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1.
快离子导体的离子电导率很高(大于1×10-3Ω-1&3183;cm-1),电子电导率很低(小于总电导率的1%)。它的一个重要应用是作固体电池的电解质隔膜。已知的离子导体不下千种,而快离子导体却为数甚少,锂的快离子导体则几乎尚未发现。从研制高能量密度电池的角度考虑,锂的快离子导体是关键材料,这是近几年来对探索锂的快离子导体给予极大重视的原因。在锂型快离子导体中,Li3N是研究得最多的材料,室温下多晶片的离子电导率为6.6×10-4Ω1&3183;cm-1(B.A.Boukamp and R.A.Huggins,1978),但分解电压太低(～0.45V),稳定性差,不可能在电池中应用它。 相似文献
2.
2012年11月-2013年10月,在祁连山中段排露沟流域持续采集1 a的大气降水和出口断面径流样品,对主要可溶离子、pH、电导率EC和总溶解固体TDS进行了分析。结果表明：流域径流与大气降水相比,各项对应离子浓度显著增加,径流TDS均值（255.50 mg·L-1）远大于降水（46.77 mg·L-1）。径流离子类型为Ca2+-Mg2+-HCO3-,呈弱碱性。大气降水离子类型为Ca2+-HCO3-,接近中性。所有径流样品都落在Gibbs分布图的左中端,表明径流离子组成主要受流域岩石风化作用控制。根据Piper图和主要离子的摩尔比值,综合分析得出控制径流离子过程主要是流域碳酸盐岩风化,其次伴随部分硫酸盐和硅酸盐岩石风化。并通过海盐校正分析方法,得出大气降水对出口断面径流主要离子贡献率仅为4.58%。 相似文献
3.
锂是我国关键矿产和高新产业发展的战略性资源之一。贵州铝土矿资源丰富,含铝岩系分布广,勘查发现铝土矿(岩)中伴生大量的锂资源。研究认为,全省含铝岩系中Li含量高,变化范围大(0.55×10-6～2725.03×10-6),平面上Li含量总体呈北东(务正道成矿区)、南西(修文-清镇成矿区)高,中间(播州-瓮安成矿区)低的分布态势;剖面上Li主要富集在矿系上部的致密状铝土岩(矿)中,Li含量一般>500×10-6,矿系中土状铝土矿(岩)Li含量一般<30×10-6;气候温湿、风化及淋滤作用强的陆相湖泊沉积环境,有利于高岭石为主的黏土矿物形成及Li+与Al3+、Mg2+、Fe3+、Fe2+发生类质同象,或被吸附进入黏土矿物层间构造同迁移同富集,Li与Al2O3含量呈正相关关系;成岩成矿后的次生改造阶段,古地磁测量及CIA显示为炎热潮湿的氧化环境... 相似文献
4.
额尔齐斯河源春季水化学及稳定同位素特征研究 总被引：2，自引：0，他引：2
基于2018年4月额尔齐斯河源至富蕴段的河水样品, 综合运用Gibbs图、 Piper三线图、 相关矩阵分析等方法对河水中主要的化学离子、 pH值、 电导率、 TDS和氢、 氧稳定同位素等物理化学指标进行了分析。结果表明： 额尔齐斯河源春季河水呈弱碱性, TDS平均值为72.02 mg·L-1, 整体属于低矿化度水。河水中主要离子浓度序列为HCO3- > SO42- > Ca2+ > Na+ > Cl- > NO3- > Mg2+ > K+, 其中HCO3-、 SO42-和Ca2+是最主要的阴阳离子。水化学类型从库依尔特河的HCO3--Ca2+型转变为额尔齐斯河富蕴段的（HCO3-, SO42-）-Ca2+型。从源区至富蕴段各离子含量整体呈增大趋势, 但其增加过程受到复杂因素的影响而出现差异。河水离子主要受水-岩风化作用控制, 且以碳酸盐岩（石灰岩、 白云岩）为主的风化水解是离子的主要来源, 其次是长石类矿物的风化, 还包括下游人类活动的离子输入等。δD和δ18O沿程逐渐增大, 在下游出现了富集现象。 相似文献
5.
