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1.
智利北部阿塔卡马富锂干盐湖地质   总被引：1，自引：0，他引：1  
智利北部阿塔卡马干盐湖位于一个内陆闭流构造盆地中，形成于晚第三纪。从中新世至今，全地内有强烈的火山作用。它是智利最大的干盐湖，也是世界上最大的富锂干盐湖之一。其盐矿物和卤水（包括锂）的物质来源如下；（１）火山活动形成的大量流纹岩质火山灰流凝灰岩，并伴随着大量地热水；（２）从火山岩中淋滤的可溶盐；（３）淋滤富锂粘土岩；（４）安第斯山东部湖和干盐湖的盐卤水沿着上新世（？）至第四纪形成的山前断裂流入阿塔卡马盆地，再通过沙漠环境的长期蒸发，因此盆地内积累了大量盐组分。  相似文献   

2.
Diagenetic-hydrothermal brines, here called “hydrothermal Ca–Cl brines,” have compositions that reflect interactions between groundwaters and rocks or sediments at elevated temperatures. Hydrothermal Ca–Cl brines reach the surface by convection-driven or topographically driven circulation, and discharge as springs or seeps along fault zones to become important inflow waters in many tectonically active closed basins. Case studies from (1) Qaidam Basin, China, (2) Death Valley, California, (3) Salar de Atacama, Chile, and (4) Bristol Dry Lake, California illustrate that hydrothermal Ca–Cl inflow waters have influenced brine evolution in terms of major ion chemistries and mineral precipitation sequences. All four basins are tectonically active; three (Death Valley, Salar de Atacama, and Qaidam Basin) have well-documented Ca–Cl spring inflow and Holocene faulting. Bristol Dry Lake has young volcanic deposits and Salar de Atacama has an active stratovolcano on its eastern margin, indicating subsurface magma bodies. A midcrustal magma chamber has been identified in southern Death Valley. Volcanism and faulting in these closed basins provides the heat source for hydrothermal-diagenetic processes and the energy and pathways to deliver these waters to the surface.  相似文献   

3.
The transfer of reactive bromine into the atmosphere was recently observed by Hönninger et al. [Hönninger, G., Bobrowski, N., Palenque, E.R., Torrez, R., Platt, U., 2004. Reactive bromine and sulfur emission at salar de Uyuni, Bolivia. Geophys. Res. Lett.31, doi:10.1029/2003GL018818] in a large salt pan of the Bolivian Altiplano: the salar de Uyuni. However, bromide is considered to be an excellent conservative tracer, which leads to the questioning of its actual conservation in surficial geochemical processes. The relation between bromide and lithium, thought to be a conservative component in waters and brines of the Central Andes, points to a depletion of Br relative to Li in Uyuni brines of about 50-300 kg/day, a flux close to that measured by Hönninger et al. (2004): ?200 kg/day. Such values are very low in regard to the size of the salar (5-30 g/km2/day). Salt efflorescences have a much higher surface area than a flat salt crust, which should enhance the release of bromine. Leach solutions of salt efflorescences in closed basins of northern Chile are compared to their parent waters. Conservative components should have the same concentration ratios in both solutions. Actually, a strong depletion in Br is observed in the leach solutions, which could suggest a significant release of Br from the salt into the atmosphere. During the rainy season, efflorescences are leached and their dissolved components brought in saline lakes and salars. Evaporative profiles show a slight but noticeable fractionation between Li and Br which could be due to the contribution of Br-depleted leach solutions of salt efflorescences. Therefore, bromide does not behave conservatively in surface waters and brines of the Central Andes. If the loss of Br is really due to its transfer into the atmosphere, then the flux would be much higher than that estimated for the salar de Uyuni alone. Numerous salt pans, saline lakes, and widespread efflorescences covering large land surfaces would contribute significantly more reactive bromine into the atmosphere.  相似文献   

