5, 3012 Bern (Switzerland); Oeschger Centre of Climate Change Research, University of Bern, Zaehringerstrasse 25, 3012 Bern (Switzerland); Buerger, Carmen, E-mail: buerger@gfz-potsdam.de [German Centre for Geosciences, Climate Dynamics and Landscape Evolution, Dendro Laboratory, Telegrafenberg, 14473, Potsdam (Germany); Schleser, Gerhard, E-mail: schleser@gfz-potsdam.de [German Centre for Geosciences, Climate Dynamics and Landscape Evolution, Dendro Laboratory, Telegrafenberg, 14473, Potsdam (Germany)

    2011-05-01

    {delta}{sup 13}C and {delta}{sup 18}O of tree rings contain time integrated information about the environmental conditions weighted by seasonal growth dynamics and are well established as sources of palaeoclimatic and ecophysiological data. Annually resolved isotope chronologies are frequently produced by pooling dated growth rings from several trees prior to the isotopic analyses. This procedure has the advantage of saving time and resources, but precludes from defining the isotopic error or statistical uncertainty related to the inter-tree variability. Up to now only a few studies have compared isotope series from pooled tree rings with isotopic measurements from individual trees. We tested whether or not the {delta}{sup 13}C and the {delta}{sup 18}O chronologies derived from pooled and from individual tree rings display significant differences at two locations from the Iberian Peninsula to assess advantages and constraints of both methodologies. The comparisons along the period 1900-2003 reveal a good agreement between pooled chronologies and the two mean master series which were created by averaging raw individual values (Mean) or by generating a mass calibrated mean (MassC). In most of the cases, pooled chronologies show high synchronicity with averaged individual samples at interannual scale but some differences also show up especially when comparing {delta}{sup 18}O decadal to multi-decadal variations. Moreover, differences in the first order autocorrelation among individuals may be obscured by pooling strategies. The lack of replication of pooled chronologies prevents detection of a bias due to a higher mass contribution of one sample but uncertainties associated with the analytical process itself, as sample inhomogeneity, seems to account for the observed differences. - Research Highlights: {yields} Pooled {delta}{sup 13}C and {delta}{sup 18}O chronologies are expected to be similar to the mean. {yields} Empirical pooled chronologies {delta}{sup 13}C and

  6. Pooled versus separate measurements of tree-ring stable isotopes

    International Nuclear Information System (INIS)

    Dorado Linan, Isabel; Gutierrez, Emilia; Helle, Gerhard; Heinrich, Ingo; Andreu-Hayles, Laia; Planells, Octavi; Leuenberger, Markus; Buerger, Carmen; Schleser, Gerhard

    2011-01-01

    δ 13 C and δ 18 O of tree rings contain time integrated information about the environmental conditions weighted by seasonal growth dynamics and are well established as sources of palaeoclimatic and ecophysiological data. Annually resolved isotope chronologies are frequently produced by pooling dated growth rings from several trees prior to the isotopic analyses. This procedure has the advantage of saving time and resources, but precludes from defining the isotopic error or statistical uncertainty related to the inter-tree variability. Up to now only a few studies have compared isotope series from pooled tree rings with isotopic measurements from individual trees. We tested whether or not the δ 13 C and the δ 18 O chronologies derived from pooled and from individual tree rings display significant differences at two locations from the Iberian Peninsula to assess advantages and constraints of both methodologies. The comparisons along the period 1900-2003 reveal a good agreement between pooled chronologies and the two mean master series which were created by averaging raw individual values (Mean) or by generating a mass calibrated mean (MassC). In most of the cases, pooled chronologies show high synchronicity with averaged individual samples at interannual scale but some differences also show up especially when comparing δ 18 O decadal to multi-decadal variations. Moreover, differences in the first order autocorrelation among individuals may be obscured by pooling strategies. The lack of replication of pooled chronologies prevents detection of a bias due to a higher mass contribution of one sample but uncertainties associated with the analytical process itself, as sample inhomogeneity, seems to account for the observed differences. - Research Highlights: → Pooled δ 13 C and δ 18 O chronologies are expected to be similar to the mean. → Empirical pooled chronologies δ 13 C and δ 18 O and the mean show a high synchronicity. → Pooled chronologies differ

  7. ELGA and TOR installations control device to carry out experiments on-line with a mass-separator by the ASNAPP-2 code

    International Nuclear Information System (INIS)

    Arvai, Z.; Guyash, Ya.; Kuznetsov, V.V.; Fominykh, V.I.

    1984-01-01

    The control device of the tor beta-spectrometer with toroidal magnetic field and the ELGA spectrometer with semiconductor detectors for investigation of conversion electrons, positrons, γ- and α-radiations and lifetime of excited states and periods of isotopes half-decay are described. The block-diagram of the measurement processes, algorithm of the ELGA devce operation, control device circuit, and circuit for connection of analog-to-digital converter with the CAMAC dataway, block-diagram of step motor control, and step motor feeding scheme as well as mechanical and electrical characteristics of the step motor are given. The device is used for spectroscopic investigations of short-lived isotopes on the accelerator proton beam with mass separator

  8. Recent progress of in-flight separators and rare isotope beam production

    Energy Technology Data Exchange (ETDEWEB)

    Kubo, Toshiyuki, E-mail: kubo@ribf.riken.jp

    2016-06-01

    New-generation in-flight separators are being developed worldwide, including the Super-FRS separator at the GSI Facility for Antiproton and Ion Research (FAIR), the ARIS separator at the Michigan State University (MSU) Facility for Rare Isotopes Beams (FRIB), and the BigRIPS separator at the RIKEN RI Beam Factory (RIBF), each of which is aimed at expanding the frontiers of rare isotope (RI) production and advancing experimental studies on exotic nuclei far from stability. Here, the recent progress of in-flight separators is reviewed, focusing on the advanced features of these three representative separators. The RI beam production that we have conducted using the BigRIPS separator at RIKEN RIBF is also outlined.

  9. Sb(III) and Sb(V) separation and analytical speciation by a continuous tandem on-line separation device in connection with inductively coupled plasma atomic emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Menendez Garcia, A. [Oviedo Univ. (Spain). Dept. of Phys. and Anal. Chem.; Perez Rodriguez, M.C. [Oviedo Univ. (Spain). Dept. of Phys. and Anal. Chem.; Sanchez Uria, J.F. [Oviedo Univ. (Spain). Dept. of Phys. and Anal. Chem.; Sanz-Medel, A. [Oviedo Univ. (Spain). Dept. of Phys. and Anal. Chem.

    1995-09-01

    A sensitive, precise and automated non-chromatographic method for Sb(III) and Sb(V) analytical speciation based on a continuous tandem on-line separation device in connection with inductively coupled plasma-atomic emission (ICP-AES) detection is proposed. Two on-line successive separation steps are included into this method: a continuous liquid-liquid extraction of Sb(III) with ammonium pyrrolidine dithiocarbamate (APDC) into methylisobuthylketone (MIBK), followed by direct stibine generation from the organic phase. Both separation steps are carried out in a continuous mode and on-line with the ICP-AES detector. Optimization of experimental conditions for the tandem separation and ICP-AES detection are investigated in detail. Detection limits for Sb(III) were 3 ng.mL{sup -1} and for Sb(V) 8 ng.mL{sup -1}. Precisions observed are in the range {+-} 5%. The proposed methodology has been applied to Sb(III) and Sb(V) speciation in sea-water samples. (orig.)

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

    International Nuclear Information System (INIS)

    Zisman, M.S.

    1982-01-01

    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

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

    Energy Technology Data Exchange (ETDEWEB)

    Zisman, M.S.

    1982-01-01

    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.

  12. Light induced drift: a possible mechanism of separation of isotopes by laser excitation

    International Nuclear Information System (INIS)

    Biswas, D.J.; Nilaya, J.P.; Venkatramani, N.

    2003-02-01

    A comprehensive review of the literature on the effect of light induced drift and its exploitation in the separation of isotopes, both in atomic and molecular forms, is presented. An experimental scheme based on this effect to separate S 33 , with a natural abundance of ∼0.76%, from SF 6 has also been worked out. (author)

  13. Electromagnetic separation of stable isotopes at the Institute of Atomic Energy, Academia Sinica

    International Nuclear Information System (INIS)

    Hua, M.; Li, G.; Su, S.; Mao, N.; Lu, H.

    1981-01-01

    For almost 20 years the Institute of Atomic Energy, Academia Sinica has been separating stable isotopes of the elements by electromagnetic separators and supplying these materials to research work in many fields of our country. In this article we shall attempt to outline the growth of the effort and describe the present situation. (orig.)

  14. The instability of molecules in laser field and isotope separation

    International Nuclear Information System (INIS)

    Li, K.

    1981-01-01

    In the present paper the nonlinear differential equation describing the selective decomposition of a molecule as an unimolecular reaction has be deduced from the usual time dependent semi-classical Schroedinger equation. The selective conditions for the instability of a molecule are discussed. The thresholds of the required laser intensities for ICl and HCl diatomic molecules are estimated respectively, where on type of isotope molecules ought to be decomposed for hundred per cent in a laser pulse for different pulse widths. And possibly selective decomposition of the molecule without permanent dipole moment by Raman process is also discussed briefly. (orig.)

  15. Isotopic separation of nitrogen 15. Influence of the gaseous phase composition

    International Nuclear Information System (INIS)

    Lacoste, Germain; Routie, Rene; Mahenc, Jean

    1977-01-01

    A study has been made on the gas phase composition effect on the isotopic separation of nitrogen 15 for the two HNO 3 -NO and N 2 O 3 -NO systems. It was shown that the changes in composition of the gas phases could account for the increase in the overall separation; most accuracy, measurements of isotopic concentration along the separation column and of total enrichment exhibit how important are the reactions of oxydo-reduction between the two phases in such process [fr

  16. Electromagnetic separator for light and middle isotope elements; Separateur electromagnetique pour les isotopes d'elements legers et moyens

    Energy Technology Data Exchange (ETDEWEB)

    Bernas, R [Commissariat a l' Energie Atomique, Lab. du Fort de Chatillon, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1952-07-01

    We describe a separator of isotope with a 60 deg magnetic sector that permits, thanks to a process of neutralization of the space charge, to use efficiently intense ion beams. The ion source for solid is essentially constituted by a discharge of hot cathode in a magnetic field and provides an ion beam focused of more than 10 mA. The result of the first separations (Zn, Sb, Hg) indicates that the isotopes of various elements can be obtained in quantities varying from 10 to 100 mg/24 hours. (author) [French] 0n decrit un separateur d'isotope a secteur magnetique de 60 deg qui permet, grace a un procede de neutralisation de la charge d'espace, d'utiliser efficacement des faisceaux d'ions intenses. La source d'ions pour solide est essentiellement constituee par une decharge a cathode chaude dans un champ magnetique et fournit un faisceau d'ion focalises de plus de 10 mA. Le resultat des premieres separations (Zn, Sb, Hg) indique que les isotopes de divers elements peuvent etre obtenus en quantites variant de 10 a 100 mg/24 heures. (auteur)

  17. Study on decay of 118Xe and 119Xe by means of mass-separator on-line with a synchrocyclotron

    International Nuclear Information System (INIS)

    Berlovich, Eh.E.; Batist, L.Kh.; Blinnikov, Yu.S.

    1976-01-01

    The decay of sup(118, 119)Xe isotopes has been investigated. An experimental device involving a mass-separator operating in line with a synchrocyclotron is briefly outlined. The elements to be investigated were isolated from a proton-irradiated target by the 'on-beam-chemistry' methods and transferred into the mass-separator ion source. The Xe separated ions are transported to detectors in an experimental ha ll. The energies and relative γ ray intensities of 118 Xe → 118 J and of 119 Xe → 119 J decays ar presented. The error of the γ ray energy determination does not exceed 0.6 keV. Obtained are the periods of half-life: for 118 Xe - (3.8+-0.9) min, for 119 Xe - (5.8+-0.3) min. The decay scheme for 119 Xe is made up. The scheme of 119 Xe levels is well inscribed into the general systematics of the J odd isotope levels. On the basis of obtained and known data the spin values are described to the 119 J levels

  18. Molecular modeling study of lithium isotopic separation by crown-ethers in ethanol

    International Nuclear Information System (INIS)

    Dehez, F.

    2002-01-01

    The isotopic separation of lithium ion isotopes is studied at the CEA in Pierrelatte using a liquid chromatography technique. Exchange systems are composed by crown-ethers grafted on silica (12C4, 15C5, B15C5, DB15C5, 18C6, B18C6). Lithium is introduced as a salt melted in ethanol. This work concerns the theoretical study of lithium isotopic exchange reactions with those systems. After a brief presentation of isotope separation techniques and isotopic effects (Chap.I), we describe the methods of theoretical chemistry used in this work (Chap. II). In chapter III, we test AM1 and PM3 semi-empirical methods for the treatment of Li + /crown-ether species. Then, we calculate isotopic separation factors via ab initio and semi-empirical calculations for the exchange reactions in vacuum. The different crown-ethers are considered with and without graftings arms. Studies of exchange reactions in ethanol are presented in chapter IV. First, each species of the reaction are solvated by a few ethanol molecules. Isotopic separation factors calculated show a large effect of the solvent on the exchange reaction. The effect of the grafting arm has been investigated using hybrid quantum mechanics/molecular mechanics (QM/MM) molecular dynamics for species with the 12C4. Trajectories have been generated successively with 7 Li and 6 Li. Atomic velocity autocorrelation functions have allowed the access to vibrational frequencies necessary to calculate isotopic separation factors. The last chapter is devoted to methodological developments made during this Ph.D. We propose an approach to treat long range electrostatic interactions in hybrid QM/MM method, relying on a lattice summation technique. (author) [fr

  19. Application and recovery of ionic liquids in the preparative separation of four flavonoids from Rhodiola rosea by on-line three-dimensional liquid chromatography.

    Science.gov (United States)

    Ma, Shufeng; Hu, Liming; Ma, Chaoyang; Lv, Wenping; Wang, Hongxin

    2014-09-01

    A novel on-line three-dimensional liquid chromatography method was developed to separate four main flavonoids from Rhodiola rosea. Ethyl acetate/0.5 mol/L ionic liquid 1-butyl-3-methylimidazolium chloride aqueous solution was selected as the solvent system. In the first-dimension separation, the target flavonoids were entrapped and subsequently desorbed into the second-dimension high-speed countercurrent chromatographic column for separation. In the third-dimension chromatography, the residual ionic liquid in the four separated flavonoids was removed and the used ionic liquid was recovered. As a result, 35.1 mg of compound 1, 20.4 mg of compound 2, 8.5 mg of compound 3, and 10.6 mg of compound 4 were obtained from 1.53 g R. rosea extract. They were identified as rhodiosin, rhodionin, herbacetin, and kaempferol, respectively. The recovery of ionic liquid reached 99.1% of the initial amount. The results showed that this method is a powerful technology for the separation of R. rosea flavonoids and that the ionic-liquid-based solvent system has advantages over traditional solvent systems in renewable and environmentally friendly properties. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  20. Development and application of an on-line sequential injection system for the separation of artificial and natural radionuclides in environmental samples

    International Nuclear Information System (INIS)

    Kim, C.-K.; Sansone, U.; Martin, P.; Kim, C.-S.

