Simulations of a coupled hydro-chemo-mechanical system in rocks

A coupled hydro-chemo-mechanical numerical model is developed for these coupled phenomena in many engineering fields. The model has been applied to predicting the response of a stressed rockmass column to an injected reactive fluid (reagent) flow. The response includes evolutions of porosity, permeability, reagent and mineral concentrations during dissolution. In the model, the progress of dissolution is defined by the change in porosity ratio and the porosity increases with dissolution assuming there is no precipitation. The numerical evolutions of porosity, permeability, reagent and mineral concentrations during dissolution are validated against steady state solutions. The model results show that these evolutions are regulated to a certain extent by the applied external loadings: an applied extensional stress enhances the progress of the dissolution process while an applied compression stress slows the progress of the dissolution process. This revised version was published online in July 2006 with corrections to the Cover Date.     

Effet du vieillissement des céramiques poreuses sur leur capacité à évaluer la concentration de pesticide en solution

The soil solution sampling by ceramic cups allows pesticide transfer monitoring in the soil during long times. The ageing of material involves a bias in the sampling results. In laboratory, the comparison of two types of ceramic suction cups, new and installed in situ during four years, shows a modification of the hydrodynamic properties and a possible evolution of the adsorption capacity of the matrix. The passage rate, as well qualitative as quantitative, is better for the old material. Recommendations about site management are finally exposed. To cite this article: N. Domange et al., C. R. Geoscience 336 (2004).     

聚合物溶液在地下连续墙施工中的试验研究

简要叙述了一种新型地下连续墙施工稳定液——聚合物溶液的研制及其与细分散泥浆性能的对比，这种新型聚合物溶液克服了目前使用的地下连续墙稳定液品种单一、性能较差的缺点，满足复杂地层的地下连续墙施工需要。同时阐述了这种稳定液的组成成分和性能及其主要特点。     

Seismic activity at the MCT in Sikkim Himalaya

A microearthquake survey in the Sikkim Himalaya raised a question whether the north–south segment of the Main Central Thrust (MCT) in this part of the Himalaya is seismically active(?). Fault-plane solution of a cluster of events occurred below this segment of the MCT shows right-lateral strike-slip motion. The seismic observations and the geological evidences suggest that a NNE–SSW trending strike-slip fault, beneath this segment, caused right lateral movement on the MCT, and is seismically active.     

Erratic judgements: re-evaluating solutional erosion rates of limestones using erratic-pedestal sites, including Norber, Yorkshire

The re-interpretation of surface karst landforms in Northern England has led to a re-examination of well-known erratic-pedestal sites that were the origin for karst denudation rates applied extensively, on the supposition that erratics protect underlying limestone from rainwater solution. Height of the pedestal has been used to calculate long-term solutional-lowering, as much as 50 cm in 15 ka (33.3 mm/ka) from UK sites. The sites include Norber and Scar Close, Yorkshire, UK. This paper shows that the sites have been misinterpreted, in particular at Norber where the erratics lie on a pre-existing structurally stepped surface. Norber and several other sites also experience much mechanical weathering, in relatively weak, well-fractured limestones, a process which must be distinguished from solution. Sites in strong, less-fractured limestones demonstrate lower rates, which are sounder indications of land surface lowering. Some pedestals have been confirmed as partly resulting from solutional weathering in surrounding soil and vegetation. Re-evaluation reduces solution rates to 3–13 cm in 15 ka. Applying such rates has profound implications for understanding limestone landscapes, challenging orthodox views.     

Case study on the strategy and application of enhancement solutions to improve remediation of soils contaminated with Cu, Pb and Zn by means of electrodialysis

Numerous studies have been conducted with electrochemical removal of heavy metals from spiked kaolinite. Meanwhile, when moving from kaolinite to real soils, new factors must be taken into account—factors influencing, e.g., the buffering capacity of the soil against acidification and the adsorption/desorption processes of the heavy metals. The present study gives some examples where it is necessary to use an enhancement solution to aid desorption of Cu, Zn and Pb during electrodialytic treatment. Dependent on the composition of the pollution, different choices can be made. In the case of a Cu-polluted calcareous soil, ammonia may be used as enhancement solution, due to the formation of charged complexes between ammonia and Cu. Thus, Cu is mobile at high pH when ammonia is added and Cu can be removed without dissolving the calcareous parts. Zn is also mobilized by ammonia, but to a lesser extent than Cu. In the case of Cu, Zn and Pb at the same time, alkaline ammonium citrate may be a solution. It was shown that this enhancement solution could mobilize these three pollutants, but optimization of concentration and pH of the ammonium citrate is still needed. When choosing a remediation scheme for electrochemical treatment of an actual industrially polluted soil, this scheme must be chosen on basis of characterization of soil and pollution combination.     

