Polymer nanocomposites exhibit unique physicochemical properties that cannot be obtained with individual components acting alone. Polymer nanocomposites have attracted significant research interests due to their promising potential for versatile applications ranging from environmental remediation, energy storage, electromagnetic (EM) absorption, sensing and actuation, transportation and safety, defense systems, information industry, to novel catalysts, etc. In particular, polymer nanocomposites have attracted intensive research interest for solving both energy and environmental issues. This review paper mainly focuses on the most recent advances in polymer nanocomposites for energy storage (i.e., electrochemical capacitors and batteries), energy saving (i.e., electrochromic devices and carbon dioxide capture), and anticorrosion (conductive and non-conductive polymer nanocomposite anticorrosive coatings) applications.

Dicalcium phosphate was prepared by ethylenediaminetetraacetic acid as a calcium chelating agent, and further explored to remove the fluoride ions from aqueous solution. The as-prepared samples main existed in the monetite phase from the result of XRD. The dried sample consisted of small nanoparticles and displayed irregular particles with a size of ca. 3 μm due to the agglomeration. The fluoride removal ability was evaluated by batch adsorption experiments. The as-prepared adsorbent exhibited the enhanced fluoride removal behaviour with the maximum adsorption capacity of 66.72 mg/g from the Langmuir isotherm model, which was higher than that of other previously reported calcium phosphate. The adsorbent could be utilized in the wide pH range of 3–10. The adsorption kinetics could be better described by the pseudo-second-order model than first-second-order model. The co-existing anions had a negligible influence on the fluoride adsorption. The investigation of adsorption mechanism suggested that the chemical reaction and/or dissolution – precipitation mechanism should be dominant in the fluoride adsorption process, accompanying with electronic interaction and ions exchange, which enhanced the fluoride removal performance.

Recycled newspaper (NP) shows excellent potential as a reinforcement for polymer composites. Herein, high-strength laminated composites were prepared by using NP laminas as reinforcement and high-density polyethylene (HDPE) films as matrix. Physical and mechanical properties of the laminated composites were measured. It was found that the flexural strength of the composites had a good linear relationship to its density, with R² = 0.9853. The flexural and tensile strength of the composites at the maximum density (1.40 g/cm³) reached up to 95.6 ± 2.4 MPa and 99.4 ± 0.8 MPa, respectively. SEM results showed that NP layer inside the composite became compact at the hot pressing time of 40 min, because the melted HDPE permeated into the NP layers to bond the NP fibers. Quantitative description of the composite porosity was conducted according to the density of the composite. The 24-h water absorption of the composite was highly related to its porosity, with R² = 0.8994. This study reveals that density of laminated composites is an important parameter, which could be used to forecast the mechanical strength, and its derived value, porosity of the composites, could be used to predict the water absorption behavior of the composite.

A high strength recycled newspaper (NP)/high density polyethylene (HDPE) laminated composite was developed using NP laminas as reinforcement and HDPE film as matrix. Herein, NP fiber was modified with stearic acid (SA) to enhance the water resistance of the NP laminas and NP/HDPE composite. The effects of heat treatment and SA concentration on the water resistance and tensile property of NP and composite samples were investigated. The chemical structure of the NP was characterized with X-ray diffractometer, X-ray photoelectron spectroscopy and attenuated total reflectance Fourier transform infrared spectra techniques. The surface and microstructure of the NP sheets were observed by scanning electron microscopy. An expected high-water resistance of NP sheets was achieved due to a chemical bonding that low surface energy SA were grafted onto the modified NP fibers. Results showed that the hydrophobicity of NP increased with increasing the stearic acid concentration. The water resistance of the composite laminates was depended on the hydrophobicity of the NP sheets. The lowest value of 2 h water absorption rate (3.3% ± 0.3%) and thickness swelling rate (2.2% ± 0.4%) of composite were obtained when the SA concentration was 0.15 M. In addition, the introduction of SA can not only enhance the water resistance of the composite laminates, but also reduce the loss of tensile strength in wet conditions, which shows potential in outdoor applications.

Waste newspaper are currently used in a single way and have low utilization rates. In this paper, the optimal process of preparing environmentally friendly layered composites by using waste newspaper combined with polypropylene film lamination was studied. The effects of hot-pressing temperature, hot-pressing time and paper content on the properties of the composites were analyzed. The results showed that under the process conditions of hot-pressing temperature 180 °C, compression time 20 min and paper content 66.7%, the obtained composite material had a flexural strength of 126 MPa, a tensile strength of 95 MPa, an impact strength of 5.3 kJ/m² and a water absorption thickness expansion ratio of 3.2%. Tensile performance increased by 164% compared to the original waste newspaper. Compared to our previous work, the hot processing time had been cut in half and costs were lower. In terms of creep properties, the unrecoverable strain rate was reduced by 57.5% compared to pure polypropylene. The results show that the material can maintain excellent flexural strength, tensile strength and water absorption performance while making good use of waste newspaper.