Solid State Thermoelectric Generator for Remote Applications

This paper proposes a device that utilizes thermoelectric generators (TEGs) for energy generation from solid biomass combustion, with a focus on addressing the low power electricity needs of off-grid dwellings and remote cabins in Alaska. The feasibility of a device utilizing TEG technology to convert waste heat from wood stoves into electrical power is explored, with the goal of offering a continuous and weather-independent energy source. Potential customers and stakeholders were consulted to build requirements for the system, including power output, size, ease of use, safety features, and cost considerations. The design utilizes passive water cooling to provide a temperature differential – a highly efficient strategy for thermoelectric generation. The final prototype is designed to fit the form factor of off grid cabins, occupying roughly 1ft2 on the stove and 1ft3 for the associated electronics. The device produces a steady state power of 13W with boiling water in the reservoir and a maximum of 25W intermittently. This design meets the needs of portability, affordability, and ease of use for the potential market. This system has the potential to enhance energy access and reliability in off-grid locations and offers a promising solution for improving the quality of life in remote areas

Enlisting Students to Transcribe Historical Climate and Weather Data For Research: Building Knowledge Translation Via Classroom-Based Citizen Science

DRAW (Data Rescue: Archives & Weather) is a citizen science project that asks the Canadian public to take part in transcribing millions of meteorological observations recorded between 1871 and 1963 at McGill University’s Observatory in Montreal, Quebec, which was demolished in 1963. We examine how classroom-based curricula can integrate citizen science so youth can learn more about their community via engagement with the local history of weather conditions and impacts. Conducted in March 2018, this research examined knowledge translation during a three-week course module through written reflections, classroom video footage, exit interviews, and a final group research assignment. We worked with 21 students—16- to 20-year-olds enrolled in a social science research methods course at Dawson College, a two-year collège d\u27enseignement général et professionnel (college of general and vocational education) that attracts local students and is a funded part of education in the province of Quebec. We found knowledge translation was facilitated by student engagement with their community’s history and appreciation for aiding credible scientific research. Knowledge translation suffered from attempts to include archival records that could be difficult to find, access, and read. Our work showed that citizen science, as a vehicle for community engagement and scientific literacy, requires considerable contextualization, for example, the use of frequently asked questions, tutorials, and blogs for context, and historical context to ensure knowledge translation takes place

Influence of time and ageing conditions on the properties of ferrihydrite

Natural conversion of ferrihydrite (Fh), a widespread Fe(iii)-oxyhydroxide mineral at the Earth's surface, to thermodynamically more stable iron oxides such as goethite (Gt) and hematite (Hm) is a slow process that spans months to years. Here we examined the effects of synthesis and storage conditions on the hydration, the ratio of tetrahedral to octahedral iron sites, and the transformation of naturally aged 2-line Fh at room temperature and mildly acidic pH over an ageing period of 5 years. Fh samples synthesized and aged in either aerobic or anaerobic conditions were characterized over time by XRD, SEM, thermogravimetric analysis - mass spectroscopy (TGA-MS), and X-ray absorption spectroscopies (XANES and XMCD). The findings show that the ratio of tetrahedral to octahedral Fe(iii) sites in Fh is correlated to its extent of hydration, with fresher Fh samples exhibiting a higher ratio and more bound water. Fresh Fh aged in aerobic conditions has similar bound inorganic carbon, is more hydrated, and has less tetrahedral Fe(iii) than that aged in anaerobic conditions. Hence, for relatively fresh Fh there is a link between Fh properties and storage conditions. However, the long-term ageing characteristics, such as the transformation rate and relative phase fraction of Gt and Hm products, are not noticeably impacted by storage conditions. TGA-MS measurements coupled with O K-edge XANES spectra confirm that Fh tends to lose its hydration as it ages, as expected. Corresponding Fe L2,3-edge XMCD spectra reveal that this dehydration is coupled to a steady decrease in the ratio of tetrahedral to octahedral Fe(iii) sites. In addition to the obvious constraints these findings place on making comparisons across Fh samples of different age and environmental settings, they also highlight that Fh structure, and consequently magnetism, are linked to its bound water content

Scoping studies to establish the capability and utility of a real-time bioaerosol sensor to characterise emissions from environmental sources

