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1.
The oxidation state of europium as an indicator of oxygen fugacity   总被引：1，自引：0，他引：1  
The distribution of Eu between plagioclase feldspar and magmatic liquid has been determined experimentally for basaltic and andesitic systems as a function of temperature and oxygen fugacity at one atmosphere total pressure. Using the approach of Philpotts the ratios Eu2+Eu3+ in plagioclase and coexisting magmatic liquid have been calculated. These ratios appear to be simply related to oxygen fugacity for the bulk compositions studied here. Using published trace element distribution data for natural rocks oxygen fugacities may be calculated from these experimental results. For terrestrial basalts calculated oxygen fugacities average 10?7 with little dispersion from this value. Andesites average 10?8.1 with considerable dispersion, while dacites and rhyodacites average 10?9.1, also with considerable dispersion. Oxygen fugacities for lunar ferrobasalts cluster tightly around 10?12.7. Data on achondritic meteorites are limited, but calculations indicate oxygen fugacities of two-to-five orders of magnitude lower than lunar ferrobasalts.  相似文献   

2.
The techniques of electron paramagnetic resonance (EPR) were used to measure the concentration ratio of Eu2+ to Eu3+ in quenched silicate liquids as a function of their compositions. The compositional end members were CaAl2Si2O8 and either MSiO3 or M2Si04, M = Mg, (Ca0.5, Mg0.5), and Ca. All of the liquids were quenched from 1650 ± 25°C, 10?6.9±0.6 atm of oxygen, and 10?6.1±0.6 atm total pressure. For a particular choice of M, the ratio of Eu2+ to Eu3+ increased as much as a factor of 24 with increasing atomic ratio (Al + Si)/(O); for a constant value of (Al + Si)/(O), the ratio of Eu2+ to Eu3+ increased in the order Mg > (Ca0.5,Mg0.5) >Ca. In order to interpret the compositional dependence of the redox equilibrium of Eu in a systematic manner, the concept of a solvent coefficient was introduced.  相似文献   

3.
《Chemical Geology》1999,153(1-4):81-91
Cathodoluminescence (CL) investigations of igneous, metamorphic and sedimentary feldspars indicate that rare earth elements (REE)-activated CL in feldspars is more common than previously assumed. Hot-cathode CL microscopy combined with high-resolution spectrometric analysis of CL emission allow to detect some REE below the detection limits of electron microprobe and proton-induced X-ray emission analysis (PIXE) and reveal variations in the REE distribution within single feldspar crystals. Differently luminescing zones can reflect changes during feldspar crystallization and/or element fluctuations during secondary alteration processes which are not discernible using conventional polarizing microscopy. The results of the study document Eu2+, Sm3+, Dy3+, Tb3+, and Nd3+-activated CL in feldspars of different origin. The influence of the crystal field on shape and position of REE luminescence spectra significantly differs for divalent and trivalent REE ions. Whereas Eu2+ shows a broad band emission (∼420 nm) which is influenced by the local crystal field, trivalent ions of the rare earth show narrow emission lines which reflect the transitions between excited state wave functions lying inside closed electronic shells. The positions of these peaks and the characteristic energies are described for the different REE3+.  相似文献   

4.
Tetraethylenepentamine-modified sugarcane bagasse (SCB) was prepared to improve its adsorption capacity and selectivity toward Cu2+. Adsorption performances of the modified sorbent for Cu2+ were studied in batch system. Separation of Cu2+ from Pb2+ by the modified sorbent fixed-bed column were studied under dynamic system with initial molar concentration ratio \(\left( {C_{0}^{\text{Cu}} /C_{0}^{\text{Pb}} } \right)\) ranging from 1:1 to 1:100. The amount of Cu2+ and Pb2+ adsorbed on the saturated column was calculated by the elution curve. Batch experimental results showed that the adsorption capacity of the sorbent for Cu2+ increased from 0.12 to 0.21 mmol g?1 after modification. Dynamic adsorption results showed that the modified SCB had higher adsorption affinity toward Cu2+ than Pb2+. 0.07 mmol g?1 of adsorbed Pb2+ was pushed off by Cu2+ during the competitive adsorption process at \(C_{0}^{\text{Cu}} /C_{0}^{\text{Pb}} = {\text{1:1}}.\) The breakthrough curves and adsorption kinetics of Cu2+ in the column could be fitted well by the Yoon–Nelson and modified Yoon–Nelson model, respectively. According to the elution curve, the amount of Cu2+ adsorbed on the fixed-bed column were 0.16, 0.16 and 0.15 mmol g?1, while that of Pb2+ were 0.0016, 0.0051 and 0.0094 mmol g?1 when \(C_{0}^{\text{Cu}} /C_{0}^{\text{Pb}}\) increased from 1:1 to 1:10 and 1:100. Cu2+ could be selectively adsorbed and separated from Pb2+ by using the modified sorbent fixed-bed column.  相似文献   

