A neutron diffraction study of alkali cation migration in montmorillonites     

D. Gournis  A. Lappas  M. A. Karakassides  D. Többens  A. Moukarika 《Physics and Chemistry of Minerals》2008,35(1):49-58

Neutron powder diffraction measurements on lithium and cesium saturated montmorillonite samples before and after heat treatment at 300°C are studied, in order to undertake a complete refinement of crystal structure and unravel the migration mechanism for the interlayer cations of Li or Cs. Rietveld analysis of the corresponding diffraction patterns finds that montmorillonite crystallizes in the C2/m space group with unit cell dimensions consistent with the size of the specific interlayer cation. We show that thermal treatment affects the two types of samples in a different way. This is with respect to their unit cell dimensions and the migration of Li from the 2b to the 2c clay lattice site, in constrast to the Cs positioning which remains effectively unchanged.  相似文献   

Difference characteristics of sea surface temperature observed by GLI and AMSR aboard ADEOS-II     

Kohtaro Hosoda  Hiroshi Murakami  Akira Shibata  Futoki Sakaida  Hiroshi Kawamura 《Journal of Oceanography》2006,62(3):339-350

This study compares infrared and microwave measurements of sea surface temperature (SST) obtained by a single satellite. The simultaneous observation from the Global Imager (GLI: infrared) and the Advanced Microwave Scanning Radiometer (AMSR: microwave) aboard the Advanced Earth Observing Satellite-II (ADEOS-II) provided an opportunity for the intercomparison. The GLI-and AMSR-derived SSTs from April to October 2003 are analyzed with other ancillary data including surface wind speed and water vapor retrieved by AMSR and SeaWinds on ADEOS-II. We found no measurable bias (defined as GLI minus AMSR), while the standard deviation of difference is less than 1°C. In low water vapor conditions, the GLI SST has a positive bias less than 0.2°C, and in high water vapor conditions, it has a negative (positive) bias during the daytime (nighttime). The low spatial resolution of AMSR is another factor underlying the geographical distribution of the differences. The cloud detection problem in the GLI algorithm also affects the difference. The large differences in high-latitude region during the nighttime might be due to the GLI cloud-detection algorithm. AMSR SST has a negative bias during the daytime with low wind speed (less than 7 ms⁻¹), which might be related to the correction for surface wind effects in the AMSR SST algorithm.  相似文献   

The near infrared camera on the W.M. Keck telescope     

K. Matthews  B. T. Soifer 《Experimental Astronomy》1994,3(1-4):77-84

The near infrared camera (NIRC) was used for a science demonstration run on the Keck telescope during 16–24 March 1993. The camera used a 256×256 InSb array manufactured by Santa Barbara Research Corporation. Observations were obtained using narrowband and broad band filters from 1 to 2.4 microns, and grisms with a spectral resolution of 0.6 percent in the J, H and K atmospheric windows. The instrument was fully background limited over the entire wavelength range. The sky background was quite low, reaching 14.3 mag/square arc sec in the broadband K _s filter. The image quality of the camera + telescope was excellent, being seeing limited in the range 0.5–0.9.The science demonstration observations of the NIRC on the Keck Telescope included observations of the most distant galaxy known, 4C41.17 at a redshift z=3.8 and the most luminous object known, the IRAS source FSC10214+4724 at a redshift z=2.29. Observations of the radio galaxy address the problem of the alignment effect in high redshift radio galaxies as well as the environments of such systems. FSC10214+4724 appears to be a merging galaxy that is at least 5×10⁸ years old.Based on observations obtained at the W.M.Keck Observatory, which is operated jointly by the California Institute of Technology and the University of CaliforniaThe W.M. Keck Observatory is operated as a scientific partnership between the California Institute of Technology and the University of California. It was made possible by the generous gift of the W.M. Keck foundation and the support of its president, Howard Keck.  相似文献   

LonGSp: A near infra-red spectrometer     

S. Gennari  L. Vanzi 《Experimental Astronomy》1994,3(1-4):191-192

We present a new cooled grating near infra-red spectrometer designed to acquire spectra at the TIRGO telescope in the 0.9÷2.5m region with a resolving power of 300÷4000, equipped with a Rockwell NICMOS 3 detector.  相似文献   

