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Victoria B. Oyelami

Bio: Victoria B. Oyelami is an academic researcher from Ladoke Akintola University of Technology. The author has an hindex of 1, co-authored 1 publications receiving 13 citations.

Papers
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TL;DR: In this article, the authors present some advancements in the usages of metal-organic frameworks (MOFs) for the adsorptive removal of different contaminants from the ecosystems, including heavy metals, CO2, chlorinated volatile organic compounds (CVOCs), dyes, pesticides, food additives, veterinary, pharmaceutical and personal care products (PPCP), antibiotics, biological and chemical weapons, other industrial chemicals, etc.

63 citations


Cited by
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TL;DR: In this paper, a comparison of various AOPs in terms of nitro-products formation mechanisms and the associated environmental issues is presented, where the sonochemical nitrogen fixation is a key mechanism for the formation of Nitro-compounds in ultrasound-based AOP.

139 citations

Journal ArticleDOI
TL;DR: In this paper , a comparison of various AOPs in terms of nitro-products formation mechanisms and the associated environmental issues is presented, where the sonochemical nitrogen fixation is a key mechanism for the formation of Nitro-compounds in ultrasound-based AOP.

139 citations

01 Sep 2017
TL;DR: In this paper, the de-solvation process and the transport of Li+ in the preformed solid electrolyte interphase (SEI) on electrodes until the Li+ accepts an electron at the electrode and becomes a Li in the electrode.
Abstract: Understanding the factors limiting Li+ charge transfer kinetics in Li-ion batteries is essential in improving the rate performance, especially at lower temperatures. The Li+ charge transfer process involved in the lithium intercalation of graphite anode includes the step of de-solvation of the solvated Li+ in the liquid electrolyte and the step of transport of Li+ in the preformed solid electrolyte interphase (SEI) on electrodes until the Li+ accepts an electron at the electrode and becomes a Li in the electrode. Whether the de-solvation process or the Li+ transport through the SEI is a limiting step depends on the nature of the interphases at the electrode and electrolyte interfaces. Several examples involving the electrode materials such as graphite, lithium titanate (LTO), lithium iron phosphate (LFP), lithium nickel cobalt aluminum oxide (NCA) and solid Li+ conductor such as lithium lanthanum titanate or Li-Al-Ti-phosphate are reviewed and discussed to clarify the conditions at which either the de-solvation or the transport of Li+ in SEI is dominating and how the electrolyte components affect the activation energy of Li+ charge transfer kinetics. How the electrolyte additives impact the Li+ charge transfer kinetics at both the anode and the cathode has been examined at the same time in 3-electrode full cells. The resulting impact on Li+ charge transfer resistance, Rct, and activation energy, Ea, at both electrodes are reported and discussed.

66 citations

Journal ArticleDOI
TL;DR: In this paper , a review of recent results addressing the adsorption of PFAS on activated carbons and metal-organic frameworks (MOF) is presented, which emphasizes the effects of these modifications on the PFAS mechanism and brings the critical assessment of the advantages and disadvantages of both groups as PFAS adsorbents.

48 citations

Journal ArticleDOI
TL;DR: In this paper, a review focusing on the adsorption of PFAS on activated carbons and metal-organic frameworks (MOF) is presented, emphasizing the effects of these modifications on the adaption mechanism and in the critical assessment of the advantages and disadvantages of both groups as the PFAS adsorbents.

48 citations