洛川黄土-红粘土序列铁氧化物组成及其古气候指示   总被引：2，自引：0，他引：2  

谢巧勤  陈天虎  孙玉兵  李晓萱  徐晓春 《矿物学报》2008,28(4)

对洛川黄土、古土壤和红粘土中磁性矿物组成、成因和相关系进行了研究。结果表明:黄土磁性矿物以风尘磁铁矿为主,少量的成土赤铁矿和成土磁赤铁矿;古土壤磁性矿物以成土磁赤铁矿为主,成土赤铁矿次之,少量的风尘磁铁矿和赤铁矿;红粘土磁性矿物以成土赤铁矿为主,风尘磁铁矿和成土磁赤铁矿次之,少量风尘赤铁矿。黄土、古土壤和红粘土磁性矿物组成差异,反映了其形成期不同的古气候特性以及不同气候条件下生物地球化学作用强度的差异。干冷的冰期,黄土弱成土作用形成了以粗颗粒的风尘磁铁矿核 赤铁矿边的磁化率载体。间冰期的温暖湿润的古气候最有利于生物活动,强烈生物活动导致古土壤中大量纳米超细磁赤铁矿/磁铁矿产生,形成以磁赤铁矿为主,风尘磁铁矿核 赤铁矿边为辅的磁化率载体。红粘土成壤期,强降雨强蒸发的长干短湿的高温炎热的古气候使得红粘土化学风化强烈,生物地球化学活动较弱,形成以磁铁矿核 赤铁矿边和磁赤铁矿核 赤铁矿边的磁化率载体。黄土、古土壤和红粘土磁性矿物组成、磁性矿物相关系是其形成期独特的古气候指示。  相似文献   

南黄海陆架中部沉积物反射率光谱的影响因素分析     

王昆山  石学法  程振波  王国庆  葛淑兰 《海洋科学进展》2007,25(1):46-53

利用Minolta CM-2002光谱光度计对南黄海陆架136个短柱样品20~25cm段的沉积物进行了颜色反射率数据测量,通过化学元素、粒度、磁化率等来确定影响沉积物颜色反射率变化的成分和因素,介绍了反射率光谱的一阶导数和因子分析的方法。分析结果表明,南黄海陆架沉积物颜色反射率受控于沉积物中的铁氧化物、有机质以及粘土矿物和钙质生物碎屑含量。主因子F1指示氧化环境,并与陆源物质相关,F2指示弱氧化环境,F3指示弱还原环境,主因子的波长范围分别是405~445 nm和495~595 nm,605~695 nm,445~485 nm。  相似文献   

Laboratory study of the rates and products of the phototransformations of naphthalene adsorbed on samples of titanium dioxide,ferric oxide,muscovite, and fly ash     

Chantal Guillard  Hervé Delprat  Can Hoang-van  Pierre Pichat 《Journal of Atmospheric Chemistry》1993,16(1):47-59

The photodegradation of naphthalene (NPH), chosen as a model of polynuclear aromatic pollutants, has been studied in the presence of a layer of four water-insoluble inorganic solids which can be found in the troposphere (TiO₂, Fe₂O₃, muscovite, and a fly ash sample). Direct photolysis of NPH is negligible at >340 nm. Dark adsorption of NPH on TiO₂ (mainly anatase, nonporous, 50 m² g^–1) at 293 K corresponds to a surface coverage ofca. 50% at equilibrium. Under these conditions (saturated surface), the stationary-state photocatalytic degradation reaches 0.4 molecule nm^–2 h^–1 (>340 nm, radiant fluxca. 22 mW cm^–2). Dioxygen is required and its partial pressure in air is such that the degradation is zero order in O₂. Water vapor markedly increases the rate. The other particulates have also an effect, less important than that of TiO₂, however quite noticeable with respect to surface area unit for the fly ash sample which contains 3.2% Fe₂O₃. Apart from 1,4-naphthoquinone, which is the main intermediate product in all cases, 2-naphthol, phthalide, phthaldialdehyde, phthalic acid, acetophenone, benzaldehyde, benzoic acid are also formed on dry TiO₂. Depending on their volatility, these compounds are transferred to the gas phase or remain principally adsorbed on the solid particles where they are further transformed. For instance, phthalic acid (or anhydride) and benzoic acid are generated from 1,4-naphthoquinone. Degradation mechanisms are briefly discussed.  相似文献   

