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本文以西藏扎布耶盐湖卤水为研究对象，在夏季的大面积盐田中，记录了天然日晒蒸发过程中的卤水组分演化过程，分析了Li、B、K等组分的集散行为，为该湖卤水的综合利用提供了工业化参考数据。通过实验发现，扎布耶盐湖夏季卤水Li^ 富集较低，Li^ 浓度最高达到1.8g/L。Li^ 的析出较分散，在实验末期，固相Li2CO3析出达到高峰期，但Li2CO3的含量不超过4%。在实验后期，卤水中CO3^2-离子的浓度和卤水温度迅速升高，这是导致卤水中Li^ 快速析出的主要因素，蒸发后期，卤水中K^ 和B2O3迅速富集，母卤适于提取硼砂和钾石盐或硼钾盐。 相似文献
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扎布耶盐湖具天然Li2CO3产出，其为微溶矿物，且溶解度随温度升高而降低，其余大多数盐类矿物溶解度均为随温度的升高而升高。不同结构结晶池所产出混盐中Li2O3质量百分数明显不同：露天式为4．06％，MPFS式为2．53％，FPFS式为56．43％。据此，总结出高品位Li2O3混盐制取的基本思路和控制指标：盐田冷冻、日晒，使卤水中Li含量升高至当时水温条件下的饱和点后，不蒸发而升温，卤水中Li饱和后的控制指标为温度。 相似文献
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西藏当雄错盐湖卤水冬季日晒蒸发实验研究 总被引：7，自引：0，他引：7
西藏当雄错盐湖位于藏北高原腹地西南侧,其水化学类型属典型的中度碳酸盐型,具有很好的工业开发前景和价值.自然蒸发是盐田日晒工艺的应用基础工作,本文基于室内卤水等温蒸发实验的相关结果,在当雄错湖区现场开展了盐湖卤水冬季日晒蒸发实验,通过考察碳酸盐型盐湖卤水在现场低温条件下自然蒸发过程中液相各元素的富集规律以及矿物的结晶析盐规律,分析了锂、硼、钾等元素的集散行为,并根据卤水蒸发过程中的元素富集、蒸失水量、盐类析出顺序、矿物组合以及物化性质的变化探索了盐类分离的控制条件.以Na+,K+/CO2-3,SO2-4,Cl--H2O五元体系(25℃)介稳相图为参考依据,绘制了当雄错盐湖卤水冬季日晒蒸发的结晶析盐路线.实验结果表明,当雄错盐湖卤水在冬季日晒蒸发过程中依次析出石盐、泡碱、天然碱、硼砂、钾石盐和扎布耶石,另有少量芒硝和泡碱等低温产物会提前析出或被母液夹带析出,利用冬季低温蒸发可制取富锂卤水,蒸发后期的母卤还可用于提取硼砂和钾石盐等矿物资源.实验结果为下一步开展盐田工程设计及制卤工艺操作提供了必要的基础数据,同时也为碳酸盐型盐湖卤水的综合利用和开发提供了理论支持. 相似文献
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昆特依干盐湖位于柴达木盆地北部,浅部石盐沉积层储存着丰富的地下卤水。研究表明,研究区石盐储层渗透性存在明显的空间分布差异,这种差异对储层中卤水的水化学组成产生显著影响。渗透性较弱的储卤层,卤水赋存于石盐之间的孔隙中,其渗透系数K值为0.01~8.64 m/d,卤水中K+浓度为5.98~10.34 g/L,Mg2+浓度为6.08~13.98 g/L,pH值介于6.8~7.2,SO2-4浓度为19.85~37.93 g/L;说明低渗透性的储卤层具有稳定的水化学环境,且卤水与介质之间基本达到了水-盐作用平衡,应该为早期成盐时圈闭的残余卤水。而渗透性较强的储卤层,K为134.78~198.89 m/d,卤水中K+浓度为2.66~5.60 g/L,Mg2+浓度为4.18~6.24 g/L,pH为7.27~7.44,SO2-4浓度为41.39~61.71 g/L;说明渗透性较强的储卤层,卤水具有较高的SO2-4浓度及pH值和较低的K+、Mg2+浓度,推测由于低盐度水流溶解作用促使储卤层微小孔隙形成大的溶孔,使储层渗透性增强,水体混合导致卤水水化学特性发生改变。 相似文献
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通过测定25℃，50℃，75℃时液相K^ ，Ca^2 ，Mg^2 ，SO4^2-等组成浓度随时间的变化，考察杂卤石在水中的溶解行为，测试得25℃，50℃，75℃条件下杂卤石中K^ 在水中的平衡浓度分别为19．13，21．29，36．77(mg／m1)。K^ 溶解平衡浓度随着温度的升高而增大。实验研究25℃条件下杂卤石在CaCl2溶液中的溶解行为。在5％和10％CaCl2溶液中K^ 的平衡浓度分别为25．65，35．24(mg／m1)。明显大于在水中的平衡浓度。表明CaCl2对杂卤石具有明显的增溶作用，可作为杂卤石的良好溶浸剂。实验结果对不溶性或难溶性的钾矿资源的开发利用具有理论参考和实际应用价值。 相似文献
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高效阴离子交换色谱-紫外检测器联用测定海水中碘 总被引：1，自引：0，他引：1
建立了在碱性体系中采用高效阴离子交换色谱和紫外检测器联用测定海水中碘离子的分析方法。以63mmol／L NaOH为淋洗液，利用IonPac AS16型强亲水性阴离子交换分离柱．碘离子在8．3min洗脱，经抑制器后进入紫外检测器在波长226nm处检测。方法的检出限为0．05μg／L（进样量500μL，3倍信噪比），标准曲线的线性范围为1～2000μg／L（r=0．9995）。20μg／L碘离子标准溶液9次连续进样的相对标准偏差为1．85％。方法已成功地应用于海水中碘离子的测定，1μg／L碘离子的加标回收率为98％～105％。 相似文献
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零价铁去除Cr(Ⅵ)的一系列批实验结果表明：水溶液中发生的氧化还原反应符合准一级反应；对于相同粒度的铁屑(比表面积2．89m^2／g)，固液比由05g／100mL增加到2．0g／100mL，Cr(Ⅵ)质量浓度达到排放标准所需反应时间从26．7min降为3．6min；在固液比相同、原水中Cr(Ⅵ)质量浓度不超过30mg／L时，原水质量浓度增大，达到饮用水标准的反应时间增加；其他条件相同，升高温度可提高零价铁与Cr(Ⅵ)的反应速率。 相似文献
