广西荣华锰矿床地质特征及发现意义

广西荣华锰矿位于三叠系百逢组,在该地层中发现的工业锰矿床尚未见报道。通过对该矿区大比例尺地质填图,并结合地质工程和测试分析等手段,对矿床地质背景、沉积环境、矿体和矿石特征、沉积演化等进行分析研究,推测荣华锰矿为沉积-淋滤锰帽型矿床,矿体顺层分布于靠近罗楼组碳酸盐岩的百逢组第一段泥岩、泥质粉砂岩中,严格受地层和构造控制。矿石主要由偏锰酸矿、软锰矿等组成,矿石品位偏低,伴生Co等金属元素。百逢组之下的碳酸盐岩和百逢组第一段浊积砾岩层可作为该类锰矿上下界线典型的找矿标志。中三叠世桂西北处于盆包台构造格局,中晚古生代富含锰的台地在三叠纪遭受风化剥蚀,成矿元素被带入弧后盆地。随着特提斯洋闭合,挤压作用使盆地面积变小,水位加深,氧化还原界面波动,在百逢组第一段锰元素初步富集。后右江盆地抬升露出水面遭受剥蚀,风化淋滤作用最终形成该区顺层分布的氧化锰矿床。桂西广泛出露百逢组地层,其第一段具有良好的找矿前景。     

第一原理计算过渡金属掺杂尖晶石型LiMn2O4的电子结构

尽管对过渡金属掺杂锰酸锂后放电平台的升高现象有众多实验研究,但对其机理的研究却鲜见报道.采用第一原理的密度泛函理论,计算了过渡金属M(M=Ti、Cr、Fe、Co、Ni、Cu、Zn)掺杂尖晶石型LiMn2O4的电子结构,并以此分析放电平台的升高机理.电子态密度分析发现由于M-3d能带的诱导作用,出现了新的O-2p能带,而锂脱出时获得的电子,主要是由费米能级附近O-2p能带提供的.当过渡金属M由Ti变化到Zn时,M-3d能带逐渐向低能量的方向移动,新的O-2p能带出现的位置也随之下移,当Li脱出时,需要更多的能量才能从低能量的O-2p能带上获得电子,因而体系能够获得较高的嵌入电压.     

南海沉积物漫反射光谱反映的220ka以来东亚夏季风变迁

对南海越南岸外“太阳号”95航次17954孔220ka以来的沉积样品进行了漫反射光谱分析, 并从中提取F1和F2两个主因子及亮度和红度等漫反射光谱特征值, 发现漫反射光谱F1值和亮度反映了沉积物中的碳酸盐含量, 而漫反射光谱F2值和红度反映了沉积物中的铁氧化物含量, 后者可用作东亚夏季风的替代性指标.17954孔沉积物的漫反射光谱F2值显示, 倒数第二次冰消期东亚夏季风快速增长时间约在129ka; 本次工作还发现东亚夏季风在两次冰消期前的氧同位素2阶段和6阶段晚期各有一个异常强盛的时期.漫反射分析结果显示东亚夏季风主要受控于太阳辐射强度变化, 并明显地受低纬地区气候的影响.      

晚二叠世峨眉山地幔柱岩浆成矿作用

晚二叠世峨眉山地幔柱岩浆作用同时形成了Cu-Ni-PGE硫化物矿床和V-Ti-Fe氧化物矿床等不同类型的岩浆矿床。从硫化物矿床的PGE富集型、Cu-Ni-PGE富集型到Cu-Ni富集型,再到钒钛磁铁矿矿床,成矿基性-超基性岩体中基性岩石比例逐渐增加,PGE含量降低。铜镍铂族硫化物矿床具Nb和Ta负异常,岩浆流体组分含量较高,含有较高的H₂;而钒钛磁铁矿矿床具Nb、Ta和Ti正异常,Zr和Hf负异常,岩浆流体组分含量较低,含有较高的H₂O、CO₂和H₂。两类矿床强不相容元素和轻稀土元素(LREE)富集,Sr-Nd同位素组成与峨眉山玄武岩的演化趋势一致。Sr-Nd-Os-C-He同位素组成揭示岩浆上升过程中经历了不同程度的地壳混染,高钛玄武岩和钒钛磁铁矿矿床成矿岩体的地壳混染程度较低,部分低钛玄武岩和铜镍硫化物矿床存在明显的地壳混染。这两类岩浆矿床的形成与峨眉山地幔柱玄武岩浆有关,岩浆介质环境中H₂含量较高,V-Ti-Fe 氧化物矿床的形成与分离结晶、高含量的水和氧逸度的升高有关,Cu-Ni-(PGE)硫化物矿床的形成与还原性流体介质、结晶分异和地壳混染作用有关。     

