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花岗岩型碳酸钠质交代热液铀矿床蚀变带中的重矿物有明显的改造与叠加现象。随着矿物的解离,热液从围岩中获取了部分矿源。主要铀矿化是在热液连续活动的晚期,铀与金属硫化物共沉淀。本文就西北某花岗岩体在碳酸钠质热液作用下所发生的重矿物组合含量及主要重矿物性质的一系列变化,以及与此有关的铀的活化转移与沉淀阶段等问题进行讨论。 相似文献
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以无水乙醇为溶剂、1-丁基-3-甲基咪唑四氟硼酸盐([Bmim]BF4)离子液体为表面活性剂,以钛酸四丁酯、六水合硝酸镧为原料,采用共沉淀法制备了不同掺镧量的La-TiO2光催化材料。采用X-射线衍射仪(XRD)、傅里叶变换红外光谱仪(FTIR)、场发射扫描电镜(FESEM)、差热-热重分析仪(TG-DSC)、紫外-可见吸收光谱仪(UV-vis)、比表面及孔隙度分析仪(BET)对其结构、形貌、热稳定性、光学性能及比表面积进行表征。所制备产品的光催化性能在紫外光下进行了光催化降解甲基橙实验,实验结果表明在离子液体的量为0.5mL,掺杂镧量为5%的TiO2纳米材料对甲基橙的降解效果相对较好,降解率最高达到98.73%。 相似文献
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In natural waters arsenic normally occurs in the oxidation states +III (arsenite) and +V (arsenate). The removal of As(III) is more difficult than the removal of As(V). Therefore, As(III) has to be oxidized to As(V) prior to its removal. The oxidation in the presence of air or pure oxygen is slow. The oxidation rate can be increased by ozone, chlorine, hypochlorite, chlorine dioxide, or H2O2. The oxidation of As(III) is also possible in the presence of manganese oxide coated sands or by advanced oxidation processes. Arsenic can be removed from waters by coprecipitation with Fe(OH)3, MnO2 or during water softening. Fixed‐bed filters have successfully been applied for the removal of arsenic.The effectiveness of arsenic removal was tested in the presence of adsorbents such as FeOOH, activated alumina, ferruginous manganese ore, granular activated carbon, or natural zeolites. Other removal technologies are anion exchange, electrocoagulation, and membrane filtration by ultrafiltration, nanofiltration or reverse osmosis. 相似文献
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Duygu Ozdes Celal Duran Hacer Bayrak Volkan Numan Bulut Mehmet Tufekcı 《洁净——土壤、空气、水》2012,40(2):211-217
A new separation and preconcentration technique based on coprecipitation of Cu(II) and Ni(II) ions by the aid of Mo(VI)/di‐tert‐butyl{methylenebis[5‐(chlorobenzyl)‐4H‐1,2,4‐triazol‐3,4‐diyl]}biscarbamate (BUMECTAC) precipitate has been established. The Mo(VI)/BUMECTAC precipitate was dissolved by concentrated HNO3 and the solution was completed to 5.0 mL with distilled/deionized water. The levels of the analyte ions were determined by flame atomic absorption spectrometer. The effects of experimental conditions like HNO3 concentration, amount of BUMECTAC and Mo(VI), sample volume, etc. and also the influences of some foreign ions were investigated in detail on the quantitative recoveries of analyte ions. The preconcentration factors were found to be 40 for Cu(II) and 100 for Ni(II) ions. The detection limits for Cu(II) and Ni(II) ions based on 3σ (N:10) were 0.43 and 0.70 µg L?1, respectively. The relative standard deviations were found to be lower than 4.0% for both analyte ions. The accuracy of the method was checked by spiked/recovery tests and the analysis of two certified reference materials (Environment Canada TM‐25.3 and CRM‐SA‐C Sandy Soil C). The procedure was successfully applied to sea water and stream water as liquid samples and baby food as solid sample in order to determine the levels of Cu(II) and Ni(II) ions. 相似文献
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Iron oxyhydroxide precipitates associated with acid mine drainage (AMD) from the Stearns Coal Zone in southeastern Kentucky
were analyzed for their metal (Al, Cu, Pb, Mn, Ni, and Zn) content. The most concentrated metals within these sediments are
nickel (27–32×103μmol/kg), manganese (16–29×103μmol/kg), and aluminum (13–22×103μmol/kg) as determined by HCl-HNO3 digestion. Metal concentrations associated with the organic fraction as determined by H2O2 digestion were generally far lower, with the exception of aluminum. "Batch" experiments (at initial pH=2.0) were used to
analyze the stability of these metals associated with a contaminated soil. Aluminum was the most mobile of the metals, presumably
the result of the formation of aluminum-sulfate aqueous complexes. The solubilization rates for nickel and iron were very
similar, suggesting that nickel, unlike the other metals, coprecipitated with iron in these sulfatic oxyhydroxides.