Iron oxidation state in lower mantle mineral assemblages: II. Inclusions in diamonds from Kankan, Guinea     

C.A McCammon  T Stachel 《Earth and Planetary Science Letters》2004,222(2):423-434

Inclusions of ferropericlase and former (Mg,Fe)(Si,Al)O₃ perovskite in diamonds from Kankan, Guinea believed to originate in the lower mantle were studied using Mössbauer spectroscopy to determine Fe³⁺/ΣFe. Fe³⁺ concentration in the (Mg,Fe)(Si,Al)O₃ inclusion is consistent with empirical relations relating Fe³⁺/ΣFe to Al concentration, supporting the inference that it crystallised in the perovskite structure at lower mantle conditions. In ferropericlase there is a nearly linear variation of trivalent cation abundance with monovalent cation abundance, suggesting a substitution of the form Na_0.5M_0.5³⁺O (M=Fe³⁺, Cr³⁺, Al³⁺). Excess positive charge is likely balanced by cation vacancies, where their abundance is observed to increase with increasing iron concentration, consistent with high-pressure experiments. The abundance of cation vacancies is related to oxygen fugacity, where ferropericlase inclusions from Kankan and São Luiz (Brazil) are inferred to have formed at conditions more oxidising than Fe-(Mg,Fe)O equilibrium, but more reducing than Re-ReO₂ equilibrium. Fe²⁺/Mg partition coefficients between (Mg,Fe)(Si,Al)O₃ and ferropericlase were calculated for inclusions co-existing in the same diamond using Mössbauer data and empirical relations based on high-pressure experimental work. Most values are consistent with high-pressure experiments, suggesting that these inclusions equilibrated at lower mantle conditions. The measured ferropericlase Fe³⁺ concentrations are consistent with diamond formation in a region of redox gradients, possibly arising from the subduction of oxidised material into reduced lower mantle. Reduction of carbonate to form ferropericlase and diamond is consistent with a slight shift of Kankan δ¹³C values to isotopically heavy compositions compared to the worldwide dataset, and could supply the oxygen necessary to satisfy the high Fe³⁺ concentration in (Mg,Fe)(Si,Al)O₃ perovskite, as well as account for the high proportion of ferropericlase in the lower mantle paragenesis. The heterogeneity of lower mantle diamond sources indicates that the composition of lower mantle diamonds do not necessarily reflect those of the bulk mantle.  相似文献   

The importance of iron speciation (Fe+2/Fe+3) in determining mineral assemblages: an example from the high‐grade aluminous metapelites of southeastern Madagascar     

