Phase Equilibria of Salt-water Systems Containing Magnesium and Borate Ions

正1 Introduction A salt lake is a naturally occurring complex body of water and salt interaction.More than 700 salt lakes are widely distributed in the area of the Qinghai-Tibet Plateau.Most of the salt lakes are famous for their abundance of lithium,potassium,magnesium,and boron resources.It is     

Study on the Isothermal Evaporation Process at 5℃ with the Brine of Laguocuo Salt Lake

正1 Introduction Tibet has nurmerous salt lakes.Laguocuo is one of the salt lakes,which is located to the sorthern of Ali Plateau,31°59′02″N-32°04′08″N,84°02′03″E-84°12′03″E.Its lake water is rich in potassium,magnesium,lithium,boron,rubidium,cesium and other resources.The study of     

原子吸收分光光度法快速测定铬铁矿中钙、镁、锰

通过在标液中加入相应的Sr来消除离子干扰,采用原子吸收分光光度法快速测定CaO、MgO、MnO的含量,方法经国家标准物质验证,其RSD<2%(n=6)。其结果与标准值相符。方法达到了准确、简便、快速、实用性强。     

偏硼酸锂溶液物种分布和物化性质

测量了不同浓度LiBO2溶液分别在298.15和323.15 K的密度、电导和pH,通过测得的pH和硼酸根离子化学平衡常数计算得到溶液中硼酸根离子的物种分布。根据获得的物种分布结果,推测溶液中各硼酸根离子之间的相互转化过程,并分别用偏摩尔体积公式和Onsager方程对溶液偏摩尔体积及摩尔电导率进行计算并拟合。对计算得到偏摩尔体积值和极限摩尔电导率值与文献报道的数据进行对比,计算结果与文献报道值吻合较好。     

俯冲带中大理岩与榴辉岩的Mg-Fe-C-O同位素迁移

碳酸盐岩和碳酸盐化岩石是俯冲带中碳的主要地质载体.俯冲-折返的超高压变质岩记录了俯冲隧道中流体-岩石的相互作用与元素迁移,是研究地球内部元素循环的重要媒介.本文采集了大别造山带罗家岭互层状产出的大理岩和榴辉岩,建立了横跨岩性界面的矿物组成、显微结构和Mg-Fe-C-O同位素剖面.大理岩中主要组成矿物为白云石,其次为方解...     

敞开酸溶和偏硼酸锂碱熔ICP-MS法测定多金属矿中的稀土元素及铌钽锆铪

用电感耦合等离子体质谱法(ICP-MS)测定地质样品中的稀土及难熔元素,混合酸敞开酸溶法和碱熔融法是两种主要的溶样方法。但地质样品组分复杂,元素之间存在相互共生的现象,对于特殊元素、特殊样品用传统酸溶法会造成部分元素消解不完全,使测定结果不准确;而碱熔法的操作过程繁琐,且溶液盐度高,易产生基体干扰和堵塞仪器进样系统。本文改进了传统四酸和五酸体系,采用氢氟酸-硝酸-硫酸敞开酸溶体系,用国家一级标准物质制作标准曲线测定15种稀土元素,方法准确度(ΔlgC)为0.001～0.027。同时改进了偏硼酸锂碱熔法,样品用偏硼酸锂碱熔提取,加入氢氧化钠调节溶液至碱性条件,所测元素与偏硼酸锂共沉淀后过滤分离熔剂,再用硝酸复溶测定15种稀土元素及铌钽锆铪。两种溶样方法的测定值与认定值的相对误差为1.09%～9.30%。将混合酸敞开酸溶法测定稀土元素、偏硼酸锂碱熔法测定铌钽锆铪的结果与其他实验室密闭酸溶法相比,两组数据的相对偏差为0.13%～15.32%。本实验表明,混合酸敞开酸溶法适用于测定地质样品中的稀土元素,偏硼酸锂碱熔法不仅适用于测定地质样品中的稀土元素及铌钽锆铪,也适用于测定如古老高压变质岩石及铝含量高的样品中的铌钽锆铪。     

Evaluating new fault-controlled hydrothermal dolomitization models: Insights from the Cambrian Dolomite,Western Canadian Sedimentary Basin

