205 research outputs found

    Structural change of fluid catalytic cracking catalysts study incorporate with coke characterization formed in heavy oil volatilization/decomposition

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    Porous structure change of catalyst and coke formation from feedstock on fluid catalytic cracking (FCC) catalyst have studied by a more comprehensive set of analyses, include 2D, 3D analyses incorporate with carbon/coke characterization teniques. Carbon/coke formed from a heavy oil volatilization/decomposition with different oil-to-FCC catalyst ratio (1:3, 1:2, 1:1, 2:1 and 3:1) to simulate the aging of FCC catalyst in a continuous oil refinery. Carbon/coke was formed for all used FCC catalyst samples that is generally increases with the increase of oil-to-FCC catalyst ratio. Coke formation has been correlated with the porosity change of the FCC catalyst, that more carbon/coke formed on the FCC catalyst due to the increment of oil-to-FCC catalyst ratio leads to the decrease of total pore volume and surface area. Zeolite is evenly distributed from the FCC catalyst particle centre to the exterior for all pristine and used FCC catalyst particles. The interior porous structure of single FCC catalyst particle is not affected by the coking. However, the exterior porous structure is completely disappear for all used FCC catalyst, that could cause by porous frame collapse and the coking clog the surface pores. The more comprehensive study of the structural change incorporate with the carbon/coke characterisation, which helps to understand the progressive degredation of FCC catalyst caused by porous structure change more in depth. Figure 1 is an example of 3 D tomogram and the radial distribution profiles of pristine FCC catalyst. Please click Additional Files below to see the full abstract

    Developments in Dilatometry for Characterisation of Electrochemical Devices

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    Since the 1970s, electrochemical dilatometry (ECD) has been used to investigate the dilation of layered host materials due to the intercalation of guest ions, atoms or molecules, and has recently gained traction in application to various electrochemical devices, such as lithium-ion batteries (LiBs), which have electrodes that undergo volume changes during cycling, resulting in particle cracking and electrode degradation. With resolution capabilities spanning tens of microns down to a few nanometres, dilatometry is a valuable tool in understanding how commonly used electrodes dilate and degrade and can therefore be of critical value in improving their performance. In recent years, there has been a plethora of studies using dilatometry as a monitoring tool for understanding operating performance in various electrochemical devices; however, to our knowledge, there has been no in-depth review of this body of research to date. This paper seeks to address this by reviewing how dilatometry works and how it has been used for the characterisation of electrochemical energy storage devices

    Comparative study of energy management systems for a hybrid fuel cell electric vehicle - A novel mutative fuzzy logic controller to prolong fuel cell lifetime

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    Hybrid fuel cell battery electric vehicles require complex energy management systems (EMS) in order to operate effectively. Poor EMS can result in a hybrid system that has low efficiency and a high rate of degradation of the fuel cell and battery pack. Many different types of EMS have been reported in the literature, such as equivalent consumption minimisation strategy and fuzzy logic controllers, which typically focus on a single objective optimisations, such as minimisation of H2 usage. Different vehicle and system specifications make the comparison of EMSs difficult and can often lead to misleading claims about system performance. This paper aims to compare different EMSs, against a range of performance metrics such as charge sustaining ability and fuel cell degradation, using a common modelling framework developed in MATLAB/Simulink - the Electric Vehicle Simulation tool-Kit (EV-SimKit). A novel fuzzy logic controller is also presented which mutates the output membership function depending on fuel cell degradation to prolong fuel cell lifetime – the Mutative Fuzzy Logic Controller (MFLC). It was found that while certain EMSs may perform well at reducing H2 consumption, this may have a significant impact on fuel cell degradation, dramatically reducing the fuel cell lifetime. How the behaviour of common EMS results in fuel cell degradation is also explored. Finally, by mutating the fuzzy logic membership functions, the MFLC was predicted to extend fuel cell lifetime by up to 32.8%

    X-ray Computed Tomography for Failure Mechanism Characterisation within Layered Pouch Cells