4.
We present results of a comprehensive study of ground ice, saline waters, and brines in the cryoartesian basins of the northeastern Siberian Platform. The composition of major geochemical types of ground ice is considered. The specifics of the hydrogeochemical zonation of the cryoartesian basins are the regional distribution of chloride saline waters and brines. Study of stable isotopes (18O, D, 37Cl, 81Br, and 87Sr/86Sr) led us to the conclusion that the chloride brines resulted either from the leaching of halogen rocks or from the metamorphism of bittern connate water. The drainage brine reserves (hydromineral resources) of the Udachnaya kimberlite pipe in the Olenek cryoartesian basin are assessed.  相似文献   

5.
《Applied Geochemistry》2001,16(6):609-632
Generally, the history of past sub-surface fluid movements is difficult to reconstruct. However, the composition of oil-field waters characterizes the origins and mixing processes that allow such a reconstruction. We have investigated present-day formation waters from Brent Group sedimentary rocks of the Oseberg Field in order to assess both their geochemical variations, and their origin(s). Water samples (sampled at the separator) produced from immediately above the oil–water contact and from the aquifer (water-saturated zone below the oil–water contact) were taken from 11 wells across the field. In addition, 3 trace water samples were extracted from oil produced from higher up in the oil column. The water samples were analysed for their chemical components and isotopic compositions. Conservative tracers such as Cl, Br, δD, and δ18O were used to evaluate the origin of the waters. All formation waters can be characterised as Na–Cl-brines. The separator samples are of aquifer origin, indicating that aquifer water, drawn up by the pressure reduction near the well, is produced from the lower few tens of metres of the oil-zone. By defining plausible endmembers, the waters can be described as mixtures of seawater (60–90%), meteoric water (10–30%), evaporated seawater (primary brines) (3–5%), and possibly waters which have dissolved evaporites (secondary brines). Alternatively, using multidimensional scaling, the waters can be described as mixtures of only 3 endmembers without presupposing their compositions. In fact, they are seawater, very dilute brine, and a secondary brine (confirming the power of this approach). Meteoric water was introduced into the reservoir during the end-Brent and early-Cretaceous periods of emergence and erosion, and partially replaced the marine pore fluids. Lateral chemical variations across the Oseberg Field are extremely small. The waters from closer to the erosion surfaces show slightly stronger meteoric water isotopic signatures. The primary and secondary brines are believed to come from Permian and Triassic evaporitic rocks in the deeply buried Viking Graben to the west, and to have been modified by water–rock interactions along their migration path. These primary basinal brines have not been detected in the oil–zone waters, suggesting that the brines entered the reservoir after the main phase of oil-migration. There are indications that these external fluids were introduced into the reservoir along faults. Present-day aquifer waters are mixtures of waters from different origins and hardly vary at a field-scale. They are different in composition to the water trapped in the present oil-zone. One of the oil-zone samples is a very dilute brine. It is thought to represent a simple mixture of seawater and meteoric water. Due to oil-emplacement, this geochemical signature was preserved in the waters trapped within the oil-zone. Another oil-zone water shows a very similar chemical signature to the aquifer waters, but the chlorine isotopic signature is similar to that of the dilute oil-zone water. This water is interpreted to represent a palaeo-aquifer water. That is, it was within the aquifer zone in the past, but was trapped by subsequent emplacement of more oil. These vertical differences can be explained by two features: (i) emergence of the Brent Group sedimentary rocks in the Early Cretaceous allowed ingress of meteoric water; (ii) subsequent rapid burial of Viking Graben rocks caused migration of petroleum and aqueous fluids into the adjacent, less deeply buried Oseberg Field.  相似文献   

