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1.
This study investigates how estimates of uranium endowment made by a geologist using an appraisal system that is based upon a formalization of geoscience and decision rules compare with estimates made by informal and unconstrained intuitive processes. The motivation for this study derives from the premise that formalization of decisions would mitigate the heuristic biases and hedging that may result from the use of unconstrained intuitive processes. Estimates of the uranium endowment of the San Juan Basin of New Mexico by four methodologies are compared in this study. These methods, ranked from top to bottom by degree of decomposition (mitigating of heuristic bias)and control on hedging, are as follows Implicit 2 1.5 × 106 s.t. of U3O8 Implicit 1 1.6 × 106 s.t. of U3O8 NURE (1980) 2.4 × 106 s.t. of U3O8 Appraisal system 3.9 × 106 s.t. of U3O8 The magnitude of expected uranium endowment estimated by these methods, ranked from smallest to largest, is in this same order. With the exception of the NURE estimates, the magnitude of the variance (uncertainty)of uranium endowment, ranked from smallest to largest, also is in this same order. These results prompt the suggestion that the more decomposed and formalized the estimation procedure, the greater the expected value and the variance of uranium endowment. Equivalently, predicating U 3 O 8 endowment estimation strictly upon that part of the geologist's geoscience that is useful in making U 3 O 8 endowment estimates and upon his understanding of the region's history produced larger estimates than have previously been reported. However, this method of estimation also shows that uncertainty about the actual state of U 3 O 8 endowment is much greater than previously described.  相似文献   

2.
Several radioactive anomalies due to uranium and thorium, associated with the mesedimentary enclaves (Archaean) within granite (Archaean to Early-Proterozoic) have been recorded in parts of Karimnagar Granulite Terrain, Karimnagar Dist. At Peddur and Kottur, Uraninite has been identified in the samples of metasediments. The metasediment from these two places have been subjected to granulite facies of metamorphism and host high values of uranium with negligible thorium. In Peddur, samples of metasediments have assayed as high as 1.96% U3O8 with negligible thorium, and in Kottur up to 0.059% U3O8. Leaching studies on these samples have indicated that most of the U3O8 present is leachable. This discovery has opened up the possibility of finding uranium mineralisation in Archaean metasediments and thus provides a thrust for uranium exploration in similar geological environs in India. Further, the basement granite along with the metasedimentary enclaves has the potential to act as a provenance for a possible unconformity type or sandstone type U-deposit in the rocks of overlying Pakhal and Gondwana Supergroup, in Pranhita-Godavari Basin, situated to the east of this area.  相似文献   

3.
    
This study investigates how estimates of uranium endowment made by a geologist using an appraisal system that is based upon a formalization of geoscience and decision rules compare with estimates made by informal and unconstrained intuitive processes. The motivation for this study derives from the premise that formalization of decisions would mitigate the heuristic biases and hedging that may result from the use of unconstrained intuitive processes. Estimates of the uranium endowment of the San Juan Basin of New Mexico by four methodologies are compared in this study. These methods, ranked from top to bottom by degree of decomposition (mitigating of heuristic bias)and control on hedging, are as follows Implicit 2 1.5 × 106 s.t. of U3O8 Implicit 1 1.6 × 106 s.t. of U3O8 NURE (1980) 2.4 × 106 s.t. of U3O8 Appraisal system 3.9 × 106 s.t. of U3O8 The magnitude of expected uranium endowment estimated by these methods, ranked from smallest to largest, is in this same order. With the exception of the NURE estimates, the magnitude of the variance (uncertainty)of uranium endowment, ranked from smallest to largest, also is in this same order. These results prompt the suggestion that the more decomposed and formalized the estimation procedure, the greater the expected value and the variance of uranium endowment. Equivalently, predicating U 3 O 8 endowment estimation strictly upon that part of the geologist's geoscience that is useful in making U 3 O 8 endowment estimates and upon his understanding of the region's history produced larger estimates than have previously been reported. However, this method of estimation also shows that uncertainty about the actual state of U 3 O 8 endowment is much greater than previously described. Paper presented at the 10th Geochautauqua: Computer Applications in the Earth Sciences, 23–24 October 1981, Ottawa, Canada.  相似文献   