    2007-02-01

    The Chemistry Unit of the Physics, Chemistry and Instrumentation Laboratory in the IAEA's Seibersdorf Laboratory in Austria, has the programmatic responsibility to provide assistance to Member State laboratories in maintaining and improving the reliability of analytical measurement results, both in trace element and radionuclide determinations. This is accomplished through the provision of reference materials of terrestrial origin, validated analytical procedures, training in the implementation of internal quality control, and through the evaluation of measurement performance by organization of worldwide and regional interlaboratory comparison exercises. In this framework an on-line sequential injection (SI) system was developed, which can be widely used for the separation and preconcentration of target analytes from diverse environmental samples. The system enables the separation time to be shortened by maintaining a constant flow rate of solution and by avoiding clogging or bubbling in a chromatographic column. The SI system was successfully applied to the separation of Pu in IAEA reference material (IAEA Soil-6) and to the sequential separation of 210 Po and 210 Pb in phosphogypsum candidate reference material. The replicate analysis results of Pu in IAEA reference material (Soil-6) obtained with the SI system are in good agreement with the recommended value within 5% of standard deviation. The SI system enabled a halving in the separation time required for of radionuclides

  1. Optimization of on-line hydrogen stable isotope ratio measurements of halogen- and sulfur-bearing organic compounds using elemental analyzer-chromium/high-temperature conversion isotope ratio mass spectrometry (EA-Cr/HTC-IRMS).

    Science.gov (United States)

    Gehre, Matthias; Renpenning, Julian; Geilmann, Heike; Qi, Haiping; Coplen, Tyler B; Kümmel, Steffen; Ivdra, Natalija; Brand, Willi A; Schimmelmann, Arndt

    2017-03-30

    Accurate hydrogen isotopic analysis of halogen- and sulfur-bearing organics has not been possible with traditional high-temperature conversion (HTC) because the formation of hydrogen-bearing reaction products other than molecular hydrogen (H 2 ) is responsible for non-quantitative H 2 yields and possible hydrogen isotopic fractionation. Our previously introduced, new chromium-based EA-Cr/HTC-IRMS (Elemental Analyzer-Chromium/High-Temperature Conversion Isotope Ratio Mass Spectrometry) technique focused primarily on nitrogen-bearing compounds. Several technical and analytical issues concerning halogen- and sulfur-bearing samples, however, remained unresolved and required further refinement of the reactor systems. The EA-Cr/HTC reactor was substantially modified for the conversion of halogen- and sulfur-bearing samples. The performance of the novel conversion setup for solid and liquid samples was monitored and optimized using a simultaneously operating dual-detection system of IRMS and ion trap MS. The method with several variants in the reactor, including the addition of manganese metal chips, was evaluated in three laboratories using EA-Cr/HTC-IRMS (on-line method) and compared with traditional uranium-reduction-based conversion combined with manual dual-inlet IRMS analysis (off-line method) in one laboratory. The modified EA-Cr/HTC reactor setup showed an overall H 2 -recovery of more than 96% for all halogen- and sulfur-bearing organic compounds. All results were successfully normalized via two-point calibration with VSMOW-SLAP reference waters. Precise and accurate hydrogen isotopic analysis was achieved for a variety of organics containing F-, Cl-, Br-, I-, and S-bearing heteroelements. The robust nature of the on-line EA-Cr/HTC technique was demonstrated by a series of 196 consecutive measurements with a single reactor filling. The optimized EA-Cr/HTC reactor design can be implemented in existing analytical equipment using commercially available material and

  2. Scaling of rotation and isotope separation in a vacuum-arc centrifuge

    International Nuclear Information System (INIS)

    Prasad, R.R.; Krishnan, M.

    1987-01-01

    Scaling is described of rotation, plasma column size and separation in a vacuum-arc centrifuge. The vacuum-arc centrifuge is a magnetized, fulled ionized, quasineutral column of plasma. The source of plasma is a vacuum-arc discharge between a negatively biased cathode and a grounded mesh anode. Rigid-body rotation, induced by the J x B force, causes radial, centrifugal separation of isotopes in the plasma column. Salient features of a fluid model that provides an understanding of rotation and the concomitant isotope separation in the vacuum-arc centrifuge are described. Scaling of rotation and plasma column size is found be consistent with the model. Measurements of isotope separation, also found to agree with the predictions of the model, are presented. Results of a parametric analysis of isotope separation in such a vacuum-arc centrifuge, using the fluid model and the observed scaling laws, are described. An analysis of the energy cost of separation of the vacuum-arc centrifuge shows that it typically requires only 70 keV/separated atom. (orig.)

  3. Design study of fuel circulating system using Pd alloy membrane isotope separation method

    International Nuclear Information System (INIS)

    Naito, T.; Yamada, T.; Aizawa, T.; Kasahara, T.; Yamanaka, T.

    1981-01-01

    It is expected that the method of permeating through Pd-alloy membrances is effective for isotope separation and the refining of fuel gas. In this paper, the design study of the Fuel Circulating System (FCS) using Pb-alloy membranes is described. The study is mainly focused on the main vacuum, fuel gas refining, isotope separating, and tritium containment systems. In the fuel gas refining system, impurities are effectively removed by using Pd-alloy membranes. For the isotope separation system, the diffusion method through Pd-alloy membranes was adopted. From the standpoint of the safety and economy, a three-stage tritium containment system was adopted to control tritium release to the environment as low as possible. The principal conclusion drawn from the design study was as follows. In the FCS, while cryogenic distillation method appears to be practicable, Pd-alloy membrane method is attractive for isotope separation and the refining of fuel gas. For a large amount of tritium inventory, handling and control technologies should be completed by the experimental evaluation and development of the components and materials used for the FCS. A three-stage containment system was adopted to control tritium release to environment as low as possible. Consideration to prevent tritium escape will be necessary for fuel gas refiners and isotope separators. (Kato, T.)

  4. Boron isotope separation by ion exchange chromatography using weakly basic anion exchange resin

    International Nuclear Information System (INIS)

    Sakuma, Yoichi; Aida, Masao; Okamoto, Makoto; Kakihana, Hidetake

    1980-01-01

    Isotopic plateau displacement chromatography, a useful method for isotope separation is presented. The boric acid band formed in a column of weakly basic anion exchange resin Diaion WA21 can be eluted with pure water. In order to obtain good accumulation of the isotope effect, a series of experiments with different migration length were carried out. The boron-10 enriched part of the boric acid absorbed band was always preceded by the isotopic plateau part, in which the atomic fraction of boron-10 was maintained at its original value. The atomic fraction of boron-10 at the end of the chromatogram increased with migration length, and in the case of 256-m migration, boron-10 was enriched from its original atomic fraction of 19.84 to 91.00%, the separation factor S being constant irrespective of migration length: S = 1.0100 +- 0.0005. (author)

  5. Lithium isotope separation on an ion exchange resin having azacrown ether as an anchor group

    International Nuclear Information System (INIS)

    Kim, D.W.; Jeong, Y.K.; Lee, J.K.; Hong, Ch.P.; Kim, Ch.S.; Jeon, Y.Sh.

    1997-01-01

    As study on the separation of lithium isotopes was carried out with an ion exchange resin having 1,7,13-trioxa-4,10,16-triazacyclooctadecane (N 3 O 3 ) as an anchor group. The lighter isotope, 6 Li concentrated in the resin phase, while the heavier isotope, 7 Li is enriched in the fluid phase. Upon column chromatography [0.6 cm (I. D.) x 20 cm (height) using 1.0M ammonium chloride solution as an eluent, single separation factor, α, 1.068 ( 6 Li/ 7 Li) r esin/( 6 Li/ 7 Li) s olution was obtained by the GLUECKAUF method from the elution curve and isotope ratios. (author)

  6. Principles behind a He-jet system and its application for isotope separation

    International Nuclear Information System (INIS)

    Wollnik, H.

    1976-01-01

    The functioning of a He-jet transport system in explained paying special attention to the use of aerosols. Three applications of such a He-jet for an isotope separation are discussed: the use behind a recoil fission product separator, the transportation of activity into the ion source of a conventional mass separator, and the transportation into an α- or β-recoil time-of-flight spectrometer. (Auth.)

  7. Chemical methods for Sm-Nd separation and its application in isotopic geological dating

    International Nuclear Information System (INIS)

    Guo Qifeng.

    1990-01-01

    Three chemical methods for Sm-Nd separation are mainly desribed: low chromatography of butamone-ammonium thiocyanate for hight concentration Sm and Nd separation, P 240 column chromatography for medium concentration Sm-Nd separation, and pressure ion exchange for low concentration Sm-Nd. The first Sm-Nd synchrone obtained in China with Sm-Nd methods is introduced and Sm-Nd isotopic geological dating in Early Archaean rocks in eastern Hebei has been determined

  8. Method and equipment of separation of gaseous and vaporous materials, particularly isotopes, with separation nozzles

    International Nuclear Information System (INIS)

    Becker, E.W.; Eisenbeiss, G.; Ehrfeld, W.

    1975-01-01

    The invention improves on the already known separation nozzle method by the two following steps: 1) The partial flows produced within the cascade with various shares of additional gas are introduced into the separating nozzle systems in such a manner that with regard to the additional gas, a molar fraction gradient is created which is in the opposite direction to the gradient created by the separation process. 2) The partial flows produced within the cascade with various compositions of the mixture of substances to be separated are introduced into the separating nozzle systems in such a manner that regarding the substances to be separated, a molar fraction gradient is created which is in the same direction as the molar fraction gradient formed by the separation process. Both measures can be separately applied or in combination with one another; flowsheets of the invented cascade circuits and separating nozzle systems are given. (GG/LH) [de

  9. Method to separate deuterium isotopes using ethylene and ethylene dichloride

    International Nuclear Information System (INIS)

    Benson, S.W.

    1979-01-01

    The separation of deuterium by the dissociation of ethylene vinyl chloride, 1,2-dichloro-ethanes or propylene with the help of intensive, matched infrared lasers enables a relatively good yield if operated on a large scale, e.g. in refineries with large through-put. The deuterium from the laser photolysis of ethylene and vinyl chloride is found in the acetylene formed, which has to be separated off and processed. When using dichloroehtane, the deuterium is found in the vinal chloride formed. The methods are briefly described. (UWI) [de

  10. Derivation of basic equations for rigorous dynamic simulation of cryogenic distillation column for hydrogen isotope separation

    International Nuclear Information System (INIS)

    Kinoshita, Masahiro; Naruse, Yuji

    1981-08-01

    The basic equations are derived for rigorous dynamic simulation of cryogenic distillation columns for hydrogen isotope separation. The model accounts for such factors as differences in latent heat of vaporization among the six isotopic species of molecular hydrogen, decay heat of tritium, heat transfer through the column wall and nonideality of the solutions. Provision is also made for simulation of columns with multiple feeds and multiple sidestreams. (author)

  11. Decay of new mass-separated neutron-deficient La and Ce isotopes

    International Nuclear Information System (INIS)

    Genevey, J.; Gizon, A.; Idrissi, N.; Weiss, B.; Beraud, R.; Charvet, A.; Duffait, R.; Emsallem, A.; Meyer, M.; Ollivier, T.; Redon, N.

    1987-01-01

    By use of a He jet system coupled to a Bernas-Nier ion-source, several new mass-separated A = 122 - 127 isotopes reached in heavy ion fusion reactions at SARA have been identified and studied. From experimental decay properties of La isotopes, systematics of low-lying energy levels have been extended for even-even and odd-A barium. New informations on Ce decay schemes are briefly reported

  12. Adaptation of Boynton's mathematical model to hydrogen isotope separation column by cryogenic distillation

    International Nuclear Information System (INIS)

    Kinoshita, Masahiro; Naruse, Yuji

    1981-08-01

    Boynton's mathematical simulation procedure for multi-component distillation calculations has the advantage that the Jacobian matrix is calculated analytically. The purpose of the present study is to adapt this procedure to hydrogen isotope separation columns by cryogenic distillation. The Boynton's model is modified so that the model can incorporate decay heat of tritium, nonideality of the hydrogen isotope solutions, multiple feeds and multiple sidestreams. Basic equations are derived and the mathematical simulation procedure is briefly explained. (author)

  13. Procedure for 40K isotope separation from beam of potassium atoms using optical orientation of atoms and radio-frequency excitation of target isotope

    International Nuclear Information System (INIS)

    Nikitin, A.I.; Velichko, A.M.; Vnukov, A.V.; Mal'tsev, K.K.; Nabiev, Sh.Sh.

    1999-01-01

    The procedure for potassium isotope separation, which is liable to reduce of the prise of the product as compared with the up-to-date prise of the 40 K isotope obtained by means of electromagnetic procedure for isotope separation, is proposed. The scheme assumes the increasing flow of the wanted isotope at the sacrifice of the increasing intensity of atomic beam and the increase of the selectivity of need isotope atoms at the sacrifice of the the reduction in the square of collector profile. The objective is achieved that provide of polarized state of the potassium atoms is produced by optic orientation with circular-polarized light [ru

  14. Laser isotope separation using selective inhibition and encouragement of dimer formation

    International Nuclear Information System (INIS)

    Kivel, B.

    1979-01-01

    Method and apparatus for inhibiting dimer formation of molecules of a selected isotope type in a cooled flow of gas to enhance the effectiveness of mass difference isotope separation techniques are described. Molecules in the flow containing atoms of the selected isotope type are selectively excited by infrared radiation in order to inhibit the formation of dimers and larger clusters of such molecules, while the molecules not containing atoms of the selected, excited type are encouraged to form dimers and higher order aggregates by the cooling of the gaseous flow. The molecules with the excited isotope will predominate in monomers and will constitute the enriched product stream, while the aggregated group comprising molecules having the unexcited isotope will predominate in dimers and larger clusters of molecules, forming the tails stream. The difference in diffusion coefficientts between particles of the excited and unexcited isotopes is enhanced by the greater mass differences resulting from aggregation of unexcited particles into dimers and larger clusters. Prior art separation techniques which exploit differences in isotopic diffusion rates will consequently exhibit enhanced enrichment per stage by the utilization of the present invention

  15. Separation and Analysis of Boron Isotope in High Plant by Thermal Ionization Mass Spectrometry

    Directory of Open Access Journals (Sweden)

    Qingcai Xu

    2015-01-01

    Full Text Available Knowledge of boron and its isotope in plants is useful to better understand the transposition and translocation of boron within plant, the geochemical behavior in the interface between soil and plant, and the biogeochemical cycle of boron. It is critical to develop a useful method to separate boron from the plant for the geochemical application of boron and its isotope. A method was developed for the extraction of boron in plant sample, whose isotope was determined by thermal ionization mass spectrometry. The results indicated that this method of dry ashing coupled with two-step ion-exchange chromatography is powerful for the separation of boron in plant sample with large amounts of organic matters completely. The ratios of boron isotope composition in those plant tissue samples ranged from -19.45‰ to +28.13‰ (total range: 47.58‰ with a mean value of 2.61±11.76‰ SD. The stem and root isotopic compositions were lower than those in flower and leaf. The molecular mechanism of boron isotope may be responsible for the observed variation of boron isotopic composition and are considered as a useful tool for the better understanding of boron cycling process in the environment and for the signature of living systems.