滇东南中三叠统法郎组锰矿床成因的新认识

产于滇东南中三叠世拉丁期法郎组地层中的锰矿床,锰矿石出现氧化锰矿与碳酸盐锰矿混合存在现象,没有明显的变质现象,为沉积成因。矿石中一般都含有生物碎屑。我们对采自这一地区的斗南、岩子脚、老乌,土基冲等典型矿床的锰矿石样品,进行了系统的薄片显微镜和扫描电镜观察,同时应用X射线衍射对矿石矿物成份作了相应分析。观察到这些矿石中的鲕、豆状结构是由蓝绿藻类微生物凝聚作用形成的显微叠层构造,具有核形石特有的核心和包壳,其明—暗纹层相间的显微结构特征可以与现代深海大洋铁锰结核相类比。本文通过对核形石显微结构特征的观察和对锰矿物生成时介质环境的讨论,初步研究结果表明,锰矿形成可能位于古氧化还原界面附近,该区锰的富集可能与微生物活动密切相关。     

Manganese ore deposits in Koira-Noamundi province of Iron Ore Group, north Orissa, India: In the light of geochemical signature

Several small Mn–Fe oxide and Mn-oxide ore bodies associated with Precambrian Iron Ore Group of rocks are located within Koira-Noamundi province of north Orissa, India. These deposits are classified into in situ (stratiform), remobilized (stratabound) and reworked categories based on their field disposition. Volcaniclastic/terrigenous shale in large geographic extension is associated with these ore bodies.The in situ ore bodies are characterised by cryptomelane-, romanechite- and hematite-dominating minerals, low Mn/Fe ratio (1.1) and relatively lower abundance of trace (1500–2500 ppm) constituents. In such type of deposits the stratigraphic conformity of oxides with the tuffaceous shale suggests precipitation of Mn and Fe at a time of decreased volcaniclastic/terrigenous contribution. The minor and trace elements were removed from solution by adsorption rather than by precipitation. Both Mn and Fe oxides when precipitated adsorb trace elements strongly but the partitioning of elements takes place during diagenesis. The inter-elemental relationship reveals that Cu, Co, Ni, Pb and Zn were adsorbed on precipitating hydrous Mn oxides and form manganates. Some of these elements probably get desorbed from Fe oxide because of their inability to substitute for Fe³⁺ in the lattice of its oxide. However, P, V, As and Mo were less partitioned and retained in Fe-oxide phase. Positive correlation between Al₂O₃ and SiO₂, MgO, Na₂O, TiO₂ and some traces like Li, Nb, Sc, Y, Zr, Th and U points to their contribution through volcaniclastic/terrigenous detritus of both mafic and acidic composition.The remobilized ore bodies are developed in a later stage through dissolution, remobilization and reprecipitation of Mn oxides in favorable structural weak planes under supergene environment. Increase in average Mn/Fe ratio (8) and trace content (5000–8500 ppm) by 5–2.5 orders of magnitude, respectively, or more above its abundance in adjoining/underlying protore is characteristic of these deposits. The newly formed Mn ores constituting lithiophorite, cryptomelane/romanechite and goethite get quantitatively enriched in traces like Cu, Co, Ni, Pb and Zn. Positive correlation between Mn, Li, Co and Zn is due to the formation of mineral of lithiophorite–chalcophanite group during redistribution and reconcentration of Mn oxide. P and V, which were present in Fe oxide, also get dissolved and reprecipitate with Fe oxyhydroxide in these ores. Some other elements like Y, Th and U show positive relation with Fe. This is probably due to leaching of these elements during chemical weathering of associated shale and getting re-adsorbed in Fe-oxyhydroxide phase.However, under oxidizing environment selective cations like Ba, K, etc. resorb from Mn-structure, resulting in the development of pyrolusite (Mn/Fe>20). In such transformation, trace metals from pyrolusitic structure expels out, resulting thereby in a considerable reduction in total trace value (<3000 ppm).The reworked ore bodies are allochthonous in nature and developed through a number of stages during terrain evolution and lateritisation. Secondary processes such as reworking of pre-existing crust; solution and remobilization; precipitation and cementation and transport, etc. are responsible for their development. Such deposits are usually very low in Mn/Fe ratio (3) and trace content (<2000 ppm).     

Origin of Fe-Ti Oxide Ores in Mafic Intrusions: Evidence from the Panzhihua Intrusion, SW China

Economic concentrations of Fe–Ti oxides occur as massive,conformable lenses or layers in the lower part of the Panzhihuaintrusion, Emeishan Large Igneous Province, SW China. Mineralchemistry, textures and QUILF equilibria indicate that oxidesin rocks of the intrusion were subjected to extensive subsolidusre-equilibration and exsolution. The primary oxide, reconstructedfrom compositions of titanomagnetite in the ores and associatedintergrowths, is an aluminous titanomagnetite (Usp₄₀) with 40wt % FeO, 34 wt % Fe₂O₃, 16·5 wt % TiO₂, 5·3 wt% Al₂O₃, 3·5 wt % MgO and 0·5 wt % MnO. This compositionis similar to the bulk composition of the oxide ore, as inferredfrom whole-rock data. This similarity strongly suggests thatthe ores formed from accumulation of titanomagnetite crystals,not from immiscible oxide melt as proposed in earlier studies.The occurrence of oxide ores in the lower parts of the Panzhihuaintrusion is best explained by settling and sorting of densetitanomagnetite in the ferrogabbroic parental magma. This magmamust have crystallized Fe–Ti oxides relatively early andabundantly, and is likely to have been enriched in Fe and Tibut poor in SiO₂. These features are consistent with fractionationof mantle-derived melts under relatively high pressures (10kbar), followed by emplacement of the residual magma at 5 kbar.This study provides definitive field and geochemical evidencethat Fe–Ti oxide ores can form by accumulation in ferrogabbro.We suggest that many other massive Fe–Ti oxide depositsmay have formed in a similar fashion and that high concentrationsof phosphorus or carbon, or periodic fluctuation of fO₂ in themagma, are of secondary importance in ore formation. KEY WORDS: ELIP; Fe–Ti oxide ore; layered intrusion; Panzhihua; QUILF     