中国第二次北极科学考察沿线气溶胶成分分析 总被引：7，自引：2，他引：5
对2003年7月15~9月28日间中国第二次北极科学考察沿线所采集的气溶胶样品进行分析,获得了Na+、NH4+ 、Ca2+、Cl-、MSA、SO42- 等11种离子的浓度数据(文中使用当量浓度).根据相关分析, 可将11种离子分为3类: 海盐源离子, 包括Na+、Mg2+、K+、Ca2+、Cl-、SO42-; 人为源, 包括NH4+ 、NO3-; 其它源, 包括 CH3COO-、MSA、C2O42-. 气溶胶以海盐气溶胶为主, Cl-、Na+ 离子分别是阴阳离子中含量最大的离子, (Na+ +Cl-)对气溶胶载量(所测定的阴阳离子的总和)的贡献平均为60.2%, 占气溶胶总量的一半以上. NH4+ /SO42- 的比值的平均为0.45, 根据当地的大气环境和气溶胶的离子平衡, 认为气溶胶样品中NH4+ 和 SO42- 主要是以 NH4HSO4的形式结合. 根据考察沿线 NO3- 浓度的变化, 把考察沿线大致分为3个区: 日本海区, 中值为15.2 neq·m-3; 鄂霍次克海及白令海区, 中值为1.8 neq·m-3; 北冰洋区, 其浓度较低, 中值为0.4 neq·m-3. 考察沿线白令海是MSA的高产区. 相似文献
6.
首次报导了秦岭-大别山壳幔岩石高温高压下电导率的测定结果。该区中上地壳主要代表岩石(角闪岩、绢云母石英片岩、千枚岩等)在10-25km的温压条件下,含水矿物出现脱水会引起电导率值升高,认为这是该区出现高导层体的主要原因;中下地壳代表性岩石(片麻岩、麻粒岩、榴辉岩等)由于石英从α相向β相转变,会导致电导率值(σ)下降。在下地壳的温压条件下电导率值一般为10-2到10-3S·m-1;上地幔的代表性岩石由于组成矿物较为基性,电导率值比下地壳高,从0.1到1S·m-1。 相似文献
7.
为了研究青藏高原东北缘老虎沟地区大气颗粒物中水溶性无机离子组分的变化特征,于2016年7月16日至8月11日共采集13个PM2.5样品和4套粒径分级样品。研究结果显示：非沙尘期间,水溶性离子总质量浓度为2.35 μg·m-3,主要离子SO42-、Ca2+、NH4+和NO3-的浓度分别为1.28、0.33、0.32和0.28 μg·m-3,约占水溶性离子浓度总和的94%;沙尘期间,水溶性无机离子总质量浓度为12.63 μg·m-3,是非沙尘期间浓度的5倍,主要离子SO42-、Ca2+、Cl-、Na+和NO3-的浓度依次为5.36、4.77、0.80、0.62和0.61 μg·m-3,约占水溶性离子浓度总和的96%。分级样品分析结果表明,NO3-主要分布在粗颗粒模态,可能是前体物在粉尘表面发生非均相反应产生。在沙尘时期,SO42-主要为粉尘贡献,集中分布在粗颗粒模态。在非沙尘时期,SO42-在粗颗粒模态和积聚模态都有较多的分布。积聚模态的SO42-主要是通过前体物与NH3发生均相反应产生。据估算,非沙尘时期的二次反应对PM2.5中SO42-的贡献约为80%。 相似文献
8.
慕士塔格卡尔塔马克冰川作用区的水文与水化学特征 总被引：9，自引：2，他引：7
利用2003年6月1日~8月25日实测的水文数据,分析了慕士塔格峰卡尔塔马克冰川融水径流的变化特征.卡尔塔马克冰川融水径流主要集中在6~8月,其存在着明显的日变化过程,融水径流受控于温度及降水要素.同时,对8月10~23日采集的冰川径流样品及部分降水样品的pH、EC(电导率)和主要离子(Na+,K+,Ca2+,Mg2+,Cl-,NO3-,SO42-,未检测降水样品的离子含量)的测定结果进行了分析讨论.径流样品略偏碱性,pH和EC呈正相关关系.SO42-和Ca2+是所测离子中主导的阴阳离子.除NO3-外,样品中各离子含量具有一致的变化特征;各离子浓度与流量或水位具有相反的变化趋势.初步讨论了离子的来源,结果表明冰川融水中化学物质组分主要来源于地表. 相似文献
9.