5.
The cathodoluminescence (CL) of a variety of alkali feldspars from South Greenland has been examined in an attempt to understand the causes of the CL and its petrological significance. Analytical methods have included CL spectroscopy, secondary ion mass spectrometry (SIMS) and electron paramagnetic resonance (EPR) to correlate the presence of certain CL emissions to the presence of certain trace element and point defects. Where possible, blue and red luminescent fractions of the same rock samples have been separated and analysed separately. Blue CL appears to relate to the presence of electron holes on bridging oxygens, particularly on the Al-O-Al bridge, as determined from EPR studies. No correlation with other proposed activators for blue CL such as Eu2+, Ga3+ or Ti4+ was observed. Some blue luminescent feldspars also have an emission in the infra-red (IR), invisible during normal visible CL petrography. The red and IR CL emissions correspond to features in EPR spectra attributed to Fe3+ and support previous suggestions that Fe3+ is related to this emission. However, our studies indicate that the visible red CL relates specifically to Fe3+ on the T1 site, whereas the equivalent CL from disordered feldspars lies in the IR. The difference between red and IR CL emissions therefore relates to the state of Fe3+ order across the tetrahedral sites. These data allow more meaningful interpretations of CL as a petrographic tool in alkali feldspar-bearing rocks. Received: 5 March 1998 / Accepted: 23 November 1998  相似文献   

6.
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7.
The techniques of electron paramagnetic resonance (EPR) were used to measure the concentration ratio of Eu2+ to Eu3+ in quenched CaMgSi2O6, Ca3Si3O12, and CaAl2Si2O8 liquids as functions of partial pressure of oxygen and temperature. The redox equilibrium of the Eu ions was described by the reaction 4Eu3+ + 202? = 4Eu2+ + O2. The reduction of Eu3+ to Eu2+ was endothermic, and for CaMgSi2O6 and Ca3Al2Si3O12 liquids the mean value of ΔH0 and the standard deviation from that mean were 25 ± 7 kcal/mole.The magnitude of the Eu anomaly in the distribution coefficients is discussed in terms of the compositions of the solid and liquid phases.  相似文献   