  16. Experimental results to determine the separation performance of the packages used in cryogenic distillation isotopes

    International Nuclear Information System (INIS)

    Bornea, A.M.; Stefanescu, I.; Zamfirache, M.; Balteanu, O.; Preda, A.

    2007-01-01

    The cryogenic distillation of the hydrogen isotopes represents the back-end separation process most efficient and usually used in detritiation technologies. In our institute there were made many researches in the field of hydrogen isotopes separation. The first results were obtained based on an experimental installation - Pilot Plant for heavy water production - and in present days using a Detritiation Pilot Plant. In our Institute, was manufactured and patented a lot of hydrophilic package for isotopic distillation of water and hydrogen and also catalysts used for isotopic exchange waterhydrogen. This items was continuously developed in order to increase the isotopic separation efficiency. The goal of this paper is to determine by experimental work the performance of the package manufactured in our institute used in the cryogenic distillation process. To describe the separation performances was developed a mathematical model for the cryogenic distillation of the hydrogen isotopes. In order to determine the characteristics of the package, the installation was operated in the total reflux mode, for different flow rate for the liquid. There were made several experiments considering different operating conditions corresponding to various values for the refrigeration power in the column condenser. From the bottom and the top of the distillation column there were extracted samples in order to determine the isotopic composition. Processing the experimental data obtained from these tests using the Fenske relation, we obtained the separation efficiency function of the power inside the column boiler, operating pressure and also pressure drop along the package. This efficiency is describe by the number of theoretical plates per meter (NTT/m) or by equivalent height of one theoretical plate (IETT). (orig.)

  17. Experimental results to determine the separation performance of the packages used in cryogenic distillation isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Bornea, A.M.; Stefanescu, I.; Zamfirache, M.; Balteanu, O.; Preda, A.

    2007-07-01

    The cryogenic distillation of the hydrogen isotopes represents the back-end separation process most efficient and usually used in detritiation technologies. In our institute there were made many researches in the field of hydrogen isotopes separation. The first results were obtained based on an experimental installation - Pilot Plant for heavy water production - and in present days using a Detritiation Pilot Plant. In our Institute, was manufactured and patented a lot of hydrophilic package for isotopic distillation of water and hydrogen and also catalysts used for isotopic exchange waterhydrogen. This items was continuously developed in order to increase the isotopic separation efficiency. The goal of this paper is to determine by experimental work the performance of the package manufactured in our institute used in the cryogenic distillation process. To describe the separation performances was developed a mathematical model for the cryogenic distillation of the hydrogen isotopes. In order to determine the characteristics of the package, the installation was operated in the total reflux mode, for different flow rate for the liquid. There were made several experiments considering different operating conditions corresponding to various values for the refrigeration power in the column condenser. From the bottom and the top of the distillation column there were extracted samples in order to determine the isotopic composition. Processing the experimental data obtained from these tests using the Fenske relation, we obtained the separation efficiency function of the power inside the column boiler, operating pressure and also pressure drop along the package. This efficiency is describe by the number of theoretical plates per meter (NTT/m) or by equivalent height of one theoretical plate (IETT). (orig.)

  18. First measurements on the core and edge isotope composition using the JET isotope separator neutral particle analyser

    International Nuclear Information System (INIS)

    Bettella, D; Murari, A; Stamp, M; Testa, D

    2003-01-01

    Direct measurements of tokamak plasmas isotope composition are in general quite difficult and have therefore been very seldom performed. On the other hand, the importance of this measurement is going to increase, as future experiments will be progressively focused on plasmas approaching reactor conditions. In this paper, we report for the first time encouraging experimental evidence supporting a new method to determine the radial profile of the density ratio n H /(n H + n D ), based on neutral particle analyser (NPA) measurements. The measurements have been performed in JET with the ISotope SEParator (ISEP), a NPA device specifically developed to measure the energy spectra of the three hydrogen isotopes with very high accuracy and low cross-talk. The data presented here have been collected in two different experimental conditions. In the first case, the density ratio has been kept constant during the discharge. The isotope ratio derived from the ISEP has been compared with the results of visible spectroscopy at the edge and with the isotope composition derived from an Alfven eigenmodes active diagnostic (AEAD) system at about half the minor radius for the discharges reported in this paper. A preliminary evaluation of the additional heating effects on the measurements has also been carried out. In the second set of experiments, the isotope composition of deuterium plasmas has been abruptly changed with suitable short blips of hydrogen, in order to assess the capability of the method to study the transport of the hydrogen isotope species. Future developments of the methodology and its applications to the evaluation of hydrogen transport coefficients are also briefly discussed. The results obtained so far motivate further development of the technique, which constitutes one of the few candidate diagnostic approaches viable for ITER

  19. Doppler and time-travel broadening in ICR plasma isotope separation

    International Nuclear Information System (INIS)

    Karchevskii, A.I.; Potanin, E.P.

    1994-01-01

    Isotopically-selective ion-cyclotron resonance (ICR) heating is one of the most promising plasma isotope separation methods. The separation degree of ICR separation in a plasma depends on the resonance heating selectivity. The selectivity is due to the isotopically-adjacent accelerated ions resonance curve overlapping and therefore, is determined by the width of the resonance curves. In the case of a collisionless plasma in an ideal homogeneous longitudinal magnetic field, the line broadening is mainly determined by Doppler and time-travel effects. These effects differ in nature, and one has some difficulties in distinguishing them when interpreting the resonance curves because both broadenings depend on ion axial velocities. We consider the simplest case: the extrenal heating alternating electric field does not depend on the axial coordinate (the wave number γ = 0). Hence, in this case the Doppler effect does not occur

  20. Studies on separation of lithium isotopes by solvent extraction: Pt. 2

    International Nuclear Information System (INIS)

    Chen Yaohuan; Yan Jinying; Li Yongkun

    1987-01-01

    The effect of the struture of chelating agent and synergetic agent on the extraction separation of lithium isotopes by Sudan I-neutral ligand synergetic extraction systems were discussed in this paper. In order to obtain higher isotopic effect, the chelating agent must possess weaker acidity (pK a > 11), stronger intramolecular hydrogen bonding and a greater tendency to form a six-membered chelating ring. In the synergetic agent, there must be a functional group possessing strong coordination ability without steric hindrance. The separation effect (α) increased with the increase in the basicity of the coordinating group. The increase of the number of chelating rings in the extractable complex was of benefit to the enhancement of α. Further discussions are also made on the enrichment direction of extraction systems and the prospects of different systems to be used for isotope separation

  1. Lithium isotopic separation: preliminary studies; Separacao isotopica de litio: estudos preliminares

    Energy Technology Data Exchange (ETDEWEB)

    Macedo, Sandra Helena Goulart de

    1998-07-01

    In order to get the separation of natural isotopes of lithium by electrolytic amalgamation, an electrolytic cell with a confined mercury cathode was used to obtain data for the design of a separation stage. The initial work was followed by the design of a moving mercury cathode electrolytic cell and three experiments with six batches stages were performed for the determination of the elementary separation factor. The value obtained, 1.053, was ill agreement: with the specialized literature. It was verified in all experiments that the lithium - 6 isotope concentrated in the amalgam phase and that the lithium - 7 isotope concentrated in the aqueous phase. A stainless-steel cathode for the decomposition of the lithium amalgam and the selective desamalgamation were also studied. In view of the results obtained, a five stages continuous scheme was proposed. (author)

  2. Separative analyses of a chromatographic column packed with a core-shell adsorbent for lithium isotope separation

    International Nuclear Information System (INIS)

    Sugiyama, T.; Sugura, K.; Enokida, Y.; Yamamoto, I.

    2015-01-01

    Lithium-6 is used as a blanket material for sufficient tritium production in DT fueled fusion reactors. A core-shell type adsorbent was proposed for lithium isotope separation by chromatography. The mass transfer model in a chromatographic column consisted of 4 steps, such as convection and dispersion in the column, transfer through liquid films, intra-particle diffusion and and adsorption or desorption at the local adsorption sites. A model was developed and concentration profiles and time variation in the column were numerically simulated. It became clear that core-shell type adsorbents with thin porous shell were saturated rapidly relatively to fully porous one and established a sharp edge of adsorption band. This is very important feature because lithium isotope separation requires long-distance development of adsorption band. The values of HETP (Height Equivalent of a Theoretical Plate) for core-shell adsorbent packed column were estimated by statistical moments of the step response curve. The value of HETP decreased with the thickness of the porous shell. A core-shell type adsorbent is, then, useful for lithium isotope separation. (authors)

  3. Industrial scale production of stable isotopes employing the technique of plasma separation

    International Nuclear Information System (INIS)

    Stevenson, N.R.; Bigelow, T.S.; Tarallo, F.J.

    2003-01-01

    Calutrons, centrifuges, diffusion and distillation processes are some of the devices and techniques that have been employed to produce substantial quantities of enriched stable isotopes. Nevertheless, the availability of enriched isotopes in sufficient quantities for industrial applications remains very restricted. Industries such as those involved with medicine, semiconductors, nuclear fuel, propulsion, and national defense have identified the potential need for various enriched isotopes in large quantities. Economically producing most enriched (non-gaseous) isotopes in sufficient quantities has so far eluded commercial producers. The plasma separation process is a commercial technique now available for producing large quantities of a wide range of enriched isotopes. Until recently, this technique has mainly been explored with small-scale ('proof-of-principle') devices that have been built and operated at research institutes. The new Theragenics TM facility at Oak Ridge, TN houses the only existing commercial scale PSP system. This device, which successfully operated in the 1980's, has recently been re-commissioned and is planned to be used to produce a variety of isotopes. Progress and the capabilities of this device and it's potential for impacting the world's supply of stable isotopes in the future is summarized. This technique now holds promise of being able to open the door to allowing new and exciting applications of these isotopes in the future. (author)

  4. Modelling carbon membranes for gas and isotope separation.

    Science.gov (United States)

    Jiao, Yan; Du, Aijun; Hankel, Marlies; Smith, Sean C

    2013-04-14

    Molecular modelling has become a useful and widely applied tool to investigate separation and diffusion behavior of gas molecules through nano-porous low dimensional carbon materials, including quasi-1D carbon nanotubes and 2D graphene-like carbon allotropes. These simulations provide detailed, molecular level information about the carbon framework structure as well as dynamics and mechanistic insights, i.e. size sieving, quantum sieving, and chemical affinity sieving. In this perspective, we revisit recent advances in this field and summarize separation mechanisms for multicomponent systems from kinetic and equilibrium molecular simulations, elucidating also anomalous diffusion effects induced by the confining pore structure and outlining perspectives for future directions in this field.

  5. Separation of hydrogen isotope by hydrogen-water exchange

    International Nuclear Information System (INIS)

    Isomura, Shohei; Kaetsu, Hayato; Nakane, Ryohei

    1979-01-01

    The deuterium exchange reaction between gaseous hydrogen and liquid water is studied by use of three kinds of trickle bed exchange columns packed with hydrophobic catalysts supporting platinum. All columns have the effective lengths of 30 cm. They are 17 mm, 30 mm, and 95 mm in diameters, respectively. The separation experiments are carried out by the once-through methods. The separation efficiencies of the columns are evaluated by the parameters such as the height equivalent to a theoretical plate (H. E. T. P.) and the mass transfer co-efficient. It is found that the operating condition of the exchange column is optimum when the superficial hydrogen flow velocity is 0.3 m/sec. (author)

  6. Uranium isotopic separation by aerodynamic methods. Final report

    International Nuclear Information System (INIS)

    Davidovitz, P.; Anderson, J.B.; Brook, J.W.; Calia, V.S.; Greene, G.T.

    1979-06-01

    Two aerodynamic separation techniques for uranium enrichment were investigated for technical feasibility and economic viability. These techniques are known as the Jet Membrane and Velocity Slip Processes. Both analytical and laboratory studies were conducted to explore the technical feasibility of the subject processes. The Jet Membrane Process Studies demonstrated that the process was feasible and that a condensable gas carrier is available. The Velocity Slip Studies demonstrated the predicted effects and did not identify a suitable condensable gas carrier. Hence the Velocity Slip Process exhibited a larger power consumption than did the Jet Membrane Process. An independent contractor prepared detailed cost estimates of the process. The independent results indicated that, based on the same costing ground rules, the Velocity Slip process would require 16 times the fixed capital costs and 12 times the cost per separative work unit as compared to the Jet Membrane Process. The same cost structure indicated that the cost per separative work unit for the Jet Membrane process would be two to three times that for the Gas Centrifuge process. There are a number of uncertainties associated with these cost estimates, such that, in the extreme, the costs might be the same. Further, more detailed cost analysis would be required to resolve the uncertainties associated with the initial cost estimates. The conduct of new studies was not considered to be appropriate for EPRI because of the changes in enrichment program management and security philosophy discussed in the text

  7. Garden hose separation of gaseous isotopes. Part II. Supersonic accelerations

    International Nuclear Information System (INIS)

    Wang, C.G.; Davis, A.G.M.

    1979-01-01

    A mechanical process for separating gaseous mixtures according to their respective molecular weights, by a variation of the time-of-flight process, is proposed. The separative apparatus consists of several sets of nozzle-deflector combinations surrounded by a stationary collector housed in an evacuated chamber. From a rotating supersonic nozzle, a contiguous plurality of successive groups of molecules is ejected to form a continuous stream of the mixture. The molecules of each group of molecules are allowed to accelerate for a predetermined period of time following their supersonic expansion, thereby allowing each group of molecules to form a generally spherical configuration, the outer radius of which will be enriched in molecules of lighter mass, relative to lesser radii. A deflector means co-rotating with the nozzle is used to deflect molecules that have been allowed to move for the predetermined period of time in accordance with their expansion velocities, from at least one desired portion of the stream, and a stationary collector means is disposed to receive the deflected molecules. The estimated separative work produced from such a unit is about the same or better than that of a modern giant diffuser of similar dimensions. However, with an essentially empty chamber, the unit capital cost as well as the energy required is competitive with any of the well-known methods, mechanical or otherwise

  8. Multi-purpose hydrogen isotopes separation plant design

    Energy Technology Data Exchange (ETDEWEB)

    Boniface, H.A.; Gnanapragasam, N.V.; Ryland, D.K.; Suppiah, S.; Castillo, I. [Atomic Energy of Canada Limited - AECL, Chalk River, ON (Canada)

    2015-03-15

    There is a potential interest at AECL's Chalk River Laboratories to remove tritium from moderately tritiated light water and to reclaim tritiated, downgraded heavy water. With only a few limitations, a single CECE (Combined Electrolysis and Catalytic Exchange) process configuration can be designed to remove tritium from heavy water or light water and upgrade heavy water. Such a design would have some restrictions on the nature of the feed-stock and tritium product, but could produce essentially tritium-free light or heavy water that is chemically pure. The extracted tritium is produced as a small quantity of tritiated heavy water. The overall plant capacity is fixed by the total amount of electrolysis and volume of catalyst. In this proposal, with 60 kA of electrolysis a throughput of 15 kg*h{sup -1} light water for detritiation, about 4 kg*h{sup -1} of heavy water for detritiation and about 27 kg*h{sup -1} of 98% heavy water for upgrading can be processed. Such a plant requires about 1,000 liters of AECL isotope exchange catalyst. The general design features and details of this multi-purpose CECE process are described in this paper, based on some practical choices of design criteria. In addition, we outline the small differences that must be accommodated and some compromises that must be made to make the plant capable of such flexible operation. (authors)

  9. A new type separation column for the water-hydrogen isotope catalytic exchange process

    International Nuclear Information System (INIS)

    Fedorchenko, O.A.; Alekseev, I.A.; Trenin, V.D.