A novel dual excitation wavelength based bioaerosol sensor with multiple fluorescence bands called Spectral Intensity Bioaerosol Sensor (SIBS) has been assessed across five contrasting outdoor environments. The mean concentrations of total and fluorescent particles across the sites were highly variable being the highest at the agricultural farm (2.6 cm−3 and 0.48 cm−3, respectively) and the composting site (2.32 cm−3 and 0.46 cm−3, respectively) and the lowest at the dairy farm (1.03 cm−3 and 0.24 cm−3, respectively) and the sewage treatment works (1.03 cm−3 and 0.25 cm−3, respectively). In contrast, the number-weighted fluorescent fraction was lowest at the agricultural site (0.18) in comparison to the other sites indicating high variability in nature and magnitude of emissions from environmental sources. The fluorescence emissions data demonstrated that the spectra at different sites were multimodal with intensity differences largely at wavelengths located in secondary emission peaks for λex 280 and λex 370. This finding suggests differences in the molecular composition of emissions at these sites which can help to identify distinct fluorescence signature of different environmental sources. Overall this study demonstrated that SIBS provides additional spectral information compared to existing instruments and capability to resolve spectrally integrated signals from relevant biological fluorophores could improve selectivity and thus enhance discrimination and classification strategies for real-time characterisation of bioaerosols from environmental sources. However, detailed lab-based measurements in conjunction with real-world studies and improved numerical methods are required to optimise and validate these highly resolved spectral signatures with respect to the diverse atmospherically relevant biological fluorophores

Why do sulfone-containing polymer photocatalysts work so well for sacrificial hydrogen evolution from water?

Many of the highest-performing polymer photocatalysts for sacrificial hydrogen evolution from water have contained dibenzo[b,d]thiophene sulfone units in their polymer backbones. However, the reasons behind the dominance of this building block are not well understood. We study films, dispersions, and solutions of a new set of solution-processable materials, where the sulfone content is systematically controlled, to understand how the sulfone unit affects the three key processes involved in photocatalytic hydrogen generation in this system: light absorption; transfer of the photogenerated hole to the hole scavenger triethylamine (TEA); and transfer of the photogenerated electron to the palladium metal co-catalyst that remains in the polymer from synthesis. Transient absorption spectroscopy and electrochemical measurements, combined with molecular dynamics and density functional theory simulations, show that the sulfone unit has two primary effects. On the picosecond timescale, it dictates the thermodynamics of hole transfer out of the polymer. The sulfone unit attracts water molecules such that the average permittivity experienced by the solvated polymer is increased. We show that TEA oxidation is only thermodynamically favorable above a certain permittivity threshold. On the microsecond timescale, we present experimental evidence that the sulfone unit acts as the electron transfer site out of the polymer, with the kinetics of electron extraction to palladium dictated by the ratio of photogenerated electrons to the number of sulfone units. For the highest-performing, sulfone-rich material, hydrogen evolution seems to be limited by the photogeneration rate of electrons rather than their extraction from the polymer

Natural law, non-voluntary euthanasia, and public policy

© 2019 by Emerald Publishing Limited. Natural Law philosophy asserts that there are universally binding and universally evident principles that can be determined to guide the actions of persons. Moreover, many of these principles have been enshrined in both statute and common law, thus ensuring their saliency for staff and institutions charged with palliative care. The authors examine the often emotive and politicized matter of (non-voluntary) euthanasia – acts or omissions made with the intent of causing or hastening death – with reference to Natural Law philosophy. This leads us to propose a number of important public policy remedies to ensure dignity in dying for the patient, and their associates

Effect of pathology type and severity on the distribution of MRI signal intensities within the degenerated nucleus pulposus: application to idiopathic scoliosis and spondylolisthesis