Fault-controlled hydrothermal dolomitization in tectonically complex basins can occur at any depth and from different fluid compositions, including ‘deep-seated’, ‘crustal’ or ‘basinal’ brines. Nevertheless, many studies have failed to identify the actual source of these fluids, resulting in a gap in our knowledge on the likely source of magnesium of hydrothermal dolomitization. With development of new concepts in hydrothermal dolomitization, the study aims in particular to test the hypothesis that dolomitizing fluids were sourced from either seawater, ultramafic carbonation or a mixture between the two by utilizing the Cambrian Mount Whyte Formation as an example. Here, the large-scale dolostone bodies are fabric-destructive with a range of crystal fabrics, including euhedral replacement (RD1) and anhedral replacement (RD2). Since dolomite is cross-cut by low amplitude stylolites, dolomitization is interpreted to have occurred shortly after deposition, at a very shallow depth (<1 km). At this time, there would have been sufficient porosity in the mudstones for extensive dolomitization to occur, and the necessary high heat flows and faulting associated with Cambrian rifting to transfer hot brines into the near surface. While the δ¹⁸O_water and ⁸⁷Sr/⁸⁶Sr ratios values of RD1 are comparable with Cambrian seawater, RD2 shows higher values in both parameters. Therefore, although aspects of the fluid geochemistry are consistent with dolomitization from seawater, very high fluid temperature and salinity could be suggestive of mixing with another, hydrothermal fluid. The very hot temperature, positive Eu anomaly, enriched metal concentrations, and cogenetic relation with quartz could indicate that hot brines were at least partially sourced from ultramafic rocks, potentially as a result of interaction between the underlying Proterozoic serpentinites and CO₂-rich fluids. This study highlights that large-scale hydrothermal dolostone bodies can form at shallow burial depths via mixing during fluid pulses, providing a potential explanation for the mass balance problem often associated with their genesis.     

新型抗水氯氧镁水泥防渗渠在自然环境的水化产物、相转变规律及其对强度的影响

氯氧镁水泥(Magnesium oxychloride cement, MOC)具有快凝、早强、高强、防火和不腐蚀玻璃纤维等优点,非常适合于制作玻璃纤维增强薄壁制品,在农业灌溉工程中具有良好的应用前景。采用XRD和TOPAS分析了新型抗水氯氧镁水泥制成内蒙古防渗渠的物相组成,探讨了氯氧镁水泥制品在自然环境的水化产物与相转变规律、以及相组成对强度的影响。结果表明,在水分缺少的条件下,氯氧镁水泥的水化产物主要为5Mg(OH)_2·MgCl_2·8H_2O(5·1·8)和Mg(OH)_2;在水分充足的条件下,水化产物主要为Mg(OH)_2和5·1·8,碳化产物为碳化氯氧化镁Mg(OH)_2·MgCl_2·2MgCO_3·6H_2O(1·1·2·6)和水菱镁矿4MgCO_3·Mg(OH)_2·4H_2O(4·1·4)。水化产物对强度有促进作用,而碳化产物会降低强度。通过10年的工程环境考验,证明新型氯氧镁水泥制品在环境中能够保持主要强度相5·1·8的稳定性,具有良好的长期力学性能。     

山西省盂县羊泉冶镁白云岩矿床地质特征、成因及经济意义研究

金属镁是新世纪重要的绿色金属能源,而冶镁白云岩是生产金属镁不可缺少的原料,是山西省能源重化工基地的一种十分重要的矿产资源.盂县羊泉冶镁白云岩矿床位于吕梁、太行断块-五台山块隆东侧,白云岩矿体赋存于寒武系上统-奥陶系下统三山子组,总体上呈走向NW、倾向SW的单斜构造.含矿岩石主要为中-厚层细-粗晶白云岩,粉晶-细晶或中粗晶粒状结构,块状或薄层状构造.矿床的形成演化经历了沉积-白云岩化-重结晶三个阶段.矿体平均品位ω(MgO)为21.20％、ω(SiO2)为0.67％、ω(K2O+ Na2O)为0.076％,品位变化较均匀.该区共求得冶镁用白云岩矿资源量约3.45亿吨,属一大型矿山,具有较大的开发前景.     

活性MgO定量分析标准方法的比较研究

用WB和JC标准水合法测定轻烧MgO粉的活性MgO含量,对测定结果进行方差和误差分析,并研究了水化时间对测定结果的影响。结果表明,两种方法存在显著性差异,WB和JC水合法的平均相对误差分别为1.31%和-19.85%,WB水合法精密度远高于JC水合法。以WB水合法为基准,JC水合法的平均相对误差大于-20%,远远超过行业标准中规定的±3%。因此,对于镁水泥原料MgO中活性含量的定量分析,不能采用JC方法,必须采用WB方法。此外,发现水化3 h已经接近活性氧化镁的水化平衡,为修订WB标准方法提供了参考依据。