4.
A new method for accurate determination of oxygen isotopes in uranium oxides encountered in the nuclear fuel cycle was developed using the conventional BrF5 fluorination technique. Laser‐assisted fluorination was tested for comparison. We focused on fine powders of triuranium octoxide (U3O8), uranium dioxide (UO2±x with 0 ≤ x ≤ 0.25), uranium trioxide (UO3.nH2O, with 0.8 ≤ n ≤ 2) and diuranates (M2U2O7.nH2O, with M = NH4, Na or Mg0.5 and 0 ≤ n ≤ 6). Fluorination at room temperature and heating under vacuum at 150 °C are shown to eliminate both adsorbed and structural water from the powder samples. Precision fit for purpose of δ18O values (± 0.3‰, 1s) and oxygen yields (close to 100%) were obtained for U3O8 and UO2 where oxygen is only bound to uranium. A lower precision was observed for UO3.nH2O and M2U2O7.nH2O where oxygen is both present in the structural H2O and bonded to uranium and where the extracted O2(g) can be contaminated by NF3 and NOx compounds. Laser‐assisted fluorination gave shifted δ18O values between +0.8 and +1.4‰ for U3O8, around ?0.8‰ for UO3.nH2O and between ?3.9 and ?4.5‰ for M2U2O7.nH2O (± 0.3‰, 1s) compared with the conventional method.  相似文献   

5.
X-ray diffraction (XRD) studies on the radioactive ore samples from various parts of Rajasthan and Haryana have revealed the presence of several uranium and other atomic mineral occurrences in the albitite belt of western India. The primary uranium minerals (PUMs) are uraninite and brannerite, whereas, the secondary uranium minerals (SUMs) show considerable speciations: phosphate, silicate, hydrous oxide hydrate, and vanadate. Multiple oxides (MOs) are davidite, fergusonite, aeschynite-(Y), microlite, samarskite, euxenite, betafite, and columbite-tantalite. The thorium minerals are huttonite, thorite, uranoan-thorite, thorianite, thorutite, and brabantite. The yttrium and REE-bearing minerals are xenotime, britholite, allanite, chevkinite, tritomite, and monazite. It is noted that the measured unit cell dimension (a0) of the investigated uraninites ranges from 5.4110 Å to 5.4646 Å. The highest unit cell dimension (5.4646 Å) represents a composition (or oxidation grade) of UO2.05, whereas, the lowest one (5.4110 Å) corresponds to a composition of UO2.54. Furthermore, it is also apparent that, with increase in oxidation grade, there is a concomitant decrease in unit cell dimension. As most of the values of ao of uraninites from the albitite belt are high (> 5.45 Å), it may be inferred that the overall temperature of formation of uraninites of the albitite belt was higher (ca. 400°C). However, the low values of a0 in certain localities could be due to the prevalence of relatively low and fluctuating temperature regimes locally (ca. 400°–100° C). Numerous occurrences of refractory, multiple oxides, and REE minerals, in association with uranium mineralisation, also support a high-temperature origin for the investigated uraninites. Binary data plots of unit cell dimension (a0) versus oxidation grade/composition (UO2+x) of uraninites (n = 36) suggest that the gross uranium mineralisation in the albitite belt of western India is mainly linked to regional metamorphism, anatexis, granitic intrusion, metasomatism, and contact metamorphosed granite-pegmatite aureoles and granite-related vein type with hydrothermal overprints, including redistribution of intrinsic sedimentary uranium and its concentration along suitable structural locales. These interpretations are consistent with the known gross geologic features of the albitite belt. Furthermore, the presence of marialite (calcian) in many places in the albitite belt also supports such a contention, as this mineral is known to be restricted to metamorphic and metasomatic environments. The speciation of secondary uranium minerals could be due to the higher oxidation of U4+ to U6+ in surface to near-surface conditions and its (U6+) remobilisation as uranyl ions. The combination of moving uranyl ions with available cations and anions en route caused re-precipitation of U as diversified assemblages of low-temperature uranyl minerals under suitable physicochemical conditions.  相似文献   

6.
Magnetic properties are reported for the spinel series Fe2.4—t Cr0.6Ti t O4, 0≦t≦0.7, with t=0, 0.2, 0.4, 0.6 and Fe2.1—t Cr0.9Ti t O4, 0≦t≦0.55, with t=0, 0.2, 0.4, 0.45, 0.5. Magnetic moment data are compared with theoretical values derived from different ion distribution models. With increasing Ti concentration the compositions become hard magnetic spinels due to the increased number of Fe2+ ions on A- and B-sites of the spinel lattice.  相似文献   

