The kinetics of the dehydroxylation of chrysotile was followed in situ at high temperature using real-time conventional and
synchrotron powder diffraction (XRPD). This is the first time kinetics parameters have been calculated for the dehydroxylation
of chrysotile. The value of the order of the reaction mechanism calculated using the Avrami model indicates that the rate-limiting
step of the reaction is a one-dimensional diffusion with an instantaneous nucleation or a deceleratory rate of nucleation
of the reaction product. Hence, the rate-limiting step is the one-dimensional diffusion of the water molecules formed in the
interlayer region by direct condensation of two hydrogen atoms and an oxygen atom. The calculated apparent activation energy
of the reaction in the temperature range 620–750 °C is 184 kJ mol−1. The diffusion path is along the axis of the fibrils forming the fibers. The amorphous or short-range ordered dehydroxylate
of chrysotile is extremely unstable because forsterite readily nucleates in the Mg-rich regions. Moreover, it is less stable
than the dehydroxylate of kaolinite, the so-called metakaolinite, which forms mullite at about 950 °C. This difference is
interpreted in terms of the different nature of the two ions Mg2+ and Al3+ and their function as glass modifier and glass-forming ion, respectively.
Received: 10 April 2002 / Accepted: 7 January 2003
Acknowledgements This work is part of a COFIN project (04 Scienze della Terra, NR 17, 2000) supported by MURST. Dr Dapiaggi is kindly acknowledged
for help during the data collection at the Dipartimento di Scienze della Terra, University of Milan. 相似文献
Regional three-dimensional inversions of teleseismic P-wave travel time residuals recorded by high-frequency regional and local seismic networks operating along the Western Alps and surrounding regions were carried out and lithosphere and upper mantle P-wave velocity models down to 300 km were obtained.
Residuals of more than 500 teleseismic events, recorded by 98 fixed and temporary seismic stations, have been inverted.
The comparison between real residuals and the ones obtained from tomographic model indicates that the method is able to solve the feature of the regional heterogeneities.
Where the resolution is good, coherent lithospheric and upper mantle structures are imaged. In the shallower layers, high- and low-velocity anomalies follow the structural behaviour of the Alpine-Apenninic chains showing the existence of very strong velocity contrasts. In the deepest layers, velocity contrast decreases however two deep-seated high-velocity structures are observed. The most extended in depth and approximately trending NE-SW has been interpreted as a wreck of the oldest subduction responsible of the Alpine orogenesis. The second one, connected to the northwestern sector of the Apenninic chain, appears to vanish at depths greater than 180 km and is probably due to still active Apenninic roots.
Cross-sections depict the spatial trend of perturbations and in particular outline the sub-vertical character of the Alpine and Apenninic anomalies. Under the Ligurian Sea, the 3-D inversion confirms the uplift of the asthenosphere in agreement with the tectonic evolution of the basin. 相似文献
In AD 1826 sealers reported earthquake and tsunami activity in Fiordland, although, contemporary or near‐contemporary accounts of tsunami inundation at the time are elusive. A detailed analysis of recent sediments from Okarito Lagoon builds on contextual evidence provided by earlier research concerning past tsunami inundation. Sedimentological, geochemical, micropalaeontological and geochronological data are used to determine palaeoenvironments before, during and after what was most probably tsunami inundation in AD 1826. The most compelling chronological control is provided fry a young cohort of trees growing on a raised shoreline bench stranded fry a drop in the lagoon water level following tsunami inundation. 相似文献
In Germany, the gasoline additive methyl tert‐butyl ether (MTBE) is almost constantly detected in measurable concentrations in surface waters and is not significantly removed during riverbank filtration. The removal of MTBE from water has been the focus of many studies that mostly were performed at high concentration levels and centred in understanding the mechanisms of elimination. In order to assess the performance of conventional and advanced water treatment technologies for MTBE removal in the low concentration range further studies were undertaken. Laboratory experiments included aeration, granulated activated carbon (GAC) adsorption, ozonation and advanced oxidation processes (AOP). The results show that the removal of MTBE by conventional technologies is not easily achieved. MTBE is only removed by aeration at high expense. Ozonation at neutral pH values did not prove to be effective in eliminating MTBE at all. The use of ozone/H2O2 (AOP) may lead to a partly elimination of MTBE. However, the ozone/H2O2 concentrations required for a complete removal of MTBE from natural waters is much higher than the ozone levels applied nowadays in waterworks. MTBE is only poorly adsorbed on activated carbon, thus GAC filtration is not efficient in eliminating MTBE. A comparison with real‐life data from German waterworks reveals that if MTBE is detected in the raw water it is most often found in the corresponding drinking water as well due to the poor removal efficiency of conventional treatment steps. 相似文献