The indicated methods for determining the following constituents of Diban, which is an aqueous solution of dibasic aluminum nitrate, Al(OH)2NO3, were evaluated statistically: 1aluminum by gravimetric, volumetric, and spectrophotometric procedures, 2. basicity (hydroxyl value) by formation of an aluminum complex and titration of the free acid with standard alkali solution, 3. total nitrogen by the Kjeldahl method, 4. ammonia by the Kjeldahl method, and 5. nitrates by means of a cation-exchange resin and titration of the liberated acid with standard alkali solution. Recommendations are made regarding the preferred methods of determining the constituents in dibasic aluminum nitrate and regarding means of minimizing errors in these analyses.

Several plates of 98.7% Th - 1.2% U 235 (clad in aluminum) were irradiated in the MTR for an integrated flux of 2.6 x 10 21 neutrons/cm2. Although these samples represent an early development in bonding of aluminum to thorium and there are better methods at present, the bond proved to be quite strong and both clad and core were dimensionally stable under irradiation. The production of uranium 233 was as much as theory would indicate and the total amount of fissionable material material after irradiation and after decay of the protactinium 233 was greater than before irradiation. A fuel element of this nature appears to offer excellent potentialities from the standpoint of radiation stability.

This report presents data obtained from processing 33 Clementine Reactor fuel elements in the ORNL Metal Recovery Plant to recover approximately 15 kg of plutonium and 0.16 g of americium.

LITR Fluoride-Fuel Loop. — The inconel loop was dismantled for removal of the samples and for recovery of the uranium by using the remote cutting tools installed in a half cell of the Solid State Building. Disassembly proceeded without incident. An electric-arc cutting technique was developed for removal of the stainless steel enclosure around the pump bowl. Fission power and maximum flux were determined by irradiating a simulated loop, by heat-balance calculations, by radiochemical analyses for fission products in the fuel, by measuring the activation of cobalt foils attached to the loop, and by activation of the loop tubing itself. The determination of the power by these various methods gave 2.5 to 2.8 kw during operation of the loop, and the maximum power density was 0.4 kw/cc. Chemical analyses of the fuel were carried out to determine U, Zr, and the major constituents of inconel: Ni, Cr, and Fe.

An ion-exchange -- polarographic method was developed for the determination of iron(III) in Homogeneous Reactor Fuels. Copper, which interferes, is removed from the fuel by plating it onto a cadmium coil. Iron is oxidized to iron(III) by potassium permanganate, and the iron(III) is separated from interfering metal ions by ion exchange on a Dowex 1 resin column that is in the sulfate form. The iron(III) in the effluent is determined polarographically in 0.5 M sodium citrate solution as supporting electrolyte. A fairly well defined polarographic wave is obtained for the iron(III) → iron(II) reduction at a half-wave potential of approximately -0.15 v. vs. the S.C.E. The relative standard deviation of the data for 2 µg of iron(III) per ml of solution in the polarographic cell was 6.5%; for 10 µg of iron(III) per ml it was 0.6%.

Diffusion in an arc plasma across a magnetic field is investigated. The geometry is similar to that reported in ORNL-1890 but with the addition of magnetic mirrors on the ends of the arc chamber. It is shown that mirrors do not eliminate the "short circuit" effect. Comparison of the e-folding length, rₒ, of the radial ion density with and without mirrors, affords a direct measurement of ℓ/λ where ℓ is the arc length and λ the mean-free-path. In addition rₒ is independent of gas pressure with mirrors and varies as √p without mirrors. The condition for the elimination of the "short circuit" effect is discussed, as well as the case in which the "short circuit" is still present but the ions diffuse (rather than stream) to the end walls. In this case rₒ is directly proportional to the gas pressure. These effects are compared to some experimental results of Neidigh

The development of ionic methods for the determination of corrosive products in the highly radioactive Homogeneous Reactor (HR) fuels has been of major interest in the work of the Ionic Analyses Laboratory. Methods for the spectrophotometric determination of aluminum and for the polarographic determination of iron in HR fuels have been developed. The polarographic determination of molybdenum in uranyl sulfate solutions was studied. A polarographic method for the determination of zinc was developed. A fluorometric method for the determination of microgram amounts of fluoride was studied. Three organic reagents were investigated as precipitants for microgram quantities of zirconium in HR fuel. The automatic photometric titration technique was applied to the determination of thorium and of sulfate. A method was developed for the ion-exchange separation and potentiometric titration of cobalt. The ultraviolet absorption spectra of technetium and rhenium were studied.

An evaluation of the relative health hazards of radioisotopes produced in nuclear reactors is reported. The most important hazards were indicated to be I131, the Sr90 - Y90 chain, the Ce144 -Pr144 chain, Sr 89, the Ba140-La40 chain, Y91, the Zr95-Nb95 chain, Pr143, La140 , and Pa233. The most critical body organs affected by air-borne contamination are the thyroid gland, the bone marrow, the lungs, and the gastrointestinal tract. Where possible, continuous daily removal of gaseous and solid fission products from the reactor environment can be shown to permit very significant reductions in the total hazards. Homogeneous reactors, such as the Thermal Breeder Reactor and the Homogeneous Plutonium Producer Reactor, specifically studied in this report, are designed with daily removal cycles and may be considered potentially safer than heterogeneous reactors.

