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本文报道的纤碳铀矿产于湖南某花岗岩型铀矿床氧化带中。纤碳铀矿是一种铀酰碳酸盐矿物,在中国是首次发现。本文作了系统的矿物研究并与国外资料作了对比。 相似文献
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本文分析了广西花山铀矿床氧化带中铀酰矿物的类型、组合及赋存特征,探讨铀酰矿物的成因机制及其对深部铀矿体勘查的指示意义。研究发现,花山铀矿床氧化带中铀酰矿物的类型非常复杂,长冲、白石脚和糙米坪等三个矿点出现不同的铀酰矿物组合。长冲矿点发育准钙铀云母、钙铀云母和硅钙铀矿等铀酰磷酸盐和铀酰硅酸盐组合,铀酰矿物的阳离子组分以富Ca为特点;白石脚矿点出现硅铅铀矿和斜磷铅铀矿等铀酰硅酸盐组合,铀酰矿物的阳离子组分以富Pb为特点;糙米坪矿点出现翠砷铜铀矿、铜铀云母和脂状铅铀矿等铀酰磷酸盐、铀酰砷酸盐和铀酰氢氧化物组合,铀酰矿物的阳离子组分以富Cu和As等为特点。花山铀矿床中的铀酰矿物是原生铀矿物(推断为沥青铀矿)在氧化环境下发生次生沉淀作用而形成的,三个矿点铀酰矿物组合的差异归因于原生铀矿体元素地球化场、地下水中络阴离子类型和地下水介质pH环境等多种因素的耦合。研究认为,铀矿床氧化带中的铀酰矿物对于指导深部盲矿勘查具有一定的指示意义。在花山地区,铀酰矿物沿断裂带出现大规模的垂向分布,它的发育位置大致记录了原生铀矿体的产状特征,而铀酰矿物的含量和类型则有助于提供原生铀矿石品位和硫化物含量等重要的成矿信息。本研究预测,在花山矿区内的糙米坪和白石脚矿点仍然存在发现氧化型铀矿体的良好潜力。 相似文献
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下庄铀矿为一花岗岩型铀矿，矿田地处湿热气候条件下，沥青铀矿普遍产于破碎带中，这种特定的产出环境致使该区沥青铀矿经受了强烈的风化，形成种类繁多、数量丰富的铀酰矿物；而我国高放废物地质处置库拟建在花岗岩体中。因此，下庄铀矿田是开展核废料氧化的天然类比研究的理想地区，并对我国的高放废物地质处置库的安全性评价有重要的指导作用。下庄铀矿田的铀酰矿物组合为铀酰氢氧化物、铀酰硅酸盐和铀酰磷酸盐，包括柱铀矿、黄钙铀矿、calciouranoite、红铀矿、富硅铀酰相、硅钙铀矿、钙铀云母和盈江铀矿等。根据它们的空间分布特征可划分成两个风化系列，即硅酸盐风化系列和磷酸盐风化系列，其共生次序分别为：沥青铀矿→铀酰氢氧化物（氧化物）→富硅铀酰相→硅钙铀矿和沥青铀矿→铀酰氢氧化物（氧化物）→钙铀云母→盈江铀矿。在该矿田中，铀酰氢氧化物是亚稳定相矿物，常常被铀酰硅酸盐或磷酸盐取代，因此，铀酰氢氧化物仅出现在少数样品中，而铀酰硅酸盐和铀酰磷酸盐矿物则非常普遍。矿田中的铀酰矿物在化学成分上以富钙为其显著特征，由于核废料地质处置库近场地下水中的Ca^2＋含量应该明显比下庄矿田地下水中的高，因此，我们预测含Ca的铀酰硅酸盐和铀酰磷酸盐矿物等热力学上的稳定物相很可能是地质处置系统中最主要的铀酰矿物，处置库内放射性核素的迁移主要是由这些矿物控制的。 相似文献
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Sorption interactions with montmorillonite and other clay minerals in soils, sediments, and rocks are potentially important mechanisms for attenuating the mobility of U(6+) and other radionuclides through the subsurface environment. Batch experiments were conducted (in equilibrium with atmospheric % MathType!MTEF!2!1!+-% feaafeart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXafv3ySLgzGmvETj2BSbqefm0B1jxALjhiov2D% aebbfv3ySLgzGueE0jxyaibaiiYdd9qrFfea0dXdf9vqai-hEir8Ve% ea0de9qq-hbrpepeea0db9q8as0-LqLs-Jirpepeea0-as0Fb9pgea% 0lrP0xe9Fve9Fve9qapdbaqaaeGacaGaaiaabeqaamaabaabcaGcba% acbiGaiWiG-bfadaWgaaWcbaacbaGaa43qaiaa+9eadaWgaaqaaiaa% +jdaaWqabaaaleqaaaaa!400D!\[P_{CO_2 } \])to determine the effects of varying pH (2 to 9), solid-mass to solution-volume ratio (M/V = 0.028 to 3.2 g/L), and solution concentration (2 × 10–7 and 2 × 10–6 M 233U) on U(6+) sorption on SAz-1 montmorillonite. The study focused on U(6+) surface complexation on hydroxylated edge sites as the sorption mechanism of interest because it is expected to be the predominant sorption mechanism at pHs typical of natural waters (pH 6 to 9). Thus, the experiments were conducted with a 0.1 