广西德保县荣华锰矿床地质特征研究

荣华锰矿赋存于桂西三叠系百逢组中,为该层位首次发现的中型规模锰矿。笔者通过参与矿区锰矿勘查工作,采用室内外观测、测试、工程揭露和验证等手段,对研究区地层、构造、沉积演化、含矿层位、矿体及矿石矿物特征、矿床成因和找矿标志等方面进行了分析探讨。研究发现荣华锰矿为典型的沉积-锰帽型矿床,严格受地层和构造因素控制;矿石类型主要为氧化锰矿贫锰矿石;氧化锰矿物主要为水羟锰矿、硬锰矿及软锰矿;矿床成因与原始沉积作用、后期风化淋滤等有重要关系;百逢组浊积岩之下、罗楼组碳酸盐岩之上的狭窄范围是荣华锰矿的典型找矿标志,该标志对大量出露三叠系百逢组的桂西地区具有普遍意义,同时指出桂西地区该组地层内具有良好的找矿前景。     

鄂西走马地区南华纪古城期-南沱早期古气候和古氧相演化：来自细碎屑岩元素地球化学的证据

新元古代后期地球经历了至少两次全球规模的冰川期,分别为Sturtian冰期和Marinoan冰期。鄂西走马地区南华系古城组与南沱组分别属于Sturtian和Marinoan冰期沉积,大塘坡组代表间冰期沉积,同时,大塘坡期是我国重要的成锰时期。本文通过对走马地区ZK702钻孔岩心古城组、大塘坡组、南沱组底部细碎屑岩样品元素地球化学的研究,计算了CIA、CIW、PIA、Al/Ca、Rb/Sr、V/Cr、U/Th等特征值,探讨了该区南华纪冰期至间冰期的古气候和古氧相演化过程,结合岩石学证据认为：古城冰期气候寒冷干燥(CIA值从底部的69. 2过渡至57. 8,均值为62. 2),大塘坡间冰期早期气候依然寒冷(CIA值介于54. 3～62. 7,均值59. 7),大塘坡中晚期气候恢复温暖湿润并趋于稳定(CIA值介于70. 2～81. 1,均值75. 8),南沱冰期气候又转向寒冷干燥(CIA值由78. 6降低至61. 9),CIW、PIA、Rb/Sr值等指标反映的古气候演化过程与CIA值反映一致,Al/Ca值的变化也反映了陆源碎屑输入量随着古气候波动;V/Cr、U/Th、Ni/Co等比值反映出研究区古海洋古城期-南沱早期总体处于氧化环境,其中大塘坡早期处于弱氧化环境,古城期、大塘坡中晚期和南沱早期处于氧化环境;研究区大塘坡锰矿形成于间冰期早期寒冷气候下的弱氧化环境,气候转暖后锰矿停止沉积,锰矿成矿与古气候和古氧相具有耦合关系。     

锰矿主要类型、分布特点及开发现状

锰的用途非常广泛,世界上90%～95%的锰应用于冶金工业,其余应用于电池工业、陶瓷工业、化学工业等。根据成矿作用过程中的含矿岩系特征,将世界锰矿划分为海相沉积型、火山(热液)-沉积型、变质型、热液型和表生型5类,以海相沉积型、变质型和表生型为主。截至2019年,世界锰的储量达8.12亿t,但分布极不均匀,主要集中在南非、巴西、乌克兰、澳大利亚、加蓬、中国、印度、加纳等国,而优质锰矿石主要分布在南非、澳大利亚、加蓬、加纳。时间上,将锰的成矿作用分为7期,其中元古宙和新生代是主要的成矿期。空间上,锰矿床主要分布在南非德兰士瓦群、乌克兰尼科波尔盆地、澳大利亚格鲁特岛和皮尔巴拉克拉通、中国泛扬子区、西非克拉通等。目前,锰的生产主要集中在南非的卡拉哈里和波斯特马斯堡锰矿田、澳大利亚的格鲁特岛、加蓬的莫安达锰矿、加纳的恩苏塔锰矿等地。     