S. D. BOGER  R. W. WHITE  B. SCHULTE 《Journal of Metamorphic Geology》2012,30(9):997-1018

Metapelitic granulites from the Anosyen domain of southeastern Madagascar are exposed in three intercalated formations: the Amparihy, Bakika and Ihosy formations. Although mineralogically distinct from each other, the rocks from these formations show very similar bulk‐rock compositions when measured on a Fe_T basis. The preserved mineral assemblages thus do not reflect differences in the ratios of the main rock‐forming oxides (i.e. Al₂O₃:Fe_T:MgO), but instead reflect variations in the pre‐metamorphic oxidation state of the protolith rocks. These differences in oxidation state are manifested via differences in iron speciation – either Fe⁺² or Fe⁺³. The relatively reduced rocks of the Amparihy Formation preserve the assemblage bi–sp–sill–g–cd, which contrasts markedly with the mostly garnet and spinel‐absent bi–cd–sill–mt assemblages preserved in the strongly oxidized rocks of the Ihosy Formation. Compositionally intermediate rocks of the Bakika Formation are garnet bearing, but sillimanite‐absent, and contain the assemblage sp–g–cd–mag. Modelling of these rocks in the Na₂O–CaO–K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O–TiO₂–O system suggests that they evolved along a heating and cooling P–T path with only limited decompression accompanying cooling on the retrograde path. Peak temperatures and pressures of ～880–920 °C and 6–6.5 kbar are inferred for the majority of the Anosyen domain, with slightly lower peak temperatures (～840 °C) estimated in the extreme northwest of the area. The high‐temperature and relatively low‐pressure nature of metamorphism suggests high geothermal gradients existed during orogenesis, which in southern Madagascar is related to the amalgamation of Gondwana (580–520 Ma). Although metamorphic temperatures may have been augmented via thermal advection from the emplacement of the syn‐ to post‐tectonic Ambalavao suite, the high geothermal gradients nevertheless suggest thin and consequently hot lithosphere existed prior to orogenesis.  相似文献   

由电子探针分析数据估算角闪石、黑云母中的Fe~（3＋）、Fe~（2＋）     

林文蔚  彭丽君 《吉林大学学报(地球科学版)》1994,(2)

待定矿物化学式中阳离子数法是由电子探针分析值求矿物中Ｆｅ￣（３＋）、Ｆｅ￣（２＋）的新方法。在该方法中，矿物化学式中的阴离子数是唯一已知条件，阳离子数未知，通过本文给出的一系列步骤可以得出实际阳离子数的可能估计。进而求出Ｆｅ＿２Ｏ＿２、ＦｅＯ。该法对Ｆｅ＿２Ｏ＿３、ＦｅＯ的计算结果避免了出现负值，在总体上，该方法的计算结果较其它方法更接近其化学分析值。  相似文献   

Application of Chlorite Geothermometry to Hydrothermal Alteration in Toyoha Geothermal System, Southwestern Hokkaido, Japan   总被引：1，自引：0，他引：1  

Atsuyuki Inoue  Kyohei Kurokawa    Tamao Hatta 《Resource Geology》2010,60(1):52-70

In this study, we applied chemical geothermometers to the estimation of formation temperatures of chlorites from various types of hydrothermally altered rocks in the Toyoha geothermal field, using core samples from six drill holes (TH-2 to TH-7) together with wasted ore samples from Toyoha vein-type ore deposit. Based on the preliminary examination of mineral assemblages by X-ray powder diffraction and optical microscopy, hydrothermal alteration observed through the drill holes was classified into four types of alteration zones: propylitic, mixed-layer minerals, kaolin minerals, and ore mineralized zones. The mineral assemblage of the ore mineralized zone observed through TH-2, TH-4, and TH-6 is similar to those of Toyoha ore veins reported previously. The Fe³⁺/ΣFe ratios of chlorites were determined by X-ray photoelectron spectroscopy (XPS), in addition to the usual microprobe analyses. The ratios ranged from 0.20–0.26 for chlorites from the propylitic alteration zone and from 0.13 to 0.17 for those from the ore mineralized zone associated with sulfide minerals. After correcting the Fe³⁺ contents in the octahedral sites of chlorite structures, we obtained acceptable temperatures of the chlorite formation by application of geothermometers, for instance, a similar range of 150–300°C for chlorites from either the propylitic zone or the ore mineralized zone developed through TH-2, TH-4, and TH-6. Chlorites from the ore mineralized zone proximal to the Toyoha deposit are characterized by high Fe and Mn contents compared to the propylitic chlorites, which is similar to the Toyoha vein-filling chlorites; the formation temperatures were close to both the homogenization temperatures of fluid inclusions and the present subsurface temperatures measured through drill holes. Chlorites from the Toyoha ore veins, however, gave slightly higher formation temperatures (180–350°C) than those of chlorites from the ore mineralized zone in the drill cores. This suggests that several types of hydrothermal alteration occurred at different stages in the Toyoha geothermal field and the composition of product chlorite was controlled not only by the temperature but also the composition of fluid related to the formation. Reliable estimation of temperature for the chlorite formation provides basic information on evaluating correctly other physicochemical conditions prevalent at the formation.  相似文献   