A direct titrimetric method for the determination of trivalent uranium in uranium trifluoride and mixtures of fused fluoride salts was developed. The method is based on the stoichiometric oxidation of trivalent uranium to the tetravalent oxidation state with an acidic solution of methylene blue. The sample containing trivalent uranium is dissolved at room temperature in an excess of standard methylene blue solution in a carbon dioxide atmosphere; the excess oxidant is variation of the method is 1.5 per cent for 5 mg quantities of trivalent uranium. The method was applied to various mixtures of fluoride salts containing both trivalent and tetravalent uranium.

From July 7 to August 31, 1955, 20 tons of uranium and 1,200 g of plutonium were recovered in 47 days of plant operation at an average rate of 833 lb/day of uranium and at a cost of $2.60/lb of uranium. Uranium and plutonium recoveries were, respectively, 99.9 and 95.5 per cent.

This memorandum is the first in a series reporting progress in the program of critical experiments in the ORNLArmy Package Power Reactor Project. The critical assembly, designated as CA-25, is analogous to the APPR design core and consists of 45 fuel boxes, in a 7 x 7 array with the corners removed, contaIned in a large water tank. Two sides of each box are slotted for the insertion and positioning of any desired loading of eighteen plates of fuel, structural material, and poison. The array is submerged in water to provide a moderated and reflector. Enriched uranium metal, in two-mil-thick foils 2.5 x 22 in, is encased in type 304 stainless steel sheets, 2.7 x 23 x 0.0105 in., to form fuel plates. Stainless steel plates, 2.7 x 23 x 0.025 in. are used to simulate additional steel in the APPR core. It is, therefore, possible to maintain an essentially constant metal to water ration in the assembly when the fuel content is varied. The fuel is distributed as uniformly as possible in all boxes and a symmetrical distribution of materials is maintained in the core at all times. Fuel plates containing half-width (1.25 in) uranium foils are provided for …

The Spectroscopy Research Laboratory is concerned with research and development in the fields of nuclear magnetic resonance, microwaves, infrared and optical spectroscopy, spectrochemistry, and x rays. Research is directed toward fruitful methods of isotope analysis; new element and compound analytical methods having application to immediate Laboratory or long-range commission needs; and fundamental research on isotopes, elements, and compounds. The work is reported on a project basis to give a more complete picture of the purpose, activity, and status of each program. More detailed information on reported or inactive projects may be obtained from the previous semiannual report.

The successful completion of a program of experiments, including the Aircraft Reactor Experiment (ARE), has demonstrated the high probability of producing militarily useful aircraft nuclear power plants employing reflector-moderated circulating-fuel reactors. Consequently, and accelerated program culminating in operation of the Aircraft Reactor Test (ART) is under way. In order to adhere to the compressed schedule of the accelerated program, it is essential that the Atomic Energy Commission approve the 7500 Area in Oak Ridge as the test site by February15, 1955. This report summarizes the hazards associated with operating the contained 60-Mv reactor of the ART at the proposed Oak Ridge test site.

From July through December, a total of 1750 hr of computer time was used by programmers in "debugging" and in running problems. With the acquisition of a second operator, the evening shift was initiated. A night-shift operator is presently being trained, and third-shifts operations will probably begin after completion of the magnetic-tape memory. / Engineering time is regularly scheduled for 4 hr each morning and 1/2 hr late in the afternoon. An electronic technician is on duty during evening-shift operations. / Installations of the magnetic-tape memory units is complete, and the units are expected to go into operation in the near future. Work is continuing on the new input-output system.

The reactor equipment cell is expected to be completed by February 15. While filled with water, the tank was inspected for leaks, and the few leaks found will have been repaired by February 15. All orders for construction materials placed prior to this quarter have been received. New requisitions issued during the quarter total $16,000. Work orders were issued, and fabrication of all low-pressure-system components was begun in the ORNL shops. The thermal shield around the reactor vessel was specified as a 2-ft-thick cylindrical concrete wall. With this shield, the fast-neutron flux in the equipment area will be reduced to 7 x 109 neutrons/cm2/sec, the slow flux to 4 x 107 neutrons/cm2/sec, and the gamma intensity to less than 105 r/hr. The possible blast effects from a rupture of the pressure vessel were studied and are judged to be sufficient to justify the inclusion of a 1.5. to 2-in.-thick blast shield around the pressure vessel. The blast shield eliminates the danger of damaging the leak tight equipment-cell liner. Pressures in the reactor equipment cell, as a result of vessel failure, were calculated in order to arrive at a safe design pressure for the reactor equipment cell. For the case of …

