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Nicholas A. Brunelli

Researcher at Ohio State University

Publications -  51
Citations -  2920

Nicholas A. Brunelli is an academic researcher from Ohio State University. The author has contributed to research in topics: Catalysis & Aldol condensation. The author has an hindex of 21, co-authored 47 publications receiving 2449 citations. Previous affiliations of Nicholas A. Brunelli include Emory University & Georgia Institute of Technology.

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Interfacial microfluidic processing of metal-organic framework hollow fiber membranes

TL;DR: A potentially scalable route for making high-quality gas separation membranes in a high-surface-area configuration using a two-solvent interfacial approach for positional control over membrane formation and an in situ module for membrane fabrication and permeation is presented.
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Zeolitic imidazolate frameworks: next-generation materials for energy-efficient gas separations.

TL;DR: A review is given of the state-of-the-art in ZIF synthesis procedures and novel ZIF formation pathways as well as their application in energy efficient separations.
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Dramatic enhancement of CO2 uptake by poly(ethyleneimine) using zirconosilicate supports.

TL;DR: It is suggested that the important role of the surface properties of the oxide support in these polymer/oxide composite adsorbents has been largely overlooked and that the properties may be even further enhanced in the future by tuning the acid/base properties ofthe support.
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Hybrid Zeolitic Imidazolate Frameworks: Controlling Framework Porosity and Functionality by Mixed-Linker Synthesis

TL;DR: In this paper, the synthesis and characterization of hybrid ZIFs with mixed linkers in the framework are described, producing materials with properties distinctly different from the parent frameworks (ZIF-8, ZIF-90, and ZIF 7).
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Tuning Cooperativity by Controlling the Linker Length of Silica-Supported Amines in Catalysis and CO2 Capture

TL;DR: Short linkers limit the beneficial amine-silanol cooperativity in aldol condensations, resulting in lower catalytic rates than with the C3+ linkers, and the adsorptive cooperativity exhibits similar trends for CO(2) capture efficiency.