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塔里木盆地东部的罗布泊盐湖和柴达木盆地西部的盐湖分别位于阿尔金山两侧,均产出有大量富钾卤水,在油气藏开采中还伴随产出富钾油田水.为探讨阿尔金山两侧盐类资源富集机制及其控制因素,综合分析了罗布泊盐湖、柴达木盆地西部盐湖以及油田水的水化学和氢氧同位素地球化学特征,发现:富钾卤水的形成除依靠地表汇入水体的蒸发浓缩作用外,罗布泊晶间水、柴达木晶间水和油田水氢氧同位素均可演化至δD=-30‰,δ18 O=7.5‰左右,可能是深部流体上涌补给的结果.同时,根据87 Sr/86 Sr值并结合δ11 B、3 He/4 He同位素特征确认了盐湖成矿与深部流体有关,且指示罗布泊盐湖更具深源特征.深部流体对于两侧盆地成盐富钾有关键性作用,罗布泊盐湖可能接受深部流体补给,柴达木盆地西部富钾盐湖卤水多数可接受油田水的补给,而少部分可能接受深部流体补给. 相似文献
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四川盆地地下卤水资源丰富,尤其川东北地区地下卤水富含高品质钾资源。本项目以四川普光地区富钾卤水为研究对象,根据卤水组成,采用模拟计算并结合实验验证的方法,研究了高温蒸发时,氯化钠、氯化钾、光卤石、硼酸等矿物的析出阶段及特点。研究结果表明,当蒸失水率约80%时,体系中约85%的NaCl析出,同时KCl达到饱和,继续蒸发可获取钾石盐。控制总蒸失水率94%~95%时分离,体系中大于80%的钾可在这一阶段析出,且湿基中KCl品位可高达约45%;析出钾石盐后的卤水降至室温可获得NaCl、KCl、KCl·MgCl2·6H2O及H3BO3的混合物,硼的析出率可达到约80%。同时,研究表明,将蒸失水率约80%时分离石盐后的卤水直接降温可以获得湿基品位约高达70%的钾石盐矿,钾析出率约50%。综合对比分析,提出两条以钾资源开发为主的工艺路线:其一为“高温蒸发析氯化钠-高温蒸发析氯化钾-冷却析钾硼混盐”,通过加工获得KCl及H3BO3产品;其二为“高温蒸发析氯化钠-冷却析钾”,通过加工获得高端KCl产品。 相似文献
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四川盆地中三叠统雷口坡组中发育多种类型的钾盐矿藏,是我国找钾的重点目标层系。磨溪气田雷口坡组地层卤水富含K、Li、Br、B元素,定性为中低矿化度KCl、LiCl、Br-、B2O3等超标的优质化工原料水,显示出较好的钾盐勘探前景。地震资料解释结果表明,磨溪气田雷口坡组一段的第一亚段(雷一1)顶面表现为一个完整的长轴背斜形态,断层不发育。富钾卤水发育在背斜的翼部,而天然气则占据了背斜的核部,二者共同贮存在雷一1亚段溶蚀孔洞发育的滩相白云岩中,构成了典型的同层型气钾复合矿藏。借鉴含油气系统的概念,将富钾卤水的形成、聚集及后期保存等影响卤水型钾矿形成全过程的各种因素总结归纳为6大关键要素,即钾的物质来源,储层物性、封盖条件、圈闭条件、运移方式和保存条件。在乐山—龙女寺古隆起形成和演化的背景下,确定构造圈闭形成时间,分析优质储层发育有利因素以及后期保存条件,并按照各要素在时空上的搭配关系,动态地分析雷口坡组同层型气钾复合矿藏的形成过程。烃类物质和卤化物都是地下水所含的特殊物质,在地下水动力场的作用下,地层水在雷口坡组内部向着川中地区的继承性发育的古构造高点——磨溪背斜持续运移。被运移而来的由蒸发浓缩的古海水和石膏脱水形成的初始富钾地层水不断捕获下伏绿豆岩释放的钾离子,使得钾离子二次富集成藏。在地层水运移和气藏压力的共同作用下,形成气在上、富钾卤水在下的复合矿藏。长期继承性发育的古隆起不仅是油气聚集的有利部位,亦是二次运移、聚集的富钾卤水矿藏发育部位。本次研究成果为四川盆地及其他类似盆地的“气钾兼探”工作提供了一种新的方法和思路。 相似文献
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To unravel the mystery of the relationship between evaporates, Ca–Cl brines and accumulations of oil and N2 in the basins of ancient cratons, their N2, CH4 and He concentration ratios, as well as the isotopic composition (δ15N, δ13C and 3He/4He) were compared within the Volga-Ural basin. The study allowed subsalt fluids from Volga-Ural Basin to divide into two genetic groups. The first one is found within the basin's platform area. It includes Ca–Cl brines, high-viscosity heavy oil, bitumen and N2, which has concentrations higher than that of CH4 and positive values of δ15N. The second one is tied to the edge of the platform, the Ural Foredeep and Peri-Caspian Depression. In this group, only the oil and gas reservoirs, which have more CH4 than N2, and possibly negative values of δ15N, were discovered. Interaction of gas components in compared fluids indicates great role of degassing in the formation of their composition. It is suggested that the fluids of the first group (N2 > CH4) is what remains, and the second group (N2 < CH4) is what is disappears from the rocks during their metamorphism and degassing. 相似文献