Received: 9 October 1997 · Accepted: 15 December 1997 相似文献
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Application of a coprecipitation method combined with low-background γ-spectrometry allowed the isolation of 7Be, 137Cs, 210Pb, and radium and thorium isotopes together with BaSO4, Fe(OH)3, or AMP/Cs in 18 L of coastal water. This simple method showed high chemical yields of 77–91% (mean, 85%) for 210Pb and radium isotopes, 87–92% (mean, 91%) for 7Be and thorium isotopes, and 98% for 137Cs. The activity of the nuclides showed good reproducibility with standard deviations of 1–8%, while the deviation of activity
in particle-reactive 210Pb (32%) and 7Be (21%) in filtered water samples was exceptionally large. 相似文献
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The coprecipitation method is widely used for the preconcentration of trace metal ions prior to their determination by flame atomic absorption spectrometry (FAAS). A simple and sensitive method based on coprecipitation of Fe(III) and Ni(II) ions with Cu(II)‐4‐(2‐pyridylazo)‐resorcinol was developed. The analytical parameters including pH, amount of copper (II), amount of reagent, sample volume, etc., were examined. It was found that the metal ions studied were quantitatively coprecipitated in the pH range of 5.0–6.5. The detection limits (DL) (n = 10, 3s/b) were found to be 0.68 µg L?1 for Fe(III) and 0.43 µg L?1 for Ni(II) and the relative standard deviations (RSD) were ≤4.0%. The proposed method was validated by the analysis of three certified reference materials (TMDA 54.4 fortified lake water, SRM 1568a rice flour, and GBW07605 tea) and recovery tests. The method was successfully applied to sea water, lake water, and various food samples. 相似文献
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《Chemie der Erde / Geochemistry》2016,76(1):133-148
The variation of major and rare earth elements and yttrium (REY) in the monomictic hardwater Lake Tiberias during the wet and dry seasons of the hydrological year was studied in two profiles. The average volume and Cl concentration of the known and unknown saline inflows of 1.6 × 107 m3 and 1.2 × 109 mol are derived by closing both balances. This brine corresponds to a mixture of 83% of groundwater from Cretaceous aquifers and 17% of very saline deep brine. Taking cycling of calcite in the hypolimnion into account, the settling rate of authigenic calcite is estimated to be 3.3 mol m−2 a−1.In the stratified lake of the dry season dissolved inorganic carbon increases by 490 μM at the thermo-/chemocline due to microbial reduction of SO42−, NO3−, chemical reduction of Fe(III) and MnO2 colloids, and cycling of calcite in the hypolimnion. REY distribution in the stratified water column is dominantly controlled by coprecipitation with calcite, hydrous ferric oxides and MnO2 in the epilimnion and cycling of these compounds in the hypolimnion. The positive Ce anomaly in the hypolimnetic water is produced by cycling of MnO2. The simulation of the increase of REY in the hypolimnion reveals that hydrous ferric and manganese oxides only play a negligible role except Ce. Only about 10% of REY from cycled matter enhance REY in solution. Most of the released REY are adsorbed by particular matter and thus settling on the floor of the lake.Different from Na, U, SO42− and SiO2, the other elements, in particular REY, increase in the mixed water column from the top to the lower third and mostly decrease thereafter toward the bottom in the mixed lake during the wet season. The behavior of REY is caused by some cycling of calcite and pH-dependent re-equilibration of REY bound to hydrous ferric and manganese oxides adsorbed by particular matter. 相似文献
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I. de Vicente K. Cattaneo L. Cruz-Pizarro A. Brauer P. Guilizzoni 《Journal of Paleolimnology》2006,35(1):55-64
P-fractional composition has been studied in a 64-cm long sediment core collected in an eutrophic hardwater lake (Lake Alserio,
northern Italy) in an attempt to identify the main mechanisms (chemical or biologic) controlling CaCO3 precipitation in the water column. The results of the sedimentary phosphate fractionation showed that the most important
P fraction was an organic fraction extracted with hot NaOH: org-Palkali (26% of Psed). A digestion of the supernatant of the P-fraction bound to CaCO3 allowed the detection of a large pool of org-P (19% of Psed). Although the nature of this fraction is unclear, we suggest that it may be involved in the biologically mediated precipitation
of CaCO3. The high CaCO3 concentration in the entire vertical sediment profile, as well as the presence of inorg- and org-P bound to Ca in both laminated
and non-laminated zones, suggest that the CaCO3 precipitation is not a recent process but is a process that has been occurring in the lake for some time. Accordingly, the
change from a homogeneous sediment to a laminated sequence might be caused by the eutrophication process of Lake Alserio occurring
since the 1960s, which has allowed the preservation of the varved sediment as a consequence of the drastic reduction in bioturbation. 相似文献
10.
Natural analogue investigations aim to understand key phenomena and processes in natural systems related to those expected to occur in radioactive waste repositories. One of the key applications of natural analogue studies has been the possibility to test the geochemical models to be used to describe the migration of radionuclides in a future radioactive waste repository system. To this end, several geochemical modelling testing exercises (commonly denoted as blind predictive modelling, BPM) have formed an integral part of these studies over the last decade.
We have reviewed, discussed and compared the results obtained from geochemical modelling BPM exercises carried out within six natural analogue studies: Poços de Caldas, Cigar Lake, Maqarin, El Berrocal, Oklo and Palmottu. To make this comparison meaningful, we present the main geochemical characteristics of each site in order to highlight the most relevant mineralogical and hydrochemical differences. The elements selected for discussion are: Sr, Ba, Sn, Pb, Se, Ni, Zn, REEs, Th and U. We have based our discussion on the results obtained from the calculated aqueous speciation as well as by comparing solubility calculations with the actually observed concentrations.
Results can be differentiated into two categories of elemental behaviour:
1. those elements like Th and U under reducing conditions that can be fairly well described by assuming solubility control exerted by pure solid phases as their oxyhydroxides;
2. elements such as Sr, Zn, REEs and U under oxidising conditions for which the association to major geochemical components of the system must be considered in order to explain their concentrations in groundwaters.
Additionally, we discuss the main improvements made to the thermodynamic databases and the geochemical calculation methodologies due to the BPM exercises. Furthermore, the most important characterisation geochemical data needed to complete predictive solubility and speciation calculations are identified. 相似文献
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