Numerical analysis of thermal cycling during a multi-stage energy pile thermal response test

Energy piles are emerging as convenient alternative to the more traditional borehole heat exchangers (BHEs) to provide heating/cooling to buildings, as they remove the need for special purpose excavations and can accommodate more pipes, thus enhancing energy performance. However, their different aspect ratio compared to BHEs requires different modelling tools and dedicated thermal response testing, to achieve adequate thermal design. In this work, the results of an extended multi-stage thermal response test (TRT) carried out on a single energy pile installed in London Clay are presented in terms of both fluid temperature data and concrete temperature, measured by vibrating wire strain gauges and optic fibre sensors. The results are then explored in detail by means of a finite element numerical code, able to account for both convective heat exchange in the fluid, between the fluid and the solids and transient heat diffusion in the concrete and the ground. Analysis of the TRT field data shows that during the later stages of the test there is clear evidence of cyclic changes in performance. Investigation of these effects using the numerical model raises the possibility that there could be some alteration of the properties of the soil-pile contact during the test. Hypotheses for the observed behaviour are tentatively put forward and discussed with work recommended to further investigate the percieved phenomena

Unraveling the role of protein dynamics in dihydrofolate reductase catalysis

Protein dynamics have controversially been proposed to be at the heart of enzyme catalysis, but identification and analysis of dynamical effects in enzyme-catalyzed reactions have proved very challenging. Here, we tackle this question by comparing an enzyme with its heavy (15N, 13C, 2H substituted) counterpart, providing a subtle probe of dynamics. The crucial hydride transfer step of the reaction (the chemical step) occurs more slowly in the heavy enzyme. A combination of experimental results, quantum mechanics/molecular mechanics simulations, and theoretical analyses identify the origins of the observed differences in reactivity. The generally slightly slower reaction in the heavy enzyme reflects differences in environmental coupling to the hydride transfer step. Importantly, the barrier and contribution of quantum tunneling are not affected, indicating no significant role for “promoting motions” in driving tunneling or modulating the barrier. The chemical step is slower in the heavy enzyme because protein motions coupled to the reaction coordinate are slower. The fact that the heavy enzyme is only slightly less active than its light counterpart shows that protein dynamics have a small, but measurable, effect on the chemical reaction rate

Transient x-ray diffraction used to diagnose shock compressed Si crystals on the Nova laser

Transient x-ray diffraction is used to record time-resolved information about the shock compression of materials. This technique has been applied on Nova shock experiments driven using a hohlraum x-ray drive. Data were recorded from the shock release at the free surface of a Si crystal, as well as from Si at an embedded ablator/Si interface. Modeling has been done to simulate the diffraction data incorporating the strained crystal rocking curves and Bragg diffraction efficiencies. Examples of the data and post-processed simulations are presented

Comparison of two different models for pile thermal response test interpretation

Thermal response tests (TRTs) are regularly used to characterise the thermal resistance of borehole heat exchangers and to assess the thermal conductivity of the surrounding ground. It is becoming common to apply the same in situ testing technique to pile heat exchangers, despite international guidance suggesting that TRTs should be limited to hole diameters of 152 mm (6 in.). This size restriction arises from the increased thermal inertia of larger diameter heat exchangers, which invalidates the assumption of a steady state within the concrete needed to interpret the test data by traditional line source analysis techniques. However, new methods of analysis for pile heat exchangers have recently been developed that take account of the transient behaviour of the pile concrete. This paper applies these new methods to data from a multi-stage TRT conducted on a small diameter test pile. The thermal conductivity and thermal resistance determined using this method are then compared with those from traditional analytical approaches based on a line source analysis. Differences between the approaches are discussed, along with the observation that the thermal resistance may not be constant over the different test stages

Investigation of cycling-induced microstructural degradation in silicon-based electrodes in lithium-ion batteries using X-ray nanotomography

The microstructural degradation of a composite silicon electrode at different stages in its cycle life was investigated in 3D using X-ray nano-computed tomography. A reconstructed volume of 36 μm × 27 μm × 26 μm from the composite electrode was imaged in its pristine state and after 1, 10 and 100 cycles. Particle fracturing and phase transformation was observed within the electrode with increased cycling. In addition, a distinct, lower X-ray attenuating phase was clearly resolved, which can be associated with surface film formation resulting from electrolyte breakdown and with silicon particle phase transformation. Changes in quantified microstructural properties such as phase volume fraction and particle specific surface area were tracked. Electrode performance loss is associated with loss of active silicon. These imaging results further highlight the capability of high resolution X-ray tomography to investigate the role of electrode microstructure in battery degradation and failure

Porous metal–organic frameworks for enhanced performance silicon anodes in lithium-ion batteries

Maintaining the physical integrity of electrode microstructures in Li-ion batteries is critical to significantly extend their cycle life. This is especially important for high-capacity anode materials such as silicon, whose operational volume expansion exerts huge internal stress within the anode, resulting in electrode destruction and capacity fade. In this study, we demonstrate that by incorporating metal–organic frameworks (MOFs) with carboxylate organic linkers into Si-based anodes, a stable and flexible pore network is generated to maximize and maintain Li-ion flux throughout the electrode’s architecture. We show that the zirconium carboxylate MOF UiO-67 is a versatile comaterial to boost performance and mitigate the rate of anode degradation that presently limits the lifetime of Si anodes. The cage-like pores in UiO-67 and flexural properties of the 4,4′-biphenyldicarboxylate organic linker are proposed to create robust “ionophores” in the anode film to enhance longer term durability and performance

