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1.
Etsuo Uchida Takuro Haitani Takayuki Suetsugu Takahiro Kashima Ken Tsutsui 《Resource Geology》2003,53(2):155-161
Abstract. The distribution of Na, K, Ca, Mg, Mn and Fe between the granodiorite JG-la, one of the geochemical standard rocks, and 2M NaCl aqueous solution was experimentally determined at temperatures of 300 to 800C and a pressure of 1 kb using standard cold seal-type pressure vessels. The solid run products melted partially at 800C. Only K shows a significantly different behavior from the experiments using the basalt JB-la (Uchida and Tsutsui, 2000) due to the presence of ortho-clase in the JG-la. The transition elements tend to be preferably partitioned into the aqueous chloride solutions with increasing temperature. At 800C and 1 kb, the Fe concentration of the aqueous chloride solutions reached up to 5,000 ppm, and the Mn concentration up to 350 ppm. The distribution coefficient, KD, i = Ci, sol /Ci , rock, is in the order of Na>K>Mn>Ca> Fe>Mg at 300C, but changed in the order of Mn>N>K>Fe>Ca>Mg at 800C. The distribution coefficients of the divalent cations for the JG-la are higher than those for the JB-1a. The distribution coefficient of the transition elements, Fe and Mn, increases significantly with increasing temperature. The thermodynamic analysis for aqueous speciation revealed that this is attributable to the formation of the tri-chloro complexes of the transition elements at higher temperatures. 相似文献
2.
铁岭市东部山区野生经济植物榛子营养元素地球化学特征 总被引：1，自引：1，他引：0
对辽宁省铁岭市东部山区野生经济植物榛子样品中的常量营养元素P、K、Ca、Na、Mg、S,14种营养微量元素和稀土元素含量进行了分析.结果表明,本区的榛子样品其主量元素化学特征属K > P > Ca型,其中Na元素含量变异系数最大,为44.27.微量元素含量水平均在植物元素含量正常值变化范围内,由高到低,元素含量排列顺序为;Mn > Si > Fe > Zn > B > Cu > Ni > F > Cr > Mo > Co > Se > I > V.其中,V元素变异系数最大,为93.18.稀土元素总量∑REE（平均值）为29.66×10-9,属低含量.元素相关性分析表明,元素K与Na、Mg,S与Mg、Ca,P与K、Na、Mg、Ca,Fe与Mn,Co与Mn,Cu与Zn之间,在0.01水平都表现出极显著的正相关,反映这些元素之间的吸收积累有很好的协同作用. 相似文献
3.
太平洋北部铁锰结核富集区沉积物的元素地球化学特征 总被引：2，自引：1，他引：2
本文对太平洋北部铁锰结核富集区沉积物的元素地球化学作了较为详细的研究。因子分析提供的信息表明,元素的分布主要受三个因子控制:（1）粘土及Fe、Mn氧化物水化物胶体的吸附作用;（2）生物化学作用过程有关的自生沉积作用;（3）海底页岩风化及附近海区的火山喷发作用。元素的来源:（1）Fe、Mn、Cu、Co、Ni、Zn、Cr、Cr、Mg、Al、Ti、K共生,主要来自粘土吸附;（2）C有机、N、Sr、Na及Si、Ca、Sr主要来自生物化学过程沉积;（3）Pb主要来源于岩石碎屑（火山喷发碎屑）。 相似文献
4.
