Abstract: Isotopes of either germanium or silicon are separated by a chemical exchange reaction. Preferably the compound is a hydro halide or halide composition and the donor can be a wide variety of compounds such as a lower molecular weight alcohol.

Abstract: A method for selectively photoionizing odd mass Zr atoms. Atomic vapours are subjected to two resonant laser pulses to raise the energy of Zr atoms from the J=2 ground state, to a J=1 first intermediate state and to a second intermediate state prior to ionization. Quantum mechanical selection rules applicable to linearly polarized light and hyperfine interactions are exploited to produce odd mass selectivity.

Abstract: A method and apparatus for the partial or complete continuous separation of isotopes of gadolinium, especially high thermal neutron capture cross-section gadolinium isotopes, using continuous, steady-state, chromatography in which an ion exchange resin is the stationary phase, an aqueous solution of ions based on a mixture of gadolinium isotopes is the feed phase, and an aqueous acid eluant solution is the mobile phase. The method involves the mobile phase eluting or desorbing the gadolinium isotopic solute or ligand adsorbed on the stationary phase under conditions such that each of the various naturally occurring isotopes of gadolinium is primarily eluted in an elution volume distinct from the elution volumes of the other isotopes. In a preferred embodiment, the conditions are such that at least one of the elution volumes contains essentially only one isotope of gadolinium.

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

Abstract: This invention relates to a process of and apparatus for the continuous and selective separation of boron-10 (B.sup.10) isotope having high neutron capture cross-section from boron-11 (B.sup.10) isotope from a mixture of boron isotopes in a boric acid solution by using a weak base ion exchange resin and water eluant in a continuous annular chromatograph.

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

Abstract: Methods and apparatus for producing selenium-72, separating it from its daughter isotope arsenic-72, and generating multiple portions of a solution containing arsenic-72 from a reusable parent substance comprised of selenium-72. The invention provides apparatus which can be located at a site where arsenic-72 is used, for purposes such as PET imaging, to produce arsenic-72 as needed, since the half-life of arsenic-72 is very short.

Abstract: A method for selectively photoionizing odd mass Zr atoms. Atomic vapours are subjected to three resonant and are non resonant laser pulses to raise the energy of Zr atoms from the J=2 ground state, to a J=1 first intermediate state, to a J=(second intermediate state and to a third intermediate state prior to ionization.

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

Abstract: Disclosed is an efficient biological process for recovering heavy metals from refractory manganiferous ore, and a process for removing heavy metal contaminants from the soil. The process utilizes manganese reducing Bacillus sp. Specifically exemplified is a novel microbe designated Bacillus MBX 69, or mutants thereof, and the known microbe Bacillus polymyxa, which is disclosed in U.S. Pat. No. 5,055,130. Further, gene(s) encoding the enzyme(s) obtainable from the said bacteria can be used by placing such gene(s) on a suitable vector and transforming a competent host. The transformed host then can be used in the same manner as the native microbe. Also, the enzyme(s) themselves can be used in the above-described processes.

Abstract: The thermal neutron capture cross-section of zirconium may be altered by altering its natural isotope distribution through a steady state chromatographic separation of these isotopes using an anion exchange resin as the stationary phase of the chromatographic column. Zirconium is dissolved in a very strong acid which causes the formation of a zirconium anion, such as the ZrOCl.sub.4.sup.-2 anion formed in six normal hydrochloric acid, and eluted off the column with a weaker acid. Distinct elution volumes representative of each isotope are collected. In a preferred embodiment, the process also separates the zirconium from hafnium and the other impurities normally present in the product obtained by chlorinating zircon sand and utilizes a continuous annular chromatograph.

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

Abstract: The isotopes of zirconium can be partially or completely separated by loading an aqueous solution of an ionic compound of zirconium onto a cationic exchange resin with pentavalent phosphorus derived active groups which serves as the stationary phase of a chromatograph, eluting the compound with an aqueous acid and collecting distinct elution volumes representative of each isotope. In a preferred embodiment, the eluant is a strong mineral acid, such as hydrochloric acid and the chromatograph is of a type, such as a continuous annular chromatograph, that it can be operated in a continuous, steady state manner.

Abstract: A new type of RL light source consisting of a zeolite crystalline material, the intralattice spaces of which a tritiated compound and a luminophore are sorbed, and which material is optionally further dispersed in a refractive index-matched polymer matrix.

Abstract: The isotopes of zirconium can be partially or completely separated by loading an aqueous solution of an ionic compound of zirconium onto a cationic exchange resin which serves as the stationary phase of a chromatograph, eluting the compound with an aqueous acid and collecting distinct elution volumes representative of each isotope. In a preferred embodiment, the eluant is a strong mineral acid, such as hydrochloric acid and the chromatograph is of a type, such as a continuous annular chromatograph that it can be operated in a continuous, steady state manner.