8.
再论花岗岩按照Sr-Yb的分类:标志   总被引：41，自引：14，他引：27  
张旗  金惟俊  李承东  王元龙 《岩石学报》2010,26(4):985-1015
2006年作者曾经按照Sr=400×10~(-6)和Yb=2×10~(-6)作为标志将花岗岩分为埃达克岩、喜马拉雅型花岗岩、浙闽型花岗岩和广西型花岗岩,在浙闽型中又分出南岭型(Sr100×10~(-6)和Yb2×10~(-6)),于是花岗岩被分为5类。Sr=400×10~(-6)和Yb=2×10~(-6)是根据阿留申群岛中的Adak岛的资料得出来的。本文统计了全球花岗岩6000多个数据(其中,埃达克型花岗岩为2810个,喜马拉雅型花岗岩636个,浙闽型花岗岩1183个,南岭型花岗岩1518个,广西型花岗岩142个,总共6289个),统计的结果,各类花岗岩的地球化学特征大致如下:(1)埃达克型花岗岩富Al_2O_3和Sr,贫Y和Yb,具较高和变化的铕异常,绝大多数样品的Sr300×10~(-6),Yb2.5×10~(-6)(当Sr=400×10~(-6)～600×10~(-6)时Yb值最大,Sr超过600×10~(-6),Yb降低至2×10~(-6)),Al_2O_3在14%～18%之间,Eu/Eu~*大多在0.6～1.2范围;(2)喜马拉雅型花岗岩贫Sr和Yb,具中等的Al_2O_3和变化的Eu/Eu~*,Sr300×10~(-6)和Yb2×10~(-6)(少数Sr300×10~(-6)),Al_2O_3为13%～17%,Eu/Eu~*为0.2～1.0;(3)浙闽型花岗岩贫Sr富Yb,Sr在40×10~(-6)～400×10~(-6)之间,Yb1.5×10~(-6),Al_2O_3和Eu/Eu~*的变化类似喜马拉雅型花岗岩,Al_2O_3为12%～17%,Eu/Eu~*为0.4～1.0;(4)南岭型花岗岩以很低的Sr、Al_2O_3和Eu/Eu~*以及很高的Yb而不同于上述各类花岗岩,通常Yb1.5×10~(-6),Sr100×10~(-6)(Yb变化大,绝大多数2×10~(-6);当Yb在2×10~(-6)～8×10~(-6)时,部分样品Sr可100×10~(-6),但很少200×10~(-6));Al_2O_314%,集中在11%～13%之间,Eu/Eu~*0.7,大多0.4;Yb越大,Sr越低,负铕异常越明显。文中讨论了花岗岩Sr-Yb分类的意义,指出本分类适用于产于大陆和海洋的绝大多数中酸性岩浆岩(可能不适用于一部分特别富铁和钾的花岗岩,如具有高Sr和Yb特征的广西型花岗岩)。不同类型的花岗岩主要反映了源区压力的不同,而源区成分、温度、部分熔融程度、水和挥发分的加入以及岩浆混合等的影响可能是次要的。文中指出,该分类的依据、其实质,是熔体与残留相平衡的理论。与浙闽型花岗岩平衡的残留相是斜长石,与喜马拉雅型花岗岩平衡的是斜长石+石榴石,与埃达克型花岗岩平衡的是石榴石,与南岭型花岗岩平衡的是富钙的斜长石。文中指出,加强实验岩石学研究,将年代学和地球化学研究密切结合起来是深化花岗岩研究的关键。  相似文献   

9.
Electron paramagnetic resonance (EPR) measurements were made on Gd3+ and Eu2+ ions in polycrystalline samples to determine the nature of the sites occupied by those ions in mineral structures. Both Gd3+ and Eu2+ ions were incorporated at Ca2+ structural sites in β-Ca2SiO4, pseudo-CaSiO3, CaMgSiO4, CaMgSi2O6, hex-CaAl2Si2O8, CaAl2O4, and Ca3Al2O6. For tri-CaAl2Si2O8, Eu2+ was incorporated at a Ca2+ site and Gd3+ was incorporated at a site where the crystalline electric field was disordered. That difference in behavior may contribute to the anomalous behavior of Eu in plagioclase feldspar. Both Gd3+ and Eu2+ were incorporated as aggregates or clusters of those ions in Mg2SiO4 and clino-MgSiO3.  相似文献   

10.
Plagioclase-melt partition coefficients (D) for 34 trace elements at natural concentration levels were determined experimentally in a natural MORB composition at atmospheric pressure using thin Pt-wire loops. Experiments were carried out at three temperatures (1,220, 1,200, and 1,180°C), and at three different oxygen fugacities (fO2 = IW, QFM, air) in order to assess the effect of fO2 on the partitioning of elements with multiple valence (Fe, Eu, Cr). Run products were analyzed by laser-ablation ICP-MS. Most trace element Ds increase slightly as temperature decreases, except for D Zr, D Fe, D Eu and D Cr that vary systematically with fO2. Applying the Lattice Strain Model to our data suggests the presence of Fe2+ entirely in the octahedral site at highly to moderate reducing conditions, while Fe3+ was assigned wholly to the tetrahedral site of the plagioclase structure. Furthermore, we provide a new quantitative framework for understanding the partitioning behaviour of Eu, which occurs as both 2+ and 3+ cations, depending on fO2and confirm the greater compatibility of Eu2+, which has an ionic radius similar to Sr, relative to Eu3+ in plagioclase and the higher Eu2+/ Eu3+ under reducing conditions. For petrogenetic basaltic processes, a combined fractionation of Eu2+–Sr and Fe–Mg by plagioclase has considerable potential as an oxybarometer for natural magmatic rocks.  相似文献   

