Increased levels of carbon dioxide have revolutionised the Earth; higher temperatures, melting icecaps, and flooding are now more prevalent. Fortunately, renewable energy mitigates this problem by making up 20% of human energy needs. However, from a “green environment” perspective, can carbon dioxide emissions in the atmosphere be reduced and eliminated? The carbon economic circle is an ideal solution to this problem, as it enables us to store, use, and remove carbon dioxide. This research introduces the circular carbon economy (CCE) and addresses its economic importance. Additionally, the paper discusses carbon capture and storage (CCS), and the utilisation of CO₂. Furthermore, it explains current technologies and their future applications on environmental impact, CO₂ capture, utilisation, and storage (CCUS). Various opinions on the best way to achieve zero carbon emissions and on CO₂ applications and their economic impact are also discussed. The circular carbon economy can be achieved through a highly transparent global administration that is supportive of advanced technologies that contribute to the efficient utilisation of energy sources. This global administration must also provide facilities to modernise and develop factories and power stations, based on emission-reducing technologies. Monitoring emissions in countries through a global monitoring network system, based on actual field measurements, linked to a worldwide database allows all stakeholders to track the change in greenhouse gas emissions. The process of sequestering carbon dioxide in the ocean is affected by the support for technologies and industries that adopt the principle of carbon recycling in order to maintain the balance. This includes supporting initiatives that contribute to increasing vegetation cover and preserving oceans from pollutants, especially chemicals and radioactive pollutants, which will undoubtedly affect the process of sequestering carbon dioxide in the oceans, and this will contribute significantly to maintaining carbon dioxide at acceptable levels.

There has been increasing interest in the study and development of nanoparticle-embedded polymeric materials and their applications to special membranes. Nanoparticle-embedded polymeric materials have been observed to have a desirable compatibility with commonly used membrane matrices, a wide range of functionalities, and tunable physicochemical properties. The development of nanoparticle-embedded polymeric materials has shown great potential to overcome the longstanding challenges faced by the membrane separation industry. One major challenge that has been a bottleneck to the progress and use of membranes is the balance between the selectivity and the permeability of the membranes. Recent developments in the fabrication of nanoparticle-embedded polymeric materials have focused on how to further tune the properties of the nanoparticles and membranes to improve the performance of the membranes even further. Techniques for improving the performance of nanoparticle-embedded membranes by exploiting their surface characteristics and internal pore and channel structures to a significant degree have been incorporated into the fabrication processes. Several fabrication techniques are discussed in this paper and used to produce both mixed-matrix membranes and homogenous nanoparticle-embedded polymeric materials. The discussed fabrication techniques include interfacial polymerization, self-assembly, surface coating, and phase inversion. With the current interest shown in the field of nanoparticle-embedded polymeric materials, it is expected that better-performing membranes will be developed soon.

Various carbon dioxide (CO₂) capture materials and processes have been developed in recent years. The absorption-based capturing process is the most significant among other processes, which is widely recognized because of its effectiveness. CO₂ can be used as a feedstock for the production of valuable chemicals, which will assist in alleviating the issues caused by excessive CO₂ levels in the atmosphere. However, the interaction of carbon dioxide with other substances is laborious because carbon dioxide is dynamically relatively stable. Therefore, there is a need to develop types of catalysts that can break the bond in CO₂ and thus be used as feedstock to produce materials of economic value. Metal oxide-based processes that convert carbon dioxide into other compounds have recently attracted attention. Metal oxides play a pivotal role in CO₂ hydrogenation, as they provide additional advantages, such as selectivity and energy efficiency. This review provides an overview of the types of metal oxides and their use for carbon dioxide adsorption and conversion applications, allowing researchers to take advantage of this information in order to develop new catalysts or methods for preparing catalysts to obtain materials of economic value.

High surface area mesoporous polyaniline (M-PANI) films can be produced on the surface of glassy carbon electrodes by the electrochemical polymerization from a composite made by mixing a Brij 98 surfactant with a water solution of aniline and sulfuric acid. The surfactant serves as a structure directing agent. When the quantity of Brij 98 in the composite was 45% by weight, it formed a hexagonal phase that comprises a template of cylinders arranged on a hexagonal lattice with a hydrophilic core. The aniline monomer infiltrated the core of the templates. When the potential of the glassy carbon electrode was cycled, the polymerization occurred inside the hollow core and cast it with the PANI film. Subsequently, the Brij 98 template was removed by a thorough washing with water to produce a well-ordered M-PANI film. The structure and the surface morphology of the M-PANI films were fully characterized by a scanning electron microscope and a transmission electron microscope. The electrochemical capacitance properties were investigated using electrochemical techniques, e.g., cyclic voltammetry, galvanostatic cycling and electrochemical impedance. The data showed a significant increase in the specific capacitance (as high as 532 F g⁻¹) of the M-PANI films when compared with a non M-PANI electrode, which delivered a specific capacitance of 228 F g⁻¹.

The present work is intended to biosynthesize zinc oxide nanoparticles (ZnO NPs) via facile and modern route using aqueous Ziziphus jujuba leaves extract assisted by microwave and explore their photocatalytic degradation of methyl orange anionic dye and methylene blue cationic dye under solar irradiation. The biosynthesized microwave assisted ZnO NPs were characterized and the results showed that ZnO NPs contain hexagonal wurtzite and characterized with a well-defined spherical-like shape with an outstanding band gap (2.70 eV), average particle size of 25 nm and specific surface area of 11.4 m²/g. The photocatalytic degradation of the MO and MB dyes by biosynthesized ZnO NPs under solar irradiation was studied and the results revealed the selective nature of the ZnO NPs for the adsorption and further photocatalytic degradation of the MO dye compared to the MB dye. In addition, the photocatalytic degradation of MO and MB dyes by the ZnO NPs under solar radiation was fitted by the first-order kinetics. Moreover, the photodegradation mechanism proposed that superoxide ions and hydroxyl radicals are the main reactive species.

Nitrogen-doped graphene oxide sheets (N-GOs) are prepared by employing N-containing polymers such as polypyrrole, polyaniline, and copolymer (polypyrrole-polyaniline) doped with acids such as HCl, H₂SO₄, and C₆H₅-SO₃-K, which are activated using different concentrations of KOH and carbonized at 650 °C; characterized using SEM, TEM, BET, TGA-DSC, XRD, and XPS; and employed for the removal of environmental pollutant CO₂. The porosity of the N-GOs obtained were found to be in the range 1–3.5 nm when the KOH employed was in the ratio of 1:4, and the XRD confirmed the formation of the layered like structure. However, when the KOH employed was in the ratio of 1:2, the pore diameter was found to be in the range of 50–200 nm. The SEM and TEM analysis reveal the porosity and sheet-like structure of the products obtained. The nitrogen-doped graphene oxide sheets (N-GOs) prepared by employing polypyrrole doped with C₆H₅-SO₃-K were found to possess a high surface area of 2870 m²/g. The N-GOs displayed excellent CO₂ capture property with the N-GOs; PPy/Ar-1 displayed ~1.36 mmol/g. The precursor employed, the dopant used, and the activation process were found to affect the adsorption property of the N-GOs obtained. The preparation procedure is simple and favourable for the synthesis of N-GOs for their application as adsorbents in greenhouse gas removal and capture.