碱尘暴期间松嫩平原西部碱尘气溶胶的主要元素质量浓度排序为Na、Al、Fe、Ca、Mg、K、Ti、Ba、Zn,与当地盐碱化土壤的元素组成吻合,而与沙尘、城市气溶胶的元素组成有差别。风力对碱尘气溶胶元素组成有明显的影响,当风速在8.0~17.1 m/s时,元素组成的质量浓度排序为Na、Ca、Al、Fe、Mg、K、Ba、Ti、Zn。Na元素质量浓度的激增是碱尘暴元素组分的一大特征,明显富集元素为Na和B;相对于当地背景大气气溶胶的富集情况,Zn、Cu、Ba、B的富集因子值在碱尘暴期间明显降低;在各种天气情况下,B、Cu均具有较高的富集因子。碱尘中Ti元素的富集因子值均小于1,而Ca、Fe、K、Mg、Mn、Sr、V的富集因子值为1~4。两个采样点的Ca、Na、Al、Fe、Mg、Ti、Zn的富集因子近似,表明该区碱尘的主要元素具有特定的一致性;而B、Ba、Cu、V的富集因子相差较大,可以作为区分不同碱尘源的标志性元素。 相似文献
5.
Hypogene uytenbogaardtite, acanthite, and native gold parageneses have been revealed at the epithermal Yunoe gold-silver deposit, Magadan Region, Russia. Thermodynamic calculations in the system Si–Al–Mg–Ca–Na–K–Fe–Pb–Zn–Cu–Ag–Au–S–C–Cl–H2O were carried out at 25–400 °C and 1–1000 bars to elucidate the role of hydrothermal solutions in the formation of gold and silver sulfides. Several most probable scenarios for ore-forming processes in the deposit are considered: (1) interaction between cold and heated meteoric waters percolating along cracks from surface to depth and reacting with the host rock—rhyolite; (2) evolution of ascending postmagmatic fluid resulting in chloride–carbonic acid solution, which interacts with rhyolite at 100–400 °C; (3) stepwise cooling of hydrothermal ore-bearing solutions; (4) rapid cooling of ore-bearing hydrotherms on their mixing with cold surface waters. Rhyolite with Pb, Zn, Cu, Cl, S, Ag, and Au clarke contents was taken as an initial host rock. Calculations by model 3 showed the possible formation of uytenbogaardtite and petrovskaite at low-temperature stages. Gold and silver sulfides can be deposited during the mixing of ore-bearing acid chloride–carbonic acid hydrothermal solutions with surface alkaline waters. 相似文献
6.
Fresh mid-ocean ridge basalt glass and diabase have been reacted with seawater at 150–300°C, 500 bar, and water/rock mass ratios of 50, 62, and 125, using experimental apparatus which allowed on-line sampling of solution to monitor reaction progress. These experiments characterize reaction under what we have called “seawater-dominated” conditions of hydrothermal alteration.In an experiment at 300°C, basalt glass undergoing alteration removed nearly all Mg2+ from an amount of seawater 50 times its own mass. In the process, the glass was converted entirely to mixed-layer smectite-chlorite, anhydrite, and minor hematite. Removal of Mg from seawater occurred as a Mg(OH)2 component incorporated into the secondary clay. This produced a precipitous drop in solution pH early in the experiment, accompanied by a dramatic increase in the concentrations of Fe, Mn, and Zn in solution. As Mg removal neared completion and the glass was hydrolyzed, pH rose again and heavy metal concentrations dropped.At water/rock ratios of 62 and 125 and 150–300°C, the mineral assemblage produced was similar to that at a water/rock ratio of 50. Solution chemistry, however, contrasted with the earlier experiment in that Mg concentrations in solution were greater and pH lower. This caused significant leaching of heavy metals. At 300°C nearly all of the Na, Ca, Cu, Zn, and CO2 and most of the K, Ba, Sr, and Mn were leached from the silicates. H2S, Al, Si, and possibly Co were also significantly mobilized, whereas V, Cr, and Ni were not. Little or no seawater sulfate was reduced.Although submarine hot spring solutions sampled to date along mid-ocean ridges clearly come from rock-dominated hydrothermal systems, evidence from ocean floor metabasalts and from heat flow studies indicates that seawater-dominated conditions of alteration prevail at least locally both in axial hightemperature systems and in ridge flank systems at lower temperatures. 相似文献
7.