Fluid salinities obtained by infrared microthermometry of opaque minerals: Implications for ore deposit modeling — A note of caution     

Robert Moritz   《Journal of Geochemical Exploration》2006,89(1-3):284

Infrared microthermometry of opaque minerals has revealed that temperatures of phase changes vary with the infrared light source intensity, resulting in an overestimate of fluid salinities and an underestimate of homogenization temperatures. Failing to recognize this analytical artifact during infrared microthermometry may result in meaningless geological models. A fluid inclusion investigation on enargite from a high-sulfidation epithermal deposit is used as an example to document this. Fluid salinities obtained during an early investigation ranged between 6.3 and 20.4 wt.% NaCl, which were interpreted as intense boiling or as evidence for the involvement of a magmatic brine during ore formation. Fluid inclusion salinities obtained with improved analytical settings, i.e. low light intensities, fall between 1.1 and 1.7 wt.% NaCl and are in better agreement with fluid salinities obtained in quartz from similar deposits, and recent modeling suggesting vapor transport of Au and Cu from deep porphyry-Cu environments to shallower high-sulfidation epithermal deposits.  相似文献   

Neutron irradiation and post-irradiation annealing of rutile (TiO2−x ): effect on hydrogen incorporation and optical absorption     

Geoffrey David Bromiley  Andrei A. Shiryaev 《Physics and Chemistry of Minerals》2006,33(6):426-434

Neutron irradiation and post-irradiation annealing under oxidising and reducing conditions have been used to investigate H incorporation in, and the optical properties of, reduced (TiO_2−x ) rutile. Optical absorption in rutile is mainly due to a Ti³⁺ Ti⁴⁺ intervalence charge transfer effect. The main mechanism for H incorporation in rutile involves interstitial H not coupled to other defects, which has important implications for the rate of H diffusion, and possibly also on the electrical properties of rutile. Additional minor OH absorption bands in IR spectra indicate that a small amount of interstitial H is coupled to defects such as Ti³⁺ on the main octahedral site, and indicates that more than one H incorporation mechanism may operate. Concentration of oxygen vacancies has a controlling influence on the H affinity of rutile.  相似文献   

Synchrotron IR study of hydrous ringwoodite (γ-Mg2SiO4) up to 30 GPa     

E. M. Chamorro Pérez  I. Daniel  J.-C. Chervin  P. Dumas  J. D. Bass  T. Inoue 《Physics and Chemistry of Minerals》2006,33(7):502-510

High-pressure synchrotron infrared (IR) absorption spectra were collected between 650 and 4,000 cm⁻¹ at ambient temperature for hydrous Mg-ringwoodite (γ-Mg₂SiO₄) up to 30 GPa. The main feature in the OH⁻ stretching region is an extremely broad band centred at 3,150 cm⁻¹. The hydrogen bond is strong for most protons and the most probable site for protonation is the tetrahedral edge. With increasing pressure, this band shifts downward while decreasing its integrated intensity until disappearance at a pressure of 25 GPa. Only one band at 2,450 cm⁻¹ and an absorption plateau persist with a maximum wavenumber of 3,800 cm⁻¹. This behaviour is reversible upon pressure release. We interpret this as a second-order phase transition occurring in hydrated Mg-ringwoodite at high pressure (beyond ∼ 25 GPa). This result is compatible with the observation by Kleppe et al. (Phys Chem Miner 29:473–476, 2002a) who suggested the presence of Si–O–Si linkages and/or partial increase in the coordination of Si. Beyond the phase transition, the protons are delocalized and their environment on the ringwoodite structure is probably quite different from that at low pressure. Data obtained in situ at high pressures and temperatures are needed to better understand the effect of protonation on the structure and to better constrain this phase transition.  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   

Petrology and geochemistry of a diamondiferous lherzolite from the Premier diamond mine, South Africa     

K.S. Viljoen  Ren Dobbe  Braam Smit  Emilie Thomassot  Pierre Cartigny 《Lithos》2004,77(1-4):539-552

This paper reports on the petrology and geochemistry of a diamondiferous peridotite xenolith from the Premier diamond mine in South Africa.

