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1.
Recent experimental studies have shown that the rates of Al–Si order-disorder and interdiffusion in alkali feldspars at high pressures under dry conditions increase dramatically in the approximate pressure range 7–14 kb, depending on temperature and feldspar composition (Goldsmith 1987, 1988). Enhancement of Al–Si interdiffusion rates is ascribed to the involvement of hydrogen, but the species of hydrogen involved is undetermined.A simple kinetic analysis of the data of Goldsmith (1987) on disordering of dry albite at 800°–950° C and 6–24 kb in the solid media press is consistent with the NaCl pressure cell acting as a proton donor by enhancing dissociation of water in the pressure medium, generating a high in the experimental environment. The rate constant for disordering of albite is found to increase linearly with the estimated experimental and with the density of aqueous salt solution, implicating H+ as the rate-enhancing species.Further experimental studies confirm the importance of . At 16 kb and 850° C, dry albite in sealed Pt capsules in a NaCl cell containing tantalum powder (which reduces H2O to H2) remains highly ordered over the same time that complete disordering would occur in the absence of Ta. H2 cannot therefore be the rate-enhancing species. At 1 kb and 850° C, the extent of Al–Si disorder in albite in direct contact with various NaCl–H2O solutions increases from partially disordered for pure H2O to completely disordered for saturated aqueous NaCl solution, giving strong support to the proton model. SIMS scanning ion imaging of albite run products demonstrates conclusively that solution-reprecipitation is not responsible for enhanced disordering rates.Results of disordering experiments in the solid media apparatus cannot be duplicated in Ar gas media internally-heated pressure vessels, even with the same experimental configuration around the albite-bearing capsules, due to the different proton-buffering capacities of the solid and gas media apparatus.  相似文献   

2.
 X-band electron paramagnetic resonance experiments on a gamma-irradiated α-quartz crystal have revealed a new hydrogarnet-like defect. Analysis of the spectral data suggests that the centre consists of an oxygenic electron hole adjacent to a silicon vacancy, charge-compensated by a proton and two lithium +1 ions. The principal directions of the spin-Hamiltonian g matrix indicate that the oxygenic hole occurs on the oxygen ion that would be long-bonded to the missing silicon atom. Modelling of the proton and lithium hyperfine matrices via three different methods has provided a detailed physical view for the structure of the defect centre, which is presented here. Received: 12 June 2002 / Accepted: 10 January 2003 RID="‡" ID="‡" Deceased August 2001  相似文献   

3.
From primitive wood to nowadays fossil fuels such as coal, oil and natural gas, it can be seen that the forms of energy becomes more and more diverse and the core trend of decarburization is also obvious （the rate of the element of H to C ranging from 1/10, 1/2-1, 2, to 4 in wood, coal, oil and natural gas, respectively）. Although the content of C in current main fuels becomes less and less, the excess exploitation and extensive utilization of various fossil fuels are widely recognized to be responsible for the deterioration of the environment （greenhouse effect, acid rain, photochemical pollution, etc.）. With the roar consumption of energy to maintain the development of human society and taking the environmental problems into consideration, it is inevitable to develop renewable energy containing more H and less C as possible. Under these circumstances, the development of H2 energy is the certain and ultimate choice for its high energy per unit, diversity resources, no pollution to environment and ideal renewable utilization cycle. There are so many methods and ways were employed to develop HE energy, such as electrolysis, methane stream reforming process, coal gasification, etc., but there lies two main problems in current methods and ways, those are the cost of bulk of first energy to extract HE from fossil raw materials and still facing the problems of C deposition （carbon dioxide）. Consequently, if considering the cost and environmental issues, the development of HE energy must resort to renewable energy sources such as solar energy, wind energy to extract HE from water. Based on this context, the development of HE energy by semiconductor photocatalyst to split water into HE and O2 under the irradiation of solar energy, photocatalysis process in short word, is one of the most promising ways. In this review, the importance and necessity to develop hydrogen energy were intensively studied based on the relationship between energy consumption and environment effect. Then the current ways and methods to develop hydrogen were reviewed, especially the state-of-the-art photocatalysis process （from the semiconductor photocatalyst materials perspective）.  相似文献   