浓硫酸钠水溶液中的离子对

不同浓度的Na2SO4水溶液的拉曼光谱显示了SO42-的四个拉曼活性带:980 cm-1处的SO42-的对称伸缩振动模式v1带,1 106 cm-1处的反对称伸缩振动模式v3带,448 cm-1处的变形振动模式v2带和617 cm-1处的变形振动模式v4带。482 cm-1处的肩膀峰是由于NaSO4-离子对的形成对448 cm-1的v2带的影响而形成的SO42-的一个新的振动峰。浓Na2SO4水溶液中,水共享离子对[Na+.H2O.SO42-]-是主要的离子对物种。随着Na2SO4水溶液浓度的增加,Na+和SO42-的相互作用增强,NaSO4-离子对所占的摩尔分数增加。     

Semi‐analytical solution to one‐dimensional consolidation for unsaturated soils with semi‐permeable drainage boundary under time‐dependent loading

This paper presents semi‐analytical solutions to Fredlund and Hasan's one‐dimensional consolidation of unsaturated soils with semi‐permeable drainage boundary under time‐dependent loadings. Two variables are introduced to transform two coupled governing equations of pore‐water and pore‐air pressures into an equivalent set of partial differential equations, which are easily solved by the Laplace transform. The pore‐water pressure, pore‐air pressure and settlement are obtained in the Laplace domain. Crump's method is adopted to perform the inverse Laplace transform in order to obtain semi‐analytical solutions in time domain. It is shown that the present solutions are more general and have a good agreement with the existing solutions from literatures. Furthermore, the current solutions can also be degenerated into conventional solutions to one‐dimensional consolidation of unsaturated soils with homogeneous boundaries. Finally, several numerical examples are provided to illustrate consolidation behavior of unsaturated soils under four types of time‐dependent loadings, including instantaneous loading, ramp loading, exponential loading and sinusoidal loading. Parametric studies are illustrated by variations of pore‐air pressure, pore‐water pressure and settlement at different values of the ratio of air–water permeability coefficient, depth and loading parameters. Copyright © 2017 John Wiley & Sons, Ltd.     

Intergranular diffusion rates from the analysis of garnet surfaces: Implications for metamorphic equilibration

Novel approaches to garnet analysis have been used to assess rates of intergranular diffusion between different matrix phases and garnet porphyroblasts in a regionally metamorphosed staurolite‐mica‐schist from the Barrovian‐type area in Scotland. X‐ray maps and chemical traverses of planar porphyroblast surfaces reveal chemical heterogeneity of the garnet grain boundary linked to the nature of the adjacent matrix phase. The garnet preserves evidence of low temperature retrograde exchange with matrix minerals and diffusion profiles documenting cation movement along the garnet boundaries. Garnet–quartz and garnet–plagioclase boundaries preserve evidence of sluggish Mg, Mn and Fe diffusion at comparable rates to volume diffusion in garnet, whereas diffusion along garnet–biotite interfaces is much more effective. Evidence of particularly slow Al transport, probably coupled to Fe³⁺ exchange, is locally preserved on garnet surfaces adjacent to Fe‐oxide phases. The Ca distribution on the garnet surface shows the most complex behaviour, with long‐wavelength heterogeneities apparently unrelated to the matrix grain boundaries. This implies that the Ca content of garnet is controlled by local availability and is thought likely to reflect disequilibrium established during garnet growth. Geochemical anomalies on the garnet surfaces are also linked to the location of triple junctions between the porphyroblasts and the matrix phases, and imply enhanced transport along these channels. The slow rates of intergranular diffusion and the characteristics of different boundary types may explain many features associated with the prograde growth of garnet porphyroblasts. Thus, minerals such as quartz, Fe‐oxides and plagioclase whose boundaries with garnet are characterized by slow intergranular diffusion rates appear to be preferentially trapped as inclusions within porphyroblasts. As such grain boundary diffusion rates may be a significant kinetic impediment to metamorphic equilibrium and garnet may struggle to maintain chemical and textural equilibrium during growth in pelites.