7.
Mineralisation of uraninite and brannerite occurs in the albitised metasedimentary and intrusive igneous rocks of Kerpura-Tiwari-ka-bas area in Sikar district, Rajasthan. Samples collected from well dumps contain 0.016 to 1.52% U3O8 with very low ThO2. The host rocks show wide variation in chemical composition due to varying degree of alkali metasomatism, associated alteration and composition of protoliths. The spatial distribution of uranium in groundwater as well as rock samples from well dumps indicates localisation of the uranium mineralisation along NNE-SSW and NWSE directions in Kerpura block. Petrographic and lithogeochemical studies point towards close genetic relationship between alkali metasomatism and uranium mineralisation. The mineralisation seems to be due to mobilisation of uranium and other LILEs by metasomatising fluids and their deposition along shear zones at a later stage, which may not be spatially related to zones of intense albitisation.  相似文献   

8.
An attempt has been made in Chinnar sub basin of Dharmapuri district, South India to isolate the geochemistry of uranium occurrences in groundwater. The geology of the area is mainly of charnockite and granite gneiss. Groundwater samples were collected for two different seasons post and pre monsoon in two different litho units (granite gneiss and charnockite) and analysed for major, minor and uranium concentrations. Higher uranium (18.45 μg L?1) has been recorded during pre monsoon season in granite gneiss with increasing pH. The saturation index calculation for the groundwater isolated minerals like uaraninite, coffinite, haiweeite and soddyite to be precipitating and uranium oxides like UO2.25, UO2.25beta, UO2.33beta as oversaturated. The Eh-pH diagram attempted represents solubility of uraninite within the pH range of 6.0 to 8.0. The study isolate uranium in groundwater of the study area is controlled by the presence of (U4O9) uranium oxide.  相似文献   

9.
林子瑜  聂逢君  张士红  徐翅翔  余倩 《地质通报》2019,38(11):1867-1876
兰杰一号铀矿及其所属的鳄鱼河铀矿田产于北澳太古宙克拉通内古元古代裂谷背景下发展起来的松溪造山带,矿体产于新太古代—古元古代结晶-变质基底/晚古元古代—中元古代康博尔吉红层建造不整合界面之下,铀矿化分3个时代,U_1为1720～1680Ma,U_2为1420～1040Ma,U_3为474±6Ma,U1是主矿化时代。该矿床于1969年后期通过航空放射性测量被发现,1970’s经勘探圈定了No.1和No.3两个铀矿体,总计资源储量124681t@0.23%U_3O_8。1980年10月正式露采,至2018年12月,总计生产了128739t U_3O_8。1985财年开始,ERA(澳大利亚能源资源有限责任公司)向世界核能市场共计销售了产于兰杰铀矿的119882t U_3O_8。2009年,发现了No.3深部矿,探明资源储量为43857t@0.22%U_3O_8,这部分资源将以地下开采方式利用。预计到2026年,采区地貌景观和生态环境将得到恢复。进一步讨论了澳北元古宙不整合面型铀矿找矿的方向,持续稳定的铀矿开采与生产的意义,以及投资澳大利亚铀矿业需要注意的政治与法律问题。这些内容可以为国内矿业企业及地勘单位合理部署澳洲铀矿勘查与开发提供参考。  相似文献   

10.
By means of paramagnetic Mössbauer spectra the cation distribution of the solid solution CoFe x Al2?x O4 with 0≦x≦1.5 has been determined. The existence of high field magnetic susceptibility at low temperature for samples with x≧0.4 has been interpreted in terms of non-collinear ferrimagnetic arrangements. Below the Neel temperature the spinel CoAl2O4 has a complex antiferromagnetic behavior.  相似文献   