<p>Abstract</p> <p>Background</p> <p>Disc degeneration is characterized by a loss of cellularity, degradation of the extracellular matrix, and, as a result, morphological changes and biomechanical alterations. We hypothesized that the distribution of the MR signal intensity within the nucleus zone of the intervertebral disc was modified according to the pathology and the severity of the pathology. The objective of this study was to propose new parameters characterizing the distribution of the signal intensity within the nucleus zone of lumbar intervertebral discs, and to quantify these changes in patients suffering from spondylolisthesis or idiopathic scoliosis.</p> <p>Methods</p> <p>A retrospective study had been performed on T2-weighted MR images of twenty nine patients suffering from spondylolisthesis and/or scoliosis. The high intensity zone of the nucleus pulposus was semi-automatically detected. The distance "DX" between the center weighted by the signal intensity and the geometrical center was quantified. The sum of the signal intensity on the axis perpendicular to the longitudinal axis of the disc was plotted for each position of the longitudinal axis allowing defining the maximum sum "SM" and its position "PSM".</p> <p>Results</p> <p>"SM" was clearly higher and "PSM" was more shifted for scoliosis than for spondylolisthesis. A two-way analysis of variance showed that the differences observed on "DX" were not attributed to the pathology nor its severity, the differences observed on "SM" were attributed to the pathology but not to its severity, and the differences observed on "PSM" were attributed to both the pathology and its severity.</p> <p>Conclusions</p> <p>The technique proposed in this study showed significant differences in the distribution of the MR signal intensity within the nucleus zone of intervertebral discs due to the pathology and its severity. The dependence of the "PSM" parameter to the severity of the pathology suggests this parameter as a predictive factor of the pathology progression. This new technique should be useful for the early diagnosis of intervertebral disc pathologies as it highlights abnormal patterns in the MRI signal for low severity of the pathology.</p

A Rescorla-Wagner Drift-Diffusion Model of Conditioning and Timing

Computational models of classical conditioning have made significant contributions to the theoretic understanding of associative learning, yet they still struggle when the temporal aspects of conditioning are taken into account. Interval timing models have contributed a rich variety of time representations and provided accurate predictions for the timing of responses, but they usually have little to say about associative learning. In this article we present a unified model of conditioning and timing that is based on the influential Rescorla-Wagner conditioning model and the more recently developed Timing Drift-Diffusion model. We test the model by simulating 10 experimental phenomena and show that it can provide an adequate account for 8, and a partial account for the other 2. We argue that the model can account for more phenomena in the chosen set than these other similar in scope models: CSC-TD, MS-TD, Learning to Time and Modular Theory. A comparison and analysis of the mechanisms in these models is provided, with a focus on the types of time representation and associative learning rule used

The effect of glycol side chains on the assembly and microstructure of conjugated polymers

Conjugated polymers with glycol-based chains, are emerging as a material class with promising applications as organic mixed ionic-electronic conductors, particularly in bioelectronics and thermoelectrics. However, little is still known about their microstructure and the role of the side chains in determining intermolecular interactions and polymer packing. Here, we use the combination of electrospray deposition and scanning tunneling microscopy to determine the microstructure of prototypical glycolated conjugated polymers (pgBTTT and p(g2T-TT)) with submonomer resolution. Molecular dynamics simulations of the same surface-adsorbed polymers exhibit an excellent agreement with the experimental images, allowing us to extend the characterization of the polymers to the atomic scale. Our results prove that, similarly to their alkylated counterparts, glycolated polymers assemble through interdigitation of their side chains, although significant differences are found in their conformation and interaction patterns. A model is proposed that identifies the driving force for the polymer assembly in the tendency of the side chains to adopt the conformation of their free analogues, i.e., polyethylene and polyethylene glycol, for alkyl or ethylene glycol side chains, respectively. For both classes of polymers, it is also demonstrated that the backbone conformation is determined to a higher degree by the interaction between the side chains rather than by the backbone torsional potential energy. The generalization of these findings from two-dimensional (2D) monolayers to three-dimensional thin films is discussed, together with the opportunity to use this type of 2D study to gain so far inaccessible, subnm-scale information on the microstructure of conjugated polymers

Understanding structure-activity relationships in linear polymer photocatalysts for hydrogen evolution

Conjugated polymers have sparked much interest as photocatalysts for hydrogen production. However, beyond basic considerations such as spectral absorption, the factors that dictate their photocatalytic activity are poorly understood. Here we investigate a series of linear conjugated polymers with external quantum efficiencies for hydrogen production between 0.4 and 11.6%. We monitor the generation of the photoactive species from femtoseconds to seconds after light absorption using transient spectroscopy and correlate their yield with the measured photocatalytic activity. Experiments coupled with modeling suggest that the localization of water around the polymer chain due to the incorporation of sulfone groups into an otherwise hydrophobic backbone is crucial for charge generation. Calculations of solution redox potentials and charge transfer free energies demonstrate that electron transfer from the sacrificial donor becomes thermodynamically favored as a result of the more polar local environment, leading to the production of long-lived electrons in these amphiphilic polymers