4.
The thermally induced reductive decomposition of a natural near end-member almandine [VIII(Fe2.85Mg0.11Ca0.05Mn0.02)VI(Al1.99)IV(Si2.99)O12] and possible hydrogen diffusion into its structure have been carried out at temperatures up to 1,200°C, monitored by simultaneous thermogravimetric analysis and differential scanning calorimetry (DSC), infrared and 57Fe Mössbauer spectroscopy and X-ray powder diffraction. Below 1,000°C, evidence for hydrogen diffusion into almandine structure was not observed. At temperatures above 1,000°C, reductive decomposition sets in, as displayed by a sharp endothermic peak at 1,055°C on the DSC curve accompanied by a total mass loss of 3.51%. We observe the following decomposition mechanism: almandine + hydrogen → α-Fe + cristobalite + hercynite + water. At higher temperatures, fayalite and sekaninaite are formed by consecutive reaction of α-Fe with cristobalite and water, and cristobalite with hercynite, respectively. The metallic α-Fe phase forms spherical and isolated particles (~1 μm).  相似文献   

5.
Increased interest in paleoenvironmental studies is a result of climatic changes occurring at present and predicted for the future. Such studies could be done using the stable isotope compositions (δ2H and δ18O) of kaolins, which provide knowledge on the paleoenvironmental conditions prevailing during the time of kaolinisation. In this study, the stable isotopic compositions of clay-size fraction of kaolins occurring in Cretaceous and Tertiary Formations of the Douala Sub-Basin in Cameroon are presented, with the aim of reconstructing the paleoenvironmental conditions of the Sub-Basin. To achieve this, the clay-size fraction (< 2 μm fraction) of 8 kaolinite-rich samples were analysed for their δ2H and δ18O compositions, and results were reported as part per mil (‰) relative to the SMOW standard. The δ18O values of kaolins found in the Cretaceous–Tertiary Formations of the Douala Sub-Basin varied between +18.2 and +21.0‰, whereas the δ2H values varied between –69 and –53‰. Nine of the eleven samples plotted on the right of the supergene–hypogene line. Five of these nine samples plotted very close to the kaolinite line, which represents the composition of kaolinite in equilibrium with meteoric water at 20 °C; suggesting a supergene weathering origin of these kaolins. The determination of the temperature of kaolinisation yielded mean formation temperatures of 22 ± 2 °C and 27 ± 6 °C for Cretaceous and Tertiary kaolins, respectively. Excluding the two samples falling in the hypogene field, averages of kaolinisation temperatures were 20 and 25 °C during the Cretaceous and Tertiary periods, respectively. These temperatures are slightly below the present mean annual temperature in Douala (27 °C), thereby suggesting that the climate was becoming warmer from the Cretaceous to the Present. Therefore, Douala had a cooler and rainy climate during the Cretaceous, and the climate is gradually becoming hotter and more humid, favouring the refinement of existing kaolins and the kaolinisation of kaolin-forming minerals in the Sub-Basin.  相似文献   

6.
The nicotinamide (pyridine-3-carboxamide, nia) complexes of silver(I), [Ag(nia)2(NO3)]·H2O (1), [Ag(nia)2(NO3)] (2), and {K[Ag(nia)2](NO3)2} n (3), were prepared and characterised by IR spectroscopy and TG/DTA thermal methods. The solid state structures of 2 and 3 were determined by single-crystal X-ray diffraction analysis. In both complexes two nicotinamide ligands are coordinated to silver(I) through the nitrogen atom of the pyridine ring in a near-linear fashion. In 2, additional coordination by two oxygen atoms of one nitrate group leads to the distorted tetrahedral coordination environment of silver(I). In 3, nitrate ions bridge potassium cations giving rise to a 2D coordination network which is further stabilised by cross-bridging of each two potassium atoms in [1 0 0] direction by complex cations, [Ag(nia)2]+. Despite different aggregation of 2 and 3 in the solid state, both complexes demonstrate quite similar thermal stability. The amide self-complementary hydrogen bonds appear to be the main driving force for establishing the crystal structures of both 2 and 3.  相似文献   