中国首次北极科学考察沿线气溶胶可溶性成分的分析 总被引：6，自引：3，他引：3
中国首次北极科学考察沿线采集的大气气溶胶样品可溶性成分分析表明,大气气溶胶的平均载量为195neq·m-3,Na+和Cl-的贡献为0%,NH4+和SO42-的贡献为27%,nssSO42-对SO42-的贡献为8%.气溶胶中阴、阳离子总量基本相当,大气环境呈中性.气溶胶中可溶性成分具有较强的纬度变化特征.根据离子的变化态势可将离子分为3大类,即1)Na+,Cl-,SO42-,K+,Mg2+,Ca2+;2)NH4+,NO3-;3)MSA.Na+和Cl-具有较好的线性关系,Cl-/Na+的当量浓度比为1.01,小于其在海水中的比值1.1.NH4+和NO3-的浓度随纬度的增加呈现减少的趋势,说明在低纬度近海岸地区人类活动的污染相当强烈.MSA的浓度在白令海区出现高值,与Shemya(52°N,174°E)站夏季浓度1.79±0.83neq·m-3(170±79ng·m-3)相当.通过与不同海区夏季释放DMS的通量对比,进一步证明了低温有利于DMS向MSA的转化. 相似文献
10.
雅鲁藏布江丰水期河水离子组成特征及其控制因素 总被引：1，自引：0，他引：1
为了解雅鲁藏布江丰水期河水离子组成特征及其控制因素,利用2015年采集的8个河水水样,运用数理统计、聚类分析、Piper三线图、Gibbs模型以及离子比值等方法,分析了雅鲁藏布江丰水期河水水化学特征,并探讨了其主要控制因素。结果表明：河水中阳离子以Ca2+、Mg2+为主,阴离子则以HCO3-和SO42-为主,阴、阳离子分别约占其总量的96%和85%。河水水化学类型均为HCO3·SO4-Ca·Mg型。TDS含量介于202.46~371.27 mg·L-1,均值为299.30 mg·L-1,较世界河流平均值高。自上至下,河水水化学特征表现出一定的差异性,河水中主要离子以及TDS、TH、EC的含量沿程表现出下降的趋势,其原因主要有支流河水汇入和降水增加的稀释作用。河水水样均落在Gibbs模型图中部偏左,表明河水中主要离子化学组分主要受水岩作用控制。离子比值法分析表明研究区碳酸盐岩以及蒸发岩的风化溶解是河水水化学的主要控制因素,且存在硅酸盐类矿物的风化。 相似文献
11.
安徽歙县伏川的蛇绿岩套形成于中-晚元古宙,其Nd、Sr和O同位素组成是:εNd(T)=+0.7-+3.8,εSr(T)=+30.7-+53.9,δ18O=3.2-11.0‰。据地质学和同位素地球化学特征,该岩套位于杨子板块南缘、江南古岛弧的弧后小洋盆地轴部。εNd(T)值的变化是由于蛇绿岩形成过程中受到下伏不成熟硅铝质基底地壳的混染引起的;εSr(T)和δ18O的变化,是在蛇绿岩形成时或形成后不久遭受海水热液蚀变的结果。 相似文献
12.