11.
Natural fluorite emitting yellow fluorescence under UV light   总被引：1，自引：0，他引：1  
Many mineralogists believe that fluorite emits violet fluorescence under UV light, but a special fluorite from Japan emits yellow fluorescence under UV light. The analysis by inductively coupled plasma-mass spectrometry (ICP-MS) shows that this fluorite includes high concentrations of Dy together with various rare-earth (RE) impurities other than Pm and Eu. Photoluminescence (PL) emission and excitation spectra of the fluorite are investigated at 10, 80 and 300 K. The origin of yellow fluorescence is attributed to the electronic transition within Dy3+. Profiles of the PL and excitation spectra depend on the excitation wavelength and on the observation wavelength, respectively. The obtained spectra are ascribed to the RE ions Ce3+, Sm3+, Tb3+, Dy3+, Ho3+, Er3+, Sm2+ and Yb2+ in the fluorite. In natural fluorite, the low concentration of Eu enables us to observe the bright fluorescence characteristic of trivalent RE ions, instead of the bluish violet fluorescence due to Eu2+.  相似文献   

12.
Shallow groundwater and hot springs were collected from northeastern Guangdong Province, Southeast China, to determine the concentrations and fractionation patterns of rare-earth elements(REE). The results show that the La, Ce and Nd of REEs are abundant in groundwater and rock samples, and the ∑REE contents in groundwater and rock samples range from 126.5 to 2875.3 ng/L, and 79.44 to 385.85 mg/L, respectively. The shallow groundwater has slightly HREE-enriched PAAS-normalized patterns. However, the granitic rocks PAAS-normalized patterns, with remarkable negative Eu anomalies, are different from that of shallow groundwater. The enrichment of HREE is considered to be controlled by REE complexation and readsorption for most groundwater has Ce and Eu positive anomalies. The Ce and Eu anomalies in groundwater are controlled by redox conditions. Moreover, the Fe-contain sediments dissolution and/or the reduction of Fe oxyhydroxides are another factor contributing to Ce anomalies. The Eu anomalies in groundwater are controlled by the preferential mobilization of Eu2+ during water-rock interaction compared to Eu3+.  相似文献   

13.
The western Awulale metallogenic belt in northwestern China hosts a number of small‐ to medium‐sized porphyry Cu deposits that are associated with albite porphyry. The common presence of plagioclase (albite) as phenocrysts and the absence of hydrous minerals (amphibole and biotite) indicate that the water content of albite porphyry is low. Trace‐element compositions of whole rocks and zircon grains from these ore‐bearing porphyries were measured. Zircon grains from albite porphyries exhibit Ce4+/Ce3+ ratios ranging from 7.75 to 95.1, which indicate that these porphyries have a low oxygen fugacity. Trace element compositions of ore‐bearing porphyries exhibit (La/Yb)N ratios ranging from 1.09 to 11.1 and Eu/Eu* ratios ranging from 0.10 to 0.66. These ore‐bearing porphyries have Zr values ranging from 171 to 707 ppm and Hf values ranging from 8.30 to 18.9 ppm. Combining these porphyries with other ore‐bearing porphyries that formed in the Central Asian Orogenic Belt (CAOB) and the Pacific Rim metallogenic belt, we found that the (La/Yb)N and Eu/Eu* ratios of ore‐bearing porphyries in western Awulale are low, while the Zr and Hf values are high. Specifically, REEs can be used to evaluate the degree of differentiation and degree of partial melting, and Zr and Hf can be used to evaluate the redox conditions and water content of magmatic rocks. Our findings indicate that ore‐bearing porphyries in western Awulale have a lower oxygen fugacity, degree of differentiation, and water content than do others in the CAOB and the Pacific Rim metallogenic belt. Compared to those of ore‐bearing porphyries with lower zircon Ce4+/Ce3+ ratios, the (La/Yb)N ratios of ore‐bearing porphyries in our study are low, and the Zr and Hf values are high. This finding indicates that, under reducing conditions, the degree of evolution and water content may have an important influence on the metal abundance in magmas. There is also a clear relationship between (La/Yb)N, Eu/Eu*, Zr, Hf, and the size of the deposits. Large‐ (>4 Mt Cu) and intermediate (1.5–4 Mt Cu)‐sized porphyry Cu deposits are associated with granitic intrusions that have higher (La/Yb)N and Eu/Eu* ratios and lower Zr and Hf values. This finding indicates that, in addition to oxygen fugacity, the degree of evolution and water content are controlling parameters for metal abundance in magmas, especially in low oxygen fugacity porphyry Cu deposits. Such a conclusion may be useful in the exploration for other concealed porphyry Cu deposits.  相似文献   

