POWTEX Neutron Diffractometer at FRM II - new perspectives for in-situ rock deformation analysis

EGU2012-13521 In Geoscience quantitative texture analysis here defined as the quantitative analysis of the crystallographic preferred orientation (CPO), is a common tool for the investigation of fabric development in mono- and polyphase rocks, their deformation histories and kinematics. Bulk texture measurements also allow the quantitative characterisation of the anisotropic physical properties of rock materials. A routine tool to measure bulk sample volumes is neutron texture diffraction, as neutrons have large penetration capabilities of several cm in geological sample materials. The new POWTEX (POWder and TEXture) Diffractometer at the neutron research reactor FRM II in Garching, Germany is designed as a high-intensity diffractometer by groups from the RWTH Aachen, Forschungszentrum Jülich and the University of Göttingen. Complementary to existing neutron diffractometers (SKAT at Dubna, Russia; GEM at ISIS, UK; HIPPO at Los Alamos, USA; D20 at ILL, France; and the local STRESS-SPEC and SPODI at FRM II) the layout of POWTEX is focused on fast time-resolved experiments and the measurement of larger sample series as necessary for the study of large scale geological structures. POWTEX is a dedicated beam line for geoscientific research. Effective texture measurements without sample tilting and rotation are possible firstly by utilizing a range of neutron wavelengths simultaneously (Time-of-Flight technique) and secondly by the high detector coverage (9.8 sr) and a high flux (�~1x10 7 n/cm2s) at the sample. Furthermore the instrument and the angular detector resolution is designed also for strong recrystallisation textures as well as for weak textures of polyphase rocks. These instrument characteristics allow in-situ time-resolved texture measurements during deformation experiments on rocksalt, ice and other materials as large sample environments will be implemented at POWTEX. The in-situ deformation apparatus is operated by a uniaxial spindle drive with a maximum axial load of 250 kN, which will be redesigned to minimize shadowing effects inside the cylindrical detector. The HT deformatione experiments will be carried out in uniaxial compression or extension and an upgrade to triaxial deformation conditions is envisaged. The load frame can alternatively be used for ice deformation by inserting a cryostat cell for temperatures down to 77 K with a triaxial apparatus allowing also simple shear experiments on ice. Strain rates range between 10-8 and 10-3 s-1 reaching to at least 50% axial strain. The deformation apparatus is designed for continuous long-term deformation experiments and can be exchanged between in-situ and ex-situ placements during continuous operation inside and outside the neutron detector

Deformation, CPO, and Elastic Anisotropy in Low‐Grade Metamorphic Serpentinites, Atlantis Massif Oceanic Core Complex

Crystallographic preferred orientation (CPO) and the associated seismic anisotropy of serpentinites are important factors for the understanding of tectonic settings involving hydrated Earth´s mantle, for example, at slow-spreading mid-ocean ridges. CPO of lizardite and magnetite in low-grade metamorphic serpentinites from the Atlantis Massif oceanic core complex (Mid-Atlantic Ridge, 30°N) were determined using synchrotron high energy X-ray diffraction in combination with Rietveld texture analysis. Serpentinite mesh structures show weak CPO while deformed samples show a single (0001) maximum perpendicular to the foliation. Seismic anisotropies calculated from CPO show up to >11% anisotropy for compressional waves (Vp) and shear wave splitting up to 0.38 km/s in the deformed samples. This indicates that deformation in shear zones controls elastic anisotropy and highlights its importance in defining the seismic signature of hydrated upper mantle

Strain partitioning across a subduction thrust fault near the deformation front of the Hikurangi subduction margin, New Zealand: A magnetic fabric study on IODP Expedition 375 Site U1518

Understanding the distribution of strain along thrust and splay faults in active accretionary systems is crucial to understand the mechanical properties of the sediments and the strength of the fault zone and its slip behavior. This paper investigates the distribution of strain through sediment compaction and texture development across the Pāpaku fault, a major splay fault near the deformation front of the Hikurangi subduction margin, New Zealand using the anisotropy of magnetic susceptibility technique (AMS). International Ocean Discovery Program Site U1518 penetrated hanging wall, fault zone and footwall sequences to a maximum depth of 484.9 meters below seafloor. A total of 330 discrete samples was subjected to AMS measurements and magnetic remanence data used to reconstruct the axial orientation of each sample in a geographic reference frame. The AMS display distinct fabric differences between hanging wall, through the fault zone and footwall domains, demonstrating that strain is partitioned across the fault zone. Hanging wall sequences show a strike-parallel northeasterly lineation of K$_{max}$ and weakly prolate shapes, typical for a component of northeast-southwest lateral shortening. In contrast, footwall sequences are more oblate and show a clustering of K$_{max}$ in northerly direction. This demonstrates that strain in the footwall is dominated by gravitational loading, however a component of sub-horizontal east-westerly strain, parallel to the convergence direction of the Pacific Plate exists. Strain decoupling between hanging- and footwall sequences occurs near the top of the Pāpaku fault zone. Differences in the degree of magnetic susceptibility between footwall sediments incorporated into the fault zone, and the underlying undeformed footwall sequences are indicative for the progressive dewatering of the underconsolidated footwall sequences

