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    A New Route to Highly Stretchable and Soft Inorganic–Organic Hybrid Elastomers Using Polydimethylsiloxane as Crosslinker of Epoxidized Natural Rubber
    (New York, NY [u.a.] : Wiley InterScience, 2021) Banerjee, Shib Shankar; Banerjee, Susanta; Wießner, Sven; Janke, Andreas; Heinrich, Gert; Das, Amit
    Sulfur or peroxide crosslinking is the most common and conventional method to develop elastomeric materials. A new approach to crosslink epoxidized natural rubber (ENR) by aminopropyl terminated polydimethylsiloxane (AT-PDMS) is described, intending to develop a new kind of hybrid organic–inorganic elastomers. The curing reaction is accelerated by using hydroquinone as a catalyst. The formation of the hybrid structure is evident from the appearance of two glass transition temperatures, at −1 and −120 °C, for the ENR and PDMS phases, respectively. The curing reaction is found to be of first order with respect to amine concentration with the estimated activation energy of ≈62 kJ mol−1. Comparing the mechanical properties to a typical ENR-sulfur system leads to the conclusion that the ENR/AT-PDMS hybrid structure is highly stretchable and soft, as demonstrated by its relatively higher strain at failure (up to ≈630%), and lower hardness and modulus values. The higher stretchability and soft nature of the material are achieved by introducing flexible PDMS chains during the curing process resulting to a hybrid elastomer networks. This kind of soft but robust materials can find several applications in diverse fields, such as soft robotics, flexible, and stretchable electronics.
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    Tailor-Made Functional Polymethacrylates with Dual Characteristics of Self-Healing and Shape-Memory Based on Dynamic Covalent Chemistry
    (New York, NY [u.a.] : Wiley InterScience, 2020) Mondal, Prantik; Behera, Prasanta K.; Voit, Brigitte; Böhme, Frank; Singha, Nikhil K.
    New shape memory polymers with self-healing behavior are obtained by thermoreversible Diels–Alder (DA) cross-linking of a furfuryl group-containing star-block copolymer with 1,1'-(methylenedi-4,1-phenylene)bismaleimide. The star-block copolymer consisting of a 3-arm polycaprolactone (PCL) core and a polyfurfuryl methacrylate shell is synthesized by reversible addition–fragmentation chain transfer (RAFT) polymerization. For this, a 3-arm macro-RAFT agent based on PCL is converted with an appropriate amount of furfuryl methacrylate in the presence of a radical initiator. Films of the DA network are partly insoluble at ambient temperatures. After annealing at 120 °C the films become completely soluble because of the progressing retro-DA reaction. Evaporation of the solvent and subsequent annealing at 60 °C restores the original insoluble state of the material. By means of a scratch test and tensile tests on cut and subsequently mended samples it is shown that the retro-DA reaction facilitates self-healing. Additionally, the films show pronounced shape memory effects with reasonable shape recovery and fixity ratios, which are attributed to the melting and crystallization of the PCL phase. © 2020 The Authors. Published by WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
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    A Theoretical and Experimental Analysis of the Effect of Nanoclay on Gas Perm-Selectivity of Biodegradable PLA/EVA Blends in the Presence and Absence of Compatibilizer
    (New York, NY [u.a.] : Wiley InterScience, 2020) Karimpour-Motlagh, Navid; Moghadam, Abolfazl Salehi; Khonakdar, Hossein Ali; Jafari, Seyed Hassan; Wagenknecht, Udo; Kasbi, Sina Farahani; Shojaei, Shahrokh; Mirzaee, Ramin
    Poly (lactic acid) (PLA)-based compounds are widely used in thin-film and food packaging industries. Herein, PLA/ethylene vinyl acetate copolymer (EVA)/nanoclay nanocomposites are prepared in various compositions by melt blending. The gas permeability against N2, CO2, and O2 gases is determined as a function of composition and morphology of the nanocomposites. Inclusion of high aspect ratio of platelet-like nanoclay to the blend reduces the gas diffusion. The best barrier properties against all gases is observed on introducing 5 wt% poly(ethylene/n-butyl acrylate glycidyl methacrylate) copolymer as compatibilizer to the PLA/EVA/nanoclay (75/25/5) system. The scanning and transmission electron microscopic analyses and wide-angle X-ray scattering studies reveal that inclusion of compatibilizer to the filled-blends improves the blend morphology, dispersion state, and intercalation level of clay platelets which are preferably localized at the interface of the blend. Analysis of selectivity parameter (a) shows the lowest O2 permeability and the highest aCO2/N2 and aO2/N2 values for the compatibilized filled-blend (75/25/5/5). In situ aspect ratio of clay and the degree of intercalation are theoretically evaluated based on the permeability data using various empirical models. It is found that the compatibilized filled-blend has the highest aspect ratio and intercalation level that are responsible for the optimum perm-selectivity performance. © 2020 The Authors. Published by Wiley-VCH GmbH
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    Short-Term Morphology Relaxation of Thermoplastic Polyurethane Elastomers after Fast Strain Steps
    (New York, NY [u.a.] : Wiley InterScience, 2020) Stribeck, Almut; Schneider, Konrad; Eling, Berend; Pöselt, Elmar
    Strain steps are applied to elastomers in a pneumatic relaxometer and monitored by small-angle X-ray scattering (SAXS). The relaxometer provides a rise time of 13 ms for strain pulses of step height ?e = ±1 in strain. The basic character of the 2D SAXS frames is examined and corresponding invariants Q(t) are analyzed. Three thermoplastic polyurethanes (TPU) of hardness 85 Shore A with different soft segments are studied both unannealed and annealed. The first response of all materials is a fast morphology conversion which finishes within tmc =250 ms. Because it has been untraceable, it is characterized by a settling stroke Q(tmc) - Q(0). The second response is a slow morphology adjustment process which complies with logarithmic relaxation. It is characterized by a relaxation rate DQ = Q(10 t)/Q(t) - 1. Comparison indicates that the nanoscopic morphology relaxation processes appear to have little direct relation to the macroscopic stress relaxation curves. The materials differ with respect to hard-domain morphology stability and morphology recovery. Most unstable is the morphology of the annealed polyether-based material. It forms nanofibrillary entities when strained. © 2020 The Authors. Published by Wiley-VCH GmbH