Interaction of short cracks with the local microstructure

AbstractIncreasing the resistance of a material against fatigue crack growth by optimizing the microstructure is one of the major tasks of modern materials science. Thereby grain and phase boundaries are microstructural elements which can decelerate the propagation rate especially of short cracks. However, in different materials cracks and grain boundaries interact differently. For instance in some steels the blocking effect was only found for large angle grain boundaries while small angle boundaries showed nearly no effect. On the other hand in nickel based superalloys a retardation of cracks was found even for small angle boundaries when the crack was propagating in stage I. Even in front of the same grain boundary, the blocking effect varies for different cracks. To investigate this behaviour systematically focused ion beam (FIB) initiated cracks were used. By this method of artificial crack initiation the crack parameters like crack length and distance to the obstacle can be varied separately. Additionally special grain boundaries can be selected after a microstructural characterisation by electron backscatter diffraction (EBSD). Finally FIB tomography helps to understand the process how a crack overcomes a grain boundary

Ecological Interface Design in Neuro-Critical Care

Neuro-critical care is a data-intensive environment that requires physicians to integrate information across multiple screens, sources, and software. Despite the advances in neuromonitoring techniques, interfaces that allow for viewing and analyzing of historic data are not common. However, historical data is critical to identify patterns important for patient care. Instead, physicians view the trends of a patient’s neurophysiological variables by continuously watching the bedside monitor or they rely on checking the paper (or digital) charts for a patient where variables have been recorded periodically (usually once an hour). In neuro-critical care, physicians need to understand the historic and current state as well as predict the future state of intracranial pressure (ICP). ICP is the most monitored brain-specific physiologic variable in the Intensive Care Unit (ICU) and is considered a biomarker for secondary brain injury. As a result, ICP would benefit greatly from showing key patterns important to patient state and care. The ICU is a stressful, dynamic, and time-sensitive environment where the performance of physicians and their ability to correctly diagnose and manage patient treatment has a significant impact on patient outcomes. Physicians rely on the bedside physiologic monitor to detect changes in physiologic variables. The monitor must provide the information required to understand the patient’s condition so physicians can determine the optimal treatment plan. With the high cognitive demands and complex sociotechnical environment of the ICU, an opportunity exists for improved neuro-critical care monitoring to support physicians’ decision-making. Ecological Interface Design (EID) is an approach to interface design that has proven effective for complex, sociotechnical, real-time, and dynamic systems. Research suggests that an EID approach combined with user-centered design has a positive impact on performance, especially in unfamiliar scenarios. The objective of this research is to explore an EID design approach combined with user-centered design to enhance the bedside physiologic monitor through the addition of visualizations that help support physicians' understanding of complex relationships and concepts in neuro-critical care. The hope is that providing more-advanced visualizations on the bedside physiologic monitor will lead to improved situation awareness, decreased mental workload, and expertise development acceleration of novice clinicians in the neuro-ICU. The work presented in this thesis builds on the Cognitive Work Analysis (CWA) and observations in the ICU already completed by Uereten et al (2020). The design of the visualizations for use on the bedside physiologic monitor was highly iterative and involved the inputs from the CWA and observations as well as ongoing feedback and focus areas provided by Dr. Victoria McCredie, our clinical collaborator and critical care physician at Toronto Western Hospital. The visualizations were evaluated and validated in semi-structured interviews with trainees (fellows) and experts (staff physicians) in neuro-critical care. The semi-structured interviews with trainees were used as a preliminary usability assessment of the visualizations and the interviews with staff physicians were used to iterate and refine the designs. The results from both sets of interviews were used to create a final design prototype that is currently being tested in a usability study with trainee physicians (January-March 2023)

Review of foundational concepts and emerging directions in metamaterial research: Design, phenomena, and applications