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阴离子交换色谱-电感耦合等离子体质谱联用技术用于面粉中溴形态分析 总被引：1，自引：0，他引：1
建立的阴离子交换色谱-电感耦合等离子体质谱联用技术用于测量面粉中的痕量 BrO3-及Br-。使用DIONEX CarBoPac PA-100(4 mm×250 mm,i．d．)色谱柱,在流速1 mL／min 及5 mmol／L NH4NO3淋洗液下分离BrO3-和Br-。该方法在100μL进样量下BrO3-的检出限为 0．0027 μmoL／L(0．22μg／L),Br-为0．0067 μmoL／L(0．54μg／L)。对市场上部分面粉类样品的分析结果表明,所选面粉只有一种检出有BrO3-,其他样品中的BrO3-均低于检出限。方法的回收率可达到98％-109％。 相似文献
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罗布泊盐湖富钾卤水成因再探讨——碎屑层卤水蒸发实验分析 总被引：1，自引：0，他引：1
罗布泊盐湖钙芒硝岩孔隙中蕴藏有超大型规模的卤水钾矿,富钾卤水成因一直备受关注。罗北凹地从统一的罗布泊大湖区中分隔出来后,成盐过程中其湖水仍以南部大湖的补给为主,罗北凹地卤水化学演化与"大耳朵"湖水密切相关。"大耳朵"湖区含石膏碎屑层普遍储藏有卤水,应该是罗北凹地盐湖的"源卤水",钾离子(ρ(K~+)为3.12 g/L左右)已初步富集,平均矿化度为198.83 g/L。为了查明该卤水的化学演化趋势及析盐序列,笔者于2009年、2010年两次采集了大量卤水样品,分别进行室内等温蒸发和自然蒸发实验。蒸发实验结果表明:随着卤水浓缩首先析出(硬)石膏,随后析出大量石盐,最后出现少量钾石盐和光卤石,与EQL/EVP卤水蒸发模型模拟结果相似。将碎屑层卤水蒸发过程中化学组成变化与罗北凹地卤水进行对比,结果显示罗布泊古湖水蒸发至石膏沉积之后,在罗北凹地水化学组成明显发生变化,没有大量石盐沉积,而以钙芒硝沉积为主。推测应是受到深部"富钙水"的持续补给,而"大耳朵"湖起到"预备盆地"的作用,罗布泊古湖水经"大耳朵"湖蒸发浓缩后,钾离子得到初步富集,在流入罗北凹地后与深部"富钙"水混合,强烈蒸发浓缩,大量钙芒硝矿物析出,最后形成富钾卤水。 相似文献
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盐湖锂资源开发利用及对中国锂产业发展的建议 总被引：10，自引：1，他引：9
近年来,锂及其化合物的用途日益重要而广泛,特别是电动车和各种移动电子设备对大小功率锂电池的需求急剧增长,大大带动了锂资源的开发利用。全球锂资源有80%以上蕴藏在盐湖卤水、油田水、地热水等液体矿床中。在被称为"锂三角"的南美安第斯高原的智利、阿根廷、玻利维亚交界处,分布有丰富的盐湖锂资源,当地少雨、多风、极度干燥的自然条件,对开发盐湖资源十分有利,在当今世界锂开发潮流中,已成为一大热点地区。文章介绍了世界盐湖卤水锂资源的状况和开发利用工艺流程;作为多个新兴产业交汇点的锂产业,从上游锂资源调查评价、加工利用到下游各种产品的研制,近年来在中国都取得了长足发展;最后对中国锂产业的发展提出了一些建议。 相似文献
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Epitaxial salt reefs and mushrooms in the southern Dead Sea 总被引：1，自引：0，他引：1
Salt usually accumulates in shallow ephemeral brines as simple flat beds. However, in permanent brines deepening in solar evaporation ponds in the southern Dead Sea, salt accumulation is complicated by the growth of isolated vegetable-like salt structures and networks of polygonal salt walls. These walls divide large salt ponds, which are easily homogenized by wind, into thousands of small compartments that are less easy to mix. Instead, brines in the compartments stratify when a surficial layer about 10 cm thick supersaturates and floats above the cumulate floors on brines that are merely saturated. Salt reef growth in the southern Dead Sea has previously been attributed to mixing of ions common to brines already in the ponds and those pumped in from the northern basin (with or without subsurface brines rising through the pond floors). A new factor is emphasized here that, whatever the origins of the brines, salt reefs remain emergent by epitaxis, the in situ growth of crystalline substrates already in the surficial supersaturated layer. Epitaxis can