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    Lithium-ion battery (LIB) safety is a multi-scale problem: from the whole-cell architecture to its composite internal 3D microstructures. Substantial research is required to standardise failure assessments and optimise cell designs to reduce the risks of LIB failure. In this work, the failure response of a 1 Ah layered pouch cell with a commercially available NMC cathode and graphite anode at 100 % SOC (4.2 V) is investigated. The mechanisms of two abuse methods; mechanical (by nail penetration) and thermal (by accelerating rate calorimetry) are compared by using a suite of post-mortem analysis methods. Post-mortem whole-cell architectural changes and electrode layer deformations were analysed for both mechanisms using non-invasive X-ray computed tomography. Furthermore, changes to electrode surfaces, bulk microstructures and particle morphologies are compared by following a proposed cell disassembly and post-mortem sample preparation methodology. Building on the insights into critical architectural weak points, electrode behaviours and particle cracks, the reliability of X-ray computed tomography as a guide for LIB failure assessment is demonstrated

    On the origin and application of the Bruggeman Correlation for analysing transport phenomena in electrochemical systems

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    The widely used Bruggeman equations correlate tortuosity factors of porous media with their porosity. Finding diverse application from optics to bubble formation, it received considerable attention in fuel cell and battery research, recently. The ability to estimate tortuous mass transport resistance based on porosity alone is attractive, because direct access to the tortuosity factors is notoriously difficult. The correlation, however, has limitations, which are not widely appreciated owing to the limited accessibility of the original manuscript. We retrace Bruggemans derivation, together with its initial assumptions, and comment on validity and limitations apparent from the original work to offer some guidance on its use.<br/

    High power Nb-doped LiFePO<sub>4</sub> Li-ion battery cathodes; pilot-scale synthesis and electrochemical properties

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    AbstractHigh power, phase-pure Nb-doped LiFePO4 (LFP) nanoparticles are synthesised using a pilot-scale continuous hydrothermal flow synthesis process (production rate of 6 kg per day) in the range 0.01–2.00 at% Nb with respect to total transition metal content. EDS analysis suggests that Nb is homogeneously distributed throughout the structure. The addition of fructose as a reagent in the hydrothermal flow process, followed by a post synthesis heat-treatment, affords a continuous graphitic carbon coating on the particle surfaces. Electrochemical testing reveals that cycling performance improves with increasing dopant concentration, up to a maximum of 1.0 at% Nb, for which point a specific capacity of 110 mAh g−1 is obtained at 10 C (6 min for the charge or discharge). This is an excellent result for a high power cathode LFP based material, particularly when considering the synthesis was performed on a large pilot-scale apparatus

    Ultra high-resolution biomechanics suggest that substructures within insect mechanosensors decisively affect their sensitivity

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    Insect load sensors, called campaniform sensilla (CS), measure strain changes within the cuticle of appendages. This mechanotransduction provides the neuromuscular system with feedback for posture and locomotion. Owing to their diverse morphology and arrangement, CS can encode different strain directions. We used nano-computed tomography and finite-element analysis to investigate how different CS morphologies within one location-the femoral CS field of the leg in the fruit fly Drosophila-interact under load. By investigating the influence of CS substructures' material properties during simulated limb displacement with naturalistic forces, we could show that CS substructures (i.e. socket and collar) influence strain distribution throughout the whole CS field. Altered socket and collar elastic moduli resulted in 5% relative differences in displacement, and the artificial removal of all sockets caused differences greater than 20% in cap displacement. Apparently, CS sockets support the distribution of distal strain to more proximal CS, while collars alter CS displacement more locally. Harder sockets can increase or decrease CS displacement depending on sensor location. Furthermore, high-resolution imaging revealed that sockets are interconnected in subcuticular rows. In summary, the sensitivity of individual CS is dependent on the configuration of other CS and their substructures

    Silicon-Based Solid-State Batteries: Electrochemistry and Mechanics to Guide Design and Operation