In the past two decades, artificial structures known as metamaterials have been found to exhibit extraordinary material properties that enable the unprecedented manipulation of electromagnetic waves, elastic waves, molecules, and particles. Phenomena such as negative refraction, bandgaps, near perfect wave absorption, wave focusing, negative Poissons ratio, negative thermal conductivity, etc., all are possible with these materials. Metamaterials were originally theorized and fabricated in electrodynamics, but research into their applications has expanded into acoustics, thermodynamics, seismology, classical mechanics, and mass transport. In this Research Update we summarize the history, current state of progress, and emerging directions of metamaterials by field, focusing the unifying principles at the foundation of each discipline. We discuss the different designs and mechanisms behind metamaterials as well as the governing equations and effective material parameters for each field. Also, current and potential applications for metamaterials are discussed. Finally, we provide an outlook on future progress in the emerging field of metamaterials.Comment: 22 pages, 3 figures, 1 tabl

Impact of highly basic solutions on sorption of Cs+ to subsurface sediments from the Hanford site, USA

The effect of caustic NaNO3 solutions on the sorption of 137Cs to a Hanford site micaceous subsurface sediment was investigated as a function of base exposure time (up to 168 d), temperature (10°C or 50°C), and NaOH concentration (0.1 mol/L to 3 mol/L). At 10°C and 0.1 M NaOH, the slow evolution of [Al]aq was in stark contrast to the rapid increase and subsequent loss of [Al]aq observed at 50°C (regardless of base concentration). Exposure to 0.1 M NaOH at 10°C for up to 168 d exhibited little if any measurable effect on sediment mineralogy, Cs+ sorption, or Cs+ selectivity; sorption was well described with a two-site ion exchange model modified to include enthalpy effects. At 50°C, dissolution of phyllosilicate minerals increased with [OH]. A zeolite (tetranatrolite; Na2Al2Si3O10·2H2O) precipitated in 0.1 M NaOH after about 7 days, while an unnamed mineral phase (Na14Al12Si13O51·6H2O) precipitated after 4 and 2 days of exposure to 1 M and 3 M NaOH solutions, respectively. Short-term (16 h) Cs+ sorption isotherms (10−9–10−2 mol/L) were measured on sediment after exposure to 0.1 M NaOH for 56, 112, and 168 days at 50°C. There was a trend toward slightly lower conditional equilibrium exchange constants (∆log NaCsKc ~ 0.25) over the entire range of surface coverage, and a slight loss of high affinity sites (15%) after 168 days of pretreatment with 0.1 M base solution. Cs+ sorption to sediment over longer times was also measured at 50°C in the presence of NaOH (0.1 M, 1 M, and 3MNaOH) at Cs+ concentrations selected to probe a range of adsorption densities. Model simulations of Cs+ sorption to the sediment in the presence of 0.1 M NaOH for 112 days slightly under-predicted sorption at the lower Cs+ adsorption densities. At the higher adsorption densities, model simulations under-predicted sorption by 57%. This under-prediction was surmised to be the result of tetranatrolite precipitation, and subsequent slow Na → Cs exchange. At higher OH concentrations, Cs+ sorption in the presence of base for 112 days was unexpectedly equal to, or greater than that expected for pristine sediment. The precipitation of secondary phases, coupled with the fairly unique mica distribution and quantity across all size-fractions in the Hanford sediment, appears to mitigate the impact of base dissolution on Cs+ sorption

Selective Thermal Emission Coatings for Improved Turbine Efficiency

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Impact of highly basic solutions on sorption of Cs+ to subsurface sediments from the Hanford site, USA