14.
Partitioning of Eu(III) in calcite, CaCO3, was evaluated with the aim of collecting data on partition coefficients and to enhance understanding of the incorporation mechanisms. This information will aid in the interpretation of geological processes from rare Earth element (REE) data and in the use of Eu(III) as a chemical analogue for the trivalent actinides, particularly Am(III) and Cm(III). Coprecipitation experiments were carried out by the constant addition method at 25°C and PCO2 = 1 atm. Eu(III) was strongly partitioned from the solution into calcite. For dilute solid solutions (XEu < 0.001), Eu partition coefficients were estimated to be 770 ± 290 and found to be independent of calcite precipitation rate in the range of 0.02 to 2.7 nmol mg−1 min−1. This could be explained by the approximately equal values of the Eu partition and adsorption coefficients. Several solid solution models were tested. A vacancy model for Eu2(CO3)3-CaCO3 is consistent with the experimental results and constraints on geometry for Eu fit in the calcite lattice. For low Eu content, vacancy density is independent of Eu concentration in the solid so logarithm of the ion activity product, log (Eu)2(CO32−)3, depends linearly on log XEu2. The fit of the data to such a model is good evidence that Eu(III) is taken up as a true solid solution, not simply by physical trapping. A model using EuOHCO3-CaCO3 is also consistent with the uptake stoichiometry, but EuOH2+ substitution for Ca2+ would be expected to distort the calcite structure more than is compatible with such a high KD. Several other models, including EuNa(CO3)2-CaCO3, were abandoned because their stoichiometric relationships did not fit the experimental data.  相似文献   

15.
The major and trace element characteristics of black shales from the Lower Cretaceous Paja Formation of Colombia are broadly comparable with those of the average upper continental crust. Among the exceptions are marked enrichments in V, Cr, and Ni. These enrichments are associated with high organic carbon contents. CaO and Na2O are strongly depleted, leading to high values for both the Chemical Index of Alteration (77–96) and the Plagioclase Index of Alteration (86–99), which indicates derivation from a stable, intensely weathered felsic source terrane. The REE abundances and patterns vary considerably but can be divided into three main groups according to their characteristics and stratigraphic position. Four samples from the lower part of the Paja Formation (Group 1) are characterized by LREE-enriched chondrite-normalized patterns (average LaN/YbN = 8.41) and significant negative Eu anomalies (average Eu/Eu1 = 0.63). A second group of five samples (Group 2), also from the lower part, have relatively flat REE patterns (average LaN/YbN = 1.84) and only slightly smaller Eu anomalies (average Eu/Eu1 = 0.69). Six samples from the middle and upper parts (Group 3) have highly fractionated patterns (average LaN/YbN = 15.35), resembling those of Group 1, and an identical average Eu/Eu1 of 0.63. The fractionated REE patterns and significant negative Eu anomalies in Groups 1 and 3 are consistent with derivation from an evolved felsic source. The flatter patterns of Group 2 shale and strongly concave MREE-depleted patterns in two additional shales likely were produced during diagenesis, rather than reflecting more mafic detrital inputs. An analysis of a single sandstone suggests diagenetic modification of the REE, because its REE pattern is identical to that of the upper continental crust except for the presence of a significant positive Eu anomaly (Eu/Eu1 = 1.15). Felsic provenance for all samples is suggested by the clustering on the Th/Sc–Zr/Sc and GdN/YbN–Eu/Eu1 diagrams. Averages of unmodified Groups 1 and 3 REE patterns compare well with cratonic sediments from the Roraima Formation in the Guyana Shield, suggesting derivation from a continental source of similar composition. In comparison with modern sediments, the geochemical parameters (K2O/Na2O, LaN/YbN, LaN/SmN, Eu/Eu1, La/Sc, La/Y, Ce/Sc) suggest the Paja Formation was deposited at a passive margin. The Paja shales thus represent highly mature sediments recycled from deeply weathered, older, sedimentary/metasedimentary rocks, possibly in the Guyana Shield, though Na-rich volcanic/granitic rocks may have contributed to some extent.  相似文献   