6.
Thermal waters of northern (18°–27°S) and southern (37°–45°S) Chile occur in two very different climatic, geologic and hydrologic environments: arid closed basins with abundant evaporites in the north; humid climate and well drained valleys in the south. The origin and behavior of the main components of the two groups of waters are examined and compared to each other. The modeling of the alteration of volcanic rocks leads to water compositions very different from those observed both in the north and south. In addition to hydrothermal alteration and deep emanations, the Cl/Br ratio reveals a major contribution of saline waters to the two groups: infiltrating brines from salt lakes in the north; seawater in the south.In the north, concentrations of Cl, Br, Na, K, Ca, SO4, Li, B, Si result from the mixing of alteration waters with recycled brines. Hydrothermal alteration is obscured by this massive saline input, except for Mg. δ34S values are consistent with an origin of sulfate from salar brines, which are themselves derived from deep Tertiary gypsum. In the south, two processes account for the composition of thermal waters: mixing of alteration waters with seawater and deep magmatic contribution. The mixing process controls the concentration of Cl, Br, Na, Alk, Si, K, Ca, Mg. Magmatic inputs are detectable for SO4, Li and B. δ34S suggests that sulfate stems from the mixing of alteration waters with either marine SO4 in coastal waters or with deep SO2 in inland waters. In both the north and south, the Mg concentration is drastically lowered (<1 μmol/L) by the probable formation of a chlorite-type mineral. In the south, very small amounts of seawater (<1% in volume) are sufficient to imprint a clear signature on thermal waters. Not only coastal springs are affected by seawater mixing, but also remote inland springs, as far as 150 km from the sea. Subduction of marine sediments in the accretive margin could be the source of the marine imprint in thermal waters of southern Chile. Seawater may be expelled from the subducted lithosphere and incorporated into the mantle source.  相似文献   

7.
Highly mineralized, largely sodium-chloride type, brines in deep artesian basins are similar in composition to the mineralized abyssal hydrothermal waters of present day volcanic regions as well as the material impounded in liquid inclusions of minerals. It is also well established that present brines are very similar to hydrothermal ore-forming solutions. Some highly concentrated brines can be explained by derivation from salt basins but there is no adequate explanation for the worldwide distribution of concentrated brines. Exchange reactions merely change composition, not concentration. Some hydrocarbons found in minerals as well as in brines have originated from CO2, H2O, and H2 liberated from volcanoes and magma chambers. The abyssal brines may be the product of magmatogenic hydrothermal activity or the brines themselves may be the source of ore-forming hydrothermal solutions. If the latter is true, there is still no explanation of the high mineralization of brines. Many brines are deafly similar to sea water but the salts in sea water are largely produced by volcanic activity. It is suggested that many of the brines are formed in deep unexposed parts of artesian basins from highly concentrated hydrothermal solutions migrating from magmatic chambers. --J. A. Redden.  相似文献   

8.
Twenty-four brine samples from the Heletz-Kokhav oilfield, Israel, have been analyzed for chemical composition and Li isotope ratios. The chemical composition of the brines, together with geological evidence, suggests derivation from (Messinian) seawater by evaporation that proceeded well into the gypsum stability field but failed to reach the stage of halite crystallization. The present salinity of the samples (18-47 g Cl/L) was achieved by dilution of the original evaporitic brine by local fresh waters. Like brines from other sedimentary basins, the Li/Cl ratios in the Heletz-Kokhav samples show a prominent Li enrichment (five-fold to eight-fold) relative to modern seawater. The isotopic ratios of Li, expressed in the δ 6Li notation, vary from −26.3 to −17.9‰, all values being significantly higher than that of modern seawater (−32‰) irrespective of their corresponding Li concentration (1.0-2.3 mg/L). The isotopic composition of Li and the Li/Cl ratio in the oilfield brines were acquired in two stages: (a) The original evaporated seawater gained isotopically light Li during the diagenetic interaction between the interstitial Messinian brine and the basin sediments. A parent brine with an elevated Li/Cl ratio was formed. The brine was later diluted in the oilfields. (b) The δ 6Li values of the final brines were determined during epigenetic interaction with the Heletz-Kokhav aquifer rocks. At the same time, the Li/Cl ratio inherited from stage (a) remained largely unchanged. This work represents the first use of lithium isotopic composition to elucidate the origin and evolution of formation waters in sedimentary basins.  相似文献   