    2001-01-01

    The catalytic water/hydrogen isotope exchange process is by right considered the most attractive for the solution a number of urgent problems of hydrogen isotope separation. A new type exchange reaction column is described and studied in details by computer simulation and with the help of McCabe-Thiele diagrams. It is shown that the new column in comparison with a traditional one needs less catalyst quantity and a smaller diameter for the solving of the same separation tasks. Generalized calculation data are presented in graphical form

  10. Connection experiments with a hollow cathode ion source and a helium gas jet system for on-line isotope separation

    International Nuclear Information System (INIS)

    Mazumdar, A.K.; Wagner, H.; Walcher, W.; Lund, T.

    1976-01-01

    A helium jet system was connected to a hollow cathode ion source. Using fission products the efficiencies of the different steps were measured by β-, X-ray and γ-counting while the mass spectrum and the focussing of the extracted ion beam were observed with a small deflecting magnet. Mean transport efficiencies of 50% through the 12 m capillary were obtained and ion source efficiencies in the percent range for several elements. (Auth.)

  11. Separation of boron isotopes by ion exchange chromatography: studies with Duolite-162, a type-II resin

    International Nuclear Information System (INIS)

    Sharma, B.K.; Subramanian, R.; Balasubramanian, R.; Mathur, P.K.

    1994-01-01

    The selection of resin plays an important role in the process of separation of boron isotopes by ion exchange chromatography. The determination of (i) ion exchange capacity of Duolite-162 resin for hydroxyl - chloride exchange, (ii) hydroxyl - borate exchange, (iii) isotopic exchange separation factor by batch method and (iv) effect of concentration of boric acid on isotopic exchange separation factor to test the suitability of the above resin for this process are discussed in this report. (author)

  12. On-line SPE-UHPLC method using fused core columns for extraction and separation of nine illegal dyes in chilli-containing spices.

    Science.gov (United States)

    Khalikova, Maria A; Satínský, Dalibor; Smidrkalová, Tereza; Solich, Petr

    2014-12-01

    The presented work describes the development of a simple, fast and effective on-line SPE-UHPLC-UV/vis method using fused core particle columns for extraction, separation and quantitative analysis of the nine illegal dyes, most frequently found in chilli-containing spices. The red dyes Sudan I-IV, Sudan Red 7B, Sudan Red G, Sudan Orange G, Para Red, and Methyl Red were separated and analyzed in less than 9 min without labor-consuming pretreatment procedure. The chromatographic separation was performed on Ascentis Express RP-Amide column with gradient elution using mixture of acetonitrile and water, as a mobile phase at a flow rate of 1.0 mL min(-1) and 55°C of temperature. As SPE sorbent for cleanup and pre-concentration of illegal dyes short guard fused core column Ascentis Express F5 was used. The applicability of proposed method was proven for three different chilli-containing commercial samples. Recoveries for all compounds were between 90% and 108% and relative standard deviation ranged from 1% to 4% for within- and from 2% to 6% for between-day. Limits of detection showed lower values than required by European Union regulations and were in the range of 3.3-10.3 µg L(-1) for standard solutions, 5.6-235.6 µg kg(-1) for chilli-containing spices. Copyright © 2014 Elsevier B.V. All rights reserved.

  13. Mass and heat transfer on B7 ordered packing in hydrogen isotope separation by distillation

    International Nuclear Information System (INIS)

    Croitoru, Cornelia; Pop, Floarea; Titescu, Gheorghe; Stefanescu, Ioan; Trancota, Dan; Peculea, Marius

    2002-01-01

    This work presents theoretical and experimental data referring to mass and heat transfer on B7 ordered packing in deuterium isotope separation by distillation. The first part is devoted to the study of mass transfer in hydrogen isotopic distillation while the second one treats the mass and heat transfer in water isotopic distillation. A stationary mathematical model for the mass and heat transfer was developed based on multitubular column model with wet wall. This model allowed the calculation starting from theoretical data of the ordered packing efficiency, expressed by the transfer unit height, TUH. Also, from theoretical data the mass and heat transfer coefficients were determined. A test of the mathematical model was performed with the experimental data obtained from two laboratory installations for hydrogen isotope separation by distillation. From the first installation, experimental data concerning the B7 ordered packing efficiency were obtained for the deuterium separation by cryogenic distillation at the - 250 deg C level. With the second one data referring to the mass and heat transfer on the same packing were obtained for the deuterium separation by water distillation under vacuum at the 60 deg C level. The values of TUH, mass and heat transfer coefficients as theoretically evaluate and experimentally checked are in agreement with the respective values obtained in separation processes in chemical industry. This is the fact which endorses utilization of the model of multitubular column with wet wall for describing the transfer processes in distillation columns equipped with B7 ordered packing

  14. Investigation related to hydrogen isotopes separation by cryogenic distillation

    International Nuclear Information System (INIS)

    Bornea, A.; Zamfirache, M.; Stefanescu, I.; Preda, A.; Balteanu, O.; Stefan, I.

    2008-01-01

    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)

  15. Studies on cryogenic distillation columns for hydrogen isotope separation

    International Nuclear Information System (INIS)

    Kinoshita, Masahiro

    1984-08-01

    Cryogenic distillation is applicable to a number of situations. The feed condition, column cascade configuration, input and output specifications vary greatly from situation to situation. In the mainstream fuel circulation system for a fusion reactor, the feed composition may fluctuate greatly during the operation. The radiological standards for tritium lost to the environment are increasingly becoming stricter. Systematic studies are needed to achieve the goal of long-term operation meeting the strict requirements for products even under great fluctuation of the feed condition in all the situations. The present report gives a critical, brief review of the studies which have been made by the author. The subjects treated are development of computer simulation procedures, analysis on an H-T separation column with a feedback stream, dynamics and control, proposal of a new cascade, analysis on helium effects on column behavior, start-up analysis for a cascade, and preliminary experimental study on dependence of HETP on operational conditions. (author)

  16. Present and prospective situation in laser isotope separation: will the free electron laser be needed

    International Nuclear Information System (INIS)

    Rigny, P.

    1984-09-01

    The need for enriched isotopes, as it appears to day will be recalled for the foreseeable future, this need, in quantitative terms, will be confined to isotopes for nuclear energy. The interest of laser isotope separation will finally depend on our ability to fulfil a number of requirements as to the laser output light characteristics. These will be recalled for the most common laser processes (molecular photodissociation and atomic photoionisation). At this point a comparison with expectations from the FEL can already be attempted. Less common laser isotope separation schemes can gain interest from the possibilities opened by the FEL, especially by access to new wavelengths ranges. Some schemes implying UV or VUV photons will be discussed, as well as some possibilities involving IR photons. Attention will be paid to the problems that arise when considering scaled-up isotope separation installations. A large scale process results in more constraints on the laser parameters. Estimation of FEL capacity in this respect will be attempted

  17. Experimental determination of one- and two-neutron separation energies for neutron-rich copper isotopes

    Science.gov (United States)

    Yu, Mian; Wei, Hui-Ling; Song, Yi-Dan; Ma, Chun-Wang

    2017-09-01

    A method is proposed to determine the one-neutron S n or two-neutron S 2n separation energy of neutron-rich isotopes. Relationships between S n (S 2n) and isotopic cross sections have been deduced from an empirical formula, i.e., the cross section of an isotope exponentially depends on the average binding energy per nucleon B/A. The proposed relationships have been verified using the neutron-rich copper isotopes measured in the 64A MeV 86Kr + 9Be reaction. S n, S 2n, and B/A for the very neutron-rich 77,78,79Cu isotopes are determined from the proposed correlations. It is also proposed that the correlations between S n, S 2n and isotopic cross sections can be used to find the location of neutron drip line isotopes. Supported by Program for Science and Technology Innovation Talents at Universities of Henan Province (13HASTIT046), Natural and Science Foundation in Henan Province (162300410179), Program for the Excellent Youth at Henan Normal University (154100510007) and Y-D Song thanks the support from the Creative Experimental Project of National Undergraduate Students (CEPNU 201510476017)

  18. Cost analysis of lasers for a laser isotope separation system. Final report

    International Nuclear Information System (INIS)

    Mail, R.A.; Markovich, F.J.; Carr, R.H.

    1977-01-01

    To be of practical significance, laser isotope separation (LIS) for separation of 235 U from 238 U must exhibit attributes which make it preferable to expansion of the present facilities. Clearly the most attractive such attribute is the prospect of significant cost reductions, which preliminary studies at LLL suggest will amount to a factor of three and perhaps as much as ten. From these preliminary studies, it appears that the lasers themselves account for a very substantial portion of the capital cost of a LIS system, and a significant portion of the equipment replacement costs. Since the laser costs are so pivotal to the system cost, and the system cost is so pivotal to the choice of separation techniques, it is clear that a more detailed investigation of laser costs is required. Results are presented of a study performed by General Research Corporation (GRC) to assess the cost of lasers in a production laser isotope separation (LIS) plant

  19. Modified molecular sieves: stationary phase for the gas chromatographic separation of hydrogen isotopes

    International Nuclear Information System (INIS)

    Pushpa, K.K.; Annaji Rao, K.; Iyer, R.M.

    1993-01-01

    Gas chromatographic separation of hydrogen isotopes on different molecular sieves at liquid nitrogen temperature has been investigated. Normal molecular sieves 5A, 13X and AW500 are not satisfactory for the purpose both in the partially dehydrated as well as totally dehydrated state. Molecular sieve 4A in partially dehydrated state separated H 2 and D 2 while H 2 and HD are not well resolved. Iron exchanged or coated molecular sieves 4A, 5A, 13X and AW500 in the partially dehydrated state separated the isotopic mixtures H 2 , HD, D 2 and H 2 , HT, T 2 . The resolution varied depending on the amount of iron content and the residual moisture in the molecular sieves. Good separations were obtained on 15% Fe coated molecular sieve 5A and 5% Fe coated molecular sieve 4A. (author). 18 refs., 6 figs., 3 tabs

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2011-03-01

    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

  1. Stable Isotope Quantitative N-Glycan Analysis by Liquid Separation Techniques and Mass Spectrometry.

    Science.gov (United States)

    Mittermayr, Stefan; Albrecht, Simone; Váradi, Csaba; Millán-Martín, Silvia; Bones, Jonathan

    2017-01-01

    Liquid phase separation analysis and subsequent quantitation remains a challenging task for protein-derived oligosaccharides due to their inherent structural complexity and diversity. Incomplete resolution or co-detection of multiple glycan species complicates peak area-based quantitation and associated statistical analysis when optical detection methods are used. The approach outlined herein describes the utilization of stable isotope variants of commonly used fluorescent tags that allow for mass-based glycan identification and relative quantitation following separation by liquid chromatography (LC) or capillary electrophoresis (CE). Comparability assessment of glycoprotein-derived oligosaccharides is performed by derivatization with commercially available isotope variants of 2-aminobenzoic acid or aniline and analysis by LC- and CE-mass spectrometry. Quantitative information is attained from the extracted ion chromatogram/electropherogram ratios generated from the light and heavy isotope clusters.

  2. Two-Dimensional Capillary Electrophoresis with On-Line Sample Preparation and Cyclodextrin Separation Environment for Direct Determination of Serotonin in Human Urine.

    Science.gov (United States)

    Piešťanský, Juraj; Maráková, Katarína; Mikuš, Peter

    2017-10-07

    An advanced two-dimensional capillary electrophoresis method, based on on-line combination of capillary isotachophoresis and capillary zone electrophoresis with cyclodextrin additive in background electrolyte, was developed for effective determination of serotonin in human urine. Hydrodynamically closed separation system and large bore capillaries (300-800 µm) were chosen for the possibility to enhance the sample load capacity, and, by that, to decrease limit of detection. Isotachophoresis served for the sample preseparation, defined elimination of sample matrix constituents (sample clean up), and preconcentration of the analyte. Cyclodextrin separation environment enhanced separation selectivity of capillary zone electrophoresis. In this way, serotonin could be successfully separated from the rest of the sample matrix constituents migrating in capillary zone electrophoresis step so that human urine could be directly (i.e., without any external sample preparation) injected into the analyzer. The proposed method was successfully validated, showing favorable parameters of sensitivity (limit of detection for serotonin was 2.32 ng·mL -1 ), linearity (regression coefficient higher than 0.99), precision (repeatability of the migration time and peak area were in the range of 0.02-1.17% and 5.25-7.88%, respectively), and recovery (ranging in the interval of 90.0-93.6%). The developed method was applied for the assay of the human urine samples obtained from healthy volunteers. The determined concentrations of serotonin in such samples were in the range of 12.4-491.2 ng·mL -1 that was in good agreement with literature data. This advanced method represents a highly effective, reliable, and low-cost alternative for the routine determination of serotonin as a biomarker in human urine.

  3. Effect of nonequilibrium degree on separation factor in carbon isotope separation by CO2 microwave discharge

    International Nuclear Information System (INIS)

    Masaaki Suzuki; Shinsuke Mori; Noritaka Matsumoto; Hiroshi Akatsuka

    1999-01-01

    The local separation factor and the local nonequilibrium degree just behind the plasma region were obtained. The plasma gas compositions measured by the enthalpy probe system were substantially thermodynamic nonequilibrium conditions, when the input energy was 4 J/cm 3 . The measured maximum value of the separation factor was 1.01, although it changed locally. The measured separation factor and its nonequilibrium condition were discussed. Anyway, the only small value obtained in this experiments is similar to the recent data obtained by Kurchatov group and is less than published data, which is measured spectroscopically [ru

  4. Method of separation of fission and corrosion products and of corresponding isotopes from liquid waste

    International Nuclear Information System (INIS)

    Prochazka, H.; Stamberg, K.; Jilek, R.; Hulak, P.; Katzer, J.

    1976-01-01

    A method of separating fission and corrosion products and corresponding stable isotopes from liquid waste is described. Mycelia of fungi are used as sorbents for retaining these products on their surface and within their pores. Methods of activation or regeneration of the sorbent are outlined. 11 claims

  5. Observation of new levels for isotope separation in atomic uranium by multistep ionization

    International Nuclear Information System (INIS)

    Carlson, L.R.; Solarz, R.W.; Paisne, J.A.; Worden, E.F.; May, C.A.; Johnson, S.A.

