In this study, ZnAlTi layered double hydroxide (ZnAlTi-LDH) combined with fullerene (C60) was fabricated by the urea method, and calcined under vacuum atmosphere to obtain nanocomposites of C60-modified ZnAlTi layered double oxide (ZnAlTi-LDO). The morphology, structure and composition of the nanocomposites were analyzed by Scanning Electron Microscopy, High-resolution transmission electron microscopy, X-ray diffraction patterns, Fourier transform infrared and specific surface area. The UV-vis diffuse reflectance spectra indicated that the incorporation of C60 expanded the absorption of ZnAlTi-LDO to visible-light region. The photo-degradation experiment was conducted by using a series of C60 modified ZnAlTi-LDO with different C60 weight percentage to degrade Bisphenol A (BPA) under simulated visible light irradiation. In this experiment, the degradation rate of C60 modified ZnAlTi-LDO in photo-degradation of BPA under simulated visible light irradiation was over 80%. The intermediates formed in the degradation of BPA process by using LDO/C60-5% were 4-hydroxyphenyl-2-propanol, 4-isopropenylphenol and Phenol. Photogenerated holes, superoxide radical species, ·OH and singlet oxygen were considered to be responsible for the photodegradation process, among which superoxide radical species and ·OH played a predominant role in the photocatalytic reaction system. C60 modified ZnAlTi-LDO catalysts for photocatalytic reduction shows great potential in degradation of organic pollutants and environmental remediation.

The release assessment of multi-walled carbon nanotubes (CNTs) was performed on two types of polymer-CNT nanocomposites: polypropylene (PP) and polyamide 6 (PA6) containing 3 wt% CNT. Nanocomposite films were prepared and then exposed to ethanol as a fatty-food simulant at 40 °C, and the amount of CNT release into ethanol was determined by ultraviolet–visible spectroscopy (UV–Vis) and graphite furnace atomic absorption spectrometry (GFAAS). The CNTs released into ethanol were visualized by transmission electron microscopy (TEM) and verified by Raman spectroscopy. UV–Vis analysis showed a very small amount of CNT release from the nanocomposite films into ethanol over 60 d: maximum CNT concentrations in ethanol were 1.3 mg/L for the PP-CNT film and 1.2 mg/L for the PA6-CNT film. GFAAS results indicated that the amount of CNTs released into ethanol after 12 d was over 20-fold higher than the results obtained by UV–Vis. Overestimation of CNT release by GFAAS suggested aggregation and poor dispersion of CNTs in the solvent. This assumption was verified by TEM images exhibiting the embedded CNTs in the polymer flakes, which could be poorly dispersed in the solvent. In general, CNT release from the nanocomposite films was considered a surface phenomenon, as indicated by detachment of CNT-containing polymer flakes from the film surface.

This study describes the immobilization of ginger peroxidase on amino-functionalized silica-coated titanium dioxide nanocomposite and its application in bioremediation process. A dramatic enhancement in enzyme activity was observed after immobilization on nanosupport which was evident from the effectiveness factor (η) value of 1.76. Immobilization of enzyme on nanosupport was confirmed by transmission electron microscopy, scanning electron microscopy, and Fourier transform infrared spectroscopy. Immobilized peroxidase exhibited higher activity in a broad range of pH and temperature as compared to free enzyme. Also, the thermostability of peroxidase was strikingly improved upon immobilization. After six repeated uses, the immobilized peroxidase retained around 62% of its dye decolorization activity. V ₘₐₓ of the enzyme was changed to 35.01 μmol L⁻¹ min⁻¹ from 8.42 μmol L⁻¹ min⁻¹ after immobilization on nanocomposite, which was a fourfold increase as compared to the free enzyme. Circular dichroism spectroscopy demonstrated conformational changes in the secondary structure of the enzyme, a possible reason for the enhanced enzyme activity after immobilization. Immobilized peroxidase was highly efficient in the removal of acid yellow 42 dye in a stirred batch process, i.e., 90% of the dye was decolorized within 1.5 h as compared to the free enzyme decolorizing only 69% of the dye in the same period. Our results clearly demonstrate that this nanobioconjugate with enhanced catalytic activity, high stability, and very good reusability has remarkable potential for the treatment of aromatic pollutants present in wastewater. Graphical Abstract Schematic representation of immobilization of ginger peroxidase on amino functionalized silica coated titanium dioxide nanocomposite and its use in dye decolorization process.

