酸溶-电感耦合等离子发射光谱法测定密西西比型铅锌矿床矿石中的铅

密西西比型(MVT)铅锌矿床的主要矿物有方铅石、闪锌矿,常伴生有重晶石、萤石等矿物,使得MVT型矿石在酸处理过程中易生成不溶于水和酸的硫酸铅钡复盐,故而检测矿样中铅的含量偏低。本文建立了采用盐酸-硝酸-氢氟酸体系酸溶分解MVT型矿石,电感耦合等离子体发射光谱法(ICP-OES)测定铅含量的分析方法。实验比较了盐酸-硝酸-氢氟酸、盐酸-硝酸-氢氟酸-高氯酸、盐酸-硝酸-硫酸三种酸溶体系的溶样效果,并通过X射线衍射论证了方法的可行性。结果表明,盐酸-硝酸-氢氟酸体系克服了复盐硫酸铅钡和硫酸铅沉淀的生成,适量的氢氟酸促进了Pb SO4的溶解,X射线衍射表征也表明此种酸溶体系的沉淀中不含有Pb SO4,可更彻底地分解MVT型矿石。本方法精密度(RSD)为0.3%~0.6%,实际样品的加标回收率为96.0%~99.2%,铅的最佳检测范围为0.01%~20.0%。     

砂质碎屑储层钙质夹层形成机理及其主控因素分析

砂岩储层中局部钙的富集是影响储层物性的重要因素之一,因此揭示钙形成的主控因素及形成机理,对油田后期的高效开发无疑具有重要意义。在砂质碎屑岩中,钙的富集一般以"钙尖"的形式产出,有顶底钙形式、也有团块状等等。本文通过物理化学分析手段,剖析钙离子的来源,钙离子富集条件及钙质沉淀机理及其主控因素。研究结果表明,钙离子主要在同生、表生与深埋成岩作用期析出,各类酸性水是其催化条件。在同生与表生作用期,在湖(海)平面下降,河道变迁等条件下,通过蒸发作用,化学反应平衡左移,形成含钙化合物沉淀。利用苏里格气田东区目的层丰富的地下水地球化学组成分析资料,经综分析表明,目的层钙质夹层形成地质条件复杂,为深埋成岩、同生与表生混合作用下的产物,其中深埋成岩作是其主要形成时期,而其余少量钙质夹层则是在同生或表生期形成,并进一步明确了深埋成岩作用是苏里格气田东区钙质夹层富集的主控因素。     

硫代硫酸钠沉淀法富集铜冶炼废酸中铼的实验研究

白银有色集团铜业公司冶炼废酸量每年约为1×105m3,其中铼含量为5~70 mg/L,为综合利用废酸中的铼,采用硫代硫酸钠作为特效沉淀剂,对该沉淀剂加入量、反应时间、反应温度以及废酸中铼含量对铼沉淀率的影响做了较系统的实验研究,得到较优化的沉淀条件。进一步的中试放大实验取得了良好的技术指标:富铼渣泥中含铼达1.66%,铼的回收率达到99.8%。在此基础上,对沉淀剂的氧化还原反应机理进行了探讨。本方法工艺简单,铼沉淀率高,环境友好,较适用于废酸中铼的高效提取。     

钻井液类型对南极冰层取心钻进工作的影响

钻井液的类型与性能对于提高极地冰层取心钻进的效率与保证钻孔稳定性具有重要的影响。在分析铠装电动机械钻具工作原理与钻井液循环方式的基础上,较为详细地分析了升降钻具的速度与钻井液粘度与密度之间的关系;分析了现有钻井液类型和所存在的问题;以二元脂肪酸二醇酯、低分子量饱和脂肪酸酯与甲基硅油的试验测试数据为基础,确定了可用于极地冰层取心钻进的钻井液类型及其性能要求。     

