Academic research regarding polymeric materials has been of great interest. Likewise, polymer industries are considered as the most familiar petrochemical industries. Despite the valuable and continuous advancements in various polymeric material technologies over the last century, many varieties and advances related to the field of polymer science and engineering still promise a great potential for exciting new applications. Research, development, and industrial support have been the key factors behind the great progress in the field of polymer applications. This work provides insight into the recent energy applications of polymers, including energy storage and production. The study of polymeric materials in the field of enhanced oil recovery and water treatment technologies will be presented and evaluated. In addition, in this review, we wish to emphasize the great importance of various functional polymers as effective adsorbents of organic pollutants from industrial wastewater. Furthermore, recent advances in biomedical applications are reviewed and discussed.

Thermal energy storage (TES) technologies are considered as enabling and supporting technologies for more sustainable and reliable energy generation methods such as solar thermal and concentrated solar power. A thorough investigation of the TES system using paraffin wax (PW) as a phase changing material (PCM) should be considered. One of the possible approaches for improving the overall performance of the TES system is to enhance the thermal properties of the energy storage materials of PW. The current study investigated some of the properties of PW doped with nano-additives, namely, multi-walled carbon nanotubes (MWCNs), forming a nanocomposite PCM. The paraffin/MWCNT composite PCMs were tailor-made for enhanced and efficient TES applications. The thermal storage efficiency of the current TES bed system was approximately 71%, which is significant. Scanning electron spectroscopy (SEM) with energy dispersive X-ray (EDX) characterization showed the physical incorporation of MWCNTs with PW, which was achieved by strong interfaces without microcracks. In addition, the FTIR (Fourier transform infrared) and TGA (thermogravimetric analysis) experimental results of this composite PCM showed good chemical compatibility and thermal stability. This was elucidated based on the observed similar thermal mass loss profiles as well as the identical chemical bond peaks for all of the tested samples (PW, CNT, and PW/CNT composites).

Nanocomposites of silica gel (SG) and multiwalled carbon nanotubes (MWCNTs) of relatively low concentrations (0.25, 0.50, and 0.75 wt%) were characterized before and after annealing. Adsorption is a surface phenomenon, and based on this, the morphology of the composites was investigated by scanning electron microscopy (SEM). The produced images show that the MWCNTs were embedded into the silica gel base material. Fourier transform infrared (FTIR) transmittance spectroscopy showed that MWCNTs were not functionalized within the matrix of silica gel and MWCNT composites. However, after annealing the composites at 400 °C for 4 h in air, evidence of activation was observed in the FTIR spectrum. The effects of the embedding of MWCNTs on porosity, specific surface area, and pore size distribution were studied using Raman spectroscopy. The Raman spectra of the prepared composites were mainly dominated by characteristic sharp scattering peaks of the silica gel at 480, 780, and 990 cm−1 and a broad band centered at 2100 cm−1. The scattering peaks of MWCNTs were not well pronounced, as the homogeneity of the composite is always questionable. Nanosizer analysis showed that at 0.25 wt%, the distribution of MWCNTs within the silica gel was optimal. Vickers hardness measurements showed that the hardness increased with the increasing weight percent of MWCNTs within the composite matrix, while annealing enhanced the mechanical properties of the composites. Further studies are required to investigate the pore structure of silica gel within the matrix of MWCNTs to be deployed for efficient cooling and water purification applications.

The alkylation of benzene with ethylene or propylene to form ethylbenzene (EB) or cumene is an industrially significant transformation. EB is used as an intermediate in the manufacture of styrene, which in turn is an important in the manufacture of many kinds of polymers. The primary use of cumene is in the co-production of phenol and acetone, which in turn are important in the manufacture of many kinds of chemicals and polymers. In industry, EB and cumene are mainly manufactured by the alkylation of benzene with ethene or propene via two methods, the gas and the liquid phase in the presence of Lewis and Brønsted acids. The development of efficient solid catalysts has gained much attention over the last decades. The objective of this chapter is to provide an overview of the history of the alkylation of benzene with ethene and propene, the development of homogeneous and heterogeneous Lewis and Brønsted acids and zeiolite catalysts, the liquid and gas phase alkylation processes, and the industrial technologies for EB and cumene production.