230 research outputs found

    Resonance assignments of the microtubule-binding domain of the C. elegans spindle and kinetochore-associated protein 1

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    During mitosis, kinetochores coordinate the attachment of centromeric DNA to the dynamic plus ends of microtubules, which is hypothesized to pull sister chromatids toward opposing poles of the mitotic spindle. The outer kinetochore Ndc80 complex acts synergistically with the Ska (spindle and kinetochore-associated) complex to harness the energy of depolymerizing microtubules and power chromosome movement. The Ska complex is a hexamer consisting of two copies of the proteins Ska1, Ska2 and Ska3, respectively. The C-terminal domain of the spindle and kinetochore-associated protein 1 (Ska1) is the microtubule-binding domain of the Ska complex. We solved the solution structure of the C. elegans microtubule-binding domain (MTBD) of the protein Ska1 using NMR spectroscopy. Here, we report the resonance assignments of the MTBD of C. elegans Ska1.Austrian Science Fund (project P22170, and the doctoral school ‘‘DK Molecular Enzymology’’ (W901-B05)

    Sustainable infrastructure development through use of calcined excavated waste clay as a supplementary cementitious material

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    Major infrastructure development projects in London produce large quantities of London clay and use significant volumes of concrete. Portland cement (CEM I) in concrete is normally partially replaced by supplementary cementitious materials such as ground granulated blastfurnace slag or pulverised fuel ash. The supply of supplementary cementitious materials is critical to the production of sustainable concrete. This study has investigated use of waste London clay as a supplementary cementitious material. The optimum calcined clay was produced at 900 °C and concrete made with 30 wt% of CEM I replaced by calcined clay had 28-day strengths greater than control samples. Compressive strengths of concrete containing calcined London clay were similar to concrete containing ground granulated blastfurnace slag and pulverised fuel ash. The production of calcined London clay emits ∼70 kg CO2/tonne and this is 91% lower than CEM I. 30 wt% replacement of CEM I by calcined London clay therefore produces concrete with ∼27% lower embodied carbon. London clay can be calcined to form a technically viable supplementary cementitious material and use of this in concrete would enable major civil infrastructure projects to contribute to a circular economy

    Use of clay in the manufacture of lightweight aggregate

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    Clay is used as a raw material for the production of lightweight aggregates because it is readily processed into suitable granules and forms low-density but high strength aggregate particles when sintered at relatively low temperatures. The use of waste clay generated by major infrastructure development projects to make lightweight aggregate has a positive environmental impact and contributes towards a more circular economy. This paper reviews the manufacturing process used to produce lightweight aggregates from clay and the influence of processing conditions on properties. It also reviews secondary materials that have been incorporated into clays to produce lightweight aggregates. Additional research is required to improve understanding of the effects of composition and production parameters on the pore structure, density, water adsorption and strength of clay derived lightweight aggregates

    Immobilization of sulfates and heavy metals in gold mine tailings by sodium silicate and hydrated lime

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    Gold mining produces hazardous tailings wastes with elevated sulfur content and high levels of heavy metals including oxyanion elements such as V and As. This research investigated activation of these tailings with calcium hydroxide and sodium hydroxide/sodium silicate as a way to stabilize the material and limit leaching of harmful components. The effects of thermal treatment on the reactivity of the tailings and the use of different activating solutions on the physical properties, microstructure and leaching of harmful components are reported. The effect of adding ground granulated blast furnace slag to the tailings is also assessed. The use of 5 wt % Ca(OH)2 activating solution produces optimum performance increasing the immobilization efficiency of sulfates, arsenic and the other harmful elements. Heat-treating mine tailings at 900 °C slightly improves the reactivity but did not improved the immobilization efficiency. Microstructural analysis by TEM and XRD confirmed that stabilization is based on calcium sulfate and/or ettringite formation during alkali-activation. All materials achieved reasonable compressive strength after 28 days of curing and the potential for using alkali activation as a method to treat tailings from mining is discussed