大兴安岭中北段塔尔气地区早白垩世白音高老组火山岩地球化学特征及意义

塔尔气地区早白垩世白音高老组火山岩主要由流纹岩、流纹质(含角砾)岩屑晶屑凝灰岩及流纹质岩屑晶屑凝灰熔岩等组成。岩石地球化学研究表明,火山岩具有富铝(Al2O3含量13.37%~15.79%)、富碱(Na2O+K2O含量6.10%~8.56%)、贫镁钙的特点;稀土元素丰度总量较高,轻、重稀土元素分馏明显[(La/Yb)N=3.72~17.9],且HREE有较明显的凹陷;微量元素以相对富集K、Rb、Ba、LREE等大离子亲石元素,而相对亏损Sr元素以及高场强元素Nb、Ta、Ti为特征。结合前人研究结果表明,塔尔气地区白音高老组火山岩来源于基性下地壳物质的部分熔融。结合火山岩所具有的A型流纹岩的特点,暗示为伸展构造体制下的产物,可能与蒙古—鄂霍茨克洋闭合后的伸展环境有关。     

Characterization of low-molecular-weight organic acids isolated from the Toarcian argillite pore water (Tournemire site,France)

Bacterial activity in the near-field environment of radioactive waste disposal facilities in deep argillaceous rocks is currently under investigation. Bacterial development could be enhanced by the availability of low-molecular-weight organic acids (LMWOA) dissolved in the pore water of clayey rocks. This study firstly aimed at isolating and characterizing the LMWOA of the Toarcian argillite from the Tournemire Underground Research Laboratory (France, Aveyron). It also aimed at assessing the disturbing effects that could be induced by a disposal facility on the type and release of LMWOA (exposure to oxygen, alkaline pH, temperature increase). Under the experimental conditions investigated at 60 °C, the mean dissolved organic carbon (DOC) is about 15 mg L⁻¹ with a LMWOA proportion of 35 %. The main LMWOA are composed of formate, fumarate, propionate, acetate, and lactate. DOC is mainly influenced by both temperature and pH increases, whereas the LMWOA type nature and release are more specifically affected by the exposure to oxygen.     

Mass Fractions of S,Cu, Se,Mo, Ag,Cd, In,Te, Ba,Sm, W,Tl and Bi in Geological Reference Materials and Selected Carbonaceous Chondrites Determined by Isotope Dilution ICP‐MS

Mass fractions of S, Cu, Se, Mo, Ag, Cd, In, Te, Ba, Sm, W and Tl were determined by isotope dilution sector field ICP‐MS in the same sample aliquot of reference materials using HF‐HNO₃ digestion in PFA beakers in pressure bombs and glassy carbon vessels in a high‐pressure asher (HPA‐S) for comparison. Additionally, Bi was determined by internal standardisation relative to Tl. Because isobaric and oxide interferences pose problems for many of these elements, efficient chromatographic separation methods in combination with an Aridus desolvator were employed to minimise interference effects. Repeated digestion and measurement of geological reference materials (BHVO‐1, BHVO‐2, SCo‐1, MAG‐1, MRG‐1 and UB‐N) gave results with < 5% relative intermediate precision (1s) for most elements, except Bi. Replicates of NIST SRM 612 glass digested on a hot plate were analysed by the same methods, and the results agree with reference values mostly within 2% relative deviation. Data for the carbonaceous chondrites Allende, Murchison, Orgueil and Ivuna are also reported. Digestion in a HPA‐S was as efficient as in pressure bombs, but some elements displayed higher blank levels following HPA‐S treatment. Pressure bomb digestion yielded precise data for volatile S, Se and Te, but may result in high blanks for W.     