16.
This paper reports the results of numerical simulation for the behavior of rare earth elements (REE) during decompression degassing of H2O- and Cl-bearing granite melts at pressures decreasing from 3 to 0.5–0.3 kbar under near isothermal conditions (800 ± 25°C). Fluid phase in equilibrium with the melt contains mainly chloride REE complexes, and their behavior during magma degassing is, therefore, intimately related to the behavior of chlorine. It was shown that the contents and distribution patterns of REE in the aqueous chloride fluid phase formed during decompression vary considerably depending on (1) the contents of volatiles (Cl and H2O) in the initial melt, (2) the redox state of the magma, and (3) the dynamics of fluid phase separation from magmas during their ascent toward the Earth’s surface. During decompressiondriven degassing, the contents of both Cl and REE in the fluid decrease, especially dramatically under opensystem conditions. The REE patterns of the fluid phase compared with those of the melt are characterized by a higher degree of light to heavy REE fractionation. A weak negative Eu anomaly may be present in the REE patterns of Cl-rich fluids formed during the early stages of degassing at relatively high pressures. At a further decrease in pressure and Cl content in the fluid, it is transformed into a positive Eu anomaly increasing during decompression degassing. Such an anomalous behavior of Eu during degassing is related to its occurrence in magmatic melts in two valence states, Eu3+ and Eu2+, whereas the other REE occur in melts mainly as (REE)3+. The Eu3+/Eu2+ ratio of melt is controlled by the redox state of the magmatic system. The higher the degree of melt reduction, the more pronounced the anomalous behavior of Eu during decompression degassing. The amount of REE extracted by fluid from melt during various stages of degassing does not significantly influence the content and distribution patterns of REE in the melt.  相似文献   

17.
El Atshan mining area, central Eastern Desert, represents one of the uranium occurrences related to alkaline volcanic rocks in Egypt. Based on the plot of total alkali elements versus silica, these rocks are classified as trachytes. The U and Eu anomalies appear to be derived from trachyte exposed to a long period of alteration and rock–fluid interaction. The trachyte has been subjected to two phases of alteration. The pronounced chemical changes include the mobility of Si, Na, Fe, U, Zn and REE and the immobility of Mg, Th, Hf, Ta and Sc. The late stage hydrothermal solutions caused the breakdown of the feldspars by losing sodium, potassium and partially silica and eventually formation of argillic alteration products, dissolution of iron-bearing sulphides, formation of iron-oxy hydroxides and corrosion of primary uranium minerals forming uranyl oxide hydrates. The acidic water percolating through the fractured trachyte rock leached not only available major or trace elements, but also REE. Eu originally incorporated in feldspars as Eu+2 has been oxidized to Eu+3 and subsequently leached away leaving a negative anomaly in the host rock. The leached U and Eu were then transported most probably as carbonate complexes. The second phase of alteration occurred at the near surface profile when the late stage hydrothermal fluids cool to the temperature of meteoric water and may have mixed with it, the pH of the fluids would shift to more alkaline values and at these conditions U and Eu were precipitated into the fracture system mainly by being adsorbed on the clay minerals and probably coprecipitated with iron oxy-hydroxides.  相似文献   