    1975-01-01

    Over 100 new odd parity levels useful for isotope separation of U(I) were observed between 32,660--34,165 cm -1 using multistep photoionization. A tabulation of typical cross sections and radiative lifetimes for these states is given. The extension of this technique to mapping the spectra of other heavy atoms is discussed

  6. Separation of 15N by isotopic exchange in NO, NO2-HNO3 system under pressure

    International Nuclear Information System (INIS)

    Axente, D.; Baldea, A.; Teaca, C.; Horga, R.; Abrudean, M.

    1998-01-01

    One of the most used method for production of 15 N with 99% at. concentration is the isotopic exchange between gaseous nitrogen oxides and HNO 3 solution 10M: ( 15 NO, 15 NO 2 ) g + H 14 NO 3,l = ( 14 NO, 14 NO 2 ) g + H 15 NO 3,l . The isotopic exchange is characterized by an elemental separation factor α=1.055 at 25 deg. C and atmospheric pressure. Recently, kinetics data pointed to the linear dependence of the exchange rate 15 N/ 14 N(R) on the nitrogen oxide pressure with a rate law R = k[HNO 3 ] 2 · [N 2 O 3 ]. In this work, the influence of the nitrogen oxide pressure on the 15 N separation efficiency was determined by the use of a laboratory equipment with a separation column pack of Helipack type, with dimensions 1.8 mm x 1.8 mm x 0.2 mm. The increase of nitrogen oxide pressure led to a better isotopic transfer between the two counter-flow phases in the column pack. The HETP (Height Equivalent to a Theoretical Plate) determined for a 3.14 ml ·cm -2 · min -1 load is equal to that obtained at atmospheric pressure for a two times lower load. The operation of the equipment for isotopic separation of 15 N at 1.8 atm instead of atmospheric pressure allows doubling the HNO 3 10 M load of the column and consequently, doubling the production rate. A better performance of the separation process at higher pressure is essential for the industrial production of 15 N isotope which is used for the production of uranium nitride in FBR type reactors. (authors)

  7. Oxygen isotope separation by isotopically selective infrared multiphoton dissociation of 2,3-dihydropyran

    International Nuclear Information System (INIS)

    Yokoyama, Atsushi; Ohba, Hironori; Akagi, Hiroshi; Yokoyama, Keiichi; Saeki, Morihisa; Katsumata, Keiichi

    2008-01-01

    Oxygen isotopic selectivity on infrared multiphoton dissociation of 2,3-dihydropyran has been studied by the examination of the effects of excitation frequency, laser fluence, and gas pressure on the dissociation probability of 2,3-dihydropyran and isotopic composition of products. Oxygen-18 was enriched in a dissociation product: 2-propenal. The enrichment factor of 18 O and the dissociation probability were measured at laser frequency between 1033.5 and 1057.3 cm -1 ; the laser fluence of 2.2 - 2.3 J/cm 2 ; and the 2,3-dihydropyran pressure of 0.27 kPa. The dissociation probability decreases as the laser frequency being detuned from the absorption peak of 2,3-dihydropyran around 1081 cm -1 . On the other hand, the enrichment factor increases with detuning the frequency. The enrichment factor of 18 O increases with increasing the 2,3-dihydropyran pressure at the laser fluence below 3 J/cm 2 and the laser frequency of 1033.5 cm -1 , whereas the yield of 2-propenal decreases with increasing the pressure. Very high enrichment factor of 751 was obtained by the irradiation of 0.53 kPa of 2,3-dihydropyran at 2.1 J/cm 2 . (author)

  8. Characteristic analysis of laser isotope separation process by two-step photodissociation method

    International Nuclear Information System (INIS)

    Okamoto, Tsuyoshi; Suzuki, Atsuyuki; Kiyose, Ryohei

    1981-01-01

    A large number of laser isotope separation experiments have been performed actively in many countries. In this paper, the selective two-step photodissociation method is chosen and simultaneous nonlinear differential equations that express the separation process are solved directly by using computer. Predicted separation factors are investigated in relation to the incident pulse energy and the concentration of desired molecules. Furthermore, the concept of separative work is used to evaluate the results of separation for this method. It is shown from an example of numerical calculation that a very large separation factor can be obtained if the concentration of desired molecules is lowered and two laser pulses to be closely synchronized are not always required in operation for the photodissociation of molecules. (author)

  9. Isothermal and non-isothermal conditions of isotope separation by chemical exchange method

    International Nuclear Information System (INIS)

    Khoroshilov, A.V.; Andreev, B.M.; Katalnikov, S.G.

    1992-01-01

    The published data about the effect of temperature on thermodynamic and mass transfer parameters of isotope separation by the chemical exchange method were used to examine the influence of iso- and non-isothermal conditions on the effectiveness of the separation process. It has been shown that simultaneous fulfillment of several optimization criteria is impossible in optimization of the isothermal process. If the limitation that temperature must be constant in the whole range of concentrational changes for an isolated isotope is removed, then it is possible to solve the problem of optimization with simultaneous fulfillment of several optimization criteria. When the separation process is carried out with non-isothermal conditions, that is, in temperature cascade, then the maximum concentration change takes place at every theoretical separation plate, and whole cascade is characterised by maximum throughput, minimum height and volume, and minimum cost for the stream reflux. From the results of our study, it was concluded that in the optimum temperature cascade, the cost of production of unity quantity of isotope can be decreased at least by a factor of two as compared with the optimal isothermal version of the separation process. (author)

  10. Laser isotope separation by selective excited state photochemistry. Annual progress report, March 31, 1976--February 28, 1977

    International Nuclear Information System (INIS)

    Zare, R.N.

    1977-03-01

    Experimental results are presented providing insight into the mechanisms of photochemical separation of Cd isotopes by selective excitation of ICl in the presence of halogenated olefins. The types of scrambling reactions that can be expected in isotope separation by scavenging are discussed along with strategies for minimizing such reactions. The experimental results are summarized and the reaction mechanisms are represented by graphic equations

  11. Uranium isotope separation in the solid state. Progress report, December 1, 1976--June 1, 1977

    International Nuclear Information System (INIS)

    Bernstein, E.R.

    1977-06-01

    Since we were actively able to work on this project, we have been engaged in three separate lines of research. Each of these has been related to laser-induced isotope separation of uranium in the solid state. The three areas are: (a) improved reaction chemistry for both host materials Zr(BH 4 ) 4 and Hf(BH 4 ) 4 and U(BH 4 ) 4 itself; (b) improved spectroscopic techniques in order to obtain sharper spectra; and (c) solid state photochemical investigations to study U(BH 4 ) 4 photodecomposition mechanism and yield as a function of wave length. These are all integral parts of the solid state isotope separation procedure and are discussed in terms of the overall process proposed

  12. Validation of a simple isotopic technique for the measurement of global and separated renal function

    International Nuclear Information System (INIS)

    Chachati, A.; Meyers, A.; Rigo, P.; Godon, J.P.

    1986-01-01

    Schlegel and Gates described an isotopic method for the measurement of global and separated glomerular filtration rate (GFR) and effective renal plasma flow (ERPF) based on the determination by scintillation camera of the fraction of the injected dose (99mTc-DTPA-[ 131 I]hippuran) present in the kidneys 1-3 min after its administration. This method requires counting of the injected dose and attenuation correction, but no blood or urine sampling. We validated this technique by the simultaneous infusion of inulin and para-amino hippuric acid (PAH) in patients with various levels of renal function (anuric to normal). To better define individual renal function we studied 9 kidneys in patients either nephrectomized or with a nephrostomy enabling separated function measurement. A good correlation between inulin, PAH clearance, and isotopic GFR-ERPF measurement for both global and separate renal function was observed

  13. Rule of thumb for binary isotope separations in a gas centrifuge

    International Nuclear Information System (INIS)

    Berger, M.H.

    1985-12-01

    A very simple hypothetical model of the binary isotope separation process in a countercurrent Gas Centrifuge is proposed. Like the usual Cohen-Onsager separation theory it involves the internal fluid dynamics, but unlike the usual isotopic separation theory it completely obviates the usual flow integrals for Cohen's E. Thereby allowing an immediate estimate of the flow efficiency of a given design, which can and sometimes should be checked later by the usual analyses. To shed some light on our idea, two simple derivations for assumed idealized hydrodynamics are given, but a rigorous proof remains an open question. Then our hypothesis is tested against a battery of about 10 new ''exact'' formulas for E based upon analytical solutions to several variants of Onsager's pancake equation and found to be ''reasonably'' accurate and surprisingly robust. Finally, some limitations of our rule are explored

  14. Tritium isotope separation from light and heavy water by bipolar electrolysis

    International Nuclear Information System (INIS)

    Petek, M.; Ramey, D.W.; Taylor, R.D.; Kobisk, E.H.

    1980-01-01

    A process for separating tritium from light and heavy water is described. Hydrogen is transferred at and through bipolar electrodes at rates H > D > T. In a cell containing several bipolar electrodes placed in series between two terminal electrodes, a flow of hydrogen is established from the terminal anode compartment toward the terminal cathode. An electrolyte feed containing tritium is continuously added to the system and is subsequently transported countercurrent to the hydrogen mass transfer. A cascaded system is established, in which effluent streams enriched and depleted in tritium can be withdrawn. The voltage drop is smaller at any bipolar electrode as compared to the voltage for normal electrolysis. Cell design is compact because isotope separation occurs at bipolar electrodes without evolution of gas. Isotope separation was demonstrated in laboratory cells where a steady-state tritium concentration gradient was attained. This gradient was in agreement with concentrations calculated from a derived mathematical model

  15. Penning-trap Q-value determination of the 71Ga(ν,e−)71Ge reaction using threshold charge breeding of on-line produced isotopes

    International Nuclear Information System (INIS)

    Frekers, D.; Simon, M.C.; Andreoiu, C.; Bale, J.C.; Brodeur, M.; Brunner, T.; Chaudhuri, A.; Chowdhury, U.; Crespo López-Urrutia, J.R.; Delheij, P.; Ejiri, H.; Ettenauer, S.; Gallant, A.T.; Gavrin, V.; Grossheim, A.; Harakeh, M.N.; Jang, F.; Kwiatkowski, A.A.

    2013-01-01

    We present a first direct Q-value measurement of the 71 Ga(ν,e − ) 71 Ge reaction using the TITAN mass-measurement facility at ISAC/TRIUMF. The measurements were performed in a Penning trap on neon-like 71 Ga 21+ and 71 Ge 22+ using isobar separation of the on-line produced mother and daughter nuclei through threshold charge breeding in an electron-beam ion trap. In addition, isoionic samples of 71 Ga 21+ and 71 Ge 21+ were stored concurrently in the Penning trap and provided a separate Q-value measurement. Both independent measurements result in a combined Q-value of 233.5±1.2 keV, which is in agreement with the previously accepted Q-value for the ν cross-section calculations. Together with a recent measurement of the ν-response from the excited states in 71 Ge, we conclude that there are no further uncertainties in the nuclear structure, which could remove the persistent discrepancy between the SAGE and GALLEX calibration measurements performed with neutrinos from reactor-produced 51 Cr and 37 Ar sources and the theoretical expectation

  16. Electrical circuits of an electromagnetic isotope separator; Circuits electriques d'un separateur d'isotopes electromagnetique

    Energy Technology Data Exchange (ETDEWEB)

    Neyron, A. [Commissariat a l' energie atomique et aux energies alternatives - CEA, Centre d' etudes nucleaires de Saclay (France)

    1959-07-01

    After an outline of the general principles governing the operation of an electromagnetic isotope separator, the electrical characteristics necessary to this operation are given. First the electrical characteristics of the ion source are briefly presented. The author then gives a detailed account of the construction of the H.T. acceleration supply of which the maxima characteristics are 80 kV and 150 mA with stabilisation of the order of 4.10{sup -4}. Reprint of a paper published in 'Industries Atomiques' - n. 3-4, 1959.

  17. The 11th International ICIT Conference Progress in Cryogenics and Isotopes Separation. Proceedings

    International Nuclear Information System (INIS)

    Stefanescu, Ioan

    2005-01-01

    The proceedings of the 11th International ICIT Conference Progress in Cryogenics and Isotopes Separation held in Caciulata, Romania on 12-14 October 2005 contain plenary lectures (6 papers) and 6 sections addressing the following subject matters: Section 1. Stable Isotopes Physics. Technologies and Applications (5 papers); Section 2. Science and Materials Engineering (11 papers); Section 3. Nuclear Power (21 papers); Section 4. Hydrogen and Fuel Cells (7 papers); Section 5. Environmental Protection. Industrial Risk (10 papers); Section 6. Laboratory Analysis Methods (10 papers). Twenty two papers are available in abstract form only and full text entered the corresponding records

  18. The 12th International ICIT Conference Progress in Cryogenics and Isotopes Separation. Proceedings

    International Nuclear Information System (INIS)

    Stefanescu, Ioan

    2006-01-01

    The proceedings of the 12th International ICIT Conference Progress in Cryogenics and Isotopes Separation held in Caciulata, Romania on 25-27 October 2006 contain plenary lectures (11 papers) and 7 sections addressing the following subject matters: Section 1. Stable Isotopes Physics. Technologies and Applications (6 papers); Section 2. Cryogenics Technologies and Equipment (6 papers); Section 3. Science and Materials Engineering (18 papers); Section 4. Nuclear Power (17 papers); Section 5. Hydrogen and Fuel Cells (14 papers); Section 6. Environmental Protection. Industrial Risk (14 papers); Section 7. Laboratory Analysis Methods (13 papers). A number of 40 papers are available in abstract form only and accordingly full text entered the corresponding records

  19. Realization of an electromagnetic isotope separator. Application to the isotopes of the mass 93 from the molybdenum and the technetium

    International Nuclear Information System (INIS)

    Bernas, R.

    1954-07-01

    Analysis of focusing properties of a homogeneous magnetic field leads the author to use a magnetic sector of 60 deg, for the realization of an electromagnetic separator. The sources of realized ions provide ionic debits of 10 mA. The currents ionic detached isotopes to the collector vary from 1 to 5 mA. The separation efficiency is of 125 for a current collected of 1 mA. A survey of the neutralization of the space charge permitted to specify the role of the negative ions in this phenomenon. A method of neutralization of the space charge is proposed and gave excellent results. A report will be given of the separations of some elements: mercury, bromine, thorium, etc... The application of the separator to the study of the isomeric transfers in the molybdenum and the technetium permitted to assign definitely for 93 Mo and 93 Tc two radiances γ of respective energies 260 and 390 keV. A new process of fast chemical separation Mo/Tc is described. (author) [fr

  20. Progress in 15N and 13C separation by isotopic exchange

    International Nuclear Information System (INIS)

    Axente, D.