地源热泵系统中水泥基灌浆材料性能优化

分别考察了水灰比、砂灰比、粗钢渣代砂率、钢渣粉代水泥率和泥浆掺入率对灌浆材料的工作性能、导热性能和固结强度的影响.研究结果表明:在未加废钢渣(包括粗钢渣和钢渣粉)前提下,若水灰比为0.55 ～0.6、砂灰比为2～2.2时,灌浆材料的综合性能最好;若单独用粗钢渣替代砂,单独用微米级钢渣粉替代水泥,并且粗钢渣代砂率和钢渣粉代水泥率分别控制在40％和20％以内时,便能保证灌浆材料良好的综合性能;增大泥浆掺入率可提高灌浆材料的工作性能,但会降低其导热性能和固结强度,因此泥浆掺入率需控制在10％以内才能保证灌浆材料有足够的导热性能和固结强度.结果表明,工业废弃物的再利用,可为地源热泵工程节约24.84％的原材料成本.     

Geochemistry and Origin of Ananai Stratiform Manganese Deposit in the Northern Chichibu Belt, Central Shikoku, Japan

Abstract. Major and trace element contents are reported for Permian manganese ore and associated greenstone from the Ananai manganese deposit in the Northern Chichibu Belt, central Shikoku, Japan. The manganese deposit occurs between greenstone and red chert, or among red chert beds. Chemical compositions of manganese ore are characterized by enrichments in Mn, Ca, P, Co, Ni, Zn, Sr and Ba, and negative Ce and positive Eu anomalies relative to post-Archean average Australian Shale (PAAS). Geochemical features of the manganese ore are similar to those of modern submarine hydrother-mal manganese deposits from volcanic arc or hotspot setting. In addition, geochemical characteristics of the greenstone closely associated with the Ananai manganese deposit are analogous to those of with-in plate alkaline basalt (WPA). Consequently, the Ananai manganese deposit was most likely formed by hydrothermal activity related to hotspot volcanism in the Panthalassa Ocean during the Middle Permian. This is the first report documenting the terrestrially-exposed manganese deposit that was a submarine precipitate at hotspot.     

矿渣微细粉掺量对水泥水化产物的影响

利用X射线衍射、TG-DSC综合热分析以及环境扫描电子显微分析技术等,研究了矿渣微细粉对水泥水化产物钙矾石、Ca(OH)₂、CSH凝胶等的影响规律。研究结果表明,在水化早期,矿渣微细粉即参与水泥水化进程,显著影响水泥水化产物钙矾石、Ca(OH)₂和CSH凝胶等的生成速度和生成量及微观形貌,并且随着其掺量增大及水化时间延长,矿渣微细粉参与水泥水化反应程度逐渐提高。     

Geochemical types of pacific polymetallic nodules: An application of multivariate analysis

A total of 843 samples of Pacific Ocean polymetallic nodules (PNs) from five survey areas have been studied (metals analyzed: Mn, Fe, Ni, Cu, Co, Zn, Pb). The statistical analysis included the following techniques: factor R analysis, quick cluster Q analysis into 50 preclasses, various hierarchical cluster Q analyses (HCAs) using the preclasses (application of different HCAs to an identical set of data and of an identical HCA to two different subsets of the data), comparison of the HCA. The PNs of the survey areas can be grouped into five geochemical types (I‐V). The genesis of the PNs was interpreted as early diagenetic, hydrogenetic, and mixed (early diagenetic/hydrogenetic and hydrogenetic/hydrothermal. In addition, some further conclusions regarding the applicability of various HCA techniques depending on the structure of the data set have been drawn.     