9.
The Cretaceous–Paleocene Andean basin system of central-western South America, comprises northwestern Argentina and southwestern Bolivia. It is situated between 62°–68°W and 18°–27°S, but extends westward to northern Chile and northward to Bolivia and Peru. These basins have been interpreted as an aborted foreland rift. In a general sense, it may be possible to relate this rift to the opening of the South Atlantic Ocean, however it was directly associated, in a backarc position, with the subduction of the Nazca Plate below the South American Plate. Three main magmatic episodes were recognized: the pre-rift stage (130–120 Ma) which is characterized by an early phase of anorogenic plutonism, with subalkaline and alkaline granitic intrusives; the syn-rift volcanic episode which started with a mainly alkaline volcanic activity (110–100) in which alkaline rocks prevail; a second more voluminous volcanic episode (80–75 Ma) which is characterized by an alkaline suite represented by basanites and tephriphonolites; and the last volcanic episode (65–60 Ma) which consists of lamproitic sills and basic K rich lava flows. Petrography, chemistry and chronology of the Cretaceous plutonic bodies indicate anorogenic pre-rift related A-type granite complexes closely related to the further evolution of the Cretaceous rift basin. The petrology and geochemistry of the Cretaceous volcanic rocks show strong alkaline affinities and suggest a similar rift-related origin. The geochemical and isotopic characteristics of the alkaline basalts suggest that they originated through low degrees of partial melting of a depleted mantle subcontinental lithosphere which was previously enriched by processes such as the introduction of veins rich in amphibole, high Ti phlogopite, and apatite. Cretaceous plutonic and volcanic rocks from central-southwestern South America are related to an intracontinental rift environment and although their ages are correlative with those of the Paraná volcanic province, their petrology, geochemistry and isotopic compositions reveal different source regions and petrogenetic processes.  相似文献   

10.
《China Geology》2018,1(1):72-83
With the technological development of exploitation and separation, the primary sources of lithium have gradually changed from ore to brine, which has become the main raw material, accounting for more than 80% of the total production. Resources of lithium-bearing brine are abundant in China. This paper has summarized the spatial and temporal distribution, characteristics, and formation mechanism of the lithium-rich brine in China, aiming to provide a comprehensive set of guidelines for future lithium exploitation from brines. Lithium-rich brines usually exist in modern saline lakes and deep underground sedimentary rocks as subsurface brines. The metallogenic epoch of China’s lithium-rich brine spans from the Triassic to the Quaternary, and these brines exhibit obvious regional distribution characteristics. Modern lithium-rich saline lakes are predominately located in the Qinghai-Tibet Plateau. In comparison, the subsurface lithium-rich brines are mainly distributed in the sedimentary basins of Sichuan, Hubei, Jiangxi provinces and so on in south Block of China, and some are in the western part of the Qaidam Basin in Qinghai province in northwestern China. Lithium-rich saline lakes are belonging to chloride-enriched, sulfate-enriched, and carbonate-enriched, while the deep lithium-rich brines are mainly chloride-enriched in classification. On the whole, the value of Mg/Li in deep brine is generally lower than that of brine in saline lakes. The genesis of lithium-rich brines in China is not uniform, generally there are two processes, which are respectively suitable for salt lakes and deep brine.  相似文献   