    2004-01-01

    An experimental study of 15 N separation by isotopic exchange in NO, NO 2 - HNO 3 system under pressure is presented. The pressure increase in 15 N separation plant improved the isotopic transport between the two phases circulated in counter-current in the packed column according to a better kinetics of isotopic exchange at higher pressures. The operation of 15 N separation plant at a pressure of 1.8 atm (absolute) will permit doubling of 10 M nitric acid flow rate and of 15 N production of a given column. The improved performance at a higher pressure is significant for large scale 15 N production, which would be utilized for uranium nitride fuels for FBRs. Enrichment of 13 C by chemical exchange between CO 2 and amine carbamate in nonaqueous solvent has been modelled. For process optimization the steady state separation and the height equivalent to a theoretical plate (HETP) have been determined for different experimental conditions and simulated for higher pressures than atmospheric one. At lower temperature (5 deg C) as the pressure increases the quantity of CO 2 dissolved in amine solution increases. For process analysis at higher pressures and lower temperatures, the two steps model has been considered. At 0.9 MPa pressure and 5 deg C the reaction rate is higher than at 25 deg C and atmospheric pressure, the value of HETP being lower with more than 100% than at 25 deg C. (author)

  1. Process and system for isotope separation using the selective vibrational excitation of molecules

    International Nuclear Information System (INIS)

    Woodroffe, J.A.; Keck, J.C.

    1976-01-01

    This invention concerns the separation of isotopes by using the isotopically selective vibrational excitation and the vibration-translation reactions of the excited particles. UF 6 molecular mixed with a carrier gas, such as argon, are directed through a refrigerated chamber lighted by a laser radiation tuned to excite vibrationally the uranium hexafluoride molecules of a particular uranium isotope. The density of the carrier gas is preferably maintained above the density of the uranium hexafluoride to allow a greater collision probability of the vibrationally excited molecules with a carried molecule. In such a case, the vibrationally excited uranium hexafluoride will collide with a carrier gas molecule provoking the conversion of the excitation energy into a translation of the excited molecule, resulting in thermal energy or greater diffusibility than that of the other uranium hexafluoride molecules [fr

  2. First on-line applications of multi-reflection time-of-flight mass separator at ISOLTRAP and the mass measurement of $^{82}$Zn

    CERN Document Server

    Wolf, Robert

    This thesis describes the implementation and first on-line application of a multi-reflection time-of-flight (MR-ToF) mass analyzer for high-resolution mass separation at the ISOLTRAP mass spectrometer at ISOLDE/CERN. On the one hand, the major objective was to improve ISOLTRAPs mass-measurement capabilities with respect to the ratio of delivered contaminating ions to ions of interest. On the other hand, the time necessary to purify wanted from unwanted species should be reduced as much as possible to enable access to even more exotic nuclei. The device has been set up, optimized and tested at the University of Greifswald before its move to ISOLTRAP. The achieved performance comprises mass resolving powers of up to 200000 reached at observation times of 30ms and a contamination suppression of about four orders of magnitude by use of a Bradbury-Nielsen gate. With the characteristics, it outperforms clearly the so far state-of-the-art purification method of a gas-filled Penning trap. To improve the utilization o...

  3. Special isotope separation project, Idaho National Engineering Laboratory, Idaho Falls, Idaho

    International Nuclear Information System (INIS)

    1988-02-01

    Construction and operation of a Special Isotope Separation (SIS) project using the Atomic Vapor Laser Isotope Separation (AVLIS) process technology at the Idaho National Engineering Laboratory (INEL) near Idaho Falls, Idaho are proposed. The SIS project would process fuel-grade plutonium administered by the Department of Energy (DOE) into weapon-grade plutonium using AVLIS and supporting chemical processes. The SIS project would require construction and operation of a Laser Support Facility to house the laser system and a Plutonium Processing Facility. The SIS project would be integrated with existing support and waste management facilities at the selected site. The SIS project would provide DOE with the capability of segregating the isotopes of DOE-owned plutonium into specific isotopic concentrations. This capability would provide redundancy in production capacity, technological diversity, and flexibility in DOE's production of nuclear materials for national defense. Use of the INEL site would impact 151,350 square meters (37.4 acres) of land, of which more than 70% has been previously disturbed. During construction, plant and animal habitat associated with a sagebrush vegetation community would be lost. During operation of the SIS facilities, unavoidable radiation exposures would include occupational exposures and exposures to the public from normal atmospheric releases of radioactive materials that would be minimal compared to natural background radiation

  4. Separation of polybrominated diphenyl ethers in fish for compound-specific stable carbon isotope analysis

    Energy Technology Data Exchange (ETDEWEB)

    Zeng, Yan-Hong [State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640 (China); Graduate University of Chinese Academy of Sciences, Beijing, 100049 (China); Luo, Xiao-Jun, E-mail: luoxiaoj@gig.ac.cn [State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640 (China); Chen, Hua-Shan; Wu, Jiang-Ping; Chen, She-Jun; Mai, Bi-Xian [State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640 (China)

    2012-05-15

    A separation and isotopic analysis method was developed to accurately measure the stable carbon isotope ratios of polybrominated diphenyl ethers (PBDEs) with three to six substituted bromine atoms in fish samples. Sample extracts were treated with concentrated sulfuric acid to remove lipids, purified using complex silica gel column chromatography, and finally processed using alumina/silica (Al/Si) gel column chromatography. The purities of extracts were verified by gas chromatography and mass spectrometry (GC-MS) in the full-scan mode. The average recoveries of all compounds across the purification method were between 60% and 110%, with the exception of BDE-154. The stable carbon isotopic compositions of PBDEs can be measured with a standard deviation of less than 0.5 Per-Mille-Sign . No significant isotopic fraction was found during the purification of the main PBDE congeners. A significant change in the stable carbon isotope ratio of BDE-47 was observed in fish carcasses compared to the original isotopic signatures, implying that PBDE stable carbon isotopic compositions can be used to trace the biotransformation of PBDEs in biota. - Highlights: Black-Right-Pointing-Pointer A method for the purification of PBDEs for CSIA was developed. Black-Right-Pointing-Pointer The {delta}{sup 13}C of PBDE congeners can be measured with a standard deviation of less than 0.5 Per-Mille-Sign . Black-Right-Pointing-Pointer Common carp were exposed to a PBDE mixture to investigate debromination. Black-Right-Pointing-Pointer Ratios of the {delta}{sup 13}C values can be used to trace the debromination of PBDE in fish.

  5. The Use of Isotope Techniques to Separate of Hydrography Components. Case Study: Ankara-Guvenc Basin

    International Nuclear Information System (INIS)

    Tekeli, Y.I.; Sorman, A.U.; Sayin, M.

    2002-01-01

    In this research, a stable environmental isotope study was carried out from analysis of water samples collected from rainfall, runoff (total discharge), springs (subsurface flows), and wells (ground waters)in Ankara-Guevenc basin having a drainage area of about 16.125 km 2 between 1996-2000. The aim of the study was to investigate the rainfall-runoff relationship for the basin. Recorded total ten discharge hydrographs are separated to their components using stable isotopes (Oxygen-18, Deuterium) contents. Among these samples, unit hydrographs from two one-peak storm hydrographs were derived using both isotope and graphical methods, and the derived unit hydrographs values including peaks were compared. Peak values of 10 and 20 minutes unit hydrographs of the basin derived by using isotope method (Q p = 1322 1/s and Q p = 1327 l/s) are compared with those of graphical method (Q p = 1656 1/s, and Q p = 1250 1/s) using Barnes semi-log approach. It was found out that, the contribution of subsurface flow which is component of total discharge hydrograph and originating from various sub layers are important in the total flow of basin using isotope method of approach

  6. Scalable and efficient separation of hydrogen isotopes using graphene-based electrochemical pumping

    Science.gov (United States)

    Lozada-Hidalgo, M.; Zhang, S.; Hu, S.; Esfandiar, A.; Grigorieva, I. V.; Geim, A. K.

    2017-05-01

    Thousands of tons of isotopic mixtures are processed annually for heavy-water production and tritium decontamination. The existing technologies remain extremely energy intensive and require large capital investments. New approaches are needed to reduce the industry's footprint. Recently, micrometre-size crystals of graphene are shown to act as efficient sieves for hydrogen isotopes pumped through graphene electrochemically. Here we report a fully-scalable approach, using graphene obtained by chemical vapour deposition, which allows a proton-deuteron separation factor of around 8, despite cracks and imperfections. The energy consumption is projected to be orders of magnitude smaller with respect to existing technologies. A membrane based on 30 m2 of graphene, a readily accessible amount, could provide a heavy-water output comparable to that of modern plants. Even higher efficiency is expected for tritium separation. With no fundamental obstacles for scaling up, the technology's simplicity, efficiency and green credentials call for consideration by the nuclear and related industries.

  7. Separation of rate processes for isotopic exchange between hydrogen and liquid water in packed columns 10

    International Nuclear Information System (INIS)

    Butler, J.P.; Hartog, J. den; Goodale, J.W.; Rolston, J.H.

    1977-01-01

    Wetproofed platinum catalysts in packed columns promote isotopic exchange between counter-current streams of hydrogen saturated with water vapour and liquid water. The net rate of deuterium transfer from isotopically enriched hydrogen has been measured and separated into two rate processes involving the transfer of deuterium from hydrogen to water vapour and from water vapour to liquid. These are compared with independent measurements of the two rate processes to test the two-step successive exchange model for trickle bed reactors. The separated transfer rates are independent of bed height and characterize the deuterium concentrations of each stream along the length of the bed. The dependences of the transfer rates upon hydrogen and liquid flow, hydrogen pressure, platinum loading and the effect of dilution of the hydrophobic catalyst with inert hydrophilic packing are reported. The results indicate a third process may be important in the transfer of deuterium between hydrogen and liquid water. (author)

  8. High-power CO laser with RF discharge for isotope separation employing condensation repression

    Science.gov (United States)

    Baranov, I. Ya.; Koptev, A. V.

    2008-10-01

    High-power CO laser can be the effective tool in such applications as isotope separation using the free-jet CRISLA method. The way of transfer from CO small-scale experimental installation to industrial high-power CO lasers is proposed through the use of a low-current radio-frequency (RF) electric discharge in a supersonic stream without an electron gun. The calculation model of scaling CO laser with RF discharge in supersonic stream was developed. The developed model allows to calculate parameters of laser installation and optimize them with the purpose of reception of high efficiency and low cost of installation as a whole. The technical decision of industrial CO laser for isotope separation employing condensation repression is considered. The estimated cost of laser is some hundred thousand dollars USA and small sizes of laser head give possibility to install it in any place.

  9. Numerical modelling and experimental investigation into zinc isotope separation by laser

    International Nuclear Information System (INIS)

    Bokhan, P.A.; Zakrevskij, D.Eh.; Stepanov, A.Yu.; Fateev, N.V.; Buchanov, V.V.

    2000-01-01

    Experimental research and theoretical modelling of the 66 Zn isotope separation were conducted. Excitation was done through the two-photon process 4s 1 S 0 → 4p 3 P 1 → 6s 3 S 1 on the counter-propagating beams with the small tuning out from the intermediate state. The separation takes place as a result of photochemical reaction by selectively excitation zinc isotope with the CO 2 molecule, which rate is higher by a factors of 3 - 5, than for the unexcited atoms. The experimental investigation into excitation was conducted at the varying parameters of power density and concentration of zinc atoms. The optimum values were found in the process of the investigation. The theoretical basis of possibility for the use of crossed polarization of radiation was carried out [ru

  10. Proceedings of the 2nd specialist research meeting on the electromagnetic isotope separators and their applications

    International Nuclear Information System (INIS)

    Fujioka, Manabu; Kawase, Yoichi; Okano, Kotoyuki

    1992-07-01

    The EMIS-12 International Conference was held at Sendai in September, 1991 for the first time in Japan. It offered a nice opportunity to appeal a great progress in our country on the related fields and many interesting subjects were discussed. The second research meeting on Electromagnetic Isotope Separators and Their Applications was held at Kumatori on March 18 and 19, 1992, six months after the EMIS-12 Conference. Many interesting results obtained by using ISOLs were reported as in the previous meeting. In the present meeting, the measuring methods and the improved instruments were reported and discussed, which are fundamental for application of isotope separation methods to the interdisciplinary research fields. These valuable contributions to the meeting are involved in this Proceedings. (J.P.N.)

  11. Aspects regarding at 13C isotope separation column control using Petri nets system

    International Nuclear Information System (INIS)

    Boca, M L; Ciortea, M E

    2015-01-01

    This paper is intended to show that Petri nets can be also applicable in the chemical industry. It used linear programming, modeling underlying Petri nets, especially discrete event systems for isotopic separation, the purpose of considering and control events in real-time through graphical representations. In this paper it is simulate the control of 13 C Isotope Separation column using Petri nets. The major problem with 13 C comes from the difficulty of obtaining it and raising its natural fraction. Carbon isotopes can be obtained using many methods, one of them being the cryogenic distillation of carbon monoxide. Some few aspects regarding operating conditions and the construction of such cryogenic plants are known today, and even less information are available as far as the separation process modeling and control are concerned. In fact, the efficient control of the carbon monoxide distillation process represents a necessity for large-scale 13 C production. Referring to a classic distillation process, some models for carbon isotope separation have been proposed, some based on mass, component and energy balance equations, some on the nonlinear wave theory or the Cohen equations. For modeling the system it was used Petri nets because in this case it is deal with discrete event systems. In use of the non-timed and with auxiliary times Petri model, the transport stream was divided into sections and these sections will be analyzed successively. Because of the complexity of the system and the large amount of calculations required it was not possible to analyze the system as a unitary whole. A first attempt to model the system as a unitary whole led to the blocking of the model during simulation, because of the large processing times. (paper)

  12. Development of the high temperature ion-source for the Grenoble electromagnetic isotope separator

    International Nuclear Information System (INIS)

    Bouriant, M.

    1968-01-01

    The production of high purity stable or radioactive isotopes (≥ 99.99 per cent) using electromagnetic separation require for equipment having a high resolving power. Besides, and in order to collect rare or short half-life isotopes, the efficiency of the ion-source must be high (η > 5 to 10 per cent). With this in view, the source built operates at high temperatures (2500-3000 C) and makes use of ionisation by electronic bombardment or of thermo-ionisation. A summary is given in the first part of this work on the essential characteristics of the isotope separator ion Sources; a diagram of the principle of the source built is then given together with its characteristics. In the second part are given the values of the resolving power and of the efficiency of the Grenoble isotope separator fitted with such a source. The resolving power measured at 10 per cent of the peak height is of the order of 200. At the first magnetic stage the efficiency is between 1 and 26 per cent for a range of elements evaporating between 200 and 3000 C. Thus equipped, the separator has for example given, at the first stage, 10 mg of 180 Hf at (99.69 ± 0.1) per cent corresponding to an enrichment coefficient of 580; recently 2 mg of 150 Nd at (99.996 ± 0.002) per cent corresponding to an enrichment coefficient of 4.2 x 10 5 has been obtained at the second stage. (author) [fr

  13. Information derived from French studies and achievements in the field of uranium isotope separation

    International Nuclear Information System (INIS)

    Frejacques, C; Galley, R.

