铜川王石凹黑色高岭石粘土岩的成因分析     

柳淑霞  白开寅 《地球科学与环境学报》1996,(1)

黑色高岭石粘土岩，是铜川王石凹煤矿石炭纪煤系地层顶部，五号煤层的上部一层稳定的煤矸石。经偏光显微镜及费氏台测试光性特征、化学试验及分析鉴定表明，这是一种由高岭石组成的，成分很纯、颗粒大、结晶良好的高岭石粘土岩。据微量元素含量分析，此高岭石系淡水沉积物。  相似文献   

氨基酸在粘土高岭石上吸附等温线的研究   总被引：2，自引：0，他引：2  

刘效兰  张正斌 《海洋科学》2002,26(9):1-4

研究了4种氨基酸（甘氨酸，赖氨酸，天冬氨酸，谷氨酸）在粘土高岭石上的吸附等温线以及金属铜离子对其等温线的影响。研究表明，氨基酸在高岭石上的吸附等温线以及金属铜离子存在时的吸附等温线均属Langmuir型等温线；铜离子浓度增加时，其等温线斜率也增加，并认为体系可形成Ⅰ型三元表面络合物，铜离子对氨基酸在高岭石上等温线影响的规律和在相同体系中它对氨基酸在高岭石上交换吸附百分率E（%）-pH曲线的影响规律相一致。  相似文献   

Geochemical evolution of the Capim River kaolin, Northern Brazil     

D.J.L. Sousa  A.F.D.C. Varajo  J. Yvon 《Journal of Geochemical Exploration》2006,88(1-3):329

The Capim River kaolin, located in the eastern Brazilian Amazon, constitutes one of the most important kaolin deposits in the world. Known for its high whiteness, its noble application is in the paper industry. Studies were carried out on samples from the six facies of the deposit (sand kaolin, soft kaolin, lower transition facies, ferruginous crust, upper transition facies and flint kaolin) in order to trace its geochemical evolution. The kaolin developed at the expense of Cretaceous sandy–clayey sediments of the Ipixuna Formation. Intense lateritic processes characterized by ferruginization and deferruginization mechanisms led to the distinction of the different facies.  相似文献   

Incorporation of Cr<Superscript>3+</Superscript> in dickite: a spectroscopic study     

E. Balan  T. Allard  G. Morin  G. Calas 《Physics and Chemistry of Minerals》2002,29(4):273-279

 We have investigated a well-ordered sample of natural Cr-bearing dickite from Nowa Ruda (Lower Silesia, Poland) using electron paramagnetic resonance (EPR) at X- and Q-band frequencies (9.42 and 33.97 GHz, respectively) and optical diffuse reflectance spectroscopy. The observation of the spin-forbidden transitions at 15500 and 14690 cm⁻¹ allows us to unambiguously identify the major contribution of octahedrally coordinated Cr³⁺ ions in the optical spectrum. The X- and Q-band EPR spectra show two superposed Cr³⁺ signals. The corresponding fine-structure parameters were determined at room temperature and 145 K. These results suggest the substitution of Cr³⁺ for Al³⁺ in equal proportions in the two unequivalent octahedral sites of the dickite structure. In kaolin group minerals, the distortion around Cr³⁺ ions (λ≈ 0.2–0.4) in Al sites is significantly less rhombic than that observed around Fe³⁺ ions (λ≈ 0.6–0.8). Received: 29 June 2001 / Accepted: 22 October 2001  相似文献   

Dissolution of well and poorly ordered kaolinites by an aerobic bacterium     

Patricia A. Maurice  Melanie A. Vierkorn  Larry E. Hersman  Julia E. Fulghum 《Chemical Geology》2001,180(1-4):81-97

Previous research by our group (e.g., [Chem. Geol. 132 (1996) 25; Geochim. Cosmochim. Acta 64 (2000) 1363]) has shown that an aerobic Pseudomonas mendocina bacterium enhances Fe(hydr)oxide dissolution in order to obtain Fe under Fe-limited conditions. The P. mendocina is incapable of utilizing Fe as a terminal electron acceptor and requires several orders of magnitude lower Fe concentrations than do dissimilatory Fe reducing bacteria. The research reported here compared the effects of the P. mendocina on dissolution of well and poorly ordered Clay Minerals Society Source Clay kaolinites KGa-1b and KGa-2, respectively, under Fe-limited conditions. KGa-1b and KGa-2 contain 0.04 and 0.94 bulk wt.% Fe, respectively, and their surface Fe/Si atomic RATIOS=0.008 and 0.012. Following strong cleaning of the kaolinites in 5.8 M HCl at 85 °C, the surface Fe/Si atomic ratios decreased to 0.004 and 0.008, respectively. Both kaolinites also developed a Si-enriched surface precipitate upon strong cleaning.