The effect of caustic NaNO3 solutions on the sorption of 137Cs to a Hanford site micaceous subsurface sediment was investigated as a function of base exposure time (up to 168 d), temperature (10°C or 50°C), and NaOH concentration (0.1 mol/L to 3 mol/L). At 10°C and 0.1 M NaOH, the slow evolution of [Al]aq was in stark contrast to the rapid increase and subsequent loss of [Al]aq observed at 50°C (regardless of base concentration). Exposure to 0.1 M NaOH at 10°C for up to 168 d exhibited little if any measurable effect on sediment mineralogy, Cs+ sorption, or Cs+ selectivity; sorption was well described with a two-site ion exchange model modified to include enthalpy effects. At 50°C, dissolution of phyllosilicate minerals increased with [OH]. A zeolite (tetranatrolite; Na2Al2Si3O10·2H2O) precipitated in 0.1 M NaOH after about 7 days, while an unnamed mineral phase (Na14Al12Si13O51·6H2O) precipitated after 4 and 2 days of exposure to 1 M and 3 M NaOH solutions, respectively. Short-term (16 h) Cs+ sorption isotherms (10−9–10−2 mol/L) were measured on sediment after exposure to 0.1 M NaOH for 56, 112, and 168 days at 50°C. There was a trend toward slightly lower conditional equilibrium exchange constants (∆log NaCsKc ~ 0.25) over the entire range of surface coverage, and a slight loss of high affinity sites (15%) after 168 days of pretreatment with 0.1 M base solution. Cs+ sorption to sediment over longer times was also measured at 50°C in the presence of NaOH (0.1 M, 1 M, and 3MNaOH) at Cs+ concentrations selected to probe a range of adsorption densities. Model simulations of Cs+ sorption to the sediment in the presence of 0.1 M NaOH for 112 days slightly under-predicted sorption at the lower Cs+ adsorption densities. At the higher adsorption densities, model simulations under-predicted sorption by 57%. This under-prediction was surmised to be the result of tetranatrolite precipitation, and subsequent slow Na → Cs exchange. At higher OH concentrations, Cs+ sorption in the presence of base for 112 days was unexpectedly equal to, or greater than that expected for pristine sediment. The precipitation of secondary phases, coupled with the fairly unique mica distribution and quantity across all size-fractions in the Hanford sediment, appears to mitigate the impact of base dissolution on Cs+ sorption

CO2 Utilization and Storage in Shale Gas Reservoirs: Experimental Results and Economic Impacts

AbstractNatural gas is considered a cleaner and lower-emission fuel than coal, and its high abundance from advanced drilling techniques has positioned natural gas as a major alternative energy source for the U.S. However, each ton of CO2 emitted from any type of fossil fuel combustion will continue to increase global atmospheric concentrations. One unique approach to reducing anthropogenic CO2 emissions involves coupling CO2 based enhanced gas recovery (EGR) operations in depleted shale gas reservoirs with long-term CO2 storage operations. In this paper, we report unique findings about the interactions between important shale minerals and sorbing gases (CH4 and CO2) and associated economic consequences. Where enhanced condensation of CO2 followed by desorption on clay surface is observed under supercritical conditions, a linear sorption profile emerges for CH4. Volumetric changes to montmorillonites occur during exposure to CO2. Theory-based simulations identify interactions with interlayer cations as energetically favorable for CO2 intercalation. In contrast, experimental evidence suggests CH4 does not occupy the interlayer and has only the propensity for surface adsorption. Mixed CH4:CO2 gas systems, where CH4 concentrations prevail, indicate preferential CO2 sorption as determined by in situ infrared spectroscopy and X-ray diffraction techniques. Collectively, these laboratory studies combined with a cost-based economic analysis provide a basis for identifying favorable CO2-EOR opportunities in previously fractured shale gas reservoirs approaching final stages of primary gas production. Moreover, utilization of site-specific laboratory measurements in reservoir simulators provides insight into optimum injection strategies for maximizing CH4/CO2 exchange rates to obtain peak natural gas production

Fluorocarbon adsorption in hierarchical porous frameworks

Metal-organic frameworks comprise an important class of solid-state materials and have potential for many emerging applications such as energy storage, separation, catalysis and bio-medical. Here we report the adsorption behaviour of a series of fluorocarbon derivatives on a set of microporous and hierarchical mesoporous frameworks. The microporous frameworks show a saturation uptake capacity for dichlorodifluoromethane of >4 mmol g-1 at a very low relative saturation pressure (P/Po) of 0.02. In contrast, the mesoporous framework shows an exceptionally high uptake capacity reaching >14 mmol g-1 at P/Poof 0.4. Adsorption affinity in terms of mass loading and isosteric heats of adsorption is found to generally correlate with the polarizability and boiling point of the refrigerant, with dichlorodifluoromethane > chlorodifluoromethane > chlorotrifluoromethane > tetrafluoromethane > methane. These results suggest the possibility of exploiting these sorbents for separation of azeotropic mixtures of fluorocarbons and use in eco-friendly fluorocarbon-based adsorption cooling