11.
The Ca–Mg relationship in groundwaters strongly points to the overall dolomitization and local albitization. The Mg/Ca ratios reveal two trends by which saline waters develop: increase of Mg/Ca ratio by evaporation and decreasing Mg/Ca ratios due to dolomitization and albitization. Br/Cl vs. Na/Cl ratios demonstrate that albitization does not play a major role which leaves dolomitization to be the main source for decreasing Mg/Ca ratios in saline waters. In the eastern and southern Region of Lake Kinneret, salinization occurs by mixing with a Ca/Mg molar ratio <1 brine (Ha’On type). Along the western shoreline of the Lake, a Ca/Mg > 1 dominates, which developed by the albitization of plagioclase in abundant mafic volcanics and the dolomitization of limestones. The most saline groundwater of the Tabgha-, Fuliya-, and Tiberias clusters could be regional derivatives of at least two mother brines: in diluted form one is represented by Ha’On water, the other is a Na-rich brine of the Zemah type. Additionally, a deep-seated Ca-dominant brine may ascend along the fractures on the western side of Lake Kinneret, which is absent on the eastern side. Groundwaters of the Lower Jordan Valley are chemically different on both sides of the Jordan River, indicating that the exchange of water is insignificant. All saline waters from the Dead Sea and its surroundings represent a complex mixture of brines, and precipitation and local dissolution of halite and gypsum. Many wells of the Arava/Araba Valley pump groundwater from the Upper Cretaceous limestone aquifer, the origin of the water is actually from the Lower Cretaceous Kurnub Group sandstones. Groundwater drawn from the Quaternary alluvial fill either originates from Kurnub Group sandstones (Eilat 108, Yaalon 117) or from altered limestones of the Judea Group. The origin of these waters is from floods flowing through wadis incised into calcareous formations of the Judea Group. On the other hand, as a result of step-faulting, hydraulic contact is locally established between the Kurnub- and the Judea Groups aquifers facilitating the inter-aquifer flow of the confined Kurnub paleowater into the karstic formations of the Judea Group. Two periods of Neogene brine formation are considered: the post-Messinan inland lagoon resulting in drying up of the Sdom Sea and the evaporation of the Pleistocene Samra Lake, which went further through the stage of Lake Lisan to the present Dead Sea. For the first period, major element hydrochemistry suggests that the saline waters and brines in the Jordan-Dead Sea–Arava Valley transform evolved from the gradual evaporation of an accumulating mixture of sea-, ground-, and surface water. Due to the precipitation of carbonates, gypsum, and halite, such an evaporating primary water body was strongly enriched in Mg, Br, and B and shows high molar ratios of Br/Cl, B/Cl, and Mg/Ca but low Na/Cl ratios. The development of the Br/Cl ratio is chemically modelled, showing that indeed brine development is explicable that way. Along with the evaporation brine, evaporites formed which are leached by infiltrating fresh water yielding secondary brines with Na/Cl ratios of 1. When primary brines infiltrated the sub-surface, they were subjected to Mg–Ca exchange in limestones (dolomitization) and to chloritization and albitization in basic igneous rocks turning them into Ca-Cl brines. These tertiary brines are omnipresent in the Rift. The brines of the late Lisan and Dead Sea were generated by evaporating drainage waters, which leached halite, gypsum, and carbonates from the soil and from the sub-surface. All these brines are still being flushed out by meteoric water, resulting in saline groundwaters. This flushing is regionally enhanced by intensive groundwater exploitation. In variable proportions, the Neogene and late Lisan Lake and Recent Dead Sea brines have to be considered as the most serious sources of salinization of groundwaters in the Rift. Deep-seated pre-Sdom brines cannot strictly be excluded, but if active they play a negligible role only. An erratum to this article can be found at  相似文献   

12.
Analcime (NaAlSi2O6.H2O) forms a characteristic authigenic phase in Andean alluvium of northern Chile. Three stratigraphic units ranging from the lower Cretaceous to the Miocene were studied in order to investigate the presence of analcime in diagenetic assemblages of different ages. The units were deposited in forearc, foreland/back-arc, and intra-arc basinal settings. Characteristics of other sedimentary analcime occurrences were examined in order to define conditions favourable for analcime precipitation. Zeolite zonation and evidence for the original presence of volcanic glass, common to many sedimentary analcime occurrences, are absent in the studied units. Analcime precipitation requires a high Na+/H+ ratio, relatively low Si4+/Al3+ activity and low H2O activity. Diagenetic examination of the three stratigraphic units revealed early quartz and feldspar overgrowths, mechanical clay infiltration, and dissolution of labile rock and mineral fragments, particularly intermediate plagioclase (An30–80). Conditions for these processes are favoured by oxidizing groundwater at near neutral pH. Later diagenesis involved the precipitation of analcime, non-ferroan calcite, quartz, and authigenic clays as the main cementing phases. These formed due to the concentration of oxidizing groundwater and resulted from its continued reaction with detrital feldspars and rock fragments of andesitic and dacitic composition. Analcime precipitation in Andean alluvium resulted from the evolution of saline, alkaline brines under an arid, evaporative climate in closed hydrographic basins with circulating groundwater systems.  相似文献   

