4,795 research outputs found

    Electrically Conductive Paints for Satellites

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    A program was conducted to develop and test electrically conductive paint coatings for spacecraft. A wide variety of organic and inorganic coatings were formulated using conductive binders, conductive pigments, and similar approaches. Z-93, IITRI's standard specification inorganic thermal control coating, exhibits good electrical properties and is a very space-stable coating system. Several coatings based on a conductive pigment (antimony-doped tin oxide) in silicone and silicate binders offer considerable promise. Paint systems using commercially available conductive polymers also appear to be of interest, but will require substantial development. Evaluations were made based on electrical conductivity, paint physical properties, and the stability of spectral reflectance in space environment testing

    Method of preparing zinc orthotitanate pigment

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    Zinc orthotitanate suitable for use as a pigment for spacecraft thermal control coatings is prepared by heating a slightly zinc deficient reaction mixture of precipitated oxalates of zinc and titanium. The reaction mixture can be formed by coprecipitation of zinc and titanium oxalates from chloride solution or by mixing separately precipitated oxalates. The mixture is first heated to 400 to 600 C to remove volatiles and is then rapidly heated at 900 to 1200 C. Zinc orthotitanate produced by this method exhibits the very fine particle size needed for thermal control coatings as well as stability in a space environment

    The extraction of uranium from brannerite

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    Brannerite, UTi2O6 is the most important uranium mineral after uraninite, UO2 and coffinite, U(SiO4)1-x(OH)4x. It is also the most common refractory uranium mineral. Ores containing brannerite typically require intense conditions (>50 g/L H2SO4, >75°C) compared to other uranium ores for effective uranium extraction to occur. To develop an effective process for the extraction of uranium from brannerite containing ores and improve the extraction from the ores currently being processed, it is necessary to understand the chemistry of the brannerite leaching process. As this study has shown, brannerite is typically an altered and amorphous mineral, with an extent of alteration depending on the age of the sample and the geological history of the deposit. A sample of brannerite from Cordoba, Spain, was leached over a range of conditions in acidic ferric sulphate media. The sample was filled with cracks and altered zones containing anatase (TiO2). Process parameters studied included temperature (25-96°C), acidity (10-200 g/L H2SO4) and the effect of adding selected gangue minerals (apatite, fluorite and ilmenite). The feed and the leached residues were characterised in detail by XRD and SEM-EDX techniques. The results of this study showed that brannerite dissolution has a stronger dependence on temperature and lesser dependence on free acid concentration. Comparisons between the residues and the feed showed that the altered and amorphous areas of the brannerite sample are more readily leached than crystalline areas. The crystalline areas of the brannerite dissolved congruently, with titanium subsequently precipitating as anatase physically separated from the original brannerite grains

    Leaching of brannerite in the ferric sulphate system — Part 1: Kinetics and reaction mechanisms

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    The uranium titanate mineral brannerite, UTi2O6 is the most common of the uranium minerals which is considered refractory. Ore containing brannerite mineralisation has been mined and processed in several locations around the world. Under typical uranium ore processing conditions, brannerite is often lost to tailings. In order to design an effective process for the leaching of high-brannerite uranium ores, it is first necessary to understand the mechanism of the chemical processes through which brannerite dissolves in the absence of interferences from the host rock. In the present study, a specimen of brannerite obtained as a single crystal was leached in sulphuric acid (10-200 g/L) and ferric sulphate (2.8 g/L Fe3 +) solution at 25-96°C for 5 h. The rate of titanium dissolution was monitored along with uranium. Comparisons between the rates at which these two elements dissolved and the morphological changes that were observed to take place during the dissolution process indicated two different sets of leaching reaction mechanisms. At low temperatures, uranium dissolved at a much higher rate than titanium initially, leaving titanium rich areas on the brannerite particles similar to observations reported in earlier investigations which suggest incongruent dissolution. The calculated activation energies for uranium and titanium dissolution were 36 and 48 kJ/mol respectively. At higher temperatures, uranium and titanium dissolved at similar rates in constant proportions suggesting congruent dissolution. The calculated activation energy for this reaction was 23 kJ/mol. The transition between incongruent and congruent dissolution took place at lower temperatures when the acid concentration was higher. Titanium appeared to undergo hydrolysis after dissolution, forming anatase. This side reaction was most favourable at lower acid concentrations and high temperatures