Mehtap Paul Meryem Seferinoğlu Gul Asiye Ayçık Åke Sandström Michael L. Smith Jan Paul 《International Journal of Mineral Processing》2006
The leaching of coal and coal/asphaltite/wood-ashes in sulfuric acid (pH 1.0, 25 °C, S/L, 1:10) was studied as a function of time; acid consumption and extracted metal concentrations are presented. Whole coals consumed acid rapidly during the first few minutes, followed by slow acid consumption. Wood-, lignite-, and asphaltite-ashes consumed acid in two stages, the rapid phase extending < 30 min and the slow phase extended up to 10 days. The rapid phase was dominated by the dissolution of Ca, K and Mg ions for wood-ash, by Ca, Al and Mg ions for lignite-ash and Ca and Mg ions for asphaltite-ash. The sulfur concentration in solution and the concentrations of Ca, Fe, K, Mg, Na, P, Al and Mn in the aqueous phase verified the neutralizing capacity of the untreated ashes as well as the formation of insoluble sulfates in the residues. The slow phase kinetics differed for different fuels and exhibited leaching of several abundant elements—Fe, Al, K, Na and Mn. Trace elements (Ba, Cd, Co, Cr, Cu, Mo, Ni, Pb, Th, U, V, Zn) sometimes required up to 32 h for maximal extraction from ashes. Suggestions are presented regarding the chemical nature of trace elements in the untreated coals and ashes and suitable residence times for economical industrial processes. We think it possible to combine bacteriological oxidation of sulfidic concentrates of acid leaching from ash of various qualities or even whole coals. 相似文献
8.
Experiments using distilled water, spiked with heavy metal cations and passed through a filtration system composed of greensand
containing 80% glauconite at a rate of 2–4 ml/min, showed: (1) starting fluids containing Cd, Co, Cu, Pb, Mn, Ni, Ag, or Zn
had an average of 90% of the contaminating cation removed from acidic solutions and an average of 84% removed from the basic
solutions; and, (2) filtration through greensand tended to neutralize both acidic and basic solutions. The removal of the
contaminant cation from starting fluids containing K, Na, Ca, Mg, Fe, Si, or Al (the principal constituents of glauconite
plus Ca from shell material) is not as consistently effective as for the first named metals. 相似文献
9.
Ajay Kumar R. K. Singhal Sabyasachi Rout P. M. Ravi 《Environmental Earth Sciences》2013,70(7):3057-3066
The resulting concentration data sets of major (Na, K, Mg, Ca and Fe) and trace elements (Cu, Ni, Co and Mn) in bed and suspended sediments were used to evaluate the enrichment factor for anthropogenic influences and principal component analysis for identifying the origin of source contributions in the studied area. Normalization of metals to Fe indicated that high enrichment factors in the bed sediment were in the order of Co > Cu > Na > Ca > Ni except Mg, K and Mn while for suspended sediments, only Co has a high enrichment factor. High enrichment of Co and Cu reflected the contamination of sediments from anthropogenic sources. The high influence of Na and Ca in sediments may be caused for seawater salinization factor. A significant positive correlation among enrichment factors of various elements of interest suggests a common origin/identical behavior during transport in the sediment system. 相似文献
10.
P. K. Singh Vijay Kumar Singh Pramod Kumar Rajak M. P. Singh A. S. Naik 《Journal of the Geological Society of India》2016,88(2):131-146
In the present investigation all the working lignite seams of Cambay basin of Gujarat have been studied to see the distribution and geochemistry of selected major/minor elements like Fe, Ca, Na, K, Mg, and Mn and trace elements like Cu, Co, Cr, Cd, Ni, Pb and Zn. The vertical variation of these elements along the seam profiles has been studied to see the pattern of distribution of these elements and also to know the horizons of their enrichment and the probable cause. Further, these elements have been correlated among themselves and also with organic and inorganic matter of lignite. The correlation study indicates that in Tadkeshwar upper seam Fe has its affinity with huminite while Mg and Na have their affinity with liptinite and in Tadkeshwar lower seam Na has an affinity with liptinite. In Vastan upper seam Mn and Cu are associated with inertinite and Na with huminite while in Vastan lower seam Cu relates to huminite and Cd to liptinite and huminite. In Rajpardi seam Ca and Co are associated with huminite. The study provides information on the mode of occurrence of elements of less studied lignites of western India. 相似文献
11.