Blue Mountain is a central-type alkali ultrabasic-gabbro ringcomplex (1?1?5 km) introducing Upper Jurassic sediments, Marlborough,New Zealand. The ultrabasic-gabbroic rocks contain lenses ofkaersutite pegmatite and sodic syenite pegmatite and are intrudedby ring dykes of titanaugite-ilmenite gabbro and lamprophyre.The margin of the intrusion is defined by a ring dyke of alkaligabbro. The plutonic rocks are cut by a swarm of hornblende-biotite-richlamprophyre dykes. Thermal metamorphism has converted the sedimentsto a hornfels ranging in grade from the albite-epidote hornfelsfacies to the upper limit of the hornblende hornfels facies. The rocks are nepheline normative and consist of olivine (Fo82-74),endiopside (Ca45Mg48Fe7-Ca36Mg55Fe9), titanaugite (Ca40Mg50Fe10-Ca44Mg39Fe17),plagioclase (An73-18), and ilmenitetitaniferous magnetite, withvarious amounts of titaniferous hornblende and titanbiotite.There is a complete gradation between end-iopside and titanaugitewith the coupled substitution Ry+z+Si(Ti+4+Fe+3)+Al+3 and asympathetic increase in CaAl2SiO6 (0?2-10?2 percent) and CaTiAl2O6(2?1-8?1 per cent) with fractionation. Endiopside shows a small,progressive Mg enrichment along a trend subparallel to the CaMgSi2O6-Mg2Si2O6boundary, and titanaugite is enriched in Ca and Fe+2+Fe+3 withdifferentiation. Oscillatory zoning between endiopside and titanaugiteis common. Exsolved ilmenite needles occur in the most Fe-richtitanaugites. The amphiboles show the trend: titaniferous hornblende(1?0–5?7 per cent TiO2)kaersutite (6?4 per cent TiO2)Fe-richhastingsite (18?0–19?1 per cent FeO as total Fe). Biotiteis high in TiO2 (6?6–7?8 per cent). Ilmenite and titaniferousmagnetite (3?5–10?6 per cent TiO2) are typically homogeneousgrains; their composition can be expressed in terms of R+2RO3:R+2O:R2+3O4. The intrusion of igneous rocks was probably controlled by subterraneanring fracturing. Subsidence of the country rock within the ringfracture provided space for periodic injections of magma froma lower reservoir up the initial ring fracture to form the BlueMountain rocks at a higher level. Downward movement of the floorof the intrusion during crystallization caused inward slumpingof the cumulates which affected the textural, mineralogical,and chemical evolution of the rocks in different parts of theintrusion. The order of mineral fractionation is reflected by the chemicalvariation in the in situ ultrabasic-gabbroic rocks and the successiveintrusions of titanaugite-ilmenite gabbro and lamprophyre ringdykes, marginal alkali gabbro and lamprophyre dyke swarm. Aninitial decrease, then increase in SiO2; a steady decrease inMgO, CaO, Ni, and Cr: an initial increase, then decrease inFeO+Fe2O3, TiO2, MnO, and V; almost linear increase in Al2O3and late stage increase in alkalis and P2O3, implies fractionationof olivine and endiopside, followed by titanaugite and Fe-Tioxides, followed by plagioclase, hornblende, biotite, and apatite.Reversals in the composition of cumulus olivine and endiopsideand Solidification Index, indicate that the ultrabasic-gabbroicsequence is composed of four main injections of magma. The ultrabasic rocks crystallized under conditions of high PH2Oand fairly high, constant PO2; PH2 and PO2 increased duringthe formation of the gabbroic rocks until fracturing of thechamber roof occurred. The abundance of euhedral amphibole inthe latter injection phases suggests that amphibole accumulatedfrom a hydrous SiO2 undersaturated magma when an increase inPO2, stabilized its crystallization. Plutonic complexes similar to Blue Mountain are found withinand beneath the volcanic piles of many oceanic islands, e.g.Canaries, Reunion, and Tahiti, and those intruding thick sedimentarysequences, as at Blue Mountain, e.g. the pipe-like intrusionsof the Monteregian Hills, Quebec. 相似文献
13.