M NaNO3 matrix to suppress ion-exchange between U(6+) in solution and interlayer cations. The results show that U(6+) sorption on montmorillonite is a strong function of pH, reaching a maximum at near-neutral pH (6 to 6.5) and decreasing sharply towards more acidic or more alkaline conditions. A comparison of the pH-dependence of U(6+) sorption with that of U(6+) aqueous speciation indicates a close correspondence between U(6+) sorption and the predominance field of U(6+)-hydroxy complexes. At high pH, sorption is inhibited due to formation of aqueous U(6+)-carbonate complexes. At low pH, the low sorption values indicate that the 0.1 M NaNO3 matrix was effective in suppressing ion-exchange between the uranyl (UO2
2+) species and interlayer cations in montmorillonite. At pH and carbonate concentrations typical of natural waters, sorption of U(6+) on montmorillonite can vary by four orders of magnitude and can become negligible at high pH.The experimental results were used to develop a thermodynamic model based on a surface complexation approach to permit predictions of U(6+) sorption at differing physicochemical conditions. A Diffuse-Layer model (DLM) assuming aluminol (>AlOH) and silanol (>SiOH) edge sites and two U(6+) surface complexation reactions per site effectively simulates the complex sorption behavior observed in the U(6+)-H2O-CO2-montmorillonite system at an ionic strength of 0.1 M and pH > 3.5. A comparison of model predictions with data from this study and from published literature shows good agreement and suggests that surface complexation models based on parameters derived from a limited set of data could be useful in extrapolating radionuclide sorption over a range of geochemical conditions. Such an approach could be used to support transport modeling by providing a better alternative to the use of constant K
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s in transport calculations. 相似文献
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尤碳钙铀矿是一种含钙的铀酰碳酸盐矿物,在我国湖南省首次发现。它产于湖南某花岗岩型热液铀矿床氧化带中,与红铀矿、橙黄铀矿、水丝铀矿、β-硅钙铀矿、纤碳铀矿等共生。矿物为黄色。比重D_(?)=4.0,D_(cal)=4.16。在长波紫外线照射下发污黄绿色弱荧光。二轴晶,负光性。折光率α=1.635,β=1.626,γ=1.505,2V=40°±。斜方晶系。X射线粉晶分析主要强线为8.10(9),7.20(10),3.51(8),3.15(9)。微量化学全分析结果CaO 4.08%,UO_3 74.44%,CO_2 4.29%,H_2O 13.27%。化学式为Ca (UO_2)_3[CO_3](OH)_6·5H_2O。 相似文献
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硅钾铀矿属罕见的次生铀矿物,1986年我国首次发现于甘肃龙首山铀矿床氧化。带。对该矿物进行了多种测试工作。矿物为层状结构的铀酰硅酸盐矿物。晶胞参数a=6.62,b=7.03,c=7.06,β=105.2°。化学式:(K_(0·58) Na_(0·33)0.91(H_3O)[UO_2SiO_4]·0.8H_2O 相似文献
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