High-throughput in-situ characterization and modelling of precipitation kinetics in compositionally graded alloys

The development of new engineering alloy chemistries is a time consuming and iterative process. A necessary step is characterization of the nano/microstructure to provide a link between the processing and properties of each alloy chemistry considered. One approach to accelerate the identification of optimal chemistries is to use samples containing a gradient in composition, ie. combinatorial samples, and to investigate many different chemistries at the same time. However, for engineering alloys, the final properties depend not only on chemistry but also on the path of microstructure development which necessitates characterization of microstructure evolution for each chemistry. In this contribution we demonstrate an approach that allows for the in-situ, nanoscale characterization of the precipitate structures in alloys, as a function of aging time, in combinatorial samples containing a composition gradient. The approach uses small angle x-ray scattering (SAXS) at a synchrotron beamline. The Cu-Co system is used for the proof-of-concept and the combinatorial samples prepared contain a gradient in Co from 0% to 2%. These samples are aged at temperatures between 450{\textdegree}C and 550{\textdegree}C and the precipitate structures (precipitate size, volume fraction and number density) all along the composition gradient are simultaneously monitored as a function of time. This large dataset is used to test the applicability and robustness of a conventional class model for precipitation that considers concurrent nucleation, growth and coarsening and the ability of the model to describe such a large dataset.Comment: Published in Acta Materiali

An assessment of global resources of rocks as suitable raw materials for carbon capture and storage by mineralisation

Carbon capture and storage by mineralisation (CCSM) is a method proposed for capturing CO2 by reacting it with magnesium in ultramafic rocks to form carbonate minerals and silica. Large quantities of magnesium silicate rocks are required for this process and to demonstrate the feasibility, and adequately plan for the development and supply of mineral resources, their locations and quantities must be known. This study attempts to globally define the spatial extent and quantity of resources that could be used for the CCSM processes and to assess, if based on resources, this could be a viable, widely applicable CO2 sequestration process. It has been estimated that around 90 teratonnes of material is available. This is sufficient to capture global CO2 emissions for over 700 years at current levels of output and highlights the enormous resource. Even if only a small part is utilised, it could make a significant impact on CO2 reduction. The majority of the resource is contained within ophiolitic rocks. The study further attempts to split CCSM resources into altered (serpentine-rich rocks) and unaltered (olivine-rich rocks) due to the different processing requirements for these rock types. Carbon capture and storage by mineralisation is likely to be of most use in areas with no access to underground geological CO2 storage or for small operations where underground storage is not practical. This study demonstrates that substantial resources are available and their supply is unlikely to be a constraint

Spherical solid-propellant rocket motor Patent

Spherical solid propellant rocket engine desig

Geodynamic setting and origin of the Oman/UAE ophiolite

The ~500km-long mid-Cretaceous Semail nappe of the Sultanate of Oman and UAE (henceforth referred to as the Oman ophiolite) is the largest and best-preserved ophiolite complex known. It is of particular importance because it is generally believed to have an internal structure and composition closely comparable to that of crust formed at the present-day East Pacific Rise (EPR), making it our only known on-land analogue for ocean lithosphere formed at a fast spreading rate. On the basis of this assumption Oman has long played a pivotal role in guiding our conceptual understanding of fast-spreading ridge processes, as modern fast-spread ocean crust is largely inaccessible

Evidence for dissolution-reprecipitation of apatite and preferential LREE mobility in carbonatite-derived late-stage hydrothermal processes

The Tundulu and Kangankunde carbonatite complexes in the Chilwa Alkaline Province, Malawi, contain late-stage, apatite-rich lithologies termed quartz-apatite rocks. Apatite in these rocks can reach up to 90 modal% and displays a distinctive texture of turbid cores and euhedral rims. Previous studies of the paragenesis and rare earth element (REE) content of the apatite suggest that heavy REE (HREE)-enrichment occurred during the late-stages of crystallization. This is a highly unusual occurrence in intrusions that are otherwise light REE (LREE) enriched. In this contribution, the paragenesis and formation of the quartz-apatite rocks from each intrusion is investigated and re-evaluated, supported by new electron microprobe (EPMA) and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) data to better understand the mechanism of HREE enrichment. In contrast to the previous work at Tundulu, we recognize three separate stages of apatite formation, comprising an “original” euhedral apatite, “turbid” apatite, and “overgrowths” of euhedral late apatite. The crystallization of synchysite-(Ce) is interpreted to have occurred subsequent to all phases of apatite crystallization. The REE concentrations and distributions in the different minerals vary, but generally higher REE contents are found in later-stage apatite generations. These generations are also more LREE-enriched, relative to apatite that formed earlier. A similar pattern of increasing LREE-enrichment and increased REE concentrations toward later stages of the paragenetic sequence is observed at Kangankunde, where two generations of apatite are observed, the second showing higher REE concentrations, and relatively higher LREE contents. The changing REE distribution in the apatite, from early to late in the paragenetic sequence, is interpreted to be caused by a combination of dissolution-reprecipitation of the original apatite and the preferential transport of the LREE complexes by F- and Cl-bearing hydrothermal fluids. Successive pulses of these fluids transport the LREE out of the original apatite, preferentially re-precipitating it on the rim. Some LREE remained in solution, precipitating later in the paragenetic sequence, as synchysite-(Ce). The presence of F is supported by the F content of the apatites, and presence of REE-fluorcarbonates. Cl is not detected in the apatite structure, but the role of Cl is suggested from comparison with apatite dissolution experiments, where CaCl2 or NaCl cause the reprecipitation of apatite without associated monazite. This study implies that, despite the typically LREE enriched nature of carbonatites, significant degrees of hydrothermal alteration can lead to certain phases becoming residually enriched in the HREE. Although at Tundulu the LREE-bearing products are re-precipitated relatively close to the REE source, it is possible that extensive hydrothermal activity in other carbonatite complexes could lead to significant, late-stage fractionation of the REE and the formation of HREE minerals. Keywords: Apatite, carbonatite, rare earth elements, Chilwa Alkaline Province, Tundulu, Kangankunde, REE mobility, dissolution-reprecipitatio

A Cahn-Hilliard-Darcy model for tumour growth with chemotaxis and active transport

Using basic thermodynamical principles we derive a Cahn--Hilliard--Darcy model for tumour growth including nutrient diffusion, chemotaxis, active transport, adhesion, apoptosis and proliferation. The model generalise earlier models and in particular include active transport mechanisms which ensures thermodynamical consistency. We perform a formally matched asymptotic expansion and develop several sharp interface models. Some of them are classical and some new ones which for example include a jump in the nutrient density at the interface. A linear stability analysis for a growing nucleus is performed and in particular the role of the new active transport term is analysed. Numerical computations are performed to study the influence of the active transport term for specific growth scenarios

UK export performance research - review and implications

Previous research on export performance has been criticized for being a mosaic of autonomous endeavours and for a lack of theoretical development. Building upon extant models of export performance, and a review and analysis of research on export performance in the UK for the period 1990-2005, an integrated model of export performance is developed and theoretical explanations of export performance are put forward. It is suggested that a multi-theory approach to explaining export performance is viable. Management and policy implications for the UK emerging from the review and synthesis of the literature and the integrated model are discussed