Supramolecular polymers are widely utilized and applied in self-assembly or self-healing materials, which can be repaired when damaged. Normally, the healing process is classified into two types, including extrinsic and intrinsic self-healable materials. Therefore, the aim of this work is to review the intrinsic self-healing strategy based on supramolecular interaction or non-covalent interaction and molecular recognition to obtain the improvement of mechanical properties. In this review, we introduce the main background of non-covalent interaction, which consists of the metal–ligand coordination, hydrogen bonding, π–π interaction, electrostatic interaction, dipole–dipole interaction, and host–guest interactions, respectively. From the perspective of mechanical properties, these interactions act as transient crosslinking points to both prevent and repair the broken polymer chains. For material utilization in terms of self-healing products, this knowledge can be applied and developed to increase the lifetime of the products, causing rapid healing and reducing accidents and maintenance costs. Therefore, the self-healing materials using supramolecular polymers or non-covalent interaction provides a novel strategy to enhance the mechanical properties of materials causing the extended cycling lifetime of products before replacement with a new one.

Shape memory elastomers have revolutionised the world since their introduction in the 20th century. The ability to tailor chemical structures to produce a family of materials in wide-ranging forms with versatile properties has propelled them to be ubiquitous. Recent challenges in the end-of-life management of polymeric materials should prompt us to ask, ‘what innovations in polymeric materials can make a strong case for their use as efficient materials?’ The development of smart elastomers that can acquire, convey, or process a stimulus (such as temperature, pressure, electromagnetic field, moisture, and chemical signals) and reply by creating a useful effect, specifically a reversible change in shape, is one such innovation. Here, we present a brief overview of shape memory elastomers (SMEs) and thereafter a review of recent advances in their development. We discuss the complex processing of structure-property relations and how they differ for a range of stimuli-responsive SMEs, self-healing SMEs, thermoplastic SMEs, and antibacterial and antifouling SMEs. Following innovations in SEMs, the SMEs are forecast to have significant potential in biotechnology based on their tailorable physical properties that are suited to a range of different external stimuli.

This study developed a natural rubber (NR) composite reinforced with surface-modified pineapple leaf fibres (PALFs) and hemp fibres (HFs) using a layer-by-layer (sandwich-like) fabrication method. The objectives were to increase the utilisation of the natural fibres as reinforcing agents and to investigate the impact of silane fibre surface modification on the properties of the sandwich composites. Fibre surface characterisation was performed using Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and X-ray diffraction (XRD) to confirm the presence of functional groups from silane and cellulose. The wettability and adhesion properties of the modified fibres were also evaluated. The mechanical properties were investigated via single-fibre tensile tests. Composites with 50 phr silane-treated PALF showed the best compromise in terms of interface adhesion (48.3 mJ/m²) and tensile strength (6 MPa). This result was also supported by scanning electron microscopy (SEM), which revealed the absence of voids between the fibres and the NR matrix. Furthermore, dynamic mechanical analysis showed that the PALF composite treated with silane at 50 phr exhibited the best viscoelastic behaviour. NR composites with 50 phr silane-treated PALF have mechanical properties suitable for potential applications in engineering products.