The development of radio astronomy at Hartebeesthoek

The development of radio astronomy at the Hartebeesthoek Radio Astronomy Observatory in South Africa is described. The Hartebeesthoek site was established originally by NASA as one of three Deep Space Stations equipped with 26-m parabolic reflector antennas. It was first used for radio astronomy by South Africa in terms of the NASA host nation agreement which allowed for its use at times when the facility was not needed for its primary purpose of tracking space probes. After NASA withdrew from South Africa in 1975, the South African Council for Scientific and Industrial Research took over the site and the 26-m parabolic reflector antenna, which NASA had abandoned in position, and established it as a national observatory. The development of the facility to the stage where it could support a variety of observing programmes such as continuum observations and mapping, spectroscopy and pulsar timing is described as well as the role played by the Observatory in global programmes of very long baseline interferometry.     

X-ray spectroscopy of stellar coronae

Summary From the early discovery in 1948 of X-rays from the Solar corona, X-ray spectroscopy has proven to be an invaluable tool in studying hot astrophysical and laboratory plasmas. Because the emission line spectra and continua from optically thin plasmas are fairly well known, high-resolution X-ray spectroscopy has its most obvious application in the measurement of optically thin sources such as the coronae of stars. In particular X-ray observations with theEINSTEIN observatory have demonstrated that soft X-ray emitting coronae are a common feature among stars on the cool side of the Hertzsprung-Russell diagram, with the probable exception of single very cool giant and supergiant stars and A-type dwarfs. Observations with the spectrometers aboardEINSTEIN andEXOSAT have shown that data of even modest spectral resolution (/ = 10–100) permit the identification of coronal material at different temperatures whose existence may relate to a range of possible magnetic loop structures in the hot outer atmospheres of these stars. The higher spectral resolution of the next generation of spectrometers aboard NASA'sAXAF and ESA'sXMM will allow to fully resolve the coronal temperature structure and to enable velocity diagnostics and the determination of coronal densities, from which the loop geometry (i.e. surface filling factors and loop lengths) can be derived. In this paper various diagnostic techniques are reviewed and the spectral results fromEINSTEIN andEXOSAT are discussed. A number of spectral simulations forAXAF andXMM, especially high-resolution iron K-shell, L-shell, and2s-2p spectra in the wavelength regions around 1.9 Å, 10 Å, and 100 Å, respectively, are shown to demonstrate the capabilities for temperature, density, and velocity diagnostics. Finally, iron K-shell spectra are simulated for various types of detectors such as microcalorimeter, Nb-junction, and CCD.     

Micro-spectroscopic investigations of highly heterogeneous waste repository materials

Assuring safe disposal and long-term storage of radioactive and toxic wastes corresponds to a primary environmental task of present societies. To improve any technical limitation, a mechanistic understanding of the processes governing the binding of heavy metals and radionuclides is required. In this study, the significance of synchrotron-based X-ray microprobes for elucidating the spatial distribution and the speciation of radionuclides in highly heterogeneous waste repository materials will be outlined. A case study on the uptake process of Co in cementitious engineered barrier materials exposed to microbial degradation will be presented.     

Characterization of cristobalite in ash and dome rock from the Soufriere Hills volcano, Montserrat： Implications for respiratory health hazards

A link between the inhalation of respirable silicas （SiO2） and respiratory diseases such as silicosis is widely recognized. Ash from dome collapse eruptions on Montserrat has been found to contain high levels （〉20%） of silicas in the form of cristobalite, tridymite, quartz and/or amorphous silica. The toxicity of these silica polymorphs varies widely. Cristobalite and quartz （tridymite less well established） are viewed as carcinogenic to humans whereas amorphous silica generally shows a reduced biological response. In assessing the potential health effects of volcanic ash particulates it is vital to determine the types and concentration of silicas as well as their size （respirable fraction）, shape and surface properties. The aim of this study is to develop methods to assess potentially toxic respirable airborne silicas in the dome collapse ash （applicable to a range of ash types） and to develop a model to predict the levels and types of respirable silicas from future eruptions. The model is being developed by comparing dome rock with related ash from a series of previous eruption events. Mineralogical assessment using conventional scanning X-ray diffraction （XRD） was hampered by difficulties in differentiating characteristic peaks for cristobalite and tridymite in complex multi-component ash samples （containing high levels of plagioclase）. These difficulties have been largely overcome using an Enraf-Nonius PDS120 diffractometer with curved （120 degrees 20） position sensitive detector （PSD）. The determination of size, shape and elemental characteristics of ash particulate and dome rock samples has been carried out using automated analytical scanning electron microscopy. The quantification of mineral proportions using PSD-XRD was highly successful with an accuracy of 1 to 2 wt%. However, the determination of phase proportions using automated analytical SEM was problematic due to scattering effects and the multiphase nature of many of the particles.     