18.
The 2-site protolysis no electrostatics surface complexation and cation exchange (2SPNE/CE) model used in previous work to model the sorption of Ni and Zn on Na- and Ca-montmorillonites was applied to sorption edges and isotherms measured for Eu on these two montmorillonite forms. The aim was to further test the applicability of the sorption model on a trivalent element with a more complex aqueous chemistry. An additional reason for choosing Eu was that it is considered to be a good chemical analogue for other lanthanides and trivalent actinides. With site types, site capacities, and protolysis constants fixed at the values in the Ni/Zn studies, all of the measured sorption edge data could be modelled using cation exchange and the monodentate surface species, ≡SSOEu2+, ≡SSOEuOH+ and ≡SSOEu(OH)3−, on the strong site type. However, an additional modelling study showed that the same data were almost equally well described by considering bidentate surface complexes, (≡SSO)2Eu+ and (≡SSO)2Eu(OH)2−, and cation exchange. To model the sorption isotherm measurements up to pH = 7.2, only one additional weak site surface complex was required, ≡SW1OEu2+ for the monodentate case and (≡SW1O)2Eu+ for the bidentate case. Selectivity coefficients are given for Eu3+- Ca2+ and Eu3+- Na+ exchange on the planar sites and surface complexation constants for monodentate and bidentate Eu surface species on the edge sites of montmorillonite.  相似文献   

19.
Summary Rare Earth Element (REE) data of 34 samples of magmatic rocks from the Lofoten Islands in Norway lend support to the derivation of anorthosites, ferrodiorites and jotunites by fractionation and cumulus processes from typical basaltic magma. Both REE concentration and Eu anomalies (expressed as Eu/Eu*) form continuous linear trends from anorthosite towards gabbro, ferrodiorite and jotunite in discrimination diagrams against molar CaO/Al2O3 ratios indicating the predominant accumulation of plagioclase. Eu/Eu* decreases from about 4 in the cumulates (anorthosites) to around 1 in the fine-grained gabbroic dikes and to below 1 in some ferrodiorites and the jotunite. The various types of ferrodiorites and the jotunite are regarded as residual liquids, in some cases with variable amounts of cumulus plagioclase. The whole fractionation series from gabbro towards anorthosites and ferrodiorites can be observed in a single intrusion. With increasing fractionation, the REE patterns generally change from flat, slightly LREE-enriched or LREE-depleted to steep and strongly LREE-enriched. These changes and the REE abundances are mainly controlled by the abundance of apatite. Temporally and spatially related mangerites and charnockites form a trend from low-SiO2 mangerites with Eu/Eu* > 1 to intermediate-SiO2 acidic mangerites with Eu/Eu* ≈ 1 and charnockites with Eu/Eu* < 1. Accordingly, the low-SiO2 mangerites are interpreted as alkali feldspar-rich cumulates and the charnockites as residual liquids derived from the acidic mangerites. The mangerites with Eu/Eu* around 1 have patterns similar to those of some highly evolved ferrodiorites possibly indicating a genetic link. Received December 12, 1999; revised version accepted November 15, 2000  相似文献   

20.
Homogenized samples of raw clays resulting from two (2) different lots of natural clays from Maghnia (Algeria) have been assessed for their potential use in the removal of Pb2+ and Zn2+ ions from industrial liquid wastes (LW). Raw and acid-activated samples have been characterized by powder X-ray diffraction, FT-IR spectroscopy, electron microscopy (SEM), and X-ray fluorescence (XRF) and used as adsorbents for the removal of Pb2+ and Zn2+ ions from aqueous system using adsorption method under different conditions. The effect of factors including contact time, pH, and dosage on the adsorption properties of Pb2+ and Zn2+ ions onto clays was investigated at 25 °C. The obtained results revealed that the removal percentages of Pb2+ and Zn2+ ions, from both aqueous solution (AS) and LW, were varying between 90 and 98% for 40 min and optimal pH values ranged from 5 to 6 for Pb2+ and Zn2+ ions, respectively. The kinetics of both Pb2+ and Zn2+ ion adsorption fitted well with the pseudo-second-order model. Langmuir, Freundlich, and Temkin adsorption isotherms were used, and their constants were evaluated. The values of thermodynamic parameters, ΔH°, ΔS°, and ΔG° indicated that the adsorption of Pb2+ and Zn2+ ions was spontaneous and exothermic process in nature. The adsorption and desorption isotherms indicated that Pb2+ and Zn2+ adsorption to raw clays was reversible. The experimental results obtained showed that the raw clays from Maghnia (Algeria) had a great potential for removing Pb2+ and Zn2+ ions from industrial liquid wastes using adsorption method.  相似文献   

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