CO2 sequestration by magnesite mineralisation through interaction of Mg-brine and CO2: integrated laboratory experiments and computerised geochemical modelling

ABSTRACT

Several Carbon Capture and Storage (CCS) techniques have been studied including injections of carbon dioxide (CO₂) into the mature and/or depleted hydrocarbon reservoirs and deep saline aquifers. This work aims to test storing CO₂ into the magnesium-rich evaporite strata and also into the stratigraphic intervals containing Mg-rich brines. The test simulates Mg-carbonation of the synthetic solution obtained from the Mg-evaporite mineral, bischofite – both experimentally in the laboratory condition and also through computerised geochemical simulation. The laboratory experiments, which resulted in the crystallisation of anhydrous magnesite, were analysed. The TOUGHREACT^TM, Geochemist’s Workbench^TM (GWB) and PHREEQC^TM software simulated the experiments as computerised geochemical model and tested the results for natural geological conditions. The geochemical simulations successfully demonstrate the immense CCS potential for the Mg-evaporite (as well as the sedimentary strata charged with Mg-evaporitic brine) at their subsurface geological occurrences at elevated pressure-temperature and high salinity.     

Smelting Process of Chromite Ore Fines to Produce Crude Fe–Cr–Ni–N Alloy

Transactions of the Indian Institute of Metals - The smelting behavior of waste chromite ore fines containing Cr and Ni to produce crude Fe–Cr–Ni–N alloy was investigated in this...     

A tamper detection suitable fragile watermarking scheme based on novel payload embedding strategy

Multimedia Tools and Applications - Intentional tampering in digital image content is one of the common malpractices in the current digital arena. So in this paper, the authors have proposed a...     

Hybrid anion exchanger for trace phosphate removal from water and wastewater

Throughout recent decades, the wastewater treatment industry has identified the discharge of nutrients, including phosphates and nitrates, into waterways as a risk to natural environments due to the serious effects of eutrophication. For this reason, new tertiary treatment processes have abounded; these processes generally utilize physico-chemical and biological methods to remove nutrients from secondary wastewaters. The disadvantages of such methods involve larger reactor volumes, operating costs, and waste sludge production; furthermore, complete nutrient removal is unattainable due to thermodynamic and kinetic limitations. The subject study presents the development and performance of a new phosphate-selective sorbent, referred to as hybrid anion exchanger or HAIX. HAIX combines durability and mechanical strength of polymeric anion exchange resins with high sorption affinity of hydrated ferric oxide (HFO) toward phosphate. HAIX is essentially a polymeric anion exchanger within which HFO nanoparticles have been dispersed irreversibly. Laboratory studies show that HAIX selectively removes phosphate from the background of much higher concentrations of competing sulfate, chloride and bicarbonate anions due to the combined presence of Coulombic and Lewis acid-base interactions. Experimental results demonstrate that HAIX's phosphate-sulfate separation factor is over two orders of magnitude greater than that of currently available commercial ion exchange resins. Additionally, optimal HAIX performance occurs at typical secondary wastewater pH conditions i.e., around 7.5. HAIX is amenable to efficient regeneration and reuse with no noticeable loss in capacity.     

Image retrieval based on non-uniform bins of color histogram and dual tree complex wavelet transform

Multimedia Tools and Applications - Traditional Content-Based Image Retrieval (CBIR) systems were developed for retrieving similar kinds of images from a whole image database based on the given...     