西天山敦德铁矿床磁铁矿原位LA-ICP-MS元素分析及意义 总被引：5，自引：3，他引：2
敦德铁矿床是天山成矿带内新近发现并勘查的一处大型海相火山岩型铁矿床。该矿床的矿石可划分为浸染状、稠密浸染状、条带状和块状4种主要类型。其中的条带状矿石包括磁铁矿_矽卡岩条带和磁铁矿_方解石条带2种亚类型。块状矿石内出现围岩或矽卡岩角砾时则构成角砾状矿石,其磁铁矿的成因无甚差异。根据野外观察和矿相显微研究,认为磁铁矿形成于早期矽卡岩阶段后的退化蚀变阶段,之后又被更晚的硫化物阶段和绿泥石_碳酸盐阶段的矿物叠加。敦德磁铁矿内主要发生了Al、Mn、Mg和Zn的类质同象置换,此外,也含有Ti、Si、Ca等次要元素以及Na、K、V、Cr、Ni、Co等多种可检测到的微量元素。磁铁矿内元素含量在空间上显示出直观的差异,由深部到浅部,Mn、Zn含量升高,Si、Ca、Na、K、Pb、Ba、Sr、Sb、Cu等含量降低。在Ti O2_Al2O3_Mg O图解、Ti O2_Al2O3_(Mg O+Mn O)图解和Ca+Al+Mn_Ti+V图解上,敦德磁铁矿的分析数据均投影于热液交代(矽卡岩)成因区域。综上认为,该矿床的磁铁矿可能为热液充填交代成因。 相似文献
12.
青藏铁路沱沱河取土场草本植物固土力学强度与化学元素含量特征 总被引：3，自引：0，他引：3
以青藏铁路沱沱河取土场草本植物种植区为例, 在野外和室内分别对生长期为5 a的6种草本做了原位拉拔试验、 室内拉伸试验和剪切试验, 分别得到了试验区梭罗草、 碱茅、 冷地早熟禾、 赖草、 垂穗披碱草、 星星草等6种草本根系抗拔力为187.34~57.89 N、 抗拉力为4.44~2.99 N, 抗剪力为4.33~3.85 N. 同时, 对取土场试验区6种草本地上茎叶、 地下根系15种化学元素进行了分析. 结果表明, 地上茎叶和地下根系主要含有Al、 Ca、 Mg、 K、 Fe、 Sr、 Zn、 Mn等8种元素, 其中Al、 Ca、 Mg、 K等4种元素较其余元素含量显著; 此外, 6种草本其根系所含Ca、 Fe、 Zn、 Sr、 Ni、 Cu等6种元素含量均显著大于相应草本种的茎叶部分. 试验区6种草本抗拔力由大至小依次为梭罗草、 赖草、 冷地早熟禾、 垂穗披碱草、 碱茅、 星星草, 6种草本其根系所含的其中前8种主要化学元素依次为Al、 Ca、 Mg、 K、 Fe 、 Zn、 Mn、 Sr等元素, 这说明了取土场试验区6种草本根系固土力学强度与根系所含化学元素具有一定的关系. 相似文献
13.