11.
Computational and experimental studies were performed to explore heterogeneous reduction of U6+ by structural Fe2+ at magnetite (Fe3O4) surfaces. Molecular Fe-Fe-U models representing a uranyl species adsorbed in a biatomic bidentate fashion to an iron surface group were constructed. Various possible charge distributions in this model surface complex were evaluated in terms of their relative stabilities and electron exchange rates using ab initio molecular orbital methods. Freshly-cleaved, single crystals of magnetite with different initial Fe2+/Fe3+ ratios were exposed to uranyl-nitrate solution (pH ∼ 4) for 90 h. X-ray photoelectron spectroscopy and electron microscopy indicated the presence of a mixed U6+/U5+ precipitate heterogeneously nucleated and grown on stoichiometric magnetite surfaces, but only the presence of sorbed U6+ and no precipitate on sub-stoichiometric magnetite surfaces. Calculated electron transfer rates indicate that sequential multi-electron uranium reduction is not kinetically limited by conductive electron resupply to the adsorption site. Both theory and experiment point to structural Fe2+ density, taken as a measure of thermodynamic reducing potential, and sterically accessible uranium coordination environments as key controls on uranium reduction extent and rate. Uranium incorporation in solid phases where its coordination is constrained to the uranate type should widen the stability field of U5+ relative to U6+. If uranium cannot acquire 8-fold coordination then reduction may proceed to U5+ but not necessarily U4+.  相似文献   

12.
We show evidence that the primary uranium minerals, uraninite and coffinite, from high-grade ore samples (U3O8>0.3%) in the Wuyiyi, Wuyier, and Wuyisan sandstone-hosted roll-front uranium deposits, Xinjiang, northwestern China were biogenically precipitated and psuedomorphically replace fungi and bacteria. Uranium (VI), which was the sole electron acceptor, was likely to have been enzymically reduced. Post-mortem accumulation of uranium may have also occurred through physio-chemical interaction between uranium and negatively-charged cellular sites, and inorganic adsorption or precipitation reactions. These results suggest that microorganisms may have played a key role in formation of the sandstone- or roll-type uranium deposits, which are among the most economically significant uranium deposits in the world.  相似文献   

13.
The Baxingtu deposit is a typical redox front tabular-shaped uranium deposit hosted in sandstones of the Late Cretaceous Yaojia Formation deposited within a braided river environment during the post-rift stage of the Songliao Basin, in northeast China. This study proposes the first metallogenic model for the Baxingtu deposit and provides new data on genetic processes involved in the uranium mineralisation of sandstone-type deposits that were characterised through petrographic observations, whole-rock geochemistry, and geochemical and/or mineralogical study of iron disulphide, uranium minerals, Fe-Ti oxides (EPMA, LA-ICP-MS), and organic matter (REP). The δ34S value has been measured in situ by SIMS on the different generations of iron disulphide.Within regional primary reduced sandstones, pre-ore uranium enrichment (Umean = 7.6 ppm in whole rock) was identified on altered Fe-Ti oxides along with minor concentrations on organic matter (respectively 26.3% and 1.3% of the whole-rock U content), which together represent a significant source of uranium for the mineralisation. Additional pre-ore uranium concentrations may also be associated with clay minerals. Petrographic observations and REP data indicate that organic matter occurring in the host-sandstone is mainly inherited from land plants and corresponds to type III or type IV kerogens. Ore-stage iron disulphides largely occur as framboids and in replacement of organic matter or also as sub-idiomorphic to idiomorphic cement and crystal. Trace element signatures detected within framboids are likely indicative of formation mainly from a single event. Framboids and iron disulphide in replacement of organic matter have a light sulphur isotope signature characterised by δ34S values from −72.0 to −6.2‰, suggesting that sulphur originated from bacterial sulphate reduction, which was mainly responsible for (1) the liberation of U from Fe-Ti oxides and organic matter, (2) the generation of ore-stage iron disulphides, (3) the bioreduction of uranium and (4) the production of a secondary H2S-rich reducing barrier also involved in uranium reduction. Uranyl and sulphate ions were transported through the host sandstone by low-temperature oxygenated groundwater and U(IV) was precipitated at the redox interface as nano to microcrystals of pitchblende and coffinite, dominantly associated with bacterial substrate and as intergrowth with biogenic iron disulphide or directly associated with organic matter and residual Ti-Fe oxides. The uranium mineralisation does not replace ore-stage iron disulphides. Therefore, the combined mineralogical, geochemical, and isotopic characteristics of the Baxingtu tabular uranium deposit characterise dominantly biogenic processes for the genesis of the uranium mineralisation.  相似文献   