Determination of trace perchlorate in high-salinity water samples by ion chromatography with on-line preconcentration and preelution

A simple, automated system for the determination of trace perchlorate by ion chromatography (IC) with an online preconcentration technique is reported. The sample is preconcentrated, and less strongly held ions preeluted before the analyte is transferred to the principal separation system. This approach provides low limits of detection (LOD) and is particularly robust toward the effect of high concentrations of common anions, such as those present in groundwater samples. It compares favorably with currently promulgated EPA method 314.0. The LOD (S/N = 3) is 0.77 microg/L for a 2-mL reagent water sample and decreases more-or-less proportionately with increasing sample volume, at least up to 20 mL. Even with a sample of conductivity 14.7 mS/cm (approximately that of 0.1 M Na2SO4), the recovery of added perchlorate at the 25.0 microg/L level was still 92%. The concentration of added perchlorate in the range of 1-400 microg/L was linearly correlated to the peak area, with an r2 value of 0.9997. The recovery of perchlorate from artificial samples with different conductivity by the present method compares favorably with those from the currently recommended EPA Method. The ability of this approach to remove matrix interferences suggests that it would be also promising for perchlorate analysis in other challenging samples.     

High ferromagnetic transition temperature in PbS and PbS:Mn nanowires

Spontaneous magnetization measured in the temperature range 5-300 K with high ferromagnetic transition temperature (T(c)) has been observed in both undoped and Mn doped (2-8 mol %) PbS nanowires (diameter 30 nm) in polymer. For undoped sample, we find T(c) ~ 290 K while for doped samples T(c) varies between 310-340 K depending on Mn concentrations. Both T(c) and coercive fields are critically dependent on Mn concentrations. Coercive fields show a T(0.5) dependence with temperature for a moderate concentration of Mn (4 mol %) in PbS while it deviates from T(0.5) behavior for higher Mn concentrations. Anionic defects arising out of nonstoichiometric growth is solely responsible for the observed magnetism in undoped PbS nanowires. The role of intrinsic strain along with reduced dimensionality in determining such high T(c) and overall magnetizations has been discussed.     

Macro-to-micro porous special bioactive glass and ceftriaxone-sulbactam composite drug delivery system for treatment of chronic osteomyelitis: an investigation through in vitro and in vivo animal trial

A systematic and extensive approach incorporating in vitro and in vivo experimentation to treat chronic osteomyelitis in animal model were made using antibiotic loaded special bioactive glass porous scaffolds. After thorough characterization for porosity, distribution, surface charge, a novel drug composite were infiltrated by using vacuum infiltration and freeze-drying method which was subsequently analyzed by SEM-EDAX and studied for in vitro drug elution in PBS and SBF. Osteomyelitis in rabbit was induced by inoculation of Staphylococcus aureus and optimum drug-scaffold were checked for its efficacy over control and parenteral treated animals in terms of histopathology, radiology, in vivo drug concentration in bone and serum and implant-bone interface by SEM. It was optimized that 60P samples with 60-65% porosity (bimodal distribution of macro- to micropore) with average pore size ~60 μm and higher interconnectivity, moderately high antibiotic adsorption efficiency (~49%) was ideal. Results after 42 days showed antibiotic released higher than MIC against S. aureus compared to parenteral treatment (2 injections a day for 6 weeks). In vivo drug pharmacokinetics and SEM on bone-defect interface proved superiority of CFS loaded porous bioactive glass implants over parenteral group based on infection eradication and new bone formation.     

ATP depletion blocks herpes simplex virus DNA packaging and capsid maturation

During herpes simplex virus (HSV) assembly, immature procapsids must expel their internal scaffold proteins, transform their outer shell to form mature polyhedrons, and become packaged with the viral double-stranded (ds) DNA genome. A large number of virally encoded proteins are required for successful completion of these events, but their molecular roles are poorly understood. By analogy with the dsDNA bacteriophage we reasoned that HSV DNA packaging might be an ATP-requiring process and tested this hypothesis by adding an ATP depletion cocktail to cells accumulating unpackaged procapsids due to the presence of a temperature-sensitive lesion in the HSV maturational protease UL26. Following return to permissive temperature, HSV capsids were found to be unable to package DNA, suggesting that this process is indeed ATP dependent. Surprisingly, however, the display of epitopes indicative of capsid maturation was also inhibited. We conclude that either formation of these epitopes directly requires ATP or capsid maturation is normally arrested by a proofreading mechanism until DNA packaging has been successfully completed.