112 research outputs found

    Flexible aromatic disulfide monomers for high-performance self-healable linear and cross-linked poly(urethane-urea) coatings

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    Implementation of the self-healing concept in coatings is challenging because they have to combine mechanical strength and chain mobility. This challenge is addressed in this work by studying the effect of the polymer microstructure on the mechanical properties and self-healing ability of waterborne poly(urethane-urea) coatings containing aromatic disulfide dynamic bonds. The structural modifications studied are the concentration and flexibility of the aromatic disulfide units and the effect of cross-linking. The effects and limits of these structural changes on the mechanical properties of the polymers and their healability were determined via a combination of DMA measurements, tensile tests, and rheological and scratch closure experiments. It was found that the flexibility of the disulfide unit was key to develop more efficient self-healing materials which offer the necessary molecular mobility for self-healing while simultaneously maintaining a level of mechanical strength that are essential for coating applications.The European Union’s Horizon 2020 research and innovation programme is accredited for the financial support through Project TRACKWAY-ITN 642514 under the Marie Sklodowska-Curie grant agreement. N.B. acknowledges the financial support obtained through the Post-Doctoral fellowship Juan de la Cierva - Incorporación (IJCI-2016-28442), from the Ministry of Economy and Competitiveness of Spai

    Synthesis of mechanically strong waterborne poly(urethane-urea)s capable of self-healing at elevated temperatures

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    Although various chemistries have been introduced into polyurethanes in order to obtain self-healing abilities, implementing these materials in applications requiring high strength is challenging as strong materials imply a limited molecular motion, but without movement of polymer chains self-healing is not possible. Here, waterborne poly(urethane-urea)s (PU(U)s) based on aromatic disulfide compounds are developed which balance these contradictory requirements by presenting good mechanical properties at room temperature, while showing the mobility necessary for healing when moderately heated. The influence of hard monomers on the stability and mobility of the materials is investigated by scratch closure, cut healing and rheological measurements, so that the limits of the readily available aromatic disulfide compounds, bis(4-aminophenyl)- and bis(4-hydroxyphenyl)disulfide, can be determined. Subsequently, a modified aromatic disulfide compound, bis[4-(3'-hydroxypropoxy)phenyl]disulfide, with increased reactivity, solubility and flexibility is synthesized and incorporated into the PU backbone, so that materials with more attractive mechanical properties, reaching ultimate tensile strengths up to 23 MPa, and self-healing abilities at elevated temperatures could be obtained.The European Union’s Horizon 2020 research and innovation programme is accredited for the financial support through Project TRACKWAY-ITN 642514 under the Marie Sklodowska-Curie grant agreement. N.B. acknowledges the financial support obtained through the Post-Doctoral fellowship Juan de la Cierva - Incorporación (IJCI-2016-28442), from the Ministry of Economy and Competitiveness of Spai

    Phase Separation Driven On-Demand Debondable Waterborne Pressure-Sensitive Adhesives

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    A waterborne pressure-sensitive adhesive (PSA) that shows high adhesive performance and easy debondability on demand without leaving residues on the substrate (adhesive failure) has been developed. A key component of the PSA is a semicrystalline phase that is beneficial for the adhesive properties and that becomes fluid when heated above the melting temperature. Migration of this liquid-like polymer to the substrate-adhesive interface and hardening upon cooling results in a hard non-tacky interface that facilitates debonding. The effect of the particle morphology on the debonding ability is discussed.This research was funded by AkzoNobe
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