Super gas barrier nanocoatings are recently demonstrated by combining polyelectrolytes and clay nanoplatelets with layer-by-layer deposition. These nanobrick wall thin films match or exceed the gas barrier of SiOx and metallized films, but they are relatively stiff and lose barrier with significant stretching (≥ 10% strain). In an effort to impart stretchability, hydrogen-bonding polyglycidol (PGD) layers are added to an electrostatically bonded thin film assembly of polyethylenimine (PEI) and montmorillonite (MMT) clay. The oxygen transmission rate of a 125-nm thick PEI-MMT film increases more than 40x after being stretched 10%, while PGD-PEI-MMT trilayers of the same thickness maintain its gas barrier. This stretchable trilayer system has an OTR three times lower than the PEI-MMT bilayer system after stretching. This report marks the first stretchable high gas barrier thin film, which is potentially useful for applications that require pressurized elastomers.
Significant loss of life and property results each year from fires fueled by polyurethane found in household furnishings. Established layer-by-layer flame retardant systems were combined to produce a stacked nanocoating for flame retarding polyurethane foam. A bilayer system of chitosan (CH) and vermiculite provides a nanobrick wall exoskeleton, protecting the polyurethane long enough for an intumescing system of CH and ammonium polyphosphate to activate and form a bubbled char layer. Stacking these two recipes allows the foam to self-extinguish when exposed to a butane torch without any flame spread or shrinking of the foam, two things commonly observed with either coating alone. Cone calorimetry revealed a significant peak heat release rate reduction of 66 % relative to the uncoated foam. This study demonstrates the ability to combine flame retardant mechanisms sequentially. This nanocoating acts as an environmentally benign template for flame retarding various complex substrates, especially those found in household furnishings.
Front Cover: Boundaries are being pushed with layer‐bylayer (LbL) technology every day, and the present work has demonstrated the first stretchable gas barrier prepared with this technology. The cover image depicts an American football helmet, representing an oxygen molecule, failing to break through a transparent, stretchable film. On a molecular level, this LbL thin film (≈125‐nm thick) uses hydrogen bonding between layers to introduce a bond slipping ability that results in macro‐scale stretchiness. This stretchable barrier is important for applications requiring pressurized elastomer materials (e.g., bladders and air bags). Further details can be found in the article by K. M. Holder, B. R. Spears, M. E. Huff, M. A. Priolo, E. Harth, and J. C. Grunlan* on page 960.
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