Mercury (Hg) is an environmental pollutant which is detrimental to the health of living beings due to the toxicity in its all oxidation states. To control mercury pollution development of low cost, efficient and highly sensitive prototype mercury sensor remains a challenge. In the present work, we have proposed a low-cost prototype device based on silver nanoparticle-impregnated poly(vinyle alcohol) (PVA-Ag-NPs) nanocomposite thin film for mercury detection. The thin film, fabricated through a facile protocol, is shown to be a fast, efficient, and selective sensor for Hg²⁺ in aqueous medium with a detection limit of 10 ppb. We have utilized the aggregation and amalgamation of Ag-NPs with Hg²⁺ to develop the low-cost, highly efficient and feasible prototype mercury sensor. In the presence of Hg²⁺, the yellowish thin film turned into colourless due to the loss of intense surface plasmon resonance (SPR) absorption band of the silver nanoparticles (Ag-NPs) through aggregation and amalgamation with mercury. The developed sensor has high selectivity for Hg²⁺ ions over a wide range of other competing heavy metal ions, generally present in water of natural sources. The sensor response is found to be linear over the Hg²⁺ ion concentration regime from 10 ppb to 5 ppm. The developed sensor has shown to determine a trace Hg²⁺ ions in real water samples. Finally, using the proposed technique, we have developed a simple and inexpensive prototype device for monitoring in field environmental mercury pollution. Graphical Abstract ᅟ

Fe₃O₄ decorated multi-walled carbon nanotube (Fe₃O₄/MWCNT) nanocomposites were synthesized by co-precipitation process and used as heterogeneous Fenton catalyst for degradation of phenol and p-nitrophenol (p-NP). The Fe₃O₄ nanoparticles with size less than 20 nm were well-dispersedly coated on the surface of MWCNTs at relatively low loading. Some aggregations appear at high Fe₃O₄ content in composite. The Fe₃O₄/MWCNT with about 25 wt.% of Fe₃O₄ is the most cost-effective catalyst compared with others, whose phenol conversion and COD removal rates could, respectively, reach to 99.20 and 58.09%. And a high H₂O₂ utilization efficiency was achieved (about 132.41%) for this catalyst. For the p-NP degradation, the optimal reaction condition was that: 2.0 mg/L of catalyst dosage, 3 mmol/L of initial H₂O₂ concentration, 3 of pH value, and 40 °C of reaction temperature. At this condition, the removal rates of p-NP and COD in 120 min achieved 97.16 and 67.71%, respectively. And the Fe₃O₄/MWCNT nanocomposite also exhibits an acceptable stability and reusability.

A novel quaternary nanocomposites consisting of Ag/AgCl decorated TiO₂ introduced on graphene oxide (GO) sheets with high loading of GO (50 wt.%) were prepared for photocatalytic application. The composite powders were synthesized by a facile sol–gel method utilizing polyvinylpyrrolidone (PVP) as a reducing agent to obtain Ag particles and a modified Hummers’ method to acquire GO sheets. The influence of reducing agent concentration and type of TiO₂ was investigated. The adsorption properties of the GO/TiO₂/Ag/AgCl nanocomposites were examined, and photocatalytic activity was investigated under UV light applying methylene blue (MB) as a model pollutant. The composites displayed great adsorption capability up to 112.6 mgg⁻¹ due to GO. It is shown that the GO/TiO₂/Ag/AgCl samples prepared by Degussa P25 TiO₂ and with a reduced amount of PVP have the best photocatalytic activity, reaching up to 55% decolorization of methylene blue under UV light. The photocatalytic activity is enhanced by approximately 80% with the addition of GO to the quaternary GO/TiO₂/Ag/AgCl composites.

Graphene oxide (GO) and graphene oxide modified with methyl-β-cyclodextrin denoted as GO-mβCD were prepared and applied as adsorbents to determine the adsorption characteristics of Pb(II) from aqueous solutions. The characteristic results of Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), Raman spectroscopy, and scanning electron microscopy (SEM) showed that mβCD was successfully physically attached to GO to form the GO-mβCD nanocomposite. The adsorption equilibrium and kinetics of the adsorbents were well described by Langmuir isotherm and pseudo-second-order models, respectively. The maximum Pb(II) adsorption capacity of GO-mβCD (at pH = 6 and room temperature) was determined as 312.5 mg/g which was significantly higher than that of GO (217.39 mg/g). This indicates that the modification of GO with mβCD enhances the adsorption capacity of GO. The desorption studies show that the adsorbent GO-mβCD can be used for at least five cycles with non-significant loss of its initial adsorption capacity for Pb(II) ions.