    Immobilization of sulfates and heavy metals in gold mine tailings by sodium silicate and hydrated lime

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    AbstractGold mining produces hazardous tailings wastes with elevated sulfur content and high levels of heavy metals including oxyanion elements such as V and As. This research investigated activation of these tailings with calcium hydroxide and sodium hydroxide/sodium silicate as a way to stabilize the material and limit leaching of harmful components. The effects of thermal treatment on the reactivity of the tailings and the use of different activating solutions on the physical properties, microstructure and leaching of harmful components are reported. The effect of adding ground granulated blast furnace slag to the tailings is also assessed. The use of 5 wt % Ca(OH)₂ activating solution produces optimum performance increasing the immobilization efficiency of sulfates, arsenic and the other harmful elements. Heat-treating mine tailings at 900 °C slightly improves the reactivity but did not improved the immobilization efficiency. Microstructural analysis by TEM and XRD confirmed that stabilization is based on calcium sulfate and/or ettringite formation during alkali-activation. All materials achieved reasonable compressive strength after 28 days of curing and the potential for using alkali activation as a method to treat tailings from mining is discussed.Abstract Gold mining produces hazardous tailings wastes with elevated sulfur content and high levels of heavy metals including oxyanion elements such as V and As. This research investigated activation of these tailings with calcium hydroxide and sodium hydroxide/sodium silicate as a way to stabilize the material and limit leaching of harmful components. The effects of thermal treatment on the reactivity of the tailings and the use of different activating solutions on the physical properties, microstructure and leaching of harmful components are reported. The effect of adding ground granulated blast furnace slag to the tailings is also assessed. The use of 5 wt % Ca(OH)₂ activating solution produces optimum performance increasing the immobilization efficiency of sulfates, arsenic and the other harmful elements. Heat-treating mine tailings at 900 °C slightly improves the reactivity but did not improved the immobilization efficiency. Microstructural analysis by TEM and XRD confirmed that stabilization is based on calcium sulfate and/or ettringite formation during alkali-activation. All materials achieved reasonable compressive strength after 28 days of curing and the potential for using alkali activation as a method to treat tailings from mining is discussed

    Manufacture and performance of lightweight aggregate from waste drill cuttings

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    This research investigated the technical feasibility of transforming waste drill cuttings into lightweight aggregate. Drill cuttings produced from the North Sea oil field were dried, ball milled, formed into pellets and fired at temperatures between 1160 and 1190 °C. Physical properties of the manufactured lightweight aggregate, including particle density, water absorption and compressive strength, were determined. The drill cuttings had a typical evaporite composition containing high concentrations of chloride salts. This limits the potential for using the as-received drill cutting samples in lightweight aggregate production as the products formed show high levels of leaching. The addition of a washing pre-treatment to reduce the leaching of chloride ions was necessary. Washing also reduced the initial sintering temperature and improved lightweight aggregate properties. Sintering at 1180 °C produced lightweight aggregate with particle density of 1.29 g/cm³, water absorption of 3.6% and compressive strengths of 4.4 MPa. The research showed that lightweight aggregate manufacturing represents a resource efficient option for the reuse of waste drill cuttings and provides significant material saving and landfill diversion