be invisible in crystal clear brines and prolongs the obvious crystallization season by replacing sedimentation of grains nucleated and grown on the brine surface as the dominant mechanism of deposition. Salt reefs develop botryoidal overhangs that can merge into salt platforms that roof over deep brines. Salt shallows on the reef platforms and around the pond shores are both characterized by the deposition of the thin flat beds with vertical palisade textures well known from other ephemeral brines. Salt reefs are interpreted as tepee structures which have grown by epitaxis as fast as saturated brines have deepened around them. Epitaxis may also account for the rapid deposition of thick beds of pure salt in rifts that open to oceans. Local histories of salt reef compartmentalization can be read from the shapes of reefs that record their relative rates of growth and drowning. Rather than diminish evaporation area, damp emergent salt reefs act as giant transpirative pumps that accelerate salt crystallization and reconfigure the evaporation ponds into areas smaller than thought necessary by chemical engineers. The natural end of reef formation may be when shallow brines on hollow reef platforms become ephemeral on solid salt flats. Former salt reefs are likely to be distinguishable in the undeformed geological record by their botryoidal layers of nonvertical chevron crystals. 相似文献
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Juske Horita 《Aquatic Geochemistry》2009,15(1-2):43-69
Isotopic fractionations associated with two primary processes (evaporation and freezing of water) are discussed, which are responsible for the formation and evolution of saline lakes in deserts from both low-latitude and the Polar regions. In an evaporative system, atmospheric parameters (humidity and isotopic composition of water vapor) have strong influence on the isotopic behavior of saline lakes, and in a freezing system, salinity build-up largely controls the extent of freezing and associated isotope fractionation. In both systems, salinity has a direct impact on the isotopic evolution of saline lakes. It is proposed that a steady-state “terminal lake” model with short-term hydrologic and environmental perturbations can serve as a useful framework for investigating both evaporative and freezing processes of perennial saline lakes. Through re-assessment of own work and literature data for saline lakes, it was demonstrated that effective uses of the isotope activity compositions of brines and salinity-chemistry data could reveal dynamic changes and evolution in the isotopic compositions of saline lakes in response to hydrologic