14.
The interactions of humic substances from Esthwaite Water with hydrous iron oxides (α-FeOOH, α-Fe2O3, amorphous Fe-gel) have been examined by measuring adsorption isotherms and by microelectrophoresis. In Na+-Cl?-HCO3?at I = 0.002 M (medium I) the extent of adsorption decreases with increasing pH. The results are consistent with a mechanism involving ligand exchange of humic anionic groups with H2O and OH?of surface Fe-OH2+and Fe-OH groups respectively, with an increasing degree of protonation of the adsorbed humics as the adsorption density increases at constant pH.At pH 7 in a medium containing Mg2+, Ca2+ and SO42?, at their Esthwaite Water concentrations and at I= 0.002 M (medium II) the adsorption capacity of goethite (α-FeOOH) is approximately twice that in medium I. Electrophoresis experiments show that the extra capacity is associated with coadsorption of Mg2+ and/or Ca2+ ions.When the iron oxides are added to samples of Esthwaite Water itself they become negatively charged and plots of electrophoretic mobility against pH for the natural water are identical to those in medium II plus humics.  相似文献   

15.
Dolostone of Vempalle Formation near Tummalapalle hosts large uranium deposit (>100,000 tonnes with an average grade of 0.045%U3O8). It is a unique type of uranium deposit because carbonate formations have been considered to be among the least uraniferous of all the rocks of the Earth’s crust due to mobility of uranium in aqueous fluid in the presence of carbonate and bicarbonate ions. Vempalle dolostone hosts syn-sedimentary uranium mineralization in the form of discrete uranium phases (pitchblende and coffinite) associated with collophane, and adsorbed uranium in organic matter. The organic matter has played dual role of concentrating uranium from solution and also chemically reducing it to pitchhblende and coffinite.  相似文献   

16.
Black shale type uranium deposits, though of low grade (<0.001 to 0.05% U3O8), contain large uranium resources because of their immense volume. The Neoproterozoic-Cambrian Krol-Tal Himalayan sequence covering a cumulative area of about 1000 sq km in five different synclinal basins from Sirmour district, Himachal Pradesh in the west to Nainital district, Uttar Pradesh in east contain such black shale horizons. The uranium mineralisation found in black shale in the Nigalidhar syncline of Himachal Pradesh and its implication of being an indicator for search of such uranium deposits in Himalayas is discussed.  相似文献   

17.
The southeastern part of the Nanling metallogenic province, China is host to numerous granite-hosted vein-type hydrothermal uranium deposits. The geology and geochemistry of these deposits have been extensively studied. However, accurate and precise ages for the uranium mineralization are scarce because the uranium minerals in these deposits are usually fine grained, and may have formed in several stages. Therefore, the ages previously obtained by the bulk dating techniques are possibly a mixed age.The Xianshi uranium deposit, located in the southeastern part of the Guidong granite complex, is a major uranium deposit in South China. The uranium mineralization from this deposit is mainly fine grained uraninite in quartz or calcite veins which are spatially associated with the Cretaceous mantle-derived mafic dykes. Micro-Raman spectroscopy and X-ray diffraction analyses indicate that the dominant uranium mineral occurs as a rare form of uraninite (U3O7). Three distinct generations of uranium minerals have been identified based on petrographic and field relations. Stage 1 uraninite has the lowest UO2 and highest PbO contents whereas Stage 3 uraninite has the highest UO2 and lowest PbO contents.Uraninite from the Xianshi deposit was dated using an in-situ SIMS U–Pb dating technique. The results show three distinct age groups: 135 ± 4 Ma, 113 ± 2 Ma and 104 ± 2 Ma, which are in excellent agreement with the ages of three episodes of mantle-derived mafic dykes. Therefore, the Xianshi uranium deposit has experienced at least three hydrothermal events that are responsible for the deposition of uranium ores, which are genetically related to the emplacement of three sets of mafic dykes.  相似文献   

18.
We studied the role of microbial photosynthesis in the oxidation of Fe(II) to Fe(III) in a high Fe(II) and high Mn(II) hot spring devoid of sulfide and atmospheric oxygen in the source waters. In situ light and dark microelectrode measurements of Fe(II), Mn(II) and O2 were made in the microbial mat consisting of cyanobacteria and anoxygenic photosynthetic Chloroflexus sp. We show that Fe(II) oxidation occurred when the mat was exposed to varying intensities of sunlight but not near infrared light. We did not observe any Mn(II) oxidation under any light or dark condition over the pH range 5-7. We observed the impact of oxygenic photosynthesis on Fe(II) oxidation, distinct from the influence of atmospheric O2 and anoxygenic photosynthesis. In situ Fe(II) oxidation rates in the mats and cell suspensions exposed to light are consistent with abiotic oxidation by O2. The oxidation of Fe(II) to form primary Fe(III) phases contributed to banded iron-formations (BIFs) during the Precambrian. Both oxygenic photosynthesis, which produces O2 as an oxidizing waste product, and anoxygenic photosynthesis in which Fe(II) is used to fix CO2 have been proposed as Fe(II) oxidation mechanisms. Although we do not know the specific mechanisms responsible for all Precambrian Fe(II) oxidation, we assessed the relative importance of both mechanisms in this modern hot spring environment. In this environment, cyanobacterial oxygen production accounted for all the observed Fe(II) oxidation. The rate data indicate that a modest population of cyanobacteria could have mediated sufficient Fe(II) oxidation for some BIFs.  相似文献   

