Publications by authors named "U J Etim"

Supported metal catalysts are essential to a plethora of processes in the chemical industry. The overall performance of these catalysts depends strongly on the interaction of adsorbates at the atomic level, which can be manipulated and controlled by the different constituents of the active material (, support and active metal). The description of catalyst activity and the relationship between active constituent and the support, or metal-support interactions (MSI), in heterogeneous (thermo)catalysts is a complex phenomenon with multivariate (dependent and independent) contributions that are difficult to disentangle, both experimentally and theoretically.

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CuZnO/AlO is the industrial catalyst used for methanol synthesis from syngas (CO + H) and is also promising for the hydrogenation of CO to methanol. In this work, we synthesized AlO nanorods (n-AlO) and impregnated them with the CuZnO component. The catalysts were evaluated for the hydrogenation of CO to methanol in a fixed-bed reactor.

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Utilizing CO as a sustainable carbon source to form valuable products requires activating it by active sites on catalyst surfaces. These active sites are usually in or below the nanometer scale. Some metals and metal oxides can catalyze the CO transformation reactions.

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Light-weight metallic aero-sponges are highly desirable for electronics, energy storage, catalysis and environmental remediation. Although several fabrication methods have been developed, the mechanical strength and the structural fatigue resistance of the metallic aero-sponges remain unsatisfactory. Loofah sponge is known for its mechanical strength and grease absorption due to its highly ordered hierarchical laminae-trestle-laminae (L-T-L) microstructure.

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Gold nanoparticles (Au NPs) as an active noble-metal site have received great attention because of its superior catalytic activity in diverse reactions. However, the activity of Au NPs is strongly dependent on its size and dispersion degree. Therefore, we developed an efficient solid-state reduction (SSR) strategy for the first time to promote the dispersion degree and size of Au NPs in template-occluded KIT-6 (AK) as a support by taking advantage of (i) 3-dimentonal cubic mesoporous structure of support (ii) confined spaces present between template (Pluronic (P) 123) and silica wall of AK where Au NPs locate (iii) interaction of both P123 as template and silica walls of AK with Au NPs highly efficient for Au NPs dispersion and (iv) SSR strategy which avoids competitive adsorption of solvent in the conventional fabrication process.

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