In this study, an iron oxide-coated zeolite (IOCZ) nanocomposite was synthesized and used for the removal of U(VI) and As(III) from aqueous solutions using a batch system. Parameters such as various contact times, pH, competing ions (Cd²⁺, Co²⁺, and Cr³⁺), temperature, and initial concentrations of uranium(VI) and arsenic(III) were investigated. The experimental results were fitted to the Langmuir, Freundlich, and Dubinin–Radushkevich isotherms to obtain the characteristic parameters of each model. Results suggested that adsorption of U(VI) and As(III) by IOCZ was best modeled with the Freundlich isotherm. The kinetic experimental data fitted the pseudo second-order model better than the pseudo first-order model for both elements. Using the thermodynamic equilibrium constants obtained at different temperatures, various thermodynamic parameters, such as ΔG ᵒ, ΔH ᵒ, and ΔS ᵒ, were calculated. These parameters indicated that the process is spontaneous and exothermic in nature. It was noted that an increase in temperature resulted in a decrease of 8.5 and 27.5% for U and As removal, respectively. An increase in initial concentrations of U(VI) and As(III) from 10 to 100 mg L⁻¹ at pH 3 resulted in increased adsorption capacities (q ₑ) for both elements. The increases were from 1.247 to 20.10 mg g⁻¹ for U(VI) and from 3.115 to 54.18 mg g⁻¹ for As(V). The presence of competing ions such as Cd²⁺, Co²⁺, and Cr³⁺ enhanced the removal of As by 9.2% whereas the adsorption capacity of uranium decreased by 13.8%. This research demonstrated that IOCZ is a potential adsorbent for the removal of U(VI) and As(III) from aqueous solutions.

In this article, Cr(OH)₃ nanoparticle-modified cellulose nanocrystal (CNC) as a novel hybrid nanocomposite (Cr(OH)₃-NPs-CNC) was prepared by a simple procedure and used as a sorbent for adsorptive removal of methylene blue (MB) and malachite green (MG) from aqueous solution. Different kinetic models were tested, and the pseudo-second-order kinetic model was found more suitable for the MB and MG adsorption processes. The BET and Langmuir models were more suitable for the adsorption processes of MB and MG. Thermodynamic studies suggested that the adsorption of MB and MG onto Cr(OH)₃-NPs-CNC nanocomposite was a spontaneous and endothermic process. The maximum adsorption capacities for MB and MG were reached 106 and 104 mg/g, respectively, which were almost two times higher than unmodified CNC. The chemical stability and leaching tests of the Cr(OH)₃-NPs-CNC hybrid nanocomposite showed that only small amounts of chromium were leached into the solution.

The applications of multilayered graphenes (MLGs), nanocomposites “MLG–decontaminant” and polydicarbonfluoride intercalation compounds for the localization and deactivation of toxic spills and gaseous emissions under technogenic accidents are investigated in this paper. The intercalation compounds contain oxidizers as intercalants, and MLGs are formed destructively by thermolysis of polydicarbonfluoride intercalation compounds. The sorptive capacity of MLGs (about 240 ml of liquid phase per 1 g of MLG) is much higher than in well-known expanded graphites (EGs) obtained from graphite oxide or graphite acid salts. Our investigation revealed the possibility of the production of the “MLG–decontaminant” nanocomposites with the neutralizator content >95% due to the extremely low (down to 0.4 g/l) apparent density of MLG and its high specific surface (about 370 m²/g). The use of these nanocomposites for the acid–base or redox neutralization of contaminants does not result in the overheating, sputtering or evaporation of liquid phases, because their neutralization products sorb into MLGs. It prevents the soil mineralization by liquid or solid deactivated spills. We revealed that polydicarbonfluoride intercalation compounds with oxidizers (ClF₃, HNO₃, N₂O₄) can be efficiently used for the deactivation of spills and gaseous emissions of nitrogen-containing base compounds.