Publications by authors named "Harishchandra Jirimali"

Carbon materials are versatile in nature due to their unique and modifiable surface and ease of production. Nanostructured carbon materials are gaining importance due to their high surface area for application in the energy, biotechnology, biomedical, and environmental fields. According to their structures, carbon allotropes are classified as carbon nanodots, carbon nanoparticles, graphene, oxide, carbon nanotubes, and fullerenes.

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This review describes the preparation of nonedible vegetable oil (NEVO)-based polyols and their application in anticorrosive and antimicrobial polyurethane (PU) coatings. PUs are a class of versatile polymers made up of polyols and isocyanates. Renewable vegetable oils are promising resources for the development of ecofriendly polyols and the corresponding PUs.

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A new family of chitosan-cross-linked osmium polymer composites was prepared and its electrochemical properties were examined. The composites were prepared by quaternization of the poly(4-vinylpyridine) osmium bipyridyl polymer (PVP-Os) which was then cross-linked with chitosan, yielding PVP-Os/chitosan. Films made of the composites showed improved mass and electron transport owing to the porous and hydrophilic structure which is derived from the cross-links between the Os polymer and chitosan.

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A redox active polymer, hydroquinone modified chitosan (Q-chitosan) was synthesized and characterized by IR and (1)H NMR spectroscopy. The nanocomposite of Q-chitosan with carbon was prepared and used to construct a stable conductive film on the electrode surface. The SEM studies confirms that the Q-chitosan/C composite covers the electrode surface with polymer embedded 50 nm size carbon particles.

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Less is more: Nickel cyclam complexes are known as efficient catalysts for the electrochemical reduction of CO(2) to CO, despite having overvoltages of more than 0.6 V. Incorporating [Ni(cyclam)](2+) into poly(allylamine) through axial coordination of pyridine enables the electrochemical reduction of CO(2) to CO near the thermodynamic potential of -0.

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