Water solubility in orthopyroxene 总被引：7，自引：0，他引：7
The solubility of water in pure enstatite was measured on samples synthesized at 1,100 °C and pressures to 100 kbar. Enstatite crystals were grown under water-saturated conditions from a stoichiometric mixture of high-purity SiO2 and Mg(OH)2. Water contents were calculated from polarized FTIR spectra measured on oriented single crystals. The water solubility in orthoenstatite increases with pressure to 867ᆷ ppm H2O by weight at 75 kbar. At 100 kbar, in the stability field of high-clinoenstatite, a water solubility of 714ᆷ ppm was observed. The water solubility in enstatite at 1,100 °C can be described by the equation cH2O=AfH2O exp(-P(V/RT), where fH2O is water fugacity, A=0.0204 ppm/bar and (V=12.3 cm3/mol. The infrared spectra of the hydrous enstatite crystals show a sharp, intense band at 3,363 cm-1 and a broad, weaker band at 3,064 cm-1. Both bands are strongly polarized parallel c. Most likely, pairs of protons attached to non-bridging oxygen atoms substitute for Mg2+. In order to investigate the effect of chemical impurities on water solubility in enstatite, an additional series of experiments was carried out with gels doped with Al, B, or Li as starting material. Whereas, the presence of Li and B had no detectable effect on water solubility, the addition of about 1 wt% Al2O3 increased water solubility in enstatite from 199 to 1,100 ppm at 1,100°C and 15 kbar. In the infrared spectra of these aluminous samples, additional bands occur in the range from 3,450 to 3,650 cm-1. Similar bands are also observed in natural, aluminous orthopyroxenes and are most likely caused by protons coupled with Al according to the substitution of Al3++H+ for Si4+. A series of hydrous annealing experiments on a natural, gem-quality aluminous enstatite from Tanzania yielded water solubilities generally consistent with the results from the synthetic model systems. The results presented here imply that pure enstatite has a similar storage capacity for water as olivine; however, aluminous orthopyroxenes in the mantle may dissolve much larger amounts of water comparable with the entire mass of the present hydrosphere. Moreover, the mechanism of aluminum substitution in orthopyroxenes, i.e., the distribution of Al between tetrahedral and octahedral sites, may be a potential probe of water fugacity. 相似文献
14.
Regional Metamorphism of the Waits River Formation, Eastern Vermont: Delineation of a New Type of Giant Metamorphic Hydrothermal System 总被引：4，自引：0，他引：4
Metamorphic isograds and time-integrated fluid fluxes were mappedover the 1500 km2 exposure of the Waits River Formation, easternVermont, south of latitude 4430'N. Isograds based on the appearanceof oligoclase, biotite, and amphibole in metacarbonate rocksdefine elongated metamorphic highs centered on the axes of twolarge antiforms. The highest-grade isograd based on the appearanceof diopside is closely associated spatially with synmetamorphicgranitic plutons. Pressure, calculated from mineral equilibria,was fairly uniform in the area, 7 1.5 kb; calculated temperatureincreases from {small tilde} 480C at the lowest grades in thearea to {small tilde} 575C in the diopside zone. CalculatedXco2f equilibrium metamorphic fluid increases from <0-03at the lowest grades to 0.2 in the amphibole zone and decreasesto 0.07 in the diopside zone. Time-integrated fluid fluxesincrease with increasing metamorphic grade, with the followingmean values for each metamorphic zone (in cm3/cm2): ankerite-oligoclasezone, 1 x 104; biotite zone, 7 x 104; amphibole zone, 2 x 105;diopside zone, 7 x 105. The mapped pattern of time-integrated fluxes delineates twolarge deep-seated ({small tilde} 25-km depth) regional metamorphichydrothermal systems, each centered on one of the major antiforms.Fluid flowed subhorizontally perpendicular to the axis of theantiforms from their low-temperature flanks to their hot axialregions and drove prograde decarbonation reactions as they went.Along the axes of the antiforms fluid flow was further focusedaround synmetamorphic granitic intrusions. In the hot axialregion fluid changed direction and flowed subvertically outof the metamorphic terrane, precipitating quartz veins. Estimatesof the total recharge, based on progress of prograde decarbonationreactions, nearly match estimates of the total discharge, basedon measured quartz vein abundance, (2-10) x 1012 cm3 fluid percm system measured parallel to the axes of the antiforms. Withinthe axial regions fluids had lower XCO2 and rocks record greatertime-integrated fluxes close to the intrusions than at positionsmore than {small tilde} 5 km from them. The differences in bothfluid composition and time-integrated flux can be explainedby mixing close to the intrusions of regional metamorphic fluidsof XCO2/ with fluids from another source with XCO2{small tilde}0 in the approximate volume ratio of 1:2. 相似文献
15.
