The versatility of polymeric materials as healing agents to prevent any structure failure and their ability to restore their initial mechanical properties has attracted interest from many researchers. Various applications of the self-healing polymeric materials are explored in this paper. The mechanism of self-healing, which includes the extrinsic and intrinsic approaches for each of the applications, is examined. The extrinsic mechanism involves the introduction of external healing agents such as microcapsules and vascular networks into the system. Meanwhile, the intrinsic mechanism refers to the inherent reversibility of the molecular interaction of the polymer matrix, which is triggered by the external stimuli. Both self-healing mechanisms have shown a significant impact on the cracked properties of the damaged sites. This paper also presents the different types of self-healing polymeric materials applied in various applications, which include electronics, coating, aerospace, medicals, and construction fields. It is expected that this review gives a significantly broader idea of self-healing polymeric materials and their healing mechanisms in various types of applications.

Polymers are being used in many applications all around the world. However, there are some drawbacks in the properties of polymers that could hamper their usage in certain applications. Therefore, a new material polymer composite was introduced. A polymer composite is a polymer-based material with the addition of a filler. Many researchers have reported the improvement in the properties of a polymer when a filler was introduced. This helps minimize the disadvantages of using a polymer. As a result, polymer composite products can be used in many industries, such as automobile, aerospace, biomedical, and packaging. Fillers derived from natural minerals, such as dolomite, are among the best reinforcement materials for polymeric materials because they are plentiful and low cost, have high rigidity and hardness, and even have tailorable surface chemistry. The use of dolomite as a filler in a polymer composite system has gained increasing attention in recent years after researchers successfully proved that it is capable of improving the mechanical, physical, and thermal properties of various polymeric materials. However, chemical or physical treatment/modification of raw dolomite is needed in order to prepare it as an efficient reinforcing filler. This procedure helps to improve the performance of the resultant polymer composites. This article reviews the usage of dolomite as a filler in a variety of polymeric materials and how it improved the performance of the polymer composite materials. It also highlights several methods that have been used for the purpose dolomite’s treatment/modification. Furthermore, the role of dolomite as a co-filler or a hybrid filler in a polymer composite system is also discussed, revealing the great potential and prospect of this mineral filler in the field of polymer composites for advanced applications.

The in vitro biostability and biocompatibility of ethyl vinyl acetate (EVA) nanocomposites incorporating organically modified montmorillonite (organo-MMT) were investigated as new candidate material for biomedical applications. The in vitro treatment of neat EVA and EVA nanocomposites was performed by immersing the materials in oxidizing and hydrolytic agents, at a temperature of 37 °C, for 4 weeks. The in vitro mechanical properties of the materials under these environmentally challenging conditions were assessed. Based on morphology studies, the degree of MMT dispersion and exfoliation decreased as the nanofiller loading increased. The EVA containing 1 wt% organo-MMT exhibited the best nanofiller dispersion and exfoliation characteristics. The surface degradation features of this nanocomposite were seen to be smoother than those of neat EVA and other EVA nanocomposites. Furthermore, the EVA nanocomposites have improved mechanical properties in comparison with the neat EVA, and these properties were less affected by the in vitro conditions. The best in vitro mechanical properties were achieved when 1 wt% of organo-MMT was added into the EVA. It was postulated that the presence of a better dispersed and exfoliated organo-MMT layered structure introduced a more tortuous path for the diffusion of oxidants and water molecules, thereby decreasing their permeation towards the EVA molecular chains. Therefore, the degradation kinetics within the EVA molecular chains were at a lower rate, which resulted in enhanced biostability. Furthermore, the toughness of the hydrated EVA (exposed to PBS at 37 °C) was greatly enhanced with the addition of the 1 wt% organo-MMT. The biocompatibility assessment suggests that the EVA nanocomposites are not cytotoxic, and thus have fulfilled the prerequisite to be further developed as a biomedical material.