Robust self-healing thermoplastic elastomers are expected to have repeated healing capability, remarkable mechanical properties, transparency, and superior toughness. The phase-locked design in this work provides excellent tensile mechanical properties and efficient healability at a moderate temperature due to the dynamic disulfide bonds embedded in the hard segments and mainly being locked in the viscoelastic hard microphase region. The self-healing elastomers exhibit a maximum tensile stress of 25 MPa and a fracture strain of over 1600%, which are quite prominent compared to previous reports. The nanoscale domains of the elastomer are smaller than the wavelength of visible light by microphase separation control resulting in colorless, nearly 100% transparency, and are as good as quartz glasses. The high dynamics of the phase-locked disulfide bonds renders a high healing efficiency of scratches on the surface within 60 s at 70 °C. The rapid scratch healing and complete transparency recovery of the elastomers provide new avenues in the highly transparent surface or protective films which finds potential applications for precision optical lenses, flexible display screens, and automobile or aircraft lighting finishes.

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The structure, morphology and thermal properties of biobased and biodegradable poly(butylene succinate-ran-butylene azelate) random copolyesters with a wide composition range were studied. These PBS-ran-PBAz copolymers can crystallize in the entire composition range despite being random, displaying a eutectic point when their melting point is plotted as a function of composition. Wide Angle Xray Scattering (WAXS) studies confirmed isodimorphic behavior where PBS-rich copolymers crystallize with PBS type unit cells with some PBAz repeating units inclusions and vice versa for PBAz-rich copolymers. Away from eutectic compositions the copolymers exhibit only one crystalline phase (PBS-rich or PBAzrich crystalline phases) while at the eutectic point both phases can crystallize. The only double crystalline copolymer amongst those prepared had a composition close to the eutectic point of 45 mol% PBS (and 55 mol% PBAz). The crystallization of the two phases occurred in the same temperature range upon cooling from the melt at 10ºC/min in a DSC (i.e., coincident crystallization). Self-nucleation (SN) studies of the PBS-rich phase were performed. After SN, the separate crystallization of each phase was clearly observed during cooling from the self-nucleation temperature (i.e., PBS and PBAz-rich phases). Small Angle X-ray Scattering (SAXS) experiments were performed for the first time for this type of isodimorphic copolymers. The results show that the lamellar long period is a strong function of composition. While limited inclusions of PBAz units within the crystal lattice only cause a slight expansion of the PBS component unit cell, the increase of comonomer content produces an unexpected synergistic increase in long periods and lamellar thickness values. In the case of the only double crystalline copolymer examined, the PBS-rich phase forms space filling spherulites (observed by Polarized Light Optical Microscopy, PLOM) at higher temperatures that template the superstructural morphology of the copolymer. These PBS-rich phase spherulites contain radial lamellar stacks whose long period was determined by SAXS. Upon further cooling, the PBAz-rich phase crystallizes in the intra-spherulitic amorphous regions with newly form lamellae that have their own distinct long period according to SAXS results. AFM observations of the PBS-rich crystalline lamellae confirmed the lamellar thickness and long spacings determined by SAXS. A schematic morphological model of the mixed spherulites produced by this double crystalline diblock copolymer is proposed based on the experimental evidences collected by SAXS, PLOM and AFM.

Poly(lactic acid) (PLA) is one of the most promising alternatives for petrochemical-based plastics. Crystallization mediation provides the simplest and most practical approach for enhancing the properties of PLA. Here, recent advances in understanding the relationship between crystalline structure and properties of PLA are summarized. Methods for manipulating crystallization towards high-performance PLA materials are introduced.

The classic deformation mechanism of the Gaussian model of Haward and Thackray was utilized to treat the true stress−strain behaviors of a family of novel polyether-b-amide segmented copolymers based on the crystalline hard segments of polyamide1012 and the amorphous soft segments of poly­(tetramethylene oxide). The results showed that the deformation behaviors of the plastic copolymers abided by the Gaussian model, causing the modulus G of the strain-induced hardening process to depend on the weight percentage of the polyamide segments in the copolymers. By contrast, the deformation of elastomeric copolymers deviated from the model because of the occurrence of strain-induced crystallization in the soft polyether sections at large strains, which negated the Gaussian assumption; i.e., the random coil conformation was maintained even under substantial stretching. The onset point of deviation was, for the first time, quantitatively identified by in situ FTIR and further confirmed by in situ WAXD/SAXS.

The fast mixing of aqueous solutions of calcium chloride and sodium carbonate could immediately result in amorphous calcium carbonate (ACC). Under vigorous stirring, the formed ACC in the precipitation system will dissolve first and, then, transform within minutes to produce crystalline forms of vaterite and calcite. After that, the solution-mediated mechanism dominates the transformation of the thermodynamically unstable vaterite into the thermodynamically stable calcite. Although ACC is the least stable form of the six anhydrous phases of calcium carbonate (CaCO(3)), it could be, however, produced and stabilized by a variety of organisms. To better understand the formation-transformation mechanism of ACC and vaterite into calcite, ex-situ methods (i.e., scanning electron microscopy, Fourier transform infrared spectroscopy, and X-ray diffraction spectroscopy) were used to characterize the formation-transformation process of ACC and vaterite in aqueous systems without organic additives, showing that ACC sampled at different conditions has different properties (i.e., lifetime, morphology, and spectrum characterization). It is also very interesting to capture the obviously polycrystalline particles of CaCO(3) during the transformation process from vaterite to calcite, which suggests the formation mechanism for the calcite superstructure with multidimensional morphology.

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