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    Solid-state batteries (SSBs) are promising alternatives to the incumbent lithium-ion technology; however, they face a unique set of challenges that must be overcome to enable their widespread adoption. These challenges include solid-solid interfaces that are highly resistive, with slow kinetics, and a tendency to form interfacial voids causing diminished cycle life due to fracture and delamination. This modeling study probes the evolution of stresses at the solid electrolyte (SE) solid-solid interfaces, by linking the chemical and mechanical material properties to their electrochemical response, which can be used as a guide to optimize the design and manufacture of silicon (Si) based SSBs. A thin-film solid-state battery consisting of an amorphous Si negative electrode (NE) is studied, which exerts compressive stress on the SE, caused by the lithiation-induced expansion of the Si. By using a 2D chemo-mechanical model, continuum scale simulations are used to probe the effect of applied pressure and C-rate on the stress-strain response of the cell and their impacts on the overall cell capacity. A complex concentration gradient is generated within the Si electrode due to slow diffusion of Li through Si, which leads to localized strains. To reduce the interfacial stress and strain at 100% SOC, operation at moderate C-rates with low applied pressure is desirable. Alternatively, the mechanical properties of the SE could be tailored to optimize cell performance. To reduce Si stress, a SE with a moderate Young's modulus similar to that of lithium phosphorous oxynitride (∼77 GPa) with a low yield strength comparable to sulfides (∼0.67 GPa) should be selected. However, if the reduction in SE stress is of greater concern, then a compliant Young's modulus (∼29 GPa) with a moderate yield strength (1-3 GPa) should be targeted. This study emphasizes the need for SE material selection and the consideration of other cell components in order to optimize the performance of thin film solid-state batteries

    Fault diagnosis of PEMFC based on the AC voltage response and 1D convolutional neural network

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    Real-time diagnosis is required to ensure the safety, reliability, and durability of the polymer electrolyte membrane fuel cell (PEMFC) system. Two categories of methods are (1) intrusive, time consuming, or require alterations to the cell architecture but provide detailed information about the system or (2) rapid and benign but low-information-yielding. A strategy based on alternating current (AC) voltage response and one-dimensional (1D) convolutional neural network (CNN) is proposed as a methodology for detailed and rapid fuel cell diagnosis. AC voltage response signals contain within them the convoluted information that is also available via electrochemical impedance spectroscopy (EIS), such as capacitive, inductive, and diffusion processes, and direct use of time-domain signals can avoid time-frequency conversion. It also overcomes the disadvantage that EIS can only be measured under steady-state conditions. The utilization of multi-frequency excitation can make the proposed approach an ideal real-time diagnostic/characterization tool for fuel cells and other electrochemical power systems

    Enabling intercalation-type TiNb24O62 anode for sodium- and potassium-ion batteries via a synergetic strategy of oxygen vacancy and carbon incorporation

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    The key to develop earth-abundant energy storage technologies sodium- and potassium-ion batteries (SIBs and PIBs) is to identify low-cost electrode materials that allow fast and reversible Na+/K+ intercalation. Here, we report an intercalation-type material TiNb24O62 as a versatile anode for SIBs and PIBs, via a synergistic strategy of oxygen vacancy and carbon incorporation to enhance ion and electron diffusion. The TiNb24O62−x/reduced graphene oxide (rGO) composite anode delivers high reversible capacities (130 mA h g−1 for SIBs and 178 mA h g−1 for PIBs), great rate performance (54 mA h g−1 for SIBs and 37 mA h g−1 for PIBs at 1 A g−1), and superior cycle stability (73.7% after 500 cycles for SIBs and 84% after 300 cycles for PIBs). The performance is among the best results of intercalation-type metal oxide anodes for SIBs and PIBs. The better performance of TiNb24O62−x/rGO in SIBs than PIBs is due to the better reaction kinetics of the former. Moreover, mechanistic study confirms that the redox activity of Nb4+/5+ is responsible for the reversible intercalation of Na+/K+. Our results suggest that TiNb24O62−x/rGO is a promising anode for SIBs and PIBs and may stimulate further research on intercalation-type compounds as candidate anodes for large ion batteries
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