Composition and Assemblage Characteristics of Magnetic Minerals in Layer S_(5-1) of Xifeng and Duanjiapo Sections

Magneticmineralsintheloess paleosolseriesaccountforabout 1 % -2 %ofthetotal (LiuTungshengandZhangZhonghu ,1 962 ) .Duetotheiraerolianorigin ,themagneticmineralsarecomplicatedincomposition ,largeingrainsizerange ,andsignificantlydifferentincrystallinity .Asaresult,researchonthesemagneticmineralswouldbesetwithalotofdifficulties.Previousre searchersemployedopticalmicroscopic ,X raydiffractionandM ssbauerspectrometrictechniquestostudythemagneticmineralsintheloess paleosolseries,andchieflyontheb…     

纳米氧化物颗粒对水基钻井液润滑性能影响的试验研究

通过在水基钻井液中添加纳米氧化物颗粒,来改善其润滑性能。选用了Al2O3、TiO2及SiO2三种纳米氧化物颗粒作为钻井液改性添加剂,利用极压润滑仪及销盘摩擦磨损实验仪研究了添加不同种类和浓度纳米颗粒氧化物对水基钻井液的润滑性能及减摩效果的影响。结果表明,所添加的3种球形纳米颗粒均有润滑减阻减摩的效果,其中SiO2颗粒的钻井液的润滑性能、滤失性能以及减摩效果都是最好的。当纳米SiO2颗粒加量为0.4%时,滤失量最小,润滑系数降低率达到15.6%,摩擦系数降低率为32.0%,磨痕轨迹平滑,减摩效果最为明显。当纳米颗粒浓度超过0.5%时,减摩效果降低,磨盘脱层磨损明显。     

Geochemical Characteristics and Genetic Significance of Datangpo‐Type Manganese Ore Deposits during the Cryogenian Period

The Datangpo‐type manganese ore deposits, which formed during the Nanhuan (Cryogenian) period and are located in northeastern Guizhou and adjacent areas, are one of the most important manganese resources in China, showing good prospecting potential. Many middle‐to‐large deposits, and even super‐large mineral deposits, have been discovered. However, the genesis of manganese ore deposits is still controversial and remains a long‐standing source of debate; there are several viewpoints including biogenesis, hydrothermal sedimentation, gravity flows, cold‐spring carbonates, etc. Geochemical data from several manganese ore deposits show that there are positive correlations between Al₂O₃ and TiO₂, SiO₂, K₂O, and Na₂O, and strong negative correlations between Al₂O₃ and CaO, MgO, and MnO in black shales and manganese ores. U, Mo, and V show distinct enrichment in black shales and inconspicuous enrichment in Mn ores. Ba and Rb show strong positive correlations with K₂O in manganese ores. Cu, Ni, and Zn show clear correlations with total iron in both manganese ores and black shales. ∑REE of manganese ores has a large range with evident positive Ce anomalies and positive Eu anomalies. The Post Archean Australian Shale (PAAS) normalized rare earth element (REE) distribution patterns of manganese ores present pronounced middle rare earth element (MREE) enrichment, producing “hat‐shaped” REE plots. ∑REE of black shales is more variable compared with PAAS, and the PAAS‐normalized REE distribution patterns appear as “flat‐shaped” REE plots, lacking evident anomaly characteristics. δ¹³C values of carbonate in both manganese ores and the black shales show observable negative excursions. The comprehensive analysis suggests that the black shales formed in a reducing and quiet water column, while the manganese ores formed in oxic muddy seawater, which resulted from periodic transgressions. There was an oxidation–reduction cycle of manganese between the top water body and the bottom water body caused by the transgressions during the early Datangpo, which resulted in the dissolution of manganese. Through the exchange of the euphotic zone water and the bottom water, and episodic inflow of oxygenated water, the manganese in the bottom water was oxidized to Mn‐oxyhydroxides and rapidly buried along with algae. In the early diagenetic stage, Mn‐oxyhydroxides were reduced and dissolved in the anoxic pore water and then transformed into Mn‐carbonates by reacting with HCO₃^? from the degradation of organic matter or from seawater. In the intervals between transgressions, continuous supplies of terrigenous clastics and the high productive rates of organic matter in the euphotic zone resulted in the deposition of the black shales enriched in organic matter.