α—巯基苯骈噻唑吸附光度法测定矿石中痕量金     

龚治湘  袁书荣 《铀矿地质》1992,8(1):52-56

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金在黄铁矿表面沉淀机理的实验研究   总被引：6，自引：0，他引：6       下载免费PDF全文

曾贻善  姜士军 《地质科学》1996,31(1):90-96

为了研究金在黄铁矿表面沉淀的机理,于室温、常压,在氯化物溶液中进行了黄铁矿粉末吸附金的实验。在不同pH的溶液中,黄铁矿均可吸附金,而且pH值明显地影响吸附速率。扫描电镜观察表明,反应后黄铁矿粒表面有金晶体形成。XPS研究得知,黄铁矿光片与含金氯化物溶液反应后表面有A⁰存在;硫在反应初期为S⁰、S₂O₃^2-,随后转变为SO₄^2-,而铁成为Fe³⁺.黄铁矿中的Fe²⁺和S₂^2-是溶液中金的还原剂。金在黄铁矿表面沉淀可能涉及吸附、还原和晶体生长等过程。  相似文献   

水合氧化锆吸附硼的研究     

张国防  孙国清 《海洋科学》1995,19(2):58-61

详细地研究了硼在水合氧化锆吸附剂上的吸附行为。研究结果表明，水合氧化锆的吸硼速率较快，２ｈ可完全达平衡，且吸附可用Ｆｒｅｕｎｄｌｉｃｈ等温吸附线很好地拟合。被吸附的硼易被碱液洗脱，通过水合氧化锆上硼的“吸附－脱附循环”研究，表明该吸附剂的吸附性能好，再生能力强，循环使用寿命长，是一种很有价值的高效脱硼吸附剂。  相似文献   

Uptake of platinum group elements by the marine macroalga, Ulva lactuca     

Andrew Turner  Marie S. Lewis  Leyla Shams  Murray T. Brown 《Marine Chemistry》2007,105(3-4):271-280

Uptake of environmentally relevant platinum group elements (PGE) by the marine macroalga, Ulva lactuca, has been studied. Removal of nM concentrations of Rh(III), Pd(II) and Pt(IV) added to filtered sea water appeared to proceed via pseudo-first-order kinetics, with respective forward rate constants of either 0.0039 or 0.0042 h^− 1, 0.0058 or 0.0096 h^− 1 and 0.0017 or 0.0032 h^− 1, depending on whether an irreversible or reversible reaction was invoked. The (quasi-) equilibrium distribution coefficients, derived from linear fits to uptake (sorption) isotherms, were about 1400, 900 and 350 mL g^− 1 on a dry mass basis for Rh, Pd and Pt, respectively. With increasing sea water pH, over the range 7.9 to 8.4, uptake of Rh by Ulva increased considerably, whereas a small increase in Pt removal was observed; in contrast, uptake of Pd exhibited no clear dependence on pH. The percentage of metal taken up that was internalised within cells, evaluated by washing selected algal samples in 3 mM EDTA, was about 40% for Rh, 80% for Pd and 95% for Pt. Results of this study were interpreted in terms of what is known about the aqueous speciation of PGE in sea water. Thus, Rh exists as cationic hydrated chloride complexes which are readily adsorbed at the algal surface. Palladium has an exceptional affinity for organic ligands, and uptake (and internalisation) appears to be governed by competition for Pd²⁺ from aqueous and algal binding sites. Platinum (IV) exists predominantly as a series of (mainly) negatively charged chloride and mixed hydroxychloride complexes that have little propensity to interact with the algal surface; however, its high degree of internalisation requires at least some interaction with specific and perhaps physiologically active sites.  相似文献   

Removal Performance of Tetracycline and Oxytetracycline From Aqueous Solution Via Natural Zeolites: An Equilibrium and Kinetic Study     

《洁净——土壤、空气、水》2017,45(10)

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砂岩含水介质中铀的吸附和迁移行为研究     

崔迪  杨冰  郭华明  连国玺  孙娟 《地学前缘》2022,29(3):217-226

地浸铀矿山退役后,含水层中残留的含铀浸出液随着地下水的运动向下游迁移扩散,存在对周边地下水污染的风险。本文设计了若干组批实验和柱实验,研究铀在北方某地浸铀矿山砂岩含水介质中的吸附和迁移行为。实验结果表明,砂岩对铀的吸附在12 h以内达到平衡,铀初始浓度越高,砂岩的铀吸附容量越大;砂岩对铀的吸附为吸热反应,温度升高有利于吸附反应的进行。溶液pH值和共存 {\mathrm{HCO}}_3^{-}浓度会对铀的吸附作用产生强烈的影响:pH值在7左右时,铀的吸附量最高; {\mathrm{HCO}}_3^{-}浓度越高,铀的吸附量越低。这些影响是通过改变溶液中铀的络合形态和砂岩矿物表面的电荷性质实现的。柱实验表明,pH值、铀浓度、流速和 {\mathrm{HCO}}_3^{-}浓度是影响铀在饱和砂岩含水介质中迁移的重要因素。pH值≤7时,pH值越高,砂岩柱越不易被铀穿透;而铀浓度、流速、 {\mathrm{HCO}}_3^{-}浓度越高,砂岩柱越易被铀穿透。两点非平衡模型可以很好地拟合不同条件下铀在砂岩柱中的迁移过程。批实验获得的分配系数是柱实验的1.16.6倍。通过对比实验条件、含水层特性和地下水化学特征,确定分配系数为48.1 mL/g时,较适合描述研究区内砂岩含水层中的铀迁移。上述认识为地浸铀矿山地下水铀的反应运移过程和天然自净化机理提供了理论依据。  相似文献   