Response of surface water chemistry to reduced levels of acid precipitation: comparison of trends in two regions of New York,USA

In light of recent reductions in sulphur (S) and nitrogen (N) emissions mandated by Title IV of the Clean Air Act Amendments of 1990, temporal trends and trend coherence in precipitation (1984–2001 and 1992–2001) and surface water chemistry (1992–2001) were determined in two of the most acid‐sensitive regions of North America, i.e. the Catskill and Adirondack Mountains of New York. Precipitation chemistry data from six sites located near these regions showed decreasing sulphate (SO₄^2?), nitrate (NO₃^?), and base cation (C_B) concentrations and increasing pH during 1984–2001, but few significant trends during 1992–2001. Data from five Catskill streams and 12 Adirondack lakes showed decreasing trends in SO₄^2? concentrations at all sites, and decreasing trends in NO₃^?, C_B, and H⁺ concentrations and increasing trends in dissolved organic carbon at most sites. In contrast, acid‐neutralizing capacity (ANC) increased significantly at only about half the Adirondack lakes and in one of the Catskill streams. Flow correction prior to trend analysis did not change any trend directions and had little effect on SO₄^2? trends, but it caused several significant non‐flow‐corrected trends in NO₃^? and ANC to become non‐significant, suggesting that trend results for flow‐sensitive constituents are affected by flow‐related climate variation. SO₄^2? concentrations showed high temporal coherence in precipitation, surface waters, and in precipitation–surface water comparisons, reflecting a strong link between S emissions, precipitation SO₄^2? concentrations, and the processes that affect S cycling within these regions. NO₃^? and H⁺ concentrations and ANC generally showed weak coherence, especially in surface waters and in precipitation–surface water comparisons, indicating that variation in local‐scale processes driven by factors such as climate are affecting trends in acid–base chemistry in these two regions. Copyright © 2005 John Wiley & Sons, Ltd.     

Temporal and spatial variability of cation and silica export in an alpine watershed,Emerald Lake,California

A reaction set of possible mineral weathering reactions is proposed to explain observed cation and silica export for the Emerald Lake watershed, a small Sierra Nevada, California catchment. The reaction set was calculated through a stoichiometric mole‐balance method, using a multiyear record of stream flow and snowpack chemical analyses and site‐specific mineral compositions. Reaction‐set calculations were intended to explore how the processes controlling stream cation and silica export depend on differing bedrock mineralogy across the catchment as snowmelt and runoff patterns change over the year. Different regions within the watershed can be differentiated by lake inflow subdrainages, each exhibiting different stream‐flow chemistry and calculated weathering stoichiometry, indicating that different silica and cation generation processes are dominant in wet steep portions of the catchment. Short‐term differences in stream concentrations were assumed to reflect ion exchange equilibria and rapid biological processes, whereas long‐term persistent stream concentration differences in different areas of the catchment were assumed to reflect spatial variability in mineral weathering stoichiometry. Mineralogical analyses of rock samples from the watershed provided site‐specific chemical compositions of major mineral species for reaction calculations. Reaction sets were evaluated by linear regression of calculated versus observed differences between snowmelt and stream‐flow chemistry and by a combined measure. Initially, single weathering reactions were balanced and evaluated to determine the reactions that best explained observed stream chemical export. Next, reactions were combined, using mineral compositions from different rock types to estimate the dependence of ion fluxes on lithology. The seasonal variability of major solute calculated fluxes is low, approximately one order of magnitude, relative to the observed three orders of magnitude variability in basin discharge. Reaction sets using basin‐averaged lithology and Aplite lithologies gave superior explanations of stream chemical composition. Copyright © 2004 John Wiley & Sons, Ltd.     

柠檬酸发酵中的限制性因子

回顾柠檬酸发酵生化机制的发展历史，综合多年来的研究成果和结合生产实践中出现的问题，推断最有可能的柠檬酸发酵途径。影响柠檬酸发酵的限制性因子有Ｆｅ２＋、Ｍｎ２＋、Ｍｇ２＋、Ｋ＋、Ｐｉ、ＡＤＰ、ＡＴＰ、ＧＴＰ、ＣＯ２等，它们分别作用于发酵的关键酶顺乌头酸酶、丙酮酸羧化酶、柠檬酸合成酶、丙酮酸激酶等。生产实践中应该根据不同菌株而选择控制Ｆｅ２＋、Ｍｇ２＋、Ｍｎ２＋，Ｋ＋等金属离子。