High-efficiency, high-speed, and low-noise photonic quantum memory

We present a demonstration of simultaneous high-efficiency, high-speed, and low-noise operation of a photonic quantum memory. By leveraging controllable collisional dephasing in a neutral barium atomic vapor, we demonstrate a significant improvement in memory efficiency and bandwidth over existing techniques. We achieve greater than 95% storage efficiency and 26% total efficiency of 880 GHz bandwidth photons, with $\mathcal{O}(10^{-5})$ noise photons per retrieved pulse. These ultrabroad bandwidths enable rapid quantum information processing and contribute to the development of practical quantum memories with potential applications in quantum communication, computation, and networking

In situ measurements of near-surface hydraulic conductivity in engineered clay slopes

In situ measurements of near-saturated hydraulic conductivity in fine grained soils have been made at six exemplar UK transport earthwork sites: three embankment and three cutting slopes. This paper reports 143 individual measurements and considers the factors that influence the spatial and temporal variability obtained. The test methods employed produce near-saturated conditions and flow under constant head. Full saturation is probably not achieved due to preferential and by-pass flow occurring in these desiccated soils. For an embankment, hydraulic conductivity was found to vary by five orders of magnitude in the slope near-surface (0 to 0.3 metres depth), decreasing by four orders of magnitude between 0.3 and 1.2 metres depth. This extremely high variability is in part due to seasonal temporal changes controlled by soil moisture content, which can account for up to 1.5 orders of magnitude of this variability. Measurements of hydraulic conductivity at a cutting also indicated a four orders of magnitude range of hydraulic conductivity for the near-surface, with strong depth dependency of a two orders of magnitude decrease from 0.2 to 0.6 metres depth. The main factor controlling the large range is found to be spatial variability in the soil macro structure generated by wetting/drying cycle driven desiccation and roots. The measurements of hydraulic conductivity reported in this paper were undertaken to inform and provide a benchmark for the hydraulic parameters used in numerical models of groundwater flow. This is an influential parameter in simulations incorporating the combined weather/vegetation/infiltration/soil interaction mechanisms that are required to assess the performance and deterioration of earthwork slopes in a changing climate

Thermal Adaptation of Dihydrofolate Reductase from the Moderate ThermophileGeobacillus stearothermophilus

The thermal melting temperature of dihydrofolate reductase from Geobacillus stearothermophilus (BsDHFR) is 30 °C higher than that of its homologue from the psychrophile Moritella profunda. Additional proline residues in the loop regions of BsDHFR have been proposed to enhance the thermostability of BsDHFR, but site-directed mutagenesis studies reveal that these proline residues contribute only minimally. Instead, the high thermal stability of BsDHFR is partly due to removal of water-accessible thermolabile residues such as glutamine and methionine, which are prone to hydrolysis or oxidation at high temperatures. The extra thermostability of BsDHFR can be obtained by ligand binding, or in the presence of salts or cosolvents such as glycerol and sucrose. The sum of all these incremental factors allows BsDHFR to function efficiently in the natural habitat of G. stearothermophilus, which is characterized by temperatures that can reach 75 °C

Synthesis of layered silicon-graphene hetero-structures by wet jet milling for high capacity anodes in Li-ion batteries

While silicon-based negative electrode materials have been extensively studied, to develop high capacity lithium-ion batteries (LIBs), implementing a large-scale production method that can be easily transferred to industry, has been a crucial challenge. Here, a scalable wet-jet milling method was developed to prepare a silicon-graphene hybrid material to be used as negative electrode in LIBs. This synthesized composite, when used as an anode in lithium cells, demonstrated high Li ion storage capacity, long cycling stability and high-rate capability. In particular, the electrode exhibited a reversible discharge capacity exceeding 1763 mAh g−1 after 450 cycles with a capacity retention of 98% and a coulombic efficiency of 99.85% (with a current density of 358 mA g−1). This significantly supersedes the performance of a Si-dominant electrode structures. The capacity fade rate after 450 cycles was only 0.005% per cycle in the 0.05–1 V range. This superior electrochemical performance is ascribed to the highly layered, silicon-graphene porous structure, as investigated via focused ion beam in conjunction with scanning electron microscopy tomography. The hybrid electrode could retain 89% of its porosity (under a current density of 358 mA g−1) after 200 cycles compared with only 35% in a Si-dominant electrode. Moreover, this morphology can not only accommodate the large volume strains from active silicon particles, but also maintains robust electrical connectivity. This confers faster transportation of electrons and ions with significant permeation of electrolyte within the electrode. Physicochemical characterisations were performed to further correlate the electrochemical performance with the microstructural dynamics. The excellent performance of the hybrid material along with the scalability of the synthesizing process is a step forward to realize high capacity/energy density LIBs for multiple device applications