Effects of composition and pore structure on the reservoir gas capacity of Carboniferous shale from Qaidam Basin,China     

《Marine and Petroleum Geology》2015

Shale adsorption and breakthrough pressure are important indicators of shale gas development and key factors in evaluating the reservoir capacities of shales. In this study, geochemical tests, pore-structure tests, methane adsorption tests, and breakthrough-pressure tests were conducted on shales from the Carboniferous Hurleg Formation in eastern Qaidam Basin. The effects of the shale compositions and pore structures on the adsorption and breakthrough pressures were studied, and the reservoir capacities of the shales were evaluated by analyzing the shale adsorptions and sealing effects. The results indicate that the organic carbon content was only one of factors in affecting the adsorption capacity of the shale samples while the effect of the clay minerals was limited. Based on the positive correlation between the adsorption capacity and specific surface area of the shale, the specific surface area of the micropores can be used as an indicator to determine the adsorption capacity of shale. The micro-fracturing of brittle minerals, such as quartz, create a primary path for shale gas breakthrough, whereas the expansion of clay minerals with water greatly increases the breakthrough pressure in the shale samples. Methane adsorption tests showed that maximum methane adsorption for shale samples Z045 and S039 WAS 0.107 and 0.09655 mmol/g, respectively. The breakthrough pressure was 39.36 MPa for sample S039, maintained for 13 days throughout the experiment; however, no breakthrough was observed in sample Z045 when subjected to an injected pressure of 40 MPa for 26 days. This indicates that sample Z045, corresponding to a depth of 846.24 m, exhibited higher adsorption capacity and a better reservoir-sealing effect than sample S039 (498.4 m depth). This study provides useful information for future studies of Qaidam Basin shale gas exploration and development and for evaluation of shale quality.  相似文献   

Influence of hydrolysis on the sorption of metal cations by smectites: Importance of edge coordination reactions   总被引：1，自引：0，他引：1  

John M. Zachara  James P. McKinley 《Aquatic Sciences - Research Across Boundaries》1993,55(4):250-261

A comparison was made between the adsorptive behaviors of Cd²⁺ and UO ₂ ²⁺ relative to two smectites that differed in their ratio of edge sites to fixed-charge sites. Adsorption varied with both pH and ionic strength, consistent with sorptive contributions of ion exchange and coordination reactions to edge hydroxyls. Both clay minerals exhibited a greater affinity for UO ₂ ²⁺ than for Cd²⁺, and the clay with a higher proportion of edge sites retained both ions more strongly. A computational model including fixed-charge sites and edge hydroxyls resulted in a good prediction of overall UO ₂ ²⁺ and Cd²⁺ uptake to both smectites.  相似文献   

Analysis of the distribution coefficients and mobility characteristics of phenols in different soil types     

Zareen Khan  Y. Anjaneyulu 《Environmental Geology》2005,48(1):1-5

Adsorption studies were carried out on soil samples of high organic and low organic content to analyze the distribution coefficient and mobility of phenols. The results show that the amount of phenols adsorbed by the soil varies linearly with the fraction of organic carbon. Soils that are highly organic compared to those with low organic matter content retain the phenols to a greater extent. Adsorption studies on the different soil types indicated that the extent of adsorption of phenols by different kinds of soils is important, as a smaller amount of adsorption by the soil increases the risk of contamination of the groundwater supply.  相似文献   

Uranium and Thorium Isotope Distribution in an Offshore Bottom Sediment Core of the Selenga Delta, Lake Baikal, Siberia     

Aya Sakaguchi  Masayoshi Yamamoto  Keiichi Sasaki  Kenji Kashiwaya 《Journal of Paleolimnology》2006,35(4):807-818

Distribution of uranium and thorium isotopes in a short sediment core obtained offshore of the Selenga Delta in Lake Baikal, Siberia, was investigated to establish their sedimentary behaviors and to look for a linkage to paleoenvironmental changes. The sediments were composed of dominantly fine detrital materials (70–85%) and a relatively high sedimentation rate (ca. 0.03 cm y⁻¹). The depth profile of ²³⁸U content in bulk sediment samples showed a large variation of 70–123 Bq kg⁻¹, while ²³²Th profile showed a relatively narrow range from 36 to 56 Bq kg⁻¹. The observed ²³⁴U/²³⁸U activity ratios revealed a marked disequilibrium ranging from 1.53 to 1.84 with a mean value of 1.71 ± 0.07, demonstrating the presence of 50–80% authigenic ²³⁸U in the bulk sediments. The distribution of this authigenic ²³⁸U did not display any clear correlation with variations in sediment composition (organic, carbonate, Bio-SiO₂ and mineral contents) including grain size median. The profile of terrigenous ²³⁸U showed a relatively similar pattern to that of ²³²Th. Results of sequential leaching indicate that ²³⁸U in Fe–Mn oxyhydroxides fractions were responsible for the distribution of authigenic ²³⁸U rather than in Bio-SiO₂ fraction. The distribution of authigenic ²³⁸U in the bottom sediments may be explained by the fluctuation of U adsorption capacity on particles including organic matter and Fe–Mn oxyhydroxides before they entered the lake. This study highlights the potential use of authigenic and terrigenous U (Th) signatures in sediments to trace the behavior of U (Th) and to reconstruct environmental (e.g., hydrological) changes in the lake catchment area.  相似文献