Because the P. mendocina take up Fe, we could not measure Fe release from the kaolinite directly, but rather had to monitor it indirectly by comparing microbial populations sizes under Fe-limited growth conditions. We found that microbial growth on uncleaned, weakly cleaned, and strongly cleaned kaolinites increased with the amount of Fe readily available to organic ligands as estimated by dissolution in 0.001 M oxalate (pH 3). This suggests that it is the amount of readily accessible Fe that controls Fe acquisition and hence microbial growth. The trend is based on only a relatively small range of kaolinite Fe contents, and the research thus needs to be expanded to include kaolinites with a broader range of bulk and surface Fe concentrations.

Significant enhancement of Al release was observed in the presence of the bacteria, along with generally some enhancement of Si release. This enhancement of kaolinite dissolution could be related to an observed pH increase from 7–8 to 9 in the presence of the bacteria and/or to production of Al chelating agents. The P. mendocina produce a variety of organic exudates, including siderophores [Chem. Geol. 132 (1996) 25; Geomicrobiology (2001b)], and further studies into the effects of the siderophores on Al complexation and on kaolinite dissolution are ongoing.  相似文献   

Copper(II) humate mobility in kaolinite soil     

J. Wu  L. J. West  D. I. Stewart   《Engineering Geology》2001,60(1-4):275-284

An investigation of the influence of humate on the mobility of copper(II) ions in a kaolinite soil using leaching tests and electrokinetic experiments is reported. The data are interpreted in terms of humate–copper–clay interactions and humate electrical charge. Humate is mostly immobile below pH8 but is more mobile in alkaline conditions (sorption to kaolinite reduces its mobility in neutral conditions). Copper humate complexes are mobile in both acidic and alkaline conditions, but not in neutral conditions where they are sorbed. The dissolved copper humate complexes that form in acidic conditions are positively charged. The net effect of humate is to increase cupric ion mobility in kaolinite soil, especially in alkaline conditions.  相似文献   

Mineralogy and geochemical behaviour during weathering of greenstone belt under tropical dry conditions in the extreme North Cameroon (Central Africa)     

Jean Pierre Nguetnkam  Fredéric Villiéras  Richard Kamga  Georges Emmanuel Ekodeck  Jacques Yvon 《Chemie der Erde / Geochemistry》2014

Mineralogy, major, trace and rare earth elements of a weathering profile developed on tertiary greenstone belt in the extreme North Cameroon are reported. The aim of which was to investigate mineralogical evolution and element mobilization and redistribution during weathering under dry tropical climate. The weathering profile consists of four main horizons: (1) a spheroidal weathering zone constituted by a corestone–shell complex, (2) a C horizon, (3) a Bw horizon and an Ah horizon. The results indicate that nontronite, a Fe-rich smectite, is the exclusive clay mineral formed in the exfoliated shells and the C horizon. It is associated with kaolinite in the upper horizons. The coexistence of these two clay minerals induced a decrease of CEC and pH which becomes neutral. The weathering index (WI) values reveal that weathering becomes more and more intensive from the corestone up to Bw horizon, which is the most weathered horizon in the weathering profile. Mass balance calculations, using Th as immobile element, indicate that Ti is quite mobile and that Al and Fe are relatively enriched at the bottom and strongly leached at the top of the profile. Alkalis and alkaline earth elements are strong leached through out the profile, except Ca which displays similar trend as Al and Fe. The same goes for LILE (Cs, Sr), TTE (Cr, Co, Ni) and HSFE (Y, Nb, Hf). In opposite, REE are depleted at the bottom and enriched in the upper horizons, with more enrichment for LREE than for HREE. It appears that weathering of greenstone belt causes a fractionation of HREE and induces a concentration of LREEs. Ce and Eu anomalies display opposite behaviour.  相似文献   

Induced modifications of kaolinite under ionizing radiation: an infrared spectroscopic study     

