15 research outputs found

    Postaragonite phases of CaCO3 at lower mantle pressures

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    The stability, structure and properties of carbonate minerals at lower mantle conditions has significant impact on our understanding of the global carbon cycle and the composition of the interior of the Earth. In recent years, there has been significant interest in the behavior of carbonates at lower mantle conditions, specifically in their carbon hybridization, which has relevance for the storage of carbon within the deep mantle. Using high-pressure synchrotron X-ray diffraction in a diamond anvil cell coupled with direct laser heating of CaCO3 using a CO2 laser, we identify a crystalline phase of the material above 40 GPa − corresponding to a lower mantle depth of around 1,000 km − which has first been predicted by ab initio structure predictions. The observed sp2 carbon hybridized species at 40 GPa is monoclinic with P21/c symmetry and is stable up to 50 GPa, above which it transforms into a structure which cannot be indexed by existing known phases. A combination of ab initio random structure search (AIRSS) and quasi-harmonic approximation (QHA) calculations are used to re-explore the relative phase stabilities of the rich phase diagram of CaCO3. Nudged elastic band (NEB) calculations are used to investigate the reaction mechanisms between relevant crystal phases of CaCO3 and we postulate that the mineral is capable of undergoing sp2-sp3 hybridization change purely in the P21/c structure − forgoing the accepted post-aragonite Pmmn structure

    Formulation, characterisation and stabilisation of buccal films for paediatric drug delivery of omeprazole

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    This study aimed to develop films for potential delivery of omeprazole (OME) via the buccal mucosa of paediatric patients. Films were prepared using hydroxypropylmethylcellulose (HPMC), methylcellulose (MC), sodium alginate (SA), carrageenan (CA) and metolose (MET) with polyethylene glycol (PEG 400) as plasticiser, OME (model drug) and L-arg (stabiliser). Gels (1% w/w) were prepared at 40°C using water and ethanol with PEG 400 (0–1% w/w) and dried in an oven (40°C). Optimised formulations containing OME and L-arg (1:1, 1:2 and 1:3) were prepared to investigate the stabilisation of the drug. Tensile properties (Texture analysis, TA), physical form (differential scanning calorimetry, DSC; X-ray diffraction, XRD; thermogravimetric analysis, TGA) and surface topography (scanning electron microscopy, SEM) were investigated. Based on the TA results, SA and MET films were chosen for OME loading and stabilisation studies as they showed a good balance between flexibility and toughness. Plasticised MET films were uniform and smooth whilst unplasticised films demonstrated rough lumpy surfaces. SA films prepared from aqueous gels showed some lumps on the surface, whereas SA films prepared from ethanolic gels were smooth and uniform. Drug-loaded gels showed that OME was unstable and therefore required addition of L-arg. The DSC and XRD suggested molecular dispersion of drug within the polymeric matrix. Plasticised (0.5% w/w PEG 400) MET films prepared from ethanolic (20% v/v) gels and containing OME: L-arg 1:2 showed the most ideal characteristics (transparency, ease of peeling and flexibility) and was selected for further investigation

    Rheology of colloidal particles in lyotropic hexagonal liquid crystals: the role of particle loading, shape, and phase transition kinetics

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    The rheology of self-assembled elongated iron oxyhydroxide (FeOOH) and spherical silica (SiO2) particles in hexagonal (H1) liquid crystal (LC) phase of water and non-ionic surfactant C12E9 is investigated by varying particle concentration and cooling rate. The rheology data shows that both SiO2/H1 and FeOOH/ H1 LC composites exhibit a higher G′ when compared to the particle-free H1 phase, with increasing particle loading and cooling rate. FeOOH particles improve G′ of the H1 phase more significantly than SiO2 particles due to the formation of an interconnected network at H1 domain boundaries at cooling rates of 1 and 2 ∘C/min. We hypothesize that self-assembly of particles at domain boundaries leads to a decreased mobility of defects causing an increase in elasticity of particle-laden H1 phase. Dynamic strain sweep and creep experiments show a non-linear stress–strain relationship attributed to the alignment of micellar cylindrical rods under shear.by Siddharth Kulkarni and Prachi Tharej

    Decline of the World’s Saline Lakes

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    Many of the world\u27s saline lakes are shrinking at alarming rates, reducing waterbird habitat and economic benefits while threatening human health. Saline lakes are long-term basin-wide integrators of climatic conditions that shrink and grow with natural climatic variation. In contrast, water withdrawals for human use exert a sustained reduction in lake inflows and levels. Quantifying the relative contributions of natural variability and human impacts to lake inflows is needed to preserve these lakes. With a credible water balance, causes of lake decline from water diversions or climate variability can be identified and the inflow needed to maintain lake health can be defined. Without a water balance, natural variability can be an excuse for inaction. Here we describe the decline of several of the world\u27s large saline lakes and use a water balance for Great Salt Lake (USA) to demonstrate that consumptive water use rather than long-term climate change has greatly reduced its size. The inflow needed to maintain bird habitat, support lake-related industries and prevent dust storms that threaten human health and agriculture can be identified and provides the information to evaluate the difficult tradeoffs between direct benefits of consumptive water use and ecosystem services provided by saline lakes
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