7.
Interdiffusion of Fe and Mg in (Mg,Fe)O has been investigated experimentally under hydrous conditions. Single crystals of MgO in contact with (Mg0.73Fe0.27)O were annealed hydrothermally at 300 MPa between 1,000 and 1,250°C and using a Ni–NiO buffer. After electron microprobe analyses, the dependence of the interdiffusivity on Fe concentration was determined using a Boltzmann–Matano analysis. For a water fugacity of ∼300 MPa, the Fe–Mg interdiffusion coefficient in Fe x Mg1−x O with 0.01 ≤ x ≤ 0.25 can be described by with and C = −80 ± 10 kJ mol−1. For x = 0.1 and at 1,000°C, Fe–Mg interdiffusion is a factor of ∼4 faster under hydrous than under anhydrous conditions. This enhanced rate of interdiffusion is attributed to an increased concentration of metal vacancies resulting from the incorporation of hydrogen. Such water-induced enhancement of kinetics may have important implications for the rheological properties of the lower mantle.
Sylvie DemouchyEmail:
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8.
The structures of deuterated pyrochroite, Mn(OD)2 and β−Cο(OD)2 have been refined using the Rietveld method and neutron powder diffraction data collected in an opposed-anvil high pressure (Paris-Edinburgh) cell from room pressure to 9 GPa. The equation of state for Mn(OD)2 was determined (K=41(3) GPa for fixed K′=4.7) and found to be consistent with previous studies of the isostructural brucite, Mg(OD)2. The compressibility of β−Cο(OD)2 on the other hand is apparently anomalous. The c-axis initially decreases at 3 times the rate of decrease of the a-axis; the ratio decreases to about 1.5 at an estimated 6 GPa before increasing again beyond this pressure. There is no obvious corresponding anomaly in the details of the atomic structure. In both materials there is an increase in the D-site disorder with pressure. A split-site model for the D-positions best fits the data at pressures above 8 GPa. There is no statistically significant increase in the O-D interatomic distance at increased pressure while the hydrogen bonding interaction D...O appears to increase as this distance decreases and the O-D...O angle increases. The intramolecular O-D bond valences, determined indirectly from the intermolecular D...O distances, decrease steadily for both materials as pressure is increased. Received: 31 October 1996 / Revised, accepted: 27 February 1997  相似文献   

9.
The direct determination of most trace elements in natural water samples is still very difficult even if the high-sensitivity atomic analytical instrument, such as ICP-MS, is available. The reasons are (1) the natural concentrations of most trace elements…  相似文献   

10.
1 IntroductionIncorporation of potentially toxic metals ( e.g.Cd, Cu, Cr, Pb, Hg, As, Se, Zn, Ni) into soils ei-ther through sewage-sludge irrigation or some othersources of pollution (e.g. atmospheric deposition, ap-plication of agri-chemicals) has posed…  相似文献   

11.
The volumes per oxygen of some silicate melts have been calculated and then compared with those of silicate glasses.It is suggested that the volume of a silicate melt can be divided into two parts.One is contri buted by the silicon-oxygen network and the other by the “oxides”.Variation patterns of VPOs suggest that the volume of the Si-O network generally remains unchanged and the expansion of the melt is caused mainly by the locat expansion of the “oxides”.It is further proposed that the radius of O^2- shows little variation,in striking contrast to the radius of cations.The mechanism governing the expansion is discussed in detail.  相似文献   