    Separating Proactive Conservation from Species Listing Decisions

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    Proactive Conservation is a paradigm of natural resource management in the United States that encourages voluntary, collaborative efforts to restore species before they need to be protected through government regulations. This paradigm is widely used to conserve at-risk species today, and when used in conjunction with the Policy for Evaluation of Conservation Efforts (PECE), it allows for successful conservation actions to preclude listing of species under the Endangered Species Act (ESA). Despite the popularity of this paradigm, and recent flagship examples of its use (e.g., greater sage grouse, Centrocercus urophasianus), critical assessments of the outcomes of Proactive Conservation are lacking from the standpoint of species status and recovery metrics. Here, we provide such an evaluation, using the New England cottontail (Sylvilagus transitionalis), heralded as a success of Proactive Conservation efforts in the northeastern United States, as a case study. We review the history and current status of the species, based on the state of the science, in the context of the Conservation Initiative, and the 2015 PECE decision not to the list the species under the ESA. In addition to the impacts of the PECE decision on the New England cottontail conservation specifically, our review also evaluates the benefits and limits of the Proactive Conservation paradigm more broadly, and we make recommendations for its role in relation to ESA implementation for the future of at-risk species management. We find that the status and assurances for recovery under the PECE policy, presented at the time of the New England cottontail listing decision, were overly optimistic, and the status of the species has worsened in subsequent years. We suggest that use of PECE to avoid listing may occur because of the perception of the ESA as a punitive law and a misconception that it is a failure, although very few listed species have gone extinct. Redefining recovery to decouple it from delisting and instead link it to probability of persistence under recommended conservation measures would remove some of the stigma of listing, and it would strengthen the role of Species Status Assessments in endangered species conservation

    Preparation and characterization of binary Mg-silicate glasses via Sol-Gel route

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    AbstractSol-gel processing allows synthesis of low-energy glasses. In this work, binary magnesium silicate glasses with various MgO contents are synthesized using a modified sol-gel route. TGA and XRD analyses indicate that amorphous glasses with up to 50 mol% MgO can be obtained at 500°C. The reactivity of the glasses is evaluated to assess the use of the sol-gel technique in the large-scale synthesis of alternative cementitious materials. Reactivity tests show that, as MgO content increases, reactivity of glasses increases, reaches an optimum and then declines. This trend doesn’t agree with the theoretical one estimated by NBO/T value, which is generally used for the evaluation of glass reactivity. Mg²⁺ ions play a role as the network modifier when first introduced to silicate glasses. This leads to the depolymerization of the networks, causing an increase in reactivity. Then the magnesium partly behaves as a network former, bonding with oxygens to form MgOₓ polyhedron when there are insufficient primary glass-forming oxide SiO₂, resulting in the polymerization of networks, hence the decrease in reactivity.Abstract Sol-gel processing allows synthesis of low-energy glasses. In this work, binary magnesium silicate glasses with various MgO contents are synthesized using a modified sol-gel route. TGA and XRD analyses indicate that amorphous glasses with up to 50 mol% MgO can be obtained at 500°C. The reactivity of the glasses is evaluated to assess the use of the sol-gel technique in the large-scale synthesis of alternative cementitious materials. Reactivity tests show that, as MgO content increases, reactivity of glasses increases, reaches an optimum and then declines. This trend doesn’t agree with the theoretical one estimated by NBO/T value, which is generally used for the evaluation of glass reactivity. Mg²⁺ ions play a role as the network modifier when first introduced to silicate glasses. This leads to the depolymerization of the networks, causing an increase in reactivity. Then the magnesium partly behaves as a network former, bonding with oxygens to form MgOₓ polyhedron when there are insufficient primary glass-forming oxide SiO₂, resulting in the polymerization of networks, hence the decrease in reactivity

    Acid activated smectite clay as pozzolanic supplementary cementitious material

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    This research has investigated the structural changes and pozzolanic activity produced in acid activated smectite clay. The activation treatment used HCl at different concentrations, using different times and at a range of temperatures. X-ray diffraction, Fourier transform infrared spectroscopy and scanning electron microscopy coupled with energy dispersive X-ray spectroscopy were used to determine the acid dissolution mechanism and characterise the activated clay mineral structure. Acid activation causes dehydroxylation of smectite clay, followed by leaching of octahedral cations. This results in the formation of a silica-rich amorphous phase that exhibits substantial pozzolanic activity compared to the same clay sample that had undergone calcining treatment at 850. The optimum sample was activated for 8 h using 5 M HCl at 90 °C. This was 93 % amorphous. Mortar prisms prepared with 25 % replacement of Portland cement by acid activated smectite produced 93 % compressive strength of plain Portland cement mortar
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