and environmental changes. The residence time of isotopic water molecules in lakes determines the nature of responses in the isotopic compositions following perturbations in the water and isotope balances (e.g., dilution by inflow, water deficit by increased evaporation, and/or reduction in inflow). The isotopic profiles of some saline lakes from the Polar regions show that they switched the two contrasting modes of operation between evaporative and freezing systems, in response to climate and hydrological changes in the past. 相似文献
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H. Mirnejad V. Sisakht H. Mohammadzadeh A. H. Amini B. J. Rostron G. Haghparast 《Geological Journal》2011,46(1):1-9
Cation and anion concentrations and oxygen and hydrogen isotopic ratios of brines in the Asmari Formation (Oligocene–early Miocene) from the Marun oil field of southwest Iran were measured to identify the origin of these brines (e.g. salt dissolution vs. seawater evaporation) as well as the involvement of water–rock reaction processes in their evolution. Marun brines are characterized by having higher concentrations of calcium (11 000–20 000 mg/L), chlorine (120 000–160 000 mg/L) and bromide (600–1000 mg/L) compared to modern seawater. Samples are also enriched in 18O relative to seawater, fall to the right of the Global Meteoric Water Line and local rain water, and plot close to the halite brine trajectory on the δD versus δ18O diagram. Geochemical characteristics of Marun brines are inconsistent with a meteoric origin, but instead correspond to residual evaporated seawater modified by water–rock interaction, most significantly dolomitization. In addition, anhydrite precipitation or sulphate reduction appears to be important in chemical modification of the Marun brines, as indicated by lower sulphate contents relative to evaporated seawater. Extensive dolomitization, the presence of anhydrite nodules and high salinity fluid inclusions in the upper parts of the Asmari Formation fit a model whereby the Marun brines likely originated from the seepage reflux of concentrated seawater during the deposition of the overlying Gachsaran Formation evaporites in the Miocene. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
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The behavior of lithium and its isotopes in oilfield brines: evidence from the Heletz-Kokhav field, Israel 总被引：2，自引：0，他引：2
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