Factors affecting the Faradaic efficiency of Fe(0) electrocoagulation

Electrocoagulation (EC) using Fe(0) electrodes is a low cost water treatment technology that relies on efficient production of Fe(II) from the electrolytic dissolution of Fe(0) electrodes (i.e. a high Faradaic efficiency). However, the (electro)chemical factors that favor Fe(0) oxidation rather than O2 evolution during Fe(0) EC have not been identified. In this study, we combined electrochemical methods, electron microscopy and Fe measurements to systematically examine the interdependent effects of current density (i), anodic interface potential (EA) and solution chemistry on the Faradaic efficiency. We found that Fe(0) oxidation was favored (Faradaic efficiency >0.85) in chloride and bromide solutions at all i, whereas carbonate, phosphate, citrate, and nitrate solutions lead to Faradaic efficiencies <0.1. The anodic reaction (i.e. Fe(0) oxidation or O2 evolution) only depended on i in the sulfate and formate solutions. Experiments in binary-anion solutions revealed that molar ratios of [HCO3−]/[Cl−] near 100 and [NO3−]/[Cl−] near 20 separated the electrochemical domains of Fe(0) oxidation and O2 evolution in the EC system. These molar ratios were supported by experiments in synthetic groundwater solutions. We also found that the EA vs i curves for solutions with poor Faradaic efficiency overlapped but were situated 2–4 V vs Ag/AgCl higher than those of solutions with high Faradaic efficiency. Therefore, the position of the EA vs i curve, rather than the EA alone, can be used to determine unambiguously the reaction occurring on the Fe(0) anode during EC treatment

Crystallographic preferred orientations of exhumed subduction channel rocks from the Eclogite Zone of the Tauern Window (Eastern Alps, Austria), and implications on rock elastic anisotropies at great depths

Highlights • Analysis of crystallographic preferred orientations of high-pressure polymineralic rocks by time-of-flight neutron diffraction • Elastic properties of a complete set of subduction channel rocks calculated from their crystallographic preferred orientation • Vp/Vs ratio and P-wave anisotropy of eclogites and metasediments • Influence of eclogite retrogression during exhumation on their elastic properties • Evaluation of the seismic signature of both clastic and carbonate sediments in subduction channels Abstract Crystallographic preferred orientations (CPO) of rocks from an exhumed subduction channel of the Alpine orogen were determined using time-of-flight neutron diffraction. This method allows the investigation of large polymineralic samples and, more importantly, the application of full pattern fit methods to constrain CPOs of mineralogically complex rocks. Samples studied include intensely deformed fresh and retrogressed eclogites, as well as metasediments, which are interleaved with the eclogites in the subduction channel. From the CPO, seismic properties of the samples were calculated. P- wave anisotropies of the eclogite samples are fairly low, with an average of about 1.5%, and mainly constrained by pronounced omphacite CPO. Growth and deformation of retrograde amphibole in the eclogites also led to a pronounced CPO, which has a large impact on seismic anisotropies by raising them to up to 3.7% and changing the orientations of velocity maxima. Elastic anisotropies of the subducted metasediments are higher (up to 7.4%) and constrained by quartz and mica CPO in clastics and by calcite CPO in marble. VP/VS ratios may help to distinguish fresh eclogites from retrogressed ones, and both rock types from mantle peridotites of downgoing lithospheric slabs in seismic imaging. Our data also indicate that subducted terrigenous sediments are not only strongly anisotropic, but also have low VP/VS ratios. This way there may be potential to image them by seismic tomography at depth in active subduction channels

Homogeneous nucleation of colloidal melts under the influence of shearing fields

We study the effect of shear flow on homogeneous crystal nucleation, using Brownian Dynamics simulations in combination with an umbrella sampling like technique. The symmetry breaking due to shear results in anisotropic radial distribution functions. The homogeneous shear rate suppresses crystal nucleation and leads to an increase of the size of the critical nucleus. These observations can be described by a simple, phenomenological extension of classical nucleation theory. In addition, we find that nuclei have a preferential orientation with respect to the direction of shear. On average the longest dimension of a nucleus is along the vorticity direction, while the shortest dimension is preferably perpendicular to that and slightly tilted with respect to the gradient direction.Comment: 10 pages, 8 figures, Submitted to J. Phys.: Condens. Matte

Organic-Silica Interactions in Saline:Elucidating the Structural Influence of Calcium in Low-Salinity Enhanced Oil Recovery

Abstract Enhanced oil recovery using low-salinity solutions to sweep sandstone reservoirs is a widely-practiced strategy. The mechanisms governing this remain unresolved. Here, we elucidate the role of Ca2+ by combining chemical force microscopy (CFM) and molecular dynamics (MD) simulations. We probe the influence of electrolyte composition and concentration on the adsorption of a representative molecule, positively-charged alkylammonium, at the aqueous electrolyte/silica interface, for four electrolytes: NaCl, KCl, MgCl2, and CaCl2. CFM reveals stronger adhesion on silica in CaCl2 compared with the other electrolytes, and shows a concentration-dependent adhesion not observed for the other electrolytes. Using MD simulations, we model the electrolytes at a negatively-charged amorphous silica substrate and predict the adsorption of methylammonium. Our simulations reveal four classes of surface adsorption site, where the prevalence of these sites depends only on CaCl2 concentration. The sites relevant to strong adhesion feature the O− silica site and Ca2+ in the presence of associated Cl−, which gain prevalence at higher CaCl2 concentration. Our simulations also predict the adhesion force profile to be distinct for CaCl2 compared with the other electrolytes. Together, these analyses explain our experimental data. Our findings indicate in general how silica wettability may be manipulated by electrolyte concentration