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1.
  • Hank, Andrew M., et al. (author)
  • Comparative Characterisation of CNS/Epoxy and BN/Epoxy Nanodielectrics using Electrical Tree PD Measurements and Atomic Force Microscopy
  • 2020
  • In: International Journal of Engineering Research in Africa. - 1663-3571 .- 1663-4144. ; 48, s. 24-37
  • Journal article (peer-reviewed)abstract
    • This paper contributes to the body of knowledge on the efforts to develop nanodielectrics as the next generation of insulation material. The time-to-failure under electrical tree-induced degradation of 1.09-1.35 vol.% hexagonal BN/Epoxy was found to be 3 times longer than in clean epoxy. For 0.31-0.33 vol.% CNS/Epoxy the time-to-failure was 24 times longer than the clean epoxy. The electrical treeing partial discharge behaviour in the BN/Epoxy and CNS/Epoxy showed distinct time-evolution characteristics different from those in the clean epoxy. The improved electrical tree endurance in BN/Epoxy relative to the clean epoxy can be attributed to increased mechanical stiffness. The superiority of the CNS/Epoxy as a nanodielectric is notable. The effect is suggested to be due to the electron affinity properties of the carbon nanospheres at appropriate dispersion levels.
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2.
  • Momodu, Damilola, et al. (author)
  • Stable ionic-liquid-based symmetric supercapacitors from Capsicum seed-porous carbons
  • 2019
  • In: Journal of Electroanalytical Chemistry. - : Elsevier BV. - 1572-6657. ; 838, s. 119-128
  • Journal article (peer-reviewed)abstract
    • In this study, a symmetric ionic-liquid based supercapacitor was assembled with porous carbon derived from Capsicum (bell pepper) seeds. The “peppered”-activated carbon (ppAC) was synthesized using varying amounts of KHCO 3 activating agent (AA) at 850 °C carbonization temperature. The best device performance reported was recorded with optimum amounts of AA to raw material. The need for less amount of AA is crucial if the entire activation/carbonization process is to be scaled-up with the cost and final product yield also being important for a viable synthesis. A mechanism of saturation of pores with unreacted AA which leads to lower porosity metrics in the samples with increasing the amount of AA during carbonization/activation was also proposed. Using an ionic liquid electrolyte, 1-ethyl-3-methylimidazolium bistrifluorosulfonylimide (EMIM-TFSI), the ppAC-based supercapacitor operated up to a maximum cell voltage of 3.20 V. A specific energy of 37 Wh kg −1 was obtainable with a corresponding practical power density of 0.6 kW kg −1 at 0.5 A g −1 . A specific energy of ∼26 Wh kg −1 was still achievable when the applied current was doubled to 1.0 A g −1 and a high cyclic stability (approx. 99% coulombic efficiency) was proven over 25,000 cycles. Further ageing test performed on the device revealed a remarkable improvement in the electrochemical performance after a 180 h (ca. 1 week) floating time. The obtained results also confirmed a uniquely distributed porous carbon in which the complete utilization of the entire less-corrosive KHCO 3 AA for optimal pore activation at elevated carbonization temperatures. Thus, the efficient design combinations for stable, high-energy and power ionic liquid-based supercapacitors with cheaper biomass-based materials are demonstrated.
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