鄂东北早元古代沉积变质锰矿元素矿物组合特征

鄂东北早元古代沉积变质锰矿是我国时代最古老的锰矿之一,是由早元古代锰质碳酸盐岩经区域变质作用而成,后又经风化富集形成工业矿床。由于特殊的地质构造背景和成矿作用的多阶段性,元素和矿物组合复杂,具有独特性。本文研究了各种组分的演变关系和元素集散因素,为锰质碳酸盐岩在高压绿片岩相区域动力变质及其后表生作用中的演变提供了一个实例。     

锰矿石中硅酸锰的分离和测定方法对比

文章对几种分离测量硅酸锰的方法进行了对比。指出硅酸锰测定失真的缘由。选择了浸取分离伴生铁矿物的浸取剂及浸取分离条件。     

Experimental Study of Gold and Platinum Solubility in a Complex Fluid under Hydrothermal Conditions

Abstract: The solubility of gold was studied in water and aqueous NaCl (1– 5 m) solutions under oxygen and sulfur buffered conditions between 300–500C at a constant pressure 1 kb. Two buffer assemblages HMP and PPM were used. Analysis of the scatter in measured values in log m_Au–m_NaCl–T frame fixed linear dependence between log m_Au and T at any studied iso‐pleth (m_NaCl) in the form of log m_Au = a. T(C) + b. Coefficients of the equation were calculated for water and NaCl (1, 3, 5 m) solutions. The maximum solubility characterizes the NaCl‐free system in the presence of HMP. In the case, Au solubility increases from (log m_Au) –6. 72 to –5. 04 at 300 and 500C, respectively. In the presence of PPM, maximum of Au solubility was obtained for the 5 mNaCl solution. In a similar manner solubility rises from –6. 54 to –5. 77 at 300 and 500C, accordingly. In studied f_O2/f_S2 area the behavior of Au solubility testified that: (i) – a composite interaction between chloride and hydrosulfide speciation of gold affects its total solubility; (ii) – in addition of NaCl up to about 1. 5 m the solubility decreases, more pronounced in the presence of HMP; (iii) – the contribution of chloride in total Au solubility is more for PPM despite of lower f_O2value, than for HMP. The solubility of platinum was studied in the Pt–Cl–S–H₂O system between 300 and 500C, 1 kb. PPM solid buffer controlled oxidation state, pH and sulfur activity of solutions (H₂O, 1 mNaCl and 0. 1 mHCl). Under the conditions, PtS precipitated from the solutions with increasing temperature and acidity. The PtS solubility in the 0. 1 m_HCl solutions lowers slightly in the range of 300–500C from –5. 30 to –5. 60 (in log m_Pt) that is typical to the hydrosulfide species. It was deduced that reducing media, regulated by the PPM assemblage, suppress activity of chloride species of Pt. More oxidizing conditions were modeled in runs using mixtures of Mn(II), Mn(III) and Mn(IV) oxides to buffer the aqueous‐chloride solutions between 300 and 500C, 1 kb. It was found that MnO tends to oxidize at T below 400C forming intermediate Mn‐hydroxides (β–MnOOH, Mn (OH)₂ and Mn₂(OH)₃Cl). These phases are metastable and transfer to Mn₃O₄ with increasing duration. Generation of the Mn‐hydroxides leads to a change of physical‐chemical parameters of the solutions, such as water activity, pH and Eh. The last results in abrupt increase in the noble metals dissolution. At stable existence of only Mn₃O₄, the solubility of both Pt and Au lowers to equilibrium values. Essential catalysis effect of Pt on intensity and rate of Mn(II) oxidation was found. The dominant role of chloride of Pt and Au was defined under most oxidized conditions, specified by Mn₂O₃–MnO₂ buffer. So at 400C, dissolved Au (log m_Au) increases from –4. 40 in water to –1. 00 in 0. 1 m_HCl, and ones of Pt (log m_Pt) from –4. 80 to –2. 90 accordingly. Thus, mixing of hydrosulfide and chloride solutions, as well as transformation of the systems to the stable state act upon total solubility of the noble metals.