13.
周洁  姚仲友  赵晓丹 《地质通报》2017,36(12):2208-2212
在中安第斯高原,包括玻利维亚西部、智利东部、阿根廷北部分布众多的盐湖,湖中含丰富的B、K、Li、Mg和其他蒸发盐类物质,封闭的盆地因蒸发作用使残留盐水中的成矿元素聚集并沉淀。这些矿床的形成与安第斯山的隆起和气侯变化关系密切。通过对该区蒸发岩型矿床的分布特征及成矿特征进行研究,讨论其形成的构造背景,分析成矿要素和找矿方向。  相似文献   

14.
华南陆块液体钾、锂资源的区域成矿背景与成矿作用初探   总被引：7，自引：1，他引：6  
中国华南陆块江汉盆地的江陵凹陷和潜江凹陷以及江西吉泰盆地等裂谷盆地,在白垩纪—古近纪时期,发育了大量的蒸发岩,并形成了富含钾、锂、铷、铯、溴、碘、硼元素的卤水,这些高价值元素的含量多达到工业利用品位或综合利用品位,资源潜力巨大。这些资源的富集区域分布于华南陆块与新华夏裂谷构造的交汇处,同时也是华南花岗岩省与新华夏裂谷玄武岩的分布区。通过对该区域大地构造、火成岩、古气候、古地理特征与全球海侵事件等综合分析,同时结合盆地卤水化学成分的研究,作者提出华南陆块(地区)的中生代—新生代盆地(群)可能是液体钾、锂、铷、铯、溴、碘、硼资源的成矿区;成矿物质受到白垩纪—古近纪火山活动带来的深部物质及海侵事件带来的海水等多源补给,前者主要带来锂、钾、铷、铯等,后者带来钾及溴、碘等。华南盆地卤水中钾、锂等元素的富集是内生与外生地质动力作用的结果,即构造-火成岩-海侵-干旱气候耦合作用的结果,成矿作用过程可以归结为裂谷沉积成矿,主要形成富钾、锂卤水;埋藏阶段这些卤水通常转移到孔隙发育的碎屑岩、玄武岩及断裂带内保存,形成盆地深层卤水矿床。  相似文献   

15.
New data on the geochemistry and isotopic composition of chloride brines of the Siberian Platform are presented. The distribution of stable isotopes (2H, 18O, and 37Cl) in brines of the Tunguska, Angara-Lena, western part of the Yakutian and Olenek artesian basins and 87Sr/86Sr in brines of the western part of the Olenek artesian basin was studied in the context of the problem of genesis of highly mineralized groundwaters. Results of the study and comparative analysis of the geochemical and isotopic peculiarities of the Siberian Platform brines conform to the theory of brine formation through the interaction of connate waters with enclosing rocks.  相似文献   

16.
The aim of this paper is to present a summary of current knowledge about Quaternary climatic changes, sea level fluctuations, tectonic deformation, and volcanic activity in Chile. In the Andean highlands of the hyperarid desert, glaciers and lakes fluctuated repeatedly. Evidence of pluvial periods is not well documented in the marginal desert. On the contrary, pronounced climatic changes are recorded in semiarid Chile. In central Chile two or three major glacial advances have been identified, but they remained confined within the high Cordillera. In the longitudinal valley of the Lake Region geomorphic remnants of four glaciations have been described; 14C dates are available for the last glaciation. The glacial history of the Fjord Region is still obscure. Whether Pleistocene climatic changes in the northern and southern part of Chile were synchronous or not is a problem which requires further investigation. Sea level fluctuations along the Chilean coast are in part ascribed to glacio-eustatic effects. They left striking sets of step-like marine terraces in northern and central Chile. From a paleontologic point of view the Pleistocene corresponds to a pronounced move toward isolation and endemic development of the marine fauna. The Quaternary tectonic tendency seems to be toward extension and not compression expected as sea-floor spreading compensation. Normal faults limiting uplifted, downwarped, and tilted blocks are common. Folds are rarely found. Northern Chile is characterized by an imposing chain of about 600 stratovolcanoes. They rest on Tertiary ignimbrites which cover the altiplano. Quartz-bearing latite-andesites are predominant. Present volcanic activity is sporadic and weak. South of a conspicuous gap between 27 and 33°S, Quaternary volcanism reappears in the high Cordillera, and many volcanoes have erupted violently within historic times. Rocks are fundamentally andesite or basaltic andesite. Poorly sorted ashes including pumice clasts in the Central Valley south of Santiago are interpreted as volcanic mudflows of late Pleistocene age.  相似文献   