长江中下游地区地下水中化学元素的背景特征及形成 总被引：46，自引：0，他引：46
本文论证了长江中下游地区地下水中钾、钠、钙、镁、硅、铁、锰、铬、镍、钒、钴、钛、钼、铜、铅、锌、砷、汞、镉、铍、锂、锶、硼、氟、氯、溴、碘的背景特征、形成及分布规律,探讨其与地下水的含水介质成分,上覆岩土性质、氧化还原环境、地下水的径流条件和矿化度以及地下水的酸碱度之间的关系。 相似文献
14.
Basaltic glass and diabase were reacted with seawater at 70°C at 1 bar and 150°C at 500 bars to determine fluid composition and alteration mineralogy. All experiments were performed at a water/ rock mass ratio of 10.The changes in seawater chemistry depended on temperature and crystallinity of the basalt. The experiment at 70°C produced a slight but continuous loss of Mg, Na and K and enrichment of Ca and SiO2 in the seawater while pH decreased slowly. At 150°C, in contrast, Mg and SO4 were quickly and quantitatively removed while Ca, SiO2, Na, K, Fe, Mn and Ba were added to the seawater. pH rose to values between 5.5 and 6.5 after an initial drop to lower values. Basalt glass reacted more extensively at 150°C than diabase.Smectite was the major alteration product (iron-rich saponite) at 150°C for both the glass and diabase experiments. Smectite from the diabase experiment was well crystallized while that from the glass experiment was poorly crystallized. The smectites are similar to smectites found in altered oceanic ophiolitic basalts. 相似文献
15.
16.
《Geochimica et cosmochimica acta》1987,51(9):2241-2253
The carbonate-free metalliferous fraction of thirty-nine sediment samples from four DSDP Leg 92 sites has been analyzed for 12 elements, and a subset of 16 samples analyzed for Pb isotopic composition. The main geochemical features of this component are as follows: i) very high concentrations of Fe and Mn, typically 25–39% and 5–14%, respectively; ii) Al and Ca contents generally less than 2% and 5%, respectively; iii) high Cu (1000–2000 ppm), and Zn and Ni (500–1000 ppm) values; and iv) Co and Pb concentrations of 100–250 ppm. In terms of element partitioning within the metalliferous fraction, amorphous to poorly crystallized oxide-oxyhydroxides removed by the second leach carry virtually all of the Mn, and about 90% of the Ca, Sr and Ni. The well-crystallized goethite-rich material removed by the third leach carries the majority of Fe, Cu, and Pb. These relations hold for sediments as young as ~ 1–2 Ma, indicating early partitioning of hydrothermal Fe and Mn into separate phases.Calculated mass accumulation rates (MAR) for Fe, Mn, Cu, Pb, Zn and Ni in the bulk sediment show the same overall trends at three of the sites, with greatest MAR values near the basement, and a general decrease in MAR values towards the tops of the holes (for sediments deposited above the lysocline). These relations strongly support the concept of a declining hydrothermal contribution of these elements away from a ridge axis. Nevertheless, MAR values for these metals up to ~200 km from the ridge axis are orders of magnitude higher than on abyssal seafloor plains where there is no hydrothermal influence. Mn/Fe ratios throughout the sediment column at two sites indicate that the composition of the hydrothermal precipitates changed during transport through seawater, becoming significantly depleted in Mn beyond 2̃00–300 km from the axis, but maintaining roughly the same proportion of Fe.Most of the Pb isotope data for the Leg 92 metalliferous sediments form approximately linear arrays in the conventional isotopic plots, extending from the middle of the field for mid-ocean ridge basalts toward the field for Mn nodules. The array of data lying between these two end-members is most readily interpreted in terms of simple linear mixing of Pb derived from basaltic and seawater end-member sources. The least radiogenic sediments reflect the average Pb isotope composition of discharging hydrothermal solutions and ocean-ridge basalt at the EPR over the ≈4–8 Ma B.P. interval. Pb in sediments deposited up to 250 km from the axis can be almost entirely of basaltic-hydrothermal origin. Lateral transport of some basaltic Pb by ocean currents appears to extend to distances of at least 1000 km west of the East Pacific Rise. 相似文献
17.