Tourmaline has been synthesized hydrothermally at 200 MPa between 300 and 700 °C from oxide mixtures with Mg-Al ratios for the end members dravite NaMg3Al6(Si6O18)(BO3)3(OH)3(OH) and Mg-foitite &ding6F;(Mg2Al)Al6 (Si6O18)(BO3)3(OH)3(OH). Six different Na concentrations were investigated to determine the distribution of Na between tourmaline and fluid in the SiO2-saturated system Na2O-MgO-Al2O3-SiO2-B2O3-H2O-HCl. Synthetic tourmaline ranges from X-site vacant (&ding6F;) tourmaline (Mg-foitite) to nearly ideal dravite with Na=0.95 apfu. There are small, but significant, amounts of proton deficiency and negligible tetrahedral Al. Chemical variation is primarily caused by the substitutions Al&ding6F;Mg-1Na-1 and minor AlMg-1H-1. Varying amounts of Na and &ding6F; determine the Mg/Al ratios. Besides tourmaline and quartz, additional Mg-Al phases are chlorite and, at 700 °C, cordierite. Albite is also present at high Na concentrations in the bulk composition. The c dimension of the tourmaline crystals increases with Na in tourmaline. The amount of Na in the X-site depends strongly on the bulk concentration of Na in the system as well as on the temperature. These factors in turn control the phase assemblage and the composition of the fluid phase. For the assemblage tourmaline + quartz + chlorite/cordierite + fluid, a linear relationship exists between Na concentration in the fluid (quenched after the run) and tourmaline with temperature: T °C [ᆭ °C]=(Nafluid/Natur)앾.878-14.692 (r2=0.96). For the assemblage tourmaline + albite + quartz + fluid, it is: T °C [ᆣ °C]=(Nafluid/Natur)욝.813-6.231 (r2=0.95), where Nafluid is the concentration of Na+ in the final fluid (mol/l) and Natur is the number of Na cations in the X-site of tourmaline. The equations are valid in the temperature range of 500-715 °C. Our experiments demonstrate that the occupancy of the X-site in combination with the changing concentrations of Al and Mg can be used to monitor changes in the fluid composition in equilibrium with a growing tourmaline crystal. Currently, this relation can be applied qualitatively to natural tourmaline to explain zoning in Na- and Al/(Al+Mg). 相似文献
16.
珠江流域岩石风化作用消耗大气/土壤CO2量的估算 总被引：2，自引：0，他引：2
以流域的岩性、径流量和水化学分析数据为主要资料,利用基于GIS空间分析的GEM-CO2模型,估算珠江流域陆地岩石风化作用消耗大气/土壤空气中的CO2,评价河流流域的碳汇能力。结果表明,珠江流域因岩石溶蚀和风化作用消耗大气/土壤中的CO2量为252×109 mol·a-1(571×103 mol·km-2·a-1),从岩性分析,碳酸盐岩区大气/土壤CO2消耗量为180×109 mol·a-1(1030×103 mol·km-2·a-1),占总量的71.4%。二级流域以西江流域CO2消耗量最大,占珠江流域总CO2消耗量79.4%,北江、东江分别占总量的13.0%、4.9%。珠江流域大气/土壤CO2消耗量大约为世界大河流域平均值的2.3倍。 相似文献
17.
