Polyurethanes Modified by Ionic Liquids and Their Applications.

Polyurethane (PU) refers to the polymer containing carbamate groups in its molecular structure, generally obtained by the reaction of isocyanate and alcohol. Because of its flexible formulation, diverse product forms, and excellent performance, it has been widely used in mechanical engineering, electronic equipment, biomedical applications, etc. Through physical or chemical methods, ionic groups are introduced into PU, which gives PU electrical conductivity, flame-retardant, and antistatic properties, thus expanding the application fields of PU, especially in flexible devices such as sensors, actuators, and functional membranes for batteries and gas absorption. In this review, we firstly introduced the characteristics of PU in chemical and microphase structures and their related physical and chemical performance. To improve the performance of PU, ionic liquids (ILs) were applied in the processing or synthesis of PU, resulting in a new type of PU called ionic PU. In the following part of this review, we mainly summarized the fabrication methods of IL-modified PUs via physical blending and the chemical copolymerization method. Then, we summarized the research progress of the applications for IL-modified PUs in different fields, including sensors, actuators, transistors, antistatic films, etc. Finally, we discussed the future development trends and challenges faced by IL-modified PUs.

Crystallization-driven surface segregation and surface structures in poly(L-lactide)-block-poly(ethylene glycol) copolymer thick films.

In this work, we used poly(L-lactide)-block-poly(ethylene glycol) (PLLA-b-PEG) copolymer thick films to investigate the effect of crystallization on surface segregation, surface crystal orientation, and morphology by attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR), reflection optical microscopy (ROM), and two-dimensional grazing incident wide-angle X-ray scattering (2D GIWAXS) methods. ATR-FTIR results indicated that the surface fraction of PLLA block increased from 0.48 to 0.79 when T(c,PLLA) increased from 70 to 110 °C. Polarized ATR-FTIR and 2D GIWAXS results indicated that PLLA crystal lamellae preferentially oriented parallel to the film surface with increasing T(c,PLLA). The surface crystallinity of PLLA was almost independent of T(c,PLLA), while the surface crystallinity of PEG decreased with increasing T(c,PLLA). On the basis of surface crystal orientation and crystallization kinetics, we suggested that the excess of PLLA component at the surface was mainly dominated by a coupling effect of crystallization behavior and surface segregation.

Liquid crystalline assembly of coil-rod-coil molecules with lateral methyl groups into 3-D hexagonal and tetragonal assemblies.

In this paper, we report the synthesis and self-assembly behavior of coil-rod-coil molecules, consisting of three biphenyls linked through a vinylene unit as a conjugated rod segment and poly(ethylene oxide) (PEO) with a degree of polymerization (DP) of 7, 12 and 17, incorporating lateral methyl groups between the rod and coil segments as the coil segment. Self-organized investigation of these molecules by means of differential scanning calorimetry (DSC), thermal polarized optical microscopy (POM) and X-ray diffraction (XRD) reveals that the lateral methyl groups attached to the surface of rod and coil segments, dramatically influence the self-assembling behavior in the liquid-crystalline mesophase. Molecule 1 with a relatively short PEO coil length (DP=7) self-assembles into rectangular and oblique 2-dimensional columnar assemblies, whereas molecules 2 and 3 with DP of 12 and 17 respectively, spontaneously self-organize into unusual 3-dimensional hexagonal close-packed or body-centered tetragonal assemblies.

Chitosan-based double cross-linked ionic hydrogels as a strain and pressure sensor with broad strain-range and high sensitivity.

A conductive hydrogel P(AAm-co-AA)/CS-Fe3+ with double cross-linked networks was fabricated using a one-step polymerization by UV irradiation and a soaking process in Fe(NO3)3 solution. In this hydrogel, the rigid chain of chitosan (CS) and the soft chain of copolymer P(AAm-co-AA) with acrylic acid (AA) and acrylamide (AAm) act as the backbone, among which large amounts of hydrogen bonds are formed by the amino, hydroxyl, and carboxyl groups on the two polymers. Ferric irons (Fe3+) are introduced and form coordination interactions with carboxyl and amino groups of the polymers. The double cross-linked interactions in the system can enhance the tensile strength and toughness of the hydrogel. Thus, the prepared P(AAm-co-AA)/CS-Fe3+ hybrid network hydrogel shows excellent mechanical properties in many aspects: a strength of up to 550 kPa, a broad strain-range up to 800%, fast self-recovery ability (30 min), and low hysteresis strain (<100%). The conductive hydrogel demonstrates high strain sensitivity (gauge factor (GF) = 6.6 at a strain of 700%) as a flexible sensor. Human movements (for example, finger bending, vocal cord vibration, and other human activities) can be sensitively detected using the P(AAm-co-AA)/CS-Fe3+ hydrogel sensor.

Concentric ring pattern formation in a competing crystallization and phase separation process.

Spherulitic patterns usually form in the single process of crystallization in polymer blends. But when phase separation intervenes under deep quench, the radial growth of the initial spherulitic patterns tends to invert into concentric alternating crystalline-/amorphous-rich ring structures. Within crystalline-rich regions, lateral lamellae orient in the tangential direction rather than in the usual radial direction. We demonstrate the determining factor for this first observed phenomenon is the concentration deviation enhanced phase separation dynamics at the growth interface of crystals.

Designing function-oriented artificial nanomaterials and membranes via electrospinning and electrospraying techniques.

The sister technologies, electrospinning and electrospraying provide a facile and universal synthesis method for the continuous preparation of nanostructured materials. Through adjusting the synthesis parameters, rich electrospun and electrosprayed nanomaterials, scaffolds, membranes with tunable composition (inorganic, polymeric, hybrid, etc.), shape (sphere, films, scaffold, etc.), morphology and inner structure (solid, hollow, core-shell, co-axial, etc.) can be selectively elaborated. This review provides an overview of the design of functional nanostructured materials, porous scaffolds and membranes by electrospinning and electrospraying techniques. Key experimental parameters and synthesis strategy are emphasized to reveal the synthesis-component-structure-property relationship and eventually realize the targeted functions through predictable synthesis. Potential applications in tissue engineering, medicine, membrane filtration and lithium battery are highlighted.

High performance graphene oxide based rubber composites.

In this paper, graphene oxide/styrene-butadiene rubber (GO/SBR) composites with complete exfoliation of GO sheets were prepared by aqueous-phase mixing of GO colloid with SBR latex and a small loading of butadiene-styrene-vinyl-pyridine rubber (VPR) latex, followed by their co-coagulation. During co-coagulation, VPR not only plays a key role in the prevention of aggregation of GO sheets but also acts as an interface-bridge between GO and SBR. The results demonstrated that the mechanical properties of the GO/SBR composite with 2.0 vol.% GO is comparable with those of the SBR composite reinforced with 13.1 vol.% of carbon black (CB), with a low mass density and a good gas barrier ability to boot. The present work also showed that GO-silica/SBR composite exhibited outstanding wear resistance and low-rolling resistance which make GO-silica/SBR very competitive for the green tire application, opening up enormous opportunities to prepare high performance rubber composites for future engineering applications.