    1964-01-01

    The work carried out in the field of uranium isotope separation, by gaseous diffusion and by ultracentrifugation, is reviewed. An economic estimate of the various parameters involved in the cost is given, and it is shown that only very large gaseous diffusion plants, corresponding to a programme of enriched uranium reactors of at least 4000 MWe to be installed yearly, can give an economically acceptable enriched uranium production. (authors) [fr

  14. Tunable lasers in isotope separation, a colorful view of a dye chemist

    International Nuclear Information System (INIS)

    Hammond, P.R.

    1976-01-01

    Some of the problems to be encountered in the large-scale use of dye lasers in an isotope separation plant are discussed. Why should dye lasers be employed. How can dye conversion efficiency be optimized. How can dye photochemical decomposition and hence running costs be minimized and how serious is this effect anyway. What are toxicity problems with the dye. These and similar issues are examined

  15. Analysis and optimization of gas-centrifugal separation of uranium isotopes by neural networks

    Directory of Open Access Journals (Sweden)

    Migliavacca S.C.P.

    2002-01-01

    Full Text Available 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.

  16. The separation and determination of fatty acids by isotopic dilution and radiogas-liquid chromatography

    International Nuclear Information System (INIS)

    Beardsley, D.A.

    1981-01-01

    A number of static phases have been evaluated for the GLC separation of fatty acids. Of those investigated, only AT 1200 was capable of resolving the isomeric forms of the acids. A radiogas-liquid chromatographic method incorporating isotopic dilution analysis has been developed for the determination of n-butyric acid. The proposed method has been applied to the determination of the acid in hydrolysed butter fat and milk chocolate extracts. (author)

  17. High-efficiency technology for lithium isotope separation using an ionic-liquid impregnated organic membrane

    International Nuclear Information System (INIS)

    Hoshino, Tsuyoshi; Terai, Takayuki

    2011-01-01

    The tritium needed as a fuel for fusion reactors is produced by the neutron capture reaction of lithium-6 ( 6 Li) in tritium breeding materials. New lithium isotope separation technique using ionic-liquid impregnated organic membranes (Ionic-Liquid-i-OMs) have been developed. Lithium ions are able to move by electrodialysis through certain Ionic-Liquid-i-OMs between the cathode and the anode in lithium solutions. In this report, the effects of protection cover and membrane thickness on the durability of membrane and the efficiency of isotope separation were evaluated. In order to improve the durability of the Ionic-Liquid-i-OM, we developed highly-durable Ionic-Liquid-i-OM. Both surfaces of the Ionic-Liquid-i-OM were covered by a nafion 324 overcoat or a cation exchange membrane (SELEMION TM CMD) to prevent the outflow of the ionic liquid. It was observed that the durability of the Ionic-Liquid-i-OM was improved by a nafion 324 overcoat. On the other hand, the organic membrane selected was 1, 2 or 3 mm highly-porous Teflon film, in order to efficiently impregnate the ionic liquid. The 6 Li isotope separation factor by electrodialysis using highly-porous Teflon film of 3 mm thickness was larger than using that of 1 or 2 mm thickness.

  18. UNISOR on-line nuclear orientation facility (UNISOR/NOF)

    International Nuclear Information System (INIS)

    Girit, I.C.; Alton, G.D.; Bingham, C.R.; Carter, H.K.; Simpson, M.L.; Cole, J.D.; Croft, W.L.; Hamilton, J.H.; Jones, E.F.; Gore, P.M.; Kormicki, J.; Xie, H.; Kern, B.D.; Krane, K.S.; Xu, Y.S.; Mantica, P.F. Jr.; Zimmermann, B.E.; Nettles, W.G.; Zganjar, E.F.; Kortelahti, M.O.; Newbolt, W.B.

    1988-01-01

    The UNISOR on-line nuclear orientation facility (UNISOR/NOF) consists of a 3 He- 4 He dilution refrigerator on line to the isotope separator. Nuclei are implanted directly into a target foil which is soldered to the bottom accessed cold finger of the refrigerator. A 1.5 T superconducting magnet polarizes the ferromagnetic target foils and determines the axis of symmetry. Up to eight gamma detectors can be positioned around the refrigerator, each 9 cm from the target. A unique feature of this system is that the k=4 term in the directional distribution function can be directly and unambigously deduced so that a single solution for the mixing ratio can be found. The first on-line experiment at this facility reported here was a study of the decay of the 191 Hg and 193 Hg isotopes. (orig.)

  19. Seismic analysis procedures for the plutonium processing building of the Special Isotope Separation Plant

    International Nuclear Information System (INIS)

    Chen, C.P.; Tajirian, F.F.; Todeschini, R.A.A.; Dahlke, H.J.

    1989-01-01

    This paper describes the methodology for the seismic soil-structure interaction (SSI) analysis of the Plutonium Processing Building (PPB) which is part of the Special Isotope Separation (SIS) Production Plant. The PPB consists of two structures, the enclosure building and the optics/separator area. These are founded on two independent foundations which are supported on the surface of a soil medium consisting of gravel overlying basalt. The PPB is classified as a safety related structure and is required to withstand the effects of a Design Basis Earthquake (DBE)

  20. Separation of iodine-131 from water using isotopic exchange with iodine-starch compound

    International Nuclear Information System (INIS)

    Ignatov, V.P.; Kolomejtseva, I.V.

    1990-01-01

    Conditions of iodine isotopic exchange with iodine-starch compound (ISC) were studied with the aim of compound utilizatoin for radioactive iodine separation from solution. It is shown that in pH range from 2 to 7 the degree of iodine extraction and coefficient of its distribution practically do not depend on pH, at pH>7 ISC destruction (decolorizing) starts and iodine extraction decreases. Rapid method of iodine separation from solution is suggested. The method can be used in radiochemical techniques. The degree of extraction equals 80 %, a higher degree of extraction can not be achieved owing to ISC formation peculiarities

  1. Process and device for uranium isotope separation and application for the manufacture of chemical compounds or for the separation of gaseous mixtures otherwise difficult to separate

    International Nuclear Information System (INIS)

    Gregorius, K.; Janner, K.; Kersting, A.; Schuster, E.; Niemann, H.J.

    1987-01-01

    The U235/U238 isotope separation is done by laser excitation with Ur 6 as the initial gaseous material. This has HBr added as the partner for a chemical reaction, preferably in the ratio of 1:10. In order to increase the selectivity and yield, the two partners in the reaction are cooled by adiabatic expansion to below 100 K before irradiation. This makes the absorption bands narrower. The excitation occurs in the Q branch of the rotation vibration spectrum. (DG) [de

  2. Stability of arsenic peptides in plant extracts: off-line versus on-line parallel elemental and molecular mass spectrometric detection for liquid chromatographic separation.

    Science.gov (United States)

    Bluemlein, Katharina; Raab, Andrea; Feldmann, Jörg

    2009-01-01

    The instability of metal and metalloid complexes during analytical processes has always been an issue of an uncertainty regarding their speciation in plant extracts. Two different speciation protocols were compared regarding the analysis of arsenic phytochelatin (As(III)PC) complexes in fresh plant material. As the final step for separation/detection both methods used RP-HPLC simultaneously coupled to ICP-MS and ES-MS. However, one method was the often used off-line approach using two-dimensional separation, i.e. a pre-cleaning step using size-exclusion chromatography with subsequent fraction collection and freeze-drying prior to the analysis using RP-HPLC-ICP-MS and/or ES-MS. This approach revealed that less than 2% of the total arsenic was bound to peptides such as phytochelatins in the root extract of an arsenate exposed Thunbergia alata, whereas the direct on-line method showed that 83% of arsenic was bound to peptides, mainly as As(III)PC(3) and (GS)As(III)PC(2). Key analytical factors were identified which destabilise the As(III)PCs. The low pH of the mobile phase (0.1% formic acid) using RP-HPLC-ICP-MS/ES-MS stabilises the arsenic peptide complexes in the plant extract as well as the free peptide concentration, as shown by the kinetic disintegration study of the model compound As(III)(GS)(3) at pH 2.2 and 3.8. But only short half-lives of only a few hours were determined for the arsenic glutathione complex. Although As(III)PC(3) showed a ten times higher half-life (23 h) in a plant extract, the pre-cleaning step with subsequent fractionation in a mobile phase of pH 5.6 contributes to the destabilisation of the arsenic peptides in the off-line method. Furthermore, it was found that during a freeze-drying process more than 90% of an As(III)PC(3) complex and smaller free peptides such as PC(2) and PC(3) can be lost. Although the two-dimensional off-line method has been used successfully for other metal complexes, it is concluded here that the fractionation and

  3. On-line monitoring of benzene air concentrations while driving in traffic by means of isotopic dilution gas chromatography/mass spectrometry.

    Science.gov (United States)

    Davoli, E; Cappellini, L; Moggi, M; Ferrari, S; Fanelli, R

    1996-01-01

    There is no shortage of information about the average benzene concentrations in urban air, but there is very little about microenvironmental exposure, such as in-vehicle concentrations while driving in various traffic conditions, while refuelling, or while in a parking garage. The main reason for this lack of data is that no analytical instrumentation has been available to measure on-line trace amounts of benzene in such situations. We have recently proposed a highly accurate, high-speed cryofocusing gas chromatography/mass spectrometry (GC/MS) system for monitoring benzene concentrations in air. Accuracy of the analytical data is achieved by enrichment of the air sample before trapping, with a stable isotope permeation tube system. The same principles have been applied to a new instrument, specifically designed for operation on an electric vehicle (Ducato Elettra, Fiat). The zero emission vehicle and the fully transportable, battery-operated GC/MS system provide a unique possibility of monitoring benzene exposure in real everyday situations such as while driving, refuelling, or repairing a car. All power consumptions have been reduced so as to achieve a battery-operated GC/MS system. Liquid nitrogen cryofocusing has been replaced by a packed, inductively heated, graphitized charcoal microtrap. The instrument has been mounted on shock absorbers and installed in the van. The whole system has been tested in both fixed and mobile conditions. The maximum monitoring period without external power supply is 6 h. The full analytical cycle is 4 min, allowing close to real-time monitoring, and the minimum detectable level is 1 microgram/m3 for benzene. In-vehicle monitoring showed that, when recirculation was off and ventilation on, i.e., air from outside the vehicle was blown inside, concentrations varied widely in different driving conditions: moving from a parking lot into normal traffic on an urban traffic condition roadway yielded an increase in benzene concentration

  4. The Institute for Cryogenics and Isotope Separation - History, Present and Prospective

    International Nuclear Information System (INIS)

    Stefanescu, Ioan

    1998-01-01

    The foundation of plant 'G' at Rm. Valcea on March 1, 1970 has opened a technological prospect within the Romania Program of Nuclear Energy Development and led to formation of a school of experts under supervision of professor Marius Peculea, the Secretary general of Romanian Academy. The fruitful scientific activity of the plant's staff in approaching advanced technologies of heavy water separation resulted in numerous valuable technical solutions, patents and know-hows of national interest as well as a great number of scientific works which today constitutes a useful information basis for all the personnel engaged in the organization and growth of industrial production of heavy water. The research work continued by approaching new methods of hydrogen isotope separation, by initiation of selective physical adsorption of gases in porous materials, in the high vacuum techniques as well as in the technologies of low and very low temperatures. Following this scientific progress and based on the results of scientific research and technological developments, in 1996 the National Institute of Research-Development for Cryogenics and Isotopic Technologies, ICSI, at Rm. Valcea was founded. Research - development activity of ICSI is undertaken within the frames of several research programs at the science-technology interface. A special attention was paid to developing cryogenics, technologies and equipment specific for tritium and deuterium separation as well as the production and turning to account the gases and gas mixtures for industrial or laboratory applications. In ICSI two facilities of national interest operate, one in a stage of maintenance - the heavy water pilot and the other in current operation - the experimental pilot for tritium and deuterium separation. The outstanding target of ICSI is to become an internationally competitive institute in the field of cryogenic equipment and technologies specific to isotope separation, boosting the technological transfer to

  5. Improvements to the on-line mass separator, RAMA, and the beta-delayed charged-particle emission of proton-rich sd shell nuclei

    International Nuclear Information System (INIS)

    Ognibene, T.J.

    1996-03-01

    To overcome the extreme difficulties encountered in the experimental decay studies of proton drip line nuclei, several techniques have been utilized, including a helium-jet transport system, particle identification detectors and mass separation. Improvements to the ion source/extraction region of the He-jet coupled on-line Recoil Atom Mass Analyzer (RAMA) and its target/ion source coupling resulted in significant increases in RAMA efficiencies and its mass resolution, as well as reductions in the overall transit time. At the 88-Inch Cyclotron at LBNL, the decays of 31 Cl, 27 P and 28 P, with half-lives of 150 msec, 260 msec and 270.3 msec, respectively, were examined using a he-jet and low-energy gas ΔE-gas ΔE-silicon E detector telescopes. Total beta-delayed proton branches of 0.3% and 0.07% in 31 Cl and 27 P, respectively, were estimated. Several proton peaks that had been previously assigned to the decay of 31 Cl were shown to be from the decay of 25 Si. In 27 P, two proton groups at 459 ± 14 keV and 610 ± 11 keV, with intensities of 7 ± 3% and 92 ± 4% relative to the main (100%) group were discovered. The Gamow-Teller component of the preceding beta-decay of each observed proton transition was compared to results from shell model calculations. Finally, a new proton transition was identified, following the β-decay of 28 P, at 1,444 ± 12 keV with a 1.7 ± 0.5% relative intensity to the 100% group. Using similar low-energy detector telescopes and the mass separator TISOL at TRIUMF, the 109 msec and 173 msec activities, 17 Ne and 33 Ar, were studied. A new proton group with energy 729 ± 15 keV was observed following the beta-decay of 17 Ne. Several discrepancies between earlier works as to the energies, intensities and assignments of several proton transitions from 17 Ne and 33 Ar were resolved

  6. Early evaluation of hydrogen isotopes separation by V4Cr4Ti-based sorbents at low temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Kulsartov, Timur, E-mail: tima@physics.kz [Institute of Experimental and Theoretical Physics of Kazakh National University, 050038 Almaty (Kazakhstan); Institute of Atomic Energy of National Nuclear Center, 071100 Kurchatov (Kazakhstan); Shestakov, Vladimir; Chikhray, Yevgen; Kenzhina, Inesh; Askerbekov, Saulet [Institute of Experimental and Theoretical Physics of Kazakh National University, 050038 Almaty (Kazakhstan); Gordienko, Yuriy; Ponkratov, Yuriy; Zaurbekova, Zhanna [Institute of Atomic Energy of National Nuclear Center, 071100 Kurchatov (Kazakhstan)

    2016-12-15

    This paper presents the results of experiments on hydrogen isotopes sorption with V4Cr4Ti vanadium alloys from a mixture of hydrogen isotopes. The studies were carried out at temperatures of 353 K, 393 K, 423 K; and pressures of 10{sup 3}–10{sup 4} Pa in gas mixture of hydrogen isotopes. The α-phase domain of V-H (D) system was studied, where the concentration of hydrogen isotopes atoms should not exceed 0.015H (D) atoms per metal atom. The separation parameters were derived for several saturation conditions accordingly to registered time dependences of hydrogen isotopes partial pressure drop. The conclusion was made about the prospects of using vanadium alloys in hydrogen isotopes separation and purification systems.