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卤水中溶解性有机质(dissolved organic matter,DOM)会对盐田日晒工艺和产品质量产生不利影响,如盐田卤水的蒸发速率减缓、蒸发度减小以及提取的矿物产品带有刺鼻的气味、浓重的颜色等。因此,对具有资源开发利用价值的卤水体系中DOM结构和性质的研究可以为后续DOM的有效去除或在DOM共存体系中调控无机盐结晶工艺路线提供有效的指导意见。本文以自然界中广泛存在的两种不同类型的卤水体系,即盐湖卤水DOM(SLDOM)和油田卤水DOM(OFDOM)为研究对象,采用溶解性有机碳(dissolved organic carbon,DOC)分析、光谱学分析和平行因子分析等手段对DOM的含量、分子量分布特征、光谱学结构和光降解行为开展了研究。DOC和荧光分析表明SLDOM和OFDOM的DOC含量和生物指数(BIX)值相似;与OFDOM相比,SLDOM的腐质化指数(HIX)值和高分子量组分(HMW)比例偏高;特别吸收光谱(SUVA254)和糖类化合物含量检测结果表明,SLDOM和OFDOM的HMW组分中含有的芳香类和糖类化合物所占比例比低分子量组分(LMW)高;三维荧光谱图分析(EEM)结果表明,SLDOM主要以腐殖质类物质为主,而OFDOM以蛋白质类组分为主。此外,DOM的荧光组分在不同分子量中的分布也存在明显差异:对于SLDOM,富里酸主要分布在HMW DOM中,而腐殖酸主要在LMW DOM中;对于OFDOM,芳香胺类蛋白组分主要分布在HMW DOM中,色氨酸和酪氨酸类蛋白组分主要分布在LMM DOM中。在光降解实验中,SLDOM和OFDOM的DOC含量随光照时间增加而逐渐减少,分别下降了29.32%和15.11%。进一步的分析表明,光照过程中两种卤水中糖类化合物均减少,小分子量的DOM优先分解。此外,在光照过程中SLDOM芳香类化合物增加,腐质化程度基本不变;OFDOM芳香类化合物减少,腐质化程度增加。EEM平行因子分析(PARAFAC)结果表明,SLDOM荧光组分在光降解过程中荧光强度增加,而OFDOM荧光强度减少。 相似文献
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Effects of the Chemical Compositions of Salars de Uyuni and Atacama Brines on Lithium Concentration during Evaporation 总被引：2，自引：0，他引：2
During Li recovery from salar brines, Li concentration is typically increased to about 60,000 mg L?1 by evaporation. We investigated the concentration changes of Li, Na, K, Mg, Cl, SO4, and B during evaporation of both natural Uyuni and artificial Atacama brines. The Uyuni brine exhibited a maximum Li concentration of 6810 mg L?1 at 31 days of evaporation, at which point the majority of the Na and K in the brine was removed. The Li concentration decreased with further evaporation due to precipitation as Li2SO4, such that the level at the 56 day mark was approximately 4130 mg L?1. In contrast, the artificial Atacama brine showed no pronounced Li precipitation, even after 54 days, at which point the Li concentration was 21,800 mg L?1. The initial concentrations of Na and K in the Atacama brine were higher than those in the Uyuni brine, and the Atacama solution still retained K after 54 days of evaporation. The order of precipitation of cation species during the evaporation of both brines was: Na, followed by K, Mg, and Li. Thus, Li precipitation in the Atacama brine might be prevented due to the more favored precipitations of Na and K, such that significant Li removal did not occur in this brine. 相似文献
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柴达木盆地西北角分布有基岩,盆地西部分布山麓堆积及河、湖相沉积地层,新生界发育有多个北西—南东走向的规模不一的背斜,新近系分布有富钾地下卤水。利用统计方法分析卤水中TDS、K+和B2O3的富集情况。结果显示：TDS值出现双峰,卤水样品富K+和B3+的概率分别为628%和6129%。使用Piper图研究地下卤水时,经常出现样品点过于集中而不易反映主要离子含量的变化。本次研究改进了前人的图示方法,绘制适合于表示地下卤水的水化学图。利用钠氯系数、氯溴系数、氯碘系数、钾氯系数、脱硫系数、钙镁系数对研究区卤水水样进行分析,结果显示卤水样品多数未达到石盐沉积,少数达到石盐沉积。研究区水样氢、氧稳定同位素数据显示新近系地下卤水δ18O值和δD值均发生漂移,表明卤水经历长时间的蒸发浓缩。研究区地下卤水起源于早上新世的古大气降水,上新世以后由于青藏高原快速隆升,柴达木盆地抬升和沉降中心东移,接受沉积形成良好的盖层,同时大气环流的改变致使气候变得干燥,地下卤水经历蒸发浓缩封存,形成现今的卤水。 相似文献