17.
沉积盆地深层地下卤水资源量评价之若干探讨   总被引：1，自引：0，他引：1  
沉积盆地深层地下卤水(包括富钾卤水)处于深埋封闭和无补给状态; 卤水具有很高的测压水头, 天然条件下处于停滞状态, 不同储卤构造之间无水力联系; 具有多个平行叠置的储卤层, 不同储卤层之间无水力联系; 储卤层空隙性和渗透性差, 卤水主要富集于背斜、裂隙带和断层裂隙带; 卤水水化学和物理特性在短期内比较稳定; 卤水储存资源量较大, 在开采条件下卤水资源逐渐减少趋于衰竭。本文在分析总结沉积盆地深层地下卤水资源量评价的现状和卤水特征的基础上, 讨论和阐明深层地下卤水资源评价中的若干问题, 包括深层卤水资源量的类型和评价方法的选取、储卤层计算范围和边界的概化处理、渗透性分区和卤水密度影响的处理、测压水头的换算、钻井预测水头降深的确定等, 目的在于提高深层地下卤水资源量评价计算的精度。  相似文献   

18.
I. Zak  J.R. Gat 《Chemical Geology》1975,16(3):179-188
Origin of saline waters in the Shiraz-Sarvistan area, Iran, is determined by a combined isotopic (18O and D) and chemical characterization. Four types are recognized: (a) fresh water of the anticlinal carbonatic aquifer; (b) fresh and brackish runoff in the synclinal basins; (c) salt springs originating through dissolution of rock salt by type (a) fresh water; and (d) residual brines formed in synclinal closed drainage basins, through evaporation of former water types and loss of the relatively less-soluble salts.  相似文献   

19.
古近纪时期,华南江汉盆地的潜江凹陷和江陵凹陷发育盐湖,沉积了巨厚的蒸发岩,并形成和储藏了富锂、钾、铷、铯、溴、碘等元素的卤水资源,这些元素含量达到工业品位或综合利用品位;富锂卤水属于深层地下卤水型锂矿资源,镁锂比值低,是非常优质的锂资源。本文总结了江汉盆地大地构造特征、火成岩及古气候背景,论述了古盐湖沉积岩相特征、富锂卤水水化学、分布及储层特征、卤水中锂的来源与富集机理、卤水型锂矿成矿模式以及富锂卤水勘查与开采技术进展,提出了卤水开发利用中存在的问题和解决途径。江汉盆地富锂卤水成因包括:古盐湖锂可能主要来自高温水岩反应产生的富锂热液流体的补给;在干旱的气候下,古湖水不断蒸发浓缩,导致卤水中锂浓缩富集;在盐湖演化末期,逐渐埋藏的盐类晶间富锂卤水被转移至裂隙、砂岩及玄武岩储层中储集;在较高的地热背景值下,埋藏卤水与储层岩石可能发生水岩反应,进一步促进了卤水中锂的富集。江汉盆地深层卤水初步勘查显示,氯化锂资源量已达到大型工业规模,展示了巨大的资源潜力。此外,卤水锂开采技术已基本形成,建议进一步加强富锂卤水的绿色开发技术研究,制定相关勘查开发规范。  相似文献   

20.
An analysis of the calcium chloride brines and the composition of the host rocks occurring in the Bajocian volcanic formation indicate that these formations represent the parent rocks in which the calcium chloride brines were generated. The original brines were of the sodium chloride type and were altered to calcium chloride as the result of ion exchange between the brine and minerals of the rocks and the process of zeolitization, resulting in concentrated calcium chloride brines. — E.A. Alexandrov.  相似文献   

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