    Development of space stable thermal control coatings for use on large space vehicles

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    The evaluation and environmental testing of zinc orthotitanate pigments for use as space stable thermal control coatings on large space vehicles are discussed. Electron paramagnetic resonance spectra of the pigments and their precursor compounds are examined. A continuing study of the spectral intensity of mercury-argon and mercury-xenon sources in reported. Results of long term environmental testing of commercially available, strippable, protective coatings are discussed

    Development of a space stable thermal control coatings for use in large space vehicles

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    The preparation and evaluation of zinc orthotitanate and of several new pigments and the environmental testing and evaluation of these pigments and of coatings made from them constitute the bulk of the work accomplished. New pigments were prepared and EPR spectra of pigments and their precursor compounds studied. Results of extensive testing of commercially-available, strippable, protective coatings are reported; Owens-Illinois 650 glass resin has been stabilized against progressive mechanical failures; and definite improvements have been noted. A zinc oxide pigmented lithium silicate paint has demonstrated very good ultraviolet stability

    Distribution and Relative Abundance of Butterflyfishes and Angelfishes Across a Lagoon and Barrier Reef, Andros Island, Bahamas

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    Juveniles of Chaetodon capistratus, C. striatus, C. ocellatus, C. sedentarius, Pomacanthus arcuatus, P. paru, Holacanthus ciliaris, and H. tricolor occurred in the shallow lagoon habitats. Adults and subadults of these species were associated with the deeper barrier reef and seaward platform habitats. C. aculeatus occurred only on the outer seaward platform. In strip transects at a seaward platform site, C. capistratus and H. tricolor were found with significantly greater abundance than P. paru and C. striatus

    Hyper-Fractionated Radiotherapy for Soft Tissue Sarcoma: Results of the Second Study of Hyper-Fractionated Radiotherapy

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    Purpose and Method. Hyper-fractionated radiotherapy for treatment of soft tissue sarcomas is designed to deliver a higher total dose of radiation without an increase in late normal tissue damage. In a previous study at the Royal Marsden Hospital, a total dose of 75 Gy using twice daily 1.25 Gy fractions resulted in a higher incidence of late damage than conventional radiotherapy using 2 Gy daily fractions treating to a total of 60 Gy. The current trial therefore used a lower dose per fraction of 1.2 Gy and lower total dose of 72 Gy, with 60 fractions given over a period of 6 weeks

    Chemical stability of zirconolite for proliferation resistance under conditions typically required for the leaching of highly refractory uranium minerals

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    In this study, synthetic zirconolite samples with a target composition Ca0.75Ce0.25ZrTi2O7, prepared using two different methods, were used to study the stability of zirconolite for nuclear waste immobilisation. Particular focus was on plutonium, with cerium used as a substitute. The testing of destabilisation was conducted under conditions previously applied to other highly refractory uranium minerals that have been considered for safe storage of nuclear waste, brannerite and betafite. Acid (HCl, H2SO4) leaching for up to 5 h and alkaline (NaHCO₃, Na2CO3) leaching for up to 24 h was done to enable comparison with brannerite leached under the same conditions. Ferric ion was added as an oxidant. Under these conditions, the synthetic zirconolite dissolved much slower than brannerite and betafite. While the most intense conditions were observed previously to result in near complete dissolution of brannerite in under 5 h, zirconolite was not observed to undergo significant attack over this timescale. Fine zirconolite dissolved faster than the coarse material, indicating that dissolution rate is related to surface area. This data and the long term stability of zirconolite indicate that it is a good material for long-term sequestration of radioisotopes. Besides its long term durability in the disposal environment, a wasteform for fissile material immobilisation must demonstrate proliferation resistance such that the fissile elements cannot be retrieved by leaching of the wasteform. This study, in conjunction with the previous studies on brannerite and betafite leaching, strongly indicates that the addition of depleted uranium to the wasteform, to avert long term criticality events, is detrimental to proliferation resistance. Given the demonstrated durability of zirconolite, long term criticality risks in the disposal environment seem a remote possibility, which supports its selection, above brannerite or betafite, as the optimal wasteform for the disposition of nuclear waste, including of surplus plutonium
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