12.
Granitoids are widely spread in the Nanling Region of China.Four rockbodies in the region the been studied for their REE,Rb,Sr,Ba and Sc distributions.The four rockbodies occurred in different locations and are characterized as being different in age and type.The rock types are presented as follows:Qinghu monzonite,Guangxi;Fuxi granodiorite,Guangdong;Jiufeng monzonitic granite,Hunan;Zudong K-feldspar granite,Jiangxi.From the major and trace element distributions in these granitoids it is clearly shown that Rb/Sr ratios in the rocks tend to increase with increasing SiO2 content and differentiation index(DI),but LREE/HREE,La/Yb and K/Rb ratios tend to decrease,suggesting a correlation between trace element distribution and major element composition for the granitoids.The distribution characteristics of trace elements in each of the rockbodies are described in detail.From the comparative analysis of the Qinghu monzonite and Fuxi granodiorite it is evidenced that the REE distribution is closely related to the sequence of crystallization for the minerals,and also to the petrochemical types of these granitoids in addition to their crystal chemistry.  相似文献   

13.
The author studied the grain size, shape, colour, altered coat, mineral species, chemical composition,end- member components and infrared spectra of clinopyroxenes occurring as megacryst, macrocryst andgroundmass minerals, intergrowths with pyrope and ilmenite and minerals in deep-seated xenoliths and inclu-sions in diamonds in kimberlites of China. The clinopyroxenes under study were compared with megacrystclinopyroxenes in basalts and minerals in their deep-seated xenoliths and clinopyroxenes in lamproites andminettes. The coexisting clinopyroxene-pyrope pair was studied. Besides the author also studied the origin ofclinopyroxenes in kimberlites, P-T conditions for their formation and their reflected tectonic environments ofthe kimberlite formation. He suggests that this mineral is an indicator for diamond exploration.  相似文献   

14.
The study of the physicochemical behaviour of colloids and particles in nature has emerged as a scientific problem of critical importance because of the widespread acknowledgement of their significance in controlling the speciation and fate of essential nutrients and contaminants in the aquatic and soil environments （Ledin et al., 1995; Lead et al., 1999, Doucet et al., 200 l; McCarthy et al., 1989; Koterba et al., 1993; Kretzschmar et al., 1999）. Se＇quaris and Lewandowski （2003） developed a method based on sedimentation and centrifugation steps to fractionate agricultural top soils after suspension in water. However, progress in the field has been limited by the lack of appropriate techniques for the isolation and characterization of colloids and particles in their native form （Lead et al., 1997）. The primary difficulties in separation and analysis are colloidal instability and their small size and low concentration. As a result, reliable, unbiased and minimally perturbing methods for sampling and fractionation are primary requirements for the study of colloids and particles if valuable information is to be obtained. In recent years, cross-flow ultra-filtration （CFUF） has become one of the most commonly used techniques for collecting and separating freshwater and marine colloids and particles （Petrus evski et al., 1995; Gustafsson et al., 1999; Benoit et al., 1999; Sigg et al., 2000; Gue＇guen et al., 2002; Benedetti et al., 2003）. CFUF has hitherto been used for studies of the biogeochemical cycling of a variety of elements, such as carbon （Benner et al., 1992; Santschi et al., 1998）, radionuclides （Moran et al., 1992）, trace metals （Reitmeyer et al., 1996） and nutrients （Bauer et al., 1996）. The purpose of this study was to develop a protocol to fractionate particles in soil, to measure particle size distributions and to quantify chemical characteristics within different particle size fractions.  相似文献   

15.
By experimental data on the concentration of toxic microelements (Pb, Cd, Cu, Zn, Ni, Co, and Cr) in atmospheric aerosols over the White and Norwegian Seas in winter-spring period of 2009–2010, the contamination of air environment over two sea basins, significantly different by geographical conditions but being heavily impacted by North-European industrial centres, including the impact of the largest in the European Arctic Kola industrial centre, has been analyzed. It has been indicated and described that the air basin over the White Sea water area, when compared to the Norwegian Sea, is under a significantly greater impact of the emission sources of heavy metals, located on the Kola Peninsula.  相似文献   

