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Polymer nanocomposites are a class of composite materials containing polymer continuous phase as matrix and inorganic nanoparticles as fillers. Combining the advantages of both polymer and nanofillers, polymer nanocomposites can yield some desirable functionalities that cannot be achieved by the individual components, thus exhibiting tremendous potential for a variety of applications. However, their performances markedly depend on the dispersion and distribution of nanofillers in the polymer matrix. Recently, in situ emulsion polymerization has been demonstrated to be a powerful approach for the preparation of multifunctional polymer nanocomposites with good dispersion and homogeneous distribution of nanofillers. In this review, the fundamentals of polymer nanocomposites and their preparation strategies are briefly discussed, and then are comprehensively summarized recent advances in the design, preparation, functionalization, and applications of polymer nanocomposites via in situ emulsion polymerization. The particular focus is placed on the strategies for achieving homogeneous and good dispersion of nanofillers within polymer matrixes. Moreover, the current challenges and future opportunities of in situ emulsion polymerization to polymer nanocomposites are discussed to motivate future contributions and explore new possibilities. [ABSTRACT FROM AUTHOR]

The high speed development of industries such as new energy power, medical instruments, under¬ground exploration, and high power pulses are demanding more and more dielectric capacitors. Polymer based film capacitors are attracting attention for their high power density, high breakdown field strength, high reliability, low loss, and small size. However, the low energy density due to the low dielectric constant of the polymer itself has limited IS application n high-end fields. And polymer as an effective way to enhance the energy density by compounding with other organic or inorganic materials in different ways. This paper introduces the current research status of polymer based film capacitors compounded with inorganic materials, analyzes the advantages and shortcomings of different compounding methods, and discusses the future development prospects of polymer based film capacitors. [ABSTRACT FROM AUTHOR]

Compared with commercial lithium batteries with liquid electrolytes, all‐solid‐state lithium batteries (ASSLBs) possess the advantages of higher safety, better electrochemical stability, higher energy density, and longer cycle life; therefore, ASSLBs have been identified as promising candidates for next‐generation safe and stable high‐energy‐storage devices. The design and fabrication of solid‐state electrolytes (SSEs) are vital for the future commercialization of ASSLBs. Among various SSEs, solid polymer composite electrolytes (SPCEs) consisting of inorganic nanofillers and polymer matrix have shown great application prospects in the practice of ASSLBs. The incorporation of inorganic nanofillers into the polymer matrix has been considered as a crucial method to achieve high ionic conductivity for SPCE. In this review, the mechanisms of Li+ transport variation caused by incorporating inorganic nanofillers into the polymer matrix are discussed in detail. On the basis of the recent progress, the respective contributions of polymer chains, passive ceramic nanofillers, and active ceramic nanofillers in affecting the Li+ transport process of SPCE are reviewed systematically. The inherent relationship between the morphological characteristics of inorganic nanofillers and the ionic conductivity of the resultant SPCE is discussed. Finally, the challenges and future perspectives for developing high‐performance SPCE are put forward. This review aims to provide possible strategies for the further improvement of ionic conductivity in inorganic nanoscale filler‐reinforced SPCE and highlight their inspiration for future research directions. [ABSTRACT FROM AUTHOR]

Due to the rapid expansion of nanotechnology and the increasing range of nanomaterials under production and development, a significant amount of research interest has been dedicated to the innovative exploitations of various inorganic nanomaterials in environmental applications. The incorporation of inorganic nanomaterials as fillers within a polymeric matrix has expanded opportunities to produce a multifunctional nanocomposite membrane that is capable of performing tasks beyond separation alone. The architectures and performances of these nanocomposite membranes have triumphed over polymeric membranes to overcome the underlying conspicuous drawbacks. This review aims to shed more light on the roles of inorganic nanomaterials in advancing the characteristics and separation performance of polymeric ultrafiltration membranes. Inorganic nanofillers such as metal oxides, metals and carbon-based materials are incorporated into polymeric membranes to render the desired properties for ultrafiltration separations. Novel strategies using a wide range of these inorganic nanomaterials have been well explored and established for the manufacturing of membrane with significantly enhanced properties that are highly desired to heighten the separation performances. With the renaissance of this emerging innovative technology, many possible solutions and valuable options can be offered to serve as the primary driver in excelling ultrafiltration membrane technology. [ABSTRACT FROM PUBLISHER]

Hydrogels have been widely used in water purification. However, there is not much discussion and comparison about the effects of different nanofillers on the reinforcement and adsorption performances of hydrogels, which can be subjected to rapid water flow and possess strong adsorption ability. In this work, polyacrylamide (PAAM)-sodium alginate (SA) interpenetrating polymer network-structured hydrogels were prepared by in situ polymerization. PAAM formed the first flexible network and SA constructed the second rigid network. Three kinds of inorganic nanoparticles including carbon nanotubes (CNTs), nanoclays (NCs), and nanosilicas (NSs) were incorporated into a PAAM-SA matrix via hydrogen bond. The obtained hydrogels exhibited a macroporous structure with low density (≈1.4 g/cm3) and high water content (≈83%). Compared with neat PAAM-SA, the hydrogels with inorganic nanoparticles possessed excellent mechanical strengths and elasticities, and the compression strength of PAAM-SA-NS reached up to 1.3 MPa at ε = 60% by adding only 0.036 g NS in a 30 g polymer matrix. However, CNT was the best filler to improve the adsorption capacity owing to its multi-walled hollow nanostructure, and the adsorption capacity of PAAM-SA-CNT was 1.28 times higher than that of PAAM-SA. The prepared hydrogels can be potential candidates for use as absorbents to treat wastewater. [ABSTRACT FROM AUTHOR]