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基于相化学研究老挝万象钾镁盐矿床形成的机制 总被引：2，自引：0，他引：2
老挝万象钾镁盐矿床是一个典型的海相碎屑盐缺硫酸盐型钾盐矿床, 该矿床形成于古近纪, 是古海水蒸发浓缩沉积形成。老挝万象钾镁盐矿床中缺乏硫酸盐和碳酸盐沉积物, 因此深入研究该矿床的形成机制很重要。本文研究探讨了该矿床形成时的古海水特点, 根据相化学, 分析成钾原始卤水的物理化学特性, 从矿体形成的化学基础来研究老挝钾镁盐矿床形成的机制。结果表明: 显生宙以来海水组分发生变化, 经海相非骨骼灰岩和钾盐蒸发岩矿物学研究, 发现这两种沉积岩长期以来连续变化, 在“文石海”是MgSO4型蒸发盐, 在“方解石海”是KCl型蒸发盐, 从白垩纪晚期、第三纪早期的底部石盐溴含量及矿物学特征表明, 此时处于“方解石海”, 古海水组分的特点是造成缺硫酸盐型钾盐矿床形成的物化基础; 通过NaCl-KCl-MgCl2-H2O和NaCl-KCl-MgCl2-CaCl2-H2O两个体系相图的分析认为, 当时所形成的成钾原始体系母液是高镁、低钾氯化物型的卤水, 在母液蒸发过程中, 由于原始海侵母液与残余高镁母液的掺杂作用, 致使结晶路线直接从氯化钠区到E点母液或光卤石与氯化钠共饱线上, 而没有通过氯化钠和氯化钾的共饱线, 因而在矿体中氯化钾相很少或几乎不存在, 由于外界CaCl2型水体的掺杂, 使成钾母液进入光卤石相区, 随着蒸发的进行, 最终形成溢晶石矿物。 相似文献
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《Chemie der Erde / Geochemistry》2014,74(3):425-441
Sources and mineralization of groundwaters from Cretaceous A7/B2 and B4 limestone aquifers in the Golan and Ajloun Heights are derived from conjoint discussion of stable isotopes of water and sulphate, major ion chemistry, rare earth distribution patterns and the (hydro)geological setting. Isotope fractionation of precipitation was used to derive elevation and continental influence of recharge areas. Positive shift of δ18O and δ2H occur due to evaporation before replenishment and the interaction with basalts. Major infiltration areas for Golan Heights are the limy foothills of the Mt. Hermon and for the Ajloun Heights the Plateau itself. To a less degree, precipitation infiltrates also the basaltic catchments. Groundwaters are mineralized by water/rock (i) variably altered limestones by diagenesis, (ii) evaporates and seawater brines enclosed in limestone matrix and (iii) locally occurring basaltic intrusiva. In the Yarmouk Gorge, a deep-seated brine of the Ha’on type ascends and mixes with the fresh shallow groundwater.Contrasting the macro chemical composition, REY distribution patterns indicate the lithology of the recharge areas. Infiltration over basalts results in REY patterns distinctly different to those derived from limy catchments.REY and isotope fingerprints prove that water from the Syrian Hauran Plateau is recharging springs and wells in the lowermost Yamouk gorge. The basaltic cover of the Golan Heights is of minor importance for recharge of the underlying A7/B2 aquifer, which becomes recharged at the foothills of Mt. Hermon and gets confined southwards. Even the wells in the basaltic cover receive water from the underlying limestone aquifer.Anomalous heat flux near the Yarmouk gorge and locally in the western escarpment of the Ajloun may be produced by ascending fluids from greater depth and/or by basaltic intrusions. 相似文献