16.
Although inorganic species are predominant in natural systems, but there are many kinds of organoarsenic species such as methylated and phenylated arsenic compounds. Phenylarsonic acid （PA） is a degradation product of organoarsenics used for chemical warfare agents, which has been detected in well water at the disposal site of the agents in Japan. There are few reports studying behavior of PA in soil. In this study, PA was adsorbed onto ferrihydrite and its chemical forms were determined using high performance liquid chromatography connected to inductivity-coupled plasma mass spectrometry （HPLC-ICP-MS）. 100 mg/kg of PA was mixed with 0.03 g of 2-line ferrihydrite. For each suspension, pH was adjusted by HNO3 or NaOH. Each sample was incubated for more than 19 hours and the final pH was measured. After filtration, the chemical form of arsenic in the filtrate was measured using HPLC-ICP-MS. In addition, ferrihydrite separated by filtration was dissolved by 3 ml of 0.5 M HCI and the arsenic species in the solution was detected by HPLC-ICP-MS （column： Tosoh TSKgel SuperlC-AP, eluent： 0.01 M HNO3）. It was verified that PA is not degraded by heating in 0.5 M HCl solution. At pH 3.1, any arsenic compounds were not detected from the solution, because almost all arsenic species were adsorbed onto ferrihydrite at lower pH. At pH= 12, however, 7%-10% of inorganic arsenic was detected in the solution. In solid phase, there are some problems to determine the precise ratio of inorganic and organic species. When the solution includes Fe ion at 0.01 M level, the retention time of arsenic species drifted compared to those in standard solution, which makes it difficult to determine precisely the arsenic species adsorbed on ferrihydrite. Therefore, more study is needed to determine the ratio of inorganic and organic species in the system.  相似文献   

17.
Please refer to the attachment(s) for more details.  相似文献   

18.
The timing of the emplacement of ore-bearing melts in the process of evolution of flood-basalt magmatism in the Noril’sk District is discussed. The current models of ore formation consider the emplacement of ore-bearing intrusions either under the conditions of a closed magmatic system as a product of a self-dependent magmatic event, or under the conditions of an open magmatic system, where intrusions are parts of the conduits feeding lava flows. In both cases, the composition of the initial magma, the content of volatile components therein, and the contribution of country rock assimilation are important for the development of a genetic model. The relationships between lavas and intrusions are exemplified in the South Maslov intrusion, which cuts through the rocks of the Nadezhdinsky Formation. No geological evidence for links of lavas to intrusions has been established. Substantial difference in geochemistry (Ti contents, Gd/Yb and La/Sm ratios, etc.) of the tuff and lava sequence on the northern shore of Lake Lama and the Maslov intrusions are demonstrated. It is concluded that the Noril’sk deposits were formed as products of emplacement of self-dependent portion of magma in the post-lower Nadezhdinsky time. The melt composition determined from melt inclusions in olivine corresponds to high-Mg tholeiitic basalt (up to 7–8 wt % MgO) containing up to 1 wt % H2O and 0.3 wt % Cl and undersaturated with sulfur. The fluid regime of flood-basalt volcanism had no anomalous features—the fluid was aqueous-carbon dioxide. The melts of ore-bearing and barren intrusions had similar concentrations of volatile components. The distribution of major and trace elements in intrusive rocks of the contact zone with the lower part of the Nadezhdinsky Formation characterized by high (La/Sm)N ratio in comparison with gabbroic rocks (2.8–2.3 and 1.3–1.6, respectively), indicates that contamination of the initial melt only took place in a narrow (1 m) contact zone or did not develop at all. New data on isotopic compositions of Sr (87Sr/86Sr)251 = 0.7089 and Pb (206Pb/204Pb = 20.877–24.528 in anhydrite confirm that local assimilation did not play a substantial role in the formation of rock and ores. On the basis of chemical composition of ore-forming intrusions, their isotopic characteristics, and the composition of melt inclusions in olivine, it is suggested that the lower crustal rocks were a major source of ore-bearing magmas.  相似文献   

19.
Please?refer?to?the?attachment(s)?for?more?details.  相似文献   

20.
Acta Geologica Sinica (hereinafter referred to as the Acta) starting publication in 1922, is a quaterly academia periodical sponsored by the Geological Society of China (GSC). It has been one of the science and technology periodicals in China with the longest history.  相似文献   

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