Abstract: The present invention relates to a process and apparatus for purifying waste gases by scrubbing with an adsorbent suspension. The adsorbent suspension in a concentration from 40 g/l to 200 g/l is here distributed uniformly or almost uniformly in at least one gas-scrubbing device, passed through at least one ordered mass transfer zone and contacted with the gas and then passed into at least one separately arranged reactor, the biologically degradable or convertible impurities are reacted, with the additional use of aerobic bacteria and oxygen, with forced motion and the purified liquid or suspension is recycled, wholly or as part stream, to the gas-scrubbing device, distributed therein and contacted again with the gas which is to be purified.

Abstract: A method for concentrating an isotope from an admixture containing the isotope by contacting the admixture with a catalyst capable of selectively catalyzing a reaction with the isotope, and recovering the concentrated isotope from the reaction products. In one embodiment, the method can be used to concentrate deuterium from sources such as hydrogen-rich gas.

Abstract: Tritium and deuterium are separated from a gaseous mixture thereof, derived from a nuclear fusion reactor or some other source, by providing a casing with a bulk getter therein for absorbing the gaseous mixture to produce an initial loading of the getter, partially desorbing the getter to produce a desorbed mixture which is tritium-enriched, pumping the desorbed mixture into a separate container, the remaining gaseous loading in the getter being deuterium-enriched, desorbing the getter to a substantially greater extent to produce a deuterium-enriched gaseous mixture, and removing the deuterium-enriched mixture into another container. The bulk getter may comprise a zirconium-aluminum alloy, or a zirconium-vanadium-iron alloy. The partial desorption may reduce the loading by approximately fifty percent. The basic procedure may be extended to produce a multistage isotope separator, including at least one additional bulk getter into which the tritium-enriched mixture is absorbed.

Abstract: A gas-gas phase contactor/process, especially adopted for high temperature reactions, e.g., for the production of hydrochloric acid, comprises means for separately establishing at least two disparate gaseous feedstreams, means for disintegrating each such feedstream into a registered plurality of substreams thereof, one of each such substream being complementary to at least one eother, and means for establishing homogeneous unit volumes of gaseous reaction mixture which comprise said complementary fractions of each such disintegrated feedstream.

Abstract: There is provided a generator for short-lived radionuclides. The generator comprises a support, an ion-exchange agent and a parent radionuclide in a steady-state equilibrium with a daughter nuclide, which daughter nuclide can be selectively eluted from said column. A suitable parent radionuclide is .sup.191 OS in equilibrium with .sup.191m Ir. There is also provided a specific Os(VI) complex which has certain advantages.

Abstract: A process for the wet calcination of sodium bicarbonate, sodium sesquicarbonate or mixtures thereof comprising forming a suspension of sodium bicarbonate, sodium sesquicarbonate or said mixture in a water-immiscible relative high boiling liquid, and heating the suspension to form sodium carbonate.

Abstract: A method and apparatus for separation of an isotope mixture of hydrogen, sting predominantly in molecular form and/or inbound form, from the remaining components of a gas. A first chamber is separated from a second chamber by a wall which is permeable for atomic hydrogen and less permeable for molecular hydrogen. The hydrogen is converted into atomic hydrogen or, if necessary, is separated in atomic form from the material with which the hydrogen has gone into chemical composition. A device electrically operable independently of the wall is provided for converting the molecular and/or bound hydrogen to form atomic hydrogen in apparatus for this purpose. A heating device for elevating the temperature of thread, wire, or body of other form capable of being heated above 1500 K is provided and such thread, wire, or body is made of high-melting material, such as tungsten, iridium, osmium, or rhenium.

Abstract: Use of succinosuccinic acid diesters of the formula ##STR1## in which R is an alkyl, alkenyl or cycloalkyl having 4 to 24 C atoms, either dissolved in a water-immiscible organic solvent, or at elevated temperature in the form of their melts, as cation-selective liquid membranes.

Abstract: A method for the separation of the isotopes of carbon comprising contacting an aqueous solution containing an acid-dissociated type chemical species of a carbon-containing acid and a non-dissociated type chemical species of said acid with an anion exchange resin as a solid phase, thereby to allow an isotope exchange reaction with respect to carbon to proceed between said acid-dissociated type chemical species and said non-dissociated type chemical species and, concurrently, to adsorb said acid-dissociated type chemical species on said anion exchange resin, and separate C.sup.12 and C.sup.13 respectively into a solution phase and the solid phase or the solid phase and a solution phase, whereby C.sup.13 is concentrated. This method can be practised at an extremely favorable efficiency and inexpensive cost, as compared with the prior art method for the separation utilizing a distillation method or a chemical exchange method between gas--liquid phases, gas--solution phases, solution--solution phases and the like.

Abstract: A method of separating isotopes of hydrogen which comprises subjecting a ture of methane and isotopes of hydrogen in a methane to hydrogen mole ratio from about 1000:1 to about 1:10 to a glow electrical discharge from about 10.sup.-3 to about 50eV per hydrogen bond at a temperature from about 50.degree. K. to about 310.degree. K. and at a pressure from about 0.3 Torr to the pressure at which arcing occurs.