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正Identification of the favorable salt-and potash-forming layer,we still mainly rely on logging interpretation and coring verification.However,we both know that the continuously carbonate platform is cyclical growing.It has recorded valuable information about the phase transition of carbonate rocks,which were synchronized with the relative sea-level cycles.This paper presents a fast and 相似文献
9.
关于江陵凹陷富钾卤水的物质来源和成因机理仍未查明. 对凹陷新生代玄武岩开展矿物学、岩石学、地球化学研究以及水-岩反应模拟实验,重点研究时间、温度、流体成分等对水-岩反应的影响. 结果表明,卤水具有高锂低镁的特征,说明其在成因上受到火山活动的影响;研究区岩浆发生不同程度的分异,玄武岩蚀变作用强烈,表明地下热液的交代作用强烈,玄武岩通过水-岩反应为富钾卤水矿提供了物质来源;温度是流体对元素的淋滤能力的主要控制因素,高盐度流体是各成矿元素主要的迁移载体,水-岩反应是卤水形成的重要过程. 相似文献
10.
Solubility of Anhydrite, CaSO4, in NaCl-H2O Solutions at High Pressures and Temperatures: Applications to Fluid-Rock Interaction 总被引：1，自引：0，他引：1
Anhydrite solubility in H2O–NaCl solutions was measuredat 6–14 kbar, 600–800°C and NaCl mole fractions(XNaCl) of 0–0·3 in piston–cylinder apparatus.Solubilities were determined by weight changes of natural anhydritein perforated Pt envelopes confined with fluid in larger Ptcapsules. In initially pure H2O at 10 kbar and 800°C, CaSO4concentration is low (0·03 molal), though much largerthan at the same temperature and 1 kbar. Hematite-buffered experimentsshowed slightly lower solubilities than unbuffered runs. CaSO4solubility increases enormously with NaCl activity: at 800°Cand 10 kbar and XNaCl of 0·3, CaSO4 molality is 200 timeshigher than with pure H2O. Whereas CaSO4 solubility in pureH2O decreases with rising T at low T and P, the high-P resultsshow that anhydrite solubility increases with T at constantP at all XNaCl investigated. The effects of salinity and temperatureare so great at 10 kbar that critical mixing between sulfate-richhydrosaline melts and aqueous salt solutions is probable at900°C at XNaCl 0·3. Recent experimental evidencethat volatile-laden magmas crystallizing in the deep crust mayevolve concentrated salt solutions could, in light of the presentwork, have important implications regarding such diverse processesas Mount Pinatubo-type S-rich volcanism, high-f O2 regionalmetamorphism, and emplacement of porphyry Cu–Mo ore bodies,where anhydrite–hematite alteration and fluid inclusionsreveal the action of very oxidized saline solutions rich insulfur. KEY WORDS: anhydrite; sulfur; solubility; metamorphic brines; granulites 相似文献