  7. Identification of new proton-rich rare earth nuclei by means of the coupled system helium jet-isotope separator of SARA

    International Nuclear Information System (INIS)

    Ollivier, T.

    1986-01-01

    In order to study new exotic nuclei far from stability we built a fast separation system by coupling a helium jet with the medium-current source of the mass separator. First the tests were made in Lyon and then the system used on line with the heavy ion accelerator SARA, in Grenoble. We obtained efficiency greater than 1% for each element and a better chemical independence. This allowed us to perform experiments on rare-earth region near N=82, with fusion-evaporation reactions after an investigation of various ranges of beam energies. The first results allow to identify two new isotopes, 143 Tb (12s) and 138 Eu (12s). The decay schemes obtained are analysed in the frame of existing models [fr

  8. Separation of uranium and plutonium isotopes for measurement by multi collector inductively coupled plasma mass spectroscopy

    International Nuclear Information System (INIS)

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

    2009-01-01

    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 233 U and 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 R column coupled to a UTEVA R 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 234 U/ 235 U, 238 U/ 235 U, 236 U/ 235 U, and 240 Pu/ 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. (author)

  9. Simulation and optimization of stable isotope 18O separation by water vacuum distillation

    International Nuclear Information System (INIS)

    Chen Yuyan; Qin Chuanjiang; Xiao Bin; Xu Jing'an

    2012-01-01

    In the research, a stable isotope 18 O separation column was set up by water vacuum distillation with 20 m packing height and 0.1 m diameter of the column. The self-developed special packing named PAC- 18 O was packed inside the column. Firstly, a model was created by using the Aspen Plus software, and then the simulation results were validated by test results. Secondly, a group of simulation results were created by Aspen Plus, and the optimal operation conditions were gotten by using the artificial neural network (ANN) and Statistica software. Considering comprehensive factors drawn from column pressure and from withdrawing velocity, conclusions were reached on the study of the impact on the abundance of the isotope 18 O. The final results show that the abundance of the isotope 18 O increases as column pressure dropping and withdrawing velocity decreasing. Besides, the optimal column pressure and the incidence formula between the abundance of the isotope 18 O and withdrawing velocity were gotten. The conclusion is that the method of simulation and optimization can be applied to 18 O industrial design and will be popular in traditional distillation process to realize optimization design. (authors)

  10. Design of a formaldehyde photodissociation process for carbon and oxygen isotope separation

    International Nuclear Information System (INIS)

    Stern, R.C.; Scheibner, K.F.

    1993-01-01

    The current shortage of 18 O has revived interest in using one step UV photodissociation of formaldehyde to enrich 13 C, 17 O and 18 O. The frequency doubled output of the copper laser pumped dye laser system currently in operation at LLNL can be used to drive this dissociation. The authors use a simple kinetics model and their experience with Atomic Vapor Laser Isotope Separation (AVLIS) process design to examine the relative merits of different designs for a formaldehyde photodissociation process. Given values for the molecular photoabsorption cross section, partition function, spectroscopic selectivity, collisional exchange and quenching cross sections (all as parameters), they perform a partial optimization in the space of illuminated area, formaldehyde pressure in each stage, and formaldehyde residence time in each stage. They examine the effect of cascade design (heads and tails staging) on molecule and photon utilization for each of the three isotope separation missions, and look in one case at the system's response to different ratios of laser to formaldehyde costs. Finally, they examine the relative cost of enrichment as a function of isotope and product assay. Emphasis is as much on the process design methodology, which is general, as on the specific application to formaldehyde

  11. Electrochemical separation and isotopic determination of thallium at the nanogram level by surface ionisation mass spectrometry

    International Nuclear Information System (INIS)

    Arden, J.W.

    1983-01-01

    A rapid low-blank procedure is described for the co-separation of thallium and lead by sequential cathodic and anodic electrodeposition from natural samples, especially complex natural silicates, for subsequent mass spectrometry. A micro anion-exchange procedure is also described for the separation of thallium and lead. Ion currents of 10 - 10 A can be obtained from 1 ng of thallium. The isotopic composition of 1 ng of thallium can be measured on a Faraday detector with a precision of 0.05-0.1%. The total procedural blank is 3 pg. By using stable isotope dilution, 0.2 ng of thallium can be measured with a precision of 0.6% with only a 2% blank correction. This allows the accurate determination of thallium in natural samples down to concentration levels of about 50 pg g - 1 . The detection limit is 50 fg. This procedure has been applied to meteorites and terrestrial rocks. The stable isotope dilution technique is suitable for geochemical, environmental and toxicological studies requiring a highly sensitive, accurate and precise method for the determination of thallium. (Auth.)

  12. Study of the isotopic exchange associated with ionic exchange for the radiochemical separation of 233-Th

    International Nuclear Information System (INIS)

    Sepulveda Munita, C.J.A.

    1983-01-01

    The isotopic ion exchange procedure is applied in order to establish an analytical method for the determination of thorium by means of the 233 Th activity, when the presence of interfering elements does not allow a direct non-destructive activation analysis. The separation is based on the retention of 233 Th by a thorium saturated resin, due to the isotopic exchange effect, and subsequent elution of the interfering radioisotopes with a solution of thorium in diluted hydrochloric acid. The interfering elements were those which either present a great affinity for the resin or emit gamma rays with energies close to that of 233 Th (86.6 KeV), when a NaI(Tl) detector is used to obtain the gama-ray spectra of the irradiated samples. The equilibrium time for the thorium isotopic ion exchange and the distribution coefficients for the interfering elements were determined by using Bio-Rad AG 50W resins (100-200 mesh), with 4% to 8% of divinylbenzene. The best separation conditions were established in terms of the thorium and hydrochloric acid concentrations in the solution, the resin cross-linking degree, and the solution flow through the resin. The analytical method was applied to the determination of thorium in samples of ammonium diuranate as well in standard rock samples from the United States Geological Survey. The sensitivity, precision and accuracy of the method are also discussed. (Author) [pt

  13. Separation of isotopes of nitrogen and oxygen by low temperature distillation of nitrogen oxide

    Energy Technology Data Exchange (ETDEWEB)

    Isomura, Shohei; Tonooka, Yasuhiko; Kaetsu, Hayato

    1987-02-01

    In general, the distillation parameters, such as the number of theoretical plate (NTP) and the height equivalent to a theoretical plate (HETP), can be obtained from the operation at the steady state. However, it is time-consuming to achieve the steady state especially in the case of isotope separation. In this paper, with the purpose of simultaneous separation of isotopes of nitrogen and oxygen by NO distillation, we tried to determine the distillation parameters by an analytical method through the transient-state operation. It was confirmed that the results from the analysis were in good agreement with those observed for the operation at the steady state. Enrichment of the isotopes was carried out using a distillation column with a height of 1 m and inside diameter of 12 mm. The dependence of HETP on liquid flow rate was measured by the proposed method. The obtained HETP values were from 2 to 4 cm. The operation time of about 5 h was found to be long enough to determine the distillation parameters.

  14. Separation of isotopes of nitrogen and oxygen by low temperature distillation of nitrogen oxide

    International Nuclear Information System (INIS)

    Isomura, Shohei; Tonooka, Yasuhiko; Kaetsu, Hayato

    1987-01-01

    In general, the distillation parameters, such as the number of theoretical plate (NTP) and the height equivalent to a theoretical plate (HETP), can be obtained from the operation at the steady state. However, it is time-consuming to achieve the steady state especially in the case of isotope separation. In this paper, with the purpose of simultaneous separation of isotopes of nitrogen and oxygen by NO distillation, we tried to determine the distillation parameters by an analytical method through the transient-state operation. It was confirmed that the results from the analysis were in good agreement with those observed for the operation at the steady state. Enrichment of the isotopes was carried out using a distillation column with a height of 1 m and inside diameter of 12 mm. The dependence of HETP on liquid flow rate was measured by the proposed method. The obtained HETP values were from 2 to 4 cm. The operation time of about 5 h was found to be long enough to determine the distillation parameters. (author)

  15. Modeling of filling gas centrifuge cascade for nickel isotope separation by feed flow input to different stages

    Directory of Open Access Journals (Sweden)

    Orlov Alexey A.

    2017-01-01

    Full Text Available The article presents results of research filling gas centrifuge cascade by process gas fed into different stages. The modeling of filling cascade was done for nickel isotope separation. Analysis of the research results shows that nickel isotope concentrations of light and heavy fraction flows after filling cascade depend on feed stage number.

  16. Determination of Cd, Hg, Pb and Se in sediments slurries by isotopic dilution calibration ICP-MS after chemical vapor generation using an on-line system or retention in an electrothermal vaporizer treated with iridium

    International Nuclear Information System (INIS)

    Vieira, Mariana Antunes; Ribeiro, Anderson Schwingel; Dias, Lucia Felicidade; Curtius, Adilson Jose

    2005-01-01

    A method for the determination of Cd, Hg, Pb and Se in sediments reference materials by slurry sampling chemical vapor generation (CVG) using isotopic dilution (ID) calibration and detection by inductively coupled plasma mass spectrometry (ICP-MS) is proposed. Two different systems were used for the investigation: an on-line flow injection system (FI-CVG-ICP-MS) and an off-line system with in situ trapping electrothermal vaporization (CVG-ETV-ICP-MS). About 100 mg of the reference material, ground to a particle size ≤50 μm, was mixed with acid solutions (aqua regia, HF and HCl) in an ultrasonic bath. The enriched isotopes 111 Cd, 198 Hg, 206 Pb and 77 Se were then added to the slurry in an adequate amount in order to produce an altered isotopic ratio close to 1. For the on-line system, a standing time for the slurry of 12 h before measurement was required, while for the batch system, no standing time is needed to obtain accurate results. The conditions for the formation of the analyte vapor were optimized for the evaluated systems. The following altered isotope ratios were measured: 111 Cd/ 114 Cd, 198 Hg/ 199 Hg, 206 Pb/ 208 Pb e 77 Se/ 82 Se. The obtained detection limits in the on-line system, in μg g -1 , were: Cd: 0.15; Hg: 0.09; Pb: 6.0 and Se: 0.03. Similar detection limits were obtained with the system that uses the ETV: 0.21 for Hg, 6.0 for Pb and 0.06 μg g -1 for Se. No signal for Cd was obtained in this system. One estuarine, two marine and two river certified sediments were analyzed to check the accuracy. The obtained values by both systems were generally in agreement with the certified concentrations, according to the t-test for a confidence level of 95%, demonstrating that isotope equilibration was attained in the slurries submitted to a chemical vapor generation procedure and detection by ICP-MS. The relative standard deviations were lower than 10%, adequate for slurry analysis. The almost quantitative analytes extractions to the aqueous phase

  17. Study of the coefficient of separation for some processes which are applied to lithium isotopes; Etude du coefficient de separation de quelques processus concernant les isotopes du lithium

    Energy Technology Data Exchange (ETDEWEB)

    Perret, L.; Rozand, L.; Saito, E. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1958-07-01

    The fundamental separation factors of some processes are investigated: the distillation of metallic lithium, counter current electromigration in fused salts (particularly in lithium nitrate) electrolysis in aqueous solution and ion exchange. The chemical transfer between a lithium amalgam and lithium salts in a dimethylformamide solution (a solvent which is not attacked by the amalgam) is also studied. Finally a description is given of isotopic analyses carried out either by scintillation counting or by mass spectrography using apparatus specially designed for this particular task. (author) [French] Les facteurs de separation elementaires de quelques processus connus sont etudies: distillation du lithium metallique, electromigration a contre-courant en sels fondus (en particulier le nitrate), electrolyse en solution aqueuse et echange d'ions. L'echange chimique entre l'amalgame de lithium et les sels de lithium en solution dans la dimethylformamide - solvant non attaque par l'amalgame - est egalement etudie. Enfin, on decrit les methodes d 'analyse isotopique, soit par comptage par scintillation, soit par spectrometrie de masse au moyen d'un appareil specialement concu pour cet usage particulier. (auteur)

  18. Study of the coefficient of separation for some processes which are applied to lithium isotopes; Etude du coefficient de separation de quelques processus concernant les isotopes du lithium

    Energy Technology Data Exchange (ETDEWEB)

    Perret, L; Rozand, L; Saito, E [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1958-07-01

    The fundamental separation factors of some processes are investigated: the distillation of metallic lithium, counter current electromigration in fused salts (particularly in lithium nitrate) electrolysis in aqueous solution and ion exchange. The chemical transfer between a lithium amalgam and lithium salts in a dimethylformamide solution (a solvent which is not attacked by the amalgam) is also studied. Finally a description is given of isotopic analyses carried out either by scintillation counting or by mass spectrography using apparatus specially designed for this particular task. (author) [French] Les facteurs de separation elementaires de quelques processus connus sont etudies: distillation du lithium metallique, electromigration a contre-courant en sels fondus (en particulier le nitrate), electrolyse en solution aqueuse et echange d'ions. L'echange chimique entre l'amalgame de lithium et les sels de lithium en solution dans la dimethylformamide - solvant non attaque par l'amalgame - est egalement etudie. Enfin, on decrit les methodes d 'analyse isotopique, soit par comptage par scintillation, soit par spectrometrie de masse au moyen d'un appareil specialement concu pour cet usage particulier. (auteur)

  19. Electrolytic separation factors for oxygen isotopes in light and heavy water solutions

    International Nuclear Information System (INIS)

    Gulens, J.; Olmstead, W.J.; Longhurst, T.H.; Gale, K.L.; Rolston, J.H.

    1987-01-01

    The electrolytic separation factor, α, has been measured for /sup 17/O and /sup 18/O at Pt and Ni anodes in both light and heavy water solutions of 6M KOH as a function of current density. For oxygen-17, isotopic separation effects were not observed, within the experimental uncertainty of +-2%, under all conditions studied. For oxygen-18, there is a small difference of 2% in α values between Pt and Ni in both light and heavy water solutions, but there is no significant difference in α values between light and heavy water solutions. In light waters solutions, the separation factor at Pt is small, α(/sup 18/O) ≤ 1.02 for i ≥ 0.1 A/cm/sub 2/. This value agrees reasonably well with theoretical estimates

  20. The momentum-loss achromat - a new method for the isotopical separation of relativistic heavy ions

    International Nuclear Information System (INIS)

    Schmidt, K.H.; Geissel, H.; Muenzenberg, G.; Dufour, J.P.; Hanelt, E.

    1987-03-01

    The application of the slowing-down process of relativistic heavy ions in a layer of matter in ion-optical devices is theoretically investigated. The modifications of the phase space of the ion beam due to the dissipative forces and the straggling phenomena are discussed. Methods are developed to study the properties of the momentum-loss achromat, an isotope separator consisting of an achromatic magnetic system with an energy degrader located in the intermediate dispersive focal plane. This device separates projectile fragments with respect to A and Z up to uranium over a wide energy range with an efficiency in the order of 50% and with separation times of several hundred nanoseconds. (orig.)