Professor of Chemical, Biological, and Materials Engineering at @USouthFlorida. Research in #Polymers #SoftMaterials #Thermodynamics. Views are my own.

Joined February 2015
David S. Simmons retweeted
The formula for reinforced rubber is so effective that we've counted on it for nearly 100 years. But scientists had never reached a verdict as to why it works so well. gizmodo.com/after-100-years-…
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(the answer is no) read here: doi.org/10.1021/acs.macromol… feel free to DM if you cannot access! – at Philadelphia, PA
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Very excited about this new paper from our group (former student @_Drayerv2 ), on the origins of the molecular weight dependence of Tg. We think these findings will ultimate require the textbook understanding of this trend to be rewritten. lnkd.in/eAnpc2rj 🧵
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At least one model, a substantial Tg dependence on molecular weight is observed even when the ends are dynamically identical to the interior. Even in models where a chain end effect is observed, its importance weakens on cooling such that it has little effect on Tg.
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These findings are inconsistent with chain end dilution models of the molecular weight Tg dependence. They suggest a need to reopen the problem of the Tg molecular weight dependence, with attention given to more modern theories of Tg and its dependence on molecular weight.
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David S. Simmons retweeted
The Boston Globe printed my letter today:
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David S. Simmons retweeted
Our new paper in @Nature with @sanatkk and @TomislavRovis, and Eugene Chen reports a new method that compatibilizes immiscible mixed plastics. So happy to contribute to this collaboration and excited about the future potential. nature.com/articles/s41586-0…
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Pre-print out! So proud of the culmination of my PhD work in this paper.
At #APSMarch, I gave a talk based on work by my former student @pierrekawak on simulations of low-T phase diagrams relevant for polymer crystallization. We now have a pre-print up: doi.org/10.26434/chemrxiv-20… We'd love any feedback or questions.
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Our new paper in @NaturePhysics, with K. Schweizer and A. Phan, reveals a signature of a combined caging and elasticity origin of the #glasstransition within dynamics at the surface of glass-forming liquids. Surface gradients have long-range tails! rdcu.be/c8jTu 🧵
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This finding provides compelling new support for the physics underlying the ECNLE model of glass formation. In essence, this long-range 1/z gradient is a direct signature of collective elastic physics within the ECNLE theory.
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The shorter-range gradient is of mixed nature, combining elastic effects with a gradient in segmental localization length scale. Our results thus point to a dual-barrier mechanism of glass-formation, with contributions from local caging and from long-ranged collective elasticity.
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