C. Fourdrin  E. Balan  T. Allard  C. Boukari  G. Calas 《Physics and Chemistry of Minerals》2009,36(5):291-299

Radiation effects on kaolinite were investigated using He⁺ ions of 1.5 MeV at radiation doses up to 4.3 × 10⁸ Gy, which are comparable to the doses expected for clay barriers in high-level nuclear waste repositories. The concentration of paramagnetic radiation-induced defects in kaolinite reaches 2 × 10¹⁶ spins/mg (400 at. ppm), as determined by electron paramagnetic resonance spectroscopy. The broadening of X-ray diffraction patterns and transmission infrared (IR) absorption bands is mostly related to the structural strain induced by radiation-induced point defects. The broadening of IR absorption spectra is analyzed using an autocorrelation approach and is related to a change in the distribution of vibrational frequencies due to crystal heterogeneities. We theoretically analyze how the effective dielectric properties of kaolinite samples depend on macroscopic parameters and how irradiation can modify some of them. Irradiation leads to an increase in the electronic polarizability of kaolinite particles, related to the accumulation of radiation-induced electronic point defects.  相似文献   

Intercalation of kaolinite with acetamide     

R. L. Frost  J. Kristof  G. N. Paroz  J. T. Kloprogge 《Physics and Chemistry of Minerals》1999,26(3):257-263

Upon intercalation of both ordered (low defect) and disordered (high defect) kaolinites with acetamide, two types of interaction are observed. Firstly, hydrogen bonding between the NH₂ groups of the acetamide with the siloxane oxygens is formed, as evidenced by the formation of two new bands at 3400 and 3509 cm^–1. Secondly, the appearance of additional bands at ∼3600 cm^–1 in both the infrared and Raman spectra of the acetamide intercalates is attributed to a second type of hydrogen bonding by the interaction of the C=O group and the inner surface hydroxyls. Changes in the intensity of the hydroxyl deformation modes in the 895 to 940 cm^–1 region are attributed to the changes in the hydrogen bonding of the kaolinite surfaces. It is proposed that the hydrogen bonding between the adjacent kaolinite layers is replaced with hydrogen bonding between both kaolinite surfaces and the acetamide molecule. Changes in the molecular structure of acetamide are observed upon intercalation. The amide 1 band is lost and replaced with a well-defined NH₂ deformation vibration. The loss of the amide 1 band is attributed the hydrogen bond formation between the amide hydrogens and the siloxane surface. The bands of the C=O group at 1680 and 1740 cm^–1 become a single band at 1680 cm^–1. The amide 2 band remains unchanged. The lack of intensity of the 1740 cm^–1 band is attributed to the formation of hydrogen bonding between the inner surface hydroxyl groups and the carbonyl group. Received: 4 February 1998/ Revised, accepted: 30 June 1998  相似文献   

Diagenetic model of the Bajo Barreal formation (Cretaceous) in the southwestern flank of the Golfo de San Jorge Basin (Patagonia, Argentina)     

《Marine and Petroleum Geology》2017

This paper analyses the diagenetic evolution of sandstones belonging to the Bajo Barreal Formation (Cretaceous) in the Golfo de San Jorge Basin (Patagonia, Argentina). The Bajo Barreal Formation includes the main reservoirs, which are located along the western area of the basin and is composed of sandstones, conglomerates, mudstones, tuffaceous mudstones and some layers of tuffs. The principal reservoirs comprise medium-to coarse-grained sandstones, which are dominated by feldspathic litharenites and contain minor amounts of litharenites and lithic arkoses. The authigenic minerals include kaolinite, smectite, chlorite, quartz overgrowths, microquartz and calcite, with minor proportions of megaquartz, siderite, analcime, laumontite, feldspar overgrowths and illite/smectite and chlorite/smectite mixed layers. Secondary porosity is much more important than primary porosity and is produced by the dissolution of feldspar, lithic clasts and clay cements. The diagenetic history of the Bajo Barreal sandstones can be divided into seven diagenetic stages, each of which is characterized by a specific assemblage of authigenic minerals and diagenetic processes. Eogenetic conditions occur in stages 1, 2, 3 and 4. Stage 1 corresponds to shallow burial characterized by the physical reduction of primary porosity by compaction; during stage 2, rim clay cements of chlorite, smectite and clinoptilolite, as well as thin quartz overgrowths, were formed. The precipitation of pore-filling cements of kaolinite, chlorite and smectite occurred during stage 3, while stage 4 records the intense dissolution of feldspar, lithic fragments and kaolinite cements. Mesogenesis occurs in diagenetic stages 5 and 6. The former corresponds to a new phase of authigenic kaolinite, while the latter records the significant dissolution of feldspar, lithic clasts and previous cements, which produced the highest values of secondary porosity. Finally, stage 7 corresponds to the highest degree of diagenesis in the Bajo Barreal Formation (mesogenesis), which resulted in the precipitation of cements of zeolites and calcite, as well as quartz and plagioclase overgrowths.  相似文献