19.
贵州云峰铝土矿中铀矿物的发现   总被引：1，自引：1，他引：0  
有关铝土矿中铀富集的报道很多,但至今未见独立铀矿物存在的相关文献。本次研究采用岩相学观察、X衍射(XRD)、ICP-MS、电子探针(EPMA)、拉曼光谱分析等手段,对黔中典型的铝土矿——云峰铝土矿中的晶质铀矿进行了研究。研究发现该铝土矿床中,铀富集明显(w(U)(18×10~(-6)～62×10~(-6)),平均值35×10~(-6)),铀矿物大小呈微米至亚微米级,围绕锐钛矿边缘生长、或充填于高岭石微裂隙中、或散布于与黄铁矿密切相关的高岭石或硬水铝石中。铀矿物的主要组分为UO_2(w(UO_2)为52.2%～80.88%)和TiO_2(w(TiO_2)为1.85%～14.98%);电子探针面扫描显示铀矿物中钛分布不均匀;铀矿物的拉曼特征波长为442 cm~(-1)和454 cm~(-1),因此,初步推测铀矿物为晶质铀矿和含钛晶质铀矿。其形成过程大致如下,来源于下寒武统牛蹄塘组黑色岩系中的铀(U~(4+))在风化过程中氧化为U~(6+)、析出、被Al~-, Fe~-氧化物/氢氧化物吸附;在沉积和成岩过程中,随着三水铝石转变为勃姆石和硬水铝石、铁氧化/氢氧化物转变为黄铁矿,吸附的铀解吸、还原(U~(6+)至U~(4+))、最后形成铀矿物。  相似文献   

20.
In this study, the valence states of uranium in synthetic and natural brannerite samples were studied using a combination of transmission electron microscopy-electron energy loss spectroscopy, scanning electron microscopy-energy dispersive X-ray analysis (SEM-EDX), and X-ray photoelectron spectroscopy (XPS) techniques. We used a set of five (UO2, CaUO4, SrCa2UO6, UTi2O6, and Y0.5U0.5Ti2O6) U standard samples, including two synthetic brannerites, to calibrate the EELS branching ratio, M5/(M4 +M5), against the number of f electrons. The EELS data were collected at liquid nitrogen temperature in order to minimise the effects of electron beam reduction of U6+ and U5+. Test samples consisted of three additional synthetic brannerites (Th0.7U0.3Ti2O6, Ca0.2U0.8Ti2O6, and Th0.55U0.3Ca0.15Ti2O6) and three natural brannerites from different localities. The natural brannerite samples are all completely amorphous, due to cumulative alpha decay events over geological time periods (24–508 Ma). Our U valence calibration results are in reasonable agreement with previous work, suggesting possibly a non-linear relationship between the branching ratio and the number of f electrons (and hence the average valence state) of U in solids. We found excellent agreement between the nominal valence states of U and the average valence states determined directly by EELS and estimated by EDX analysis (with assumptions regarding stoichiometry) in two of the three synthetic brannerite test samples. The average U oxidation states of the five synthetic brannerite samples, as derived from XPS analyses, are also in good agreement with those determined by other techniques. The average valence states of U in three amorphous (metamict) natural brannerite samples with alpha decay doses ranging from 3.6×1016 to 6.9×1017 /mg were found to be 4.4, 4.7, and 4.8, consistent with the presence of U5+ and/or U6+ as well as U4+ in these samples. These results are in general agreement with previous wet chemical analyses of natural brannerite. However, the average valence states inferred by SEM-EDX for two of the natural brannerite samples do not show satisfactory agreement with the EELS determined valence. This may be due to the occurrence of OH– groups, cation vacancies, anion vacancies, or excess oxygen in the radiation-damaged structure of natural brannerite.  相似文献   

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