Klaus-Dieter Grevel Mirko Schoenitz Volker Skrok Alexandra Navrotsky Werner Schreyer 《Contributions to Mineralogy and Petrology》2001,142(3):298-308
The enthalpy of drop-solution in molten 2PbO·B2O3 of synthetic and natural lawsonite, CaAl2(Si2O7)(OH)2·H2O, was measured by high-temperature oxide melt calorimetry. The enthalpy of formation determined for the synthetic material is (fHOxides=-168.7Dž.4 kJ mol-1, or (fH0298=-4,872.5dž.0 kJ mol-1. These values are in reasonable agreement with previously published data, although previous calorimetric work yielded slightly more exothermic data and optimisation methods resulted in slightly less exothermic values. The equilibrium conditions for the dehydration of lawsonite to zoisite, kyanite and quartz/coesite at pressures and temperatures up to 5 GPa and 850 °C were determined by piston cylinder experiments. These results, other recent phase equilibrium data, and new calorimetric and thermophysical data for lawsonite and zoisite, Ca2Al3(SiO4)(Si2O7)O(OH), were used to constrain a mathematical programming analysis of the thermodynamic data for these two minerals in the chemical system CaO-Al2O3-SiO2-H2O (CASH). The following data for lawsonite and zoisite were obtained: (fH0298 (lawsonite)=-4,865.68 kJ mol-1 , S0298 (lawsonite)=229.27 J K-1 mol-1 , (fH0298 (zoisite)=-6,888.99 kJ mol-1 , S0298 (zoisite)=297.71 J K-1 mol-1 . Additionally, a recalculation of the bulk modulus of lawsonite yielded K=120.7 GPa, which is in good agreement with recent experimental work. 相似文献
18.
The chemical content of the Souss unconfined groundwater displays spatial variations in conductivity (between 400 and 6,000 µS cm-1). The chemical tracers (Cl-, SO42-, Sr2+, Br-), which characterize the different components of the groundwater, allowed the determination of the origin of water salinity. Cl- and SO42-, reaching respectively 2,000 and 1,650 mg L-1, display localized salinity anomalies. Br-/Cl- ratio distinguishes marine-influenced impoverished zones versus the oceanic domain. Thus, salinity anomalies can be attributed: (1) downstream, to a currently existing salt-encroachment (with added waste water) and sedimentary palaeosalinity, (2) in the middle-Souss, to High Atlas evaporites and to irrigation water recycling. Sr2+/Ca2+ ratio (evaporites if >1), confirms the evaporitic origin of the anomalies along the right bank of oued Souss. Furthermore, it facilitates the distinction between the different aquifer contributions (Cretaceous, Jurassic and Triassic), and it highlights leakage from deep Turonian limestones in the groundwater recharge system. To the south, recharge is from the Anti Atlas (evaporite-free) waters. Oxygen-18 measurements confirm the groundwater recharge from the High and Anti Atlas as piezometric maps and chemical tracers suggested, plus from leakage from the Turonian and the marine aquifers. 相似文献
19.
20.
K. T. Fehr R. Hochleitner E. Schmidbauer J. Schneider 《Physics and Chemistry of Minerals》2007,34(7):485-494
The electrical conductivity of monocrystalline triphylite, Li(Fe2+,Mn2+)PO4, with the orthorhombic olivine-type structure was measured parallel (∥) to the [010] direction and ∥ [001] (space group Pnma), between ～400 and ～700 K. Electrical measurements on triphylite are of technological interest because LiFePO4 is a promising electrode material for rechargeable Li batteries. Triphylite was examined by electron microprobe, ICP atomic emission spectroscopy, X-ray diffraction, Mössbauer spectroscopy and microscopic analysis. The DC conductivity σDC was determined from AC impedance data (20 Hz–1 MHz) extrapolating to zero frequency. Triphylite shows σDC with activated behavior measured ∥ [010] between ～500 and ～700 K during the first heating up, with activation energy of E A = 1.52 eV; on cooling E A = 0.61 eV was found down to ～400 K and extrapolated σDC (295 K) ～10?9 Ω?1cm?1; ∥ [001] E A = 0.65 eV and extrapolated σDC(295 K) ～10?9 to 10?10 Ω?1cm?1, measured during the second heating cycle. The enhanced AC conductivity relative to σDC at lower temperatures indicates a hopping-type charge transport between localized levels. Conduction during the first heating up is ascribed to ionic Li+ hopping. DC polarization experiments showed conduction after the first heating up to be electronic related to lowered activation energy. Electronic conduction appears to be coupled with the presence of Li+ vacancies and Fe3+, formed by triphylite alteration. For comparison, σDC was measured on the synthetic compound LiMgPO4 with olivine-type structure, where also an activated behavior of σDC with E A ～1.45 eV was observed during heating and cooling due to ionic Li+ conduction; here no oxidation can occur associated with formation of trivalent cations. 相似文献