The ORNL 86-in. cyclotron is being modified to provide for deflection of the proton beam. It is expected that operation will be resumed late in the spring. Nuclear physics work was limited, for the most part, to interpretation of previously collected data and to making preparations for utilizing the deflected beam. It was found that for certain isotopes the production rates could be almost doubled by operating at a slightly reduced energy and a much larger current. With the use of the ORNL 63-in. cyclotron, the absolute values of the electron capture and loss cross sections for 26-Mev nitrogen ions were obtained. The angular distribution of the cross sections for elastic scattering of nitrogen by nitrogen was measured at energies from 13 to 22 Mev. A double-focusing 90-deg magnet is being planned for use in identifying stable reaction products from nitrogen-induced reactions. The major components of the revised 44-in. test cyclotron were assembled and are being tested. Consideration is being given to the use of these components, along with a new 20,000-oersted magnet and a shielded cyclotron room, and if the tests are satisfactory the Laboratory will have available a machine which will accelerate N5+ ions to 81 Mev.

A satisfactory ion-exchange-polarographic method was developed for the determination of either chromium(VI) or total chromium in Homogeneous Reactor fuels. Total chromium is determined as chromium (VI) , i.e., chromate, and in the same way as is chromium(VI), after chromium in the lower valence states is oxidized to chromate by potassium permanganate. Chromate is separated from all interfering metal ions in the fuel by ion exchange on a Dowex 50 resin column. The Chromate in the effluent is determined polarographically in approximately 0.75 M sodium hydroxide solution as supporting electrolyte. A well polarographic wave is obtained for the chromium (VI) chromium (III) reduction at a half-wave potential of -0.85 volt vs. the S.C.E. The relative standard deviation of the data for 2 μg of chromium (VI) per ml was 2%; for 4 μg of total chromium per ml, it was 3%. An ion-exchange-polarographic method was developed also for the determination of chromium(III). Chromium (III) is separated from all interfering ions in the fuel by ion exchange on a Dowex 1 resin column. The chromium (III) in the effluent is determined polarographically in a 1M ammonia-1M ammonium chloride supporting electrolyte. The wave obtained at a half-wave potential of -1.42 volt vs. the …

Part I. Experimental Reactors: The effect of prompt-neutron lifetime upon reactor safety was investigated for the HRT. It was found that for a given pressure rise the allowable rate of reactivity addition was relatively insensitive to the average prompt-neutron lifetime, although the rate de creased somewhat with decreasing lifetime for the higher pressure rises. With only source neutrons present and the reactor initially subcritical, the allowable rate was practically independent of the initial value of k£. For a core-pressure rise of 400 psi, the corresponding rate of reactivity addition was about 0.8% per second; for a pressure rise of 4000 psi, the rate was 2.5 to 3.0% per second. Part II. Thorium Breeder Reactor: An economic study of one-region thorium breeder reactors was completed. Where possible, the process characteristics and cost factors were the same as those used previously in studies of two-region-type reactors. The mini mum-cost reactor is about 12 ft in diameter, operating with 260 g of thorium per liter on a chemical processing cycle of about 450 days. The ratio of U232 to U233 produced is approximately 2 x 10~4 VIM in the minimum-cost one-region system, compared with 4 x 10 5 in the two-region system. The …

Bench scale studies have been made of the recovery of uranium from acid leach liquors (and slurries) by solvent extracting with di (2-ethylhexyl) phosphoric acid in an organic diluent. Uranium may be stripped from the organic solvent by either alkaline or acidic reagents, the former having been studied in greater detail. On the basis of these tests, a recovery process may be considered which shows promise both from the standpoint of operation and chemical costs. Under proper conditions, vanadium can also be extracted by the di (2-ethylhexyl) phosphoric acid and stripping again may be accomplished with either acidic or alkaline reagents. Preliminary studies have been made of these possibilities. In addition to di (2-ethylhexyl) phosphoric acid, some other organophosphorus acids, have been cursorily examined in respect to their extraction and/or stripping performance.

Report containing papers, publications, and announcements from the Physics Division of the Oak Ridge National Laboratory.

Report containing papers, publications, and announcements from the Solid State Division of the Oak Ridge National Laboratory.

Report that contains descriptions of the electronic equipment used with the multiple-crystal gamma-ray spectrometer.

A capital cost breakdown of the Idaho Chemical Processing Plant, a directly maintained remotely operated plant for processing spent enriched uranium fuel assemblies from reactors, is presented. The capital investment in the plant, including design, construction, training, and preoperational costs, an estimate of the direct costs incurred by the Atomic Energy Commission, and a proportional part of the costs of Central Facilities, including the value of the land and improvements theorem when acquired by the Commision, was $31,105,899. The cost of design and construction was $25,212,231, of which $3,773,357 was expanded on design and inspection.

Construction of the HRT reactor shield tank was completed, and the inside surfaces were painted. The roof structure for the tank is being assembled in preparation for an acceptance pressure test. Service piping and instrument lines are being installed in the central room area by ORNL craft forces. This work is approximately 50% complete. Fabrication of all temperature system components, except the blanket outer storage tanks, has been completed.