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Bassil M. El-Zaatari

Researcher at Northwestern University

Publications -  11
Citations -  262

Bassil M. El-Zaatari is an academic researcher from Northwestern University. The author has contributed to research in topics: Azide & Cycloaddition. The author has an hindex of 5, co-authored 10 publications receiving 97 citations. Previous affiliations of Bassil M. El-Zaatari include University of Delaware.

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Molecular Characterization of Polymer Networks.

TL;DR: A critical overview of the current characterization techniques available to understand the relation between the molecular properties and the resulting performance and behavior of polymer networks, in the absence of added fillers, can be found in this paper.
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Cross-linker control of vitrimer flow

TL;DR: It is shown that cross-linker reactivity represents an additional design parameter to tune stress relaxation rates in vitrimers and can mix different cross- linkers in a single material in order to further modulate the stress relaxation behavior.
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Mechanical and Structural Consequences of Associative Dynamic Cross-Linking in Acrylic Diblock Copolymers

TL;DR: In this paper, the composition of low-Tg n-butylacrylate-block-(acetoxyaceto)ethyl acrylate block polymers is investigated as a strategy to tune the properties of dynamically cross-linked vinylogous urethane vitrimers.
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Blue-light activated rapid polymerization for defect-free bulk Cu(I)-catalyzed azide–alkyne cycloaddition (CuAAC) crosslinked networks

TL;DR: A visible-light (470 nm wavelength) sensitive Type II photoinitiator system is developed for bulk Cu(i)-catalyzed azide-alkyne cycloaddition reactions in crosslinked networks allowing the formation of defect-free glassy networks which exhibit a narrow glass transition temperature.
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Towards understanding the kinetic behaviour and limitations in photo-induced copper(i) catalyzed azide-alkyne cycloaddition (CuAAC) reactions.

TL;DR: The kinetic behaviour of the photo-induced copper(i) catalyzed azide-alkyne cycloaddition (CuAAC) reaction was studied in detail using real-time Fourier transform infrared (FTIR) spectroscopy on both a solvent-based monofunctional and a neat polymer network forming system, showing near first-order kinetics on copper and photoinitiator concentrations up to a threshold value in which the kinetics switch to zeroth-order.