In situ time resolved synchrotron powder diffraction study of thaumasite

Structural changes during dehydration and subsequent decomposition in thaumasite Ca₃Si(SO₄)(CO₃)(OH)₆·12 H₂O were studied by in situ synchrotron powder diffraction between 303 and 1,098 K. Evolution of the crystal structure was observed through 28 structure refinements, by full profile Rietveld analysis performed in the P6₃ space group, between 300 and 417 K, whereupon the thaumasite structure was observed to breakdown. Within this temperature range, the cell parameters of thaumasite increased as a function of temperature in a nearly linear fashion up to about 393 K, at which temperature, a slight slope change was observed. Above 400 K, the thermogravimetric analysis revealed that the dehydration process proceeded very rapidly while the refined occupancy of water molecules dropped below a critical level, leading to instability in the thaumasite structure. At a same time, a remarkable change in the unit cell parameters occurring at about 417 K indicated that the crystal structure of thaumasite collapsed on losing the crystallization water and it turned amorphous. This result indicated that the dehydration/decomposition of thaumasite was induced by the departure of the crystallization water. At about 950 K, anhydrite and cristobalite crystallized from the thaumasite glass.     

Alteration, evaluation and use of extremaduran granite residues

The necessity of eliminating debris from a granite quarry has awakened an interest in applications of by-products, called “marginal arids”, in different fields, like construction and foundations for roadways, restoration, material for the manufacture of artificial rocks, and artesian products etc. Conclusions obtained from the results of tests carried out by X-ray diffraction of granite quarry by-products in Extremadura, Spain, submitted to different treatments, are established. Test pieces from two quarries are analyzed and compared generally and specifically, for commercial use. Finally, conclusions relating to essays in test pieces and mineral dynamics of marginal arid granite are exposed.     

The effect of composition and cation ordering on the compressibility of columbites up to 7 GPa

The unit-cell parameters of two columbite samples along the (Fe,Mn)Nb₂O₆ solid solution were measured by means of high-pressure single-crystal X-ray diffraction up to pressures of 7 GPa. The compressional behaviour of these minerals was studied as a function of composition and degree of order. The P–V data of all the samples were fitted with a third-order Birch–Murnaghan equation of state. For the two samples with different compositions but identical degree of order the substitution of Mn for Fe causes a decrease of the bulk modulus K _T0, from 153(1) to 146(1) GPa, without any effect on the pressure first derivative K′. For the two samples with the same composition, cation ordering causes an increase of the bulk modulus from 149(1) to 153(1) GPa and of the pressure first derivative from 4.1(2) to 4.8(3). The compressional behaviour is anisotropic with a linear axial compressibility scheme β _b > β _c ≥ β _a for all samples, regardless of composition and degree of order. Such anisotropy increases sligthly with increasing Mn content.     

The effect of thermal treatment on the 57Fe Mössbauer spectrum of beryl

Mössbauer spectra (MS) of blue, green and yellow beryl (ideally Be₃Al₂Si₆O₁₈) containing approximately 1% of iron were obtained at 295 and 500 K. Room temperature (RT) spectra of both blue and green samples showed the presence of an asymmetric Fe²⁺ doublet (ΔE _Q~2.7 mm/s, δ~1.1 mm/s), with a very broad low-velocity peak. There is no clear evidence for the presence of a ferric component. The MS of the yellow sample at RT consists of an intense central absorption with parameters typical for Fe³⁺ (ΔE _Q~0.4 mm/s, δ~0.29 mm/s), plus an apparently symmetrical Fe²⁺ doublet. This sample acquires a light-blue shade upon heating in air at about 620 K. Thermal treatments at high temperatures caused no significant changes in the MS, but the green and yellow beryl acquire a blue colour. All these results are interpreted in relation to the existence of channel water and the distribution of iron among the available crystallographic sites.     

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

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.     

微量相X射线衍射定量分析的一种简便方法

阐述了关于微量相X射线衍射定量分析的一种简便方法———近似线性关系法,它适用于二相体系(或基体吸收系数基本恒定的多相体系)材料中微量相的定量分析。该方法不需要在待测样品中加入参考物相,分析时仅需对一条衍射线进行测定,因而分析时间很短,其测定结果与实际含量的相对误差为-10.2%～ 21.4%,与外标法和内标法的测量结果的精度相当。