载炭泡塑吸附-电感耦合等离子体发射光谱法测定金矿石的金量   总被引：1，自引：1，他引：0  

陈景伟  李玉明  宋双喜  宋江涛  初琳 《岩矿测试》2015,34(3):314-318

载炭泡塑吸附法对金有良好的吸附性能,但只能用于抽滤吸附不能振荡吸附,分析手续繁杂。本文以载炭泡塑振荡吸附-电感耦合等离子体发射光谱法测定金矿石的金量。样品在650℃高温灼烧2 h,用50%王水和10%氯化铁加热溶解,溶液冷却后加入5%高锰酸钾氧化,用中密度规格的载炭泡塑两次振荡吸附溶液中的金,然后于580℃高温灼烧后以50%王水溶解灰分,直接用ICP-OES测定金量。方法检出限(3σ)为0.002μg/g,精密度(RSD,n=11)小于3.7%。本方法对金的吸附率大于99.9%,测定范围为0.01~90μg/g,对不同类型金矿石的适应性强,解决了以往泡塑吸附法吸附率较低、标准系列与样品需同时预处理的问题,对低含量和高含量样品均有较高的准确度。  相似文献   

Estimation of Fe³⁺ from electron microprobe analyses: observations on calcic amphibole and chlorite     

C. E. JACOBSON 《Journal of Metamorphic Geology》1989,7(5):507-513

ABSTRACT Metabasites and metagreywackes from the Pelona and Rand Schists of southern California were analysed using three different electron microprobes. For all three instruments, the estimated Fe³⁺ contents of calcic amphibole, chlorite and epidote are positively correlated. For some samples, there is an additional correlation between high estimated Fe³⁺ and the presence of magnetite. These results imply that microprobe analyses can be used to discern relative differences in Fe³⁺. However, microprobe data and calculations on the sensitivity of the correction procedures to systematic analytical errors indicate that estimated values of Fe³⁺ are not significant in an absolute sense. Thus, estimates of Fe³⁺ are meaningful when comparing samples analysed with a single microprobe, but must be used with caution when comparing analyses obtained on more than one probe.  相似文献   

Influence of ferric iron on phase equilibria in greenschist facies assemblages: the hematite‐rich metasedimentary rocks from the Monti Pisani (Northern Apennines)     

D. Lo Pò  R. Braga 《Journal of Metamorphic Geology》2014,32(4):371-387

We have investigated the effects of different Fe₂O₃ bulk contents on the calculated phase equilibria of low‐T/intermediate‐P metasedimentary rocks. Thermodynamic modelling within the MnO–Na₂O–K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O–TiO₂–O (MnNKFMASHTO) chemical system of chloritoid‐bearing hematite‐rich metasedimentary rocks from the Variscan basement of the Pisani Mountains (Northern Apennines, Italy) fails to reproduce the observed mineral compositions when the bulk Fe₂O₃ is determined through titration. The mismatch between observed and computed mineral compositions and assemblage is resolved by tuning the effective ferric iron content by P–XFe₂O₃ diagrams, obtaining equilibration conditions of 475 °C and 9–10 kbar related to a post‐compressional phase of the Alpine collision. The introduction of ferric iron affects the stability of the main rock‐forming silicates that often yield important thermobaric information. In Fe₂O₃‐rich compositions, garnet‐ and carpholite‐in curves shift towards higher temperatures with respect to the Fe₂O₃‐free systems. The presence of a ferric‐iron oxide (hematite) prevents the formation of biotite in the mineral assemblage even at temperatures approaching 550 °C. The use of P–T–XFe₂O₃ phase diagrams may also provide P–T information in common greenschist facies metasedimentary rocks.  相似文献