The xenolith is altered with pervasive serpentinisation of olivine and orthopyroxene. Garnets are in an advanced state of kelyphitisation but partly fresh. Electron microprobe analyses of the garnets are consistent with a lherzolitic paragenesis (8.5 wt.% Cr₂O₃ and 6.6 wt.% CaO). The garnets show limited variation in trace element composition, with generally low concentrations of most trace elements, e.g. Y (<11 ppm), Zr (<18 ppm) and Sr (<0.5 ppm). Garnet rare earth element concentrations, when normalised against the C1 chondrite of McDonough and Sun (Chem. Geol. 120 (1995) 223), are characterised by a rare earth element pattern similar to garnet from fertile lherzolite.

All diamonds recovered are colourless. Most crystals are sharp-edged octahedra, some with minor development of the dodecahedral form. A number of crystals are twinned octahedral macles, while aggregates of two or more octahedra are also common. Mineral inclusions are rare. Where present they are predominantly small black rosettes believed to consist of sulfide. In one instance a polymineralic (presumably lherzolitic) assemblage of reddish garnet, green clinopyroxene and a colourless mineral is recognised.

Infrared analysis of the xenolith diamonds show nitrogen contents generally lower than 500 ppm and variable nitrogen aggregation state, from 20% to 80% of the ‘B’ form. When plotted on a nitrogen aggregation diagram a well defined trend of increasing nitrogen aggregation state with increasing nitrogen content is observed. Carbon isotopic compositions range from −3.6 ‰ to −1.3 ‰. These are broadly correlated with diamond nitrogen content as determined by infrared spectroscopy, with the most negative C-isotopic compositions correlating with the lowest nitrogen contents.

Xenolith mantle equilibration temperatures, calculated from nitrogen aggregation systematics as well as the Ni in garnet thermometer are on the order of 1100 to 1200 °C.

It is concluded that the xenolith is a fertile lherzolite, and that the lherzolitic character may have resulted from the total metasomatic overprinting of pre-existing harzburgite. Metasomatism occurred prior to, or accompanied, diamond growth.  相似文献   

Polymorphic phase transition in Superhydrous Phase B     

M. Koch-Müller  P. Dera  Y. Fei  H. Hellwig  Z. Liu  J. Van Orman  R. Wirth 《Physics and Chemistry of Minerals》2005,32(5-6):349-361

We synthesized superhydrous phase B (shy-B) at 22 GPa and two different temperatures: 1200°C (LT) and 1400°C (HT) using a multi-anvil apparatus. The samples were investigated by transmission electron microscopy (TEM), single crystal X-ray diffraction, Raman and IR spectroscopy. The IR spectra were collected on polycrystalline thin-films and single crystals using synchrotron radiation, as well as a conventional IR source at ambient conditions and in situ at various pressures (up to 15 GPa) and temperatures (down to −180°C). Our studies show that shy-B exists in two polymorphic forms. As expected from crystal chemistry, the LT polymorph crystallizes in a lower symmetry space group (Pnn2), whereas the HT polymorph assumes a higher symmetry space group (Pnnm). TEM shows that both modifications consist of nearly perfect crystals with almost no lattice defects or inclusions of additional phases. IR spectra taken on polycrystalline thin films exhibit just one symmetric OH band and 29 lattice modes for the HT polymorph in contrast to two intense but asymmetric OH stretching bands and at least 48 lattice modes for the LT sample. The IR spectra differ not only in the number of bands, but also in the response of the bands to changes in pressure. The pressure derivatives for the IR bands are higher for the HT polymorph indicating that the high symmetry form is more compressible than the low symmetry form. Polarized, low-temperature single-crystal IR spectra indicate that in the LT-polymorph extensive ordering occurs not only at the Mg sites but also at the hydrogen sites.  相似文献