The primary halos of porphyry copper deposits are characterized by compositional zoning in three dimensions. Two ideal zoning patterns can be divided in accordance with the shape of primary halos in space: bell-shaped and anticline-shaped. In the process of alteration-mineralization, K, Si, (OH), Fe, Cu, Mo, Ag, S, Ba, Rb, Pb, Zn, As, etc. were imported, while Na, Ca, Mg, Fe, Al, Ti, Mn, V, Co, Sr, Pb, Zn, etc. were exported or became activated, and then transported and reprecipitated. Both import and export of Fe, Pb and Zn may have taken place. The fundamental factors controlling the zoning of primary halos are: the stability of complexes and the activity of elements; pH, Eh, the behaviour of sulfur and the sulphophile character of elements; the concentration of components and the regularities of isomorphism; temperature and pressure; and tectonic setting and lithological characters of wallrocks. The authors consider that the zoning patterns of primary halos in porphyry copper deposits are the outcome of integrated effects of various factors. 相似文献
18.
作物产量与土壤环境的关系 总被引：11，自引：1，他引：10
作物的产量与土壤元素中Ｎ、Ｐ、Ｋ、Ｎａ、Ｃａ、Ｍｇ、Ｓ、Ｆｅ、Ｍｎ、Ｃｕ、Ｚｎ、Ｂ、Ｍｏ、Ｖ、Ｃｏ、Ｎｉ、Ｃｒ、Ｐｂ、Ｃｄ、Ｈｇ、Ｓｅ、Ｆ、ＴＩ、Ｂａ、Ｔｅ、Ｔａ、Ｓｒ、Ｔｉ、Ｓｉ等元素及稀土、有机质、酸碱度和含水量、含盐量密切有关。 相似文献
19.
Pramod K. Rajak Vijay K. Singh Prakash K. Singh Asha Lata Singh Narendra Kumar Om Prakash Kumar Vishvajeet Singh Aniruddha Kumar 《Environmental Earth Sciences》2018,77(19):698
The Barmer Basin of Rajasthan is significant for its Paleogene lignite sequences. The lignite seam occurs in Akli Formation of Barmer Basin at the depth of 06–241 m. A total of 57 lignite samples were collected from the working faces of lignite mine and were subjected to proximate analysis (moisture, ash yield, volatile matter, and fixed carbon), ultimate analysis (carbon, hydrogen, nitrogen, oxygen and sulfur), elemental analysis (Fe, Ca, Mg, Cd, Mn, K, Na, Cu, Co, Ni, Cr, Zn, and Pb) and rock-eval pyrolysis for mineral carbon (MINC). Some elements like Cu, Cd, Co, Ni, Zn, Pb, Na, and K occur in high concentration, while Mg and Ca have their concentrations lower than World Clarke average. In addition, various minerals and functional groups present in the lignite samples were analyzed through X-ray diffraction and Fourier transform infrared (FTIR) spectroscopy. The mineral (weight and atomic) percentage has also been analyzed through scanning electron microscopy–energy dispersive spectroscopy (SEM–EDS). 相似文献
20.
The objective of this study was to quantify by experiments the initial seawater–suspended basaltic glass interactions following the 1996 outburst flood from the Vatnajökull glacier, Iceland. The altered basaltic glass dissolved in seawater as recorded by the Si release from the glass. The dissolved concentrations of Na, Ca, Si, Ba, Cd, Co, Cu, Hg, Mn, Ni and total dissolved inorganic N increased with time but the concentrations of Mg, K, S, Sr, Fe, Pb and Zn decreased. Calculated 1 to 10 day fluxes for Si range from 38,000 tons/day to 70,000 tons/10 days. The fluxes for other major elements are more uncertain, but the positive flux (release from suspended matter to seawater) of Ca and Na, and negative flux of Mg, K and S are greater than the Si flux. 相似文献